WO2008085332A2 - Nonwovens fabrics produced from multicomponent fibers comprising sulfopolyesters - Google Patents
Nonwovens fabrics produced from multicomponent fibers comprising sulfopolyesters Download PDFInfo
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- WO2008085332A2 WO2008085332A2 PCT/US2007/025770 US2007025770W WO2008085332A2 WO 2008085332 A2 WO2008085332 A2 WO 2008085332A2 US 2007025770 W US2007025770 W US 2007025770W WO 2008085332 A2 WO2008085332 A2 WO 2008085332A2
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Classifications
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/435—Polyesters
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/04—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers
- D01F8/14—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from synthetic polymers with at least one polyester as constituent
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4282—Addition polymers
- D04H1/4291—Olefin series
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/4334—Polyamides
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4326—Condensation or reaction polymers
- D04H1/4358—Polyurethanes
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
- D04H1/43825—Composite fibres
- D04H1/43828—Composite fibres sheath-core
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
- D04H1/43825—Composite fibres
- D04H1/4383—Composite fibres sea-island
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
- D04H1/4382—Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
- D04H1/43838—Ultrafine fibres, e.g. microfibres
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/44—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling
- D04H1/46—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres
- D04H1/48—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres in combination with at least one other method of consolidation
- D04H1/49—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres in combination with at least one other method of consolidation entanglement by fluid jet in combination with another consolidation means
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/44—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling
- D04H1/46—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres
- D04H1/492—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties the fleeces or layers being consolidated by mechanical means, e.g. by rolling by needling or like operations to cause entanglement of fibres by fluid jet
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- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H3/00—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
- D04H3/08—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
- D04H3/10—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between yarns or filaments made mechanically
- D04H3/11—Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between yarns or filaments made mechanically by fluid jet
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/637—Including strand or fiber material which is a monofilament composed of two or more polymeric materials in physically distinct relationship [e.g., sheath-core, side-by-side, islands-in-sea, fibrils-in-matrix, etc.] or composed of physical blend of chemically different polymeric materials or a physical blend of a polymeric material and a filler material
- Y10T442/641—Sheath-core multicomponent strand or fiber material
Definitions
- the present invention pertains to processes to produce nonwoven fabrics from multicomponent fibers wherein the multicomponent fibers comprise at least one water-dispersible sulfopolyester and at least one water non-dispersible polymer.
- Nonwoven fabrics are similar to woven and knitted fabrics in that both are planar, inherently flexible, porous structures composed of polymer-based materials. The main difference between the two is the process in which the fabric is made.
- Woven fabrics are made by interlacing two or more sets of yarns at right angles to one another in a designated order.
- Nonwoven fabrics are made by placing a predetermined number of fibers or filaments into a two-dimentional array and locking them together.
- the nonwoven fabric can be assembled by mechanically, chemically, or thermally interlocking layers or networks of fibers, filaments or yarns.
- processes for producing nonwoven fabrics can be grouped into four general classifications: textile, paper, extrusion, and hybrid, meaning a combination of these technologies are utilized.
- Extrusion technology is used to produce spunbond, meltblown, and porous- film nonwovens. These types of nonwovens are sometimes called polymer-laid nonwovens.
- Spunbond and meltblown processes are an advancement in the production of nonwovens fabrics since the nonwovens are made directly from the materials used to make the fibers themselves, thus eliminating the fiber production step.
- the spunbond process tranforms polymer directly to fabric by extruding filaments, orienting them as bundles or groupings, layering them on a conveying screen, and interlocking them by thermal fusion, mechanical entanglement, chemical adhesives, or combinations of these methods.
- Nonwovens are utilized in textile applications such as, for example, clothing, curtains, upholstery, and uniforms.
- Nonwoven fabrics can also be utilized in personal care products, such as, but not limited to, wipes, feminine hygiene products, baby diapers, adult incontinence briefs, and hospital/surgical and other medical disposables.
- Other applications include, but are not limited to, protective fabrics and layers, geotextiles, industrial wipes, and filter media.
- This invention provides novel processes to produce nonwoven fabrics from multicomponent fibers comprising at least one water dispersible sulfopolyester and at least one water non-dispersible polymers.
- a process for making a nonwoven fabric comprises: (A) collecting multicomponent fibers to form a non-woven web; wherein the multicomponent fiber comprises at least one water dispersible sulfopolyester and at least one water non-dispersible polymer; wherein the multicomponent fiber has a plurality of domains comprising the water non- dispersible polymer; wherein the domains are substantially isolated from each other by the water dispersible sulfopolyester intervening between the domains; (B) contacting the non-woven web with water at a sufficient temperature and pressure to remove a portion of the water dispersible sulfopolyester thereby forming a microfiber web; and (C) hydroentangling the microfiber web to produce the nonwoven fabric.
- another process for making a nonwoven fabric comprises: (A) collecting the multicomponent fibers to form a non-woven web; wherein the multicomponent fiber comprises at least one water dispersible sulfopolyester and at least one water non- dispersible polymer; wherein the multicomponent fiber has a plurality of domains comprising the water non-dispersible polymer; wherein the domains are substantially isolated from each other by the water dispersible sulfopolyester intervening between the domains; and (B) contacting the non-woven web with water at a sufficient temperature and pressure to remove a portion of the water dispersible sulfopolyester thereby forming microfibers and simultaneously hydroentangling the microfibers to produce the nonwoven fabric.
- Our invention thus offers a novel and inexpensive process to produce nonwoven fabric.
- the nonwoven fabric may be in the form of a flat fabric or a 3- dimensional shape and may be incorporated into a variety of fibrous articles such as those discuss
- Figure 1 illustrates the sponbond process.
- Figure 2 illustrates how the examples relate to one another.
- Ranges may be expressed herein as from “about” one particular value, and/or to "about” another particular value. When such a range is expressed, another embodiment includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent "about,” it will be understood that the particular value forms another embodiment. It will be further understood that the endpoints of each of the ranges are significant both in relation to the other endpoint, and independently of the other endpoint. Further, the ranges stated in this disclosure and the claims are intended to include the entire range specifically and not just the endpoint(s).
- a range stated to be 0 to 10 is intended to disclose all whole numbers between 0 and 10 such as, for example 1, 2, 3, 4, etc., all fractional numbers between 0 and 10, for example 1.5, 2.3, 4.57, 6.1113, etc., and the endpoints 0 and 10.
- a range associated with chemical substituent groups such as, for example, "Cl to C5 hydrocarbons”, is intended to specifically include and disclose Cl and C5 hydrocarbons as well as C2, C3, and C4 hydrocarbons.
- nonwoven fabric or “nonwoven web” means a structure of individual fibers or threads which are interlaid, but not in an identifiable manner as in a knitted fabric.
- the basis weight of nonwoven fabrics is usually expressed in ounces of material per square yard (osy) or grams per square meter (gsm).
- fiber refers to an elongated extrudate formed by passing a polymer through a forming orifice such as a die. Unless noted as otherwise the term “fibers” include discontinuous strands having a definite length and continuous strands of material, such as filaments.
- the nonwoven fabric of the present invention may be formed from staple multicomponent fibers. Such staple fibers may be carded and bonded to form the nonwoven fabric. Desirably, however, the nonwoven fabric of the present invention is made with continuous multicomponent filaments which are extruded, drawn, and laid on a traveling forming surface.
- the microfibers utilized to produce the nonwoven fabric of this invention typically have d/f values of 1 or less, 0.5 or less, or 0.1 or less.
- multicomponent fibers or “conjugate fibers” refers to fibers which have been formed from at least two polymer components. Such fibers are usually extruded from separate extruders but spun together to form one fiber.
- the polymers of the respective components are usually different from each other although multicomponent fibers may comprise separate components of similar or identical polymeric materials.
- the individual components are typically arranged in substantially constantly positioned distinct segments or zones across the cross-section of the multicomponent fiber and extend substantially along the entire length of the multicomponent fiber.
- the configuration of such multicomponent fibers may be, for example, a side by side arrangement, a pie arrangement or other arrangement. Multicomponent fibers and methods of making the same are taught in U.S. Pat. No.
- polymer generally includes, but is not limited to, homopolymers, copolymers, such as for example, block, graft, random and alternating copolymers, terpolymers, etc., and blends and modifications thereof.
- polymer shall include all possible geometric configurations of the molecules. These configurations include, but are not limited to, isotactic, syndiotactic and random symmetries.
- water-dispersible as used herein in reference to the water dispersible sulfopolyester as one component of a multicomponent fiber, is intended to be synonymous with the terms “water-dissipatable”, “water-disintegratable”, “water- dissolvable”, “water-dispellable”, “water soluble”, “water-removable”, “hydro- soluble”, and “hydrodispersible” and is intended to mean that the sulfopolyester component is sufficiently removed from the multicomponent fiber and is dispersed or dissolved by the action of water to enable the release and separation of the water non- dispersible polymer fibers contained therein.
- dispersible means that, using a sufficient amount of deionized water (e.g., 100:1 wate ⁇ fiber by weight) to form a loose suspension or slurry of the fibers, at a temperature of about 6O 0 C, and within a time period of up to 5 days, the sulfopolyester component dissolves, disintegrates, or separates from the multicomponent fiber, leaving behind a plurality of microfibers from the water non- dispersible polymer segments.
- a sufficient amount of deionized water e.g., 100:1 wate ⁇ fiber by weight
- all of these terms refer to the activity of water or a mixture of water and a water-miscible cosolvent on the water dispersible sulfopolyesters described herein.
- water-miscible cosolvents include, but are not limited to, alcohols, ketones, glycol ethers, esters and the like. It is intended for this terminology to include conditions where the water dispersible sulfopolyester is dissolved to form a true solution as well as those where the water dispersible sulfopolyester is dispersed within the aqueous medium.
- segment or “domain” or “zone” when used to describe the shaped cross section of a multicomponent fiber refers to the area within the cross section comprising the water non-dispersible polymers where these domains or segments are substantially isolated from each other by the water-dispersible sulfopolyester intervening between the segments or domains.
- segment or domains are set apart from each other to permit the segments domains to form individual fibers upon removal of the sulfopolyester.
- Segments or domains or zones can be of similar size and shape or varying size and shape. Again, segments or domains or zones can be arranged in any configuration. These segments or domains or zones are “substantially continuous” along the length of the multicomponent extrudate or fiber. The term “substantially continuous” means continuous along at least a 10 cm length of the multicomponent fiber.
- the present invention provides processes to produce nonwoven fabrics from multicomponent fibers wherein the multicomponent fibers comprise at least one water-dispersible sulfopolyester and at least one water non-dispersible polymer.
- a process comprising: (A) collecting multicomponent fibers to form a non- woven web; wherein the multicomponent fiber comprises at least one water dispersible sulfopolyester and at least one water non- dispersible polymer; wherein the multicomponent fiber has a plurality of domains comprising the water non-dispersible polymer; wherein the domains are substantially isolated from each other by the water dispersible sulfopolyester intervening between the domains; (B) contacting the non- woven web with water at a sufficient temperature and pressure to remove a portion of the water dispersible sulfopolyester thereby forming a microf ⁇ ber web; and (C) hydroentangling the microfiber web to produce the nonwoven fabric.
- the multicomponent fibers of our invention can be prepared by melt spinning a single sulfopolyester or sulfopolyester blend with the water non-dispersible polymer immiscible with the sulfopolyester.
- a multicomponent fiber is prepared by extruding the sulfopolyester and one or more water non-dispersible polymers, which are immiscible with the sulfopolyester, separately through a spinneret having a shaped or engineered transverse geometry such as, for example, an "islands-in-the-sea", sheath-core, side-by-side, or segmented pie configuration.
- the water dispersible sulfopolyester is later removed by dissolving the interfacial layers or pie segments and leaving the smaller filaments or microfibers of the water non-dispersible polymer(s). These fibers of the water non-dispersible polymer have fiber size much smaller than the multicomponent fiber before removing the water dispersible sulfopolyester.
- the multicomponent fiber is produced by feeding the sulfopolyester and water non-dispersible polymers to a polymer distribution system where the polymers are introduced into a segmented spinneret plate.
