CN113354909B - 一种发泡门封及其制备方法 - Google Patents

一种发泡门封及其制备方法 Download PDF

Info

Publication number
CN113354909B
CN113354909B CN202110705366.9A CN202110705366A CN113354909B CN 113354909 B CN113354909 B CN 113354909B CN 202110705366 A CN202110705366 A CN 202110705366A CN 113354909 B CN113354909 B CN 113354909B
Authority
CN
China
Prior art keywords
parts
extruder
foaming
door seal
stabilizer
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.)
Active
Application number
CN202110705366.9A
Other languages
English (en)
Other versions
CN113354909A (zh
Inventor
李方方
于静静
梁坤
马珺凤
高雷
李荣勋
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.)
Qingdao Jiesheng New Material Technology Co ltd
Original Assignee
Qingdao Jiesheng New Material Technology 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 Qingdao Jiesheng New Material Technology Co ltd filed Critical Qingdao Jiesheng New Material Technology Co ltd
Priority to CN202110705366.9A priority Critical patent/CN113354909B/zh
Publication of CN113354909A publication Critical patent/CN113354909A/zh
Application granted granted Critical
Publication of CN113354909B publication Critical patent/CN113354909B/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
    • 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
    • C08J9/0014Use of organic additives
    • C08J9/0023Use of organic additives containing oxygen
    • 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
    • C08J9/0066Use of inorganic 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
    • C08J9/0095Mixtures of at least two compounding ingredients belonging to different one-dot groups
    • 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
    • C08J2205/00Foams characterised by their properties
    • C08J2205/04Foams characterised by their properties characterised by the foam pores
    • C08J2205/044Micropores, i.e. average diameter being between 0,1 micrometer and 0,1 millimeter
    • 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
    • C08J2327/00Characterised 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 a halogen; Derivatives of such polymers
    • C08J2327/02Characterised 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment
    • C08J2327/04Characterised 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 a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08J2327/06Homopolymers or copolymers of vinyl chloride
    • 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
    • C08J2423/00Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
    • C08J2423/02Characterised 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
    • C08J2423/04Homopolymers or copolymers of ethene
    • C08J2423/06Polyethene
    • 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
    • C08J2467/00Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
    • 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
    • C08J2491/00Characterised by the use of oils, fats or waxes; Derivatives thereof
    • C08J2491/06Waxes
    • 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
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/24Acids; Salts thereof
    • C08K3/26Carbonates; Bicarbonates
    • C08K2003/265Calcium, strontium or barium carbonate
    • 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
    • C08K3/30Sulfur-, selenium- or tellurium-containing compounds
    • C08K2003/3045Sulfates
    • 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
    • C08K3/34Silicon-containing compounds
    • 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
    • C08K5/00Use of organic ingredients
    • C08K5/04Oxygen-containing compounds
    • C08K5/10Esters; Ether-esters
    • C08K5/12Esters; Ether-esters of cyclic polycarboxylic acids
    • 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
    • C08K5/00Use of organic ingredients
    • C08K5/16Nitrogen-containing compounds
    • C08K5/20Carboxylic acid amides
    • 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
    • C08K7/00Use of ingredients characterised by shape
    • C08K7/22Expanded, porous or hollow particles
    • C08K7/24Expanded, porous or hollow particles inorganic

Abstract

本发明公开了一种发泡门封及其制备方法,包括以下组分:PVC树脂粉80‑100份、增塑剂50‑70份、发泡剂20‑30份、填充剂20‑50份、润滑剂0.2‑0.5份、稳定剂2‑5份、抗氧剂0.2‑0.5份、抗菌防霉剂1‑2份,发泡剂为改性石墨烯气凝胶粉末。本申请以改性石墨烯气凝胶为发泡剂,对PVC树脂进行发泡,改性石墨烯气凝胶不仅是本方案中的发泡剂,而且由二维片层状的改性石墨烯搭接而成的三维交联网络骨架结构具有超弹性,因此解决了传统发泡剂和二氧化硅气凝胶均不能解决的发泡门封抗压能力差,气泡容易破碎的问题。

