CN107043535A - 一种铋、锰、钴、铌掺杂的氧化锌‑聚酰亚胺复合薄膜及其制备方法 - Google Patents
一种铋、锰、钴、铌掺杂的氧化锌‑聚酰亚胺复合薄膜及其制备方法 Download PDFInfo
- Publication number
- CN107043535A CN107043535A CN201710276307.8A CN201710276307A CN107043535A CN 107043535 A CN107043535 A CN 107043535A CN 201710276307 A CN201710276307 A CN 201710276307A CN 107043535 A CN107043535 A CN 107043535A
- Authority
- CN
- China
- Prior art keywords
- parts
- zinc oxide
- bismuth
- manganese
- cobalt
- 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
Links
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 title claims abstract description 44
- 239000004642 Polyimide Substances 0.000 title claims abstract description 30
- 229920001721 polyimide Polymers 0.000 title claims abstract description 30
- 229910052797 bismuth Inorganic materials 0.000 title claims abstract description 28
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 229910017052 cobalt Inorganic materials 0.000 title claims abstract description 28
- 239000010941 cobalt Substances 0.000 title claims abstract description 28
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 title claims abstract description 28
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 title claims abstract description 28
- 229910052758 niobium Inorganic materials 0.000 title claims abstract description 28
- 239000010955 niobium Substances 0.000 title claims abstract description 28
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 239000002131 composite material Substances 0.000 title claims abstract description 26
- 239000011787 zinc oxide Substances 0.000 title claims abstract description 15
- 238000002360 preparation method Methods 0.000 title description 5
- 238000006243 chemical reaction Methods 0.000 claims abstract description 28
- 239000002245 particle Substances 0.000 claims abstract description 14
- 229960001296 zinc oxide Drugs 0.000 claims abstract description 14
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 claims abstract description 10
- 230000008859 change Effects 0.000 claims abstract description 5
- 238000005266 casting Methods 0.000 claims abstract description 4
- 238000011065 in-situ storage Methods 0.000 claims abstract description 4
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 28
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 27
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 20
