JPS58168626A - Production of spherical polypropylene resin particle - Google Patents

Production of spherical polypropylene resin particle

Info

Publication number
JPS58168626A
JPS58168626A JP5176582A JP5176582A JPS58168626A JP S58168626 A JPS58168626 A JP S58168626A JP 5176582 A JP5176582 A JP 5176582A JP 5176582 A JP5176582 A JP 5176582A JP S58168626 A JPS58168626 A JP S58168626A
Authority
JP
Japan
Prior art keywords
particles
resin particles
polypropylene resin
spherical
resin
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
JP5176582A
Other languages
Japanese (ja)
Other versions
JPH032890B2 (en
Inventor
Hideki Kuwabara
英樹 桑原
Shohei Yoshimura
吉村 正平
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 JP5176582A priority Critical patent/JPS58168626A/en
Publication of JPS58168626A publication Critical patent/JPS58168626A/en
Publication of JPH032890B2 publication Critical patent/JPH032890B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To produce spherical PP resin particles capable of providing pre- expanded particles of a uniform shape, by dispersing PP resin particles in a dispersing medium with the aid of a specified dispersant and then heating the dispersion. CONSTITUTION:100pts.wt. PP resin particle having a weight below 6mg per particle and above 0.4pts.wt. at least one dispersant selected from the group consisting of basic magnesium carbonate, talc and Al2O3 are dispersed in at least 100pts.wt. dispersing medium (e.g., water), and maintained for at least 15min under agitation at temperatures ranging from the m.p. of the resin particles >=10 deg.C to the m.p. <=50 deg.C.

Description

【発明の詳細な説明】 本発明は球状ポリプロピレン系樹脂粒子OIl造方法に
関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing spherical polypropylene resin particles OIl.

従来よ)発池成臘体は、ポリスチレン、架橋ポリエチレ
ンを材質として例えと予備発泡粒子を用いるビーズ威臘
法等Kjllll造されている。一方。
Conventionally, foamed bodies have been manufactured using polystyrene, cross-linked polyethylene as materials, and the bead molding method using pre-expanded particles. on the other hand.

本出願入れポリプロピレン系樹脂が機械的強度。The polypropylene resin used in this application has mechanical strength.

耐熱性、耐薬品性、耐油性等が優れていることからその
発池威臘体の開発O研究を進め九結果、予備II&鋤稼
子を得る方tcsI−よびその予備発泡粒子を用いて発
―虞m件を得る方法の一尭に成功し、すでKm案してi
る。
Due to its excellent heat resistance, chemical resistance, oil resistance, etc., we have conducted research on the development of the foamed material, and as a result, we have developed a method for obtaining pre-expanded particles using tcsI- and its pre-expanded particles. - I have succeeded in finding a way to obtain the information, and have already made plans for Km.
Ru.

しかしながら、ポリスチレンが懸濁重合法によシ、を九
ポリエチレンが架橋工程によ〉球状の樹1IIII子を
得ることがで龜、その樹rtr較子を用いて得られる予
備発泡粒子が球状となるのに対し、ポリプロピレン系樹
脂の、場合に紘、無架橋anti粒  j子を用いて予
備発泡粒子が得られる反両、lIられる予備発泡粒子#
i掬−な球状のものが得られ難く・その予備発泡粒子紘
虞置用金臘に効率的に充填し難い丸め均−e尭池威臘体
を得られ難い点で未だ改良の金地を残しているものであ
る。
However, when polystyrene is produced by the suspension polymerization process, it is possible to obtain spherical particles using the crosslinking process, and the pre-expanded particles obtained using the RTR process are spherical. On the other hand, pre-expanded particles can be obtained using non-crosslinked anti-particles of polypropylene resin.
It is difficult to obtain a scooped spherical shape, and it is difficult to efficiently fill the container for storing the pre-foamed particles, and it is difficult to obtain a rounded, uniform shape, so there is still room for improvement. It is something that

