CN108711467B - 一种改性复合绝缘电线及其制备方法 - Google Patents

一种改性复合绝缘电线及其制备方法 Download PDF

Info

Publication number
CN108711467B
CN108711467B CN201810397612.7A CN201810397612A CN108711467B CN 108711467 B CN108711467 B CN 108711467B CN 201810397612 A CN201810397612 A CN 201810397612A CN 108711467 B CN108711467 B CN 108711467B
Authority
CN
China
Prior art keywords
insulating layer
layer
parts
modified
weight
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
CN201810397612.7A
Other languages
English (en)
Other versions
CN108711467A (zh
Inventor
范雷方
吴振江
沈刚
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.)
Hubei Angui cable industry Co.,Ltd.
Original Assignee
Hubei Angui Cable Industry 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 Hubei Angui Cable Industry Co Ltd filed Critical Hubei Angui Cable Industry Co Ltd
Priority to CN201810397612.7A priority Critical patent/CN108711467B/zh
Publication of CN108711467A publication Critical patent/CN108711467A/zh
Application granted granted Critical
Publication of CN108711467B publication Critical patent/CN108711467B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00Insulated conductors or cables characterised by their form
    • H01B7/02Disposition of insulation
    • H01B7/0208Cables with several layers of insulating material
    • H01B7/0225Three or more layers
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4825Polyethers containing two hydroxy groups
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/6692Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/34
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/75Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
    • C08G18/751Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
    • C08G18/752Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
    • C08G18/753Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
    • C08G18/755Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
    • 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
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7614Polyisocyanates or polyisothiocyanates cyclic aromatic containing only one aromatic ring
    • 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
    • C08J9/0071Nanosized fillers, i.e. having at least one dimension below 100 nanometers
    • C08J9/008Nanoparticles
    • 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
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B13/00Apparatus or processes specially adapted for manufacturing conductors or cables
    • H01B13/06Insulating conductors or cables
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B13/00Apparatus or processes specially adapted for manufacturing conductors or cables
    • H01B13/06Insulating conductors or cables
    • H01B13/14Insulating conductors or cables by extrusion
    • H01B13/141Insulating conductors or cables by extrusion of two or more insulating layers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B13/00Apparatus or processes specially adapted for manufacturing conductors or cables
    • H01B13/06Insulating conductors or cables
    • H01B13/14Insulating conductors or cables by extrusion
    • H01B13/148Selection of the insulating material therefor
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/302Polyurethanes or polythiourethanes; Polyurea or polythiourea
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
    • H01B3/303Macromolecular 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 H01B3/38 or H01B3/302
    • H01B3/306Polyimides or polyesterimides
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00Insulated conductors or cables characterised by their form
    • H01B7/02Disposition of insulation
    • H01B7/0275Disposition of insulation comprising one or more extruded layers of insulation
    • H01B7/0283Disposition of insulation comprising one or more extruded layers of insulation comprising in addition one or more other layers of non-extruded insulation
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00Insulated conductors or cables characterised by their form
    • H01B7/02Disposition of insulation
    • H01B7/0291Disposition of insulation comprising two or more layers of insulation having different electrical properties
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00Insulated conductors or cables characterised by their form
    • H01B7/17Protection against damage caused by external factors, e.g. sheaths or armouring
    • H01B7/29Protection against damage caused by extremes of temperature or by flame
    • H01B7/292Protection against damage caused by extremes of temperature or by flame using material resistant to heat
    • 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
    • C08J2375/00Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
    • C08J2375/04Polyurethanes
    • C08J2375/08Polyurethanes from polyethers
    • 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
    • C08K2201/003Additives being defined by their diameter
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Nanotechnology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Insulating Materials (AREA)

