JPH11181206A - Chlorinated vinyl chloride-based resin composition - Google Patents

Chlorinated vinyl chloride-based resin composition

Info

Publication number
JPH11181206A
JPH11181206A JP9356873A JP35687397A JPH11181206A JP H11181206 A JPH11181206 A JP H11181206A JP 9356873 A JP9356873 A JP 9356873A JP 35687397 A JP35687397 A JP 35687397A JP H11181206 A JPH11181206 A JP H11181206A
Authority
JP
Japan
Prior art keywords
vinyl chloride
parts
chlorinated
weight
chloride resin
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
JP9356873A
Other languages
Japanese (ja)
Inventor
Toshio Okuhara
登志夫 奥原
Tsuyoshi Suzuki
毅之 鈴木
Minoru Isshiki
實 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 JP9356873A priority Critical patent/JPH11181206A/en
Publication of JPH11181206A publication Critical patent/JPH11181206A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain a chlorinated vinyl chloride-based resin composition excellent in heat stability and at the same time, capable of increasing the extrusion volume in extrusion molding, resulting in its high productivity, therefore, suitable for extrusion pipe molding. SOLUTION: This composition is obtained by including 100 pts.wt. of a resin component comprising 80-99 pts.wt. of a chlorinated vinyl chloride-based resin having a polymerization degree of 600-1500 before chlorination and a chlorination degree of 62-70 wt.%, and 1-20 pts.wt. of a vinyl chloride-based paste resin produced by emulsion polymerization or minute suspension polymerization and having a particle size of 5-100 μm after spray drying and having a polymerization degree of 600-2,100, and 3-15 pts.wt. of an impact modifier.

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】この発明は、塩素化塩化ビニ
ル系樹脂組成物に関する。
[0001] The present invention relates to a chlorinated vinyl chloride resin composition.

【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長を有し、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。また、成形に際しては、塩
素化塩化ビニル系樹脂は、汎用の塩化ビニル系樹脂用押
出成形機によって成形でき、このことが塩素化塩化ビニ
ル系樹脂を広く使用しやすくする要因になっている。
2. Description of the Related Art A molded article of 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 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. In molding, the chlorinated vinyl chloride-based resin can be molded by a general-purpose vinyl chloride-based resin extrusion molding machine, which is a factor that makes the chlorinated vinyl chloride-based resin widely usable.

【0003】一方、塩素化塩化ビニル系樹脂を成形する
にあたって、塩素化塩化ビニル系樹脂は塩化ビニル系樹
脂に比べて熱安定性が劣り、成形加工中に焼けやすいと
いう欠点を持っている。例えば、塩素化塩化ビニル系樹
脂を熱水用パイプに押出成形する際、着色がおこった
り、場合によっては押出成形中に焼けが生じ、商品とし
て使えない等の問題を生ずることがあった。更に、塩素
化塩化ビニル系樹脂を熱水用パイプに押出成形すると、
押出成形機のダイ圧力および押出トルクが上昇して焼け
る。これを防止するために、通常の塩化ビニル系樹脂用
の押出成形機では、塩化ビニル系樹脂に比べて塩素化塩
化ビニル系樹脂のフィード量を抑えて吐出量を低下させ
てダイ圧力および押出トルクを抑える必要がある。すな
わち、塩素化塩化ビニル系樹脂のパイプ用押出成形にあ
たっては吐出量が少なく、生産性が悪いという問題があ
る。
[0003] On the other hand, when molding a chlorinated vinyl chloride resin, the chlorinated vinyl chloride resin is inferior in thermal stability to the vinyl chloride resin and has a drawback that it is easily burned during molding. For example, when extruding a chlorinated vinyl chloride resin into a hot water pipe, coloring may occur, and in some cases, burning may occur during the extrusion molding, which may cause problems such as being unusable as a product. Furthermore, when chlorinated vinyl chloride resin is extruded into a hot water pipe,
The die pressure and extrusion torque of the extruder rise and burn. In order to prevent this, in a typical extruder for vinyl chloride resin, the feed rate of the chlorinated vinyl chloride resin is reduced compared to the vinyl chloride resin, the discharge rate is reduced, and the die pressure and extrusion torque are reduced. Need to be suppressed. That is, when extruding a chlorinated vinyl chloride resin for a pipe, there is a problem that the discharge amount is small and productivity is poor.

【0004】[0004]

【発明が解決しようとする課題】本発明の目的は、熱安
定性に優れると同時に、押出成形時に吐出量を多くで
き、生産性を高くできる、押出パイプ成形用として好ま
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 It is an object of the present invention to provide a chlorinated vinyl chloride resin which is excellent in thermal stability, can increase the discharge rate at the time of extrusion molding and can increase productivity, and is preferable for extrusion pipe molding. It is to provide a composition.

【0005】[0005]

【課題を解決するための手段】本発明によれば、上記の
目的は、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80〜99重量部、乳化重合または微細懸濁重合で
製造された、噴霧乾燥後の粒子径が5〜100μmであ
り、重合度が600〜2100である塩化ビニル系ペー
スト樹脂1〜20重量部を含む樹脂成分100重量部、
並びに衝撃吸収剤を3〜15重量部、および所望により
安定剤ならびに滑剤を含んでなる塩素化塩化ビニル系樹
脂組成物により達成される。
According to the present invention, an object of the present invention is to provide a polymerizable composition having a polymerization degree before chlorination of 600 to 1500,
80 to 99 parts by weight of a chlorinated vinyl chloride resin having a chlorination degree of 62 to 70% by weight, a particle diameter after spray drying produced by emulsion polymerization or fine suspension polymerization of 5 to 100 μm, 100 parts by weight of a resin component containing 1 to 20 parts by weight of a vinyl chloride paste resin having a
And a chlorinated vinyl chloride-based resin composition containing 3 to 15 parts by weight of a shock absorber and, if desired, a stabilizer and a lubricant.

【0006】本発明の樹脂組成物では、塩素化塩化ビニ
ル系樹脂80重量部以上に対して、塩化ビニル系ペース
ト樹脂の量を20重量部以下にする必要がある。塩素化
塩化ビニル系樹脂に対する塩化ビニル系ペースト樹脂の
割合がこれ以上になると、得られる塩素化塩化ビニル系
樹脂組成物からの成形品、例えばパイプの耐熱性が低下
し、初期の耐熱性が高いという本発明の利点が失われ
る。
In the resin composition of the present invention, the amount of the vinyl chloride paste resin must be 20 parts by weight or less based on 80 parts by weight or more of the chlorinated vinyl chloride resin. When the ratio of the vinyl chloride-based paste resin to the chlorinated vinyl chloride-based resin is more than this, the heat resistance of the molded article from the obtained chlorinated vinyl chloride-based resin composition, for example, the pipe is reduced, and the initial heat resistance is high. The advantage of the present invention is lost.

【0007】本発明においては、塩素化塩化ビニル系パ
イプ用樹脂として、塩素化前の重合度が600〜150
0で、塩素化度が62〜70重量%である塩素化塩化ビ
ニル系樹脂を使用する。「塩化ビニル系樹脂」は、塩化
ビニルホモポリマーのみならず、塩化ビニルと20重量
%以下の他のモノマー(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、ビニルエステル等)少なくと
も1種とのコポリマーを包含する。
In the present invention, the chlorinated vinyl chloride pipe resin has a polymerization degree before chlorination of 600 to 150.
0, a chlorinated vinyl chloride resin having a chlorination degree of 62 to 70% by weight is used. “Vinyl chloride resin” includes not only vinyl chloride homopolymer but also vinyl chloride and other monomers of 20% by weight or less (eg, ethylene, propylene, vinyl acetate, allyl chloride, allyl glycidyl ether, acrylate, vinyl ester) Etc.) copolymers with at least one.

