US2289039A - Process for making textile fibers - Google Patents
Process for making textile fibers Download PDFInfo
- Publication number
- US2289039A US2289039A US279040A US27904039A US2289039A US 2289039 A US2289039 A US 2289039A US 279040 A US279040 A US 279040A US 27904039 A US27904039 A US 27904039A US 2289039 A US2289039 A US 2289039A
- Authority
- US
- United States
- Prior art keywords
- fibers
- alkali
- cellulose
- textile
- salt
- 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
- 239000000835 fiber Substances 0.000 title description 86
- 239000004753 textile Substances 0.000 title description 22
- 238000000034 method Methods 0.000 title description 12
- 239000003513 alkali Substances 0.000 description 38
- 150000003839 salts Chemical class 0.000 description 31
- 229920003086 cellulose ether Polymers 0.000 description 24
- 229920002678 cellulose Polymers 0.000 description 23
- 239000001913 cellulose Substances 0.000 description 22
- 238000006243 chemical reaction Methods 0.000 description 12
- 239000003795 chemical substances by application Substances 0.000 description 11
- 229910052783 alkali metal Inorganic materials 0.000 description 10
- 150000001340 alkali metals Chemical class 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 238000009960 carding Methods 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- 238000006266 etherification reaction Methods 0.000 description 8
- 239000003518 caustics Substances 0.000 description 7
- 229920000742 Cotton Polymers 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 235000015424 sodium Nutrition 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 235000004431 Linum usitatissimum Nutrition 0.000 description 2
- 240000006240 Linum usitatissimum Species 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 230000003113 alkalizing effect Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229940117927 ethylene oxide Drugs 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- -1 for ex ample Chemical class 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 239000012991 xanthate Substances 0.000 description 2
- GAWAYYRQGQZKCR-REOHCLBHSA-N (S)-2-chloropropanoic acid Chemical compound C[C@H](Cl)C(O)=O GAWAYYRQGQZKCR-REOHCLBHSA-N 0.000 description 1
- YYTSGNJTASLUOY-UHFFFAOYSA-N 1-chloropropan-2-ol Chemical compound CC(O)CCl YYTSGNJTASLUOY-UHFFFAOYSA-N 0.000 description 1
- 244000198134 Agave sisalana Species 0.000 description 1
- 240000008564 Boehmeria nivea Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 244000146553 Ceiba pentandra Species 0.000 description 1
- 235000003301 Ceiba pentandra Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 240000000491 Corchorus aestuans Species 0.000 description 1
- 235000011777 Corchorus aestuans Nutrition 0.000 description 1
- 235000010862 Corchorus capsularis Nutrition 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 241000219146 Gossypium Species 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 239000012084 conversion product Substances 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- ILHIHKRJJMKBEE-UHFFFAOYSA-N hydroperoxyethane Chemical group CCOO ILHIHKRJJMKBEE-UHFFFAOYSA-N 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 229910001867 inorganic solvent Inorganic materials 0.000 description 1
- 239000003049 inorganic solvent Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- PHZLMBHDXVLRIX-UHFFFAOYSA-M potassium lactate Chemical compound [K+].CC(O)C([O-])=O PHZLMBHDXVLRIX-UHFFFAOYSA-M 0.000 description 1
- 239000001521 potassium lactate Substances 0.000 description 1
- 235000011085 potassium lactate Nutrition 0.000 description 1
- 229960001304 potassium lactate Drugs 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 239000001120 potassium sulphate Substances 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Inorganic materials [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L sodium sulphate Substances [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000005418 vegetable material Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 210000002268 wool Anatomy 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
- D06M13/244—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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B11/00—Preparation of cellulose ethers
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/07—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof
- D06M11/11—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with halogens; with halogen acids or salts thereof; with oxides or oxyacids of halogens or salts thereof with halogen acids or salts thereof
- D06M11/13—Ammonium halides or halides of elements of Groups 1 or 11 of the Periodic Table
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/51—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with sulfur, selenium, tellurium, polonium or compounds thereof
- D06M11/55—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with sulfur, selenium, tellurium, polonium or compounds thereof with sulfur trioxide; with sulfuric acid or thiosulfuric acid or their salts
-
- 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
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/58—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with nitrogen or compounds thereof, e.g. with nitrides
