US3291560A - Method of forming polymers on fibrous substrates through high velocity impingement with solutions containing unsaturated monomers and chemical catalysts - Google Patents
Method of forming polymers on fibrous substrates through high velocity impingement with solutions containing unsaturated monomers and chemical catalysts Download PDFInfo
- Publication number
- US3291560A US3291560A US243671A US24367162A US3291560A US 3291560 A US3291560 A US 3291560A US 243671 A US243671 A US 243671A US 24367162 A US24367162 A US 24367162A US 3291560 A US3291560 A US 3291560A
- Authority
- US
- United States
- Prior art keywords
- fibers
- vinyl
- wool
- peroxide
- monomer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 51
- 239000003054 catalyst Substances 0.000 title claims description 31
- 239000000758 substrate Substances 0.000 title claims description 13
- 239000000126 substance Substances 0.000 title claims description 6
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- 229920000642 polymer Polymers 0.000 title description 11
- 239000000835 fiber Substances 0.000 claims description 97
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- SNVLJLYUUXKWOJ-UHFFFAOYSA-N methylidenecarbene Chemical compound C=[C] SNVLJLYUUXKWOJ-UHFFFAOYSA-N 0.000 claims 1
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- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- TUORNJBNFQTQDL-UHFFFAOYSA-N methyl 2-[(2-methoxy-2-oxoethyl)-(2-methylprop-2-enoyl)amino]acetate Chemical compound C(C(=C)C)(=O)N(CC(=O)OC)CC(=O)OC TUORNJBNFQTQDL-UHFFFAOYSA-N 0.000 description 1
- AWJZTPWDQYFQPQ-UHFFFAOYSA-N methyl 2-chloroprop-2-enoate Chemical compound COC(=O)C(Cl)=C AWJZTPWDQYFQPQ-UHFFFAOYSA-N 0.000 description 1
- HKVOGMDMMCLQFJ-UHFFFAOYSA-N methyl 3-thiophen-2-ylprop-2-enoate Chemical compound COC(=O)C=CC1=CC=CS1 HKVOGMDMMCLQFJ-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- AMBKPYJJYUKNFI-UHFFFAOYSA-N methylsulfanylethene Chemical compound CSC=C AMBKPYJJYUKNFI-UHFFFAOYSA-N 0.000 description 1
- WFKDPJRCBCBQNT-UHFFFAOYSA-N n,2-dimethylprop-2-enamide Chemical compound CNC(=O)C(C)=C WFKDPJRCBCBQNT-UHFFFAOYSA-N 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical group CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- KNFILXSWEXSJCV-UHFFFAOYSA-N n-ethenyl-n,4-dimethylbenzenesulfonamide Chemical compound C=CN(C)S(=O)(=O)C1=CC=C(C)C=C1 KNFILXSWEXSJCV-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- XNTUJOTWIMFEQS-UHFFFAOYSA-N octadecanoyl octadecaneperoxoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCCCCCCCC XNTUJOTWIMFEQS-UHFFFAOYSA-N 0.000 description 1
- SRSFOMHQIATOFV-UHFFFAOYSA-N octanoyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(=O)CCCCCCC SRSFOMHQIATOFV-UHFFFAOYSA-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
- 239000012934 organic peroxide initiator Substances 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- DJEHXEMURTVAOE-UHFFFAOYSA-M potassium bisulfite Chemical compound [K+].OS([O-])=O DJEHXEMURTVAOE-UHFFFAOYSA-M 0.000 description 1
- 229940099427 potassium bisulfite Drugs 0.000 description 1
- 235000010259 potassium hydrogen sulphite Nutrition 0.000 description 1
- ZOCLAPYLSUCOGI-UHFFFAOYSA-M potassium hydrosulfide Chemical compound [SH-].[K+] ZOCLAPYLSUCOGI-UHFFFAOYSA-M 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- QROGIFZRVHSFLM-UHFFFAOYSA-N prop-1-enylbenzene Chemical class CC=CC1=CC=CC=C1 QROGIFZRVHSFLM-UHFFFAOYSA-N 0.000 description 1
- FJVVXDAWKSUUHP-UHFFFAOYSA-N propanoyl benzenecarboperoxoate Chemical compound CCC(=O)OOC(=O)C1=CC=CC=C1 FJVVXDAWKSUUHP-UHFFFAOYSA-N 0.000 description 1
- KOPQZJAYZFAPBC-UHFFFAOYSA-N propanoyl propaneperoxoate Chemical compound CCC(=O)OOC(=O)CC KOPQZJAYZFAPBC-UHFFFAOYSA-N 0.000 description 1
- 239000012857 radioactive material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 1
- MNCGMVDMOKPCSQ-UHFFFAOYSA-M sodium;2-phenylethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=CC1=CC=CC=C1 MNCGMVDMOKPCSQ-UHFFFAOYSA-M 0.000 description 1
