[go: up one dir, main page]

US2067175A - Treatment and manufacture of textile materials - Google Patents

Treatment and manufacture of textile materials Download PDF

Info

Publication number
US2067175A
US2067175A US628181A US62818132A US2067175A US 2067175 A US2067175 A US 2067175A US 628181 A US628181 A US 628181A US 62818132 A US62818132 A US 62818132A US 2067175 A US2067175 A US 2067175A
Authority
US
United States
Prior art keywords
filaments
hydroxy
fibres
cutting
artificial
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
Application number
US628181A
Inventor
Dickie William Alexander
Taylor William Ivan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Celanese Corp
Original Assignee
Celanese Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Celanese Corp filed Critical Celanese Corp
Application granted granted Critical
Publication of US2067175A publication Critical patent/US2067175A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01GPRELIMINARY TREATMENT OF FIBRES, e.g. FOR SPINNING
    • D01G1/00Severing continuous filaments or long fibres, e.g. stapling
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2904Staple length fiber
    • Y10T428/2907Staple length fiber with coating or impregnation

Definitions

  • filaments of artificial material such as cellulose acetate and other cellulose derivatives, celluluosic artificial silks, and to a less degree, natural silk are of a smooth nature, so that staple fibres of such materials are extremely liable to slip and are more difficult to spin into spun yarns than the relatively rough natural fibres such as cotton and wool. Further, spinning of such fibres, particularly in the case of fibres of cellulose acetate or other cellulose derivatives, is rendered difficult by reason of the tendency of the fibres to become electrified during the spinning operation. According to this invention these difiiculties are overcome in a simple manner by a treatment of the filaments during their manufacture into staple fibre.
  • filaments of cellulose acetate or other artificial materials are out into staple lengths while wet following soaking in liquids consisting of or containing a substance selected from the class consisting of compounds having the formula Rl-X-RZ, Where R1 is a hydroxy-or basis amino radicle and R2 is a different radicle' that is a basic amino, acidylamino or acidyl hydroxy radicle and X is an aliphatic residue, and addition products of said compounds with acids.
  • the compounds of this class therefore in all cases contain an aliphatic residue (X) and a salt-forming group (a hydroxy or basic amino radicle) and may also contain an acidylated salt-forming group (an acidylamino or acidyl hydroxy radicle).
  • a salt-forming group a hydroxy or basic amino radicle
  • an acidylated salt-forming group an acidylamino or acidyl hydroxy radicle.
  • Such organic compounds which may be used in accordance with the present invention are the hydroxy alkylamines and/or their derivatives, such as salts, soaps, esters, acid amides, particularly of the higher fatty acids, w-amino-'alkylamides of the higher fatty acids, or dior poly-hydric alcohol derivatives in which some of the hydroxy groups of the alcohols are esterified by fatty acids, particularly the higher fatty acids.
  • the filaments are preferably treated in thick bundles, so that the wetted filaments lie compactly, preferably parallel, or substantially so, it being found that such bundles of wet filaments are both easy to handle and that cutting is facilitated.
  • the application of the hydroxy alkylamine or other'body is eifected in a convenient manner so as to leave a quantity of such material on the fibres being spun which overcomes any difllculty in the several spinning steps due to a tendency of electrification.
  • the hydroxy alkylamines or other bodies may be employed as such, or, where convenient or desired, in the form of solutions or suspension in water or organic solvents in presence or absence of other materials.
  • the bodies or any other liquid in which they are applied should not be capable of exerting any detrimental action on the material of the yarns.
  • hydroxy alkylamines such as mono-, dior tri' ethanolamine, propanolamine, or dioxy-propylamine may be employed, it is, however, preferred that the hydroxy alkaylamines or other bodies employed have a relative high molecular weight.
  • Substituted hydroxy alkylamines such for example as hydroXy-ethyl-aniline may also be used.
  • the hydroxy alkylamines may be employed as such or in the form of their derivatives, such as salts, soaps, esters, and .acid amides and particularly their salts, soaps, esters, or acid amides of higher fatty acids such, for instance, as capric, lauric, myristic, oleic, and stearic acid.
  • the salts or soaps may be the true salts or soaps i. e. containing the molecular equivalents of hydroxy alkylamine and acid or they may contain excess of the same or a different hydroxy alkylamine or of the same or a diiferent acid.
  • partial esters of polyvalent alcohols which may be used according to the invention may be mentioned the higher fatty acid esters of glycols or glycerol, which esters contain free hydroxy groups, for example glycerol mono-oleate, glycerol di-oleate, ethylene glycol mono-oleate and diethylene glycol mono-oleate.
  • esters of other saturated or unsaturated higher fatty acids containing more than 5, e. g. more than 10 carbon atoms, for example stearic, palmitic, or ricinoleic acid.
  • the filament bundles are conveniently in ,the form of hanks and may be treated with the liquid while still on the swift, reel, or drum on which the hank is wound or after removal therefrom.
  • a larger amount of liquid can be taken up, giving the mass a firmness and consistency which is advantageous in handling and cutting while offertioned as examples of solutions that may be ing no inconvenience because of excess liquid.
