JP2001234017A - Chlorinated vinyl chloride-based resin composition - Google Patents

Chlorinated vinyl chloride-based resin composition

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Publication number
JP2001234017A
JP2001234017A JP2000047895A JP2000047895A JP2001234017A JP 2001234017 A JP2001234017 A JP 2001234017A JP 2000047895 A JP2000047895 A JP 2000047895A JP 2000047895 A JP2000047895 A JP 2000047895A JP 2001234017 A JP2001234017 A JP 2001234017A
Authority
JP
Japan
Prior art keywords
vinyl chloride
chlorinated vinyl
parts
chloride resin
weight
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
JP2000047895A
Other languages
Japanese (ja)
Inventor
Tsuyoshi Suzuki
毅之 鈴木
Minoru Isshiki
実 一色
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.)
Kanegafuchi Chemical Industry Co Ltd
Original Assignee
Kanegafuchi 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 Kanegafuchi Chemical Industry Co Ltd filed Critical Kanegafuchi Chemical Industry Co Ltd
Priority to JP2000047895A priority Critical patent/JP2001234017A/en
Publication of JP2001234017A publication Critical patent/JP2001234017A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To provide a chlorinated vinyl chloride-based resin composition which maintains a tensile strength at high temperature, has a large impact-resistant strength at low temperature, and is used for molding. SOLUTION: This chlorinated vinyl chloride-based resin composition which comprises 100 pts.wt. of a chlorinated vinyl chloride-based resin having a mol.wt. of 600 to 1,500 before chlorinated and having a chlorination degree of 62 to 70 wt.%, 2 to 8 pts.wt. of a polyorganosiloxane and 1 to 5 wt.% of an acrylic modifier resin.

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、塩素化塩化ビニル
系樹脂組成物、特に低温での耐衝撃強度が強く、高温で
の引張強度が強い成形用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, and more particularly to a molding chlorinated vinyl chloride resin composition having high impact strength at low temperatures and high tensile strength at high temperatures.

【0002】[0002]

【従来の技術】塩素化塩化ビニル系樹脂の成形物は、耐
熱性が高いという特徴を有し、従来の塩化ビニル系樹脂
の成形物では加熱変形するために使用できないような比
較的高温での用途に用いられている。例えば、塩化ビニ
ル系樹脂成形物よりも熱変形温度が20〜40℃も高い
ことを利用して、熱水用パイプとして塩素化塩化ビニル
系樹脂成形物が用いられる。あるいは、塩化ビニル系樹
脂成形物よりも熱変形温度が高いことを利用して、熱の
かかる家電用のシートとして塩素化塩化ビニル系樹脂成
形物が用いられる。一方、塩素化塩化ビニル系樹脂の成
形物は、高温での引張強度が強い反面で、低温での耐衝
撃性が弱いことが知られている。この低温での耐衝撃性
が弱いことを克服するために、塩素化塩化ビニル系樹脂
組成物においてABS,MBS等の耐衝撃改良剤を配合
することが知られている。これらの耐衝撃吸収剤は低温
での耐衝撃性を向上するものの十分ではなかった。この
問題を解決するために、特公昭49−18102では、
