JP2001131374A - Chlorinated vinyl chloride resin composition - Google Patents
Chlorinated vinyl chloride resin compositionInfo
- Publication number
- JP2001131374A JP2001131374A JP31479599A JP31479599A JP2001131374A JP 2001131374 A JP2001131374 A JP 2001131374A JP 31479599 A JP31479599 A JP 31479599A JP 31479599 A JP31479599 A JP 31479599A JP 2001131374 A JP2001131374 A JP 2001131374A
- Authority
- JP
- Japan
- Prior art keywords
- vinyl chloride
- chloride resin
- chlorinated
- chlorinated vinyl
- parts
- 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.)
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
(57)【要約】
【課題】 衝撃強度の低下がなく、金属剥離性が向上
し、かつ成形時の熱安定性が改良された塩素化塩化ビニ
ル系樹脂組成物を提供する。
【解決手段】 塩素化塩化ビニル系樹脂100重量部に
対して、塩素化ポリプロピレン樹脂0.1〜3重量部を
含有し、さらに熱安定剤、衝撃吸収剤および滑剤を含有
する塩素化塩化ビニル樹脂組成物にする。PROBLEM TO BE SOLVED: To provide a chlorinated vinyl chloride-based resin composition which does not reduce impact strength, improves metal peelability, and has improved thermal stability during molding. A chlorinated vinyl chloride resin containing 0.1 to 3 parts by weight of a chlorinated polypropylene resin with respect to 100 parts by weight of a chlorinated vinyl chloride resin, and further containing a heat stabilizer, an impact absorber and a lubricant. Into a composition.
Description
【0001】[0001]
【発明の属する技術分野】本発明は、衝撃強度の低下が
なく、金属剥離性が向上し、かつ成形時の熱安定性が改
良さ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 which does not reduce impact strength, has improved metal releasability, and has improved thermal stability during molding.
【0002】[0002]
【従来の技術および発明が解決しようとする課題】塩素
化塩化ビニル系樹脂の成形物は、熱変形温度が高いとい
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。たとえば、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
が用いられている。加えて、パイプを成形する場合に、
塩素化塩化ビニル系樹脂は汎用の塩化ビニル系樹脂用の
押出成形機によって成形することができ、このことも塩
素化塩化ビニル系樹脂を広く使用しやすくする要因とな
っている。2. Description of the Related Art A molded article of a chlorinated vinyl chloride resin has a characteristic that its heat deformation temperature is high. It is used for applications at relatively high temperatures where it cannot be used. 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 addition, when molding pipes,
The chlorinated vinyl chloride-based resin can be molded by a general-purpose vinyl chloride-based resin extrusion molding machine, which also 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
脂に比べて溶融粘度が高く、成形温度での熱安定性が劣
り、成形加工中に焼けやすく押出生産性が低いという欠
点をもっている。たとえば、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、ダイス内で粘着が起こ
りプレートアウト物の発生がおこったり、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
して使えないなどの問題を生ずることがある。On the other hand, when molding a chlorinated vinyl chloride resin, the chlorinated vinyl chloride resin has a higher melt viscosity than the vinyl chloride resin, has poor thermal stability at a molding temperature, and suffers from burning during molding. It has the drawback of being easily extruded and having low extrusion productivity. For example, when extruding a chlorinated vinyl chloride resin into a hot water pipe, sticking occurs in the die and plate-outs occur, coloring occurs, and in some cases, burning occurs during extrusion molding, There may be problems such as being unusable as a product.