- 229910052725 zinc Inorganic materials 0.000 claims description 19
- 239000011701 zinc Substances 0.000 claims description 19
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 claims description 12
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 12
- 239000000243 solution Substances 0.000 claims description 12
- 238000003756 stirring Methods 0.000 claims description 12
- UBEWDCMIDFGDOO-UHFFFAOYSA-N cobalt(2+);cobalt(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Co+2].[Co+3].[Co+3] UBEWDCMIDFGDOO-UHFFFAOYSA-N 0.000 claims description 10
- 239000000843 powder Substances 0.000 claims description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 9
- 239000000047 product Substances 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 claims description 6
- 229910000416 bismuth oxide Inorganic materials 0.000 claims description 6
- 238000001354 calcination Methods 0.000 claims description 6
- 239000008367 deionised water Substances 0.000 claims description 6
- 229910021641 deionized water Inorganic materials 0.000 claims description 6
- TYIXMATWDRGMPF-UHFFFAOYSA-N dibismuth;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Bi+3].[Bi+3] TYIXMATWDRGMPF-UHFFFAOYSA-N 0.000 claims description 6
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 6
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 6
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 5
- HQROXDLWVGFPDE-UHFFFAOYSA-N 1-chloro-4-nitro-2-(trifluoromethyl)benzene Chemical class [O-][N+](=O)C1=CC=C(Cl)C(C(F)(F)F)=C1 HQROXDLWVGFPDE-UHFFFAOYSA-N 0.000 claims description 4
- 238000010907 mechanical stirring Methods 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 238000000498 ball milling Methods 0.000 claims description 3
- 230000006837 decompression Effects 0.000 claims description 3
- -1 dimethyl diphenyl methane diamines Chemical class 0.000 claims description 3
- 238000007599 discharging Methods 0.000 claims description 3
- 239000000706 filtrate Substances 0.000 claims description 3
- 239000005357 flat glass Substances 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000005457 ice water Substances 0.000 claims description 3
- 239000011259 mixed solution Substances 0.000 claims description 3
- 239000000376 reactant Substances 0.000 claims description 3
- 238000007493 shaping process Methods 0.000 claims description 3
