CN105885767A - Mdi基聚氨酯电子灌封胶与其制备方法和应用方法 - Google Patents

Mdi基聚氨酯电子灌封胶与其制备方法和应用方法 Download PDF

Info

Publication number
CN105885767A
CN105885767A CN201610481675.1A CN201610481675A CN105885767A CN 105885767 A CN105885767 A CN 105885767A CN 201610481675 A CN201610481675 A CN 201610481675A CN 105885767 A CN105885767 A CN 105885767A
Authority
CN
China
Prior art keywords
component
pouring sealant
mdi
based polyurethanes
parts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201610481675.1A
Other languages
English (en)
Other versions
CN105885767B (zh
Inventor
黄金
陆南平
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.)
MIANYANG WELLS ELECTRONIC MATERIAL CO Ltd
Original Assignee
MIANYANG WELLS ELECTRONIC MATERIAL 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 MIANYANG WELLS ELECTRONIC MATERIAL CO Ltd filed Critical MIANYANG WELLS ELECTRONIC MATERIAL CO Ltd
Priority to CN201610481675.1A priority Critical patent/CN105885767B/zh
Publication of CN105885767A publication Critical patent/CN105885767A/zh
Application granted granted Critical
Publication of CN105885767B publication Critical patent/CN105885767B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
    • C09J175/04—Polyurethanes
    • C09J175/08—Polyurethanes from polyethers
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
    • C08G18/3203—Polyhydroxy compounds
    • C08G18/3206—Polyhydroxy compounds aliphatic
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/36—Hydroxylated esters of higher fatty acids
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3878—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus
    • C08G18/3882—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus having phosphorus bound to oxygen only
    • C08G18/3885—Phosphate compounds
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3878—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus
    • C08G18/3882—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus having phosphorus bound to oxygen only
    • C08G18/3887—Phosphite compounds
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3878—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus
    • C08G18/3889—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus having nitrogen in addition to phosphorus
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/4833—Polyethers containing oxyethylene units
    • C08G18/4837—Polyethers containing oxyethylene units and other oxyalkylene units
    • C08G18/4845—Polyethers containing oxyethylene units and other oxyalkylene units containing oxypropylene or higher oxyalkylene end groups
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666—Compounds of group C08G18/48 or C08G18/52
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/67—Unsaturated compounds having active hydrogen
    • C08G18/69—Polymers of conjugated dienes
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/721—Two or more polyisocyanates not provided for in one single group C08G18/73 - C08G18/80
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
    • C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
    • 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
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
    • C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
    • C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
    • C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
    • 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
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J11/00—Features of adhesives not provided for in group C09J9/00, e.g. additives
    • C09J11/02—Non-macromolecular additives
    • C09J11/04—Non-macromolecular additives inorganic
    • 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
    • C08K2201/00—Specific properties of additives
    • C08K2201/002—Physical properties
    • C08K2201/003—Additives being defined by their diameter
    • 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
    • C08K2201/00—Specific properties of additives
    • C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Inorganic Chemistry (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Sealing Material Composition (AREA)

Abstract

本发明公开了一种MDI基聚氨酯电子灌封胶及其制备方法和应用方法，该电子灌封胶由A、B两种组分组成；其中，A组分由按重量份计的50～60份的异氰酸酯、15～20份的低聚物多元醇和9～30份的反应型液体阻燃剂制成；B组分由低聚物多元醇、交联扩链剂、催化剂、填料、消泡剂和抗氧剂按一定比例制成。A、B组分按一定比例混合、固化，即制得该灌封胶。本发明通过半预聚法制备MDI基聚氨酯灌封胶，避免了NCO挥发所带来的毒性，以无卤反应型液体阻燃剂与填料协同阻燃，避免了添加型液体阻燃剂对聚氨酯灌封胶稳定性及性能的影响。所制得的聚氨酯弹性体适用于中小型电子元件的灌封。

