JPH08208923A - Polyvinyl chloride resin composition - Google Patents

Polyvinyl chloride resin composition

Info

Publication number
JPH08208923A
JPH08208923A JP7017129A JP1712995A JPH08208923A JP H08208923 A JPH08208923 A JP H08208923A JP 7017129 A JP7017129 A JP 7017129A JP 1712995 A JP1712995 A JP 1712995A JP H08208923 A JPH08208923 A JP H08208923A
Authority
JP
Japan
Prior art keywords
polyvinyl chloride
chloride resin
resin composition
parts
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP7017129A
Other languages
Japanese (ja)
Inventor
Shoji Ito
昌次 伊藤
Mikito Ishii
幹人 石井
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.)
Mitsubishi Plastics Inc
Original Assignee
Mitsubishi Plastics Inc
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 Mitsubishi Plastics Inc filed Critical Mitsubishi Plastics Inc
Priority to JP7017129A priority Critical patent/JPH08208923A/en
Publication of JPH08208923A publication Critical patent/JPH08208923A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE: To obtain a PVC composition excellent in moldability and capable of giving a molding of a good appearance. CONSTITUTION: This polyvinyl chloride resin composition is prepared by adding 0.5-3.0 pts.wt., per 100 pts.wt. polyvinyl chloride resin, calcium carbonate of a diameter of 0.05-0.10μm surface-coated with a fatty acid or its ester to a polyvinyl chloride resin composition containing an organotin stabilizer. This composition has good moldability and can give a molding of a good appearance.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は、成形加工性と得られる
成形品の外観が共に優れたポリ塩化ビニル樹脂組成物に
関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polyvinyl chloride resin composition which is excellent in both moldability and appearance of a molded product obtained.

【0002】[0002]

【従来の技術】ポリ塩化ビニル樹脂(以下PVCと略記
することがある)は、熱安定性に劣るため各種の熱安定
剤を添加して成形される。そのための安定剤としては、
鉛、カドミウム、バリウムなどの重金属を用いた安定剤
や、カルシウム、亜鉛、錫を用いた有機金属系安定剤が
用いられている。近年、前者の安定剤は食品衛生、労働
環境などの点から使用が制限される傾向にあり、後者の
安定剤を使用することが多くなってきた。後者の安定剤
のうち、カルシウムおよび亜鉛系の安定剤は熱安定性に
対する効果が低いので、主安定剤としては有機錫系の安
定剤が多用されている。
2. Description of the Related Art Polyvinyl chloride resin (hereinafter sometimes abbreviated as PVC) is inferior in thermal stability, so that it is molded by adding various thermal stabilizers. As a stabilizer for that,
Stabilizers that use heavy metals such as lead, cadmium, and barium, and organometallic stabilizers that use calcium, zinc, and tin are used. In recent years, the use of the former stabilizer tends to be restricted from the viewpoints of food hygiene, working environment, etc., and the latter stabilizer is often used. Among the latter stabilizers, calcium- and zinc-based stabilizers have a low effect on thermal stability, and thus organotin-based stabilizers are often used as the main stabilizers.

【0003】[0003]

【発明が解決しようとする課題】ところが有機錫系の安
定剤を使用した組成物は、成形装置の金属面(例えば口
金内面や押出機のバレル面やスクリユー面)への付着を
生じやすく、その結果、成形品に「すじ」が出たり、艶
が悪くなるなどの問題が生じる。またこの問題を配合で
解決しようとすると、成形加工性が悪化しやすい。
However, the composition using the organotin-based stabilizer is apt to adhere to the metal surface of the molding apparatus (for example, the inner surface of the die, the barrel surface of the extruder or the screw surface), and As a result, problems such as "streaking" appearing on the molded product and the gloss becoming poor occur. In addition, if this problem is solved by compounding, the moldability tends to deteriorate.

