CN101338069A - 一种完全生物降解增韧型聚乳酸树脂及制备方法 - Google Patents

一种完全生物降解增韧型聚乳酸树脂及制备方法 Download PDF

Info

Publication number
CN101338069A
CN101338069A CNA2008100510649A CN200810051064A CN101338069A CN 101338069 A CN101338069 A CN 101338069A CN A2008100510649 A CNA2008100510649 A CN A2008100510649A CN 200810051064 A CN200810051064 A CN 200810051064A CN 101338069 A CN101338069 A CN 101338069A
Authority
CN
China
Prior art keywords
massfraction
toughner
toughener
complete
oxidation inhibitor
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
Application number
CNA2008100510649A
Other languages
English (en)
Other versions
CN101338069B (zh
Inventor
刘南安
姚彬
冉祥海
董丽松
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jilin Kaishun New Material Co ltd
Original Assignee
Changchun Institute of Applied Chemistry of CAS
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Changchun Institute of Applied Chemistry of CAS filed Critical Changchun Institute of Applied Chemistry of CAS
Priority to CN2008100510649A priority Critical patent/CN101338069B/zh
Publication of CN101338069A publication Critical patent/CN101338069A/zh
Application granted granted Critical
Publication of CN101338069B publication Critical patent/CN101338069B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Tires In General (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Biological Depolymerization Polymers (AREA)

Abstract

本发明涉及一种完全生物降解增韧型聚乳酸树脂的制备方法。聚乳酸基础树脂、增韧剂和抗氧剂在60℃烘箱中干燥,然后在橡塑混炼机上密炼,工艺温度180℃,转速40转/分,时间5分钟,得到一种完全生物降解增韧型聚乳酸树脂。乳酸基与增韧剂具有较好的相容性,可按任意比例进行混合;增韧剂成本低,混合后可减低成本;原材料无毒无害,产品应用安全卫生;适当调整增韧剂单体配比和增韧剂用量,在较宽的范围内都会得到性能优良的增韧材料。所得产物可用于制备薄膜、板材、片材、发泡和注塑成型塑料件。