- D06M11/64—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with nitrogen or compounds thereof, e.g. with nitrides with nitrogen oxides; with oxyacids of nitrogen or their salts
-
- 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
- D06M13/10—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 oxygen
- D06M13/11—Compounds containing epoxy groups or precursors thereof
-
- 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
- D06M13/10—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 oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/188—Monocarboxylic acids; Anhydrides, halides or salts thereof
-
- 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
- D06M13/10—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 oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/207—Substituted carboxylic acids, e.g. by hydroxy or keto groups; Anhydrides, halides or salts thereof
-
- 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
- D06M13/10—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 oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/207—Substituted carboxylic acids, e.g. by hydroxy or keto groups; Anhydrides, halides or salts thereof
- D06M13/21—Halogenated carboxylic acids; Anhydrides, halides or salts thereof
Definitions
- the present invention relates in general to textile'fibers whichare composed in whole or in part of a cellulose ether and in particular to a process for the conversion of cellulose textile fibers into textile fibers composed in whole or in part of a cellulose ether which is soluble in water or aqueous alkali solutions.
- coalesced fibers cannot be readily separated by carding, combing and the like.
- textile fibers comprising The fibers I 1 ing alkali-soluble cellulose ethers itis desirable to obtain a product which is readily soluble in dilute caustic alkali solution of 2 to 3 percent strength when a mixture of the fibers and caustic alkali is cooled to 0 C. so that the use of cellulose ether fibers in admixture with rayon fibers which are not resistant to strong alkalies is rendered difficult or impracticable.
- the-chief object of the present invention is to convert celluloslc fibers of texcompletely into a cellulose ether in the form of loose fibers which can be readily separated b carding, combing and the like.
- natural or artificial cellulosic fibers of textile-making length are superficially, partially or completely etherified in the presence of alkali and also in the presence of a substantial quantity of an added water-soluble inert salt, the reaction being carried out until the cellulose of the fibers is converted to a water-soluble or alkali-soluble cellulose ether and the fibers are then purified, preferably by washing the fibers with a solution of a water-soluble inert salt and then drying the fibers.
- the alkali remaining in the reaction mass l is preferably neutralized by dumping the product into a large quantity of a dilute solution of any etherification more uniform.
- the individual fibers of the product can be readily separated by carding, combing and thelike. a
- the expression cellulosic fibers as used here- 7 in is intended to designate both natural and artificial fibers and filaments of all kinds, which are suitable for conversion inthe process of the.
- suitable cellulosic fibers which may be treated in the present invention: naturally-occurring cellulose fibers such as those derived from cotton, kapok, flax; hemp, jute, sisal, ramie, cocoanut, straw, woodand the like; cellulose hydrate fibers as derived from any source such, for example, as from the regeneration of cellulose xanthates, de-esterification of cellulose esters, or by precipitation from solutions of cellulose in organic or inorganic solvents; textile fibers com;- prising cellulose conversion products such,;for example, as oxy-cellulose, hydro-cellulose, and the like; cellulose ethers such, for example, as c'ellu 'lose ether xanthates ofa low degreecf etherifi- I cation, cellulose mixed ether-esters, and the like.
- naturally-occurring cellulose fibers such as those derived from cotton, kapok, flax; hemp, jute, sisal, ram
- the materials may be subjected to any suitable purification as an alkyl ester of an inorganic acid, for ex ample, alkyl halides such as methyl chloride, ethyl chloride, ethyl bromide and di-me'thyl sulphate, and alkyl half esters of sulphuric acid; also an hydroxy-alkylating agent such, for example, as a halogen derivative of a polyhydric alcohol, such as ethylene chlorhydrin, propylene chlorhydrin, epichlorhydrin, and alkylene oxides,
- alkyl ester of an inorganic acid for ex ample, alkyl halides such as methyl chloride, ethyl chloride, ethyl bromide and di-me'thyl sulphate, and alkyl half esters of sulphuric acid; also an hydroxy-alkylating agent such, for example, as a halogen derivative of a polyhydric alcohol, such as ethylene chlor
- ethylene oxide, propylene oxide and glycides such as ethylene oxide, propylene oxide and glycides; also a' halogenated fatty acid or its salt or ester which converts the cellulosic material into a hydroxy acid ether of cellulose, suitable an etherifying agent derived from an acid in a agents being chloroacetic acid, chloropropionic acid, and the like.
