US3576773A - Polyester based fibers comprising a non-linear branched ethylene terephthalate polymers - Google Patents
Polyester based fibers comprising a non-linear branched ethylene terephthalate polymers Download PDFInfo
- Publication number
- US3576773A US3576773A US829954A US3576773DA US3576773A US 3576773 A US3576773 A US 3576773A US 829954 A US829954 A US 829954A US 3576773D A US3576773D A US 3576773DA US 3576773 A US3576773 A US 3576773A
- Authority
- US
- United States
- Prior art keywords
- viscosity
- fabric
- acid
- fibers
- polyester
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000835 fiber Substances 0.000 title abstract description 36
- 229920000728 polyester Polymers 0.000 title abstract description 29
- 229920000642 polymer Polymers 0.000 title description 21
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 title description 4
- 239000005020 polyethylene terephthalate Substances 0.000 abstract description 4
- 238000002074 melt spinning Methods 0.000 abstract description 2
- 239000004744 fabric Substances 0.000 description 31
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 23
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 210000002268 wool Anatomy 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- -1 polyethylene terephthalate Polymers 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 8
- 230000001680 brushing effect Effects 0.000 description 8
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 8
- 239000006187 pill Substances 0.000 description 8
- 206010061592 cardiac fibrillation Diseases 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- 230000002600 fibrillogenic effect Effects 0.000 description 7
- 239000002759 woven fabric Substances 0.000 description 7
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 6
- 239000006085 branching agent Substances 0.000 description 6
- 229920000139 polyethylene terephthalate Polymers 0.000 description 5
- 238000005299 abrasion Methods 0.000 description 4
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 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 4
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 3
- RGCHNYAILFZUPL-UHFFFAOYSA-N trimethyl benzene-1,3,5-tricarboxylate Chemical compound COC(=O)C1=CC(C(=O)OC)=CC(C(=O)OC)=C1 RGCHNYAILFZUPL-UHFFFAOYSA-N 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- QPYKYDBKQYZEKG-UHFFFAOYSA-N 2,2-dimethylpropane-1,1-diol Chemical compound CC(C)(C)C(O)O QPYKYDBKQYZEKG-UHFFFAOYSA-N 0.000 description 2
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 2
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 2
- WGLQHUKCXBXUDV-UHFFFAOYSA-N 3-aminophthalic acid Chemical compound NC1=CC=CC(C(O)=O)=C1C(O)=O WGLQHUKCXBXUDV-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- AEBIBBWVNCPTNL-UHFFFAOYSA-N [1-(hydroxymethyl)cyclobutyl]methanol Chemical compound OCC1(CO)CCC1 AEBIBBWVNCPTNL-UHFFFAOYSA-N 0.000 description 2
- XMUZQOKACOLCSS-UHFFFAOYSA-N [2-(hydroxymethyl)phenyl]methanol Chemical compound OCC1=CC=CC=C1CO XMUZQOKACOLCSS-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
- 229910000410 antimony oxide Inorganic materials 0.000 description 2
- GGNQRNBDZQJCCN-UHFFFAOYSA-N benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 2
- 239000001639 calcium acetate Substances 0.000 description 2
- 229960005147 calcium acetate Drugs 0.000 description 2
- 235000011092 calcium acetate Nutrition 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- INSRQEMEVAMETL-UHFFFAOYSA-N decane-1,1-diol Chemical compound CCCCCCCCCC(O)O INSRQEMEVAMETL-UHFFFAOYSA-N 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 2
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-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
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 2
- 235000020778 linoleic acid Nutrition 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 229920000909 polytetrahydrofuran Polymers 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
- PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 description 1
- QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 description 1
- BXGYYDRIMBPOMN-UHFFFAOYSA-N 2-(hydroxymethoxy)ethoxymethanol Chemical compound OCOCCOCO BXGYYDRIMBPOMN-UHFFFAOYSA-N 0.000 description 1
- MBMIMBPSXVDDRT-UHFFFAOYSA-N 2-hydroxy-3-methoxycarbonylbenzoic acid Chemical compound COC(=O)C1=CC=CC(C(O)=O)=C1O MBMIMBPSXVDDRT-UHFFFAOYSA-N 0.000 description 1
- WVDGHGISNBRCAO-UHFFFAOYSA-N 2-hydroxyisophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1O WVDGHGISNBRCAO-UHFFFAOYSA-N 0.000 description 1
- KYXHKHDZJSDWEF-LHLOQNFPSA-N CCCCCCC1=C(CCCCCC)C(\C=C\CCCCCCCC(O)=O)C(CCCCCCCC(O)=O)CC1 Chemical compound CCCCCCC1=C(CCCCCC)C(\C=C\CCCCCCCC(O)=O)C(CCCCCCCC(O)=O)CC1 KYXHKHDZJSDWEF-LHLOQNFPSA-N 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 description 1
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-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
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 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
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 229940049920 malate Drugs 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 208000022823 partial androgen insensitivity syndrome Diseases 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003503 terephthalic acid derivatives Chemical class 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
Images
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
- D01F6/58—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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
-
- 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
- D01F6/78—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products
- D01F6/84—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products from copolyesters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/82—Preparation processes characterised by the catalyst used
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/92—Synthetic fiber dyeing
- Y10S8/922—Polyester fiber
Definitions
- This invention relates to polyester fibers and a process for their preparation.