塩素化塩化ビニル系樹脂組成物において、ABS及び/
又はMBSと塩素化ポリエチレンを配合することを提案
している。しかし、塩素化塩化ビニル系樹脂組成物に塩
素化ポリエチレンを配合することで耐衝撃性は優れて改
善されるものの、塩素化塩化ビニル系樹脂成形物の軟化
温度が下がり、高温での引張強度が低下する問題があっ
た。この軟化温度の低下および高温での引張強度の低下
を最小限に防ぐため、塩素化ポリエチレンを配合しても
配合量を2〜4部と最小限に抑えることが必要であり、
低温での耐衝撃性の向上が十分でなく、塩素化塩化ビニ
ル系樹脂組成物としては不十分なものであった。
2. Description of the Related Art A molded article of a chlorinated vinyl chloride resin has a feature of high heat resistance, and is used at a relatively high temperature at which a conventional molded article of a vinyl chloride resin cannot be used due to heat deformation. Used for applications. For example, a chlorinated vinyl chloride resin molded article is used as a pipe for hot water, utilizing the fact that the heat distortion temperature is higher by 20 to 40 ° C. than that of a vinyl chloride resin molded article. Alternatively, a chlorinated vinyl chloride-based resin molded product is used as a sheet for household appliances to which heat is applied, utilizing the fact that the heat deformation temperature is higher than that of the vinyl chloride-based resin molded product. On the other hand, it is known that a molded article of a chlorinated vinyl chloride resin has a high tensile strength at a high temperature, but has a low impact resistance at a low temperature. In order to overcome the low impact resistance at low temperatures, it is known to incorporate an impact modifier such as ABS or MBS into a chlorinated vinyl chloride resin composition. These shock absorbers improve the impact resistance at low temperatures but are not satisfactory. In order to solve this problem, Japanese Patent Publication No.
In the chlorinated vinyl chloride resin composition, ABS and / or
Alternatively, it has been proposed to mix MBS and chlorinated polyethylene. However, although the impact resistance is improved and improved by blending chlorinated polyethylene with the chlorinated vinyl chloride resin composition, the softening temperature of the chlorinated vinyl chloride resin molded product decreases, and the tensile strength at high temperatures decreases. There was a problem of lowering. In order to minimize the decrease in the softening temperature and the decrease in the tensile strength at a high temperature, it is necessary to minimize the blending amount to 2 to 4 parts even when the chlorinated polyethylene is blended,
The impact resistance at low temperatures was not sufficiently improved, and was insufficient as a chlorinated vinyl chloride resin composition.

