Nitrate reduction with bimetallic catalysts. A stability-addressed overview

被引:36
作者
Sanchis, I [1 ]
Diaz, E. [1 ]
Pizarro, A. H. [1 ]
Rodriguez, J. J. [1 ]
Mohedano, A. F. [1 ]
机构
[1] Univ Autonoma Madrid, Dept Chem Engn, Campus Cantoblanco, Madrid 28049, Spain
关键词
Nitrate; Catalytic reduction; Catalyst deactivation; Regeneration; CATALYTIC-REDUCTION; PD-CU; AQUEOUS NITRATE; DRINKING-WATER; ACTIVATED CARBON; NITRITE REDUCTION; SELECTIVE HYDROGENATION; NATURAL-WATER; PT-CU; PALLADIUM CATALYSTS;
D O I
10.1016/j.seppur.2022.120750
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Nitrate (NO3-) pollution of water bodies is a serious environmental problem worldwide. One of the major concerns about NO3- contamination is the lack of cost-effective solutions for its removal from potential drinking water resources. Current technologies, such as ion exchange, reverse osmosis and electrodialysis, produce a reject with high NO3- concentration. Catalytic reduction is an emerging technology, capable of transforming NO3- into harmless N-2. A critical issue is to achieve almost complete selectivity to this last species so that the final concentrations of NO2- and NH4+ can fit the stringent allowed limits. Numerous studies have been carried out evaluating the activity and N-2 selectivity of bimetallic catalysts. Catalyst deactivation by surface fouling, irreversible oxidation of the metal promoter, metal leaching and aggregation of metallic particles remain a major challenge for full-scale implementation of catalytic nitrate reduction. Therefore, it is necessary to develop highly stable catalyst and/or effective solutions for catalyst regeneration. The existing literature on this respect is reviewed hereby.
引用
收藏
页数:10
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