CN1239591C - 稳定剂组合物和稳定热塑性聚合物的方法 - Google Patents
稳定剂组合物和稳定热塑性聚合物的方法 Download PDFInfo
- Publication number
- CN1239591C CN1239591C CNB028155130A CN02815513A CN1239591C CN 1239591 C CN1239591 C CN 1239591C CN B028155130 A CNB028155130 A CN B028155130A CN 02815513 A CN02815513 A CN 02815513A CN 1239591 C CN1239591 C CN 1239591C
- Authority
- CN
- China
- Prior art keywords
- alkyl
- heteroatomic
- cycloalkyl
- hydrogen
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 229920000098 polyolefin Polymers 0.000 title abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 83
- 239000003381 stabilizer Substances 0.000 claims abstract description 24
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 6
- -1 amine compound Chemical class 0.000 claims description 118
- 229910052760 oxygen Inorganic materials 0.000 claims description 91
- 229910052698 phosphorus Inorganic materials 0.000 claims description 70
- 239000001257 hydrogen Substances 0.000 claims description 38
- 229910052739 hydrogen Inorganic materials 0.000 claims description 38
- 229910052717 sulfur Inorganic materials 0.000 claims description 36
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 35
- 150000001875 compounds Chemical class 0.000 claims description 30
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 claims description 23
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 19
- 239000000126 substance Substances 0.000 claims description 15
- 229920000642 polymer Polymers 0.000 claims description 14
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 12
- 150000002431 hydrogen Chemical group 0.000 claims description 8
- 239000011574 phosphorus Substances 0.000 claims description 8
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 150000003053 piperidines Chemical class 0.000 claims description 7
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 125000001072 heteroaryl group Chemical group 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 claims description 4
- DMCLNIZKWQGPTM-UHFFFAOYSA-N 5-bromo-2-[(3-octoxyphenyl)methylsulfanyl]benzoic acid Chemical compound CCCCCCCCOC1=CC=CC(CSC=2C(=CC(Br)=CC=2)C(O)=O)=C1 DMCLNIZKWQGPTM-UHFFFAOYSA-N 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 230000003019 stabilising effect Effects 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract description 51
- 239000000835 fiber Substances 0.000 abstract description 9
- 238000012545 processing Methods 0.000 abstract description 9
- 238000009472 formulation Methods 0.000 abstract description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 abstract description 4
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 239000007789 gas Substances 0.000 abstract description 3
- 238000002845 discoloration Methods 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 description 64
- 150000002148 esters Chemical class 0.000 description 47
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 39
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 25
- 150000001412 amines Chemical class 0.000 description 25
- 229920001577 copolymer Polymers 0.000 description 24
- 239000004743 Polypropylene Substances 0.000 description 22
- 229920001155 polypropylene Polymers 0.000 description 22
- 239000001301 oxygen Substances 0.000 description 21
- 239000002585 base Substances 0.000 description 19
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 19
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Natural products OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 17
- 239000002253 acid Substances 0.000 description 16
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 13
- 150000001408 amides Chemical class 0.000 description 13
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 12
- 239000012964 benzotriazole Substances 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 10
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 10
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 10
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 10
- 239000005864 Sulphur Substances 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 10
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 10
- 238000005804 alkylation reaction Methods 0.000 description 9
- 239000003963 antioxidant agent Substances 0.000 description 9
- 230000003078 antioxidant effect Effects 0.000 description 9
- 235000006708 antioxidants Nutrition 0.000 description 9
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 9
- 125000003003 spiro group Chemical group 0.000 description 9
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 8
- 239000000654 additive Substances 0.000 description 8
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 8
- KBPLFHHGFOOTCA-UHFFFAOYSA-N caprylic alcohol Natural products CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 8
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 8
- 150000002596 lactones Chemical class 0.000 description 8
- 239000011777 magnesium Substances 0.000 description 8
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 8
- 229940059574 pentaerithrityl Drugs 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 230000006641 stabilisation Effects 0.000 description 8
- 238000011105 stabilization Methods 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 7
- 239000008116 calcium stearate Substances 0.000 description 7
- 235000013539 calcium stearate Nutrition 0.000 description 7
- 239000007795 chemical reaction product Substances 0.000 description 7
- 239000007859 condensation product Substances 0.000 description 7
- 229920001903 high density polyethylene Polymers 0.000 description 7
- 239000004700 high-density polyethylene Substances 0.000 description 7
- 229920006324 polyoxymethylene Polymers 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical group C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 6
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 6
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 6
- 229920000573 polyethylene Polymers 0.000 description 6
- 239000004800 polyvinyl chloride Substances 0.000 description 6
- 229920000915 polyvinyl chloride Polymers 0.000 description 6
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 6
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical class CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 6
- AJPLOCYCAUFFFR-UHFFFAOYSA-N 11-thiophen-3-ylundecan-1-ol Chemical compound OCCCCCCCCCCCC=1C=CSC=1 AJPLOCYCAUFFFR-UHFFFAOYSA-N 0.000 description 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 5
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 5
- ICHKVCYUNCKCGL-UHFFFAOYSA-N CN(C)C.OCCCCCCO Chemical compound CN(C)C.OCCCCCCO ICHKVCYUNCKCGL-UHFFFAOYSA-N 0.000 description 5
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 5
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 5
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 5
- 239000004721 Polyphenylene oxide Substances 0.000 description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 5
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 5
- 230000000996 additive effect Effects 0.000 description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 5
- 150000001993 dienes Chemical class 0.000 description 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 5
- ZJIPHXXDPROMEF-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite Chemical compound OP(O)OP(O)O ZJIPHXXDPROMEF-UHFFFAOYSA-N 0.000 description 5
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 5
- 150000002429 hydrazines Chemical class 0.000 description 5
- 229910001701 hydrotalcite Inorganic materials 0.000 description 5
- 229960001545 hydrotalcite Drugs 0.000 description 5
- COVMBDWAODLWIB-UHFFFAOYSA-N n'-(2-hydroxyethyl)oxamide Chemical compound NC(=O)C(=O)NCCO COVMBDWAODLWIB-UHFFFAOYSA-N 0.000 description 5
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 5
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 5
- 229940038384 octadecane Drugs 0.000 description 5
- 239000004417 polycarbonate Substances 0.000 description 5
- 229920006380 polyphenylene oxide Polymers 0.000 description 5
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 5
- 239000002516 radical scavenger Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 5
- 229950006389 thiodiglycol Drugs 0.000 description 5
- 229960001124 trientine Drugs 0.000 description 5
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 5
- 229920002554 vinyl polymer Polymers 0.000 description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical group CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 4
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 4
- 229920002943 EPDM rubber Polymers 0.000 description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 4
- 229920002396 Polyurea Polymers 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- BEIOEBMXPVYLRY-UHFFFAOYSA-N [4-[4-bis(2,4-ditert-butylphenoxy)phosphanylphenyl]phenyl]-bis(2,4-ditert-butylphenoxy)phosphane Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(C=1C=CC(=CC=1)C=1C=CC(=CC=1)P(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)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 BEIOEBMXPVYLRY-UHFFFAOYSA-N 0.000 description 4
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 4
- HCPOCMMGKBZWSJ-UHFFFAOYSA-N ethyl 3-hydrazinyl-3-oxopropanoate Chemical compound CCOC(=O)CC(=O)NN HCPOCMMGKBZWSJ-UHFFFAOYSA-N 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 229920000092 linear low density polyethylene Polymers 0.000 description 4
- 239000004707 linear low-density polyethylene Substances 0.000 description 4
- 230000007774 longterm Effects 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- RZJRJXONCZWCBN-NJFSPNSNSA-N octadecane Chemical class CCCCCCCCCCCCCCCCC[14CH3] RZJRJXONCZWCBN-NJFSPNSNSA-N 0.000 description 4
