TW202010826A - 經光安定化之聚烯烴膜、帶及單纖絲 - Google Patents
經光安定化之聚烯烴膜、帶及單纖絲 Download PDFInfo
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- TW202010826A TW202010826A TW108144113A TW108144113A TW202010826A TW 202010826 A TW202010826 A TW 202010826A TW 108144113 A TW108144113 A TW 108144113A TW 108144113 A TW108144113 A TW 108144113A TW 202010826 A TW202010826 A TW 202010826A
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- Prior art keywords
- butyl
- bis
- tert
- hydroxy
- group
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- FHAFFFSIDLDWQA-UHFFFAOYSA-N n-hexadecyloctadecan-1-imine oxide Chemical compound CCCCCCCCCCCCCCCCCC=[N+]([O-])CCCCCCCCCCCCCCCC FHAFFFSIDLDWQA-UHFFFAOYSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
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- 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
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- SLYJXPKHTZCZOG-UHFFFAOYSA-N n-tetradecyltetradecan-1-imine oxide Chemical compound CCCCCCCCCCCCCC[N+]([O-])=CCCCCCCCCCCCCC SLYJXPKHTZCZOG-UHFFFAOYSA-N 0.000 description 1
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- IJRHDFLHUATAOS-DPMBMXLASA-M sodium ricinoleate Chemical compound [Na+].CCCCCC[C@@H](O)C\C=C/CCCCCCCC([O-])=O IJRHDFLHUATAOS-DPMBMXLASA-M 0.000 description 1
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- 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
- 238000012360 testing method Methods 0.000 description 1
- LVEOKSIILWWVEO-UHFFFAOYSA-N tetradecyl 3-(3-oxo-3-tetradecoxypropyl)sulfanylpropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCC LVEOKSIILWWVEO-UHFFFAOYSA-N 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
- 239000004408 titanium dioxide Substances 0.000 description 1
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- SHEXSXZCZQBTFI-UHFFFAOYSA-N tridecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)-2-sulfanylpropanoate Chemical compound CCCCCCCCCCCCCOC(=O)C(S)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SHEXSXZCZQBTFI-UHFFFAOYSA-N 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
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 125000002948 undecyl 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])[H] 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
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- 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 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
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Classifications
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
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- C08K5/34—Heterocyclic compounds having nitrogen in the ring
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- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
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- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
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- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/88—Thermal treatment of the stream of extruded material, e.g. cooling
