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JPH0448819B2 - - Google Patents
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JPH0448819B2 - - Google Patents

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Publication number
JPH0448819B2
JPH0448819B2 JP58005719A JP571983A JPH0448819B2 JP H0448819 B2 JPH0448819 B2 JP H0448819B2 JP 58005719 A JP58005719 A JP 58005719A JP 571983 A JP571983 A JP 571983A JP H0448819 B2 JPH0448819 B2 JP H0448819B2
Authority
JP
Japan
Prior art keywords
vinyl chloride
parts
weight
chloride resin
plasticizer
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.)
Expired - Lifetime
Application number
JP58005719A
Other languages
Japanese (ja)
Other versions
JPS59129245A (en
Inventor
Toshiaki Kobayashi
Hiroyuki Matsushima
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.)
Zeon Corp
Original Assignee
Nippon Zeon 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 Nippon Zeon Co Ltd filed Critical Nippon Zeon Co Ltd
Priority to JP571983A priority Critical patent/JPS59129245A/en
Publication of JPS59129245A publication Critical patent/JPS59129245A/en
Publication of JPH0448819B2 publication Critical patent/JPH0448819B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、高滑性軟質塩化ビニル樹脂組成物に
関し、更に詳しくは塩化ビニル樹脂、ポリオレフ
イン系樹脂、塩素化ポリエチレンおよび可塑剤と
からなる塩化ビニル樹脂組成物に関するものであ
る。 一般に塩化ビニル樹脂に可塑剤他を配合してな
る軟質塩化ビニル樹脂組成物は、柔軟でゴム様弾
性を有し、すぐれた成形性を持つとともに安価な
こともあり、広範囲な用途に使用されている。そ
の用途の一つである自動車窓ガラスのウエザース
トリツプ部材は、窓枠部に取付けて、窓ガラス面
と接触せしめ、室内へ風雨が侵入するのを防ぐ目
的を持つ部品であり、密着性を要求されることか
ら、軟質塩化ビニル樹脂又はゴムの押出成形物が
使用されている。一方、このウエザーストリツプ
部材は密着性と同時に、窓ガラスの開閉が容易に
行なえるよう、ガラスとの接触部は摩擦抵抗が出
来るだけ小さいことも要求される。しかし、従来
の軟質塩化ビニル樹脂組成物あるいはゴムでは摩
擦抵抗が大きく、そのままでは使用できない。従
つて、製造工程が増え、コストアツプになるにも
かかわらず、ガラス面との接触部分に植毛あるい
は摩擦抵抗の低い塗料の塗布という手法が現在使
われている。そのため軟質塩化ビニル樹脂組成物
自体で摩擦抵抗のきわめて低い材料が開発される
ことが強く望まれている。 本発明者は、この問題について種々検討を重ね
た結果、塩化ビニル樹脂にポリオレフイン系樹
脂、特定の塩素化ポリエチレンおよび可塑剤を添
加することにより、摩擦抵抗のきわめて低い組成
物が得られることを見出し、本発明を完成するに
至つた。 すなわち本発明は、塩化ビニル樹脂100重量部
に対し、ポリオレフイン系樹脂10〜300重量部、
結晶化度5%以上、塩素化度10〜50%の塩素化ポ
リエチレン0.1〜5重量部および可塑剤を配合し
てなり、かつJIS硬度(JISK−6301A型)が50〜
95であることを特徴とする高滑性軟質塩化ビニル
樹脂組成物である。 本発明において用いられる塩化ビニル樹脂と
は、塩化ビニルの単独重合物の他、塩化ビニルと
エチレン、酢酸ビニル、塩化ビニリデン、ビニル
エーテル類等とを共重合させた塩化ビニルを主体
とした共重合物或いは塩化ビニル−エチレン−酢
酸ビニル等のグラフト共重合物の単独あるいは二
種以上の混合物のことである。 また、ポリオレフイン系樹脂とは、低密度ポリ
エチレン、高密度ポリエチレン、ポリプロビレ
ン、エチレン−プロピレンコポリマー、ポリブテ
ン、ポリイソブチレン、ポリ4−メチルペンテン
−1等のポリオレフイン樹脂単独及び二種以上の
混合物のことである。ポリオレフイン系樹脂の添
加量が塩化ビニル樹脂100重量部に対し、10重量
部未満では十分な摩擦抵抗の低下を期待出来ず、
300重量部を越えると硬度が上り過ぎて可塑剤だ
けで低下させることが難かしく、又、折曲げ白化
現象も十分抑制できない。 本発明における塩素化ポリエチレンとは、結晶
化度5%以上で、塩素化度10〜50%のものをい
う。結晶化度5%未満のもの、および塩素化度1
%未満又は50%を越えるものではいずれも折曲げ
白化現象を十分抑制できない。又、塩化ビニル樹
脂100重量部に対し、塩素化ポリエチレンの添加
量が0.1重量部未満では十分に折曲げ白化現象を
抑制できず、5重量部を越えると、摩擦抵抗の低
下をむしろ抑制する方向となり好ましくない。 本発明における可塑剤とは、塩化ビニル樹脂の
軟質用途に一般に使われる可塑剤のことであつ
て、ジオクチルフタレート、ジイソデシルフタレ
ート、ジブチルフタレート、ジヘプチルフタレー
ト等のフタル酸エステル、ジオクチルアジペー
ト、ジオクチルセバケート等の直鎖二塩基酸エス
テル、トリメリツト酸エステル、ポリエステル系
高分子可塑剤、エポキシ化大豆油、エポキシ化ア
マニ油等のエポキシ系可塑剤、トリフエニルフオ
スフアイト等のリン酸エステル系可塑剤等の単独
又は二種以上を混合したものが使用される。可塑
剤の添加によりJIS硬度(JISK−6301A型)を50
〜95としたのは50未満では軟らかすぎて実用的で
なく、かつ、十分な摩擦抵抗の低下を得られない
こと、又硬度95を越えると硬すぎて、軟質用とし
て使用できないためである。 なお、本発明の組成物にオルガノポリシロキサ
ンを塩化ビニル樹脂100重量部当たり0.1〜10重量
部の範囲で含有せしめると摩擦抵抗がさらに低下
するので好ましい。オルガノポリシロキサンの例