Description

一种发泡门封及其制备方法
技术领域
本发明属于发泡门封技术领域,涉及改性石墨烯气凝胶发泡门封及其制备方法
技术背景
随着全球能源的消耗及人们低碳节能意识的提高,各国相继对冰箱等家电设备提出了更高的能耗标准要求。如欧盟ERP指令、中国最新能耗等级的修订、欧盟市场A+++能耗等级的推广实施等。
在影响冰箱能耗的诸多因素中门封是关键因素之一,为提高门封的密封隔热性能、降低冰箱耗电量,使其达到更高的能效要求,通常可通过调整门封结构特性、改善升级原材料配方等方法来实现。
现有不发泡的门封条热导率通常为0.25W/(m·K),为了寻求更低的热导系数,市场出现了发泡门封,常规泡沫塑料的泡孔直径一般大于50mm,泡孔的密度(单位体积内泡孔的数量)小于106个/cm3。常规发泡门封由于泡孔直径较大,这些大尺寸的泡孔受力时常常成为初始裂纹的发源地,降低了材料的机械性能。
发明内容
本发明的目的是供一种发泡门封及其制备方法,本申请以改性石墨烯气凝胶为发泡剂,对PVC树脂进行发泡,改性石墨烯气凝胶不仅是本方案中的发泡剂,而且由二维片层状的改性石墨烯搭接而成的三维交联网络骨架结构具有超弹性,因此解决了传统发泡剂和二氧化硅气凝胶均不能解决的发泡门封抗压能力差,气泡容易破碎的问题。为了实现上述目的,本发明提供如下技术方案:
一种发泡门封,按照重量份数,包括以下组分:
所述发泡剂为改性石墨烯气凝胶粉末。
优选地,所述增塑剂为聚酯或TOTM增塑剂。
优选地,所述填充剂为碳酸钙、滑石粉、硫酸钡中的一种或几种。
优选地,所述润滑剂为费托蜡、聚乙烯蜡、油酸酰胺中的一种或两种。
优选地,所述稳定剂为钙/锌复合稳定剂、有机锡稳定剂、沸石类铝镁稳定剂中的一种或多种。
优选地,所述PVC树脂粉的聚合度≥1300。
另外,本申请还提供一种制备如上述的发泡门封的方法,包括以下步骤:
将PVC树脂粉和增塑剂按照配方用量称量,将混合均匀的PVC树脂粉和增塑剂加入高速搅拌机250-350r/min搅拌30min,升温至90℃,然后加入发泡剂、填充剂、稳定剂、抗氧剂、防霉抗菌剂和润滑剂,450-550r/min搅拌,继续升温至125℃,均匀后放入冷搅锅降温60-70℃;将上述PVC料加入挤出机挤出造粒,得到PVC微孔结构母粒,挤出成型,得到门封条。
优选地,所述挤出成型是指将PVC微孔结构母粒送入挤出机中挤出成型,对挤出机中十一个区与机头进行控温,挤出机中一区温度为100-110℃,二区至八区温度为115-125℃,九区至十一区温度为105-115℃,机头温度为100-120℃。
优选地,所述挤出机为双螺杆挤出机,转速150-170r/min。
优选地,所述挤出机为单螺杆挤出机,转速20-30r/min。
本发明的有益效果:
1、改性后的具有微孔结构的PVC发泡门封,热导率明显下降,是常规PVC的70%,提高了门封的隔热保温效果,而且可降低门封比重,减少生产成本。
2、PVC门封中加入改性石墨烯气凝胶后,冰箱的降温速度加快10%,停止运行后的升温速度比正常PVC的慢5%,整机能耗降低3%。
3、改性石墨烯气凝胶的表面能很高,能够对增塑剂产生吸附作用,从而降低增塑剂迁移,进而降低因增塑剂迁移产生的制冷设备难开门以及污染食品、有害健康的风险。
4、改性石墨烯气凝胶既可以起到发泡的作用,而且可替代部分填充剂,起到事半功倍的效果。
附图说明
图1是本申请实施例3制备得到的发泡门封显微镜照片。
图2是本申请对照组1制备得到的发泡门封显微镜照片。
具体实施方式
实施例1
一种发泡门封,按照重量份数,包括以下组分:
发泡剂为改性石墨烯气凝胶粉末,具体为氧化石墨烯气凝胶,粒径为20μm。增塑剂为聚酯增塑剂。填充剂为碳酸钙。润滑剂为费托蜡。稳定剂为钙/锌复合稳定剂。
PVC树脂粉的聚合度≥1300。
一种制备如上述的发泡门封的方法,包括以下步骤:
将PVC树脂粉和增塑剂按照配方用量称量,将混合均匀的PVC树脂粉和增塑剂加入高速搅拌机350r/min搅拌30min,升温至90℃,然后加入发泡剂、填充剂、稳定剂、抗氧剂、防霉抗菌剂和润滑剂,550r/min搅拌,继续升温至125℃,均匀后放入冷搅锅降温70℃;将上述PVC料加入挤出机挤出造粒,得到PVC微孔结构母粒,挤出成型,得到门封条。
所述挤出成型是指将PVC微孔结构母粒送入挤出机中挤出成型,对挤出机中十一个区与机头进行控温,挤出机中一区温度为100℃,二区至八区温度为115℃,九区至十一区温度为105℃,机头温度为100℃。挤出机为双螺杆挤出机,转速150r/min。
实施例2
一种发泡门封,按照重量份数,包括以下组分:
发泡剂为改性石墨烯气凝胶粉末,具体为N杂化石墨烯气凝胶,粒径为20μm。增塑剂为TOTM增塑剂。填充剂为碳酸钙和硫酸钡。润滑剂为费托蜡和聚乙烯蜡。稳定剂为钙/锌复合稳定剂和有机锡稳定剂。
PVC树脂粉的聚合度≥1300。
一种制备如上述的发泡门封的方法,包括以下步骤:
将PVC树脂粉和增塑剂按照配方用量称量,将混合均匀的PVC树脂粉和增塑剂加入高速搅拌机250r/min搅拌30min,升温至90℃,然后加入发泡剂、填充剂、稳定剂、抗氧剂、防霉抗菌剂和润滑剂,450r/min搅拌,继续升温至125℃,均匀后放入冷搅锅降温60℃;将上述PVC料加入挤出机挤出造粒,得到PVC微孔结构母粒,挤出成型,得到门封条。
所述挤出成型是指将PVC微孔结构母粒送入挤出机中挤出成型,对挤出机中十一个区与机头进行控温,挤出机中一区温度为110℃,二区至八区温度为125℃,九区至十一区温度为115℃,机头温度为120℃。挤出机为单螺杆挤出机,转速20r/min。
实施例3
一种发泡门封,按照重量份数,包括以下组分:
发泡剂为改性石墨烯气凝胶粉末,具体为硫化石墨烯气凝胶,粒径为20μm。增塑剂为聚酯增塑剂和TOTM增塑剂。填充剂为滑石粉。润滑剂为油酸酰胺。稳定剂为沸石类铝镁稳定剂和有机锡稳定剂。
PVC树脂粉的聚合度≥1300。
一种制备如上述的发泡门封的方法,包括以下步骤:
将PVC树脂粉和增塑剂按照配方用量称量,将混合均匀的PVC树脂粉和增塑剂加入高速搅拌机330r/min搅拌30min,升温至90℃,然后加入发泡剂、填充剂、稳定剂、抗氧剂、防霉抗菌剂和润滑剂,500r/min搅拌,继续升温至125℃,均匀后放入冷搅锅降温65℃;将上述PVC料加入挤出机挤出造粒,得到PVC微孔结构母粒,挤出成型,得到门封条。
所述挤出成型是指将PVC微孔结构母粒送入挤出机中挤出成型,对挤出机中十一个区与机头进行控温,挤出机中一区温度为105℃,二区至八区温度为120℃,九区至十一区温度为110℃,机头温度为110℃。双螺杆挤出机,转速160r/min。
对照组1:
对照组发泡剂采用二氧化硅气凝胶,按照重量份数,包括以下组分:
其他实验条件与实施例3相同。
对实施例1、实施例2、实施例3和对照组1制备的发泡门封的热导率和机械性能等进行检测,检测结果如下表1:
表1
通过上述测试可以看出,本申请实施例的门封条无论拉伸强度还是撕裂强度都明显优于对照组,这是因为改性石墨烯气凝胶发泡均匀,不容易出现应力集中点,在受到压缩应力后,具有较好的弹性。同时石墨烯气凝胶具有更低的导热系数,因而门封具有更低的传热速率,同时PVC门封中加入改性石墨烯气凝胶后,冰箱的降温速度加快10%,停止运行后的升温速度比正常PVC的慢5%,整机能耗降低3%。
从图1和图2可以看出,本实施例3使用改性石墨烯发泡后,泡孔大小适中,分布也较为均匀,表面光滑,破裂极少;而使用二氧化硅气凝胶发泡后,泡孔连成一片,大小不均,互相重叠,泡孔破裂较多。泡孔破裂是导致其力学性能和导热系数下降的主要原因。
此外,应当理解,虽然本说明书按照实施方式加以描述,但并非每个实施方式仅包含一个独立的技术方案,说明书的这种叙述方式仅仅是为清楚起见,本领域技术人员应当将说明书作为一个整体,各实施例中的技术方案也可以经适当组合,形成本领域技术人员可以理解的其他实施方式。