Description

MDI基聚氨酯电子灌封胶与其制备方法和应用方法
技术领域
本发明的实施方式涉及电子器件灌封胶，属于化学领域，更具体地，本发明的实施方式涉及用于小型电子元器件封装的MDI基无卤环保聚氨酯灌封胶与其制备方法和应用方法。
背景技术
灌封胶主要有环氧灌封胶、有机硅灌封胶、聚氨酯灌封胶等。环氧灌封胶粘接性能优良、绝缘性能好，但固化后较脆、弹性差、抗冲击性能差；有机硅灌封胶绝缘性能、耐高低温抗冲击性能优异，但其耐油性及黏附力较差。聚氨酯灌封胶绝缘性能、耐水耐油性能好，同时其机械性能可调范围大、成本较低，对电器元件无腐蚀，可应用于变压器、抗流圈、转换器、电容器、电感器、变阻器、电路板、LED驱动电源等的灌封。
传统聚氨酯灌封胶的制备方法主要有一步法、预聚法和半预聚法三种。其中采用一步法制得的聚氨酯灌封胶分子结构不规整，力学性能不如预聚体法好；而采用预聚法和半预聚法制得的聚氨酯灌封胶分子链段排列比较规整，制品具有较好的力学性能，重复性也较好。
聚氨酯灌封胶应用最早的是以TDI为固化剂建立起来的聚氨酯体系，该体系多采用预聚法制备，可以保证产品具有较高的工艺性和稳定性，但由于TDI易挥发、毒性大，这就为TDI的生产、运输、应用埋下了较大的安全隐患，同时TDI体系聚氨酯灌封胶预聚体中游离NCO也会为下游行业带来环保难题。MDI体系聚氨酯灌封胶可以很大程度上规避以上难题，而以MDI代替TDI制备聚氨酯灌封胶的趋势也越来越明显。但与TDI相比，MDI的活性高、制得的预聚体粘度大，所以MDI体系聚氨酯灌封胶多以一步法制备，这就使得产品的性能及稳定性很难保证。
发明内容
为解决上述问题，同时出于聚氨酯制备工艺及环保方面的考虑，本发明提出了一种适用于小型电子元器件封装的聚氨酯灌封胶及其制备方法，尤其涉及一种MDI基无卤环保聚氨酯灌封胶及其制备方法。本发明采取的技术方案如下：
一种MDI基聚氨酯电子灌封胶，该电子灌封胶由A、B两种组分组成；其中，A组分由按重量份计的50～60份的异氰酸酯、15～20份的低聚物多元醇和9～30份的反应型液体阻燃剂制成；B组分由按重量份计的55～100份低聚物多元醇、1.0～3.5份交联扩链剂、0.01～0.1份催化剂、105～140份填料、0.5～1份消泡剂和0.5～1份抗氧剂制成。
上述MDI基聚氨酯电子灌封胶中的异氰酸酯为MDI、碳化二亚胺改性MDI、PAPI中的一种或任意几种的混合物。
上述MDI基聚氨酯电子灌封胶的A、B组分中的低聚物多元醇为羟基官能度≥2、分子量为600～5000的端羟基聚丁二烯、聚环氧丙烯多元醇、蓖麻油多元醇中的一种或任意几种的混合物。
上述MDI基聚氨酯电子灌封胶中的反应型液体阻燃剂是羟基官能度为1～2的磷酸酯类阻燃剂；填料为氧化铝、氢氧化铝或硅微粉，填料的平均粒径在1～50um的范围内。
进一步的技术方案是，上述MDI基聚氨酯电子灌封胶中的反应型液体阻燃剂为三(一缩二丙二醇)亚磷酸酯、N,N-二(2-羟基乙基)氨甲基膦酸二乙酯、N,N-二(2-羟乙基)氨甲基膦酸二甲酯、端羟基聚磷酸酯。
上述MDI基聚氨酯电子灌封胶中的交联扩链剂为丙二醇、1,4-丁二醇或三羟甲基丙烷。
上述MDI基聚氨酯电子灌封胶中的催化剂为三乙胺、三亚乙基二胺、二月桂酸二丁基锡、辛酸亚锡、异辛酸锌或异辛酸铅。
上述MDI基聚氨酯电子灌封胶中的消泡剂为改性硅氧烷、丙烯酸酯共聚物或非硅酮高分子聚合物；抗氧剂为2,6-二叔丁基-4-甲基苯酚、亚磷酸三(壬基苯酯)或酚噻嗪。
本发明还提供了上述MDI基聚氨酯电子灌封胶的制备方法，它采用半预聚法，包括以下步骤：
A组分的制备
按比例称取A组分原料，将低聚物多元醇和反应型液体阻燃剂于110～120℃下真空脱水2～3h，再降温至60～70℃，加入异氰酸酯并在30min内逐渐升温至75～85℃反应，反应过程中通氮气保护，并测试NCO％值，在NCO％值达到设定值时，停止反应即得A组分；所述设定值在10％～15％范围内；
B组分的制备
按比例称取B组分原料，将低聚物多元醇、交联扩链剂、填料加入反应釜中并于110～120℃下真空搅拌2h，再降温至50～80℃，加入消泡剂、催化剂和抗氧剂，搅拌均匀即得B组分。
上述MDI基聚氨酯电子灌封胶的应用方法是：所述A组分和B组分按照质量比20～25:100混合后搅拌、脱泡，浇注于经干燥处理过的电子器件中，再于25℃固化7天或者于60℃固化24h，即完成电子器件的灌封。
与现有技术相比，本发明的有益效果之一是：本发明通过半预聚法制备MDI基聚氨酯灌封胶，既避免了TDI基聚氨酯灌封胶预聚体中游离NCO挥发所带来的毒性，又改善了MDI基聚氨酯灌封胶的制备工艺；同时该体系以无卤反应型液体阻燃剂与填料协同阻燃，由于阻燃剂分子结合到聚氨酯分子结构中，耐迁移、具有低成雾性及持久的阻燃性能，规避了阻燃剂对灌封胶稳定性及性能的影响。该体系所用原材料安全无毒、成本低廉，配方设计科学合理，操作简单易行。所制得的聚氨酯弹性体适用于中小型电子元件的灌封，且其固化速度可调，可室温或加温固化，储存稳定，具有良好的附着力、耐水性、阻燃性、导热性及电气性能。
