TWI818736B - Plastic composite material and preparation method thereof - Google Patents
Plastic composite material and preparation method thereof Download PDFInfo
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- TWI818736B TWI818736B TW111135561A TW111135561A TWI818736B TW I818736 B TWI818736 B TW I818736B TW 111135561 A TW111135561 A TW 111135561A TW 111135561 A TW111135561 A TW 111135561A TW I818736 B TWI818736 B TW I818736B
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- synthetic rubber
- composite material
- plastic composite
- plastic
- polystyrene
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- 239000004033 plastic Substances 0.000 title claims abstract description 65
- 229920003023 plastic Polymers 0.000 title claims abstract description 65
- 239000002131 composite material Substances 0.000 title claims abstract description 43
- 238000002360 preparation method Methods 0.000 title abstract description 7
- 239000000463 material Substances 0.000 claims abstract description 44
- 229920003051 synthetic elastomer Polymers 0.000 claims abstract description 44
- 239000005061 synthetic rubber Substances 0.000 claims abstract description 44
- 239000004793 Polystyrene Substances 0.000 claims abstract description 26
- 229920002223 polystyrene Polymers 0.000 claims abstract description 25
- 239000012752 auxiliary agent Substances 0.000 claims abstract description 14
- 238000001746 injection moulding Methods 0.000 claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 5
- 239000003381 stabilizer Substances 0.000 claims description 15
- 239000006096 absorbing agent Substances 0.000 claims description 14
- 239000007822 coupling agent Substances 0.000 claims description 12
- 229920001971 elastomer Polymers 0.000 claims description 9
- 239000004088 foaming agent Substances 0.000 claims description 9
- 239000005060 rubber Substances 0.000 claims description 9
- 239000003017 thermal stabilizer Substances 0.000 claims description 8
- 239000002699 waste material Substances 0.000 claims description 5
- -1 gelling accelerators Substances 0.000 claims description 3
- 239000008187 granular material Substances 0.000 claims description 3
- 239000013502 plastic waste Substances 0.000 claims description 3
- 238000010298 pulverizing process Methods 0.000 claims description 2
- 238000001125 extrusion Methods 0.000 abstract description 5
- 238000005469 granulation Methods 0.000 abstract description 3
- 230000003179 granulation Effects 0.000 abstract description 3
- 238000005303 weighing Methods 0.000 abstract 1
- 239000002023 wood Substances 0.000 description 19
- 239000000843 powder Substances 0.000 description 7
- 229920001587 Wood-plastic composite Polymers 0.000 description 6
- 239000011155 wood-plastic composite Substances 0.000 description 6
- 238000000465 moulding Methods 0.000 description 5
- 239000002994 raw material Substances 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 4
- 238000004064 recycling Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 2
- 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 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 229920002522 Wood fibre Polymers 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- SHLNMHIRQGRGOL-UHFFFAOYSA-N barium zinc Chemical compound [Zn].[Ba] SHLNMHIRQGRGOL-UHFFFAOYSA-N 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- AUZONCFQVSMFAP-UHFFFAOYSA-N disulfiram Chemical compound CCN(CC)C(=S)SSC(=S)N(CC)CC AUZONCFQVSMFAP-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
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- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
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- 229920003048 styrene butadiene rubber Polymers 0.000 description 2
- 239000002025 wood fiber Substances 0.000 description 2
- OWRCNXZUPFZXOS-UHFFFAOYSA-N 1,3-diphenylguanidine Chemical compound C=1C=CC=CC=1NC(=N)NC1=CC=CC=C1 OWRCNXZUPFZXOS-UHFFFAOYSA-N 0.000 description 1
- CQSQUYVFNGIECQ-UHFFFAOYSA-N 1-n,4-n-dimethyl-1-n,4-n-dinitrosobenzene-1,4-dicarboxamide Chemical compound O=NN(C)C(=O)C1=CC=C(C(=O)N(C)N=O)C=C1 CQSQUYVFNGIECQ-UHFFFAOYSA-N 0.000 description 1
- MEZZCSHVIGVWFI-UHFFFAOYSA-N 2,2'-Dihydroxy-4-methoxybenzophenone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1O MEZZCSHVIGVWFI-UHFFFAOYSA-N 0.000 description 1
- MHKLKWCYGIBEQF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)morpholine Chemical compound C1COCCN1SC1=NC2=CC=CC=C2S1 MHKLKWCYGIBEQF-UHFFFAOYSA-N 0.000 description 1
- ICGLPKIVTVWCFT-UHFFFAOYSA-N 4-methylbenzenesulfonohydrazide Chemical compound CC1=CC=C(S(=O)(=O)NN)C=C1 ICGLPKIVTVWCFT-UHFFFAOYSA-N 0.000 description 1
- DBOSBRHMHBENLP-UHFFFAOYSA-N 4-tert-Butylphenyl Salicylate Chemical compound C1=CC(C(C)(C)C)=CC=C1OC(=O)C1=CC=CC=C1O DBOSBRHMHBENLP-UHFFFAOYSA-N 0.000 description 1
- UWSMKYBKUPAEJQ-UHFFFAOYSA-N 5-Chloro-2-(3,5-di-tert-butyl-2-hydroxyphenyl)-2H-benzotriazole Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O UWSMKYBKUPAEJQ-UHFFFAOYSA-N 0.000 description 1