【0004】[0004]

【課題を解決するための手段】本発明者らは鋭意検討の
結果、成形加工性と得られる成形品の外観とを共に満足
させることができるポリ塩化ビニル系樹脂組成物を得る
ことに成功したものであり、その要旨は、有機錫系安定
剤を含有したポリ塩化ビニル樹脂組成物において、ポリ
塩化ビニル樹脂100重量部に対して、脂肪酸またはポ
リエステル(樹脂)で表面を被覆した平均粒径0.05
〜0.10μmの炭酸カルシウムを0.5〜3.0重量
部添加してなるポリ塩化ビニル樹脂組成物にある。
As a result of intensive studies, the present inventors have succeeded in obtaining a polyvinyl chloride resin composition capable of satisfying both moldability and appearance of the obtained molded product. In the polyvinyl chloride resin composition containing an organotin stabilizer, the gist is that the surface of the polyvinyl chloride resin is coated with a fatty acid or a polyester (resin), and the average particle size is 0. .05
The polyvinyl chloride resin composition is obtained by adding 0.5 to 3.0 parts by weight of calcium carbonate having a particle size of 0.10 μm.

【0005】以下、本発明を詳しく説明する。なお以下
の説明で添加割合を示す「部」はPVC100重量部に
対する「重量部」を意味する。本発明組成物のPVCと
しては、塩化ビニル単独重合体、または塩化ビニルに少
量、例えば1〜10重量%程度の共重合性モノマを共重
合した樹脂、あるいはこれらの樹脂を後塩素化した樹脂
を1種、または2種以上混合して使用することができ
る。共重合性モノマとしては例えばエチレン、プロピレ
ン、イソブテン、酢酸ビニル、フツ化ビニル、塩化ビニ
リデン、スチレン、アクリル酸、アクリル酸アルキルエ
ステルなどが挙げられる。
The present invention will be described in detail below. In addition, in the following description, "part" indicating the addition ratio means "part by weight" relative to 100 parts by weight of PVC. As the PVC of the composition of the present invention, a vinyl chloride homopolymer, a resin obtained by copolymerizing vinyl chloride with a small amount, for example, about 1 to 10% by weight of a copolymerizable monomer, or a resin obtained by post-chlorinating these resins is used. One kind or a mixture of two or more kinds can be used. Examples of the copolymerizable monomer include ethylene, propylene, isobutene, vinyl acetate, vinyl fluoride, vinylidene chloride, styrene, acrylic acid, and alkyl acrylate.

【0006】これらのPVCの重合度は得ようとする成
形品の種類にもより異なるが、600〜2,000程度
のもの、特に700〜1,500程度のものが好適に使
用でき、重合法も懸濁重合、乳化重合あるいは塊状重合
によるものをいずれも使用することができる。
The degree of polymerization of these PVCs varies depending on the type of molded product to be obtained, but those of about 600 to 2,000, particularly 700 to 1,500 can be preferably used, and the polymerization method Also, suspension polymerization, emulsion polymerization or bulk polymerization can be used.

