JPH0338967B2 - - Google Patents
Info
- Publication number
- JPH0338967B2 JPH0338967B2 JP57001744A JP174482A JPH0338967B2 JP H0338967 B2 JPH0338967 B2 JP H0338967B2 JP 57001744 A JP57001744 A JP 57001744A JP 174482 A JP174482 A JP 174482A JP H0338967 B2 JPH0338967 B2 JP H0338967B2
- Authority
- JP
- Japan
- Prior art keywords
- mold
- resin
- female
- molding
- foaming
- 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
- 229920005989 resin Polymers 0.000 claims description 69
- 239000011347 resin Substances 0.000 claims description 69
- 238000000465 moulding Methods 0.000 claims description 32
- 238000005187 foaming Methods 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 17
- 239000004604 Blowing Agent Substances 0.000 claims description 10
- 229920003002 synthetic resin Polymers 0.000 claims description 7
- 239000000057 synthetic resin Substances 0.000 claims description 7
- 229920001169 thermoplastic Polymers 0.000 claims description 6
- 239000004416 thermosoftening plastic Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 4
- 238000007789 sealing Methods 0.000 claims 1
- 239000006260 foam Substances 0.000 description 11
- 238000001746 injection moulding Methods 0.000 description 10
- 238000001125 extrusion Methods 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000011324 bead Substances 0.000 description 4
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000004088 foaming agent Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000463 material Substances 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
- -1 polyethylene Polymers 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002826 coolant Substances 0.000 description 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 2
- 238000010097 foam moulding Methods 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 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
- 239000004677 Nylon Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 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
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 229940042935 dichlorodifluoromethane Drugs 0.000 description 1
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 description 1
- 229960003750 ethyl chloride Drugs 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
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229940073584 methylene chloride Drugs 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
- 239000004431 polycarbonate resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 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
- 239000002994 raw material Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000454 talc Chemical class 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C44/00—Shaping by internal pressure generated in the material, e.g. swelling or foaming ; Producing porous or cellular expanded plastics articles
- B29C44/34—Auxiliary operations
- B29C44/36—Feeding the material to be shaped
- B29C44/38—Feeding the material to be shaped into a closed space, i.e. to make articles of definite length
Landscapes
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
本発明は金型を使用して発泡熱可塑性合成樹脂
成形品を原料樹脂から一挙に製造する方法に関す
るものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a foamed thermoplastic synthetic resin molded article from raw resin all at once using a mold.
金型を使用して発泡熱可塑性合成樹脂成形品を
製造する方法としては、いわゆるビーズ成形法と
発泡射出成形法が代表的なものである。しかしな
がら、ビーズ成形法は原料樹脂粒子を予備発泡さ
せて得られたビーズを金型内で加熱して2次発泡
させながら融着させて形成するという2段の発泡
工程を含むため、操作が煩雑であるばかりでな
く、ビーズを金型内の狭い隙間に送り込むのが難
しいから複雑な形状の成形を行うことはできない
という欠点がある。また射出成形法は、一段で発
泡成形品を得られるものの、通常の非発泡樹脂の
射出成形ほど容易に実施できる方法ではない。す
なわち、この方法のうち、金型キヤビテイにその
容積よりも少ない量の発泡性溶融樹脂を射出し、
射出直後から発泡して体積を増した樹脂により金
型キヤビテイを満たすシヨートシヨツト法では、
発泡倍率が思うように上らず、また成形品の“肌
荒れ”を起こし易い。また金型キヤビテイを発泡
性溶融樹脂で満たしたのち、金型の一方を移動さ
せることにより金型キヤビテイを拡大して樹脂を
発泡させるフルシヨツト法の場合は、成形装置が
複雑で高価なものとなるのが避けられないだけで
なく、成形中に型を移動させる必要上、成形品の
形状が制限されてしまう。しかも型の移動による
キヤビテイ拡大の影響を強く受ける部分とそうで
ない部分とで発泡倍率に差を生じ、発泡倍率した
がつて表面特性及び物性が一様でない成形品とな
り易い。以上の理由により、射出成形法によると
きは、十分高い強度を要求される成形品(例えば
構造材用発泡成形品)の場合、発泡倍率を高くす
ることができないという問題があつた。 Typical methods for producing foamed thermoplastic synthetic resin molded articles using a mold include so-called bead molding method and foaming injection molding method. However, the bead molding method involves a two-step foaming process in which beads obtained by pre-foaming raw resin particles are heated in a mold and fused while secondary foaming occurs, making the operation complicated. In addition, it is difficult to feed the beads into narrow gaps within the mold, making it impossible to mold complex shapes. In addition, although the injection molding method allows a foamed molded product to be obtained in one step, it is not as easy to carry out as ordinary injection molding of non-foamed resins. That is, in this method, an amount of foamable molten resin is injected into the mold cavity in an amount smaller than the volume of the mold cavity,
In the shot shot method, the mold cavity is filled with resin that expands and increases in volume immediately after injection.
