JPH11269295A - Chlorinated vinyl chloride based resin composition for foaming - Google Patents

Chlorinated vinyl chloride based resin composition for foaming

Info

Publication number
JPH11269295A
JPH11269295A JP7562698A JP7562698A JPH11269295A JP H11269295 A JPH11269295 A JP H11269295A JP 7562698 A JP7562698 A JP 7562698A JP 7562698 A JP7562698 A JP 7562698A JP H11269295 A JPH11269295 A JP H11269295A
Authority
JP
Japan
Prior art keywords
vinyl chloride
metal
weight
chlorinated vinyl
foaming
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
JP7562698A
Other languages
Japanese (ja)
Inventor
Seiji Tokawa
清司 東川
Teruo Fujimoto
照雄 藤本
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.)
Tokuyama Sekisui Co Ltd
Original Assignee
Tokuyama Sekisui 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 Tokuyama Sekisui Co Ltd filed Critical Tokuyama Sekisui Co Ltd
Priority to JP7562698A priority Critical patent/JPH11269295A/en
Publication of JPH11269295A publication Critical patent/JPH11269295A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To provide a chlorinated vinyl chloride based resin composition for foaming good in foamability and moldability without using any lead based stabilizers and tin based stabilizers. SOLUTION: This chlorinated vinyl chloride based resin composition for foaming comprises 100 pts.wt. chlorinated vinyl chloride resin having an average chlorine content of 60-72 wt.% alone or its mixture of a vinyl chloride resin; 0.5-6 pts.wt. at least one stabilizer selected from silicate salts of a group II or III metal, complexes of silicic acid and an oxide of said metal, complexes of silicic acid and a hydroxide of said metal, complexes of silicic acid and a carbonate of said metal, hydrotalcites and zeolites; 3-20 pts.wt. methacrylic ester based resin; and 0.1-3 pts.wt. decomposition type organic blowing agent.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、耐熱性を有し、発
泡性の優れた塩素化塩化ビニル系樹脂組成物に関する。
TECHNICAL FIELD The present invention relates to a chlorinated vinyl chloride resin composition having heat resistance and excellent foamability.

【0002】[0002]

【従来の技術】塩素化塩化ビニル系樹脂(以下、CPV
Cという)は、一般に塩化ビニル系樹脂(以下、PVC
という)を塩素化して作られる。CPVCはPVCの長
所といわれる難燃性、耐薬品性の特性を残し、かつPV
Cの欠点といわれる耐熱温度が低い点を改良しているの
で広い用途が期待されている。一方PVCは熱変形温度
が低いために、60〜70℃以上では使用できないとい
う大きな欠点をもっている。これに対しCPVCは熱変
形温度がPVCより20〜40℃も高く、PVCの欠点
である耐熱性が改良されている。従って、発泡成形体に
した場合も同様で耐熱性が優れている。
2. Description of the Related Art Chlorinated vinyl chloride resin (hereinafter referred to as CPV)
C) is generally a vinyl chloride resin (hereinafter referred to as PVC).
Chlorination). CPVC retains flame-retardant and chemical-resistant properties, which are said to be advantages of PVC, and
C is expected to be used in a wide range of applications because it has improved the low heat resistance temperature which is said to be a disadvantage of C. On the other hand, PVC has a major drawback that it cannot be used at temperatures of 60 to 70 ° C. or higher because of its low heat deformation temperature. On the other hand, the heat deformation temperature of CPVC is higher by 20 to 40 ° C. than that of PVC, and the heat resistance, which is a drawback of PVC, is improved. Therefore, the heat resistance is excellent in the case of using a foam molded article.

【0003】従来の発泡成形体の安定剤は主に鉛配合や
錫配合が使用されていた。しかし、最近になり脱鉛化の
動きがあり、鉛配合は嫌われ、また錫配合では大きく耐
熱性が損なわれ、また成形が難しく、ロングラン性に乏
しいことから塩素化塩化ビニル系樹脂を使用しての発泡
成形体を得ることは難しかった。
[0003] Conventionally, as a stabilizer for a foamed molded article, a lead compound or a tin compound has been mainly used. However, recently there has been a trend toward de-leading, and the use of chlorinated vinyl chloride resin has been hindered. It was difficult to obtain all the foamed molded articles.

