In this work, iron-containing sludge is used to prepare iron-based catalysts for efficient HS selective catalytic oxidation. First, the effect of calcination temperatures on the catalytic activities of HS selective oxidation is carried out and it can be found that S-500 calcined at 500 °C performs excellent catalytic activity. Then, the catalytic performance of the S-500 catalyst is further optimized using alkaline treatment with different concentrations of NaOH solution. The results indicate that S-500(2.0) treated with 2 M NaOH solution has the highest catalytic activity of HS selective oxidation. Next, various characterization methods are used to analyze the structure and physical-chemical of the sludge-based catalysts. N-Brunauer-Emmett-Teller (N-BET) and X-ray photoelectron spectroscopy analyses show that the S-500(2.0) catalyst has the smallest average particle (11.17 nm), the biggest ratio of / (17.98) with bigger external specific surface area (49.09 m·g), a higher proportion of Fe species (50.88%), and surface adsorbed oxygen species (48.07%). Meanwhile, O-TPD and CO-TPD analysis indicates that the S-500(2.0) catalyst has a bigger value of the O/O ratio (50.56%) and (CO) /(CO) ratio of (31.41%), indicating that there are much more oxygen vacancies and weak alkaline sites. As a result, the excellent catalytic performance of HS selective oxidation can be attributed to its outstanding physical-chemical properties.
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http://dx.doi.org/10.1021/acsomega.4c03115 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Shanghai Advanced Research Institute Chinese Academy of Sciences: Chinese Academy of Sciences Shanghai Advanced Research Institute, Low-Carbon Conversion Science and Engineering Cente, 100 Haike Road, 201203, Shanghai, CHINA.
Renewable energy-driven electrochemical CO2 reduction has emerged as a promising technology for a sustainable future. However, achieving efficient production of storable liquid fuels at ampere-level current densities remains a significant hurdle in the large-scale implementation of CO2 electroreduction. Here we report a novel catalytic electrode comprising chlorine-doped SnO2 nanoflowers arrayed on the exterior of three-dimensional nickel hollow fibers.
View Article and Find Full Text PDFJ Mol Model
January 2025
School of Chemistry & Chemical Engineering, Linyi University, Linyi, 276000, China.
Context: In this work, a comparative study on the catalytic conversion of 5-hydroxymethyl furfural (HMF) to 2,5-bis(hydroxymethyl)furan (BHMF) on precious Pd(111) and nonprecious Cu(111) was systematically performed. On the basis of the calculated activation energy (E) and reaction energy (E), the optimal energy path for the hydrogenation of HMF (F-CHO) into BHMF (F-CHOH) on Pd(111) is as follows: F-CHO + 2H → F-CHOH + H → F-CHOH; the minimum reaction path on Cu(111) is F-CHO + 2H → F-CHO + H → F-CHOH. On Cu(111), the formation of F-CHOH from F-CHO hydrogenation is the rate-determining step because it has the highest reaction energy barrier and the smallest rate constant.
View Article and Find Full Text PDFEnviron Sci Technol
January 2025
Research Center for Carbon-Neutral Environmental & Energy Technology, Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu 611731, China.
As primary air pollutants from fossil fuel combustion, the excess emission of nitric oxides (NO) results in a series of atmospheric environmental issues. Although the selective catalytic reduction technology has been confirmed to be effective for NO removal, green purification and value-added conversion of NO under ambient conditions are still facing great challenges, especially for nitrogen resource recovery. To address that, photo-/electrocatalysis technology offers sustainable routes for efficient NO purification and upcycling under ambient temperature and pressure, which has received considerable attention from scientific communities.
View Article and Find Full Text PDFOrg Biomol Chem
January 2025
Department of Chemistry, Indian Institute of Technology Kharagpur, Kharagpur 721 302, India.
The "catalytic triad" present at the active site of ribonuclease A (RNase A) is responsible for the cleavage of the 5'-phosphodiester bond; amino acid residues His12, Lys41 and His119 constituting this triad provide a positively charged environment at the physiological pH. Based on docking studies, 1,4,5-trisubstituted-carboxylated 1,2,3-triazoles (1,4,5-TTs) were identified as a new class of RNase A inhibitors. Therefore, two different groups of 1,4,5-TTs, functionalized with carboxylic acid groups, were synthesized by reacting pre functionalized butyne-1,4-diol derivatives with several aryl/alkyl azides under solvent and catalyst free conditions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
University of Oxford, Chemistry, 12 Mansfield Road, OX1 3TA, Oxford, UNITED KINGDOM OF GREAT BRITAIN AND NORTHERN IRELAND.
In homogeneous catalysis, uncovering structure-activity relationships remains very rare but invaluable to understand and rationally improve performances. Here, generalizable structure-activity relationships apply to a series of heterodinuclear polymerization catalysts featuring Co(III) and s-block metals M(I/II) (M= Na(I), K(I), Ca(II), Sr(II), Ba(II)). These are shown to apply to polycarbonate production by the ring-opening copolymerizations (ROCOP) of cyclohexene oxide (CHO) and carbon dioxide (CO2), conducted at high (20 bar) and low (1 bar) CO2 pressures, and to polyester production by copolymerization of cyclohexene oxide and phthalic anhydride (PA).
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