CN110272552B - 一种石墨烧结用聚酰亚胺薄膜的制备方法 - Google Patents

一种石墨烧结用聚酰亚胺薄膜的制备方法 Download PDF

Info

Publication number
CN110272552B
CN110272552B CN201910537474.2A CN201910537474A CN110272552B CN 110272552 B CN110272552 B CN 110272552B CN 201910537474 A CN201910537474 A CN 201910537474A CN 110272552 B CN110272552 B CN 110272552B
Authority
CN
China
Prior art keywords
polyimide film
resin
controlling
film
steps
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
CN201910537474.2A
Other languages
English (en)
Other versions
CN110272552A (zh
Inventor
程翠华
陈胜绪
李开明
张彩霞
刘丹丹
赵春晖
马志远
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.)
Fuyoute (Shandong) new material technology Co.,Ltd.
Original Assignee
Qingdao Cosm New 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 Qingdao Cosm New Materials Co ltd filed Critical Qingdao Cosm New Materials Co ltd
Priority to CN201910537474.2A priority Critical patent/CN110272552B/zh
Publication of CN110272552A publication Critical patent/CN110272552A/zh
Application granted granted Critical
Publication of CN110272552B publication Critical patent/CN110272552B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/20Graphite
    • C01B32/205Preparation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1042Copolyimides derived from at least two different tetracarboxylic compounds or two different diamino compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1046Polyimides containing oxygen in the form of ether bonds in the main chain
    • C08G73/105Polyimides containing oxygen in the form of ether bonds in the main chain with oxygen only in the diamino moiety
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1067Wholly aromatic polyimides, i.e. having both tetracarboxylic and diamino moieties aromatically bound
    • C08G73/1071Wholly aromatic polyimides containing oxygen in the form of ether bonds in the main chain
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1075Partially aromatic polyimides
    • 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
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • 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
    • C08K3/32Phosphorus-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
    • 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
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/38Boron-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
    • C08K7/00Use of ingredients characterised by shape
    • 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
    • C08J2379/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2361/00 - C08J2377/00
    • C08J2379/04Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
    • C08J2379/08Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • 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
    • C08K3/32Phosphorus-containing compounds
    • C08K2003/321Phosphates
    • C08K2003/325Calcium, strontium or barium phosphate
    • 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
    • C08K3/38Boron-containing compounds
    • C08K2003/382Boron-containing compounds and nitrogen
    • C08K2003/385Binary compounds of nitrogen with boron

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)

Abstract

本发明涉及聚酰亚胺薄膜制备领域,尤其是一种石墨烧结用聚酰亚胺薄膜的制备方法。本发明的一种石墨烧结用聚酰亚胺薄膜的制备方法,通过将芳香族二胺溶于极性溶剂中,再与芳香族二酐聚合制得聚酰亚胺酸树脂,并在树脂合成过程中中引入导热材料,引导树酯固化和亚胺化时分子链沿二维排布均匀趋向排列,利于高温烧结时六角二维碳平面生长,避免因为聚酰亚胺薄膜热缩和结构问题带来的石墨膜褶皱不平和导热率低等问题,解决烧结石墨热缩大、褶皱多、导热率低等问题,使得到的聚酰亚胺薄膜经高温烧结后得到,表面平整、细腻,导热率达到1500W/MK以上。