- B29C48/919—Thermal treatment of the stream of extruded material, e.g. cooling using a bath, e.g. extruding into an open bath to coagulate or cool the material
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- B—PERFORMING OPERATIONS; TRANSPORTING
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- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
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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
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- C08J5/18—Manufacture of films or sheets
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- 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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- C08K5/34922—Melamine; Derivatives thereof
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
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- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2023/00—Use of polyalkenes or derivatives thereof as moulding material
- B29K2023/10—Polymers of propylene
- B29K2023/12—PP, i.e. polypropylene
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- C—CHEMISTRY; METALLURGY
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/04—Homopolymers or copolymers of ethene
- C08J2323/06—Polyethene
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- 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
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
- C08J2323/10—Homopolymers or copolymers of propene
- C08J2323/12—Polypropene
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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
- C08K2201/00—Specific properties of additives
- C08K2201/014—Additives containing two or more different additives of the same subgroup in C08K
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/12—Applications used for fibers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacturing & Machinery (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Textile Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Artificial Filaments (AREA)
- Woven Fabrics (AREA)
- Plural Heterocyclic Compounds (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Cosmetics (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
本發明係關於降低在生產期間穿過水浴之經光安定化之聚烯烴膜、帶或單纖絲之水騰帶之方法、根據該方法製造之聚烯烴膜、帶或單纖絲及特定光安定劑用於降低經光安定化之聚烯烴膜、帶或單纖絲之水騰帶之用途。
用於生產聚烯烴膜、帶或單纖絲之普遍方法在於將聚合物熔體擠出穿過適宜裝置並以膜、帶或單纖絲之形式進入至水浴中,在其中使膜、帶或單纖絲冷卻並固化。膜、帶或單纖絲可然後依次自水浴傳遞出並經受其他處理步驟。在自水浴浮現時,膜、帶或單纖絲可夾帶水,此干擾後續處理步驟。此自水浴夾帶水之效應在科技文獻中通常稱為「水騰帶(water carry-over)」,且其可縮寫為WCO。
在適宜溫度下拉伸膜導致聚合物定向及進一步結晶,從而產生特定性質。此第二處理步驟可直接在膜上進行,但在拉伸製程前通常將初級膜***成帶。由於期望性質係在拉伸製程期間獲得,因此在此精確遵從所有製程參數係至關重要的。即使在拉伸製程前在膜或帶上之痕量水分亦改變隨後的拉伸及定向,以致所獲得產物之品質方面產生極嚴重之變化。此效應超出僅僅所得最終產物品質之相應主要變化。即使在生產或處理期間,差的品質可引起例如帶之斷裂並由此停止生產。可導致所提及問題之水源係初級膜擠出至其中之冷水浴。雖然大多數塑膠、尤其聚烯烴(例如聚乙烯(PE)或聚丙烯(PP))極具疏水性且因此幾乎不具有吸收水之傾向,但經常發現在相對較高生產速度下,在將膜牽拉至水浴上方時,水滴或水之薄膜附著至膜。此外,需將諸如光安定劑之各種添加劑添加至聚合物以確保最終產物具有良好功能性。一些此等添加劑促使自水浴夾帶的水增加。若欲以低成本生產適宜產物,則添加劑以及最大處理速度係必需的。處理速度降低導致不經濟之生產。添加其中一些導致WCO變差(即,更多之WCO且因此更差之產品)之必要添加劑亦係不可避免的,此乃因否則不能達成由添加劑所帶來之產物性質。
當前WCO之降低係經由在機械製造期間簡單設計措施來促進。舉例而言,膜自水浴之抽出通常垂直向上,以使重力單獨地使得滴落離開的水之量最大。此外,通常使用擠壓輥及/或氣刀以自膜去除最大量之水。存在其他技術方法,此取決於機器之特定構形。