【0003】[0003]

【発明が解決しようとする課題】本発明の目的は、高温
での引張強度を維持し、低温での耐衝撃性に優れる、好
ましい塩素化塩化ビニル系樹脂組成物を提供することに
ある。
SUMMARY OF THE INVENTION An object of the present invention is to provide a preferable chlorinated vinyl chloride resin composition which maintains tensile strength at a high temperature and has excellent impact resistance at a low temperature.

【0004】[0004]

【課題を解決するための手段】本発明は、上記の目的を
達成するために、塩素化前の重合度が600〜1500
であり、塩素化度が62〜70重量%である塩素化塩化
ビニル系樹脂100重量部とポリオルガノシロキサン2
〜8重量部およびアクリル系モディファイヤー樹脂1〜
5重量部を含んでなる塩素化塩化ビニル系樹脂組成物を
提供する。
According to the present invention, in order to achieve the above object, the degree of polymerization before chlorination is from 600 to 1500.
And 100 parts by weight of a chlorinated vinyl chloride resin having a chlorination degree of 62 to 70% by weight and polyorganosiloxane 2
~ 8 parts by weight and acrylic modifier resin 1 ~
A chlorinated vinyl chloride resin composition comprising 5 parts by weight.

【0005】[0005]

【発明の実施の形態】本発明で用いられる塩素化塩化ビ
ニル系樹脂の原料である塩素化前の塩化ビニル系樹脂の
平均重合度は、600から1500,好ましくは600
〜1300、より好ましくは600〜1200であり、
塩素化塩化ビニル系樹脂の塩素化度は62〜70重量
%、好ましくは63〜70重量%、より好ましくは64
〜70重量%である。塩素化塩化ビニル系樹脂の原料で
ある塩化ビニル系樹脂の平均重合度が600未満であれ
ば、十分な機械的強度が得られず、一方、その重合度が
1500を越えると、樹脂組成物の加工が容易でないの
で好ましくない。塩素化塩化ビニル系樹脂の塩素化度が
62重量%未満であれば、十分な耐熱性を有する組成物
が得られず、一方、塩素化度が70重量%を越えると、
溶融粘度が高くなり、樹脂組成物の加工に技術的な困難
を伴うので、好ましくない。本発明において「塩化ビニ
ル系樹脂」は、塩化ビニルの単独重合体、および塩化ビ
ニルと他の共重合可能な単量体、例えば、エチレン、プ
ロピレン、酢酸ビニル、塩化アリル、アリルグリシジル
エーテル、アクリル酸エステル、ビニルエーテル等との
共重合体を包含する。
BEST MODE FOR CARRYING OUT THE INVENTION The average degree of polymerization of a vinyl chloride resin before chlorination, which is a raw material of the chlorinated vinyl chloride resin used in the present invention, is from 600 to 1500, preferably from 600.
~ 1300, more preferably from 600 to 1200,
The chlorination degree of the chlorinated vinyl chloride resin is 62 to 70% by weight, preferably 63 to 70% by weight, more preferably 64 to 70% by weight.
7070% by weight. If the average degree of polymerization of the vinyl chloride resin as a raw material of the chlorinated vinyl chloride resin is less than 600, sufficient mechanical strength cannot be obtained, while if the degree of polymerization exceeds 1500, It is not preferable because processing is not easy. When the chlorination degree of the chlorinated vinyl chloride resin is less than 62% by weight, a composition having sufficient heat resistance cannot be obtained. On the other hand, when the chlorination degree exceeds 70% by weight,
It is not preferable because the melt viscosity becomes high and processing of the resin composition involves technical difficulties. In the present invention, "vinyl chloride resin" is a homopolymer of vinyl chloride, and other copolymerizable monomers with vinyl chloride, for example, ethylene, propylene, vinyl acetate, allyl chloride, allyl glycidyl ether, acrylic acid Includes copolymers with esters, vinyl ethers and the like.

【0006】本発明で、ポリオルガノシロキサンとして
は、シリコンゴムを含有する有機化合物であって、メチ
ルメタクリレートをグラフトしているものが好ましい。
このようなポリオルガノシロキサンとして、三菱レーヨ
ン社製のS2001が知られている。
In the present invention, the polyorganosiloxane is preferably an organic compound containing a silicone rubber and grafted with methyl methacrylate.
As such a polyorganosiloxane, S2001 manufactured by Mitsubishi Rayon Co., Ltd. is known.

【0007】ポリオルガノシロキサンの配合量が2重量
部未満だと成形品の耐衝撃物性が低下し、8重量部を越
えると塩素化塩化ビニル系樹脂の持つ特性である耐熱性
が低下する。本発明の塩素化塩化ビニル系樹脂組成物
は、上記ポリオルガノシロキサンに加えてアクリル系モ
ディファイヤー樹脂1〜5重量部を含んでなることを特
徴とする。ポリオルガノシロキサン単独では、上記の低
温での耐衝撃強度が十分満足できない。
[0007] If the amount of the polyorganosiloxane is less than 2 parts by weight, the impact resistance of the molded article is reduced. The chlorinated vinyl chloride resin composition of the present invention is characterized in that it contains 1 to 5 parts by weight of an acrylic modifier resin in addition to the polyorganosiloxane. The polyorganosiloxane alone cannot sufficiently satisfy the above-mentioned impact strength at low temperatures.