Description

一种石墨烧结用聚酰亚胺薄膜的制备方法
技术领域
本发明涉及聚酰亚胺薄膜制备领域,尤其是一种石墨烧结用聚酰亚胺薄膜的制备方法。
背景技术
聚酰亚胺作为高强高模耐候性材料,在电子器件、航天飞行器等先进行业领域被广泛关注和热捧。聚酰亚胺薄膜的一般制备方法为:聚酰胺酸溶液流延成膜、拉伸后,高温酰亚胺化。薄膜呈黄色透明,相对密度1.39-1.45,有突出的耐高温、耐辐射、耐化学腐蚀和电绝缘性能,可在250-280℃空气中长期使用。玻璃化温度分别为280℃(Upilex R)、385℃(Kapton)和500℃以上(Upilex S)。20℃时拉伸强度为200MPa,200℃时大于100MPa。特别适宜用作柔性印制电路板基材和各种耐高温电机电器绝缘材料。
聚酰亚胺石墨化在一定温度下发生高温分解,高分子链重排形成六角炭结构,并按规整六角炭网生长形成石墨材料。科研人员研究聚酰亚胺薄膜石墨化过程,发现聚酰亚胺薄膜热缩不均、褶皱严重、导热率低。我国聚酰亚胺薄膜多用予绝缘行业,烧结用聚酰亚胺薄膜主要依赖进口。
因此,提供一种一种石墨烧结用聚酰亚胺薄膜的制备方法,产品热缩均匀、表面平整、结构致密、导热性佳,是本领域技术人员亟待解决的技术问题。
发明内容
本发明的目的在于提供一种石墨烧结用聚酰亚胺薄膜的制备方法,免因为聚酰亚胺薄膜热缩和结构问题带来的石墨膜褶皱不平和导热率低等问题,解决烧结石墨热缩大、褶皱多、导热率低等问题。
本发明解决其技术问题所采取的技术方案是:
一种石墨烧结用聚酰亚胺薄膜的制备方法,包括如下步骤:
(1)取芳香族二胺溶于极性溶剂中,取芳香族二酐加入溶于极性溶剂中的芳香族二胺中进行树脂合成,树脂起粘后加入导热材料,导热材料在树脂合成过程中均匀分散,控制树脂合成温度不超过65℃,树脂合成时间为2-16h,导热材料加入后分散时间不低于2h,最终酐与胺的摩尔比控制在0.95-1.03,最终粘度控制在40-480pa.s,调粘时间为3.5-4.5h,整个调粘过程树脂温度控制在30-60℃;
(2)步骤(1)中合成好的树脂经脱泡过滤后,通过刮涂、辊涂或挤压涂覆,均匀涂覆在运转的模具(例如钢带)表面,在120-250℃条件下干燥成膜,成膜后残留极性溶剂含量约60-90%;
(3)将步骤(2)干燥后的薄膜牵引入双向拉伸机,在(0.8-1.3):1的牵伸条件下进行热法亚胺化,控制亚胺化过程温度在360-450℃,控制拉伸机进口温度100-160℃,出口温度80-250℃,制得平整均匀的聚酰亚胺薄膜,经逐步升温至2800-2900℃烧结,即得。
优选的,所述芳香族二胺为4,4-二氨基二苯醚(ODA)、丙二胺(PDA)、2,2'-三氟甲基二氨基联苯-4,4'-二氨基联苯(TFDB)和4,4'-二氨基二苯基甲烷(MDA)中的一种或几种组合而成。
优选的,所述芳香族二酐是3,3’,4,4’-联苯四甲酸二酐(BPDA)、1,2,4,5-均苯四甲酸二酐(PMDA)、4,4'-氧双邻苯二甲酸酐(ODPA)、3,3’,4,4’---二苯酮四酸二酐(BTDA)中的一种或几种组合而成。