The foaming ratio does not increase as expected, and the molded product tends to become rough. Furthermore, in the case of the full shot method, in which the mold cavity is filled with foamable molten resin and then one side of the mold is moved to expand the mold cavity and foam the resin, the molding equipment becomes complicated and expensive. Not only is this unavoidable, but the shape of the molded product is restricted due to the need to move the mold during molding. Moreover, there is a difference in the expansion ratio between parts that are strongly affected by cavity expansion due to mold movement and parts that are not, and as a result, the molded product tends to have uneven surface characteristics and physical properties. For the above reasons, when injection molding is used, there is a problem in that it is not possible to increase the expansion ratio in the case of molded products that require sufficiently high strength (for example, foam molded products for structural materials).
本発明は上記従来の合成樹脂型内発泡成形法の
ような欠点のない発泡成形法を提供することを目
的とするものである。 An object of the present invention is to provide a foam molding method that does not have the drawbacks of the conventional synthetic resin in-mold foam molding methods.
上記目的を達成することに成功した本発明につ
きまずその概要を述べると、形成面を包囲するシ
リンダ状部分を持つ雌型と該雌型のシリンダ状部
分に液封性嵌合が可能なピストン状部分を有する
雄型とからなる金型の雌型をその成形面上に溶融
状態の成形用樹脂を保持し得る姿勢で支持し、発
泡剤を含有する熱可塑性合成樹脂の溶融物を上記
雌型の成形面上に供給して常圧において到達可能
な最大発泡倍率の50%以上かつ意図する成形品の
発泡倍率よりも大きい発泡倍率まで発泡させ、次
いで雌型のシリンダ状部分に雄型を嵌入させて所
定の金型キヤビテイを完成させるとともにその過
程で雌型内の発泡樹脂溶融物を圧縮し、その後金
型を冷却し、硬化した発泡樹脂を金型より取出す
ことを特徴とするものである。 The present invention, which has succeeded in achieving the above object, will first be summarized as follows: a female mold having a cylindrical portion surrounding the forming surface; A female die of a mold consisting of a male die and a male die having a part is supported in a position capable of holding a molten molding resin on its molding surface, and a molten thermoplastic synthetic resin containing a blowing agent is placed in the female die. The foam is supplied onto the molding surface of the mold and foamed to a foaming ratio of 50% or more of the maximum foaming ratio that can be achieved at normal pressure and larger than the foaming ratio of the intended molded product, and then the male mold is inserted into the cylindrical part of the female mold. The method is characterized in that a predetermined mold cavity is completed, and in the process, the foamed resin melt in the female mold is compressed, the mold is then cooled, and the hardened foamed resin is taken out from the mold. .
以下、本発明をその実施のための装置の一例の
概略を示す図面を参照しながら詳しく説明する。 DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described in detail below with reference to drawings schematically showing an example of an apparatus for carrying out the invention.