本発llj社上記従来技術の欠点を簿消した球状ポリプ
ロピレン系樹脂粒子の製造方法を提供することを目的と
するもOであって2本幾羽者ら紘、上記目的tagすべ
く鋭意研究した結果 *脂粒子を、塩基銖炭朧マグネシ
ウム、タルタ壜た紘蒙化アに電ニウムある%A紘それら
の鼻金物からなる分を薄を用いて分散111に分散し*
1lIll脂粒子O融点+10℃以上の温度に加熱する
ことによって球状のポリプルピレン系樹脂が得られるこ
とを見出し。
The purpose of this project is to provide a method for producing spherical polypropylene resin particles that eliminates the drawbacks of the above-mentioned conventional technology. Result *The fat particles were dispersed in 111% using a diluted base of magnesium, a tarta bottle, and an electrolyte in a tartar bottle.*
It has been discovered that a spherical polypropylene resin can be obtained by heating to a temperature of 1lIll fat particle O melting point + 10°C or higher.

本発明を完成するに至っ良。The present invention is now complete.

すなわち1本発明はポリプロピレン系樹脂粒子を、#樹
脂粒子100重量部に対して塩基性炭酸マグネシウム、
タルク、酸化アルンニクム01種または2種以上からな
る分散剤04重量部以上を用いて分散媒に分散し、上記
樹脂粒子の融点+10℃以上0I11度に加熱すること
を特徴とする球状ポリプロピレジ系樹脂粒子の製造方法
を特旨とするものである。
That is, 1 the present invention uses polypropylene resin particles, basic magnesium carbonate,
A spherical polypropylene resin resin characterized by being dispersed in a dispersion medium using 4 parts by weight or more of a dispersing agent consisting of 01 type or 2 or more types of talc and alunnicum oxide, and heated to 11 degrees above the melting point of the resin particles +10 degrees Celsius. This paper focuses on a method for producing particles.

本li−において、ポリプロピレン系*、W*子の材質
としてa、Sえ杖プロピレン単独重金体、エチレンーグ
ロビレンツンダム共重6体、エチレン−プロピレンブロ
ック共重合体等が挙ぜられ、これら紘単独まえは混合し
て用いることができるが。
In this li-, materials for the polypropylene system* and W* child include a, propylene monoheavy metal, ethylene-globylene-sundum copolymer 6, ethylene-propylene block copolymer, etc. Hiro can be used alone or in combination.

エチレン−プロピレンランダム共重合体が41に好まし
い。tえ、ポリプロピレン系llll11子は押出機゛
によりベレット化し良もOe l)砕機にて看砕したも
の等を用いることができ、そoh状紘とOよう傘もので
もよいが、この樹脂粒子O重量れ6mg/個以下、好ま
しくは15m17個以下が好ましい。
Ethylene-propylene random copolymer is preferred for 41. In addition, polypropylene resin particles can be made into pellets using an extruder or milled using a crusher. The weight is preferably 6 mg/piece or less, preferably 15m17 pieces or less.

本発明において、用いることができる分散剤紘。A dispersant that can be used in the present invention.

塩基性炭酸!グネシウ^、タルタまたは酸化アル1=ウ
ムのうちのill壕九はそれらの2種以上の渦金物であ
る。この分散剤はポリプロピレン系樹脂粒子100重量
部に対し0.4重量部以上用いる。
Basic carbonic acid! The illumination of Gnesium, Tarta, or Aluminum oxide is a combination of two or more of them. This dispersant is used in an amount of 0.4 parts by weight or more per 100 parts by weight of the polypropylene resin particles.

分散能の添加量が0.4重量部未満の場金に紘1本発−
の目的である樹脂粒子の球形化が期待できない。を製分
散剤として、前記し丸もの以外のもの例えば、塩基性炭
酸亜鉛、リン酸カルシウム、及び炭酸カルシウム等を使
用しても球形化の効果は全く望めない。但し、これらの
分散剤も本発明の効果を阻害しない範−で添加すること
紘訪ぜるものでない。を九樹脂較子が分散される分散媒
としては2例えば水、エチレングリコール、ダリセリン
、メタノール、エタノール等のうちの1種また紘それら
の2種以上01&会物等が挙けられるが過    f當
は水が好ましい。分散媒の使用量は通常樹脂粒子100
重量部に対し100重量部以上である。
If the added amount of dispersion ability is less than 0.4 parts by weight, please use Koichimoto.
It cannot be expected to make the resin particles spherical, which is the purpose of this method. Even if substances other than the above-mentioned round ones, such as basic zinc carbonate, calcium phosphate, and calcium carbonate, are used as a dispersant, no effect of spheroidization can be expected. However, these dispersants may not be added as long as they do not impede the effects of the present invention. Examples of the dispersion medium in which the resin is dispersed include one of water, ethylene glycol, dalycerin, methanol, ethanol, etc., and two or more of these. Water is preferred. The amount of dispersion medium used is usually 100 resin particles.
The amount is 100 parts by weight or more.

