JPH05140404A - Chlorinated vinyl chloride resin composition - Google Patents

Chlorinated vinyl chloride resin composition

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Publication number
JPH05140404A
JPH05140404A JP30922091A JP30922091A JPH05140404A JP H05140404 A JPH05140404 A JP H05140404A JP 30922091 A JP30922091 A JP 30922091A JP 30922091 A JP30922091 A JP 30922091A JP H05140404 A JPH05140404 A JP H05140404A
Authority
JP
Japan
Prior art keywords
vinyl chloride
chloride resin
chlorinated vinyl
thiodipropionate
resin composition
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
JP30922091A
Other languages
Japanese (ja)
Inventor
Tadashi Shinko
忠 新子
Hironobu Nakamura
裕信 中村
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical 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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP30922091A priority Critical patent/JPH05140404A/en
Publication of JPH05140404A publication Critical patent/JPH05140404A/en
Pending legal-status Critical Current

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Abstract

(57)【要約】 【構成】 ジステアリルチオジプロピオネート、ジベヘ
ニルチオジプロピオネートなどのチオジプロピオネート
が、塩素化塩化ビニル系樹脂100重量部に対して1〜
20重量部含有している塩素化塩化ビニル系樹脂組成
物。 【効果】 この塩素化塩化ビニル系樹脂組成物は、加熱
溶融時の流動性が良好で成形性がよく、耐熱性に優れて
いるので、耐熱性のよい製品を容易に成形することがで
きる。
(57) [Summary] [Structure] A thiodipropionate such as distearyl thiodipropionate or dibehenyl thiodipropionate is contained in an amount of 1 to 100 parts by weight of a chlorinated vinyl chloride resin.
A chlorinated vinyl chloride resin composition containing 20 parts by weight. [Effect] Since this chlorinated vinyl chloride resin composition has good fluidity during heating and melting, good moldability, and excellent heat resistance, a product having good heat resistance can be easily molded.

Description

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

【0001】[0001]

【産業上の利用分野】この発明は、溶融時の流動性がよ
く成形性に優れた塩素化塩化ビニル系樹脂組成物に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a chlorinated vinyl chloride resin composition having good fluidity when melted and excellent in moldability.

【0002】[0002]

【従来の技術】塩素化塩化ビニル系樹脂は、一般に塩化
ビニル系樹脂を塩素化して製造されており、塩化ビニル
系樹脂の長所である難燃性、耐水性、耐薬品性、耐候性
等の優れた特性を有している上、熱変形温度が20〜4
0℃向上しているという利点をもっている。
2. Description of the Related Art Chlorinated vinyl chloride resin is generally produced by chlorinating vinyl chloride resin, and has the advantages of vinyl chloride resin such as flame resistance, water resistance, chemical resistance and weather resistance. It has excellent properties and a heat distortion temperature of 20-4.
It has the advantage of being improved by 0 ° C.

【0003】従って、耐熱性の要求される用途への展開
が期待されているが、耐熱性が優れている反面、加熱溶
融時の流動性が悪く成形性に劣るという欠点を有してお
り、この成形性を改良するために、可塑剤や滑剤などの
流動性改良剤を添加することなど、種々の提案がされて
いる。
Therefore, although it is expected to be applied to applications in which heat resistance is required, it has excellent heat resistance, but on the other hand, it has the drawback of poor flowability during heating and melting and poor moldability. In order to improve the moldability, various proposals have been made such as adding a fluidity improver such as a plasticizer or a lubricant.

【0004】例えば、特開平2−113048号公報に
は、塩化含有ビニル系樹脂に次式(2)で表される可塑
剤を添加することが提案されている。
For example, Japanese Patent Application Laid-Open No. 2-113048 proposes to add a plasticizer represented by the following formula (2) to a chloride-containing vinyl resin.

【0005】[0005]

【化2】 [Chemical 2]

【0006】(式中、t、mは1又は2の整数、R1
2は炭素数4〜13の直鎖又は分岐のアルキル基を示
す。)
(Where, t and m are integers of 1 or 2, R 1 ,
R 2 represents a linear or branched alkyl group having 4 to 13 carbon atoms. )

【0007】[0007]

【発明が解決しようとする課題】しかし、上式(2)の
化合物からなる可塑剤は融点が低く、また、分子鎖長が
さほど長くないため、加熱溶融時の流動性は向上したと
しても、耐熱性の低下が著しくなるという問題点を有し
ている。
However, since the plasticizer comprising the compound of the above formula (2) has a low melting point and the molecular chain length is not so long, even if the fluidity at the time of heating and melting is improved, There is a problem that the heat resistance is significantly lowered.

