JPH0967491A - Vinyl chloride resin composition - Google Patents

Vinyl chloride resin composition

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Publication number
JPH0967491A
JPH0967491A JP22637495A JP22637495A JPH0967491A JP H0967491 A JPH0967491 A JP H0967491A JP 22637495 A JP22637495 A JP 22637495A JP 22637495 A JP22637495 A JP 22637495A JP H0967491 A JPH0967491 A JP H0967491A
Authority
JP
Japan
Prior art keywords
vinyl chloride
chloride resin
resin composition
parts
hydrotalcite
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
JP22637495A
Other languages
Japanese (ja)
Inventor
Koushiki Aoyanagi
▲こう▼識 青柳
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 JP22637495A priority Critical patent/JPH0967491A/en
Publication of JPH0967491A publication Critical patent/JPH0967491A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PROBLEM TO BE SOLVED: To obtain the subject composition excellent in thermal stability in its molding processing and in chalking resistance of the molded products thereof. SOLUTION: This resin composition comprises 100 pts.wt. of a vinyl chloride resin, a total of 0.005-1 pt.wt. of a copper o,o'-dialkyl-dithiophosphate and/or stannous acetate, and 0.1-3 pts.wt. of hydrotalcite, and pref., a coloring ingredient. When compared to conventional such compositions, this resin composition is excellent in thermal stability during its long-term molding processing under heating and weatherability of the molded products thereof, in particular, can suppress chalking of the molded products thereof such as gutters or deck materials over a long period.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は耐候性、特に耐チョ
ーキング性に優れる塩化ビニル樹脂組成物、特に着色さ
れた塩化ビニル樹脂組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a vinyl chloride resin composition excellent in weather resistance, particularly choking resistance, and more particularly to a colored vinyl chloride resin composition.

【0002】[0002]

【従来の技術】塩化ビニル樹脂は、顔料等で着色され
て、パイプ、雨樋、デッキ材、窓枠等の成形品となって
屋外で利用される場合が多い。
2. Description of the Related Art Vinyl chloride resin is often used outdoors as a molded product such as a pipe, a rain gutter, a deck material, a window frame or the like, which is colored with a pigment or the like.

【0003】しかし着色した成形物を屋外に暴露する
と、色の変退色ばかりでなく日光に暴露された部分の表
面が粉を吹いたように白く変色する、いわゆるチョーキ
ング現象(白化現象)を起こすので、著しく外観が損な
われるとともに機械的強度も低下するという問題があっ
た。
However, when a colored molded article is exposed to the outside, not only the discoloration and fading of the color but also the so-called chalking phenomenon (whitening phenomenon) occurs, in which the surface of the portion exposed to the sunlight discolors white as if it were blowing powder. However, there is a problem that the appearance is significantly impaired and the mechanical strength is also reduced.

【0004】従来、このような欠点を改善するため、必
要に応じて金属石鹸、鉛系化合物、有機錫系化合物等の
熱安定剤の他、紫外線吸収剤、酸化防止剤、可塑剤、滑
剤、充填剤、着色剤を選択添加するとともに、ナフテン
酸金属塩、ニッケルキレート錯化合物、チオシアン酸金
属塩などのチョーキング防止剤を添加した塩化ビニル樹
脂の成形品が作られている。
Conventionally, in order to improve such drawbacks, heat stabilizers such as metal soaps, lead compounds and organotin compounds, as well as ultraviolet absorbers, antioxidants, plasticizers, lubricants, and Molded articles of vinyl chloride resin have been made by selectively adding a filler and a colorant, and adding a choking inhibitor such as a metal salt of naphthenic acid, a nickel chelate complex compound, and a metal salt of thiocyanate.

【0005】また特開平1−131267号公報或いは
特開平5−287148号公報等に示されるo,o’−
ジアルキルジチオリン酸銅或いはジアルキルジチオカル
バミン酸金属塩を添加することによって、従来のものよ
り長期間にわたってチョーキングを抑制することも行わ
れてきた。
Further, o, o'-shown in JP-A-1-131267 or JP-A-5-287148.
The addition of copper dialkyldithiophosphate or metal salt of dialkyldithiocarbamate has also been carried out to suppress chalking for a longer period of time than conventional ones.

