US20080120758A1 - Thermal impulse bonding of thermally sensitive laminate barrier materials - Google Patents

Thermal impulse bonding of thermally sensitive laminate barrier materials Download PDF

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Publication number
US20080120758A1
US20080120758A1 US11/512,455 US51245506A US2008120758A1 US 20080120758 A1 US20080120758 A1 US 20080120758A1 US 51245506 A US51245506 A US 51245506A US 2008120758 A1 US2008120758 A1 US 2008120758A1
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United States
Prior art keywords
bond
film
gown
layer
film layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US11/512,455
Inventor
Mary Katherine Lawson
Michael P. Mathis
John Anthony Rotella
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Kimberly Clark Worldwide Inc
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Kimberly Clark Worldwide Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kimberly Clark Worldwide Inc filed Critical Kimberly Clark Worldwide Inc
Priority to US11/512,455 priority Critical patent/US20080120758A1/en
Assigned to KIMBERLY-CLARK WORLDWIDE, INC. reassignment KIMBERLY-CLARK WORLDWIDE, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ROTELLA, JOHN A., LAWSON, MARY K., MATHIS, MICHAEL P.
Priority to EP07805048A priority patent/EP2053933A1/en
Priority to PCT/IB2007/052602 priority patent/WO2008026090A1/en
Priority to MX2009001211A priority patent/MX2009001211A/en
Priority to CA002661816A priority patent/CA2661816A1/en
Priority to AU2007290926A priority patent/AU2007290926A1/en
Publication of US20080120758A1 publication Critical patent/US20080120758A1/en
Abandoned legal-status Critical Current

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    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D13/00Professional, industrial or sporting protective garments, e.g. surgeons' gowns or garments protecting against blows or punches
    • A41D13/12Surgeons' or patients' gowns or dresses
    • A41D13/1209Surgeons' gowns or dresses
    • AHUMAN NECESSITIES
    • A41WEARING APPAREL
    • A41DOUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
    • A41D27/00Details of garments or of their making
    • A41D27/24Hems; Seams
    • A41D27/245Hems; Seams made by welding or gluing
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    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
    • B29C48/03Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
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    • B29C48/00Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
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    • B29C65/02Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
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    • B29C65/02Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
    • B29C65/38Impulse heating
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    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29C66/9141Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux by controlling or regulating the temperature
    • B29C66/91411Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux by controlling or regulating the temperature, the heat or the thermal flux by controlling or regulating the temperature of the parts to be joined, e.g. the joining process taking the temperature of the parts to be joined into account
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/90Measuring or controlling the joining process
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    • B29C66/919Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29C66/00General aspects of processes or apparatus for joining preformed parts
    • B29C66/90Measuring or controlling the joining process
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    • B29C66/9192Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges in explicit relation to another variable, e.g. temperature diagrams
    • B29C66/91921Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges in explicit relation to another variable, e.g. temperature diagrams in explicit relation to another temperature, e.g. to the softening temperature or softening point, to the thermal degradation temperature or to the ambient temperature
    • B29C66/91931Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges in explicit relation to another variable, e.g. temperature diagrams in explicit relation to another temperature, e.g. to the softening temperature or softening point, to the thermal degradation temperature or to the ambient temperature in explicit relation to the fusion temperature or melting point of the material of one of the parts to be joined
    • B29C66/91935Measuring or controlling the joining process by measuring or controlling the temperature, the heat or the thermal flux characterised by specific temperature, heat or thermal flux values or ranges in explicit relation to another variable, e.g. temperature diagrams in explicit relation to another temperature, e.g. to the softening temperature or softening point, to the thermal degradation temperature or to the ambient temperature in explicit relation to the fusion temperature or melting point of the material of one of the parts to be joined lower than said fusion temperature
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    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
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    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/04Polymers of ethylene
    • B29K2023/06PE, i.e. polyethylene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/10Polymers of propylene
    • B29K2023/12PP, i.e. polypropylene
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2101/00Use of unspecified macromolecular compounds as moulding material
    • B29K2101/12Thermoplastic materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/0085Copolymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/06Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts
    • B29K2105/08Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts of continuous length, e.g. cords, rovings, mats, fabrics, strands or yarns
    • B29K2105/0854Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts of continuous length, e.g. cords, rovings, mats, fabrics, strands or yarns in the form of a non-woven mat
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2105/00Condition, form or state of moulded material or of the material to be shaped
    • B29K2105/06Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts
    • B29K2105/16Fillers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0037Other properties
    • B29K2995/0065Permeability to gases
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2995/00Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
    • B29K2995/0037Other properties
    • B29K2995/0068Permeability to liquids; Adsorption
    • B29K2995/0069Permeability to liquids; Adsorption non-permeable
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2009/00Layered products
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29LINDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
    • B29L2031/00Other particular articles
    • B29L2031/48Wearing apparel
    • B29L2031/4842Outerwear
    • B29L2031/485Jackets

Definitions

  • the over garment is typically a gown that has a main body portion to which sleeves and a tie cord are attached.
  • the tie cord encircles the wearer at the waist to keep the gown in place.
  • the surgical gown prevents bodily fluids and other liquids present during surgical procedures from flowing through the gown.
  • Surgical gowns were originally made of cotton or linen, were reusable and were sterilized prior to each use in the operating room.
  • a disadvantage of the materials used in these types of gowns is that they tend to form lint, which is capable of becoming airborne or clinging to the clothes of the wearer, thereby providing another potential source of contamination. Additionally, costly laundering and sterilization procedures were required before reuse.
  • Disposable surgical gowns have largely replaced the reusable linen surgical gown and many are now made in part or entirely from fluid repellent or impervious fabrics to prevent liquid penetration or “strike through”.
  • Various materials and designs have been used in the manufacture of surgical gowns to prevent contamination in different operating room conditions.
  • Surgical gowns are now available in a variety of different levels of imperviousness and comfort.
  • Gowns made from completely impervious material provide a high degree of protection, though a surgical gown constructed of this type of material is typically heavy, expensive, and uncomfortably hot to the wearer.
  • certain portions such as the shoulders and back panels may be of a lighter weight material in order to provide for better breathability and help reduce the overall weight of the gown.
  • the higher the breathability of the material the lower the repellency of the material.
  • AAMI level 4 used in “critical zones” where exposure to blood or other bodily fluids is most likely and voluminous.
  • the AAMI standards define “critical zones” as the front of the gown, including the tie cord attachment area, and the sleeves and sleeve seam area up to about 2 inches (5 cm) above the elbow.
  • the main body portion and the sleeves of a surgical gown are usually produced separately and joined together in some manner at seams in the shoulder area.
  • the sleeves are commonly made from a flat piece of fabric that is folded upon itself and joined together at a seam that runs the length of the sleeve from the shoulder to the wrist, prior to attachment to the main body portion.
