JP2012072279A - Resin pellet for foam molding, method for manufacturing the same and method for manufacturing foamed resin molded article - Google Patents
Resin pellet for foam molding, method for manufacturing the same and method for manufacturing foamed resin molded article Download PDFInfo
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- JP2012072279A JP2012072279A JP2010218040A JP2010218040A JP2012072279A JP 2012072279 A JP2012072279 A JP 2012072279A JP 2010218040 A JP2010218040 A JP 2010218040A JP 2010218040 A JP2010218040 A JP 2010218040A JP 2012072279 A JP2012072279 A JP 2012072279A
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- resin
- foamed
- foam molding
- foaming agent
- chemical foaming
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- 229920005989 resin Polymers 0.000 title claims abstract description 102
- 239000011347 resin Substances 0.000 title claims abstract description 102
- 239000008188 pellet Substances 0.000 title claims abstract description 49
- 238000010097 foam moulding Methods 0.000 title claims abstract description 37
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 18
- 238000000034 method Methods 0.000 title abstract description 9
- 239000000843 powder Substances 0.000 claims abstract description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000011230 binding agent Substances 0.000 claims abstract description 25
- 239000000203 mixture Substances 0.000 claims abstract description 15
- 239000004088 foaming agent Substances 0.000 claims description 49
- 239000000126 substance Substances 0.000 claims description 48
- 238000002844 melting Methods 0.000 claims description 17
- 230000008018 melting Effects 0.000 claims description 17
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 16
- 239000002245 particle Substances 0.000 claims description 16
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 16
- 238000005187 foaming Methods 0.000 claims description 15
- 239000008187 granular material Substances 0.000 claims description 14
- 238000001035 drying Methods 0.000 claims description 4
- 235000012438 extruded product Nutrition 0.000 claims description 3
- 229920006122 polyamide resin Polymers 0.000 abstract description 15
- 238000009834 vaporization Methods 0.000 abstract description 4
- 230000008016 vaporization Effects 0.000 abstract description 4
- 239000006185 dispersion Substances 0.000 abstract description 3
- 238000001125 extrusion Methods 0.000 abstract description 2
- 239000002666 chemical blowing agent Substances 0.000 abstract 3
- 239000000454 talc Substances 0.000 description 10
- 229910052623 talc Inorganic materials 0.000 description 10
- 239000004156 Azodicarbonamide Substances 0.000 description 9
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 9
- 235000019399 azodicarbonamide Nutrition 0.000 description 9
- 238000000465 moulding Methods 0.000 description 8
- 239000004677 Nylon Substances 0.000 description 7
- 229920001778 nylon Polymers 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- -1 polyethylene Polymers 0.000 description 6
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 239000012744 reinforcing agent Substances 0.000 description 3
- 238000005979 thermal decomposition reaction Methods 0.000 description 3
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 2
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004594 Masterbatch (MB) Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000001099 ammonium carbonate Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 239000002216 antistatic agent Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 229920000402 bisphenol A polycarbonate polymer Polymers 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- 239000002667 nucleating agent Substances 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920005668 polycarbonate resin Polymers 0.000 description 2
- 239000004431 polycarbonate resin Substances 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- ASRMWYDEZPXXBA-UHFFFAOYSA-N (sulfonylamino)urea Chemical class NC(=O)NN=S(=O)=O ASRMWYDEZPXXBA-UHFFFAOYSA-N 0.000 description 1
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- MWRWFPQBGSZWNV-UHFFFAOYSA-N Dinitrosopentamethylenetetramine Chemical compound C1N2CN(N=O)CN1CN(N=O)C2 MWRWFPQBGSZWNV-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 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
- 239000002253 acid Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000000805 composite resin Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 239000008202 granule composition Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 150000002832 nitroso derivatives Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000000377 silicon dioxide 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
- 235000011083 sodium citrates Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
本発明は、発泡樹脂成形品の原料となる発泡成形用樹脂ペレット、その製造方法及び発泡樹脂成形品の製造方法に関する。 The present invention relates to a resin pellet for foam molding that is a raw material of a foamed resin molded product, a method for producing the pellet, and a method for producing a foamed resin molded product.
