US2853451A - Lubricating agents - Google Patents
Lubricating agents Download PDFInfo
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- US2853451A US2853451A US492308A US49230855A US2853451A US 2853451 A US2853451 A US 2853451A US 492308 A US492308 A US 492308A US 49230855 A US49230855 A US 49230855A US 2853451 A US2853451 A US 2853451A
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/244—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus
- D06M13/282—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing sulfur or phosphorus with compounds containing phosphorus
- D06M13/292—Mono-, di- or triesters of phosphoric or phosphorous acids; Salts thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/02—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M7/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made of other substances with subsequent freeing of the treated goods from the treating medium, e.g. swelling, e.g. polyolefins
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/14—Synthetic waxes, e.g. polythene waxes
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/17—Fisher Tropsch reaction products
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/043—Ammonium or amine salts thereof
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/46—Textile oils
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/015—Dispersions of solid lubricants
- C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/40—Reduced friction resistance, lubricant properties; Sizing compositions
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- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2965—Cellulosic
Definitions
- Another .object of this invention is the provision of novel and highly eifective lubricating agents for yarns of cellulose acetate or other organic derivative of cellulose.
- the lubricating agents of this invention contain a mixture of eicosane and an amine salt of an acid phosphate of-a higher fatty alcohol. 'Advantageously, they also contain an amine salt of a higher fatty acid.
- the lubricating compositions of this invention are preferably prepared by mixing the eicosane in molten condition with an ester-forming phosphorus acid derivative, such as phosphorus pentoxide, and adding to the mixture a higher fatty alcohol, in amount suflicient to form an acidic phosphate of said alcohol, together with a higher fatty acid, while maintaining the said mixture at an elevated temperature. Thereafter an amine is added to the mixture to form the salts of the acidic phosphate and of the higher fatty acid.
- an ester-forming phosphorus acid derivative such as phosphorus pentoxide
- the amine used in the productionof the lubricating compositions preferably contains a hydroxyl group.
- suitable tertiary amines of this type are dibutylethanolamine, triethanolamine, diethylethanolamine and triisopropanolamine.
- Amines containing no hydroxyl substituents e. g. N,N-diethylcyclohexylamine, may be used, if desired.
- secondary amines such as diethylamine or diethanolamine may be employed instead.
- the alcohol used to form the acidic phosphate ester advantageously contains at least12 carbon atoms, preferably about 14 to 20 carbon atoms. Mixtures of alcohols for example, blends of homologous or isomeric alcohols, may be employed if desired. Examples of suitable alcohols are octadecyl (stearyl), octadecenyl (oleyl), and hexadecyl (cetyl), or mixtures of the same. Examples of ester-forming phosphorus acid derivatives suitable for reaction with the alcohol are phosphorus pentoxide, which is preferred, and phosphorus tetroxide.
- Phosphorus pentachloride may also be used but is somewhat less desirable since it liberates corrosive hydrochloric acid during the esterificationreaction.
- the relative amounts of the ester-forming phosphorus acid derivative and the higher fatty alcohol may be such that the resulting ester contains about 1 to 2, preferably 1.3 to 1.6, higher fatty alcohol radicals per phosphorus atom.
- the higher fatty acid used in the production of the higher fatty acid about 10 to 40%, preferably about 20 to 25%. If desired, there may be employed a slight excess of amine over that necessary to form the salts of the acidic constituents. For best results the amount of amine is such that the pH of an aqueous dispersion of the composition, of 20 to 30% concentration, is about 7.5 to 8.5.
- the lubricating compositions of this invention maybe applied to the filamentary material in any desired manner.
- the composition may be applied as a molten mixture, as a solution in a volatile solvent, or, most desirably, as a dispersion in water.
- the amine salts of the phosphate esters and fatty acids act, in part, as emulsifying agents so that the composition disperses easily in water.
- Suitable concentrations of the composition in Water are, for example, 5 to 35%, preferably 20 to 30% by Weight.
- an additional emulsifying agent may be incorporated into the mixture to improve the stability of the dispersion. Examples of such emulsifying agents are those polyethylene oxide derivatives known as Igepal CA-630, Brij 30, Lipal 30W, BS- and Sp'an 85.