  • the hanks prior to cutting may be placed while on the swift or other device on which they are wound, or after being removed therefrom, into a vessel containing the liquid to be applied.
  • Solutions of ethanolamines in paraffin oils such for,instance as solutions of triethanolamine in parafiin oils with boiling points of about 110 and upwards, and containing from about 10 to 40% or more of triethanolamine, may be menemployed for the purposes of the invention.
  • the hanks are cut into staple lengths as by means of a guillotine,
  • Drying of the masses of cut fibres may be carried out-either by leaving the fibres on trays, conveyors or the like, or in bags or other containers exposed to the open air or by placing them in suitable chambers, and may be aided,
  • the fibres are brought into a suitable condition for spinning, the hydroxy alkylamine or other body being left on the fibres to an amount dependent on the concentration of the applied liquid and the amount of liquid applied to the filaments.
  • the drying operation referred to above may be preceded by a preliminary centrifuging operation, adapted to reduce the bulk of the liquid on the fibre from, say, which is a suitable proportion for the cutting operation, to, say, 30 to 40% of the weight of the fibre, the concentration of the hydroxy alkylamine or other body in the liquid applied being increased to correspond with the reduced bulk of liquid actually dried ofi the yarn.
  • Roughening media such as silica, barytes, lithopone, and kieselguhr, -or the soluble salts described in U. S. application S. No. 585,381 filed 7th January, 1932, may be applied to the filaments or fibres conjointly with or separately from the hydroxy alkylamines or other bodies to increase the friction between the fibres and so aid the spinning operations.
  • the filaments may be lubricated, e. g. with olive oil, prior to winding or cutting, or instead of or in addition to such lubricating, a lubricant may be added during the treatment with the hydroxy alkylamines or other bodies.
  • liquids containing hydroxy alkylamines .or other bodies may be applied to hanks of filaments by dipping the hanks in solutions.
  • Other methods may, however, be employed in which more accurate control of the amount of applied hydroxy alkylamine or other body may be eiiected.
  • the hanks may be sprayed, or the bodies or liquids containing them may be applied to the filaments in winding operations, e. g. continuously with the production of filaments by the dry or evaporative method,- the hanks or the packages formed being left wet in readiness for the cutting operation.
  • the fibres may be somewhat matted by the wet treatment, but this can be remedied by treatment of the fibres in an apparatus appropriate to their length. For example, in the case of fibres having, a length of say l -2 inches, passage of the dried fibres through an, opener, and subsequently through a scutcher, both of the type used in'the preliminary operations of cotton spinning, readily brings them into a suitable state for the carding operation forming the first of the spinning steps to which such fibres are subjected.
  • the bodies applied to the fibres may be removed from'the yarns immediately after spinning, but in general it is suflicient to allow soaking continuous artificial filaments in a liquid containing a substance selected from the class consisting of compounds having the formula R1X-R2, where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic aminc and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
  • a substance selected from the class consisting of compounds having the formula R1X-R2 where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic aminc and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
  • Process for the production of staple lengths of artificial filaments comprising soaking continuous artificial filaments in a solution' of an ethanolamine in a 'parafiin oil, and then cutting the filaments into staple lengths while they are still wet.
  • Process for the production of staple lengths of artificial filaments comprising soaking continuous artificial filaments in a liquid containing an w-amino-alkylamide of a higher fatty acid, and then cutting the filaments into staple lengths while they are still wet.
  • Process for the production of staple lengths of artificial filaments comprising soaking continuous artificial'filaments in a liquid containing a substance selected from the class consistingpf compounds having the formula R1XR2, where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, forming the continuous filaments into bundles and then cutting the filaing of compounds having the formula Rl-X-Ri, 75
  • R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
  • Process for the production of staple lengths oi artificial filaments comprising soaking continuous artificialfilaments oi cellulose acetate in a liquid containing a substance selected from the class consisting of compounds having the formula RI-XR:, where R1 is a hydroxy group or basic amino radicle and R: is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition prodnets of said-compoimds with acids, and then cutting the filaments into staple lengths while they are stillwet.
  • RI-XR a substance selected from the class consisting of compounds having the formula RI-XR:, where R1 is a hydroxy group or basic amino radicle and R: is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue
  • Process for the production of artificial staple fibres which comprises soaking continuous artificial filaments in a liquid containing a hydroxy alkylamine and then cutting the filaments into staple lengths while they are still wet.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

