JPH08295773A - Vinyl chloride resin composition - Google Patents
Vinyl chloride resin compositionInfo
- Publication number
- JPH08295773A JPH08295773A JP10377095A JP10377095A JPH08295773A JP H08295773 A JPH08295773 A JP H08295773A JP 10377095 A JP10377095 A JP 10377095A JP 10377095 A JP10377095 A JP 10377095A JP H08295773 A JPH08295773 A JP H08295773A
- Authority
- JP
- Japan
- Prior art keywords
- vinyl chloride
- chloride resin
- resin composition
- vinyl
- composition
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、塩化ビニル系樹脂組成
物に関する。TECHNICAL FIELD The present invention relates to a vinyl chloride resin composition.
【0002】[0002]
【従来の技術】従来より塩化ビニル樹脂は、機械的強
度、難燃性、耐候性、耐薬品性等に優れているため、各
種の成形品として広範囲に利用されているが、その反
面、加熱成形加工を行う際に、脱塩化水素を主とする加
熱分解を起こすという欠点を有している。このため、成
形体の機械的性質の低下や色調の悪化等が生じて、商品
価値の低下を招くという問題点があった。2. Description of the Related Art Conventionally, vinyl chloride resins have been widely used as various molded products because of their excellent mechanical strength, flame retardancy, weather resistance, chemical resistance, etc. It has a drawback that when it is molded, it undergoes thermal decomposition mainly due to dehydrochlorination. Therefore, there has been a problem that the mechanical properties of the molded product are deteriorated, the color tone is deteriorated, and the commercial value is decreased.
【0003】このような問題点を改善するために、従来
より種々の安定剤を、単独もしくは二種以上組み合わせ
て使用することが提案されている。このような安定剤と
しては、各種の金属石鹸類、有機錫化合物、鉛化合物、
有機亜燐酸塩等が挙げられ、例えば、特開昭63−26
8756号公報には、有機錫化合物と過塩素酸を併用す
ることにより、成形体の透明性を阻害することなく、熱
安定性を向上させる方法が開示されている。In order to improve such problems, it has been proposed to use various stabilizers individually or in combination of two or more kinds. As such a stabilizer, various metal soaps, organotin compounds, lead compounds,
Examples of the organic phosphite include, for example, JP-A-63-26
Japanese Patent No. 8756 discloses a method of improving thermal stability by using an organic tin compound and perchloric acid together without impairing the transparency of a molded article.
【0004】また、有機錫化合物とステアリン酸カルシ
ウム、あるいはエポキシ化大豆油等の塩化水素捕捉剤を
併用すると、成形時の熱安定性が向上することが知られ
ている。しかしながら、有機錫化合物は、成形時の熱安
定性に優れている反面、多量に添加したり、エポキシ化
大豆油のような塩化水素捕捉剤を併用すると、成形体の
耐熱性を大きく低下させるという問題点があった。It is also known that when an organic tin compound is used in combination with calcium stearate or a hydrogen chloride scavenger such as epoxidized soybean oil, the thermal stability during molding is improved. However, while the organic tin compound is excellent in thermal stability during molding, when added in a large amount or in combination with a hydrogen chloride scavenger such as epoxidized soybean oil, the heat resistance of the molded article is significantly reduced. There was a problem.
【0005】[0005]
【発明が解決しようとする課題】本発明は、上記欠点に
鑑みてなされたものであり、その目的は、成形加工時の
熱安定性に優れ、かつ耐熱性に優れた成形体の得られる
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 The present invention has been made in view of the above-mentioned drawbacks, and an object thereof is to obtain a molded product having excellent heat stability during molding and heat resistance. It is to provide a vinyl resin composition.
【0006】[0006]
【課題を解決するための手段】本発明の塩化ビニル系樹
脂組成物は、塩化ビニル系樹脂及び炭酸ナトリウムから
なる。The vinyl chloride resin composition of the present invention comprises a vinyl chloride resin and sodium carbonate.
