AU2008202150B2 - Use of UV absorbers in the production of transparent polyamide molded parts - Google Patents
Use of UV absorbers in the production of transparent polyamide molded parts Download PDFInfo
- Publication number
- AU2008202150B2 AU2008202150B2 AU2008202150A AU2008202150A AU2008202150B2 AU 2008202150 B2 AU2008202150 B2 AU 2008202150B2 AU 2008202150 A AU2008202150 A AU 2008202150A AU 2008202150 A AU2008202150 A AU 2008202150A AU 2008202150 B2 AU2008202150 B2 AU 2008202150B2
- Authority
- AU
- Australia
- Prior art keywords
- acid
- polyamide
- absorber
- extrusion molding
- molding compound
- 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.)
- Ceased
Links
- 239000004952 Polyamide Substances 0.000 title claims abstract description 168
- 229920002647 polyamide Polymers 0.000 title claims abstract description 168
- 239000006096 absorbing agent Substances 0.000 title claims abstract description 132
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 18
- 150000001875 compounds Chemical class 0.000 claims abstract description 53
- -1 dibenzoylmethane compound Chemical class 0.000 claims abstract description 26
- 238000012545 processing Methods 0.000 claims abstract description 16
- 239000000155 melt Substances 0.000 claims abstract description 12
- 230000005540 biological transmission Effects 0.000 claims description 60
- 238000001746 injection moulding Methods 0.000 claims description 34
- 239000007924 injection Substances 0.000 claims description 31
- 238000001125 extrusion Methods 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims description 18
- BNJOQKFENDDGSC-UHFFFAOYSA-N octadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCC(O)=O BNJOQKFENDDGSC-UHFFFAOYSA-N 0.000 claims description 12
- HQHCYKULIHKCEB-UHFFFAOYSA-N tetradecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCC(O)=O HQHCYKULIHKCEB-UHFFFAOYSA-N 0.000 claims description 12
- 229920003023 plastic Polymers 0.000 claims description 11
- BTZVDPWKGXMQFW-UHFFFAOYSA-N Pentadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCC(O)=O BTZVDPWKGXMQFW-UHFFFAOYSA-N 0.000 claims description 10
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 10
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 10
- QQHJDPROMQRDLA-UHFFFAOYSA-N hexadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCC(O)=O QQHJDPROMQRDLA-UHFFFAOYSA-N 0.000 claims description 10
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 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 10
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 10
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical class C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 claims description 9
- 238000002347 injection Methods 0.000 claims description 9
- 150000004985 diamines Chemical class 0.000 claims description 8
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 7
- XNEFYCZVKIDDMS-UHFFFAOYSA-N avobenzone Chemical compound C1=CC(OC)=CC=C1C(=O)CC(=O)C1=CC=C(C(C)(C)C)C=C1 XNEFYCZVKIDDMS-UHFFFAOYSA-N 0.000 claims description 7
- 150000003951 lactams Chemical class 0.000 claims description 7
- 239000004033 plastic Substances 0.000 claims description 7
- QCNWZROVPSVEJA-UHFFFAOYSA-N Heptadecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCC(O)=O QCNWZROVPSVEJA-UHFFFAOYSA-N 0.000 claims description 6
- 229920000572 Nylon 6/12 Polymers 0.000 claims description 6