- IUNVCWLKOOCPIT-UHFFFAOYSA-N 6-methylheptylsulfanyl 2-hydroxyacetate Chemical compound CC(C)CCCCCSOC(=O)CO IUNVCWLKOOCPIT-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 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
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 206010051246 Photodermatosis Diseases 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- IHBCFWWEZXPPLG-UHFFFAOYSA-N [Ca].[Zn] Chemical compound [Ca].[Zn] IHBCFWWEZXPPLG-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
- 229940063655 aluminum stearate Drugs 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- VJRITMATACIYAF-UHFFFAOYSA-N benzenesulfonohydrazide Chemical compound NNS(=O)(=O)C1=CC=CC=C1 VJRITMATACIYAF-UHFFFAOYSA-N 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- PZGVVCOOWYSSGB-UHFFFAOYSA-L but-2-enedioate;dioctyltin(2+) Chemical compound CCCCCCCC[Sn]1(CCCCCCCC)OC(=O)C=CC(=O)O1 PZGVVCOOWYSSGB-UHFFFAOYSA-L 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- GWOWVOYJLHSRJJ-UHFFFAOYSA-L cadmium stearate Chemical compound [Cd+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O GWOWVOYJLHSRJJ-UHFFFAOYSA-L 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- ZOUQIAGHKFLHIA-UHFFFAOYSA-L copper;n,n-dimethylcarbamodithioate Chemical compound [Cu+2].CN(C)C([S-])=S.CN(C)C([S-])=S ZOUQIAGHKFLHIA-UHFFFAOYSA-L 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- UQLDLKMNUJERMK-UHFFFAOYSA-L di(octadecanoyloxy)lead Chemical compound [Pb+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O UQLDLKMNUJERMK-UHFFFAOYSA-L 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 1
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- FAMRKDQNMBBFBR-UHFFFAOYSA-N ethyl n-ethoxycarbonyliminocarbamate Chemical compound CCOC(=O)N=NC(=O)OCC FAMRKDQNMBBFBR-UHFFFAOYSA-N 0.000 description 1
- 230000004992 fission Effects 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- OCWMFVJKFWXKNZ-UHFFFAOYSA-L lead(2+);oxygen(2-);sulfate Chemical compound [O-2].[O-2].[O-2].[Pb+2].[Pb+2].[Pb+2].[Pb+2].[O-]S([O-])(=O)=O OCWMFVJKFWXKNZ-UHFFFAOYSA-L 0.000 description 1
- UMKARVFXJJITLN-UHFFFAOYSA-N lead;phosphorous acid Chemical compound [Pb].OP(O)O UMKARVFXJJITLN-UHFFFAOYSA-N 0.000 description 1
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- IUJLOAKJZQBENM-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)-2-methylpropan-2-amine Chemical compound C1=CC=C2SC(SNC(C)(C)C)=NC2=C1 IUJLOAKJZQBENM-UHFFFAOYSA-N 0.000 description 1
- 229940032017 n-oxydiethylene-2-benzothiazole sulfenamide Drugs 0.000 description 1
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- FMJSMJQBSVNSBF-UHFFFAOYSA-N octocrylene Chemical compound C=1C=CC=CC=1C(=C(C#N)C(=O)OCC(CC)CCCC)C1=CC=CC=C1 FMJSMJQBSVNSBF-UHFFFAOYSA-N 0.000 description 1
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- 238000001782 photodegradation Methods 0.000 description 1
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- VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- AQHBWWRHIPVRBT-UHFFFAOYSA-N s-(1,3-thiazol-2-yl)thiohydroxylamine Chemical compound NSC1=NC=CS1 AQHBWWRHIPVRBT-UHFFFAOYSA-N 0.000 description 1
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- 238000003860 storage Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
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- 239000011701 zinc Substances 0.000 description 1
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- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
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- Laminated Bodies (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
Abstract
本發明提供一種塑膠複合材料及其製備方法,該複合材料由以下的重量百分比的各成分所製成:聚苯乙烯30%-85%、合成橡膠15%-55%、乳化合成橡膠3%-45%、輔助劑0.1-10%,其製備方法包括將含有聚苯乙烯、合成橡膠、乳化合成橡膠的回收料及/或下腳料進行粉碎;按照該複合材料的各成分的重量百分比分別稱取該聚苯乙烯30%-85%、該合成橡膠15%-55%、該乳化合成橡膠3%-45%;將稱取的該聚苯乙烯、該合成橡膠、該乳化合成橡膠進行混合,得到混合物料;將該混合物料餵入主料口,並將輔助劑0.1-10%餵入側餵料口,進行造粒,得到顆粒狀的複數個塑膠複合材料。本發明的塑膠複合材料適於應用在射出成形工藝,相較於押出成形省去了後續加工,降低生產成本,提升生產效益。The invention provides a plastic composite material and a preparation method thereof. The composite material is made of the following components by weight: 30%-85% polystyrene, 15%-55% synthetic rubber, and 3%-emulsified synthetic rubber. 45% and auxiliary agent 0.1-10%. The preparation method includes crushing recycled materials and/or scraps containing polystyrene, synthetic rubber, and emulsified synthetic rubber; weighing the composite material according to the weight percentage of each component. Polystyrene 30%-85%, the synthetic rubber 15%-55%, and the emulsified synthetic rubber 3%-45%; mix the weighed polystyrene, the synthetic rubber, and the emulsified synthetic rubber to obtain a mixture material; feed the mixed material into the main material port, and feed 0.1-10% of the auxiliary agent into the side feeding port for granulation to obtain multiple granular plastic composite materials. The plastic composite material of the present invention is suitable for application in the injection molding process. Compared with extrusion molding, it eliminates the need for subsequent processing, reduces production costs, and improves production efficiency.