- cellulose ether as -used herein, is intended to include, any cellulose ether produced by reacting on cellulose with one or more of the mentioned reagents or their chemical equivalents.
- the salt employed in the present process may comprise any water-soluble inert salt of an alkali metal with an inorganic or organic acid such, for example, as sodium or potassium chloride, sodium or potassium sulphate, sodium or potassium nitrate, and the like, sodium or potassium acetate, sodium or potassium citrate, sodium .or potassium lactate.
- an inorganic or organic acid such as sodium or potassium chloride, sodium or potassium sulphate, sodium or potassium nitrate, and the like, sodium or potassium acetate, sodium or potassium citrate, sodium .or potassium lactate.
- inert indicates that a salt is to be selected which is inert with respect to alkali or the etherifying agent employed in the process, and which does not swell or gelatinize the cellulosic raw material or the cellulose ether produced therefrom under the conditions of reaction.
- concentration of the salt to be used in a particular case will depend, inter alia, upon the quantity of alkali and water present during the steeping or reaction, and upon the nature and character of the cellulosic fibers and of the product produced. It is merely necessary that a suflicient quantity be present to'retard or substantially prevent gelatinization of, the cellulosic raw material or of,
- the salt may be added to the cellulosic raw material prior tov or during the steeping or mercerizing of the initial raw cellulose with alkali, or may be dissolved in the alkali which is employed for such steeping or mercerizing; and/or the salt may be present during the reaction by which the cellulosic fibers are converted to the cellulose ether. present during steeping or mercerizing, the quantity which remains,
- salt may be added to the liquors which are employed for purifying and washing the product.
- an inorganic salt may be pro-.
- a vegetable material in the form of loose separable fibers of textile making length is converted into alkalisoluble cellulose ether by alkalizing the vegetable fiber with a dilute alkali solution and etherifying the alkalized fibers with a suitable etherifying agent in an alkaline medium in the presence of.
- a water-soluble inert salt a water-soluble inert salt.
- concentration of the alkali and the temperature of the alkalizing treatment should be so correlated as to soften but not to gelatinize the. fibers.
- An alkali concentration of from 10 to 20 per cent at a temperature of from 15 to 20 C. is suitable when the water-soluble inert salt is present in an amount of from 10 to 20 per cent based on the weight 'of the cellulose. With lower concentration of alkali the quantity of salt may be reduced.
- the mole ratio by weight of dry cellulose (061-11005) to solid alkali calculated as sodium hydroxide preferably should not exceed 1:15, the Water present during reaction being such'that the concentration of alkali is not above about 20 per cent, preferably not above 10 per cent when etherifying cellulose hydrate fibers and not above 20 per cent when etherifying natural-occurring cellulose fibers, and the concentration of salt being sufficient to prevent the gelatinization or sticking together of the fibers during reaction.
- the cellulose ether fibers are removed from the autoclave and washed in boiling water until free of alkali and salt and. thereafter treated with, hot dilute oxalic acid to remove color due to iron and finally washed until free of acid, extracted in a centrifuge and dried.
- the product is a hydroxy ethyl ether of cellulose in the form of a, textilefiber which is readily soluble in 3%caustic alkali at 0 C.
