US2253146A - Method of sizing synthetic linear polymer yarns - Google Patents
Method of sizing synthetic linear polymer yarns Download PDFInfo
- Publication number
- US2253146A US2253146A US237789A US23778938A US2253146A US 2253146 A US2253146 A US 2253146A US 237789 A US237789 A US 237789A US 23778938 A US23778938 A US 23778938A US 2253146 A US2253146 A US 2253146A
- Authority
- US
- United States
- Prior art keywords
- acid
- yarns
- yarn
- interpolymer
- filaments
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000004513 sizing Methods 0.000 title description 33
- 238000000034 method Methods 0.000 title description 15
- 229920000642 polymer Polymers 0.000 title description 14
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 40
- 239000000203 mixture Substances 0.000 description 37
- 239000004952 Polyamide Substances 0.000 description 33
- 229920002647 polyamide Polymers 0.000 description 33
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 31
- 239000004744 fabric Substances 0.000 description 27
- 239000004753 textile Substances 0.000 description 25
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 22
- 230000015572 biosynthetic process Effects 0.000 description 17
- 238000009940 knitting Methods 0.000 description 17
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 13
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 12
- 229920002125 Sokalan® Polymers 0.000 description 12
- 239000004584 polyacrylic acid Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 11
- 150000001875 compounds Chemical class 0.000 description 11
- 230000008569 process Effects 0.000 description 11
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 10
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 238000009877 rendering Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 239000000314 lubricant Substances 0.000 description 7
- 229920000570 polyether Polymers 0.000 description 7
- 229920002302 Nylon 6,6 Polymers 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 238000009958 sewing Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 238000005096 rolling process Methods 0.000 description 5
- 238000004826 seaming Methods 0.000 description 5
- 235000011187 glycerol Nutrition 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- -1 sulfuric acid ester Chemical class 0.000 description 4
- URAYPUMNDPQOKB-UHFFFAOYSA-N triacetin Chemical compound CC(=O)OCC(OC(C)=O)COC(C)=O URAYPUMNDPQOKB-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 108010013296 Sericins Proteins 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000004375 Dextrin Substances 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010622 cold drawing Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 235000019425 dextrin Nutrition 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000001087 glyceryl triacetate Substances 0.000 description 2
- 235000013773 glyceryl triacetate Nutrition 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 229940049964 oleate Drugs 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229960002622 triacetin Drugs 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- ICLYJLBTOGPLMC-KVVVOXFISA-N (z)-octadec-9-enoate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCC\C=C/CCCCCCCC(O)=O ICLYJLBTOGPLMC-KVVVOXFISA-N 0.000 description 1
- GVNWZKBFMFUVNX-UHFFFAOYSA-N Adipamide Chemical compound NC(=O)CCCCC(N)=O GVNWZKBFMFUVNX-UHFFFAOYSA-N 0.000 description 1
- 241001589086 Bellapiscis medius Species 0.000 description 1
- 241001665400 Coracias abyssinicus Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- HDIFHQMREAYYJW-XGXNLDPDSA-N Glyceryl Ricinoleate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OCC(O)CO HDIFHQMREAYYJW-XGXNLDPDSA-N 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 235000013877 carbamide Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- QKDVBBQDDNJDSH-UHFFFAOYSA-N ethanol;formamide Chemical compound CCO.NC=O QKDVBBQDDNJDSH-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 229940117013 triethanolamine oleate Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000009736 wetting 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
- 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
- D06M15/244—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
-
- 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
- D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
Definitions
- This invention relates to a new and improved sizing composition for such textile filaments and yarns as are quite insensitive to water and to which the usual sizing compositions adhere with difliculty.
- These filaments are insoluble'in substantially all common solvents and are little affected by contact with water; the ratio of their wet strength
- the manufacture of fine stockings is, at best, a delicate operation and the cost of the finished product is a reflection vof the convenience of opdown after leaving the needles and sinkers resultto their dry strength being much higher than for other textile filaments.
- Another very interesting and useful property of these filaments is their ability to become set in the condition or shape in which they are first exposed to. steam, hot water, hot alcohols and other non-solvent swelling agents. After a setting treatment the filaments when deformed tend to return, after the deforming forces are removed, tothe shape inwhich they were set.
- the synthetic linear polyamides are of two types, those obtainable from mono-aminomonocarboxylic acids and those obtainable from the reaction of suitable diamines and dibasic carboxylic acids.
