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
  • D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
  • D06P3/70—Material containing nitrile groups
  • D06P3/76—Material containing nitrile groups using basic dyes
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
  • D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
  • D06L1/02—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using organic solvents
  • D06L1/06—De-sizing
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
  • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
  • D06L4/60—Optical bleaching or brightening
  • D06L4/664—Preparations of optical brighteners; Optical brighteners in aerosol form; Physical treatment of optical brighteners
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
  • D06M23/10—Processes in which the treating agent is dissolved or dispersed in organic solvents; Processes for the recovery of organic solvents thereof
• • 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
  • D06P1/46—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 using compositions containing natural macromolecular substances or derivatives thereof
  • D06P1/48—Derivatives of carbohydrates
  • D06P1/50—Derivatives of cellulose
• • 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
  • D06P1/62—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 using compositions containing low-molecular-weight organic compounds with sulfate, sulfonate, sulfenic or sulfinic groups
  • D06P1/621—Compounds without nitrogen
  • D06P1/622—Sulfonic acids or their salts
  • D06P1/623—Aliphatic, aralophatic or cycloaliphatic
• • 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
  • D06P1/653—Nitrogen-free carboxylic acids or their salts
  • D06P1/6533—Aliphatic, araliphatic or cycloaliphatic
• • 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
  • D06P1/90—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 dyes dissolved in organic solvents or aqueous emulsions thereof
  • D06P1/92—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 dyes dissolved in organic solvents or aqueous emulsions thereof in organic solvents
  • D06P1/922—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 dyes dissolved in organic solvents or aqueous emulsions thereof in organic solvents hydrocarbons
  • D06P1/924—Halogenated hydrocarbons
• • 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
  • D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
  • D06P3/02—Material containing basic nitrogen
  • D06P3/04—Material containing basic nitrogen containing amide groups
  • D06P3/24—Polyamides; Polyurethanes
  • D06P3/241—Polyamides; Polyurethanes using acid dyes
• • 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
  • D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
  • D06P3/34—Material containing ester groups
  • D06P3/52—Polyesters
  • D06P3/54—Polyesters using dispersed dyestuffs
• • 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
  • D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
  • D06P3/58—Material containing hydroxyl groups
  • D06P3/60—Natural or regenerated cellulose
  • D06P3/64—Natural or regenerated cellulose using mordant dyes or metallisable dyes
• • 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
  • Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
  • Y10S8/92—Synthetic fiber dyeing
  • Y10S8/924—Polyamide fiber

