JPH0410914A - Method for mixing foamable agent into resin material - Google Patents
Method for mixing foamable agent into resin materialInfo
- Publication number
- JPH0410914A JPH0410914A JP11281590A JP11281590A JPH0410914A JP H0410914 A JPH0410914 A JP H0410914A JP 11281590 A JP11281590 A JP 11281590A JP 11281590 A JP11281590 A JP 11281590A JP H0410914 A JPH0410914 A JP H0410914A
- Authority
- JP
- Japan
- Prior art keywords
- raw material
- resin raw
- resin material
- mixed
- mixing
- 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
- 229920005989 resin Polymers 0.000 title claims abstract description 56
- 239000011347 resin Substances 0.000 title claims abstract description 56
- 238000002156 mixing Methods 0.000 title claims abstract description 21
- 238000000034 method Methods 0.000 title claims description 16
- 239000000463 material Substances 0.000 title abstract 11
- 238000003860 storage Methods 0.000 claims abstract description 23
- 238000010107 reaction injection moulding Methods 0.000 claims abstract description 11
- 239000002994 raw material Substances 0.000 claims description 82
- 239000004604 Blowing Agent Substances 0.000 claims description 23
- 239000004088 foaming agent Substances 0.000 abstract description 6
- 238000009834 vaporization Methods 0.000 abstract description 6
- 230000008016 vaporization Effects 0.000 abstract description 6
- 230000000694 effects Effects 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract 5
- 239000004814 polyurethane Substances 0.000 description 14
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 9
- 230000003068 static effect Effects 0.000 description 9
- 238000010586 diagram Methods 0.000 description 7
- 238000002347 injection Methods 0.000 description 7
- 239000007924 injection Substances 0.000 description 7
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 5
- 238000005187 foaming Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920003002 synthetic resin Polymers 0.000 description 4
- 239000000057 synthetic resin Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- AFYPFACVUDMOHA-UHFFFAOYSA-N chlorotrifluoromethane Chemical compound FC(F)(F)Cl AFYPFACVUDMOHA-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 229920006248 expandable polystyrene Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Landscapes
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Injection Moulding Of 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、合成樹脂原料に発泡剤を配合し−て反応射出
成形等により成形する場合の発泡剤の混入方法に関す番
尤のである。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method of mixing a blowing agent into a synthetic resin raw material and molding the mixture by reaction injection molding or the like.
(従来の技術−)
従来、ポリウレタン等の合成樹脂原料(以下、PU原料
という)を発泡、成形する場合、発泡剤としてフロンカ
スが使用されている。現在、フロンカスによるオゾン層
破壊とこれによる健康への悪影響か国際的に大きな間顕
となり、UNEP(国連環境計画)はCC0L (オゾ
ン間秋調整委員会)を組織して1985年3月に「オゾ
ン層保護のためのウィーン条約」を、1987年9月に
は「オゾン層を破壊する物質に関するモントリオール議
定書」を採択した。日本国政府も上記2条約に従い、1
988年5月に「フロン等規制法」を制定してフロンの
生産、使用規制に踏み出した。対象となるフロンカスは
、フロン−1112113114115の5種で、19
86年の生産、使用料を100として、1989年には
l 009を以下に、1993年には80%以下に、
1998年には50%以下に削減することになっている
。(Prior Art) Conventionally, when foaming and molding synthetic resin raw materials such as polyurethane (hereinafter referred to as PU raw materials), Froncas is used as a foaming agent. Currently, the depletion of the ozone layer by FFCs and its negative effects on health have become a major issue internationally, and UNEP (United Nations Environment Program) organized the CC0L (Ozone Interchange Coordination Committee) and announced in March 1985 that In September 1987, the Montreal Protocol on Substances that Deplete the Ozone Layer was adopted. In accordance with the above two treaties, the Japanese government also
In May 1988, the ``Freon Control Law'' was enacted to regulate the production and use of fluorocarbons. The target Froncas are 5 types of Freon-1112113114115, and 19
Taking production and usage fees in 1986 as 100, in 1989 it was less than l 009, and in 1993 it was less than 80%,
It is scheduled to be reduced to less than 50% in 1998.
