JPS6317944A - Polyolefin composition - Google Patents

Polyolefin composition

Info

Publication number
JPS6317944A
JPS6317944A JP16083686A JP16083686A JPS6317944A JP S6317944 A JPS6317944 A JP S6317944A JP 16083686 A JP16083686 A JP 16083686A JP 16083686 A JP16083686 A JP 16083686A JP S6317944 A JPS6317944 A JP S6317944A
Authority
JP
Japan
Prior art keywords
polyolefin
formula
tert
tetrakis
bis
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.)
Granted
Application number
JP16083686A
Other languages
Japanese (ja)
Other versions
JPH0762094B2 (en
Inventor
Satoru Nagami
哲 永見
Keiji Kawamoto
圭司 河本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsui Petrochemical Industries Ltd
Original Assignee
Mitsui Petrochemical Industries Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsui Petrochemical Industries Ltd filed Critical Mitsui Petrochemical Industries Ltd
Priority to JP61160836A priority Critical patent/JPH0762094B2/en
Publication of JPS6317944A publication Critical patent/JPS6317944A/en
Publication of JPH0762094B2 publication Critical patent/JPH0762094B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:A polyolefin composition having good heat resistance and weather resistance and improved discoloration in pink, obtained by blending polyolefin with specific two compounds and a specified phosphorus weather-resistant stabilizer. CONSTITUTION:100pts.wt. polyolefin is blended with (A) tetrakis[methylene-3-(3,5- di-t-butyl-4-hydroxyphenyl)propionate]methane, such as 0.03-0.3pt.wt. compound shown by formula I, (B) bis(2,2',6,6'-tetraalkyl-4-piperidine)dicarboxylate, such as 0.05-0.4pt.wt. compound shown by formula II and (C) one or more phosphorus type stabilizer of hydrogenated bisphenol type-pentaerythritol phosphite polymer, di-10-20C alkylpentaerythritol diphosphite, etc., such as compounds shown by formula III formula IV in an amount to give 50-500wt% based on total amounts of the components A and B and the aimed composition is obtained.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は耐熱性、耐候性を有し、かつピンク変色の改善
されたポリオレフィン組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a polyolefin composition having heat resistance, weather resistance, and improved pink discoloration.

従来の技術 ポリオレフィンの主要な用途の一つとして自動車の内外
装板が挙げられるが、この場合の要求される性質として
耐熱性と耐候性がある。
Background Art One of the main uses of polyolefins is the interior and exterior panels of automobiles, and the required properties in this case are heat resistance and weather resistance.

この要求に対し従来はポリオレフィンにIrganox
lolo(チバ書ガイギー社の商品名)やサノールLS
770  (ピペラジン系耐候安定剤、三共製)などの
添加剤を配合する処決は良く知られている。
To meet this demand, conventional polyolefins such as Irganox
lolo (product name of Ciba Sho Geigy) and Sanol LS
770 (piperazine weathering stabilizer, manufactured by Sankyo) is a well-known solution.

発明が解決しようとする問題点 前記ポリオレフィン組成物が自動車の内外装板に使用さ
れると、燃焼誹ガス、原動機排ガス等に存在するNOx
に起因すると思われるピンクに変色する欠点を有してい
る。
Problems to be Solved by the Invention When the polyolefin composition is used for the interior and exterior panels of automobiles, NOx present in combustion gas, motor exhaust gas, etc.
It has the disadvantage of turning pink, which is thought to be caused by.

本発明はこのピンク変色を改善することを目的とする。The present invention aims to improve this pink discoloration.

問題点を解決するための手段 本発明は、ポリオレフィンに次の化合物を配合したこと
を特徴とする耐熱性及び耐候性にすぐれたポリオレフィ
ン組成物である。
Means for Solving the Problems The present invention is a polyolefin composition with excellent heat resistance and weather resistance, which is characterized by blending the following compounds into a polyolefin.

(1)テトラキス〔メチレン−3−(3,5−ジ−te
rt−ブチルー4−ヒドロキシフェニル)プロピオネー
トコメタン(以下化合物Aと云う)(2)ビス(2,2
′、6.6’−テトラアルキル−4−ピペリジン)ジカ
ルボキシレート(以下化合物Bと云う) (3)次の[1]〜[4]で示されるリン系安定剤の1
種又は2種以上。
(1) Tetrakis [methylene-3-(3,5-di-te)
rt-butyl-4-hydroxyphenyl)propionate comethane (hereinafter referred to as compound A) (2) bis(2,2
', 6.6'-tetraalkyl-4-piperidine) dicarboxylate (hereinafter referred to as compound B) (3) 1 of the phosphorus stabilizers shown in the following [1] to [4]
A species or two or more species.

