TW201546242A - 用於穩定物質抵抗紫外光與熱降解的穩定組合物 - Google Patents
用於穩定物質抵抗紫外光與熱降解的穩定組合物 Download PDFInfo
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- TW201546242A TW201546242A TW104113983A TW104113983A TW201546242A TW 201546242 A TW201546242 A TW 201546242A TW 104113983 A TW104113983 A TW 104113983A TW 104113983 A TW104113983 A TW 104113983A TW 201546242 A TW201546242 A TW 201546242A
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- Prior art keywords
- bis
- triazine
- tetramethyl
- ester
- hydroxy
- Prior art date
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- ZQTNRPACXQSETI-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-[2-(2-ethylhexoxy)ethoxy]phenol Chemical compound C1(=CC=CC=C1)C1=NC(=NC(=N1)C1=CC=CC=C1)C1=C(C=C(C=C1)OCCOCC(CCCC)CC)O ZQTNRPACXQSETI-UHFFFAOYSA-N 0.000 claims description 3
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- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 3
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- VVRICXZSRXFRSD-UHFFFAOYSA-N 5-oxo-5-(3,3,7,7-tetramethyl-5-piperidin-1-yltetradecan-2-yl)oxypentane-1,2,3-tricarboxylic acid Chemical compound OC(=O)CC(C(O)=O)C(C(O)=O)CC(=O)OC(C)C(C)(C)CC(CC(C)(C)CCCCCCC)N1CCCCC1 VVRICXZSRXFRSD-UHFFFAOYSA-N 0.000 claims description 3
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- ATLDIFPKVZGICS-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCCC)OC1CC(N(C(C1)(C)C)OCC(C)(C)OCCCCCCCCCCCCCCCCCC)(C)C Chemical compound C(CCCCCCCCCCCCCCCCC)OC1CC(N(C(C1)(C)C)OCC(C)(C)OCCCCCCCCCCCCCCCCCC)(C)C ATLDIFPKVZGICS-UHFFFAOYSA-N 0.000 claims description 3
- IBAFFORLAFBENJ-UHFFFAOYSA-N CCCCCCCCCCOCC(COC1=C(C=C(C(=C1)O)C2=NC(=NC(=N2)C3=C(C=C(C=C3)C)C)C4=C(C=C(C=C4)C)C)C(C)C)O Chemical compound CCCCCCCCCCOCC(COC1=C(C=C(C(=C1)O)C2=NC(=NC(=N2)C3=C(C=C(C=C3)C)C)C4=C(C=C(C=C4)C)C)C(C)C)O IBAFFORLAFBENJ-UHFFFAOYSA-N 0.000 claims description 3
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- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
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- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 3
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- AGHHRSWORINRIV-UHFFFAOYSA-N 1-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CN2C(NC(=O)NC2=O)=O)=C1 AGHHRSWORINRIV-UHFFFAOYSA-N 0.000 claims description 2
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- QSRJVOOOWGXUDY-UHFFFAOYSA-N 2-[2-[2-[3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoyloxy]ethoxy]ethoxy]ethyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C)=CC(CCC(=O)OCCOCCOCCOC(=O)CCC=2C=C(C(O)=C(C)C=2)C(C)(C)C)=C1 QSRJVOOOWGXUDY-UHFFFAOYSA-N 0.000 claims description 2
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- POHXPVPPMDIIOA-UHFFFAOYSA-N 2-[4-[4-[4-(2-acetyloxyethoxy)-2-hydroxyphenyl]-6-(4-chlorophenyl)-1,3,5-triazin-2-yl]-3-hydroxyphenoxy]ethyl acetate Chemical compound OC1=CC(OCCOC(=O)C)=CC=C1C1=NC(C=2C=CC(Cl)=CC=2)=NC(C=2C(=CC(OCCOC(C)=O)=CC=2)O)=N1 POHXPVPPMDIIOA-UHFFFAOYSA-N 0.000 claims description 2
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- TWCIEIJAAYQZQZ-UHFFFAOYSA-N 3-[4,4-bis(1,2,2,6,6-pentamethylpiperidin-4-yl)butoxy]-2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-3-oxopropanoic acid Chemical compound C1C(C)(C)N(C)C(C)(C)CC1C(C1CC(C)(C)N(C)C(C)(C)C1)CCCOC(=O)C(C(O)=O)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 TWCIEIJAAYQZQZ-UHFFFAOYSA-N 0.000 claims description 2
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- YAWARMNTAGPPGS-UHFFFAOYSA-N 5-(3-butoxy-2-hydroxypropoxy)-2-[3-[[6-[4-(3-butoxy-2-hydroxypropoxy)-2-hydroxyphenyl]-2,4-bis(2,4-dimethylphenyl)-2H-1,3,5-triazin-1-yl]methyl]-2,6-bis(2,4-dimethylphenyl)-2H-1,3,5-triazin-4-yl]phenol Chemical compound OC1=CC(OCC(O)COCCCC)=CC=C1C1=NC(C=2C(=CC(C)=CC=2)C)=NC(C=2C(=CC(C)=CC=2)C)N1CN1C(C=2C(=CC(OCC(O)COCCCC)=CC=2)O)=NC(C=2C(=CC(C)=CC=2)C)=NC1C1=CC=C(C)C=C1C YAWARMNTAGPPGS-UHFFFAOYSA-N 0.000 claims description 2
- YPFBPAKTPNIEJE-UHFFFAOYSA-N 5-(3-butoxy-2-hydroxypropoxy)-2-[4-[4-(3-butoxy-2-hydroxypropoxy)-2-hydroxyphenyl]-6-(2,4,6-trimethylphenyl)-1,3,5-triazin-2-yl]phenol Chemical compound OC1=CC(OCC(O)COCCCC)=CC=C1C1=NC(C=2C(=CC(OCC(O)COCCCC)=CC=2)O)=NC(C=2C(=CC(C)=CC=2C)C)=N1 YPFBPAKTPNIEJE-UHFFFAOYSA-N 0.000 claims description 2
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- VUYDRQJVUXIOHH-UHFFFAOYSA-N C(C(C(CC(=O)O)C(=O)O)C(=O)O)C(=O)OC1CC(N(C(C1)(C)C)C)(C)C.NN Chemical compound C(C(C(CC(=O)O)C(=O)O)C(=O)O)C(=O)OC1CC(N(C(C1)(C)C)C)(C)C.NN VUYDRQJVUXIOHH-UHFFFAOYSA-N 0.000 claims description 2
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- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- RSOILICUEWXSLA-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(C)C(C)(C)C1 RSOILICUEWXSLA-UHFFFAOYSA-N 0.000 claims description 2
- OSIVCXJNIBEGCL-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-octoxypiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(OCCCCCCCC)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(OCCCCCCCC)C(C)(C)C1 OSIVCXJNIBEGCL-UHFFFAOYSA-N 0.000 claims description 2
- VYCDFODYRFOXDA-UHFFFAOYSA-N bis(2,2,6,6-tetramethyl-1-undecoxypiperidin-4-yl) carbonate Chemical compound C1C(C)(C)N(OCCCCCCCCCCC)C(C)(C)CC1OC(=O)OC1CC(C)(C)N(OCCCCCCCCCCC)C(C)(C)C1 VYCDFODYRFOXDA-UHFFFAOYSA-N 0.000 claims description 2
- 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 claims description 2
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- OBQVOBQZMOXRAL-UHFFFAOYSA-L magnesium;docosanoate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCCCCCC([O-])=O OBQVOBQZMOXRAL-UHFFFAOYSA-L 0.000 claims description 2
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- RDDGGSBCDBLPDO-UHFFFAOYSA-N octadecyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C)=C(O)C(C(C)(C)C)=C1 RDDGGSBCDBLPDO-UHFFFAOYSA-N 0.000 claims description 2
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Classifications
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- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/527—Cyclic esters
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
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- 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
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
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- 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
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
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- 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
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Abstract
本文揭示用於穩定物質抵抗因熱及紫外光曝露所引起之降解之穩定劑組合物。在一些情況下,該穩定劑組合物包含鄰-羥基參-芳基-s-三嗪化合物;受阻胺光穩定劑化合物;受阻羥基苯甲酸酯化合物;亞磷酸酯化合物、酸清除劑及/或硫酯;及受阻酚抗氧化劑化合物。
Description
本發明係關於穩定組合物。特定言之,本發明係關於用於穩定物質抵抗紫外光降解與熱降解之組合物。
已知,曝露至陽光及其他紫外(UV)輻射源(亦稱為UV光)會導致眾多物質降解。例如,聚合物質(諸如塑膠)常常由於長期曝露至UV光而變色、失去光澤及/或變脆,主要係因為聚合物之分子量下降。因此,已研發許多針對組合物(諸如UV光吸收劑及穩定劑)之技藝,該等組合物可抑制聚合物件之此類降解。
亦已知,曝露至熱會導致物質,特別係聚合物質降解。雖然已研發出可減少或防止因熱所引起之降解之聚合物,但將此等組合物與UV光穩定劑之組合並非始終取得所需結果,因為在與該(等)熱穩定劑組合物組合時,UV光穩定性質通常受阻或完全喪失(relinquished)(亦即,拮抗)。因此,市面上仍需可防止物質因UV光及熱曝露而引起之降解之穩定劑組合物。據信,本發明將滿足上述需求。
