首页|基于正交实验探究Fe-Beta分子筛催化剂SCR脱硝性能

基于正交实验探究Fe-Beta分子筛催化剂SCR脱硝性能

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该研究采用正交实验探究并制备性能优异的Fe-Beta催化剂用于高效脱除氮氧化物.通过合成一系列Fe-Beta 催化剂,并考察其在NH3选择性催化还原NOx反应中的催化性能,筛选出最优配方:硅铝比为30、固液比为1∶20 g·mL-1、采用 Fe(NO3)3·9H2O 制备的前驱体溶液浓度为 0.02 mol·L-1.Fe/Beta-30-1∶20(0.02)催化剂在 350~450 ℃内NO转化率在90%以上且具有优异的N2选择性.此外,Fe/Beta-30-1∶20(0.02)催化剂具有良好的抗SO2性和抗H2O性能以及优异的水热稳定性.表征结果表明,由于分子筛与金属离子之间存在协同作用,在Beta分子筛中添加适量的铁(2.18%)时,会增加SCR反应活性位点数量,拓宽活性温度窗口.同时,Fe-Beta催化剂具有较大的BET比表面积、较均匀的粒径尺寸以及孔径分布均匀,有助于NH3-SCR反应进行.
Investigation of SCR denitrification performance of Fe-Beta zeolite catalysts based on the orthogonal experiments
In this study,orthogonal experiments were used to investigate and prepare Fe-Beta catalysts with highly effective NOx removal.A series of Fe-Beta catalysts were synthesized,and their catalytic performance in the selective catalytic reduction of NOx reaction by NH3(NH3-SCR)was investigated,the optimal formulations were screened out as follows:the SiO2∶Al2O3 ratio of 30,the solid-liquid ratio of 1∶20 g·mL-1,and the precursor solution concentration of 0.02 mol·L-1 prepared with Fe(NO3)3.9H2O.The Fe/Beta-30-1∶20(0.02)catalyst showed higher than 90%NO conversion and had an excellent N2 selectivity within 350~450 ℃.In addition,the Fe/Beta-30-1∶20(0.02)catalyst had good SO2 resistance and H2O resistance as well as an excellent hydrothermal stability.The characterization results showed that the addition of Fe(2.18%)in the Beta zeolite enhanced the active sites for SCR reaction and widened the active temperature window due to the synergistic effects of zeolite and Fe ions.Meanwhile,the Fe-Beta catalyst possessed large BET specific surface area,more uniform particle size and pore size,which was conducive to the NH3-SCR reaction.

Fe-Betazeoliteselective catalytic reduction(SCR)orthogonal experimentanti-poisoning propertieshydrothermal stability

肖萌、岳俊杰、李彭辉、郭铭玉、赵英杰、刘博群、崔少平、高婧、牛可

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天津理工大学环境科学与安全工程学院,天津 300384

交通运输部天津水运工程科学研究院水路交通环境保护技术实验室,天津 300456

Fe-Beta催化剂 分子筛 选择性催化还原 正交实验 抗中毒性能 水热稳定性

2024

环境工程学报
中国科学院生态环境研究中心

环境工程学报

CSTPCD北大核心
影响因子:0.804
ISSN:1673-9108
年,卷(期):2024.18(10)