JPH02258327A - Manufacture of olefin resin foam molded material - Google Patents
Manufacture of olefin resin foam molded materialInfo
- Publication number
- JPH02258327A JPH02258327A JP1082465A JP8246589A JPH02258327A JP H02258327 A JPH02258327 A JP H02258327A JP 1082465 A JP1082465 A JP 1082465A JP 8246589 A JP8246589 A JP 8246589A JP H02258327 A JPH02258327 A JP H02258327A
- Authority
- JP
- Japan
- Prior art keywords
- mold
- molded product
- fixed side
- molded
- valve
- 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
Links
- 229920005672 polyolefin resin Polymers 0.000 title claims description 25
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 239000006260 foam Substances 0.000 title claims description 11
- 239000000463 material Substances 0.000 title description 2
- 238000001816 cooling Methods 0.000 claims abstract description 22
- 239000002245 particle Substances 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 15
- 238000005187 foaming Methods 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
- 238000004904 shortening Methods 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 2
- 238000005336 cracking Methods 0.000 abstract description 10
- 238000000465 moulding Methods 0.000 abstract description 6
- 238000001125 extrusion Methods 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000004604 Blowing Agent Substances 0.000 description 6
- 239000000498 cooling water Substances 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- -1 polypropylene Polymers 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000002270 dispersing agent Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 238000010097 foam moulding Methods 0.000 description 3
- 229910001872 inorganic gas Inorganic materials 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000011162 core material Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 229920005674 ethylene-propylene random copolymer Polymers 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- NBVXSUQYWXRMNV-UHFFFAOYSA-N monofluoromethane Natural products FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 2
- 229920001083 polybutene Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- BOSAWIQFTJIYIS-UHFFFAOYSA-N 1,1,1-trichloro-2,2,2-trifluoroethane Chemical compound FC(F)(F)C(Cl)(Cl)Cl BOSAWIQFTJIYIS-UHFFFAOYSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 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
- 239000004698 Polyethylene Substances 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 229920005676 ethylene-propylene block copolymer Polymers 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 229940073584 methylene chloride Drugs 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- UOURRHZRLGCVDA-UHFFFAOYSA-D pentazinc;dicarbonate;hexahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Zn+2].[Zn+2].[Zn+2].[Zn+2].[Zn+2].[O-]C([O-])=O.[O-]C([O-])=O UOURRHZRLGCVDA-UHFFFAOYSA-D 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 229920001384 propylene homopolymer Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
Landscapes
- Moulds For Moulding Plastics Or The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はオレフィン系樹脂発泡成形体の製造方法に関し
、更に詳しくは、発泡成形体の金型からの離型を容易に
して従来よりも高い面圧で離型することにより、冷却時
間の大巾な短縮を実現したオレフィン系樹脂発泡成形体
の製造方法に関する。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a method for producing an olefin resin foam molded product, and more specifically, the present invention relates to a method for producing an olefin resin foam molded product. The present invention relates to a method for producing an olefin resin foam molded product that achieves a significant reduction in cooling time by releasing from the mold using surface pressure.
ポリプロピレン、ポリエチレン等オレフィン系樹脂の発
泡成形体(以下、成形体と記す)は自動車用バンパー芯
材等のエネルギー吸収体や、緩i1j包装材、通雨等に
広く利用されている。Foamed molded products of olefin resins such as polypropylene and polyethylene (hereinafter referred to as molded products) are widely used as energy absorbers such as automobile bumper core materials, loose I1J packaging materials, rain ventilation, and the like.
オレフィン系樹脂の成形体は予備発泡粒子を第1図に示
す如き金型内に充填し、蒸気等により加熱して膨張融着
させた後、水等により冷却して、成形体をエゼクトビン
により固定側金型より外に突き出させて離型するという
方法が一般的である。For molded bodies of olefin resin, pre-expanded particles are filled into a mold as shown in Figure 1, heated with steam etc. to expand and fuse, cooled with water etc., and fixed in an eject bin. A common method is to release the mold by protruding it from the side mold.
ところで、上記方法において冷却時間を決定する要因は
成形体の発泡圧力(通称面圧)であって、−M的には最
高約0.4 kg/c4Gである。この面圧より高い状
態で離型すると、成形体室(16)内の成形体と固定側
中型(12)の間の摺動抵抗が大きく、エゼクトビン(
9)による離型押出圧力が通常より大きくなるために、
無理をして離型押出すると第2図(A)、(B)に示す
如く、成形体(31)はエゼクトピン(9)の弾性限界
を趨える圧縮応力(離型押出圧力に等しい)のために成
形体と接触しているエゼクトピン(9)のピン頭部(9
a)の円周部分に円環状の割れ(32)(通称ピン割れ
)が発生する。この場合における成形体の圧縮応力は、
一般にカタログ等で公表されているデータよりも常に低
い、この理由は、成形体内部の温度は常温よりかなり高
温で、約60〜80°Cである。成形体の表面温度は常
温付近であるが、成形体は発泡体であるため断熱効果が
あり、内部塩冷却して常温になるまでにかなりの時間を
要するので、内部は外部温度に比較して高温となってい
るので圧縮強度は低い。By the way, in the above method, the factor that determines the cooling time is the foaming pressure (commonly called surface pressure) of the molded article, which is a maximum of about 0.4 kg/c4G in terms of -M. If the mold is released in a state higher than this surface pressure, the sliding resistance between the molded body in the molded body chamber (16) and the stationary side middle mold (12) will be large, and the eject bin (
9) Because the mold release extrusion pressure becomes higher than usual,
If the mold release extrusion is forced, as shown in FIGS. 2(A) and (B), the molded body (31) will be damaged due to compressive stress (equal to the mold release extrusion pressure) exceeding the elastic limit of the eject pin (9). The pin head (9) of the eject pin (9) that is in contact with the molded body is
An annular crack (32) (commonly known as a pin crack) occurs in the circumferential portion of a). The compressive stress of the compact in this case is
The reason for this is that the temperature inside the molded body is much higher than normal temperature, which is about 60 to 80°C, which is generally lower than the data published in catalogs and the like. The surface temperature of the molded product is around room temperature, but since the molded product is a foam, it has an insulating effect, and it takes a considerable amount of time for the inside to cool down to room temperature, so the inside temperature is lower than the outside temperature. Since the temperature is high, the compressive strength is low.