  • a single tie cord or a pair of tie cords is also usually attached to the main body portion of the gown.
  • a single tie cord is used to encircle the wearer at the waist and tie to itself in order to keep the gown in position during use.
  • Two tie cords are also used to encircle the wearer at the waist and tie to each other.
  • the seams and the tie cord attachment point are areas where many gowns have been known to fail the AAMI test procedure.
  • Ultrasonic seam sealing bonds the layers of material together sufficiently for strength but the bonds do not pass ASTM-1671-b; the bacteriophage penetration resistance test, a test that is now required to meet the new AAMI level 4 protection standards. This is particularly true for the sleeve seams and tie cord attachment point.
  • FIG. 1 illustrates an exemplary gown 100 to be worn during a medical procedure as seen from the front.
  • FIG. 2 illustrates an exemplary gown 100 to be worn during a medical procedure as seen from the back.
  • FIG. 3 represents a exemplary tie cord for a surgical gown.
  • thermal impulse heat welding aka “bar sealing”
  • thermally sensitive laminate barrier materials made of thermoplastic polymers such that they will pass AAMI level 4 testing (ASTM 1670 and 1671-b).
  • AAMI level 4 testing ASTM 1670 and 1671-b.
  • bar sealing overlapping layers of thermally sensitive barrier materials composed of thermoplastic polymers are melted and fused together to create a substantially solid bond at the surface of the materials. No substantially un-melted areas remain within the fused seam area on the surface.
  • the present invention involves the use of bar sealing technology to meet AAMI level 4 barrier properties in surgical gowns and similar articles formed from thermally sensitive laminate barrier materials that are composed of thermoplastic polymers.
  • thermally sensitive laminate barrier materials that are composed of thermoplastic polymers.
  • overlapping layers of these thermally sensitive laminate barrier materials are melted and fused together to create a substantially solid bond at the surface of the materials while avoiding damage to regions below the surface of the laminate. No substantially un-melted areas remain within the fused bond area on the surface where heat was applied.
  • FIG. 1 illustrates a typical gown 100 to be worn during a medical procedure as seen from the front.
  • the gown 100 includes a collar 110 , the cuffs 120 , the primary tie cord 130 and a primary tie cord attachment area 140 .
  • the shoulder seams 150 linking the sleeves 160 to the main body 170 are also visible.
  • FIG. 2 illustrates a typical gown 100 to be worn during a medical procedure as seen from the back. In FIG. 2 the shoulder seams 150 linking the sleeves 160 the main body 170 are visible as are the sleeve seams 180 running from the shoulder seams 150 to the cuffs 120 which are used to produce the sleeves 160 .
  • FIG. 2 also shows a secondary tie cord 180 and secondary tie attachment area 190 (not in the AAMI critical zone).
  • FIG. 1 illustrates a typical gown 100 to be worn during a medical procedure as seen from the front.
  • the gown 100 includes a collar 110 , the cuffs 120 , the primary tie cord 130 and a primary tie cord attachment area 140 .
  • FIG. 3 represents the tie cord 130 and shows the end to be bonded to the gown 100 as having, in this case, a “Y” shaped end 200 for attachment to the gown 100 .
  • a simple flat shaped end may also be used for attachment to the gown, a “Y” shape is not required.
  • barrier materials composed of thermoplastic polymers. While such barrier materials may be in the form of thermoplastic polymer spunbond fabrics, thermoplastic polymer meltblown fabrics, and various combinations of such spunbond and meltblown fabrics, a particularly desirable form of these barrier materials incorporate one or more thin, breathable films that provide desirable levels of resistance to penetration by liquids and pathogens while also providing satisfactory levels of breathability and/or moisture vapor transmission.
  • thermoplastic polyolefins like polyethylene and polypropylene and copolymers thereof because of their relatively low cost and ability to be processed.
  • Polyethylene is generally used in the film production and the film is commonly “filled” with calcium carbonate, various kinds of clay, silica, alumina, barium carbonate, soldium carbonate, magnesium carbonate, talc, barium sulfate, magnesium sulfate, aluminum sulfate, titanium dioxide, zeolites, cellulose-type powders, kaolin, mica, carbon, calcium oxide, magnesium oxide, aluminum hydroxide, pulp powder, wood powder, cellulose derivatives, chitin and chitin derivatives, to increase breathability.
  • the breathable films of barrier laminate are frequently compromised such that they so longer provide desired levels of barrier to liquid penetration and pathogens.
  • the thin and breathable film laminates described above may be thermally bonded using bar sealing, thus producing a thermal bond for a film layer-containing thermoplastic fabric where the bond joins a thermoplastic material to the fabric to form a fused bonded area, without bonding to the film layer. This bond has no un-melted areas remaining within the fused bond area on the surface.
  • spunbond refers to fabric made from small diameter fibers which are formed by extruding molten thermoplastic material as filaments from a plurality of fine, usually circular capillaries of a spinneret with the diameter of the extruded filaments then being rapidly reduced as by, for example, in U.S. Pat. No. 4,340,563 to Appel et al., and U.S. Pat. No. 3,692,618 to Dorschner et al., U.S. Pat. No. 3,802,817 to Matsuki et al., U.S. Pat. Nos. 3,338,992 and 3,341,394 to Kinney, U.S. Pat. No. 3,502,763 to Hartman, and U.S. Pat.
  • Spunbond fibers are generally not tacky when they are deposited onto a collecting surface. Spunbond fibers are generally continuous and have average diameters (from a sample of at least 10) larger than 7 microns, more particularly, between about 10 and 20 microns.
  • Meltblown fabric is formed by extruding a molten thermoplastic material through a plurality of fine, usually circular, die capillaries as molten threads or is filaments into converging high velocity, usually hot, gas (e.g. air) streams which attenuate the filaments of molten thermoplastic material to reduce their diameter, which may be to microfiber diameter.
  • the meltblown fibers are then carried by the high velocity gas stream and are deposited on a collecting surface to form a web of randomly dispersed meltblown fibers.
  • Such a process is disclosed, for example, in U.S. Pat. No. 3,849,241 to Butin et al.
  • Meltblown fibers are microfibers which may be continuous or discontinuous, are generally smaller than 10 microns in average diameter, and are generally tacky when deposited onto a collecting surface.
  • Laminates of spunbond and meltblown fabrics e.g., spunbond/meltblown/spunbond (SMS) laminates and others are disclosed in U.S. Pat. No. 4,041,203 to Brock et al., U.S. Pat. No. 5,169,706 to Collier, et al, U.S. Pat. No. 5,145,727 to Potts et al., U.S. Pat. No. 5,178,931 to Perkins et al. and U.S. Pat. No. 5,188,885 to Timmons et al.
