JPH05148396A - Vinyl chloride resin composition for integral molding of glass with vinyl chloride resin, and integrally molded glass-vinyl chloride resin article - Google Patents

Vinyl chloride resin composition for integral molding of glass with vinyl chloride resin, and integrally molded glass-vinyl chloride resin article

Info

Publication number
JPH05148396A
JPH05148396A JP3316387A JP31638791A JPH05148396A JP H05148396 A JPH05148396 A JP H05148396A JP 3316387 A JP3316387 A JP 3316387A JP 31638791 A JP31638791 A JP 31638791A JP H05148396 A JPH05148396 A JP H05148396A
Authority
JP
Japan
Prior art keywords
vinyl chloride
chloride resin
glass
weight
resin 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
Application number
JP3316387A
Other languages
Japanese (ja)
Inventor
Shigeru Tanaka
茂 田中
Wataru Aono
渉 青野
Hiroshi Kakei
博志 加計
Hironobu Nakamura
裕信 中村
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.)
Sekisui Chemical Co Ltd
Original Assignee
Sekisui Chemical 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 Sekisui Chemical Co Ltd filed Critical Sekisui Chemical Co Ltd
Priority to JP3316387A priority Critical patent/JPH05148396A/en
Publication of JPH05148396A publication Critical patent/JPH05148396A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Injection Moulding Of Plastics Or The Like (AREA)

Abstract

PURPOSE:To prepare the subject compsn. which is excellent in flowability during injection molding and gives a molded article having a nontacky surface and a high surface hardness by compounding a vinyl chloride resin with a plasticizer and a specific hydrogenated terpene resin. CONSTITUTION:100 pts.wt. vinyl chloride resin is compounded with 20-150 pts.wt. plasticizer and 1-10 pts.wt. hydrogenated terpene resin of the formula having a number-average mol.wt. of 400-1,000 to give the objective compsn., which is excellent in flowability during injection molding and gives a molded article having a nontacky surface and a high surface hardness. Replacing the terpene resin in the above compsn. with 1-20 pts.wt. glass balloons having a mean diameter of 50-200mum or with 5-40 pts.wt. ethylene-vinyl acetate copolymer having a vinyl acetate content of 50-80wt.% and a melt flow rate (JIS 6730) of 40-250g/10 min gives a compsn. having properties equivalent to those of the above compsn.

Description

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

【0001】[0001]

【産業上の利用分野】本発明は車両、建築物等に用いら
れるガラス・塩化ビニル系樹脂一体成形用塩化ビニル系
樹脂組成物及びそれを用いたガラス・塩化ビニル系樹脂
一体成形体に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a vinyl chloride resin composition for glass / vinyl chloride resin integral molding used in vehicles, buildings and the like, and a glass / vinyl chloride resin integral molding using the same.

【0002】[0002]

【従来の技術】一般に、自動車用のリアウインド、クォ
ーターウインド等の窓材に使用される枠材(以下モール
という)としては、ゴム、塩化ビニル樹脂等が用いられ
ている。
2. Description of the Related Art Generally, rubber, vinyl chloride resin or the like is used as a frame material (hereinafter referred to as a molding) used for window materials such as rear windows and quarter windows for automobiles.

【0003】従来、これら窓材は、ガラスをシール材を
介して車体の枠体にはめ込んだ後、モールを取り付ける
方式によって、車体に装着されていたが、この方式は手
作業が主体の上、工程数も多いため経済的ではなかっ
た。
Conventionally, these window members have been mounted on the vehicle body by a method in which a glass is fitted into a frame body of a vehicle body through a sealing material and then a molding is attached thereto. It was not economical due to the large number of processes.

【0004】上記問題を解決するために、種々の方法が
提案されており、例えば、特開昭62−68992号公
報、特開平2−60722号公報等には、ガラス・塩化
ビニル樹脂一体成形方式(以下、モジュ−ルウインド方
式という)、即ち、ガラスを射出成形機の金型内にセッ
トし、ガラス周縁部に塩化ビニル樹脂からなる枠材を一
体に成形し、得られた窓材を車体に装着する方法が提案
されている。
In order to solve the above problems, various methods have been proposed. For example, in JP-A-62-68992 and JP-A-2-60722, a glass / vinyl chloride resin integral molding method is proposed. (Hereinafter, referred to as a module window method), that is, glass is set in a mold of an injection molding machine, a frame material made of vinyl chloride resin is integrally molded on the peripheral edge of the glass, and the obtained window material is used as a vehicle body. A method of mounting is proposed.

【0005】上記モジュールウインド方式に用いられる
塩化ビニル樹脂としては、塩化ビニル単独重合体に可塑
剤を添加した組成物が使用されている。しかしながら、
この組成物は、射出成形時の流動性が悪いため、ガラス
周縁部を塩化ビニル樹脂の射出成形体で完全に覆うには
射出圧、型締圧等を高くする必要があり、その結果、ガ
ラスが強い圧力で締め付けられ、ガラスが破損し易いと
いう欠点があった。
As the vinyl chloride resin used in the above module window system, a composition obtained by adding a plasticizer to a vinyl chloride homopolymer is used. However,
Since this composition has poor fluidity during injection molding, it is necessary to increase injection pressure, mold clamping pressure, etc. in order to completely cover the glass peripheral edge with an injection molded product of vinyl chloride resin. However, there was a drawback that the glass was apt to be damaged due to being tightened with a strong pressure.

【0006】一方、射出成形時の塩化ビニル樹脂の流動
性を向上させる方法としては、塩化ビニル樹脂の重合度
を下げることが試みられているが、低重合度の塩化ビニ
ル樹脂を用いると流動性は向上するものの、可塑剤の保
持性能が低下するため、得られた射出成形体内部から可
塑剤がブリードアウトし、その結果、射出成形体の機械
的物性が低下したり、射出成形体表面がタック性を帯び
るという欠点があった。
On the other hand, as a method for improving the fluidity of the vinyl chloride resin at the time of injection molding, it has been attempted to lower the polymerization degree of the vinyl chloride resin. However, the plasticizer bleeding out from the inside of the obtained injection-molded product results in a decrease in the mechanical properties of the injection-molded product or the surface of the injection-molded product is deteriorated. It had the drawback of being tacky.

【0007】[0007]

【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、射出成形時の流動性に優れ
たガラス・塩化ビニル系樹脂一体成形用塩化ビニル系樹
脂組成物及び機械的物性に優れ、かつ表面にタック性の
ないガラス・塩化ビニル系樹脂一体成形体を提供するこ
とを目的とする。
SUMMARY OF THE INVENTION The present invention has been made in view of the above-mentioned drawbacks, and is a vinyl chloride resin composition and a machine for glass / vinyl chloride resin integral molding excellent in fluidity during injection molding. It is an object of the present invention to provide a glass / vinyl chloride resin integrated molding having excellent physical properties and having no tackiness on the surface.

【0008】[0008]

【課題を解決するための手段】発明1の塩化ビニル系樹
脂組成物は、塩化ビニル系樹脂100重量部と、可塑剤
20〜150重量部と、次式(1)で表される数平均分
子量が400〜1000の水素化テルペン樹脂1〜10
重量部からなることを特徴としている。
The vinyl chloride resin composition of Invention 1 comprises 100 parts by weight of a vinyl chloride resin, 20 to 150 parts by weight of a plasticizer, and a number average molecular weight represented by the following formula (1). Of 400-1000 hydrogenated terpene resin 1-10
It is characterized by being composed of parts by weight.

【0009】[0009]

【化2】 [Chemical 2]

【0010】発明2の塩化ビニル系樹脂組成物は、塩化
ビニル系樹脂100重量部と、可塑剤20〜150重量
部と、平均粒径が50〜200μmのガラス中空球1〜
20重量部からなることを特徴としている。
The vinyl chloride resin composition of Invention 2 comprises 100 parts by weight of a vinyl chloride resin, 20 to 150 parts by weight of a plasticizer, and glass hollow spheres 1 to 50 having an average particle diameter of 50 to 200 μm.
It is characterized by comprising 20 parts by weight.

【0011】また、発明3の塩化ビニル系樹脂組成物
は、塩化ビニル系樹脂100重量部と、可塑剤20〜1
50重量部と、酢酸ビニル含有量が50〜80重量%で
あってメルトフローレート(JIS K6730)が4
0〜250(gr/10分)であるエチレン−酢酸ビニ
ル共重合体5〜40重量部からなることを特徴としてい
る。
The vinyl chloride resin composition of the third aspect of the present invention comprises 100 parts by weight of a vinyl chloride resin and 20 to 1 of a plasticizer.
50 parts by weight and a vinyl acetate content of 50 to 80% by weight and a melt flow rate (JIS K6730) of 4
It is characterized by comprising 5 to 40 parts by weight of an ethylene-vinyl acetate copolymer having a content of 0 to 250 (gr / 10 minutes).

【0012】そして、発明4のガラス・塩化ビニル系樹
脂一体成形体は、射出成形によって上記の塩化ビニル系
樹脂組成物がガラスの周縁部に一体的に形成されている
ものであることを特徴としている。
The glass / vinyl chloride resin integrally molded article of the invention 4 is characterized in that the above vinyl chloride resin composition is integrally formed on the peripheral portion of the glass by injection molding. There is.

【0013】本発明で用いられる塩化ビニル系樹脂とし
ては、塩化ビニルの単独重合体の他に、射出成形時の塩
化ビニル系樹脂組成物の流動性、最終的に得られる成形
体の機械的物性等が低下しない範囲内で、塩化ビニル
と、塩化ビニルと共重合可能な重合性単量体との共重合
体、または、塩化ビニルと共重合可能な重合性樹脂に塩
化ビニルをグラフトさせたグラフト共重合体等があげら
れる。なお、共重合体中の上記重合性単量体あるいは重
合性樹脂で形成される構成単位の含有量は、40重量%
を超えないことが好ましい。
The vinyl chloride resin used in the present invention includes, in addition to vinyl chloride homopolymer, the fluidity of the vinyl chloride resin composition at the time of injection molding and the mechanical properties of the finally obtained molded product. Etc. within the range that does not decrease, a copolymer of vinyl chloride and a polymerizable monomer copolymerizable with vinyl chloride, or a grafted vinyl chloride grafted onto a polymerizable resin copolymerizable with vinyl chloride. Examples thereof include copolymers. The content of the structural unit formed of the above polymerizable monomer or polymerizable resin in the copolymer is 40% by weight.
It is preferable not to exceed.

【0014】上記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るものでなく、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、ブチルビニルエーテル、セチルビニルエーテ
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、フェニルメタクリレ
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、塩化ビニリデン、フッ
化ビニル等のハロゲン化ビニル類、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
イミド類などがあげられる。これらは、単独で使用され
てもよいし、2種以上併用されてもよい。
The polymerizable monomer is not particularly limited as long as it has a reactive double bond, and examples thereof include α-olefins such as ethylene, propylene and butylene, vinyl acetate and propionic acid. Vinyl esters such as vinyl, vinyl ethers such as butyl vinyl ether and cetyl vinyl ether, acrylic acid esters such as methyl acrylate and ethyl acrylate, methacrylic acid esters such as methyl methacrylate, ethyl methacrylate and phenyl methacrylate, styrene, α-methylstyrene And the like, vinylidene chloride, vinyl halides such as vinyl fluoride, and N-substituted maleimides such as N-phenylmaleimide and N-cyclohexylmaleimide. These may be used alone or in combination of two or more.

【0015】また、上記重合性樹脂としては、特に限定
されるものではなく、例えば、エチレン−酢酸ビニル共
重合体、エチレン−酢酸ビニル−一酸化炭素共重合体、
エチレン−エチルアクリレート共重合体、エチレン−エ
チルアクリレート−一酸化炭素共重合体、エチレン−メ
チルメタクリレート共重合体、エチレン−プロピレン共
重合体、アクリルニトリル−ブタジエン共重合体、ポリ
ウレタン樹脂、塩素化ポリエチレン樹脂、塩素化ポリプ
ロピレン樹脂などがあげられる。これらは、単独で使用
されてもよいし、2種以上併用されてもよい。
The above-mentioned polymerizable resin is not particularly limited, and examples thereof include ethylene-vinyl acetate copolymer, ethylene-vinyl acetate-carbon monoxide copolymer,
Ethylene-ethyl acrylate copolymer, ethylene-ethyl acrylate-carbon monoxide copolymer, ethylene-methyl methacrylate copolymer, ethylene-propylene copolymer, acrylonitrile-butadiene copolymer, polyurethane resin, chlorinated polyethylene resin , Chlorinated polypropylene resin and the like. These may be used alone or in combination of two or more.

【0016】この塩化ビニル系樹脂の平均重合度は、小
さくなると最終的に得られる成形体の機械的物性が低下
するとともに、可塑剤の保持力が低下して成形体表面が
タック性を有し、大きくなると射出成形時の塩化ビニル
系樹脂組成物の流動性が低下するので、400〜150
0が好ましい。
If the average degree of polymerization of this vinyl chloride resin becomes small, the mechanical properties of the molded product finally obtained will deteriorate, and the holding power of the plasticizer will also decrease and the surface of the molded product will have tackiness. If it becomes large, the fluidity of the vinyl chloride resin composition at the time of injection molding decreases, so 400 to 150
0 is preferred.

【0017】そして、塩化ビニル系樹脂の製造方法は任
意の方法が採用されてよく、例えば、ラジカル重合開始
剤を用いて塩化ビニルの重合で通常行われている公知の
懸濁重合法、乳化重合法、溶液重合法、塊状重合法等が
あげられる。懸濁重合法は、得られる重合体に不純物が
含まれ難く、また製造コストが比較的安価なことから好
適に採用される。
Any method may be adopted as the method for producing the vinyl chloride resin, for example, a well-known suspension polymerization method or emulsion weight method which is usually used in the polymerization of vinyl chloride using a radical polymerization initiator. Examples include a legal method, a solution polymerization method, and a bulk polymerization method. The suspension polymerization method is preferably used because impurities are unlikely to be contained in the obtained polymer and the production cost is relatively low.

【0018】本発明で用いられる可塑剤としては、上記
の塩化ビニル系樹脂と相溶性のあるものであれば特に限
定されるものではなく、例えば、フタル酸ジエチル、フ
タル酸ジ−n−オクチル、フタル酸ジイソデシル等のフ
タル酸系、アジピン酸ジブチル、アジピン酸ジ−n−ヘ
キシル等のアジピン酸系、リン酸トリブチル、リン酸ト
リ−2−エチルヘキシル等のリン酸系、トリメリット酸
トリブチル、トリメリット酸トリ−2−エチルヘキシル
等のトリメリット酸系、塩素化パラフィン系、ポリエス
テル系等があげられるが、特に、揮発性が少なく、耐フ
ォギング性に優れたフタル酸ジイソデシル(以下、DI
DPという)及びトリメリット酸トリ−2−エチルヘキ
シル(以下、TOTMという)が好適に用いられる。こ
れらは、単独で使用されてもよいし、2種以上併用され
てもよい。
The plasticizer used in the present invention is not particularly limited as long as it is compatible with the vinyl chloride resin, and examples thereof include diethyl phthalate and di-n-octyl phthalate. Phthalates such as diisodecyl phthalate, dibutyl adipate, adipic acid such as di-n-hexyl adipate, tributyl phosphate, phosphates such as tri-2-ethylhexyl phosphate, tributyl trimellitate, trimellitate Examples include trimellitic acid-based acid such as tri-2-ethylhexyl acid, chlorinated paraffin-based, polyester-based, etc., but especially diisodecyl phthalate (hereinafter, referred to as DI with low volatility and excellent fogging resistance).
DP) and tri-2-ethylhexyl trimellitate (hereinafter referred to as TOTM) are preferably used. These may be used alone or in combination of two or more.

【0019】このような可塑剤の添加量は、少なくなる
と射出成形時の流動性が低下し、多くなると最終的に得
られる成形体表面にタック性が現れるので、上記塩化ビ
ニル系樹脂100重量部に対して20〜150重量部で
ある。
When the amount of such a plasticizer added is small, the fluidity at the time of injection molding decreases, and when it is large, tackiness appears on the surface of the finally obtained molded product, so 100 parts by weight of the above vinyl chloride resin is used. 20 to 150 parts by weight.

【0020】本発明1において用いられる上式(1)で
表されるテルペン樹脂は、数平均分子量が400〜10
00のものとされるのは、その数平均分子量が400未
満であると、その水素化テルペン樹脂は非常に脆くな
り、これを添加した塩化ビニル系樹脂組成物による成形
体はその機械強度が低下し、逆に1000を超える水素
化テルペン樹脂の粘度が高くなり、そのためこれを添加
した塩化ビニル系樹脂組成物は、熱溶融時の流動性が悪
く成形性が低下するからである。なお、この数平均分子
量はGPC法による測定値からの算出値を意味する。
The terpene resin represented by the above formula (1) used in the present invention 1 has a number average molecular weight of 400 to 10
When the number average molecular weight is less than 400, the hydrogenated terpene resin becomes extremely brittle, and the molded product made of the vinyl chloride resin composition to which it is added has a lower mechanical strength. On the contrary, the viscosity of the hydrogenated terpene resin of more than 1000 becomes high, so that the vinyl chloride resin composition to which the hydrogenated terpene resin is added has poor fluidity at the time of heat melting and deteriorates moldability. In addition, this number average molecular weight means the calculated value from the measured value by the GPC method.

【0021】この水素化テルペン樹脂は、単独で使用さ
れる他、2種類以上併用することも可能であり、その添
加量は、上記のとおり、塩化ビニル系樹脂100重量部
に対して1〜10重量部とされるのは、1重量部未満で
あると射出成形時の塩化ビニル系樹脂組成物の流動性が
十分でなく、10重量部を超えると得られる成形体の機
械的物性が低下するからである。
This hydrogenated terpene resin can be used alone or in combination of two or more kinds, and the addition amount thereof is 1 to 10 with respect to 100 parts by weight of vinyl chloride resin as described above. When the amount is less than 1 part by weight, the fluidity of the vinyl chloride resin composition at the time of injection molding is insufficient, and when it exceeds 10 parts by weight, the mechanical properties of the obtained molded article deteriorate. Because.

【0022】本発明2において用いられるガラス中空球
の組成は特に限定されるものでなく、主成分であるSi
2 の他、Al2 3 、B2 3 、Fe2 3 、Na2
O、K2 O、MgO、CaO、TiO2 、BaO、Mn
O等が任意の割合で含有していてもよい。また、その表
面にコーティング処理やカップリング処理を施すことに
より、塩化ビニル系樹脂との相溶性や粘着性を向上させ
てもよい。
The composition of the glass hollow spheres used in the present invention 2 is not particularly limited, and Si as the main component is used.
In addition to O 2 , Al 2 O 3 , B 2 O 3 , Fe 2 O 3 , Na 2
O, K 2 O, MgO, CaO, TiO 2 , BaO, Mn
O and the like may be contained in an arbitrary ratio. In addition, compatibility or adhesion with the vinyl chloride resin may be improved by subjecting the surface to a coating treatment or a coupling treatment.

【0023】このガラス中空球の平均粒径は、50〜2
00μmのものとされるのは、平均粒径が50μm未満
であったり、逆に200μmを超えると、そのような粒
径のガラス中空球を添加した塩化ビニル系樹脂組成物の
熱溶融時の流動性は改良されないからである。
The average particle diameter of the glass hollow spheres is 50 to 2
If the average particle size is less than 50 μm, or if it exceeds 200 μm, the flow of the vinyl chloride resin composition containing glass hollow spheres having such a particle size at the time of heat melting is defined as 00 μm. This is because the sex is not improved.

【0024】このガラス中空球は、単独で使用されても
よいし、2種以上併用することも可能であり、その添加
量は、上記のとおり、塩化ビニル系樹脂100重量部に
対し1〜20重量部とされるのは、1重量部未満である
と射出成形時の流動性が低下し、20重量部を超えると
最終的に得られる成形体の機械的物性が低下するととも
に、射出成形時の流動性も低下するからである。
The glass hollow spheres may be used alone or in combination of two or more, and the addition amount thereof is 1 to 20 per 100 parts by weight of the vinyl chloride resin as described above. When the amount is less than 1 part by weight, the fluidity at the time of injection molding is reduced, and when it exceeds 20 parts by weight, the mechanical properties of the finally obtained molded article are deteriorated and at the time of injection molding. This is because the liquidity of is also reduced.

【0025】発明3において用いられるエチレン−酢酸
ビニル共重合体は、上記のとおり、酢酸ビニル含有量が
50〜80重量%とされるのは、50重量%未満である
と塩化ビニル系樹脂との相溶性が低下するとともに機械
的物性が低下し、80重量%を超えると塩化ビニル系樹
脂との相溶性は向上するが流動性が低下するとともに得
られる成形体の柔軟性や耐候性が低下するからであり、
より好ましくは55〜70重量%である。また、そのメ
ルトフローレートが上記のとおり40〜250(gr/
10分)とされるのは、40(gr/10分)未満であ
ると塩化ビニル系樹脂組成物の流動性が向上せず、25
0(gr/10分)を超えると得られる成形体の機械的
物性が低下するからであり、より好ましくは100〜1
50(gr/10分)である。なお、このメルトフロー
レートの値は、JISK6730による測定値である。
As described above, the ethylene-vinyl acetate copolymer used in the invention 3 has a vinyl acetate content of 50 to 80% by weight when it is less than 50% by weight with a vinyl chloride resin. When the compatibility is lowered, the mechanical properties are lowered, and when it exceeds 80% by weight, the compatibility with the vinyl chloride resin is improved but the fluidity is lowered and the flexibility and weather resistance of the obtained molded article are lowered. From
It is more preferably 55 to 70% by weight. In addition, the melt flow rate is 40 to 250 (gr /
If it is less than 40 (gr / 10 minutes), the fluidity of the vinyl chloride-based resin composition is not improved, and it is 25 minutes.
This is because if it exceeds 0 (gr / 10 minutes), the mechanical properties of the obtained molded article deteriorate, and more preferably 100 to 1
It is 50 (gr / 10 minutes). The value of the melt flow rate is a value measured by JISK6730.

【0026】このエチレン−酢酸ビニル共重合体は、単
独で使用されてもよいし、2種以上併用することも可能
であり、その添加量は、上記のとおり、塩化ビニル系樹
脂100重量部に対し5〜40重量部とされるのは、少
なくなると射出成形時の流動性が低下し、多くなると得
られる成形体の機械的物性、耐候性、柔軟性が低下する
からであり、より好ましくは10〜20重量部である。
This ethylene-vinyl acetate copolymer may be used alone or in combination of two or more kinds, and the addition amount thereof is 100 parts by weight of vinyl chloride resin as described above. The amount of 5 to 40 parts by weight, on the other hand, is because when the amount is reduced, the fluidity during injection molding is lowered, and when the amount is increased, the mechanical properties, weather resistance and flexibility of the obtained molded article are reduced, and more preferably. 10 to 20 parts by weight.

【0027】本発明1〜3の塩化ビニル系樹脂組成物に
は、必要に応じて、ブチル錫マレ−ト、オクチル錫マレ
−ト等の錫系安定剤、ステアリン酸カルシウム、ステア
リン酸バリウム、ステアリン酸亜鉛等の有機金属塩系安
定剤、金属石ケン系安定剤、エポキシ化大豆油、エポキ
シ化アマニ油等の有機エポキシ化合物系安定剤等の熱安
定剤、ポリエチレンワックス、パラフィンワックス等の
脂肪族炭化水素系滑剤、ステアリルアルコール等の高級
脂肪族アルコール系滑剤、ステアリン酸、ヒドロキシス
テアリン酸等の高級脂肪酸系滑剤、脂肪酸アマイド系滑
剤、脂肪酸エステル系滑剤等の滑剤、ベンゾフェノン系
紫外線吸収剤、ベンゾトリアゾール系紫外線吸収剤等の
紫外線吸収剤、アクリル系加工助剤、ハロゲン系難燃
剤、リン系難燃剤等の難燃剤、炭酸カルシウム、クレ
ー、マイカ等の充填剤、酸化チタン、カーボンブラック
等の顔料等が添加されてもよい。
In the vinyl chloride resin compositions of the present inventions 1 to 3, if necessary, tin stabilizers such as butyltin maleate and octyltin maleate, calcium stearate, barium stearate, stearic acid. Organic metal salt stabilizers such as zinc, metal soap stabilizers, heat stabilizers such as organic epoxy compound stabilizers such as epoxidized soybean oil and epoxidized linseed oil, and aliphatic carbonization such as polyethylene wax and paraffin wax. Hydrogen lubricant, higher aliphatic alcohol lubricant such as stearyl alcohol, higher fatty acid lubricant such as stearic acid and hydroxystearic acid, fatty acid amide lubricant, lubricant such as fatty acid ester lubricant, benzophenone ultraviolet absorber, benzotriazole lubricant UV absorbers such as UV absorbers, acrylic processing aids, halogen flame retardants, phosphorus flame retardants, etc. Flame retardants, calcium carbonate, clay, filler such as mica, titanium oxide, pigments such as carbon black may be added.

【0028】ガラス・塩化ビニル系樹脂一体成形体の製
造方法は任意の方法が採用されてよいが、射出成形によ
り成形されるのが好ましい。本発明4のガラス・塩化ビ
ニル系樹脂一体成形体は、本発明1〜3の塩化ビニル系
樹脂組成物が射出成形され、ガラスの周縁部に一体的に
形成されたものである。
Although any method may be adopted as the method for producing the glass / vinyl chloride resin integrally-molded article, it is preferably injection-molded. The glass / vinyl chloride resin integrated molding of the present invention 4 is formed by injection molding the vinyl chloride resin composition of the present inventions 1 to 3 and integrally formed on the peripheral portion of the glass.

【0029】上記ガラスとしては、特に限定されるもの
ではなく、例えば、自動車用強化ガラス、自動車用合わ
せガラス等の加工ガラス、建築用未加工ガラスなどがあ
げられる。これらのガラスは、金型内に設置され、その
周縁部に上記塩化ビニル系樹脂組成物が射出成形され一
体化されるが、ガラスと塩化ビニル系樹脂組成物との接
着性をより向上させるために、ガラス周縁部の塩化ビニ
ル系樹脂組成物と接触するガラス表面に、エポキシ系樹
脂接着剤、フェノ−ル変性エポキシ系樹脂接着剤、ポリ
アミド系樹脂接着剤等の公知のガラス・塩化ビニル系樹
脂組成物接着用接着剤の層を予め設けた後、塩化ビニル
系樹脂組成物を射出成形してもよい。
The above-mentioned glass is not particularly limited, and examples thereof include tempered glass for automobiles, processed glass such as laminated glass for automobiles, and unprocessed glass for construction. These glasses are placed in a mold, and the vinyl chloride resin composition is injection-molded and integrated into the periphery of the glass to improve the adhesion between the glass and the vinyl chloride resin composition. On the glass surface in contact with the vinyl chloride resin composition on the periphery of the glass, a known glass / vinyl chloride resin such as an epoxy resin adhesive, a phenol-modified epoxy resin adhesive, a polyamide resin adhesive, etc. A vinyl chloride resin composition may be injection-molded after a layer of an adhesive for adhering the composition is provided in advance.

【0030】上記射出成形の方式としては、上記塩化ビ
ニル系樹脂組成物を加熱分解させることなく射出成形で
きるものであれば特に限定されるものではなく、例え
ば、プランジャ方式、プランジャ・プリプラ方式、スク
リュ・プリプラ方式、スクリュ・イン・ライン方式等が
あげられ、プランジャ方式が好適に用いられる。
The injection molding method is not particularly limited as long as it can be injection molded without thermally decomposing the vinyl chloride resin composition, and examples thereof include a plunger method, a plunger / preparer method, and a screw. -A pre-plasticizer method, a screw-in-line method, etc. are mentioned, and a plunger method is preferably used.

【0031】上記プランジャ方式の射出成形は、加熱し
たシリンダ中で上記塩化ビニル系樹脂組成物を加熱流動
化し、これを押出ラムにより金型中にプランジャで押し
込む成形法である。
The plunger type injection molding is a molding method in which the vinyl chloride resin composition is heated and fluidized in a heated cylinder, and the composition is pushed into the mold by an extrusion ram with a plunger.

【0032】上記プランジャ方式の射出成形において
は、射出成形機のシリンダ内の圧力は100〜300Kg
/cm2 とするのが好ましく、また射出成形機シリンダ内
の塩化ビニル系樹脂組成物は、160〜200℃で溶融
状態とされ、これを金型のキャビティ内に充填するのが
好ましい。
In the above-mentioned plunger type injection molding, the pressure in the cylinder of the injection molding machine is 100 to 300 kg.
/ Cm 2 is preferable, and it is preferable that the vinyl chloride resin composition in the cylinder of the injection molding machine is in a molten state at 160 to 200 ° C., and this is filled in the cavity of the mold.

【0033】以下、図面を参照し、塩化ビニル系樹脂組
成物を射出成形してガラス周縁部に一体的に成形体を形
成する工程を説明する。図1は本発明4のガラス・塩化
ビニル系樹脂一体成形体を射出成形して製造する工程を
例示する模式断面図である。
The process of injection molding a vinyl chloride resin composition to integrally form a molded body on the peripheral portion of the glass will be described below with reference to the drawings. FIG. 1 is a schematic cross-sectional view illustrating a process of producing a glass / vinyl chloride resin integrated molding of the present invention 4 by injection molding.

【0034】図1において、3は上型31と下型32か
らなる金型であり、金型3には溶融状態の塩化ビニル系
樹脂組成物21を注入する樹脂注入口34と金型冷却用
冷却水パイプ33が設置されている。35は上型31と
下型32により形成されたキャビティであり、ガラス1
を挟持する中央空隙部37と溶融状態の塩化ビニル系樹
脂組成物21を充填するための周縁空隙部36とから形
成されている。
In FIG. 1, reference numeral 3 denotes a mold composed of an upper mold 31 and a lower mold 32. The mold 3 has a resin injection port 34 for injecting the molten vinyl chloride resin composition 21 and a mold cooling die. A cooling water pipe 33 is installed. Reference numeral 35 denotes a cavity formed by the upper mold 31 and the lower mold 32.
And a peripheral cavity portion 36 for filling the molten vinyl chloride resin composition 21.

【0035】以下、製造方法を説明する。まず、図1
(イ)に示すように、ガラス1を中央空隙部37に配置
し、金型を閉じる。次に図1(ロ)に示すように、金型
3を型締めした後に周縁空隙部36に溶融状態の塩化ビ
ニル系樹脂組成物21を樹脂注入口34より注入してキ
ャビティ35内に溶融状態の塩化ビニル系樹脂組成物2
1を充填し、冷却水パイプ33に冷却水を流して金型3
を冷却すると、図1(ハ)に示すように、周縁空隙部3
6に注入された溶融状態の塩化ビニル系樹脂組成物21
が冷却固化され、塩化ビニル系樹脂成形体2がガラス1
の周縁部に一体的に形成される。次いで、図1(ニ)に
示すように、金型3を開いて取り出すと、ガラス1と塩
化ビニル系樹脂成形体2が一体的に射出成形されたガラ
ス・塩化ビニル系樹脂一体成形体Aが得られる。
The manufacturing method will be described below. First, Fig. 1
As shown in (a), the glass 1 is placed in the central cavity 37 and the mold is closed. Next, as shown in FIG. 1B, after the mold 3 is clamped, the molten vinyl chloride resin composition 21 is injected into the peripheral cavity 36 through the resin injection port 34 and the molten state is formed in the cavity 35. Vinyl chloride resin composition 2
1 and then the cooling water is flowed through the cooling water pipe 33 to mold 3
When cooled, as shown in FIG.
Molten vinyl chloride resin composition 21 injected into No. 6
Is cooled and solidified, and the vinyl chloride resin molded body 2 becomes the glass 1
Is integrally formed on the peripheral portion of the. Next, as shown in FIG. 1D, when the mold 3 is opened and taken out, a glass / vinyl chloride resin integrated molding A in which the glass 1 and the vinyl chloride resin molding 2 are integrally injection-molded is obtained. can get.

【0036】[0036]

【実施例】以下、本発明の実施例を説明する。なお、
「部」とあるのは「重量部」を意味する。また、結果に
示した塩化ビニル系樹脂組成物およびガラス・塩化ビニ
ル系樹脂一体成形体に関する各物性の測定方法は次の通
りである。 1.塩化ビニル系樹脂組成物に関する物性 (1)流動性 得られた塩化ビニル系樹脂組成物をペレット化し、高化
式フローテスタ(島津製作所社製、型式;CFT−50
0)に供給して、170℃、100kgf/cm2 荷重の条件
下で1φ×10mmのノズルを使用して測定した。 (2)引張強度 得られた塩化ビニル系樹脂組成物を160℃の8インチ
ロールに供給し、組成物がロールに巻きついた後、3分
間溶融混練し、ロールシートを得た。得られたロールシ
ートを、170℃で3分間予熱した後、50Kg/cm2で4
分加圧し、その後冷却プレスして厚さ2mmの塩化ビニル
系樹脂板を得た。得られた樹脂板を用いJIS K67
45に準拠して測定した。 (3)タック性 引張強度の測定に使用したのと同じ塩化ビニル系樹脂板
を70℃、95%RHの雰囲気下に1週間放置した後、
その表面の状態を22℃、65%RHの雰囲気下で官能
検査して下記の判定基準によりタック性を評価した。
EXAMPLES Examples of the present invention will be described below. In addition,
"Parts" means "parts by weight". The methods for measuring the physical properties of the vinyl chloride-based resin composition and the glass / vinyl chloride-based resin integrated molding shown in the results are as follows. 1. Physical Properties of Vinyl Chloride Resin Composition (1) Fluidity The obtained vinyl chloride resin composition is pelletized, and a Koka type flow tester (manufactured by Shimadzu Corporation, model: CFT-50) is used.
No. 1) and was measured at 170 ° C. under a load of 100 kgf / cm 2 using a 1φ × 10 mm nozzle. (2) Tensile Strength The obtained vinyl chloride resin composition was supplied to an 8-inch roll at 160 ° C., the composition was wrapped around the roll, and melt-kneaded for 3 minutes to obtain a roll sheet. The obtained roll sheet is preheated at 170 ° C. for 3 minutes and then at 4 kg at 50 kg / cm 2 .
After pressurizing for a minute and then cooling and pressing, a vinyl chloride resin plate having a thickness of 2 mm was obtained. JIS K67 using the obtained resin plate
It measured based on 45. (3) Tackiness After leaving the same vinyl chloride resin plate used for the measurement of tensile strength for 1 week in an atmosphere of 70 ° C. and 95% RH,
The surface state was subjected to a sensory test in an atmosphere of 22 ° C. and 65% RH, and tackiness was evaluated according to the following criteria.

【0037】:タック性なし ×:試料表面がベタついた状態であり、タック性有り (4)ショア硬度 引張強度の測定に使用したのと同じ塩化ビニル系樹脂板
を用いて、その表面の硬度をショア硬度計(上島製作所
製、型式;HD−103N)により測定した。 (5)エチレン−酢酸ビニル共重合体のメルトフローレ
ート エチレン−酢酸ビニル共重合体の粉末について、JIS
K6730に従って試験温度190℃、試験荷重2.
16kgf(21.18N)の条件下で10分間にノズ
ルを流れるエチレン−酢酸ビニルの量(cc)を測定し
た。 2.ガラス・塩化ビニル系樹脂一体成形体に関する物性 (1)耐ショートショット性 得られたガラス・塩化ビニル系樹脂一体成形体を目視観
察して、下記の判定基準により耐ショートショット性を
評価した。
: No tackiness x: The surface of the sample is solid and has tackiness. (4) Shore hardness Using the same vinyl chloride resin plate as used for the measurement of tensile strength, the hardness of the surface Was measured by a Shore hardness meter (Kamishima Seisakusho, model: HD-103N). (5) Melt Flow Rate of Ethylene-Vinyl Acetate Copolymer For powders of ethylene-vinyl acetate copolymer, JIS
Test temperature 190 ° C. according to K6730, test load 2.
The amount (cc) of ethylene-vinyl acetate flowing through the nozzle was measured for 10 minutes under the condition of 16 kgf (21.18 N). 2. Physical Properties of Glass / Vinyl Chloride Resin Integrated Molding (1) Short Shot Resistance The obtained glass / vinyl chloride resin integrated molding was visually observed to evaluate the short shot resistance according to the following criteria.

【0038】○:ガラス周縁部の塩化ビニル系樹脂組成
物の成形体が欠落のない状態で存在する。 ×:ガラス周縁部の塩化ビニル系樹脂組成物の成形体が
一部欠落してショートショット状態で存在する (2)タック性 得られたガラス・塩化ビニル系樹脂一体成形体を70
℃、95%RHの雰囲気下に1週間放置した後、塩化ビ
ニル系樹脂組成物の成形体表面の状態を22℃、65%
RHの雰囲気下で官能検査して下記の判定基準によりタ
ック性を評価した。
◯: A molded product of the vinyl chloride resin composition at the peripheral portion of the glass exists in a state where there is no omission. X: A part of the molded product of the vinyl chloride resin composition at the peripheral portion of the glass is missing and exists in a short shot state. (2) Tackiness The obtained molded product of glass and vinyl chloride resin is 70
After leaving for 1 week in an atmosphere of 95 ° C. and 95% RH, the surface state of the molded product of the vinyl chloride resin composition is kept at 22 ° C. and 65%.
A sensory test was conducted in an atmosphere of RH, and tackiness was evaluated according to the following criteria.

【0039】○:タック性なし ×:試料表面がベタついた状態であり、タック性有り実施例1〜6、比較例1〜5 表1に示した所定量の塩化ビニル樹脂、可塑剤、水素化
テルペン樹脂(ヤロハラケミカル社製、クリアロンP1
05;GPC法による数平均分子量630又はクリアロ
ンP125;GPC法による数平均分子量700)と、
バリウム−亜鉛系液状安定剤(旭電化社製、商品名;A
C−190)1.5部、バリウム−亜鉛系粉末状安定剤
(旭電化社製、商品名;AP−550)0.5部及び有
機エポキシ化合物系安定剤(旭電化社製、商品名;O−
130P)3.0部をスーパーミキサー(川田製作所社
製、型式;SMG−100)に供給し、100℃まで昇
温しながら20分間攪拌した後、内容物をクーリングミ
キサー(川田製作所社製、型式;CO−100)に移
し、15分間攪拌し、30℃以下まで冷却してコンパウ
ンドを得た。
◯: No tackiness ×: The surface of the sample is solid and tacky. Examples 1 to 6 and Comparative Examples 1 to 5 Predetermined amounts of vinyl chloride resin, plasticizer, and hydrogen shown in Table 1. Terpene resin (Yarohara Chemical Co., Clearon P1
05; number average molecular weight 630 by GPC method or Clearon P125; number average molecular weight 700 by GPC method),
Barium-zinc liquid stabilizer (Asahi Denka Co., Ltd., trade name; A
C-190) 1.5 parts, barium-zinc powder stabilizer (Asahi Denka Co., Ltd., trade name; AP-550) 0.5 parts and organic epoxy compound stabilizer (Asahi Denka Co., Ltd. trade name; O-
130P) 3.0 parts was supplied to a super mixer (manufactured by Kawada Seisakusho, model; SMG-100) and stirred for 20 minutes while heating to 100 ° C., and then the contents were cooled by a mixer (manufactured by Kawada Seisakusho, model). CO-100), stirred for 15 minutes and cooled to 30 ° C or lower to obtain a compound.

【0040】得られたコンパウンドを金型温度およびバ
レル先端温度が155℃に設定された押出機(長田製作
所社製、型式;SLM−50)に供給し、溶融混練して
押出物を得た。
The obtained compound was supplied to an extruder (manufactured by Nagata Seisakusho, model: SLM-50) in which the mold temperature and the barrel tip temperature were set to 155 ° C., and melt-kneaded to obtain an extrudate.

【0041】得られた押出物を冷却した後、コールドカ
ットペレタイザー(ユニオン・プラスチック社製、型
式;UC−152)に供給し、カッティングしてペレッ
ト状の塩化ビニル系樹脂組成物を得た。
After cooling the obtained extrudate, it was supplied to a cold cut pelletizer (manufactured by Union Plastics, model: UC-152) and cut to obtain a pelletized vinyl chloride resin composition.

【0042】得られた塩化ビニル系樹脂組成物を用い
て、前記測定法に基づき、塩化ビニル系樹脂組成物に関
する各物性を測定した。結果を表1に示した。次いで、
射出成形機(東芝機械社製、型式;IS−350E)に
設置された金型内に、周縁部にエポキシ系樹脂接着剤
(セメダイン社製、商品名;セメダイン1500)層を
幅1cm、厚さ25μmに形成したガラス(300×30
0×3mmの大きさの強化ガラス)を配置し型締した後、
上記ペレット状の塩化ビニル系樹脂組成物を上記射出成
形機に供給し、上記塩化ビニル系樹脂組成物を190℃
に加温して溶融し、樹脂注入口よりシリンダー内圧力1
70Kg/cm2 で注入して上記溶融状態の塩化ビニル系樹
脂組成物をキャビティ内に充填した。
Using the obtained vinyl chloride resin composition, various physical properties of the vinyl chloride resin composition were measured based on the above-mentioned measuring methods. The results are shown in Table 1. Then
An epoxy resin adhesive (made by Cemedine, trade name; Cemedine 1500) layer at the peripheral portion is 1 cm wide and thick in a mold installed in an injection molding machine (Toshiba Machinery, model; IS-350E). Glass formed to 25 μm (300 × 30
After arranging 0 x 3 mm size tempered glass) and clamping,
The pelletized vinyl chloride resin composition is supplied to the injection molding machine, and the vinyl chloride resin composition is heated to 190 ° C.
It is heated to melt and melted, and the pressure in the cylinder from the resin injection port is 1
It was injected at 70 kg / cm 2 to fill the cavity with the molten vinyl chloride resin composition.

【0043】次に、金型冷却用の冷却水パイプに冷却水
を流して金型を冷却し、キャビティ内の溶融塩化ビニル
系樹脂組成物を冷却固化させた後、型を開いて取り出
し、ガラス・塩化ビニル系樹脂一体成形体を得た。
Next, cooling water is flowed through a cooling water pipe for cooling the mold to cool the mold, and the molten vinyl chloride resin composition in the cavity is cooled and solidified.・ A vinyl chloride resin integrated molding was obtained.

【0044】得られたガラス・塩化ビニル系樹脂一体成
形体を用いて、前記測定法に基づき、ガラス・塩化ビニ
ル系樹脂一体成形体に関する各物性を測定した。結果を
表1に示した。
Using the obtained glass / vinyl chloride resin integrally molded body, various physical properties of the glass / vinyl chloride resin integrally molded body were measured based on the above-mentioned measuring methods. The results are shown in Table 1.

【0045】[0045]

【表1】 [Table 1]

【0046】実施例7〜12、比較例6〜9 表2に示すとおり、水素化テルペン樹脂の代わりにガラ
ス中空球を使用した他は上記実施例と同様にして、塩化
ビニル系樹脂組成物及びガラス・塩化ビニル系樹脂一体
成形体を得、各物性を測定した。結果を表2に示した。
Examples 7 to 12 and Comparative Examples 6 to 9 As shown in Table 2, a vinyl chloride resin composition and a vinyl chloride resin composition were prepared in the same manner as in the above Examples except that glass hollow spheres were used instead of the hydrogenated terpene resin. A glass / vinyl chloride resin integrated molding was obtained, and its physical properties were measured. The results are shown in Table 2.

【0047】[0047]

【表2】 [Table 2]

【0048】実施例13〜18、比較例10〜12 表3に示すとおり、水素化テルペン樹脂の代わりにエチ
レン−酢酸ビニル共重合体を使用した他は実施例1と同
様にして、塩化ビニル系樹脂組成物及びガラス・塩化ビ
ニル系樹脂一体成形体を得、各物性を測定した。結果を
表3に示した。
Examples 13 to 18 and Comparative Examples 10 to 12 As shown in Table 3 , the procedure of Example 1 was repeated except that an ethylene-vinyl acetate copolymer was used in place of the hydrogenated terpene resin, and a vinyl chloride resin was used. A resin composition and a glass / vinyl chloride resin integrally molded body were obtained, and each physical property was measured. The results are shown in Table 3.

【0049】[0049]

【表3】 [Table 3]

【0050】[0050]

【発明の効果】本発明の塩化ビニル系樹脂組成物の構成
は前記した通りであり、本発明1に記載の塩化ビニル系
樹脂組成物は、塩化ビニル系樹脂に、可塑剤と特定の水
素化テルペン樹脂とが特定量配合されているから、射出
成形時の流動性に優れ、かつ上記塩化ビニル系樹脂組成
物を用いて作製した成形体表面はタック性がなく、表面
硬度が優れている。
The constitution of the vinyl chloride resin composition of the present invention is as described above, and the vinyl chloride resin composition of the present invention 1 comprises a vinyl chloride resin, a plasticizer and a specific hydrogenation. Since the terpene resin is blended in a specific amount, it has excellent fluidity at the time of injection molding, and the surface of the molded article produced using the above vinyl chloride resin composition has no tackiness and excellent surface hardness.

【0051】本発明2に記載の塩化ビニル系樹脂組成物
は、塩化ビニル系樹脂に、可塑剤と特定粒径のガラス中
空球とが特定量配合されているから、射出成形時の流動
性に優れ、かつ上記塩化ビニル系樹脂組成物を用いて作
製した成形体表面はタック性がなく、表面硬度が優れて
いる。
Since the vinyl chloride resin composition according to the second aspect of the present invention contains a vinyl chloride resin and a plasticizer and glass hollow spheres having a specific particle size in a specific amount, it has a fluidity during injection molding. In addition, the surface of the molded article produced using the above vinyl chloride resin composition is not tacky and has excellent surface hardness.

【0052】本発明3に記載の塩化ビニル系樹脂組成物
は、塩化ビニル系樹脂に、可塑剤と特定のエチレン−酢
酸ビニル共重合体とが特定量配合されているから、射出
成形時の流動性に優れ、かつ上記塩化ビニル系樹脂組成
物を用いて作製した成形体表面はタック性がなく、表面
硬度が優れている。
The vinyl chloride resin composition according to the third aspect of the present invention contains a vinyl chloride resin containing a plasticizer and a specific ethylene-vinyl acetate copolymer in a specific amount. The surface of the molded article produced by using the above vinyl chloride-based resin composition has no tackiness and excellent surface hardness.

【0053】本発明4のガラス・塩化ビニル系樹脂一体
成形体は、本発明1〜3の塩化ビニル系樹脂組成物がガ
ラスの周縁部に射出成形されたものであるから、射出成
形時に塩化ビニル系樹脂組成物が優れた流動性を示し、
射出圧、型締圧等を上げなくてもガラス周縁部に塩化ビ
ニル系樹脂組成物が完全に回り込み、ショートショット
状態とならず、ガラス周縁部の塩化ビニル系樹脂組成物
の成形体が欠落していないガラス・塩化ビニル系樹脂一
体成形体を得ることができ、得られたガラス・塩化ビニ
ル系樹脂一体成形体の塩化ビニル系樹脂成形体表面はタ
ック性を示さない。
Since the glass / vinyl chloride resin integrated molding of the present invention 4 is obtained by injection-molding the vinyl chloride resin composition of the present inventions 1 to 3 on the peripheral portion of the glass, the vinyl chloride resin molding at the time of injection molding is carried out. The resin composition shows excellent fluidity,
Even if the injection pressure, mold clamping pressure, etc. are not increased, the vinyl chloride resin composition completely wraps around the glass peripheral edge, the short shot state does not occur, and the molded product of the vinyl chloride resin composition around the glass peripheral edge is missing. It is possible to obtain a glass / vinyl chloride resin integrated molded body which is not formed, and the surface of the obtained glass / vinyl chloride resin integrated molded body does not exhibit tackiness.

【図面の簡単な説明】[Brief description of drawings]

【図1】図1(イ)、(ロ)、(ハ)および(ニ)は請
求項2のガラス・塩化ビニル系樹脂一体成形体を射出成
形して製造する工程を例示する模式断面図である。
1 (a), (b), (c), and (d) are schematic cross-sectional views illustrating a process of injection molding the glass / vinyl chloride resin integrated molding of claim 2. is there.

【符号の説明】[Explanation of symbols]

A ガラス・塩化ビニル系樹脂一体成形体 1 ガラス 2 塩化ビニル系樹脂成形体 3 金型 A glass / vinyl chloride resin molded body 1 glass 2 vinyl chloride resin molded body 3 mold

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 B29K 27:06 105:20 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area B29K 27:06 105: 20

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 塩化ビニル系樹脂100重量部と、可塑
剤20〜150重量部と、次式(1)で表される数平均
分子量が400〜1000の水素化テルペン樹脂1〜1
0重量部からなることを特徴とするガラス・塩化ビニル
系樹脂一体成形用塩化ビニル系樹脂組成物。 【化1】
1. 100 parts by weight of a vinyl chloride resin, 20 to 150 parts by weight of a plasticizer, and hydrogenated terpene resins 1-1 having a number average molecular weight of 400 to 1000 represented by the following formula (1).
A vinyl chloride resin composition for glass / vinyl chloride resin integral molding, which comprises 0 part by weight. [Chemical 1]
【請求項2】 塩化ビニル系樹脂100重量部と、可塑
剤20〜150重量部と、平均粒径が50〜200μm
のガラス中空球1〜20重量部からなることを特徴とす
るガラス・塩化ビニル系樹脂一体成形用塩化ビニル系樹
脂組成物。
2. A vinyl chloride resin of 100 parts by weight, a plasticizer of 20 to 150 parts by weight, and an average particle size of 50 to 200 μm.
1. A vinyl chloride resin composition for glass / vinyl chloride resin integral molding, comprising 1 to 20 parts by weight of the glass hollow sphere.
【請求項3】 塩化ビニル系樹脂100重量部と、可塑
剤20〜150重量部と、酢酸ビニル含有量が50〜8
0重量%であってメルトフローレート(JIS673
0)が40〜250(gr/10分)であるエチレン−
酢酸ビニル共重合体5〜40重量部からなることを特徴
とするガラス・塩化ビニル系樹脂一体成形用塩化ビニル
系樹脂組成物。
3. 100 parts by weight of a vinyl chloride resin, 20 to 150 parts by weight of a plasticizer, and a vinyl acetate content of 50 to 8
It is 0% by weight and has a melt flow rate (JIS673
0) is 40-250 (gr / 10 min) ethylene-
A vinyl chloride resin composition for glass / vinyl chloride resin integrated molding, which comprises 5 to 40 parts by weight of a vinyl acetate copolymer.
【請求項4】 請求項1、請求項2又は請求項3に記載
の塩化ビニル系樹脂組成物が射出成形され、ガラスの周
縁部に一体的に形成されていることを特徴とするガラス
・塩化ビニル系樹脂一体成形体。
4. A glass / chlorine characterized in that the vinyl chloride resin composition according to claim 1, 2 or 3 is formed by injection molding and is integrally formed on the peripheral portion of the glass. Vinyl resin integrated molding.
JP3316387A 1991-11-29 1991-11-29 Vinyl chloride resin composition for integral molding of glass with vinyl chloride resin, and integrally molded glass-vinyl chloride resin article Pending JPH05148396A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3316387A JPH05148396A (en) 1991-11-29 1991-11-29 Vinyl chloride resin composition for integral molding of glass with vinyl chloride resin, and integrally molded glass-vinyl chloride resin article

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3316387A JPH05148396A (en) 1991-11-29 1991-11-29 Vinyl chloride resin composition for integral molding of glass with vinyl chloride resin, and integrally molded glass-vinyl chloride resin article

Publications (1)

Publication Number Publication Date
JPH05148396A true JPH05148396A (en) 1993-06-15

Family

ID=18076520

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3316387A Pending JPH05148396A (en) 1991-11-29 1991-11-29 Vinyl chloride resin composition for integral molding of glass with vinyl chloride resin, and integrally molded glass-vinyl chloride resin article

Country Status (1)

Country Link
JP (1) JPH05148396A (en)

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