JPH0733936A - Chlorine-containing resin composition - Google Patents

Chlorine-containing resin composition

Info

Publication number
JPH0733936A
JPH0733936A JP22495193A JP22495193A JPH0733936A JP H0733936 A JPH0733936 A JP H0733936A JP 22495193 A JP22495193 A JP 22495193A JP 22495193 A JP22495193 A JP 22495193A JP H0733936 A JPH0733936 A JP H0733936A
Authority
JP
Japan
Prior art keywords
mercaptide
chlorine
octyltin
alkyltin
sulfide
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.)
Pending
Application number
JP22495193A
Other languages
Japanese (ja)
Inventor
Koichi Ogata
康一 小形
Hideo Tsujimoto
英雄 辻本
Minori Nakashita
未徳 中下
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.)
Sakai Chemical Industry Co Ltd
Original Assignee
Sakai Chemical Industry 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 Sakai Chemical Industry Co Ltd filed Critical Sakai Chemical Industry Co Ltd
Priority to JP22495193A priority Critical patent/JPH0733936A/en
Publication of JPH0733936A publication Critical patent/JPH0733936A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE:To improve the resistance to initial coloration, thermal stability, etc., of the title compsn. by compounding a chlorine-contg. resin with methyltin mercaptide, octyltin mercaptide, and an alkyltin sulfide. CONSTITUTION:The compsn. excellent in resistance to initial coloration, heat resistance, etc., is obtd. by compounding a chlorine-contg. resin (e.g. a vinyl chloride-vinyl acetate copolymer) with methyltin mercaptide, octyltin mercaptide, and an alkyltin sulfide in an amt. of 0.01-5 pts.wt., pref. 0.1-3 pts.wt., based on 100 pts.wt. the resin. Methyl- or octyltin mercaptide is produced by reacting methyl-or octyltin chloride or oxide with a compd. represented by HS (CH2)nCOOR (wherein R is 1-23C alkyl or alkenyl; and n is 1-2). An alkyltin sulfide is produced by reacting an alkyltin chloride with sodium sulfide.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は新規な塩素含有樹脂組成
物に関する。
TECHNICAL FIELD The present invention relates to a novel chlorine-containing resin composition.

【0002】[0002]

【従来の技術】ポリ塩化ビニル等の塩素含有樹脂組成物
は、透明性、強度、加工性、着色性等に優れ、しかも安
価であるため、フィルム、シート、パイプ、継手、さら
に近年は、車輌用レザー等にも多量に使用されている。
2. Description of the Related Art Chlorine-containing resin compositions such as polyvinyl chloride are excellent in transparency, strength, processability, colorability, etc., and are inexpensive, so that they can be used in films, sheets, pipes, joints, and more recently in vehicles. It is also used in large quantities for leather and other products.

【0003】塩素含有樹脂は、光や熱にさらされると、
主として脱塩化水素反応に起因する分解劣化を起こし、
共役二重結合、いわゆるポリエン構造を生じて着色す
る。また、さらに分解が進むと、分子切断や架橋結合が
発生し、機械的強度等が低下して脆くなる。
When chlorine-containing resin is exposed to light or heat,
Decomposition and deterioration mainly caused by dehydrochlorination reaction,
It produces a conjugated double bond, a so-called polyene structure, which causes coloration. Further, if the decomposition further proceeds, molecular cutting or cross-linking occurs, resulting in a decrease in mechanical strength and the like, resulting in brittleness.

【0004】そこで、成形加工時の熱によって上記脱塩
化水素反応が発生して、製品の色調が悪化したり、製品
の物性が低下したりすることを防止するために、塩素含
有樹脂組成物には、各種の安定剤が配合されている。
Therefore, in order to prevent the dehydrochlorination reaction from occurring due to the heat during molding, resulting in deterioration of the color tone of the product and deterioration of the physical properties of the product, a chlorine-containing resin composition is added. Is mixed with various stabilizers.

【0005】安定剤としては、鉛、カドミウム、亜鉛、
カルシウム等の有機酸塩類及び有機錫化合物が最も多く
使用されている。
Stabilizers include lead, cadmium, zinc,
Organic acid salts such as calcium and organic tin compounds are most often used.

【0006】更に最近は無毒性の樹脂製品に対する要望
が高まり、使用する安定剤として亜鉛、カルシウムの有
機酸塩類、メチル錫化合物、オクチル錫化合物の需要が
増加している。
Further, recently, the demand for non-toxic resin products has increased, and the demand for zinc, calcium organic acid salts, methyltin compounds, and octyltin compounds as stabilizers has been increasing.