フロンカスの主な用途は、(1)冷媒用、(2)エアゾ
ール用、(3)発泡用、(4)洗浄用であるが、(31
発泡用に関して言えば、使用対象を、(a)ウレタンフ
オームとtb+発泡ポリスチレン・発泡ボリオレフィン
とに分類することができ、発泡剤としてフロン−11,
12,114が主に使用されている。The main uses of Froncus are (1) for refrigerants, (2) for aerosols, (3) for foaming, and (4) for cleaning.
Regarding foaming, the objects to be used can be classified into (a) urethane foam and tb+ foamed polystyrene/foamed polyolefin.
12,114 are mainly used.
これらのフロンよりもオゾン破壊係数の低い代替品候補
としては、オゾン−22等が有力である9例えばオゾン
−22の場合、
(1)フロン−11のオゾン破壊力を1とした場合のオ
ゾン破壊係数は0.05
(2)発泡効率か良いので使用料がフロン−11の17
3でよい。As a candidate for a substitute with a lower ozone depletion coefficient than these CFCs, ozone-22 is a promising candidate9.For example, in the case of ozone-22, (1) Ozone depletion when the ozone depletion power of CFC-11 is set to 1. The coefficient is 0.05 (2) Since the foaming efficiency is good, the usage fee is 17 of Freon-11.
3 is fine.
(3)発泡製品の外観か向上する。(3) Improve the appearance of foamed products.
という利点がある。There is an advantage.
従来、例えばポリウレタン等の合成樹脂原料に発泡剤と
してフロンガスを混入、配合する場合、第7図に示すよ
うに、フロンポンベ2からPU原料4中に配管によりフ
ロンを導き、フロンを直接PU原料4に混入し、攪拌溶
解させて配合している。Conventionally, when mixing and blending fluorocarbon gas as a blowing agent into synthetic resin raw materials such as polyurethane, as shown in FIG. It is blended by stirring and dissolving.
(発明が解決しようとする課題)
しかしながら、上記のような方法では、投入されたフロ
ンカスが気泡としてPtJ原料4の液外13へ気化して
しまい、充分な混合、溶解がなされず、発泡剤としての
フロン(特にフロン−22)の配合が困難である。(Problem to be Solved by the Invention) However, in the above method, the introduced freon gas vaporizes as bubbles to the outside of the liquid 13 of the PtJ raw material 4, and is not sufficiently mixed and dissolved, so that it cannot be used as a blowing agent. It is difficult to blend Freon (especially Freon-22).
上記のようなフロンカス代替品の多くは、低沸点なので
、合成樹脂原料への混入に際し揮発ロスが多く、混入効
率か悪い、なお、代替品候補としてフロン−22は一4
1’C、フロン−13は一81’C、フoン−12Bl
は一4℃、7 o 7−142Bは一10℃ノ沸点を有
する。Most of the above-mentioned FFC substitutes have a low boiling point, so there is a lot of volatilization loss when mixed into synthetic resin raw materials, and the mixing efficiency is poor.
1'C, Freon-13 is -81'C, Freon-12Bl
has a boiling point of -4°C, and 7 o 7-142B has a boiling point of -10°C.
