JPS625053B2 - - Google Patents
Info
- Publication number
- JPS625053B2 JPS625053B2 JP56141765A JP14176581A JPS625053B2 JP S625053 B2 JPS625053 B2 JP S625053B2 JP 56141765 A JP56141765 A JP 56141765A JP 14176581 A JP14176581 A JP 14176581A JP S625053 B2 JPS625053 B2 JP S625053B2
- Authority
- JP
- Japan
- Prior art keywords
- resin particles
- mold
- dispersion medium
- heated
- blowing agent
- 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
Links
- 239000002245 particle Substances 0.000 claims description 66
- 229920005989 resin Polymers 0.000 claims description 57
- 239000011347 resin Substances 0.000 claims description 57
- 239000002612 dispersion medium Substances 0.000 claims description 28
- 239000004604 Blowing Agent Substances 0.000 claims description 27
- 239000006260 foam Substances 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 15
- 229920003002 synthetic resin Polymers 0.000 claims description 15
- 239000000057 synthetic resin Substances 0.000 claims description 15
- 238000005187 foaming Methods 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 239000002002 slurry Substances 0.000 claims description 10
- 238000009835 boiling Methods 0.000 claims description 9
- 230000004927 fusion Effects 0.000 claims description 7
- 150000002894 organic compounds Chemical class 0.000 claims description 7
- 229920001169 thermoplastic Polymers 0.000 claims description 5
- 239000004416 thermosoftening plastic Substances 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 3
- 238000000034 method Methods 0.000 description 10
- 239000004088 foaming agent Substances 0.000 description 9
- 238000010097 foam moulding Methods 0.000 description 8
- 238000000465 moulding Methods 0.000 description 7
- -1 polyethylene Polymers 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical group C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection 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
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920005672 polyolefin resin 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
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-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
- 238000007796 conventional method Methods 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
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000002666 chemical blowing agent Substances 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
- 238000004891 communication Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000003963 dichloro group Chemical group Cl* 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 229920005674 ethylene-propylene random copolymer Polymers 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 235000011187 glycerol Nutrition 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
- 229920005669 high impact polystyrene Polymers 0.000 description 1
- 239000004797 high-impact polystyrene Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229910001872 inorganic gas Inorganic materials 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-L isophthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC(C([O-])=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-L 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
- 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
- 238000002156 mixing Methods 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 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
- 230000000704 physical effect Effects 0.000 description 1
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001707 polybutylene terephthalate Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 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
- 239000011667 zinc carbonate Substances 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 235000004416 zinc carbonate Nutrition 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
- B29C67/00—Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00
- B29C67/20—Shaping techniques not covered by groups B29C39/00 - B29C65/00, B29C70/00 or B29C73/00 for porous or cellular articles, e.g. of foam plastics, coarse-pored
-
- 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
- B29C44/44—Feeding the material to be shaped into a closed space, i.e. to make articles of definite length in solid form
- B29C44/445—Feeding the material to be shaped into a closed space, i.e. to make articles of definite length in solid form in the form of expandable granules, particles or beads
-
- 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
- B29C44/3415—Heating or cooling
- B29C44/3426—Heating by introducing steam in the mould
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Molding Of Porous Articles (AREA)
Description
【発明の詳細な説明】
本発明は合成樹脂を型内で発泡させると同時に
成形して発泡成形物を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 foam molded product by foaming a synthetic resin in a mold and molding the same at the same time.
ポリスチレン系合成樹脂、ポリオレフイン系合
成樹脂等の型内発泡成形物の製造法としては、粒
状にした原料樹脂に発泡剤を含浸して発泡させ、
得られた粒状発泡体(予備発泡粒子)を型内で加
熱して再発泡させると共に発泡粒子同士を融着さ
せることにより成形物とする方法が、従来普通に
行われてきた。しかしながらこの方法は、樹脂粒
子の発泡が2段階に分けて行われるため、工程数
が多く、また消費するエネルギーも多いという欠
点があつた。更にポリオレフイン系樹脂を原料と
して用いる場合には発泡剤が樹脂粒子及び予備発
泡粒子から散逸し易いため、高倍率の発泡成形物
を得ることは著しく困難であつた。このほか、発
泡剤を混入した合成樹脂の溶融物を型内に注入し
て発泡させ、同時に成形する方法も知られている
が、高発泡成形物を製造することができないばか
りか成形速度が著しく遅いという欠点があつた。 The method for producing in-mold foam molded products such as polystyrene synthetic resins and polyolefin synthetic resins involves impregnating granulated raw material resin with a foaming agent and foaming it.
