CN106750942A - 一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法 - Google Patents

一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法 Download PDF

Info

Publication number
CN106750942A
CN106750942A CN201611195962.2A CN201611195962A CN106750942A CN 106750942 A CN106750942 A CN 106750942A CN 201611195962 A CN201611195962 A CN 201611195962A CN 106750942 A CN106750942 A CN 106750942A
Authority
CN
China
Prior art keywords
hydridization
silica aerogel
preparation
aluminium
polypropylene
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
CN201611195962.2A
Other languages
English (en)
Inventor
唐晋
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.)
Fuyang Three Packing Materials Co Ltd
Original Assignee
Fuyang Three Packing Materials 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 Fuyang Three Packing Materials Co Ltd filed Critical Fuyang Three Packing Materials Co Ltd
Priority to CN201611195962.2A priority Critical patent/CN106750942A/zh
Publication of CN106750942A publication Critical patent/CN106750942A/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
    • 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
    • C08J2323/10Homopolymers or copolymers of propene
    • C08J2323/12Polypropene
    • 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
    • C08J2451/00Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers
    • C08J2451/06Characterised by the use of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/02Flame or fire retardant/resistant
    • 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
    • C08L2205/035Polymer mixtures characterised by other features containing three or more polymers in a blend containing four 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)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

本发明公开了一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板,该发泡材料具有良好的亲和性和柔韧性,对不同极性的填料的相容性更佳,有效改善了传统聚丙烯发泡的缺陷;加入的杂化铝硅气凝胶是一种具有独特的纳米多孔结构的化合物,兼具阻燃和增强效果,其填充于树脂体系中后可与熔体良好结合吸附,达到均匀稳定的增强改性效果,可显著的提高熔体的难燃系数,减少传统阻燃剂的用量;本发明制备的聚丙烯发泡材料强度高、抗冲击韧性强,环保阻燃,经济耐用,极具应用前景。