- 239000000975 dye Substances 0.000 claims description 6
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 claims description 6
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 claims description 6
- LWBHHRRTOZQPDM-UHFFFAOYSA-N undecanedioic acid Chemical compound OC(=O)CCCCCCCCCC(O)=O LWBHHRRTOZQPDM-UHFFFAOYSA-N 0.000 claims description 6
- 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 claims description 5
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 claims description 5
- GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 claims description 5
- 239000001361 adipic acid Substances 0.000 claims description 5
- 235000011037 adipic acid Nutrition 0.000 claims description 5
- XMSVKICKONKVNM-UHFFFAOYSA-N bicyclo[2.2.1]heptane-3,4-diamine Chemical compound C1CC2(N)C(N)CC1C2 XMSVKICKONKVNM-UHFFFAOYSA-N 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- FDATWRLUYRHCJE-UHFFFAOYSA-N diethylamino hydroxybenzoyl hexyl benzoate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1C(=O)C1=CC=C(N(CC)CC)C=C1O FDATWRLUYRHCJE-UHFFFAOYSA-N 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 230000003287 optical effect Effects 0.000 claims description 5
- 229920006114 semi-crystalline semi-aromatic polyamide Polymers 0.000 claims description 5
- DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 claims description 5
- ZCILGMFPJBRCNO-UHFFFAOYSA-N 4-phenyl-2H-benzotriazol-5-ol Chemical class OC1=CC=C2NN=NC2=C1C1=CC=CC=C1 ZCILGMFPJBRCNO-UHFFFAOYSA-N 0.000 claims description 4
- 101000576320 Homo sapiens Max-binding protein MNT Proteins 0.000 claims description 4
- 229920006121 Polyxylylene adipamide Polymers 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- JJOJFIHJIRWASH-UHFFFAOYSA-N icosanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCCCC(O)=O JJOJFIHJIRWASH-UHFFFAOYSA-N 0.000 claims description 4
- ZETYUTMSJWMKNQ-UHFFFAOYSA-N n,n',n'-trimethylhexane-1,6-diamine Chemical compound CNCCCCCCN(C)C ZETYUTMSJWMKNQ-UHFFFAOYSA-N 0.000 claims description 4
- 230000001681 protective effect Effects 0.000 claims description 4
- SPJXZYLLLWOSLQ-UHFFFAOYSA-N 1-[(1-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CCCCC1(N)CC1(N)CCCCC1 SPJXZYLLLWOSLQ-UHFFFAOYSA-N 0.000 claims description 3
- AXCGJDULNLWQKB-UHFFFAOYSA-N 1-[2-(1-aminocyclohexyl)propan-2-yl]cyclohexan-1-amine Chemical compound C1CCCCC1(N)C(C)(C)C1(N)CCCCC1 AXCGJDULNLWQKB-UHFFFAOYSA-N 0.000 claims description 3
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 3
- QFGCFKJIPBRJGM-UHFFFAOYSA-N 12-[(2-methylpropan-2-yl)oxy]-12-oxododecanoic acid Chemical compound CC(C)(C)OC(=O)CCCCCCCCCCC(O)=O QFGCFKJIPBRJGM-UHFFFAOYSA-N 0.000 claims description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 3
- PWLXTFFHCFWCGG-UHFFFAOYSA-N Heneicosanedioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCCCCC(O)=O PWLXTFFHCFWCGG-UHFFFAOYSA-N 0.000 claims description 3
- UUGLJVMIFJNVFH-UHFFFAOYSA-N Hexyl benzoate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1 UUGLJVMIFJNVFH-UHFFFAOYSA-N 0.000 claims description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 3
- IFAWYXIHOVRGHQ-UHFFFAOYSA-N Nonadecandioic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCCC(O)=O IFAWYXIHOVRGHQ-UHFFFAOYSA-N 0.000 claims description 3
- 229920000571 Nylon 11 Polymers 0.000 claims description 3