一方、ウレタンRIM成形(反応射出成形)等では、発
泡原材料の温度、粘度等の変動を防ぐために、原料を貯
留タンクと射出装置との間で絶えず循環させる方式が採
用されている。この循環は、外気に開放されない閉回路
内で行なわれるので、この回路中の戻り通路中へ前記フ
ロン−22を射出し、通路閉空間内でミキサーにより混
合して原料循環ルートに合流させ、さらに貯留タンク中
で2次攪拌することにより、発泡剤を原料中へ効率良く
混合させるのが良い、フロン−22の混入直後の原料は
フロン濃度が高く不安定で分離し易いので、直ちに貯留
タンク内の大量の原料中に導入して2次攪拌によりフロ
ン濃度を低下させ、混合状態を安定化させる必要がある
。それ故、循環回路中の前半部、すなわち貯留タンクか
ら射出装置に至る回路中にフロン−22を混入させるの
は適当ではない、この場合には、高濃度で不安定な混合
原料が曲折した回路内や射出装置の計量ポンプ内で分離
して不具合の原因になり易い。On the other hand, in urethane RIM molding (reaction injection molding) and the like, a method is adopted in which the raw material is constantly circulated between a storage tank and an injection device in order to prevent fluctuations in the temperature, viscosity, etc. of the foamed raw material. This circulation is carried out in a closed circuit that is not open to the outside air, so the Freon-22 is injected into the return path in this circuit, mixed by a mixer in the closed space of the path, and merged into the raw material circulation route. It is best to efficiently mix the blowing agent into the raw material by performing secondary stirring in the storage tank.The raw material immediately after the addition of Freon-22 has a high concentration of Freon, is unstable, and easily separates, so it should be mixed immediately into the storage tank. It is necessary to introduce the chlorofluorocarbon into a large amount of raw materials and perform secondary stirring to reduce the concentration of chlorofluorocarbons and stabilize the mixed state. Therefore, it is not appropriate to mix Freon-22 into the first half of the circulation circuit, that is, the circuit from the storage tank to the injection device. It is easy to separate inside the metering pump of the injection device and cause problems.
本発明は、前述のような従来の樹脂原料への発泡剤混入
方法の問題点に鑑み、発泡剤の気化を抑制し、樹脂原料
に発泡剤を効率良く混合できる方法を提供することを目
的とする。In view of the above-mentioned problems with the conventional method of mixing a blowing agent into a resin raw material, an object of the present invention is to provide a method that can suppress vaporization of the blowing agent and efficiently mix the blowing agent into a resin raw material. do.
(課懸を解決するための手段)
上記の目的を達成するため、本発明の樹脂原料への発泡
剤混入方法は、樹脂原料貯留容器と樹脂原料反応射出成
形装置との間に樹脂原料を循環させるための循環回路の
うち、樹脂原料反応射出成形装置から樹脂原料貯留容器
へ樹脂原料か回帰する戻り配管に発泡剤を射出し、戻り
配管中に配置された第1−ミキサーによって樹脂原料と
発泡剤とを1次混合し、この混合原料を樹脂原料貯留容
器内の樹脂原料へ進入させ、この樹脂原料貯留容器内に
おいて第2ミキサーによって2次混合するものである。(Means for solving the problem) In order to achieve the above object, the method of mixing a blowing agent into a resin raw material of the present invention circulates a resin raw material between a resin raw material storage container and a resin raw material reaction injection molding device. In the circulation circuit for this purpose, a foaming agent is injected into the return pipe that returns the resin raw material from the resin raw material reaction injection molding device to the resin raw material storage container, and the resin raw material and foam are foamed by the first mixer placed in the return pipe. This mixed raw material is introduced into the resin raw material in the resin raw material storage container, and is mixed secondarily in the resin raw material storage container by a second mixer.
(作用)
以上のように構成した本発明の方法によれば、樹脂原料
循環回路中の戻り配管中へ射出された発泡剤はその戻り
配管内と樹脂原料貯留容器内とで2段階に攪拌混合され
、発泡剤の気化が抑制されてWJ脂原料への発泡剤の混
合が効率良く行なわれる。(Function) According to the method of the present invention configured as described above, the blowing agent injected into the return pipe in the resin raw material circulation circuit is stirred and mixed in two stages: in the return pipe and in the resin raw material storage container. As a result, vaporization of the blowing agent is suppressed, and mixing of the blowing agent into the WJ fat raw material is performed efficiently.
(実施例)
以下、図面を参照して本発明の樹脂原料への発泡付混入
方法の実施例について説明する。(Example) Hereinafter, with reference to the drawings, an example of the method of foaming and mixing into a resin raw material of the present invention will be described.
第1図は、本発明の方法を実−施する装置の構成の一実
施例を示したもので、フロンの配合、混入は直接RIM
設備(1!!脂原料反応射出成形装置)20のPU原料
循環戻り配管1内において行なう構成とし、フロンボン
ベ2から戻り配管1に直接配管がなされている。Figure 1 shows an example of the configuration of an apparatus for carrying out the method of the present invention.
