Copper species were incorporated into SBA-15 by solid-state grinding precursor with as-prepared mesoporous silica (SPA). The obtained materials (CuAS) were well-characterized by XRD, TEM, N(2) adsorption, H(2)-TPR, IR, and TG and compared with the material derived from calcined SBA-15 (CuCS). Surprisingly, CuO up to 6.7 mmol·g(-1) can be highly dispersed on SBA-15 by use of SPA strategy. Such CuO forms a smooth layer coated on the internal walls of SBA-15, which contributes to the spatial order and results in less-blocked mesopores. However, the aggregation of CuO takes place in CuCS material containing 6.7 mmol·g(-1) copper, which generates large CuO particles of 21.4 nm outside the mesopores. We reveal that the high dispersion extent of CuO is ascribed to the abundant silanols, as well as the confined space between template and silica walls provided by as-prepared SBA-15. The SPA strategy allows template removal and precursor conversion in one step, avoids the repeated calcination in conventional modification process, and saves time and energy. We also demonstrate that the CuAS material after autoreduction exhibits much better adsorptive desulfurization capacity than CuCS. Moreover, the adsorption capacity of regenerated adsorbent can be recovered completely.
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http://dx.doi.org/10.1021/la101856d | DOI Listing |
ACS Appl Mater Interfaces
December 2024
Oil & Gas Field Applied Chemistry Key Laboratory of Sichuan Province, College of Chemistry and Chemical Engineering, Southwest Petroleum University, Chengdu 610500, China.
In this study, waste polystyrene was modified and upgraded to prepare formylated polystyrene, and the modified polystyrene acetyl hydrazone (LT-HPA) was synthesized by condensation with polymethyl-propionyl-hydrazine. It is proven that the modification of the adsorption material is successful by various characterization methods. In the subsequent pollutant removal study, pH, mass, concentration, contact time, and salt ion interference were investigated.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
School of Materials Science and Engineering, National Institute for Advanced Materials, TKL of Metal and Molecule-Based Material Chemistry, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin, 300350, China.
Metal-organic frameworks (MOFs) have great prospects as adsorbents for industrial gas purification, but often suffer from issues of water stability and competitive water adsorption. Herein, we present a hydrolytically stable MOF that could selectively capture and recover trace SO from flue gas, and exhibits remarkable recyclability in the breakthrough experiments under wet flue-gas conditions, due to its excellent resistance to the corrosion of SO and the water-derived capillary forces. More strikingly, its SO capture efficiency is barely influenced by the increasing humidity, even if the pore filling with water is reached.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou, Fujian, 350108, P. R. China.
Understanding the relationship of competitive adsorption between reactants is the prerequisite for high activity and selectivity in heterogeneous catalysis, especially the difference between the adsorption energies (E) of two reactive intermediates in Langmuir-Hinshelwood (L-H) models. Using oxidative dehydrogenation of hydrogen sulfide (HS-ODH) as a probe, we develop various metal single atoms on nitrogen-doped carbon (M-NDC) catalysts for controlling E-HS, E-O and investigating the difference in activity and selectivity. Combining theoretical and experimental results, a Sabatier relationship between the catalytic performance and E-O/E-HS emerges.
View Article and Find Full Text PDFEnviron Technol
November 2024
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, People's Republic of China.
Crystal α-FeOOH and amorphous α-FeOOH were obtained at different preparation temperatures, and low temperature desulfurization tests were carried out respectively. The results were characterized by XRD, BET, FT-IR and UV-vis. When the preparation temperature is 10-20℃, α-FeOOH is a crystalline structure composed of large grains, and when the preparation temperature is -5-5℃, α-FeOOH is an amorphous structure composed of small grains.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Instituto de Química, Universidad Nacional Autónoma de México Ciudad Universitaria, Ciudad de México, 04510 México.
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