US2085014A - Textile process and product - Google Patents
Textile process and product Download PDFInfo
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- US2085014A US2085014A US697926A US69792633A US2085014A US 2085014 A US2085014 A US 2085014A US 697926 A US697926 A US 697926A US 69792633 A US69792633 A US 69792633A US 2085014 A US2085014 A US 2085014A
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- United States
- Prior art keywords
- cellulose
- wax
- filaments
- yarns
- yarn
- 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
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- 238000000034 method Methods 0.000 title description 6
- 239000004753 textile Substances 0.000 title description 3
- 229920002678 cellulose Polymers 0.000 description 16
- 239000001913 cellulose Substances 0.000 description 15
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 235000014113 dietary fatty acids Nutrition 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- 229930195729 fatty acid Natural products 0.000 description 8
- 229920002301 cellulose acetate Polymers 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- -1 fatty acid glycol oleate Chemical class 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000009987 spinning Methods 0.000 description 5
- 235000011187 glycerol Nutrition 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- PWVUXRBUUYZMKM-UHFFFAOYSA-N 2-(2-hydroxyethoxy)ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOCCO PWVUXRBUUYZMKM-UHFFFAOYSA-N 0.000 description 3
- 239000012237 artificial material Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 229920003086 cellulose ether Polymers 0.000 description 2
- 238000000578 dry spinning Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229940095098 glycol oleate Drugs 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229940049964 oleate Drugs 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- ICLYJLBTOGPLMC-KVVVOXFISA-N (z)-octadec-9-enoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCC\C=C/CCCCCCCC(O)=O ICLYJLBTOGPLMC-KVVVOXFISA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- KQHZEKNQJJSVDN-KVVVOXFISA-N 2-(2-hydroxyethylamino)ethanol;(z)-octadec-9-enoic acid Chemical compound OCCNCCO.CCCCCCCC\C=C/CCCCCCCC(O)=O KQHZEKNQJJSVDN-KVVVOXFISA-N 0.000 description 1
- RZEWIYUUNKCGKA-UHFFFAOYSA-N 2-(2-hydroxyethylamino)ethanol;octadecanoic acid Chemical compound OCCNCCO.CCCCCCCCCCCCCCCCCC(O)=O RZEWIYUUNKCGKA-UHFFFAOYSA-N 0.000 description 1
- RMLRKDHXZUVGCH-KTKRTIGZSA-N 2-[2-(2-hydroxyethoxy)ethoxy]ethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCOCCOCCO RMLRKDHXZUVGCH-KTKRTIGZSA-N 0.000 description 1
- XOSCOJBBKOVIOM-UHFFFAOYSA-N 2-aminoethanol;octadecanoic acid Chemical compound NCCO.CCCCCCCCCCCCCCCCCC(O)=O XOSCOJBBKOVIOM-UHFFFAOYSA-N 0.000 description 1
- CGYGETOMCSJHJU-UHFFFAOYSA-N 2-chloronaphthalene Chemical compound C1=CC=CC2=CC(Cl)=CC=C21 CGYGETOMCSJHJU-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- KGWDUNBJIMUFAP-KVVVOXFISA-N Ethanolamine Oleate Chemical compound NCCO.CCCCCCCC\C=C/CCCCCCCC(O)=O KGWDUNBJIMUFAP-KVVVOXFISA-N 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
- DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- FVFJGQJXAWCHIE-UHFFFAOYSA-N [4-(bromomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CBr)C=C1 FVFJGQJXAWCHIE-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 230000009286 beneficial effect Effects 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
- 239000004327 boric acid Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 239000012185 ceresin wax Substances 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 239000001761 ethyl methyl cellulose Substances 0.000 description 1
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 229960005068 monoethanolamine oleate Drugs 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- ZHALDANPYXAMJF-UHFFFAOYSA-N octadecanoate;tris(2-hydroxyethyl)azanium Chemical compound OCC[NH+](CCO)CCO.CCCCCCCCCCCCCCCCCC([O-])=O ZHALDANPYXAMJF-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 229940117013 triethanolamine oleate Drugs 0.000 description 1
- 229940029614 triethanolamine stearate Drugs 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 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 textiles, films, etc. formed from a solution of a derivative of cellulose having incorporated therein an ingredient which does not adversely affect the solution from which filaments of good cross-section and better films may be formed.
- An object of the invention is the production of improved artificial material bearing derivatives of cellulose as a basis.
- Another object of the invention is the production of improved staple fibres.