発泡樹脂成形品の製造方法として、発泡樹脂成形品の主成分であるベース樹脂のペレットに化学発泡剤の粉粒体をブレンドして射出成形機に投入する製造方法が知られている(例えば、特許文献1)。 As a method for producing a foamed resin molded product, a production method is known in which a powder of a chemical foaming agent is blended into pellets of a base resin, which is the main component of the foamed resin molded product, and then charged into an injection molding machine (for example, Patent Document 1).
しかしながら、微細な粉粒体である化学発泡剤に対して、ペレットの粒径(1mm以上。一般には、平均粒径1〜5mmのものが多い。)が大きすぎるため、上述した従来の製造方法では、ベース樹脂と化学発泡剤との分散性を高めることが困難であった。このため、発泡倍率のばらつきが発生するという問題があった。 However, since the particle diameter of the pellet (1 mm or more. Generally, the average particle diameter is often 1 to 5 mm) is too large with respect to the chemical foaming agent which is a fine granular material. Therefore, it was difficult to improve the dispersibility between the base resin and the chemical foaming agent. For this reason, there existed a problem that the dispersion | variation in foaming magnification generate | occur | produced.
本発明は、上記事情に鑑みてなされたもので、発泡倍率のばらつきを低減可能な発泡成形用樹脂ペレット、その製造方法及び発泡樹脂成形品の製造方法の提供を目的とする。 This invention is made | formed in view of the said situation, and aims at provision of the resin pellet for foam molding which can reduce the dispersion | variation in foaming ratio, its manufacturing method, and the manufacturing method of a foamed resin molded product.
上記目的を達成するためになされた請求項1の発明に係る発泡成形用樹脂ペレットは、化学発泡剤の粉粒体と、化学発泡剤にて発泡させられる被発泡樹脂の粉粒体とを、水を含んだバインダで結合してなり、水分含有率が5重量%未満であるところに特徴を有する。 In order to achieve the above object, the resin pellet for foam molding according to the invention of claim 1 comprises a powder of a chemical foaming agent and a powder of a foamed resin to be foamed with the chemical foaming agent. It is characterized by being bonded with a water-containing binder and having a moisture content of less than 5% by weight.
請求項2の発明は、請求項1に記載の発泡成形用樹脂ペレットにおいて、被発泡樹脂の融点に代表される溶融開始温度が化学発泡剤の発泡開始温度よりも高いところに特徴を有する。 The invention of claim 2 is characterized in that in the resin pellet for foam molding of claim 1, the melting start temperature typified by the melting point of the resin to be foamed is higher than the foaming start temperature of the chemical foaming agent.
請求項3の発明は、請求項1又は2に記載の発泡成形用樹脂ペレットにおいて、バインダは、水とポリビニルアルコール系樹脂とで構成されたところに特徴を有する。 The invention of claim 3 is characterized in that, in the resin pellet for foam molding of claim 1 or 2, the binder is composed of water and a polyvinyl alcohol resin.
請求項4の発明は、請求項1乃至3の何れか1の請求項に記載の発泡成形用樹脂ペレットにおいて、被発泡樹脂の粉粒体の平均粒径が250〜400μmであり、化学発泡剤の粉粒体の平均粒径が5〜30μmであるところに特徴を有する。 According to a fourth aspect of the present invention, there is provided the foamable resin pellet according to any one of the first to third aspects, wherein the foamed resin powder has an average particle size of 250 to 400 μm and a chemical foaming agent. It has the characteristics in the average particle diameter of 5-30 micrometers.
請求項5の発明に係る発泡樹脂成形品の製造方法は、請求項1乃至4の何れか1の請求項に記載の発泡成形用樹脂ペレットを用いるところに特徴を有する。 The method for producing a foamed resin molded product according to the invention of claim 5 is characterized in that the resin pellet for foam molding according to any one of claims 1 to 4 is used.
請求項6の発明に係る発泡成形用樹脂ペレットの製造方法は、化学発泡剤の粉粒体と、化学発泡剤にて発泡させられる被発泡樹脂の粉粒体とを、水を含んだバインダで結合してなる粉粒体混合物を押出成形し、得られた押出成形体を水分含有率が5重量%未満となるまで乾燥するところに特徴を有する。 According to a sixth aspect of the present invention, there is provided a method for producing a resin pellet for foam molding, comprising a powder containing a chemical foaming agent and a foamed resin powder to be foamed with the chemical foaming agent, in a binder containing water. It is characterized by extruding the combined powder and granule mixture and drying the resulting extrudate until the moisture content is less than 5% by weight.
