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1.
《Arabian Journal of Chemistry》2022,15(10):104139
Pressure oxidation leaching behavior of chalcopyrite in sulfuric acid solution from 110 °C to 150 °C were investigated by in-situ electrochemical methods. Leaching experiments under saturated vapor pressure conditions were used to simulate the anoxic environment that may be encountered in industrial applications. Scanning electron microscope and X-ray photoelectron spectroscopy were used to characterize the morphology and the chemical status of chalcopyrite surface. Results show that the copper extraction was increased with the increase of leaching temperature. Under the optimal leaching conditions under saturated vapor pressure, the copper and iron extraction are 8.3% and 29.8%, respectively. When the temperature increased from 110 °C to 150 °C, the self-corrosion potential and electrochemical reaction resistance firstly increased and then decreased. In contrast, the resistance of the passive film was always increased with the increase of temperature. The electrochemical study results indicated that the increase in temperature affected the oxidation of chalcopyrite by altering the kinetics of the cathodic reaction and the anodic passivation. Both the self-corrosion current density (icorr) and rate constant were affected by the reduction of Fe(III). The XPS results show that elemental sulfur and H3O(Fe3(SO4)2(OH)6) were the main leaching solid products. The formation of H3O(Fe3(SO4)2(OH)6) not only caused a decrease in cathodic reaction kinetics, but also increased the resistance of mass transfer process. Due to the faster release of iron, copper-rich sulphides were formed, which mixed with the elemental sulfur and/or H3O(Fe3(SO4)2(OH)6) led to coverage of the chalcopyrite surface. 相似文献
2.
Wacker oxidation is an industry-adopted process to transform olefins into value-added epoxides and carbonyls. However, traditional Wacker oxidation involves the use of homogeneous palladium and copper catalysts for the olefin addition and reductive elimination. Here, we demonstrated an ultrahigh loading Cu single atom catalyst(14% Cu, mass fraction) for the palladium-free Wacker oxidation of 4-vinylanisole into the corresponding ketone with N-methylhydroxylamine hydrochloride as an additive under mild conditions. Mechanistic studies by 18O and deuterium isotope labelling revealed a hydrogen shift mechanism in this palladium-free process using N-methylhydroxylamine hydrochloride as the oxygen source. The reaction scope can be further extended to Kucherov oxidation. Our study paves the way to replace noble metal catalysts in the traditional homogeneous processes with single atom catalysts. 相似文献
3.
4.
Qi-Jun Li Ya-Jie Ren Qin Xie Min Wu Hua-Xing Feng Li-Mei Zheng Hua-Xin Zhang Jin-Qiao Long Tian-Shun Wang 《应用有机金属化学》2020,34(10):e5813
Two nickel complexes, [Ni(tpen)](ClO4)2.0.5CH3COCH3 ( 1 ) and [Ni(tpbn)](ClO4)2 ( 2 ), of tetrapyridyl ligands N,N,N′,N′-tetrakis(2-pyridyl-methyl)-1,2-ethanediamine (tpen) and N,N,N′,N′-tetrakis(2-pyridyl-methyl)-1,4-butanediamine (tpbn) were prepared and their catalysis for water oxidation reaction (WOR) studied. In 0.1 M phosphate buffer solution (PBS) of pH 8.0, complex 1 is a homogeneous molecular catalyst with an overpotential of ~440 mV and a Faradaic efficiency of 89%. At pH ≥ 9.0, complex 1 degraded gradually during the catalytic process and formed NiOx composite (nickel oxide with general formula NixOyHz) active for WOR. In contrast, complex 2 deteriorated under measured conditions (pH 8.0–12.0) and formed NiOx composite active for WOR. The NiOx composite derived from 1 in 0.1 M PBS at pH 11.0 showed an activity with an overpotential of ~500 mV, a Tafel slope of ~90 mV/decade and a Faradaic efficiency of 97%. Mechanisms were proposed for water oxidation catalyzed by 1 and 2 . This work revealed that the catalytic activity of the nickel complexes was related to the flexibility of the tetrapyridyl ligands and the adaptability of the coordination sphere of the nickel(II) center. 相似文献
5.
For the first time, a novel, straightforward and inexpensive route for immobilization of metals in Schiff base complex form is reported applying 2,4‐toluenediisocyanate as a precursor of primary amine group. A nickel(II) Schiff base complex supported on nano‐TiO2 was designed and synthesized as an effective heterogeneous nanocatalyst for organic reactions, and well characterized using various techniques such as Fourier transform infrared spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, X‐ray diffraction, energy‐dispersive X‐ray analysis and thermogravimetric analysis. The catalytic efficiency of the complex was evaluated in selective oxidation of sulfide to sulfoxide by hydrogen peroxide as an oxidant under solvent‐free conditions at room temperature, which successfully resulted in high yield and high conversion of products. Effective factors including solvent type, oxidant and catalyst amount were also optimized. The catalyst shows outstanding reusability and could be impressively recovered for six consecutive cycles without significant change of its catalytic efficiency. 相似文献
6.
