JPH08302050A - Production of polypropylene resin foam - Google Patents

Production of polypropylene resin foam

Info

Publication number
JPH08302050A
JPH08302050A JP10743295A JP10743295A JPH08302050A JP H08302050 A JPH08302050 A JP H08302050A JP 10743295 A JP10743295 A JP 10743295A JP 10743295 A JP10743295 A JP 10743295A JP H08302050 A JPH08302050 A JP H08302050A
Authority
JP
Japan
Prior art keywords
ethylene
propylene
weight
molecular weight
average molecular
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
Application number
JP10743295A
Other languages
Japanese (ja)
Other versions
JP3535259B2 (en
Inventor
Fusaaki Katou
房彰 加藤
Takashi Kamiebisu
孝 上夷
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.)
Tonen Chemical Corp
Original Assignee
Tonen Sekiyu Kagaku KK
Tonen Chemical Corp
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 Tonen Sekiyu Kagaku KK, Tonen Chemical Corp filed Critical Tonen Sekiyu Kagaku KK
Priority to JP10743295A priority Critical patent/JP3535259B2/en
Publication of JPH08302050A publication Critical patent/JPH08302050A/en
Application granted granted Critical
Publication of JP3535259B2 publication Critical patent/JP3535259B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE: To produce a polypropylene resin foam having a high content of fine and uniform closed cells and high rigidity with excellent moldability and high productivity by blending a specific ethylene-propylene block copolymer with a blowing agent and foaming the blend by extrusion. CONSTITUTION: This polypropylene resin foam is obtained by blending (A) an ethylene-propylene block copolymer having 1-10g/10 minutes melt flow rate, 1-10wt.% of ethylene content, >=6dl/g intrinsic viscosity [η] of p-xylene soluble content at 23 deg.C and the ratio of the weight-average molecular weight Mw/the number-average molecular weight Mn of >=10 with (B) a blowing agent (preferably a thermal decomposition type blowing agent such as azobisisobutyronitrile, etc.) in the ratio of preferably 0.1-30 pts.wt. of the component B based on 100 pts.wt. of the component A and foaming the blend by extrusion. The component A is preferably obtained by combining a process for polymerizing propylene in the presence of a stereospecific polymerization catalyst to give a crystalline propylene-based polymer with a process for copolymerizing propylene with ethylene to give a noncrystalline propylene-ethylene copolymer.

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、ポリプロピレン樹脂押
出発泡体の製造方法に関する。
FIELD OF THE INVENTION The present invention relates to a method for producing an extruded polypropylene resin foam.

【0002】[0002]

【従来の技術】ポリオレフィン系樹脂の押出発泡におい
ては、発泡に適正な粘弾性を持つ溶融状態で樹脂を発泡
させることが重量であり、樹脂の溶融粘度が高過ぎれば
発泡し難く、逆に低過ぎると発泡セルが破れてガスを樹
脂内に保持できなくなる。
2. Description of the Related Art In extrusion foaming of a polyolefin resin, it is important to foam the resin in a molten state having proper viscoelasticity for foaming. If the melt viscosity of the resin is too high, it is difficult to foam, and conversely low. If it passes, the foam cells will be broken and the gas cannot be retained in the resin.

【0003】結晶化度が高いポリプロピレン系樹脂は、
樹脂の粘弾性が僅かな温度変化により大きく変化し、発
泡適正温度範囲は非常に狭い。このような狭い温度範囲
内で押出発泡を行うことは非常に困難であり、該温度範
囲から外れた温度で得られた発泡体は、連続気泡構造に
なったり、全体が不均質な構造となったりする。
Polypropylene resin having high crystallinity is
The viscoelasticity of the resin changes greatly with a slight temperature change, and the appropriate foaming temperature range is very narrow. It is very difficult to carry out extrusion foaming within such a narrow temperature range, and a foam obtained at a temperature outside the temperature range has an open cell structure or an entirely inhomogeneous structure. Or