- the polymers follow separate paths to the fiber spinneret and are combined at the spinneret hole which comprises either two concentric circular holes thus providing a sheath-core type fiber, or a circular spinneret hole divided along a diameter into multiple parts to provide a fiber having a side-by-side type.
- the immiscible water dispersible sulfopolyester and water non-dispersible polymers may be introduced separately into a spinneret having a plurality of radial channels to produce a multicomponent fiber having a segmented pie cross section.
- the sulfopolyester will form the "sheath" component of a sheath core configuration.
- the water non-dispersible segments typically, are substantially isolated from each other by the sulfopolyester.
- multicomponent fibers may be formed by melting the sulfopolyester and water non-dispersible polymers in separate extruders and directing the polymer flows into one spinneret with a plurality of distribution flow paths in form of small thin tubes or segments to provide a multicomponent fiber having an islands-in-the-sea shaped cross section.
- a spinneret is described in U.S. Patent No. 5,366,804, herein incorporated by reference to the extent it does not contradict the statements herein.
- the sulfopolyester will form the "sea" component and the water non-dispersible polymer will form the "islands" component.
- the shaped cross section of a multicomponent fiber can, for example, be in the form of a sheath core, islands-in-the sea, segmented pie, hollow segmented pie; off-centered segmented pie, etc.
- the multicomponent fiber of the present invention is prepared from polyesters or, more specifically sulfopolyesters, comprising dicarboxylic acid monomer residues, sulfomonomer residues, diol monomer residues, and repeating units.
- the sulfomonomer may be a dicarboxylic acid, a diol, or hydroxycarboxylic acid.
- the term "monomer residue”, as used herein, means a residue of a dicarboxylic acid, a diol, or a hydroxycarboxylic acid.
- a “repeating unit”, as used herein, means an organic structure having 2 monomer residues bonded through a carbonyloxy group.
- the sulfopolyesters of the present invention contain substantially equal molar proportions of acid residues (100 mole %) and diol residues (100 mole %) which react in substantially equal proportions such that the total moles of repeating units is equal to 100 mole %.
- the mole percentages provided in the present disclosure therefore, may be based on the total moles of acid residues, the total moles of diol residues, or the total moles of repeating units.
- a sulfopolyester containing 30 mole% of a sulfomonomer, which may be a dicarboxylic acid, a diol, or hydroxycarboxylic acid, based on the total repeating units means that the sulfopolyester contains 30 mole% sulfomonomer out of a total of 100 mole% repeating units. Thus, there are 30 moles of sulfomonomer residues among every 100 moles of repeating units.
- a sulfopolyester containing 30 mole% of a dicarboxylic acid sulfomonomer, based on the total acid residues means the sulfopolyester contains 30 mole% sulfomonomer out of a total of 100 mole% acid residues.
- the sulfopolyesters described herein have an inherent viscosity, abbreviated hereinafter as "Ih.V.”, of at least about 0.1 dL/g measured in a 60/40 parts by weight solution of phenol/tetrachloroethane solvent at 25 0 C and at a concentration of about 0.5 g of sulfopolyester in 100 mL of solvent.
- the inherent viscosity of the sulfopolyester can also range from about 0.2 to about 0.3 dL/g. Another range for inherent viscosity is greater than about 0.3 dL/g.
- polystyrene resin encompasses both “homopolyesters” and “copolyesters” and means a synthetic polymer prepared by the polycondensation of difunctional carboxylic acids with difunctional hydroxyl compound.
- sulfopolyester means any polyester comprising a sulfomonomer.
- the difunctional carboxylic acid is a dicarboxylic acid and the difunctional hydroxyl compound is a dihydric alcohol such as, for example glycols and diols.
- the difunctional carboxylic acid may be a hydroxy carboxylic acid such as, for example, p-hydroxybenzoic acid
- the difunctional hydroxyl compound may be an aromatic nucleus bearing 2 hydroxy substituents such as, for example, hydroquinone.
- the term "residue”, as used herein, means any organic structure incorporated into the polymer through a polycondensation reaction involving the corresponding monomer.
- the dicarboxylic acid residue may be derived from a dicarboxylic acid monomer or its associated acid halides, esters, salts, anhydrides, or mixtures thereof.
- dicarboxylic acid is intended to include dicarboxylic acids and any derivative of a dicarboxylic acid, including its associated acid halides, esters, half-esters, salts, half-salts, anhydrides, mixed anhydrides, or mixtures thereof, useful in a polycondensation process with a diol to make a high molecular weight polyester.
- the sulfopolyester of the present invention includes one or more dicarboxylic acid residues.
- the dicarboxylic acid residue may comprise from about 60 to about 100 mole% of the acid residues.
- concentration ranges of dicarboxylic acid residues are from about 60 mole% to about 95 mole%, and about 70 mole% to about 95 mole%.
- dicarboxylic acids that may be used include aliphatic dicarboxylic acids, alicyclic dicarboxylic acids, aromatic dicarboxylic acids, or mixtures of two or more of these acids.
- suitable dicarboxylic acids include, but are not limited to, succinic; glutaric; adipic; azelaic; sebacic; fumaric; maleic; itaconic; 1,3-cyclohexanedicarboxylic; 1 ,4-cyclohexanedicarboxylic; diglycolic; 2,5- norbornanedicarboxylic; phthalic; terephthalic; 1,4-naphthalenedicarboxylic; 2,5- naphthalenedicarboxylic; diphenic; 4,4'-oxydibenzoic; 4,4'-sulfonyidibenzoic; and isophthalic.
- the preferred dicarboxylic acid residues are isophthalic, terephthalic, and 1 ,4-cyclohexanedicarboxylic acids, or if diesters are used, dimethyl terephthalate, dimethyl isophthalate, and dimethyl- 1,4-cyclohexanedicarboxylate.
- dicarboxylic acid methyl ester can be utilized, it is also acceptable to include higher order alkyl esters, such as ethyl, propyl, isopropyl, butyl, and so forth.
- aromatic esters particularly phenyl, also may be employed.
- the sulfopolyester includes about 4 to about 40 mole%, based on the total repeating units, of residues of at least one sulfomonomer having 2 functional groups and one or more sulfonate groups attached to an aromatic or cycloaliphatic ring wherein the functional groups are hydroxyl, carboxyl, or a combination thereof. Additional examples of concentration ranges for the sulfomonomer residues are about 4 to about 35 mole%, about 8 to about 30 mole%, and about 8 to about 25 mole%, based on the total repeating units.
- the sulfomonomer may be a dicarboxylic acid or ester thereof containing a sulfonate group, a diol containing a sulfonate group, or a hydroxy acid containing a sulfonate group.
- sulfonate refers to a salt of a sulfonic acid having the structure "-SO 3 M" wherein M is the cation of the sulfonate salt.
- the cation of the sulfonate salt may be a metal ion such as Li + , Na + , K + , Mg ++ , Ca "1"1" , Ni +"1” , Fe + *, and the like.
- the cation of the sulfonate salt may be non-metallic such as a nitrogenous base as described, for example, in U.S. Patent No. 4,304,901.
- Nitrogen-based cations are derived from nitrogen-containing bases, which may be aliphatic, cycloaliphatic, or aromatic compounds. Examples of such nitrogen containing bases include ammonia, dimethylethanolamine, diethanolamine, triethanolamine, pyridine, morpholine, and piperidine.
- the method of this invention for preparing sulfopolyesters containing nitrogen-based sulfonate salt groups is to disperse, dissipate, or dissolve the polymer containing the required amount of sulfonate group in the form of its alkali metal salt in water and then exchange the alkali metal cation for a nitrogen-based cation.
- the resulting sulfopolyester is completely dispersible in water with the rate of dispersion dependent on the content of sulfomonomer in the polymer, temperature of the water, surface area/thickness of the sulfopolyester, and so forth.
- a divalent metal ion is used, the resulting sulfopolyesters are not readily dispersed by cold water but are more easily dispersed by hot water. Utilization of more than one counterion within a single polymer composition is possible and may offer a means to tailor or fine-tune the water-responsivity of the resulting article of manufacture.
- sulfomonomers residues include monomer residues where the sulfonate salt group is attached to an aromatic acid nucleus, such as, for example, benzene; naphthalene; diphenyl; oxydiphenyl; sulfonyldiphenyl; and methylenediphenyl or cycloaliphatic rings, such as, for example, cyclohexyl; cyclopentyl; cyclobutyl; cycloheptyl; and cyclooctyl.
- aromatic acid nucleus such as, for example, benzene; naphthalene; diphenyl; oxydiphenyl; sulfonyldiphenyl; and methylenediphenyl or cycloaliphatic rings, such as, for example, cyclohexyl; cyclopentyl; cyclobutyl; cycloheptyl; and cyclooctyl.
- sulfomonomer residues which may be used in the present invention are the metal sulfonate salt of sulfophthalic acid, sulfoterephthalic acid, sulfoisophthalic acid, or combinations thereof.
- sulfomonomers which may be used are 5-sodiosulfoisophthalic acid and esters thereof. If the sulfomonomer residue is from 5-sodiosulfoisophthalic acid, typical sulfomonomer concentration ranges are about 4 to about 35 mole%, about 8 to about 30 mole %, and about 8 to 25 mole %, based on the total moles of acid residues.
- the sulfomonomers used in the preparation of the sulfopolyesters are known compounds and may be prepared using methods well known in the art.
- sulfomonomers in which the sulfonate group is attached to an aromatic ring may be prepared by sulfonating the aromatic compound with oleum to obtain the corresponding sulfonic acid and followed by reaction with a metal oxide or base, for example, sodium acetate, to prepare the sulfonate salt.
- Procedures for preparation of various sulfomonomers are described, for example, in U.S. Patent No.'s 3,779,993; 3,018,272; and 3,528,947.
- polyester using, for example, a sodium sulfonate salt, and ion-exchange methods to replace the sodium with a different ion, such as zinc, when the polymer is in the dispersed form.
- a sodium sulfonate salt and ion-exchange methods to replace the sodium with a different ion, such as zinc, when the polymer is in the dispersed form.
- This type of ion exchange procedure is generally superior to preparing the polymer with divalent salts insofar as the sodium salts are usually more soluble in the polymer reactant melt-phase.
- the sulfopolyester includes one or more diol residues which may include aliphatic, cycloaliphatic, and aralkyl glycols.
- the cycloaliphatic diols for example, 1,3- and 1,4-cyclohexanedimethanol, may be present as their pure cis or trans isomers or as a mixture of cis and trans isomers.
- diol is synonymous with the term "glycol” and means any dihydric alcohol.
- diols include, but are not limited to, ethylene glycol; diethylene glycol; Methylene glycol; polyethylene glycols; 1,3 -propanediol; 2,4-dimethyl-2-ethylhexane-l,3-diol; 2, 2-dimethyl- 1,3 -propanediol; 2-ethyl-2-butyl-l,3-propanediol; 2-ethyl-2-isobutyl- 1,3-propanediol; 1,3-butanediol; 1,4-butanediol; 1,5-pentanediol; 1,6-hexanediol; 2,2,4-trimethyl-l,6-hexanediol; thiodiethanol; 1,2-cyclohexanedimethanol; 1,3- cyclohexanedimethanol; 1 ,4-cyclohexanedimethanol; 2,2,4-cycl
- n is an integer in the range of 2 to about 500.
- lower molecular weight polyethylene glycols e.g., wherein n is from 2 to 6, are diethylene glycol, triethylene glycol, and tetraethylene glycol. Of these lower molecular weight glycols, diethylene and triethylene glycol are preferred.
- Higher molecular weight polyethylene glycols (abbreviated herein as "PEG"), wherein n is from 7 to about 500, include the commercially available products known under the designation CARBOWAX®, a product of Dow Chemical Company (formerly Union Carbide).
- PEGs are used in combination with other diols such as, for example, diethylene glycol or ethylene glycol.
- diols such as, for example, diethylene glycol or ethylene glycol.
- the molecular weight may range from greater than 300 to about 22,000 g/mol.
- the molecular weight and the mole% are inversely proportional to each other; specifically, as the molecular weight is increased, the mole % will be decreased in order to achieve a designated degree of hydrophilicity.
