JP2004149692A5 - - Google Patents

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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
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acid
acid amide
resin composition
weight
composition according
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JP2002317450A
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JP2004149692A (en
JP3988619B2 (en
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(耐折回数)
厚さ約250μmのシートを用い、MIT耐揉疲労試験機((株)東洋精機製作所)により、JIS P−8115に基づいて測定した。尚、耐折強さは耐折回数の常用対数である。
(Number of folds)
Using a sheet with a thickness of about 250 μm, the sheet was measured according to JIS P-8115 using a MIT corrosion resistant fatigue tester (manufactured by Toyo Seiki Seisakusho Co., Ltd.). The folding resistance is a common logarithm of the number of foldings.

製造例2〜11(乳酸系ポリエステルP−2〜P−11の合成)
ジカルボン酸、ジオール、ラクタイドの種類、添加量を表1のように変えた以外は、製造例1と同様にして、乳酸系ポリエステル(P−2〜P−11)を合成した。
各ポリマーの数平均分子量(Mn)、重量平均分子量(Mw)、ガラス転移点(Tg)についても表1〜3に示す。
Production Examples 2 to 11 (Synthesis of Lactic Acid-Based Polyester P-2 to P-11)
A lactic acid-based polyester (P-2 to P-11) was synthesized in the same manner as in Production Example 1 except that the kind of dicarboxylic acid, diol, and lactide and the addition amount thereof were changed as shown in Table 1.
The number average molecular weight (Mn), weight average molecular weight (Mw), and glass transition point (Tg) of each polymer are also shown in Tables 1 to 3.

一方、比較例においては、乳酸系ポリエステル及び透明核剤を添加しない場合は耐折回数は0回と堅くて脆く、また耐熱性が低い成形品しか得られない(比較例1)。また、乳酸系ポリエステルを添加しない場合は、耐熱性のある成形品が得られるが、耐折回数は回と、樹脂の脆さは改善されていない(比較例2)。さらに、透明結晶核剤を添加しない場合は、耐折回数は500回以上と脆さは改善されているが、耐熱性のある成形品は得られない(比較例3)。 On the other hand, in the comparative example, when the lactic acid-based polyester and the transparent nucleating agent are not added, only a molded product having a low number of folds, which is hard and brittle with zero folding resistance, is obtained (Comparative Example 1). In addition, when a lactic acid-based polyester is not added, a heat-resistant molded article is obtained, but the number of times of folding is three, and the brittleness of the resin is not improved (Comparative Example 2). Furthermore, when the transparent crystal nucleating agent is not added, although the number of times of folding is improved to 500 or more and the brittleness is improved, a heat-resistant molded article can not be obtained (Comparative Example 3).

Claims (8)

