Carbamazepine degradation by visible-light-driven photocatalyst Ag3PO4/GO: Mechanism and pathway.

Carbamazepine (CBZ), as one of the most frequently detected pharmaceuticals, is of great concern due to its potential impact on the ecosystem and human health. This study provides an effective approach to remove CBZ by using photocatalyst silver phosphate combined with graphene oxide (Ag3PO4/GO) under visible irradiation. The morphology, composition, and optical properties of Ag3PO4/GO were characterized employing SEM, XRD, and DRS. Graphene oxide could improve the visible-light utilization and promote electron's charge to enhance the photocatalytic performance of Ag3PO4/GO. With the optimal reaction condition of 5.86 mW/cm2 light intensity, 15-25 °C temperature, 5-7 pH, and 0.5 mg/L catalytic dosages, 5 mg/L CBZ could be completely degraded in 30 min, and the apparent rate constant could reach 0.12 min-1. Additionally, the radical trapping experiments indicated •OH and O2-• were the main reactive oxygen species employed to eliminate CBZ. The decay pathways of CBZ had been proposed accordingly, and the main product was the low-molecular products.

Photocatalytic degradation of ketoconazole by Z-scheme Ag3PO4/graphene oxide: response surface modeling and optimization.

Ketoconazole is an imidazole fungicide which is commonly used as pharmaceutical and healthcare products. Residual amount of this compound can cause adverse ecological health problems. The present study investigated ketoconazole photocatalytic degradation using Ag3PO4/graphene oxide (GO). Ag3PO4/GO and Ag3PO4 as visible light-driven photocatalysts was synthesized using the in situ growth method. Degradation of ketoconazole at the concentration of 1-20 mg/L in aqueous solutions was optimized in the presence of Ag3PO4/GO nanocomposite with the dosage of 0.5-2 g/L, contact time of 15-20 min, and pH of 5-9 using response surface methodology. A second-order model was selected as the best fitted model with R2 value and lack of fit as 0.935 and 0.06, respectively. Under the optimized conditions, the Ag3PO4/GO catalyst achieved a photocatalytic efficiency of 96.53% after 93.34 min. The photocatalytic activity, reaction kinetics, and stability were also investigated. The results indicated that the Ag3PO4/GO nanocomposite exhibited higher photocatalytic activity for ketoconazole degradation, which was 2.4 times that of pure Ag3PO4. Finally, a direct Z-scheme mechanism was found to be responsible for enhanced photocatalytic activity in the Ag3PO4/GO nanocomposite. The high photocatalytic activity, acceptable reusability, and good aqueous stability make the Ag3PO4/GO nanocomposite a promising nanophotocatalyst for photocatalytic degradation of azoles contaminants.

Synthesis of silver phosphate/graphene oxide composite and its enhanced visible light photocatalytic mechanism and degradation pathways of tetrabromobisphenol A.

In the present study, silver phosphate/graphene oxide (Ag3PO4/GO) composite was synthesized by ultrasound-precipitation processes. Afterwards, physicochemical properties of the resulting samples were studied through scanning electron microscope, transmission electron microscope, X-ray diffraction, N2 adsorption/desorption, UV-vis diffuse reflectance spectroscopy, Raman spectroscopy, X-ray photoelectron spectroscopy, surface photovoltage spectroscopy and photoelectrochemical measurements. Results indicated that spherical Ag3PO4 displayed an average diameter of 150 nm and body-centered cubic crystal phase, which was integrated with GO. In addition, the visible light absorbance, charge separation efficiency and lifetime of Ag3PO4 were significantly improved by integration with GO. In addition, Ag3PO4/GO composite was applied to decompose tetrabromosphenol A (TBBPA) in water body. It was found that TBBPA could be completely decomposed within 60 min illumination. Furthermore, several scavenger experiments were conducted to distinguish the contribution of reactive species to the photoctalytic efficiency. Moreover, the enhanced visible light mechanism of Ag3PO4/GO was proposed and discussed. Eventually, several PC decomposition pathways of TBBPA were identified including directly debromination and oxidation, and subsequently further oxidation and hydroxylation processes.

Synthesis and characterization of Ag3PO4 immobilized with graphene oxide (GO) for enhanced photocatalytic activity and stability over 2,4-dichlorophenol under visible light irradiation.

A series of visible-light responsive photocatalysts prepared using Ag3PO4 immobilized with graphene oxide (GO) with varying GO content were obtained by an electrostatically driven method, and 2,4-dichlorophenol (2,4-DCP) was used to evaluate the performance of the photocatalysts. The composites exhibited superior photocatalytic activity and stability compared with pure Ag3PO4. When the content of GO was 5%, the degradation efficiency of 2,4-DCP could reach 98.95%, and 55.91% of the total organic (TOC) content was removed within 60 min irradiation. Meanwhile, the efficiency of 91.77% was achieved for 2,4-DCP degradation even after four times of recycling in the photocatalysis/Ag3PO4-GO (5%) system. Reactive species of O2(˙-), OH˙ and h(+) were considered as the main participants for oxidizing 2,4-DCP, as confirmed by the free radical capture experiments. And some organic intermediates including 4-chlorophenol (4-CP), hydroquinone (HQ), benzoquinone (BZQ), 2-chlorohydroquinone and hydroxyhydroquinone (HHQ) were detected by comparison with the standard retention times from the high performance liquid chromatography (HPLC). In short, the enhanced photocatalytic property of Ag3PO4-GO was closely related to the strong absorption ability of GO relative to 2,4-DCP, the effective separation of photogenerated electron-hole pairs, and the excellent electron capture capability of GO.