- 229920000299 Nylon 12 Polymers 0.000 claims description 3
- 229920002614 Polyether block amide Polymers 0.000 claims description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 3
- XZAHJRZBUWYCBM-UHFFFAOYSA-N [1-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1(CN)CCCCC1 XZAHJRZBUWYCBM-UHFFFAOYSA-N 0.000 claims description 3
- RPYFJVIASOJLJS-UHFFFAOYSA-N [3-(aminomethyl)-2-bicyclo[2.2.1]heptanyl]methanamine Chemical compound C1CC2C(CN)C(CN)C1C2 RPYFJVIASOJLJS-UHFFFAOYSA-N 0.000 claims description 3
- 150000001413 amino acids Chemical class 0.000 claims description 3
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 3
- 239000001000 anthraquinone dye Substances 0.000 claims description 3
- QVYARBLCAHCSFJ-UHFFFAOYSA-N butane-1,1-diamine Chemical compound CCCC(N)N QVYARBLCAHCSFJ-UHFFFAOYSA-N 0.000 claims description 3
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 3
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 claims description 3
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 3
- 239000011521 glass Substances 0.000 claims description 3
- NWOJEYNEKIVOOF-UHFFFAOYSA-N hexane-2,2-diamine Chemical compound CCCCC(C)(N)N NWOJEYNEKIVOOF-UHFFFAOYSA-N 0.000 claims description 3
- 229920006146 polyetheresteramide block copolymer Polymers 0.000 claims description 3
- JZUHIOJYCPIVLQ-UHFFFAOYSA-N 2-methylpentane-1,5-diamine Chemical compound NCC(C)CCCN JZUHIOJYCPIVLQ-UHFFFAOYSA-N 0.000 claims 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 claims description 2
- 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 claims description 2
- DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 claims description 2
- MFYOOJRJTYUYHL-UHFFFAOYSA-N 4-amino-2-benzoyl-3-hydroxybenzoic acid Chemical class NC1=CC=C(C(O)=O)C(C(=O)C=2C=CC=CC=2)=C1O MFYOOJRJTYUYHL-UHFFFAOYSA-N 0.000 claims description 2
- 229920000305 Nylon 6,10 Polymers 0.000 claims description 2
- 229920006143 PA616 Polymers 0.000 claims description 2
- 229920006144 PA618 Polymers 0.000 claims description 2
- QLBRROYTTDFLDX-UHFFFAOYSA-N [3-(aminomethyl)cyclohexyl]methanamine Chemical compound NCC1CCCC(CN)C1 QLBRROYTTDFLDX-UHFFFAOYSA-N 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- XBZSBBLNHFMTEB-UHFFFAOYSA-N cyclohexane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCCC(C(O)=O)C1 XBZSBBLNHFMTEB-UHFFFAOYSA-N 0.000 claims description 2
- TVIDDXQYHWJXFK-UHFFFAOYSA-N n-Dodecanedioic acid Natural products OC(=O)CCCCCCCCCCC(O)=O TVIDDXQYHWJXFK-UHFFFAOYSA-N 0.000 claims description 2
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 claims description 2
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 claims 1
- 238000000465 moulding Methods 0.000 abstract description 34
- 229920006110 poly(m-benzoyl4,4'-methylenebis(cyclohexylamine)) Polymers 0.000 abstract description 8
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract description 6
- 238000012360 testing method Methods 0.000 description 79
- 230000000052 comparative effect Effects 0.000 description 22
- 239000003795 chemical substances by application Substances 0.000 description 10
- 239000004594 Masterbatch (MB) Substances 0.000 description 8
- 239000008187 granular material Substances 0.000 description 7
- 230000006750 UV protection Effects 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000002542 deteriorative effect Effects 0.000 description 4