[被発泡樹脂]
本発明に係る「被発泡樹脂」としては、ポリオレフィン樹脂、ポリアミド樹脂、ポリエステル樹脂、ポリカーボネート樹脂及びABS樹脂などが挙げられる。
[Foamed resin]
Examples of the “foamed resin” according to the present invention include polyolefin resin, polyamide resin, polyester resin, polycarbonate resin, and ABS resin.
ポリオレフィン樹脂としては、ポリエチレン、ポリプロピレン等のホモポリマー、共重合ポリマー又はブレンドポリマーが挙げられる。ポリアミド樹脂としては、6−ナイロン、11−ナイロン、12−ナイロン、46−ナイロン、6,6−ナイロン、6,10−ナイロン、6,12−ナイロン等のホモポリマー、共重合ポリマー又はブレンドポリマーが挙げられる。ポリエステル樹脂としては、芳香族系ポリエステルが好ましく、例えば、ポリエチレンテレフタレート(PET)、ポリブチレンテレフタレート(PBT)、ポリエチレンナフタレート(PEN)等のホモポリマー、共重合ポリマー又はブレンドポリマーである。ポリカーボネート樹脂としては、脂肪族系ポリカーボネート、芳香族系ポリカーボネートの何れであってもよい。具体例としては、ビスフェノールA−ポリカーボネート(BisA−PC)、イソソルバイド−ポリカーボネート等のホモポリマー、共重合ポリマー又はブレンドポリマーが挙げられる。ABS樹脂としては、特に共重合比に制限されることはなく、ブタジエンの比率を低下させた難燃性ABSであってもよい。 Examples of the polyolefin resin include homopolymers such as polyethylene and polypropylene, copolymer polymers, and blend polymers. Examples of polyamide resins include 6-nylon, 11-nylon, 12-nylon, 46-nylon, 6,6-nylon, 6,10-nylon, 6,12-nylon, and other homopolymers, copolymer polymers or blend polymers. Can be mentioned. The polyester resin is preferably an aromatic polyester, for example, a homopolymer such as polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polyethylene naphthalate (PEN), a copolymer or a blend polymer. The polycarbonate resin may be either an aliphatic polycarbonate or an aromatic polycarbonate. Specific examples include homopolymers such as bisphenol A-polycarbonate (BisA-PC) and isosorbide-polycarbonate, copolymer polymers, and blend polymers. The ABS resin is not particularly limited to the copolymerization ratio, and may be flame retardant ABS with a reduced butadiene ratio.
[化学発泡剤]
本発明に係る「化学発泡剤」としては、反応型であっても、熱分解型であってもよいが、好ましくは熱分解型である。また、本発明の効果を阻害しない範囲であれば、これらは単独であっても2種以上を併用してもよい。反応型では、炭酸水素ナトリウムと酸との混合物等の無機系化学発泡剤と、イソシアネート化合物のような有機系化学発泡剤とが挙げられる。熱分解型では、炭酸水素ナトリウム(重曹)、炭酸水素アンモニウム、炭酸アンモニウム、炭酸亜鉛、硝酸ナトリウム、クエン酸ナトリウム等の無機系化学発泡剤と、アゾ化合物、ニトロソ化合物、スルホニルヒドラジド化合物、スルホニルセミカルバジド化合物、トリアゾール化合物等の有機系化学発泡剤とが挙げられる。有機系化学発泡剤としては、具体的には、アゾジカルボンアミド(ADCA)、N,N’−ジニトロソペンタメチレンテトラミン(DPT)、アゾビスイソブチロニトリル(AIBN)等が挙げられる。
[Chemical foaming agent]
The “chemical foaming agent” according to the present invention may be a reactive type or a thermal decomposition type, but is preferably a thermal decomposition type. Moreover, as long as the effect of this invention is not inhibited, these may be individual or may use 2 or more types together. The reactive type includes an inorganic chemical foaming agent such as a mixture of sodium hydrogen carbonate and an acid, and an organic chemical foaming agent such as an isocyanate compound. In the thermal decomposition type, inorganic chemical foaming agents such as sodium hydrogen carbonate (bicarbonate), ammonium hydrogen carbonate, ammonium carbonate, zinc carbonate, sodium nitrate, sodium citrate, azo compounds, nitroso compounds, sulfonyl hydrazide compounds, sulfonyl semicarbazide compounds And organic chemical foaming agents such as triazole compounds. Specific examples of the organic chemical foaming agent include azodicarbonamide (ADCA), N, N′-dinitrosopentamethylenetetramine (DPT), azobisisobutyronitrile (AIBN), and the like.
