JP2010508393A - 熱可塑性エラストマーブレンド組成物 - Google Patents
熱可塑性エラストマーブレンド組成物 Download PDFInfo
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- JP2010508393A JP2010508393A JP2009534706A JP2009534706A JP2010508393A JP 2010508393 A JP2010508393 A JP 2010508393A JP 2009534706 A JP2009534706 A JP 2009534706A JP 2009534706 A JP2009534706 A JP 2009534706A JP 2010508393 A JP2010508393 A JP 2010508393A
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- Prior art keywords
- thermoplastic elastomer
- elastomer composition
- meth
- weight
- acrylate
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 103
- 229920002725 thermoplastic elastomer Polymers 0.000 title claims abstract description 43
- 229920001971 elastomer Polymers 0.000 claims abstract description 117
- 239000005060 rubber Substances 0.000 claims abstract description 59
- 239000000806 elastomer Substances 0.000 claims abstract description 58
- 229920000193 polymethacrylate Polymers 0.000 claims abstract description 28
- 238000004519 manufacturing process Methods 0.000 claims abstract description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 112
- -1 polytrimethylene Polymers 0.000 claims description 110
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 90
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 42
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims description 40
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims description 40
- 238000004132 cross linking Methods 0.000 claims description 37
- 150000002148 esters Chemical class 0.000 claims description 35
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 33
- 229920001577 copolymer Polymers 0.000 claims description 33
- 229920000642 polymer Polymers 0.000 claims description 33
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 32
- 239000002667 nucleating agent Substances 0.000 claims description 32
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 27
- 239000005977 Ethylene Substances 0.000 claims description 27
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 claims description 26
- 229920000573 polyethylene Polymers 0.000 claims description 22
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 19
- 239000004698 Polyethylene Substances 0.000 claims description 19
- 150000002009 diols Chemical class 0.000 claims description 19
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 15
- 239000000155 melt Substances 0.000 claims description 11
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- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical group C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 claims description 7
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
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- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
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- 239000011591 potassium Substances 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
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- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 68
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 229910052799 carbon Inorganic materials 0.000 description 21
- 239000012071 phase Substances 0.000 description 20
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 18
- 239000000463 material Substances 0.000 description 18
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- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 12
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- 239000011572 manganese Substances 0.000 description 10
- 229920000139 polyethylene terephthalate Polymers 0.000 description 9
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- 150000001991 dicarboxylic acids Chemical class 0.000 description 7
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 7
- 229920000728 polyester Polymers 0.000 description 7
- 239000004416 thermosoftening plastic Substances 0.000 description 7
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 239000012298 atmosphere Substances 0.000 description 6
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
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- 239000000376 reactant Substances 0.000 description 6
- 239000001488 sodium phosphate Substances 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 6
