RESUMO
Dichloromethane (DCM), a typical representative of chlorinated volatile organic compounds (CVOCs), is usually exhausted along with other volatile organic compounds (VOCs), such as toluene and ethyl acetate, in industrial factories. To address the complexity of the components, the large variation in concentration of each component and the water content of the exhaust gases emitted from the pharmaceutical and chemical industries, the adsorption characteristics of DCM, toluene (MB), and ethyl acetate (EAC) vapors on hypercrosslinked polymeric resins (NDA-88) were studied by dynamic adsorption experiments. Furthermore, the adsorption characteristics of NDA-88 for binary vapor systems of DCM-MB and DCM-EAC at different concentration ratios and the nature of the interaction force with the three VOCs were explored. NDA-88 was found to be suitable for treating binary vapor systems of DCM mixed with low concentrations of MB/EAC, and a small quantity of adsorbed MB or EAC would promote the adsorption of DCM by NDA-88, which is attributed to the microporous filling phenomenon. Finally, the influence of humidity on the adsorption performance of binary vapor systems for NDA-88 and the regeneration adsorption performance of NDA-88 were investigated. The presence of water steam shortened the penetration times of DCM, EAC, and MB, regardless of whether it was in the DCM-EAC or DCM-MB two-component systems. This study has identified a commercially available hypercrosslinked polymeric resin NDA-88, which has excellent adsorption performance and regeneration capacity for both single-component DCM gas and a binary mixture of DCM-low-concentration MB/EAC, providing experimental guidance for the treatment of emissions from pharmaceutical and chemical industries by adsorption.
RESUMO
Herein, a series of niobium oxide supported cerium nanotubes (CeNTs) catalysts with different loading amount of Nb2O5 (0-10 wt.%) were prepared and used for selective catalytic reduction of NOx with NH3 (NH3-SCR) in the presence of CH2Cl2. Commercial V2O5-WO3-TiO2 catalyst was also prepared for comparison. The physcial properties and chemical properties of the Nb2O5 loaded cerium nanotubes catalysts were investigated by X-ray diffractometer, Transmission electron microscope, Brunauer-Emmett-Teller specific surface area, H2-temperature programmed reduction, NH3-temperature programmed desorption and X-ray photoelectron spectroscopy. The experiment results showed that the loading amount of Nb2O5 had a significant effect on the catalytic performance of the catalysts. 10 wt.% Nb-CeNTs catalyst presented the best NH3-SCR performance and degradation efficiency of CH2Cl2 among the prepared catalysts, due to its superior redox capability, abundant surface oxygen species and acid sites, the interaction between Nb and Ce, higher ratio of Nb4+/(Nb5++ Nb4+) and Ce3+/(Ce3+ + Ce4+), as well as the special tubular structure of cerium nanotube. This study may provide a practical approach for the design and synthesis of SCR catalysts for the simultaneously removal NOx and chlorinated volatile organic compounds (CVOCs) emitted from the stationary industrial sources.
Assuntos
Cério , Nanotubos , Amônia , Catálise , Cloreto de Metileno , Nióbio , Oxirredução , TitânioRESUMO
A core-shell catalyst which consists of a Co3O4 core and ZSM-5 shell, was prepared by microwave hydrothermal method and subjected for dichloromethane (DCM) oxidation. Chromium, cerium, niobium, and manganese species were separately introduced into the core-shell catalyst using the wet precipitation method and denoted as M-Co@Z (M = Cr, Ce, Nb, Mn). The catalytic activity of the Cr-Co@Z catalyst was significantly increased due to the interaction between Cr2O3 and Co3O4. The results of Raman spectra indicated the incorporation of chromium into the Co3O4 lattice and revealed the existence of the interaction between Cr2O3 and Co3O4. The synergistic effect between Cr2O3 and Co3O4 might be conducive to the generation of highly defective structure and increase the ratio of Co3+/Co2+ of the sample, leading to its better oxygen mobility. The dechlorination ability of Cr-Co@Z was also promoted due to the enhanced mobility of lattice oxygen. Based on in situ DRIFT studies, a possible reaction route of CH2Cl2 oxidation over Cr-Co@Z catalyst was proposed.
