Mxene-decorated spinel oxides as innovative activators of peroxymonosulfate for degradation of caffeine in WWTP effluents: Insights into mechanisms

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F24%3A00137730" target="_blank" >RIV/00216224:14310/24:00137730 - isvavai.cz</a>

Výsledek na webu

<a href="https://www.sciencedirect.com/science/article/pii/S1385894724093057" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1385894724093057</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1016/j.cej.2024.157814" target="_blank" >10.1016/j.cej.2024.157814</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Mxene-decorated spinel oxides as innovative activators of peroxymonosulfate for degradation of caffeine in WWTP effluents: Insights into mechanisms

Popis výsledku v původním jazyce

In the frame of the environmental issues related to the efficiency of wastewaters treatment, the generation of advanced oxidation processes (AOPs) by 2D materials appears one of the most promising solutions. In this study, a novel catalytic system for peroxymonosulfate activation (PMS) was designed based on MXene (Ti3C2Tx) decorated with spinel oxides Co3O4, Fe3O4 and CoFe2O4 catalysts. Their efficiency in caffeine (CAF) degradation via PMS activation was assessed. The insertion of spinel oxides inside the multilayer structure of MXene along with their uniform surface decoration was demonstrated by SEM and TEM analyses and it also avoided the aggregation of the magnetic particles, thus increasing their efficiency. Among the different catalysts, the MXene/CoFe2O4 (MXCF) stood out as the most effective, mainly due to the Fe and Co redox cycles. The complete degradation of CAF was achieved in the dark within 10 min at natural pH using 0.2 g/L of MXCF and 0.5 mM of PMS. The novelty of current study lies in the efficient activation of PMS by, for the first time, MXCF in the dark along with mechanistic elucidation of PMS activation. The important role of Co3+/Co2+ and Fe3+/Fe2+ redox cycles alongside surface bound functional groups were highlighted. Radical scavenging and EPR experiments confirmed •OH and 1O2 as the main ROS involved in the CAF degradation. The CAF degradation pathways pointed to hydroxylation and imidazole ring opening mechanisms and MXCF catalyst also exhibited high efficiency in the degradation of sulfamethoxazole and phenol via PMS activation. To further highlight the relevance of the obtained results, treatment of tertiary effluents of wastewaters treatment plant (WWTP) in Bratislava contaminated by CAF exhibited a complete pollutant degradation after 3 h by supplying 0.2 g/L of catalyst and 2 mM PMS in the dark.

Název v anglickém jazyce

Mxene-decorated spinel oxides as innovative activators of peroxymonosulfate for degradation of caffeine in WWTP effluents: Insights into mechanisms

Popis výsledku anglicky

In the frame of the environmental issues related to the efficiency of wastewaters treatment, the generation of advanced oxidation processes (AOPs) by 2D materials appears one of the most promising solutions. In this study, a novel catalytic system for peroxymonosulfate activation (PMS) was designed based on MXene (Ti3C2Tx) decorated with spinel oxides Co3O4, Fe3O4 and CoFe2O4 catalysts. Their efficiency in caffeine (CAF) degradation via PMS activation was assessed. The insertion of spinel oxides inside the multilayer structure of MXene along with their uniform surface decoration was demonstrated by SEM and TEM analyses and it also avoided the aggregation of the magnetic particles, thus increasing their efficiency. Among the different catalysts, the MXene/CoFe2O4 (MXCF) stood out as the most effective, mainly due to the Fe and Co redox cycles. The complete degradation of CAF was achieved in the dark within 10 min at natural pH using 0.2 g/L of MXCF and 0.5 mM of PMS. The novelty of current study lies in the efficient activation of PMS by, for the first time, MXCF in the dark along with mechanistic elucidation of PMS activation. The important role of Co3+/Co2+ and Fe3+/Fe2+ redox cycles alongside surface bound functional groups were highlighted. Radical scavenging and EPR experiments confirmed •OH and 1O2 as the main ROS involved in the CAF degradation. The CAF degradation pathways pointed to hydroxylation and imidazole ring opening mechanisms and MXCF catalyst also exhibited high efficiency in the degradation of sulfamethoxazole and phenol via PMS activation. To further highlight the relevance of the obtained results, treatment of tertiary effluents of wastewaters treatment plant (WWTP) in Bratislava contaminated by CAF exhibited a complete pollutant degradation after 3 h by supplying 0.2 g/L of catalyst and 2 mM PMS in the dark.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

21001 - Nano-materials (production and properties)

Projekt

<a href="/cs/project/LM2023039" target="_blank" >LM2023039: Centrum výzkumu a vývoje plazmatu a nanotechnologických povrchových úprav</a><br>

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2024

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Chemical Engineering Journal

ISSN

1385-8947

e-ISSN

1873-3212

Svazek periodika

502

Číslo periodika v rámci svazku

December

Stát vydavatele periodika

CH - Švýcarská konfederace

Počet stran výsledku

13

Strana od-do

157814

Kód UT WoS článku

001365970300001

EID výsledku v databázi Scopus

2-s2.0-85209926546