TWI237670B - Spinning and winding of polyester multifilament yarns using spinning additives and polyester multifilament yarns obtainable by the spinning process - Google Patents
Spinning and winding of polyester multifilament yarns using spinning additives and polyester multifilament yarns obtainable by the spinning process Download PDFInfo
- Publication number
- TWI237670B TWI237670B TW092104464A TW92104464A TWI237670B TW I237670 B TWI237670 B TW I237670B TW 092104464 A TW092104464 A TW 092104464A TW 92104464 A TW92104464 A TW 92104464A TW I237670 B TWI237670 B TW I237670B
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- Taiwan
- Prior art keywords
- patent application
- yarn
- item
- scope
- temperature
- Prior art date
Links
- 238000004804 winding Methods 0.000 title claims abstract description 56
- 229920000728 polyester Polymers 0.000 title claims abstract description 33
- 238000009987 spinning Methods 0.000 title claims description 34
- 239000000654 additive Substances 0.000 title abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 51
- 229920000642 polymer Polymers 0.000 claims abstract description 31
- 229920002215 polytrimethylene terephthalate Polymers 0.000 claims abstract description 19
- 229920001707 polybutylene terephthalate Polymers 0.000 claims abstract description 15
- 238000003860 storage Methods 0.000 claims abstract description 14
- -1 polybutylene terephthalate Polymers 0.000 claims abstract description 13
- 230000007774 longterm Effects 0.000 claims abstract description 4
- 238000010438 heat treatment Methods 0.000 claims description 34
- 238000001816 cooling Methods 0.000 claims description 15
- 239000004753 textile Substances 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 238000009835 boiling Methods 0.000 claims description 5
- 238000009941 weaving Methods 0.000 claims description 4
- 239000012744 reinforcing agent Substances 0.000 claims description 3
- 230000000172 allergic effect Effects 0.000 claims 1
- 208000010668 atopic eczema Diseases 0.000 claims 1
- 235000013351 cheese Nutrition 0.000 claims 1
- 239000013589 supplement Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 abstract description 6
- 239000003623 enhancer Substances 0.000 abstract description 4
- 230000008569 process Effects 0.000 abstract description 4
- 229920001577 copolymer Polymers 0.000 description 31
- 239000007789 gas Substances 0.000 description 26
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 18
- 239000000178 monomer Substances 0.000 description 13
- 239000000835 fiber Substances 0.000 description 12
- 239000000155 melt Substances 0.000 description 12
- 229920002959 polymer blend Polymers 0.000 description 11
- 238000005491 wire drawing Methods 0.000 description 10
- 238000012545 processing Methods 0.000 description 8
- 238000004512 die casting Methods 0.000 description 7
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 6
- 230000009477 glass transition Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 230000008901 benefit Effects 0.000 description 5
- 238000007664 blowing Methods 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 238000000465 moulding Methods 0.000 description 5
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 239000012774 insulation material Substances 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- 150000003440 styrenes Chemical class 0.000 description 4
- 229920002994 synthetic fiber Polymers 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 229910045601 alloy Inorganic materials 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 229910052702 rhenium Inorganic materials 0.000 description 3
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000012209 synthetic fiber Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-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
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000009529 body temperature measurement Methods 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Chemical group CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- VKYUUJCJFNLIMX-UHFFFAOYSA-N 6,6,6-triphenylhexanoic acid Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(CCCCC(=O)O)C1=CC=CC=C1 VKYUUJCJFNLIMX-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- QDHHCQZDFGDHMP-UHFFFAOYSA-N Chloramine Chemical compound ClN QDHHCQZDFGDHMP-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical class CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- 241001303620 Diphyes Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical class CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000945534 Hamana Species 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- 241000269799 Perca fluviatilis Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- CDMXXXZRZWQJQE-UHFFFAOYSA-N acetic acid;2-methylprop-2-enoic acid Chemical class CC(O)=O.CC(=C)C(O)=O CDMXXXZRZWQJQE-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical group CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000007707 calorimetry Methods 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000000112 cooling gas Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000003446 memory effect Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical group O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 229910052704 radon Inorganic materials 0.000 description 1
- SYUHGPGVQRZVTB-UHFFFAOYSA-N radon atom Chemical compound [Rn] SYUHGPGVQRZVTB-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 229940098465 tincture Drugs 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000010913 used oil Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 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
Classifications
-
- 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
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
- D01F6/92—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyesters
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D10/00—Physical treatment of artificial filaments or the like during manufacture, i.e. during a continuous production process before the filaments have been collected
- D01D10/02—Heat treatment
-
- 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
- D01F6/62—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyesters
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Mechanical Engineering (AREA)
- Artificial Filaments (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
Abstract
Description
12376701237670
(發明所屬之技術領域) 本發明是有關內含不少於85重量%聚對苯二甲酸丁 二醇酯(PBT)及/或聚對苯二甲酸丙二醇酯(PTMT)( 最好是PTMT)的聚酯絲,其旋轉抽絲與纏繞方法以及聚 酯多絲的製造方法,此外,本發明還述及聚酯多絲的拉伸 變形加工(DRAW TEXTURING)。 聚酯多絲特別是聚對苯二甲酸乙二醇酯(PET)多絲 的二階段連續生產方法已舉世皆知,其中第一階段包括旋 轉抽絲與纏繞及第二階段將多絲拉伸、熱處理或拉伸變形 爲大宗多絲紗,纏繞後的多紗包(PACKAGE)於上述兩 階段間的長時間儲存與高溫下的搬運都不會對第二階段的 加工或產品的品質發生影響。 F. FOURNE在其1995年所著的 ''合成纖維〃一書中 (慕尼黑HANSER出版)對此曾就基本面加以評述。 不過,PTMT或PBT的多紗與PET多紗不同,不但在 旋轉抽絲與纏繞之後,而且在纏繞後幾個小時、幾天,在 儲存與搬運,特別是高溫下的儲存與搬運後,展現相當大 的收縮傾向,因此,紗會短少,紗包會緊縮,於最嚴重之 時,紗包還會變硬,無法自纏繞機取下,在長時間儲存或 特別在高溫下搬運過程中,紗包還會失去其乳酪般外形, 成一馬鞍狀,即周邊硬而中間凹陷,結果,絲的材質會變 壞,紗包退繞時還會發生其他問題,這些不會發生在PET 纖維加工時的問題,一般來說,如要預防其發生,祗有限 制紗包重量於二公斤以下始可。 0續次頁(發明說明頁不敷使用時,請註記並使用顧) 7 1237670 發明說明續頁 立即自線軸上取出,且在儲存四週或在65°C高溫, 特別是在聚合物玻璃轉換點與65°C溫度間運送之後 ’仍能保持其原來外形。 -在高紡絲速度下仍能比不用添加劑時獲得較高破裂 伸長率,是故,用較高的拉伸比率仍能在進一步加 工中收此法的經濟效益。 -其得到的0 - 10%POY沸騰收縮率是以保證在儲存 中有高的穩定性,甚至縱在高達65°C溫度下沸騰收 縮也不致減少在10%以上(絕對値),所以纏繞後 紗包不會變形。 -經拉伸變形加工而得的紗是有高破裂伸長與高的破 裂強度。 現在要就本發明作更詳細的說明,有時要參考附件的 圖式: 圖1圖示一個裝置,用來抽取或纏繞一或多條多絲紗 〇 圖2圖示一個乳酪狀的紗包。 圖3圖示一變形的紗包,其特徵似一馬鞍,周邊堅硬 而中間似腰。 本發明提供一生產及纏繞聚酯多絲紗的方法。聚酯絲 中至少須含85重量%的聚對苯二甲酸丁二醇酯(PBT)及 /或聚對苯二甲酸丙二醇酯(PTMT)。熟悉本技術領域的 人都知道PBT與PTMT。其中PBT是由對酸與同莫爾量 的I,4 丁二醇聚凝結而成。而PTMT是由對酸與同莫爾釁 12 1237670(Technical Field to which the Invention belongs) The present invention relates to containing not less than 85% by weight of polybutylene terephthalate (PBT) and / or polytrimethylene terephthalate (PTMT) (preferably PTMT) The polyester yarn has a spinning drawing and winding method and a method for manufacturing a polyester multifilament. In addition, the present invention also refers to a drawing process of the polyester multifilament (DRAW TEXTURING). The two-stage continuous production method of polyester multifilament, especially polyethylene terephthalate (PET) multifilament, is well known in the world. The first stage includes spinning and winding and the second stage stretches the multifilament. 2. Heat treatment or tensile deformation into bulk multi-filament yarns. The long-term storage of the wrapped multi-package (PACKAGE) between the above two stages and the handling at high temperature will not affect the processing or product quality in the second stage. . F. FOURNE commented on the fundamentals in his 1995 book "Synthetic Fibers" (published by HANSER, Munich). However, PTMT or PBT multi-yarn is different from PET multi-yarn. It is not only after spinning and winding, but also for several hours and days after winding, during storage and handling, especially after storage and handling at high temperature. Quite large shrinkage tendency, therefore, the yarn will be short and the yarn package will shrink. At the worst, the yarn package will harden and cannot be removed from the winding machine. During long-term storage or especially during high temperature handling, The gauze bag also loses its cheese-like shape, forming a saddle shape, that is, the periphery is hard and hollow in the middle. As a result, the silk material will deteriorate, and other problems will occur when the gauze is unwound. These will not occur during PET fiber processing. In general, if you want to prevent it from happening, you have to limit the weight of the gauze to less than two kilograms. 0 Continued pages (Note when the invention description page is not enough, please note and use Gu) 7 1237670 Invention description The continuation page is immediately taken out from the spool, and stored around or at 65 ° C, especially at the polymer glass transition point After transportation to 65 ° C, it can still maintain its original shape. -At high spinning speeds, a higher elongation at break than when no additives are used is obtained, so the higher economic ratio can still be used to obtain the economic benefits of this method in further processing. -The obtained 0-10% POY boiling shrinkage is to ensure high stability during storage, and it will not be reduced above 10% (absolutely) even at temperatures up to 65 ° C, so after winding The yarn package will not deform. -Yarn obtained by tensile deformation processing has a high breaking elongation and a high breaking strength. Now to make a more detailed description of the present invention, sometimes reference is made to the drawings of the accessories: Figure 1 illustrates a device for extracting or winding one or more multi-filament yarns. Figure 2 illustrates a cheese-like yarn package . Figure 3 illustrates a deformed gauze bag, which is characterized by a saddle, with a rigid periphery and a waist-like center. The invention provides a method for producing and winding a polyester multifilament yarn. The polyester yarn must contain at least 85% by weight of polybutylene terephthalate (PBT) and / or polytrimethylene terephthalate (PTMT). Those skilled in the art know PBT and PTMT. Among them, PBT is formed by polycondensation of acid and I, 4 butanediol with the same molar amount. And the PTMT was challenged by the acid and the same Moore 12 1237670