【0007】このPVCに添加する有機錫系安定剤とし
ては、従来から知られた各種のものを特に制限なく使用
することができるが、ジブチル錫マレート、ジオクチル
錫マレートなどのアルキル錫マレートあるいはそのポリ
マ:ジブチル錫ラウレート、ジオクチル錫ラウレートな
どのアルキル錫ラウレート:ジメチル錫ジドデシルメル
カプト、ジブチル錫ジドデシルメルカプト、ジフエニル
錫ジドデシルメルカプトなどのアルキル錫アルキルメル
カプト:ジブチル錫ジフエニルメルカプトなどのアルキ
ル錫アリールメルカプト:ジブチル錫ジイソオクチルチ
オグリコレート、ジオクチル錫ジイソオクチルチオグリ
コレート、ジブチル錫ジn−オクタデシルチオグリコレ
ート、ジブチル錫β−メルカプトプロピオネートなどの
錫メルカプト酸エステル:などを例示することができ
る。有機錫系安定剤の添加量は、組成物に十分な熱安定
性を付与できる量であればよく、一般には0.2〜3
部、好適には0.3〜1.0部の範囲である。この有機
錫系安定剤には、補助安定剤としてエポキシ化大豆油、
エポキシ化アマニ油などのエポキシ化合物や、トリアル
キルホスフアイト、アルキルアリールホスフアイトなど
のホスフアイト化合物を併用することもできる。
As the organotin stabilizer to be added to this PVC, various conventionally known ones can be used without particular limitation, but alkyltin malates such as dibutyltin malate and dioctyltin malate or polymers thereof are usable. : Alkyl tin laurate such as dibutyl tin laurate and dioctyl tin laurate: Alkyl tin alkyl mercapto such as dimethyl tin didodecyl mercapto, dibutyl tin didodecyl mercapto, diphenyl tin didodecyl mercapto: Alkyl tin aryl mercapto such as dibutyl tin diphenyl mercapto: Tin mercapto acid salts such as dibutyl tin diisooctyl thioglycolate, dioctyl tin diisooctyl thioglycolate, dibutyl tin di n-octadecyl thioglycolate, dibutyl tin β-mercapto propionate Tel: and the like can be exemplified. The addition amount of the organotin stabilizer may be an amount that can impart sufficient thermal stability to the composition, and is generally 0.2 to 3
Parts, preferably 0.3 to 1.0 parts. This organotin stabilizer includes epoxidized soybean oil as a co-stabilizer,
Epoxy compounds such as epoxidized linseed oil and phosphite compounds such as trialkyl phosphite and alkylaryl phosphite can also be used in combination.

【0008】本発明組成物の特徴である炭酸カルシウム
は、脂肪酸または脂肪酸エステルで表面を被覆した平均
粒径0.05〜0.10μmの粒子である。表面を被覆
しない炭酸カルシウムまたは平均粒径の大きすぎる炭酸
カルシウムでは、少量の添加でも成形加工性を損なう。
また炭酸カルシウム以外の、例えばケイ酸アルミニウム
などの微粒子は、多量に添加すれば成形加工性は問題な
いものの、微粒子が凝集してブツになりやすく、衝撃強
度などの機械的強度も低下する。
Calcium carbonate, which is a feature of the composition of the present invention, is a particle having an average particle size of 0.05 to 0.10 μm, the surface of which is coated with a fatty acid or a fatty acid ester. With calcium carbonate that does not cover the surface or calcium carbonate with an average particle size that is too large, even if added in a small amount, the moldability is impaired.
Further, if fine particles other than calcium carbonate, such as aluminum silicate, are added in a large amount, there is no problem in molding processability, but the fine particles tend to agglomerate to form lumps, and mechanical strength such as impact strength also decreases.

【0009】炭酸カルシウム粒子表面を被覆する脂肪酸
またはエステルとしては、ステアリン酸、パルミチン
酸、または、ポリグリセリンとこれら脂肪酸とのエステ
ルを挙げることができる。
Examples of the fatty acid or ester coating the surface of the calcium carbonate particles include stearic acid, palmitic acid, or esters of polyglycerin with these fatty acids.

【0010】炭酸カルシウムの添加量は0.5〜3.0
部の範囲であり、0.5部未満では外観改良効果がな
く、3.0部を越えると成形加工性が悪化する。好適範
囲は1.0〜2.5部である。
The amount of calcium carbonate added is 0.5 to 3.0.
If it is less than 0.5 part, there is no effect of improving the appearance, and if it exceeds 3.0 parts, the moldability is deteriorated. The preferred range is 1.0 to 2.5 parts.

