Conical bubble photoluminescence from rhodamine 6G in 1, 2-propanediol

A modified U-tube conical bubble sonoluminescence device is used to study the conical bubble photoluminescence. The spectra of conical bubble sonoluminescence at different concentrations of rhodamine 6G (Rh6G) solution in 1,2-propanediol have been measured. Results show that the sonoluminescence from the conical bubbles can directly excite Rh6G, which in turn can fluoresce. The light emission of this kind is referred to as conical bubble photoluminescence. The maximum of fluorescence spectral line intensity in the conical bubble photoluminescence has a red shift in relative to that of the standard photo-excited fluorescence, which is due to the higher self-absorption of Rh6G, and the spectral line of conical bubble photoluminescence is broadened in width compared with that of photo-excited fluorescence.     

Two-dimensional coupled vibration and equivalent circuit of longitudinal-longitudinal orthogonal composite vibration direction converter

With the advantages of transmitting energy from multiple directions to one direction and transforming vibration from one source to multiple directions, the two-dimensional vibra?tion direction converter has important applications in power ultrasonic technology. However, for the complexity of using the wave equation to design and analysis the two-dimensional vibration direction converter, a concise equivalent circuit for the converter is investigated. By introducing the two-dimensional mechanical coupling coefficient and the longitudinal force transform coef?ficient, and using the electromechanical analogy principle, the equivalent circuit and resonance frequency equation of the two-dimensional vibration direction converter vibrating in anti-phase and in-phase two-dimensional coupled vibration are deduced. The resonance frequencies of the vibration direction converters of two different materials are calculated by using the proposed frequency equation, which are in agreement with the results from the finite element method and the experimental test. It provides a concise method for the design and applications of such ultrasonic vibration system.     

三维可穿透目标远场声波反演的一种指示器样本方法

提出了用时谐声散射场的远场信息来可视化三维可穿透目标的一种指示器样本方法,它是通过析取一个指示器函数在包含可穿透目标的某个样本区域中的支集来实现这种可视化的,其中,这个指示器函数在可穿透目标的内部和外部有显著不同的取值.这个算法的一个特别吸引人的性质是不需要关于障碍物的任何几何和物理的先验信息,并且只需要散射场在某个有限孔径中若干个入射和测量方向上的远场信息,即可得到可穿透目标的一个很理想的可视化.数值算例保证了这个可视化算法是有效和实用的 关键词： 声散射 反问题 物形反演     

The effect of disulfide bonds on protein folding,unfolding, and misfolding investigated by FT–Raman spectroscopy

Disulfide bond is relevant to many protein folding/unfolding functions and conformational diseases. To elucidate the effects of disulfide bonds on protein folding, unfolding, and misfolding, we performed Fourier transform–Raman measurements on serial chemical‐induced denaturations of bovine serum albumin (BSA). By directly monitoring Raman stretching at S–S (~507 cm⁻¹), S–H (~2566 cm⁻¹), amide I (1655 cm⁻¹ for α‐helix; 1667 cm⁻¹ for β‐sheet structure), and amide III (>1300 cm⁻¹ for α‐helix; 1246 cm⁻¹ for β‐sheet structure), the status of disulfide bonds and secondary structure of BSA at different states were elucidated. Both disulfide bonds and secondary structure (mostly in α‐helix) of BSA appeared relatively stable even when the protein was unfolded by urea solution. However, disulfide bonds were completely reduced and protein secondary structure changed from α‐helix to a relatively β‐sheet dominant when the protein was modified by the mixed solution of urea and dithiothreitol (urea/DTT). Adhering to these structural changes, the protein proceeded to different degrees of polymerization. BSA would aggregate into a high molecular mass (over 700 kDa) of protein ensemble when it was exposed to the mixed urea/DTT solution. An irreversible change in S–S/S–H conversion and secondary structure was responsible for protein misfolding. We demonstrate here that Fourier transform–Raman directly probe S–S/S–H conversion and secondary structural change of BSA at different states, and these results clearly indicate that disulfide bonds and secondary structure of BSA serve as concrete frameworks to stabilize protein structure. As the frameworks collapse, the protein undergoes an irreversible structural change and results in protein misfolding. Copyright © 2016 John Wiley & Sons, Ltd.     

求解二维三温辐射热传导方程组的一种网格自适应方法

在求解二维三温辐射热传导方程组的过程中,设计了一类新的基于Hessian矩阵的网格自适应算法.数值实验结果表明,与现在流行的基于一阶导数或通量的网格自适应技术相比,该算法能够大幅改善系统的能量守恒误差,并具有较高的整体计算效率.     

Monte Carlo calculation of electron spectra produced in water phantoms by 20 keV-1 GeV photons

Abstract

A Monte Carlo calculation for the energy spectra of electrons and positrons produced in infinite and semiinfinite water phantoms by photons ranging in energies from 20 keV to 1 GeV are presented. The dominant processes considered are the photoelectric effect, Auger effect, Compton effect, pair, and triplet production. Bremsstrahlung produced by electrons and positrons with energies greater than 1 MeV is also included. The effect of multiple Compton scattering, not considered in the earlier calculation, for the infinite phantom for photon energies higher than 2 MeV has been incorporated. For a semi-infinite phantom, multiple Compton scattering and backscattering through the top are considered. The results are compared with the earlier calculations for the first-collision spectrum. It is found that the inclusion of multiple Compton scattering significantly increases the average number of electrons/cm³ per photon/cm² at all energies considered whereas bremsstrahlung reduces the number of high energy electrons and produces more low energy electrons in the spectrum.     

银纳米颗粒对聚合物太阳能电池性能的提高

采用水溶性银纳米颗粒附着在反型太阳能电池的电子传输层上,用以提高有机太阳能电池的短路电流。所制备的器件结构为ITO/ZnO/Ag NPs/P3HT(Poly 3-hexylthiophene):PC_[60]BM/MoO₃/Ag。其金属银纳米颗粒的表面等离激元在410 nm处出现了共振吸收峰,半峰全宽约为60 nm。器件的光电流在可见光范围内均有所增加,短路电流相对于标准器件提高了20.2%,光电转化效率相对提高了17.2%。     

Fluorescent Carbon Dots as Cost-Effective and Facile Probes for Caffeic Acid Sensing via a Fluorescence Quenching Process

Caffeic acid (CA), a familiar color stabilizing reagent, has aroused general concern due to its uncontrolled addition, and thus the detection of CA is increasingly important. In our report, the bright carbon dots (CDs) were prepared via hydrothermal treatment with urea and citric acid act as raw material and their characteristics were discussed through X-ray diffraction (XRD), transmission electron microscopy (TEM) and so on. Impressively, the strong emission of the as-prepared CDs (Quantum Yield: 24.3%) decreased sharply upon a full reaction with the added CA. Hence, we first present an improved strategy for determining CA based upon the quenching of the strong emission of CDs. In this strategy, 0.79–100.0 µmol L^??1 caffeic acid could be simply detected, and a detection limit of 0.24 µmol L^??1 was allowed. Additionally, CA in red wine samples can be successfully detected by this method and the exploration of the quenching mechanism of the CA-CDs system was done.     

Stronger Criteria for Nonseparability in n-Partite Quantum States

We investigate the multipartite entanglement in arbitrary dimensional systems, and separability criteria for nonseparability in n-partite quantum states are derived. Examples such as the generalized noisy-W state and the GHZ basis states mixed with white noise are provided to show that our criteria are independent of and stronger than previously reported ones. Our criteria can also be expressed by the elements of the density matrix, which allows a simple and practical evaluation and computation. The experimental implementation of our criteria is also discussed.