US2342641A - Method of coloring textiles - Google Patents
Method of coloring textiles Download PDFInfo
- Publication number
- US2342641A US2342641A US351203A US35120340A US2342641A US 2342641 A US2342641 A US 2342641A US 351203 A US351203 A US 351203A US 35120340 A US35120340 A US 35120340A US 2342641 A US2342641 A US 2342641A
- Authority
- US
- United States
- Prior art keywords
- pigment
- fabric
- emulsion
- lacquer
- resin
- 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.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title description 11
- 239000004753 textile Substances 0.000 title description 11
- 238000004040 coloring Methods 0.000 title 1
- 239000004744 fabric Substances 0.000 description 44
- 239000000049 pigment Substances 0.000 description 29
- 239000000839 emulsion Substances 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 239000011230 binding agent Substances 0.000 description 17
- 239000004922 lacquer Substances 0.000 description 15
- 229920005989 resin Polymers 0.000 description 14
- 239000011347 resin Substances 0.000 description 14
- 238000004043 dyeing Methods 0.000 description 13
- 239000002904 solvent Substances 0.000 description 12
- 239000012071 phase Substances 0.000 description 10
- 238000001035 drying Methods 0.000 description 8
- 230000005012 migration Effects 0.000 description 8
- 238000013508 migration Methods 0.000 description 8
- 239000007787 solid Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000009738 saturating Methods 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 229920001807 Urea-formaldehyde Polymers 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 239000008346 aqueous phase Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005108 dry cleaning Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000005189 flocculation Methods 0.000 description 2
- 230000016615 flocculation Effects 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000010665 pine oil Substances 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000018783 Dacrycarpus dacrydioides Nutrition 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 240000007263 Pinus koraiensis Species 0.000 description 1
- 235000008578 Pinus strobus Nutrition 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000009980 pad dyeing Methods 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- ZDCHZHDOCCIZIY-UHFFFAOYSA-N phthalic acid;propane-1,2,3-triol Chemical group OCC(O)CO.OC(=O)C1=CC=CC=C1C(O)=O ZDCHZHDOCCIZIY-UHFFFAOYSA-N 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000004758 synthetic textile Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General 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
- D06P1/44—General 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S106/00—Compositions: coating or plastic
- Y10S106/04—Bentonite
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/38—Ink
Definitions
- This invention relates to the dyeing of textile fabrics, and has particular reference to a new and novel method of dyeingtextile with pigment lacquers emulsified in water, and to the dye baths used in the method. Specifically, this invention refers to the use as textile dye baths of lacquer emulsions of low binder and pigment content, but containing at least as much lacquer as water by volume.
- Textile fabrics are almost universally colored by being treated with a solution of a dyestuif in an aqueous medium; the soluble dyestufi is precipitated in the capillaries of the fibers of the yarns, or is caused to adhere chemically to the textile material.
- water-insoluble dyestuffs having an affinity for certain synthetic fabrics are used in solution in other .solvents. Since all of these dyestuffs must be capable of conversion from the soluble state to the insoluble state in contact with the fiber, and since they must be resistant to a great variety of deteriorating influences, the problem of inexpensive, fast textile colors has always been a pressing one.
- cloth may be dyed with emulsions of pigmented lacquers in water, while substantially eliminating the tendency of the lacquer to migrate, by dyeing with a bath in which the disperse lacquer phase constitutes at least 50% of the volume of the bath.
- My new method and dye baths may be used successfully with any sort of fabric, and no noticeable migration occurs even on heavy fabrics such as jeans, when the fabrics are dried in conventional fashion by passing the cloth through the ordinary driers used in textile plants.
- pigments and binder may be used for very cheap fabrics such as are used for temporary displays, where light-fastness, washability, resistance to dry cleaning fluids are not essential characteristics, or where the stiffness imparted by the pigment binder is not objectionable.
- the pigments and binders must be chosen with care.
- the pigments must be light-fast, non-bleeding in dry cleaning solvents (petroleum hydrocarbons, carbon tetrachloride, etc.) and resistant to soap, while the binders must also be resistant to the same disintegrating influences, and at the same time bind the pigment to the fabrics even when only small amounts of resin are present on the fabric.
- Heat-convertible synthetic resins are particularly useful, including the urea formaldehyde resins (such as are made by reacting formaldehyde with urea, thiourea, melamine and other homologues and derivatives of urea),the short oil alkyds, and the heat-convertible phenolic resins.