Definitions

• This invention relates to improved emulsions in halogenated hydrocarbon solvents of dyestuffs and textile finishing agents, and to the use of such emulsions in the dyeing and finishing of textile fabrics.
• a stabilised emulsion in a halogenated hydrocarbon solvent of an aqueous solution or an aqueous dispersion of a dyestuff or a textile finishing agent characterised in that the emulsion contains as emulsifying agents ethyl hydroxyethyl cellulose and at least one anionic surface active agent.
• ethyl hydroxyethyl cellulose is meant a mixed cellulose ether which is prepared by a process involving the following three reactions l. alkali cellulose formation in which cellulose is swollen by aqueous sodium hydroxide; Cell OH 1+ NaOl-l Cell OI-l.NaOl-l;
• Ethyl hydroxyethyl cellulose is available commercially in a number of different grades depending on its molecular weight. These grades may be characterised by their solution viscosities, ranging from to 250 cp.
• ethyl hy- I droxyethyl cellulose is suitable for use in the emulsions of the present invention, but the grade having a solution viscosity as hereinbefore-defined of 20 35 cp is preferred.
• Anionic surface active agents which are suitable for use in the emulsions of the invention include salts of sulphonated castor oil, known collectively commermore such agents may be employed.
• Halogenated hydrocarbon solvents which may be employed in the emulsions of the invention include trichloroethylene, perchloroethylene, l l l :Trichloroethane, carbon tetrachloride, chloroform, monochlorobenzene and l :2 4-trichlor0benzene.
• Dyestuffs which may be incorporated in the emulsions of the invention include any of the well-known classes, for example acid, basic, direct, reactive or disperse dyestuffs as conventionally employed for the dyeing of textile materials composed of polyamide, cotton, wool, silk, acetate, polyester, viscose or acrylic fibres or filaments.
• Textile finishing agents which may be incorporated in the emulsions of the invention include fluorescent optical brightening agents, such as the sodium salts of bis-triazinyl-aminostilbene di-sulphonic acids, waterproofing agents such as stearamidomethylpyridinium chloride and N-methylolstearamide, crease-resist resins such as dimethyloldihydroxy-ethylene urea, antistatic and antisoil/soil release agents such as condensates of ethylene oxide with polyamides, crystallisable polyesters containing polyoxyalkylene groups, for example polyoxyalkylene terephthalate/polyalkylene terephthalate block copolymers and copolymers of polymerisable acids, for example acrylic acid, with other polymerisable vinyl monomers, softening agents such as fatty quaternary ammonium salts, desizing agents such as enzyme preparations, flameproofing or flame retarding agents such as antimony trioxide or mixtures of boric acid and borax.
• the emulsions of the present invention may be produced by subjecting a'mixture' of a halogenated hydrocarbon solvent and an aqueous solution or dispersion of a dyestuff of textile finishing agent to suitable mechanical agitation in the presence of ethyl hydroxyethyl cellulose and at least one anionicsurface-active agent.
• The'emulsifying agents used that is to say the ethyl hydroxyethyl cellulose and the anionic'agent or agents, maybe initially present in either the halogenated hydrocarbon solvent or the aqueous solution or dispersion of the dyestuff or finishing agent, or both.
• the solubility properties of ethyl hydroxyethylcellulose inparticular the 20 35 cp. I grade which is preferred for use in-the present invention, it will usually be convenient for this constituent to be dissolved initially in-the halogenated hydrocarbon solvent.
• the anionic agent or agents may be dissolved initially in either the solvent phase or the aqueous phase, but if desired, in accordance with a well-known technique of emulsification using such agents, it may be produced in situ by reaction between a suitable organic acid precursor, for example dodecylbenzene-sulphonic acid, dissolved in the halogenated hydrocarbon solvent phase and an alkali, for example sodium hydroxide, dissolved in the aqueous phase.
• a suitable organic acid precursor for example dodecylbenzene-sulphonic acid
• an alkali for example sodium hydroxide
• the relative proportions of the halogenated hydrocarbon solvent and the aqueous phase incorporated in i the emulsions of the invention may vary widely, according to the manner in which the emulsions are to be applied to the textile fabric and to the type and solubility of the dyestuffs or finishing agents employed. Commonly, however, the amount of water will lie in the range 0.3 to 20.0% of the total weight of the emulsion.
• the emulsions of the present invention are valuable for the application to textile materials of the dyestuffs or finishing agents which they contain.
• the emulsions may be applied to the textile materials by passing, exhaustion or any other conventional form of impregnation, followed by evaporation of the halogenated hydrocarbon solvent and, if necessary, a final baking operation to fix the dyestuff or finishing agent on the textile material.
• the halogenated hydrocarbon solvent which is evaporated during this process may, of course, be recovered for re-use.
• Textile materials to which the emulsions of the invention may be applied include yarns and knitted, woven or non-woven fabrics.
• emulsions of the invention instead of conventional aqueous solutions or dispersions of dyestuffs or textile finishing agents confers a number of advantages. Exhaustion may be more rapid in batchwise processes and wetting out easier and pick-up better in padding procedures. Losses in dimensional stability are reduced.
• the halogenated hydrocarbon solvents have lower specific heats and latent heats of evaporation than water, thus reducing costs of heating and drying and also permitting economic recovery of the organic liquid for reuse which avoids the increasingly severe difficulties being met in the treatment of aqueous effluents.