【0007】[0007]

【発明が解決しようとする課題】本発明は特に無毒性の
安定剤に注目し、現状を概観すると、既存の亜鉛、カル
シウム有機酸塩類、メチル錫化合物、オクチル錫化合物
はそれなりに性能を有し使用されているがなお初期着色
性、耐勢性、製品の外観等で問題がある。
The present invention pays particular attention to non-toxic stabilizers, and in view of the present situation, existing zinc, calcium organic acid salts, methyltin compounds and octyltin compounds have their own performance. Although it is used, it still has problems in initial colorability, durability, and product appearance.

【0008】[0008]

【問題を解決するための手段】本発明者らはかかる現状
に艦み、鋭意検討の結果、メチル錫メルカプチド、オク
チル錫メルカプチド及びアルキル錫サルファイドを含有
する塩素含有樹脂組成物により上記問題を改善し得るこ
とを見出し本発明を完成した。
[Means for Solving the Problems] The present inventors have made strenuous efforts to solve the above problems, and as a result of intensive studies, the above problems were solved by a chlorine-containing resin composition containing methyltin mercaptide, octyltin mercaptide and alkyltin sulfide. The present invention has been completed by finding that it can be obtained.

【0009】メチル錫メルカプチド、オクチル錫メルカ
プチドはそれぞれモノメチル錫メルカプチド、ジメチル
錫メルカプチドのいずれか単独あるいは混合物、モノオ
クチル錫メルカプチド、ジオクチル錫メルカプチドのい
ずれか単独あるいは混合物で良い。
The methyltin mercaptide and octyltin mercaptide may be any one of monomethyltin mercaptide and dimethyltin mercaptide alone or a mixture thereof, and any one of monooctyltin mercaptide and dioctyltin mercaptide alone or a mixture thereof.

【0010】上記錫化合物はメチルあるいはオクチル錫
クロライドあるいはオキサイドとHS(CHCO
ORあるいはHS(CHOCORで表わされる化
合物を反応させてアルキル錫メルカプチドを製造する。
The tin compound is methyl or octyl tin chloride or oxide and HS (CH 2 ) n CO 2.
An alkyl tin mercaptide is produced by reacting a compound represented by OR or HS (CH 2 ) n OCOR.

【0011】上記でRはCが1〜23のアルキル又はア
ルケニル基、nは1あるいは2である。
In the above, R is an alkyl or alkenyl group in which C is 1 to 23, and n is 1 or 2.

【0012】又該化合物はHSRCOOHとROHのエ
ステルあるいはHSROHとRCOOHのエステルであ
る。
The compound is also an ester of HSRCOOH and ROH or an ester of HSROH and RCOOH.

【0013】 る化合物群であり、通常以下の方法で製造される。[0013] It is a group of compounds that are usually produced by the following method.

【0014】モノ又は及びジアルキル錫クロライドを硫
化ソーダ、水硫化ソーダ又は硫化水素と反応させること
により製造される。
It is prepared by reacting mono- and / or dialkyl tin chloride with sodium sulfide, sodium hydrosulfide or hydrogen sulfide.

【0015】場合によってはモノ又はジメチル(オクチ
ル)錫メルカプチドを合成後その中へ上記原料を投入し
て反応させても良い。
In some cases, mono- or dimethyl (octyl) tin mercaptide may be synthesized and then the above-mentioned raw materials may be added thereto for reaction.

【0016】アルキル錫サルファイドのアルキル基はメ
チル、ブチル、オクチルいずれでも良い。
The alkyl group of the alkyltin sulfide may be any of methyl, butyl and octyl.

【0017】メチル錫メルカプチド、オクチル錫メルカ
プチド及びアルキル錫サルファイドの塩素含有樹脂に含
有させる量は樹脂100重量部に対し、0.01重量部
〜5重量部以下であり、好ましくは0.1重量部〜3重
量部である。
The amount of methyltin mercaptide, octyltin mercaptide and alkyltin sulfide contained in the chlorine-containing resin is 0.01 to 5 parts by weight, preferably 0.1 parts by weight, based on 100 parts by weight of the resin. ~ 3 parts by weight.

【0018】また本発明において、従来より塩素含有樹
脂に使用されているその他の安定剤、難燃剤、充填剤、
熱安定化助剤、酸化防止剤、紫外線吸収剤、エポキシ化
合物、滑剤、顔料等を併用して良いのは言うまでもな
い。
Further, in the present invention, other stabilizers, flame retardants, fillers, which are conventionally used for chlorine-containing resins,
It goes without saying that a heat stabilization aid, an antioxidant, an ultraviolet absorber, an epoxy compound, a lubricant, a pigment and the like may be used in combination.

