JP2011505433A5 - - Google Patents
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- Publication number
- JP2011505433A5 JP2011505433A5 JP2010532223A JP2010532223A JP2011505433A5 JP 2011505433 A5 JP2011505433 A5 JP 2011505433A5 JP 2010532223 A JP2010532223 A JP 2010532223A JP 2010532223 A JP2010532223 A JP 2010532223A JP 2011505433 A5 JP2011505433 A5 JP 2011505433A5
- Authority
- JP
- Japan
- Prior art keywords
- acid
- composition
- poly
- article
- hydroxyalkanoic
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 claims description 30
- 239000002253 acid Substances 0.000 claims description 15
- 239000003607 modifier Substances 0.000 claims description 5
- 239000002667 nucleating agent Substances 0.000 claims description 5
- 239000004609 Impact Modifier Substances 0.000 claims description 4
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 claims description 3
- OXSSIXNFGTZQMZ-UHFFFAOYSA-N 3-hydroxyheptanoic acid Chemical compound CCCCC(O)CC(O)=O OXSSIXNFGTZQMZ-UHFFFAOYSA-N 0.000 claims description 2
- HPMGFDVTYHWBAG-UHFFFAOYSA-N 3-hydroxyhexanoic acid Chemical compound CCCC(O)CC(O)=O HPMGFDVTYHWBAG-UHFFFAOYSA-N 0.000 claims description 2
- IWHLYPDWHHPVAA-UHFFFAOYSA-N 6-hydroxyhexanoic acid Chemical compound OCCCCCC(O)=O IWHLYPDWHHPVAA-UHFFFAOYSA-N 0.000 claims description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 2
- ABIKNKURIGPIRJ-UHFFFAOYSA-N DL-4-hydroxy caproic acid Chemical compound CCC(O)CCC(O)=O ABIKNKURIGPIRJ-UHFFFAOYSA-N 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 2
- 238000001746 injection moulding Methods 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 2
- 238000003856 thermoforming Methods 0.000 claims description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 3
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 2
- PLHAOKZSDZWIBV-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate;oxiran-2-ylmethyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C=C.CC(=C)C(=O)OCC1CO1 PLHAOKZSDZWIBV-UHFFFAOYSA-N 0.000 description 2
- WHBMMWSBFZVSSR-UHFFFAOYSA-N 3-hydroxybutyric acid Chemical compound CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 description 2
- REKYPYSUBKSCAT-UHFFFAOYSA-N 3-hydroxypentanoic acid Chemical compound CCC(O)CC(O)=O REKYPYSUBKSCAT-UHFFFAOYSA-N 0.000 description 2
- ALRHLSYJTWAHJZ-UHFFFAOYSA-N 3-hydroxypropionic acid Chemical compound OCCC(O)=O ALRHLSYJTWAHJZ-UHFFFAOYSA-N 0.000 description 2
- FMHKPLXYWVCLME-UHFFFAOYSA-N 4-hydroxy-valeric acid Chemical compound CC(O)CCC(O)=O FMHKPLXYWVCLME-UHFFFAOYSA-N 0.000 description 2
- SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical compound OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 0.000 description 2
- 229930182556 Polyacetal Natural products 0.000 description 2
- YEIJWBZJZKCVTA-UHFFFAOYSA-N butyl prop-2-enoate;oxiran-2-ylmethyl 2-methylprop-2-enoate Chemical compound CCCCOC(=O)C=C.CC(=C)C(=O)OCC1CO1 YEIJWBZJZKCVTA-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- MZLCVCICBVBUFJ-UHFFFAOYSA-N ethyl prop-2-enoate;oxiran-2-ylmethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C=C.CC(=C)C(=O)OCC1CO1 MZLCVCICBVBUFJ-UHFFFAOYSA-N 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920000747 poly(lactic acid) Polymers 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- AFENDNXGAFYKQO-VKHMYHEASA-N (S)-2-hydroxybutyric acid Chemical compound CC[C@H](O)C(O)=O AFENDNXGAFYKQO-VKHMYHEASA-N 0.000 description 1