的1,3丙二醇聚凝結而成。也可以混合使用此二聚酯。依 據本發明,比較傾向使用PTMT。 聚酯可以是單質聚合物或共聚物。有用的共聚物包括特 別是含有15莫爾%的PBT或PTMT,共單體的重複單元 ,例如乙二醇、二甘醇、三甘醇、1,4_環己烷二甲醇、聚 乙二醇、異酸及/或己二酸。對本發明而言,最好是使用 單質聚合物聚酯。 本發明的聚酯也可以進一步的包含慣常劑量的添加物 作爲混合配料,如催化劑、穩定劑、抗靜電劑、抗氧化劑 、火焰延遲劑、染料、染料增強劑、光穩定劑、有機燐、 光亮劑及去光澤劑。最好是,聚酯含有〇到5重量%的添 加劑。 聚酯也可以進一步的包含小量的,最好是不超過0.5 重量%的支鏈成分。依據本發明,最好的支鏈成分包括多 功能酸,如三苯六竣酸、或焦苯六羧酸,或三到六價酒精 ,羥甲基丙烷、季戊四醇、二季戊四醇、甘油、或相對應 的氫氧酸。 依據本發明,PBT及/或PTMT是與0·05重量%至 2.5重量%的添加聚合物相混合作爲延伸增強劑。爲了本 發明的這個目的特別有用的添加聚合物包含下列特定的聚 合物或共聚物: 1.聚合物是由單體物經聚合而成,其一般方程式如下 1237670 _ 發明說明續頁1,3 propylene glycol is made by coagulation. It is also possible to mix and use these two polyesters. According to the present invention, the use of PTMT is preferred. The polyester may be a simple polymer or a copolymer. Useful copolymers include, in particular, 15 mol% of PBT or PTMT, repeating units of comonomers such as ethylene glycol, diethylene glycol, triethylene glycol, 1,4-cyclohexanedimethanol, polyethylene glycol Alcohol, isoacid and / or adipic acid. For the present invention, it is preferred to use a simple polymer polyester. The polyester of the present invention may further include a conventional amount of additives as a mixing ingredient, such as a catalyst, a stabilizer, an antistatic agent, an antioxidant, a flame retarder, a dye, a dye enhancer, a light stabilizer, an organic tincture, a brightener. Agent and delustering agent. Preferably, the polyester contains 0 to 5% by weight of additives. The polyester may further contain a small amount of branched components, preferably not more than 0.5% by weight. According to the present invention, the preferred branched chain components include multifunctional acids such as triphenylhexanoic acid, or pyromellitic acid, or tris to hexavalent alcohols, methylolpropane, pentaerythritol, dipentaerythritol, glycerol, or phases Corresponding hydroxide. According to the present invention, PBT and / or PTMT is mixed with 0.05 to 2.5% by weight of the added polymer as an extension enhancer. Additive polymers that are particularly useful for this purpose of the present invention include the following specific polymers or copolymers: 1. Polymers are polymerized from monomers, the general formula of which is as follows 1237670 _ Description of the invention continued page
其中R1及R2是替代物,包含選項的原子C、Η、Ο 、S、Ρ及鹵素原子,R1及R2的分子量總合最少是 40。單體的範例有丙稀酸、甲基丙烯酸、及CH2= CR-COOR’,其中R是Η原子或CH3群,而R,是 Ci_i5院基、或C5-I2環院基、或C6-14方香基、苯乙 烯、及Cy甲基取代的苯乙烯。 2. 含下列單體的共聚物 A =丙稀酸、甲基丙烯酸、及CH2=CR-COOR’,其 中R是Η原子或CH3群,而R’是Ci_15院基、 或C5-12〗哀院基、或C6-14方香基。Among them, R1 and R2 are substitutes, including optional atoms C, Η, Ο, S, P, and halogen atoms, and the total molecular weight of R1 and R2 is at least 40. Examples of monomers are acrylic acid, methacrylic acid, and CH2 = CR-COOR ', where R is a fluorene atom or a CH3 group, and R is a Ci_i5 radical, or a C5-I2 circular radical, or C6-14 Allyl, styrene, and Cy methyl-substituted styrene. 2. Copolymers containing the following monomers: A = acrylic acid, methacrylic acid, and CH2 = CR-COOR ', where R is a fluorene atom or a CH3 group, and R' is a Ci_15 compound, or C5-12. Yuanji, or C6-14 Fang Xiangji.
B =苯乙烯、及C i _3甲基取代的苯乙嫌。 共聚體含60到98重量%A,2到40重量, 比較偏好是83到98重量及2到17重量%B, 而更好的是90到98重量%A及2到15重量%的 B (總合爲100重量% )。 3. 含下列單體的共聚物B = styrene and C i _ 3 methyl substituted styrene. The interpolymer contains 60 to 98% by weight A, 2 to 40% by weight, with preferences of 83 to 98% by weight and 2 to 17% by weight B, and more preferably 90 to 98% by weight A and 2 to 15% by weight B ( The total is 100% by weight). 3. Copolymers containing
C =苯乙嫌、及C i _3甲基取代的苯乙烯。 d =下列方程式π、m或IV的1或多個單體。 14 1237670 _ 發明說明續頁C = styrene, and Ci_3 methyl substituted styrene. d = 1 or more monomers of the following equation π, m or IV. 14 1237670 _ Description of the invention continued
其中R3、R4、R5每個都是Η原子、或<^_15烷 基、或C5_12環院基、或 C6-14 芳香基。 共聚體含15到95重量%的C,及2到80重量% 的D,比較偏好是50到90重量%的C及10-50重 量%的D,而更偏好的是70到85重量%的C及15 到30重量%的D。C與D的總合爲100重量%。 4.共聚物,含以下單體單元Among them, R3, R4, and R5 are each a fluorene atom, or a <^ _ 15 alkyl group, or a C5-12 ring group, or a C6-14 aromatic group. The interpolymer contains 15 to 95% by weight of C and 2 to 80% by weight of D. Preferred is 50 to 90% by weight of C and 10-50% by weight of D, and more preferred is 70 to 85% by weight of C. C and 15 to 30% by weight of D. The total of C and D is 100% by weight. 4. Copolymer, containing the following monomer units
E =丙稀酸、丙酸或CH2=CR-COOR’,其中R是Η 原子或CH3群,R’是(^_15烷基、或C5_12環烷 基、或C6_14芳香基。 F =苯乙烯或Ci_3院基取代的苯乙嫌。 g =下列方程式π、m或IV的1或多個單體。E = acrylic acid, propionic acid or CH2 = CR-COOR ', where R is a fluorene atom or a CH3 group, and R' is a (^ _15 alkyl group, or a C5_12 cycloalkyl group, or a C6_14 aromatic group. F = styrene or Ci_3 is substituted by phenyl ethyl. G = 1 or more monomers of the following formula π, m or IV.
15 1237670 _ 發明說明續頁 其中R3、R4、R5每個都是Η原子、或(^_15烷 基、或〔5·12Ϊ哀院基、或C6-14方香基。 η = 1個或多個乙烯非飽和單體,可以與下列Ε、F 、或/及G共聚合,此係由以下的群組選擇: 包括甲基苯乙烯、乙酸乙嫌酯、丙烯酸酯、甲 基丙稀酯,除了 Ε以外,丙稀、丙稀醯胺、氯 乙烯、乙烯叉二氯、鹵素取代的苯乙烯、乙烯 醚、異丙醚及二烯。 此共聚合物包含30到90重量%的Ε ’ 〇到50重量 %的F,> 〇到50重量%的G,以及0到50重量 %的Η。比較偏好的是45到97重量%的Ε,0到 30重量%的F,3到40重量%的G,以及〇到30 重量%的Η。以及更偏好的是60到94重量%的Ε ,0到20重量%的F,6到3〇重量%的G,以及0 到20重量%的Η。Ε、F、G與Η的總合爲100重 量%。 成分Η是選項。本發明的優點本可以由包含成分Ε到 G的共聚物達成,但依據本發明,其優點也可以由使用Η 成分的單體建構共聚物達成。 依據本發明,較偏好選用成分Η,此對所要使用的共 聚物不會有負面影響。 成分Η也可用來修改共聚物的物性至希望的型式,例 如,增加或改良加熱到溶融温度時共聚物的流體性質、減 少共聚物的殘餘顏色、或使用多功能單體使共聚物具有一 16 1237670 _一 發明說明續貢 些交聯(CROSSLINKING)的f生會g。 爲了這些理由,也可以選用成分Η來增強成分E至G 單體的共聚性能,例如ΜΑ及ΜΜΑ,它們本來不能共聚 ,但是有第三成分加入時,如苯乙烯,就會開始共聚。15 1237670 _ Description of the invention Continuation page where R3, R4, and R5 are each a fluorene atom, or (^ _15 alkyl, or [5 · 12 fluorene group, or C6-14 scent group. Η = 1 or more ethylene Unsaturated monomers can be copolymerized with the following E, F, or / and G, this is selected by the following groups: including methylstyrene, ethyl acetate, acrylate, methyl propylene, except for Ε In addition, propylene, chloramine, vinyl chloride, vinylidene chloride, halogen-substituted styrene, vinyl ether, isopropyl ether, and diene. This copolymer contains 30 to 90% by weight of E ′ 〇 to 50 F% by weight,> 0 to 50% by weight G, and 0 to 50% by weight rhenium. Preferred are 45 to 97% by weight E, 0 to 30% by weight F, and 3 to 40% by weight. G, and 0 to 30% by weight of rhenium. And more preferred are 60 to 94% by weight of E, 0 to 20% by weight of F, 6 to 30% by weight of G, and 0 to 20% by weight of rhenium. The total of E, F, G and Η is 100% by weight. Component Η is an option. The advantages of the present invention could have been achieved by a copolymer containing components E to G, but according to the present invention, its advantages The point can also be achieved by using a monomer to construct a copolymer of the Η component. According to the present invention, the component Η is preferred, which does not have a negative impact on the copolymer to be used. The component Η can also be used to modify the physical properties of the copolymer to the hope Type, for example, increase or improve the fluid properties of the copolymer when heated to the melting temperature, reduce the residual color of the copolymer, or use the multifunctional monomer to make the copolymer have a 16 1237670 _ An invention description continued to cross link (CROSSLINKING For these reasons, component Η can also be selected to enhance the copolymerization performance of components E to G monomers, such as MA and MMA, which could not be copolymerized, but when a third component is added, such as styrene, Will begin to copolymerize.
符合這個目的的有用單體包括乙烯酯、丙稀酸酯’例 如丙烯酸甲酯、及丙烯酸乙酯、異丁烯酸甲酯以外的甲基 丙烯酸酯,例如甲基丙烯酸丁酯、及乙己酸甲基丙烯酸酯 、丙稀、丙稀醯胺、甲基丙稀醯胺、氯乙烯、乙烯叉二氯 、苯乙烯、甲基苯乙烯、及各種的鹵素取代的苯乙烯、乙 烯醚、乙醚異丙烯酯、二烯,例如1,3 丁二烯及二乙烯基 苯。要降低共聚物顏色最好是使用多電子單體,例如乙烯 醚、乙酸乙烯酯、苯乙烯、或甲基苯乙烯。 成分Η中最好的化合物是芳香乙烯基單體,例如苯乙 烯、或甲基苯乙烯。Useful monomers suitable for this purpose include vinyl esters, acrylic esters such as methyl acrylate, and ethyl acrylates, methacrylates other than methyl methacrylate, such as butyl methacrylate, and ethanoic acid methacrylic acid Esters, propylene, acrylamide, methacrylamide, vinyl chloride, vinylidene chloride, styrene, methylstyrene, and various halogen-substituted styrenes, vinyl ethers, ether isopropenyl esters, Diene, such as 1,3 butadiene and divinylbenzene. To reduce the color of the copolymer, it is preferable to use a multi-electron monomer such as vinyl ether, vinyl acetate, styrene, or methylstyrene. The best compound in ingredient VII is an aromatic vinyl monomer such as styrene or methylstyrene.
