US2061565A - Treatment of fibers or like materials - Google Patents
Treatment of fibers or like materials Download PDFInfo
- Publication number
- US2061565A US2061565A US668069A US66806933A US2061565A US 2061565 A US2061565 A US 2061565A US 668069 A US668069 A US 668069A US 66806933 A US66806933 A US 66806933A US 2061565 A US2061565 A US 2061565A
- Authority
- US
- United States
- Prior art keywords
- materials
- stretching
- cellulose
- soaps
- softening
- 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 description 28
- 238000011282 treatment Methods 0.000 title description 10
- 239000000835 fiber Substances 0.000 title description 3
- 229920002678 cellulose Polymers 0.000 description 21
- 239000000344 soap Substances 0.000 description 20
- 229920002301 cellulose acetate Polymers 0.000 description 18
- 239000003921 oil Substances 0.000 description 17
- 235000019198 oils Nutrition 0.000 description 17
- 235000010980 cellulose Nutrition 0.000 description 13
- 239000003795 chemical substances by application Substances 0.000 description 13
- 239000003925 fat Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 13
- 230000008961 swelling Effects 0.000 description 13
- 239000001913 cellulose Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000012736 aqueous medium Substances 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 150000002170 ethers Chemical class 0.000 description 6
- 239000002609 medium Substances 0.000 description 6
- 238000007127 saponification reaction Methods 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229920003086 cellulose ether Polymers 0.000 description 5
- 238000004804 winding Methods 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 229940116333 ethyl lactate Drugs 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000004902 Softening Agent Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000000944 linseed oil Substances 0.000 description 3
- 235000021388 linseed oil Nutrition 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 235000014676 Phragmites communis Nutrition 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- -1 aromatic series naphthalene sulphonic acid compounds Chemical class 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 230000001112 coagulating effect Effects 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 238000000578 dry spinning Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 235000011121 sodium hydroxide Nutrition 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000002166 wet spinning Methods 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- UTACNSITJSJFHA-UHFFFAOYSA-N 1,1,1,3-tetrachloropropane Chemical compound ClCCC(Cl)(Cl)Cl UTACNSITJSJFHA-UHFFFAOYSA-N 0.000 description 1
- KFUSEUYYWQURPO-UHFFFAOYSA-N 1,2-dichloroethene Chemical group ClC=CCl KFUSEUYYWQURPO-UHFFFAOYSA-N 0.000 description 1
- YRJSLCBKZMMEPB-UHFFFAOYSA-N 2-(2-methylpropyl)naphthalene-1-sulfonic acid Chemical class C1=CC=CC2=C(S(O)(=O)=O)C(CC(C)C)=CC=C21 YRJSLCBKZMMEPB-UHFFFAOYSA-N 0.000 description 1
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 1
- ZTFYJIXFKGPCHV-UHFFFAOYSA-N 2-propan-2-ylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(C(C)C)=CC=C21 ZTFYJIXFKGPCHV-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 235000003911 Arachis Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 108700040458 Drosophila Strn-Mlck Proteins 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- KNNPTLFTAWALOI-UHFFFAOYSA-N acetaldehyde;formaldehyde Chemical compound O=C.CC=O KNNPTLFTAWALOI-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- JCZMXVGQBBATMY-UHFFFAOYSA-N nitro acetate Chemical compound CC(=O)O[N+]([O-])=O JCZMXVGQBBATMY-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010499 rapseed oil Substances 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000010698 whale oil Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F2/00—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof
- D01F2/24—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives
- D01F2/28—Monocomponent artificial filaments or the like of cellulose or cellulose derivatives; Manufacture thereof from cellulose derivatives from organic cellulose esters or ethers, e.g. cellulose acetate
Definitions
- This invention relates to improvements in the treatment of fibers or like materials and is particularly concerned with the manufacture of filamentsthreads, yarns, ribbons and the like of cellulose acetate or other cellulose esters or ethers.
- the permanent stretch may be as much as 100% or more of the original length of the filaments or other materials.