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 6
- 229920000800 acrylic rubber Polymers 0.000 description 5
- 125000005250 alkyl acrylate group Chemical group 0.000 description 5
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- LEJBBGNFPAFPKQ-UHFFFAOYSA-N 2-(2-prop-2-enoyloxyethoxy)ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOC(=O)C=C LEJBBGNFPAFPKQ-UHFFFAOYSA-N 0.000 description 4
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 230000003078 antioxidant effect Effects 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
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- ODBCKCWTWALFKM-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhex-3-yne Chemical compound CC(C)(C)OOC(C)(C)C#CC(C)(C)OOC(C)(C)C ODBCKCWTWALFKM-UHFFFAOYSA-N 0.000 description 3
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- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
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- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical class C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 238000003068 pathway analysis Methods 0.000 description 1
- ROTJZTYLACIJIG-UHFFFAOYSA-N pentane-1,3,5-tricarboxylic acid Chemical compound OC(=O)CCC(C(O)=O)CCC(O)=O ROTJZTYLACIJIG-UHFFFAOYSA-N 0.000 description 1
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- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
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- 235000011008 sodium phosphates Nutrition 0.000 description 1
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- 229910052712 strontium Inorganic materials 0.000 description 1
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- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
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- 238000009864 tensile test Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N tetraisopropyl titanate Substances CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
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- 229910052725 zinc Inorganic materials 0.000 description 1
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Classifications
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
- C08L67/025—Polyesters derived from dicarboxylic acids and dihydroxy compounds containing polyether sequences
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/10—Metal compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen
- C08L23/0869—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen with unsaturated acids, e.g. [meth]acrylic acid; with unsaturated esters, e.g. [meth]acrylic acid esters
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyesters Or Polycarbonates (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
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| US11/590,565 US7531593B2 (en) | 2006-10-31 | 2006-10-31 | Thermoplastic elastomer blend composition |
| PCT/US2007/022987 WO2008054776A1 (en) | 2006-10-31 | 2007-10-31 | Thermoplastic elastomer blend composition |
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| JP2010508393A true JP2010508393A (ja) | 2010-03-18 |
| JP2010508393A5 JP2010508393A5 (cg-RX-API-DMAC7.html) | 2010-11-25 |
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| JP (1) | JP2010508393A (cg-RX-API-DMAC7.html) |
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| CA (1) | CA2663814A1 (cg-RX-API-DMAC7.html) |
| DE (1) | DE112007002477T5 (cg-RX-API-DMAC7.html) |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011520012A (ja) * | 2008-05-07 | 2011-07-14 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | ポリ（トリメチレンエーテル）グリコールエステルを含む可塑剤 |
| KR101572449B1 (ko) * | 2013-12-10 | 2015-11-27 | 자동차부품연구원 | 열가소성 폴리에테르에스테르계 엘라스토머 조성물 및 이의 제조방법 |
| JP2022538103A (ja) * | 2019-06-27 | 2022-08-31 | アルケマ フランス | 熱可塑性エラストマーとフルオロポリマーの組合せ |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090246430A1 (en) | 2008-03-28 | 2009-10-01 | The Coca-Cola Company | Bio-based polyethylene terephthalate polymer and method of making same |
| US20100028512A1 (en) * | 2008-03-28 | 2010-02-04 | The Coca-Cola Company | Bio-based polyethylene terephthalate packaging and method of making thereof |
| CN101608056B (zh) * | 2008-06-17 | 2011-12-07 | E.I.内穆尔杜邦公司 | 热塑性弹性体组合物和制品 |
| JP5346207B2 (ja) * | 2008-12-05 | 2013-11-20 | 旭化成せんい株式会社 | ポリエーテルエステル及びポリエーテルエステル組成物 |