  • SMS spunbond/meltblown/spunbond
  • Such a laminate may be made by sequentially depositing onto a moving forming belt first a spunbond fabric layer, then a meltblown fabric layer and last another spunbond layer and then bonding the laminate in a manner described below.
  • the fabric layers may be made individually, collected in rolls, and combined in a separate bonding step.
  • Such fabrics usually have a basis weight of from about 0.1 to 12 osy (6 to 400 gsm), or more particularly from about 0.75 to about 3 osy.
  • Multilayer laminates may also have various numbers of meltblown layers or multiple spunbond layers in many different configurations and may include other materials like films (F) or coform materials, e.g. SMMS, SM, SFS, etc.
  • An exemplary method of forming a film includes a co-extrusion film apparatus that forms the film with multiple layers consisting of skin and core layers.
  • the apparatus will include two or more polymer extruders.
  • the film is extruded into a pair of nip or chill rollers.
  • the film is extruded onto a chilled roll which can have a smooth or matte finish.
  • the film as initially formed will have an overall thickness of approximately 25 to 60 micrometers with, in the case of multilayer films, the total skin or bonding layer having an initial thickness that may be about 3% to 30% of the total thickness.
  • Other film making processes known to those skilled in the art may be used as well, including cast embossing, chill and flat casting and blown film processes.
  • the film is directed to a film stretching unit such as a machine direction orienter (MDO), which is a commercially available device from vendors such as the Marshall and Williams Company of Buffalo, R.I.
  • MDO machine direction orienter
  • Such an apparatus has a plurality of paired stretch rolls that move at predetermined speeds that may rotate faster, slower or at the same speed relative to each other.
  • the stretch rolls move at a progressively faster speeds to progressively stretch and thin the film in the machine direction of the film, which is the direction of travel of the film through the process.
  • the stretch rolls are generally heated for processing advantages.
  • the temperatures to which the film is heated while stretching will depend on the composition of the film as well as the breathability and other desired end properties of the laminate. In most cases the film will be heated to a temperature no higher than 5 degrees ° C. below the melting point of the core or “B” layer in the film.
  • the purpose for heating the film is to allow it to be stretched quickly without causing film defects.
  • the amount of stretching will depend on the polymeric composition, but, in general, the film may be stretched to about 300% or more of its original length (that is, a one cm length, for example, will be stretched to 3 cm) but less than the amount that tends to result in film defects. For most applications, for example, the stretch will be to at least 200% of the original film length and, frequently, in the range of about 250% to 500%.
  • the multilayer stretch-thinned film may be attached to one or more support layers to form a multilayer film/nonwoven laminate as described above.
  • a conventional fibrous nonwoven web forming apparatus such as a pair of spunbond machines, may be used to form the support layer.
  • the long, essentially continuous fibers are deposited onto a forming wire as an unbonded web and the unbonded web is then sent through a pair of bonding rolls to bond the fibers together and increase the tear strength of the resultant web support layer.
  • One or both of the rolls are often heated to aid in bonding.
  • one of the rolls is also patterned so as to impart a discrete bond pattern with a prescribed bond surface area to the web.
  • the other roll is usually a smooth anvil roll but this roll also may be patterned if so desired.
  • the two layers are brought together and laminated to one another using a pair laminating rolls or other means.
  • the laminating rolls may be heated.
  • at least one of the rolls may be patterned to create a discrete bond pattern with a prescribed bond surface area for the resultant laminate.
  • the maximum bond point surface area for a given area of surface on one side of the laminate will not exceed about 50 percent of the total surface area.
  • the process described above may be used to create a three layer laminate.
  • the only modification to the previously described process is to feed a supply of a second fibrous nonwoven web support layer into the laminating roll on a side of the multilayer film opposite that of the other fibrous nonwoven web support layer.
  • the support layer may be formed directly in-line. In either event, the second support layer is fed into the laminating rolls and is laminated to the multilayer film in the same fashion as the other support layer.
  • Multilayer film laminates may have various numbers of meltblown layers or multiple spunbond layers in many different configurations and may include other materials like coform materials. These include, for example, spunbond/film/spunbond (SFS) laminates, spunbond/film/meltblown (SFM) laminates, spunbond/meltblown/film (SMF) laminates and laminates having a greater number of layers like spunbond/film/spunbond/meltblown/spunbond (SFSMS) and spunbond/meltblown/film/meltblown/spunbond SMFMS, coform/meltblown/film (CMF) etc.
  • FSS spunbond/film/spunbond
  • SFM spunbond/film/meltblown
  • SMF spunbond/meltblown/film
  • CMF coform/meltblown/film
  • thermally sensitive materials means fabrics and webs which have a tendency to become compromised by heat and/or or pressure. These materials have a relatively narrow range of temperature (the bonding window) at which they can be bonded and can be damaged to a great degree when conditions fall outside of these ranges.
  • a “substantially solid bond” is one in which there are no substantially un-melted areas within the bond footprint. This means that the thermoplastic fibers on the surface have been melted to a degree sufficient to produce a film. The surface film thus produced is the material which results in a bonding together of the two layers that are desired to be bonded.
  • bar sealing can bond a thermoplastic material to a second thermoplastic material that has a film layer within it, without damaging the barrier properties of the film layer. Bar sealing is also substantially less expensive and less challenging in a manufacturing environment than is adhesive bonding.
  • Bar sealing uses heat, pressure and dwell time to thermally bond thermoplastic materials together. According to the present invention, these variables are adjusted so that the thermal bonding takes place substantially at or adjacent the surface of the thermally sensitive barrier laminate materials while avoiding degradation of the thermally sensitive film component in an interior region of the barrier laminate.
  • Bar sealing devices generally have a press with a set of jaws that open (vertically), into which the materials to be bonded are placed.
  • the jaws are heated by, for example, electric resistance heating and the temperature of each may be controlled separately.
  • the pressure at which the jaws come together may also be adjusted for optimal bonding.
  • the time for which the jaws are together (the “dwell” or “hover” time) may also be adjusted. A dwell time of zero indicates that the jaws were brought together for an instant and immediately moved apart, i.e., they were not held together.
  • jaw size is generally about a 1.75 cm (a half inch) wide, producing a bond width of about 0.635 cm (1 ⁇ 4 inch), by about 3.8 cm long (1.5 inches) to about 6.35 cm (2.5 inches) long.
  • the jaw size may be as small as a half centimeter by a centimeter, depending on the materials to be joined.
  • An exemplary bar sealing device is available from Therm-O-Seal® Corporation of Mansfield, Tex.
  • One such device is a Vertrod® Style Steel frame sealer that has jaws about 1.75 cm wide and 2.54 cm in length and uses electrical resistance heating and water cooling.