としては、ジメチルポリシロキサン、メチルフエ
ニルポリシロキサン、メチルハイドロジエンポリ
シロキサン等、及び下記に示す各種変性ポリシロ
キサン(w、x、y、zは整数)等の単独又は二
種以上を混合したものが使用される。 本発明の組成物は、既述した成分の他に安定
剤、充填剤、酸化防止剤、紫外線吸収剤、滑剤、
加工助剤、顔料、難燃剤等を必要に応じ含有する
ことが出来る。 本発明の高滑性軟塩化ビニル組成物は、押出成
形、射出成形、カレンダー成形、中空成形等、通
常の方法により成形することができる。 なお、従来軟質塩化ビニル樹脂にポリオレフイ
ン系樹脂を添加することは知られているが(特開
昭48−5842)、この組成物では引裂強度が低下し、
しかも折曲げ白化現象が起ることを避けられな
い。また、塩化ビニル樹脂、ポリオレフイン樹脂
混合物に塩素化ポリエチレン、無機充填剤を添加
する樹脂組成物も公知(特開昭51−12855)であ
るが、この方法は、組成物の均一相溶性及び脆性
防止のために塩素化ポリエチレンを塩化ビニル樹
脂100重量部当たり約5.5重量部以上添加すること
を必須要件としている。それに対して本発明にお
いては、可塑剤及び特定の塩素化ポリエチレンを
用いるので、塩素化ポリエチレンの使用量は0.1
〜5重量部という少量で均一に相溶した組成物を
得ることができるばかりでなく、この範囲より多
量用いた場合には高滑性の成形品を与えることが
できないのである。さらに、前記公知の方法は摩
擦抵抗の低下を意図するものではない。 以下、本発明を実施例により、さらに詳しく説
明する。なお、実施例で示す部数は特にことわら
ない限り、重量部である。 実施例 1 第1表に示す樹脂、可塑剤及び添加剤の表示部
数を配合し、155℃の熱ロールにて5分間混練し、
シート状に取り出した後、表面粗さが中心線平均
粗さ(Ra)(JISB−0601)で2.3μmのツヤ消し面
を有するプレス板にて160℃、5分間加熱プレス
し、厚さ2mm、直径60mmの円板を打ち抜き、試験
片を作成し、下記方法により試験した。結果を第
1表に示す。 静摩擦係数は、平滑なガラス面にツヤ消し面を
ガラス面に接する様に置き、重量が100gとなる
様荷重を乗せ、ガラス面を徐々に傾けていき、試
験片の動き出した角度より求めた。 折曲げ白化性は、試験片を180度曲げた時、屈
曲面に白化が生じるか否かを目視、判定した。 硬度は、JISK−6301A型にて測定した。
The present invention relates to a highly slippery soft vinyl chloride resin composition, and more particularly to a vinyl chloride resin composition comprising a vinyl chloride resin, a polyolefin resin, a chlorinated polyethylene, and a plasticizer. In general, soft vinyl chloride resin compositions made by blending vinyl chloride resin with plasticizers and other ingredients are flexible, have rubber-like elasticity, have excellent moldability, and are inexpensive, so they are used in a wide range of applications. There is. Weather strips for automobile window glass, one of its uses, are parts that are attached to the window frame and come into contact with the window glass surface to prevent wind and rain from entering the room. Therefore, extrusion molded products of soft vinyl chloride resin or rubber are used. On the other hand, this weather strip member is required not only to have good adhesion but also to have as little frictional resistance as possible at the contact portion with the glass so that the window glass can be opened and closed easily. However, conventional soft vinyl chloride resin compositions or rubbers have high frictional resistance and cannot be used as they are. Therefore, methods such as flocking or applying a paint with low frictional resistance to the contact area with the glass surface are currently used, although this increases the number of manufacturing steps and costs. Therefore, it is strongly desired that a soft vinyl chloride resin composition itself with extremely low frictional resistance be developed. As a result of various studies regarding this problem, the present inventor discovered that a composition with extremely low frictional resistance can be obtained by adding a polyolefin resin, a specific chlorinated polyethylene, and a plasticizer to a vinyl chloride resin. , we have completed the present invention. That is, the present invention uses 10 to 300 parts by weight of polyolefin resin to 100 parts by weight of vinyl chloride resin,
