US2394212A - Manufacture of artificial products - Google Patents
Manufacture of artificial products Download PDFInfo
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- US2394212A US2394212A US406187A US40618741A US2394212A US 2394212 A US2394212 A US 2394212A US 406187 A US406187 A US 406187A US 40618741 A US40618741 A US 40618741A US 2394212 A US2394212 A US 2394212A
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- Prior art keywords
- cellulose
- yarns
- ethylene oxide
- yarn
- polymers
- Prior art date
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- Expired - Lifetime
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- 238000004519 manufacturing process Methods 0.000 title description 5
- 229920000642 polymer Polymers 0.000 description 27
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 23
- 229920002678 cellulose Polymers 0.000 description 19
- 239000001913 cellulose Substances 0.000 description 19
- 239000004744 fabric Substances 0.000 description 17
- 239000000463 material Substances 0.000 description 17
- 229920002301 cellulose acetate Polymers 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000011888 foil Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000012736 aqueous medium Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000009941 weaving Methods 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 239000010902 straw Substances 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Natural products CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000000578 dry spinning Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000002895 organic esters Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229920008347 Cellulose acetate propionate Polymers 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- 102000018361 Contactin Human genes 0.000 description 1
- 108060003955 Contactin 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
- 239000005977 Ethylene Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Chemical class 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 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
- HKQOBOMRSSHSTC-UHFFFAOYSA-N cellulose acetate Chemical compound OC1C(O)C(O)C(CO)OC1OC1C(CO)OC(O)C(O)C1O.CC(=O)OCC1OC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(COC(C)=O)O1.CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 HKQOBOMRSSHSTC-UHFFFAOYSA-N 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000008241 heterogeneous mixture Substances 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000002166 wet spinning Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/50—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads
- D03D15/56—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads elastic
Definitions
- This invention relates to the manufacture of artificial products such as filaments, yarns,
- threads, films, foils, ribbons, straw, fibers, bristles and the like having a basis of an organic deriva'-' tive of cellulose.
- An object of our invention is to prepare artificial products such as filaments, yarns, threads, films, foils, ribbons, straws, bristles and the like which deluster readily and retain their delustered or opaque appearance permanently.
- Another object of our invention is the preparation of crepe yarns which when woven into fabrics produce improved crepe effects.
- Still another object of our invention is to improve the dyeing characteristics of yarns having a basis of an organic derivative of cellulose.
- organic derivative of cellulose yarns containing polymers of ethylene oxide have a considerably increased affinity for dyestuffs normally employed for dyeing organic derivative of cellulose materials and may be dyed in deeper shades by such dyestufis with less processing than yarns having a basis of an organic derivative of cellulose as heretofore prepared.
- This increased dyeing afiinity is not only achieved in yarns which have been delustered but, as stated, yarns in which the ethylene oxide polymer is still present likewise exhibit this desirable property.
- films or foils may be formed from solutions containing polymers of ethylene oxide, which films or foils, upon being given a delustering treatment, are permanently delustered.
- the polymers of ethylene oxide employed in accordance with our invention may be prepared in any suitable manner as by contactin liquid ethylene oxide at suitable temperatures with fullers 'earth or other similar material containing aluminum oxide.
- the products of polymerization are mixed polymers and may range from a syrupy liquid through waxy solids to rubbery compounds; By suitable treatment the polymers may be separated into several, fractions. Each of the several fractions contains polymers of different degrees of polymerization but of substantially similar or related characteristics.
- each fraction co tains polymers having degrees of polymerization different from those of the other fraction. While the heterogeneous mixture of polymers may be employed in our process prior to being separated into individual components, we preferably separate the mixture into its fractions and employ those fractions which are entirely water-soluble and fully compatible with the organic derivatives of cellulose employed. I
- the ethylene oxide polymers may be added in varying amounts to the solutions from which the yarns, filaments, films, foils or other plastic materials, and the like, may be prepared. We have found that excellent results may be achieved when from 1 to 50%, and preferably from 5 to 10%, of ethylene oxide .polymers, based on the weight of the organic derivative of cellulose contained therein, is added to the solutions from which the filaments, films, etc. are prepared.
- the solutions containing the ethylene oxide polymers after thorough mixing to obtain uniformity, may,be filtered and then extruded through the orifices of a spinneret either into an evaporative atmosphere as in dry spinning or into a coagulative medium as in wet spinning.
- Such solutions of the organic derivatives of cellulose material ranging in thickness the like, and the solvent evaporated therefrom.