【0004】このため、従来ポリプロピレン系樹脂押出
発泡体製造に用いられる原料樹脂として、ポリプロピレ
ン系樹脂に、ポリプロピレン系樹脂よりも溶融張力の高
いポリエチレン系樹脂を混合したものが知られている
(特開平4−359034号公報)が、発泡安定性は確
保されるものの、得られる発泡体がポリプロピレン系樹
脂単独を用いて得られるものに比べ剛性、耐熱性が劣
り、従って発泡体の用途も制限されていた。
Therefore, as a raw material resin conventionally used for the production of extruded polypropylene-based resin foams, there is known a material in which a polypropylene-based resin is mixed with a polyethylene-based resin having a higher melt tension than that of the polypropylene-based resin (Japanese Patent Application Laid-Open No. Hei 10 (1999) -242242). No. 4-359034), the foaming stability is ensured, but the resulting foam is inferior in rigidity and heat resistance to that obtained by using a polypropylene resin alone, and therefore the use of the foam is limited. It was

【0005】又、2種類のエチレン−プロピレンブロッ
ク共重合体を原料樹脂とすることも提案されている(特
開昭63−288731号公報)が、この場合、得られ
る発泡体は、剛性、耐熱性には問題がないが、内部構造
が均質でなく、衝撃強度が劣るという問題があった。
It has also been proposed to use two kinds of ethylene-propylene block copolymers as raw materials (Japanese Patent Laid-Open No. 63-288731). In this case, the resulting foam has rigidity and heat resistance. Although there is no problem with the property, there was a problem that the internal structure was not uniform and the impact strength was poor.

【0006】[0006]

【発明が解決しようとする課題】本発明は、ポリプロピ
レン系樹脂の本来の剛性、耐熱性を維持し、微細で均質
な内部構造を有するポリプロピレン樹脂押出発泡体を製
造する方法を提供することを目的とする。
SUMMARY OF THE INVENTION It is an object of the present invention to provide a method for producing a polypropylene resin extruded foam having a fine and uniform internal structure while maintaining the original rigidity and heat resistance of the polypropylene resin. And

【0007】[0007]

【課題を解決するための手段】本発明者らは、鋭意研究
を行った結果、特定のエチレン−プロピレン共重合体を
原料として用い、押出発泡することにより本発明の目的
が達成し得ることを見出して、本発明を完成した。
As a result of intensive studies, the inventors of the present invention have found that the object of the present invention can be achieved by extrusion foaming using a specific ethylene-propylene copolymer as a raw material. Found and completed the present invention.

【0008】すなわち、本発明は、メルトフローレイト
が1〜10g/10分、エチレン含有量が1〜10重量
%、23℃のパラキシレン可溶分の固有粘度[η]が6
dl/g以上、重量平均分子量(Mw)と数平均分子量
(Mn)との比Mw/Mnが10以上であるエチレン−
プロピレンブロック共重合体と発泡剤とを混合し押出発
泡させることを特徴とするポリプロピレン樹脂発泡体の
製造方法を要旨とする。
That is, according to the present invention, the melt flow rate is 1 to 10 g / 10 minutes, the ethylene content is 1 to 10% by weight, and the intrinsic viscosity [η] of the paraxylene soluble matter at 23 ° C. is 6%.
ethylene having a dl / g or more and a ratio Mw / Mn of the weight average molecular weight (Mw) to the number average molecular weight (Mn) of 10 or more;
A gist is a method for producing a polypropylene resin foam, which comprises mixing a propylene block copolymer and a foaming agent and subjecting the mixture to extrusion foaming.

【0009】本発明で用いられるエチレン−プロピレン
ブロック共重合体(以下、EPBCということがあ
る。)は、メルトフローレイト(MFR;JIS K7
210;荷重2.16kg,230℃で測定)が1〜1
0g/10分、好ましくは2〜7g/10分であり、エ
チレン含有量が1〜10重量%、好ましくは2〜7g重
量%であり、23℃のパラキシレン可溶分の固有粘度
[η](135℃のテトラリン中で測定)が6dl/g
以上、好ましくは6〜8dl/gであり、重量平均分子
量(Mw)と数平均分子量(Mn)との比(Mw/M
n)が10以上、好ましくは12〜15である。
The ethylene-propylene block copolymer (hereinafter sometimes referred to as EPBC) used in the present invention has a melt flow rate (MFR; JIS K7).
210; load 2.16 kg, measured at 230 ° C) is 1 to 1
0 g / 10 minutes, preferably 2 to 7 g / 10 minutes, ethylene content 1 to 10% by weight, preferably 2 to 7 g% by weight, and the intrinsic viscosity [η] of the para-xylene-soluble component at 23 ° C. (Measured in tetralin at 135 ° C) is 6 dl / g
The above is preferably 6 to 8 dl / g, and the ratio (Mw / M) of the weight average molecular weight (Mw) to the number average molecular weight (Mn).
n) is 10 or more, preferably 12 to 15.