- the present invention provides oriented polyethylene terephthalate fibers which are easily accessible industrially and yarns of fibers which do not give rise to pilling. Accordingly this invention provides a polyester-based fiber having an elongation at break of greater than and a tensile strength of 18 to 36 g./tex which comprises a branched polyethylene terephthalate having a specific viscosity of 0.47 to 0.72 and a melt viscosity of 600 to 2500 poises at 285 C.
- the fibers of this invention may be used in the manufacture of woven or knitted fabrics which substantially do not form pills.
- the elongation of the fibers of this invention may vary within wide limits. When they are used in admixture with wool and cotton, fibers having elongations of 25 to 60% are chosen.
- the points representing fibres of this invention are loca-ted within the area ABCD of FIG. l of the accompanying drawing.
- the segment AB corresponds to the polymers having a viscosity 600 poises and the segment DC to the polymers having a viscosity 2,500 poises.
- the fibers currently sold commercially correspond to points above the segment BC.
- the fibers of this invention may be prepared by extruding, in the fused state a branched polyethylene tercphthalate containing y/ 11;-2 to z/ n-Z equivalent percent of n-valent chain units where n is 3 or 4, y is 0.2 and z is 2 having a specific viscosity of 0.47 to 0.72 and a melt viscosity of 600 to 2500 poises and orienting the yarns thus obtained by stretching.
- the polymers used to prepare the products of this in- 'vention are branched polyethylene terephthalates and may be prepared by incorporating a branching agent, having three or four groups capable of forming stable bonds, such as ester, ether or amide bonds with the acid or alcohol groups, into the monomer mixture.
- the preferred branching agents are polyols such as trimethylolpropane, trimethylolethane, pentaerythritol or glycerine; polyacids such as trimesic acid, trimellitic acid or anhydride or pyromellitic acid or anhydride; polyphenols such as phloroglucinol or hydroxyhydroquinone; amino acids and acid-alcohols such as hydroxyisophthalic acid or aminophthalic acid; 2,2-bis(4epoxypropoxyphenyl) -propane or diethanolamine.
- polyols such as trimethylolpropane, trimethylolethane, pentaerythritol or glycerine
- polyacids such as trimesic acid, trimellitic acid or anhydride or pyromellitic acid or anhydride
- polyphenols such as phloroglucinol or hydroxyhydroquinone
- amino acids and acid-alcohols such as
- polyester synthesis employed 0.2 to 2 mols percent of the trifunctonal branching agent relative to the terephthalic acid, or the terephthalic acid derivative, ⁇ are used. Amounts of the order of 0.1 to 1 mol percent are preferred.
- the polyesters which may be used in the process of this invention are essentially derived from terephthalic acid, ethylene glycol and a branching agent. They can however contain a proportion, up to 10 mol percent, of another glycol containing an aliphatic, cycloaliphatic or aromatic group or hetero-atoms such as propanediol, butanediol, hexanediol, decanediol, dimethylpropanediol, cyclohexanedimethanol, cyclobutanedimethanol, xylylene glycol, polyoxyethylene Iglycol of molecular weight less than 6,000, polytetrahydrofuran, another diacid such as adipic, sebacic, dodecanedioic, isophthalic or hexahydroor terephthalic acid, or dimeric acids derived from linoleic acid.