第1図において、1は押出機、2は雌型、3は
雄型である。雌型2は、直立壁21を持つ浅い箱
状体22の底板23上に断面凸字状の雌型構成ユ
ニツト4を3個敷き詰めてそれらの表面を成形面
41としたものである。一方、雄型3は、平らな
基板31に断面凹字状の雄型構成ユニツト5を3
個、密着配置で固着したものである。雌型2と雄
型3は、後者の雄型構成ユニツト5群の外周32
と前者の直立壁21の内周面24とが、全周にわ
たりピストンとシリンダの関係で密に(空気は逃
すが溶融樹脂は漏らさない程度に密に)嵌合する
ようになつている。そして、上記嵌合を完成した
状態において、各雌型構成ユニツト4と雄型構成
ユニツト5との間に箱状の金型キヤビテイ(後記
第3図において樹脂溶融物6で満たされている部
分)が形成され、1回に3個の箱が成形されるよ
うになつている。雌型2は、成形開始時には図示
したように押出機の押出ダイス11の下方にある
が、水平方向に移動可能な支持機構(図示せず)
により支持されている。一方雄型3は雌型2が図
面左方へ移動したとき降下してこれと合体し得る
位置に、昇降機構を備えた支持手段(図示せず)
により支持されている。各金型は熱媒(又は冷
媒)を用いて加熱(又は冷却)することができ、
成形開始時には加熱されている。 In FIG. 1, 1 is an extruder, 2 is a female mold, and 3 is a male mold. The female mold 2 has three female mold constituent units 4 each having a convex cross-section on a bottom plate 23 of a shallow box-like body 22 having an upright wall 21, and their surfaces serve as molding surfaces 41. On the other hand, the male mold 3 has a male mold constituent unit 5 having a concave cross section on a flat substrate 31.
They are fixed in close contact with each other. The female mold 2 and the male mold 3 are connected to the outer periphery 32 of the latter male mold constituent unit 5 group.
and the inner circumferential surface 24 of the former upright wall 21 are tightly fitted over the entire circumference in a piston-cylinder relationship (tightly enough to allow air to escape but not to leak molten resin). Then, in the state in which the above-mentioned fitting is completed, a box-shaped mold cavity (the part filled with resin melt 6 in FIG. 3 described later) is formed between each female mold component unit 4 and male mold component unit 5. is formed, and three boxes are molded at one time. At the start of molding, the female mold 2 is located below the extrusion die 11 of the extruder as shown in the figure, but is supported by a support mechanism (not shown) that is movable in the horizontal direction.
Supported by On the other hand, the male mold 3 is provided with a support means (not shown) equipped with a lifting mechanism at a position where it can be lowered and combined with the female mold 2 when it moves to the left in the drawing.
Supported by Each mold can be heated (or cooled) using a heating medium (or cooling medium),
It is heated at the start of molding.
この装置を用いて成形を行う場合は、成形用樹
脂をホツパー12により押出機1に供給し、また
溶剤型発泡剤を発泡剤圧入口13より圧入して両
者を加熱・加圧下に混合する。溶融した樹脂と発
泡剤とからなる発泡性用溶融樹脂は断面が円形の
吐出口を有する押出ダイス11から空気中へ、太
い糸条状に押出され、直ちに下方の雌型2の成形
面41に受止められる。このとき、屈曲可能な押
出ダイス取付管14に装着された押出ダイス11
及び雌型2の一方又は両方を少しずつ移動させ
て、成形に十分な量の発泡性溶融樹脂を成形面4
1のなるべく全面に付着させる。 When molding is carried out using this apparatus, a molding resin is supplied to the extruder 1 through a hopper 12, and a solvent-based blowing agent is press-fitted through a blowing agent injection port 13, and both are mixed under heat and pressure. The molten resin for foaming, which is made up of molten resin and a foaming agent, is extruded into the air from an extrusion die 11 having a discharge port with a circular cross section in the form of a thick thread, and is immediately applied to the molding surface 41 of the female mold 2 below. It is accepted. At this time, the extrusion die 11 attached to the bendable extrusion die attachment pipe 14
and the female mold 2 little by little to apply a sufficient amount of foamable molten resin to the molding surface 4.
