EP1733079A1 - Fil de polyester continu a faible effet de meche - Google Patents
Fil de polyester continu a faible effet de mecheInfo
- Publication number
- EP1733079A1 EP1733079A1 EP05731588A EP05731588A EP1733079A1 EP 1733079 A1 EP1733079 A1 EP 1733079A1 EP 05731588 A EP05731588 A EP 05731588A EP 05731588 A EP05731588 A EP 05731588A EP 1733079 A1 EP1733079 A1 EP 1733079A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- filament
- yam
- less
- contact angle
- wicking
- 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.)
- Withdrawn
Links
- 229920000728 polyester Polymers 0.000 title claims description 14
- 230000003068 static effect Effects 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000004744 fabric Substances 0.000 claims abstract description 11
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 7
- 239000000975 dye Substances 0.000 claims description 6
- 229920013639 polyalphaolefin Polymers 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 4
- 229920002647 polyamide Polymers 0.000 claims description 4
- 229920006397 acrylic thermoplastic Polymers 0.000 claims description 3
- 239000002216 antistatic agent Substances 0.000 claims description 3
- 239000000314 lubricant Substances 0.000 claims description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 3
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000003139 biocide Substances 0.000 claims description 2
- 239000003086 colorant Substances 0.000 claims description 2
- 239000007822 coupling agent Substances 0.000 claims description 2
- 239000003063 flame retardant Substances 0.000 claims description 2
- 239000012760 heat stabilizer Substances 0.000 claims description 2
- 239000004611 light stabiliser Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 235000004879 dioscorea Nutrition 0.000 abstract description 26
- 238000000034 method Methods 0.000 abstract description 18
- 239000010902 straw Substances 0.000 abstract description 8
- 238000009941 weaving Methods 0.000 abstract description 2
- 239000000835 fiber Substances 0.000 description 19
- 229920000642 polymer Polymers 0.000 description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 150000002009 diols Chemical class 0.000 description 9
- -1 aromatic dicarboxylic acids Chemical class 0.000 description 8
- 230000008569 process Effects 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 238000009987 spinning Methods 0.000 description 5
- 229920002994 synthetic fiber Polymers 0.000 description 5
- 239000012209 synthetic fiber Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 230000002940 repellent Effects 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000009736 wetting Methods 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- QLRRUWXMMVXORS-UHFFFAOYSA-N Augustine Natural products C12=CC=3OCOC=3C=C2CN2C3CC(OC)C4OC4C31CC2 QLRRUWXMMVXORS-UHFFFAOYSA-N 0.000 description 2
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 239000003570 air Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 239000004597 plastic additive Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 229940035437 1,3-propanediol Drugs 0.000 description 1
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- WTKWFNIIIXNTDO-UHFFFAOYSA-N 3-isocyanato-5-methyl-2-(trifluoromethyl)furan Chemical compound CC1=CC(N=C=O)=C(C(F)(F)F)O1 WTKWFNIIIXNTDO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920006309 Invista Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- XDODWINGEHBYRT-UHFFFAOYSA-N [2-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCCCC1CO XDODWINGEHBYRT-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- PMMYEEVYMWASQN-IMJSIDKUSA-N cis-4-Hydroxy-L-proline Chemical compound O[C@@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-IMJSIDKUSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- XBZSBBLNHFMTEB-UHFFFAOYSA-N cyclohexane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCCC(C(O)=O)C1 XBZSBBLNHFMTEB-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- TVIDDXQYHWJXFK-UHFFFAOYSA-N n-Dodecanedioic acid Natural products OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 1
- YVBBRRALBYAZBM-UHFFFAOYSA-N perfluorooctane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YVBBRRALBYAZBM-UHFFFAOYSA-N 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Natural products OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/08—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with halogenated hydrocarbons
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/12—Layered products comprising a layer of synthetic resin next to a fibrous or filamentary layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/02—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
-
- 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
- D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine
-
- G—PHYSICS
- G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
- G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
- G09F17/00—Flags; Banners; Mountings therefor
-
- G—PHYSICS
- G09—EDUCATION; CRYPTOGRAPHY; DISPLAY; ADVERTISING; SEALS
- G09F—DISPLAYING; ADVERTISING; SIGNS; LABELS OR NAME-PLATES; SEALS
- G09F7/00—Signs, name or number plates, letters, numerals, or symbols; Panels or boards
Definitions
- filament yarns of the present invention have a wicking characteristic of about 6 mm or less, a contact angle of greater than or equal to about 65° but less than about 90°, and have a static voltage range of +/- 400 volts (a voltage between -400 to +400).