[1]テトラキス−(2−tert−アルキル又は2.
4−ジ−tert−アルキルフェニル)一又は4,4′
−ビアリーレンジホスボナイト(以下化合物Cと云う) ■水素添加ビスフェノール系−ペンタエリスリトールホ
スファイトポリマー(以下化合物りと云う) ■ジC□。〜C2゜アルキルペンタエリスリトールシフ
オスファイト(以下化合物Eと云う)■ビス(2−te
rt又は2,4−ジ−tert−フルキルフェニル)ペ
ンタエリスリトールジホスファイト (以下化合物Fと
云う) 本発明でいうポリオレフィン組成物の基材ポリオレフィ
ンは代表的にはポリエチレン、ポリプロピレン、4−メ
チル−1−ペンテンの単独重合体又は共重合体、(TP
X■)等の高結晶質成分、エチレン−α−オレフィン非
晶質又は低結晶質重合体、プロピレン−1−ブテンの低
結晶質又は非結晶質共重体等の低結晶質又は非晶質成分
などのブロック共重合体又はブレンドである。
[1] Tetrakis-(2-tert-alkyl or 2.
4-di-tert-alkylphenyl)-1 or 4,4'
- Biarylene diphosbonite (hereinafter referred to as compound C) ■Hydrogenated bisphenol-based pentaerythritol phosphite polymer (hereinafter referred to as compound Rito) ■DiC□. ~C2゜Alkylpentaerythritol siphosphite (hereinafter referred to as compound E) ■Bis(2-te
rt or 2,4-di-tert-furkylphenyl) pentaerythritol diphosphite (hereinafter referred to as compound F) The base polyolefin of the polyolefin composition in the present invention is typically polyethylene, polypropylene, 4-methyl- Homopolymer or copolymer of 1-pentene, (TP
Highly crystalline components such as block copolymers or blends such as

・これらに要求される代表的な物性値としては、MFR
(230℃) 5〜30g/10m1n 、好ましくは
8〜15g/10m1n 。
・The typical physical property values required for these are MFR
(230°C) 5 to 30 g/10 m1n, preferably 8 to 15 g/10 m1n.

を挙げることができ、他の物性は用途に応じて定められ
る。
Other physical properties are determined depending on the application.

化合物Aの代表例としてはIrganoxlOlo(チ
バ・ガイギー社)の商品名で知られ、次の構造式を有し
ている。この化合物Aをポリオレフィン100重量部に
対して0.03〜0.3重量部を使用す・る、その使用
量が下限未満では耐酸化性付与能力が不足し、上限超で
は、配合物のピンク変色が明らかに(三共製)で知られ
、次の構造式を有している。
A representative example of Compound A is known under the trade name IrganoxlOlo (Ciba Geigy) and has the following structural formula. Compound A is used in an amount of 0.03 to 0.3 parts by weight per 100 parts by weight of the polyolefin.If the amount used is less than the lower limit, the ability to impart oxidation resistance will be insufficient, and if it exceeds the upper limit, the composition will become pink. It is known for its color change (manufactured by Sankyo) and has the following structural formula.

この化合物Bをポリオレフィン100重量部に対して通
常0.05〜0.4重量部を使用する。その使用量が下
限未満では配合物に耐候性を付与する能力に不足を来し
、上限超では、化合物Bのブルーミングを生ずる。
This compound B is usually used in an amount of 0.05 to 0.4 parts by weight per 100 parts by weight of the polyolefin. If the amount used is less than the lower limit, the ability to impart weather resistance to the formulation will be insufficient, and if it is more than the upper limit, blooming of compound B will occur.

ピンク変色防止のために用いるリン系耐候安定剤の代表
例(化合物C,D、E、F)は次の構造式〇〜■で示さ
れるリン酸系化合物又は亜リン酸系化合物である。
Representative examples of phosphorus-based weathering stabilizers (compounds C, D, E, and F) used to prevent pink discoloration are phosphoric acid-based compounds or phosphorous acid-based compounds represented by the following structural formulas 〇-■.