- the diamine-dibasic acid derivatives are more fully described in the U. S. Patent No. 2,130,948.
- this invention shall be discussed in'terms of these polyamides, particularly of polyhexamethylene adipamide which is obtainable from the reaction of hexamethylene diamine and adipic acid, although the invention is not so limited.
- the object of this invention is to provide a sizing composition for polyamide yarns which will promote good snag resistance, which will definitely reduce edge rolling of the flat knit fabric and which will make for good final'stitch formation.
- the object of the invention is accomplished by the use of a'sizing composition comprising polyalphamethacrylic acid.
- polymethacrylic acid preparation of the polyalphamethacrylic acid, hereinafter referred to as polymethacrylic acid, is not within the scope of this invention, a suitable polymer may be conveniently prepared by direct polymerization of the purified monomeric material in water.
- the monomeric material has the formula This solution of the polymer may be used directly without isolation of the polymethacrylic acid or it may also be used in solution in organic solvents.
- the natureof the invention will become more acrylic acid (having a viscosity of 4.5 poises in methyl alcohol solution) in ethyl alcohol on a Wildman full-fashioned knitting machine.
- the yarn was moistened just before it reached the needles and sinkers of the knitting machine by passing it over a wick wet with water. This moistenlng rendered the sizing composition plas- The v tic and facilitated good loop formation. humidity and temperature of the knitting room was so adjusted that the knit fabric dried sufficiently to destroy the plasticity of the sizing composition before :the fabric was removed from the knitting machine thus holding the desired loop formation in the fabric until it could be set;- Similarhi sized polyhexamethylene adipamide yarns of the proper denier and twist were used in the toe, welt, heel and sole. This fabric had little edge roll, good snag resistance, well formed stitches, and open loops. Following knitting, the
- stocking was looped and seamed in the customary manner, placed on a boarding form and' treated with saturated steam to set the yarn in the ,desired conformation. The stocking was then removed from the form and subjected to scouring, dyeing, rinsing, finishing and reboarding operations. The completed stocking had an attractive appearance, excellent stitch formation and good fabric elasticity.
- Example 11 A skein of denier, 20-turn polyhexamethylene adipamide yarn was treated as in Example I in an aqueous bath containing 8% polymethacrylic acid, 10% triacetin and 0.2% of Gardinol WA (the sodium salt of sulfuric acid ester I of lauryl alcohol).
- the yarn was used in knitting stocking fabric on a Wildman full-fashioned knitting machine. The yarn was moistened just before knitting and'the knitted fabric was dried immediately after it left the needles and sinkers by a current of warm air. The yarn knit well, producing a fabric of excellent stitch formation which showed practically no edge rolling and which had no pulled threads.
- Example III An aqueous solution was prepared containing 6% of polymethacrylic acid, 4% of glycerol, and 0.5% of Textile Softener No. 3 (a' commercial water-emulsifiable mineral oil). This solution was applied to a polyhexamethylene adipamide' yarn on a spool to spool sizing machine in which the yarn was taken fromv a twister pirn A sewing thread was prepared by plying together three l-denier, '75-filament, 12-turn S" twist oriented polyhexamethyleneadipamide yarns with 8 turns Z twist.
- the sewing thread was then treated as inExample I in an aqueous bath containing 10 g./liter of'polymethacrylic acid and 10 g./liter of glycerin and 0.6% of a mixture of 50% oleyl diethyl ethylene di'amine ethyl sulfate. and 50% dextrin, and dried at room temperature.
- the resulting sewing thread performed very well at high speeds, did not undergo appreciable abrasion on commercial sewing machines and gave seams of good strength. Sewing threads so prepared are valuable for use in the looping and seaming of these synthetic polyamide stockings.
- polymethacrylic acid adheres to the yarn, which adhesion is a strict requirement for a size. That polymethacrylic acid adheres to the yarn is surprising, considering the fact that the acid can be applied from a water solution, and that the filaments are notably insensitive to water and other common solvents, not to speak of the fact that the filaments are slick and smooth, which in itself complicates the sizing problem.
- the size compositions of this invention are capable of being easily and rapidly dried at a reasonably low temperature so that there is little danger of prematurely setting 'the polyamide yarn, which setting would tend to seriously interfere with good final stitch formation.