Claims (7)

1.一种发泡门封,其特征在于,按照重量份数,由以下组分构成:
PVC树脂粉80-100份,增塑剂50-70份,发泡剂10-20份,填充剂20-50份,润滑剂0.2-0.5份,稳定剂2-5份,抗氧剂0.2-0.5份,抗菌防霉剂1-2份;
所述发泡剂为改性石墨烯气凝胶粉末,改性石墨烯气凝胶是由二维片层状的改性石墨烯搭接而成的三维交联网络骨架结构;所述改性石墨烯气凝胶为氧化石墨烯气凝胶、N杂化石墨烯气凝胶、硫化石墨烯气凝胶中的一种;所述填充剂为碳酸钙、滑石粉、硫酸钡中的一种或几种,所述润滑剂为费托蜡、聚乙烯蜡、油酸酰胺中的一种或两种,所述稳定剂为钙/锌复合稳定剂、有机锡稳定剂、沸石类铝镁稳定剂中的一种或多种。
2.根据权利要求1所述的发泡门封,其特征在于,所述增塑剂为聚酯或TOTM增塑剂。
3.根据权利要求1所述的发泡门封,其特征在于,所述PVC树脂粉的聚合度≥1300。
4.一种制备如权利要求1-3任一所述的发泡门封的方法,其特征在于,包括以下步骤:
将PVC树脂粉和增塑剂按照配方用量称量,将混合均匀的PVC树脂粉和增塑剂加入高速搅拌机250-350 r/min搅拌30 min,升温至90℃,然后加入发泡剂、填充剂、稳定剂、抗氧剂、防霉抗菌剂和润滑剂,450-550 r/min搅拌,继续升温至125℃,均匀后放入冷搅锅降温60-70℃;将上述PVC料加入挤出机挤出造粒,得到PVC微孔结构母粒,挤出成型,得到门封条。
5.根据权利要求4所述的发泡门封的制备方法,其特征在于,所述挤出成型是指将PVC微孔结构母粒送入挤出机中挤出成型,对挤出机中十一个区与机头进行控温,挤出机中一区温度为100-110℃,二区至八区温度为115-125℃,九区至十一区温度为105-115℃,机头温度为100-120℃。
6.根据权利要求4所述的发泡门封的制备方法,其特征在于,所述挤出机为双螺杆挤出机,转速150-170 r/min。
7.根据权利要求4所述的发泡门封的制备方法,其特征在于,所述挤出机为单螺杆挤出机,转速20-30 r/min。
CN202110705366.9A 2021-06-24 2021-06-24 一种发泡门封及其制备方法 Active CN113354909B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110705366.9A CN113354909B (zh) 2021-06-24 2021-06-24 一种发泡门封及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110705366.9A CN113354909B (zh) 2021-06-24 2021-06-24 一种发泡门封及其制备方法

Publications (2)

Publication Number Publication Date
CN113354909A CN113354909A (zh) 2021-09-07
CN113354909B true CN113354909B (zh) 2023-09-01

Family

ID=77536343

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110705366.9A Active CN113354909B (zh) 2021-06-24 2021-06-24 一种发泡门封及其制备方法

Country Status (1)

Country Link
CN (1) CN113354909B (zh)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106609011A (zh) * 2015-10-21 2017-05-03 大电塑料(上海)有限公司 一种发泡pvc材料及其制备方法和用途
CN106832679A (zh) * 2017-03-09 2017-06-13 江苏云腾高新科技有限公司 一种高耐热pvc发泡型材及制备方法
CN107619548A (zh) * 2016-07-13 2018-01-23 江阴市志远汽车饰件有限公司 一种高强度塑胶地板及其制备方法
CN109096658A (zh) * 2018-09-11 2018-12-28 界首永恩机电科技有限公司 一种改性pvc粒料及其制备方法
CN109096647A (zh) * 2018-08-01 2018-12-28 安徽邦瑞新材料科技有限公司 一种手感爽滑细腻pvc门封材料及制备方法
CN110655634A (zh) * 2019-11-13 2020-01-07 万华化学集团股份有限公司 高阻燃聚氨酯泡沫组合料及其制成的高阻燃聚氨酯泡沫
CN111471251A (zh) * 2020-05-14 2020-07-31 素湃科技(上海)有限公司 一种含气凝胶隔热材料及其制备方法

