JP2004034604A

JP2004034604A - 農業用フイルム

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Publication number: JP2004034604A
Authority: JP; Japan
Prior art keywords: group; weight; film; thermoplastic resin; layer
Prior art date: 2002-07-05
Legal status : Pending

Application number

JP2002197413A

Other languages

English (en)

Japanese (ja)

Other versions

JP2004034604A5 (enExample

Inventor

Tadashi Kimura

木村　正

Toshiyuki Maeda

前田　敏幸

Yoshiyuki Katayama

片山　義之

Current Assignee

Dow Mitsui Polychemicals Co Ltd

Original Assignee

Du Pont Mitsui Polychemicals Co Ltd

Priority date

2002-07-05

Filing date

2002-07-05

Publication date

2004-02-05

2002-07-05 Application filed by Du Pont Mitsui Polychemicals Co Ltd filed Critical Du Pont Mitsui Polychemicals Co Ltd

2002-07-05 Priority to JP2002197413A priority Critical patent/JP2004034604A/ja

2004-02-05 Publication of JP2004034604A publication Critical patent/JP2004034604A/ja

2005-09-29 Publication of JP2004034604A5 publication Critical patent/JP2004034604A5/ja

Status Pending legal-status Critical Current

Links

229920005992 thermoplastic resin Polymers 0.000 claims abstract description 35
239000003795 chemical substances by application Substances 0.000 claims abstract description 30
239000002131 composite material Substances 0.000 claims abstract description 25
239000004611 light stabiliser Substances 0.000 claims abstract description 12
239000006097 ultraviolet radiation absorber Substances 0.000 claims abstract description 12
150000002484 inorganic compounds Chemical class 0.000 claims abstract description 10
229910010272 inorganic material Inorganic materials 0.000 claims abstract description 10
239000011342 resin composition Substances 0.000 claims abstract description 10
239000002245 particle Substances 0.000 claims abstract description 9
GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 claims abstract description 8
229910052751 metal Inorganic materials 0.000 claims abstract description 6
239000002184 metal Substances 0.000 claims abstract description 6
150000002739 metals Chemical class 0.000 claims abstract description 6
229910052700 potassium Inorganic materials 0.000 claims abstract description 6
229910052782 aluminium Inorganic materials 0.000 claims abstract description 5
229920001577 copolymer Polymers 0.000 claims description 19
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 18
239000005977 Ethylene Substances 0.000 claims description 17
239000000654 additive Substances 0.000 claims description 13
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 8
230000000996 additive effect Effects 0.000 claims description 7
229920005672 polyolefin resin Polymers 0.000 claims description 7
239000003963 antioxidant agent Substances 0.000 claims description 5
239000000155 melt Substances 0.000 claims description 5
229920000642 polymer Polymers 0.000 claims description 4
230000003078 antioxidant effect Effects 0.000 claims description 3
239000000463 material Substances 0.000 claims description 3
239000002981 blocking agent Substances 0.000 claims description 2
239000006185 dispersion Substances 0.000 claims description 2
229920001038 ethylene copolymer Polymers 0.000 claims description 2
239000012748 slip agent Substances 0.000 claims description 2
239000003595 mist Substances 0.000 claims 1
238000010792 warming Methods 0.000 claims 1
238000002156 mixing Methods 0.000 abstract description 3
239000010410 layer Substances 0.000 description 76
-1 polyethylene Polymers 0.000 description 34
125000000217 alkyl group Chemical group 0.000 description 27
125000004432 carbon atom Chemical group C* 0.000 description 21
239000000203 mixture Substances 0.000 description 16
150000001875 compounds Chemical class 0.000 description 14
125000000753 cycloalkyl group Chemical group 0.000 description 14
235000014113 dietary fatty acids Nutrition 0.000 description 11