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 235000019260 propionic acid Nutrition 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229960002920 sorbitol Drugs 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 3
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 3
- HTSVYUUXJSMGQC-UHFFFAOYSA-N 2-chloro-1,3,5-triazine Chemical class ClC1=NC=NC=N1 HTSVYUUXJSMGQC-UHFFFAOYSA-N 0.000 description 3
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 3
- SWZOQAGVRGQLDV-UHFFFAOYSA-N 4-[2-(4-hydroxy-2,2,6,6-tetramethylpiperidin-1-yl)ethoxy]-4-oxobutanoic acid Chemical compound CC1(C)CC(O)CC(C)(C)N1CCOC(=O)CCC(O)=O SWZOQAGVRGQLDV-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 239000004716 Ethylene/acrylic acid copolymer Substances 0.000 description 3
- YIKSCQDJHCMVMK-UHFFFAOYSA-N Oxamide Chemical compound NC(=O)C(N)=O YIKSCQDJHCMVMK-UHFFFAOYSA-N 0.000 description 3
- 229920002367 Polyisobutene Polymers 0.000 description 3
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 3
- 239000001273 butane Substances 0.000 description 3
- CCRCUPLGCSFEDV-UHFFFAOYSA-N cinnamic acid methyl ester Natural products COC(=O)C=CC1=CC=CC=C1 CCRCUPLGCSFEDV-UHFFFAOYSA-N 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 3
- 125000004494 ethyl ester group Chemical group 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 229920000554 ionomer Polymers 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- ODGYWRBCQWKSSH-UHFFFAOYSA-N n'-ethylpropane-1,3-diamine Chemical compound CCNCCCN ODGYWRBCQWKSSH-UHFFFAOYSA-N 0.000 description 3
- FTWUXYZHDFCGSV-UHFFFAOYSA-N n,n'-diphenyloxamide Chemical compound C=1C=CC=CC=1NC(=O)C(=O)NC1=CC=CC=C1 FTWUXYZHDFCGSV-UHFFFAOYSA-N 0.000 description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 3
- 125000002347 octyl 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])[H] 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N pentanoic acid group Chemical group C(CCCC)(=O)O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920001707 polybutylene terephthalate Polymers 0.000 description 3
- 229920000570 polyether Polymers 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 229920001897 terpolymer Polymers 0.000 description 3
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 3
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 239000004711 α-olefin Substances 0.000 description 3
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 3
- 150000000182 1,3,5-triazines Chemical class 0.000 description 2
- OTEKOJQFKOIXMU-UHFFFAOYSA-N 1,4-bis(trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=C(C(Cl)(Cl)Cl)C=C1 OTEKOJQFKOIXMU-UHFFFAOYSA-N 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
- FTVFPPFZRRKJIH-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CC1(C)CC(N)CC(C)(C)N1 FTVFPPFZRRKJIH-UHFFFAOYSA-N 0.000 description 2
- QIQBUIJPSSQASA-UHFFFAOYSA-N 2,6-dichloro-4-(2,4,4-trimethylpentan-2-yl)-2h-1,3,5-triazin-1-amine Chemical compound CC(C)(C)CC(C)(C)C1=NC(Cl)N(N)C(Cl)=N1 QIQBUIJPSSQASA-UHFFFAOYSA-N 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- IKEHOXWJQXIQAG-UHFFFAOYSA-N 2-tert-butyl-4-methylphenol Chemical class CC1=CC=C(O)C(C(C)(C)C)=C1 IKEHOXWJQXIQAG-UHFFFAOYSA-N 0.000 description 2
- BKZXZGWHTRCFPX-UHFFFAOYSA-N 2-tert-butyl-6-methylphenol Chemical class CC1=CC=CC(C(C)(C)C)=C1O BKZXZGWHTRCFPX-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 2
- CMBRHCVQODXRRS-UHFFFAOYSA-N 4-n-butan-2-ylbenzene-1,4-diamine Chemical class CCC(C)NC1=CC=C(N)C=C1 CMBRHCVQODXRRS-UHFFFAOYSA-N 0.000 description 2
- 235000021357 Behenic acid Nutrition 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- 239000004709 Chlorinated polyethylene Substances 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 2
- 229930040373 Paraformaldehyde Natural products 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 229930182556 Polyacetal Natural products 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 229920002877 acrylic styrene acrylonitrile Polymers 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000005250 alkyl acrylate group Chemical group 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229940116226 behenic acid Drugs 0.000 description 2
- QKLWAMMQKBOTCD-UHFFFAOYSA-N butane;diphenylphosphane Chemical compound CCCC.C=1C=CC=CC=1PC1=CC=CC=C1 QKLWAMMQKBOTCD-UHFFFAOYSA-N 0.000 description 2
- 210000004899 c-terminal region Anatomy 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 238000005660 chlorination reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 229960000452 diethylstilbestrol Drugs 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- FSRXIRGQJIHEFB-UHFFFAOYSA-N diphenylphosphane;ethane Chemical compound CC.C=1C=CC=CC=1PC1=CC=CC=C1 FSRXIRGQJIHEFB-UHFFFAOYSA-N 0.000 description 2
- SAMCXPGNUAXAOO-UHFFFAOYSA-N diphenylphosphane;pentane Chemical class CCCCC.C=1C=CC=CC=1PC1=CC=CC=C1 SAMCXPGNUAXAOO-UHFFFAOYSA-N 0.000 description 2
- ONDPGJBEBGWAKI-UHFFFAOYSA-N diphenylphosphane;propane Chemical compound CCC.C=1C=CC=CC=1PC1=CC=CC=C1 ONDPGJBEBGWAKI-UHFFFAOYSA-N 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 238000005562 fading Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229920006178 high molecular weight high density polyethylene Polymers 0.000 description 2
- 125000001841 imino group Chemical group [H]N=* 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 229910052749 magnesium Inorganic materials 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
- 239000000463 material Substances 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- UKJARPDLRWBRAX-UHFFFAOYSA-N n,n'-bis(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound C1C(C)(C)NC(C)(C)CC1NCCCCCCNC1CC(C)(C)NC(C)(C)C1 UKJARPDLRWBRAX-UHFFFAOYSA-N 0.000 description 2
- BLBLVDQTHWVGRA-UHFFFAOYSA-N n-butyl-3-[4-[4-(butylamino)-1,2,2,6,6-pentamethylpiperidin-3-yl]-6-chloro-1,3,5-triazin-2-yl]-1,2,2,6,6-pentamethylpiperidin-4-amine Chemical compound CCCCNC1CC(C)(C)N(C)C(C)(C)C1C1=NC(Cl)=NC(C2C(N(C)C(C)(C)CC2NCCCC)(C)C)=N1 BLBLVDQTHWVGRA-UHFFFAOYSA-N 0.000 description 2
- SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical compound ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 description 2
- RQVGZVZFVNMBGS-UHFFFAOYSA-N n-octyl-n-phenylaniline Chemical class C=1C=CC=CC=1N(CCCCCCCC)C1=CC=CC=C1 RQVGZVZFVNMBGS-UHFFFAOYSA-N 0.000 description 2
- 150000002815 nickel Chemical class 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 238000006384 oligomerization reaction Methods 0.000 description 2
- 125000003431 oxalo group Chemical group 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- 150000003003 phosphines Chemical class 0.000 description 2
- 150000008301 phosphite esters Chemical class 0.000 description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920001228 polyisocyanate Polymers 0.000 description 2
- 239000005056 polyisocyanate Substances 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000005060 rubber Substances 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
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 235000012222 talc Nutrition 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
- 239000011732 tocopherol Substances 0.000 description 2
- 229960001295 tocopherol Drugs 0.000 description 2
- DUXYWXYOBMKGIN-UHFFFAOYSA-N trimyristin Chemical compound CCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCC DUXYWXYOBMKGIN-UHFFFAOYSA-N 0.000 description 2
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 2
- 150000003751 zinc Chemical class 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 2
- OUBISKKOUYNDML-UHFFFAOYSA-N (2,2,6,6-tetramethylpiperidin-4-yl) 2-[bis[2-oxo-2-(2,2,6,6-tetramethylpiperidin-4-yl)oxyethyl]amino]acetate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CN(CC(=O)OC1CC(C)(C)NC(C)(C)C1)CC(=O)OC1CC(C)(C)NC(C)(C)C1 OUBISKKOUYNDML-UHFFFAOYSA-N 0.000 description 1
- HQEPZWYPQQKFLU-UHFFFAOYSA-N (2,6-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC(O)=C1C(=O)C1=CC=CC=C1 HQEPZWYPQQKFLU-UHFFFAOYSA-N 0.000 description 1
- HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical compound OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 1
- WOULRINQDJQFMX-UHFFFAOYSA-N (2-phosphanylphenyl)methanamine Chemical compound NCC1=CC=CC=C1P WOULRINQDJQFMX-UHFFFAOYSA-N 0.000 description 1
- ZIJHTQPOUJBOHK-UHFFFAOYSA-N (3-tert-butyl-4-hydroxy-5-methylphenyl)methylphosphonic acid Chemical class CC1=CC(CP(O)(O)=O)=CC(C(C)(C)C)=C1O ZIJHTQPOUJBOHK-UHFFFAOYSA-N 0.000 description 1
- BEVYLNVECSORPM-UHFFFAOYSA-N (4-phosphanylphenyl)methanamine Chemical compound NCC1=CC=C(P)C=C1 BEVYLNVECSORPM-UHFFFAOYSA-N 0.000 description 1
- GOZHNJTXLALKRL-UHFFFAOYSA-N (5-benzoyl-2,4-dihydroxyphenyl)-phenylmethanone Chemical compound OC1=CC(O)=C(C(=O)C=2C=CC=CC=2)C=C1C(=O)C1=CC=CC=C1 GOZHNJTXLALKRL-UHFFFAOYSA-N 0.000 description 1
- 125000006558 (C6-C8) cycloalkyl group Chemical group 0.000 description 1
- CGXOAAMIQPDTPE-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidin-4-amine Chemical class CN1C(C)(C)CC(N)CC1(C)C CGXOAAMIQPDTPE-UHFFFAOYSA-N 0.000 description 1
- XULIXFLCVXWHRF-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidine Chemical class CN1C(C)(C)CCCC1(C)C XULIXFLCVXWHRF-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- JEFSTMHERNSDBC-UHFFFAOYSA-N 1,2-dimethylcyclohexa-2,4-dien-1-ol Chemical compound CC1=CC=CCC1(C)O JEFSTMHERNSDBC-UHFFFAOYSA-N 0.000 description 1
- JDLQSLMTBGPZLW-UHFFFAOYSA-N 1-(1-hydroxyethyl)-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC(O)N1C(C)(C)CC(O)CC1(C)C JDLQSLMTBGPZLW-UHFFFAOYSA-N 0.000 description 1