Description

一种完全生物降解增韧型聚乳酸树脂及制备方法
技术领域
本发明属于一种完全生物降解增韧型聚乳酸树脂及制备方法。
背景技术
改善聚乳酸(PLA)的柔韧性能一直是将PLA推向市场化的重要研究课题之一。市场化的前提包括广阔的应用领域,优良的结构性能,良好的可加工性,较低的成本。在能源危机,环境污染严重的当今,给绿色塑料PLA提供了巨大的商机和市场前景。PLA的应用领域已包括包装、纺织、餐饮、轻工、农业等领域。PLA可进行吹膜、挤片、注塑、吸塑、纺丝、挤管、发泡等加工。制品有包装膜、农用地膜、餐具、文具、玩具、服装等。
PLA具有刚性强硬度高,加工容易,性能适中,并可完全生物降解等优点。但韧性差熔体强度低价格偏高一直制约着PLA的进一步应用推广。因此针对PLA的不足进行增韧改性,降低成本就成为该领域的研究重点之一。提高PLA的柔韧性最直接和简便的方法就是共混改性。PLA可以和塑料、橡胶(弹性体)、填料或增塑剂等共混,达到改性的目的。例如专利CA1475530A加入聚丁二酸丁二醇酯(PBS)、专利CN 1250065A加入聚碳酸酯(PC)专利CN1701082加入聚甲醛(POM)等;还有混如增塑剂的专利CN1793228。但是,由于PLA属于脂肪族聚酯,与很多种聚合物的相容性都较差,共混后体系的力学性能会下降。因此,兼顾成本、卫生、环境友好等因素的同时,提高共混组分间的相容性,实现物理力学性能的提高是大家关注的热点。
发明内容
本发明是一种完全生物降解增韧型聚乳酸树脂及制备方法。其是提高PLA韧性的一项技术,将一种丙烯酸酯类共聚物作为增韧剂与PLA进行共混,从而获得一种增韧型聚乳酸树脂及其制备方法。
一种完全生物降解增韧型聚乳酸树脂,其成分及配比如下:
聚乳酸(PLA)基础树脂,加入质量份数为60-95份;
增韧剂为丙烯酸乙酯(EA)-丙烯酸丁酯(BA)-丙烯酸(AA)三元共聚物,加入质量份数为5-40份;所述的增韧剂组成的EA质量分数为40-55%,BA质量分数为40-55%,AA质量分数为5%;
所述的抗氧剂为商品名称B215复合型抗氧剂,其组成为质量配比为1比2的四(β-(3,5-二叔丁基-4-羟基)丙酸)季戊四醇酯与亚磷酸三(2,4,-二叔丁基苯基)酯;其加入的质量份数为:0.5份。
一种完全生物降解增韧型聚乳酸树脂的制备方法的步骤和条件如下:按配比,把聚乳酸(PLA)基础树脂、增韧剂和抗氧剂在60℃烘箱中干燥,然后在橡塑混炼机上密炼,工艺温度180℃,转速40转/分,时间5分钟,得到一种完全生物降解增韧型聚乳酸树脂。
本发明的共混树脂中增韧剂含量为5%时,拉伸强度为41.8-46.7MPa。断裂伸长率为13-97%。Izod冲击强度为6.6-7.9KJ/m2。增韧剂含量为40%时,拉伸强度为7.7-8.9MPa。断裂伸长率为10-25%。Izod冲击强度为7.4-11.9KJ/m2
有益效果:PLA与增韧剂具有较好的相容性,可按任意比例进行混合;增韧剂成本低,混合后可减低成本;原材料无毒无害,产品应用安全卫生;适当调整增韧剂单体配比和增韧剂用量,在较宽的范围内都会得到性能优良的增韧材料。可用于制备薄膜、板材、片材、发泡和注塑成型塑料制品。
具体实施方式
实施例1:将8万分子量的基础树脂PLA95份,增韧剂(EA质量分数为40%、BA质量分数为55%、AA质量分数为5%的三元共聚物)5份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼,测得拉伸强度41.8Mp。伸长率97%。Izod冲击强度7.9KJ/m2
实施例2:将8万分子量的基础树脂PLA90份,增韧剂(EAA质量分数为40%/BAA质量分数为55%/AAA质量分数为5%三元共聚物)10份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度39.4Mp。伸长率122%。Izod冲击强度8.0KJ/m2
实施例3:将8万分子量的基础树脂PLA80份,增韧剂(EAA质量分数为40%/BAA质量分数为55%/AAA质量分数为5%三元共聚物)20份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度26.4Mp。伸长率53%。Izod冲击强度8.4KJ/m2
实施例4:将8万分子量的基础树脂PLA70份,增韧剂(EAA质量分数为40%/BAA质量分数为55%/AAA质量分数为5%三元共聚物)30份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度14.0Mp。伸长率25%。Izod冲击强度9.4KJ/m2
实施例5:将8万分子量的基础树脂PLA60份,增韧剂(EAA质量分数为40%/BAA质量分数为55%/AAA质量分数为5%三元共聚物)40份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度7.66Mp。伸长率25%。Izod冲击强度11.9KJ/m2
实施例6:将8万分子量的基础树脂PLA95份,增韧剂(EAA质量分数为45%/BAA质量分数为50%/AAA质量分数为5%三元共聚物)5份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度46.1Mp。伸长率18%。Izod冲击强度6.9KJ/m2
实施例7:将8万分子量的基础树脂PLA90份,增韧剂(EAA质量分数为45%/BAA质量分数为50%/AAA质量分数为5%三元共聚物)10份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度40.3Mp。伸长率26%。Izod冲击强度7.4KJ/m2
实施例8:将8万分子量的基础树脂PLA质量分数80份,增韧剂(EAA质量分数为45%/BAA质量分数为50%/AAA质量分数为5%三元共聚物)20份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度22.8Mp。伸长率19%。Izod冲击强度9.3KJ/m2
实施例9:将8万分子量的基础树脂PLA70份,增韧剂(EAA质量分数为45%/BAA质量分数为50%/AAA质量分数为5%三元共聚物)30份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度14.8Mp。伸长率12%。Izod冲击强度6.8KJ/m2
实施例10:将8万分子量的基础树脂PLA60份,增韧剂(EAA质量分数为45%/BAA质量分数为50%/AAA质量分数为5%三元共聚物)40份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度8.3Mp。伸长率10%。Izod冲击强度7.4KJ/m2
实施例11:将8万分子量的基础树脂PLA95份,增韧剂(EAA质量分数为50%/BAA质量分数为45%/AAA质量分数为5%三元共聚物)5份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度43.7Mp。伸长率13%。Izod冲击强度6.6KJ/m2
实施例12:将8万分子量的基础树脂PLA份,增韧剂(EAA质量分数为50%/BAA质量分数为45%/AAA质量分数为5%三元共聚物)10份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度38.7Mp。伸长率13%。Izod冲击强度6.7KJ/m2
实施例13:将8万分子量的基础树脂PLA80份,增韧剂(EAA质量分数为50%/BAA质量分数为45%/AAA质量分数为5%三元共聚物)20份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度23.3Mp。伸长率15%。Izod冲击强度7.3KJ/m2
实施例14:将8万分子量的基础树脂PLA70份,增韧剂(EAA质量分数为50%/BAA质量分数为45%/AAA质量分数为5%三元共聚物)30份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度14.2Mp。伸长率16%。Izod冲击强度7.9KJ/m2
实施例15:将8万分子量的基础树脂PLA60份,增韧剂(EAA质量分数为50%/BAA质量分数为45%/AAA质量分数为5%三元共聚物)40份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度8.1Mp。伸长率12%。Izod冲击强度7.9KJ/m2
实施例16:将8万分子量的基础树脂PLA95份,增韧剂(EAA质量分数为55%/BAA质量分数为40%/AAA质量分数为5%三元共聚物)5份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度40.7Mp。伸长率14%。Izod冲击强度7.5KJ/m2
实施例17:将8万分子量的基础树脂PLA90份,增韧剂(EAA质量分数为55%/BAA质量分数为40%/AAA质量分数为5%三元共聚物)10份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度37.0Mp。伸长率27%。Izod冲击强度7.6KJ/m2
实施例18:将8万分子量的基础树脂PLA80份,增韧剂(EAA质量分数为55%/BAA质量分数为40%/AAA质量分数为5%三元共聚物)20份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度25.3Mp。伸长率17%。Izod冲击强度10.1KJ/m2
实施例19:将8万分子量的基础树脂PLA70份,增韧剂(EAA质量分数为55%/BAA质量分数为40%/AAA质量分数为5%三元共聚物)30份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度16.6Mp。伸长率24%。Izod冲击强度8.1KJ/m2
实施例20:将8万分子量的基础树脂PLA60份,增韧剂(EAA质量分数为55%/BAA质量分数为40%/AAA质量分数为5%三元共聚物)40份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度8.9Mp。伸长率23%。Izod冲击强度9.3KJ/m2
实施例21:将3万分子量的基础树脂PLA80份,增韧剂(EAA质量分数为40%/BAA质量分数为55%/AAA质量分数为5%三元共聚物)20份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度18.9Mp。伸长率33%。Izod冲击强度7.7KJ/m2
实施例22:将20万分子量的基础树脂PLA80份,增韧剂(EAA质量分数为40%/BAA质量分数为55%/AAA质量分数为5%三元共聚物)20份,抗氧剂(B215)0.5份加入混炼机中,于180℃,40转/分,5分钟条件下密炼。共混物测得拉伸强度42.3Mp。伸长率68%。Izod冲击强度9.3KJ/m2

