US2045347A - Production of threads and the like - Google Patents
Production of threads and the like Download PDFInfo
- Publication number
- US2045347A US2045347A US638177A US63817732A US2045347A US 2045347 A US2045347 A US 2045347A US 638177 A US638177 A US 638177A US 63817732 A US63817732 A US 63817732A US 2045347 A US2045347 A US 2045347A
- Authority
- US
- United States
- Prior art keywords
- cellulose
- ester
- acetone
- filaments
- spinning
- 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
- 238000004519 manufacturing process Methods 0.000 title description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 44
- 229920002678 cellulose Polymers 0.000 description 33
- 239000001913 cellulose Substances 0.000 description 24
- 229920002301 cellulose acetate Polymers 0.000 description 19
- 238000009987 spinning Methods 0.000 description 19
- 238000000034 method Methods 0.000 description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
- 150000002148 esters Chemical class 0.000 description 15
- 235000019441 ethanol Nutrition 0.000 description 13
- 239000011877 solvent mixture Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 9
- 239000010902 straw Substances 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 7
- 150000002895 organic esters Chemical class 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Natural products CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 238000000578 dry spinning Methods 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 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
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 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 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000005909 ethyl alcohol group Chemical group 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- RGHXWDVNBYKJQH-UHFFFAOYSA-N nitroacetic acid Chemical class OC(=O)C[N+]([O-])=O RGHXWDVNBYKJQH-UHFFFAOYSA-N 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- -1 ribbons Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000002166 wet spinning Methods 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
- 356,170 processes are dewith relatively small quantities of water, this phescribed for the manufacture of filaments and nomenon may detract somewhat from the comother spun products from solutions of cellulose flareal valueof the products.
- esters of low degree of esterification i. e. esters
- the above spinning solutions may be spun by having less than two ester groups per cellulose dry or wet spinning methods.
- the said patent refers to disditions will, of course, be adjusted in accordance 10 solving the saidestersin mixtures of acetone with with the nature of the product desired. 7 For Wate'r forthe purpose of manufacturing the spun example the spinning conditions may be adjustproducts.
- filaments of round cross-section sults may be obtained by employing as solvent or of'relatively flat cross-section, or they may be for esters of low ester content, e. g. those deadjusted toobtain hollow or voluminous filaments, 15
- the temperatures necessary to obtain a particular realcohol may, for example, constitute as much as sult, employing as solvent mixture the mixture diacetates or cellulose acetates of slightly lower somewhat higher than those which may be used acetyl content. Usually good results are obtainto obtain similar products using acetone or mixable with proportions of -40% of alcohol and tures-of acetone with small quantities of water. 70-60% of acetone.” With an acetate of 52% Filaments prepared from the spinning solutions 30 acetyl content, somewhat less alcohol may be used. described herein may be stretched'in any suitable 30 The alcohol in the above mixtures may be partly manner, or maybe -shrunk, if desired, by any replaced by water.
- Such filaments may-also be acetate having an acetyl value of about 48% a submitted to partial or total saponifieation, or solvent mixture may comprise 60-75% of acetone treated by processes calculated to modify their 20-35% of methyl or ethyl alcohol and -5-10% of dyeing l properties. Processes according to the water. Instead of acetone other ketones may be present invention may also be used in conjunction used as for example methyl ethyl ketone. with processes for reducing or modifying the Cellulose esters of relatively low ester content lustre of the filaments. for use in this invention may be prepared by any The following example will serve to illustrate 40 suitable process.
- 356,170 also attained in the process acsolved to form a 25% solution in a solvent mixcording to the present invention but in addition, ture consisting of 70 parts of acetone, 25 parts inasmuch as it is possible to replace far more aceof ethyl alcohol and 5 parts of water.
- the solu- 50 tone by alcohol or by mixtures of alcohol and tion so obtained is extruded from suitable orifices water than is possible in the case of water only, into a heated evaporative medium such as air or considerable economies can be effected. Moreother gas maintained for example at a temperaover, I find that when spinning at high speed, ture of 7585 C. and the filaments thus formed for example 200-300 metres per minute or more, are associated by twisting.
- the invention is particularly important in re- 55 lation to the spinning of filaments and like products from cellulose acetates, but may also be employed for the production of filaments and other products from cellulose propionates, cellulose butyrates, cellulose formates, cellulose nitroacetates and like organic esters of cellulose and mixed ether-esters of cellulose such as ethyl cellulose acetate and oxyethyl cellulose acetate.
- the step oi forming said solution by dissolving said organic 'ester of cellulose in a solvent mixture containing a substance selected from the group consisting of acetone and methyl ethyl ketone, and an alcohol.
- a spinning solution for the production of filaments, yarns, bristles, straw, ribbons, films and the like comprising an organic ester of cellulose of relatively low ester content ,dissolved in a solvent medium containing acetone and a lower fatty alcohol, said ester being the only cellulose esterpresent in the solution.
- a spinning solution for the production of filaments, yarns, bristles, straw, ribbons and the like, which comprises a cellulose acetate contain: ing less than two acetyl radicles per molecule of cellulose, considered as Cal-1100s, dissolved in a solvent mixture comprising acetone and ethyl alcohol, said cellulose acetate being the onlycellulose ester present in the solution.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Artificial Filaments (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB30369/31A GB391783A (en) | 1931-11-02 | 1931-11-02 | Improvements in the production of threads, films and the like |
Publications (1)
Publication Number | Publication Date |
---|---|
US2045347A true US2045347A (en) | 1936-06-23 |
Family
ID=10306572
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US638177A Expired - Lifetime US2045347A (en) | 1931-11-02 | 1932-10-17 | Production of threads and the like |
Country Status (3)
Country | Link |
---|---|
US (1) | US2045347A (xx) |
FR (1) | FR743625A (xx) |
GB (1) | GB391783A (xx) |
-
0
- FR FR743625D patent/FR743625A/fr not_active Expired
-
1931
- 1931-11-02 GB GB30369/31A patent/GB391783A/en not_active Expired
-
1932
- 1932-10-17 US US638177A patent/US2045347A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
FR743625A (xx) | 1933-04-03 |
GB391783A (en) | 1933-05-02 |
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