在一態樣中,本發明係關於包含鄰-羥基參-芳基-s-三嗪化合物;受阻胺光穩定劑化合物;受阻羥基苯甲酸酯化合物;酸清除劑;亞磷
酸酯化合物;及受阻酚抗氧化劑化合物之熱及紫外(UV)光穩定組合物。
本發明之另一態樣係關於包含鄰-羥基參-芳基-s-三嗪化合物;受阻胺光穩定劑化合物;受阻羥基苯甲酸酯化合物;亞磷酸酯化合物及酸清除劑或硫酯之熱及紫外(UV)光穩定組合物。
在另一態樣中,本發明係關於包含本文所述任何熱及UV光穩定組合物及待穩定之物質之穩定組合物。
在另一態樣中,本發明係關於用於製備上述穩定組合物之方法,其中將該待穩定之物質與本文所述任何熱及UV光穩定組合物組合。
在又另一態樣中,本發明係關於一種用於改良選自以下組成之群之物質之可加工性之方法:聚烯烴、聚酯、聚醚、聚酮、聚醯胺、天然及合成橡膠、聚胺基甲酸酯、聚苯乙烯、耐衝擊(high-impact)聚苯乙烯、聚丙烯酸酯、聚甲基丙烯酸酯、聚縮醛、聚丙烯腈、聚丁二烯、聚苯乙烯、丙烯腈-丁二烯-苯乙烯、苯乙烯丙烯腈、丙烯酸酯苯乙烯丙烯腈、乙酸丁酸纖維素、纖維素聚合物、聚醯亞胺、聚醯胺醯亞胺、聚醚醯亞胺、聚苯硫醚、聚苯醚聚碸、聚醚碸、聚氯乙烯、聚碳酸酯、聚酮、脂族聚酮、熱塑性烯烴、胺基樹脂交聯聚丙烯酸酯及聚酯、聚異氰酸酯交聯聚酯及聚丙烯酸酯、苯酚/甲醛、脲/甲醛及三聚氰胺/甲醛樹脂、乾燥及非乾燥醇酸樹脂、醇酸樹脂、聚酯樹脂、與三聚氰胺樹脂、尿素樹脂、異氰酸酯、異氰尿酸酯、胺基甲酸酯及環氧樹脂交聯之丙烯酸酯樹脂、衍生自脂族、環脂族、雜環及芳族縮水甘油基化合物(其與酐或胺交聯)之交聯環氧樹脂、聚矽氧烷、邁克爾(Michael)加成聚合物、胺、具有活性不飽和及亞甲基化合物之封端胺、具有活性不飽和及亞甲基化合物之酮亞胺、與不飽和丙烯酸系聚乙醯乙酸酯樹脂組合之聚酮亞胺、與不飽和丙烯酸系樹脂組合之聚酮
亞胺、輻射可固化組合物、環氧三聚氰胺樹脂、有機染料、化妝品、纖維素基紙調配物、照相軟片紙、纖維、蠟、油墨及其摻合物,該方法包括向該物質添加穩定量之如本文所述穩定組合物。
本文更詳細地描述本發明之此等及其他態樣。
圖1A-1E為顯示含有與或未與光穩定組合物摻合之熱塑性烯烴之飾板在曝露至極端熱條件後之光澤保留性百分比之照片(分別對應表3之實例1C、2C、10、13及14)。
圖2為顯示實例15-19之結果之圖表。
如上所概述,與當前市售穩定劑包裝相比,出乎意料地,本文現首次已發現並揭示之組合物及其使用方法可用於達成抵抗熱及UV光降解之最佳穩定性。此外,本文所揭示之方法及組合物額外(及出乎意料地)提供相比於當前市售聚合物穩定劑包裝具有低揮發性有機化合物(VOC)釋放、低臭味及低溢流(blooming)之穩定劑包裝。
如上文及整個揭示內容所使用,提供以下術語及定義協助讀者。除非另有定義,否則希望本文所使用之技術術語、注釋及其他科學術語具有熟習化學技術者通常所理解之含義。如本文及隨附申請專利範圍中所使用,除非上下文另有明確規定,否則單數形式包括複數參考項。此外,如本文及隨附申請專利範圍中所使用,揭示任何用量或濃度範圍包括揭示給定範圍內之任何用量或數值。
在整個說明書內,術語及取代基保有其定義。有機化學工作者(亦即,一般技術者)所使用之縮寫之詳盡清單出現在Journal of Organic Chemistry各卷的第一期內。通常在標題為「標準縮寫清單」之表格中提供之清單係以引用的方式併入本文中。
術語「烴基」係通用術語,其涵蓋具有全碳主鏈且由碳及氫原
子組成之脂族、脂環族及芳族基團。在某些情形下,如本文所定義,一或多個構成碳主鏈之碳原子可被特定原子或原子團(諸如經由一或多個雜原子N、O及/或S)置換或中斷。烴基之實例包括烷基、環烷基、環烯基、碳環芳基、烯基、炔基、烷基環烷基、環烷基烷基、環烯基烷基、及碳環芳烷基、烷芳基、芳烯基及芳炔基。此等烴基亦可視情況經一或多個如本文所定義之取代基取代。因此,本說明書及申請專利範圍中所論述之化學基團或部分應理解為包括經取代或未經取代之形式。除非上下文另有指示,否則下文所明示之實例及較佳項亦適用於本文所述式之化合物之取代基之各種定義中所提及之各個烴基取代基或含烴基取代基。
較佳的非芳族烴基為飽和基團,諸如烷基及環烷基。一般而言,舉例來說,除非上下文另有要求,否則烴基可具有至多五十個碳原子。以具有1至30個碳原子之烴基較佳。在具有1至30個碳原子之烴基之子集中,特定實例為C1-20烴基,諸如C1-12烴基(例如C1-6烴基或C1-4烴基),具體實例係選自C1至C30烴基之任何個別數值或數值組合。
烷基意欲包括直鏈、分支鏈或環狀烴結構及其組合。低碳數烷基係指具有1至6個碳原子之烷基。低碳數烷基之實例包括甲基、乙基、丙基、異丙基、丁基及第二及第三丁基等。較佳的烷基係彼等具有C30或更少碳者。
烷氧基或烷氧基烷基係指透過氧附接至母體結構之具有1至20個碳原子之直鏈、分支鏈或環狀構型及其組合之基團。實例包括甲氧基、乙氧基、丙氧基、異丙氧基、環丙氧基、環己氧基等。
醯基係指甲醯基及透過羰基官能度附接至母體結構之具有1、2、3、4、5、6、7、8、9、10、11及12個碳原子之直鏈、分支鏈或環狀構型、飽和、不飽和及芳族及其組合之基團。實例包括乙醯基、苯甲醯基、丙醯基、異丁醯基、第三丁氧羰基、苄氧基羰基等。低碳數
醯基係指含一至六個碳之基團。
除非上下文另有指示,否則提及如本文所使用之「碳環」或「環烷基」應包括芳族及非芳族環系統。因此,例如,該術語之範圍包括芳族、非芳族、不飽和、部分飽和及完全飽和碳環系統。一般而言,此等基團可為單環或二環,且可包含(例如)3至12個環組員,更通常5至10個環組員。單環基團之實例為含3、4、5、6、7及8個環組員,更通常3至7個,及較佳5或6個環組員之基團。二環基團之實例為彼等含有8、9、10、11及12個環組員,及更通常9或10個環組員者。非芳族碳環/環烷基之實例包括環丙基、環丁基、環戊基、環己基等。C7至C10多環烴之實例包括諸如降冰片烷及金剛烷基之環系統。
芳基(碳環芳基)係指5-或6-員芳族碳環環;二環9-或10-員芳族環系統;或三環13-或14-員芳族環系統。芳族6-至14-員碳環環包括(例如)經取代或未經取代之苯基、苯、萘、茚滿、萘滿及茀。
經取代之烴基、烷基、芳基、環烷基、烷氧基等係指其中各殘基中至多三個H原子經以下基團取代之具體取代基:烷基、鹵素、鹵代烷基、羥基、烷氧基、羧基、烷氧羰基(亦稱為烷氧基羰基)、甲醯胺基(carboxamido)(亦稱為烷基胺基羰基)、氰基、羰基、硝基、胺基、烷基胺基、二烷基胺基、巰基、烷硫基、亞碸、砜、醯基胺基、甲脒基、苯基、苄基、鹵基苄基、雜芳基、苯氧基、苄氧基、雜芳氧基、苯甲醯基、鹵代苯甲醯基或低碳數烷基羥基。
如上所概述,本發明係關於一種熱及紫外(UV)光穩定組合物,其包含鄰-羥基參-芳基-s-三嗪化合物、受阻胺光穩定劑(HALS)化合物、受阻羥基苯甲酸酯化合物、亞磷酸酯化合物、酸清除劑及受阻酚抗氧化劑化合物。在另一實施例中,該熱及UV光穩定組合物除上述化合物以外亦包含硫酯化合物。
較佳地,該鄰-羥基參-芳基-s-三嗪化合物係式(I)之2-(2’-羥苯
基)-1,3,5-三嗪化合物:
其中式(I)中之R34及R35各獨立地選自視情況經取代之C6-C10芳基、經C1-C10烴基取代之胺基、C1-C10醯基及C1-C10烷氧基;且其中式(I)中在式I之苯氧基部分之位置0至4上之R36係相同或不同,且獨立地選自羥基、C1-C12烴基、C1-C12烷氧基、C1-C12烷氧基酯及C1-C12醯基。
2-(2’-羥苯基)-1,3,5-三嗪之實例包括4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4-辛氧基苯基)-s-三嗪;4,6-雙-(2,4-二甲基苯基)-2-(2,4-二羥苯基)-s-三嗪;2,4-雙(2,4-二羥苯基)-6-(4-氯苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-羥基-乙氧基)苯基]-6-(4-氯苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-羥基-4-(2-羥基-乙氧基)苯基]-6-(2,4-二甲基苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-羥基乙氧基)苯基]-6-(4-溴苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-乙醯氧基乙氧基)苯基]-6-(4-氯苯基)-s-三嗪;2,4-雙(2,4-二羥苯基)-6-(2,4-二甲基苯基)-s-三嗪;2,4-雙(4-聯苯基)-6-[2-羥基-4-[(辛氧基羰基)亞乙基氧基]苯基]-s-三嗪;2,4-雙(4-聯苯基)-6-[2-羥基-4-(2-乙基己氧基)苯基]-s-三嗪;2-苯基-4-[2-羥基-4-(3-第二丁氧基-2-羥基丙氧基)苯基]-6-[2-羥基-4-(3-第二戊氧基-2-羥基丙氧基)苯基]-s-三嗪;2,4-雙(2,4-二甲基苯基)-6-[2-羥基-4(-3-苄氧基-2-羥基丙氧基)苯基]-s-三嗪;2,4-雙(2-羥基-4-正丁氧基苯基)-6-(2,4-二-正丁氧基苯
基)-s-三嗪;2,4-雙(2,4-二甲基苯基)-6-[2-羥基-4-(3-壬氧基-2-羥基丙氧基)-5-α-異丙苯基]-s-三嗪;亞甲基雙-{2,4-雙(2,4-二甲基苯基)-6-[2-羥基-4-(3-丁氧基-2-羥基丙氧基)苯基]-s-三嗪};亞甲基橋聯之二聚體混合物,在位置3:5'、5:5'及3:3'以5:4:1之比例橋接;2,4,6-參(2-羥基-4-異辛氧基羰基亞異丙基氧基-苯基)-s-三嗪;2,4-雙(2,4-二甲基苯基)-6-(2-羥基-4-己氧基-5-α-異丙苯基)-s-三嗪;2-(2,4,6-三甲基苯基)-4,6-雙[2-羥基-4-(3-丁氧基-2-羥基丙氧基)苯基]-s-三嗪;2,4,6-參[2-羥基-4-(3-第二丁氧基-2-羥基丙氧基)-苯基]-s-三嗪;4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4-(3-十二烷氧基-2-羥基丙氧基)苯基)-s-三嗪及4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4-(3-十三烷氧基-2-羥基丙氧基)苯基)-s-三嗪之混合物;4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4(3-(2-乙基己氧基)-2-羥基丙氧基)-苯基)-s-三嗪;4,6-二苯基-2-(4-己氧基-2-羥苯基)-s-三嗪;2-(4,6-二苯基-1,3,5-三嗪-2-基)-5-[2-(2-乙基己醯氧基)乙氧基]苯酚;2,4,6-參(2-羥基-4-辛氧基苯基)-1,3,5-三嗪;丙酸2,2’,2”-[1,3,5-三嗪-2,4,6-三基參[(3-羥基-4,1-伸苯基)氧基]]參-1,1’,1”-三辛基酯;丙酸2-[4-[4,6-雙([1,1’-聯苯]-4-基)-1,3,5-三嗪-2基]-3-羥基苯氧基]-異辛基酯;及其組合。
HALS化合物包括式(II)之分子片段:
其中式(II)中之R31係選自:氫;OH;C1-C20烴基;-CH2CN;C1-C12醯基;及C1-C18烷氧基;式(II)中之R38係選自:氫;及C1-C8烴基;
且式(II)中之R29、R30、R32及R33各獨立地選自C1-C20烴基,或式(II)中之R29及R30及/或R32及R33與附接至其之碳一起形成C5-C10環烷基;或式(IIa)之分子片段
其中式(IIa)中之m係1至2之整數;R39係選自:氫;OH;C1-C20烴基;-CH2CN;C1-C12醯基;及C1-C18烷氧基;且式(IIa)中之G1至G4各獨立地選自C1-C20烴基。
HALS化合物之實例包括癸二酸雙(2,2,6,6-四甲基哌啶-4-基)酯;琥珀酸雙(2,2,6,6-四甲基哌啶-4-基)酯;癸二酸雙(1,2,2,6,6-五甲基哌啶-4-基)酯;癸二酸雙(1-辛氧基-2,2,6,6-四甲基哌啶-4-基)酯;3,5-二-第三丁基-4-羥基苄基丙二酸雙(1,2,2,6,6-五甲基哌啶-4-基)正丁基酯;1-(2-羥乙基)-2,2,6,6-四甲基-4-羥基哌啶及琥珀酸之縮合物;2,2,6,6-四甲基哌啶-4-基硬脂酸酯;十二烷酸2,2,6,6-四甲基哌啶-4-基酯;硬脂酸1,2,2,6,6-五甲基哌啶-4-基酯;十二烷酸1,2,2,6,6-五甲基哌啶-4-基酯;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-第三辛基胺基-2,6-二氯-1,3,5-三嗪之縮合物;次氮基三乙酸參(2,2,6,6-四甲基哌啶-4-基)酯;肆(2,2,6,6-四甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;4-苯甲醯基-2,2,6,6-四甲基哌啶;4-硬脂基氧基-2,2,6,6-四甲基哌啶;雙(1,2,2,6,6-五甲基哌啶基)-2-正丁基-2-(2-羥基-3,5-二-第三丁基苄基)丙二酸酯;3-正辛基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸-2,4-二酮;
癸二酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;琥珀酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-嗎啉基-2,6-二氯-1,3,5-三嗪之縮合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及甲基化4-嗎啉基-2,6-二氯-1,3,5-三嗪之縮合物;2-氯-4,6-雙(4-正丁基胺基-2,2,6,6-四甲基哌啶基)-1,3,5-三嗪及1,2-雙(3-胺基丙胺基)乙烷之縮合物;2-氯-4,6-雙(4-正丁基胺基-1,2,2,6,6-五甲基哌啶基)-1,3,5-三嗪及1,2-雙-(3-胺基丙胺基)乙烷之縮合物;8-乙醯基-3-十二烷基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸烷-2,4-二酮;3-十二烷基-1-(2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1-乙醯基-2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1,2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;4-十六烷氧基-2,2,6,6-四甲基哌啶及4-硬脂基氧基-2,2,6,6-四甲基哌啶之混合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-環己基胺基-2,6-二氯-1,3,5-三嗪之縮合物;1,2-雙(3-胺基丙胺基)乙烷、2,4,6-三氯-1,3,5-三嗪及4-丁基胺基-2,2,6,6-四甲基哌啶之縮合物;2-十一烷基-7,7,9,9-四甲基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷;側氧基-哌嗪基-三嗪;7,7,9,9-四甲基-2-環十一烷基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷及表氯醇之反應產物;肆(2,2,6,6-四甲基-4-哌啶基)丁烷-1,2,3,4-四羧酸酯;1,2,3,4-丁烷四羧酸肆(1,2,2,6,6-五甲基-4-哌啶基)酯;1,2,3,4-丁烷四羧酸1,2,2,6,6-五甲基-4-哌啶基十三烷基酯;1,2,3,4-丁烷四羧酸2,2,6,6-四甲基-4-哌啶基十三烷基酯;1,2,3,4-丁烷四羧酸與2,2,6,6-四甲基-2,4,8,10-四氧雜螺[5.5]-十一烷-3,9-二乙醇1,2,2,6,6-五甲基-4-哌啶基酯之聚合物;1,2,3,4-丁烷四羧酸與2,2,6,6-四甲基-2,4,8,10-四氧雜螺[5.5]-十一烷-3,9-二乙醇2,2,6,6-四甲基-4-哌啶基酯之聚合物;雙(1-十一烷氧基-2,2,6,6-四甲基哌啶-4-基)碳酸酯;1-(2-羥基-2-甲基丙氧基)-2,2,6,6-四甲基-4-哌啶酚;1-(2-羥基-2-