【0004】[0004]

【発明が解決しようとする課題】本発明は、上記問題点
を解決するものであって、CPVCを使用し、鉛系安定
剤、錫系安定剤を使用せず、発泡性、成形性が良好な発
泡用CPVC組成物を提供するものである。
SUMMARY OF THE INVENTION The present invention solves the above-mentioned problems, and uses CPVC, does not use a lead-based stabilizer or a tin-based stabilizer, and has good foamability and moldability. The present invention provides a CPVC composition for foaming.

【0005】[0005]

【課題を解決するための手段】本発明は、平均塩素含有
量が60〜72重量%であるCPVC単体またはPVC
との混合物100重量部、周期律表第II族もしくは第
III族金属のケイ酸塩、ケイ酸と前記金属の酸化物と
の複合物、ハイドロタルサイト類、又はゼオライト類の
うち少なくとも1種以上の安定剤0.5〜6重量部にポ
リメチルメタクリレート樹脂3〜20重量部、分解型有
機発泡剤0.1〜3重量部からなることを特徴とする。
SUMMARY OF THE INVENTION The present invention relates to a method for producing a single CPVC or PVC having an average chlorine content of 60 to 72% by weight.
At least one of a silicate of a metal of Group II or Group III of the periodic table, a composite of silicic acid and an oxide of the metal, a hydrotalcite, or a zeolite Characterized in that the stabilizer comprises 0.5 to 6 parts by weight of a stabilizer, 3 to 20 parts by weight of a polymethyl methacrylate resin, and 0.1 to 3 parts by weight of a decomposable organic foaming agent.

【0006】本発明で使用されるCPVCの平均重合度
は、塩素化前のPVCの平均重合度として500〜14
00が好ましい。平均重合度が500未満では衝撃性が
低下し、1400を超えると溶融流動性が低下し、成形
が困難となるからである。
The average degree of polymerization of CPVC used in the present invention is 500 to 14 as an average degree of polymerization of PVC before chlorination.
00 is preferred. If the average degree of polymerization is less than 500, the impact strength is reduced, and if it exceeds 1400, the melt fluidity is reduced, and molding becomes difficult.

【0007】また、CPVCの平均塩素含有量は60〜
72重量%に限定される。平均塩素含有量が60重量%
未満では耐熱性が低下し変形が発生しやすくなり、72
重量%を超えると流動性が大きく低下し、成形が困難と
なるからである。また、PVCと併用する場合も同様で
60〜72重量%の範囲に限定される。
The average chlorine content of CPVC is 60 to
Limited to 72% by weight. 60% by weight average chlorine content
If it is less than 30, heat resistance is reduced and deformation is apt to occur, and
If the content exceeds% by weight, the fluidity is greatly reduced, and molding becomes difficult. Similarly, when used in combination with PVC, it is limited to the range of 60 to 72% by weight.

【0008】また、本発明で使用される安定剤の周期律
表第II族もしくは第III族金属としてはMg、A
l、Ca、又はZnが好ましい。
The metal used in the present invention may be Mg, A
l, Ca, or Zn is preferred.

【0009】上記ケイ酸塩としては、ケイ酸マグネシウ
ム、ケイ酸カルシウム、ケイ酸バリウム、ケイ酸ストロ
ンチウム等のケイ酸アルカリ土類金属塩;ケイ酸亜鉛等
のケイ酸の第IIb族金属塩;ケイ酸アルミニウム等の
ケイ酸の第IIIb族金属塩が挙げられ、単独で用いら
れてもよく2種以上が併用されてもよい。これらのケイ
酸塩の内でも非鉛系の無毒安定剤として、ケイ酸マグネ
シウム、ケイ酸カルシウム、ケイ酸亜鉛、ケイ酸アルミ
ニウムが好適に使用される。
Examples of the silicate include alkaline earth metal silicates such as magnesium silicate, calcium silicate, barium silicate and strontium silicate; Group IIb metal salts of silicic acid such as zinc silicate; Group IIIb metal salts of silicic acid, such as aluminum silicate, may be used alone or in combination of two or more. Among these silicates, magnesium silicate, calcium silicate, zinc silicate and aluminum silicate are preferably used as a non-lead-based non-toxic stabilizer.

【0010】ケイ酸と前記金属の酸化物、水酸化物、又
は炭酸塩との複合物としては以下に例示するものが挙げ
られるが、これらに限定されるものではない。
Examples of the composite of silicic acid and the oxide, hydroxide, or carbonate of the metal include, but are not limited to, the following.