  • Another is a Vertrod® style hand-held heat sealer that can produce a bond of 2, 4, 8 or 12 inches (5.1, 10.16, 20.3 and 30.5 cm) in length and 1 ⁇ 8, 3/16, 1 ⁇ 4 and 3 ⁇ 8 inch (0.32, 0.48, 0.64 and 0.95 cm) in width.
  • a bar sealing device is a Vertrod® style table-top vacuum heat sealer producing seals 9, 14, 20, 24 and 30 inches (22.9, 35.6, 50.8, 61 and 76.2 cm) in length and 1 ⁇ 8, 3/16, 1 ⁇ 4 and 3 ⁇ 8 inch in width.
  • thermoplastic polymeric materials commonly used in disposable gowns and for components such as, for example, tie cords that are presently attached to such disposable gowns are typically nonwoven fabrics formed from polypropylene and/or polyethylene and have a basis weight typically ranging from about 0.5 (17 gsm) to about 1.5 osy (51 gsm).
  • the tie cord material may be a folded 1.0 osy (34 gsm) SMS material made as described above.
  • Fabric for the fabrication of gowns may be, for example, made of random copolymer spunbond, a three layer (Catalloy®/polyethylene/Catalloy®) or “ABA” calcium carbonate filled film, and a spunbond/meltblown/spunbond (SMS) layer.
  • This “SFSMS” may bonded together to form the gown with the SMS against the skin.
  • the spunbond layer and film may have a basis weight of between 0.2 and 1.0 osy (7 and 34 gsm) or more particularly about 0.6 osy (20.3 gsm).
  • the SMS layer may have a basis weight of between 0.5 and 1.5 osy (17 and 51 gsm) or more particularly about 0.75 osy (25.4 gsm).
  • the temperature of the bar sealer should be between 240 and 320° F. (116 and 160° C.), the pressure should be between 40 and 80 psi (276 and 552 kPa) and the dwell time should be between 0 and 5 seconds. More particularly, the temperature should be between 260 and 290° F. (127 and 143° C.), the pressure should be between 50 and 60 psi (345 and 414 kPa) and the dwell time should be between 1 and 3 seconds.
  • the test uses a penetration test cell available from Wilson Road Machine Shop, Rising Sun, Md.
  • the cell has a capacity of about 60 ml.
  • the specimen acts as a partition separating the challenge fluid from the viewing side of the penetration cell.
  • An annular flange cover with an open area to allow visual observations of the specimen, and a transparent cover are included.
  • the cell body has top port for filling and a drain valve for draining the penetration test cell.
  • Test Method F903 Test Method for testing.
  • the fabric specimen is placed in the penetration cell with the layer that is normally outermost facing the back (solid flange) part of the cell where the challenge fluid is placed.
  • the cell is filled through the top port with the challenge fluid and observed for 5 minutes. Air is then supplied to the top port and the sample held at 13.8 kPa (2 psig) for 1 minute and the pressure released. If liquid penetration is not yet seen, the sample is allowed to stand for 54 minutes and observed. If bacteriophage is the test fluid, the sample is subsequently assayed using a 0.5 ml sample size onto agar for 6 to 18 hours at 35 to 37° C. to test for passage of fluid that is not observable to the unaided eye.
  • Kimberly-Clark MicroCool® surgical gowns are made of random copolymer spunbond, a three layer (Catalloy®/polyethylene/Catalloy®) calcium carbonate filled film, and a spunbond/meltblown/spunbond (SMS) layer.
  • This “SFSMS” is bonded together to form the gown with the SMS against the skin.
  • the random copolymer of which the outermost layer of spunbond material is made is a 2.5 weight percent ethylene-propylene copolymer known as R532-35R, from the Dow Chemical Company of Midland, Ml. No treatments are applied to the fabric.
  • the spunbond layer and film each had a basis weight of 0.6 osy (20.3 gsm).
  • the SMS layer had a basis weight of 0.75 osy (25.4 gsm).
  • the tie cord to be bonded to the gown was a folded 1.0 osy (34 gsm) SMS material.
  • the material was folded either once for a double layer of fabric, or twice for a triple layer of fabric.
  • the outer layer (spunbond) was made from a 2.5 weight percent ethylene-propylene copolymer known as R532-35R, from the Dow Chemical Company and the outer layer is treated with an antistat and a fluorochemical to reduce surface tension.
  • a additional piece of tie cord material was bonded to the tie cord near an end to produce a “Y” shaped end for bonding to the gown on both upper end of the Y.
  • the Y was flattened out onto the gown for bonding at two points on the branches of the Y but near the stem of the Y.
  • a bar sealing device from Therm-O-Seal® of Mansfield, Tex. was used. It was a Vertrod® model number 2PF-ST-12004-55HT-WC-CRF-TC-KY-SP. This device had jaws about 1.75 cm wide and 2.54 cm in length and used electrical resistance heating and water cooling. Only the jaw in contact with the tie cord was heated.
  • a double folded SMS tie cord was bonded to a MicroCool® surgical gown at a temperature of 275 to 282° F. (135 to 139° C.) at a zero dwell time and 56 psi pressure (386 kPa). The bonded area was tested according to ASTM 1670. Nine out of 11 samples passed and two failed.
  • a double folded SMS tie cord was bonded to a MicroCool® surgical gown at a temperature of 280 to 286° F. (138 to 141° C.) at a zero dwell time and 56 psi pressure (386 kPa). The bonded area was tested according to ASTM 1670. All 11 samples passed
  • a double folded SMS tie cord was bonded to a MicroCool® surgical gown at a temperature of 290 to 296° F. (143 to 147° C.) at a zero dwell time and 56 psi pressure (386 kPa). The bonded area was tested according to ASTM 1670. Nine out of 11 samples passed and two failed.
  • Example 2 The samples from Example 2 were tested according to ASTM 1671-b using bacteriophage. Eleven of 11 samples passed.

Abstract

Thermal impulse heat welding, or “bar sealing”, is used to bond thermally sensitive laminate barrier materials such that they will pass AAMI level 4 testing (ASTM 1670 and 1671-b). In bar sealing, overlapping layers of thermally sensitive laminate barrier materials are melted and fused together to create a substantially solid bond at and/or adjacent the surface. No substantially un-melted areas remain within the fused bond area on the surface.

Description

    BACKGROUND OF THE INVENTION
  • Surgeons and other healthcare providers often wear an over garment during operating procedures in order to enhance the sterile condition in the operating room and to protect the wearer. The over garment is typically a gown that has a main body portion to which sleeves and a tie cord are attached. The tie cord encircles the wearer at the waist to keep the gown in place. In order to prevent the spread of infection to and from the patient, the surgical gown prevents bodily fluids and other liquids present during surgical procedures from flowing through the gown.
