Ultrafast conversion of carcinogenic 4-nitrophenol into 4-aminophenol in the dark catalyzed by surface interaction on BiPO4/g-C3N4 nanostructures in the presence of NaBH4

被引:20
作者
Azzam, Ahmed B. [1 ]
Djellabi, Ridha [2 ,3 ]
Sheta, Sheta M. [4 ]
El-Sheikh, S. M. [5 ]
机构
[1] Helwan Univ, Fac Sci, Chem Dept, Cairo 11795, Egypt
[2] Univ Milan, Dip Chim, Via Golgi 19, I-20133 Milan, Italy
[3] Univ Milan, INSTM UdR Milano, Via Golgi 19, I-20133 Milan, Italy
[4] Natl Res Ctr, Dept Inorgan Chem, 33 El Behouth St, Giza 12622, Egypt
[5] Cent Met R&D Inst CMRDI, Adv Mat Div, Nanomat & Nanotechnol Dept, POB 87, Cairo 11421, Egypt
关键词
GRAPHITIC CARBON NITRIDE; ENHANCED PHOTOCATALYTIC PERFORMANCE; VISIBLE-LIGHT; FACILE FABRICATION; MECHANISTIC INSIGHTS; IONIC LIQUID; REDUCTION; BIPO4; G-C3N4; NANOPARTICLES;
D O I
10.1039/d1ra02852a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The heterogeneous catalytic conversion of pollutants into useful industrial compounds is a two-goals at once process, which is highly recommended from the environmental, economic, and industrial points of view. In this regard, design materials with high conversion ability for a specific application is required to achieve such a goal. Herein, the synthesis conditions for the fabrication of BiPO4 nanorod bundles supported on g-C3N4 nanosheets as heterojunction composites was achieved using a facile ex situ chemical deposition for the reductive conversion of carcinogenic 4-nitrophenol (4-NP) into 4-aminophenol (4-AP). To better understand the mechanistic reduction pathways, BiPO4/g-C3N4 composites with varying ratios where obtained. The morphology and structure of BiPO4/g-C3N4 composites were checked using several methods: XRD, FE-SEM, HRTEM, XPS, and FT-IR, and it was found that hexagonal phase BiPO4 nanorod bundles were randomly distributed on the g-C3N4 nanosheets. Overall, the reduction ability of BiPO4/g-C3N4 composites was far better than bare BiPO4 and g-C3N4. A total reductive conversion of 4-NP at a concentration of 10 mg L-1 into 4-AP was found with 50% BiPO4/g-C3N4 composite within only one minute of reaction. Moreover, the presence of reducing agent (NaBH4) enhanced the kinetic rate constant up to 2.914 min(-1) using 50% BiPO4/g-C3N4, which was much faster than bare BiPO4 (0.052 min(-1)) or g-C3N4 (0.004 min(-1)). The effects of some operating parameters including the initial concentration of 4-NP and catalyst dosage were also evaluated during the experiments. BiPO4/g-C3N4 showed great stability and recyclability, wherein, the catalytic reduction efficiency remains the same after five runs. A plausible 4-NP reduction mechanism was discussed. The high catalytic activity with the good stability of BiPO4/g-C3N4 make it a potential candidate for the reduction of nitroaromatic compounds in real wastewaters.
引用
收藏
页码:18797 / 18808
页数:12
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