Resource utilization of medical waste incineration fly ash to activate peroxydisulfate for tetracycline degradation: Synergy between adsorption and PDS activation

Medical waste incineration fly ash (MWI FA) is classified as a hazardous solid waste. Therefore, the development of recycling technologies to convert MWI FA into useful products is necessary and challenging. In this study, we developed a sustainable approach for preparing a catalyst through the pyro...

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Veröffentlicht in:Environmental research 2024-10, Vol.258, p.119488, Article 119488
Hauptverfasser: Fang, Xiaolin, Zhang, Guichang, Zhang, Xiaoping, He, Songwen, Xu, Wei, Zhang, Xin, Zhong, Siqi
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container_start_page 119488
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creator Fang, Xiaolin
Zhang, Guichang
Zhang, Xiaoping
He, Songwen
Xu, Wei
Zhang, Xin
Zhong, Siqi
description Medical waste incineration fly ash (MWI FA) is classified as a hazardous solid waste. Therefore, the development of recycling technologies to convert MWI FA into useful products is necessary and challenging. In this study, we developed a sustainable approach for preparing a catalyst through the pyrolysis of water-washed MWI FA (WW FA-x, where x corresponds to the pyrolysis temperature). Subsequently, it was applied as a potent peroxydisulfate (PDS) activator to remove tetracycline (TC) from water. The results showed that the WW FA-800 exhibited remarkable adsorption performance as well as highly efficient catalytic activation of PDS, with a 115 mg/g maximum TC adsorption capacity and 93.5% (reaction kinetic rate = 315 μmol/g/h) TC removal within 60 min. A synergistic effect was achieved by adsorption and PDS activation. TC degradation was primarily driven by non-radical (1O2 and electron transfer) processes. WW FA-800 possesses multiple active sites, including defects, π–π*, O–CO groups, Fe0, and Cu(I). Three possible pathways for TC decomposition have been proposed, with the majority of intermediates exhibiting less toxicity than TC. Furthermore, the WW FA/PDS system exhibited an excellent anti-interference ability, and universality in the degradation of various organic contaminants. Notably, energy consumption was minimal, approximately 2.80 kWh/(g·TC), and the leachability of heavy metals in the WW FA-800 was within acceptable limits. This study provides a MWI FA recycling route for the development of highly active catalysts. [Display omitted] •WW FA-800 catalyst was fabricated from medical waste incineration fly ash.•WW FA-800 was used to remove TC via the synergistic action of adsorption and degradation.•Singlet oxygen (1O2) and electron transfer dominated the WW FA-800/PDS oxidization system.•A green and cost-effective method was proposed to recycle MWI FA and remove organic pollutants.
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Therefore, the development of recycling technologies to convert MWI FA into useful products is necessary and challenging. In this study, we developed a sustainable approach for preparing a catalyst through the pyrolysis of water-washed MWI FA (WW FA-x, where x corresponds to the pyrolysis temperature). Subsequently, it was applied as a potent peroxydisulfate (PDS) activator to remove tetracycline (TC) from water. The results showed that the WW FA-800 exhibited remarkable adsorption performance as well as highly efficient catalytic activation of PDS, with a 115 mg/g maximum TC adsorption capacity and 93.5% (reaction kinetic rate = 315 μmol/g/h) TC removal within 60 min. A synergistic effect was achieved by adsorption and PDS activation. TC degradation was primarily driven by non-radical (1O2 and electron transfer) processes. WW FA-800 possesses multiple active sites, including defects, π–π*, O–CO groups, Fe0, and Cu(I). Three possible pathways for TC decomposition have been proposed, with the majority of intermediates exhibiting less toxicity than TC. Furthermore, the WW FA/PDS system exhibited an excellent anti-interference ability, and universality in the degradation of various organic contaminants. Notably, energy consumption was minimal, approximately 2.80 kWh/(g·TC), and the leachability of heavy metals in the WW FA-800 was within acceptable limits. This study provides a MWI FA recycling route for the development of highly active catalysts. [Display omitted] •WW FA-800 catalyst was fabricated from medical waste incineration fly ash.•WW FA-800 was used to remove TC via the synergistic action of adsorption and degradation.•Singlet oxygen (1O2) and electron transfer dominated the WW FA-800/PDS oxidization system.•A green and cost-effective method was proposed to recycle MWI FA and remove organic pollutants.</description><identifier>ISSN: 0013-9351</identifier><identifier>ISSN: 1096-0953</identifier><identifier>EISSN: 1096-0953</identifier><identifier>DOI: 10.1016/j.envres.2024.119488</identifier><identifier>PMID: 38925468</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Adsorption ; catalysts ; electron transfer ; energy ; fly ash ; Medical waste incineration fly ash ; Peroxydisulfate activation ; pyrolysis ; solid wastes ; synergism ; temperature ; tetracycline ; Tetracycline degradation ; toxicity ; waste incineration</subject><ispartof>Environmental research, 2024-10, Vol.258, p.119488, Article 119488</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024. 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Therefore, the development of recycling technologies to convert MWI FA into useful products is necessary and challenging. In this study, we developed a sustainable approach for preparing a catalyst through the pyrolysis of water-washed MWI FA (WW FA-x, where x corresponds to the pyrolysis temperature). Subsequently, it was applied as a potent peroxydisulfate (PDS) activator to remove tetracycline (TC) from water. The results showed that the WW FA-800 exhibited remarkable adsorption performance as well as highly efficient catalytic activation of PDS, with a 115 mg/g maximum TC adsorption capacity and 93.5% (reaction kinetic rate = 315 μmol/g/h) TC removal within 60 min. A synergistic effect was achieved by adsorption and PDS activation. TC degradation was primarily driven by non-radical (1O2 and electron transfer) processes. WW FA-800 possesses multiple active sites, including defects, π–π*, O–CO groups, Fe0, and Cu(I). Three possible pathways for TC decomposition have been proposed, with the majority of intermediates exhibiting less toxicity than TC. Furthermore, the WW FA/PDS system exhibited an excellent anti-interference ability, and universality in the degradation of various organic contaminants. Notably, energy consumption was minimal, approximately 2.80 kWh/(g·TC), and the leachability of heavy metals in the WW FA-800 was within acceptable limits. This study provides a MWI FA recycling route for the development of highly active catalysts. 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[Display omitted] •WW FA-800 catalyst was fabricated from medical waste incineration fly ash.•WW FA-800 was used to remove TC via the synergistic action of adsorption and degradation.•Singlet oxygen (1O2) and electron transfer dominated the WW FA-800/PDS oxidization system.•A green and cost-effective method was proposed to recycle MWI FA and remove organic pollutants.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>38925468</pmid><doi>10.1016/j.envres.2024.119488</doi></addata></record>
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subjects Adsorption
catalysts
electron transfer
energy
fly ash
Medical waste incineration fly ash
Peroxydisulfate activation
pyrolysis
solid wastes
synergism
temperature
tetracycline
Tetracycline degradation
toxicity
waste incineration
title Resource utilization of medical waste incineration fly ash to activate peroxydisulfate for tetracycline degradation: Synergy between adsorption and PDS activation
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