- the stretching is assisted by treating the materials either before or during the stretching operation with solvents or softening agents for the cellulose acetate or other cellulose derivative.
- animal or vegetable oil including sulphonated soaps, may be used for the purpose of the present invention.
- castor oil olive oil, cocoanut oil, arachis oil, cotton seed oil, rape oil and whale oil, raw or hardened.
- soaps obtainable from such oils, for example sodium,
- ammonium or potassium oleate or ethanolamine oleates or other-organic soaps of oleic acid the soaps obtainable from the cocoanut oil fat acids, and the soaps of lauric, palmitic, 'stearic or' ricinoleic acids or sulphonated soaps obtainable from any of these compounds.
- Other fatty bodies such as sulphonated fatty alcohols and the w-alkylamides of fatty acids and their sulphonated derivatives, may be used for the purposes of the present invention, while examples of aromatic compounds are the alkylated naphthalene sulphonic acids, e. g. isopropyl naphthalene sulphonic acid.
- Most of the above substances are wetting agents, and it is found that the use of this 'classof substance broadly is of value for the purpose of the present invention.
- oils will be soluble in the medium .used to assist the stretching treatment. If insoluble they may be emulsified therewith, for example by means of soaps, sulphonated fats or oils or salts thereof, such as sulphonated castor oil, true sulphonic acids of aliphatic hydrocarbons or alcohols orof fatty acids or salts thereof, ethanolamine and other alkylolamine soaps and amino-alkylamides of higher fatty acids and in the aromatic series naphthalene sulphonic acid compounds and particularly alkylated naphtha-' lene sulphonic acids, such as propyl and iso-butyl naphthalene sulphonic acids and the sulphonated condensation products of formaldehyde and naphthalene.
- soaps sulphonated fats or oils or salts thereof, such as sulphonated castor oil, true sulphonic acids of aliphatic hydrocarbons or alcohols orof fatty acids or salts
- Such emulsifying agents are particularly useful where the swelling medium is aqueous in character.
- the swelling medium consists of a solvent or strong swelling agent for the cellulose derivative and a nonaqueous diluent the oil or fat will be soluble therein in practically all cases.
- suitable solvents or swelling agents for assisting the stretching of the cellulose acetatev or other cellulose ester or ether are suitable emulsifying agents lowing may be instanced:aqueous solutions of thiocyanates, such as those of the alkalies, ammonium and alkaline earths, aqueous solutions of zinc chloride, acetic acid, formic acid, lactic acid, diacetone alcohol, acetone and the like; the ethers, esters or ether-esters of olefine glycols and polyolefine glycols or of other polyhydric alcohols for instance the monoand di-methyl and ethyl ethers of ethylene glycol, the mono-methyl and ethyl ethers of propylene glycol, and the monoethyl ether of diethylene glycol, dioxane, methylene ethylene dioxide and their homologues and substitution products, e.
- thiocyanates such as those of the alkalies, ammonium and alkaline earths,
- dioxane dicarbinyl diacetate glycol mono-acetate, methyl glycol monoacetate, mono-, di-, and tri-acetins, ethyl lactate etc.; phenols, formaldehyde acetaldehyde, dichlorethylene methylene chloride and the like, or mixtures of these, or solvent mixtures.
- solvents or swelling agents may if necessary be diluted with water, though the methylene chloride or dichlorethylene type of solvent is immiscible with water, so that dilution should be effected with a non-aqueous diluent miscible therewith, as for example benezene, carbon tetrachloride, perchlorethylene and the like.
- the stretching operation may in the present invention be conducted on the travelling filaments, yarns, etc., as described in U. S. application S. No. 378,684, the operation being conducted for example in a bobbin to bobbin operation, or in a cheese winding operation or in any other rewlnding operation or in the course of the travel of the filaments from a wet or dry spinning machine to a winding device.
- U. S. application S. No. 662,844 filed 2nd April, 1932 considerable advantages accrue by carrying out the stretching operation while the yarns, threads or the like are in warp formation, that is to say a large number of threads are aligned side by side and are stretched by a single stretchin'g device.
