JPS5876228A - Polypropylene synthetic resin foamed and molded body - Google Patents

Polypropylene synthetic resin foamed and molded body

Info

Publication number
JPS5876228A
JPS5876228A JP56175991A JP17599181A JPS5876228A JP S5876228 A JPS5876228 A JP S5876228A JP 56175991 A JP56175991 A JP 56175991A JP 17599181 A JP17599181 A JP 17599181A JP S5876228 A JPS5876228 A JP S5876228A
Authority
JP
Japan
Prior art keywords
particles
synthetic resin
density
closed
mold
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
JP56175991A
Other languages
Japanese (ja)
Other versions
JPH0139335B2 (en
Inventor
Kuninori Hirozawa
広沢 邦則
Hideki Kuwabara
英樹 桑原
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.)
JSP Corp
Original Assignee
JSP 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 JSP Corp filed Critical JSP Corp
Priority to JP56175991A priority Critical patent/JPS5876228A/en
Publication of JPS5876228A publication Critical patent/JPS5876228A/en
Publication of JPH0139335B2 publication Critical patent/JPH0139335B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/36Feeding the material to be shaped
    • B29C44/38Feeding the material to be shaped into a closed space, i.e. to make articles of definite length
    • B29C44/44Feeding the material to be shaped into a closed space, i.e. to make articles of definite length in solid form
    • B29C44/445Feeding the material to be shaped into a closed space, i.e. to make articles of definite length in solid form in the form of expandable granules, particles or beads
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C44/00Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
    • B29C44/34Auxiliary operations
    • B29C44/3415Heating or cooling
    • B29C44/3426Heating by introducing steam in the mould
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2023/00Use of polyalkenes or derivatives thereof as moulding material
    • B29K2023/10Polymers of propylene
    • B29K2023/12PP, i.e. polypropylene

Abstract

PURPOSE:To improve the mechanical strength, by fillig a mold, which can be closed, but not be tightly closed, with polypropylene resin prefoamed particles, and heating the prefoamed particles to be molded into a body having a density of 0.06-0.3g/cm<3>, and a cell membrane thickness of 1-50mu. CONSTITUTION:The prefoamd particles are produced by incorporating 5- 30pts.wt. volatile foaming agent into 100pts.wt. polymer such as ethylene/propylene random copolymer, propylene monopolymer, etc. As said volatile foaming agent, aliphatic hydrocarbons such as propane, butane, etc. and cycloaliphatic hydrocarbons such as cyclobutane, etc. can be used. The prefoamed particles are matured at normal temperature under normal pressure, and then are matured under pressure to be provided with an internal pressure of 0.3-5kg/cm<2>G, and the mold, which can be closed, but not be tightly closed, is filled with the prefoamed particles, and the preforamed particles are heated and expanded using steam of 2-5kg/cm<2>G to obtain a molded body having a density of 0.06-0.3g/ cm<3>, and a cell membrane thickness of 1-50mu.

Description

【発明の詳細な説明】 本発明はポリプロピレン系合成樹脂発泡成型体に関する
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polypropylene synthetic resin foam molded article.

予備発泡粒子を、閉鎖し得るが密閉し得ない型に充填し
、加熱して前記粒子を発泡させて得られる成型体は知ら
れており、いわゆるビーズ成m品はそれ自身の有する特
性によって緩mm、包装材。
Molded products obtained by filling pre-expanded particles into a mold that can be closed but not sealed and heated to foam the particles are known. mm, packaging material.

断熱材、建築資材等に利用されており、@に高密度発泡
体の場合は2重量物の包装材、構造材、建材、車輌部材
等の比較的大きい機械的強度が要求されるものに対する
用適が見込まれている。従来。
It is used for insulation materials, construction materials, etc., and in the case of @high-density foam, it is used for packaging materials for heavy items, structural materials, building materials, vehicle components, etc. that require relatively high mechanical strength. expected to be suitable. Conventional.

発泡成型体としては発泡ポリスチレンからなる成型体が
あったが、脆いという致命的な欠点があるうえ、耐薬品
性に劣るという欠点があり、早くからその改善が望まれ
ていた。かがる欠点を解決するものとして架橋した発泡
ポリエチレンからなる成型体が提案された。しかしなが
らこの発泡ポリエチレン成型体は圧縮強度等構造材、建
材として要求される機械的強度が小さいという欠点があ
った。
Moldings made of foamed polystyrene have been used as foam moldings, but they have the fatal drawback of being brittle and have poor chemical resistance, and improvements to these problems have long been desired. A molded body made of crosslinked polyethylene foam was proposed as a solution to the drawback of sagging. However, this foamed polyethylene molded product has a drawback in that it has low mechanical strength such as compressive strength, which is required for structural and building materials.

