US2364692A - Textile printing emulsions - Google Patents

Textile printing emulsions Download PDF

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US2364692A
US2364692A US351206A US35120640A US2364692A US 2364692 A US2364692 A US 2364692A US 351206 A US351206 A US 351206A US 35120640 A US35120640 A US 35120640A US 2364692 A US2364692 A US 2364692A
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lacquer
resin
emulsion
water
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Norman S Cassel
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Interchemical Corp
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/44General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders

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  • This invention relates to pigmented lacquer emulsions useful in the decoration of fabrics, and has particular reference to composite emulsions containing a plurality of dispersed phases.
  • lacquers have also been generally unacceptable due to the fact that the fabricsprinted with lacquers develop an undesirable stifl. feel (known to the trade as hand") to the necessity for using large amounts of color to obtain deep shades, and to the tendency of colored markings to rub off onto other clothing and leave. a mark (known as crocking).
  • lacquers for dyeing has also been attempted, and has failed for the same reasons, and for the additional reason that pigments tend to fiocculate and settle out in the very thin lacquers useful for penetrating cloth.
  • the binder-of the lacquer is one which is originally soluble in ordinary orgame solvents and which can be converted into an insoluble state after printing-most desirably, a readily heat-polymerizable synthetic resin, best exemplified by plastlclzed urea-formaldehyde type resins.
  • a readily heat-polymerizable synthetic resin best exemplified by plastlclzed urea-formaldehyde type resins.
  • Emulsions of pigmented lacquers containing similar binders have also been suggested for the p gment dyeing of textile fabrics and have met with some success; but the problem of, pigment d stribution in such dye baths has been a major d fficulty. Very often only a small amount of plem nt is wanted in a dilute lacquer phase; and settling and aggregation of pigment makes the problem of uniform coloration unusually difilcult.
  • My means comprises the use of multiple phase emulsions in which water is one phase, a concentrated pigmented resin-solvent aggregate is another phase, and a lacquer of very low solids content, which is only partially miscible with the pigmented resin-solvent lacquer from which the aggregate is formed, is the third phase.
  • the pigmented resin-solvent aggregate phase is made by dispersing pigment in a rather concentrated solution of a binder com rising a. heatconvertible sy thetic resin, so this; the pigment will remain dispersed in the At least two volumes of binder to one of pigment should be used, since at least this much binder is required to hold the pigment tightly to the resultant lacquer,
  • the resin solution not be one capable of infinitely diluting the resin solution; preferably, it is one which will produce some precipitation of the resin on substantial reduction of resin content.
  • the low solids lacquer should preferably contain a maximum of non-volatile, particularly where economy and reduced hand are desirable, and most preferably the non-volatile content should be as low as possible consonant with the production of a stable emulsion, the non-volatile solute of this lacquer acting essentially as an emulsifying agent for the water employed.
  • the important function of this lacquer is contributed by the solvent. It must be capable of diluting the pigmented lacquer phase when added in small quantities, but should cause cloudiness when added in larger quantities.
  • Any heat-convertible resin may be used provided solvents are available with the desired properties.
  • urea-formaldehyde resin including resins made from its homologues and derivatives, such as thiourea, cyanuric acid, biuret, melamine, etc.
  • the soluble heat-convertible alkyd resins such as thiourea, cyanuric acid, biuret, melamine, etc.
  • heat-convertible phenolic resins and the like.
  • the solvents used will vary depending on the resin.
  • the original solvent may be a mixture of an alcohol and an aromatic hydrocarbon, with some terpenes if desired;
  • the diluting solvent added in the low-solids lacquer may be aliphatic or aromatic hydrocarbons, or a mixture of aliphatic and aromatic hydrocarbons.
  • aliphatic hydrocarbons may be used as the diluent; those alkyds containing sufficient fatty acids to be soluble in aliphatic hydrocarbons are beyond the ready heat-convertible state, and cannot be used alone.
  • my invention When my invention is used in the water-inlacquer emulsion printing pastes, it permits the dilution of the color to the desired shade with a very low-solids diluent lacquer, without danger of causing aggregation of the pigment.
  • the pigment remains protected by the same amount of resin, and thus is as resistant to washing and rubbing. Furthermore, the pigment-resin aggregate is deposited in far more discontinuous islands than in the concentrated form, while the diluting lacquer deposits little solids; as a result, the hand" of the fabric is kept at a minimum.