- the lubricating compositions of this invention are particularly useful for use on filamentary materials of cellulose acetate of about 53 to 55% acetyl value, calculated as combined acetic acid. They may also be applied to filamentary materials of other organic derivatives of cellulose, e. g. other cellulose esters, such as cellulose triacetate, cellulose propionate, cellulose butyrate, cellulose acetate-propionate and cellulose acetate-butyrate, or cellulose ethers, such as ethyl cellulose or benzyl cellulose. They are also useful for the lubrication of other filamentary.
- compositions may be applied to continuous filaments as they emerge, in the form of a yarn, from the spinning cabinet or metier in which they are formed. Similarly, they may be applied to tows, or relatively thick bundles, of continuous filaments before said bundles are severed into staple fibers of the desired length, or they may be applied to the staple fibers themselves at any desired stage in the processing of said staple fibers.
- the amount of the composition is about 1 to 4%, based on the weight of said filamentary material.
- lubricating compositions of this invention greatly reduces the drag occurring when filamentary materials are passed over guide surfaces.
- their application to cellulose acetate yarns has made it possible to knit such yarns in a highly successful manner on circular knitting machines under such drastic conditions as had previously precluded the use of cellulose acetate yarns carrying the conventional lubricating agents.
- the lubricating compositions of this invention show practically no change in characteristics on aging, either in the presence or absence of small amounts of water, have practically no tendency to corrode black iron, have excellent antistatic properties, improve the flex abrasion characteristics of the filamentary material, and may be very easily removed from the filamentary material by scouring in water.
- Example I 33.6 parts of the crystalline product consisting predominantly of n-eicosane, having a melting point of 96.5 F. and having 10% and 90% boiling points of 383 F. and 410 F., respectively, measured at 10 mm. Hg absolute, sold under the name Eicosane by Atlantic Refining Company, are melted and 4.3 parts of finely divided phosphorus pentoxide are added thereto and mixed for 5 minutes to form a slurry. The temperature of the slurry is adjusted to 60 C. and then 24.4 parts of oleyl alcohol and 13.0 parts of oleic acid are added quickly. The ensuing reaction causes the temperature to rise. Then the mixture is heated further and maintained at a temperature of 80 C. for 30 minutes while it is stirred vigorously.
- Example II Example II is repeated except that the Igepal CA-630 is omitted. The resulting mixture is applied in molten condition, at 35 to 40 C., to the yarn.
- the lubricating efiect is substantially the same as in Example 1.
- Example III Example III is repeated except that 35 parts of eicosane are employed; 24.5 parts of stearyl alcohol and 13.2 parts of stearic acid are substituted for the oleyl alcohol and oleic acid, respectively; 18 parts of triethanolamine are substituted for the dibutylethanolamine; and the stearic acid is added after the stearyl alcohol has been reacted in the mixture for the 30 minute period.
- the product is a hard wax. This wax is emulsified by first mixing it thoroughly with twice its weight of water having a temperature of 80 C., to form a paste, cooling the paste and adding the desired amount of cold Water. The resulting composition has substantially the same lubricating properties as that of Example I.
- Example I V Thirty parts of the triethanolamine ester of stearic acid and thirty parts of the triethanolamine salt of stearyl phosphate are mixed in forty parts of molten eicosane 4 until a homogeneous mixture results. On cooling, a hard wax results. This wax is .emulsified by first mixing it thoroughly with twice its weight of water having a temperature of 80 C., to form a paste, cooling the paste and adding the desired amount of cold water. The product has good lubricating properties.
- a lubricating composition for filamentary materials comprising about 20 to 45 parts by weight ,of n-eicosane and about 25 to 45 parts by weight of an amine salt of an acid phosphate of a higher fatty alcohol.
- a lubricating composition for filamentary materials comprising about 20 to 45% of n-eicosane, about 25 ,to 45 of an amine sale of an acid phosphate of a higher fatty alcohol, and about 10 to 40% of an amine salt of a higher fatty acid.
- a lubricating composition for filamentary materials comprising about 20 to 45 parts by weight of n-eicosane, about'25 to 45 parts by Weight of an amine salt of an acid phosphate of a higher fatty alcohol, and about 10 to 40 parts by weight of an amine salt of a higher fatty acid, dispersed to a concentration of about 20 to in an aqueous medium in the presence of a non-ionic emulsifying agent.
