Development of New Technology for Chemical Recycling of Waste Plastics Using Polyolefin-derived Hydrogen
| Project/Area Number |
15K00597
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Environmental conscious materials and recycle
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| Research Institution | Muroran Institute of Technology |
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Principal Investigator |
UEMICHI Yoshio 室蘭工業大学, 工学研究科, 教授 (90168659)
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| Co-Investigator(Kenkyū-buntansha) |
神田 康晴 室蘭工業大学, 工学研究科, 准教授 (70447085)
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| Project Period (FY) |
2015-04-01 – 2018-03-31
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| Project Status |
Completed (Fiscal Year 2017)
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| Budget Amount *help |
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2017: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2016: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2015: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
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| Keywords | 廃プラスチック / ケミカルリサイクル / ポリオレフィン / ポリスチレン / ガリウムゼオライト触媒 / ポリオレフィン水素 / 芳香族炭化水素 / コーキング / ガリウムゼオライト / リサイクル / 環境技術 / 触媒 / ゼオライト |
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| Outline of Final Research Achievements |
The catalytic degradation of polyolefin/polystyrene mixtures using gallium-supported H-ZSM-5 catalyst was investigated to develop a new technology for chemical recycling of waste plastics. When the concentration of polystyrene in plastic mixtures was about 20%, great coking suppression of polystyrene on the catalyst surface by polyolefin-derived hydrogen was observed and the conversion of the plastics into aromatics proceeded efficiently. Furthermore, from the results of the model reactions using 1-octene and styrene monomer, it was found that the hydrogenation and hydrocracking of styrene monomer were accelerated, while the coking following the dimerization of styrene monomer was suppressed in the presence of polyolefin-derived hydrogen.
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Report
(4 results)
Research Products
(15 results)
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[Presentation] ポリオレフィンの接触分解2016
Author(s)
加賀慎之介，神田康晴，上道芳夫
Organizer
日本化学会北海道支部2016年夏季研究発表会
Place of Presentation
室蘭工業大学（北海道，室蘭市）
Year and Date
2016-07-23
Related Report
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