JPH0541745B2 - - Google Patents
Info
- Publication number
- JPH0541745B2 JPH0541745B2 JP60132725A JP13272585A JPH0541745B2 JP H0541745 B2 JPH0541745 B2 JP H0541745B2 JP 60132725 A JP60132725 A JP 60132725A JP 13272585 A JP13272585 A JP 13272585A JP H0541745 B2 JPH0541745 B2 JP H0541745B2
- Authority
- JP
- Japan
- Prior art keywords
- acid
- mol
- glycol
- component
- ester
- 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
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 42
- 229920000728 polyester Polymers 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 19
- 239000003795 chemical substances by application Substances 0.000 claims description 17
- 239000002253 acid Substances 0.000 claims description 15
- 239000002202 Polyethylene glycol Substances 0.000 claims description 12
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 12
- 229920001223 polyethylene glycol Polymers 0.000 claims description 12
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 10
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 8
- 125000001931 aliphatic group Chemical group 0.000 claims description 8
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 8
- KKEYFWRCBNTPAC-UHFFFAOYSA-N terephthalic acid group Chemical group C(C1=CC=C(C(=O)O)C=C1)(=O)O KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 8
- 239000000835 fiber Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 claims description 6
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims 1
- 238000000034 method Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000004744 fabric Substances 0.000 description 6
- -1 alkylene glycol Chemical compound 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 125000002723 alicyclic group Chemical group 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000295 fuel oil Substances 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229960004275 glycolic acid Drugs 0.000 description 2
- 238000003672 processing method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- YJGUVTBNQCVSQB-UHFFFAOYSA-N 2,2-diphenylpropanedioic acid Chemical compound C=1C=CC=CC=1C(C(O)=O)(C(=O)O)C1=CC=CC=C1 YJGUVTBNQCVSQB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- ROVLJQDICPLANK-UHFFFAOYSA-N 2-ethoxy-3-hydroxybenzoic acid Chemical compound CCOC1=C(O)C=CC=C1C(O)=O ROVLJQDICPLANK-UHFFFAOYSA-N 0.000 description 1
- BTBJCTWMARHHQD-UHFFFAOYSA-N 2-heptadecylpropanedioic acid Chemical compound CCCCCCCCCCCCCCCCCC(C(O)=O)C(O)=O BTBJCTWMARHHQD-UHFFFAOYSA-N 0.000 description 1
- MTZVTGFUNNLFPX-UHFFFAOYSA-N 2-hydroxycyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC1(C(=O)O)C(C(=O)O)CCC=C1 MTZVTGFUNNLFPX-UHFFFAOYSA-N 0.000 description 1
- WMRCTEPOPAZMMN-UHFFFAOYSA-N 2-undecylpropanedioic acid Chemical compound CCCCCCCCCCCC(C(O)=O)C(O)=O WMRCTEPOPAZMMN-UHFFFAOYSA-N 0.000 description 1
- HRMCXDSWURAYFR-UHFFFAOYSA-N 3-phenoxyphthalic acid Chemical compound OC(=O)C1=CC=CC(OC=2C=CC=CC=2)=C1C(O)=O HRMCXDSWURAYFR-UHFFFAOYSA-N 0.000 description 1
- VSAWBBYYMBQKIK-UHFFFAOYSA-N 4-[[3,5-bis[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-2,4,6-trimethylphenyl]methyl]-2,6-ditert-butylphenol Chemical compound CC1=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C(CC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)C(C)=C1CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 VSAWBBYYMBQKIK-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- VBJCDSVGBUHMHU-UHFFFAOYSA-N 7-ethenyltetradecanedioic acid Chemical compound OC(=O)CCCCCCC(C=C)CCCCCC(O)=O VBJCDSVGBUHMHU-UHFFFAOYSA-N 0.000 description 1
- VNXKEQYMBSFLJJ-UHFFFAOYSA-N 8,13-dimethylicosa-8,12-dienedioic acid Chemical compound OC(=O)CCCCCCC(C)=CCCC=C(C)CCCCCCC(O)=O VNXKEQYMBSFLJJ-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- ZOIORXHNWRGPMV-UHFFFAOYSA-N acetic acid;zinc Chemical compound [Zn].CC(O)=O.CC(O)=O ZOIORXHNWRGPMV-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- MQPUYGQSVQXVTN-UHFFFAOYSA-N icosa-8,12-dienedioic acid Chemical compound OC(=O)CCCCCCC=CCCC=CCCCCCCC(O)=O MQPUYGQSVQXVTN-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
