CN106479041B - 经改质的聚合物材料及复合式安定剂组成物 - Google Patents
经改质的聚合物材料及复合式安定剂组成物 Download PDFInfo
- Publication number
- CN106479041B CN106479041B CN201610674278.6A CN201610674278A CN106479041B CN 106479041 B CN106479041 B CN 106479041B CN 201610674278 A CN201610674278 A CN 201610674278A CN 106479041 B CN106479041 B CN 106479041B
- Authority
- CN
- China
- Prior art keywords
- chemical formula
- indicate
- alkyl
- aryl
- polymer material
- 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.)
- Active
Links
- 239000006084 composite stabilizer Substances 0.000 title abstract 4
- 239000000203 mixture Substances 0.000 title abstract 4
- 239000000463 material Substances 0.000 title description 9
- 239000000126 substance Substances 0.000 claims abstract description 56
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 55
- 239000002861 polymer material Substances 0.000 claims abstract description 35
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 33
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 22
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 22
- 239000011593 sulfur Substances 0.000 claims abstract description 22
- 150000007942 carboxylates Chemical class 0.000 claims abstract description 21
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 12
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000005977 Ethylene Substances 0.000 claims abstract description 7
- 229920001577 copolymer Polymers 0.000 claims abstract description 7
- 229920000098 polyolefin Polymers 0.000 claims abstract description 7
- 235000006708 antioxidants Nutrition 0.000 claims description 50
- 239000003795 chemical substances by application Substances 0.000 claims description 44
- -1 fatty acid salt Chemical class 0.000 claims description 33
- 239000000470 constituent Substances 0.000 claims description 31
- 230000006641 stabilisation Effects 0.000 claims description 30
- 238000011105 stabilization Methods 0.000 claims description 30
- 239000000758 substrate Substances 0.000 claims description 30
- 230000003647 oxidation Effects 0.000 claims description 17
- 238000007254 oxidation reaction Methods 0.000 claims description 17
- 230000001458 anti-acid effect Effects 0.000 claims description 14
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 claims description 13
- 239000004615 ingredient Substances 0.000 claims description 12
- 150000001412 amines Chemical class 0.000 claims description 10
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims description 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 238000012545 processing Methods 0.000 abstract description 16
- 238000000034 method Methods 0.000 abstract description 10
- 229920000307 polymer substrate Polymers 0.000 abstract description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052698 phosphorus Inorganic materials 0.000 abstract 1
- 239000011574 phosphorus Substances 0.000 abstract 1
- 238000001125 extrusion Methods 0.000 description 23
- 230000000052 comparative effect Effects 0.000 description 9
- 238000007493 shaping process Methods 0.000 description 9
- 239000004698 Polyethylene Substances 0.000 description 8
- 239000004743 Polypropylene Substances 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 229920001155 polypropylene Polymers 0.000 description 6
- 239000011575 calcium Substances 0.000 description 5