- This invention is applicable to the formation of a yarn comprising substantially continuous filaments. It is of particular application to the 25 formation of relatively short lengths or staples which may be associated together by twisting to form spun yarn.
- the yarn made according to this invention is easily delustered and forms a soft crinkly fila- 30 ment especially adapted to spinning as staple yarns, i. e. a yarn composed of twisted short filaments.
- synthetic filaments can be spun to a crinkly fiber with a lower concen- 5 tration of dope.
- our invention permits the dry spinning of filaments of good cross-sections even at high concentrations of vapors of acetone or other solvent in the spinning cabinet.
- the yarn spun according to our invention has a very slightly subdued lustre and an appearance more like that of real silk than normally spun yarn.
- a great advantage in our invention is that when yarn made according thereto is delustered 45 it becomes very woolly and crinkled and delusters very heavily.
- This invention is applicable to the formation of yarns or filaments, under which terms are included, threads, assemblies or bundles of a num- 50 her of continuous filaments which may be in parallel relationship or which may be twisted together, artificial bristles, straws, short lengths of staple fibres or yarn spun from such staple fibres. It is also applicable to the formation of other arti- 55 ficial products such as foils, films and the like.
- This invention is particularly of importance in connection with the formation of artificial materials made of or containing organic derivatives of cellulose such as organic esters of cellulose and-cellulose ethers.
- organic esters are cellulose acetate, cellulose formate, cellulose 'propionate and cellulose butyrate
- examples of cellulose ethers are ethyl cellulose, methyl cellulose and benzyl cellulose.
- the yarns may have applied, thereto or incorporated therein effect materials such as pigments, filling materials, dyes, lakes, etc., fire retardants such as beta chloronaphthalene, triphenyl phosphate or tricresyl phosphate either in a coating material or in the yarns or filaments or both.
- effect materials such as pigments, filling materials, dyes, lakes, etc.
- fire retardants such as beta chloronaphthalene, triphenyl phosphate or tricresyl phosphate either in a coating material or in the yarns or filaments or both.
- the wax-like body contains at least a proportion of one or more such ingredients as mono-stearate of diethylene glycol, mono-stearate of ethylene glycol, the mono-stearate of triethylene glycol, the monoor di-stearate of glycerol, triethanolamine stearate, diethanolamine stearate, mono ethanolamine stearate, ammonium oleate, ethylene glycol oleate, diethylene glycol oleate, triethylene glycol oleate, the monoor di-oleate of glycerol, triethanolamine oleate, diethanolamine oleate, monoethanolamine oleate or other like waxy bodies.
- the palmitic or other monofatty acid ethers or esters 'of glycols, polyglycols, glycerols and higher polyhydric alcohols may be used.
- the wax-like bodies may be used alone or in combination with such ingredients as cresylic acid, butyl acetate, polymerized .fatty acid and glyceroor glyco-boric acid or cetyl alcohol or esters or ethers of higher fatty alcohols.
- any or a mixture of the above named wax-like bodies a proportion of the so-called non-emulsifiable wax -like bodies to act as sizes, hardeners, etc. such as ceresin wax, beeswax, stearic acid, stearin, palmitic acid, ozokerite wax, camauba wax, chlorinated naphthas and like bodies.
- the wax-like body or mixture of such bodies may be added to the dope in amoimts of 1% up the derivative of cellulose present, depending grams of soap per litre at on the mixture used. Certain of the mixtures raise the viscosity of the dope to such an extent that heated filtration is required. The percent of the wax-like material to be added depends also on the solubility of the material in the dope and will vary with the process used.
- the yarn delustersslightly in minutes when treated with an aqueous solution containing 2 65 C. while yarn formed from a solution of cellulose acetate not containing the diethylene glycol stearate is not afiected.-
- yarn formed from a solution of cellulose acetate not containing the diethylene glycol stearate is not afiected.
- Example II The process of Example I is carried out except that diethylene ilar results.
- Example III Example I is repeated except glycerol is used giving approxresults.
- Example IV Example II is repeated except mixture of equal parts of distearate and triethanolamine giving approximately the same Theprocess of that distearate of imateiy the same The process of that 5% of a ethylene glycol stearate, is used results.
- Yarns and staple fibres having a basis of organic derivatives of cellulose and containing readily emulsifiable wax-like higher fatty acid esters of polyhydrie alcohols.