本発wAにおいて、樹It’s千紘該樹脂誼子の融点+
10℃以上の温度、好ましくは融点+12℃以上から融
点+50℃以下011111に加熱される。加熱11f
が11点+10℃未満の場金ecalllll11子の
球形化が困難で6i本薙@0@的を達成することができ
ない。オ九加熱温臘が所望の温度に胸達し九後15分以
上保持することが好ましい。
In this wA, it's Chihiro's melting point +
It is heated to a temperature of 10°C or higher, preferably from melting point +12°C or higher to melting point +50°C or lower. heating 11f
If the temperature is less than 11 points + 10 degrees Celsius, it is difficult to make the 11 particles spherical, and it is impossible to achieve the 6i Honnagi@0@target. After heating reaches the desired temperature, it is preferable to hold the temperature for at least 15 minutes.

本発@において、樹脂粒子OIk点の調定は示差走査熱
量分析(D8C)Kよって行なつえ。こemit定法で
紘、試料セット後窒素雰囲気にて10℃/分の適度で2
00℃まで昇温し、七〇4110℃/分で50℃まで降
温し、再[10℃/分で昇温し九ときの融解ピークの頂
点を融点とし、ビータが複数の場金はその平均温度を融
点とし丸。
In this publication, the resin particle OIk point is determined by differential scanning calorimetry (D8C). After setting the sample, heat at a moderate rate of 10°C/min in a nitrogen atmosphere.
Raise the temperature to 00℃, lower the temperature to 50℃ at a rate of 704110℃/min, and then increase the temperature again at a rate of 10℃/min. A circle with temperature as the melting point.

本発明によシ得られる球状ポリプロピレン系樹脂粒子は
9例えばam樹脂の予備発泡粒子の製造に有効に用いる
ことができる。この予備発泡粒子の製造方法は例えば 
*m審器内K1m1脂聴子、揮斃性発泡剤2分散媒を入
れ、攪拌下、所定温度に昇温し、容器内の圧力を揮発性
発泡剤の蒸気圧以上1え紘以下の圧力に41持しながら
容器の一端を−放し、樹脂粒子と分散媒とを同時に容器
内より低圧の雰囲気に款出することKjり行なわれる。
The spherical polypropylene resin particles obtained according to the present invention can be effectively used for producing pre-expanded particles of, for example, am resin. This pre-expanded particle manufacturing method is, for example,
*Pour K1ml of volatile blowing agent and 2 dispersion medium into the container, raise the temperature to the specified temperature while stirring, and reduce the pressure inside the container to a pressure that is greater than or equal to the vapor pressure of the volatile foaming agent and less than 1. One end of the container is released while holding the container for 41 minutes, and the resin particles and dispersion medium are simultaneously pumped out from inside the container into a lower pressure atmosphere.

このようにして得られる予備発泡粒子は粒子形状のバラ
ツキが少なく、を大気泡径(気池歇)のバラツキも少な
いものである。まえ予備発泡粒子製造時に紘、通常2分
散剤が用いられ、予備発泡粒子を得た後そこに付着した
分散剤を洗浄除去して−るが1本発WAKよ)得られる
樹脂粒子を用いれば、予備発泡粒子を洗浄する必l!紘
なく、また予備発泡粒子製造時、書閉容器内に残音する
樹脂粒子も非霊に少なくなる。
The pre-expanded particles thus obtained have less variation in particle shape and less variation in the diameter of the air bubbles. When producing pre-expanded particles, usually two dispersants are used, and after obtaining the pre-expanded particles, the dispersant adhering to them is washed away, but if the resulting resin particles are used , it is necessary to wash the pre-foamed particles! There is no noise, and the number of resin particles that remain in the closed container during the production of pre-expanded particles is also significantly reduced.