- the stretch may be inserted in one single stretching operation or it may be inserted in stages, in which case it is of advantage as de scribed in U. S. application S. No. 573,424 filed 6th November, 1931, to maintain the filaments or the like in a softened or plastic state between the stretching stages.
- the materials Prior to the softening treatment which immediately precedes the stretching or which is effected simultaneously therewith, the materials may be subjected to a pretreatment with softening agents of strengths diiferent from thatused in the final softening treatment, as is described in U. S. application S. No. 638,776 filed 20th October, 1932.
- the process of the present invention may be employed in connection with any one or more of such softening treatments.
- ethers of all kinds for instance cellulose formate
- esters or ethers may be of lowfmedium or high viscosity characteristics; for instance cellulose acetates having a viscosity of 5-10, 20-30 or-50-100 or 200 or more as measured by comparing the viscosity of a 6% solution in acetone against a standard of glycerine taken as may be present in the materials.
- yarns or other materials may consist wholly of the cellulose ester or ether or may contain other materials not deleteriously affected by the treatment.
- cellulose ester materials may be subjected to a. saponification which may be superficial, may be partial and uniform or may be complete. Such saponification may take place immediately after the stretching treatment of the present invention, or, particularly where the cellulose esters are subjected to a partial and substantially uniform saponification, may immediately precede the stretching treatment.
- the saponification may be effected with the aid of aqueous or aqueous alcoholic or alcoholic caustic soda, caustic potash, trisodium phosphate or other alkaline salt or reagent or may be effected with ammonia or organic amine in the vapour state.
- the saponifying media may contain sodium acetate or soaps or other buffer substances and may contain in addition to or in place of methyl alcohol or ethyl alcohol lime or other substances whereby the amount of caustic soda necessary for effecting any desired degree of saponification may be less than that theoretically
- the saponifying media may themselves contain oils or fats as with the stretching media of the present invention.
- Example 1 A cellulose acetate yarn in hank form is softened in a bath consisting of an emulsion of linseed oil in aqueous ethyl lactate prepared e. g. in the following manner. 8 parts of oleic acid, 2 parts of tri-ethanolamine and 30 parts of linseed oil are thoroughly mixed at ordinary temperatures and 30 parts of 50% aqueous ethyl lactate are then slowly added to the mixture with constant. and vigorous stirring until an emulsion is obtained. A further 60 parts of linseed oil are then added in small proportions with continual stirring. The emulsion is then diluted to 10 times its volume with 50% ethyl lactate which is added in small proportions at the beginning with constant stirring and then in larger amounts until the whole has been introduced and a satisfactory emulsion is obtained.
- aqueous ethyl lactate prepared e. g. in the following manner. 8 parts of oleic acid, 2 parts of tri-ethanolamine and 30
- the hanks are soaked in the emulsion for about 5-l0 minutes at 20-25 C. and then stretched, for example by 100 to 200% of their original length and are found to have an increased tenacity.
- Example 2 A number of cellulose acetate threads are taken from a creel of bobbins and led over a roller in warp formation into a stretching bath consisting of a 45-50% solution of dioxane containing 1 to 2% of the sodium salt of the sulphuric ester of lauryl alcohol. From the feed roller the warp passes through a reed to keep the threads apart, under a guide and then down the bath which is 80 to 100 feet long, through a; reed at the further end, round a draw-roller and then to washing, drying and winding devices.
- the peripheral speed of the feed roller is about 5 to 7 metres per minute while that of the draw-roller is 20 to 30 metres per minute so that a stretch of 400 to 500% is obtained.
- the temperature-of the bath is 20 to 25 C.
- the threads which have been stretched according to the example are found to have considerably greater tenacity than before stretching.
- Example 3 A 25% solution of cellulose acetate in acetone 'is extruded into a coagulating bath consisting of example 1 to 1.5. After passing over a drawroller the filaments are washed to remove excess solvent, preferably with solutions of solvent in lower concentration or with salt solutions and are then dried and wound. Materials having an improved tenacity are thus obtained.
