JPS58215327A - Manufacture of polyolefin resin molding foamed in force - Google Patents

Manufacture of polyolefin resin molding foamed in force

Info

Publication number
JPS58215327A
JPS58215327A JP57098836A JP9883682A JPS58215327A JP S58215327 A JPS58215327 A JP S58215327A JP 57098836 A JP57098836 A JP 57098836A JP 9883682 A JP9883682 A JP 9883682A JP S58215327 A JPS58215327 A JP S58215327A
Authority
JP
Japan
Prior art keywords
pressure
particles
polyolefin resin
force
internal pressure
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
JP57098836A
Other languages
Japanese (ja)
Inventor
Shohei Yoshimura
吉村 正平
Hideki Kuwabara
英樹 桑原
Toru Yamaguchi
徹 山口
Yoshimi Sudo
好美 須藤
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 JP57098836A priority Critical patent/JPS58215327A/en
Publication of JPS58215327A publication Critical patent/JPS58215327A/en
Pending 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
    • B29C44/3461Making or treating expandable particles
    • 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

Abstract

PURPOSE:To mass produce a foamed molding with limited use of energy employing a small equipment by heat foaming more than one kind of polyolefin resin prefoamed particles different in the internal pressure after it is mixed to fill a force. CONSTITUTION:100pts.wt. of ethylene-propylene random copolymer particles, 10- 20pts.wt. of dichlorodifluoromethane, 1pt.wt. of fine grannular aluminum oxide and 100pts.wt. of water are placed into an autoclave and heated under agitation. After it is heated to 140-150 deg.C, one end of the vessel is opened and the polymer and water are released under the atmosphere simultaneously to obtain prefoamed particles, a part of which is imparted an internal pressure by pressure curing. The prefoamed particles pressure cured and not fill a force at a specified mixing rate and undergoes a heat foaming with the steam of 2.6kg/cm<2>G to obtain a foamed molding.

Description

【発明の詳細な説明】 本発明はポリオレフィン樹脂屋内発泡成型体の製造法に
関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a polyolefin resin indoor foam molded product.

従来より合成樹脂発泡成形体2例えばポリスチレン発泡
成形体、ポリエチレン発泡成形体等が包装材、緩衝材等
多方面に用いられている。これらの発泡成形体は例えば
押出成形または予備発泡粒子を用いる所謂ビーズ成型法
にょシ製造されている。ここでビーズ成型法にょ)ポリ
オレフィン系樹脂発泡成型体を得る場合には予備発泡粒
子製造後、加圧熟成を行なって上記予備発泡粒子に所望
の内圧を付与し、しかる後この予備発泡粒子を成型用型
内に充填し加熱発泡して発泡成型体を得ていた。しかし
ながら、この方法では発泡成型体の生産量の増大に伴な
って加圧熟成用の加圧タンク等の設備も拡大する必要が
あり、また加圧熟成に使用されるエネルギーも増大する
という欠点がある。
Conventionally, synthetic resin foam moldings 2 such as polystyrene foam moldings and polyethylene foam moldings have been used in a wide variety of applications such as packaging materials and cushioning materials. These foam molded bodies are produced, for example, by extrusion molding or by the so-called bead molding method using pre-expanded particles. (bead molding method here) When obtaining a polyolefin resin foam molded product, after producing the pre-expanded particles, pressure aging is performed to impart a desired internal pressure to the pre-expanded particles, and then the pre-expanded particles are molded. It was filled into a mold and heated and foamed to obtain a foamed molded product. However, this method has the disadvantage that it is necessary to expand equipment such as pressure tanks for pressure aging as the production volume of foam moldings increases, and the energy used for pressure aging also increases. be.

本発明は上記従来技術の欠点を解消したポリオレフィン
樹脂屋内発泡成型体の製造法を提供することを目的とす
るものであって2本発明者らは上記目的を達成すべく鋭
意研究した結果、内圧が異なる2種以上の予備発泡粒子
を混合して用いることによシ加圧タンク等の設備を大型
化することなく大量に製造することができ、エネルギー
の使用量も少量で済み、かつ得られる発泡成型体は従来
品と同等またはそれ以上の成型性、物理的性質を有する
ことを見出すと共に七の製造方法の開発に成功し2本発
明を完成するに至った。
The purpose of the present invention is to provide a method for producing a polyolefin resin indoor foam molded product that eliminates the drawbacks of the above-mentioned prior art. By mixing and using two or more types of pre-expanded particles with different values, it is possible to produce in large quantities without increasing the size of equipment such as pressurized tanks, and the amount of energy used is small. They discovered that foam molded products have moldability and physical properties that are equal to or better than conventional products, and also succeeded in developing a manufacturing method (7), leading to the completion of the present invention (2).