- Yarns and staple fibres having a basis ofwe desire organic derivatives of cellulose and containing cellulose acetate and containing higher fatty acid esters of diethylene glycol.-
- Yarns and staple fibres having a basis of organic derivatives wax-like higher fatty acid alcohols, said esters containing only carbon, hydrogen and oxygen.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Patented June 29, 1937 TEXTILE PROCESS AND PRODUCT Camille Dreyfus, New York, N. Y., and William Whitehead, Cumberland, Md., assignors to Celanese Corporation of America, a corporation of Delaware N Drawing. Application November 14, 1933, Serial'No. 697,926. Renewed January 2, 1937 13 Claims.
This invention relates to textiles, films, etc. formed from a solution of a derivative of cellulose having incorporated therein an ingredient which does not adversely affect the solution from which filaments of good cross-section and better films may be formed. This application is a continuation-in-part of our application S. No. 3l8,583,'filed November 10, 1928, which has issued as Patent No. 1,958,283;
An object of the invention is the production of improved artificial material bearing derivatives of cellulose as a basis. Another object of the invention is the production of improved staple fibres. Other objectswill be apparent from the following description.
We have found that if yarns, filaments, films, foilsor other artificial materials are formed from solutions of derivatives of cellulose containing wax-like bodies which are preferably emulsified 20 in water the resulting product has many advantageous properties.
This invention is applicable to the formation of a yarn comprising substantially continuous filaments. It is of particular application to the 25 formation of relatively short lengths or staples which may be associated together by twisting to form spun yarn.
' The yarn made according to this invention is easily delustered and forms a soft crinkly fila- 30 ment especially adapted to spinning as staple yarns, i. e. a yarn composed of twisted short filaments.
With our invention synthetic filaments can be spun to a crinkly fiber with a lower concen- 5 tration of dope. In spinning filaments from cellulose acetate our invention permits the dry spinning of filaments of good cross-sections even at high concentrations of vapors of acetone or other solvent in the spinning cabinet.
40 The yarn spun according to our invention has a very slightly subdued lustre and an appearance more like that of real silk than normally spun yarn. A great advantage in our invention is that when yarn made according thereto is delustered 45 it becomes very woolly and crinkled and delusters very heavily.
This invention is applicable to the formation of yarns or filaments, under which terms are included, threads, assemblies or bundles of a num- 50 her of continuous filaments which may be in parallel relationship or which may be twisted together, artificial bristles, straws, short lengths of staple fibres or yarn spun from such staple fibres. It is also applicable to the formation of other arti- 55 ficial products such as foils, films and the like.
This invention is particularly of importance in connection with the formation of artificial materials made of or containing organic derivatives of cellulose such as organic esters of cellulose and-cellulose ethers. Examples of cellulose esters are cellulose acetate, cellulose formate, cellulose 'propionate and cellulose butyrate, while examples of cellulose ethers are ethyl cellulose, methyl cellulose and benzyl cellulose.
The yarns may have applied, thereto or incorporated therein effect materials such as pigments, filling materials, dyes, lakes, etc., fire retardants such as beta chloronaphthalene, triphenyl phosphate or tricresyl phosphate either in a coating material or in the yarns or filaments or both.
We preferably incorporate in the spinning solution a wax-like body which is emulsifiable in water, soapsolutions, solvents and like scouring baths. The wax-like body contains at least a proportion of one or more such ingredients as mono-stearate of diethylene glycol, mono-stearate of ethylene glycol, the mono-stearate of triethylene glycol, the monoor di-stearate of glycerol, triethanolamine stearate, diethanolamine stearate, mono ethanolamine stearate, ammonium oleate, ethylene glycol oleate, diethylene glycol oleate, triethylene glycol oleate, the monoor di-oleate of glycerol, triethanolamine oleate, diethanolamine oleate, monoethanolamine oleate or other like waxy bodies.
In place of or with the stearates and oleates above specified, the palmitic or other monofatty acid ethers or esters 'of glycols, polyglycols, glycerols and higher polyhydric alcohols may be used.
The wax-like bodies may be used alone or in combination with such ingredients as cresylic acid, butyl acetate, polymerized .fatty acid and glyceroor glyco-boric acid or cetyl alcohol or esters or ethers of higher fatty alcohols.
Beneficial results may be obtained by incorporating in the treating material mixtures of two or more of the above named or like ingredients as will be seen from a further description of my invention.
For certain purposes it is advisable to add to any or a mixture of the above named wax-like bodies a proportion of the so-called non-emulsifiable wax -like bodies to act as sizes, hardeners, etc. such as ceresin wax, beeswax, stearic acid, stearin, palmitic acid, ozokerite wax, camauba wax, chlorinated naphthas and like bodies.