【0004】[0004]
【課題を解決するための手段】本発明は、衝撃強度の低
下がなく、金属剥離性が向上し、かつ成形時の熱安定性
を改良した塩素化塩化ビニル系樹脂組成物を提供するた
めになされたものであり、塩素化塩化ビニル系樹脂10
0重量部(以下、部という)に対して、塩素化ポリプロ
ピレン樹脂0.1〜3部を含有し、さらに熱安定剤、衝
撃吸収剤および滑剤を含有する塩素化塩化ビニル系樹脂
組成物(請求項1)、前記塩素化ポリプロピレン樹脂
が、塩素含有率1〜50重量%(以下、%という)で、
かつ10%トルエン溶液にしたときの粘度が0.05〜
10ポイズである請求項1記載の組成物(請求項2)、
および前記塩素化ポリプロピレン樹脂が、塩素含有率2
0〜40%である請求項1または2記載の組成物(請求
項3)に関する。SUMMARY OF THE INVENTION The present invention is to provide a chlorinated vinyl chloride resin composition which does not decrease impact strength, improves metal releasability, and has improved thermal stability during molding. Chlorinated vinyl chloride resin 10
A chlorinated vinyl chloride resin composition containing 0.1 to 3 parts of a chlorinated polypropylene resin with respect to 0 parts by weight (hereinafter referred to as "parts"), and further containing a heat stabilizer, an impact absorber and a lubricant. Item 1), wherein the chlorinated polypropylene resin has a chlorine content of 1 to 50% by weight (hereinafter, referred to as%);
And a viscosity of 0.05% when made into a 10% toluene solution.
The composition according to claim 1, which has 10 poises (claim 2).
And the chlorinated polypropylene resin has a chlorine content of 2
The composition according to claim 1 or 2 (claim 3), which is 0 to 40%.
【0005】[0005]
【発明の実施の形態】本発明に用いられる塩素化塩化ビ
ニル系樹脂は、一般にパイプ押出成形に用いられるもの
であって、塩素化前の塩化ビニル系樹脂の平均重合度
は、600〜1500、さらには600〜1300、と
くには600〜1200であることが好ましい。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未満の場合、充分な機械的強度が得られ
にくくなり、一方、その重合度が1500をこえる場
合、樹脂組成物の加工が容易でなくなる傾向が生ずる。BEST MODE FOR CARRYING OUT THE INVENTION The chlorinated vinyl chloride resin used in the present invention is generally used for pipe extrusion molding. The average degree of polymerization of the vinyl chloride resin before chlorination is 600 to 1500, Further, it is preferably from 600 to 1300, particularly preferably from 600 to 1200. When the average degree of polymerization of the vinyl chloride resin as a raw material of the chlorinated vinyl chloride resin is less than 600, it is difficult to obtain sufficient mechanical strength. On the other hand, when the degree of polymerization exceeds 1500, Processing tends to be difficult.
【0006】前記塩化ビニル系樹脂とは、塩化ビニル単
位70〜100%と塩化ビニルと共重合可能な単量体単
位0〜30%とからなる(共)重合体のことであり、そ
の具体例としては、たとえば塩化ビニルの単独重合体、
塩化ビニルとこれと共重合可能な単量体(たとえばエチ
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
ルなどの1種以上)との共重合体があげられるが、これ
らに限定されるものではない。The vinyl chloride resin is a (co) polymer composed of 70 to 100% of vinyl chloride units and 0 to 30% of monomer units copolymerizable with vinyl chloride. As, for example, a homopolymer of vinyl chloride,
Copolymers of vinyl chloride with a monomer copolymerizable therewith (for example, at least one kind of ethylene, propylene, vinyl acetate, allyl chloride, allyl glycidyl ether, acrylate, vinyl ether, etc.) are mentioned. However, the present invention is not limited to this.
【0007】前記塩素化塩化ビニル系樹脂の塩素化度は
62〜70%、さらには64〜70%であるのが好まし
い。塩素化塩化ビニル系樹脂の塩素化度が62%未満の
場合、充分な熱変形温度を有する組成物が得られにく
く、一方、塩素化度が70%をこえる場合、溶融粘度が
高くなり、樹脂組成物の加工が容易でなくなる傾向が生
ずる。The degree of chlorination of the chlorinated vinyl chloride resin is preferably 62 to 70%, more preferably 64 to 70%. When the degree of chlorination of the chlorinated vinyl chloride resin is less than 62%, it is difficult to obtain a composition having a sufficient heat distortion temperature. On the other hand, when the degree of chlorination exceeds 70%, the melt viscosity increases, There is a tendency for the composition to be difficult to process.