【0006】[0006]

【発明が解決しようとする課題】しかし、チョーキング
を抑制しようとすると、塩化ビニル樹脂の熱安定性が低
下するため、成形時の熱分解はある程度避けられない。
従って成形品ではチョーキング防止剤の本来の効果を発
揮し得ないという問題があって、未だ充分満足すべき製
品が提供されるに至っていない。
However, if an attempt is made to suppress choking, the thermal stability of the vinyl chloride resin will decrease, and thermal decomposition during molding cannot be avoided to some extent.
Therefore, there is a problem that the original effect of the anti-choking agent cannot be exhibited in a molded product, and a product which is sufficiently satisfactory has not yet been provided.

【0007】[0007]

【課題を解決するための手段】本発明者は上記の問題点
を解決すべく鋭意研究を進めた結果、塩化ビニル樹脂に
特定組成比でo,o’−ジアルキルジチオリン酸銅及び
/又は酢酸第一錫及びハイドロタルサイトを添加するこ
とにより、従来のものと比較し、熱安定性がよく、長期
間にわたって成形品のチョーキングを抑制できる塩化ビ
ニル樹脂組成物を得ることを見出し、本発明を完成する
に至った。
As a result of intensive studies to solve the above problems, the present inventor has found that o, o'-dialkyldithiophosphoric acid copper and / or acetic acid diacetate can be added to vinyl chloride resin at a specific composition ratio. It was found that the addition of istin and hydrotalcite provides a vinyl chloride resin composition having better thermal stability than conventional ones and capable of suppressing the chalking of molded articles over a long period of time, and completed the present invention. Came to do.

【0008】即ち本発明は、塩化ビニル樹脂100重量
部に対して、o,o’−ジアルキルジチオリン酸銅及び
/又は酢酸第一錫の夫々の単独又は合計量で0.005
〜1重量部、及びハイドロタルサイトを0.1〜3重量
部含有させることにより、成形時の熱安定性に優れ、し
かも成形品の白化現象が著しく抑制された塩化ビニル樹
脂組成物を提供するものである。
That is, according to the present invention, the amount of each of o, o'-dialkyldithiophosphate copper and / or stannous acetate, alone or in total, is 0.005 with respect to 100 parts by weight of vinyl chloride resin.
By containing 1 to 1 part by weight and 0.1 to 3 parts by weight of hydrotalcite, a vinyl chloride resin composition having excellent thermal stability at the time of molding and significantly suppressing the whitening phenomenon of the molded article is provided. It is a thing.

【0009】本発明で用いるo,o’−ジアルキルジチ
オリン酸銅としては、例えばアルキル基として炭素数3
〜10の直鎖又は分枝鎖アルキル基を有するものが挙げ
られるが、なかでもo,o’−ジn−ブチルジチオリン
酸銅及びo,o’−ジ(2−エチルヘキシル)ジチオリ
ン酸銅が好ましい。
The o, o'-dialkyldithiophosphate copper used in the present invention has, for example, 3 carbon atoms as an alkyl group.
Examples thereof include those having 10 to 10 linear or branched alkyl groups, and among them, o, o'-di-n-butyldithiophosphate copper and o, o'-di (2-ethylhexyl) dithiophosphate copper are preferred. .

【0010】本発明で使用されるハイドロタルサイトは
Mg6Al2(OH)16CO3・4H2O 又は3MgO・
ZnOAl23CO3・H2Oで示されるものであり、い
ずれもが同様に使用できる。
The hydrotalcite used in the present invention is Mg 6 Al 2 (OH) 16 CO 3 .4H 2 O or 3MgO.
ZnOAl 2 O 3 CO 3 · H are those represented by 2 O, both can be used as well.