甲基丙氧基)-4-十八醯氧基-2,2,6,6-四甲基哌啶;1-(4-十八醯氧基-2,2,6,6-四甲基哌啶-1-基氧基)-2-十八醯氧基-2-甲基丙烷;1-(2-羥乙基)-2,2,6,6-四甲基-4-哌啶酚;1-(2-羥乙基)-2,2,6,6-四甲基-4-哌啶酚及二甲基琥珀酸酯之反應產物;2,2,4,4-四甲基-7-氧雜-3,20-二氮雜二螺[5.1.11.2]二十一烷-21-酮;2,2,6,6-四甲基-4-哌啶酚與高級脂肪酸之酯;3-十二烷基-1-(2,2,6,6-四甲基-4-哌啶基)吡咯啶-2,5-二酮;1-十八烷基-1H-吡咯-2,5-二酮與(1-甲基乙烯基)苯及1-(2,2,6,6-四甲基-4-哌啶基)-1H-吡咯-2,5-二酮之聚合物;哌嗪酮,1,1',1"-[1,3,5-三嗪-2,4,6-三基參[(環己基亞胺基)-2,1-乙二基]]參[3,3,5,5-四甲基-;哌嗪酮,1,1',1"-[1,3,5-三嗪-2,4,6-三基參[(環己基亞胺基)-2,1-乙二基]]參[3,3,4,5,5-五甲基-;7,7,9,9-四甲基-2-環十一烷基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷及表氯醇之反應產物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-環己基胺基-2,6-二氯-1,3,5-三嗪之縮合物;1,2-雙(3-胺基丙胺基)乙烷、2,4,6-三氯-1,3,5-三嗪及4-丁基胺基-2,2,6,6-四甲基哌啶之縮合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-嗎啉基-2,6-二氯-1,3,5-三嗪之縮合物;2-氯-4,6-雙(4-正丁基胺基-2,2,6,6-四甲基哌啶基)-1,3,5-三嗪及1,2-雙(3-胺基丙胺基)乙烷之縮合物;2-氯-4,6-雙(4-正丁基胺基-1,2,2,6,6-五甲基哌啶基)-1,3,5-三嗪及1,2-雙-(3-胺基丙胺基)乙烷之縮合物;2-[(2-羥乙基)胺基]-4,6-雙[N-(1-環己氧基-2,2,6,6-四甲基哌啶-4-基)丁基胺基-1,3,5-三嗪;丙烷二酸[(4-甲氧基苯基)-亞甲基]-雙-(1,2,2,6,6-五甲基-4-哌啶基)酯;肆(2,2,6,6-四甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;3,5-雙(1,1-二甲基乙基)-4-羥基-苯丙酸1-[2-[3-[3,5-雙(1,1-二甲基乙基)-4-羥苯基]-1-側氧基丙氧基]乙基]-2,2,6,6-四甲基-4-哌啶基酯;N-(1-辛氧基-2,2,6,6-四甲基哌啶-4-基)-N'-十二烷基草醯胺;次氮基三乙酸參(2,2,6,6-四甲基哌啶-4-基)酯;1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,
雙(1,2,2,6,6-五甲基-4-哌啶基):1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(2,2,6,6-四甲基-4-哌啶基);1-(2-羥乙基)-2,2,6,6-四甲基-4-羥基哌啶及琥珀酸之縮合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-第三辛基胺基-2,6-二氯-1,3,5-三嗪之縮合物;1,2,3,4-丁烷四羧酸1,2,2,6,6-五甲基-4-哌啶基十三烷基酯;肆(2,2,6,6-四甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;1,2,3,4-丁烷四羧酸2,2,6,6-四甲基-4-哌啶基十三烷基酯;肆(1,2,2,6,6-五甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;2,2,4,4-四甲基-21-側氧基-7-氧雜-3.20-二氮雜螺(5.1.11.2)-二十一烷-20-丙酸-十二烷基酯及2,2,4,4-四甲基-21-側氧基-7-氧雜-3.20-二氮雜螺(5.1.11.2)-二十一烷-20-丙酸-十四烷基酯之混合物;1H,4H,5H,8H-2,3a,4a,6,7a,8a-六氮雜環戊烷并[def]茀-4,8-二酮,六氫-2,6-雙(2,2,6,6-四甲基-4-哌啶基)-;聚甲基[丙基-3-氧基(2',2',6',6'-四甲基-4,4'-哌啶基)]矽氧烷;聚甲基[丙基-3-氧基(1',2',2',6',6'-五甲基-4,4'-哌啶基)]矽氧烷;甲基丙烯酸甲酯與丙烯酸乙酯及丙烯酸2,2,6,6-四甲基哌啶-4-基酯之共聚物;混合C20至C24 α-烯烴與(2,2,6,6-四甲基哌啶-4-基)琥珀醯亞胺之共聚物;1,2,3,4-丁烷四羧酸與β,β,β',β'-四甲基-2,4,8,10-四氧雜螺[5.5]十一烷-3,9-二乙醇1,2,2,6,6-五甲基-4-哌啶基酯之聚合物;1,2,3,4-丁烷四羧酸與β,β,β',β'-四甲基-2,4,8,10-四氧雜螺[5.5]十一烷-3,9-二乙醇2,2,6,6-四甲基-4-哌啶基酯共聚物之聚合物;N,N'-雙(2,2,6,6-四甲基-4-哌啶基)-1,3-苯二羧醯胺;1,1'-(1,10-二側氧基-1,10-癸二基)-雙(六氫-2,2,4,4,6-五甲基嘧啶;N-(1-乙醯基-2,2,6,6-四甲基哌啶基)-N'-十二烷基乙二醯胺;N,N'-1,6-己二基雙[N-(2,2,6,6-四甲基-4-哌啶基)-甲醯胺;1,3:2,4-雙-O-(2,2,6,6-四甲基-4-伸哌啶基)-D-葡萄糖醇;2,2,4,4-四甲基-7-氧雜-3,20-二氮雜-21-側氧基-二螺[5.1.11.2]二十一烷;2-甲基-N-(2,2,6,6-四甲基-4-哌啶基)-2-[(2,2,6,6-四甲基-4-哌啶基)胺基]-丙醯胺;2,2,4,4-四甲基-21-側氧基-
7-氧雜-3,20-二氮雜二螺[5.1.11.2]二十一烷-20-丙酸十二烷基酯;N-(2,2,6,6-四甲基哌啶-4-基)-β-胺基丙酸十二烷基酯;N-(2,2,6,6-四甲基哌啶-4-基)-N'-胺基草醯胺;N-(2,2,6,6-四甲基-4-哌啶基)-3-[(2,2,6,6-四甲基-4-哌啶基)胺基]-丙醯胺;4-十六烷氧基-2,2,6,6-四甲基哌啶及4-硬脂基氧基-2,2,6,6-四甲基哌啶之混合物;3-十二烷基-1-(1,2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1-乙醯基-2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;琥珀酸雙(2,2,6,6-四甲基哌啶-4-基)酯;3,5-二-第三丁基-4-羥基苄基丙二酸雙(1,2,2,6,6-五甲基哌啶-4-基)正丁基酯;次氮基三乙酸參(2,2,6,6-四甲基哌啶-4-基)酯;1,1'-(1,2-乙二基)雙(3,3,5,5-四甲基哌嗪酮);4-苯甲醯基-2,2,6,6-四甲基哌啶;4-硬脂基氧基-2,2,6,6-四甲基哌啶;雙(1,2,2,6,6-五甲基哌啶基)-2-正丁基-2-(2-羥基-3,5-二-第三丁基苄基)丙二酸酯;3-正辛基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸-2,4-二酮;癸二酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;琥珀酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;8-乙醯基-3-十二烷基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸烷-2,4-二酮;3-十二烷基-1-(2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1-乙醯基-2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1,2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;4-十六烷氧基-2,2,6,6-四甲基哌啶及4-硬脂基氧基-2,2,6,6-四甲基哌啶之混合物;2-十一烷基-7,7,9,9-四甲基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷;1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(2,2,6,6-四甲基-4-哌啶基)及1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(1,2,2,6,6-五甲基-4-哌啶基);N1-(β-羥乙基)3,3-五亞甲基-5,5-二甲基哌嗪-2-酮;N1-第三辛基-3,3,5,5-四甲基-二氮呯-2-酮;N1-第三辛基-3,3-五亞甲基-5,5-六亞甲基-二氮呯-2-酮;N1-第三辛基-3,3-五亞甲基-5,5-二甲基哌嗪-2-酮;反式-1,2-環己烷-雙-(N1-5,5-二甲基-3,3-五亞甲基-2-哌嗪酮;反
式-1,2-環己烷-雙-(N1-3,3,5,5-二螺五亞甲基-2-哌嗪酮);N1-異丙基-1,4-二氮雜二螺-(3,3,5,5)五亞甲基-2-哌嗪酮;N1-異丙基-1,4-二氮雜二螺-3,3-五亞甲基-5,5-四亞甲基-2-哌嗪酮;N1-異丙基-5,5-二甲基-3,3-五亞甲基-2-哌嗪酮;反式-1,2-環己烷-雙-N1-(二甲基-3,3-五亞甲基-2-哌嗪酮);N1-辛基-5,5-二甲基-3,3-五亞甲基-1,4-二氮呼-2-酮;N1-辛基-1,4-二氮雜二螺-(3,3,5,5)五亞甲基-1,5-二氮呼-2-酮;及其混合物。
該受阻羥基苯甲酸酯化合物係式(III)化合物:
其中式(III)中之R17係C1-C8烷基,且式(III)中之R18係C1-C24烷基或經取代或未經取代之C6-C24芳基。特定言之,該受阻羥基苯甲酸酯化合物係3,5-二-第三丁基-4-羥基苯甲酸2,4-二-第三丁基苯基酯;3,5-二-第三丁基-4-羥基苯甲酸十六烷基酯;3,5-二-第三丁基-4-羥基苯甲酸十八烷基酯;3,5-二-第三丁基-4-羥基苯甲酸辛酯;3,5-二-第三丁基-4-羥基苯甲酸十四烷基酯;3,5-二-第三丁基-4-羥基苯甲酸山萮酯;3,5-二-第三丁基-4-羥基苯甲酸2-甲基-4,6-二-第三丁基苯基酯或3-[3-第三丁基-4-(3,5-二-第三丁基-4-羥基苯甲醯氧基)苯基]丙酸丁酯。
用於熱及UV光穩定組合物之酸清除劑可包括以下化合物中之一或多者:氧化鋅、乳酸鈣、天然及合成水滑石、天然及合成水鋁鈣石、高級脂肪酸之鹼金屬鹽及鹼土金屬鹽、硬脂酸鈣、硬脂酸鋅、山
萮酸鎂、硬脂酸鎂、硬脂酸鈉、蓖麻油酸鈉及棕櫚酸鉀、鄰苯二酚酸銻、鄰苯二酚酸鋅。在一實例中,該酸清除劑包括氧化鎂、氧化鋁、氫氧化鎂、氫氧化鋁、其碳酸鹽或其混合物。酸清除劑之具體實例包括DHT-4A(CAS No.11097-59-9),一種氫氧化碳酸鋁鎂水合物,其係合成水滑石化合物。
該受阻酚抗氧化劑化合物包括式(IVa)、(IVb)或(IVc)中一或多者之分子片段:
其中式(IVa)、(IVb)及(IVc)中之R18係選自氫及C1-4烴基;式(IVa)、(IVb)及(IVc)中之R19及R20各選自氫及C1-C20烴基;且式(IVa)、(IVb)及(IVc)中之R37係選自C1-C12烴基。在一實施例中,式(IVa)、(IVb)及(IVc)中之R18及R37係選自甲基及第三丁基。該受阻酚抗氧化劑化合物之實例包括(1,3,5-參(4-第三丁基-3-羥基-2,6-二甲基苄基)-1,3,5-三嗪-2,4,6-(1H,3H,5H)-三酮;1,3,5-參(3,5-二-第三丁基-4-羥基苄基)-1,3,5-三嗪-2,4,6(1H,3H,5H)-三酮;1,1,3-參(2’-甲基-4’-羥基-5’-第三丁基苯基)丁烷;三乙二醇雙[3-(3-第三丁基-4-羥基-5-甲基苯基)丙酸酯];4,4’-硫基雙(2-第三丁基-5-甲基酚);2,2’-硫基二伸乙基雙[3-(3-第三丁基-4-羥基-5-甲基苯基)丙酸酯];3-(3’-第三丁基-4’-羥基-5’-甲基苯基)丙酸十八烷基酯;肆亞甲基(3-第三丁基-4-羥基-5-甲基氫化肉桂酸酯)甲烷;N,N’-六亞甲基雙[3-(3-第三丁基-4-羥基-5-甲基苯基)丙醯胺];硫代二丙酸二(4-第三丁基-3-羥基-2,6-二甲基苄基
酯);及3,5-二-(第三)丁基-4-羥基氫化肉桂酸十八烷基酯。
用於該熱及UV光穩定組合物中之亞磷酸酯可為受阻亞磷酸芳烷基酯或亞磷酸三芳基酯或其混合物。該受阻亞磷酸芳烷基酯係式(V)化合物:
其中式(V)中之R1、R2、R3、R4、R5、R6、R7、R8、R9及R10各個別地選自氫、C1-C12烷基、C3-C12環烷基、C4-C12烷基環烷基、C6-C10芳基及C7-C12烷芳基,其中R1及R5總共包含至少5個碳,且R1及R5中之至少一者包含三級碳,其中R6及R10總共包含至少5個碳,且R6及R10中之至少一者包含三級碳。該受阻亞磷酸芳烷基酯之實例包括:雙-(2,6-二-第三丁基-4-甲基苯基)季戊四醇二亞磷酸酯、(雙-(2,4-二異丙苯基)季戊四醇二亞磷酸酯、雙-(2,4-二-第三丁基-苯基)季戊四醇二亞磷酸酯及雙-(2,4,6-三-第三丁基-苯基)季戊四醇二磷酸酯。
該亞磷酸三芳基酯係式(VI)化合物:
其中式(VI)中之R16、R17、R40、R41及R42各個別地選自氫、C1-C20烷基、C3-C20環烷基、C4-C20烷基環烷基、C6-C10芳基及C7-C20烷芳基。該亞磷酸三芳基酯之實例包括:亞磷酸參-(2,4-二-第三丁基苯基)
酯、亞磷酸參(4-壬基苯基)酯及亞磷酸三苯基酯。
該硫酯化合物係硫代二丙酸二月桂基酯、硫代二丙酸二硬脂基酯、季戊四醇肆-(3-十二烷基硫代丙酸酯)、硫乙基硫代二琥珀酸四烷基酯、2,12-二羥基-4,10-二硫雜-7-氧雜十三亞甲基雙[3-(十二烷硫基)丙酸酯]、烷硫基-鏈烷酸之聚烷醇酯或3,3'-硫代二丙酸二烷基酯。
在該熱及UV光穩定組合物之一調配物中,該組合物包含介於約1.00重量%至約10.00重量%(較佳約2.00重量%至約6.00重量%)內之鄰-羥基參-芳基-s-三嗪化合物、介於約20.00重量%至約50.00重量%(較佳約25.00重量%至約35.00重量%)內之受阻胺光穩定劑化合物、介於約20.00重量%至約50.00重量%(較佳約25.00重量%至約35.00重量%)內之受阻羥基苯甲酸酯化合物、介於1重量%至約10重量%(較佳約2.0重量%至約8.0重量%)內之酸清除劑、介於約1重量%至約10重量%(較佳約2.00重量%至約6.00重量%)內之受阻酚抗氧化劑化合物及介於約5.00重量%至約40.00重量%(較佳約20.00重量%至約30.00重量%)內之亞磷酸酯化合物,其中各組分之重量%係基於該熱及UV光穩定組合物之總重量。
在另一實施例中,該熱及UV光穩定組合物之調配物包含介於約1.00重量%至約10.00重量%(較佳約2.00重量%至約6.00重量%)內之鄰-羥基參-芳基-s-三嗪化合物、介於約20.00重量%至約50.00重量%(較佳約30.00重量%至約40.00重量%)內之受阻胺光穩定劑化合物、介於約20.00重量%至約50.00重量%(較佳約30.00重量%至約40.00重量%)內之受阻羥基苯甲酸酯化合物、介於1重量%至約10重量%(較佳約2.00重量%至約8.00重量%)內之酸清除劑、介於約1重量%至約10重量%(較佳約2.00重量%至約6.00重量%)內之受阻酚抗氧化劑化合物、介於約5.00重量%至約25.00重量%(較佳約6.00重量%至約12.00重量%)內之亞磷酸酯化合物及介於約1.00重量%至約15.00重量%(較佳約5.00
重量%至10.00重量%)內之硫酯化合物,其中各組分之重量%係基於該熱及UV光穩定組合物之總重量。
