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
  • 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
  • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
  • D06M15/647—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
• • 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
  • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
  • D06M15/227—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated
• • 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
  • D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
• • 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

• This invention pertains to a liquid composition that may be applied to threads and plied yarns using kiss roll application methods.
• the composition does not require heat to liquify it during the application and provides superior performance over traditional "hot melt” compositions.
• wax/silicone coating is placed on a thread to improve certain characteristics of the thread such as the breaking strength, coefficient of friction, amount of wear and to add antistatic properties.
• the wax/silicone coating is applied to the thread by two methods known in the art; kiss roll (hot melt) methods and exhaust finish methods.
• the kiss roll application methods comprise using a mixture comprising a wax, a linear polydimethylsiloxane and a stabilizer or surfactant.
• the mixture which is typically a solid at room temperature, is heated to liquify. The mixture is then picked up on a roller across which the thread is drawn before being wound onto a spool.
• One of the disadvantages of these "hot melt” mixtures is that they must be heated prior to application.
• Another disadvantage to using a hot melt mixture is that the thread winders must be run at significantly slow speeds to prevent slinging off of the mixture. When the mixture splatters it solidifies and creates a clean up problem which results in costly clean up time.
• the exhaust finish application methods use an emulsion comprising a wax, a linear polydimethylsiloxane, water and a cationic surfactant.
• the wax may be added to the emulsion as, a solid or it may be pre-emulsified in water.
• These emulsions are liquid at room temperature and usually contain large amounts of water in the continuous phase.
• the exhaust finish emulsions are applied by placing the emulsion in a bath and then dipping a "spool" of thread into the bath and allowing it to sit in the bath for a period of time until the active ingredient is fully exhausted onto the thread and a clear liquid remains. Typically the bath of the emulsion is heated during the application period.
• the thread is then dried and wound onto the final spools.
• the exhaust emulsions typically provide superior thread sewing performance results than the kiss roll mixtures.
• the exhaust finish emulsions are higher priced, they are cationic and therefore lead to waste water problems, they are difficult for the thread manufacturers to handle and they typically do not result in an even application on the thread.
• U.S. Patent No. 4,434,008 to Dumm et al. teaches an exhaust emulsion composition comprising, on a water free basis, (a) about 5 to 80 weight percent of a silicone oil having a viscosity of from about 500 to 50,000 mm2/sec at 25°C.; (b) about 10 to 80 weight percent of a wax with a melting point of not less than about 40°C.; (c) about 1 to 10 weight percent of fatty acids with 6 to 22 carbon atoms; (d) about 0.4 to 12 weight percent of cationic imidazolinium salts; and (e) from about 0 to 10 weight percent of ethoxylated fatty amines.
• composition is produced by emulsifying (in water) the silicone oil with a portion of the fatty acid and imidazolinium salt and emulsifying (in water) the wax with the remainder of the fatty acid and imidazolinium salt and them combining the two emulsions together.
• the compositions typically comprise 30 percent or more water in the continuous phase.
• This invention pertains to a liquid composition
• a liquid composition comprising (A) a silicone oil having a viscosity of 5 to 5,000 centistokes at 25°C.; (B) a wax emulsion; and (C) a silicone surfactant.
• This liquid composition can be applied to threads and plied yarns (herein referred to as threads) using kiss roll methods.
• Component (A) of this composition is a silicone oil with a viscosity of 5 to 5,000 centistokes at 25°C., preferably 20 to 100 centistokes at 25°C.
• the silicone oil preferably is a linear dimethylpolysiloxane oil.
• a portion of the methyl groups can be replaced by alkyl groups with a longer chain length and/or by phenyl groups.
• the terminal chain ends of the silicone oil are typically formed by trimethyl silyl groups. However, hydroxyl groups may be present on the terminal chain ends.
• the silicone oil is typically present in the composition at level of 50 to 95 percent by weight, preferably 60 to 80 percent by weight.
• the silicone oils can be exemplified by, but not limited to, polydimethylsiloxanes, DOW CORNING 200 FLUIDS, hydroxyl endblocked polydimethylsiloxanes and mixtures thereof.
• Component (B) of this invention is a wax emulsion comprising a wax which typically has a melting point of higher than 40°C. and water.
• Useful waxes are petroleum waxes such as a paraffin waxes, microcrystalline waxes and semicrystalline waxes; synthetic waxes such as polyethylene waxes, Fischer-Tropsch Waxes (polyethylene), and chemically modified hydrocarbon waxes (ester waxes); natural waxes such as beeswax and carnauba; and mixtures thereof.
• the waxes are supplied as an emulsion in water typically comprising 10 to 80 percent by weight of the wax, preferably 50 to 80 percent by weight.
• Preferred wax emulsions are those that contain paraffin at levels of 50 to 70 percent by weight.
