CN107522962A - 一种阻燃保温板及其制备方法 - Google Patents

一种阻燃保温板及其制备方法 Download PDF

Info

Publication number
CN107522962A
CN107522962A CN201710906439.4A CN201710906439A CN107522962A CN 107522962 A CN107522962 A CN 107522962A CN 201710906439 A CN201710906439 A CN 201710906439A CN 107522962 A CN107522962 A CN 107522962A
Authority
CN
China
Prior art keywords
fire
heat insulation
insulation plate
retardant heat
preparation
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
CN201710906439.4A
Other languages
English (en)
Other versions
CN107522962B (zh
Inventor
魏亮
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.)
Anhui Longda Building Material Technology Co ltd
Original Assignee
Zhejiang Diheng Industrial 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 Zhejiang Diheng Industrial Co Ltd filed Critical Zhejiang Diheng Industrial Co Ltd
Priority to CN201810285609.6A priority Critical patent/CN108822465B/zh
Priority to CN201710906439.4A priority patent/CN107522962B/zh
Publication of CN107522962A publication Critical patent/CN107522962A/zh
Application granted granted Critical
Publication of CN107522962B publication Critical patent/CN107522962B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/06Polystyrene
    • 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
    • C08J9/0014Use of organic additives
    • C08J9/0028Use of organic additives containing nitrogen
    • 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
    • C08J9/0061Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof characterized by the use of several polymeric components
    • 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
    • C08J9/009Use of pretreated compounding ingredients
    • 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
    • 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
    • C08J9/104Hydrazines; Hydrazides; Semicarbazides; Semicarbazones; Hydrazones; Derivatives thereof
    • 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
    • C08J9/107Nitroso compounds
    • 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
    • C08J2325/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
    • C08J2325/02Homopolymers or copolymers of hydrocarbons
    • C08J2325/04Homopolymers or copolymers of styrene
    • C08J2325/06Polystyrene
    • 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
    • C08J2351/00Characterised 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
    • C08J2351/04Characterised 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 rubbers
    • 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
    • C08J2419/00Characterised by the use of rubbers not provided for in groups C08J2407/00 - C08J2417/00
    • C08J2419/02Latex
    • 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
    • C08K2201/002Physical properties
    • C08K2201/004Additives being defined by their length
    • 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
    • C08K2201/011Nanostructured additives
    • 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

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)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

本发明公开了一种阻燃保温板及其制备方法,所述阻燃保温板是以三聚氰胺氰尿酸盐溶液、纳米碳管、高抗冲性聚苯乙烯、碳纤维、发泡剂、浸渍液和硅烷偶联剂为原料制备而成的;其制备方法是将纳米碳管分散于乙醇,并加入硅烷偶联剂搅拌;然后与高抗冲性聚苯乙烯共混,得到改性聚苯乙烯;将改性聚苯乙烯加热后加入发泡剂,经发泡、熟化后得到发泡聚苯乙烯;将碳纤维剪短,在酸性溶液中电解进行阳极表面氧化处理后,置于三聚氰胺氰尿酸盐溶液中浸泡,然后与浸渍液、改性聚苯乙烯混合,成型。本发明阻燃保温板的阻燃性能好、物理机械性能好,且制备工艺简单。