【0008】本発明に用いられる塩素化ポリプロピレン
樹脂は、塩素含有率が1〜50%、さらに20〜40%
で、かつ10%トルエン溶液にしたときの粘度が0.0
5〜10ポイズ(25℃)のものが好ましい。塩素化ポ
リプロピレン樹脂の塩素含有率が50%より多い場合、
塩素化塩化ビニル系樹脂との相溶性が高くなりすぎて成
形時の金属剥離性が充分向上せず、成形時の熱安定性が
充分改良されなくなる傾向が生ずる。一方、塩素含有率
が1%より少ない場合、金属剥離性が向上し、成形時の
熱安定性は改良されるが、衝撃強度の低下を惹き起こす
場合がある。また、前記塩素化ポリプロピレン樹脂は、
10%トルエン溶液にしたときの25℃での粘度が10
ポイズより高い場合、塩素化塩化ビニル系樹脂への分散
が不均一になり、成形時の収縮が大きく、成形体の外観
を損う場合がある。逆に、0.05ポイズ未満の場合、
分子量が低いため金属剥離性効果が発現しなかったり熱
安定性が低くなったりする傾向が生ずる。The chlorinated polypropylene resin used in the present invention has a chlorine content of 1 to 50%, more preferably 20 to 40%.
And 10% toluene solution has a viscosity of 0.0
Those having 5 to 10 poise (25 ° C.) are preferred. When the chlorine content of the chlorinated polypropylene resin is more than 50%,
The compatibility with the chlorinated vinyl chloride resin becomes so high that the metal releasability at the time of molding is not sufficiently improved, and the thermal stability at the time of molding tends to be not sufficiently improved. On the other hand, when the chlorine content is less than 1%, the metal releasability is improved and the thermal stability at the time of molding is improved, but the impact strength may be reduced. Further, the chlorinated polypropylene resin,
The viscosity at 25 ° C. of a 10% toluene solution becomes 10%.
When the poise is higher than the poise, the dispersion in the chlorinated vinyl chloride resin becomes uneven, the shrinkage during molding is large, and the appearance of the molded article may be impaired. Conversely, if less than 0.05 poise,
Since the molecular weight is low, there is a tendency that the metal peeling effect is not exhibited or the thermal stability is lowered.
【0009】前記塩素化ポリプロピレン樹脂の使用量
は、塩素化塩化ビニル系樹脂100部に対して0.1〜
3部である。使用量が0.1部未満の場合、期待する効
果が得られない。一方、3部より多い場合、相分離がお
こり、製品の品質が低下したり外観を損うようになる。The chlorinated polypropylene resin is used in an amount of 0.1 to 100 parts per 100 parts of the chlorinated vinyl chloride resin.
It is three parts. If the amount used is less than 0.1 part, the expected effect cannot be obtained. On the other hand, if the amount is more than 3 parts, phase separation occurs, and the quality of the product is deteriorated or the appearance is impaired.
【0010】本発明に用いられる熱安定剤は、組成物の
熱安定性を改善し、成形加工中に焼けやすく、押出生産
性が低下するのを改善するために使用される。The heat stabilizer used in the present invention is used for improving the heat stability of the composition, improving the ease of burning during molding and reducing the decrease in extrusion productivity.
【0011】前記熱安定剤の具体例としては、たとえば
Ba−Zn系安定剤、Ca−Zn系安定剤、Sn系安定
剤、Pb系安定剤、Mg−Al系安定剤、ハイドロタル
サイト系安定剤など、通常使用される熱安定剤があげら
れる。これらは単独で用いてもよく2種以上を組み合わ
せて用いてもよい。Specific examples of the heat stabilizer include, for example, Ba-Zn stabilizer, Ca-Zn stabilizer, Sn stabilizer, Pb stabilizer, Mg-Al stabilizer, hydrotalcite stabilizer. And heat stabilizers that are commonly used, such as agents. These may be used alone or in combination of two or more.
