JP2869475B2 - Method for producing polyolefin foam - Google Patents
Method for producing polyolefin foamInfo
- Publication number
- JP2869475B2 JP2869475B2 JP4351625A JP35162592A JP2869475B2 JP 2869475 B2 JP2869475 B2 JP 2869475B2 JP 4351625 A JP4351625 A JP 4351625A JP 35162592 A JP35162592 A JP 35162592A JP 2869475 B2 JP2869475 B2 JP 2869475B2
- Authority
- JP
- Japan
- Prior art keywords
- foam
- cooling
- mold
- polyolefin
- cross
- 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.)
- Expired - Lifetime
Links
- 239000006260 foam Substances 0.000 title claims description 73
- 229920000098 polyolefin Polymers 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 238000001816 cooling Methods 0.000 claims description 46
- 239000004088 foaming agent Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 239000003431 cross linking reagent Substances 0.000 claims description 8
- 238000000034 method Methods 0.000 description 20
- 238000005187 foaming Methods 0.000 description 17
- 238000010438 heat treatment Methods 0.000 description 15
- 238000000465 moulding Methods 0.000 description 11
- 239000000047 product Substances 0.000 description 7
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 5
- 238000000748 compression moulding Methods 0.000 description 5
- 239000002826 coolant Substances 0.000 description 4
- 229910052751 metal Chemical class 0.000 description 4
- 239000002184 metal Chemical class 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 239000000498 cooling water Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000012467 final product Substances 0.000 description 3
- 239000003507 refrigerant Substances 0.000 description 3
- 235000014692 zinc oxide Nutrition 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 2
- 239000004156 Azodicarbonamide Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 2
- 235000019399 azodicarbonamide Nutrition 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000010097 foam moulding Methods 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 229910000464 lead oxide Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Landscapes
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、ポリオレフィン発泡体
の製造方法に関し、更に詳しくは、2段発泡法において
エネルギーロスを減らし、効率良く、表面が平滑で、且
つ縦、横及び高さ方向の寸法均一性に優れたポリオレフ
ィン発泡体の製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a polyolefin foam, and more particularly, to a two-stage foaming method in which energy loss is reduced, the surface is smoothed efficiently, and the height, width and height are reduced. The present invention relates to a method for producing a polyolefin foam having excellent dimensional uniformity.
【0002】[0002]
【従来の技術】ポリオレフィン発泡体の製造方法として
は、ポリオレフィン樹脂、架橋剤及び発泡剤の混和物を
金型内に充填し、加圧、加熱状態でその架橋剤、発泡剤
を完全に分解し、その後、除圧することにより、この混
和物を一度に所望の密度に膨張させて最終発泡体を得る
方法(以下、1段発泡法という。)が知られている。ま
た、特公平2−42649号公報等に開示されている如
く、混和物を一次金型に充填し、加圧下で加熱して発泡
剤の15〜60%を分解することにより1次膨張させ、
その後、その中間発泡体を常圧で加熱し、残余の発泡剤
を分解させて二次膨張させ、所望密度の最終発泡体を得
る方法(以下、2段発泡法という。)も知られている。2. Description of the Related Art As a method for producing a polyolefin foam, a mixture of a polyolefin resin, a crosslinking agent and a blowing agent is filled in a mold, and the crosslinking agent and the blowing agent are completely decomposed under pressure and heat. Then, a method is known in which the mixture is expanded at a time to a desired density by depressurizing to obtain a final foam (hereinafter, referred to as a one-stage foaming method). Further, as disclosed in Japanese Patent Publication No. 42649/1990, the mixture is filled in a primary mold, heated under pressure to decompose 15 to 60% of the foaming agent, and thereby primary expanded,
Thereafter, a method of heating the intermediate foam at normal pressure to decompose the remaining foaming agent and secondary expand to obtain a final foam having a desired density (hereinafter, referred to as a two-stage foaming method) is also known. .
