金属熔体近壁面流动剪切模型及其对金属凝固影响的理论研究

本文建立了金属熔体近壁面流动剪切模型, 并分析了流动剪切对金属凝固的影响. 针对A356合金计算结果表明:层流流动的熔体内部剪应力随垂直斜板表面距离的增大而减小, 随着流动长度的增加先急剧下降之后趋于稳定; 紊流流动的熔体所受的剪应力随着垂直倾斜板表面距离的增大先急剧下降之后趋于稳定, 随着流动长度的增加而不断增大; 斜板倾角越大, 斜板上相同位置的熔体层受到的剪应力越大; 熔体垂直斜板表面距离越小, 柱状晶所承受的弯曲应力越大; 斜角越大, 斜板上相同位置的柱状晶的弯曲应力越大; 随着熔体在倾斜板表面流动长度的增加, 在层流阶段, 倾斜板表面柱状晶根部所受的弯曲应力先急剧下降之后趋于平稳, 而在紊流阶段, 弯曲应力是缓慢增加的; 理论分析表明柱状晶在熔体近壁面流动过程受到的最大弯曲应力低于αup -Al晶粒的屈服强度, 所以斜板上熔体流动产生的弯曲力不能将柱状晶折断, 只能将晶粒冲刷游离到熔体中使晶粒增殖, 与实验结果相符合. 所以本模型可以很好地解释熔体近壁面流动过程中的剪切本构关系以及剪应力对凝固组织的影响.     

认知无线电网络中基于抢占式排队论的频谱切换模型

针对认知无线电网络中认知用户广义传输时间的优化问题, 提出了一种基于抢占式续传优先权M/G/m排队理论的频谱切换模型. 在该排队模型中, 为了最小化认知用户广义传输时间, 采用混合排队-并列式服务的排队方式. 在此基础上, 深入分析多个认知用户、多个授权信道、多次频谱切换条件下认知用户信道使用情况, 从而推导出广义传输时间表达式. 最后探讨了该模型下自适应频谱切换策略. 仿真结果表明, 相比于已有的频谱切换模型, 该模型不仅能够更加完整地描述认知用户频谱切换行为, 而且使得认知用户传输时延更小, 广义传输时间更短. 此外, 认知无线电网络允许的认知用户服务强度增加, 能够容纳的认知用户数量增多. 因此, 该模型提升了认知用户频谱切换的性能, 更好地实现了认知用户与授权用户的频谱共享.     

应用干涉云纹测量工艺应力分布

本文就冷胀孔周残余应力分布的测量技术和干涉螺接孔周干涉应力分布的测量技术进行了实验研究。沿着径向将试件切割,以释放欲测的应力,同时用干涉云纹技术测量由于释放应力而引起的附加应变场。文中还就残余应力在循环载荷作用下的松弛问题进行了实验研究。提供了典型的实验结果,讨论了引起实验误差的主要原因。     

Multiplication operator on the weighted Bergman space of the unit ball北大核心CSCD

Multiplication operator is an important class of operators in function space. We mainly research the properties of the multiplication operator on the weighted Bergman space of the unit ball. ©, 2015, Chinese Academy of Sciences. All right reserved.     

Raman endoscopy for in vivo differentiation between benign and malignant ulcers in the stomach

The aim of this study was to evaluate the clinical utility of an image-guided Raman endoscopy technique for in vivo differential diagnosis of benign and malignant ulcerous lesions in the stomach. A rapid-acquisition image-guided Raman endoscopy system with 785 nm laser excitation has been developed to acquire in vivo gastric tissue Raman spectra within 0.5 s during clinical gastroscopic examinations. A total of 1102 in vivo Raman spectra were acquired from 71 gastric patients, in which 924 Raman spectra were from normal tissue, 111 Raman spectra were from benign ulcers whereas 67 Raman spectra were from ulcerated adenocarcinoma. There were distinctive spectral differences in Raman spectra among normal mucosa, benign ulcers and malignant ulcers, particularly in the spectral ranges of 800-900, 1000-1100, 1245-1335, 1440-1450 and 1500-1800 cm(-1), which primarily contain signals related to proteins, DNA, lipids and blood. The malignant ulcerous lesions showed Raman signals to be mainly associated with abnormal nuclear activity and decrease in lipids as compared to benign ulcers. Partial least squares-discriminant analysis (PLS-DA) was employed to generate multi-class diagnostic algorithms for classification of Raman spectra of different gastric tissue types. The PLS-DA algorithms together with leave-one tissue site-out, cross validation technique yielded diagnostic sensitivities of 90.8%, 84.7%, 82.1%, and specificities of 93.8%, 94.5%, 95.3%, respectively, for classification of normal mucosa, benign and malignant ulcerous lesions in the stomach. This work demonstrates that image-guided Raman endoscopy technique associated with PLS-DA diagnostic algorithms has for the first time promising clinical potential for rapid, in vivo diagnosis and detection of malignant ulcerous gastric lesions at the molecular level.     