【0007】上記塩化ビニル系樹脂としては、従来から
知られているものを使用することができ、例えば、塩
化ビニルの単独重合体、塩化ビニルモノマーと塩化ビ
ニル以外の重合性単量体との共重合体、塩化ビニル以
外の重合体に塩化ビニルをグラフトさせたグラフト共重
合体、これらの(共)重合体を従来公知の方法で後塩
素化して得られた塩素化塩化ビニル系樹脂、前記
(共)重合体と塩素化塩化ビニル系樹脂との混合物等が
挙げられる。As the vinyl chloride resin, those conventionally known can be used. For example, a homopolymer of vinyl chloride, a copolymer of vinyl chloride monomer and a polymerizable monomer other than vinyl chloride can be used. Polymers, graft copolymers obtained by grafting vinyl chloride onto polymers other than vinyl chloride, chlorinated vinyl chloride resins obtained by post-chlorination of these (co) polymers by a conventionally known method, the above ( Examples thereof include a mixture of a co) polymer and a chlorinated vinyl chloride resin.
【0008】上記塩化ビニル以外の重合性単量体として
は、反応性二重結合を有するものであれば特に限定され
ず、例えば、エチレン、プロピレン、ブチレン等のα−
オレフィン類;酢酸ビニル、プロピオン酸ビニル等のビ
ニルエステル類;イソブチルビニルエーテル、セチルビ
ニルエーテル、フェニルビニルエーテル等のビニルエー
テル類;メチルアクリレート、エチルアクリレート等の
アクリル酸エステル類;メチルメタクリレート、エチル
メタクリレート等のメタクリル酸エステル類;スチレ
ン、α−メチルスチレン等の芳香族ビニル類;アクリロ
ニトリル、メタアクリロニトリル等のシアン化ビニル
類;塩化ビニリデン、ふっ化ビニル等のハロゲン化ビニ
ル類;マレイン酸ジメチル、フマル酸ジメチル等の不飽
和ジカルボン酸エステル類;無水マレイン酸等の不飽和
ジカルボン酸無水物、N−フェニルマレイミド、N−シ
クロヘキシルマレイミド等のN−置換マレイミド類など
が挙げら、これらは単独で用いられてもよく、二種以上
が併用されてもよい。The polymerizable monomer other than vinyl chloride is not particularly limited as long as it has a reactive double bond, and for example, α-, such as ethylene, propylene and butylene.
Olefins; Vinyl acetates such as vinyl acetate and vinyl propionate; Vinyl ethers such as isobutyl vinyl ether, cetyl vinyl ether and phenyl vinyl ether; Acrylic esters such as methyl acrylate and ethyl acrylate; Methacrylic acid esters such as methyl methacrylate and ethyl methacrylate Kinds: Aromatic vinyls such as styrene and α-methylstyrene; Vinyl cyanides such as acrylonitrile and methacrylonitrile; Vinyl halides such as vinylidene chloride and vinyl fluoride; Unsaturation such as dimethyl maleate and dimethyl fumarate Dicarboxylic acid esters; unsaturated dicarboxylic acid anhydrides such as maleic anhydride; N-substituted maleimides such as N-phenylmaleimide and N-cyclohexylmaleimide; May be used in, two or more of them may be used in combination.
【0009】上記グラフト共重合体に使用される上記塩
化ビニル以外の重合体としては、特に限定されず、例え
ば、(メタ)アクリル酸エステル重合体、エチレン−酢
酸ビニル共重合体、エチレン−アクリル酸エステル共重
合体、塩素化ポリエチレン、クロルスルホン化ポリエチ
レン、ポリウレタン等が挙げられる。The polymer other than vinyl chloride used in the graft copolymer is not particularly limited, and examples thereof include (meth) acrylic acid ester polymers, ethylene-vinyl acetate copolymers, ethylene-acrylic acid. Examples thereof include ester copolymers, chlorinated polyethylene, chlorosulfonated polyethylene and polyurethane.