仍需要在聚烯烴膜、帶及單纖絲之生產期間改良WCO之方法。理想地,不應出現不期望之副作用,且該方法亦應能夠毫無問題的用於現有調配物。
令人驚訝地,現已發現將特定第二空間位阻胺光安定劑添加至已含有空間位阻胺光安定劑之經光安定化之聚烯烴膜、帶或單纖絲可在生產期間顯著降低WCO。此係意料之外的,特別是由於該兩種空間位阻胺係屬同一類化合物。完全令人意外且根本無法預測的是,兩種空間位阻胺光安定劑之具體組合顯示WCO性質之協同改良。
因此,本發明提供用於降低含有組份(A)作為光安定劑且在生產期間穿過水浴之經光安定化之聚烯烴膜(較佳單層)、帶(較佳單層)或單纖絲之水騰帶之方法,其特徵在於該聚烯烴膜、帶或單纖絲額外包含組份(B)作為光安定劑,
組份(A)係至少一種選自由式(A-I)化合物、式(A-II)化合物及式(A-III)化合物組成之群之化合物,
其中A1
係氫或C1
-C4
烷基,
A2
係直接鍵或C1
-C10
伸烷基,且
a1
係2至20之數值;
其中A3
、A4
及A5
彼此獨立地係C2
-C18
伸烷基,
A6
、A7
、A8
、A9
及A10
彼此獨立地係氫、C1
-C12
烷基、C5
-C12
環烷基或式(a-1)之基團,
基團A11
彼此獨立地係氫、C1
-C12
烷基或C5
-C12
環烷基,且
a2
係1至20之數值;
其中A12
係C2
-C18
伸烷基、C5
-C7
伸環烷基或C1
-C4
伸烷基二(C5
-C7
伸環烷基),
A13
及A14
彼此獨立地係氫、C1
-C12
烷基、C5
-C12
環烷基或式(a-2)之基團,
或基團A13
及A14
連同其所鍵結之氮原子一起形成5至10-員雜環,
基團A15
彼此獨立地係氫、C1
-C12
烷基或C5
-C12
環烷基,且
a3
係2至20之數值;
組份(B)係至少一種選自由式(B-I)化合物、式(B-II)化合物、式(B-III)化合物及式(B-IV)化合物組成之群之化合物,
其中R1
係C1
-C18
烷基、C1
-C18
羥基烷基、環己基或羥基環己基,或R1
係基團-C(C6
H5
)(H)CH2
-OH且R2
係C1
-C25
烷基或式(b-1)之基團;
其中x係2至8之整數且y係0或1;
其中R3
係C2
-C18
伸烷基、C5
-C7
伸環烷基或C1
-C4
伸烷基二(C5
-C7
伸環烷基),
基團R4
彼此獨立地係C1
-C12
烷基或C5
-C12
環烷基,
R5
及R6
彼此獨立地係氫、C1
-C12
烷基、C5
-C12
環烷基或式(b-2)之基團,
或基團R5
及R6
連同其所鍵結之氮原子一起形成5至10-員雜環且
b1
係1至20之數值;
其中基團R8
、R9
及R10
彼此獨立地係C2
-C18
伸烷基且基團R7
彼此獨立地係式(b-3)之基團
其中R11
及R12
彼此獨立地係氫、C1
-C12
烷基、C5
-C12
環烷基或式(b-4)之基團
且基團R13
彼此獨立地係C1
-C12
烷基或C5
-C12
環烷基;
其中
R5
係C1
-C25
烷基,
n係1至10之數值,且
W係包含介於50與1000個碳原子間之蠟殘基、較佳聚乙烯或聚丙烯蠟之殘基。
若膜係多層膜,則組份(A)及(B)較佳在一個層中。
組份(A)及(B)之化合物係已知的且大部分可商業購得,並且可根據已知方法製備。
組份(A)之化合物可(例如)以類似於US-A-4,233,412、US-A-4,477,615 (CAS 136,504-96-6)及US-A-4,108,829、US-A-4,086,204、US-A-4,331,586、US-A-6,046,304及US-A-6,297,299中所闡述之方法製備。
組份(B)之化合物可(例如)以類似於US-A-6,388,072、US-A-6,117,995、US-A-6,420,462及US-A-6,677,451及US-A-5,844,026中所述之方法製備。
組份(A)之較佳化合物係商業產品Tinuvin®
622、Sabostab®
UV
119、Uvasorb®
HA88、Uvasorb®
HA10、Chimassorb®
944、Chimassorb®
2020、Cyasorb®
UV 3346、Cyasorb®
UV 3529及Dastib®
1082。
組份(B)之較佳化合物係商業產品Tinuvin®
NOR 371、Tinuvin®
123、ADK STAB®
LA81或Flamestab®
NOR 116。
聚烯烴較佳係聚乙烯或聚丙烯,且含有(例如)相對於聚烯烴重量之0.01%至10%、尤其0.1%至1%組份(A)及(B)之總和。
組份(A)對組份(B)之重量比係(例如) 1:20至20:1、較佳地1:15至15:1。
使式(A-I)、(A-II)、(A-III)及(B-II)之化合物中自由價飽和之末端基團之意義取決於其製備方法。末端基團亦可在化合物製備之後經修飾。
若(例如)藉由使式之化合物(其中A1
係氫或甲基)與式Y0
-OOC-A2
-COO-Y0
之二羧酸二酯(其中Y0
係(例如)甲基、乙基或丙基,且A2
係如上文所定義)反應來製備式(A-I)化合物,則與2,2,6,6-四甲基-4-氧基六氫吡啶-1-基鍵結之末端基團係氫或-CO-A2
-COO-Y0
,且與二醯基鍵結之末端基團係-O-Y0
或。
在式(A-II)化合物中,與三嗪基團鍵結之末端基團係(例如) Cl或基團
且與胺基鍵結之末端基團係(例如)氫或基團。
若藉由使式化合物(其中X0
係(例如)鹵素、尤其氯,且A13
及A14
係如上文所定義)與式化合物(其中A12
及A15
係如上文所定義)反應來製備式(A-III)化合物,則與二胺基鍵結之末端基團係(例如)氫或
且與三嗪基團鍵結之末端基團係(例如) X0
或。
若X0
係鹵素,則當反應完成時,其有利地經(例如) -OH或胺基取代。可提及胺基之實例係吡咯啶-1-基、嗎啉基、-NH2
、-N((C1
-C8
)烷基)2
及-NR0
(C1
-C8
烷基),其中R0
係氫或式(a-2)之基團。
式(A-III)之尤其較佳化合物中之一者係
其中E1
係,E2
係且a3
係2至10之數值。
此化合物之製備闡述於US-A-6,046,304之實例10中。
在式(B-II)化合物中,與二胺基鍵結之端基係(例如)氫或
且與三嗪基團鍵結之末端基團係(例如)。
具有最多25個碳原子之烷基之實例係甲基、乙基、丙基、異丙基、正丁基、第二丁基、異丁基、第三丁基、2-乙基丁基、正戊基、異戊基、1-甲基戊基、1,3-二甲基丁基、正己基、1-甲基己基、正庚基、異庚基、1,1,3,3-四甲基丁基、1-甲基庚基、3-甲基庚基、正辛基、2-乙基己基、1,1,3-三甲基-己基、1,1,3,3-四甲基戊基、壬基、癸基、十一烷基、1-甲基十一烷基、十二烷基、1,1,3,3,5,5-六甲基己基、十三烷基、十四烷基、十五烷基、十六烷基、十七烷基及十八烷基。
C5
-C12
環烷基之實例係環戊基、環己基、環庚基、環辛基及環十二烷基。環己基係較佳的。
具有最多18個碳原子之伸烷基之實例係亞甲基、伸乙基、伸丙基、三亞甲基、四亞甲基、五亞甲基、2,2-二甲基三亞甲基、六亞甲基、十亞甲基及十八亞甲基。
C5
-C7
伸環烷基之較佳實例係伸環己基。
C1
-C4
伸烷基二(C5
-C7
伸環烷基)之較佳實例係伸環己基-亞甲基-伸環己基。
5至7-員雜環之較佳實例係嗎啉基。