• a number of finishing treatments, and also dry cleaning of textile materials are carried out in nonaqueous media and in suitable cases these may be combined with application of a treating agent to the textile material.
• emulsions of the invention show no detectable separation of the organic and aqueous phases over a period of. several days.
• emulsions of similar composition but containing only the ethyl hydroxyethyl cellulose' as stabiliser, that is to say omitting the anionic surface active agent or agents show appreciable separation after as little as one day.
• Example 1 0.70 Part of the dyestuff which is the disodium salt of 2-[2'-acetylamino-4-(4 -chloro-6 '-amino-1 :3" 5 -triazine-2 -ylamino)phenylazo naphthalene-4: 8- disulphonic acid and 022 part of soda ash are dissolved in 13.3 parts of water, and 1.5 parts of Turkey Red Oil isthen added and stirred until in solution.
• the dyestuff which is the disodium salt of 2-[2'-acetylamino-4-(4 -chloro-6 '-amino-1 :3" 5 -triazine-2 -ylamino)phenylazo naphthalene-4: 8- disulphonic acid and 022 part of soda ash are dissolved in 13.3 parts of water, and 1.5 parts of Turkey Red Oil isthen added and stirred until in solution.
• a sample of cellulosic textile material is padded in the emulsion, dried and baked at 200 C for 1 minute.
• the textile material is thereby evenly dyed a yellow colour.
• Example 2 The procedure of Example 1 is repeated, except that in place of the dyestuff there described there is. used 1.1parts of the dyestuff which is the tri-sodium salt of copper phthalocyanine-3-(sulphonic acid):;-3 ⁇ N- [,8-6 chloro-4'-methoxyl :3 15-triazin-2-ylamino)ethyl sulphonamide ⁇ .
• Example 3 The procedure of Example 1 is repeated, except that is place of. the dyestuff there described there is used 0.75 part of the dyestuff which is the tetrasodium salt of 1- ⁇ 2:5-dimethyl-4-[4"-(4-chloro- 6"-amino-l 23135;" triazin-2-ylamino)7-sulphonaphth- 1 -ylazo]phenylazo ⁇ naphthalene-2 5 .7-trisulphonic acid.
• Example 4 The procedure described in Example 1 is repeated, except that the perchloroethylene is replaced by an equal weight of 1 1 l-trichloroethane. An emulsion of excellent stability is again obtained.
• Example 5 The procedure described in Example 1 is repeated,
• Example 7 i 0.05 part of the dyestuff which is the pentasodium salt of 1-(2'-methyl-3-[4-chloro-6"-sulphoanilino- 1" :3 :5 -triazin-2"-ylamino]-5 '-sulphophenyl) -3- carboxy-4-[2"-sulpho-4 -(chlor'osulphoanilino-1 3" :5-triazin-2"-ylamino)phenylazo]-5-pyrazolone and 1.1 parts of urea are dissolved in 1.9 parts of water; 0.145 part of a 45% aqueous solution of the sodium salt of sulphated methyl oleate and 0.26 part of sodium dodecylbenzene sulphonate are then stirred in until dissolved.
• the dyestuff which is the pentasodium salt of 1-(2'-methyl-3-[4-chloro-6"-sulphoanilin
• Cellulosic textile material is batchwise dyed a yellow colour by immersion in a dyebath consisting of the above-described emulsion which is continuously agitated and gradually heated to boiling point,.then maintained at the boil for minutes.
• Example 8 0.036 Part of the dyestuff identified in the Colour Index as C.l. Acid Yellow 72 is dissolved in 0.6 part of water, and 0.145 part of a 45% aqueous solution of the sodium salt of sulphated methyl oleate is added.
• the dyestuff solution so obtained is added with good agitation to a solution of 0.025 part of ethyl hydroxyethyl cellulose of viscosity 2035 cp. in IS parts of perchloroethylene; the emulsion so formed is added with stirring to 149 parts of perchloroethylene at 30 C, to yield a stable product.
• the resulting emulsion is used for the batchwise dye ing of nylon textile materials to a yellow colour by immersing the textile material in the emulsion when maintained at 85 C, at which temperature a clear solution is formed.
• Example 9 The pro cedure of Example 8 is place of the dyestuff there described 0.016 part of the dyestuff which is identified in the Colour Index as C.l. Acid Red 266. A similar result is obtained.
• Example 10 The procedure of Example 8 is repeated, using in place of the dyestuff there described 0.015 part of the dyestuff 4-[4-(phenylazo)phenylazo] N-ethy1-N-(msulphobenzyl)aniline. A similar result is obtained.
• Example 11 0.02 Part of the dyestuff identified in the Colour Index as C.l. Acid Blue 67 is dissolved in 0.6 part of water, and 0.045 part of dodecylbenzene sulphonic acid added.
• the solution so obtained is added with good agitation to a solution of 0.025 parts of ethyl hydroxyethyl cellulose of viscosity 20-35cp, in 15 parts of perchloroethylene; the emulsion so formedis added with stirring to a further 145 parts of perchloroethylene at 30 C.
• the resultant dye liquor is employed for the batchwise dyeing of nylon textile material according to the following procedure
• Perchloroethylene is circulated through the nylon textile material at 40 C for 10 minutes; the dye liquor in an amount sufficient to deposit from 1.25 to 1.5 by weight of the dyestuff (based on the textile material taken), is then circulated through the material so treated at'40 C for 15 minutes, after which the temperature is raised to 85 C over a period of 40 minutes and then maintained at that value for 15 minutes.
• the material is dried at 70-80 C.
• Example 12 repeated, using in The procedure of Example 11 is repeated, using in place of the dyestuff there identified 0.016 part of the dyestuff referred to in Example 10. A similar result to that described in Example 1 1 is obtained.
• Example 13 Thqprocedure of Example 11 is repeated, using in place of the dyestuff there identifed 0.037 part of the dyestuff identified in the Colour Index as C.l. Acid Yellow 135. A similar result is obtained.
• Example 14 The procedure of Exa mple 11 is repeated, using in place of the dyestuff there identified 0.017 part of the dyestuff identified in the Colour Index as C.l. Acid Blue 40. A similar result is obtained.
• Example 15 The procedure of Example 11 is repeated, using in place of the dyestuff there identified 0.036 part of the dyestuff identified in the Colour index as C.l. Acid Yellow 72. A similar result is obtained.