具体实施方式
为了使本发明的目的、技术方案及优点更加清楚明白，以下结合实施例，对本发明进行进一步详细说明。应当理解，此处所描述的具体实施例仅仅用以解释本发明，并不用于限定本发明。
实施例1
(1)A组分的制备：将20kg聚丙二醇(MN＝2000)、30kg端羟基聚磷酸酯(羟值为170mgKOH/g)加入到反应器中并于110℃下真空脱水3h，再降温至65℃，加入20kg4,4-二苯基甲烷二异氰酸酯、30kg多亚甲基多苯基多异氰酸酯，并在30min内逐渐升温至80℃反应，反应过程中通氮气保护，并测试NCO％值，在NCO％值达到11％时停止反应，即制得A组分。
(2)B组分的制备：将75kg聚丙二醇(MN＝3000)、22kg蓖麻油(羟值为170mgKOH/g)、3kg1,4-丁二醇、119kg氧化铝加入反应釜中并于115℃下真空搅拌2h，再降温至75℃，加入0.5kg消泡剂、0.01kg催化剂、0.5kg抗氧剂搅拌均匀即制得B组分。
(3)将A、B组分按重量比为20：100的比例称量、搅拌、脱泡后，浇筑于经干燥处理过的电子器件中，再于25℃固化7天。
实施例2
(1)A组分的制备：将20kg聚丙二醇(MN＝2000)、9kg三(一缩二丙二醇)亚磷酸酯(羟值为395mgKOH/g)加入到反应器中并于115℃下真空脱水2h，再降温至70℃，加入50kg液化4,4-二苯基甲烷二异氰酸酯，并在在30min内逐渐升温至85℃反应，反应过程中通氮气保护，并测试NCO％值，在NCO％值达到15％时停止反应，即制得A组分。
(2)B组分的制备：将72kg聚丙二醇(MN＝2000)、17kg蓖麻油(羟值为170mgKOH/g)、1kg丙二醇、50kg氧化铝、59kg氢氧化铝加入反应釜中并于120℃下真空搅拌2h，再降温至80℃，加入0.5kg消泡剂、0.01kg催化剂、0.5kg抗氧剂搅拌均匀即制得B组分。
(3)将A、B组分按重量比为20：100的比例称量、搅拌、脱泡后，浇筑于经干燥处理过的电子器件中，再于60℃固化24h。
实施例3
(1)A组分的制备：将15g聚丙二醇(MN＝2000)、12.5gN,N-二(2-羟乙基)氨甲基膦酸二乙酯(羟值为450mgKOH/g)加入到反应器中并于120℃下真空脱水2h，再降温至60℃，加入35g4,4-二苯基甲烷二异氰酸酯、15g多亚甲基多苯基多异氰酸酯并在30min内逐渐升温至75℃反应，反应过程中通氮气保护，并测试NCO％值，在NCO％值达到15％时停止反应，即制得A组分。
(2)B组分的制备：将39kg端羟基聚丁二烯(羟值为60mgKOH/g)、29kg蓖麻油(羟值为170mgKOH/g)、2kg1,4-丁二醇和129kg氢氧化铝加入反应釜中并于110℃下真空搅拌2h，再降温至60℃，加入0.5kg消泡剂、0.01kg催化剂、0.5kg抗氧剂搅拌均匀即制得B组分。
(3)将A、B组分按重量比为25：100的比例称量、搅拌、脱泡后，浇筑于经干燥处理过的电子器件中，再于25℃固化7天或于60℃固化24h。
实施例4
(1)A组分的制备：将15g聚丙二醇(MN＝2000)、10.5gN,N-二(2-羟乙基)氨甲基膦酸二甲酯(羟值为480mgKOH/g)加入到反应器中并于120℃下真空脱水2h，再降温至65℃，加入40g4,4-二苯基甲烷二异氰酸酯、10g多亚甲基多苯基多异氰酸酯并在30min内逐渐升温至75℃反应，反应过程中通氮气保护，并测试NCO％值，在NCO％值达到14％时停止反应，即制得A组分。
(2)B组分的制备：将17.2kg端羟基聚丁二烯(羟值为60mgKOH/g)、39.7kg聚丙二醇(MN＝2000)、3.1kg三羟甲基丙烷和139kg硅微粉加入反应釜中并于110℃下真空搅拌2h，再降温至50℃，加入0.5kg消泡剂、0.01kg催化剂、0.5kg抗氧剂搅拌均匀即制得B组分。
(3)将A、B组分按重量比为20：100的比例称量、搅拌、脱泡后，浇筑于经干燥处理过的电子器件中，再于25℃固化7天或于60℃固化24h。
上述实施例1～4所得产品的性能如表1所示。
表1各实施例性能对比
从上表可以看出，实施例1～4所制得的聚氨酯弹性体都具有较高的力学性能和导热性能，同时由于本发明无外加增塑剂和非反应型液体阻燃剂，这就使得该发明制备的聚氨酯灌封胶具有较高的阻燃性能和电性能。
尽管这里参照本发明的解释性实施例对本发明进行了描述，但是，应该理解，本领域技术人员可以设计出很多其他的修改和实施方式，这些修改和实施方式将落在本申请公开的原则范围和精神之内。更具体地说，在本申请公开的范围内，可以对主题组合布局的组成部件和/或布局进行多种变型和改进。除了对组成部件和/或布局进行的变型和改进外，对于本领域技术人员来说，其他的用途也将是明显的。