Description
本發明是涉及複合材料的技術領域,尤其是涉及一種塑膠複合材料及其製備方法。The present invention relates to the technical field of composite materials, and in particular to a plastic composite material and a preparation method thereof.
木塑複合材料(Wood Plastic Composite, WPC)是將塑膠原料粉碎,並將木屑或稻殼等植物/木質纖維的木材原料磨粉,以一定比例進行混合,再以押出成形為板材,再經由後製加工為其他製品。由於木塑複合材料具有木材與塑膠的優點,可以取代原本的實木材料或是塑膠用品,可廣泛應用於建材行業、禮品行業、汽車工業、室內家飾、傢俱工業等。而且採用的原料來源於可回收的塑膠及木料,實現回收再利用,友善生態環境。Wood Plastic Composite (WPC) is made by pulverizing plastic raw materials, grinding wood raw materials such as sawdust or rice husks and other plant/wood fiber materials, mixing them in a certain proportion, and then extruding them into sheets. Processed into other products. Since wood-plastic composite materials have the advantages of wood and plastic, they can replace original solid wood materials or plastic products and can be widely used in the building materials industry, gift industry, automobile industry, interior decoration, furniture industry, etc. Moreover, the raw materials used come from recyclable plastic and wood, realizing recycling and reuse, which is friendly to the ecological environment.
然而,塑膠與木質纖維(木粉)二者極性不同,需藉助偶合劑或膠合劑才能結合二者。作為填充木塑複合材料的木粉是為了使塑木更具有實木的質感,但是添加過多,會增加塑木的吸水率,降低塑木密度,使塑木容易腐壞、破損、斷裂或變形。However, plastic and wood fiber (wood powder) have different polarities, and a coupling agent or glue is required to combine them. The purpose of filling wood powder into wood-plastic composite materials is to make the plastic wood have a more solid wood texture. However, adding too much will increase the water absorption rate of the plastic wood, reduce the density of the plastic wood, and make the plastic wood easily rot, damaged, broken or deformed.
此外,在押出過程中,含有木粉的塑膠原料在高溫熔融時黏性很高,不利於押出生產,而且出模後的製品也不容易成形。若生產過程中加入碳酸鈣,雖然可降低黏性,但會使得塑木變硬變脆,長期使用容易讓塑木產生開裂或爆裂的現象。In addition, during the extrusion process, plastic raw materials containing wood powder have high viscosity when melted at high temperatures, which is not conducive to extrusion production, and the products after being ejected from the mold are not easy to shape. If calcium carbonate is added during the production process, although it can reduce the viscosity, it will make the plastic wood hard and brittle. Long-term use may easily cause the plastic wood to crack or burst.
是以,需要提供一種不需添加木粉成分且適於成形製作的複合材料,尤其是射出成形的塑膠複合材料。Therefore, there is a need to provide a composite material that does not require the addition of wood powder and is suitable for molding and production, especially an injection molded plastic composite material.
鑒於上述,本發明旨在提供一種塑膠複合材料,該複合材料由以下的重量百分比的各成分所製成:聚苯乙烯30%-85%、合成橡膠15%-55%、乳化合成橡膠3%-45%、輔助劑0.1-10%。In view of the above, the present invention aims to provide a plastic composite material, which is made of the following weight percentages of each component: polystyrene 30%-85%, synthetic rubber 15%-55%, emulsified synthetic rubber 3% -45%, auxiliary agent 0.1-10%.
