US2974065A - Process for reducing the luster of textile materials - Google Patents
Process for reducing the luster of textile materials Download PDFInfo
- Publication number
- US2974065A US2974065A US69061557A US2974065A US 2974065 A US2974065 A US 2974065A US 69061557 A US69061557 A US 69061557A US 2974065 A US2974065 A US 2974065A
- Authority
- US
- United States
- Prior art keywords
- acid
- melamine
- textile materials
- formaldehyde
- lustre
- 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
- 239000000463 material Substances 0.000 title claims description 53
- 238000000034 method Methods 0.000 title claims description 28
- 239000004753 textile Substances 0.000 title claims description 23
- 239000002932 luster Substances 0.000 title description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 30
- 239000002253 acid Substances 0.000 claims description 24
- 229920000877 Melamine resin Polymers 0.000 claims description 14
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 14
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 11
- 239000007864 aqueous solution Substances 0.000 claims description 11
- 239000007859 condensation product Substances 0.000 claims description 11
- 238000010438 heat treatment Methods 0.000 claims description 11
- 239000002270 dispersing agent Substances 0.000 claims description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 8
- 150000007513 acids Chemical class 0.000 claims description 8
- 238000010494 dissociation reaction Methods 0.000 claims description 6
- 230000005593 dissociations Effects 0.000 claims description 6
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 6
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 238000004326 stimulated echo acquisition mode for imaging Methods 0.000 claims 1
- 239000004744 fabric Substances 0.000 description 23
- 229920002301 cellulose acetate Polymers 0.000 description 15
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 14
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 14
- 239000000243 solution Substances 0.000 description 10
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 9
- -1 aliphatic hydroxy carboxylic acids Chemical class 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 150000004665 fatty acids Chemical class 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 239000003599 detergent Substances 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- 238000005470 impregnation Methods 0.000 description 4
- 239000008149 soap solution Substances 0.000 description 4
- 238000010025 steaming Methods 0.000 description 4
- 239000011975 tartaric acid Substances 0.000 description 4
- 235000002906 tartaric acid Nutrition 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229920002302 Nylon 6,6 Polymers 0.000 description 3
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 3
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- 239000005696 Diammonium phosphate Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000005639 Lauric acid Substances 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 2
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 2
- 235000019838 diammonium phosphate Nutrition 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- MWZFQMUXPSUDJQ-KVVVOXFISA-M sodium;[(z)-octadec-9-enyl] sulfate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCCOS([O-])(=O)=O MWZFQMUXPSUDJQ-KVVVOXFISA-M 0.000 description 2
- 239000011550 stock solution Substances 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- 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
- KJWMCPYEODZESQ-UHFFFAOYSA-N 4-Dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=C(O)C=C1 KJWMCPYEODZESQ-UHFFFAOYSA-N 0.000 description 1
- CYYZDBDROVLTJU-UHFFFAOYSA-N 4-n-Butylphenol Chemical compound CCCCC1=CC=C(O)C=C1 CYYZDBDROVLTJU-UHFFFAOYSA-N 0.000 description 1
- PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical class NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N Arginine Chemical compound OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 239000004141 Sodium laurylsulphate Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Chemical group 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical compound NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000000549 coloured material Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- ALBYIUDWACNRRB-UHFFFAOYSA-N hexanamide Chemical compound CCCCCC(N)=O ALBYIUDWACNRRB-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229940033355 lauric acid Drugs 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000001301 oxygen Chemical group 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 239000012262 resinous product Substances 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Images
Classifications
-
- 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/423—Amino-aldehyde resins
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2861—Coated or impregnated synthetic organic fiber fabric
- Y10T442/2869—Coated or impregnated regenerated cellulose fiber fabric
Definitions
- PROCESS FOR REDUCING THE LUSTER OF TEXTILE MATERIALS Filed Oct. 17, 1957 PREPARING AQUEOUS MELAMINE/FORMALDEHYDE SOLUTION CONTAINING ACID CATALYST AND NON-'IONIC DISPERSING AG NT PRODUCING TEXTILE FABRIC PADDING FABRIC WITH SOLUTION STEAMING SCOURING DRYING United States Pat ent-O PROCESS FOR REDUCING THE LUSTER OF TEXTILE MATERIALS Ralph James Mann and Jozef Biedawski, Spondon, near Derby, England, assignors to British Celanese Limited, a corporation of Great Britain Filed Oct. 17, 1957, Ser. No. 690,615
- This invention relates to effecting a reduction of the lustre of textile materials, particularly fabrics, especially those of cellulose acetate or other cellulose esters of lower fatty acids.