- swelling agent as employed hereinafter in the claims is to be understood as including not only agents which exert only a swelling action on the cellulose derivative, but also agents which are true solvents therefor.
- Process for the manufacture of high tenacity filaments, threads, yarns, ribbons and like materials containing cellulose acetate which comprises forming the materials by extruding a suitable solution of cellulose acetate into an aqueous medium throughout which are uniformly distributed a swelling agent for cellulose acetate'and a substance selected from the group consisting of oils, fats and soaps; and stretching the materials during their formation.
- Process for the manufacture of high tenacity filaments, threads, yarns, ribbons and like materials containing cellulose acetate which comprises forming the materials by extruding a suitable solution of cellulose acetate into an aqueous medium in which are dissolved a swelling agent for cellulose acetate and a substance selected from the group consisting of oils, fats and soaps, and stretching the materials during their formation.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Textile Engineering (AREA)
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Description
Patented Nov. 24, 1936 UNITED STATES TREATDIENT OF FIBERS OR LIKE MATERIALS Henry Dreyfus, London, England I No Drawing. Application April 26, 1933, Serial 8 Claims.
This invention relates to improvements in the treatment of fibers or like materials and is particularly concerned with the manufacture of filamentsthreads, yarns, ribbons and the like of cellulose acetate or other cellulose esters or ethers. y
In U. S. Patent No. 1,709,470 processes are described for the treatment of cellulose acetate filaments, threads or the like in which such products are subjected to a stretching operation at any stage of theirmanufacture after they have reached the'fully set and finished condition, such stretch being beyond the elastic limit, theproducts thereby acquiring an increased resistance to the action of hot or boiling aqueous media, and also being reduced in' denier.
for example from bobbin to bobbin -or from any other package to a winding device or from a dry spinning machine to a- Winding device. The
permanent stretch may be as much as 100% or more of the original length of the filaments or other materials. The stretching is assisted by treating the materials either before or during the stretching operation with solvents or softening agents for the cellulose acetate or other cellulose derivative.
Again, U.' S. applications S. Nos. 402,785 filed 20th October, 1929, 418,414 filed 3rd January, 1930, 437,423 filed 20th March, 1930, 589,428filed 28th 'January, 1932, 681,043 filed 24th March, 1932 and 607,668 filed 26th April, 1932 describe processes in which solutions of cellulose acetate or .other cellulose esters 'or ethers are spun by wet spinning methods into coagulating media eluding with the solvent or other softening agent an oily or a fatty body or a soap. The oil, fat
- fied 1n the medium. Any suitable animal or vegetable oil or a soap which may be made from an Such a, stretching results in an increased, tensile strength. U. S.
In Great Britain May 6, 1932 animal or vegetable oil, including sulphonated soaps, may be used for the purpose of the present invention. Thus, for instance, there may be used castor oil, olive oil, cocoanut oil, arachis oil, cotton seed oil, rape oil and whale oil, raw or hardened. Again, there may be employed the soaps obtainable from such oils, for example sodium,
ammonium or potassium oleate or ethanolamine oleates or other-organic soaps of oleic acid, the soaps obtainable from the cocoanut oil fat acids, and the soaps of lauric, palmitic, 'stearic or' ricinoleic acids or sulphonated soaps obtainable from any of these compounds. Other fatty bodies, such as sulphonated fatty alcohols and the w-alkylamides of fatty acids and their sulphonated derivatives, may be used for the purposes of the present invention, while examples of aromatic compounds are the alkylated naphthalene sulphonic acids, e. g. isopropyl naphthalene sulphonic acid. Most of the above substances are wetting agents, and it is found that the use of this 'classof substance broadly is of value for the purpose of the present invention.
In general proportions of 1-5 up to 10% of oil or the like on the total softening medium are suitable, though the invention is nothmited thereto, and lower or higher proportions may of course be employed.