熟悉此技術的人都知道上述聚合物或共聚物的生產方 法。此在WO 99/07297中有詳細記載。 本發明特別偏好使用珠粒形的添加劑聚合物及/或共 聚物,其顆粒大小在特別有利的範圍內。依據本發明使用 的添加聚合物及/或共聚物,如將其與纖維聚合物熔漿混 合時,以顆粒形態最爲有利,其平均直徑在〇.〇1到1.0mm 之間。但是,也可以用較大或較小的珠子或碎片。添加聚 合物及/或共聚物也可以已經涵含在聚合物混合物的碎片 內,而免定量添加之煩。 本發明亦偏好添加無定形且不能溶解的添加聚合物及 17 1237670 _ 發明說明續頁 /或共聚物於聚酯混合物內。它們最好是玻璃轉換溫度在 90 - 200°C。其玻璃轉換溫度可用習知方法測知。最好是 用分掃瞄量熱法。詳如WO 99/07927所載。 選擇添加聚合物及/或共聚物,最好是添加聚合物及 /或共聚物與聚合物混合物的熔漿黏度比例在〇.8: 1到 10 : 1之間◦如在1.5 : 1到8 : 1之間者則更理想。熔漿 黏度可用習知的方法測知,例如用振動電流計,其振動頻 率在2.4HZ,溫度是聚合物混合物的熔點加28t:。PTMT 的熔漿黏度的溫度是255°C。詳如WO 99/07927記載。 添加聚合物及/或共聚物的熔漿黏度最好高於聚合物混合 物的熔漿黏度。又選擇添加聚合物及/或共聚物的黏度範 圍及選擇與聚合物混合物的黏度比例有助於紗製品的品質 臻於完善,黏度比例如屬理想,必能降低添加聚合物及/ 或共聚物的用量。從而能增進製法的經濟效益。聚合物摻 合物在旋轉紡絲前最好含〇.〇5到2.5重量%的添加聚合物 及/或共聚物,其添加量在〇·25到2.0重量%則更爲理想 〇 選擇有利的黏度比例提供添加聚合物及/或共聚物在 聚合物混合物內狹窄的顆粒大小分布同時在纖維中需要的 添加聚合物及/或共聚物的小纖維結構。添加聚合物及/ 或共聚物比聚合物混合物高的玻璃轉換溫度就是保證在旋 轉成型纖維中的小纖維結構的快速整合◦由妨織突起器出 來的添加聚合物及/或共聚物的最大顆粒大小約是1000nm ◦而平均顆粒大小是小於400nm。最有利的小纖維結構是 18 1237670 ____ 發明說明續頁 在纖維抽出後得到。其時細絲含有最少60重量%小纖維 型態的添加聚合物及/或共聚物’長度在〇·5到20um之 間,而直徑是0.01到0.5um。 本發明有用的聚酯最好是可以熱成型的塑膠’而且能 旋轉成型到細絲並且纏繞。在這裏’特別有利的聚醋黏度 限在 0.70dl/g 到 〇.95dl/g 之間。 聚合物熔漿要直接來自由聚凝結工廠的最後反應槽或 由瑢漿擠壓成型機生產的固體聚合物片。 一個已知的整合旋轉成型添加物的方法是在熔融或固 體狀態下量測進入聚合物混合物然後均勻分散形成細顆粒 。最好是使用DE 10022889所示的裝置。 本發明的製法並不限於任一特定的旋轉抽絲成型方法 。相反的所有的傳統旋轉抽絲成型製程都可以使用。因此 ,雖然在此討論一非常特別的旋轉抽絲成型製法,但也參 考一般技術知識,特別是FOURNE ( 1995 )所著 ''合成纖 維,,由慕尼黑HANSER出版。 在本發明喜好的具體製法中,聚酯的熔漿或其熔融混 合物經由旋轉抽絲成型幫浦以固定速度,此係用已知的方 程式算出可以得到需要的纖維線性密度的速度,打到紡織 突起機,然後經過壓鑄板中的孔擠壓成爲熔融細絲。 例如,熔漿可以在擠壓成型機中由聚合物片作成,這 時,首先將片乾燥到其含水量低於30ppm,最好是低於15 ppm 〇 熔漿的溫度,通常稱爲旋轉抽絲成型溫度而且是在旋 19 1237670 發明說明續頁 轉抽絲成型幫浦上量測,此是依據所使用的聚合物或聚合 物混合物的熔點而定。最好是在方程式i所提示的範圍內 方程式1Those skilled in the art are aware of the methods of producing the polymers or copolymers described above. This is described in detail in WO 99/07297. The present invention particularly favors the use of bead-shaped additive polymers and / or copolymers whose particle size is within a particularly advantageous range. The added polymers and / or copolymers used in accordance with the present invention are most advantageous in the form of particles when they are mixed with fiber polymer melts, and their average diameter is between 0.01 and 1.0 mm. However, larger or smaller beads or fragments can also be used. Adding polymers and / or copolymers can also be contained in the fragments of the polymer mixture without the trouble of quantitative addition. The present invention also favors the addition of amorphous and insoluble added polymers and 17 1237670 _ Description of the invention continued on page / or copolymer in a polyester blend. They preferably have a glass transition temperature of 90-200 ° C. Its glass transition temperature can be measured by conventional methods. It is best to use sub-scan calorimetry. Details are set out in WO 99/07927. Choose to add polymers and / or copolymers, it is best to add polymers and / or copolymers to polymer mixtures with a viscosity ratio of 0.8: 1 to 10: 1 such as 1.5: 1 to 8 : 1 is more ideal. The viscosity of the melt can be measured by conventional methods. For example, using a vibration galvanometer, the vibration frequency is 2.4HZ, and the temperature is the melting point of the polymer mixture plus 28t :. PTMT has a melt viscosity of 255 ° C. Details are described in WO 99/07927. The viscosity of the slurry with the added polymer and / or copolymer is preferably higher than the viscosity of the polymer mixture. In addition, the viscosity range and the viscosity ratio of the polymer and / or copolymer are selected to help improve the quality of the yarn product. For example, the viscosity ratio is ideal, and the polymer and / or copolymer can be reduced. The amount. Thereby, the economic benefits of the system can be enhanced. The polymer blend preferably contains 0.05 to 2.5% by weight of the added polymer and / or copolymer before spinning, and its addition amount is more preferably from 0.25 to 2.0% by weight. The viscosity ratio provides the narrow particle size distribution of the added polymer and / or copolymer in the polymer mixture while the small fiber structure of the added polymer and / or copolymer is required in the fiber. The higher glass transition temperature of the added polymer and / or copolymer than the polymer mixture is to ensure the rapid integration of the small fiber structure in the spin-formed fiber. The largest particle of the added polymer and / or copolymer from the weaving protrusion The size is about 1000nm and the average particle size is less than 400nm. The most advantageous small fiber structure is 18 1237670 ____ Description of the invention Continued page Obtained after fiber extraction. At this time, the filament contains at least 60% by weight of a small fiber type of the added polymer and / or copolymer 'having a length of 0.5 to 20 um and a diameter of 0.01 to 0.5 um. The polyester useful in the present invention is preferably a thermoformable plastic 'and can be spin-formed into filaments and wound. Here, the viscosity of poly (vinyl acetate) which is particularly advantageous is limited to between 0.70 dl / g and 0.95 dl / g. The polymer melt comes directly from the final reaction tank of the polycoagulation plant or from a solid polymer sheet produced by a pulp extrusion machine. A known method of integrating rotary molding additives is to measure into the polymer mixture in a molten or solid state and then uniformly disperse to form fine particles. The device shown in DE 10022889 is preferably used. The manufacturing method of the present invention is not limited to any particular spinning and drawing method. Conversely, all traditional spinning and drawing processes can be used. Therefore, although a very specific spinning spinning method is discussed here, reference is also made to general technical knowledge, in particular `` synthetic fibers, '' by FOURNE (1995), published by Munich Hanser. In the preferred specific manufacturing method of the present invention, the melt of polyester or its molten mixture is pumped at a fixed speed through a spinning drawing pump. This system uses a known equation to calculate the speed at which the linear density of the desired fiber can be obtained. The protrusion machine is then extruded through holes in the die-casting plate into molten filaments. For example, the melt can be made from polymer sheets in an extrusion molding machine. In this case, the sheet is first dried to a moisture content of less than 30 ppm, preferably less than 15 ppm. The temperature of the melt, usually referred to as spinning The molding temperature is also measured on the spin pump 19 1237670 Description of the Invention Continuing Spinning Molding Pump, which depends on the melting point of the polymer or polymer mixture used. Preferably within the range suggested by equation i Equation 1
Tm+ 15°C< Tsp < Tm+45〇C 其中Tm + 15 ° C < Tsp < Tm + 45〇C where
Tm=聚酯的熔點(°C )Tm = melting point of polyester (° C)
Tsp =旋轉抽絲成型溫度(°c ) 上開參數用來限制水解及/或熱黏度退化,越低越好 。依據本發明,黏度退化要低於〇.12dl/g,尤其最好是低 於 0.08dl/g。 熔漿均勻度會直接的影響旋轉抽絲成型細絲的材料特 質。除了在產品管線中的靜態混合器,最好再用最少有一 個元件的靜態混合器在旋轉抽絲成型幫浦下來將熔漿均勻 化。 壓鑄板溫度,此係依據旋轉抽絲成型溫度而定,由板 的二次加熱系統控制。可用的二次加熱系統包括用''DIPHY "加熱的旋轉樑,或附加的對流或輻射加熱器。一般來說 壓鑄板溫度與旋轉抽絲成型溫度向來是相同的。Tsp = Rotary wire drawing forming temperature (° c) The opening parameter is used to limit hydrolysis and / or thermal viscosity degradation, the lower the better. According to the present invention, the viscosity degradation is less than 0.12 dl / g, particularly preferably less than 0.08 dl / g. The uniformity of the slurry will directly affect the material properties of the spinning wire. In addition to the static mixer in the product line, it is best to use a static mixer with a minimum of one component to homogenize the melt under the spinning wire drawing pump. The temperature of the die-casting plate is determined by the temperature of the spinning wire drawing and is controlled by the secondary heating system of the plate. Available secondary heating systems include rotating beams heated with `` DIPHY '', or additional convection or radiant heaters. Generally, the temperature of the die-casting plate and the spinning drawing temperature are always the same.