- the reduction of lustre of textile materials is effected by uniformly impregnating the material with an aqueous solution of a water-soluble condensation product of melamine and formaldehyde (eg a methylol melamine) the solution containing an acid, particularly a strong organic acid, together with a non-ionic dispersing agent, and then while the material is so impregnated heating it in an atmosphere such that the material remains wet.
- the acid acts as a catalyst to promote the formation of a white amorphous product from the condensate.
- the drawing is a flow sheet of one embodiment of the process of this invention.
- the acid employed is preferably of low volatility and advantageously a strong aliphatic carboxylic acid of low volatility; we have obtained particularly good results by the use of aliphatic hydroxy carboxylic acids containing at least two carboxylic groups.
- the acid is preferably one having a dissociation constant of at least l 10 Examples of such acids are citric acid, tartaric acid and lactic acid. All these acids have dissociation constants below 1 10 but stronger acids of low volatility may be used e.g. acids ranging in strength up to that of phosphoric acid and oxalic acid which have dissociation constants of, about 1 10- and 6.5 l-
- the concentration of the citric or other acid in the aqueous solution may be from 0.54%, for example 1-2%.
- salts thereof with volatile bases e.g. ammonia or methyl amine may be employed.
- diammonium phosphate or oxalate or ammonium salts of citric or tartaric acid may be employed.
- the non-ionic dispersing agent may be one obtainable by condensing ethylene oxide with (a) a fatty acid containing a chain of at least 10 carbon atoms starting from and including the carbon atoms of the carboxyl group,
- a fatty alcohol containing a chain of at least 10 carbon atoms starting from and including the carbon atom carrying the hydroxyl group e.g. lauryl alcohol, cetyl alcohol or oleyl alcohol, or with an alkyl phenol in which the alkyl group contains a chain of at least 4 carbon atoms starting from and including the one directly attached to the benzene ring, e.g. p-n-dodecyl-phenol or p-n-butylphenol.
- the number of molecules of ethylene oxide per molecule of fatty acid, fatty alcohol, or alkyl-phenol must be sufficient to yield a water-soluble product, for example from 15 to 25 molecules.
- Commercial products of these kinds are Pentrosan A2 sold by Glovers (Chemicals) Ltd., and Dispersol VL sold by Imperial Chemical Industries Ltd., a fatty alcohol/ethylene oxide condensate.
- the temperature at which the heating is effected may be from 50 to C. Heating while maintaining the material in the wet state can be effected by heating in air saturated with water vapour, or in saturated steam,
- the latter is passed continuously through a substantially closed chamber into which steam is injected to bring the atmosphere to the required temperature.
- the chamber may be provided with a series of upper rollers and a series of lower rollers over and under which the fabric passes as in certain types of steamer employed for the steaming'of prints on textile materials.
- the impregnation liquor contains a salt of the acid with a volatile base it is desirable that provision be made for removing volatile base from the neighbourhood of the fabric, as by permitting steam to escape from the steaming chamber-so carry away volatile base.
- the Water-soluble melamine/formaldehyde condensation product may be one made by reaction of 1 molecular proportion of melamine with from 1-6 molecular proportions, particularly 3-6 molecular proportions, 1 of formaldehyde.
- the melamine may be warmed with .the required proportion of aqueous formaldehyde of 30-40% strength, until the melamine is dissolved.
- Such a condensation product may be diluted with water 'to.' .a strength suitable for application to the material.
- the acid is added together with the non-ionic dispersing agent.
- concentrations corresponding with down to 0.5% of melamine may be used according to the effect desired, e.g. concentrations corresponding with down to 0.5% of melamine.
- the proportion of melamine/ formaldehyde condensate applied to the material may be such as corresponds to from 4 to 12% of melamine, particularly 4 to 8%, based on the weight of the textile material. Smaller proportions may be used however, depending on the reduction of lustre required, for example proportions down to that corresponding with 0.5 of melamine.
- salts thereof with volatile bases e.g. ammonia or methyl amine may be employed.
- diammonium phosphate or oxalate or ammonium salts of critric or tartaric acid may be employed.
