US1800944A - Process for improving vegetable textile material - Google Patents
Process for improving vegetable textile material Download PDFInfo
- Publication number
- US1800944A US1800944A US31446A US3144625A US1800944A US 1800944 A US1800944 A US 1800944A US 31446 A US31446 A US 31446A US 3144625 A US3144625 A US 3144625A US 1800944 A US1800944 A US 1800944A
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- United States
- Prior art keywords
- solution
- alkali
- textile material
- alkali solution
- ester
- 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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- 239000000463 material Substances 0.000 title description 98
- 238000000034 method Methods 0.000 title description 74
- 239000004753 textile Substances 0.000 title description 53
- 235000013311 vegetables Nutrition 0.000 title description 48
- 239000000243 solution Substances 0.000 description 94
- 239000003513 alkali Substances 0.000 description 81
- 150000002485 inorganic esters Chemical class 0.000 description 37
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 31
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 30
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 23
- 229910021653 sulphate ion Inorganic materials 0.000 description 23
- 150000002148 esters Chemical class 0.000 description 15
- 239000002253 acid Substances 0.000 description 14
- -1 aralkyl halide Chemical class 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 11
- 239000004744 fabric Substances 0.000 description 11
- 235000011121 sodium hydroxide Nutrition 0.000 description 10
- 238000005406 washing Methods 0.000 description 10
- 150000003839 salts Chemical class 0.000 description 9
- 239000002562 thickening agent Substances 0.000 description 9
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 8
- 229920000742 Cotton Polymers 0.000 description 8
- 150000001350 alkyl halides Chemical class 0.000 description 8
- 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 8
- 230000001376 precipitating effect Effects 0.000 description 8
- 229920002678 cellulose Polymers 0.000 description 7
- 239000001913 cellulose Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 230000005484 gravity Effects 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000001117 sulphuric acid Substances 0.000 description 5
- 235000011149 sulphuric acid Nutrition 0.000 description 5
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 244000025254 Cannabis sativa Species 0.000 description 2
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 2
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- 240000000491 Corchorus aestuans Species 0.000 description 2
- 235000011777 Corchorus aestuans Nutrition 0.000 description 2
- 235000010862 Corchorus capsularis Nutrition 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- 239000004375 Dextrin Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241000208202 Linaceae Species 0.000 description 2
- 235000004431 Linum usitatissimum Nutrition 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 2
- 235000009120 camo Nutrition 0.000 description 2
- 235000005607 chanvre indien Nutrition 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 235000019425 dextrin Nutrition 0.000 description 2
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000011487 hemp Substances 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
- 238000005517 mercerization Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- ALWXETURCOIGIZ-UHFFFAOYSA-N 1-nitropropylbenzene Chemical compound CCC([N+]([O-])=O)C1=CC=CC=C1 ALWXETURCOIGIZ-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 240000008564 Boehmeria nivea Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241001397173 Kali <angiosperm> Species 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- 239000001063 aluminium ammonium sulphate Substances 0.000 description 1
- 235000011124 aluminium ammonium sulphate Nutrition 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000001164 aluminium sulphate Substances 0.000 description 1
- 235000011128 aluminium sulphate Nutrition 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 1
- 229940073608 benzyl chloride Drugs 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229960004643 cupric oxide Drugs 0.000 description 1
- JJCFRYNCJDLXIK-UHFFFAOYSA-N cyproheptadine Chemical compound C1CN(C)CCC1=C1C2=CC=CC=C2C=CC2=CC=CC=C21 JJCFRYNCJDLXIK-UHFFFAOYSA-N 0.000 description 1
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000008098 formaldehyde solution Substances 0.000 description 1
- 229920000591 gum Polymers 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000009896 oxidative bleaching Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000009895 reductive bleaching Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
Classifications
-
- 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
- D06M13/08—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with halogenated hydrocarbons
-
- 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
- D06M13/244—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 sulfur or phosphorus
- D06M13/248—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 sulfur or phosphorus with compounds containing sulfur
- D06M13/256—Sulfonated compounds esters thereof, e.g. sultones
Definitions
- the invention consists in treating with an inorganic ester of a mono-hydric alcohol, for V instance, a dialkyl sulphate, an alkyl halide or an aralkyl halide, in presence of alkali, I spun or woven material consisting of or containing a vegetable fibre, particularly cotton.
