US2944920A - Process for lubricating and promoting the cohesion of textile fibers - Google Patents

Process for lubricating and promoting the cohesion of textile fibers Download PDF

Info

Publication number
US2944920A
US2944920A US545571A US54557155A US2944920A US 2944920 A US2944920 A US 2944920A US 545571 A US545571 A US 545571A US 54557155 A US54557155 A US 54557155A US 2944920 A US2944920 A US 2944920A
Authority
US
United States
Prior art keywords
fatty acids
polymerized
textile
fibers
acids
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
US545571A
Inventor
William H Shields
Herman T Buckley
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.)
Emery Oleochemicals LLC
Original Assignee
Emery Oleochemicals LLC
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 Emery Oleochemicals LLC filed Critical Emery Oleochemicals LLC
Priority to US545571A priority Critical patent/US2944920A/en
Application granted granted Critical
Publication of US2944920A publication Critical patent/US2944920A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10Treating 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
    • D06M13/184Carboxylic acids; Anhydrides, halides or salts thereof
    • D06M13/192Polycarboxylic acids; Anhydrides, halides or salts thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/507Polyesters
    • D06M15/51Unsaturated polymerisable polyesters

Definitions

  • Textile fabrics are formed by knitting or weaving textile yarns which previously have been formed from the individual textile fibers.
  • the individual fibers may be relatively short in length, such as cotton or wool fibers, or may be continuous as in rayon or the other artificial fibers. in any case many individual fibers make up a yarn and the bundles of fibers must be drawn and twisted to produce a yarn having the proper strength and physical characteristics. During these operations it is desirable to have cohesion between the individual fibers,
  • dimer acid or dilinoleic acid As they have been produced by the dimeriz'ation of linoleic acid or its methyl esters.
  • dimer acid or dilinoleic acid One type of polymerized fatty acids hasbeen generally known as dimer acid or dilinoleic acid as they have been produced by the dimeriz'ation of linoleic acid or its methyl esters.
  • dimer acids from linoleic acids
  • U.S. Patent 2,482,761 One method of producing dimer acids from linoleic acids is disclosed in U.S. Patent 2,482,761.
  • Other methods of bringing about the polymerization of unsaturated fatty acids are disclosed in 'copending applications Ser. Nos. 475,005 and 475,006 which are now Patent Nos. 2,793,219 and 2,793,220 respectively, both issued May 21, 1957.
  • polymerized fatty acids to represent the compounds formed by thepolymerization of two or more molecules of unsaturated acids.
  • polymerized fatty acids regardless of the method of manufacture or raw material source, may be used interchangeably in our process for oiling textiles as the physical properties are the same regardless of the raw materials or the process used in their manufacture.
  • the polymerized acids are tacky or sticky to the touch in which respect the acids resemble molasses.
  • the acids are pressed between the fingers into a film, surprisingly lubricity becomes apparent, and the acids seem more like a heavy lubricating oil than like molasses.
  • the acids by coating the surfaces of textile fibers, promote cohesion thereof advantageously.
  • textile fibre may be cohered and lubricated for practically all textile fabricating operations by a composition comprising from 5 to 50 percent by weight ofpolymerized fatty acids dissolved in an oily diluent.
  • a composition comprising from 5 to 50 percent by weight ofpolymerized fatty acids dissolved in an oily diluent.
  • the polymerized fatty acids by themselves are too viscous to be used alone for any normal or average textile fabricating operation, but are advantageously used when appropriately diluted to reduce viscosity somewhat, though not as far as those skilled in the art would think necessary in the absence of specific instruction or empirical tests.
  • the desired degree of lubricity may be further controlled by selection of a proper diluent.
  • the polymerized fatty acids also have a chemical characteristic which is of very great advantage in textile oil, namely, that their alkali metal soaps are readily water soluble, even more so than the soaps of oleic acid which are widely used in textile processing.
  • textiles which have been treated with the polymerized fatty acid compositions may be much more easily washed or scoured than yarn or fabrics which have'been processed with ordinary oils or soaps or mixtures of them.
  • the washing is preferably conducted in a weak alkaline solution to which ordinary fatty acid soap may be added, if desired.
  • This alkaline solution readily reacts with the polymerized fatty acids, converting them primarily to a highly water soluble thirty-six carbon dibasic fatty acid soaps which are possessed of sufficient emulsifying and detergent properties to usually insure complete removal of the remainder of the dressing from the fiber.
  • the use of ordinary fatty acid soap in the scour may be desirable where added detergency or emulsifying power is needed.
  • the textile fibers may be treated with the polymerized fatty acids either in the form of an admixture with a selected diluent or in admixture With the unpolymerized portion of the fatty acids from which they were derived.
  • the polymerized fatty acids for reasons of economy, are generally produced from the mixtures of fatty acids obtained from naturally occurring 'oils and fats. The saturated acids present in such mixtures are unchanged by the polymerization treatments and a certain proportion of the unsaturated acid remain unpolym'erized.
