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71.
Electric fields are often used to transport fluids (by electroosmosis) and separate charged samples (by electrophoresis) in microfluidic devices. However, there exists inevitable Joule heating when electric currents are passing through electrolyte solutions. Joule heating not only increases the fluid temperature, but also produces temperature gradients in cross-stream and axial directions. These temperature effects make fluid properties non-uniform, and hence alter the applied electric potential field and the flow field. The mass species transport is also influenced. In this paper we develop an analytical model to study Joule heating effects on the transport of heat, electricity, momentum and mass species in capillary-based electrophoresis. Close-form formulae are derived for the temperature, applied electrical potential, velocity, and pressure fields at steady state, and the transient concentration field as well. Also available are the compact formulae for the electric current and the volume flow rate through the capillary. It is shown that, due to the thermal end effect, sharp temperature drops appear close to capillary ends, where sharp rises of electric field are required to meet the current continuity. In order to satisfy the mass continuity, pressure gradients have to be induced along the capillary. The resultant curved fluid velocity profile and the increase of molecular diffusion both contribute to the dispersion of samples. However, Joule heating effects enhance the sample transport velocity, reducing the analysis time in capillary electrophoretic separations. 相似文献
72.
73.
We consider a class of m-point (m > 3) second order boundary value problem (PF\cal{P}_{F}) in a separable Banach space E of the form
W 2, 1E([0, 1])W ^{2, 1}_E([0, 1])-solutions of (PF\cal{P}_{F}) is compact and is a retract in C1E([0, 1])C^1_E([0, 1]). A new existence result of W 2, 1E([0, 1])W ^{2, 1}_E([0, 1])-solutions and a related relaxation problem are also provided, here F is no longer bounded. 相似文献
74.
75.
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
76.
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
77.
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
78.
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
79.
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
80.
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