すなわち2本発明は内圧が異なる2s以上のポリオレフ
ィン樹脂予備発泡粒子を成型用型内に混合充填した後加
熱発泡することを特徴とする特許オレフィン樹脂型内発
泡成型体の製造法を要旨とするものである。
In other words, the gist of the present invention is a patented method for producing an in-mold foamed olefin resin article, which is characterized in that pre-expanded polyolefin resin particles of 2 seconds or more with different internal pressures are mixed and filled into a mold and then heated and foamed. It is.

本発明において、ポリオレフィン樹脂予備発泡粒子の材
質としては2例えば低密度ポリエチレン(以下、LDP
Eと略称する。)、直鎖低密度ポリエチレン(以下、L
LDPEと略称する。)。
In the present invention, the material of the pre-expanded polyolefin resin particles is 2, for example, low density polyethylene (hereinafter referred to as LDP).
It is abbreviated as E. ), linear low-density polyethylene (hereinafter referred to as L
It is abbreviated as LDPE. ).

高密度ポリエチレン(以下、HDPEと略称する。)等
のポリエチレン、ポリプロピレン単独重合体。
Polyethylene and polypropylene homopolymers such as high-density polyethylene (hereinafter abbreviated as HDPE).

エチレンーグロビレン共重合体等のポリプロピレン系樹
脂、エチレン−α−オレフィン共X合体。
Polypropylene resins such as ethylene-globylene copolymers, ethylene-α-olefin co-X polymers.

プロピレン−α−オレフィン共重合体、 エチレン−ブ
タジェン共重合体、ポリブテン等が挙げられる。歯、上
記ポリオレフィン樹脂は架橋したもの無架橋の、ものい
ずれも用いることができるが無架橋のものが有益である
Examples include propylene-α-olefin copolymer, ethylene-butadiene copolymer, and polybutene. Both crosslinked and non-crosslinked polyolefin resins can be used, but non-crosslinked ones are advantageous.

本発明に用いられるポリオレフィン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1重合体粒子内に揮発性発泡剤を含有
させる工程、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
、上記粒子と分散媒を同時に容器内よシも低圧の雰囲気
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。
The pre-expanded polyolefin resin particles used in the present invention can be produced, for example, by the following pre-expanding method. That is, a step of incorporating a volatile blowing agent into one polymer particle, a step of dispersing the polymer particles in a dispersion medium in a closed container and heating it to a predetermined temperature, and a step of opening one end of the container and dispersing the particles and the dispersion medium. At the same time, the inside of the container can also be manufactured by a pre-foaming method comprising a step of releasing the foam into 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、およびトリクロ
ロフロロメタン、ジクロロシフ0ロメタン、ジクロロテ
トラフロロエタン、メチルクロライド、エチIレクロラ
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5〜40重量部重量部−ら
れる。
Volatile blowing agents used in this method include 2, for example, aliphatic hydrocarbons such as propane, butane, pentane, hexane, heptane, etc., cycloaliphatic hydrocarbons such as cyclobutane, cyclopentane, etc.; Halogenated hydrocarbons such as trichlorofluoromethane, dichlorofluoromethane, dichlorotetrafluoroethane, methyl chloride, ethyl chloride, methylene chloride, etc. are used. The amount of the blowing agent added is usually 5 to 40 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に或い
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、炭酸カルシウム等を用いるこ
とができる。この分散剤の添加量は通常重合体粒子10
0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IMi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 dispersed in a dispersion medium either separately or after the volatile blowing agent is contained in the polymer particles. Also, titanium oxide, basic magnesium carbonate, basic zinc carbonate, calcium carbonate, etc. can be used. The amount of this dispersant added is usually 10 polymer particles.
The amount is 0.01 to 10 parts by weight relative to 0 parts by weight. The dispersion medium may be any solvent that does not dissolve the polymer particles2.For example, water, ethylene glycol, glycerin, methanol, ethanol, etc., or a mixture of two or more thereof, may be used as the dispersion medium, but water is usually used. preferable.