  • Surgical gowns were originally made of cotton or linen, were reusable and were sterilized prior to each use in the operating room. A disadvantage of the materials used in these types of gowns is that they tend to form lint, which is capable of becoming airborne or clinging to the clothes of the wearer, thereby providing another potential source of contamination. Additionally, costly laundering and sterilization procedures were required before reuse.
  • Disposable surgical gowns have largely replaced the reusable linen surgical gown and many are now made in part or entirely from fluid repellent or impervious fabrics to prevent liquid penetration or “strike through”. Various materials and designs have been used in the manufacture of surgical gowns to prevent contamination in different operating room conditions. Surgical gowns are now available in a variety of different levels of imperviousness and comfort.
  • Gowns made from completely impervious material provide a high degree of protection, though a surgical gown constructed of this type of material is typically heavy, expensive, and uncomfortably hot to the wearer. In some surgical gowns, certain portions such as the shoulders and back panels may be of a lighter weight material in order to provide for better breathability and help reduce the overall weight of the gown. Generally, however, the higher the breathability of the material, the lower the repellency of the material.
  • Different types of surgical procedures expose the healthcare provider to different levels of blood and/or fluid exposure, so it is not feasible or economical to use the same type of surgical gown for every surgical procedure conducted by the healthcare provider. New guidelines have recently been created for the rating of the imperviousness of surgical gowns, gloves and the like, to provide guidance to healthcare providers. The Association for the Advancement of Medical Instrumentation (AAMI) has proposed a uniform classification system for gowns and drapes based on their liquid barrier performance. These procedures were adopted by the American National Standards Institute (ANSI) and were recently published as ANSIA/AAMI PB70: 2003 entitled Liquid Barrier Performance and Classification of Protective Apparel and Drapes Intended for Use in Health Care Facilities, which was formally recognized by the U.S. Food and Drug Administration in October, 2004. This standard established four levels of barrier protection for surgical gowns and drapes. The requirements for the design and construction of surgical gowns are based on the anticipated location and degree of liquid contact, given the expected conditions of use of the gowns. The highest level of imperviousness is AAMI level 4, used in “critical zones” where exposure to blood or other bodily fluids is most likely and voluminous. The AAMI standards define “critical zones” as the front of the gown, including the tie cord attachment area, and the sleeves and sleeve seam area up to about 2 inches (5 cm) above the elbow.
  • The main body portion and the sleeves of a surgical gown are usually produced separately and joined together in some manner at seams in the shoulder area. The sleeves are commonly made from a flat piece of fabric that is folded upon itself and joined together at a seam that runs the length of the sleeve from the shoulder to the wrist, prior to attachment to the main body portion. A single tie cord or a pair of tie cords is also usually attached to the main body portion of the gown. A single tie cord is used to encircle the wearer at the waist and tie to itself in order to keep the gown in position during use. Two tie cords are also used to encircle the wearer at the waist and tie to each other. The seams and the tie cord attachment point are areas where many gowns have been known to fail the AAMI test procedure.
  • A number of surgical gowns are currently marketed which are assembled through the use of ultrasonic seam sealing. Ultrasonic seam sealing bonds the layers of material together sufficiently for strength but the bonds do not pass ASTM-1671-b; the bacteriophage penetration resistance test, a test that is now required to meet the new AAMI level 4 protection standards. This is particularly true for the sleeve seams and tie cord attachment point.
  • It is clear that there exists a need for a gown having tie cord attachments bonded in a manner that is more impervious than current methods and that meets AAMI level 4.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 illustrates an exemplary gown 100 to be worn during a medical procedure as seen from the front.
  • FIG. 2 illustrates an exemplary gown 100 to be worn during a medical procedure as seen from the back.
  • FIG. 3 represents a exemplary tie cord for a surgical gown.
  • SUMMARY OF THE INVENTION
  • In response to the foregoing difficulties encountered by those of skill in the art, we have successfully used thermal impulse heat welding, aka “bar sealing”, to bond thermally sensitive laminate barrier materials made of thermoplastic polymers such that they will pass AAMI level 4 testing (ASTM 1670 and 1671-b). In bar sealing, overlapping layers of thermally sensitive barrier materials composed of thermoplastic polymers are melted and fused together to create a substantially solid bond at the surface of the materials. No substantially un-melted areas remain within the fused seam area on the surface.
  • DETAILED DESCRIPTION OF THE INVENTION
  • The present invention involves the use of bar sealing technology to meet AAMI level 4 barrier properties in surgical gowns and similar articles formed from thermally sensitive laminate barrier materials that are composed of thermoplastic polymers. In bar sealing, overlapping layers of these thermally sensitive laminate barrier materials are melted and fused together to create a substantially solid bond at the surface of the materials while avoiding damage to regions below the surface of the laminate. No substantially un-melted areas remain within the fused bond area on the surface where heat was applied.
  • FIG. 1 illustrates a typical gown 100 to be worn during a medical procedure as seen from the front. The gown 100 includes a collar 110, the cuffs 120, the primary tie cord 130 and a primary tie cord attachment area 140. The shoulder seams 150 linking the sleeves 160 to the main body 170 are also visible. FIG. 2 illustrates a typical gown 100 to be worn during a medical procedure as seen from the back. In FIG. 2 the shoulder seams 150 linking the sleeves 160 the main body 170 are visible as are the sleeve seams 180 running from the shoulder seams 150 to the cuffs 120 which are used to produce the sleeves 160. FIG. 2 also shows a secondary tie cord 180 and secondary tie attachment area 190 (not in the AAMI critical zone). FIG. 3 represents the tie cord 130 and shows the end to be bonded to the gown 100 as having, in this case, a “Y” shaped end 200 for attachment to the gown 100. Note that a simple flat shaped end may also be used for attachment to the gown, a “Y” shape is not required.
  • Many surgical gowns are made from thermally sensitive laminate barrier materials composed of thermoplastic polymers. While such barrier materials may be in the form of thermoplastic polymer spunbond fabrics, thermoplastic polymer meltblown fabrics, and various combinations of such spunbond and meltblown fabrics, a particularly desirable form of these barrier materials incorporate one or more thin, breathable films that provide desirable levels of resistance to penetration by liquids and pathogens while also providing satisfactory levels of breathability and/or moisture vapor transmission.