[バインダ]
本発明に係る「バインダ」は、水と有機系結合剤から構成されたものである。有機系結合剤としては、具体的には、デンプン、ポリビニルアルコール系樹脂が挙げられる。デンプンとしては、米デンプン、馬鈴薯デンプン、コーンスターチ等が挙げられる。ポリビニルアルコール系樹脂としては、完全けん化型ポリビニルアルコール、部分けん化型ポリビニルアルコールの何れであってもよいが、部分けん化型の方が好ましい。
[Binder]
The “binder” according to the present invention is composed of water and an organic binder. Specific examples of the organic binder include starch and polyvinyl alcohol resin. Examples of starch include rice starch, potato starch and corn starch. The polyvinyl alcohol resin may be either fully saponified polyvinyl alcohol or partially saponified polyvinyl alcohol, but the partially saponified type is preferred.
[融点に代表される溶融開始温度]
本発明に係る「融点に代表される溶融開始温度」とは、融点を有する樹脂に関してはその融点、融点を有しない樹脂に関しては、その樹脂がガラス転移してから押出成形が可能な程度に溶融される温度をいう。
[Melting start temperature typified by melting point]
The “melting start temperature typified by the melting point” according to the present invention refers to the melting point of a resin having a melting point and the melting point of a resin having no melting point to the extent that the resin can be extruded after the glass transition. Temperature
[発泡樹脂成形品]
本発明にかかる「発泡樹脂成形品」としては、自動車用部品、調理器具、医療器具等が挙げられる。自動車用部品としては、エンジンカバー、バッテリートレイ、オイルパン、ラジエタートップ、フューズケース、シリンダーヘッドカバー等が挙げられる。
[Foamed resin molded products]
Examples of the “foamed resin molded product” according to the present invention include automotive parts, cooking utensils, medical utensils and the like. Examples of automobile parts include an engine cover, a battery tray, an oil pan, a radiator top, a fuse case, and a cylinder head cover.
[発泡樹脂成形品の製造方法]
発泡樹脂成形品の成形方法としては、コアバック式の発泡成形方法であってもよいし、コアバックを行わずに単に成形金型のキャビティに被発泡樹脂を充填する成形方法であってもよい。また、発泡成形の際に、発泡成形用樹脂ペレットを溶融する装置は、公知の技術であれば特に限定されない。例えば、単軸押出機、2軸押出機、バンバリーミキサー等の溶融混練機がよく用いられる。
[Method for producing foamed resin molded product]
The molding method of the foamed resin molded product may be a core back type foam molding method, or may be a molding method in which the foamed resin is simply filled into the cavity of the molding die without performing the core back. . In addition, an apparatus for melting foam molding resin pellets during foam molding is not particularly limited as long as it is a known technique. For example, a melt kneader such as a single-screw extruder, a twin-screw extruder, or a Banbury mixer is often used.
本発明に係る「発泡成形用樹脂ペレット」には、化学発泡剤以外にも、発泡核剤、強化剤を含有させることができる。発泡核剤としては、例えば、タルク、クレイ、シリカ、炭酸カルシウム、ケイ酸カルシウム等が挙げられる。強化剤としては、ガラス繊維、カーボンブラック、グラファイト、炭酸カルシウム、タルク、マイカ等が挙げられる。 In addition to the chemical foaming agent, the “foam molding resin pellet” according to the present invention can contain a foam nucleating agent and a reinforcing agent. Examples of the foam nucleating agent include talc, clay, silica, calcium carbonate, calcium silicate and the like. Examples of the reinforcing agent include glass fiber, carbon black, graphite, calcium carbonate, talc, mica and the like.
また、本発明に係る「発泡成形用樹脂ペレット」には、必要に応じてさらに、酸化防止剤、帯電防止剤、紫外線防止剤、光安定剤などの各種安定剤、着色剤、滑剤、難燃剤等を含有させることができる。 The “foam molding resin pellet” according to the present invention further includes various stabilizers such as an antioxidant, an antistatic agent, an ultraviolet ray inhibitor, a light stabilizer, a colorant, a lubricant, and a flame retardant as necessary. Etc. can be contained.