【0008】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成形品が得られず、
また塩素化度が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。
If the 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 1,500, the resin composition It is not preferable because the processing is not easy. If the chlorination degree of the chlorinated vinyl chloride resin is less than 62% by weight, a molded article having sufficient heat resistance cannot be obtained,
On the other hand, if the chlorination degree exceeds 70% by weight, the melt viscosity increases, and the processing of the resin composition involves technical difficulties.

【0009】本発明の樹脂組成物では、塩化ビニル系ペ
ースト樹脂として、乳化重合または微細懸濁重合で製造
された、噴霧乾燥後の粒子径が5〜100μm、重合度
が600〜2100の塩化ビニル系ペースト樹脂を用い
る。本発明の目的を達成するために、塩化ビニル系ペー
スト樹脂は、乳化剤を用いた乳化重合または微細懸濁重
合で製造する必要がある。この理由は不明であるが、お
そらく塩化ビニル系ペースト樹脂表面に残存した乳化剤
が本発明の効果を達成するのに寄与しているものと思わ
れる。
In the resin composition of the present invention, a vinyl chloride paste resin having a particle size after spray drying of 5 to 100 μm and a polymerization degree of 600 to 2100, produced by emulsion polymerization or fine suspension polymerization, is used. A system paste resin is used. In order to achieve the object of the present invention, the vinyl chloride paste resin needs to be produced by emulsion polymerization using an emulsifier or fine suspension polymerization. Although the reason is unknown, it is considered that the emulsifier remaining on the surface of the vinyl chloride-based paste resin contributes to achieving the effects of the present invention.

【0010】乳化重合または微細懸濁重合で製造された
塩化ビニル系ペースト樹脂の噴霧乾燥後の粒子径は、通
常5〜100μm、好ましくは10〜50μm、かつ重合
度は600〜2100、好ましくは800〜1600で
ある。塩化ビニル系ペースト樹脂の噴霧乾燥後の粒子径
が5μmより小さいと、組成物のブレンド時に細かいペ
ースト樹脂のまい上がりが多くなり、作業環境上良くな
い。また、粒子径が100μmを越えると、本発明の効
果である押出成形時の吐出量を上げる効果がそれほど見
られなくなる。重合度が600未満であると、十分な機
械的強度が得られず、一方、その重合度が2100を超
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。
The particle size of the vinyl chloride paste resin produced by emulsion polymerization or fine suspension polymerization after spray drying is usually 5 to 100 μm, preferably 10 to 50 μm, and the degree of polymerization is 600 to 2100, preferably 800. 11600. If the particle size of the vinyl chloride-based paste resin after spray drying is smaller than 5 μm, fine paste resin tends to be swelled when the composition is blended, which is not good for the working environment. On the other hand, if the particle diameter exceeds 100 μm, the effect of the present invention, that is, the effect of increasing the discharge amount at the time of extrusion molding, cannot be seen so much. If the degree of polymerization is less than 600, sufficient mechanical strength cannot be obtained, while if the degree of polymerization exceeds 2100, processing of the resin composition is not easy, which is not preferable.

【0011】本発明では、塩素化塩化ビニル系樹脂を8
0重量部以上と塩化ビニル系ペースト樹脂を20重量部
以下に対して、衝撃吸収剤3〜15重量部を配合する。
衝撃吸収剤としては、メチルメタクリレート−ブダジエ
ン−スチレン共重合体(MBS)、ABS、MABS、
CPE、アクリルゴムを主成分とした衝撃吸収剤など、
通常に塩素化塩化ビニル系樹脂の衝撃吸収剤として使用
されているものが使用できる。特に、耐衝撃性と耐熱性
のバランスを持たせるために、衝撃吸収剤として、MB
Sと塩素化ポリエチレンとの混合物、またはMBSのみ
を用いることが好ましく、その場合、衝撃吸収剤の合計
含有量は、塩素化塩化ビニル系樹脂80重量部以上と塩
化ビニル系ペースト樹脂を20重量部以下の樹脂成分1
00重量部に対して、3〜15重量部とするのが望まし
い。
In the present invention, the chlorinated vinyl chloride resin is
The shock absorber is mixed in an amount of 3 to 15 parts by weight with respect to 0 parts by weight or more and 20 parts by weight or less of the vinyl chloride paste resin.
Examples of the shock absorber include methyl methacrylate-butadiene-styrene copolymer (MBS), ABS, MABS,
CPE, shock absorbers based on acrylic rubber, etc.
What is usually used as a shock absorber of a chlorinated vinyl chloride resin can be used. In particular, MB is used as a shock absorber to provide a balance between impact resistance and heat resistance.
It is preferable to use a mixture of S and chlorinated polyethylene or only MBS. In that case, the total content of the shock absorber is 80 parts by weight or more of chlorinated vinyl chloride resin and 20 parts by weight of vinyl chloride paste resin. The following resin component 1
Desirably, the amount is 3 to 15 parts by weight with respect to 00 parts by weight.

【0012】配合する衝撃吸収剤の量が3重量部未満で
あると、成型品、特にパイプの耐衝撃物性が低下し、1
5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。成型品、例えばパイプの耐衝
撃物性および耐熱性のバランスから、衝撃吸収剤とし
て、MBS4〜12重量部と、塩素含有量が10〜50
重量%の塩素化ポリエチレン1〜5重量部との混合物、
またはMBSのみを使用することが好ましい。また、耐
衝撃剤がMBSおよび塩素化ポリエチレンの混合物であ
るときは、塩素化ポリエチレン中の塩素含有量が40〜
50重量%であることが、耐衝撃物性の発現の点で更に
好ましい。
If the amount of the shock absorbing agent to be blended is less than 3 parts by weight, the impact resistance of a molded product, especially a pipe, is lowered, and
If the amount exceeds 5 parts by weight, the heat resistance, which is a characteristic of the chlorinated vinyl chloride resin, is reduced. From the balance of impact resistance and heat resistance of a molded product, for example, a pipe, MBS 4 to 12 parts by weight and a chlorine content of 10 to 50 are used as a shock absorber.
A mixture with 1 to 5 parts by weight of chlorinated polyethylene by weight
Alternatively, it is preferable to use only MBS. When the impact modifier is a mixture of MBS and chlorinated polyethylene, the chlorine content in the chlorinated polyethylene is 40 to 40%.
It is more preferable that the content be 50% by weight in view of the development of impact resistance.

