JPS59172532A - Pre-expansion of polyolefin resin particle - Google Patents

Pre-expansion of polyolefin resin particle

Info

Publication number
JPS59172532A
JPS59172532A JP58047683A JP4768383A JPS59172532A JP S59172532 A JPS59172532 A JP S59172532A JP 58047683 A JP58047683 A JP 58047683A JP 4768383 A JP4768383 A JP 4768383A JP S59172532 A JPS59172532 A JP S59172532A
Authority
JP
Japan
Prior art keywords
polyolefin resin
resin particles
stirring
foaming
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.)
Granted
Application number
JP58047683A
Other languages
Japanese (ja)
Other versions
JPH0446976B2 (en
Inventor
Kyoichi Nakamura
中村 京一
Masao Ando
正夫 安藤
Kenichi Senda
健一 千田
Tatsuhiko Nishida
西田 建彦
Tadayuki Ichimura
忠行 市村
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.)
Kanegafuchi Chemical Industry Co Ltd
Original Assignee
Kanegafuchi Chemical Industry Co Ltd
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 Kanegafuchi Chemical Industry Co Ltd filed Critical Kanegafuchi Chemical Industry Co Ltd
Priority to JP58047683A priority Critical patent/JPS59172532A/en
Publication of JPS59172532A publication Critical patent/JPS59172532A/en
Publication of JPH0446976B2 publication Critical patent/JPH0446976B2/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
    • B29C44/3461Making or treating expandable particles

Abstract

PURPOSE:To obtain uniform pre-expanded particles, by dispersing polyolefin resin particles containing a volatile blowing agent in water with the aid of a dispersant and a surfactant in a pressure vessel equipped with a special H- shaped paddle, applying heat and pressure to the mixture and releasing the pressure. CONSTITUTION:An H-shaped paddle is secured to an agitator shaft so that it may slant toward the direction of agitation at an angle of 5-45 deg. with the vertical plane for the paddle. The special H-shaped paddle thus obtained is attached to a pressure vessel 1. In this vessel 1, polyolefin resin particles (e.g., polyethylene or polypropylene particles) containing a volatile blowing agent (e.g., propane) is dispersed in water with the aid of a dispersant (e.g., calcium tertiary phosphate) and a surfactant (e.g., sodium dodecylbenzenesulfonate). This dispersion is heated to the softening temperature of the resin particles or above and pressurized to the vapor pressure of the blowing agent or above and then discharged into a low-pressure zone to pre-expand the resin particles.

Description

【発明の詳細な説明】 本発明は、水中に分散せしめた高温高圧下の揮発性発泡
剤を含有するポリオレフィン系樹脂粒子を圧力開放する
ことにより予備発泡させる方法において、分散状態を極
めて安定ならしめる攪拌方法に関するものである。
Detailed Description of the Invention The present invention is a method for pre-foaming polyolefin resin particles containing a volatile blowing agent dispersed in water under high temperature and high pressure by releasing the pressure, which makes the dispersion state extremely stable. This relates to a stirring method.

従来、ポリオレフィン系樹脂粒子と揮発性発泡剤をオー
トクレーブなどの耐圧容器中にて水に分散させ、これを
高温高圧の状態にもたらした後、低圧域に放出すること
によりポリオレフィン系樹脂を予備発泡する方法は公知
であり、例えば西独公開特許公報第21076133号
、特公昭56−1344号等に記載されている。
Conventionally, polyolefin resin particles and a volatile foaming agent are dispersed in water in a pressure-resistant container such as an autoclave, brought to a high temperature and high pressure state, and then released into a low pressure area to pre-foam the polyolefin resin. The method is well known and is described, for example, in West German Published Patent Application No. 21076133, Japanese Patent Publication No. 56-1344, and the like.

上記方法においてはポリオレフィン系樹脂粒子と揮発性
発泡剤を撹拌によって水に分散させることの記載はある
が、H型攪拌翼、プロペラ、及びブルーマージンなどを
用いた普通の撹拌方法では、昇温後、低圧域に放出する
以前に耐圧容器中でポリオレフィン系樹脂粒子同志が互
いに凝集融着することがみられ、分散性が劣っていた。
In the above method, there is a description of dispersing polyolefin resin particles and a volatile blowing agent in water by stirring, but ordinary stirring methods using H-type stirring blades, propellers, blue margins, etc. However, it was observed that the polyolefin resin particles coagulated and fused together in the pressure container before being discharged into a low pressure region, resulting in poor dispersibility.