【0011】本発明の対象とする塩化ビニル樹脂は、塩
化ビニルの単独或いは共重合体及び塩素化塩化ビニル樹
脂である。これらの樹脂には、通常使用に際して添加さ
れる金属石鹸、鉛化合物、有機錫系化合物、紫外線吸収
剤、紫外線安定剤、滑剤、充填剤、補強剤、可塑剤、着
色剤等が混合されていても支障がないことは言うまでも
ない。
The vinyl chloride resin which is the object of the present invention is a homo- or copolymer of vinyl chloride and a chlorinated vinyl chloride resin. These resins are mixed with metal soaps, lead compounds, organotin compounds, UV absorbers, UV stabilizers, lubricants, fillers, reinforcing agents, plasticizers, colorants, etc., which are usually added during use. Needless to say, there is no problem.

【0012】本発明において使用されるo,o’−ジア
ルキルジチオリン酸銅及び/又は酢酸第一錫の量は単独
又は合計で、塩化ビニル樹脂100部に対し0.005
〜1重量部好ましくは0.05〜0.5重量部である
が、塩化ビニル樹脂が明るい色に着色される場合には、
酢酸第一錫の割合を小さくすることにより、明るい色を
長期間にわたって保持することができる。
The amount of copper o, o'-dialkyldithiophosphate and / or stannous acetate used in the present invention, alone or in total, is 0.005 per 100 parts of vinyl chloride resin.
1 to 1 part by weight, preferably 0.05 to 0.5 part by weight, but when the vinyl chloride resin is colored in a bright color,
By reducing the proportion of stannous acetate, bright colors can be retained for a long period of time.

【0013】ハイドロタルサイトの使用量は塩化ビニル
樹脂100部に対して0.1〜3重量部好ましくは0.
1〜2重量部の範囲である。これらを塩化ビニル樹脂中
に混合する方法としては、o,o’−ジアルキルジチオ
リン酸及び/又は酢酸第一錫及びハイドロタルサイトを
それぞれ塩化ビニル樹脂に直接添加混合してもよいし、
顔料などの他の添加物と共に予め混合したものを樹脂に
添加混合してもよい。
The amount of hydrotalcite used is 0.1 to 3 parts by weight, preferably 0.
It is in the range of 1 to 2 parts by weight. As a method of mixing these into a vinyl chloride resin, o, o'-dialkyldithiophosphoric acid and / or stannous acetate and hydrotalcite may be directly added to and mixed with the vinyl chloride resin,
What was mixed beforehand with other additives, such as a pigment, may be added and mixed with the resin.

【0014】[0014]

【発明の実施の形態】本発明は以上の如きものであるか
ら、その実施に当たっては、塩化ビニル樹脂100重量
部に対して、o,o’−ジアルキルジチオリン酸銅及び
酢酸第一錫の内のどちらか一方、または両方を併せて
0.005〜1重量部好ましくは0.05〜0.5重量
部と、更にハイドロタルサイトを0.1〜3重量部好ま
しくは0.1〜2重量部添加し、必要に応じて所望の色
に着色するための着色成分及びその他の各種添加剤を加
えて加熱混練し、例えば成形用の樹脂組成物とする。
BEST MODE FOR CARRYING OUT THE INVENTION The present invention is as described above. Therefore, in carrying out the present invention, in 100 parts by weight of a vinyl chloride resin, one of o, o'-dialkyldithiophosphate copper and stannous acetate is used. Either one or both, 0.005 to 1 part by weight, preferably 0.05 to 0.5 part by weight, and 0.1 to 3 parts by weight of hydrotalcite, preferably 0.1 to 2 parts by weight. The resin composition is added, and if necessary, a coloring component for coloring to a desired color and other various additives are added and kneaded by heating to obtain a resin composition for molding, for example.

【0015】また、塩化ビニル樹脂又はその他の適当な
担体樹脂に対し、塩化ビニル樹脂以外の本発明の他の成
分を高配合比で添加して、いわゆるマスターバッチを予
め製造し、これを大比率の塩化ビニル樹脂と加熱混練し
て目的の樹脂組成物とすることもできる。
A so-called masterbatch is prepared in advance by adding the other components of the present invention other than the vinyl chloride resin to the vinyl chloride resin or other suitable carrier resin in a high mixing ratio, and a large proportion of this is prepared. It is also possible to heat and knead with the vinyl chloride resin to produce the desired resin composition.