Apply it to the entire surface of 1 as much as possible.
樹脂の供給を終つたならば直ちに雌型2を雄型
3の直下に移動させる。 Immediately after supplying the resin, the female mold 2 is moved directly below the male mold 3.
発泡性溶融樹脂は加熱された成形面41上で直
ちに発泡を開始するから、成形面41はやがて発
泡した樹脂溶融物で覆われる(第2図にこの状態
を拡大して示した。同図中、6が発泡した溶融樹
脂である。)。 Since the foamable molten resin immediately starts foaming on the heated molding surface 41, the molding surface 41 is soon covered with the foamed molten resin (this state is shown in an enlarged manner in FIG. 2. , 6 is the foamed molten resin).
樹脂の発泡が常圧において到達可能な最大発泡
倍率の50%以上、好ましくは60〜80%の発泡度に
達しかつ意図する成形品の発泡倍率よりも大きい
発泡倍率に達したならば、雄型構成ユニツト5群
のピストン状外周面32を雌型2のシリンダ状内
周面24に沿わせながら雄型3を降下させて雄型
3を雌型2に嵌入させ、合体させる。第3図に示
したように、合体により形成された金型キヤビテ
イはそれが形成される過程で発泡した溶融樹脂6
により満たされるが、雌型2と雄型3の嵌合が上
述のように溶融樹脂を漏らさない密な嵌合である
ことにより、樹脂の供給量が過小でない限り、金
型キヤビテイ完成前に必ず発泡溶融樹脂の圧縮が
起こる。発泡溶融樹脂が圧縮されると、理由は定
かでないが発泡力が強くなるので、発泡樹脂は金
型キヤビテイの隅々までゆきわたつて均一な組織
の発泡成形体を生じる。また、表面は両金型のキ
ヤビテイ成形面に強く押し付けられて、緻密な表
皮層が形成されることになる。なお、圧縮が行わ
れることにより、最終的に得られる発泡成形体の
発泡倍率は雄型による圧縮開始前において溶融樹
脂が到達した最高発泡倍率よりも低くなる。 When the foaming of the resin reaches 50% or more of the maximum foaming ratio that can be achieved at normal pressure, preferably 60 to 80%, and the foaming ratio is greater than the foaming ratio of the intended molded product, the male mold The male die 3 is lowered while the piston-shaped outer circumferential surface 32 of the constituent units 5 groups is aligned with the cylindrical inner circumferential surface 24 of the female die 2, and the male die 3 is fitted into the female die 2 and combined. As shown in Figure 3, the mold cavity formed by the combination is made of molten resin 6 that is foamed during the process of formation.
However, since the fit between the female mold 2 and the male mold 3 is a tight fit that does not leak the molten resin as described above, unless the amount of resin supplied is too small, it must be filled before the mold cavity is completed. Compression of the foamed molten resin occurs. When the foamed molten resin is compressed, the foaming force increases for reasons that are not clear, so the foamed resin spreads to every corner of the mold cavity, producing a foamed molded product with a uniform structure. Furthermore, the surface is strongly pressed against the cavity molding surfaces of both molds, forming a dense skin layer. Note that, by performing the compression, the expansion ratio of the finally obtained foamed molded product becomes lower than the maximum expansion ratio reached by the molten resin before the compression by the male die is started.
この後、金型に対する熱媒の供給を停止し、冷
媒を供給して金型を冷却することにより発泡樹脂
6を冷却し硬化させる。硬化終了後、雄型3を上
昇させて雌型2と分離し、硬化し且つ成型された
発泡樹脂を金型から取出す。 Thereafter, the supply of heat medium to the mold is stopped, and a coolant is supplied to cool the mold, thereby cooling and hardening the foamed resin 6. After curing, the male mold 3 is raised and separated from the female mold 2, and the cured and molded foamed resin is taken out from the mold.
