相对论返波管注入锁相的数值模拟

给出了一种基于梯形慢波结构的相对论返波管结构,并采用2.5维全电磁PIC粒子模拟软件对其前端注入锁相进行了模拟研究。注入功率从二极管区注入相对论返波管中,注入功率50 kW,注入比－48.3 dB时,返波管输出的相位抖动在20范围内,并拟合了返波管相位抖动与注入功率之间关系,给出了判断返波管相位抖动大小的经验公式。注入功率提高至120 MW,注入比－14.5 dB时,注入信号对相对论返波管输出的频率实现了牵引。     

奇异值非线性修正的低对比度红外图像实时增强

由于场景中目标与背景的温差相对较小,红外图像会存在对比度低、视觉效果差的问题,针对这一问题,提出一种基于奇异值非线性修正的红外图像对比度实时增强方法。该方法首先对红外图像进行奇异值分解得到其原始奇异值,然后采用一个对数型非线性变换对图像奇异值进行优化,最后根据修正的奇异值重构出对比度增强的红外图像。利用对数型非线性变换修正图像奇异值不仅能够有效拉伸奇异值的动态范围,同时可优化奇异值的变化梯度,使图像的能量信息得到更充分地表达,改善红外图像不良的视觉效果。实验结果表明,该方法较几种对比方法在视觉效果和客观评价方面均具有更优的增强性能;同时体现出良好的实时性,为实现红外图像的实时增强提供了新途径。     

Metabonomics Study of the Hematopoietic Effect of Medicinal Wine Maoji Jiu on a Blood Deficiency Rat Model by Ultra-High-Performance Liquid Chromatography Coupled to Quadrupole Time-of-Flight Mass Spectrometry and a Pattern Recognition Approach

Maoji Jiu (MJ) is a kind of medicinal wine that has been widely used by Chinese people for many years to nourish and promote blood circulation. The purpose of this study was to investigate the hematopoietic effect of MJ on the metabolism of blood deficient rats and to explore the underlying hematopoietic regulation mechanisms. Blood deficiency model rats were induced by subcutaneous injection of N-acetylphenylhydrazine (APH) and intraperitoneal injection of cyclophosphamide (CTX). The plasma metabolic fingerprints of blood deficiency model rats with and without MJ treatment were obtained by using metabonomics based on ultra-high-performance liquid chromatography coupled to quadrupole time-of-flight mass spectrometry (UHPLC–QTOF/MS). Orthogonal partial least squares-discriminant analysis (OPLS–DA) was used to evaluate the hematopoietic effect of MJ and identify potential biomarkers in the plasma of blood deficiency model rats. The levels of white blood cells (WBC), red blood cells (RBC) and hemoglobin (HGB) and the activity of antioxidant capacity showed a recovery trend to the control group after MJ treatment, while the dose of 10 mL/kg showed the best effect. In this study, thirteen potential biomarkers were identified, which were mainly related to seven metabolic pathways, including linoleic acid metabolism, d-glutamine and d-glutamate metabolism, alanine, aspartate and glutamate metabolism, tryptophan metabolism, pyrimidine metabolism, porphyrin and chlorophyll metabolism and arginine biosynthesis. Metabolomics was applied frequently to reflect the physiological and metabolic state of organisms comprehensively, indicating that the rapid plasma metabonomics may be a potentially powerful tool to reveal the efficacy and enriching blood mechanism of MJ.     

Promote the conductivity of solid polymer electrolyte at room temperature by constructing a dual range ionic conduction path

Poly(ethylene oxide)(PEO) is a classic matrix model for solid polymer electrolyte which can not only dissociate lithium-ions(Li+),but also can conduct Li+through segmental motion in long-range.However,the crystal aggregation state of PEO restricts the conduction of Li⁺ especially at room temperature.In this work,an amorphous polymer electrolyte with ethylene oxide(EO) and propylene oxide(PO) block structure(B-PEG@DMC) synthesized by the transesterification is firstly obtained,showing ...     

DEPENDENCE OF DAMPING CHARACTERISTICS OF A BEAM WITH DAMPING RUBBER MAGNETIC POWDER ON RUBBER PROPERTY

A cantilever beam with Damping Material Applying Rubber Magnetic Powder （DRM） has been investigated. Two methods are selected to hold DRM to a vibrating steel beam, one is to attach DRM by the magnetic attractive force （called DRM beam） and the other by adhesive bonding （called AB-DRM beam）. Different from the damping property of AB-DRM beam caused by shear deformation of damping material, the damping property of DRM beam is characterized by the sliding frictional loss together with the internal loss of damping material. The authors established a formulation to predict the damping characteristics of DRM beam, which was validated experimentally. It is found that rubber material loss factor β has a decisive influence on damping improvement of DRM beam versus AB-DRM beam. If β is smaller than the critical value around 0.8255, a valid range of vibratory amplitude always exists in which DRM beam can achieve better damping than AB-DRM beam; conversely, if β is bigger than the critical value, the valid range does not exist when slide occurs. Such results are used to determine the merits and limitations of DRM and develop design guidelines.     

Effect of various surfactants on stability and thermophysical properties of nanofluids

Journal of Thermal Analysis and Calorimetry - The effect of Fe3O4 nanoparticles and carbon nanotubes (CNTs) on the viscosity of a nanofluid is experimentally investigated from 278 to 313 K...     

Initial Corrosion Characteristics of Enamel Coated Carbon Steel in Hot Tap Water

Russian Journal of Electrochemistry - The corrosion behavior of enamel coating on carbon steel was investigated in the tap water at 80°C (i.e., the simulated electric hot water tank...     

Luminescence Switching of Organogold(I) Complexes between Aggregation-induced Phosphorescence Enhancement and Aggregation-caused Quenching by Balancing Auxiliary Ligands around the AuI Center

Attaching AIE-active L1 ([1,1′:2′,1′′:4′′,1′′′-quaterphenyl]-2-yldiphenylphosphane) to AuCl, shortened the distances of P−C bonds to promote electron cloud overlap between Au^I and L1 , affords 1 ( L1 AuCl) with aggregation-induced phosphorescence enhancement (AIPE) activity by ³LMCT transitions. Then substituting the coplanar L2 (9-ethynylanthracene) for the Cl⁻ in 1 providing 2 , switches the luminescence to aggregation-caused quenching (ACQ) activity. Furthermore, we restore the performance from ACQ to AIPE by metathesis reactions to transfer 2 into 1 . It is versatile synthetic strategy of reversible transformation between 1 and 2 that switches the luminescence of organogold(I) between AIPE and ACQ through balancing auxiliary ligands around the given metal.     

Effect of Arylmethylene Substitutions on Molecular Structure,Optoelectronic Properties and Photovoltaic Performance of Dithienocyclopentafluorene-Based Small-Molecule Acceptors

Two dithienocyclopentafluorene-based small-molecule acceptors (SMAs) were developed that feature methylene-functionalized conjugated side chains, to study the effect of arylmethylene substitution and its number on structure, optoelectronic properties and device performance. Results showed that two SMAs have better absorption properties and planarity, lower bandgaps and higher LUMOs compared with the control SMA without conjugated side chains. The synthesized SMAs were tested in polymer solar cells for examples of their applicability. This work argues that the introduction of methylene-functionalized conjugated side chains has great potential in tuning molecular structure, optoelectronic properties, device physics and photovoltaic performance of SMAs.