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JPS646661B2 - - Google Patents
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JPS646661B2 - - Google Patents

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Publication number
JPS646661B2
JPS646661B2 JP19774181A JP19774181A JPS646661B2 JP S646661 B2 JPS646661 B2 JP S646661B2 JP 19774181 A JP19774181 A JP 19774181A JP 19774181 A JP19774181 A JP 19774181A JP S646661 B2 JPS646661 B2 JP S646661B2
Authority
JP
Japan
Prior art keywords
vinyl chloride
chloride resin
parts
present
meth
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP19774181A
Other languages
Japanese (ja)
Other versions
JPS58101138A (en
Inventor
Mitsuhiro Isomichi
Futoshi Takimoto
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.)
DIC Corp
Original Assignee
Dainippon Ink and Chemicals Co 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 Dainippon Ink and Chemicals Co Ltd filed Critical Dainippon Ink and Chemicals Co Ltd
Priority to JP19774181A priority Critical patent/JPS58101138A/en
Publication of JPS58101138A publication Critical patent/JPS58101138A/en
Publication of JPS646661B2 publication Critical patent/JPS646661B2/ja
Granted legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 本発明は屋外暴露に対して安定な塩化ビニル樹
脂組成物に関するものである。 塩化ビニル樹脂の着色成形品を日光の直射下で
使用すると、日光暴露部の表面が粉をふいた如く
白つぽく着色して成形品本来の色調が大巾に変化
する結果、成形品の外観が著るしく損なわれるこ
とは周知の通りである。この白つぽく着色する現
象は屋外暴露で発生するが、合成樹脂成形品の耐
候性促進試験機として汎用されているウエザオメ
ーターでは再現し得ない特異な現象で、チヨーキ
ングと呼ばれている。 ところで雨樋、デツキ材等は屋外で特に長期間
使用されるため、かかる用途に塩化ビニル樹脂成
形品を利用する場合、チヨーキング現象の発生を
抑制して発生時期を遅延させる目的で、従来より
種々の安定剤、紫外線吸収剤、光劣化防止剤等を
塩化ビニル樹脂に添加することが行われている。
なかでも有機錫化合物、カドミウムの金属石鹸、
鉛の金属石鹸等は耐候性を向上させチヨーキング
抑制効果が優れているため汎用されているが、こ
れらの安定剤を含む塩化ビニル樹脂であつても2
〜10ケ月後にはチヨーキング現象が発生し始め
る。このように従来チヨーキング抑制効果の秀で
ている安定剤を添加した塩化ビニル樹脂であつて
も、長期間屋外暴露する用途には到底充分なもの
とは言えなかつた。 本発明者等は、かかる状況に鑑み鋭意研究の結
果、(メタ)アクリル酸の銅塩および/又は(メ
タ)アクリル酸のコバルト塩が卓越したチヨーキ
ング抑制効果を有し、しかもその効果を長時間持
続することを見い出し、本発明を完成するに至つ
た。 すなわち、本発明は、(メタ)アクリル酸の銅
塩および/又は(メタ)アクリル酸のコバルト塩
を含有する塩化ビニル樹脂組成物を提供するもの
である。 本発明で用いる塩化ビニル樹脂とは、塩化ビニ
ル単独重合体および塩化ビニルを主成分とする共
重合体を言い、通常成形用に使用されている塩化
ビニル系樹脂のすべてを含む。 本発明で塩化ビニル樹脂に混合して用いられる
(メタ)アクリル酸の銅塩および/又は(メタ)
アクリル酸のコバルト塩の使用割合は、塩化ビニ
ル樹脂100重量部(以下、単に部と記す。)に対し
て、通常0.01〜10部、好ましくは0.1〜2部の範
囲である。 また本発明の塩化ビニル樹脂組成物には、従来
から塩化ビニル樹脂に使用されているチヨーキン
グ防止剤、例えば酸化マグネシウム、水酸化マグ
ネシウム、2―ヒドロキシ―4―オクトキシベン
ゾフエノン、2―(2′―ヒドロキシ―5―メチル
フエニル)ベンゾトリアゾール、4―ベンゾイル
オキシ―2,2,6,6―テトラメチルピペリジ
ン、ジブチルジチオカルバミン酸ニツケル等を併
用することもできる。更に可塑剤、安定剤、滑
剤、着色剤等の周知の添加剤が併存していても差
し支えはなく、特に鉛系安定剤が併存している場
合、チヨーキング防止効果は顕著である。 塩化ビニル樹脂との混合方法は、従来周知のチ
ヨーキング防止剤と塩化ビニル樹脂の混合方法と
同様に、微粉末状で使用し、また充分に混練をす
ることが好ましく、例えば、塩化ビニル樹脂に直
接添加して混合する方法、可塑剤、安定剤、滑
剤、着色剤等の他の周知の添加剤にあらかじめ含
有させておき、それを塩化ビニル樹脂に添加して
混合する方法があるが、それらを均一に分散させ
易いという点で、後者の方法が好ましい。 かくして得られる本発明の組成物は、屋外暴露
に対して安定であるため、屋外で使用する機器、
用具に利用してもチヨーキングの発生が長期間抑
制されるので、雨樋、デツキ材等の用途に最適で
ある。次に本発明を実施例により説明する。 実施例 1 塩化ビニル樹脂〔住友化学(株)製スミリツトSX
―11F〕100部に 三塩基性硫酸鉛 0.8部 二塩基性ステアリン酸鉛 0.4部 ステアリン酸鉛 1.3部 ステアリン酸カルシウム 0.4部 ポリエチレンワツクス 0.3部 を添加混合して調整したコンパウンド103.2部に
弁柄〔戸田工業(株)製100R〕0.7部およびアクリル
酸銅1.0部を添加混合し、155℃6インチの加熱二
本ロールで5分間練肉後、180℃の加熱プレスで
1mm厚のシートを作成し、このシートを屋外暴露
試験に供し、チヨーキング現象の発生を調べた。 実施例2〜3および比較例1 アクリル酸銅1.0部の代わりに表1に示す化合
物を表1に示す使用量で用いた以外は実施例1と
同様にしてシートを作成し、屋外暴露試験に供し
た。 以上の各例における暴露12ケ月後、18ケ月後、
24ケ月後の試料表面の色差を表1に示す。 【表】