Claims (2)

1、一种完全生物降解增韧型聚乳酸树脂,其特征在于,其成分及质量分数配比如下:
聚乳酸基础树脂,加入质量份数为60-95份;
增韧剂为丙烯酸乙酯-丙烯酸丁酯-丙烯酸三元共聚物,加入质量份数为5-40份;所述的增韧剂组成的EA质量分数为40-55%,BA质量分数为40-55%,AA质量分数为5%;
所述的抗氧剂为商品名称B215复合型抗氧剂,其组成为质量配比为1比2的四〔β-(3,5-二叔丁基-4-羟基)丙酸〕季戊四醇酯与亚磷酸三(2,4,-二叔丁基苯基)酯;其加入的质量份数为:0.5份。
2、如权利要求1所述的一种完全生物降解增韧型聚乳酸树脂的制备方法,其特征在于,步骤和条件如下:按配比,把聚乳酸基础树脂、增韧剂和抗氧剂在60℃烘箱中干燥,然后在橡塑混炼机上密炼,工艺温度180℃,转速40转/分,时间5分钟,得到一种完全生物降解增韧型聚乳酸树脂。
CN2008100510649A 2008-08-11 2008-08-11 一种完全生物降解增韧型聚乳酸树脂及制备方法 Active CN101338069B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2008100510649A CN101338069B (zh) 2008-08-11 2008-08-11 一种完全生物降解增韧型聚乳酸树脂及制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2008100510649A CN101338069B (zh) 2008-08-11 2008-08-11 一种完全生物降解增韧型聚乳酸树脂及制备方法