【0003】しかし、上記1段発泡法で高発泡体を得る
場合は、一度に所望密度の最終発泡体に膨張させるた
め、得られる最終発泡体に変形が生じたり、また、金型
から取り出す際、その発泡体に割れが生じたりして、そ
の製品化率が極めて低くなるという問題があった。その
ため、上記2段発泡法が上記1段発泡法の製品化歩留り
の低下を改善すべく開発された。この2段発泡法では、
所定の発泡倍率の製品を一度に発泡膨張させずに、2段
階に分けて発泡膨張させることで、割れ等の製品化歩留
りを低下させる要因を除いている。However, when a high-foamed product is obtained by the above-described one-stage foaming method, the foam is expanded to a final foam having a desired density at one time. In addition, there is a problem that the foam is cracked or the like, and the commercialization rate is extremely low. Therefore, the two-stage foaming method has been developed in order to improve the reduction in the production yield of the one-stage foaming method. In this two-stage foaming method,
A product having a predetermined expansion ratio is expanded and expanded in two stages without expanding and expanding all at once, thereby eliminating factors such as cracks and the like that lower the product production yield.
【0004】しかし、この2段発泡法においても、最終
発泡体の表面平滑性の点で充分とはいえない。従って、
この対策として、特開昭61−266441号公報に述
べている如く、第2発泡工程終了後の発泡体を温熱時に
取り出し、冷却板(特開昭61−266441号公報の
表現では加熱板となっているが、発泡体の温度から見た
場合、その機能としては冷却板といえる。)に挟んで冷
却成形する方法が知られている。[0004] However, even in this two-stage foaming method, the surface smoothness of the final foam is not sufficient. Therefore,
As a countermeasure, as described in JP-A-61-266441, the foam after completion of the second foaming step is taken out at the time of warming, and the cooling plate (in the expression of JP-A-61-266441, becomes a heating plate). However, from the viewpoint of the temperature of the foam, its function can be said to be a cooling plate.
【0005】[0005]
【発明が解決しようとする課題】しかし、特開昭61−
266441号公報の方法で冷却成形した場合、冷却板
による発泡体の圧縮により厚さ方向は均一になるものの
その側方部に応力がかかり、特にその中央部分を中心と
して膨らみが発生するという欠点がある。更に、このよ
うな状態で冷却セットされた発泡体は、発泡体の組織が
上記膨らみ部分(側面中央部分)へ引っぱられる如く歪
をもった状態でセットされている為、経時により発泡体
の4隅部分に凹部(以下、ヒケという。)が発生する。However, Japanese Patent Application Laid-Open No.
In the case of cooling and molding by the method of 266441, the thickness direction becomes uniform due to the compression of the foam by the cooling plate, but stress is applied to the side portion, and particularly, a bulge occurs around the center portion. is there. Furthermore, since the foam which is cooled and set in such a state is set in a state where the structure of the foam is distorted so as to be pulled toward the above-mentioned bulging portion (central portion of the side surface), the foam 4 A concave portion (hereinafter referred to as sink mark) is generated at a corner portion.
【0006】本発明は上記問題点を解決するものであ
り、2段発泡法においてエネルギーロスを減らし、効率
良く、縦、横及び高さ方向の寸法均一性に優れたポリオ
レフィン発泡体の製造方法を提供することを目的とす
る。The present invention solves the above-mentioned problems, and provides a method for producing a polyolefin foam having reduced energy loss in a two-stage foaming method, and having excellent dimensional uniformity in the vertical, horizontal and height directions. The purpose is to provide.