ところで、成形体の圧縮強度は材質及び発泡倍率により
異なるが、室温以上では一般に温度と反比例の関係にな
っている。従って、冷却時間を短縮した状態でエゼクト
ピン(9)を使用して離型押出しすると上記ピン割れが
避けられない、このピン割れを避けるために、離型押出
し時に固定側蒸気室(17)にエゼクト用圧縮空気を送
り込み、固定側中型(12)より離型押出し作用を行わ
せることが常用されるが、この方法も顕著な効果を示さ
ない。Incidentally, the compressive strength of a molded article varies depending on the material and the expansion ratio, but is generally inversely proportional to the temperature above room temperature. Therefore, if the eject pin (9) is used for mold release extrusion with the cooling time shortened, the above-mentioned pin cracking is unavoidable.In order to avoid this pin cracking, the eject pin (17) is It is commonly used to send in compressed air to perform a mold release extrusion action from the fixed middle mold (12), but this method also does not have a significant effect.
この理由は、上記のエゼクト用圧縮空気は成形体室(1
6)の成形体を固定側中型(12)から離型押出し作用
を行う前に、第1図に示される固定側蒸気室(17)側
の固定側中型(12)の立上り部と相対する成形体の間
隙(a)から移動側中型(13)を経由して移動側蒸気
室(18)にシッートパスするために、固定側蒸気室(
17)側の空気圧力が十分に上昇せず、その結果、離型
押出し効果が有効に発渾されない、またエゼクト用圧縮
空気のシッートパスが少なくて離型押出し効果があるの
も見られるが、通常、成形体室(16)は1個以上の複
数であることが多く、この場合は早(離型押出しされた
成形体室(16)からエゼクト用圧縮空気が吹き出され
てしまい、他の成形体室(16)に残留している成形体
にはエゼクト州離型押出し効果が発渾されず、結果とし
て前記ビン割れが避けられず、不良品の原因になる。The reason for this is that the above compressed air for ejecting is
Before extruding the molded product in step 6 from the stationary side middle mold (12), the molded body is molded opposite to the rising part of the stationary side middle mold (12) on the side of the fixed side steam chamber (17) shown in Fig. 1. In order to make a seat pass from the body gap (a) to the moving side steam chamber (18) via the moving side medium mold (13), the fixed side steam chamber (
17) The air pressure on the side does not rise sufficiently, and as a result, the mold release extrusion effect is not developed effectively.Also, the sheet pass of the compressed air for eject is small, and the mold release extrusion effect is observed. In many cases, there are one or more molded body chambers (16), and in this case, compressed air for ejecting may be blown out from the molded body chamber (16) after mold release extrusion, causing damage to other molded bodies. The molded body remaining in the chamber (16) does not undergo the extrusion effect during extrusion, and as a result, the bottle cracking is unavoidable, resulting in defective products.
上述の如く、従来のポリオレフィンの型内発泡成形法で
は、常用の冷却時間を短縮して離型押出しを行うとビン
割れが発生するので、冷却時間を短縮することは不可能
である。As mentioned above, in the conventional in-mold foam molding method for polyolefin, bottle cracking occurs when mold release extrusion is performed with a shortened cooling time, so it is impossible to shorten the cooling time.
本発明者等は、かかる実情に鑑み鋭意研究の結果、通常
の離型取出し前に成形体を移動側金型に吸引移動させて
成形体の固定側接触面を一旦大気圧雰囲気に1部又は全
部を開放した後、再度型締めし又はそのまま直ちに型開
き離型することにより、離型を容易とし、その結果、従
来より高い面圧での離型が可能となり、冷却時間を大巾
に短縮でき、成形サイクルの大巾な短縮が可能となるこ
とを見出し、本発明を完成した。In view of the above circumstances, the inventors of the present invention have conducted extensive research, and have determined that the fixed side contact surface of the molded body is partially exposed to atmospheric pressure by suctioning and moving the molded body to the movable mold before the normal removal from the mold. After opening everything, the mold can be re-clamped or the mold can be opened and released immediately, making it easier to release the mold.As a result, it is possible to release the mold with a higher surface pressure than before, greatly shortening the cooling time. The present invention was completed based on the discovery that it is possible to significantly shorten the molding cycle.