【0013】本発明では、塩素化塩化ビニル系樹脂に、
上記の塩化ビニル系ペースト樹脂と衝撃吸収剤の他に、
所望により安定剤と滑剤を配合する。安定剤および滑剤
は、塩素化塩化ビニル系樹脂の成形加工において通常用
いられるものであってよく、とくに錫系安定剤が好まし
い。このような安定剤として、アルキル錫化合物(例え
ばメチル錫、ブチル錫、オクチル錫、混合金属アルキル
錫)が挙げられる。その他、メチル錫メルカプト、オク
チル錫メルカプト、ブチル錫メルカプト、ジアルキル錫
ビス(アルキルメルカプトカルボン酸塩)、オクチル錫マ
レエート、ブチル錫マレエート、オクチル錫ラウレー
ト、ブチル錫ラウレート、ブチル錫ラウレートマレエー
ト、オクチル錫カルボキシレート、ブチル錫カルボキシ
レート等のエステルが用いられる。
In the present invention, the chlorinated vinyl chloride resin is
In addition to the above vinyl chloride paste resin and shock absorber,
If necessary, a stabilizer and a lubricant are blended. The stabilizer and the lubricant may be those usually used in molding of chlorinated vinyl chloride resin, and a tin stabilizer is particularly preferable. Such stabilizers include alkyl tin compounds (eg, methyl tin, butyl tin, octyl tin, mixed metal alkyl tins). In addition, methyltin mercapto, octyltin mercapto, butyltin mercapto, dialkyltin bis (alkylmercaptocarboxylate), octyltin maleate, butyltin maleate, octyltin laurate, butyltin laurate, butyltin laurate maleate, octyltin Esters such as carboxylate and butyltin carboxylate are used.

【0014】安定剤の配合量は、塩素化塩化ビニル系樹
脂80重量部以上と塩化ビニル系ペースト樹脂20重量
部以下の樹脂成分100重量部に対して、1.5〜5重
量部であることが好ましい。安定剤が1.5重量部未満
では、塩素化塩化ビニル系樹脂の熱安定性が低下するの
で好ましくない。また、安定剤が5重量部が越えると、
熱安定性の効果は頭打ちの状態となり、添加量に見合っ
た熱安定性が得られなくなる。
The compounding amount of the stabilizer is 1.5 to 5 parts by weight based on 100 parts by weight of the resin component containing 80 parts by weight or more of the chlorinated vinyl chloride resin and 20 parts by weight or less of the vinyl chloride paste resin. Is preferred. If the amount of the stabilizer is less than 1.5 parts by weight, the thermal stability of the chlorinated vinyl chloride resin is undesirably reduced. When the amount of the stabilizer exceeds 5 parts by weight,
The effect of thermal stability reaches a plateau, and thermal stability corresponding to the added amount cannot be obtained.

【0015】滑剤としては、ジ及びトリオレエートのポ
リグリセロール、ポリエチレン、酸化ポリエチレン、高
分子量パラフィンワックスが挙げられる。好ましい滑剤
は、ポリエチレンワックスである。滑剤の配合量は、塩
素化塩化ビニル系樹脂と塩化ビニル系ペースト樹脂とを
含む樹脂成分100重量部に対して、1.5〜4重量部
であるのが好ましい。滑剤が1.5重量部未満であれ
ば,溶融粘度が高くなるため、押出加工性が悪くなる。
また、滑剤が4重量部を越えると、樹脂と金属との滑性
が強くなりすぎ、押出加工時の樹脂吐出に脈動を生じる
ことがあるので、好ましくない。
[0015] Lubricants include di- and trioleate polyglycerol, polyethylene, polyethylene oxide, high molecular weight paraffin wax. A preferred lubricant is polyethylene wax. The amount of the lubricant is preferably 1.5 to 4 parts by weight based on 100 parts by weight of the resin component containing the chlorinated vinyl chloride resin and the vinyl chloride paste resin. If the amount of the lubricant is less than 1.5 parts by weight, the melt viscosity will be high, and the extrudability will be poor.
On the other hand, if the amount of the lubricant exceeds 4 parts by weight, the lubricity between the resin and the metal becomes too strong, and pulsation may occur in the resin discharge during extrusion, which is not preferable.

【0016】本発明の塩素化塩化ビニル系樹脂組成物に
は、上記添加物の他に、通常塩素化塩化ビニル系樹脂に
配合される他の添加剤、例えば二酸化チタンや炭酸カル
シウムなどの充填剤を配合してよい。また、着色剤とし
て、塩素化塩化ビニル系樹脂の成形加工において通常用
いられるものを使用してよい。
In the chlorinated vinyl chloride resin composition of the present invention, in addition to the above-mentioned additives, other additives usually added to the chlorinated vinyl chloride resin, for example, fillers such as titanium dioxide and calcium carbonate. May be blended. In addition, as the coloring agent, a coloring agent that is usually used in molding of a chlorinated vinyl chloride resin may be used.

【0017】[0017]

【実施例】以下に実施例と比較例を挙げて本発明を説明
する。言うまでもなく、本発明は以下の実施例のみに限
定されるわけではない。尚、実施例および比較例中
「部」または「%」は、特に記載のない限り「重量部」
または「重量%」を意味する。
The present invention will be described below with reference to examples and comparative examples. Needless to say, the present invention is not limited to only the following examples. In the Examples and Comparative Examples, “parts” or “%” means “parts by weight” unless otherwise specified.
Or "wt%".

【0018】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(CPVC)を得
た。この塩素化塩化ビニル樹脂95部に、重合度が14
00で噴霧乾燥後の粒子径が37μmである、乳化重合
で得た塩化ビニル系ペースト樹脂(ペースト樹脂
(1))5部、MBS(鐘淵化学工業社製B561)6
部、および塩素含有量35%の塩素化ポリエチレン(C
PE)3部を加え、更に安定剤としてオクチル錫メルカ
プト2部、滑剤としてポリエチレンワックス2部、およ
び充填剤として二酸化チタン5部を加え、混合物のブレ
ンドを行って、均一な配合物を得た。
Example 1 A vinyl chloride resin having a degree of polymerization of 1000 was post-chlorinated to obtain a chlorinated vinyl chloride resin (CPVC) having a degree of chlorination of 67%. 95 parts of this chlorinated vinyl chloride resin has a degree of polymerization of 14
5 parts of a vinyl chloride paste resin (paste resin (1)) obtained by emulsion polymerization and having a particle diameter of 37 μm after spray-drying at 00, MBS (B561 manufactured by Kanegafuchi Chemical Co., Ltd.) 6
Parts and a chlorinated polyethylene having a chlorine content of 35% (C
PE), 2 parts of octyltin mercapto as a stabilizer, 2 parts of polyethylene wax as a lubricant, and 5 parts of titanium dioxide as a filler were blended to obtain a uniform mixture.

【0019】このブレンド配合物をロール温度200℃
にて3分間混練し、更に得られたロールシートを温度2
00℃にて10分間プレスし、以下の物性試験に供し
た。JIS−K−7111に準じてシャルピー衝撃試験
を23℃および0℃で行ったところ、23℃および0℃
でのシャルピー衝撃試験値は、それぞれ23.6kg・cm
/cm2および16.0kg・cm/cm2であった。流動特性を
評価するために、長さ10mmおよび直径1mmの細管中
を、300kgの荷重下、200℃で流れるロールシート
の量を測定した(B法フロー試験)。毎秒2.4×10
-2ccの流量が得られ、流動特性が良好であることがわか
った。
The blended composition was rolled at a temperature of 200 ° C.
And kneaded for 3 minutes at a temperature of 2 ° C.
It was pressed at 00 ° C. for 10 minutes and subjected to the following physical property tests. When the Charpy impact test was performed at 23 ° C. and 0 ° C. according to JIS-K-7111, the results were 23 ° C. and 0 ° C.
Impact test values of 23.6 kg · cm
/ Cm 2 and 16.0 kg · cm / cm 2 . In order to evaluate the flow characteristics, the amount of the roll sheet flowing at 200 ° C. under a load of 300 kg in a thin tube having a length of 10 mm and a diameter of 1 mm was measured (Method B flow test). 2.4 × 10 per second
A flow rate of -2 cc was obtained and the flow characteristics were found to be good.