經由紡織突起機的壓力升降率可以增加壓鑄板的溫度 。此方面的文獻有Κ. RIGGERT所著''FORTSHRITTE IN DER HERSTELLUNG VON POLYSTER-REIFENKORDGARN ,,,CHEMIEFASERN,21 版,379 頁(1971 ),據說壓力每 降低lOObar,溫度增加約4°C 20 1237670 _ 發明說明續頁 也可以經由過濾器媒介物來控制壓鑄板壓力,特別是 用鋼砂,其平均顆粒在O.iO到l.2mm之間,最好是0.12 到0.75mm及/或過濾盤。此可由針織或非針織金屬纖維 製成,細度爲S40um。The temperature of the die-casting plate can be increased by the pressure rise and fall rate of the textile protrusion machine. Literature in this regard includes `` FORTSHRITTE IN DER HERSTELLUNG VON POLYSTER-REIFENKORDGARN by K. RIGGERT, '', CHEMIEFASERN, 21 edition, 379 pages (1971). It is said that for every 100 bar pressure reduction, the temperature increases by about 4 ° C. Note that the continuation page can also control the pressure of the die-casting plate through the filter medium, especially the steel sand, whose average particle is between 0.1 to 1.2 mm, preferably 0.12 to 0.75 mm and / or the filter disk. This can be made of knitted or non-woven metal fibers with a fineness of S40um.
此外,壓鑄孔的壓力差也有助於總壓力。壓鑄的壓力 最好是設定在80bar與450bar之間’特別好是在1〇〇與 250bar 之間。 旋轉抽絲成型線伸長比例isp’就是取出速度與擠壓 成型速度比,是依據US 5250245所指方程式2,由聚合物 或聚合物混合物密度、紡織突起機孔直徑及細絲線性密度 計算而定。 方程式2 isp= 2.25 · 105 · ( d · P) · D2 ( cm) /Dpf ( den) 其中In addition, the pressure difference of the die-casting holes also contributes to the total pressure. The pressure of the die-casting is preferably set between 80 bar and 450 bar ', particularly preferably between 100 and 250 bar. The elongation ratio isp 'is the ratio of the take-off speed to the extrusion speed. It is based on the equation 2 of US 5250245. It is determined by the calculation of the density of the polymer or polymer mixture, the diameter of the hole of the textile protrusion and the linear density of the filament . Equation 2 isp = 2.25 · 105 · (d · P) · D2 (cm) / Dpf (den) where
d=熔漿密度(g/cm3),就 PTMT 而言,d=1.12g/cm3 D=紡織突起機孔直徑(cm)d = melt density (g / cm3), in terms of PTMT, d = 1.12g / cm3 D = diameter of textile protrusion machine hole (cm)
Dpf=每一細絲的 Denier (den) 爲了本發明的目的,旋轉抽絲成型線伸長比例最有利 是在70與500之間,特別好是在1〇〇與250之間。 紡織突起機孔的長度與直徑比例最好是選在i.5與6 之間,特別是1.5與4之間。 ^ 擠壓成型的細絲通過一冷卻延遲區。此冷卻延遲區位 於旋轉抽絲成型器正下方的凹陷區域,以保護由,妨織突起 機孔出來的細絲不被受到冷卻空氣直接的影響。此凹卩白區 21 1237670 _ 發明說明續頁 的主動部分是建造成由旋轉抽絲成型機到旋轉抽絲成型樑 間的延伸部份,因此細絲即被加熱的牆所包圍。被動部分 則由絕緣及沒有加熱的框架形成。主動部分最有利的長度 是在0到100mm,被動部分最有利的長度是在20到120 mm之間。最好的總長是30- 200mm之間,或30- 120mm 之間。 主動凹陷區的替代方案是將再熱器放在旋轉抽絲成型 樑下。與主動凹陷區不同的是此一區的圓柱或長方形的切 面包含最少一加熱的系統與旋轉抽絲成型樑各自獨立。 在放射性多孔冷卻系統,該系統係集中包圍著旋轉抽 絲成型線,冷卻延遲能用圓柱圍板達成。 細絲此後再冷卻到溫度低於固化溫度。本發明所用的 固化溫度是指熔漿由熔融進入固體狀態的溫度。 在本發明而言,當細絲冷卻到一它不再感覺黏著的溫 度時是最有利的。特別有利的是將細絲冷卻到溫度低於它 們的結晶溫度,特別是低於其玻璃轉換溫度。 冷卻細絲方法可在文獻中獲得。依據本發明,最有用 的是用冷卻氣體,尤其是冷空氣。冷卻空氣的溫度最好是 在12°C到35°C之間,特別是在16°C到26°C的範圍內。冷 卻空氣的最有利流速是在0.20m/sec到0.55m/sec的範圍。 細絲可以用單端冷卻系統包含有波浪牆的單一冷卻管 來冷卻。用主動的供應冷卻空氣或用細絲的自吸作用來冷 卻每一細絲。替代每一單獨的管,也可以用習用的交叉流 冷卻系統。 22 1237670 _ 發明說明續頁 及油入口孔的寬度須與紗的線性速度及細絲數量相符。孔 與寬度範圍是1.0mm到4.0mm最適合。油針的出口部分 的架構須劃一,最好能包含油槽在內。油槽可以向德國 CERAMTEC 或美國 GOULSTON 購得。 對本發明來說,均勻的使用油是最重要的。均勻能由 譬如使用ROSSA計來決定,詳如CHEMIEFASSERN/ TEXTILINDUSTRIE,42/94 1992_11 月,第 896 頁所載。 此法在提供使用油的標準偏差値小於90位數(DIGITS), 尤其是小於60位數。本發明特別需要使用油的標準偏差 値是小於45位數。尤其是小於30位數。標準偏差90或 45位數大槪相當於6.2%及3.1%變動係數。 對本發明特別有利的是設計旋轉抽絲成型完成線及幫 浦成自己去油,來避免發生氣泡,因爲氣泡會導致油使用 量有很大的變動。 依據本發明,特別需要在纏繞紗之前將細絲捲入。在 本發明內,能關閉紗管的噴嘴就特別適用,因爲此類系統 即使在低的紗張力及高空氣壓力時,會防止紗在進料槽打 結。捲入的噴嘴最好是放在滾筒之間。紗出口張力就由滾 筒的進及出的速度不同來控制。紗出口張力不得超過〇.2〇 cN/dtex,基本上應該在 〇.〇5cN/dtex 與 〇·ΐ5 cN/dtex 之間 。捲入的空氣壓力在0.5與5.5bar之間,或者,當取出速 度到3500m/min時,其壓力最多不超過3.0bar。 紗最好是捲入到節點數量最少爲1 Οη/m。最好是最大 的無節點空隙低於100cm與節點數量係數變動値低於1〇〇 24 1237670 _ 發明說明續頁 %。特別有利的是利用空氣壓力高於l.Obar來提高節點數 量到匕15n/m。其時特徵是高均勻度,如此變動係數就不 會超過70%,最大的無節點空隙會是50cm。在實際使用 上,德國TEMCO的LD系統、美國SLACK AND PARR或 HEBERLEIN的POLYJET都蠻好用的。 第一個滾筒的周行速度是稱爲取出速度。紗被纏繞前 ,在纏繞組合裏,可以使用更多的滾筒在管子上形成纏線 管,以此用來抽取、或熱定型及/或放鬆多絲紗。 在本發明所說的一個特別有用作法是在多絲紗纏繞前 先經過熱處理,溫度最好定在50到150°C,熱處理可用任 何一項習知的方法去做。最適合的熱處理方式是用加熱的 滾筒。爲這個目的所使用的滾筒包括FOURNE ( 1995 )所 著 ''合成纖維〃一書中所指的設備(由慕尼黑HANSER出 版)。 本發明還有一可用的作法,是對多絲紗用熱氣體作熱 處理,特別是熱空氣。 在本發明第三個想要的作法,是對多絲紗用輻射熱作 熱處理。 多絲紗的熱處理也可將紗接近但不接觸加熱的表面, 詳如EP 731196所載。 穩定無缺失的組合是無缺失纏繞紗及想做進一步無缺 失加工的基本要件。因此,依據本發明,有利的捲動張力 定在0.025cN/dtex—0.15cN/dtex,而最好的張力範圍是0.03 cN/dtex—0.08cN/dtex 之間。 25 1237670Dpf = Denier (den) for each filament For the purpose of the present invention, the elongation ratio of the spinning wire is most advantageously between 70 and 500, particularly preferably between 100 and 250. The ratio of the length and the diameter of the hole of the textile projection machine is preferably selected between i.5 and 6, especially between 1.5 and 4. ^ Extruded filaments pass through a cooling delay zone. This cooling delay zone is located in a recessed area directly below the rotary wire drawing molder to protect the filaments from the holes of the weaving protrusions from being directly affected by the cooling air. This recessed white area 21 1237670 _ Description of the Invention The active part of the continuation sheet is constructed as an extension from the rotary spinning machine to the rotary spinning beam, so the filaments are surrounded by the heated wall. The passive part is formed by an insulated and unheated frame. The most advantageous length of the active part is between 0 and 100 mm, and the most advantageous length of the passive part is between 20 and 120 mm. The best overall length is between 30-200mm, or between 30-120mm. An alternative to actively recessed areas is to place the reheater under a spinning wire-forming beam. Different from the active recessed area, the cylindrical or rectangular cross section of this area contains at least one heating system and the spinning wire drawing beam is independent of each other. In a radioactive porous cooling system, which is a system that surrounds a rotary wire drawing line, the cooling delay can be achieved with a cylindrical enclosure. The filaments are thereafter cooled to a temperature below the curing temperature. The curing temperature used in the present invention refers to the temperature at which the molten slurry enters a solid state from melting. For the purposes of the present invention, it is most advantageous when the filament is cooled to a temperature where it no longer feels sticky. It is particularly advantageous to cool the filaments to a temperature below their crystallization temperature, especially below their glass transition temperature. Cooled filament methods are available in the literature. According to the present invention, it is most useful to use a cooling gas, especially cold air. The temperature of the cooling air is preferably between 12 ° C and 35 ° C, especially in the range of 16 ° C to 26 ° C. The most favorable flow rate of the cooling air is in the range of 0.20 m / sec to 0.55 m / sec. The filaments can be cooled with a single cooling tube containing a wave wall in a single-ended cooling system. Each filament is cooled by actively supplying cooling air or by the self-priming action of the filament. Instead of each individual tube, a conventional cross-flow cooling system can also be used. 22 1237670 _ Description of the invention Continued and the width of the oil inlet hole must match the linear speed of the yarn and the number of filaments. The hole and width range is most suitable for 1.0mm to 4.0mm. The structure of the outlet part of the oil needle must be uniform, and it is better to include the oil groove. Oil tanks are available from CERAMTEC, Germany or GOULSTON, USA. For the present invention, the uniform use of oil is the most important. Uniformity can be determined, for example, using a ROSSA meter, as detailed in CHEMIEFASSERN / TEXTILINDUSTRIE, 42/94 1992_November, page 896. This method provides the standard deviation of the used oil 値 less than 90 digits (DIGITS), especially less than 60 digits. The present invention particularly requires the standard deviation 使用 of the oil to be used to be less than 45 digits. Especially less than 30 digits. Standard deviations of 90 or 45 digits are equivalent to 6.2% and 3.1% coefficients of variation. It is particularly advantageous for the present invention to design the rotary wire drawing forming completion line and to help the oil remove oil by itself to avoid air bubbles, because air bubbles can cause large changes in the amount of oil used. According to the invention, it is particularly necessary to wind the filament before winding the yarn. In the present invention, the nozzle capable of closing the bobbin is particularly suitable because such a system prevents the yarn from kinking in the feed slot even at low yarn tension and high air pressure. The wound nozzle is preferably placed between the rollers. The yarn exit tension is controlled by the different speeds of the roller in and out. Yarn exit tension should not exceed 0.20 cN / dtex, which should basically be between 0.05cN / dtex and 0.5cN / dtex. The pressure of the entrained air is between 0.5 and 5.5 bar, or when the take-off speed reaches 3500 m / min, the pressure does not exceed 3.0 bar at most. The yarn is preferably wound up to a minimum of 10 η / m. It is best if the maximum no-node gap is less than 100cm and the variation of the number of nodes coefficient is less than 10024 1237670 _ Description of the invention continued on%. It is particularly advantageous to use air pressure higher than 1.0 bar to increase the number of nodes to 15 n / m. At that time, it was characterized by high uniformity, so that the coefficient of variation would not exceed 70%, and the maximum no-node gap would be 50 cm. In practice, the LD system of German TEMCO, SLACK AND PARR of the United States, or POLYJET of HEBERLEIN are all very good. The peripheral speed of the first drum is called the take-out speed. Before the yarn is wound, in the winding combination, more rollers can be used to form a winding tube on the tube, which can be used to extract, heat set and / or relax the multi-filament yarn. A particularly useful method in the present invention is to heat-treat the multifilament yarn before winding it, preferably at a temperature of 50 to 150 ° C. The heat-treatment can be performed by any conventional method. The most suitable heat treatment is a heated roller. Drums used for this purpose include the equipment referred to in the book '' Synthetic Fibre '' by FOURNE (1995) (published by HANSER, Munich). Another useful method of the present invention is to heat the multifilament yarn with hot gas, especially hot air. A third desirable method in the present invention is to heat treat the multifilament yarn by radiant heat. Heat treatment of multifilament yarns can also bring the yarns close to but not in contact with the heated surface, as described in EP 731196. A stable and missing-free combination is a basic element for missing-free winding yarns and for further defect-free processing. Therefore, according to the present invention, the advantageous rolling tension is set to 0.025 cN / dtex to 0.15 cN / dtex, and the best tension range is 0.03 cN / dtex to 0.08 cN / dtex. 25 1237670