- Example II - parts of dry staple cotton fiber of textile-making length, which has been purified by a suitable pretreatment of non-cellulosic ingredients are alkalized with 1000 parts of an 18 per cent aqueous solution of sodium hydroxide containing 8 per cent sodium chloride based on the weight of dry cellulose for hour at room temperature until the cotton mass is thoroughly saturated with the alkali. The treated cotton is then centrifuged until the weight of the alkali solution remaining is substantially equal to twice the weight of the dry cotton. The centrifuged material is etherified with 15 per cent by weight of ethyleneoxide at 25' C. in a closed container in the presence of at least per cent of sodium chloride based on the weight of dry cellulose. At the end of about 12 hours, the reaction is substantially complete.
- the excess etherifying agent is withdrawn and the product is washed with hot water until substantially free of alkali and salt.
- the purified fiber is dried by passing a stream of warm air upwardly therethrough until the fibers are substantially dry to the touch.
- the product consists of a mass of fibers of textile-making length comprising alkali-soluble cellulose ether, the individual fibers being separable one from another by carding, combing, etc.
- the fibers produced by the present invention may be used alone or in admixture with other textile making fibers, such as cotton, flax or wool in the formation of textiles including felts, yarns, threads, cords, fabrics and woven textile structures .of all kinds.
- the products have a wool-like feel, warmth and appearance.
- the textile fibers of the present invention are particularly adapted for use as coalescing fibers.
- a yarn formed from the. fibers of the invention may be treated with a solvent such as an aqueous alkali solution of sufiicient concentration to superficially, partially or substantially gelatinize the fibers and render them adhesive, whereby the, yarn may then be-squeezed to cause the fibers to coalesce and the alkali neuseparated by carding, combing, and the like.
- a process for-the production of textile fibers which comprises treating a mass of loose cellulosic fibers of textile-making length with an etherifying agent in the presence of an aqueous solution of an alkali capable of forming an alkali cellulose thereof, continuing the etherification until the cellulose ether fibers produced are soluble in caustic alkali, the etherification betralized with an acid to fix the fibers in the coalesced condition.
- the fibers of the present invention may be used as potentially adhesive fibers and thus after being admixed with non-adhesive textile fibers, they may be formed into yarns, threads cords, fabrics and other textiles and the cellulose ether fibers rendered adhesive by a suitable solvent to produce stillened textiles as disclosed and claimed in prior British Patent No. 501,436.
- a process for the production of textile fibers which comprises treating a mass or loose cellulosic fibers of textile-making length with an etherifying agent in the presence of an aqueous solution of an alkali capable of forming an cation until the cellulose ether fibers produced are'soluble in caustic alkali, the etherification being carried out in the presence of a quantity of a water-soluble inert salt of an alkali metal suiifllcient to prevent the sticking together of the alkali cellulose thereof, continuing the etherifiing carriedout in the presence of a quantity of a water-soluble inert salt of an alkali metal sufiicient to prevent the sticking together of the fibers, washing the treated fibers with an aqueous solution of a water-soluble inert salt of an alkali metal in sufllcient quantity to prevent gelatinization of the fibers to obtain alkali-soluble cellulose ether fibers of textile-making lengthwhich fibers can be readily separated by carding, combing, and the like
- a process for the production of textile fibers which comprises treating a mass of loose cellulosic fibers of textile-making length with an etherifying agent in the presence of an aqueous solution of an alkali capable of forming an alkali cellulose thereof, continuing the etherification until the cellulose ether fibers produced are soluble in caustic alkali, the etherification being carried out in the presence of a quantity of a water-soluble inert salt of an alkali metal sufiicient to prevent the sticking together of the fibers, washing the treated fibers with an aqueous solution of a water-soluble inert salt of an alkali metal in sufiicient quantity to prevent gelatinization of the fibers to obtain alkali-soluble cellulose ether fibers of textile-making length which fibers can be readily separated by carding, comb- -ing,,and the like, and drying the fibers by passing a current of warm air upwardly through the mass of fibers.
