JPH0210183B2 - - Google Patents
Info
- Publication number
- JPH0210183B2 JPH0210183B2 JP7767882A JP7767882A JPH0210183B2 JP H0210183 B2 JPH0210183 B2 JP H0210183B2 JP 7767882 A JP7767882 A JP 7767882A JP 7767882 A JP7767882 A JP 7767882A JP H0210183 B2 JPH0210183 B2 JP H0210183B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- polyamide resin
- parts
- tetramethylpiperidine
- substituted
- 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.)
- Expired
Links
- 229920006122 polyamide resin Polymers 0.000 claims description 22
- -1 carbamoyloxy group Chemical group 0.000 claims description 14
- 239000011342 resin composition Substances 0.000 claims description 14
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 claims description 11
- 150000003053 piperidines Chemical class 0.000 claims description 10
- 238000000465 moulding Methods 0.000 claims description 9
- 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 claims description 6
- 239000003063 flame retardant Substances 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 125000004423 acyloxy group Chemical group 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000005530 alkylenedioxy group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- AYOCQODSVOEOHO-UHFFFAOYSA-N carbamoyl carbamate Chemical group NC(=O)OC(N)=O AYOCQODSVOEOHO-UHFFFAOYSA-N 0.000 claims description 2
- 125000005587 carbonate group Chemical group 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 239000000047 product Substances 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000008188 pellet Substances 0.000 description 5
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 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
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- SQRYDOGPOHDUKZ-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) 2-methylbenzoate Chemical compound CC1=CC=CC=C1C(=O)OC1CC(C)(C)NC(C)(C)C1 SQRYDOGPOHDUKZ-UHFFFAOYSA-N 0.000 description 1
- GUGVZCUAAGOTEU-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) 2-phenoxyacetate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)COC1=CC=CC=C1 GUGVZCUAAGOTEU-UHFFFAOYSA-N 0.000 description 1
- GGISPEWAEPDJDE-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) 2-phenylacetate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CC1=CC=CC=C1 GGISPEWAEPDJDE-UHFFFAOYSA-N 0.000 description 1
- XLUFLEGPJWJROM-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) 4-chlorobenzoate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)C1=CC=C(Cl)C=C1 XLUFLEGPJWJROM-UHFFFAOYSA-N 0.000 description 1
- GKXUSMDHTROIQZ-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OC1CC(C)(C)NC(C)(C)C1 GKXUSMDHTROIQZ-UHFFFAOYSA-N 0.000 description 1
- OKRSVCKJPLEHEY-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) acetate Chemical compound CC(=O)OC1CC(C)(C)NC(C)(C)C1 OKRSVCKJPLEHEY-UHFFFAOYSA-N 0.000 description 1
- JQIKKXAVQCNADX-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) benzenesulfinate Chemical compound C1C(C)(C)NC(C)(C)CC1OS(=O)C1=CC=CC=C1 JQIKKXAVQCNADX-UHFFFAOYSA-N 0.000 description 1
- NUSVTOLZLIGSSV-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) benzenesulfonate Chemical compound C1C(C)(C)NC(C)(C)CC1OS(=O)(=O)C1=CC=CC=C1 NUSVTOLZLIGSSV-UHFFFAOYSA-N 0.000 description 1
- YEYCMBWKTZNPDH-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) benzoate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)C1=CC=CC=C1 YEYCMBWKTZNPDH-UHFFFAOYSA-N 0.000 description 1
- JCAMPEQCOPAWBA-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) cyclohexanecarboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)C1CCCCC1 JCAMPEQCOPAWBA-UHFFFAOYSA-N 0.000 description 1
- MDKXPTZQZUEFJX-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) methanesulfonate Chemical compound CC1(C)CC(OS(C)(=O)=O)CC(C)(C)N1 MDKXPTZQZUEFJX-UHFFFAOYSA-N 0.000 description 1