| CN102498086A (zh) | 2009-01-22 | 2012-06-13 | 阿迈瑞斯公司 | 产生十二烷二酸及其衍生物的方法 |
| PL2403894T3 (pl) | 2009-03-03 | 2016-12-30 | Opakowanie pochodzenia biologicznego z politereftalanu etylenu i sposób jego produkcji | |
| WO2010148070A2 (en) | 2009-06-16 | 2010-12-23 | Draths Corporation | Biobased polyesters |
| WO2010148080A2 (en) | 2009-06-16 | 2010-12-23 | Draths Corporation | Cyclohexane 1,4 carboxylates |
| WO2010148049A2 (en) | 2009-06-16 | 2010-12-23 | Draths Corporation | Preparation of trans, trans muconic acid and trans, trans muconates |
| WO2010148063A2 (en) | 2009-06-16 | 2010-12-23 | Draths Corporation | Cyclohexene 1,4-carboxylates |
| EP2443083A2 (en) | 2009-06-16 | 2012-04-25 | Amyris, Inc. | Cyclohexene 1,4-carboxylates |
| JP2013516196A (ja) | 2010-01-08 | 2013-05-13 | アミリス， インコーポレイテッド | ムコン酸およびムコン酸塩の異性体を生成するための方法 |
| CN102858816B (zh) * | 2010-04-26 | 2016-06-08 | 株式会社日本触媒 | 聚丙烯酸（盐）、聚丙烯酸（盐）系吸水性树脂及其制造方法 |
| JP5764122B2 (ja) * | 2010-04-26 | 2015-08-12 | 株式会社日本触媒 | ポリアクリル酸（塩）、ポリアクリル酸（塩）系吸水性樹脂及びその製造方法 |
| WO2012003461A2 (en) | 2010-07-02 | 2012-01-05 | Draths Corporation | Phloroglucinol synthases and methods of making and using the same |
| WO2012006245A1 (en) | 2010-07-06 | 2012-01-12 | Draths Corporation | Phloroglucinol reductase and methods of making and using the same |
| WO2012006244A1 (en) | 2010-07-06 | 2012-01-12 | Draths Corporation | Method for producing phloroglucinol and dihydrophloroglucinol |
| WO2012082727A1 (en) | 2010-12-15 | 2012-06-21 | Amyris, Inc. | Biobased polyamides |
| EP2686293A1 (en) | 2011-03-14 | 2014-01-22 | Dow Global Technologies LLC | Processes for producing terephthalic acid and terephthalic esters |
| US10128021B2 (en) * | 2013-03-18 | 2018-11-13 | Basf Se | Polyester for profile extrusion and/or pipe extrusion |
| CN107163509A (zh) * | 2017-06-13 | 2017-09-15 | 成都新三电线厂 | 环保型无卤高阻燃电缆 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5138392A (ja) * | 1974-09-30 | 1976-03-31 | Teijin Ltd | Shinjuyohyomenkotakujushi no seizoho |
| JPS5655451A (en) * | 1979-09-21 | 1981-05-16 | Ici Ltd | Quick crystallizable block copolyester composition |
| JPS63245427A (ja) * | 1987-03-31 | 1988-10-12 | Unitika Ltd | 耐衝撃性ポリエステル樹脂組成物 |
| JP2006501331A (ja) * | 2002-09-30 | 2006-01-12 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 硬化可能な熱可塑性エラストマーブレンド、その製造方法、およびその使用 |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3896078A (en) * | 1972-12-18 | 1975-07-22 | Du Pont | Stabilization of polymers containing poly(alkylene oxide) units |
| GB1603205A (en) | 1977-04-12 | 1981-11-18 | Raychem Ltd | Polymer compositions |
| EP0194808B1 (en) | 1985-03-08 | 1989-05-17 | Unitika Ltd. | Polyester resin composition for forming an impact resistant article |
| US4981908A (en) * | 1988-02-02 | 1991-01-01 | E. I. Du Pont De Nemours And Company | Thermoplastic elastomer blends |
| BR8901690A (pt) | 1988-04-11 | 1989-11-21 | Monsanto Co | Composicao elastomerica termoplastica e processo para reticular borracha com um composto com funcionalidade isocianato |
| DE3926136A1 (de) * | 1989-08-08 | 1991-02-14 | Degussa | Verfahren zur herstellung von 1,3-propandiol |
| DE4132663C2 (de) * | 1991-10-01 | 1993-10-14 | Degussa | Verfahren zum Herstellen von 1,3-Propandiol durch Hydrieren von Hydroxypropionaldehyd |
| DE4138981A1 (de) * | 1991-11-27 | 1993-06-03 | Degussa | Verfahren zur herstellung von 3-hydroxyalkanalen |
| DE4138982A1 (de) * | 1991-11-27 | 1993-06-03 | Degussa | Verfahren zur herstellung von 3-hydroxyalkanalen |
| DE4218282A1 (de) * | 1992-06-03 | 1993-12-09 | Degussa | Verfahren zur Herstellung von 1,3-Propandiol |
| DE4222708A1 (de) * | 1992-07-10 | 1994-01-13 | Degussa | Verfahren zur Herstellung von 1,3-Propandiol |
| US5633362A (en) * | 1995-05-12 | 1997-05-27 | E. I. Du Pont De Nemours And Company | Production of 1,3-propanediol from glycerol by recombinant bacteria expressing recombinant diol dehydratase |
| US5686276A (en) * | 1995-05-12 | 1997-11-11 | E. I. Du Pont De Nemours And Company | Bioconversion of a fermentable carbon source to 1,3-propanediol by a single microorganism |
| DE19703383A1 (de) * | 1997-01-30 | 1998-08-06 | Degussa | Verfahren zur Herstellung von 1,3-Propandiol |
| US5962745A (en) * | 1997-02-14 | 1999-10-05 | E. I. Du Pont De Nemours And Company | Process for preparing 3-hydroxyalkanals |