【0011】本発明組成物には、上記成分以外に各種の
添加剤を併用することができる。例えば、ABS樹脂、
MBS樹脂、塩素化ポリエチレン、ブチルアクリレート
を主体とするアクリルゴム系などの耐衝撃性改良剤;パ
ラフインワツクス、マイクロクリスタリンワツクス、ポ
リエチレンワツクスなどのワツクス類、オクチルアルコ
ール、デシルアルコール、ラウリルアルコール、ステア
リルアルコールなどの脂肪族アルコール;ステアリン酸
カルシウム、ステアリン酸亜鉛などの金属石鹸類;n−
ブチルステアレートなどの脂肪酸エステルなどの滑剤;
サリチル酸エステル系、ベンゾフエノン系、ベンゾトリ
アゾール系などの紫外線吸収剤;などを使用することが
でき、少量のシリカ、酸化チタン、タルク、クレー、カ
オリン、マイカなどの無機質充填剤を併用したり、その
他着色剤、難燃剤、帯電防止剤などを添加することがで
きる。
The composition of the present invention may contain various additives in addition to the above components. For example, ABS resin,
Impact resistance improvers such as MBS resin, chlorinated polyethylene, acrylic rubber based mainly on butyl acrylate; waxes such as paraffin wax, microcrystalline wax, polyethylene wax, octyl alcohol, decyl alcohol, lauryl alcohol, Aliphatic alcohols such as stearyl alcohol; metal soaps such as calcium stearate and zinc stearate; n-
Lubricants such as fatty acid esters such as butyl stearate;
UV absorbers such as salicylate, benzophenone, benzotriazole, etc. can be used, and a small amount of silica, titanium oxide, talc, clay, kaolin, mica and other inorganic fillers can also be used, and other coloring Agents, flame retardants, antistatic agents and the like can be added.

【0012】また本発明組成物には、ジn−オクチルフ
タレート、ジ−(2−エチルヘキシル)フタレート、ジ
イソデシルフタレートなどのフタル酸エステルや、ジイ
ソブチルアジペート、ジ−(2−エチルヘキシル)アジ
ペート、ジイソデシルアジペートなどのアジピン酸エス
テルなどの常用の可塑剤を用いることができるが、本発
明は流動性の悪い無可塑ないし可塑剤添加量がPVC1
00部に対し10部以下であるような、硬質ないし半硬
質組成物として特に効果が高く、特に可塑剤を実質上含
まない無可塑組成物として好適である。
In the composition of the present invention, phthalic acid esters such as di-n-octyl phthalate, di- (2-ethylhexyl) phthalate and diisodecyl phthalate, diisobutyl adipate, di- (2-ethylhexyl) adipate, diisodecyl adipate, etc. Although a conventional plasticizer such as adipic acid ester can be used, in the present invention, the plasticizer having poor fluidity or the plasticizer added is PVC1.
It is particularly effective as a hard or semi-hard composition having a content of 10 parts or less with respect to 00 parts, and is particularly suitable as a non-plastic composition substantially containing no plasticizer.

【0013】本発明組成物は、特に溶融押出成形用に好
適であり、単軸スクリユー押出機、二軸スクリユー押出
機などによりシート、板、パイプ、異型押出品など各種
の成形品を得ることができる。特に得られる成形品が高
い機械的強度を維持するので、引張強度や耐衝撃強度を
必要とする用途に、また本来成形加工性の悪い硬質配合
として好適なものである。
The composition of the present invention is particularly suitable for melt extrusion molding, and various molded products such as sheets, plates, pipes and profile extruded products can be obtained by a single screw extruder, a twin screw extruder or the like. it can. In particular, since the obtained molded article maintains high mechanical strength, it is suitable for applications requiring tensile strength and impact resistance, and as a hard compound which originally has poor moldability.