Abstract

本发明涉及一种改性复合绝缘电线及其制造方法。根据本发明实施例的改性复合绝缘电线由金属导体、第一绝缘层、第二改性绝缘层和第三绝缘层组成。与现有技术相比,根据本发明实施例的制造方法,采用聚酰胺酰亚胺绝缘层作为第一绝缘层;采用异佛尔酮二异氰酸、聚丙二醇、四溴双酚A双2‑羟乙基醚、二月桂酸二丁基锡、偶氮二异丁腈、甲苯二异氰酸酯、二羟甲基丙酸、三乙胺、纳米氮化铝制备第二绝缘层;采用聚氨酯与聚酰亚胺复合的复合绝缘层作为第三绝缘层。由此,根据本发明实施例的改性复合绝缘电线的制造方法,可以显著提高电线的耐电压、耐电晕、耐高温、耐老化、耐冲击性能和力学性能,实现具有优异综合性能的绝缘电线,使电线应用更安全。

Description

一种改性复合绝缘电线及其制备方法
技术领域
本发明涉及一种电线及其制备方法,尤其涉及一种改性复合绝缘电线及其制备方法。
背景技术
电工装备广泛应用于各工业领域,随着科技的发展,电力、轨道交通、新能源、微电子、航空航天、国防军工等领域对于电工装备的要求不断提高。在实际应用中,电工装备不可避免地受到温度、电、机械的应力和振动,有害气体、化学物质、潮气、灰尘和辐照等各种环境因素影响,其能否持久的安全服役运行,很大程度上取决于电工设备中带有绝缘材料的元件,而电线的绝缘失效是导致电工设备故障最主要的原因。如何提高电线绝缘的电气性能、机械性能和耐环境性能,对于提高电工设备技术发展,保障电工设备在复杂环境中安全服役,具有重要意义。
发明内容
为了克服现有技术存在的不足,本发明旨在提供一种聚酰亚胺凝胶、增强聚酰亚胺双绝缘电线及其制备方法。
根据本发明的一方面,一种改性复合绝缘电线,由金属导体、第一绝缘层、第二改性绝缘层和第三绝缘层组成;所述第一绝缘层为聚酰胺酰亚胺绝缘层;所述第二绝缘层由按重量份的以下组分制成:异佛尔酮二异氰酸100重量份、聚丙二醇50-80重量份、四溴双酚A双(2-羟乙基)醚50-100重量份、二月桂酸二丁基锡2-8重量份、偶氮二异丁腈1-5重量份、甲苯二异氰酸酯1-5重量份、二羟甲基丙酸15-35重量份、三乙胺2-5重量份、纳米氮化铝0.05-3重量份;所述第三绝缘层为聚酰亚胺复合绝缘层,所述聚酰亚胺复合绝缘层由内向外依次包括内聚氨酯层、聚酰亚胺层以及外聚氨酯层。
根据本发明的另一方面,一种改性复合绝缘电线的制备方法,包括以下步骤:
在金属导体外侧包覆第一绝缘层;
将异佛尔酮二异氰酸100重量份、聚丙二醇50-80重量份、四溴双酚A双2-羟乙基醚50-100重量份、二月桂酸二丁基锡2-8重量份、偶氮二异丁腈1-5重量份、甲苯二异氰酸酯1-5重量份、二羟甲基丙酸15-35重量份、三乙胺2-5重量份、纳米氮化铝0.05-3重量份,置于反应釜中,第一反应温度为265℃-280℃、反应时间为20min-35min,第二反应温度为285℃-315℃,在第一反应与第二反应同时进行超声分散,制备改性绝缘树脂;
将改性绝缘树脂挤包在第一绝缘层外侧,挤塑温度275℃-295℃;
进行第一在线固化热处理,热处理温度为255℃-265℃,热处理速率为0.22m/s-0.65m/s;