- a process for the production of textile fibers which comprises treating a mass of loose cellulosic fibers of textile-making length with an alkaline swelling agent in the presence of a quantity of water-soluble inert salt of an alkali metal sufiicient to prevent the gelatinization of the fibers,- treating the swollen fibers with an etherifying agent in the presence of an aqueous solution of an alkali capable of forming an alkali cellulose thereof, continuing the etherification until the cellulose ether fibers produced are soluble in caustic alkali, the etherifioation being carried out inthe presenceof a quantity of a alkaline swelling agent in the presence of a water soluble inert salt of an alkali metal and thereafter treating the swollen fibers with an ether-iwater-soluble inert salt or an alkali metal sunlcient to prevent the sticking together or the fibers and washing the fibers with an aqueous solution containing a water-soluble inert salt of an alkali
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Description
MM July 1, 1942 raocass FOR MAKING 'rnx'rma FIBERS Frank, H. Reichel, Fredericksburg, Va., assignor to Sylvania Industrial Corporation, Fredericksburg, Va., a corporation of Virginia No Drawing. Application June 14, 1939, Serial No. 279,940. In Great Britain June 14, 1938 '5 Claims.
The present invention relates in general to textile'fibers whichare composed in whole or in part of a cellulose ether and in particular to a process for the conversion of cellulose textile fibers into textile fibers composed in whole or in part of a cellulose ether which is soluble in water or aqueous alkali solutions.
In the prior specification Serial No. 218,220 filed July 8, 1938, there is disclosed for the first time a method of preparing textile fibers formed in whole or in part of a cellulose ether. Among the uses of such fibers are many valuable technical applications in the textile and cordage arts in which it is necessary to card, comb and spin the fibers. For such uses it is essential that the fibers are capable of being freely separated by the carding and combing operations. of the present invention are prepared by etherifying cellulosic textile fibers in the presence of alkali. The alkali tends under certain conditions of high concentration and low temperature to cause the etherified fibers to gelatinize sufliciently t,o-stlck together which interferes with their purification, drying and subsequent use. In particular the coalesced fibers cannot be readily separated by carding, combing and the like. Further in the production of textile fibers compris- The fibers I 1 ing alkali-soluble cellulose ethers itis desirable to obtain a product which is readily soluble in dilute caustic alkali solution of 2 to 3 percent strength when a mixture of the fibers and caustic alkali is cooled to 0 C. so that the use of cellulose ether fibers in admixture with rayon fibers which are not resistant to strong alkalies is rendered difficult or impracticable.
Accordingly, the-chief object of the present invention is to convert celluloslc fibers of texcompletely into a cellulose ether in the form of loose fibers which can be readily separated b carding, combing and the like.
According to the present invention, natural or artificial cellulosic fibers of textile-making length are superficially, partially or completely etherified in the presence of alkali and also in the presence of a substantial quantity of an added water-soluble inert salt, the reaction being carried out until the cellulose of the fibers is converted to a water-soluble or alkali-soluble cellulose ether and the fibers are then purified, preferably by washing the fibers with a solution of a water-soluble inert salt and then drying the fibers. The alkali remaining in the reaction mass l is preferably neutralized by dumping the product into a large quantity of a dilute solution of any etherification more uniform. The individual fibers of the product can be readily separated by carding, combing and thelike. a The expression cellulosic fibers as used here- 7 in, is intended to designate both natural and artificial fibers and filaments of all kinds, which are suitable for conversion inthe process of the.
invention. 7
By way of illustrating, but not by way of limit-.
ing the invention, the following-are examples oi.
