US2255766A - Treatment of artificial textile - Google Patents
Treatment of artificial textile Download PDFInfo
- Publication number
- US2255766A US2255766A US2255766DA US2255766A US 2255766 A US2255766 A US 2255766A US 2255766D A US2255766D A US 2255766DA US 2255766 A US2255766 A US 2255766A
- Authority
- US
- United States
- Prior art keywords
- materials
- ability
- subjected
- stretching
- absorb moisture
- 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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- 239000004753 textile Substances 0.000 title description 5
- 238000011282 treatment Methods 0.000 title description 5
- 239000000463 material Substances 0.000 description 28
- 238000000034 method Methods 0.000 description 13
- 239000004014 plasticizer Substances 0.000 description 13
- 229920002678 cellulose Polymers 0.000 description 8
- 239000001913 cellulose Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000008961 swelling Effects 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- PCYQQSKDZQTOQG-NXEZZACHSA-N dibutyl (2r,3r)-2,3-dihydroxybutanedioate Chemical compound CCCCOC(=O)[C@H](O)[C@@H](O)C(=O)OCCCC PCYQQSKDZQTOQG-NXEZZACHSA-N 0.000 description 4
- 238000010348 incorporation Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 229920002301 cellulose acetate Polymers 0.000 description 3
- LMYRWZFENFIFIT-UHFFFAOYSA-N toluene-4-sulfonamide Chemical compound CC1=CC=C(S(N)(=O)=O)C=C1 LMYRWZFENFIFIT-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000012237 artificial material Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000009940 knitting Methods 0.000 description 2
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 2
- 229940124530 sulfonamide Drugs 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 238000009941 weaving Methods 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- UWNXGZKSIKQKAH-UHFFFAOYSA-N Cc1cc(CNC(CO)C(O)=O)c(OCc2cccc(c2)C#N)cc1OCc1cccc(c1C)-c1ccc2OCCOc2c1 Chemical compound Cc1cc(CNC(CO)C(O)=O)c(OCc2cccc(c2)C#N)cc1OCc1cccc(c1C)-c1ccc2OCCOc2c1 UWNXGZKSIKQKAH-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000004348 Glyceryl diacetate Substances 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- HSUIVCLOAAJSRE-UHFFFAOYSA-N bis(2-methoxyethyl) benzene-1,2-dicarboxylate Chemical compound COCCOC(=O)C1=CC=CC=C1C(=O)OCCOC HSUIVCLOAAJSRE-UHFFFAOYSA-N 0.000 description 1
- 238000000578 dry spinning Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 235000019443 glyceryl diacetate Nutrition 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 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
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/438—Sulfonamides ; Sulfamic acids
Definitions
- This invention relates to improvements in the manufacture of artificial materials, and particularly to improvements in the manufacture of artificial filaments, yarns and similar materials having a basis of cellulose acetate or other organic derivative of cellulose.
- Certain operations to which textile materials of organic derivatives of cellulose may be subjected during or subsequent to their formation may yield products having a smaller ability to absorb moisture than the materials obtained directly by the normal dry spinning process and in consequence the normal methods of achieving the best results in knitting, weaving and other operations are either not applicable at all or give less satisfactory results than with ordinary textile materials.
- Such operations are processes in which artificial filaments and, the like are stretched in the presence of hot water or steam or, during or subsequent to their production, in solutions of swelling agents or organic solvents to increase their tenacity, and processes in which they are esterified.
- the properties, and particularly the flexibility, of artificial filaments, yarns and similar materials made of organic derivatives of cellulose which have been subjected to such operations, for example the stretching and esteriflcation processes referred to above, may be improved by incorporating suitable plasticisers in the materials.
- the incorporation is effected after the completion of the operation, though it may, if desired, be effected before such treatment when the latter is an after-treatment or even prior to the formation of the materials by incorporating the plasticisers in the spinning solution from which the materials are produced.
- plasticisers which may be employed in accordance with the process of the present invention are para-toluene sulphonamide and para-toluene methyl sulphonamide, tributyl phosphate, dibutyl phthalate, dimethyl glycol phthalate, diethyl glycol phthalate, .dibutyl tartrate and diacetin.
- plasticisers which are hydrophile or even soluble in water to a slight extent are employed.
- An improvement in the flexibility of the materials may be effected by the incorporation of a comparatively small proportion of plasticiser, for example from I to 2 up to 5% of the weight of the materials, and preferably the amount incorporated is of this order. Higher proportions, for example 1001' 20% or even more, may be incorporated if desired, but too high a proportion of plasticiser may tend to make the materials plastic so that they are easily deformed by even slight tension or pressure.