この理由としては、ポリオレフィン系樹脂粒子は一般的
に密度が1 ’f / cAより小さいものが多く、水
中で浮きやすいため通常の攪拌によっては、耐圧容器の
水中全体にわたってポリオレフィン系樹脂粒子を均一に
分散させることが困難であることが考えられる。これを
検討するため、H型攪拌翼を用いた実験で攪拌速度を種
々変更したところ、攪拌速度を速めればポリオレフィン
系樹脂粒子同志の凝集融着は少しは改善されるが完全に
は解決できなかった。又、別の方法として、加熱された
ポリオレフイノ系樹脂粒子が互いに融着することを防ぐ
ため、分散剤として炭酸カルシウム、*基性炭酸亜鉛、
塩基性炭酸マグネシウム、ピロリン酸カルシウム、第3
リン酸カルシウム等の無機化合物微粉末を添加すること
が知られている。しかし、これらを添加しても使用量が
少いと融着防止効果は少なく、完全な融着防止を行うに
は多量の分散剤を用いなけれはならなかった。しかも、
こうして得られた予備発泡粒子は、その後、金型に充填
し、蒸気等で加熱して型通りの発泡成形体とするが、該
予備発泡粒子の表面に分散剤が多量刊着しているため、
発泡粒子同志の融着性に劣り商品価値を減するという問
題があった。そこで本発明者らは、上記の従来技術の問
題点を解決すべく鋭意研究を行った結果、本発明に到達
した。
The reason for this is that polyolefin resin particles generally have a density smaller than 1'f/cA and tend to float in water, so normal stirring cannot uniformly spread the polyolefin resin particles throughout the water in the pressure container. It may be difficult to disperse. To investigate this, we conducted an experiment using an H-type stirring blade and varied the stirring speed, and found that increasing the stirring speed slightly improved the agglomeration and fusion of polyolefin resin particles, but it did not completely solve the problem. There wasn't. Alternatively, in order to prevent the heated polyolefin resin particles from fusing together, calcium carbonate, *basic zinc carbonate,
Basic magnesium carbonate, calcium pyrophosphate, tertiary
It is known to add fine powder of an inorganic compound such as calcium phosphate. However, even if these are added, if the amount used is small, the effect of preventing fusion is small, and in order to completely prevent fusion, it is necessary to use a large amount of dispersant. Moreover,
The pre-expanded particles obtained in this way are then filled into a mold and heated with steam etc. to form a foam molded product according to the mold, but since a large amount of dispersant is deposited on the surface of the pre-expanded particles. ,
There was a problem in that the adhesiveness of the expanded particles to each other was poor, reducing the commercial value. Therefore, the present inventors conducted intensive research to solve the problems of the above-mentioned prior art, and as a result, they arrived at the present invention.

即ち本発明は、耐圧容器内で、揮発性発泡剤を含有する
ポリオレフィン系樹脂粒子を水に分散させ、該粒子の軟
化温度以上の温度に加熱し、該発泡剤の蒸気圧以上の加
圧下で、該粒子と水との混合物を低圧域に放出するポリ
オレフィン系樹脂粒子の予備発泡方法におい石、該粒子
の水への分散は、分散剤と界面活性剤を使用し、H型攪
拌翼を該撹拌翼の垂面、面から撹拌方向側に傾斜させた
特殊H型攪拌翼で攪拌することを特徴とするポリオレフ
ィン系樹脂粒子の予備発泡方法を要旨とする。
That is, in the present invention, polyolefin resin particles containing a volatile blowing agent are dispersed in water in a pressure-resistant container, heated to a temperature higher than the softening temperature of the particles, and under a pressure higher than the vapor pressure of the blowing agent. , a pre-foaming method for polyolefin resin particles in which a mixture of the particles and water is discharged into a low-pressure region.Dispersion of the particles in water uses a dispersant and a surfactant, and an H-type stirring blade is used to disperse the particles in water. The gist of this invention is a method for pre-foaming polyolefin resin particles, which is characterized by stirring with a special H-shaped stirring blade that is inclined from the vertical surface of the stirring blade in the direction of stirring.

本発明の方法によれば、少量の分散剤を使用するだけで
耐圧容器内でのポリオレフィン系樹脂粒子同志の融着の
全くない均質な予備発泡粒子を得ることができる。
According to the method of the present invention, homogeneous pre-expanded particles without any fusion of polyolefin resin particles in a pressure container can be obtained by using only a small amount of dispersant.