In most cases the oils will be soluble in the medium .used to assist the stretching treatment. If insoluble they may be emulsified therewith, for example by means of soaps, sulphonated fats or oils or salts thereof, such as sulphonated castor oil, true sulphonic acids of aliphatic hydrocarbons or alcohols orof fatty acids or salts thereof, ethanolamine and other alkylolamine soaps and amino-alkylamides of higher fatty acids and in the aromatic series naphthalene sulphonic acid compounds and particularly alkylated naphtha-' lene sulphonic acids, such as propyl and iso-butyl naphthalene sulphonic acids and the sulphonated condensation products of formaldehyde and naphthalene. Such emulsifying agents are particularly useful where the swelling medium is aqueous in character. Where the swelling medium consists of a solvent or strong swelling agent for the cellulose derivative and a nonaqueous diluent the oil or fat will be soluble therein in practically all cases.
where the continuous phase of the emulsion required is non-aqueous.
As examples of suitable solvents or swelling agents for assisting the stretching of the cellulose acetatev or other cellulose ester or ether the fol- Magnesium or even calcium soaps are suitable emulsifying agents lowing may be instanced:aqueous solutions of thiocyanates, such as those of the alkalies, ammonium and alkaline earths, aqueous solutions of zinc chloride, acetic acid, formic acid, lactic acid, diacetone alcohol, acetone and the like; the ethers, esters or ether-esters of olefine glycols and polyolefine glycols or of other polyhydric alcohols for instance the monoand di-methyl and ethyl ethers of ethylene glycol, the mono-methyl and ethyl ethers of propylene glycol, and the monoethyl ether of diethylene glycol, dioxane, methylene ethylene dioxide and their homologues and substitution products, e. g. dioxane dicarbinyl diacetate, glycol mono-acetate, methyl glycol monoacetate, mono-, di-, and tri-acetins, ethyl lactate etc.; phenols, formaldehyde acetaldehyde, dichlorethylene methylene chloride and the like, or mixtures of these, or solvent mixtures. In most cases such solvents or swelling agents may if necessary be diluted with water, though the methylene chloride or dichlorethylene type of solvent is immiscible with water, so that dilution should be effected with a non-aqueous diluent miscible therewith, as for example benezene, carbon tetrachloride, perchlorethylene and the like.
The stretching operation may in the present invention be conducted on the travelling filaments, yarns, etc., as described in U. S. application S. No. 378,684, the operation being conducted for example in a bobbin to bobbin operation, or in a cheese winding operation or in any other rewlnding operation or in the course of the travel of the filaments from a wet or dry spinning machine to a winding device. As is indicated in U. S. application S. No. 662,844 filed 2nd April, 1932, considerable advantages accrue by carrying out the stretching operation while the yarns, threads or the like are in warp formation, that is to say a large number of threads are aligned side by side and are stretched by a single stretchin'g device. The stretch may be inserted in one single stretching operation or it may be inserted in stages, in which case it is of advantage as de scribed in U. S. application S. No. 573,424 filed 6th November, 1931, to maintain the filaments or the like in a softened or plastic state between the stretching stages.
Prior to the softening treatment which immediately precedes the stretching or which is effected simultaneously therewith, the materials may be subjected to a pretreatment with softening agents of strengths diiferent from thatused in the final softening treatment, as is described in U. S. application S. No. 638,776 filed 20th October, 1932. The process of the present invention may be employed in connection with any one or more of such softening treatments.
Instead of carrying out the process of the present invention on the materials during their travel from one point to another, they may if desired,
. ethers of all kinds, for instance cellulose formate,
propionate, butyrate, nitro-acetate', or mixed cellulose esters and cellulose esters including higher fatty acid radicles, for instance the laurate radicle, or cellulose ethers, for instance ethyl or I necessary to produce that saponification.
benzyl celluloses, or unsaturated cellulose ethers or mixed ethers, for instance the mixed ethyl benzyl cellulose or mixed ether-esters of cellulose, e. g. ethyl cellulose acetate and oxyethyl cellulose acetate. The esters or ethers may be of lowfmedium or high viscosity characteristics; for instance cellulose acetates having a viscosity of 5-10, 20-30 or-50-100 or 200 or more as measured by comparing the viscosity of a 6% solution in acetone against a standard of glycerine taken as may be present in the materials. The
' yarns or other materials may consist wholly of the cellulose ester or ether or may contain other materials not deleteriously affected by the treatment.