【0016】[0016]

【実施例】以下に実施例及び比較例を示して本発明をさ
らに具体的に説明する。なお、例中の部はすべて重量部
である。
EXAMPLES The present invention will be described more specifically by showing Examples and Comparative Examples below. All parts in the examples are parts by weight.

【0017】実施例1〜10 塩化ビニル樹脂100部、(重合度1100)ステアリ
ン酸カルシウム0.5部、ステアリン酸亜鉛0.5部、
ジブチルチンジマレート0.1部、弁柄1部にo,o’
−ジアルキルジチオリン酸銅及びハイドロタルサイトを
表1に記載の部数で配合した。これを均一に分散混合し
た後、180℃の2本ロールで3分間混練し、厚さ1.
5mmのシートを得た。
Examples 1 to 10 Vinyl chloride resin 100 parts, (degree of polymerization 1100) calcium stearate 0.5 parts, zinc stearate 0.5 parts,
0.1 parts of dibutyltin dimalate, o, o 'for 1 part of rouge
-Copper dialkyldithiophosphate and hydrotalcite were blended in the numbers shown in Table 1. This was uniformly dispersed and mixed, and then kneaded with two rolls at 180 ° C. for 3 minutes to give a thickness of 1.
A 5 mm sheet was obtained.

【0018】このシートを190℃のオーブン中に入
れ、熱安定性試験を行い、黒変するまでの時間を測定し
た。また同様に作成したシートを185℃の熱プレスで
1mm厚のシートに作成し屋外暴露した。暴露12ヶ月、
24ヶ月、30ヶ月後のテストピースを測色してチョー
キング度合いを△Yで測定した。なお△YはXYZ表示
のY値(明度に相当)を用い、初期テストピース状態と
所定期間暴露後のテストピースのY値の差を示し、数値
が大きくなるほどチョーキングが著しい。その結果を表
1に示す。
This sheet was placed in an oven at 190 ° C., a thermal stability test was conducted, and the time until blackening was measured. Also, a sheet prepared in the same manner was formed into a 1 mm thick sheet by a hot press at 185 ° C. and exposed outdoors. 12 months exposure,
The color of the test piece after 24 months and 30 months was measured and the degree of choking was measured by ΔY. It should be noted that ΔY uses the Y value (corresponding to the lightness) of XYZ display, and indicates the difference between the Y value of the initial test piece state and the Y value of the test piece after exposure for a predetermined period. The larger the value, the more remarkable the chalking. Table 1 shows the results.

【0019】比較例1〜7 ハイドロタルサイトの代わりにジブチルチンジラウレー
トを表1に示す部数で使用する以外は、実施例1〜10
と同様の配合で、同様の操作によりシートを作成し、熱
安定性試験と屋外暴露を行い、同様に黒化時間と△Yを
測定した。その結果を表1に示す。
Comparative Examples 1 to 7 Examples 1 to 10 except that dibutyltin dilaurate was used in the number shown in Table 1 instead of hydrotalcite.
A sheet was prepared with the same composition by the same operation as above, a thermal stability test and outdoor exposure were conducted, and the blackening time and ΔY were similarly measured. Table 1 shows the results.

【0020】[0020]

【表1】 [Table 1]

【0021】実施例11〜20 塩化ビニル樹脂100部、(重合度1100)ステアリ
ン酸カルシウム0.5部、ステアリン酸亜鉛0.5部、
ジブチルチンジマレート0.1部、弁柄1部及びカーボ
ンブラック0.1部に酢酸第一錫、o,o’−ジアルキ
ルジチオリン酸銅及びハイドロタルサイトを表2に記載
の部数で配合した。これを均一に分散混合した後、18
0℃の2本ロールで3分間混練し、暑さ1.5mmのシー
トを得た。
Examples 11 to 20 100 parts vinyl chloride resin, (polymerization degree 1100) 0.5 parts calcium stearate, 0.5 parts zinc stearate,
0.1 part of dibutyltin dimaleate, 1 part of rouge and 0.1 part of carbon black were mixed with stannous acetate, o, o′-dialkyldithiophosphate copper and hydrotalcite in the amounts shown in Table 2. After uniformly dispersing and mixing this,
The mixture was kneaded with two rolls at 0 ° C. for 3 minutes to obtain a sheet having a heat of 1.5 mm.