即ち、本発明の第1は、オレフィン系樹脂粒子から発泡
成形体を製造するに際し、成形体を離型取出しする前に
移動側金型を真空減圧にして成形体を移動側金型に吸引
密着させながら型開きした後に型閉めを行い、移動側金
型を大気圧にすると共に成形体を固定側金型に移した後
、離型取出しすることにより冷却時間を短縮することを
特徴とするオレフィン系樹脂発泡体の製造方法を、本発
明の第2は、オレフィン系樹脂粒子から発泡成形体を製
造するに際し、成形体を離型取出しする前に移動側金型
を真空減圧にして成形体を吸引密着させながら成形体が
固定側金型に残留できる位置まで型開きした後、移動側
金型を大気圧にすることにより冷却時間を短縮すること
を特徴とするオレフィン系樹脂発泡成形体の製造方法を
それぞれ内容とするものである。That is, the first aspect of the present invention is that when producing a foamed molded article from olefin resin particles, before removing the molded article from the mold, the movable mold is vacuumed and the molded article is suctioned and brought into close contact with the movable mold. The olefin is characterized in that the cooling time is shortened by opening the mold while moving the mold, closing the mold, bringing the movable mold to atmospheric pressure, transferring the molded product to the stationary mold, and then removing it from the mold. The second aspect of the present invention is a method for producing a foamed resin foam, in which when producing a foamed molded product from olefin resin particles, the movable mold is vacuum depressurized before the molded product is released from the mold. Manufacture of an olefin resin foam molded article characterized by shortening the cooling time by bringing the movable mold to atmospheric pressure after opening the mold to a position where the molded article can remain in the stationary mold while being brought into close contact with suction. The contents of each method are as follows.
本発明に用いられるオレフィン系樹脂としては、例えば
プロピレンホモポリマー、エチレン−プロピレンランダ
ムコポリマー、エチレンープロピレンブロックコポリマ
ー、エチレン−プロピレン−ブテンランダムターポリマ
ー、プロピレン−塩化ビニルコポリマー、プロピレン−
ブテンコポリマ、プロピレン−無水マレイン酸コポリマ
ー等が挙げられるが、これらの中では立体規則性重合方
法によって製造されたエチレン−プロピレンコポリマー
が好ましい、これらは単独で用いてもよく、2種以上混
合使用してもよい。Examples of the olefin resin used in the present invention include propylene homopolymer, ethylene-propylene random copolymer, ethylene-propylene block copolymer, ethylene-propylene-butene random terpolymer, propylene-vinyl chloride copolymer, and propylene-vinyl chloride copolymer.
Examples include butene copolymers, propylene-maleic anhydride copolymers, etc., but among these, ethylene-propylene copolymers produced by stereoregular polymerization are preferred; these may be used alone or in combination of two or more. Good too.
これらのオレフィン系樹脂は無架橋の状態が好ましいが
、パーオキサイドや放射線等により架橋させて用いても
よい、またオレフィン系樹脂と混合使用可能な他の熱可
塑性樹脂、例えば低密度ポリエチレン、直鎖低密度ポリ
エチレン、ポリスチレン、ポリブテン、アイオノマー等
をポリプロピレン系樹脂の性質が損なわれない範囲で混
合使用してもよい0例えば低密度ポリエチレン、直鎖低
密度ポリエチレン、ポリブテン、アイオノマーを併用す
る場合には、プロピレン系樹脂100部(重量部、以下
同じ)に対して5〜20部、ポリスチレンを併用する場
合には5〜1’O部が好ましい。These olefin resins are preferably in a non-crosslinked state, but they may be crosslinked with peroxide or radiation, or other thermoplastic resins that can be mixed with the olefin resins, such as low-density polyethylene, linear Low density polyethylene, polystyrene, polybutene, ionomer, etc. may be mixed and used as long as the properties of the polypropylene resin are not impaired.For example, when low density polyethylene, linear low density polyethylene, polybutene, ionomer, etc. are used together, It is preferably 5 to 20 parts per 100 parts (by weight, same hereinafter) of the propylene resin, and preferably 5 to 1'0 parts when polystyrene is used in combination.
これらのオレフィン系樹脂は、通常、予備発泡に利用さ
れ易いように予め押出機、ニーグー、バンバリーミキサ
−、ロール等を用いて溶融し、円柱状、楕円柱状、球状
、立方体状、直方体状等のような所望の粒子形状で、そ
の粒子の平均粒径が0.1−10閣、好ましくは0.7
〜5mになるように成形加工される。These olefin resins are usually melted in advance using an extruder, Nigoo mixer, Banbury mixer, roll, etc. so that they can be easily used for pre-foaming, and are shaped into cylinders, elliptical cylinders, spheres, cubes, rectangular parallelepipeds, etc. The desired particle shape is such that the average particle size of the particles is 0.1-10 mm, preferably 0.7 mm.
It is molded to a length of ~5m.