  • These thin and breathable films are commonly made from thermoplastic polyolefins like polyethylene and polypropylene and copolymers thereof because of their relatively low cost and ability to be processed. Polyethylene is generally used in the film production and the film is commonly “filled” with calcium carbonate, various kinds of clay, silica, alumina, barium carbonate, soldium carbonate, magnesium carbonate, talc, barium sulfate, magnesium sulfate, aluminum sulfate, titanium dioxide, zeolites, cellulose-type powders, kaolin, mica, carbon, calcium oxide, magnesium oxide, aluminum hydroxide, pulp powder, wood powder, cellulose derivatives, chitin and chitin derivatives, to increase breathability. Fillers produce microscopic pores in the film upon stretching to increase porosity. Unfortunately, these thin and breathable films are considered to be thermally sensitive because they have a tendency to become compromised by heat and/or or pressure. When these films are incorporated into laminate barrier materials by sandwiching them together with various combinations of other materials such as, for example, spunbond fabrics, meltblown fabrics and combinations thereof, the resulting laminate barrier materials are generally considered to be thermally sensitive as well. This characterization is particularly important for post-laminate formation processing steps. That is, manufacturing operations that convert the thermally sensitive barrier fabrics after such films are formed into the laminate barrier fabrics. For example, when thermally sensitive barrier materials are converted into gowns or other articles utilizing thermal point bonding and/or ultrasonic bonding techniques or when components such as, for example, tie cords or other features are attached to the articles, the breathable films of barrier laminate are frequently compromised such that they so longer provide desired levels of barrier to liquid penetration and pathogens.
  • The thin and breathable film laminates described above may be thermally bonded using bar sealing, thus producing a thermal bond for a film layer-containing thermoplastic fabric where the bond joins a thermoplastic material to the fabric to form a fused bonded area, without bonding to the film layer. This bond has no un-melted areas remaining within the fused bond area on the surface.
  • “Spunbond” refers to fabric made from small diameter fibers which are formed by extruding molten thermoplastic material as filaments from a plurality of fine, usually circular capillaries of a spinneret with the diameter of the extruded filaments then being rapidly reduced as by, for example, in U.S. Pat. No. 4,340,563 to Appel et al., and U.S. Pat. No. 3,692,618 to Dorschner et al., U.S. Pat. No. 3,802,817 to Matsuki et al., U.S. Pat. Nos. 3,338,992 and 3,341,394 to Kinney, U.S. Pat. No. 3,502,763 to Hartman, and U.S. Pat. No. 3,542,615 to Dobo et al. Spunbond fibers are generally not tacky when they are deposited onto a collecting surface. Spunbond fibers are generally continuous and have average diameters (from a sample of at least 10) larger than 7 microns, more particularly, between about 10 and 20 microns.
  • “Meltblown” fabric is formed by extruding a molten thermoplastic material through a plurality of fine, usually circular, die capillaries as molten threads or is filaments into converging high velocity, usually hot, gas (e.g. air) streams which attenuate the filaments of molten thermoplastic material to reduce their diameter, which may be to microfiber diameter. The meltblown fibers are then carried by the high velocity gas stream and are deposited on a collecting surface to form a web of randomly dispersed meltblown fibers. Such a process is disclosed, for example, in U.S. Pat. No. 3,849,241 to Butin et al. Meltblown fibers are microfibers which may be continuous or discontinuous, are generally smaller than 10 microns in average diameter, and are generally tacky when deposited onto a collecting surface.
  • Laminates of spunbond and meltblown fabrics, e.g., spunbond/meltblown/spunbond (SMS) laminates and others are disclosed in U.S. Pat. No. 4,041,203 to Brock et al., U.S. Pat. No. 5,169,706 to Collier, et al, U.S. Pat. No. 5,145,727 to Potts et al., U.S. Pat. No. 5,178,931 to Perkins et al. and U.S. Pat. No. 5,188,885 to Timmons et al. Such a laminate may be made by sequentially depositing onto a moving forming belt first a spunbond fabric layer, then a meltblown fabric layer and last another spunbond layer and then bonding the laminate in a manner described below. Alternatively, the fabric layers may be made individually, collected in rolls, and combined in a separate bonding step. Such fabrics usually have a basis weight of from about 0.1 to 12 osy (6 to 400 gsm), or more particularly from about 0.75 to about 3 osy. Multilayer laminates may also have various numbers of meltblown layers or multiple spunbond layers in many different configurations and may include other materials like films (F) or coform materials, e.g. SMMS, SM, SFS, etc.
  • An exemplary method of forming a film includes a co-extrusion film apparatus that forms the film with multiple layers consisting of skin and core layers. Typically the apparatus will include two or more polymer extruders. In one method of fabrication, the film is extruded into a pair of nip or chill rollers. In another method the film is extruded onto a chilled roll which can have a smooth or matte finish. Typically, the film as initially formed will have an overall thickness of approximately 25 to 60 micrometers with, in the case of multilayer films, the total skin or bonding layer having an initial thickness that may be about 3% to 30% of the total thickness. Other film making processes known to those skilled in the art may be used as well, including cast embossing, chill and flat casting and blown film processes.
  • From the coextrusion film apparatus the film is directed to a film stretching unit such as a machine direction orienter (MDO), which is a commercially available device from vendors such as the Marshall and Williams Company of Providence, R.I. Such an apparatus has a plurality of paired stretch rolls that move at predetermined speeds that may rotate faster, slower or at the same speed relative to each other. Typically the stretch rolls move at a progressively faster speeds to progressively stretch and thin the film in the machine direction of the film, which is the direction of travel of the film through the process. The stretch rolls are generally heated for processing advantages.
  • The temperatures to which the film is heated while stretching will depend on the composition of the film as well as the breathability and other desired end properties of the laminate. In most cases the film will be heated to a temperature no higher than 5 degrees ° C. below the melting point of the core or “B” layer in the film. The purpose for heating the film is to allow it to be stretched quickly without causing film defects. The amount of stretching will depend on the polymeric composition, but, in general, the film may be stretched to about 300% or more of its original length (that is, a one cm length, for example, will be stretched to 3 cm) but less than the amount that tends to result in film defects. For most applications, for example, the stretch will be to at least 200% of the original film length and, frequently, in the range of about 250% to 500%.
  • The multilayer stretch-thinned film may be attached to one or more support layers to form a multilayer film/nonwoven laminate as described above. For example, a conventional fibrous nonwoven web forming apparatus, such as a pair of spunbond machines, may be used to form the support layer. The long, essentially continuous fibers are deposited onto a forming wire as an unbonded web and the unbonded web is then sent through a pair of bonding rolls to bond the fibers together and increase the tear strength of the resultant web support layer. One or both of the rolls are often heated to aid in bonding. Typically, one of the rolls is also patterned so as to impart a discrete bond pattern with a prescribed bond surface area to the web. The other roll is usually a smooth anvil roll but this roll also may be patterned if so desired.
  • Once the multilayer film has been sufficiently thinned and oriented and the support layer has been formed, the two layers are brought together and laminated to one another using a pair laminating rolls or other means. As with the bonding rolls, the laminating rolls may be heated. Also, at least one of the rolls may be patterned to create a discrete bond pattern with a prescribed bond surface area for the resultant laminate. Generally, the maximum bond point surface area for a given area of surface on one side of the laminate will not exceed about 50 percent of the total surface area.