- 238000007873 sieving Methods 0.000 claims description 3
- 239000002002 slurry Substances 0.000 claims description 3
- 239000007921 spray Substances 0.000 claims description 3
- 239000000725 suspension Substances 0.000 claims description 3
- 238000010792 warming Methods 0.000 claims description 3
- 238000013019 agitation Methods 0.000 claims description 2
- 150000004985 diamines Chemical class 0.000 claims description 2
- 150000002466 imines Chemical class 0.000 claims description 2
- YTVNOVQHSGMMOV-UHFFFAOYSA-N naphthalenetetracarboxylic dianhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=C2C(=O)OC(=O)C1=C32 YTVNOVQHSGMMOV-UHFFFAOYSA-N 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims 1
- 230000005684 electric field Effects 0.000 abstract description 14
- 230000003044 adaptive effect Effects 0.000 abstract description 2
- 229920003223 poly(pyromellitimide-1,4-diphenyl ether) Polymers 0.000 abstract description 2
- BFCFYVKQTRLZHA-UHFFFAOYSA-N 1-chloro-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1Cl BFCFYVKQTRLZHA-UHFFFAOYSA-N 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
- 238000009826 distribution Methods 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 239000012212 insulator Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910021521 yttrium barium copper oxide Inorganic materials 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920002379 silicone rubber Polymers 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 230000001131 transforming effect Effects 0.000 description 2
- OXHNLMTVIGZXSG-UHFFFAOYSA-N 1-Methylpyrrole Chemical class CN1C=CC=C1 OXHNLMTVIGZXSG-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- NSMZCUAVEOTJDS-UHFFFAOYSA-N 4-chloro-2-methyl-1-nitrobenzene Chemical class CC1=CC(Cl)=CC=C1[N+]([O-])=O NSMZCUAVEOTJDS-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000002322 conducting polymer Substances 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000006159 dianhydride group Chemical group 0.000 description 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular 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
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/1039—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors comprising halogen-containing substituents
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
- C08K3/36—Silica