予備発泡方法としては特に限定はないが、例えば、耐圧
容器中でオレフィン系樹脂粒子に揮発性発泡剤を含有さ
せ、撹拌しながら水中に分散させ、加圧下で所定の発泡
温度まで加熱した後、該水分散物を2〜10−φの開孔
オリフィスを通して低圧域に放出する方法等が利用され
る。There are no particular limitations on the pre-foaming method, but for example, olefin resin particles are made to contain a volatile blowing agent in a pressure-resistant container, dispersed in water with stirring, heated to a predetermined foaming temperature under pressure, and then A method is used in which the aqueous dispersion is discharged into a low pressure region through an orifice with a diameter of 2 to 10 mm.
本発明に使用されるオレフィン系樹脂粒子に含有させる
揮発性発泡剤としては、例えばプロパン、ブタン、ペン
タン、ヘキサン等の脂肪族炭化水素類;シクロペンタン
、シクロブタン等の脂環式炭化水素類;トリクロロモノ
フルオロメタン、ジクロロジフルオロメタン、ジクロロ
テトラフルオロエタン、トリクロロトリフルオロエタン
、メチルクロライド、メチレンクロライド、エチルクロ
ライド等のハロゲン化炭化水素類等が挙げられる。Volatile blowing agents to be contained in the olefin resin particles used in the present invention include, for example, aliphatic hydrocarbons such as propane, butane, pentane, and hexane; alicyclic hydrocarbons such as cyclopentane and cyclobutane; Examples include halogenated hydrocarbons such as monofluoromethane, dichlorodifluoromethane, dichlorotetrafluoroethane, trichlorotrifluoroethane, methyl chloride, methylene chloride, and ethyl chloride.
これらの発泡剤は単独で用いてもよく、2種以上併用し
てもよい、また、その使用量にも特に限定はなく、所望
のオレフィン系樹脂予備発泡粒子の発泡度に応じて適宜
使用すればよく、通常その使用量はオレフィン系樹脂1
00部に対して5〜50部である。These blowing agents may be used alone or in combination of two or more, and the amount used is not particularly limited, and may be used as appropriate depending on the degree of foaming of the desired pre-expanded olefin resin particles. Usually, the amount used is olefin resin 1
00 parts to 5 to 50 parts.
前記水分散物の調製に際しては、分散剤として、例えば
第3リン酸カルシウム、塩基性炭酸マグネシウム、塩基
性炭酸亜鉛、炭酸カルシウム等や、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、n−パラフ
ィンスルホン酸ソーダ、α−オレフィンスルホン酸ソー
ダ等が使用され得る。When preparing the aqueous dispersion, dispersants such as tertiary calcium phosphate, basic magnesium carbonate, basic zinc carbonate, calcium carbonate, etc., and a small amount of surfactant,
For example, sodium dodecylbenzenesulfonate, sodium n-paraffinsulfonate, sodium α-olefinsulfonate, etc. may be used.
かかる分散剤や界面活性剤の使用量は、その種類や用い
るオレフィン系樹脂粒子の種類とその使用量等によって
異なるが、通常、水100部に対して分散剤の場合で0
.2〜3部、界面活性剤の場合で0.001−0.1部
である。The amount of the dispersant or surfactant used varies depending on the type of the dispersant or surfactant, the type of olefin resin particles used, the amount used, etc., but usually 0 parts of the dispersant per 100 parts of water.
.. 2-3 parts, 0.001-0.1 part in case of surfactants.
また、前記揮発性発泡剤を含有したオレフィン系樹脂粒
子は水中での分散性を良好なものとするために、通常、
水100部に対して20〜100部添加されるのが好ま
しい。In addition, in order to improve the dispersibility of the olefin resin particles containing the volatile blowing agent in water, usually,
It is preferable to add 20 to 100 parts per 100 parts of water.
本発明は、オレフィン系樹脂の予備発泡粒子を用いた下
記の型内発泡成形法のいずれにも好適に適用される。The present invention is suitably applied to any of the following in-mold foam molding methods using pre-expanded particles of olefin resin.
(イ)オレフィン系樹脂の予備発泡粒子を無機ガスで加
圧処理して該粒子に無機ガスを含浸させた後に除圧し、
該粒子の内圧が1.18気圧以上である間に閉鎖し得る
が密閉し得ない金型に充填し、蒸気等で加熱融着し、型
通りの成形体とする方法(特公昭51−22951号公
報)、
(ロ)閉鎖し得るが密閉し得ない金型にオレフィン系樹
脂の予備発泡粒子を充填し、蒸気等で加熱融着した後、
金型から取出し、その体積が金型の容積の70〜110
%である間に加熱養生して型通りの成形体を製造する方
法(特開昭60−166442号公報)、
(ハ)金型と予備発泡粒子用容器(加圧充填容器)を均
一に加圧された状態にし、予備発泡粒子を無機ガスで圧
縮充填する方法(特開昭62−179927号公報)が
知られている。(a) pre-expanded particles of olefin resin are pressurized with an inorganic gas to impregnate the particles with the inorganic gas, and then the pressure is removed;
A method of filling the particles into a mold that can be closed but cannot be sealed while the internal pressure is 1.18 atm or more, and heating and fusing them with steam etc. to form a molded product according to the mold (Japanese Patent Publication No. 51-22951) (B) Fill a mold that can be closed but cannot be sealed with pre-expanded particles of olefin resin, and after heating and fusing them with steam, etc.
When taken out from the mold, its volume is 70 to 110 of the volume of the mold.