Continuously with the stretching according to the present invention cellulose ester materials may be subjected to a. saponification which may be superficial, may be partial and uniform or may be complete. Such saponification may take place immediately after the stretching treatment of the present invention, or, particularly where the cellulose esters are subjected to a partial and substantially uniform saponification, may immediately precede the stretching treatment. The saponification may be effected with the aid of aqueous or aqueous alcoholic or alcoholic caustic soda, caustic potash, trisodium phosphate or other alkaline salt or reagent or may be effected with ammonia or organic amine in the vapour state. The saponifying media may contain sodium acetate or soaps or other buffer substances and may contain in addition to or in place of methyl alcohol or ethyl alcohol lime or other substances whereby the amount of caustic soda necessary for effecting any desired degree of saponification may be less than that theoretically Such processes are described in U. S. application S. No. 655,778 filed February 8, 1933. As described in U. S. application S. No. 668,068 filed on even date herewith the saponifying media may themselves contain oils or fats as with the stretching media of the present invention.
The following examples are given in order to illustrate the invention but it is to be clearly understood that they do not limit it in any way:--
Example 1 A cellulose acetate yarn in hank form is softened in a bath consisting of an emulsion of linseed oil in aqueous ethyl lactate prepared e. g. in the following manner. 8 parts of oleic acid, 2 parts of tri-ethanolamine and 30 parts of linseed oil are thoroughly mixed at ordinary temperatures and 30 parts of 50% aqueous ethyl lactate are then slowly added to the mixture with constant. and vigorous stirring until an emulsion is obtained. A further 60 parts of linseed oil are then added in small proportions with continual stirring. The emulsion is then diluted to 10 times its volume with 50% ethyl lactate which is added in small proportions at the beginning with constant stirring and then in larger amounts until the whole has been introduced and a satisfactory emulsion is obtained.
The hanks are soaked in the emulsion for about 5-l0 minutes at 20-25 C. and then stretched, for example by 100 to 200% of their original length and are found to have an increased tenacity.
Example 2 A number of cellulose acetate threads are taken from a creel of bobbins and led over a roller in warp formation into a stretching bath consisting of a 45-50% solution of dioxane containing 1 to 2% of the sodium salt of the sulphuric ester of lauryl alcohol. From the feed roller the warp passes through a reed to keep the threads apart, under a guide and then down the bath which is 80 to 100 feet long, through a; reed at the further end, round a draw-roller and then to washing, drying and winding devices. The peripheral speed of the feed roller is about 5 to 7 metres per minute while that of the draw-roller is 20 to 30 metres per minute so that a stretch of 400 to 500% is obtained. The temperature-of the bath is 20 to 25 C. The threads which have been stretched according to the example are found to have considerably greater tenacity than before stretching.
Example 3 A 25% solution of cellulose acetate in acetone 'is extruded into a coagulating bath consisting of example 1 to 1.5. After passing over a drawroller the filaments are washed to remove excess solvent, preferably with solutions of solvent in lower concentration or with salt solutions and are then dried and wound. Materials having an improved tenacity are thus obtained.
The term swelling agent as employed hereinafter in the claims is to be understood as including not only agents which exert only a swelling action on the cellulose derivative, but also agents which are true solvents therefor.
What I claim and desire to secure by Letters Patent -is:'
1. In a process for softening and stretching artificial filaments, threads, yarns, ribbons and likematerials containing organic derivatives of cellulose, the steps of softening the materials with a medium throughout which are uniformly distributed a swelling agent for the derivative. of cellulose and a substance selected from the group consisting of oils, fats and soaps and stretching the materials.
