CN104448565A - 一种增强改性聚丙烯材料 - Google Patents

一种增强改性聚丙烯材料 Download PDF

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CN104448565A
CN104448565A CN201410767601.5A CN201410767601A CN104448565A CN 104448565 A CN104448565 A CN 104448565A CN 201410767601 A CN201410767601 A CN 201410767601A CN 104448565 A CN104448565 A CN 104448565A
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parts
polypropylene material
modified polypropylene
polypropylene
reinforcing
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韦良强
孙静
杨庭国
郑红开
明星星
刘小柱
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GUIZHOU KAIKETE MATERIAL CO Ltd
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GUIZHOU KAIKETE MATERIAL CO Ltd
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    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • 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
    • C08K9/00Use of pretreated ingredients
    • C08K9/04Ingredients treated with organic substances
    • 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
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/08Stabilised against heat, light or radiation or oxydation

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

本发明公开了一种增强改性聚丙烯材料,其特征在于:包含以下组分:聚丙烯:60~95份,改性剂:5~20份,相容剂:5~20份,表面处理剂:1~3份。本发明所述的增强改性聚丙烯在强度、模量和热性能方面有明显提高,且所得制品表面光泽度非常好,由于贝壳粉可以吸收分解甲醛、苯、TVOC、氡等有害气体,因此用贝壳粉增强改性得到的聚丙烯材料是一种具有良好外观的新型环保材料,特别在汽车、家装等行业具有良好的市场应用前景。

Description

一种增强改性聚丙烯材料
技术领域
本发明属于高分子材料科学领域,具体涉及一种增强改性聚丙烯材料。
背景技术
聚丙烯为无毒、无臭、无味的乳白色高结晶的聚合物,成本低、性能优异、用途广泛,是目前所有塑料中最轻的品种之一。它对水特别稳定,成型性好,但因收缩率大( 为1% ~ 2.5%),厚壁制品易凹陷,对一些尺寸精度较高零件,还难于达到要求。通过改性剂的添加往往可以优化其性能。对聚丙烯的增韧改性研究目前已经很普遍,如在聚丙烯中加入CaCO3、滑石粉、蒙脱土、木粉等。
发明内容
本发明要解决的技术问题是:提供一种光泽度好的增强改性聚丙烯材料,已解决现有技术的不足。
本发明的技术方案是:一种增强改性聚丙烯材料,包含以下组分:
聚丙烯         60~95份
改性剂         5~20份
相容剂         5~20份
表面处理剂     1~3份。 
所述聚丙烯熔融指数为230℃下9.5g/10min。
所述改性剂为天然贝壳粉。
所述相容剂PP-g-GMA。
所述表面处理剂为钛酸酯偶联剂或硅烷偶联剂。 
本发明的有益效果:本发明所述的增强改性聚丙烯在强度、模量和热性能方面有明显提高,且所得制品表面光泽度非常好,由于贝壳粉可以吸收分解甲醛、苯、TVOC、氡等有害气体,因此用贝壳粉增强改性得到的聚丙烯材料是一种具有良好外观的新型环保材料,特别在汽车、家装等行业具有良好的市场应用前景。
具体实施方式
以下通过具体实施方式的描述对本发明作进一步说明,但这并非是对本发明的限制,本领域技术人员根据本发明的基本思想,可以做出各种修改或改进,但是只要不脱离本发明的基本思想,均在本发明的范围之内。
实施例1:聚丙烯/贝壳粉按重量份数配比100/0、95/5、90/10、85/15、80/20用双螺杆挤出机通过熔融共混法制备增强聚丙烯增强改性材料。实验结果表明:添加量的最佳值为10%,与纯PP相比,拉伸强度提高1.89%,弯曲模量提高19.25%,冲击强度提高60.14%。在弯曲模量和冲击强度的改善上,贝壳粉要优于普通碳酸钙和滑石粉。
实施例2:聚丙烯/PP-g-GMA/贝壳粉按重量份数配比100/0/0、92/3/5、85/5/10、78/7/15、70/10/20用双螺杆挤出机通过熔融共混法制备聚丙烯增强改性材料。实验结果表明:复合材料的流动速率随相容剂用量的增加而逐步下降,拉伸强度和弯曲强度逐步上升,并在相容剂含量为5wt%时达到最佳值。与纯PP相比,复合材料的拉伸强度提高2.09%,弯曲模量提高20.35%。冲击强度提高61.37%。
实施例3:第一步,用2.5wt%的钛酸酯偶联剂对贝壳粉进行处理得到改性贝壳粉。第二步聚丙烯/改性贝壳粉按重量份数配比100/0、95/5、90/10、85/15、80/20用双螺杆挤出机通过熔融共混法制备聚丙烯增强改性材料。与实例1中未进行表面处理的贝壳粉相比,实例3所得到的复合材料拉伸强度、弯曲强度、缺口冲击强度提升4%~6%。
实施例4:按照实施实例3的第一步得到改性贝壳粉,将聚丙烯/PP-g-GMA/改性贝壳粉按重量份数配比100/0/0、92/3/5、85/5/10、78/7/15、70/10/20用双螺杆挤出机通过熔融共混法制备聚丙烯增强改性材料。实验结果表明:按实例3第一步得到改性天然贝壳粉,添加量为10wt%, PP-g-GMA用量为5wt%,采用双螺杆熔融共混挤出得到的聚丙烯/PP-g-GMA/改性贝壳粉复合材料,与纯PP相比,拉伸强度提高5.12%,弯曲模量提高23.05%,冲击强度提高64.12%。