Claims (10)

1.一种MDI基聚氨酯电子灌封胶，其特征在于该电子灌封胶由A、B两种组分组成；其中，A组分由按重量份计的50～60份的异氰酸酯、15～20份的低聚物多元醇和9～30份的反应型液体阻燃剂制成；B组分由按重量份计的55～100份低聚物多元醇、1.0～3.5份交联扩链剂、0.01～0.1份催化剂、105～140份填料、0.5～1份消泡剂和0.5～1份抗氧剂制成。
2.根据权利要求1所述的MDI基聚氨酯电子灌封胶，其特征在于所述异氰酸酯为MDI、碳化二亚胺改性MDI、PAPI中的一种或任意几种的混合物。
3.根据权利要求1所述的MDI基聚氨酯电子灌封胶，其特征在于A、B组分中所述低聚物多元醇为羟基官能度≥2、分子量为600～5000的端羟基聚丁二烯、聚环氧丙烯多元醇、蓖麻油多元醇中的一种或任意几种的混合物。
4.根据权利要求1所述的MDI基聚氨酯电子灌封胶，其特征在于所述反应型液体阻燃剂是羟基官能度为1～2的磷酸酯类阻燃剂；所述填料为氧化铝、氢氧化铝或硅微粉，填料的平均粒径在1～50um的范围内。
5.根据权利要求4所述的MDI基聚氨酯电子灌封胶，其特征在于所述反应型液体阻燃剂为三(一缩二丙二醇)亚磷酸酯、N,N-二(2-羟基乙基)氨甲基膦酸二乙酯、N,N-二(2-羟乙基)氨甲基膦酸二甲酯、端羟基聚磷酸酯。
6.根据权利要求1所述的MDI基聚氨酯电子灌封胶，其特征在于所述交联扩链剂为丙二醇、1,4-丁二醇或三羟甲基丙烷。
7.根据权利要求1所述的MDI基聚氨酯电子灌封胶，其特征在于所述催化剂为三乙胺、三亚乙基二胺、二月桂酸二丁基锡、辛酸亚锡、异辛酸锌或异辛酸铅。
8.根据权利要求1所述的MDI基聚氨酯电子灌封胶，其特征在于所述消泡剂为改性硅氧烷、丙烯酸酯共聚物或非硅酮高分子聚合物；所述抗氧剂为2,6-二叔丁基-4-甲基苯酚、亚磷酸三(壬基苯酯)或酚噻嗪。
9.如权利要求1～8任意一项所述的MDI基聚氨酯电子灌封胶的制备方法，其特征在于它采用半预聚法，包括以下步骤：
A组分的制备
按比例称取A组分原料，将低聚物多元醇和反应型液体阻燃剂于110～120℃下真空脱水2～3h，再降温至60～70℃，加入异氰酸酯并在30min内逐渐升温至75～85℃反应，反应过程中通氮气保护，并测试NCO％值，在NCO％值达到设定值时，停止反应即得A组分；所述设定值在10％～15％范围内；
B组分的制备
按比例称取B组分原料，将低聚物多元醇、交联扩链剂、填料加入反应釜中并于110～120℃下真空搅拌2h，再降温至50～80℃，加入消泡剂、催化剂和抗氧剂，搅拌均匀即得B组分。
10.如权利要求1～8任意一项所述的MDI基聚氨酯电子灌封胶的应用方法，其特征在于所述A组分和B组分按照质量比20～25:100混合后搅拌、脱泡，浇注于经干燥处理过的电子器件中，再于25℃固化7天或者于60℃固化24h，即完成电子器件的灌封。
CN201610481675.1A 2016-06-24 2016-06-24 Mdi基聚氨酯电子灌封胶与其制备方法和应用方法 Active CN105885767B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610481675.1A CN105885767B (zh) 2016-06-24 2016-06-24 Mdi基聚氨酯电子灌封胶与其制备方法和应用方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610481675.1A CN105885767B (zh) 2016-06-24 2016-06-24 Mdi基聚氨酯电子灌封胶与其制备方法和应用方法

Publications (2)

Publication Number Publication Date
CN105885767A true CN105885767A (zh) 2016-08-24
CN105885767B CN105885767B (zh) 2019-02-19

Family

ID=56718420

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610481675.1A Active CN105885767B (zh) 2016-06-24 2016-06-24 Mdi基聚氨酯电子灌封胶与其制备方法和应用方法

Country Status (1)

Country Link
CN (1) CN105885767B (zh)