本発明に用いるポリオレフィン系樹脂としては、低密度
ポリエチレン、中密度ポリエチレン、高密度ポリエチレ
ン、直鎖状低密度ポリエチレン、ポリプロピレン、エチ
レンープロピレンランダムコホIJマー、エチレン−プ
ロピレンブロックコポリマー、エチレン−酢酸ビニルコ
ポリマーなどが好ましく、エチレン−エチルアクリレー
トコポリマー、ポリブテン−1,エチレン−アクリル酸
金属塩型コポリマー(アイオノマー)、ポリ−4−メチ
ルペンテン−1等も使用できる。これらの樹脂の単独ま
たは2種以上のブレンド物、またはこれらの樹脂と充填
剤との混合物が使用できる。更に上記ポリオレフィン系
樹脂を有機過酸化物や放射線等により架橋させたものも
使用できる。
The polyolefin resin used in the present invention includes low density polyethylene, medium density polyethylene, high density polyethylene, linear low density polyethylene, polypropylene, ethylene-propylene random copolymer, ethylene-propylene block copolymer, ethylene-vinyl acetate copolymer. etc. are preferred, and ethylene-ethyl acrylate copolymer, polybutene-1, ethylene-acrylic acid metal salt type copolymer (ionomer), poly-4-methylpentene-1, etc. can also be used. These resins can be used alone or in a blend of two or more, or a mixture of these resins and a filler. Furthermore, those obtained by crosslinking the above-mentioned polyolefin resins with organic peroxides, radiation, etc. can also be used.

本発明におけるポリオレフィン系樹脂粒子の粒子径は、
砦に制限はないか、通常、粒子径が0.25〜10.0
7Imノもの、更に好ましくは0.5〜6、Q mrr
tのものか型内発泡成形用として好適に使用される。
The particle diameter of the polyolefin resin particles in the present invention is
There is no limit to the fort, usually the particle size is 0.25-10.0
7 Im, more preferably 0.5 to 6, Q mrr
It is suitable for use in in-mold foam molding.

本発明で使用される揮発性発泡剤としては、沸点が一5
0〜120°Cの炭化水素またはハロゲン化炭化水素、
例えばプロパン、ブタン、ペンタン・ヘキサン、ヘプタ
ン、シクロペンクン、シクロヘキサン、モノクロルメタ
ン、ジクロルメタン、モノクロルエタン、トリクロルモ
ノフルオルメタン。
The volatile blowing agent used in the present invention has a boiling point of
0-120°C hydrocarbon or halogenated hydrocarbon,
For example, propane, butane, pentane/hexane, heptane, cyclopenkune, cyclohexane, monochloromethane, dichloromethane, monochloroethane, trichloromonofluoromethane.

ジクロルジフルオルメタン、ジクロルモノフルオルメタ
ン、トリクロルトリフルオルエタン、ジクロルテトラフ
ルオルエタン等があげられる。これらは単独にあるいは
2種以上混合して使用してもよい。
Examples include dichlorodifluoromethane, dichloromonofluoromethane, trichlorotrifluoroethane, dichlorotetrafluoroethane, and the like. These may be used alone or in combination of two or more.

本発明においてポリでレフイン系樹脂粒子を水に分散さ
せるには、攪拌機付きの耐圧容器中に少量の分散剤を使
用して行なう。
In the present invention, polyrefin resin particles are dispersed in water using a small amount of dispersant in a pressure-resistant container equipped with a stirrer.

撹拌機は図面によって説明する。第1図の1は耐圧容器
、2は攪拌装置、3はH型撹拌叡を該撹拌翼の垂直面か
ら攪拌方向側に傾斜させた特殊H型攪拌翼である。第2
図は、通常のI−I全撹拌翼、第3図は本発明の特殊H
型攪拌翼を拡大して示したものである。本発明゛の特殊
H型攪拌翼の幅、肉厚、攪拌翼の枚数は特に制限するも
のではないが、幅は耐圧容器の内径の10%程度、肉厚
は撹拌時の負荷に対して強度が充分あるもの、攪拌翼の
枚数は通常2枚であれば充分である。材質は強度面で耐
えうるものなら特に制限はないが、腐食性等の面からス
テンレス製が好ましい。本発明の特殊H型攪拌子の垂直
面からの傾斜角度は5°乃至45゜の範囲で選択するこ
とができる。角度が5°未満では通常のH型攪拌翼とほ
とんど同じであり、また45°を越えると攪拌力が失わ
れるため、いずれも本発明の分散安定化効果が得られな
い。好ましい角度範囲は5°乃至30°、更に好ましい
角度範囲は5°〜20°である。
The stirrer will be explained with reference to the drawings. In FIG. 1, 1 is a pressure-resistant container, 2 is a stirring device, and 3 is a special H-type stirring blade in which the H-type stirring blade is inclined from the vertical surface of the stirring blade toward the stirring direction. Second
The figure shows the normal I-I full stirring blade, and Figure 3 shows the special H of the present invention.
This is an enlarged view of the type stirring blade. The width, wall thickness, and number of stirring blades of the special H-type stirring blade of the present invention are not particularly limited, but the width is approximately 10% of the inner diameter of the pressure vessel, and the wall thickness is determined to be strong enough to withstand the load during stirring. It is usually sufficient if the number of stirring blades is two. There are no particular restrictions on the material as long as it is durable, but stainless steel is preferred from the viewpoint of corrosion resistance. The angle of inclination of the special H-shaped stirrer of the present invention from the vertical plane can be selected within the range of 5° to 45°. If the angle is less than 5°, it is almost the same as a normal H-type stirring blade, and if it exceeds 45°, the stirring power is lost, so that the dispersion stabilizing effect of the present invention cannot be obtained in either case. A preferred angular range is 5° to 30°, and a more preferred angular range is 5° to 20°.