- urea formaldehyde resins such as are made by reacting formaldehyde with urea, thiourea, melamine and other homologues and derivatives of urea
- the short oil alkyds such as are made by reacting formaldehyde with urea, thiourea, melamine and other homologues and derivatives of urea
- the short oil alkyds such as are made by reacting formaldehyde with urea, thiourea, melamine and other homologues and derivatives of urea
- the short oil alkyds such as are made by reacting formaldehyde with urea
- the binder content added to the fabric should not exceed about 2 and since the fabric retains about an equal weight of dyebath, the
- binder content of the dyebath should not in such cases exceed 2% In such cases, and even when higher binder concentrations are used, the lacquer becomes so thin in body (particularly when a heat-convertible resin is the binder) that the pigment tends to flocculate and settle out.
- the added organic phase in such case consists essentially of a volatile solvent having dissolved therein an emulsifying agent, the solvent being of such a character that it is only partially miscible with the organic solvent, so that a three-phase emulsion is obtained.
- an emulsion is described and claimed in my co-pending application, Serial No. 351,206, filed August 8, 1940.
- Typical examples of my invention are the following:
- EXAIPLI 1 Pigment dyeing emulsions Y Parts by weight Carbon black 5.0
- the alkyd resin of this lacquer is glycerol phthalate, modified with 33% soya oil fatty acids; it can be set by heat. It is soluble in aromatic hydrocarbons, and will precipitate on further dilution with aliphatic hydrocarbons. or with mixtures containing substantial quantities of allphatics. The tendency of this lacquer toward immiscibility with added solvents is increased by pigmentation, as with all resin.
- This emulsion contains about 10% resin solids
- An excellent pigment dyeing bath is made from ment dyeing bath, is heated to remove the water and volatile solvent, and to convert the resin to the insoluble state.
- EXAXPLI 2 Yellow emulsion ,Parts by weight A 20% aqueous pulp of yellow pigment, preproducing a stable lacquer-in-water emulsion having 1.3% pigment solids, and 5.5% resin solids. This emulsion is then blended with equal parts by volume of a clear emulsion made as follows:
- sodium lauryl sulfate 1.5 parts of water and 1.5 parts of Aerosol O. T. (sodium salt of alkyl ester of sulfo succinic acid) may be used.
- the method of pigment dyeing a fabric while avoiding substantial migration of color on drying which comprises saturating the fabric with a pigmented lacquer-in-water emulsion, the nonaqueous phase of which comprises at least 50% of the total volume, and drying the fabric.
- the method of pigment dyeing a fabric while avoiding substantial migration of color on drying which comprises saturating the fabric with a pigmented lacquer-in-water emulsion, the nonaqueous phase of which comprises at least 50% of the total volume, the emulsion containing a heat-convertible synthetic resin to bind the pigment -to the fabric, and thereafter heating the fabric to dry it and convert the resin to its insoluble state.
- the method of pigment dyeing a fabric while avoiding substantial migration of color on drying which comprises saturating the fabric with a pigmented lacquer-in-water emulsion, the non-aqueous phase of which comprises at least 50% of the total volume, the emulsion containing a urea formaldehyde resin to bind the pigment to the fabric, and thereafter heating the fabric to dry it and convert the resin to its insoluble state.
- the method of pigment dyeing a fabric while avoiding substantial migration of color on drying which comprises saturating the fabric with a pigmented lacquer-in-water emulsion con taining under about 2 /2% of binder for the pigment, the non-aqueous phase comprising at least 50% of the total volume and consisting of "a pigmented phase containing solvent and heat-convertible resin, and a separate phase consisting essentially of solvent having dissolved therein an agent capable of producing a stable emulsion,
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Description
. unsuccessful.
Patented Feb. 29, 1944 METHOD OF COLQRING TEXTILES Norman S. Cassel, Ridgewood, N. 1., assignor to Interchemical Corporation, New York, N. Y., a
corporation of Ohio No Drawing. Application August 3, 1940, Serial No. 351,203
5 Claims.
This invention relates to the dyeing of textile fabrics, and has particular reference to a new and novel method of dyeingtextile with pigment lacquers emulsified in water, and to the dye baths used in the method. Specifically, this invention refers to the use as textile dye baths of lacquer emulsions of low binder and pigment content, but containing at least as much lacquer as water by volume.