在較佳方法中,A1
係氫,
A2
係C2
-C6
伸烷基,且
a1
係2至10之數值;
A3
、A4
及A5
彼此獨立地係C2
-C6
伸烷基,
A6
、A7
、A8
、A9
及A10
彼此獨立地係C1
-C4
烷基,
基團A11
彼此獨立地係氫或C1
-C4
烷基,且
a2
係1至10之數值;
A12
係C2
-C6
伸烷基,
A13
及A14
彼此獨立地係氫、C1
-C4
烷基、環己基或式(a-2)之基團,
或基團A13
及A14
連同其所鍵結之氮原子一起形成嗎啉基,
基團A15
彼此獨立地係氫或C1
-C4
烷基,且
a3
係2至10之數值,
R1
係C1
-C11
烷基或C2
-C6
羥基烷基,R2
係C10
-C20
烷基或式(b-1)之基團;
R3
係C2
-C6
伸烷基,
基團R4
彼此獨立地係C1
-C4
烷基或環己基;
R5
及R6
彼此獨立地係氫、C1
-C4
烷基、環己基或式(b-2)之基團,
或基團R5
及R6
連同其所鍵結之氮原子一起形成嗎啉基且
b1
係1至10之數值;
R8
、R9
及R10
彼此獨立地係C2
-C6
伸烷基且基團R7
彼此獨立地係式(b-3)之基團,
R11
及R12
彼此獨立地係C1
-C4
烷基,且基團R13
彼此獨立地係C1
-C4
烷基或環己基。
根據較佳實施例,式(A-I)化合物對應於式(A-I-1)
其中a1
係2至10之數值,
式(A-II)化合物對應於式(A-II-1)或(A-II-2),
其中a2
係1至10之數值,
其中a2
係1至10之數值,
式(A-III)化合物對應於式(A-III-1)、(A-III-2)、(A-III-3)或(A-III-4),
其中a3
係2至10之數值,
其中a3
係2至10之數值,
其中A15
係氫或甲基且a3
係2至10之數值,
其中a3
係2至10之數值。
式(B-I)化合物對應於式(B-I-1)、(B-I-2)或(B-I-3),
式(B-II)化合物對應於式(B-II-1),
其中b1
係1至10之數值,
式(B-III)化合物對應於式(B-III-1),
其中R7
係式(b-3-1)之基團。
根據尤其較佳實施例,組份(A)係式(A-I-1)化合物且組份(B)係式(B-II-1)化合物,或
組份(A)係式(A-II-1-a)化合物且組份(B)係式(B-III-1)化合物,或
組份(A)係式(A-III-2)化合物且組份(B)係式(B-I-1)化合物,
其中a1
係2至10之數值,
其中X係基團且
Y係基團,
其中a3
係2至10之數值,
其中b1
係1至10之數值,
其中R7
係式(b-3-1)之基團。
聚烯烴可額外含有一或多種習用添加劑。下文列出適宜實例。1. 抗氧化劑 1.1. 烷基化單酚
,例如2,6-二-第三丁基-4-甲基苯酚、2-第三丁基-4,6-二甲基苯酚、2,6-二-第三丁基-4-乙基苯酚、2,6-二-第三丁基-4-正丁基苯酚、2,6-二-第三丁基-4-異丁基苯酚、2,6-二環戊基-4-甲基苯酚、2-(α-甲基環己基)-4,6-二甲基苯酚、2,6-二-十八烷基-4-甲基苯酚、2,4,6-三環己基苯酚、2,6-二-第三丁基-4-甲氧基甲基苯酚、側鏈中為直鏈或具支鏈之壬基苯酚(例如2,6-二-壬基-4-甲基苯酚)、2,4-二甲基-6-(1’-甲基十一-1’-基)苯酚、2,4-二甲基-6-(1’-甲基十七-1’-基)苯酚、2,4-二甲基-6-(1’-甲基十三-1’-基)苯酚及其混合物。1.2. 烷基硫基甲基苯酚
,例如2,4-二辛基硫基甲基-6-第三丁基苯酚、2,4-二辛基硫基甲基-6-甲基苯酚、2,4-二辛基硫基甲基-6-乙基苯酚、2,6-二-十二烷基硫基甲基-4-壬基苯酚。1.3. 氫醌及烷基化氫醌
,例如2,6-二-第三丁基-4-甲氧基苯酚、2,5-二-第三丁基氫醌、2,5-二-第三戊基氫醌、2,6-二苯基-4-十八烷基氧基苯酚、2,6-二-第三丁基氫醌、2,5-二-第三丁基-4-羥基苯甲醚、3,5-二-第三丁基-4-羥基苯甲醚、硬脂酸3,5-二-第三丁基-4-羥基苯基酯、己二酸雙(3,5-二-第三丁基-4-羥基苯基)酯。1.4. 生育酚
,例如α-生育酚、β-生育酚、γ-生育酚、δ-生育酚及其混合物(維生素E)。1.5. 羥基化硫基二苯基醚
,例如2,2’-硫基雙(6-第三丁基-4-甲基苯酚)、2,2’-硫基雙(4-辛基苯酚)、4,4’-硫基雙(6-第三丁基-3-甲基苯酚)、4,4’-硫基雙(6-第三丁基-2-甲基苯酚)、4,4’-硫基雙(3,6-二-第二戊基苯酚)、4,4’-雙(2,6-二甲基-4-羥基苯基)二硫化物。1.6. 亞烷基雙酚
,例如2,2’-亞甲基雙(6-第三丁基-4-甲基苯酚)、2,2’-亞甲基雙(6-第三丁基-4-乙基苯酚)、2,2’-亞甲基雙[4-甲基-6-(α-甲基環己基)苯酚]、2,2’-亞甲基雙(4-甲基-6-環己基苯酚)、2,2’-亞甲基雙(6-壬基-4-甲基苯酚)、2,2’-亞甲基雙(4,6-二-第三丁基苯酚)、2,2’-亞乙基雙(4,6-二-第三丁基苯酚)、2,2’-亞乙基雙(6-第三丁基-4-異丁基苯酚)、2,2’-亞甲基雙[6-(α-甲基苄基)-4-壬基苯酚]、2,2’-亞甲基雙[6-(α,α-二甲基苄基)-4-壬基苯酚]、4,4’-亞甲基雙(2,6-二-第三丁基苯酚)、4,4’-亞甲基雙(6-第三丁基-2-甲基苯酚)、1,1-雙(5-第三丁基-4-羥基-2-甲基苯基)丁烷、2,6-雙(3-第三丁基-5-甲基-2-羥基苄基)-4-甲基苯酚、1,1,3-三(5-第三丁基-4-羥基-2-甲基苯基)丁烷、1,1-雙(5-第三丁基-4-羥基-2-甲基-苯基)-3-正十二烷基巰基丁烷、乙二醇雙[3,3-雙(3’-第三丁基-4’-羥基苯基)丁酸酯]、雙(3-第三丁基-4-羥基-5-甲基-苯基)二環戊二烯、對苯二甲酸雙[2-(3’-第三丁基-2’-羥基-5’-甲基苄基)-6-第三丁基-4-甲基苯基]酯、1,1-雙-(3,5-二甲基-2-羥基苯基)丁烷、2,2-雙(3,5-二-第三丁基-4-羥基苯基)丙烷、2,2-雙(5-第三丁基-4-羥基-2-甲基苯基)-4-正十二烷基巰基丁烷、1,1,5,5-四-(5-第三丁基-4-羥基-2-甲基苯基)戊烷。1.7. O- 、 N- 及 S- 苄基化合物
,例如3,5,3’,5’-四-第三丁基-4,4’-二羥基二苄基醚、4-羥基-3,5-二甲基苄基巰基乙酸十八烷基酯、4-羥基-3,5-二-第三丁基苄基巰基乙酸十三烷基酯、三(3,5-二-第三丁基-4-羥基苄基)胺、二硫代對苯二甲酸雙(4-第三丁基-3-羥基-2,6-二甲基苄基)酯、雙(3,5-二-第三丁基-4-羥基苄基)硫化物、3,5-二-第三丁基-4-羥基苄基巰基乙酸異辛基酯。1.8. 羥基苄基化丙二酸酯
,例如2,2-雙(3,5-二-第三丁基-2-羥基苄基)丙二酸二-十八烷基酯、2-(3-第三丁基-4-羥基-5-甲基苄基)丙二酸二-十八烷基酯、2,2-雙(3,5-二-第三丁基-4-羥基苄基)丙二酸二-十二烷基巰基乙基酯、2,2-雙(3,5-二-第三丁基-4-羥基苄基)丙二酸雙[4-(1,1,3,3-四甲基丁基)苯基]酯。1.9. 芳香族羥基苄基化合物