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2379/00—Characterised 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
- C08J2379/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C08J2379/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2227—Oxides; Hydroxides of metals of aluminium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2262—Oxides; Hydroxides of metals of manganese
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2289—Oxides; Hydroxides of metals of cobalt
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2296—Oxides; Hydroxides of metals of zinc
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/16—Applications used for films
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)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
Abstract
一种铋、锰、钴、铌掺杂的氧化锌‑聚酰亚胺复合薄膜,其特征在于,首先以铋、锰、钴、铌掺杂氧化锌得到非线性介电特性的氧化锌粉体颗粒;再以对苯二酚和3‑三氟甲基‑4‑氯硝基苯反应得到含氟化合物;在氧化锌粉体颗粒表面原位聚合聚酰亚胺,并以含氟化合物改性,赋予氧化锌粉体颗粒非线性电导特性;最后流延成膜和程序升温亚胺化,得到一种铋、锰、钴、铌掺杂的氧化锌‑聚酰亚胺复合薄膜。本发明的复合薄膜,不仅同时具有非线性电导特性和非线性介电特性,可以随外加电场而自适应变化,有助于电场分布不均匀的问题;而且其强度、刚性、透明度、和尺寸稳定性均较现有聚酰亚胺薄膜有了显著提高。
Description
技术领域
本发明属于材料领域,具体涉及一种铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜及其制备方法。
背景技术
在高压、超高压乃至特高压交直流输变电系统(简称为高压输变电系统)中,系统电压等级越高,绝缘问题的重要性和困难度均越加显著。高压输变电系统中的绝缘设备或部件,其自身所承受的电场分布往往极不均匀,例如电缆终端的绝缘部分、各种绝缘子的高压端部分等,所承受的电场强度远远超出整体电场强度的平均值,甚至达到平均值的数倍,由此带来了一系列设计、制造方面的不利影响。因此,合理改善绝缘设备或部件整体电场分布的均匀程度,缓和局部的高电场强度,可以降低高压(特别是特高压)设备设计、制造的技术难度,降低电力设备造价,并提高设备长期运行的安全可靠性。
改善电场分布的传统方法主要包括:通过改变电极形状、在绝缘介质内嵌入金属起到内屏蔽作用、在绝缘介质内部加多层平行电容极板、在绝缘介质表面或外围布置均压环作为中间电极、安装并联均压电容等改善绝缘设备或部件整体电场分布均匀程度。这些法主要从电极的几何结构与分布的优化这一方面入手改善电场分布,但其对设备前期设计以及生产制造的要求很高,增加了物料与生产过程中的成本,并且均匀场强的实际效果也十分有限。但如果能够从绝缘材料自身的介电特性入手使其具备均匀场强的功能,则能够克服上述问题并且达到更理想的均匀场强的效果。
作者谢竟成等人在《超导YBa2Cu3O7+δ/硅橡胶复合材料的压敏与介电特性》一文中,采用YBa2Cu3O7+δ(简称YBCO)多晶陶瓷超导粉末与硅橡胶按不同质量比进行配料,经过特殊的制备工艺,合成不同含量的超导YBCO/硅橡胶高分子复合材料。结果表明,该复合材料在不同应力作用下,电阻值的变化范围在1-4个数量级,但是无法改善电场分布不均的问题。
发明内容
本发明的目的在于提供一种电导和介电非线性分布的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜及其制备方法。
为了实现上述目的,本发明采用了如下技术方案:
一种铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其特征在于,首先以铋、锰、钴、铌掺杂氧化锌得到非线性介电特性的氧化锌粉体颗粒;再以对苯二酚和3-三氟甲基-4-氯硝基苯反应得到含氟化合物;在氧化锌粉体颗粒表面原位聚合聚酰亚胺,并以含氟化合物改性,赋予氧化锌粉体颗粒非线性电导特性;最后流延成膜和程序升温亚胺化,得到一种铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜。