Publications (2)

Publication Number Publication Date
CN101338069A true CN101338069A (zh) 2009-01-07
CN101338069B CN101338069B (zh) 2011-05-04

Family

ID=40212244

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2008100510649A Active CN101338069B (zh) 2008-08-11 2008-08-11 一种完全生物降解增韧型聚乳酸树脂及制备方法

Country Status (1)

Country Link
CN (1) CN101338069B (zh)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090110859A1 (en) * 2007-10-31 2009-04-30 E. I. Du Pont De Nemours And Company Poly(hydroxyalkanoic acid) composition
CN101914274A (zh) * 2010-09-15 2010-12-15 中国科学院长春应用化学研究所 完全生物降解的透明高韧性聚乳酸树脂及其制备方法
CN105733215A (zh) * 2014-12-10 2016-07-06 黑龙江鑫达企业集团有限公司 一种三元无规共聚物增韧聚乳酸复合材料及其制备方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5665824A (en) * 1995-01-31 1997-09-09 Tredegar Industries, Inc. Alkaline and water soluble articles and method of making same
JP4768106B2 (ja) * 2000-07-31 2011-09-07 スリーエム イノベイティブ プロパティズ カンパニー 接着剤組成物及び熱剥離容易な接着構造
WO2006121011A1 (ja) * 2005-05-09 2006-11-16 Kaneka Corporation 生分解性樹脂組成物及びその成形体
CN101168617A (zh) * 2006-10-26 2008-04-30 中国石化仪征化纤股份有限公司 聚乳酸增韧改性的方法

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090110859A1 (en) * 2007-10-31 2009-04-30 E. I. Du Pont De Nemours And Company Poly(hydroxyalkanoic acid) composition
CN101914274A (zh) * 2010-09-15 2010-12-15 中国科学院长春应用化学研究所 完全生物降解的透明高韧性聚乳酸树脂及其制备方法
CN101914274B (zh) * 2010-09-15 2012-07-04 中国科学院长春应用化学研究所 完全生物降解的透明高韧性聚乳酸树脂及其制备方法
CN105733215A (zh) * 2014-12-10 2016-07-06 黑龙江鑫达企业集团有限公司 一种三元无规共聚物增韧聚乳酸复合材料及其制备方法

Also Published As

Publication number Publication date
CN101338069B (zh) 2011-05-04

Similar Documents

Publication Publication Date Title
CN104119647B (zh) 一种高淀粉含量全生物降解组合物及其制备方法
US10941260B2 (en) Plasticized biodegradable polyester film and preparation method thereof
CN108822514B (zh) 一种完全生物降解聚乳酸基吹塑薄膜及其制备方法
CN111040400A (zh) 一种全生物降解片材及其制备方法
CN103013070B (zh) 一种聚乳酸复合材料及其制备方法
CN104072957B (zh) 一种食品级可生物降解聚乳酸基复合材料及其应用
CN108841352B (zh) 一种可生物降解的聚乳酸热熔胶及其制备和应用
CN101333332B (zh) 一种丙烯酸酯类共聚物增韧改性聚乳酸树脂及制备方法
CN103965596B (zh) 一种可生物降解聚乳酸基复合材料及应用
CN102653601A (zh) 可完全生物降解塑料树脂及其薄膜类制品的方法
WO2014032393A1 (zh) 一种全生物降解材料及其制备方法
CN105968757A (zh) 一种全生物降解增韧高强聚乳酸基复合材料及其制备方法
CN104387732A (zh) 一种透明抗撕裂聚乳酸生物降解薄膜及其制备方法
CN101525487A (zh) 一种可环境降解的复合材料及其制备方法
CN102504507A (zh) 一种聚乳酸增韧改性剂及其制备方法
CN108017887A (zh) 一种pla-pbsa吹塑薄膜及其制备方法
WO2023104139A1 (zh) 一种抗冲击能力强的复合高分子材料及其制备方法
CN106674923A (zh) 一种降解可控pbat/pla复合膜及其制备方法
CN105131542B (zh) 一种经丙交酯表面接枝处理的竹粉和聚乳酸共混复合材料及其制备方法与应用
CN101338069B (zh) 一种完全生物降解增韧型聚乳酸树脂及制备方法
TW202407020A (zh) 含多元酸的聚羥基烷酸酯組合物及聚羥基烷酸酯成型體
CN114031914A (zh) 一种生物基吸塑材料及其制备方法
CN113831702B (zh) 可降解塑料餐盒组合物及其制备方法
CN111944291A (zh) 一种聚乳酸树脂组合物及其制备方法
CN1389515A (zh) 可吹塑尼龙复合材料的制备方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
ASS Succession or assignment of patent right