- another glycol containing an aliphatic, cycloaliphatic
- These polymers are preferaably prepared in the presence of the usual transesterification and polycondensation catalysts and may contain agents to improve their colour or heat stability such as phosphorus derivatives e.g. phosphorous acid, phosphoric acid, phenylphosphonic acid or triphenylphosphite. They can also be matted, for example by adding a suspension of titanium oxide.
- agents to improve their colour or heat stability such as phosphorus derivatives e.g. phosphorous acid, phosphoric acid, phenylphosphonic acid or triphenylphosphite.
- They can also be matted, for example by adding a suspension of titanium oxide.
- Melt viscosity the viscosity in poises of the fused mass measured at 285 C.
- Pilling the pilling observed after 30 minutes of the so-called Random Tumble Pilling Test or RTPT (Standard Specification ASTM D 1,375-64), the index l 4 so as to form a yarn of 40/1 count and with a right-hand twist of 630 (coefficient of twist 100), and this yarn is then woven into a twill fabric.
- the woven fabric is desized, heat-set, dyed in the presence of a carrier, singed, brushed and cropped in accordance with the usual processes.
- This Ethylene glycol 361 tendency to form pills for practical purposes can not Calcium acetate 0.805 be improved because the use of polymer or lower mo- Antimony oxide 0.110 lecular weight gives melt viscosities of less than 600 Trimethyl trimesate 1 9.5 poises, incompatible with good industrial spinning.
- This polymer is spun at 278 C. through a spinneret on ffhe ciber hand Standard Polyester ihefs 0f SPewith 168 0.50 mm. diameter holes and the yarn is wound miic Viscosity 0-57: stretched t0 give al1 elongation at up at a speed of 900 meters per minute No adhesion be break of 22%, and converted to a fabric under the same tween the laments is Observed. conditions as above, show considerable bleaching at the After assembling several yarns, the cable is stretched at Points 0f maximum rubbing due to briilation- 100 meters per minute in a sizing bath heated to 70 C., EXAMPLE 3 EL; grrlvirr?
- Example l using a mixture of dimethyl terephthalate, ethylene glycol, calcium acetate and phosphorous acid as in Example l, and 0.008 part of antimony oxide, it is pos- Melt viscosity Tensile Elonga- Experiment Specific (poises at Gauge strength tion at Woven Pilling Number viscosity 285 C.) (deciter) (g./tex) break fabric RTPT Fibrillation 1 0. 57 1, 200 3. 3 25 39 TWilL 5 Nil.
- the knitted fabric When subjected to the pilling test the knitted fabric has an index of 4, which is excellent for this type of article. If the knitted fabric is subjected to brushing and cropping the index is then 5.
- a knitted fabric obtained from a yarn of 40/1 count and coeicient of twist of 85, in a polyester/ wool mixture in the proportion of 70/ 30, is rated as 3 in the same test, and as 4-5 after cropping and brushing.
- a knitted fabric prepared from the standard polyester described in Example 1 and treated under the same conditions is rated as follows:
- EXAMPLE A polymer containing 1.6 equivalents of chain links derived from trimethylolpropane is prepared, spun, and knitted as above, and tested as a 70/ 30 mixture with wool.
- EXAMPLE l 1 The polymer prepared in Example 8 is spun and stretched to give individual bers having the following properties:
- EXAMPLE 12 The fiber of Example 11 is mixed with cotton in the proportion of 50/50 and spun into 501/ 1 (count) with a 915 right-hand twist (coefficient 130), and then knitted into gauge 20 interlock.
- the knitted fabric After heat-setting at 210 C. and bluing in a bath, the knitted fabric is RTP'I tested and rated at 4, which is acceptable for this type of article.
- EXAMPLE 13 A polyester which is branched with 0.8 mol percent of trimethylolpropane and which contains 6% by weight of polyoxyethylene glycol is prepared under the conditions described in Example 1 until a viscosity in the fused A11 unbranched copolyester of the same specific viscosity has the following properties under the same conditions:
- EXAMPLE 14 This same ber :mixed with wool 70/ 30 and spun into 36/1 (count) is knitted and RTPT tested after setting and dyeing.