,例如1,3,5-三(3,5-二-第三丁基-4-羥基苄基)-2,4,6-三甲基苯、1,4-雙(3,5-二-第三丁基-4-羥基苄基)-2,3,5,6-四甲基苯、2,4,6-三(3,5-二-第三丁基-4-羥基苄基)苯酚。1.10. 三嗪化合物
,例如2,4-雙(辛基巰基)-6-(3,5-二-第三丁基-4-羥基苯胺基)-1,3,5-三嗪、2-辛基巰基-4,6-雙(3,5-二-第三丁基-4-羥基苯胺基)-1,3,5-三嗪、2-辛基巰基-4,6-雙(3,5-二-第三丁基-4-羥基苯氧基)-1,3,5-三嗪、2,4,6-三(3,5-二-第三丁基-4-羥基苯氧基)-1,2,3-三嗪、1,3,5-三(3,5-二-第三丁基-4-羥基苄基)異氰尿酸酯、1,3,5-三(4-第三丁基-3-羥基-2,6-二甲基苄基)異氰尿酸酯、2,4,6-三(3,5-二-第三丁基-4-羥基苯基乙基)-1,3,5-三嗪、1,3,5-三(3,5-二-第三丁基-4-羥基苯基丙醯基)-六氫-1,3,5-三嗪、1,3,5-三(3,5-二環己基-4-羥基苄基)異氰尿酸酯。1.11. 苄基膦酸酯
,例如2,5-二-第三丁基-4-羥基苄基膦酸二甲基酯、3,5-二-第三丁基-4-羥基苄基膦酸二乙基酯、3,5-二-第三丁基-4-羥基苄基膦酸二-十八烷基酯、5-第三丁基-4-羥基-3-甲基苄基膦酸二-十八烷基酯、3,5-二-第三丁基-4-羥基苄基膦酸之單乙酯之鈣鹽。1.12. 醯胺基苯酚
,例如4-羥基月桂醯苯胺、4-羥基硬脂醯苯胺、N-(3,5-二-第三丁基-4-羥基苯基)胺基甲酸辛基酯。1.13. β-(3,5- 二 - 第三丁基 -4- 羥基苯基 ) 丙酸與以下之一元醇或多元醇之酯
:例如甲醇、乙醇、正辛醇、異辛醇、十八醇、1,6-己二醇、1,9-壬二醇、乙二醇、1,2-丙二醇、新戊二醇、硫代二乙二醇、二乙二醇、三乙二醇、新戊四醇、三(羥基乙基)異氰尿酸酯、N,N’-雙(羥基乙基)草醯胺、3-硫雜十一醇、3-硫雜十五醇、三甲基己二醇、三羥甲基丙烷、4-羥基甲基-1-磷雜-2,6,7-三氧雜雙環[2.2.2]辛烷。1.14. β -(5- 第三丁基 -4- 羥基 -3- 甲基苯基 ) 丙酸與以下之一元醇或多元醇之酯
:例如甲醇、乙醇、正辛醇、異辛醇、十八醇、1,6-己二醇、1,9-壬二醇、乙二醇、1,2-丙二醇、新戊二醇、硫代二乙二醇、二乙二醇、三乙二醇、新戊四醇、三(羥基乙基)異氰尿酸酯、N,N’-雙(羥基乙基)草醯胺、3-硫雜十一醇、3-硫雜十五醇、三甲基己二醇、三羥甲基丙烷、4-羥基甲基-1-磷雜-2,6,7-三氧雜雙環[2.2.2]辛烷;3,9-雙[2-{3-(3-第三丁基-4-羥基-5-甲基苯基)丙醯基氧基}-1,1-二甲基乙基]-2,4,8,10-四氧雜螺[5.5]十一烷。1.15. β -(3,5- 二環己基 -4- 羥基苯基 ) 丙酸與以下之一元醇或多元醇之酯
:例如甲醇、乙醇、辛醇、十八醇、1,6-己二醇、1,9-壬二醇、乙二醇、1,2-丙二醇、新戊二醇、硫代二乙二醇、二乙二醇、三乙二醇、新戊四醇、三(羥基乙基)異氰尿酸酯、N,N’-雙(羥基乙基)草醯胺、3-硫雜十一醇、3-硫雜十五醇、三甲基己二醇、三羥甲基丙烷、4-羥基甲基-1-磷雜-2,6,7-三氧雜雙環[2.2.2]辛烷。1.16. 3,5- 二 - 第三丁基 -4- 羥基苯基乙酸與以下之一元醇或多元醇之酯
:例如甲醇、乙醇、辛醇、十八醇、1,6-己二醇、1,9-壬二醇、乙二醇、1,2-丙二醇、新戊二醇、硫代二乙二醇、二乙二醇、三乙二醇、新戊四醇、三(羥基乙基)異氰尿酸酯、N,N’-雙(羥基乙基)草醯胺、3-硫雜十一醇、3-硫雜十五醇、三甲基己二醇、三羥甲基丙烷、4-羥基甲基-1-磷雜-2,6,7-三氧雜雙環[2.2.2]辛烷。1.17. β -(3,5- 二 - 第三丁基 -4- 羥基苯基 ) 丙酸之醯胺
,例如N,N’-雙(3,5-二-第三丁基-4-羥基苯基丙醯基)六亞甲基二醯胺、N,N’-雙(3,5-二-第三丁基-4-羥基苯基丙醯基)三亞甲基二醯胺、N,N’-雙(3,5-二-第三丁基-4-羥基苯基丙醯基)醯肼、N,N’-雙[2-(3-[3,5-二-第三丁基-4-羥基苯基]丙醯基氧基)乙基]草醯胺(Naugard®
XL-1,由Uniroyal供應)。1.18. 抗壞血酸
(維生素C)1.19. 胺抗氧化劑
,例如N,N’-二-異丙基-對苯二胺、N,N’-二-第二丁基-對苯二胺、N,N’-雙(1,4-二甲基戊基)-對苯二胺、N,N’-雙(1-乙基-3-甲基戊基)-對苯二胺、N,N’-雙(1-甲基庚基)-對苯二胺、N,N’-二環己基-對苯二胺、N,N’-二苯基-對苯二胺、N,N’-雙(2-萘基)-對苯二胺、N-異丙基-N’-苯基-對苯二胺、N-(1,3-二甲基丁基)-N’-苯基-對苯二胺、N-(1-甲基庚基)-N’-苯基-對苯二胺、N-環己基-N’-苯基-對苯二胺、4-(對甲苯胺磺醯基)二苯基胺、N,N’-二甲基-N,N’-二-第二丁基-對苯二胺、二苯基胺、N-烯丙基二苯基胺、4-異丙氧基二苯基胺、N-苯基-1-萘基胺、N-(4-第三辛基苯基)-1-萘基胺、N-苯基-2-萘基胺、辛基化二苯基胺(例如對,對’-二-第三辛基二苯基胺)、4-正丁基胺基苯酚、4-丁醯基胺基苯酚、4-壬醯基胺基苯酚、4-十二醯基胺基苯酚、4-十八醯基胺基苯酚、雙(4-甲氧基苯基)胺、2,6-二-第三丁基-4-二甲基胺基甲基苯酚、2,4’-二胺基二苯基甲烷、4,4’-二胺基二苯基甲烷、N,N,N’,N’-四甲基-4,4’-二胺基二苯基甲烷、1,2-雙[(2-甲基苯基)胺基]乙烷、1,2-雙(苯基胺基)丙烷、(鄰甲苯基)雙胍、雙[4-(1’,3’-二甲基丁基)苯基]胺、第三辛基化N-苯基-1-萘基胺、單烷基化及二烷基化之第三丁基/第三辛基二苯基胺之混合物、單烷基化及二烷基化之壬基二苯基胺之混合物、單烷基化及二烷基化之十二烷基二苯基胺之混合物、單烷基化及二烷基化之異丙基/異己基二苯基胺之混合物、單烷基化及二烷基化之第三丁基二苯基胺之混合物、2,3-二氫-3,3-二甲基-4H-1,4-苯并噻嗪、啡噻嗪、單烷基化及二烷基化之第三丁基/第三辛基啡噻嗪之混合物、單烷基化及二烷基化之第三辛基-啡噻嗪之混合物、N-烯丙基啡噻嗪、N,N,N’,N’-四苯基-1,4-二胺基丁-2-烯。2. UV 吸收劑及光安定劑 2.1. 2-(2’- 羥基苯基 ) 苯并***