在一特定實施例中,該熱及UV光穩定組合物之調配物包含約4重量%之鄰-羥基參-芳基-s-三嗪化合物、約34重量%之受阻胺光穩定劑化合物、約34重量%之受阻羥基苯甲酸酯化合物、約7重量%之酸清除劑、約4重量%之受阻酚抗氧化劑化合物、約10重量%之亞磷酸酯化合物及約7重量%之硫酯化合物,其中各組分之重量%係基於該熱及UV光穩定組合物之總重量。
在另一特別實施例中,該熱及UV光穩定組合物之調配物包含約4重量%之鄰-羥基參-芳基-s-三嗪化合物、約30重量%之受阻胺光穩定劑化合物、約30重量%之受阻羥基苯甲酸酯化合物、約7重量%之酸清除劑、約4重量%之受阻酚抗氧化劑化合物及約25重量%之亞磷酸酯化合物,其中各組分之重量%係基於該熱及UV光穩定組合物之總重量。
該熱及UV光穩定組合物可以此項技術中已知之任何方式與待穩定物質(例如,聚合物)組合在一起,從而形成屬於穩定物質之組合物(本文亦稱為穩定組合物或組合物)。可與熱及UV光穩定組合物組合之待穩定之物質包括(但不限於)聚合物,諸如聚烯烴、聚酯、聚醚、聚酮、聚醯胺、天然及合成橡膠、聚胺基甲酸酯、聚苯乙烯、耐衝擊聚苯乙烯、聚丙烯酸酯、聚甲基丙烯酸酯、聚縮醛、聚丙烯腈、聚丁二烯、聚苯乙烯、丙烯腈-丁二烯-苯乙烯、苯乙烯丙烯腈、丙烯酸酯苯乙烯丙烯腈、乙酸丁酸纖維素、纖維素聚合物、聚醯亞胺、聚醯胺醯亞胺、聚醚醯亞胺、聚苯硫醚、聚苯醚聚碸、聚醚碸、聚氯乙烯、聚碳酸酯、聚酮、脂族聚酮、熱塑性烯烴、胺基樹脂交聯聚丙烯酸酯及聚酯、聚異氰酸酯交聯聚酯及聚丙烯酸酯、苯酚/甲醛、脲/甲醛及三聚氰胺/甲醛樹脂、乾燥及非乾燥醇酸樹脂、醇酸樹脂、聚酯樹脂、
與三聚氰胺樹脂、尿素樹脂、異氰酸酯、異氰尿酸酯、胺基甲酸酯及環氧樹脂交聯之丙烯酸酯樹脂、衍生自脂族、環脂族、雜環及芳族縮水甘油基化合物(其與酐或胺交聯)之交聯環氧樹脂、聚矽氧烷、邁克爾加成聚合物、胺、具有活性不飽和及亞甲基化合物之封端胺、具有活性不飽和及亞甲基化合物之酮亞胺、與不飽和丙烯酸聚乙醯乙酸酯樹脂組合之聚酮亞胺、與不飽和丙烯酸樹脂組合之聚酮亞胺、輻射可固化組合物、環氧三聚氰胺樹脂、及有機染料、化妝品、纖維素基紙調配物、照相軟片紙、纖維、蠟、油墨及其摻合物。
較佳地,該待穩定之物質係聚合物,諸如熱塑性烯烴、丙烯腈-丁二烯-苯乙烯、聚酯、聚氯乙烯、聚醯胺、聚胺基甲酸酯或丙烯、異丁烯、丁烯、甲基戊烯、己烯、庚烯、辛烯、異戊二烯、丁二烯、己二烯、二環戊烷二烯、亞乙基、環戊烯及降冰片烯之均聚物及共聚物。更佳地,該待穩定之物質係聚丙烯及熱塑性烯烴。
在一實施例中,預期該待穩定之物質可為用於建造或翻修建築(例如,房屋、辦公室、倉庫等)之物質或物品。例如,該待穩定之物質可包括乙烯基擋板、乙烯基擋板邊飾、百葉窗、山墻通風口、屋簷、招牌、拱腹、模具、屋頂瓦、屋頂襯底或底板、屋頂膜、板條系統、板條延伸件、防水板、瓦盤、屋脊通風口、露天磚、屋脊系統(亦稱為屋脊瓦)、屋簷立管、錐形帶、山墻端楔形物、傾斜邊飾、防滲膜、複合甲板材料、欄杆、窗框及其他用於建造或翻修建築之物質及物品。
在一實施例中,將該待穩定之物質及熱及UV光穩定組合物組合形成「母料」組合物。在一實施例中,基於該母料組合物之總重量計,該母料組合物包含介於10重量%至約80重量%內之熱及UV光穩定化合物,且剩餘者為該待穩定之物質。在一更佳實施例中,基於該母料組合物之總重量計,該母料組合物包含介於30重量%至約60重量%
內之熱及UV光穩定組合物,且剩餘者為該待穩定之物質。在另一實施例中,基於該母料組合物之總重量計,該母料組合物包含介於40重量%至約50重量%內之熱及UV光穩定組合物,且剩餘者為該待穩定之物質。
一實施例包括母料濃縮物,其包含如本文所述實施例中任一項之穩定組合物及至少一種與待穩定之物質相同或相容之有機物質,其中該穩定物質基於該母料濃縮物之總重量計係以10重量%至90重量%之量存在。
在某些實施例中,基於該待穩定之物質之總重量計,終端穩定組合物中之如本文所述熱及UV穩定組合物之存在量係於0.01重量%至5重量%之範圍內之任一點。在一特定實施例中,基於該待穩定之物質之總重量計,終端穩定組合物中之熱及UV穩定組合物之存在量係於0.05重量%至2重量%之範圍內之任一點。
如本文所述熱及UV穩定組合物之具體組分可以各種量存在於穩定組合物中,端視該待穩定之物質及/或所需保護水平而定。例如,基於穩定組合物之總重量計,終端穩定組合物中之鄰-羥基參-芳基-s-三嗪化合物之量可介於約0.002重量%至約0.50重量%,較佳0.004重量%至約0.20重量%,更佳0.005重量%至約0.1重量%之範圍內。
基於該穩定組合物之總重量計,該穩定組合物中之受阻胺光穩定劑化合物之量係約0.01重量%至約1.20重量%,較佳約0.02重量%至約0.80重量%,更佳0.03重量%至約0.62重量%。
基於該穩定組合物之總重量計,該穩定組合物中之受阻羥基苯甲酸酯化合物之量係約0.01重量%至約1.20重量%,較佳約0.02重量%至約0.80重量%,更佳約0.03重量%至約0.62重量%。
基於該穩定組合物之總重量計,該穩定組合物中之酸清除劑之量係約0.001重量%至約0.50重量%,較佳約0.003重量%至約0.25重量
%,更佳0.006重量%至約0.14重量%。
基於該穩定組合物之總重量計,該穩定組合物中之受阻酚抗氧化劑化合物之量係約0.001重量%至約0.50重量%,較佳約0.002重量%至約0.25重量%,更佳約0.004重量%至約0.085重量%。
基於該穩定組合物之總重量計,該穩定組合物中之亞磷酸酯化合物之量係約0.005重量%至約1.00重量%,較佳約0.01重量%至約0.80重量%,更佳約0.02重量%至約0.5重量%。
基於該穩定組合物之總重量計,該穩定組合物中之硫酯化合物之量係約0.001重量%至約0.80重量%,較佳約0.003重量%至約0.4重量%,更佳約0.006重量%至約0.2重量%。
本申請案亦涵蓋一種藉由將熱及UV光穩定組合物與待穩定之物質組合在一起製備上述組合物之方法。術語「組合」或「經組合」意欲包括可組合熱及UV光穩定組合物之所有方式,且包括(例如,相互混合(intermixing)、混合(admixing)、整合、混合(mixing)、摻合等)。此外,注意,熱及UV光穩定組合物及待穩定之物質可以任何次序組合,亦即,可將熱及UV光穩定組合物添加至待穩定之物質,或反之亦然,或可將熱及UV光穩定組合物及待穩定之物質同時添加至容器。
待穩定之物質及熱及UV光穩定組合物可藉由在捏合裝置(諸如,單或雙螺桿擠出機、班伯里(Banbury)混煉機或熱軋輥)中摻合或混合(compounding)組分而組合。此等捏合裝置之加工參數及用法係熟習此項技術者所熟知。
熟習製造塑膠材料技術者將知曉,除待穩定之物質及熱及UV光穩定組合物意外,本發明組合物亦可包含習知添加劑,包括(但不限於)金屬鈍化劑、硝銅、內酯、共穩定劑、成核劑、澄清劑、中和劑、金屬硬脂酸鹽、金屬氧化物、水滑石、填充劑及強化劑、增塑
劑、潤滑劑、乳化劑、顏料、流變添加劑、觸媒、調平劑(level agent)、光學增亮劑、阻燃劑、防靜電劑及發泡劑。
本發明包括至少以下實施例:
實施例1
一種熱及紫外(UV)光穩定組合物,其包含:鄰-羥基參-芳基-s-三嗪化合物;受阻胺光穩定劑化合物;受阻羥基苯甲酸酯化合物;酸清除劑;亞磷酸酯化合物;及受阻酚抗氧化劑化合物。
實施例2
如實施例1之熱及UV光穩定組合物,其另外包含硫酯化合物。
實施例3
如前述實施例中任一項之熱及UV光穩定組合物,其中該鄰-羥基參-芳基-s-三嗪化合物係式(I)之2-(2’-羥苯基)-1,3,5-三嗪化合物:
其中式(I)中之R34及R35各獨立地選自視情況經取代之C6-C10芳基、經C1-C10烴基-取代之胺基、C1-C10醯基及C1-C10烷氧基;且其中式(I)中在式I之苯氧基部分之位置0至4上之R36係相同或不同,且獨立地選自羥基、C1-C12烴基、C1-C12烷氧基、C1-C12烷氧基酯及C1-C12醯
基。
實施例4
如實施例3之熱及UV光穩定組合物,其中該2-(2’-羥苯基)-1,3,5-三嗪化合物係選自:4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4-辛氧基苯基)-s-三嗪;4,6-雙-(2,4-二甲基苯基)-2-(2,4-二羥苯基)-s-三嗪;2,4-雙(2,4-二羥苯基)-6-(4-氯苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-羥基-乙氧基)苯基]-6-(4-氯苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-羥基-4-(2-羥基-乙氧基)苯基]-6-(2,4-二甲基苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-羥基乙氧基)苯基]-6-(4-溴苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-乙醯氧基乙氧基)苯基]-6-(4-氯苯基)-s-三嗪;2,4-雙(2,4-二羥苯基)-6-(2,4-二甲基苯基)-s-三嗪;2,4-雙(4-聯苯基)-6-[2-羥基-4-[(辛氧基羰基)亞乙基氧基]苯基]-s-三嗪;2,4-雙(4-聯苯基)-6-[2-羥基-4-(2-乙基己氧基)苯基]-s-三嗪;2-苯基-4-[2-羥基-4-(3-第二丁氧基-2-羥基丙氧基)苯基]-6-[2-羥基-4-(3-第二戊氧基-2-羥基丙氧基)苯基]-s-三嗪;2,4-雙(2,4-二甲基苯基)-6-[2-羥基-4(-3-苄氧基-2-羥基丙氧基)苯基]-s-三嗪;2,4-雙(2-羥基-4-正丁氧基苯基)-6-(2,4-二-正丁氧基苯基)-s-三嗪;2,4-雙(2,4-二甲基苯基)-6-[2-羥基-4-(3-壬氧基-2-羥基丙氧基)-5-α-異丙苯基]-s-三嗪;亞甲基雙-{2,4-雙(2,4-二甲基苯基)-6-[2-羥基-4-(3-丁氧基-2-羥基丙氧基)苯基]-s-三嗪};亞甲基橋聯之二聚體混合物,在位置3:5'、5:5'及3:3'以5:4:1之比例橋接;2,4,6-參(2-羥基-4-異辛氧基羰基亞異丙基氧基-苯基)-s-三嗪;2,4-雙(2,4-二甲基苯基)-6-(2-羥基-4-己氧基-5-α-異丙苯基)-s-三嗪;2-(2,4,6-三甲基苯基)-4,6-雙[2-羥基-4-(3-丁氧基-2-羥基丙氧基)苯基]-s-三嗪;2,4,6-參[2-羥基-4-(3-第二丁氧基-2-羥基丙氧基)-苯基]-s-三嗪;4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4-(3-十二烷氧基-2-羥基丙氧基)苯基)-s-三嗪及4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4-(3-十三烷氧基-2-羥基丙氧基)苯基)-s-三嗪之混合物;4,6-雙-
(2,4-二甲基苯基)-2-(2-羥基-4(3-(2-乙基己氧基)-2-羥基丙氧基)-苯基)-s-三嗪;4,6-二苯基-2-(4-己氧基-2-羥苯基)-s-三嗪;2-(4,6-二苯基-1,3,5-三嗪-2-基)-5-[2-(2-乙基己醯氧基)乙氧基]苯酚;2,4,6-參(2-羥基-4-辛氧基苯基)-1,3,5-三嗪;丙酸2,2’,2”-[1,3,5-三嗪-2,4,6-三基參[(3-羥基-4,1-伸苯基)氧基]]參-1,1’,1”-三辛基酯;丙酸2-[4-[4,6-雙([1,1’-聯苯]-4-基)-1,3,5-三嗪-2基]-3-羥基苯氧基]-異辛基酯;及其組合。
實施例5
如前述實施例中任一項之熱及UV光穩定組合物,其中該受阻胺光穩定劑化合物包含式(II)之分子片段:
其中式(II)中之R31係選自:氫;OH;C1-C20烴基;-CH2CN;C1-C12醯基;及C1-C18烷氧基;式(II)中之R38係選自:氫;及C1-C8烴基;且式(II)中之R29、R30、R32及R33各獨立地選自C1-C20烴基,或式(II)中之R29及R30及/或R32及R33與附接至其之碳一起形成C5-C10環烷基;式(IIa)之分子片段
式(IIa)
其中式(IIa)中之m係1至2之整數;式(IIa)中之R39係選自:氫;OH;C1-C20烴基;-CH2CN;C1-C12醯基;及C1-C18烷氧基;且式(IIa)中之G1-G4各獨立地選自C1-C20烴基。
實施例6
如前述實施例中任一項之熱及UV光穩定組合物,其中該受阻胺光穩定劑係選自:癸二酸雙(2,2,6,6-四甲基哌啶-4-基)酯;琥珀酸雙(2,2,6,6-四甲基哌啶-4-基)酯;癸二酸雙(1,2,2,6,6-五甲基哌啶-4-基)酯;癸二酸雙(1-辛氧基-2,2,6,6-四甲基哌啶-4-基)酯;3,5-二-第三丁基-4-羥基苄基丙二酸雙(1,2,2,6,6-五甲基哌啶-4-基)正丁基酯;1-(2-羥乙基)-2,2,6,6-四甲基-4-羥基哌啶及琥珀酸之縮合物;硬脂酸2,2,6,6-四甲基哌啶-4-基酯;十二烷酸2,2,6,6-四甲基哌啶-4-基酯;硬脂酸1,2,2,6,6-五甲基哌啶-4-基酯;十二烷酸1,2,2,6,6-五甲基哌啶-4-基酯;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-第三辛基胺基-2,6-二氯-1,3,5-三嗪之縮合物;次氮基三乙酸參(2,2,6,6-四甲基哌啶-4-基)酯;肆(2,2,6,6-四甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;4-苯甲醯基-2,2,6,6-四甲基哌啶;4-硬脂基氧基-2,2,6,6-四甲基哌啶;雙(1,2,2,6,6-五甲基哌啶基)-2-正丁基-2-(2-羥基-3,5-二-第三丁基苄基)丙二酸酯;3-正辛基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸-2,4-二酮;癸二酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;琥珀酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-嗎啉基-2,6-二氯-1,3,5-三嗪之縮合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及甲基化4-嗎啉基-2,6-二氯-1,3,5-三嗪之縮合物;2-氯-4,6-雙(4-正丁基胺基-2,2,6,6-四甲基哌啶基)-1,3,5-三嗪及1,2-雙(3-胺基丙胺基)乙烷之縮合物;2-氯-4,6-雙(4-正丁基胺基-1,2,2,6,6-五甲基哌啶基)-1,3,5-三嗪及1,2-雙-(3-胺基丙胺基)乙烷之縮
合物;8-乙醯基-3-十二烷基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸烷-2,4-二酮;3-十二烷基-1-(2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1-乙醯基-2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1,2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;4-十六烷氧基-2,2,6,6-四甲基哌啶及4-硬脂基氧基-2,2,6,6-四甲基哌啶之混合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-環己基胺基-2,6-二氯-1,3,5-三嗪之縮合物;1,2-雙(3-胺基丙胺基)乙烷、2,4,6-三氯-1,3,5-三嗪及4-丁基胺基-2,2,6,6-四甲基哌啶之縮合物;2-十一烷基-7,7,9,9-四甲基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷;側氧基-哌嗪基-三嗪;7,7,9,9-四甲基-2-環十一烷基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷及表氯醇之反應產物;肆(2,2,6,6-四甲基-4-哌啶基)丁烷-1,2,3,4-四羧酸酯;1,2,3,4-丁烷四羧酸肆(1,2,2,6,6-五甲基-4-哌啶基)酯;1,2,3,4-丁烷四羧酸1,2,2,6,6-五甲基-4-哌啶基十三烷基酯;1,2,3,4-丁烷四羧酸2,2,6,6-四甲基-4-哌啶基十三烷基酯;1,2,3,4-丁烷四羧酸與2,2,6,6-四甲基-2,4,8,10-四氧雜螺[5.5]-十一烷-3,9-二乙醇1,2,2,6,6-五甲基-4-哌啶基酯之聚合物;1,2,3,4-丁烷四羧酸與2,2,6,6-四甲基-2,4,8,10-四氧雜螺[5.5]-十一烷-3,9-二乙醇2,2,6,6-四甲基-4-哌啶基酯之聚合物;雙(1-十一烷氧基-2,2,6,6-四甲基哌啶-4-基)碳酸酯;1-(2-羥基-2-甲基丙氧基)-2,2,6,6-四甲基-4-哌啶酚;1-(2-羥基-2-甲基丙氧基)-4-十八醯氧基-2,2,6,6-四甲基哌啶;1-(4-十八醯氧基-2,2,6,6-四甲基哌啶-1-基氧基)-2-十八醯氧基-2-甲基丙烷;1-(2-羥乙基)-2,2,6,6-四甲基-4-哌啶酚;1-(2-羥乙基)-2,2,6,6-四甲基-4-哌啶酚及二甲基琥珀酸酯之反應產物;2,2,4,4-四甲基-7-氧雜-3,20-二氮雜二螺[5.1.11.2]二十一烷-21-酮;2,2,6,6-四甲基-4-哌啶酚與高級脂肪酸之酯;3-十二烷基-1-(2,2,6,6-四甲基-4-哌啶基)吡咯啶-2,5-二酮;1-十八烷基-1H-吡咯-2,5-二酮與(1-甲基乙烯基)苯及1-(2,2,6,6-四甲基-4-哌