進一步,該輔助劑包括有機安定劑、偶合劑、熱安定劑、膠化促進劑、發泡劑、光吸收劑的至少其中之一或組合。Further, the auxiliary agent includes at least one or a combination of organic stabilizers, coupling agents, thermal stabilizers, gelling accelerators, foaming agents, and light absorbers.
進一步,該有機安定劑的重量百分比為0.1%-10%、該偶合劑的重量百分比為0.1%-5%、該熱安定劑的重量百分比為0.1%-3%、該膠化促進劑的重量百分比為0.1%-10%、該發泡劑的重量百分比為0.1%-3%、該光吸收劑的重量百分比為0.1%-3%。Further, the weight percentage of the organic stabilizer is 0.1%-10%, the weight percentage of the coupling agent is 0.1%-5%, the weight percentage of the thermal stabilizer is 0.1%-3%, and the weight percentage of the gelling accelerator is The weight percentage of the foaming agent is 0.1%-10%, the weight percentage of the foaming agent is 0.1%-3%, and the light absorber weight percentage is 0.1%-3%.
進一步,該聚苯乙烯來源於塑膠廢棄物的回收料或下腳料。Furthermore, the polystyrene comes from recycled materials or scraps of plastic waste.
進一步,該合成橡膠及/或該乳化合成橡膠來源於橡膠廢棄物的回收料或下腳料。Furthermore, the synthetic rubber and/or the emulsified synthetic rubber is derived from recycled materials or scraps of rubber waste.
進一步,該回收料及/或該下腳料具有條狀、塊狀、刨花狀的至少其中之一的形狀。Furthermore, the recycled materials and/or the scraps have at least one shape of strips, blocks, and shavings.
進一步,該光吸收劑為吸收300nm-325nm的紫外光。Further, the light absorber absorbs ultraviolet light of 300nm-325nm.
進一步,該光吸收劑為吸收313nm-318nm的紫外光。Further, the light absorber absorbs ultraviolet light of 313nm-318nm.
本發明還提供一種塑膠複合材料的製作方法,將含有聚苯乙烯、合成橡膠、乳化合成橡膠的回收料及/或下腳料進行粉碎;按照該複合材料的各成分的重量百分比分別稱取該聚苯乙烯30%-85%、該合成橡膠15%-55%、該乳化合成橡膠3%-45%;將稱取的該聚苯乙烯、該合成橡膠、該乳化合成橡膠進行混合,得到混合物料;將該混合物料餵入主料口,並將輔助劑0.1-10%餵入側餵料口,進行造粒,得到顆粒狀的複數個塑膠複合材料。The invention also provides a method for making a plastic composite material. The recycled materials and/or scraps containing polystyrene, synthetic rubber, and emulsified synthetic rubber are crushed; the polystyrene is weighed according to the weight percentage of each component of the composite material. Ethylene 30%-85%, the synthetic rubber 15%-55%, and the emulsified synthetic rubber 3%-45%; mix the weighed polystyrene, the synthetic rubber, and the emulsified synthetic rubber to obtain a mixed material; The mixed material is fed into the main feed port, and 0.1-10% of the auxiliary agent is fed into the side feed port for granulation to obtain a plurality of granular plastic composite materials.
本發明的塑膠複合材料加溫至熔融態時,具有較佳及穩定的流動性,適於對成形要求較高的射出成形工藝。由於容易掌控應用在射出成形時的本發明塑膠複合材料的溫度與壓力等成形條件,使得所製成的塑膠成品良率極高。When heated to a molten state, the plastic composite material of the present invention has better and stable fluidity, and is suitable for injection molding processes that require higher molding requirements. Since it is easy to control the molding conditions such as temperature and pressure of the plastic composite material of the present invention when used in injection molding, the yield rate of the produced plastic products is extremely high.
進一步,本發明的塑膠複合材料適於應用在射出成形,因此相較於押出成形省去了後續加工,降低生產成本,提升生產效益。Furthermore, the plastic composite material of the present invention is suitable for application in injection molding. Therefore, compared with extrusion molding, subsequent processing is omitted, production costs are reduced, and production efficiency is improved.
再者,本發明的塑膠複合材料無需添加木粉,製成的成品不吸水,適於潮濕環境,設置於戶外使用,不會有發霉、長斑或蟲蛀,可長時間使用。此外,由於是塑料製造,年久拆除後,可完全回收再利用,對環境友善;相較於使用合成塑木(WPC),廢棄後難以全部分解,無法回收再利用。Furthermore, the plastic composite material of the present invention does not need to add wood powder, and the finished product does not absorb water and is suitable for humid environments. It can be used outdoors without mold, spots or insects, and can be used for a long time. In addition, because it is made of plastic, it can be completely recycled and reused after being dismantled over time, which is environmentally friendly; compared with the use of synthetic wood plastic (WPC), it is difficult to completely decompose after disposal and cannot be recycled and reused.
