CN103183962A - 具有改善的导热性和表观的聚苯硫醚树脂组合物和其制品 - Google Patents
具有改善的导热性和表观的聚苯硫醚树脂组合物和其制品 Download PDFInfo
- Publication number
- CN103183962A CN103183962A CN2012105749099A CN201210574909A CN103183962A CN 103183962 A CN103183962 A CN 103183962A CN 2012105749099 A CN2012105749099 A CN 2012105749099A CN 201210574909 A CN201210574909 A CN 201210574909A CN 103183962 A CN103183962 A CN 103183962A
- Authority
- CN
- China
- Prior art keywords
- resin composition
- polyphenyl thioether
- combination
- heat conductive
- conductive insulating
- 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
Links
- 239000011342 resin composition Substances 0.000 title claims abstract description 47
- 239000004734 Polyphenylene sulfide Substances 0.000 title claims abstract description 32
- 229920000069 polyphenylene sulfide Polymers 0.000 title claims abstract description 32
- 229920005989 resin Polymers 0.000 claims abstract description 65
- 239000011347 resin Substances 0.000 claims abstract description 65
- 239000000945 filler Substances 0.000 claims abstract description 56
- 229920006020 amorphous polyamide Polymers 0.000 claims abstract description 28
- 229920006389 polyphenyl polymer Polymers 0.000 claims description 35
- 150000003568 thioethers Chemical class 0.000 claims description 35
- 238000002360 preparation method Methods 0.000 claims description 24
- 239000000126 substance Substances 0.000 claims description 22
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 18
- 239000000395 magnesium oxide Substances 0.000 claims description 16
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 16
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 14
- 239000000654 additive Substances 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 10
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 9
- 230000000996 additive effect Effects 0.000 claims description 7
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 claims description 7
- SYECJBOWSGTPLU-UHFFFAOYSA-N hexane-1,1-diamine Chemical compound CCCCCC(N)N SYECJBOWSGTPLU-UHFFFAOYSA-N 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
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 claims description 5
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 claims description 5
- 239000003063 flame retardant Substances 0.000 claims description 5
- DLYLVPHSKJVGLG-UHFFFAOYSA-N 4-(cyclohexylmethyl)cyclohexane-1,1-diamine Chemical compound C1CC(N)(N)CCC1CC1CCCCC1 DLYLVPHSKJVGLG-UHFFFAOYSA-N 0.000 claims description 4
- 150000001408 amides Chemical class 0.000 claims description 4
- 230000005855 radiation Effects 0.000 claims description 4
- PIGFYZPCRLYGLF-UHFFFAOYSA-N Aluminum nitride Chemical compound [Al]#N PIGFYZPCRLYGLF-UHFFFAOYSA-N 0.000 claims description 3
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 230000007704 transition Effects 0.000 claims description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 2
- 230000003078 antioxidant effect Effects 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 239000003381 stabilizer Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 10
- 229910052751 metal Inorganic materials 0.000 description 10
- 239000002184 metal Substances 0.000 description 10
- -1 nitro, phenyl Chemical group 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 230000000704 physical effect Effects 0.000 description 9
- 238000012856 packing Methods 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 6