采用三层共挤挤塑机,在第二绝缘层外侧包覆第三绝缘层,第三绝缘层由内向外依次包括内聚氨酯层、聚酰亚胺层以及外聚氨酯层,其中,内聚氨酯层与外聚氨酯层的挤塑温度为160℃-210℃,聚酰亚胺层的挤塑温度为185℃-250℃;
进行第二在线固化热处理,热处理温度为220℃-255℃,热处理速率为0.18m/s-0.75m/s,得到改性复合绝缘电线。
根据本发明的示例性实施例,所述第一绝缘层的厚度是第二绝缘层厚度的20%-35%,所述第三绝缘层的厚度是第二绝缘层厚度的80%-135%。
根据本发明的示例性实施例,所述第一绝缘层采用重叠绕包的方式包覆在金属导体上,包覆角度为35°-40°,重叠率为35%-51%。
根据本发明的示例性实施例,所述聚酰亚胺复合绝缘层由内聚氨酯层、聚酰亚胺层和外聚氨酯层组成,其中,内聚氨酯层的厚度为聚酰亚胺层厚度的50%-65%,外聚氨酯层的厚度为聚酰亚胺层厚度的70%-135%。
根据本发明的示例性实施例,所述第一绝缘层的最小体积电阻率为(200℃±2℃/1h)2.1×1015Ω·m,交流电气强度为228V/μm。
根据本发明的示例性实施例,所述第二绝缘层的厚度为10μm-800μm、相对电容率(23℃、50Hz时)2.98、介质损耗因素(23℃、50Hz时)5.28×10-3、体积电阻率(200℃±2℃/1h)1.8×1016Ω·m,表面电阻率(200℃±2℃/1h)2.2×1017Ω·m,纵向拉伸强度218MPa,纵向断裂延伸率69.9%,横向拉伸强度182MPa,横向断裂延伸率81.8%,交流电气强度365V/μm,击穿电压9.8kV。
根据本发明的示例性实施例,所述第三绝缘层的最小体积电阻率为(200℃±2℃/1h)1.8×1016Ω·m,交流电气强度为295V/μm。
根据本发明的示例性实施例,所述纳米氮化铝的粒径为25nm-80nm。
本发明的实施例综合运用材料和创新性工艺制备具有多层绝缘的电线,采用聚酰胺酰亚胺绝缘层作为第一绝缘层,采用纳米增强改性绝缘作为第二绝缘层,采用聚氨酯与聚酰亚胺复合的复合绝缘层作为第三绝缘层,显著提高电线的耐电压、耐电晕、耐高温、耐老化、耐冲击性能,实现具有优异综合性能的绝缘电线。
与现有技术相比,本发明的实施例克服了传统绝缘电线耐高温、耐电压、耐电晕性能不能同时兼具的不足,根据本发明实施例的改性复合绝缘电线,绝缘性能和力学性能优异,电线应用更安全。
具体实施方式
为使本发明技术方案和优点更加清楚,通过以下几个具体实施例对本发明作进一步详细描述。显然,所描述的实施例是本发明一部分实施例,而不是全部的实施例。基于本发明中的实施例,本领域普通技术人员在没有做出创造性劳动的前提下所获得的所有其他实施例,都属于本发明保护的范围。
实施例1
1、采用重叠绕包的方式将聚酰胺酰亚胺绝缘带包覆在金属导体上,包覆角度为35°,重叠率为51%。
2、将异佛尔酮二异氰酸100重量份、聚丙二醇50重量份、四溴双酚A双(2-羟乙基)醚55重量份、二月桂酸二丁基锡2重量份、偶氮二异丁腈1重量份、甲苯二异氰酸酯2重量份、二羟甲基丙酸16重量份、三乙胺3重量份、粒径为30nm纳米氮化铝0.08重量份,置于反应釜中,第一反应温度为265℃、反应时间为25min,第二反应温度为285℃,在第一反应与第二反应同时进行超声分散,制备改性绝缘树脂;