优选的,所述极性溶剂为二甲基乙酰胺(DMAC) 、二甲基甲酰胺(DMF)或N-甲基吡咯烷酮(NMP)中的一种。
优选的,所述导热材料为碳化硅、氮化硼、氮化铝、钙磷化合物中的一种或几种组合而成;导热材料的使用质量是树脂固体质量的0.05-8%。
优选的,所述导热材料使用前进行预处理,所述预处理包括如下步骤:
S1:将导热材料在105-110℃条件下,干燥3-5h;
S2:干燥后的导热材料进行研磨至粒径为10nm-10um。
优选的,所述步骤(1)中极性溶剂的质量是二胺与二酐总质量的4-7倍。
本发明的有益效果是:与现有技术相比,本发明的一种石墨烧结用聚酰亚胺薄膜的制备方法,通过将芳香族二胺溶于极性溶剂中,再与芳香族二酐聚合制得聚酰亚胺酸树脂,并在树脂合成过程中中引入导热材料,引导树酯固化和亚胺化时分子链沿二维排布均匀趋向排列,利于高温烧结时六角二维碳平面生长,避免因为聚酰亚胺薄膜热缩和结构问题带来的石墨膜褶皱不平和导热率低等问题,解决烧结石墨热缩大、褶皱多、导热率低等问题,使得到的聚酰亚胺薄膜经高温烧结后得到,表面平整、细腻,导热率达到1500W/MK以上。
具体实施方式
实施例1
一种石墨烧结用聚酰亚胺薄膜的制备方法,包括如下步骤:
(1)取100.12kg ODA溶于900kg DMAC中,取109.6kg PMDA加入溶于极性溶剂中的ODA中进行树脂合成,树脂起粘后加入650g粒径为500nm的氮化硼片状颗粒,氮化硼片状颗粒在树脂合成过程中均匀分散,控制树脂合成温度不超过65℃,树脂合成时间为6h,导热材料加入后分散时间不低于2h,最终酐与胺的摩尔比控制在0.985:1,最终粘度控制在120pa.s,调粘时间为4h,整个调粘过程树脂温度控制在30-60℃内;
(2)步骤(1)中合成好的树脂经脱泡过滤后,通过刮板刀均匀涂覆在运转的钢带表面,在180℃条件下干燥成膜,成膜后残留极性溶剂含量约79%;
(3)将步骤(2)干燥后的薄膜牵引入双向拉伸机,在1:1的牵伸条件下进行热法亚胺化,控制亚胺化过程温度在380℃,控制拉伸机进口温度150℃,出口温度180℃,制得平整均匀的聚酰亚胺薄膜,拉伸强度248MPA,经逐步升温至2860℃烧结,即得表面平整,导热率1520W/MK的石墨膜。
本实施例中,所述导热材料使用前进行预处理,所述预处理包括如下步骤:
S1:将导热材料在108℃条件下,干燥4h;
S2:干燥后的导热材料进行研磨至粒径为500nm。
实施例2
一种石墨烧结用聚酰亚胺薄膜的制备方法,包括如下步骤:
(1)取100.12kg ODA和54.07kgPDA溶于1500kgDMAC中,取218.12kgPMDA加入溶于极性溶剂中的ODA和PDA中进行树脂合成,树脂起粘后加入1.3kg粒径为100nm的碳化硅颗粒,碳化硅颗粒在树脂合成过程中均匀分散,控制树脂合成温度不超过65℃,树脂合成时间为6h,导热材料加入后分散时间不低于2h,最终酐与胺的摩尔比控制在0.995:1,最终粘度控制在120pa.s,调粘时间为4h,整个调粘过程树脂温度控制在30-60℃内;