【0014】[0014]

【実施例】以下、実施例により本発明を具体的に説明す
る。 (実施例)以下に示す組成物をヘンシエルミキサで混合
した後、65mmφ単軸スクリユー押出機により厚さ2
mmの平板を押出成形した。押出温度条件は、押出機の
バレル温度を140〜200℃の範囲、口金温度を16
0〜190℃の範囲とし、各組成物に応じた最適条件を
設定して行った。
The present invention will be described below in detail with reference to examples. (Example) The following compositions were mixed with a Henschel mixer, and then a thickness of 2 mm was obtained with a 65 mmφ single-screw extruder.
A mm flat plate was extruded. The extrusion temperature conditions are as follows: the barrel temperature of the extruder is in the range of 140 to 200 ° C., and the die temperature is 16.
The temperature was set in the range of 0 to 190 ° C., and optimum conditions were set according to each composition.

【0015】 PVC(単独重合体、平均重合度1300) 100部 オクチル錫メルカプト 0.7 MBS衝撃改良剤 5 ポリエチレンワツクス 0.5 炭酸カルシウム 0.5〜3.0 この炭酸カルシウムは、表面をステアリン酸で被覆した
平均粒径0.08μmのものである。
PVC (homopolymer, average degree of polymerization 1300) 100 parts Octyl tin mercapto 0.7 MBS impact modifier 5 Polyethylene wax 0.5 Calcium carbonate 0.5 to 3.0 This calcium carbonate stearinizes the surface. It has an average particle diameter of 0.08 μm coated with an acid.

【0016】その結果、炭酸カルシウム0.5部では成
形加工性は良好だが外観がやや悪く、3.0部では外観
が良好だが成形加工性はやや劣り、1.0〜2.5部の
範囲では両者とも良好であった。
As a result, when 0.5 part of calcium carbonate has a good moldability, the appearance is a little bad, and when 3.0 part is calcium carbonate, the appearance is good but the moldability is a little poor, and the range is 1.0 to 2.5 parts. So both were good.

【0017】(比較例)実施例の炭酸カルシウムに代え
て、表面被覆しない平均粒径1.25μmの炭酸カルシ
ウム、または平均粒径2μmのケイ酸アルミニウムを添
加して、実施例1と同様の試験を行った。
(Comparative Example) The same test as in Example 1 was conducted by adding calcium carbonate having an average particle size of 1.25 μm or aluminum silicate having an average particle size of 2 μm, which was not surface-coated, in place of the calcium carbonate of Example. I went.

【0018】その結果、この炭酸カルシウムは0.5部
添加ですでに成形加工性が悪かった。また、ケイ酸アル
ミニウムは0.5部添加では成形加工性はよいものの外
観は改良されず、また外観がやや改良される量である
1.5部では成形加工性が悪かった。
As a result, the formability of this calcium carbonate was already poor when 0.5 part was added. When 0.5 part of aluminum silicate was added, the moldability was good, but the appearance was not improved, and the moldability was poor at 1.5 parts, which is a slightly improved appearance.

【0019】[0019]