本発明では、被発泡樹脂の粉粒体と化学発泡剤の粉粒体とを混合した粉粒体混合物を押出成形することで発泡成形用樹脂ペレットを製造することができる。このように、本発明によれば、樹脂ペレットになる前の比較的小さな粉粒体である被発泡樹脂に化学発泡剤が混合されるので、化学発泡剤と被発泡樹脂との分散性を従来より高めることができる。ここで、本発明に係るバインダは水を含むため、粉粒体混合物を押出成形して得られる押出成形体をそのまま発泡成形用樹脂ペレットとすると、成形金型内でバインダに含まれる水が気化して発泡倍率に誤差が生じてしまう。ところが、本発明では、押出成形体を乾燥して水分含有率を5重量%未満にしたものを発泡成形用樹脂ペレットとして用いたので、水の気化による発泡倍率の誤差を小さくすることができる。このように、本発明では、化学発泡剤と被発泡樹脂との分散性を高めることができ、しかも、水の気化による発泡倍率の誤差を小さくすることができるので、発泡倍率のばらつきを低減することができる。 In the present invention, a resin pellet for foam molding can be produced by extruding a powder mixture obtained by mixing a powdered resin powder and a chemical foaming agent powder. As described above, according to the present invention, since the chemical foaming agent is mixed with the foamed resin that is a relatively small powder before the resin pellets, the dispersibility between the chemical foaming agent and the foamed resin is conventionally improved. Can be increased. Here, since the binder according to the present invention contains water, if the extruded product obtained by extruding the powder mixture is directly used as the resin pellet for foam molding, the water contained in the binder in the molding die is removed. Will cause an error in the expansion ratio. However, in the present invention, since the extrudate is dried and the water content is less than 5% by weight is used as the resin pellet for foam molding, the error of the foaming ratio due to water vaporization can be reduced. As described above, in the present invention, the dispersibility between the chemical foaming agent and the resin to be foamed can be increased, and the error in the foaming ratio due to the vaporization of water can be reduced, thereby reducing the variation in the foaming ratio. be able to.
なお、発泡成形用樹脂ペレットは、発泡成形樹脂品の主原料である主ペレットとして用いてもよいし、主ペレットに混ぜて使用される、所謂、発泡剤マスターバッチペレットとして用いてもよい。 In addition, the resin pellet for foam molding may be used as a main pellet which is a main raw material of the foam molded resin product, or may be used as a so-called foaming agent master batch pellet used by being mixed with the main pellet.
本発明に係る被発泡樹脂は、融点に代表される溶融開始温度が化学発泡剤の発泡開始温度より低くてもよいし、請求項2の発明のように化学発泡剤の発泡開始温度より高くてもよい。なお、請求項2の発明の構成によれば、被発泡樹脂を溶融状態にして化学発泡剤と混練する(コンパウンド)方法によって化学発泡剤と混合することができない場合であっても、樹脂ペレットを製造することができる。 In the resin to be foamed according to the present invention, the melting start temperature represented by the melting point may be lower than the foaming start temperature of the chemical foaming agent, or higher than the foaming start temperature of the chemical foaming agent as in the invention of claim 2. Also good. In addition, according to the structure of invention of Claim 2, even if it is a case where it cannot mix with a chemical foaming agent by the method of knead | mixing with a chemical foaming agent by making a to-be-foamed resin into a molten state (compound), a resin pellet is used. Can be manufactured.
本発明に係るバインダは、上記したように、水とデンプンとから構成されてもよいし、請求項3の発明のように、水とポリビニルアルコール系樹脂とから構成されてもよい。請求項3の発明によれば、デンプン系樹脂を使用した場合に比べて、被発泡樹脂の粉粒体と化学発泡剤の粉粒体との結合を良好に行うことができる。これは、ポリビニルアルコール系樹脂では、デンプンのように過剰に水分を吸収することが抑えられ、乾燥前と乾燥後の水分含有率の差異が低減されるからであると推測される。 The binder according to the present invention may be composed of water and starch as described above, or may be composed of water and a polyvinyl alcohol-based resin as in the third aspect of the invention. According to invention of Claim 3, compared with the case where a starch-type resin is used, the coupling | bonding of the granular material of resin to be foamed and the granular material of a chemical foaming agent can be performed favorably. This is presumably because the polyvinyl alcohol-based resin suppresses excessive moisture absorption like starch and reduces the difference in moisture content before and after drying.