Contains 0.1 to 5 parts by weight of chlorinated polyethylene with a crystallinity of 5% or more and a chlorination degree of 10 to 50% and a plasticizer, and has a JIS hardness (JISK-6301A type) of 50 to 50.
95. This is a highly slippery flexible vinyl chloride resin composition characterized by having a polyvinyl chloride resin composition of 95%. The vinyl chloride resin used in the present invention is not only a vinyl chloride homopolymer, but also a vinyl chloride-based copolymer obtained by copolymerizing vinyl chloride with ethylene, vinyl acetate, vinylidene chloride, vinyl ethers, etc. It refers to a graft copolymer such as vinyl chloride-ethylene-vinyl acetate or a mixture of two or more thereof. Furthermore, polyolefin resin refers to polyolefin resins such as low-density polyethylene, high-density polyethylene, polypropylene, ethylene-propylene copolymer, polybutene, polyisobutylene, poly-4-methylpentene-1, etc., and a mixture of two or more thereof. . If the amount of polyolefin resin added is less than 10 parts by weight per 100 parts by weight of vinyl chloride resin, a sufficient reduction in frictional resistance cannot be expected.
If the amount exceeds 300 parts by weight, the hardness increases so much that it is difficult to reduce it with a plasticizer alone, and the phenomenon of whitening upon bending cannot be sufficiently suppressed. The chlorinated polyethylene in the present invention has a crystallinity of 5% or more and a chlorination degree of 10 to 50%. Crystallinity less than 5% and chlorination degree 1
If it is less than 50% or more than 50%, the whitening phenomenon cannot be sufficiently suppressed. Furthermore, if the amount of chlorinated polyethylene added to 100 parts by weight of vinyl chloride resin is less than 0.1 part by weight, it will not be possible to sufficiently suppress the bending whitening phenomenon, and if it exceeds 5 parts by weight, the reduction in frictional resistance will be suppressed. This is undesirable. The plasticizer in the present invention refers to a plasticizer that is generally used for soft vinyl chloride resins, and includes phthalic acid esters such as dioctyl phthalate, diisodecyl phthalate, dibutyl phthalate, and diheptyl phthalate, dioctyl adipate, and dioctyl sebacate. linear dibasic acid esters such as trimellitic acid esters, polyester polymer plasticizers, epoxy plasticizers such as epoxidized soybean oil and epoxidized linseed oil, phosphate ester plasticizers such as triphenyl phosphorite, etc. They may be used alone or in combination of two or more. JIS hardness (JISK-6301A type) is 50 by adding plasticizer.
The reason why the hardness is set at ~95 is that if it is less than 50, it is too soft to be practical and the frictional resistance cannot be reduced sufficiently, and if the hardness exceeds 95, it is too hard and cannot be used as a soft material. It is preferred that the composition of the present invention contain organopolysiloxane in an amount of 0.1 to 10 parts by weight per 100 parts by weight of vinyl chloride resin, since this further reduces the frictional resistance. Examples of organopolysiloxanes include dimethylpolysiloxane, methylphenylpolysiloxane, methylhydrodienepolysiloxane, etc., and various modified polysiloxanes shown below (w, x, y, z are integers), etc. alone or in combination. A mixture of the above is used. In addition to the above-mentioned components, the composition of the present invention also includes stabilizers, fillers, antioxidants, ultraviolet absorbers, lubricants,