【発明の効果】本発明によれば、有機錫系安定剤を使用
したPVC組成物に特定の炭酸カルシウム粒子を添加す
ることにより、成形加工性と得られる成形品の外観が共
に優れた組成物が得られる。
EFFECTS OF THE INVENTION According to the present invention, by adding specific calcium carbonate particles to a PVC composition containing an organotin stabilizer, the composition has excellent moldability and appearance of the resulting molded article. Is obtained.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 有機錫系安定剤を含有したポリ塩化ビニ
ル樹脂組成物において、ポリ塩化ビニル樹脂100重量
部に対して、脂肪酸または脂肪酸エステルで表面を被覆
した平均粒径0.05〜0.10μmの炭酸カルシウム
を0.5〜3.0重量部添加してなるポリ塩化ビニル樹
脂組成物。
1. A polyvinyl chloride resin composition containing an organic tin-based stabilizer, wherein the surface of the polyvinyl chloride resin is coated with a fatty acid or a fatty acid ester with respect to 100 parts by weight of the polyvinyl chloride resin. A polyvinyl chloride resin composition obtained by adding 0.5 to 3.0 parts by weight of 10 μm calcium carbonate.
【請求項2】 ポリ塩化ビニル樹脂組成物が、可塑剤添
加量がポリ塩化ビニル樹脂100重量部に対し10重量
部以下である硬質ないし半硬質組成物であることを特徴
とする請求項1記載のポリ塩化ビニル樹脂組成物。
2. The polyvinyl chloride resin composition is a hard or semi-hard composition in which the amount of plasticizer added is 10 parts by weight or less based on 100 parts by weight of the polyvinyl chloride resin. Polyvinyl chloride resin composition.
【請求項3】 炭酸カルシウムの表面を被覆する脂肪酸
または脂肪酸エステルが、ステアリン酸、パルミチン
酸、または、ポリグリセリンとこれら脂肪酸とのエステ
ルである請求項1または2記載のポリ塩化ビニル樹脂組
成物。
3. The polyvinyl chloride resin composition according to claim 1, wherein the fatty acid or fatty acid ester coating the surface of calcium carbonate is stearic acid, palmitic acid, or an ester of polyglycerin and these fatty acids.
【請求項4】 有機錫系安定剤が錫メルカプト系安定剤
であり、その含有量がポリ塩化ビニル樹脂100重量部
に対し0.2〜3重量部、好適には0.3〜1.0重量
部の範囲である請求項1、2または3記載のポリ塩化ビ
ニル樹脂組成物。
4. The organotin stabilizer is a tin mercapto stabilizer, and the content thereof is 0.2 to 3 parts by weight, preferably 0.3 to 1.0, based on 100 parts by weight of the polyvinyl chloride resin. The polyvinyl chloride resin composition according to claim 1, 2 or 3 in the range of parts by weight.
JP7017129A 1995-02-03 1995-02-03 Polyvinyl chloride resin composition Pending JPH08208923A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7017129A JPH08208923A (en) 1995-02-03 1995-02-03 Polyvinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7017129A JPH08208923A (en) 1995-02-03 1995-02-03 Polyvinyl chloride resin composition

Publications (1)

Publication Number Publication Date
JPH08208923A true JPH08208923A (en) 1996-08-13

Family

ID=11935432

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7017129A Pending JPH08208923A (en) 1995-02-03 1995-02-03 Polyvinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPH08208923A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112210123A (en) * 2020-10-22 2021-01-12 云南锡业集团(控股)有限责任公司研发中心 Preparation method of low-cost coated flame-retardant smoke suppressant

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4815457B1 (en) * 1969-05-29 1973-05-15
JPS5112849A (en) * 1974-04-24 1976-01-31 Hitachi Chemical Co Ltd KOSHITSUEN KABINIRUJUSHISOSEIBUTSU
JPS5134940A (en) * 1974-09-20 1976-03-25 Showa Electric Wire & Cable Co TEIENGAINANNENSEIENKABINIRUJUSHISOSEIBUTSU
JPS5249254A (en) * 1975-10-18 1977-04-20 Hiroshi Takahashi Novel iorganic filler
JPS53134850A (en) * 1977-04-29 1978-11-24 Gaf Corp White poly*vinyl chloride* composition
JPS5543144A (en) * 1978-09-23 1980-03-26 Matsushita Electric Works Ltd Moding material of vinyl chloride resin
JPS55106256A (en) * 1979-02-08 1980-08-14 Tokuyama Soda Co Ltd Polyvinyl chloride composition
JPS5827734A (en) * 1981-08-12 1983-02-18 Adeka Argus Chem Co Ltd Polyvinyl chloride resin composition
JPH04216845A (en) * 1990-12-18 1992-08-06 Asahi Denka Kogyo Kk Vinyl chloride resin composition
JPH06288867A (en) * 1993-04-01 1994-10-18 Shin Etsu Polymer Co Ltd Rigid polyvinyl chloride-based pipe and its evaluation method
JPH07300545A (en) * 1994-03-08 1995-11-14 Sekisui Chem Co Ltd Vinyl chloride resin composition
JPH0881605A (en) * 1994-09-14 1996-03-26 Chisso Corp Rigid vinyl chloride-based resin composition for calendering