【0012】前記熱安定剤の使用量は、塩素化塩化ビニ
ル系樹脂100部に対して0.1〜7部、さらには0.
5〜5部であるのが好ましい。The heat stabilizer is used in an amount of 0.1 to 7 parts, more preferably 0.1 to 7 parts, per 100 parts of the chlorinated vinyl chloride resin.
It is preferably 5 to 5 parts.
【0013】本発明に用いられる衝撃吸収剤としては、
通常、塩素化塩化ビニル系樹脂の衝撃吸収剤として用い
られているもの、たとえばメタクリル酸メチル−ブタジ
エン−スチレン系重合体(MBS)、アクリロニトリル
−ブタジエン−スチレン系重合体(ABS)、ブタジエ
ンまたはスチレン−ブタジエンゴムにメチルメタクリレ
ート−スチレン−アクリロニトリルをグラフトした重合
体(MABS)、塩素化ポリエチレン(CPE)、アク
リルゴムを主成分とした耐衝撃吸収剤などであれば使用
することができる。これらは単独で用いてもよく、2種
以上を組み合わせて用いてもよい。これらのうちではM
BSとCPEの併用が好ましい。The shock absorber used in the present invention includes:
Those usually used as impact absorbers for chlorinated vinyl chloride resins, for example, methyl methacrylate-butadiene-styrene polymer (MBS), acrylonitrile-butadiene-styrene polymer (ABS), butadiene or styrene- Any polymer such as a polymer obtained by grafting butadiene rubber with methyl methacrylate-styrene-acrylonitrile (MABS), chlorinated polyethylene (CPE), or an impact rubber containing acrylic rubber as a main component can be used. These may be used alone or in combination of two or more. Of these, M
A combination of BS and CPE is preferred.
【0014】前記衝撃吸収剤の使用量は、耐衝撃性と熱
変形温度のバランスをもたせる点から、塩素化塩化ビニ
ル系樹脂100部あたり4〜15部、さらには6〜9部
であるのが好ましい。また、塩素化ポリプロピレン樹脂
の添加効果をさらに向上させるためには、塩素化ポリエ
チレンを0.1〜3部併用するのが好ましい。The amount of the shock absorber used is preferably 4 to 15 parts, more preferably 6 to 9 parts per 100 parts of the chlorinated vinyl chloride resin, from the viewpoint of providing a balance between impact resistance and heat distortion temperature. preferable. In order to further improve the effect of adding the chlorinated polypropylene resin, it is preferable to use 0.1 to 3 parts of chlorinated polyethylene in combination.
【0015】本発明に用いられる滑剤としては、ポリエ
チレンワックス、酸化ポリエチレン、高分子量パラフィ
ンワックスなどがあげられる。これらは単独で用いても
よく、2種以上を組み合わせて用いてもよい。なかでも
ポリエチレンワックスが好ましい。The lubricant used in the present invention includes polyethylene wax, polyethylene oxide, high molecular weight paraffin wax and the like. These may be used alone or in combination of two or more. Among them, polyethylene wax is preferred.
【0016】前記滑剤の使用量は、塩素化塩化ビニル系
樹脂100部に対して1.5〜4部であるのが好まし
い。滑剤の配合量が1.5部未満の場合、溶融粘度が高
くなるため、押出加工性が低下する傾向が生じ、4部を
こえる場合、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が生じやすくなる。The amount of the lubricant is preferably 1.5 to 4 parts based on 100 parts of the chlorinated vinyl chloride resin. If the blending amount of the lubricant is less than 1.5 parts, the melt viscosity becomes high, and the extrusion processability tends to decrease. If it exceeds 4 parts, the lubricity between the resin and the metal becomes too strong, and the extrusion process is performed. Pulsation is likely to occur in the resin discharge at the time.