  • the polymerized fatty acids are generally recovered as residues by distilling oil the unpolymerized monomeric acids.
  • fibers may be processed with the entire mixture of polymerized and unpolymerized acids with or without the addition of further diluents and/or modifying or emulsifying "agents.
  • polymerized acid derivatives In place of the polymerized fatty acids, derivatives of the carboxyl groups of the same may be used in our 'alkanolamines and organic amine soaps. retain the viscous characteristics of the polymerized acids and are hereinafter referred to as polymerized acid derivatives.
  • oily diluents suitable for the purpose are: petroleum oils such as paraffin oils, white mineral oils, and
  • refined lubricating oils vegetable or animal oils such as soyabean oil, teaseed oil, peanut oil, lard oil, fallow oil and sperm oil; liquid fatty acids such as oleic, and the fatty acids derived from soyabean oil, fatty acid esters of monohydric alcohols of from one to eight carbon atoms such as methyl stearate, n-propyl oleate, butyl palmitate and the octylester of coconut oil fatty acids; aliphatic hydrocarbon solvents such as kerosene, Stoddard solvent and mineral spirits and aromatic solvents such as toluene, xylene and solvent naphthas.
  • vegetable or animal oils such as soyabean oil, teaseed oil, peanut oil, lard oil, fallow oil and sperm oil
  • liquid fatty acids such as oleic, and the fatty acids derived from soyabean oil, fatty acid esters of monohydric alcohols of from one
  • oily 'diluents may be used alone or in various admixtures to provide the necessary or desired blending and solvency 'characteristics' and to provide viscosity, lubricity, tack and other characteristics which are necessary or desirable for any particular textile fabricating operation.
  • polymerized fatty acids and the polymerized fatty facid derivatives and the oily dilutents which have been described and identified in the two preceding paragraphs are miscible in all proportions to provide homogeneous Otherwise expressed, the polymerized acids and derivatives are soluble in the oils and the oils are soluble in the acids and derivatives which intersolubility permits the mixing of the ingredients to provide a textile oil having the preselected characteristics which are desired for a given textile fabricating operation.
  • blends of polymerized fatty acids and oily diluents may be rendered miscible with water, if desired, by incorporation of appropriate emulsifying agents, the selection of the agents depending in part upon the characteristics of the oily diluents.
  • an emulsifier of the non-ionic type for rendering the thirty-six carbon dibasic fatty acids dispersible in Among the suitable agents of this type are the sorbitan fatty acid esters, ethoxylated alkyl phenols, ethoxylated fatty acids and the alkanolamine condensates.
  • the process of the invention may be practiced on the individual fibers before carding or spinning or to spun yarns, threads or fabrics by spraying or otherwise coating by means of rollers, wicks and the like.
  • application may be from a volatile solvent applied as indicated above.
  • the process ' may also be practiced by applying the polymerized acid compositions in the form of an emulsion in water in which case emulsions may be formed by incorporating suitable emulsifying agents in the .poly- -merized acid composition or by incorporating alkaline agents such as sodium carbonate, borax or organic alkaline' agents in the Water, emulsification resulting from the soaps of the polymerized acids thus formed.
  • emulsions may be formed by incorporating suitable emulsifying agents in the .poly- -merized acid composition or by incorporating alkaline agents such as sodium carbonate, borax or organic alkaline' agents in the Water, emulsification resulting from the soaps of the polymerized acids thus formed.
  • the petroleum sulfonatcs and monoisopropanolamine aid in stabilizing the emulsion.
  • Sufl'icient emulsion is applied so as to leave 10 percent by weight of the composition on the wool stock.
  • the wool processed in this manner showed less fly loss in carding and produced a more uniform yarn than when processed in the conventional manner.
  • the tow is processed either by spraying or by immersion in an aqueous emulsion of a composition comprising 5 parts of the polymeric ester made by reacting equal molar amounts of polymeric fatty acids and hexaethylene glycol until the acid number of ester is approximately 60, and 95 parts of xylene.
  • the top is sprayed with a composition comprising 20 parts by Weight of the butyl half ester of polymerized fatty acids with parts by weight of propyl oleate.
  • composition comprising 50 parts of the dibutyl ester of polymerized fatty acids and 50 parts of 70 second Saybolt viscosity white mineral oil is applied by means of a wick, roller or immersion of the yarn in composition.
  • the yarn is lubricated by passing over a revolving roller immersed in a composition comprising 10 parts of polymerized fatty acids and'90 parts of lard oil.
  • a process for pretreating organic textile fibers to provide lubricity and promote cohesion during textile fabricating operations comprising applying to the textile fibers a textile dressing comprising a solution of 5% to 50% polymerized fatty acid compound selected from the group consisting of polymerized fatty acids, polymerized esters of fatty acids and monohydric alcohols of up to 8 carbon atoms chain length, and the polymers of polymerized fatty acids and dihydric alcohols of up to 8 carbon atoms chain length, and to 50% of an oily dilutent for the fatty compound said dilutent being selected from the group consisting of animal, vegetable, and mineral oils, liquid fatty acids, and the liquid esters of fattyacids.