(2)步骤(1)中合成好的树脂经脱泡过滤后,通过刮板刀均匀涂覆在运转的钢带表面,在180℃条件下干燥成膜,成膜后残留极性溶剂含量为82%;
(3)将步骤(2)干燥后的薄膜牵引入双向拉伸机,在1:1的牵伸条件下进行热法亚胺化,控制亚胺化过程温度在390℃,控制拉伸机进口温度130℃,出口温度200℃,制得平整均匀的聚酰亚胺薄膜,测得拉伸强度236MPA,经逐步升温至2828℃烧结,得到表面平整导热率1560W/MK的石墨膜。
本实施例中,所述导热材料使用前进行预处理,所述预处理包括如下步骤:
S1:将导热材料在108℃条件下,干燥4h;
S2:干燥后的导热材料进行研磨至粒径为100nm。
实施例3
一种石墨烧结用聚酰亚胺薄膜的制备方法,包括如下步骤:
(1)取100.12kg ODA溶于900kg NMP中,取109.06kg PMDA加入溶于极性溶剂中的ODA中进行树脂合成,树脂起粘后加入1.2kg粒径为1000nm的磷酸氢钙颗粒,磷酸氢钙颗粒在树脂合成过程中均匀分散,控制树脂合成温度不超过65℃,树脂合成时间为6h,导热材料加入后分散时间不低于2h,最终酐与胺的摩尔比控制在0.995:1,最终粘度控制在120pa.s,调粘时间为4h,整个调粘过程树脂温度控制在30-60℃内;
(2)步骤(1)中合成好的树脂经脱泡过滤后,通过刮板刀均匀涂覆在运转的钢带表面,在200℃条件下干燥成膜,成膜后残留极性溶剂含量为75%;
(3)将步骤(2)干燥后的薄膜牵引入双向拉伸机,在1:0.9的牵伸条件下进行热法亚胺化,控制亚胺化过程温度在420℃,控制拉伸机进口温度150℃,出口温度230℃,制得平整均匀的聚酰亚胺薄膜,经检测拉伸强度229MPA,经逐步升温至2880℃烧结,得到表面平整导热率1580W/MK的石墨膜。
本实施例中,所述导热材料使用前进行预处理,所述预处理包括如下步骤:
S1:将导热材料在108℃条件下,干燥4h;
S2:干燥后的导热材料进行研磨至粒径为1000nm。
对比例1
对比例1与实施例3基本相同,其区别在于:导热材料预处理过程中未经过干燥,直接研磨至粒径为1000nm。
对比例1中制得平整均匀的聚酰亚胺薄膜,经检测拉伸强度183MPA,经逐步升温至2880℃烧结,得到表面平整度明显低于实施例3且导热率1468W/MK的石墨膜。
对比例1制得的聚酰亚胺薄膜在烧结前拉伸强度明显低于实施例3,烧结后其表面平整度降低,导热率降低。
上述具体实施方式仅是本发明的具体个案,本发明的专利保护范围包括但不限于上述具体实施方式的产品形态和式样,任何符合本发明权利要求书且任何所属技术领域的普通技术人员对其所做的适当变化或修饰,皆应落入本发明的专利保护范围。

