TY - JOUR
T1 - Simultaneous catalytic elimination of formaldehyde and ozone over one-dimensional rod-like manganese dioxide at ambient temperature
AU - Zhang, Yi
AU - Shi, Jin
AU - Fang, Wenjian
AU - Chen, Mingxia
AU - Zhang, Zhixiang
AU - Jiang, Zhi
AU - Shangguan, Wenfeng
AU - Einaga, Hisahiro
N1 - Funding Information:
This work was supported by the National Key Research & Development Plan (2017YFC0211804) and the National Natural Science Foundation of China (21577088).
Publisher Copyright:
© 2019 Society of Chemical Industry
PY - 2019/7
Y1 - 2019/7
N2 - Background: Formaldehyde (HCHO) and ozone (O3) are seriously hazardous materials to human health, especially in the indoor environment, and need to be inhibited. Manganese dioxide (MnO2) catalysts have been extensively studied in the field of environmental pollution owing to their various morphologies and crystal structures. In this study, one-dimensional rod-like MnO2 catalysts were prepared by a hydrothermal method. The crystal form and other factors affecting the activity were explored through an activity test and various characterization methods. The decomposition process of HCHO and O3 on the most active catalyst was analyzed by in situ diffuse reflection infrared Fourier transform spectroscopy (DRIFTS). Results: α-MnO2 displayed the best catalytic performance and achieved 90% HCHO conversion, 100% carbon dioxide (CO2) yield and 100% O3 decomposition under different experimental conditions. The characterization results illustrated that the crystal phase of α-MnO2 has a suitable tunnel structure for HCHO adsorption, also leading to greater mobility of adsorbed oxygen species, abundant oxygen vacancies and active surface oxygen species, which could be the reason for the superior catalytic performance of α-MnO2. Formate and dioxymethylene (DOM) species were identified as the dominant intermediates by in situ DRIFTS. The surface hydroxyl (OH) group was confirmed to play an essential role in the complete oxidation of carbonaceous intermediates into harmless CO2 and water (H2O). Conclusion: α-MnO2 exhibited the best catalytic performance among the as-prepared samples and can efficiently eliminate HCHO and O3 in the environment.
AB - Background: Formaldehyde (HCHO) and ozone (O3) are seriously hazardous materials to human health, especially in the indoor environment, and need to be inhibited. Manganese dioxide (MnO2) catalysts have been extensively studied in the field of environmental pollution owing to their various morphologies and crystal structures. In this study, one-dimensional rod-like MnO2 catalysts were prepared by a hydrothermal method. The crystal form and other factors affecting the activity were explored through an activity test and various characterization methods. The decomposition process of HCHO and O3 on the most active catalyst was analyzed by in situ diffuse reflection infrared Fourier transform spectroscopy (DRIFTS). Results: α-MnO2 displayed the best catalytic performance and achieved 90% HCHO conversion, 100% carbon dioxide (CO2) yield and 100% O3 decomposition under different experimental conditions. The characterization results illustrated that the crystal phase of α-MnO2 has a suitable tunnel structure for HCHO adsorption, also leading to greater mobility of adsorbed oxygen species, abundant oxygen vacancies and active surface oxygen species, which could be the reason for the superior catalytic performance of α-MnO2. Formate and dioxymethylene (DOM) species were identified as the dominant intermediates by in situ DRIFTS. The surface hydroxyl (OH) group was confirmed to play an essential role in the complete oxidation of carbonaceous intermediates into harmless CO2 and water (H2O). Conclusion: α-MnO2 exhibited the best catalytic performance among the as-prepared samples and can efficiently eliminate HCHO and O3 in the environment.
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U2 - 10.1002/jctb.6023
DO - 10.1002/jctb.6023
M3 - Article
AN - SCOPUS:85065438314
SN - 0268-2575
VL - 94
SP - 2305
EP - 2317
JO - Journal of Chemical Technology and Biotechnology
JF - Journal of Chemical Technology and Biotechnology
IS - 7
ER -