Claims (5)

1.一种增强改性聚丙烯材料,其特征在于:包含以下组分:
聚丙烯         60~95份
改性剂         5~20份
相容剂         5~20份
表面处理剂     1~3份。
2.根据权利要求1所述的一种增强改性聚丙烯材料,其特征在于:所述聚丙烯熔融指数为230℃下9.5g/10min。
3.根据权利要求1所述的一种增强改性聚丙烯材料,其特征在于:所述改性剂为天然贝壳粉。
4.根据权利要求1所述的一种增强改性聚丙烯材料,其特征在于:所述相容剂PP-g-GMA。
5.根据权利要求1所述的一种增强改性聚丙烯材料,其特征在于:所述表面处理剂为钛酸酯偶联剂或硅烷偶联剂。
CN201410767601.5A 2014-12-15 2014-12-15 一种增强改性聚丙烯材料 Pending CN104448565A (zh)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107337854A (zh) * 2017-08-03 2017-11-10 慈溪市赛斯特金属制品有限公司 一种用于生产折叠凳的高流动性聚丙烯及其制备方法
CN108948762A (zh) * 2018-04-25 2018-12-07 曾冬梅 一种聚丙烯阻燃木塑复合板材及制备方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1475520A (zh) * 2002-08-15 2004-02-18 孙建宁 贝壳微粉填料及其用途
CN102070831A (zh) * 2010-12-21 2011-05-25 东华大学 增韧聚丙烯复合材料及其制备方法
CN102227477A (zh) * 2009-09-30 2011-10-26 索尼公司 树脂组合物及发泡成形体

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1475520A (zh) * 2002-08-15 2004-02-18 孙建宁 贝壳微粉填料及其用途
CN102227477A (zh) * 2009-09-30 2011-10-26 索尼公司 树脂组合物及发泡成形体
CN102070831A (zh) * 2010-12-21 2011-05-25 东华大学 增韧聚丙烯复合材料及其制备方法

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107337854A (zh) * 2017-08-03 2017-11-10 慈溪市赛斯特金属制品有限公司 一种用于生产折叠凳的高流动性聚丙烯及其制备方法
CN108948762A (zh) * 2018-04-25 2018-12-07 曾冬梅 一种聚丙烯阻燃木塑复合板材及制备方法

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Application publication date: 20150325