Processing aids, pigments, flame retardants, etc. can be contained as necessary. The highly slippery soft vinyl chloride composition of the present invention can be molded by conventional methods such as extrusion molding, injection molding, calendar molding, and blow molding. Although it has been known to add polyolefin resin to soft vinyl chloride resin (Japanese Patent Application Laid-Open No. 1986-5842), this composition has a lower tear strength and
Moreover, the phenomenon of whitening due to bending cannot be avoided. In addition, a resin composition in which chlorinated polyethylene and an inorganic filler are added to a mixture of vinyl chloride resin and polyolefin resin is also known (Japanese Patent Application Laid-Open No. 12855/1985), but this method can achieve uniform compatibility and prevent brittleness of the composition. Therefore, it is an essential requirement that chlorinated polyethylene be added in an amount of about 5.5 parts by weight or more per 100 parts by weight of vinyl chloride resin. In contrast, in the present invention, a plasticizer and a specific chlorinated polyethylene are used, so the amount of chlorinated polyethylene used is 0.1
Not only can a homogeneously compatible composition be obtained with a small amount of ~5 parts by weight, but a molded article with high lubricity cannot be obtained when a larger amount is used than this range. Furthermore, the known method is not intended to reduce frictional resistance. Hereinafter, the present invention will be explained in more detail with reference to Examples. Note that the numbers shown in the examples are parts by weight unless otherwise specified. Example 1 The indicated parts of the resin, plasticizer and additives shown in Table 1 were blended and kneaded for 5 minutes with a hot roll at 155°C.
After taking out the sheet, it was hot pressed at 160℃ for 5 minutes on a press plate with a matte surface with a center line average roughness (Ra) (JISB-0601) of 2.3 μm, and the sheet was heated to a thickness of 2 mm. A disk with a diameter of 60 mm was punched out to prepare a test piece, and the test piece was tested according to the following method. The results are shown in Table 1. The coefficient of static friction was determined by placing the matte surface on a smooth glass surface so that it was in contact with the glass surface, placing a load such that the weight was 100 g, gradually tilting the glass surface, and determining the angle at which the test piece began to move. The bending whitening property was determined by visually observing whether or not whitening occurred on the bent surface when the test piece was bent 180 degrees. Hardness was measured using JISK-6301A model.