- Such filament yarns are made using an aqueous dispersion of a specific fluorocarbon surfactant, or a mixture of a few specific surfactants, that is used to impart water and oil repellency to synthetic fibers.
- Known fluorocarbon surfactants that impart water and oil repellency to synthetic fibers are not capable of achieving the wicking angle, contact angle and static voltage mentioned previously.
- fluorochemical emulsions and specifically fluorocarbon surfactant emulsions to impart oil and water resistance to synthetic fibers is well known. These treatments can be applied in the form of a spin finish to impart moisture resistance in fabric made from the fiber or continuous filament. Its use as a spin finish for carpet fibers, for example, is to impart water and oil repellency to the synthetic fibers.
- the following prior art illustrate these technologies.
- U. S. Patent 6,536,804 to Dunsmore et al. relates to carpet fibers in which a spin finish is applied to the synthetic staple fibers (not continuous filament yarn) for creating a surface on the carpet that is water and oil repellent.
- fluorochemicals were components of the spin finish.
- U. S. Patent Application Publication Number US 2003/0175514 to Hancock et al. discloses a low wicking type material that has use in fabrics, which are water repellent. Specific polymers disclosed are nylons, polyesters and polyolefins. This reference also discloses that a filament has a contact angle greater than or equal to 90° as measured by the method disclosed in the Journal of Colloid and Interface Science, 177, 579-588 (1996). This reference also discloses a filament having a coating thereon and wherein the contact angle of the coated filament is greater than or equal to 90°.
- the coating (described as the "second longitudinally-extending component of the filament”) can be virtually any halogenated polymer as disclosed in Paragraph 29.
- the polarity of the static voltage depends on the relative position of the yam and the rubbing surface on the triboelectric series.
- continuous filament yams having a static operating range of +/- 400 volts permits the continuous filament yams to be processed into a fabric in virtually any ambient air conditions, without the need of static eliminators in the fiber forming and fabric forming equipment, and because the continuous filament is drier, the processing equipment can be ran at faster output.
- the present invention teaches a filament ya that has low wicking, i.e., less than or equal to about 6 mm; has a contact angle of greater than or equal to about 65° but less than about 90° according to the straw method; and a static voltage of +/- 400 volts (between -400 to +400 volts).
- the preferred ya is continuous
- the yams of the present invention have a contact angle greater than or equal to about 65°, while yams of the prior art have contact angles less than about 65° or greater than about 90°.
- Those known low wicking continuous filament yams commercially available at the present time will not have wicking less than or equal to about 6 mm, a static voltage of +/- 400 volts, and a contact angle greater than or equal to about 65°.
- the contact angle test and evaluation are described by Augustine Scientific at Newbury, OH. Like all contact angle tests, the higher the degree, the more non wetting the continuous filament is.
- the sign of the static voltage will depend on the relative position of the type of ya and the rubbing surface on the triboelectric series. Generally polyester and nylon will be positively charged.
- Thermoplastic polymers useful for making synthetic fibers of this invention include fiber-forming polyesters, poly(alpha)olefins, polyamides and acrylics.
- Preferred thermoplastic polymers are polyesters are produced from the reaction of a diacid or diester component comprising at about 65 mole % terephthalic acid or d - C 4 dialkylterephthalate, preferable at least 70 mole %, and a diol component comprising at least about 65 mole % ethylene glycol, preferably at least 70 mole %, more preferably at least 75 mole %, even more preferably at least 95 mole %. It is also preferable that the diacid component is terephthalic acid and the diol component is ethylene glycol. The mole percentage for all the diacid component totals 100 mole %, and the mole percentage of all the diol component totals 100 mole %.
