Fully integrated PDMS/SU-8/quartz microfluidic chip with a novel macroporous poly dimethylsiloxane (PDMS) membrane for isoelectric focusing of proteins using whole-channel imaging detection

A fully integrated polydimethylsiloxane (PDMS)/modified PDMS membrane/SU-8/quartz hybrid chip was developed for protein separation using isoelectric focusing (IEF) mechanism coupled with whole-channel imaging detection (WCID) method. This microfluidic chip integrates three components into one single chip: (i) modified PDMS membranes for separating electrolytes in the reservoirs from the sample in the microchannel and thus reducing pressure disturbance, (ii) SU-8 optical slit to block UV light (below 300?nm) outside the channel aiming to increase detection sensitivity, and (iii) injection and discharge capillaries for continuous operation. Integration of all these components on a single chip is challenging because it requires fabrication techniques for perfect bonding between different materials and is prone to leakage and blockage. This study has addressed all the challenges and presented a fully integrated chip, which is more robust with higher sensitivity than the previously developed IEF chips. This chip was tested by performing protein and pI marker separation. The separation results obtained in this chip were compared with that obtained in commercial cartridges. Side-by-side comparison validated the developed chip and fabrication techniques.     

脉冲不分流进样气相色谱-质谱法分析血浆中的10种镇静催眠药

采用脉冲不分流进样技术建立了血浆中10种镇静催眠药(巴比妥、异戊巴比妥、苯巴比妥、奥沙西泮、地西泮、硝西泮、氯硝西泮、艾司唑仑、阿普唑仑、三唑仑)的气相色谱-质谱(GC-MS)快速定性定量分析方法.血浆样品经0.1 mol/L 氢氧化钠溶液碱化后,用乙酸乙酯萃取;萃取液经氮气吹干,用乙酸乙酯溶解后进行GC-MS分析,所...     

A hybrid trust region algorithm for unconstrained optimization

This paper presents a hybrid trust region algorithm for unconstrained optimization problems. It can be regarded as a combination of ODE-based methods, line search and trust region techniques. A feature of the proposed method is that at each iteration, a system of linear equations is solved only once to obtain a trial step. Further, when the trial step is not accepted, the method performs an inexact line search along it instead of resolving a new linear system. Under reasonable assumptions, the algorithm is proven to be globally and superlinearly convergent. Numerical results are also reported that show the efficiency of this proposed method.     

Facile electrochemical synthesis of hexagonal Cu2O nanotube arrays and their application

Large-scale and highly oriented single-crystalline hexagonal Cu(2)O nanotube arrays have been successfully synthesized using a two-step solution approach, which involves the electrodeposition of oriented Cu(2)O nanorods and a subsequent dissolution technique along the c axis to form a tubular structure. Herein, NH(4)Cl was found to be an effectual additive, and it can successfully realize the dissolution process of Cu(2)O from nanorods to nanotubes. The dissolution mechanism of Cu(2)O from nanorods to nanotubes was illustrated in detail. These prepared Cu(2)O nanotube arrays were characterized by SEM, EDS, XRD, XPS, and TEM. The photoluminescence (PL) spectrum of Cu(2)O nanotube arrays was also measured, and it shows there is a greater fraction of copper or oxygen vacancies in these prepared Cu(2)O nanotubes. Finally, the applications of Cu(2)O nanotube arrays for gas sensors were investigated in this paper.     

Unusual multi-step sequential Au(III)/Au(II) processes of gold(III) quinoxalinoporphyrins in acidic non-aqueous media