Description

一种阻燃保温板及其制备方法
技术领域
本发明属于建筑材料技术领域,涉及一种保温板,特别是涉及一种阻燃保温板及其制备方法。
背景技术
随着建筑行业的快速发展,保温板已在建筑材料中广泛使用,目前,市场中常用的保温板有硬质聚氨酯发泡板(PU)、酚醛泡沫板(PF)、聚苯乙烯发泡保温板等。聚苯乙烯发泡保温板由于其优异的防腐蚀性、良好的隔热保温性能和抗压抗冲击性能,成为诸多建筑厂商的首选材料。
聚苯乙烯发泡保温板一般分为模塑聚苯乙烯保温板(EPS)和挤塑聚苯乙烯保温板(XPS),与前者相比,做为硬质发泡保温材料的新一代升级,他简化了EPS的生产工艺,提升了材料的各项使用性能和寿命,被广泛应用于墙体保温、低温储藏以及路面防潮等。
然而,对于发泡聚苯乙烯这一类保温材料而言,易燃是这类材料的致密缺点,当发生火灾时候,易燃的外保温材料会燃烧并放出浓烟火灾有害气体,使得处于火灾的人们窒息造成巨大的财产损失和人员伤亡,目前研究中对聚苯乙烯的阻燃改性研究已经做了很多工作,但是改性后的聚苯乙烯发泡材料的物理机械性能往往较低,或者阻燃效果不佳,其应用范围仍然受到较大的制约。
发明内容
为了克服现有技术中保温板所存在的缺陷,本发明公开了一种阻燃保温板及其制备方法,旨在提供一种阻燃性能好、物理机械性能好,制备工艺简单的阻燃保温板。
为达到以上目的,本发明采用的技术方案为:
一种阻燃保温板,是以如下重量份的组分为原料制备而成的:
优选地,所述浸渍液为RFL浸渍液,其中,RFL浸渍液是丁苯吡胶乳、间苯二酚与甲醛水溶液的混合液,用于增强橡胶复合材料与纤维之间界面的相互作用,从而提高粘合强度。
较佳地,所述发泡剂为偶氮二甲酰胺、二亚硝基五次甲基四胺、对甲苯酰胺肼中的一种或多种。
优选地,所述硅烷偶联剂为硅烷偶联剂KH550、硅烷偶联剂KH-560、硅烷偶联剂Si69中的一种或多种。
作为一种优选实施方式,所述碳纤维的长度为1-5mm。
本发明还公开了上述阻燃保温板的一种优选制备方法,该方法是通过如下步骤实现的:
(1)将纳米碳管分散于乙醇中,然后加入硅烷偶联剂在55-65℃下搅拌2-4h;
(2)将经过步骤(1)处理的碳纳米管与高抗冲性聚苯乙烯在80-150℃、30-40r/min条件下共混10-15min,得到改性聚苯乙烯;
(3)将改性聚苯乙烯用饱和蒸汽加热后加入发泡剂,使发泡剂在聚苯乙烯基体中缓慢分散,发泡4-6min后,熟化8-10h,得到发泡聚苯乙烯;
(4)将碳纤维剪切至1-5mm长的短碳纤维,然后浸到酸性溶液中,在电解槽内进行阳极表面氧化处理,处理完成后取出烘干;
(5)将经过步骤(4)处理得到的短碳纤维在三聚氰胺氰尿酸盐溶液中浸泡8-12h后,取出烘干;
(6)将步骤(5)所得物质与浸渍液一同加入到步骤(2)得到的改性聚苯乙烯中混合均匀,然后通过模具成型,切割成所需规格的阻燃保温板。
作为一种优选实施方式,步骤(4)中的酸性溶液为硝酸或酸性重铬酸钾或次氯酸钠与硫酸的混合液。
作为一种优选实施方式,步骤(4)中的处理电压为4.5-5.0V,处理时间为5-15min;较佳地,步骤(4)中的处理电压为4.8V,处理时间为10min。
较佳地,步骤(6)中模具成型后,经过6-10天的养护后,再进行切割。
本发明与现有技术相比,具有如下优点和有益效果:
(1)通过纳米碳管在HIPS中构建交叉网络结构,很大程度上提高了材料的物理机械性能,有效地提高了材料的抗拉和抗弯强度,并且在一定程度中起到了阻燃的效果;
(2)经过电解处理的短纤维表面有较多的突起,与HIPS可以更加牢靠的结合在一起,进一步提高材料的抗拉性能,并且通过MCA的接枝改性,将阻燃剂均匀分散在基体中,避免由于阻燃剂与HIPS普通共混造成的材料性能下降;
(3)由于浸渍液的存在,尤其是RFL浸渍液,缩小了短纤与EPS大颗粒之间的空隙,提高了两者的相容性。
具体实施方式
以下描述用于揭露本发明以使本领域技术人员能够实现本发明。以下描述中的优选实施例只作为举例,本领域技术人员可以想到其他显而易见的变型。
表1组分中所用的原料规格及来源如下:
原料 规格 来源
三聚氰胺氰尿酸盐 - 北京伊诺凯有限公司
纳米碳管 - 时代纳米
高抗冲性聚苯乙烯 - 西格玛试剂
发泡剂 工厂级 广州市天河区鑫沐化工
碳纤维 - 北京伊诺凯有限公司
硅烷偶联剂 分析纯 西格玛试剂
RFL浸渍液 工厂级 广州市天河区鑫沐化工
实施例1
一种阻燃保温板,是以如下重量份的组分为原料制备而成的:
三聚氰胺氰尿酸盐溶液(MCA)5份、纳米碳管(CNTS)3份、高抗冲性聚苯乙烯(HIPS)30份、碳纤维10份、偶氮二甲酰胺10份、RFL浸渍液5份、硅烷偶联剂KH550 3份。
上述阻燃保温板的制备方法,该方法是通过如下步骤实现的:
(1)将纳米碳管溶于乙醇中,然后加入硅烷偶联剂KH550在55℃下搅拌4h;
(2)将经过步骤(1)处理的碳纳米管与高抗冲性聚苯乙烯在80℃、30r/min条件下于密炼机中共混15min,得到改性聚苯乙烯;
(3)将改性聚苯乙烯用饱和蒸汽加热后加入偶氮二甲酰胺,发泡4min后,熟化10h,得到发泡聚苯乙烯;
(4)将碳纤维剪切至1mm长的短碳纤维,然后浸到质量分数为62%的硝酸溶液中,在电解槽内进行阳极表面氧化处理,处理电压为4.5V,处理时间为15min,处理完成后取出烘干;
(5)将经过步骤(4)处理得到的短碳纤维在三聚氰胺氰尿酸盐溶液中浸泡8h后,取出烘干;
(6)将步骤(5)所得物质与浸渍液一同加入到步骤(2)得到的改性聚苯乙烯中混合均匀,然后通过模具成型,经过8天的养护后,切割成所需规格的阻燃保温板。
实施例2
一种阻燃保温板,是以如下重量份的组分为原料制备而成的:
三聚氰胺氰尿酸盐溶液(MCA)10份、纳米碳管(CNTS)5份、高抗冲性聚苯乙烯(HIPS)90份、碳纤维6份、二亚硝基五次甲基四胺5份、RFL浸渍液1份、硅烷偶联剂KH-560 2份。
上述阻燃保温板的制备方法,该方法是通过如下步骤实现的:
(1)将纳米碳管分散于乙醇中,然后加入硅烷偶联剂KH-560在65℃下搅拌2h;
(2)将经过步骤(1)处理的碳纳米管与高抗冲性聚苯乙烯在150℃、40r/min条件下于密炼机中共混10min,得到改性聚苯乙烯;
(3)将改性聚苯乙烯用饱和蒸汽加热后加入二亚硝基五次甲基四胺,发泡6min后,熟化8h,得到发泡聚苯乙烯;
(4)将碳纤维剪切至5mm长的短碳纤维,然后浸到质量分数为12%的酸性重铬酸钾溶液中,在电解槽内进行阳极表面氧化处理,处理电压为5.0V,处理时间为5min,处理完成后取出烘干;
(5)将经过步骤(4)处理得到的短碳纤维在三聚氰胺氰尿酸盐溶液中浸泡12h后,取出烘干;
(6)将步骤(5)所得物质与浸渍液一同加入到步骤(2)得到的改性聚苯乙烯中混合均匀,然后通过模具成型,经过10天的养护后,切割成所需规格的阻燃保温板。
实施例3
一种阻燃保温板,是以如下重量份的组分为原料制备而成的:
三聚氰胺氰尿酸盐溶液(MCA)1份、纳米碳管(CNTS)1份、高抗冲性聚苯乙烯(HIPS)70份、碳纤维1份、对甲苯酰胺肼1份、RFL浸渍液3份、硅烷偶联剂Si69 0.3份。
上述阻燃保温板的制备方法,该方法是通过如下步骤实现的:
(1)将纳米碳管分散于乙醇中,然后加入硅烷偶联剂Si69在60℃下搅拌3h;
(2)将经过步骤(1)处理的碳纳米管与高抗冲性聚苯乙烯在120℃、35r/min条件下于密炼机中共混12min,得到改性聚苯乙烯;
(3)将改性聚苯乙烯用饱和蒸汽加热后加入对甲苯酰胺肼,发泡5min后,熟化9h,得到发泡聚苯乙烯;
(4)将碳纤维剪切至3mm长的短碳纤维,然后浸到由质量分数为15%的次氯酸钠和质量分数为40%的硫酸按体积比为1:1混合得到的酸液中,在电解槽内进行阳极表面氧化处理,处理电压为4.8V,处理时间为10min,处理完成后取出烘干;
(5)将经过步骤(4)处理得到的短碳纤维在三聚氰胺氰尿酸盐溶液中浸泡10h后,取出烘干;
(6)将步骤(5)所得物质与浸渍液一同加入到步骤(2)得到的改性聚苯乙烯中混合均匀,然后通过模具成型,经过6天的养护后,切割成所需规格的阻燃保温板。
为了进一步对实施例1-3所得到的阻燃保温板的性能进行鉴定,还设置对比例1-7,其配方如表2所示,其中,对比例1和2的原料及制备方法与实施例1的制备方法相同,对比例3和4与实施例2的原料及制备方法相同,对比例5、6和7与实施例3的原料及制备方法相同。
表2对比例中配方
实施例材料性能测试
将所制得的样品测试各项强度如下。
表3:耐油橡胶密封材料浸油后各项性能测试
以上显示和描述了本发明的基本原理、主要特征和本发明的优点。本行业的技术人员应该了解,本发明不受上述实施例的限制,上述实施例和说明书中描述的只是本发明的原理,在不脱离本发明精神和范围的前提下本发明还会有各种变化和改进,这些变化和改进都落入要求保护的本发明的范围内。本发明要求的保护范围由所附的权利要求书及其等同物界定。