- the knitted fabric is rated: 3-4 After cropping and brushing, the knited fabric is rated:
- ethylene terephthalate polymer contains up to l0 mol percent of propanediol, butanediol, hexanediol, decanediol, dimethyl-propanediol, cyclohexane, dimethanol, cyclobutanedimethanol, xylylene glycol, polyoxyethylene glycol of molecular weight less than 6000, polytetrahydrofuran, adipic acid, sebacic acid, dodecanedioic acid, isophthalic acid, hexahydroisophthalic acid, terephthalic acid, a
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Artificial Filaments (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR69050064 | 1968-06-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3576773A true US3576773A (en) | 1971-04-27 |
Family
ID=9695395
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US829954A Expired - Lifetime US3576773A (en) | 1968-06-04 | 1969-06-03 | Polyester based fibers comprising a non-linear branched ethylene terephthalate polymers |
Country Status (10)
Country | Link |
---|---|
US (1) | US3576773A (enrdf_load_stackoverflow) |
AT (1) | AT303952B (enrdf_load_stackoverflow) |
BE (1) | BE734017A (enrdf_load_stackoverflow) |
BR (1) | BR6909153D0 (enrdf_load_stackoverflow) |
CH (1) | CH518380A (enrdf_load_stackoverflow) |
DE (1) | DE1928436B2 (enrdf_load_stackoverflow) |
FR (1) | FR1603030A (enrdf_load_stackoverflow) |
GB (1) | GB1270852A (enrdf_load_stackoverflow) |
LU (1) | LU58790A1 (enrdf_load_stackoverflow) |
NL (1) | NL6908117A (enrdf_load_stackoverflow) |
Cited By (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3960817A (en) * | 1970-10-23 | 1976-06-01 | Ciba-Geigy Ag | Solid phase polyester polycondensation |
US4092299A (en) * | 1976-06-23 | 1978-05-30 | Monsanto Company | High draw ratio polyester feed yarn and its draw texturing |
US4217440A (en) * | 1979-08-20 | 1980-08-12 | Eastman Kodak Company | Method for making branched polyesters reproducibly |
US4383106A (en) * | 1981-09-21 | 1983-05-10 | The Goodyear Tire & Rubber Company | High melt strength elastomeric copolyesters |
US4461298A (en) * | 1982-07-26 | 1984-07-24 | Ethicon, Inc. | Composite sutures of silk and hydrophobic thermoplastic elastomers |
US4666454A (en) * | 1985-09-09 | 1987-05-19 | Celanese Corporation | Production of a fabric containing polyethylene terephthalate fibers having a reduced tendency to pill |
EP0268868A3 (en) * | 1986-11-07 | 1990-05-09 | SPOFA Spojené Podniky Pro Zdravotnickou Vyrobu | Pharmaceutical compositions for the treatment of gastro-intestinal diseases |
US5034174A (en) * | 1986-09-12 | 1991-07-23 | E. I. Du Pont De Nemours And Company | Texturing yarns |
US5045260A (en) * | 1985-06-21 | 1991-09-03 | Rhone-Poulenc Viscosuisse Sa | Polyester yarn and method for its manufacture |
GB2245275A (en) * | 1990-04-05 | 1992-01-02 | Rhone Poulenc Fibres | Process for obtaining modified polyethylene terephthalate useful for making pi lling-free fibres |
EP0474418A3 (en) * | 1990-08-28 | 1992-07-01 | Hoechst Celanese Corporation | Polyester copolymer fiber having enhanced strength and dyeability properties |
US5180793A (en) * | 1991-12-31 | 1993-01-19 | Hoechst Celanese Corporation | Flame resistant, low pilling polyester fiber |
USH1275H (en) | 1991-09-30 | 1994-01-04 | E. I. Du Pont De Nemours And Company | Polyester fibers |
US5322921A (en) * | 1985-06-21 | 1994-06-21 | Rhone-Poulenc Viscosuisse Sa | Polyester yarn |
EP0604973A1 (en) * | 1992-12-31 | 1994-07-06 | Hoechst Celanese Corporation | Low pilling polyester blended yarn |