  • Typical examples of my invention are the following:
  • Alkyd resin printing paste A lacquer is made by mixing Parts by weight Alkyd resin solution-50% in toluene 20 Pine oil 8 Solvesso #3 (hydrogenated petroleum solvent-boiling range 175-210 C.) 28
  • Solvesso #3 1.20 A 15% rubber solution in Solvesso #2 (hydrogenated petroleum solvent-boiling range -177 C.) 1.00 Solvesso #2 22.00
  • the alkyd resin is a 40% drying oil modified glycerol phthalate resin, which is freely soluble in hydrogenated petroleum solvents, as distinguished from the alkyd resin of Example 1.
  • This unpigmented emulsion contains 0.75% solids; the lacquer phase contains about 3% solids. It may be blended with the pigmented emulsion of Example 1 (13.2% solids-lacquer phase about 18% solids) in ratios of 1 to 1 and higher, to produce a three-phase system in which a low-solids clear lacquer the outer phase, and water and resin-solvent aggregate bearing pigment are the inner phases. Microscopic examination of the mixture indicates that the two disperse phases are in very close contact with one another. The mixtures are stable, and prints made therewith show the same resistance to washing and other influences as prints made from Example 1.
  • Urea-formaldehyde alkyd paste A typical water-in-lacquer printing emulsion may be made as in Example 1 fromlacquer phase Parts by weight Urea resin solution of Example 3 5.0 Alkyd resin solution of Example 1 15.0 Pine oil 5.0 Solvesso 34.0 20% pulp phthalocyanine green 30.0 Water 11.0
  • the lacquer is then emulsified into Parts by weight Water 46.0 Sodium lauryl sulfate 2.0 Dry bent ni 3.0
  • Example 1 Made as in Example 1; it may be reduced with the unpigmented emulsions of Examples 2and4. All of the above examples may be made by first mixing the pigmented lacquers with the clear lacquers of Examples 2 and 4, provided water is immediately emulsified therein; or the clear lacquers of'Examples 2 and 4 maybe added to the emulsions with These methods, however, lack flexibility, since the pigmented emulsion and the diluting emulsion may both be made of printing consistency, so they can be mixed in any desired'proportions before use.
  • the pigment may be added in pulp form as indicated. or it may be dispersed in conventional fashion.
  • lacquer-in-water emulsions may be used.
  • Pigment dyeing emulsions Carbon black are dispersed in- Alkyd resin solution. (65 parts" alkyd resin of Example 1, 35' parts xylene) 10.0
  • An excellent pigment dyeing bath is made from 1 part of the pigmented emulsion and 4 or more parts of the unpigmented material.
  • the same effect may be obtained by adding water to the pigmented emulsion, then adding the emulsifying agent to the water, and then adding the solvent.
  • the diluting solvent contain some emulsifying agent therein so that it may form a stable emulsion; and where high non-volatile (solids) content is undesirable, the solids ofthe diluting low-solids lacquer phase should not exceed about by weight of that phase.
  • oLaqueous phase needed to prevent separation of the two lacquer phases varies of course with the degree of incompatibility; but in general, of aqueous phase, based on the complete emulsion, is sufiicient. For reasons of economy, and for better working properties, higher amounts are preferable, as indi-' cated in the examples.
  • aggregate as used to describe the pigmented resin-solvent aggregate phase, is used in its popular sense, and not in any technical sense.
  • An emulsion comprising an aqueous phase, a phase consisting essentially of a volatile waterimmiscible organic liquid having dissolved therein less than 10% of non-volatile, including an 40 agent capable of producing a stable emulsion of water and said liquid, and adispersed phase of pigmented resin-solvent aggregate derived from a heat-convertible resin lacquer which is miscible with limited quantities of said organic liquid, but immiscible with the quantities employed in the emulsion.
  • a textile decorating emulsion comprising a discontinuous aqueous phase comprising at least 20% by weight of the emulsion, a continuous phase consisting essentially of a volatile waterimmiscible organic liquid having dissolved therein an agent capable of producing a stable emulsion of water and said liquid, and a dispersed phase of pigmented resin-solvent aggregate derived from a pigmented heat-convertible resin lacquer which is miscible with limited quantities of of said organic liquid, but immiscible with the quantities employed in the emulsion.