239000000194 fatty acid Substances 0.000 description 11
229930195729 fatty acid Natural products 0.000 description 11
125000002947 alkylene group Chemical group 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
239000003054 catalyst Substances 0.000 description 9
150000002431 hydrogen Chemical class 0.000 description 9
239000001257 hydrogen Substances 0.000 description 9
229910052739 hydrogen Inorganic materials 0.000 description 9
125000002252 acyl group Chemical group 0.000 description 7
125000002768 hydroxyalkyl group Chemical group 0.000 description 7
125000003710 aryl alkyl group Chemical group 0.000 description 6
229940125904 compound 1 Drugs 0.000 description 6
BITAPBDLHJQAID-KTKRTIGZSA-N 2-[2-hydroxyethyl-[(z)-octadec-9-enyl]amino]ethanol Chemical compound CCCCCCCC\C=C/CCCCCCCCN(CCO)CCO BITAPBDLHJQAID-KTKRTIGZSA-N 0.000 description 5
239000007983 Tris buffer Substances 0.000 description 5
239000002253 acid Substances 0.000 description 5
125000003342 alkenyl group Chemical group 0.000 description 5
125000003118 aryl group Chemical group 0.000 description 5
230000000052 comparative effect Effects 0.000 description 5
229940125782 compound 2 Drugs 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
229920000092 linear low density polyethylene Polymers 0.000 description 5
239000004707 linear low-density polyethylene Substances 0.000 description 5
229920001684 low density polyethylene Polymers 0.000 description 5
239000004702 low-density polyethylene Substances 0.000 description 5
239000000178 monomer Substances 0.000 description 5
229920005989 resin Polymers 0.000 description 5
239000011347 resin Substances 0.000 description 5
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 4
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 4
0 CC(*1*C(C)(C*)C=O)N1C(C)(C)CC(C)(C)*C1CC(C2(*3)C3CC2)(C=C)N(C)C(C)(*C*)C1 Chemical compound CC(*1*C(C)(C*)C=O)N1C(C)(C)CC(C)(C)*C1CC(C2(*3)C3CC2)(C=C)N(C)C(C)(*C*)C1 0.000 description 4
239000004698 Polyethylene Substances 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
238000009472 formulation Methods 0.000 description 4
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
230000000704 physical effect Effects 0.000 description 4
229920000573 polyethylene Polymers 0.000 description 4
150000005846 sugar alcohols Polymers 0.000 description 4
VJJGXHBNVRFKIQ-UHFFFAOYSA-N CC1(C)C(CCCC)C(OC(O)=O)CC(C)(C)N1OC(=O)C1=CC=CC=C1 Chemical compound CC1(C)C(CCCC)C(OC(O)=O)CC(C)(C)N1OC(=O)C1=CC=CC=C1 VJJGXHBNVRFKIQ-UHFFFAOYSA-N 0.000 description 3
101100389815 Caenorhabditis elegans eva-1 gene Proteins 0.000 description 3
235000021355 Stearic acid Nutrition 0.000 description 3
239000006096 absorbing agent Substances 0.000 description 3
229910052783 alkali metal Inorganic materials 0.000 description 3
150000001336 alkenes Chemical class 0.000 description 3
125000004183 alkoxy alkyl group Chemical group 0.000 description 3
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 3
125000000732 arylene group Chemical group 0.000 description 3
239000002585 base Substances 0.000 description 3
239000005038 ethylene vinyl acetate Substances 0.000 description 3
238000004898 kneading Methods 0.000 description 3
239000011777 magnesium Substances 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 3
239000008188 pellet Substances 0.000 description 3
230000002688 persistence Effects 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
229920003023 plastic Polymers 0.000 description 3
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
239000002356 single layer Substances 0.000 description 3
229910052708 sodium Inorganic materials 0.000 description 3
239000011734 sodium Substances 0.000 description 3
239000008117 stearic acid Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
230000002087 whitening effect Effects 0.000 description 3
239000004711 α-olefin Substances 0.000 description 3