- BNAOQKULFPHAHL-UHFFFAOYSA-N 3,4-dibutyl-5-(2,4-dimethylphenyl)-3h-1-benzofuran-2-one Chemical compound CCCCC1=C2C(CCCC)C(=O)OC2=CC=C1C1=CC=C(C)C=C1C BNAOQKULFPHAHL-UHFFFAOYSA-N 0.000 description 3
- HCILJBJJZALOAL-UHFFFAOYSA-N 3-(3,5-ditert-butyl-4-hydroxyphenyl)-n'-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyl]propanehydrazide Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 HCILJBJJZALOAL-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 235000019260 propionic acid Nutrition 0.000 description 3
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- RGASRBUYZODJTG-UHFFFAOYSA-N 1,1-bis(2,4-ditert-butylphenyl)-2,2-bis(hydroxymethyl)propane-1,3-diol dihydroxyphosphanyl dihydrogen phosphite Chemical class OP(O)OP(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C(O)(C(CO)(CO)CO)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C RGASRBUYZODJTG-UHFFFAOYSA-N 0.000 description 2
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 2
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 2
- PZRWFKGUFWPFID-UHFFFAOYSA-N 3,9-dioctadecoxy-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane Chemical compound C1OP(OCCCCCCCCCCCCCCCCCC)OCC21COP(OCCCCCCCCCCCCCCCCCC)OC2 PZRWFKGUFWPFID-UHFFFAOYSA-N 0.000 description 2
- ZAAQJFLUOUQAOG-UHFFFAOYSA-N 4-benzyl-2,6-ditert-butylphenol Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CC=2C=CC=CC=2)=C1 ZAAQJFLUOUQAOG-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 235000013539 calcium stearate Nutrition 0.000 description 2
- 239000008116 calcium stearate Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000010525 oxidative degradation reaction Methods 0.000 description 2
- 238000005453 pelletization Methods 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 2
- IJRHDFLHUATAOS-DPMBMXLASA-M sodium ricinoleate Chemical compound [Na+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O IJRHDFLHUATAOS-DPMBMXLASA-M 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 2
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 description 1
- UNEATYXSUBPPKP-UHFFFAOYSA-N 1,3-Diisopropylbenzene Chemical compound CC(C)C1=CC=CC(C(C)C)=C1 UNEATYXSUBPPKP-UHFFFAOYSA-N 0.000 description 1
- QSRJVOOOWGXUDY-UHFFFAOYSA-N 2-[2-[2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]ethoxy]ethoxy]ethyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCCOCCOCCOC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 QSRJVOOOWGXUDY-UHFFFAOYSA-N 0.000 description 1
- OXWDLAHVJDUQJM-UHFFFAOYSA-N 2-[[2-[2-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]ethylamino]-2-oxoacetyl]amino]ethyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCCNC(=O)C(=O)NCCOC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 OXWDLAHVJDUQJM-UHFFFAOYSA-N 0.000 description 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-L 3-(2-carboxylatoethylsulfanyl)propanoate Chemical compound [O-]C(=O)CCSCCC([O-])=O ODJQKYXPKWQWNK-UHFFFAOYSA-L 0.000 description 1
- IZOFRDJGAYUGTP-UHFFFAOYSA-N 3-(3,5-ditert-butyl-2-hydroxyphenyl)-n'-[3-(3,5-ditert-butyl-2-hydroxyphenyl)propanoyl]propanehydrazide Chemical class CC(C)(C)C1=CC(C(C)(C)C)=CC(CCC(=O)NNC(=O)CCC=2C(=C(C=C(C=2)C(C)(C)C)C(C)(C)C)O)=C1O IZOFRDJGAYUGTP-UHFFFAOYSA-N 0.000 description 1
- UVRWBTOHALRHGR-UHFFFAOYSA-N 4-tert-butyl-2-(5-tert-butyl-1-benzofuran-3-yl)phenol Chemical compound CC(C)(C)C1=CC=C(O)C(C=2C3=CC(=CC=C3OC=2)C(C)(C)C)=C1 UVRWBTOHALRHGR-UHFFFAOYSA-N 0.000 description 1