- PPNDFSTWANYHQM-UHFFFAOYSA-N 1-(3-amino-4-hydroxyphenyl)dodecan-1-one Chemical compound CCCCCCCCCCCC(=O)C1=CC=C(O)C(N)=C1 PPNDFSTWANYHQM-UHFFFAOYSA-N 0.000 description 1
- UDAKRDQBQXLJHF-UHFFFAOYSA-N 1-(3-amino-4-hydroxyphenyl)nonan-1-one Chemical compound CCCCCCCCC(=O)C1=CC=C(O)C(N)=C1 UDAKRDQBQXLJHF-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- PWNBRRGFUVBTQG-UHFFFAOYSA-N 1-n,4-n-di(propan-2-yl)benzene-1,4-diamine Chemical compound CC(C)NC1=CC=C(NC(C)C)C=C1 PWNBRRGFUVBTQG-UHFFFAOYSA-N 0.000 description 1
- AIMXDOGPMWDCDF-UHFFFAOYSA-N 1-n,4-n-dicyclohexylbenzene-1,4-diamine Chemical compound C1CCCCC1NC(C=C1)=CC=C1NC1CCCCC1 AIMXDOGPMWDCDF-UHFFFAOYSA-N 0.000 description 1
- HGIKZZLUIDRDRG-UHFFFAOYSA-N 2,2,6,6-tetramethyl-1-octoxypiperidine Chemical compound CCCCCCCCON1C(C)(C)CCCC1(C)C HGIKZZLUIDRDRG-UHFFFAOYSA-N 0.000 description 1
- ADVWVIQNAOXLCV-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperazine Chemical compound CC1(C)CNCC(C)(C)N1 ADVWVIQNAOXLCV-UHFFFAOYSA-N 0.000 description 1
- IMJPDWLPOLPEAY-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;propanoic acid Chemical class CCC(O)=O.OCC(CO)(CO)CO IMJPDWLPOLPEAY-UHFFFAOYSA-N 0.000 description 1
- LXUNZSDDXMPKLP-UHFFFAOYSA-N 2-Methylbenzenethiol Chemical compound CC1=CC=CC=C1S LXUNZSDDXMPKLP-UHFFFAOYSA-N 0.000 description 1
- UTNMPUFESIRPQP-UHFFFAOYSA-N 2-[(4-aminophenyl)methyl]aniline Chemical compound C1=CC(N)=CC=C1CC1=CC=CC=C1N UTNMPUFESIRPQP-UHFFFAOYSA-N 0.000 description 1
- OCDFZRIOTQBMDV-UHFFFAOYSA-N 2-amino-4-octadecylphenol Chemical compound CCCCCCCCCCCCCCCCCCC1=CC=C(O)C(N)=C1 OCDFZRIOTQBMDV-UHFFFAOYSA-N 0.000 description 1
- KDHONNUUDHJCID-UHFFFAOYSA-N 2-cyclopentyl-4-methylphenol Chemical class CC1=CC=C(O)C(C2CCCC2)=C1 KDHONNUUDHJCID-UHFFFAOYSA-N 0.000 description 1
- MYUNWHTZYXUCIK-UHFFFAOYSA-N 2-methanehydrazonoylphenol Chemical compound NN=CC1=CC=CC=C1O MYUNWHTZYXUCIK-UHFFFAOYSA-N 0.000 description 1
- VSKJLJHPAFKHBX-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1.C=CC1=CC=CC=C1 VSKJLJHPAFKHBX-UHFFFAOYSA-N 0.000 description 1
- JMMZCWZIJXAGKW-UHFFFAOYSA-N 2-methylpent-2-ene Chemical compound CCC=C(C)C JMMZCWZIJXAGKW-UHFFFAOYSA-N 0.000 description 1
- ZFMFIBDSZCASNS-UHFFFAOYSA-N 2-pentylbenzene-1,4-diol Chemical compound CCCCCC1=CC(O)=CC=C1O ZFMFIBDSZCASNS-UHFFFAOYSA-N 0.000 description 1
- DHKGWJHJJZJZGD-UHFFFAOYSA-N 2-tert-butyl-4-(2-methylpropyl)phenol Chemical compound CC(C)CC1=CC=C(O)C(C(C)(C)C)=C1 DHKGWJHJJZJZGD-UHFFFAOYSA-N 0.000 description 1
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical class CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 description 1
- UCSGVHDXJLPMQV-UHFFFAOYSA-N 3-(4-hydroxyphenyl)-2-sulfanylpropanoic acid Chemical compound OC(=O)C(S)CC1=CC=C(O)C=C1 UCSGVHDXJLPMQV-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- UQAMDAUJTXFNAD-UHFFFAOYSA-N 4-(4,6-dichloro-1,3,5-triazin-2-yl)morpholine Chemical compound ClC1=NC(Cl)=NC(N2CCOCC2)=N1 UQAMDAUJTXFNAD-UHFFFAOYSA-N 0.000 description 1
- OILMLWAZYNVPMG-UHFFFAOYSA-N 4-methyl-2-nonylphenol Chemical class CCCCCCCCCC1=CC(C)=CC=C1O OILMLWAZYNVPMG-UHFFFAOYSA-N 0.000 description 1
- NTDQQZYCCIDJRK-UHFFFAOYSA-N 4-octylphenol Chemical compound CCCCCCCCC1=CC=C(O)C=C1 NTDQQZYCCIDJRK-UHFFFAOYSA-N 0.000 description 1
- BVNWQSXXRMNYKH-UHFFFAOYSA-N 4-phenyl-2h-benzotriazole Chemical compound C1=CC=CC=C1C1=CC=CC2=C1NN=N2 BVNWQSXXRMNYKH-UHFFFAOYSA-N 0.000 description 1
- UTPKNSJKAVUAOA-UHFFFAOYSA-N 5,7-ditert-butyl-3-phenyl-3h-1-benzofuran-2-one Chemical class O=C1OC=2C(C(C)(C)C)=CC(C(C)(C)C)=CC=2C1C1=CC=CC=C1 UTPKNSJKAVUAOA-UHFFFAOYSA-N 0.000 description 1
- PZBQVZFITSVHAW-UHFFFAOYSA-N 5-chloro-2h-benzotriazole Chemical compound C1=C(Cl)C=CC2=NNN=C21 PZBQVZFITSVHAW-UHFFFAOYSA-N 0.000 description 1
- OJOWICOBYCXEKR-UHFFFAOYSA-N 5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical group C1C2C(=CC)CC1C=C2 OJOWICOBYCXEKR-UHFFFAOYSA-N 0.000 description 1
- ULRUZVQNSYMOPS-UHFFFAOYSA-N 5-methyl-2-undecylphenol Chemical compound CCCCCCCCCCCC1=CC=C(C)C=C1O ULRUZVQNSYMOPS-UHFFFAOYSA-N 0.000 description 1
- VPOKLVDHXARWQB-UHFFFAOYSA-N 7,7,9,9-tetramethyl-3-octyl-1,3,8-triazaspiro[4.5]decane-2,4-dione Chemical compound O=C1N(CCCCCCCC)C(=O)NC11CC(C)(C)NC(C)(C)C1 VPOKLVDHXARWQB-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- 229940123208 Biguanide Drugs 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- ODIZQISMRSWNQK-UHFFFAOYSA-N C(C1=CC=C(C(=O)O)C=C1)(=O)O.[S] Chemical class C(C1=CC=C(C(=O)O)C=C1)(=O)O.[S] ODIZQISMRSWNQK-UHFFFAOYSA-N 0.000 description 1
- GHFPUMWUXFDVEQ-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)(=O)C1C(C(N(CC1)C)(C)C)(C)C Chemical compound C(CCCCCCCCCCCCCCCCC)(=O)C1C(C(N(CC1)C)(C)C)(C)C GHFPUMWUXFDVEQ-UHFFFAOYSA-N 0.000 description 1
- IWVFKMHEMOCFPE-UHFFFAOYSA-N CCCCCCCCCCCCC.C(C1=CC=CC=C1)C(C(=O)O)S Chemical class CCCCCCCCCCCCC.C(C1=CC=CC=C1)C(C(=O)O)S IWVFKMHEMOCFPE-UHFFFAOYSA-N 0.000 description 1
- ZILTZGFQHFMQLH-UHFFFAOYSA-N COP(O)=O.CC(C1=CC=CC=C1)(C)C Chemical class COP(O)=O.CC(C1=CC=CC=C1)(C)C ZILTZGFQHFMQLH-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
- GNNPJZUDJSDYRK-UHFFFAOYSA-N ClC1=CC=2C(=NN(N2)C2=C(C(=CC(=C2)CN)C(C)(C)C)O)C=C1 Chemical compound ClC1=CC=2C(=NN(N2)C2=C(C(=CC(=C2)CN)C(C)(C)C)O)C=C1 GNNPJZUDJSDYRK-UHFFFAOYSA-N 0.000 description 1
- 229910020366 ClO 4 Inorganic materials 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- 229920000089 Cyclic olefin copolymer Chemical group 0.000 description 1
- 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 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 description 1
- 229920001174 Diethylhydroxylamine Polymers 0.000 description 1
- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 1
- VURFVHCLMJOLKN-UHFFFAOYSA-N Diphosphine Natural products PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 description 1
- 239000002656 Distearyl thiodipropionate Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- IYXGSMUGOJNHAZ-UHFFFAOYSA-N Ethyl malonate Chemical compound CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 description 1
- 239000004812 Fluorinated ethylene propylene Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- VHOQXEIFYTTXJU-UHFFFAOYSA-N Isobutylene-isoprene copolymer Chemical compound CC(C)=C.CC(=C)C=C VHOQXEIFYTTXJU-UHFFFAOYSA-N 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Natural products CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- ZVSQSTFEGWYEQA-UHFFFAOYSA-N N-ethyl-6-(2,2,6,6-tetramethylpiperidin-4-yl)iminohexan-1-amine Chemical compound CC1(NC(CC(C1)N=CCCCCCNCC)(C)C)C ZVSQSTFEGWYEQA-UHFFFAOYSA-N 0.000 description 1
- WCGXJIOTELBXHF-UHFFFAOYSA-N N1=CN=CN=C1.CC1=CC=CC(=C1)C Chemical class N1=CN=CN=C1.CC1=CC=CC(=C1)C WCGXJIOTELBXHF-UHFFFAOYSA-N 0.000 description 1
- JHXVRRJXCDAINK-UHFFFAOYSA-N NC(=O)N.N#CC#N Chemical compound NC(=O)N.N#CC#N JHXVRRJXCDAINK-UHFFFAOYSA-N 0.000 description 1
- ZWZOGCLCGHHRSO-UHFFFAOYSA-N NC1CCC(CC1)C1=NC(=NC(=N1)Cl)Cl Chemical compound NC1CCC(CC1)C1=NC(=NC(=N1)Cl)Cl ZWZOGCLCGHHRSO-UHFFFAOYSA-N 0.000 description 1
- ISPIYAIQOFAEGX-UHFFFAOYSA-N NO.CCCCCCCCCCCCCC Chemical class NO.CCCCCCCCCCCCCC ISPIYAIQOFAEGX-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- HXHOTMRIMKEHGZ-UHFFFAOYSA-N OC(C[O])C.[O] Chemical compound OC(C[O])C.[O] HXHOTMRIMKEHGZ-UHFFFAOYSA-N 0.000 description 1
- IWGBGUINMSOOKP-UHFFFAOYSA-N OC1=C(C(=O)CCCCCCCCCCC)C=NN1C1=CC=CC=C1 Chemical class OC1=C(C(=O)CCCCCCCCCCC)C=NN1C1=CC=CC=C1 IWGBGUINMSOOKP-UHFFFAOYSA-N 0.000 description 1
- GNHGKMNJKZCSTM-UHFFFAOYSA-N OCC(CO)(CO)CO.C(CCCCCCC(C)C)[O] Chemical class OCC(CO)(CO)CO.C(CCCCCCC(C)C)[O] GNHGKMNJKZCSTM-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- KJLGNARPBNIKGZ-UHFFFAOYSA-N P.P.C1=CC=CC=C1 Chemical class P.P.C1=CC=CC=C1 KJLGNARPBNIKGZ-UHFFFAOYSA-N 0.000 description 1
- 229920007019 PC/ABS Polymers 0.000 description 1
- 229920006778 PC/PBT Polymers 0.000 description 1
- 239000005591 Pendimethalin Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004693 Polybenzimidazole Substances 0.000 description 1
- 229920003006 Polybutadiene acrylonitrile Polymers 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004697 Polyetherimide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 1
- 240000000203 Salix gracilistyla Species 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910004283 SiO 4 Inorganic materials 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 1
- 239000003490 Thiodipropionic acid Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- YEAUKDXLSZWZRU-UHFFFAOYSA-N [O].CC1(NC(CCC1)(C)C)C Chemical compound [O].CC1(NC(CCC1)(C)C)C YEAUKDXLSZWZRU-UHFFFAOYSA-N 0.000 description 1
- INKDAKMSOSCDGL-UHFFFAOYSA-N [O].OC1=CC=CC=C1 Chemical compound [O].OC1=CC=CC=C1 INKDAKMSOSCDGL-UHFFFAOYSA-N 0.000 description 1
- YSFVDVZOGIPGEU-UHFFFAOYSA-N [Sb].OC1=CC=CC=C1O Chemical compound [Sb].OC1=CC=CC=C1O YSFVDVZOGIPGEU-UHFFFAOYSA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- OLFJVIXNILIZKF-UHFFFAOYSA-N acetic acid;sodium Chemical compound [Na].CC(O)=O.CC(O)=O OLFJVIXNILIZKF-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229940087168 alpha tocopherol Drugs 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 159000000013 aluminium salts Chemical class 0.000 description 1
- 229910000329 aluminium sulfate Inorganic materials 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 125000000477 aza group Chemical group 0.000 description 1
- 125000002648 azanetriyl group Chemical group *N(*)* 0.000 description 1
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 229910052728 basic metal Inorganic materials 0.000 description 1
- 150000003818 basic metals Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- IRSWRCCZAUZIMU-UHFFFAOYSA-N benzene-1,2-diol;tin Chemical compound [Sn].OC1=CC=CC=C1O IRSWRCCZAUZIMU-UHFFFAOYSA-N 0.000 description 1
