US2770518A - Dyed textile materials and method of making - Google Patents

Dyed textile materials and method of making Download PDF

Info

Publication number
US2770518A
US2770518A US315824A US31582452A US2770518A US 2770518 A US2770518 A US 2770518A US 315824 A US315824 A US 315824A US 31582452 A US31582452 A US 31582452A US 2770518 A US2770518 A US 2770518A
Authority
US
United States
Prior art keywords
dyed
textile material
alkyl
polymeric
fading
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
Application number
US315824A
Inventor
Anthony B Conciatori
Victor S Salvin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Celanese Corp
Original Assignee
Celanese Corp
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 Celanese Corp filed Critical Celanese Corp
Priority to US315824A priority Critical patent/US2770518A/en
Application granted granted Critical
Publication of US2770518A publication Critical patent/US2770518A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • D06P1/52General 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 using compositions containing synthetic macromolecular substances
    • D06P1/5207Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • D06P1/525Polymers of unsaturated carboxylic acids or functional derivatives thereof
    • D06P1/5257(Meth)acrylic acid
    • 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
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/92Synthetic fiber dyeing
    • Y10S8/921Cellulose ester or ether
    • 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
    • Y10S8/00Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
    • Y10S8/92Synthetic fiber dyeing
    • Y10S8/924Polyamide fiber

Definitions

  • This invention relates to dyed textile materials and relates more particularly to dyed textile materials having an improved resistance to gas fading.
  • An important object of this invention is the preparation of dyed textile materials that exhibit an improved resistance to gas fading.
  • a further object of this invention is to provide dyed textile materials of improved resistance to gas fading having applied thereto a polymeric dialkyl-amino-alkylacrylate.
  • the change which occurs may be a dulling of the brightness of the shade in some instances and in others there may be a definite change in color.
  • These undesirable effects are frequently observed in the case of many anthraquinone dyestuffs which yield valuable blue colors on these textile materials.
  • textile materials dyed with these colors are exposed to acid fumes the colors change from a pure blue shade to one having a reddish cast.
  • the blue color may even change to a pink color.
  • Such changes obviously restrict the range of usefulness of these dyestuffs. Ac cordingly, methods of increasing the resistance of these dyes to gas fading are of great commercial importance.
  • the gas fading characteristics of dyed textile materials that exhibit a tendency to gas fading may be substantially improved if there is applied to said textile materials a polymeric dialkyl-amino-alkylacrylate whose alkyl and alkylene groups contain up to 6 carbon atoms.
  • the salts of the polymeric material such as the acetates and the like, are soluble in water and may be applied to the textile material from aqueous solution, reducing the expense of such application to a minimum.
  • the polymeric material may also be applied to the textile material from solution in an organic solvent or as an emulsion. Following the application of the polymeric.
  • polymeric dialkyl-amino-alkylacryl-ates examples include, for example, polymeric dimethylaminoethylmethacrylate, polymeric diethylaminoethylmethacrylate, polydimethylaminoethylacrylate, polydiethylamin'oethylacrylate, polymeric dimethylaminomethylacrylate, and the like.
  • the quantity of polymeric materials applied may range from about 0.5 to 5.0 percent by weight based on the weight of the textile material.
  • the polymeric materials are themselves strongly resistant to discoloration during exposure to acid fumes so that they will not cause an undesirable change in the coloration of the dyed textile materials.
  • a white satin fabric formed of cellulose acetate yarns is padded with 1 percent of its weight of the acetate salt of polydimethylaminoethylmethacrylate, and then dried and baked for 1 hour at a temperature of 110 C, the fabric shows substantially no discoloration when exposed to gas-fading conditions.
  • Example I A sadn fabric formed of cellulose acetate yarns dyed with 2% by weight on the weight of the fabric of l-4 clialkylamino anthraquinone is padded with 1 percent by weight on the weight of the fabric of the acetate salt lOf poly-dimethylaminoethylmethacrylate and dried. The dried fabric retained its color substantially unchanged on exposure to 3 units of gas fading according to the standard A. A. T. C. C. gas-fading test and showed only a slight reddening on exposure of 4 units of gas fading.
  • Example 11 A dyed fabric treated in the manner set forth in Example I is baked for 1 hour at a temperature of 110 C. and scoured. On exposure in a gas fading apparatus, the fabric exhibits substantially the same resistance to gas fading as exhibited by the fabric in Example 1. However, if the fabric is scoured without baking it loses substantially all of its resistance to gas fading.
  • Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to. gasfading on said material which comprises applying a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material.
  • Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gasfading on said material which comprises applying from about 0.5 to 5.0 percent by weight of a polymeric dialkyl-arnin'o-alkyl-acrylate wherein the alkyl and alkyldyed textile material.
  • Process for improving'the resistance to gas fading of a ,dyed cellulose acetate textilematerial dyed with a blue anthraquinone dye exhibiting a tendency to gas fading which comprises applying a polymeric dialkylamino-alkylacrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material.
  • Process for improving the resistance to gas fading of a dyed cellulose acetate textile material dyed with a blue anthraquinone dye exhibiting a tendency to gas fading which comprises applying polymeric dimethylaminoethylmethacrylate to the said dyed textile material.
  • Process for improving the resistance to gas fading of a dyed cellulose acetate textile material dyed with a blue anthraquinone dye exhibiting a tendency to gas fading which comprises applying from about 0.5 to 5.0 percent by Weight of polymeric dimethylaminoethylmethacrylate to the said dyed textile material.
  • Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gasfading on said material which comprises applying a polymeric dialkyl-alnino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material, and baking the textile material at an elevated temperature.
  • Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas-fading lOn said material which comprises applying a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material, and baking the textile material at a temperature of at least about 100 C. for 1 material at a temperature of about 160 C. for a period 1 of about 10 minutes.
  • Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas-fading on said material which comprises applying a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material, and baking the textile material at a temperature of about 110 C. for a period of about one hour.
  • a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms.
  • a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto from about 0.5 to 5.0 percent of a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms.
  • a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto polymeric dimethylaminoethylmethacrylate.
  • a dyed textile material having a basis of an ester selected from the group consisting 10f cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto from about 0.5 to 5.0 percent lof polymeric dimethylamin'oethylmethacrylate to improve its resistance to gas fading.
  • a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms which has been baked at an elevated temperature.
  • a dyed textile material having a basis 10f an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms which has been baked at a temperature of about C. for a period of about 10 minutes.