夫屹 本発明は上記従来技術の欠点を解消した新葺なポリプロ
ピレン系合成樹脂発泡成型体を提供する特Kll械的強
度が審い発泡成型体を得るべく鋭意研究した結果、41
定の密度および気泡膜厚を有するポリプロピレン系合成
樹脂発泡成型体が良好な性質を有することを見出し1本
発明を完成するに至った。
The present invention provides a new polypropylene-based synthetic resin foam molded product that eliminates the drawbacks of the above-mentioned conventional technology.As a result of intensive research to obtain a foam molded product with high mechanical strength,
The present inventors have discovered that a polypropylene synthetic resin foam molded product having a certain density and cell thickness has good properties, and has completed the present invention.

すなわち本発明は、予備発泡粒子を、閉鎖し得るが密閉
し得ない型に充填し、加熱して前記粒子を発泡させて得
られる成型体において、該成型体はポリプロピレン系合
成樹脂発泡体からなr、s度0.06〜0.3g/d、
気泡膜厚1〜50μでおることを特徴とするポリプロピ
レン系合成樹脂発泡成型体を要旨とするものである。
That is, the present invention provides a molded article obtained by filling a mold that can be closed but not sealed with pre-expanded particles and foaming the particles by heating, the molded article being made of a polypropylene synthetic resin foam. r, s degree 0.06-0.3 g/d,
The gist is a polypropylene-based synthetic resin foam molded product characterized by a cell membrane thickness of 1 to 50 microns.

本発明のポリプロピレン系合成樹脂発泡成型体を得るに
当っては、高密度の予備発泡粒子が用いられ、この予備
発泡粒子の社質としては、エチレン−プロピレンランダ
ム共重合体、エチレン−プロピレンブロック共重合体、
プロピレン単独1合体等が挙げられ、これらは架橋して
いてもいなくてもよいが無架橋のものが特に有益である
。上記した重合体のうち、エチレン−プルピレン2ンダ
ム共重合体が好ましく、*にエチレン成分0.5〜10
重量嗟の共重合体が好ましい。
In obtaining the polypropylene synthetic resin foam molded product of the present invention, high-density pre-expanded particles are used, and the properties of the pre-expanded particles include ethylene-propylene random copolymer, ethylene-propylene block copolymer, etc. polymer,
Examples include propylene alone and monomer, and these may or may not be crosslinked, but non-crosslinked ones are particularly useful. Among the above-mentioned polymers, ethylene-propylene di-random copolymer is preferable, and * has an ethylene component of 0.5 to 10
Heavy weight copolymers are preferred.

本発明に用いられる高密度のポリプロピレン系合成樹脂
予備発泡粒子は例えば次のような予備発泡方法によって
製造することができる。すなわち。
The high-density polypropylene synthetic resin pre-expanded particles used in the present invention can be produced, for example, by the following pre-expanding method. Namely.

重合体粒子内に揮発性発泡剤を含有させる工程。A step of incorporating a volatile blowing agent into the polymer particles.

密閉容器内で重合体粒子を分散媒に分散させ所定温度に
加熱する工程、および容器の一端を開放し。
A step of dispersing the polymer particles in a dispersion medium and heating them to a predetermined temperature in a closed container, and opening one end of the container.

上記粒子と分散媒を同FrfK容器内よシも低圧の雰囲
気下に放出する工程よりなる予備発泡方法によって製造
することができる。
It can be produced by a pre-foaming method comprising a step of releasing the particles and dispersion medium into the same FrfK container under a low pressure atmosphere.

この方法に用いる揮発性発泡剤としては2例えばプロパ
ン、ブタン、ペンタン、ヘキサン、ヘプタン等で例示さ
れる脂肪族炭化水素類、シクロブタン、シクロペンタン
等で例示される環式脂肪族炭化水素類及びトリクロロク
ロロメタン、ジクロロシフpロメタン、ジクμロチドラ
フロロエタン。
Volatile blowing agents used in this method include aliphatic hydrocarbons such as propane, butane, pentane, hexane, heptane, etc., cycloaliphatic hydrocarbons such as cyclobutane, cyclopentane, etc., and trichloro Chloromethane, dichlorosifu-promethane, dichlorothidrafluoroethane.