所述的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其特征在于,其由如下重量份的原料制备而成:氧化锌20-25份、氧化铋0.5-1份、二氧化锰2-3份、四氧化三钴0.6-0.8份、五氧化二铌0.5-0.7份、二氧化硅3-4份、氧化铝10-12份、对苯二酚15-20份、3-三氟甲基-4-氯硝基苯12-15份、无水碳酸钾3-4份、DMF40-50份、甲苯100-120份、丙酮40-50份、无水乙醇150-200份、盐酸溶液80-100份、氢氧化钠8-10份、N-甲基吡咯烷酮180-200份、三氟乙酞丙酮25-30份、二甲基二苯甲烷二胺350-400份、4,4′-二氨基二苯醚150-200份、1,4,5,8-萘四甲酸二酐200-220份、去离子水适量。
所述的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其特征在于,其由如下步骤制备而成:
(1)将氧化锌、氧化铋、二氧化锰、四氧化三钴、五氧化二铌、二氧化硅和氧化铝湿法球磨混合均匀,将混合好的溶浆通过喷雾造粒机喷雾成型,并对所得粉料过120-150目筛;将过筛后的粉料置于管式炉中煅烧,以20-30℃/min的速率升温至1300-1400℃,并恒温煅烧5-6h,并冷却至室温;将煅烧后的粉料碾碎,球磨,过220-250目筛,得到非线性介电特性的氧化锌粉体颗粒;
(2)在反应容器中,加入对苯二酚、3-三氟甲基-4-氯硝基苯和无水碳酸钾,搅拌均匀后再加入DMF和甲苯,通入氮气,在机械搅拌下,110-120℃反应5-6h;升温蒸出反应体系内的甲苯,150-160℃继续搅拌反应6-8h,出料,将反应液倒入冷水中,过滤并用去离子水洗涤2-3次;将所得固体加入到丙酮、1/3无水乙醇和与丙酮相同重量份的去离子水中,在机械搅拌下,加热至回流,向反应体系中缓慢滴入盐酸溶液,滴加完毕后反应物继续回流5-6h,加入氢氧化钠,搅拌5-8min后趁热过滤,将所得滤液减压蒸馏蒸出溶剂后,用剩余的无水乙醇的混合溶液重结晶,80-100℃烘箱中空气干燥10-12h,得到含氟化合物;
(3)将反应容器置于冰水浴中,将步骤(1)的产物、步骤(2)的产物置于反应容器中,加入N-甲基吡咯烷酮,超声震荡50-60min,形成稳定的悬浮液,通氮气,加入三氟乙酞丙酮、二甲基二苯甲烷二胺和4,4′-二氨基二苯醚,剧烈搅拌2-3h,分三次,每隔0.5h,加入1,4,5,8-萘四甲酸二酐,加完后继续搅拌5-6h;
(4)将步骤(3)的产物趁热在平板玻璃上涂膜,在60-70℃烘干溶剂,然后梯度升温亚胺化:150、200、250、300、350℃/30min,得到铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜。
所述的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其特征在于,所述的盐酸溶液的浓度为0.2-0.3mol/L。
采用上述的技术方案,本发明的有益效果为:
本发明以铋、锰、钴、铌掺杂氧化锌得到非线性介电特性的氧化锌粉体颗粒,铋、锰、钴、铌掺杂氧化锌使得氧化锌晶粒之间形成了具有非线性压敏电导和介电特性的晶界,使得氧化锌粉体颗粒整体具备良好的非线性介电性能。本发明以对苯二酚和3-三氟甲基-4-氯硝基苯反应得到含氟化合物,再以此含氟化合物改性聚酰亚胺,往聚酰亚胺上引入含氟侧基,降低分子链间的相互作用力,但不破坏分子链的刚性,可以在保证聚酰亚胺热稳定性的同时,改善聚酰亚胺的加工性能,提高其溶解性。本发明再在氧化锌粉体颗粒表面,原位聚合非线性导电聚合物聚酰亚胺,最后流延成膜和程序升温亚胺化,得到一种铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜;本发明的复合薄膜,不仅同时具有非线性电导特性和非线性介电特性,可以随外加电场而自适应变化,有助于更有效、广泛地解决高电压等级电力系统绝缘设备或部件电场分布不均匀的难题;对于交流系统中,由外加电压导致的不均匀电场,能以非线性介电特性为主导因素改善电场分布,同时复合材料具有的非线性电导特性也能消散积累的空间电荷,避免因其导致的局部电场集中。对于直流系统,在正常工况下由复合材料的非线性电导特性主导改善外部电压以及空间电荷导致的不均匀电场,在各种暂态电场作用下则可以发挥非线性介电特性的作用。本发明的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其强度、刚性、透明度、和尺寸稳定性均较现有聚酰亚胺薄膜有了显著提高。
具体实施方式
本实施例的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其由如下重量份的原料制备而成:氧化锌25份、氧化铋1份、二氧化锰3份、四氧化三钴0.8份、五氧化二铌0.7份、二氧化硅4份、氧化铝12份、对苯二酚20份、3-三氟甲基-4-氯硝基苯15份、无水碳酸钾4份、DMF50份、甲苯120份、丙酮50份、无水乙醇200份、盐酸溶液100份、氢氧化钠10份、N-甲基吡咯烷酮200份、三氟乙酞丙酮30份、二甲基二苯甲烷二胺400份、4,4′-二氨基二苯醚200份、1,4,5,8-萘四甲酸二酐220份、去离子水适量。
本实施例的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其由如下步骤制备而成:
(1)将氧化锌、氧化铋、二氧化锰、四氧化三钴、五氧化二铌、二氧化硅和氧化铝湿法球磨混合均匀,将混合好的溶浆通过喷雾造粒机喷雾成型,并对所得粉料过150目筛;将过筛后的粉料置于管式炉中煅烧,以30℃/min的速率升温至1400℃,并恒温煅烧6h,并冷却至室温;将煅烧后的粉料碾碎,球磨,过250目筛,得到非线性介电特性的氧化锌粉体颗粒;