3、将改性绝缘树脂挤包在第一绝缘层外侧,挤塑温度275℃;
4、对步骤3中线芯进行第一在线固化热处理,热处理温度为255℃,热处理速率为0.29m/s;
5、采用三层共挤挤塑机,在第二绝缘层外侧包覆第三绝缘层,第三绝缘层由内聚氨酯层、聚酰亚胺层和外聚氨酯层组成,其中,内聚氨酯层的厚度为聚酰亚胺层厚度的50%,外聚氨酯层的厚度为聚酰亚胺层厚度的70%;其中,内聚氨酯层与外聚氨酯层的挤塑温度为165℃,聚酰亚胺层的挤塑温度为185℃;
6、对步骤5中线芯进行第二在线固化热处理,热处理温度为235℃,热处理速率为0.19m/s,得到改性复合绝缘电线。
7、制得的第一绝缘层的厚度是第二绝缘层厚度的22%,所述第三绝缘层的厚度是第二绝缘层厚度的85%。
8、制得的第一绝缘层的最小体积电阻率为(200℃±2℃/1h)2.1×1015Ω·m,交流电气强度为228V/μm。
9、制得的第二绝缘层的厚度为10μm-800μm、相对电容率(23℃、50Hz时)2.98、介质损耗因素(23℃、50Hz时)5.28×10-3、体积电阻率(200℃±2℃/1h)1.8×1016Ω·m,表面电阻率(200℃±2℃/1h)2.2×1017Ω·m,纵向拉伸强度218MPa,纵向断裂延伸率69.9%,横向拉伸强度182MPa,横向断裂延伸率81.8%,交流电气强度365V/μm,击穿电压9.8kV。
10、制得的第三绝缘层的最小体积电阻率为(200℃±2℃/1h)1.8×1016Ω·m,交流电气强度为295V/μm。
实施例2
1、采用重叠绕包的方式将聚酰胺酰亚胺绝缘带包覆在金属导体上,包覆角度为40°,重叠率为39%。
2、将异佛尔酮二异氰酸100重量份、聚丙二醇58重量份、四溴双酚A双(2-羟乙基)醚60重量份、二月桂酸二丁基锡5重量份、偶氮二异丁腈4重量份、甲苯二异氰酸酯3重量份、二羟甲基丙酸22重量份、三乙胺5重量份、粒径为50nm纳米氮化铝0.18重量份,置于反应釜中,第一反应温度为280℃、反应时间为20min,第二反应温度为295℃,在第一反应与第二反应同时进行超声分散,制备改性绝缘树脂;
3、将改性绝缘树脂挤包在第一绝缘层外侧,挤塑温度285℃;
4、对步骤3中线芯进行第一在线固化热处理,热处理温度为258℃,热处理速率为0.32m/s;
5、采用三层共挤挤塑机,在第二绝缘层外侧包覆第三绝缘层,第三绝缘层由内聚氨酯层、聚酰亚胺层和外聚氨酯层组成,其中,内聚氨酯层的厚度为聚酰亚胺层厚度的59%,外聚氨酯层的厚度为聚酰亚胺层厚度的80%;其中,内聚氨酯层与外聚氨酯层的挤塑温度为175℃,聚酰亚胺层的挤塑温度为195℃;
6、对步骤5中线芯进行第二在线固化热处理,热处理温度为235℃,热处理速率为0.55m/s,得到改性复合绝缘电线。
7、制得的第一绝缘层的厚度是第二绝缘层厚度的30%,所述第三绝缘层的厚度是第二绝缘层厚度的115%。
8、制得的第一绝缘层的最小体积电阻率为(200℃±2℃/1h)2.1×1015Ω·m,交流电气强度为228V/μm。