本発明の特殊H型攪拌翼を用いるとポリオレフィン系樹
脂粒子が極めて均一に分散して、粒子同志の凝集融着が
全く起こらなくなる理由としては、水中に分散させたポ
リオレフィン系樹脂粒子は密度かl f / cAより
低く、水面上に浮き上ろうとするが、H型攪拌翼に攪拌
方向側に傾斜させであるため、耐圧容器において水とポ
リオレフィン系粒子を容器の底部に運ぼうとする力が働
らくので、粒子の浮力を抑制して水中での粒子を耐圧容
器内で偏在させることなく極めて均一に分散させている
ためと考えられる。
The reason why the polyolefin resin particles are dispersed extremely uniformly when the special H-type stirring blade of the present invention is used, and no agglomeration and fusion of the particles occurs is that the polyolefin resin particles dispersed in water have a density of f/cA, the polyolefin particles tend to float on the water surface, but because the H-shaped stirring blades are tilted toward the stirring direction, a force that tries to transport the water and polyolefin particles to the bottom of the pressure container acts. This is thought to be due to the fact that the buoyancy of the particles is suppressed and the particles in the water are dispersed extremely uniformly within the pressure container without being unevenly distributed.

本発明において使用する分散剤としては、塩基性炭酸マ
グネシウム、塩基性炭酸亜鉛、ピロリン酸カルシウム、
第3リン酸カルシウム、炭酸カルシウム等がある。また
場合によっては、これらの無機物質と少量の界面活性剤
、例えばドデシルベンゼンスルホン酸ソーダ、α−オレ
フィンスルホン酸ソーダ、n−パラフィンスルホン酸ソ
ーダ等のアニオン界面活性剤を併用することもある。分
散剤の使用量は、ポリオレフイン系樹脂1oo重量部に
対して0.05〜1.0重量部、好ましくは0.1〜0
.7を縦部である。また界面活性剤の使用量は、ポリオ
レフィン系樹脂100重量部に対して0.001〜0.
1重量部、好ましくは0.001〜0.05重量部であ
る。本発明に好適な分散剤と界面活性剤は、第3リン酸
カルシウムとドデシルベンゼンスルホン酸ソーダ、又は
第3リン酸カルシウムとn−パラフィンスルホン酸ソー
ダである。
Dispersants used in the present invention include basic magnesium carbonate, basic zinc carbonate, calcium pyrophosphate,
Examples include tertiary calcium phosphate and calcium carbonate. In some cases, these inorganic substances may be used in combination with a small amount of a surfactant, such as an anionic surfactant such as sodium dodecylbenzenesulfonate, sodium α-olefinsulfonate, and sodium n-paraffinsulfonate. The amount of the dispersant used is 0.05 to 1.0 parts by weight, preferably 0.1 to 0 parts by weight, per 10 parts by weight of the polyolefin resin.
.. 7 is the vertical part. The amount of surfactant to be used is 0.001 to 0.00 parts by weight per 100 parts by weight of the polyolefin resin.
1 part by weight, preferably 0.001 to 0.05 part by weight. Dispersants and surfactants suitable for the present invention are tertiary calcium phosphate and sodium dodecylbenzenesulfonate, or tertiary calcium phosphate and sodium n-paraffinsulfonate.

本発明における加熱温度は、発泡剤を含んだ状態でのポ
リオレフィン系樹脂の軟化温度以上で、通常、該軟化温
度乃至該軟化温度+50°Cの範囲である。該軟化温度
は樹脂の種類及び発泡剤の種類及び量などによって上記
範囲内で適切に調整される。例えば、低密度ポリエチレ
ンとジクロルジフルオロメタンの組合せでは90〜14
0°C1エチレン−プロピレンランダムコポリマーとジ
クロルジフルオロメタンの組合せでは110〜160°
Cの範囲で発泡が可能であり、発泡剤の使用量と加熱温
度の設定により所望の発泡倍率の予備発泡粒子を得るこ
とができる。加熱温度が発泡剤を含んだ状態での該ポリ
オレフィン系樹脂の軟化温度以下では発泡が困難であり
、該軟化温度+50°Cを越えると樹脂の溶融粘度が低
くなりすぎるため、本発明の特殊1−(型攪拌翼をもっ
てしても耐圧容器内での粒子同志の融着を防止すること
はできない。
The heating temperature in the present invention is higher than the softening temperature of the polyolefin resin in a state containing a blowing agent, and is usually in the range of the softening temperature to the softening temperature +50°C. The softening temperature is appropriately adjusted within the above range depending on the type of resin and the type and amount of the blowing agent. For example, in the combination of low density polyethylene and dichlorodifluoromethane, 90 to 14
110-160° for the combination of 0°C1 ethylene-propylene random copolymer and dichlorodifluoromethane
Foaming is possible within the range of C, and pre-expanded particles with a desired expansion ratio can be obtained by adjusting the amount of blowing agent used and the heating temperature. If the heating temperature is below the softening temperature of the polyolefin resin containing a blowing agent, it is difficult to foam, and if the heating temperature exceeds the softening temperature +50°C, the melt viscosity of the resin becomes too low. - (Even with type stirring blades, it is not possible to prevent particles from fusing together in a pressure-resistant container.