また、被発泡樹脂の粉粒体の平均粒径を250〜400μm、化学発泡剤の粉粒体の平均粒径を5〜30μmとすることで、一般に流通している市販品を使用することができる(請求項4の発明)。 Moreover, it is possible to use a commercially available product in general by setting the average particle size of the foamed resin powder particles to 250 to 400 μm and the average particle size of the chemical foaming agent powder particles to 5 to 30 μm. (Invention of claim 4)
本発明に係る発泡成形用樹脂ペレットは、平均粒径が1〜3mmになっていて、従来の樹脂ペレットの平均粒径(1〜5mm)とほぼ同じ大きさになっている。発泡成形用樹脂ペレットは、「被発泡樹脂」としてのポリアミド樹脂の粉粒体と、化学発泡剤の粉粒体と、タルクの粉粒体とが、水を含んだバインダで結合されてなり、水分含有率が0.2重量%になっている。バインダは、ポリビニルアルコール樹脂(以下、PVAという)と水とで構成されている。そして、水分を除いた残りの99.8重量%分が、ポリアミド樹脂:化学発泡剤:タルク:PVA=72.18/0.27/17.55/10の重量比で配合されている。なお、PVAは、部分けん化型のものが使用されている。 The resin pellet for foam molding according to the present invention has an average particle size of 1 to 3 mm, which is almost the same as the average particle size (1 to 5 mm) of the conventional resin pellet. The resin pellet for foam molding is composed of a polyamide resin powder, a chemical foaming agent, and a talc powder combined as a “foamed resin” with a binder containing water, The water content is 0.2% by weight. The binder is composed of a polyvinyl alcohol resin (hereinafter referred to as PVA) and water. The remaining 99.8% by weight excluding moisture is blended in a weight ratio of polyamide resin: chemical foaming agent: talc: PVA = 72.18 / 0.27 / 17.55 / 10. In addition, the partial saponification type | mold is used for PVA.
なお、化学発泡剤としては、アゾジカルボンアミド(以下、ADCAという)を使用し、その発泡開始温度は180〜210℃であって、ポリアミド樹脂の融点の220℃より低くなっている。 As the chemical foaming agent, azodicarbonamide (hereinafter referred to as ADCA) is used, and the foaming start temperature is 180 to 210 ° C., which is lower than the melting point of the polyamide resin, 220 ° C.
発泡成形用樹脂ペレットは以下のようにして製造される。まず、平均の粉粒体径が250〜400μmのポリアミド樹脂の粉粒体と、平均の粉粒体径が5〜30μmのADCAの粉粒体と、平均の粒径が5.5μmのタルクの粉粒体とを72.18/0.27/17.55の重量比で取り、これら粉粒体を、水を含んだバインダとともに混練し、粘性を有する粉粒体混合物を得る。バインダは、ポリアミド樹脂、ADCA、タルクの総重量を90としたときに、PVAと水の重量が10/35となるように調整されている。 The resin pellet for foam molding is manufactured as follows. First, polyamide resin granules having an average particle diameter of 250 to 400 μm, ADCA granules having an average particle diameter of 5 to 30 μm, and talc having an average particle diameter of 5.5 μm The granular material is taken at a weight ratio of 72.18 / 0.27 / 17.55, and these granular materials are kneaded with a binder containing water to obtain a viscous granular material mixture. The binder is adjusted so that the weight of PVA and water is 10/35 when the total weight of polyamide resin, ADCA and talc is 90.
次いで、粉粒体混合物を、例えば、多数の円形孔を有するプレートの一方側から加圧して線状に押出成形すると共に1〜3mmの長さに切断する。そして、得られた成形体を80℃下で4時間乾燥することで成形体の水分含有率を0.2重量%まで減少させ、発泡成形用樹脂ペレットを得る。 Next, the powder mixture is, for example, pressed from one side of a plate having a large number of circular holes, extruded into a linear shape, and cut into a length of 1 to 3 mm. And the moisture content of a molded object is reduced to 0.2 weight% by drying the obtained molded object at 80 degreeC for 4 hours, and the resin pellet for foam molding is obtained.