- 239000013078 crystal Substances 0.000 description 6
- 239000002932 luster Substances 0.000 description 6
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 239000004519 grease Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920006122 polyamide resin Polymers 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000000919 ceramic Substances 0.000 description 4
- 230000006872 improvement Effects 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- WTKWFNIIIXNTDO-UHFFFAOYSA-N 3-isocyanato-5-methyl-2-(trifluoromethyl)furan Chemical compound CC1=CC(N=C=O)=C(C(F)(F)F)O1 WTKWFNIIIXNTDO-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 208000034189 Sclerosis Diseases 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- GWZCCUDJHOGOSO-UHFFFAOYSA-N diphenic acid Chemical compound OC(=O)C1=CC=CC=C1C1=CC=CC=C1C(O)=O GWZCCUDJHOGOSO-UHFFFAOYSA-N 0.000 description 2
- 229920002313 fluoropolymer Polymers 0.000 description 2
- 239000004811 fluoropolymer Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 230000017525 heat dissipation Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- TVIDDXQYHWJXFK-UHFFFAOYSA-N n-Dodecanedioic acid Natural products OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 description 2
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Natural products OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 description 2
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- DWFUTNJGNBYHNN-UHFFFAOYSA-N 2,2,4-trimethylhexanedioic acid Chemical compound OC(=O)CC(C)CC(C)(C)C(O)=O DWFUTNJGNBYHNN-UHFFFAOYSA-N 0.000 description 1
- RLEQVGMLDNITBW-UHFFFAOYSA-N 2,4,4-trimethylhexanedioic acid Chemical compound OC(=O)C(C)CC(C)(C)CC(O)=O RLEQVGMLDNITBW-UHFFFAOYSA-N 0.000 description 1
- AIDLAEPHWROGFI-UHFFFAOYSA-N 2-methylbenzene-1,3-dicarboxylic acid Chemical compound CC1=C(C(O)=O)C=CC=C1C(O)=O AIDLAEPHWROGFI-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- IGSBHTZEJMPDSZ-UHFFFAOYSA-N 4-[(4-amino-3-methylcyclohexyl)methyl]-2-methylcyclohexan-1-amine Chemical compound C1CC(N)C(C)CC1CC1CC(C)C(N)CC1 IGSBHTZEJMPDSZ-UHFFFAOYSA-N 0.000 description 1
- DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 description 1
- OAPDPORYXWQVJE-UHFFFAOYSA-N 4-propylaniline Chemical compound CCCC1=CC=C(N)C=C1 OAPDPORYXWQVJE-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- 229910052582 BN Inorganic materials 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000002134 carbon nanofiber Substances 0.000 description 1
- 229910021393 carbon nanotube Inorganic materials 0.000 description 1
- 239000002041 carbon nanotube Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000011231 conductive filler Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- 238000010292 electrical insulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229940033355 lauric acid Drugs 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- ABMFBCRYHDZLRD-UHFFFAOYSA-N naphthalene-1,4-dicarboxylic acid Chemical group C1=CC=C2C(C(=O)O)=CC=C(C(O)=O)C2=C1 ABMFBCRYHDZLRD-UHFFFAOYSA-N 0.000 description 1