Conventionally, a method has been commonly used in which the obtained granular foam (pre-expanded particles) is heated in a mold to re-foam and the expanded particles are fused together to form a molded article. However, this method has disadvantages in that the foaming of the resin particles is carried out in two stages, resulting in a large number of steps and a large amount of energy consumption. Furthermore, when a polyolefin resin is used as a raw material, the blowing agent tends to dissipate from the resin particles and pre-expanded particles, making it extremely difficult to obtain a foam molded product with a high magnification. Another known method is to inject a molten synthetic resin mixed with a foaming agent into a mold, foam it, and mold it at the same time, but this method not only does not produce a highly foamed molded product, but also significantly slows down the molding speed. It had the drawback of being slow.
これに対して本発明によれば、原料樹脂の種類
には関係なく高発泡成形物を高能率で製造するこ
とができる。 On the other hand, according to the present invention, a highly foamed molded product can be manufactured with high efficiency regardless of the type of raw material resin.
本発明による発泡成形物の製造法の特徴は、発
泡剤を含有する熱可塑性合成樹脂粒子及び該樹脂
粒子を溶解しない分散媒よりなるスラリー状混合
物を、樹脂粒子が融着も発泡も起こさない温度範
囲及び加圧状態において樹脂粒子の熱変形温度以
上の温度に加熱し、次いで未硬化の樹脂発泡物は
通過させないが分散媒は通過させることができ且
つ低圧の系に連通している分散媒排出孔を有する
成形用型内に注入して瞬間的に樹脂粒子の発泡、
発泡した樹脂粒子同士の融着及び分散媒(一部の
発泡剤を含む)の型外逃散を起こさせ、冷却後、
発泡成形物を型より取り出すことにある。 A feature of the method for manufacturing a foam molded product according to the present invention is that a slurry-like mixture consisting of thermoplastic synthetic resin particles containing a blowing agent and a dispersion medium that does not dissolve the resin particles is heated at a temperature at which the resin particles neither fuse nor foam. The dispersion medium is heated to a temperature above the heat distortion temperature of the resin particles in a range and under pressure, and then the dispersion medium is discharged to a system at low pressure, which does not allow the uncured resin foam to pass through, but allows the dispersion medium to pass through. Instant foaming of resin particles by injection into a mold with holes,
After cooling, the foamed resin particles are fused together and the dispersion medium (including some foaming agents) escapes from the mold.
The purpose is to remove the foamed product from the mold.
ここで上記スラリー状混合物は、熱可塑性合成
樹脂粒子、分散媒及び低沸点有機化合物系発泡剤
の混合物を加圧下に加熱した合成樹脂粒子に発泡
剤を吸収させたもの(処理装置から取り出したり
冷却したりしていない、熱処理後の混合物そのも
の)であつてもよく、この場合は発泡剤含浸工程
までもが発泡・成形工程と一体化され、製造工程
の一層の合理化が達成される。 The above slurry-like mixture is obtained by heating a mixture of thermoplastic synthetic resin particles, a dispersion medium, and a low-boiling organic compound blowing agent under pressure, and then absorbing the blowing agent into the synthetic resin particles (taken out from the processing equipment or cooled). In this case, even the blowing agent impregnation step is integrated with the foaming/molding step, thereby achieving further rationalization of the manufacturing process.
以下本発明による発泡成形物の製造法について
詳述する。 The method for producing a foam molded product according to the present invention will be described in detail below.