US5442036A (en) * | 1994-09-06 | 1995-08-15 | Eastman Chemical Company | Branched copolyesters especially suitable for extrusion blow molding |
US5817740A (en) * | 1997-02-12 | 1998-10-06 | E. I. Du Pont De Nemours And Company | Low pill polyester |
WO1999019548A1 (en) * | 1997-10-14 | 1999-04-22 | Wellman, Inc. | Modified polyester with high intrinsic viscosity at moderate strength |
US5968649A (en) * | 1995-06-30 | 1999-10-19 | E. I. Du Pont De Nemours And Company | Drawing of polyester filaments |
US6013368A (en) * | 1995-06-30 | 2000-01-11 | E. I. Du Pont De Nemours And Company | Comfort by mixing deniers |
WO2000012793A1 (en) * | 1998-08-28 | 2000-03-09 | Wellman, Inc. | Polyester modified with polyethylene glycol and pentaerythritol |
US6037055A (en) * | 1997-02-12 | 2000-03-14 | E. I. Du Pont De Nemours And Company | Low pill copolyester |
EP0985752A1 (de) * | 1998-09-10 | 2000-03-15 | Lurgi Zimmer Aktiengesellschaft | Copolyesterfaser |
WO2001036723A1 (en) * | 1999-11-19 | 2001-05-25 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
US6291066B1 (en) | 1999-11-19 | 2001-09-18 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
US20020037411A1 (en) * | 2000-07-10 | 2002-03-28 | Frankfort Hans R. | Method of producing polymeric filaments |
US6509091B2 (en) | 1999-11-19 | 2003-01-21 | Wellman, Inc. | Polyethylene glycol modified polyester fibers |
US6582817B2 (en) | 1999-11-19 | 2003-06-24 | Wellman, Inc. | Nonwoven fabrics formed from polyethylene glycol modified polyester fibers and method for making the same |
US6623853B2 (en) | 1998-08-28 | 2003-09-23 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
CN102974169A (zh) * | 2012-12-28 | 2013-03-20 | 苏州大学 | 一种过滤材料及其制备方法 |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4945151A (en) * | 1989-03-08 | 1990-07-31 | E. I. Du Pont De Nemours And Company | Continuous production of polyester filaments |
US5151494A (en) * | 1991-01-04 | 1992-09-29 | Hoechst Celanese Corporation | Flame resistant, low pilling polyester fiber |
DE19951067B4 (de) * | 1999-10-22 | 2004-04-08 | Inventa-Fischer Ag | Polyesterfasern mit verminderter Pillingneigung sowie Verfahren zu ihrer Herstellung |
-
1968
- 1968-06-04 FR FR69050064A patent/FR1603030A/fr not_active Expired
-
1969
- 1969-05-26 BR BR209153/69A patent/BR6909153D0/pt unknown
- 1969-05-28 NL NL6908117A patent/NL6908117A/xx not_active Application Discontinuation
- 1969-06-03 CH CH841969A patent/CH518380A/fr not_active IP Right Cessation
- 1969-06-03 LU LU58790D patent/LU58790A1/xx unknown
- 1969-06-03 US US829954A patent/US3576773A/en not_active Expired - Lifetime
- 1969-06-03 GB GB28125/69A patent/GB1270852A/en not_active Expired
- 1969-06-03 BE BE734017D patent/BE734017A/xx not_active IP Right Cessation
- 1969-06-04 DE DE19691928436 patent/DE1928436B2/de not_active Ceased
- 1969-06-04 AT AT05313/69A patent/AT303952B/de not_active IP Right Cessation
Cited By (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3960817A (en) * | 1970-10-23 | 1976-06-01 | Ciba-Geigy Ag | Solid phase polyester polycondensation |
US4092299A (en) * | 1976-06-23 | 1978-05-30 | Monsanto Company | High draw ratio polyester feed yarn and its draw texturing |
US4217440A (en) * | 1979-08-20 | 1980-08-12 | Eastman Kodak Company | Method for making branched polyesters reproducibly |
US4383106A (en) * | 1981-09-21 | 1983-05-10 | The Goodyear Tire & Rubber Company | High melt strength elastomeric copolyesters |
US4461298A (en) * | 1982-07-26 | 1984-07-24 | Ethicon, Inc. | Composite sutures of silk and hydrophobic thermoplastic elastomers |
US5045260A (en) * | 1985-06-21 | 1991-09-03 | Rhone-Poulenc Viscosuisse Sa | Polyester yarn and method for its manufacture |