- PKERXCMARBJNBX-UHFFFAOYSA-N 5-tert-butyl-3-(5-tert-butyl-2-hydroxyphenyl)-3h-1-benzofuran-2-one Chemical compound C12=CC(C(C)(C)C)=CC=C2OC(=O)C1C1=CC(C(C)(C)C)=CC=C1O PKERXCMARBJNBX-UHFFFAOYSA-N 0.000 description 1
- 206010004966 Bite Diseases 0.000 description 1
- XYXGHFLIABUDMF-UHFFFAOYSA-N CC(C)(C)C=1C(=C(C=C(C=1)C(C)(C)C)C1C(OC2=C1C=C(C=C2C(C)(C)C)C(C)(C)C)=O)O Chemical compound CC(C)(C)C=1C(=C(C=C(C=1)C(C)(C)C)C1C(OC2=C1C=C(C=C2C(C)(C)C)C(C)(C)C)=O)O XYXGHFLIABUDMF-UHFFFAOYSA-N 0.000 description 1
- NSMXENWDEWCHJS-UHFFFAOYSA-N CCCCCCCCCCCCCCCCCCC(CC(=O)S)O Chemical compound CCCCCCCCCCCCCCCCCCC(CC(=O)S)O NSMXENWDEWCHJS-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 241000790917 Dioxys <bee> Species 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- OKOBUGCCXMIKDM-UHFFFAOYSA-N Irganox 1098 Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)NCCCCCCNC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 OKOBUGCCXMIKDM-UHFFFAOYSA-N 0.000 description 1
- CFXCGWWYIDZIMU-UHFFFAOYSA-N Octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate Chemical compound CCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 CFXCGWWYIDZIMU-UHFFFAOYSA-N 0.000 description 1
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- AGJCRVTXPJSJGB-UHFFFAOYSA-N [Ca].C(CCCCCCCCCCC)C(CC(=S)O)O Chemical compound [Ca].C(CCCCCCCCCCC)C(CC(=S)O)O AGJCRVTXPJSJGB-UHFFFAOYSA-N 0.000 description 1
- CDBZCXRMRWVNDW-UHFFFAOYSA-N [Zn].C(CCCCCCCCCCC)C(CC(=S)O)O Chemical compound [Zn].C(CCCCCCCCCCC)C(CC(=S)O)O CDBZCXRMRWVNDW-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- DWSWCPPGLRSPIT-UHFFFAOYSA-N benzo[c][2,1]benzoxaphosphinin-6-ium 6-oxide Chemical compound C1=CC=C2[P+](=O)OC3=CC=CC=C3C2=C1 DWSWCPPGLRSPIT-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZPFKRQXYKULZKP-UHFFFAOYSA-N butylidene Chemical group [CH2+]CC[CH-] ZPFKRQXYKULZKP-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 1
- ZMOXKCINJLBMGB-UHFFFAOYSA-N docosanoic acid;magnesium Chemical compound [Mg].CCCCCCCCCCCCCCCCCCCCCC(O)=O ZMOXKCINJLBMGB-UHFFFAOYSA-N 0.000 description 1
- 229940000406 drug candidate Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003777 experimental drug Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 125000004464 hydroxyphenyl group Chemical group 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000005172 methylbenzenes Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- ITUWQZXQRZLLCR-UHFFFAOYSA-N n,n-dioctadecylhydroxylamine Chemical class CCCCCCCCCCCCCCCCCCN(O)CCCCCCCCCCCCCCCCCC ITUWQZXQRZLLCR-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- KWUZCAVKPCRJPO-UHFFFAOYSA-N n-ethyl-4-(6-methyl-1,3-benzothiazol-2-yl)aniline Chemical compound C1=CC(NCC)=CC=C1C1=NC2=CC=C(C)C=C2S1 KWUZCAVKPCRJPO-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical class OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- VCAFTIGPOYBOIC-UHFFFAOYSA-N phenyl dihydrogen phosphite Chemical class OP(O)OC1=CC=CC=C1 VCAFTIGPOYBOIC-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
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- C08K5/13—Phenols; Phenolates
- C08K5/134—Phenols containing ester groups
- C08K5/1345—Carboxylic esters of phenolcarboxylic acids
-
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
- C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
- C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