Claims (6)

1.一种石墨烧结用聚酰亚胺薄膜的制备方法,其特征在于:包括如下步骤:
(1)取芳香族二胺溶于极性溶剂中,取芳香族二酐加入溶于极性溶剂中的芳香族二胺中进行树脂合成,树脂起粘后加入导热材料,导热材料在树脂合成过程中均匀分散,控制树脂合成温度不超过65℃,树脂合成时间为2-16h,导热材料加入后分散时间不低于2h,最终酐与胺的摩尔比控制在0.95-1.03,最终粘度控制在40-480pa.s,调粘时间为3.5-4.5h,整个调粘过程树脂温度控制在30-70℃;
(2)步骤(1)中合成好的树脂经脱泡过滤后,通过刮涂、辊涂或挤压涂覆,均匀涂覆在运转的模具表面,在120-250℃条件下干燥成膜,成膜后残留极性溶剂含量为60-90%;
(3)将步骤(2)干燥后的薄膜牵引入双向拉伸机,在(0.8-1.3):1的牵伸条件下进行热法亚胺化,控制亚胺化过程温度在360-450℃,控制拉伸机进口温度100-160℃,出口温度80-250℃,制得平整均匀的聚酰亚胺薄膜,经逐步升温至2800-2900℃烧结,即得;
所述导热材料使用前进行预处理,所述预处理包括如下步骤:
S1:将导热材料在105-110℃条件下,干燥3-5h;
S2:干燥后的导热材料进行研磨至粒径为10nm-10um。
2.根据权利要求1所述的一种石墨烧结用聚酰亚胺薄膜的制备方法,其特征在于:所述芳香族二胺为4,4-二氨基二苯醚(ODA)、2,2'-三氟甲基二氨基联苯-4,4'-二氨基联苯(TFDB)和4,4'-二氨基二苯基甲烷(MDA)中的一种或几种组合而成。
3.根据权利要求1所述的一种石墨烧结用聚酰亚胺薄膜的制备方法,其特征在于:所述芳香族二酐是3,3’,4,4’-联苯四甲酸二酐(BPDA)、1,2,4,5-均苯四甲酸二酐(PMDA)、4,4'-氧双邻苯二甲酸酐(ODPA)、3,3’,4,4’-二苯酮四酸二酐(BTDA)中的一种或几种组合而成。
4.根据权利要求1所述的一种石墨烧结用聚酰亚胺薄膜的制备方法,其特征在于:所述极性溶剂为二甲基乙酰胺(DMAC)、二甲基甲酰胺(DMF)或N-甲基吡咯烷酮(NMP)中的一种。
5.根据权利要求1所述的一种石墨烧结用聚酰亚胺薄膜的制备方法,其特征在于:所述导热材料为碳化硅、氮化硼、氮化铝、钙磷化合物中的一种或几种组合而成;导热材料的使用质量是树脂固体质量的0.05-8%。
6.根据权利要求1所述的一种石墨烧结用聚酰亚胺薄膜的制备方法,其特征在于:所述步骤(1)中极性溶剂的质量是二胺与二酐总质量的4-7倍。
CN201910537474.2A 2019-06-20 2019-06-20 一种石墨烧结用聚酰亚胺薄膜的制备方法 Active CN110272552B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910537474.2A CN110272552B (zh) 2019-06-20 2019-06-20 一种石墨烧结用聚酰亚胺薄膜的制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910537474.2A CN110272552B (zh) 2019-06-20 2019-06-20 一种石墨烧结用聚酰亚胺薄膜的制备方法

Publications (2)

Publication Number Publication Date
CN110272552A CN110272552A (zh) 2019-09-24
CN110272552B true CN110272552B (zh) 2021-09-17

Family

ID=67961502

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910537474.2A Active CN110272552B (zh) 2019-06-20 2019-06-20 一种石墨烧结用聚酰亚胺薄膜的制备方法

Country Status (1)

Country Link
CN (1) CN110272552B (zh)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102222571B1 (ko) * 2019-10-28 2021-03-05 피아이첨단소재 주식회사 그라파이트 시트용 폴리이미드 필름 및 이로부터 제조된 그라파이트 시트
CN113214644A (zh) * 2021-05-20 2021-08-06 广东工业大学 一种聚酰亚胺复合薄膜和石墨膜
CN113184842A (zh) * 2021-06-03 2021-07-30 中山大学 一种高石墨化石墨厚膜及其制备方法
CN113717524A (zh) * 2021-08-31 2021-11-30 安徽国风塑业股份有限公司 一种用于制备石墨膜的聚酰亚胺薄膜及其制备方法
CN114854208A (zh) * 2022-04-26 2022-08-05 苏州阳池科技有限公司 一种导热硅胶垫片复合材料及其制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6121168B2 (ja) * 2013-01-16 2017-04-26 東レ・デュポン株式会社 ポリイミドフィルム及びその製造方法
CN106853966B (zh) * 2015-12-07 2019-08-16 株洲时代新材料科技股份有限公司 利用石墨烯掺杂聚酰胺酸树脂制备高导热石墨膜的方法
CN106629699B (zh) * 2016-09-14 2018-12-07 株洲时代新材料科技股份有限公司 一种高导热石墨膜的制备方法
CN106832923B (zh) * 2016-12-16 2019-07-19 深圳瑞华泰薄膜科技股份有限公司 一种用于制备人工石墨膜的聚酰亚胺薄膜及其制备方法
KR101883434B1 (ko) * 2018-01-30 2018-07-31 에스케이씨코오롱피아이 주식회사 그라파이트 시트용 폴리이미드 필름, 이를 이용하여 제조된 그라파이트 시트 및 그라파이트 시트의 제조방법