【0011】上記周期律表の第II族もしくは第II族
金属との酸化物及び水酸化物としては、例えば酸化カル
シウム、水酸化カルシウム、酸化マグネシウム、水酸化
マグネシウム、酸化亜鉛、水酸化亜鉛などが挙げられ
る。
Examples of the oxides and hydroxides of Group II or Group II metals in the above periodic table include calcium oxide, calcium hydroxide, magnesium oxide, magnesium hydroxide, zinc oxide, zinc hydroxide and the like. No.

【0012】上記周期律表の第II族もしくは第III
族金属との炭酸塩としては、例えば塩基性炭酸カルシウ
ム、炭酸カルシウム、塩基性炭酸マグネシウム、炭酸マ
グネシウム、塩基性炭酸亜鉛の他重炭酸塩、例えば重炭
酸カルシウム、重炭酸マグネシウムなどが挙げられる。
Group II or III of the periodic table
Examples of the carbonate with a group metal include basic calcium carbonate, calcium carbonate, basic magnesium carbonate, magnesium carbonate, basic zinc carbonate, and other bicarbonates such as calcium bicarbonate and magnesium bicarbonate.

【0013】上記安定剤の使用量は、樹脂成分100重
量部に対して0.5〜6重量部に限定される。0.5重
量部未満ではCPVC組成物が熱安定性に乏しく、6重
量部を超えるとCPVCの溶融流動性が低下し成形が困
難となる。
The amount of the stabilizer is limited to 0.5 to 6 parts by weight based on 100 parts by weight of the resin component. If the amount is less than 0.5 part by weight, the thermal stability of the CPVC composition is poor, and if it exceeds 6 parts by weight, the melt fluidity of the CPVC is reduced and molding becomes difficult.

【0014】また、本発明ではCPVCにメタクリル酸
エステル系樹脂が加えられる。メタクリル酸エステル系
樹脂としてはメタクリル酸エステルの単独重合体のほ
か、メタクリル酸エステルと他の単量体との共重合体を
も用いることができる。メタクリル酸エステルとして
は、メチルメタクリレート、エチルメタクリレート等が
用いられる。他の単量体としては、エチルアクリレー
ト、アクリルニトリル等が用いられる。上述の共重合体
の中では、メタクリル酸エステルの占める割合が他の単
量体よりも多いことが好ましい。
In the present invention, a methacrylic ester resin is added to CPVC. As the methacrylic acid ester-based resin, a homopolymer of methacrylic acid ester or a copolymer of methacrylic acid ester and another monomer can be used. As the methacrylate, methyl methacrylate, ethyl methacrylate and the like are used. As other monomers, ethyl acrylate, acrylonitrile and the like are used. In the above-mentioned copolymer, it is preferable that the ratio of the methacrylic acid ester is larger than that of the other monomers.

【0015】メタクリル酸エステル系樹脂は、CPVC
100重量部に対し、3〜20重量部に限定され、好ま
しくは5〜13重量部である。このような割合でメタク
リル酸エステル系樹脂を加えると、CPVCは発泡する
に適した溶融粘度をもつに至り、よく発泡して小さな気
泡を生成するとともに、いったん生成した気泡が簡単に
は潰れなくなる。
The methacrylate resin is CPVC
The amount is limited to 3 to 20 parts by weight, preferably 5 to 13 parts by weight, per 100 parts by weight. When the methacrylic acid ester-based resin is added at such a ratio, the CPVC has a melt viscosity suitable for foaming, and foams well to generate small bubbles, and the bubbles once formed cannot be easily collapsed.

【0016】本発明で用いる分解型有機発泡剤としては
アゾジカルボンアミド等の熱分解型有機発泡剤が用いら
れる。添加部数はCPVC100重量部に対し熱分解型
有機発泡剤は0.1〜3重量部に限定され、好ましくは
0.1〜0.5重量部である。
As the decomposable organic foaming agent used in the present invention, a thermally decomposable organic foaming agent such as azodicarbonamide is used. The number of parts to be added is limited to 0.1 to 3 parts by weight, preferably 0.1 to 0.5 parts by weight, of the pyrolytic organic blowing agent based on 100 parts by weight of CPVC.

【0017】本発明に係る組成物は、上記に述べたもの
のほか充填剤として炭酸カルシウム、タルク、クレイ、
シリカ等添加できる。充填剤は、微細な粒子が好まし
く、特に3μm以下の平均粒子径のものが好ましい。
The composition according to the present invention comprises calcium carbonate, talc, clay, as fillers in addition to those described above.
Silica and the like can be added. As the filler, fine particles are preferable, and those having an average particle diameter of 3 μm or less are particularly preferable.