,例如2-(2’-羥基-5’-甲基苯基)-苯并***、2-(3’,5’-二-第三丁基-2’-羥基苯基)苯并***、2-(5’-第三丁基-2’-羥基苯基)苯并***、2-(2’-羥基-5’-(1,1,3,3-四甲基丁基)苯基)苯并***、2-(3’,5’-二-第三丁基-2’-羥基苯基)-5-氯-苯并***、2-(3’-第三丁基-2’-羥基-5’-甲基苯基)-5-氯-苯并***、2-(3’-第二丁基-5’-第三丁基-2’-羥基苯基)苯并***、2-(2’-羥基-4’-辛氧基苯基)苯并***、2-(3’,5’-二-第三戊基-2’-羥基苯基)苯并***、2-(3’,5’-雙-(α,α-二甲基苄基)-2’-羥基苯基)苯并***、2-(3’-第三丁基-2’-羥基-5’-(2-辛氧基羰基乙基)苯基)-5-氯-苯并***、2-(3’-第三丁基-5’-[2-(2-乙基己基氧基)-羰基乙基]-2’-羥基苯基)-5-氯-苯并***、2-(3’-第三丁基-2’-羥基-5’-(2-甲氧基羰基乙基)苯基)-5-氯-苯并***、2-(3’-第三-丁基-2’-羥基-5’-(2-甲氧基羰基乙基)苯基)苯并***、2-(3’-第三丁基-2’-羥基-5’-(2-辛氧基羰基乙基)苯基)苯并***、2-(3’-第三丁基-5’-[2-(2-乙基己基氧基)羰基乙基]-2’-羥基苯基)苯并***、2-(3’-十二烷基-2’-羥基-5’-甲基苯基)苯并***、2-(3’-第三丁基-2’-羥基-5’-(2-異辛基氧基羰基乙基)苯基苯并***、2,2’-亞甲基-雙[4-(1,1,3,3-四甲基丁基)-6-苯并***-2-基苯酚]、2-[3’-第三丁基-5’-(2-甲氧基羰基乙基)-2’-羥基苯基]-2H-苯并***與聚乙二醇300之轉酯化產物;,其中R = 3’-第三丁基-4’-羥基-5’-2H-苯并***-2-基苯基;2-[2’-羥基-3’-(α,α-二甲基苄基)-5’-(1,1,3,3-四甲基丁基)-苯基]苯并***、2-[2’-羥基-3’-(1,1,3,3-四甲基丁基)-5’-(α,α-二甲基苄基)-苯基]苯并***。2.2. 2- 羥基二苯基酮
,例如4-羥基、4-甲氧基、4-辛基氧基、4-癸基氧基、4-十二烷基氧基、4-苄氧基、4,2’,4’-三羥基及2’-羥基-4,4’-二甲氧基衍生物。2.3. 經取代及未經取代之苯甲酸之酯
,例如柳酸4-第三丁基-苯基酯、柳酸苯基酯、柳酸辛基苯基酯、二苯甲醯基間苯二酚、雙(4-第三丁基苯甲醯基)間苯二酚、苯甲醯基間苯二酚、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2-甲基-4,6-二-第三丁基苯基酯。2.4. 丙烯酸酯
,例如α-氰基-β,β-二苯基丙烯酸乙酯、α-氰基-β,β-二苯基丙烯酸異辛基酯、α-甲氧羰基肉桂酸甲酯、α-氰基-β-甲基-對甲氧基肉桂酸甲酯、α-氰基-β-甲基-對甲氧基-肉桂酸丁酯、α-甲氧羰基-對甲氧基肉桂酸甲酯、N-(β-甲氧羰基-β-氰基乙烯基)-2-甲基吲哚啉、四(α-氰基-β,β-二苯基丙烯酸)新戊基酯。2.5. 鎳化合物
,例如含或不含諸如正丁基胺、三乙醇胺或N-環己基二乙醇胺等額外配體之2,2’-硫基-雙[4-(1,1,3,3-四甲基丁基)苯酚]之鎳錯合物(例如1:1或1:2錯合物)、二丁基二硫基胺基甲酸鎳、單烷基酯(例如4-羥基-3,5-二-第三丁基苄基膦酸之甲酯或乙酯)之鎳鹽、酮肟(例如2-羥基-4-甲基苯基十一烷基酮肟)之鎳錯合物、含或不含額外配體之1-苯基-4-月桂醯基-5-羥基吡唑之鎳錯合物。2.6. 空間位阻胺
,例如碳酸雙(1-十一烷基氧基-2,2,6,6-四甲基-4-六氫吡啶基)酯、癸二酸雙(2,2,6,6-四甲基-4-六氫吡啶基)酯、琥珀酸雙(2,2,6,6-四甲基-4-六氫吡啶基)酯、癸二酸雙(1,2,2,6,6-五甲基-4-六氫吡啶基)酯、癸二酸雙(1-辛基氧基-2,2,6,6-四甲基-4-六氫吡啶基)酯、正丁基-3,5-二-第三丁基-4-羥基苄基丙二酸雙(1,2,2,6,6-五甲基-4-六氫吡啶基)酯、1-(2-羥基乙基)-2,2,6,6-四甲基-4-羥基六氫吡啶與琥珀酸之縮合物、N,N'-雙(2,2,6,6-四甲基-4-六氫吡啶基)六亞甲基二胺與4-第三辛基胺基-2,6-二氯-1,3,5-三嗪之直鏈或環狀縮合物、氮基三乙酸三(2,2,6,6-四甲基-4-六氫吡啶基)酯、1,2,3,4-丁烷四甲酸四(2,2,6,6-四甲基-4-六氫吡啶基)酯、1,1'-(1,2-乙二基)-雙(3,3,5,5-四甲基六氫吡嗪酮)、4-苯甲醯基-2,2,6,6-四甲基六氫吡啶、4-硬脂醯基氧基-2,2,6,6-四甲基六氫吡啶、2-正丁基-2-(2-羥基-3,5-二-第三丁基苄基)丙二酸雙(1,2,2,6,6-五甲基六氫吡啶基)酯、3-正辛基-7,7,9,9-四甲基-1,3,8-三氮雜螺[4.5]癸烷-2,4-二酮、癸二酸雙(1-辛基氧基-2,2,6,6-四甲基六氫吡啶基)酯、琥珀酸雙(1-辛基氧基-2,2,6,6-四甲基六氫吡啶基)酯、N,N'-雙(2,2,6,6-四甲基-4-六氫吡啶基)六亞甲基二胺與4-嗎啉基-2,6-二氯-1,3,5-三嗪之直鏈或環狀縮合物、2-氯-4,6-雙(4-正丁基胺基-2,2,6,6-四甲基六氫吡啶基)-1,3,5-三嗪與1,2-雙(3-胺基丙基胺基)乙烷之縮合物、2-氯-4,6-二-(4-正丁基胺基-1,2,2,6,6-五甲基六氫吡啶基)-1,3,5-三嗪與1,2-雙(3-胺基丙基胺基)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-4-六氫吡啶基)吡咯啶-2,5-二酮、3-十二烷基-1-(1,2,2,6,6-五甲基-4-六氫吡啶基)吡咯啶-2,5-二酮、4-十六烷基氧基-2,2,6,6-四甲基六氫吡啶與4-硬脂醯基氧基-2,2,6,6-四甲基六氫吡啶之混合物、N,N'-雙(2,2,6,6-四甲基-4-六氫吡啶基)六亞甲基二胺與4-環己基胺基-2,6-二氯-1,3,5-三嗪之縮合物、1,2-雙(3-胺基丙基胺基)乙烷與2,4,6-三氯-1,3,5-三嗪以及4-丁基胺基-2,2,6,6-四甲基六氫吡啶(CAS登記號[136504-96-6])之縮合物、1,6-己烷二胺與2,4,6-三氯-1,3,5-三嗪以及N,N-二丁胺及4-丁基胺基-2,2,6,6-四甲基六氫吡啶(CAS登記號[192268-64-7])之縮合物、N-(2,2,6,6-四甲基-4-六氫吡啶基)-正十二烷基琥珀醯亞胺、N-(1,2,2,6,6-五甲基-4-六氫吡啶基)-正十二烷基琥珀醯亞胺、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、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]癸烷與環氧氯丙烷之反應產物、1,1-雙(1,2,2,6,6-五甲基-4-六氫吡啶基氧基羰基)-2-(4-甲氧基苯基)乙烯、N,N'-雙-甲醯基-N,N'-雙(2,2,6,6-四甲基-4-六氫吡啶基)六亞甲基二胺、4-甲氧基亞甲基丙二酸與1,2,2,6,6-五甲基-4-羥基六氫吡啶之二酯、聚[甲基丙基-3-氧基-4-(2,2,6,6-四甲基-4-六氫吡啶基)]矽氧烷、馬來酸酐-α-烯烴共聚物與2,2,6,6-四甲基-4-胺基六氫吡啶或1,2,2,6,6-五甲基-4-胺基六氫吡啶之反應產物、2,4-雙[N-(1-環己基氧基-2,2,6,6-四甲基六氫吡啶-4-基)-正丁基胺基]-6-(2-羥基乙基)胺基-1,3,5-三嗪、1-(2-羥基-2-甲基丙氧基)-4-十八醯基氧基-2,2,6,6-四甲基六氫吡啶、5-(2-乙基己醯基)氧基甲基-3,3,5-三甲基-2-嗎啉酮、Sanduvor (Clariant; CAS登記號106917-31-1)、5-(2-乙基己醯基)氧基甲基-3,3,5-三甲基-2-嗎啉酮、2,4-雙[(1-環己基氧基-2,2,6,6-六氫吡啶-4-基)丁基胺基]-6-氯-均三嗪與N,N’-雙(3-胺基丙基)乙二胺之反應產物、1,3,5-三(N-環己基-N-(2,2,6,6-四甲基六氫吡嗪-3-酮-4-基)胺基)-均三嗪、1,3,5-三(N-環己基-N-(1,2,2,6,6-五甲基六氫吡嗪-3-酮-4-基)胺基)-均三嗪。2.7. 草醯胺