US5322921A (en) * | 1985-06-21 | 1994-06-21 | Rhone-Poulenc Viscosuisse Sa | Polyester yarn |
US4666454A (en) * | 1985-09-09 | 1987-05-19 | Celanese Corporation | Production of a fabric containing polyethylene terephthalate fibers having a reduced tendency to pill |
US5034174A (en) * | 1986-09-12 | 1991-07-23 | E. I. Du Pont De Nemours And Company | Texturing yarns |
EP0268868A3 (en) * | 1986-11-07 | 1990-05-09 | SPOFA Spojené Podniky Pro Zdravotnickou Vyrobu | Pharmaceutical compositions for the treatment of gastro-intestinal diseases |
GB2245275A (en) * | 1990-04-05 | 1992-01-02 | Rhone Poulenc Fibres | Process for obtaining modified polyethylene terephthalate useful for making pi lling-free fibres |
GB2245275B (en) * | 1990-04-05 | 1993-09-01 | Rhone Poulenc Fibres | Process for obtaining modified polyethylene terephthalate useful for making pilling-free fibres |
EP0474418A3 (en) * | 1990-08-28 | 1992-07-01 | Hoechst Celanese Corporation | Polyester copolymer fiber having enhanced strength and dyeability properties |
USH1275H (en) | 1991-09-30 | 1994-01-04 | E. I. Du Pont De Nemours And Company | Polyester fibers |
US5180793A (en) * | 1991-12-31 | 1993-01-19 | Hoechst Celanese Corporation | Flame resistant, low pilling polyester fiber |
EP0604973A1 (en) * | 1992-12-31 | 1994-07-06 | Hoechst Celanese Corporation | Low pilling polyester blended yarn |
US5442036A (en) * | 1994-09-06 | 1995-08-15 | Eastman Chemical Company | Branched copolyesters especially suitable for extrusion blow molding |
US5523382A (en) * | 1994-09-06 | 1996-06-04 | Eastman Chemical Company | Branched copolyesters especially suitable for extrusion blow molding |
US5968649A (en) * | 1995-06-30 | 1999-10-19 | E. I. Du Pont De Nemours And Company | Drawing of polyester filaments |
US6013368A (en) * | 1995-06-30 | 2000-01-11 | E. I. Du Pont De Nemours And Company | Comfort by mixing deniers |
US6214264B1 (en) * | 1995-06-30 | 2001-04-10 | E. I. Du Pont De Nemours And Company | Drawing of polyester filaments |
US5817740A (en) * | 1997-02-12 | 1998-10-06 | E. I. Du Pont De Nemours And Company | Low pill polyester |
US6037055A (en) * | 1997-02-12 | 2000-03-14 | E. I. Du Pont De Nemours And Company | Low pill copolyester |
WO1999019548A1 (en) * | 1997-10-14 | 1999-04-22 | Wellman, Inc. | Modified polyester with high intrinsic viscosity at moderate strength |
US6110587A (en) * | 1997-10-14 | 2000-08-29 | Wellman, Inc. | Modified polyester with high intrinsic viscosity at moderate strength |
US6221488B1 (en) | 1997-10-14 | 2001-04-24 | Wellman, Inc. | Modified polyester with high intrinsic viscosity at moderate strength |
WO2000012793A1 (en) * | 1998-08-28 | 2000-03-09 | Wellman, Inc. | Polyester modified with polyethylene glycol and pentaerythritol |
US6623853B2 (en) | 1998-08-28 | 2003-09-23 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
US6485829B2 (en) | 1998-08-28 | 2002-11-26 | Wellman, Inc. | Polyester modified with polyethylene glycol and pentaerythritol |
US6294254B1 (en) | 1998-08-28 | 2001-09-25 | Wellman, Inc. | Polyester modified with polyethylene glycol and pentaerythritol |
EP0985752A1 (de) * | 1998-09-10 | 2000-03-15 | Lurgi Zimmer Aktiengesellschaft | Copolyesterfaser |
US6303739B2 (en) | 1999-11-19 | 2001-10-16 | Wellman, Inc. | Method of preparing polyethylene glycol modified polyester filaments |
US6322886B2 (en) | 1999-11-19 | 2001-11-27 | Wellman, Inc. | Polyethylene glycol modified polyester fibers, yarns, and fabrics and method for making the same |