【0010】EPBCのMFRがメルトフローレイトが
1g/10分未満では、押出性が困難となり、10g/
10分を超えると発泡成形性が悪化する。
If the melt flow rate of EPBC MFR is less than 1 g / 10 min, the extrudability becomes difficult and the melt flow rate becomes 10 g / min.
If it exceeds 10 minutes, the foam moldability deteriorates.

【0011】EPBCのエチレン含有量が1重量%未満
では、発泡体の衝撃強度が不足し、10重量%を超える
と、発泡体の剛性が不足する。
When the ethylene content of EPBC is less than 1% by weight, the impact strength of the foam is insufficient, and when it exceeds 10% by weight, the rigidity of the foam is insufficient.

【0012】EPBCの23℃のパラキシレン可溶分
(CXS)の[η]が6dl/g未満では、発泡体中の
独立気泡径が粗大となり、衝撃強度が低下する。
If the [η] of the para-xylene-soluble component (CXS) at 23 ° C. of EPBC is less than 6 dl / g, the diameter of the closed cells in the foam becomes large and the impact strength decreases.

【0013】EPBCのMw/Mnが10未満では、樹
脂の流動性が悪化し、これにより押出成形時の樹脂吐出
量が低下し、充分な生産量が得られない。
When the Mw / Mn of EPBC is less than 10, the fluidity of the resin is deteriorated, which reduces the amount of resin discharged during extrusion molding, and a sufficient amount of production cannot be obtained.

【0014】このようなEPBCは、チーグラー・ナッ
タ型触媒の存在下、プロピレンとエチレンをブロック共
重合することにより製造することができる。より詳細に
は、立体特異性重合触媒の存在下、プロピレンを重合し
て結晶性プロピレン系重合体を得る工程と、プロピレン
とエチレンを共重合させ上記CXS部分に相当する非晶
性プロピレン−エチレン共重合体を得る工程で組み合わ
せることにより得られる。
Such EPBC can be produced by block-copolymerizing propylene and ethylene in the presence of a Ziegler-Natta type catalyst. More specifically, in the presence of a stereospecific polymerization catalyst, a step of polymerizing propylene to obtain a crystalline propylene-based polymer, and a step of copolymerizing propylene and ethylene to obtain an amorphous propylene-ethylene copolymer corresponding to the CXS portion are described. It is obtained by combining in the process of obtaining a polymer.

【0015】これらの工程の前後関係は、特に規定され
ないが、後工程は、前工程で得られた重合体及び用いら
れた重合触媒の存在下、引き続き行われる。特に、非晶
性プロピレン−エチレン共重合体を得る工程は、[η]
が6dl/g以上という高分子量の共重合体を製造する
必要上、分子量調節剤である水素が実質存在しない条件
下で行うのが肝要である。上記EPBC中の上記CXS
部分の割合は、通常5〜50重量%、好ましくは10〜
30重量%である。
The order of these steps is not particularly limited, but the post-step is continuously carried out in the presence of the polymer obtained in the pre-step and the polymerization catalyst used. In particular, the step of obtaining an amorphous propylene-ethylene copolymer is [η]
In order to produce a high molecular weight copolymer having a molecular weight of 6 dl / g or more, it is important to carry out under the condition that hydrogen, which is a molecular weight regulator, does not substantially exist. The CXS in the EPBC
The proportion of the portion is usually 5 to 50% by weight, preferably 10 to
It is 30% by weight.

【0016】本発明は、上記EPBCと発泡剤とを混合
し押出発泡するものであるが、EPBCは、押出発泡の
前に、必要に応じて無機充填剤、酸化防止剤、紫外線吸
収剤、光安定剤、着色剤等の添加剤を添加することがで
きる。
In the present invention, the above EPBC and a foaming agent are mixed and extruded and foamed. In EPBC, before the extrusion and foaming, an inorganic filler, an antioxidant, an ultraviolet absorber, a light absorber are added, if necessary. Additives such as stabilizers and colorants can be added.