啶基)-1H-吡咯-2,5-二酮之聚合物;哌嗪酮,1,1',1"-[1,3,5-三嗪-2,4,6-三基參[(環己基亞胺基)-2,1-乙二基]]參[3,3,5,5-四甲基-;哌嗪酮,1,1',1"-[1,3,5-三嗪-2,4,6-三基參[(環己基亞胺基)-2,1-乙二基]]參[3,3,4,5,5-五甲基-;7,7,9,9-四甲基-2-環十一烷基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷及表氯醇之反應產物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-環己基胺基-2,6-二氯-1,3,5-三嗪之縮合物;1,2-雙(3-胺基丙胺基)乙烷、2,4,6-三氯-1,3,5-三嗪及4-丁基胺基-2,2,6,6-四甲基哌啶之縮合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-嗎啉基-2,6-二氯-1,3,5-三嗪之縮合物;2-氯-4,6-雙(4-正丁基胺基-2,2,6,6-四甲基哌啶基)-1,3,5-三嗪及1,2-雙(3-胺基丙胺基)乙烷之縮合物;2-氯-4,6-雙(4-正丁基胺基-1,2,2,6,6-五甲基哌啶基)-1,3,5-三嗪及1,2-雙-(3-胺基丙胺基)乙烷之縮合物;2-[(2-羥乙基)胺基]-4,6-雙[N-(1-環己氧基-2,2,6,6-四甲基哌啶-4-基)丁基胺基-1,3,5-三嗪;丙烷二酸[(4-甲氧基苯基)-亞甲基]-雙-(1,2,2,6,6-五甲基-4-哌啶基)酯;肆(2,2,6,6-四甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;3,5-雙(1,1-二甲基乙基)-4-羥基-苯丙酸1-[2-[3-[3,5-雙(1,1-二甲基乙基)-4-羥苯基]-1-側氧基丙氧基]乙基]-2,2,6,6-四甲基-4-哌啶基酯;N-(1-辛氧基-2,2,6,6-四甲基哌啶-4-基)-N'-十二烷基草醯胺;次氮基三乙酸參(2,2,6,6-四甲基哌啶-4-基)酯;1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(1,2,2,6,6-五甲基-4-哌啶基):1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(2,2,6,6-四甲基-4-哌啶基);1-(2-羥乙基)-2,2,6,6-四甲基-4-羥基哌啶及琥珀酸之縮合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-第三-辛基胺基-2,6-二氯-1,3,5-三嗪之縮合物;1,2,3,4-丁烷四羧酸1,2,2,6,6-五甲基-4-哌啶基十三烷基酯;肆(2,2,6,6-四甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;1,2,3,4-丁烷四羧酸2,2,6,6-四甲基-4-哌啶基十三烷基酯;肆(1,2,2,6,6-五甲基哌啶-4-基)-1,2,3,4-丁烷四羧
酸酯;2,2,4,4-四甲基-21-側氧基-7-氧雜-3.20-二氮雜螺(5.1.11.2)-二十一烷-20-丙酸-十二烷基酯及2,2,4,4-四甲基-21-側氧基-7-氧雜-3.20-二氮雜螺(5.1.11.2)-二十一烷-20-丙酸-十四烷基酯之混合物;1H,4H,5H,8H-2,3a,4a,6,7a,8a-六氮雜環戊烷并[def]茀-4,8-二酮,六氫-2,6-雙(2,2,6,6-四甲基-4-哌啶基)-;聚甲基[丙基-3-氧基(2',2',6',6'-四甲基-4,4'-哌啶基)]矽氧烷;聚甲基[丙基-3-氧基(1',2',2',6',6'-五甲基-4,4'-哌啶基)]矽氧烷;甲基丙烯酸甲酯與丙烯酸乙酯及2,2,6,6-四甲基哌啶-4-基丙烯酸酯之共聚物;混合C20至C24 α-烯烴及(2,2,6,6-四甲基哌啶-4-基)琥珀醯亞胺之共聚物;1,2,3,4-丁烷四羧酸與β,β,β',β'-四甲基-2,4,8,10-四氧雜螺[5.5]十一烷-3,9-二乙醇1,2,2,6,6-五甲基-4-哌啶基酯之聚合物;1,2,3,4-丁烷四羧酸與β,β,β',β'-四甲基-2,4,8,10-四氧雜螺[5.5]十一烷-3,9-二乙醇2,2,6,6-四甲基-4-哌啶基酯共聚物之聚合物;N,N'-雙(2,2,6,6-四甲基-4-哌啶基)-1,3-苯二羧醯胺;1,1'-(1,10-二側氧基-1,10-癸二基)-雙(六氫-2,2,4,4,6-五甲基嘧啶;N-(1-乙醯基-2,2,6,6-四甲基哌啶基)-N'-十二烷基乙二醯胺;N,N'-1,6-己二基雙[N-(2,2,6,6-四甲基-4-哌啶基)甲醯胺;1,3:2,4-雙-O-(2,2,6,6-四甲基-4-伸哌啶基)-D-葡萄糖醇;2,2,4,4-四甲基-7-氧雜-3,20-二氮雜-21-側氧基-二螺[5.1.11.2]二十一烷;2-甲基-N-(2,2,6,6-四甲基-4-哌啶基)-2-[(2,2,6,6-四甲基-4-哌啶基)胺基]-丙醯胺;2,2,4,4-四甲基-21-側氧基-7-氧雜-3,20-二氮雜二螺[5.1.11.2]二十一烷-20-丙酸十二烷基酯;N-(2,2,6,6-四甲基哌啶-4-基)-β-胺基丙酸十二烷基酯;N-(2,2,6,6-四甲基哌啶-4-基)-N'-胺基草醯胺;N-(2,2,6,6-四甲基-4-哌啶基)-3-[(2,2,6,6-四甲基-4-哌啶基)胺基]-丙醯胺;4-十六烷氧基-2,2,6,6-四甲基哌啶及4-硬脂基氧基-2,2,6,6-四甲基哌啶之混合物;3-十二烷基-1-(1,2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1-乙醯基-2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;琥珀酸雙(2,2,6,6-四甲基哌啶-4-
基)酯;3,5-二-第三丁基-4-羥基苄基丙二酸雙(1,2,2,6,6-五甲基哌啶-4-基)正丁基酯;次氮基三乙酸參(2,2,6,6-四甲基哌啶-4-基)酯;1,1'-(1,2-乙二基)雙(3,3,5,5-四甲基哌嗪酮);4-苯甲醯基-2,2,6,6-四甲基哌啶;4-硬脂基氧基-2,2,6,6-四甲基哌啶;雙(1,2,2,6,6-五甲基哌啶基)-2-正丁基-2-(2-羥基-3,5-二-第三丁基苄基)丙二酸酯;3-正辛基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸-2,4-二酮;癸二酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;琥珀酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;8-乙醯基-3-十二烷基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸烷-2,4-二酮;3-十二烷基-1-(2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1-乙醯基-2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1,2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;4-十六烷氧基-2,2,6,6-四甲基哌啶及4-硬脂基氧基-2,2,6,6-四甲基哌啶之混合物;2-十一烷基-7,7,9,9-四甲基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷;1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(2,2,6,6-四甲基-4-哌啶基)及1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(1,2,2,6,6-五甲基-4-哌啶基);N1-(β-羥乙基)3,3-五亞甲基-5,5-二甲基哌嗪-2-酮;N1-第三辛基-3,3,5,5-四甲基-二氮呯-2-酮;N1-第三辛基-3,3-五亞甲基-5,5-六亞甲基-二氮呯-2-酮;N1-第三辛基-3,3-五亞甲基-5,5-二甲基哌嗪-2-酮;反式-1,2-環己烷-雙-(N1-5,5-二甲基-3,3-五亞甲基-2-哌嗪酮;反式-1,2-環己烷-雙-(N1-3,3,5,5-二螺五亞甲基-2-哌嗪酮);N1-異丙基-1,4-二氮雜二螺-(3,3,5,5)五亞甲基-2-哌嗪酮;N1-異丙基-1,4-二氮雜二螺-3,3-五亞甲基-5,5-四亞甲基-2-哌嗪酮;N1-異丙基-5,5-二甲基-3,3-五亞甲基-2-哌嗪酮;反式-1,2-環己烷-雙-N1-(二甲基-3,3-五亞甲基-2-哌嗪酮);N1-辛基-5,5-二甲基-3,3-五亞甲基-1,4-二氮呯-2-酮;N1-辛基-1,4-二氮雜二螺-(3,3,5,5)五亞甲基-1,5-二氮呼-2-酮;及其混合物。
實施例7
如前述實施例中任一項之熱及UV光穩定組合物,其中該受阻羥基苯甲酸酯化合物係根據式(III):
其中式(III)中之R17係C1-C8烷基,且式(III)中之R18係C1-C24烷基或經取代或未經取代之C6-C24芳基。
實施例8
如前述實施例中任一項之熱及UV光穩定組合物,其中該受阻羥基苯甲酸酯化合物係選自由以下組成之群:3,5-二-第三丁基-4-羥基苯甲酸2,4-二-第三丁基苯基酯;3,5-二-第三丁基-4-羥基苯甲酸十六烷基酯;3,5-二-第三丁基-4-羥基苯甲酸十八烷基酯;3,5-二-第三丁基-4-羥基苯甲酸辛酯;3,5-二-第三丁基-4-羥基苯甲酸十四烷基酯;3,5-二-第三丁基-4-羥基苯甲酸山萮酯;3,5-二-第三丁基-4-羥基苯甲酸2-甲基-4,6-二-第三丁基苯基酯及3-[3-第三丁基-4-(3,5-二-第三丁基-4-羥基苯甲醯氧基)苯基]丙酸丁酯;及其混合物。
實施例9
如前述實施例中任一項之熱及UV光穩定組合物,其中該酸清除劑係選自由以下組成之群:氧化鋅、乳酸鈣、天然及合成水滑石、天然及合成水鋁鈣石、高級脂肪酸之鹼金屬鹽及鹼土金屬鹽、硬脂酸鈣、硬脂酸鋅、山萮酸鎂、硬脂酸鎂、硬脂酸鈉、蓖麻油酸鈉及棕櫚酸鉀、鄰苯二酚酸銻、鄰苯二酚酸鋅及其混合物。
實施例10
如前述實施例中任一項之熱及UV光穩定組合物,其中該受阻酚抗氧化劑化合物包含式(IVa)、(IVb)或(IVc)中一或多者之分子片段:
其中式(IVa)、(IVb)及(IVc)中之R18係選自氫及C1-4烴基;式(IVa)、(IVb)及(IVc)中之R19及R20各個別地選自氫及C1-C20烴基;且式(IVa)、(IVb)及(IVc)中之R37係選自C1-C12烴基。
實施例11
如實施例10之熱及UV光穩定組合物,其中式(IVa)、(IVb)及(IVc)中之R18及R37係選自甲基及第三丁基。
實施例12
如前述實施例中任一項之熱及UV光穩定組合物,其中該至少一種受阻酚化合物係選自:(1,3,5-參(4-第三丁基-3-羥基-2,6-二甲基苄基)-1,3,5-三嗪-2,4,6-(1H,3H,5H)-三酮;1,3,5-參(3,5-二-第三丁基-4-羥基苄基)-1,3,5-三嗪-2,4,6(1H,3H,5H)-三酮;1,1,3-參(2’-甲基-4’-羥基-5’-第三丁基苯基)丁烷;三乙二醇雙[3-(3-第三丁基-4-羥基-5-甲基苯基)丙酸酯];4,4’-硫基雙(2-第三丁基-5-甲基酚);2,2’-硫基二伸乙基雙[3-(3-第三丁基-4-羥基-5-甲基苯基)丙酸酯];3-(3’-第三丁基-4’-羥基-5’-甲基苯基)丙酸十八烷基酯;肆亞甲基(3-第三丁基-4-羥基-5-甲
基氫化肉桂酸酯)甲烷;N,N’-六亞甲基雙[3-(3-第三丁基-4-羥基-5-甲基苯基)丙醯胺];硫代二丙酸二(4-第三丁基-3-羥基-2,6-二甲基苄基酯);及3,5-二-(第三)丁基-4-羥基氫化肉桂酸十八烷基酯;及其混合物。
實施例13
如前述實施例中任一項之熱及UV光穩定組合物,其中該亞磷酸酯化合物係式(V)之受阻亞磷酸芳烷基酯化合物:
其中式(V)中之R1、R2、R3、R4、R5、R6、R7、R8、R9及R10各個別地選自氫、C1-C12烷基、C3-C12環烷基、C4-C12烷基環烷基、C6-C10芳基及C7-C12烷芳基,其中R1及R5總共包含至少5個碳,且R1及R5中之至少一者包含三級碳,其中R6及R10總共包含至少5個碳,且R6及R10中之至少一者包含三級碳;或
式(VI)之亞磷酸三芳基酯:
其中式(VI)中之R16、R17、R40、R41及R42各個別地選自氫、C1-C20烷基、C3-C20環烷基、C4-C20烷基環烷基、C6-C10芳基及C7-C20烷芳基;
或其混合物。
實施例14
如實施例13之熱及UV光穩定組合物,其中該受阻亞磷酸芳烷基酯係選自由以下組成之群:雙-(2,6-二-第三丁基-4-甲基苯基)季戊四醇二亞磷酸酯、(雙-(2,4-二異丙苯基)季戊四醇二亞磷酸酯、雙-(2,4-二-第三丁基-苯基)季戊四醇二亞磷酸酯及雙-(2,4,6-三-第三丁基-苯基)季戊四醇二亞磷酸酯;及其混合物。
實施例15
如實施例13之熱及UV光穩定組合物,其中該亞磷酸三芳基酯係選自由以下組成之群:亞磷酸參-(2,4-二-第三丁基苯基)酯、亞磷酸參(4-壬基苯基)酯及亞磷酸三苯基酯;及其混合物。
實施例16
如實施例2至15中任一項之熱及UV光穩定組合物,其中該硫酯化合物係選自由以下組成之群:硫代二丙酸二月桂基酯、硫代二丙酸二硬脂基酯、季戊四醇肆-(3-十二烷基硫代丙酸酯)、硫乙基硫代二琥珀酸四烷基酯、2,12-二羥基-4,10-二硫雜-7-氧雜十三亞甲基雙[3-(十二烷硫基)丙酸酯]、烷硫基-鏈烷酸之聚烷醇酯及3,3'-硫代二丙酸二烷基酯;及其混合物。
實施例17
如實施例2至16中任一項之熱及UV光穩定組合物,其中:該鄰-羥基參-芳基-s-三嗪化合物係2-[4,6-雙(2,4-二甲基苯基)-1,3,5-三嗪-2-基]-5-(辛氧基)苯酚;該受阻胺光穩定劑化合物係脂肪酸及C12-C21、C18不飽和2,2,6,6,-四甲基-4-哌啶基酯之混合物;該受阻羥基苯甲酸酯化合物係3,5-二-第三丁基-4-羥基苯甲酸十六烷基酯;
該酸清除劑係選自由以下組成之群:氧化鎂、氧化鋁、氫氧化鎂、氫氧化鋁、其碳酸鹽及其混合物;該亞磷酸酯化合物係雙(2,4-二異丙苯基)季戊四醇二亞磷酸酯);該受阻酚抗氧化劑化合物係1,3,5-參(4-第三丁基-3-羥基-2,6-二甲基苄基)-1,3,5-三嗪-2,4,6-(1H,3H,5H)-三酮;且該硫酯係季戊四醇肆-(3-十二烷基硫代丙酸酯)或硫代二丙酸二硬脂基酯。
實施例18
一種組合物,其包含:如實施例1至17中任一項之熱及UV光穩定組合物;及待穩定之物質。
實施例19
