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Ling Zhang Hongqi Wan Lei Chen Huidi Zhou Jianmin Chen 《Journal of Dispersion Science and Technology》2013,34(6):846-850
Sb2S3 nanoparticles surface-modified with S-tetradecyl N, N-dihydroxyethyl dithiocarbamate (C14DTC-Sb2S3) have been synthesized via extraction of Sb2S3 colloidal particles from ethylene glycol into toluene in the presence of C14DTC. The obtained products were characterized by high-resolution transmission electron microscope (HRTEM) and Fourier transformation infrared (FTIR), and their tribological behaviors as an additive in liquid paraffin were investigated using a four-ball tribometer. The results show that C14DTC-Sb2S3 nanoparticles can significantly improve the friction reduction, anti-wear, and load-carrying properties of base oils. The preliminary lubrication mechanism was discussed based on the SEM and XPS investigation of the rubbed surfaces. 相似文献
54.
Biswanath Das Penagaluri Balasubramanyam Maddeboina Krishnaiah Boyapati Veeranjaneyulu Dega Sudhakar 《合成通讯》2013,43(14):2113-2121
Regio-, stereo-, and chemoselective ring opening of epoxides with thiols using Cu/MgO as a heterogeneous catalyst has efficiently been carried out to produce the corresponding β-hydroxy sulfides in excellent yields at room temperature under solvent-free conditions. The treatment of the epoxides with thiols and 50% aqueous H2O2 in the presence of the same catalyst at room temperature affords the β-hydroxy sulfoxides in excellent yields. 相似文献
55.
Qian‐Lin Tang 《International journal of quantum chemistry》2013,113(16):1992-2001
Practical copper (Cu)‐based catalysts for the water–gas shift (WGS) reaction was long believed to expose a large proportion of Cu(110) planes. In this work, as an important first step toward addressing sulfur poisoning of these catalysts, the detailed mechanism for the splitting of hydrogen sulfide (H2S) on the open Cu(110) facet has been investigated in the framework of periodic, self‐consistent density functional theory (DFT‐GGA). The microkinetic model based on the first‐principles calculations has also been developed to quantitatively evaluate the two considered decomposition routes for yielding surface atomic sulfur (S*): (1) H2S → H2S* → SH* → S* and (2) 2H2S → 2H2S* → 2SH* → S* + H2S* → S* + H2S. The first pathway proceeding through unimolecular SH* dissociation was identified to be feasible, whereas the second pathway involving bimolecular SH* disproportionation made no contribution to S* formation. The molecular adsorption of H2S is the slowest elementary step of its full decomposition, being related with the large entropy term of the gas‐phase reactant under realistic reaction conditions. A comparison of thermodynamic and kinetic reactivity between the substrate and the close‐packed Cu(111) surface further shows that a loosely packed facet can promote the S* formation from H2S on Cu, thus revealing that the reaction process is structure sensitive. The present DFT and microkinetic modeling results provide a reasonably complete picture for the chemistry of H2S on the Cu(110) surface, which is a necessary basis for the design of new sulfur‐tolerant WGS catalysts. © 2013 Wiley Periodicals, Inc. 相似文献
56.
Yanjun Wang Shaoyun Chen Heng Chen Xingzhou Yuan Yongchun Zhang 《Journal of Energy Chemistry》2013,22(6):902-906
Removal of carbonyl sulfide (COS) from CO2 stream is significant for the production and utilization of food grade CO2. This study investigates the adsorption performance of Ag/NaZSM-5 as adsorbent prepared by incipient wetness impregnation for the removal of COS from a CO2 stream in a fixed-bed adsorption apparatus. Effects of various conditions on the preparation of adsorbent, adsorption and desorption were intensively examined. The results revealed that COS can be removed to below 1×10?9 from a CO2 stream (1000 ppm COS/CO2) using Ag/NaZSM-5 (10 wt% AgNO3) with an adsorption capacity of 12.86 mg-g?1. The adsorbent can be fully regenerated using hot air at 450 °C. The adsorption ability remained stable even after eight cycles of regeneration. 相似文献
57.