Description

United States DYED TEXTILE MATERIALS AND METHOD OF MAKING No Drawing. Application October 20, 1952, Serial No. 315,82
16 Claims. (Cl. 8--1$) This invention relates to dyed textile materials and relates more particularly to dyed textile materials having an improved resistance to gas fading.
An important object of this invention is the preparation of dyed textile materials that exhibit an improved resistance to gas fading.
A further object of this invention is to provide dyed textile materials of improved resistance to gas fading having applied thereto a polymeric dialkyl-amino-alkylacrylate.
Other objects of this invention will be apparent from the following detailed description and claims.
In the coloration of textile materials it is very desirable that the colors obtained be as fast as possible to light, Washing and other agencies, such as acid fumes. It has been found that on certain types of textile materials including organic acid esters of cellulose, such as cellulose acetate, and linear polyesters, such as polyethylene glycol terephthalate, many dyestuffs yield colors that are fast to light and washing, but these colors stiffer from a lack of fastness to acid fumes. When textile materials to which these dyestuffs have been applied are exposed to acid fumes, such as, for example, the products of combustion of coal, gas, etc., the color undergoes a change in shade. This change is usually referred to as gas fading. The change which occurs may be a dulling of the brightness of the shade in some instances and in others there may be a definite change in color. These undesirable effects are frequently observed in the case of many anthraquinone dyestuffs which yield valuable blue colors on these textile materials. When textile materials dyed with these colors are exposed to acid fumes the colors change from a pure blue shade to one having a reddish cast. On continued exposure to the acid fumes the blue color may even change to a pink color. Such changes obviously restrict the range of usefulness of these dyestuffs. Ac cordingly, methods of increasing the resistance of these dyes to gas fading are of great commercial importance.
We have now found that the gas fading characteristics of dyed textile materials that exhibit a tendency to gas fading may be substantially improved if there is applied to said textile materials a polymeric dialkyl-amino-alkylacrylate whose alkyl and alkylene groups contain up to 6 carbon atoms. The salts of the polymeric material, such as the acetates and the like, are soluble in water and may be applied to the textile material from aqueous solution, reducing the expense of such application to a minimum. The polymeric material may also be applied to the textile material from solution in an organic solvent or as an emulsion. Following the application of the polymeric.
atent O "ice C. for a period of at least about 5 minutes. The higher the temperature of baking the shorter the baking period needed to render the resistance to gas fading fast to washing. For example, the improvement in. wash-fastness obtained by baking in 5 minutes at 160 C. is similar to that obtained in 30 minutes at C., While a 10 minute baking at C. yields results which are even better than those obtained in one hour at 110 C.
Examples of suitable polymeric dialkyl-amino-alkylacryl-ates that may be employed in carrying out this invention include, for example, polymeric dimethylaminoethylmethacrylate, polymeric diethylaminoethylmethacrylate, polydimethylaminoethylacrylate, polydiethylamin'oethylacrylate, polymeric dimethylaminomethylacrylate, and the like. The quantity of polymeric materials applied may range from about 0.5 to 5.0 percent by weight based on the weight of the textile material. The polymeric materials are themselves strongly resistant to discoloration during exposure to acid fumes so that they will not cause an undesirable change in the coloration of the dyed textile materials. Thus, when a white satin fabric formed of cellulose acetate yarns is padded with 1 percent of its weight of the acetate salt of polydimethylaminoethylmethacrylate, and then dried and baked for 1 hour at a temperature of 110 C, the fabric shows substantially no discoloration when exposed to gas-fading conditions.
The following examples are given to illustrate this invention further:
Example I A sadn fabric formed of cellulose acetate yarns dyed with 2% by weight on the weight of the fabric of l-4 clialkylamino anthraquinone is padded with 1 percent by weight on the weight of the fabric of the acetate salt lOf poly-dimethylaminoethylmethacrylate and dried. The dried fabric retained its color substantially unchanged on exposure to 3 units of gas fading according to the standard A. A. T. C. C. gas-fading test and showed only a slight reddening on exposure of 4 units of gas fading.
