Copper-Based Catalysts Confined in Carbon Nanocage Reactors for Condensed Ester Hydrogenation: Tuning Copper Species by Confined SiO2 and Methanol Resistance

Author(s):  
Yaqi Yao ◽  
Xiaoqian Wu ◽  
Bo Chen ◽  
Zhiyu Tu ◽  
Oliver Y. Gutiérrez ◽  
...  
1981 ◽  
Vol 16 (1) ◽  
pp. 45-58 ◽  
Author(s):  
G. Krantzberg ◽  
P.M. Stokes

Abstract An investigation was made of the effects exerted by benthic macroinvertebrate communities on copper speciation in sediments from a lake which is becoming acidified. In laboratory microcosms, benthic macroinvertebrate communities stimulated the flux of copper from sediment to water. The presence of the macro-benthos resulted in a redistribution of physico-chemical copper species within the sediment with a transfer from more strongly complexed forms (HC1 extractable) to adsorbed and cation exchangeable forms (MgCl2 extractable). The role of bio-turbation in copper transformations is discussed.


ACS Nano ◽  
2021 ◽  
Author(s):  
Yanan Zhang ◽  
Dong Yan ◽  
Zefei Liu ◽  
Youwen Ye ◽  
Fei Cheng ◽  
...  

Materials ◽  
2020 ◽  
Vol 13 (21) ◽  
pp. 4885
Author(s):  
Aneta Święs ◽  
Małgorzata Rutkowska ◽  
Andrzej Kowalczyk ◽  
Urbano Díaz ◽  
Antonio E. Palomares ◽  
...  

Ferrierites and their delaminated forms (ITQ-6), containing aluminum or titanium in the zeolite framework, were synthetized and modified with copper by an ion-exchange method. The obtained samples were characterized with respect to their chemical composition (ICP-OES), structure (XRD, UV-Vis DRS), textural parameters (N2-sorption), surface acidity (NH3-TPD), form and reducibility of deposited copper species (UV-Vis DRS and H2-TPR). Ferrierites and delaminated ITQ-6 zeolites modified with copper were studied as catalysts for the selective catalytic oxidation of ammonia to dinitrogen (NH3-SCO). It was shown that aggregated copper oxide species, which were preferentially formed on Ti-zeolites, were catalytically active in direct low-temperature ammonia oxidation to NO, while copper introduced into Al-zeolites was present mainly in the form of monomeric copper cations catalytically active in selective reduction of NO by ammonia to dinitrogen. It was postulated that ammonia oxidation in the presence of the studied catalysts proceeds according to the internal-selective catalytic reduction mechanism (i-SCR) and therefore the suitable ratio between aggregated copper oxide species and monomeric copper cations is necessary to obtain active and selective catalysts for the NH3-SCO process. Cu/Al-ITQ-6 presented the best catalytic properties possibly due to the most optimal ratio of these copper species.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Cong Wang ◽  
Hui Zhang ◽  
Lucille A. Wells ◽  
Tian Liu ◽  
Tingting Meng ◽  
...  

AbstractN-Arylation of NH-sulfoximines represents an appealing approach to access N-aryl sulfoximines, but has not been successfully applied to NH-diaryl sulfoximines. Herein, a copper-catalyzed photoredox dehydrogenative Chan-Lam coupling of free diaryl sulfoximines and arylboronic acids is described. This neutral and ligand-free coupling is initiated by ambient light-induced copper-catalyzed single-electron reduction of NH-sulfoximines. This electron transfer route circumvents the sacrificial oxidant employed in traditional Chan-Lam coupling reactions, increasing the environmental friendliness of this process. Instead, dihydrogen gas forms as a byproduct of this reaction. Mechanistic investigations also reveal a unique autocatalysis process. The C–N coupling products, N-arylated sulfoximines, serve as ligands along with NH-sulfoximine to bind to the copper species, generating the photocatalyst. DFT calculations reveal that both the NH-sulfoximine substrate and the N-aryl product can ligate the copper accounting for the observed autocatalysis. Two energetically viable stepwise pathways were located wherein the copper facilitates hydrogen atom abstraction from the NH-sulfoximine and the ethanol solvent to produce dihydrogen. The protocol described herein represents an appealing alternative strategy to the classic oxidative Chan-Lam reaction, allowing greater substrate generality as well as the elimination of byproduct formation from oxidants.


Author(s):  
Guro Sørli ◽  
Muhammad Mohsin Azim ◽  
Magnus Ronning ◽  
Karina Mathisen

The first successful synthesis of hierarchical CuSAPO-34 (3.9 wt.% Cu) is reported using the polymer Pluronic F127 as mesoporous structure directing agent (SDA). X-ray absorption spectroscopy (XAS) proved single site...


2018 ◽  
Vol 78 (6) ◽  
pp. 1390-1399 ◽  
Author(s):  
Wenshu Li ◽  
Peng Zhou ◽  
Jing Zhang ◽  
Yongli Zhang ◽  
Gucheng Zhang ◽  
...  

Abstract This study investigated the generation of reactive oxygen species (ROS) (O2−•, H2O2, and HO•) by promoting the Cu(II)/Cu(I) redox cycle with certain reducing agents (RAs) in aerobic aqueous solution, and benzoic acid (BA) was employed as indicator for the hydroxyl radical (HO•). Hydroxylamine (HA) can reduce Cu(II) to Cu(I) to induce chain reactions of copper species resulting in the generation of the superoxide radical (O2−•) and hydrogen peroxide (H2O2), and the intermediate Cu(I) can further activate H2O2 via a Fenton-like reaction to produce HO•, creating the remarkable BA degradation. O2 is indispensable, and unprotonated HA is the motive power in the O2/Cu/HA system. Moreover, pH is a crucial factor of the O2/Cu/HA system due to the protonated HA not being able to reduce Cu(II) into Cu(I). The oxidation of HA can be effectively induced by trace amounts of Cu(II), and both a higher HA dosage and a higher Cu(II) dosage can enhance H2O2 generation and BA degradation. In addition, some other RAs that can reduce Cu(II) into Cu(I) could replace HA in the O2/Cu/HA system to induce the generation of these ROS in aerobic aqueous solution.


1992 ◽  
Author(s):  
Kai-Ming Chi ◽  
Janos Farkas ◽  
Toivo T. Kodas ◽  
Mark J. Hampden-Smith
Keyword(s):  

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