- 150000001991 dicarboxylic acids Chemical class 0.000 description 4
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 238000004383 yellowing Methods 0.000 description 4
- 238000013329 compounding Methods 0.000 description 3
- 230000009477 glass transition Effects 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 229940116353 sebacic acid Drugs 0.000 description 3
- IBABXJRXGSAJLQ-UHFFFAOYSA-N 1,4-bis(2,6-diethyl-4-methylanilino)anthracene-9,10-dione Chemical compound CCC1=CC(C)=CC(CC)=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=C(CC)C=C(C)C=C1CC IBABXJRXGSAJLQ-UHFFFAOYSA-N 0.000 description 2
- 239000012963 UV stabilizer Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
- 239000012964 benzotriazole Substances 0.000 description 2
- 238000007872 degassing Methods 0.000 description 2
- 238000000113 differential scanning calorimetry Methods 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- VUJGKADZTYCLIL-YHPRVSEPSA-L disodium;5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfonatophenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].C=1C=C(\C=C\C=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S([O-])(=O)=O)C(S(=O)(=O)[O-])=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 VUJGKADZTYCLIL-YHPRVSEPSA-L 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920006123 polyhexamethylene isophthalamide Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- GUOSQNAUYHMCRU-UHFFFAOYSA-N 11-Aminoundecanoic acid Chemical compound NCCCCCCCCCCC(O)=O GUOSQNAUYHMCRU-UHFFFAOYSA-N 0.000 description 1
- VJHDPVWEDUCKRQ-UHFFFAOYSA-N 12-aminododecanoic acid Chemical compound NCCCCCCCCCCCC(O)=O.NCCCCCCCCCCCC(O)=O VJHDPVWEDUCKRQ-UHFFFAOYSA-N 0.000 description 1
- HWRLEEPNFJNTOP-UHFFFAOYSA-N 2-(1,3,5-triazin-2-yl)phenol Chemical compound OC1=CC=CC=C1C1=NC=NC=N1 HWRLEEPNFJNTOP-UHFFFAOYSA-N 0.000 description 1
- OLFNXLXEGXRUOI-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-bis(2-phenylpropan-2-yl)phenol Chemical compound C=1C(N2N=C3C=CC=CC3=N2)=C(O)C(C(C)(C)C=2C=CC=CC=2)=CC=1C(C)(C)C1=CC=CC=C1 OLFNXLXEGXRUOI-UHFFFAOYSA-N 0.000 description 1
- BWSQKOKULIALEW-UHFFFAOYSA-N 2-[2-[4-fluoro-3-(trifluoromethyl)phenyl]-3-[2-(piperidin-3-ylamino)pyrimidin-4-yl]imidazol-4-yl]acetonitrile Chemical compound FC1=C(C=C(C=C1)C=1N(C(=CN=1)CC#N)C1=NC(=NC=C1)NC1CNCCC1)C(F)(F)F BWSQKOKULIALEW-UHFFFAOYSA-N 0.000 description 1
- DWKNOLCXIFYNFV-HSZRJFAPSA-N 2-[[(2r)-1-[1-[(4-chloro-3-methylphenyl)methyl]piperidin-4-yl]-5-oxopyrrolidine-2-carbonyl]amino]-n,n,6-trimethylpyridine-4-carboxamide Chemical compound CN(C)C(=O)C1=CC(C)=NC(NC(=O)[C@@H]2N(C(=O)CC2)C2CCN(CC=3C=C(C)C(Cl)=CC=3)CC2)=C1 DWKNOLCXIFYNFV-HSZRJFAPSA-N 0.000 description 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
- ICBZSKCTKKUQSY-YUWZRIFDSA-N 4-[(1r,2s)-1-hydroxy-2-(methylamino)propyl]phenol;hydrochloride Chemical compound Cl.CN[C@@H](C)[C@H](O)C1=CC=C(O)C=C1 ICBZSKCTKKUQSY-YUWZRIFDSA-N 0.000 description 1
- PGLFPEYYIQQJOP-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O.NCCCCCC(O)=O PGLFPEYYIQQJOP-UHFFFAOYSA-N 0.000 description 1
- XDOLZJYETYVRKV-UHFFFAOYSA-N 7-Aminoheptanoic acid Chemical compound NCCCCCCC(O)=O XDOLZJYETYVRKV-UHFFFAOYSA-N 0.000 description 1