- Incorporation of the plasticiser in the materials may be eifected by treating the materials with a liquid medium containing the plasticiser in the form of a. solution or of an emulsionor suspension in a suitable liquid medium which does not dissolve the base of the artificial materials or swell it to too great an extent. A certain amount of swelling may be of value in assisting the incorporation.
- suitable liquids are water, alcohol, benzene, toluene, ethyl acetate, diethyl ether, di-isopropyl ether, ligroin and cyclohexane.
- Solutions of suitable substances may also be employed, for example solutions of methylene or ethylene dichloride in benzene or carbon tetrachloride, aqueous solutions of acetene, methylene ethylene etherand other solvents for the organic derivatives of cellulose,
- Example 1 A cellulose acetate yarn which has been stretched in wet steam according to the process described in U. S. application 8. No. 48,084 filed 4th November 1935, is immersed in bank form in a 2% aqueous emulsion of dibutyl tartrate containing a small proportion of the emulsifying agent sold under the registered trademark Igepon. Th emulsion is maintained at about C. When sufllcient dibutyl tartrate has been absorbed by the yarn the latter is withdrawn from the treating liquid, and dried.
- j yarns and I an organic derivative of cellulose have their 1 ability to absorb moisture reduced by stretching forming operation.
- plasticisers which 1 are preferably hydrophile, may be substituted for the dibutyl tartrate and p-toluene-sulphonamide specified in the examples.
- the step of restoring the ability to absorb moisture which comprises incorporating a hydrophile or slightly water-soluble plasticizer in the materials after they have been subjected to the stretching operation but before they are subjected to a fabric-forming operation.
- the step of restoring the ability to absorb moisture which comprises incorporating a sulphonamide in the materials in a proportion up to 5% ofthe weight of the materials after they have been subjected to the stretching operation but before they are subjected to a fabric-forming operation.
- the step of restoring the ability to absorb moisture which comprises incorporating a sulphonamide in the materials in a proportion up to 5% of the weight of the materials after they have been subjected to the stretching operation but before they are subjected to a fabricforming' operation.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Artificial Filaments (AREA)
Description
Patented Sept. 16,1941
TREATMENT OF ARTIFICIAL TEXTILE MATERIALS Henry Dreyfus, London, England No Drawing. Application September 29, 1938, Se-
rial No. 232,353. 1937 This invention relates to improvements in the manufacture of artificial materials, and particularly to improvements in the manufacture of artificial filaments, yarns and similar materials having a basis of cellulose acetate or other organic derivative of cellulose.
In knitting, weaving and other textile operations it is well known that humidity either in the atmosphere or associated with the materials is of importance since it plays a very considerable part .a determining the flexibility of the materials undergoing these mechanical treatments and a proper adjustment of the humidity is essential to the production of good results.
Certain operations to which textile materials of organic derivatives of cellulose may be subjected during or subsequent to their formation may yield products having a smaller ability to absorb moisture than the materials obtained directly by the normal dry spinning process and in consequence the normal methods of achieving the best results in knitting, weaving and other operations are either not applicable at all or give less satisfactory results than with ordinary textile materials. Among such operations are processes in which artificial filaments and, the like are stretched in the presence of hot water or steam or, during or subsequent to their production, in solutions of swelling agents or organic solvents to increase their tenacity, and processes in which they are esterified.
I have now found that the properties, and particularly the flexibility, of artificial filaments, yarns and similar materials made of organic derivatives of cellulose which have been subjected to such operations, for example the stretching and esteriflcation processes referred to above, may be improved by incorporating suitable plasticisers in the materials. Preferably, the incorporation is effected after the completion of the operation, though it may, if desired, be effected before such treatment when the latter is an after-treatment or even prior to the formation of the materials by incorporating the plasticisers in the spinning solution from which the materials are produced.
Examples of plasticisers which may be employed in accordance with the process of the present invention are para-toluene sulphonamide and para-toluene methyl sulphonamide, tributyl phosphate, dibutyl phthalate, dimethyl glycol phthalate, diethyl glycol phthalate, .dibutyl tartrate and diacetin. Preferably, plasticisers which are hydrophile or even soluble in water to a slight extent are employed.
In Great Britain October 26, 5 Claims. (01. 8-129) An improvement in the flexibility of the materials may be effected by the incorporation of a comparatively small proportion of plasticiser, for example from I to 2 up to 5% of the weight of the materials, and preferably the amount incorporated is of this order. Higher proportions, for example 1001' 20% or even more, may be incorporated if desired, but too high a proportion of plasticiser may tend to make the materials plastic so that they are easily deformed by even slight tension or pressure.