【0017】本発明では、塩素化塩化ビニル系樹脂、塩
素化ポリプロピレン樹脂、熱安定剤、衝撃吸収剤および
滑剤からなる必須成分に、さらに改質剤、加工助剤など
の塩化ビニル系樹脂に使用する添加剤を添加してもよ
い。また、二酸化チタンや炭酸カルシウムなどの充填剤
を添加してもよい。さらに、着色剤として塩素化塩化ビ
ニル系樹脂の成形加工に一般に用いられるものを添加し
てもよい。In the present invention, it is used as an essential component comprising a chlorinated vinyl chloride resin, a chlorinated polypropylene resin, a heat stabilizer, a shock absorber and a lubricant, and further as a vinyl chloride resin such as a modifier and a processing aid. May be added. Further, a filler such as titanium dioxide or calcium carbonate may be added. Further, a coloring agent that is generally used for molding a chlorinated vinyl chloride resin may be added.
【0018】本発明の塩素化塩化ビニル系樹脂組成物
は、前記の必須成分および所望の添加剤を、従来の混合
・混練装置を用いて配合することにより製造することが
できる。本発明の塩素化塩化ビニル系樹脂組成物は、従
来の塩素化塩化ビニル系樹脂(組成物)が用いられてい
る分野で用いることができるが、前記のような特性か
ら、押出パイプの成形にとくに好ましく用いられる。The chlorinated vinyl chloride resin composition of the present invention can be produced by blending the above essential components and desired additives using a conventional mixing / kneading apparatus. The chlorinated vinyl chloride resin composition of the present invention can be used in the field where a conventional chlorinated vinyl chloride resin (composition) is used. Particularly preferably used.
【0019】[0019]
【実施例】以下に、本発明の組成物を実施例をあげてさ
らに詳しく説明するが、本発明はこれらに限定されるも
のではない。The composition of the present invention will be described below in more detail with reference to examples, but the present invention is not limited to these examples.
【0020】なお、実施例および比較例で用いる原材料
および評価方法を以下にまとめて説明する。The raw materials and evaluation methods used in the examples and comparative examples are described below.
【0021】[原材料] 塩素化塩化ビニル樹脂:H829(鐘淵化学工業(株)
製、塩素化度68%、平均重合度1000) 塩素化ポリプロピレン樹脂1:16−LP(東洋化成工
業(株)製、塩素化ポリプロピレン、塩素含有率32
%、10%トルエン溶液粘度約0.4P(25℃)) 熱安定剤:ジオクチル錫メルカプト(日東化成(株)
製、TVS#8831) 衝撃吸収剤1:B56(鐘淵化学工業(株)製、MB
S) 衝撃吸収剤2:H135(ダイソー(株)製、塩素化ポ
リエチレン) 滑剤1:AC629A(アライド・シグナル社製、ポリ
エチレンワックス) 滑剤2:AC617A(アライド・シグナル社製、ポリ
エチレンワックス) 充填剤:R650(堺化学工業(株)製、酸化チタン)[Raw materials] Chlorinated vinyl chloride resin: H829 (Kanebuchi Chemical Industry Co., Ltd.)
Chlorinated polypropylene resin 1: 16-LP (manufactured by Toyo Kasei Kogyo Co., Ltd., chlorinated polypropylene, chlorine content 32)
%, 10% toluene solution viscosity about 0.4P (25 ° C)) Thermal stabilizer: dioctyltin mercapto (Nitto Kasei Co., Ltd.)