- the impregnation of the textile material with the aqueous acid solution of the melamine/formaldehyde condensate may be effected by padding.
- a fabric may be padded with the solution by means of a padding mangle, the latter being adjusted so as to leave in the material from 50-100% of its weight of the solution based on the weight of the material.
- the melamine/formaldehyde condensates maybe replaced, though usually With less satisfaction, by similar water-soluble condensation products of formaldehyde with urea, thiourea, or ethylene-urea our-NH o o onT-NH or another substance including the grouping (where X is nitrogen, oxygen or sulphur) and capable of reacting with formaldehyde to form a water-soluble product containing at least two methylol groups attached to nitrogen.
- the new delustn'ng process may be applied to textile fabrics and other materials of acetone-soluble cellulose acetate. In this way there may be obtained, with a high degree of reproducibility, products of reduced lustre which are resistant to repeated washing with a soap solution at 60 C. Moreover the resultant low lustre material does not re-lustre when ironed wet as is the case with acetone-soluble cellulose acetate fabrics which have been delustred by boiling in hot soap solutions. Again the new process may be very satisfactorily employed to effect reduction of lustre of textile materials of cellulose acetate or other cellulose esters of lower fatty acids, the said esters containing not more than 0.29 alcoholic hydroxyl groups per C unit of the cellulose molecule.
- the process may be applied to textile fabrics or other textile materials of cellulose acetate of acetyl value at least 59%, e.g. 60.5-62.5% calculated as acetic acid.
- Such materials cannot be delustred by the simple expedient of boiling with hot soap solutions as is the case with materials of acetone-soluble cellulose acetate.
- the new process may be applied to uncoloured materials or to already coloured materials as may be desired.
- Textile materials of other cellulose esters of lower fatty acids which may be treated include those of cellulose propionate, cellulose acetate propionate and cellulose acetate butyrate.
- Textile materials other than those of cellulose esters which may be treated by the process of the invention include those of regenerated cellulose and thoseof wholly synthetic linear polymers, for example of polyamides, e.g. polyhexamethylene adipamide (nylon 66) or poly-caproamide (nylon 6'), or of polyesters, e.g. polyethylene-terephthalate.
- polyamides e.g. polyhexamethylene adipamide (nylon 66) or poly-caproamide (nylon 6')
- polyesters e.g. polyethylene-terephthalate.
- Textile materials which have been treated by the new process may subsequently be scoured in an aqueous solution of a detergent in order to remove acid and any loosely adherent condensation product.
- the detergent may be anionic for example a long chain fatty alcohol sulphate e.g. sodium oleyl sulphate or sodium lauryl sulphate, or an alkylarylsulphonate, e.g. sodium dodecylbenzenesulphonate.
- a stock solution of melamine/formaldehyde condensate is prepared by Warming 48 parts by weight of melamine with 180 parts by weight of commercial aqueous formaldehyde of 36-40% strength until the mixture is clear.
- a padding solution is prepared of the following compositions:
- Non-ionic dispersing agent may be Pentrosan A2 (Glovers) or Dispersol VL (I.C.I.) or a product containing about 35% of active ingredient made by condensing one molecular proportion of lauric acid or oleyl or cetyl alcohol with about 20 molecular proportions of ethylene oxide.
- a plain satin fabric or crepe satin fabric of acetonesoluble cellulose acetate is padded with the foregoing solution on a padding mangle adjusted to leave the fabric containing about 80% of its weight of the padding liquor.
- the fabric is then, while still wet, run as a series of loops through a chamber into which steam is injected so as to give a temperature within the chamber of about 80 C.
- the duration of the passage of the fabric is from 4-9 minutes.
- the fabric may be scoured, for example with an aqueous bath containing an anionic or non-ionic detergent.
- the material may be scoured for 3 to 5 minutes at a temperature of 60 C. using a 2 to 5 grams per litre aqueous solution of Perlankrol C27, an anionic detergent sold by Lankro Chemical Co. Ltd. or a l to 2 grams per litre aqueous solution of sodium oleyl sulphate.
- the resulting fabrics are of uniformly low lustre which is substantially unaltered by six washings in a 2 g./l. soap solution at 60 C., or by dry-cleaning with white spirit, perchloroethylene or trichloroethylene, and do not re-lustre on ironing in the wet state with a hot iron. They have a pleasant, soft but weighty handle.