9、制得的第二绝缘层的厚度为10μm-800μm、相对电容率(23℃、50Hz时)2.98、介质损耗因素(23℃、50Hz时)5.28×10-3、体积电阻率(200℃±2℃/1h)1.8×1016Ω·m,表面电阻率(200℃±2℃/1h)2.2×1017Ω·m,纵向拉伸强度218MPa,纵向断裂延伸率69.9%,横向拉伸强度182MPa,横向断裂延伸率81.8%,交流电气强度365V/μm,击穿电压9.8kV。
10、制得的第三绝缘层的最小体积电阻率为(200℃±2℃/1h)1.8×1016Ω·m,交流电气强度为295V/μm。
实施例3
1、采用重叠绕包的方式将聚酰胺酰亚胺绝缘带包覆在金属导体上,包覆角度为40°,重叠率为40%。
2、将异佛尔酮二异氰酸100重量份、聚丙二醇80重量份、四溴双酚A双(2-羟乙基)醚85重量份、二月桂酸二丁基锡8重量份、偶氮二异丁腈2重量份、甲苯二异氰酸酯4重量份、二羟甲基丙酸32重量份、三乙胺4重量份、粒径为60nm纳米氮化铝1重量份,置于反应釜中,第一反应温度为280℃、反应时间为35min,第二反应温度为15℃,在第一反应与第二反应同时进行超声分散,制备改性绝缘树脂;
3、将改性绝缘树脂挤包在第一绝缘层外侧,挤塑温度295℃;
4、对步骤3中线芯进行第一在线固化热处理,热处理温度为65℃,热处理速率为0.65m/s;
5、采用三层共挤挤塑机,在第二绝缘层外侧包覆第三绝缘层,第三绝缘层由内聚氨酯层、聚酰亚胺层和外聚氨酯层组成,其中,内聚氨酯层的厚度为聚酰亚胺层厚度的65%,外聚氨酯层的厚度为聚酰亚胺层厚度的90%;其中,内聚氨酯层与外聚氨酯层的挤塑温度为190℃,聚酰亚胺层的挤塑温度为210℃;
6、对步骤5中线芯进行第二在线固化热处理,热处理温度为235℃,热处理速率为0.65m/s,得到改性复合绝缘电线。
7、制得的第一绝缘层的厚度是第二绝缘层厚度的20%,所述第三绝缘层的厚度是第二绝缘层厚度的80%。
8、制得的第一绝缘层的最小体积电阻率为(200℃±2℃/1h)2.1×1015Ω·m,交流电气强度为228V/μm。
9、制得的第二绝缘层的厚度为10μm-800μm、相对电容率(23℃、50Hz时)2.98、介质损耗因素(23℃、50Hz时)5.28×10-3、体积电阻率(200℃±2℃/1h)1.8×1016Ω·m,表面电阻率(200℃±2℃/1h)2.2×1017Ω·m,纵向拉伸强度218MPa,纵向断裂延伸率69.9%,横向拉伸强度182MPa,横向断裂延伸率81.8%,交流电气强度365V/μm,击穿电压9.8kV。
10、制得的第三绝缘层的最小体积电阻率为(200℃±2℃/1h)1.8×1016Ω·m,交流电气强度为295V/μm。
以上所述的具体实施方式,对本发明的目的、技术方案和有益效果进行了进一步详细说明,所应理解的是,以上所述仅为本发明的具体实施方式而已,并不用于限定本发明的保护范围,凡在本发明的精神和原则之内,所做的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。

