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
  • D06M13/165—Ethers
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
  • 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
• • 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

Definitions

• the invention relates to a fiber lubricant, a fatty acid ester of an alkoxylated phenol derivative, which has effective thermal and oxidative stability, non-volatility, product stability and, in a preferred embodiment, emulsification properties and which when applied to a fiber, as a fiber lubricant formulation, exhibits effective viscosity and lubricity.
• a fiber lubricant formulation consists of a base material, or lubricant, such as mineral oil, alkyl esters of fatty acids or vegetable oils; emulsifiers that allow the lubricant to be applied from a water solution; antistatic agents; antioxidants; bacteriocides; friction modifiers; and buffering agents.
• a fiber lubricant is critical to the conversion of nylon or polyester fiber into useful yarn for textile manufacturing.
• the fiber lubricant has several functions. One function is to control friction.
• the fiber lubricant may protect the newly spun fiber from fusion or breakage by controlling the yarn-to-metal friction at frictional contact points between the yarn and machine guides, rollers, draw plates, heater plate and texturing false twist spindles or friction discs.
• the lubricant also functions to provide yarn cohesion giving strength to the yarn by holding the yarn bundled together and by allowing the yarn to build up an acceptable package at the end of processing. Static electricity that is formed as the yarn rapidly moves through the processing equipment would also be controlled.
• the lubricant must also protect machine surfaces from wear.
• U.S. 4,165,405 discloses fiber lubricants based upon fatty esters of heteric polyoxyalkylated alcohols wherein mononuclear, monofunctional initiators are alkoxylated and then esterified.
• U.S 4,127,490 relates to lubricating fibers with a major amount of lubricant and a minor amount of a stabilizer, said stabilizer being the reaction product of one mole of dicyclopentadiene and at least one mole of p-cresol, further reacted with at least one-half mole of isobutylene.
• U.S. 4,252,528 relates to a spin finish for synthetic fibers of a thermally stable lubricant and a surfactant derived from an ethylene oxide-propylene oxide block copolymer adduct of an alkylated phenol.
• U.S. 4,252,528 relates to a spin finish for synthetic fibers of a thermally stable lubricant and a surfactant derived from an ethylene oxide-propylene oxide block copolymer adduct of an alkylated phenol.
• 3,578,594 relates to a fiber treating composition ccnsisting essentially of about 90 percent to about 25 percent by weight of at least one ester of an ethoxylated aliphatic alcohol and about 10 percent to about 75 percent by weight of at least one ester of an ethoxylated arylphenol.
• the examples relate to a-methyl benzyl phenol or bis ⁇ -methyl benzyl phenol as the aryl phenol.
• a problem of the prior art fiber lubricants mentioned above is that they are not disclosed as being capable of being used alone or in a water emulsion as a fiber lubricant formulation. None of the above references discloses the use as a fiber lubricant of the products of applicants' invention, nor do they suggest the use of applicants' product alone or as a water emulsion.
• a purpose of the invention was to provide a fiber lubricant which may be used by itself in pure form as a fiber lubricant formulation.
• Another purpose of the invention was to provide a self-emulsifiable fiber lubricant for use as a fiber lubricant formulation.
• a fiber lubricant has been discovered having effective thermal and oxidative stability, non-volatility, product stability, and, in a preferred embodiment, emulsification properties, and which when applied to a fiber, as a fiber lubricant formulation, exhibits effective viscosity and lubricity.
• the fiber lubricant is useful as a fiber lubricant formulation in pure application to polyester or nylon fiber during a drawing and texturing operation.
• the fiber lubricant formulation is used in a process of lubricating synthetic fibers which comprises applying the fiber lubricant to the fiber in an amount between 0.05 percent by weight and 5 percent by weight, based on the weight of the lubricated fiber.
• the fiber lubricant comprises a compound selected from the group consisting of wherein A is an oxyalkylene radical having 2 carbon atoms to 4 carbon atoms or mixtures thereof, R is hydrogen or acyl containing from 8 carbon atoms to 22 carbon atoms, R' is alkyl containing from 1 carbon atom to 10 carbon atoms, R'' is alkyl containing from 1 carbon atom to 22 carbon atoms, R''' is alkyl containing from 4 carbon atoms to 8 carbon atoms and R''''' is R" or R''', X is an alkylidene radical containing from 1 carbon atom to 3 carbon atoms and n is an integer such that the molecular weight of the compound is between 500 and 2500 and,with the proviso that either R'' or R''' is ortho to the oxygen in formula III.
• the oxyalkylene radical is oxyethylene or a mixture of oxyethylene and up to 50 percent by weight of an oxyalkylene radical having 3 carbon atoms to 4 carbon atoms and provides effective hydrophilicity to the compound to enable it to self emulsify in water.