- a mono-hydric alcohol for V instance, a dialkyl sulphate, an alkyl halide or an aralkyl halide
- the process may be conducted at room temperature.
- binding or thickening agent such as starch, dextrin, British gum, albumen or the like.
- the ester or a solution or suspension thereof may be rolled into the material. Any other method may, however, be employed, such as spraying. In order that the distribution of the ester throughout the textile material may be as uniform as possible, the material may, if desired, be passed through one or more pairs of rollers during the treatment, or may be subjected to pressure by other means.
- Any of the subsidiary operations usual in mercerization or proposed for this purpose may also be used in the present invention, for examplelustering, pressure, mechanical beating, and the like.
- the material may also be stretched only during the action of the alkali solution or of the inorganic ester, or it may be stretched after the impregnation with the alkali solution, and may remain stretched during the actionof the ester, during the.
- the alkali solution mixed with a suitable thickening agent (such as starch, denatured albumen, a cellulose-hydrate which is soluble in alkali, an alkylor oxyalkyl-cellulose derivative which is soluble in alkai or in water, or a cellulose-hydroxyparaflinmonocarboxylic acid or the like), is printed in any desired pattern on the woven material, which is then treated with an inorganic ester of a monohydric alcohol, advantageously with a dialkyl sulphate, an alkyl halide or an aralkyl halide as already described.
- a suitable thickening agent such as starch, denatured albumen, a cellulose-hydrate which is soluble in alkali, an alkylor oxyalkyl-cellulose derivative which is soluble in alkai or in water, or a cellulose-hydroxyparaflinmonocarboxylic acid or the like
- the material is treated with the inorganic ester as in the first method of carrying out the invention, and is then treated with an acid or salt, and dried. This method yields strongly lustrous efl'ects on a less lustrous background, or vice versa.
- the material After the material has been in contact with the inorganic ester for a short period (for example 10 minutes), or for a longer period (for example 12 hours), it is washed and dried or introduced into a dilute solution (for example of 10-20 per cent. strength) of sulphuric or acetic acid, or into a solution ofammonium chloride or ammonium sulphate of 20-30-per cent.
- a dilute solution for example of 10-20 per cent. strength
- sulphuric or acetic acid or into a solution ofammonium chloride or ammonium sulphate of 20-30-per cent.
- Bleached or unbleached cotton fabric or yarn is impregnated with a solution of 10 per cent. strength of di-methyl sulphate, di-ethyl sulphate, ethyl iodide, methyl iodide or ethyl bromide in alcohol or benzol
- the fabric may be stretched ples 1 (a) to 1 (c), with the exceptionthat' during or after the treatment with the al- ;kali solution. A silky lustre is produced.
- the treatment with sulphuric acid may also precede mercerization of the fabric, for
- precipitating agent means acids, salts, acid salts, m xtures of acids and salts, in short all precipitatin agents known in the viscose industry as we as organic acids or aqueous solutions there of, alcohols, tannic acids, and. formaldehyde.
- a process for improving vegetable textile material which comprises treating it with an alkali solution and thereafter acting on it with an inorganic ester of a monohydric alcohol in presence of at least a portion of the alkali solution used in the treatment.
- a process for improving vegetable textile material which comprises treating it with a solution of an alkali and thereafter reacting on at least one side with an inorganic ester of a monohydric alcohol mixed with a thickening agent.
- a process for improving vegetable textile material which comprises treating it with a solution of an alkali and printing it in the presence of alkali with an inorganic ester of a monohydric alcohol mixed with a thickening agent.
- a process for improving vegetable textile material which comprises acting on it at a raised temperature, in the presence of an alkali, with an inorganic ester of a monohydric alcohol.
- a process for improving vegetable textile material which comprises acting on it in presence of an alkali with an inorganic ester of a monohydric alcohol, thereafter treating it with a precipitating agent and washing it.
- a process for improving vegetable textile material which comprises acting on it in'presence of an alkali with an inorganic ester of a monohydric alcohol and stretching the material during at least a portion of the process.