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108084944A (zh) * 2016-11-21 2018-05-29 日胜化工股份有限公司 基材适应性广的双涂布快速固化无溶剂聚氨酯接着剂、复合膜材及其制备方法
CN108659772A (zh) * 2017-03-29 2018-10-16 孚能科技（赣州）有限公司 灌封胶和电池组
CN108666464A (zh) * 2017-03-29 2018-10-16 孚能科技（赣州）有限公司 灌封胶和电池组
CN109593507A (zh) * 2018-12-17 2019-04-09 烟台德邦科技有限公司 一种用于软包电池电芯粘接的聚氨酯胶黏剂
CN109679319A (zh) * 2018-11-12 2019-04-26 许文强 一种高导热低热膨胀的电子封装材料的制备方法
CN109679566A (zh) * 2018-12-17 2019-04-26 株洲时代新材料科技股份有限公司 一种高性能聚氨酯灌封胶及其制备方法与使用方法
CN109777339A (zh) * 2019-01-23 2019-05-21 创达惠利新材料(成都)有限公司 用于高湿热环境的阻燃型聚氨酯灌封胶、制备及使用方法
CN110964311A (zh) * 2018-09-30 2020-04-07 天津市橡胶工业研究所有限公司 低密度聚氨酯灌封材料及制备方法
CN111808570A (zh) * 2020-08-27 2020-10-23 格丽泰新材料科技（苏州）有限公司 一种双组份聚氨酯粘合剂及其应用
CN112029393A (zh) * 2020-07-27 2020-12-04 湖北南北车新材料有限公司 一种双组份聚氨酯涂层及制备方法
CN112608707A (zh) * 2020-12-15 2021-04-06 广东普赛达密封粘胶有限公司 一种双组分聚氨酯结构胶及其制备方法
CN113088237A (zh) * 2021-05-25 2021-07-09 长兴圣凯利新材料有限公司 一种环保型高性能聚氨酯灌封胶及其制备方法
WO2021243817A1 (zh) * 2020-06-03 2021-12-09 山东一诺威聚氨酯股份有限公司 导热无卤阻燃聚氨酯弹性体及其制备方法
CN114316878A (zh) * 2021-12-07 2022-04-12 黎明化工研究设计院有限责任公司 一种聚氨酯灌封胶及其制备方法和用途
CN114686154A (zh) * 2022-03-01 2022-07-01 深圳镝普材料科技有限公司 一种热至相变阻尼灌封胶粘剂及其制备方法
CN115521752A (zh) * 2022-11-09 2022-12-27 江苏博韵低维材料科技有限公司 一种高导热灌封胶及其制备方法
WO2023109163A1 (zh) * 2021-12-14 2023-06-22 道生天合材料科技(上海)股份有限公司 聚氨酯凝胶及其制备方法
CN116554825A (zh) * 2023-07-12 2023-08-08 山东理工大学 耐候丙烯酸酯聚氨酯灌封胶及其制备方法
WO2023178660A1 (en) * 2022-03-25 2023-09-28 Rohm and Haas Electronic Materials (Shanghai) Ltd. Two-component polyurethane adhesive

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102643623A (zh) * 2012-04-05 2012-08-22 艾伦塔斯电气绝缘材料(珠海)有限公司 一种高粘结强度聚氨酯树脂灌封胶及其制备方法

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102643623A (zh) * 2012-04-05 2012-08-22 艾伦塔斯电气绝缘材料(珠海)有限公司 一种高粘结强度聚氨酯树脂灌封胶及其制备方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
刘益军: "《聚氨酯原料及助剂手册》", 30 April 2005 *

