JP2007191518A - Foam-molded article of thermoplastic resin particle - Google Patents
Foam-molded article of thermoplastic resin particle Download PDFInfo
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- JP2007191518A JP2007191518A JP2006009019A JP2006009019A JP2007191518A JP 2007191518 A JP2007191518 A JP 2007191518A JP 2006009019 A JP2006009019 A JP 2006009019A JP 2006009019 A JP2006009019 A JP 2006009019A JP 2007191518 A JP2007191518 A JP 2007191518A
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- 239000002245 particle Substances 0.000 title claims abstract description 52
- 229920005992 thermoplastic resin Polymers 0.000 title claims abstract description 47
- 238000005187 foaming Methods 0.000 claims abstract description 8
- 239000006260 foam Substances 0.000 claims description 22
- 239000004088 foaming agent Substances 0.000 claims description 11
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 8
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 claims description 8
- 239000004902 Softening Agent Substances 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 6
- 238000000465 moulding Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 4
- 238000007906 compression Methods 0.000 abstract description 3
- 230000006835 compression Effects 0.000 abstract description 3
- 230000001747 exhibiting effect Effects 0.000 abstract description 2
- 238000000034 method Methods 0.000 description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 13
- 238000009413 insulation Methods 0.000 description 13
- 239000000463 material Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 238000006116 polymerization reaction Methods 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 229920001169 thermoplastic Polymers 0.000 description 6
- 239000003063 flame retardant Substances 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
- 239000004416 thermosoftening plastic Substances 0.000 description 5
- -1 acrylic ester Chemical class 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 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 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- 239000001273 butane Substances 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000010097 foam moulding Methods 0.000 description 3
- 239000011491 glass wool Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000011810 insulating material Substances 0.000 description 3
- 239000011490 mineral wool Substances 0.000 description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 238000010558 suspension polymerization method Methods 0.000 description 2
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 2
- 235000019731 tricalcium phosphate Nutrition 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- HGTUJZTUQFXBIH-UHFFFAOYSA-N (2,3-dimethyl-3-phenylbutan-2-yl)benzene Chemical compound C=1C=CC=CC=1C(C)(C)C(C)(C)C1=CC=CC=C1 HGTUJZTUQFXBIH-UHFFFAOYSA-N 0.000 description 1
- AUTSLLHNWAZVLE-UHFFFAOYSA-N 1,1,2,2,3-pentabromo-3-chlorocyclohexane Chemical compound ClC1(Br)CCCC(Br)(Br)C1(Br)Br AUTSLLHNWAZVLE-UHFFFAOYSA-N 0.000 description 1
- DEIGXXQKDWULML-UHFFFAOYSA-N 1,2,5,6,9,10-hexabromocyclododecane Chemical compound BrC1CCC(Br)C(Br)CCC(Br)C(Br)CCC1Br DEIGXXQKDWULML-UHFFFAOYSA-N 0.000 description 1
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 1
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- VEORPZCZECFIRK-UHFFFAOYSA-N 3,3',5,5'-tetrabromobisphenol A Chemical compound C=1C(Br)=C(O)C(Br)=CC=1C(C)(C)C1=CC(Br)=C(O)C(Br)=C1 VEORPZCZECFIRK-UHFFFAOYSA-N 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 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
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001278 adipic acid derivatives Chemical class 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 230000037237 body shape Effects 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 238000012662 bulk polymerization Methods 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
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 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
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- WDPYDDUVWLUIDM-UHFFFAOYSA-N ethyl carbamate;phenol Chemical compound CCOC(N)=O.OC1=CC=CC=C1 WDPYDDUVWLUIDM-UHFFFAOYSA-N 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 239000004794 expanded polystyrene Substances 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 229940052308 general anesthetics halogenated hydrocarbons Drugs 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000005338 heat storage Methods 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000012774 insulation material Substances 0.000 description 1
- 239000003562 lightweight material Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001502 supplementing effect Effects 0.000 description 1
- 229920001187 thermosetting polymer Polymers 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
- 239000013585 weight reducing agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Abstract
Description
本発明は、高温下における寸法安定性、圧縮強度に優れた熱可塑性樹脂粒子発泡成形体に関する。 The present invention relates to a foamed thermoplastic resin particle article having excellent dimensional stability and compressive strength at high temperatures.
内容物が高温になることがある容器やタンク、配管などの構造物の支持台、屋外で高温に曝されることがある枕木、自動車や建築物などの天井材、床材、壁材などのいわゆる支持体には、高温下で高い圧縮強度を発現する素材が使用され、一般的には成形加工のし易さ、コストの観点から、コンクリート、金属などが広く用いられている。 Supports for structures such as containers, tanks and pipes where the contents can become hot, sleepers that can be exposed to high temperatures outdoors, ceiling materials such as cars and buildings, flooring, wall materials, etc. For the so-called support, a material that exhibits high compressive strength at a high temperature is used. Generally, concrete, metal, and the like are widely used from the viewpoint of ease of forming and cost.