【0007】[0007]
【課題を解決するための手段】本発明のポリオレフィン
発泡体の製造方法は、ポリオレフィン、架橋剤及び発泡
剤からなる混和物を用いてポリオレフィン発泡体を製造
する方法において、上記混和物を一次金型に充填し、5
0kg/cm2 以上の加圧状態で加熱して架橋剤及び発
泡剤の一部を分解させ、その後、除圧することにより該
混和物を一次膨張させて一次発泡体を製造し、次いで、
該一次発泡体を最終発泡体製品の形状に対応する断面を
有する非密閉の閉鎖しうる二次型内に入れて加熱し、常
圧下で上記発泡剤の残部を分解させて二次発泡させ二次
発泡体を製造し、更に、該二次発泡体を最終発泡体製品
の形状に対応するとともに上記二次発泡体よりも小さい
断面を有する非密閉の閉鎖しうる冷却専用型内に入れ、
冷却下圧縮成形することを特徴とする。The method for producing a polyolefin foam of the present invention is a method for producing a polyolefin foam using an admixture comprising a polyolefin, a crosslinking agent and a foaming agent. And fill 5
By heating under a pressurized state of 0 kg / cm 2 or more to decompose a part of the crosslinking agent and the foaming agent, then, the pressure-reducing pressure causes the mixture to undergo primary expansion to produce a primary foam,
The primary foam is placed in a non-closeable, closable secondary mold having a cross section corresponding to the shape of the final foam product, heated, and the remaining foaming agent is decomposed under normal pressure to form a secondary foam. Producing a secondary foam, further placing the secondary foam in a non-closeable, closable, cooling-only mold corresponding to the shape of the final foam product and having a smaller cross-section than the secondary foam;
It is characterized by compression molding under cooling.
【0008】本発明において「ポリオレフィン」とは、
例えば、通常市販されている高圧法、中圧法又は低圧法
により製造されたポリエチレン、エチレン−プロピレン
共重合体、エチレン−ブテン共重合体、エチレン−酢酸
ビニル共重合体、エチレンとメチル、エチル、プロピル
若しくはブチルの各アクリル酸エステル(このエステル
の含有量;45モル%以内)との共重合体、又はこれら
のそれぞれ塩素含有率60重量%まで塩素化したもの、
更に、これら二種以上の混合物、又はこれらとアイソタ
クチックポリプロピレン若しくはアタクチックポリプロ
ピレンとの混合物等である。In the present invention, “polyolefin” refers to
For example, polyethylene, an ethylene-propylene copolymer, an ethylene-butene copolymer, an ethylene-vinyl acetate copolymer, ethylene and methyl, ethyl, propyl which are usually produced by a high pressure method, a medium pressure method or a low pressure method which are commercially available Or a copolymer of butyl with each acrylate (the content of this ester; within 45 mol%), or those chlorinated to a chlorine content of 60% by weight,
Further, a mixture of two or more of these, or a mixture of these with isotactic polypropylene or atactic polypropylene, and the like.
【0009】本発明にいう「架橋剤」とは、上記ポリオ
レフィン中において少なくともポリオレフィンの流動開
始温度以上の分解温度を有するものであって、加熱によ
り分解され、遊離ラジカルを発生してその分子間に架橋
結合を生じせしめるラジカル発生剤である有機過酸化物
等である。例えばジクミルパーオキサイド,2、5−ジ
メチル−2、5−ビス−ターシャリーブチルパーオキシ
ヘキサン,1、3−ビス−ターシャリーパーオキシ−イ
ソプロピルベンゼン等である。本発明にいう「発泡剤」
とは、上記ポリオレフィンの流動開始温度以上の分解温
度を有するもので、例えば、アゾジカルボンアミド、ジ
ニトロソペンタメチレンテトラミン等である。The term "crosslinking agent" as used in the present invention means a compound having a decomposition temperature at least equal to the flow starting temperature of the polyolefin in the above-mentioned polyolefin. Organic peroxides and the like, which are radical generators that cause cross-linking. For example, dicumyl peroxide, 2,5-dimethyl-2,5-bis-tert-butylperoxyhexane, 1,3-bis-tert-peroxy-isopropylbenzene, and the like. "Blowing agent" in the present invention
The term "having a decomposition temperature equal to or higher than the flow start temperature of the polyolefin" means, for example, azodicarbonamide, dinitrosopentamethylenetetramine and the like.