- LMAUULKNZLEMGN-UHFFFAOYSA-N 1-ethyl-3,5-dimethylbenzene Chemical compound CCC1=CC(C)=CC(C)=C1 LMAUULKNZLEMGN-UHFFFAOYSA-N 0.000 description 1
- KZDCPJDWDXMJRA-UHFFFAOYSA-N 2-hydroxybutanoic acid;pentanoic acid Chemical compound CCCCC(O)=O.CCC(O)C(O)=O KZDCPJDWDXMJRA-UHFFFAOYSA-N 0.000 description 1
- JRHWHSJDIILJAT-UHFFFAOYSA-N 2-hydroxypentanoic acid Chemical compound CCCC(O)C(O)=O JRHWHSJDIILJAT-UHFFFAOYSA-N 0.000 description 1
- 229940006015 4-hydroxybutyric acid Drugs 0.000 description 1
- PHOJOSOUIAQEDH-UHFFFAOYSA-N 5-hydroxypentanoic acid Chemical compound OCCCCC(O)=O PHOJOSOUIAQEDH-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920000954 Polyglycolide Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US98396507P | 2007-10-31 | 2007-10-31 | |
| PCT/US2008/081663 WO2009058920A1 (en) | 2007-10-31 | 2008-10-30 | Poly(hydroxyalkanoic acid) composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2011505433A JP2011505433A (ja) | 2011-02-24 |
| JP2011505433A5 true JP2011505433A5 (enExample) | 2011-12-15 |
Family
ID=40210850
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010532223A Pending JP2011505433A (ja) | 2007-10-31 | 2008-10-30 | ポリ（ヒドロキシアルカン酸）組成物 |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US20090110859A1 (enExample) |
| JP (1) | JP2011505433A (enExample) |
| WO (1) | WO2009058920A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5973132B2 (ja) * | 2007-10-01 | 2016-08-23 | アーケマ・インコーポレイテッド | 生分解性ポリマーとアクリル系共重合体とのブレンド |
| US20110028622A1 (en) * | 2009-07-28 | 2011-02-03 | E. I. Du Pont De Nemours And Company | Poly(hydroxyalkanoic acid) blown film |
| WO2011043676A1 (en) * | 2009-10-07 | 2011-04-14 | Auckland Uniservices Limited | Reactive polymeric mixture |
| CN102020746A (zh) * | 2010-11-09 | 2011-04-20 | 长春工业大学 | 一种环氧官能化丙烯酸酯类聚合物的应用 |
| CN102030861B (zh) * | 2010-11-09 | 2012-12-05 | 长春工业大学 | 一种环氧官能化丙烯酸酯类聚合物的制备方法 |
| JP5852375B2 (ja) * | 2011-09-07 | 2016-02-03 | 麒麟麦酒株式会社 | ガスバリア性ポリ乳酸樹脂成形体 |
| EP2855556A4 (en) * | 2012-05-25 | 2016-02-10 | Polyone Corp | OXYGEN ABSORBING COPOLYMERS FROM CYCLIC ALIPHATIC MONOMERS |
| CN103113533B (zh) * | 2013-02-01 | 2015-08-05 | 中国科学院长春应用化学研究所 | 聚乳酸共聚物及其制备方法、改性聚乳酸 |
| US10589455B2 (en) * | 2014-11-25 | 2020-03-17 | Polymer Technologies, Inc. | Foam insulation with thermoformable film coating and process for manufacture |
| CN114989583A (zh) * | 2022-05-20 | 2022-09-02 | 北京蓝晶微生物科技有限公司 | 聚羟基烷酸酯的酸类成核剂及聚羟基烷酸酯成型体 |
| CN117209980B (zh) * | 2023-05-29 | 2024-04-30 | 北京蓝晶微生物科技有限公司 | 一种聚羟基脂肪酸酯组合物、聚羟基脂肪酸酯成型体及其制备方法 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991009909A1 (en) * | 1989-12-27 | 1991-07-11 | Polysar Financial Services S.A. | Polymeric composition having orthopedic utility |
| JPH0623836A (ja) * | 1992-07-09 | 1994-02-01 | Shimadzu Corp | ポリ乳酸延伸フィルムの製造方法 |