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りも低圧の雰囲気に放出するが、こ
のときの容器内の温度は90〜170℃が好ましく、圧
力は揮発性発泡剤の蒸気圧以上または以下のいずれでも
よく、放出する雰囲気は通常常圧の雰囲気が選ばれる。
In this method, one end of the container is opened and the polymer particles and dispersion medium are simultaneously released into an atmosphere with a lower pressure than the inside of the container. At this time, the temperature inside the container is preferably 90 to 170°C, and the pressure is volatile. The pressure may be higher than or lower than the vapor pressure of the blowing agent, and the atmosphere to be discharged is normally selected to be at normal pressure.

このようにして得られる予備発泡粒子は揮発性発泡剤の
量、温度、圧力等によっても異なるが通常0.01〜0
.597 crlの密度を有する。
The pre-expanded particles obtained in this way vary depending on the amount of volatile blowing agent, temperature, pressure, etc., but are usually 0.01 to 0.
.. It has a density of 597 crl.

得られた予備発泡粒子は要すれば常温常圧下熟成され2
次いで要すれば予備発泡粒子を加圧タンク等に入れ、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
り加圧熟成して粒子内に内圧を付与する。無機ガスとし
ては9例えば空気。
The obtained pre-expanded particles are aged at room temperature and pressure if necessary.
Next, if necessary, the pre-expanded particles are placed in a pressurized tank or the like, and subjected to pressure ripening using an inorganic gas or a mixed gas of an inorganic gas and a volatile blowing agent to impart internal pressure within the particles. Examples of inorganic gases include air.

窒素、アルゴン、ヘリウム等が用いられる。Nitrogen, argon, helium, etc. are used.

本発明において、内圧が異なる2種以上の予備発泡粒子
を用いるが1通常は一方が加圧熟成によシ内圧を付与さ
れたもの、他方は加圧熟成を行なわない製造直後、また
は常温常圧下熟成したものを用いる。加圧熟成を行なっ
た予備発泡粒子の内圧は特に限定されないが0.5〜1
0klil/1(G)の範囲が好ましい。内圧が0.5
 kl?/cj (G)未満では加圧養生タンクの容積
を低減するという効果が発揮できない傾向があり、内圧
がxokg/1(G)t−超える場合には粒子内圧の保
持状態が不安定となり成形条件の許容範囲が極端に狭く
なる傾向がある。
In the present invention, two or more types of pre-expanded particles with different internal pressures are used; one is usually one that has been given internal pressure by pressure aging, and the other that is prepared immediately after production without pressure aging, or at room temperature and normal pressure. Use matured ones. The internal pressure of the pre-expanded particles subjected to pressure aging is not particularly limited, but is between 0.5 and 1.
A range of 0 klil/1 (G) is preferred. Internal pressure is 0.5
kl? /cj (G), there is a tendency that the effect of reducing the volume of the pressurized curing tank cannot be achieved, and if the internal pressure exceeds xokg/1 (G)t-, the maintenance state of the particle internal pressure becomes unstable and the molding conditions The tolerance range tends to be extremely narrow.

本発明において、予備発泡粒子の内圧は下記式によシ、
求めたものである。
In the present invention, the internal pressure of the pre-expanded particles is determined by the following formula:
It's what I asked for.

(式中、Wpは加圧熟成後の予備発泡粒子の重量、Wo
は常圧下充分熟成した予備発泡粒子の重量、0.082
は気体定数、tは測定時の温度、1.0332は気圧を
に9/−に換算する係数である。) 上記の予備発泡粒子を成型用型内に混合充填するに当っ
て、内圧が高いものAと低いものBとの混合比(容積)
A: Bは特に限定されないが1:10〜3:1の範囲
が好ましい。また予備発泡粒子の混合充填は内圧の同じ
のものが集合せず分散状態で行なうこと亡妻が好ましく
、また同じ材質のものを用いることが好ましい。同、内
圧が異なる予備発泡粒子を3種類以上混合してもよく、
加圧熟成したものを2種類混合してもよい。
(In the formula, Wp is the weight of the pre-expanded particles after pressure ripening, Wo
is the weight of pre-expanded particles sufficiently aged under normal pressure, 0.082
is a gas constant, t is the temperature at the time of measurement, and 1.0332 is a coefficient for converting the atmospheric pressure into 9/-. ) When mixing and filling the above pre-expanded particles into a mold, the mixing ratio (volume) of particles A with high internal pressure and particles B with low internal pressure.
A:B is not particularly limited, but is preferably in the range of 1:10 to 3:1. In addition, it is preferable that the pre-expanded particles be mixed and filled in a dispersed state so that particles with the same internal pressure do not aggregate, and it is preferable to use particles made of the same material. Similarly, three or more types of pre-expanded particles having different internal pressures may be mixed,
Two types of pressure-ripened products may be mixed.