原料の熱可塑性合成樹脂としては、ポリスチレ
ン系樹脂(例えばポリスチレン、耐衝撃性ポリス
チレン、スチレンアクリロニトリル共重合体)、
ポリオレフイン系樹脂(例えばポリエチレン、ポ
リプロピレン、エチレン・プロピレン共重合体又
はこれらを架橋させたもの)、ポリアミド(例え
ばナイロン12)、共重合ポリエステル(例えばポ
リエチレンテレフタレート・イソフタレート、ポ
リブチレンテレフタレート・ポリテトラメチレン
グリコールブロツク共重合体)など、発泡成形物
の製造に通常使用される樹脂はもちろん、従来は
高倍率発泡体を形成させることが困難であつた樹
脂も広く使用することができる。これらの樹脂
は、通常平均直径が0.5〜10mm、好ましくは1〜
5mm程度の粒子として発泡剤を含有させることが
望ましい。 The raw thermoplastic synthetic resins include polystyrene resins (e.g. polystyrene, high impact polystyrene, styrene acrylonitrile copolymer),
Polyolefin resins (e.g. polyethylene, polypropylene, ethylene/propylene copolymers or crosslinked products thereof), polyamides (e.g. nylon 12), copolymerized polyesters (e.g. polyethylene terephthalate/isophthalate, polybutylene terephthalate/polytetramethylene glycol) It is possible to use a wide range of resins, such as block copolymers), which are conventionally used in the production of foamed molded products, as well as resins that have hitherto been difficult to form into high-density foamed products. These resins usually have an average diameter of 0.5 to 10 mm, preferably 1 to 10 mm.
It is desirable to contain the blowing agent in the form of particles of about 5 mm.
発泡剤としては従来から使われている低沸点有
機化合物系のもの、化学発泡剤、無機ガス等を、
原料樹脂の種類に応じて適宜選んで用いることが
できるが、特に好ましいのは低沸点有機化合物系
のもの、すなわち原料樹脂を化学的に変質させる
ことなく樹脂粒子に浸透することができる沸点が
−50℃〜110℃程度の有機化合物、例えばプロパ
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、シクロブタン、シクロペンタ
ン、シクロヘキサン等の環状脂肪族炭化水素、ト
リクロロフルオロメタン、ジ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
素などである。 As blowing agents, conventionally used low boiling point organic compounds, chemical blowing agents, inorganic gases, etc.
It can be selected and used as appropriate depending on the type of raw material resin, but particularly preferred are those based on low boiling point organic compounds, that is, those with a boiling point of - - which can penetrate into resin particles without chemically altering the raw material resin. Organic compounds at about 50℃ to 110℃, such as aliphatic hydrocarbons such as propane, butane, pentane, hexane, and heptane, cycloaliphatic hydrocarbons such as cyclobutane, cyclopentane, and cyclohexane, trichlorofluoromethane, dichlorofluoromethane, and dichloro These include halogenated hydrocarbons such as difluoromethane, dicrotetrafluoroethane, methyl chloride, ethyl chloride, and methylene chloride.
樹脂粒子に発泡剤を含有させる方法は任意であ
る。例えば次のような方法により行う。 Any method can be used to incorporate the foaming agent into the resin particles. For example, the following method is used.
a 樹脂粒子又はこれを水等の不活性液体からな
る分散媒に懸濁させたものに低沸点有機化合物
系発泡剤を混合し、加圧下に加熱して発泡剤を
樹脂粒子に吸収させた後、冷却し、樹脂粒子を
分取する。a After mixing a low boiling point organic compound blowing agent with resin particles or a suspension of the same in a dispersion medium consisting of an inert liquid such as water, and heating the resin particles under pressure to absorb the blowing agent into the resin particles. , cool, and separate the resin particles.
b 溶融押出装置内で樹脂に発泡剤を混合したの
ち繊条として押出し、急冷後、細断して発泡剤
を含有する樹脂粒子を得る。b. A foaming agent is mixed with a resin in a melt extrusion device, and then extruded as fibers, rapidly cooled, and then shredded to obtain resin particles containing a foaming agent.
c 樹脂粒子を、低温常圧で、液状の発泡剤と長
時間接触させる。c Resin particles are brought into contact with a liquid blowing agent for a long time at low temperature and normal pressure.
