A micropolar mixture theory of multi-component porous media

A mixture theory is developed for multi-component micropolar porous media with a combination of the hybrid mixture theory and the micropolar continuum theory. The system is modeled as multi-component micropolar elastic solids saturated with multi- component micropolar viscous fluids. Balance equations are given through the mixture theory. Constitutive equations are developed based on the second law of thermodynamics and constitutive assumptions. Taking account of compressibility of solid phases, the volume fraction of fluid as an independent state variable is introduced in the free energy function, and the dynamic compatibility condition is obtained to restrict the change of pressure difference on the solid-fluid interface. The constructed constitutive equations are used to close the field equations. The linear field equations are obtained using a linearization procedure, and the micropolar thermo-hydro-mechanical component transport model is established. This model can be applied to practical problems, such as contaminant, drug, and pesticide transport. When the proposed model is supposed to be porous media, and both fluid and solid are single-component, it will almost agree with Eringen＇s model.     

Multi-component Dirac equation hierarchy and its multi-component integrable couplings system

A general scheme for generating a multi-component integrable equation hierarchy is proposed. A simple 3M-dimensional loop algebra \tilde{X} is produced. By taking advantage of \tilde{X}, a new isospectral problem is established and then by making use of the Tu scheme the multi-component Dirac equation hierarchy is obtained. Finally, an expanding loop algebra \tilde{F}_M of the loop algebra \tilde{X} is presented. Based on the \tilde{F}_M, the multi-component integrable coupling system of the multi-component Dirac equation hierarchy is investigated. The method in this paper can be applied to other nonlinear evolution equation hierarchies.     

面向任务保障的多组件系统效益优化策略

为了保障系统在执行任务期间高可靠、高效益的运行,从系统效益的角度出发,构建了系统可靠性模型,采用边际效应思想构建了效益重要度,提出了一种面向任务保障的多组件系统效益优化策略。当系统可靠度下降到设定阈值时,计算系统各组件的效益重要度,选择效益重要度最大的组件进行备件分配,如此进行迭代,直到完成任务保障,形成最优的备件分配序列。通过该策略实现了以运行效益最优为目标,以系统可靠度和任务保障时长为约束的备件分配序列。最后,通过数值仿真验证了该策略的可行性。     

A Switchable Catalyst Duo for Acyl Transfer Proximity Catalysis and Regulation of Substrate Selectivity

Enzymes are encoded with a gamut of information to catalyze a highly selective transformation by selecting the proper reactants from an intricate mixture of constituents. Mimicking biological machinery, two switchable catalysts with differently sized cavities and allosteric control are conceived that allow complementary size-selective acyl transfer in an on/off manner by modulating the effective local concentration of the substrates. Selective activation of one of two catalysts in a mixture of reactants of similar reactivity enabled upregulation of the desired product.     

2-取代-4(3H)-喹唑啉酮在Br(o)nsted酸性功能化离子液体中的微波合成

以N-甲基咪唑、吡啶为起始原料,合成了二种新型Br(o)nsted酸性功能化离子液体:1-(4-磺酸基)苄基-3-甲基咪唑硫酸氢根盐(3a),N-(4-磺酸基)苄基吡啶硫酸氢根盐(3b),以其作为反应介质与催化剂,研究了2-取代-4(3H)-喹唑啉酮的三组分、一锅法微波合成.结果表明,当n(2-氨基苯甲酸):n(酰氯):n(乙酸铵):n(3a或3b)=1:1.2:1.5:0.1时,反应6 min即可完成,产率81%～95%.离子液体经减压蒸馏、真空干燥可重复使用3次,催化活性基本保持不变.     

2-取代-4(3H)-喹唑啉酮在BrФnsted酸性功能化离子液体中的微波合成

以N-甲基咪唑、吡啶为起始原料,合成了二种新型BrФnsted酸性功能化离子液体:1-(4-磺酸基)苄基-3-甲基咪唑硫酸氢根盐(3a),N-(4-磺酸基)苄基吡啶硫酸氢根盐(3b),以其作为反应介质与催化剂,研究了2-取代-4(3H)-喹唑啉酮的三组分、一锅法微波合成.结果表明,当n(2-氨基苯甲酸):n(酰氯):n(乙酸铵):n(3a或3b)=1:1.2:1.5:0.1时,反应6min即可完成,产率81%～95%.离子液体经减压蒸馏、真空干燥可重复使用3次,催化活性基本保持不变.     

Heteropoly acid supported on activated natural clay-catalyzed synthesis of 3,4-dihydropyrimidinones/thiones through Biginelli reaction under solvent-free conditions

Dihydropyrimidinones/thiones (DHPM’s) have been prepared by one-pot condensation of methyl acetoacetate, aldehydes, urea/thiourea in the presence of heteropoly-11-tungsto-1-vanadophosphoric acid, H₄[PVW₁₁O₄₀]?·?32H₂O, (HPV) supported on activated natural clay (HPVAC) under solvent-free reaction condition have been proposed. The DHPM derivatives were identified through elemental analysis and melting point measurements and characterized by FT-IR, ¹H-NMR, ¹³C-NMR spectroscopic methods.     

Bismuth triflate：A highly efficient catalyst for the synthesis of bio-active coumarin compoundsvia one-pot multi-component reaction

A series of coumarin-chalcone hybrid compounds and coumarins linked to pyrazoline was synthe-sized in good yield and short time using a simple and efficient method. This method involved the one-pot reaction of salicylaldehyde, an α-ketoester and an aromatic aldehyde (in the case of the coumarin-chalcone derivatives) in addition to hydrazine hydrate (in the case of the pyrazolyl cou-marins) in the presence of a catalytic amount of bismuth triflate [Bi(OTf)3, 5 mol%]. The synthesized compounds showed scavenging activity towards the free radical 2,2-diphenyl-1-picrylhydrazyl. All compounds were characterized using IR,1H NMR and13C NMR spectroscopy.     

An efficient synthesis of benzylidene-2-alkoxy-4-aryl-2,3-cycloalkenopyridine-3-carbonitrile derivatives

An efficient procedure for the synthesis of a novel class of benzylidene-2-alkoxy-4-aryl-6,7-dihydro-5H-cyclopenta[b]pyridine-, -5,6,7,8-tetrahydroquinoline and/or -6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridine-3-carbonitrile was introduced through the one-pot multi-component reaction of cyclopentanone, cyclohexanone, and/or cycloheptanone with different aromatic aldehydes and malononitrile. The same products were also produced by classical route by the two-component reaction of dibenzylidine cyclopentanone, cyclohexanone, and/or cycloheptanone derivatives with malononitrile. The reactions were achieved using sodium alkoxide solution as catalyst and reagent.     

Microwave-Promoted Facile and Rapid Synthesis Procedure for the Efficient Synthesis of 5,5-Disubstituted Hydantoins

A fast, general, environmentally friendly, and facile method for preparation of 5, 5-disubstituted hydantoins from the reaction between ketone (or aldehyde) derivatives with KCN and ammonium carbonate under microwave irradiation is presented. The microwaves remarkably accelerated this reaction, the reaction times decreased dramatically, the reaction conditions were milder, and the yields were also greater. Also a comparative study of microwave versus classical conditions has been done. All the products were characterized by infrared, NMR, and CHN analysis, and their melting points are identical to those of the known compounds reported in the literature. This method might be useful in the future for the preparation of similar derivatives.

[Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications® for the following free supplemental resources: Full experimental and spectral details.]