- Cellulose acetate filamentary material carrying a coating of the lubricating composition of claim 3 in which the tertiary amine in each case contains an alcoholic hydroxyl group.
- a lubricating composition for filamentary materials comprising about 30 to of n-eicosane, about 3.0 to of a tertiary amine salt of an acid phosphate of oleyl alcohol, and about 20 to 30% of a tertiary amine salt of oleic acid, said tertiary amine in each case containing an alcoholic hydroxyl group.
- a lubricating composition for filamentary materials comprising about 35 to of n-eicosane, about 25 to 35% of a tertiary amine salt of an acid phosphate of stearyl alcohol, and about 25 to 35% of a tertiary amine salt of stearic acid, said tertiary amine in each case containing an alcoholic hydroxyl group.
- Process for the production of lubricating compositions which comprises forming a mixture of about 20 to 45 parts by weight of molten n-eicosane and an esterforming phosphorus acid derivative, adding to the mixture a higher fatty alcohol, in amount sufficient to react with said phosphorus acid derivative to form an acidic phosphate of said alcohol, while maintaining said mixture at an elevated esterification temperature, and thereafter adding an amine to the resulting mixture to form an amine salt of said acidic phosphate, said phosphorus acid derivative, higher fatty alcohol and amine being added in amount sufiicient to form about 25 to 45 parts by weight of the amine salt of said acidic phosphate.
- Process for the production of lubricating compositions which comprises forming a mixture of molten n-eicosane and an ester-forming phosphorus acid derivative, adding to the mixture a higher fatty alcohol, in amount sufiicient to react with said phosphorus acid derivative to form an acidic phosphate of said alcohol, together with a higher fatty acid, while maintaining said mixture atan elevated, esterification temperature, adding an amine to the resulting mixture to form amine salts of said acidic phosphate and said higher fatty acid, and thereafter emulsifying the mixture in Water.
- Process for the production of lubricating compositions which comprises forming a mixture of about 20 to 45 parts by Weight of molten n-eicosane and an esterforming phosphorus acid derivative, adding to the mixture a higher fatty alcohol, in amount sufficient to react with said phosphorus acid derivative to form an acidic phosphate of said alcohol, together with a higher fatty acid, while maintaining said mixture at an elevated esteri- 'fication temperature, adding an amine to the resulting mixture to form amine salts of said acidic phosphate and said higher fatty acid, said phosphorus acid derivative, higher fatty alcohol, higher fatty acid and amine being added in amount sufiicient to form about to 45 parts by Weight of the amine salt of said acidic phosphate and about 10 to 40 parts by Weight of the amine salt of said higher fatty acid, and thereafter emulsifying the mixture in water to a concentration of about 20 to References Cited in the file of this patent UNITED STATES PATENTS 1,914,331 Nues,
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Description
United States Patent 6 LUBRICATING AGENTS Fred Fortess, Summit, N. J., Conrad Hohing, Jr., Cumberland, Md., and Charles E. Kip, Montclair, N. J., assignors to Celanese Corporation of America, New York, N. Y., a corporation of Delaware No Drawing. Application March 4, 1955 Serial No. 492,308
I 15 Claims. (Cl. zsz-as guide surfaces, is an important factor in the efficiency of the knitting process. In fact, in some types of circular knitting machines this factor causes the articles produced thereby to show runs or holes when the drag is too great.
It is an object of this invention to provide new and improved lubricating agents for application to filamentary materials, which agents will act to decrease greatly the drag of said filamentary materials and will enable said materials to be .knitted on circular knitting machines at high speeds to produce fabrics of excellent quality.
Another .object of this invention is the provision of novel and highly eifective lubricating agents for yarns of cellulose acetate or other organic derivative of cellulose.
Other objects of this invention will be apparent from the following detailed description and claims.
The lubricating agents of this invention contain a mixture of eicosane and an amine salt of an acid phosphate of-a higher fatty alcohol. 'Advantageously, they also contain an amine salt of a higher fatty acid.