【0008】この発明は、上記の点に鑑み、耐熱性の低
下が少なく、加熱溶融時の流動性が良好な塩素化塩化ビ
ニル系樹脂組成物を提供することを目的とする。
In view of the above points, an object of the present invention is to provide a chlorinated vinyl chloride resin composition having a small decrease in heat resistance and a good fluidity during heating and melting.

【0009】[0009]

【課題を解決するための手段】この発明の塩素化塩化ビ
ニル系樹脂組成物は、次式(1)で表されるチオジプロ
ピオネートが塩素化塩化ビニル系樹脂を主体とする樹脂
100重量部に対して1〜20重量部含有されているこ
とを特徴とする。
The chlorinated vinyl chloride resin composition of the present invention comprises 100 parts by weight of a resin whose thiodipropionate represented by the following formula (1) is mainly a chlorinated vinyl chloride resin. 1 to 20 parts by weight is contained.

【0010】[0010]

【化3】 [Chemical 3]

【0011】(式中、R1 、R2 は炭素数14〜28の
直鎖又は分岐のアルキル基を示す。) この発明で使用される塩素化塩化ビニル系樹脂は、塩化
ビニル系樹脂を後塩素化した樹脂であり、塩化ビニルの
単独重合体を後塩素化して得られたものに限らず、塩化
ビニルと他の単量体との共重合体を後塩素化したもので
あってもよく、その塩素含有率は60〜72重量%、好
ましくは62〜69重量%である。塩素含有率が60重
量%未満であったり、72重量%を超えると、上記のチ
オジプロピオネートと混ざり難くなって、ブリードアウ
ト等の成形不良が生ずるからである。
(In the formula, R 1 and R 2 represent a linear or branched alkyl group having 14 to 28 carbon atoms.) The chlorinated vinyl chloride resin used in the present invention is a vinyl chloride resin. It is a chlorinated resin and is not limited to one obtained by post-chlorinating a vinyl chloride homopolymer, but may be one obtained by post-chlorinating a copolymer of vinyl chloride and another monomer. Its chlorine content is 60 to 72% by weight, preferably 62 to 69% by weight. This is because if the chlorine content is less than 60% by weight or exceeds 72% by weight, it becomes difficult to mix with the above-mentioned thiodipropionate, and molding defects such as bleeding out occur.

【0012】そして、塩素化塩化ビニル系樹脂の重合度
は特に限定されないが、平均重合度が300〜1500
の範囲のものが好適に使用される。平均重合度が300
未満であると得られる成形体の破断伸びなどの機械的物
性が低下し、1500を超えると、溶融時の流動性が悪
くなり、上記チオジプロピオネートと混ざり難くなるか
らである。
The degree of polymerization of the chlorinated vinyl chloride resin is not particularly limited, but the average degree of polymerization is 300 to 1500.
Those in the range of are preferably used. Average degree of polymerization is 300
If it is less than 1, the mechanical properties such as elongation at break of the obtained molded article will be deteriorated, and if it exceeds 1500, the fluidity at the time of melting will be deteriorated and it will be difficult to mix with the thiodipropionate.

【0013】また、組成物中の樹脂分としては、塩素化
塩化ビニル系樹脂単独のみならず、塩化ビニル系樹脂な
どが配合されていてもよい。この場合、樹脂混合物の塩
素含有率は60〜72重量%であることが好ましい。樹
脂混合物中の塩素含有率が60重量%未満であると、耐
熱性の向上が十分でないからである。
As the resin component in the composition, not only the chlorinated vinyl chloride resin alone but also the vinyl chloride resin may be blended. In this case, the chlorine content of the resin mixture is preferably 60 to 72% by weight. This is because when the chlorine content in the resin mixture is less than 60% by weight, the heat resistance is not sufficiently improved.