- Filaments spun from solutions containing the ethylene oxide polymers may be the fine filaments having a denier of, say, 1 to 10, such as are used for making yarns, or they may be much heavie i. e. having adenier of, say, 50 to 2.000, which may be used for artificial bristles or, when flattened, may be used for artificial straw.
- Our invention may also be advantageously employed for making films, foils and other products where strength and delusterability are important.
- the solution of organic derivative of cellulose containing the polymers may from that of thin foil, to that of film and of sheets of substantial thickness.
- the delustering treatment is preferably carried out in hot aqueous media.
- water at elevated temperature makes an excellent delustering agent.
- Wet steam may also be employed.
- the aqueous delustering bath may also contain other substances such as soap. salts, acid salts, pine oil, tetralin, etc. which accelerate or enhance the delustering action of the bath. While we preferably employ these solutions at or near the boiling point, i. e. about 100 C., temperatures as low as 60 C. may be advantageously employed.
- While our invention is particularly applicable for the preparation of permanently delustered filaments, yarns, foils, films and other products having a basis of cellulose acetate, other organic derivatives of cellulose, such as other organic esters and ethers of cellulose, may be employed.
- organic esters of cellulose are cellulose propionate and cellulose butyrate andmixed esters such as cellulose acetate-propionate and cellulose acetate-butyrate, while examples of cellulose ethers are ethyl cellulose and benzyl cellulose.
- any suitable solvent in which both the organic derivatives of cellulose and the ethylene oxide polymers are soluble may be employed.
- Examples of such solvents are acetone, acetone and ethyl or methyl alcohol, chloroform, ethylene dichloride, ethylene dichloride and ethyl or By this treatment the yarn The depth of shade are considerably greater than that methyl alcohol, methylene chloride and ethyl or methyl alcohol, and ethylene formal.
- the resulting solution is thoroughly mixed and filtered and is then processed, employing a dry-spinning method, into a yarn of 124 denier having 60 filaments.
- the yarn thus prepared is backwound on to a stainless steel bobbin and the bobbin holding the yarn is then immersed in boiling water for 15 minutes and is then dried.
- the yarn produced is completely and permanently delustered and has a tenacity of 1.32 grams per denier. Pigmented yarn of the same denier and having the same number of filaments h a tenacity of only 1.05.
- Example I A film .0026 inch in thickness is poured or cast from the solution prepared as indicated in Exampie 1. This film is found to have a breaking strength of 5,700 pounds per square inch, an elongation of 6% and is transparent. After being treated in boiling water for 15 minutes the ethylene oxide polymer contained therein is removed, the film becoming completely opaque. The strength of the resulting opaque film, i. e. the breaking strength, is found to have risen to 6,700 lbs. per square inch and the elongation to 14.2%.
- Emmzlle III Yarn prepared in the manner indicated in Example I and still containing the ethylene oxide polymer therein is delustered by treatment for one hour at 98-100 C. in a bath containing 20 grams per liter of sodium oleate.
- the delustered yarn is then dyed for 30 minutes at C. in a bath containing 1% of lzl-dimethyl-aminoanthraquinone based on the weight of the yarn, 0.25 gram per liter of sodium oleate soap and 3 cos. per liter of Celascour (a mixture of Turkey red oil, xylene and water).
- the yarn is then rinsed well in water at 65 and then in cold water. is delustered and dyed a blue shade, the degree of delustering and depth of shade being greater than that produced on cellulose acetate yarn which is free from ethylene oxide polymer.
- Example IV Yarn prepared in the manner indicated in Example I, and while still containing the ethylene oxide polymer in the yarn structure, is treated in a bath comprising 1% of 1:4-dimethyl-aminoanthraquinone based on the weight of the yarn to be dyed, 0.25 gram per liter of sodium oleate soap and 3.0 ccs. per liter of Celascour.
- the yarn is immersed in the bath maintained at 98-100 C. for one hour.
- the yarn is simultaneously delustered and dyed a blue shade by this treatment. and degree of delustering achieved when cellulose acetate yarn not containing the ethylene oxide polymer is given a like treatment in the bath.