The electrochemistry of gold(III) mono- and bis-quinoxalinoporphyrins was examined in CH(2)Cl(2) or PhCN containing 0.1 M tetra-n-butylammonium perchlorate (TBAP) before and after the addition of trifluoroacetic acid to solution. The investigated porphyrins are represented as Au(PQ)PF(6) and Au(QPQ)PF(6), where P is the dianion of the 5,10,15,20-tetrakis(3,5-di-tert-butylphenyl)porphyrin and Q is a quinoxaline group fused to a β,β'-pyrrolic position of the porphyrin macrocycle; in Au(QPQ)PF(6) there is a linear arrangement where the quinoxalines are fused to pyrrolic positions that are opposite each other. The porphyrin without the fused quinoxaline groups, Au(P)PF(6), was also investigated under the same solution conditions. In the absence of acid, all three gold(III) porphyrins undergo a single reversible Au(III)/Au(II) process leading to the formation of a Au(II) porphyrin which can be further reduced at more negative potentials to give stepwise the Au(II) porphyrin π-anion radical and dianion, respectively. However, in the presence of acid, the initial Au(III)/Au(II) processes of Au(PQ)PF(6) and Au(QPQ)PF(6) are followed by an internal electron transfer and protonation to regenerate new Au(III) porphyrins assigned as Au(III)(PQH)(+) and Au(III)(QPQH)(+). Both protonated gold(III) quinoxalinoporphyrins then undergo a second Au(III)/Au(II) process at more negative potentials. The electrogenerated monoprotonated monoquinoxalinoporphyrin, Au(II)(PQH), is then further reduced to its π-anion radical and dianion forms, but this is not the case for the monoprotonated bis-quinoxalinoporphyrin, Au(II)(QPQH), which accepts a second proton and is rapidly converted to Au(III)(HQPQH)(+) before undergoing a third Au(III)/Au(II) process to produce Au(II)(HQPQH) as a final product. Thus, Au(P)PF(6) undergoes one metal-centered reduction while Au(PQ)PF(6) and Au(QPQ)PF(6) exhibit two and three Au(III)/Au(II) processes, respectively. These unusual multistep sequential Au(III)/Au(II) processes were monitored by thin-layer spectroelectrochemistry and a reduction/oxidation mechanism for Au(PQ)PF(6) and Au(QPQ)PF(6) in acidic media is proposed.     

On optimizing edge connectivity of product graphs

This work studies the super edge connectivity and super restricted edge connectivity of direct product graphs, Cartesian product graphs, strong product graphs and lexicographic product graphs. As a result, sufficient conditions for optimizing the edge connectivity and restricted edge connectivity of these graphs are presented.     

Minimal-speed selection of traveling waves to the Lotka–Volterra competition model

In this paper the minimal-speed determinacy of traveling wave fronts of a two-species competition model of diffusive Lotka–Volterra type is investigated. First, a cooperative system is obtained from the classical Lotka–Volterra competition model. Then, we apply the upper-lower solution technique on the cooperative system to study the traveling waves as well as its minimal-speed selection mechanisms: linear or nonlinear. New types of upper and lower solutions are established. Previous results for the linear speed selection are extended, and novel results on both linear and nonlinear selections are derived.     

SiGe HBT大信号等效电路模型

基于SiGe HBT(异质结双极晶体管)的物理模型，建立了描述SiGe HBT的大信号等效电路模型.该等效电路模型考虑了准饱和效应和自热效应等，模型分为本征和非本征两部分，物理意义清晰，拓扑结构相对简单.该模型嵌入了PSPICE软件的DEVEO(器件方程开发包)中.在PSPICE软件资源的支持下，利用该模型对SiGe HBT器件进行了交直流特性模拟分析，模拟结果与理论分析结果相一致，并且与文献报道的结果符合较好. 关键词： SiGe HBT 等效电路模型 PSPICE     

On the integral representation formula for a two‐component elastic composite

The aim of this paper is to derive, in the Hilbert space setting, an integral representation formula for the effective elasticity tensor for a two‐component composite of elastic materials, not necessarily well‐ordered. This integral representation formula implies a relation which links the effective elastic moduli to the N‐point correlation functions of the microstructure. Such relation not only facilitates a powerful scheme for systematic incorporation of microstructural information into bounds on the effective elastic moduli but also provides a theoretical foundation for inverse‐homogenization. The analysis presented in this paper can be generalized to an n‐component composite of elastic materials. The relations developed here can be applied to the inverse‐homogenization for a special class of linear viscoelastic composites. The results will be presented in another paper. Copyright © 2005 John Wiley & Sons, Ltd.