Filtering-catalytic candles, filled with an annular packed-bed of commercial Ni-catalyst pellets (∼600 g), were successfully tested for in situ syngas cleaning in a fluidized-bed biomass steam gasifier [Fuel Process. Technol.2019, 191, 44-53, DOI: 10.1016/j.fuproc.2019.03.018]. Those tests enabled the macroscopic evaluation of gasification and gas cleaning as a whole, requiring a more specific assessment of the catalyst performance inside the filter candle. To this end, steam reforming tests of tar key compounds (naphthalene and toluene; thiophene in traces to observe sulfur deactivation) were performed with a laboratory-scale packed-bed reactor containing the same catalyst pellets (<7 g). A lumped kinetics was derived, referred to a pseudocomponent representing tars. This was then validated by simulation of the annular catalytic packed bed inside the filter candle, obtaining numerical results in fair agreement with gasifier outputs. As a result, the lab-scale investigation with a small amount of catalyst provides reliable predictions of tar catalytic reforming in industrial-scale filtering-catalytic candles.
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http://dx.doi.org/10.1021/acs.iecr.0c05131 | DOI Listing |
J Am Chem Soc
July 2024
Shenzhen Grubbs Institute and Department of Chemistry, Guangdong Provincial Key Laboratory of Catalysis, Southern University of Science and Technology, Shenzhen 518055, P. R. China.
The catalytic regio- and enantioselective hydrocarboxylation of alkenes with carbon dioxide is a straightforward strategy to construct enantioenriched α-chiral carboxylic acids but remains a big challenge. Herein we report the first example of catalytic highly enantio- and site-selective remote hydrocarboxylation of a wide range of readily available unactivated alkenes with abundant and renewable CO under mild conditions enabled by the SaBOX/Ni catalyst. The key to this success is utilizing the chiral SaBOX ligand, which combines with nickel to simultaneously control both chain-walking and the enantioselectivity of carboxylation.
View Article and Find Full Text PDFAdv Mater
January 2024
College of Physics Science and Technology, and Center for Interdisciplinary Research, Yangzhou University, Yangzhou, 225002, China.
The development of nonprecious metal catalysts to meet the activity-stability balance at industrial-grade large current densities remains a challenge toward practical alkali-water electrolysis. Here, this work develops an orderly nanodendritic nickel (ND-Ni) catalyst that consists of ultrafine nanograins in chain-like conformation, which shows both excellent activity and robust stability for large current density hydrogen evolution reaction (HER) in alkaline media, superior to currently applied Raney nickel (R-Ni) catalyst in commercial alkali-water electrolyzer (AWE). The ND-Ni catalyst featured by a three-dimensional (3D) interconnecting microporous structure endows with high specific surface area and excellent conductivity and hydrophilicity, which together afford superior charge/mass transport favorable to HER kinetics at high current densities.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2023
School of Chemical Engineering and Advanced Materials, The University of Adelaide, 5005, Adelaide, SA, Australia.
A highly selective and durable oxygen evolution reaction (OER) electrocatalyst is the bottleneck for direct seawater splitting because of side reactions primarily caused by chloride ions (Cl ). Most studies about OER catalysts in seawater focus on the repulsion of the Cl to reduce its negative effects. Herein, we demonstrate that the absorption of Cl on the specific site of a popular OER electrocatalyst, nickel-iron layered double hydroxide (NiFe LDH), does not have a significant negative impact; rather, it is beneficial for its activity and stability enhancement in natural seawater.
View Article and Find Full Text PDFNano Lett
July 2023
Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States.
Lithium-sulfur (Li-S) batteries are promising candidates for next-generation energy storage systems due to their high theoretical energy density and the low cost of sulfur. However, slow conversion kinetics between the insulating S and lithium sulfide (LiS) remains as a technical challenge. In this work, we report a catalyst featuring nickel (Ni) single atoms and clusters anchored to a porous hydrogen-substituted graphdiyne support (termed Ni@HGDY), which is incorporated in LiS cathodes.
View Article and Find Full Text PDFRSC Adv
April 2023
Department of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University Hamedan 6517838683 Iran.
In this paper, KIT-6@SMTU@Ni was successfully synthesized a new method of Ni(ii) complex stabilization on modified mesoporous KIT-6, as a novel and green heterogeneous catalyst. The obtained catalyst (KIT-6@SMTU@Ni) was characterized using Fourier transform infrared spectroscopy (FT-IR), Brunauer-Emmett-Teller (BET) calculation, X-ray diffraction (XRD), atomic absorption spectroscopy (AAS), energy-dispersive X-ray spectroscopy (EDS), X-ray mapping, thermogravimetric analysis (TGA) techniques and scanning electron microscopy (SEM). After complete characterization of the catalyst, it was successfully used for the synthesis of 5-substituted 1-tetrazoles and pyranopyrazoles.
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