- Either of the fabrics may subsequently be dyed with disperse dyes in level shades, for example in shades of pale to medium depth.
- the process described in the foregoing example may be applied with similar results to fabrics of continuous filament yarns of cellulose acetate of acetyl value 61%, calculated as acetieacirl, such as may be obtained by dry-spinning a solution of the cellulose acetate in a mixture of methylene chloride and methyl alcohol in the proportion of 93 to 7 by weight. Again it may be applied to a fabric of yarns of (nylon 66) or (nylon 6).
- a process according to claim '5 wherein the impregnated material carries an amount of a melamine/ formaldehyde condensation product equivalent to from 4 to 8% of melamine based on the weight of the material and the acid is present to the extent of 1 to 2 percent based on the weight of the impregnation solution.
- a process according to claim 5, wherein the textile material is a fabric of cellulose acetate of acetyl value from 60 to 62.5% calculated as acetic acid.
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- Chemical & Material Sciences (AREA)
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Description
March 7, 1961 R. J. MANN ETAL 2,974,065
PROCESS FOR REDUCING THE LUSTER OF TEXTILE MATERIALS Filed Oct. 17, 1957 PREPARING AQUEOUS MELAMINE/FORMALDEHYDE SOLUTION CONTAINING ACID CATALYST AND NON-'IONIC DISPERSING AG NT PRODUCING TEXTILE FABRIC PADDING FABRIC WITH SOLUTION STEAMING SCOURING DRYING United States Pat ent-O PROCESS FOR REDUCING THE LUSTER OF TEXTILE MATERIALS Ralph James Mann and Jozef Biedawski, Spondon, near Derby, England, assignors to British Celanese Limited, a corporation of Great Britain Filed Oct. 17, 1957, Ser. No. 690,615
Claims priority, application Great Britain Nov. 1, 1956 I 10 Claims. (Cl. 117-1193) This invention relates to effecting a reduction of the lustre of textile materials, particularly fabrics, especially those of cellulose acetate or other cellulose esters of lower fatty acids.
It is well known that the lustre of lustrous textile materials can be reduced by forming on the material, or in the presence of the material, particles of amorphous water-insoluble condensation products of formaldehyde with urea or melamine. Such processes are described in British patent specifications 467,480, 469,688 and 568,- 438. In applying such processes to fabrics of cellulose acetate we have found that the procedures specifically recommended suffer from various defects from a commercial point of view. For instance, we have found it very difiicult to obtain consistently a reduction of lustre sufliciently uniform for commercial purposes and to obtain consistently a given reduction of lustre.
We have now found a new method whereby these dif-' ficulties may be avoided and reduction of lustre effected with a'high degree of uniformity and reproducibility. According to our new process, the reduction of lustre of textile materials, especially those of cellulose acetate or other cellulose esters and lower fatty acids, is effected by uniformly impregnating the material with an aqueous solution of a water-soluble condensation product of melamine and formaldehyde (eg a methylol melamine) the solution containing an acid, particularly a strong organic acid, together with a non-ionic dispersing agent, and then while the material is so impregnated heating it in an atmosphere such that the material remains wet. The acid acts as a catalyst to promote the formation of a white amorphous product from the condensate.
The drawing is a flow sheet of one embodiment of the process of this invention.
The acid employed is preferably of low volatility and advantageously a strong aliphatic carboxylic acid of low volatility; we have obtained particularly good results by the use of aliphatic hydroxy carboxylic acids containing at least two carboxylic groups. The acid is preferably one having a dissociation constant of at least l 10 Examples of such acids are citric acid, tartaric acid and lactic acid. All these acids have dissociation constants below 1 10 but stronger acids of low volatility may be used e.g. acids ranging in strength up to that of phosphoric acid and oxalic acid which have dissociation constants of, about 1 10- and 6.5 l-
' respectively. Very good results can be obtained with citric acid. The concentration of the citric or other acid in the aqueous solution may be from 0.54%, for example 1-2%.
In place of the free acids salts thereof with volatile bases e.g. ammonia or methyl amine may be employed. Thus we may use diammonium phosphate or oxalate or ammonium salts of citric or tartaric acid. When the impregnated-material is heated they dissociate with for- .mation of free acid.
As already indicated the aqueous impregnation liquor ..contains a, non-ionic dispersingagentw This. is a very ice Patented Mar. 7, 1961 washed from the material and impart a glitter to the lat- Again, if a cationic dispersing agent is employed ter. the delustre effect is not sufficiently resistant to washing.