- YAVVGPBYBUYPSR-UHFFFAOYSA-N benzene;oxygen Chemical compound [O].C1=CC=CC=C1 YAVVGPBYBUYPSR-UHFFFAOYSA-N 0.000 description 1
- QICVZJNIJUZAGZ-UHFFFAOYSA-N benzene;phosphorous acid Chemical compound OP(O)O.C1=CC=CC=C1 QICVZJNIJUZAGZ-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- CUBCNYWQJHBXIY-UHFFFAOYSA-N benzoic acid;2-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=CC=C1.OC(=O)C1=CC=CC=C1O CUBCNYWQJHBXIY-UHFFFAOYSA-N 0.000 description 1
- 150000004283 biguanides Chemical class 0.000 description 1
- RYROHTOBUZBHFG-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-3-yl) 2-butyl-2-[(3,5-ditert-butyl-2-hydroxyphenyl)methyl]propanedioate Chemical compound C1CC(C)(C)N(C)C(C)(C)C1OC(=O)C(C(=O)OC1C(N(C)C(C)(C)CC1)(C)C)(CCCC)CC1=CC(C(C)(C)C)=CC(C(C)(C)C)=C1O RYROHTOBUZBHFG-UHFFFAOYSA-N 0.000 description 1
- MJMDMGXKEGBVKR-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-3-yl) 2-butyl-2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]propanedioate Chemical compound C1CC(C)(C)N(C)C(C)(C)C1OC(=O)C(C(=O)OC1C(N(C)C(C)(C)CC1)(C)C)(CCCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 MJMDMGXKEGBVKR-UHFFFAOYSA-N 0.000 description 1
- GOJOVSYIGHASEI-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) butanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCC(=O)OC1CC(C)(C)NC(C)(C)C1 GOJOVSYIGHASEI-UHFFFAOYSA-N 0.000 description 1
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 1
- YTCAGGVGRNNAHU-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) pentanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCC(=O)OC1CC(C)(C)NC(C)(C)C1 YTCAGGVGRNNAHU-UHFFFAOYSA-N 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- XUCHXOAWJMEFLF-UHFFFAOYSA-N bisphenol F diglycidyl ether Chemical compound C1OC1COC(C=C1)=CC=C1CC(C=C1)=CC=C1OCC1CO1 XUCHXOAWJMEFLF-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 239000001405 butyl (E)-3-phenylprop-2-enoate Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 229920006218 cellulose propionate Polymers 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 150000001925 cycloalkenes Chemical class 0.000 description 1
- 150000001941 cyclopentenes Chemical class 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzylether Substances C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- YLFBFPXKTIQSSY-UHFFFAOYSA-N dimethoxy(oxo)phosphanium Chemical compound CO[P+](=O)OC YLFBFPXKTIQSSY-UHFFFAOYSA-N 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- QTZWEOORJXECRA-UHFFFAOYSA-N diphenylphosphane ethylbenzene Chemical compound CCC1=CC=CC=C1.C1(=CC=CC=C1)PC1=CC=CC=C1 QTZWEOORJXECRA-UHFFFAOYSA-N 0.000 description 1
- AJJZBOFUSXFCSG-UHFFFAOYSA-N diphenylphosphane;octane Chemical class CCCCCCCC.C=1C=CC=CC=1PC1=CC=CC=C1 AJJZBOFUSXFCSG-UHFFFAOYSA-N 0.000 description 1
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 description 1
- 235000019305 distearyl thiodipropionate Nutrition 0.000 description 1
- SNRUBQQJIBEYMU-NJFSPNSNSA-N dodecane Chemical class CCCCCCCCCCC[14CH3] SNRUBQQJIBEYMU-NJFSPNSNSA-N 0.000 description 1
- 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 1
- 229940091854 dodecyl propionate Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000010696 ester oil Substances 0.000 description 1
- HEAMQYHBJQWOSS-UHFFFAOYSA-N ethene;oct-1-ene Chemical compound C=C.CCCCCCC=C HEAMQYHBJQWOSS-UHFFFAOYSA-N 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 1
- UXCMPJDXZLKVBA-UHFFFAOYSA-N ethylphosphane propane Chemical compound CCC.C(C)P UXCMPJDXZLKVBA-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 235000010382 gamma-tocopherol Nutrition 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 229920005555 halobutyl Polymers 0.000 description 1
- 125000004968 halobutyl group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- AHAREKHAZNPPMI-UHFFFAOYSA-N hexa-1,3-diene Chemical compound CCC=CC=C AHAREKHAZNPPMI-UHFFFAOYSA-N 0.000 description 1
- ACKXLKCWSICXRB-UHFFFAOYSA-N hexadecane hydroxylamine Chemical class NO.CCCCCCCCCCCCCCCC ACKXLKCWSICXRB-UHFFFAOYSA-N 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N hexanedioic acid Natural products OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 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
- 229920005669 high impact polystyrene Polymers 0.000 description 1
- 239000004797 high-impact polystyrene Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- PEASJMCUUTZGHV-UHFFFAOYSA-N hydroxylamine octadecane Chemical class NO.CCCCCCCCCCCCCCCCCC PEASJMCUUTZGHV-UHFFFAOYSA-N 0.000 description 1
- 230000033444 hydroxylation Effects 0.000 description 1
- 238000005805 hydroxylation reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 239000008141 laxative Substances 0.000 description 1
- 230000002475 laxative effect Effects 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 235000012204 lemonade/lime carbonate Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229960003511 macrogol Drugs 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052987 metal hydride Inorganic materials 0.000 description 1
- 150000004681 metal hydrides Chemical class 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 1
- UJRDRFZCRQNLJM-UHFFFAOYSA-N methyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OC)=CC(N2N=C3C=CC=CC3=N2)=C1O UJRDRFZCRQNLJM-UHFFFAOYSA-N 0.000 description 1
- 125000006178 methyl benzyl group Chemical group 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- GXFQBBOZTNQHMW-UHFFFAOYSA-N n'-(2,2,6,6-tetramethylpiperidin-4-yl)hexane-1,6-diamine Chemical compound CC1(C)CC(NCCCCCCN)CC(C)(C)N1 GXFQBBOZTNQHMW-UHFFFAOYSA-N 0.000 description 1
- YIMHRDBSVCPJOV-UHFFFAOYSA-N n'-(2-ethoxyphenyl)-n-(2-ethylphenyl)oxamide Chemical compound CCOC1=CC=CC=C1NC(=O)C(=O)NC1=CC=CC=C1CC YIMHRDBSVCPJOV-UHFFFAOYSA-N 0.000 description 1
- BTYJSJKBQMQWHD-UHFFFAOYSA-N n'-[2-[2-(2-aminoethylamino)ethylamino]ethyl]ethane-1,2-diamine;n'-[2-(2-aminoethylamino)ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCN.NCCNCCNCCNCCN BTYJSJKBQMQWHD-UHFFFAOYSA-N 0.000 description 1
- GXELTROTKVKZBQ-UHFFFAOYSA-N n,n-dibenzylhydroxylamine Chemical compound C=1C=CC=CC=1CN(O)CC1=CC=CC=C1 GXELTROTKVKZBQ-UHFFFAOYSA-N 0.000 description 1
- DHXOCDLHWYUUAG-UHFFFAOYSA-N n,n-didodecylhydroxylamine Chemical compound CCCCCCCCCCCCN(O)CCCCCCCCCCCC DHXOCDLHWYUUAG-UHFFFAOYSA-N 0.000 description 1
- WQAJFRSBFZAUPB-UHFFFAOYSA-N n,n-dioctylhydroxylamine Chemical compound CCCCCCCCN(O)CCCCCCCC WQAJFRSBFZAUPB-UHFFFAOYSA-N 0.000 description 1
- KESXDDATSRRGAH-UHFFFAOYSA-N n-(4-hydroxyphenyl)butanamide Chemical compound CCCC(=O)NC1=CC=C(O)C=C1 KESXDDATSRRGAH-UHFFFAOYSA-N 0.000 description 1
- AXMMDKIETYVDGR-UHFFFAOYSA-N n-[6-[formyl-(1,2,2,6,6-pentamethylpiperidin-4-yl)amino]hexyl]-n-(1,2,2,6,6-pentamethylpiperidin-4-yl)formamide Chemical compound C1C(C)(C)N(C)C(C)(C)CC1N(C=O)CCCCCCN(C=O)C1CC(C)(C)N(C)C(C)(C)C1 AXMMDKIETYVDGR-UHFFFAOYSA-N 0.000 description 1
- FDAKZQLBIFPGSV-UHFFFAOYSA-N n-butyl-2,2,6,6-tetramethylpiperidin-4-amine Chemical compound CCCCNC1CC(C)(C)NC(C)(C)C1 FDAKZQLBIFPGSV-UHFFFAOYSA-N 0.000 description 1
- LRUUZFQPCUFYPV-UHFFFAOYSA-N n-dodecyldodecan-1-imine oxide Chemical compound CCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCC LRUUZFQPCUFYPV-UHFFFAOYSA-N 0.000 description 1
- GBMIPYGHTZRCRH-UHFFFAOYSA-N n-ethylethanimine oxide Chemical compound CC[N+]([O-])=CC GBMIPYGHTZRCRH-UHFFFAOYSA-N 0.000 description 1
- DBCWENWKZARTGU-UHFFFAOYSA-N n-heptadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC=[N+]([O-])CCCCCCCCCCCCCCCCC DBCWENWKZARTGU-UHFFFAOYSA-N 0.000 description 1
- GCDJFNYVSDFWDB-UHFFFAOYSA-N n-hexadecylhexadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCC GCDJFNYVSDFWDB-UHFFFAOYSA-N 0.000 description 1
- FHAFFFSIDLDWQA-UHFFFAOYSA-N n-hexadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC=[N+]([O-])CCCCCCCCCCCCCCCC FHAFFFSIDLDWQA-UHFFFAOYSA-N 0.000 description 1
- ZXGDIORKSOYRMQ-UHFFFAOYSA-N n-octadecylheptadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCCC ZXGDIORKSOYRMQ-UHFFFAOYSA-N 0.000 description 1
- MCMMSXFAWOGWQE-UHFFFAOYSA-N n-octadecylhexadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCC MCMMSXFAWOGWQE-UHFFFAOYSA-N 0.000 description 1
- HORBOHJHQGXXOR-UHFFFAOYSA-N n-octadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCCCCCC HORBOHJHQGXXOR-UHFFFAOYSA-N 0.000 description 1
- ZOLJFBQEKSZVCB-UHFFFAOYSA-N n-phenyloctadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NC1=CC=CC=C1 ZOLJFBQEKSZVCB-UHFFFAOYSA-N 0.000 description 1
- CDZOGLJOFWFVOZ-UHFFFAOYSA-N n-propylaniline Chemical compound CCCNC1=CC=CC=C1 CDZOGLJOFWFVOZ-UHFFFAOYSA-N 0.000 description 1
- SLYJXPKHTZCZOG-UHFFFAOYSA-N n-tetradecyltetradecan-1-imine oxide Chemical compound CCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCC SLYJXPKHTZCZOG-UHFFFAOYSA-N 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 150000002816 nickel compounds Chemical class 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- 125000005574 norbornylene group Chemical group 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000005461 organic phosphorous group Chemical group 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920009441 perflouroethylene propylene Polymers 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- ZPNJBTBYIHBSIG-UHFFFAOYSA-N phenyl-(2,2,6,6-tetramethylpiperidin-4-yl)methanone Chemical compound C1C(C)(C)NC(C)(C)CC1C(=O)C1=CC=CC=C1 ZPNJBTBYIHBSIG-UHFFFAOYSA-N 0.000 description 1
- HKOOXMFOFWEVGF-UHFFFAOYSA-N phenylhydrazine Chemical compound NNC1=CC=CC=C1 HKOOXMFOFWEVGF-UHFFFAOYSA-N 0.000 description 1