The PU raw material circulation return piping 1 of the equipment (1!! Fat raw material reaction injection molding apparatus) 20 is configured to carry out the process, and the fluorocarbon cylinder 2 is directly connected to the return piping 1.
タンク(樹脂原料貯留容器)3には、フロン以外の原料
、すなわちポリオール、架橋剤、触媒、整泡剤等が既に
配合されているPU原料4が投入されている。この際、
PU原料4はタンク3の容量に対して−多い方が良く、
できれば満杯とし、タンク内加圧は最低でも 1.5k
g/al1以上とし、例えば原料液温(通常20〜30
℃)のフロンの蒸気圧、本実施例のフロン−22では2
0℃で7kg/a#まで加圧することが望ましい。こう
することにより、投入されるフロンの気化が在る程度防
げて溶解が確実になる。A tank (resin raw material storage container) 3 is charged with a PU raw material 4 in which raw materials other than fluorocarbon, such as a polyol, a crosslinking agent, a catalyst, a foam stabilizer, etc. are already mixed. On this occasion,
The amount of PU raw material 4 is relative to the capacity of tank 3 - the more the better.
If possible, keep it full and pressurize the tank at least 1.5k.
g/al or more, for example, the raw material liquid temperature (usually 20 to 30
℃), the vapor pressure of Freon-22 in this example is 2
It is desirable to pressurize up to 7 kg/a# at 0°C. By doing this, vaporization of the introduced Freon can be prevented to some extent, and dissolution is ensured.
フロンの計量は、フロンボンベ2の残量又は流量計5に
より行なう。図示14はフロンボンベ2を計量する秤で
ある。フロンの混入は、配管中のバルブ6の開閉によっ
て行なわれる。バルブ6を通過したフロンは、チエツク
弁7を通ってPU原料循環戻り配管1へ約5〜50kz
/al!の圧力で注入され、直ちにスタティクミキサー
(第1ミキサー)8を通りタンク3に導入される。The amount of fluorocarbon is measured by the remaining amount in the fluorocarbon cylinder 2 or by the flowmeter 5. 14 is a scale for weighing the fluorocarbon cylinder 2. Freon is mixed in by opening and closing a valve 6 in the piping. The fluorocarbons that have passed through the valve 6 pass through the check valve 7 and are sent to the PU raw material circulation return pipe 1 at approximately 5 to 50 kz.
/al! The mixture is injected at a pressure of 1, and is immediately introduced into the tank 3 through a static mixer (first mixer) 8.
スタティックミキサー8は第2図にその断面を示したよ
うに、バイブ状機体の中に右ひねり、幇ひねつと交互に
逆になった複数のah状のエレメント9が配設されてい
る。このスタティックミキサー8内で、PU原料4とフ
ロンとはエレメント9に従って回転流動し、混合される
。第3図はこの回転流動の状態を図示したもので、10
は、右、左それぞれのエレメントでの回転、11は二つ
のエレメントでの回転を示している。スタティックミキ
サー8を通ることによりPtJ原料4とフロンとは効率
良く混合、溶解される。フロンの射出圧力は、PU原料
の粘度、液温により最適値か決定されるが、通常5〜1
50 kg/ dか望ましい、また、この時のPU原料
に対するフロンの混入割合は、PU原料1に対して0.
05〜0.50として注入するのか望ましく、目的とす
るフロンの混合比率(通常3〜20%)より大きい割合
で混入する方か効率か良い。As shown in the cross section of FIG. 2, the static mixer 8 has a plurality of ah-shaped elements 9 arranged in a vibrator-like body, which are alternately twisted to the right and twisted in the opposite direction. In this static mixer 8, the PU raw material 4 and the fluorocarbon are rotated and flowed according to the element 9 and mixed. Figure 3 shows the state of this rotational flow.
11 indicates rotation in the right and left elements, respectively, and 11 indicates rotation in two elements. By passing through the static mixer 8, the PtJ raw material 4 and Freon are efficiently mixed and dissolved. The injection pressure of Freon is determined to be the optimum value depending on the viscosity of the PU raw material and the liquid temperature, but it is usually 5 to 1
50 kg/d is desirable, and the mixing ratio of Freon to the PU raw material at this time is 0.5 kg/d.