The non-ionic dispersing agent may be one obtainable by condensing ethylene oxide with (a) a fatty acid containing a chain of at least 10 carbon atoms starting from and including the carbon atoms of the carboxyl group,
.e.g. lauric acid, palmitic acid, or oleic acid, or with (b) a fatty alcohol containing a chain of at least 10 carbon atoms starting from and including the carbon atom carrying the hydroxyl group, e.g. lauryl alcohol, cetyl alcohol or oleyl alcohol, or with an alkyl phenol in which the alkyl group contains a chain of at least 4 carbon atoms starting from and including the one directly attached to the benzene ring, e.g. p-n-dodecyl-phenol or p-n-butylphenol. The number of molecules of ethylene oxide per molecule of fatty acid, fatty alcohol, or alkyl-phenol must be sufficient to yield a water-soluble product, for example from 15 to 25 molecules. Commercial products of these kinds 'are Pentrosan A2 sold by Glovers (Chemicals) Ltd., and Dispersol VL sold by Imperial Chemical Industries Ltd., a fatty alcohol/ethylene oxide condensate.
The temperature at which the heating is effected may be from 50 to C. Heating while maintaining the material in the wet state can be effected by heating in air saturated with water vapour, or in saturated steam,
that is in a saturated water vapour atmosphere. .The
fected with a heating time in the range of 2-15 minutes.
Conveniently, in the case of a fabric, the latter is passed continuously through a substantially closed chamber into which steam is injected to bring the atmosphere to the required temperature. To provide conveniently for the requisite time of passage coupled with a reasonable linear speed of passage the chamber may be provided with a series of upper rollers and a series of lower rollers over and under which the fabric passes as in certain types of steamer employed for the steaming'of prints on textile materials. When the impregnation liquor contains a salt of the acid with a volatile base it is desirable that provision be made for removing volatile base from the neighbourhood of the fabric, as by permitting steam to escape from the steaming chamber-so carry away volatile base.
It is very important that the material be not allowed a to become dry during the heating treatment. If itbecomesdry there is a tendency for the melamine/formaldehyde condensation product to be converted intora resinous product having little'effect on the lustre of material.
The Water-soluble melamine/formaldehyde condensation product may be one made by reaction of 1 molecular proportion of melamine with from 1-6 molecular proportions, particularly 3-6 molecular proportions, 1 of formaldehyde. The melamine may be warmed with .the required proportion of aqueous formaldehyde of 30-40% strength, until the melamine is dissolved. Such a condensation product may be diluted with water 'to.' .a strength suitable for application to the material. Before application of the condensate solution to the. material the acid is added together with the non-ionic dispersing agent.
the
concentration corresponding with 4 to 8% of melamine,
but lower concentrations may be used according to the effect desired, e.g. concentrations corresponding with down to 0.5% of melamine.
The proportion of melamine/ formaldehyde condensate applied to the material may be such as corresponds to from 4 to 12% of melamine, particularly 4 to 8%, based on the weight of the textile material. Smaller proportions may be used however, depending on the reduction of lustre required, for example proportions down to that corresponding with 0.5 of melamine.
In place of the free acids salts thereof with volatile bases e.g. ammonia or methyl amine may be employed. Thus we may use diammonium phosphate or oxalate or ammonium salts of critric or tartaric acid. When the impregnated material is heated they dissociate with formation of free acid.
The impregnation of the textile material with the aqueous acid solution of the melamine/formaldehyde condensate, may be effected by padding. Thus a fabric may be padded with the solution by means of a padding mangle, the latter being adjusted so as to leave in the material from 50-100% of its weight of the solution based on the weight of the material.
The melamine/formaldehyde condensates maybe replaced, though usually With less satisfaction, by similar water-soluble condensation products of formaldehyde with urea, thiourea, or ethylene-urea our-NH o o onT-NH or another substance including the grouping (where X is nitrogen, oxygen or sulphur) and capable of reacting with formaldehyde to form a water-soluble product containing at least two methylol groups attached to nitrogen.