The lubricating compositions of this invention are preferably prepared by mixing the eicosane in molten condition with an ester-forming phosphorus acid derivative, such as phosphorus pentoxide, and adding to the mixture a higher fatty alcohol, in amount suflicient to form an acidic phosphate of said alcohol, together with a higher fatty acid, while maintaining the said mixture at an elevated temperature. Thereafter an amine is added to the mixture to form the salts of the acidic phosphate and of the higher fatty acid.
The amine used in the productionof the lubricating compositions preferably contains a hydroxyl group. Examples of suitable tertiary amines of this type are dibutylethanolamine, triethanolamine, diethylethanolamine and triisopropanolamine. Amines containing no hydroxyl substituents, e. g. N,N-diethylcyclohexylamine, may be used, if desired. Although optimum results have been obtained using tertiary amines, secondary amines such as diethylamine or diethanolamine may be employed instead.
The alcohol used to form the acidic phosphate ester advantageously contains at least12 carbon atoms, preferably about 14 to 20 carbon atoms. Mixtures of alcohols for example, blends of homologous or isomeric alcohols, may be employed if desired. Examples of suitable alcohols are octadecyl (stearyl), octadecenyl (oleyl), and hexadecyl (cetyl), or mixtures of the same. Examples of ester-forming phosphorus acid derivatives suitable for reaction with the alcohol are phosphorus pentoxide, which is preferred, and phosphorus tetroxide. Phosphorus pentachloride may also be used but is somewhat less desirable since it liberates corrosive hydrochloric acid during the esterificationreaction. The relative amounts of the ester-forming phosphorus acid derivative and the higher fatty alcohol may be such that the resulting ester contains about 1 to 2, preferably 1.3 to 1.6, higher fatty alcohol radicals per phosphorus atom.
The higher fatty acid used in the production of the higher fatty acid, about 10 to 40%, preferably about 20 to 25%. If desired, there may be employed a slight excess of amine over that necessary to form the salts of the acidic constituents. For best results the amount of amine is such that the pH of an aqueous dispersion of the composition, of 20 to 30% concentration, is about 7.5 to 8.5.
The lubricating compositions of this invention maybe applied to the filamentary material in any desired manner. For example, the composition may be applied as a molten mixture, as a solution in a volatile solvent, or, most desirably, as a dispersion in water. The amine salts of the phosphate esters and fatty acids act, in part, as emulsifying agents so that the composition disperses easily in water. Suitable concentrations of the composition in Water are, for example, 5 to 35%, preferably 20 to 30% by Weight. prepared by adding the heated molten lubricating .composition to cool water under strong agitation. sired, an additional emulsifying agent may be incorporated into the mixture to improve the stability of the dispersion. Examples of such emulsifying agents are those polyethylene oxide derivatives known as Igepal CA-630, Brij 30, Lipal 30W, BS- and Sp'an 85.
It has been found that aqueous emulsions or dispersions produced in accordance with this invention have superior,
cation reaction between the higher fatty alcohol and the I phosphorus pentoxide or other ester-forming phosphorus acid derivative. If the higher fatty acid is not present at this time, but is added after the esterification reaction has been substantiallycompleted, the resulting emulsion is much more viscous.
The lubricating compositions of this invention are particularly useful for use on filamentary materials of cellulose acetate of about 53 to 55% acetyl value, calculated as combined acetic acid. They may also be applied to filamentary materials of other organic derivatives of cellulose, e. g. other cellulose esters, such as cellulose triacetate, cellulose propionate, cellulose butyrate, cellulose acetate-propionate and cellulose acetate-butyrate, or cellulose ethers, such as ethyl cellulose or benzyl cellulose. They are also useful for the lubrication of other filamentary.
materials, such as polyamides, e. g'. nylon, polyesters such as polyethylene terephthalate and polymers and copolymers of acrylonitrile. The compositions may be applied to continuous filaments as they emerge, in the form of a yarn, from the spinning cabinet or metier in which they are formed. Similarly, they may be applied to tows, or relatively thick bundles, of continuous filaments before said bundles are severed into staple fibers of the desired length, or they may be applied to the staple fibers themselves at any desired stage in the processing of said staple fibers. Generally, the amount of the composition Advantageously, the aqueous dispersions are applied to the filamentary material is about 1 to 4%, based on the weight of said filamentary material.