Claims (10)

1.一种阻燃保温板,其特征在于,是以如下重量份的组分为原料制备而成的:
2.如权利要求1所述阻燃保温板,其特征在于:所述浸渍液为RFL浸渍液。
3.如权利要求1所述阻燃保温板,其特征在于:所述发泡剂为偶氮二甲酰胺、二亚硝基五次甲基四胺、对甲苯酰胺肼中的一种或多种。
4.如权利要求1所述阻燃保温板,其特征在于:所述硅烷偶联剂为硅烷偶联剂KH550、硅烷偶联剂KH-560、硅烷偶联剂Si69中的一种或多种。
5.如权利要求1所述阻燃保温板,其特征在于:所述碳纤维的长度为1-5mm。
6.根据权利要求1-5所述阻燃保温板的制备方法,其特征在于,是通过如下步骤实现的:
(1)将纳米碳管分散于乙醇中,然后加入硅烷偶联剂在55-65℃下搅拌2-4h;
(2)将经过步骤(1)处理的碳纳米管与高抗冲性聚苯乙烯在80-150℃、30-40r/min条件下共混10-15min,得到改性聚苯乙烯;
(3)将改性聚苯乙烯用饱和蒸汽加热后加入发泡剂,发泡4-6min后,熟化8-10h,得到发泡聚苯乙烯;
(4)将碳纤维剪切至1-5mm长的短碳纤维,然后浸到酸性溶液中,在电解槽内进行阳极表面氧化处理,处理完成后取出烘干;
(5)将经过步骤(4)处理得到的短碳纤维在三聚氰胺氰尿酸盐溶液中浸泡8-12h后,
取出烘干;
(6)将步骤(5)所得物质与浸渍液一同加入到步骤(2)得到的改性聚苯乙烯中混合均匀,然后通过模具成型,切割成所需规格的阻燃保温板。
7.如权利要求6所述制备方法,其特征在于:步骤(4)中的酸性溶液为硝酸或酸性重铬酸钾或次氯酸钠与硫酸的混合液。
8.如权利要求6所述制备方法,其特征在于:步骤(4)中的处理电压为4.5-5.0V,处理时间为5-15min。
9.如权利要求8所述制备方法,其特征在于:步骤(4)中的处理电压为4.8V,处理时间为10min。
10.如权利要求6所述制备方法,其特征在于:步骤(6)中模具成型后,经过6-10天的养护后,再进行切割。
CN201710906439.4A 2017-09-29 2017-09-29 一种阻燃保温板及其制备方法 Active CN107522962B (zh)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201810285609.6A CN108822465B (zh) 2017-09-29 2017-09-29 一种阻燃保温板及其制备方法
CN201710906439.4A CN107522962B (zh) 2017-09-29 2017-09-29 一种阻燃保温板及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710906439.4A CN107522962B (zh) 2017-09-29 2017-09-29 一种阻燃保温板及其制备方法