- C08F236/14—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated containing elements other than carbon and hydrogen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/32—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing two or more of boron, silicon, phosphorus, selenium, tellurium or a metal
- C09K15/322—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing two or more of boron, silicon, phosphorus, selenium, tellurium or a metal containing only phosphorus
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
-
- 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
-
- 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
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
-
- 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
- C08K5/13—Phenols; Phenolates
-
- 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
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1535—Five-membered rings
-
- 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
- C08K5/17—Amines; Quaternary ammonium 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
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/22—Compounds containing nitrogen bound to another nitrogen atom
- C08K5/24—Derivatives of hydrazine
- C08K5/25—Carboxylic acid hydrazides
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/372—Sulfides, e.g. R-(S)x-R'
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
- C08K5/378—Thiols containing heterocyclic rings
-
- 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/38—Thiocarbonic acids; Derivatives thereof, e.g. xanthates ; i.e. compounds containing -X-C(=X)- groups, X being oxygen or sulfur, at least one X being sulfur
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
- C08K5/523—Esters of phosphoric acids, e.g. of H3PO4 with hydroxyaryl 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
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
- C08K5/526—Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl 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
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/527—Cyclic 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2
- C08K5/5333—Esters of phosphonic acids
- C08K5/5357—Esters of phosphonic acids cyclic
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5393—Phosphonous compounds, e.g. R—P(OR')2
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; 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
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
一种经改质的聚合物材料,包含一选自于烯烃系聚合物及乙烯/醋酸乙烯酯共聚物中至少一者的聚合物基材,以及一复合式安定剂组成物。复合式安定剂组成物包括一含有受阻酚类抗氧化剂及含磷有机抗氧化剂的抗氧化剂组分,以及一选自于化学式1至化学式4中至少一者的含硫羧酸盐。通过使用复合式安定剂组成物,使得经改质的聚合物材料在加工成型制程中具有良好的颜色稳定性及加工稳定性。【特征化学式】【化学式1】【化学式2】【化学式3】【化学式4】
Description
技术领域
本发明是涉及一种经改质的聚合物材料,特别是涉及一种通过一包括受阻酚类抗氧化剂、含磷有机抗氧化剂及特定的含硫羧酸盐化合物的复合式安定剂组成物将烯烃系聚合物或乙烯/醋酸乙烯酯共聚物改质的经改质的聚合物材料。
背景技术
聚合物基材,例如烯烃系聚合物、乙烯/醋酸乙烯酯共聚物具有良好的化学稳定性、机械强度、电气绝缘性及制品尺寸安定性,并具有无毒性且易于加工等优点,因而被广泛应用作为各种产品。聚合物基材虽具有上述优点,但上述聚合物基材在热能作用下容易被氧化降解,造成黄变以及机械性质下降。
因此,为了防止上述聚合物基材的氧化降解,可在加工成型制程中加入抗氧化剂来降低聚合物基材的氧化降解作用,以增强聚合物基材的机械性质及耐热性;然而,抗氧化剂本身可能导致聚合物基材带色及加工稳定性下降。此外,一般在加工成型制程中会再加入制酸剂,是为了抑制酸性物质造成聚合物基材降解,然而,某些制酸剂的种类或者添加量较多时,也会导致聚合物基材带色及加工稳定性下降。
发明内容
本发明的第一目的在于提供一种经改质的聚合物材料,其在加工成型制程中,能够维持良好的颜色稳定性及加工稳定性。
本发明经改质的聚合物材料包含:
一聚合物基材,是选自于烯烃系聚合物及乙烯/醋酸乙烯酯共聚物中至少一者;及
一复合式安定剂组成物,包括:
一具有受阻酚类抗氧化剂及含磷有机抗氧化剂的抗氧化剂组分,及
一选自于化学式1至化学式4中至少一者所示的含硫羧酸盐,
【化学式1】
【化学式2】
【化学式3】
【化学式4】
在化学式1中,Mq+表示Ca2+、Ba2+、Mg2+、Zn2+或Al3+,q表示2或3,t表示0至6的整数,R91表示氢或C1至C18烷基,R92表示C1至C30烷基、C6至C18芳烃基或R93表示C1至C30烷基或C6至C18芳烃基,k表示1至5的整数,