Textile fabrics are almost universally colored by being treated with a solution of a dyestuif in an aqueous medium; the soluble dyestufi is precipitated in the capillaries of the fibers of the yarns, or is caused to adhere chemically to the textile material. In some cases, water-insoluble dyestuffs having an affinity for certain synthetic fabrics are used in solution in other .solvents. Since all of these dyestuffs must be capable of conversion from the soluble state to the insoluble state in contact with the fiber, and since they must be resistant to a great variety of deteriorating influences, the problem of inexpensive, fast textile colors has always been a pressing one.
The ready availability and low cost of the insoluble pigment colors has prompted many investigators to study the application of these colors for the dyeing of textiles, but with relatively little success. Except where the pigment is incorporated into a spinning solution used for making synthetic fibers, unaided mechanical adhesion of the pigment to the yarns has proven Attempts to cause the pigment to adhere to the fabric by the use of binders have likewise proven abortive, for a variety of reasons. A principal cause has been the failure of the pigment binders to withstand the severe condi tions to which textile are subjected; the failure of the binder leaves the pigment in mere mechanical contact with the fabric, whence it is easily removed. A second important difficulty has been that of even application of very small quantities of pigment plus binder, so that the fabric is colored uniformly. The problem is presented by the tendency of pigments to flocculate or settle out in highly disperse media, so that uniform application is very'diflicult.
It has been proposed to dye textile fabrics with pigmented lacquers emulsified as the discontinuous phase of a lacquer-in-water emulsion, using heat-convertible synthetic resins as binder in the lacquer. Such emulsions give satisfactory uniform dyeings on fabrics, when the fabrics are immersed in the bath and the excess color squeezed off. However, the cloth must be heated after the dyeing operation, both to evaprate the water and solvent, and to set the resin. the fabric is not maintained in a uniform state of tension, or if the drying is done unevenly, the color will tend to migrate and give a streaked appearance. This tendency is considerably aggravated as cloth, thickness increases, so that shirting broadcloths and heavier fabrics must be handled with special equipment and with such extreme care that rapid drying is impossible. As a result, the emulsion pad dyeing has for the most part been restricted to rather thin fabrics, or to special cases with heavier fabrics.
I have discovered that cloth may be dyed with emulsions of pigmented lacquers in water, while substantially eliminating the tendency of the lacquer to migrate, by dyeing with a bath in which the disperse lacquer phase constitutes at least 50% of the volume of the bath.
My new method and dye baths may be used successfully with any sort of fabric, and no noticeable migration occurs even on heavy fabrics such as jeans, when the fabrics are dried in conventional fashion by passing the cloth through the ordinary driers used in textile plants.
Substantially any combination of pigments and binder may be used for very cheap fabrics such as are used for temporary displays, where light-fastness, washability, resistance to dry cleaning fluids are not essential characteristics, or where the stiffness imparted by the pigment binder is not objectionable. In the dyeing of better grade fabrics, however, where these factors are of importance, the pigments and binders must be chosen with care. The pigments must be light-fast, non-bleeding in dry cleaning solvents (petroleum hydrocarbons, carbon tetrachloride, etc.) and resistant to soap, while the binders must also be resistant to the same disintegrating influences, and at the same time bind the pigment to the fabrics even when only small amounts of resin are present on the fabric. Heat-convertible synthetic resins are particularly useful, including the urea formaldehyde resins (such as are made by reacting formaldehyde with urea, thiourea, melamine and other homologues and derivatives of urea),the short oil alkyds, and the heat-convertible phenolic resins.
Where a heavy finish is undesirable on the fabric, the binder content added to the fabric should not exceed about 2 and since the fabric retains about an equal weight of dyebath, the
binder content of the dyebath should not in such cases exceed 2% In such cases, and even when higher binder concentrations are used, the lacquer becomes so thin in body (particularly when a heat-convertible resin is the binder) that the pigment tends to flocculate and settle out. I
or without water. The added organic phase in such case consists essentially of a volatile solvent having dissolved therein an emulsifying agent, the solvent being of such a character that it is only partially miscible with the organic solvent, so that a three-phase emulsion is obtained. Such an emulsion is described and claimed in my co-pending application, Serial No. 351,206, filed August 8, 1940.
It consists essentially of an outer water phase having two dispersed lacquer phases, one of which is a pigmented resin solvent aggregate, and the other of which consists essentially of a volatile solvent having dissolved therein sumcient emulsitying agent to make the emulsion stable. but under non-volatile based on the weight of this phase by preference.