本発明の方法において、低圧域に水と粒子を放出すると
きの耐圧容器内の圧力は、使用する揮発性発泡剤の蒸気
圧以上に保毎される。ここでいう揮発性発泡剤の蒸気圧
とは、ポリオレフィン系樹脂粒子に元旭剤を加熱、加圧
条件下で含浸させた系での蒸気圧であり、放出時に耐圧
容器内の圧力を揮発性発泡剤の蒸気圧以上に保持するた
めには、揮発性発泡剤(液体又は気体状)及び/又はN
2などの不活性ガスを導入して加圧すればよい。
In the method of the present invention, the pressure within the pressure vessel when water and particles are discharged into the low pressure region is maintained at a level higher than the vapor pressure of the volatile blowing agent used. The vapor pressure of the volatile blowing agent referred to here is the vapor pressure in a system in which polyolefin resin particles are impregnated with Genasahi agent under heated and pressurized conditions. To maintain the vapor pressure above the blowing agent, volatile blowing agent (liquid or gaseous) and/or N
What is necessary is to introduce an inert gas such as No. 2 and pressurize it.

ポリオレフィン系樹脂粒子の放出は、耐圧容器の開閉で
きる適当な開口をもった底部の一端から低圧域、通常は
大気圧下に放出する。
The polyolefin resin particles are discharged into a low pressure region, usually atmospheric pressure, from one end of the bottom of the pressure container that has a suitable opening that can be opened and closed.

このようにして粒子相互の融着が全くみられない、しか
も均一微細セルを有する発泡倍率5〜90倍の独立気泡
の予備発泡粒子が得られる。こうして得られた予(if
ff発泡粒子は養生、熟成後、更に加圧熟成を行って閉
鎖しうるが密閉し得ない金型に充填し、水蒸気等の加熱
方法により粒子相互を融着させ、所望の型形状の発泡成
形体となしうる。
In this way, closed-cell pre-expanded particles having an expansion ratio of 5 to 90 times and having uniform fine cells in which there is no fusion between the particles are obtained. The result obtained in this way is if
ff After curing and ripening, the foamed particles are further pressure-ripened and filled into a mold that can be closed but cannot be sealed, and the particles are fused together using a heating method such as steam, and foam molded into the desired mold shape. It can be used as a body.

以上の如く、本発明のポリオレフィン系樹脂予備発泡粒
子の製造方法によれば、特殊H型攪拌翼の使用によって
予備発泡前後に粒子同志の融着のない予備発泡粒子を得
ることができ、しかも無機系分散剤の使用量も極めて少
なくてすむため、該予備発泡粒子を使用して得られる成
形体は粒子間の融着が極めて優れており、蒸気使用量も
少なくなるという利点がある。
As described above, according to the method for producing pre-expanded polyolefin resin particles of the present invention, it is possible to obtain pre-expanded particles without fusion of particles before and after pre-foaming by using a special H-type stirring blade, and in addition, inorganic Since the amount of system dispersant used is extremely small, the molded article obtained using the pre-expanded particles has the advantage that the fusion between the particles is extremely excellent and the amount of steam used is also small.

以下、実施例及び比較例によって本発明を更に詳しく説
明する。部とあるのは全て重量部である。
Hereinafter, the present invention will be explained in more detail with reference to Examples and Comparative Examples. All parts are by weight.