- a process for improvingvegetable textile material which comprises treating it with an alkali solution, thereafter reacting on it with an inorganic ester of a monohydric alcohol, and stretching the material during at least a portion of the process.
- a process for improving vegetable textile material which comprises treating it with an alkali solution and after removing at least a portion of the water by drying, reacting on it with a dialkyl sulphate.
- a process for improving vegetable textile material which comprises treating it at certain parts with an alkali solution and thereafter reacting on it with a dialkyl sulphate.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Treatment Of Fiber Materials (AREA)
Description
Patented Apr. 14, 1931 PATENT OFFICE LEON LILIENIELD, OF VIENNA, AUSTRIA PROCESS FOR IMPBQVING VEGETABLE TEXTILE MATERIAL No Drawing. application filed llay 19, 1925, Serial No. 31,446, and in Austria Il jay 30, 1924.
This invention relates to a process for improving textile materials of vegetable origin. According to the invention very valuable properties are conferred upon woven and spun material of vegetable origin by treating them in presence of alkalies with an inorganic ester of a monohydric alcohol, for
instance a dialkyl-sulplrate, an alkyl halide or an aralkyl halide. This process imparts to the materials a silky gloss of great brilliance and a pleasing finish of elastic feel.
' The invention consists in treating with an inorganic ester of a mono-hydric alcohol, for V instance, a dialkyl sulphate, an alkyl halide or an aralkyl halide, in presence of alkali, I spun or woven material consisting of or containing a vegetable fibre, particularly cotton.
The material may be treated with the inorganic ester and.the alkali either simultaneously or in either sequence.
Among the alkalies which can be used, the most important are the caustic alkalies. Alkali metal sulphides may, however,'be used, although the results obtained are usually less satisfactory.
There may be treated according to the invention all vegetable fibres, such as linen, flax, hemp, ramie, jute, and especially cotton, in the form of pure vegetable (for example, pure 0 cotton) or mixed goods, in the form of yarn in skeins or cops, or in the form of warps.
The textile goods consisting of or containing the vegetable fibre may be treated ac- 3 cording to the invention either in the crude 5 state or after a preliminary treatment (for instance, boiling, or heating under pressure with sodium carbonate solution or dilute alkali solution or both), either moistened or unmoistened, with or 'without removing the -fatty constituents, either unbleached or after bleaching with an oxidizing or reducing bleaching agent, and with or without mer-' cerizing. The material may also be previously prepared in known manner by treatment with a hydrolyzing or gelatinizing agent (for example with a strong mineral acid such as sulphuric acid of 49-60 Baum specific gravity, phosphoric acid of -57v Baum specific gravity. hydrochloric acid of 24 Baum specific gravity, or nitric acid of 43-46" Baum specific gravity, or more, with an ammoniacal solution of cupric oxide, or with a cold or hot solution of calcium thiocyanate or other thiocyanate). The preliminary treatment may also consist in a combination of two or more of these processes.
The conditions under which the process is carriedout according to the invention may vary within Wide limits, and the invention is not limited to the illustrative examples of its practical application, which follow.
As examples, the following methods of carrying out the invention are given.
The first method consists in treating the woven or spun material first with a solution of an alkali and then acting on it with an inorganic ester of a monohydric alcohol, such as a dialkyl sulphate, an alkyl halide or an aralkyl halide. The textile material may be treated with the alkali solution in various ways; for example by dipping or soaking it in a small or large excess of the alkali solution; by dipping or soaking it in the alkali solution and removing the excess of alkali solution by squeezing, centrifuging or the like; by impregnating it in an impregnating mill, pgger or the like; by padding it between smooth or engraved rollers in a padding machine; by coating by means of closely engraved rollers in a rouleaux machine, advantageously with the addition of a thickening agent; by spraying, or by any other known method.
As alkali solution there may be used, for example, a solution of caustic soda oi: 10-50 per cent. strength; a solution of caustic soda of 12-40 er cent. strength has been found very suita le.
The quantity of alkali solution with wh ch the material is to be impregnated, or whlch is to be retained by the material, may be varied within wide limits. Thus, for instance, satisfactory results have been obtained when this quantity is from 2 to 10 times the weight of the textile material. As a rule, a quantity of from 2 to 4 times the weight of the material will be found to be suflicient.