ところが、近年、この様な分野においても、省エネルギー化、軽量化が要求されるようになり、これらの観点から、断熱性・保熱性を備えた軽量な素材が望まれるようになってきている。 However, in recent years, even in such fields, energy saving and weight reduction have been demanded. From these viewpoints, lightweight materials having heat insulating properties and heat retaining properties have been desired.
一般的な断熱素材としては、グラスウール、ロックウール、珪酸カルシウムなどがあげられるが、吸水性が高いために、屋外での使用を想定した用途に対しては、雨水等を吸水することで断熱性能が著しく低下するという欠点があった。さらに、グラスウールやロックウールなどの繊維系断熱材は、単独では自立性が無く、構造体としての強度が得られないため、特許文献1の様な特殊な構造を持った支持装置が必要となる。 Typical heat insulation materials include glass wool, rock wool, calcium silicate, etc., but because of its high water absorption, heat insulation performance can be achieved by absorbing rainwater, etc. for applications that are intended for outdoor use. However, there was a drawback that it was significantly reduced. Furthermore, since fiber-based heat insulating materials such as glass wool and rock wool are not self-supporting and cannot provide strength as a structure, a support device having a special structure as in Patent Document 1 is required. .
これらの欠点を補う素材として、熱硬化性樹脂からなる発泡ウレタン製成形体があげられる。発泡ウレタン製成形体は、グラスウール、ロックウールと比べて成形体強度が高く、広い分野で用いられている。ところが、発泡ウレタン製成形体を上記用途に供するためには、300kg/m3以上の高密度で使用する必要があり、十分な断熱性能を得られない上に、靱性が乏しくなるため取扱が悪いと角部が欠けるという欠点があった。また、遊離する塩素やアミン系触媒によって、接触するステンレス等の金属を腐食させる場合があり、使用期間が長期にわたり、金属と接触した状態で使用されることの多いこの様な分野での部材としては不充分なものであった。このような、腐食を防止するため特許文献2では金属との接触面にバイヤー性フィルムを貼付する方法が、また特許文献3にはノボラック樹脂で改質されたフェノールウレタン発泡断熱材が開示されている。さらには熱可塑性樹脂を材料とするブロー成形品による断熱支持装置が特許文献4に開示されているが、いずれもより高価なものになってしまう。 As a material to compensate for these drawbacks, there is a urethane foam molded body made of a thermosetting resin. The molded product made of urethane foam has higher molded product strength than glass wool and rock wool, and is used in a wide range of fields. However, in order to use the urethane foam molded article for the above-mentioned use, it is necessary to use it at a high density of 300 kg / m 3 or more, and sufficient heat insulation performance cannot be obtained. There was a drawback that the corners were missing. In addition, there are cases where corroded stainless steel and other metals are corroded by free chlorine and amine-based catalysts, and as a member in such fields that are often used in contact with metal over a long period of use. Was insufficient. In order to prevent such corrosion, Patent Document 2 discloses a method of attaching a buyer film to a contact surface with metal, and Patent Document 3 discloses a phenol urethane foam heat insulating material modified with a novolac resin. Yes. Furthermore, although the heat insulation support apparatus by the blow molding goods which use a thermoplastic resin as a material is disclosed by patent document 4, all will become a more expensive thing.
一方、熱可塑性樹脂粒子発泡成形体は、緩衝性能、断熱性能に優れ、利用価値の高い素材として広く認知されている。これらの成形体は熱可塑性樹脂からなる為に、水蒸気等の熱源により容易に発泡ができ、型内発泡成形により特殊な形状に成形加工が可能であり、食品容器、保温材、緩衝材など幅広い分野に使用されている。 On the other hand, the thermoplastic resin particle foam molded article is widely recognized as a material having excellent buffer performance and heat insulation performance and high utility value. Since these molded products are made of thermoplastic resin, they can be easily foamed by a heat source such as water vapor, and can be molded into special shapes by in-mold foam molding. A wide range of food containers, heat insulating materials, cushioning materials, etc. Used in the field.