Description

United States Patent 50?? PROCESS FOR LUBRICATING AND PROMOTING THE COHESION F TEXTILE FIBERS William H. Shields, Wyoming, and i ierman T. Buckley, Cincinnati, Ohio, assignors to Emery Industries, Inn, Cincinnati, Ohio, a corporation of Ohio No Drawing. Filed Nov. 7, 1955, Sen-No. 545,571
'2 Claims. cl. tir -129s This invention relates to a process for lubricating and promiting the cohesion of textile fibers, natural or synthetic, such as wool, rayon or nylon, which facilitates the operations which are performedupon them in the various textile fabricating processes such as carding, drawing, spinning, winding and the like. This application is a continuation in part of our co-pending application, Serial No. 246,330, filed on September 12, 1951, for Dressing for Textile Fibers.
Textile fabrics are formed by knitting or weaving textile yarns which previously have been formed from the individual textile fibers. The individual fibers may be relatively short in length, such as cotton or wool fibers, or may be continuous as in rayon or the other artificial fibers. in any case many individual fibers make up a yarn and the bundles of fibers must be drawn and twisted to produce a yarn having the proper strength and physical characteristics. During these operations it is desirable to have cohesion between the individual fibers,
in the case of the shorter fibers to obtain strength and in sary that lubrication be provided between the fibers and the parts of the machinery with which they come in contact.
It is the purpose of this invention to provide a proccss which promotes cohesion between the individual fibers and at the same time lubricates the fibers. Our process may be adapted to various types of textile operations by the use of appropriate treating compositions, as will later be described, and provides many advantages such as the reduction of losses in carding, reduction of dropped ends during roving and spinning operations, increase in average tensile strength of the yarn produced, in addition to lubricating the fibers.
These benefits are achieved by the process in which polymerized fatty acids compounded with an appropriate oily diluent or viscosity reducer are applied to the fibers prior. to the steps of mechanical treatment.
One type of polymerized fatty acids hasbeen generally known as dimer acid or dilinoleic acid as they have been produced by the dimeriz'ation of linoleic acid or its methyl esters. One method of producing dimer acids from linoleic acids is disclosed in U.S. Patent 2,482,761. Other methods of bringing about the polymerization of unsaturated fatty acids are disclosed in 'copending applications Ser. Nos. 475,005 and 475,006 which are now Patent Nos. 2,793,219 and 2,793,220 respectively, both issued May 21, 1957. t
The products of all of these methods of manufacture are primarily thirty-six carbon dibasic acids. They are very viscous liquids which upon superficial inspection seem to be like heavy molasses or heavy lubricating oil. Even though substantially identical inpertinent physical properties it is not probable that the chemicalst'ructures of the acids made by difie'rent processes are identical as the acids difier in iodinevaliie, which depends both upon 2,944,920 Patented July 12, 1960 the nature of the starting materials and the nature of the polymerization process employed.
We prefer, therefore, to use the term polymerized fatty acids to represent the compounds formed by thepolymerization of two or more molecules of unsaturated acids. We have also found that all polymerized acids, regardless of the method of manufacture or raw material source, may be used interchangeably in our process for oiling textiles as the physical properties are the same regardless of the raw materials or the process used in their manufacture. V
The polymerized acids are tacky or sticky to the touch in which respect the acids resemble molasses. On the other hand, if the acids are pressed between the fingers into a film, surprisingly lubricity becomes apparent, and the acids seem more like a heavy lubricating oil than like molasses. The acids, by coating the surfaces of textile fibers, promote cohesion thereof advantageously.
