US2944920A - Process for lubricating and promoting the cohesion of textile fibers - Google Patents
Process for lubricating and promoting the cohesion of textile fibers Download PDFInfo
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- 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
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- fatty acids
- polymerized
- textile
- fibers
- acids
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- 239000004753 textile Substances 0.000 title claims description 32
- 239000000835 fiber Substances 0.000 title claims description 31
- 238000000034 method Methods 0.000 title claims description 24
- 230000001050 lubricating effect Effects 0.000 title description 4
- 230000001737 promoting effect Effects 0.000 title description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 42
- 239000000194 fatty acid Substances 0.000 claims description 42
- 229930195729 fatty acid Natural products 0.000 claims description 42
- 150000004665 fatty acids Chemical class 0.000 claims description 38
- -1 FATTY ACID COMPOUND Chemical class 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 5
- 239000002480 mineral oil Substances 0.000 claims description 4
- 239000010775 animal oil Substances 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000008158 vegetable oil Substances 0.000 claims description 3
- 235000013311 vegetables Nutrition 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 2
- 239000002253 acid Substances 0.000 description 24
- 239000000203 mixture Substances 0.000 description 20
- 150000007513 acids Chemical class 0.000 description 18
- 239000003921 oil Substances 0.000 description 13
- 235000019198 oils Nutrition 0.000 description 13
- 239000003085 diluting agent Substances 0.000 description 9
- 239000000344 soap Substances 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 150000002148 esters Chemical class 0.000 description 6
- 238000009960 carding Methods 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 210000002268 wool Anatomy 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 230000001804 emulsifying effect Effects 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 235000013379 molasses Nutrition 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 244000068988 Glycine max Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
- HPEUJPJOZXNMSJ-UHFFFAOYSA-N Methyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC HPEUJPJOZXNMSJ-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- GLYJVQDYLFAUFC-UHFFFAOYSA-N butyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCC GLYJVQDYLFAUFC-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000010699 lard oil Substances 0.000 description 2
- 235000020778 linoleic acid Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- FDVCQFAKOKLXGE-UHFFFAOYSA-N 216978-79-9 Chemical compound C1CC(C)(C)C2=CC(C=O)=CC3=C2N1CCC3(C)C FDVCQFAKOKLXGE-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010495 camellia oil Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- VJZWIFWPGRIJSN-XRHABHTOSA-N dilinoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O.CCCCC\C=C/C\C=C/CCCCCCCC(O)=O VJZWIFWPGRIJSN-XRHABHTOSA-N 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- CAMHHLOGFDZBBG-UHFFFAOYSA-N epoxidized methyl oleate Natural products CCCCCCCCC1OC1CCCCCCCC(=O)OC CAMHHLOGFDZBBG-UHFFFAOYSA-N 0.000 description 1
- OVBPIULPVIDEAO-LBPRGKRZSA-N folic acid Chemical class C=1N=C2NC(N)=NC(=O)C2=NC=1CNC1=CC=C(C(=O)N[C@@H](CCC(O)=O)C(O)=O)C=C1 OVBPIULPVIDEAO-LBPRGKRZSA-N 0.000 description 1
- IIRDTKBZINWQAW-UHFFFAOYSA-N hexaethylene glycol Chemical compound OCCOCCOCCOCCOCCOCCO IIRDTKBZINWQAW-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—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
- D06M13/192—Polycarboxylic 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
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/507—Polyesters
- D06M15/51—Unsaturated 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.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
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.
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)
| 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 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| 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 |
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Patent Citations (10)
| 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)
| 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 |
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