Landscapes
- Polyesters Or Polycarbonates (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13272585A JPS61291622A (ja) | 1985-06-18 | 1985-06-18 | ポリエステル系繊維加工剤 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13272585A JPS61291622A (ja) | 1985-06-18 | 1985-06-18 | ポリエステル系繊維加工剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61291622A JPS61291622A (ja) | 1986-12-22 |
| JPH0541745B2 true JPH0541745B2 (fr) | 1993-06-24 |
Family
ID=15088123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13272585A Granted JPS61291622A (ja) | 1985-06-18 | 1985-06-18 | ポリエステル系繊維加工剤 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61291622A (fr) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110467722A (zh) * | 2019-09-12 | 2019-11-19 | 武汉纺织大学 | 一种亲水聚酯及其制备方法 |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002235285A (ja) * | 2001-02-02 | 2002-08-23 | Toyobo Co Ltd | 耐久親水化された長繊維不織布 |
| DE102004029310A1 (de) * | 2004-06-17 | 2005-12-29 | Clariant Gmbh | Hochkonzentrierte, wässrige Formulierungen von Oligo-und Polyestern |
| JP4529048B2 (ja) * | 2005-04-23 | 2010-08-25 | 東洋化学株式会社 | ポリエステル系処理剤及び該処理剤で処理された被処理品 |
| JP5266602B2 (ja) * | 2005-11-21 | 2013-08-21 | 東洋製罐グループホールディングス株式会社 | 酸素吸収性樹脂、酸素吸収性樹脂組成物及び酸素吸収性容器 |
| JP5505852B2 (ja) * | 2006-07-11 | 2014-05-28 | 東洋製罐株式会社 | 酸素吸収性樹脂、酸素吸収性樹脂組成物及び酸素吸収性容器 |
| CN103321054B (zh) * | 2013-06-07 | 2016-01-13 | 张家港市德宝化工有限公司 | 一种聚酯纤维用蓬松柔软整理剂及其制备方法 |
| JP2015017341A (ja) * | 2013-07-12 | 2015-01-29 | 東洋紡Ｓｔｃ株式会社 | 伸縮性布帛およびその製造方法 |
| JP6284605B2 (ja) * | 2016-11-01 | 2018-02-28 | 東洋紡Ｓｔｃ株式会社 | 伸縮性布帛およびその製造方法 |
| JP6360589B2 (ja) * | 2017-04-27 | 2018-07-18 | 東洋紡Ｓｔｃ株式会社 | 伸縮性布帛の製造方法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5031198A (fr) * | 1973-07-24 | 1975-03-27 |
-
1985
- 1985-06-18 JP JP13272585A patent/JPS61291622A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5031198A (fr) * | 1973-07-24 | 1975-03-27 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110467722A (zh) * | 2019-09-12 | 2019-11-19 | 武汉纺织大学 | 一种亲水聚酯及其制备方法 |
| CN110467722B (zh) * | 2019-09-12 | 2021-11-30 | 武汉纺织大学 | 一种亲水聚酯及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61291622A (ja) | 1986-12-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR970002080B1 (ko) | 수용성 및/또는 수분산성 폴리에스테르의 제조방법 및 이들 폴리에스테르의 텍스타일 사(thread)의 사이징(sizing)에의 용도 | |
| US4427557A (en) | Anionic textile treating compositions | |
| DE4403866A1 (de) | Amphiphile Polyester, Verfahren zu ihrer Herstellung und ihre Verwendung in Waschmitteln | |
| WO2009063680A1 (fr) | Agent améliorant l'aptitude d'un matériau en fibre de polyester à être teint | |
| JPH0541745B2 (fr) | ||
| EP0066944A1 (fr) | Composition anionique pour le traitement de matières textiles | |
| WO2007132682A1 (fr) | Agent d'élimination d'oligomères pour matériau fibreux en polyester | |
| WO2003012024A1 (fr) | Composes de polyester sulfone a longue duree de conservation amelioree et methodes de production desdits composes | |
| JP4529048B2 (ja) | ポリエステル系処理剤及び該処理剤で処理された被処理品 | |
| JPH05230345A (ja) | 耐炎性ポリエステル | |
| BR112013019383B1 (pt) | Polímero linear de liberação de sujeira e líquido detergente alcalino | |
| JP3342578B2 (ja) | 脂肪族ポリエステルの製造方法 | |
| JPS633913B2 (fr) | ||
| US4043753A (en) | Grafting process for preparing a polyester fabric having desirable stain-release, antisoil-redeposition, antistatic and hydrophilic properties | |
| JPS6312897B2 (fr) | ||
| JPH0859808A (ja) | 脂肪族ポリエステルエーテル | |
| JP3706062B2 (ja) | ポリトリメチレンテレフタレート組成物及びその製造方法 | |
| JPH0568493B2 (fr) | ||
| JPH07276393A (ja) | コポリエーテルエステルから防水性で、水蒸気透過性の立体成形品を製造する方法 | |
| JP2003160648A (ja) | ポリトリメチレンテレフタレート組成物 | |
| JPS63256619A (ja) | 改質ポリエステルの製造法 | |
| US3439020A (en) | Process for purifying bis(beta-hydroxyethyl)terephthalate and isophthalate | |
| JP2766093B2 (ja) | ポリエステル弾性体及びその製造法 | |
| JPH072836B2 (ja) | 水分散性ポリエステル | |
| JPS61108768A (ja) | ポリエステル系合成繊維用処理剤 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| EXPY | Cancellation because of completion of term |