依據本發明,有一項重要的處理參數是在取出滾筒上 及滾筒間的紗張力設定。基本上這張力是由HAMANA的 真正定向張力、以及紗引導的摩擦張力油針與紗空氣的摩 擦張力組合而成。爲了本發明的目的,在取出滾筒上及其 間的紗張力是定在〇.〇5cN/dtex到0.20cN/dtex之間,最好 是在 0.08cN/dtex 到 〇.15cN/dtex 之間。 過低的張力,如低於〇.〇5cN/dtex,將不能提供所需要 的部分定向程度。但當張力超過0.20cN/dtex時,此張力 常會在纏繞及儲存紗管時引發記憶效應問題而使紗的參數 退化。 依據本發明,張力是由紡織突起機噴嘴與油機間的距 離、摩擦表面以及油機與取出滾筒間的距離控制的。有利 的長度是不超過6.0米,最好是小於2.0米。此因旋轉抽 絲成型系統及取出機組是用平行配置來確保紗的行進成一 直線所致。 幾何參數也足以釋明紗在輸送點與捲動點之間的調節 時間。在這段時間內的快速放鬆會有影響紗包品質的效果 。所謂調節時間最好是選擇在50到200ms之間。 依據本發明,預定向紗的捲動速度定在2200m/min與 6000m/min之間。最好是選擇捲動速度在2500m/min與 6000m/min之間。此對聚合物混合物的纏繞速度在3500 m/min與6000m/min之間者特別有利。 依據本發明,纏繞後的多聚酯紗包的熱處理溫度是在 > 45°C到65。(:之間。熱處理的時間可以自由選擇。但是如 26 1237670 _ 發明說明續頁 用習知的方法,例如加熱滾筒或熱軌,其處理的時間自然 的會長很多。依據本發明,在前述的溫度範圍的熱處理最 少需5分鐘,最好是不少於10分鐘,更好是不少於20分 鐘,特別好的是30分鐘或以上。以上的時間係自纏繞開 始算起。 也可以用任何習知的方式做熱處理。適當的方法包含 熱傳導、熱對流及/或熱輻射原理。本發明比較喜歡使用 的方法是,將纏繞的紗包用加熱的捲或滾筒作熱處理,最 好是使用最少一個接觸面的滾筒,而且同時還可量測與控 制纏繞速度。本發明更比較喜歡使用的方法是,將纏繞的 紗包用輻射熱處理。 本發明第三個喜歡使用的方法是,將纏繞的紗包用加 熱的氣體作熱處理。適當的氣體包括空氣與惰性氣體,如 氮、氦及/或氬。在本文,使用熱空氣已被認定是最好的 方法。熱氣的溫度最好是能與在箱體內的溫度一致,即> 45t到65°C。因此熱空氣的溫度範圍最好是>45°C到65°C 。從而熱氣的相對濕度最好是在40到90%之間。熱氣在 入口的流速最好是5到100m3/h範圍內。 纏繞後紗包的熱處理最好是用一種裝置來纏繞一或多 條的多絲紗,此包括一箱體及一可旋轉的紡錘,蓋可將管 固定在其上而使管被箱體包住。熱處理最好是在箱體中執 行,最好是用熱傳導、熱對流及/或熱輻射加熱纏繞紗包 〇 旋轉紡錘是繞線機的一部份。最少要有一個管是夾在 27 1237670 _ 發明說明 旋轉紐鍾的夾頭上。而且最少要有一個多絲紗纏繞到最少 一支管上形成最少一纏繞紗包。在纏繞後,最少要有一支 管,帶著纏繞紗包,能由夾頭上移除。 任何種類以前使用過的繞線機都可以用在本發明,只 要能達成本發明的目的。關於進一步的細節,請參閱技術 文獻,特別是FOURNE ( 1995 )的書、'合成纖維〃由慕尼 黑HANSER出版。現有的繞線機技術如同傳統的一樣,本 發明允許同時在一紡錘上纏繞1或多條,特別是1到12條 多絲紗。依據本發明,最好同時纏繞多條多絲紗來增加旋 轉抽絲成型作業的效率。 纏繞1或多條多絲紗裝置的箱體可以用任何習知的材 料製造。但是,最有利的是使用熱絕緣材料,更好是也能 絕緣噪音。適當的材料包括塑膠,特別是有玻璃轉換溫度 大於65°C的塑膠、金屬,例如不鏽鋼與合金。熱絕緣材料 可以用單層結構或多層結構的,如2、3或更多層。最好 是,熱絕緣材料的熱傳導係數是小於10w/(m · k),最好的 是小於1 w/(m · k),更好是大於0·5 w/(m · k),最最好是 大於0.1 w/(m.k)。當使用三層熱絕緣與噪音絕緣材料時 其中間層材料的熱傳導係數要小於0·1 w/(m · k),而外層 材料最好是包括金屬或合金,或者是由金屬或合金組成的 ’此會得到特別有利的結果。 相體的大小最好是在其中能安放全部繞線機或者是至 少能安放夾頭及最大直徑的紗管包含纏繞紗包在內。最有 利的箱體還要能安放額外的纏繞設備,包括接觸滾筒來控 28According to the invention, an important processing parameter is the setting of the yarn tension on the take-out drum and between the drums. Basically, this tension is the combination of the true directional tension of HAMANA and the friction tension of the yarn-guided friction needle and yarn air. For the purpose of the present invention, the yarn tension on and between the take-out drum is set to be between 0.05 cN / dtex and 0.20 cN / dtex, preferably between 0.08 cN / dtex and 0.15 cN / dtex. Too low tension, such as below 0.05 cN / dtex, will not provide the required degree of partial orientation. However, when the tension exceeds 0.20cN / dtex, this tension often causes memory effect problems during winding and storage of the bobbin and degrades the yarn parameters. According to the present invention, the tension is controlled by the distance between the nozzle of the textile protrusion machine and the oil machine, the friction surface, and the distance between the oil machine and the take-out drum. An advantageous length is not more than 6.0 meters, preferably less than 2.0 meters. This is due to the fact that the spinning and drawing system and the take-out unit are arranged in parallel to ensure that the yarn travels in a straight line. The geometric parameters are sufficient to explain the adjustment time of the yarn between the conveying point and the rolling point. Quick relaxation during this time will affect the quality of the yarn package. The so-called adjustment time is preferably selected between 50 and 200ms. According to the invention, the winding speed of the predetermined yarn is set between 2200 m / min and 6000 m / min. It is best to choose a scroll speed between 2500m / min and 6000m / min. This is particularly advantageous for winding speeds of polymer mixtures between 3500 m / min and 6000 m / min. According to the present invention, the heat treatment temperature of the wound multi-polyester yarn package is > 45 ° C to 65 °. (: Between. The time for heat treatment can be freely selected. However, such as 26 1237670 _ Description of the Invention Continued pages use conventional methods, such as heating rollers or hot rails, the processing time will naturally be much longer. According to the present invention, in the aforementioned The heat treatment in the temperature range takes at least 5 minutes, preferably not less than 10 minutes, more preferably not less than 20 minutes, and particularly preferably 30 minutes or more. The above time is calculated from the start of winding. Anything can be used Heat treatment in a conventional manner. Suitable methods include the principles of heat conduction, convection, and / or heat radiation. The preferred method of the present invention is to heat the wound gauze with a heated roll or drum, preferably with a minimum of A contact surface roller can measure and control the winding speed at the same time. The more preferred method of the present invention is to heat the wound gauze with radiation. The third preferred method of the present invention is to wind the The yarn wrap is heat treated with a heated gas. Suitable gases include air and inert gases such as nitrogen, helium, and / or argon. Here, hot air has been used. It is considered to be the best method. The temperature of the hot air is preferably consistent with the temperature in the cabinet, that is,> 45t to 65 ° C. Therefore, the temperature of the hot air is preferably> 45 ° C to 65 ° C. Therefore, the relative humidity of the hot air is preferably between 40 and 90%. The flow rate of the hot air at the inlet is preferably in the range of 5 to 100 m3 / h. The heat treatment of the wrapped yarn bag is preferably wound with one or more devices. The multi-filament yarn includes a box body and a rotatable spindle, and the cover can fix the tube to the tube so that the tube is covered by the box body. The heat treatment is preferably performed in the box body, preferably by heat conduction, Thermal convection and / or thermal radiation heat the wrapped yarn package. Rotary spindle is part of the winding machine. At least one tube is clamped on 27 1237670 _ Description of the invention Rotary knobs. And at least one multi-filament The yarn is wound on at least one tube to form at least one winding gauze. After winding, at least one tube with the winding gauze can be removed from the chuck. Any kind of previously used winding machine can be used in this machine. Invention, as long as the purpose of the invention can be achieved. For details of the steps, please refer to the technical literature, especially the book by FOURNE (1995), 'Synthetic Fibers' published by HANSER in Munich. The existing winding machine technology is as traditional, and the present invention allows to wind 1 or more on a spindle at the same time. Strips, especially 1 to 12 multi-filament yarns. According to the present invention, it is best to wind multiple multi-filament yarns at the same time to increase the efficiency of the spin-drawing molding operation. It is made of conventional materials. However, it is most advantageous to use thermal insulation materials, and it is also better to insulate noise. Suitable materials include plastics, especially plastics and metals with a glass transition temperature greater than 65 ° C, such as stainless steel and alloys. The thermal insulation material can use a single layer structure or a multilayer structure, such as 2, 3 or more layers. Preferably, the thermal conductivity of the thermal insulation material is less than 10 w / (m · k), more preferably less than 1 w / (m · k), and more preferably greater than 0 · 5 w / (m · k). It is preferably greater than 0.1 w / (mk). When using three layers of thermal insulation and noise insulation materials, the thermal conductivity of the intermediate layer material should be less than 0 · 1 w / (m · k), and the outer layer material preferably includes a metal or alloy, or consists of a metal or alloy 'This will give particularly favorable results. The size of the phase body is preferably such that it can house all the winding machines or at least the chuck and the largest diameter bobbin including the wrapped yarn package. The most profitable case is also to accommodate additional winding equipment, including contact rollers for control.