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to vinyl chloride resin compositions that are stable against outdoor exposure. If a colored molded product made of vinyl chloride resin is used under direct sunlight, the surface of the exposed part will become white, as if it has been wiped with powder, and the original color tone of the molded product will change drastically, resulting in a change in the appearance of the molded product. It is well known that this can be severely impaired. This phenomenon of whitish coloration occurs when exposed outdoors, but it is a unique phenomenon that cannot be reproduced with a weatherometer, which is commonly used as a weather resistance acceleration tester for synthetic resin molded products, and is called yoking. By the way, rain gutters, decking materials, etc. are used outdoors for long periods of time, so when using vinyl chloride resin molded products for such purposes, various conventional methods have been used to suppress the occurrence of the choke phenomenon and delay its occurrence. Stabilizers, ultraviolet absorbers, photodegradation inhibitors, etc. are added to vinyl chloride resin.
Among them, organotin compounds, cadmium metal soaps,
Lead metal soaps are commonly used because they improve weather resistance and are effective in suppressing tyoke, but even vinyl chloride resins containing these stabilizers have 2
After ~10 months, the yoking phenomenon begins to occur. As described above, even vinyl chloride resins to which stabilizers have been added which have an excellent effect of suppressing yoking cannot be said to be sufficient for long-term outdoor exposure applications. In view of this situation, the present inventors have conducted extensive research and have found that copper salts of (meth)acrylic acid and/or cobalt salts of (meth)acrylic acid have an outstanding choke-suppressing effect, and that the effect can be maintained for a long time. The inventors have found that the present invention lasts, and have completed the present invention. That is, the present invention provides a vinyl chloride resin composition containing a copper salt of (meth)acrylic acid and/or a cobalt salt of (meth)acrylic acid. The vinyl chloride resin used in the present invention refers to vinyl chloride homopolymers and copolymers containing vinyl chloride as a main component, and includes all vinyl chloride resins commonly used for molding. Copper salt of (meth)acrylic acid and/or (meth) used by mixing with vinyl chloride resin in the present invention
The proportion of the cobalt salt of acrylic acid used is usually 0.01 to 10 parts, preferably 0.1 to 2 parts, per 100 parts by weight of the vinyl chloride resin (hereinafter simply referred to as parts). In addition, the vinyl chloride resin composition of the present invention may contain anti-choking agents conventionally used in vinyl chloride resins, such as magnesium oxide, magnesium hydroxide, 2-hydroxy-4-octoxybenzophenone, 2-(2 '-Hydroxy-5-methylphenyl)benzotriazole, 4-benzoyloxy-2,2,6,6-tetramethylpiperidine, nickel dibutyldithiocarbamate, etc. can also be used in combination. Furthermore, there is no problem even if well-known additives such as plasticizers, stabilizers, lubricants, colorants, etc. are co-present, and