It is preferable to inject the chlorofluorocarbons at a ratio of 0.05 to 0.50, and it is more efficient to mix in a ratio larger than the target mixing ratio of chlorofluorocarbons (usually 3 to 20%).
PU原料循環戻り配管1には、切換弁15が設けられて
おり、第4図に示すように、フロン混入時にはPU原料
4とフロンとを切換弁15からスタティックミキサー8
を通してタンク3に送り、フロンを混入しない時には切
換弁15から直接タンク3に送るようになっている。ま
た、タンク3内には、モーターにより駆動される攪拌ア
ジテータ−(第2ミキサー)12が装備されており、フ
ロン混入時にはこの攪拌アジテータ−12を作動させる
ことにより、さらに混合、溶解が確実となる。The PU raw material circulation return pipe 1 is provided with a switching valve 15, and as shown in FIG.
The fluid is sent to the tank 3 through the flow control valve 15, and when no fluorocarbon is mixed in, the fluid is sent directly to the tank 3 through the switching valve 15. In addition, the tank 3 is equipped with a stirring agitator (second mixer) 12 driven by a motor, and by operating this stirring agitator 12 when Freon is mixed, further mixing and dissolution can be ensured. .
本発明方法の他の実施例として、上記の実施例の構成に
加え、フロンを射出する発泡剤射出ノズルとして、第5
図に示すような多孔ノズル16、或いは、第6図に示す
ような回転ノズル17を前記PU原料抛環戻り配管1に
挿入してもよい、このような発泡剤射出ノズルを使用す
ることによって、混合効率かさらに向上する。As another embodiment of the method of the present invention, in addition to the configuration of the above embodiment, a fifth blowing agent injection nozzle for injecting fluorocarbon is added.
By using such a blowing agent injection nozzle, a porous nozzle 16 as shown in the figure or a rotating nozzle 17 as shown in FIG. 6 may be inserted into the PU raw material ring return pipe 1. Mixing efficiency is further improved.
(尭明の効果)
以上の説明から明らかな通り、本発明の樹−脂原料への
発泡剤の混入方法は、樹脂原料貯留容器と樹脂原料反1
を出成形装置との間に樹脂原料を循環させるため−の循
環回路のうち、樹脂原料反応射出成形装置から樹脂原料
貯留容器へ樹脂原料が回帰する戻り配管中に発泡剤を射
出し、戻り配管中に配置された第1ミキサーによって樹
脂原料と発泡剤とを1次混合し、この混合原料を樹脂原
料貯留容器内の樹脂原料へ進入させ、この樹脂原料貯留
容器内において第2ミキサーによって2次混合するよう
に構成しなので、発泡剤は前記戻り配管内と樹脂原料貯
留容器内とで2段階に攪拌混合され、発泡剤の気化が抑
制されて樹脂原料に発泡剤を効率良く混合することかで
きる。(Effect of Gyomei) As is clear from the above explanation, the method of mixing the blowing agent into the resin raw material of the present invention is based on the resin raw material storage container and the resin raw material container.
In the circulation circuit for circulating the resin raw material between the resin raw material reaction injection molding device and the resin raw material storage container, the foaming agent is injected into the return pipe where the resin raw material returns from the resin raw material reaction injection molding device to the resin raw material storage container. A resin raw material and a foaming agent are mixed together by a first mixer disposed inside the container, the mixed raw material is introduced into a resin raw material in a resin raw material storage container, and a second mixer is used in this resin raw material storage container to mix the resin raw material and a foaming agent. Since the blowing agent is configured to be mixed, the blowing agent is stirred and mixed in two stages in the return pipe and in the resin raw material storage container, and vaporization of the blowing agent is suppressed to efficiently mix the blowing agent with the resin raw material. can.