【0010】上記塩化ビニル系樹脂の平均重合度は、小
さくなると得られる成形体の機械的物性が不足し、大き
くなると成形時の溶融粘度が高くなって成形が困難にな
るので、400〜1,400が好ましい。When the average degree of polymerization of the above vinyl chloride resin is small, the mechanical properties of the obtained molded product are insufficient, and when it is large, the melt viscosity at the time of molding becomes high and molding becomes difficult. 400 is preferred.
【0011】上記塩素化塩化ビニル系樹脂の塩素化度
は、大きくなると成形性が著しく低下するので、57
(塩化ビニル樹脂の塩素化度)〜72重量%が好まし
く、より好ましくは、57〜68重量%である。If the degree of chlorination of the above chlorinated vinyl chloride resin increases, the moldability remarkably decreases.
The degree of chlorination of the vinyl chloride resin is preferably 72 to 72% by weight, more preferably 57 to 68% by weight.
【0012】本発明の塩化ビニル系樹脂組成物におい
て、炭酸ナトリウムの添加量は、少なくなると十分な熱
安定効果が得られず、多くなると成形性が著しく低下す
ると共に耐衝撃性も低下するので、塩化ビニル系樹脂1
00重量部に対して、0.1〜30重量部に限定され、
好ましくは0.3〜20重量部である。In the vinyl chloride resin composition of the present invention, when the amount of sodium carbonate added is small, a sufficient heat stabilizing effect cannot be obtained, and when it is large, the moldability is remarkably lowered and the impact resistance is also lowered. Vinyl chloride resin 1
It is limited to 0.1 to 30 parts by weight with respect to 00 parts by weight,
It is preferably 0.3 to 20 parts by weight.
【0013】上記塩化ビニル系樹脂組成物には、必要に
応じて、安定剤、滑剤、加工助剤、酸化防止剤、紫外線
吸収剤、発泡剤等が添加されてもよい。If necessary, stabilizers, lubricants, processing aids, antioxidants, ultraviolet absorbers, foaming agents and the like may be added to the vinyl chloride resin composition.
【0014】上記製造工程において各成分の混合に使用
される装置としては、一般に公知の混合装置が使用可能
であり、例えば、ヘンシェルミキサー、擂潰機、リボン
ブレンダー等が挙げられる。As a device used for mixing the respective components in the above manufacturing process, a generally known mixing device can be used, and examples thereof include a Henschel mixer, a crusher, a ribbon blender and the like.
【0015】上記塩化ビニル系樹脂組成物の成形方法と
しては、従来公知の成形方法が採用可能であり、例え
ば、押出成形法、射出成形法、カレンダー成形法等が挙
げられる。上記成形方法により、例えば、パイプ、継
手、プレート、デッキ材等を得ることができる。As a molding method of the vinyl chloride resin composition, a conventionally known molding method can be adopted, and examples thereof include an extrusion molding method, an injection molding method and a calender molding method. By the above-mentioned molding method, for example, pipes, joints, plates, deck materials, etc. can be obtained.
【0016】[0016]
【実施例】以下、本発明の実施例を説明する。 (実施例1〜5、比較例1〜3)表1及び2に示した所
定量の、塩化ビニル樹脂(徳山積水社製「TS1000
R」、重合度:1,000)、ジオクチル錫メルカプト
(三共有機合成社製「ONZ−142F」、有機錫系安
定剤)、滑剤としてモノグリセリンステアレート(理研
ビタミン社製「リケマールS−100」)及びポリエチ
レンワックス(三井石油化学社製「ハイワックス220
MP」)を、ヘンシェルミキサーに供給して5分間混合
し、塩化ビニル系樹脂組成物を得た。Embodiments of the present invention will be described below. (Examples 1 to 5 and Comparative Examples 1 to 3) A predetermined amount of vinyl chloride resin shown in Tables 1 and 2 ("TS1000 manufactured by Tokuyama Sekisui Co., Ltd."
