US2118840A - Production of textile threads and fabrics - Google Patents
Production of textile threads and fabrics Download PDFInfo
- Publication number
- US2118840A US2118840A US81264A US8126436A US2118840A US 2118840 A US2118840 A US 2118840A US 81264 A US81264 A US 81264A US 8126436 A US8126436 A US 8126436A US 2118840 A US2118840 A US 2118840A
- Authority
- US
- United States
- Prior art keywords
- threads
- thread
- cellulose acetate
- crepe
- shrinking
- 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
- 239000004744 fabric Substances 0.000 title description 16
- 238000004519 manufacturing process Methods 0.000 title description 15
- 239000004753 textile Substances 0.000 title description 2
- 239000003795 chemical substances by application Substances 0.000 description 48
- 229940081735 acetylcellulose Drugs 0.000 description 41
- 229920002301 cellulose acetate Polymers 0.000 description 39
- 238000000034 method Methods 0.000 description 16
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 235000019441 ethanol Nutrition 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 229920002678 cellulose Polymers 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 235000010980 cellulose Nutrition 0.000 description 6
- 150000002334 glycols Chemical class 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 238000004804 winding Methods 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 230000001747 exhibiting effect Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 229920000875 Dissolving pulp Polymers 0.000 description 2
- 235000011054 acetic acid Nutrition 0.000 description 2
- 229920003086 cellulose ether Polymers 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-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
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 239000004627 regenerated cellulose Substances 0.000 description 2
- 230000002522 swelling effect Effects 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 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
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
- ZAMLGGRVTAXBHI-UHFFFAOYSA-N 3-(4-bromophenyl)-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid Chemical compound CC(C)(C)OC(=O)NC(CC(O)=O)C1=CC=C(Br)C=C1 ZAMLGGRVTAXBHI-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
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 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
- 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
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical class [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 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
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- YSAVZVORKRDODB-WDSKDSINSA-N diethyl tartrate Chemical compound CCOC(=O)[C@@H](O)[C@H](O)C(=O)OCC YSAVZVORKRDODB-WDSKDSINSA-N 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229940116333 ethyl lactate Drugs 0.000 description 1
- 235000010944 ethyl methyl cellulose Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000001087 glyceryl triacetate Substances 0.000 description 1
- 235000013773 glyceryl triacetate Nutrition 0.000 description 1
- VHHHONWQHHHLTI-UHFFFAOYSA-N hexachloroethane Chemical compound ClC(Cl)(Cl)C(Cl)(Cl)Cl VHHHONWQHHHLTI-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- JCZMXVGQBBATMY-UHFFFAOYSA-N nitro acetate Chemical compound CC(=O)O[N+]([O-])=O JCZMXVGQBBATMY-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- BNIXVQGCZULYKV-UHFFFAOYSA-N pentachloroethane Chemical compound ClC(Cl)C(Cl)(Cl)Cl BNIXVQGCZULYKV-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229950011008 tetrachloroethylene Drugs 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 229960002622 triacetin Drugs 0.000 description 1
- 238000002166 wet spinning Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 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
- D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
- D01F11/02—Chemical after-treatment of artificial filaments or the like during manufacture of cellulose, cellulose derivatives, or proteins
Definitions
- Patented 3i 1938 PRODUCTION 01F TEX'lllllLlE THREADS AND lFAilBlltlllUS Henry lllreyfus, London, England No Drag. Application May 22, 1936, Serial No. 81,264. In Great Britain June 8, 1935 6 Claims.
- This invention relates to the manufacture of crepe twisted threads of cellulose esters or ethers.
- the invention is especially concerned with the production of crepe twisted threads of cellulose acetate, and will be more particularly described with reference to the production of such threads.