乳酸成分(I)とポリエステル成分(II)を重量比で10:90〜90:10の範囲で有する乳酸系ポリエステル及びポリ乳酸からなる高分子成分100重量部に対して、脂肪族カルボン酸アミド、脂肪族カルボン酸塩、脂肪族アルコール及び脂肪族カルボン酸エステルからなる化合物群から選択された少なくとも一種を0.1〜5重量部含むことを特徴とするポリ乳酸系樹脂組成物。Aliphatic carboxylic acid amide with respect to 100 parts by weight of a polymer component consisting of a lactic acid-based polyester having a lactic acid component (I) and a polyester component (II) in a weight ratio in the range of 10:90 to 90:10; A polylactic acid-based resin composition comprising 0.1 to 5 parts by weight of at least one selected from the group consisting of aliphatic carboxylic acid salts, aliphatic alcohols and aliphatic carboxylic acid esters. 該高分子成分中のポリ乳酸の含有率が高々99重量%である、請求項1記載のポリ乳酸系樹脂組成物。  The polylactic acid-based resin composition according to claim 1, wherein the content of polylactic acid in the polymer component is at most 99% by weight. 乳酸系ポリエステルが乳酸成分(I)と、ジカルボン酸(IIa)及びジオール(IIb)からなるポリエステル成分(II)とを重量比で10:90〜90:10の範囲で反応させた反応生成物である請求項1又は2に記載のポリ乳酸系樹脂組成物。  A reaction product obtained by reacting a lactic acid-based polyester with a lactic acid component (I) and a polyester component (II) consisting of a dicarboxylic acid (IIa) and a diol (IIb) in a weight ratio of 10:90 to 90:10. The polylactic acid-based resin composition according to claim 1 or 2. 脂肪族カルボン酸アミド、脂肪族カルボン酸塩、脂肪族アルコール及び脂肪族カルボン酸エステルからなる化合物群から選択された少なくとも一種がパルミチン酸アミド、ステアリン酸アミド、エルカ酸アミド、べヘニン酸アミド、リシノール酸アミド、ヒドロキシステアリン酸アミド、N−オレイルパルミチン酸アミド、N−ステアリルエルカ酸アミド、エチレンビスカプリン酸アミド、エチレンビスラウリン酸アミド、エチレンビスエルカ酸アミド、エチレンビスオレイン酸アミド、m−キシリレンビスステアリン酸アミド、m−キシリレンビス−12−ヒドロキシステアリン酸アミド、ステアリン酸ナトリウム、ステアリン酸カリウム、ステアリン酸亜鉛、モンタン酸カルシウム、エチレングリコールジステアレート及びステアリルアルコール、からなる群から選択された少なくとも一種である請求項1〜3いずれかに記載のポリ乳酸系樹脂組成物。  At least one selected from the compound group consisting of aliphatic carboxylic acid amide, aliphatic carboxylic acid salt, aliphatic alcohol and aliphatic carboxylic acid ester is palmitic acid amide, stearic acid amide, erucic acid amide, behenic acid amide, ricinol Acid amide, hydroxystearic acid amide, N-oleyl palmitic acid amide, N-stearyl erucic acid amide, ethylene bis capric acid amide, ethylene bis lauric acid amide, ethylene bis erucic acid amide, ethylene bis oleic acid amide, m-xylylene Bisstearic acid amide, m-xylylene bis-12-hydroxystearic acid amide, sodium stearate, potassium stearate, zinc stearate, calcium montanate, ethylene glycol distearate and stearyla Call, polylactic acid resin composition according to any one of claims 1 to 3 is at least one selected from the group consisting of. ジカルボン酸(IIa)の合計量に対する脂肪族ジカルボン酸の割合が30〜100重量%の範囲にあり、かつ、ジオール(IIb)の合計量に対する脂肪族ジオールの割合が40〜100重量%の範囲にある請求項1〜4いずれかに記載のポリ乳酸系樹脂組成物。  The ratio of aliphatic dicarboxylic acid to the total amount of dicarboxylic acid (IIa) is in the range of 30 to 100% by weight, and the ratio of aliphatic diol to the total amount of diol (IIb) in the range of 40 to 100% by weight The polylactic acid-based resin composition according to any one of claims 1 to 4. 厚み0.3mmの成形品のヘイズ値が15%以下であり、かつ、示差走査熱量計で200℃から10℃/分の速度で降温したときに、樹脂の結晶化に伴う発熱ピークが測定されることを特徴とする請求項1〜5いずれかに記載のポリ乳酸系樹脂組成物。  When the haze value of a 0.3 mm-thick molded article is 15% or less and the temperature is lowered at a rate of 200 ° C. to 10 ° C./min with a differential scanning calorimeter, an exothermic peak accompanying crystallization of the resin is measured The polylactic acid-based resin composition according to any one of claims 1 to 5, characterized in that 請求項1〜6のいずれかに記載のポリ乳酸系樹脂組成物よりなり、厚み0.3mmの成形品のヘイズ値が20%以下であり、示差走査熱量計で0℃から融点まで10℃/分の速度で昇温したときに測定される、樹脂の結晶化に伴う発熱量が15J/g以下であることを特徴とする成形品。  A haze value of a molded article having a thickness of 0.3 mm comprising a polylactic acid-based resin composition according to any one of claims 1 to 20 is 20% or less, and a differential scanning calorimeter from 0 ° C to a melting point of 10 ° C / A molded article characterized by having a calorific value accompanying crystallization of a resin of 15 J / g or less, which is measured when the temperature is raised at a speed of a minute. 形態がシート状である請求項7に記載の成形品。  The molded article according to claim 7, which is in the form of a sheet.
JP2002317450A 2002-10-31 2002-10-31 Polylactic acid resin composition and molded article comprising the same Expired - Fee Related JP3988619B2 (en)

Priority Applications (1)

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JP2004149692A JP2004149692A (en) 2004-05-27
JP2004149692A5 true JP2004149692A5 (en) 2005-06-09
JP3988619B2 JP3988619B2 (en) 2007-10-10

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JP4576166B2 (en) * 2004-06-22 2010-11-04 三菱樹脂株式会社 Injection molded body
JP2006070057A (en) * 2004-08-31 2006-03-16 Dainippon Ink & Chem Inc Crystalline polylactic acid resin composition and film obtained using the same
US7301000B2 (en) 2004-09-15 2007-11-27 The Procter & Gamble Company Nucleating agents for polyhydroxyalkanoates
US20090082499A1 (en) * 2004-11-16 2009-03-26 Mitsubishi Plastics, Inc. Aliphatic polyester-based resin reflective film and reflective plate
TW201005393A (en) * 2004-11-19 2010-02-01 Mitsubishi Plastics Inc Light reflecting body and manufacturing method of light reflecting body
JP2007023076A (en) * 2005-07-12 2007-02-01 Mitsui Chemicals Inc Flame-retardant resin composition
US8431212B2 (en) 2005-08-31 2013-04-30 Toray Industries, Inc. Laminate sheet of polylactic acid-based resin and thermoformed plastic thereof
EP2045293B1 (en) 2006-07-26 2013-09-04 Mitsui Chemicals, Inc. Polylactic acid resin composition and molded body thereof
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 (en) * 2008-09-16 2013-10-23 東レ株式会社 Polyester film
JP5873317B2 (en) * 2011-12-14 2016-03-01 株式会社クレハ Antibacterial nonwoven fabric formed from biodegradable aliphatic polyester fiber and antibacterial method
US9480588B2 (en) 2014-08-15 2016-11-01 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
US9730819B2 (en) 2014-08-15 2017-08-15 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
EP3861961A1 (en) 2016-05-16 2021-08-11 Elixir Medical Corporation Uncaging stent
US11622872B2 (en) 2016-05-16 2023-04-11 Elixir Medical Corporation Uncaging stent
CN111303600B (en) * 2020-04-24 2021-07-06 中国科学技术大学 Polylactic acid/Zn2+Heat-resistant composite material and preparation method thereof
CN114805982B (en) * 2022-04-18 2023-08-18 嘉应学院 Luminescent material and preparation method thereof

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