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108084944A (zh) * 2016-11-21 2018-05-29 日胜化工股份有限公司 基材适应性广的双涂布快速固化无溶剂聚氨酯接着剂、复合膜材及其制备方法
CN108659772A (zh) * 2017-03-29 2018-10-16 孚能科技（赣州）有限公司 灌封胶和电池组
CN108666464A (zh) * 2017-03-29 2018-10-16 孚能科技（赣州）有限公司 灌封胶和电池组
CN110964311A (zh) * 2018-09-30 2020-04-07 天津市橡胶工业研究所有限公司 低密度聚氨酯灌封材料及制备方法
CN109679319A (zh) * 2018-11-12 2019-04-26 许文强 一种高导热低热膨胀的电子封装材料的制备方法
CN109593507A (zh) * 2018-12-17 2019-04-09 烟台德邦科技有限公司 一种用于软包电池电芯粘接的聚氨酯胶黏剂
CN109679566A (zh) * 2018-12-17 2019-04-26 株洲时代新材料科技股份有限公司 一种高性能聚氨酯灌封胶及其制备方法与使用方法
CN109777339A (zh) * 2019-01-23 2019-05-21 创达惠利新材料(成都)有限公司 用于高湿热环境的阻燃型聚氨酯灌封胶、制备及使用方法
WO2021243817A1 (zh) * 2020-06-03 2021-12-09 山东一诺威聚氨酯股份有限公司 导热无卤阻燃聚氨酯弹性体及其制备方法
CN112029393B (zh) * 2020-07-27 2022-06-07 湖北南北车新材料有限公司 一种双组份聚氨酯涂层及制备方法
CN112029393A (zh) * 2020-07-27 2020-12-04 湖北南北车新材料有限公司 一种双组份聚氨酯涂层及制备方法
CN111808570A (zh) * 2020-08-27 2020-10-23 格丽泰新材料科技（苏州）有限公司 一种双组份聚氨酯粘合剂及其应用
CN112608707A (zh) * 2020-12-15 2021-04-06 广东普赛达密封粘胶有限公司 一种双组分聚氨酯结构胶及其制备方法
CN112608707B (zh) * 2020-12-15 2022-12-13 广东普赛达密封粘胶有限公司 一种双组分聚氨酯结构胶及其制备方法
CN113088237A (zh) * 2021-05-25 2021-07-09 长兴圣凯利新材料有限公司 一种环保型高性能聚氨酯灌封胶及其制备方法
CN113088237B (zh) * 2021-05-25 2022-12-02 长兴圣凯利新材料有限公司 一种环保型高性能聚氨酯灌封胶及其制备方法
CN114316878A (zh) * 2021-12-07 2022-04-12 黎明化工研究设计院有限责任公司 一种聚氨酯灌封胶及其制备方法和用途
WO2023109163A1 (zh) * 2021-12-14 2023-06-22 道生天合材料科技(上海)股份有限公司 聚氨酯凝胶及其制备方法
CN114686154A (zh) * 2022-03-01 2022-07-01 深圳镝普材料科技有限公司 一种热至相变阻尼灌封胶粘剂及其制备方法
CN114686154B (zh) * 2022-03-01 2023-09-26 深圳镝普材料科技有限公司 一种热至相变阻尼灌封胶粘剂及其制备方法
WO2023178660A1 (en) * 2022-03-25 2023-09-28 Rohm and Haas Electronic Materials (Shanghai) Ltd. Two-component polyurethane adhesive
CN115521752A (zh) * 2022-11-09 2022-12-27 江苏博韵低维材料科技有限公司 一种高导热灌封胶及其制备方法
CN116554825A (zh) * 2023-07-12 2023-08-08 山东理工大学 耐候丙烯酸酯聚氨酯灌封胶及其制备方法
CN116554825B (zh) * 2023-07-12 2023-10-20 山东理工大学 耐候丙烯酸酯聚氨酯灌封胶及其制备方法