以下係藉由特定的具體實施例說明本發明之實施方式,熟習此技藝之人士可由本說明書所揭示之內容輕易地瞭解本發明之優點及功效。本發明亦可藉由其它不同之實施方式加以施行或應用,本說明書中的各項細節亦可基於不同觀點與應用,在不悖離本發明所揭示之精神下賦予不同之修飾與變更。此外,本文所有範圍和值都係包含及可合併的。落在本文中所述的範圍內之任何數值或點,例如任何整數都可以作為最小值或最大值以導出下位範圍等。The following describes the implementation of the present invention through specific embodiments. Those skilled in the art can easily understand the advantages and effects of the present invention from the content disclosed in this specification. The present invention can also be implemented or applied in other different embodiments. Various details in this specification can also be modified and changed based on different viewpoints and applications without departing from the spirit of the present invention. In addition, all ranges and values herein are inclusive and combinable. Any value or point that falls within the range described in this article, such as any integer, can be used as a minimum or maximum value to derive a lower range, etc.
以下配合圖式及元件符號對本發明之實施方式做更詳細的說明,俾使熟習該項技藝者在研讀本說明書後能據以實施。The following is a more detailed description of the embodiments of the present invention with reference to drawings and component symbols, so that those skilled in the art can implement them after reading this specification.
本發明實施例提供一種塑膠複合材料,包括如下的重量百分比的各成分:聚苯乙烯(Polystyrene, PS)30%-85%、合成橡膠(Styrene-Butadiene Rubber, SBR)15%-55%、乳化合成橡膠(emulsion polymerized butadiene styrene rubber, ESBR)3%-45%、輔助劑0.1%-10%。Embodiments of the present invention provide a plastic composite material, including the following weight percentages of each component: polystyrene (Polystyrene, PS) 30%-85%, synthetic rubber (Styrene-Butadiene Rubber, SBR) 15%-55%, emulsified Synthetic rubber (emulsion polymerized butadiene styrene rubber, ESBR) 3%-45%, auxiliary agent 0.1%-10%.
聚苯乙烯為一熱塑性塑膠,作為本發明的塑膠複合材料的成分之一,具有好的透光度、硬度、加工尺寸穩定性、流動性、易加工染色;合成橡膠本身為苯乙烯和丁二烯的共聚物,具有和天然橡膠一樣的彈性;乳化合成橡膠,具有優異的耐磨損性、拉伸強度、撕裂強度、耐老化。Polystyrene is a thermoplastic plastic. As one of the components of the plastic composite material of the present invention, it has good light transmittance, hardness, processing dimensional stability, fluidity, and easy processing and dyeing; the synthetic rubber itself is styrene and butadiene. Copolymer of olefins has the same elasticity as natural rubber; emulsified synthetic rubber has excellent wear resistance, tensile strength, tear strength, and aging resistance.
在本發明的實施例中,塑膠複合材料還包括重量百分比為0.1%-10%輔助劑,其中,輔助劑包括:有機安定劑、偶合劑、熱安定劑、膠化促進劑、發泡劑、光吸收劑的至少其中之一或組合。In the embodiment of the present invention, the plastic composite material also includes 0.1%-10% by weight of auxiliary agents, wherein the auxiliary agents include: organic stabilizers, coupling agents, thermal stabilizers, gelling accelerators, foaming agents, At least one or a combination of light absorbers.
有機安定劑用於防止混合物料在加工、使用或回收過程中發生變色或劣化等變質情形。較佳地,有機安定劑包括但不限於:鈣/鋅粉體安定劑、鋇鋅/鋇鈣鋅粉體安定劑、鋇鋅/鈣鋅液體安定劑、有機錫安定劑、鉛系安定劑、磷系安定劑、受阻酚系安定劑。Organic stabilizers are used to prevent discoloration or deterioration of mixed materials during processing, use or recycling. Preferably, organic stabilizers include but are not limited to: calcium/zinc powder stabilizer, barium zinc/barium calcium zinc powder stabilizer, barium zinc/calcium zinc liquid stabilizer, organic tin stabilizer, lead-based stabilizer, Phosphorus stabilizer, hindered phenol stabilizer.
偶合劑用於增強材料的界面性能,改善黏度及分散度,可作為填充材料,其中, 偶合劑包括但不限於,鉻絡合物偶合劑、矽烷偶合劑、鈦酸酯偶合劑、有機過氧化物偶合劑。Coupling agents are used to enhance the interfacial properties of materials, improve viscosity and dispersion, and can be used as filling materials. Coupling agents include, but are not limited to, chromium complex coupling agents, silane coupling agents, titanate coupling agents, and organic peroxides. physical coupling agent.