We have discovered and deter-mined that textile fibre may be cohered and lubricated for practically all textile fabricating operations by a composition comprising from 5 to 50 percent by weight ofpolymerized fatty acids dissolved in an oily diluent. In general, we utilize compositions of greater viscosity than the textile 'oils which have been most commonly used for the particular operation in question. In other words, the polymerized fatty acids by themselves are too viscous to be used alone for any normal or average textile fabricating operation, but are advantageously used when appropriately diluted to reduce viscosity somewhat, though not as far as those skilled in the art would think necessary in the absence of specific instruction or empirical tests. 7 The desired degree of lubricity may be further controlled by selection of a proper diluent.
The polymerized fatty acids also have a chemical characteristic which is of very great advantage in textile oil, namely, that their alkali metal soaps are readily water soluble, even more so than the soaps of oleic acid which are widely used in textile processing. On this account, textiles which have been treated with the polymerized fatty acid compositions may be much more easily washed or scoured than yarn or fabrics which have'been processed with ordinary oils or soaps or mixtures of them. The washing is preferably conducted in a weak alkaline solution to which ordinary fatty acid soap may be added, if desired. This alkaline solution readily reacts with the polymerized fatty acids, converting them primarily to a highly water soluble thirty-six carbon dibasic fatty acid soaps which are possessed of sufficient emulsifying and detergent properties to usually insure complete removal of the remainder of the dressing from the fiber. The use of ordinary fatty acid soap in the scour may be desirable where added detergency or emulsifying power is needed.
The textile fibers may be treated with the polymerized fatty acids either in the form of an admixture with a selected diluent or in admixture With the unpolymerized portion of the fatty acids from which they were derived. The polymerized fatty acids, for reasons of economy, are generally produced from the mixtures of fatty acids obtained from naturally occurring 'oils and fats. The saturated acids present in such mixtures are unchanged by the polymerization treatments and a certain proportion of the unsaturated acid remain unpolym'erized. The polymerized fatty acids are generally recovered as residues by distilling oil the unpolymerized monomeric acids. However, for the purposes of this invention fibers may be processed with the entire mixture of polymerized and unpolymerized acids with or without the addition of further diluents and/or modifying or emulsifying "agents.
In place of the polymerized fatty acids, derivatives of the carboxyl groups of the same may be used in our 'alkanolamines and organic amine soaps. retain the viscous characteristics of the polymerized acids and are hereinafter referred to as polymerized acid derivatives.
- blends.
- water.
The oily diluents suitable for the purpose are: petroleum oils such as paraffin oils, white mineral oils, and
refined lubricating oils; vegetable or animal oils such as soyabean oil, teaseed oil, peanut oil, lard oil, fallow oil and sperm oil; liquid fatty acids such as oleic, and the fatty acids derived from soyabean oil, fatty acid esters of monohydric alcohols of from one to eight carbon atoms such as methyl stearate, n-propyl oleate, butyl palmitate and the octylester of coconut oil fatty acids; aliphatic hydrocarbon solvents such as kerosene, Stoddard solvent and mineral spirits and aromatic solvents such as toluene, xylene and solvent naphthas. These oily 'diluents may be used alone or in various admixtures to provide the necessary or desired blending and solvency 'characteristics' and to provide viscosity, lubricity, tack and other characteristics which are necessary or desirable for any particular textile fabricating operation.
The polymerized fatty acids and the polymerized fatty facid derivatives and the oily dilutents which have been described and identified in the two preceding paragraphs are miscible in all proportions to provide homogeneous Otherwise expressed, the polymerized acids and derivatives are soluble in the oils and the oils are soluble in the acids and derivatives which intersolubility permits the mixing of the ingredients to provide a textile oil having the preselected characteristics which are desired for a given textile fabricating operation.
These blends of polymerized fatty acids and oily diluents may be rendered miscible with water, if desired, by incorporation of appropriate emulsifying agents, the selection of the agents depending in part upon the characteristics of the oily diluents. In general, it is desirable to use an emulsifier of the non-ionic type for rendering the thirty-six carbon dibasic fatty acids dispersible in Among the suitable agents of this type are the sorbitan fatty acid esters, ethoxylated alkyl phenols, ethoxylated fatty acids and the alkanolamine condensates.