但し、前述のように樹脂粒子、分散媒及び低沸
点有機化合物系発泡剤の混合物を加圧下に加熱し
て発泡剤を合成樹脂粒子に吸収させたものをその
まま発泡成形材料として使用する場合には、他の
発泡剤含有樹脂粒子調製法を採用する余地のない
こと言うまでもない。 However, as mentioned above, when a mixture of resin particles, a dispersion medium, and a low-boiling point organic compound blowing agent is heated under pressure to absorb the blowing agent into the synthetic resin particles, and the mixture is used as a foam molding material as it is, Needless to say, there is no room for adopting other blowing agent-containing resin particle preparation methods.
発泡剤を含有する合成樹脂粒子を分散させる分
散媒は、加熱状態においても樹脂を溶解せず、も
ちろん変質もさせないものでなければならない。
その沸点は200℃以下であることが望ましく、あ
まり高沸点のものは成形物から乾燥により分離す
ることが困難である。水はほとんどすべての樹脂
に使用することのできるすぐれた分散媒である
が、ポリスチレンやポリオレフインの場合は、ほ
かにエチレングリコール、グリセリン等水洗可能
なものも使用することができる。 The dispersion medium in which the synthetic resin particles containing the blowing agent are dispersed must be one that does not dissolve the resin even under heating and, of course, does not change its quality.
It is preferable that the boiling point is 200°C or less; if the boiling point is too high, it will be difficult to separate it from the molded product by drying. Water is an excellent dispersion medium that can be used for almost all resins, but in the case of polystyrene and polyolefin, water-washable solvents such as ethylene glycol and glycerin can also be used.
分散媒は樹脂粒子に対して重量比で約1.5〜5
倍量の範囲で用い、両者から、定量移送に容易
な、均一なスラリーが形成されるようにする。 The weight ratio of the dispersion medium to the resin particles is approximately 1.5 to 5.
Double amounts are used so that both forms a uniform slurry that is easy to transfer quantitatively.
なおこのスラリーには、樹脂粒子が加熱された
ときに融着するのを防止するための分散剤とし
て、分散媒に不溶の無機質微粉末(例えば酸化ア
ルミニウム、酸化チタン、炭酸マグネシウム、炭
酸亜鉛、炭酸カルシウム、塩基性炭酸亜鉛等)、
ポリビニルアルコール、カルボキシメチルセルロ
ース等を少量添加してもよい。 This slurry contains fine inorganic powders (e.g. aluminum oxide, titanium oxide, magnesium carbonate, zinc carbonate, carbonate calcium, basic zinc carbonate, etc.),
A small amount of polyvinyl alcohol, carboxymethyl cellulose, etc. may be added.
上述のようにして得られた樹脂粒子のスラリー
を、密閉容器中で撹拌しながら、該樹脂粒子の熱
変形温度(ASTM―O―648、荷重4.6Kg/cm2)以
上の温度に、但し樹脂粒子同士が融着しない程度
に、加熱する。発泡剤のガス化による樹脂粒子の
発泡を起こさせないために、容器は密閉状態を続
け、必要ならば蒸気圧以上の圧力に加圧する。全
体が均一に目標温度まで加熱されたならば、なる
べく早く次の発泡成形工程に移す。 The slurry of resin particles obtained as described above is heated to a temperature higher than the heat deformation temperature of the resin particles (ASTM-O-648, load 4.6 kg/cm 2 ) while stirring in a closed container. Heat to such an extent that the particles do not fuse together. In order to prevent foaming of the resin particles due to gasification of the foaming agent, the container is kept in a closed state, and if necessary, it is pressurized to a pressure higher than the vapor pressure. Once the whole is uniformly heated to the target temperature, move on to the next foam molding process as soon as possible.
成形用の型としては前述のような分散媒排出孔
を有するものを使用する。分散媒排出孔の形状は
任意であるが、通常は直径0.1〜2.0mm程度の小孔
又は幅0.1〜2.0mm程度のスリツトとし、これを、
発泡成形の際に樹脂粒子が発泡し得る低い圧力に
型内を維持するに七分な数だけ設ける。分散媒排
出孔により型内空間が連通する“低圧の系”は常
圧の大気でよいが、必要に応じて、若干大気圧よ
りも減圧又は加圧された閉鎖系としてもよい。 As a molding mold, one having a dispersion medium discharge hole as described above is used. The shape of the dispersion medium discharge hole is arbitrary, but it is usually a small hole with a diameter of about 0.1 to 2.0 mm or a slit with a width of about 0.1 to 2.0 mm.