例えば、熱可塑性樹脂粒子発泡成形体の一つであるスチレン系発泡成形体は、水蒸気等の熱源により容易に成形加工が可能であり、型内発泡成形により用途に応じた形状に成形加工が可能であることから幅広い用途に使用されている。ところが、熱可塑性樹脂発泡体の特性上、高温下での寸法安定性が悪く、積載荷重に対して充分な圧縮強度が得がたい場合があるという欠点があるため、非特許文献1ではその使用温度を高くても80℃以下としている。特許文献5には、重合体を構成する単量体が、αメチルスチレン10〜80重量%、アクリロニトリル5〜50重量%、スチレン、クロルスチレン、パラメチルスチレン、t−ブチルスチレン、アクリル酸エステル、メタクリル酸エステルから選ばれた少なくとも1種の化合物が0〜70重量%である発泡性熱可塑性共重合体粒子から得られる発泡成形体が、100℃で168時間放置した際に優れた寸法安定性を示すことが開示されているが、当該文献に具体的に示されている発泡成形体を構成する発泡性熱可塑性粒子は、例えば、実施例1においては、易揮発性発泡剤を10重量部含んでおり、重合転化率が99.4%であるため残存単量体量が多く、かつトルエンを1.0重量部含んでいるため、高温下では良好な圧縮強度を示さない。
以上のような状況に鑑み、本発明は、断熱性、加工性を有し、かつ高温下において寸法安定性と高い圧縮強度を発現する熱可塑性樹脂粒子発泡成形体を提供することにある。 In view of the above situation, the present invention is to provide a thermoplastic resin particle foamed molded article having heat insulation and workability, and exhibiting dimensional stability and high compressive strength at high temperatures.
上記問題を解決すべく鋭意検討したところ、発泡性熱塑性樹脂粒子が、易揮発性発泡剤2重量%以上5重量%以下を含有し、かつ、有機軟化剤の含有量を0.7重量%以下とすることで、断熱性、高温での寸法安定性と圧縮強度に優れた成形体となりえることを見出し、本発明に至った。 As a result of intensive studies to solve the above problems, the foamable thermoplastic resin particles contain 2% by weight or more and 5% by weight or less of the readily volatile foaming agent, and the content of the organic softening agent is 0.7% by weight or less. As a result, it was found that the molded article can be excellent in heat insulation, dimensional stability at high temperature and compressive strength, and has led to the present invention.
即ち、本発明は、発泡性熱可塑性樹脂粒子から得られる発泡成形体であって、密度が50kg/m3以上250kg/m3以下であり、耐熱性を有し、かつ、80℃での圧縮強度が5kgf/cm2以上である熱可塑性樹脂粒子発泡成形体に関する。 That is, the present invention is a foam-molded article obtained from expandable thermoplastic resin particles, having a density of 50 kg / m 3 or more and 250 kg / m 3 or less, heat resistance, and compression at 80 ° C. The present invention relates to a thermoplastic resin particle foam molded article having a strength of 5 kgf / cm 2 or more.
好ましい実施態様としては、
(1)発泡性熱可塑性樹脂粒子が、易揮発性発泡剤2重量%以上5重量%以下を含有し、発泡性熱可塑性樹脂粒子を可塑化しうる有機軟化剤の含有量が0.7重量%以下である、
(2)発泡性熱可塑性樹脂粒子が、アルファメチルスチレン10重量%以上80重量%以下、アクリロニトリル5重量%以上50重量%以下、更に85重量%以下のスチレン系単量体組成で構成される、
(3)自己消火性を有する、
前記記載の熱可塑性樹脂粒子発泡成形体に関する。
As a preferred embodiment,
(1) The foamable thermoplastic resin particles contain 2% by weight or more and 5% by weight or less of the easily volatile foaming agent, and the content of the organic softening agent capable of plasticizing the foamable thermoplastic resin particles is 0.7% by weight. Is
(2) The expandable thermoplastic resin particles are composed of a styrene-based monomer composition of 10% to 80% by weight of alphamethylstyrene, 5% to 50% by weight of acrylonitrile, and further 85% by weight or less.
(3) has self-extinguishing properties,
The present invention relates to the thermoplastic resin particle foam molded article described above.
本発明の第2は、前記記載の熱可塑性樹脂粒子発泡成形体からなる支持体に関する。 2nd of this invention is related with the support body which consists of a thermoplastic resin particle foaming molding of the said description.
本発明の発泡成形体は、耐熱性を有し、かつ80℃での圧縮強度が5kgf/cm2以上である。そのため、従来コンクリート、金属等が用いられてきた容器やタンク、配管などの構造物の支持台、温風の吹き出し口近傍の各種部材、空気調和機の架台、野外で高温に曝される枕木、自動車や建築物などの天井材、床材、壁材などの重量物の支持具、特に温度差の大きい環境にさらされる様な場所に設置されうる支持具に好適に使用することが出来る。 The foamed molded product of the present invention has heat resistance and a compressive strength at 80 ° C. of 5 kgf / cm 2 or more. Therefore, support bases for structures such as containers, tanks, pipes, etc., conventionally used with concrete, metal, etc., various members near the hot air outlet, air conditioner mounts, sleepers exposed to high temperatures outdoors, It can be suitably used as a support for heavy objects such as ceiling materials, floor materials, and wall materials such as automobiles and buildings, particularly for a support that can be installed in a place exposed to an environment with a large temperature difference.