,例如4,4’-二辛基氧基草醯替苯胺、2,2’-二乙氧基草醯替苯胺、2,2’-二辛基氧基-5,5’-二-第三丁基草醯替苯胺、2,2’-二-十二烷基氧基-5,5’-二-第三丁基草醯替苯胺、2-乙氧基-2’-乙基草醯替苯胺、N,N’-雙(3-二甲基胺基丙基)草醯胺、2-乙氧基-5-第三丁基-2’-乙基草醯替苯胺及其與2-乙氧基-2’-乙基-5,4’-二-第三丁基草醯替苯胺之混合物、鄰-與對-甲氧基二取代之草醯替苯胺之混合物及鄰-與對-乙氧基二取代之草醯替苯胺之混合物。2.8. 2-(2- 羥基苯基 )-1,3,5- 三嗪
,例如2,4,6-三(2-羥基-4-辛基氧基苯基)-1,3,5-三嗪、2-(2-羥基-4-辛基氧基苯基)-4,6-雙(2,4-二甲基苯基)-1,3,5-三嗪、2-(2,4-二羥基苯基)-4,6-雙(2,4-二甲基苯基)-1,3,5-三嗪、2,4-雙(2-羥基-4-丙基氧基苯基)-6-(2,4-二甲基苯基)-1,3,5-三嗪、2-(2-羥基-4-辛基氧基苯基)-4,6-雙(4-甲基苯基)-1,3,5-三嗪、2-(2-羥基-4-十二烷基氧基苯基)-4,6-雙(2,4-二甲基苯基)-1,3,5-三嗪、2-(2-羥基-4-十三烷基氧基苯基)-4,6-雙(2,4-二甲基苯基)-1,3,5-三嗪、2-[2-羥基-4-(2-羥基-3-丁基氧基丙氧基)苯基]-4,6-雙(2,4-二甲基)-1,3,5-三嗪、2-[2-羥基-4-(2-羥基-3-辛基氧基丙基氧基)苯基]-4,6-雙(2,4-二甲基)-1,3,5-三嗪、2-[4-(十二烷基氧基/十三烷基氧基-2-羥基丙氧基)-2-羥基苯基]-4,6-雙(2,4-二甲基苯基)-1,3,5-三嗪、2-[2-羥基-4-(2-羥基-3-十二烷基氧基丙氧基)苯基]-4,6-雙(2,4-二甲基苯基)-1,3,5-三嗪、2-(2-羥基-4-己基氧基)苯基-4,6-二苯基-1,3,5-三嗪、2-(2-羥基-4-甲氧基苯基)-4,6-二苯基-1,3,5-三嗪、2,4,6-三[2-羥基-4-(3-丁氧基-2-羥基丙氧基)苯基]-1,3,5-三嗪、2-(2-羥基苯基)-4-(4-甲氧基苯基)-6-苯基-1,3,5-三嗪、2-{2-羥基-4-[3-(2-乙基己基-1-氧基)-2-羥基丙基氧基]苯基}-4,6-雙(2,4-二甲基苯基)-1,3,5-三嗪、2,4-雙(4-[2-乙基己基氧基]-2-羥基苯基)-6-(4-甲氧基苯基)-1,3,5-三嗪、2-(4,6-雙-聯苯-4-基-1,3,5-三嗪-2-基)-5-(2-乙基-(正)己基氧基)苯酚。3. 金屬去活化劑
,例如N,N’-二苯基草醯胺、N-柳醛-N’-柳醯基肼、N,N’-雙(柳醯基)肼、N,N’-雙(3,5-二-第三丁基-4-羥基苯基丙醯基)肼、3-柳醯基胺基-1,2,4-***、雙(亞苄基)草醯基二醯肼、草醯替苯胺、間苯二甲醯基二醯肼、癸二醯基雙苯基醯肼、N,N’-二乙醯基已二醯基二醯肼、N,N’-雙(柳醯基)草醯基二醯肼、N,N’-雙(柳醯基)硫代丙醯基二醯肼。4. 亞磷酸酯及亞膦酸酯
,例如亞磷酸三苯基酯、亞磷酸二苯基酯烷基酯、亞磷酸苯基酯二烷基酯、亞磷酸三(壬基苯基)酯、亞磷酸三月桂基酯、亞磷酸三-十八烷基酯、二硬脂醯基新戊四醇二亞磷酸酯、亞磷酸三(2,4-二-第三丁基苯基)酯、二異癸基新戊四醇二亞磷酸酯、雙(2,4-二-第三丁基苯基)新戊四醇二亞磷酸酯、雙(2,4-二-異丙苯基苯基)新戊四醇二亞磷酸酯、雙(2,6-二-第三丁基-4-甲基苯基)新戊四醇二亞磷酸酯、二異癸基氧基新戊四醇二亞磷酸酯、雙(2,4-二-第三丁基-6-甲基苯基)新戊四醇二亞磷酸酯、雙(2,4,6-三(第三丁基苯基))新戊四醇二亞磷酸酯、三硬脂醯基山梨糖醇三亞磷酸酯、4,4’-亞聯苯基二亞膦酸四(2,4-二-第三丁基苯基)酯、6-異辛基氧基-2,4,8,10-四-第三丁基-12H-二苯并[d,g]-1,3,2-二氧雜磷雜環辛烯(phosphocin)、亞磷酸雙(2,4-二-第三丁基-6-甲基苯基)甲基酯、亞磷酸雙(2,4-二-第三丁基-6-甲基苯基)乙基酯、6-氟-2,4,8,10-四-第三丁基-12-甲基-二苯并[d,g]-1,3,2-二氧雜磷雜環辛烯、2,2’,2’’-氮基[亞磷酸三乙基酯三(3,3’,5,5’-四-第三丁基-1,1’-聯苯-2,2’-二基)酯]、(3,3’,5,5’-四-第三丁基-1,1’-聯苯-2,2’-二基)亞磷酸2-乙基己基酯、5-丁基-5-乙基-2-(2,4,6-三-第三丁基苯氧基)-1,3,2-二氧雜磷雜環丙烷(phosphirane)。
以下亞磷酸酯尤佳:
亞磷酸三(2,4-二-第三丁基苯基)酯(Irgafos®
168,Ciba Specialty Chemicals公司)、亞磷酸三(壬基苯基)酯、 5. 羥基胺
,例如N,N-二苄基羥基胺、N,N-二乙基羥基胺、N,N-二辛基羥基胺、N,N-二月桂基羥基胺、N,N-二-十四烷基羥基胺、N,N-二-十六烷基羥基胺、N,N-二-十八烷基羥基胺、N-十六烷基-N-十八烷基羥基胺、N-十七烷基-N-十八烷基羥基胺、自氫化牛脂胺衍生之N,N-二烷基羥基胺。6. 硝酮
,例如N-苄基-α-苯基硝酮、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、自衍生自氫化牛脂胺之N,N-二烷基羥基胺衍生之硝酮。7. 硫增效劑
,例如硫代二丙酸二月桂基酯、硫代二丙酸二肉豆蔻基酯、硫代二丙酸二硬脂醯基酯、新戊四醇四[3-(十二烷基硫基)丙酸酯]或二硬脂醯基二硫化物。8. 過氧化物捕獲劑
,例如β-硫基二丙酸之酯,例如,月桂基、硬脂醯基、肉豆蔻基或十三烷基酯;巰基苯并咪唑或2-巰基苯并咪唑之鋅鹽、二丁基二硫基胺基甲酸鋅、二-十八烷基二硫化物、新戊四醇四(β-十二烷基巰基)丙酸酯。9. 聚醯胺安定劑
,例如銅鹽與碘化物及/或磷化合物之組合及二價錳之鹽。10. 鹼性共安定劑
,例如三聚氰胺、聚乙烯吡咯啶酮、二氰二胺、氰尿酸三烯丙酯、脲衍生物、肼衍生物、胺、聚醯胺、聚胺基甲酸酯、高級脂肪酸之鹼金屬鹽及鹼土金屬鹽,例如硬脂酸鈣、硬脂酸鋅、二十二酸鎂、硬脂酸鎂、蓖麻酸鈉及棕櫚酸鉀、焦兒茶酚銻或焦兒茶酚鋅。11. 成核劑
,例如無機物質,例如滑石、金屬氧化物(例如二氧化鈦或氧化鎂)、較佳鹼土金屬之磷酸鹽、碳酸鹽或硫酸鹽;有機化合物,例如單羧酸或多羧酸及其鹽,例如4-第三丁基苯甲酸、己二酸、二苯基乙酸、琥珀酸鈉或苯甲酸鈉;聚合化合物,例如離子型共聚物(離聚物)。尤佳者係1,3:2,4-雙(3’,4’-二甲基亞苄基)山梨糖醇、1,3:2,4-二(對甲基二亞苄基)山梨糖醇及1,3:2,4-二(亞苄基)山梨糖醇。12. 填充劑及強化劑
,例如碳酸鈣、矽酸鹽、玻璃纖維、玻璃珠、石棉、滑石、高嶺土(kaolin)、雲母、硫酸鋇、金屬氧化物及氫氧化物、碳黑、石墨、木粉及其他天然產物之粉狀物或纖維、合成纖維。13. 其他添加劑
,例如塑化劑、潤滑劑、乳化劑、顏料、流變添加劑、觸媒、流動控制劑、光學增白劑、阻燃劑、抗靜電劑及發泡劑。14. 苯并呋喃酮及吲哚啉酮