- Example V To a solution of 1 part by weight of cellulose acetate in 3 parts by weight of acetone is added 10% on the weight of cellulose acetate of ethylene oxide polymer melting at about 50 C. and having a molecular weight of about 4,000. The solution is mixed and filtered and is then dry spun into a yarn of 180 denier having 40 filaments. The resulting yarn is then given a crepe twist of 70 turns per inch during an up-twisting operation whilebeing subjected to the action of steam during the actual insertion of the twist. This crepe yarn is employed for weaving a crepe fabric having 74 picks per inch on a warp of 120 ends of a 100 denier, 40 filament cellulose acetate yarn of turns per inch. The original width of this fabric is 45 inches.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
I Patented Feb. 5, .1946
MANUFACTURE or An'rmrcm PRODUCTS Richard R. Sitzler and Joseph E. Bludworth,
Cumberland, Md., ,assignol's to Celanese Corporation of America, a corporation of Delaware No Drawing. Application August 9, 1941, Serial No. 406,187
3 Claims.
This invention relates to the manufacture of artificial products such as filaments, yarns,
threads, films, foils, ribbons, straw, fibers, bristles and the like having a basis of an organic deriva'-' tive of cellulose.
An object of our invention is to prepare artificial products such as filaments, yarns, threads, films, foils, ribbons, straws, bristles and the like which deluster readily and retain their delustered or opaque appearance permanently.
Another object of our invention is the preparation of crepe yarns which when woven into fabrics produce improved crepe effects.
Still another object of our invention is to improve the dyeing characteristics of yarns having a basis of an organic derivative of cellulose.
Other objects of our invention will appear from the followin detailed description.
Artificial filaments having a [basis of an organic derivative of cellulose have been prepared by extrusion of solutions of the cellulose derivatives in a volatile solvent through orifices of a spinneret into an evaporative atmosphere. Yarns made from filaments prepared in this way have found extensive use. While such yarns become del stered in y ng or scourin baths at elevated temperatures, they have a tendency to become relustered upon the application of heat and moisture as in ironing, or by treating the yarns with certain chemical agents. Yarns and films of apermanent dull finish have been obtained by incorporating certain pigments in the solutions from which the yarns are spun. but such pigmented yarns or films are lacking in strength and for this reason are limited in their uses. Due to this lack of strength pigmented yarns are of little value in the preparation of crepe yarns which. are to. be employed in the preparation of crepe fabrics.
We have now discovered that if polymers of ethylene oxide are added to the solutions employed for spinning yarns of an organic derivative of cellulose, there may be obtained yarns having excellent strength and improved creping properties. When yarns prepared in this manner are subjected to a. delustering treatment in aqueous media, the resulting yarns are permanently delustered and on subsequent treatment with agents which-normally r'eluster the usual delustered yarns, the yarns prepared in accordance with our invention retain their original dull or delustered appearance. In addition, we have found that organic derivative of cellulose yarns containing polymers of ethylene oxide have a considerably increased affinity for dyestuffs normally employed for dyeing organic derivative of cellulose materials and may be dyed in deeper shades by such dyestufis with less processing than yarns having a basis of an organic derivative of cellulose as heretofore prepared. This increased dyeing afiinity is not only achieved in yarns which have been delustered but, as stated, yarns in which the ethylene oxide polymer is still present likewise exhibit this desirable property. Moreover, films or foils may be formed from solutions containing polymers of ethylene oxide, which films or foils, upon being given a delustering treatment, are permanently delustered.
The polymers of ethylene oxide employed in accordance with our invention may be prepared in any suitable manner as by contactin liquid ethylene oxide at suitable temperatures with fullers 'earth or other similar material containing aluminum oxide. The products of polymerization are mixed polymers and may range from a syrupy liquid through waxy solids to rubbery compounds; By suitable treatment the polymers may be separated into several, fractions. Each of the several fractions contains polymers of different degrees of polymerization but of substantially similar or related characteristics.
- However, each fraction co tains polymers having degrees of polymerization different from those of the other fraction. While the heterogeneous mixture of polymers may be employed in our process prior to being separated into individual components, we preferably separate the mixture into its fractions and employ those fractions which are entirely water-soluble and fully compatible with the organic derivatives of cellulose employed. I
The ethylene oxide polymers may be added in varying amounts to the solutions from which the yarns, filaments, films, foils or other plastic materials, and the like, may be prepared. We have found that excellent results may be achieved when from 1 to 50%, and preferably from 5 to 10%, of ethylene oxide .polymers, based on the weight of the organic derivative of cellulose contained therein, is added to the solutions from which the filaments, films, etc. are prepared. The solutions containing the ethylene oxide polymers, after thorough mixing to obtain uniformity, may,be filtered and then extruded through the orifices of a spinneret either into an evaporative atmosphere as in dry spinning or into a coagulative medium as in wet spinning. Such solutions of the organic derivatives of cellulose material ranging in thickness the like, and the solvent evaporated therefrom.
