JPS5958049A - Polyolefin resin composition - Google Patents
Polyolefin resin compositionInfo
- Publication number
- JPS5958049A JPS5958049A JP16936382A JP16936382A JPS5958049A JP S5958049 A JPS5958049 A JP S5958049A JP 16936382 A JP16936382 A JP 16936382A JP 16936382 A JP16936382 A JP 16936382A JP S5958049 A JPS5958049 A JP S5958049A
- Authority
- JP
- Japan
- Prior art keywords
- ethylene
- propylene
- resin composition
- density polyethylene
- mixture
- 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.)
- Granted
Links
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、真空成形性及び引張り伸び性1こ優れるポリ
オレフィン樹脂Jこ関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polyolefin resin J having excellent vacuum formability and tensile elongation properties.
従来、ポリプロピレン樹脂は優れた特性を持ちながら、
その真空成形時における垂れ下りの大きさから真空成形
性か悪く、その改良策としてポリエチレンをブレンドす
る手法か用いられている。しかし、ポリエチレンの添加
■か少ないと十分な真空成形性か得られず、一方真空成
形性か良好になるように添加量を多くすると引張り伸び
率か低下してポリプロピレン本来の特性を損う欠点を有
している。Conventionally, polypropylene resin has excellent properties, but
Vacuum formability is poor due to the amount of sagging during vacuum forming, and as an improvement measure a method of blending polyethylene is used. However, if polyethylene is added too little, sufficient vacuum formability cannot be obtained, while if the amount added is increased to improve vacuum formability, the tensile elongation rate decreases, impairing the inherent properties of polypropylene. have.
本発明は、かかる欠点を改良すべく研究の結果、エチレ
ンープロピレンブロンク共m合体!!独もしくはこれと
ポリプロピレン単独重合体との混合物に、溶融粘度と溶
融張力の比か大きい高密度ポリエチレンを添加する事に
より、ポリプロピレンとポリエチレンの相溶性を高め真
空成形性に優れかつ引張り伸び性に優れるポリオレフィ
ン樹脂組成物を得る事を見出した。As a result of research to improve these drawbacks, the present invention has been developed by combining ethylene-propylene bronc! ! By adding high-density polyethylene, which has a large ratio of melt viscosity to melt tension, to a mixture of polypropylene and a polypropylene homopolymer, the compatibility between polypropylene and polyethylene is increased, resulting in excellent vacuum formability and tensile elongation. It has been found that a polyolefin resin composition can be obtained.
すなわち、エチレンープロピレンブロソク共重合体単独
もしくはこれとポリプロピレン単独重合体との混合物6
0〜80重伍係と190℃シェアレート5SeC−’に
おける溶融粘度と溶融張力の比か3X10A−5XIO
’ボイズ/ g rなる高密度ポリエチレン20〜40
重fa %を配合する事を特徴とする。本発明1こ用い
るポリプロピレンは、エチレン−プロピレンプロ・ツク
共重合体単独てもよいし、これとポリプロピレン単独重
合体との混合物でもよくその混合比も自由であるか、X
空成形時の加熱による垂れ下がりを少なくする為lこ2
30℃におけるメルトフローレート(MFR)か1 g
r / I Q m i n以下か好ましい。また1
本発明に用いる高密度ポリエチレンは、190℃シェア
レート6sec−’での溶融粘度/溶融張力の1直か3
×10′ボイズ/ g rに達しないと樹脂組成物の引
張り伸び性は低く、5×104 ボイズ/ g r以
上になると真空成形加熱時の垂れ下がりが大きくなって
真空成形性を損なうので好1しくない。さらに、高密度
ポリエチレンの配合量か増すと真空成形性は向上するか
耐熱性は低下し、配合量か少ないと真空成形性か悪くな
る為lこ好適な添加凰は20〜40重111%である。That is, the ethylene-propylene broth copolymer alone or a mixture of this and a polypropylene homopolymer 6
Ratio of melt viscosity and melt tension at 0 to 80 weight ratio and 190℃ shear rate 5SeC-'3X10A-5XIO
'Boys/gr high density polyethylene 20~40
It is characterized by containing a heavy fa%. Invention 1 The polypropylene used in this invention may be an ethylene-propylene pro-tox copolymer alone, or a mixture of this and a polypropylene homopolymer, and the mixing ratio may be arbitrary.