Claims (8)

1.一种改性复合绝缘电线,其特征在于,所述改性复合绝缘电线由金属导体、第一绝缘层、第二改性绝缘层和第三绝缘层组成;所述第一绝缘层为聚酰胺酰亚胺绝缘层;所述第二改性绝缘层由按重量份的以下组分制成:异佛尔酮二异氰酸100重量份、聚丙二醇50-80重量份、四溴双酚A双2-羟乙基醚50-100重量份、二月桂酸二丁基锡2-8重量份、偶氮二异丁腈1-5重量份、甲苯二异氰酸酯1-5重量份、二羟甲基丙酸15-35重量份、三乙胺2-5重量份、纳米氮化铝0.05-3重量份;所述第三绝缘层为聚酰亚胺复合绝缘层,所述聚酰亚胺复合绝缘层由内向外依次包括内聚氨酯层、聚酰亚胺层以及外聚氨酯层,其中,所述第二改性绝缘层的厚度为10μm-800μm,23℃、50Hz时的相对电容率为2.98,23℃、50Hz时的介质损耗因素为5.28×10-3,200℃±2℃/1h时的体积电阻率为1.8×1016Ω·m,200℃±2℃/1h时的表面电阻率为2.2×1017Ω·m,纵向拉伸强度为218MPa,纵向断裂延伸率为69.9%,横向拉伸强度为182MPa,横向断裂延伸率为81.8%,交流电气强度为365V/μm,击穿电压为9.8kV。
2.根据权利要求1所述的改性复合绝缘电线,其特征在于,所述第一绝缘层的厚度是第二改性绝缘层厚度的20%-35%,所述第三绝缘层的厚度是第二改性绝缘层厚度的80%-135%。
3.根据权利要求1所述的改性复合绝缘电线,其特征在于,所述第一绝缘层采用重叠绕包的方式包覆在金属导体上,包覆角度为35°-40°,重叠率为35%-51%。
4.根据权利要求1所述的改性复合绝缘电线,其特征在于,内聚氨酯层的厚度为聚酰亚胺层厚度的50%-65%,外聚氨酯层的厚度为聚酰亚胺层厚度的70%-135%。
5.根据权利要求1所述的改性复合绝缘电线,其特征在于,所述第一绝缘层200℃±2℃/1h时的最小体积电阻率为2.1×1015Ω·m,交流电气强度为228V/μm。
6.根据权利要求1所述的改性复合绝缘电线,其特征在于,所述第三绝缘层200℃±2℃/1h时的最小体积电阻率为1.8×1016Ω·m,交流电气强度为295V/μm。
7.一种改性复合绝缘电线的制备方法,其特征在于,所述制备方法包括:
在金属导体外侧包覆第一绝缘层;
将异佛尔酮二异氰酸100重量份、聚丙二醇50-80重量份、四溴双酚A双2-羟乙基醚50-100重量份、二月桂酸二丁基锡2-8重量份、偶氮二异丁腈1-5重量份、甲苯二异氰酸酯1-5重量份、二羟甲基丙酸15-35重量份、三乙胺2-5重量份、纳米氮化铝0.05-3重量份,置于反应釜中,第一反应温度为265℃-280℃、反应时间为20min-35min,第二反应温度为285℃-315℃,在第一反应与第二反应同时进行超声分散,制备改性绝缘树脂;
将改性绝缘树脂挤包在第一绝缘层外侧,挤塑温度275℃-295℃;
进行第一在线固化热处理,热处理温度为255℃-265℃,热处理速率为0.22m/s-0.65m/s;
采用三层共挤挤塑机,在第二改性绝缘层外侧包覆第三绝缘层,第三绝缘层由内向外依次包括内聚氨酯层、聚酰亚胺层以及外聚氨酯层,其中,内聚氨酯层与外聚氨酯层的挤塑温度为160℃-210℃,聚酰亚胺层的挤塑温度为185℃-250℃;
进行第二在线固化热处理,热处理温度为220℃-255℃,热处理速率为0.18m/s-0.75m/s,得到改性复合绝缘电线。
8.根据权利要求7所述的制备方法,其特征在于,所述纳米氮化铝的粒径为25nm-80nm。
CN201810397612.7A 2018-04-28 2018-04-28 一种改性复合绝缘电线及其制备方法 Active CN108711467B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810397612.7A CN108711467B (zh) 2018-04-28 2018-04-28 一种改性复合绝缘电线及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810397612.7A CN108711467B (zh) 2018-04-28 2018-04-28 一种改性复合绝缘电线及其制备方法