化学式2中,X11及X12各自独立地表示Ca2+、Ba2+、Mg2+或Zn2+,Y11及Y12各自独立地表示C1至C30烷基或C6至C18芳烃基,a及b各自独立地表示1至6的整数,
化学式3中,p表示1至9的整数,X21表示Ca2+、Ba2+、Mg2+或Zn2+,G1及G2各自独立地表示c及d各自独立地表示1至6的整数,且当p≥2时,多个G1可为相同或不同,多个X21可为相同或不同,
在化学式4中,X31表示Ca2+、Ba2+、Mg2+、Zn2+,Y31表示C1至C30烷基、C6至C18芳烃基或R93表示C1至C30烷基或C6至C18芳烃基,k表示1至5的整数。
本发明经改质的聚合物材料,所述复合式安定剂组成物还包括制酸剂及金属钝化剂中至少一者。
本发明经改质的聚合物材料,所述制酸剂是选自于脂肪酸盐。
本发明经改质的聚合物材料,所述金属钝化剂是选自于1,2-二[-(3,5-二-第三丁基-4-羟基苯基)丙酰基]肼及2,2'-草酰胺基[乙基3-(3,5-二-第三丁基-4-羟基苯基)丙酸酯]中至少一者。
本发明经改质的聚合物材料,所述抗氧化剂组分还具有苯并呋喃酮类抗氧化剂及氧化胺类抗氧化剂中至少一者。
本发明经改质的聚合物材料,以所述聚合物基材的重量为100重量份,所述复合式安定剂组成物的含量范围为0.01至5.0重量份。
本发明的第二目的在于提供一种复合式安定剂组成物,是用于改质上述的聚合物基材。
本发明复合式安定剂组成物包含:一包括受阻酚类抗氧化剂及含磷有机抗氧化剂的抗氧化剂组分,以及一选自于化学式1至化学式4中至少一者所示的含硫羧酸盐。其中,所述化学式1至4是如上所述,故不再赘述。
本发明复合式安定剂组成物,所述化学式1中的R91表示氢,R92表示C1至C18烷基、C6至C18芳烃基或R93表示C1至C18烷基,k表示1或2。
本发明复合式安定剂组成物,还包括制酸剂及金属钝化剂中至少一者。
本发明复合式安定剂组成物,所述抗氧化剂组分还包括苯并呋喃酮类抗氧化剂及氧化胺类抗氧化剂中至少一者。
本发明的有益效果在于:通过在所述聚合物基材中添加含有受阻酚类抗氧化剂、含磷有机抗氧化剂及特定的含硫羧酸盐的所述复合式安定剂组成物,使得所述经改质的聚合物材料在加工制程中能维持良好的颜色稳定性及加工稳定性,继而制得高质量的成型品。
具体实施方式
以下将就本发明内容进行详细说明:
[聚合物基材]
所述聚合物基材是选自于烯烃系聚合物及乙烯/醋酸乙烯酯共聚物中的至少一者。较佳地,所述烯烃系聚合物是选自于聚乙烯、聚丙烯中至少一者。
[复合式安定剂组成物]
[抗氧化剂组分]
所述抗氧化剂组分具有受阻酚类抗氧化剂及含磷有机抗氧化剂。较佳地,所述抗氧化剂组分还具有苯并呋喃酮类抗氧化剂及氧化胺类抗氧化剂中至少一者。
所述受阻酚类抗氧化剂例如但不限于:四[β-(3,5-二叔丁基-4-羟基苯基)丙酸]季戊四醇酯(以下简称抗氧化剂1010)、二缩三乙二醇双[β-(3-叔丁基-4-羟基-5-甲基苯基)丙酸酯](简称抗氧化剂245)、1,3,5-三甲基-2,4,6-三(3,5-二叔丁基-4-羟基苄基)苯(以下简称抗氧化剂1330)、1,3,5-三(3,5-二叔丁基-4-羟基苄基)异氰尿酸酯(简称抗氧化剂3114)、三(丁基甲酚基)丁烷(简称AO-30)、4,4'-亚丁基双(6-叔丁基-3-甲基苯酚)(简称AO-40)、N,N'-双[3-(3,5-二叔丁基-4-羟基苯基)丙酰]肼(简称抗氧化剂1024)、N,N'-双-[3-(3,5-二叔丁基-4-羟基苯基)丙酰基]己二胺(简称抗氧化剂1098)、2,2'-亚甲基双-(4-甲基-6-叔丁基苯酚)(简称抗氧化剂2246),以及3,5-二叔丁基-4-羟基苯丙酸异辛酯(简称抗氧化剂1135)等,上述受阻酚类抗氧化剂可单独一种或混合多种使用。
所述含磷有机抗氧化剂例如但不限于:3,9-双(2,4-二异丙苯基苯氧基)-2,4,8,10-四氧杂-3,9-二磷杂螺[5.5]十一烷(简称抗氧化剂9228)、三(2,4-二叔丁基)亚磷酸苯酯(以下简称抗氧化剂168)、二硬脂基季戊四醇二亚磷酸酯(简称抗氧化剂618)、双(2,4-二叔丁基苯基)季戊四醇二亚磷酸酯(以下简称抗氧化剂626)、2,4,8,10-四第三丁基-6-[(2-乙己基)氧]-12H-二苯基[d,g][1,3,2]二氧磷杂八环(简称HP-10)、9,10-二氢-9-氧杂-10-磷杂菲-10-氧化物(简称DOPO)等,上述含磷有机抗氧化剂可以单独一种或混合多种使用。
所述苯并呋喃酮类抗氧化剂例如但不限于:二甲苯基二丁基苯并呋喃酮(xylyldibutylbenzofuranone,简称抗氧化剂HP-136)、5-(叔丁基)-3-[5-(叔丁基)-2-羟基苯基]苯并呋喃-2-(3H)-酮{5-(tert-Butyl)-3-[5-(tert-butyl)-2-hydroxyphenyl]benzofuran-2(3H)-one,CAS号码为214354-68-4}、3-[3,5-双(1,1-二甲基乙基)-2-羟基苯基]-5,7-双(1,1-二甲基乙基)-2(3H)-苯并呋喃酮{3-[3,5-bis(1,1-dimethylethyl)-2-hydroxyphenyl]-5,7-bis(1,1-dimethylethyl)-2(3H)-benzofuranone,CAS号码为210709-72-1}等,上述苯并呋喃酮类抗氧化剂可以单独一种或混合多种使用。
所述氧化胺类抗氧化剂例如但不限于:双(烷基氢化脂肪)氧化胺、双(十八烷基)羟胺(简称抗氧化剂FS042)等,上述氧化胺类抗氧化剂可以单独一种或混合多种使用。
以所述聚合物基材的总量为100重量份,所述受阻酚类抗氧化剂的含量范围为0.01至2.5重量份,及所述含磷有机抗氧化剂的含量范围为0.01至4.5重量份。
以所述聚合物基材的总量为100重量份,苯并呋喃酮类抗氧化剂的含量范围为0至0.5重量份;氧化胺类抗氧化剂的含量范围为0至1.0重量份。
[含硫羧酸盐]
所述含硫羧酸盐是选自于化学式1至化学式4中至少一者。
较佳地,所述化学式1中的R91表示氢,R92表示C1至C18烷基、C6至C18芳烃基或其中,R93表示C1至C18烷基,k表示1或2。上述的芳烃基指的是芳基、烃基取代的芳基或芳基取代的烃基。更佳地,所述化学式1中的R92表示十二烷基或所述化学式1所示的含硫羧酸盐例如但不限于:2-十二烷基硫基乙酸锌、2-十二烷基硫基乙酸钙、3-十二烷基硫基丙酸锌、3-十二烷基硫基丙酸钙或3-十八烷基硫基丙酸铝。
较佳地,所述化学式2中,X11及X12各自独立地表示Ca或Zn,Y11及Y12各自独立地表示-C7H15或-C17H35。所述化学式2所示的含硫羧酸盐例如但不限于:
较佳地,所述化学式3中,X21表示Ca或Zn,G1及G2各自独立地表示其中c及d各自独立地表示1或2。所述化学式3所示的含硫羧酸盐例如但不限于:
其中,p表示1至9的整数。
所述化学式4所示的含硫羧酸盐例如但不限于:
以所述聚合物基材的总量为100重量份,所述含硫羧酸盐的含量范围为0.01至1.5重量份。
[制酸剂及金属钝化剂]
较佳地,所述复合式安定剂组成物还包括制酸剂及金属钝化剂中的至少一者。
所述制酸剂与所述抗氧化剂组分并用,能够更有助于平衡所述经改质的聚合物材料的酸碱值,并使所述抗氧化剂组分与所述含硫羧酸盐更易相容。更佳地,所述制酸剂是选自于脂肪酸盐。所述脂肪酸盐例如但不限于:硬脂酸钙、硬脂酸锌、二十二酸镁、硬脂酸镁、蓖麻油酸钠(sodium ricinoleate)、棕榈酸钾(potassium palmitate),上述脂肪酸盐可单独一种或混合多种使用。
所述金属钝化剂能够进一步防止所述经改质的聚合物材料的性质劣化。更佳地,所述金属钝化剂是选自于1,2-二[-(3,5-二-叔丁基-4-羟基苯基)丙酰基]肼{1,2-di[-(3,5-di-tert-butyl-4-hydroxyphenyl)propionyl]hydrazide}及2,2'-草酰胺基[乙基3-(3,5-二-叔丁基-4-羟基苯基)丙酸酯]{2,2'-oxamidobis[ethyl3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate]}中的至少一者。所述金属钝化剂的具体商品例如但不限于:MD-1024、Naugard XL-1、Eastman Inhibitor OABH。