如實施例18之組合物,其中該待穩定之物質係選自由以下組成之群:聚烯烴、聚酯、聚醚、聚酮、聚醯胺、天然及合成橡膠、聚胺基甲酸酯、聚苯乙烯、耐衝擊聚苯乙烯、聚丙烯酸酯、聚甲基丙烯酸酯、聚縮醛、聚丙烯腈、聚丁二烯、聚苯乙烯、丙烯腈-丁二烯-苯乙烯、苯乙烯丙烯腈、丙烯酸酯苯乙烯丙烯腈、乙酸丁酸纖維素、纖維素聚合物、聚醯亞胺、聚醯胺醯亞胺、聚醚醯亞胺、聚苯硫醚、聚苯醚聚碸、聚醚碸、聚氯乙烯、聚碳酸酯、聚酮、脂族聚酮、熱塑性烯烴、胺基樹脂交聯聚丙烯酸酯及聚酯、聚異氰酸酯交聯聚酯及聚丙烯酸酯、苯酚/甲醛、脲/甲醛及三聚氰胺/甲醛樹脂、乾燥及非乾燥醇酸樹脂、醇酸樹脂、聚酯樹脂、與三聚氰胺樹脂、尿素樹脂、異氰酸酯、異氰尿酸酯、胺基甲酸酯及環氧樹脂交聯之丙烯酸酯樹脂、衍生自脂族、環脂族、雜環及芳族縮水甘油基化合物(其與酐或胺交聯)之交聯環氧樹脂、聚矽氧烷、邁克爾加成聚合物、胺、具有活性不飽和及亞甲基化合物之封端胺、具有活性不飽和及亞甲基化合物之酮亞胺、與不飽和丙烯酸聚乙醯乙酸酯樹脂組合之聚酮亞胺、與不飽和丙
烯酸樹脂組合之聚酮亞胺、輻射可固化組合物、環氧三聚氰胺樹脂、有機染料、化妝品、纖維素基紙調配物、照相軟片紙、纖維、蠟、油墨及其摻合物。
實施例20
如實施例18或實施例19之組合物,其中該待穩定之物質係選自由以下組成之群:熱塑性烯烴、丙烯腈-丁二烯-苯乙烯、聚酯、聚氯乙烯、聚醯胺、聚胺基甲酸酯或丙烯、異丁烯、丁烯、甲基戊烯、己烯、庚烯、辛烯、異戊二烯、丁二烯、己二烯、二環戊烷二烯、亞乙基環戊烯及降冰片烯之均聚物及共聚物。
實施例21
如實施例18至20中任一項之組合物,其中該待穩定之物質係聚丙烯或聚乙烯。
實施例22
如實施例18之組合物,其中該待穩定之物質係乙烯基擋板、乙烯基擋板邊飾、百葉窗、山墻通風口、屋簷、招牌、拱腹、模具、屋頂瓦、屋頂襯底、屋頂膜、板條系統、板條延伸件、防水板、瓦盤、屋脊通風口、露天磚、屋脊系統、屋簷立管、錐形帶、山墻端楔形物、傾斜邊飾、防滲膜、複合甲板材料、欄杆或窗框。
實施例23
如實施例18至21中任一項之組合物,其中該組合物係母料,且該熱及UV光穩定組合物基於該母料組合物之總重量計係以約10重量%至約80重量%之量存在,且該待穩定之物質基於該母料組合物之總重量計係以約20重量%至約90重量%之量存在。
實施例24
如實施例23之組合物,其中該組合物係母料,且該熱及UV光穩定組合物基於該母料組合物之總重量計係以約30重量%至約60重量%
之量存在,且該待穩定之物質基於該母料組合物之總重量計係以約40重量%至約70重量%之量存在。
實施例25
如實施例23至24中任一項之組合物,其中該組合物係母料,且該熱及UV光穩定組合物基於該母料組合物之總重量計係以介於約40重量%至約50重量%間之量存在,且該待穩定之物質基於該母料組合物之總重量計係以介於約50重量%至約60重量%間之量存在。
實施例26
如實施例18至22中任一項之組合物,其中基於該穩定組合物之總重量計,該熱及UV光穩定組合物係以0.01重量%至5重量%之量存在。
實施例27
如實施例26之組合物,其中基於該穩定組合物之總重量計,該熱及UV光穩定組合物係以0.05重量%至2重量%之量存在。
實施例28
如實施例26至27中任一項之組合物,其中基於該穩定組合物之總重量計,該鄰-羥基參-芳基-s-三嗪化合物之量係約0.002重量%至約0.50重量%,該受阻胺光穩定劑化合物之量係約0.01重量%至約1.20重量%,該受阻羥基苯甲酸酯化合物之量係約0.01重量%至約1.20重量%,該酸清除劑之量係約0.001重量%至約0.50重量%,該受阻酚抗氧化劑化合物之量係約0.001重量%至約0.50重量%,且該亞磷酸酯化合物之量係約0.005重量%至約1.00重量%。
實施例29
如實施例28之組合物,其中基於該穩定組合物之總重量計,該鄰-羥基參-芳基-s-三嗪化合物之量係約0.004重量%至約0.20重量%,該受阻胺光穩定劑化合物之量係約0.02重量%至約0.80重量%,該受
阻羥基苯甲酸酯化合物之量係約0.02重量%至約0.80重量%,該酸清除劑之量係約0.003重量%至約0.25重量%,該受阻酚抗氧化劑化合物之量係約0.002重量%至約0.25重量%,且該亞磷酸酯組合物之量係約0.01重量%至約0.80重量%。
實施例30
如實施例26至29中任一項之組合物,其中該熱及UV光穩定組合物另外包含硫酯化合物,其中基於該穩定組合物之總重量計,該硫酯化合物之量係約0.001重量%至約0.80重量%。
實施例31
如實施例30之組合物,其中基於該穩定組合物之總重量計,該硫酯化合物之量係約0.003重量%至約0.4重量%。
實施例32
一種製備如實施例18至31中任一項之組合物之方法,其中將該待穩定之物質與該熱及UV光穩定組合物組合。
實施例33
如實施例32之方法,其中該待穩定之物質係選自由以下組成之群:熱塑性烯烴、丙烯腈-丁二烯-苯乙烯、聚酯、聚氯乙烯、聚醯胺、聚胺基甲酸酯或丙烯、異丁烯、丁烯、甲基戊烯、己烯、庚烯、辛烯、異戊二烯、丁二烯、己二烯、二環戊烷二烯、亞乙基環戊烯及降冰片烯之均聚物及共聚物。
實施例34
如實施例32或實施例33之方法,其中該待穩定之物質係聚丙烯或聚乙烯。
實施例35
如實施例32之方法,其中該待穩定之物質係乙烯基擋板、乙烯基擋板邊飾、百葉窗、山墻通風口、屋簷、招牌、拱腹、模具、屋頂
瓦、屋頂襯底、屋頂膜、板條系統、板條延伸件、防水板、瓦盤、屋脊通風口、露天磚、屋脊系統、屋簷立管、錐形帶、山墻端楔形物、傾斜邊飾、防滲膜、複合甲板材料、欄杆或窗框。
實施例36
一種用於改良選自由下列組成之群之物質之可加工性之方法:聚烯烴、聚酯、聚醚、聚酮、聚醯胺、天然及合成橡膠、聚胺基甲酸酯、聚苯乙烯、耐衝擊聚苯乙烯、聚丙烯酸酯、聚甲基丙烯酸酯、聚縮醛、聚丙烯腈、聚丁二烯、聚苯乙烯、丙烯腈-丁二烯-苯乙烯、苯乙烯丙烯腈、丙烯酸酯苯乙烯丙烯腈、乙酸丁酸纖維素、纖維素聚合物、聚醯亞胺、聚醯胺醯亞胺、聚醚醯亞胺、聚苯硫醚、聚苯醚聚碸、聚醚碸、聚氯乙烯、聚碳酸酯、聚酮、脂族聚酮、熱塑性烯烴、胺基樹脂交聯聚丙烯酸酯及聚酯、聚異氰酸酯交聯聚酯及聚丙烯酸酯、苯酚/甲醛、脲/甲醛及三聚氰胺/甲醛樹脂、乾燥及非乾燥醇酸樹脂、醇酸樹脂、聚酯樹脂、與三聚氰胺樹脂、尿素樹脂、異氰酸酯、異氰尿酸酯、胺基甲酸酯及環氧樹脂交聯之丙烯酸酯樹脂、衍生自脂族、環脂族、雜環及芳族縮水甘油基化合物(其與酐或胺交聯)之交聯環氧樹脂、聚矽氧烷、邁克爾加成聚合物、胺、具有活性不飽和及亞甲基化合物之封端胺、具有活性不飽和及亞甲基化合物之酮亞胺、與不飽和丙烯酸聚乙醯乙酸酯樹脂組合之聚酮亞胺、與不飽和丙烯酸樹脂組合之聚酮亞胺、輻射可固化組合物、環氧三聚氰胺樹脂、有機染料、化妝品、纖維素基紙調配物、照相軟片紙、纖維、蠟、油墨及其摻合物,該方法包括向該物質添加穩定量之穩定組合物,該穩定組合物係如實施例1至17中任一項。
本文所揭示之組合物可用於各種應用中,包括(但不限於)汽車應用,諸如排氣孔、儀錶面板、控制臺、電池室、及外部部件(諸如保險桿、側飾條(side molding)及鏡罩)。該等組合物亦可用於防滲膜應
用中,諸如,例如,池塘內襯、地面覆蓋物、襯底(underlayment)、防水層、侵蝕控制膜等。本文亦涵蓋將受益於熱及UV穩定性之其他應用。
雖然已參考各種示例性實施例進行描述,但熟習此項技術者將理解,在不脫離本發明範圍下可作出各種改變,且可用等效物取代其元素。此外,可在不脫離本發明之基本範圍下作許多修改,以使特定情形或事件適應本發明教示。因此,希望本發明不限於以預期用於實施本發明之最佳模式所揭示之特定實施例,而是本發明將包括落於隨附申請專利範圍之範圍內之所有實施例。
實例1-14:
現將藉由以下實例說明本發明。該等實例無意限制本發明之範圍。結合上文一般及詳盡描述,該等實例進一步解讀本發明。
物質:使用Asahi Kasei Corporation之熱塑性烯烴(TPO)編號AHXPT053A1100NT101作為基質聚合物。下表1中列出此後將使用之各種添加劑(命名為A-H)及其重量%裝載量。該等添加劑係以收貨狀態使用。
聚合物添加劑之熔融混合:首先,稱重該等添加劑,並與聚合物顆粒混合。劇烈振盪固體混合物,以使添加劑均勻混合。然後,將固體混合物饋至雙螺桿擠出機料斗中。使用雙螺桿擠出機混合添加劑。混合期間的條件如下:轉子轉速:130rpm;熔融溫度:232℃;進料速度:800rpm;溫度分佈範圍:171-230℃。混合期間的平均壓力讀數為:36-40%。使用Conair製粒機將混合樣品製成顆粒。在進一步使用之前使該等顆粒風乾24小時。
製備樣品:使用Arburg注射成形機製備熱及耐候性測試樣品。注射成形期間的條件如下:噴嘴溫度:230℃;注射壓力:60;注入量:14.5。就拉伸測試而言,根據ASTM638-Type 5製備拉伸棒。使用具有標準尺寸2 x 2 x 0.125英寸之飾板(Plaque)進行熱及耐候性測試。
熱及耐候性測試條件:就熱性能而言,將樣品(測試棒及飾板)保持在150℃下,總共持續1000小時。分析樣品在200小時間隔下之光澤保留性、△E及機械強度(斷裂應力)。使用BYK-Gardner之micro-TRI-Gloss,按照ASTM測試程序D523以60°角測量表面光澤度。光澤保留性值係基於未曝露的樣品計算。使用Macbeth Color Eye色度計,利用ASTM D2244-79,以1”視野及D65/10°觀測器測量樣品顏色變化。由原始數據計算△E,其係曝露前後之總顏色變化之差異。△E越低表示顏色變化越小,說明性能更佳。就拉伸強度而言,在Instron Engineering Company拉伸測試儀(型號TTB)上測試各數據點之五根測試棒。使用ASTM D638類型-5法測量五個測試樣品之平均拉伸強度。拉伸測試儀之十字頭速度為2英寸(0.508cm)/分鐘。
就UV耐候性而言,在ASTM-G-155測試條件PV1303、SAEJ1885(J2412)及SAEJ1960(J2527)下將樣品曝露至Xenon耐候計。在設定曝露間隔後,分析樣品之光澤保留性及△E。
如上所述調配具有各種穩定劑添加劑組合之十三種樣品,且然後測試相對於對照樣品(未添加穩定劑組合物)之極端熱性能(拉伸強度、光澤度及顏色變化)及極端耐候性能(光澤度及顏色變化)。彼等以「C」表示之樣品係比較用,且代表對照樣品(亦即,未添加穩定組合物)或含先前為熟習此項技術者所知之調配物之樣品。例如,實例2C係基於美國專利案第6,843,939號中所述之調配物。下表2至5中呈現如上製備之樣品之熱及耐候性測試結果。
與本文所述之某些本發明組合物(例如,實例5-14)相比,實例1C-4C在極端熱條件下之保留拉伸強度性能表現較差。
就最高光澤保留性及最低顏色變化而言,與對照樣品及含熟習此項技術者所知之調配物之樣品(亦即,實例1C-4C)相比,如本文所述之本發明穩定組合物(例如,實例13及14)提供最佳極端熱性能。以肉眼觀察圖1A-1E亦證實此結果。無穩定劑組合物之飾板(圖1A)或具有基於US 6,843,939之穩定劑組合物之飾板(圖1B)在極端熱條件下顯
示溢流(blooming),而具有如本文所述之本發明穩定組合物之飾板(圖1C、1D及1E)在相同條件下顯示明顯更少或無溢流。
與對照樣品及含熟習此項技術者所知之調配物之樣品(亦即,實
例1C-4C)相比時,就最高光澤保留性而言,如本文所述之本發明穩定組合物(例如,實例10、13及14)不會不利地影響良好的耐候性能。
與對照樣品及含熟習此項技術者所知之調配物之樣品(亦即,實例1C-4C)相比時,就最低顏色變化而言,如本文所述之本發明穩定組
合物(例如,實例10、13及14)不會不利地影響良好的耐候性能。
因此,基於以上結果,出乎意料地顯示,如本文所述之本發明穩定組合物不僅顯示協同效果,且在極端條件下,與對照樣品及含熟習此項技術者所知之調配物之樣品相比,就保留拉伸強度而言提供增強的熱性能,而且如本文所述之本發明穩定組合物不具有含熟習此項技術者所知之調配物之樣品所呈現之針對良好耐候性能之任何拮抗效果。
實例15-19:多遍(Multipass)加工穩定性研究
在實例15-19中,使用表1中所列添加劑進行多遍加工穩定性研究。
聚合物添加劑之熔融混合:首先,稱重該等添加劑並與聚丙烯(Profax 6301)樹脂混合。劇烈振盪固體混合物,以達成添加劑之均勻混合。然後,將固體混合物饋至單螺桿擠出機料斗中。使用單螺桿擠出機混合添加劑。混合期間的條件如下:轉子轉速:100rpm;熔融溫度:230℃;進料速度:70-100rpm;溫度分佈範圍:215-230℃。混合期間的平均壓力讀數為:36-40%。使用Conair製粒機將混合樣品製成顆粒。
多遍擠壓加工:使顆粒通過單螺桿擠出機五次,並自第一遍、第遍及第五遍收集約200g樣品。為確定加工特性,使用Dynisco熔體指數測試儀(MFI)測量混合聚丙烯顆粒之相對熔體流動。此程序係針對ASTM D1238方法B-自動定時流速測量。較低熔體流速(MFR-g/10min)指示較高黏度性質,此證實聚合物之較佳穩定性性能。結果顯示於下表6及圖2中所示圖表中。
如表6及圖2圖表中所示,如本文所述之本發明穩定組合物(實例17、18及19)相較於其他組合物具有改良之可加工性,亦即,保持穩定並維持低熔體流動速率。
Claims (23)
- 一種熱及紫外(UV)光穩定組合物,其包含:鄰-羥基參-芳基-s-三嗪化合物;受阻胺光穩定劑化合物;受阻羥基苯甲酸酯化合物;酸清除劑;亞磷酸酯化合物;及受阻酚抗氧化劑化合物。
- 如請求項1之熱及UV光穩定組合物,其另外包含硫酯化合物。
- 如請求項2之熱及UV光穩定組合物,其中該硫酯化合物係選自由以下組成之群:硫代二丙酸二月桂基酯、硫代二丙酸二硬脂基酯、季戊四醇肆-(3-十二烷基硫代丙酸酯)、硫乙基硫代二琥珀酸四烷基酯、2,12-二羥基-4,10-二硫雜-7-氧雜十三亞甲基雙[3-(十二烷硫基)丙酸酯]、烷硫基-鏈烷酸之聚烷醇酯及3,3'-硫代二丙酸二烷基酯;及其混合物。
- 如請求項1之熱及UV光穩定組合物,其中:(a)該鄰-羥基參-芳基-s-三嗪化合物係式(I)之2-(2’-羥苯基)-1,3,5-三嗪化合物:
其中式(I)中之R34及R35各獨立地選自視情況經取代之C6-C10芳基、經C1-C10烴基取代之胺基、C1-C10醯基及C1-C10烷氧基;且 其中式(I)中在式I之苯氧基部分之位置0至4上之R36係相同或不同之取代基,且係獨立地選自羥基、C1-C12烴基、C1-C12烷氧基、C1-C12烷氧基酯及C1-C12醯基,(b)該受阻胺光穩定劑化合物包含式(II)之分子片段: 其中式(II)中之R31係選自:氫;OH;C1-C20烴基;-CH2CN;C1-C12醯基;及C1-C18烷氧基;式(II)中之R38係選自:氫;及C1-C8烴基;且式(II)中之R29、R30、R32及R33各獨立地選自C1-C20烴基,或式(II)中之R29及R30及/或R32及R33一起與附接至其之碳形成C5-C10環烷基;或式(IIa)之分子片段 其中式(IIa)中之m係1至2之整數;R39係選自:氫;OH;C1-C20烴基;-CH2CN;C1-C12醯基;及C1-C18烷氧基;且式(IIa)中之G1-G4各獨立地選自C1-C20烴基,(c)該受阻羥基苯甲酸酯化合物係根據式(III): 其中式(III)中之R17係C1-C8烷基,且式(III)中之R18係C1-C24烷基或經取代或未經取代之C6-C24芳基,(d)該酸清除劑係選自由以下組成之群:氧化鋅、乳酸鈣、天然及合成水滑石、天然及合成水鋁鈣石、高級脂肪酸之鹼金屬鹽及鹼土金屬鹽、硬脂酸鈣、硬脂酸鋅、山萮酸鎂、硬脂酸鎂、硬脂酸鈉、蓖麻油酸鈉及棕櫚酸鉀、鄰苯二酚酸銻、鄰苯二酚酸鋅及其混合物,(e)該受阻酚抗氧化劑化合物包含式(IVa)、(IVb)或(IVc)中一或多者之分子片段: 其中式(IVa)、(IVb)及(IVc)中之R18係選自氫及C1-4烴基;式(IVa)、(IVb)及(IVc)中之R19及R20各個別地選自氫及C1-C20烴基;且式(IVa)、(IVb)及(IVc)中之R37係選自C1-C12烴基,且(f)該亞磷酸酯化合物係式(V)之受阻亞磷酸芳烷基酯化合物: 其中式(V)中之R1、R2、R3、R4、R5、R6、R7、R8、R9及R10各個別地選自氫、C1-C12烷基、C3-C12環烷基、C4-C12烷基環烷基、C6-C10芳基及C7-C12烷芳基,其中R1及R5總共包含至少5個碳,且R1及R5中之至少一者包含三級碳,其中R6及R10總共包含至少5個碳,且R6及R10中之至少一者包含三級碳;或式(VI)之亞磷酸三芳基酯: 其中式(VI)中之R16、R17、R40、R41及R42各個別地選自氫、C1-C20烷基、C3-C20環烷基、C4-C20烷基環烷基、C6-C10芳基及C7-C20烷芳基;或其混合物。 - 如請求項4之熱及UV光穩定組合物,其中該2-(2’-羥苯基)-1,3,5-三嗪化合物係選自:4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4-辛氧基苯基)-s-三嗪;4,6-雙-(2,4-二甲基苯基)-2-(2,4-二羥苯基)-s-三嗪;2,4-雙(2,4-二羥苯基)-6-(4-氯苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-羥基-乙氧基)苯基]-6-(4-氯苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-羥基-4-(2-羥基-乙氧基)苯基]-6-(2,4-二甲基苯基)-s-三嗪;2,4-雙[2-羥基-4-(2-羥基乙氧基)苯基]-6-(4-溴苯基)-s-三嗪;2,4-雙[2- 羥基-4-(2-乙醯氧基乙氧基)苯基]-6-(4-氯苯基)-s-三嗪;2,4-雙(2,4-二羥苯基)-6-(2,4-二甲基苯基)-s-三嗪;2,4-雙(4-聯苯基)-6-[2-羥基-4-[(辛氧基羰基)亞乙基氧基]苯基]-s-三嗪;2,4-雙(4-聯苯基)-6-[2-羥基-4-(2-乙基己氧基)苯基]-s-三嗪;2-苯基-4-[2-羥基-4-(3-第二丁氧基-2-羥基丙氧基)苯基]-6-[2-羥基-4-(3-第二戊氧基-2-羥基丙氧基)苯基]-s-三嗪;2,4-雙(2,4-二甲基苯基)-6-[2-羥基-4(-3-苄氧基-2-羥基丙氧基)苯基]-s-三嗪;2,4-雙(2-羥基-4-正丁氧基苯基)-6-(2,4-二-正丁氧基苯基)-s-三嗪;2,4-雙(2,4-二甲基苯基)-6-[2-羥基-4-(3-壬氧基-2-羥基丙氧基)-5-α-異丙苯基]-s-三嗪;亞甲基雙-{2,4-雙(2,4-二甲基苯基)-6-[2-羥基-4-(3-丁氧基-2-羥基丙氧基)苯基]-s-三嗪};亞甲基橋聯之二聚體混合物,在位置3:5'、5:5'及3:3'以5:4:1之比例橋接;2,4,6-參(2-羥基-4-異辛氧基羰基亞異丙基氧基-苯基)-s-三嗪;2,4-雙(2,4-二甲基苯基)-6-(2-羥基-4-己氧基-5-α-異丙苯基)-s-三嗪;2-(2,4,6-三甲基苯基)-4,6-雙[2-羥基-4-(3-丁氧基-2-羥基丙氧基)苯基]-s-三嗪;2,4,6-參[2-羥基-4-(3-第二丁氧基-2-羥基丙氧基)-苯基]-s-三嗪;4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4-(3-十二烷氧基-2-羥基丙氧基)苯基)-s-三嗪及4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4-(3-十三烷氧基-2-羥基丙氧基)苯基)-s-三嗪之混合物;4,6-雙-(2,4-二甲基苯基)-2-(2-羥基-4(3-(2-乙基己氧基)-2-羥基丙氧基)-苯基)-s-三嗪;4,6-二苯基-2-(4-己氧基-2-羥苯基)-s-三嗪;2-(4,6-二苯基-1,3,5-三嗪-2-基)-5-[2-(2-乙基己醯氧基)乙氧基]苯酚;2,4,6-參(2-羥基-4-辛氧基苯基)-1,3,5-三嗪;丙酸2,2’,2”-[1,3,5-三嗪-2,4,6-三基參[(3-羥基-4,1-伸苯基)氧基]]參-1,1’,1”-三辛基酯;丙酸2-[4-[4,6-雙([1,1’-聯苯]-4-基)-1,3,5-三嗪-2基]-3-羥基苯氧基]-異辛基酯;及其組合。
- 如請求項4之熱及UV光穩定組合物,其中該受阻胺光穩定劑係選自:癸二酸雙(2,2,6,6-四甲基哌啶-4-基)酯;琥珀酸雙(2,2,6,6-四甲基哌啶-4-基)酯;癸二酸雙(1,2,2,6,6-五甲基哌啶-4-基)酯;癸二酸雙(1-辛氧基-2,2,6,6-四甲基哌啶-4-基)酯;3,5-二-第三丁基-4-羥基苄基丙二酸雙(1,2,2,6,6-五甲基哌啶-4-基)正丁基酯;1-(2-羥乙基)-2,2,6,6-四甲基-4-羥基哌啶及琥珀酸之縮合物;硬脂酸2,2,6,6-四甲基哌啶-4-基酯;十二烷酸2,2,6,6-四甲基哌啶-4-基酯;硬脂酸1,2,2,6,6-五甲基哌啶-4-基酯;十二烷酸1,2,2,6,6-五甲基哌啶-4-基酯;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-第三辛基胺基-2,6-二氯-1,3,5-三嗪之縮合物;次氮基三乙酸參(2,2,6,6-四甲基哌啶-4-基)酯;肆(2,2,6,6-四甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;4-苯甲醯基-2,2,6,6-四甲基哌啶;4-硬脂基氧基-2,2,6,6-四甲基哌啶;雙(1,2,2,6,6-五甲基哌啶基)-2-正丁基-2-(2-羥基-3,5-二-第三丁基苄基)丙二酸酯;3-正辛基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸-2,4-二酮;癸二酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;琥珀酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-嗎啉基-2,6-二氯-1,3,5-三嗪之縮合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及甲基化4-嗎啉基-2,6-二氯-1,3,5-三嗪之縮合物;2-氯-4,6-雙(4-正丁基胺基-2,2,6,6-四甲基哌啶基)-1,3,5-三嗪及1,2-雙(3-胺基丙胺基)乙烷之縮合物;2-氯-4,6-雙(4-正丁基胺基-1,2,2,6,6-五甲基哌啶基)-1,3,5-三嗪及1,2-雙-(3-胺基丙胺基)乙烷之縮合物;8-乙醯基-3-十二烷基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸烷-2,4-二酮;3-十二烷基-1-(2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1-乙醯基-2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1,2,2,6,6-五甲基哌啶- 4-基)吡咯啶-2,5-二酮;4-十六烷氧基-2,2,6,6-四甲基哌啶及4-硬脂基氧基-2,2,6,6-四甲基哌啶之混合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-環己基胺基-2,6-二氯-1,3,5-三嗪之縮合物;1,2-雙(3-胺基丙胺基)乙烷、2,4,6-三氯-1,3,5-三嗪及4-丁基胺基-2,2,6,6-四甲基哌啶之縮合物;2-十一烷基-7,7,9,9-四甲基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷;側氧基-哌嗪基-三嗪;7,7,9,9-四甲基-2-環十一烷基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷及表氯醇之反應產物;肆(2,2,6,6-四甲基-4-哌啶基)丁烷-1,2,3,4-四羧酸酯;1,2,3,4-丁烷四羧酸肆(1,2,2,6,6-五甲基-4-哌啶基)酯;1,2,3,4-丁烷四羧酸1,2,2,6,6-五甲基-4-哌啶基十三烷基酯;1,2,3,4-丁烷四羧酸2,2,6,6-四甲基-4-哌啶基十三烷基酯;1,2,3,4-丁烷四羧酸與2,2,6,6-四甲基-2,4,8,10-四氧雜螺[5.5]-十一烷-3,9-二乙醇1,2,2,6,6-五甲基-4-哌啶基酯之聚合物;1,2,3,4-丁烷四羧酸與2,2,6,6-四甲基-2,4,8,10-四氧雜螺[5.5]-十一烷-3,9-二乙醇2,2,6,6-四甲基-4-哌啶基酯之聚合物;雙(1-十一烷氧基-2,2,6,6-四甲基哌啶-4-基)碳酸酯;1-(2-羥基-2-甲基丙氧基)-2,2,6,6-四甲基-4-哌啶酚;1-(2-羥基-2-甲基丙氧基)-4-十八醯氧基-2,2,6,6-四甲基哌啶;1-(4-十八醯氧基-2,2,6,6-四甲基哌啶-1-基氧基)-2-十八醯氧基-2-甲基丙烷;1-(2-羥乙基)-2,2,6,6-四甲基-4-哌啶酚;1-(2-羥乙基)-2,2,6,6-四甲基-4-哌啶酚及二甲基琥珀酸酯之反應產物;2,2,4,4-四甲基-7-氧雜-3,20-二氮雜二螺[5.1.11.2]二十一烷-21-酮;2,2,6,6-四甲基-4-哌啶酚與高級脂肪酸之酯;3-十二烷基-1-(2,2,6,6-四甲基-4-哌啶基)吡咯啶-2,5-二酮;1-十八烷基-1H-吡咯-2,5-二酮與(1-甲基乙烯基)苯及1-(2,2,6,6-四甲基-4-哌啶基)-1H-吡咯-2,5-二酮之聚合物;哌嗪酮,1,1',1"-[1,3,5-三嗪-2,4,6-三基參[(環己基亞胺基)-2,1-乙二 基]]參[3,3,5,5-四甲基-;哌嗪酮,1,1',1"-[1,3,5-三嗪-2,4,6-三基參[(環己基亞胺基)-2,1-乙二基]]參[3,3,4,5,5-五甲基-;7,7,9,9-四甲基-2-環十一烷基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷及表氯醇之反應產物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-環己基胺基-2,6-二氯-1,3,5-三嗪之縮合物;1,2-雙(3-胺基丙胺基)乙烷、2,4,6-三氯-1,3,5-三嗪及4-丁基胺基-2,2,6,6-四甲基哌啶之縮合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-嗎啉基-2,6-二氯-1,3,5-三嗪之縮合物;2-氯-4,6-雙(4-正丁基胺基-2,2,6,6-四甲基哌啶基)-1,3,5-三嗪及1,2-雙(3-胺基丙胺基)乙烷之縮合物;2-氯-4,6-雙(4-正丁基胺基-1,2,2,6,6-五甲基哌啶基)-1,3,5-三嗪及1,2-雙-(3-胺基丙胺基)乙烷之縮合物;2-[(2-羥乙基)胺基]-4,6-雙[N-(1-環己氧基-2,2,6,6-四甲基哌啶-4-基)丁基胺基-1,3,5-三嗪;丙烷二酸[(4-甲氧基苯基)-亞甲基]-雙-(1,2,2,6,6-五甲基-4-哌啶基)酯;肆(2,2,6,6-四甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;3,5-雙(1,1-二甲基乙基)-4-羥基-苯丙酸1-[2-[3-[3,5-雙(1,1-二甲基乙基)-4-羥苯基]-1-側氧基丙氧基]乙基]-2,2,6,6-四甲基-4-哌啶基酯;N-(1-辛氧基-2,2,6,6-四甲基哌啶-4-基)-N'-十二烷基草醯胺;次氮基三乙酸參(2,2,6,6-四甲基哌啶-4-基)酯;1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(1,2,2,6,6-五甲基-4-哌啶基):1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(2,2,6,6-四甲基-4-哌啶基);1-(2-羥乙基)-2,2,6,6-四甲基-4-羥基哌啶及琥珀酸之縮合物;N,N'-雙(2,2,6,6-四甲基哌啶-4-基)六亞甲基二胺及4-第三辛基胺基-2,6-二氯-1,3,5-三嗪之縮合物;1,2,3,4-丁烷四羧酸1,2,2,6,6-五甲基-4-哌啶基十三烷基酯;肆(2,2,6,6-四甲基哌啶-4-基)-1,2,3,4-丁烷四羧酸酯;1,2,3,4-丁烷四羧酸2,2,6,6-四甲基-4-哌啶基十三烷基酯;肆(1,2,2,6,6-五甲基哌啶-4-基)-1,2,3,4- 丁烷四羧酸酯;2,2,4,4-四甲基-21-側氧基-7-氧雜-3.20-二氮雜螺(5.1.11.2)-二十一烷-20-丙酸-十二烷基酯及2,2,4,4-四甲基-21-側氧基-7-氧雜-3.20-二氮雜螺(5.1.11.2)-二十一烷-20-丙酸-十四烷基酯之混合物;1H,4H,5H,8H-2,3a,4a,6,7a,8a-六氮雜環戊烷并[def]茀-4,8-二酮,六氫-2,6-雙(2,2,6,6-四甲基-4-哌啶基)-;聚甲基[丙基-3-氧基(2',2',6',6'-四甲基-4,4'-哌啶基)]矽氧烷;聚甲基[丙基-3-氧基(1',2',2',6',6'-五甲基-4,4'-哌啶基)]矽氧烷;甲基丙烯酸甲酯與丙烯酸乙酯及2,2,6,6-四甲基哌啶-4-基丙烯酸酯之共聚物;混合C20至C24 α-烯烴及(2,2,6,6-四甲基哌啶-4-基)琥珀醯亞胺之共聚物;1,2,3,4-丁烷四羧酸與β,β,β',β'-四甲基-2,4,8,10-四氧雜螺[5.5]十一烷-3,9-二乙醇1,2,2,6,6-五甲基-4-哌啶基酯之聚合物;1,2,3,4-丁烷四羧酸與β,β,β',β'-四甲基-2,4,8,10-四氧雜螺[5.5]十一烷-3,9-二乙醇2,2,6,6-四甲基-4-哌啶基酯共聚物之聚合物;N,N'-雙(2,2,6,6-四甲基-4-哌啶基)-1,3-苯二羧醯胺;1,1'-(1,10-二側氧基-1,10-癸二基)-雙(六氫-2,2,4,4,6-五甲基嘧啶;N-(1-乙醯基-2,2,6,6-四甲基哌啶基)-N'-十二烷基乙二醯胺;N,N'-1,6-己二基雙[N-(2,2,6,6-四甲基-4-哌啶基)甲醯胺;1,3:2,4-雙-O-(2,2,6,6-四甲基-4-伸哌啶基)-D-葡萄糖醇;2,2,4,4-四甲基-7-氧雜-3,20-二氮雜-21-側氧基-二螺[5.1.11.2]二十一烷;2-甲基-N-(2,2,6,6-四甲基-4-哌啶基)-2-[(2,2,6,6-四甲基-4-哌啶基)胺基]-丙醯胺;2,2,4,4-四甲基-21-側氧基-7-氧雜-3,20-二氮雜二螺[5.1.11.2]二十一烷-20-丙酸十二烷基酯;N-(2,2,6,6-四甲基哌啶-4-基)-β-胺基丙酸十二烷基酯;N-(2,2,6,6-四甲基哌啶-4-基)-N'-胺基草醯胺;N-(2,2,6,6-四甲基-4-哌啶基)-3-[(2,2,6,6-四甲基-4-哌啶基)胺基]-丙醯胺;4-十六烷氧基-2,2,6,6-四甲基哌啶及4-硬脂基氧基-2,2,6,6-四甲基哌啶之混合物;3-十二烷基-1-(1,2,2,6,6-五甲基哌 啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1-乙醯基-2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;琥珀酸雙(2,2,6,6-四甲基哌啶-4-基)酯;3,5-二-第三丁基-4-羥基苄基丙二酸雙(1,2,2,6,6-五甲基哌啶-4-基)正丁基酯;次氮基三乙酸參(2,2,6,6-四甲基哌啶-4-基)酯;1,1'-(1,2-乙二基)雙(3,3,5,5-四甲基哌嗪酮);4-苯甲醯基-2,2,6,6-四甲基哌啶;4-硬脂基氧基-2,2,6,6-四甲基哌啶;雙(1,2,2,6,6-五甲基哌啶基)-2-正丁基-2-(2-羥基-3,5-二-第三丁基苄基)丙二酸酯;3-正辛基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸-2,4-二酮;癸二酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;琥珀酸雙(1-辛氧基-2,2,6,6-四甲基哌啶基)酯;8-乙醯基-3-十二烷基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸烷-2,4-二酮;3-十二烷基-1-(2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1-乙醯基-2,2,6,6-四甲基哌啶-4-基)吡咯啶-2,5-二酮;3-十二烷基-1-(1,2,2,6,6-五甲基哌啶-4-基)吡咯啶-2,5-二酮;4-十六烷氧基-2,2,6,6-四甲基哌啶及4-硬脂基氧基-2,2,6,6-四甲基哌啶之混合物;2-十一烷基-7,7,9,9-四甲基-1-氧雜-3,8-二氮雜-4-側氧基螺[4.5]癸烷;1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(2,2,6,6-四甲基-4-哌啶基)及1,5-二氧雜螺{5,5}十一烷-3,3-二羧酸,雙(1,2,2,6,6-五甲基-4-哌啶基);N1(β-羥乙基)3,3-五亞甲基-5,5-二甲基哌嗪-2-酮;N1第三辛基-3,3,5,5-四甲基-二氮呼-2-酮;N1-第三辛基-3,3-五亞甲基-5,5-六亞甲基-二氮呯-2-酮;N1-第三-辛基-3,3-五亞甲基-5,5-二甲基哌嗪-2-酮;反式-1,2-環己烷-雙-(N1-5,5-二甲基-3,3-五亞甲基-2-哌嗪酮;反式-1,2-環己烷-雙-(N1-3,3,5,5-二螺五亞甲基-2-哌嗪酮);N1-異丙基-1,4-二氮雜二螺-(3,3,5,5)五亞甲基-2-哌嗪酮;N1-異丙基-1,4-二氮雜二螺-3,3-五亞甲基-5,5-四亞甲基-2-哌嗪酮;N1-異丙基-5,5-二甲基-3,3-五亞 甲基-2-哌嗪酮;反式-1,2-環己烷-雙-N1-(二甲基-3,3-五亞甲基-2-哌嗪酮);N1-辛基-5,5-二甲基-3,3-五亞甲基-1,4-二氮呼-2-酮;N1-辛基-1,4-二氮雜二螺-(3,3,5,5)五亞甲基-1,5-二氮呯-2-酮;及其混合物。