  • The process described above may be used to create a three layer laminate. The only modification to the previously described process is to feed a supply of a second fibrous nonwoven web support layer into the laminating roll on a side of the multilayer film opposite that of the other fibrous nonwoven web support layer. Alternatively, as with the other layers, the support layer may be formed directly in-line. In either event, the second support layer is fed into the laminating rolls and is laminated to the multilayer film in the same fashion as the other support layer.
  • Exemplary processes and materials for forming thin films and laminates may be found in commonly assigned U.S. Pat. Nos. 5,188,885, 5,213,881, 5,271,883, 5,464,688, 5,695,868, 6,037,281, 6,309,736, 6,653,523 and 6,764,566, incorporated herein in their entirety.
  • Multilayer film laminates may have various numbers of meltblown layers or multiple spunbond layers in many different configurations and may include other materials like coform materials. These include, for example, spunbond/film/spunbond (SFS) laminates, spunbond/film/meltblown (SFM) laminates, spunbond/meltblown/film (SMF) laminates and laminates having a greater number of layers like spunbond/film/spunbond/meltblown/spunbond (SFSMS) and spunbond/meltblown/film/meltblown/spunbond SMFMS, coform/meltblown/film (CMF) etc.
  • As used herein, the term “thermally sensitive materials” means fabrics and webs which have a tendency to become compromised by heat and/or or pressure. These materials have a relatively narrow range of temperature (the bonding window) at which they can be bonded and can be damaged to a great degree when conditions fall outside of these ranges.
  • A “substantially solid bond” is one in which there are no substantially un-melted areas within the bond footprint. This means that the thermoplastic fibers on the surface have been melted to a degree sufficient to produce a film. The surface film thus produced is the material which results in a bonding together of the two layers that are desired to be bonded.
  • Previous tie cord sealing methods tended to damage the layers of the gown and to impair the liquid resistance of the bond to a point that the gown failed the MMI level 4 test at the bond, or to be prohibitively expensive. These methods included ultrasonic or thermal point bonding and adhesive bonding. The inventors believe, though do not wish to bound by that belief, that the former methods tend to bond materials through their entire thickness, thus disrupting the structure to a relatively high degree. Since many surgical gowns include a film layer in order to increase the penetration resistance of the gown and because film layers tend to be relatively weak, the robust bonding used previously tended to damage this layer and increase liquid penetration. In the case of adhesive bonding the manufacturing challenges and expense are relatively great since adhesives tend to be expensive and time consuming to apply and can have detrimental effects on manufacturing facility cleanliness. The inventors believe, though do not wish to bound by that belief, that bar sealing can bond a thermoplastic material to a second thermoplastic material that has a film layer within it, without damaging the barrier properties of the film layer. Bar sealing is also substantially less expensive and less challenging in a manufacturing environment than is adhesive bonding.
  • Bar sealing uses heat, pressure and dwell time to thermally bond thermoplastic materials together. According to the present invention, these variables are adjusted so that the thermal bonding takes place substantially at or adjacent the surface of the thermally sensitive barrier laminate materials while avoiding degradation of the thermally sensitive film component in an interior region of the barrier laminate.
  • Bar sealing devices generally have a press with a set of jaws that open (vertically), into which the materials to be bonded are placed. The jaws are heated by, for example, electric resistance heating and the temperature of each may be controlled separately. The pressure at which the jaws come together may also be adjusted for optimal bonding. Lastly, the time for which the jaws are together (the “dwell” or “hover” time) may also be adjusted. A dwell time of zero indicates that the jaws were brought together for an instant and immediately moved apart, i.e., they were not held together.
  • Different applications may require different jaw sizes, but the size of jaw is generally about a 1.75 cm (a half inch) wide, producing a bond width of about 0.635 cm (¼ inch), by about 3.8 cm long (1.5 inches) to about 6.35 cm (2.5 inches) long. The jaw size may be as small as a half centimeter by a centimeter, depending on the materials to be joined.
  • An exemplary bar sealing device is available from Therm-O-Seal® Corporation of Mansfield, Tex. One such device is a Vertrod® Style Steel frame sealer that has jaws about 1.75 cm wide and 2.54 cm in length and uses electrical resistance heating and water cooling. Another is a Vertrod® style hand-held heat sealer that can produce a bond of 2, 4, 8 or 12 inches (5.1, 10.16, 20.3 and 30.5 cm) in length and ⅛, 3/16, ¼ and ⅜ inch (0.32, 0.48, 0.64 and 0.95 cm) in width. Yet another example of a bar sealing device is a Vertrod® style table-top vacuum heat sealer producing seals 9, 14, 20, 24 and 30 inches (22.9, 35.6, 50.8, 61 and 76.2 cm) in length and ⅛, 3/16, ¼ and ⅜ inch in width.
  • As noted above, the process conditions will vary depending on the materials of construction. For example, the current thermoplastic polymeric materials commonly used in disposable gowns and for components such as, for example, tie cords that are presently attached to such disposable gowns, are typically nonwoven fabrics formed from polypropylene and/or polyethylene and have a basis weight typically ranging from about 0.5 (17 gsm) to about 1.5 osy (51 gsm).
  • Desirably, the tie cord material may be a folded 1.0 osy (34 gsm) SMS material made as described above. Fabric for the fabrication of gowns may be, for example, made of random copolymer spunbond, a three layer (Catalloy®/polyethylene/Catalloy®) or “ABA” calcium carbonate filled film, and a spunbond/meltblown/spunbond (SMS) layer. This “SFSMS” may bonded together to form the gown with the SMS against the skin. The spunbond layer and film may have a basis weight of between 0.2 and 1.0 osy (7 and 34 gsm) or more particularly about 0.6 osy (20.3 gsm). The SMS layer may have a basis weight of between 0.5 and 1.5 osy (17 and 51 gsm) or more particularly about 0.75 osy (25.4 gsm).
  • When these materials are used, the temperature of the bar sealer should be between 240 and 320° F. (116 and 160° C.), the pressure should be between 40 and 80 psi (276 and 552 kPa) and the dwell time should be between 0 and 5 seconds. More particularly, the temperature should be between 260 and 290° F. (127 and 143° C.), the pressure should be between 50 and 60 psi (345 and 414 kPa) and the dwell time should be between 1 and 3 seconds.
  • Test Methods ASTM tests 1670 and 1671-b, procedure A: These tests are identical except that 1670 uses synthetic blood and 1671 uses Phi-X174 bacteriophage.
  • The test uses a penetration test cell available from Wilson Road Machine Shop, Rising Sun, Md. The cell has a capacity of about 60 ml. In the test cell, the specimen acts as a partition separating the challenge fluid from the viewing side of the penetration cell. An annular flange cover with an open area to allow visual observations of the specimen, and a transparent cover are included. The cell body has top port for filling and a drain valve for draining the penetration test cell. The penetration cell is further specified in Test Method F903.