上述のような本発明の製法を実施する場合、押
出機で調製した発泡性溶融樹脂は上記例のように
直接金型に供給するほか、一旦加圧状態に保つた
貯槽に貯えてから逐次金型に供給してもよい。ま
た発泡性溶融樹脂は比較的細い糸条状又はテープ
状に押出し、産業用ロボツトを利用するなどして
これを金型の成形面全体に必要量ずつ付着させる
ことが望ましいが、単純な形状に形成する場合は
樹脂を比較的太い流れとして押出し、金型の成形
面の一部に、点状又は線状に付着させても差支え
ない。 When carrying out the manufacturing method of the present invention as described above, the foamable molten resin prepared in an extruder is not only directly supplied to the mold as in the above example, but also stored in a storage tank kept under pressure and then sequentially poured into the mold. It may also be fed into a mold. In addition, it is desirable to extrude the foamable molten resin into a relatively thin string or tape shape and apply it in the required amount to the entire molding surface of the mold using an industrial robot. When forming the mold, the resin may be extruded in a relatively thick flow and adhered to a part of the molding surface of the mold in dots or lines.
樹脂の押出し開始から金型の合体まで、金型は
それ自体を熱媒体又は電気ヒーターにより加熱す
るだけでなく、樹脂の温度と同程度の高温の雰囲
気に置いて樹脂の冷却を防止することが望まし
い。これは、金型の成形面上に置かれた溶融樹脂
が表面から急速に冷却されると表面付近の樹脂の
発泡が不十分になるほか、得られる成形品の表面
性状が悪化するからである。 From the start of extrusion of the resin to the joining of the mold, the mold itself is not only heated by a heat medium or an electric heater, but also placed in an atmosphere at a high temperature comparable to the temperature of the resin to prevent the resin from cooling. desirable. This is because if the molten resin placed on the molding surface of the mold is rapidly cooled from the surface, the foaming of the resin near the surface will not be sufficient, and the surface quality of the resulting molded product will deteriorate. .
本発明の方法により発泡成形品とすることがで
きる熱可塑性合成樹脂の例としては、ポリエチレ
ン、ポリプロピレン、エチレンと他のモノオレフ
イン類(例えばプロピレン)との共重合体、エチ
レンとビニル単量体(例えば酢酸ビニル)との共
重合体等のポリオレフイン系樹脂;ポリスチレ
ン、ABS樹脂等のスチレン系樹脂;その他ポリ
塩化ビニル樹脂、各種ナイロン樹脂、ポリカーボ
ネート樹脂、ポリヒドロキシエーテル樹脂等があ
る。 Examples of thermoplastic synthetic resins that can be made into foam molded products by the method of the present invention include polyethylene, polypropylene, copolymers of ethylene and other monoolefins (e.g. propylene), and copolymers of ethylene and vinyl monomers (e.g. propylene). Examples include polyolefin resins such as copolymers with vinyl acetate); styrene resins such as polystyrene and ABS resins; other polyvinyl chloride resins, various nylon resins, polycarbonate resins, and polyhydroxyether resins.
また上記樹脂を発泡させるための発泡剤は分解
型発泡剤あるいは溶剤型発泡剤のいずれでもよい
が溶剤型のものが好ましく、特に好ましい具体例
にはシクロブタン、シクロペンタン等の環式脂肪
族炭化水素類;プロパン、ブタン、ペンタン、ヘ
キサン、ヘプタン等の脂肪族炭化水素類;トリク
ロロフルオロメタン、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、メチルクロ
ライド、エチルクロライド、メチレンクロライド
等のハロゲン化炭化水素類がある。なおこれらの
発泡剤と共に、発泡助剤たとえば有機酸の金属塩
もしくは水素金属塩、炭酸の金属塩もしくは水素
金属塩、タルク等を併用してもよい。 The blowing agent for foaming the above resin may be either a decomposable blowing agent or a solvent-type blowing agent, but a solvent-type blowing agent is preferable, and particularly preferable examples include cycloaliphatic hydrocarbons such as cyclobutane and cyclopentane. aliphatic hydrocarbons such as propane, butane, pentane, hexane, and heptane; halogenated hydrocarbons such as trichlorofluoromethane, dichlorodifluoromethane, dichlorotetrafluoroethane, methyl chloride, ethyl chloride, and methylene chloride. In addition to these foaming agents, foaming aids such as metal salts or hydrogen metal salts of organic acids, metal salts or hydrogen metal salts of carbonic acid, talc, etc. may be used in combination.