% (Japanese Unexamined Patent Publication No. 60-166442), (c) uniformly applying a mold and a container for pre-expanded particles (pressure filling container); A method (Japanese Unexamined Patent Publication No. 179927/1983) is known in which the particles are brought into a compressed state and the pre-expanded particles are compressed and filled with an inorganic gas.
尚、スチレン系樹脂に揮発性発泡剤を含有させたスチレ
ン系発泡樹脂に本発明を適用しても所期の効果が少ない
、即ち、スチレン系発泡樹脂の発泡成形において、通常
の冷却時間を短縮して離型する場合は、取出後に肉厚部
に部分的な三次発泡により膨らみが生じて正常な成形品
を得ることが出来ないからである。It should be noted that even if the present invention is applied to styrene-based foamed resin containing a volatile foaming agent, the desired effect will be small; that is, the usual cooling time will not be shortened in foam molding of styrene-based foamed resin. This is because if the mold is released by removing the mold, bulges will occur in the thick wall portion due to partial tertiary foaming after the mold is removed, making it impossible to obtain a normal molded product.
次に、前記予備発泡粒子から発泡体を製造する際に用い
られる本発明の製造装置の一例を示す図面に基づいて説
明する。Next, an explanation will be given based on drawings showing an example of the manufacturing apparatus of the present invention used when manufacturing a foam from the pre-expanded particles.
第3図は、本発明に用いられる製造装置を示す概要図で
、本発明の製造装置は、主として金型及び金型部品と真
空装置から構成されている。予備発泡粒子(1)は送粒
装置(図示せず)によりホッパー(2)に送粒貯蔵され
る。予備発泡粒子(1)を成形体室(16)内に充填す
る工程では固定側フレーム(10)と移動側フレーム(
11)が接触しているパーティングライン(p)を若干
(約2〜lO閤)開(と共に固定側ドレン弁(28)と
移動側ドレン弁(29)を開き、この状態で、シャッタ
ー(3)を開き、フィーダー(6)を開いて、充填用空
気弁(8)を開くことにより充填操作が行われる。充填
工程が終了するとフィーダー(6)がフィーダー開閉弁
(7)によって閉められ、次にシャッター(3)がシャ
ッター開閉弁(4)によって閉められる0次に、型閉め
が型開閉装置によって行われる。型開閉装置は図示しな
いが、通常の場合は金型を取付けているグイプレートと
油圧シリンダーで構成されており、油圧シリンダーの移
動によりグイプレートが移動して、金型の開閉が行われ
るようになっている。FIG. 3 is a schematic diagram showing a manufacturing apparatus used in the present invention, and the manufacturing apparatus of the present invention is mainly composed of a mold, mold parts, and a vacuum device. The pre-expanded particles (1) are fed and stored in a hopper (2) by a feeding device (not shown). In the step of filling the pre-expanded particles (1) into the molded body chamber (16), the fixed side frame (10) and the movable side frame (
Open the parting line (p) that the shutter (11) is in contact with slightly (approximately 2 to 10 liters) (and open the fixed side drain valve (28) and the movable side drain valve (29), and in this state, open the parting line (p) that the shutter (3 ), open the feeder (6), and open the filling air valve (8).When the filling process is finished, the feeder (6) is closed by the feeder on/off valve (7), and the next Next, the shutter (3) is closed by the shutter opening/closing valve (4).Next, the mold is closed by the mold opening/closing device.The mold opening/closing device is not shown in the figure, but in normal cases, it is connected to the guide plate to which the mold is attached. It consists of a hydraulic cylinder, and the movement of the hydraulic cylinder moves the Goui plate, opening and closing the mold.
次に、加熱工程に入る0通常の加熱操作では、両方のド
レン弁(28)(29)を開いた状態で、固定側蒸気弁
(19)と移動側蒸気弁(20)を開けて、固定側蒸気
室(17)と移動側蓋気室(1日)の空気と蒸気の置換
を行うと共に、固定側中型(12)と移動側中型(13
)の蒸気加熱を行う予備加熱操作に続いて、移動側蒸気
弁(20)と固定側ドレン弁(28)を閉め、固定側蒸
気弁(19)と移動側ドレン弁(29)を開けて行う一
方加熱操作、続いて固定側空気弁(19)と移動側ドレ
ン弁(29)を閉め、移動側蒸気弁(20)と固定側ド
レン弁(28)を開けて行う逆一方加熱操作により成形
体の内部加熱融着を行い、更に、両方のドレン弁(2B
)(29)を閉めて両方の蒸気弁(19)(20)を開
けて行う両面加熱により表面の加熱融着を行う0次に蒸
気供給を止めて、ドレン弁(28)(29)を閉じた状
態で数秒間維持して保熱する。これは成形体の全体を均
一融着させると共に、フレーム(lO)(11)の外側
からの放熱により、内部の加熱した残留蒸気圧の低下に
も役立っている。Next, the heating process begins.0 In normal heating operation, with both drain valves (28) and (29) open, the fixed side steam valve (19) and moving side steam valve (20) are opened, and the fixed side steam valve (19) and moving side steam valve (20) are opened. In addition to replacing the air and steam in the side steam room (17) and the moving side lid air chamber (1st), the fixed side medium size (12) and the moving side medium type (13) are replaced.