【0017】発泡剤としては、プロパン、ブタン、ペン
タン等の低級脂肪族炭化水素、シクロブタン、シクロペ
ンタン等の低級脂環式炭化水素及びモノクロロジフルオ
ロメタン、ジクロロジフルオロメタン、トリクロロジフ
ルオロエタン、トリクロロトリフルオロエタン、ジクロ
ロテトラフルオロエタン、メチルクロライド、エチルク
ロライド、メチレンクロライド等のハロゲン化炭化水素
からなる揮発型発泡剤、窒素、炭酸ガス、酸素、空気等
のガス状発泡剤、重炭酸ソーダ、重炭酸アンモニウム、
ジニトロソペンタメチレンテトラミン、トルエンスルホ
ニルヒトラジド、アゾジカルボンアミド、p,p′−オ
キシビスベンゼンスルホニルヒドラジド、アゾビスイソ
ブチロニトリル等からなる熱分解型発泡剤等が用いられ
る。これらの中でも、特に熱分解型発泡剤が望ましい。
Examples of the blowing agent include lower aliphatic hydrocarbons such as propane, butane and pentane, lower alicyclic hydrocarbons such as cyclobutane and cyclopentane, and monochlorodifluoromethane, dichlorodifluoromethane, trichlorodifluoroethane, trichlorotrifluoroethane, Volatile foaming agents consisting of halogenated hydrocarbons such as dichlorotetrafluoroethane, methyl chloride, ethyl chloride, methylene chloride, gaseous foaming agents such as nitrogen, carbon dioxide, oxygen, air, sodium bicarbonate, ammonium bicarbonate,
A thermally decomposable foaming agent made of dinitrosopentamethylenetetramine, toluenesulfonyl human azide, azodicarbonamide, p, p'-oxybisbenzenesulfonyl hydrazide, azobisisobutyronitrile or the like is used. Among these, the thermal decomposition type foaming agent is particularly desirable.

【0018】これらの発泡剤の使用量は、EPBC10
0重量部当り、0.1〜30重量部である。
The amount of these foaming agents used is EPBC10.
It is 0.1 to 30 parts by weight per 0 parts by weight.

【0019】上記EPBCと発泡剤の混合は、望ましく
は、押出機等の内部でEPBCの溶融下、両者を混練す
ることにより行われるが、発泡剤は、熱分解型発泡剤の
場合、EPBCを押出機等に供給する前に、EPBCと
予め混合して、或いはEPBCとは別々に、押出機等に
供給してもよく、又、揮発型発泡剤やガス状発泡剤の場
合、例えばベント式押出し機等のスクリュー中間部から
溶融したEPBC中に圧入してよい。
Mixing of the EPBC and the foaming agent is preferably carried out by kneading the EPBC inside an extruder or the like while melting the EPBC. In the case of a pyrolytic foaming agent, the EPBC is mixed with the EPBC. Before being supplied to the extruder or the like, it may be mixed with EPBC in advance or separately from the EPBC, and may be supplied to the extruder or the like. In the case of a volatile type foaming agent or a gaseous foaming agent, for example, a vent type It may be pressed into the melted EPBC from the middle part of the screw of an extruder or the like.

【0020】押出機等で混練された上記EPBCと発泡
剤は、押出機先端に取付けられたダイスを通して、押出
発泡される。発泡倍率は1.5〜6倍、好ましくは2〜
5倍である。得られる発泡体の形状は、任意であり、例
えばフィルム状、シート状、パイプ状、円筒状等が挙げ
られる。
The EPBC and foaming agent kneaded by an extruder or the like are extruded and foamed through a die attached to the tip of the extruder. The expansion ratio is 1.5 to 6 times, preferably 2 to
5 times. The shape of the obtained foam is arbitrary, and examples thereof include a film shape, a sheet shape, a pipe shape, and a cylindrical shape.

【0021】[0021]

【実施例】以下、本発明を実施例により詳細に説明す
る。例における%(パーセント)は重量基準である。
EXAMPLES The present invention will be described in detail below with reference to examples. Percentages in the examples are by weight.

【0022】なお、原料樹脂及び得られた発泡体の物性
の測定は、下記の方法により行った。
The physical properties of the raw material resin and the obtained foam were measured by the following methods.

【0023】独立気泡率 幅方向に切断した発泡シート断面の写真を画像解析によ
り、全気泡に対する独立気泡の割合を算出した。
Closed cell ratio The ratio of the closed cells to all the cells was calculated by analyzing the photograph of the cross section of the foamed sheet cut in the width direction.

【0024】平均独立気泡径 独立気泡率算出のときと同様にして得た写真を画像解析
により、独立した気泡の直径を測定し、その平均径を算
出した。
Average Closed Cell Diameter A photograph obtained in the same manner as in the calculation of the closed cell ratio was subjected to image analysis to measure the diameter of the independent bubbles, and the average diameter was calculated.