2. In a process for softening and stretching artificial filaments, threads, yarns, ribbons and formly distributed a swelling agent for cellulose acetate and a substance selected from the group consisting ofoils, fats and soaps and stretching the materials.
3. Process for the manufacture of high tenacity filaments, threads, yarns, ribbons and like materials containing cellulose acetate, which comprises forming the materials by extruding a suitable solution of cellulose acetate into an aqueous medium throughout which are uniformly distributed a swelling agent for cellulose acetate'and a substance selected from the group consisting of oils, fats and soaps; and stretching the materials during their formation.
4. In a process for softening and stretching artificial filaments, threads, yarns, ribbons and like materials containing organic derivatives of cellulose, the steps of softening the fully-formed materials with an aqueous medium in which are dissolved a swelling agent for the derivative of cellulose and a substance selected from the group consisting of oils, fats and soaps, and stretching v I solved a swelling agent for the cellulose derivative and a substance selected from the group con: sisting of oils, fats and soaps, and stretching the materials during their formation.
6. In a process for softening and stretching artificial filaments, threads, yarns, ribbons and likematerials containing cellulose acetate, the steps of softening the fully-formed materials with an aqueous medium in which are dissolved a swelling agent for cellulose acetate and a substance selected from the group consisting of oils, fats and soaps, and stretching the materials.
7. Process for the manufacture of high tenacity filaments, threads, yarns, ribbons and like materials containing cellulose acetate, which comprises forming the materials by extruding a suitable solution of cellulose acetate into an aqueous medium in which are dissolved a swelling agent for cellulose acetate and a substance selected from the group consisting of oils, fats and soaps, and stretching the materials during their formation.
8. In a process for softening and stretching artificial filaments, threads, yarns, ribbons and likematerials containingcellulose acetate, the steps of softening the fully-formed materials with an aqueous medium in which are dissolved dioxaneand a substance selected from the group consisting of oils, fats and soaps, and stretching the materials.
HENRY DREYFUS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB13145/32A GB403072A (en) | 1932-05-06 | 1932-05-06 | Improvements in the treatment of fibres or like materials of cellulose esters or ethers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2061565A true US2061565A (en) | 1936-11-24 |
Family
ID=10017672
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US668069A Expired - Lifetime US2061565A (en) | 1932-05-06 | 1933-04-26 | Treatment of fibers or like materials |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US2061565A (en) |
| FR (1) | FR754685A (en) |
| GB (1) | GB403072A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2925641A (en) * | 1956-02-09 | 1960-02-23 | Deering Milliken Res Corp | Method for processing cellulose ester yarns |
| US3220872A (en) * | 1961-05-01 | 1965-11-30 | Yokohama Rubber Co Ltd | Treated polyamide synthetic fibers for adherence to rubber materials |
| US4273739A (en) * | 1979-07-12 | 1981-06-16 | The United States Of America As Represented By The Secretary Of The Navy | Method of deforming thermoplastic polymers using ammonia as a reversible plasticizer |
-
1932
- 1932-05-06 GB GB13145/32A patent/GB403072A/en not_active Expired
-
1933
- 1933-04-24 FR FR754685D patent/FR754685A/en not_active Expired
- 1933-04-26 US US668069A patent/US2061565A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2925641A (en) * | 1956-02-09 | 1960-02-23 | Deering Milliken Res Corp | Method for processing cellulose ester yarns |
| US3220872A (en) * | 1961-05-01 | 1965-11-30 | Yokohama Rubber Co Ltd | Treated polyamide synthetic fibers for adherence to rubber materials |
| US4273739A (en) * | 1979-07-12 | 1981-06-16 | The United States Of America As Represented By The Secretary Of The Navy | Method of deforming thermoplastic polymers using ammonia as a reversible plasticizer |
Also Published As
| Publication number | Publication date |
|---|---|
| GB403072A (en) | 1933-12-06 |
| FR754685A (en) | 1933-11-10 |
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