【0018】そのほか、本発明に関わる組成物は、CP
VC加工の際に一般に用いられる衝撃改質剤、滑剤、可
塑剤、酸化防止剤、紫外線吸収剤、着色剤、難燃剤など
を添加することができる。
In addition, the composition according to the present invention comprises CP
An impact modifier, a lubricant, a plasticizer, an antioxidant, an ultraviolet absorber, a colorant, a flame retardant, and the like generally used in VC processing can be added.

【0019】本発明の関わる組成物を作るには、上述の
配合物をスーパーミキサーで均一に混合して配合粉を得
る。また、押出成形し易い形にするには2軸押出機など
でペレット状にするのが好ましい。
In order to prepare the composition according to the present invention, the above-mentioned compound is uniformly mixed with a super mixer to obtain a compounded powder. Further, in order to obtain a shape that can be easily extruded, it is preferable to form a pellet with a twin screw extruder or the like.

【0020】本発明に関わる成形体は、配合粉、または
ペレット化された組成物を押出機に入れ、溶融させて発
泡成形体を得る。本発明のCPVC組成物から得られる
成形品は、例えば住宅用の廻り縁、手摺り、カーテンレ
ール、窓枠等の材料として、様々な塩化ビニル系の発泡
製品に使用できる。
The molded product according to the present invention is obtained by putting a compounded powder or a pelletized composition into an extruder and melting it to obtain a foamed molded product. The molded article obtained from the CPVC composition of the present invention can be used for various vinyl chloride foamed products, for example, as materials for peripheral edges of houses, handrails, curtain rails, window frames, and the like.

【0021】本発明のCPVC組成物は、押出成形法、
射出成形法にて成形可能であるが、押出成形法がより適
している。本発明のCPVC組成物を押出成形を行うに
は、例えば、組成物をスーパーミキサ−で均一に分散し
た混合物、またはこの混合物を押出機に供給しペレタイ
ザ−で切断して得られたペレットを押出成形すればよ
い。
The CPVC composition of the present invention is obtained by an extrusion method,
Although injection molding is possible, extrusion molding is more suitable. In order to extrude the CPVC composition of the present invention, for example, a mixture obtained by uniformly dispersing the composition by a supermixer, or a pellet obtained by supplying the mixture to an extruder and cutting the mixture with a pelletizer, is used. What is necessary is just to shape | mold.

【0022】[0022]

【発明の実施の形態】以下に実施例を掲げて本発明を更
に詳しく説明するが、本発明はこれら実施例のみに限定
されるものではない。
BEST MODE FOR CARRYING OUT THE INVENTION Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples.

【0023】(実施例1〜6、比較例1〜4)表1に示
す配合量の各成分をスーパ−ミキサ−で均一に混合した
樹脂組成物を、シリンダ−温度をそれぞれ(C1:14
0℃、C2:150℃、C3:160℃、C4:165
℃)に設定し、アダプタ−温度160℃、ダイ温度15
5℃に設定した30mm2軸異方向押出機に供給し、ペ
レタイザ−で切断してペレットを得た。次いでペレット
を65mmシングル押出機(L/D=22、フルフライ
トスクリュ−、圧縮比=3.0)でバレル温度をそれぞ
れ(B1:150℃、B2:160℃、B3:170
℃)に設定し、ダイ温度をそれぞれ(DH:175℃、
D1:175℃、D2:185℃)に設定した条件で押
出成形し、平板状の成形体を得た。
(Examples 1 to 6, Comparative Examples 1 to 4) A resin composition obtained by uniformly mixing the components in the amounts shown in Table 1 with a super mixer was measured at a cylinder temperature of (C1: 14).
0 ° C, C2: 150 ° C, C3: 160 ° C, C4: 165
° C), adapter-temperature 160 ° C, die temperature 15
The mixture was fed to a 30 mm biaxial extruder set at 5 ° C. and cut with a pelletizer to obtain pellets. Next, the pellets were heated at a barrel temperature (B1: 150 ° C, B2: 160 ° C, B3: 170) using a 65 mm single extruder (L / D = 22, full flight screw, compression ratio = 3.0).
° C), and set the die temperature to (DH: 175 ° C,
(D1: 175 ° C., D2: 185 ° C.) to obtain a flat molded body.

