US2342641A - Method of coloring textiles - Google Patents

Method of coloring textiles Download PDF

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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
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Prior art keywords
pigment
fabric
emulsion
lacquer
resin
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US351203A
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Norman S Cassel
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Interchemical Corp
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Interchemical Corp
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Classifications

    • 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
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S106/00Compositions: coating or plastic
    • Y10S106/04Bentonite
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S260/00Chemistry of carbon compounds
    • Y10S260/38Ink

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,

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  • 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.
US351203A 1940-08-03 1940-08-03 Method of coloring textiles Expired - Lifetime US2342641A (en)

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Cited By (14)

* Cited by examiner, † Cited by third party
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

Cited By (16)

* Cited by examiner, † Cited by third party
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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