Seventh of the number is provided to maintain the inside of the mold at a low pressure that allows the resin particles to foam during foam molding. The "low-pressure system" in which the mold space is communicated through the dispersion medium discharge hole may be the atmosphere at normal pressure, but if necessary, it may be a closed system with a pressure slightly lower or higher than atmospheric pressure.
上述のような型内に、前記加熱・加圧状態の樹
脂粒子スラリーの一定量を、プランジヤー、スク
リユー等を用いて注入すると、樹脂粒子は発泡剤
が気化することにより発泡し(注入機構の構造に
よつては樹脂粒子が型に入る直前から発泡が始ま
るが差支えない)、発泡した樹脂粒子は型内で互
に融着して型どおりに成形される。この間、分散
媒は、その種類及び成形条件により一部気化しな
がら、分散媒排出孔から型外へ排出される。分散
媒と共に、分散媒中にあつた一部の発泡剤、分散
剤等も型外に排出される。なお上記型内発泡成形
に際して蒸気等で熱量を補給し、発泡と融着を助
長してもよい。 When a certain amount of the heated and pressurized resin particle slurry is injected into the above-mentioned mold using a plunger, screw, etc., the resin particles foam as the foaming agent vaporizes (the structure of the injection mechanism (Depending on the mold, foaming may start immediately before the resin particles enter the mold.) The foamed resin particles are fused together in the mold and molded into the mold. During this time, the dispersion medium is discharged out of the mold from the dispersion medium discharge hole while being partially vaporized depending on its type and molding conditions. Along with the dispersion medium, a portion of the blowing agent, dispersant, etc. contained in the dispersion medium is also discharged out of the mold. Note that during the above-mentioned in-mold foam molding, heat may be supplied using steam or the like to promote foaming and fusion.
このあと型を水等で冷却し、発泡体を望ましく
は樹脂の融点よりも20℃以上低い温度迄冷却して
十分固化させてから型外に取り出す。 Thereafter, the mold is cooled with water or the like, and the foam is preferably cooled to a temperature 20° C. or more lower than the melting point of the resin, sufficiently solidified, and then taken out of the mold.
本発明における発泡成形工程は、一定の間隔を
保持して同一方向に移動する一対のベルトと側壁
で形成される断面長方形の空間に前記加熱・加圧
状態の樹脂粒子スラリーを吹き込んで行う連続的
な発泡シートの成形であつてもよい。 The foam molding process in the present invention is a continuous process in which the heated and pressurized resin particle slurry is injected into a space with a rectangular cross section formed by a pair of belts and side walls that move in the same direction at a constant interval. It may also be formed into a foamed sheet.
このように本発明によれば発泡性樹脂粒子を一
旦予備発泡させる工程を経由することなしに一挙
に発泡成形物を得ることができ、特に樹脂粒子、
分散媒及び発泡剤の混合物を加圧下に加熱して発
泡剤を樹脂粒子に吸収させたものをそのまま発泡
成形する方法の場合は発泡剤を含有する樹脂粒子
の製造工程までもが連結された製造法となるか
ら、従来の常法に比べると生産能率が大幅に向上
するのはもちろん、消費エネルギーが著減し、装
置及び付帯設備がが簡略化され、人件費も節減さ
れる。また前述のように従来は高倍率発泡成形が
困難であつたポリオレフイン樹脂の場合にも、発
泡剤が散逸する機会がなくなつたことにより、ポ
リスチレン系樹脂の場合と全く同様に、容易に発
泡成形を行うことができる。 As described above, according to the present invention, a foam molded product can be obtained all at once without going through the step of pre-foaming the expandable resin particles, and in particular, the resin particles,
In the case of a method in which a mixture of a dispersion medium and a blowing agent is heated under pressure to absorb the blowing agent into resin particles and then foam-molded as is, the manufacturing process is linked to the manufacturing process of the resin particles containing the blowing agent. Since it is a method, production efficiency is greatly improved compared to the conventional conventional method, as well as energy consumption is significantly reduced, equipment and auxiliary equipment are simplified, and labor costs are also reduced. In addition, as mentioned above, even in the case of polyolefin resin, which was difficult to perform high-magnification foam molding in the past, because there is no chance for the foaming agent to dissipate, foam molding can be easily performed in the same way as in the case of polystyrene resin. It can be performed.