Synthesis and characterization of poly(aryl ether ketone) ionomers with sulfonic acid groups on pendant aliphatic chains for proton-exchange membrane fuel cells

A series of parent poly(aryl ether ketone)s bearing different content of unsaturated pendant propenyl groups were synthesized via nucleophilic substitution polymerization from 3,3′-diallyl-4,4′-dihydroxybiphenyl, 9,9′-bis(4-hydroxyphenyl) fluorene and 4,4′-difluorobenzophenone. The polymers with pendant aliphatic sulfonic acid groups were further synthesized by free radical thiol-ene coupling reactions between 3-mercapto-1-propanesulfonic sodium and the parent propenyl functional copolymers. The resulting sulfonated polymers with high inherent viscosity (1.83-4.69 dL/g) were soluble in polar organic solvents and can form flexible and transparent membranes by casting from their solutions. The copolymers with different ion exchange capacity could be conveniently synthesized by varying the monomers ratios. Transmission electron microscopy (TEM) was used to examine the microstructures of the membrane and the results revealed that significant hydrophilic/hydrophobic microphase separation with spherical, uniform-sized (5-10 nm) and well-dispersed hydrophilic domains was afforded. The proton conductivities of the as-prepared membranes and the state-of-the-art Nafion 117 membrane in fully hydrated state were investigated. The results revealed that the proton conductivity of the synthesized membranes increased more remarkably than that of Nafion 117 membrane with increasing temperature. The membrane with 1.69 mequiv/g of IEC had a conductivity of 2.5 × 10⁻² Scm⁻¹ at 100 °C. The membranes also possessed excellent mechanical properties, good thermal, oxidative, hydrolytic and dimensional stabilities.     

A novel label-free electrochemical aptasensor for thrombin based on the {nano-Au/thionine}n multilayer films as redox probes

Herein, a novel label-free electrochemical aptasensor based on direct immobilization of the redox probes on an electrode surface was reported. Gold electrode coated Nafion was firstly modified with redox probe-thionine (Thi) through ion exchange adsorption. Then, with the help of chemisorption and electrostatic adsorption, negatively charged nano-Au and positively charged Thi were layer-by-layer (LBL) self-assembled onto the modified electrode surface, which formed {nano-Au/Thi⁺}_n multilayer films for improving the amount of redox probes and immobilizing thiolated thrombin aptamers (TBA). In the presence of target thrombin (TB), the TBA on the multilayer film could catch the TB onto the electrode surface, which resulted in a barrier for electro-transfer, leading to decrease of the current. The proposed method avoided the cubsome redox probe labeling process, increased the amount of redox probe and reduced the distance between the redox probe and electrode surface. Thus, the approach showed a high sensitivity and a wider linearity to TB in the range from 0.12 nM to 46 nM with a detection limit of 40 pM.     

Liquid–liquid equilibria of ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate and sodium citrate/tartrate/acetate aqueous two-phase systems at 298.15 K: Experiment and correlation

Binodal curves of the aqueous 1-butyl-3-methylimidazolium tetrafluoroborate ([Bmim]BF₄) + sodium citrate (Na₃C₆H₅O₇), [Bmim]BF₄ + sodium tartrate (Na₂C₄H₄O₆) and [Bmim]BF₄ + sodium acetate (NaC₂H₃O₂) systems have been determined experimentally at 298.15 K. The Merchuk equation was used to correlate the binodal data. The effective excluded volume (EEV) values obtained from the binodal model for these three systems were determined. The binodal curves and EEV both indicate that the salting-out abilities of the three salts follow the order: Na₃C₆H₅O₇ > Na₂C₄H₄O₆ > NaC₂H₃O₂. The liquid–liquid equilibrium (LLE) data were obtained by density determination and binodal curves correlation of these systems. Othmer–Tobias and Bancraft, and Setschenow equations were used for the correlation of the tie-line data. Good agreement was obtained with the experimental tie-line data with both models.     

Simultaneous Determination of Testosterone and Testosterone Enanthate in Equine Plasma by UHPLC-MS-MS

Testosterone and testosterone enanthate are performance-enhancing substances that are banned in racehorses competing in the State of Pennsylvania (PA). A tolerance concentration of 2,000 pg mL^?1 plasma has been established for testosterone in intact colts and stallions at the time they are competing in PA. Testosterone enanthate is a precursor of testosterone and can be used to boost plasma testosterone concentration above natural, age and seasonally variable plasma concentration. To control abuse, a verifiable method for rapid determination of both substances in equine plasma was needed. For this reason, an ultra high performance liquid chromatography-tandem mass spectrometry method for high-throughput analysis of both analytes in equine plasma was developed. Analytes were recovered from plasma by liquid–liquid extraction using mixture of methyl tert-butyl ether and ethyl acetate (50:50, v/v), separated on a C₁₈ sub-2 μm column and detected on a triple quadrupole mass spectrometer using positive electrospray ionization mode with selected reaction monitoring scan. SRM ion transitions of m/z 289 → m/z 97, m/z 289 → m/z 109, m/z 289 → m/z 79 were used for testosterone identification while m/z 401 → m/z 253, m/z 401 → m/z 271, m/z 401 → m/z 97 were employed for testosterone enanthate. Retention time and product ion intensity ratio were used as confirmation criteria to ascertain the presence of both analytes in equine plasma. The limits of detection, quantification and confirmation were 50 pg 0.5 mL^?1, 100 pg 0.5 mL^?1 and 250 pg 0.5 mL^?1, respectively for both analytes. The method was validated for recovery efficiency, sensitivity, matrix effect, linearity, precision and accuracy. This method is routinely used in the PA program for androgenic anabolic steroids doping control in racehorses and in the on-going testosterone enanthate pharmacokinetics study. The method is defensible, fast, selective, specific and reproducibly reliable.