  • a textile decorating emulsion comprising a discontinuous aqueous phase comprising at least 20% by weight of the emulsion, a continuous phase consisting essentially of a volatile waterimmiscible organic liquid having dissolved therein less than 10% of non-volatile, including an agent capable of producing a stable emulsion of water and said liquid, and a dispersed phase of pigmented resin-solvent aggregate derived from a pigmented heat-convertible resin lacquer which is miscible with limited quantities of said organic liquid but immiscible with the quantities employed in the emulsion.
  • composition of claim 2 in which the heat-convertible resin comprises a heat-convertible alkyd resin.
  • composition of claim 2 in which the heat-convertible resin comprises a plasticized urea formaldehyde resin.
  • a textile coloring emulsion comprising an outer continuous aqueous phase and two organic phases, one of which consists essentially of a volatile water-immiscible organic liquid having dissolved therein less than 10% of non-volatile, including an agent capable of producing a stable emulsion of water and said liquid, and the other of which consists of pigmented resin-solvent aggregate derived from a, heat-convertible resin lacquer which is miscible with limited quantities of said organic liquid, but immiscible with the quantities employed in the emulsion.
  • the method of producing a textile decorating emulsion which comprises preparing a waterin-lacquer emulsion, the outer phase of which is pigment dispersed in a lacquer, the binder of which comprises a heat-convertible synthetic resin, the lacquer being of such body that pig'- ment will remain dispersed in it, separately preparing a second water-in-lacquer emulsion, the outer phase of which is a lacquer consisting essentially of volatile solvent having dissolved therein an agent which renders the lacquer capable ofemulsifying water therein, the second lacquer being only partially miscible with the first lacquer, and having a substantially lower nonvolatile content than the first lacquer, and mixing the emulsions to produce an emulsion in which the outer phase consists essentially of the second lacquer, and the inner phases of which comprises water and the first lacquer.

Description

Patented Dec. 12, 1944 TEXTILE PRINTING EMULSIONS Norman S. Cassel, Ridgewood, N. J., assignor to Inter-chemical Corporation, New York, N. Y., a
corporation of Ohio Serial No. 351,206
No Drawing. Application August 3, 1940,
7 Claims. (Cl. 260-29) This invention relates to pigmented lacquer emulsions useful in the decoration of fabrics, and has particular reference to composite emulsions containing a plurality of dispersed phases.
The printing and dyeing of textile fabrics has been done for ages with soluble colors which are applied in solution, and fixed in or to the fibers by chemical action. Conventional textile printing is ordinarily done with water solutions of dyestuffs containing water soluble thickening agents in sufiicient quantity to retard the spreading of the color on the fabric after printing. The dyestuff is fixed onto the fabric by some chemical process, and the binding agent is then washed out of the fabric. The time and expense involved in this after treatment, added to the originally high color cost for light and tub fast dyes, has been a major problem in textile printing. An unsolved problem has been the reproduction of 7 very fine designs. Since the pastes spread on the fabric after printing when thin enough to be removed sharply from fine engravings, giving blurred designs, it has been found impossible to use photogravure cylinders or extremely fine mill and dye engravings. Attempts to modify these pastes by addition of wetting agents and emulsification of oils :therein have not solved the basic difficulties.
The use as printing pastes of ordinary colored lacquers (which, for the purpose of this application are defined as dispersion of color in vehicles consisting of a solution of plastic or solid film forming, water resistant binder such as a cellulose derivative or resin, in an organic solvent or mixture of solvents) has been attempted in order to overcome the difiiculties with prior art pastes,
but has not been successful commercially. Relatively few lacquer compositions withstand both dry cleaning and washing; and lacquers have also been generally unacceptable due to the fact that the fabricsprinted with lacquers develop an undesirable stifl. feel (known to the trade as hand") to the necessity for using large amounts of color to obtain deep shades, and to the tendency of colored markings to rub off onto other clothing and leave. a mark (known as crocking). The use of lacquers for dyeing has also been attempted, and has failed for the same reasons, and for the additional reason that pigments tend to fiocculate and settle out in the very thin lacquers useful for penetrating cloth.