次に、本発明に係る「発泡樹脂成形品」としてのエンジンカバーを、上述した発泡成形用樹脂ペレットを用いて製造する方法について説明する。そのためには、まず、コアバック型射出発泡成形機のシリンダに発泡成形用樹脂ペレットを投入する。なお、このとき、必要に応じて発泡成形用樹脂ペレットを予め乾燥しておく。次いで、シリンダ内でポリアミド樹脂を融点(220℃)以上に加熱して溶融状態とし、その溶融状態のポリアミド樹脂にタルク、化学発泡剤(ADCA)を混練して分散させる。このとき、化学発泡剤が発泡開始温度(180〜210℃)以上に加熱されて発泡が開始する。 Next, a method for manufacturing an engine cover as a “foamed resin molded product” according to the present invention using the above-described foamed resin pellets will be described. For this purpose, first, foam molding resin pellets are put into a cylinder of a core back type injection foam molding machine. At this time, the foamed resin pellets are dried in advance if necessary. Next, the polyamide resin is heated to a melting point (220 ° C.) or higher in the cylinder to be in a molten state, and talc and a chemical foaming agent (ADCA) are kneaded and dispersed in the molten polyamide resin. At this time, the chemical foaming agent is heated to the foaming start temperature (180 to 210 ° C.) or higher and foaming starts.
次いで、シリンダ内における溶融状態のポリアミド樹脂を成形金型内に充填する。そして、成形金型の可動型をコアバックさせて溶融状態のポリアミド樹脂を発泡成形する。次いで、成形金型内のポリアミド樹脂を冷却し、可動型を開放することにより、エンジンカバーが取り出される。 Next, the molten polyamide resin in the cylinder is filled into the molding die. Then, the movable mold of the molding die is core-backed to foam-mold the molten polyamide resin. Next, the polyamide resin in the molding die is cooled, and the movable die is opened to remove the engine cover.
本実施形態では、被発泡樹脂(ポリアミド樹脂)の粉粒体と化学発泡剤(ADCA)の粉粒体とを混合した粉粒体混合物を押出成形することで発泡成形用樹脂ペレットを製造することができる。このように、本実施形態によれば、樹脂ペレットになる前の比較的小さな粉粒体である被発泡樹脂に化学発泡剤が混合されるので、化学発泡剤と被発泡樹脂との分散性を従来より高めることができる。ここで、バインダは水を含むため、粉粒体混合物を押出成形して得られる押出成形体をそのまま発泡成形すると、発泡成形の際に成形金型内で水が気化して発泡倍率に誤差が生じてしまう。ところが、本実施形態では、押出成形体を乾燥して水分含有率を5重量%未満にしたものを発泡成形用樹脂ペレットとして用いたので、水が発泡倍率に与える影響を抑えることができる。このように、本実施形態では、化学発泡剤と被発泡樹脂との分散性を高めることができ、しかも、水の気化による発泡倍率の誤差を小さくすることができるので、発泡倍率のばらつきを低減することができる。 In the present embodiment, a resin pellet for foam molding is manufactured by extrusion molding a powder mixture obtained by mixing a powder of resin to be foamed (polyamide resin) and a powder of chemical foaming agent (ADCA). Can do. Thus, according to this embodiment, since the chemical foaming agent is mixed with the foamed resin that is a relatively small powder before the resin pellets, the dispersibility of the chemical foaming agent and the foamed resin is improved. It can be increased than before. Here, since the binder contains water, if the extruded product obtained by extruding the powder mixture is subjected to foam molding as it is, water is vaporized in the molding die during foam molding, resulting in an error in the expansion ratio. It will occur. However, in this embodiment, since the extrudate was dried and the moisture content was less than 5% by weight was used as the foam molding resin pellet, the influence of water on the foaming ratio can be suppressed. As described above, in this embodiment, the dispersibility between the chemical foaming agent and the resin to be foamed can be increased, and the error in the foaming ratio due to the vaporization of water can be reduced, thereby reducing the variation in the foaming ratio. can do.