To reduce sagging due to heating during air molding,
Melt flow rate (MFR) at 30°C or 1 g
r/I Q min or less is preferable. Also 1
The high-density polyethylene used in the present invention has a melt viscosity/melt tension ratio of 1 or 3 at a shear rate of 6 sec-' at 190°C.
If the tensile extensibility of the resin composition does not reach x10' voids/gr, it is low, and if it exceeds 5 x 104 voids/gr, the sagging during heating for vacuum forming becomes large and the vacuum formability is impaired, so this is preferable. do not have. Furthermore, if the amount of high-density polyethylene blended increases, the vacuum formability will improve or the heat resistance will decrease, and if the blended amount is small, the vacuum formability will deteriorate. be.
次1こ1本発明の詳細な説明する。Next, the present invention will be explained in detail.
実施例】 エチレン−プロピレンブロックJCff1合体。Example】 Ethylene-propylene block JCff1 combination.
(MpR=o、s)を30重量%、ポリプロピレン単独
重合体(MFR=0.5)を30重量%、溶融粘度/溶
融張力の直か4 X 10’°ボイズ/ g rである
高密度ポリエチレン(MFR−03)を40重量qII
配合して樹脂組成物を得り。コれを40喘φ押出m (
L/D=26. CR=30)にて板状に成形し、真空
成形時の垂れ下り量及び引張り伸び率を測定した。結果
を第1表1こ示す。(MpR = o, s), 30% by weight of polypropylene homopolymer (MFR = 0.5), high-density polyethylene with a melt viscosity/melt tension of 4 X 10'° voids/g r (MFR-03) at 40 weight qII
Blend to obtain a resin composition. Extrude this to 40 mmφ (
L/D=26. CR=30), and the amount of sagging and tensile elongation during vacuum forming were measured. The results are shown in Table 1.
実施例2
実施例1と同様のエチレン−プロピレンブロック共重合
体を60重1L高密度ポリエチレンを40重ffi%配
合して樹脂組成物を得た。これを同様に板状に成形し、
真空成形時の垂れ下り量及び引張り伸び率を測定した。Example 2 A resin composition was obtained by blending the same ethylene-propylene block copolymer as in Example 1 with 40 wt ffi% of 60 wt 1 L high-density polyethylene. Form this into a plate shape in the same way,
The amount of sagging and tensile elongation during vacuum forming were measured.
結果を第1表に示す。The results are shown in Table 1.
比較例1
実施例1と同様のエチレン−プロピレンブロック共重合
体を50重量%、ポリプロピレン単独重合体を50重量
係配合して樹脂組成物を得た。Comparative Example 1 A resin composition was obtained by blending 50% by weight of the same ethylene-propylene block copolymer as in Example 1 and 50% by weight of a polypropylene homopolymer.
比較例2
実施例1と同様のエチレンーブロビレンプロソク共重合
体を30重短係、ポリプロピレン単独重合体を30重f
fi%、溶融粘度/溶融張力の値か2XIO’ボイズ/
g rの高密度ポリエチレン(MFR=03)を4o
重ffi%配合して樹脂組成物を得た。Comparative Example 2 The same ethylene-propylene copolymer as in Example 1 was used in a 30-fold ratio, and the polypropylene homopolymer was used in a 30-fold ratio.
fi%, melt viscosity/melt tension value or 2XIO'voise/
gr high density polyethylene (MFR=03)
A resin composition was obtained by blending the resin composition with heavy ffi%.
比較例3
実施例1と同様のエチレン−プロピレンブロック共重合
体を60重量係、比較例2と同様の高密度ポリエチレン
を40重量係配合して樹脂組成物を得た。Comparative Example 3 A resin composition was obtained by blending the same ethylene-propylene block copolymer as in Example 1 at 60 weight percent and the same high-density polyethylene as in Comparative Example 2 at 40 weight percent.
以上の比較例の樹脂組成物を同様に板状に成形し、真空
成形時の垂れ下り量及び引張り伸び率を測定した結果を
第1表に示す。The resin compositions of the above comparative examples were similarly molded into plate shapes, and the amount of sag and tensile elongation during vacuum forming were measured. Table 1 shows the results.
比較例4
実施例】と同様のエチレンープロピレンブロソク共重合
体を板状1こ成形し、真空成形時の垂れ下り徂及び引張
り伸び率の測定結果を第1表に示す。Comparative Example 4 The same ethylene-propylene broth copolymer as in Example was molded into a single plate, and Table 1 shows the measurement results of the sag width and tensile elongation during vacuum molding.