【0019】本発明の塩素含有樹脂とは、塩化ビニル単
独重合体または塩化ビニルを主体とした樹脂であって例
えば、塩化ビニルと酢酸ビニル、塩化ビニリデン、エチ
レン、プロピレン、メタアクリル酸エステル、ウレタン
樹脂との共重合体やグラフト重合体あるいはこれら樹脂
とのブレンド物等である。
The chlorine-containing resin of the present invention is a vinyl chloride homopolymer or a resin mainly composed of vinyl chloride, and examples thereof include vinyl chloride and vinyl acetate, vinylidene chloride, ethylene, propylene, methacrylic acid ester and urethane resin. And a copolymer with these resins or a blend with these resins.

【0020】[0020]

【実施例】以下本発明を実施例に基づいて具体的に説明
する。
EXAMPLES The present invention will be specifically described below based on examples.

【0021】実施例 表1に記載した各成分を含有するサンプルを用いブラベ
ンダー社製プラストグラフでニーダー温度180℃、ロ
ーター回転数40rpm、サンプル仕込量70gの条件
でテストした。
Example A sample containing each component shown in Table 1 was tested by a Brabender Plastograph under the conditions of a kneader temperature of 180 ° C., a rotor rotation number of 40 rpm, and a sample preparation amount of 70 g.

【0022】結果は表1に示す。The results are shown in Table 1.

【表1】 [Table 1]

【0023】表2に記載した各成分を含有するサンプル
を90℃で20lスーパーミキサーでコンパウンディン
グし下記条件でパイプを押出成形した。
Samples containing the components shown in Table 2 were compounded with a 20 l supermixer at 90 ° C. and a pipe was extruded under the following conditions.

【0024】押出条件 押 出 機:50mmφ単軸押出機 スクリユー:L/D=22,CR=3,回転数20rp
m ダ イ:20mmφ、パイプ用ダイ サイジング:バキュームサイジング 設定温度:C150℃,C160℃,C170
℃,H180℃,D200℃,D200℃ 成形は全て粉体押出により成形。結果は表3に示す。
Extrusion conditions Extruder: 50 mmφ single screw extruder Screen: L / D = 22, CR = 3, rotation speed 20 rp
m Dye: 20 mmφ, pipe die sizing: vacuum sizing Setting temperature: C 1 150 ° C, C 2 160 ° C, C 3 170
℃, H 1 180 ℃, D 1 200 ℃, D 2 200 ℃ All molding is by powder extrusion. The results are shown in Table 3.

【0025】[0025]

【表2】 [Table 2]

【0026】[0026]

【表3】 [Table 3]

【0027】[0027]

【発明の効果】上記から分る如く、本発明に係る塩素含
有樹脂組成物は従来に見られない優れた勢安定性、初期
着色性を示す。
As can be seen from the above, the chlorine-containing resin composition according to the present invention exhibits excellent stability and initial colorability that have not been found in the past.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】メチル錫メルカプチド、オクチル錫メルカ
プチド及びアルキル錫サルファイドを含有する塩素含有
樹脂組成物。
1. A chlorine-containing resin composition containing methyltin mercaptide, octyltin mercaptide and alkyltin sulfide.
JP22495193A 1993-07-21 1993-07-21 Chlorine-containing resin composition Pending JPH0733936A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22495193A JPH0733936A (en) 1993-07-21 1993-07-21 Chlorine-containing resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22495193A JPH0733936A (en) 1993-07-21 1993-07-21 Chlorine-containing resin composition

Publications (1)

Publication Number Publication Date
JPH0733936A true JPH0733936A (en) 1995-02-03

Family

ID=16821753

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22495193A Pending JPH0733936A (en) 1993-07-21 1993-07-21 Chlorine-containing resin composition

Country Status (1)

Country Link
JP (1) JPH0733936A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8266769B2 (en) 2007-10-12 2012-09-18 Maisy And Mary, Llc Clip for ornamentation and method of using same
JP2016069598A (en) * 2014-10-01 2016-05-09 ダイヤプラスフィルム株式会社 Polyvinyl chloride resin film and laminate sheet

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8266769B2 (en) 2007-10-12 2012-09-18 Maisy And Mary, Llc Clip for ornamentation and method of using same
JP2016069598A (en) * 2014-10-01 2016-05-09 ダイヤプラスフィルム株式会社 Polyvinyl chloride resin film and laminate sheet

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