- UQXNEWQGGVUVQA-UHFFFAOYSA-N 8-aminooctanoic acid Chemical compound NCCCCCCCC(O)=O UQXNEWQGGVUVQA-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241001131696 Eurystomus Species 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- 241000511976 Hoya Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 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
- 150000007513 acids Chemical class 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229960005193 avobenzone Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SYFOAKAXGNMQAX-UHFFFAOYSA-N bis(prop-2-enyl) carbonate;2-(2-hydroxyethoxy)ethanol Chemical compound OCCOCCO.C=CCOC(=O)OCC=C SYFOAKAXGNMQAX-UHFFFAOYSA-N 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000000748 compression moulding Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920006039 crystalline polyamide Polymers 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 229960003692 gamma aminobutyric acid Drugs 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000006082 mold release agent Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- PBLZLIFKVPJDCO-UHFFFAOYSA-N omega-Aminododecanoic acid Natural products NCCCCCCCCCCCC(O)=O PBLZLIFKVPJDCO-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 235000014786 phosphorus Nutrition 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 229920006131 poly(hexamethylene isophthalamide-co-terephthalamide) Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- QEMSHZOGUJXBQA-UHFFFAOYSA-N sulfanyl carbamate Chemical compound NC(=O)OS QEMSHZOGUJXBQA-UHFFFAOYSA-N 0.000 description 1
- 150000003553 thiiranes Chemical class 0.000 description 1
- JTQAPFZZCXWQNQ-UHFFFAOYSA-N thiirene Chemical compound S1C=C1 JTQAPFZZCXWQNQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/07—Aldehydes; Ketones
-
- 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3472—Five-membered rings
- C08K5/3475—Five-membered rings condensed with carbocyclic rings
-
- 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
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)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07108313.3 | 2007-05-16 | ||
| EP07108313.3A EP1992659B1 (de) | 2007-05-16 | 2007-05-16 | Polyamidformmassen-Schmelze zur Herstellung von transparenten Formteilen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2008202150A1 AU2008202150A1 (en) | 2008-12-04 |
| AU2008202150B2 true AU2008202150B2 (en) | 2013-06-20 |
Family
ID=38512182
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2008202150A Ceased AU2008202150B2 (en) | 2007-05-16 | 2008-05-15 | Use of UV absorbers in the production of transparent polyamide molded parts |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8138243B2 (enExample) |
| EP (1) | EP1992659B1 (enExample) |
| JP (1) | JP5241318B2 (enExample) |
| KR (1) | KR101521298B1 (enExample) |
| CN (1) | CN101328313B (enExample) |
| AU (1) | AU2008202150B2 (enExample) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9567444B2 (en) | 2010-03-17 | 2017-02-14 | Evonik Röhm Gmbh | Chemical-resistant films in high optical quality |
| BR112012026493A2 (pt) * | 2010-04-16 | 2016-08-16 | Dsm Ip Assets Bv | peças moldadas por injeção produzidas de uma composição polimérica compreendendo poliamida 410(pa-410) |
| WO2011138396A1 (en) * | 2010-05-06 | 2011-11-10 | Dsm Ip Assets B.V. | Process for the production of pa-410 and pa-410 obtainable by that process |
| JP5824777B2 (ja) * | 2010-06-23 | 2015-12-02 | ディーエスエム アイピー アセッツ ビー．ブイ． | フィルムまたはプレート |