| KR20010013907A (ko) * | 1997-06-18 | 2001-02-26 | 메리 이. 보울러 | 3-히드록시프로피온알데히드의 수소화에 의한1,3-프로판디올의 제조 방법 |
| US6235948B1 (en) * | 1998-08-18 | 2001-05-22 | E. I. Du Pont De Nemours And Company | Process for the purification of 1,3-propanediol |
| KR20010073116A (ko) * | 1998-09-04 | 2001-07-31 | 메리 이. 보울러 | 3-히드록시프로판알의 촉매적 수소 첨가 반응에 의한1,3-프로판디올의 2-단계 제조 방법 |
| US6331264B1 (en) * | 1999-03-31 | 2001-12-18 | E. I. Du Pont De Nemours And Company | Low emission polymer compositions |
| US6277289B1 (en) * | 1999-07-01 | 2001-08-21 | E. I. Du Pont De Nemours And Company | Treatment of aqueous aldehyde waste streams |
| US6342646B1 (en) * | 1999-07-30 | 2002-01-29 | E. I. Du Pont De Nemours And Company | Catalytic hydrogenation of 3-hydroxypropanal to 1,3-propanediol |
| ATE326497T1 (de) * | 1999-12-17 | 2006-06-15 | Du Pont | Herstellung von polytrimethylene ether glycol und copolymere davon |
| CN1238317C (zh) * | 1999-12-17 | 2006-01-25 | 纳幕尔杜邦公司 | 制备聚三亚甲基醚二醇的连续方法 |
| US6528586B2 (en) * | 2000-05-16 | 2003-03-04 | Gordon Mark Cohen | Compositions of elastomeric ethylene/(meth)acrylic (acid) ester copolymer and polylactone or polyether |
| US20040030095A1 (en) * | 2002-08-09 | 2004-02-12 | Sunkara Hari B. | Poly(trimethylene-ethylene ether) glycols |
| US7323539B2 (en) * | 2003-05-06 | 2008-01-29 | E. I. Du Pont De Nemours And Company | Polytrimethylene ether glycol and polytrimethylene ether ester with excellent quality |
| BRPI0410686A (pt) * | 2003-05-06 | 2006-06-20 | Du Pont | processo e composição |
| US7084311B2 (en) * | 2003-05-06 | 2006-08-01 | E. I. Du Pont De Nemours And Company | Hydrogenation of chemically derived 1,3-propanediol |
| EP2239334A1 (en) * | 2003-05-06 | 2010-10-13 | E. I. du Pont de Nemours and Company | Purification of biologically-produced 1,3-propanediol |
| US7009082B2 (en) * | 2003-05-06 | 2006-03-07 | E.I. Du Pont De Nemours And Company | Removal of color bodies from polytrimethylene ether glycol polymers |
| US7153918B2 (en) * | 2003-07-24 | 2006-12-26 | E. I. Du Pont De Nemours And Company | Random ethylene/alkyl acrylate copolymers, compounds and elastomeric compositions thereof with improved low temperature properties |
| US7422795B2 (en) * | 2004-06-21 | 2008-09-09 | E.I. Du Pont De Nemours And Company | Polytrimethylene ether ester elastomer flexible films |
| US7244790B2 (en) * | 2005-05-02 | 2007-07-17 | E.I. Du Pont De Nemours And Company | Thermoplastic elastomer blend, method of manufacture and use thereof |
-
2006
- 2006-10-31 US US11/590,565 patent/US7531593B2/en not_active Expired - Fee Related
-
2007
- 2007-10-31 DE DE112007002477T patent/DE112007002477T5/de not_active Withdrawn
- 2007-10-31 JP JP2009534706A patent/JP2010508393A/ja active Pending
- 2007-10-31 CA CA002663814A patent/CA2663814A1/en not_active Abandoned
- 2007-10-31 KR KR1020097011077A patent/KR20090088383A/ko not_active Withdrawn
- 2007-10-31 CN CN2007800408413A patent/CN101535403B/zh not_active Expired - Fee Related
- 2007-10-31 WO PCT/US2007/022987 patent/WO2008054776A1/en not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5138392A (ja) * | 1974-09-30 | 1976-03-31 | Teijin Ltd | Shinjuyohyomenkotakujushi no seizoho |
| JPS5655451A (en) * | 1979-09-21 | 1981-05-16 | Ici Ltd | Quick crystallizable block copolyester composition |
| JPS63245427A (ja) * | 1987-03-31 | 1988-10-12 | Unitika Ltd | 耐衝撃性ポリエステル樹脂組成物 |
| JP2006501331A (ja) * | 2002-09-30 | 2006-01-12 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 硬化可能な熱可塑性エラストマーブレンド、その製造方法、およびその使用 |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011520012A (ja) * | 2008-05-07 | 2011-07-14 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | ポリ（トリメチレンエーテル）グリコールエステルを含む可塑剤 |
| KR101572449B1 (ko) * | 2013-12-10 | 2015-11-27 | 자동차부품연구원 | 열가소성 폴리에테르에스테르계 엘라스토머 조성물 및 이의 제조방법 |
| JP2022538103A (ja) * | 2019-06-27 | 2022-08-31 | アルケマ フランス | 熱可塑性エラストマーとフルオロポリマーの組合せ |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2663814A1 (en) | 2008-05-08 |
| WO2008054776A1 (en) | 2008-05-08 |
| US20080103243A1 (en) | 2008-05-01 |
| CN101535403B (zh) | 2012-01-04 |
| CN101535403A (zh) | 2009-09-16 |
| KR20090088383A (ko) | 2009-08-19 |
| DE112007002477T5 (de) | 2009-09-10 |
| US7531593B2 (en) | 2009-05-12 |
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