  • The fabric specimen is placed in the penetration cell with the layer that is normally outermost facing the back (solid flange) part of the cell where the challenge fluid is placed. The cell is filled through the top port with the challenge fluid and observed for 5 minutes. Air is then supplied to the top port and the sample held at 13.8 kPa (2 psig) for 1 minute and the pressure released. If liquid penetration is not yet seen, the sample is allowed to stand for 54 minutes and observed. If bacteriophage is the test fluid, the sample is subsequently assayed using a 0.5 ml sample size onto agar for 6 to 18 hours at 35 to 37° C. to test for passage of fluid that is not observable to the unaided eye.
  • EXAMPLES
  • Kimberly-Clark MicroCool® surgical gowns are made of random copolymer spunbond, a three layer (Catalloy®/polyethylene/Catalloy®) calcium carbonate filled film, and a spunbond/meltblown/spunbond (SMS) layer. This “SFSMS” is bonded together to form the gown with the SMS against the skin. The random copolymer of which the outermost layer of spunbond material is made is a 2.5 weight percent ethylene-propylene copolymer known as R532-35R, from the Dow Chemical Company of Midland, Ml. No treatments are applied to the fabric.
  • The spunbond layer and film each had a basis weight of 0.6 osy (20.3 gsm). The SMS layer had a basis weight of 0.75 osy (25.4 gsm).
  • The tie cord to be bonded to the gown was a folded 1.0 osy (34 gsm) SMS material. The material was folded either once for a double layer of fabric, or twice for a triple layer of fabric. The outer layer (spunbond) was made from a 2.5 weight percent ethylene-propylene copolymer known as R532-35R, from the Dow Chemical Company and the outer layer is treated with an antistat and a fluorochemical to reduce surface tension. Prior to bonding to the gown, a additional piece of tie cord material was bonded to the tie cord near an end to produce a “Y” shaped end for bonding to the gown on both upper end of the Y. The Y was flattened out onto the gown for bonding at two points on the branches of the Y but near the stem of the Y.
  • A bar sealing device from Therm-O-Seal® of Mansfield, Tex. was used. It was a Vertrod® model number 2PF-ST-12004-55HT-WC-CRF-TC-KY-SP. This device had jaws about 1.75 cm wide and 2.54 cm in length and used electrical resistance heating and water cooling. Only the jaw in contact with the tie cord was heated.
  • Example 1
  • A double folded SMS tie cord was bonded to a MicroCool® surgical gown at a temperature of 275 to 282° F. (135 to 139° C.) at a zero dwell time and 56 psi pressure (386 kPa). The bonded area was tested according to ASTM 1670. Nine out of 11 samples passed and two failed.
  • Example 2
  • A double folded SMS tie cord was bonded to a MicroCool® surgical gown at a temperature of 280 to 286° F. (138 to 141° C.) at a zero dwell time and 56 psi pressure (386 kPa). The bonded area was tested according to ASTM 1670. All 11 samples passed
  • Example 3
  • A double folded SMS tie cord was bonded to a MicroCool® surgical gown at a temperature of 290 to 296° F. (143 to 147° C.) at a zero dwell time and 56 psi pressure (386 kPa). The bonded area was tested according to ASTM 1670. Nine out of 11 samples passed and two failed.
  • Example 4
  • The samples from Example 2 were tested according to ASTM 1671-b using bacteriophage. Eleven of 11 samples passed.
  • As will be appreciated by those skilled in the art, changes and variations to the invention are considered to be within the ability of those skilled in the art. Examples of such changes are contained in the patents identified above, each of which is incorporated herein by reference in its entirety to the extent it is consistent with this specification. Such changes and variations are intended by the inventors to be within the scope of the invention. It is also to be understood that the scope of the present invention is not to be interpreted as limited to the specific embodiments disclosed herein, but only in accordance with the appended claims when read in light of the foregoing disclosure.

Claims (20)

1. A surgical gown having an AAMI critical zone comprising a tie cord bar sealed to said gown at a bond in said critical zone wherein said bond passes AAMI level 4 testing.
2. The gown of claim 1 wherein said bond is made at a temperature between 240 and 320° F. (116 and 160° C.), a pressure between 40 and 80 psi (276 and 552 kPa) and a dwell time between 0 and 5 seconds.
3. The gown of claim 1 wherein said bond is made at a temperature between 260 and 290° F. (127 and 143° C.), a pressure between 50 and 60 psi (345 and 414 kPa) and a dwell time between 1 and 3 seconds.
4. The gown of claim 1 wherein said gown comprises a polyolefin microfiber layer.
5. The gown of claim 4 wherein said gown further comprises a filled film.
6. A surgical gown having a tie cord and a tie cord bond area where said tie cord is bonded to said gown, wherein said tie cord bond area passes ASTM test 1671-b.
7. A thermal bond for a film layer-containing thermoplastic fabric wherein said bond joins a thermoplastic material to said fabric to form a fused bonded area, without bonding to said film layer.
8. The bond of claim 7 wherein no un-melted areas remain within the fused bond area on the surface.
9. The bond of claim 7 wherein said film layer-containing thermoplastic fabric further comprises a filler within said film layer.
10. The bond of claim 7 wherein said thermal bond is produced substantially at or adjacent a surface of the film layer-containing thermoplastic fabric while avoiding degradation of said film layer in an interior region of said fabric.
11. The bond of claim 7 wherein said thermal bond has a width of between 0.32 and 1.75 cm.
12. The bond of claim 11 wherein said thermal bond has a length of between 2.54 and 76 cm.
13. The bond of claim 7 wherein said film layer-containing thermoplastic fabric is a spunbond/film laminate.
14. The bond of claim 13 wherein said spunbond layer is made from polyethylene, polypropylene or an ethylene-propylene copolymer.
15. The bond of claim 13 wherein said film layer is a stretch-thinned film.
16. The bond of claim 15 wherein said film layer further comprises calcium carbonate.
17. The bond of claim 15 wherein said film is a an ABA film.
18. The bond of claim 17 wherein said film is heated to a temperature no higher than 5 degrees ° C. below the melting point of the B layer in the film.
19. The bond of claim 18 wherein said film is stretched to about 250% to 500% of its unstretched length.
20. The bond of claim 18 wherein said film is stretched to about 300% of its unstretched length.
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US20080155728A1 (en) * 2006-12-28 2008-07-03 Greg Hafer Surgical gown tie attachment
US20100313326A1 (en) * 2009-06-11 2010-12-16 Craig Turner Outer garment
WO2011060003A1 (en) * 2009-11-11 2011-05-19 Null Warren J Cast and iv medical shower system

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MX2009001211A (en) 2009-02-13
WO2008026090A1 (en) 2008-03-06

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