【0010】また、本発明において、発泡状態をコント
ロールするために、尿素を主成分とする化合物、酸化亜
鉛、酸化鉛等の金属酸化物、低級若しくは高級脂肪酸又
は低級若しくは高級脂肪酸の金属塩等の発泡助剤等を添
加することができる。更に、物性改善のためにカーボン
ブラック、亜鉛華、酸化チタン、その他常用の配合剤を
添加することもできる。In the present invention, in order to control the foaming state, compounds containing urea as a main component, metal oxides such as zinc oxide and lead oxide, lower or higher fatty acids or metal salts of lower or higher fatty acids, etc. A foaming aid and the like can be added. Further, carbon black, zinc white, titanium oxide, and other commonly used additives can be added to improve physical properties.
【0011】本発明では、「二次発泡体を最終発泡体製
品の形状に対応するとともに上記二次発泡体よりも小さ
い断面を有する非密閉の閉鎖しうる冷却専用型内に入
れ、冷却下圧縮成形すること」に特徴がある。このよう
に、別に設けた冷却専用型により冷却成形をするのは、
二次型の冷却、加熱の繰り返しをなくすことができエネ
ルギー効率を改善できると共に、冷却専用型は常時冷媒
により冷却しておくことが可能となり低温状態に維持さ
れるため、冷却時間も極めて短くすることができるから
である。[0011] In the present invention, "the secondary foam is placed in a non-closeable and closable dedicated cooling mold having a cross section smaller than that of the secondary foam and corresponding to the shape of the final foam product. Molding ". In this way, cooling molding using a separate cooling mold is
Repetition of cooling and heating of the secondary mold can be eliminated and energy efficiency can be improved.Also, the cooling-only type can always be cooled with a refrigerant and maintained at a low temperature, so the cooling time is also extremely short. Because you can do it.
【0012】上記「ポリオレフィン発泡体の形状に対応
する」とは、冷却専用型の内部空間形状が、このポリオ
レフィン発泡体の形状に略相似形状であることを意味す
る。また、二次発泡直後の二次発泡体の寸法は、所望の
最終製品の寸法より2〜10%大きいものとし、更に冷
却専用型の内部空間寸法を、上記発泡直後の発泡体寸法
より1〜8%小さいものとすることが好ましい。前者を
2〜10%と大きくするのは、発泡体の経時収縮を考慮
したものであり、収縮分を予め大きくしておき、収縮後
の寸法が所望の最終製品寸法を確保するようにするため
であり、後者を1〜8%と小さくするのは、発泡体を冷
却専用型に完全に密着させ成形精度をよくすると共に、
冷却効率を高めるためである。1%未満の場合は、型へ
の発泡体の密着が不充分となり上記効果が期待できず、
8%を超える場合は発泡体へ過剰の負荷がかかり逆に成
形精度の低下を招来する。また、上記冷却専用型は閉鎖
時に非密閉である。このようにすることにより、この型
において冷却下の圧縮成形時に空気溜りによる成形不良
の発生を防止できるからである。The expression "corresponding to the shape of the polyolefin foam" means that the internal space shape of the cooling-only type is substantially similar to the shape of the polyolefin foam. The size of the secondary foam immediately after the secondary foaming is 2 to 10% larger than the size of the desired final product. Preferably, it is 8% smaller. The reason for increasing the former to 2 to 10% is to take into account the temporal shrinkage of the foam, and to increase the amount of shrinkage in advance so that the dimensions after shrinkage can secure the desired final product dimensions. The reason why the latter is reduced to 1 to 8% is that the foam is completely adhered to the cooling-only mold to improve the molding accuracy,
This is to increase the cooling efficiency. If the amount is less than 1%, the adhesion of the foam to the mold is insufficient, and the above effects cannot be expected.
If it exceeds 8%, an excessive load is applied to the foam, and conversely, the molding accuracy is lowered. The cooling only type is not hermetically closed when closed. By doing so, it is possible to prevent molding defects due to air pockets during compression molding under cooling in this mold.