There has recentlyvbeen developed a new type of textile printing paste which eliminates the disadvantages of the conventional dye printing pastes and avoids the difiiculties which have been pastes. These new pastes are emulsions in which encountered in the prior art lacquer printing an outer continuous, water-immiscible-lac uer phase is thickened by an inner aqueous p ase which is at least'20 per cent. of the total emulsion, by weight. Preferably, the binder-of the lacquer is one which is originally soluble in ordinary orgame solvents and which can be converted into an insoluble state after printing-most desirably, a readily heat-polymerizable synthetic resin, best exemplified by plastlclzed urea-formaldehyde type resins. The use of pastes made in accordance with this invention permits of the use of cheap pigments and avoids the after treatment necessary with conventional printing pastes. Furthermore, these new pastes separate sharply even from very fine photogravm-e cylinders, although thickened sufflciently to prevent any spreading on the fabric; this makes possible much finer printing than can be obtained with conventional pastes. The hand imparted to fabrics by these new pastes is very much less than the hand imparted to similar fabriosby ordinary lacquer pastes having the same binder, the amount of color needed to produce deep shades is sharply reduced, and the crockmg substantially eliminated.
Emulsions of pigmented lacquers containing similar binders have also been suggested for the p gment dyeing of textile fabrics and have met with some success; but the problem of, pigment d stribution in such dye baths has been a major d fficulty. Very often only a small amount of plem nt is wanted in a dilute lacquer phase; and settling and aggregation of pigment makes the problem of uniform coloration unusually difilcult.
I have invented a means of overcoming'the problem of pigment distribution in dilute pigmented lacquer dye baths, and further improvmg the properties of water-in-lacquer emulsion prmtmg pastes. My means comprises the use of multiple phase emulsions in which water is one phase, a concentrated pigmented resin-solvent aggregate is another phase, and a lacquer of very low solids content, which is only partially miscible with the pigmented resin-solvent lacquer from which the aggregate is formed, is the third phase. The pigmented resin-solvent aggregate phase is made by dispersing pigment in a rather concentrated solution of a binder com rising a. heatconvertible sy thetic resin, so this; the pigment will remain dispersed in the At least two volumes of binder to one of pigment should be used, since at least this much binder is required to hold the pigment tightly to the resultant lacquer,
not be one capable of infinitely diluting the resin solution; preferably, it is one which will produce some precipitation of the resin on substantial reduction of resin content.
The low solids lacquer should preferably contain a maximum of non-volatile, particularly where economy and reduced hand are desirable, and most preferably the non-volatile content should be as low as possible consonant with the production of a stable emulsion, the non-volatile solute of this lacquer acting essentially as an emulsifying agent for the water employed. The important function of this lacquer is contributed by the solvent. It must be capable of diluting the pigmented lacquer phase when added in small quantities, but should cause cloudiness when added in larger quantities. This results in the formation of a dispersed phase of pigmented resin-solvent aggregate in the low solids lacquer; flocculation of the pigment with insufiicient resin to protect it is prevented since the pigment is held tightly to the dispersed resinsolvent ag regate.
These dispersions of the pigmented resin-solvent aggregate in thin lacquer settle out very rapidly, and often are not easily redispersible; the function of the water in the emulsion is to prevent such a settling out, and to preserve the desired structure. Therefore,,whi1e the two lacquer phases can be mixed, and water then emulsified, I prefer to emulsify at least one phase, and preferably both, with water before mixing them.
Any heat-convertible resin may be used provided solvents are available with the desired properties. I have successfully used urea-formaldehyde resin (including resins made from its homologues and derivatives, such as thiourea, cyanuric acid, biuret, melamine, etc.), the soluble heat-convertible alkyd resins (those modified with low percentages of fatty acids), heat-convertible phenolic resins, and the like.
The solvents used will vary depending on the resin. Thus, with urea and the shorter oii alkyd resins, the original solvent may be a mixture of an alcohol and an aromatic hydrocarbon, with some terpenes if desired; the diluting solvent added in the low-solids lacquer may be aliphatic or aromatic hydrocarbons, or a mixture of aliphatic and aromatic hydrocarbons. With longer oil alkyds which are soluble in aromatic hydrocarbons, aliphatic hydrocarbons may be used as the diluent; those alkyds containing sufficient fatty acids to be soluble in aliphatic hydrocarbons are beyond the ready heat-convertible state, and cannot be used alone. With phenolic resins, alcohols may be used as the original solvents, various hydrocarbons as diluents. It should be observed that the tendency toward immiscibility is always increased by the incorporation of pigment into the resin lacquer; this should always be considered.
When my invention is used in the water-inlacquer emulsion printing pastes, it permits the dilution of the color to the desired shade with a very low-solids diluent lacquer, without danger of causing aggregation of the pigment. The pigment remains protected by the same amount of resin, and thus is as resistant to washing and rubbing. Furthermore, the pigment-resin aggregate is deposited in far more discontinuous islands than in the concentrated form, while the diluting lacquer deposits little solids; as a result, the hand" of the fabric is kept at a minimum.