■テトラキス(2,4−ジ−tert−ブチルフェニル
)−4,4”−ビフェニレンジホスホナイト商品名P−
EPQ(サンド社製)として市販されている。
■Tetrakis(2,4-di-tert-butylphenyl)-4,4”-biphenylene diphosphonite Product name P-
It is commercially available as EPQ (manufactured by Sandoz Co.).

■水素添加ビスフェノールA−ペンタエリスリトールホ
スファイトポリマー いる。
■Hydrogenated bisphenol A-pentaerythritol phosphite polymer.

■ジステアリルベンタエリスリトールジホスファ商品名
ウニストン618(Weston818 、ポルグワー
ナー社製)として市販されている。
■ Distearylbentaerythritol diphospha is commercially available under the trade name of Weston 618 (manufactured by Porg Warner).

■ビス(2,4−ジ−t−ブチルフェニル)ペン商品名
ウニストン824(Weston824 、ポルグワー
ナー社製)として市販されている。
(2) Bis(2,4-di-t-butylphenyl) pen Commercially available under the trade name Weston 824 (manufactured by Porg Warner).

これらを1種又は2種以上用い、使用量は化合物A及び
化合物Bの合計量に対して50〜500%程度である。
One or more of these are used, and the amount used is about 50 to 500% of the total amount of compound A and compound B.

実施例 以下実施例を用いて説明する。Example This will be explained below using examples.

ポリオレフ4ン(MFR(230℃) 10g/10m
+1n)100重量部に対し第1表に示す処方で試験片
を成形し、倉庫内にNOxガスを高濃度に含む空気雰囲
気下12か月間保管し、試験片のピンク変色を目視及び
a値測定によって評価した。
Polyolefin 4 (MFR (230℃) 10g/10m
+1n) Form a test piece using the formulation shown in Table 1 for 100 parts by weight, store it in a warehouse for 12 months in an air atmosphere containing a high concentration of NOx gas, and visually check the pink discoloration of the test piece and measure the a value. Evaluated by.

a値とは、JIS 28730−1980 (ハンター
色差表示法)によるもので、JIS 8722に規定す
る三刺激値x、y、zより次の式 %式% で表わされるクロマティクネス指数を求めたものである
The a value is based on JIS 28730-1980 (Hunter Color Difference Notation Method), and is the chromaticness index calculated from the tristimulus values x, y, and z specified in JIS 8722 using the following formula: be.

aが0のとき無色、プラスになる程赤変、マイナスにな
る程緑変することを示す。
When a is 0, it is colorless; the more it becomes positive, the more it turns red, and the more it becomes negative, the more it turns green.

結果を第1表に示した。表中、TIP及び5t−Caは
次の化合物を示す。
The results are shown in Table 1. In the table, TIP and 5t-Ca represent the following compounds.

TNP:)リス(モノノニルフェニル及びジノニルフェ
ニル混合体)ホスファイト 5t−Caニステアリン酸カルシウム (以下余白) 発明の効果 第1表から判るように、リン系化合物であってもTIP
は効果が薄く、IrganoxloloやサノールLS
770を併用しないときは、ピンク変色はないが、試験
片は緑変化した。
TNP:) Lis (monononylphenyl and dinonylphenyl mixture) phosphite 5t-Ca calcium nistearate (hereinafter blank) Effects of the invention As can be seen from Table 1, even phosphorus compounds can be used as TIP.
is less effective, and Irganoxlolo and Sanol LS
When 770 was not used in combination, there was no pink discoloration, but the test piece turned green.

本発明組成物はいずれもピンク変色が著しく改善をみた
All of the compositions of the present invention showed marked improvement in pink discoloration.