The temperature of the alkali solution may also be chosen from a very wide range. Useful results are obtained at temperatures of strength .of the alkali solution.
from C. to +50 C. according to the Generally, if the alkali solution is not too weak, the process may be conducted at room temperature.
In order that the alkali solution may penetrate the fibres thoroughly, and increase the lustre, the woven or spun material may be caused topass between rollers during the treatment with the alkali solution, or it may otherwise be subjected to a high pressure. If desired the alkali solution may contain some alcohol.
The textile material which has been treated with alkali is then treated with an inorganic ester of a monohydric alcohol, for example with a dialkyl sulphate or an alkyl halide or an aralkyl halide, either immediately after the alkali treatment, or after standing (ripening? at room temperature or above for a short or ong period, and either in the wet state or after it has previously been partly or completely dried. The ester may be brought into contact with the material which has been treated with the alkali solution either as such, or dissolved in a suitable solvent, or suspended in an indifferent medium. There may be used as a solvent benzene, alcohol, a mixture of benzene and alcohol, or any other solvent. In order that the ester may be uniformly distributed throu bout the textile material, it
may be used, i desired, in admixture with a suitable binding or thickening agent, such as starch, dextrin, British gum, albumen or the like.
The ester may be added in various ways to the material which has been treated with the solution of alkali. The material may be impregnated or coated on one or both sides with the ester, or with a solution or emulsion thereof (in which case any excess may be removed, 1f deslred, by presslng or centrlfuging), or
the ester or a solution or suspension thereof may be rolled into the material. Any other method may, however, be employed, such as spraying. In order that the distribution of the ester throughout the textile material may be as uniform as possible, the material may, if desired, be passed through one or more pairs of rollers during the treatment, or may be subjected to pressure by other means.
For.introduci ng the ester there may be used any suitable apparatus known in the art of finishing or printing textiles.
The material which has been treated with the inorganic ester is then washed either directly, or soon after addition of the ester, or after it has been in contact with it for a short or long period (for example 2i hours) at room temperature or at a higher temperature (for example 50100 Q), and if deslred after previously having been dried, or it may advantageously be treated with a cold or warm solution of an inorganic or an organic acid, or of an acid salt, or of an f ammonium or other salt, or with a tannin ing operation.
solution or a formaldehyde solution, or with any other precipitating agent known in the viscose or ammoniacal-copper-oxide-cellulose industries, or with a mixture of such precipi tatin agents, and then washed and dried. It may e steamed before or after washing. 1
Any of the subsidiary operations usual in mercerization or proposed for this purpose may also be used in the present invention, for examplelustering, pressure, mechanical beating, and the like.
In order to produce a hi h grade, silky lustre, it is essential that the textile fibre should be stretched. It may be stretched throughout all the operations, that is, from,
the impregnation with the alkali solution at the commencement, to the washing and dry- The material may also be stretched only during the action of the alkali solution or of the inorganic ester, or it may be stretched after the impregnation with the alkali solution, and may remain stretched during the actionof the ester, during the.
treatment with the acid, salt, or the like, and
during the washing and optionally during The second method of carrying out the invention consists in reversing the order of the operations of the first method; that is to say, the textile material is first treated with the inorganic ester as such, or with a solution or a suspension thereof, and is then introduced into the alkali solution or impregnated, coated, or sprinkled, or sprayed therewith.
Since the inorganic esters have noaction on the fibre in absence of alkali, the treatment with alkali solution may follow the treatment with the inorganic ester at leisure. After the material has been brought into contact with the alkali solution, the inorganic ester is allowed to act for a certain time; this action may proceed at room temperature or at a higher temperature. In respect of the other conditions such as the quantitative proportions. the temperatures, the duration of the reaction, the stretching, and the finishing of the material, the conditions given in the first method of carrying out the process are equally applicable.
. By an appropriate selection of the work-' ing conditions. there may be obtained by the presentinvention silk-like effects which are ar superior to those which can be obtained by the usual methods of. memorization. In
lit
addition to the silky lustre, the woven or spun material possesses a finish which has a valuable, elastic feel. The silky lustre may be improved by one or more repetitions of the process.