DCERHXAVMTXRRA-UHFFFAOYSA-N (1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) octadecanoate Chemical compound CC1(C)CC(OC(=O)CCCCCCCCCCCCCCCCC)CC(C)(C)N1OC1CCCCC1 DCERHXAVMTXRRA-UHFFFAOYSA-N 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
JUDPCSIYBAFSNE-UHFFFAOYSA-N 1-ethoxy-2,2,6,6-tetramethyl-4-phenylmethoxypiperidine Chemical compound C1C(C)(C)N(OCC)C(C)(C)CC1OCC1=CC=CC=C1 JUDPCSIYBAFSNE-UHFFFAOYSA-N 0.000 description 2
PVHDGURUYLBNHN-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1,4-bis(phenylmethoxy)piperidine Chemical compound CC1(C)CC(OCC=2C=CC=CC=2)CC(C)(C)N1OCC1=CC=CC=C1 PVHDGURUYLBNHN-UHFFFAOYSA-N 0.000 description 2
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
WEWNSQLXBXCOQC-UHFFFAOYSA-N CC(C(=O)OC1CC(N(C(C1)(C)C)OC(NCCCC)=O)(C)C)(C(=O)OC1CC(N(C(C1)(C)C)OC(NCCCC)=O)(C)C)C Chemical compound CC(C(=O)OC1CC(N(C(C1)(C)C)OC(NCCCC)=O)(C)C)(C(=O)OC1CC(N(C(C1)(C)C)OC(NCCCC)=O)(C)C)C WEWNSQLXBXCOQC-UHFFFAOYSA-N 0.000 description 2
CHHSXJUAGIPPSX-UHFFFAOYSA-N CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(C(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)=C1 Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(C(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)=C1 CHHSXJUAGIPPSX-UHFFFAOYSA-N 0.000 description 2
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical group [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
235000021314 Palmitic acid Nutrition 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
PIMJKCTVTRETIR-UHFFFAOYSA-N [1-(3,5-ditert-butyl-4-hydroxybenzoyl)oxy-2,2,6,6-tetramethylpiperidin-4-yl] 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(C(=O)OC2CC(C)(C)N(OC(=O)C=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C(C)(C)C2)=C1 PIMJKCTVTRETIR-UHFFFAOYSA-N 0.000 description 2
LFJNTTKONDCMAF-UHFFFAOYSA-N [1-[[6-[(4-benzoyloxy-2,2,6,6-tetramethylpiperidin-1-yl)oxycarbonylamino]-3,3,5-trimethylhexyl]carbamoyloxy]-2,2,6,6-tetramethylpiperidin-4-yl] benzoate Chemical compound CC1(C)CC(OC(=O)C=2C=CC=CC=2)CC(C)(C)N1OC(=O)NCCC(C)(C)CC(C)CNC(=O)ON(C(C1)(C)C)C(C)(C)CC1OC(=O)C1=CC=CC=C1 LFJNTTKONDCMAF-UHFFFAOYSA-N 0.000 description 2
CNYMZKXROROLLW-UHFFFAOYSA-N [2,2,6,6-tetramethyl-1-(1-phenylethoxy)piperidin-4-yl] benzoate Chemical compound C=1C=CC=CC=1C(C)ON(C(C1)(C)C)C(C)(C)CC1OC(=O)C1=CC=CC=C1 CNYMZKXROROLLW-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
150000001340 alkali metals Chemical class 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 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
ZGRCDFPVLTXMGX-UHFFFAOYSA-N bis(1-benzoyloxy-2,2,6,6-tetramethylpiperidin-4-yl) benzene-1,2-dicarboxylate Chemical compound CC1(C)CC(OC(=O)C=2C(=CC=CC=2)C(=O)OC2CC(C)(C)N(OC(=O)C=3C=CC=CC=3)C(C)(C)C2)CC(C)(C)N1OC(=O)C1=CC=CC=C1 ZGRCDFPVLTXMGX-UHFFFAOYSA-N 0.000 description 2
NTPZJLAVYDXWAL-UHFFFAOYSA-N bis(1-benzoyloxy-2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound CC1(C)CC(OC(=O)CCCCCCCCC(=O)OC2CC(C)(C)N(OC(=O)C=3C=CC=CC=3)C(C)(C)C2)CC(C)(C)N1OC(=O)C1=CC=CC=C1 NTPZJLAVYDXWAL-UHFFFAOYSA-N 0.000 description 2
AABWVAVHNGUOML-UHFFFAOYSA-N bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) benzene-1,2-dicarboxylate Chemical compound CC1(C)CC(OC(=O)C=2C(=CC=CC=2)C(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1 AABWVAVHNGUOML-UHFFFAOYSA-N 0.000 description 2
WYYIPIRNYXXARB-UHFFFAOYSA-N bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) benzene-1,3-dicarboxylate Chemical compound CC1(C)CC(OC(=O)C=2C=C(C=CC=2)C(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1 WYYIPIRNYXXARB-UHFFFAOYSA-N 0.000 description 2
UXIVRFXHQNHKCC-UHFFFAOYSA-N bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) butanedioate Chemical compound CC1(C)CC(OC(=O)CCC(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1 UXIVRFXHQNHKCC-UHFFFAOYSA-N 0.000 description 2
DLHNOZQXRABONJ-UHFFFAOYSA-N bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound CC1(C)CC(OC(=O)CCCCCCCCC(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1 DLHNOZQXRABONJ-UHFFFAOYSA-N 0.000 description 2