especially when a lead-based stabilizer is co-present, the anti-choke effect is remarkable. The mixing method with the vinyl chloride resin is similar to the conventional mixing method of the anti-choking agent and the vinyl chloride resin, and it is preferable to use it in fine powder form and thoroughly knead it. There is a method of adding and mixing, and a method of pre-containing other well-known additives such as plasticizers, stabilizers, lubricants, colorants, etc., and adding them to vinyl chloride resin and mixing. The latter method is preferred in that it is easier to disperse uniformly. The composition of the present invention obtained in this way is stable against outdoor exposure, so it can be used in equipment used outdoors,
Even when used in tools, the occurrence of yoking is suppressed for a long period of time, making it ideal for uses such as rain gutters and decking materials. Next, the present invention will be explained by examples. Example 1 Vinyl chloride resin [Sumirit SX manufactured by Sumitomo Chemical Co., Ltd.
-11F] Add and mix 100 parts of tribasic lead sulfate 0.8 parts dibasic lead stearate 0.4 parts Lead stearate 1.3 parts Calcium stearate 0.4 parts Polyethylene wax 0.3 parts to 103.2 parts of a compound prepared by mixing Bengara [Toda] 0.7 parts of 100R produced by Kogyo Co., Ltd. and 1.0 parts of copper acrylate were added and mixed, kneaded for 5 minutes with two 6-inch rolls heated at 155°C, and made into a 1 mm thick sheet using a heated press at 180°C. This sheet was subjected to an outdoor exposure test to examine the occurrence of the yoking phenomenon. Examples 2 to 3 and Comparative Example 1 Sheets were prepared in the same manner as in Example 1, except that the compounds shown in Table 1 were used in the amounts shown in Table 1 instead of 1.0 part of copper acrylate, and the sheets were subjected to an outdoor exposure test. provided. After 12 months and 18 months of exposure in each of the above cases,
Table 1 shows the color difference on the sample surface after 24 months. 【table】

Claims (1)

【特許請求の範囲】[Claims] 1 (メタ)アクリル酸の銅塩および/又は(メ
タ)アクリル酸のコバルト塩を含有する塩化ビニ
ル樹脂組成物。
1. A vinyl chloride resin composition containing a copper salt of (meth)acrylic acid and/or a cobalt salt of (meth)acrylic acid.
JP19774181A 1981-12-10 1981-12-10 Vinyl chloride resin composition Granted JPS58101138A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19774181A JPS58101138A (en) 1981-12-10 1981-12-10 Vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19774181A JPS58101138A (en) 1981-12-10 1981-12-10 Vinyl chloride resin composition

Publications (2)

Publication Number Publication Date
JPS58101138A JPS58101138A (en) 1983-06-16
JPS646661B2 true JPS646661B2 (en) 1989-02-06

Family

ID=16379564

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19774181A Granted JPS58101138A (en) 1981-12-10 1981-12-10 Vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPS58101138A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1085987A (en) * 1976-01-12 1980-09-16 Arthur W. Mcrowe Vinyl chloride polymers containing copper oxalate

Also Published As

Publication number Publication date
JPS58101138A (en) 1983-06-16

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