Example 11 A dyed fabric treated in the manner set forth in Example I is baked for 1 hour at a temperature of 110 C. and scoured. On exposure in a gas fading apparatus, the fabric exhibits substantially the same resistance to gas fading as exhibited by the fabric in Example 1. However, if the fabric is scoured without baking it loses substantially all of its resistance to gas fading.
it is to be understood that the foregoing detailed description is given merely by way of illustration and that many variations may be made therein without departing from the spirit of our invention.
Having described our invention what we desire to secure by Letters Patent is:
1. Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to. gasfading on said material, which comprises applying a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material.
2. Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gasfading on said material, which comprises applying from about 0.5 to 5.0 percent by weight of a polymeric dialkyl-arnin'o-alkyl-acrylate wherein the alkyl and alkyldyed textile material.
3. Process for improving'the resistance to gas fading of a ,dyed cellulose acetate textilematerial dyed with a blue anthraquinone dye exhibiting a tendency to gas fading, which comprises applying a polymeric dialkylamino-alkylacrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material.
4. Process for improving the resistance to gas fading of a dyed cellulose acetate textile material dyed with a blue anthraquinone dye exhibiting a tendency to gas fading, which comprises applying polymeric dimethylaminoethylmethacrylate to the said dyed textile material.
5. Process for improving the resistance to gas fading of a dyed cellulose acetate textile material dyed with a blue anthraquinone dye exhibiting a tendency to gas fading, which comprises applying from about 0.5 to 5.0 percent by Weight of polymeric dimethylaminoethylmethacrylate to the said dyed textile material.
6. Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gasfading on said material, which comprises applying a polymeric dialkyl-alnino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material, and baking the textile material at an elevated temperature.
7. Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas-fading lOn said material, which comprises applying a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material, and baking the textile material at a temperature of at least about 100 C. for 1 material at a temperature of about 160 C. for a period 1 of about 10 minutes.
9. Process for improving the resistance to gas fading of a dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas-fading on said material, which comprises applying a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms to the said dyed textile material, and baking the textile material at a temperature of about 110 C. for a period of about one hour.
10. A dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms.
11. A dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto from about 0.5 to 5.0 percent of a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms.
12. A dyed cellulose acetate textile material dyed with a blue anthraquinone dye which normally exhibits a tendency to gas-fading on said material, said textile mate rial having applied thereto a polymeric dialkyl-aminoalkyl-aorylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms.
13. A dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto polymeric dimethylaminoethylmethacrylate.
14. A dyed textile material having a basis of an ester selected from the group consisting 10f cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto from about 0.5 to 5.0 percent lof polymeric dimethylamin'oethylmethacrylate to improve its resistance to gas fading.
15. A dyed textile material having a basis of an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms which has been baked at an elevated temperature.
16. A dyed textile material having a basis 10f an ester selected from the group consisting of cellulose acetate and polyethylene terephthalate and dyed with a blue anthraquinone dye which exhibits a tendency to gas fading on said material, said dyed textile material having applied thereto a polymeric dialkyl-amino-alkyl-acrylate wherein the alkyl and alkylene groups contain at most 6 carbon atoms which has been baked at a temperature of about C. for a period of about 10 minutes.
References Cited in the file of this patent UNITED STATES PATENTS MacGregor Mar. 11, 1947