- 如請求項4之熱及UV光穩定組合物,其中該受阻羥基苯甲酸酯化合物係選自由以下組成之群:3,5-二-第三丁基-4-羥基苯甲酸2,4-二-第三丁基苯基酯;3,5-二-第三丁基-4-羥基苯甲酸十六烷基酯;3,5-二-第三丁基-4-羥基苯甲酸十八烷基酯;3,5-二-第三丁基-4-羥基苯甲酸辛酯;3,5-二-第三丁基-4-羥基苯甲酸十四烷基酯;3,5-二-第三丁基-4-羥基苯甲酸山萮酯;3,5-二-第三丁基-4-羥基苯甲酸2-甲基-4,6-二-第三丁基苯基酯及3-[3-第三丁基-4-(3,5-二-第三丁基-4-羥基苯甲醯氧基)苯基]丙酸丁酯;及其混合物。
- 如請求項4之熱及UV光穩定組合物,其中該至少一種受阻酚化合物係選自:(1,3,5-參(4-第三丁基-3-羥基-2,6-二甲基苄基)-1,3,5-三嗪-2,4,6-(1H,3H,5H)-三酮;1,3,5-參(3,5-二-第三丁基-4-羥基苄基)-1,3,5-三嗪-2,4,6(1H,3H,5H)-三酮;1,1,3-參(2’-甲基-4’-羥基-5’-第三丁基苯基)丁烷;三乙二醇雙[3-(3-第三丁基-4-羥基-5-甲基苯基)丙酸酯];4,4’-硫基雙(2-第三丁基-5-甲基酚);2,2’-硫基二伸乙基雙[3-(3-第三丁基-4-羥基-5-甲基苯基)丙酸酯];3-(3’-第三丁基-4’-羥基-5’-甲基苯基)丙酸十八烷基酯;肆亞甲基(3-第三丁基-4-羥基-5-甲基氫化肉桂酸酯)甲烷;N,N’-六亞甲基雙[3-(3-第三丁基-4-羥基-5-甲基苯基)丙醯胺];硫代二丙酸二(4-第三丁基-3-羥基-2,6-二甲基苄基酯);及3,5-二-(第三)丁基-4-羥基氫化肉桂酸十八烷基酯;及其混合物。
- 如請求項4之熱及UV光穩定組合物,其中該受阻亞磷酸芳烷基酯 係選自由以下組成之群:雙-(2,6-二-第三丁基-4-甲基苯基)季戊四醇二亞磷酸酯、(雙-(2,4-二異丙苯基)季戊四醇二亞磷酸酯、雙-(2,4-二-第三丁基-苯基)季戊四醇二亞磷酸酯及雙-(2,4,6-三-第三丁基-苯基)季戊四醇二亞磷酸酯;及其混合物。
- 如請求項4之熱及UV光穩定組合物,其中該亞磷酸三芳基酯係選自由以下組成之群:亞磷酸參-(2,4-二-第三丁基苯基)酯、亞磷酸參(4-壬基苯基)酯及亞磷酸三苯基酯;及其混合物。
- 如請求項2之熱及UV光穩定組合物,其中:該鄰-羥基參-芳基-s-三嗪化合物係2-[4,6-雙(2,4-二甲基苯基)-1,3,5-三嗪-2-基]-5-(辛氧基)苯酚;該受阻胺光穩定劑化合物係脂肪酸及C12-C21、C18不飽和2,2,6,6,-四甲基-4-哌啶基酯之混合物;該受阻羥基苯甲酸酯化合物係3,5-二-第三丁基-4-羥基苯甲酸十六烷基酯;該酸清除劑係選自由以下組成之群:氧化鎂、氧化鋁、氫氧化鎂、氫氧化鋁、其碳酸鹽及其混合物;該亞磷酸酯化合物係雙(2,4-二異丙苯基)季戊四醇二亞磷酸酯);該受阻酚抗氧化劑化合物係1,3,5-參(4-第三丁基-3-羥基-2,6-二甲基苄基)-1,3,5-三嗪-2,4,6-(1H,3H,5H)-三酮;且該硫酯係季戊四醇肆-(3-十二烷基硫代丙酸酯)或硫代二丙酸二硬脂基酯。
- 一種組合物,其包含:如請求項1之熱及UV光穩定組合物;及待穩定之物質。
- 如請求項12之組合物,其中該待穩定之物質係選自由以下組成 之群:聚烯烴、聚酯、聚醚、聚酮、聚醯胺、天然及合成橡膠、聚胺基甲酸酯、聚苯乙烯、耐衝擊聚苯乙烯、聚丙烯酸酯、聚甲基丙烯酸酯、聚縮醛、聚丙烯腈、聚丁二烯、聚苯乙烯、丙烯腈-丁二烯-苯乙烯、苯乙烯丙烯腈、丙烯酸酯苯乙烯丙烯腈、乙酸丁酸纖維素、纖維素聚合物、聚醯亞胺、聚醯胺醯亞胺、聚醚醯亞胺、聚苯硫醚、聚苯醚聚碸、聚醚碸、聚氯乙烯、聚碳酸酯、聚酮、脂族聚酮、熱塑性烯烴、胺基樹脂交聯聚丙烯酸酯及聚酯、聚異氰酸酯交聯聚酯及聚丙烯酸酯、苯酚/甲醛、脲/甲醛及三聚氰胺/甲醛樹脂、乾燥及非乾燥醇酸樹脂、醇酸樹脂、聚酯樹脂、與三聚氰胺樹脂、尿素樹脂、異氰酸酯、異氰尿酸酯、胺基甲酸酯及環氧樹脂交聯之丙烯酸酯樹脂、衍生自脂族、環脂族、雜環及芳族縮水甘油基化合物(其與酐或胺交聯)之交聯環氧樹脂、聚矽氧烷、邁克爾加成聚合物、胺、具有活性不飽和及亞甲基化合物之封端胺、具有活性不飽和及亞甲基化合物之酮亞胺、與不飽和丙烯酸聚乙醯乙酸酯樹脂組合之聚酮亞胺、與不飽和丙烯酸樹脂組合之聚酮亞胺、輻射可固化組合物、環氧三聚氰胺樹脂、有機染料、化妝品、纖維素基紙調配物、照相軟片紙、纖維、蠟、油墨及其摻合物。
- 如請求項12之組合物,其中該待穩定之物質係選自由以下組成之群:熱塑性烯烴、丙烯腈-丁二烯-苯乙烯、聚酯、聚氯乙烯、聚醯胺、聚胺基甲酸酯或丙烯、異丁烯、丁烯、甲基戊烯、己烯、庚烯、辛烯、異戊二烯、丁二烯、己二烯、二環戊烷二烯、亞乙基環戊烯及降冰片烯之均聚物及共聚物。
- 如請求項12之組合物,其中該待穩定之物質係乙烯基擋板、乙烯基擋板邊飾、百葉窗、山墻通風口、屋簷、招牌、拱腹、模具、屋頂瓦、屋頂襯底、屋頂膜、板條系統、板條延伸件、防 水板、瓦盤、屋脊通風口、露天磚、屋脊系統、屋簷立管、錐形帶、山墻端楔形物、傾斜邊飾、防滲膜、複合甲板材料、欄杆或窗框。
- 如請求項12之組合物,其中該組合物係母料,且該熱及UV光穩定組合物基於該母料組合物之總重量計係以約10重量%至約80重量%之量存在,且該待穩定之物質基於該母料組合物之總重量計係以約20重量%至約90重量%之量存在。
- 如請求項12之組合物,其中基於該穩定組合物之總重量計,該熱及UV光穩定組合物係以0.01重量%至5重量%之量存在。
- 如請求項17之組合物,其中基於該穩定組合物之總重量計,該鄰-羥基參-芳基-s-三嗪化合物之量係約0.002重量%至約0.50重量%,該受阻胺光穩定劑化合物之量係約0.01重量%至約1.20重量%,該受阻羥基苯甲酸酯化合物之量係約0.01重量%至約1.20重量%,該酸清除劑之量係約0.001重量%至約0.50重量%,該受阻酚抗氧化劑化合物之量係約0.001重量%至約0.50重量%,且該亞磷酸酯化合物之量係約0.005重量%至約1.00重量%。
- 如請求項12之組合物,其中該熱及UV光穩定組合物另外包含硫酯化合物,其中基於該穩定組合物之總重量計,該硫酯化合物之量係約0.001重量%至約0.80重量%。
- 一種製備如請求項12之組合物之方法,該方法包括:將該待穩定之物質與該熱及UV光穩定組合物組合在一起。
- 如請求項20之方法,其中該待穩定之物質係選自由以下組成之群:熱塑性烯烴、丙烯腈-丁二烯-苯乙烯、聚酯、聚氯乙烯、聚醯胺、聚胺基甲酸酯或丙烯、異丁烯、丁烯、甲基戊烯、己烯、庚烯、辛烯、異戊二烯、丁二烯、己二烯、二環戊烷二烯、亞乙基環戊烯及降冰片烯之均聚物及共聚物。
- 如請求項20之方法,其中該待穩定之物質係乙烯基擋板、乙烯基擋板邊飾、百葉窗、山墻通風口、屋簷、招牌、拱腹、模具、屋頂瓦、屋頂襯底、屋頂膜、板條系統、板條延伸件、防水板、瓦盤、屋脊通風口、露天磚、屋脊系統、屋簷立管、錐形帶、山墻端楔形物、傾斜邊飾、防滲膜、複合甲板材料、欄杆或窗框。
- 一種用於改良物質之可加工性之方法,該物質係選自由以下組成之群:聚烯烴、聚酯、聚醚、聚酮、聚醯胺、天然及合成橡膠、聚胺基甲酸酯、聚苯乙烯、耐衝擊聚苯乙烯、聚丙烯酸酯、聚甲基丙烯酸酯、聚縮醛、聚丙烯腈、聚丁二烯、聚苯乙烯、丙烯腈-丁二烯-苯乙烯、苯乙烯丙烯腈、丙烯酸酯苯乙烯丙烯腈、乙酸丁酸纖維素、纖維素聚合物、聚醯亞胺、聚醯胺醯亞胺、聚醚醯亞胺、聚苯硫醚、聚苯醚聚碸、聚醚碸、聚氯乙烯、聚碳酸酯、聚酮、脂族聚酮、熱塑性烯烴、胺基樹脂交聯聚丙烯酸酯及聚酯、聚異氰酸酯交聯聚酯及聚丙烯酸酯、苯酚/甲醛、脲/甲醛及三聚氰胺/甲醛樹脂、乾燥及非乾燥醇酸樹脂、醇酸樹脂、聚酯樹脂、與三聚氰胺樹脂、尿素樹脂、異氰酸酯、異氰尿酸酯、胺基甲酸酯及環氧樹脂交聯之丙烯酸酯樹脂、衍生自脂族、環脂族、雜環及芳族縮水甘油基化合物(其與酐或胺交聯)之交聯環氧樹脂、聚矽氧烷、邁克爾加成聚合物、胺、具有活性不飽和及亞甲基化合物之封端胺、具有活性不飽和及亞甲基化合物之酮亞胺、與不飽和丙烯酸聚乙醯乙酸酯樹脂組合之聚酮亞胺、與不飽和丙烯酸樹脂組合之聚酮亞胺、輻射可固化組合物、環氧三聚氰胺樹脂、有機染料、化妝品、纖維素基紙調配物、照相軟片紙、纖維、蠟、油墨及其摻合物,該方法包括向該物質添加穩定量之穩定組合物,該穩定組合物係如請求項1。
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| CN116120631B (zh) * | 2023-02-03 | 2025-06-13 | 天津利安隆新材料股份有限公司 | 抗老化剂组合物及其应用和抗老化高分子材料 |
| CN120936656A (zh) | 2023-04-05 | 2025-11-11 | 巴斯夫欧洲公司 | Uv光稳定剂 |
| WO2025099141A1 (en) | 2023-11-10 | 2025-05-15 | Cytec Industries Inc. | Stabilizing compositions for polymeric materials |
| WO2025099143A1 (en) | 2023-11-10 | 2025-05-15 | Cytec Industries Inc. | Compositions for stabilizing polymeric materials against uv light thermal and gas fading degradation |
| WO2025172192A1 (en) | 2024-02-15 | 2025-08-21 | Basf Se | Uv light stabilizers |
| WO2025219501A1 (en) * | 2024-04-17 | 2025-10-23 | Cytec Industries Inc. | Stabilizing compositions for polymeric materials |
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| US5214084A (en) * | 1990-03-14 | 1993-05-25 | Sumitomo Chemical Company, Ltd. | Stabilized polypropylene resin composition |
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| US6727300B2 (en) * | 2000-11-03 | 2004-04-27 | Cytec Technology Corp. | Polymeric articles containing hindered amine light stabilizers based on multi-functional carbonyl compounds |
| AU2002348236A1 (en) * | 2001-12-27 | 2003-07-24 | Cytec Technology Corp. | Uv stabilized thermoplastic olefins |
| KR20060015627A (ko) * | 2003-05-27 | 2006-02-17 | 시바 스페셜티 케미칼스 홀딩 인크. | 아미노아릴-1,3,5-트리아진 및 자외선 흡수제로서의 이의용도 |
| EP1680463A2 (en) * | 2003-11-03 | 2006-07-19 | Ciba SC Holding AG | Stabilizer compositions for halogen containing polymers |
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| EP2647664A1 (en) * | 2012-04-04 | 2013-10-09 | Cytec Technology Corp. | Method for stabilizing polyolefin films against UV degradation |
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- 2015-04-30 BR BR112016025445-7A patent/BR112016025445B1/pt active IP Right Grant
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI880896B (zh) * | 2018-08-22 | 2025-04-21 | 德商巴地斯顏料化工廠 | 經穩定之旋轉成型聚烯烴 |
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| CN106471049A (zh) | 2017-03-01 |
| CA2947699A1 (en) | 2015-11-05 |
| WO2015168389A1 (en) | 2015-11-05 |
| BR112016025445A2 (pt) | 2017-08-15 |
| EP3137540A1 (en) | 2017-03-08 |
| US20170349730A1 (en) | 2017-12-07 |
| JP6731910B2 (ja) | 2020-07-29 |
| US10407563B2 (en) | 2019-09-10 |
| CN106471049B (zh) | 2018-12-14 |
| US20150315465A1 (en) | 2015-11-05 |
| MX390673B (es) | 2025-03-21 |
| BR112016025445B1 (pt) | 2022-08-02 |
| KR101915874B1 (ko) | 2018-11-06 |
| JP2017518430A (ja) | 2017-07-06 |
| BR112016025445A8 (pt) | 2021-05-04 |
| EP3137540B1 (en) | 2024-10-30 |
| KR20160147279A (ko) | 2016-12-22 |
| ES3004696T3 (en) | 2025-03-12 |
| US9725579B2 (en) | 2017-08-08 |
| TWI685558B (zh) | 2020-02-21 |
| MX2016014351A (es) | 2017-05-30 |
| SA516380205B1 (ar) | 2020-12-31 |
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