In dyeing operations, where the fabric is impregnated throughout, reduction of resin deposited is even more important; and my method permits of efiective pigment dyeing with an absolute minimum of resin deposition, while maintaining uniformity of pigment distributions.
Typical examples of my invention are the following:
- EXAMPLE 1 Alkyd resin printing paste A lacquer is made by mixing Parts by weight Alkyd resin solution-50% in toluene 20 Pine oil 8 Solvesso #3 (hydrogenated petroleum solvent-boiling range 175-210 C.) 28
Into this lacquer is emulsified Parts by weight A Ni /2% aqueous pulp of LithosolBlue G. L 20 Water Y 24 EXAMPLE 2 Reducing emulsionwater-in-lacquer A lacquer is made by mixing- Parts by weight A solution of 50 alkyd resin; 15 pine oil; 35
Solvesso #3 1.20 A 15% rubber solution in Solvesso #2 (hydrogenated petroleum solvent-boiling range -177 C.) 1.00 Solvesso #2 22.00
Into this lacquer is emulsified a mixtureof- Parts by weight Sodium chloride l 0.15 35% sulfonated tannin solution 0.12 Acetic acid 0.06 Water 75.47
The alkyd resin is a 40% drying oil modified glycerol phthalate resin, which is freely soluble in hydrogenated petroleum solvents, as distinguished from the alkyd resin of Example 1.
This unpigmented emulsion contains 0.75% solids; the lacquer phase contains about 3% solids. It may be blended with the pigmented emulsion of Example 1 (13.2% solids-lacquer phase about 18% solids) in ratios of 1 to 1 and higher, to produce a three-phase system in which a low-solids clear lacquer the outer phase, and water and resin-solvent aggregate bearing pigment are the inner phases. Microscopic examination of the mixture indicates that the two disperse phases are in very close contact with one another. The mixtures are stable, and prints made therewith show the same resistance to washing and other influences as prints made from Example 1.
7 EXAMPLE 3 Urea. formaldehyde resin An emulsion was made from a lacquer containing- Parts by weight Solvent-soluble urea-formaldehyde resin The lacquer contains about 23% solids, the
emulsion 16%. It can be reduced with the diluting emulsion of Example 2, to give similar results. It may also be reduced with other unpigmented emulsions, such as the following.
Exlmru: 4
Ethyl cellulose reducing emulsion Parts by weight Ethyl cellulose (47% ethoxy-500 centipoise viscosity) 0.4 Pine oil 2.8 Solvesso #2 25.0 Water 72.0
This clear has 0.4%. solids; the has about 1.3% solids.
Exams: 5
Urea-formaldehyde alkyd paste A typical water-in-lacquer printing emulsion may be made as in Example 1 fromlacquer phase Parts by weight Urea resin solution of Example 3 5.0 Alkyd resin solution of Example 1 15.0 Pine oil 5.0 Solvesso 34.0 20% pulp phthalocyanine green 30.0 Water 11.0
This can be reduced with the unpigrnented diluent of Examples 2 and 4, with results similar to Example 2.
Exsurnr: 6
Parts by weight S o l v e n t -s oluble melamine-formaldehyde Urea resin solution of Example 3 Alkyd resin solution of Example 1 510 Pine oil 10.0 Xylene 7.0
The lacquer is then emulsified into Parts by weight Water 46.0 Sodium lauryl sulfate 2.0 Dry bent ni 3.0
phase and reduce the solids content by emulsifyresin (50 resin, 30 butanol, 20 xylene) 4.0 Alkyd resin solution (65 parts alkyd resin of Example 2, 35 parts xylene) 15.5 Solvesso #3 27.5 Benzidine yellowdry basis, but used as pulp 1.6 Water 51.4
Made as in Example 1; it may be reduced with the unpigmented emulsions of Examples 2and4. All of the above examples may be made by first mixing the pigmented lacquers with the clear lacquers of Examples 2 and 4, provided water is immediately emulsified therein; or the clear lacquers of'Examples 2 and 4 maybe added to the emulsions with These methods, however, lack flexibility, since the pigmented emulsion and the diluting emulsion may both be made of printing consistency, so they can be mixed in any desired'proportions before use.
