JP2004149692A5 - - Google Patents
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- Publication number
- JP2004149692A5 JP2004149692A5 JP2002317450A JP2002317450A JP2004149692A5 JP 2004149692 A5 JP2004149692 A5 JP 2004149692A5 JP 2002317450 A JP2002317450 A JP 2002317450A JP 2002317450 A JP2002317450 A JP 2002317450A JP 2004149692 A5 JP2004149692 A5 JP 2004149692A5
- Authority
- JP
- Japan
- Prior art keywords
- acid
- acid amide
- resin composition
- weight
- composition according
- 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.)
- Granted
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- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 14
- 229920000728 polyester Polymers 0.000 claims description 8
- 235000014655 lactic acid Nutrition 0.000 claims description 7
- 239000004310 lactic acid Substances 0.000 claims description 7
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 6
- 150000002009 diols Chemical class 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000011347 resin Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- 229920000747 poly(lactic acid) Polymers 0.000 claims 8
- 239000004626 polylactic acid Substances 0.000 claims 8
- 239000011342 resin composition Substances 0.000 claims 7
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 6
- -1 aliphatic alcohols Chemical class 0.000 claims 3
- 238000002425 crystallisation Methods 0.000 claims 2
- 230000008025 crystallization Effects 0.000 claims 2
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 claims 2
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims 1
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- 229940114072 12-hydroxystearic acid Drugs 0.000 claims 1
- RDYWHMBYTHVOKZ-UHFFFAOYSA-N 18-hydroxyoctadecanamide Chemical compound NC(=O)CCCCCCCCCCCCCCCCCO RDYWHMBYTHVOKZ-UHFFFAOYSA-N 0.000 claims 1
- XHSVWKJCURCWFU-UHFFFAOYSA-N 19-[3-(19-amino-19-oxononadecyl)phenyl]nonadecanamide Chemical compound NC(=O)CCCCCCCCCCCCCCCCCCC1=CC=CC(CCCCCCCCCCCCCCCCCCC(N)=O)=C1 XHSVWKJCURCWFU-UHFFFAOYSA-N 0.000 claims 1
- ORAWFNKFUWGRJG-UHFFFAOYSA-N Docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(N)=O ORAWFNKFUWGRJG-UHFFFAOYSA-N 0.000 claims 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- FPVVYTCTZKCSOJ-UHFFFAOYSA-N Ethylene glycol distearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(=O)CCCCCCCCCCCCCCCCC FPVVYTCTZKCSOJ-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- FIASKJZPIYCESA-UHFFFAOYSA-L calcium;octacosanoate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCCCCCCCC([O-])=O FIASKJZPIYCESA-UHFFFAOYSA-L 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 150000001875 compounds Chemical group 0.000 claims 1
- GKAWAQNIMXHVNI-UHFFFAOYSA-N decanamide;ethene Chemical compound C=C.CCCCCCCCCC(N)=O.CCCCCCCCCC(N)=O GKAWAQNIMXHVNI-UHFFFAOYSA-N 0.000 claims 1
- GFQOFGWPGYRLAO-UHFFFAOYSA-N dodecanamide;ethene Chemical compound C=C.CCCCCCCCCCCC(N)=O.CCCCCCCCCCCC(N)=O GFQOFGWPGYRLAO-UHFFFAOYSA-N 0.000 claims 1
- SWSBIGKFUOXRNJ-CVBJKYQLSA-N ethene;(z)-octadec-9-enamide Chemical compound C=C.CCCCCCCC\C=C/CCCCCCCC(N)=O.CCCCCCCC\C=C/CCCCCCCC(N)=O SWSBIGKFUOXRNJ-CVBJKYQLSA-N 0.000 claims 1
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical group CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- VMRGZRVLZQSNHC-ZCXUNETKSA-N n-[(z)-octadec-9-enyl]hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(=O)NCCCCCCCC\C=C/CCCCCCCC VMRGZRVLZQSNHC-ZCXUNETKSA-N 0.000 claims 1
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 claims 1