熱安定劑用於防止加工時的熱降解及防止製品在長期使用過程中的老化。較佳地,熱安定劑包括但不限於:三鹼式硫酸鉛、二鹼式亞磷酸鉛、硬脂酸鎘、硬脂酸鋇、硬脂酸鎂、硬脂酸鋅、硬脂酸鈣、硬脂酸鋁、硬脂酸鉛、馬來酸二正辛基錫﹑S﹐S'-雙(硫代甘醇酸異辛酯)二正辛基錫、磷系熱安定劑。Thermal stabilizers are used to prevent thermal degradation during processing and prevent aging of products during long-term use. Preferably, heat stabilizers include but are not limited to: tribasic lead sulfate, dibasic lead phosphite, cadmium stearate, barium stearate, magnesium stearate, zinc stearate, calcium stearate, Aluminum stearate, lead stearate, di-n-octyltin maleate, S, S'-bis(isooctyl thioglycolate) di-n-octyltin, phosphorus thermal stabilizer.
膠化促進劑用於加速橡膠中的硫化反應。較佳地,膠化促進劑包括但不限於,1,3-二苯胍、二硫化四乙基秋蘭姆、二甲基二硫代氨基甲酸銅、N-環已基-2-苯駢噻唑次磺醯胺、N,N'-二環己基-2-苯並噻唑次磺醯胺、二硫化四甲基秋蘭姆、N-叔丁基-2-苯並噻唑次黃醯胺、N-氧二乙撐-2-苯駢噻唑次磺醯胺、二硫化二苯並噻唑、2-硫醇基苯駢噻唑、超低分子量聚苯乙烯。Gel accelerators are used to accelerate the vulcanization reaction in rubber. Preferably, gelling accelerators include, but are not limited to, 1,3-diphenylguanidine, tetraethylthiuram disulfide, copper dimethyldithiocarbamate, N-cyclohexyl-2-benzene Thiazole sulfenamide, N,N'-dicyclohexyl-2-benzothiazole sulfenamide, tetramethylthiuram disulfide, N-tert-butyl-2-benzothiazole sulfenamide, N-oxydiethylene-2-benzothiazole sulfenamide, dibenzothiazole disulfide, 2-mercaptobenzothiazole, ultra-low molecular weight polystyrene.
發泡劑用於使塑料產生連續或不連續的微孔。較佳地,發泡劑包括但不限於,偶氮二甲醯胺、2,2'-偶氮二異丁腈、偶氮二甲酸二異丙酯、偶氮二甲酸鋇、偶氮二甲酸二乙酯、偶氮胺基苯、N,N'-二亞硝基五次甲基四胺、N,N'-二甲基-N,N'-二亞硝基對苯二甲醯胺、苯磺醯肼、對甲苯磺醯肼、碳酸氫鈉。Foaming agents are used to create continuous or discontinuous micropores in plastics. Preferably, the foaming agent includes, but is not limited to, azodimethylamide, 2,2'-azobisisobutyronitrile, diisopropyl azodicarboxylate, barium azodicarboxylate, azodicarboxylic acid Diethyl ester, azoaminobenzene, N,N'-dinitrosopentamethyltetramine, N,N'-dimethyl-N,N'-dinitrosoterephthalamide , benzene sulfonyl hydrazine, p-toluene sulfonyl hydrazine, sodium bicarbonate.
光吸收劑用於抑制或減緩塑料因吸收紫外光而導致的光降解或光老化作用,延長塑料製品使用及貯存壽命。較佳地,光吸收劑包括但不限於,2,2'-二羥基-4-甲氧基二苯甲酮、2-(2-羥基-3,5-二叔丁基苯基)-5-氯苯並三唑、水楊酸-4-叔丁基苯酯、2-氰-3,3-二苯基丙烯酸-2-乙基己酯。Light absorbers are used to inhibit or slow down the photodegradation or photoaging of plastics caused by absorbing ultraviolet light, and extend the use and storage life of plastic products. Preferably, light absorbers include, but are not limited to, 2,2'-dihydroxy-4-methoxybenzophenone, 2-(2-hydroxy-3,5-di-tert-butylphenyl)-5 -Chlorobenzotriazole, 4-tert-butylphenyl salicylate, 2-ethylhexyl 2-cyano-3,3-diphenylacrylate.