), the moving side steam valve (20) and fixed side drain valve (28) are closed, and the fixed side steam valve (19) and moving side drain valve (29) are opened. One-sided heating operation, followed by reverse one-sided heating operation performed by closing the fixed side air valve (19) and moving side drain valve (29) and opening the moving side steam valve (20) and fixed side drain valve (28), the molded product Then, both drain valves (2B
) (29) and open both steam valves (19) and (20) to heat and fuse the surfaces by double-sided heating. Next, stop the steam supply and close the drain valves (28) and (29). Hold it for a few seconds to keep it warm. This not only uniformly fuses the entire molded body, but also serves to lower the heated residual vapor pressure inside the frame (lO) (11) by dissipating heat from the outside.
次に冷却工程に入る。先ず、予冷操作であってドレン弁
(28)(29)を閉じた状態で固定側冷却水弁(21
)及び移動側冷却水弁(22)を開けて、数秒間冷却を
行う、この操作は両方のドレン弁(2B)(29)を開
けるとフレーム(10)(11)内部の残留蒸気が瞬時
に大気中に開放されるために生じる異常高音発生の防止
を目的としている0次いで、水冷操作であって10両方
のドレン弁(28)(29)を開けた状態で両方の冷却
水弁(21)(22)を開けて、固定側中型(12)及
び移動側中型(13)を水冷却することにより成形体室
(16)内の成形体の発泡圧力を低下させる0時間は成
形体の大きさ、発泡倍率、中型(12)(13)の構造
により一定ではないが、数10〜数100秒間が一般的
である。Next, the cooling process begins. First, in the pre-cooling operation, the fixed side cooling water valve (21) is opened with the drain valves (28) and (29) closed.
) and moving-side cooling water valve (22) to cool down for a few seconds. This operation can be done by opening both drain valves (2B) (29) and removing residual steam inside the frames (10) and (11). The purpose is to prevent abnormal high-pitched sounds caused by exposure to the atmosphere.Next, water cooling operation is performed with both drain valves (28) and (29) open, and both cooling water valves (21). (22) is opened and the fixed side middle mold (12) and moving side middle mold (13) are cooled with water to reduce the foaming pressure of the molded body in the molded body chamber (16). Time 0 is the size of the molded body. The foaming ratio is not constant depending on the structure of the medium size (12) (13), but it is generally several tens to several hundred seconds.
次に、通常行っている離型昇圧を先ず行う、即ち、型閉
の状態でドレン弁の固定側(28)及び移動側(29)
を閉じた状態で両方の蒸気室に空気加圧を行う、具体的
な操作としては固定側空気弁(23)及び移動側空気弁
(24)を開けることによって行う、操作条件としては
、時間は約2〜3秒間、圧力としては約0.5〜1.0
kg/dGであり、この操作により成形体を金型より外
れ易い状態にした後で、空気弁の固定側(23)及び移
動側(24)を止めると共にドレン弁の固定側(28)
及び移動側(29)を開放して金型内の圧力を抜く、中
型の形状は一般的には固定側中型(12)は凹型、移動
側中型(13)は凸型で、成形体は凹型と凸型の中間部
の成形室(16)にある。Next, the normal mold release pressure is increased first, that is, with the mold closed, the drain valves are connected to the fixed side (28) and moving side (29).
Pressure is applied to both steam chambers with the air valve closed.The specific operation is to open the fixed side air valve (23) and the moving side air valve (24).The operating conditions are as follows: For about 2 to 3 seconds, the pressure is about 0.5 to 1.0
kg/dG, and after this operation makes it easy for the molded object to be removed from the mold, the fixed side (23) and moving side (24) of the air valve are stopped, and the fixed side (28) of the drain valve is stopped.
And the moving side (29) is opened to release the pressure inside the mold. Generally speaking, the shape of the middle mold is that the fixed side middle mold (12) is concave, the moving side middle mold (13) is convex, and the molded body is concave. and the molding chamber (16) in the middle of the convex shape.
次に成形体を固定側中型(12)から移動側中型(13
)へ若干量移動させるために、両方のドレン弁(2B)
(29)を閉めて、移動側真空弁(26)を開けて真空
減圧にすると共に、固定側空気弁(23)を開けて加圧
状態にする。約3〜8秒後に固定側空気弁(23)を閉
めて型開きを行うことにより、上記の作用により成形体
は移動側中型(13)側に吸引移動する。第3図に示す
成形体の立上り部(a)が固定側中型(12)から外れ
ない程度にして型開きを止める。この型開きスローの操
作を行うことにより、成形体は固定側中型(12)から
ピン割れを起こさずに容易に離型されるようになる。具
体的には、ピン割れを起こさない面圧の最高値は、従来
の離型方法では0.3〜0.4kg/edGであるのに
対し、本発明では0.7〜1.0kg/dGである。Next, the molded body is transferred from the fixed side middle mold (12) to the moving side middle mold (13).
), both drain valves (2B)
(29), open the movable side vacuum valve (26) to reduce the pressure, and open the stationary side air valve (23) to pressurize it. After about 3 to 8 seconds, the stationary side air valve (23) is closed and the mold is opened, and the molded body is suctioned and moved toward the movable middle mold (13) by the above action. The mold opening is stopped to such an extent that the rising portion (a) of the molded body shown in FIG. 3 does not come off from the stationary middle mold (12). By carrying out this mold opening throw operation, the molded article can be easily released from the stationary middle mold (12) without causing pin cracks. Specifically, the maximum value of the surface pressure that does not cause pin cracking is 0.3 to 0.4 kg/edG in the conventional mold release method, whereas it is 0.7 to 1.0 kg/edG in the present invention. It is.