Shock absorber 1: B56 (manufactured by Kanegafuchi Chemical Industry Co., Ltd., MB)
S) Shock absorber 2: H135 (chlorinated polyethylene manufactured by Daiso Corporation) Lubricant 1: AC629A (polyethylene wax manufactured by Allied Signal) Lubricant 2: AC617A (polyethylene wax manufactured by Allied Signal) Filler: R650 (made by Sakai Chemical Industry Co., Ltd., titanium oxide)
【0022】[評価方法] (プレートアウト物発生時間および表面性)東洋精機
(株)製プラストグラフのラボコニカル押出実験機を用
いて、バレル温度190℃、ダイス温度205℃、スク
リュー回転数30回転の条件で丸棒の成形体を押し出し
た。押し出した丸棒の表面性の外観評価(目視)とダイ
先端に発生する黒化したプレートアウト物の発生時間を
測定した。[Evaluation Method] (Plate-out occurrence time and surface properties) Using a lab conical extrusion tester manufactured by Toyo Seiki Co., Ltd., a barrel temperature of 190 ° C., a die temperature of 205 ° C., and a screw rotation number of 30 were used. Under the conditions, a round bar was extruded. The appearance of the extruded round bars was evaluated for appearance (visual observation), and the time of occurrence of blackened plate-outs generated at the tip of the die was measured.
【0023】なお、外観評価(目視)は、丸棒でプレー
トアウト物が発生する前のサンプルで評価し、◎:優、
○:良、△:可、×:不可とした。In addition, the appearance evaluation (visual) was evaluated on a sample before a plate-out object was generated with a round bar.
:: good, Δ: acceptable, ×: unacceptable.
【0024】(アイゾット衝撃値)樹脂組成物を8イン
チロールで混練したのち、プレス加工を行ない、JIS
K7110のアイゾット衝撃試験を実施した。サンプル
作成条件はロール混練を200℃で5分、プレス加工を
205℃で10分とした。(Izod impact value) After kneading the resin composition with an 8-inch roll, press processing is performed, and JIS
An Izod impact test of K7110 was performed. The sample preparation conditions were as follows: roll kneading at 200 ° C. for 5 minutes and press working at 205 ° C. for 10 minutes.
【0025】評価は、サンプル厚さ5mm、Vノッチ、
3.92J(40kg・cm)ハンマーを用いて行なっ
た。The evaluation was performed with a sample thickness of 5 mm, a V notch,
The test was performed using a 3.92 J (40 kg · cm) hammer.
【0026】実施例1〜3および比較例1 表1に示す成分を表1に示す量配合し、ホモジナイザー
により均一に混合して樹脂組成物を製造した。得られた
樹脂組成物を用いて試験用サンプルを作成し、評価し
た。結果を表1に示す。Examples 1 to 3 and Comparative Example 1 The components shown in Table 1 were mixed in the amounts shown in Table 1, and uniformly mixed with a homogenizer to produce a resin composition. A test sample was prepared using the obtained resin composition and evaluated. Table 1 shows the results.
【0027】[0027]
【表1】 [Table 1]
【0028】表1から、塩素化ポリプロピレン樹脂を添
加しても衝撃強度の低下は見られず、また、ラボコニカ
ルの丸棒押出評価で、プレートアウト物発生時間が向上
したり、丸棒表面の表面性が良好になることがわかる。From Table 1, it can be seen that even when the chlorinated polypropylene resin was added, no drop in impact strength was observed, and in the evaluation of round bar extrusion by Labo Conical, the time required to generate plate-outs was improved, and the surface of the round bar surface was improved. It turns out that the property becomes good.
【0029】[0029]
【発明の効果】本発明の塩素化塩化ビニル系樹脂組成物
を用いることにより、衝撃強度の低下がなく、金属剥離
性が向上し、かつ成形時の熱安定性が改良され、押出成
形時のプレートアウト物の発生を抑制することが可能と
なり、パイプ押出などの成形加工における連続生産性が
飛躍的に向上する。EFFECT OF THE INVENTION By using the chlorinated vinyl chloride resin composition of the present invention, impact strength is not reduced, metal releasability is improved, thermal stability during molding is improved, and extrusion molding is improved. The occurrence of plate-outs can be suppressed, and the continuous productivity in molding processes such as pipe extrusion is dramatically improved.
Claims (3)
対して、塩素化ポリプロピレン樹脂0.1〜3重量部を
含有し、さらに熱安定剤、衝撃吸収剤および滑剤を含有
する塩素化塩化ビニル系樹脂組成物。1. A chlorinated vinyl chloride containing 0.1 to 3 parts by weight of a chlorinated polypropylene resin with respect to 100 parts by weight of a chlorinated vinyl chloride resin, and further containing a heat stabilizer, an impact absorber and a lubricant. -Based resin composition.