進一步,本發明實施例提供一種塑膠複合材料的製備流程,如圖1所示,Further, embodiments of the present invention provide a preparation process of plastic composite materials, as shown in Figure 1,
步驟S110,將含有聚苯乙烯、合成橡膠、乳化合成橡膠的回收料及/或下腳料進行粉碎;Step S110, crush the recycled materials and/or scraps containing polystyrene, synthetic rubber, and emulsified synthetic rubber;
步驟S120,按照該複合材料的各成分的重量百分比分別稱取該聚苯乙烯30%-85%、該合成橡膠15%-55%、該乳化合成橡膠3%-45%;Step S120: Weigh 30%-85% of the polystyrene, 15%-55% of the synthetic rubber, and 3%-45% of the emulsified synthetic rubber according to the weight percentage of each component of the composite material;
步驟S130,將稱取的該聚苯乙烯、該合成橡膠、該乳化合成橡膠進行混合,得到混合物料;Step S130, mix the weighed polystyrene, the synthetic rubber, and the emulsified synthetic rubber to obtain a mixed material;
步驟S140,將該混合物料餵入主料口,並將輔助劑0.1-10%餵入側餵料口,進行造粒,得到顆粒狀的複數個塑膠複合材料;以及Step S140, feed the mixed material into the main feed port, and feed 0.1-10% of the auxiliary agent into the side feed port for granulation to obtain a plurality of granular plastic composite materials; and
較佳地,在步驟S110中,聚苯乙烯來源於塑膠廢棄物的回收料或是塑膠加工過程中剩餘的廢料、下腳料;合成橡膠、乳化合成橡膠來源於橡膠廢棄物的回收料或是橡膠加工過程中剩餘的廢料、下腳料。Preferably, in step S110, polystyrene is derived from recycled materials of plastic waste or waste materials and leftovers remaining in the plastic processing process; synthetic rubber and emulsified synthetic rubber are derived from recycled materials of rubber waste or rubber. Waste materials and leftovers left during processing.
在本發明的實施例中,不論是塑膠回收料及/或下腳料,或是橡膠回收料及/或下腳料皆不限於其形狀,亦即,本發明可針對各式形狀,例如條狀、塊狀、刨花狀等形狀的塑膠回收料及/或下腳料,以及橡膠回收料及/或下腳料進行粉碎。In embodiments of the present invention, the shapes of plastic recycled materials and/or scraps, or rubber recycled materials and/or scraps are not limited. That is, the present invention can be applied to various shapes, such as strips and blocks. , shavings and other shapes of plastic recycling materials and/or scraps, as well as rubber recycling materials and/or scraps are crushed.
接著,透過粉碎機將上述回收料及/或下腳料進行粉碎,並將粉碎後的含有聚苯乙烯的回收料或下腳料與其他塑膠進行分離,以及將粉碎後的合成橡膠、乳化合成橡膠的回收料或下腳料與其他橡膠進行分離。如此一來,使用來源於回收料及/或下腳料所混合的混合物料中不會含有非必要的其他塑膠及橡膠種類,使得混合物料中的材質種類單純。Next, crush the above-mentioned recycled materials and/or scraps through a crusher, separate the crushed polystyrene-containing recycled materials or scraps from other plastics, and recycle the crushed synthetic rubber and emulsified synthetic rubber. Materials or scraps are separated from other rubber. In this way, the mixed materials mixed using recycled materials and/or scraps will not contain unnecessary other types of plastics and rubbers, making the material types in the mixed materials simple.
較佳地,在得到混合物料後,在步驟S140中,將含有聚苯乙烯30%-85%、合成橡膠15%-55%、乳化合成橡膠3%-45%的混合物料餵入主料口,接著,將輔助劑0.1-10%餵入側餵料口。具體而言,添加介於0.1%-10%的有機安定劑、介於0.1%-5%的偶合劑、介於0.1%-3%的熱安定劑、介於0.1%-10%的膠化促進劑、介於0.1%-3%的發泡劑、介於0.1%-3%的光吸收劑入側餵料口。Preferably, after obtaining the mixed material, in step S140, feed the mixed material containing 30%-85% polystyrene, 15%-55% synthetic rubber, and 3%-45% emulsified synthetic rubber into the main material port. , then, feed 0.1-10% of the auxiliary agent into the side feeding port. Specifically, add 0.1%-10% organic stabilizer, 0.1%-5% coupling agent, 0.1%-3% thermal stabilizer, and 0.1%-10% gelling agent. The accelerator, the foaming agent between 0.1%-3%, and the light absorber between 0.1%-3% enter the side feeding port.
在本發明的實施例中,使用的光吸收劑為吸收300nm-325nm的紫外光。較佳地,為吸收313nm-318nm的紫外光。使用上述波長範圍的光吸收劑可明顯改善聚苯乙烯在生產過程及使用過程中的裂變。In the embodiment of the present invention, the light absorber used absorbs ultraviolet light between 300 nm and 325 nm. Preferably, it absorbs ultraviolet light of 313nm-318nm. The use of light absorbers in the above wavelength range can significantly improve the fission of polystyrene during the production process and use.
將上述混合物料及上述輔助劑分別送入押出機,經熔融混煉後,由模頭押出。在本發明的實施例中,還包括冷卻定型系統,可將經熔融混煉的物料從模頭中擠出,透過旋轉切刀切出酯粒,酯粒因溫度驟降而冷卻定型。如此一來,獲得顆粒狀的複數個塑膠複合材料。The above-mentioned mixed materials and the above-mentioned auxiliary agents are sent to the extruder respectively, and after melting and mixing, they are extruded from the die. In the embodiment of the present invention, a cooling and shaping system is also included, which can extrude the melted and kneaded material from the die, and cut out the ester granules through a rotating cutter. The ester granules are cooled and shaped due to the sudden drop in temperature. In this way, a plurality of granular plastic composite materials are obtained.