1237670 制績繞速度以及最好是一穿越裝置。是故最小的箱體要能 獲致高品負紗的無缺失的纏繞加工效果。 此外,也是同樣重要的是箱體的尺寸要最小,因此在 箱體外的纏繞室也要具備標準的作業條件,同時遂目b達成 箱體內部加熱的費用降到最低,箱體內最好是能用簡單^ 法送入多絲紗並要纏繞後的紗包容易移除,以及能生產尚 重量,最好是大於2公斤,更好是大於4公斤的_繞紗包 f 等目的。 本發明特別喜歡的方式是,纏繞後的紗包的熱處理是 - 在箱體內採用至少一種熱氣。這些氣體最好是由一個入口 · 進入箱體,然後由一個出口排出。最有利的是進出口連結 一起使氣體能在一包括有進口與出口的循環系統裡循環。 - 氣體,依紗移動方向來看,最好是將氣體送入到管子後方 ,再由管子前方排出。雖然氣體也可在箱體內加熱,不過 ,能在箱體外加熱俾使箱體內的溫度經常保持一致則更好1237670 A winding speed and preferably a crossing device. Therefore, the smallest box should be able to obtain the high-quality negative yarn without missing winding effect. In addition, it is also important that the size of the box is the smallest, so the winding room outside the box must also have standard operating conditions, and at the same time, the goal of achieving the minimum heating cost inside the box is best The yarn package that is fed into the multi-filament yarn by a simple method is easy to remove, and can produce still weight, preferably greater than 2 kg, and more preferably greater than 4 kg. A particularly preferred method of the present invention is that the heat treatment of the wrapped yarn package is-using at least one kind of hot gas in the box. These gases preferably enter the cabinet through an inlet, and then exit through an outlet. The most advantageous is that the inlet and outlet connections together allow gas to circulate in a circulation system that includes an inlet and an outlet. -According to the moving direction of the yarn, it is best to send the gas to the back of the tube and then discharge it from the front of the tube. Although the gas can also be heated inside the box, it is better to be able to heat it outside the box so that the temperature inside the box is often consistent.
依據本發明,箱體內溫度的量測最好是由至少一個溫 度感知器來做。而且氣體的溫度還能適當的在箱體外加熱 ,如此箱體內部的溫度才能保持在>45°C到65X:之間。此 外溫度感知器與氣體加熱元件最好是互相連結,如此才能 使氣體的溫度保持在一預先設定的範圍,最好的範圍是在 >45°C 到 65°C 之間。 本發明特別偏好的方法是對纏繞後紗包的熱處理,最 少要由一種熱的氣體在箱體內做成。該氣體最好是由一入 29 1237670According to the present invention, the temperature measurement in the cabinet is preferably performed by at least one temperature sensor. In addition, the temperature of the gas can be properly heated outside the cabinet, so that the temperature inside the cabinet can be maintained between > 45 ° C and 65X :. In addition, the external temperature sensor and the gas heating element are preferably connected to each other so that the temperature of the gas can be maintained in a preset range, and the best range is between > 45 ° C and 65 ° C. A particularly preferred method of the present invention is the heat treatment of the wrapped yarn package, at least made of a hot gas in the case. The gas is best made by a 29 2937670
口進入箱體,然後由一個出口排出。最好的是進出口連結 起來,俾氣體能在一循環系統循環。氣體,依紗移動的方 向來看,要先進入管子後方,然後由管子前方排出。雖然 氣體也能在箱體內加熱,但是最好還是在箱體外加熱以保 持箱體內溫度的均勻分佈。 依據本發明,箱體內溫度的量測最好是由一組以上的 溫度感知器來做。氣體的溫度爲求一致,最好是在箱體外 面予以適度加熱,而箱體內部的溫度要定在>45°C到65°C 。溫度感知窃:及氣體加熱兀件最好是互相連結,如此才能 使氣體的溫度控制在一預先設定的範圍內,最好的是在> 45°C到65°C之間。 在箱體內量測溫度之時,要與預設的値比較,然後依 據溫差,對加熱的氣體酌予加熱或降低或維持其溫度。俾 使箱體內的溫度能保持在所需要的範圍內。 箱體內溫度要在至少二個點上測試。依紗移動的方向 來看,最好是在套筒前及套筒後檢查其箱體內的溫度是否 經常一致。還要適度調整氣體溫度及其流量以防溫度的變 異。 爲便在開始纏繞前送入多絲紗,箱體最好是有一開口 。特別是槽溝形的開口。槽溝的配置,依紗移動的方向來 看,多絲紗最好是橫向的進入箱體。在纏繞時,槽溝要部 分的用適當的方法蓋住,使箱體內部與外間絕緣,以避免 一 在相體內的溫度發生差異。在本發明特別偏好的方法是, 厂’了: 覆蓋的方式是使用翼片,使它固定在箱體的外表面,在旋 广八.1 30 發明_月續頁 轉抽絲及纏繞時 時開啓。此翼片铲如^刀的鸯住槽溝,又能在送入多絲紗 絲紗能由篩孔進有一,多個篩孔,當翼片關閉時,多 要一個還是多個卩彳箱=。箱體開口的位置、大小、以及需 定之。 * ΰ要依據纏繞後紗包橫向移動的長度決 能用在這裡的練 來控制纏繞後紗勹衣置敢好是有一個橫向移動裝備, 何特定的橫向移^^疋的造形。但本發明並不限於使用任 裝備,只要鲈=力裝備’相反的,趣要是習知的橫向移動 依據本發,者都可以用。 限制。例如,所Μ關於向移動裝備的位置並沒設有任何 正上方,這時f置在箱體外,最好是在多絲紗送入口的 多個篩孔的翼片Ϊ體開⑽好是_型式的,並由有一或 溝的長度要依權ΐ住它。槽溝最好是延伸與管子平行。槽 不渦廿1、向移動裝備的長度作適當的選擇。 方向丨頁向移動裝備最好是裝在箱體內,依紗移動的 體η ’遠要裝在多絲紗纏繞管的前面。這樣子即可將箱 豆开口的大小減到最小,箱體內的溫度差異得以抑止。此 外開口最好是槽構型的,還有一或多個篩孔的翼片蓋住。 槽溝最好是延伸與管子平行。 要由纏繞裝置移除纏繞後的紗包,依據本發明,還要 有適當的方法開啓這個裝置,這時,最有利的是箱體採用 可關閉的開口,俾能在旋轉抽絲及纏繞時關閉箱體,以確 保箱體內的溫度的固定。此可關閉的開口最好是一扇門, 此門能於送入絲紗或移除纏繞後紗包時打開,還能在旋轉 1237670 _ 抽絲及纏繞時關閉。這個可關閉的開口最好是安裝在箱體 的前面。短暫的開啓了門,在纏繞位置上自動更換導心桿 時就能移下纏繞後的紗包不會算是一件重要的事。 圖1是此一裝置的特別合適的圖說。纏繞裝置2含箱 體4。箱體4有下牆6、上牆8,二邊牆10、12,前牆13 及後牆16。上牆8面對多絲紗進來的方向。前牆14有門 的功能,就是,箱體4能由前牆14開啓或關閉。在後牆 16,在箱體4外安裝有驅動單元18。 上牆8有一開口 20,其形狀是槽溝,由前牆14朝後 牆16的方向延伸,與邊牆10、12平行。開口 20是部分 的被翼片22蓋住。多絲紗26能穿過篩孔24,及開口 20 而進入箱體4。因爲開口 20是由右方延伸到前牆14,當 前牆14及翼片22開啓時多絲紗26就可由箱體4的邊進 入。 由多絲紗移動方向來看,其移動方向是用圖式1的箭 頭A來表示,有一橫向移動單元28就安裝在箱體4內的 開口 20後方。橫向移動單元28是連結到及被後牆16的 驅動單元18所驅動。由多絲紗26的移動方向A來看,4 支管30被夾到安裝在箱體4的移動單元28後方旋轉紡錘 的夾頭上,紡錘又與驅動單元18連接,因此紡錘及管30 都被夾到紡錘上,得能在驅動單元18轉動時,沿著它們 的軸旋轉。 兩個溫度感知器32就安裝在箱體4內,供量測箱體4 內的溫度及控制熱流向之用。其中一個感知器32,是裝設 32 1237670 —— 發明說明續頁 在管30的後方,另一個就裝在管30的前方,此係由多絲 紗26的移動方向A來看的。 箱體4有一出口 34,它就在上牆8,還有一安裝在後 牆16的入口 36。換句話說,由多絲紗26的移動方向A 來看,出口 34是在管30之前,進口 36是在管30之後。 出口 34可以選擇性的經過循環系統40連接到加熱及吹風 單元38,此係以虛線表示在圖1,這樣子加熱的氣體可以 循環使用來減少加工成本。入口 36是經過循環系統42連 接到加熱及吹風單元36。加熱及吹風單元38加熱氣體, 如空氣,然後將氣體沿著圖1的箭頭B所示方向吹,如此 氣體就經過箱體4循環起來。裝管區域內的溫度也可由調 整經感知器32所設定加熱及吹風單元38的參數控制之。 現在說明上述裝置2的操作方法。首先,多絲紗26 必須固定,最好用氣壓槍,將其夾在夾頭30的管上。爲 這個原因,前牆14及翼片22都要打開,多絲紗26才能 進入槽溝形狀的開口 20。在多絲紗26能進入之後,繞線 機控制系統的結合操作就開始。於是前牆14及翼片22再 一次的關閉,每一多絲紗就通過其在翼片上的篩孔24。紗 跑到管30內經橫向移動而成紗包44。在纏繞多絲紗26時 ,熱的氣體就由入口 36進入箱體4內來加熱箱體及在管 30上的紗包44。熱氣此後經過出口 34到加熱及吹風單元 38到一預設的溫度範圍給纏繞後的紗包44及多絲紗26。 本發明的製法能生產在管30上乳酪般的纏繞紗包44 ,如圖2所示。纏繞紗包44在儲存時會收縮及變形或壓 33 1237670The mouth enters the box and then exits through an outlet. The best thing is that the inlet and outlet are connected so that the radon gas can circulate in a circulation system. The gas, viewed from the direction of yarn movement, must first enter the back of the tube and then be discharged from the front of the tube. Although the gas can also be heated inside the cabinet, it is best to heat it outside the cabinet to maintain a uniform temperature distribution inside the cabinet. According to the present invention, the temperature measurement in the cabinet is preferably performed by more than one temperature sensor. For consistency of the temperature of the gas, it is best to moderately heat the outside of the box, and the temperature inside the box should be set at > 45 ° C to 65 ° C. Temperature sensing: The gas heating elements are best connected to each other so that the temperature of the gas can be controlled within a preset range, preferably between > 45 ° C and 65 ° C. When measuring the temperature in the cabinet, compare it with the preset temperature, and then heat or lower or maintain the temperature of the heated gas according to the temperature difference.俾 Keep the temperature in the cabinet within the required range. The temperature inside the cabinet should be tested at at least two points. Depending on the direction of yarn movement, it is best to check that the temperature inside the box is always the same before and after the sleeve. Also adjust the gas temperature and its flow rate appropriately to prevent temperature changes. In order to feed the multi-filament yarn before the start of winding, the box preferably has an opening. Especially slot-shaped openings. The configuration of the grooves depends on the direction of the yarn movement. It is best for the multifilament yarn to enter the box horizontally. When winding, the grooves should be partially covered with appropriate methods to insulate the inside and outside of the box to avoid a temperature difference in the phase body. The method that is particularly preferred in the present invention is, the factory's: The way of covering is to use the fins to fix it on the outer surface of the box, when Xuan Guang 8.3.1 30 Invention_Month Continued On. This blade shovel is used to hold the groove like a knife, and it can feed multi-filament yarn into the sieve. There can be one or more sieve holes. When the fin is closed, one or more shovel boxes are required. =. The position, size, and opening of the cabinet opening are required. * ΰ It depends on the length of the horizontal movement of the yarn package after winding. You can use the exercises here to control the setting of the yarn package after winding. There is a horizontal movement equipment, and a specific shape of the horizontal movement ^^^. However, the present invention is not limited to the use of any equipment, as long as the perch = force equipment 'is the opposite, if the conventional horizontal movement is interesting, anyone can use it. limit. For example, the position of the moving equipment is not set directly above. At this time, f is placed outside the box, and it is better to open the flaps of the multiple screen holes of the multi-filament yarn inlet. And by the length of one or ditch to hold it in accordance with the right. The grooves preferably extend parallel to the tube. The groove is not vortex. 