- BWYYYTVSBPRQCN-UHFFFAOYSA-M sodium;ethenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C=C BWYYYTVSBPRQCN-UHFFFAOYSA-M 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 125000004079 stearyl 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])([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])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- PQEXLIRUMIRSAL-UHFFFAOYSA-N tert-butyl 4-(2-ethoxy-2-oxoethyl)piperidine-1-carboxylate Chemical compound CCOC(=O)CC1CCN(C(=O)OC(C)(C)C)CC1 PQEXLIRUMIRSAL-UHFFFAOYSA-N 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- VKFFEYLSKIYTSJ-UHFFFAOYSA-N tetraazanium;phosphonato phosphate Chemical compound [NH4+].[NH4+].[NH4+].[NH4+].[O-]P([O-])(=O)OP([O-])([O-])=O VKFFEYLSKIYTSJ-UHFFFAOYSA-N 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- UMFJXASDGBJDEB-UHFFFAOYSA-N triethoxy(prop-2-enyl)silane Chemical compound CCO[Si](CC=C)(OCC)OCC UMFJXASDGBJDEB-UHFFFAOYSA-N 0.000 description 1
- IDDWGDKSBYYEPL-VQHVLOKHSA-N triethyl (e)-prop-1-ene-1,2,3-tricarboxylate Chemical compound CCOC(=O)C\C(C(=O)OCC)=C/C(=O)OCC IDDWGDKSBYYEPL-VQHVLOKHSA-N 0.000 description 1
- DZAIBGWGBBQGPZ-XQRVVYSFSA-N trimethyl (z)-prop-1-ene-1,2,3-tricarboxylate Chemical compound COC(=O)C\C(C(=O)OC)=C\C(=O)OC DZAIBGWGBBQGPZ-XQRVVYSFSA-N 0.000 description 1
- VJUIXFPWWBZVIL-UHFFFAOYSA-N trimethyl-[prop-2-enyl(trimethylsilyloxy)silyl]oxysilane Chemical compound C[Si](C)(C)O[SiH](CC=C)O[Si](C)(C)C VJUIXFPWWBZVIL-UHFFFAOYSA-N 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- YCJYNBLLJHFIIW-MBABXGOBSA-N validoxylamine A Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)C[C@@H]1N[C@@H]1[C@H](O)[C@@H](O)[C@H](O)C(CO)=C1 YCJYNBLLJHFIIW-MBABXGOBSA-N 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
- 238000009976 warp beam dyeing Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- CAAIULQYGCAMCD-UHFFFAOYSA-L zinc;hydroxymethanesulfinate Chemical compound [Zn+2].OCS([O-])=O.OCS([O-])=O CAAIULQYGCAMCD-UHFFFAOYSA-L 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01H—ELECTRIC SWITCHES; RELAYS; SELECTORS; EMERGENCY PROTECTIVE DEVICES
- H01H85/00—Protective devices in which the current flows through a part of fusible material and this current is interrupted by displacement of the fusible material when this current becomes excessive
- H01H85/02—Details
- H01H85/26—Magazine arrangements
- H01H85/28—Magazine arrangements effecting automatic replacement
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B5/00—Forcing liquids, gases or vapours through textile materials to effect treatment, e.g. washing, dyeing, bleaching, sizing impregnating
-
- 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
- D06M14/00—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
-
- 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
- D06M14/00—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
- D06M14/02—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials on to materials of natural origin
- D06M14/06—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials on to materials of natural origin of animal origin, e.g. wool or silk
-
- 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
- D06M14/00—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
- D06M14/18—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation
-
- 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
- D06M14/00—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
- D06M14/18—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation
- D06M14/20—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation on to materials of natural origin
- D06M14/24—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials using wave energy or particle radiation on to materials of natural origin of animal origin, e.g. wool or silk
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06B—TREATING TEXTILE MATERIALS USING LIQUIDS, GASES OR VAPOURS
- D06B2700/00—Treating of textile materials, e.g. bleaching, dyeing, mercerising, impregnating, washing; Fulling of fabrics
- D06B2700/18—Passing liquid through fibrous materials in closed containers with a form not determined by the nature of the fibrous material
Definitions
- Yet another object of this invention is to provide such a process wherein said compounds are applied uniformly to the keratin fibers being treated.
