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141.
142.
Binhang Yan Pengcheng Xu Xuan Li Cliff Yi Guo Yong Jin Yi Cheng 《Plasma Chemistry and Plasma Processing》2012,32(6):1203-1214
Liquid hydrocarbons including n-hexane, cyclohexane and toluene are pyrolyzed in H2/Ar plasma to investigate the effects of feedstock properties and key operating conditions (e.g., the feedstock specific input power and residence time) on the reaction performance. The experiments verify that the non-aromatic hydrocarbons show better chemical reactivity than partially aromatic substances. Meanwhile, the straight-chain alkanes and cycloalkanes have better yields of ethylene during the pyrolysis. The results also demonstrate that the pyrolysis reactions are almost completed within the first 0.8?ms in Ar/H2 plasma independent of the feed substances (i.e., liquid hydrocarbons), where the increased feedstock specific input power enhances the reactant conversions and correspondingly raises the yields of acetylene. At a feedstock specific input power of 4.7?×?104?kJ/kg, the n-hexane conversion is over 90?% and the yield of acetylene reaches 70?%. In addition, when using n-hexane as the feedstock, very little coke is formed during the course of reaction. Comprehensive comparisons of the current experiments with the data reported in the literature are made to point out the key influencing factors, i.e., the effective mass ratio of C/H (R C/H) in the gaseous phase and the quench temperature. Both two factors would need to be enhanced in order to get a better performance. Finally, the improvements on the specific energy requirement of this process are discussed. 相似文献
143.
This paper considers a multi-stage dynamic hybrid flowshop in which some stage contains several identical batching machines and the other stages contain several identical discrete machines. Each discrete machine can process no more than one operation at a time, and each batching machine can process several jobs continuously in a batch. This problem has a strong practical background in the process industry. Since the problem is NP-hard, improved Lagrangian relaxation (LR) is developed where batch decomposition strategy is applied and mixed backward and forward dynamic programming is designed to solve batch-level subproblems with the case that each operation may have multiple predecessors and successors. Results of numerical experiments with up to 60 jobs show that the proposed algorithm can obtain better solutions in a reasonable computation time than traditional LR. 相似文献
144.
Microchimica Acta - The authors describe a rapid and highly sensitive point-of-care device for rapid determination of noroviruses, a leading cause of acute gastroenteritis. The assay is based on... 相似文献
145.
Li Zhen Gong Wenli Chen Xuan Liu Lin Meng Ranju Ding Yanhong Yao Juming 《Cellulose (London, England)》2021,28(17):11097-11108
Cellulose - Green bio-flocculants from renewable biomass resources have received the widespread attention for wastewater treatment, which are promising alternatives to petroleum-based synthetic... 相似文献
146.
Tianyong Liu Qian Dang Xunhui Zhou Jin Li Zhen Ge Hang Che Prof. Shaobin Tang Prof. Yi Luo Prof. Jun Jiang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(23):6945-6953
Developing the low-cost and efficient single-atom catalysts (SACs) for nitrogen reduction reaction (NRR) is of great importance while remains as a great challenge. The catalytic activity, selectivity and durability are all fundamentally related to the elaborate coordination environment of SACs. Using first-principles calculations, we investigated the SACs with single transition metal (TM) atom supported on defective boron carbide nitride nanotubes (BCNTs) as NRR electrocatalysts. Our results suggest that boron-vacancy defects on BCNTs can strongly immobilize TM atoms with large enough binding energy and high thermal/structural stability. Importantly, the synergistic effect of boron nitride (BN) and carbon domains comes up with the modifications of the charge polarization of single-TM-atom active site and the electronic properties of material, which has been proven to be the essential key to promote N2 adsorption, activation, and reduction. Specifically, six SACs (namely V, Mn, Fe, Mo, Ru, and W atoms embedded into defective BCNTs) can be used as promising candidates for NRR electrocatalysts as their NRR activity is higher than the state-of-the art Ru(0001) catalyst. In particular, single Mo atom supported on defective BCNTs with large tube diameter possesses the highest NRR activity while suppressing the competitive hydrogen evolution reaction, with a low limiting potential of −0.62 V via associative distal path. This work suggests new opportunities for driving NH3 production by carbon-based single-atom electrocatalysts under ambient conditions. 相似文献
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Copper(I) catalyzed radical benzylation and cyclization reaction of tertiary enamides was investigated and 3,3-disubstituted N-Alkyl isoindolin-1-ones were obtained in moderate to good yields. In this reaction, two new C–C bonds were formed in one step with high atom economy. Possible reaction pathway for the formation of the products was also discussed in this paper. 相似文献
150.
Enantioselective Total Synthesis of (+)‐Steenkrotin A and Determination of Its Absolute Configuration
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Saiyong Pan Beiling Gao Jialei Hu Jun Xuan Hujun Xie Prof. Dr. Hanfeng Ding 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(3):959-970
The first enantioselective total synthesis of (+)‐steenkrotin A has been achieved in 18 steps and 4.2 % overall yield. The key features of the strategy entail a Rh‐catalyzed O?H bond insertion followed by an intramolecular carbonyl‐ene reaction, two sequential SmI2‐mediated Ueno–Stork and ketyl–olefin cyclizations, and a cascade intramolecular aldol condensation/vinylogous retro‐aldol/aldol process with inversion of the relative configuration at the C7 position. The absolute configuration of (+)‐steenkrotin A was determined based on the stepwise construction of the stereocenters during the total synthesis. 相似文献