【0024】表1に示す原材料は以下のものを使用し
た。 *1CPVC:徳山積水工業社製(原料PVC重合度8
00、塩素含有量64重量%) *2CPVC:徳山積水工業社製(原料PVC重合度8
00、塩素含有量66.5重量%) PVC:徳山積水工業社製TS−800E(重合度80
0) ケイ酸カルシウム:水澤化学社製 ケイ酸マグネシウム:水澤化学社製 オクチル錫メルカプト:三共有機合成社製 三塩基性硫酸鉛:堺化学社製 メチルメタクリレート樹脂:三菱レーヨン社製(品名P
−530A) アゾジカルボンアミド:永和化成社製(品名AC#1) 充填剤:白石工業社製(品名CCR) 滑剤:エステルワックス
The following raw materials were used as shown in Table 1. * 1 CPVC: manufactured by Tokuyama Sekisui Industry Co., Ltd. (raw material PVC polymerization degree 8
00, chlorine content 64% by weight) * 2 CPVC: manufactured by Tokuyama Sekisui Industry Co., Ltd. (raw material PVC polymerization degree 8
00, chlorine content 66.5% by weight) PVC: TS-800E manufactured by Tokuyama Sekisui Industry Co., Ltd. (polymerization degree 80
0) Calcium silicate: Magnesium silicate manufactured by Mizusawa Chemical Co., Ltd. Octyltin mercapto manufactured by Mizusawa Chemical Co., Ltd .: Tribasic lead sulfate manufactured by Sankyo Chemical Co., Ltd .: Methyl methacrylate resin manufactured by Sakai Chemical Co., Ltd .: manufactured by Mitsubishi Rayon Co., Ltd.
-530A) Azodicarbonamide: Eiwa Chemical Co., Ltd. (product name AC # 1) Filler: Shiraishi Industry Co., Ltd. (product name CCR) Lubricant: ester wax

【0025】(1)加熱変形温度 上記の樹脂組成物を組成物を200℃ロールにて3分間
混練後、200℃のプレスに予熱4分、加圧5分、面圧
75kg/cm2 にて厚さ6.4mmの板を作成し、J
IS K 7207に準拠して測定した。 (2)比重 得られた成形体をJIS K 7112 A法(水中置
換法)に準拠して測定した。 (3)セルの大きさ 上記(1)の成形体を液体窒素に入れ、衝撃を加えて切
断し、得られた断面に現れたセルの大きさを走査電子顕
微鏡にて測定した。 (4)表面性 上記(1)の成形体を目視にて観察し以下のようにラン
クをつけた。 ◎:表面が非常に良好 ○:良好 △:若干波打ち
×:大きく波打ちあり
(1) Heat deformation temperature The above resin composition was kneaded with a 200 ° C. roll for 3 minutes, and then preheated to a 200 ° C. press for 4 minutes, pressurized for 5 minutes, and surface pressure of 75 kg / cm 2 . Create a 6.4mm thick plate,
It was measured according to IS K 7207. (2) Specific Gravity The obtained molded body was measured in accordance with JIS K 7112 A method (substitution method in water). (3) Cell Size The molded article of (1) was placed in liquid nitrogen, cut by applying an impact, and the size of the cell that appeared on the obtained cross section was measured by a scanning electron microscope. (4) Surface properties The molded product of (1) was visually observed and ranked as follows. ◎: Very good surface ○: Good △: Slight wavy
×: Large undulation

【0026】[0026]

【表1】 [Table 1]

【0027】[0027]

【発明の効果】本発明のCPVC組成物は上述の如く構
成されており、安定剤として周期律表の第II族又は第
III族のケイ酸塩を用いることにより、鉛系安定剤に
匹敵する耐熱性が得られ、更にメタクリル酸エステルを
加えることにより発泡に適した溶融粘度が得られ、アゾ
ジカルボンアミド等の有機発泡剤を用いて発泡性、成形
性が良好なものとなる。
The CPVC composition of the present invention is constituted as described above, and is comparable to a lead-based stabilizer by using a silicate of Group II or Group III of the periodic table as a stabilizer. Heat resistance is obtained, and a melt viscosity suitable for foaming is obtained by further adding a methacrylic acid ester. Foamability and moldability are improved by using an organic foaming agent such as azodicarbonamide.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C08L 33:10) ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI C08L 33:10)