Claims (1)

1. PROCESS FOR IMPROVING THE RESISTANCE TO GAS FADING OF A DYED TEXTILE MATERIAL HAVING A BASIS OF AN ESTER SELECTED FROM THE GROUP CONSISTING OF CELLULOSE ACETATE AND POLYETHYLENE TEREPHTHALATE AND DYED WITH A BLUE ANTHRAQUINONE DYE WHICH EXHIBITS A TENDENCY TO GASFADING ON SAID MATERIAL, WHICH COMPRISES APPLYING A POLYMERIC DIALKYL-AMINO-ALKYL-ACRYLATE WHEREIN THE ALKYL AND ALKYLENE GROUP CONTAIN AT MOST 6 CARBON ATOMS TO THE SAID DYED TEXTILE MATERIAL.
US315824A 1952-10-20 1952-10-20 Dyed textile materials and method of making Expired - Lifetime US2770518A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US315824A US2770518A (en) 1952-10-20 1952-10-20 Dyed textile materials and method of making

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US315824A US2770518A (en) 1952-10-20 1952-10-20 Dyed textile materials and method of making

Publications (1)

Publication Number Publication Date
US2770518A true US2770518A (en) 1956-11-13

Family

ID=23226215

Family Applications (1)

Application Number Title Priority Date Filing Date
US315824A Expired - Lifetime US2770518A (en) 1952-10-20 1952-10-20 Dyed textile materials and method of making

Country Status (1)

Country Link
US (1) US2770518A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2870044A (en) * 1956-03-27 1959-01-20 Du Pont Coated polymeric thermoplastic dielectric film
US3099636A (en) * 1960-05-17 1963-07-30 Du Pont Polymeric acid salts of alkylaminoethyl methacrylate
US3244544A (en) * 1961-11-21 1966-04-05 Walter G Scharf Method of fabricating prismatic yarn and the resulting product
US4490494A (en) * 1971-12-13 1984-12-25 Phillips Petroleum Company Dyeable polymer alloy fibers containing a polymeric dye-receptor and a metal salt of a carboxylic acid