• Example 16 1 part of Turkey Red Oil is dissolved in 30 parts of an 18 solution in aqueous diethylene glycol of a fluorescent brightening agent which is an anionic stilbene derivative; this solution is added to a solution of 5 parts of ethyl hydroxyethyl cellulose, viscosity 20 35 cp., in 70 parts of per chloroethylene, whilst the latter is agitated with a Silverson homogeniser. Agitation is continued for 1 minute after the addition'is complete.
• the resultant emulsion is viscous but pourable, and has excellent stability. It is suitable for the optical bleaching of cellulosic of polyamide fabrics and for this purpose it may be diluted with additional perchloroethylene without breakage of the emulsion occurring.
• the diluted emulsion is padded on to a cellulosic fabric so as to deposit 0.05-0.5% by weight of the fluorescent brightening agent on the fabric; the solvent is then removed by passing the fabric through a steam chamber and the fabric is dried at C for 5 minutes' The treated fabric is considerably brighter in appearance than the untreated fabric.
• Example 17 v I '1 part of Turkey Red Oil is dissolved in 30 parts of a 50 aqueous solution of dimethyloldihydroxyethy lene urea and is added to a solution of 1.5 parts of ethyl hydroxyethyl cellulose, viscosity 2035 cp., in parts of perchloroethylene whilst the latter is agitated with a Silverson homogeniser. Agitation is continued for 1 minute after the addition is complete.
• the resultant emulsion which is viscous but pourable, has excellent stability. It is suitable for application together with a latent acid catalyst to cellulosic and'polyester/cellulosic fabrics for the production of crease-resist and durable press finishes, and for. this purpose it may be diluted with additional perchloroethylene without the emulsion breaking.
• a latent acid catalystsu'ch as monochloroacetic acid or stearamidomethylpyridinium chloride is added to the diluted perchloroethylene emulsion and the resulting composition is'padded on to cellulosic or polyester-cellulosic blend fabric so as to deposit 4 8 by weight of the dimethylol dihydroxyethylene urea on the fabric.
• the solvent is then removed by passing the fabric through a steam chamher, the fabric is thereafter'dried at 60 C for 5 minutes and then heated at a temperature of C for 3 minutes.
• the treated fabric possesses much improved wet and dry crease recovery properties compared with the untreated fabric.
• Example 18 0.4 part of sodium hydroxide is dissolved in 50 parts of a 15 w/v. aqueous dispersion of a polyethylene terephthalate/polyoxyethylene terephthalate block copolymer; 2 parts of ethyl hydroxyethyl cellulose, viscosity 20 35 cp., are dissolved in 45 parts of perchloroethylene, followed by 2.6 parts of oleic acid.
• the aqueous dispersion is added over a period of minutes to the oil phase, using a high-speed stirrer; after the addition is completed, stirring is continued at high speed for 3 minutes, followed by slow-speed stirring for 2 minutes.
• the resulting emulsion has excellent stability and is suitable for conferring durable antistatic and anti-soil effects on polyester, polyester/cellulosic and polyester/wool blend fabrics; it may be diluted for this pur pose with additional perchloroethylene without the emulsion breaking.
• the diluted emulsion is padded on to polyester fabric so as to deposit 1 3 by weight of the polyethylene terephthalate/polyoxyethylene terephthalate block copolymer on to the fabric.
• the fabric is dried by heating at 70 C for 20 minutes.
• the treated fabric is found to possess superior antisoil-redeposition, stain release and antisoil properties to the untreated fabric.
• Example 19 0.2 Part of an azo dye, prepared by coupling 4- aminobenzene sulphona mide on to N-methyl-N-B- cyanoethyl aniline, and 0.1 part of the polyurea deflocculating agent obtained as described below from mixed 2,4- and 2,6-tolylene diisocyanates and afatty secondary amine derived from soya are gravel milled in 3 parts of perchloroethylene for 40 hours. The resulting dispersion is added with stirring to a solution of 1 part ethyl hydroxyethyl cellulose of viscosity 20-35 cp (measured at 25 C on a 5 by weight solution in 80:20 toluene/ethanol) dissolved in 115 parts perchloroethylene.
• an azo dye prepared by coupling 4- aminobenzene sulphona mide on to N-methyl-N-B- cyanoethyl aniline, and 0.1 part of the polyurea deflocculating agent obtained as described below from
• a mixture of 5 parts of water and 1 part of cially available 40 solution in butyl acetate of polymerised mixed 2,4- and 2,6-tolylene diisocyanates con taining 5.7 of isocyanate groups and less than 0.5 of free tolylene diisocyanate is gradually added to a stirred solution in 1 18 parts of acetone at 50-55 C of 53.5 parts of a fatty secondary amine derived from soya, commercially available under the trade name Armeen 2S (Armeen is a Registered Trade Mark).
• Armeen 2S Armeen is a Registered Trade Mark
• Example 20 0.5 Parts of the dye identified in the Colour Index as Cl Basic Red 18 is dissolved in 5 parts boiling water and 5 parts Turkey Red Oil are added. The dye solution so obtained is added with good agitation to a solution of 1 part of ethyl hydroxyethyl cellulose o f 20-35 cp. in 115 parts perchloroethylene and the emulsion so formed is diluted with stirring with 687 parts perchloroethylene.
• the resulting emulsion is used for the batchwise dyeing of polyacrylonitrile textile materials to a red colour by immersing the textile material in the emulsion for 30 minutes at C in a closed vessel with continuous agitation.
• emulsifying agents as ethyl hydroxyethyl cellulose having a solution viscosity, measured on a 5% solution by weightin 80:20 (by weight) toluene/ethanol of from 20 to 35 cp, and at least one anionic surface-active agent, the amount of water present in said emulsion being from 0.3 to 20% of the total weight of the emulsion.
• a process for the treatment of textile materials in which there is applied to the textile material a stabilised emulsion as claimed in claim 1 and the material is thereafter treated in known manner to fix the treatment agent thereupon.