Patented Jan. 12, 1937 UNITED STATES TREATMENT AND MANUFACTURE OF TEXTILE MATERIALS William Alexander Dickie and William Ivan Taylor, Spondon, near Derby, England, assignors to Celanese Corporation of America, a corporation of Delaware No Drawing. Application August 10, 1932, Serial No. 628,181. In Great Britain August 26, 1931 10 Claims. (01. 18-54) This invention relates to the treatment and manufacture of textile materials and in particular to the manufacture of staple fibre from spun yarns.
It is well known that filaments of artificial material such as cellulose acetate and other cellulose derivatives, celluluosic artificial silks, and to a less degree, natural silk are of a smooth nature, so that staple fibres of such materials are extremely liable to slip and are more difficult to spin into spun yarns than the relatively rough natural fibres such as cotton and wool. Further, spinning of such fibres, particularly in the case of fibres of cellulose acetate or other cellulose derivatives, is rendered difficult by reason of the tendency of the fibres to become electrified during the spinning operation. According to this invention these difiiculties are overcome in a simple manner by a treatment of the filaments during their manufacture into staple fibre.
According to the invention filaments of cellulose acetate or other artificial materials are out into staple lengths while wet following soaking in liquids consisting of or containing a substance selected from the class consisting of compounds having the formula Rl-X-RZ, Where R1 is a hydroxy-or basis amino radicle and R2 is a different radicle' that is a basic amino, acidylamino or acidyl hydroxy radicle and X is an aliphatic residue, and addition products of said compounds with acids. The compounds of this class therefore in all cases contain an aliphatic residue (X) and a salt-forming group (a hydroxy or basic amino radicle) and may also contain an acidylated salt-forming group (an acidylamino or acidyl hydroxy radicle). Such organic compounds which may be used in accordance with the present invention are the hydroxy alkylamines and/or their derivatives, such as salts, soaps, esters, acid amides, particularly of the higher fatty acids, w-amino-'alkylamides of the higher fatty acids, or dior poly-hydric alcohol derivatives in which some of the hydroxy groups of the alcohols are esterified by fatty acids, particularly the higher fatty acids. Mixtures of two or more of such bodies may also be used. The filaments are preferably treated in thick bundles, so that the wetted filaments lie compactly, preferably parallel, or substantially so, it being found that such bundles of wet filaments are both easy to handle and that cutting is facilitated. At the same time, the application of the hydroxy alkylamine or other'body is eifected in a convenient manner so as to leave a quantity of such material on the fibres being spun which overcomes any difllculty in the several spinning steps due to a tendency of electrification.
The hydroxy alkylamines or other bodies may be employed as such, or, where convenient or desired, in the form of solutions or suspension in water or organic solvents in presence or absence of other materials. In fact, it is preferable to apply the bodies in solvents which can be wholly or partially removed from the fibres after cutting to leave the fibres with the required quantity of the applied body and at the degree of dryness necessary for the subsequent spinning operation. The bodies or any other liquid in which they are applied should not be capable of exerting any detrimental action on the material of the yarns.
Though any of the simple hydroxy alkylamines such, for example, as mono-, dior tri' ethanolamine, propanolamine, or dioxy-propylamine may be employed, it is, however, preferred that the hydroxy alkaylamines or other bodies employed have a relative high molecular weight. Substituted hydroxy alkylamines such for example as hydroXy-ethyl-aniline may also be used. The hydroxy alkylamines may be employed as such or in the form of their derivatives, such as salts, soaps, esters, and .acid amides and particularly their salts, soaps, esters, or acid amides of higher fatty acids such, for instance, as capric, lauric, myristic, oleic, and stearic acid. The salts or soaps may be the true salts or soaps i. e. containing the molecular equivalents of hydroxy alkylamine and acid or they may contain excess of the same or a different hydroxy alkylamine or of the same or a diiferent acid.
As examples of partial esters of polyvalent alcohols which may be used according to the invention may be mentioned the higher fatty acid esters of glycols or glycerol, which esters contain free hydroxy groups, for example glycerol mono-oleate, glycerol di-oleate, ethylene glycol mono-oleate and diethylene glycol mono-oleate. Instead of the oleai-es there may be used corresponding esters of other saturated or unsaturated higher fatty acids containing more than 5, e. g. more than 10 carbon atoms, for example stearic, palmitic, or ricinoleic acid.
The filament bundles are conveniently in ,the form of hanks and may be treated with the liquid while still on the swift, reel, or drum on which the hank is wound or after removal therefrom. By arranging the filaments compactly, a larger amount of liquid can be taken up, giving the mass a firmness and consistency which is advantageous in handling and cutting while offertioned as examples of solutions that may be ing no inconvenience because of excess liquid. Thus the hanks prior to cutting may be placed while on the swift or other device on which they are wound, or after being removed therefrom, into a vessel containing the liquid to be applied. Solutions of ethanolamines in paraffin oils, such for,instance as solutions of triethanolamine in parafiin oils with boiling points of about 110 and upwards, and containing from about 10 to 40% or more of triethanolamine, may be menemployed for the purposes of the invention.