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 平均塩素含有量が60〜72重量%であ
る塩素化塩化ビニル樹脂単体または塩化ビニル樹脂との
混合物100重量部、周期律表第II族もしくは第II
I族金属のケイ酸塩、ケイ酸と前記金属の酸化物との複
合物、ケイ酸と前記金属の水酸化物との複合物、ケイ酸
と前記金属の炭酸塩との複合物、ハイドロタルサイト
類、又はゼオライト類のうち少なくとも1種以上の安定
剤0.5〜6重量部にメタクリル酸エステル系樹脂3〜
20重量部、分解型有機発泡剤0.1〜3重量部からな
ることを特徴とする発泡用塩素化塩化ビニル系樹脂組成
物。
1. A chlorinated vinyl chloride resin having an average chlorine content of 60 to 72% by weight or 100 parts by weight of a mixture with a vinyl chloride resin, Group II or II of the periodic table
Group I metal silicates, composites of silicic acid and said metal oxides, composites of silicic acid and said metal hydroxides, composites of silicic acid and said metal carbonates, hydrotals 0.5 to 6 parts by weight of at least one or more stabilizers among sites or zeolites are added to a methacrylate resin 3 to
A chlorinated vinyl chloride resin composition for foaming, comprising 20 parts by weight and 0.1 to 3 parts by weight of a decomposable organic foaming agent.
【請求項2】 前記周期律表第II族もしくは第III
族金属が、Mg、Al、Ca又はZnである請求項1記
載の発泡用塩素化塩化ビニル系樹脂組成物。
2. The group II or III of the periodic table
The chlorinated vinyl chloride resin composition for foaming according to claim 1, wherein the group metal is Mg, Al, Ca or Zn.
JP7562698A 1998-03-24 1998-03-24 Chlorinated vinyl chloride based resin composition for foaming Pending JPH11269295A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7562698A JPH11269295A (en) 1998-03-24 1998-03-24 Chlorinated vinyl chloride based resin composition for foaming

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7562698A JPH11269295A (en) 1998-03-24 1998-03-24 Chlorinated vinyl chloride based resin composition for foaming

Publications (1)

Publication Number Publication Date
JPH11269295A true JPH11269295A (en) 1999-10-05

Family

ID=13581640

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7562698A Pending JPH11269295A (en) 1998-03-24 1998-03-24 Chlorinated vinyl chloride based resin composition for foaming

Country Status (1)

Country Link
JP (1) JPH11269295A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001261873A (en) * 2000-03-21 2001-09-26 Kanegafuchi Chem Ind Co Ltd Foamable polyvinyl chloride-based resin composition
US20140336321A1 (en) * 2011-11-29 2014-11-13 Sekisui Chemical Co., Ltd. Chlorinated vinyl chloride resin composition for extrusion molding
JP2020164707A (en) * 2019-03-29 2020-10-08 株式会社カネカ Foamable chlorinated vinyl chloride-based resin particle, foamed particle thereof, and chlorinated vinyl chloride-based resin foam molded body using the same
CN115298252A (en) * 2020-03-24 2022-11-04 株式会社钟化 Expandable chlorinated vinyl chloride resin particles, expanded particles thereof, foamed molded article of chlorinated vinyl chloride resin using same, and method for producing expandable chlorinated vinyl chloride resin particles

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001261873A (en) * 2000-03-21 2001-09-26 Kanegafuchi Chem Ind Co Ltd Foamable polyvinyl chloride-based resin composition
US20140336321A1 (en) * 2011-11-29 2014-11-13 Sekisui Chemical Co., Ltd. Chlorinated vinyl chloride resin composition for extrusion molding
JP2020164707A (en) * 2019-03-29 2020-10-08 株式会社カネカ Foamable chlorinated vinyl chloride-based resin particle, foamed particle thereof, and chlorinated vinyl chloride-based resin foam molded body using the same
CN115298252A (en) * 2020-03-24 2022-11-04 株式会社钟化 Expandable chlorinated vinyl chloride resin particles, expanded particles thereof, foamed molded article of chlorinated vinyl chloride resin using same, and method for producing expandable chlorinated vinyl chloride resin particles
EP4130144A4 (en) * 2020-03-24 2024-04-17 Kaneka Corp Foamable chlorinated vinyl chloride-based resin particles, foamed particles thereof, chlorinated vinyl chloride-based resin foam molded article, and method for producing foamable chlorinated vinyl chloride resin particles

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