以下実施例を示して本発明を説明する。なお実
施例中に示した引張強度及び伸度はJIS K6767に
従つて測定した値である。 The present invention will be explained below with reference to Examples. Note that the tensile strength and elongation shown in the examples are values measured according to JIS K6767.
実施例 1
エチレン含有量が3.5重量%のエチレン・プロ
ピレンランダム共重合体(メルトインツクス
1.2、熱変形温度106℃)を1個当りの平均重量が
5mgの粒子とし、この粒子100重量部、水(分散
媒)250重量部及びジクロロジフルオロメタン
(発泡剤)20重量部を密閉容器内に装入し、撹拌
下に加熱して徐々に昇温し、140℃で30分間保持
したのち145℃迄昇温した。この後、容器底部の
排出口の弁を開いて容器内のスラリー状混合物を
容器内圧を利用して成形用型に通じる管路に押出
し、管路の途中に設けたプランジヤー式計量移送
手段により、発泡倍率35倍の発泡成形物を得るの
に必要な計算量のスラリーを型内に注入した。用
いた型は6cm×30cm×30cmの閉鎖空間を有し、且
つ上記閉鎖空間と型周辺の大気とを連通させる幅
0.2mm、長さ10mmのスリツトが150個穿設されてお
り、更に水冷が可能なものである。Example 1 Ethylene-propylene random copolymer with an ethylene content of 3.5% by weight (MeltInx)
1.2, heat deformation temperature: 106°C) with an average weight of 5 mg per particle, 100 parts by weight of these particles, 250 parts by weight of water (dispersion medium), and 20 parts by weight of dichlorodifluoromethane (blowing agent) in a closed container. The mixture was heated under stirring to gradually raise the temperature, held at 140°C for 30 minutes, and then raised to 145°C. After that, the outlet valve at the bottom of the container is opened, and the slurry mixture in the container is pushed out into the pipe leading to the mold using the internal pressure of the container, and a plunger-type metering transfer means provided in the middle of the pipe is used to The calculated amount of slurry necessary to obtain a foam molded product with an expansion ratio of 35 times was injected into the mold. The mold used has a closed space of 6 cm x 30 cm x 30 cm, and a width that allows communication between the closed space and the atmosphere around the mold.
It has 150 slits of 0.2 mm and 10 mm in length, and can be water cooled.
注入1分後に50℃の水を流して型を冷却した
後、発泡成形物を型から取り出して65℃で乾燥し
た。得られた発泡成形物は発泡粒子間の境目も目
立たずよく融着していて表面は平滑であり、引張
強度が5.8Kg/cm2、引張伸度が35%の、良好な物
性のものであつた。 One minute after injection, the mold was cooled by running water at 50°C, and then the foam molded product was taken out of the mold and dried at 65°C. The resulting foamed molded product had good physical properties, with the boundaries between the foamed particles not being noticeable, well fused, and a smooth surface with a tensile strength of 5.8 Kg/cm 2 and a tensile elongation of 35%. It was hot.
比較のため、上記実施例における成形用のスラ
リーを大気中に放出し乾燥して嵩発泡倍率39倍の
予備発泡粒子を得、これを2Kg/cm2(G)の空気
で加圧後、上記実施例で用いたもと同じ大きさの
型を用いて140℃の水蒸気加熱により成形して発
泡倍率35倍の成形物を製造した。得られた成形物
は発泡粒子間の融着が不完全であることが肉眼で
認められ、また表面凹凸が著しいものであつた。
引張強度は3.2Kg/cm2、引張伸度は20%であつ
た。 For comparison, the slurry for molding in the above example was discharged into the atmosphere and dried to obtain pre-expanded particles with a bulk expansion ratio of 39 times, and after pressurizing with air at 2 kg/cm 2 (G), Using a mold of the same size as that used in the example, molding was performed by steam heating at 140°C to produce a molded product with an expansion ratio of 35 times. In the molded product obtained, it was observed with the naked eye that the fusion between the expanded particles was incomplete, and the surface was significantly uneven.