- a PEG having a molecular weight of 1000 may constitute up to 10 mole% of the total diol, while a PEG having a molecular weight of 10,000 would typically be incorporated at a level of less than 1 mole% of the total diol.
- Certain dimer, trimer, and tetramer diols may be formed in situ due to side reactions that may be controlled by varying the process conditions. For example, varying amounts of diethylene, triethylene, and tetraethylene glycols may be formed from ethylene glycol from an acid-catalyzed dehydration reaction which occurs readily when the polycondensation reaction is carried out under acidic conditions.
- buffer solutions well-known to those skilled in the art, may be added to the reaction mixture to retard these side reactions. Additional compositional latitude is possible, however, if the buffer is omitted and the dimerization, trimerization, and tetramerization reactions are allowed to proceed.
- the sulfopolyester of the present invention may include from 0 to about 25 mole%, based on the total repeating units, of residues of a branching monomer having 3 or more functional groups wherein the functional groups are hydroxyl, carboxyl, or a combination thereof.
- branching monomers are 1,1,1- trimethylol propane, 1,1,1-trimethylolethane, glycerin, pentaerythritol, erythritol, threitol, dipentaerythritol, sorbitol, trimellitic anhydride, pyromellitic dianhydride, dimethylol propionic acid, or combinations thereof.
- branching monomer concentration ranges are from 0 to about 20 mole% and from 0 to about 10 mole%.
- the presence of a branching monomer may result in a number of possible benefits to the sulfopolyester of the present invention, including but not limited to, the ability to tailor rheological, solubility, and tensile properties.
- a branched sulfopolyester compared to a linear analog, will also have a greater concentration of end groups that may facilitate post- polymerization crosslinking reactions.
- branching agent At high concentrations of branching agent, however, the sulfopolyester may be prone to gelation.
- the sulfopolyester used for the multicomponent fiber of the present invention has a glass transition temperature, abbreviated herein as "Tg", of at least 25 0 C as measured on the dry polymer using standard techniques, such as differential scanning calorimetry ("DSC"), well known to persons skilled in the art.
- Tg measurements of the sulfopolyesters of the present invention are conducted using a "dry polymer", that is, a polymer sample in which adventitious or absorbed water is driven off by heating to polymer to a temperature of about 200 0 C and allowing the sample to return to room temperature.
- the sulfopolyester is dried in the DSC apparatus by conducting a first thermal scan in which the sample is heated to a temperature above the water vaporization temperature, holding the sample at that temperature until the vaporization of the water absorbed in the polymer is complete (as indicated by an a large, broad endotherm), cooling the sample to room temperature, and then conducting a second thermal scan to obtain the Tg measurement.
- Further examples of glass transition temperatures exhibited by the sulfopolyester are at least 3O 0 C, at least 35 0 C, at least 4O 0 C, at least 5O 0 C, at least 6O 0 C, at least 65 0 C, at least 8O 0 C, and at least 9O 0 C.
- typical glass transition temperatures of the dry sulfopolyesters in our invention are about 3O 0 C, about 48 0 C, about 55 0 C, about 65 0 C, about 7O 0 C, about 75 0 C, about 85 0 C, and about 9O 0 C.
- the sulfopolyesters of this invention may be a single polyester or may be blended with one or more supplemental polymers to modify the properties of the resulting multicomponent fiber.
- the supplemental polymer may or may not be water-dispersible depending on the application and may be miscible or immiscible with the sulfopolyester. If the supplemental polymer is water non-dispersible, it is preferred that the blend with the sulfopolyester is immiscible.
- miscible as used herein, is intended to mean that the blend has a single, homogeneous amorphous phase as indicated by a single composition- dependent Tg.
- a first polymer that is miscible with second polymer may be used to "plasticize" the second polymer as illustrated, for example, in U.S. Patent No. 6,211,309.
- the term "immiscible”, as used herein denotes a blend that shows at least 2, randomly mixed, phases and exhibits more than one Tg.
- Some polymers may be immiscible and yet compatible with the sulfopolyester.
- a further general description of miscible and immiscible polymer blends and the various analytical techniques for their characterization may be found in Polymer Blends Volumes 1 and 2, Edited by D.R. Paul and CB. Bucknall, 2000, John Wiley & Sons, Inc.
- Non-limiting examples of water-dispersible polymers that may be blended with the sulfopolyester are polymethacrylic acid, polyvinyl pyrrolidone, polyethylene- acrylic acid copolymers, polyvinyl methyl ether, polyvinyl alcohol, polyethylene oxide, hydroxy propyl cellulose, hydroxypropyl methyl cellulose, methyl cellulose, ethyl hydroxyethyl cellulose, isopropyl cellulose, methyl ether starch, polyacrylamides, poly(N-vinyl caprolactam), polyethyl oxazoline, poly(2-isopropyl-2- oxazoline), polyvinyl methyl oxazolidone, water-dispersible sulfopolyesters, polyvinyl methyl oxazolidimone, poly(2,4-dimethyl-6-triazinylethylene), and ethylene oxide-propylene oxide copolymers.
- blends of more than one sulfopolyester may be used to tailor the end-use properties of the resulting nonwoven fabric or web.
- the blends of one or more sulfopolyesters will have glass transition temperatures of at least 25 0 C. Thus, blending may also be exploited to alter the processing characteristics of a sulfopolyester to facilitate the fabrication of the nonwoven fabric.
- the sulfopolyester and supplemental polymer may be blended in batch, semicontinuous, or continuous processes. Small scale batches may be readily prepared in any high-intensity mixing devices well-known to those skilled in the art, such as Banbury mixers, prior to melt-spinning fibers.
- the components may also be blended in solution in an appropriate solvent.
- the melt blending method includes blending the sulfopolyester and supplemental polymer at a temperature sufficient to melt the polymers.
- the blend may be cooled and pelletized for further use or the melt blend can be melt spun directly from this molten blend into fiber form.
- melt as used herein includes, but is not limited to, merely softening the polyester.
- melt mixing methods generally known in the polymers art, see Mixing and Compounding of Polymers (I. Manas-Zloczower & Z. Tadmor editors, Carl Hanser Verlag Publisher, 1994, New York, N. Y.).
- the sulfopolyester in the multicomponent fiber has a glass transition temperature (Tg) of at least 25 0 C, and the sulfopolyester comprises: (A) about 50 to about 96 mole% of one or more residues of isophthalic acid or terephthalic acid, based on the total acid residues;
- n is an integer in the range of 2 to about 500; (iv) 0 to about 20 mole%, based on the total repeating units, of residues of a branching monomer having 3 or more functional groups wherein the functional groups are hydroxyl, carboxyl, or a combination thereof.
- the multicomponent fiber may optionally include a first water-dispersible polymer blended with the sulfopolyester; and, optionally, a water non-dispersible polymer blended with the sulfopolyester such that the blend is an immiscible blend.
- the first water-dispersible polymer is as described hereinabove.
- the sulfopolyester can have a glass transition temperature (Tg) of at least 25 0 C, but may have, for example, a Tg of about 35 0 C, about 48 0 C, about 55 0 C, about 65 0 C, about 7O 0 C, about 75 0 C, about 85 0 C, and about 9O 0 C.
- the sulfopolyester may contain other concentrations of isophthalic acid residues, for example, about 60 to about 95 mole%, and about 75 to about 95 mole%. Further examples of isophthalic acid residue concentrations ranges are about 70 to about 85 mole%, about 85 to about 95 mole% and about 90 to about 95 mole%.
- the sulfopolyester also may comprise about 25 to about 95 mole% of the residues of diethylene glycol. Further examples of diethylene glycol residue concentration ranges include about 50 to about 95 mole%, about 70 to about 95 mole%, and about 75 to about 95 mole%.
- the sulfopolyester also may include the residues of ethylene glycol and/or 1,4-cyclohexanedimethanol, abbreviated herein as "CFIDM".
- CFIDM 1,4-cyclohexanedimethanol
- Typical concentration ranges of CHDM residues are about 10 to about 75 mole%, about 25 to about 65 mole%, and about 40 to about 60 mole%.
- Typical concentration ranges of ethylene glycol residues are about 10 to about 75 mole%, about 25 to about 65 mole%, and about 40 to about 60 mole%.
- the sulfopolyester comprises about 75 to about 96 mole% of the residues of isophthalic acid and about 25 to about 95 mole% of the residues of diethylene glycol.
- the sulfopolyesters of the instant invention are readily prepared from the appropriate dicarboxylic acids, esters, anhydrides, or salts, sulfomonomer, and the appropriate diol or diol mixtures using typical polycondensation reaction conditions. They may be made by continuous, semi-continuous, and batch modes of operation and may utilize a variety of reactor types. Examples of suitable reactor types include, but are not limited to, stirred tank, continuous stirred tank, slurry, tubular, wiped-film, falling film, or extrusion reactors.
- continuous as used herein means a process wherein reactants are introduced and products withdrawn simultaneously in an uninterrupted manner.
- continuous it is meant that the process is substantially or completely continuous in operation and is to be contrasted with a “batch” process.
- Continuous is not meant in any way to prohibit normal interruptions in the continuity of the process due to, for example, start-up, reactor maintenance, or scheduled shut down periods.
- batch process as used herein means a process wherein all the reactants are added to the reactor and then processed according to a predetermined course of reaction during which no material is fed or removed into the reactor.
- continuous means a process where some of the reactants are charged at the beginning of the process and the remaining reactants are fed continuously as the reaction progresses.
- a semicontinuous process may also include a process similar to a batch process in which all the reactants are added at the beginning of the process except that one or more of the products are removed continuously as the reaction progresses.
- the process is operated advantageously as a continuous process for economic reasons and to produce superior coloration of the polymer as the sulfopolyester may deteriorate in appearance if allowed to reside in a reactor at an elevated temperature for too long a duration.
- the sulfopolyesters of the present invention are prepared by procedures known to persons skilled in the art. The sulfomonomer is most often added directly to the reaction mixture from which the polymer is made, although other processes are known and may also be employed, for example, as described in U. S. Patent No.'s -3,018,272, 3,075,952, and 3,033,822.
- the reaction of the sulfomonomer, diol component and the dicarboxylic acid component may be carried out using conventional polyester polymerization conditions.
- the reaction process may comprise two steps.
- the diol component and the dicarboxylic acid component such as, for example, dimethyl isophthalate
- the reaction process may comprise two steps.
- the diol component and the dicarboxylic acid component such as, for example, dimethyl isophthalate
- the diol component and the dicarboxylic acid component are reacted at elevated temperatures, typically, about 15O 0 C to about 25O 0 C for about 0.5 to about 8 hours at pressures ranging from about 0.0 kPa gauge to about 414 kPa gauge (60 pounds per square inch, "psig").
- the temperature for the ester interchange reaction ranges from about 18O 0 C to about 23O 0 C for about 1 to about 4 hours while the preferred pressure ranges from about 103 kPa gauge (15 psig) to about 276 kPa gauge (40 psig).
- reaction product is heated under higher temperatures and under reduced pressure to form sulfopolyester with the elimination of diol, which is readily volatilized under these conditions and removed from the system.
- This second step, or polycondensation step is continued under higher vacuum and a temperature which generally ranges from about 23O 0 C. to about 35O 0 C, preferably about 25O 0 C to about 31O 0 C and most preferably about 26O 0 C to about 29O 0 C for about 0.1 to about 6 hours, or preferably, for about 0.2 to about 2 hours, until a polymer having the desired degree of polymerization, as determined by inherent viscosity, is obtained.
- the polycondensation step may be conducted under reduced pressure which ranges from about 53 kPa (400 torr) to about 0.013 kPa (0.1 torr). Stirring or appropriate conditions are used in both stages to ensure adequate heat transfer and surface renewal of the reaction mixture.
- the reactions of both stages are facilitated by appropriate catalysts such as, for example, alkoxy titanium compounds, alkali metal hydroxides and alcoholates, salts of organic carboxylic acids, alkyl tin compounds, metal oxides, and the like.