(2)在反应容器中,加入对苯二酚、3-三氟甲基-4-氯硝基苯和无水碳酸钾,搅拌均匀后再加入DMF和甲苯,通入氮气,在机械搅拌下,120℃反应6h;升温蒸出反应体系内的甲苯,160℃继续搅拌反应8h,出料,将反应液倒入冷水中,过滤并用去离子水洗涤3次;将所得固体加入到丙酮、1/3无水乙醇和与丙酮相同重量份的去离子水中,在机械搅拌下,加热至回流,向反应体系中缓慢滴入盐酸溶液,滴加完毕后反应物继续回流6h,加入氢氧化钠,搅拌8min后趁热过滤,将所得滤液减压蒸馏蒸出溶剂后,用剩余的无水乙醇的混合溶液重结晶,100℃烘箱中空气干燥12h,得到含氟化合物;
(3)将反应容器置于冰水浴中,将步骤(1)的产物、步骤(2)的产物置于反应容器中,加入N-甲基吡咯烷酮,超声震荡60min,形成稳定的悬浮液,通氮气,加入三氟乙酞丙酮、二甲基二苯甲烷二胺和4,4′-二氨基二苯醚,剧烈搅拌3h,分三次,每隔0.5h,加入1,4,5,8-萘四甲酸二酐,加完后继续搅拌6h;
(4)将步骤(3)的产物趁热在平板玻璃上涂膜,在70℃烘干溶剂,然后梯度升温亚胺化:150、200、250、300、350℃/30min,得到铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜。
本实施例的盐酸溶液的浓度为0.3mol/L。
Claims (4)
1.一种铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其特征在于,首先以铋、锰、钴、铌掺杂氧化锌得到非线性介电特性的氧化锌粉体颗粒;再以对苯二酚和3-三氟甲基-4-氯硝基苯反应得到含氟化合物;在氧化锌粉体颗粒表面原位聚合聚酰亚胺,并以含氟化合物改性,赋予氧化锌粉体颗粒非线性电导特性;最后流延成膜和程序升温亚胺化,得到一种铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜。
2.根据权利要求书1所述的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其特征在于,其由如下重量份的原料制备而成:氧化锌20-25份、氧化铋0.5-1份、二氧化锰2-3份、四氧化三钴0.6-0.8份、五氧化二铌0.5-0.7份、二氧化硅3-4份、氧化铝10-12份、对苯二酚15-20份、3-三氟甲基-4-氯硝基苯12-15份、无水碳酸钾3-4份、DMF40-50份、甲苯100-120份、丙酮40-50份、无水乙醇150-200份、盐酸溶液80-100份、氢氧化钠8-10份、N-甲基吡咯烷酮180-200份、三氟乙酞丙酮25-30份、二甲基二苯甲烷二胺350-400份、4,4′-二氨基二苯醚150-200份、1,4,5,8-萘四甲酸二酐200-220份、去离子水适量。
3.根据权利要求书1所述的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其特征在于,其由如下步骤制备而成:
(1)将氧化锌、氧化铋、二氧化锰、四氧化三钴、五氧化二铌、二氧化硅和氧化铝湿法球磨混合均匀,将混合好的溶浆通过喷雾造粒机喷雾成型,并对所得粉料过120-150目筛;将过筛后的粉料置于管式炉中煅烧,以20-30℃/min的速率升温至1300-1400℃,并恒温煅烧5-6h,并冷却至室温;将煅烧后的粉料碾碎,球磨,过220-250目筛,得到非线性介电特性的氧化锌粉体颗粒;
(2)在反应容器中,加入对苯二酚、3-三氟甲基-4-氯硝基苯和无水碳酸钾,搅拌均匀后再加入DMF和甲苯,通入氮气,在机械搅拌下,110-120℃反应5-6h;升温蒸出反应体系内的甲苯,150-160℃继续搅拌反应6-8h,出料,将反应液倒入冷水中,过滤并用去离子水洗涤2-3次;将所得固体加入到丙酮、1/3无水乙醇和与丙酮相同重量份的去离子水中,在机械搅拌下,加热至回流,向反应体系中缓慢滴入盐酸溶液,滴加完毕后反应物继续回流5-6h,加入氢氧化钠,搅拌5-8min后趁热过滤,将所得滤液减压蒸馏蒸出溶剂后,用剩余的无水乙醇的混合溶液重结晶,80-100℃烘箱中空气干燥10-12h,得到含氟化合物;
(3)将反应容器置于冰水浴中,将步骤(1)的产物、步骤(2)的产物置于反应容器中,加入N-甲基吡咯烷酮,超声震荡50-60min,形成稳定的悬浮液,通氮气,加入三氟乙酞丙酮、二甲基二苯甲烷二胺和4,4′-二氨基二苯醚,剧烈搅拌2-3h,分三次,每隔0.5h,加入1,4,5,8-萘四甲酸二酐,加完后继续搅拌5-6h;
(4)将步骤(3)的产物趁热在平板玻璃上涂膜,在60-70℃烘干溶剂,然后梯度升温亚胺化:150、200、250、300、350℃/30min,得到铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜。
4.根据权利要求书2、3所述的铋、锰、钴、铌掺杂的氧化锌-聚酰亚胺复合薄膜,其特征在于,所述的盐酸溶液的浓度为0.2-0.3mol/L。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710276307.8A CN107043535A (zh) | 2017-04-25 | 2017-04-25 | 一种铋、锰、钴、铌掺杂的氧化锌‑聚酰亚胺复合薄膜及其制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710276307.8A CN107043535A (zh) | 2017-04-25 | 2017-04-25 | 一种铋、锰、钴、铌掺杂的氧化锌‑聚酰亚胺复合薄膜及其制备方法 |