実施例1 傾斜角度が10°の特殊H型攪拌翼が取付けられた、下
方に開放用バルブを有する内容積3.51のオートクレ
ーブに純水800部とエチレン−プロピレンランダム共
重合体粒子(エチレン含有量4.5重量%、粒径約2問
、Ml  9)100部、及び分散剤として第3リン酸
カルシウム(太平化学社製2粒径0.5〜2μ)0.5
部、ドデシルベンゼンスルホン酸ソーダ(花王石けん側
製ネオペレックスNo、25 ) 0.025部を入れ
、i’+:j拌しながらジクロルジフルオロメタン55
部を力1えた後、加熱して136°Cに昇温した。次い
で、分散の安定性をi’F価するため、この温度で3時
間放置した後オートクレーブの内圧を窒素で30 /c
g / c2!に保ちなからオートクレーブ下方のバ、
ルブを開放し、樹脂粒子と水の混合物を大気圧下に放出
して予備発泡を行った。得られた予備発泡粒子は粒子同
志の融着が全く認められないものであり、実質的に均一
微細な独立気泡からなり、発泡倍率40倍のものであっ
た。
Example 1 800 parts of pure water and ethylene-propylene random copolymer particles (ethylene-containing Amount: 4.5% by weight, particle size: about 2 questions, Ml: 9) 100 parts, and tertiary calcium phosphate (manufactured by Taihei Kagaku Co., Ltd., 2 particle size: 0.5-2μ) as a dispersant: 0.5
Add 0.025 parts of sodium dodecylbenzenesulfonate (Neoperex No. 25 manufactured by Kao Soap) and add 55 parts of dichlorodifluoromethane while stirring i'+:j.
After straining, the mixture was heated to 136°C. Next, in order to evaluate the stability of the dispersion, the internal pressure of the autoclave was reduced to 30/c with nitrogen after being left at this temperature for 3 hours.
g/c2! Do not keep the autoclave in the lower chamber,
Pre-foaming was performed by opening the lube and releasing the mixture of resin particles and water to atmospheric pressure. The obtained pre-expanded particles had no fusion between particles, were substantially composed of uniform fine closed cells, and had an expansion ratio of 40 times.

比較例1 傾斜角度か全くない、通常のH型攪拌翼を用いて攪拌を
行った他は実施例1と同様な方法で実験を行った。しか
し、オートクレーブ内温を136°Cに加熱昇温後、約
80分でオートクレーブ内の樹脂粒子同志が融着してし
まい攪拌が不能になり予備発泡を行うことはできなかっ
た。
Comparative Example 1 An experiment was conducted in the same manner as in Example 1, except that stirring was performed using a normal H-type stirring blade with no inclination angle. However, after heating the autoclave to 136° C., the resin particles in the autoclave fused together in about 80 minutes, making stirring impossible and making it impossible to perform preliminary foaming.

実施例2〜5.比較例2 45°と変化させた他は実施例1と同様な方法で予備発
泡を行った。結果を表−1に示す。
Examples 2-5. Comparative Example 2 Pre-foaming was carried out in the same manner as in Example 1 except that the angle was changed to 45°. The results are shown in Table-1.

表−1 [ 片 「 火 [− 「 *1 保持後40分で樹脂粒子が融着塊化尚、傾斜角度
が50°の場合には、攪拌力かほとんどなく粒子の融着
を生起し実施不能であった。
Table 1 [ `` fire `` * 1 40 minutes after holding, the resin particles fuse and form a lump. Furthermore, if the inclination angle is 50°, there is almost no stirring force and the particles fuse, making it impossible to carry out the process. Met.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は、本発明の方法に使用する予備発泡用の耐圧容
器の説明図である。第2図は通常のH型攪拌翼、第3図
は本発明の特殊H型攪拌翼を示したものであり、Aは正
面図、Bは側面図である。 示したもので、Aは正面図、Bは側面図である。 1は耐圧容器本体、2は特殊H型撹拌翼を取付けた攪拌
装置、3は特殊■(型撹拌翼、4は加熱用、2ジヤケツ
ト、5はポリオレフィン系樹脂粒子、6は放出用バルブ
。 特許出廓人 鐘淵化学工業株式会社 代理人 弁理士浅野真−
FIG. 1 is an explanatory diagram of a pressure-resistant container for pre-foaming used in the method of the present invention. FIG. 2 shows a normal H-type stirring blade, and FIG. 3 shows a special H-type stirring blade of the present invention, where A is a front view and B is a side view. In the figures, A is a front view and B is a side view. 1 is the pressure-resistant container main body, 2 is a stirring device equipped with a special H-type stirring blade, 3 is a special ■ (type stirring blade), 4 is for heating, 2 is a jacket, 5 is polyolefin resin particles, 6 is a discharge valve. Patent Representative Makoto Asano, Patent Attorney, Kanebuchi Chemical Industry Co., Ltd.