較佳地,還包括篩選機,透過振動方式過濾篩選,以將不同顆粒大小的酯粒做篩選區分,並減少酯粒中多餘粉屑。Preferably, it also includes a screening machine that filters and screens through vibration to screen and distinguish ester particles of different particle sizes and reduce excess dust in the ester particles.
透過上述製備方法,進一步,將該些複數個塑膠複合材料進料到射出成形機,加溫至熔融流動狀,並加壓以將熔融流動狀的該些複數個高分子原料從模頭射出至模具,冷卻成形,製成塑膠成品。Through the above preparation method, further, the plurality of plastic composite materials are fed into the injection molding machine, heated to a molten and flowing state, and pressurized to inject the plurality of polymer raw materials in a molten and flowing state from the die to the injection molding machine. The mold is cooled and formed into finished plastic products.
本發明的塑膠複合材料加溫至熔融態時,具有較佳及穩定的流動性,適於對成形要求較高的射出成形工藝。由於容易掌控應用在射出成形時的本發明塑膠複合材料的溫度與壓力等成形條件,使得所製成的塑膠成品良率極高。When heated to a molten state, the plastic composite material of the present invention has better and stable fluidity, and is suitable for injection molding processes that require higher molding requirements. Since it is easy to control the molding conditions such as temperature and pressure of the plastic composite material of the present invention when used in injection molding, the yield rate of the produced plastic products is extremely high.
進一步,本發明的塑膠複合材料適於應用在射出成形,因此相較於押出成形省去了後續加工,降低生產成本,提升生產效益。Furthermore, the plastic composite material of the present invention is suitable for application in injection molding. Therefore, compared with extrusion molding, subsequent processing is omitted, production costs are reduced, and production efficiency is improved.
再者,本發明的塑膠複合材料無需添加木粉,製成的成品不吸水,適於潮濕環境,設置於戶外使用,不會有發霉、長斑或蟲蛀,可長時間使用。此外,由於是塑料製造,年久拆除後,可完全回收再利用,對環境友善;相較於使用合成塑木(WPC),廢棄後難以全部分解,無法回收再利用。Furthermore, the plastic composite material of the present invention does not need to add wood powder, and the finished product does not absorb water and is suitable for humid environments. It can be used outdoors without mold, spots or insects, and can be used for a long time. In addition, because it is made of plastic, it can be completely recycled and reused after being dismantled over time, which is environmentally friendly; compared with the use of synthetic wood plastic (WPC), it is difficult to completely decompose after disposal and cannot be recycled and reused.
上述實施例僅為例示性說明,而非用於限制本發明。任何熟習此項技藝之人士均可在不違背本發明之精神及範疇下,對上述實施例進行修飾與改變。因此,本發明之權利保護範圍係由本發明所附之申請專利範圍所定義,只要不影響本發明之效果及實施目的,應涵蓋於此公開技術內容中。The above embodiments are only illustrative and not intended to limit the present invention. Anyone skilled in the art can make modifications and changes to the above embodiments without departing from the spirit and scope of the invention. Therefore, the scope of rights protection of the present invention is defined by the scope of the patent application attached to the present invention. As long as it does not affect the effect and implementation purpose of the present invention, it should be covered by this disclosed technical content.
S110:步驟 S120:步驟 S130:步驟 S140:步驟 S110: Steps S120: Steps S130: Steps S140: Steps
圖1為本發明實施例提供的塑膠複合材料的製備流程示意圖。Figure 1 is a schematic diagram of the preparation process of a plastic composite material provided by an embodiment of the present invention.
S110:步驟 S110: Steps
S120:步驟 S120: Steps
S130:步驟 S130: Steps
S140:步驟 S140: Steps
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CN101985527A (en) * | 2010-10-29 | 2011-03-16 | 曾广胜 | Environment-friendly plant fiber wood-plastic composite material and preparation method thereof |
CN104194179A (en) * | 2014-08-23 | 2014-12-10 | 青岛优维奥信息技术有限公司 | Wood-like environment-friendly material formula |
CN107922515A (en) * | 2015-09-01 | 2018-04-17 | 株式会社普利司通 | Styrene butadiene ribber, rubber composition and the tire of emulsion polymerization |
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CN101985527A (en) * | 2010-10-29 | 2011-03-16 | 曾广胜 | Environment-friendly plant fiber wood-plastic composite material and preparation method thereof |
CN104194179A (en) * | 2014-08-23 | 2014-12-10 | 青岛优维奥信息技术有限公司 | Wood-like environment-friendly material formula |
CN107922515A (en) * | 2015-09-01 | 2018-04-17 | 株式会社普利司通 | Styrene butadiene ribber, rubber composition and the tire of emulsion polymerization |
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