Typical examples of my invention are the following:
EXAIPLI 1 Pigment dyeing emulsions Y Parts by weight Carbon black 5.0
are dispersed in The alkyd resin of this lacquer is glycerol phthalate, modified with 33% soya oil fatty acids; it can be set by heat. It is soluble in aromatic hydrocarbons, and will precipitate on further dilution with aliphatic hydrocarbons. or with mixtures containing substantial quantities of allphatics. The tendency of this lacquer toward immiscibility with added solvents is increased by pigmentation, as with all resin.
This emulsion contains about 10% resin solids;
The cloth, after impregnation with the pigif applied to cloth direct, it will produce too stii! a hand. Reduction of the lacquer with solvent before emulsiflcation produces pigment flocculation. It is possible to increase the non-aqueous phase and reduce the solids content by emulsifying the propersolvent into the emulsion with an emulsifying agent. This may be done by making an oil-inwater emulsion from- Parts by t weight Solvesso #2 (hydrogenated petroleum solvent--b0i1ing range 135-177' C.) '69 .00 Oleic acid 1.25 Triethanolamine 0.40 Water 29.35
An excellent pigment dyeing bath is made from ment dyeing bath, is heated to remove the water and volatile solvent, and to convert the resin to the insoluble state.
EXAXPLI 2 Yellow emulsion ,Parts by weight A 20% aqueous pulp of yellow pigment, preproducing a stable lacquer-in-water emulsion having 1.3% pigment solids, and 5.5% resin solids. This emulsion is then blended with equal parts by volume of a clear emulsion made as follows:
Exams: 3
Clear emulsion 50 parts by weight of a lacquer consisting of Parts by weight Urea formaldehyde resin solution of Example 1 l0 Alkyd resin of Example 1, 50% solution in pine oil 30 White pine oil 5 Solvesso 55 are added slowly, with stirring to a solution 01- Sodium lauryl sulfate 2.5 Water 47.5
to produce a stable clear lacquer-in-water emulsion containing 10% resin solids.
For the 2.5 parts of sodium lauryl sulfate, 1.5 parts of water and 1.5 parts of Aerosol O. T. (sodium salt of alkyl ester of sulfo succinic acid) may be used.
When applied alone, too much hand is ob-- tained. When diluted with water, migration occurs. When diluted as suggested in Example 1, the resultant fabric is soft, and no migration occurs on drying. 1
Obviously the examples may be multiplied indefinitely without departing from the scope of my invention, which is defined in the claims. Obviously, while I have shown only preferred binders in my examples, natural resins, cellulose esters and ethers, natural and synthetic rubber, and other pigment-binding substances may be applied to cloth in the indicated fashion, while avoiding migration. While my method of diluting the emulsions to'obtain. a low solid content is highly desirable, especially with heat-convertible resins, it is not essential where the pigment may be dispersed without flocculation otherwise, as with high viscosity cellulose derivatives.
I claim:
1. The method of pigment dyeing a fabric while avoiding substantial migration of color on drying, which comprises saturating the fabric with a pigmented lacquer-in-water emulsion, the nonaqueous phase of which comprises at least 50% of the total volume, and drying the fabric.
2. The method of pigment dyeing a fabric while avoiding substantial migration of color on drying, which comprises saturating the fabric with a pigmented lacquer-in-water emulsion, the nonaqueous phase of which comprises at least 50% of the total volume, the emulsion containing a heat-convertible synthetic resin to bind the pigment -to the fabric, and thereafter heating the fabric to dry it and convert the resin to its insoluble state.
3. The method of pigment dyeing a fabric while avoiding substantial migration of color on drying, which comprises saturating the fabric with a pigmented lacquer-in-water emulsion, the non-aqueous phase of which comprises at least 50% of the total volume, the emulsion containing a urea formaldehyde resin to bind the pigment to the fabric, and thereafter heating the fabric to dry it and convert the resin to its insoluble state.
a 4. The method of claim 1 in which the binder content of the lacquer is under about 2 of the emulsion weight.
5. The method of pigment dyeing a fabric while avoiding substantial migration of color on drying, which comprises saturating the fabric with a pigmented lacquer-in-water emulsion con taining under about 2 /2% of binder for the pigment, the non-aqueous phase comprising at least 50% of the total volume and consisting of "a pigmented phase containing solvent and heat-convertible resin, and a separate phase consisting essentially of solvent having dissolved therein an agent capable of producing a stable emulsion,
and thereafter heating the fabric to dry it and convert the resin to its insoluble state.