- HWCSHANEIJRMQF-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) n-(2-methylphenyl)carbamate Chemical compound CC1=CC=CC=C1NC(=O)OC1CC(C)(C)NC(C)(C)C1 HWCSHANEIJRMQF-UHFFFAOYSA-N 0.000 description 1
- FJSFJBXBAYWSGB-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) n-(4-chlorophenyl)carbamate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)NC1=CC=C(Cl)C=C1 FJSFJBXBAYWSGB-UHFFFAOYSA-N 0.000 description 1
- KPQYTXOCFDUOQL-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) n-cyclohexylcarbamate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)NC1CCCCC1 KPQYTXOCFDUOQL-UHFFFAOYSA-N 0.000 description 1
- MCZHQCYHICIWJK-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) n-ethylcarbamate Chemical compound CCNC(=O)OC1CC(C)(C)NC(C)(C)C1 MCZHQCYHICIWJK-UHFFFAOYSA-N 0.000 description 1
- BRLBMLGYQWTHOH-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) n-naphthalen-1-ylcarbamate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)NC1=CC=CC2=CC=CC=C12 BRLBMLGYQWTHOH-UHFFFAOYSA-N 0.000 description 1
- GSTKDOVQEARANU-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) n-phenylcarbamate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)NC1=CC=CC=C1 GSTKDOVQEARANU-UHFFFAOYSA-N 0.000 description 1
- YCPUINYTTZGMGT-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) naphthalene-2-carboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)C1=CC=C(C=CC=C2)C2=C1 YCPUINYTTZGMGT-UHFFFAOYSA-N 0.000 description 1
- JMUOXOJMXILBTE-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 JMUOXOJMXILBTE-UHFFFAOYSA-N 0.000 description 1
- BUFCQVRLKYIQJP-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) prop-2-enoate Chemical compound CC1(C)CC(OC(=O)C=C)CC(C)(C)N1 BUFCQVRLKYIQJP-UHFFFAOYSA-N 0.000 description 1
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 1
- XQMHLQCMMWBAPP-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-[2-(2,2,6,6-tetramethylpiperidin-4-yl)oxyethoxy]piperidine Chemical compound C1C(C)(C)NC(C)(C)CC1OCCOC1CC(C)(C)NC(C)(C)C1 XQMHLQCMMWBAPP-UHFFFAOYSA-N 0.000 description 1
- BWJKLDGAAPQXGO-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-octadecoxypiperidine Chemical compound CCCCCCCCCCCCCCCCCCOC1CC(C)(C)NC(C)(C)C1 BWJKLDGAAPQXGO-UHFFFAOYSA-N 0.000 description 1
- IUKIOUVQRQCBOX-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-phenoxypiperidine Chemical compound C1C(C)(C)NC(C)(C)CC1OC1=CC=CC=C1 IUKIOUVQRQCBOX-UHFFFAOYSA-N 0.000 description 1
- WDYYJEFALNLPOT-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-phenylmethoxypiperidine Chemical compound C1C(C)(C)NC(C)(C)CC1OCC1=CC=CC=C1 WDYYJEFALNLPOT-UHFFFAOYSA-N 0.000 description 1
- FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 1
- VDVUCLWJZJHFAV-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1 VDVUCLWJZJHFAV-UHFFFAOYSA-N 0.000 description 1
- AZOKEAVWRNFNHE-UHFFFAOYSA-N 4-cyclohexyloxy-2,2,6,6-tetramethylpiperidine Chemical compound C1C(C)(C)NC(C)(C)CC1OC1CCCCC1 AZOKEAVWRNFNHE-UHFFFAOYSA-N 0.000 description 1
- RWWGPCWSFFOXJN-UHFFFAOYSA-N 4-methoxy-2,2,6,6-tetramethylpiperidine Chemical compound COC1CC(C)(C)NC(C)(C)C1 RWWGPCWSFFOXJN-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229920006065 Leona® Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- SNOYIYKTIUXTEF-MDZDMXLPSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) (e)-but-2-enedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)\C=C\C(=O)OC1CC(C)(C)NC(C)(C)C1 SNOYIYKTIUXTEF-MDZDMXLPSA-N 0.000 description 1
- POBLEHWIWNSUCF-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) benzene-1,3-disulfonate Chemical compound C1C(C)(C)NC(C)(C)CC1OS(=O)(=O)C1=CC=CC(S(=O)(=O)OC2CC(C)(C)NC(C)(C)C2)=C1 POBLEHWIWNSUCF-UHFFFAOYSA-N 0.000 description 1
- GHJBIWHWRNKOFW-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) benzene-1,4-dicarboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)C1=CC=C(C(=O)OC2CC(C)(C)NC(C)(C)C2)C=C1 GHJBIWHWRNKOFW-UHFFFAOYSA-N 0.000 description 1