| CN102959014B (zh) * | 2010-07-08 | 2014-08-27 | 三菱瓦斯化学株式会社 | 聚酰胺树脂组合物 |
| JP5729189B2 (ja) * | 2010-07-23 | 2015-06-03 | 三菱瓦斯化学株式会社 | ポリアミド樹脂組成物 |
| JP2013532747A (ja) * | 2010-07-26 | 2013-08-19 | ディーエスエム アイピー アセッツ ビー．ブイ． | 燃料部品および燃料部品の製造方法 |
| JP5696001B2 (ja) * | 2011-08-19 | 2015-04-08 | Hoya株式会社 | プラスチックレンズの製造方法 |
| US20130052384A1 (en) * | 2011-08-29 | 2013-02-28 | E I Du Pont De Nemours And Company | Copolyamide compositions derived from vegetable oil |
| JP6065496B2 (ja) * | 2012-09-25 | 2017-01-25 | Dic株式会社 | 光重合性組成物、その硬化物、及びプラスチックレンズシート |
| EP2927273B1 (de) | 2014-04-02 | 2017-06-07 | Ems-Patent Ag | Polyamidformmasse, hieraus hergestellte Formkörper sowie Verwendung der Polyamidformmassen |
| EP2957598A1 (de) * | 2014-06-20 | 2015-12-23 | Ems-Patent Ag | Komposit enthaltend ein matrixmaterial aus einem amorphen polyamid und dessen verwendung |
| CN104172562B (zh) * | 2014-08-01 | 2015-09-30 | 杭州形尚众至服饰有限公司 | 具有360°超弹力的无痕托腹裤的生产工艺 |
| EP3356881A4 (en) | 2015-09-29 | 2019-08-14 | Vision Ease LP | GLASSES FOR ABSORPTION OF UV AND HIGHERGETIC VISIBLE LIGHT |
| JP6917187B2 (ja) * | 2016-05-10 | 2021-08-11 | 住友化学株式会社 | 光学フィルム、及びこれを用いたフレキシブルデバイス |
| TWI773728B (zh) * | 2017-02-01 | 2022-08-11 | 日商住友化學股份有限公司 | 聚醯亞胺膜 |
| KR102316905B1 (ko) | 2017-03-10 | 2021-10-25 | 어드밴식스 레진즈 앤드 케미컬즈 엘엘씨 | 개선된 가공성 및 특성을 위한 pa6/66 공중합체 베이스 수지의 와이어 및 케이블 피복 조성물 |
| EP3444113B1 (de) * | 2017-08-18 | 2021-01-20 | Ems-Chemie Ag | Verstärkte polyamid-formmassen mit geringem haze und formkörper daraus |
| JP7308818B2 (ja) | 2017-09-28 | 2023-07-14 | デュポン ポリマーズ インコーポレイテッド | 重合方法 |
| US11155692B2 (en) * | 2017-12-18 | 2021-10-26 | Basf Se | Polyamide molding compositions with improved optical properties and use of colorants therein |
| EP3502189A1 (de) * | 2017-12-22 | 2019-06-26 | EMS-Patent AG | Verwendung einer polyamid-formmassen zur reduktion von belagsbildung bei der thermoplastischen verarbeitung, polyamid-formmasse und verfahren zur herstellung von gebrauchsgegenständen |
| EP3502164B1 (de) | 2017-12-22 | 2022-10-05 | Ems-Chemie Ag | Polyamid-formmasse |
| EP3502191B1 (de) | 2017-12-22 | 2021-02-17 | Ems-Chemie Ag | Polyamid-formmasse |
| KR102466771B1 (ko) * | 2018-11-02 | 2022-11-14 | 주식회사 엘지화학 | 편광판 |
| KR102318724B1 (ko) * | 2018-11-02 | 2021-10-28 | 주식회사 엘지화학 | 적층 필름 |
| US12031028B2 (en) | 2019-02-01 | 2024-07-09 | Lg Chem, Ltd. | Polyamide resin film and resin laminate using the same |
| KR20220139889A (ko) * | 2020-02-14 | 2022-10-17 | 미쯔비시 가스 케미칼 컴파니, 인코포레이티드 | 다층용기, 그의 제조방법, 및 재생폴리에스테르의 제조방법 |
| EP4227452A4 (en) * | 2020-10-08 | 2024-05-15 | Mitsubishi Gas Chemical Company, Inc. | Filament, material, and material manufacturing method |
| CN112480662A (zh) * | 2020-11-23 | 2021-03-12 | 山东广垠新材料有限公司 | 可吸收红外线透明尼龙及其制备方法 |
| JP7763224B2 (ja) * | 2023-11-16 | 2025-10-31 | ポリプラ・エボニック株式会社 | 偏光性積層体及び光学レンズ |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3248247A (en) * | 1961-06-16 | 1966-04-26 | Geigy Ag J R | Process for the stabilization of light sensitive resinous organic material and compositions prepared therefrom |
| US3826752A (en) * | 1970-03-11 | 1974-07-30 | Ciba Geigy Corp | Protective agents against light rays |
| US20020111330A1 (en) * | 2000-12-12 | 2002-08-15 | Carlos Pinzon | Compositions containing heteropolymers and methods of using same |