【0008】上記のアクリル系モディファイヤー樹脂と
しては、アルキルアクリレートモノマーを重合した樹脂
であり、特にアルキルアクリレート樹脂にアルキルメタ
アクリレートがグラフト重合した樹脂が好ましく用いら
れる。また、アクリル系モディフィヤー樹脂として、ブ
タジエン成分を20重量%以下の範囲で含んでもよい。
本発明で用いられるアクリル系モディファイヤー樹脂と
して鐘淵化学工業株式会社製の商品名FM−10,FM
−20,FT−80が知られており、またRohm &
Haas社製の商品名KM334,KM365,KM
330などがある。用いるアクリル系モディファイヤー
樹脂の配合量が1重量部未満であると、成形品の目的と
する低温での耐衝撃性が満足されない。また、用いるの
アクリル系モディファイヤー樹脂の配合量が5重量部以
上であると、成形品の高温での引張強度が不十分とな
る。
The acrylic modifier resin is a resin obtained by polymerizing an alkyl acrylate monomer, and particularly preferably a resin obtained by graft-polymerizing an alkyl acrylate resin with an alkyl methacrylate. The acrylic modifier resin may contain a butadiene component in a range of 20% by weight or less.
As the acrylic modifier resin used in the present invention, trade names FM-10 and FM manufactured by Kaneka Chemical Industry Co., Ltd.
-20 and FT-80 are known, and Rohm &
Product name KM334, KM365, KM manufactured by Haas
330 and the like. If the amount of the acrylic modifier resin used is less than 1 part by weight, the intended low-temperature impact resistance of the molded product is not satisfied. On the other hand, if the amount of the acrylic modifier resin used is 5 parts by weight or more, the tensile strength of the molded product at a high temperature becomes insufficient.

【0009】[0009]

【実施例】以下に実施例および比較例を挙げて本発明を
具体的に説明する。しかし、本発明はこれらに限定され
るものではない。尚、実施例および比較例中、「部」お
よび「%」は、特に記載のない限り、それぞれ「重量
部」および「重量%」を表す。
The present invention will be specifically described below with reference to examples and comparative examples. However, the present invention is not limited to these. In Examples and Comparative Examples, "parts" and "%" represent "parts by weight" and "% by weight", respectively, unless otherwise specified.

【0010】(実施例1)重合度1000の塩化ビニル
樹脂を後塩素化して塩素化度が67%の塩素化塩化ビニ
ル樹脂を得た。この塩素化塩化ビニル樹脂100部に、
衝撃吸収剤としてS2001(三菱レーヨン社製のポリ
オルガノシロキサン)5重量部とFM−10(鐘淵化学
工業株式会社のアクリル系モディファイヤー樹脂)4部
および安定剤としてブチル錫系安定剤2部、安定化助剤
として合成ゼオライトを0.5部、滑剤を2部、充填剤
として二酸化チタン4.5部を加えた。この配合物のハ
ンドブレンドをおこない均一な配合物を得た。
(Example 1) A vinyl chloride resin having a polymerization degree of 1000 was post-chlorinated to obtain a chlorinated vinyl chloride resin having a chlorination degree of 67%. 100 parts of this chlorinated vinyl chloride resin
5 parts by weight of S2001 (polyorganosiloxane manufactured by Mitsubishi Rayon Co., Ltd.) and 4 parts of FM-10 (acrylic modifier resin manufactured by Kanebuchi Chemical Industry Co., Ltd.) as a shock absorber and 2 parts of a butyltin-based stabilizer as a stabilizer, 0.5 parts of synthetic zeolite, 2 parts of lubricant and 4.5 parts of titanium dioxide as filler were added as a stabilizing aid. The blend was hand blended to obtain a uniform blend.

【0011】このブレンド配合物を、200℃の8イン
チのロールにて3分間混練し、205℃のプレス機にて
10分間プレス後に切削して試験片を得た。JIS K
7110に準じて−7℃でのアイゾット衝撃試験をお
こなったところアイゾット衝撃試験値は10.6kg・
cm/cm2であった。また、JIS K 7113に
準じて82℃での引張試験をおこなったところ、引張強
度は246kg/cm 2であった。また、JIS K
7206に準じた5kg荷重でのVicat軟化点は1
17.4℃だった。
[0011] The blend formulation is treated at 200 ° C with 8 inches.
And kneaded for 3 minutes with a roll of
A test piece was obtained by cutting after pressing for 10 minutes. JIS K
 Izod impact test at -7 ° C according to 7110
At this point, the Izod impact test value was 10.6 kg
cm / cmTwoMet. In addition, JIS K 7113
When a tensile test was conducted at 82 ° C.
The degree is 246kg / cm TwoMet. Also, JIS K
Vicat softening point at 5 kg load according to 7206 is 1
17.4 ° C.