The pigment may be added in pulp form as indicated. or it may be dispersed in conventional fashion.
For overalhpigment covering of textiles, lacquer-in-water emulsions may be used. For example- Exams? Pigment dyeing emulsions Carbon black are dispersed in- Alkyd resin solution. (65 parts" alkyd resin of Example 1, 35' parts xylene) 10.0
and
Xylene 10.0
To the dispersion is added- Parts by weight 2 0 This emulsion contains about 10% resin solids; if applied to cloth direct, it will'produce too still a hand. Reduction of the lacquer with so lvent before emulsiflcation produces pigment flocculation. It is possible to increase the non-aqueous ing the proper solvent into the emulsion with an emulsifying agent. This may be done by making an oil-in-water emulsion from- Parts by weight Solvesso #2 69.00 Oleic acid a v Triethanolamine 0.40 Water 29.35
An excellent pigment dyeing bath is made from 1 part of the pigmented emulsion and 4 or more parts of the unpigmented material.
If desired, the same effect may be obtained by adding water to the pigmented emulsion, then adding the emulsifying agent to the water, and then adding the solvent.
All of the diluted examp1es..when.examined under the microscope, showed the presence of three phases. In the case of the water-in-lacquer emulsions, however, the twodispersed phaseswater and pigment-resin azgrsafe-are insuch close association that they cannot be distin-.
' Parts by weight 5.0
known to the art which will dilute solutions of these resins to a point and beyond that cause precipitation. The choice of the volatile solvents may be left to those skilled in the art, since the phenomenon of precipitation on dilution has been widely studied.
It is only necessary that the diluting solvent contain some emulsifying agent therein so that it may form a stable emulsion; and where high non-volatile (solids) content is undesirable, the solids ofthe diluting low-solids lacquer phase should not exceed about by weight of that phase.
The minimum amount oLaqueous phase needed to prevent separation of the two lacquer phases varies of course with the degree of incompatibility; but in general, of aqueous phase, based on the complete emulsion, is sufiicient. For reasons of economy, and for better working properties, higher amounts are preferable, as indi-' cated in the examples.
The term aggregate as used to describe the pigmented resin-solvent aggregate phase, is used in its popular sense, and not in any technical sense.
I claim:
1. An emulsion comprising an aqueous phase, a phase consisting essentially of a volatile waterimmiscible organic liquid having dissolved therein less than 10% of non-volatile, including an 40 agent capable of producing a stable emulsion of water and said liquid, and adispersed phase of pigmented resin-solvent aggregate derived from a heat-convertible resin lacquer which is miscible with limited quantities of said organic liquid, but immiscible with the quantities employed in the emulsion.
2. A textile decorating emulsion comprising a discontinuous aqueous phase comprising at least 20% by weight of the emulsion, a continuous phase consisting essentially of a volatile waterimmiscible organic liquid having dissolved therein an agent capable of producing a stable emulsion of water and said liquid, and a dispersed phase of pigmented resin-solvent aggregate derived from a pigmented heat-convertible resin lacquer which is miscible with limited quantities of of said organic liquid, but immiscible with the quantities employed in the emulsion.
3. A textile decorating emulsion comprising a discontinuous aqueous phase comprising at least 20% by weight of the emulsion, a continuous phase consisting essentially of a volatile waterimmiscible organic liquid having dissolved therein less than 10% of non-volatile, including an agent capable of producing a stable emulsion of water and said liquid, and a dispersed phase of pigmented resin-solvent aggregate derived from a pigmented heat-convertible resin lacquer which is miscible with limited quantities of said organic liquid but immiscible with the quantities employed in the emulsion.
4. The composition of claim 2, in which the heat-convertible resin comprises a heat-convertible alkyd resin.
5. The composition of claim 2, in which the heat-convertible resin comprises a plasticized urea formaldehyde resin.
6. A textile coloring emulsion comprising an outer continuous aqueous phase and two organic phases, one of which consists essentially of a volatile water-immiscible organic liquid having dissolved therein less than 10% of non-volatile, including an agent capable of producing a stable emulsion of water and said liquid, and the other of which consists of pigmented resin-solvent aggregate derived from a, heat-convertible resin lacquer which is miscible with limited quantities of said organic liquid, but immiscible with the quantities employed in the emulsion.