Filaments spun from solutions containing the ethylene oxide polymers may be the fine filaments having a denier of, say, 1 to 10, such as are used for making yarns, or they may be much heavie i. e. having adenier of, say, 50 to 2.000, which may be used for artificial bristles or, when flattened, may be used for artificial straw. Our invention may also be advantageously employed for making films, foils and other products where strength and delusterability are important. The solution of organic derivative of cellulose containing the polymers may from that of thin foil, to that of film and of sheets of substantial thickness.
The delustering treatment is preferably carried out in hot aqueous media. We have found that water at elevated temperature makes an excellent delustering agent. Wet steam may also be employed. In some instances, the aqueous delustering bath may also contain other substances such as soap. salts, acid salts, pine oil, tetralin, etc. which accelerate or enhance the delustering action of the bath. While we preferably employ these solutions at or near the boiling point, i. e. about 100 C., temperatures as low as 60 C. may be advantageously employed.
Since at least a substantial proportion of the be cast or extruded to form sheet Example I To a solution of 1 part by weight of cellulose acetate in 3 parts by weight of acetone there is ethylene oxide polymers employed are watersoluble, the action of the delustering bath, i. e. the aqueous medium, causes the polymers contained in the materials being treated to dissolve out of the same to a substantial degree. The time necessary for the removal of the water-soluble ethylene oxide polymers from the materials being treated varies greatly and depends in the main upon the extent to which it is desired to remove them and the relative thickness of the filaments, yarn, foil, film or other material being delustered.
.When employing water at a temperature of about 100 C. for the delustering bath, a satisfactory degree of delustering may be obtained by maintaining the materials being treated in the bath for from 30 to 120 minutes. By treating the materials containing ethylene oxide polymers in this way, a completely delustered and substantially opaque product may be obtained.
While our invention is particularly applicable for the preparation of permanently delustered filaments, yarns, foils, films and other products having a basis of cellulose acetate, other organic derivatives of cellulose, such as other organic esters and ethers of cellulose, may be employed. Examples of such other organic esters of cellulose are cellulose propionate and cellulose butyrate andmixed esters such as cellulose acetate-propionate and cellulose acetate-butyrate, while examples of cellulose ethers are ethyl cellulose and benzyl cellulose.
In preparing the solution of the organic derivatives of cellulose containing the ethylene oxide, polymers any suitable solvent in which both the organic derivatives of cellulose and the ethylene oxide polymers are soluble may be employed.
Examples of such solvents are acetone, acetone and ethyl or methyl alcohol, chloroform, ethylene dichloride, ethylene dichloride and ethyl or By this treatment the yarn The depth of shade are considerably greater than that methyl alcohol, methylene chloride and ethyl or methyl alcohol, and ethylene formal.
In order further to illustrate our invention, but without being limited thereto, the following examples are given:
added 5% on the weight of the cellulose acetate 50 C. and having a molecular weight of about 4,000. The resulting solution is thoroughly mixed and filtered and is then processed, employing a dry-spinning method, into a yarn of 124 denier having 60 filaments. The yarn thus prepared is backwound on to a stainless steel bobbin and the bobbin holding the yarn is then immersed in boiling water for 15 minutes and is then dried. The yarn produced is completely and permanently delustered and has a tenacity of 1.32 grams per denier. Pigmented yarn of the same denier and having the same number of filaments h a tenacity of only 1.05.
Example I] A film .0026 inch in thickness is poured or cast from the solution prepared as indicated in Exampie 1. This film is found to have a breaking strength of 5,700 pounds per square inch, an elongation of 6% and is transparent. After being treated in boiling water for 15 minutes the ethylene oxide polymer contained therein is removed, the film becoming completely opaque. The strength of the resulting opaque film, i. e. the breaking strength, is found to have risen to 6,700 lbs. per square inch and the elongation to 14.2%.
Emmzlle III Yarn prepared in the manner indicated in Example I and still containing the ethylene oxide polymer therein is delustered by treatment for one hour at 98-100 C. in a bath containing 20 grams per liter of sodium oleate. The delustered yarn is then dyed for 30 minutes at C. in a bath containing 1% of lzl-dimethyl-aminoanthraquinone based on the weight of the yarn, 0.25 gram per liter of sodium oleate soap and 3 cos. per liter of Celascour (a mixture of Turkey red oil, xylene and water). The yarn is then rinsed well in water at 65 and then in cold water. is delustered and dyed a blue shade, the degree of delustering and depth of shade being greater than that produced on cellulose acetate yarn which is free from ethylene oxide polymer.