The tensile strength was 3.2 Kg/cm 2 and the tensile elongation was 20%.
実施例 2
ポリエチレン粒子にスチレンモノマーを吸収さ
せたのち重合させて、スチレン重合体の量が粒子
全体の重量の45%であるポリエチレン/ポリスチ
レン混合粒子(平均直径4mm、熱変形温度90℃)
を得、その100重量部に発泡剤(ジクロロジフル
オロメタン)30重量部を加えて50℃で10時間撹拌
後、冷却し、未吸収の発泡剤を分離した。吸収さ
れた発泡剤は17重量部であつた。Example 2 Polyethylene/polystyrene mixed particles (average diameter 4 mm, heat distortion temperature 90°C) are produced by absorbing styrene monomer into polyethylene particles and then polymerizing them, so that the amount of styrene polymer is 45% of the total weight of the particles.
30 parts by weight of a blowing agent (dichlorodifluoromethane) was added to 100 parts by weight of the obtained mixture, and after stirring at 50°C for 10 hours, the mixture was cooled and the unabsorbed blowing agent was separated. The blowing agent absorbed was 17 parts by weight.
得られた発泡剤含有樹脂粒子100重量部、水200
重量部及び酸化アルミニウム微粒子0.5重量部を
密閉容器内に装入し、撹拌下に10℃/minの割合
で115℃迄昇温した。得られた加熱・加圧状態の
スラリー状混合物を実施例1と同様にして発泡倍
率24倍の発泡成形物に成形した。得られた成形物
は発泡粒子間の融着及び表面平滑性が良好で引張
強度は2.9Kg/cm2、引張伸度は18%であつた。 100 parts by weight of the obtained blowing agent-containing resin particles, 200 parts by weight of water
Parts by weight and 0.5 parts by weight of aluminum oxide fine particles were charged into a closed container, and the temperature was raised to 115°C at a rate of 10°C/min while stirring. The obtained heated and pressurized slurry mixture was molded into a foam molded product with a foaming ratio of 24 times in the same manner as in Example 1. The obtained molded product had good fusion between expanded particles and surface smoothness, and had a tensile strength of 2.9 Kg/cm 2 and a tensile elongation of 18%.
比較のため、上記発泡剤吸収処理後の樹脂粒子
を水蒸気で110℃に加熱して嵩発泡倍率26倍に予
備発泡させたものを常法により1.3Kg/cm2の水蒸
気加熱により2次発泡成形して発泡倍率24倍の成
形物を製造した。この成形物は融着不良による発
泡粒子の境界が目立ち、表面凹凸も大きなもので
あつた。引張強度は2.2Kg、引張伸度は12%であ
つた。 For comparison, the resin particles after the blowing agent absorption treatment were pre-foamed to a bulk expansion ratio of 26 times by heating them with steam to 110°C, and then secondary foam molding was performed by heating with steam at 1.3 kg/cm 2 using a conventional method. A molded product with a foaming ratio of 24 times was produced. In this molded product, the boundaries between the expanded particles due to poor fusion were noticeable, and the surface had large irregularities. The tensile strength was 2.2Kg and the tensile elongation was 12%.