NORMAN S. CASSEL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US351203A US2342641A (en) | 1940-08-03 | 1940-08-03 | Method of coloring textiles |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US351203A US2342641A (en) | 1940-08-03 | 1940-08-03 | Method of coloring textiles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2342641A true US2342641A (en) | 1944-02-29 |
Family
ID=23380001
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US351203A Expired - Lifetime US2342641A (en) | 1940-08-03 | 1940-08-03 | Method of coloring textiles |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2342641A (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2416103A (en) * | 1943-10-30 | 1947-02-18 | United Aircraft Corp | Deicing composition |
| US2424284A (en) * | 1943-02-22 | 1947-07-22 | British Celanese | Fixation of finely divided substances |
| US2426194A (en) * | 1944-04-04 | 1947-08-26 | Fischbach Adolph | Ink |
| US2446864A (en) * | 1944-06-26 | 1948-08-10 | Quaker Chemical Products Corp | Composition and process for imparting durable water repellent finish to textiles |
| US2524112A (en) * | 1945-09-28 | 1950-10-03 | Stein Hall & Co Inc | Resinous composition and method of making same |
| US2524111A (en) * | 1945-09-28 | 1950-10-03 | Stein Hall & Co Inc | Resinous composition and method of making same |
| US2539914A (en) * | 1945-08-04 | 1951-01-30 | Sherwin Williams Co | Pigment compositions for pad dyeing |
| US2632740A (en) * | 1947-12-24 | 1953-03-24 | Ciba Ltd | Three-phase emulsion of artificial resins |
| US2633433A (en) * | 1946-05-02 | 1953-03-31 | Baldwin Hill Company | Insulating material |
| US2637711A (en) * | 1950-06-22 | 1953-05-05 | Auer Laszlo | Pigment dispersions in water |
| DE875942C (en) * | 1945-07-19 | 1953-05-07 | Ciba Geigy | Process for matting or coloring fibers |
| US2704750A (en) * | 1951-07-03 | 1955-03-22 | Sherwin Williams Co | Aminoplast resins |
| US2956907A (en) * | 1954-04-01 | 1960-10-18 | Bayer Ag | Dyeing of fabrics by means of pigments |
| WO2014056563A1 (en) | 2012-10-09 | 2014-04-17 | Clariant International Ltd | Dispersing agent from renewable raw materials for binding agent-free pigment preparations |
-
1940
- 1940-08-03 US US351203A patent/US2342641A/en not_active Expired - Lifetime
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2424284A (en) * | 1943-02-22 | 1947-07-22 | British Celanese | Fixation of finely divided substances |
| US2416103A (en) * | 1943-10-30 | 1947-02-18 | United Aircraft Corp | Deicing composition |
| US2426194A (en) * | 1944-04-04 | 1947-08-26 | Fischbach Adolph | Ink |
| US2446864A (en) * | 1944-06-26 | 1948-08-10 | Quaker Chemical Products Corp | Composition and process for imparting durable water repellent finish to textiles |
| DE875942C (en) * | 1945-07-19 | 1953-05-07 | Ciba Geigy | Process for matting or coloring fibers |
| US2539914A (en) * | 1945-08-04 | 1951-01-30 | Sherwin Williams Co | Pigment compositions for pad dyeing |
| US2524112A (en) * | 1945-09-28 | 1950-10-03 | Stein Hall & Co Inc | Resinous composition and method of making same |
| US2524111A (en) * | 1945-09-28 | 1950-10-03 | Stein Hall & Co Inc | Resinous composition and method of making same |
| US2633433A (en) * | 1946-05-02 | 1953-03-31 | Baldwin Hill Company | Insulating material |
| US2632740A (en) * | 1947-12-24 | 1953-03-24 | Ciba Ltd | Three-phase emulsion of artificial resins |
| US2637711A (en) * | 1950-06-22 | 1953-05-05 | Auer Laszlo | Pigment dispersions in water |
| US2704750A (en) * | 1951-07-03 | 1955-03-22 | Sherwin Williams Co | Aminoplast resins |
| US2956907A (en) * | 1954-04-01 | 1960-10-18 | Bayer Ag | Dyeing of fabrics by means of pigments |
| WO2014056563A1 (en) | 2012-10-09 | 2014-04-17 | Clariant International Ltd | Dispersing agent from renewable raw materials for binding agent-free pigment preparations |
| US9303143B2 (en) | 2012-10-09 | 2016-04-05 | Clariant International Ltd. | Dispersing agent from renewable raw materials for binding agent-free pigment preparations |
| US9303144B2 (en) | 2012-10-09 | 2016-04-05 | Clariant International Ltd. | Dispersing agent from renewable raw materials for binding agent-free pigment preparations |
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