本発明の熱可塑性樹脂粒子発泡成形体(以下、単に発泡成形体と称する場合がある)は、発泡性熱可塑性樹脂粒子から得られる発泡成形体であって、密度が50kg/m3以上250kg/m3以下であり、耐熱性を有し、かつ、80℃での圧縮強度が5kgf/cm2以上である。 The thermoplastic resin particle foam molded article of the present invention (hereinafter sometimes simply referred to as a foam molded article) is a foam molded article obtained from expandable thermoplastic resin particles, and has a density of 50 kg / m 3 or more and 250 kg / m 3 or less, heat resistance, and compressive strength at 80 ° C. is 5 kgf / cm 2 or more.
本発明における耐熱性とは、高温時の寸法安定性を言い、具体的には、80℃で168時間での寸法変化率が±0.5%以内であることを言う。寸法変化率が±0.5%以内であれば、形状保持能力が高い支持具等に好適に使用できる。 The heat resistance in the present invention refers to dimensional stability at a high temperature, and specifically means that the dimensional change rate at 168 hours at 80 ° C. is within ± 0.5%. If the dimensional change rate is within ± 0.5%, it can be suitably used for a support having a high shape retention capability.
本発明における発泡成形体の密度とは、熱可塑性樹脂粒子発泡成形体の見掛け体積当たりの重量で表されるものであって、50kg/m3以上250kg/m3以下である。好ましくは、80kg/m3以上200kg/m3以下、更に好ましくは、80kg/m3以上100kg/m3以下である。当該範囲内で、対象となる荷重によって適宜密度を選択しうる。50kg/m3以上であると、重量物を支えるための強度が得られ、250kg/m3以下であれば優れた断熱性能が発現するため、充分な断熱・保温効果が得られる。 The density of the foamed molded product in the present invention is represented by the weight per apparent volume of the thermoplastic resin particle foamed molded product, and is 50 kg / m 3 or more and 250 kg / m 3 or less. Preferably, 80 kg / m 3 or more 200 kg / m 3 or less, still more preferably not more than 80 kg / m 3 or more 100 kg / m 3. Within this range, the density can be appropriately selected depending on the load to be processed. If it is 50 kg / m 3 or more, strength for supporting heavy objects can be obtained, and if it is 250 kg / m 3 or less, excellent heat insulation performance is exhibited, so that sufficient heat insulation and heat retention effects can be obtained.
本発明において80℃での圧縮強度は、成形体を80℃の温度下で1時間以上養生した後に測定した5%歪時の圧縮強度をいい、本発明の熱可塑性樹脂粒子発泡成形体は5kgf/cm2以上であり、好ましくは、5kgf/cm2以上50kgf/cm2以下である。5kgf/cm2以上であれば、重量物を支えるための充分な強度であると言える。 In the present invention, the compressive strength at 80 ° C. refers to the compressive strength at 5% strain measured after curing the molded body at a temperature of 80 ° C. for 1 hour or more. The thermoplastic resin particle foam molded body of the present invention has 5 kgf. / Cm 2 or more, preferably 5 kgf / cm 2 or more and 50 kgf / cm 2 or less. If it is 5 kgf / cm 2 or more, it can be said that the strength is sufficient to support heavy objects.
本発明の発泡性熱可塑性樹脂粒子を構成する熱可塑性樹脂は、特に限定はなく、例えば、ポリスチレンを主成分とする樹脂、ポリプロピレンを主成分とする樹脂、ポリメタクリル酸エステルを主成分とする樹脂、ポリ塩化ビニルを主成分とする樹脂等が挙げられるが、中でも、熱可塑性樹脂を構成する単量体組成が、アルファメチルスチレン10重量%以上80重量%以下、アクリロニトリル5重量%以上50重量%、更に85重量%以下のスチレン系単量体から構成されることが好ましく、さらに好ましくはアルファメチルスチレン10重量%以上50重量%以下、アクリロニトリル5重量%以上35重量%以下、80重量%以下のスチレン系単量体から構成されていることが好ましい。当該範囲内の組成であれば、耐熱性を有する発泡成形体が得られる傾向にある。 The thermoplastic resin constituting the expandable thermoplastic resin particles of the present invention is not particularly limited. For example, a resin mainly composed of polystyrene, a resin mainly composed of polypropylene, and a resin mainly composed of polymethacrylate. And a resin mainly composed of polyvinyl chloride. Among them, the monomer composition constituting the thermoplastic resin is 10% by weight to 80% by weight of alphamethylstyrene, 5% by weight to 50% by weight of acrylonitrile. Further, it is preferably composed of 85% by weight or less of a styrene monomer, more preferably 10% by weight to 50% by weight of alphamethylstyrene, 5% by weight to 35% by weight of acrylonitrile, and 80% by weight or less. It is preferably composed of a styrene monomer. If it is a composition within the said range, it exists in the tendency for the foaming molding which has heat resistance to be obtained.