- BCIKIEREBOMXRL-UHFFFAOYSA-N phosphocine Chemical compound C1=CC=CP=CC=C1 BCIKIEREBOMXRL-UHFFFAOYSA-N 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 239000012994 photoredox catalyst Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920003251 poly(α-methylstyrene) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002480 polybenzimidazole Polymers 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920001444 polymaleic acid Polymers 0.000 description 1
- 238000012667 polymer degradation Methods 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- MQOCIYICOGDBSG-UHFFFAOYSA-M potassium;hexadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCC([O-])=O MQOCIYICOGDBSG-UHFFFAOYSA-M 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 229940074404 sodium succinate Drugs 0.000 description 1
- JMHCCAYJTTWMCX-QWPJCUCISA-M sodium;(2s)-2-amino-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]propanoate;pentahydrate Chemical compound O.O.O.O.O.[Na+].IC1=CC(C[C@H](N)C([O-])=O)=CC(I)=C1OC1=CC(I)=C(O)C(I)=C1 JMHCCAYJTTWMCX-QWPJCUCISA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000003351 stiffener Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000005987 sulfurization reaction Methods 0.000 description 1
- 239000012747 synergistic agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 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
- NZNAAUDJKMURFU-UHFFFAOYSA-N tetrakis(2,2,6,6-tetramethylpiperidin-4-yl) butane-1,2,3,4-tetracarboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CC(C(=O)OC1CC(C)(C)NC(C)(C)C1)C(C(=O)OC1CC(C)(C)NC(C)(C)C1)CC(=O)OC1CC(C)(C)NC(C)(C)C1 NZNAAUDJKMURFU-UHFFFAOYSA-N 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 239000012745 toughening agent Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 230000003245 working effect Effects 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
- WGVKWNUPNGFDFJ-DQCZWYHMSA-N β-tocopherol Chemical compound OC1=CC(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C WGVKWNUPNGFDFJ-DQCZWYHMSA-N 0.000 description 1
- 239000002478 γ-tocopherol Substances 0.000 description 1
- QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-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
- C08K5/49—Phosphorus-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- 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
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
- C08K5/3432—Six-membered rings
- C08K5/3435—Piperidines
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)
- Artificial Filaments (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Road Paving Structures (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
本发明涉及用于热塑性聚合物的稳定剂组合物,包含a)至少一种有机膦,b)至少一种2-苯基苯并呋喃酮,及c)至少一种基于空间位阻哌啶的稳定剂(HAS),其中成分a)对成分b)对成分c)的重量比为从1∶0.05∶0.5到1∶3∶5。本组合物的总浓度低于传统的酚类制剂。本制剂能避免聚烯烃制品(尤指聚烯烃纤维)在加工及使用时因形成醌型产物及受到NOx气体的作用(气体褪色)而褪色。
Description
本发明涉及不含酚类抗氧化剂的聚烯烃(尤其聚丙烯PP)的稳定化组合物。
聚烯烃制品,尤其是聚烯烃纤维,是要成功地应用合成原材料而需进行稳定化的最典型例子。聚丙烯在其整个使用期间均须防护。特别是聚丙烯纤维通常要求在比其他聚丙烯制品更高的温度下(典型的是270~300℃)进行加工,故需专门注意。
通常的稳定化制剂由酚类抗氧化剂与有机亚磷酸酯和亚膦酸酯联合使用而组成,以提供足够的加工稳定性,并确保对热氧化降解的长期防护作用。然而亚磷酸酯及亚膦酸酯对于抗氧化并无显著的贡献。
多年来由文献可知,基于哌啶的稳定剂(HAS),尤其是高分子量HAS对于聚丙烯有长期热防护作用。通常聚丙烯纤维的损坏时间随着HAS浓度的提升而以非线性方式延长。
另一方面,已被熟知的是,含有作为长期热防护用的主抗氧化剂的空间位阻酚类抗氧化剂的聚合物发生褪色是因为形成了这些添加剂的具有醌型结构的有色转移产物。其程度依赖于酚的结构和用量。通常连续的接触水或氮氧化物气体时,聚烯烃的褪色特别显著[参阅F.Gugumus,塑料添加剂的“抗氧化剂”一节,R.Gchter和H.Müller编,Hanser出版社,慕尼黑,维也纳,纽约,第3版,1-104页,1990年;及P.P.Klemchuk和P.L.Horng,“聚合物降解稳定化”,卷34,333页,1991年]。
这些作用及现象引来了新的稳定化技术方案,使得在聚烯烃尤其是聚丙烯纤维的稳定化中放弃空间位阻酚。如今新一代的稳定剂已经商品化,其可实现用于制造聚丙烯纤维的高温加工。
已知的无酚稳定化系统由有机亚磷(膦)酸酯、基于苯并呋喃酮的成分和基于哌啶的HAS化合物组成。英国专利GB-A-2,315,070公开了有机材料的稳定化混合物,包含至少一种苯并呋喃-2-酮型化合物及至少一种空间位阻胺型化合物,此稳定化混合物中也可含有有机亚磷酸酯或亚膦酸酯。
本发明的目的是提供用于稳定聚烯烃聚合物的改良稳定剂组合物,其中酚类抗氧化剂并非必需的。
由下述的稳定剂组合物即可实现此目的。如今我们已发现按照下述特定的比例采用适当的无酚稳定剂系统,即能符合聚烯烃加工,特别是聚烯烃纤维加工的技术要求,和传统的含酚稳定剂制剂比较起来,在维持分子量及颜色方面都有显著的改良。
这些添加剂系统基本上由有机膦,2-苯基苯并呋喃酮(内酯)及基于空间位阻哌啶的稳定剂(HAS)所组成。
于是本发明提供稳定剂组合物,包含
a)至少一种有机膦,
b)至少一种2-苯基苯并呋喃酮,及
c)至少一种基于空间位阻哌啶的稳定剂(HAS),
其中成分a)对成分b)对成分c)的重量比为从1∶0.05∶0.5至1∶3∶5。
优选地本发明提供的稳定剂组合物包含
a)至少一种式(I)至(IV)的化合物[以下称之为成分a]
其中各自独立的,
R1是C1-24烷基或C1-24-N,O,P,S-杂烷基;C5-30环烷基或C5-30-N,O,P,S-杂环烷基;C7-30烷芳基;C6-24芳基;C4-24-N,O,P,S-杂芳基;C6-24芳基或被C1-18烷基,C5-12环烷基或C1-18烷氧基所单-或多-取代的C4-24-N,O,P,S-杂芳基;
R2是C4-24烷基或C4-24-N,O,P,S-杂烷基;C5-30环烷基或C5-30- N,O,P,S-杂环烷基;C7-30烷芳基;C6-24芳基;C4-24-N,O,P,S-杂芳基;C6-24芳基或被C1-18烷基,C5-12环烷基或C1-18烷氧基所单-或多-取代的C4-24-N,O,P,S-杂芳基;
D是直链或支链的C1-30亚烷基或C1-30-N,O,P,S-亚烷基;C2-30烷叉基或C2-30-N,O,P,S-烷叉基;C5-12亚环烷基或C5-12-N,O,P,S-亚环烷基;未被取代的或被直链或支链的C1-18烷基,C5-12环烷基或C1-18烷氧基所单-或多-取代的C6-24亚芳基或C4-24-N,O,P,S-亚杂芳基;或-O-,-S-;
q是1至5;
r是3至6,当式(IV)中的P-R1基团是磷杂环的成分时,以由P引出的键中的*号表示;
b)至少一种式(V)的化合物(称之为成分b):
其中Ra、Rb、Rd、Re、Rf、Rg及Rh各自独立的为氢、羟基;C1-18烷基、或未取代的或被C1-4烷基所单-、双-或三-取代的苯基;未被取代或被C1-4烷基所单-、双-或三-取代的C7-9苯烷基、C1-18烷氧基或C5-12环烷基;而Re如前面Ra、Rb、Rd、Re、Rf、Rg和Rh的定义,或是式(VI)的基团:
其中Ra、Rb、Rd、Re、Rf、Rg及Rh如前面所定义,和Ri、Rj各自独立的为氢或C1-4烷基,和在Rd、Re、Rf、Rg和Rh中至少有两个是氢;和
c)至少一种式VII的空间位阻胺(称之为成分c):
其中X1是氢,C1-22烷基;氧自由基O*;-OH;-NO;-CH2CN;苄基;烯丙基;C1-30烷氧基;C5-12环烷氧基;C6-10芳氧基;C7-20芳烷氧基或其中芳基被C1-5烷基,卤原子或硝基所取代的C7-20芳烷氧基;C3-10烯基;C3-6炔基;C1-10酰基;卤原子;未被取代或被C1-4烷基取代的苯基;
X2是氢、[CH2-CH2-C(O)-O-X5]基;[CH2-C(CH3)H-C(O)-O-X5]基;C1-22烷基;
X3及X4各自独立地为氢、未被取代或被C1-4烷基取代的苯基;或C1-22烷基,其中X3及X4中至少有一个为支链的C4-22烷基;和其中
X5是C1-22烷基。
前述的烷基可呈直链或支链。
优选的成分中:
R1是C8-24烷基或C8-24-N,O,P,S-杂烷基;C6-12环烷基或C6-12- N,O,P,S-杂环烷基;C7-24烷芳基;C6-16芳基;C4-18-N,O,P,S-杂芳基;C6-16芳基或C4-18-N,O,P,S-杂芳基,其可被C1-12烷基、C5-8环烷基或C1-12烷氧基所单-或多-取代;
R2是C6-18烷基或C6-18-N,O,P,S-杂烷基;C5-12环烷基或C5-12- N,O,P,S-杂环烷基;C7-18烷芳基;C6-16芳基;C4-18-N,O,P,S-杂芳基;C6-16芳基或C4-18-N,O,P,S-杂芳基,其可被C1-12烷基;C6-8环烷基或C1-12烷氧基所单-或多-取代;
D是直链或支链的C1-24亚烷基或C1-24-N,O,P,S-亚烷基;C2-24烷叉基或C2-24-N,O,P,S-烷叉基;C5-8亚环烷基或C5-8-N,O,P,S-亚环烷基;未被取代或被直链或支链C1-18烷基,C5-8环烷基,C1-12烷氧基所单-或多-取代的C6-24亚芳基或C4-18-N,O,P,S-亚杂芳基;或-O-;-S-;
q是1至4;
r是4或5,当式(IV)中的P-R1基团是磷杂环的成分时,以由P引出的键中的*号表示;
Ra、Rb、Rd、Re、Rf、Rg及Rh各自独立的为氢;羟基;C1-12烷基;或未被取代或被C1-2烷基所单-、双-或三-取代的苯基;C7-9苯烷基;未被取代或被C1-2烷基所单-、双-或三-取代的C1-12烷氧基或C5-8环烷基;和Rc如前面Ra、Rb、Rd、Re、Rf、Rg及Rh的定义,或为式(VI)的基团,其中
Ra、Rb、Rd、Re、Rf、Rg及Rh如前面所定义,且Ri、Rj各自独立地为氢或C1-2烷基,其中Rd、Rc、Rf、Rg及Rh中至少有两个是氢;
X1是氢;C1-5烷基;氧自由基O*;-OH;-NO;-CH2CN;苄基;烯丙基;C1-10烷氧基;C5-6环烷氧基;C6-7芳氧基;C7-10芳烷氧基或其中芳基被C1-5烷基、卤原子或硝基取代的C7-10芳烷氧基;C3-6烯基;C3-6炔基;C1-5酰基;卤原子;未被取代或被C1-2烷基取代的苯基;
X2是氢; [CH2-CH2-C(O)-O-X5]基; [CH2-C(CH3)H-C(O)-O-X5 ]基;C1-10烷基;
X3及X4各自独立地是氢;未被取代或被C1-2烷基取代的苯基;或支链的C4-22烷基,且X3及X4中至少有一个为支链C4-10烷基;
X5是C10-16烷基。
特别优选的化合物中:
R1是C12-16烷基或C12-16-N,O,P,S-杂烷基;C6-8环烷基或C6-8- N,O,P,S-杂环烷基;C7-12烷芳基;C6-12芳基或C4-10-N,O,P,S-杂芳基;被C1-18烷基、C5-6环烷基或C1-8烷氧基所单-或多-取代的C6-12芳基或C4-10杂芳基;
R2是C8-18基或C8-18-N,O,P,S-杂烷基;C5-8环烷基或C5-8-N,O,P,S-杂环烷基;C7-12烷芳基;C6-12芳基;C4-10-N,O,P,S-杂芳基;被C1-8烷基,C5-6环烷基或C1-8烷氧基所单或多取代的C6-12芳基或C4-10-N,O,P,S-杂芳基;
D是直链或支链的C1-18亚烷基或C1-18-N,O,P,S-亚烷基;C2-18烷叉基或C22-18-N,O,P,S-烷叉基;C5-8亚环烷基或C5-8N,O,P,S-亚环烷基;未被取代或被直链或支链C1-12烷基,C5-8环烷基或C1-8烷氧基所单或多取代的C6-18亚芳基或C4-18-N,O,P,S-亚杂芳基;或-O-;-S-;
q是1至3;
r是4或5,当式(IV)中的P-R1基为磷杂环的成分时,以由P引出的键中的*号表示;
Ra、Rb、Rd、Re、Rf、Rg及Rh各自独立地是氢;羟基;C1-6烷基;或未被取代或被C1-2烷基所单-、双-或三-取代的苯基;C7-9苯烷基、C1-6烷氧基或C5-8环烷基,其是未被取代的或被C1-2烷基所单-、双-或三-取代;且Rc如前面Ra、Rb、Rd、Re、Rf、Rg及Rh的定义或为式(VI)的基团,其中
Ra、Rb、Rd、Re、Rf、Rg及Rh如前述的定义,Ri、Rj各自独立地是氢或C1-2烷基,且Rd、Re、Rf、Rg及Rh中至少有两个基是氢;
X1是氢;甲基;氧自由基O*;-OH;-NO;-CH2CN;苄基;烯丙基;C1-6烷氧基,C5-6环烷氧基;C6芳氧基;C3-6烯基;C3-6炔基;C1-5酰基;卤素;未被取代或被C1-2烷基取代的苯基;
X2是氢,[CH2-CH2-C(O)-O-X5]基,[CH2-C(CH3)H-C(O)-O-X5]基、C1-4烷基;
X3及X4各自独立地是氢,未被取代或被C1-2烷基取代的苯基,或支链的C4-6烷基,且X3及X4中至少有一基为支链C4-6烷基;且其中
X5是C12-14烷基。
特别优选的稳定剂组合物包含
a)三苯膦,
b)2-苯基苯并呋喃酮及
c)表氯醇和2,2,4,4-四甲基-7-氧杂-3,20-二氮杂-20-(2,3-环氧丙基)-二螺[5.1.11.2 ]-二十一烷-21-酮的聚合物,
其中成分a)对成分b)对成分c)的重量比为从1∶0.1∶1至1∶1∶3。
特别适合的为下列成分a)的代表例:
成分(A)
-三苯膦
-三(2-甲基苯基)膦
-三(4-甲基苯基)膦
-三(2-甲氧基苯基)膦
-三(4-甲氧基苯基)膦
-四环己基环四膦
-四叔丁基环四膦
-四联苯环四膦
-四苯环四膦
-五苯环五膦
-五联苯环五膦
-四苯二膦
-四环己基二膦
-联(二苯磷)甲烷
-1,2-双(二苯膦)乙烷
-1,3-双(二苯膦)丙烷
-1,4-双(二苯膦)丁烷
-1,5-双(二苯膦)戊烷
-1,6-双(二苯膦)己烷
-1,8-双(二苯膦)辛烷
-1,3-双(二苯膦)-2,2-二甲丙烷
-1,1,1-三(二苯膦甲基)甲烷
-1,1,1-三(二苯膦甲基)乙烷
-1,1,1-三(二苯膦甲基)丙烷
-1,1,1-三(二苯膦甲基)丁烷
-1,1,1-三(二苯膦甲基)-1-苯甲烷
-1,3-双(二苯膦甲基)-2,2-二苯膦丙烷
-1,3-双(二苯膦甲基)-2,2-二乙膦丙烷
-1,3-双(二苯膦)-2-甲基丙烷
空间位阻胺(成分C)的例子有:
-癸二酸双(2,2,6,6-四甲基-4-哌啶)酯
-琥珀酸双(2,2,6,6-四甲基-4-哌啶)酯
-癸二酯双(1,2,2,6,6-五甲基-4-哌啶)酯
-琥珀酸双(1,2,2,6,6-五甲基-4-哌啶)酯
-癸二酸双(1-辛氧-2,2,6,6-四甲基-4-哌啶)酯
-琥珀酸双(1-辛氧-2,2,6,6-四甲基-4-哌啶)酯
-丙二酸双(1,2,2,6,6-五甲基-4-哌啶)正丁基-3,5-双叔丁基-4-羟苄酯
-丙二酸双(1,2,2,6,6-五甲基哌啶)-2-正丁基-2-(2-羟-3,5-双叔丁苄基)酯
-次氮基三醋酸(2,2,6,6-四甲基-4-哌啶)酯
-1,2,3,4-丁烷四羧酸四(2,2,6,6-四甲基-4-哌啶)酯
-4-苯甲酰-2,2,6,6-四甲基哌啶
-4-硬脂酰氧-2,2,6,6-四甲基哌啶
-4-十六烷氧-2,2,6,6-四甲基哌啶和4-硬脂酰氧-2,2,6,6-四甲基哌啶的混合物
-1,5-二噁螺[5.5]十一烷-3,3-双羧酸双(2,2,6,6-四甲基-4-哌啶)酯
-1,5-二噁螺[5.5]十一烷-3,3-双羧酸双(1,2,2,6,6-五甲基-4-哌啶)酯
-3-正辛基-7,7,9,9-四甲基-1,3,8-三氮杂螺[4.5]癸-2,4-二酮
-8-乙酰-3-十二烷基-7,7,9,9-四甲基-1,3,8-三氮杂螺[4.5]癸-2,4-二酮
-3-十二烷基-1-(2,2,6,6-四甲基-4-哌啶)吡咯烷-2,5-二酮
-(N-(2,2,6,6-四甲基-4-哌啶)-正十二烷基琥珀酰亚胺)
-3-十二烷基-1-(1,2,2,6,6-五甲基-4-哌啶)吡咯烷-2,5-二酮
-(N-(1,2,2,6,6-五甲基-4-哌啶)-正-十二烷基琥珀酰亚胺)
-3-十二烷基-1-(1-乙酰-2,2,6,6-四甲基-4-哌啶)吡咯烷-2,5-二酮
-(N-(1-乙酰-2,2,6,6-四甲基-4-哌啶)-正-十二烷基琥珀酰亚胺)
-1,1’-(1,2-乙二基)-双(3,3,5,5-四甲基哌嗪酮)
-1-(2-羟乙基)-2,2,6,6-四甲基-4-羟哌啶和琥珀酸或琥珀酸二烷酯的缩合产物
-N,N’-双(2,2,6,6-四甲基-4-哌啶)六亚甲基二胺和4-叔辛氨基-2,6-二氯-1,3,5-三嗪的缩合产物
-N,N’-双(2,2,6,6-四甲基-4-哌啶)六亚甲基二胺和4-环己氨基-2,6-二氯-
1,3,5-三嗪的缩合产物
-N,N’-双(2,2,6,6-四甲基-4-哌啶)六亚甲基二胺和4-吗啉代-2,6-二氯-1,3,5-三嗪的缩合产物
-2-氯-4,6-双(4-正丁氨基-2,2,6,6-四甲基哌啶)-1,3,5-三嗪和1,2-双(3-氨基丙基氨基)乙烷的缩合产物
-2-氯-4,6-双(4-正丁氨基-1,2,2,6,6-五甲基哌啶)-1,3,5-三嗪和1,2-双(3-氨基丙基氨基)乙烷的缩合产物
-2-氯-4,6-双(4-正丁氨基-1,2,2,6,6-五甲基哌啶)-1,3,5-三嗪和1,6,11-三氨基十一烷的缩合产物
-1,2-双(3-氨基丙基氨基)乙烷和2,4,6-三氯-1,3,5-三嗪和4-丁氨基-2,2,6,6-四甲基哌啶的反应产物
-表氯醇和2,2,4,4-四甲基-7-氧杂-3,20-二氮杂-20-(2,3-环氧丙基)二螺[5.1.11.12]-二十一烷-21-酮的聚合物
特别合适的是可由一或多个成分a)至c)相结合而组成的所有混合物。
和含有除其它稳定剂以外的空间位阻酚类衍生物的系统的现有技术比较起来,在聚烯烃制品(尤其是聚烯烃纤维)中采用本新系统可在加工及使用寿命中避免因形成醌型产物和受NOx气的作用(气褪色)而造成的褪色。
和传统含酚制剂(见下面的实施例)比较起来,本发明的另一优点是稳定剂的总浓度较低。
稳定剂组合物的浓度是占所要稳定化的聚合物重量的0.001至5%,优选为0.01至1%,更优选为0.1至0.5%。
聚合物可含有其他成分,如氨基酸类加工稳定剂,有机及无机紫外线吸收剂,除酸剂,金属钝化剂,成核剂,填料,抗静电剂,颜色改良剂,助塑剂,润滑剂,金属钝化剂,染料,颜料,乳化剂,阻燃剂,发泡剂,交联剂,抗粘连剂,增滑剂,硫系增效剂,无机载体(如SiO2)及加工助剂。
依本发明可被稳定化的合适热塑性聚合物例如有:
1.单烯烃及二烯烃聚合物,如聚丙烯(PP),聚异丁烯,聚丁-1-烯,聚-4-甲基戊-1-烯,聚异戊二烯或聚丁二烯,以及环烯烃(如环戊烯及降冰片烯)的聚合物;还有可任选地交联的聚乙烯(PE),如高密度聚乙烯(HDPE),高分子量高密度聚乙烯(HMW-HDPE),超高分子量高密度聚乙烯(UHMW-HDPE),中密度聚乙烯(HMDPE),低密度聚乙烯(LDPE),线性低密度聚乙烯(LLDPE),支链低密度聚乙烯(BLDPE)。
聚烯烃,即前面列举的单烯烃的聚合物,特别是聚乙烯及聚丙烯,可用各种方法,尤其是下法制备:
a)自由基聚合反应(通常是在高压及升温下)
b)通常是含有一或多种周期表IVb,Vb,VIb或VIII金属的催化剂的催化聚合反应。这些金属通常具有一或多种配合体,如氧化物,卤化物,醇化物,酯,醚,胺,烷基,烯基及/或芳基,其可π-或σ-配位。这些金属配合物可呈自由态或固定在基材上,如负载于活化氯化镁,氯化钛(III),氧化铝或二氧化硅上。这些催化剂可溶于或不溶于聚合介质中。这些催化剂可直接呈活性用于聚合中,或进一步使用活化剂,如烷基金属,氢化金属,烷基卤化金属,烷基氧化金属或金属烷基环氧化物,其中金属为周期表Ia,IIa及/或IIIa的元素。活化剂可例如用其他的酯、醚、胺或甲硅烷醚基改性。这些催化剂通常称为菲利浦、印地安那标准石油、齐格勒(纳塔)、TNZ(杜邦)、金属茂或单位点催化剂(SSC)。
2.前述1)聚合物的混合物,如聚丙烯/聚异丁烯,聚乙烯/聚异丁烯,聚丙烯/聚乙烯(如PP/HDPE/LDPE),以及不同类型聚乙烯互相的混合物(如LDPE/HDPE)。
3.单烯烃和二烯烃互相的共聚物,或与其他乙烯基单体的共聚物,如乙烯-丙烯共聚物,线型低密度聚乙烯(LLDPE)及其和低密度聚乙烯(LDPE)的混合物,丙烯/1-丁烯共聚物,丙烯/异丁烯共聚物,乙烯/1-丁烯共聚物,乙烯/己烯共聚物,乙烯/甲基戊烯共聚物,乙烯/庚烯共聚物,乙烯/辛烯共聚物,丙烯/丁二烯共聚物,异丁烯/异戊二烯共聚物,乙烯/丙烯酸烷酯共聚物,乙烯/甲基丙烯酸烷酯共聚物,乙烯/醋酸乙烯酯共聚物及其与一氧化碳的共聚物,或乙烯/丙烯酸共聚物及其盐(离聚物),以及乙烯,丙烯和二烯(如己二烯、二环戊二烯或乙叉-降冰片烯)的三元共聚物;这些共聚物互相及和1)所述聚合物的混合物,如聚丙烯/乙烯/丙烯共聚物,LDPE/乙烯/醋酸乙烯酯共聚物,LDPE/乙烯/丙烯酸共聚物,LLDPE/乙烯/醋酸乙烯酯共聚物,LLDPE/乙烯/丙烯酸共聚物,以及交替或无规聚亚烷基一氧化碳共聚物及其和其他聚合物(如聚酰胺)的混合物。
4.烃树脂(如C5-9),包含其氢化改性物(如增粘树脂)以及聚亚烷基和淀粉的混合物。
5.聚苯乙烯,聚(对-甲基苯乙烯),聚(α-甲基苯乙烯)。
6.苯乙烯或α-甲基苯乙烯和二烯或丙烯酸衍生物的共聚物,如苯乙烯/丁二烯,苯乙烯/丙烯腈,苯乙烯/甲基丙烯酸烷酯,苯乙烯/丁二烯/丙烯酸烷酯,苯乙烯/丁二烯/甲基丙烯酸烷酯,苯乙烯/马来酸酐,苯乙烯/丙烯腈/甲基丙烯酸酯共聚物;高冲击强度苯乙烯共聚物和其他聚合物(如聚丙烯酸酯,二烯聚合物或乙烯/丙烯/二烯三元共聚物)的混合物;苯乙烯的嵌段共聚物,如苯乙烯/丁二烯/苯乙烯,苯乙烯/异戊二烯/苯乙烯,苯乙烯/乙烯-丁烯/苯乙烯或苯乙烯/乙烯-丙烯/苯乙烯嵌段共聚物。
7.苯乙烯,或α-甲基苯乙烯的接枝共聚物,如苯乙烯接枝在聚丁二烯,苯乙烯接枝在聚丁二烯-苯乙烯或聚丁二烯-丙烯腈共聚物,苯乙烯及丙烯腈(或甲基丙烯腈)接枝在聚丁二烯,苯乙烯,丙烯腈及甲基丙烯酸甲酯接枝在聚丁二烯,苯乙烯,马来酸酐接枝在聚丁二烯,苯乙烯,丙烯腈及马来酸酐或马来酰亚胺接枝在聚丁二烯,苯乙烯及马来酰亚胺接枝在聚丁二烯,苯乙烯及丙烯酸烷酯或甲基丙烯酸烷酯接枝在聚丁二烯,苯乙烯及丙烯腈接枝在乙烯-丙烯-二烯三元共聚物,苯乙烯及丙烯腈接枝在聚丙烯酸烷酯或聚甲基丙烯酸烷酯,苯乙烯及丙烯腈接枝在丙烯酸酯-丁二烯共聚物,以及其和6)中所述共聚物的混合物,例如共聚物混合物已知有ABS,MBS,ASA或AES聚合物。
8.含卤聚合物,如聚氯丁二烯,氯化橡胶,异丁烯-异戊二烯共聚物的氯化及溴化物(卤丁基橡胶),氯化或磺氯化聚乙烯,乙烯及氯化乙烯共聚物,表氯醇均及共聚物,尤其是含卤的乙烯基化合物的聚合物,如聚氯乙烯,聚偏二氯乙烯,聚氟乙烯,聚偏二氟乙烯;以及其共聚物,如氯乙烯/偏二氯乙烯,氯乙烯/醋酸乙烯酯或偏二氯乙烯/醋酸乙烯酯共聚物。
9.衍生自α,β-不饱和酸及其衍生物的聚合物,如聚丙烯酸酯及聚甲基丙烯酸酯,聚丙烯腈,聚丙烯酰胺及以丙烯酸丁酯冲击改性的聚甲基丙烯酸甲酯。
10.前面9)所述单体互相的共聚物或和其他不饱和单体的共聚物,如丙烯腈/丁二烯共聚物,丙烯腈/丙烯酸烷酯共聚物,丙烯腈/丙烯酸烷氧基烷酯共聚物,丙烯腈/卤化乙烯共聚物或丙烯腈/甲基丙烯酸烷酯/丁二烯三元共聚物。
11.由不饱和醇及胺或其酰衍生物或缩醛所衍生的聚合物,如聚乙烯醇,聚醋酸乙烯酯,聚硬脂酸乙烯酯,聚苯甲酸乙烯酯,聚马来酸乙烯酯,聚丁缩醛乙烯酯,聚苯二甲酸烯丙酯或聚烯丙基蜜胺;及其和前面1)所述的烯烃的共聚物。
12.环醚的均聚物及共聚物,如聚亚烷基二醇,聚环氧乙烷,聚环氧丙烷或其和双缩水甘油醚的共聚物。
13.聚缩醛,如聚甲醛及含有共聚单体(如环氧乙烷)的聚甲醛;以热塑性聚氨基甲酸酯、丙烯酸酯或MBS改性的聚缩醛。
14.聚苯醚及聚苯硫醚,以及其和苯乙烯聚合物或聚酰胺的混合物。
15.一方面衍生自具羟基末端的聚醚、聚酯及聚丁二烯,而另一方面衍生自脂族或芳族聚异氰酸酯以及其前体的聚氨基甲酸酯。
16.衍生自二胺及二羧酸和/或氨基羧酸或对应的内酰胺的聚酰胺及共聚酰胺,如聚酰胺4,6,6/6,6/10,6/9,6/12,4/6,12/12,11及12,由间-二甲苯、二胺及己二酸所衍生的芳族聚酰胺;由六亚甲基二胺和间苯二甲酸和/或对苯二甲酸为原料,且使用或不用弹性体为改性剂的聚酰胺,如聚-2,4,4-三甲基六亚甲基对苯二甲酰胺或聚间亚苯基间苯二甲酰胺。前述聚酰胺和聚烯烃、烯烃共聚物、离聚物或化学键结或接枝的弹性体的嵌段共聚物;或和聚醚,如聚乙二醇,聚丙二醇,或聚四亚甲基二醇的嵌段共聚物,以及用EPDM或ABS改性的聚酰胺或共聚酰胺;及在加工时缩合的聚酰胺(RIM聚酰胺系统)。
17.聚脲,聚酰亚胺,聚酰胺-酰亚胺,聚醚酰亚胺,聚酯酰胺,聚乙内酰脲及聚苯并咪唑。
18.衍生自二羧酸及二醇和/或羟羧酸或对应的内酯的聚酯,如聚对苯二甲酸乙二酯,聚对苯二甲酸丁二酯,聚1,4-二羟甲基环己烷对苯二甲酸酯,聚羟苯甲酸酯,以及衍生自具羟基末端聚醚的嵌段聚醚酯;以及用聚碳酸酯或MBS改性的聚酯。
19.聚碳酸酯及聚酯碳酸酯。
20.聚砜,聚醚砜及聚醚酮。
21.一方面衍生自醛,另方面衍生自酚、脲或蜜胺的交联聚合物,如酚/甲醛树脂,脲/甲醛树脂及蜜胺/甲醛树脂。
22.干性及非干性醇酸树脂。
23.衍生自饱和及不饱和二羧酸和多羟醇的共聚酯的不饱和聚酯树脂,其以乙烯基化合物为交联剂,以及其低燃性的含卤改性物。
24.衍生自被取代的丙烯酸酯(如环氧丙烯酸酯,氨基甲酸酯丙烯酸酯或聚酯丙烯酸酯)的可交联丙烯酸树脂。
25.醇酸树脂,聚酯树脂,及与蜜胺树脂、脲树脂、异氰酸酯、异氰脲酸酯、聚异氰酸酯或环氧树脂交联的丙烯酸酸树脂。
26.衍生自脂族、环脂族、杂环或芳族缩水甘油基化合物的交联环氧树脂,如双酚A二缩水甘油醚,双酚F二缩水甘油醚的产物,其利用通常的硬化剂,如酐或胺进行交联,并且使用或不用促进剂。
27.天然聚合物,如纤维素,天然橡胶,明胶及其以聚合物同系物的方式做化学改性的衍生物,如醋酸纤维素,丙酸纤维素及丁酸纤维素,或例如甲基纤维素的纤维素醚;以及松香及其衍生物。
28.前述聚合物的混合物(聚掺混物),如PP/EPDM,聚酰胺/EPDM或ABS,PVC/EVA,PVC/ABS,PVC/MBS,PC/ABS,PBTP/ABS,PC/ASA,PC/PBT,PVC/CPE,PVC/丙烯酸酯,POM/热塑性PUR,PC/热塑性PUR,POM/丙烯酸酯,POM/MBS,PPO/MBS,PPO/HIPS,PPO/PA6,6及PA/HDPE,PA/PP,PA/PPO,PBT/ABS或PBT/PET/PC的共聚物。
29.构成纯单体化合物或其混合物的天然或合成有机物质,如矿物油、动物或植物脂、油、蜡,或基于合成酯(如苯二甲酸酯,己二酸酯,磷酸酯或偏苯三酸酯)的油、蜡和脂,以及合成酯和矿物油按照任何所希望的重量比例的混合物,其被用作例如纺丝精整剂,及其水性乳液。
30.天然或合成像胶的水性乳液,如天然橡胶胶乳或羧基化苯乙烯-丁二烯共聚物胶乳。
本发明的稳定剂组合物或欲稳定化的热塑性聚合物必要时还可含有其他添加剂,如抗氧化剂,光稳定剂,金属钝化剂,抗静电剂,阻燃剂,润滑剂,成核剂,除酸剂(碱性辅稳定剂),颜料及填料。可另外配合使用的其他合适添加剂如列于下面的化合物:
1.抗氧化剂
1.1烷基化单酚,如2,6-双叔丁基-4-甲酚,2-丁基-4,6-二甲酚,2,6-双叔丁基-4-乙酚,2,6-双叔丁基-4-正丁酚,2,6-双叔丁基-4-异丁酚,2,6-二环戊基-4-甲酚,2-(α-甲基环己基)-4,6-二甲酚,2,6-双十八烷基-4-甲酚,2,4,6-三环己酚,2,6-双叔丁基-4-甲氧甲酚,直链或有支链的壬酚,如2,6-双壬基-4-甲酚,2,4-二甲基-6-(1-甲基十一烷-1’-基)酚,2,4-二甲基-6-(1’-甲基十七烷-1’-基)酚,2,4-二甲基-6-(1’-甲基十三烷-1’-基)酚及其混合物。
1.2烷硫甲酚,如2,4-二辛硫甲基-6-叔丁酚,2,4-二辛硫甲基-6-甲酚,2,4-二辛硫甲基-6-乙酚,2,6-双十二烷硫甲基-4-壬酚,
1.3氢醌及烷基化氢醌,如2,6-双叔丁基-4-甲氧酚,2,5-双叔丁基氢醌,2,5-双叔戊基氢醌,2,6-二苯-4-十八烷氧酚,2,6-双叔丁氢醌,2,5-双叔丁基-4-羟苯甲醚,3,5-双叔丁基-4-羟苯甲醚,硬脂酸3,5-双叔丁基-4-羟苯酯,己二酸双(3,5-双叔丁基-4-羟苯)酯。
1.4羟基化硫二苯醚,如2,2’-硫双(6-叔丁基-4-甲酚),2,2’-硫双(4-辛酚),4,4’-硫双(6-叔丁基-3-甲酚),4,4’-硫双(6-叔丁基-2-甲酚),4,4’-硫双(3,6-二仲戊酚),4,4’-双(2,6-二甲基-4-羟苯)二硫化物。
1.5烷叉基双酚,如2,2’-亚甲基双(6-叔丁基-4-甲酚),2,2’-亚甲基双(6-叔丁基-4-乙酚),2,2’-亚甲基双[4-甲基-6-(α-甲基环己基)酚],2,2’-亚甲基双(4-甲基-6-环己酚),2,2’-亚甲基双(6-壬基-4-甲酚),2,2’亚甲基双(4,6-双叔丁酚),2,2’-乙叉双(4,6-双叔丁酚),2,2’-乙叉双(6-叔丁基-4-异丁酚),2,2’-亚甲基双[6-(α-甲苄)-4-壬酚],2,2’-亚甲基双[6-(α,α-二甲苄)-4-壬酚],4,4’-亚甲基双(2,6-双叔丁酚),4,4’-亚甲基双(6-叔丁基-2-甲酚),1,1-双(5-叔丁基-4-羟-2-甲苯)丁烷,2,6-双(3-叔丁基-5-甲基-2-羟苯)-4-甲酚,1,1,3-三(5-叔丁基-4-羟-2-甲苯)丁烷,1,1-双(5-叔丁基-4-羟-2-甲苯)-3-正十二烷基巯丁烷,双(3-叔丁基-4-羟-5-甲苯)双环戊二烯,对苯二甲酸双[2-(3’-叔丁基-2’-羟-5’-甲苄)-6-叔丁基-4-甲苯[酯,1,1’-双(3,5-二甲基-2-羟苯)丁烷,2,2-双(3,5-双叔丁基-4-羟苯)丙烷,2,2-双(5-叔丁基-4-羟-2-甲苯)-4-正十二烷基巯丁烷,1,1,5,5-四(5-叔丁基-4-羟-2-甲苯)戊烷,乙二醇双[3,3-双(3’-叔丁基-4’-羟苯)丁酸酯]。
1.6 O-,N-及S-苄基化合物,如3,5,3’,5’-四叔丁基-4,4’-双羟二苄醚,4-羟-3,5-双甲基苄基巯乙酸十八烷酯,三(3,5-双叔丁基-4-羟苄)胺,双硫对苯二甲酸双(4-叔丁基-3-羟-2,6-双甲苄)酯,双(3,5-双叔丁基-4-羟苯)硫,3,5-双叔丁基-4-羟苄巯醋酸异辛酯,4-羟-3,5-双叔丁苄巯醋酸十三烷酯。
1.7羟苄基化丙二酸酯,如2,2-双(3,5-双叔丁基-2-羟苄)丙二酸双十八烷酯,2-(3-叔丁基-4-羟-5-甲苄)丙二酸双十八烷酯,巯乙基-2,2-双(3,5-双叔丁基-4-羟苄)丙二酸双十二烷酯,2,2-双(3,5-双叔丁基-4-羟苄)丙二酸双[4-(1,1,3,3-四甲丁基)苯]酯。
1.8芳族羟苄基化合物,如1,3,5-三(3,5-双叔丁基-4-羟苄)-2,4,6-三甲苯,1,4-双(3,5-双叔丁基-4-羟苄)-2,3,5,6-四甲基苯,2,4,6-三(3,5-双叔丁基-4-羟苯)酚。
1.9三嗪化合物,如2,4-双辛巯-6-(3,5-双叔丁基-4-羟苯氨基)-1,3,5-三嗪,2-辛巯-4,6-双(3,5-双叔丁基-4-羟苯氨基)-1,3,5-三嗪,2-辛巯-4,6-双(3,5-双叔丁基-4-羟苯氧)-1,3,5-三嗪,2,4,6-三(3,5-双叔丁基-4-羟苯氧)-1,2,3-三嗪,异氰脲酸1,3,5-三(3,5-双叔丁基-4-羟苄)酯,异氰脲酸1,3,5-三(4-叔丁基-3-羟-2,6-二甲苄)酯,2,4,6-三(3,5-双叔丁基-4-羟苯乙基)-1,3,5-三嗪,1,3,5-三(3,5-双叔丁基-4-羟苯丙酰)六氢-1,3,5-三嗪,异氰脲酸1,3,5-三(3,5-双环己基-4-羟苯)酯。
1.10苄基膦酸酯,如2,5-双叔丁基-4-羟苄基膦酸二甲酯,3,5-双叔丁基-4-羟苄-4-羟苄膦酸二乙酯,3,5-双叔丁基-4-羟苄膦酸双十八烷酯,5-叔丁基-4-羟-3-甲苄膦酸双十八烷酯,3,5-双叔丁基-4-羟苄膦酸单乙酯的钙盐。
1.11酰氨基酚,如4-羟月桂酰替苯胺,4-羟硬脂酰替苯胺,N-(3,5-双叔丁基-4-羟苯)氨基甲酸辛酯。
1.12β-(3,5-双叔丁基-4-羟苯)丙酸和下列单-或多-羟醇所形成的酯:例如甲醇,乙醇,正辛醇,异辛醇,十八烷醇,1,6-己二醇,1,9-壬二醇,乙二醇,1,2-丙二醇,新戊二醇,硫二甘醇,二甘醇,三甘醇,季戊四醇,异氰脲酸三(羟乙基)酯,N,N’-双(羟乙基)草酰胺,3-噻-十一烷醇,3-噻-十五烷醇,三甲基己二醇,三羟甲基丙烷,4-羟甲基-1-磷-2,6,7-三噁双环[2.2.2]辛烷。
1.13β-(5-叔丁基-4-羟-3-甲苯)丙酸和下列单-或多-羟醇所形成的酯,例如甲醇,乙醇,正丁醇,异辛醇,十八烷醇,1,6-己二醇,1,9-壬二醇,乙二醇,1,2-丙二醇,新戊二醇,硫二甘醇,二甘醇,三甘醇,季戊四醇,异氰脲酸三(羟乙基)酯,N,N’-双(羟乙基)草酰胺,3-噻-十一烷醇,3-噻-十五烷醇,三甲基己二醇,三羟甲基丙烷,4-羟甲基-1-磷-2,6,7-三噁双环[2.2.2]辛烷。
1.14 β-(3,5-二环己基-4-羟苯)丙酸和下列单-或多-羟醇所形成的酯:例如甲醇,乙醇,正辛醇,异辛醇,十八烷醇,1,6-己二醇,1,9-壬二醇,乙二醇,1,2-丙二醇,新戊二醇,硫二甘醇,二甘醇,三甘醇,季戊四醇,异氰脲酸三(羟乙基)酯,N,N’-双(羟乙基)草酰胺,3-噻-十一烷醇,3-噻-十五烷醇,三甲基己二醇,三羟甲基丙烷,4-羟甲基-1-磷-2,6,7-三噁双环[2.2.2]辛烷。
1.15 3,5-双叔丁基-4-羟苯醋酸和下列单-或多-羟醇所形成的酯:例如甲醇,乙醇,正辛醇,异辛醇,十八烷醇,1,6-己二醇,1,9-壬二醇,乙二醇,1,2-丙二醇,新戊二醇,硫二甘醇,二甘醇,三甘醇,季戊四醇,异氰脲酸三(羟乙基)酯,N,N’-双(羟乙基)草酰胺,3-噻-十一烷醇,3-噻-十五烷醇,三甲基己二醇,三羟甲基丙烷,4-羟甲基-1-磷-2,6,7-三噁双环[2.2.2]辛烷。
1.16 3,3-双(3’-叔丁基-4’-羟苯)丁酸和下列单-或多-羟醇所形成的酯:例如甲醇,乙醇,正辛醇,异辛醇,十八烷醇,1,6-己二醇,1,9-壬二醇,乙二醇,1,2-丙二醇,新戊二醇,硫二甘醇,二甘醇,三甘醇,季戊四醇,异氰脲酸三(羟乙基)酯,N,N’-双(羟乙基)草酰胺,3-噻-十一烷醇,3-噻-十五烷醇,三甲基己二醇,三羟甲基丙烷,4-羟甲基-1-磷2,6,7-三噁双环[2.2.2]辛烷。
1.17β-(3,5-双叔丁基-4-羟苯)丙酸的酰胺,如N,N’-双(3,5-双叔丁基-4-羟苯丙酰)六亚甲基二胺,N,N’-双(3,5-双叔丁基-4-羟苯丙酰)三亚甲基二胺,N,N’-双(3,5-双叔丁基-4-羟苯丙酰)肼。
1.18生育酚,如α-生育酚,β-生育酚,γ-生育酚,σ-生育酚及其混合物(维生素E)。
1.19抗坏血酸(维生素C)。
1.20胺抗氧化剂,如N,N’-二异丙基-对-苯二胺,N,N’-双仲丁基-对-苯二胺,N,N’-双(1,4-二甲戊基)-对-苯二胺,N,N’-双(1-乙基-3-甲苯)-对-苯二胺,N,N’-双(1-甲庚基)-对-苯二胺,N,N’-二环己基-对-苯二胺,N,N’-二苯基-对-苯二胺,N,N’-双(萘-2-)-对-苯二胺,N-异丙基-N’-苯基-对-苯二胺,N-(1,3-二甲丁基)-N’-苯基-对苯二胺,N[(1-甲庚基)-N’-苯基-对苯二胺,N-环己基-N’-苯基-对苯二胺,4-(甲苯磺氨基)二苯胺,N,N’-双甲基-N,N’-双仲丁基-对-苯二胺,二苯胺,N-丙烯二苯胺,4-异丙氧二苯胺,N-苯基-1-萘胺,N-(4-叔辛苯)-1-萘胺,N-苯-2-萘胺,辛基化二苯胺,例如对,对’-双叔辛基二苯胺,4-正丁氨基酚,4-丁酰氨基酚,4-壬酰氨基酚,4-十二烷酰氨基酚,4-十八烷酰氨基酚,双(4-甲氧苯)胺,2,6-双叔丁基-4-二甲基氨基甲酚,2,4’-二氨基二苯甲烷,4,4’-二氨基二苯甲烷,N,N,N’,N’,-四甲基-4,4’-二氨基二苯甲烷,1,2-双[(2-甲苯)氨基]乙烷,1,2-双(苯氨基)丙烷,(邻甲苯)双胍,双[4-(1’,3’-二甲丁基)苯基]胺,叔辛基化N-苯-1-萘胺,单-及双-烷基化叔丁基/叔辛基二苯胺的混合物,单-及双-烷基化壬二苯胺的混合物,单-及双-烷基化十二烷二苯胺的混合物,单-及双-烷基化异丙基/异己基二苯胺的混合物,单-及双-烷基化叔丁基二苯胺的混合物,2,3-二氢-3,3-二甲基-4H-1,4-苯并三嗪,吩噻嗪,单-及双-烷基化叔丁基/叔辛基吩噻嗪的混合物,单-及双-烷基化叔辛基吩噻嗪的混合物,N-丙烯吩噻嗪,N,N,N’,N’-四苯-1,4-二氨基丁-2-烯,N,N-双(2,2,6,6-四甲基哌啶-4-基)六亚甲基二胺,癸二酸双(2,2,6,6-四甲基哌啶-4-基)酯,2,2,6,6-四甲基哌啶-4-酮,2,2,6,6-四甲基哌啶-4-醇。
2.紫外吸收剂及光稳定剂
2.12-(2’-羟基苯基)苯并三唑,如2-(2’-羟基-5’-甲苯基)苯并三唑,2-(3’,5’-双叔丁基-2’-羟苯基)苯并三唑,2-(5’-叔丁基-2’-羟苯)苯并三唑,2-[2’-羟-5’-(1,1,3,3-四甲丁基)苯基]苯并三唑,2-(3’,5’-双叔丁基-2’-羟-苯基)-5-氯苯并三唑,2-(3’-叔丁基-2’-羟基-5’-甲基苯基)-5-氯苯并三唑,2-(3’-仲丁基-5’-叔丁基-2’-羟苯)苯并三唑,2-(2’-羟-4’-辛氧苯基)苯并三唑,2-(3’-5’-双叔戊基-2’-羟苯)苯并三唑,2-(3’,5’-双(α,α-二甲苄)-2’-羟苯)苯并三唑,2-(3’-叔丁基-2’-羟-5’-(2-辛氧羰乙基)苯基)-5-氯苯并三唑,2-(3’-叔丁基-5’-[ 2-(2-乙基己氧基)羰乙基]-2’-羟苯)-5-氯苯并三唑,2-(3’-叔丁基-2’-羟-5’-(2-甲氧羰乙基)苯)-5-氯苯并三唑,2-(3’-叔丁基-2’-羟-5’-(2-甲氧羰乙基)苯基)苯并三唑,2-(3’-叔丁基-2’-羟-5’-(2-辛氧羰乙基)苯基)苯并三唑,2-(3’-叔丁基-5’-[2-(2-乙基己氧基)羰乙基]-2’-羟苯)苯并三唑,2-(3’-十二烷-2’-羟基-5’-甲基苯基)苯并三唑及2-(3’-叔丁基-2’-羟基-5’-(2-异辛氧羰乙基)苯基苯并三唑的混合物,2,2’-亚甲基双[4-(1,1,3,3-四甲丁基)-6-苯并三唑-2-基酚],2-(3’-叔丁基-5’-(2-甲氧羰乙基)-2’-羟苯)苯并三唑与聚乙二醇300的酯基转移产物;[[R-CH2CH2-COO-(CH2)3]2,式中R=2’-叔丁基-4’-羟-5’-2H苯并三唑-2-基苯。
2.2 2-羟二苯甲酮,如4-羟基,4-甲氧基,4-辛氧基,4-癸氧基,4-十二烷氧基,4-苄氧基,4,2’,4’-三羟基及2’-羟基-4,4’-双甲氧基的衍生物。
2.3被取代或未被取代的苯甲酸的酯,如水杨酸4-叔丁苯酯,水杨酸苯酯,水杨酸辛苯酯,二苯甲酰间苯二酚,双(4-叔丁苯酰)间苯二酚,苯甲酰间苯二酚,3,5-双叔丁基-4-羟苯甲酸2,4-双叔丁苯酯,3,5-双叔丁基-4-羟苯甲酸十六烷酯,3,5-双叔丁基-4-羟苯甲酸十八烷酯,3,5-双叔丁基-4-羟苯甲酸2-甲基-4,6-双叔丁苯酯。
2.4丙烯酸酯,如α-氰-β,β-二苯丙烯酸乙酯或α-氰-β,β-二苯丙烯酸异辛酯,α-羰甲氧肉桂酸甲酯,α-氰-β-甲基-对-甲氧肉桂酸甲酯或α-氰-β-对-甲氧肉桂酸丁酯,α-羰甲氧-对-甲氧肉桂酸甲酯及N-(β-羰甲氧-β-氰乙烯)-2-甲基二氢吲哚。
2.5镍化合物,如2,2’-硫双[4-(1,1,3,3-四甲丁基)酚]的镍配合物,如1∶1或1∶2配合物,有或无额外的配合体,如正丁胺,三乙醇胺或N-环己二乙醇胺,二丁基二硫代氨基甲酸镍,单烷酯的镍盐,如4-羟-3,5-双叔丁苯膦酸的甲酯或乙酯的镍盐,酮肟如2-羟基-4-甲基苯基十一烷酮肟的镍配合物,1-苯基-4-月桂酰-5-羟基吡唑(有或无其他配合体)的镍配合物。