Publications (1)
Publication Number | Publication Date |
---|---|
CN107043535A true CN107043535A (zh) | 2017-08-15 |
Family
ID=59545793
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710276307.8A Pending CN107043535A (zh) | 2017-04-25 | 2017-04-25 | 一种铋、锰、钴、铌掺杂的氧化锌‑聚酰亚胺复合薄膜及其制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN107043535A (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110643041A (zh) * | 2019-10-23 | 2020-01-03 | 合肥中汇睿能能源科技有限公司 | 一种折射率可调控的无色透明聚酰亚胺薄膜及其制备方法 |
CN113402883A (zh) * | 2021-07-20 | 2021-09-17 | 江苏传艺科技股份有限公司 | 一种高导热聚酰亚胺薄膜及其生产工艺 |
CN114854061A (zh) * | 2022-05-25 | 2022-08-05 | 哈尔滨理工大学 | 一种施主掺杂二氧化硅/聚酰亚胺基复合薄膜的制备方法及应用 |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1147679A (zh) * | 1995-09-07 | 1997-04-16 | 三菱电机株式会社 | 电压非线性电阻及其制造方法 |
CN1361097A (zh) * | 2000-12-27 | 2002-07-31 | 中国科学院化学研究所 | 一种含氟有机二胺及其衍生物和它们的制备方法及用途 |
CN1801409A (zh) * | 2005-11-16 | 2006-07-12 | 华东师范大学 | 一种低温烧结制备高电位梯度氧化锌压敏电阻材料的方法 |
CN1821215A (zh) * | 2006-03-23 | 2006-08-23 | 兰州大学 | 含氟不对称芳香性醚二胺及其制备和应用 |
CN101085744A (zh) * | 2007-07-11 | 2007-12-12 | 吉林大学 | 含氟芳香二胺基单体及其合成方法 |
CN101157551A (zh) * | 2007-09-12 | 2008-04-09 | 山东中厦电子科技有限公司 | 一种低压/高α值的ZnO压敏元件及其制造方法 |
CN101627448A (zh) * | 2007-03-05 | 2010-01-13 | 株式会社东芝 | ZnO非线性电阻粉末 |
CN102391646A (zh) * | 2011-11-07 | 2012-03-28 | 西安交通大学 | 一种增强型高绝缘复合材料及其制备方法 |
CN102424576A (zh) * | 2011-08-31 | 2012-04-25 | 清华大学 | 具有自适应均匀电场作用的非线性复合材料的制备方法 |
CN103172859A (zh) * | 2013-04-16 | 2013-06-26 | 株洲时代电气绝缘有限责任公司 | 聚酰胺酸分散液及其制备方法和聚酰亚胺薄膜 |
CN105153699A (zh) * | 2015-07-31 | 2015-12-16 | 江苏省电力公司泰州供电公司 | 一种超支化共聚聚酰亚胺/氧化锌杂化绝缘薄膜的制备方法 |
-
2017
- 2017-04-25 CN CN201710276307.8A patent/CN107043535A/zh active Pending
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1147679A (zh) * | 1995-09-07 | 1997-04-16 | 三菱电机株式会社 | 电压非线性电阻及其制造方法 |
CN1361097A (zh) * | 2000-12-27 | 2002-07-31 | 中国科学院化学研究所 | 一种含氟有机二胺及其衍生物和它们的制备方法及用途 |
CN1801409A (zh) * | 2005-11-16 | 2006-07-12 | 华东师范大学 | 一种低温烧结制备高电位梯度氧化锌压敏电阻材料的方法 |
CN1821215A (zh) * | 2006-03-23 | 2006-08-23 | 兰州大学 | 含氟不对称芳香性醚二胺及其制备和应用 |
CN101627448A (zh) * | 2007-03-05 | 2010-01-13 | 株式会社东芝 | ZnO非线性电阻粉末 |
CN101085744A (zh) * | 2007-07-11 | 2007-12-12 | 吉林大学 | 含氟芳香二胺基单体及其合成方法 |
CN101157551A (zh) * | 2007-09-12 | 2008-04-09 | 山东中厦电子科技有限公司 | 一种低压/高α值的ZnO压敏元件及其制造方法 |
CN102424576A (zh) * | 2011-08-31 | 2012-04-25 | 清华大学 | 具有自适应均匀电场作用的非线性复合材料的制备方法 |