The process of the invention may be practiced on the individual fibers before carding or spinning or to spun yarns, threads or fabrics by spraying or otherwise coating by means of rollers, wicks and the like. In certain instances, application may be from a volatile solvent applied as indicated above.
The process 'may also be practiced by applying the polymerized acid compositions in the form of an emulsion in water in which case emulsions may be formed by incorporating suitable emulsifying agents in the .poly- -merized acid composition or by incorporating alkaline agents such as sodium carbonate, borax or organic alkaline' agents in the Water, emulsification resulting from the soaps of the polymerized acids thus formed.
Examples 7 I. Raw wool, prior to carding, is treated withan emulmonoisopropanolamine.
the petroleum sulfonatcs and monoisopropanolamine aid in stabilizing the emulsion.
Sufl'icient emulsion is applied so as to leave 10 percent by weight of the composition on the wool stock. The wool processed in this manner showed less fly loss in carding and produced a more uniform yarn than when processed in the conventional manner.
II. In the conversion of viscose rayon tow into staple fibers, the tow is processed either by spraying or by immersion in an aqueous emulsion of a composition comprising 5 parts of the polymeric ester made by reacting equal molar amounts of polymeric fatty acids and hexaethylene glycol until the acid number of ester is approximately 60, and 95 parts of xylene.
III. In the treatment of worsted fibers, the top is sprayed with a composition comprising 20 parts by Weight of the butyl half ester of polymerized fatty acids with parts by weight of propyl oleate.
IV. For the overoiling of sized nylon hosiery yarn,
a composition comprising 50 parts of the dibutyl ester of polymerized fatty acids and 50 parts of 70 second Saybolt viscosity white mineral oil is applied by means of a wick, roller or immersion of the yarn in composition.
V. For the coning of cellulose acetate yarn, the yarn is lubricated by passing over a revolving roller immersed in a composition comprising 10 parts of polymerized fatty acids and'90 parts of lard oil.
The improvements in processing which result from the use of our process are believed to be due to the fact that the polymerized fatty acids impart an unusual and characteristic tackiness to the individual fibers themselves, which tackiness promotes cohesion between the fibers, but at the same time does not decrease or impair the lubricity which is otherwise requisite to avoid friction under the conditions of operation. Additionally, our process applies compositions which are very readily removed from fibers and do not interfere with subsequent bleaching or dyeing operations. Moreover, since our process employs compositions which are relatively stable and standard chemicals, any variation of our process which has been found to be particularly suitable for any particular textile fabricating operation may be reproduced with substantial exactitude,
It is to be understood that all proportions of materials which are disclosed herein are given by weight.
Having described our invention, we claim:
1. A process for pretreating organic textile fibers to provide lubricity and promote cohesion during textile fabricating operations said process comprising applying to the textile fibers a textile dressing comprising a solution of 5% to 50% polymerized fatty acid compound selected from the group consisting of polymerized fatty acids, polymerized esters of fatty acids and monohydric alcohols of up to 8 carbon atoms chain length, and the polymers of polymerized fatty acids and dihydric alcohols of up to 8 carbon atoms chain length, and to 50% of an oily dilutent for the fatty compound said dilutent being selected from the group consisting of animal, vegetable, and mineral oils, liquid fatty acids, and the liquid esters of fattyacids.
2. The process of claim 1 in which the textile dressing has been rendered self-emulsifying in water by incorporation of a suitable emulsifying agent therein.
References Cited in the file of this patent .UNITED STATES PATENTS 2,348,552 Little May 9, 1944 2,400,393 De Groote May 14, 1946 2,558,494 Meet-burg June 26, i 2,631,979 McDermott Mar. 17, 1953 2,671,744 Biefeld et al. Mar. 9, 1954 2,682,486 Humphreys June 29, 1954 2,690,426 Jefferson et al. Sept. 28, 1954 2,706,713 Sproule et a1 Apr. 19, 1955 2,740,759 Maeder et al. Apr. 3, 1956 2,812,342 Peters Nov.- 5, 1957