【0020】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90部に、重合度が1400で噴霧乾燥
後の粒子径が37μmである、乳化重合で得た塩化ビニ
ル系ペースト樹脂10部、MBS(鐘淵化学工業社製B
561)6部、および塩素含有量35%の塩素化ポリエ
チレン3部を加え、更に安定剤としてオクチル錫メルカ
プト2部、滑剤としてポリエチレンワックス2部、およ
び充填剤として二酸化チタン5部を加え、混合物のブレ
ンドを行って、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%. To 90 parts of this chlorinated vinyl chloride resin, 10 parts of a vinyl chloride paste resin obtained by emulsion polymerization having a degree of polymerization of 1400 and a particle diameter of 37 μm after spray drying, MBS (Baneka Chemical Industry Co., Ltd.)
561) 6 parts, and 3 parts of chlorinated polyethylene having a chlorine content of 35%, 3 parts of octyltin mercapto as a stabilizer, 2 parts of polyethylene wax as a lubricant, and 5 parts of titanium dioxide as a filler are added. Blending was performed to obtain a uniform formulation.

【0021】このブレンド配合物をロール温度200℃
にて3分間混練し、更に得られたロールシートを温度2
00℃にて10分間プレスし、以下の物性試験に供し
た。実施例1と同様にシャルピー衝撃試験を行ったとこ
ろ、23℃および0℃でのシャルピー衝撃試験値は、そ
れぞれ24.9kg・cm/cm2および16.2kg・cm/cm2
であった。実施例1と同様にB法フロー試験を行ったと
ころ、毎秒2.5×10-2ccの流量が得られ、流動特性
が良好であることがわかった。
The blend formulation is rolled at a temperature of 200 ° C.
And kneaded for 3 minutes at a temperature of 2 ° C.
It was pressed at 00 ° C. for 10 minutes and subjected to the following physical property tests. Was subjected to a Charpy impact test in the same manner as in Example 1, the Charpy impact test value at 23 ° C. and 0 ℃, respectively 24.9kg · cm / cm 2 and 16.2kg · cm / cm 2
Met. A flow test of method B was performed in the same manner as in Example 1. As a result, a flow rate of 2.5 × 10 −2 cc / sec was obtained, and it was found that the flow characteristics were good.

【0022】実施例3 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90部に、重合度が800で噴霧乾燥後
の粒子径が35μmである、乳化重合で得た塩化ビニル
系ペースト樹脂(ペースト樹脂(2))10部、MBS
(鐘淵化学工業社製B561)6部、および塩素含有量
35%の塩素化ポリエチレン3部を加え、更に安定剤と
してオクチル錫メルカプト2部、滑剤としてポリエチレ
ンワックス2部、および充填剤として二酸化チタン5部
を加えた。この混合物のブレンドを行って、均一な配合
物を得た。
Example 3 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%. 90 parts of the chlorinated vinyl chloride resin, 10 parts of a vinyl chloride paste resin (paste resin (2)) obtained by emulsion polymerization, having a degree of polymerization of 800 and a particle diameter of 35 μm after spray drying, MBS
(B561 manufactured by Kanegafuchi Chemical Co., Ltd.), 6 parts of chlorinated polyethylene having a chlorine content of 35%, 3 parts of octyltin mercapto as a stabilizer, 2 parts of polyethylene wax as a lubricant, and titanium dioxide as a filler. 5 parts were added. This mixture was blended to obtain a uniform blend.

【0023】このブレンド配合物をロール温度200℃
にて3分間混練し、更に得られたロールシートを温度2
00℃にて10分間プレスし、以下の物性試験に供し
た。実施例1と同様にシャルピー衝撃試験を行ったとこ
ろ、23℃および0℃でのシャルピー衝撃試験値は、そ
れぞれ22.6kg・cm/cm2および17.0kg・cm/cm2
であった。実施例1と同様にB法フロー試験を行ったと
ころ、毎秒2.1×10-2ccの流量が得られ、流動特性
が良好であることがわかった。
The blend formulation is rolled at a temperature of 200 ° C.
And kneaded for 3 minutes at a temperature of 2 ° C.
It was pressed at 00 ° C. for 10 minutes and subjected to the following physical property tests. Was subjected to a Charpy impact test in the same manner as in Example 1, the Charpy impact test value at 23 ° C. and 0 ℃, respectively 22.6kg · cm / cm 2 and 17.0kg · cm / cm 2
Met. A flow test of Method B was performed in the same manner as in Example 1. As a result, a flow rate of 2.1 × 10 -2 cc / sec was obtained, and it was found that the flow characteristics were good.

【0024】実施例4 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95部に、重合度が1400で噴霧乾燥
後の粒子径が37μmである、乳化重合で得た塩化ビニ
ル系ペースト樹脂5部、MBS(鐘淵化学工業社製B2
2)8部および塩素含有量35%の塩素化ポリエチレン
3部を加え、更に安定剤としてオクチル錫メルカプト2
部、滑剤としてポリエチレンワックス2部、および充填
剤として二酸化チタン5部を加えた。この混合物のブレ
ンドを行って、均一な配合物を得た。
Example 4 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%. To 95 parts of this chlorinated vinyl chloride resin, 5 parts of a vinyl chloride paste resin obtained by emulsion polymerization having a degree of polymerization of 1400 and a particle diameter of 37 μm after spray drying, MBS (B2 manufactured by Kaneguchi Chemical Co., Ltd.)
2) 8 parts and 3 parts of chlorinated polyethylene having a chlorine content of 35% were added, and octyltin mercapto 2 was further used as a stabilizer.
Parts, 2 parts of polyethylene wax as a lubricant and 5 parts of titanium dioxide as a filler. This mixture was blended to obtain a uniform blend.

【0025】このブレンド配合物をロール温度200℃
にて3分間混練し、更に得られたロールシートを温度2
00℃にて10分間プレスし、以下の物性試験に供し
た。実施例1と同様にシャルピー衝撃試験を行ったとこ
ろ、23℃および0℃でのシャルピー衝撃試験値は、そ
れぞれ24.9kg・cm/cm2および17.0kg・cm/cm2
であった。実施例1と同様にB法フロー試験を行ったと
ころ、毎秒2.1×10-2ccの流量が得られ、流動特性
が良好であることがわかった。
[0025] The blend formulation is rolled at a temperature of 200 ° C.
And kneaded for 3 minutes at a temperature of 2 ° C.
It was pressed at 00 ° C. for 10 minutes and subjected to the following physical property tests. Was subjected to a Charpy impact test in the same manner as in Example 1, the Charpy impact test value at 23 ° C. and 0 ℃, respectively 24.9kg · cm / cm 2 and 17.0kg · cm / cm 2
Met. A flow test of Method B was performed in the same manner as in Example 1. As a result, a flow rate of 2.1 × 10 -2 cc / sec was obtained, and it was found that the flow characteristics were good.

【0026】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、MBS(鐘淵化学工業社製
B561)6部および塩素含有量35%の塩素化ポリエ
チレン3部を加え、更に安定剤としてオクチル錫メルカ
プト2部、滑剤としてポリエチレンワックス2部、およ
び充填剤として二酸化チタン5部を加えた。この混合物
のブレンドを行って、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%. To 100 parts of the chlorinated vinyl chloride resin, 6 parts of MBS (B561 manufactured by Kanegafuchi Chemical Co., Ltd.) and 3 parts of chlorinated polyethylene having a chlorine content of 35% were added, and 2 parts of octyltin mercapto was used as a stabilizer, and polyethylene was used as a lubricant. 2 parts of wax and 5 parts of titanium dioxide as filler were added. This mixture was blended to obtain a uniform blend.