以所述聚合物基材的总量为100重量份,制酸剂的含量范围为0至1.5重量份;所述金属钝化剂的含量范围为0至1.0重量份。
[经改质的聚合物材料]
较佳地,以所述聚合物基材的重量为100重量份,所述复合式安定剂组成物的含量范围为0.01至5.0重量份。
所述经改质的聚合物材料的制备方法并无特别限制,例如但不限于将所述聚合物基材与所述复合式安定剂组成物混合即可。
所述经改质的聚合物材料的加工成型方式并无特别限制,可依据后续的产品需求,采用烯烃系聚合物、乙烯/醋酸乙烯酯共聚物常用的加工成型方式即可。所述加工成型的方式例如但不限于押出成型、射出成型等。
【实施方式】
本发明将就以下实施例来作进一步说明,但应了解的是,所述实施例仅为例示说明,而不应被解释为本发明实施的限制。
[实验药品]
1.聚丙烯:购自于台化公司,品名为B8001,表1及表2中简称PP。
2.聚乙烯:购自于台塑公司,品名为LL120,表1及表2中简称PE。
3.四[β-(3,5-二叔丁基-4-羟基苯基)丙酸]季戊四醇酯:为受阻酚类抗氧化剂,表1及表2中简称A1。
4.1,3,5-三甲基-2,4,6-三(3,5-二叔丁基-4-羟基苄基)苯:为受阻酚类抗氧化剂,表1及表2中简称A2。
5.三(2,4-二叔丁基)亚磷酸苯酯:为含磷有机抗氧化剂,表1及表2中简称A3。
6.双(2,4-二叔丁基苯基)季戊四醇二亚磷酸酯:为含磷有机抗氧化剂,表1及表2中简称A4。
7.二甲苯基二丁基苯并呋喃酮:为苯并呋喃酮类抗氧化剂,表1及表2中简称A5。
8.双(十八烷基)羟胺:为氧化胺类抗氧化剂,表1及表2中简称A6。
9.[C12H25─S─CH2CH2COO]2Ca:为化学式1所示的含硫羧酸盐,表1及表2中简称B1。
10.[C12H25─S─CH2CH2COO]3Al:为化学式1所示的含硫羧酸盐,表1及表2中简称B2。
11.[H17C8OOCCH2─S─CH2CH2COO]2Ca:为化学式1所示的含硫羧酸盐,表1及表2中简称B3。
12.为化学式4所示的含硫羧酸盐,表1及表2中简称B4。
13.为化学式2所示的含硫羧酸盐,表1及表2中简称B5;
14.为化学式3所示的含硫羧酸盐,表1及表2中简称B6。
15.硬脂酸钙:为制酸剂。
16.1,2-二[-(3,5-二-叔丁基-4-羟基苯基)丙酰基]肼:为金属钝化剂,表1及表2中简称MD-1024。
17.硫代二丙酸双十八酯:英文名为disteaxyl thiodipropionate,以下简称DSTDP。
<实施例1至27>经改质的聚合物材料
依据表1所示的组成成分及比例(重量份),将100重量份聚丙烯或100重量份聚乙烯分别与复合式安定剂组成物在25℃下均匀混合,分别得到实施例1至27的经改质的聚合物材料E1'至E27'。
<比较例1至10>经改质的聚合物材料
依据表2所示的组成成分及比例(重量份),将100重量份聚丙烯或100重量份聚乙烯分别与安定剂组成物在25℃下均匀混合,分别得到比较例1至10的经改质的聚合物材料CE1'至CE10'。
[评价测试]
将上述经改质的聚合物材料E1'至E27'以及CE1'至CE10'分别以双螺杆押出机(台湾弘煜机械公司试验机PSM20A)混合押出(温度设置为190至230℃,螺杆转速为200转/分钟,进料速度为6转/分钟),再经过冷却、风干、切粒、干燥,制备出样品E1至E27及CE1至CE10。将样品E1至E27及CE1至CE10分别重复进行上述押出、冷却、风干、切粒、干燥步骤,以评估样品在经过多次加工成型的程序后黄色度及熔融指数的变化,黄色度的变化越小代表经改质的聚合物材料在加工成型制程中的颜色稳定性越佳,熔融指数的变化越小代表经改质的聚合物材料在加工成型制程中的加工稳定性越佳。
1.黄色色差(Δb*值)
使用色差仪(为HunterLab公司的ColorQuest XE)分别测量样品E1至E27及CE1至CE10在第3次及第5次押出后相较于第1次押出的黄色色差(Δb*值)。
2.熔融指数变化(ΔMI)
使用实验室熔融指数仪(为Dynisco公司的Laboratory Melt Indexer LMID4004)分别测量样品E1至E27及CE1至CE10在第3次及第5次押出后相较于第1次押出的熔融指数变化
黄色色差(Δb*值)及熔融指数变化(ΔMI)的评价测试结果如表3及表4中所示,表3是聚合物基材为聚乙烯的实施例及比较例,表4是聚合物基材为聚丙烯的实施例及比较例。
表1
表2
注:表1及表2中,「-」表示无添加。
表3
表4
由表3及表4得知,就聚合物基材为聚乙烯的经改质的聚合物材料来看,由实施例22至27制得的样品E22至E27,经第3次押出的Δb*值在2.23至2.69,经第5次押出的Δb*值在3.97至4.71,然而,由比较例10制得的样品CE10,经第3次押出的Δb*值为3.06,经第5次押出的Δb*值为在5.45。就聚合物基材为聚丙烯的经改质的聚合物材料来看,由实施例1至21制得的样品E1至E21,经第3次押出的Δb*值在2.29至2.97,经第5次押出的Δb*值在4.12至5.36,然而,由比较例1至9制得的样品CE 1至CE9,经第3次押出的Δb*值在3.51以上,经第5次押出的Δb*值在6.27以上。显示不论聚合物基材为聚乙烯或聚丙烯,相较于比较例1至10使用安定剂组成物,实施例1至27经改质的聚合物材料通过使用所述复合式安定剂组成物,使得经改质的聚合物材料具有较佳的颜色稳定性,进而使得所制得的样品具有较低的黄色色差(Δb*值),黄变较不明显。
根据熔融指数变化(ΔMI)的结果,就聚合物基材为聚乙烯的经改质的聚合物材料来看,由实施例22至27制得的样品E22至E27,经第3次押出的ΔMI在113.58%至126.78%,经第5次押出的ΔMI在178.40%至192.55%;然,由比较例10制得的样品CE10,经第3次押出的ΔMI在153.42%,经第5次押出的ΔMI在263.65%。就聚合物基材为聚丙烯的经改质的聚合物材料来看,由实施例1至21制得的样品E1至E21,经第3次押出的ΔMI在103.33%至160.92%,经第5次押出的ΔMI在185.56%至265.46%,然而,由比较例1至9制得的样品CE1至CE9,经第3次押出的ΔMI值在188.76%以上,经第5次押出的ΔMI值在362.62%以上。显示不论聚合物基材为聚乙烯或聚丙烯,相较于比较例1至10使用安定剂组成物,实施例1至27经改质的聚合物材料通过使用所述复合式安定剂组成物,使得经改质的聚合物材料具有较佳的加工稳定性(物性),进而使得所制得的样品具有较低的熔融指数变化(ΔMI)。
综上所述,本发明通过在所述聚合物基材中添加含有受阻酚类抗氧化剂、含磷有机抗氧化剂及特定的含硫羧酸盐的所述复合式安定剂组成物,使得所述经改质的聚合物材料在加工制程中能维持良好的颜色稳定性及加工稳定性,故确实能达成本发明的目的。
Claims (10)
1.一种经改质的聚合物材料,其特征在于其包含:
一聚合物基材,是选自于烯烃系聚合物及乙烯/醋酸乙烯酯共聚物中至少一者;及
一复合式安定剂组成物,包括:
一具有受阻酚类抗氧化剂及含磷有机抗氧化剂的抗氧化剂组分,及
一选自于化学式1、化学式2及化学式4中至少一者的含硫羧酸盐,
【化学式1】
【化学式2】
【化学式4】
在化学式1中,Mq+表示Ca2+、Ba2+、Mg2+、Zn2+或Al3+,q表示2或3,t表示0至6的整数,R91表示氢或C1至C18烷基,R92表示C1至C30烷基、C6至C18芳烃基或R93表示C1至C30烷基或C6至C18芳烃基,k表示1至5的整数,
化学式2中,X11及X12各自独立地表示Ca2+、Ba2+、Mg2+或Zn2+,Y11及Y12各自独立地表示C1至C30烷基或C6至C18芳烃基,a及b各自独立地表示1至6的整数,