- DFFZOPXDTCDZDP-UHFFFAOYSA-N naphthalene-1,5-dicarboxylic acid Chemical group C1=CC=C2C(C(=O)O)=CC=CC2=C1C(O)=O DFFZOPXDTCDZDP-UHFFFAOYSA-N 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical group C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- WPUMVKJOWWJPRK-UHFFFAOYSA-N naphthalene-2,7-dicarboxylic acid Chemical group C1=CC(C(O)=O)=CC2=CC(C(=O)O)=CC=C21 WPUMVKJOWWJPRK-UHFFFAOYSA-N 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- UMRZSTCPUPJPOJ-KNVOCYPGSA-N norbornane Chemical compound C1C[C@H]2CC[C@@H]1C2 UMRZSTCPUPJPOJ-KNVOCYPGSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- DEDZSLCZHWTGOR-UHFFFAOYSA-N propylcyclohexane Chemical compound CCCC1CCCCC1 DEDZSLCZHWTGOR-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 230000035924 thermogenesis Effects 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/04—Polysulfides
-
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/38—Boron-containing compounds
-
- 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
- C08K7/00—Use of ingredients characterised by shape
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/02—Polythioethers; Polythioether-ethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/48—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor body packages
- H01L33/64—Heat extraction or cooling elements
- H01L33/641—Heat extraction or cooling elements characterized by the materials
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
Claims (12)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020110146941A KR101437880B1 (ko) | 2011-12-30 | 2011-12-30 | 표면 광택이 우수한 폴리페닐렌설파이드계 열전도성 수지 조성물 및 이를 이용한 성형품 |
KR10-2011-0146941 | 2011-12-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN103183962A true CN103183962A (zh) | 2013-07-03 |
CN103183962B CN103183962B (zh) | 2016-01-06 |
Family
ID=48675418
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201210574909.9A Active CN103183962B (zh) | 2011-12-30 | 2012-12-26 | 具有改善的导热性和表观的聚苯硫醚树脂组合物和其制品 |
Country Status (4)
Country | Link |
---|---|
US (1) | US8765858B2 (zh) |
KR (1) | KR101437880B1 (zh) |
CN (1) | CN103183962B (zh) |
TW (1) | TWI540180B (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103665868A (zh) * | 2013-12-07 | 2014-03-26 | 天津市华鑫达投资有限公司 | 一种无卤阻燃导热绝缘树脂组合物及其制备方法 |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101457016B1 (ko) * | 2011-12-30 | 2014-11-03 | 제일모직주식회사 | 내습성 및 열전도성이 우수한 열가소성 수지 조성물 및 성형품 |
KR101668432B1 (ko) * | 2014-09-30 | 2016-10-21 | 자동차부품연구원 | 발열 특성 제어를 위한 방열복합소재 |
WO2016057418A1 (en) * | 2014-10-07 | 2016-04-14 | Polyone Corporation | Thermally conductive polymer articles for electronic circuitry |
CN106633881A (zh) * | 2016-12-14 | 2017-05-10 | 深圳市鼎盛新材料有限公司 | 一种pps导热绝缘塑料的制备方法 |
CN115135484A (zh) * | 2019-12-17 | 2022-09-30 | 提克纳有限责任公司 | 使用聚芳硫醚粉末的粉末床熔合打印系统 |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1775860A (zh) * | 2005-11-25 | 2006-05-24 | 华南理工大学 | 注射成型的导热绝缘塑料 |
JP2006342192A (ja) * | 2005-06-07 | 2006-12-21 | Daisee Kogyo Kk | 電気絶縁性でかつ熱伝導性に優れた成形用樹脂 |
CN101717579A (zh) * | 2009-10-30 | 2010-06-02 | 华南理工大学 | 填充型导热绝缘聚苯硫醚与聚酰胺共混合金及其制备方法 |
CN101899209A (zh) * | 2010-03-30 | 2010-12-01 | 金发科技股份有限公司 | 一种导热绝缘材料及其制备方法 |
CN102070899A (zh) * | 2010-12-30 | 2011-05-25 | 广东银禧科技股份有限公司 | 一种绝缘导热聚酰胺复合材料及制备方法 |
CN102079864A (zh) * | 2009-11-30 | 2011-06-01 | 比亚迪股份有限公司 | 一种绝缘导热树脂组合物及其塑胶制品 |
CN102174254A (zh) * | 2010-12-27 | 2011-09-07 | 东莞劲胜精密组件股份有限公司 | 一种高导热绝缘工程塑料及其制备方法 |
CN102250481A (zh) * | 2011-05-25 | 2011-11-23 | 上海树普新材料科技有限公司 | 高导热塑料及其制备方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5212240A (en) | 1975-07-18 | 1977-01-29 | Matsushita Electric Ind Co Ltd | Process for preparing transparent coating compounds |
US4528335A (en) | 1984-05-18 | 1985-07-09 | Phillips Petroleum Company | Polymer blends |
EP0450753A3 (en) * | 1990-04-04 | 1992-03-25 | Tonen Chemical Corporation | Poly (arylene sulfide) resin composition |