Claims (1)

1. A PROCESS FOR PRETREATING ORGANIC TEXTILE FIBERS TO PROVIDE LUBRICITY AND PROMOTE COHESION DURING TEXTILE FABRICATING OPERATIONS SAID PROCESS COMPRISING APPLYING TO THE TEXTILE FIBERS A TEXTILE DRESSING COMPRISING A SOLUTION OF 5% TO 50% POLYMERIZED FATTY ACID COMPOUND SELECTED FROM THE GROUP CONSISTING OF POLYMERIZED FATTY ACIDS, POLYMERIZED ESTERS OF FATTY ACIDS AND MONOHYDRIC ALCOHOLS OF UP TO 8 CARBON ATOMS CHAIN LENGTH, AND THE POLYMERS OF POLYMERIZED FATTY ACIDS AND DIHYDRIC ALCOHOLS OF UP TO 8 CARBON ATOMS CHAIN LENGTH AND 95% TO 50% OF AN OILY DILUTENT FOR THE FATTY COMPOUND SAID DILUTENT BEING SELECTED FROM THE GROUP CONSISTING OF ANIMAL, VEGETABLE, AND MINERAL OILS, LIQUID FATTY ACIDS, AND THE LIQUID ESTERS OF FATTY ACIDS.
US545571A 1955-11-07 1955-11-07 Process for lubricating and promoting the cohesion of textile fibers Expired - Lifetime US2944920A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US545571A US2944920A (en) 1955-11-07 1955-11-07 Process for lubricating and promoting the cohesion of textile fibers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US545571A US2944920A (en) 1955-11-07 1955-11-07 Process for lubricating and promoting the cohesion of textile fibers

Publications (1)

Publication Number Publication Date
US2944920A true US2944920A (en) 1960-07-12

Family

ID=24176753

Family Applications (1)

Application Number Title Priority Date Filing Date
US545571A Expired - Lifetime US2944920A (en) 1955-11-07 1955-11-07 Process for lubricating and promoting the cohesion of textile fibers

Country Status (1)

Country Link
US (1) US2944920A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3160511A (en) * 1960-06-09 1964-12-08 Monsanto Co Treatment of polyamide filaments
US3197333A (en) * 1960-08-30 1965-07-27 Berol Aktiebolag Processes of treating textile fibres before forming the same into a yarn
DE1215103B (en) * 1963-01-11 1966-04-28 Th Boehme K G Chem Fab Dr Process for spin finishing synthetic fibers
US3279943A (en) * 1960-06-09 1966-10-18 Monsanto Co Polyamide filamentary yarn
US4218498A (en) * 1974-08-21 1980-08-19 Imperial Chemical Industries Limited Process for preparing a polymeric film

