玻色─爱因斯坦关联半径和源半径对实验窗口的依赖及它们的差异

研究了１６０ＡＧｅＶＰｂ＋Ｐｂ反应中π源的玻色─爱因斯坦关联半径和源半径（均方根半径）的关系，以及它们对实验窗口的依赖。模型冗源由ＵＲＡＳｉＭＡ生成器产生。研究表明关联半径和源半径不仅数值不等，而且变化行为也不同。     

Cross section of the impact single ionization of B2＋ by H＋

The ionization process of B2+ by H+ impact is studied using the continuum-distorted-wave eikonal-initial-state (CDW-EIS) method and the modified free electron peak approximation (M-FEPA), respectively. Total, single-, and double- differential cross sections from 1s and 2s orbitals are presented for the energy range from 10 keV/u to 10 MeV/u. Comparison between the results from the two methods demonstrates that the total and single-differential cross sections for the high-energy incident projectile case can be well evaluated using the simple M-FEPA model. Moreover, the M-FEPA model reproduces the essential features of the binary-encounter (BE) bump in the double-differential cross sections. Thus, the BE ionization mechanism is discussed in detail by adopting the M-FEPA model. In particular, the double- and single-differential cross sections from the 2s orbital show a high-energy hip, which is different from those from the 1s orbital. Based on Ref. [1], the Compton profiles of B2+ for 1s and 2s orbitals are given, and the hips in DDCS and SDCS from the 2s orbital are explained.     

Effect of Polyvinylpyrrolidone on the States of Water in Water-in-Oil Microemulsions with Betaine Surfactant

A water-in-oil (w/o) microemulsion was prepared with the zwitterionic surfactant dodecyl betaine (C₁₂BE), n-pentanol (C₅OH), n-heptane (C₇H₁₆) and water. Effects of polyvinylpyrrolidone (PVP) with different molecular weight on the state of water in w/o microemulsions at a given water/C₁₂BE molar ratio were investigated by FT-IR and differential scanning calorimetry (DSC). The experimental results showed that addition of PVP resulted in an increase of the content of the bound water in water pool of a w/o microemulsion, but a decrease of the amount of the bulky water. The higher the molecular weight of PVP, the more bound water; and the less bulk water. The change of the trapped water was not obvious due to the interference of C₅OH.     

十二烷基甜菜碱/十二烷基硫酸钠复配体系的表面活性

研究了两性表面活性剂十二烷基甜菜碱（C12BE）和阴离子型表面活性剂十二烷基硫酸钠（SDS）复配体系的形成胶束能力,降低表面张力效率,降低表面张力能力三种增效作用.发现C12BE和SDS摩尔比为6 :4时增效作用最显著.并考察了盐、醇对复配体系表面活性的影响,结果表明,加盐能导致表面活性的提高,加醇的机理比较复杂,乙醇对复配体系表面活性影响不大,而正丁醇影响则比较显著.     

聚乙烯吡咯烷酮存在时反相微乳液中水的状态

运用傅立叶变换红外光谱（FTIR）研究不同分子量的聚乙烯吡咯烷酮（PVP）存在时,十二烷基甜菜碱(C12BE)/正庚烷 /正戊醇 /水（Ⅰ）及二（2 乙基）己基磺化琥珀酸钠（AOT）/正庚烷 /水（Ⅱ） 反相微乳液中水的存在状态.采用计算机分峰技术将微乳液中水分子的O－H伸缩振动进行曲线拟合, （Ⅰ）得到三个子峰,分别位于(3560±20)cm－1,(3430±10)cm－1,(3280±10)cm－1附近; （Ⅱ）得到四个子峰,分别位于3618 cm－1, 3550 cm－1, 3446 cm－1和3292 cm－1处.尽管PVP均增溶于W/O型微乳液中表面活性剂分子的极性基团附近,却没有引起长链间自由水的变化.但由于两体系的差异,PVP的存在,导致微乳液（Ⅰ）的本体水减少,结合水增多,却使体系（Ⅱ）的结合水减少,本体水增多.由于W/O型微乳液中水与生物膜中水相似,这些研究有助于理解生物膜界面上的生物化学和生物物理现象.     

Highly sensitive capillary electrophoresis-mass spectrometry for rapid screening and accurate quantitation of drugs of abuse in urine

The combination of capillary electrophoresis (CE) and mass spectrometry (MS) is particularly well adapted to bioanalysis due to its high separation efficiency, selectivity, and sensitivity; its short analytical time; and its low solvent and sample consumption. For clinical and forensic toxicology, a two-step analysis is usually performed: first, a screening step for compound identification, and second, confirmation and/or accurate quantitation in cases of presumed positive results. In this study, a fast and sensitive CE-MS workflow was developed for the screening and quantitation of drugs of abuse in urine samples. A CE with a time-of-flight MS (CE-TOF/MS) screening method was developed using a simple urine dilution and on-line sample preconcentration with pH-mediated stacking. The sample stacking allowed for a high loading capacity (20.5% of the capillary length), leading to limits of detection as low as 2 ng mL⁻¹ for drugs of abuse. Compound quantitation of positive samples was performed by CE-MS/MS with a triple quadrupole MS equipped with an adapted triple-tube sprayer and an electrospray ionization (ESI) source. The CE-ESI-MS/MS method was validated for two model compounds, cocaine (COC) and methadone (MTD), according to the Guidance of the Food and Drug Administration. The quantitative performance was evaluated for selectivity, response function, the lower limit of quantitation, trueness, precision, and accuracy. COC and MTD detection in urine samples was determined to be accurate over the range of 10–1000 ng mL⁻¹ and 21–1000 ng mL⁻¹, respectively.     

C14BE与NaCMC之间的相互作用(Ⅰ)──NaCMC对C14BE表面活性的影响

以表面张力法研究了NaCMC与C₁₄BE之间的相互作用。结果表明:在纯水介质中,NaCMC对C₁₄BE的表面活性影响较小,但NaCl的存在对C₁₄BE与NaCMC间的缔合有促进作用,混合体系的σ～C曲线出现两个转折点。二者开始缔合的浓度小于cmc,完成缔合的浓度大于cmc.pH=2时,形成C₁₄BE/H-CMC复合物,使C₁₄BE的表面活性降低,σ～C曲线亦出现两个转折点。     

变水深坝—库系统耦振分析的边界元—有限元混合法

常用的混合元法解变水深坝－库系统的耦振，需要对变水深部分的流场进行域离散，计算工作量大，该文利用Ｆｒｉｅｄｍａｎ的算子函数理论，构造了势流问题在无限长带形域中的Ｇｒｅｅｎ函数，从而使流场的边界元剖分只限于变水深区域的边界，关于坝体仍采用有限元离散，最后借助所导出的有限元－边界元格式对坝－库系统的实例作了数值计算，结果证明了它的有效性。     

Some applications of boundary element methods, boundary element-finite element coupling techniques in elasto-plastic stress analysis

In this paper some research works of author's group on boundary element method for linear elastic and elasto-plastic problems are briefly summarized. The BE subrogions method and BE-FE coupling techniques are introduced, and some idea of the error estimation of BE solutions is presented.This work is supported by the National Natural Science Foundation of China.