Fast pyrolysis of corn stovers with ceramic ball heat carriers in a dual concentric rotary cylinder reactor was studied to explore the product yields and characteristics in response to temperature. The reactor was confirmed to successfully scale up to a 25 kg/h pilot plant, with its performance being excellent. The highest bio-oil yield of 48.3 wt% at 500 °C was attained with the char and gas yields being 26.8 and 24.9 wt%. Phenols content was reduced from 22.3% to 18.9% when elevating temperature from 450 until 600 °C, with guaiacols and alkyl phenols being the predominant compounds, while ketones accounted for 15.8-23.0% and their content showed a continuous increase, with hydroxyacetone being the paramount ketonic one. Acetic acid was the dominant acidic compound with its peak content of 9.4% at 500 °C. The char characteristics in response to temperatures were determined for subsequent processing and high value-added utilization.
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http://dx.doi.org/10.1016/j.biortech.2018.05.033 | DOI Listing |
Environ Pollut
January 2025
Department of Plant and Environmental Sciences, Faculty of Life Sciences, University of Copenhagen, Thorvaldsensvej 40, DK-1871 Frederiksberg C, Denmark. Electronic address:
Nitrogen (N) doping of biomass prior pyrolysis has been identified as an effective approach for enhancing biochar catalytic reactivity. However, high-temperature pyrolysis of N-rich biomass may produce N-devoid biochars with high reactivity, calling for attention to the true causes of the reactivity increases and the role of nitrogen. In this study, N-doped wheat straw biochar (N-BC) materials were produced using urea as N dopant and different pyrolysis conditions, and their catalytic reactivity assessed for the reduction of trichloroethylene (TCE) by green rust (GR), a layered Fe(II)Fe(III) hydroxide.
View Article and Find Full Text PDFNanomaterials (Basel)
January 2025
Department of Materials, School of Natural Science, The University of Manchester, Oxford Road, Manchester M13 9PL, UK.
Platinum (Pt)-based heterogeneous catalysts show excellent performance for the electrocatalytic hydrogen evolution reaction (HER); however, the high cost and earth paucity of Pt means that efforts are being directed to reducing Pt usage, whilst maximizing catalytic efficiency. In this work, a two-step laser annealing process was employed to synthesize Pt single-atom catalysts (SACs) on a MOF-derived carbon substrate. The laser irradiation of a metal-organic framework (MOF) film (ZIF67@ZIF8 composite) by rapid scanning of a ns pulsed infrared (IR; 1064 nm) laser across the freeze-dried MOF resulted in a metal-loaded graphitized film.
View Article and Find Full Text PDFPakistani lignite (PLC) was thermally dissolved at 300 °C using isopropanol (IPA) to obtain a soluble portion (SP) and insoluble portion (ISP). Proximate analysis, ultimate analysis, Fourier transform infrared spectrometry (FTIR), thermogravimetric analysis (TG-DTG) and pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) results were compared to explore the influence of the thermal dissolution process on the pyrolysis for PLC and ISP. Results showed that the thermal dissolution process mainly dissolved some light components of low-rank coal, and more phenols, aldehydes, esters and ethers were found in the SP, indicating that low-carbon alcohols can break the ether bridge bond in coal and generate oxygen-containing organic compounds (OCOCs).
View Article and Find Full Text PDFChem Sci
December 2024
Department of Applied Chemistry, School of Engineering, University of Toyama Gofuku 3190 Toyama 930-8555 Japan
Direct conversion of CO with renewable H to produce methanol provides a promising way for CO utilization and H storage. Cu/ZnO catalysts are active, but their activities depend on the preparation methods. Here, we reported a facile mechanical grinding method for the fast synthesis of Cu@zeolitic imidazolate framework-8 (ZIF-8) derived Cu/ZnO catalysts applied in CO hydrogenation to methanol.
View Article and Find Full Text PDFAdv Mater
January 2025
School of Chemical Engineering, The University of Adelaide, Adelaide, SA, 5005, Australia.
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