• the emulsions of the waxes may be produced using methods known in the art or they are commercially available.
• the wax emulsion is typically present at 5 to 40 percent by weight based on the total composition.
• the wax emulsions may be exemplified by Rayolan CPN produced by Boehme Filatex, Inc. (50% paraffin, cationic), Uscosoft HTW produced by Ivax Inc. (28% High Density Polyethylene Emulsion), Uscosoft LPD produced by Ivax Inc. (40% Low Density Polyethylene Emulsion), Michem Emulsion 47960 produced by Michelman Industries (60% paraffin, nonionic), Emulsion 150-50 produced by Chemical Corporation of America (50% paraffin, m.p. 150°F., nonionic), and Emulsion 135-50 produced by Chemical Corporation of America (50% paraffin, m.p. 135°F., nonionic).
• Component (C) is an silicone surfactant.
• Silicone surfactants are well known in the art. For example they may be polydiroganosiloxane-polyoxyalkylene copolymers such as those described in U.S. Patent No. 4,265,878 to Keil; organopolysiloxane-polyoxyalkylene block copolymers such as those described in U.S. Patent No. 4,532,132 to Keil; and siloxane copolymers such as those described in U.S. Patent No. 4,087,478 to Keil.
• the silicone surfactant is usually used at levels of 0.5 to 5, percent by weight based on the total composition.
• the liquid composition of this invention is prepared by thoroughly dispersing the organic compatible silicone surfactant (C) with the silicone oil (A) using agitation or other similar means. The wax emulsion is then added into the silicone oil/surfactant mixture. The final composition is then dispersed or emulsified using a homogonizer, sonolator or other dispersion means.
• the liquid compositions of this invention are useful for thread lubricants which are applied using kiss roll application methods.
• the liquid composition is typically applied on the thread at concentration of 2 to 15 percent by weight of the thread, depending on the type of thread being treated.
• concentration 2 to 15 percent by weight of the thread, depending on the type of thread being treated.
• One skilled in the art will be able to determine the amount necessary to create the best properties in the thread. Since the composition is liquid, it is not necessary to heat them for the application however, mild heat, preferably less than 50°C., can be used if desired.
• Table 1 Four liquid compositions in Table 1 were prepared by mixing a silicone surfactant, DOW CORNING Q2-3201 SURFACTANT, with a polydimethylsiloxane (350 cs at 25°C.) until homogeneous. The wax emulsion was added and the mixture was agitated vigorously for an additional 15 minutes. The compositions were applied to a spun polyester thread at a 5% add on level using an ATLAB finish applicator (simulated kiss roll application method). The treated thread was evaluated for the Drag Value (the value that relates to final tension of the thread after it has been pulled over the guilds of an industrial sewing machine). The value reported is an average of the three measurements. The drag value was also measured on untreated thread and on a thread that was treated with a commercially available exhaust finish emulsion which was applied using exhaust finish technology. Results are given in Table 1.
• a silicone surfactant DOW CORNING Q2-3201 SURFACTANT
• a liquid composition was prepared by mixing 81 parts of a polydimethylsiloxane having a viscosity of 50 centistokes at 25°C. with 2 parts of a silicone surfactant, DOW CORNING Q2-3201 INTERMEDIATE, until the silicone surfactant is well dispersed.
• a silicone surfactant DOW CORNING Q2-3201 INTERMEDIATE
• Michem Emulsion 47960 produced by Michelman Industries was added slowly and stirred for 30 minutes. The resulting mixture was passed through a sonolator at 800 PSI, 0.001 orifice.
• the liquid composition, Sample XV was applied at a 5.6% finish level to pink, black and white spun polyester sewing thread using a kiss roll applicator. Thread count was 41/2.
• a comparative test was also done by applying a nonionic silicone/wax emulsion, 50% solids, to the same type of thread at a 5% solids level using a kiss roll applicator. Results are given in Table 3. Corrosion and mildew are problems identified with use of the comparative fluid.
• Example XV The same liquid composition that was prepared in Example 3 (Sample XV) was applied to a spun polyester (spun poly) arid a polyester wrapped polyester (poly/poly) thread at a 8% finish level using a kiss roll applicator.
• a commercially used hot melt silicone/wax product 100% solids, was applied at an 8% finish level using the kiss roll applicator.
• Example XV The same liquid composition that was prepared inExample 3 (Sample XV) was applied to a polyester wrapped polyester (poly/poly) thread at a 6% finish level using a kiss roll applicator.

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• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Engineering & Computer Science (AREA)
• Textile Engineering (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
• Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
• Chemical Treatment Of Fibers During Manufacturing Processes (AREA)
• Compositions Of Macromolecular Compounds (AREA)

Applications Claiming Priority (2)

Publications (2)

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Family Applications (1)

Country Status (3)

Cited By (4)

Citations (4)

• 1991
  • 1991-09-02 JP JP22153091A patent/JPH04281072A/ja not_active Withdrawn
  • 1991-09-03 EP EP19910308068 patent/EP0474467B1/de not_active Expired - Lifetime
  • 1991-09-03 DE DE1991610216 patent/DE69110216T2/de not_active Expired - Fee Related

Patent Citations (4)

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