本発明の製造法において、原料樹脂、発泡剤及
び発泡助剤に必要に応じて他の材料を加えて押出
機中で溶融し発泡性溶融樹脂を調製する際の材料
配合比及び押出条件には、押出機が低圧のもので
済むことを除けば、従来の発泡射出成形の場合と
本質的な相違はない。したがつてこれらの条件に
ついての詳細な説明は省略する。 In the production method of the present invention, the material compounding ratio and extrusion conditions when preparing a foamable molten resin by adding other materials as necessary to the raw resin, blowing agent, and foaming aid and melting them in an extruder are as follows: There is no essential difference from conventional foam injection molding, except that the extruder requires a low pressure extruder. Therefore, a detailed explanation of these conditions will be omitted.
以上のような本発明の発泡成形品製造法は、従
来の発泡射出成形法と比べると次のような特長を
持つ。 The method for manufacturing a foam molded article of the present invention as described above has the following features compared to the conventional foam injection molding method.
閉鎖的な金型キヤビテイに発泡性溶融樹脂を
押込む射出成形と違つて一方の金型の開放的な
成形面上への樹脂を供給するのであるから、高
圧の押出装置を必要とせず、金型も耐圧性のも
のでなくてよい。したがつて成形装置全体が安
価なもので済むだけでなく、従来は成形困難で
あつたような大型の成形品も容易に製造するこ
とができる。 Unlike injection molding, in which foamable molten resin is forced into a closed mold cavity, the resin is supplied onto the open molding surface of one mold, so there is no need for high-pressure extrusion equipment, and the metal The mold does not need to be pressure resistant either. Therefore, not only can the entire molding apparatus be inexpensive, but also large molded products, which were conventionally difficult to mold, can be easily produced.
発泡性溶融樹脂を自由に発泡させたのち圧縮
成形するので、閉鎖的なキヤビテイ内で発泡さ
せる射出成形の場合よりも発泡が均一で緻密な
表面を持ち、しかも高発泡倍率の成形品を製造
することができる(射出成形法の場合、発泡倍
率を2倍以上にすることは難かしいが、本発明
の方法によれば容易に2〜10倍の発泡が可能で
ある。)。 Since the foamable molten resin is freely foamed and then compression molded, it produces molded products with more uniform foaming, a denser surface, and a higher expansion ratio than injection molding, which foams in a closed cavity. (In the case of injection molding, it is difficult to increase the expansion ratio to 2 times or more, but according to the method of the present invention, foaming can be easily increased from 2 to 10 times.)
金型に対する独特の樹脂供給法に基づき成形
面に沿う樹脂の流動を最小限にすることができ
るため、また実際に成形される発泡ずみ溶融樹
脂は未発泡(又は発泡開始直後の)溶融樹脂よ
りも流動性がよいため、得られる成形品は肌荒
れや筋模様のない美麗な表面を有し、物性面で
も斑がないから同じ発泡倍率の射出成形品に比
べると強度が大きい。 Based on the unique resin supply method to the mold, the flow of resin along the molding surface can be minimized, and the foamed molten resin that is actually molded is smaller than the unfoamed (or immediately after foaming) molten resin. Because it has good fluidity, the resulting molded product has a beautiful surface without roughness or streaks, and has no unevenness in terms of physical properties, so it is stronger than an injection molded product with the same expansion ratio.
上記と同じ理由により、射出成形法では到
底成形できないような複雑な形状のものでも成
形することができる。 For the same reason as mentioned above, it is possible to mold even complex shapes that cannot be molded by injection molding.
以下実施例を示して本発明を説明する。 The present invention will be explained below with reference to Examples.