The process according to the invention is also suitable for producing patterns, for which the following methods are of consequence:
1. Before the treatment with alkali solution, a pattern is printed or stencilled on the material by means of a reserve paste which prevents either mechanically or chemically the absorption of the alkali solution. Materials suitable for the reserve are, for instance, albumen, gums, acids (such as acetic acid, citric acid, tartaric acid, or an inorganic acid), alum, aluminium sulphate, ammonium sulphate, or other salts. The material is then treated with alkali solution and an inorganic ester of a monohydric alcohol, advantageously with a dialkyl sulphate, an alkyl halide or an aralkyl halide according to the method described. in illustration of the first method of carrying out the invention. This modification of the process permitsthe production of a lustrous pattern upon a dull background or vice versa.
2. The alkali solution, mixed with a suitable thickening agent (such as starch, denatured albumen, a cellulose-hydrate which is soluble in alkali, an alkylor oxyalkyl-cellulose derivative which is soluble in alkai or in water, or a cellulose-hydroxyparaflinmonocarboxylic acid or the like), is printed in any desired pattern on the woven material, which is then treated with an inorganic ester of a monohydric alcohol, advantageously with a dialkyl sulphate, an alkyl halide or an aralkyl halide as already described. The.
ell'ects obtained resemble those obtained according to l.
3. After treatment with alkali solution and if necessary after drying, the material is printed with a reserve which prevents, either mechanically or chemically, the reaction between the alkali-cellulose and the inorganic ester. There may be used for this purpose,
acid, albumen, kaolin, zinc-fi white, or the like. There may also be added for example, an
to the reserve paste a dyestuif or pigment. After printing with the reserve the material is treated with the inorganic ester as in the first method of carrying out the invention, and is then treated with an acid or salt, and dried. This method yields strongly lustrous efl'ects on a less lustrous background, or vice versa.
4. Pattern effects may also be produced by impregnating the woven material with alkali solution according to the first method of can rying out the invention, then, if necessary,
after previously drying the material, printing it with an inorganic ester of a monohydric alcohol, advantageously with a dialkvl sulphate, an alkyl halide, or an aralkyl halide, dissolved or suspended in a suitable thickening medium (for example British gum, starch or dextrin) with or without the addition of a dyestufi', and then finishing the material according to the first method of carrying out the invention. Highly lustrous effects on a less lustrous background may thus be obtained.
5. An inorganic ester of a monohydric alcohol, advantageously a dialkyl sulphate, an alkyl halide or an aralkyl halide, in the form of a solution or suspension, is printed on the woven material with the aid of a thickening agent, and the material is then subjected, with or without drying, to the action of alkali solution. The effects are similar to those obtained in 3 and 4.
The following examples illustrate the invention, the parts being by weight 1. (a) Bleached or unbleached cotton fabric or yarn is treated with caustic soda solution of 25-40 per cent. strength for a period of from 5 minutes to 12 hours at room temperature, and the excess of the solution removed by wringing or centrifuging, until the material retains about 2 -3 times its weight or any other desired proportion, of the solution. The impregnated material is then treated either immediately or after it has been allowed to stand for 3-72 hours, with dimethyLSulphate, diethyl-sulphate, ethyl iodide, methyl iodide, ethyl bromide or benzyl chloride, either alone, or in the form of a solution bf -50 per cent. strength in benzol or chloroform or carbon tetrachloride or in alcohol or the like, or in the form of a suspension of 10-50 per cent. strength in a solution of British gum of -25 per cent. strength. The yarn or fabric may be impregnated or coated on one or both sides with the ester, or the solution or suspension thereof, or the ester, or the solution or suspension thereof may be rolled on to or into the textile material. There is practically no limit to the quantity of the ester which may be incorporated with the yarn or fabric which has been impregnated with caustic soda solution. For reasons of economy, however, it is advisable'to use a quantity equal to not more than to 1 times the Weight of the cotton goods, particularly as excellent effects may be obtained with this amount or even with a smaller amount. After the material has been in contact with the inorganic ester for a short period (for example 10 minutes), or for a longer period (for example 12 hours), it is washed and dried or introduced into a dilute solution (for example of 10-20 per cent. strength) of sulphuric or acetic acid, or into a solution ofammonium chloride or ammonium sulphate of 20-30-per cent.
as 5 minutes), or for a longer period (such as several-hours), and is then washed and dried. The fixing material may be applied to the fabric by sprinkling, spraying or the like.