- suitable diol components of the described polyesters may be selected from 1 , 4-cyclohexanedimethanol, 1, 2-propanediol, 1 , 3-propanediol, 1 , 4- butanediol, 2, 2-dimethyl-l, 3-propanediol, 1, 6-hexanediol, 1, 2-cyclohexanediol, 1 , 4- cyclohexanediol, 1 , 2-cyclohexanedimethanol and diols containing one or more oxygen atoms in the chain, e.g., diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol or mixtures of these, and the like.
- these diols contain 2 to 18, preferable 2 to 8 carbon atoms.
- Cycloaliphatic diols can be employed in their cis or trans configuration or as mixtures of both forms.
- Preferred modifying diol components are 1 , 4-cyclohexanedimethanol or diethylene glycol, or a mixture of these.
- the suitable acid components (aliphatic, alicyclic, or aromatic dicarboxylic acids) of the linear polyester may be selected, for example, from isophthalic acid, 1, 4-cyclohexanedicarboxylic acid, 1, 3-cyclohexanedicarboxylic acid, succinic acid, glutaric acid, adipic acid, sebacic acid, 1 , 12-dodecanedioic acid, 2, 6- napthalenedicarboxylic acid, bibenzoic acid, or mixtures of these and the like.
- a functional acid derivative thereof such as the dimethyl, diethyl, or dipropyl ester of the dicarboxylic acid.
- the anhydrides or acid halides of these acids may also be employed where practical.
- thermoplastic polymers are poly(alpha)olefins, including the normally solid, homo-, co- and terpolymers of aliphatic mono- 1 -olefins (alpha olefins) as they are generally recognized in the art.
- the monomers employed in making such poly(alpha)olefins contain 2 to 10 carbon atoms per molecule, although higher molecular weight monomers sometimes are used as comonomers.
- Blends of the polymers and copolymers prepared mechanically or in situ may also be used.
- Examples of monomers that can be employed in the invention include ethylene, propylene, butene- 1 , pentene-1 , 4-methyl-pentene-l , hexene-1 , and octene-1 , alone, or in admixture, or in sequential polymerization systems.
- Examples of preferred thermoplastic poly(alpha)olefin polymers include polyethylene, polypropylene, propylene/ethylene copolymers, polybutylene and blends thereof. Polypropylene is particularly preferred for use in the invention.
- Typical polyamides suitable for this invention are nylon 6 and nylon 66.
- Processes for preparing the polymers useful in this invention are well known, and the invention is not limited to a polymer made with a particular catalyst or process.
- the process of melt spinning the multifilament yam is well known in the art.
- the molten polymer is fed under high pressure to the heated housing which accommodates the spinning.
- the molten polymer is forced through a number of spinning orifices provided in a spinneret.
- the filaments emerge from the spinneret as a bundle.
- the filament bundle may pass through a delay zone (heated or unheated) prior to a quench zone, in which the bundle is cooled with air of room temperature, which is blown onto the filaments transverse to the direction of movement of the bundle.
- the filament bundle is subsequently brought into contact with the finish metering unit in which a suitable lubricant is applied to the filaments of the bundle in the usual way.
- the multifilament bundle arrives at the first of a set of advancing rolls for imparting the correct speed to the yam bundle.
- the circumferential speed of the feed roll is determinative of the speed at which the filaments are spun and is therefore referred to as the spinning speed.
- the spun multifilament yam After the spun multifilament yam has left the rolls, it is wound into a package. The speed at which the yam is wound will be approximately equal to the spinning speed. After the yam has been taken up, it is drawn on a separate machine to the desired ratio. In principle, however, drawing also may be carried out on the spinning machine in a continuous spin-drawing process. In the event of the spin- drawing process known per se being applied a drawing device consisting of one or more driven rolls is to be provided between the first driven roll and the winding bobbin.
- plastic additives can also be added.
- plastic additives may be anti-static agents, biocides, coloring agents (dyes and pigments), coupling agents, flame retardants, heat stabilizers, light stabilizers, lubricants, plasticizers and mixtures of a plurality of these.
- Fluorocarbon based surfactants are amphiphilic materials containing an oleophobic and hydrophobic perfluorinated tail and a hydrophilic head. They are effective to reducing the surface tension of surfaces, since the oleophobic tail bonds to the polymer surface and the molecule orients perpendicular to the surface.