'After being allowed to drainuntil they contain the desired amount of liquid, the hanks are cut into staple lengths as by means of a guillotine,
cutting machine.
Drying of the masses of cut fibres may be carried out-either by leaving the fibres on trays, conveyors or the like, or in bags or other containers exposed to the open air or by placing them in suitable chambers, and may be aided,
if desired-by such means as air currents, vacuum, or heat, or combinations thereof for the removal of less volatile constituents of the applied liquid. In this way the fibres are brought into a suitable condition for spinning, the hydroxy alkylamine or other body being left on the fibres to an amount dependent on the concentration of the applied liquid and the amount of liquid applied to the filaments. The drying operation referred to above may be preceded by a preliminary centrifuging operation, adapted to reduce the bulk of the liquid on the fibre from, say, which is a suitable proportion for the cutting operation, to, say, 30 to 40% of the weight of the fibre, the concentration of the hydroxy alkylamine or other body in the liquid applied being increased to correspond with the reduced bulk of liquid actually dried ofi the yarn.
Roughening media such as silica, barytes, lithopone, and kieselguhr, -or the soluble salts described in U. S. application S. No. 585,381 filed 7th January, 1932, may be applied to the filaments or fibres conjointly with or separately from the hydroxy alkylamines or other bodies to increase the friction between the fibres and so aid the spinning operations. The filaments may be lubricated, e. g. with olive oil, prior to winding or cutting, or instead of or in addition to such lubricating, a lubricant may be added during the treatment with the hydroxy alkylamines or other bodies.
As stated above, liquids containing hydroxy alkylamines .or other bodies may be applied to hanks of filaments by dipping the hanks in solutions. Other methods may, however, be employed in which more accurate control of the amount of applied hydroxy alkylamine or other body may be eiiected. For example, the hanks may be sprayed, or the bodies or liquids containing them may be applied to the filaments in winding operations, e. g. continuously with the production of filaments by the dry or evaporative method,- the hanks or the packages formed being left wet in readiness for the cutting operation.
The fibres may be somewhat matted by the wet treatment, but this can be remedied by treatment of the fibres in an apparatus appropriate to their length. For example, in the case of fibres having, a length of say l -2 inches, passage of the dried fibres through an, opener, and subsequently through a scutcher, both of the type used in'the preliminary operations of cotton spinning, readily brings them into a suitable state for the carding operation forming the first of the spinning steps to which such fibres are subjected. v 1
If desired the bodies applied to the fibres may be removed from'the yarns immediately after spinning, but in general it is suflicient to allow soaking continuous artificial filaments in a liquid containing a substance selected from the class consisting of compounds having the formula R1X-R2, where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic aminc and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
2. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial filaments in a liquid containing an ethanolamine, and then cutting the filaments into staple lengths while they are still wet.
3. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial filaments in a solution' of an ethanolamine in a 'parafiin oil, and then cutting the filaments into staple lengths while they are still wet.
4. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial filaments in a solution of triethanolamine in a parafiin oil, and then cutting the filaments into staple lengths while they are still wet. 1
5. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial filaments in a liquid containing an w-amino-alkylamide of a higher fatty acid, and then cutting the filaments into staple lengths while they are still wet.
6. Process for the production of staple lengths of artificial filaments, said process comprising soaking continuous artificial'filaments in a liquid containing a substance selected from the class consistingpf compounds having the formula R1XR2, where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, forming the continuous filaments into bundles and then cutting the filaing of compounds having the formula Rl-X-Ri, 75
where R1 is a hydroxy group or basic amino radicle and R2 is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition products of said compounds with acids, and then cutting the filaments into staple lengths while they are still wet.
8. Process for the production of staple lengths oi artificial filaments, said process comprising soaking continuous artificialfilaments oi cellulose acetate in a liquid containing a substance selected from the class consisting of compounds having the formula RI-XR:, where R1 is a hydroxy group or basic amino radicle and R: is a different radicle selected from the group consisting of basic amino and acidylamino radicles and X is an aliphatic residue, and addition prodnets of said-compoimds with acids, and then cutting the filaments into staple lengths while they are stillwet.
9. Process for the production of artificial staple fibres, which comprises soaking continuous artificial filaments in a liquid containing a hydroxy alkylamine and then cutting the filaments into staple lengths while they are still wet.
1 10. Process for the production of artificial staple fibres, which comprises soaking continuous artificial filaments in a liquid containing a partial acidyl derivative oi a hydroxy alkylaminc, and then cutting the filaments into staple lengths while they are still wet.
WILLIAM Amman mcxm. WILLIAM IVAN rams.
US628181A 1931-08-26 1932-08-10 Treatment and manufacture of textile materials Expired - Lifetime US2067175A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2067175X 1931-08-26