- the size is also capable of being easily softened by moisture .so'that a temporary condition of plasticity can be developed at the moment of knitting, after which it can be readily dried, reducing the plasticity' and holding the stitches in the desired conformation until they can be set.
- the rapid rate at which yarns sized with these tions may be dried effects an important in the sizing operation. This is especially true in continuous sizing operations permitting size applications at a very rapid rate.
- the size is capable of sofincomposiishing the yarn and of so holding the filaments together as a unitary structure as to resist snagging during the operation of knitting, looping, seaming, topping, etc., to the end that a stocking is produced which is free from pulled threads and, therefore, a high stockings is assured.
- the flat knit stocking sized with the composition has a greatly reduced tendency to roll on itself with the result that the 1 looping and seaming operation can be performed very simply and quickly and without the pro- ,fductionof snags which would certainly resultif a considerable amount of manipulation was reeconomy percentage of satisfactory the balloon of the downtwister.
- the softness and smoothness of the treated yam may be modified by the addition of material, such as glycerol, glycols, esters of glycerol, such as triacetin and glyceroltriglycollate, sulfonated oils, dextrin, urea, ethanol formamide, etc.
- material such as glycerol, glycols, esters of glycerol, such as triacetin and glyceroltriglycollate, sulfonated oils, dextrin, urea, ethanol formamide, etc.
- wetting agents such as Gardinol" WA, may be added to the composition if desired.
- Theinvention also contemplates the addition of lubricants to the composition where the presence of a lubricant on the flnalyarn is found desirable. Itis true that the sizing of the yarn permits the filaments to operate as a unitary structure, prevents the formation of pulled threads bysetting up a snag resistance, insures Similarly, the invention has poration of a textile lubricant in the compositions. Materials which are suitable for this purpose are mineral, vegetable, and sulfonated oils, soaps, such as triethanolamine oleate, and a variety of other materials such as diglycol oleate, glycerol monoricinoleate, etc.
- the lubricants added to the sizing composition can also be added before or after and independent of the size composition.
- Various coning oils may .be applied to the yarns sized according to the invention.
- examples of such compositions include olive, tea seed and and at the same time act as a lubricant and/or wetting agent.
- some of the modifiers mentioned may act as buffers to maintain at any desired value the pH of the size bath or of the size on the yarn when moistened prior to knitting. That the size composition is not strongly acid is generally desirable to prevent undue corrosion of the needles and sinkers on the knitting machine.
- Other corrosion inhibitors may be added. Examples of other materials which may be added to the wetting trough of the knitting machine for various purposes include commercial triethanoi amine and its fatty acid esters, diglycol oleate, morpholene, pyridine, etc.
- the invention contemplates the use of a sizing composition for these polyamide yarns which comprises polymethacrylic acid and certain interpolymers of methacrylic acid, or in less preferred sizing compositions, polyacrylic acid.
- a sizing composition for these polyamide yarns which comprises polymethacrylic acid and certain interpolymers of methacrylic acid, or in less preferred sizing compositions, polyacrylic acid.
- the invention contempiates a polyamide yarn well sized and well capable of being used in textile operations as may be desired and where a size performs a useful function. It will. be found that the size adheres well to the yarn and resists mechanical removal which might result from the forces involved in a twisting operation or by rubbing against thread guides, etc.
- the sizing composition of this invention is also valuable in the treatment of textile filaments composed of other synthetic linear polymers includingpolyesters, polyethers, polyacetals, mixed polyesterpolyamides, etc., which, for example, may be prepared by a process of condensation polymetrizationas described in U. S. Patent No. 2,071,250.
- These sizing compositions are also suitable for sizing of filaments and yarns composed of the polymers prepared'by high pressure polymerization of ethylene which are described in the copending application of Fawcett et al., Serial No. 123,722,'filed February 2, 1937; also for sizing yarns of ingrain sllkin view of the definite advantage of ease of removal over sericin.
- a textile yarn comprising filaments of a crystalline syntheticlinear polymer taken from the class consisting of polyesters, polyethers and polyamides containing a coating of a sizing composition comprising a compound taken from the group consisting of polymethacrylic acid, an interpolymer of methacrylic acid with acrylic acid, polyacrylic acid, an interpolymer of methacrylic acid with. less than 10% of styrene, an interpolymer of methacrylic acid with less than 10% of vinyl acetate and an interpolymer of methacrylic acid with less than 10% of methyl methacrylate.