• the lubricants of the present invention are prepared from three essential ingredients, i.e., certain phenol derivatives, alkylene oxides and fatty acids.
• phenol derivatives are compounds selected from the group consisting of the following formulas: wherein X, R', R'', R''' and R''' are as described above.
• X alkylidene radicals such as methylene, ethylene and propylidene.
• R' and R'' are methyl and isobutyl.
• R''' and R''' are butyl and octyl.
• phenol derivative of formula V is a compound wherein X is as the phenol derivative of formula VI is a compound wherein x is as the phenol derivative of formula VII is a compound wherein R'' is C 4 H 9 -, R''' is C 8 H 17 - and R'''' is C 8 H 17 - or C 4 H 9 - or a compound wherein R'' is C 4 H 9 -, R''' is C 4 H 9 - and R'''' is CH 3 - and as the phenol derivative of formula VIII is a compound wherein X is R' is CH 3 - and R " is C 4 H 9 -.
• alkylene oxides from which the oxyalkylene radical derives, are alkylene oxides containing 2 carbon atoms to 4 carbon atoms such as ethylene oxide, propylene oxide and butylene oxide.
• alkylene oxides containing 2 carbon atoms to 4 carbon atoms such as ethylene oxide, propylene oxide and butylene oxide.
• Useful in a preferred embodiment is ethylene oxide or a mixture of ethylene oxide and other alkylene oxides which when used in a mixture with ethylene oxide impart a hydrophilicity effective to self emulsify the compound.
• other 3 or 4-carbon cyclic ethers such as tetrahydrofuran, oxetane, and methyl oxetane may be used.
• Preferaby used are mixtures of ethylene oxide and propylene oxide.
• the oxyalkylene is present in the fiber lubricant in an amount, as represented by n, such that the molecular weight of the compound is between 500 and 2500.
• n such that the molecular weight of the compound is between 500 and 2500.
• fatty acids are those containing between 8 carbon atoms and 22 carbon atoms, preferably between 16 and 20 carbon atoms and more preferably 18 carbon atoms, such as isostearic acid.
• the phenol derivative is ethoxylated by adding the phenol derivative and a basic catalyst to an autoclave evacuated to a vacuum and pressurized with nitrogen and equipped with temperature, pressure and vacuum controls, and thereafter heated.
• the alkylene oxide is added at a constant rate until all the oxide is added.
• the reaction then proceeds at a temperature between 90°C and 130°C until a constant pressure is observed.
• Esterification is then accomplished by adding approximately equal molar amounts of fatty acid and alkoxylated phenol derivative.
• Acid catalysts such as methane sulfonic acid and hypophosphorus acid are added and the esterification reaction is allowed to proceed at a constant temperature, such as 165°C under a nitrogen blanket.
• the lubricants of this invention are applied to the fiber in an amount between 0.05 percent by weight and 5 percent by weight, based on the weight of the lubricated fiber.
• the lubricity of the products of this invention on synthetic yarns may be determined using any reasonable method.
• One useful test method measures the lubricity, in units of the coefficient of friction, of nylon filaments having fiber lubricants applied to them at a concentration of about 1 percent lubricant by weight of filament by the procedure of the following two paragraphs.
• a stable aqueous emulsion of the lubricant is prepared.
• This emulsion is applied to the yarn, such as nylon or polyester, using an apparatus in which the yarn is passed at a controlled speed through a continually replenished drop of finished solution or dispersion of specified concentration.
• a suitable apparatus is the ATLAS yarn finish applicator sold by the Precision Machine and Development Company of Wilmington, Delaware.
• the lubricant dispersion is metered to the continually replenished drop of solution using a syringe pump.
• Tne yarn is fed over an adjustable canter roller which functions to space the yarn over a drying drum used to remove water.
• the yarn is finally passed over a winding tube and subsequently conditioned for 16 to 24 hours at 65 percent relative humidity and 70°F before being tested.
• the coefficient of friction (f) may be determined on any suitable machine, such as a Rothschild F Meter utilizing 0.313 inch diameter ceramic (Al Si Mg) and satin chrome friction pins that has friction surface at a yarn contact angle of 180°.
• the yarn speed is varied, such as at 50, 100, 150, 200, and 250 meters per minute.
• the yarn tension may be varied such as at 4 or 6 grams on the input side as determined by tensiometers by the Rothschild F meter.
• the (f) values are determined directly by reading the chart produced by the Rothschild F meter.
• Viscosity may be determined by any standard procedure, such as using a Brookfield viscometer or Ubelohde tube following ASTM D444 71/79 or D2161-79.
• the viscosity of the fiber lubricants of this invention have a controlled viscosity range, from 500 to 1500 Saybolt universal seconds. A viscosity below this range is detrimental to processing the fibers and a viscosity above this range causes excessive add-on to the fibers.