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2348552A (en) * 1941-03-27 1944-05-09 Hercules Powder Co Ltd Textile fiber and method of producing
US2400393A (en) * 1944-08-16 1946-05-14 Petrolite Corp New composition of matter
US2558494A (en) * 1951-06-26 X tm x t
US2631979A (en) * 1950-08-30 1953-03-17 Standard Oil Dev Co Rust inhibiting composition
US2671744A (en) * 1951-02-09 1954-03-09 Owens Corning Fiberglass Corp Sized strands and method of making same
US2682486A (en) * 1948-12-17 1954-06-29 Celanese Corp Lubrication treatment of textile materials
US2690426A (en) * 1950-03-07 1954-09-28 Atlas Powder Co Lubricating compositions
US2706713A (en) * 1952-06-13 1955-04-19 Exxon Research Engineering Co Textile oil
US2740759A (en) * 1951-11-13 1956-04-03 Ciba Ltd Preparation for treating textile fibers and yarns
US2812342A (en) * 1955-04-29 1957-11-05 Emery Industries Inc Hydrogenation of structurally modified acids and products produced thereby

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2558494A (en) * 1951-06-26 X tm x t
US2348552A (en) * 1941-03-27 1944-05-09 Hercules Powder Co Ltd Textile fiber and method of producing
US2400393A (en) * 1944-08-16 1946-05-14 Petrolite Corp New composition of matter
US2682486A (en) * 1948-12-17 1954-06-29 Celanese Corp Lubrication treatment of textile materials
US2690426A (en) * 1950-03-07 1954-09-28 Atlas Powder Co Lubricating compositions
US2631979A (en) * 1950-08-30 1953-03-17 Standard Oil Dev Co Rust inhibiting composition
US2671744A (en) * 1951-02-09 1954-03-09 Owens Corning Fiberglass Corp Sized strands and method of making same
US2740759A (en) * 1951-11-13 1956-04-03 Ciba Ltd Preparation for treating textile fibers and yarns
US2706713A (en) * 1952-06-13 1955-04-19 Exxon Research Engineering Co Textile oil
US2812342A (en) * 1955-04-29 1957-11-05 Emery Industries Inc Hydrogenation of structurally modified acids and products produced thereby

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3160511A (en) * 1960-06-09 1964-12-08 Monsanto Co Treatment of polyamide filaments
US3279943A (en) * 1960-06-09 1966-10-18 Monsanto Co Polyamide filamentary yarn
US3197333A (en) * 1960-08-30 1965-07-27 Berol Aktiebolag Processes of treating textile fibres before forming the same into a yarn
DE1215103B (en) * 1963-01-11 1966-04-28 Th Boehme K G Chem Fab Dr Process for spin finishing synthetic fibers
US4218498A (en) * 1974-08-21 1980-08-19 Imperial Chemical Industries Limited Process for preparing a polymeric film

Similar Documents

Publication Publication Date Title
US4106901A (en) Emulsifier-solvent scour composition and method of treating textiles therewith
US4169062A (en) Random copolymers of polyoxyethylene polyoxypropylene glycol monoester, process of making the same and textile fiber containing the same
US2664409A (en) Textile treating composition and method
US3639235A (en) Antistatic carding lubricant
US2565403A (en) Textile oils
US2418752A (en) Yarn having the twist set therein with an unctuous solid
US2944920A (en) Process for lubricating and promoting the cohesion of textile fibers
US2976186A (en) Treated textile fiber
US2385423A (en) Treatment of textile materials
US2496631A (en) Wool treatment
US1985687A (en) Oiling and dressing fibers
US2857330A (en) Anhydrous textile finishes
US2182323A (en) Treatment of textile materials
US2865855A (en) Textile treating composition
US2407105A (en) High tenacity filamentary materials
JPS597828B2 (en) Smoothing agent composition for synthetic fibers with antistatic effect
US2406408A (en) Treatment of textile materials
US2093863A (en) Textile oils
US2684311A (en) Process for lubricating regenerated cellulose yarns
US2176402A (en) Treatment of artificial silk
US3470095A (en) Aqueous textile treating emulsion
US2002885A (en) Textile fiber spraying oils
US3197333A (en) Processes of treating textile fibres before forming the same into a yarn
US2328600A (en) Treatment of textile materials
US2245412A (en) Yarn treating composition and process