,例如彼等於U.S. 4,325,863;U.S. 4,338,244;U.S. 5,175,312;U.S. 5,216,052;U.S. 5,252,643;DE-A-4316611;DE-A-4316622;DE-A-4316876;EP-A-0589839;EP-A-0591102;EP-A-1291384中所揭示者或3-[4-(2-乙醯氧基乙氧基)苯基]-5,7-二-第三丁基苯并呋喃-2-酮、5,7-二-第三丁基-3-[4-(2-硬脂醯基氧基乙氧基)苯基]苯并呋喃-2-酮、3,3’-雙[5,7-二-第三丁基-3-(4-[2-羥基乙氧基]苯基)苯并呋喃-2-酮]、5,7-二-第三丁基-3-(4-乙氧基苯基)苯并呋喃-2-酮、3-(4-乙醯氧基-3,5-二甲基苯基)-5,7-二-第三丁基苯并呋喃-2-酮、3-(3,5-二甲基-4-新戊醯基氧基苯基)-5,7-二-第三丁基苯并呋喃-2-酮、3-(3,4-二甲基苯基)-5,7-二-第三丁基苯并呋喃-2-酮、3-(2,3-二甲基苯基)-5,7-二-第三丁基苯并呋喃-2-酮、3-(2-乙醯基-5-異辛基苯基)-5-異辛基苯并呋喃-2-酮。
組份(A)對習用添加劑之重量比係(例如) 1:100至100:1、較佳地1:100至10:1、尤其1:10至10:1。
根據較佳實施例,聚烯烴額外含有作為組份(C)之酚系抗氧化劑、較佳3-(3,5-二-第三丁基-4-羥基苯基)丙酸十八烷基酯。
組份(C)可以相對於聚烯烴重量之(例如) 0.01%至10%之濃度存在。
根據另一較佳實施例,組份(A)係式(A-I-1)化合物及式(A-III-2)化合物,且組份(B)係式(B-I-1)或(B-II-1)之化合物,且聚烯烴視情況包含3-(3,5-二-第三丁基-4-羥基苯基)丙酸十八烷基酯。
本發明之進一步實施例係根據上文所述方法製造之聚烯烴膜、帶或單纖絲。
本發明之另一實施例係使用組份(B)作為光安定劑以降低含有組份(A)作為光安定劑且在生產期間穿過水浴之經光安定化之聚烯烴膜、帶或單纖絲之水騰帶。
本發明之又另一實施例係製備經光安定化之聚烯烴膜、帶或單纖絲之方法,其包含使該經光安定化之聚烯烴膜、帶或單纖絲以5 m/min至100 m/min、較佳地4 m/min至80 m/min或10 m/min至50 m/min、尤其20 m/min至40 m/min之牽引速度穿過水浴之步驟,其特徵在於該聚烯烴膜、帶或單纖絲含有如上文所定義之組份(A)及(B)。上文所闡述之所有優選項均亦係關於此方法,該方法可用於降低水自水浴之騰帶。
以下之實例更詳細地說明本發明。除非另有說明,否則所有百分比及份數均係以重量計。在以下實例中所使用之安定劑: 化合物 (A-I-1) :
(Tinuvin®
622)
其中a1
係2至10之數值。化合物 (A-II-1-a) :
(Sabostab®
UV
119)
其中X係基團且
Y係基團。化合物 (A-III-2) :
(Chimassorb®
2020)
其中E1
係,E2
係且a3
係2至10之數值。化合物 (B-I-1) : 化合物 (B-II-1) :
其中E3
係,E4
係且其中b1
係2至10之數值。化合物 (B-III-1) :
(Flamestab®
NOR 116)
其中R7
係式之基團。下文所示試驗之協同作用之測定:
兩種光安定劑(α)及(β)之協同WCO (水騰帶)效應係藉由比較WCO之預期值與WCO活性之實際量測
值來測定。對於1:1比率之兩種光安定劑,預期值係基於相加定律(B. Ranby及J.F. Rabek; Photodegradation, Photo-oxidation and Photostabilization of Polymers, Principles and Applications, John Wiley & Sons, London, New York, Sydney, Toronto, 1975, 418及419頁)根據以下等式進行計算:
在下文實例中,當「所量測WCO」<
「所計算WCO」(低WCO值係期望的)時,兩種光安定劑存在協同WCO效應。
當兩種光安定劑之比率不為1:1時,可以適當方式修改以上等式;舉例而言,若比率為2:1,則可根據以下等式計算所預期WCO效應: 實例 1 :
將表1a及1b中所示之光安定劑在高速混合機(MTI, Mischtechnik International, Germany)中與聚乙烯(Dowlex®
SC 2108)混合。將混合物在雙螺桿擠出機(Krauss Maffei Berstorff, Germany)中於200℃下擠出以獲得顆粒,隨後將其在半工業帶生產線(Leonard, Italy)中於220℃下轉換為帶。水騰帶係表示為在進入拉伸部件之前來自水冷卻浴之水與擠出物(200微米)一起運送之長度(mm)。水騰帶越低,則可越快及越經濟地處理膜、拉伸帶或單纖絲。結果係顯示於表1a及1b中。表 1a :
*)低值係期望的。表 1b :
*)低值係期望的。實例 2 :
將表2a及2b中所示之光安定劑在高速混合機(MTI, Mischtechnik International, Germany)中與聚乙烯(Dowlex®
SC 2108)混合,該聚乙烯含有相對於聚乙烯重量之0.5重量%之化合物(A-I-1)。將混合物在雙螺桿擠出機(Krauss Maffei Berstorff, Germany)中於200℃下擠出以獲得顆粒,隨後將其在半工業帶生產線(Leonard, Italy)中於220℃下轉換為帶。水騰帶係表示為在進入拉伸部件之前來自水冷卻浴之水與擠出物(200微米)一起運送之長度(mm)。水騰帶越低,則可越快及越經濟地處理膜、拉伸帶或單纖絲。結果係顯示於表2a及2b中。表 2a :
*)低值係期望的。表 2b :
*)低值係期望的。實例 3 :
將表3a及3b中所示之光安定劑在高速混合機(MTI, Mischtechnik International, Germany)中與聚丙烯(Polychim®
A 10 TB)混合。將混合物在雙螺桿擠出機(Krauss Maffei Berstorff, Germany)中於230℃下擠出以獲得顆粒,隨後將其在半工業帶生產線(Leonard, Italy)中於240℃下轉換為帶。水騰帶係表示為在進入拉伸部件之前來自水冷卻浴之水與擠出物(240微米)一起運送之長度(mm)。水騰帶越低,則可越快及越經濟地處理膜、拉伸帶或單纖絲。結果係顯示於表3a及3b中。表 3a :
*)低值係期望的。表 3b :
*)低值係期望的。實例 4 :
將表4中所示之光安定劑在高速混合機(MTI, Mischtechnik International, Germany)中與聚乙烯(Dowlex®
SC 2108)混合,該聚乙烯含有相對於聚乙烯重量之0.5重量%之化合物(A-I-1)。將混合物在雙螺桿擠出機(Krauss Maffei Berstorff, Germany)中於200℃下擠出以獲得顆粒,隨後將其在半工業帶生產線(Leonard, Italy)中於220℃下轉換為帶。水騰帶係表示為在進入拉伸部件之前來自水冷卻浴之水與擠出物(100微米)一起運送之長度(mm)。水騰帶越低,則可越快及越經濟地處理膜、拉伸帶或單纖絲。結果係顯示於表4中。表 4 :
*)低值係期望的。
在以上實例中,「%」意指「相對於聚烯烴重量以重量計之%」。
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