The wax-like body or mixture of such bodies may be added to the dope in amoimts of 1% up the derivative of cellulose present, depending grams of soap per litre at on the mixture used. Certain of the mixtures raise the viscosity of the dope to such an extent that heated filtration is required. The percent of the wax-like material to be added depends also on the solubility of the material in the dope and will vary with the process used.
By way of describing our invention still further and not with the intention of limiting its scope thereby, we give the following specific examples- Eaxample I To a spinning solution acetone there is added 5% diethylene glycol stearate based upon acetate. The diethylene glycol stearate is added in a hot solution of acetone. The dry spinning stability of the charge is good and may be spun to form yarn of 150 denier 40 filaments. The cross section of the filaments is 100% bulbous and of a squat type. The yarn spun has a very slightly subdued lustre and an appearance much like that of real silk.
The yarn delustersslightly in minutes when treated with an aqueous solution containing 2 65 C. while yarn formed from a solution of cellulose acetate not containing the diethylene glycol stearate is not afiected.- When delustered for 30 minutes in an aqueous solution containing 2 grams'of soap per liter at 95 0., it becomes very woolly and crinkled and delusters very heavily while a blank takes on a moderate delustre.
Example II The process of Example I is carried out except that diethylene ilar results. I
Example III Example I is repeated except glycerol is used giving approxresults.
Example IV Example II is repeated except mixture of equal parts of distearate and triethanolamine giving approximately the same Theprocess of that distearate of imateiy the same The process of that 5% of a ethylene glycol stearate, is used results.
In all the processes of f the above examples gave a filament of good cross-section and this is probably due to the Wax-like body coming out of of cellulose acetate in I the weight of cellulose higher fatty acid glycol oleate is used giving sim- I departing from the" spirit of our invention.
Having described our invention, what to secure by Letters Patent is:
1. Yarns and staple fibres of cellulose acetate containing diethylene glycol steal-ate.
2. Artificial products having a basis of organic derivatives of cellulose and containing wax-like higher fatty acid esters of polyhydric alcohols. I
3. Yarns and staple fibres having a basis of organic derivatives of cellulose and containing readily emulsifiable wax-like higher fatty acid esters of polyhydrie alcohols.
4. Yarns and cellulose acetate fiable wax-like high-er fatty acid esters of polyhydric alcohols.
5. Yarns and staple fibres having a basis ofwe desire organic derivatives of cellulose and containing cellulose acetate and containing higher fatty acid esters of diethylene glycol.-
7. Artificial productshaving a basis of organic derivatives of cellulose and containing wax-like higher fatty acids with polyhydric alcohols.
drogen and oxygen. r
12. Yarns and staple fibres having a basis of organic derivatives wax-like higher fatty acid alcohols, said esters containing only carbon, hydrogen and oxygen.
13. Yarns and staple fibres having a basis of CAMILLE DREYF'US. WILLIAM WI -IITEHEAD.
of cellulose and containing
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US697926A US2085014A (en) | 1928-11-10 | 1933-11-14 | Textile process and product |
| GB3276434A GB434858A (en) | 1933-11-14 | 1934-11-14 | Improvements in the manufacture of artificial staple fibres |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US318583A US1958238A (en) | 1928-11-10 | 1928-11-10 | Spinning of artificial filaments |
| US357878A US2065517A (en) | 1928-11-10 | 1929-04-24 | Spinning of artificial filaments |
| US692428A US2085013A (en) | 1928-11-10 | 1933-10-06 | Cellulose derivative spinning solution containing wax |
| US697926A US2085014A (en) | 1928-11-10 | 1933-11-14 | Textile process and product |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2085014A true US2085014A (en) | 1937-06-29 |
Family
ID=31999547
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US697926A Expired - Lifetime US2085014A (en) | 1928-11-10 | 1933-11-14 | Textile process and product |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2085014A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2495714A (en) * | 1944-12-13 | 1950-01-31 | Baker Caster Oil Company | Cellulose derivative plasticized with an oily diester of a polyhydric alcohol |
| US2891089A (en) * | 1955-12-30 | 1959-06-16 | Sun Oil Co | Mixed esters of polyhydric alcohols with naphthenic and lower fatty acids |
-
1933
- 1933-11-14 US US697926A patent/US2085014A/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2495714A (en) * | 1944-12-13 | 1950-01-31 | Baker Caster Oil Company | Cellulose derivative plasticized with an oily diester of a polyhydric alcohol |
| US2891089A (en) * | 1955-12-30 | 1959-06-16 | Sun Oil Co | Mixed esters of polyhydric alcohols with naphthenic and lower fatty acids |
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