| WO2005025491A2 (en) * | 2003-09-04 | 2005-03-24 | Nalco Company | Water-soluble polyamioamides as sunscreen agents |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3988363A (en) * | 1973-09-25 | 1976-10-26 | Ciba-Geigy Corporation | 2,4,6-Trialkyl L-3-hydroxyphenylalkanoates |
| EP0610155A1 (en) * | 1993-02-04 | 1994-08-10 | Ciba-Geigy Ag | Stabilized polyamide compositions |
| DE4310970A1 (de) * | 1993-04-03 | 1994-10-06 | Huels Chemische Werke Ag | Farblose und transparente, amorph zu verarbeitende Polyamidformmassen mit guter Spannungsrißbeständigkeit und Schlagzähigkeit |
| US5500209A (en) * | 1994-03-17 | 1996-03-19 | The Mennen Company | Deodorant and antiperspirant compositions containing polyamide gelling agent |
| JP3354066B2 (ja) * | 1996-01-26 | 2002-12-09 | 帝人化成株式会社 | 眼鏡レンズ |
| US6277358B1 (en) * | 1997-12-15 | 2001-08-21 | Revlon Consumer Products Corporation | Cosmetic compositions containing crosslinkable polymers |
| US6592857B2 (en) * | 1999-01-04 | 2003-07-15 | Arizona Chemical Company | Tertiary amide terminated polyamides in cosmetics |
| US6855755B1 (en) * | 1999-08-04 | 2005-02-15 | Mitsubishi Engineering-Plastics Corporation | Polyamide resin composition having improved weathering resistance and its molded products |
| JP3676138B2 (ja) | 1999-09-20 | 2005-07-27 | Ｈｏｙａ株式会社 | 紫外線吸収性に優れたプラスチック眼鏡レンズ及びその製造方法 |
| JP3824455B2 (ja) | 1999-09-20 | 2006-09-20 | Ｈｏｙａ株式会社 | 紫外線吸収性に優れたプラスチック眼鏡レンズ及びその製造方法 |
| JP2003514805A (ja) * | 1999-11-16 | 2003-04-22 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | ベンゾトリアゾールｕｖ吸収剤の使用 |
| US6537670B1 (en) * | 2000-11-03 | 2003-03-25 | Cytec Technology Corp. | Bis(alkyleneoxybenzophenone) ultraviolet light absorbers |
| DE10122188B4 (de) * | 2001-05-08 | 2007-04-12 | Ems-Chemie Ag | Polyamidformmassen zur Herstellung optischer Linsen |
| JP2003019279A (ja) * | 2001-07-10 | 2003-01-21 | Maruhon Ind Co Ltd | 遊技機、プログラム、記録媒体 |
| JP2003192798A (ja) * | 2001-12-25 | 2003-07-09 | Toyobo Co Ltd | 透明ポリアミド系成形体 |
| EP1511802B1 (en) * | 2002-06-05 | 2010-09-08 | Showa Denko K.K. | Powder comprising silica-coated zinc oxide, organic polymer composition containing the powder and shaped article thereof |
| AU2003268631A1 (en) * | 2002-08-30 | 2004-04-30 | Toyo Boseki Kabushiki Kaisha | Method for continuous production of polyamide |
| DE10254548A1 (de) * | 2002-11-21 | 2004-06-17 | Basf Ag | Verwendung UV-Absorber enthaltender Polymerpulver zur Stabilisierung von Polymeren gegen die Einwirkung von UV-Strahlung |
| AU2003277903A1 (en) * | 2003-02-03 | 2004-08-30 | Dsm Ip Assets B.V. | Novel stabilized cinnamic ester sunscreen compositions |
| DE10308226A1 (de) * | 2003-02-25 | 2004-09-23 | Degussa Ag | Transparente Formmasse für optische Anwendungen |
| US20070190325A1 (en) * | 2003-12-04 | 2007-08-16 | Katja Berg-Schultz | Microcapsules with uv filter activity and process for producing them |
| DE102004032120A1 (de) * | 2004-07-01 | 2006-02-09 | Merck Patent Gmbh | Beugungsfarbmittel für die Kosmetik |
| JP5086802B2 (ja) * | 2005-02-17 | 2012-11-28 | 出光興産株式会社 | ４１０ｎｍの波長光に対して吸収能を持つ熱可塑性透明組成物およびその成形体 |
| CN101677938A (zh) * | 2007-04-05 | 2010-03-24 | 巴斯夫欧洲公司 | 包含无规三元共聚物的防晒组合物 |
-
2007
- 2007-05-16 EP EP07108313.3A patent/EP1992659B1/de active Active
-
2008
- 2008-05-15 AU AU2008202150A patent/AU2008202150B2/en not_active Ceased
- 2008-05-15 JP JP2008128547A patent/JP5241318B2/ja not_active Expired - Fee Related