本発明において、成型用型としてti2例えば型面に加
熱媒体が通過する多数の小孔を有する通常の成型用金型
を用いることができ、加熱媒体として例えば11〜4.
0 kg / at (G)の水蒸気を用いて予備発泡
−粒子を加熱発泡して型通シの発泡成型体を得ることが
できる。
In the present invention, as the molding mold, for example, a normal molding mold having a large number of small holes on the mold surface through which a heating medium passes can be used.
The pre-foamed particles are heated and foamed using water vapor of 0 kg/at (G) to obtain a molded foamed product.

本発明により得られるポリオレフィン樹脂型内発泡成型
体は例えば包装材、緩衝材、保温材、断熱材、N築資材
、車輛部材、浮揚材2食品容器等に用いることができる
The polyolefin resin in-mold foam molded product obtained by the present invention can be used for, for example, packaging materials, cushioning materials, heat insulating materials, heat insulating materials, N construction materials, vehicle parts, flotation material 2 food containers, and the like.

以上説明したように1本発明によれば、内圧が異なる2
種以上のポリオレフィン樹脂予備発泡粒子を用いて型内
発泡成製体を得るので予備発泡粒子をすべて加圧熟成す
る必要がないため加圧タンク等の設備を拡大することな
く生産量を増大することができ、また必要な手間、エネ
ルギー等も少なくて済む等の利点を有するものであり、
また本発明によシ得られる発泡成型体は従来品と同等ま
たはそれ以上の成型性、外観、物理的性質を有するもの
である。
As explained above, 1. According to the present invention, 2.
Since an in-mold foamed product is obtained using pre-expanded particles of polyolefin resin of more than 100%, there is no need to pressurize and ripen all the pre-expanded particles, so production can be increased without expanding equipment such as pressurized tanks. It has the advantage of being able to do this, and requires less effort, energy, etc.
Furthermore, the foamed molded product obtained by the present invention has moldability, appearance, and physical properties that are equivalent to or better than those of conventional products.

以下、実施例を掲け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.

実施例1〜4 エチレン成分2.5%のエチレンープロピレンランダム
共重合体粒子100重量部、ジクロロシフa 四メp 
710〜20重量部、微粒状酸化アルミニウム1重量部
、水300重量部をオートクレーブに入れ、攪拌上加熱
して140〜150’Cに昇温した後容器の一端を開放
して重合体粒子と水と全同時に大気下に放出して密度0
.03〜o、osg/cdの予備発泡粒子を得た。
Examples 1 to 4 100 parts by weight of ethylene-propylene random copolymer particles containing 2.5% ethylene component, dichlorosif a, four mep
Put 710 to 20 parts by weight, 1 part by weight of finely divided aluminum oxide, and 300 parts by weight of water into an autoclave, stir and heat to raise the temperature to 140 to 150'C, then open one end of the container to separate the polymer particles and water. It is released into the atmosphere at the same time and the density becomes 0.
.. Pre-expanded particles of 03-0, osg/cd were obtained.

得られた予備発泡粒子を常温、常圧にて48時間熟成し
た後その一部を加圧タンクに入れ、空気によシ加圧熟成
して第1表に示す内圧を付与した。
The obtained pre-expanded particles were aged for 48 hours at normal temperature and pressure, and then a portion thereof was placed in a pressurized tank and aged under pressure with air to give the internal pressure shown in Table 1.

