Valorization of e-waste via supercritical water technology: An approach for obsolete mobile phones

被引:2
|
作者
Botelho Meireles de Souza, Guilherme [1 ,2 ,3 ]
Bisinotto Pereira, Mariana [1 ]
Clementino Mourão, Lucas [2 ]
Gonçalves Alonso, Christian [2 ]
Jegatheesan, Veeriah [3 ]
Cardozo-Filho, Lucio [1 ,3 ,4 ]
机构
[1] Programa de Pós-Graduação Em Engenharia Química, Universidade Estadual de Maringá (UEM), Avenida Colombo, 5790 - Zona 7, PR, Maringá,87020-900, Brazil
[2] Programa de Pós-Graduação Em Engenharia Química, Universidade Federal de Goiás (UFG), Avenida Esperança, S/n - Chácaras de Recreio Samambaia, GO, Goiânia,74690-900, Brazil
[3] School of Engineering and Water: Effective Technologies and Tools (WETT) Research Centre, RMIT University, Melbourne,VIC,3000, Australia
[4] Escola de Engenharia, Universidade Estadual de São Paulo (UNESP), Avenida Professora Isette Corrêa Fontão, 505 - Jardim Das Flores, SP, São João da Boa Vista,13876-750, Brazil
基金
巴西圣保罗研究基金会;
关键词
Degradation rate - E-wastes - Electronics wastes - Metals recoveries - Organic degradation - Oxidizing agents - Supercritical water - Urban mining - Valorisation - Water technologies;
D O I
10.1016/j.chemosphere.2023.139343
中图分类号
学科分类号
摘要
The improper handling of electronic waste has not only severe environmental impacts but also results in the loss of high economic potential. To address this issue, the use of supercritical water (ScW) technology for the eco-friendly processing of waste printed circuit boards (WPCBs) obtained from obsolete mobile phones has been explored in this study. The WPCBs were characterized via MP-AES, WDXRF, TG/DTA, CHNS elemental analysis, SEM and XRD. A L9 Taguchi orthogonal array design was employed to evaluate the impact of four independent variables on the organic degradation rate (ODR) of the system. After optimization, an ODR of 98.4% was achieved at a temperature of 600 °C, a reaction time of 50 min, a flowrate of 7 mL min−1, and the absence of an oxidizing agent. The removal of the organic content from the WPCBs resulted in an increase in the metal concentration, with up to 92.6% of the metal content being efficiently recovered. During the ScW process, the decomposition by-products were continuously removed from the reactor system through the liquid or gaseous outputs. The liquid fraction, which was composed of phenol derivatives, was treated using the same experimental apparatus, achieving a total organic carbon reduction of 99.2% at 600 °C using H2O2 as the oxidizing agent. The gaseous fraction was found to contain hydrogen, methane, CO2, and CO as the major components. Finally, the addition of co-solvents, namely ethanol and glycerol, enhanced the production of combustible gases during the ScW processing of WPCBs. © 2023 Elsevier Ltd
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