1. Make an appropriate choice for the length of the moving equipment. Direction 丨 The page-moving equipment is preferably installed in the box, and the body η ′ that is moved by the yarn is far from the front of the multi-filament yarn winding tube. In this way, the size of the opening of the box bean can be minimized, and the temperature difference in the box can be suppressed. The external openings are preferably slot-shaped and covered by one or more screen fins. The grooves preferably extend parallel to the tube. To remove the wrapped yarn package by the winding device, according to the present invention, there must be an appropriate method to open the device. At this time, it is most advantageous that the box adopts a closable opening, which can be closed when spinning and spinning. Cabinet to ensure that the temperature inside the cabinet is fixed. The closable opening is preferably a door that can be opened when feeding silk yarn or removing the wrapped bag after winding, and can be closed when spinning 1237670 _ drawing and winding. This closable opening is best installed in the front of the cabinet. The door is opened briefly, and it is not important to be able to remove the wrapped yarn package when the guide rod is automatically changed in the winding position. Figure 1 is a particularly suitable illustration of such a device. The winding device 2 contains a case 4. The cabinet 4 has a lower wall 6, an upper wall 8, two side walls 10 and 12, a front wall 13 and a rear wall 16. The upper wall 8 faces the direction in which the multifilament yarn comes in. The front wall 14 has the function of a door, that is, the cabinet 4 can be opened or closed by the front wall 14. A drive unit 18 is mounted on the rear wall 16 outside the case 4. The upper wall 8 has an opening 20 in the shape of a groove, extending from the front wall 14 toward the rear wall 16 and parallel to the side walls 10,12. The opening 20 is partially covered by the flap 22. The multifilament yarn 26 can pass through the sieve opening 24 and the opening 20 to enter the case 4. Because the opening 20 extends from the right side to the front wall 14, the multi-filament yarn 26 can enter from the side of the box 4 when the front wall 14 and the flap 22 are opened. Judging from the moving direction of the multifilament yarn, its moving direction is indicated by the arrow A in Fig. 1. A lateral moving unit 28 is installed behind the opening 20 in the box 4. The lateral moving unit 28 is connected to and driven by a driving unit 18 of the back wall 16. Viewed from the moving direction A of the multifilament yarn 26, the four tubes 30 are clamped to the chuck of the rotating spindle installed behind the moving unit 28 of the casing 4, and the spindle is connected to the driving unit 18, so the spindle and the tube 30 are clamped On the spindles, it is necessary to be able to rotate along their axis as the drive unit 18 rotates. Two temperature sensors 32 are installed in the box 4 for measuring the temperature in the box 4 and controlling the direction of heat flow. One of the sensors 32 is installed 32 1237670-Description of the invention continued on the back of the tube 30, and the other is installed in front of the tube 30, which is viewed from the moving direction A of the multifilament yarn 26. The cabinet 4 has an outlet 34, which is located on the upper wall 8, and an inlet 36 which is installed on the rear wall 16. In other words, viewed from the moving direction A of the multifilament yarn 26, the outlet 34 is before the tube 30, and the inlet 36 is after the tube 30. The outlet 34 can be optionally connected to the heating and blowing unit 38 through the circulation system 40, which is shown in dotted lines in FIG. 1, so that the heated gas can be recycled to reduce processing costs. The inlet 36 is connected to the heating and blowing unit 36 via a circulation system 42. The heating and blowing unit 38 heats the gas, such as air, and then blows the gas in the direction shown by the arrow B in FIG. 1, so that the gas circulates through the box 4. The temperature in the tube filling area can also be controlled by adjusting the parameters of the heating and blowing unit 38 set by the sensor 32. The operation method of the above-mentioned device 2 will now be described. First of all, the multifilament yarn 26 must be fixed, and it is preferably clamped on the tube of the collet 30 using a pneumatic gun. For this reason, the front wall 14 and the flaps 22 must be opened so that the multifilament yarn 26 can enter the slot-shaped opening 20. After the multifilament yarn 26 can be entered, the combined operation of the winding machine control system is started. The front wall 14 and the flaps 22 are closed again, and each multifilament yarn passes through its screen holes 24 on the flaps. The yarn runs into the tube 30 and moves laterally to form a yarn package 44. When the multifilament yarn 26 is wound, the hot gas enters the case 4 through the inlet 36 to heat the case and the yarn package 44 on the tube 30. The hot air then passes through the outlet 34 to the heating and blowing unit 38 to a preset temperature range to the wrapped yarn package 44 and the multifilament yarn 26. The method of the present invention can produce a cheese-like winding gauze 44 on the tube 30, as shown in FIG. Winding gauze 44 shrinks and deforms or compresses during storage 33 1237670
熔化,用齒輪定量幫浦進料到進料器,在這裏順著流向由 噴嘴進入聚酯成分中。這兩個熔漿於是均勻混合最後分散 到Sulzer的SMX靜態混合器,此混合器有15個元件,內 直徑爲15mm。It melts and is fed into the feeder with a fixed-quantity pump by a gear, where it flows into the polyester component through the nozzle. The two melts were then mixed uniformly and finally dispersed into Sulzer's SMX static mixer, which had 15 elements and an inner diameter of 15mm.
Plexiglas7N 的熔漿黏度是 810Pas (在 2·4Ηζ 及 255°C ),結果是其添加劑與聚酯熔漿黏度的比例是2.5 : 1 ° 熔漿的輸送量是63g/min,滞留時間6min ’由旋轉抽 絲成型幫浦到紡織突起機的流量調節在POY線性密度約 102dtex。要用各種不同的捲動速度設定。在旋轉抽絲成型 幫浦下方與進入紡織突起機入口的上面,安裝一具Fluitec 的HD-CSE.型靜態混合器,此器有1個元件,其內直徑爲 10mm。產品線的二次加熱系統及旋轉抽絲成型裝置,包 括幫浦及紡織突起機,均設定在255°C。紡織突起機內有 30mni局’ 350- 500 "m的鋼砂、20 βπι非針織以及40 "rn 針織物的過濾器作爲過濾媒介。熔漿是經過80mm直徑紡 織突起板而壓擠出來,此板有34個孔,直徑0.25mm及長 1.0mm。鑄模壓力大槪是120— l4〇bai·。 冷卻延遲區100mm長,有30mm加熱牆及70mm絕 緣及沒有加熱的框架。熔融的細絲最後由空氣水平的吹著 旋轉抽絲成型線,長1500mm。冷卻空氣的流量是0.35m/sec ,溫度18°C,相對濕度80%。細絲至紡織突起機下方800 mm處成爲固體。 在距離紡織突起機約l〇50mm處有加油機,在聚集前 ,先將整理油加在成型的絲上直到終點。加油機有Tribofil 38 1237670Plexiglas7N has a melt viscosity of 810Pas (at 2 · 4Ηζ and 255 ° C). As a result, the ratio of its additive to the viscosity of the polyester melt is 2.5: 1 ° The throughput of the melt is 63g / min, and the residence time is 6min. The flow rate of the spinning spinning pump to the textile protrusion machine is adjusted at a POY linear density of about 102 dtex. Use various scroll speed settings. A Fluitec HD-CSE. Type static mixer is installed below the rotary wire-drawing pump and above the entrance of the textile protrusion machine. This device has one element with an inner diameter of 10mm. The product line's secondary heating system and rotary wire drawing molding device, including pumps and textile protrusion machines, are set at 255 ° C. Inside the weaving machine, there are 30mni round ’350-500 " m steel grit, 20 βπ non-knitted and 40 " rn knitted fabric filters as filter media. The melt is extruded through a 80mm diameter woven protruding plate. The plate has 34 holes, a diameter of 0.25mm and a length of 1.0mm. The pressure of the mold is 120-1400. The cooling delay zone is 100mm long, with 30mm heated walls, 70mm insulation and unheated frames. The molten filaments were finally blown by air to rotate the wire drawing forming line, and the length was 1500 mm. The cooling air flow is 0.35m / sec, the temperature is 18 ° C, and the relative humidity is 80%. The filament becomes solid at 800 mm below the textile protrusion machine. There is a dispenser at about 1050mm away from the textile protrusion machine. Before the gathering, the finishing oil is first added to the formed yarn to the end point. Tanker with Tribofil 38 1237670