KR101028652B1 (ko) | 2003-06-05 | 2011-04-11 | 도레이 카부시키가이샤 | 폴리페닐렌 술피드 수지 조성물 |
JP2009202567A (ja) * | 2008-02-01 | 2009-09-10 | Techno Polymer Co Ltd | 樹脂製部材及び金属製部材からなる複合体の製造方法並びにled実装用基板及びled用リフレクター |
-
2011
- 2011-12-30 KR KR1020110146941A patent/KR101437880B1/ko active IP Right Grant
-
2012
- 2012-12-21 US US13/723,363 patent/US8765858B2/en active Active
- 2012-12-26 CN CN201210574909.9A patent/CN103183962B/zh active Active
- 2012-12-27 TW TW101150360A patent/TWI540180B/zh not_active IP Right Cessation
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006342192A (ja) * | 2005-06-07 | 2006-12-21 | Daisee Kogyo Kk | 電気絶縁性でかつ熱伝導性に優れた成形用樹脂 |
CN1775860A (zh) * | 2005-11-25 | 2006-05-24 | 华南理工大学 | 注射成型的导热绝缘塑料 |
CN101717579A (zh) * | 2009-10-30 | 2010-06-02 | 华南理工大学 | 填充型导热绝缘聚苯硫醚与聚酰胺共混合金及其制备方法 |
CN102079864A (zh) * | 2009-11-30 | 2011-06-01 | 比亚迪股份有限公司 | 一种绝缘导热树脂组合物及其塑胶制品 |
CN101899209A (zh) * | 2010-03-30 | 2010-12-01 | 金发科技股份有限公司 | 一种导热绝缘材料及其制备方法 |
CN102174254A (zh) * | 2010-12-27 | 2011-09-07 | 东莞劲胜精密组件股份有限公司 | 一种高导热绝缘工程塑料及其制备方法 |
CN102070899A (zh) * | 2010-12-30 | 2011-05-25 | 广东银禧科技股份有限公司 | 一种绝缘导热聚酰胺复合材料及制备方法 |
CN102250481A (zh) * | 2011-05-25 | 2011-11-23 | 上海树普新材料科技有限公司 | 高导热塑料及其制备方法 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103665868A (zh) * | 2013-12-07 | 2014-03-26 | 天津市华鑫达投资有限公司 | 一种无卤阻燃导热绝缘树脂组合物及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
TWI540180B (zh) | 2016-07-01 |
TW201333115A (zh) | 2013-08-16 |
CN103183962B (zh) | 2016-01-06 |
KR101437880B1 (ko) | 2014-09-12 |
US8765858B2 (en) | 2014-07-01 |
US20130172466A1 (en) | 2013-07-04 |
KR20130078154A (ko) | 2013-07-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103183962B (zh) | 具有改善的导热性和表观的聚苯硫醚树脂组合物和其制品 | |
JP6671869B2 (ja) | 液晶ポリエステル樹脂組成物、コネクターおよび液晶ポリエステル樹脂組成物の製造方法 | |
CN103183956B (zh) | 具有改进的导热性的热塑性树脂组合物及其制品 | |
EP2195374B1 (en) | Heat-processable thermally conductive polymer composition | |
JP5633338B2 (ja) | 液晶ポリエステル組成物 | |
CN108602966A (zh) | 成形品及其制造方法 | |
TW200911923A (en) | Polyarylene sulfide resin composition and molded product comprising the same | |
JP2015168783A (ja) | 高熱伝導性樹脂組成物 | |
CN102702700B (zh) | 高流动低翘曲液晶聚合物组合物及其制备方法和应用 | |
JP2006328352A (ja) | 絶縁性熱伝導性樹脂組成物及び成形品並びにその製造方法 | |
TW200812834A (en) | Lamp sockets | |
JP2013028661A (ja) | 樹脂組成物およびそれからなる成形体 | |
JP5966931B2 (ja) | 難燃性ポリアミド樹脂組成物およびそれからなる成形品 | |
WO2008063709A2 (en) | Thermally conductive polymer compounds containing zinc sulfide | |
JP5618039B2 (ja) | 熱伝導性樹脂組成物およびそれからなる成形体 | |
JP2013001802A (ja) | 熱伝導性樹脂組成物およびそれからなる成形体 | |
CN101490472B (zh) | 灯座 | |
KR101446707B1 (ko) | 분산특성이 우수한 필러를 포함하는 전기절연성 및 열전도성 고분자 조성물, 이의 제조방법 및 이를 포함하는 성형품 | |
JP2010043229A (ja) | 伝熱性樹脂組成物およびその樹脂成形体 | |
KR101380841B1 (ko) | 열전도성 및 내열성을 갖는 고분자 조성물의 성형품 제조방법 및 이에 의해 제조되는 열전도성 및 내열성을 갖는 고분자 조성물의 성형품 | |
KR20140121161A (ko) | 전기절연성 및 열전도성 고분자 조성물, 이의 제조방법 및 이를 포함하는 성형품 | |
WO2021235277A1 (ja) | 熱伝導性樹脂組成物およびそれからなる成形体 | |
JP2017190407A (ja) | ポリアミド樹脂組成物およびそれからなる成形体 | |
JP2021113308A (ja) | 熱伝導性樹脂組成物およびそれからなる成形体 | |
JP6371159B2 (ja) | 熱伝導性樹脂組成物およびそれからなる成形体 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20170307 Address after: Jeonnam, South Korea Patentee after: LOTTE ADVANCED MATERIALS Co.,Ltd. Address before: Gyeonggi Do, South Korea Patentee before: Samsung SDI Co.,Ltd. Effective date of registration: 20170307 Address after: Gyeonggi Do, South Korea Patentee after: Samsung SDI Co.,Ltd. Address before: Gyeongbuk, South Korea Patentee before: Cheil Industries Inc. |