- 229940114930 potassium stearate Drugs 0.000 claims 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 claims 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 claims 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims 1
- 230000000052 comparative effect Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000003484 crystal nucleating agent Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002317450A JP3988619B2 (ja) | 2002-10-31 | 2002-10-31 | ポリ乳酸系樹脂組成物およびそれからなる成形品 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002317450A JP3988619B2 (ja) | 2002-10-31 | 2002-10-31 | ポリ乳酸系樹脂組成物およびそれからなる成形品 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2004149692A JP2004149692A (ja) | 2004-05-27 |
JP2004149692A5 true JP2004149692A5 (enrdf_load_stackoverflow) | 2005-06-09 |
JP3988619B2 JP3988619B2 (ja) | 2007-10-10 |
Family
ID=32460848
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2002317450A Expired - Fee Related JP3988619B2 (ja) | 2002-10-31 | 2002-10-31 | ポリ乳酸系樹脂組成物およびそれからなる成形品 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3988619B2 (enrdf_load_stackoverflow) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4576166B2 (ja) * | 2004-06-22 | 2010-11-04 | 三菱樹脂株式会社 | 射出成形体 |
JP2006070057A (ja) * | 2004-08-31 | 2006-03-16 | Dainippon Ink & Chem Inc | 結晶性ポリ乳酸樹脂組成物及びそれを用いて得られるフィルム |
US7301000B2 (en) | 2004-09-15 | 2007-11-27 | The Procter & Gamble Company | Nucleating agents for polyhydroxyalkanoates |
WO2006054475A1 (ja) * | 2004-11-16 | 2006-05-26 | Mitsubishi Plastics, Inc. | 脂肪族ポリエステル系樹脂反射フィルム及び反射板 |
TW200628296A (en) * | 2004-11-19 | 2006-08-16 | Mitsubishi Plastics Inc | Light reflecting body and manufacturing method of light reflecting body |
JP2007023076A (ja) * | 2005-07-12 | 2007-02-01 | Mitsui Chemicals Inc | 難燃樹脂組成物 |
JP5162900B2 (ja) | 2005-08-31 | 2013-03-13 | 東レ株式会社 | ポリ乳酸系樹脂積層シートおよびその成形体 |
JP5404040B2 (ja) | 2006-07-26 | 2014-01-29 | 三井化学株式会社 | ポリ乳酸系樹脂組成物およびその成形体 |
US20080177373A1 (en) * | 2007-01-19 | 2008-07-24 | Elixir Medical Corporation | Endoprosthesis structures having supporting features |
US8814930B2 (en) | 2007-01-19 | 2014-08-26 | Elixir Medical Corporation | Biodegradable endoprosthesis and methods for their fabrication |
JP5320920B2 (ja) * | 2008-09-16 | 2013-10-23 | 東レ株式会社 | ポリエステルフィルム |
JP5873317B2 (ja) * | 2011-12-14 | 2016-03-01 | 株式会社クレハ | 生分解性脂肪族ポリエステル繊維から形成される抗菌性不織布、及び抗菌方法 |
US9730819B2 (en) | 2014-08-15 | 2017-08-15 | Elixir Medical Corporation | Biodegradable endoprostheses and methods of their fabrication |
US9855156B2 (en) | 2014-08-15 | 2018-01-02 | Elixir Medical Corporation | Biodegradable endoprostheses and methods of their fabrication |
US9480588B2 (en) | 2014-08-15 | 2016-11-01 | Elixir Medical Corporation | Biodegradable endoprostheses and methods of their fabrication |
US9259339B1 (en) | 2014-08-15 | 2016-02-16 | Elixir Medical Corporation | Biodegradable endoprostheses and methods of their fabrication |
US11622872B2 (en) | 2016-05-16 | 2023-04-11 | Elixir Medical Corporation | Uncaging stent |
EP3457985B1 (en) | 2016-05-16 | 2021-02-17 | Elixir Medical Corporation | Uncaging stent |
CN111303600B (zh) * | 2020-04-24 | 2021-07-06 | 中国科学技术大学 | 一种聚乳酸/Zn2+耐热复合材料及其制备方法 |
US20230146000A1 (en) | 2020-10-05 | 2023-05-11 | Lg Chem, Ltd. | Copolymer and preparation method thereof |
CN114805982B (zh) * | 2022-04-18 | 2023-08-18 | 嘉应学院 | 一种发光材料及其制备方法 |
-
2002
- 2002-10-31 JP JP2002317450A patent/JP3988619B2/ja not_active Expired - Fee Related
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