本発明の発泡性熱可塑性樹脂粒子は、易揮発性発泡剤を発泡性熱可塑性樹脂粒子中2重量%以上5重量%以下含有し、かつ、発泡性熱可塑性樹脂粒子を可塑化しうる有機軟化剤の含有量が発泡性熱可塑性樹脂粒子中0.7重量%以下であることが好ましい。易揮発性発泡剤が2重量%以上であれば発泡に必要な発泡力が得られ、5重量%以下であれば余分な発泡力が残存せず高温下で良好な圧縮強度を示す傾向にある。 The foamable thermoplastic resin particles of the present invention contain an easily volatile foaming agent in the foamable thermoplastic resin particles in an amount of 2% by weight to 5% by weight, and can be used to plasticize the foamable thermoplastic resin particles. Is preferably 0.7% by weight or less in the foamable thermoplastic resin particles. If the easily volatile foaming agent is 2% by weight or more, the foaming force necessary for foaming is obtained, and if it is 5% by weight or less, the excess foaming force does not remain and tends to exhibit good compressive strength at high temperatures. .
本発明における可塑化しうる有機軟化剤としては、例えば、発泡力を補うことを目的に使用されるトルエン、キシレン、エチルベンゼン等の溶剤、または、フタル酸エステル類、アジピン酸エステル類等の可塑剤、あるいは、熱可塑性樹脂粒子を得る際に使用したアルファメチルスチレン、アクリロニトリル、スチレン系単量体等の重合未反応物を言う。有機軟化剤の含有量は0.7重量%以下であれば高温下で良好な圧縮強度を示す傾向にある。 Examples of the organic softening agent that can be plasticized in the present invention include solvents such as toluene, xylene, and ethylbenzene used for the purpose of supplementing foaming power, or plasticizers such as phthalic acid esters and adipic acid esters, Alternatively, it refers to an unreacted polymer such as alpha methyl styrene, acrylonitrile, styrene monomer used to obtain thermoplastic resin particles. If the content of the organic softening agent is 0.7% by weight or less, it tends to exhibit good compressive strength at high temperatures.
有機軟化剤を0.7重量%以下にするための方法としては、重合転化率を上げることによって発泡性熱可塑性粒子中に残存する単量体量を低減させる方法や溶剤や可塑剤の添加量を低減させる等の方法が挙げられる。 Methods for reducing the organic softener to 0.7% by weight or less include a method for reducing the amount of monomer remaining in the foamable thermoplastic particles by increasing the polymerization conversion rate, and the amount of solvent or plasticizer added. The method of reducing this etc. is mentioned.
有機軟化剤は、一般的に知られている分析方法により求めることができ、例えば、樹脂粒子を溶解し、ガス・クロマトグラフィ−(GC)により内部標準物質を基準に求めることができる。 The organic softening agent can be obtained by a generally known analysis method. For example, it can be obtained by dissolving resin particles and using gas chromatography (GC) with reference to an internal standard substance.
本発明における易揮発性発泡剤としては、例えば、プロパン、ブタン、ペン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式脂肪族炭化水素及びトリクロルフルオロメタン、ジクロルフルオロメタン、ジクロルジフルオロメタン、メチルクロライド、ジクロルテトラフルオロエタン、エチルクロライド等のハロゲン化炭化水素があげられ、これらは単独もしくは2種以上を混合して用いることができる。 Examples of the readily volatile foaming agent in the present invention include aliphatic hydrocarbons such as propane, butane and pentane, cyclic aliphatic hydrocarbons such as cyclobutane, cyclopentane and cyclohexane, and trichlorofluoromethane, dichlorofluoromethane, Halogenated hydrocarbons such as chlorodifluoromethane, methyl chloride, dichlorotetrafluoroethane, ethyl chloride and the like can be mentioned, and these can be used alone or in admixture of two or more.
本発明の支持体とは、重量物の下部に敷設され、重量物の全重量あるいは一部を支える構造を有するものであり、具体的には、給湯設備の温水タンクや熱水槽、醗酵槽など内容物が高温になることがある容器、タンクなどの構造物の断熱支持台や床、温水や熱水、蒸気等の配管を支える断熱支持具があげられるが、用いる場所は構造物の下部に限らず、取付金具などの締め付けや地震時の横揺れで荷重が掛かる側壁面および天面にも好適に使用することができる。また、断熱性に優れた発泡成形体であるので、内容物が高温である場合だけではなく、適宜内容物を冷却水やブラインに切り替えて使用する冷暖房兼用の蓄熱槽やタンク、配管などにも好適で、熱エネルギーのロスばかりではなく結露を効果的に防ぐことができる。用いられる形状は平板であっても良いが、特に本発明では通常発泡ポリスチレンで使用される型内成形機で局面や凹凸に合わせた形状の成形体が安価かつ容易に得られるため、接触する部位が曲面や凹凸や溝を有する形状の場合には利用価値が高い。 The support of the present invention has a structure that is laid under the heavy object and supports the whole weight or a part of the heavy object. Specifically, a hot water tank, a hot water tank, a fermentation tank, etc. Insulation supports and floors for structures such as containers and tanks where the contents can become hot, and insulation supports that support piping for hot water, hot water, steam, etc. can be mentioned, but the place to use is located at the bottom of the structure The present invention is not limited to this, and it can be suitably used for a side wall surface and a top surface on which a load is applied due to tightening of a mounting bracket or the like and a roll in an earthquake. In addition, since it is a foamed molded article with excellent heat insulation properties, not only when the contents are hot, but also in heat storage tanks, tanks, pipes, etc. that are also used for heating and cooling by appropriately switching the contents to cooling water or brine It is suitable and can effectively prevent condensation as well as loss of thermal energy. The shape used may be a flat plate, but in particular, in the present invention, a molded body having a shape matched to the situation and irregularities can be obtained inexpensively and easily on an in-mold molding machine usually used with expanded polystyrene, In the case of a shape having a curved surface, irregularities or grooves, the utility value is high.