[他の実施形態]
本発明は、前記実施形態に限定されるものではなく、例えば、以下に説明するような実施形態も本発明の技術的範囲に含まれ、さらに、下記以外にも要旨を逸脱しない範囲内で種々変更して実施することができる。
[Other Embodiments]
The present invention is not limited to the above-described embodiment. For example, the embodiments described below are also included in the technical scope of the present invention, and various other than the following can be made without departing from the scope of the invention. It can be changed and implemented.
(1)前記実施形態における発泡成形用樹脂ペレットは、被発泡樹脂(ポリアミド樹脂)、化学発泡剤(ADCA)及びタルクがバインダで結合された構成であったが、被発泡樹脂と化学発泡剤のみがバインダで結合された構成であってもよいし、被発泡樹脂、化学発泡剤、タルクに加えてガラス繊維や顔料がバインダで結合された構成であってもよい。 (1) The resin pellet for foam molding in the above embodiment has a configuration in which a foamed resin (polyamide resin), a chemical foaming agent (ADCA), and talc are combined with a binder, but only the foamed resin and the chemical foaming agent are used. In addition to the resin to be foamed, the chemical foaming agent, and the talc, a configuration in which glass fibers and pigments are bonded with a binder may be used.
(2)前記実施形態では、発泡成形用樹脂ペレットのみを射出成形機に投入していたが、発泡成形用樹脂ペレットに加えて、添加剤(例えば、強化剤、酸化防止剤、可塑剤など)の粉粒体、当該添加剤のマスターバッチペレット又は熱可塑性樹脂のペレットを投入してもよい。 (2) In the above-described embodiment, only the foam molding resin pellets are charged into the injection molding machine. However, in addition to the foam molding resin pellets, additives (for example, reinforcing agents, antioxidants, plasticizers, etc.) Or a batch of a master batch of the additive or a pellet of a thermoplastic resin may be added.
(3)被発泡樹脂、化学発泡剤、タルクの総重量に対するバインダの重量は、前記実施形態に限定されるものではなく、バインダを増やして被発泡樹脂、化学発泡剤、タルクの粉粒体同士の結合性を向上させてもよい。 (3) The weight of the binder relative to the total weight of the resin to be foamed, the chemical foaming agent, and talc is not limited to the above embodiment, but the binder is increased to increase the amount of the resin to be foamed, the chemical foaming agent, and the particles of talc. The bondability of may be improved.
(4)また、バインダにおけるポリビニルアルコール(PVA)と水の重量比についても、前記実施形態に限定されるものではなく、PVAの割合を増やしてバインダの結合能を向上させてもよい。 (4) Also, the weight ratio of polyvinyl alcohol (PVA) and water in the binder is not limited to the above embodiment, and the binder binding ability may be improved by increasing the proportion of PVA.
なお、本発明の技術範囲には属さないが、本発明の技術を利用して、化学発泡剤の粉粒体の替わりに、酸化防止剤、帯電防止剤、紫外線防止剤、光安定剤等の各種安定剤の粉粒体又は着色剤の粉粒体を、樹脂の粉粒体に結合させた複合樹脂ペレットを製造してもよい。 Although not belonging to the technical scope of the present invention, using the technology of the present invention, an antioxidant, an antistatic agent, an anti-ultraviolet agent, a light stabilizer, etc. can be used instead of the chemical foaming agent granular material. You may manufacture the composite resin pellet which combined the granular material of various stabilizers, or the granular material of the coloring agent with the granular material of resin.
Claims (6)
水分含有率が5重量%未満であることを特徴とする発泡成形用樹脂ペレット。 The chemical foaming agent powder and the foamed resin powder to be foamed with the chemical foaming agent are combined with a binder containing water,
A resin pellet for foam molding characterized by having a water content of less than 5% by weight.
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JP2001323094A (en) * | 2000-05-12 | 2001-11-20 | Otsuka Chem Co Ltd | Resin composition of foamed body and method for manufacturing foamed body using the same |
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JPS5550031A (en) * | 1978-10-05 | 1980-04-11 | Rhone Poulenc Ind | Masterbatch for light weight polyamide moldings |
JPH07196833A (en) * | 1993-12-28 | 1995-08-01 | Nippon Carbide Ind Co Inc | Granular blowing agent composition and its production |
JPH11279313A (en) * | 1998-03-30 | 1999-10-12 | Otsuka Chem Co Ltd | Resin composition for expansion molding, preparation of this composition and expansion molded body prepared by expansion molding this composition |
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