【0012】(実施例2)重合度1000の塩化ビニル
樹脂を後塩素化して塩素化度が67%の塩素化塩化ビニ
ル樹脂を得た。この塩素化塩化ビニル樹脂100部に、
衝撃吸収剤としてS2001(三菱レーヨン社製のポリ
オルガノシロキサン)5重量部とFM−20(鐘淵化学
工業株式会社のアクリル系モディファイヤー樹脂)4部
および安定剤としてブチル錫系安定剤2部、安定化助剤
として合成ゼオライトを0.5部、滑剤を2部、充填剤
として二酸化チタン4.5部を加えた。この配合物のハ
ンドブレンドをおこない均一な配合物を得た。
Example 2 A vinyl chloride resin having a degree of polymerization of 1000 was post-chlorinated to obtain a chlorinated vinyl chloride resin having a degree of chlorination of 67%. 100 parts of this chlorinated vinyl chloride resin
5 parts by weight of S2001 (polyorganosiloxane manufactured by Mitsubishi Rayon Co., Ltd.) and 4 parts of FM-20 (acrylic modifier resin manufactured by Kanebuchi Chemical Industry Co., Ltd.) as a shock absorber and 2 parts of a butyltin-based stabilizer as a stabilizer, 0.5 parts of synthetic zeolite, 2 parts of lubricant and 4.5 parts of titanium dioxide as filler were added as a stabilizing aid. The blend was hand blended to obtain a uniform blend.

【0013】このブレンド配合物を、200℃の8イン
チのロールにて3分間混練し、205℃のプレス機にて
10分間プレス後に切削して試験片を得た。JIS K
7110に準じて−7℃でのアイゾット衝撃試験をお
こなったところアイゾット衝撃試験値は9.2kg・c
m/cm2であった。また、JIS K 7113に準
じて82℃での引張試験をおこなったところ、引張強度
は242kg/cm2であった。また、JIS K 7
206に準じた5kg荷重でのVicat軟化点は11
7.9℃だった。
The blend was kneaded with an 8-inch roll at 200 ° C. for 3 minutes, pressed with a press machine at 205 ° C. for 10 minutes, and then cut to obtain a test piece. JIS K
When an Izod impact test at -7 ° C. was performed according to 7110, the Izod impact test value was 9.2 kg · c.
m / cm 2 . In addition, when a tensile test was performed at 82 ° C. according to JIS K 7113, the tensile strength was 242 kg / cm 2 . In addition, JIS K7
The Vicat softening point at 5 kg load according to 206 is 11
7.9 ° C.

【0014】(比較例1)重合度1000の塩化ビニル
樹脂を後塩素化して塩素化度が67%の塩素化塩化ビニ
ル樹脂を得た。この塩素化塩化ビニル樹脂100部に、
衝撃吸収剤としてブタジエン含有量46%のB22(鐘
淵化学工業株式会社製のMBS)6部と塩素含有量36
%の塩素化ポリエチレンTyrin3615P(デュポ
ン ダウ エラストマー社製)3部および安定剤として
ブチル錫系安定剤2部、安定化助剤として合成ゼオライ
トを0.5部、滑剤を2部、充填剤として二酸化チタン
4.5部を加えた。この配合物のハンドブレンドをおこ
ない均一な配合物を得た。
Comparative Example 1 A vinyl chloride resin having a polymerization degree of 1000 was post-chlorinated to obtain a chlorinated vinyl chloride resin having a chlorination degree of 67%. 100 parts of this chlorinated vinyl chloride resin
6 parts of B22 (MBS manufactured by Kanegafuchi Chemical Co., Ltd.) having a butadiene content of 46% as a shock absorber and a chlorine content of 36
% Chlorinated polyethylene Tyrin 3615P (manufactured by Dupont Dow Elastomers), 3 parts of a butyltin-based stabilizer as a stabilizer, 0.5 part of a synthetic zeolite as a stabilizing aid, 2 parts of a lubricant, and titanium dioxide as a filler. 4.5 parts were added. The blend was hand blended to obtain a uniform blend.