- a three-stage manufacturing procedure similar to that described in U.S. Patent No. 5,290,631, may also be used, particularly when a mixed monomer feed of acids and esters is employed.
- sulfopolyesters are produced by reacting the dicarboxylic acid or a mixture of dicarboxylic acids with the diol component or a mixture of diol components.
- the reaction is conducted at a pressure of from about 7 kPa gauge (1 psig) to about 1379 kPa gauge (200 psig), preferably less than 689 kPa (100 psig) to produce a low molecular weight, linear or branched sulfopolyester product having an average degree of polymerization of from about 1.4 to about 10.
- the temperatures employed during the direct esterification reaction typically range from about 18O 0 C to about 28O 0 C. Another range is from about 22O 0 C to about 27O 0 C. This low molecular weight polymer may then be polymerized by a polycondensation reaction.
- the multicomponent fibers, nonwoven fabrics, and fibrous articles of this invention also may contain other conventional additives and ingredients which do not deleteriously affect their end use.
- additives such as fillers, surface friction modifiers, light and heat stabilizers, extrusion aids, antistatic agents, colorants, dyes, pigments, fluorescent brighteners, antimicrobials, anticounterfeiting markers, hydrophobic and hydrophilic enhancers, viscosity modifiers, slip agents, tougheners, adhesion promoters, and the like may be used.
- the multicomponent fibers, nonwoven fabrics, and fibrous articles of our invention do not require the presence of additives such as, for example, pigments, fillers, oils, waxes, or fatty acid finishes, to prevent blocking or fusing of the fibers during processing.
- additives such as, for example, pigments, fillers, oils, waxes, or fatty acid finishes
- blocking or fusing is understood to mean that the fibers or fibrous articles stick together or fuse into a mass such that the fiber cannot be processed or used for its intended purpose. Blocking and fusing can occur during processing of the fiber or fibrous article or during storage over a period of days or weeks and is exacerbated under hot, humid conditions.
- the multicomponent fibers, nonwoven fabrics, and fibrous articles can contain less than 10 wt% of such anti-blocking additives, based on the total weight of the multicomponent fiber or fibrous article.
- the multicomponent fibers and fibrous articles may contain less than 10 wt% of a pigment or filler.
- the multicomponent fibers, nonwoven fabrics, and fibrous articles may contain less than 9 wt%, less than 5 wt%, less than 3 wt%, less than 1 wt%, and 0 wt% of a pigment or filler, based on the total weight of the multicomponent fiber.
- Colorants sometimes referred to as toners, may be added to impart a desired neutral hue and/or brightness to the sulfopolyester.
- pigments or colorants may be included in the sulfopolyester reaction mixture during the reaction of the diol monomer and the dicarboxylic acid monomer or they may be melt blended with the preformed sulfopolyester.
- a preferred method of including colorants is to use a colorant having thermally stable organic colored compounds having reactive groups such that the colorant is copolymerized and incorporated into the sulfopolyester to improve its hue.
- colorants such as dyes possessing reactive hydroxyl and/or carboxyl groups, including, but not limited to, blue and red substituted anthraquinones, may be copolymerized into the polymer chain.
- dyes may be added to the copolyester reaction process after an ester interchange or direct esterification reaction.
- the sulfopolyesters contained in the multicomponent fiber has a glass transition temperature (Tg) of at least 57 0 C.
- a glass transition temperature (Tg) of at least 57 0 C has been found to particularly useful for multicomponent fibers to prevent blocking and fusing of the multicomponent fiber during spinning and take up.
- a multicomponent fiber having shaped cross section is utilized to produce the nonwoven fabric comprising: (A) a water dispersible sulfopolyester having a glass transition temperature (Tg) of at least 57 0 C, the sulfopolyester comprising:
- residues of one or more dicarboxylic acids (i) residues of one or more dicarboxylic acids; (ii) about 4 to about 40 mole%, based on the total repeating units, of residues of at least one sulfomonomer having 2 functional groups and one or more sulfonate groups attached to an aromatic or cycloaliphatic ring wherein the functional groups are hydroxyl, carboxyl, or a combination thereof;
- n is an integer in the range of 2 to about 500;
- the dicarboxylic acids, diols, sulfopolyester, sulfomonomers, and branching monomers residues are as described previously for other embodiments of the invention.
- the sulfopolyester have a Tg of at least 57 0 C.
- Further examples of glass transition temperatures that may be exhibited by the sulfopolyester or sulfopolyester blend of the multicomponent fiber are at least 6O 0 C, at least 65 0 C, at least 70 0 C, at least 75 0 C, at least 8O 0 C, at least 85 0 C, and at least 9O 0 C.
- blends of one or more sulfopolyesters may be used in varying proportions to obtain a sulfopolyester blend having the desired Tg.
- the Tg of a sulfopolyester blend may be calculated by using a weighted average of the glass transition temperatures of the sulfopolyester components.
- sulfopolyester having a Tg of 48 0 C may be blended in a 25:75 wt:wt ratio with another sulfopolyester having Tg of 65 0 C to give a sulfopolyester blend having a Tg of approximately 61 0 C.
- the water dispersible sulfopolyester component of the multicomponent fiber presents properties which allow at least one of the following:
- a multicomponent fiber is utilized having a shaped cross section comprising: (A) at least one water dispersible sulfopolyester; and
- the sulfopolyester utilized in these multicomponent fibers has a melt viscosity of generally less than about 12,000 poise. Other ranges of melt viscosity of the sulfopolyester is less than 10,000 poise, less than 6,000, and less than 4,000 poise measured at 240°C and 1 rad/sec shear rate. In another aspect, the sulfopolyester exhibits a melt viscosity ranging from about 1000 to about 12000 poise, from about 2000 to about 6000 poise,, or from about 2500 to about 4000 poise measured at 240°C and 1 rad/sec shear rate. Prior to determining the viscosity, the samples are dried at 60°C in a vacuum oven for 2 days.
- the melt viscosity is measured using a rheometer having a 25 mm diameter parallel-plate geometry at lmm gap setting. A dynamic frequency sweep is run at a strain rate range of 1 to 400 rad/sec and 10% strain amplitude. The viscosity is then measured at 24O 0 C and strain rate of 1 rad/sec.
- the level of sulfomonomer residues in the sulfopolyester polymers for use in this embodiment of the invention is generally less than about 25 mole % or less than 20 mole %, reported as a percentage of the total diacid or diol residues in the sulfopolyester.
- the level of sulfomonomer residues in the sulfopolyester polymers range from about 4 to about 20 mole %, about 5 to about 12 mole %, and between about 7 to about 10 mole %.
- the sulfomonomers for use with the invention can have 2 functional groups and one or more sulfonate groups attached to an aromatic or cycloaliphatic ring wherein the functional groups are hydroxyl, carboxyl, or a combination thereof, for example, sodiosulfo-isophthalic acid monomer.
- the sulfopolyester can comprise residues of one or more dicarboxylic acids, one or more diol residues wherein at least 25 mole %, based on the total diol residues, is a poly(ethylene glycol) having a structure H-(OCH 2 -CH 2 ) n -OH wherein n is an integer in the range of 2 to about 500, and 0 to about 20 mole %, based on the total repeating units, of residues of a branching monomer having 3 or more functional groups wherein the functional groups are hydroxyl, carboxyl, or a combination thereof.
- the sulfopolyester comprises from about
- the dicarboxylic portion of the sulfopolyester comprises between about 60-80 mole % terephthalic acid, about 0-30 mole % isophthalic acid, and about 4-20 mole % 5- sodiosulfoisophthalic acid (5-SSIPA).
- the diol portion comprises from about 0-50 mole % diethylene glycol and from about 50-100 mole % ethylene glycol.
- the water non-dispersible component of the multicomponent fiber may comprise any of those water non-dispersible polymers described herein. Spinning of the multicomponent fiber may also occur according to any method described herein. However, the improved rheological properties of multicomponent fibers in accordance with this aspect of the invention provide for enhanced drawings speeds.
- the water dispersible sulfopolyester has a melt viscosity of less than about 12,000 poise measured at 240°C at a strain rate of 1 rad/sec, and wherein the sulfopolyester comprises less than about 25 mole % of residues of at least one sulfomonomer, based on the total moles of diacid or diol residues, and is extruded to produce multicomponent extrudates
- the multicomponent extrudate is capable of being melt drawn to produce the multicomponent fiber, using any of the methods disclosed herein, at a speed of at least about 2000 m/min.
- the multicomponent extrudate is capable of being melt drawn at a speed in the following ranges: at least about 3000 m/min, at least about 4000 m/min, or at least about 4500 m/min.
- melt drawing of the multicomponent extrudates at these speeds results in at least some oriented crystallinity in the water non-dispersible component of the multicomponent fiber. This oriented crystallinity can increase the dimensional stability of nonwoven fabrics made from the multicomponent fibers during subsequent processing.
- Another advantage of the multicomponent extrudate produced from sulfopolyesters having a melt viscosity of less than about 12,000 poise measured at 240°C at a strain rate of 1 rad/sec, and wherein the sulfopolyester comprises less than about 25 mole % of residues of at least one sulfomonomer, based on the total moles of diacid or diol residues, is that it can be melt drawn to a multicomponent fiber having an as-spun denier of less than 6 deniers per filament.
- Other ranges of multicomponent fiber sizes include an as-spun denier of less than 4 deniers per filament and less than 2.5 deniers per filament.
- the multicomponent fiber comprises a plurality of segments or domains of one or more water non-dispersible polymers immiscible with the sulfopolyester in which the segments or domains are substantially isolated from each other by the sulfopolyester intervening between the segments or domains.
- substantially isolated is intended to mean that the segments or domains are set apart from each other to permit the segments domains to form individual fibers upon removal of the sulfopolyester.
- the segments or domains may be touching each others as in, for example, a segmented pie configuration but can be split apart by impact or when the sulfopolyester is removed.
- the ratio by weight of the sulfopolyester to water non-dispersible polymer component in the multicomponent fiber of the invention is generally in the range of about 60:40 to about 2:98 or, in another example, in the range of about 50:50 to about 5:95.
- the sulfopolyester comprises 50% by weight or less of the total weight of the multicomponent fiber.
- the segments or domains of the multicomponent fiber comprise one of more water non-dispersible polymers.
- water non-dispersible polymers which are used in segments of the multicomponent fiber include, but are not limited to, polyolefins, polyesters, polyamides, polylactides, polycaprolactone, polycarbonate, polyurethane, and polyvinyl chloride.
- the water non-dispersible polymer may be polyester such as poly(ethylene) terephthalate, poly(butylene) terephthalate, poly(cyclohexylene) cyclohexanedicarboxylate, poly(cyclohexylene) terephthalate, poly(trimethylene) terephthalate, and the like.
- the water non-dispersible polymer is poly(ethylene) terephthalate having an inherent viscosity of less than 0.6 dL/g, measured in a 60/40 parts by weight solution of phenol/tetrachloroethane solvent at 25 0 C and at a concentration of about 0.5 g of poly(ethylene) terephthalate in 100 mL of solvent. Other ranges are less than 0.55 dL/g, less than 0.4_dL/g, and less than 0.3 dL/g. PET having this inherent viscosity can produce improved nonwoven fabrics having good fiber entanglement and less loose fibers on the surface of the nonwoven fabric.
- the water non-dispersible polymer can be biodistintegratable as determined by DIN Standard 54900 and/or biodegradable as determined by ASTM Standard Method, D6340-98.
- biodegradable polyesters and polyester blends are disclosed in U.S. Patent No.'s 5,599,858;
- biodegradable as used herein in reference to the water non-dispersible polymers of the present invention, is understood to mean that the polymers are degraded under environmental influences such as, for example, in a composting environment, in an appropriate and demonstrable time span as defined, for example, by ASTM Standard Method, D6340- 98, entitled “Standard Test Methods for Determining Aerobic Biodegradation of Radiolabeled Plastic Materials in an Aqueous or Compost Environment".
- the water non-dispersible polymers of the present invention also may be "biodisintegratable", meaning that the polymers are easily fragmented in a composting environment as defined, for example, by DIN Standard 54900.