【0027】このブレンド配合物をロール温度200℃
にて3分間混練し、更に得られたロールシートを温度2
00℃にて10分間プレスし、以下の物性試験に供し
た。実施例1と同様にシャルピー衝撃試験を行ったとこ
ろ、23℃および0℃でのシャルピー衝撃試験値は、そ
れぞれ22.7kg・cm/cm2および14.8kg・cm/cm2
であった。実施例1と同様にB法フロー試験を行ったと
ころ、毎秒1.7×10-2ccの流量が得られ、流動特性
はあまりよくなかった。
The blend was rolled at a temperature of 200 ° C.
And kneaded for 3 minutes at a temperature of 2 ° C.
It was pressed at 00 ° C. for 10 minutes and subjected to the following physical property tests. When the Charpy impact test was conducted in the same manner as in Example 1, the Charpy impact test values at 23 ° C. and 0 ° C. were 22.7 kg · cm / cm 2 and 14.8 kg · cm / cm 2, respectively.
Met. When the method B flow test was performed in the same manner as in Example 1, a flow rate of 1.7 × 10 −2 cc / sec was obtained, and the flow characteristics were not so good.

【0028】比較例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、MBS(鐘淵化学工業社製
B22)8部および塩素含有量35%の塩素化ポリエチ
レン3部を加え、更に安定剤としてオクチル錫メルカプ
ト2部、滑剤としてポリエチレンワックス2部、および
充填剤として二酸化チタン5部を加えた。この混合物の
ブレンドを行って、均一な配合物を得た。
Comparative 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%. To 100 parts of this chlorinated vinyl chloride resin, 8 parts of MBS (B22 manufactured by Kaneka Chemical Industry Co., Ltd.) and 3 parts of chlorinated polyethylene having a chlorine content of 35% were added, 2 parts of octyltin mercapto was used as a stabilizer, and polyethylene was used as a lubricant. 2 parts of wax and 5 parts of titanium dioxide as filler were added. This mixture was blended to obtain a uniform blend.

【0029】このブレンド配合物をロール温度200℃
にて3分間混練し、更に得られたロールシートを温度2
00℃にて10分間プレスし、以下の物性試験に供し
た。実施例1と同様にシャルピー衝撃試験を行ったとこ
ろ、23℃および0℃でのシャルピー衝撃試験値は、そ
れぞれ24.1kg・cm/cm2および16.4kg・cm/cm2
であった。実施例1と同様にB法フロー試験を行ったと
ころ、毎秒1.5×10-2ccの流量が得られ、流動特性
はあまりよくなかった。
The blend was rolled at 200 ° C.
And kneaded for 3 minutes at a temperature of 2 ° C.
It was pressed at 00 ° C. for 10 minutes and subjected to the following physical property tests. Was subjected to a Charpy impact test in the same manner as in Example 1, the Charpy impact test value at 23 ° C. and 0 ℃, respectively 24.1kg · cm / cm 2 and 16.4kg · cm / cm 2
Met. When the method B flow test was performed in the same manner as in Example 1, a flow rate of 1.5 × 10 −2 cc / sec was obtained, and the flow characteristics were not so good.

【0030】比較例3 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90部に、重合度が1000で粒子径が
1300μmである、懸濁重合で得た塩化ビニル樹脂
(PVC)10部、MBS(鐘淵化学工業社製B56
1)6部および塩素含有量35%の塩素化ポリエチレン
3部を加え、更に安定剤としてオクチル錫メルカプト2
部、滑剤としてポリエチレンワックス2部、および充填
剤として二酸化チタン5部を加えた。この混合物のブレ
ンドを行って、均一な配合物を得た。
Comparative Example 3 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%. To 90 parts of this chlorinated vinyl chloride resin, 10 parts of a vinyl chloride resin (PVC) obtained by suspension polymerization having a degree of polymerization of 1000 and a particle size of 1300 μm, and MBS (Kanebuchi Chemical Industries B56)
1) 6 parts and 3 parts of chlorinated polyethylene having a chlorine content of 35% were added, and octyltin mercapto 2 was further used as a stabilizer.
Parts, 2 parts of polyethylene wax as a lubricant and 5 parts of titanium dioxide as a filler. This mixture was blended to obtain a uniform blend.

【0031】このブレンド配合物をロール温度200℃
にて3分間混練し、更に得られたロールシートを温度2
00℃にて10分間プレスし、物性試験に供した。実施
例1と同様にシャルピー衝撃試験を行ったところ、23
℃および0℃でのシャルピー衝撃試験値は、それぞれ2
3.6kg・cm/cm2および16.8kg・cm/cm2であっ
た。実施例1と同様にB法フロー試験を行ったところ、
毎秒1.8×10-2ccの流量が得られ、流動特性はあま
りよくなかった。
The blend composition is rolled at a temperature of 200 ° C.
And kneaded for 3 minutes at a temperature of 2 ° C.
It pressed at 00 degreeC for 10 minutes, and was subjected to the physical property test. When a Charpy impact test was performed in the same manner as in Example 1, the result was 23.
The Charpy impact test values at 0 ° C and 0 ° C were 2
It was 3.6 kg · cm / cm 2 and 16.8 kg · cm / cm 2 . When a method B flow test was performed in the same manner as in Example 1,
A flow rate of 1.8 × 10 -2 cc per second was obtained and the flow characteristics were not very good.

【0032】実施例5 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95部に、重合度が1400で噴霧乾燥
後の粒子径が37μmである、乳化重合で得た塩化ビニ
ル系ペースト樹脂5部、MBS(鐘淵化学工業社製B5
61)6部、および塩素含有量35%の塩素化ポリエチ
レン3部を加え、更に安定剤としてオクチル錫メルカプ
ト3部、滑剤としてポリエチレンワックス2部、充填剤
として二酸化チタンを5部、および黄色着色剤0.00
8部を加えた。この混合物を、300リットルのスーパ
ーミキサーにて130℃まで昇温してブレンドして、均
一な配合物を得た。
Example 5 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%. To 95 parts of this chlorinated vinyl chloride resin, 5 parts of a vinyl chloride paste resin obtained by emulsion polymerization having a degree of polymerization of 1400 and a particle diameter of 37 μm after spray drying, MBS (B5 manufactured by Kaneguchi Chemical Co., Ltd.)
61) Add 6 parts and 3 parts of chlorinated polyethylene having a chlorine content of 35%, further add 3 parts of octyltin mercapto as a stabilizer, 2 parts of polyethylene wax as a lubricant, 5 parts of titanium dioxide as a filler, and a yellow colorant 0.00
8 parts were added. The mixture was heated to 130 ° C. in a 300 liter super mixer and blended to obtain a uniform mixture.