【0015】このブレンド配合物を、200℃の8イン
チのロールにて3分間混練し、205℃のプレス機にて
10分間プレス後に切削して試験片を得た。JIS K
7110に準じて−7℃でのアイゾット衝撃試験をお
こなったところアイゾット衝撃試験値は8.5kg・c
m/cm2であった。また、JIS K 7113に準
じて82℃での引張試験をおこなったところ、引張強度
は241kg/cm2であった。また、JIS K 7
206に準じた5kg荷重でのVicat軟化点は11
6.2℃だった。
This blend was kneaded with an 8-inch roll at 200 ° C. for 3 minutes, pressed with a press machine at 205 ° C. for 10 minutes, and then cut to obtain a test piece. JIS K
When an Izod impact test at -7 ° C was performed according to 7110, the Izod impact test value was 8.5 kg · c.
m / cm 2 . In addition, when a tensile test was conducted at 82 ° C. according to JIS K7113, the tensile strength was 241 kg / cm 2 . In addition, JIS K7
The Vicat softening point at 5 kg load according to 206 is 11
6.2 ° C.

【0016】上記の実施例および比較例の結果を表1に
まとめた。
Table 1 summarizes the results of the above Examples and Comparative Examples.

【0017】[0017]

【表1】 [Table 1]

【0018】[0018]

【発明の効果】ポリオルガノシロキサン2〜8重量部お
よびアクリル系モディファイヤー樹脂1〜5重量部を含
んでなる塩素化塩化ビニル系樹脂組成物を用いると、成
形体の高温での引張強度を維持したままで低温での耐衝
撃強度を向上でき、また耐熱性も向上できる。
When a chlorinated vinyl chloride resin composition comprising 2 to 8 parts by weight of a polyorganosiloxane and 1 to 5 parts by weight of an acrylic modifier resin is used, the tensile strength of a molded article at a high temperature is maintained. The impact strength at low temperatures can be improved as it is, and the heat resistance can be improved.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 塩素化前の重合度が600〜1500で
あり、塩素化度が62〜70重量%である塩素化塩化ビ
ニル系樹脂100重量部とポリオルガノシロキサン2〜
8重量部およびアクリル系モディファイヤー樹脂1〜7
重量部を含んでなる塩素化塩化ビニル系樹脂組成物。
1. A chlorinated vinyl chloride resin having a degree of polymerization of 600 to 1500 before chlorination and a chlorination degree of 62 to 70% by weight, and 100 parts by weight of polyorganosiloxane 2
8 parts by weight and acrylic modifier resin 1 to 7
A chlorinated vinyl chloride resin composition comprising parts by weight.
JP2000047895A 2000-02-24 2000-02-24 Chlorinated vinyl chloride-based resin composition Pending JP2001234017A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2000047895A JP2001234017A (en) 2000-02-24 2000-02-24 Chlorinated vinyl chloride-based resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2000047895A JP2001234017A (en) 2000-02-24 2000-02-24 Chlorinated vinyl chloride-based resin composition

Publications (1)

Publication Number Publication Date
JP2001234017A true JP2001234017A (en) 2001-08-28

Family

ID=18570067

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002284947A (en) * 2001-03-26 2002-10-03 Sekisui Chem Co Ltd Vinyl chloride-based resin composition
JP2002284950A (en) * 2001-03-26 2002-10-03 Sekisui Chem Co Ltd Vinyl chloride-base resin composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002284947A (en) * 2001-03-26 2002-10-03 Sekisui Chem Co Ltd Vinyl chloride-based resin composition
JP2002284950A (en) * 2001-03-26 2002-10-03 Sekisui Chem Co Ltd Vinyl chloride-base resin composition
JP4555494B2 (en) * 2001-03-26 2010-09-29 積水化学工業株式会社 Vinyl chloride resin composition

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