JLOAPAGFWFMZLD-UHFFFAOYSA-N bis(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl) hexanedioate Chemical compound CC1(C)CC(OC(=O)CCCCC(=O)OC2CC(C)(C)N(OC3CCCCC3)C(C)(C)C2)CC(C)(C)N1OC1CCCCC1 JLOAPAGFWFMZLD-UHFFFAOYSA-N 0.000 description 2
PDXLZLIZLGEIBQ-UHFFFAOYSA-N bis(1-ethoxy-2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCC)C(C)(C)C1 PDXLZLIZLGEIBQ-UHFFFAOYSA-N 0.000 description 2
BFRZTRMJVRDRRD-UHFFFAOYSA-N bis(1-heptoxy-2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCC)C(C)(C)C1 BFRZTRMJVRDRRD-UHFFFAOYSA-N 0.000 description 2
JDLFYESLPIMSAN-UHFFFAOYSA-N bis(1-methoxy-2,2,6,6-tetramethylpiperidin-4-yl) butanedioate Chemical compound C1C(C)(C)N(OC)C(C)(C)CC1OC(=O)CCC(=O)OC1CC(C)(C)N(OC)C(C)(C)C1 JDLFYESLPIMSAN-UHFFFAOYSA-N 0.000 description 2
XGJSMYFOSRLZNF-UHFFFAOYSA-N bis(1-methoxy-2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OC)C(C)(C)C1 XGJSMYFOSRLZNF-UHFFFAOYSA-N 0.000 description 2
JKAYBCSFEXXXOF-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octadecoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCCCCCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCCCCCCCCCCCC)C(C)(C)C1 JKAYBCSFEXXXOF-UHFFFAOYSA-N 0.000 description 2
UTJYIWKQDSWNJU-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) butanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 UTJYIWKQDSWNJU-UHFFFAOYSA-N 0.000 description 2
OSIVCXJNIBEGCL-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 OSIVCXJNIBEGCL-UHFFFAOYSA-N 0.000 description 2
DBECPNDSMYQTJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-phenylmethoxypiperidin-4-yl) decanedioate Chemical compound CC1(C)CC(OC(=O)CCCCCCCCC(=O)OC2CC(C)(C)N(OCC=3C=CC=CC=3)C(C)(C)C2)CC(C)(C)N1OCC1=CC=CC=C1 DBECPNDSMYQTJN-UHFFFAOYSA-N 0.000 description 2
OUCXZAWAIJMEED-UHFFFAOYSA-N bis[1-(butylcarbamoyloxy)-2,2,6,6-tetramethylpiperidin-4-yl] benzene-1,2-dicarboxylate Chemical compound C1C(C)(C)N(OC(=O)NCCCC)C(C)(C)CC1OC(=O)C1=CC=CC=C1C(=O)OC1CC(C)(C)N(OC(=O)NCCCC)C(C)(C)C1 OUCXZAWAIJMEED-UHFFFAOYSA-N 0.000 description 2
QOWWCWMDZGAETE-UHFFFAOYSA-N bis[1-(butylcarbamoyloxy)-2,2,6,6-tetramethylpiperidin-4-yl] benzene-1,3-dicarboxylate Chemical compound C1C(C)(C)N(OC(=O)NCCCC)C(C)(C)CC1OC(=O)C1=CC=CC(C(=O)OC2CC(C)(C)N(OC(=O)NCCCC)C(C)(C)C2)=C1 QOWWCWMDZGAETE-UHFFFAOYSA-N 0.000 description 2
QTTUNKMWOFLWJP-UHFFFAOYSA-N bis[2,2,6,6-tetramethyl-1-(1-phenylethoxy)piperidin-4-yl] benzene-1,3-dicarboxylate Chemical compound C=1C=CC=CC=1C(C)ON(C(C1)(C)C)C(C)(C)CC1OC(=O)C(C=1)=CC=CC=1C(=O)OC(CC1(C)C)CC(C)(C)N1OC(C)C1=CC=CC=C1 QTTUNKMWOFLWJP-UHFFFAOYSA-N 0.000 description 2
CCGJODYDJUXXEI-UHFFFAOYSA-N bis[2,2,6,6-tetramethyl-1-(1-phenylethoxy)piperidin-4-yl] benzene-1,4-dicarboxylate Chemical compound C=1C=CC=CC=1C(C)ON(C(C1)(C)C)C(C)(C)CC1OC(=O)C(C=C1)=CC=C1C(=O)OC(CC1(C)C)CC(C)(C)N1OC(C)C1=CC=CC=C1 CCGJODYDJUXXEI-UHFFFAOYSA-N 0.000 description 2
CKNOOCGHEOYBCQ-UHFFFAOYSA-N bis[2,2,6,6-tetramethyl-1-(2-phenylpropan-2-yloxy)piperidin-4-yl] decanedioate Chemical compound C=1C=CC=CC=1C(C)(C)ON(C(C1)(C)C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC(CC1(C)C)CC(C)(C)N1OC(C)(C)C1=CC=CC=C1 CKNOOCGHEOYBCQ-UHFFFAOYSA-N 0.000 description 2
OCWYEMOEOGEQAN-UHFFFAOYSA-N bumetrizole Chemical compound CC(C)(C)C1=CC(C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O OCWYEMOEOGEQAN-UHFFFAOYSA-N 0.000 description 2
150000007942 carboxylates Chemical group 0.000 description 2
238000013329 compounding Methods 0.000 description 2
229940105990 diglycerin Drugs 0.000 description 2
GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
125000001841 imino group Chemical group [H]N=* 0.000 description 2
229910052744 lithium Inorganic materials 0.000 description 2
XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 2
229910052808 lithium carbonate Inorganic materials 0.000 description 2
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