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The increasing demand for sustainable and efficient energy storage materials has led to significant research into utilizing waste biomass for producing activated carbons. This study investigates the impact of the structural properties of activated carbons derived from various lignocellulosic biomasses-barley straw, wheat straw, and wheat bran-on the electrochemical performance of supercapacitors. The Fourier Transform Infrared (FTIR) spectroscopy analysis reveals the presence of key functional groups and their transformations during carbonization and activation processes.

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Hydrolytic dehydrogenation of ammonia borane is a significant and promising approach for on-site hydrogen production at ambient conditions, and developing highly efficient and low-cost catalysts has attracted considerable attention. Herein, waste-biomass-derived activated carbon (AC) was prepared by hydrothermal carbonization and alkali-assisted activation, and non-precious bimetal phosphides (Co-Cu-P) nanocatalysts with a series of different Co/Cu ratios were synthesized on the AC surface through phosphidation method. Owing to the synergetic effects, the optimal CoCuP/AC presents an outstanding turnover frequency of 26.

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A regenerable N-rich hierarchical porous carbon synthesized from waste biomass for HS removal at room temperature.

Sci Total Environ

May 2021

College of Architecture and Environment, Sichuan University, Chengdu 610065, PR China; National Engineering Research Center for Flue Gas Desulfurization, Sichuan University, Chengdu 610065, PR China.

In this study, N-rich hierarchical porous carbons (NPCs) were synthesized via one step strategy from cypress sawdust with carbon nitride (CN) loading and KCO activation. NPCs exhibited excellent performance for HS removal with the sulfur capacity up to 426.2 mg/g at room temperature.

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One-step production of long-chain hydrocarbons from waste-biomass-derived chemicals using bi-functional heterogeneous catalysts.

Phys Chem Chem Phys

February 2014

Center of Economic Excellence for Strategic Approaches to the Generation of Electricity and Department of Chemical Engineering, University of South Carolina, Columbia, SC 29208, USA.

In this study, we demonstrate the production of long-chain hydrocarbons (C8+) from 2-methylfuran (2MF) and butanal in a single step reactive process by utilizing a bi-functional catalyst with both acid and metallic sites. Our approach utilizes a solid acid for the hydroalkylation function and as a support as well as a transition metal as hydrodeoxygenation catalyst. A series of solid acids was screened, among which MCM-41 demonstrated the best combination of activity and stability.

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