Claims (7)

【特許請求の範囲】[Claims] (1)耐圧容器中で、揮発性発泡剤を含有するポリオレ
フィン系狗脂粒子を水に分散させ、該樹脂粒子の軟化温
度以上の温度に加熱し、該発泡剤の蒸気圧以上の加圧下
で、該粒子と水との混合物を低圧域に放出するポリオレ
フィン系樹脂粒子の予備発泡方法において、該粒子の水
への分散は、分散剤と界面活性剤を使用し、H型攪拌翼
を該攪拌翼の垂直面から攪拌方向側に傾斜させた特殊H
型攪拌翼で撹拌することを特徴とするポリオレフィン系
樹脂粒子の予備発泡方法。
(1) In a pressure-resistant container, polyolefin resin particles containing a volatile foaming agent are dispersed in water, heated to a temperature higher than the softening temperature of the resin particles, and under pressure higher than the vapor pressure of the foaming agent. , a pre-foaming method for polyolefin resin particles in which a mixture of the particles and water is discharged into a low pressure region, in which the particles are dispersed in water using a dispersant and a surfactant, and an H-type stirring blade is used to stir the particles. Special H tilted from the vertical plane of the blade toward the stirring direction
A method for pre-foaming polyolefin resin particles characterized by stirring with a molded stirring blade.
(2)  攪拌方向側に5°〜45°の範囲で傾斜させ
た特殊H型撹拌翼で攪拌する特許請求の範囲第1項記載
のポリオレフィン系樹脂粒子の予備発泡方法。
(2) The method for pre-foaming polyolefin resin particles according to claim 1, which comprises stirring with a special H-type stirring blade tilted in the stirring direction at an angle of 5° to 45°.
(3)撹拌方向側に5°〜30°の範囲で傾斜させた特
殊H型攪拌翼で攪拌する特許請求の範囲第1項記載のポ
リオレフィン系樹脂粒子の予備発泡方法。
(3) The method for pre-foaming polyolefin resin particles according to claim 1, wherein stirring is carried out using a special H-shaped stirring blade tilted in the stirring direction at an angle of 5° to 30°.
(4)撹拌方向側に5°〜20°の範囲で傾斜させた特
殊H型攪拌翼で攪拌する特許請求の範囲第1項記載のポ
リオレフィン系樹脂粒子の予備発泡方法。
(4) The method for pre-foaming polyolefin resin particles according to claim 1, wherein stirring is carried out using a special H-type stirring blade tilted at an angle of 5° to 20° in the stirring direction.
(5)  分散剤は第3リン酸カルシウムであり、その
使用量はポリオレフィン系樹脂粒子100重量部に対し
0.05〜1.0重量部である特許請求の範囲第1項記
載のポリオレフィン系樹脂粒子の予備発泡方法。
(5) The dispersant is tertiary calcium phosphate, and the amount used is 0.05 to 1.0 parts by weight per 100 parts by weight of the polyolefin resin particles. Pre-foaming method.
(6)界面活性剤はドデシルベンゼンスルーホン酸ンー
タ、又はn−パラフィンスルホン酸ソーダであり、その
使用量はポリオレフィン系樹脂粒子100重量部に対し
0.001〜0.05重量部である特許請求の範囲第1
項記載のポリオレフィン系樹脂粒子の予備発泡方法。
(6) A patent claim in which the surfactant is dodecylbenzene sulfonate or sodium n-paraffin sulfonate, and the amount used is 0.001 to 0.05 parts by weight per 100 parts by weight of the polyolefin resin particles. range 1
A method for pre-foaming polyolefin resin particles as described in 1.
(7)  ポリオレフィン系樹脂が、低密度ポリエチレ
ン、中密度ポリエチレン、高密度ポリエチレン、直鎖状
低密度ポリエチレン、ポリプロピレン、エチレン−プロ
ピレンランダムコポリマー、エチレン−プロピレンブロ
ックコポリマー、エチレン−酢酸ビニルコホリマーから
なる群から選ばれる1権又は2種以上の混合樹脂である
特許請求の範囲第1項記載のポリオレフィン系樹脂粒子
の予備発泡方法。
(7) The polyolefin resin is selected from the group consisting of low density polyethylene, medium density polyethylene, high density polyethylene, linear low density polyethylene, polypropylene, ethylene-propylene random copolymer, ethylene-propylene block copolymer, and ethylene-vinyl acetate copolymer. The method for pre-foaming polyolefin resin particles according to claim 1, wherein the polyolefin resin particles are one or more mixed resins.
JP58047683A 1983-03-22 1983-03-22 Pre-expansion of polyolefin resin particle Granted JPS59172532A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58047683A JPS59172532A (en) 1983-03-22 1983-03-22 Pre-expansion of polyolefin resin particle

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58047683A JPS59172532A (en) 1983-03-22 1983-03-22 Pre-expansion of polyolefin resin particle

Publications (2)

Publication Number Publication Date
JPS59172532A true JPS59172532A (en) 1984-09-29
JPH0446976B2 JPH0446976B2 (en) 1992-07-31