Related Child Applications (1)

Application Number Title Priority Date Filing Date
CN201810285609.6A Division CN108822465B (zh) 2017-09-29 2017-09-29 一种阻燃保温板及其制备方法

Publications (2)

Publication Number Publication Date
CN107522962A true CN107522962A (zh) 2017-12-29
CN107522962B CN107522962B (zh) 2018-08-28

Family

ID=60683865

Family Applications (2)

Application Number Title Priority Date Filing Date
CN201710906439.4A Active CN107522962B (zh) 2017-09-29 2017-09-29 一种阻燃保温板及其制备方法
CN201810285609.6A Active CN108822465B (zh) 2017-09-29 2017-09-29 一种阻燃保温板及其制备方法

Family Applications After (1)

Application Number Title Priority Date Filing Date
CN201810285609.6A Active CN108822465B (zh) 2017-09-29 2017-09-29 一种阻燃保温板及其制备方法

Country Status (1)

Country Link
CN (2) CN107522962B (zh)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120112134A1 (en) * 2009-06-30 2012-05-10 Hanwha Chemical Corporation Blending Improvement Carbon-Composite having Carbon-Nanotube and its Continuous Manufacturing Method and Apparatus
CN103374200A (zh) * 2012-04-26 2013-10-30 合肥杰事杰新材料股份有限公司 一种高分子复合泡沫材料、制备方法及其应用
CN103834056A (zh) * 2014-02-27 2014-06-04 山东圣泉化工股份有限公司 聚苯乙烯保温板的生产方法
CN105585776A (zh) * 2016-03-23 2016-05-18 浙江润阳新材料科技股份有限公司 一种微波阻燃聚烯烃发泡材料及其制作方法
CN105647045A (zh) * 2016-03-10 2016-06-08 南京法宁格节能科技股份有限公司 复配阻燃聚苯乙烯颗粒及其制备方法
CN105906968A (zh) * 2016-06-29 2016-08-31 合肥广能新材料科技有限公司 聚苯乙烯复合保温材料及其制备方法
CN106810778A (zh) * 2016-12-29 2017-06-09 天津斯坦利新型材料有限公司 一种聚苯乙烯板的制备方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3163282B2 (ja) * 1998-06-12 2001-05-08 尊 藤森 発泡スチロール製品およびその製造方法
CN104629204A (zh) * 2015-02-13 2015-05-20 芜湖市伟华泡塑有限公司 一种改性发泡聚苯乙烯的制备方法
CN105218921B (zh) * 2015-09-30 2017-08-01 安徽酷米智能科技有限公司 一种手机屏安装用缓冲材料