在化学式4中,X31表示Ca2+、Ba2+、Mg2+、Zn2+,Y31表示C1至C30烷基、C6至C18芳烃基或R93表示C1至C30烷基或C6至C18芳烃基,k表示1至5的整数。
2.根据权利要求1所述的经改质的聚合物材料,其特征在于,所述复合式安定剂组成物还包括制酸剂及金属钝化剂中至少一者。
3.根据权利要求2所述的经改质的聚合物材料,其特征在于,
所述制酸剂是选自于脂肪酸盐。
4.根据权利要求2所述的经改质的聚合物材料,其特征在于,所述金属钝化剂是选自于1,2-二[-(3,5-二-第三丁基-4-羟基苯基)丙酰基]肼及2,2'-草酰胺基[乙基3-(3,5-二-第三丁基-4-羟基苯基)丙酸酯]中至少一者。
5.根据权利要求1所述的经改质的聚合物材料,其特征在于,所述抗氧化剂组分还具有苯并呋喃酮类抗氧化剂及氧化胺类抗氧化剂中至少一者。
6.根据权利要求1所述的经改质的聚合物材料,其特征在于,以所述聚合物基材的重量为100重量份,所述复合式安定剂组成物的含量范围为0.01至5.0重量份。
7.一种复合式安定剂组成物,其特征在于其包含:
一包括受阻酚类抗氧化剂及含磷有机抗氧化剂的抗氧化剂组分;及
一选自于化学式1、化学式2及化学式4中至少一者的含硫羧酸盐;
【化学式1】
【化学式2】
【化学式4】
在化学式1中,Mq+表示Ca2+、Ba2+、Mg2+、Zn2+或Al3+,q表示2或3,t表示0至6的整数,R91表示氢或C1至C18烷基,R92表示C1至C30烷基、C6至C18芳烃基或R93表示C1至C30烷基或C6至C18芳烃基,k表示1至5的整数;
化学式2中,X11及X12各自独立地表示Ca2+、Ba2+、Mg2+或Zn2+,Y11及Y12各自独立地表示C1至C30烷基或C6至C18芳烃基,a及b各自独立地表示1至6的整数;
在化学式4中,X31表示Ca2+、Ba2+、Mg2+、Zn2+,Y31表示C1至C30烷基、C6至C18芳烃基或R93表示C1至C30烷基或C6至C18芳烃基,k表示1至5的整数。
8.根据权利要求7所述的复合式安定剂组成物,其特征在于,所述化学式1中的R91表示氢,R92表示C1至C18烷基、C6至C18芳烃基或R93表示C1至C18烷基,k表示1或2。
9.根据权利要求7所述的复合式安定剂组成物,其特征在于其还包括制酸剂及金属钝化剂中至少一者。
10.根据权利要求7所述的复合式安定剂组成物,其特征在于,所述抗氧化剂组分还包括苯并呋喃酮类抗氧化剂及氧化胺类抗氧化剂中至少一者。
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
TW104128114 | 2015-08-27 | ||
TW104128114 | 2015-08-27 | ||
TW105103696 | 2016-02-04 | ||
TW105103696 | 2016-02-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106479041A CN106479041A (zh) | 2017-03-08 |
CN106479041B true CN106479041B (zh) | 2019-04-26 |
Family
ID=58273845
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610674076.1A Pending CN106479015A (zh) | 2015-08-27 | 2016-08-16 | 经改质的聚合物材料及复合式安定剂组成物 |
CN201610674278.6A Active CN106479041B (zh) | 2015-08-27 | 2016-08-16 | 经改质的聚合物材料及复合式安定剂组成物 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610674076.1A Pending CN106479015A (zh) | 2015-08-27 | 2016-08-16 | 经改质的聚合物材料及复合式安定剂组成物 |
Country Status (6)
Country | Link |
---|---|
KR (1) | KR102003595B1 (zh) |
CN (2) | CN106479015A (zh) |
BR (1) | BR102017017764A2 (zh) |
ES (1) | ES2836703T3 (zh) |
RU (1) | RU2678593C1 (zh) |
TW (2) | TWI599604B (zh) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN109294151B (zh) * | 2017-07-24 | 2021-03-09 | 奕益实业股份有限公司 | 经改性的聚合物材料及用于制备聚合物材料的混合物 |
TWI647273B (zh) * | 2017-07-24 | 2019-01-11 | 奕益實業有限公司 | Modified polymeric material and mixture for preparing polymeric materials |
CN109880347A (zh) * | 2019-03-07 | 2019-06-14 | 禾聚实业有限公司 | 聚胺酯材料 |
CN115368630B (zh) * | 2021-05-17 | 2024-04-09 | 天津利安隆新材料股份有限公司 | 用于生橡胶的液体抗氧化剂组合物及其应用 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1220602B (de) * | 1960-08-04 | 1966-07-07 | Bergwerksgesellschaft Hibernia | Verfahren zum Stabilisieren von Polyolefinen |
CN101003643A (zh) * | 2006-12-30 | 2007-07-25 | 中国科学院广州化学研究所 | 一种含卤素聚合物用的含硫有机羧酸金属盐复合稳定剂及其应用 |
CN102432961A (zh) * | 2011-11-16 | 2012-05-02 | 山东瑞丰高分子材料股份有限公司 | 一种pvc用复合热稳定剂及其制备方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL265210A (zh) * | 1960-05-27 | |||
SU593451A1 (ru) * | 1976-04-21 | 1999-12-27 | В.Н. Забористов | Способ стабилизации бутилкаучука |
KR19990044338A (ko) * | 1995-08-29 | 1999-06-25 | 만셀 케이쓰 로드니 | 내방사선성 폴리프로필렌 및 그로부터 제조된 제품 |
JPH10101687A (ja) * | 1996-08-07 | 1998-04-21 | Sumitomo Chem Co Ltd | 亜リン酸エステル類、その製造方法及びその用途 |
JP3951367B2 (ja) * | 1996-11-28 | 2007-08-01 | 住友化学株式会社 | 5価のリン系化合物を有効成分とする熱可塑性樹脂用安定剤、その製造方法およびその用途 |
DE60331613D1 (de) * | 2003-03-28 | 2010-04-15 | Mitsui Chemicals Inc | Propylen-Copolymer, Polypropylen-Zusammensetzung, Verwendung davon, Übergangsmetallverbindungen und Katalysatoren zur Olefin-Polymerisation |