The use of the lubricating compositions of this invention greatly reduces the drag occurring when filamentary materials are passed over guide surfaces. In fact, their application to cellulose acetate yarns has made it possible to knit such yarns in a highly successful manner on circular knitting machines under such drastic conditions as had previously precluded the use of cellulose acetate yarns carrying the conventional lubricating agents.
In addition, the lubricating compositions of this invention show practically no change in characteristics on aging, either in the presence or absence of small amounts of water, have practically no tendency to corrode black iron, have excellent antistatic properties, improve the flex abrasion characteristics of the filamentary material, and may be very easily removed from the filamentary material by scouring in water.
The following examples are given to illustrate the invention further. All proportions are by weight unless otherwise indicated.
Example I 33.6 parts of the crystalline product consisting predominantly of n-eicosane, having a melting point of 96.5 F. and having 10% and 90% boiling points of 383 F. and 410 F., respectively, measured at 10 mm. Hg absolute, sold under the name Eicosane by Atlantic Refining Company, are melted and 4.3 parts of finely divided phosphorus pentoxide are added thereto and mixed for 5 minutes to form a slurry. The temperature of the slurry is adjusted to 60 C. and then 24.4 parts of oleyl alcohol and 13.0 parts of oleic acid are added quickly. The ensuing reaction causes the temperature to rise. Then the mixture is heated further and maintained at a temperature of 80 C. for 30 minutes while it is stirred vigorously. Thereafter 19.8 parts of dibutylethanolamine and 4.9 parts of the emulsifying agent known as Igepal CA630 (a non-ionic nonyl phenoxy ether of a polyethylene glycol containing 8 to 12 ethoxy linkages) are blended into the mixture. On cooling the product is a soft wax. This soft wax is emulsified in water by heating the wax to 80 C., at which temperature it is molten, and then adding it, while stirring, to 4 times its weight of water having a temperature of 25 C. The emulsion is applied to dull cellulose acetate continuous filament yarn in amount sufiicient to deposit thereon 2.5%, based on the weight of the yarn. The yarn is then knitted on a Wildman Interlock circular knitting machine. Knitted fabrics of excellent quality are produced.
Example II Example I is repeated except that the Igepal CA-630 is omitted. The resulting mixture is applied in molten condition, at 35 to 40 C., to the yarn. The lubricating efiect is substantially the same as in Example 1.
Example III Example I is repeated except that 35 parts of eicosane are employed; 24.5 parts of stearyl alcohol and 13.2 parts of stearic acid are substituted for the oleyl alcohol and oleic acid, respectively; 18 parts of triethanolamine are substituted for the dibutylethanolamine; and the stearic acid is added after the stearyl alcohol has been reacted in the mixture for the 30 minute period. The product is a hard wax. This wax is emulsified by first mixing it thoroughly with twice its weight of water having a temperature of 80 C., to form a paste, cooling the paste and adding the desired amount of cold Water. The resulting composition has substantially the same lubricating properties as that of Example I.
Example I V Thirty parts of the triethanolamine ester of stearic acid and thirty parts of the triethanolamine salt of stearyl phosphate are mixed in forty parts of molten eicosane 4 until a homogeneous mixture results. On cooling, a hard wax results. This wax is .emulsified by first mixing it thoroughly with twice its weight of water having a temperature of 80 C., to form a paste, cooling the paste and adding the desired amount of cold water. The product has good lubricating properties.
It is to be understood that the foregoing detailed d scription is merely given by way of illustration and that many variations may .be made therein without departing from the spirit of our invention.
Having described our invention, what we desire to secure by Letters Patent is:
l. A lubricating composition for filamentary materials, comprising about 20 to 45 parts by weight ,of n-eicosane and about 25 to 45 parts by weight of an amine salt of an acid phosphate of a higher fatty alcohol.
2. Textile fibers carrying a coating of the lubricating composition of claim 1.
3. A lubricating composition for filamentary materials, comprising about 20 to 45% of n-eicosane, about 25 ,to 45 of an amine sale of an acid phosphate of a higher fatty alcohol, and about 10 to 40% of an amine salt of a higher fatty acid.
4. A lubricating composition for filamentary materials, comprising about 20 to 45 parts by weight of n-eicosane, about'25 to 45 parts by Weight of an amine salt of an acid phosphate of a higher fatty alcohol, and about 10 to 40 parts by weight of an amine salt of a higher fatty acid, dispersed to a concentration of about 20 to in an aqueous medium in the presence of a non-ionic emulsifying agent.
