Using a Surface-Response Approach to Optimize the Photocatalytic Activity of rGO/g-C3N4 for Bisphenol A Degradation

Author:

Xavier Chubraider1,Lopes Bianca Rebelo2,Lima Cleyryson de Sousa1,Ribeiro Caue3ORCID,Azevedo Eduardo Bessa1

Affiliation:

1. Laboratório de Desenvolvimento de Tecnologias Ambientais (LDTAmb), Chemistry Institute of São Carlos (IQSC), University of São Paulo (USP), Avenida Trabalhador São-Carlense, 400—Centro, P.O. Box 780, São Carlos 13560-970, SP, Brazil

2. Department of Chemistry (DQ), Separare–Núcleo de Pesquisa em Cromatografia, Federal University of São Carlos (UFSCar), Rodovia Washington Luis, s/nº km 235—Monjolinho, P.O. Box 676, São Carlos 13565-905, SP, Brazil

3. Laboratório de Nanotecnologia para o Agronegócio—LNNA, Embrapa Instrumentation—Brazilian Agricultural Research Corporation, Rua XV de Novembro, nº 1.452—Centro, P.O. Box 741, São Carlos 13560-970, SP, Brazil

Abstract

Although environmental and clean energy research has identified graphitic carbon nitride impregnated with reduced graphene oxide (rGO/g-C3N4) as a potential, efficient non-metallic photocatalyst, its efficacy against Contaminants of Emerging Concern (CECs) is relatively unknown. This study reports an optimized photocatalyst (response surface methodology, RSM) to remove the plasticizer and endocrine disruptor bisphenol A (BPA) from water. The synthetic procedure included sonication of prepared particles of g-C3N4 and graphite oxide (rGO), followed by reduction with hydrazine (24 h reflux), increasing specific surface areas, and improving synthesis reproducibility. In optimal conditions, the produced photocatalyst (50 mg L–1) removed 90% of BPA (100 mL, 100 μg L−1) in 90 min (30 min in the dark + 60 min irradiated) using a UV source (centered at 365 nm, 26 W) and exhibiting pseudo-first-order kinetics. For comparison purposes, under the same experimental conditions, pure g-C3N4 removed 50% of the BPA solution. Radical scavenging tests identified the superoxide radical as the main reactive oxygen species involved in the degradation. Two major degradation products were identified by mass spectrometry, both of them less ecotoxic than BPA to a variety of test organisms, according to in silico estimations (ECOSAR 2.0).

Funder

The National Council for Scientific and Technological Development

The Coordination for the Improvement of Higher Education Personnel

São Paulo Research Foundation

The Research Network of Nanotechnology Applied to Agribusiness

Publisher

MDPI AG

Subject

Physical and Theoretical Chemistry,Catalysis,General Environmental Science

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