【0013】[0013]
【作用】従来、冷却した2板の平板に発泡体を挟み込
み、わずかに圧縮した状態で成形する場合は、平板によ
る圧縮により厚さ方向は均一になるものの、側方部に応
力がかかり、特にその中央部分を中心として脹らみが発
生してしまう。また、この場合は、発泡体が側面中央部
分へ引っぱられる如く歪をもった状態で圧縮成形されて
いるため、経時により発泡体の4隅部分にヒケが発生す
る。これに対し、本発明では、その冷却下の圧縮成形を
最終製品の形状に対応する断面を有する冷却専用型に入
れて行う。従って、成形体の厚さ方向はもちろん、その
縦、横方向も冷却専用型の側方部分により発泡体の膨張
が規制されるので、この型面によりその発泡体が圧縮成
形される際、発泡体側方中央部が膨らむことはなく、冷
却専用型の内部空間通りに均一な形状、寸法に冷却成形
される。Conventionally, when a foam is sandwiched between two cooled flat plates and molded in a slightly compressed state, although the thickness direction becomes uniform due to the compression by the flat plate, stress is applied to the lateral portions, Bulging occurs around the central portion. Further, in this case, since the foam is compression-molded in a state of being strained so as to be pulled toward the center portion of the side surface, sink occurs at the four corners of the foam over time. On the other hand, in the present invention, the compression molding under the cooling is performed in a cooling-only mold having a cross section corresponding to the shape of the final product. Therefore, the expansion of the foam is regulated not only in the thickness direction of the molded body, but also in the vertical and horizontal directions thereof, by the side portions of the cooling-only mold. The central part on the side of the body does not expand, and is cooled and formed into a uniform shape and dimensions according to the internal space of the cooling-only type.
【0014】更に、発泡体の表面を平滑化し且つ寸法精
度を良くするする方法としては、発泡完了後の二次型を
そのまま冷却し最終発泡体を冷却成形する方法(本発明
者が先に出願した特願平4−179152号)が考えら
れる。この方法は、極めて優れた冷却成形を人手を要す
ることなく短時間にできるという長所を有するものの、
同一型で加熱、冷却を繰り返すため、エネルギー効率が
十分とはいえない。これに対し、本発明では、二次型と
は別に冷却専用型を用いるので、二次型の冷却、加熱の
繰り返しをなくすことができ、そのためエネルギー効率
を改善できると共に、冷却専用型は常時冷媒により冷却
しておくことが可能となり、低温状態に維持されるた
め、冷却時間も極めて短くすることもできる。Further, as a method for smoothing the surface of the foam and improving the dimensional accuracy, a method of cooling the secondary mold after completion of foaming as it is and cooling and molding the final foam (the inventor of the present invention previously filed the application) Japanese Patent Application No. 4-179152) is conceivable. Although this method has the advantage that extremely excellent cooling molding can be performed in a short time without requiring any manual operation,
Since heating and cooling are repeated with the same mold, energy efficiency is not sufficient. On the other hand, in the present invention, since the cooling only type is used separately from the secondary type, it is possible to eliminate the repetition of cooling and heating of the secondary type, so that the energy efficiency can be improved. The cooling time can be kept low, and the cooling time can be extremely shortened.
【0015】[0015]
【実施例】以下、実施例により本発明を具体的に説明す
る。 実施例1 メルトインデックス1.0のポリエチレン100重量部
(以下、部という。)に、アゾジカルボンアミド5部、
ジクミルパーオキサイド2部及び酸化亜鉛0.5部から
なる組成物を表面温度100℃のロール上で混練して混
和物を得た。この混和物6.8kgを一次金型(420
mm×420mm×42mm)に充填し、70kg/c
m2 の加圧下で、且つ160℃で30分間加熱した後、
高温熱時に除圧し10倍程度に発泡膨張した一次発泡体
(880mm×880mm×86mm)を得た。この高
温状態の一次発泡体を、二次型(内部空間寸法:100
0mm×1000mm×100mm)に入れ、型上面及
び下面を構成する金属板の熱媒流路にスチームを導通さ
せることによりその金属板を165℃に維持し、この一
次発泡体を30分加熱して、二次発泡をさせて二次発泡
体を得た。The present invention will be described below in detail with reference to examples. Example 1 To 100 parts by weight of polyethylene having a melt index of 1.0 (hereinafter, referred to as parts), 5 parts of azodicarbonamide,
A composition comprising 2 parts of dicumyl peroxide and 0.5 part of zinc oxide was kneaded on a roll having a surface temperature of 100 ° C. to obtain an admixture. 6.8 kg of this mixture is placed in a primary mold (420
mm × 420mm × 42mm), 70kg / c
After heating at 160 ° C. for 30 minutes under pressure of m 2 ,
The primary foam (880 mm x 880 mm x 86 mm) was decompressed at the time of high temperature heat and foamed and expanded about 10 times. This primary foam in a high temperature state is placed in a secondary mold (inner space size: 100
0 mm × 1000 mm × 100 mm), and the steam is conducted through the heat medium flow paths of the metal plates constituting the upper and lower surfaces of the mold to maintain the metal plate at 165 ° C. and heat the primary foam for 30 minutes. And secondary foaming to obtain a secondary foam.