During the foregoing operations, the fabric or yarn should be stretched for at least a part of the time, for instance, during the action of the alkali solution. If the duration of-the action of the alkali solution and of the ester is not too long, the material may be in the stretched condition throughout all the operations. It may,- however, be sretched after it has been impregnated with the alkali solution, and remain stretched during the whole or a portion of the treatment with the ester, and if necessary during the treatment with the acid or salt. The textile material may also be stretched during the washing operation, though this is ad-v vantageous only in respect of the silk-like lustre.
According to the process described in this example, there is obtgnbd a high-grade, silk-like lustre, and a pleasing finish o elastic feel.
(6) The procedure is as'in a, with the exception that the action of the inorganic ester is carried out at raised temperature. For this purpose, the material which has been impregnated with caustic soda solution and brought into contact with the ester is maintained for 10 minutes to 1 hour at a temperature .of 50-100 (1., for instance at 80 C.
(a) The procedure is as in a or b, with the exception that the caustic soda solution used is of 18-20. per cent. strength instead of -40 per cent. strength. The final product has a very beautiful silky lustre.
2. Bleached or unbleached cotton fabric or yarn is impregnated with a solution of 10 per cent. strength of di-methyl sulphate, di-ethyl sulphate, ethyl iodide, methyl iodide or ethyl bromide in alcohol or benzol The material impregnated sired, after removal of the excess by squeezingor centrifugin into a solution of caustic soda solution of allowed to remain in contact with the solution for a period of from 10 minutes to 2 hours and then finished as described in Example .1 (a). The fabric may be stretched ples 1 (a) to 1 (c), with the exceptionthat' during or after the treatment with the al- ;kali solution. A silky lustre is produced.
3. The procedure is as in any of Examinstead of aqueous caustic soda solution of 30-40 per cent. strength,
4. The procedure is exactly as in any of the preceding examples, with the exceptlon that the material is treated with strong sulphuric acid before being treated according to the invention. When sulphuric acid of 49-50 Baum specific gravity is used, the treatment with the acid may occur at room temperature'for a period of from several seconds to several minutes, or even longer.
.When a stronger acid is used, for example,
of 52-54 Baum specific gravity, the treatment may occupy only several seconds at room temperature, but a longer period if the acid be cooled to 0 C. or below.
The treatment with sulphuric acid may also precede mercerization of the fabric, for
example, with caustic soda solution of 10.
per cent. strength at a low temperature or with a stronger caustic soda solution, for
instance, one of 18 10 per cent. strength at The expression textile material in the .description and claims means, where the context permits, all vegetable fibres such as,
flax, linen, hemp, ramle, jute and articularly cotton, and the like, in the orm of fabric of the pure vegetable product (such as pure cotton fabric) or mixed fabric, or yarn which, if desired, may be in the form of skeins, cops or warps.
The expression precipitating agent means acids, salts, acid salts, m xtures of acids and salts, in short all precipitatin agents known in the viscose industry as we as organic acids or aqueous solutions there of, alcohols, tannic acids, and. formaldehyde.
I claim: I v I 1. A process for improving vegetable textile material which comprises treating it with an inorganic ester of a monohydric alcohol in the presence of alkali. 2. A process for improving vegetable tex tile material which comprises treating it with an alkali solution, and thereafter reactin on .120
it with an inorganic ester of a monohy ric alcohol.
3. A process for improving vegetable textile material which comprises treating it with an alkali solution and thereafter acting on it with an inorganic ester of a monohydric alcohol in presence of at least a portion of the alkali solution used in the treatment.
4. A process for improving vegetable textile material, which comprlses treating it with an alkali solution, and thereafter acting llti tlti
till
on it with an inorganic ester of a monohydric alcohol in presence of the alkali solution remaining in the material.
5. A process for improving vegetable textile material, which comprises treating it with an alkali solution and after removing at least a portion of the water by drying, reacting on it with an inorganic ester of a monohydric alcohol.