Publications (2)

Publication Number Publication Date
CN108711467A CN108711467A (zh) 2018-10-26
CN108711467B true CN108711467B (zh) 2020-06-30

Family

ID=63867647

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810397612.7A Active CN108711467B (zh) 2018-04-28 2018-04-28 一种改性复合绝缘电线及其制备方法

Country Status (1)

Country Link
CN (1) CN108711467B (zh)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6214462B1 (en) * 1990-02-16 2001-04-10 Alcatel N.V. Enameling lacquer, process for the manufacture of the lacquer and application of the lacquer to enameling wires
CN101824268A (zh) * 2010-05-07 2010-09-08 江苏八达线缆有限公司 一种漆包线用纳米复合改性绝缘油漆的制备方法及高性能纳米复合漆包线
CN107141624A (zh) * 2017-06-06 2017-09-08 合肥市闵葵电力工程有限公司 一种电缆用导热阻燃耐候防静电环保绝缘材料及其制备方法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6214462B1 (en) * 1990-02-16 2001-04-10 Alcatel N.V. Enameling lacquer, process for the manufacture of the lacquer and application of the lacquer to enameling wires
CN101824268A (zh) * 2010-05-07 2010-09-08 江苏八达线缆有限公司 一种漆包线用纳米复合改性绝缘油漆的制备方法及高性能纳米复合漆包线
CN107141624A (zh) * 2017-06-06 2017-09-08 合肥市闵葵电力工程有限公司 一种电缆用导热阻燃耐候防静电环保绝缘材料及其制备方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
"阻燃型聚氨酯材料的制备";高丽君等;《工程塑料应用》;20180131;第46卷(第1期);第106-108页 *

Also Published As

Publication number Publication date
CN108711467A (zh) 2018-10-26

Similar Documents

Publication Publication Date Title
US8847075B2 (en) Insulated wire
US9324476B2 (en) Insulated winding wire
KR102005113B1 (ko) 절연 조성물 및 이를 포함하는 전기 케이블
WO2015130681A1 (en) Insulated winding wire
EP3134906B1 (en) Continuously transposed conductor
CN101436449B (zh) 能抑制绝缘层内部电树枝生成与发展的高压、超高压电缆
EP3014630B1 (en) A material comprising reduced graphene oxide, a device comprising the material and a method of producing the material
US20110232937A1 (en) Conductive elastomer and method of applying a conductive coating to a cable
US11045998B2 (en) Producing power bushing condenser core by additive manufacturing
US10199138B2 (en) Insulated winding wire
CN108711467B (zh) 一种改性复合绝缘电线及其制备方法
KR100928661B1 (ko) 자기융착 및 난연성 실리콘 절연테이프의 제조방법 및 자기융착 및 난연성 실리콘 절연테이프
KR20070027583A (ko) 운모 함량이 최대화된 마이카 테이프
US20150279510A1 (en) Winding Wire and Composition for Wiring Wire
JP6740642B2 (ja) 絶縁電線の製造方法
Megala et al. Application of PI/MWCNT nanocomposite for AC corona discharge reduction
CN108610629A (zh) 一种改性增强耐电晕电线及其制备方法
US20150243409A1 (en) Insulated winding wire containing semi-conductive layers
Van Nguyen et al. AC breakdown channel of PPLP multi-layer insulation for HTS cable
US20180322980A1 (en) Surface Treating Magnet Wire Enamel Layers To Promote Layer Adhesion
CN217606579U (zh) 异型绝缘电线、线圈和电子/电气设备
KR102186584B1 (ko) 가공 케이블용 구리-마일라 테이프 및 그 제조 방법
Hwang et al. Surface breakdown characteristics of composite insulating papers in LN 2 for a stop joint box of dc HTS power cable
Park et al. Effect of Conductor Radius of Polyesterimide-Polyamideimide Enameled Round Wire on Insulation Breakdown Voltage and Insulation Lifetime
Park et al. Effect of Winding Coil Diameter on AC Insulation Breakdown Voltage of Polyamideimide/Nanosilica Wire

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

Effective date of registration: 20200604

Address after: Datong group, yangqueba village, wuyangba sub district office, Enshi City, Enshi Tujia and Miao Autonomous Prefecture, Hubei Province, 445000

Applicant after: Hubei Angui cable industry Co.,Ltd.

Address before: 201100 No. 2099, friendship road, Shanghai, Minhang District

Applicant before: CHUANYE ELECTRONIC TECHNOLOGY (SHANGHAI) Co.,Ltd.

TA01 Transfer of patent application right
GR01 Patent grant
GR01 Patent grant
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: A modified composite insulated wire and its preparation method

Effective date of registration: 20230407

Granted publication date: 20200630

Pledgee: Enshi Branch of Bank of China Ltd.

Pledgor: Hubei Angui cable industry Co.,Ltd.

Registration number: Y2023980037526

PE01 Entry into force of the registration of the contract for pledge of patent right