suitable cellulosic fibers which may be treated in the present invention: naturally-occurring cellulose fibers such as those derived from cotton, kapok, flax; hemp, jute, sisal, ramie, cocoanut, straw, woodand the like; cellulose hydrate fibers as derived from any source such, for example, as from the regeneration of cellulose xanthates, de-esterification of cellulose esters, or by precipitation from solutions of cellulose in organic or inorganic solvents; textile fibers com;- prising cellulose conversion products such,;for example, as oxy-cellulose, hydro-cellulose, and the like; cellulose ethers such, for example, as c'ellu 'lose ether xanthates ofa low degreecf etherifi- I cation, cellulose mixed ether-esters, and the like. Y Y tile-making length superficially, partially or In the preparation of the cellulosic raw material ior treatment in the process, the materials may be subjected to any suitable purification as an alkyl ester of an inorganic acid, for ex ample, alkyl halides such as methyl chloride, ethyl chloride, ethyl bromide and di-me'thyl sulphate, and alkyl half esters of sulphuric acid; also an hydroxy-alkylating agent such, for example, as a halogen derivative of a polyhydric alcohol, such as ethylene chlorhydrin, propylene chlorhydrin, epichlorhydrin, and alkylene oxides,
such as ethylene oxide, propylene oxide and glycides; also a' halogenated fatty acid or its salt or ester which converts the cellulosic material into a hydroxy acid ether of cellulose, suitable an etherifying agent derived from an acid in a agents being chloroacetic acid, chloropropionic acid, and the like.
The expression cellulose ether, as -used herein, is intended to include, any cellulose ether produced by reacting on cellulose with one or more of the mentioned reagents or their chemical equivalents. i
The salt employed in the present process may comprise any water-soluble inert salt of an alkali metal with an inorganic or organic acid such, for example, as sodium or potassium chloride, sodium or potassium sulphate, sodium or potassium nitrate, and the like, sodium or potassium acetate, sodium or potassium citrate, sodium .or potassium lactate.
The expression inert as applied to the salt, indicates that a salt is to be selected which is inert with respect to alkali or the etherifying agent employed in the process, and which does not swell or gelatinize the cellulosic raw material or the cellulose ether produced therefrom under the conditions of reaction. The concentration of the salt to be used in a particular case will depend, inter alia, upon the quantity of alkali and water present during the steeping or reaction, and upon the nature and character of the cellulosic fibers and of the product produced. It is merely necessary that a suflicient quantity be present to'retard or substantially prevent gelatinization of, the cellulosic raw material or of,
The salt may be added to the cellulosic raw material prior tov or during the steeping or mercerizing of the initial raw cellulose with alkali, or may be dissolved in the alkali which is employed for such steeping or mercerizing; and/or the salt may be present during the reaction by which the cellulosic fibers are converted to the cellulose ether. present during steeping or mercerizing, the quantity which remains,
results during the chemical reaction but, if not, additional salt may be added to the reaction mixture. In addition, the salt may be added to the liquors which are employed for purifying and washing the product.
It is to be understood that the conversion of the cellulosic raw material to the cellulose ether is carried out under suitable conditions of ,concentration and quality of reactants, temperature,
' pressure and other variables as known to those skilled in the art, and such processes, per se,.
when not employing a salt as herein described fomn no part of the present invention.
When a cellulosic material isethe'rified with When the salt is after pressing or centrifuging, may be suificient. to effect the novel reaction medium containing an inorganic alkali,
it is obvious that an inorganic salt may be pro-.
duced as a by-product. It is to be understood that the salt thus produced as a by-product is not sufiicient to prevent the; gelatinization or solution of the product and, therefore, does not effect the new and novel results obtained by the use of additional quantities of a water-soluble inert salt as provided in the present invention.
To prepare a fibrous material suitable for use in the textile and cordage arts, a vegetable material in the form of loose separable fibers of textile making length is converted into alkalisoluble cellulose ether by alkalizing the vegetable fiber with a dilute alkali solution and etherifying the alkalized fibers with a suitable etherifying agent in an alkaline medium in the presence of.
a water-soluble inert salt. The concentration of the alkali and the temperature of the alkalizing treatment should be so correlated as to soften but not to gelatinize the. fibers. An alkali concentration of from 10 to 20 per cent at a temperature of from 15 to 20 C. is suitable when the water-soluble inert salt is present in an amount of from 10 to 20 per cent based on the weight 'of the cellulose. With lower concentration of alkali the quantity of salt may be reduced. During the step of etherification, the mole ratio by weight of dry cellulose (061-11005) to solid alkali calculated as sodium hydroxide preferably should not exceed 1:15, the Water present during reaction being such'that the concentration of alkali is not above about 20 per cent, preferably not above 10 per cent when etherifying cellulose hydrate fibers and not above 20 per cent when etherifying natural-occurring cellulose fibers, and the concentration of salt being sufficient to prevent the gelatinization or sticking together of the fibers during reaction.