Incorporation of the plasticiser in the materials may be eifected by treating the materials with a liquid medium containing the plasticiser in the form of a. solution or of an emulsionor suspension in a suitable liquid medium which does not dissolve the base of the artificial materials or swell it to too great an extent. A certain amount of swelling may be of value in assisting the incorporation. Examples of suitable liquids are water, alcohol, benzene, toluene, ethyl acetate, diethyl ether, di-isopropyl ether, ligroin and cyclohexane. Solutions of suitable substances may also be employed, for example solutions of methylene or ethylene dichloride in benzene or carbon tetrachloride, aqueous solutions of acetene, methylene ethylene etherand other solvents for the organic derivatives of cellulose,
Example 1 A cellulose acetate yarn which has been stretched in wet steam according to the process described in U. S. application 8. No. 48,084 filed 4th November 1935, is immersed in bank form in a 2% aqueous emulsion of dibutyl tartrate containing a small proportion of the emulsifying agent sold under the registered trademark Igepon. Th emulsion is maintained at about C. When sufllcient dibutyl tartrate has been absorbed by the yarn the latter is withdrawn from the treating liquid, and dried.
j yarns and I an organic derivative of cellulose have their 1 ability to absorb moisture reduced by stretching forming operation.
ther acetylated with acetic anhydride in the presence of ferric chloride and hydrochloric acid according to the process described in U. S. ap-
a bath of 4 parts of p-toluene-sulphonamide in 100 parts of 3% aqueous ammonia until suflicient plasticiser has been taken up. The hanks are then withdrawn and dried.
' Similar proportions of other plasticisers, which 1 are preferably hydrophile, may be substituted for the dibutyl tartrate and p-toluene-sulphonamide specified in the examples.
Having described my invention, what I desire to secure by Letters Patent is:
1. In processes wherein artificial filaments, ar materials having a basis of in the presence of hot water, steam or organic solvents or swelling agents, the step of restoring the ability to absorb moisture which comprises incorporating a plasticizer in the materials after they have been subjected to the stretching operation but before they are subjected to a fabric- 2. In processes wherein artificial filaments, yarns and similar materials having a basis of an organic derivative of cellulose have their ability to absorb moisture reduced by stretching-in the presence of hot water, steam or organic solvents or swelling agents and are esterified, the step of restoring the ability to absorb moisture which comprises incorporating a plasticizer in the materials after the stretching and esterifying op- I plication S. No. 39,290 filed 5th September 1935, Patent No. 2,159,012, is soaked in hank form in erations-but before they are subjected to a fabric-forming operation.
3. In processes wherein artificial filaments, yarns and similar materials having a basis of cellulose actate have their ability to absorb moisture reduced by stretching in the presence of hot water, steam or organic solvents or swelling agents, the step of restoring the ability to absorb moisture which comprises incorporating a hydrophile or slightly water-soluble plasticizer in the materials after they have been subjected to the stretching operation but before they are subjected to a fabric-forming operation.
4. In processes wherein artificial filaments, yarns and similar materials having a basis of an organic derivative of cellulose have their ability to absorb moisture reduced by stretching in the presence of hot water, steam or organic solvents or swelling agents, the step of restoring the ability to absorb moisture which comprises incorporating a sulphonamide in the materials in a proportion up to 5% ofthe weight of the materials after they have been subjected to the stretching operation but before they are subjected to a fabric-forming operation.
5. In processes wherein artificial filaments, yarns and similar materials having a basis of cellulose acetate have their ability to absorb moisture reduced by stretching in the presence of hot water, steam or organic solvents or swelling agents, the step of restoring the ability to absorb moisture which comprises incorporating a sulphonamide in the materials in a proportion up to 5% of the weight of the materials after they have been subjected to the stretching operation but before they are subjected to a fabricforming' operation.
' HENRY DREYFUS.
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2255766A true US2255766A (en) | 1941-09-16 |
Family
ID=3432162
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US2255766D Expired - Lifetime US2255766A (en) | Treatment of artificial textile |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2255766A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3012396A (en) * | 1955-07-05 | 1961-12-12 | Celanese Corp | Process for producing voluminous yarn |
-
0
- US US2255766D patent/US2255766A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3012396A (en) * | 1955-07-05 | 1961-12-12 | Celanese Corp | Process for producing voluminous yarn |
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