【0025】独立気泡径分率 全独立気泡に対する気泡径が平均独立気泡径±5μmの
範囲の独立気泡の割合を算出した。
The bubble diameter to the closed cell diameter ratio all closed cells was calculated the ratio of closed cells in the range of the average closed cell diameter ± 5 [mu] m.

【0026】ドローダウン速度 原料樹脂から成形した厚さ0.5mmのシートから、3
0mm×300mmの短冊片を切り取り、治具に固定
後、175℃のエアーオーブン中で加熱し、シートが溶
融後、垂れる速度を測定。
Drawdown speed From a 0.5 mm-thick sheet molded from raw material resin, 3
Cut a strip of 0 mm x 300 mm, fix it to a jig, heat it in an air oven at 175 ° C, and measure the rate of sagging after the sheet has melted.

【0027】デュポン衝撃強度 JIS K7211に準拠、測定温度23℃。 DuPont impact strength Measured at 23 ° C. according to JIS K7211.

【0028】(実施例1)エチレン含有量10%、メル
トフローレイト(MFR)2.0g/10分、23℃の
パラキシレン可溶分が20%でその固有粘度[η]8.
0dl/g、重量平均分子量(Mw)と数平均分子量
(Mn)との比(Mw/Mn)13のエチレン−プロピ
レンブロック共重合体(EPBC)100重量部とアゾ
ジカルボンアミド1重量部を予めドライブレンドした
後、押出機(50mmφ,L/D28)に供給し、この
押出機に装着されたTダイ(樹脂通路,幅500mm,
高さ1.5mm)から180℃で樹脂を吐出して、発泡
倍率2.0倍、厚さ3mmの発泡シートを成形した。
Example 1 Ethylene content 10%, melt flow rate (MFR) 2.0 g / 10 min, paraxylene solubles at 23 ° C. 20% and its intrinsic viscosity [η] 8.
100 parts by weight of ethylene-propylene block copolymer (EPBC) having 0 dl / g and a ratio (Mw / Mn) of weight average molecular weight (Mw) to number average molecular weight (Mn) of 13 and 1 part by weight of azodicarbonamide were dried in advance. After blending, the mixture was supplied to an extruder (50 mmφ, L / D28), and the T die (resin passage, width 500 mm,) attached to this extruder was used.
The resin was discharged from a height of 1.5 mm) at 180 ° C. to form a foam sheet having a foaming ratio of 2.0 and a thickness of 3 mm.

【0029】用いたEPBC樹脂のドローダウン速度
は、1.0mm/秒であり、樹脂の吐出量は35kg/
時間であった。得られた発泡シートの物性等は表1の通
りであった。
The EPBC resin used had a drawdown speed of 1.0 mm / sec and a resin discharge rate of 35 kg / sec.
It was time. The physical properties and the like of the obtained foamed sheet are as shown in Table 1.

【0030】(実施例2〜4)EPBCとして、表1に
示す性状のものを用いた以外は、実施例1と同様にして
発泡シートを得た。各実施例のドローダウン速度、樹脂
の吐出量、発泡シートの物性等は表1の通りであった。
(Examples 2 to 4) Foamed sheets were obtained in the same manner as in Example 1 except that the EPBCs having the properties shown in Table 1 were used. Table 1 shows the drawdown speed, the discharge amount of the resin, the physical properties of the foamed sheet, and the like in each example.

【0031】(比較例1〜6)EPBCとして、表1に
示す性状のものを用いた以外は、実施例1と同様にして
発泡シートを得た。なお、比較例6で用いたEPBC
は、比較例2で用いたEPBC(50重量部)と比較例
3で用いたEPBC(50重量部)との混合物である。
(Comparative Examples 1 to 6) Foamed sheets were obtained in the same manner as in Example 1 except that EPBCs having the properties shown in Table 1 were used. The EPBC used in Comparative Example 6
Is a mixture of EPBC (50 parts by weight) used in Comparative Example 2 and EPBC (50 parts by weight) used in Comparative Example 3.

【0032】各比較例の樹脂のドローダウン速度、樹脂
の吐出量、発泡シートの物性等は表1の通りであった、
The drawdown speed of the resin of each comparative example, the discharge amount of the resin, the physical properties of the foamed sheet and the like are shown in Table 1.