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2138762A (en) * 1935-05-16 1938-11-29 Du Pont Process of polymerizing methacrylic esters of amino alcohols, in which the amino group is tertiary, and product
US2138763A (en) * 1938-03-30 1938-11-29 Du Pont Amino alcohol esters of the alpha substituted acrylic acids
US2368948A (en) * 1941-04-24 1945-02-06 Rohm & Haas Process for increasing the transparency of fabrics containing filament yarns
US2417312A (en) * 1943-07-22 1947-03-11 Courtaulds Ltd Improving the dyeing properties of cellulosic textiles by treatment with formaldehyde and a guanidine salt of an alpha-beta unsaturated carboxylic acid

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2138762A (en) * 1935-05-16 1938-11-29 Du Pont Process of polymerizing methacrylic esters of amino alcohols, in which the amino group is tertiary, and product
US2138763A (en) * 1938-03-30 1938-11-29 Du Pont Amino alcohol esters of the alpha substituted acrylic acids
US2368948A (en) * 1941-04-24 1945-02-06 Rohm & Haas Process for increasing the transparency of fabrics containing filament yarns
US2417312A (en) * 1943-07-22 1947-03-11 Courtaulds Ltd Improving the dyeing properties of cellulosic textiles by treatment with formaldehyde and a guanidine salt of an alpha-beta unsaturated carboxylic acid

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2870044A (en) * 1956-03-27 1959-01-20 Du Pont Coated polymeric thermoplastic dielectric film
US3099636A (en) * 1960-05-17 1963-07-30 Du Pont Polymeric acid salts of alkylaminoethyl methacrylate
US3244544A (en) * 1961-11-21 1966-04-05 Walter G Scharf Method of fabricating prismatic yarn and the resulting product
US4490494A (en) * 1971-12-13 1984-12-25 Phillips Petroleum Company Dyeable polymer alloy fibers containing a polymeric dye-receptor and a metal salt of a carboxylic acid

Similar Documents

Publication Publication Date Title
US2770518A (en) Dyed textile materials and method of making
US2017119A (en) Treatment of textile and other materials
DE1146030B (en) Process for dyeing and printing fiber material made from aromatic polyesters
US3113825A (en) Dyeing of viscose
DE1284087B (en) Dyeing synthetic linear polyesters
US3092435A (en) Process of dyeing polyethylene and polypropylene materials
US2546168A (en) Emulsions of water-insoluble organic acid-fading inhibitors dissolved in water-insoluble organic solvents
US1914945A (en) Coloration of materials
US2772169A (en) Antioxidant material and use of said material in treating meat
DE1694412A1 (en) Bulk dyeing process for synthetic linear polyesters
US2760841A (en) Dyeing of mixed cellulose derivative-
US2706142A (en) Treatment of dyed cellulose esters and ethers to inhibit gas fading
US2340375A (en) Treatment of cellulose esters and ethers
US3072683A (en) 1-amino-4-sulfonamidoanthraquinone compounds comtaining an ether group in the 2-position
US2764467A (en) Process of inhibiting acid fading and the products thereof
US2409257A (en) Acid fading inhibition
US2659739A (en) 1-hydroxy-4-beta-cyanopropylamino-anthraquinone and process for preparing same
US3379738A (en) 2-anilino-1, 4-dihydroxyanthraquinones
US3445485A (en) 1-amino-2 methylolcyclo-hexylmethoxy-4-hydroxy-anthraquinones
US3495929A (en) Method for improving the fastness to gas fading of dyed material
US2863860A (en) New monoazo compounds
US3359230A (en) Process for the mass coloration of polyesters
US2992064A (en) Gas-fading inhibitor for dyed textiles
US2960381A (en) Dyeing of threads, filaments, fibres and the like
US3012978A (en) Process of treating filaments with a peroxygen compound