また、直射日光に曝されることで環境温度が高温になる建築物の屋根断熱下地材、屋上断熱下地材として用いた場合、太陽電池パネルや太陽温水器、空調設備の室外機などの重量物を大がかりな補強工事を施すことなく設置することができる。トラックや貨車などの車両の天井、船舶の甲板の下地などにも好適に使用できる。 Also, heavy objects such as solar panels, solar water heaters, and outdoor units of air conditioning equipment when used as roof insulation base materials and roof insulation base materials for buildings that become hot when exposed to direct sunlight. Can be installed without extensive reinforcement work. It can also be suitably used for the ceiling of vehicles such as trucks and freight cars, and for the foundation of ship decks.
この他、温風の吹き出し口近傍など高い温度で使用される各種部材、野外で高温に曝されることがある枕木、空気調和機の架台やドレンパン、建築物など壁材等が例示されるが、これに限定されるものではない。また、その実施形態は、表面を保護するため金属板や箔、樹脂などで覆っても良い。 Other examples include various members used at high temperatures such as in the vicinity of a hot air outlet, sleepers that may be exposed to high temperatures in the outdoors, air conditioner mounts and drain pans, and wall materials such as buildings. However, the present invention is not limited to this. In addition, the embodiment may be covered with a metal plate, foil, resin or the like in order to protect the surface.
本発明の発泡成形体は、組立施工もしくは使用中に火気と接触する可能性がある環境下で使用することがあるため、自己消火性を有することが好ましい。本発明における自己消火性とは、JISA9511:2003燃焼性試験において消炎時間が3秒以内であることを言う。 Since the foamed molded article of the present invention may be used in an environment where there is a possibility of contact with fire during assembly or use, it is preferable to have self-extinguishing properties. The self-extinguishing property in the present invention means that the extinguishing time is within 3 seconds in the JISA9511: 2003 flammability test.
本発明における支持体が自己消火性を有するためには、例えば、難燃剤を使用する方法があげられる。難燃剤としては融点が80℃以上のものが好ましい。このような難燃剤としては、ハロゲン系難燃剤が挙げられ、具体的には、ヘキサブロムシクロドデカン、テトラブロムビスフェノールA及びジアリルエーテル、モノクロルペンタブロムシクロヘキサン等があげられる。このような難燃剤を、発泡性熱可塑性粒子を製造する際に添加しておく等の方法により、発泡成形体に良好な自己消火性を付与することができる。 In order for the support in the present invention to have self-extinguishing properties, for example, a method using a flame retardant can be mentioned. A flame retardant having a melting point of 80 ° C. or higher is preferable. Examples of such flame retardants include halogen-based flame retardants, and specific examples include hexabromocyclododecane, tetrabromobisphenol A and diallyl ether, and monochloropentabromocyclohexane. A good self-extinguishing property can be imparted to the foamed molded article by a method such as adding such a flame retardant when producing foamable thermoplastic particles.
本発明における熱可塑性樹脂粒子発泡成形体とする発泡性熱可塑性樹脂粒子を得る為の方法の一例としては、乳化重合法、塊状重合法などの重合方法により得られた重合物をペレット形状に造粒した後、更に発泡剤含浸を行う方法があげられる。また、懸濁重合法により得た造粒された重合体粒子に発泡剤を含浸する方法などがあげられる。製造方法および発泡剤の含浸方法には特に制約は無いが、プロセスの簡便さから、懸濁重合法が好ましい。 As an example of a method for obtaining expandable thermoplastic resin particles as a thermoplastic resin particle foam molded article in the present invention, a polymer obtained by a polymerization method such as an emulsion polymerization method or a bulk polymerization method is formed into a pellet shape. An example is a method of further impregnating with a foaming agent after granulation. Moreover, the method etc. which impregnate the granulated polymer particle obtained by the suspension polymerization method with a foaming agent are mention | raise | lifted. There are no particular restrictions on the production method and impregnation method of the foaming agent, but the suspension polymerization method is preferred because of the simplicity of the process.