【表1】 表1から明らかなように、本発明に係る特定のEPBC
を原料樹脂として用いて発泡体を製造すると、耐衝撃性
が大きく、かつ独立気泡率が高く、微細(平均独立気泡
径が小さい)で、均質(独立気泡径分率が高い)な発泡
体が、成形性良く(ドローダウン速度が1.5mm/秒
以下)、かつ高生産性(吐出量が大)で製造できること
が判る。
[Table 1] As is apparent from Table 1, the specific EPBC according to the present invention
When a foam is produced by using as a raw material resin, a foam having a high impact resistance, a high closed cell ratio, a fine (small average closed cell diameter) and a homogeneous (high closed cell diameter fraction) is obtained. It can be seen that it can be manufactured with good moldability (drawdown speed of 1.5 mm / sec or less) and high productivity (large discharge amount).

【0033】[0033]

【発明の効果】微細、均質の独立気泡の含有量が高く、
かつ高剛性のポリプロピレン系樹脂押出発泡体が成形性
良く、高い生産性で製造することができる。
The content of fine and homogeneous closed cells is high,
In addition, a highly rigid polypropylene resin extruded foam can be manufactured with good moldability and high productivity.

【0034】このような発泡体は、自動車、家電、建
材、食品容器、文具、雑貨用等の多くの部材として、好
適に使用することができる。
Such a foam can be suitably used as many members for automobiles, home appliances, building materials, food containers, stationery, miscellaneous goods, and the like.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 メルトフローレイトが1〜10g/10
分、エチレン含有量が1〜10重量%、23℃のパラキ
シレン可溶分の固有粘度[η]が6dl/g以上、重量
平均分子量(Mw)と数平均分子量(Mn)との比Mw
/Mnが10以上であるエチレン−プロピレンブロック
共重合体と発泡剤とを混合し押出発泡させることを特徴
とするるポリプロピレン樹脂発泡体の製造方法。
1. A melt flow rate of 1 to 10 g / 10.
Min, ethylene content is 1 to 10% by weight, the intrinsic viscosity [η] of the para-xylene soluble component at 23 ° C. is 6 dl / g or more, and the ratio Mw of the weight average molecular weight (Mw) and the number average molecular weight (Mn).
A method for producing a polypropylene resin foam, which comprises mixing an ethylene-propylene block copolymer having a Mn of 10 or more and a foaming agent and subjecting the mixture to extrusion foaming.
【請求項2】 メルトフローレイトが2〜7g/10
分、エチレン含有量が2〜7重量%、23℃のパラキシ
レン可溶分の固有粘度[η]が6〜8dl/g、重量平
均分子量(Mw)と数平均分子量(Mn)との比Mw/
Mnが12〜15であるエチレン−プロピレンブロック
共重合体と発泡剤とを混合し押出発泡させることを特徴
とするるポリプロピレン樹脂発泡体の製造方法。
2. The melt flow rate is 2 to 7 g / 10.
, Ethylene content of 2 to 7% by weight, intrinsic viscosity [η] of the para-xylene soluble matter at 23 ° C. of 6 to 8 dl / g, ratio Mw of weight average molecular weight (Mw) and number average molecular weight (Mn). /
A method for producing a polypropylene resin foam, which comprises mixing an ethylene-propylene block copolymer having an Mn of 12 to 15 and a foaming agent and subjecting the mixture to extrusion foaming.
JP10743295A 1995-05-01 1995-05-01 Method for producing polypropylene resin foam Expired - Lifetime JP3535259B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10743295A JP3535259B2 (en) 1995-05-01 1995-05-01 Method for producing polypropylene resin foam

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10743295A JP3535259B2 (en) 1995-05-01 1995-05-01 Method for producing polypropylene resin foam

Publications (2)

Publication Number Publication Date
JPH08302050A true JPH08302050A (en) 1996-11-19
JP3535259B2 JP3535259B2 (en) 2004-06-07

Family

ID=14458999

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10743295A Expired - Lifetime JP3535259B2 (en) 1995-05-01 1995-05-01 Method for producing polypropylene resin foam

Country Status (1)

Country Link
JP (1) JP3535259B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012025858A (en) * 2010-07-23 2012-02-09 Cp Kasei Kk Foamed sheet made of propylene-based resin

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012025858A (en) * 2010-07-23 2012-02-09 Cp Kasei Kk Foamed sheet made of propylene-based resin

Also Published As

Publication number Publication date
JP3535259B2 (en) 2004-06-07

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