- a textile yarn comprising filaments of a crystalline synthetic linear polymer taken from the class consisting of polyesters, polyethers and polyamidescontaining 2% to 6% by weight of a coating of a compound taken from the group of styrene, an interpolymerof methacrylic acid consisting of polymethacrylic acid, an interpolymer of methacrylic acid with acrylic acid, polyacrylic acid, an interpolymer of methacrylic acid with less than 10% of styrene, an interpolyamides containing 2% to 6% of a coating of polymethacrylic acid.
- a textile yarn comprising filaments of a crystalline synthetic linear polyamide containing a coating of a sizing composition comprising a compound taken from the group consisting of polymethacrylic acid, an interpolymer of methacrylic acid with acrylic acid, polyacrylic acid, an interpolymer of methacrylic acid with less than 10% of styrene, an interpolymer of methacrylic acid with less than 10% of vinyl acetate and an interpolymer of methacrylic acid with less than 10% of methyl methacrylate.
- a textile yarn comprising filaments of a crystalline synthetic linear polyamide containing 2% to 6% by weight of a coating of a compound taken from the group consisting of polymethacrylic acid, an interpolymer of methacrylic acid with acrylic acid, polyacrylic acid, an interpolymer of methacrylic acid with less than 10% with less than 10% of vinyl acetate and an interpolymer of methacrylic acid with less than 10% of methyl methacrylate.
- a textile yarn comprising filaments of a crystalline synthetic linear polyamide containing a coating of asizing composition comprising polymethacrylic acid.
- a textile yarn comprising filaments of a crystalline synthetic linear polyamide containing 2% to 6% of a coating of polymethacrylic acid.
- a textile yarn comprising polyhexamethyl-.
- a sizing composition comprising a compound taken from the group consisting of polymethacrylic acid, an interpolymer of methacrylic acid with acrylic acid, polyacrylic acid, an interpolymer of methacrylic acid with less than of styrene, an interpolymer of methacrylic acid with les than 10% of vinyl acetate and an interpolymer of methacrylic acid with less than 10% of methyl methacrylate.
- the process of rendering textile yarns comprising filaments of a crystalline synthetic linear polyamide resistant to snagging and capable of being knit into fabrics'which will retain a uniform loop formation which comprises applying to said yarns a compound taken from the group consisting of polymethacrylic acid, an interpolymer of methacrylic acid with acrylic acid, polyacrylic acid, an interpolymer of methacrylic acid with less than 10% of styrene, an interpolymer of methacrylic acid with less than 10% of vinyl acetate and an interpolymer of methacrylic acid with less than 10% of methyl methacrylate.
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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)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL51855D NL51855C (enrdf_load_stackoverflow) | 1938-10-29 | ||
US237789A US2253146A (en) | 1938-10-29 | 1938-10-29 | Method of sizing synthetic linear polymer yarns |
DEP79914D DE757623C (de) | 1938-10-29 | 1939-10-20 | Praeparieren von Fasern, Faeden oder Garnen aus synthetischen linearen Polymeren, insbesondere Polyamiden, fuer die textile Weiterverarbeitung |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US237789A US2253146A (en) | 1938-10-29 | 1938-10-29 | Method of sizing synthetic linear polymer yarns |
Publications (1)
Publication Number | Publication Date |
---|---|
US2253146A true US2253146A (en) | 1941-08-19 |
Family
ID=22895187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US237789A Expired - Lifetime US2253146A (en) | 1938-10-29 | 1938-10-29 | Method of sizing synthetic linear polymer yarns |
Country Status (3)
Country | Link |
---|---|
US (1) | US2253146A (enrdf_load_stackoverflow) |
DE (1) | DE757623C (enrdf_load_stackoverflow) |
NL (1) | NL51855C (enrdf_load_stackoverflow) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2470039A (en) * | 1945-05-04 | 1949-05-10 | Edward E Lovig | Apparatus and process for making filaments |
US2606845A (en) * | 1949-04-09 | 1952-08-12 | Du Pont | Process for adhering polyvinyl chloride coatings to nylon fabric |
US2674547A (en) * | 1951-03-10 | 1954-04-06 | Us Rubber Co | Coated article and process of making same |
US2686137A (en) * | 1951-11-26 | 1954-08-10 | Monsanto Chemicals | Sized yarn and process of sizing |
US2690407A (en) * | 1951-05-25 | 1954-09-28 | Rca Corp | Method of preventing accumulation of static charges |
US2692182A (en) * | 1951-04-14 | 1954-10-19 | Rohm & Haas | Durable, stiff finish for nylon and method for producing same |
US2727835A (en) * | 1952-07-31 | 1955-12-20 | Monsanto Chemicals | Process of sizing synthetic yarn with hydrolyzed polyalkyl acrylates |
US2936249A (en) * | 1954-07-01 | 1960-05-10 | American Enka Corp | Process for conferring antistatic properties to synthetic textile fibers |
DE1109132B (de) * | 1958-11-21 | 1961-06-22 | Roehm & Haas Gmbh | Schlichtemittel fuer synthetische Fasern |
US3090664A (en) * | 1958-03-31 | 1963-05-21 | Du Pont | Graft polymerizing an unsaturated organic acid or salt thereof onto a nitrogen containing polymer substrate |
US3297471A (en) * | 1965-04-08 | 1967-01-10 | Du Pont | Acrylic or methacrylic acid grafting copolymerized on nylon and forming salt of said graft |
US3511677A (en) * | 1963-02-28 | 1970-05-12 | Du Pont | Process for preparation of a sized zero-twist synthetic fiber yarn and product thereof |
US3855776A (en) * | 1971-06-22 | 1974-12-24 | Asahi Chemical Ind | Synthetic thermoplastic multifilament yarns |
US3974321A (en) * | 1974-06-20 | 1976-08-10 | Diamond Shamrock Corporation | Yarn sizing process and product |
-
0
- NL NL51855D patent/NL51855C/xx active
-
1938
- 1938-10-29 US US237789A patent/US2253146A/en not_active Expired - Lifetime
-
1939
- 1939-10-20 DE DEP79914D patent/DE757623C/de not_active Expired
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2470039A (en) * | 1945-05-04 | 1949-05-10 | Edward E Lovig | Apparatus and process for making filaments |
US2606845A (en) * | 1949-04-09 | 1952-08-12 | Du Pont | Process for adhering polyvinyl chloride coatings to nylon fabric |
US2674547A (en) * | 1951-03-10 | 1954-04-06 | Us Rubber Co | Coated article and process of making same |
US2692182A (en) * | 1951-04-14 | 1954-10-19 | Rohm & Haas | Durable, stiff finish for nylon and method for producing same |
US2690407A (en) * | 1951-05-25 | 1954-09-28 | Rca Corp | Method of preventing accumulation of static charges |
US2686137A (en) * | 1951-11-26 | 1954-08-10 | Monsanto Chemicals | Sized yarn and process of sizing |
US2727835A (en) * | 1952-07-31 | 1955-12-20 | Monsanto Chemicals | Process of sizing synthetic yarn with hydrolyzed polyalkyl acrylates |
US2983628A (en) * | 1954-07-01 | 1961-05-09 | American Enka Corp | Process for conferring antistatic properties to dielectric products |
US2936249A (en) * | 1954-07-01 | 1960-05-10 | American Enka Corp | Process for conferring antistatic properties to synthetic textile fibers |
US3000758A (en) * | 1954-07-01 | 1961-09-19 | American Enka Corp | Process for conferring antistatic properties and the resulting products |
US3090664A (en) * | 1958-03-31 | 1963-05-21 | Du Pont | Graft polymerizing an unsaturated organic acid or salt thereof onto a nitrogen containing polymer substrate |
DE1109132B (de) * | 1958-11-21 | 1961-06-22 | Roehm & Haas Gmbh | Schlichtemittel fuer synthetische Fasern |
US3511677A (en) * | 1963-02-28 | 1970-05-12 | Du Pont | Process for preparation of a sized zero-twist synthetic fiber yarn and product thereof |
US3297471A (en) * | 1965-04-08 | 1967-01-10 | Du Pont | Acrylic or methacrylic acid grafting copolymerized on nylon and forming salt of said graft |
US3855776A (en) * | 1971-06-22 | 1974-12-24 | Asahi Chemical Ind | Synthetic thermoplastic multifilament yarns |
US3974321A (en) * | 1974-06-20 | 1976-08-10 | Diamond Shamrock Corporation | Yarn sizing process and product |
Also Published As
Publication number | Publication date |
---|---|
NL51855C (enrdf_load_stackoverflow) | |
DE757623C (de) | 1963-08-20 |
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