実施例
第1図に示した装置と同様の装置を用いて縦
125mm、横190mm、高さ24mmの角皿状発泡成形品
(凹み部分の深さ20mm、縦100mm、横150mm)を製
造した。Example Using a device similar to that shown in Figure 1,
A rectangular plate-shaped foam molded product measuring 125 mm, width 190 mm, and height 24 mm (depth of concave portion 20 mm, length 100 mm, and width 150 mm) was manufactured.
原料樹脂としてはメルトインデツクス11の高
密度ポリエチレンを用い、これに発泡助剤として
クエン酸ソーダを0.1重量%(対樹脂重量)混合
したものをホツパーから押出機に供給し、別に発
泡剤圧入口から発泡剤(ジクロロジフルオロメタ
ン)を5重量%(対樹脂重量)圧入し、両者を
160℃に加熱して混練することにより発泡性溶融
樹脂を調製した。得られた溶融樹脂を屈曲可能な
管を通して口径8mmのダイスに送り、ここから糸
条状に押出して下方の雌型の成形面に垂下させ
た。金型は前記形状の成型品40個を一度に成形す
るための複合金型(5行×8列配置)であり、電
気ヒーターにより120℃に加熱しておいた。成形
面の水平部分1m2当り約200gの溶融樹脂を均一
に付着させたのち、樹脂の供給を停止し、雌型を
水平に移動させた。押出してから約2分後、溶融
樹脂が約5倍(常圧において到達可能な最大発泡
倍率の60%)に発泡したところで上記雌型に対応
する雄型を上方から降下させて両金型を合体さ
せ、直ちに金型の加熱を停止した。このあと冷却
水を金型冷却用管に送つて金型及び樹脂を冷却
し、10分後雄型を雌型からを分離して硬化した発
泡樹脂を取出した。 High-density polyethylene with a melt index of 11 is used as the raw material resin, and a mixture of 0.1% by weight (relative to resin weight) of sodium citrate as a foaming aid is supplied to the extruder from a hopper, and a foaming agent injection port is separately provided. 5% by weight (based on the weight of the resin) of a blowing agent (dichlorodifluoromethane) was injected into the
A foamable molten resin was prepared by heating to 160°C and kneading. The obtained molten resin was sent through a bendable tube to a die with a diameter of 8 mm, from which it was extruded in the form of a thread and suspended from the molding surface of the female mold below. The mold was a composite mold (5 rows x 8 columns arranged) for molding 40 molded products of the above shape at once, and was heated to 120° C. with an electric heater. After approximately 200 g of molten resin was uniformly deposited per 1 m 2 of the horizontal portion of the molding surface, the supply of resin was stopped and the female mold was moved horizontally. Approximately 2 minutes after extrusion, when the molten resin has expanded to approximately 5 times the foam (60% of the maximum foaming ratio that can be achieved at normal pressure), the male mold corresponding to the female mold is lowered from above to separate both molds. Immediately after combining, heating of the mold was stopped. After that, cooling water was sent to the mold cooling pipe to cool the mold and the resin, and after 10 minutes, the male mold was separated from the female mold and the hardened foamed resin was taken out.
得られた発泡成形品は緻密で一様なごく薄い表
皮層を持ち、表皮層以外の部分の発泡はきわめて
均一であり、平均発泡倍率は3.1倍であつた。 The resulting foamed molded product had a dense, uniform, and very thin skin layer, and the foaming in areas other than the skin layer was extremely uniform, and the average expansion ratio was 3.1 times.
第1図:本発明を実施するための装置の一例の
略図。第2図:第1図の雌型2上で樹脂溶融物が
発泡した状態を示す断面図。第3図:第1図の雌
型2及び同3が合体して発泡樹脂が成形された状
態を示す断面図。
1:押出機、2:雌型、3:雄型、41:成形
面、6:発泡した樹脂。
FIG. 1: Schematic representation of an example of an apparatus for carrying out the invention. FIG. 2: A sectional view showing a state in which the resin melt foams on the female mold 2 of FIG. 1. FIG. 3: A sectional view showing a state in which the female molds 2 and 3 of FIG. 1 are combined to mold a foamed resin. 1: Extruder, 2: Female mold, 3: Male mold, 41: Molding surface, 6: Foamed resin.
