首页|Efficient nitric oxide capture and reduction on Ni-loaded CHA zeolites

Efficient nitric oxide capture and reduction on Ni-loaded CHA zeolites

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As a prominent contributor to air pollution,nitric oxide(NO)has emerged as a critical agent causing detrimental environmental and health ramifications.To mitigate emissions and facilitate downstream utilization,adsorption-based techniques offer a compelling approach for direct NO capture from both stationary and mobile sources.In this study,a comprehensive exploration of NO capture under oxygen-lean and oxygen-rich conditions was conducted,employing Ni ion-exchanged chabazite(CHA-type)zeolites as the adsorbents.Remarkably,Ni/Na-CHA zeolites,with Ni loadings ranging from 3 to 4 wt%,demonstrate remarkable dynamic uptake capacities and exhibit exceptional NO capture efficiencies(NO-to-Ni ratio)for both oxygen-lean(0.17-0.31 mmol/g,0.32-0.43 of NO/Ni)and oxygen-rich(1.64-1.18 mmol/g)under ambient conditions.An NH3 reduction methodology was designed for the regeneration of absorbents at a relatively low temperature of 673 K.Comprehensive insights into the NOx adsorption mechanism were obtained through temperature-programmed desorption experiments,in situ Fourier transform infrared spectroscopy,and density functional theory calculations.It is unveiled that NO and NO2 exhibit propensity to coordinate with Ni2+via N-terminal or O-terminal,yielding thermally stable complexes and metastable species,respectively,while the low-temperature desorption substances are generated in close proximity to Na+.This study not only offers micro-level perspectives but imparts crucial insights for the advancement of capture and reduction technologies utilizing precious-metal-free materials.

Nitrogen oxidesCaptureZeoliteLean/rich conditionAdsorption mechanism

Bin Yue、Jianhua Wang、Shanshan Liu、Guangjun Wu、Bin Qin、Landong Li

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School of Materials Science and Engineering,Nankai University,Tianjin,300350,China

College of Chemistry,Nankai University,Tianjin,300071,China

2024

绿色能源与环境(英文)

绿色能源与环境(英文)

CSTPCD
ISSN:
年,卷(期):2024.9(12)