このようにして得られた発泡性熱可塑性樹脂粒子は、必要に応じて所望する密度の予備発泡粒子に発泡し、所望の形状を有する金型内に充填し、加熱融着せしめることで熱可塑性樹脂粒子発泡成形体とする。得られた発泡成形体は、その密度が50kg/m3以上250kg/m3以下の発泡成形体であって、耐熱性を有し、かつ、80℃での圧縮強度が5kgf/cm2以上である。 The foamable thermoplastic resin particles obtained in this way are expanded into pre-expanded particles having a desired density as required, filled into a mold having a desired shape, and heat-fused to obtain thermoplasticity. Let it be a resin particle foam molding. The obtained foamed molded product is a foamed molded product having a density of 50 kg / m 3 or more and 250 kg / m 3 or less, has heat resistance, and has a compressive strength at 80 ° C. of 5 kgf / cm 2 or more. is there.
以下に実施例及び比較例をあげるが、これによって本発明は制限されるものではない。尚、測定評価法のうち、上記に記載した以外の項目については以下の通り実施した。
<耐熱性>
発泡成形体を150×150×20(t)mmに切り出したサンプル片を、JIS K 6767(高温時の寸法安定性:B法)に準拠し、80℃で168時間後の加熱寸法変化率を測定した。また、測定終了後の成形体形状の状態を目視にて観察、評価した。
<80℃での圧縮強度>
発泡成形体を50×50×20(t)mmに切り出したサンプル片を、80℃で1時間保持した後、オートグラフを用いて5%歪時の圧縮強度を測定した。
<自己消火性>
発泡成形体を25×200×10(t)mmに切り出したサンプル片にて、JIS A 9511(燃焼性)に準拠し、炎が消えるまでの時間を測定した。3秒以内に炎が消えて残じんがなく、燃焼限界指示線を越えて燃焼しないものを合格とした。
<高温下での形状保持性>
発泡成形体を50×50×20(t)mmに切り出したサンプル片に、80℃で1kg/cm2の荷重をかけ168時間後の発泡成形体の外観を観察した。
Examples and Comparative Examples are given below, but the present invention is not limited thereby. In the measurement evaluation method, items other than those described above were carried out as follows.
<Heat resistance>
A sample piece obtained by cutting the foamed molded product into 150 × 150 × 20 (t) mm was measured in accordance with JIS K 6767 (dimensional stability at high temperature: method B), and the heating dimensional change rate after 168 hours at 80 ° C. It was measured. Moreover, the state of the molded body shape after the measurement was observed and evaluated visually.
<Compressive strength at 80 ° C>
A sample piece obtained by cutting the foamed molded product into 50 × 50 × 20 (t) mm was held at 80 ° C. for 1 hour, and then the compressive strength at 5% strain was measured using an autograph.
<Self-extinguishing>
A sample piece obtained by cutting the foamed molded product into 25 × 200 × 10 (t) mm was measured in accordance with JIS A 9511 (combustibility) until the flame disappeared. Flames that disappeared within 3 seconds, had no residue, and did not burn beyond the combustion limit indicating line were accepted.
<Shape retention at high temperatures>
A sample piece obtained by cutting the foam molded body into 50 × 50 × 20 (t) mm was applied with a load of 1 kg / cm 2 at 80 ° C., and the appearance of the foam molded body after 168 hours was observed.
(実施例1〜3)
撹拌機を具備した反応器に、純水100重量部、第三リン酸カルシウム0.1重量部、α−オレフィンスルフォン酸ソーダ0.004重量部を入れ、撹拌下、アルファメチルスチレン30重量部、アクリロニトリル20重量部、スチレン50重量部からなる単量体にヘキサブロムシクロドデカン7重量部、2,3−ジメチル−2,3−ジフェニルブタン0.5重量部、ジクミルパ−オキサイド0.5重量部及び重合開始剤を混合してオートクレーブ中に加え、100℃で8時間の重合を行った。次いで、ブタン5重量部を加え、100℃で8時間の発泡剤含浸を行った(アルファメチルスチレン、アクリロニトリル、スチレン単量体の重合未反応物の総量は0.4重量%で、その他の有機軟化剤は検出されなかった)。得られた熱可塑性発泡樹脂粒子を洗浄、脱水した後に、水蒸気で加熱することにより表1に示す密度に予備発泡し、常温下で1日放置し養生乾燥を行った。次いで、得られた熱可塑性樹脂予備発泡粒子を、ダイセン製KR−57成形機を用いて、300×450×20(t)mmサイズの金型にて発泡成形品を得た。得られた熱可塑性樹脂粒子発泡成形体を用いて評価を行い表1に示す結果を得た。
A reactor equipped with a stirrer was charged with 100 parts by weight of pure water, 0.1 part by weight of tribasic calcium phosphate, and 0.004 part by weight of sodium α-olefin sulfonate, and 30 parts by weight of alphamethylstyrene and acrylonitrile 20 with stirring. 6 parts by weight of hexastyrene cyclododecane, 0.5 parts by weight of 2,3-dimethyl-2,3-diphenylbutane, 0.5 parts by weight of dicumyl peroxide and polymerization initiation The agent was mixed and added to the autoclave, and polymerization was carried out at 100 ° C. for 8 hours. Next, 5 parts by weight of butane was added and impregnated with a blowing agent at 100 ° C. for 8 hours (the total amount of unreacted polymerization products of alphamethylstyrene, acrylonitrile and styrene monomer was 0.4% by weight, No softener was detected). The obtained thermoplastic foamed resin particles were washed and dehydrated, and then pre-foamed to the density shown in Table 1 by heating with water vapor, and allowed to stand at room temperature for 1 day for curing and drying. Next, the obtained thermoplastic resin pre-expanded particles were obtained by using a KR-57 molding machine manufactured by Daisen to obtain a foam-molded product with a 300 × 450 × 20 (t) mm size mold. Evaluation was performed using the obtained thermoplastic resin particle foamed molded article, and the results shown in Table 1 were obtained.