メチルクロライド、エチルクロライド、メチレンクロラ
イド等で例示されるハロゲン化炭化水素類等が使用され
る。この発泡剤の添加量は通常重合体粒子100重量部
に対し5〜30重量部用いられる。
Halogenated hydrocarbons such as methyl chloride, ethyl chloride, methylene chloride, etc. are used. The amount of the blowing agent added is usually 5 to 30 parts by weight per 100 parts by weight of the polymer particles.

この方法では重合体粒子と揮発性発泡剤を別々KII1
.いは揮発性発泡剤を重合体粒子に含有させた後分散媒
に分散させるが、このとき要すれば分散剤2例えば微粒
状の酸化アルミニウムおよび酸化チタン、塩基性炭酸マ
グネシウム、塩基性炭酸亜鉛、炭酸カルシウム郷を用い
ることができる。この分散剤の添加量は通常重合体粒子
100重量部に対し0.01〜10重量部である。また
分散媒は重合体粒子を溶解させない溶媒であればよく2
例えば水、エチレングリコール、グリセリン、メタノー
ル、エタノール等のうちの1種又はそれらの2種以上の
混合物が例示されるが通常は水が好ましい。
In this method, the polymer particles and the volatile blowing agent are separated into KII1.
.. Alternatively, a volatile blowing agent is incorporated into the polymer particles and then dispersed in a dispersion medium. At this time, if necessary, a dispersant 2 such as finely divided aluminum oxide and titanium oxide, basic magnesium carbonate, basic zinc carbonate, Calcium carbonate can be used. The amount of this dispersant added is usually 0.01 to 10 parts by weight per 100 parts by weight of the polymer particles. The dispersion medium may be any solvent that does not dissolve the polymer particles.
Examples include water, ethylene glycol, glycerin, methanol, ethanol, etc., or a mixture of two or more thereof, but water is usually preferred.

この方法では容器の一端を開放して重合体粒子と分散媒
とを同時に容器内よ〕も低圧の雰囲気下に放出するが、
このときの容器内の圧力は揮発性発泡剤Os気圧以上ま
たは以下のいずれでもよく。
In this method, one end of the container is opened and the polymer particles and dispersion medium are simultaneously discharged into the container into a low-pressure atmosphere.
The pressure inside the container at this time may be either higher than or lower than the volatile blowing agent Os atmospheric pressure.

放出する雰囲気は通常常圧の雰囲気が選ばれる。The atmosphere to be released is usually an atmosphere of normal pressure.

このようKして得られる高v!i度の予備発泡粒子は1
発泡時0Il1度、圧力1発泡剤の量等によりても異な
るが2通常3〜20倍の見掛は発泡倍率を有する。
The high v obtained by doing K like this! i degree pre-expanded particles are 1
At the time of foaming, it has an apparent expansion ratio of 0Il1 degree, pressure 1, amount of blowing agent, etc., but usually 3 to 20 times.

次いで予備発泡粒子は常温、常圧下熟成後加圧熟成され
る。加圧熟成は通常無機ガスまたは無機ガスと揮発性発
泡剤との混合ガスによシ0.3〜8ky / m (G
)で3〜72時間行なわれ、これKよって予備発泡粒子
内に0.3〜5 kg/ cd (G)、好ましくは3
ky/d(G)以下の内圧が付与される。無機ガスとし
て祉、空気、窒素、アルゴン、−\リウム等が用いられ
る。
Next, the pre-expanded particles are aged at room temperature and pressure, and then aged under pressure. Pressure aging is usually carried out using an inorganic gas or a mixed gas of an inorganic gas and a volatile blowing agent at a rate of 0.3 to 8 ky/m (G
) for 3 to 72 hours, thereby adding 0.3 to 5 kg/cd (G), preferably 3
An internal pressure of ky/d (G) or less is applied. As the inorganic gas, air, nitrogen, argon, -\lium, etc. are used.

上記の如く内圧を付与された予備発泡粒子は。The pre-expanded particles are subjected to internal pressure as described above.

該粒子を閉鎖し得るが密閉し得ない金型・例えば型面に
水蒸気郷の加熱媒体が通過できる小孔を有する金型に充
填し1例えば2〜5 ky / cj (G)の水蒸気
を用いて加熱膨張させることによシ型通シの本発明のポ
リプロピレン系合成樹脂発泡成型体が得られる。
A mold that can close the particles but cannot be sealed, for example, a mold having small holes in the mold surface through which a heating medium of steam can pass, is filled with steam of 1 to 5 ky/cj (G), for example. By heating and expanding the polypropylene-based synthetic resin foam molded product of the present invention, a polypropylene-based synthetic resin foam molded product of the present invention is obtained.