Claims (1)
該樹脂粒子を溶解しない分散媒よりなるスラリー
状混合物を、樹脂粒子が融着も発泡も起こさない
温度範囲及び加圧状態において樹脂粒子の熱変形
温度以上の温度に加熱し、未硬化の樹脂発泡物は
通過させないが分散媒は通過させることができ且
つ低圧の系に連通している分散媒排出孔を有する
成形用型内に上記加熱されたスラリー状混合物を
注入して樹脂粒子の発泡、発泡した樹脂粒子同士
の融着及び分散媒の型外逃散を起こさせ、冷却
後、発泡成形物を型より取出すことを特徴とする
合成樹脂発泡成形物の製造法。 2 熱可塑性合成樹脂粒子、該樹脂粒子を溶解し
ない分散媒及び低沸点有機化合物系発泡剤からな
るスラリー状混合物を加圧下に加熱して合成樹脂
粒子に発泡剤を吸収させ、処理後の上記混合物
を、樹脂粒子が融着も発泡も起こさない温度範囲
及び加圧状態において樹脂粒子の熱変形温度以上
に昇温した後、未硬化の樹脂発泡物は通過させな
いが分散媒は通過させることができ且つ低圧の系
に連通している分散媒排出孔を有する成形用型内
に注入して樹脂粒子の発泡、発泡した樹脂粒子同
士の融着及び分散媒の型外逃散を起こさせ、冷却
後、発泡成形物を型より取り出すことを特徴とす
る合成樹脂発泡成形物の製造法。[Claims] 1. A slurry-like mixture consisting of thermoplastic synthetic resin particles containing a blowing agent and a dispersion medium that does not dissolve the resin particles is heated in a temperature range and under pressure that neither fuses nor foams the resin particles. Inside the mold, which is heated to a temperature higher than the thermal deformation temperature of the resin particles, has a dispersion medium discharge hole that does not allow the uncured resin foam to pass through, but allows the dispersion medium to pass through, and is connected to a low-pressure system. The heated slurry mixture is injected into the mold to cause foaming of the resin particles, fusion of the foamed resin particles, and escape of the dispersion medium from the mold, and after cooling, the foam molded product is taken out of the mold. A method for producing synthetic resin foam molded products. 2 A slurry-like mixture consisting of thermoplastic synthetic resin particles, a dispersion medium that does not dissolve the resin particles, and a low-boiling organic compound blowing agent is heated under pressure to cause the synthetic resin particles to absorb the blowing agent, and the above-mentioned mixture after treatment is heated. is heated above the heat deformation temperature of the resin particles in a temperature range where neither fusion nor foaming occurs and under pressure, the uncured resin foam is not allowed to pass through, but the dispersion medium is allowed to pass through. In addition, the resin particles are injected into a mold having a dispersion medium discharge hole communicating with a low-pressure system to cause foaming of the resin particles, fusion of the foamed resin particles, and escape of the dispersion medium from the mold, and after cooling, A method for producing a synthetic resin foam molded product, which comprises removing the foam molded product from a mold.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56141765A JPS5845032A (en) | 1981-09-10 | 1981-09-10 | Manufacture of synthetic resin foamed and molded item |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56141765A JPS5845032A (en) | 1981-09-10 | 1981-09-10 | Manufacture of synthetic resin foamed and molded item |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5845032A JPS5845032A (en) | 1983-03-16 |
JPS625053B2 true JPS625053B2 (en) | 1987-02-03 |
Family
ID=15299652
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56141765A Granted JPS5845032A (en) | 1981-09-10 | 1981-09-10 | Manufacture of synthetic resin foamed and molded item |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5845032A (en) |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS492183A (en) * | 1972-04-20 | 1974-01-10 | ||
JPS561344A (en) * | 1979-06-18 | 1981-01-09 | Nishimu Denshi Kogyo Kk | Controlling method for optimum wet-quantity in wet-type insulator stain measurement |
JPS5825334A (en) * | 1981-08-05 | 1983-02-15 | Japan Styrene Paper Co Ltd | Production of polypropylene resin foam |
-
1981
- 1981-09-10 JP JP56141765A patent/JPS5845032A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS492183A (en) * | 1972-04-20 | 1974-01-10 | ||
JPS561344A (en) * | 1979-06-18 | 1981-01-09 | Nishimu Denshi Kogyo Kk | Controlling method for optimum wet-quantity in wet-type insulator stain measurement |
JPS5825334A (en) * | 1981-08-05 | 1983-02-15 | Japan Styrene Paper Co Ltd | Production of polypropylene resin foam |
Also Published As
Publication number | Publication date |
---|---|
JPS5845032A (en) | 1983-03-16 |
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