表面及入口直徑lmm。使用的劑量是〇·4〇%,依據纖維重 量而定。 聚集的旋轉抽絲成型線然後送到纏繞機。加油機與第 一取出滾筒間的距離是3.2m。調節時間在95及140ms間 。一對滾筒,被紗繞成S形。在滾筒間是TEMCO捲入噴 嘴’操作時採用的空氣壓力是1.5bar。爲與速度設定一致 ’ BARMAG SW6繞線機的捲動速度的設定要與取出紗的 張力6cN相當。繞線機係裝在一盒子內,空氣經過加熱並 由鼓風機送入此盒內。此盒有一環扣,控制溫度在63°C 土 1_5°C之間,它在盒子內的位置是離旋轉紗包20cm。使用 添加劑的聚酯絲紗,不論用量多少,其生產力都有顯著增 加,十公斤的捲線軸可以立刻自繞線機上取下,所完成的 POY紗,縱在DIN 53802標準條件下儲存四週,仍可保持 其原有的材質。在纏繞後立即量測的沸騰收縮是5到8% ,比儲存後的捲線軸高不到2%。織紋與染色均性極佳。 就POY速度而言,其使用的最大拉伸比例已是令人驚訝的 高。依據EPS 0080274第6頁第51行的定義,拉伸比例 =(1 + POY伸長(%)/1〇〇)。爲了模擬,有這些參數的捲 線軸在加熱箱暴露在60°0溫度爲時20小時’結果捲線軸 形狀及織物資料的改變都不顯著。 比較實施例4 重複發明實施例1 ’所不同的是:添加物定量系統沒 有與產品線連線,所以沒有添加伸長加強劑。此外移除了 繞線機盒,又在同一量測點上設定34°c的溫度。其時纏繞 39 1237670Surface and entrance diameter lmm. The dose used is 0.4%, depending on the fiber weight. The gathered spinning wire is then sent to a winding machine. The distance between the dispenser and the first take-out drum is 3.2m. The adjustment time is between 95 and 140ms. A pair of rollers, the yarn is wound into an S shape. The TEMCO roll-in nozzle is used between the drums to operate the air pressure of 1.5 bar. To be consistent with the speed setting ’The setting of the winding speed of the BARMAG SW6 winder should be equivalent to the tension 6cN of the yarn taken out. The winding machine is installed in a box, and the air is heated and sent into the box by a blower. This box has a ring buckle, the temperature is controlled between 63 ° C and 1-5 ° C, and its position in the box is 20cm from the spinning gauze. The polyester yarn using additives has a significant increase in productivity regardless of the amount used. The ten-kilogram reel can be immediately removed from the winding machine. The completed POY yarn is stored for four weeks under DIN 53802 standards It still retains its original texture. The boiling shrinkage measured immediately after winding is 5 to 8%, which is less than 2% higher than the reel after storage. Excellent weave and dyeing uniformity. As far as POY speed is concerned, the maximum draw ratio used is already surprisingly high. According to the definition of EPS 0080274, page 6, line 51, the stretching ratio = (1 + POY elongation (%) / 100). For simulation, the spools with these parameters were exposed to a temperature of 60 ° 0 in the heating box for 20 hours. As a result, the shape of the spool and the fabric information were not significantly changed. Comparative Example 4 The same thing as Example 1 of the invention was repeated. The difference was that the additive dosing system was not connected to the product line, so no elongation enhancer was added. In addition, the winding box was removed and a temperature of 34 ° c was set at the same measurement point. Entangling 39 1237670
紗包的室溫是24°C。 與發明範例1比較,因缺少伸長加強劑以致其伸長率 較低。從而最大DR其最大拉伸比例也較低。所以它的旋 轉抽絲成型的能量及經濟效益皆低。又因纏繞紗包的熱處 理不適當導致沸騰收縮祗有53%,此與儲存後的44%只 少了 9%絕對値。此後6(TC的熱處理也會減少其沸騰收縮 約44% (絕對値)。 其他參數與特性資料詳表1到4。 表1實驗參數 實 驗 參 數 發明實施例1 發明實施例2 添加劑濃度 (%) 0.7 1.0 取出速度 (m/min ) 3520 4022 捲動速度 (m/min ) 3500 4000 紡織突起機伸長率 182 181 紗張力 滾筒上方1 (cN) 15.5 16 滾筒1間最大 (cN) 13 12.5 滾筒上方2 (cN/dtex ) 0.15 0.16 滾筒2間最大 (cN/dtex ) 0.13 0.12 纏繞紗張力1 (cN) 5.9 6.4 纏繞紗張力2 (cN/dtex ) 0.058 0.062 繞線機盒 是 是 1 :絕對 2 2:根據線性密度測定The room temperature of the gauze is 24 ° C. Compared with Invention Example 1, the elongation is low due to the lack of an elongation reinforcing agent. Therefore, the maximum DR has a lower maximum stretching ratio. Therefore, the energy and economic benefits of its spinning and drawing are low. In addition, due to improper heat treatment of the wrapped yarn package, the boiling shrinkage was 53%, which was only 9% less than the 44% after storage. After 6 (heat treatment of TC will also reduce its boiling shrinkage by about 44% (absolute 値). Other parameters and characteristics are detailed in Tables 1 to 4. Table 1 Experimental parameters Experimental parameters Invention Example 1 Invention Example 2 Additive concentration (%) 0.7 1.0 Take-off speed (m / min) 3520 4022 Rolling speed (m / min) 3500 4000 Textile protrusion machine elongation 182 181 Yarn tension above the roller 1 (cN) 15.5 16 Max. Between rollers 1 (cN) 13 12.5 Above the roller 2 (cN / dtex) 0.15 0.16 Max. (cN / dtex) 0.13 0.12 Winding yarn tension 1 (cN) 5.9 6.4 Winding yarn tension 2 (cN / dtex) 0.058 0.062 The winding box is 1: absolute 2 2: Based on linear density determination
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10213921A DE10213921B4 (en) | 2002-03-28 | 2002-03-28 | A method of spinning and winding polyester multifilament yarns using spin additives and polyester multifilament yarns obtainable by the spinning process |
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| TW200404108A TW200404108A (en) | 2004-03-16 |
| TWI237670B true TWI237670B (en) | 2005-08-11 |
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| TW092104464A TWI237670B (en) | 2002-03-28 | 2003-03-03 | Spinning and winding of polyester multifilament yarns using spinning additives and polyester multifilament yarns obtainable by the spinning process |
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| US (1) | US20050269439A1 (en) |
| CN (1) | CN1306083C (en) |
| AU (1) | AU2003215578A1 (en) |
| DE (1) | DE10213921B4 (en) |
| TR (1) | TR200402472T2 (en) |
| TW (1) | TWI237670B (en) |
| WO (1) | WO2003083190A1 (en) |
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| DE10315873A1 (en) * | 2003-04-08 | 2004-10-21 | Saurer Gmbh & Co. Kg | Device for spinning and winding synthetic threads |
| TW200741049A (en) * | 2005-12-27 | 2007-11-01 | Shell Int Research | Polyester yarn and process for producing |
| JP5992442B2 (en) * | 2011-01-13 | 2016-09-14 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | Formation and drying of copolymer fibers |
| CN109052048A (en) * | 2018-09-05 | 2018-12-21 | 佛山市三创针织有限公司 | It is a kind of to smear uniform textile machinery yarn waxing device |
| EP3835480B1 (en) * | 2019-12-10 | 2025-03-19 | Aladdin Manufacturing Corporation | Combination yarn |
| CN114753014B (en) * | 2022-04-19 | 2023-08-15 | 泗县微腾知识产权运营有限公司 | Chemical fiber spinning equipment for textile fabric production |
| CN114808169B (en) * | 2022-04-28 | 2023-03-31 | 江苏国望高科纤维有限公司 | Sand leveling device |
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| US667096A (en) * | 1900-08-07 | 1901-01-29 | Marie Gregg Lippincott | Siphon-filler. |
| US4893483A (en) * | 1987-09-18 | 1990-01-16 | Nikku Industry Co., Ltd. | Heat treatment apparatus for bobbins of yarn |
| EP0731196B1 (en) * | 1995-02-23 | 1999-05-06 | B a r m a g AG | Method for the spinning, drawing and winding up of a synthetic yarn |
| DE19650226A1 (en) * | 1995-12-05 | 1997-06-12 | Barmag Barmer Maschf | Spin drawing high shrinkage synthetic yarn using very hot heating surfaces |
| PT1002146E (en) * | 1997-08-05 | 2002-11-29 | Zimmer Ag | PROCESS FOR THE PROCESSING OF POLYMERIC MIXTURES TO OBTAIN FILAMENTS |
| DE19733799A1 (en) * | 1997-08-05 | 1999-02-11 | Zimmer Ag | Copolymer additive used to improve melt spinning properties of polyethylene terephthalate |
| JPH11172526A (en) * | 1997-11-26 | 1999-06-29 | Asahi Chem Ind Co Ltd | Polyester fiber having low thermal stress and spinning thereof |
| TW522179B (en) * | 1999-07-12 | 2003-03-01 | Asahi Chemical Ind | Polyester yarn and producing method thereof |
| JP4517481B2 (en) * | 2000-09-07 | 2010-08-04 | 東レ株式会社 | Polyester undrawn yarn excellent in handleability and method for producing the same |
| US6740270B2 (en) * | 2000-10-10 | 2004-05-25 | Shell Oil Company | Spin draw process of making partially oriented yarns from polytrimethylene terephthalate |
| US20020130437A1 (en) * | 2000-11-03 | 2002-09-19 | Dietmar Wandel | Method of spinning, spooling, and stretch texturing Polyester filaments and polyesters thereby produced |
| US20020132116A1 (en) * | 2000-11-03 | 2002-09-19 | Dietmar Wandel | Method of spinning, spooling, and stretch texturing polyester filaments and polyesters thereby produced |
| DE10151875A1 (en) * | 2000-11-03 | 2002-08-29 | Zimmer Ag | Production of melt spun and preoriented polyester filaments with a structured polyester composition involves set cooling and drawing gaps for winding to give relatively long bobbin storage times without shrinkage |
| US20030004301A1 (en) * | 2000-11-03 | 2003-01-02 | Dietmar Wandel | Method of spinning, spooling, and stretch texturing polyester filaments and polyester filaments thereby produced |
| CN1316080C (en) * | 2002-02-12 | 2007-05-16 | 齐默尔股份公司 | A process for the production and for the winding of polyester multi-filament yarns as well as the polyester multi-filament yarns obtainable by said method and a device for the winding of one or more m |
| US6921803B2 (en) * | 2002-07-11 | 2005-07-26 | E.I. Du Pont De Nemours And Company | Poly(trimethylene terephthalate) fibers, their manufacture and use |
| EP1482077A1 (en) * | 2003-05-21 | 2004-12-01 | Zimmer AG | Polyester multi-filament yarns, process for their production and winding and winding device |
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2002
- 2002-03-28 DE DE10213921A patent/DE10213921B4/en not_active Expired - Fee Related
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2003
- 2003-02-21 AU AU2003215578A patent/AU2003215578A1/en not_active Abandoned
- 2003-02-21 WO PCT/EP2003/001783 patent/WO2003083190A1/en not_active Ceased
- 2003-02-21 US US10/508,961 patent/US20050269439A1/en not_active Abandoned
- 2003-02-21 CN CNB038073137A patent/CN1306083C/en not_active Expired - Fee Related
- 2003-02-21 TR TR2004/02472T patent/TR200402472T2/en unknown
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| Publication number | Publication date |
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| TR200402472T2 (en) | 2005-08-22 |
| CN1643191A (en) | 2005-07-20 |
| WO2003083190A1 (en) | 2003-10-09 |
| TW200404108A (en) | 2004-03-16 |
| DE10213921B4 (en) | 2006-10-12 |
| CN1306083C (en) | 2007-03-21 |
| US20050269439A1 (en) | 2005-12-08 |
| AU2003215578A1 (en) | 2003-10-13 |
| DE10213921A1 (en) | 2003-10-30 |
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