【0016】この二次発泡体を二次型より取り出し、そ
の寸法を測ったところ、1030mm×1030mm×
103mmであった。この高温状態の二次発泡体を、冷
却水により20℃に冷却されている冷却専用型(100
0mm×1000mm×100mm)内に入れ20分間
冷却をして圧縮成形を行い、最終発泡体を得た。この最
終発泡体を1週間経時させ、縦、横、高さ方向の寸法を
調査したところ、表面が平滑であると共に、縦、横が9
80〜985mm、高さが98〜95mmと極めて均一
な成形状態の発泡体が得られた。The secondary foam was taken out of the secondary mold and its dimensions were measured. The dimensions were 1030 mm × 1030 mm ×
103 mm. The secondary foam in the high temperature state is cooled to a temperature of 20 ° C. by cooling water (100 cooling only type).
(0 mm × 1000 mm × 100 mm) and cooled for 20 minutes to perform compression molding to obtain a final foam. The final foam was aged for one week, and the length, width and height dimensions were examined. The surface was smooth and the height and width were 9
An extremely uniform foam of 80 to 985 mm and a height of 98 to 95 mm was obtained.
【0017】比較例1 実施例1と同様の方法により得た一次発泡体を、図1に
示すような一対の加熱板2で挟まれた冷却成形用型1
(内部空間寸法:1000mm×1000mm×100
mm)に入れ、熱媒流路21にスチームを導通させるこ
とにより165℃に維持された加熱板2を用いて、この
冷却成形用型を介して30分間加熱した。加熱完了後、
加熱板2に供給していたスチームを止め、同時に冷却成
形用型1の冷媒流路111、121に常温の冷却水を流
通させた。Comparative Example 1 A primary molding obtained by the same method as in Example 1 was cooled and pressed by a pair of heating plates 2 as shown in FIG.
(Internal space dimensions: 1000 mm x 1000 mm x 100
mm), and heating was performed for 30 minutes through the cooling mold using the heating plate 2 maintained at 165 ° C. by passing steam through the heat medium flow path 21. After heating is complete,
The steam supplied to the heating plate 2 was stopped, and at the same time, normal-temperature cooling water was allowed to flow through the coolant channels 111 and 121 of the cooling mold 1.
【0018】その結果、冷却成形用型1の側方型枠11
部分は約3分後に50℃前後まで降温し、発泡体側方外
周部は約30分後に90℃まで降温した。この時点で、
最終発泡体を取り出すと同時に冷却水を止め、再び加熱
板2へスチームを流通させた。これにより加熱板2が再
び165℃となるのに約18分要した。従って、冷却開
始→冷却完了→冷却成形用型の再昇温に要した時間は4
8分であり、実施例1と比較すると約2.5倍の時間を
要した。尚、得られた最終発泡体を1週間経時させた
後、縦、横、高さの寸法を調査したところ、縦、横が9
83〜988mm、高さが96〜99mmであり、本例
においても実施例1と同様に、極めて均一な成形状態の
発泡体が得られた。As a result, the side frame 11 of the cooling mold 1 is formed.