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4815457B1 (en) * 1969-05-29 1973-05-15
JPS5112849A (en) * 1974-04-24 1976-01-31 Hitachi Chemical Co Ltd KOSHITSUEN KABINIRUJUSHISOSEIBUTSU
JPS5134940A (en) * 1974-09-20 1976-03-25 Showa Electric Wire & Cable Co TEIENGAINANNENSEIENKABINIRUJUSHISOSEIBUTSU
JPS5249254A (en) * 1975-10-18 1977-04-20 Hiroshi Takahashi Novel iorganic filler
JPS53134850A (en) * 1977-04-29 1978-11-24 Gaf Corp White poly*vinyl chloride* composition
JPS5543144A (en) * 1978-09-23 1980-03-26 Matsushita Electric Works Ltd Moding material of vinyl chloride resin
JPS55106256A (en) * 1979-02-08 1980-08-14 Tokuyama Soda Co Ltd Polyvinyl chloride composition
JPS5827734A (en) * 1981-08-12 1983-02-18 Adeka Argus Chem Co Ltd Polyvinyl chloride resin composition
JPH04216845A (en) * 1990-12-18 1992-08-06 Asahi Denka Kogyo Kk Vinyl chloride resin composition
JPH06288867A (en) * 1993-04-01 1994-10-18 Shin Etsu Polymer Co Ltd Rigid polyvinyl chloride-based pipe and its evaluation method
JPH07300545A (en) * 1994-03-08 1995-11-14 Sekisui Chem Co Ltd Vinyl chloride resin composition
JPH0881605A (en) * 1994-09-14 1996-03-26 Chisso Corp Rigid vinyl chloride-based resin composition for calendering

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112210123A (en) * 2020-10-22 2021-01-12 云南锡业集团(控股)有限责任公司研发中心 Preparation method of low-cost coated flame-retardant smoke suppressant

Similar Documents

Publication Publication Date Title
JP6327471B2 (en) Wire covering material and covered wire
JP6315207B2 (en) Soft vinyl chloride resin composition, molded body, wire coating material and coated wire
EP0492803B1 (en) Stabilized halogen containing polymer compositions
TWI428348B (en) Stabilized polymer compositions
EP2298835B1 (en) Stabilized polymer compositions
US5270366A (en) Lead stabilized, flexible polymeric blends containing polyvinylchloride
JPH04233910A (en) Improved barrier pvc resin, compound, and article derived therefrom
JP6082750B2 (en) Stabilized composition of halogenated polymer
JPS6210257B2 (en)
JPH08208923A (en) Polyvinyl chloride resin composition
US3654211A (en) Alkylene bis-dialkyl aromatic tricarboxylate plasticizers
JP2003292712A (en) Chlorinated vinyl chloride-based resin composition and extrusion-molded product therefrom
JPH08208924A (en) Polyvinyl chloride resin composition
JPH1129676A (en) Vinyl chloride-based resin composition
JP2842732B2 (en) Vinyl chloride resin composition
US20200010638A1 (en) Halogen containing polymer composition with tin stabilizer and co-stabilizer
JPH0881605A (en) Rigid vinyl chloride-based resin composition for calendering
US3682924A (en) Readily processable, rigid vinyl chloride polymer compositions containing chlorinated olefin polymer wax
JPH07300545A (en) Vinyl chloride resin composition
JP3223023B2 (en) Soft vinyl chloride resin composition and soft vinyl chloride resin film
US3567681A (en) Stabilizer compositions for halogenated resins,employing the metal salts of neoacids
US4972012A (en) Polyvinyl chloride resin composition
JP3311532B2 (en) Extrusion molding resin composition
US20100056683A1 (en) Mixtures of n-alkanols and their use
JP2001207003A (en) Vinyl chloride-based resin composition and outdoor building material using the same

Legal Events

Date Code Title Description
A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20031224