【0014】この発明で使用されるチオジプロピオネー
トは、上記の式(1)で表されるものであって、式中、
1 、R2 で示される直鎖又は分岐のアルキル基の炭素
数が14〜28とされるのは、R1 、R2 の炭素数が1
3以下であると得られる成形体の機械的強度が低下し、
かつ耐熱性を大幅に低下するからであり、R1 、R2
炭素数が29以上であると、そのチオジプロピオネート
は塩素化塩化ビニル系樹脂に対しての滑性が強くなりす
ぎて混合困難となるからである。
The thiodipropionate used in the present invention is represented by the above formula (1), wherein:
R 1, the number of carbon atoms in the straight-chain or branched alkyl group represented by R 2 is a 14-28 has a carbon number of R 1, R 2 is 1
If it is 3 or less, the mechanical strength of the obtained molded article decreases,
In addition, the heat resistance is significantly reduced, and when the carbon number of R 1 and R 2 is 29 or more, the thiodipropionate becomes too slippery with respect to the chlorinated vinyl chloride resin. This is because mixing becomes difficult.

【0015】そして、このチオジプロピオネートとして
は、一般にR1 、R2 が同一のアルキル基で示されるも
のであって、例えば、ジミリスチルチオジプロピオネー
ト(アルキル基の炭素数14)、ジパルミチルチオジプ
ロピオネート(アルキル基の炭素数16)、ジステアリ
ルチオジプロピオネート(アルキル基の炭素数18)、
ジベヘニルチオジプロピオネート(アルキル基の炭素数
22)、ジセロチルチオジプロピオネート(アルキル基
の炭素数26)などがあげられ、特に、ジパルミチルチ
オジプロピオネート、ジステアリルチオジプロピオネー
ト及びジベヘニルチオジプロピオネートが好適に使用さ
れる。
The thiodipropionate is generally one in which R 1 and R 2 are the same alkyl group, and examples thereof include dimyristyl thiodipropionate (alkyl group having 14 carbon atoms), Palmityl thiodipropionate (alkyl group having 16 carbon atoms), distearyl thiodipropionate (alkyl group having 18 carbon atoms),
Examples thereof include dibehenyl thiodipropionate (alkyl group having 22 carbon atoms) and dicerotyl thiodipropionate (alkyl group having 26 carbon atoms). Particularly, dipalmityl thiodipropionate and distearyl thiodipropionate And dibehenyl thiodipropionate are preferably used.

【0016】このチオジプロピオネートは、上記のとお
り、塩素化塩化ビニル系樹脂を主体とする樹脂100重
量部(樹脂分が塩素化塩化ビニル系樹脂のみの場合に
は、塩素化塩化ビニル系樹脂100重量部)に対して1
〜20重量部とされるが、より好ましくは3〜10重量
部である。1重量部未満であると溶融時の流動性の向上
が殆ど見られず、20重量部を超える場合には樹脂と混
和し難くなるからである。
This thiodipropionate is, as described above, 100 parts by weight of a resin mainly containing a chlorinated vinyl chloride resin (when the resin content is only a chlorinated vinyl chloride resin, the chlorinated vinyl chloride resin is 1 to 100 parts by weight)
The amount is ˜20 parts by weight, more preferably 3 to 10 parts by weight. This is because if it is less than 1 part by weight, the fluidity at the time of melting is hardly improved, and if it exceeds 20 parts by weight, it becomes difficult to mix with the resin.

【0017】この発明の塩素化塩化ビニル系樹脂組成物
には、その物性に好ましくない影響を与えない範囲で、
従来から使用されている熱安定剤、滑剤、加工助剤、酸
化防止剤、改質剤、充填剤、紫外線吸収剤、着色剤など
が併用添加される。
The chlorinated vinyl chloride resin composition of the present invention can be used in an amount not adversely affecting the physical properties of the resin composition.
Conventionally used heat stabilizers, lubricants, processing aids, antioxidants, modifiers, fillers, UV absorbers, colorants and the like are added together.

【0018】例えば、熱安定剤としては、オクチル錫マ
レート、ジメチル錫メルカプト、ジブチル錫マレートな
どの有機錫系安定剤、二塩基性ステアリン酸鉛、三塩基
性硫酸鉛、ステアリン酸鉛などの鉛系安定剤、バリウム
−亜鉛、カルシウム−亜鉛などの複合安定剤及び無機安
定剤などがあげられる。滑剤としては、ステアリルアル
コール、ポリエチレンワックス、ステアリン酸カルシウ
ム、ブチルステアレート、エステル系滑剤などがあげら
れる。
For example, as the heat stabilizer, organotin stabilizers such as octyl tin malate, dimethyl tin mercapto and dibutyl tin malate, lead bases such as dibasic lead stearate, tribasic lead sulfate and lead stearate. Examples include stabilizers, composite stabilizers such as barium-zinc and calcium-zinc, and inorganic stabilizers. Examples of lubricants include stearyl alcohol, polyethylene wax, calcium stearate, butyl stearate, and ester lubricants.