Claims (1)
と該雌型のシリンダ状部分に液封性嵌合が可能な
ピストン状部分を有する雄型とからなる金型の雌
型をその成形面上に溶融状態の成形用樹脂を保持
し得る姿勢で支持し、発泡剤を含有する熱可塑性
合成樹脂の溶融物を上記雌型の成形面上に供給し
て常圧において到達可能な最大発泡倍率の50%以
上かつ意図する成形品の発泡倍率よりも大きい発
泡倍率まで発泡させ、次いで雌型のシリンダ状部
分に雄型を嵌入させて所定の金型キヤビテイを完
成させるとともにその過程で雌型内の発泡樹脂溶
融物を圧縮し、その後金型を冷却し、硬化した発
泡樹脂を金型より取出すことを特徴とする発泡熱
可塑性合成樹脂成形品の製造法。1. A female die of a mold consisting of a female die having a cylindrical portion surrounding the molding surface and a male die having a piston-like portion capable of being fitted in a liquid-sealing manner to the cylindrical portion of the female mold is placed on the molding surface. The molding resin is supported in a position that can hold the molten molding resin, and a molten thermoplastic synthetic resin containing a blowing agent is supplied onto the molding surface of the female mold to achieve the maximum expansion ratio that can be achieved at normal pressure. The foaming is carried out to a foaming ratio of 50% or more and larger than the foaming ratio of the intended molded product, and then the male mold is fitted into the cylindrical part of the female mold to complete the specified mold cavity, and in the process, the inside of the female mold is A method for manufacturing a foamed thermoplastic synthetic resin molded article, which comprises compressing a foamed resin melt, cooling a mold, and taking out the hardened foamed resin from the mold.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57001744A JPS58119832A (en) | 1982-01-11 | 1982-01-11 | Manufacture of molded item of foamable thermoplastic synthetic resin |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57001744A JPS58119832A (en) | 1982-01-11 | 1982-01-11 | Manufacture of molded item of foamable thermoplastic synthetic resin |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58119832A JPS58119832A (en) | 1983-07-16 |
JPH0338967B2 true JPH0338967B2 (en) | 1991-06-12 |
Family
ID=11510070
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57001744A Granted JPS58119832A (en) | 1982-01-11 | 1982-01-11 | Manufacture of molded item of foamable thermoplastic synthetic resin |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58119832A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102013905B1 (en) * | 2019-03-29 | 2019-08-23 | 한국신발피혁연구원 | Manufacturing method of foam using the improved cmp process |
KR102249059B1 (en) * | 2020-01-30 | 2021-05-10 | 한국해양테크(주) | Buoy manufacturing and the buoy |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4934969A (en) * | 1972-08-04 | 1974-03-30 | ||
JPS5128869A (en) * | 1974-09-06 | 1976-03-11 | Ig Gijutsu Kenkyusho Kk | |
JPS5423671A (en) * | 1977-07-23 | 1979-02-22 | Nikko Plastic Kogyo | Method of molding synthetic resin foam article |
JPS5611090A (en) * | 1979-07-09 | 1981-02-04 | Kohkoku Chem Ind | Manufacture of cushion body |
-
1982
- 1982-01-11 JP JP57001744A patent/JPS58119832A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4934969A (en) * | 1972-08-04 | 1974-03-30 | ||
JPS5128869A (en) * | 1974-09-06 | 1976-03-11 | Ig Gijutsu Kenkyusho Kk | |
JPS5423671A (en) * | 1977-07-23 | 1979-02-22 | Nikko Plastic Kogyo | Method of molding synthetic resin foam article |
JPS5611090A (en) * | 1979-07-09 | 1981-02-04 | Kohkoku Chem Ind | Manufacture of cushion body |
Also Published As
Publication number | Publication date |
---|---|
JPS58119832A (en) | 1983-07-16 |
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