- Wool fibers are generally treated with an aqueous solution of the desired monomer or low polymer in the presence of a catalyst system capable of inducing polymerization thereof.
- the catalyst system most generally used is a redox catalyst system composed of a reducing agent and an oxidizing agent.
- the prior art teaches that wool fibers should be impregnated with one of these catalyst components and then contacted with the monomer and the other catalyst component, in the belief that the monomer will polymerize in a solution containing both catalyst components. This in fact does occur in many of the prior art immersion baths. For some reason, again unexplainable, the expected polymerization does not occur when a single system containing the desired monomer and all catalyst components is applied to wool fibers under the conditions of flow utilized in accordance with this invention. This characteristic of the invention, therefore, constitutes a distinct advantage of this invention over the prior art immersion techniques in that far superior control of the process is possible when all components can be added from a single bath.
- the preferred redox catalyst system is composed of a reducing agent and an oxidizing agent initiator, the interaction of which provides free radicals which cause polymerization of the monomeric or low polymeric material with the keratin substrate.
- organic peroxide initiators that can be employed are the following: tetralin hydroperoxide, tert.-butyl diperphthalate, cumene hydroperoxide, tert.- butyl perbenzoate, 2,4-dichlorobenzoyl peroxide, urea peroxide, caprylyl peroxide, p-chlorobenzoyl peroxide, 2,2-bis(tert.-butyl peroxy) butane, hydroxyheptyl peroxide, diperoxide of benzaldehyde.
- each wool sample treated is scoured by immersing in or having passed therethrough in the package dye machine, an aqueous solution containing 0.5% on the weight of wool of surfonic N-95, anon-ionic surface active agent and 1.5% onthe weight of wool of glacial acetic acid. After scouring for 20 minutes at 140 F. the sample is rinsed in water at F. for 10-15 minutes. Deionized water is used in preparing all aqueous media.
- fabrics of improved handle can be provided by treating fibers in generally lose form and processing them into fabrics.
- This process can be greatly improved by conducting the process under certain conditions of forced flow.
- the small amounts, or absence, of homopolymer when these processes are conducted under certain conditions of flow eliminates the necessity for conducting extraction techniques,
- a process for modifying the characteristics of continuous lengths of loose, non-woven textile fibers which are confined in a given configuration throughout the modification comprising providing a solution of a compound containing the group and a fibrous substrate; forcing said solution at a rate substantially greater than that possible as a result of merely refluxing said fibers in said solution through said fibrous substrate unidirectionally, intermittently back and forth throughout the process, said process being conducted in the presence of a chemical catalyst for the polymerization of said compound.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL301459D NL301459A (enrdf_load_stackoverflow) | 1962-12-10 | ||
US243671A US3291560A (en) | 1962-12-10 | 1962-12-10 | Method of forming polymers on fibrous substrates through high velocity impingement with solutions containing unsaturated monomers and chemical catalysts |
FR955804A FR1387915A (fr) | 1962-12-10 | 1963-12-03 | Nouveau procédé pour modifier les caractéristiques des fibres de kératine |
GB47714/63A GB1067494A (en) | 1962-12-10 | 1963-12-03 | Treatment of textile fibres |
CH1484363A CH461425A (fr) | 1962-12-10 | 1963-12-04 | Procédé pour perfectionner des fibres textiles par greffage d'un composé vinylique |
DE19631444052 DE1444052A1 (de) | 1962-12-10 | 1963-12-06 | Verfahren zum Modifizieren von Textilfasern |
BE640927A BE640927A (enrdf_load_stackoverflow) | 1962-12-10 | 1963-12-06 | |
LU44983D LU44983A1 (enrdf_load_stackoverflow) | 1962-12-10 | 1963-12-10 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US243671A US3291560A (en) | 1962-12-10 | 1962-12-10 | Method of forming polymers on fibrous substrates through high velocity impingement with solutions containing unsaturated monomers and chemical catalysts |
Publications (1)
Publication Number | Publication Date |
---|---|
US3291560A true US3291560A (en) | 1966-12-13 |
Family
ID=22919647