Description

一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法
技术领域
本发明涉及高分子阻燃发泡材料技术领域,尤其涉及一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法。
背景技术
高分子发泡材料是一种由聚合物和包含气体泡孔组成的特殊材料,与普通聚合物材料相比具有密度低、比强度高、隔音减震、隔热等优势,在商品包装、衬垫等领域被广泛应用。目前市场上常见的用作包装的高分子发泡材料有聚乙烯发泡材料、聚丙烯发泡材料、聚苯乙烯发泡材料、EVA发泡材料等,其中聚丙烯发泡材料是一种环保型发泡材料,性价比优、可多次回收利用,应用前景较好。目前聚丙烯发泡的难点在于加工温度超过熔点后,PP的熔体强度极速下降,熔体包裹气体的能力下降,导致泡孔塌陷,难以制得合格的发泡制品。除此之外,有机发泡材料的易燃性也是使用者不得不注意的问题,对发泡材料进行阻燃改性具有重要的实际应用意义。
为了提高聚丙烯发泡材料的阻燃性,许多研究者做了大量的工作,最常见的方法为添加阻燃剂来提高材料的阻燃效果,也有将多种材料协同作用来提高聚丙烯的阻燃性,其中膨胀型阻燃剂(IFR)具有阻燃效率高、低烟、低毒等优点,但是其与PP相容性差、使用量大、易吸潮,通常会导致聚丙烯的力学性能大大降低,发泡过程中也将对熔体产生不良影响,发泡效果差,从而影响使用性能。《纳米二氧化硅增强增韧膨胀型阻燃共聚聚丙烯性能的研究》一文通过添加纳米二氧化硅的方法来改善膨胀型阻燃聚丙烯的力学性能,纳米二氧化硅的添加在一定程度了改善了阻燃剂对聚丙烯产生的不良影响,但是有研究表明,纳米二氧化硅的用量对聚丙烯发泡过程有至关重要的影响,用量过大时纳米粒子容易团聚而导致发泡率低,但是过低的纳米材料不能弥补阻燃剂对体系的不良影响,最终出现了产品要么发泡效果好,阻燃性差,要么阻燃效果较好,但是发泡效果差的困境。
气凝胶特有的纳米多孔网络结构使其在光学、热学、电学、声学等等领域表现出许多独特的性质,以SiO2气凝胶为代表的气凝胶产品在多个领域均显示出巨大的应用前景,其具有隔热、保温、阻燃等多种效果,若将其应用于高分子发泡材料中,将对材料的发泡过程有良好的促进作用,但是SiO2气凝胶力学性能不佳,脆性较大,需要对其做进一步的改性处理。
发明内容
本发明为了弥补已有技术的缺陷,提供一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法,利用气凝胶独特的性能和结构特点,对树脂体系进行改性处理,以期获得高阻燃、高强度的发泡聚丙烯材料。
本发明是通过以下技术方案实现的:
一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板,该发泡材料由以下重量份的原料制得:聚丙烯65-72、马来酸酐接枝聚丙烯5-6、聚烯烃弹性体10-12.5、纳米全硫化橡胶粒子3-5、发泡剂AC 1-3、抗氧剂0.1-0.2、有机磷系阻燃剂0.5-0.8、季戊四醇5-8、异丙醇铝0.3-0.5、异丙醇1-2、聚乙烯吡咯烷酮0.05-0.08、硅烷偶联剂0.1-0.2、正硅酸乙酯3-5、去离子水100-150、浓硝酸0.04-0.06、0.01mol/L的草酸水溶液10-15、无水乙醇5-8。
所述的有机磷系阻燃剂为磷酸甲苯二苯酯、磷酸三苯酯、磷酸三异丙基苯酯、双酚A-双(二苯基磷酸酯)、磷酸三甲苯酯、磷酸三(2-氯丙基)酯、环状磷酸酯中的一种或多种的混合。
所述的一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板的制备方法包括以下步骤:
(1)先将聚乙烯吡咯烷酮、去离子水混合,加热至90-95℃,搅拌混合均匀后溶液恒温备用;
(2)将异丙醇铝研细后投入异丙醇中,超声分散处理30-40min,随后将所得溶液在搅拌状态下滴入步骤(1)制备的溶液中,滴加时间控制在2-3h,滴加完毕后体系恒温继续搅拌反应2-3h,最后加入硝酸,继续恒温搅拌3-5h,得铝溶胶备用;
(3)将正硅酸乙酯投入无水乙醇中,搅拌混合均匀后加入草酸水溶液,在50-60℃水浴条件下搅拌反应3-5h,制成硅溶胶,随后加入步骤(2)制备的铝溶胶,搅拌混合均匀后体系在50-60℃烘箱中凝胶24-38h,随后取出凝胶,依次投入去离子水、无水乙醇中清洗置换2-3次,随后采用超临界干燥技术对凝胶进行处理,在45-50℃,10-15MPa的条件下干燥2-3h,得杂化铝硅气凝胶备用;
(4)将步骤(3)制备的杂化铝硅气凝胶与硅烷偶联剂混合后球磨处理30-50min,过100目筛,将所得物料与其它剩余原料一起投入高速混合机中混合均匀,随后将混合好的物料送至挤出机中,物料在螺杆料筒中经加热熔融、混炼、挤压、发泡,然后经挤出机挤出、模具定型后即得产品,其中料筒温度为195-205℃,螺杆转速为40-50转/分钟,模具温度为175-182℃,压力为1-5MPa。
本发明制备的聚丙烯发泡材料采用聚丙烯、马来酸酐接枝聚丙烯、聚烯烃弹性体复合作为树脂基料,并加入纳米全硫化橡胶粒子作为增韧剂,这种树脂基料具有良好的力学性能,更易发泡,发泡后产品的韧性更佳,并具有良好的亲和性,对不同极性的填料的相容性更佳,有效改善了传统聚丙烯发泡的缺陷;加入的杂化铝硅气凝胶是一种具有独特的纳米多孔结构的化合物,兼具阻燃和增强效果,其填充于树脂体系中后可与熔体良好结合吸附,达到均匀稳定的增强改性效果,可显著的提高熔体的难燃系数,减少传统阻燃剂的用量;本发明制备的聚丙烯发泡材料强度高、抗冲击韧性强,环保阻燃,经济耐用,极具应用前景。
具体实施方式
一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板,该发泡材料由以下重量份的原料制得:聚丙烯65、马来酸酐接枝聚丙烯5、聚烯烃弹性体10、纳米全硫化橡胶粒子3、发泡剂AC1、抗氧剂0.1、磷酸甲苯二苯酯0.5、季戊四醇5、异丙醇铝0.3、异丙醇1、聚乙烯吡咯烷酮0.05、硅烷偶联剂0.1、正硅酸乙酯3、去离子水100、浓硝酸0.04、0.01mol/L的草酸水溶液10、无水乙醇5。
该实施例阻燃聚丙烯发泡板的制备方法包括以下步骤:
(1)先将聚乙烯吡咯烷酮、去离子水混合,加热至90℃,搅拌混合均匀后溶液恒温备用;
(2)将异丙醇铝研细后投入异丙醇中,超声分散处理30min,随后将所得溶液在搅拌状态下滴入步骤(1)制备的溶液中,滴加时间控制在2h,滴加完毕后体系恒温继续搅拌反应2h,最后加入硝酸,继续恒温搅拌3h,得铝溶胶备用;
(3)将正硅酸乙酯投入无水乙醇中,搅拌混合均匀后加入草酸水溶液,在50℃水浴条件下搅拌反应3h,制成硅溶胶,随后加入步骤(2)制备的铝溶胶,搅拌混合均匀后体系在50℃烘箱中凝胶24h,随后取出凝胶,依次投入去离子水、无水乙醇中清洗置换2次,随后采用超临界干燥技术对凝胶进行处理,在45℃,10MPa的条件下干燥2h,得杂化铝硅气凝胶备用;
(4)将步骤(3)制备的杂化铝硅气凝胶与硅烷偶联剂混合后球磨处理30min,过100目筛,将所得物料与其它剩余原料一起投入高速混合机中混合均匀,随后将混合好的物料送至挤出机中,物料在螺杆料筒中经加热熔融、混炼、挤压、发泡,然后经挤出机挤出、模具定型后即得产品,其中料筒温度为195℃,螺杆转速为50转/分钟,模具温度为175℃,压力为1MPa。
将制得发泡板取标准试样,并遵循相关标准进行性能测试,测试结果为:
泡孔密度:0.15×107个/cm3
熔体质量流动速率:0.72g/10min ;
shore A硬度:70.5;
拉伸强度:19.2MPa;
延伸率:482%;
UL94阻燃等级:V0;
极限氧指数:28.8。