• Thermal and oxidative stability as well as non-volatility of the fiber lubricant may be tested by a number of suitable procedures such as the hot plate test, the circulating air oven test, dynamic thermogravimetric analysis and isothermal thermogravimetric analysis.
• the hot plate test proceeds by placing metal cups, 3 for each example, on a heater and maintaining the temperature at 240°C for 24 hours. At intervals of time, the weight loss for each of the 3 samples is determined and averaged and the quality of residue determined.
• the hot plate test is representative of thermal stability as measured by the results at 240°C for 24 hours and of oxidative stability by the quality of the residue.
• the circulating air oven test proceeds as in the hot plate test except the hot plate and samples are placed in a circulating air oven.
• thermogravimetric analyses proceed as follows: the dynamic thermogravimetric analysis measures the temperature in degrees centigrade at which a specific percentage by weight, such as 1 percent by weight and 10 percent by weight, of the sample is lost in a test atmosphere, such as air or nitrogen, while heating the sample at a constant heating rate, such as 20 degrees per minute; and the isothermal thermogravimetric analysis measures the percent by weight loss of the sample at a constant temperature, such as 210°C, for a specific time interval, such as 40 minutes, while the. sample is continuously weighed.
• the product stability of the fiber lubricant may be tested by any suitable method.
• the ability of the product of the invention to be storage stable is excellent.
• the emulsification properties of the fiber lubricant may be tested by preparing a mixture containing 10 parts of fiber lubricant, 20 parts of mineral oil and 70 parts of water. The mixture is shaken vigorously and allowed to stand for 24 hours. If separation of the emulsion does not occur, the emulsion is considered stable.
• the products of a preferred embodiment of the invention are self emulsifiable with water and do not require additives to make an emulsion.
• Additional additives may, however, be added to the fiber lubricants in preparing fiber lubricant formulations. These additives are described in U.S. 4,134,841.
• Example 1 of this invention the isostearate ester of ethoxylated butylated styrenated cresol, a specific product containing compounds of formula IV above, was obtained having a hydroxyl number of 4.4, an acid number of 1.56 and a viscosity of 781 Saybolt universal seconds at 100°F.
• A is a polyoxypropylene block adduct of a polyoxyethylene adduct of ethylene glycol of approximate average molecular weight of the hydrophobe of 1000 and an oxyethylene content of about 50 percent by weight.
• B is a polyoxyethylene block adduct of a polyoxypropylene adduct of propylene glycol of approximate average molecular weight of the hydrophobe of 950 and an cxyethylene content of about 50 percent by weight.
• C is a heteric ethylene oxide propylene oxide adduct of a C12-C15 fatty alcohol, having an overall approximate average molecular weight of 1280 and containing about 50 percent ethylene oxide.
• D is a polyoxyethylene block adduct of a polyoxypropylene adduct of bisphenol A of approximate average overall molecular weight of 8350 and an oxyethylene content of about 80 percent by weight.
• Lubricity, heat stability and emulsion properties were obtained as follows: An aqueous emulsion of the lubricant of Example 1 was prepared. This emulsion was applied to yarn using an Atlas yarn finish applicator. The coefficient of friction (f) was determined on a Rothschild F meter utilizing 0.313 inch diameter ceramic (Al Si Mag) and satin chrome friction pins as the friction surface at a yarn contact angle of 180°. The ASTM procedure Standard Test Method for Coefficient Friction, Yarn to Metal Designation 03108-76 was generally followed. The lubricity results, using 40/12 denier nylon 6 yarn, are shown in Table I for the products of Example 1 and comparison Example A.
• Stable emulsions made with the product of Example 1, and water and with the product of Example 1, water and other materials'are shown in Table V.
• Examples 3-10 and 14-19 were prepared using the procedure to prepare Example 1A.
• Examples 2, 11 - 13 and 20 were prepared using the procedure for preparing the product of Example 1.
• EO is ethylene oxide
• PO is propylene oxide
• product Y 1 is a commercial product of formula V wherein X is (WINGSTAY® S - Goodyear Company)
• product Y 2 is a commercial product of formula VII wherein R" is C 4 H 9 -, R''' is C 8 H 17 - and R'''' is either C 4 H 9 - or C 8 H 17 -(WINGSTAY® T - Goodyear Company)
• product Y 3 is a commercial product of formula VI wherein X is and R" is C 4 H 9 - (WINGSTAY® C - Goodyear Company).

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

Applications Claiming Priority (2)

Publications (2)

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ID=23426011

Family Applications (1)

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Citations (2)

• 1983
  • 1983-03-17 EP EP83102632A patent/EP0090273A3/de not_active Withdrawn
  • 1983-03-25 CA CA000424456A patent/CA1219252A/en not_active Expired

Patent Citations (2)

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