The new delustn'ng process may be applied to textile fabrics and other materials of acetone-soluble cellulose acetate. In this way there may be obtained, with a high degree of reproducibility, products of reduced lustre which are resistant to repeated washing with a soap solution at 60 C. Moreover the resultant low lustre material does not re-lustre when ironed wet as is the case with acetone-soluble cellulose acetate fabrics which have been delustred by boiling in hot soap solutions. Again the new process may be very satisfactorily employed to effect reduction of lustre of textile materials of cellulose acetate or other cellulose esters of lower fatty acids, the said esters containing not more than 0.29 alcoholic hydroxyl groups per C unit of the cellulose molecule. Thus the process may be applied to textile fabrics or other textile materials of cellulose acetate of acetyl value at least 59%, e.g. 60.5-62.5% calculated as acetic acid. Such materials cannot be delustred by the simple expedient of boiling with hot soap solutions as is the case with materials of acetone-soluble cellulose acetate. The new process may be applied to uncoloured materials or to already coloured materials as may be desired.
As already indicated, the processes are of particular value for textile materials of cellulose acetate. Textile materials of other cellulose esters of lower fatty acids which may be treated include those of cellulose propionate, cellulose acetate propionate and cellulose acetate butyrate.
Textile materials other than those of cellulose esters which may be treated by the process of the invention include those of regenerated cellulose and thoseof wholly synthetic linear polymers, for example of polyamides, e.g. polyhexamethylene adipamide (nylon 66) or poly-caproamide (nylon 6'), or of polyesters, e.g. polyethylene-terephthalate.
Textile materials which have been treated by the new process may subsequently be scoured in an aqueous solution of a detergent in order to remove acid and any loosely adherent condensation product. The detergent may be anionic for example a long chain fatty alcohol sulphate e.g. sodium oleyl sulphate or sodium lauryl sulphate, or an alkylarylsulphonate, e.g. sodium dodecylbenzenesulphonate.
The invention is illustrated by the following example:
A stock solution of melamine/formaldehyde condensate is prepared by Warming 48 parts by weight of melamine with 180 parts by weight of commercial aqueous formaldehyde of 36-40% strength until the mixture is clear.
A padding solution is prepared of the following compositions:
Melamine/formaldehyde stock solution prepared as above ccs Water ccs 120 Citric acid --g 2.5 Non-ionic dispersing agent cc 5 The non-ionic dispersing agent may be Pentrosan A2 (Glovers) or Dispersol VL (I.C.I.) or a product containing about 35% of active ingredient made by condensing one molecular proportion of lauric acid or oleyl or cetyl alcohol with about 20 molecular proportions of ethylene oxide.
A plain satin fabric or crepe satin fabric of acetonesoluble cellulose acetate is padded with the foregoing solution on a padding mangle adjusted to leave the fabric containing about 80% of its weight of the padding liquor. The fabric is then, while still wet, run as a series of loops through a chamber into which steam is injected so as to give a temperature within the chamber of about 80 C. The duration of the passage of the fabric is from 4-9 minutes. After leaving the steaming chamber the fabric may be scoured, for example with an aqueous bath containing an anionic or non-ionic detergent. Thus the material may be scoured for 3 to 5 minutes at a temperature of 60 C. using a 2 to 5 grams per litre aqueous solution of Perlankrol C27, an anionic detergent sold by Lankro Chemical Co. Ltd. or a l to 2 grams per litre aqueous solution of sodium oleyl sulphate.
The resulting fabrics are of uniformly low lustre which is substantially unaltered by six washings in a 2 g./l. soap solution at 60 C., or by dry-cleaning with white spirit, perchloroethylene or trichloroethylene, and do not re-lustre on ironing in the wet state with a hot iron. They have a pleasant, soft but weighty handle.
Either of the fabrics may subsequently be dyed with disperse dyes in level shades, for example in shades of pale to medium depth. The process described in the foregoing example may be applied with similar results to fabrics of continuous filament yarns of cellulose acetate of acetyl value 61%, calculated as acetieacirl, such as may be obtained by dry-spinning a solution of the cellulose acetate in a mixture of methylene chloride and methyl alcohol in the proportion of 93 to 7 by weight. Again it may be applied to a fabric of yarns of (nylon 66) or (nylon 6).
Having described our invention, what we desire to secure by Letters Patent is:
1. In a process for effecting a reduction of the lustre of textile materials which comprises uniformly impreg mating the material with an aqueous solution containing a catalyst selected from the group consisting of acids and salts thereof with ammonia, said acids being sub stautially non-volatile in steam at C. and of dissociation constant at least 1 10- and a water-soluble condensation product of formaldehyde with a compound selected from the group consisting of melamine, urea, ethylene urea, and thiourea and then heating the impregnated material to a temperature of at least 50 C. under such conditions that the material remains wet, the step of including a non-ionic dispersing agent in the aqueous solution.