次いで加圧熟成を行なった予備発泡粒子と行なわなかっ
たものを第1表に示す混合比で長さ3001×幅3oo
cmx厚さ30cmの成型用金型内に混合充填し、  
2.6 ’q/cd (G)の蒸気で加熱発泡させて発
泡成型体を得た。得られた発泡成型体の成型性および外
観は良好であ)、また加圧タンクの使用量は従来の方法
に鴨べて1/2〜1/3必要としただけであった。
Next, the pre-expanded particles that were subjected to pressure aging and those that were not subjected to pressure aging were mixed at the mixing ratio shown in Table 1, and were made into 3001 mm long x 30 mm wide particles.
Mixed and filled into a mold of cm x 30 cm thick,
A foamed molded product was obtained by heating and foaming with 2.6'q/cd (G) steam. The moldability and appearance of the resulting foamed product were good), and the amount of pressurized tanks required was only 1/2 to 1/3 compared to the conventional method.

実施例5,6 エチレン−プロピレンランダム共重合体に代えてMI=
2.1 、mp =122℃、 d = 0.930 
l / adのLLDPEを用いた以外は実施例1と同
様に行なって予備発泡粒子を得た。得られた予備発泡粒
子の一部を加圧タンクに入れ、空気にて加圧熟成して第
1表に示す内圧を付与した。
Examples 5 and 6 MI=instead of ethylene-propylene random copolymer
2.1, mp = 122°C, d = 0.930
Pre-expanded particles were obtained in the same manner as in Example 1 except that LLDPE of l/ad was used. A part of the obtained pre-expanded particles was placed in a pressurized tank and aged under pressure with air to give the internal pressure shown in Table 1.

加圧熟成を行なった予備発泡粒子および加圧熟成を行な
わない予備発泡粒子を第1表に示す混合比で実施例1と
同様の成型用金型内に混合充填し。
Pre-expanded particles subjected to pressure ripening and pre-expanded particles not subjected to pressure ripening were mixed and filled into the same molding mold as in Example 1 at the mixing ratio shown in Table 1.

1、5 kg / c!IL(G)の蒸気で加熱発泡し
て良好な発泡成型体を得た。得られた発泡成型体の成型
性および外観は良好であり、tた加圧タンクの使用量は
従来の方法に較べて1/2〜1/3必要としただけであ
った0
1.5 kg/c! A good foam molded product was obtained by heating and foaming with the steam of IL(G). The moldability and appearance of the obtained foamed product were good, and the amount of pressurized tank required was only 1/2 to 1/3 compared to the conventional method.

Claims (1)

【特許請求の範囲】[Claims] 内圧が異なる2種以上のポリオレフィン樹脂予備発泡粒
子を成型用型内に混合充填した後加熱発泡することを特
徴とするポリオレフィン樹脂型内発泡成型体の製造法。
A method for producing an in-mold foamed polyolefin resin article, which comprises mixing and filling two or more pre-expanded polyolefin resin particles having different internal pressures into a mold and then heating and foaming them.
JP57098836A 1982-06-09 1982-06-09 Manufacture of polyolefin resin molding foamed in force Pending JPS58215327A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57098836A JPS58215327A (en) 1982-06-09 1982-06-09 Manufacture of polyolefin resin molding foamed in force

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57098836A JPS58215327A (en) 1982-06-09 1982-06-09 Manufacture of polyolefin resin molding foamed in force

Publications (1)

Publication Number Publication Date
JPS58215327A true JPS58215327A (en) 1983-12-14

Family

ID=14230350

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57098836A Pending JPS58215327A (en) 1982-06-09 1982-06-09 Manufacture of polyolefin resin molding foamed in force

Country Status (1)

Country Link
JP (1) JPS58215327A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5252270A (en) * 1990-12-20 1993-10-12 Basf Aktiengesellschaft Method of forming foam moldings having varied density regions
WO2006100517A1 (en) * 2005-03-24 2006-09-28 Zotefoams Plc Process for introducing a gas into a polymer

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4985158A (en) * 1972-12-19 1974-08-15

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4985158A (en) * 1972-12-19 1974-08-15

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5252270A (en) * 1990-12-20 1993-10-12 Basf Aktiengesellschaft Method of forming foam moldings having varied density regions
WO2006100517A1 (en) * 2005-03-24 2006-09-28 Zotefoams Plc Process for introducing a gas into a polymer
GB2439697A (en) * 2005-03-24 2008-01-02 Zotefoams Plc Process for introducing a gas into a polymer
GB2439697B (en) * 2005-03-24 2009-11-04 Zotefoams Plc Process for introducing a gas into a polymer
US8871823B2 (en) * 2005-03-24 2014-10-28 Zotefoams, PLC Process for introducing a gas into a polymer

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