Also Published As

Publication number Publication date
CN110272552A (zh) 2019-09-24

Similar Documents

Publication Publication Date Title
CN110272552B (zh) 一种石墨烧结用聚酰亚胺薄膜的制备方法
CN109650892B (zh) 一种高导热石墨烯膜及其制备方法
TWI649353B (zh) 聚醯亞胺膜、用其製備的石墨片材、以及石墨片材的製備方法
CN110550956A (zh) 基于石墨烯聚酰亚胺复合海绵前驱体导热薄膜的制备方法
EP2520607A2 (en) Method for manufacturing a wholly aromatic polyimide powder having an antistatic or conductive property
CN111470876B (zh) 一种高石墨化聚酰亚胺基石墨厚膜及其制备方法
CN110540752A (zh) 一种填料取向增强的高导热聚酰亚胺复合薄膜及其制备方法
CN109438735B (zh) 一种高导热聚酰亚胺基复合薄膜及其制备方法
CN106867256B (zh) 一种石墨烯织物改性各向异性导热聚酰亚胺薄膜、制备方法及应用
CN114437349B (zh) 聚酰亚胺膜、其制备方法和石墨膜
CN113717524A (zh) 一种用于制备石墨膜的聚酰亚胺薄膜及其制备方法
CN112919452A (zh) 高热通量石墨烯-聚酰亚胺碳化膜及其制备方法和用途
KR102077766B1 (ko) 그라파이트 필름, 그 제조방법 및 이를 포함하는 전자소자용 방열구조체
JP2004299919A (ja) グラファイト及びその製造方法
JPH0733875A (ja) 高結晶性ポリイミドパウダー及びその製造方法
KR102153508B1 (ko) 결정성 폴리이미드 수지 및 열전도성 필러를 포함하는 폴리이미드 필름 및 이의 제조방법
CN114516959B (zh) 聚酰胺膜、其制备方法和石墨膜
CN115216151B (zh) 一种聚酰亚胺薄膜导热通道的构建方法
CN113105657A (zh) 一种高定向、高功率石墨烯发热膜及其制备方法和用途
CN111349255B (zh) 一种石墨烯-聚酰亚胺导电膜及其制备方法
CN114479455A (zh) 一种成膜性良好的高导热聚酰亚胺薄膜及其制备方法
CN114874474A (zh) 一种耐高温高储能全有机聚酰亚胺复合薄膜及其制备方法和应用
CN108504095A (zh) 一种新型高导热导电石墨复合膜的制备方法
CN113025038B (zh) 一种含高相容性色素的黑色聚酰亚胺膜及其制备方法
CN114144390B (zh) 石墨片及包含其的电子装置

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
GR01 Patent grant
GR01 Patent grant
CP03 Change of name, title or address

Address after: 266024 room 55, No. 26, Jintan 1st Road, Shibei District, Qingdao, Shandong

Patentee after: Fuyoute (Qingdao) new material Co.,Ltd.

Address before: 201-10, block a, Chuangke street, Qingdao, No. 306, Ningxia road, Laoshan District, Qingdao, Shandong 266100

Patentee before: QINGDAO COSM NEW MATERIALS Co.,Ltd.

CP03 Change of name, title or address
TR01 Transfer of patent right

Effective date of registration: 20211124

Address after: 262500 north section of yangtianshan Road, Yidu sub district office, Qingzhou City, Weifang City, Shandong Province

Patentee after: Fuyoute (Shandong) new material technology Co.,Ltd.

Address before: 266024 room 55, No. 26, Jintan 1st Road, Shibei District, Qingdao, Shandong

Patentee before: Fuyoute (Qingdao) new material Co.,Ltd.

TR01 Transfer of patent right