Claims (3)

1.一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板,其特征在于,该发泡材料由以下重量份的原料制得:聚丙烯65-72、马来酸酐接枝聚丙烯5-6、聚烯烃弹性体10-12.5、纳米全硫化橡胶粒子3-5、发泡剂AC 1-3、抗氧剂0.1-0.2、有机磷系阻燃剂0.5-0.8、季戊四醇5-8、异丙醇铝0.3-0.5、异丙醇1-2、聚乙烯吡咯烷酮0.05-0.08、硅烷偶联剂0.1-0.2、正硅酸乙酯3-5、去离子水100-150、浓硝酸0.04-0.06、0.01mol/L的草酸水溶液10-15、无水乙醇5-8。
2.如权利要求1所述的一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板,其特征在于,所述的有机磷系阻燃剂为磷酸甲苯二苯酯、磷酸三苯酯、磷酸三异丙基苯酯、双酚A-双(二苯基磷酸酯)、磷酸三甲苯酯、磷酸三(2-氯丙基)酯、环状磷酸酯中的一种或多种的混合。
3.如权利要求1所述的一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板的制备方法,其特征在于,所述的制备方法包括以下步骤:
(1)先将聚乙烯吡咯烷酮、去离子水混合,加热至90-95℃,搅拌混合均匀后溶液恒温备用;
(2)将异丙醇铝研细后投入异丙醇中,超声分散处理30-40min,随后将所得溶液在搅拌状态下滴入步骤(1)制备的溶液中,滴加时间控制在2-3h,滴加完毕后体系恒温继续搅拌反应2-3h,最后加入硝酸,继续恒温搅拌3-5h,得铝溶胶备用;
(3)将正硅酸乙酯投入无水乙醇中,搅拌混合均匀后加入草酸水溶液,在50-60℃水浴条件下搅拌反应3-5h,制成硅溶胶,随后加入步骤(2)制备的铝溶胶,搅拌混合均匀后体系在50-60℃烘箱中凝胶24-38h,随后取出凝胶,依次投入去离子水、无水乙醇中清洗置换2-3次,随后采用超临界干燥技术对凝胶进行处理,在45-50℃,10-15MPa的条件下干燥2-3h,得杂化铝硅气凝胶备用;
(4)将步骤(3)制备的杂化铝硅气凝胶与硅烷偶联剂混合后球磨处理30-50min,过100目筛,将所得物料与其它剩余原料一起投入高速混合机中混合均匀,随后将混合好的物料送至挤出机中,物料在螺杆料筒中经加热熔融、混炼、挤压、发泡,然后经挤出机挤出、模具定型后即得产品,其中料筒温度为195-205℃,螺杆转速为40-50转/分钟,模具温度为175-182℃,压力为1-5MPa。
CN201611195962.2A 2016-12-22 2016-12-22 一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法 Pending CN106750942A (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611195962.2A CN106750942A (zh) 2016-12-22 2016-12-22 一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611195962.2A CN106750942A (zh) 2016-12-22 2016-12-22 一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法