【0033】東芝TECコニカル押出機にて、この配合
物を押出成形して1インチ径パイプを製造した。このと
き、ダイ圧力は300kg/cm2であり、吐出量は69kg
/hrであった。JIS−K−7111に準じて、23℃
および0℃でこのパイプのシャルピー衝撃強度を測定し
たところ、それぞれ33kg・cm/cm2および21kg・cm
/cm2であった。JIS−K−7206に準じて、この
パイプの1kg荷重でのビカット軟化点を調べたところ、
127.0℃であった。また、JIS−K−7113に
準じて、23℃で引張試験をおこなったところ、最大抗
張力は568kg/cm2、破断時伸びは120%であっ
た。パイプの表面は目視で赤みがなく、極めて平滑であ
り(AA)、熱安定性および表面性が良好と考えられ
る。
This composition was extruded with a Toshiba TEC conical extruder to produce a 1-inch diameter pipe. At this time, the die pressure was 300 kg / cm 2 and the discharge amount was 69 kg.
/ Hr. 23 ° C according to JIS-K-7111
And 0 ° C., the Charpy impact strength of this pipe was measured to be 33 kg · cm / cm 2 and 21 kg · cm 2 , respectively.
/ Cm 2 . According to JIS-K-7206, when the Vicat softening point of this pipe at a load of 1 kg was examined,
127.0 ° C. When a tensile test was performed at 23 ° C. in accordance with JIS-K-7113, the maximum tensile strength was 568 kg / cm 2 and the elongation at break was 120%. The surface of the pipe has no visual redness, is extremely smooth (AA), and is considered to have good thermal stability and surface properties.

【0034】実施例6 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95部に、重合度が1400で噴霧乾燥
後の粒子径が37μmである、乳化重合で得た塩化ビニ
ル系ペースト樹脂5部、MBS(鐘淵化学工業社製B2
2)8部、および塩素含有量35%の塩素化ポリエチレ
ン3部を加え、更に安定剤としてオクチル錫メルカプト
3部、滑剤としてポリエチレンワックス2部、充填剤と
して二酸化チタン5部、および黄色着色剤0.008部
を加えた。この混合物を、300リットルのスーパーミ
キサーにて130℃まで昇温してブレンドして、均一な
配合物を得た。
Example 6 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%. To 95 parts of this chlorinated vinyl chloride resin, 5 parts of a vinyl chloride paste resin obtained by emulsion polymerization having a degree of polymerization of 1400 and a particle diameter of 37 μm after spray drying, MBS (B2 manufactured by Kaneguchi Chemical Co., Ltd.)
2) 8 parts and 3 parts of chlorinated polyethylene having a chlorine content of 35% were added, and 3 parts of octyltin mercapto as a stabilizer, 2 parts of polyethylene wax as a lubricant, 5 parts of titanium dioxide as a filler, and 0 parts of a yellow colorant were added. .008 parts were added. The mixture was heated to 130 ° C. in a 300 liter super mixer and blended to obtain a uniform mixture.

【0035】東芝製TECコニカル押出機にて、この配
合物を押出成形して1インチ径パイプ押出を製造した。
このとき、ダイ圧力は300kg/cm2であり、吐出量は
72kg/hrであった。JIS−K−7111に準じて、
23℃および0℃でこのパイプのシャルピー衝撃強度を
測定したところ、それぞれ34kg・cm/cm2および22k
g・cm/cm2であった。JIS−K−7206に準じて、
このパイプの1kg荷重でのビカット軟化点を調べたとこ
ろ、127.0℃であった。また、JIS−K−711
3に準じて、23℃で引張試験をおこなったところ、最
大抗張力は560kg/cm2、破断時伸びは120%であ
った。パイプの表面は目視で赤みがなく、極めて平滑で
あり(AA)、熱安定および表面性が良好と考えられ
る。
This compound was extruded with a TEC conical extruder manufactured by Toshiba to produce a 1-inch diameter pipe extrusion.
At this time, the die pressure was 300 kg / cm 2 and the discharge rate was 72 kg / hr. According to JIS-K-7111,
When the Charpy impact strength of this pipe was measured at 23 ° C. and 0 ° C., it was 34 kg · cm / cm 2 and 22 k, respectively.
g · cm / cm 2 . According to JIS-K-7206,
When the Vicat softening point of this pipe at a load of 1 kg was examined, it was 127.0 ° C. Also, JIS-K-711
When a tensile test was conducted at 23 ° C. according to No. 3, the maximum tensile strength was 560 kg / cm 2 and the elongation at break was 120%. The surface of the pipe has no visual redness, is extremely smooth (AA), and is considered to have good thermal stability and surface properties.

【0036】実施例7 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95部に、重合度が1400で噴霧乾燥
後の粒子径が37μmである、乳化重合で得た塩化ビニ
ル系ペースト樹脂5部、MBS(鐘淵化学工業社製B2
2)10部を加え、更に安定剤としてオクチル錫メルカ
プト3部、滑剤としてポリエチレンワックス2部、充填
剤として二酸化チタン5部、および黄色着色剤0.00
8部を加えた。この混合物を、300リットルのスーパ
ーミキサーにて130℃まで昇温してブレンドして、均
一な配合物を得た。
Example 7 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%. To 95 parts of this chlorinated vinyl chloride resin, 5 parts of a vinyl chloride paste resin obtained by emulsion polymerization having a degree of polymerization of 1400 and a particle diameter of 37 μm after spray drying, MBS (B2 manufactured by Kaneguchi Chemical Co., Ltd.)
2) 10 parts were added, 3 parts of octyltin mercapto as a stabilizer, 2 parts of polyethylene wax as a lubricant, 5 parts of titanium dioxide as a filler, and 0.00 of a yellow colorant.
8 parts were added. The mixture was heated to 130 ° C. in a 300 liter super mixer and blended to obtain a uniform mixture.

【0037】東芝製TECコニカル押出機にて、この配
合物を押出成形して1インチ径パイプを製造した。この
とき、ダイ圧力は300kg/cm2であり、吐出量は68k
g/hrであった。JIS−K−7111に準じて、この
パイプの23℃および0℃でのシャルピー衝撃強度を測
定したところ、それぞれ34kg・cm/cm2および22kg
・cm/cm2であった。JIS−K−7206に準じて、
このパイプの1kg荷重でのビカット軟化点を調べたとこ
ろ、127.1℃であった。また、JIS−K−711
3に準じて、23℃で引張試験をおこなったところ、最
大抗張力は574kg/cm2、破断時伸びは114%であ
った。パイプの表面は目視で赤みがなく、極めて平滑で
あり(AA)、熱安定および表面性が良好と考えられ
る。
This compound was extruded with a TEC conical extruder manufactured by Toshiba to produce a 1-inch diameter pipe. At this time, the die pressure is 300 kg / cm 2 and the discharge amount is 68 k / cm 2.
g / hr. When the Charpy impact strength of this pipe at 23 ° C. and 0 ° C. was measured according to JIS-K-7111, it was 34 kg · cm / cm 2 and 22 kg, respectively.
Cm / cm 2 . According to JIS-K-7206,
When the Vicat softening point of this pipe at a load of 1 kg was examined, it was 127.1 ° C. Also, JIS-K-711
When a tensile test was conducted at 23 ° C. according to No. 3, the maximum tensile strength was 574 kg / cm 2 and the elongation at break was 114%. The surface of the pipe has no visual redness, is extremely smooth (AA), and is considered to have good thermal stability and surface properties.

【0038】比較例4 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、MBS(鐘淵化学工業社製
B561)6部および塩素含有量35%の塩素化ポリエ
チレン3部を加え、更に安定剤としてオクチル錫メルカ
プト3部、滑剤としてポリエチレンワックス2部、充填
剤として二酸化チタン5部、および黄色着色剤0.00
8部を加えた。この混合物を、300リットルのスーパ
ーミキサーにて130℃まで昇温してブレンドして、均
一な配合物を得た。
Comparative Example 4 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%. To 100 parts of this chlorinated vinyl chloride resin, 6 parts of MBS (B561 manufactured by Kaneka Chemical Industry Co., Ltd.) and 3 parts of chlorinated polyethylene having a chlorine content of 35% were added, and 3 parts of octyltin mercapto was used as a stabilizer, and polyethylene was used as a lubricant. 2 parts of wax, 5 parts of titanium dioxide as filler, and 0.00 of yellow colorant
8 parts were added. The mixture was heated to 130 ° C. in a 300 liter super mixer and blended to obtain a uniform mixture.