- crepe twisted cellulose acetate threads The production of commercially useful crepe twisted cellulose acetate threads is a matter involving considerable dimculty. threads of regenerated cellulose, commercially useful crepe threads can readily be obtained by applying a crepe twist of much the same order as that commonly used in the case of natural silk. The precise degree of twist desirable depends upon the denier of the thread and the number of its constituent filaments. In the case of cellulose acetate threads, however, very much higher twists are necessary and special twisting methods must be employed, both to obtain the desired crping power and to produce threads of sufficient strength for commercial purposes. British Patents Nos. 437,019, 438,590 and 438,591 describe methods whereby crepe-twisted cellulose acetate threads of very good strength and creping power may be obtained.
- crepe-twisted cellulose acetate threads of good strength and creping power may be prepared by the action of shrinking agents on threads of substantially lower twist than that required in the final thread.
- shrinking agents Bysubjecting to the action of shrinking agents a cellulose acetate thread having a certain humber of turns per inch twist, a thread having a greater number of turns per inch may be obtained.
- the final twist, after the subjecting to the action of the shrinking agent should not be below a certain minimum, depending upon the denier of the crepe twigted thread.
- This desirable minimum is of the order of '70 to '75 turns per inch in the case of threads of about 165 denier, and to turns per inch in the case of threads of about denier.
- crepe-twisted threads of cellulose acetate having these desirable twists and exhibiting good crping power may be obtained from threads having lower twists, for example twists lower by one fifth, one-quarter or one-third.
- shrinking agent an agent which is capable of effecting a shrinkage in length of filaments of the cellulose acetate of which the threads are made.
- the shrinking treatment is preferably effected by means of agents of such character and under such condi- In the case of tions as would shrink filaments of the cellulose acetate by about 10 to 30% of their length, for
- Agents which efiect a greater shrinkage may, however, be employed, though agents which are capable of effecting very high shrinkages, for example shrinkages of the order of 40, 50 or 60% frequently diminish the strength of the materials to'a substantial degree. Agents which are only capable .of shrinking to a comparatively low degree may be employed, but with the disadvantage that correspondingly smaller increases in the number of turns per unit length of the thread are obtained.
- the treatment with the shrinking agent should be effected under conditions permitting shrinkage of the threads treated, e. g. in the absence of any substantial thread tension.
- shrinking agents may be employed, for example inorganic swelling agents for cellulose acetate, such as aqueous solutions of alkali metal, alkaline earth metal, and ammonium thiocyanates.
- the shrinking agents employed are organic substances, mixtures of organic substances or solutions thereof, which have a substantial swelling action upon the cellulose acetate.
- the shrinking agent may, for example, consist of or comprise one or more of the following substances which have a swelling or solvent action upon cellulose acetate Alcohols, e. g. ethyl alcohol.
- Ketones for example diacetone alcohol and acetone.
- Monoand di-ethers of olefine glycols or polyolefine glycols e. g. the monoand di-methyl and ethyl ethers of ethylene glycol, the monomethyl and ethyl ethers of propylene glycol, and the mono-ethyl ether of diethylene glycol.
- Esters for example ethyl lactate or diethyl tartrate or esters of olefine glycols or polyolefine glycols, e. g. glycol mono-acetate, or esters of glycerol and other polyhydric alcohols, e. g. mono-, diand tri-acetin.
- Ether-esters of olefine glycols or poly-olefine glycols e. g. the acetate of glycol mono-ethyl ether.
- Cyclic ethers e. g. dioxane, methylene-ethylene-ether and other cyclic di-ethers.
- agents which at least at ordinary temperatures are incapable of dissolving cellulose acetate, but which are capable of swelling it to a high degree.
- agents for example methylene chloride, ethylene chloride, chloroform, tetrachlorethane, ethyl acetate and the like, usually become solvents forthe cellulose acetate when mixed with a comparatively small proportion of another liquid, particularly an alcohol such as ethyl alcohol.
- methylene chloride, chloroform, and tetrachlorethane when mixed with comparatively small proportions of alcohol, are capable of dissolving cellulose acetate.