| US6417294B1 (en) * | 1995-12-21 | 2002-07-09 | Mitsui Chemicals, Inc. | Films and molded articles formed from aliphatic polyester compositions containing nucleating agents |
| US6114495A (en) * | 1998-04-01 | 2000-09-05 | Cargill Incorporated | Lactic acid residue containing polymer composition and product having improved stability, and method for preparation and use thereof |
| DE60007789T2 (de) * | 1999-03-26 | 2004-11-04 | Toyo Boseki K.K. | Folie aus Polymilchsäure |
| JP3236842B2 (ja) * | 1999-10-27 | 2001-12-10 | 三菱樹脂株式会社 | 生分解性袋 |
| EP1188781B1 (en) * | 2000-03-22 | 2008-01-23 | Dainippon Ink And Chemicals, Inc. | Impact modifier and polyester composition containing the modifier |
| KR100840219B1 (ko) * | 2001-08-03 | 2008-06-23 | 도레이 가부시끼가이샤 | 수지 조성물 및 그것으로 이루어진 성형품, 필름 및 섬유 |
| WO2003037966A1 (en) * | 2001-11-01 | 2003-05-08 | Asahi Kasei Life & Living Corporation | Biaxially oriented polylactic acid-based resin films |
| JP5177931B2 (ja) * | 2002-01-24 | 2013-04-10 | 東レ株式会社 | 脂肪族ポリエステル樹脂組成物およびそれからなる成形品 |
| JP4232377B2 (ja) * | 2002-03-28 | 2009-03-04 | 東レ株式会社 | ポリ乳酸含有樹脂組成物、それからなる成形品、および、フィルムまたはシート |
| US6943214B2 (en) * | 2003-05-13 | 2005-09-13 | E. I. Du Pont De Nemours And Company | Toughened polyoxymethylene-poly(lactic acid) compositions |
| US7354973B2 (en) * | 2003-12-12 | 2008-04-08 | E.I. Du Pont De Nemours And Company | Toughened poly(lactic acid) compositions |
| US20080027178A1 (en) * | 2006-07-27 | 2008-01-31 | Julius Uradnisheck | Article comprising poly(hydroxyalkanoic acid) |
| US7595363B2 (en) * | 2003-12-12 | 2009-09-29 | E.I. Du Pont De Nemours And Company | Toughened poly(hydroxyalkanoic acid) compositions |
| US7368503B2 (en) * | 2003-12-22 | 2008-05-06 | Eastman Chemical Company | Compatibilized blends of biodegradable polymers with improved rheology |
| JP2005232230A (ja) * | 2004-02-17 | 2005-09-02 | Tosoh Corp | 樹脂組成物 |
| TW200706594A (en) * | 2005-05-09 | 2007-02-16 | Kaneka Corp | Biodegradable resin composition and molded article produced from the same |
| CN101175818B (zh) * | 2005-05-13 | 2011-06-22 | 株式会社钟化 | 生物降解性树脂组合物及其成型体 |
| JP2006328117A (ja) * | 2005-05-23 | 2006-12-07 | National Institute Of Advanced Industrial & Technology | 耐衝撃性環境素材とその製造方法及び成形体 |
| US8399101B2 (en) * | 2006-09-19 | 2013-03-19 | E I Du Pont De Nemours And Company | Toughened poly(hydroxyalkanoic acid) compositions |
| JP2010504396A (ja) * | 2006-09-19 | 2010-02-12 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 強化ポリ（ヒドロキシアルカン酸）組成物 |
| JP2008106254A (ja) * | 2006-09-27 | 2008-05-08 | Kaneka Corp | 樹脂組成物 |
| JP5509517B2 (ja) * | 2007-03-09 | 2014-06-04 | 東レ株式会社 | 樹脂組成物およびそれからなる成形品 |
| CN101338069B (zh) * | 2008-08-11 | 2011-05-04 | 中国科学院长春应用化学研究所 | 一种完全生物降解增韧型聚乳酸树脂及制备方法 |
| CN102093682B (zh) * | 2010-12-28 | 2013-01-30 | 奇瑞汽车股份有限公司 | 一种轻质聚乳酸复合材料及其制备方法 |
-
2008
- 2008-10-30 JP JP2010532223A patent/JP2011505433A/ja active Pending
- 2008-10-30 WO PCT/US2008/081663 patent/WO2009058920A1/en not_active Ceased
- 2008-10-31 US US12/262,720 patent/US20090110859A1/en not_active Abandoned
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