Publications (1)

Publication Number Publication Date
US2067175A true US2067175A (en) 1937-01-12

Family

ID=10897548

Family Applications (1)

Application Number Title Priority Date Filing Date
US628181A Expired - Lifetime US2067175A (en) 1931-08-26 1932-08-10 Treatment and manufacture of textile materials

Country Status (1)

Country Link
US (1) US2067175A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2493031A (en) * 1946-03-29 1950-01-03 Reid John David Prevention of degradation of textile fibers by acids
US2628937A (en) * 1949-01-18 1953-02-17 Courtaulds Ltd Antistatic textile treating composition of triethanolamine-aliphatic carboxylic acidsalts
US2713547A (en) * 1952-08-08 1955-07-19 Edward R Frederick Simulated down filler and method of making the same
US2948103A (en) * 1960-08-09 Process for the manufacture of
US3203821A (en) * 1961-05-25 1965-08-31 Plate Gmbh Dr Flocks for the production of velvet-like or plush-like materials and process for theproduction of such materials by electrostatic means

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2948103A (en) * 1960-08-09 Process for the manufacture of
US2493031A (en) * 1946-03-29 1950-01-03 Reid John David Prevention of degradation of textile fibers by acids
US2628937A (en) * 1949-01-18 1953-02-17 Courtaulds Ltd Antistatic textile treating composition of triethanolamine-aliphatic carboxylic acidsalts
US2713547A (en) * 1952-08-08 1955-07-19 Edward R Frederick Simulated down filler and method of making the same
US3203821A (en) * 1961-05-25 1965-08-31 Plate Gmbh Dr Flocks for the production of velvet-like or plush-like materials and process for theproduction of such materials by electrostatic means

Similar Documents

Publication Publication Date Title
US2461043A (en) Process of conditioning cellulose ester filaments
US2663989A (en) Coated articles and textiles and emulsions for producing them
GB518710A (en) Improvements in synthetic filaments, fibres and articles made therefrom
US2067202A (en) Textile operation
US2297135A (en) Treated textile material
US2666038A (en) Textile-finishing compositions, finished articles, and methods of producing them
US2086544A (en) Textile material and method of preparing the same
US2695270A (en) Oil soluble cationic textile antistatic agent
US2067175A (en) Treatment and manufacture of textile materials
US2079133A (en) Treatment of threads and the like
US2264415A (en) Manufacture of artificial filaments, yarns, and similar materials
US2197930A (en) Method of treating cellulose organic derivative cut staple fibers
US2067174A (en) Manufacture and treatment of textile materials
US2436978A (en) Reinforcing cord and process of manufacture
US2436219A (en) Textile product and process
US2403305A (en) Production of high-twist artificial yarns
US2407105A (en) High tenacity filamentary materials
US2234722A (en) Yarn conditioning process and composition therefor
US2127586A (en) Pile fabric and method of making the same
US2690427A (en) Textile composition
US2319077A (en) Method of producing cellulose derivative crepe yarns
US2682486A (en) Lubrication treatment of textile materials
US2005785A (en) Treatment of filaments, threads, yarns, and the like
GB388426A (en) Improvements in the treatment and manufacture of textile materials
US1725829A (en) Manufacture or treatment of threads of artificial filaments