【0019】また、改質剤としては、塩素化ポリエチレ
ン、エチレン−酢酸ビニル共重合体、アクリルニトリル
−ブタジエン−スチレンラバー、メチルメタクリレート
−ブタジエン−スチレンラバーなどの衝撃改質剤などが
あげられ、酸化防止剤としは、ビスフェノールA、ブチ
ルヒドロキシトルエンなどがあげられ、充填剤として
は、ガラス繊維、炭酸カルシウム、タルクなどがあげら
れ、紫外線吸収剤としては、サリシレートエステル、ベ
ンゾエートエステル、ベンゾフェノン系紫外線吸収剤、
ベンゾトリアゾール系紫外線吸収剤などがあげられる。
Examples of the modifier include impact modifiers such as chlorinated polyethylene, ethylene-vinyl acetate copolymer, acrylonitrile-butadiene-styrene rubber and methylmethacrylate-butadiene-styrene rubber. Examples of the inhibitor include bisphenol A, butyl hydroxytoluene, etc., examples of the filler include glass fiber, calcium carbonate, talc, etc., and examples of the ultraviolet absorber include salicylate ester, benzoate ester, benzophenone ultraviolet absorber. ,
Examples thereof include benzotriazole-based ultraviolet absorbers.

【0020】そして、この発明の塩素化塩化ビニル系樹
脂組成物の成形には、射出成形、押出成形、カレンダー
成形、ロ−ル・プレス成形等従来の公知の成形法が適宜
採用される。
For molding the chlorinated vinyl chloride resin composition of the present invention, conventionally known molding methods such as injection molding, extrusion molding, calender molding and roll press molding are appropriately adopted.

【0021】[0021]

【実施例】次に、この発明の実施例を説明する。以下、
部とあるのは重量部を意味する。実施例1〜6、比較例1〜4 樹脂として、表1に示したとおり、二種類の塩素化塩化
ビニル系樹脂(塩素含有率64重量%、平均重合度50
0の塩素化塩化ビニル系樹脂;塩素化塩化ビニル系樹脂
A、塩素含有率68重量%、平均重合度1000の塩素
化塩化ビニル系樹脂;塩素化塩化ビニル系樹脂B)及び
塩素含有率56.8重量%、平均重合度500の塩化ビ
ニル樹脂を使用した。
Embodiments of the present invention will be described below. Less than,
Parts means parts by weight. Examples 1 to 6 and Comparative Examples 1 to 4, as shown in Table 1, two kinds of chlorinated vinyl chloride resins (chlorine content 64% by weight, average degree of polymerization 50)
0. chlorinated vinyl chloride-based resin; chlorinated vinyl chloride-based resin A, chlorine content 68 weight%, average polymerization degree 1000 chlorinated vinyl chloride-based resin; chlorinated vinyl chloride-based resin B) and chlorine content 56. A vinyl chloride resin having 8% by weight and an average degree of polymerization of 500 was used.

【0022】また、チオジプロピオネートとして、表1
に示したとおり、ジステアリルチオジプロピオネート
(Rの炭素数18)、ジベヘニルチオジプロピオネート
(アルキル基の炭素数22)、ジラウリルチオジプロピ
オネート(アルキル基の炭素数12;比較例)を使用し
た。
Further, as thiodipropionate, Table 1
As shown in FIG. 4, distearyl thiodipropionate (R has 18 carbon atoms), dibehenyl thiodipropionate (alkyl group has 22 carbon atoms), dilauryl thiodipropionate (alkyl group has 12 carbon atoms; Comparative Example )It was used.

【0023】その他の配合物として、表1に示すとおり
の熱安定剤、滑剤等の添加物を使用した。上記の樹脂、
チオジプロピオネート、その他の添加物を表1に示すと
おりの割合で添加し、それぞれの樹脂組成物をヘンシェ
ルミキサーに供給し、約80℃、5分間混合した。その
後、190℃のロールで3分間溶融混練した。
As other compounds, additives such as heat stabilizers and lubricants as shown in Table 1 were used. The above resin,
Thiodipropionate and other additives were added in the proportions shown in Table 1, and the respective resin compositions were supplied to a Henschel mixer and mixed at about 80 ° C. for 5 minutes. Then, the mixture was melt-kneaded with a roll at 190 ° C. for 3 minutes.