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US243671A Expired - Lifetime US3291560A (en) | 1962-12-10 | 1962-12-10 | Method of forming polymers on fibrous substrates through high velocity impingement with solutions containing unsaturated monomers and chemical catalysts |
Country Status (7)
Country | Link |
---|---|
US (1) | US3291560A (enrdf_load_stackoverflow) |
BE (1) | BE640927A (enrdf_load_stackoverflow) |
CH (1) | CH461425A (enrdf_load_stackoverflow) |
DE (1) | DE1444052A1 (enrdf_load_stackoverflow) |
GB (1) | GB1067494A (enrdf_load_stackoverflow) |
LU (1) | LU44983A1 (enrdf_load_stackoverflow) |
NL (1) | NL301459A (enrdf_load_stackoverflow) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3457028A (en) * | 1962-12-06 | 1969-07-22 | Deering Milliken Res Corp | Modifying keratinic fibers with solutions containing unsaturated monomers and redox catalysts while maintaining a shear force on said solutions |
US3475114A (en) * | 1962-12-06 | 1969-10-28 | Deering Milliken Res Corp | Modification of keratin fibers with ethylenically unsaturated compounds in the presence of aqueous solutions of fiber swelling agents |
US3633591A (en) * | 1969-05-29 | 1972-01-11 | Colgate Palmolive Co | Treatment of keratinous substrates with a reducing agent and thereafter an oxidizing solution of a vinyl monomer |
US3634022A (en) * | 1969-05-29 | 1972-01-11 | Colgate Palmolive Co | Form-setting keratin substrates by a chemical treatment involving a vinyl monomer |
US3909195A (en) * | 1962-12-06 | 1975-09-30 | Deering Milliken Res Corp | Process of modifying textile materials with polymerizable monomers |
US4743267A (en) * | 1982-06-21 | 1988-05-10 | International Yarn Corporation Of Tennessee | Process for improving polymer fiber properties and fibers produced thereby |
US20080066773A1 (en) * | 2006-04-21 | 2008-03-20 | Anderson Daniel G | In situ polymerization for hair treatment |
US11912959B2 (en) | 2019-04-30 | 2024-02-27 | Schreiber Gmbh | Boron-free impregnating solution for a wick and boron-free wick |
-
0
- NL NL301459D patent/NL301459A/xx unknown
-
1962
- 1962-12-10 US US243671A patent/US3291560A/en not_active Expired - Lifetime
-
1963
- 1963-12-03 GB GB47714/63A patent/GB1067494A/en not_active Expired
- 1963-12-04 CH CH1484363A patent/CH461425A/fr unknown
- 1963-12-06 BE BE640927A patent/BE640927A/xx unknown
- 1963-12-06 DE DE19631444052 patent/DE1444052A1/de active Pending
- 1963-12-10 LU LU44983D patent/LU44983A1/xx unknown
Non-Patent Citations (1)
Title |
---|
None * |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3457028A (en) * | 1962-12-06 | 1969-07-22 | Deering Milliken Res Corp | Modifying keratinic fibers with solutions containing unsaturated monomers and redox catalysts while maintaining a shear force on said solutions |
US3475114A (en) * | 1962-12-06 | 1969-10-28 | Deering Milliken Res Corp | Modification of keratin fibers with ethylenically unsaturated compounds in the presence of aqueous solutions of fiber swelling agents |
US3909195A (en) * | 1962-12-06 | 1975-09-30 | Deering Milliken Res Corp | Process of modifying textile materials with polymerizable monomers |
US3633591A (en) * | 1969-05-29 | 1972-01-11 | Colgate Palmolive Co | Treatment of keratinous substrates with a reducing agent and thereafter an oxidizing solution of a vinyl monomer |
US3634022A (en) * | 1969-05-29 | 1972-01-11 | Colgate Palmolive Co | Form-setting keratin substrates by a chemical treatment involving a vinyl monomer |
US3676550A (en) * | 1969-05-29 | 1972-07-11 | Colgate Palmolive Co | Modification of reduced keratinous substrates with a vinyl monomer |
US4743267A (en) * | 1982-06-21 | 1988-05-10 | International Yarn Corporation Of Tennessee | Process for improving polymer fiber properties and fibers produced thereby |
US20080066773A1 (en) * | 2006-04-21 | 2008-03-20 | Anderson Daniel G | In situ polymerization for hair treatment |
US11912959B2 (en) | 2019-04-30 | 2024-02-27 | Schreiber Gmbh | Boron-free impregnating solution for a wick and boron-free wick |
EP3963027B1 (de) * | 2019-04-30 | 2024-08-28 | Schreiber GmbH | Borfreier docht und verfahren zu dessen herstellung |
Also Published As
Publication number | Publication date |
---|---|
CH461425A (fr) | 1968-10-31 |
DE1444052A1 (de) | 1969-07-24 |
LU44983A1 (enrdf_load_stackoverflow) | 1964-02-11 |
NL301459A (enrdf_load_stackoverflow) | |
GB1067494A (en) | 1967-05-03 |
BE640927A (enrdf_load_stackoverflow) | 1964-04-01 |
CH1484363A4 (enrdf_load_stackoverflow) | 1968-05-15 |
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