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(2023) Chemical Engineering Journal_CO2-mediated thermal treatment of disposable plastic food containers

(2023) Chemical Engineering Journal_CO2-mediated thermal treatment of disposable plastic food containers

 

Jung S., Tsang Y.F., Kwon D., Choi D., Chen W.-H., Kim Y.-H., Moon D.H., Kwon E.E.

 

(Elsevier B.V.) Chemical Engineering Journal ISSN: 13858947 Vol.451 Issue. Article No.138603 DOI: 10.1016/j.cej.2022.138603

 

In accordance with global economic prosperity, the frequencies of food delivery and takeout orders have been increasing. The pandemic life, specifically arising from COVID-19, rapidly expanded the food delivery service. Thus, the massive generation of disposable plastic food containers has become significant environmental problems. Establishing a sustainable disposal platform for plastic packaging waste (PPW) of food delivery containers has intrigued particular interest. To comprise this grand challenge, a reliable thermal disposable platform has been suggested in this study. From the pyrolysis process, a heterogeneous plastic mixture of PPW was converted into syngas and value-added hydrocarbons (HCs). PPW collected from five different restaurants consisted of polypropylene (36.9 wt%), polyethylene (10.5 wt%), polyethylene terephthalate (18.1 wt%), polystyrene (13.5 wt%), polyvinyl chloride (4.2 wt%), and other composites (16.8 wt%). Due to these compositional complexities, pyrolysis of PPW led to formations of a variety of benzene derivatives and aliphatic HCs. Adapting multi-stage pyrolysis, the different chemicals were converted into industrial chemicals (benzene, toluene, styrene, etc.). To selectively convert HCs into syngas (H2 and CO), catalytic pyrolysis was adapted using supported Ni catalyst (5 wt% Ni/SiO2). Over Ni catalyst, H2 was produced as a main product due to C[sbnd]H bond scission of HCs. When CO2 was used as a co-reactant, HCs were further transformed to H2 and CO through the chemical reactions of CO2 with gas phase HCs. CO2-assisted catalytic pyrolysis also retarded catalyst deactivation inhibiting coke deposition on Ni catalyst. © 2022 Elsevier B.V.

 

This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (NRF- 2021R1I1A1A01052241 ). This work was supported by the Environment and Conservation Fund of the Hong Kong Special Administrative Region Government (No. 2020-76), and the Dean’s Research Fund (Ni. DRF/IRS-7/IRS-4) of The Education University of Hong Kong.

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