5. A lubricating composition as set forth in claim 3, said amine in each .case containing an alcoholic hydroxyl group.
6. A lubricating composition as set forth in claim 3, in which said amine is dibutylethanolamine.
7. A lubricating composition as set forth in claim 3, in which said amine is triethanolamine.
8. Cellulose acetate filamentary material carrying a coating of the lubricating composition of claim 3 in which the tertiary amine in each case contains an alcoholic hydroxyl group.
9. A lubricating composition for filamentary materials, comprising about 30 to of n-eicosane, about 3.0 to of a tertiary amine salt of an acid phosphate of oleyl alcohol, and about 20 to 30% of a tertiary amine salt of oleic acid, said tertiary amine in each case containing an alcoholic hydroxyl group.
10. A lubricating composition for filamentary materials, comprising about 35 to of n-eicosane, about 25 to 35% of a tertiary amine salt of an acid phosphate of stearyl alcohol, and about 25 to 35% of a tertiary amine salt of stearic acid, said tertiary amine in each case containing an alcoholic hydroxyl group.
11. Process for the production of lubricating compositions, which comprises forming a mixture of about 20 to 45 parts by weight of molten n-eicosane and an esterforming phosphorus acid derivative, adding to the mixture a higher fatty alcohol, in amount sufficient to react with said phosphorus acid derivative to form an acidic phosphate of said alcohol, while maintaining said mixture at an elevated esterification temperature, and thereafter adding an amine to the resulting mixture to form an amine salt of said acidic phosphate, said phosphorus acid derivative, higher fatty alcohol and amine being added in amount sufiicient to form about 25 to 45 parts by weight of the amine salt of said acidic phosphate.
12. Process for the production of lubricating compositions, which comprises forming a mixture of molten n-eicosane and an ester-forming phosphorus acid derivative, adding to the mixture a higher fatty alcohol, in amount sufiicient to react with said phosphorus acid derivative to form an acidic phosphate of said alcohol, together with a higher fatty acid, while maintaining said mixture atan elevated, esterification temperature, adding an amine to the resulting mixture to form amine salts of said acidic phosphate and said higher fatty acid, and thereafter emulsifying the mixture in Water.
13. Process as set forth in claim 12 wherein a nonionic emulsifying agent is present during said step of emulsifying.
14. Process as set forth in claim 12 in which said amine contains an alcoholic hydroxyl group and said phosphorus acid derivative is phosphorus pentoxide.
15. Process for the production of lubricating compositions, which comprises forming a mixture of about 20 to 45 parts by Weight of molten n-eicosane and an esterforming phosphorus acid derivative, adding to the mixture a higher fatty alcohol, in amount sufficient to react with said phosphorus acid derivative to form an acidic phosphate of said alcohol, together with a higher fatty acid, while maintaining said mixture at an elevated esteri- 'fication temperature, adding an amine to the resulting mixture to form amine salts of said acidic phosphate and said higher fatty acid, said phosphorus acid derivative, higher fatty alcohol, higher fatty acid and amine being added in amount sufiicient to form about to 45 parts by Weight of the amine salt of said acidic phosphate and about 10 to 40 parts by Weight of the amine salt of said higher fatty acid, and thereafter emulsifying the mixture in water to a concentration of about 20 to References Cited in the file of this patent UNITED STATES PATENTS 1,914,331 Nuesslein June 13, 1933 2,277,788 Shipp Mar. 31, 1942 2,676,924 Fortess Apr. 27, 1954 2,759,851 Pluck Aug. 21, 1956
Claims (1)
1. A LUBRICATING COMPOSITION FOR FILAMENTARY MATERIALS, COMPRISING ABOUT 20 TO 45 PARTS BY WEIGHT OF N-EICOSANE AND ABOUT 25 TO 45 PARTS BY WEIGHT OF AN AMINE SALT OF AN ACID PHOSPHATE OF A HIGHER FATTY ALCOHOL.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US492308A US2853451A (en) | 1955-03-04 | 1955-03-04 | Lubricating agents |