【0022】このシートを190℃のオーブン中に入
れ、熱安定性試験を行い、黒変するまでの時間を測定し
た。また同様に作成したシートを185℃の熱プレスで
1mm厚のシートに作成し屋外暴露した。暴露12ヶ月、
24ヶ月、30ヶ月後のテストピースを測色してチョー
キング度合いを△Eで測定した。なお△Eは、初期テス
トピース状態と所定期間暴露後のテストピースの色差を
示し、数値が大きくなるほどチョーキングが著しい。そ
の結果を表2に示す。
This sheet was placed in an oven at 190 ° C., a thermal stability test was conducted, and the time until blackening was measured. Also, a sheet prepared in the same manner was formed into a 1 mm thick sheet by a hot press at 185 ° C. and exposed outdoors. 12 months exposure,
After 24 months and 30 months, the color of the test piece was measured and the degree of choking was measured by ΔE. ΔE represents the color difference between the initial test piece state and the test piece after exposure for a predetermined period of time. The larger the value, the more marked the chalking. The results are shown in Table 2.

【0023】比較例8〜14 ハイドロタルサイト等を添加せず代わりにジブチルチン
ジマレートを場合により表2に記載の部数に増加させた
以外は、実施例11〜20と同様の配合で、同様の操作
によりシートを作成し、屋外暴露と熱安定性試験を行
い、同様に黒化時間と△Eを測定した。その結果を表2
に示す。
Comparative Examples 8 to 14 The same formulation as in Examples 11 to 20 except that hydrotalcite or the like was not added and dibutyltin dimaleate was optionally increased to the number shown in Table 2. A sheet was prepared by the above procedure, subjected to outdoor exposure and thermal stability test, and the blackening time and ΔE were similarly measured. The results are shown in Table 2.
Shown in

【0024】[0024]

【表2】 [Table 2]

【0025】[0025]

【発明の効果】本発明は以上の点から明かな如く、従来
のものと比較し、熱安定性がよく、長時間加熱成形加工
時の熱分解が防止され、しかも長期間にわたる成形品の
耐候性が優れ、特に成形品のチョーキングを著しく抑制
できる塩化ビニル樹脂組成物を提供し得る。
As is apparent from the above points, the present invention has better thermal stability than conventional ones, prevents thermal decomposition during long-time heat molding processing, and has a long-term weather resistance of molded products. It is possible to provide a vinyl chloride resin composition that has excellent properties and can significantly suppress choking of a molded product.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 塩化ビニル樹脂100重量部に対して、
o,o’−ジアルキルジチオリン酸銅及び/又は酢酸第
一錫の合計量で0.005〜1重量部、及びハイドロタ
ルサイト0.1〜3重量部含有することを特徴とする塩
化ビニル樹脂組成物。
[Claim 1] 100 parts by weight of a vinyl chloride resin,
Vinyl chloride resin composition containing 0.005 to 1 part by weight and 0.1 to 3 parts by weight of hydrotalcite as a total amount of o, o′-copper dialkyldithiophosphate and / or stannous acetate. Stuff.
【請求項2】 o,o’−ジアルキルジチオリン酸銅及
び/又は酢酸第一錫、及びハイドロタルサイトと着色成
分とを含有する請求項1記載の塩化ビニル樹脂組成物。
2. The vinyl chloride resin composition according to claim 1, which contains o, o'-dialkyldithiophosphate copper and / or stannous acetate, hydrotalcite and a coloring component.
JP22637495A 1995-09-04 1995-09-04 Vinyl chloride resin composition Pending JPH0967491A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22637495A JPH0967491A (en) 1995-09-04 1995-09-04 Vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22637495A JPH0967491A (en) 1995-09-04 1995-09-04 Vinyl chloride resin composition

Publications (1)

Publication Number Publication Date
JPH0967491A true JPH0967491A (en) 1997-03-11

Family

ID=16844137

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22637495A Pending JPH0967491A (en) 1995-09-04 1995-09-04 Vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPH0967491A (en)

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