次に、型閉めを行うことにより成形体は再び固定側中型
(12)に固着される。もっとも、この型閉めを省略し
て直ちに次の離型取出し操作に入ることもできる。Next, by closing the mold, the molded body is again fixed to the stationary middle mold (12). However, it is also possible to omit this mold closing and immediately proceed to the next mold release/removal operation.
上記の成形体を固定側中型(12)から移動側中型(1
3)側に移動させる操作において、下記の方法も採用で
きる。即ち、成形体が固定側中型(12)に残留できる
位置まで吸引密着移動させた後に、移動側真空弁(26
)を止めて、移動側空気弁(24)を開けて移動側蒸気
室(18)を加圧状態にすることにより、成形体を固定
側中型(12)に残留させる。The above molded body is transferred from the fixed side middle mold (12) to the moving side middle mold (1
3) In the operation of moving to the side, the following method can also be adopted. That is, after the molded body is suctioned and moved to a position where it can remain in the stationary middle mold (12), the movable side vacuum valve (26) is moved.
) and open the moving side air valve (24) to pressurize the moving side steam chamber (18), thereby leaving the molded body in the stationary side middle mold (12).
尚、真空装置は、公知の真空ポンプ、蒸気や水のインゼ
クター等を使用できる。As the vacuum device, a known vacuum pump, steam or water injector, etc. can be used.
次の離型取出し操作は、従来より行っている離型方法で
あって、型開きスロー操作は型開きしながら、固定側ド
レン弁(28)及び移動側ドレン弁(29)を閉めて固
定側空気弁(23)を開けて、固定側中型(12)から
成形体が離型し易くし、次の段階では少し型が開いた状
態で移動側ドレン弁(29)を開けて型開きを続行し、
最終的に固定側中型(12)に在る成形体をエゼクトピ
ン(9)で離型押出す。The next mold release operation is a conventional mold release method, and the mold opening slow operation is performed by closing the fixed side drain valve (28) and moving side drain valve (29) while opening the mold. Open the air valve (23) to make it easier for the molded product to be released from the stationary middle mold (12), and in the next step, open the movable side drain valve (29) with the mold slightly open to continue opening the mold. death,
Finally, the molded body in the fixed-side middle mold (12) is released and extruded using an eject pin (9).
以下、本発明を実施例を挙げて説明するが、本発明はこ
れらに限定されないことは勿論である。The present invention will be described below with reference to Examples, but it goes without saying that the present invention is not limited thereto.
実施例1.2、比較例1.2
(1)使用樹脂
エチレン−プロピレンランダムコポリマー(エチレン含
有率3.5重量%)
(2)予備発泡方法及び発泡剤
前記に説明した方法で発泡剤はトリクロロトリフルオロ
エタン
(3)成形体
自動車用バンパー芯材
全長1540mmX巾158mmx高さ98m+a第1
表に示す条件で成形体を製造し、ピン割れを起こさない
程度に冷却した後に成形体を取出し、冷却時間と成形サ
イクルとを測定した。Example 1.2, Comparative Example 1.2 (1) Resin used ethylene-propylene random copolymer (ethylene content 3.5% by weight) (2) Pre-foaming method and blowing agent The blowing agent was trichloro in the method explained above. Trifluoroethane (3) molded body Bumper core material for automobiles Total length 1540mm x Width 158mm x Height 98m + a 1st
Molded bodies were manufactured under the conditions shown in the table, and after cooling to an extent that did not cause pin cracking, the molded bodies were taken out and the cooling time and molding cycle were measured.
結果を第1表に示したが、本発明の実施例はいずれも対
応する比較例に比べて、冷却時間及び成形サイクルとも
大巾に短縮された。The results are shown in Table 1, and the cooling time and molding cycle of all the examples of the present invention were significantly shortened compared to the corresponding comparative examples.
ポリオレフィン発泡体は従来の方法では離型押出し時に
ピン割れが発生し易いという問題があるため、離型抵抗
の原因になっている面圧(発泡力)を低下させるための
充分な冷却時間が必要である。従って、冷却時間を短縮
することは非常に困難であったが、本発明により真空吸
引力を主体とし、必要に応じて圧縮空気を併用して成形
体を固定側金型から移動側空気弁りに若干(1m−10
閣)移動させてから離型押出しすることにより、ピン割
れ等の損傷なく冷却時間を大巾に短縮して取出すことが
でき、成形生産性を飛躍的に増大させることができる。With conventional methods, polyolefin foams are prone to pin cracking during mold release extrusion, so sufficient cooling time is required to reduce the surface pressure (foaming force) that causes mold release resistance. It is. Therefore, it was very difficult to shorten the cooling time, but with the present invention, vacuum suction is used as the main force, and compressed air is also used as needed to move the molded product from the stationary mold to the movable air valve. (1m-10
By extruding the mold after moving it, the cooling time can be greatly shortened and the mold can be taken out without damage such as pin cracking, and molding productivity can be dramatically increased.