By way of illustrating, but not by way of limit ing the scope of the invention, there may be given the following examples but the invention duced. is aged for 16 hours at from 20 to 21 C.
and then placed in an autoclave. To the autoclave 82 grams (20 per cent by weight) of ethylene chlorhydrin are added, the autoclave then being rotated for about 5 hours at a temperature being maintained at from 20 to 26 C.
After about 5 hours, the cellulose ether fibers are removed from the autoclave and washed in boiling water until free of alkali and salt and. thereafter treated with, hot dilute oxalic acid to remove color due to iron and finally washed until free of acid, extracted in a centrifuge and dried. The product is a hydroxy ethyl ether of cellulose in the form of a, textilefiber which is readily soluble in 3%caustic alkali at 0 C.
Example II.- parts of dry staple cotton fiber of textile-making length, which has been purified by a suitable pretreatment of non-cellulosic ingredients are alkalized with 1000 parts of an 18 per cent aqueous solution of sodium hydroxide containing 8 per cent sodium chloride based on the weight of dry cellulose for hour at room temperature until the cotton mass is thoroughly saturated with the alkali. The treated cotton is then centrifuged until the weight of the alkali solution remaining is substantially equal to twice the weight of the dry cotton. The centrifuged material is etherified with 15 per cent by weight of ethyleneoxide at 25' C. in a closed container in the presence of at least per cent of sodium chloride based on the weight of dry cellulose. At the end of about 12 hours, the reaction is substantially complete. The excess etherifying agent is withdrawn and the product is washed with hot water until substantially free of alkali and salt. The purified fiber is dried by passing a stream of warm air upwardly therethrough until the fibers are substantially dry to the touch. The product consists of a mass of fibers of textile-making length comprising alkali-soluble cellulose ether, the individual fibers being separable one from another by carding, combing, etc.
The fibers produced by the present invention may be used alone or in admixture with other textile making fibers, such as cotton, flax or wool in the formation of textiles including felts, yarns, threads, cords, fabrics and woven textile structures .of all kinds. The products have a wool-like feel, warmth and appearance.
The textile fibers of the present invention are particularly adapted for use as coalescing fibers. For example, a yarn formed from the. fibers of the invention may be treated with a solvent such as an aqueous alkali solution of sufiicient concentration to superficially, partially or substantially gelatinize the fibers and render them adhesive, whereby the, yarn may then be-squeezed to cause the fibers to coalesce and the alkali neuseparated by carding, combing, and the like.
3. A process for-the production of textile fibers which comprises treating a mass of loose cellulosic fibers of textile-making length with an etherifying agent in the presence of an aqueous solution of an alkali capable of forming an alkali cellulose thereof, continuing the etherification until the cellulose ether fibers produced are soluble in caustic alkali, the etherification betralized with an acid to fix the fibers in the coalesced condition. Likewise the fibers of the present invention may be used as potentially adhesive fibers and thus after being admixed with non-adhesive textile fibers, they may be formed into yarns, threads cords, fabrics and other textiles and the cellulose ether fibers rendered adhesive by a suitable solvent to produce stillened textiles as disclosed and claimed in prior British Patent No. 501,436.
Having described my invention, what I claim and desire to be secured by Letters Patent is:
1. A process for the production of textile fibers which comprises treating a mass or loose cellulosic fibers of textile-making length with an etherifying agent in the presence of an aqueous solution of an alkali capable of forming an cation until the cellulose ether fibers produced are'soluble in caustic alkali, the etherification being carried out in the presence of a quantity of a water-soluble inert salt of an alkali metal suiifllcient to prevent the sticking together of the alkali cellulose thereof, continuing the etherifiing carriedout in the presence of a quantity of a water-soluble inert salt of an alkali metal sufiicient to prevent the sticking together of the fibers, washing the treated fibers with an aqueous solution of a water-soluble inert salt of an alkali metal in sufllcient quantity to prevent gelatinization of the fibers to obtain alkali-soluble cellulose ether fibers of textile-making lengthwhich fibers can be readily separated by carding, combing, and the like.