上記のようKして得られる本発明のポリプロピレン系合
成樹脂発泡成型体は、密度が0.06〜0,3I/−2
気泡膜厚が1〜50μである。密度が0.06117d
未満では発泡成型体の機械的強度が小さ過ぎ1例えば構
造材、建材等に用いることができず。
The polypropylene synthetic resin foam molded product of the present invention obtained by K as described above has a density of 0.06 to 0.3 I/-2
The bubble film thickness is 1 to 50μ. Density is 0.06117d
If it is less than 1, the mechanical strength of the foamed molded product is too low to be used for, for example, structural materials, building materials, etc.

o、sl/dを超える場合・Kは発泡成型体の重量が増
加し1発泡体の利点である軽盪化が困難と彦るうえ2表
面保護性が充分でない。向、密度の好ましい範囲は0.
07〜0.1.p/cIlである。また気泡膜厚が1μ
未満で祉成型体は柔軟性が充分でなく(腰が弱くル曲げ
Kよる破断が起こ夛易く、50μを超える場合には表面
保護性が著しく損なわれ。
If K exceeds o, sl/d, the weight of the foamed molded product increases, 1. It is difficult to reduce the amount of abrasion, which is an advantage of foamed products, and 2. the surface protection property is not sufficient. The preferred range of direction and density is 0.
07-0.1. p/cIl. Also, the bubble film thickness is 1μ
If it is less than 50 μm, the molded product will not have sufficient flexibility (it is weak and will easily break due to bending), and if it exceeds 50 μm, the surface protection will be significantly impaired.

例えば包装材として用いる場合、j1品を傷っする虞れ
がある。
For example, when used as a packaging material, there is a risk of damaging the product.

本発明のポリプロピレン系合成樹脂発泡成型体は例えば
包装材、緩衝材、構造材、ms、車輛部材等圧用いるこ
とができ、特に機械的強度が要求される重量物の包装材
、カバンの芯材等の構造材。
The polypropylene synthetic resin foam molded product of the present invention can be used, for example, in packaging materials, cushioning materials, structural materials, MS, vehicle parts, etc. In particular, packaging materials for heavy items that require mechanical strength, and core materials for bags. Structural materials such as

断熱材等の建材、自動車のドア、天井、座席の芯材等の
車輌部材等に有効に用いることができる。
It can be effectively used for building materials such as heat insulating materials, and vehicle components such as core materials for automobile doors, ceilings, and seats.

以上説明したように、特定の密度および気泡膜厚を有す
る本発明のポリプロピレン系合成樹脂発泡成型体は圧縮
硬さ、柔軟性(腰の強さ)4!の機械的強度が大きく9
表面保護性も良好であり2例えば比較的大きい機械的強
度が要求される重量物の包装材、構造材、建材、車輌部
材等に用いる場合特に有益なものである。
As explained above, the polypropylene synthetic resin foam molded product of the present invention having a specific density and cell thickness has a compression hardness and flexibility (resilience) of 4! The mechanical strength of
It also has good surface protection properties and is particularly useful when used, for example, in packaging materials for heavy objects, structural materials, building materials, vehicle parts, etc., which require relatively high mechanical strength.

以下、実施例および比較例を掲げて本発明をさらに詳細
に説明する。
Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples.

実施例1〜3および比較例1〜5 エチレン−プロピレンランダムux合体粒子<:r−藁 チレン成分重量%)iooxi部、ジクロロジフロロメ
タン5〜50重量部、微粒状酸化アルミニウム0.3x
量部および水300重M部を密閉容器内に入れ、攪拌下
135〜150°(7に加熱して上記粒子にジクロロシ
フp−メタンを含有させた。
Examples 1 to 3 and Comparative Examples 1 to 5 Ethylene-propylene random ux combined particles <:r-straw tyrene component weight%) iooxi part, dichlorodifluoromethane 5 to 50 parts by weight, fine particulate aluminum oxide 0.3x
parts and 300 parts by weight of water were placed in a closed container and heated to 135-150° (7°C) while stirring to incorporate dichloroschif-p-methane into the particles.