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106609011A (zh) * 2015-10-21 2017-05-03 大电塑料(上海)有限公司 一种发泡pvc材料及其制备方法和用途
CN107619548A (zh) * 2016-07-13 2018-01-23 江阴市志远汽车饰件有限公司 一种高强度塑胶地板及其制备方法
CN106832679A (zh) * 2017-03-09 2017-06-13 江苏云腾高新科技有限公司 一种高耐热pvc发泡型材及制备方法
CN109096647A (zh) * 2018-08-01 2018-12-28 安徽邦瑞新材料科技有限公司 一种手感爽滑细腻pvc门封材料及制备方法
CN109096658A (zh) * 2018-09-11 2018-12-28 界首永恩机电科技有限公司 一种改性pvc粒料及其制备方法
CN110655634A (zh) * 2019-11-13 2020-01-07 万华化学集团股份有限公司 高阻燃聚氨酯泡沫组合料及其制成的高阻燃聚氨酯泡沫
CN111471251A (zh) * 2020-05-14 2020-07-31 素湃科技(上海)有限公司 一种含气凝胶隔热材料及其制备方法

Also Published As

Publication number Publication date
CN113354909A (zh) 2021-09-07

Similar Documents

Publication Publication Date Title
CN102911430B (zh) 一种eva/tpu/poe复合发泡材料的制备方法
CN104072881B (zh) 一种热塑性微发泡减震材料及其制备方法
CN103397707B (zh) 多层铝塑复合阻燃保温隔热材料四段式生产工艺
CN105885250B (zh) 三元乙丙橡胶微孔垫板的生产工艺及其产品
CN111471251A (zh) 一种含气凝胶隔热材料及其制备方法
CN106496856A (zh) 微发泡材料及其制备方法和制冷设备
CN111393812A (zh) 一种pla/eva超临界发泡复合材料及其制备方法
CN113354909B (zh) 一种发泡门封及其制备方法
CN105419155A (zh) 一种高耐候性的改性塑料
CN102604205B (zh) 一种环保复合增强聚丙烯建筑模板
CN102558709A (zh) 一种软质聚氯乙烯发泡材料及其成型方法
CN108912380A (zh) 一种低压条件下利用pmma/pvdf共混物制备大倍率聚合物泡沫的方法
CN105218938A (zh) 一种跳高垫用eva复合材料及其制备方法
CN112778619A (zh) 一种超轻eva复合材料及其制备方法和应用
CN103420664A (zh) 一种无机蜂巢硬化保温材料及其生产方法
CN103865204B (zh) 一种聚氯乙烯管材的制备方法
CN108676281A (zh) 一种制备高温耐磨交联聚氯乙烯板材的方法
CN107163466A (zh) 一种环保型保温材料及其制备方法
CN104763862B (zh) 一种真空隔热板及其制备方法
CN106905586A (zh) 微发泡功能母粒组合物及其制备方法以及冰箱发泡板
CN106700343A (zh) 改性pvc墙板及其制备方法
CN201648600U (zh) 超高分子量聚乙烯熔体的静态混合器
CN108517090A (zh) 一种制备低温高硬度聚氯乙烯结皮发泡板材的方法
CN108517095A (zh) 一种制备高硬度耐磨聚氯乙烯结皮发泡板材的方法
CN109265806A (zh) 一种pe保鲜膜母料的制备方法

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

Effective date of registration: 20230717

Address after: No. 10 Zhenyuan Road, Houhaixi Community, Jihongtan Street, Chengyang District, Qingdao City, Shandong Province, 266000

Applicant after: Qingdao Jiesheng New Material Technology Co.,Ltd.

Address before: 266100 in Qingda Industrial Park, Qingdao, Shandong Province

Applicant before: QINGDAO NEW MATERIAL TECHNOLOGY INDUSTRIAL PARK DEVELOPMENT Co.,Ltd.

GR01 Patent grant
GR01 Patent grant