Also Published As

Publication number Publication date
CN105885767B (zh) 2019-02-19

Similar Documents

Publication Publication Date Title
CN105885767A (zh) Mdi基聚氨酯电子灌封胶与其制备方法和应用方法
CN112608707B (zh) 一种双组分聚氨酯结构胶及其制备方法
CN102102006B (zh) 一种双组分聚氨酯灌封胶的制备方法及其制品
CN112322028B (zh) 一种聚氨酯低密度导热凝胶及其制备方法
KR102355209B1 (ko) 전자 회로 조립체를 플러드 코팅하기 위한 배합 폴리우레탄 수지 조성물
US9376564B2 (en) Polyurethane casting resins and potting compounds produced therefrom
CN111849410A (zh) 无卤阻燃导热聚氨酯灌封胶及其制备方法
JP2003504422A (ja) 使用温度が高いポリウレタンエラストマー
CN106047268A (zh) 电子灌封用双组份聚氨酯胶粘剂及其制备方法
CN109762502A (zh) 一种无卤环保阻燃型聚氨酯密封胶及其制备方法
CN109880578A (zh) 一种双组份低硬度耐热聚氨酯灌封胶及其制备方法
JP7396193B2 (ja) ウレタン樹脂組成物及びその硬化物
KR102091129B1 (ko) 알로파네이트 및 소수성 수지의 조성물
US6225377B1 (en) Blending epoxy resin-polyisocyanate-filler mixture and phenolic resin-filler mixture for molding
CN101847506A (zh) 一种大功率电抗器的封装方法
KR20160097829A (ko) 폴리티올 경화제를 포함하는 에폭시 접착제 조성물 및 이의 제조방법
JP2010150472A (ja) ポリウレタン樹脂組成物及びポリウレタン樹脂
CN111892901A (zh) 一种中空玻璃用快固化双组份聚氨酯密封胶及其制备方法
CN110669466A (zh) 无卤阻燃耐水解聚氨酯灌封胶及其制备方法
CN114634788B (zh) 聚氨酯胶黏剂及其制备方法
CN116376502B (zh) 有机硅树脂改性聚氨酯灌封胶及其制备方法
JP2018021141A (ja) ポリウレタン樹脂組成物
CN111592852A (zh) 低粘度高力学性能的聚氨酯灌封胶及其制备方法和应用
JPH02202908A (ja) ウレタン組成物
KR101899407B1 (ko) 블록화된 반응형 계면활성제를 이용한 수분산 이소시아네이트의 제조방법 및 이에 의해 제조되는 수분산 이소시아네이트

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant