CN107141599A - 一种改性pp发泡增强材料及其制备方法 - Google Patents

一种改性pp发泡增强材料及其制备方法 Download PDF

Info

Publication number
CN107141599A
CN107141599A CN201710474885.2A CN201710474885A CN107141599A CN 107141599 A CN107141599 A CN 107141599A CN 201710474885 A CN201710474885 A CN 201710474885A CN 107141599 A CN107141599 A CN 107141599A
Authority
CN
China
Prior art keywords
modified
areas
foaming
reinforcing material
parts
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
Application number
CN201710474885.2A
Other languages
English (en)
Inventor
陶宇
翁亚楠
朱建
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.)
Changchang Tanrun New Material Co Ltd
Original Assignee
Changchang Tanrun New Material Co Ltd
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 Changchang Tanrun New Material Co Ltd filed Critical Changchang Tanrun New Material Co Ltd
Priority to CN201710474885.2A priority Critical patent/CN107141599A/zh
Publication of CN107141599A publication Critical patent/CN107141599A/zh
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions 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
    • C08L23/10Homopolymers or copolymers of propene
    • C08L23/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/20Compounding polymers with additives, e.g. colouring
    • C08J3/22Compounding polymers with additives, e.g. colouring using masterbatch techniques
    • C08J3/226Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J9/00Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
    • C08J9/04Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
    • C08J9/06Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
    • C08J9/10Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent developing nitrogen, the blowing agent being a compound containing a nitrogen-to-nitrogen bond
    • C08J9/102Azo-compounds
    • C08J9/103Azodicarbonamide
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2203/00Foams characterized by the expanding agent
    • C08J2203/04N2 releasing, ex azodicarbonamide or nitroso compound
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/04Homopolymers or copolymers of ethene
    • C08J2323/08Copolymers of ethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2323/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2323/02Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
    • C08J2323/10Homopolymers or copolymers of propene
    • C08J2323/12Polypropene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/014Additives containing two or more different additives of the same subgroup in C08K
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2203/00Applications
    • C08L2203/14Applications used for foams
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)

Abstract

本发明属于高分子材料改性技术领域,具体涉及一种改性PP发泡增强材料及其制备方法。该改性PP发泡增强材料由改性PP颗粒和发泡母粒组成;其中,改性PP颗粒由PP、无机矿物填充剂、增韧剂、短玻纤、抗氧剂1010、表面活性剂组成;发泡母粒由EVA、滑石粉、发泡剂、助发泡剂、交联剂、助交联剂、抗氧剂1010组成。本发明先对PP进行增强改性,再进行化学发泡,使得制备出来的PP发泡材料既具有低密度,又具备良好的拉伸强度、弯曲强度和冲击强度,可以用于替代目前汽车上不发泡PP制备的门板和仪表台等部件,起到减重、隔热、降噪等目的。

Description

一种改性PP发泡增强材料及其制备方法
技术领域
本发明属于高分子材料改性技术领域,具体涉及一种改性PP发泡增强材料及其制备方法。
背景技术
泡沫塑料具有质轻、隔热、隔音、缓冲、比强度高等优点。因此在包装、工业、农业、交通运输、军事工业、航天工业及日用品等领域得到广泛应用。我国自20世纪90年代以来泡沫塑料的发展也十分迅速,主要品种有聚氨西言聚氨酯(PU)软、硬质泡沫塑料,聚苯乙烯(PS)和聚烯烃发泡材料。然而PU在发泡过程中会产生对人体有害的异氰酸酯残留物,同时无法回收利用;而发泡PS制品废弃物不腐烂、难回收,造成”白色污染”,1991年欧洲共同体制定了强制性的“包装规则”,将发泡PS列入“避免使用”范围。***环保组织已决定到2005年全世界范围内停止生产和使用发泡PS。此时人们釆用性能优异、使于回收利用的发泡聚丙烯(PP)在很多领域来取代其他泡沫材料。
聚丙烯是一种结晶聚合物,其发泡只能在结晶熔点附近进行,超过熔点熔体粘度迅速下降。通用聚丙烯树脂的熔体强度很低,发泡成型非常因难。聚丙烯发泡技术的研究、开发和推广应用,已成为各国关注的焦点。
目前汽车门板模块、仪表台模块多是以改性聚丙烯塑料为原料,材料常见的注塑成型工艺制备而成。这种普通的原料以PP和填充物为主,注塑成型后使得制品质地紧密、密度高、重量大,增加了产品的用料与成本,不利于当前汽车轻量化设计理念,而且制品表面容易出现蠕变、缩痕等缺陷,严重影响了制品的外观与品质。同时由于这种质地紧密的制品不能很好的隔热与隔音,使得在制品上需要另附一层隔热隔音材料,增加成本,工艺复杂。因而发泡PP材料则可以很好的解决这些问题。目前市场上现有的PP发泡材料虽然具有低密度,但是并没有良好的物理力学性能。本发明公开了一种改性PP发泡增强材料及其制备方法,其具有低密度、高强度、耐候、耐老化等特性,可用于包装、汽车、缓冲衬垫、吸声降噪等领域。尤其可以用于替代目前汽车上不发泡PP制备的门板和仪表台等部件,起到减重、隔热、降噪等目的。
发明内容
为了克服现有技术的不足,本发明的目的在于对PP进行增强改性,再进行化学发泡,制备低密度增强PP发泡材料;使得制备出来的PP发泡材料既具有低密度,又具备良好的拉伸强度、弯曲强度和冲击强度,可以用于替代目前汽车上不发泡PP制备的门板和仪表台等部件,起到减重、隔热、降噪等目的。
为了实现上述目的,本发明采用如下技术方案:
一种改性PP发泡增强材料,所述的改性PP发泡增强材料由改性PP颗粒和发泡母粒组成,两者的质量比为100:(4~9)。
具体地,上述的改性PP颗粒各组分按质量份数计为:
PP:50~60份
无机矿物填充剂:30份
增韧剂:5~16份
短玻纤:3~5份
抗氧剂1010:0.2份
表面活性剂:0.2份。
具体地,上述的PP的熔融指数1~3g/10min。
具体地,上述的无机矿物填充剂为滑石粉、蒙脱土和高岭土按质量比例为2:0.5:0.5组成。
具体地,上述的增韧剂为EVA和EPDM按质量比例为1:1组成。
具体地,上述的表面活性剂为硬脂酸。
具体地,上述的发泡母粒各组分按质量份数计为:
EVA:45~60份
滑石粉:20~30份
发泡剂:10~20份
助发泡剂:2~5份
交联剂:0.5份
助交联剂:0.2份
抗氧剂1010;0.3份。
具体地,上述的EVA为VA含量28%,MI为40的E。
具体地,上述的发泡剂为偶氮二甲酰胺;所述助发泡剂为氧化锌;所述交联剂为过氧化苯甲酰;所述助交联剂为二乙烯基苯。
一种改性PP发泡增强材料的制备方法,具体包括如下步骤:
(1)制备改性PP颗粒,按照配比称取原料,利用双螺杆挤出机进行挤出造粒,挤出机各区温度:一区150℃,二区160℃,三区175℃,四区180℃,五区180℃,六区180℃,七区180℃,八区180℃,九区190℃,机头180℃;
(2)制备发泡母粒,按照配比称取原料,利用双螺杆挤出机进行挤出造粒,挤出机各区温度:一区不加温,二区60℃,三区70℃,四区85℃,五区85℃,六区90℃,七区85℃,八区80℃,九区80℃,机头80℃;
(3)按一定质量比例称取步骤(1)制备的改性PP颗粒和步骤(2)制备的发泡母粒,利用注塑机进行注塑成型,注塑机各段温度为175℃~190℃。
本发明具有的有益效果:
(1)本发明通过添加不同类型的改性剂以及不同配比的改性剂,在获得低密度PP发泡材料的同时保证了材料的物理力学性能。增加短玻纤能很好的增强材料,但是短玻纤的加入不利于材料的发泡,为了解决此技术难题本发明使用了增韧剂(EVA/EPDM)来改性材料。通过多种配比研究发现,增韧剂的加入能解决短玻纤不利于发泡的难题。
(2)本发明所述的发泡母粒采用EVA作为基材,不仅有利于低温造粒,还能很好的促进粉料的分散,有利于材料获得更大倍率的发泡。
(3)本发明配方原料易得,成本低廉;制备方法操作简单,工艺条件易控制,运行成本低,生产效率高,制备的产品性能好,可以用于替代目前汽车上不发泡PP制备的门板和仪表台等部件,起到减重、隔热、降噪等目的。
具体实施方式
现在结合实施例对本发明作进一步详细的说明。
实施例1
一种改性PP发泡增强材料由改性PP颗粒和发泡母粒组成,两者的质量比为100:4。
其中,所述的改性PP颗粒各组分按质量份数计为:
PP:50份
无机矿物填充剂:30份
增韧剂:16份
短玻纤:5份
抗氧剂1010:0.2份
硬脂酸:0.2份。
其中,所述的发泡母粒各组分按质量份数计为:
EVA:45份
滑石粉:30份
偶氮二甲酰胺(AC):20份
氧化锌:5份
过氧化苯甲酰(BPO):0.5份
二乙烯基苯:0.2份
抗氧剂1010;0.3份。
所述的PP的熔融指数1g/10min。
所述的无机矿物填充剂为滑石粉、蒙脱土和高岭土按质量比例为2:0.5:0.5组成。
所述的增韧剂为EVA和EPDM按质量比例为1:1组成。
所述的EVA为VA含量28%,MI为40的聚醋酸乙烯酯。
进一步,上述所述的一种改性PP发泡增强材料的制备方法,具体包括如下步骤:
(1)制备改性PP颗粒,按照配比称取原料,利用双螺杆挤出机进行挤出造粒,挤出机各区温度:一区150℃,二区160℃,三区175℃,四区180℃,五区180℃,六区180℃,七区180℃,八区180℃,九区190℃,机头180℃;
(2)制备发泡母粒,按照配比称取原料,利用双螺杆挤出机进行挤出造粒,挤出机各区温度:一区不加温,二区60℃,三区70℃,四区85℃,五区85℃,六区90℃,七区85℃,八区80℃,九区80℃,机头80℃;
(3)按一定质量比例称取步骤(1)制备的改性PP颗粒和步骤(2)制备的发泡母粒,利用注塑机进行注塑成型,注塑机各段温度为175℃~190℃。
实施例2-4、对比例1-7与实施例1基本相同,不同之处在于表1。
表1
使用螺杆挤出机根据以上实施例分别对改性PP和发泡母粒进行造粒。
改性PP颗粒和发泡母粒配比:
按照以上实施例,称取改性PP颗粒与发泡母粒,混合均匀,使用注塑机注射成型,测试性能如表2。
表2
以上述依据本发明的理想实施例为启示,通过上述的说明内容,相关工作人员完全可以在不偏离本项发明技术思想的范围内,进行多样的变更以及修改。本项发明的技术性范围并不局限于说明书上的内容,必须要根据权利要求范围来确定其技术性范围。

Claims (10)

1.一种改性PP发泡增强材料,其特征在于:所述的改性PP发泡增强材料由改性PP颗粒和发泡母粒组成,两者的质量比为100:(4~9)。
2.如权利要求1所述的一种改性PP发泡增强材料,其特征在于:所述的改性PP颗粒各组分按质量份数计为:
PP:50~60份
无机矿物填充剂:30份
增韧剂:5~16份
短玻纤:3~5份
抗氧剂1010:0.2份
表面活性剂:0.2份。
3.如权利要求2所述的一种改性PP发泡增强材料,其特征在于:所述的PP的熔融指数1~3g/10min。
4.如权利要求2所述的一种改性PP发泡增强材料,其特征在于:所述的无机矿物填充剂为滑石粉、蒙脱土和高岭土按质量比例为2:0.5:0.5组成。
5.如权利要求2所述的一种改性PP发泡增强材料,其特征在于:所述的增韧剂为EVA和EPDM按质量比例为1:1组成。
6.如权利要求2所述的一种改性PP发泡增强材料,其特征在于:所述的表面活性剂为硬脂酸。
7.如权利要求1所述的一种改性PP发泡增强材料,其特征在于:所述的发泡母粒各组分按质量份数计为:
EVA:45~60份
滑石粉:20~30份
发泡剂:10~20份
助发泡剂:2~5份
交联剂:0.5份
助交联剂:0.2份
抗氧剂1010;0.3份。
8.如权利要求7所述的一种改性PP发泡增强材料,其特征在于:所述的EVA为VA含量28%,MI为40的E。
9.如权利要求7所述的一种改性PP发泡增强材料,其特征在于:所述的发泡剂为偶氮二甲酰胺;所述助发泡剂为氧化锌;所述交联剂为过氧化苯甲酰;所述助交联剂为二乙烯基苯。
10.一种如权利要求1-9任一项所述的改性PP发泡增强材料的制备方法,其特征在于:具体包括如下步骤:
(1)制备改性PP颗粒,按照配比称取原料,利用双螺杆挤出机进行挤出造粒,挤出机各区温度:一区150℃,二区160℃,三区175℃,四区180℃,五区180℃,六区180℃,七区180℃,八区180℃,九区190℃,机头180℃;
(2)制备发泡母粒,按照配比称取原料,利用双螺杆挤出机进行挤出造粒,挤出机各区温度:一区不加温,二区60℃,三区70℃,四区85℃,五区85℃,六区90℃,七区85℃,八区80℃,九区80℃,机头80℃;
(3)按一定质量比例称取步骤(1)制备的改性PP颗粒和步骤(2)制备的发泡母粒,利用注塑机进行注塑成型,注塑机各段温度为175℃~190℃。
CN201710474885.2A 2017-06-21 2017-06-21 一种改性pp发泡增强材料及其制备方法 Pending CN107141599A (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710474885.2A CN107141599A (zh) 2017-06-21 2017-06-21 一种改性pp发泡增强材料及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710474885.2A CN107141599A (zh) 2017-06-21 2017-06-21 一种改性pp发泡增强材料及其制备方法

Publications (1)

Publication Number Publication Date
CN107141599A true CN107141599A (zh) 2017-09-08

Family

ID=59782744

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710474885.2A Pending CN107141599A (zh) 2017-06-21 2017-06-21 一种改性pp发泡增强材料及其制备方法

Country Status (1)

Country Link
CN (1) CN107141599A (zh)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109824975A (zh) * 2019-01-04 2019-05-31 江苏理工学院 一种pp发泡材料及其制备方法
CN110271165A (zh) * 2019-08-01 2019-09-24 杭州高兴工程塑料有限公司 一种用于改性pp的双螺杆挤出机

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106810766A (zh) * 2017-01-16 2017-06-09 常州神鹰碳塑复合材料有限公司 一种pp改性发泡增强材料

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106810766A (zh) * 2017-01-16 2017-06-09 常州神鹰碳塑复合材料有限公司 一种pp改性发泡增强材料

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109824975A (zh) * 2019-01-04 2019-05-31 江苏理工学院 一种pp发泡材料及其制备方法
CN110271165A (zh) * 2019-08-01 2019-09-24 杭州高兴工程塑料有限公司 一种用于改性pp的双螺杆挤出机

Similar Documents

Publication Publication Date Title
CN103254653B (zh) 玄武岩纤维增强木塑复合材料及其制备方法
CN110294923B (zh) 微发泡全生物降解聚合物片材及其制备方法
CN108164914B (zh) 一种微发泡注塑abs复合材料及其制备方法
CN102702560B (zh) 一种聚丙烯发泡材料的复合发泡制造方法
CN103102585A (zh) 木塑挤出发泡专用料及其制备方法
CN107698861B (zh) 电子辐照交联发泡聚丙烯片材的制备方法
CN107141599A (zh) 一种改性pp发泡增强材料及其制备方法
CN109776953A (zh) 一种低介电常数挤出级聚丙烯增强材料及制备方法与挤出成型工艺
CN106432887B (zh) 一种聚烯烃发泡母粒的组成及制备方法和用途
CN103396675A (zh) 用于注塑级微发泡木塑复合材料的原材料的处理方法
CN106479143A (zh) 一种凹凸棒土/聚乳酸纳米复合材料及其制备方法
CN105602114A (zh) 一种聚丙烯发泡复合板及其制作方法
CN106810766A (zh) 一种pp改性发泡增强材料
CN104072880B (zh) 一种tpo发泡微球的制备方法以及应用
CN103009761A (zh) 一种高收缩率聚烯烃热收缩薄膜及其制造方法
CN110549707B (zh) 一种发泡聚丙烯复合片材及其制备方法
CN107858008A (zh) 一种竹塑纳米复合材料的制备方法
CN104017348A (zh) 一种聚碳酸亚丙酯改性复合材料及其制备方法
CN107141569A (zh) 一种高硬度pvc光面木塑板及其制备方法
CN103224668A (zh) 一种聚丙烯基竹塑发泡复合材料的制备方法
CN113292760B (zh) 交联间规聚丙烯泡沫及其制备方法和应用
CN102443237A (zh) 一种环保型高发泡用高熔体强度聚丙烯材料的制备方法
CN104817772A (zh) 一种废旧发泡聚苯乙烯回收利用的新方法
CN112430384B (zh) 一种生物基降解再生能源聚合塑料粒子的制备工艺
CN105837900A (zh) 一种高强度环保中空板专用料的制备方法

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20170908

WD01 Invention patent application deemed withdrawn after publication