The temperature of the portion was lowered to about 50 ° C. after about 3 minutes, and the temperature of the outer peripheral portion of the foam was lowered to 90 ° C. after about 30 minutes. at this point,
The cooling water was stopped at the same time when the final foam was taken out, and steam was allowed to flow again to the heating plate 2. Thus, it took about 18 minutes for the heating plate 2 to reach 165 ° C. again. Therefore, the time required for starting the cooling → the completion of the cooling → the reheating of the cooling mold is 4 hours.
8 minutes, about 2.5 times as long as that of Example 1. After the obtained final foam was aged for one week, the length, width, and height were examined.
The foam was 83 to 988 mm and the height was 96 to 99 mm. In this example, as in Example 1, an extremely uniform foam was obtained.
【0019】比較例2 実施例1と同様の方法により得た二次発泡体を2板の平
板に挟み込み、20分間冷却成形を行った。その結果、
得られた発泡体を1週間経時させた後寸法を測ったとこ
ろ、縦、横寸法が992〜970mm、高さ寸法が92
〜98mmであり、特に縦、横方向の寸法バラツキが大
きかった。Comparative Example 2 The secondary foam obtained in the same manner as in Example 1 was sandwiched between two flat plates and subjected to cooling molding for 20 minutes. as a result,
After the obtained foam was aged for one week, the dimensions were measured. The vertical and horizontal dimensions were 992 to 970 mm, and the height dimension was 92.
9898 mm, and the dimensional variation in the vertical and horizontal directions was particularly large.
【0020】尚、本発明においては、上記具体的実施例
に示すものに限られず、目的、用途に応じて本発明の範
囲内で種々変更した実施例とすることができる。即ち、
上記実施例では、1つの発泡体を圧縮成形するための冷
却成形用型又は冷却専用型を用いたが、これに限らず、
例えば、複数の発泡体を同時に冷却又は圧縮成形できる
ように、側方型枠と平板を順次積層したような積層型の
各冷却型としてもよい。また、これらの冷却型には冷媒
を流すことができる冷媒流路を持ち、この流路に冷媒を
流して冷却してもよい。この冷媒流路の断面、大きさ、
数も特に限定されないし、その流入口及び出口の数も種
々選択される。また、上記冷却型の内部空間形状は、四
角板状(若しくは直方体状)のみならず、目的とする製
品形状に応じた種々の形状とすることができる。更に、
加熱発泡における架橋剤及び発泡剤は、略完全に分解さ
せるのが好ましいが、これに限らず、未分解のものが残
存していてもよい。It should be noted that the present invention is not limited to the specific embodiments described above, but can be variously modified within the scope of the present invention in accordance with the purpose and application. That is,
In the above embodiment, a cooling mold or a cooling-only mold for compression-molding one foam was used.
For example, each of the cooling molds may be a lamination type in which side molds and flat plates are sequentially laminated so that a plurality of foams can be simultaneously cooled or compression molded. In addition, these cooling types may have a coolant channel through which a coolant can flow, and the coolant may be caused to flow through this channel to perform cooling. The cross-section, size,
The number is not particularly limited, and the number of inlets and outlets is also variously selected. The shape of the internal space of the cooling mold can be not only a square plate (or a rectangular parallelepiped), but also various shapes according to the desired product shape. Furthermore,
It is preferable that the cross-linking agent and the foaming agent in the heat foaming are decomposed almost completely, but the present invention is not limited to this, and undecomposed materials may remain.
【0021】[0021]
【発明の効果】本発明の製造方法によれば、上記作用に
示すように、2段発泡法においてエネルギーロスを減ら
し、効率良く、表面が平滑で、且つ縦、横及び高さ方向
の寸法均一性に優れる最終発泡体を製造できる。According to the manufacturing method of the present invention, as described above, the energy loss can be reduced in the two-stage foaming method, the surface can be efficiently smoothed, and the dimensional uniformity in the vertical, horizontal and height directions can be achieved. A final foam having excellent properties can be produced.