Owner name: CHANGZHOU INSTITUTE OF ENERGY STORAGE MATERIALS +

Free format text: FORMER OWNER: CHANGCHUN INST. OF APPLIED CHEMISTRY, CHINESE ACADEMY OF SCIENCES

Effective date: 20130425

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 130022 CHANGCHUN, JILIN PROVINCE TO: 213000 CHANGZHOU, JIANGSU PROVINCE

TR01 Transfer of patent right

Effective date of registration: 20130425

Address after: Changzhou City, Jiangsu province Hehai road 213000 No. 9

Patentee after: CHANGZHOU INSTITUTE OF ENERGY STORAGE MATERIALS & DEVICES

Address before: 130022 Changchun people's street, Jilin, No. 5625

Patentee before: CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY CHINESE ACADEMY OF SCIENCES

TR01 Transfer of patent right

Effective date of registration: 20180530

Address after: 130022 5625 people's street, Chaoyang District, Changchun, Jilin.

Patentee after: CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY CHINESE ACADEMY OF SCIENCES

Address before: No. 9, river Hai Dong Road, Changzhou, Jiangsu Province

Patentee before: Changzhou Institute of Energy Storage Materials & Devices

TR01 Transfer of patent right
TR01 Transfer of patent right
TR01 Transfer of patent right

Effective date of registration: 20180823

Address after: 130000 Jilin nine Changchun Economic Development Zone, Karen Industrial South District, two road 3.

Patentee after: JILIN KAISHUN NEW MATERIAL Co.,Ltd.

Address before: 130022 5625 people's street, Chaoyang District, Changchun, Jilin.

Patentee before: CHANGCHUN INSTITUTE OF APPLIED CHEMISTRY CHINESE ACADEMY OF SCIENCES

PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: Complete-biodegradable toughening type polylactic resin and preparation method

Effective date of registration: 20200311

Granted publication date: 20110504

Pledgee: China Everbright Bank Limited by Share Ltd. Changchun branch

Pledgor: JILIN KAISHUN NEW MATERIAL Co.,Ltd.

Registration number: Y2020220000004

PE01 Entry into force of the registration of the contract for pledge of patent right
PC01 Cancellation of the registration of the contract for pledge of patent right
PC01 Cancellation of the registration of the contract for pledge of patent right

Date of cancellation: 20210323

Granted publication date: 20110504

Pledgee: China Everbright Bank Limited by Share Ltd. Changchun branch

Pledgor: JILIN KAISHUN NEW MATERIAL Co.,Ltd.

Registration number: Y2020220000004

PE01 Entry into force of the registration of the contract for pledge of patent right
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: A completely biodegradable toughened polylactic acid resin and its preparation method

Effective date of registration: 20210325

Granted publication date: 20110504

Pledgee: China Everbright Bank Limited by Share Ltd. Changchun branch

Pledgor: JILIN KAISHUN NEW MATERIAL Co.,Ltd.

Registration number: Y2021220000029

PC01 Cancellation of the registration of the contract for pledge of patent right
PC01 Cancellation of the registration of the contract for pledge of patent right

Date of cancellation: 20220927

Granted publication date: 20110504

Pledgee: China Everbright Bank Limited by Share Ltd. Changchun branch

Pledgor: JILIN KAISHUN NEW MATERIAL Co.,Ltd.

Registration number: Y2021220000029

PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: A completely biodegradable toughened polylactic acid resin and its preparation method

Effective date of registration: 20231208

Granted publication date: 20110504

Pledgee: China Everbright Bank Limited by Share Ltd. Changchun branch

Pledgor: JILIN KAISHUN NEW MATERIAL Co.,Ltd.

Registration number: Y2023220000139

PE01 Entry into force of the registration of the contract for pledge of patent right