SCR activity of Cu-SAPO-34 catalyst was reduced by alkali metal ions. The alkali metals ions (Li, Na and K) have shown irregular influences on Cu-SAPO-34. The order of poisoning strengths under 400 °C was found to be: Na > K > Li, which is not consistent with the basicities of their corresponding metals. Experimental results and calculations showed that the alkali metal ions readily replace H and Cu/Cu ions. These exchanges result in the loss of Brønsted acid sites and migration of isolated Cu ions in Cu-SAPO-34, which decrease the NH-SCR activity. Both the basicity and ion diameter will affect the exchanging behavior of an alkali ion. Na and Li ions will influence both H and Cu/Cu ions but K ions only preferably replace the H. We hypothesize that K cannot enter into a small ring (6-membered ring) to replace a Cu/Cu ion because of its large ion diameter. The displaced Cu/Cu ions will transfer to adjacent unbonded Al site to form a CuAlO species.
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http://dx.doi.org/10.1016/j.jhazmat.2019.122007 | DOI Listing |
Adv Mater
January 2025
State Key Laboratory of Petroleum Molecular & Process Engineering, Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai, 200062, China.
Copper-based electrocatalysts are recognized as crucial catalysts for CO electroreduction into multi-carbon products. However, achieving copper-based electrocatalysts with adjustable valences via one-step facile synthesis remains a challenge. In this study, Cu/CuO heterostructure is constructed by adjusting the anion species of the Cu ions-containing electrolyte during electrodeposition synthesis.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Chemistry, Biochemistry and Pharmaceutical Sciences, University of Bern, 3012 Bern, Switzerland.
Binuclear silver(I) and copper(I) complexes, and , with bridging diphenylphosphine ligands were prepared. In , the silver(I) center is located inside a trigonal plane composed of three phosphorus donors from three separate and bridging dppm ligands. The fourth coordination site is filled with neighboring silver(I) ions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Institute of Materials Research, Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China.
Vanadium flow battery (VFB) promises a route for achieving grid-scale power storage by harnessing renewable energy sources. However, the sluggish reaction kinetics of vanadium redox couples and serious hydrogen evolution reaction (HER) still restrict the further development of VFB. Addressing these challenges requires not only effective solutions but also ones that are cost-efficient and scalable to meet the demands of affordable energy storage.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Anhui Provincial Key Laboratory of Magnetic Functional Materials and Devices, School of Materials Science and Engineering, Anhui University, 111 Jiulong Road, Hefei 230601, Anhui, China.
The electrocatalytic reduction of CO to multicarbon (C) products is of great importance but still faces challenges. The moderate oxidation state of Cu (Cu) plays a critical role in promoting the C-C coupling, thereby enhancing the Faraday efficiency (FE) for C products. However, Cu active species are unstable during the reaction.
View Article and Find Full Text PDFActa Crystallogr B Struct Sci Cryst Eng Mater
December 2024
School of Chemistry, University College Dublin, Belfield, Dublin 4, D04 N2E5, Ireland.
Hydrothermal synthesis led to four novel 3D pillared-layer metal-organic frameworks: [Cu(4,4'-bipy)(MoO)·0.3HO] (1), [Cu(4,4'-bipy)(MoO)·0.25HO] (2), [Cu(4,4'-bipy)(MoO)·0.
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