- the biodegradable polymer is initially reduced in molecular weight in the environment by the action of heat, water, air, microbes and other factors. This reduction in molecular weight results in a loss of physical properties (tenacity) and often in fiber breakage.
- the monomers and oligomers are then assimilated by the microbes. In an aerobic environment, these monomers or oligomers are ultimately oxidized to CO 2 , H 2 O, and new cell biomass. In an anaerobic environment, the monomers or oligomers are ultimately converted to CO 2 , H 2 , acetate, methane, and cell biomass.
- water non-dispersible polymer may be an aliphatic-aromatic polyester, abbreviated herein as "AAPE".
- aliphatic-aromatic polyester means a polyester comprising a mixture of residues from aliphatic or cycloaliphatic dicarboxylic acids or diols and aromatic dicarboxylic acids or diols.
- non-aromatic as used herein with respect to the dicarboxylic acid and diol monomers of the present invention, means that carboxyl or hydroxyl groups of the monomer are not connected through an aromatic nucleus.
- adipic acid contains no aromatic nucleus in its backbone, i.e., the chain of carbon atoms connecting the carboxylic acid groups, thus is “non-aromatic".
- aromatic means the dicarboxylic acid or diol contains an aromatic nucleus in the backbone such as, for example, terephthalic acid or 2,6-naphthalene dicarboxylic acid.
- Non-aromatic is intended to include both aliphatic and cycloaliphatic structures such as, for example, diols and dicarboxylic acids, which contain as a backbone a straight or branched chain or cyclic arrangement of the constituent carbon atoms which may be saturated or paraffinic in nature, unsaturated, i.e., containing non-aromatic carbon-carbon double bonds, or acetylenic, i.e., containing carbon- carbon triple bonds.
- diols and dicarboxylic acids which contain as a backbone a straight or branched chain or cyclic arrangement of the constituent carbon atoms which may be saturated or paraffinic in nature, unsaturated, i.e., containing non-aromatic carbon-carbon double bonds, or acetylenic, i.e., containing carbon- carbon triple bonds.
- non-aromatic is intended to include linear and branched, chain structures (referred to herein as “aliphatic”) and cyclic structures (referred to herein as “alicyclic” or “cycloaliphatic”).
- aliphatic chain structures
- cyclic cycloaliphatic
- the difunctional carboxylic acid typically is a aliphatic dicarboxylic acid such as, for example, adipic acid, or an aromatic dicarboxylic acid such as, for example, terephthalic acid.
- the difunctional hydroxyl compound may be cycloaliphatic diol such as, for example, 1 ,4-cyclohexanedimethanol, a linear or branched aliphatic diol such as, for example, 1,4-butanediol, or an aromatic diol such as, for example, hydroquinone.
- cycloaliphatic diol such as, for example, 1 ,4-cyclohexanedimethanol
- a linear or branched aliphatic diol such as, for example, 1,4-butanediol
- an aromatic diol such as, for example, hydroquinone.
- the AAPE may be a linear or branched random copolyester and/or chain extended copolyester comprising diol residues which comprise the residues of one or more substituted or unsubstituted, linear or branched, diols selected from aliphatic diols containing 2 to about 8 carbon atoms, polyalkylene ether glycols containing 2 to 8 carbon atoms, and cycloaliphatic diols containing about 4 to about 12 carbon atoms.
- the substituted diols typically, will comprise 1 to about 4 substituents independently selected from halo, C 6 -C 10 aryl, and Ci-C 4 alkoxy.
- diols which may be used include, but are not limited to, ethylene glycol, diethylene glycol, propylene glycol, 1 ,3-propanediol, 2,2-dimethyl-l,3-propanediol, 1,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, polyethylene glycol, diethylene glycol, 2,2,4- trimethyl-l,6-hexanediol, thiodiethanol, 1,3-cyclohexanedimethanol, 1,4-cyclo- hexanedimethanol, 2,2,4,4-tetramethyl-l,3-cyclobutanediol, triethylene glycol, and tetraethylene glycol with the preferred diols comprising one or more diols selected from 1,4-butanediol; 1,3-propanediol; ethylene glycol
- the AAPE also comprises diacid residues which contain about 35 to about 99 mole%, based on the total moles of diacid residues, of the residues of one or more substituted or unsubstituted, linear or branched, non-aromatic dicarboxylic acids selected from aliphatic dicarboxylic acids containing 2 to about 12 carbon atoms and cycloaliphatic acids containing about 5 to about 10 carbon atoms.
- the substituted non-aromatic dicarboxylic acids will typically contain 1 to about 4 substituents selected from halo, C 6 -C 10 aryl, and CpC 4 alkoxy.
- Non-limiting examples of non-aromatic diacids include malonic, succinic, glutaric, adipic, pimelic, azelaic, sebacic, fumaric, 2,2-dimethyl glutaric, suberic, 1,3- cyclopentanedicarboxylic, 1 ,4-cyclohexanedicarboxylic, 1,3- cyclohexanedicarboxylic, diglycolic, itaconic, maleic, and 2,5-norbornane- dicarboxylic.
- the AAPE comprises about 1 to about 65 mole%, based on the total moles of diacid residues, of the residues of one or more substituted or unsubstituted aromatic dicarboxylic acids containing 6 to about 10 carbon atoms.
- substituted aromatic dicarboxylic acids they will typically contain 1 to about 4 substituents selected from halo, C 6 -Ci 0 aryl, and CpC 4 alkoxy.
- Non-limiting examples of aromatic dicarboxylic acids which may be used in the AAPE of our invention are terephthalic acid, isophthalic acid, salts of 5-sulfoisophthalic acid, and 2,6- naphthalenedicarboxylic acid. More preferably, the non-aromatic dicarboxylic acid will comprise adipic acid, the aromatic dicarboxylic acid will comprise terephthalic acid, and the diol will comprise 1 ,4-butanediol.
- compositions for the AAPE 's of our invention are those prepared from the following diols and dicarboxylic acids (or polyester-forming equivalents thereof such as diesters) in the following mole percentages, based on 100 mole percent of a diacid component and 100 mole percent of a diol component:
- glutaric acid about 30 to about 75%); terephthalic acid (about 25 to about 70%); 1,4-butanediol (about 90 to 100%); and modifying diol (0 about 10%);
- succinic acid about 30 to about 95%
- terephthalic acid about 5 to about 70%
- 1 ,4-butanediol about 90 to 100%
- modifying diol (0 to about 10%)
- adipic acid about 30 to about 75%); terephthalic acid (about 25 to about 70%); 1,4-butanediol (about 90 to 100%); and modifying diol (0 to about 10%).
- the modifying diol preferably is selected from 1 ,4-cyclohexanedimethanol, triethylene glycol, polyethylene glycol and neopentyl glycol.
- the most preferred AAPE's are linear, branched or chain extended copolyesters comprising about 50 to about 60 mole percent adipic acid residues, about 40 to about 50 mole percent terephthalic acid residues, and at least 95 mole percent 1 ,4-butanediol residues.
- the adipic acid residues comprise about 55 to about 60 mole percent
- the terephthalic acid residues comprise about 40 to about 45 mole percent
- the diol residues comprise about 95 mole percent 1 ,4-butanediol residues.
- Such compositions are commercially available under the trademark EASTAR BIO ® copolyester from Eastman Chemical Company, Kingsport, TN, and under the trademark ECOFLEX ® from BASF Corporation.
- AAPE's include a poly(tetra- methylene glutarate-co-terephthalate) containing (a) 50 mole percent glutaric acid residues, 50 mole percent terephthalic acid residues, and 100 mole percent 1,4- butanediol residues, (b) 60 mole percent glutaric acid residues, 40 mole percent terephthalic acid residues, andlOO mole percent 1,4-butanediol residues or (c) 40 mole percent glutaric acid residues, 60 mole percent terephthalic acid residues, and 100 mole percent 1 ,4-butanediol residues; a poly(tetramethylene succinate-co- terephthalate) containing (a) 85 mole percent succinic acid residues, 15 mole percent terephthalic acid residues, and 100 mole percent 1 ,4-butanediol residues or (b) 70 mole percent succinic acid residue
- the AAPE preferably comprises from about 10 to about 1,000 repeating units and preferably, from about 15 to about 600 repeating units.
- the AAPE may have an inherent viscosity of about 0.4 to about 2.0 dL/g, or more preferably about 0.7 to about 1.6 dL/g, as measured at a temperature of 25 0 C using a concentration of 0.5 gram copolyester in 100 ml of a 60/40 by weight solution of phenol/tetrachloroethane.
- the AAPE may contain the residues of a branching agent.
- the mole percentage ranges for the branching agent are from about 0 to about 2 mole%, preferably about 0.1 to about 1 mole%, and most preferably about 0.1 to about 0.5 mole% based on the total moles of diacid or diol residues (depending on whether the branching agent contains carboxyl or hydroxyl groups).
- the branching agent preferably has a weight average molecular weight of about 50 to about 5000, more preferably about 92 to about 3000, and a functionality of about 3 to about 6.
- the branching agent may be the esterif ⁇ ed residue of a polyol having 3 to 6 hydroxyl groups, a polycarboxylic acid having 3 or 4 carboxyl groups (or ester- forming equivalent groups ) or a hydroxy acid having a total of 3 to 6 hydroxyl and carboxyl groups.
- the AAPE may be branched by the addition of a peroxide during reactive extrusion.
- Each segment of the water non-dispersible polymer may be different from others in fineness and may be arranged in any shaped or engineered cross-sectional geometry known to persons skilled in the art.
- the sulfopolyester and a water non-dispersible polymer may be used to prepare a multicomponent fiber having an engineered geometry such as, for example, a side-by-side, "islands-in-the-sea", segmented pie, other splitables, sheath/core, or other configurations known to persons skilled in the art.
- Other multicomponent configurations are also possible. Subsequent removal of a side, the "sea", or a portion of the "pie” can result in very fine fibers.
- the process of preparing multicomponent fibers also is well known to persons skilled in the art.
- the sulfopolyester fibers of this invention may be present in amounts of about 10 to about 90 weight% and will generally be used in the sheath portion of sheath/core fibers.
- the other component may be from a wide range of other polymeric materials such as, for example, poly(ethylene) terephthalate, poly(butylene) terephthalate, poly(trimethylene) terephthalate, polylactides and the like as well as polyolefins, cellulose esters, and polyamides.
- the resulting bicomponent or multicomponent fiber is not completely water-dispersible.
- Side by side combinations with significant differences in thermal shrinkage can be utilized for the development of a spiral crimp. If crimping is desired, a saw tooth or stuffer box crimp is generally suitable for many applications. If the second polymer component is in the core of a sheath/core configuration, such a core optionally may be stabilized.
- the sulfopolyesters are particularly useful for fibers having an "islands-in-the- sea” or “segmented pie” cross section as they only requires neutral or slightly acidic (i.e., "soft” water) to disperse, as compared to the caustic-containing solutions that are sometimes required to remove other water dispersible polymers from multicomponent fibers.
- the multicomponent fiber comprises: (A) a water dispersible sulfopolyester having a glass transition temperature (Tg) of at least 57 0 C, the sulfopolyester comprising:
- n is an integer in the range of 2 to about 500; (iv) 0 to about 20 mole%, based on the total repeating units, of residues of a branching monomer having 3 or more functional groups wherein the functional groups are hydroxyl, carboxyl, or a combination thereof; and (B) a plurality of segments comprising one or more water non-dispersible polymers immiscible with the sulfopolyester, wherein the segments are substantially isolated from each other by the sulfopolyester intervening between the segments; wherein the fiber has an islands-in-the-sea or segmented pie cross section.
- the dicarboxylic acids, diols, sulfopolyester, sulfomonomers, branching monomers residues, and water non-dispersible polymers are as described previously.
- sulfopolyester have a Tg of at least 57 0 C.
- the sulfopolyester may be a single sulfopolyester or a blend of one or more sulfopolyester polymers.
- glass transition temperatures that may be exhibited by the sulfopolyester or sulfopolyester blends are at least 65 0 C, at least 7O 0 C, at least 75 0 C, at least 85 0 C, and at least 9O 0 C.