【0039】東芝製TECコニカル押出機にて、この配
合物を押出成形して1インチ径パイプを製造した。この
ときダイ圧力は300kg/cm2であり、吐出量は54kg
/hrであった。JIS−K−7111に準じて、23℃
および0℃でこのパイプのシャルピー衝撃強度を測定し
たところ、それぞれ31kg・cm/cm2および21kg・cm
/cm2であった。JIS−K−7206に準じて、この
パイプの1kg荷重でのビカット軟化点を調べたところ、
127.4℃であった。また、JIS−K−7113に
準じて、23℃で引張試験をおこなったところ、最大抗
張力は560kg/cm2、破断時伸びは125%であっ
た。パイプの表面は、目視で赤みはないが、ざらつき感
があり(A)、熱安定性は良好なものの、表面性が若干
劣っていると考えられる。
This compound was extruded with a TEC conical extruder manufactured by Toshiba to produce a 1-inch diameter pipe. At this time, the die pressure was 300 kg / cm 2 and the discharge amount was 54 kg.
/ Hr. 23 ° C according to JIS-K-7111
When the Charpy impact strength of this pipe was measured at 31 ° C. and 0 ° C., it was 31 kg · cm / cm 2 and 21 kg · cm 2 , respectively.
/ Cm 2 . According to JIS-K-7206, when the Vicat softening point of this pipe at a load of 1 kg was examined,
127.4 ° C. When a tensile test was conducted at 23 ° C. in accordance with JIS-K-7113, the maximum tensile strength was 560 kg / cm 2 and the elongation at break was 125%. The surface of the pipe is not visually reddish, but has a rough feeling (A), and although the thermal stability is good, it is considered that the surface properties are slightly inferior.

【0040】比較例5 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、MBS(鐘淵化学工業社製
B22)8部、および塩素含有量35%の塩素化ポリエ
チレン3部を加え、更に安定剤としてオクチル錫メルカ
プト3部、滑剤としてポリエチレンワックス2部、充填
剤として二酸化チタン5部、および黄色着色剤0.00
8部を加えた。この混合物を、300リットルのスーパ
ーミキサーにて130℃まで昇温してブレンドして、均
一な配合物を得た。
Comparative Example 5 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%. To 100 parts of the chlorinated vinyl chloride resin, 8 parts of MBS (B22 manufactured by Kanegafuchi Chemical Co., Ltd.) and 3 parts of chlorinated polyethylene having a chlorine content of 35% were added, and 3 parts of octyltin mercapto as a stabilizer and 3 parts of a lubricant were added. 2 parts of polyethylene wax, 5 parts of titanium dioxide as filler, and 0.00 of yellow colorant
8 parts were added. The mixture was heated to 130 ° C. in a 300 liter super mixer and blended to obtain a uniform mixture.

【0041】東芝製TECコニカル押出機にて、この配
合物を押出成形して1インチ径パイプを製造した。この
ときダイ圧力は300kg/cm2であり、吐出量は65kg
/hrであった。JIS−K−7111に準じて、23℃
および0℃でこのパイプのシャルピー衝撃強度を測定し
たところ、それぞれ34kg・cm/cm2および23kg・cm
/cm2であった。JIS−K−7206に準じて、この
パイプの1kg荷重でのビカット軟化点を調べたところ、
127.4℃であった。また、JIS−K−7113に
準じて、23℃で引張試験をおこなったところ、最大抗
張力は559kg/cm2、破断時伸びは125%であっ
た。パイプの表面は、目視で赤みはないが、ざらつき感
があり(A)、熱安定性は良好なものの、表面性が若干
劣っていると考えられる。
This compound was extruded with a TEC conical extruder manufactured by Toshiba to produce a 1-inch diameter pipe. At this time, the die pressure was 300 kg / cm 2 and the discharge amount was 65 kg.
/ Hr. 23 ° C according to JIS-K-7111
And 0 ° C., the Charpy impact strength of this pipe was measured to be 34 kg · cm / cm 2 and 23 kg · cm 2 , respectively.
/ Cm 2 . According to JIS-K-7206, when the Vicat softening point of this pipe at a load of 1 kg was examined,
127.4 ° C. When a tensile test was conducted at 23 ° C. according to JIS-K-7113, the maximum tensile strength was 559 kg / cm 2 and the elongation at break was 125%. The surface of the pipe is not visually reddish, but has a rough feeling (A), and although the thermal stability is good, it is considered that the surface properties are slightly inferior.

【0042】比較例6 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、MBS(鐘淵化学工業社製
B22)を10部加え、更に安定剤としてオクチル錫メ
ルカプト3部、滑剤としてポリエチレンワックス2部、
充填剤として二酸化チタン5部、および黄色着色剤
部を加えた。この混合物を、300リットルのスーパー
ミキサーにて130℃まで昇温してブレンドして、均一
な配合物を得た。
Comparative Example 6 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%. To 100 parts of the chlorinated vinyl chloride resin, 10 parts of MBS (manufactured by Kaneka Chemical Industry Co., Ltd.) was added, and 3 parts of octyltin mercapto was used as a stabilizer, and 2 parts of polyethylene wax was used as a lubricant.
5 parts of titanium dioxide as filler and yellow colorant
Parts were added. The mixture was heated to 130 ° C. in a 300 liter super mixer and blended to obtain a uniform mixture.

【0043】東芝製TECコニカル押出機にて、この配
合物を押出成形して1インチ径パイプを製造した。この
ときダイ圧力は300kg/cm2であり、吐出量は52kg
/hrであった。JIS−K−7111に準じて、23℃
および0℃でこのパイプのシャルピー衝撃強度を測定し
たところ、それぞれ32kg・cm/cm2および22kg・cm
/cm2であった。JIS−K−7206に準じて、この
パイプの1kg荷重でのビカット軟化点を調べたところ、
127.1℃であった。また、JIS−K−7113に
準じて、23℃で引張試験をおこなったところ、最大抗
張力は578kg/cm2、破断時伸びは104%であっ
た。パイプの表面は、目視で若干赤みがあり、更に表面
はざらつき感があり(B)、熱安定性および表面性は共
に劣っていると考えられる。
This compound was extruded with a TEC conical extruder manufactured by Toshiba to produce a 1-inch diameter pipe. At this time, the die pressure was 300 kg / cm 2 and the discharge amount was 52 kg.
/ Hr. 23 ° C according to JIS-K-7111
And 0 ° C., the Charpy impact strength of this pipe was measured to be 32 kg · cm / cm 2 and 22 kg · cm 2 , respectively.
/ Cm 2 . According to JIS-K-7206, when the Vicat softening point of this pipe at a load of 1 kg was examined,
127.1 ° C. When a tensile test was performed at 23 ° C. in accordance with JIS-K-7113, the maximum tensile strength was 578 kg / cm 2 and the elongation at break was 104%. The surface of the pipe is slightly reddish visually, and the surface is rough (B), and it is considered that both the thermal stability and the surface properties are inferior.

