US2289039A - Process for making textile fibers - Google Patents

Process for making textile fibers Download PDF

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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
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fibers
alkali
cellulose
textile
salt
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Frank H Reichel
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Sylvania Industrial Corp
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Sylvania Industrial Corp
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    • 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 System
    • 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

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.
US279040A 1938-06-14 1939-06-14 Process for making textile fibers Expired - Lifetime US2289039A (en)

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Cited By (6)

* Cited by examiner, † Cited by third party
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

Cited By (6)

* Cited by examiner, † Cited by third party
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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