6. A process for improving vegetable textile material, which comprises treating it' with an alkali solution, andthereafter'reacting on at least one side with an inorganic ester of a monohydric alcohol.
7. A process for improving vegetable textile material, which comprises treating it with a solution of an alkali and thereafter reacting on at least one side with an inorganic ester of a monohydric alcohol mixed with a thickening agent.
8. A process for improving vegetable textile material, which comprises treating it with an alkali solution and reacting on it at certain parts with an inorganic ester of a monohydric alcohol.
9. A process for improving vegetable textile material, which comprises treating it with a solution of an alkali and printing it in the presence of alkali with an inorganic ester of a monohydric alcohol mixed with a thickening agent.
10. A process for improving vegetable textile material, which comprises treating it at certain parts with an alkali solution and thereafter reacting on it with an inorganic ester of a monohydric alcohol.
11. The process for improving vegetable textile material which comprises treating it with an inorganic ester of a monohydric alcohol at least at certain parts in the presence of a solution containing alkali metal hydroxide.
12. A process for improving vegetable textile material, which comprises acting on it at a raised temperature, in the presence of an alkali, with an inorganic ester of a monohydric alcohol.
13. A process for improving vegetable textile material, which comprises treating it with an alkali solution and thereafter reacting on it at a raised temperature with an inorganic ester of a monohydric alcohol.
let. A process for improving vegetable textile material, which comprises acting on it in presence of an alkali with an inorganic ester of a monohydric alcohol, thereafter treating it with a precipitating agent and washing it.
15. A process for improving vegetable textile material, which comprises treating it with an alkali solution, thereafter reacting on it with an inorganic ester of a monoliydric alcohol, and thereafter treating it with a precipitating agent and washing it.
it. A process for improving vegetable textile material, which comprises acting on it in'presence of an alkali with an inorganic ester of a monohydric alcohol and stretching the material during at least a portion of the process.
17. A process for improvingvegetable textile material, which comprises treating it with an alkali solution, thereafter reacting on it with an inorganic ester of a monohydric alcohol, and stretching the material during at least a portion of the process.
18. A process for improving vegetable textile material, which comprises treating it with an alkali solui-ion, thereafter reacting on it with an inorganic ester of a monohydric alcohol, thereafter treating it with a precipitating agent, and washing it, and stretching the material during at least a portion of the process.
19. A process for improving vegetable textile material, which comprises treating it with a dialkyl sulphatein presence of alkali.
20. A process for improving vegetable textile material, which comprises treating it with an alkali solution, and thereafter reacting on it with a dialkyl sulphate.
. 21. A process for improving vegetable textile material, which comprises treating it with an alkali solution and thereafter acting on it with a dialkyl sulphate in presence of at least a portion of the alkali solution used in the treatment.
22. A process for improving vegetable textile material, which comprises treating it with an alkali solution, and thereafter acting on it with a dialkyl sulphate in presence of the alkali solution remaining in the material.
23. A process for improving vegetable textile material, which comprises treating it with an alkali solution and after removing at least a portion of the water by drying, reacting on it with a dialkyl sulphate.
24:. A process for improving vegetable textile material, which comprises treating it with an alkali solution and thereafter reacting on it with a dialkyl sulphate in presence of a thickening agent.
25. A process for improving vegetable. textile material, which comprises treating it with an alkali solution and thereafter reacting on at least one side with a dialkyl sulphate.
26. A process for improving vegetable textile material, which comprises treating it with a solution of an alkali and thereafter reacting it on at least one side with a dialkyl sulphate mixed with a thickening agent.
27. A process for improving vegetable textile material, which comprises treating it with an alkali solution and reacting on it at certain parts with a dialkyl sulphate.
28. A process for improving vegetable textile. material, which comprises treating it I with a solution of an alkali and printing it Bil 4 an alkali solution, thereafter reacting in the presence of with a dialkyl sulphate mixed with a thickening agent.
29. A process for improving vegetable textile material, which comprises treating it at certain parts with an alkali solution and thereafter reacting on it with a dialkyl sulphate.
30. A process for improving vegetable tex- I tile material, which comprises treating it an alkali with a dialkyl sulphate.