2.6空间位阻胺,如癸二酸双(2,2,6,6-四甲基哌啶-4-基)酯,戊二酸双(2,2,6,6-四甲基哌啶-4-基)酯,琥珀酸双(2,2,6,6-四甲基哌啶-4-基)酯,癸二酸双(1,2,2,6,6-五甲基哌啶-4-基)酯,戊二酸双(1,2,2,6,6-五甲基哌啶-4-基)酯,山萮酸2,2,6,6-四甲基哌啶酯,山萮酸1,2,2,6,6-五甲基哌啶酯,1-羟乙基-2,2,6,6-四甲基-4-羟哌啶和琥珀酸的缩合物,N,N’-双(2,2,6,6-四甲基-4-哌啶)六亚甲基二胺和4-叔辛氨基-2,6-二氯-1,3,5-均-三嗪的缩合物,次氮基醋酸三(2,2,6,6-四甲基-4-哌啶)酯,1,2,3,4-丁四酸四(2,2,6,6-四甲基-4-哌啶)酯,1,1’-(1,2-乙二基)双(3,3,5,5-四甲基哌嗪酮),4-苯甲酰2,2,6,6-四甲基哌啶,4-硬脂酰氧-2,2,6,6-四甲基哌啶,4-硬脂酰氧-2,2,6,6-四甲基哌啶,4-硬脂酰氧-1,2,2,6,6-五甲基哌啶,4-硬脂酰氧-1,2,2,6,6-五甲基哌啶,2-正丁基-2-(2-羟-3,5-双叔丁苄)丙二酸双(1,2,2,6,6-五甲基哌啶)酯,2-正丁基-2-(4-羟-3,5-双叔丁苄)丙二酸双(1,2,2,6,6-五甲基哌啶)酯,3-正辛基-7,7,9,9-四甲基-1,3,8-三氮杂螺[4.5]癸-2,4-二酮,癸二酸双(1-辛氧-2,2,6,6-四甲基哌啶)酯,琥珀酸双(1-辛氧-2,2,6,6-四甲基哌啶)酯,N,N’-双(2,2,6,6-四甲基-4-哌啶)六亚甲基二胺和4-吗啉代-2,6-二氯-1,3,5-三嗪的缩合物,N,N’-双(2,2,6,6-四甲基-4-哌啶)六亚甲基二胺和4-环己氨基-2,6-二氯-1,3,5-三嗪的缩合物,2-氯-4,6-双(4-正丁氨基-2,2,6,6-四甲基哌啶)-1,3,5-三嗪和1,2-双(3-氨基丙基氨基)乙烷的缩合物,2-氯-4,6-双(4-甲氧丙氨基-2,2,6,6-四甲基哌啶)-1,3,5-三嗪和1,2-双(3-氨基丙基氨基)乙烷的缩合物,2-氯-4,6-双(4-甲氧丙氨基-1,2,2,6,6-五甲基哌啶)-1,3,5-三嗪和1,2-双(3-氨基丙基氨基)乙烷的缩合物,2-氯-4,6-双(4-正丁氨基-1,2,2,6,6-五甲基哌啶)-1,3,5-三嗪和1,2-双(3-氨基丙基氨基)乙烷的缩合物,2-氯-4,6-双(4-正丁氨基-2,2,6,6-四甲基哌啶)-1,3,5-三嗪和单-或多-官能胺(其中在胺上的一个至全部的活性氢原子被置换),如亚乙基二胺,二亚乙基三胺,三亚乙基四胺,六亚甲基二胺,1,2-双(3-氨基丙基氨基)乙烷的反应产物,2-氯-4,6-双(4-正丁氨基-1,2,2,6,6-五甲基哌啶)-1,3,5-三嗪和单-或多-官能胺(其中胺上有一个至全部活性氢原子被置换),如亚乙基二胺,二亚乙基三胺,三亚乙基四胺,六亚甲基二胺,1,2-双(3-氨基丙基氨基)乙烷的反应产物,2-氯-4,6-双(4-正丁氨基-2,2,6,6-四甲基哌啶)-1,3,5-三嗪和4-叔辛氨基-2,6-二氯-1,3,5-均三嗪和单-或多-官能胺(其中胺上的一个至全部活性氢原子被置换),如亚乙基二胺,二亚乙基三胺,三亚乙基四胺,六亚甲基二胺,1,2-双(3-氨基丙基氨基)乙烷的反应产物,2-氯-4,6-双(4-正丁氨基-1,2,2,6,6-五甲基哌啶)-1,3,5-三嗪和4-叔辛氨基-2,6-二氯-1,3,5-均三嗪和单-或多-官能胺(其中胺上的一个至全部活性氢原子被置换),如亚乙基二胺,二亚乙基三胺,三亚乙基四胺,1,2-双(3-氨基丙基氨基)乙烷的反应产物,2-氯-4,6-双(4-正丁氨基-2,2,6,6-四甲基哌啶)-1,3,5-三嗪和4-(4-正丁氨基-2,2,6,6-四甲基哌啶)-2,6-二氯-1,3,5-均三嗪和单-或多-官能胺(其中胺上的一个至全部活性氢原子被置换),如亚乙基二胺,二亚乙基三胺,三亚乙基四胺,六亚甲基二胺,1,2-双(3-氨基丙基氨基)乙烷的反应产物,2-氯-4,6-双(4-正丁氨基-1,2,2,6,6-五甲基哌啶)-1,3,5-三嗪及4-(4-正丁氨基-2,2,6,6-四甲基哌啶)-2,6-二氯-1,3,5-均三嗪和单-或多-官能胺(其中胺上的一个至全部活性氢原子被置换),如亚乙基二胺,二亚乙基三胺,三亚乙基四胺,六亚甲基二胺,1,2-双(3-氨基丙基氨基)乙烷的反应产物,1,2-双(3-氨基丙基氨基)乙烷和2,4,6-三氯-1,3,5-三嗪的缩合物,以及4-丁氨基-2,2,6,6-四甲基哌啶,N-(2,2,6,6-四甲基-4-哌啶)-正-十二烷基琥珀酰胺,N-(1,2,2,6,6-五甲基-4-哌啶)-正-十二烷基琥珀酰胺,8-乙酰-3-十二烷基-7,7,9,9-四甲基-1,3,8-三氮杂螺[4.5]癸烷-2,4-二酮,寡聚化2,2,4,4-四甲基-20-(环氧乙烷甲基)-7-噁-3,20-二氮杂双螺[5.1.11.2]二十一烷-21-酮,寡聚化1,2,2,4,4-五甲基-20-(环氧乙烷甲基)-7-噁-3,20-二氮杂双螺[5.1.11.2]二十一烷-21-酮,寡聚化1-乙酰-2,2,4,4-四甲基-20-(环氧乙烷甲基)-7-噁-3,20-二氮杂双螺[5.1.11.2]二十一烷-21-酮,3-十二烷基-1-(2,2,6,6-四甲基-4-哌啶)吡咯烷-2,5-二酮,3-十二烷基-1-(1,2,2,6,6-五甲基-4-哌啶)吡咯烷-2,5-二酮,2,2,4,4-四甲基-7-噁-3,20-二氮杂双螺[5.1.11.2]二十一烷-21-酮,2,2,4,4-四甲基-7-噁-21-氧-3,20-二氮杂双螺[5.1.1 1.2]二十一烷-3-丙酸十二烷酯,2,2,4,4-四甲基-7-噁-21-氧-3,20-二氮杂双螺[5.1.11.2]二十一烷-3-丙酸十四烷酯,2,2,3,4,4-五甲基-7-噁-3,20-二氮杂双螺[5.1.11.2]二十一烷-21-酮,2,2,3,4,4-五甲基-7-噁-21-氧-3,20-二氮杂双螺[5.1.11.2]二十一烷-3-丙酸十二烷酯,2,2,3,4,4-五甲基-7-噁-21,氧-3,20-二氮杂双螺[5.1.11.2]二十一烷-3-丙酸十四烷酯,3-乙酰-2,2,4,4-四甲基-7-噁-3,20-二氮杂双螺[5.1.11.2]二十一烷-21-酮,3-乙酰-2,2,4,4-四甲基-7-噁-21-氧-3,20-二氮杂双螺[5.1.11.2]二十一烷-3-丙酸十二烷酯,3-乙酰-2,2,4,4-四甲基-7-噁-21-氧-3,20-二氮杂双螺[5.1.11.2 ]二十一烷-3-丙酸十四烷酯,1,1’,3,3’,5,5’-六氢-2,2,’,4,4’,6,6’-六氮杂-2,2’,6,6’-双亚甲基-7,8-二氧-4,4’-双(1,2,2,6,6-五甲基-4-哌啶)联苯,聚-N,N’-双(2,2,6,6-四甲基-4-哌啶)-1,8-二氮杂癸烯,2,2,6,6-四甲基-4-丙烯氧哌啶及聚甲氢硅氧烷的加成物(分子量高至4000),1,2,2,6,6-五甲基-4-丙烯氧哌啶及聚甲氢硅氧烷的加成物(分子量高至4000),N,N’-二甲酰-N,N’-双(2,2,6,6-四甲基-4-哌啶)六亚甲基二胺,N,N’-二甲酰-N,N’-双(1,2,2,6,6-五甲基-4-哌啶)六亚甲基二胺,5,11-双(2,2,6,6-四甲基-4-哌啶)-3,5,7,9,11,13-六氮杂四环[7.4.0.02,7,13,13]十四烷-8,14-二酮,5,11-双(1,2,2,6,6-五甲基-4-哌啶)-3,5,7,9,11,1 3-六氮杂四环[7.4.0.02,7,13,13]十四烷-8,14-二酮,[(4-甲氧苯)亚甲基]丙二酸双(2,2,6,6-四甲基-4-哌啶)酯,[(4-甲氧苯)亚甲基]丙二酸双(1,2,2,6,6-五甲基-4-哌啶)酯,2,4,6-三(N-环己基-N-[ 2-(3,3,4,5,5-五甲基哌嗪酮-1-基)乙基]氨基)-1,3,5-三嗪,苯乙烯和甲基苯乙烯和马来酸酐(与4-氨基-2,2,6,6-四甲基哌啶及十八烷胺反应过)的共聚物,苯乙烯和α-甲基苯乙烯及马来酸酐(与4-氨基-1,2,2,6,6-五甲基哌啶和十八烷反应过)的共聚物,以2,2’-[(2,2,6,6-四甲基-4-哌啶)亚氨基双[乙醇]为二醇成分的聚碳酸酯,含2,2’-(1,2,2,6,6-五甲基-4-哌啶)亚氨基]双[乙醇]为二醇成分的聚碳酸酯,马来酸酐和以4-氨基-2,2,6,6-四甲基哌啶反应过的高至C30的α-烯烃的共聚物,马来酸酐和以1-乙酰-4-氨基-2,2,6,6-四甲基哌啶反应过的高至C30的α-烯烃的共聚物,马来酸酐和以4-氨基-1,2,2,6,6-五甲基哌啶反应过的高至C30的α-烯烃的共聚物,以及上述化合物的在哌啶上具自由NH基的N-烷基-及N-芳氧基衍生物,特别是α-甲基苄氧基及C1-18烷氧基衍生物。
2.7草酰胺,如4,4’-二辛氧草酰替苯胺,2,2’-二乙氧基草酰替苯胺,2,2’-二辛氧-5,5’-双叔丁基草酰替苯胺,2,2’-双十二烷氧-5,5’-双叔丁基草酰替苯胺,2-乙氧-2’-乙基草酰替苯胺,N,N’-双(3-二甲胺丙基)草酰胺,2-乙氧-5-叔丁基-2’-乙基草酰替苯胺及其和2-乙氧-2’-乙基-5,4’-双叔丁基草酰替苯胺的混合物,以及邻-及对-甲氧基双取代和邻-及对-乙氧基双取代的草酰替苯胺的混合物。
2.8 2-(2-羟苯)-1,3,5-三嗪,如2,4,6-三-(2-羟-4-辛氧苯基)-1,3,5-三嗪,2-(2-羟-4-辛氧苯)-4’,6-双(2’,4-二甲基苯基)-1,3,5-三嗪,2-(2,4-二羟基苯基)-4,6-双(2,4-二甲基苯基)-1,3,5-三嗪,2-(2,4-二羟基苯基)-4,6-双(2,4-二甲基苯基)-1,3,5-三嗪,2,4-双(2-羟-4-丙氧基苯基)-6-(2,4-二甲基苯基)-1,3,5-三嗪,2-(2-羟-4-辛氧苯基)-4,6-双(4-甲苯基)-1,3,5-三嗪,2-(2-羟-4-十二烷氧基苯基)-4,6-双(2,4-二甲苯)-1,3,5-三嗪,2-[2-羟-4-(2-羟-3-丁氧基丙氧基苯基)苯基]-4,6-双(2,4-二甲基苯基)-1,3,5-三嗪,2-[2-羟-4-(2-羟-3-辛氧丙氧)苯]-4,6-双(2,4-二甲基苯基)-1,3,5-三嗪,2-(2-羟-4-十三烷氧苯)-4,6-双(2,4-二甲苯基)-1,3,5-三嗪,2-[4-(十二烷氧/十三烷氧-2-羟丙氧)-2-羟苯]-4,6-双(2,4-二甲基苯基)-1,3,5-三嗪,2-[2-羟-4-(2-羟-3-十二烷氧丙氧)苯]-4,6-双(2,4-二甲基苯基)-1,3,5-三嗪,2-(2-羟-4-己氧)苯-4,6-二苯-1,3,5-三嗪,2-(2-羟-4-甲氧苯)-4,6-二苯基-1,3,5-三嗪,2,4,6-三[2-羟-4-(3-丁氧-2-羟丙氧)苯]-1,3,5-三嗪,2-(2-羟苯)-4-(4-甲氧苯)-6-苯-1,3,5-三嗪。
3.金属钝化剂,如N,N’-二苯草酰胺,N-水杨醛-N’-水杨酰肼,N,N’-双(水杨酰)肼,N,N’-双(3,5-双叔丁基-4-羟苯丙酰)肼,3-水杨酰胺-1,2,4-三唑,双(苄叉)草酰二肼,草酰替苯胺,间苯二酰二肼,癸二酰二苯肼,N,N’-二乙酰己二酰二肼,N,N’-双(水杨酰)草酰二肼,N,N’-双(水杨酰)硫代丙酰二肼。
4.亚磷酸酯及亚膦酸酯,如亚磷酸三苯酯,亚磷酸二苯基烷基酯,亚磷酸苯二烷酯,亚磷酸三(壬苯)酯,亚磷酸三月桂酯,亚磷酸三(十八烷)酯,二亚磷酸二硬脂酰季戊四醇酯,亚磷酸三(2,4-双叔丁苯)酯,二亚磷酸二异癸基季戊四醇酯,二亚磷酸双(2,4-双叔丁苯)季戊四醇酯,二亚磷酸双(2,6-双叔丁基-4-甲苯)季戊四醇酯,二亚磷酸双异癸氧季戊四醇酯,二亚磷酸双(2,4-双叔丁基-6-甲苯)季戊四醇酯,二亚磷酸双(2,4,6-三叔丁苯)季戊四醇酯,三亚磷酸三硬脂基山梨糖醇酯,4,4’-亚联苯基二亚磷酸四(2,4-双叔丁苯)酯,6-异辛氧-2,4,8,10-四叔丁基-12H-二苯并[d.g]-1,3,2-二噁磷
(phosphocin),6-氟-2,4,8,10-四叔丁基-12-甲基-二苯并[d.g]-1,3,2-二噁磷
,亚磷酸双(2,4-双叔丁基-6-甲苯)甲酯,亚磷酸双(2,4-双叔丁基-6-甲苯)乙酯,亚磷酸三(2-叔丁基-4-硫(2’-甲基-4’-羟-5’-叔丁基)苯-5-甲基)苯酯,2,2’,2”-次氮基[三(3,3’,5,5’-四叔丁基-1,1’-二苯基-2,2’-二基)亚磷酸三乙酯],亚磷酸双[2-甲基-4,6-双(1,1-二甲乙基)苯酚]乙酯。
5.羟胺,如N,N-二苄羟胺,N,N-二乙基羟胺,N,N-二辛基羟胺,N,N-二月桂基羟胺,N,N-双十四烷羟胺,N,N-双十六烷烃胺,N,N-双十八烷烃胺,N-十六烷-N-十八烷羟胺,N-十七烷-N-十八烷羟胺,及由氢化牛脂肪胺所制的N,N-二烷羟胺。
6.硝酮,如N-苄-α-苯硝酮,N-乙基-α-甲基硝酮,N-辛基-α-庚基硝酮,N-月桂基-α-十一烷基硝酮,N-十四烷基-α-十三烷基硝酮,N-十六烷基-α-十五烷基硝酮,N-十八烷基-α-十七烷基硝酮,N-十六烷基-α-十七烷基硝酮,N-十八烷基-α-十五烷基硝酮,N-十七烷基-α-十七烷基硝酮,N-十八烷基-α-十六烷基硝酮,及由氢化牛脂肪胺所制的N,N-二烷羟胺所衍生的硝酮。
7.沸石及水滑石,如DHT 4A。此类水滑石可用下式表示:
[(M2+)1-x(M3+)x(OH)2(An-)x/nyH2O]
式中
(M2+)是Mg,Ca,Sr,Ba,Zn,Pb,Sn,Ni
(M3+)是Al,B,Bi
An是n价的阴离子
m是整数1至4
x是0至0.5的值
y是0至2的值
A是
OH-,Cl-,Br-,I-,ClO4 -,CH3COO-,C6H5COO-,CO3 2-,SO4 2-,(OOC-COO)2-,(CHOHCOO)2 2-,(CHOH)4CH2OHCOO-,C2H4(COO)2 2-,(CH2COO)2 2-,CH3CHOHCOO-,SiO3 2-,SiO4 4-,Fe(CN)6 3-,Fe(CN)6 4-,BO3 3-,PO3 3-,HPO4 2-,
优选为采用其中M2+是Ca2+,Mg2+或Mg2+和Zn2+的混合物;(An-)是CO3 2-,BO3 2-,PO3 3-;x为0至0.5的值,y为0至2的值的水滑石。亦可采用下式所示的水滑石:
[(M2+)x(All3+)2(OH)2x+6nz(An-)2yH2O]
式中
M2+是Mg2+,Zn2+,但更优选为Mg2+;
(An-)是阴离子,尤指CO3 2-,(OOC-COO)2-,OH-及S2-,其中n是阴离子的价位;
y是正数,更优选为0至5,特别是0.5至5;
x及z是正值,x优选为2至6,而z应小于2。
特别优选为下式的水滑石:
Al2O3×6MgO×CO2×12H2O,
Mg4.5Al2(OH)13×CO3×3.5H2O,
4MgO×Al2O3×CO2×9H2O,
4MgO×Al2O3×CO2×6H2O,
ZnO×3MgO×Al2O3×CO2×8-9H2O,
ZnO×3MgO×Al2O3×CO2×5-6H2O,
Mg4.5Al2(OH)13×CO3,
水滑石的用量优选占整个聚合物制剂重量的0.01至5%,特别为0.2至3%。
8.硫增效剂,如硫代二丙酸二月桂酯及硫代二丙酸二硬脂酯。
9.过氧化物清除剂,如β-硫二丙酸酯,例如月桂酯,硬脂酯,肉豆蔻酯或十三烷酯,巯苯并咪唑,2-巯苯并咪唑的锌盐,烷二硫代氨基甲酸锌,二丁基二硫代氨基甲酸锌,单硫化双十八烷,二硫化双十八烷、四(β-十二烷巯基)丙酸季戊四醇酯。
10.聚酰胺稳定剂,如铜盐联合碘化物和/或磷化物以及两价锰的盐。
11.碱性辅稳定剂,如蜜胺,聚乙烯吡咯烷酮,双氰胺,氰脲酸三丙烯酯,脲衍生物,肼衍生物,胺,聚胺,聚脲烷,高级脂肪酸的碱金属和碱土金属盐,如硬脂酸钙,硬脂酯锌,山萮酸镁,硬脂酸镁,蓖麻酸钠,棕榈酸钾,邻苯二酚锑或邻苯二酚锡,以及乳酸的碱金属及碱土金属盐,锌盐或铝盐。
12.成核剂,如无机物,例如滑石、金属氧化物,如氧化钛或氧化镁,优选为碱土金属的磷酸盐,碳酸盐或硫酸盐,有机物,如单-或多羧酸,及其盐,如4-叔丁基苯甲酸,己二酸,二苯醋酸;琥珀酸钠或苯甲酸钠;芳醛及多官能醇(如山梨糖醇)的缩合物,如1,3-2,4-双苄叉-D-山梨糖醇,1,3-2,4-双(4-甲苯叉)-D-山梨糖醇,1,3-2,4-双(4-乙基苄叉)-D-山梨糖醇;聚合化合物,如离子共聚物(离聚物)。
13.填充料及增强剂,如碳酸钙,硅酸盐,玻璃纤维,石棉,滑石,高领土,云母,硫酸钡,金属氧化物及金属氢氧化物,碳黑,石墨,木粉及其他天然产物的粉末或纤维,合成纤维。
14.其他添加剂,如增塑剂,润滑剂,乳化剂,颜料,流变添加剂,催化剂,均化助剂,亮光剂,阻燃剂,抗静电剂,发泡剂及颜色改良剂。
15.苯并呋喃酮及二氢吲哚,例如美国专利US-4,325,863,US-4,338,224号,US-5,175,312,US-5,216,052,US-5,252,643,德国专利DE-A-4,316,611,DE-A-4,316,622,DE-A-4,316,876,欧洲专利EP-A-0,589,839或EP-A-0,591,102所描述的,或3-[4-(2-乙酰氧乙氧)苯]-5,7-双叔丁基苯并呋喃-2-酮,5,7-双叔丁基-3-[4-(2-硬脂酰氧乙氧)苯]苯并呋喃-2-酮,3,3’-双[5,7-双叔丁基-3-(4-[2-羟乙氧基]苯基)苯并呋喃-2-酮,5,7-双叔丁基-3-(4-乙氧苯)苯并呋喃-2-酮,3-(4-乙酰氧-3,5-二甲苯)-5,7-双叔丁基苯并呋喃-2-酮,3-(3,5-二乙基-4-新戊酰氧苯)-5,7-双叔丁基苯并呋喃-2-酮。
本发明亦涉及纳米尺寸颗粒形式的前述添加剂。
以下面实施例对本发明进行说明。
实施例
使用了以下化合物:
化合物(a):Sandostab P-EPQ(Clariant)
四(2,4-二叔丁基苯基)-4,4’-亚联苯基双亚磷酸酯
化合物(b):5,7-双叔丁基-3-苯基-3H-苯并呋喃-2-酮
化合物(c):Hostavin N30(Clariant)
表氯醇和2,2,4,4-四甲基-7-氧杂-3,20-二氮杂-20-(2,3-环氧丙基)二螺[5.1.11.2]二十一烷-21-酮
化合物(d):Hostanox O 10(Clariant)
四[(亚甲基-3-(3’,5’)-双叔丁基-4’-羟基苯基)丙酸酯]甲烷
Tinuvin 622(Ciba SC)
聚(N-羟乙基-2,2,6,6-四甲基-4-羟哌啶基琥珀酸酯)
在下列说明中,“份数”指“重量份数”。
100份第三代聚丙烯(Moptell公司的MoplenFLF20,熔融流动指数(230℃/2.16千克):14.2克/10分钟),在加入0.025份三苯膦,0.025份化合物(b),0.020%化合物(c)和0.10份硬脂酸钙后,在280℃多次挤出。
在预挤出前,先将聚合物粉末与添加剂在实验室混合器(Kenwood型)中混合,然后用单螺杆挤压机(螺杆直径4毫米,Haendle公司的KPS-25)在210℃,80转/分钟转速进行预挤出。主挤出则用配有在线流变仪的单螺杆挤压机(螺杆压缩比1∶3,50转/分钟,模头直径2毫米,Gttfert Extrusimeter)在T=280℃下进行。依美国标准试验材料ASTM 1238(于230℃,2.16千克荷重),测定各单独试样的熔融流动指数。依德国工业规格DIN 6167,利用比色仪(Minolta公司)测量颜色。结果列于下列表1A及1B中,并与含有0.10份化合物(d)(具四官能的市售酚),0.05份化合物(a)及0.10份硬脂酸钙的制剂做比较。
表1A:熔融流动指数(MFI) | |||
稳定剂制剂(除酸剂:0.10%硬脂酸钙) | 第一次挤出 | 第三次挤出 | 第五次挤出 |
比较例:0.05份化合物(a)+0.10份化合物(d) | 13.22 | 16.85 | 22.27 |
本发明:0.025份三苯膦+0.025份化合物(b)+0.02份化合物(c) | 12.81 | 15.48 | 18.20 |
表1B:颜色(黄度指数YI) | |||
稳定剂制剂(除酸剂:0.10%硬脂酸钙) | 第一次挤出 | 第三次挤出 | 第五次挤出 |
比较例:0.05份化合物(a)+0.10份化合物(d) | 1.49 | 2.77 | 4.78 |
本发明:0.025份三苯膦+0.025份化合物(b)+0.02份化合物(c) | 0.27 | 0.51 | 1.34 |
聚丙烯的加工、曝晒及测试
在实验室混合器(Kenwood)中混合100重量份聚丙烯[PP,Himont公司的Moplen FLF20,内码PP97-4,熔融流动指数MFI 12克/10分钟(230℃/2.16千克荷重)],0.10重量份酚抗氧化剂(Hostanox O 10),0.10份硬脂酸钙,0.05份Sandostab P-EPQ。经加工后,此试样做为对照用。另外,采用的制剂包含0.02重量份空间位阻胺[HA(L)S],0.10重量份硬脂酸钙,0.04重量份5,7-二叔丁基-(3-苯基)-3H-苯并呋喃-2-酮(内酯)及0.01重量份三苯膦。其后利用单螺杆挤压机(Haendle公司的KPS25,螺杆压缩比1∶3,模头直径4毫米,螺杆速率80rpm)在220℃进行预挤出。主挤出(第一至第五次挤出)则利用单螺杆挤出机(G üttfert Extrusimeter,螺杆压缩比1∶3,100转/分,模头直径2毫米)进行,其中1个加热区为180℃,2个加热区为200℃及4个加热区各为210℃。经此加工步骤最后成为0.5-2.00毫米的颗粒。第一次及第五次挤出颗粒随后被送至实验室热压塑机(Fontjne TP600)上的框模(厚度0.5毫米)中。先选用210℃的板温,在50千牛顿的压力下压90秒,然后在500千牛顿压力下再压90秒。
依ASTM G26-90所述的步骤,利用氙弧灯耐候仪将所制的板进行人工长期曝晒(CAM-7)。利用红外光谱仪(FTS155)测量羰基吸收峰的形成状况,做为氧化降解重要的相关指标。此法主要是用于聚丙烯。实际的测量集中在要发展到羰基吸收Δ(>C=O)=1所需的滞留时间(小时)上。测量的是经第一次和第五次挤出的试样。结果列于表2。作为要达到附加羰基吸收Δ(>C=O)=1所给出时间值外的补充,还用“延长因数”(PF)来反映各单独稳定剂系统的效率。
测量的时间越长及延长因数越大,表示稳定剂系统的效率越高。
由表2的数据可明显的看出,含0.01%三苯膦、0.04%5,7-双叔丁基-(3-苯基)-3H-苯并呋喃-2-酮(表2中的“内酯”)和0.02%Hostavin N30的制剂优于其他制剂,尤其优于传统含酚的对照制剂。
表2
挤出次数 | 稳定剂制剂 | Δ(>C=O)=1/hr | 延长因数 |
1 | 0.05%Sandostab P-EPQ,0.10%Hostanox O 10,(对照) | 317 | 1 |
5 | 0.05%Sandostab P-EPQ,0.10%Hostanox O 10,(对照) | 293 | 1 |
1 | 0.01%三苯膦0.04%内酯0.02%Tinuvin 622 | 911 | 2.874 |
5 | 0.01%三苯膦0.04%内酯0.02%Tinuvin 622 | 868 | 2.962 |
1 | 0.01%三苯膦0.04%内酯0.02%Hostavin N30 | 1098 | 3.464 |
5 | 0.01%三苯膦0.04%内酯0.02%Hostavin N30 | 1149 | 3.921 |
Claims (6)
1.一种用于热塑性聚合物的稳定剂组合物,包含
a)至少一种有机膦,
b)至少一种2-苯基苯并呋喃酮,及
c)至少一种基于空间位阻哌啶的稳定剂,
其中成分a)对成分b)对成分c)的重量比为从1∶0.05∶0.5到1∶3∶5。
2.如权利要求1所述的稳定剂组合物,包含
a)式(I)到(IV)的至少一种化合物
其中各自独立的
R1是C1-24烷基或包含一个或多个选自N、O、P和S的杂原子的C1-24杂烷基、C5-30环烷基或包含一个或多个选自N、O、P和S的杂原子的C5-30杂环烷基、C7-30烷芳基、C6-24芳基、包含一个或多个选自N、O、P和S的杂原子的C4-24杂芳基、C6-24芳基或包含一个或多个选自N、O、P和S的杂原子的C4-24杂芳基,其被C1-18烷基、C5-12环烷基或C1-18烷氧基所单-或多-取代;