- 2008-05-16 CN CN2008102103276A patent/CN101328313B/zh not_active Expired - Fee Related
- 2008-05-16 US US12/122,468 patent/US8138243B2/en active Active
- 2008-05-16 KR KR1020080045625A patent/KR101521298B1/ko not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3248247A (en) * | 1961-06-16 | 1966-04-26 | Geigy Ag J R | Process for the stabilization of light sensitive resinous organic material and compositions prepared therefrom |
| US3826752A (en) * | 1970-03-11 | 1974-07-30 | Ciba Geigy Corp | Protective agents against light rays |
| US20020111330A1 (en) * | 2000-12-12 | 2002-08-15 | Carlos Pinzon | Compositions containing heteropolymers and methods of using same |
| WO2005025491A2 (en) * | 2003-09-04 | 2005-03-24 | Nalco Company | Water-soluble polyamioamides as sunscreen agents |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2008202150A1 (en) | 2008-12-04 |
| KR20080101782A (ko) | 2008-11-21 |
| US8138243B2 (en) | 2012-03-20 |
| KR101521298B1 (ko) | 2015-05-18 |
| EP1992659A1 (de) | 2008-11-19 |
| JP2008303391A (ja) | 2008-12-18 |
| US20090085019A1 (en) | 2009-04-02 |
| EP1992659B1 (de) | 2016-07-20 |
| JP5241318B2 (ja) | 2013-07-17 |
| CN101328313A (zh) | 2008-12-24 |
| CN101328313B (zh) | 2012-07-18 |
| HK1122056A1 (en) | 2009-05-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AU2008202150B2 (en) | Use of UV absorbers in the production of transparent polyamide molded parts | |
| US6528560B2 (en) | Colorless, highly transparent polyamide blends with improved stress cracking resistance | |
| US4847356A (en) | Transparent copolyamide from bis(4-amino-3,5-diethyl cyclohexyl) methane | |
| KR102214746B1 (ko) | 비정질 코폴리아미드를 기반으로 하는 유리 필러-강화 폴리아미드 몰딩 컴파운드 | |
| AU2004200718B2 (en) | Transparent Molding Composition for Optical Applications | |
| KR20190019876A (ko) | 낮은 헤이즈를 가지는 보강 폴리아미드 성형 화합물 및 그로부터 제조된 성형체 | |
| MXPA03005052A (es) | Materiales de moldeo de poliamida transparente, que presentan una mejor transparencia resistencia a quimicos y alta resistencia a la fatiga permanente. | |
| DE3717928C2 (enExample) | ||
| EP2719726B1 (de) | Formmassen | |
| EP3502164B1 (de) | Polyamid-formmasse | |
| US6706790B1 (en) | Polyamide-based composition of high light stability | |
| US4232145A (en) | Injection moldable glass clear transparent polyamide | |
| US20210032465A1 (en) | Polyamide molding compound | |
| EP3502189A1 (de) | Verwendung einer polyamid-formmassen zur reduktion von belagsbildung bei der thermoplastischen verarbeitung, polyamid-formmasse und verfahren zur herstellung von gebrauchsgegenständen | |
| US4268661A (en) | Method for the manufacture of glass clear transparent polyamide | |
| US20030036625A1 (en) | Aromatic polyamide compositions for molding | |
| US12104055B2 (en) | Transparent polyamides with good weathering resistance | |
| CN116891631A (zh) | 具有高断裂强度的聚酰胺模塑材料及由其制备的模塑件 | |
| HK1122056B (en) | Use of uv absorbers in the production of transparent polyamide molded parts | |
| CA2449104A1 (en) | Method of making a polymer from a polymer precursor composition | |
| US20050113512A1 (en) | Method of making a polymer from a polymer precursor composition | |
| HK1126808A1 (en) | Photochrome moulding composition and objects made therefrom |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) | ||
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |