JPH0798879B2 - Polypropylene resin composition - Google Patents
Polypropylene resin compositionInfo
- Publication number
- JPH0798879B2 JPH0798879B2 JP61250644A JP25064486A JPH0798879B2 JP H0798879 B2 JPH0798879 B2 JP H0798879B2 JP 61250644 A JP61250644 A JP 61250644A JP 25064486 A JP25064486 A JP 25064486A JP H0798879 B2 JPH0798879 B2 JP H0798879B2
- Authority
- JP
- Japan
- Prior art keywords
- resin composition
- polypropylene
- polypropylene resin
- weight
- present
- 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
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- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は物性の良好なポリプロピレン樹脂組成物に関す
る。詳しくは、特定の化合物を含むポリプロピレン樹脂
組成物に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a polypropylene resin composition having good physical properties. Specifically, it relates to a polypropylene resin composition containing a specific compound.
ポリプロピレンは比較的耐熱性、剛性に優れた安価な樹
脂であるが、比較的結晶化度が小さい為通常の方法で成
型したのでは、成型物の剛性が樹脂本体のものに比較し
て不良であるという問題があった。これに対しては、種
々の核剤を添加する方法が知られており、中でも特定の
高分子化合物を添加する方法(例えば、特開昭60−1397
31号公報)は添加物が成型物表面に浮きだすといった問
題もなく、しかも比較的少量の添加で効果的であるなど
優れた方法である。Polypropylene is an inexpensive resin that has relatively high heat resistance and rigidity, but since it has a relatively low degree of crystallinity, it can be molded with a normal method and the rigidity of the molded product is poorer than that of the resin body. There was a problem. On the other hand, a method of adding various nucleating agents is known, and among them, a method of adding a specific polymer compound (for example, JP-A-60-1397).
No. 31) is an excellent method in which there is no problem that the additive floats on the surface of the molded product, and the addition of a relatively small amount is effective.
高分子化合物を添加する方法は優れているのであるが、
開示された高分子化合物はその合成方法が難しく、入手
し難たいという問題があるために他の有用な化合物の開
発が望まれている。Although the method of adding a polymer compound is excellent,
The disclosed polymer compounds are difficult to synthesize and difficult to obtain. Therefore, development of other useful compounds is desired.
本発明者らは、ポリプロピレンの結晶化度を向上させる
新たな化合物について鋭意探索し、特定の化合物がその
目的に適うものであることを見出し、本発明を完成し
た。The present inventors have intensively searched for a new compound that improves the crystallinity of polypropylene, found that a specific compound is suitable for the purpose, and completed the present invention.
即ち、本発明は主鎖が珪素であり、しかも珪素1原子当
たり1個以上の炭化水素残基を有する有機ポリシランを
含有することを特徴とするポリプロピレン樹脂組成物で
ある。That is, the present invention is a polypropylene resin composition characterized in that the main chain is silicon and contains an organic polysilane having one or more hydrocarbon residues per silicon atom.
本発明において、ポリプロピレンとしては結晶性のポリ
プロピレンであるかぎりプロピレンの単独重合体のみな
らずエチレン、ブテン−1、ヘキセン−1等の他のオレ
フィンとのランダム、或いは、ブロック共重合体であっ
てもよく、公知のチーグラー・ナッタ触媒を用いプロピ
レンを重合することで製造でき、また市場で広く入手す
ることもできる。In the present invention, the polypropylene is not only a homopolymer of propylene as long as it is a crystalline polypropylene, but also a random copolymer with other olefins such as ethylene, butene-1, and hexene-1, or a block copolymer. Often, it can be produced by polymerizing propylene using a known Ziegler-Natta catalyst, and is also widely available on the market.
本発明において、有機ポリシランとしては、主鎖が珪素
であり、しかも珪素1原子当たり1個以上の炭化水素残
基を有するものである。例えば、ジハロゲン化シランを
ナトリウム等で脱塩素重縮合することで製造することが
できる(例えば、R.C.West,Comprehensive Organic Che
mstry,Vol.2,Chapter 9.4,P365〜387(1982),edited b
y G.Willkinson et al.,Pergamon Press,New York)。
具体的には、ポリフェニルメチルシラン、ポリフェネチ
ルメチルシラン、ポリプロピルメチルシラン、ポリブチ
ルメチルシラン、ポリヘキシルメチルシラン、ポリドデ
シルメチルシラン、ポリシクロヘキシルメチルシラン、
ポリジヘキシルシラン、ポリジブチルシラン、ポリジペ
チルシラン等が例示される。In the present invention, the organic polysilane has a main chain of silicon and has one or more hydrocarbon residues per silicon atom. For example, it can be produced by dechlorination polycondensation of a dihalogenated silane with sodium or the like (for example, RCWest, Comprehensive Organic Che
mstry, Vol.2, Chapter 9.4, P365 ~ 387 (1982), edited b
y G. Willkinson et al., Pergamon Press, New York).
Specifically, polyphenylmethylsilane, polyphenethylmethylsilane, polypropylmethylsilane, polybutylmethylsilane, polyhexylmethylsilane, polydodecylmethylsilane, polycyclohexylmethylsilane,
Examples thereof include polydihexylsilane, polydibutylsilane, and polydipetylsilane.
本発明において上記ポリプロピレンとポリシランの混合
方法については特に制限はなく、単に両者を混合溶融す
る方法、或いはポリシランを含む触媒を用いてポリプロ
ピレンを重合しポリシランを分散せしめる方法などが挙
げられる。ここで、ポリシランのポリプロピレンに対す
る割合としては0.00001〜10重量%好しくは0.0001〜1
重量%である。0.00001重量%未満では添加の効果が殆
どなく、また、10重量%を越して添加しても格別その効
果は増大しない。In the present invention, the method of mixing the polypropylene and the polysilane is not particularly limited, and examples thereof include a method of simply mixing and melting the two and a method of polymerizing polypropylene using a catalyst containing polysilane to disperse polysilane. Here, the ratio of polysilane to polypropylene is 0.00001 to 10% by weight, preferably 0.0001 to 1
% By weight. If it is less than 0.00001% by weight, there is almost no effect of addition, and if it is added in excess of 10% by weight, the effect is not particularly increased.
以下、実施例をあげ本発明を更に説明する。 Hereinafter, the present invention will be further described with reference to examples.
実施例1 3のオートクーブにn−ヘプタン1、丸紅ソルベー
社製三塩化チタン触媒(TGY−24)300mgおよびジエチル
アルミニウムクロライド1mlを入れ、プロピレンガスを
挿入して5kg/cm2とし、水素0.4Nlを加えたのち加熱して
内温を70℃とた。プロピレンを挿入ながら圧力を5kg/cm
2として3時間重合した。メタノールで触媒を失活し、
水洗して触媒残分を除去し、濾過乾燥してパウダーを得
た。得られたパウダーは850gであり、極限粘度は1.78
(135℃テトラリン溶液で測定)、沸騰n−ヘプタン抽
出残率は98.2%(熊川式抽出器を用いて6時間抽出)で
あった。Example 1 Autoclave of Example 3 was charged with n-heptane 1, 300 mg of titanium trichloride catalyst (TGY-24) manufactured by Marubeni Solvay Co., Ltd. and 1 ml of diethylaluminum chloride, propylene gas was introduced to make 5 kg / cm 2, and 0.4 Nl of hydrogen was added. After the addition, heating was performed to bring the internal temperature to 70 ° C. Pressure is 5kg / cm while inserting propylene
Polymerization was carried out for 2 hours for 3 hours. Deactivate the catalyst with methanol,
It was washed with water to remove the catalyst residue, filtered and dried to obtain a powder. The powder obtained was 850 g and had an intrinsic viscosity of 1.78.
(Measured with a 135 ° C. tetralin solution), the boiling n-heptane extraction residual rate was 98.2% (extracted for 6 hours using a Kumagawa type extractor).
メチルフェニルジクロルシランとジメチルジクロルシラ
ンをトルエン中でナトリウムと反応してポリシラスチレ
ンを合成した(上述の文献の方法に準じた)。Methylphenyldichlorosilane and dimethyldichlorosilane were reacted with sodium in toluene to synthesize polysilastyrene (according to the method of the above-mentioned document).
上記ポリプロピレン100重量部に対してポリシラスチレ
ン0.1重量部を混合して溶融プレスをしてシート作り物
性を測定した。Sheet-forming physical properties were measured by mixing 0.1 part by weight of polysilastyrene with 100 parts by weight of the above polypropylene and performing melt pressing.
引っ張り降伏強さ(ASTM D638−67T)は365kg/cm2、曲
げ弾性率(ASTM D790−63)は21000kg/cm2、結晶化温度
(DSCを用い、10℃/minで降温して測定)は122.3℃であ
った。Tensile yield strength (ASTM D638-67T) is 365kg / cm 2 , flexural modulus (ASTM D790-63) is 21000kg / cm 2 , crystallization temperature (measured using DSC at 10 ℃ / min). It was 122.3 ° C.
比較例1 ポリシラスチレンを用いることなく成型して物性を測定
した他は実施例1と同様にしたところ、引っ張り降伏強
さ及び曲げ弾性率はそれぞれ330kg/cm2、18000kg/cm2で
あった。また、結晶化温度は112.5℃と低かった。When addition was measured molded to physical properties without using the Comparative Example 1 polysilastyrene were the same as in Example 1, the tensile yield strength and flexural modulus were respectively 330kg / cm 2, 18000kg / cm 2 . The crystallization temperature was low at 112.5 ° C.
実施例2、3 実施例1と同様にして得たポリジヘキシルシラン(実施
例2)、ポリメチルブチルシラン(実施例3)をそれぞ
れポリプロピレン100重量部に対して0.5重量部用いた他
は実施例1と同様にしたところ、それぞれ引っ張り降伏
強さは355kg/cm2、350kg/cm2であり、曲げ弾性率は2100
0kg/cm2、20500kg/cm2であった。また、結晶化温度は12
1.4℃および122.3℃であった。Examples 2 and 3 Examples in which 0.5 parts by weight of polydihexylsilane (Example 2) and polymethylbutylsilane (Example 3) obtained in the same manner as in Example 1 were used with respect to 100 parts by weight of polypropylene, respectively. 1 and was similarly, the tensile yield strength, respectively was 355kg / cm 2, 350kg / cm 2, the flexural modulus 2100
0kg / cm 2, it was 20500kg / cm 2. The crystallization temperature is 12
It was 1.4 ° C and 122.3 ° C.
本発明の組成物は物性に優れ工業的に極めて価値があ
る。The composition of the present invention has excellent physical properties and is extremely valuable industrially.
Claims (1)
り1個以上の炭化水素残基を有する有機ポリシランを含
有することを特徴とするポリプロピレン樹脂組成物。1. A polypropylene resin composition having a main chain of silicon and containing an organic polysilane having one or more hydrocarbon residues per silicon atom.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61250644A JPH0798879B2 (en) | 1986-10-23 | 1986-10-23 | Polypropylene resin composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61250644A JPH0798879B2 (en) | 1986-10-23 | 1986-10-23 | Polypropylene resin composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63105048A JPS63105048A (en) | 1988-05-10 |
| JPH0798879B2 true JPH0798879B2 (en) | 1995-10-25 |
Family
ID=17210924
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61250644A Expired - Lifetime JPH0798879B2 (en) | 1986-10-23 | 1986-10-23 | Polypropylene resin composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0798879B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH082999B2 (en) * | 1990-01-17 | 1996-01-17 | 信越化学工業株式会社 | Polyolefin composition |
| JP6484102B2 (en) * | 2015-04-28 | 2019-03-13 | 大阪ガスケミカル株式会社 | Crystal nucleating agent for polyolefin and its use |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5626939A (en) * | 1979-08-08 | 1981-03-16 | Sumitomo Naugatuck Co Ltd | Resin composition having excellent heat cycle characteristic |
-
1986
- 1986-10-23 JP JP61250644A patent/JPH0798879B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63105048A (en) | 1988-05-10 |
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