第 1 表
第1表から明らかなよう1こ1本発明は真空成形時の加
熱によるシートの垂れ下りか減少する結果、真空成形性
か良くなり大面積での真空成形か容易1こなる。甘だ、
引張り伸び性かよくポリプロピレン本来の特性を損なう
ことなく真空成形性の改良か図れる点1本発明の工業的
偏置は極めて大なるものである。Table 1 As is clear from Table 1, the present invention reduces the sagging of the sheet due to heating during vacuum forming, resulting in improved vacuum formability and easy vacuum forming of large areas. It's sweet.
The industrial application of the present invention is extremely large in that it has good tensile elongation and can improve vacuum formability without impairing the inherent properties of polypropylene.
特許出願人patent applicant
Claims (1)
れとポリプロピレン単独重合体との混合物60〜80重
ffi%と、190℃シェアレー ) 6sec””’
におりる溶融粘度と溶融張力の比か3Xl O’〜5X
lO’ボイズ/ g rである高密度ポリエチレン20
〜40重量係を配合してなることを特徴とするポリオレ
フィン樹脂組成物。60 to 80% by weight of ethylene-propylene broth copolymer alone or a mixture of this and polypropylene homopolymer, and a shear rate of 190° C.) 6 sec""'
The ratio of melt viscosity and melt tension is 3Xl O'~5X
High-density polyethylene with lO'boys/gr 20
A polyolefin resin composition characterized in that it contains a polyolefin resin composition of .about.40% by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16936382A JPS5958049A (en) | 1982-09-28 | 1982-09-28 | Polyolefin resin composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16936382A JPS5958049A (en) | 1982-09-28 | 1982-09-28 | Polyolefin resin composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5958049A true JPS5958049A (en) | 1984-04-03 |
JPS643903B2 JPS643903B2 (en) | 1989-01-24 |
Family
ID=15885187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16936382A Granted JPS5958049A (en) | 1982-09-28 | 1982-09-28 | Polyolefin resin composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5958049A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59232134A (en) * | 1983-06-16 | 1984-12-26 | Idemitsu Petrochem Co Ltd | Ethylene polymer composition |
CN106939098A (en) * | 2016-01-04 | 2017-07-11 | 韩华道达尔有限公司 | Polypropylene resin composite and the product prepared using it |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4982200A (en) * | 1972-12-12 | 1974-08-07 | ||
JPS52121657A (en) * | 1976-04-07 | 1977-10-13 | Sumitomo Chem Co Ltd | Polypropylene composition |
JPS5558245A (en) * | 1978-10-19 | 1980-04-30 | Sumitomo Chem Co Ltd | Polyolefin resin composition |
JPS5672042A (en) * | 1979-11-16 | 1981-06-16 | Sumitomo Chem Co Ltd | Polyolefin resin composition |
JPS56141343A (en) * | 1980-04-05 | 1981-11-05 | Mitsubishi Chem Ind Ltd | Polyolefin composition |
-
1982
- 1982-09-28 JP JP16936382A patent/JPS5958049A/en active Granted
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4982200A (en) * | 1972-12-12 | 1974-08-07 | ||
JPS52121657A (en) * | 1976-04-07 | 1977-10-13 | Sumitomo Chem Co Ltd | Polypropylene composition |
JPS5558245A (en) * | 1978-10-19 | 1980-04-30 | Sumitomo Chem Co Ltd | Polyolefin resin composition |
JPS5672042A (en) * | 1979-11-16 | 1981-06-16 | Sumitomo Chem Co Ltd | Polyolefin resin composition |
JPS56141343A (en) * | 1980-04-05 | 1981-11-05 | Mitsubishi Chem Ind Ltd | Polyolefin composition |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59232134A (en) * | 1983-06-16 | 1984-12-26 | Idemitsu Petrochem Co Ltd | Ethylene polymer composition |
CN106939098A (en) * | 2016-01-04 | 2017-07-11 | 韩华道达尔有限公司 | Polypropylene resin composite and the product prepared using it |
CN106939098B (en) * | 2016-01-04 | 2019-09-13 | 韩华道达尔有限公司 | Polypropylene resin composite and the product prepared using it |
Also Published As
Publication number | Publication date |
---|---|
JPS643903B2 (en) | 1989-01-24 |
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