KR101412264B1 (ko) * | 2006-11-24 | 2014-06-25 | 미츠비시 레이온 가부시키가이샤 | 폴리올레핀계 수지용 안정화제 및 안정화된 폴리올레핀계 수지 조성물 |
-
2016
- 2016-08-16 CN CN201610674076.1A patent/CN106479015A/zh active Pending
- 2016-08-16 CN CN201610674278.6A patent/CN106479041B/zh active Active
- 2016-08-19 TW TW105126497A patent/TWI599604B/zh active
- 2016-08-19 TW TW105126496A patent/TWI650359B/zh active
-
2017
- 2017-08-14 ES ES17186089T patent/ES2836703T3/es active Active
- 2017-08-14 RU RU2017128892A patent/RU2678593C1/ru active
- 2017-08-16 KR KR1020170103454A patent/KR102003595B1/ko active IP Right Grant
- 2017-08-18 BR BR102017017764-5A patent/BR102017017764A2/pt not_active Application Discontinuation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1220602B (de) * | 1960-08-04 | 1966-07-07 | Bergwerksgesellschaft Hibernia | Verfahren zum Stabilisieren von Polyolefinen |
CN101003643A (zh) * | 2006-12-30 | 2007-07-25 | 中国科学院广州化学研究所 | 一种含卤素聚合物用的含硫有机羧酸金属盐复合稳定剂及其应用 |
CN102432961A (zh) * | 2011-11-16 | 2012-05-02 | 山东瑞丰高分子材料股份有限公司 | 一种pvc用复合热稳定剂及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
TWI650359B (zh) | 2019-02-11 |
TWI599604B (zh) | 2017-09-21 |
CN106479015A (zh) | 2017-03-08 |
ES2836703T3 (es) | 2021-06-28 |
TW201708357A (zh) | 2017-03-01 |
BR102017017764A2 (pt) | 2019-04-16 |
CN106479041A (zh) | 2017-03-08 |
KR102003595B1 (ko) | 2019-07-24 |
RU2678593C1 (ru) | 2019-01-30 |
TW201708347A (zh) | 2017-03-01 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106479041B (zh) | 经改质的聚合物材料及复合式安定剂组成物 | |
CN102791788B (zh) | 具有环氧化脂肪酸酯增塑剂的热稳定聚合物组合物 | |
CN102675269B (zh) | 苯并呋喃衍生物及其应用 | |
CN108047493B (zh) | 一种用于尼龙的抗氧化剂组合物 | |
WO2017121223A1 (zh) | 一种pbat树脂组合物 | |
CN110423397A (zh) | 一种抗氧化稳定剂组合物及其在聚乙烯膜料中的应用 | |
CN109963902A (zh) | 耗散因子和添加剂接受性平衡的组合物 | |
CN107254085A (zh) | 一种具有高抗氧化性能的聚烯烃助剂组合物 | |
CN110256844A (zh) | 一种3d打印用耐黄变尼龙复合材料及其制备方法 | |
CN110305366A (zh) | 一种抗氧化稳定剂组合物及改性顺丁橡胶 | |
CN109689758A (zh) | 可湿固化聚烯烃组合物 | |
CN106478983A (zh) | 复合式安定剂组成物及经改质的聚合物材料 | |
JP7082988B2 (ja) | ポリエチレン混合組成物 | |
CN107778525B (zh) | 一种聚乙烯电线电缆专用料的稳定剂组合物 | |
CN104583292B (zh) | 增塑剂和增塑的聚合物组合物 | |
TWI647273B (zh) | Modified polymeric material and mixture for preparing polymeric materials | |
CN104559091B (zh) | 一种高耐热、高韧性免底涂产品及其制备方法 | |
JP6676591B2 (ja) | 変性ポリマー組成物及びそれを製造するための安定剤混合物 | |
CN107955207B (zh) | 橡胶防老剂组合物及其制备方法和应用 | |
CN109294151B (zh) | 经改性的聚合物材料及用于制备聚合物材料的混合物 | |
TWI696610B (zh) | 複合型抗氧化劑、塑料組合物及其塑料產品 | |
TW201708336A (zh) | 複合式安定劑組成物及經改質的聚合物材料 | |
EP3284779B1 (en) | Modified polymer composition and stabilizer mixture for making the same | |
RU2256676C2 (ru) | Композиция на основе синтетического каучука для заполнения кабелей | |
CN106336624A (zh) | Pet母粒及其制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
CB02 | Change of applicant information | ||
CB02 | Change of applicant information |
Address after: Taipei City, Taiwan, China Applicant after: FDC Lees Chemical Industry Co., Ltd. Address before: Taipei City, Taiwan, China Applicant before: FDC Lees Chemical Industry Co., Ltd. |
|
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CP03 | Change of name, title or address | ||
CP03 | Change of name, title or address |
Address after: 18 / F, 102 Roosevelt Road, Zhongzheng District, Taipei, Taiwan, China Patentee after: Yiyi Industry Co.,Ltd. Address before: Taipei City, Taiwan, China Patentee before: FDC,LEES CHEMICAL INDUSTRY Co.,Ltd. |