- a key variable in different fluorocarbon based surfactants is the number of carbon atoms in the perfluorinated tail of the compound. It is generally thought that longer chain (C 8 ) fluorochemical tails give lower surface reduction potentials than shorted chains. In the case of their use as spin finishes for fibers it is important that the fluorochemical gives a high surface coverage so that there are no bare areas along which the water can wick. Although not bound by theory, it is believed that the shorter chains take longer to organize and thus flow better on the polymeric fiber surface.
- the aqueous dispersion fluorocarbon chemicals used in the present invention are known by their trade names of Afilan 5248A and Afilan 5284B produced by Clariant. Additionally, trade names Lurol FC-L575 and FC-L790 produced from Goulston are likewise satisfactory. The aqueous dispersion fluorocarbon chemicals mentioned above are suitable for the present invention and provide these properties.
- aqueous dispersion fluorocarbon chemicals Mitsubishi Chemical Company (Repearl F89, a perfluoroalkyl polyacrylate copolymer emulsion), 3M (F359, a perfluoroctane based surfactant) have been tested but have been found to be lacking and do not provide a wicking of less than or equal to about 6 mm, a contact angle (as determined by the straw method) of about 65° or more, and a static voltage of less than or equal to +/- 400 volts. Since these are proprietary spin finishes, the detailed differences are not known. It was surprising that there was a difference between the various fluorocarbon based finishes.
- the aqueous dispersion fluorocarbon chemicals are applied to the fibers as a spin finish, for example.
- the aqueous dispersions are prepared to give about 15 % by weight solids with the remainder being water.
- spin finishes are suitable for the present invention.
- Wicking is determined by the distance that a dye solution wicks up the vertically suspended yam.
- a 0.5 wt-% aqueous dye solution of Palanil Cerise NSL 200 (BASF Corporation) is prepared.
- a paper clip (0.5 g) is tie to one end of the yam and suspended into a 50 ml beaker.
- the dye solution is added to the beaker so that it just covers the knot. After 45 minutes, the yam is lifted out of the beaker and allowed to dry. The amount of wicking above the knot as indicated by the dye line is measured.
- the contact angle is determined by the straw method, as explained by Augustine
- the contact angle is the quantitative measure of wet-ability for a solid surface being wetted with a liquid, which ranges from 0 (perfect wetting) tol 80° (complete non-wetting).
- the contact angle using the straw method is measured by using several fibers each having a length of about 7.5 cm, which are laid together. A thin flexible copper wire is looped around the fibers and both ends of the wire are fed through a small piece of tubing (the
- Teflon tubing having a small inner diameter of about 1mm and a length of roughly 25 mm is employed.
- the wire is pulled so that the fibers are forced to double over on themselves and enter the tube.
- Enough fibers are used so that the tube becomes fairly tightly packed with fibers.
- the fibers are trimmed off evenly at the bottom end of the tube and the wire is removed from the fiber loop that is created at the top end of the tube.
- the tube containing the fibers is attached to the balance (Kriiss
- the static voltage is measured by running the ya a half turn around a 6.35 mm diameter ceramic (aluminum oxide) pin at yam speed of 300 meters per min. with a pretension of about 65 g.
- the static generated is measured 48 mm from the threadline with a Monroe Electronics static voltmeter.
- the temperature of the test conditions is 70° F with a relative humidity of 40%.
- polyester industrial ya s with different finish types, were compared. All yams were prepared by applying the spin finish (15% emulsion in water) to the spun yam and used a spin-draw process. The target final finish on yam was 0.4 to 0.6 wt- %. The yam dtex was 1100 with 140 filaments. The yam had a tenacity of 70 cN/tex, a breaking elongation of 25 % and a hot air (177° C, 30 min.) shrinkage of 3.5 %.
- the control is a commercial Type 787 (INVISTA, Salisbury NC, U.S.A.) which used a finish consisting of a blend of a thermally stable polyol ester, ethoxylated non-ionic emulsifiers and a cationic antistatic agent.
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- General Physics & Mathematics (AREA)
- Theoretical Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
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Abstract
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US55511104P | 2004-03-22 | 2004-03-22 | |
PCT/US2005/008989 WO2005093140A1 (fr) | 2004-03-22 | 2005-03-18 | Fil de polyester continu a faible effet de meche |
Publications (2)
Publication Number | Publication Date |
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EP1733079A1 true EP1733079A1 (fr) | 2006-12-20 |
EP1733079A4 EP1733079A4 (fr) | 2008-10-01 |
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Application Number | Title | Priority Date | Filing Date |
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EP05731588A Withdrawn EP1733079A4 (fr) | 2004-03-22 | 2005-03-18 | Fil de polyester continu a faible effet de meche |
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EP (1) | EP1733079A4 (fr) |
JP (1) | JP2007530804A (fr) |
KR (1) | KR100878578B1 (fr) |
CN (1) | CN1934295A (fr) |
BR (1) | BRPI0508949A (fr) |
MX (1) | MXPA06009900A (fr) |
WO (1) | WO2005093140A1 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7494709B2 (en) | 2005-03-18 | 2009-02-24 | Performance Fibers Operations, Inc. | Low wick continuous filament polyester yarn |
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PT2510148E (pt) | 2009-12-09 | 2013-11-06 | Teijin Aramid Bv | Uso de partículas do tipo núcleo-invólucro para aplicação anti-absorção de um fio ou pano |
CN102978733A (zh) * | 2012-12-15 | 2013-03-20 | 浙江海利得新材料股份有限公司 | 一种抗芯吸型低收缩涤纶工业丝及其制备方法 |
KR101649421B1 (ko) * | 2014-12-25 | 2016-08-22 | 주식회사 효성 | 발수 성능이 향상된 고강도 폴리에스테르 원사와 그 제조방법 |
CN105926082A (zh) * | 2016-06-27 | 2016-09-07 | 吴江耀迪纺织品有限公司 | 一种石墨烯发热阻燃纺织品风管 |
CN106317448B (zh) * | 2016-08-22 | 2019-04-05 | 盐城市天马日用品有限公司 | 一种可变色抗菌海绵的制备方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993002235A1 (fr) * | 1991-07-23 | 1993-02-04 | Eastman Kodak Company | Fibres aptes a transporter spontanement des liquides |
WO2000032854A1 (fr) * | 1998-12-03 | 2000-06-08 | The Dow Chemical Company | Fibres et tissus thermoplastiques |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US6630087B1 (en) | 2001-11-16 | 2003-10-07 | Solutia Inc. | Process of making low surface energy fibers |
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2005
- 2005-03-18 WO PCT/US2005/008989 patent/WO2005093140A1/fr active Application Filing
- 2005-03-18 BR BRPI0508949-2A patent/BRPI0508949A/pt not_active Application Discontinuation
- 2005-03-18 EP EP05731588A patent/EP1733079A4/fr not_active Withdrawn
- 2005-03-18 MX MXPA06009900A patent/MXPA06009900A/es unknown
- 2005-03-18 KR KR1020067022001A patent/KR100878578B1/ko not_active IP Right Cessation
- 2005-03-18 CN CNA2005800091086A patent/CN1934295A/zh active Pending
- 2005-03-18 JP JP2007505020A patent/JP2007530804A/ja active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993002235A1 (fr) * | 1991-07-23 | 1993-02-04 | Eastman Kodak Company | Fibres aptes a transporter spontanement des liquides |
WO2000032854A1 (fr) * | 1998-12-03 | 2000-06-08 | The Dow Chemical Company | Fibres et tissus thermoplastiques |
Non-Patent Citations (1)
Title |
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See also references of WO2005093140A1 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7494709B2 (en) | 2005-03-18 | 2009-02-24 | Performance Fibers Operations, Inc. | Low wick continuous filament polyester yarn |
Also Published As
Publication number | Publication date |
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MXPA06009900A (es) | 2007-04-13 |
WO2005093140A1 (fr) | 2005-10-06 |
EP1733079A4 (fr) | 2008-10-01 |
CN1934295A (zh) | 2007-03-21 |
KR100878578B1 (ko) | 2009-01-15 |
KR20070026470A (ko) | 2007-03-08 |
BRPI0508949A (pt) | 2007-10-16 |
JP2007530804A (ja) | 2007-11-01 |
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