Landscapes

• Engineering & Computer Science (AREA)
• Textile Engineering (AREA)
• Chemical & Material Sciences (AREA)
• Dispersion Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Molecular Biology (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
• Coloring (AREA)

Applications Claiming Priority (1)

Publications (1)

Family

ID=10165958

Family Applications (1)

Country Status (9)

Cited By (13)

Families Citing this family (1)

Citations (5)

• 1970
  • 1970-05-05 GB GB2161870A patent/GB1315843A/en not_active Expired
• 1971
  • 1971-04-30 US US00139275A patent/US3771955A/en not_active Expired - Lifetime
  • 1971-05-04 AU AU28475/71A patent/AU2847571A/en not_active Expired
  • 1971-05-04 NL NL7106060A patent/NL7106060A/xx unknown
  • 1971-05-04 FR FR7116096A patent/FR2091207A5/fr not_active Expired
  • 1971-05-04 CA CA112,151A patent/CA941710A/en not_active Expired
  • 1971-05-05 BE BE766769A patent/BE766769A/xx unknown
  • 1971-05-05 CH CH662371D patent/CH662371A4/xx unknown
  • 1971-05-05 CH CH662371A patent/CH553878A/xx unknown
  • 1971-05-05 DE DE19712122264 patent/DE2122264A1/de active Pending

Patent Citations (5)

Also Published As

Similar Documents