【図1】比較例1で用いたポリオレフィン発泡体の製造
装置の発泡成形部を示す説明断面図である。FIG. 1 is an explanatory sectional view showing a foam molding section of an apparatus for producing a polyolefin foam used in Comparative Example 1.
1;冷却成形用型、11;側方型枠、11a;上型枠、
11b;下型枠、111;冷媒流路、12a、12b;
平板、121;冷媒流路、1211;管状体、122;
中板、123;板状体、2;加熱板、21;熱媒流路、
22;金属製箱状体、23;底板、24;管状体、2
5;リブ、3;内部空間、4;ボルト、5;ボルト、
6;二次型。1; mold for cooling molding; 11; side mold; 11a; upper mold;
11b; lower mold, 111; refrigerant flow path, 12a, 12b;
Flat plate, 121; refrigerant channel, 1211; tubular body, 122;
Medium plate, 123; plate, 2; heating plate, 21;
22; metal box, 23; bottom plate, 24; tubular, 2
5; rib, 3; internal space, 4; bolt, 5; bolt,
6; secondary type.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI B29K 105:04 105:24 C08L 23:00 (58)調査した分野(Int.Cl.6,DB名) B29C 39/00 - 39/44 B29C 67/20 C08J 9/06 B29C 35/16 ──────────────────────────────────────────────────の Continued on the front page (51) Int.Cl. 6 identification symbol FI B29K 105: 04 105: 24 C08L 23:00 (58) Fields surveyed (Int.Cl. 6 , DB name) B29C 39/00- 39/44 B29C 67/20 C08J 9/06 B29C 35/16
Claims (1)
なる混和物を用いてポリオレフィン発泡体を製造する方
法において、 上記混和物を一次金型に充填し、50kg/cm2 以上
の加圧状態で加熱して架橋剤及び発泡剤の一部を分解さ
せ、その後、除圧することにより該混和物を一次膨張さ
せて一次発泡体を製造し、 次いで、該一次発泡体を最終発泡体製品の形状に対応す
る断面を有する非密閉の閉鎖しうる二次型内に入れて加
熱し、常圧下で上記発泡剤の残部を分解させて二次発泡
させ二次発泡体を製造し、 更に、該二次発泡体を最終発泡体製品の形状に対応する
とともに上記二次発泡体よりも小さい断面を有する非密
閉の閉鎖しうる冷却専用型内に入れ、冷却下圧縮成形す
ることを特徴とするポリオレフィン発泡体の製造方法。1. A method for producing a polyolefin foam using an admixture of a polyolefin, a cross-linking agent and a foaming agent, wherein the admixture is filled in a primary mold and heated under a pressure of 50 kg / cm 2 or more. To partially decompose the cross-linking agent and the foaming agent, and then to firstly expand the mixture by depressurizing to produce a primary foam. Then, the primary foam corresponds to the shape of the final foam product. Into a non-closed closable secondary mold having a cross-section to be heated and heated to decompose the remainder of the foaming agent under normal pressure to produce secondary foam, thereby producing a secondary foam. The polyolefin foam is characterized in that the body is placed in a non-closed, closable and exclusive cooling mold having a cross section smaller than that of the secondary foam and corresponding to the shape of the final foam product, and compression-molded under cooling. Production method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4351625A JP2869475B2 (en) | 1992-12-08 | 1992-12-08 | Method for producing polyolefin foam |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4351625A JP2869475B2 (en) | 1992-12-08 | 1992-12-08 | Method for producing polyolefin foam |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH06170866A JPH06170866A (en) | 1994-06-21 |
| JP2869475B2 true JP2869475B2 (en) | 1999-03-10 |
Family
ID=18418532
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4351625A Expired - Lifetime JP2869475B2 (en) | 1992-12-08 | 1992-12-08 | Method for producing polyolefin foam |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2869475B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012236911A (en) * | 2011-05-11 | 2012-12-06 | Inoac Corp | Method for producing foam body |
-
1992
- 1992-12-08 JP JP4351625A patent/JP2869475B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH06170866A (en) | 1994-06-21 |
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