第1図は金型の一例を示す概要図、第2図(A)、CB
)はピン割れの状態を示す説明図で、(A)は側面図、
(B)は上面図、第3図は本発明に用いられる装置の一
例を示す概要図である。
!・・・予備発泡粒子、 2・・・ホッパー3・
・・シャッター 4・・・シャンター開閉弁5
・・・ホース、
7・・・フィーダー開閉弁、
9・・・エゼクトピン、
11・・・移動側フレーム、
13・・・移動側中型、
15・・・移動側スリット、
17・・・固定側蒸気室、
19・・・固定側蒸気弁、
21・・・固定側冷却水弁、
23・・・固定側空気弁、
25・・・固定側真空弁、
27・・・真空装置、
29・・・移動側ドレン弁、
31・・・成形体、
6・・・フィーダー
8・・・充填用空気弁
10・・・固定側フレーム
12・・・固定側中型
14・・・固定側スリット
16・・・成形体室
18・・・移動側蒸気室
20・・・移動側蒸気弁
22・・・移動側冷却水弁
24・・・移動側空気弁
26・・・移動側真空弁
28・・・固定側ドレン弁
30・・・排水管
32・・・割れFigure 1 is a schematic diagram showing an example of a mold, Figure 2 (A), CB
) is an explanatory diagram showing the state of pin cracking, (A) is a side view,
(B) is a top view, and FIG. 3 is a schematic diagram showing an example of the device used in the present invention. ! ... Pre-expanded particles, 2... Hopper 3.
...Shutter 4...Shunter on-off valve 5
... Hose, 7... Feeder on-off valve, 9... Eject pin, 11... Moving side frame, 13... Moving side medium size, 15... Moving side slit, 17... Fixed side steam Chamber, 19... Fixed side steam valve, 21... Fixed side cooling water valve, 23... Fixed side air valve, 25... Fixed side vacuum valve, 27... Vacuum device, 29... Moving side drain valve, 31...Molded object, 6...Feeder 8...Filling air valve 10...Fixed side frame 12...Fixed side medium mold 14...Fixed side slit 16... Molded object chamber 18...Movable side steam chamber 20...Movable side steam valve 22...Movable side cooling water valve 24...Movable side air valve 26...Movable side vacuum valve 28...Fixed side Drain valve 30...Drain pipe 32...Cracked
Claims (1)
際し、成形体を離型取出しする前に移動側金型を真空減
圧にして成形体を移動側金型に吸引密着させながら型開
きした後に型閉めを行い、移動側金型を大気圧にすると
共に成形体を固定側金型に移した後、離型取出しするこ
とにより冷却時間を短縮することを特徴とするオレフィ
ン系樹脂発泡体の製造方法。 2、オレフィン系樹脂粒子から発泡成形体を製造するに
際し、成形体を離型取出しする前に移動側金型を真空減
圧にして成形体を吸引密着させながら成形体が固定側金
型に残留できる位置まで型開きした後、移動側金型を大
気圧にすることにより冷却時間を短縮することを特徴と
するオレフィン系樹脂発泡成形体の製造方法。 3、成形体の離型時の面圧(発泡圧)が0.4kg/c
m^2G以上で成形体を離型取出すことを特徴とする請
求項1又は2記載の製造方法。[Claims] 1. When producing a foamed molded article from olefin resin particles, before removing the molded article from the mold, the movable mold is vacuumed and the molded article is brought into close contact with the movable mold by suction. The olefin-based product is characterized by shortening the cooling time by opening the mold, closing the mold, bringing the movable mold to atmospheric pressure, transferring the molded product to the stationary mold, and then removing it from the mold. Method for manufacturing resin foam. 2. When manufacturing a foamed molded product from olefin resin particles, before removing the molded product from the mold, the movable mold is vacuumed to bring the molded product into close contact with suction, allowing the molded product to remain in the stationary mold. A method for producing an olefin resin foam molded article, characterized in that after the mold is opened to the position, the cooling time is shortened by bringing the movable mold to atmospheric pressure. 3. Surface pressure (foaming pressure) when releasing the molded product is 0.4 kg/c
3. The manufacturing method according to claim 1, wherein the molded body is removed from the mold at m^2G or higher.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1082465A JPH02258327A (en) | 1989-03-31 | 1989-03-31 | Manufacture of olefin resin foam molded material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1082465A JPH02258327A (en) | 1989-03-31 | 1989-03-31 | Manufacture of olefin resin foam molded material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02258327A true JPH02258327A (en) | 1990-10-19 |
Family
ID=13775258
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1082465A Pending JPH02258327A (en) | 1989-03-31 | 1989-03-31 | Manufacture of olefin resin foam molded material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02258327A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111688097A (en) * | 2020-06-29 | 2020-09-22 | 倪威武 | Method for improving quality of foamed plastic material |
-
1989
- 1989-03-31 JP JP1082465A patent/JPH02258327A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111688097A (en) * | 2020-06-29 | 2020-09-22 | 倪威武 | Method for improving quality of foamed plastic material |
CN111688097B (en) * | 2020-06-29 | 2021-09-10 | 鹤山市盛世光华隔热材料有限公司 | Method for improving quality of foamed plastic material |
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