を九上記のようにして得られ九予備発泡粒子を用いて発
泡威履体を・得ることができ、この予備発泡粒子O形状
は均一なので威渥用金111に効率的に充填で亀、まえ
気fIIAllのバラツキも少ないので均一な優れ丸物
性を有する発池威渥体を得ることができる。
A foamed shoe body can be obtained using the pre-expanded particles obtained as described above, and since the shape of the pre-expanded particles is uniform, the foaming material 111 can be efficiently filled into the foam body. Since there is little variation in the temperature, it is possible to obtain a spring-loaded body having uniform and excellent round physical properties.

以上1111iL九ように本発@によれ鑓、塩基性炭酸
!グネシウム、タル!、酸化アル建ニウムの1atたは
2種以上からなる分散剤を樹脂粒子100重量部に対し
て0.4重量部以上用いて樹脂掌子の融点+10℃以上
の温度に樹脂粒子を加熱する仁とによ〕球状の樹脂粒子
を得ることができ、この球状の樹脂粒子を例えば予備発
泡粒子の製造に用い良場合、形状、気泡径等が均一な予
備発泡粒子を得ることができ、さらに紘こO予備発泡粒
子を用いて得られる発池威瀝体は優れた物性を有するも
のである等の利点を有するものである。
Above 1111iL 9, this is the main carbonic acid, basic carbonic acid! Gnesium, Tal! , a process in which resin particles are heated to a temperature higher than the melting point of the resin base + 10°C using 0.4 parts by weight or more per 100 parts by weight of resin particles of a dispersant consisting of 1at or 2 or more types of aluminum oxide. If it is possible to obtain spherical resin particles, and if these spherical resin particles are used, for example, in the production of pre-expanded particles, it is possible to obtain pre-expanded particles with uniform shape, cell diameter, etc. The expanded body obtained using the O pre-expanded particles has advantages such as excellent physical properties.

以下、実施例および比較例を搗けて本発明をさらに詳1
1に説明する。
Hereinafter, the present invention will be explained in further detail by reviewing Examples and Comparative Examples.
I will explain in 1.

実施例1〜9および比較例1〜3 5ノのオートクレーブKJII表に示すポリプレピレン
系樹脂粒子1分散剤および水を入れ、攪拌下。
Examples 1 to 9 and Comparative Examples 1 to 3 Polypropylene resin particles 1 shown in the KJII table 1 dispersant and water were added to an autoclave with stirring.

153〜180℃の温度に加熱して1時間保持し丸。得
られた樹脂粒子の形状を観察し良。肯1本実施例及び比
較例で使用するポリプロピレン系樹脂の融点紘以下の過
)である。
Heat to a temperature of 153-180°C and hold for 1 hour. Observe the shape of the obtained resin particles. (1) The melting point of the polypropylene resin used in these Examples and Comparative Examples is below.

ポリプロピレン系樹脂       融A (’C)プ
ルピレン単独重合体       16sエチレン−ブ
ーピレンランダム共重合体  145エチレン−プロピ
レンブロック共重合体  163結果tal1表に示す
Polypropylene Resin Melt A ('C) Propylene Homopolymer 16s Ethylene-Boopylene Random Copolymer 145 Ethylene-Propylene Block Copolymer 163 The results are shown in Table tal1.

更に、実施例3で得られ丸球状粒子を嬉1図に。Furthermore, the round spherical particles obtained in Example 3 are shown in Figure 1.

比較例1及び2で得られ九粒子をそれぞれ112図及び
31311に示す。
Nine particles obtained in Comparative Examples 1 and 2 are shown in Figures 112 and 31311, respectively.

実施例1Oおよび比較例6〜7 s10オートクレーブKm施例3で得られIL樹脂較子
まえは熱鶏履していない樹脂粒子10.00j。
Example 1O and Comparative Examples 6-7 s10 Autoclave Km 10.00j of IL resin particles obtained in Example 3 and not heated before heating.

ジクロロシフ四pメタン20077、塩!性脚駿マグネ
シウム1lliII(実施例10は使用せず)および水
5oooIを入れ、容器の一端を−放し、容器内の圧力
をs skp/ai1mlを145℃に保持しながら予
備ll池を行なり友。得られた予備発泡粒子の形状、気
11s状のバラツキを測定し。
Dichlorosifu 4p methane 20077, salt! Add 1lliII of magnesium (Example 10 was not used) and 5oooI of water, release one end of the container, and conduct a preparatory cycle while maintaining the pressure inside the container at 145°C. . The shape of the obtained pre-expanded particles was measured for variations in shape.