【0044】理解を容易にする為に、上記実施例および
比較例の内容および結果を表1および2にまとめて示
す。
For easy understanding, the contents and results of the above Examples and Comparative Examples are shown in Tables 1 and 2.

【表1】 [Table 1]

【0045】[0045]

【表2】 [Table 2]

【0046】実施例1〜4の結果から明らかなように、
塩化ビニル系ペースト樹脂を配合した塩素化塩化ビニル
系樹脂組成物は、得られる成形体の衝撃強度を犠牲にせ
ずに、流動性を向上させることがわかる。実施例5〜7
の結果から明らかなように、塩化ビニル系ペースト樹脂
を配合した塩素化塩化ビニル系樹脂組成物は、パイプ押
出において衝撃強度、引張試験、耐熱性を犠牲にせず
に、吐出量を顕著に上げることができ、しかも表面性が
優れたパイプを製造することができる。
As is clear from the results of Examples 1 to 4,
It can be seen that the chlorinated vinyl chloride-based resin composition containing the vinyl chloride-based paste resin improves the fluidity without sacrificing the impact strength of the obtained molded article. Examples 5 to 7
As is clear from the results, the chlorinated vinyl chloride resin composition containing the vinyl chloride paste resin can significantly increase the discharge rate without sacrificing impact strength, tensile test, heat resistance in pipe extrusion. Thus, a pipe having excellent surface properties can be manufactured.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI (C08L 27/24 27:06 51:04) ──────────────────────────────────────────────────の Continued on front page (51) Int.Cl. 6 Identification code FI (C08L 27/24 27:06 51:04)

Claims (5)

【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80〜99重量部、および乳化重合または微
細懸濁重合で製造された、噴霧乾燥後の粒子径が5〜1
00μmであり、重合度が600〜2100である塩化
ビニル系ペースト樹脂1〜20重量部を含む樹脂成分1
00重量部、並びに衝撃吸収剤を3〜15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 before chlorination of 600 to 1500 and a chlorination degree of 62 to 70% by weight, and 80 to 99 parts by weight, and emulsion polymerization or fine suspension polymerization. The manufactured particle diameter after spray drying is 5-1
Resin component 1 containing 1 to 20 parts by weight of a vinyl chloride paste resin having a polymerization degree of 600 to 2100
A chlorinated vinyl chloride resin composition comprising 00 parts by weight and 3 to 15 parts by weight of a shock absorber.
【請求項2】 塩素化塩化ビニル系樹脂の量は少なくと
も90重量部であり、塩化ビニル系ペースト樹脂の量は
10重量部以下である請求項1に記載の塩素化塩化ビニ
ル系樹脂組成物。
2. The chlorinated vinyl chloride resin composition according to claim 1, wherein the amount of the chlorinated vinyl chloride resin is at least 90 parts by weight and the amount of the vinyl chloride paste resin is 10 parts by weight or less.
【請求項3】 衝撃吸収剤が、メチルメタクリレート−
ブタジエン−スチレン共重合体4〜12重量部、および
塩素含有量が10〜50重量%である塩素化ポリエチレ
ン1〜5重量部からなる請求項1または2に記載の塩素
化塩化ビニル系樹脂組成物。
3. The method according to claim 1, wherein the shock absorbing agent is methyl methacrylate.
3. The chlorinated vinyl chloride resin composition according to claim 1, comprising 4 to 12 parts by weight of a butadiene-styrene copolymer and 1 to 5 parts by weight of a chlorinated polyethylene having a chlorine content of 10 to 50% by weight. .
【請求項4】 塩素化ポリエチレンが、30〜40重量
%の塩素含有量を有する請求項3に記載の塩素化塩化ビ
ニル系樹脂組成物。
4. The chlorinated vinyl chloride resin composition according to claim 3, wherein the chlorinated polyethylene has a chlorine content of 30 to 40% by weight.
【請求項5】 衝撃吸収剤が、メチルメタクリレート−
ブタジエン−スチレン共重合体のみからなる請求項1ま
たは2に記載の塩素化塩化ビニル系樹脂組成物。
5. The method according to claim 1, wherein the shock absorber comprises methyl methacrylate.
The chlorinated vinyl chloride resin composition according to claim 1, comprising only a butadiene-styrene copolymer.
JP9356873A 1997-12-25 1997-12-25 Chlorinated vinyl chloride-based resin composition Pending JPH11181206A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9356873A JPH11181206A (en) 1997-12-25 1997-12-25 Chlorinated vinyl chloride-based resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9356873A JPH11181206A (en) 1997-12-25 1997-12-25 Chlorinated vinyl chloride-based resin composition

Publications (1)

Publication Number Publication Date
JPH11181206A true JPH11181206A (en) 1999-07-06

Family

ID=18451192

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9356873A Pending JPH11181206A (en) 1997-12-25 1997-12-25 Chlorinated vinyl chloride-based resin composition

Country Status (1)

Country Link
JP (1) JPH11181206A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000080230A (en) * 1998-09-04 2000-03-21 Takiron Co Ltd Flame-retardant vinyl chloride resin molded form
JP2000186113A (en) * 1998-08-24 2000-07-04 Sekisui Chem Co Ltd Molded article of heat resistant polyvinyl chloride based resin and pipe comprising heat resistant polyvinyl chloride based resin
JP2001139747A (en) * 1999-11-12 2001-05-22 Kanegafuchi Chem Ind Co Ltd Chlorinated vinyl chloride-based resin composition
JP2002284950A (en) * 2001-03-26 2002-10-03 Sekisui Chem Co Ltd Vinyl chloride-base resin composition
JP2002284947A (en) * 2001-03-26 2002-10-03 Sekisui Chem Co Ltd Vinyl chloride-based resin composition
EP3470609A1 (en) * 2017-10-13 2019-04-17 Shin-Etsu Chemical Co., Ltd. Polyvinyl chloride-based resin molded product and method for manufacturing the same

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000186113A (en) * 1998-08-24 2000-07-04 Sekisui Chem Co Ltd Molded article of heat resistant polyvinyl chloride based resin and pipe comprising heat resistant polyvinyl chloride based resin
JP2000080230A (en) * 1998-09-04 2000-03-21 Takiron Co Ltd Flame-retardant vinyl chloride resin molded form
JP2001139747A (en) * 1999-11-12 2001-05-22 Kanegafuchi Chem Ind Co Ltd Chlorinated vinyl chloride-based resin composition
JP2002284950A (en) * 2001-03-26 2002-10-03 Sekisui Chem Co Ltd Vinyl chloride-base resin composition
JP2002284947A (en) * 2001-03-26 2002-10-03 Sekisui Chem Co Ltd Vinyl chloride-based resin composition
JP4555494B2 (en) * 2001-03-26 2010-09-29 積水化学工業株式会社 Vinyl chloride resin composition
EP3470609A1 (en) * 2017-10-13 2019-04-17 Shin-Etsu Chemical Co., Ltd. Polyvinyl chloride-based resin molded product and method for manufacturing the same
JP2019073585A (en) * 2017-10-13 2019-05-16 信越化学工業株式会社 Polyvinyl chloride resin molding and method for producing the same
JP2021191875A (en) * 2017-10-13 2021-12-16 信越化学工業株式会社 Polyvinyl chloride-based resin molding and method for manufacturing the same
US11613639B2 (en) 2017-10-13 2023-03-28 Shin-Etsu Chemical Co., Ltd. Polyvinyl chloride-based resin molded product and method for manufacturing the same

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