2. A process according to claim 1, wherein the heating is effected by the action of an atmosphere, saturated with water vapour, at a temperature of 50 to 100 C.
3. A process according to claim 2, wherein the catalyst is an acid and is an aliphatic carboxylic acid which is substantially non-volatile in steam at 100 C.
4. In a process for effecting a reduction of the lustre of textile materials of cellulose acetate which comprises uniformly impregnatingthe material with an aqueous solution containing an aliphatic carboxylic acid, of dissociation constant at least 1X10 which is substantially non-volatile in steam at 100 C. and a water-soluble condensation product of formaldehyde with melamine, and then heating the impregnated material to a temperature of at least 50 C. under such conditions that the material remains wet, the step of including a non-ionic dispersing agent in the aqueous solution.
5. A process according to claim 4, wherein the heating is effected by the action of an atmosphere, saturated with water vapour, at a temperature of 50 to 100 C.
6. A" process according to claim '5, wherein the impregnated material carries an amount of a melamine/ formaldehyde condensation product equivalent to from 4 to 8% of melamine based on the weight of the material and the acid is present to the extent of 1 to 2 percent based on the weight of the impregnation solution.
7. A process according to claim 5, wherein the acid is citric acid.
8. A process according to claim 5, wherein the acid is tartaric acid.
9. A process according to claim 5, wherein the textile material is a fabric of acetone-soluble cellulose acetate.
10. A process according to claim 5, wherein the textile material is a fabric of cellulose acetate of acetyl value from 60 to 62.5% calculated as acetic acid.
References Cited in the ,file of this patent UNITED STATES PATENTS 2,190,672 .Me'harg Feb. 20, 1940 2,709,141 Burks May 24, 1955 2,804,441 Nickerson Aug. 27, 1957 2,844,488 Meharg et a1. July 22, 1958 2,852,479 Bender Sept. 16, 1958 FOREIGN PATENTS 1 499,207 Great Britain June 16, 1939
Claims (1)
1. IN A PROCESS FOR EFFECTING A REDUCTION OF THE LUSTRE OF TEXTILE MATERIALS WHICH COMPRISES UNIFORMLY IMPREGNATING THE MATERIAL WITH AN AQUEOUS SOLUTION CONTAINING A CATALYST SELECTED FROM THE GROUP CONSISTING OF ACIDS AND SALTS THEREOF WITH AMMONIA, SAID ACIDS BEING SUBSTANTIALLY NON-VOLATILE IN STEAM AT 100*C. AND OF DISSOCIATION CONSTANT AT LEAST 1X10-4, AND A WATER-SOLUBLE CONDENSATION PRODUCT OF FORMALDEHYDE WITH A COMPOUND SELECTED FROM THE GROUP CONSISTING OF MELAMINE, UREA, ETHYLENE UREA, AND THIOUREA AND THEN HEATING THE IMPREGNATED MATERIAL TO A TEMPERATURE OF AT LEAST 50*C. UNDER SUCH CONDITIONS THAT THE MATERIAL REMAINS WET, THE STEP OF INCLUDING A NON-IONIC DISPERSING AGENT IN THE AQUEOUS SOLUTION.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3336256A GB865857A (en) | 1956-11-01 | 1956-11-01 | Improvements in the treatment of textile materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2974065A true US2974065A (en) | 1961-03-07 |
Family
ID=10351933
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US69061557 Expired - Lifetime US2974065A (en) | 1956-11-01 | 1957-10-17 | Process for reducing the luster of textile materials |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2974065A (en) |
| GB (1) | GB865857A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3177093A (en) * | 1962-06-06 | 1965-04-06 | American Cyanamid Co | Method of treating cellulose textile material and the treated material |
| US3218119A (en) * | 1962-02-02 | 1965-11-16 | American Cyanamid Co | Method of applying cyclic urea resins to cellulosic textile materials |
| US3242119A (en) * | 1960-03-22 | 1966-03-22 | Ciba Ltd | Water soluble synthetic resin compositions comprising a melamine-formaldehyde condensate and an unoxidized alkyd resin |