(比較例1)
実施例1と同様に熱可塑性樹脂発泡粒子を得た後、同様の操作で表1に示す密度の成形体を得て、評価を行い表1に示す結果を得た。
(Comparative Example 1)
After obtaining the thermoplastic resin expanded particles in the same manner as in Example 1, a molded product having the density shown in Table 1 was obtained by the same operation, and evaluation was performed to obtain the results shown in Table 1.
(比較例2)
攪拌機を具備した反応器に、純水100重量部、第三リン酸カルシウム0.2重量部、α−オレフィンスルフォン酸ソーダ0.004重量部を入れ、攪拌下、スチレン100重量部及び重合開始剤を混合してオートクレーブ中に加え、100℃で4時間の重合を行った。次いで、ブタン5重量部を加え、115℃で3時間の発泡剤含浸を行った(スチレン単量体の重合未反応物の総量は0.4重量%で、その他の有機軟化剤は検出されなかった)。その後、得られた熱可塑性樹脂発泡粒子を、実施例1と同様の操作で処理を行い、表1に示す密度の成形体を得て、評価を行い表1に示す結果を得た。
(Comparative Example 2)
A reactor equipped with a stirrer is charged with 100 parts by weight of pure water, 0.2 part by weight of tribasic calcium phosphate, and 0.004 part by weight of sodium α-olefin sulfonate, and with stirring, 100 parts by weight of styrene and a polymerization initiator are mixed. Then, it was added to the autoclave and polymerized at 100 ° C. for 4 hours. Next, 5 parts by weight of butane was added and impregnated with a foaming agent at 115 ° C. for 3 hours (the total amount of unreacted styrene monomer polymerization was 0.4% by weight, and no other organic softening agents were detected. ) Thereafter, the obtained foamed thermoplastic resin particles were treated in the same manner as in Example 1 to obtain a molded product having the density shown in Table 1, evaluated, and the results shown in Table 1 were obtained.
(比較例3)
特開昭60−206850号公報の実施例2記載と同様にして得られた発泡性熱可塑性重合体粒子を用いて、発泡倍率を表1に示す密度とした成形体を得て、評価を行い表1に示す結果を得た。
(Comparative Example 3)
Using the foamable thermoplastic polymer particles obtained in the same manner as described in Example 2 of JP-A-60-206850, a molded product having the expansion ratio shown in Table 1 was obtained and evaluated. The results shown in Table 1 were obtained.
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WO2010113874A1 (en) | 2009-03-30 | 2010-10-07 | 積水化成品工業株式会社 | Expandable polystyrene resin particles and process for producing same |
US10563056B2 (en) | 2014-09-29 | 2020-02-18 | Kaneka Corporation | Expandable thermoplastic resin particles, thermoplastic pre-expanded particles, and thermoplastic expansion-molded article |
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JP2001131327A (en) * | 1999-11-05 | 2001-05-15 | Kanegafuchi Chem Ind Co Ltd | Molded foam of polypropylene resin composition |
JP2002226622A (en) * | 2001-02-01 | 2002-08-14 | Hitachi Chem Co Ltd | Expandable rubber modified acrylonitrile-styrene resin particle, its manufacturing method and expanded molded article |
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JP2001131327A (en) * | 1999-11-05 | 2001-05-15 | Kanegafuchi Chem Ind Co Ltd | Molded foam of polypropylene resin composition |
JP2002226622A (en) * | 2001-02-01 | 2002-08-14 | Hitachi Chem Co Ltd | Expandable rubber modified acrylonitrile-styrene resin particle, its manufacturing method and expanded molded article |
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