Indirect electrocatalytic conversion of cheap organic raw materials via the activation of S─H and N─H bonds into the value-added S─N/S─S bonds chemicals for industrial rubber production is a promising strategy to realize the atomic economic reaction, during which the kinetic inhibition that is associated with the electron transfer at the electrode/electrolyte interface in traditional direct electrocatalysis can be eliminated to achieve higher performance. In this work, a series of di-copper-substituted phosphotungstatebased foams (PW Cu @CMC) are fabricated with tunable loadings (17 to 44 wt%), which can be successfully applied in indirect electrocatalytic syntheses of sulfenamides and disulfides. Specifically, the optimal PW Cu @CMC (44 wt%) exhibits excellent electrocatalytic performance for the construction of S─N/S─S bonds (yields up to 99%) coupling with the efficient production of H (≈50 µmol g h ). Remarkably, it enables the scale-up production (≈14.4 g in a batch experiment) and the obtained products can serve as rubber vulcanization accelerators with superior properties to traditional industrial rubber additives in real industrial processes. This powerful catalysis system that can simultaneously produce rubber vulcanization accelerator and H may inaugurate a new electrocatalytic avenue to explore polyoxometalate-based foam catalysts in electrocatalysis field.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/adma.202304716 | DOI Listing |
Small
December 2024
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry and Material Science, Northwest University, Xi'an, 710127, China.
Direct formic acid fuel cell (DFAFC) is an efficient power generation device, due to its high energy density, low fuel crossover and low emission. However, the anodic reaction of DFAFC, formic acid oxidation (FAOR), inevitably proceeds through an indirect pathway, adsorbing carbon monoxide intermediate (CO), resulting in a rapid decline of activity for FAOR. Therefore, effectively removing CO is the key to the development of DFAFC.
View Article and Find Full Text PDFJ Environ Sci (China)
June 2025
Environmental Science and Engineering Department, Indian Institute of Technology Bombay, Mumbai-400076, India; Center for Research in Nanotechnology and Science (CRNTS), Indian Institute of Technology Bombay, Mumbai-400076, India; Interdiscliniplary Program in Climate Studies, Indian Institute of Technology Bombay, Mumbai-400076, India; Center of Excellence on Membrane Technologies for Desalination, Brine Management and Water Recycling (DESALTM), Indian Institute of Technology Bombay, Mumbai-400076, India. Electronic address:
J Hazard Mater
November 2024
Key Laboratory of Chemical Pollution Control and Resources Reuse, School of Environmental and Biological Engineering, Nanjing University of Science and Technology, Nanjing 210094, Jiangsu, China. Electronic address:
Anal Chim Acta
November 2024
Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Ubon Ratchathani University, Ubon Ratchathani, 34190, Thailand. Electronic address:
Background: Carcinoembryonic Antigen (CEA) and 4-nitroquinoline-N-oxide (4-NQO) are cancer markers that play a crucial role in tumor risk assessment and early cancer diagnosis. Therefore, it is in demand to develop a fast, accurate, simple, and cost-effective method to detect these cancer markers for quick and early stage-cancer diagnosis and treatment.
Results: Herein, we report a dual signaling approach for direct and indirect signal transduction of cancer biomarker binding on molecularly imprinted-electrodes integrated on an ePAD, enabling sensitive and selective quantitative analysis of 4-NQO and CEA.
J Environ Manage
November 2024
Institut National de la Recherche Scientifique (INRS) - Centre Eau Terre Environnement (ETE), 490 rue de la Couronne, Québec, QC, G1K 9A9, Canada. Electronic address:
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!