Family

ID=12782071

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58047683A Granted JPS59172532A (en) 1983-03-22 1983-03-22 Pre-expansion of polyolefin resin particle

Country Status (1)

Country Link
JP (1) JPS59172532A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01301210A (en) * 1988-05-30 1989-12-05 Kanegafuchi Chem Ind Co Ltd Prefoaming device for thermoplastic synthetic resin particles
WO2002100929A1 (en) * 2001-06-11 2002-12-19 Jsp Corporation Method for producing polypropylene type resin foamed particle
JP2010053274A (en) * 2008-08-29 2010-03-11 Kaneka Corp Method for producing polyolefin-based resin foamed particles, and polyolefin-based resin foamed particles and in-mold expansion molded articles formed by the same
US11498247B2 (en) 2016-07-06 2022-11-15 Kaneka Corporation Foaming particle manufacturing device using polyolefin-based resin particle and method for manufacturing said foaming particle

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20230386079A1 (en) 2022-05-31 2023-11-30 Konica Minolta, Inc. Impression analysis system, impression analysis method, and recording medium

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50127968A (en) * 1974-03-28 1975-10-08
JPS5138746A (en) * 1974-09-27 1976-03-31 Obayashi Constr Co Ltd
JPS52134672A (en) * 1976-05-04 1977-11-11 Kanegafuchi Chemical Ind Process for manufacture of expandable thermoplastic polymer powder
JPS5833435A (en) * 1981-08-24 1983-02-26 Japan Styrene Paper Co Ltd Preparation of pre-foamed particles
JPS6418331U (en) * 1987-07-17 1989-01-30

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS50127968A (en) * 1974-03-28 1975-10-08
JPS5138746A (en) * 1974-09-27 1976-03-31 Obayashi Constr Co Ltd
JPS52134672A (en) * 1976-05-04 1977-11-11 Kanegafuchi Chemical Ind Process for manufacture of expandable thermoplastic polymer powder
JPS5833435A (en) * 1981-08-24 1983-02-26 Japan Styrene Paper Co Ltd Preparation of pre-foamed particles
JPS6418331U (en) * 1987-07-17 1989-01-30

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01301210A (en) * 1988-05-30 1989-12-05 Kanegafuchi Chem Ind Co Ltd Prefoaming device for thermoplastic synthetic resin particles
WO2002100929A1 (en) * 2001-06-11 2002-12-19 Jsp Corporation Method for producing polypropylene type resin foamed particle
US6838488B2 (en) 2001-06-11 2005-01-04 Jsp Corporation Production method of foamed polypropylene resin beads
JP2010053274A (en) * 2008-08-29 2010-03-11 Kaneka Corp Method for producing polyolefin-based resin foamed particles, and polyolefin-based resin foamed particles and in-mold expansion molded articles formed by the same
US11498247B2 (en) 2016-07-06 2022-11-15 Kaneka Corporation Foaming particle manufacturing device using polyolefin-based resin particle and method for manufacturing said foaming particle

Also Published As

Publication number Publication date
JPH0446976B2 (en) 1992-07-31

Similar Documents

Publication Publication Date Title
US4436840A (en) Process for producing pre-foamed particles of polyolefin resin
US4704239A (en) Process for the production of expanded particles of a polymeric material
EP0095109A1 (en) Process for producing expanded particles of a polyolefin resin
EP0123816B1 (en) Pre-expanded particle of polyolefin and process for preparing the same
US4761431A (en) Pre-expanded particles of propylene resin
US4602047A (en) Process for producing foamed particles of polyolefin resin
JPS6215239A (en) Uncrosslinked straight chain low-density polyethylene preexpanded partifle and molding thereof
JPH082989B2 (en) Pre-expansion method of polyolefin resin particles
JPS59172532A (en) Pre-expansion of polyolefin resin particle
JPH072856B2 (en) Polyolefin foamed particles and method for producing the same
US5380766A (en) Process for the preparation of prefoamed polyolefin particles
JP2000044717A (en) Pre-expanded polypropylene resin particle, and production of in-mold foamed molding therefrom
JPH0428738B2 (en)
JPH0446977B2 (en)
JP2001226513A (en) Polyolefin foam particle having high-density surface layer and its preparation method
JPS59147029A (en) Preparation of expanded particles of polyethylene having uniform and fine bubbles
JPH07116314B2 (en) Method for producing foamed polymer molded article
JPS62177038A (en) Production of pre-expanded particle of thermoplastic resin
JPH04351646A (en) Production of preexpanded particle
JP3126171B2 (en) Method for producing expanded polyolefin resin particles
JPH09124832A (en) Polyloefin-based resin preliminary foamed particle and its production
JPH0554855B2 (en)
JPH0322411B2 (en)
JPH0314845A (en) Preparation of pre-expanded bead of polyolefin resin
JPS6234334B2 (en)