CN102391646A (zh) * | 2011-11-07 | 2012-03-28 | 西安交通大学 | 一种增强型高绝缘复合材料及其制备方法 |
CN103172859A (zh) * | 2013-04-16 | 2013-06-26 | 株洲时代电气绝缘有限责任公司 | 聚酰胺酸分散液及其制备方法和聚酰亚胺薄膜 |
CN105153699A (zh) * | 2015-07-31 | 2015-12-16 | 江苏省电力公司泰州供电公司 | 一种超支化共聚聚酰亚胺/氧化锌杂化绝缘薄膜的制备方法 |
Non-Patent Citations (2)
Title |
---|
藏雨: "《气体分离膜材料科学》", 31 January 2017, 哈尔滨工业大学出版社 * |
马鸿飞: "《有机化学及单元反应》", 30 November 1997, 中国矿业大学大学出版社 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110643041A (zh) * | 2019-10-23 | 2020-01-03 | 合肥中汇睿能能源科技有限公司 | 一种折射率可调控的无色透明聚酰亚胺薄膜及其制备方法 |
CN113402883A (zh) * | 2021-07-20 | 2021-09-17 | 江苏传艺科技股份有限公司 | 一种高导热聚酰亚胺薄膜及其生产工艺 |
CN113402883B (zh) * | 2021-07-20 | 2022-03-15 | 江苏传艺科技股份有限公司 | 一种高导热聚酰亚胺薄膜及其生产工艺 |
CN114854061A (zh) * | 2022-05-25 | 2022-08-05 | 哈尔滨理工大学 | 一种施主掺杂二氧化硅/聚酰亚胺基复合薄膜的制备方法及应用 |
CN114854061B (zh) * | 2022-05-25 | 2022-09-30 | 哈尔滨理工大学 | 一种施主掺杂二氧化硅/聚酰亚胺基复合薄膜的制备方法及应用 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107043535A (zh) | 一种铋、锰、钴、铌掺杂的氧化锌‑聚酰亚胺复合薄膜及其制备方法 | |
KR101831009B1 (ko) | 폴리이미드 전구체 수용액 조성물, 및 폴리이미드 전구체 수용액 조성물의 제조 방법 | |
CN105330860B (zh) | 热塑性聚酰亚胺树脂粉及其制备方法 | |
CN103965770B (zh) | 耐高温聚酰亚胺漆包线漆及其制备方法 | |
CN109438703B (zh) | 黑色聚酰亚胺微球及其制备方法及含其薄膜的制备方法 | |
CN110092929A (zh) | 聚酰亚胺膜、用其制备的石墨片材、石墨片材的制备方法 | |
CN105237785A (zh) | 一种聚酰亚胺薄膜的制备方法 | |
CN106432724B (zh) | 一种黑色亚光聚酰亚胺薄膜及其制备方法 | |
CN110304625A (zh) | 石墨烯诱导聚酰亚胺取向晶化的高导热石墨膜的制备方法 | |
CN102120820B (zh) | 一种水相合成热固性聚酰亚胺的方法 | |
CN102363710A (zh) | 一种耐高温聚酰亚胺漆包线漆液及其制备和应用 | |
CN103922989B (zh) | 含邻苯二甲腈结构的吡咯基芳香二胺及其制备方法和应用 | |
CN115260491B (zh) | 一种耐碱解型聚酰亚胺工程塑料及其制备方法 | |
CN101392056A (zh) | 高性能低成本聚酰亚胺预聚物及其制备方法 | |
JP2023004893A (ja) | アントラキノン誘導体テトラアミンモノマー、それに由来する真性黒色ポリイミド及びその調製方法 | |
CN104231269A (zh) | 一种聚酰亚胺及其制备方法和聚酰亚胺模塑粉 | |
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 | |
CN107123463B (zh) | 一种可自适应调控电导及介电的氧化锌复合绝缘材料及其制备方法 | |
CN107099093A (zh) | 一种应用于电缆终端结构的聚丙烯‑三元乙丙橡胶护套管复合材料及其制备方法 | |
CN110358121B (zh) | 一种通过微波辐射低温制备聚酰亚胺薄膜的方法 | |
CN112940254A (zh) | 一种用于微胶囊型固化剂的聚酰亚胺外壳及其制备方法 | |
CN103408521B (zh) | 一种聚合级4,4’-对苯二甲酰二邻苯二甲酸酐的制法及其产品和用途 | |
CN104974362B (zh) | 一种聚酰亚胺薄膜的制备工艺 | |
CN110437614A (zh) | 可成型聚酰亚胺薄膜的制备方法 | |
KR101259544B1 (ko) | 폴리이미드 필름 |
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 | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20170815 |
|
RJ01 | Rejection of invention patent application after publication |