Claims (1)

【特許請求の範囲】 ポリオレフィンに次の化合物を配合したことを特徴とす
る耐熱性及び耐候性にすぐれたポリオレフィン組成物。 (1)テトラキス〔メチレン−3−(3,5−ジ−te
rt−ブチル−4−ヒドロキシフェニル)プロピオネー
ト〕メタン (2)ビス(2,2′,6,6′−テトラアルキル−4
−ピペリジン)ジカルボキシレート (3)次の[1]〜[4]で示されるリン系安定剤の1
種又は2種以上。 [1]テトラキス−(2−tert−又は2,4−ジ−
tert−アルキルフェニル)−4,2′一又は4,4
′−ビアリ−レンジホスホナイト [2]水素添加ビスフェノール系−ペンタエリスリトー
ルホスファイトポリマー [3]ジC_1_0〜C_2_0アルキルペンタエリス
リトールジフォスファイト [4]ビス(2−tert又は2,4−ジ−tert−
アルキルフェニル)ペンタエリスリトールジホスファイ
[Scope of Claims] A polyolefin composition with excellent heat resistance and weather resistance, characterized by blending the following compound into a polyolefin. (1) Tetrakis [methylene-3-(3,5-di-te)
rt-butyl-4-hydroxyphenyl)propionate]methane(2)bis(2,2',6,6'-tetraalkyl-4
-piperidine) dicarboxylate (3) 1 of the phosphorus stabilizers shown in the following [1] to [4]
A species or two or more species. [1] Tetrakis-(2-tert- or 2,4-di-
tert-alkylphenyl)-4,2'-1 or 4,4
'-Biary diphosphonite [2] Hydrogenated bisphenol-pentaerythritol phosphite polymer [3] DiC_1_0-C_2_0 alkyl pentaerythritol diphosphite [4] Bis(2-tert or 2,4-di-tert-
alkylphenyl) pentaerythritol diphosphite
JP61160836A 1986-07-10 1986-07-10 Polyolefin composition Expired - Fee Related JPH0762094B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61160836A JPH0762094B2 (en) 1986-07-10 1986-07-10 Polyolefin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61160836A JPH0762094B2 (en) 1986-07-10 1986-07-10 Polyolefin composition

Publications (2)

Publication Number Publication Date
JPS6317944A true JPS6317944A (en) 1988-01-25
JPH0762094B2 JPH0762094B2 (en) 1995-07-05

Family

ID=15723462

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61160836A Expired - Fee Related JPH0762094B2 (en) 1986-07-10 1986-07-10 Polyolefin composition

Country Status (1)

Country Link
JP (1) JPH0762094B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02182961A (en) * 1988-12-29 1990-07-17 Toray Ind Inc Filament nonwoven fabric and production thereof
JPH02182960A (en) * 1988-12-29 1990-07-17 Toray Ind Inc Filament nonwoven fabric and production thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5425931A (en) * 1977-07-30 1979-02-27 Matsushita Electric Works Ltd Method of making inorganic hardened plate
JPS60120732A (en) * 1983-12-05 1985-06-28 Chisso Corp Stabilized polyolefin composition
JPS60124642A (en) * 1983-12-10 1985-07-03 Chisso Corp Stabilized polyolefin composition
JPS60130635A (en) * 1983-12-17 1985-07-12 Chisso Corp Stabilized polyolefin composition
JPS60199039A (en) * 1984-03-22 1985-10-08 Chisso Corp Stabilized polyolefin composition
JPS6153344A (en) * 1984-08-22 1986-03-17 Adeka Argus Chem Co Ltd Radiation-resistant polyolefin composition
JPS62138542A (en) * 1985-12-11 1987-06-22 Sumitomo Chem Co Ltd Polyolefin composition

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5425931A (en) * 1977-07-30 1979-02-27 Matsushita Electric Works Ltd Method of making inorganic hardened plate
JPS60120732A (en) * 1983-12-05 1985-06-28 Chisso Corp Stabilized polyolefin composition
JPS60124642A (en) * 1983-12-10 1985-07-03 Chisso Corp Stabilized polyolefin composition
JPS60130635A (en) * 1983-12-17 1985-07-12 Chisso Corp Stabilized polyolefin composition
JPS60199039A (en) * 1984-03-22 1985-10-08 Chisso Corp Stabilized polyolefin composition
JPS6153344A (en) * 1984-08-22 1986-03-17 Adeka Argus Chem Co Ltd Radiation-resistant polyolefin composition
JPS62138542A (en) * 1985-12-11 1987-06-22 Sumitomo Chem Co Ltd Polyolefin composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02182961A (en) * 1988-12-29 1990-07-17 Toray Ind Inc Filament nonwoven fabric and production thereof
JPH02182960A (en) * 1988-12-29 1990-07-17 Toray Ind Inc Filament nonwoven fabric and production thereof

Also Published As

Publication number Publication date
JPH0762094B2 (en) 1995-07-05

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