- the sulfopolyester may comprise about 75 to about 96 mole% of one or more residues of isophthalic acid or terephthalic acid and about 25 to about 95 mole% of a residue of diethylene glycol.
- examples of the water non-dispersible polymers are polyolefins, polyesters, polyamides, polylactides, polycaprolactone, polycarbonate, polyurethane, and polyvinyl chloride.
- the water non-dispersible polymer may be biodegradable or biodisintegratable.
- the water non-dispersible polymer may be an aliphatic-aromatic polyester as described previously.
- the multicomponent fiber may be prepared by any number of methods known to persons skilled in the art.
- the multicomponent fiber having a shaped cross section is produced by a process comprising: spinning a water dispersible sulfopolyester having a glass transition temperature (Tg) of at least 57 0 C and one or more water non-dispersible polymers immiscible with the sulfopolyester into a fiber, the sulfopolyester comprising: (i) residues of one or more dicarboxylic acids; (ii) about 4 to about 40 mole%, based on the total repeating units, of residues of at least one sulfomonomer having 2 functional groups and one or more sulfonate groups attached to an aromatic or cycloaliphatic ring wherein the functional groups are hydroxyl, carboxyl, or a combination thereof;
- n is an integer in the range of 2 to about 500;
- the multicomponent fiber may be prepared by melting the sulfopolyester and one or more water non-dispersible polymers in separate extruders and directing the individual polymer flows into one spinneret or extrusion die with a plurality of distribution flow paths such that the water non-dispersible polymer component form small segments or thin strands which are substantially isolated from each other by the intervening sulfopolyester.
- the cross section of such a fiber may be, for example, a segmented pie arrangement or an islands-in-the-sea arrangement.
- the sulfopolyester and one or more water non-dispersible polymers are separately fed to the spinneret orifices and then extruded in sheath-core form in which the water non-dispersible polymer forms a "core" that is substantially enclosed by the sulfopolyester "sheath" polymer.
- the orifice supplying the "core" polymer is in the center of the spinning orifice outlet and flow conditions of core polymer fluid are strictly controlled to maintain the concentricity of both components when spinning. Modifications in spinneret orifices enable different shapes of core and/or sheath to be obtained within the fiber cross- section.
- a multicomponent fiber having a side-by-side cross section or configuration may be produced by coextruding the water dispersible sulfopolyester and water non-dispersible polymer through orifices separately and converging the separate polymer streams at substantially the same speed to merge side-by-side as a combined stream below the face of the spinneret; or (2) by feeding the two polymer streams separately through orifices, which converge at the surface of the spinneret, at substantially the same speed to merge side-by-side as a combined stream at the surface of the spinneret.
- the velocity of each polymer stream, at the point of merge is determined by its metering pump speed, the number of orifices, and the size of the orifice.
- the dicarboxylic acids, diols, sulfopolyester, sulfomonomers, branching monomers residues, and water non-dispersible polymers are as described previously.
- the sulfopolyester has a glass transition temperature of at least 57 0 C. Further examples of glass transition temperatures that may be exhibited by the sulfopolyester or sulfopolyester blend are at least 65 0 C, at least 7O 0 C, at least 75 0 C, at least 85 0 C, and at least 9O 0 C.
- the sulfopolyester may comprise about 50 to about 96 mole% of one or more residues of isophthalic acid or terephthalic acid, based on the total acid residues; and about 4 to about 30 mole%, based on the total acid residues, of a residue of sodiosulfoisophthalic acid; and 0 to about 20 mole%, based on the total repeating units, of residues of a branching monomer having 3 or more functional groups wherein the functional groups are hydroxyl, carboxyl, or a combination thereof.
- the sulfopolyester may comprise about 75 to about 96 mole% of one or more residues of isophthalic acid or terephthalic acid and about 25 to about 95 mole% of a residue of diethylene glycol.
- examples of the water non-dispersible polymers are polyolefins, polyesters, polyamides, polylactides, polycaprolactone, polycarbonate, polyurethane, and polyvinyl chloride.
- the water non-dispersible polymer may be biodegradable or biodisintegratable.
- the water non-dispersible polymer may be an aliphatic-aromatic polyester as described previously. Examples of shaped cross sections include, but are not limited to, islands-in-the-sea, side-by-side, sheath- core, or segmented pie configurations.
- the multicomponent fiber having a shaped cross section is produced by a process comprising: spinning at least one water dispersible sulfopolyester and one or more water non-dispersible polymers immiscible with the sulfopolyester to produce a multicomponent fiber, wherein the multicomponent fiber has a plurality of domains comprising the water non-dispersible polymers and the domains are substantially isolated from each other by the sulfopolyester intervening between the domains; wherein the water dispersible sulfopolyester exhibits a melt viscosity of less than about 12,000 poise measured at 240°C at a strain rate of 1 rad/sec, and wherein the sulfopolyester comprising less than about 25 mole % of residues of at least one sulfomonomer, based on the total moles of diacid or diol residues; and wherein the multicomponent fiber has an as- spun denier of less
- the multicomponent fiber having a shaped cross section can be produced by a process comprising: (A) extruding at least one water dispersible sulfopolyester and one or more water non-dispersible polymers immiscible with said sulfopolyester to produce a multicomponent extrudate, wherein the multicomponent extrudate has a plurality of domains comprising the water non-dispersible polymers and the domains are substantially isolated from each other by the sulfopolyester intervening between the domains; and (B) melt drawing the multicomponent extrudate at a speed of at least about 2000 m/min to produce the multicomponent fiber.
- the process includes the step of melt drawing the multicomponent extrudate at a speed of at least about 2000 m/min, more preferably, at least about 3000 m/min, and most preferably at least 4500 m/min.
- the fibers are quenched with a cross flow of air whereupon the fibers solidify.
- Various finishes and sizes may be applied to the fiber at this stage.
- the cooled fibers typically, are subsequently drawn and wound up on a take up spool.
- Other additives may be incorporated in the finish in effective amounts like emulsifiers, antistatics, antimicrobials, antifoams, lubricants, thermostabilizers, UV stabilizers, and the like.
- the drawn fibers may be textured and wound-up to form a bulky continuous filament.
- This one-step technique is known in the art as spin-draw- texturing.
- Other embodiments include flat filament (non-textured) yarns, or cut staple fiber, either crimped or uncrimped.
- Step (A) of the inventive process comprises collecting the multicomponent fibers to form a non- woven web.
- the multicomponents fibers produced by the processes discussed previously can be collected in a manner to produce a nonwoven web such that a support for the multicomponent fibers is not necessary. This can be accomplished by any method known in the art.
- the multicomponent fibers can be subjected to such processes as mechanical needling, chemical binding, thermally calendaring, ultrasonic fusing, or hydroentangling, in order to provide enough consolidation where a support for the multicomponent fibers is not necessary.
- mechanical needling is needle punching.
- the amount of hydroentangling energy expended in this process can range from about 20% to about 50% of the hydroentangling energy expended in Step (C) of the process.
- hydroentangling after sulfopolyester removal, (Step C) of the process is the step where the majority of the energy is expended to interlock the multicomponent fibers to produce the nonwoven fabric.
- extrusion technology can be utilized to produce the nonwoven web of Step (A) from the materials used to make the multicomponent fibers themselves, thus eliminating the multicomponent fiber production step.
- processes include spunbond and meltblown processes.
- the spunbond process tranforms the water dispersible sulfopolyester and water non- dispersible polymer directly into a nonwoven web by extruding multicomponent fibers, orienting them as bundles or groupings, and layering them on a conveying screen, without a separate fiber production step.
- the multicomponent fiber is first spun and collected, then formed into a fabric by a separate process. Therefore, the water dispersible sulfopolyester and water non- dispersible polymer are routed through the spunbond process to yield a nonwoven web of Step (A).
- Figure 1 shows the spunbond process.
- the water dispersible sulfopolyester and water non-dispersible polymer are heated to the liquid state and as it passes through an extrusion orifice, it is injected with sonic velocity air at about 250 to 500°C.
- the fast moving air stream stretches the molten polymer and solidifies it to produce fine multicomponent fibers.
- the multicomponent fibers are then separated from the air stream as an entangled web and compressed between heated rolls to produce the nonwoven web of Step (A).
- the weight of the nonwoven web can range from about 10 grams/m 2 to about 800 grams/m 2 . Other ranges are 10 grams/m 2 to 600 grams/m 2 , 10 grams/m 2 to 400 grams/m 2 , 50 grams/m 2 to 300 grams/m 2 grams/m 2 , and about 50 grams/m 2 to about 150 grams/m 2 .
- Step (B) of the inventive process comprises contacting the nonwoven web with water at a sufficient extraction temperature and pressure to remove a portion of the water dispersible sulfopolyester thereby forming a microfiber web.
- the multicomponent fiber can be contacted with water at an extraction temperature of about 2O 0 C to about 100 0 C.
- Other extraction temperature ranges are from 25 0 C to about 100 0 C and from about 4O 0 C to about 9O 0 C.
- the extraction temperature is defined by the following procedure.
- a nonwoven web consisting of multicomponent fibers with a known water dispersible sulfopolyester content is weighed and then taped to a metal backing plate and covered with a 100 - 200 mesh stainless steel screen on top.
- the backing plate with nonwoven fabric is placed in a deionized water bath at a test temperature in the range about 2O 0 C to about 60°C for 10 minutes to extract the water dispersible sulfopolyester.
- the specimen is removed from the water, and the excess water is removed by placing an absorbent towel above the screen mesh and squeezing.
- the conditioned fabric web is dried in a forced air oven at 60°C and the final weight is measured.
- the weight loss due to extraction is calculated as a percentage of the starting weight.
- the temperature of the conditioning water at which greater than 80% of the sulfopolyester polymer in the starting fiber is removed during the conditioning is designated as the sulfopolyester extraction temperature.
- the temperature, pressure, contact time of the water are such that the water dispersible sulfopolyester is removed, and the nonwoven web remains sufficiently intact as a structure.
- the pressure of the water can range from about 30 barr to about 600 barr. Other pressure ranges are 50 barr to 300 barr.
- the nonwoven web can be contacted with water for a time sufficient to remove about 30% by weight to about 100% by weight of the total water dispersible sulfopolyester contained in the multicomponent fiber. In another embodiment of the invention, greater than 90% by weight of the total water dispersible sulfopolyester is removed from the nonwoven web. In another embodiment, greater than 95% by weight of the total water dispersible sulfopolyester is removed from the nonwoven web.
- the nonwoven web is contacted with water for a time period of from about 10 to about 600 seconds whereby the water dispersible sulfopolyester is dissipated or dissolved.
- the remaining water non-dispersible polymer microfibers can have an average fineness of less than 30% of the denier of the starting multicomponent fiber.
- the remaining water non-dispersible polymer microfibers typically will have an average fineness of 1 d/f or less, typically, 0.5 d/f or less, or more typically, 0.1 d/f or less.
- the nonwoven web is contacted with water via any method known in the art.
- water jets can be utilized.
- one to eight water jet heads can be utilized. The amount of water used ranges from less than 500 times to less than 1000 times the weight of the nonwoven web prior to contacting with water.
- the wash water containing the water-dispersible sulfopolyester can be recycled. In one embodiment of the invention, 80% or more of the wash water is recycled. This is quite an advancement since in conventional processes to produce nonwoven fabrics, the wash water generally cannot be recycled due to the water dispersible sulfopolyester that may plug equipment and may cause excess machine wear. In another embodiment of the invention, substantially all of the sulfopolyester is removed from the wash water. Sulfopolyester recycling processes are described in U.S. Patent Application Serial Number 11/343,955 filed January 31 st , 2006 to Gupta entitled "Sulfopolyester Recovery", which is hereby incorporated by reference to the extent it does not contradict the statements herein.
- Step (C) comprises hydroentangling the microfiber web to produce the nonwoven fabric.
- the water temperature during hydroentangling is less than 40°C.
- the pressure can range from about 150 bar to about 220 bar.
- less than 1% by weight of the water dispersible sulfopolyester is removed from the microfiber web.