US6399705B2 (en) | 1999-11-19 | 2002-06-04 | Wellman, Inc. | Method of preparing polyethylene glycol modified polyester filaments |
US6454982B1 (en) | 1999-11-19 | 2002-09-24 | Wellman, Inc. | Method of preparing polyethylene glycol modified polyester filaments |
US6291066B1 (en) | 1999-11-19 | 2001-09-18 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
US6509091B2 (en) | 1999-11-19 | 2003-01-21 | Wellman, Inc. | Polyethylene glycol modified polyester fibers |
US6582817B2 (en) | 1999-11-19 | 2003-06-24 | Wellman, Inc. | Nonwoven fabrics formed from polyethylene glycol modified polyester fibers and method for making the same |
WO2001036723A1 (en) * | 1999-11-19 | 2001-05-25 | Wellman, Inc. | Polyethylene glycol modified polyester fibers and method for making the same |
US20020037411A1 (en) * | 2000-07-10 | 2002-03-28 | Frankfort Hans R. | Method of producing polymeric filaments |
US20040140582A1 (en) * | 2000-07-10 | 2004-07-22 | Frankfort Hans R. E. | Method of producing polymeric filaments |
CN102974169A (zh) * | 2012-12-28 | 2013-03-20 | 苏州大学 | 一种过滤材料及其制备方法 |
CN102974169B (zh) * | 2012-12-28 | 2014-07-02 | 苏州大学 | 一种过滤材料及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
AT303952B (de) | 1972-11-15 |
FR1603030A (enrdf_load_stackoverflow) | 1971-03-15 |
NL6908117A (enrdf_load_stackoverflow) | 1969-12-08 |
GB1270852A (en) | 1972-04-19 |
DE1928436B2 (de) | 1977-08-18 |
CH518380A (fr) | 1972-01-31 |
LU58790A1 (enrdf_load_stackoverflow) | 1970-01-14 |
DE1928436A1 (de) | 1969-12-11 |
BE734017A (enrdf_load_stackoverflow) | 1969-12-03 |
BR6909153D0 (pt) | 1973-01-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3576773A (en) | Polyester based fibers comprising a non-linear branched ethylene terephthalate polymers | |
US4082731A (en) | Method for producing a high modulus polyester yarn | |
US3616183A (en) | Polyester sheath-core conjugate filaments | |
US5262460A (en) | Aromatic polyester resin composition and fiber | |
US20040195543A1 (en) | Polyester based fiber and artificial hair using the same | |
US3104450A (en) | Textile material | |
US3390108A (en) | Ethylene glycol-terephthalic aciddimer acid copolyester resin | |
US3874155A (en) | Flame-retardant fiber blend | |
US3542737A (en) | Polymeric polyesters containing alkylor alkenylsuccinic acids | |
US11913168B2 (en) | Process for producing dyed mixed fibres, dyed mixed fibre yarns and/or dyed mixed fibre textile fabrics | |
US3873504A (en) | Flame-retardant copolyester resin containing dialkyl tetrabromo diphenoxyalkane dicarboxylates | |
US5331032A (en) | Hydrophilic aromatic polyester fiber | |
US4067850A (en) | Filaments and fibers having improved dyeability prepared from bis ethoxylated tetramethyl bisphenol A | |
US4026973A (en) | Process for preparing heat-resistant aromatic polyester filaments | |
US3874157A (en) | Flame-retardant fiber blend | |
US3385831A (en) | Textile fibers of polyethylene terephthalate/hexahydroterephthalate copolyester | |
AU614248B2 (en) | Solution spinning process | |
US4359557A (en) | Process for producing low pilling textile fiber and product of the process | |
US20070055043A1 (en) | Modified polyethylene, terephthalate for low temperature dyeability, controlled shrinkage characteristics and improved tensile properties | |
JP3547842B2 (ja) | 抗ピリング性異形断面繊維の製造方法 | |
US3670489A (en) | Textile yarn | |
US4071502A (en) | Polyester fiber having anti-pilling property and its production | |
KR100306316B1 (ko) | 탄성섬유,그의제조방법및그에사용된폴리에스테르엘라스토머 | |
JPH0770856A (ja) | ポリエステル被覆弾性糸 | |
US3391123A (en) | Process for melt spinning fibers |