R ”, degree of polymerization: 1,000), dioctyl tin mercapto (“ ONZ-142F ”manufactured by Sansha Machine Synthesis Co., organotin stabilizer), monoglycerin stearate as a lubricant (“ Rikemar S-100 ”manufactured by Riken Vitamin Co., Ltd. ") And polyethylene wax (Mitsui Petrochemical's" High Wax 220 "
MP ") was supplied to a Henschel mixer and mixed for 5 minutes to obtain a vinyl chloride resin composition.
【0017】この塩化ビニル系樹脂組成物につき、次の
評価を行い、その結果を表1及び2に示した。 (1)耐熱性 この樹脂組成物を、8インチミキシングロールにて19
0℃で巻き付き後、3分間混練して、1mm厚のシート
を得た後、このシートを30×30mmに切断して試験
片を作製した。この試験片を100℃のギヤオーブンで
加熱して10分間隔で取り出し、熱安定性として分解す
るまでの時間〔試験片が明らかに黒色を帯びるか、黒い
斑点を発生し始める時間(分)〕を目視観察により測定
した。 (2)ビカット軟化温度 上記1mm厚のシートを190℃で3分間予熱した後、
圧力150kg/cm 2 で2分間プレス成形して1mm
厚のプレートを作製した。このプレートから切断した試
験片を使用し、耐熱性の指標としてJIS K7206
(荷重1kgf)に準拠して、ビカット軟化温度を測定
した。 (3)シャルピー衝撃値 (2)で得られたプレートから試験片を作製し、耐衝撃
性の指標としてJISK7111に準拠して、シャルピ
ー衝撃値を測定した。Regarding this vinyl chloride resin composition,
The evaluation was performed, and the results are shown in Tables 1 and 2. (1) Heat resistance This resin composition was applied on an 8-inch mixing roll for 19 hours.
After wrapping at 0 ° C, kneading for 3 minutes, 1mm thick sheet
After obtaining this, cut this sheet into 30 x 30 mm and test
Pieces were made. This test piece is placed in a gear oven at 100 ° C
It is heated and taken out at intervals of 10 minutes and decomposed as heat stability.
Time to reach the test piece (clearly black or black
The time (minutes) at which the spots start to occur] is measured by visual observation.
did. (2) Vicat softening temperature After preheating the 1 mm thick sheet at 190 ° C. for 3 minutes,
Pressure 150kg / cm 21 mm after press molding for 2 minutes
A thick plate was made. Trials cut from this plate
JIS K7206 is used as an index of heat resistance by using a test piece.
Vicat softening temperature is measured according to (load 1 kgf)
did. (3) Charpy impact value A test piece was prepared from the plate obtained in (2) and the impact resistance
In accordance with JIS K7111 as a sex index, Charpy
-The impact value was measured.
【0018】[0018]
【表1】 [Table 1]
【0019】[0019]
【表2】 [Table 2]
【0020】[0020]
【発明の効果】本発明の塩化ビニル系樹脂組成物の構成
は、上述の通りであり、成形加工時の熱安定性に優れ、
かつ得られた成形体は耐熱性に優れる。The constitution of the vinyl chloride resin composition of the present invention is as described above, and it has excellent thermal stability during molding.
Moreover, the obtained molded product has excellent heat resistance.
Claims (1)
トリウム0.1〜30重量部からなることを特徴とする
塩化ビニル系樹脂組成物。1. A vinyl chloride resin composition comprising 100 parts by weight of a vinyl chloride resin and 0.1 to 30 parts by weight of sodium carbonate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10377095A JPH08295773A (en) | 1995-04-27 | 1995-04-27 | Vinyl chloride resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10377095A JPH08295773A (en) | 1995-04-27 | 1995-04-27 | Vinyl chloride resin composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH08295773A true JPH08295773A (en) | 1996-11-12 |
Family
ID=14362704
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10377095A Pending JPH08295773A (en) | 1995-04-27 | 1995-04-27 | Vinyl chloride resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH08295773A (en) |
-
1995
- 1995-04-27 JP JP10377095A patent/JPH08295773A/en active Pending
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