4. A process for the production of textile fibers which comprises treating a mass of loose cellulosic fibers of textile-making length with an etherifying agent in the presence of an aqueous solution of an alkali capable of forming an alkali cellulose thereof, continuing the etherification until the cellulose ether fibers produced are soluble in caustic alkali, the etherification being carried out in the presence of a quantity of a water-soluble inert salt of an alkali metal sufiicient to prevent the sticking together of the fibers, washing the treated fibers with an aqueous solution of a water-soluble inert salt of an alkali metal in sufiicient quantity to prevent gelatinization of the fibers to obtain alkali-soluble cellulose ether fibers of textile-making length which fibers can be readily separated by carding, comb- -ing,,and the like, and drying the fibers by passing a current of warm air upwardly through the mass of fibers.
5. A process for the production of textile fibers which comprises treating a mass of loose cellulosic fibers of textile-making length with an alkaline swelling agent in the presence of a quantity of water-soluble inert salt of an alkali metal sufiicient to prevent the gelatinization of the fibers,- treating the swollen fibers with an etherifying agent in the presence of an aqueous solution of an alkali capable of forming an alkali cellulose thereof, continuing the etherification until the cellulose ether fibers produced are soluble in caustic alkali, the etherifioation being carried out inthe presenceof a quantity of a alkaline swelling agent in the presence of a water soluble inert salt of an alkali metal and thereafter treating the swollen fibers with an ether-iwater-soluble inert salt or an alkali metal sunlcient to prevent the sticking together or the fibers and washing the fibers with an aqueous solution containing a water-soluble inert salt of an alkali metal and drying the fibers to obtain alkali-soluble cellulose ether fibers of textile-making length which fibers can be readily separated by carding, combing, and the like.
FRANK H. REICHEL.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2289039X | 1938-06-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2289039A true US2289039A (en) | 1942-07-07 |
Family
ID=10903119
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US279040A Expired - Lifetime US2289039A (en) | 1938-06-14 | 1939-06-14 | Process for making textile fibers |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2289039A (en) |
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 |
| US2648635A (en) * | 1948-10-07 | 1953-08-11 | British Celanese | Felted water-soluble cleansing tissue |
| US2729535A (en) * | 1949-06-22 | 1956-01-03 | Balassa Leslie L | Process of making alkali-insoluble cellulose glycolic acid ether fabric |
| US2992880A (en) * | 1955-07-12 | 1961-07-18 | Courtaulds Ltd | Manufacture of threads, fibres, filaments and the like from viscose |
| US3018156A (en) * | 1958-01-06 | 1962-01-23 | American Cyanamid Co | Process of cyanoethylating cellulose in the presence of salts |
| US3218792A (en) * | 1961-10-02 | 1965-11-23 | Courtaulds Ltd | Cellulosic textile material |
-
1939
- 1939-06-14 US US279040A patent/US2289039A/en not_active Expired - Lifetime
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 |
| US2648635A (en) * | 1948-10-07 | 1953-08-11 | British Celanese | Felted water-soluble cleansing tissue |
| US2729535A (en) * | 1949-06-22 | 1956-01-03 | Balassa Leslie L | Process of making alkali-insoluble cellulose glycolic acid ether fabric |
| US2992880A (en) * | 1955-07-12 | 1961-07-18 | Courtaulds Ltd | Manufacture of threads, fibres, filaments and the like from viscose |
| US3018156A (en) * | 1958-01-06 | 1962-01-23 | American Cyanamid Co | Process of cyanoethylating cellulose in the presence of salts |
| US3218792A (en) * | 1961-10-02 | 1965-11-23 | Courtaulds Ltd | Cellulosic textile material |
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