【0024】樹脂組成物の溶融時の流動性を見るため、
得られたそれぞれの混練物を高化式フローテスターに供
給し、直径1mm、長さ10mmのダイを用い、荷重1
60kgf/cm2 、温度180℃における単位時間の
吐出量(×10-2cc/sec)を測定した。
In order to check the fluidity of the resin composition at the time of melting,
Each of the obtained kneaded products was supplied to a Koka type flow tester, and a die having a diameter of 1 mm and a length of 10 mm was used to apply a load of 1
The discharge rate (× 10 -2 cc / sec) per unit time at 60 kgf / cm 2 and a temperature of 180 ° C. was measured.

【0025】また、樹脂組成物による成形体の耐熱性を
見るため、得られた混練物を、190℃、150kg/
cm2 でプレス成形して試験片を作成した。この試験片
について、JIS−K−7207に準拠(荷重18.5
kgf/cm2 )して荷重たわみ温度測定(℃)を行っ
た。
Further, in order to check the heat resistance of the molded product made of the resin composition, the obtained kneaded product was heated at 190 ° C. and 150 kg /
A test piece was prepared by press molding at cm 2 . This test piece complies with JIS-K-7207 (load 18.5).
kgf / cm 2) and heat deflection temperature measured (℃) was carried out.

【0026】吐出量測定の結果及び荷重たわみ温度測定
の結果は表1に示したとおりであった。
The results of discharge amount measurement and deflection temperature under load are shown in Table 1.

【0027】[0027]

【表1】 [Table 1]

【0028】上記の結果から明らかなとおり、この発明
の塩素化塩化ビニル系樹脂組成物は、加熱溶融時の流動
性がよく、かつ耐熱性にも優れている。
As is apparent from the above results, the chlorinated vinyl chloride resin composition of the present invention has good fluidity when heated and melted and also has excellent heat resistance.

【0029】[0029]

【発明の効果】この発明の塩素化塩化ビニル系樹脂組成
物は、以上述べたとおりであり、加熱溶融時の流動性が
よく、耐熱性に優れているので、耐熱性のよい製品を容
易に成形することができる。
As described above, the chlorinated vinyl chloride resin composition of the present invention has good fluidity during heating and melting and excellent heat resistance. It can be molded.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 次式(1)で表されるチオジプロピオ
ネートが塩素化塩化ビニル系樹脂を主体とする樹脂10
0重量部に対して1〜20重量部含有されていることを
特徴とする塩素化塩化ビニル系樹脂組成物。 【化1】 (式中、R1 、R2 は炭素数14〜28の直鎖又は分岐
のアルキル基を示す。)
1. A resin 10 in which a thiodipropionate represented by the following formula (1) is mainly a chlorinated vinyl chloride resin.
A chlorinated vinyl chloride resin composition, which is contained in an amount of 1 to 20 parts by weight based on 0 parts by weight. [Chemical 1] (In the formula, R 1 and R 2 represent a linear or branched alkyl group having 14 to 28 carbon atoms.)
JP30922091A 1991-11-25 1991-11-25 Chlorinated vinyl chloride resin composition Pending JPH05140404A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP30922091A JPH05140404A (en) 1991-11-25 1991-11-25 Chlorinated vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP30922091A JPH05140404A (en) 1991-11-25 1991-11-25 Chlorinated vinyl chloride resin composition

Publications (1)

Publication Number Publication Date
JPH05140404A true JPH05140404A (en) 1993-06-08

Family

ID=17990382

Family Applications (1)

Application Number Title Priority Date Filing Date
JP30922091A Pending JPH05140404A (en) 1991-11-25 1991-11-25 Chlorinated vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPH05140404A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6306950B1 (en) 1997-12-03 2001-10-23 Kaneka Corporation Chlorinated vinyl chloride resin composition
JP2005276699A (en) * 2004-03-25 2005-10-06 Asahi Denka Kogyo Kk Wire coating material composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6306950B1 (en) 1997-12-03 2001-10-23 Kaneka Corporation Chlorinated vinyl chloride resin composition
JP2005276699A (en) * 2004-03-25 2005-10-06 Asahi Denka Kogyo Kk Wire coating material composition

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