7. The method of producing a textile decorating emulsion which comprises preparing a waterin-lacquer emulsion, the outer phase of which is pigment dispersed in a lacquer, the binder of which comprises a heat-convertible synthetic resin, the lacquer being of such body that pig'- ment will remain dispersed in it, separately preparing a second water-in-lacquer emulsion, the outer phase of which is a lacquer consisting essentially of volatile solvent having dissolved therein an agent which renders the lacquer capable ofemulsifying water therein, the second lacquer being only partially miscible with the first lacquer, and having a substantially lower nonvolatile content than the first lacquer, and mixing the emulsions to produce an emulsion in which the outer phase consists essentially of the second lacquer, and the inner phases of which comprises water and the first lacquer.
NORMAN S. CASSEL.
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Cited By (15)

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US2462912A (en) * 1945-12-22 1949-03-01 Ct Res Lab Inc Insulating coating having high dielectric strength
US2471396A (en) * 1943-01-01 1949-05-24 American Cyanamid Co Aqueous emulsions of mixed phthalic glyceride and melamine-formalde-hyde resins
US2488544A (en) * 1945-11-28 1949-11-22 Sherwin Williams Co Pad dyeing baths and processes for pad dyeing textile materials
US2494810A (en) * 1945-07-19 1950-01-17 Geigy Co Ltd Pigment emulsions and the manufacture thereof
US2539914A (en) * 1945-08-04 1951-01-30 Sherwin Williams Co Pigment compositions for pad dyeing
US2614086A (en) * 1952-10-14 Bye bath- composition
US2632740A (en) * 1947-12-24 1953-03-24 Ciba Ltd Three-phase emulsion of artificial resins
US2635059A (en) * 1948-10-26 1953-04-14 Edwin L Gustus Resin-impregnated water-resistant leather
US2695895A (en) * 1951-03-10 1954-11-30 American Cyanamid Co Heat-reflective fabrics and method of production
US2718681A (en) * 1951-11-28 1955-09-27 Ciba Ltd Method and compositions for the production of cores for use in metal casting
US2741215A (en) * 1953-02-27 1956-04-10 United Merchants & Mfg Apparatus for coloring raised surface portions of embossed fabric
US2754279A (en) * 1951-08-01 1956-07-10 Minnesota Mining & Mfg Aqueous composition of an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol
US2807557A (en) * 1951-04-16 1957-09-24 Clifford R Carney Method of treating furs
US2992198A (en) * 1956-12-24 1961-07-11 Funahashi Takaji Process of producing liquid color
US4094851A (en) * 1973-10-17 1978-06-13 Monsanto Company Method of preparation of clear concentrate compositions

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2614086A (en) * 1952-10-14 Bye bath- composition
US2471396A (en) * 1943-01-01 1949-05-24 American Cyanamid Co Aqueous emulsions of mixed phthalic glyceride and melamine-formalde-hyde resins
US2494810A (en) * 1945-07-19 1950-01-17 Geigy Co Ltd Pigment emulsions and the manufacture thereof
US2539914A (en) * 1945-08-04 1951-01-30 Sherwin Williams Co Pigment compositions for pad dyeing
US2488544A (en) * 1945-11-28 1949-11-22 Sherwin Williams Co Pad dyeing baths and processes for pad dyeing textile materials
US2462912A (en) * 1945-12-22 1949-03-01 Ct Res Lab Inc Insulating coating having high dielectric strength
US2632740A (en) * 1947-12-24 1953-03-24 Ciba Ltd Three-phase emulsion of artificial resins
US2635059A (en) * 1948-10-26 1953-04-14 Edwin L Gustus Resin-impregnated water-resistant leather
US2695895A (en) * 1951-03-10 1954-11-30 American Cyanamid Co Heat-reflective fabrics and method of production
US2807557A (en) * 1951-04-16 1957-09-24 Clifford R Carney Method of treating furs
US2754279A (en) * 1951-08-01 1956-07-10 Minnesota Mining & Mfg Aqueous composition of an unmodified hydroxyl-containing resinous glycidyl polyether of a dihydric phenol
US2718681A (en) * 1951-11-28 1955-09-27 Ciba Ltd Method and compositions for the production of cores for use in metal casting
US2741215A (en) * 1953-02-27 1956-04-10 United Merchants & Mfg Apparatus for coloring raised surface portions of embossed fabric
US2992198A (en) * 1956-12-24 1961-07-11 Funahashi Takaji Process of producing liquid color
US4094851A (en) * 1973-10-17 1978-06-13 Monsanto Company Method of preparation of clear concentrate compositions

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