R2是C4-24烷基或包含一个或多个选自N、O、P和S的杂原子的C4-24杂烷基、C5-30环烷基或包含一个或多个选自N、O、P和S的杂原子的C5-30杂环烷基、C7-30烷芳基、C6-24芳基、包含一个或多个选自N、O、P和S的杂原子的C4-24杂芳基、C6-24芳基或包含一个或多个选自N、O、P和S的杂原子的C4-24杂芳基,其被C1-18烷基、C5-12环烷基或C1-18烷氧基所单-或多-取代;
D是直链或支链的C1-30亚烷基或包含一个或多个选自N、O、P和S的杂原子的C1-30亚烷基、C2-30烷叉基或包含一个或多个选自N、O、P和S的杂原子的C2-30烷叉基、C5-12亚环烷基或包含一个或多个选自N、O、P和S的杂原子的C5-12亚环烷基、C6-24亚芳基或包含一个或多个选自N、O、P和S的杂原子的C4-24亚杂芳基,其未被取代或被直链或支链的C1-18烷基、C5-12环烷基或C1-18烷氧基所单-或多-取代,或-O-、-S-;
q是1至5;
r是3至6,其中式(IV)中的P-R2基为磷杂环的成分,以由P引出的键中的*号表示;
b)至少一种式(V)的化合物:
其中Ra、Rb、Rd、Re、Rf、Rg及Rh各自独立为氢、羟基、C1-18烷基、或未被取代或被C1-4烷基所单-、双-或三-取代的苯基、未被取代或被C1-4烷基所单-、双-或三-取代的C7-9苯烷基、C1-18烷氧基或C5-12环烷基,且
Rc具有为前面Ra、Rb、Rd、Re、Rf、Rg及Rh给出的一种定义,或为式(VI)的基团:
式中Ra、Rb、Rd、Re、Rf、Rg及Rh如前面所定义,和Ri和Rj各自独立地为氢或C1-4烷基,其中Rd、Re、Rf、Rg和Rh至少有两个是氢;和
c)至少一种式(VII)的空间位阻胺化合物:
式中,X1为氢、C1-22烷基、氧自由基O*、-OH、-NO、-CH2CN、苄基、烯丙基、C1-30烷氧基、C5-12环烷氧基、C6-10芳氧基、C7-20芳烷氧基或其中芳基被C1-5烷基、卤原子或硝基所取代的C7-20芳烷氧基,C3-10烯基、C3-6炔基、C1-10酰基、卤素、未被取代或被C1-4烷基取代的苯基;
X2是氢、[CH2-CH2-C(O)-O-X5]基、[CH2-C(CH3)H-C(O)-O-X5]基、C1-22烷基;
X3和X4各自独立地为氢、未被取代或被C1-4烷基取代的苯基;或C1-22烷基,其中X3和X4中至少有一个为支链C4-22烷基;且其中
X5是C1-22烷基。
3.如权利要求2的稳定剂组合物,其中:
R1是C8-24烷基或包含一个或多个选自N、O、P和S的杂原子的C8-24杂烷基;C6-12环烷基或包含一个或多个选自N、O、P和S的杂原子的C6-12杂环烷基;C7-24烷芳基;C6-16芳基;包含一个或多个选自N、O、P和S的杂原子的C4-18杂芳基;C6-16芳基或包含一个或多个选自N、O、P和S的杂原子的C4-18杂芳基,其被C1-12烷基、C5-8环烷基或C1-12烷氧基所单-或多-取代;
R2是C6-18烷基或包含一个或多个选自N、O、P和S的杂原子的C6-18杂烷基;C5-12环烷基或包含一个或多个选自N、O、P和S的杂原子的C5-12杂环烷基;C7-18烷芳基;C6-16芳基;包含一个或多个选自N、O、P和S的杂原子的C4-18杂芳基;C6-16芳基或包含一个或多个选自N、O、P和S的杂原子的C4-18杂芳基,其可被C1-12烷基;C5-8环烷基或C1-12烷氧基所单-或多-取代;
D是直链或支链的C1-24亚烷基或包含一个或多个选自N、O、P和S的杂原子的C1-24亚烷基;C2-24烷叉基或包含一个或多个选自N、O、P和S的杂原子的C2-24烷叉基;C5-8亚环烷基或包含一个或多个选自N、O、P和S的杂原子的C5-8亚环烷基;C6-24亚芳基或包含一个或多个选自N、O、P和S的杂原子的C4-18亚杂芳基,其是未被取代的或被一或多个直链或支链C1-18烷基,C5-8环烷基,C1-24烷氧基所取代;-O-;-S-;
q是1至4;
r是4或5,其中式(IV)中的P-R2基为磷杂环的成分,以由P引出的键中的*号表示;
Ra、Rb、Rd、Re、Rf、Rg及Rh各自独立地是氢;羟基;C1-12烷基;或未被取代或被C1-2烷基所单-、双-或三-取代的苯基;C7-9苯烷基;C1-12烷氧基或C5-8环烷基,其是未被取代的或被C1-2烷基所单-、双-或三-取代;和Rc具有前面为Ra、Rb、Rd、Re、Rf、Rg及Rh所给出的一种定义或是式(VI)的基团,其中
Ra、Rb、Rd、Re、Rf、Rg及Rh如前述的定义,Ri、Rj各自独立地是氢或C1-2烷基,其中Rd、Re、Rf、Rg及Rh中有至少两个是氢;
X1是氢;C1-5烷基;氧自由基O*;-OH;-NO;-CH2CN;苄基;烯丙基;C1-10烷氧基;C5-6环烷氧基;C6-7芳氧基;C7-10芳烷氧基或其中芳基被C1-5烷基、卤素或硝基取代的C7-10芳烷氧基;C3-6烯基;C3-6炔基;C1-5酰基;卤素;未被取代或被C1-2烷基取代的苯基;
X2是氢;[CH2-CH2-C(O)-O-X5]基;[CH2-C(CH3)H-C(O)-O-X5]基;C1-10烷基;
X3及X4各自独立地是氢;未被取代或被C1-2烷基取代的苯基;或支链的C4-22烷基,且X3及X4中至少有一个为支链C4-10烷基;且其中
X5是C10-16烷基。
4.如权利要求2的稳定剂组合物,其中
R1是C12-16烷基或包含一个或多个选自N、O、P和S的杂原子的C12-16杂烷基;C6-8环烷基或包含一个或多个选自N、O、P和S的杂原子的C6-8杂环烷基;C7-12烷芳基;C6-12芳基或包含一个或多个选自N、O、P和S的杂原子的C4-10杂芳基;C6-12芳基或C4-10杂芳基,其被C1-18烷基,C5-6环烷基或C1-8烷氧基所单-或多-取代;
R2是C8-18烷基或包含一个或多个选自N、O、P和S的杂原子的C8-18杂烷基;C5-8环烷基或包含一个或多个选自N、O、P和S的杂原子的C5-8杂环烷基;C7-12烷芳基;C6-12芳基;包含一个或多个选自N、O、P和S的杂原子的C4-10杂芳基;C6-12芳基或包含一个或多个选自N、O、P和S的杂原子的C4-10杂芳基,其被C1-8烷基,C5-6环烷基或C1-8烷氧基所单或多取代;
D是直链或支链的C1-18亚烷基或包含一个或多个选自N、O、P和S的杂原子的C1-18亚烷基;C2-18烷叉基或包含一个或多个选自N、O、P和S的杂原子的C2-18烷叉基;C5-8亚环烷基或包含一个或多个选自N、O、P和S的杂原子的C5-8亚环烷基;未被取代或被直链或支链C1-12烷基,C5-8环烷基或C1-8烷氧基所单或多取代的C6-18亚芳基或包含一个或多个选自N、O、P和S的杂原子的C4-18亚杂芳基;或-O-;-S-;
q是1至3;
r是4或5,其中式(IV)中的P-R2基为磷杂环的成分,以由P引出的键中的*号表示;
Ra、Rb、Rd、Re、Rf、Rg及Rh各自独立地是氢、羟基、C1-6烷基、或未被取代或被C1-2烷基所单-、双-或三-取代的苯基;C7-9苯烷基、C1-6烷氧基或C5-8环烷基,其是未被取代的或被C1-2烷基所单-、双-或三-取代;Rc具有前面为Ra、Rb、Rd、Re、Rf、Rg及Rh所给出的一种定义或为式(VI)的基团,其中
Ra、Rb、Rd、Re、Rf、Rg及Rh如前所定义且Ri、Rj各自独立地是氢或C1-2烷基,且Rd、Re、Rf、Rg及Rh中至少有两个是氢;
X1是氢;甲基;氧自由基O*;-OH;-NO;-CH2CN;苄基;烯丙基;C1-6烷氧基,C5-6环烷氧基;C6芳氧基;C3-6烯基;C3-6炔基;C1-5酰基;卤素;未被取代或被C1-2烷基取代的苯基;
X2是氢,[CH2-CH2-C(O)-O-X5]基,[CH2-C(CH3)H-C(O)-O-X5]基、C1-4烷基;
X3及X4各自独立地是氢,未被取代或被C1-2烷基取代的苯基或支链的C4-6烷基,且X3及X4中至少有一个为支链的C4-6烷基;且其中
X5是C12-14烷基。
5.如权利要求1的稳定剂组合物,包含
a)三苯膦,
b)2-苯基苯并呋喃酮及
c)表氯醇和2,2,4,4-四甲基-7-氧杂-3,20-二氮杂-20-(2,3-环氧丙基)-二螺[5.1.11.2]-二十一烷-21-酮的聚合物,
其中成分a)对成分b)对成分c)的重量比为从1∶0.1∶1到1∶1∶3。
6.一种稳定热塑性聚合物的方法,其是在所要稳定的聚合物中加入0.01至1重量%的如权利要求1至5中任一项的稳定剂组合物。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0119136.0 | 2001-08-06 | ||
GBGB0119136.0A GB0119136D0 (en) | 2001-08-06 | 2001-08-06 | Phenolfree stabilizaton of polyolefins |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1538987A CN1538987A (zh) | 2004-10-20 |
CN1239591C true CN1239591C (zh) | 2006-02-01 |
Family
ID=9919885
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB028155130A Expired - Fee Related CN1239591C (zh) | 2001-08-06 | 2002-08-05 | 稳定剂组合物和稳定热塑性聚合物的方法 |
Country Status (13)
Country | Link |
---|---|
US (1) | US7105590B2 (zh) |
EP (1) | EP1417257B1 (zh) |
JP (1) | JP2005526146A (zh) |
KR (1) | KR100851177B1 (zh) |
CN (1) | CN1239591C (zh) |
AT (1) | ATE288937T1 (zh) |
DE (1) | DE60202959T2 (zh) |
ES (1) | ES2236556T3 (zh) |
GB (1) | GB0119136D0 (zh) |
HU (1) | HUP0401150A2 (zh) |
MX (1) | MXPA04001085A (zh) |
TW (1) | TW593490B (zh) |
WO (1) | WO2003014213A1 (zh) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7470735B2 (en) * | 2001-03-02 | 2008-12-30 | Dover Chemical Corporation | Phenol-free phosphites |
EP1462478A1 (en) * | 2003-03-26 | 2004-09-29 | Clariant International Ltd. | Improved long term dimensional stability of pigmented polymer articles |
AR053319A1 (es) * | 2004-12-22 | 2007-05-02 | Clariant Int Ltd | Mezclas de fosfinas con antioxidantes fenolicos liquidas o de baja fusion |
WO2009030708A1 (en) * | 2007-09-04 | 2009-03-12 | Basf Se | Cyclic phosphines as flame retardants |
DE602007008925D1 (de) * | 2007-12-21 | 2010-10-14 | Borealis Tech Oy | Polyolefinzusammensetzung für Mitte-/Hoch-/Höchstspannungskabel mit verbesserter elektrischer Durchbruchfestigkeit |
BR112017002203B1 (pt) * | 2014-08-05 | 2021-10-26 | Basf Se | Composição, processo para proteção de um material orgânico susceptível à degradação oxidativa, térmica ou induzida pela luz, uso de um composto de fórmula ip, i-o ou i-m, e, composto |
EP3578599A1 (en) | 2018-06-08 | 2019-12-11 | Cytec Industries Inc. | Granular stabilizer compositions for use in polymer resins and methods of making same |
WO2023003339A1 (ko) | 2021-07-20 | 2023-01-26 | 아주대학교산학협력단 | 세포 내부에 침투하여 표적단백질을 분해하여 제거하는 세포침투 분해항체 및 이의 용도 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4347602A (en) | 1978-05-31 | 1982-08-31 | Vdo Adolf Schindling Ag | Circuit arrangement for time division multiplex data transmission with a bus system |
US5616636A (en) | 1992-03-11 | 1997-04-01 | Sandoz Ltd. | Phosphonite-hals and phosphite-hals compounds as stabilizers |
US6153676A (en) | 1992-08-17 | 2000-11-28 | Clariant Finance (Bvi) Limited | Stabilized polyolefins |
US6593485B1 (en) | 1994-10-06 | 2003-07-15 | Clariant Finance (Bvi) Limited | Stabilizer composition |
US6521681B1 (en) | 1996-07-05 | 2003-02-18 | Ciba Specialty Chemicals Corporation | Phenol-free stabilization of polyolefin fibres |
GB2322374B (en) | 1997-02-21 | 2001-04-04 | Ciba Sc Holding Ag | Stabilizer mixture for organic materials |
ES2149678B1 (es) * | 1997-03-06 | 2001-05-16 | Ciba Sc Holding Ag | Estabilizacion de policarbonatos, poliesteres y policetonas. |
US5969014A (en) | 1997-09-23 | 1999-10-19 | Clariant Finance (Bvi) Limited | Synergistic polyamide stabilization method |
DE19942396A1 (de) * | 1999-09-06 | 2001-03-08 | Bayer Ag | Formmassen |
-
2001
- 2001-08-06 GB GBGB0119136.0A patent/GB0119136D0/en not_active Ceased
-
2002
- 2002-08-05 MX MXPA04001085A patent/MXPA04001085A/es active IP Right Grant
- 2002-08-05 WO PCT/IB2002/003062 patent/WO2003014213A1/en active IP Right Grant
- 2002-08-05 US US10/486,133 patent/US7105590B2/en not_active Expired - Fee Related
- 2002-08-05 JP JP2003519154A patent/JP2005526146A/ja active Pending
- 2002-08-05 ES ES02755421T patent/ES2236556T3/es not_active Expired - Lifetime
- 2002-08-05 EP EP02755421A patent/EP1417257B1/en not_active Expired - Lifetime
- 2002-08-05 AT AT02755421T patent/ATE288937T1/de not_active IP Right Cessation
- 2002-08-05 KR KR1020047001784A patent/KR100851177B1/ko not_active IP Right Cessation
- 2002-08-05 TW TW091117575A patent/TW593490B/zh not_active IP Right Cessation
- 2002-08-05 CN CNB028155130A patent/CN1239591C/zh not_active Expired - Fee Related
- 2002-08-05 HU HU0401150A patent/HUP0401150A2/hu unknown
- 2002-08-05 DE DE60202959T patent/DE60202959T2/de not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
TW593490B (en) | 2004-06-21 |
KR100851177B1 (ko) | 2008-08-08 |
ATE288937T1 (de) | 2005-02-15 |
US20040186207A1 (en) | 2004-09-23 |
KR20040024610A (ko) | 2004-03-20 |
EP1417257B1 (en) | 2005-02-09 |
HUP0401150A2 (hu) | 2004-09-28 |
JP2005526146A (ja) | 2005-09-02 |
DE60202959T2 (de) | 2006-03-16 |
CN1538987A (zh) | 2004-10-20 |
DE60202959D1 (de) | 2005-03-17 |
WO2003014213A1 (en) | 2003-02-20 |
GB0119136D0 (en) | 2001-09-26 |
MXPA04001085A (es) | 2004-07-08 |
US7105590B2 (en) | 2006-09-12 |
EP1417257A1 (en) | 2004-05-12 |
ES2236556T3 (es) | 2005-07-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1079809C (zh) | 协同稳定剂混合物 | |
CN1314739C (zh) | 对热、氧化或光致降解稳定的组合物、稳定混合物及其制备方法 | |
CN1082066C (zh) | 协同稳定剂混合物 | |
CN1165585C (zh) | 具有增强效果的包括添加剂共混物的合成聚合物 | |
CN1074014C (zh) | 合成有机聚合物的稳定剂混合物 | |
CN1196740C (zh) | 滚塑法用稳定剂组合 | |
CN1079808C (zh) | 协同稳定剂混合物 | |
CN1602334A (zh) | 阻燃剂组合物 | |
CN1860167A (zh) | 光致变色体系的稳定化 | |
CN1823127A (zh) | 阻燃性聚乳酸 | |
CN1106396C (zh) | 可用作有机材料的稳定剂的含有1-烃氧基-2,2,6,6-四甲基-4-哌啶基基团的嵌段低聚物 | |
CN1087287C (zh) | 包含苯酚基团和芳香胺基团的抗氧化剂 | |
CN1239591C (zh) | 稳定剂组合物和稳定热塑性聚合物的方法 | |
CN1222565C (zh) | 稳定剂混合物 | |
CN1969003A (zh) | 用于聚酯改性的含聚苯乙烯的母料组合物 | |
CN1685003A (zh) | 阻燃剂组合物 | |
CN1135477A (zh) | 双酚酯衍生物 | |
CN1074776C (zh) | 2,4-二甲基-6-仲-烷基酚和空间位阻酚组成的增效混合物 | |
CN1235959C (zh) | 稳定剂混合物 | |
CN1656163A (zh) | 稳定的制品 | |
CN1252160C (zh) | 用于与水长期接触的颜色稳定的有色热塑聚合物的协合稳定剂组合物 | |
CN1106398C (zh) | 可用作有机材料稳定剂的含有1-烃氧基-2,2,6,6-四甲基-4-哌啶基基团的嵌段低聚物 | |
CN1509299A (zh) | 用羟胺酯将烯属不饱和羧酸衍生物接枝到热塑性聚合物上的方法 | |
CN1257863A (zh) | 立体位阻胺化合物 | |
CN1214028C (zh) | 可用作有机材料的稳定剂的含有1-烃氧基-2,2,6,6-四甲基-4-哌啶基基团的嵌段低聚物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20060201 Termination date: 20100805 |