- VOTNCDKSGGSYMC-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) carbonate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)OC1CC(C)(C)NC(C)(C)C1 VOTNCDKSGGSYMC-UHFFFAOYSA-N 0.000 description 1
- URRNHWCYHDBVAT-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) cyclohexane-1,4-dicarboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)C1CCC(C(=O)OC2CC(C)(C)NC(C)(C)C2)CC1 URRNHWCYHDBVAT-UHFFFAOYSA-N 0.000 description 1
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 1
- UROGBLCMTWAODF-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) hexanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 UROGBLCMTWAODF-UHFFFAOYSA-N 0.000 description 1
- GMHDUYXGKJNFHH-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) oxalate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)C(=O)OC1CC(C)(C)NC(C)(C)C1 GMHDUYXGKJNFHH-UHFFFAOYSA-N 0.000 description 1
- DGBLGWVHPYOSAI-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) propanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CC(=O)OC1CC(C)(C)NC(C)(C)C1 DGBLGWVHPYOSAI-UHFFFAOYSA-N 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- DHIZQUGVHYGERJ-UHFFFAOYSA-N o-(2,2,6,6-tetramethylpiperidin-4-yl) n-cyclohexylcarbamothioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=S)NC1CCCCC1 DHIZQUGVHYGERJ-UHFFFAOYSA-N 0.000 description 1
- SCLDCPFXFSGQOV-UHFFFAOYSA-N o-(2,2,6,6-tetramethylpiperidin-4-yl) n-ethylcarbamothioate Chemical compound CCNC(=S)OC1CC(C)(C)NC(C)(C)C1 SCLDCPFXFSGQOV-UHFFFAOYSA-N 0.000 description 1
- PAGRTAOMGRRSPM-UHFFFAOYSA-N o-(2,2,6,6-tetramethylpiperidin-4-yl) n-phenylcarbamothioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=S)NC1=CC=CC=C1 PAGRTAOMGRRSPM-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003955 ε-lactams Chemical class 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7767882A JPS58194948A (ja) | 1982-05-10 | 1982-05-10 | ポリアミド樹脂組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7767882A JPS58194948A (ja) | 1982-05-10 | 1982-05-10 | ポリアミド樹脂組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58194948A JPS58194948A (ja) | 1983-11-14 |
| JPH0210183B2 true JPH0210183B2 (enrdf_load_stackoverflow) | 1990-03-07 |
Family
ID=13640543
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7767882A Granted JPS58194948A (ja) | 1982-05-10 | 1982-05-10 | ポリアミド樹脂組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58194948A (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2582385B2 (ja) * | 1987-12-11 | 1997-02-19 | 旭電化工業株式会社 | 安定化された合成樹脂組成物 |
-
1982
- 1982-05-10 JP JP7767882A patent/JPS58194948A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58194948A (ja) | 1983-11-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US8178628B2 (en) | Aliphatic polyester resin composition and method for production thereof | |
| CN114790330B (zh) | 一种阻燃性聚酰胺玻纤组合物及其制备方法 | |
| CA1039882A (en) | Moldable flameproofed polyamides | |
| US8232354B2 (en) | Method for producing a polylactic acid resin composition | |
| JPS6058463A (ja) | ポリフエニレンエ−テル樹脂とポリアミドの変性ブレンド | |
| JPS6150503B2 (enrdf_load_stackoverflow) | ||
| JP2020056003A (ja) | ポリアミド組成物及びその製造方法、並びに、成形品 | |
| JPS60168757A (ja) | 防火性ポリアミドを主体とする組成物 | |
| US4417021A (en) | Polyester composition and production thereof | |
| US5037869A (en) | Process for preparing flame retardant polyamide molding resins containing melamine cyanurate | |
| JPH0210183B2 (enrdf_load_stackoverflow) | ||
| JP6098058B2 (ja) | 難燃性ポリアミド樹脂組成物 | |
| JP2994207B2 (ja) | 非ハロゲン系の難燃性熱可塑性組成物 | |
| JPH0333134A (ja) | 難燃性ポリアミド樹脂成形物の製造法 | |
| JPS5915939B2 (ja) | 難燃性合成樹脂組成物 | |
| JPS62195043A (ja) | 難燃性ポリアミド樹脂組成物 | |
| JPWO2017212816A1 (ja) | 樹脂組成物 | |
| US4052360A (en) | Reinforced flame retardant polyester composition having non-drip characteristics | |
| JPS6149342B2 (enrdf_load_stackoverflow) | ||
| JPH0718179A (ja) | 難燃性ポリアミド樹脂組成物 | |
| JPH02248460A (ja) | 高結晶性ポリエステル樹脂組成物 | |
| JPH03131650A (ja) | 熱可塑性成形材料 | |
| JPS5841295B2 (ja) | 難燃性ポリアミド組成物の製造方法 | |
| JP3469267B2 (ja) | 難燃性ポリアミド樹脂組成物 | |
| JPH0138820B2 (enrdf_load_stackoverflow) |