- the methylene chloride, tetrachlorethane and the like are commonly referred to as latent solvents for the cellulose acetate and will be so referred to in this specification.
- the shrinking agent may consist of a single organic substance having a swelling action upon the cellulose acetate.
- another substance may, for example, be water, glycol, glycerol or other hydroxy compound.
- the shrinking may be eflected with the aid of aqueous ethyl alcohol, for example alcohol. of 50 to 80% strength, particularly alcohol of about 70% strength. In this way very considerable shrinkages may be produced.
- aqueous acetone e. g.. aqueous acetone of to 45% by volume
- aqueous dioxane e. g. aqueous dioxane of 38 to 43% by volume
- water-immiscible liquids as diluents or modifying agents for the organic swelling agents or latent solvents.
- water-immiscible diluents or modifying agents it is possible to secure good shrinkages and yet obtain products of good strength and/or extensibility.
- water-immiscible modifying agents or diluents may be mentioned benzene, toluene, xylene and other cyclic hydrocarbons, be he, petrol ether, kerosene and other hydrocarbons of the aliphatic series, and carbon tetrachloride, trichlor-ethylene, perchlorethylene, pentachlorethane, hexachlorethane, and other chlorinated or halogenated compounds which are substantially inert towards cellulose acetate.
- the diluent employed may be of relatively high boiling point, as is the case, for example, with tetrahydro naphthalene and decahydro naphthalene.
- Shrinking agents are conveniently used at ordinary temperatures. Other temperatures may be employed if desired according to the particular shrinking agent employed.
- the treatment of the twisted threads with the shrinking agent may be effected in various ways.
- the threads may be wound on supports which permit shrinkage of the thread, and thereafter immersed in the shrinking agent and the shrinking process allowed to take place.
- a more convenient method, however, is to subject running threads to the action of the: shrinking agent. This may be accomplished, for instance, by feeding the thread at a definite rate through a bath of the shrinking agent to a winding device where it is wound at a lower rate than the feed rate. The winding rate is adjusted according to the shrinkage which is required, Control of the feed rate may be efiected by mans of a pair of nip or feed rollers in the well known manner.
- the speed of the thread may be controlled by a further pair of nip or feed rollers preceding a suitable winding device.
- a suitable winding device itself, e. g. a drum winder, may be utilized directly to efiect the desired rate of winding.
- the shrinking agent When applying a shrinking agent to running threads in the aforesaid manner, it is desirable that the shrinking agent should be removed from the threads prior to rewinding. To this end the threads may be passed through a suitable dryer after treatment with the'shrinking agent.
- the shrinking agent treatment is in general most'conveniently applied as an operation distinct from the twisting of the yarn. If desired, however, the treatment with shrinking agent may be efiected on the running thread continuously with the twisting of the thread. Such a combined process may be carried out with the aid of a twisting spindle of the kind in which twist is inserted as the thread is drawn off from a rotating package.
- the twisted thread may be drawn oil by a pair of nip or feed rolls and led through a bath of shrinking agent or other device wherein treatment with shrinking agent is efiected, and the desired shrinkage allowed to take place. Any necessary drying and winding then follows, as in the case of treating running threads in an operation separate from twisting.
- the cellulose acetate threads treated in accordance with the invention may have been prepared by ordinary dry spinning from solutions of cellulose acetate. Again they may have been made by wet spinning processes or by stretching filaments of cellulose acetate, for example while in a softened state, as described for example in Patent No. 1,709,470 and British Patents Nos. 323,790, 370,430, 371,461, 438,584 and 438,586.
- the cellulose acetate threads to be treated with shrinking agents in accordance with the present invention may have had their twist inserted in a single stage or in two or more stages.
- the threads may, between stages of twisting, be subjected to a wetting or other treatment as described in British Patent No. 386,344, or to a steaming treatment as described in British Patent No. 386,374.
- the twisting may be effected in a manner commonly practised in the twisting of textile threads, or most advantageously, the threads may be twisted while under the influence of steam, preferably in the presence of moisture, or while under the influence of hot water, as described in British Patents Nos. 437,019, 438,590 and 438,591 in connection with the crpe twisting of cellulose acetate threads.
- the degree of twist of the cellulose acetate threads prior to the treatment with shrinking will, in general, be less than suffices to give the threads any substantial crping power, but usually at least 70% of that requisite for crping power.
- the twist may be less than a value determined according to the thread denier with shrinking agents may be utilized to enhance the crping power of threads already exhibiting substantial crping power, for example crpetwisted cellulose acetate threads produced by the methods described in the above-mentioned British Patents Nos. 437,019, 438,590 and 438,591.
- While the invention is of particular value in the production of threads having a twist sumcient to afford crping power, it may be utilized in the production of threads having substantial twists but less than is required in a crepe thread.
- cellulose acetate threads having a twist of 50 to 70 turns per inch or more may be produced by the action of shrinking agents on threads of lower twist than is required in the finished thread.
- the new method as compared with direct twisting to the required degree, enables improved results to be obtained as regards strength and other properties of the resultant threads.
- the threads may be made of filaments of cellulose formate, proplonate or butyrate, or of mixed esters of cellulose, e. g. cellulose nitro-acetate or cellulose acetate-butyrate.
- the threads may be of cellulose ethers e. g. methyl cellulose, ethyl cellulose or benzyl cellulose, or of ether-esters of cellulose, e. g. an esterified low ether of cellulose, or an acetylated or otherwise esterified hydroxy ethyl cellulose or other hydroxy alkyl cellulose.
- Crepe twisted and other threads produced in accordance with the invention may be incorporated in fabricsin the manner well known in the art of making crepe and other fabrics.
- a warp of cellulose acetate threads of low twist may be employed, the weft consisting of cellulose acetate crepe threads prepared in accordance with the present invention, pairs of picks of right-hand twisted threads alternating with pairs of picks of left-hand twisted threads.
- a hot aqueous treatment for example a hot soap treatment such as is commonly employed in the case of natural sillr crepe fabrics or regenerated cellulose crepe fabrics.
- the warp is of material which does not undergo substantial shrinkage under the action of the shrinking agent
- the warp threads alone may be spaced more widely than in similar fabrics designed to be crped without substantial shrinkage of the filaments of the threads.
- the warp, like the weft is of filaments which are shrunk by the action ofthe shrinking agent, then both warp and weft are advantageously more widely spaced.
- Process for the production of a highly twisted crepe thread of cellulose acetate filaments which comprises subjecting a cellulose acetate thread, having substantially no crping power but a twist of at least 70% of that required to impart crping power to the action of a shrinking agent so as to shrink the filaments of the thread to such a degree that creping power is imparted to the thread.
- Process for the production of a highly twisted crepe thread of cellulose acetate filaments which comprises twisting a cellulose acetate thread, while under the influence of steam under conditions such that moisture is present, to a power, and thereafter subjecting the threads to the action of a shrinking agent so as to shrink the filaments of the thread to such a degree asto impart crping power to the thread.
- Process for the production of a highly twisted crepe thread of cellulose acetate filaments which comprises twisting a cellulose acetate thread, whileunder the influence of a hot aqueous medi, to a twist insumcient to impart crtping power but at least 70% of that required to impart creping power, and thereafter shrinking the thread, sumcient to impart creping power thereto, by the action of a cold non aqueous shrinking agent capable of shrinking cellulose acetate filaments by from to 30% of their original length.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
Description
Patented 3i, 1938 PRODUCTION 01F TEX'lllllLlE THREADS AND lFAilBlltlllUS Henry lllreyfus, London, England No Drag. Application May 22, 1936, Serial No. 81,264. In Great Britain June 8, 1935 6 Claims.
This invention relates to the manufacture of crepe twisted threads of cellulose esters or ethers. The invention is especially concerned with the production of crepe twisted threads of cellulose acetate, and will be more particularly described with reference to the production of such threads.
The production of commercially useful crepe twisted cellulose acetate threads is a matter involving considerable dimculty. threads of regenerated cellulose, commercially useful crepe threads can readily be obtained by applying a crepe twist of much the same order as that commonly used in the case of natural silk. The precise degree of twist desirable depends upon the denier of the thread and the number of its constituent filaments. In the case of cellulose acetate threads, however, very much higher twists are necessary and special twisting methods must be employed, both to obtain the desired crping power and to produce threads of sufficient strength for commercial purposes. British Patents Nos. 437,019, 438,590 and 438,591 describe methods whereby crepe-twisted cellulose acetate threads of very good strength and creping power may be obtained.
I have found that valuable crepe-twisted cellulose acetate threads of good strength and creping power may be prepared by the action of shrinking agents on threads of substantially lower twist than that required in the final thread. Bysubjecting to the action of shrinking agents a cellulose acetate thread having a certain humber of turns per inch twist, a thread having a greater number of turns per inch may be obtained. In order that the resulting threads may have suficient crping power, it is preferable that the final twist, after the subjecting to the action of the shrinking agent, should not be below a certain minimum, depending upon the denier of the crepe twigted thread. This desirable minimum is of the order of '70 to '75 turns per inch in the case of threads of about 165 denier, and to turns per inch in the case of threads of about denier. By the new process crepe-twisted threads of cellulose acetate having these desirable twists and exhibiting good crping power may be obtained from threads having lower twists, for example twists lower by one fifth, one-quarter or one-third.
By the term shrinking agent is meant an agent which is capable of effecting a shrinkage in length of filaments of the cellulose acetate of which the threads are made. The shrinking treatment is preferably effected by means of agents of such character and under such condi- In the case of tions as would shrink filaments of the cellulose acetate by about 10 to 30% of their length, for
example 15 to 20 or 25% of their length. Agents which efiect a greater shrinkage may, however, be employed, though agents which are capable of effecting very high shrinkages, for example shrinkages of the order of 40, 50 or 60% frequently diminish the strength of the materials to'a substantial degree. Agents which are only capable .of shrinking to a comparatively low degree may be employed, but with the disadvantage that correspondingly smaller increases in the number of turns per unit length of the thread are obtained.
It is desirable that the treatment with the shrinking agent should be effected under conditions permitting shrinkage of the threads treated, e. g. in the absence of any substantial thread tension.
Various shrinking agents may be employed, for example inorganic swelling agents for cellulose acetate, such as aqueous solutions of alkali metal, alkaline earth metal, and ammonium thiocyanates. Preferably, however, the shrinking agents employed are organic substances, mixtures of organic substances or solutions thereof, which have a substantial swelling action upon the cellulose acetate. The shrinking agent may, for example, consist of or comprise one or more of the following substances which have a swelling or solvent action upon cellulose acetate Alcohols, e. g. ethyl alcohol.
Organic acids, for example acetic acid, formic acid and lactic acid. v
Ketones, for example diacetone alcohol and acetone.
Monoand di-ethers of olefine glycols or polyolefine glycols, e. g. the monoand di-methyl and ethyl ethers of ethylene glycol, the monomethyl and ethyl ethers of propylene glycol, and the mono-ethyl ether of diethylene glycol.
Esters, for example ethyl lactate or diethyl tartrate or esters of olefine glycols or polyolefine glycols, e. g. glycol mono-acetate, or esters of glycerol and other polyhydric alcohols, e. g. mono-, diand tri-acetin.
Ether-esters of olefine glycols or poly-olefine glycols, e. g. the acetate of glycol mono-ethyl ether.
Cyclic ethers, e. g. dioxane, methylene-ethylene-ether and other cyclic di-ethers. I
Phenols.
ylene.
It is especially advantageous to efiect the shrinking with the aid of agents which at least at ordinary temperatures are incapable of dissolving cellulose acetate, but which are capable of swelling it to a high degree. Such agents, for example methylene chloride, ethylene chloride, chloroform, tetrachlorethane, ethyl acetate and the like, usually become solvents forthe cellulose acetate when mixed with a comparatively small proportion of another liquid, particularly an alcohol such as ethyl alcohol. Thus, methylene chloride, chloroform, and tetrachlorethane, when mixed with comparatively small proportions of alcohol, are capable of dissolving cellulose acetate. The methylene chloride, tetrachlorethane and the like are commonly referred to as latent solvents for the cellulose acetate and will be so referred to in this specification.
As indicated above, the shrinking agent may consist of a single organic substance having a swelling action upon the cellulose acetate. Generally speaking, however, it is, found most convenient to modify the action of an organic swelling agent by admixture with another substance. Such other substance may, for example, be water, glycol, glycerol or other hydroxy compound. Thus, the shrinking may be eflected with the aid of aqueous ethyl alcohol, for example alcohol. of 50 to 80% strength, particularly alcohol of about 70% strength. In this way very considerable shrinkages may be produced. Again, aqueous acetic acid, aqueous diacetone alcohol,
aqueous acetone, e. g.. aqueous acetone of to 45% by volume, or aqueous dioxane, e. g. aqueous dioxane of 38 to 43% by volume, may be employed.
However it is preferred to employ water-immiscible liquids as diluents or modifying agents for the organic swelling agents or latent solvents. With such water-immiscible diluents or modifying agents it is possible to secure good shrinkages and yet obtain products of good strength and/or extensibility. As examples of such water-immiscible modifying agents or diluents may be mentioned benzene, toluene, xylene and other cyclic hydrocarbons, be he, petrol ether, kerosene and other hydrocarbons of the aliphatic series, and carbon tetrachloride, trichlor-ethylene, perchlorethylene, pentachlorethane, hexachlorethane, and other chlorinated or halogenated compounds which are substantially inert towards cellulose acetate. The diluent employed may be of relatively high boiling point, as is the case, for example, with tetrahydro naphthalene and decahydro naphthalene.
Excellent results may be obtained with a 55 to 70 or 75% solution of methylene chloride in benzene or a similar solution of ethyl acetate in benzene.
Shrinking agents are conveniently used at ordinary temperatures. Other temperatures may be employed if desired according to the particular shrinking agent employed.
The treatment of the twisted threads with the shrinking agent may be effected in various ways. Thus, the threads may be wound on supports which permit shrinkage of the thread, and thereafter immersed in the shrinking agent and the shrinking process allowed to take place. A more convenient method, however, is to subject running threads to the action of the: shrinking agent. This may be accomplished, for instance, by feeding the thread at a definite rate through a bath of the shrinking agent to a winding device where it is wound at a lower rate than the feed rate. The winding rate is adjusted according to the shrinkage which is required, Control of the feed rate may be efiected by mans of a pair of nip or feed rollers in the well known manner. Similarly, after the shrinkage treatment the speed of the thread may be controlled by a further pair of nip or feed rollers preceding a suitable winding device. itself, e. g. a drum winder, may be utilized directly to efiect the desired rate of winding.
When applying a shrinking agent to running threads in the aforesaid manner, it is desirable that the shrinking agent should be removed from the threads prior to rewinding. To this end the threads may be passed through a suitable dryer after treatment with the'shrinking agent.
The shrinking agent treatment is in general most'conveniently applied as an operation distinct from the twisting of the yarn. If desired, however, the treatment with shrinking agent may be efiected on the running thread continuously with the twisting of the thread. Such a combined process may be carried out with the aid of a twisting spindle of the kind in which twist is inserted as the thread is drawn off from a rotating package. The twisted thread may be drawn oil by a pair of nip or feed rolls and led through a bath of shrinking agent or other device wherein treatment with shrinking agent is efiected, and the desired shrinkage allowed to take place. Any necessary drying and winding then follows, as in the case of treating running threads in an operation separate from twisting.