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120112134A1 (en) * 2009-06-30 2012-05-10 Hanwha Chemical Corporation Blending Improvement Carbon-Composite having Carbon-Nanotube and its Continuous Manufacturing Method and Apparatus
CN103374200A (zh) * 2012-04-26 2013-10-30 合肥杰事杰新材料股份有限公司 一种高分子复合泡沫材料、制备方法及其应用
CN103834056A (zh) * 2014-02-27 2014-06-04 山东圣泉化工股份有限公司 聚苯乙烯保温板的生产方法
CN105647045A (zh) * 2016-03-10 2016-06-08 南京法宁格节能科技股份有限公司 复配阻燃聚苯乙烯颗粒及其制备方法
CN105585776A (zh) * 2016-03-23 2016-05-18 浙江润阳新材料科技股份有限公司 一种微波阻燃聚烯烃发泡材料及其制作方法
CN105906968A (zh) * 2016-06-29 2016-08-31 合肥广能新材料科技有限公司 聚苯乙烯复合保温材料及其制备方法
CN106810778A (zh) * 2016-12-29 2017-06-09 天津斯坦利新型材料有限公司 一种聚苯乙烯板的制备方法

Also Published As

Publication number Publication date
CN108822465B (zh) 2020-12-08
CN107522962B (zh) 2018-08-28
CN108822465A (zh) 2018-11-16

Similar Documents

Publication Publication Date Title
US20130274382A1 (en) Plate synthesized by waste circuit board powder and manufacturing process thereof
CN103556720B (zh) 一种墙体保温防火复合板
CN102690519A (zh) 一种低压缩应力松弛硅橡胶泡沫连续板材及其制备方法
CN101513744B (zh) 无醛环保型阻燃胶合板及其制造方法
CN106564235A (zh) 一种三聚氰胺纳米气凝胶co2发泡复合难燃闭孔硬质泡沫保温板及其制备方法
CN113338458A (zh) 一种阻燃型eps保温板及其制备方法
CN114133752A (zh) 一种耐高温隔热保温板及其制备方法
CN107556627A (zh) 发泡石墨烯/橡胶复合材料及其制备方法和应用
CN104647775A (zh) 一种阻燃改性轻质板材及其制备方法
CN102924864A (zh) 改性环保酚醛保温材料及其制备方法
CN106046671A (zh) 改性酚醛树脂复合保温材料及其制备方法
CN105174818A (zh) 一种石墨烯改性的浆体保温材料的制备方法
CN106433016A (zh) 一种改性增强型保温隔声酚醛泡沫板及其制备方法
CN107522962B (zh) 一种阻燃保温板及其制备方法
CN106217577A (zh) 一种高强度碳纤维木质复合纤维板及其制备方法
CN104829192B (zh) 保温隔热节能材料及其水泥板
CN107118412A (zh) 一种高效无卤阻燃的丁苯橡胶组合物及其制备方法
CN106084632A (zh) 一种有机/无机复合保温材料及制备方法
CN108117700B (zh) 阻燃柔性吸声材料及其制备方法和应用
CN107445512A (zh) 外墙阻燃聚苯保温材料及其制备方法
CN105255035A (zh) 一种聚苯乙烯改性耐热复合塑料
CN106750168A (zh) 一种阻燃硬质聚氨酯泡沫塑料的制备方法
CN112111128A (zh) 一种新型轨道车辆保温材料及其制备方法
Wang et al. Effects of scCO2 foaming process and post‐vulcanization method on cellular structure, mechanical properties, and thermal stability of PMVQ foams
CN106366560A (zh) 一种环氧改性抗压酚醛泡沫板及其制备方法

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
TA01 Transfer of patent application right
TA01 Transfer of patent application right

Effective date of registration: 20180719

Address after: 242000 Langxi County Economic Development Zone, Xuancheng, Anhui

Applicant after: ANHUI LONGDA BUILDING MATERIAL TECHNOLOGY CO.,LTD.

Address before: 315040 B3 building, R & D Park, Ningbo hi tech Development Zone, Zhejiang 509-512

Applicant before: ZHEJIANG DIHENG INDUSTRY Co.,Ltd.

GR01 Patent grant
GR01 Patent grant
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 kind of flame retardant insulation board and preparation method thereof

Effective date of registration: 20220919

Granted publication date: 20180828

Pledgee: Langxi SME Financing Guarantee Co.,Ltd.

Pledgor: ANHUI LONGDA BUILDING MATERIAL TECHNOLOGY CO.,LTD.

Registration number: Y2022980015508