GB6608/56A GB789716A (en) | 1955-03-04 | 1956-03-02 | Lubricating agents for textiles |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US492308A US2853451A (en) | 1955-03-04 | 1955-03-04 | Lubricating agents |
Publications (1)
Publication Number | Publication Date |
---|---|
US2853451A true US2853451A (en) | 1958-09-23 |
Family
ID=23955770
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US492308A Expired - Lifetime US2853451A (en) | 1955-03-04 | 1955-03-04 | Lubricating agents |
Country Status (2)
Country | Link |
---|---|
US (1) | US2853451A (en) |
GB (1) | GB789716A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3113369A (en) * | 1960-05-02 | 1963-12-10 | Monsanto Chemicals | Yarn manufacture and products obtained thereby |
US3113887A (en) * | 1959-04-28 | 1963-12-10 | Mead Corp | Method for cast coating paper |
US3297570A (en) * | 1964-05-28 | 1967-01-10 | Eastman Kodak Co | Yarn treating compositions |
US3428481A (en) * | 1966-07-06 | 1969-02-18 | Du Pont | Antistatic lubricating composition for textile fibers |
US3475204A (en) * | 1967-09-18 | 1969-10-28 | Du Pont | Polyester tire cord lubricant |
US3634117A (en) * | 1968-02-17 | 1972-01-11 | Glanzstoff Ag | A textile material coated with an ammonium dialkyl phosphate antistatic agent |
US4618579A (en) * | 1984-09-28 | 1986-10-21 | Genencor, Inc. | Raw starch saccharification |
CN111040859A (en) * | 2019-12-25 | 2020-04-21 | 上海金兆节能科技有限公司 | High-temperature environment-friendly lubricating grease and preparation method thereof |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104695229B (en) * | 2015-03-06 | 2017-01-04 | 苏州爱立方服饰有限公司 | A kind of fabric inorganic agent and preparation method thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1914331A (en) * | 1929-12-18 | 1933-06-13 | Ig Farbenindustrie Ag | Treatment of textile materials with aqueous liquids |
US2277788A (en) * | 1940-08-03 | 1942-03-31 | Du Pont | Treatment of textiles and composition useful therefor |
US2676924A (en) * | 1952-06-04 | 1954-04-27 | Celanese Corp | Textile lubricant |
US2759851A (en) * | 1954-01-29 | 1956-08-21 | American Cyanamid Co | Water-repellent treatment for hydrophobic textile materials |
-
1955
- 1955-03-04 US US492308A patent/US2853451A/en not_active Expired - Lifetime
-
1956
- 1956-03-02 GB GB6608/56A patent/GB789716A/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1914331A (en) * | 1929-12-18 | 1933-06-13 | Ig Farbenindustrie Ag | Treatment of textile materials with aqueous liquids |
US2277788A (en) * | 1940-08-03 | 1942-03-31 | Du Pont | Treatment of textiles and composition useful therefor |
US2676924A (en) * | 1952-06-04 | 1954-04-27 | Celanese Corp | Textile lubricant |
US2759851A (en) * | 1954-01-29 | 1956-08-21 | American Cyanamid Co | Water-repellent treatment for hydrophobic textile materials |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3113887A (en) * | 1959-04-28 | 1963-12-10 | Mead Corp | Method for cast coating paper |
US3113369A (en) * | 1960-05-02 | 1963-12-10 | Monsanto Chemicals | Yarn manufacture and products obtained thereby |
US3297570A (en) * | 1964-05-28 | 1967-01-10 | Eastman Kodak Co | Yarn treating compositions |
US3428481A (en) * | 1966-07-06 | 1969-02-18 | Du Pont | Antistatic lubricating composition for textile fibers |
US3475204A (en) * | 1967-09-18 | 1969-10-28 | Du Pont | Polyester tire cord lubricant |
US3634117A (en) * | 1968-02-17 | 1972-01-11 | Glanzstoff Ag | A textile material coated with an ammonium dialkyl phosphate antistatic agent |
US4618579A (en) * | 1984-09-28 | 1986-10-21 | Genencor, Inc. | Raw starch saccharification |
CN111040859A (en) * | 2019-12-25 | 2020-04-21 | 上海金兆节能科技有限公司 | High-temperature environment-friendly lubricating grease and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
GB789716A (en) | 1958-01-29 |
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