を友オートクレーブ中に残留する樹脂粒子の量を測定し
良。結果を11128に示す。
Measure the amount of resin particles remaining in the autoclave. The results are shown in 11128.

tた得られえ予備発泡粒子を威履用金履に充填し、加熱
、尭池させて尭池威瀝体を得友。威m時O威履性を調べ
九。結果を菖2111EK併せて示す。
The obtained pre-expanded particles are filled into metal shoes for wear, heated and allowed to cool to form a cool body. Examine the power and power characteristics.9. The results are also shown for Iris 2111EK.

陶、実施例10で得られた予備発泡粒子を嬉412に!
びに比較例6及び7で得られ九予備発泡粒子なそれぞれ
JIS園及び第6図に示す。
Pottery, the pre-expanded particles obtained in Example 10 are made into 412!
The nine pre-expanded particles obtained in Comparative Examples 6 and 7 are shown in JIS Encyclopedia and FIG. 6, respectively.

*1−気泡径のバラツキ紘下記の如く判定し良。*1-Variation in bubble diameter: Good as determined as below.

嘗子閤および種子内0バラツキなし     。There is no variation within the seeds.

粒子間また紘粒子内のいずれかバッツ命有〉   Δ籾
子閤および数子内いずれもバッツ中有jI     x
※2−樹脂軸子のオートクレーブ内真冑状態紘下記O如
く判定しえ。
Either between the particles or within the particles, there is a Bats life.〉 Both inside the rice grains and Kazuko, there are Bats insides jI x
*2 - Determine the true state of the resin shaft in the autoclave as shown in O below.

幾奮樹**子が全41Iilfi1粒子03憾未満  
    。
Ikubuki** child is less than 41 Iilfi 1 particle 03 regrets
.

I    3嚢以上10悌未満   Δ10憾以上  
  × 秦!−@子廖状0バ2ツ中紘、岡秦件にてIo−予備発
泡したと會0壺ロフト関□バッッキによp下記の如<4
11定し良。
I 3 capsules or more and less than 10 capsules Δ10 capsules or more
× Qin! -@子廖形 0 BA 2 TSU Nakahiro, Io in the Okahata case - Pre-foaming and meeting 0 jar loft Seki □ Bacchi as below < 4
11 fixed.

都−以上同じものQ @〜7@肯じ%OΔ 5回以下同じもの      × *4−成臘性は下記O如く判定し良。Miyako - Same as above Q @〜7@agree%OΔ Same thing 5 times or less × *4-Successibility is determined as O below.

zs#/j(G)以下の水蒸気にて    0社着する
もの L S Ill/j (G)以上の*1mで*hと  
×融着しないもの *5−威擺性紘1011威履し良ときの優嵐品のIl数
によ)判定しえ。
zs#/j (G) or less water vapor reaches 0 company L S Ill/j (G) or more *1m with *h
×Items that do not fuse *5 - Determine based on the Il number of the Yuran product when it is worn.

9鋼以上       0 6個以下       × 4、間両の簡単なIIWA J111I紘本尭明によ)得られ大樹脂粒子を示す斜視
If、 8211シよび111311は本発明以外の方
法によ)得られ大樹脂粒子を示す斜視図、 jlE4I
IIは本m−によ〉得られ大樹脂粒子を用−て調造され
た予備薙池和子を示す斜*Sa、菖5図および第6、、
□□。、えよ4.t、□1□、   “用いて調造され
た予備尭池較子を示す斜lll1llで6る。
9 steel or more 0 6 or less × 4, simple IIWA J111I (according to Takaaki Hiromoto) Obtained large resin particles If, 8211 and 111311 are obtained by methods other than the present invention) A perspective view showing resin particles, jlE4I
II shows preliminary Kazuko Nagiike prepared using large resin particles obtained according to this book M-Sa, iris 5 and 6,
□□. , Eyo 4. t, □1□, 6 with the diagonal lll1ll showing the reserve prepared using.