【表】【table】

【表】 *1 ○は白化なし、×は白化あり
実施例 2 ポリジメチルシロキサン添加系の実施例を第2
表に示す。樹脂、可塑剤及び添加剤を表示部数配
合し、以下、実施例1と同様の方法にて試験片を
作成し、測定も同様に行なつた。結果を第2表に
示す。
[Table] *1 ○ means no whitening, × means whitening Example 2 Example of polydimethylsiloxane addition system
Shown in the table. A resin, a plasticizer, and an additive were mixed in the indicated amounts, and a test piece was prepared in the same manner as in Example 1, and measurements were performed in the same manner. The results are shown in Table 2.

【表】【table】

【表】 *1 第1表と同じ
[Table] *1 Same as Table 1

Claims (1)

【特許請求の範囲】 1 塩化ビニル樹脂100重量部に対し、ポリオレ
フイン系樹脂10〜300重量部、結晶化度5%以上、
塩素化度10〜50%の塩素化ポリエチレン0.1〜5
重量部および可塑剤を配合してなり、かつJIS硬
度(JISK−6301A型)が50〜95であることを特
徴とするウエザーストリツプ部材用高滑性軟質塩
化ビニル樹脂組成物。 2 塩化ビニル樹脂100重量部に対し、ポリオレ
フイン系樹脂10〜300重量部、結晶化度5%以上、
塩素化度10〜50%の塩素化ポリエチレン0.1〜5
重量部、オルガノポリシロキサン0.1〜10重量部
および可塑剤を配合してなり、かつJIS硬度
(JISK−6301A型)が50〜95であることを特徴と
するウエザーストリツプ部材用高滑性軟質塩化ビ
ニル樹脂組成物。
[Scope of Claims] 1. 10 to 300 parts by weight of polyolefin resin based on 100 parts by weight of vinyl chloride resin, crystallinity of 5% or more,
Chlorinated polyethylene with degree of chlorination 10-50% 0.1-5
1. A highly slippery soft vinyl chloride resin composition for a weather strip member, characterized in that it contains parts by weight and a plasticizer, and has a JIS hardness (JISK-6301A type) of 50 to 95. 2. For 100 parts by weight of vinyl chloride resin, 10 to 300 parts by weight of polyolefin resin, crystallinity of 5% or more,
Chlorinated polyethylene with degree of chlorination 10-50% 0.1-5
A highly lubricating soft material for weather strip members, which contains 0.1 to 10 parts by weight of organopolysiloxane and a plasticizer, and has a JIS hardness (JISK-6301A type) of 50 to 95. Vinyl chloride resin composition.
JP571983A 1983-01-17 1983-01-17 Highly slippery soft vinyl chloride resin composition Granted JPS59129245A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP571983A JPS59129245A (en) 1983-01-17 1983-01-17 Highly slippery soft vinyl chloride resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP571983A JPS59129245A (en) 1983-01-17 1983-01-17 Highly slippery soft vinyl chloride resin composition

Publications (2)

Publication Number Publication Date
JPS59129245A JPS59129245A (en) 1984-07-25
JPH0448819B2 true JPH0448819B2 (en) 1992-08-07

Family

ID=11618923

Family Applications (1)

Application Number Title Priority Date Filing Date
JP571983A Granted JPS59129245A (en) 1983-01-17 1983-01-17 Highly slippery soft vinyl chloride resin composition

Country Status (1)

Country Link
JP (1) JPS59129245A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103740001A (en) * 2013-12-26 2014-04-23 吴江市东泰电力特种开关有限公司 PVC (polyvinyl chloride) wear-resistant switch

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4500469B2 (en) * 2001-07-23 2010-07-14 中部電力株式会社 COMPOSITE RESIN COMPOSITION, PROCESS FOR PRODUCING THE SAME, AND MOLDED ARTICLE THEREOF

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5112855A (en) * 1974-04-17 1976-01-31 Sumitomo Bakelite Co JUSHI SEIBUTSU
JPS5765742A (en) * 1980-10-08 1982-04-21 Mitsubishi Petrochem Co Ltd Conductive resin composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103740001A (en) * 2013-12-26 2014-04-23 吴江市东泰电力特种开关有限公司 PVC (polyvinyl chloride) wear-resistant switch

Also Published As

Publication number Publication date
JPS59129245A (en) 1984-07-25

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