The Carbon sphere@Nickel sulfide core-shell nanocomposites for different mole ratios of Carbon sphere (0:1; 0.5:1 and 1:1) have been synthesized by a facile low temperature water-bath method without any further calcination. XRD studies on the core-shell nanocomposites show that characteristic peaks associated with rhombohedral phase structure of nickel sulfide have been retained. TEM morphology presents the interlinked core-shell of Carbon sphere@Nickel sulfide composite with grass-leaf dexterity for better ionic diffusion. BET study confirms the formation of mesoporous structure with high surface area. The existence of elements and its electronic configuration is noted through XPS. The electrochemical studies on pristine nickel sulfide and its Carbon sphere@Nickel sulfide core-shell composites reveal that Carbon sphere@Nickel sulfide (0.5:1) exhibits high specific capacitance of 1022?F?g?1 at a current density of 1?A?g?1. It shows good cyclic performance even beyond 4000 consecutive charge/discharge cycles at a relatively high current density of 20?A?g?1 with the ~83% of retention. 相似文献
58.
Oxidation of methyl ethyl sulfide (CH3SCH2CH3, methylthioethane, MES) under atmospheric and combustion conditions is initiated by hydroxyl radicals, MES radicals, generated after loss of a H atom via OH abstraction, will further react with O2 to form chemically activated and stabilized peroxyl radical adducts. The kinetics of the chemically activated reaction between the CH3SCH2CH2• radical and molecular oxygen are analyzed using quantum Rice-Ramsperger-Kassel theory for k(E) with master equation analysis and a modified strong-collision approach to account for further reactions and collisional deactivation. Thermodynamic properties of reactants, products, and transition states are determined by the B3LYP/6-31+G(2d,p), M062X/6-311+G(2d,p), ωB97XD/6-311+G(2d,p) density functional theory, and CBS-QB3, G3MP2B3, and G4 composite methods. The reaction of CH3SCH2CH2• with O2 forms an energized peroxy adduct CH3SCH2CH2OO• with a calculated well depth of 34.1 kcal mol−1 at the CBS-QB3 level of theory. Thermochemical properties of reactants, transition states, and products obtained under CBS-QB3 level are used for calculation of kinetic parameters. Reaction enthalpies are compared between the methods. The temperature and pressure-dependent rate coefficients for both the chemically activated reactions of the energized adduct and the thermally activated reactions of the stabilized adducts are presented. Stabilization and isomerization of the CH3SCH2CH2OO• adduct are important under high pressure and low temperature. At higher temperatures and atmospheric pressure, the chemically activated peroxy adduct reacts to new products before stabilization. Addition of the peroxyl oxygen radical to the sulfur atom followed by sulfur-oxygen double bond formation and elimination of the methyl radical to form S(= O)CCO• + CH3 (branching) is a potentially important new pathway for other alkyl-sulfide peroxy radical systems under thermal or combustion conditions. 相似文献
59.
N-heterocyclic carbenes (NHCs) have been utilized as Brønsted base to catalyze the hydrothiolation reaction between alkynes and thiols to produce the vinyl sulfides stereoselectively. 相似文献
60.
Xuanwei Wang Jianfeng Chen Qiuyun Li Prof. Lingyun Li Prof. Zanyong Zhuang Dr. Fei-Fei Chen Prof. Yan Yu 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(11):3786-3792
Photocatalytic syngas (CO and H2) production with CO2 as gas source not only ameliorates greenhouse effect, but also produces valuable chemical feedstocks. However, traditional photocatalytic systems require noble metal or suffers from low yield. Here, we demonstrate that S vacancies ZnIn2S4 (VS-ZnIn2S4) nanosheets are an ideal photocatalyst to drive CO2 reduction into syngas. It is found that building S vacancies can endow ZnIn2S4 with stronger photoabsorption, efficient electron–hole separation, and larger CO2 adsorption, finally promoting both hydrogen evolution reaction (HER) and CO2 reduction reaction (CO2RR). The syngas yield of CO and H2 is therefore significantly increased. In contrast to pristine ZnIn2S4, the syngas yield over VS-ZnIn2S4 can be improved by roughly ≈4.73 times and the CO/H2 ratio is modified from 1:4.18 to 1:1. Total amount of syngas after 12 h photocatalysis is as high as 63.20 mmol g−1 without use of any noble metals, which is even higher than those of traditional noble metal-based catalysts in the reported literatures. This work demonstrates the critical role of S vacancies in mediating catalytic activity and selectivity, and highlights the attractive ability of defective ZnIn2S4 for light-driven syngas production. 相似文献