Publications (1)

Publication Number Publication Date
CN106750942A true CN106750942A (zh) 2017-05-31

Family

ID=58899278

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201611195962.2A Pending CN106750942A (zh) 2016-12-22 2016-12-22 一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法

Country Status (1)

Country Link
CN (1) CN106750942A (zh)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112724518A (zh) * 2020-12-28 2021-04-30 鑫龙立新材料扬州有限公司 一种环保胶管及其制备方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102604202A (zh) * 2011-12-26 2012-07-25 上海金发科技发展有限公司 一种玻纤增强无卤阻燃聚丙烯复合材料及其制备方法
CN104327549A (zh) * 2014-10-31 2015-02-04 西南交通大学 硅铝水凝胶双层包覆改性聚磷酸铵及其在阻燃聚丙烯中的应用

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102604202A (zh) * 2011-12-26 2012-07-25 上海金发科技发展有限公司 一种玻纤增强无卤阻燃聚丙烯复合材料及其制备方法
CN104327549A (zh) * 2014-10-31 2015-02-04 西南交通大学 硅铝水凝胶双层包覆改性聚磷酸铵及其在阻燃聚丙烯中的应用

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112724518A (zh) * 2020-12-28 2021-04-30 鑫龙立新材料扬州有限公司 一种环保胶管及其制备方法
CN112724518B (zh) * 2020-12-28 2022-03-15 鑫龙立新材料扬州有限公司 一种环保胶管及其制备方法

Similar Documents

Publication Publication Date Title
CN106832571A (zh) 一种杂化纤维素硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法
CN101717514B (zh) 一种改性酚醛树脂及其泡沫材料和制备方法
CN111253664B (zh) 一种气凝胶发泡聚乙烯棉复合材料的制备方法
CN111019308B (zh) 一种隔热型pla复合塑料瓶及其制备方法
CN103396675B (zh) 用于注塑级微发泡木塑复合材料的原材料的处理方法
CN103553487B (zh) 一种复合轻质保温材料及其制备方法
CN105086273A (zh) 一种抑菌防霉pvc木塑复合材料
CN102898104A (zh) 一种用于外墙外保温系统复合发泡水泥板及其生产方法
CN108659263A (zh) 一种改性碳酸钙及其在pvc木塑复合板的应用
CN106393901A (zh) 一种吸音保温装饰用壁纸
CN106750940A (zh) 一种杂化三聚氰胺‑甲醛硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法
CN106117741A (zh) 一种聚乙烯复合泡沫材料及其制备方法
CN106750942A (zh) 一种杂化铝硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法
CN107057180A (zh) 一种杂化稀土硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法
CN106750941A (zh) 一种杂化芳纶纤维硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法
CN105885232A (zh) 一种汽车保险杠用高性能聚丙烯
CN108948465A (zh) 一种高强度绝热管道及其制备方法
CN106810761A (zh) 一种杂化聚四氟乙烯硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法
CN107235693A (zh) 一种保温材料的制备工艺
CN107163551A (zh) 一种具有净化空气功能的纳米材料及其制备方法
CN113061335A (zh) 一种环保阻燃建筑保温材料及其制备方法
CN108610092A (zh) 一种高强度建筑保温材料及其制备方法
CN115304836A (zh) 一种低硫橡塑海绵制品及其制备方法
CN106832570A (zh) 一种杂化纳米羟基锡酸锌硅气凝胶改性的阻燃聚丙烯发泡板及其制备方法
CN109233126A (zh) 一种聚苯乙烯阻燃发泡板材及制备方法

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
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20170531