- the amount of water dispersible sulfopolyester removed can be less than 0.8% by weight, less than 0.5% by weight, less than 0.25% by weight, less than 0.1% by weight, less than 0.08% by weight, less than 0.05% by weight, and less than 0.02% by weight based on the weight of the microfiber web.
- the water from the hydroentangling step can be recycled also as discussed previously. Due to the low level of water- dispersible sulfopolyester, the sulfopolyester may not need to be removed from the wash water before reuse.
- the hydroentangling is conducted by water jets.
- the number of water jet heads can range from 1 to about 20, or from 2 to about 15, or 2 to about 10. Because a substantial amount of the sulfopolyester has been removed, the fibers contained in the microfiber web are much finer, and during the hydroentangling step, a superior nonwoven fabric is produced having a tighter configuration with less fraying and loose fibers.
- the hydroentangling process of this invention can be simplified over conventional nonwoven hydroentangling processes where hydroentangling occurs prior to removal of the water-dispersible polymer. Since the water non- dispersible polymer fibers in the microfiber web are finer, less hydraulic energy is needed to entangle the fibers. Furthermore, in conventional nonwoven processes, hydroentangling typically occurs prior to the removal of the water-dispersible sulfopolyester, and often times, further hydroentangling after removal of the sulfopolyester is required. However, in the present invention, a quality nonwoven fabric can be obtained without a further hydroentangling step.
- a process for making a nonwoven fabric comprising: (A) collecting multicomponent fibers to form a non- woven web; wherein the multicomponent fiber comprises at least one water dispersible sulfopolyester and at least one water non-dispersible polymer; wherein the multicomponent fiber has a plurality of domains comprising the water non- dispersible polymer; wherein the domains are substantially isolated from each other by the water dispersible sulfopolyester intervening between the domains; and
- the non-woven fabric can under go a heat setting step comprising heating the non- woven fabric to a temperature of at least about 100 0 C, and more preferably at least about 120°C.
- the heat setting step relaxes out internal fiber stresses and aids in producing a dimensionally stable fabric product. It is preferred that when the heat set material is reheated to the temperature to which it was heated during the heat setting step that it exhibits surface area shrinkage of less than about 5% of its original surface area. More preferably, the shrinkage is less than about 2% of the original surface area, and most preferably the shrinkage is less than about 1%.
- the nonwoven fabric can optionally be held together by 1) mechanical fiber cohesion and interlocking in a web or mat; 2) various techniques of fusing of fibers, including the use of binder fibers, utilizing the thermoplastic properties of certain polymers and polymer blends; 3) use of a binding resin such as starch, casein, a cellulose derivative, or a synthetic resin, such as an acrylic latex or urethane; 4) powder adhesive binders; or 5) combinations thereof.
- the fibers in the nonwoven fabric are often deposited in a random manner, although orientation in one direction is possible, followed by bonding using one of the methods described above.
- the instant invention produces nonwoven fabrics that can be utilized in clothing, curtains, upholstery, and uniforms.
- Nonwoven fabrics can also be utilized in personal care products, such as, but not limited to, wipes, feminine hygiene products, baby diapers, training pants, adult incontinence briefs, and hospital/surgical and other medical disposables, such as, but not limited to, surgical gowns, gauzes, bandages and the like.
- Other applications include, but are not limited to, multilayer nonwovens, laminates and composites, protective fabrics and layers, geotextiles, industrial wipes, and filter media.
- the fibrous articles may include replacement inserts for various personal hygiene and cleaning products.
- the fibrous article of the present invention may be bonded, laminated, attached to, or used in conjunction with other materials which may or may not be water-dispersible.
- the fibrous article for example, a nonwoven fabric layer, may be bonded to a flexible plastic film or backing of a water non-dispersible material, such as polyethylene.
- a water non-dispersible material such as polyethylene.
- the multicomponent fibers and nonwoven fabrics described in the following examples were produced in the manner described below.
- a pilot scale bicomponent spunbond line capable of producing a 0.5 meter wide nonwoven fabric was used to spin the multicomponent fibers and produce the nonwoven fabrics used in the listed examples.
- a simplified process diagram of the spunbond line is shown in Figure 1. The specific details of this process are described subsequently.
- Separate extruders and spin pumps were utilized to melt and meter the water dispersible sulfopolyester and the PET into the bicomponent spin pack. One extruder melted and metered the water dispersible sulfopolyester and the second extruder melted and metered the PET polymer.
- the water dispersible sulfopolyester was extruded at a melt temperature of 260°C, and the PET component was extruded at a 285°C melt temperature.
- the total combined polymer flow was about 1.33 kg/min., resulting in an average polymer flow rate exiting each die hole of about 0.60 grams/hole per minute from a spinneret having 2222 holes.
- An aspirator assembly using compressed air was utilized to form a high velocity downward flow stream which drew the extruded polymer melt streams exiting the spinneret into fine multicomponent fibers.
- sufficient air pressure was applied to draw the multicomponent fibers to a fineness of about 1.0 to about 1.5 denier per filament (dpf) or nominal filament diameters of about 8 to about 12 microns.
- the drawn fibers were laid down on a collection belt to form a continuous nonwoven web where the density (basis weight) of the nonwoven web was controlled by the speed of the belt and the extrusion rate.
- Nonwoven webs having a typical basis weight of about 100 to about 150 grams/sq. meter or as specified were produced in the examples.
- a compacting roll and wind up station was utilized to produce rolls of the lightly compacted nonwoven webs of multicomponent fibers with the segmented pie fiber cross-section structure.
- the compaction of the nonwoven web was conducted using calendar rolls at room temperature with sufficient nip pressure to consolidate the nonwoven web so it could be handled on a roll and unwound for further treatment.
- the nonwoven web produced by the preceding process was subsequently hydroentangled using a pilot scale hydroentangling line (manufactured by Fleissner , Engelsbach, Germany) having five hydroentangling heads.
- the hydroentangling equipment was utilized in the examples using different number of hydroentangling heads and pressures as specified in the examples.
- the hydroentangling equipment had three high pressure hydroentangling heads which contacted the nonwoven web as it passed under the water jets supported by a 103 mesh screen belt.
- the first head operated as a pre-wetting station using only about 30 bar water pressure while hydroentangling heads 2 and 3 were operated at a typical water pressure ranging from about 100 to about 200 bar.
- the water jets of the final two hydroentangling heads impacted the nonwoven web as it was conveyed on a hydroentangling drum with a porous surface capable of drawing the water from the hydroentangling jets into the drum using vacuum within the drum.
- These final two hydroentangling jets were operated at about 200 bar water pressure, and the jets contacted the side of the fabric opposite the side contacted by the first three hydroentangling jets.
- a jet strip was inserted which consisted of a line of finely machined holes having a diameter of about 120 microns with a separation between holes of about 0.8 mm.
- the water pressure of about 200 bar on one side of the jet strip inside the hydroentangling head caused a high velocity jet of water to be formed in each hole.
- These high velocity water jets caused the multicomponent fibers in the nonwoven web to entangle as the web passes under the hydroentangling jets.
- about 1200 water jets are applied per meter of nonwoven web width and typically the water flow through a jet strip is about 150 liters/minute or about 0.12 liter / min. of water flowing through each individual hole in the jet strip.
- the nonwoven web was passed under the hydroentangling jets at a speed ranging from about 10 meters/min. to about 50 meters/min.
- the fabric speed can be adjusted to vary the degree of hydroentangling treatment.
- the temperature of the water during the hydroentangling process was about 30°C - 40°C and no treatment of the process water such as deionization or demineralization was performed.
- the hydroentangling process water used in these examples was inherently low in metal ion content. In practice, demineralization of the water used in the hydroentangling operation is desirable.
- a nonwoven web comprised of bicomponent fibers having a segmented pie structure with 16 segments was prepared according to the procedure previously described.
- the non water dispersible component of the bicomponent fibers was F53HC grade of PET polyester with inherent viscosity of about 0.53 (Eastman Chemical Company, Kingsport, TN, U.S.A.) and extruded along with a water dispersible sulfopolyester as the second component.
- the water dispersible sulfopolyester had designation SP05F Lot TP06038931 (Eastman Chemical Company) and exhibited a melt viscosity of about 3000 poise as measured at 240°C and 1 rad/sec shear rate. Both polymers were extruded through a segmented pie bicomponent spin pack
- the nonwoven web of Example 1 was consolidated by pressing between calendar rolls at room temperature.
- the multicomponent fibers were melt drawn at an estimated speed in excess of about 5000 meters/min during this process.
- the nonwoven web of Example 1 was conditioned unrestricted in an oven at 120°C, the nonwoven web shrank to 60% x 57% of the starting dimensions in the MD (machine direction) and CD (cross direction) respectively due to stress relaxation of the multicomponent fibers.
- This nonwoven web had minimal inter- fiber bonding and served as the precursor for producing hydroentangled nonwoven fabrics by subsequent processing of this nonwoven web of Example 1.
- Example 2
- the nonwoven web of Example 1 was hydroentangled with high velocity water jets using a hydroentangling unit described previously. During the hydroentangling process, the fabric passed through the machine at a 40 meters / min. speed where the nonwoven web was exposed to two high pressure hydroentangling jets operating with 150 bar water pressure. The first jet was applied to the nonwoven web as it was transported on a 103 mesh screen belt to apply a fine mesh pattern to the nonwoven web. The second hydroentangling jet was applied to the opposite side of the web as it was supported on a hydroentangling drum operating under vacuum to yield the nonwoven fabric.
- the wet nonwoven fabric was passed through a drum dryer where 70°C air passed through the nonwoven fabric by the action of vacuum maintained within the 1.4 meter diameter drum.
- the nonwoven fabric was only partly dried when heated in the oven and exited in the wet state.
- the residence time of the nonwoven fabric in the oven was measured to be about 5 seconds.
- the nonwoven fabric was wound onto a core, some excess water was squeezed out, and it was noted that the water was cloudy due to the presence of emulsified sulfopolyester and also formed a sticky film when dried. Both observations indicated that some of sulfopolyester was emulsified during this drying step.
- the energy expended during the hydroentangling process is inversely proportional to the speed of the nonwoven fabric passing under the jets where slower speed translates to increased hydroentangling energy applied to the nonwoven fabric.
- the energy applied is directly proportional to the number of hydroentangling jet stations under which the nonwoven fabric passes where the hydroentangling energy applied by each jet station is proportional to the square root of the water pressure. Using these relationships, the relative amount of hydroentangling energy applied to a nonwoven web can be approximated for comparison.
- Example 2 the hydroentangling energy is arbitrarily assigned a value of 1.0, where in subsequent examples the value will represent the increase in hydroentangling energy applied to the nonwoven web relative to the process in Example 2
- the basis weight of the hydroentangled nonwoven fabric of Example 2 was
- Example 2 The wet nonwoven fabric of Example 2 was rinsed 3 times in ambient temperature deionized water to remove the sulfopolyester emulsified in the water phase soaked in the nonwoven fabric. After rinsing and drying, a soft nonwoven fabric was recovered. The nonwoven fabric recovered was very loose, exhibited limited strength, and had a fuzzy texture due to loose fiberson fabric surface. The nonwoven fabric had limited utility as a textile fabric. The weight loss during rinsing steps was 29% indicating about full removal of water dispersible sulfopolyester from the nonwoven fabric.
- Example 2 had limited utility as a finished product but consisted of a nonwoven web of microfibers where the sulfopolyester was removed from the multicomponent fibers to expose the PET microfibers. This precursor nonwoven fabric of Example 2 was further processed to make nonwoven fabrics ofsubsequent examples 5 and 7.
- Example 3
- the nonwoven web of Example 1 was hydroentangled with high velocity water jets using a hydroentangling unit described previously. During the hydroentangling process, the nonwoven web passed through the unit at 10 meters/min speed where the nonwoven web was exposed to four high pressure hydroentangling jets operating with jet pressures of 100 bar, 150 bar, 200 bar, and 200 bar, respectively. The first two jets were applied to the nonwoven web as it was transported on a 103 mesh screen belt to apply a fine mesh pattern to the nonwoven web. The third and fourth hydroentangling jets were applied to the opposite side of the nonwoven web as it was supported on a hydroentangling drum operating under vacuum to produce the nonwoven fabric.