Where the above blue dyestuif is replaced by Celliton Blue AF or by Setacyl Direct Discharge Blue G equally satisfactory results are obtained.
Example IV Yarn prepared in the manner indicated in Example I, and while still containing the ethylene oxide polymer in the yarn structure, is treated in a bath comprising 1% of 1:4-dimethyl-aminoanthraquinone based on the weight of the yarn to be dyed, 0.25 gram per liter of sodium oleate soap and 3.0 ccs. per liter of Celascour. The yarn is immersed in the bath maintained at 98-100 C. for one hour. The yarn is simultaneously delustered and dyed a blue shade by this treatment. and degree of delustering achieved when cellulose acetate yarn not containing the ethylene oxide polymer is given a like treatment in the bath.
Example V To a solution of 1 part by weight of cellulose acetate in 3 parts by weight of acetone is added 10% on the weight of cellulose acetate of ethylene oxide polymer melting at about 50 C. and having a molecular weight of about 4,000. The solution is mixed and filtered and is then dry spun into a yarn of 180 denier having 40 filaments. The resulting yarn is then given a crepe twist of 70 turns per inch during an up-twisting operation whilebeing subjected to the action of steam during the actual insertion of the twist. This crepe yarn is employed for weaving a crepe fabric having 74 picks per inch on a warp of 120 ends of a 100 denier, 40 filament cellulose acetate yarn of turns per inch. The original width of this fabric is 45 inches. When this fabric is given a boil-off at 98 C. in an aqueous boil-off bath to develop the crepe, the boil-ofl width decreases to 37 inches after treatment for 60 minutes. The resulting fabric presents a pronounced and pleasing crepe effect. I
It is to be understood that the foregoing detailed description is merely given by way of illustration and that many variations may be made therein without departing from the spirit of our invention.
Having described our invention, what we desire to secure by Letters Patent is:
1. In a process for the production of permathroughout the mass thereof a polymerized ethylene oxide having a consistency from a syrupy liquid to a solid in an amount equal to from 1 to based on the weight of the organic substitution derivative of cellulose present in said filamentary materials, weaving said crape twisted filamentary materials into a fabric, and then subjecting said fabric to the action of a hot aqueous medium so as to cause said fabric to exhibit a crepe effect and a permanent deluster.
2. In a process for the production of permanently delustered crepe fabrics, the steps of applying a crepe twist to filamentary materials having a basis of cellulose acetate and having uniformly incorporated throughout the mass thereof a polymerized ethylene oxide having a consistency from a syrupy liquid to a solid in an amount equal to from 1 to 50% based on the weight of the cellulose acetate present in said filamentary materials, weaving said crepe twisted filamentary materials into a fabric, and then subjecting said fabric to the action of a hot aqueous medium so as to cause said fabric to exhibit a crepe effect and a permanent deluster.
3. In a process for the production of permanently delustered crepe fabrics, the steps of applying a crepe twist to filamentary materials having a basis of cellulose acetate and having uniformly incorporated throughout the mass thereof a polymerized ethylene oxide having a consistency from a syrupy liquid to a solid in an amount equal to from 5 to 10% based on the weight of the cellulose acetate present in said filamentary materials, weaving said crepe twisted filamentary materials into a fabric, and then subjecting said fabric to the action of a hot aqueous medium so as to cause said fabric to exhibit a crepe effect and a permanent deluster.
RICHARD R. SITZLER.
JOSEPH E. BLUDWORTH.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US406187A US2394212A (en) | 1941-08-09 | 1941-08-09 | Manufacture of artificial products |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US406187A US2394212A (en) | 1941-08-09 | 1941-08-09 | Manufacture of artificial products |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2394212A true US2394212A (en) | 1946-02-05 |
Family
ID=23606899
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US406187A Expired - Lifetime US2394212A (en) | 1941-08-09 | 1941-08-09 | Manufacture of artificial products |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2394212A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2990604A (en) * | 1956-07-18 | 1961-07-04 | Ici Ltd | Process of thermally treating and lubricating polyethylene terephthalate filaments and yarns |
-
1941
- 1941-08-09 US US406187A patent/US2394212A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2990604A (en) * | 1956-07-18 | 1961-07-04 | Ici Ltd | Process of thermally treating and lubricating polyethylene terephthalate filaments and yarns |
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