次いで容器内の圧力k 20 ms o、ky/cj(
G) K保持しながら重合体粒子と水とを同時に大気下
へ放出し、乾燥させて予備発泡粒子を得だ。同、ジクロ
ロジフロロメタンの門は上記の範しムトで種々変えて行
なった。得られた予備発泡粒子を加圧容器内に入れ、 
 2kg/m(G)の空気にて100時間加圧熟成して
内圧を付与した稜、予備発泡粒子を金型に充填し、3.
5〜5 kg / c#1(G)の水蒸気により加熱し
て発泡膨張させ第1表に示す如き密度および気泡膜厚を
有する型通りの発泡成型体を得た。得られた発泡成楯体
の各々について圧縮波62表面保鰻性および柔軟性試験
を行なった。結果を第1表に示す。
Then, the pressure inside the container k 20 ms o, ky/cj (
G) While retaining K, polymer particles and water were simultaneously released into the atmosphere and dried to obtain pre-expanded particles. Similarly, dichlorodifluoromethane was tested using the above-mentioned method with various changes. The obtained pre-expanded particles are placed in a pressurized container,
Fill a mold with the ridge and pre-expanded particles that have been pressurized and aged in air at 2 kg/m (G) for 100 hours to give internal pressure; 3.
The foam was expanded by heating with water vapor at 5 to 5 kg/c#1 (G) to obtain a foam molded product having the density and cell thickness as shown in Table 1. Compression wave 62 surface integrity and flexibility tests were conducted on each of the foamed shields obtained. The results are shown in Table 1.

第1表 ※1−圧縮硬さの測定はJIS K6767に準じて行
なった。−;評価は9ゆ/cIi以上が◎、2ゆ/−以
上9ゆ/−未ン0.2ゆ/−未満が×を示す。
Table 1 *1 - Measurement of compression hardness was performed according to JIS K6767. -: Evaluation is ◎ if it is 9 yu/cIi or more, and × if it is 2 y/cIi or more and 9 y/cIi or less and less than 0.2 y/cIi.

※2−表面保饅性試験は硬質化粧板との摩擦により行な
りi※3−柔軟性試験はNDS z0503に準じて9
0”曲げて行iりた。
*2-Surface retention test is conducted by friction with hard decorative board.i*3-Flexibility test is 9 in accordance with NDS z0503.
0" bend.

Claims (1)

【特許請求の範囲】 予備発泡粒子を、閉鎖し得るが密閉し得ない型に充填し
、加熱して前記粒子を発泡させて得られる成型体におい
て、該成型体はポリプロピレン系合成樹脂発泡体からな
り、密度0.06〜0.3N/all。 気ft11[厚1〜50μであることを特徴とするポリ
プロピレン系合成樹脂発泡成型体。
[Scope of Claims] A molded article obtained by filling a mold that can be closed but not sealed with pre-expanded particles and foaming the particles by heating, the molded article being made of polypropylene synthetic resin foam. The density is 0.06 to 0.3 N/all. ft11 [A polypropylene-based synthetic resin foam molded product characterized by having a thickness of 1 to 50 μm.
JP56175991A 1981-11-02 1981-11-02 Polypropylene synthetic resin foamed and molded body Granted JPS5876228A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56175991A JPS5876228A (en) 1981-11-02 1981-11-02 Polypropylene synthetic resin foamed and molded body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56175991A JPS5876228A (en) 1981-11-02 1981-11-02 Polypropylene synthetic resin foamed and molded body

Publications (2)

Publication Number Publication Date
JPS5876228A true JPS5876228A (en) 1983-05-09
JPH0139335B2 JPH0139335B2 (en) 1989-08-21

Family

ID=16005785

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56175991A Granted JPS5876228A (en) 1981-11-02 1981-11-02 Polypropylene synthetic resin foamed and molded body

Country Status (1)

Country Link
JP (1) JPS5876228A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0963827A2 (en) * 1998-06-11 1999-12-15 Jsp Corporation Molded article of foamed and expanded beads of propylene resin

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5646735A (en) * 1979-09-25 1981-04-28 Japan Styrene Paper Co Ltd Freparation of polyolefin series resin foamed molding body

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5646735A (en) * 1979-09-25 1981-04-28 Japan Styrene Paper Co Ltd Freparation of polyolefin series resin foamed molding body

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0963827A2 (en) * 1998-06-11 1999-12-15 Jsp Corporation Molded article of foamed and expanded beads of propylene resin
EP0963827A3 (en) * 1998-06-11 2000-04-05 Jsp Corporation Molded article of foamed and expanded beads of propylene resin

Also Published As

Publication number Publication date
JPH0139335B2 (en) 1989-08-21

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