- the wet nonwoven fabric was passed through a drum dryer where 70°C air passed through the nonwoven fabric by the action of vacuum maintained within the 1.4 meter diameter drum.
- the nonwoven fabric was only partly dried when heated in the oven and exited in the wet state.
- the residence time of the nonwoven fabric in the oven was measured to be about 18 seconds.
- As the nonwoven fabric was wound some excess water was squeezed out, and it was noted that the water was cloudy due to the presence of emulsified sulfopolyester.
- the emulsified sulfopolyester also formed a sticky film on the nonwoven fabric when dried.
- the energy expended during the hydroentangling process is inversely proportional to the speed of the nonwoven fabric passing under the jets where slower speed translates to increased hydroentangling energy applied to the nonwoven fabric.
- the energy applied is directly proportional to the number of hydroentangling jet stations under which the nonwoven fabric passes where the hydroentangling energy applied by each jet station is proportional to the square root of the water pressure.
- the relative amount of hydroentangling energy applied to this nonwoven web of Example 3 relative to Example 2 was calculated for comparison.
- the hydroentangling energy amounted to a value 8.3 times larger than the base value assigned to Example 2.
- the higher degree of hydroentanglement in Example 3 is due to 2 times the number of hydroentanglement jets used coupled with a 1 A process line speed which provided 4 times the residence time under the hydroentanglement jets.
- the basis weight of the hydroentangled nonwoven fabric of Example 3 was 136 gsm, which was similar to the value of the starting nonwoven web of Example 1 and indicated that none or only minimal amount of sulfopolyester was removed during hydroentangling.
- the wet nonwoven fabric of Example 3 was rinsed 3 times in ambient temperature deionized water to remove any sulfopolyester emulsified in the water phase soaked in the nonwoven fabric. After rinsing and drying, a soft nonwoven fabric was recovered. A weight loss of about 28% was observed indicating removal of essentially all of sulfopolyester from the nonwoven fabric.
- This nonwoven fabric was very flexible, exhibited good strength, but had a fuzzy surface texture due to loose surface fibers.
- This precursor fabric of Example 3 was used for further processing to make fabrics of Examples 6 and 9.
- Example 2 The wet nonwoven fabric of Example 2 was passed through a hydroentangling unit described previously using minimal water contact in order to remove the sulfopoyester from the nonwoven fabric without applying much additional entanglement of the multicomponent fibers in the fabric.
- the sulfopolyester in the nonwoven fabric was found to be present in the absorbed water phase rather than the multicomponent fibers, and a simple water rinse was found to remove the sulfopolyester from the nonwoven fabric.
- the nonwoven fabric passed through the hydroentangling unit at a 50 meters /min. speed where the nonwoven fabric was exposed to a single high pressure hydroentangling jets operating at 100 bar pressure. The temperature of the water during the process was about 20°C.
- Example 4 The fabric of Example 4 was dried at ambient temperatures and subsequently washed at 50°C in deionized water to calculate the amount of residual sulfopolyester in the nonwoven fabric that was not removed by the single water jet of the process of Example 4. Only a 3.0% weight loss was measured after washing the nonwoven fabric of Example 4 indicating that about 90% by weight of the sulfopolyester in the nonwoven fabric of Example 2 was removed by this single head hydroentangling step.
- the single water head was effective for removing the bulk of sulfopolyester in the nonwoven fabric and removal would have been more efficient if the temperature was higher, preferably in the range of about 40°C to about 50°C for sulfopolyester removal.
- Example 5 The precursor nonwoven fabric of Example 2 was further hydroentangled with high velocity water jets using the hydroentangling unit described previously. . During this subsequent second hydroentangling step, the precursor nonwoven fabric of Example 2 was passed through the hydroentangling unit at a speed of 10 meters /min and was exposed to four high pressure hydroentangling jets operating with jet pressures of 130 bar, 150 bar, 200 bar, and 200 bar respectively. The first two jets were applied to the nonwoven fabric as it was transported on a 61 mesh screen belt obtained from Asten Johnson in Charleston, SC to apply a mesh pattern to the nonwoven fabric. The third and fourth hydroentangling jets were applied to the opposite side of the nonwoven fabric as it was supported on a hydroentangling drum operating under vacuum.
- Example 5 the relative amount of hydroentangling energy applied to this nonwoven fabric in the process of Example 5 relative to the process of Example 2 was calculated for comparison.
- the hydroentangling energy in Example 5 amounts to a value 8.5 times larger than the base value of 1 assigned to Example 2.
- the overall hydroentanglement energy applied to the nonwoven fabric in the combined process of Example 2 and 5 amounts to a value about 9.5 times the hydroentangling energy applied in the process of Example 2 alone.
- This fabric exhibited very good fiber entanglement with no loose fibers on the surface. This fabric exhibited good smooth surface texture.
- Example 6 Example 6
- the precursor nonwoven fabric of Example 3 was further hydroentangled with high velocity water jets using the hydroentangling unit.
- the nonwoven fabric passed through the hydroentangling unit at a speed of 10 meters/min where the nonwoven fabric was exposed to four high pressure hydroentangling jets operating with jet pressures of 130 bar, 150 bar, 200 bar, and 200 bar, respectively.
- the first two jets were applied to the nonwoven fabric of Example 3 as it was transferred on a 61 mesh screen belt obtained from Asten Johnson to apply a mesh pattern to the fabric.
- the third and fourth hydroentangling jets were applied to the opposite side of the nonwoven fabric as it was supported on a hydroentangling drum operating under vacuum.
- Example 7 the relative amount of hydroentangling energy applied to this nonwoven fabric in the process of Example 6 relative to the process of Example 2 was calculated for comparison.
- the hydroentangling energy in Example 6 amounts to a value 8.5 times larger than the arbitrary value assigned to Example 2.
- the overall hydroentanglement energy applied to the nonwoven fabric in the combined process of Example 3 and 6 amounts to a value about 16.8 times the hydroentangling energy applied in the process of Example 2 alone.
- This fabric exhibited very good fiber entanglement with no loose fibers on the surface. This fabric exhibited good smooth surface texture.
- the precursor nonwoven fabric of Example 2 was further hydroentangled with high velocity water jets using the hydroentangling unit.
- the nonwoven fabric passed through the hydroentangling unit at a speed of 10 meters /min where the nonwoven fabric was exposed to four high pressure hydroentangling jets operating with jet pressures of 130 bar, 150 bar, 200 bar, and 200 bar, respectively.
- the first two jets were applied to the nonwoven fabric as it was transported on a Formtec 14 (14 mesh screen) belt obtained from Albany International in Albany, NY to apply a coarse mesh pattern to the nonwoven fabric.
- Example 5 The difference between the fabric of Example 5 and the fabric of Example 7 is the forming belt used, where the belt in Example 7 conferred a coarser basket weave appearance to the fabric surface compared to the fabric of Example 5.
- the third and fourth hydroentangling jets were applied to the opposite side of the nonwoven fabric as it was supported on a hydroentangling drum operating under vacuum.
- Example 7 the relative amount of hydroentangling energy applied to this nonwoven fabric in the process of Example 7 relative to the process of Example 2 was calculated for comparison.
- the hydroentangling energy in Example 7 amounts to a value 8.5 times larger than the arbitrary value of 1 assigned to Example 2.
- the overall hydroentanglement energy applied to the nonwoven fabric in the combined process of Example 2 and 7 amounts to a value about 9.5 times the hydroentangling energy applied in the process of Example 2 alone.
- This fabric exhibited very good fiber entanglement with no loose fibers on the surface. This fabric exhibited good smooth surface texture.
- Example 8
- the nonwoven fabric of Example 5 was heat set by placing pieces of fabric on a restraining frame and conditioning the nonwoven fabric in a forced air oven at 130°C for 5 minutes conditioning time.
- the restraining frame was a 14 inch x 14 inch frame with pins around the periphery of the frame, spaced with X A inch separation between pins. The restraining action of the pins prevented the nonwoven fabric from shrinking when heated.
- the conditioning at elevated temperature causes stress relaxation in the fibers.
- Example 6 The fabric of Example 6 was heat set by placing pieces of nonwoven fabric on a restraining frame and conditioning the nonwoven fabric in a forced air oven at 130°C for 5 minutes conditioning time.
- the restraining frame was a 14 inch x 14 inch frame with pins around the periphery of the frame, spaced with Vi inch separation between pins. The restraining action of the pins prevented the nonwoven fabric from shrinking when heated.
- the conditioning at elevated temperature causes stress relaxation in the fibers.
- the nonwoven fabric of Example 7 was heat set by placing pieces of nonwoven fabric on a restraining frame and conditioning the nonwoven fabric in a forced air oven at 130°C for 5 minutes conditioning time.
- the restraining frame was a 14 inch x 14 inch frame with pins around the periphery of the frame, spaced with Vi inch separation between pins. The restraining action of the pins prevented the nonwoven fabric from shrinking when heated.
- the conditioning at elevated temperature causes stress relaxation in the fibers.
- Example 1 The fabric of Example 1 was hydroentangled with high velocity water jets using the hydroentangling unit described previously. During the hydroentangling process the fabric passed through the machine at a 10 meters / min. speed where the nonwoven web was exposed to four high pressure hydroentangling jets operating with jet pressures of 100 bar, 150 bar, 200 bar, and 200 bar respectively. The first two jets were applied to the fabric as it was transferred on a 103 mesh screen belt to apply a fine mesh pattern to the fabric. The third and fourth hydroentangling jets were applied to the opposite side of the web as it was supported on a hydroentangling drum operating under vacuum.
- the wet fabric was passed through a drum dryer where 70°C air passed through the fabric by the action of vacuum maintained within the 1.4 meter diameter drum.
- the fabric was only partly dried when heated in the oven and exited in the wet state.
- the residence time of the fabric in the oven was measured to be about 18 seconds.
- As the fabric was wound onto a core some excess water was squeezed out and it was noted that the water was cloudy indicating some emulsification of sulfopolyester.
- the fabric formed by this hydroentangling step was rinsed in both in deionized water at 45°C and in a home washing machine using a hot water (48°C) cycle.
- the fabric had a highly wrinkled appearance with a large number of loose fibers on the surface.
- the fabric was very "tacky” or “clingy” due to the loose nature of the surface fibers in the fabric and not desirable for textile applications.
- Comparative Example 2 The nonwoven fabric of Comparitive Example 1 was heat set by placing pieces of fabric on a restraining frame and conditioning the nonwoven fabric in a forced air oven at 130 0 C for 5 minutes conditioning time.
- the restraining frame was a 14 inch x 14 inch frame with pins around the periphery of the frame, spaced with 1 A inch separation between pins.
- the restraining action of the pins prevented the nonwoven fabric from shrinking when heated..
- the conditioning at elevated temperature causes stress relaxation in the fibers..
- This fabric exhibited loose fibers on the surface and had "tacky” or “clingy” feel due the excessive amount of loose fibers on the surface.
Abstract
Description
Claims
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JP2009544837A JP2010514957A (en) | 2007-01-03 | 2007-12-17 | Nonwoven fabric made from multicomponent fiber containing sulfopolyester |
EP07863010A EP2099962A2 (en) | 2007-01-03 | 2007-12-17 | Nonwovens fabrics produced from multicomponent fibers comprising sulfopolyesters |
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US11/648,953 US20080160859A1 (en) | 2007-01-03 | 2007-01-03 | Nonwovens fabrics produced from multicomponent fibers comprising sulfopolyesters |
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EP (1) | EP2099962A2 (en) |
JP (1) | JP2010514957A (en) |
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CN (1) | CN101573481A (en) |
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Also Published As
Publication number | Publication date |
---|---|
CN101573481A (en) | 2009-11-04 |
WO2008085332A3 (en) | 2009-02-12 |
KR20090096620A (en) | 2009-09-11 |
TW200840895A (en) | 2008-10-16 |
EP2099962A2 (en) | 2009-09-16 |
JP2010514957A (en) | 2010-05-06 |
US20080160859A1 (en) | 2008-07-03 |
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