| US3890095A (en) * | 1967-04-05 | 1975-06-17 | American Cyanamid Co | Cellulosic textile finish with 1,3-dimethylol-4,5-dihydroxy-2-imidazolidinone, zinc nitrate and a sequestering agent |
| US3916063A (en) * | 1973-10-11 | 1975-10-28 | Thilmany Pulp & Paper Company | Method for manufacturing a printable, glueable polyolefin web material |
| US3950589A (en) * | 1972-03-23 | 1976-04-13 | Toray Industries, Inc. | Melt-resistant synthetic fiber and process for preparation thereof |
| US3991236A (en) * | 1968-11-22 | 1976-11-09 | Vepa Ag | Method for coating a material length with a fluid coating substance |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB499207A (en) * | 1935-09-12 | 1939-01-16 | Tootal Broadhurst Lee Co Ltd | Improved process for delustring and rendering textile fabrics crease-resisting |
| US2190672A (en) * | 1936-03-14 | 1940-02-20 | Bakelite Corp | Water-soluble phenol-aldehyde resins |
| US2709141A (en) * | 1952-06-28 | 1955-05-24 | Kendall & Co | Resin-treated regenerated cellulose textile material and method of making the same |
| US2804441A (en) * | 1954-04-22 | 1957-08-27 | Monsanto Chemicals | Compositions of methyl ethers of polymethylol melamine and a catalyst |
| US2844488A (en) * | 1955-02-02 | 1958-07-22 | Goodyear Tire & Rubber | Process for treating nylon cord fabric |
| US2852479A (en) * | 1953-08-28 | 1958-09-16 | American Cyanamid Co | Process of preparing an aqueous dispersion of melamine formaldehyde, pigment, and non-ionic surface active agent, product obtained and process of using |
-
1956
- 1956-11-01 GB GB3336256A patent/GB865857A/en not_active Expired
-
1957
- 1957-10-17 US US69061557 patent/US2974065A/en not_active Expired - Lifetime
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB499207A (en) * | 1935-09-12 | 1939-01-16 | Tootal Broadhurst Lee Co Ltd | Improved process for delustring and rendering textile fabrics crease-resisting |
| US2190672A (en) * | 1936-03-14 | 1940-02-20 | Bakelite Corp | Water-soluble phenol-aldehyde resins |
| US2709141A (en) * | 1952-06-28 | 1955-05-24 | Kendall & Co | Resin-treated regenerated cellulose textile material and method of making the same |
| US2852479A (en) * | 1953-08-28 | 1958-09-16 | American Cyanamid Co | Process of preparing an aqueous dispersion of melamine formaldehyde, pigment, and non-ionic surface active agent, product obtained and process of using |
| US2804441A (en) * | 1954-04-22 | 1957-08-27 | Monsanto Chemicals | Compositions of methyl ethers of polymethylol melamine and a catalyst |
| US2844488A (en) * | 1955-02-02 | 1958-07-22 | Goodyear Tire & Rubber | Process for treating nylon cord fabric |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3242119A (en) * | 1960-03-22 | 1966-03-22 | Ciba Ltd | Water soluble synthetic resin compositions comprising a melamine-formaldehyde condensate and an unoxidized alkyd resin |
| US3218119A (en) * | 1962-02-02 | 1965-11-16 | American Cyanamid Co | Method of applying cyclic urea resins to cellulosic textile materials |
| US3177093A (en) * | 1962-06-06 | 1965-04-06 | American Cyanamid Co | Method of treating cellulose textile material and the treated material |
| US3890095A (en) * | 1967-04-05 | 1975-06-17 | American Cyanamid Co | Cellulosic textile finish with 1,3-dimethylol-4,5-dihydroxy-2-imidazolidinone, zinc nitrate and a sequestering agent |
| US3991236A (en) * | 1968-11-22 | 1976-11-09 | Vepa Ag | Method for coating a material length with a fluid coating substance |
| US3950589A (en) * | 1972-03-23 | 1976-04-13 | Toray Industries, Inc. | Melt-resistant synthetic fiber and process for preparation thereof |
| US3916063A (en) * | 1973-10-11 | 1975-10-28 | Thilmany Pulp & Paper Company | Method for manufacturing a printable, glueable polyolefin web material |
Also Published As
| Publication number | Publication date |
|---|---|
| GB865857A (en) | 1961-04-19 |
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