第1図 第2図 第3図 第4図 第5図 第6図 手続補正書(麿斃) 昭和s1年sり!3日 特許庁長官島 調 春 樹殿 1、事件の表示 曙和1f年411?IIIjl  8116m  12
、 発明の名称球状ポ讐1■ピレン系樹脂載子・劇造方
論3、 補正をする者 事件との関係   轡許出願人 住 所東京・千代田区内中町3丁I重書1勺氏 名(名
称)lI本スチレンペーパー株式会社代表者 長  W
*   會 4・代理人〒1・1 5、補正命令の日付    −一補正 8、補正の内容    嬉畠閣を別紙・過−補正する。
Fig. 1 Fig. 2 Fig. 3 Fig. 4 Fig. 5 Fig. 6 Procedural amendment (Maro) Showa S1 sri! 3rd Patent Office Commissioner Shima Cho Haru Judono 1, Incident Display Akebono 1f 411? IIIjl 8116m 12
, Title of the invention: Spherical Potion 1 ■ Pyrene-based resin layer/gekisou method theory 3, Relationship with the case of the person making the amendment Address of the applicant: 3-I Jusho, 3-chome, Uchinaka-cho, Chiyoda-ku, Tokyo Name (Name) II Honstyrene Paper Co., Ltd. Representative W.
* Meeting 4/Agent 〒1/1/5, Date of amendment order -1 Amendment 8, Contents of amendment Kikihakaku is attached and over-amended.

第3図Figure 3

Claims (1)

【特許請求の範囲】 ポリプロピレン系樹脂粒子を、該樹11較子io。 重量部に対して塩基性炭酸マダネシクム、メルク。 酸化アルミニウムのlslまえは2種以上からなる分散
剤04重量部以上を用いて分散媒に分散し。 上記樹*si子の融点+10℃以上の1lllK加熱す
ることVt411黴とする球状ポリプロピレン系樹脂粒
子OS造方法。
[Claims] The polypropylene resin particles are made of polypropylene resin particles. Parts by weight: Madanesicum basic carbonate, Merck. Before aluminum oxide is used, it is dispersed in a dispersion medium using 4 parts by weight or more of a dispersant consisting of two or more types. A method for producing an OS of spherical polypropylene resin particles, in which Vt411 mold is produced by heating the above-mentioned resin at 111K above the melting point of +10°C.
JP5176582A 1982-03-30 1982-03-30 Production of spherical polypropylene resin particle Granted JPS58168626A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5176582A JPS58168626A (en) 1982-03-30 1982-03-30 Production of spherical polypropylene resin particle

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5176582A JPS58168626A (en) 1982-03-30 1982-03-30 Production of spherical polypropylene resin particle

Publications (2)

Publication Number Publication Date
JPS58168626A true JPS58168626A (en) 1983-10-05
JPH032890B2 JPH032890B2 (en) 1991-01-17

Family

ID=12896040

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5176582A Granted JPS58168626A (en) 1982-03-30 1982-03-30 Production of spherical polypropylene resin particle

Country Status (1)

Country Link
JP (1) JPS58168626A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60221440A (en) * 1984-04-19 1985-11-06 Badische Yuka Co Ltd Production of foamed particles of propylene resin
JPS60245649A (en) * 1984-05-19 1985-12-05 Japan Styrene Paper Co Ltd Preparation of foamed particle of crosslinked polyolefin resin

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7956513B2 (en) 2007-04-20 2011-06-07 Mitsumi Electric Co., Ltd. Method of driving a driving device
JP5845292B2 (en) * 2014-01-14 2016-01-20 株式会社ジェイエスピー POLYOLEFIN RESIN PARTICLE, POLYOLEFIN RESIN FOAM PARTICLE AND METHOD FOR PRODUCING POLYOLEFIN RESIN FOAM PARTICLE

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60221440A (en) * 1984-04-19 1985-11-06 Badische Yuka Co Ltd Production of foamed particles of propylene resin
JPH0525892B2 (en) * 1984-04-19 1993-04-14 Mitsubishi Yuka Baadeitsushe Kk
JPS60245649A (en) * 1984-05-19 1985-12-05 Japan Styrene Paper Co Ltd Preparation of foamed particle of crosslinked polyolefin resin
JPH0464331B2 (en) * 1984-05-19 1992-10-14 Jsp Corp

Also Published As

Publication number Publication date
JPH032890B2 (en) 1991-01-17

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