含有率1〜50重量%で、かつ10重量%トルエン溶液
にしたときの粘度が0.05〜10ポイズである請求項
1記載の組成物。2. The composition according to claim 1, wherein the chlorinated polypropylene resin has a chlorine content of 1 to 50% by weight and a viscosity in a 10% by weight toluene solution of 0.05 to 10 poise.
含有率20〜40重量%である請求項1または2記載の
組成物。3. The composition according to claim 1, wherein the chlorinated polypropylene resin has a chlorine content of 20 to 40% by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP31479599A JP2001131374A (en) | 1999-11-05 | 1999-11-05 | Chlorinated vinyl chloride resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP31479599A JP2001131374A (en) | 1999-11-05 | 1999-11-05 | Chlorinated vinyl chloride resin composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2001131374A true JP2001131374A (en) | 2001-05-15 |
Family
ID=18057702
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP31479599A Pending JP2001131374A (en) | 1999-11-05 | 1999-11-05 | Chlorinated vinyl chloride resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2001131374A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103265780A (en) * | 2013-05-07 | 2013-08-28 | 上海氯碱化工股份有限公司 | Chlorinated polyvinylchloride mixing material |
| CN103304914A (en) * | 2013-04-23 | 2013-09-18 | 杭州联通管业有限公司 | Super-tough and super-flexible high-temperature-resistance polyvinyl chloride pipe and manufacturing technology thereof |
| CN103509240A (en) * | 2012-06-27 | 2014-01-15 | 合肥杰事杰新材料股份有限公司 | CPVC-PP (Chlorinated Polyvinyl Chloride-Propene Polymer) alloy material and preparation method thereof |
| JP2018059045A (en) * | 2015-10-19 | 2018-04-12 | 三井化学株式会社 | Resin composition, molded article and pipe comprising the composition |
| CN111138784A (en) * | 2019-12-30 | 2020-05-12 | 宜宾天亿新材料科技有限公司 | CPVC prefabricated pipe for biaxial orientation and production method thereof, CPVC-O pipe material and production method thereof |
| JPWO2022202783A1 (en) * | 2021-03-24 | 2022-09-29 |
-
1999
- 1999-11-05 JP JP31479599A patent/JP2001131374A/en active Pending
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103509240A (en) * | 2012-06-27 | 2014-01-15 | 合肥杰事杰新材料股份有限公司 | CPVC-PP (Chlorinated Polyvinyl Chloride-Propene Polymer) alloy material and preparation method thereof |
| CN103304914A (en) * | 2013-04-23 | 2013-09-18 | 杭州联通管业有限公司 | Super-tough and super-flexible high-temperature-resistance polyvinyl chloride pipe and manufacturing technology thereof |
| CN103265780A (en) * | 2013-05-07 | 2013-08-28 | 上海氯碱化工股份有限公司 | Chlorinated polyvinylchloride mixing material |
| JP2018059045A (en) * | 2015-10-19 | 2018-04-12 | 三井化学株式会社 | Resin composition, molded article and pipe comprising the composition |
| CN111138784A (en) * | 2019-12-30 | 2020-05-12 | 宜宾天亿新材料科技有限公司 | CPVC prefabricated pipe for biaxial orientation and production method thereof, CPVC-O pipe material and production method thereof |
| CN111138784B (en) * | 2019-12-30 | 2021-09-28 | 宜宾天亿新材料科技有限公司 | CPVC prefabricated pipe for biaxial orientation and production method thereof, CPVC-O pipe and production method thereof |
| JPWO2022202783A1 (en) * | 2021-03-24 | 2022-09-29 | ||
| WO2022202783A1 (en) * | 2021-03-24 | 2022-09-29 | 株式会社カネカ | Manufacturing method and use for chlorinated polyvinyl chloride resin |
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