Cytochrome P450 119 Compounds I Formed by Chemical Oxidation and Photooxidation Are the Same Species
Dr. Zhi Su Dr. John H. Horner Prof. Dr. Martin Newcomb 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(61):14015-14020
Compound I from cytochrome P450 119 prepared by the photooxidation method involving peroxynitrite oxidation of the resting enzyme to Compound II followed by photooxidation to Compound I was compared to Compound I generated by m-chloroperoxybenzoic acid (MCPBA) oxidation of the resting enzyme. The two methods gave the same UV/Visible spectra, the same products from oxidations of lauric acid and palmitic acid and their (ω-2,ω-2,ω-3,ω-3)-tetradeuterated analogues, and the same kinetics for oxidations of lauric acid and caprylic acid. The experimental identities between the transients produced by the two methods leave no doubt that the same Compound I species is formed by the two methods. 相似文献
7.
《Arabian Journal of Chemistry》2019,12(5):709-717
In this work a carbon nanotube–Ce-modified PbO2 (CNT–Ce–PbO2) electrode was prepared by electrodeposition method, and compared with pure PbO2, Ce–PbO2, and CNT–PbO2 electrodes. The direct and indirect oxidation capacities of prepared electrodes in electro-catalytic oxidation processes were investigated by cyclic voltammetry and hydroxyl radical production tests, respectively. The electro-catalytic activity of electrodes was examined by electro-catalytic oxidation of a model pollutant of m-nitrophenol (m-NP). Besides, high-performance liquid chromatography (HPLC) was also employed to identify the products resulting from the electro-catalytic oxidation of m-NP and the degradation mechanism of m-NP was proposed. Results show that the CNT–Ce–PbO2 anode has higher direct and indirect oxidation capacities than pure PbO2, Ce–PbO2, and CNT–PbO2 anodes. In the electro-catalytic oxidation of m-NP, the m-NP can be oxidized and degraded at all anodes, and the oxidation reactions of m-NP follow first-order kinetics. m-NP and TOC removal efficiencies are about 0.987 and 0.622 after electrolysis of 120 min and a maximum first-order rate constant of 0.036 min−1 is achieved at the CNT–Ce–PbO2 anode, which are obviously higher than those of the other three kinds of anodes. 相似文献
8.
The first-principles DFT calculations together with microkinetic analysis reveal the complex catalytic mechanism of low-content NO oxidation on CrO2(110) at room temperature. It quantitatively makes clear that CrO2(110) can exhibit considerable activity with the Mars-van-Krevelen mechanism preferred, and the nitrate species serves as the key poisoning species. 相似文献
9.
Masaharu Ueno Satoshi D. Ohmura Makoto Wada Norikazu Miyoshi 《Tetrahedron letters》2019,60(7):570-573
We developed an environmentally friendly method for aerobic oxidation of alcohols using a commercially available, relatively benign bismuth salt as a catalyst. We found that the catalytic combination of BiBr3 with nitric acid is key for enhancing the reactivity. The reaction proceeds well under air, making the use of pure oxygen unnecessary. Each of the primary or secondary alcohols tested was oxidized to the corresponding aldehydes or ketones using this protocol. 相似文献
10.
SiO负载Au-Pd双金属纳米颗粒催化甲醇选择性氧化合成甲酸甲酯 《燃料化学学报》2019,47(7):780-790
甲醇选择氧化制备甲酸甲酯(MF)是延伸甲醇产业链、开发高附加值下游产品的有效途径之一,负载型Au及Pd催化剂在这一反应中表现出优异的低温催化性能。为探索实用、高效和易再生的甲醇选择氧化催化剂,同时揭示双金属颗粒中Au和Pd的协同效应及甲醇氧化反应机理,本研究制备了一系列二氧化硅负载的Au-Pd催化剂(Au-Pd/SiO2),详细研究了其对甲醇选择氧化制甲酸甲酯的催化性能。结果表明,Au和Pd总负载量为0.6%、且Au/Pd质量比为2时,所制备的Au2-Pd1/SiO2催化剂表现出优异的甲醇氧化催化性能;在130℃下,甲醇转化率达到57.0%,MF选择性为72.7%。多种表征结果显示,Au-Pd双金属纳米颗粒粒径为2-4 nm,高度分散于SiO2载体表面,倾向于生成孪晶结构并暴露(111)晶面,这些因素是Au-Pd/SiO2具有优异催化性能的主要原因。通过DRIFTS表征研究,提出了一个可能的MF生成机理:即甲醇首先与处于Au-Pd纳米粒子界面的表面氧作用,生成化学吸附的甲氧基;随后,甲氧基经去质子作用生成吸附的甲醛物种,后者与相邻的甲氧基物种亲核反应,并经β-H消除后得到目标产物MF。 相似文献