The cellulose acetate threads treated in accordance with the invention may have been prepared by ordinary dry spinning from solutions of cellulose acetate. Again they may have been made by wet spinning processes or by stretching filaments of cellulose acetate, for example while in a softened state, as described for example in Patent No. 1,709,470 and British Patents Nos. 323,790, 370,430, 371,461, 438,584 and 438,586.
The cellulose acetate threads to be treated with shrinking agents in accordance with the present invention may have had their twist inserted in a single stage or in two or more stages. In the case oi. dior multi-stage twisting, the threads may, between stages of twisting, be subjected to a wetting or other treatment as described in British Patent No. 386,344, or to a steaming treatment as described in British Patent No. 386,374. The twisting may be effected in a manner commonly practised in the twisting of textile threads, or most advantageously, the threads may be twisted while under the influence of steam, preferably in the presence of moisture, or while under the influence of hot water, as described in British Patents Nos. 437,019, 438,590 and 438,591 in connection with the crpe twisting of cellulose acetate threads.
The degree of twist of the cellulose acetate threads prior to the treatment with shrinking If desired, however, the winding .device agents will, in general, be less than suffices to give the threads any substantial crping power, but usually at least 70% of that requisite for crping power. The twist may be less than a value determined according to the thread denier with shrinking agents may be utilized to enhance the crping power of threads already exhibiting substantial crping power, for example crpetwisted cellulose acetate threads produced by the methods described in the above-mentioned British Patents Nos. 437,019, 438,590 and 438,591.
While the invention is of particular value in the production of threads having a twist sumcient to afford crping power, it may be utilized in the production of threads having substantial twists but less than is required in a crepe thread. For example, cellulose acetate threads having a twist of 50 to 70 turns per inch or more (but less than is required for crepe purposes) may be produced by the action of shrinking agents on threads of lower twist than is required in the finished thread. The new method, as compared with direct twisting to the required degree, enables improved results to be obtained as regards strength and other properties of the resultant threads.
In place of cellulose acetate threads, crepe twisted and other highly twisted threads of other esters or ethers ofcellulose may be treated by the new process. Thus the threads may be made of filaments of cellulose formate, proplonate or butyrate, or of mixed esters of cellulose, e. g. cellulose nitro-acetate or cellulose acetate-butyrate. Again the threads may be of cellulose ethers e. g. methyl cellulose, ethyl cellulose or benzyl cellulose, or of ether-esters of cellulose, e. g. an esterified low ether of cellulose, or an acetylated or otherwise esterified hydroxy ethyl cellulose or other hydroxy alkyl cellulose.
Crepe twisted and other threads produced in accordance with the invention may be incorporated in fabricsin the manner well known in the art of making crepe and other fabrics. For example, for the production of a fabric of the crepe de Chine type, a warp of cellulose acetate threads of low twist may be employed, the weft consisting of cellulose acetate crepe threads prepared in accordance with the present invention, pairs of picks of right-hand twisted threads alternating with pairs of picks of left-hand twisted threads. To develop the crepe efiect the fabrics may be given a hot aqueous treatment, for example a hot soap treatment such as is commonly employed in the case of natural sillr crepe fabrics or regenerated cellulose crepe fabrics.