32. A process for improving vegetable textile material, which comprises treating it with an alkali solution and thereafter reactinon it at a raised temperature with a dia kyl sulphate.
33. A process for improving vegetable textile material, which comprises acting on it in presence of an alkali with a dialkyl sulphate, thereafter treating it with a precipitating agent and washing it.
34. A process for improving vegetable tex tile material, which comprises treating it with an alkali solution, thereafter reacting on it with a dialkyl sulphate, thereafter treating it with. a precipitating agent and washing it.
35. A process for improving vegetable textile material, which comprises acting on it in presence of an alkali with a dialkyl sulphate and stretching the material during at least a portion of. the process.
36. A process for improving vegetable textile material, which comprises treating it with an alkali solution, thereafter reacting on it with a dialkyl sul hate, and stretching the material during at east a portion of the process.
37. A process for improving vegetable textile material, which comprises treating it with on it with a d-ialkyl sulphate, then treating it with a precipitating agent, and washing it, and stretching the material during at least a portion of the process.
38. As new products, silk-like lustrous vegetable textile materials, which contain a derivative of cellulose in which a portion of the hydrogen of the cellulose has been exchanged for the residue of a monohydric alv cohol.
39. As new products, silk-like lustrous, ve etable textile materials which contain an a l derivative of cellulose.
40. As new products, silk-like lustrous, vegetable textile materials which contain an aralkyl derivative of cellulose.
41. The process of treating vegetable tex- I
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT234847X | 1924-05-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1800944A true US1800944A (en) | 1931-04-14 |
Family
ID=3669987
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US31446A Expired - Lifetime US1800944A (en) | 1924-05-30 | 1925-05-19 | Process for improving vegetable textile material |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US1800944A (en) |
| DE (1) | DE498884C (en) |
| GB (1) | GB234847A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2426561A (en) * | 1944-12-18 | 1947-08-26 | Pacific Mills | Process for producing absorbent cellulosic material |
| US2439865A (en) * | 1944-03-01 | 1948-04-20 | Celanese Corp | Manufacture of water-soluble textile materials |
| US2545492A (en) * | 1948-01-23 | 1951-03-20 | Reid John David | Fabrics of a long chain amino-ethoxy cellulose and the method of making the same |
| US2990234A (en) * | 1959-03-13 | 1961-06-27 | Klein Elias | Production of strong, rot-resistant benzyl cellulose fibers |
| US3396530A (en) * | 1961-11-13 | 1968-08-13 | Heberlein Patent Corp | Method for producing permanently crimped, elastic chemically modified cotton yarns |
| US3396528A (en) * | 1962-06-21 | 1968-08-13 | Heberlein Patent Corp | Permanentlay crimped, elastic chemically modified cotton yarns |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE752308C (en) * | 1938-10-28 | 1952-10-13 | Siemens Schuckertwerke A G | Process for reducing the water absorbency of paper |
-
1925
- 1925-05-09 DE DEL63104D patent/DE498884C/en not_active Expired
- 1925-05-19 US US31446A patent/US1800944A/en not_active Expired - Lifetime
- 1925-05-29 GB GB14225/25A patent/GB234847A/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2439865A (en) * | 1944-03-01 | 1948-04-20 | Celanese Corp | Manufacture of water-soluble textile materials |
| US2426561A (en) * | 1944-12-18 | 1947-08-26 | Pacific Mills | Process for producing absorbent cellulosic material |
| US2545492A (en) * | 1948-01-23 | 1951-03-20 | Reid John David | Fabrics of a long chain amino-ethoxy cellulose and the method of making the same |
| US2990234A (en) * | 1959-03-13 | 1961-06-27 | Klein Elias | Production of strong, rot-resistant benzyl cellulose fibers |
| US3396530A (en) * | 1961-11-13 | 1968-08-13 | Heberlein Patent Corp | Method for producing permanently crimped, elastic chemically modified cotton yarns |
| US3396528A (en) * | 1962-06-21 | 1968-08-13 | Heberlein Patent Corp | Permanentlay crimped, elastic chemically modified cotton yarns |
Also Published As
| Publication number | Publication date |
|---|---|
| DE498884C (en) | 1930-06-03 |
| GB234847A (en) | 1926-01-28 |
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