第1図は本発明の樹脂原料への発泡剤混入方法を実施す
る装置の構成の一実施例を示す図、第2図(2)はスタ
ティックミキサー(第1ミキサー)の断面図、同ibl
はスタティックミキサーのエレメントを示す図、第3図
はスタティックミキサーにおける原料の回転を示す説明
図、第4図は切換弁の作動による原料の流動を示し、(
a)はフロン混入時、(b)はフロン非混入時を示す説
明図、第5図、第6図は本発明の他の実施例における多
孔ノズル及び回転ノズルをそれぞれ示す斜視図、第7図
は従来のtMk原料への発泡剤混入方法を実施する装置
の構成の一例を示す図である。
1 ・・・PU原料循環戻り配管、
2・・・フロンボンベ、
3・・・タンク(樹脂原料貯留容器)、4 ・・・PU
原料、
8・・・スタティックミキサー(第1ミキサー)、12
・・・攪拌アジテータ−(第2ミキサー)、20・・・
RIM設備(樹脂原料反応射出成形装置)第
図
第
図
第
図
3°タンフ(lit蹟秒舛j′%容%)20:RIM設
S(#n眩糾反忌・射出八形装置)手続補正書(方式)
平成2年8月7日Figure 1 is a diagram showing an example of the configuration of an apparatus for implementing the method of mixing a blowing agent into resin raw materials of the present invention, Figure 2 (2) is a sectional view of a static mixer (first mixer), and Figure 2 (2) is a cross-sectional view of a static mixer (first mixer);
is a diagram showing the elements of the static mixer, FIG. 3 is an explanatory diagram showing the rotation of the raw material in the static mixer, and FIG. 4 is a diagram showing the flow of the raw material due to the operation of the switching valve.
a) is an explanatory diagram showing when fluorocarbons are mixed in, and (b) is an explanatory diagram showing when fluorocarbons are not mixed in. FIGS. 5 and 6 are perspective views showing a multi-hole nozzle and a rotating nozzle, respectively, in other embodiments of the present invention, and FIG. 7 1 is a diagram showing an example of the configuration of an apparatus for carrying out a conventional method of mixing a blowing agent into a tMk raw material. 1...PU raw material circulation return piping, 2...Freon cylinder, 3...tank (resin raw material storage container), 4...PU
Raw materials, 8... Static mixer (first mixer), 12
... Stirring agitator (second mixer), 20...
RIM equipment (resin raw material reaction injection molding equipment) Figure Figure Figure 3° tampf (lit 100% volume%) 20: RIM equipment S (#n dazzling repulsion/injection octavo equipment) procedure correction Letter (method) August 7, 1990
Claims (1)
樹脂原料を循環させるための循環回路のうち、樹脂原料
反応射出成形装置から樹脂原料貯留容器へ樹脂原料が回
帰する戻り配管中に発泡剤を射出し、戻り配管中に配置
された第1ミキサーによって樹脂原料と発泡剤とを1次
混合し、この混合原料を樹脂原料貯留容器内の樹脂原料
へ進入させ、この樹脂原料貯留容器内において第2ミキ
サーによって2次混合するようにしたことを特徴とする
樹脂原料への発泡剤混入方法。Of the circulation circuit for circulating the resin raw material between the resin raw material storage container and the resin raw material reaction injection molding device, a blowing agent is installed in the return pipe where the resin raw material returns from the resin raw material reaction injection molding device to the resin raw material storage container. is injected, the resin raw material and the blowing agent are mixed together by the first mixer disposed in the return pipe, the mixed raw material is introduced into the resin raw material in the resin raw material storage container, and the resin raw material is introduced into the resin raw material storage container. A method for mixing a blowing agent into a resin raw material, characterized in that secondary mixing is performed by a second mixer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11281590A JPH0410914A (en) | 1990-04-27 | 1990-04-27 | Method for mixing foamable agent into resin material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11281590A JPH0410914A (en) | 1990-04-27 | 1990-04-27 | Method for mixing foamable agent into resin material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0410914A true JPH0410914A (en) | 1992-01-16 |
Family
ID=14596227
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11281590A Pending JPH0410914A (en) | 1990-04-27 | 1990-04-27 | Method for mixing foamable agent into resin material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0410914A (en) |
-
1990
- 1990-04-27 JP JP11281590A patent/JPH0410914A/en active Pending
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