According to a further feature of my invention I apply the treatment with the shrinking agent to fabrics containing the twisted threads. In this way fabrics exhibiting crepe efiects may be obtained even when the twist of the threads is lnsufiicient to giverise to crepe efiects when the same fabric is subjected to hot aqueous treatment as in ordinary crepe practice. Where treatment with shrinking agents is applied to threads in a fabric it is advantageous that the fabric should have a rather more open construction than in the case of a fabric on which crepe eflect is to be developed solely by a hot aqueous treatment. For example, where the warp is of material which does not undergo substantial shrinkage under the action of the shrinking agent, the warp threads alone may be spaced more widely than in similar fabrics designed to be crped without substantial shrinkage of the filaments of the threads. Where, however, the warp, like the weft, is of filaments which are shrunk by the action ofthe shrinking agent, then both warp and weft are advantageously more widely spaced.
Having described my invention, what I desire to secure by Letters Patent is:
1. Process for the production of a highly twisted crepe thread of cellulose acetate filaments, which comprises subjecting a cellulose acetate thread, having substantially no crping power but a twist of at least 70% of that required to impart crping power to the action of a shrinking agent so as to shrink the filaments of the thread to such a degree that creping power is imparted to the thread.
2. Process for the production of a highly twlsted crepe thread of cellulose acetate filaments,
which comprises twisting a cellulose acetate thread, while under the influence of a hot aqueous medium, to a twist insumcient to impart creping power but at least 70% of that required to impart crping power, and thereafter subjecting the thread to the action of a shrinking agent so as to shrink the filaments of the thread to such a degree as to impart creping power to the thread.
3. Process for the production of a highly twisted crepe thread of cellulose acetate filaments, which comprises twisting a cellulose acetate thread, while under the influence of steam under conditions such that moisture is present, to a power, and thereafter subjecting the threads to the action of a shrinking agent so as to shrink the filaments of the thread to such a degree asto impart crping power to the thread.
4. Process for the production of a highly twisted crepe thread of cellulose acetate filaments, which comprises twisting a cellulose acetate thread, while under the influence of a hot aqueous medium, to a twist less than a value deter= mined according to the thread denier, said value being '70 turns per inch for threads of 165 denier and 85 turns per inch for threads of 115 denier, and thereafter shrinking the filaments of the thread until the number of turns per inch is greater than said value.
5. Process for the production of a highly twisted crepe thread of cellulose acetate filaments, which comprises twisting a cellulose acetate thread, whileunder the influence of a hot aqueous medi, to a twist insumcient to impart crtping power but at least 70% of that required to impart creping power, and thereafter shrinking the thread, sumcient to impart creping power thereto, by the action of a cold non aqueous shrinking agent capable of shrinking cellulose acetate filaments by from to 30% of their original length.
6. Process for the production of fabric exhibiting crepe efl'ects, which comprises twisting cellu lose acetate threads, while under the influence of a hot aqueous medium, up to a twist oi. at least '70 per cent but less than 100 per cent of that required to impart crping power, incorporating the threads in a fabric and subjecting the fabric to the action of a shrinking agent so
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2118840X | 1935-06-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2118840A true US2118840A (en) | 1938-05-31 |
Family
ID=10898977
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US81264A Expired - Lifetime US2118840A (en) | 1935-06-08 | 1936-05-22 | Production of textile threads and fabrics |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2118840A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2460875A (en) * | 1945-08-02 | 1949-02-08 | Celanese Corp | Combined dyeing and creping process for organic derivative of cellulose fabrics |
| US2976601A (en) * | 1955-10-07 | 1961-03-28 | Celanese Corp | Production of a cellulose staple fiber batting |
| US3210964A (en) * | 1960-12-02 | 1965-10-12 | Kellwood Co | Stretchable hosiery and the like |
-
1936
- 1936-05-22 US US81264A patent/US2118840A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2460875A (en) * | 1945-08-02 | 1949-02-08 | Celanese Corp | Combined dyeing and creping process for organic derivative of cellulose fabrics |
| US2976601A (en) * | 1955-10-07 | 1961-03-28 | Celanese Corp | Production of a cellulose staple fiber batting |
| US3210964A (en) * | 1960-12-02 | 1965-10-12 | Kellwood Co | Stretchable hosiery and the like |
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