同位旋非对称核物质性质与扩展的BHF方法(Ⅰ)同位旋相关的扩展的BHF方法

通过引进基态关联和同位旋自由度的区分,推广了Brueckner Hartree Fock理论方法,并应用于同位旋非对称核物质,系统地研究了在整个同位旋自由度范围内核物质的状态方程和单粒子特性及其同位旋效应.还研究了微观三体核力对同位旋非对称核物质性质及其同位旋效应的影响,定量讨论了三体力效应与相对论性平均场理论及Dirac Brueckner方法的联系.主要给出了同位旋相关的Brueckner Hartree Fock方法的基本理论和计算公式.     

Two-loop Majorana neutrino mass and magnetic moment in a gauge model

Two-loop contributions to Majorana mass and transition magnetic moment in a gauge model not in conflict with decaying neutrino dark matter (DDM) hypothesis have been studied. Another variant of an earlier model [J Dhar and S Dev,Pramana — J. Phys. 39 541 (1992)] consistent with the DDM hypothesis is proposed and is shown to lead to large enough neutrino magnetic moment and consistent with the phenomenological constraints on neutrino mass.     

浅谈近场光学

简要地介绍了近场光学的历史及现状，讨论了近场光学显微镜的构造、工作原理、工作方式及实际应用，并支近场光学的一些理论问题作了简明扼要的介绍，指出理论和实验上需要进一步发展的地方以及可能的途径。     

核物质中的三体核力效应和相对论效应

在BHF理论框架内,利用两体现实核力和微观三体核力研究了核物质状态方程,仔细计算和分析了核介质中不同的基本微观过程导致的三体核力对核物质状态方程的贡献,与相对论DBHF方法的计算进行了比较.结果表明,DBHF方法中包含的对核物质状态方程的主要相对论修正来自于核介质中伴随着自由核子–反核子对虚激发中间过程对核子相互作用中标量σ介子交换过程介质修正效应所导致的三体核力,而来自于其他的基本微观过程的三体核力对核物质状态方程的贡献并不能完全相互抵消,它们的总贡献甚至在饱和密度附近也是不能忽略的     

聚乙烯醇缩对甲酰基苯偶氮变色酸液—固萃取分离镉,铜,镍

研究了高分子显色剂聚乙烯醇缩对甲酰基苯偶氮变色酸作萃取剂时，Ｃｄ＾２＋，Ｃｕ＾２＋，Ｎｉ＾２＋的非有机溶剂液－固萃取行为，并与相应的小分子试剂对甲酰基苯偶氮变色酸作比较。结果表明，在吐温－８０－硫酸钠－水体系中ＰＶＡ．ＦＰＮＳ作萃取剂比ＦＰＮＳ更易获得高的萃取率和好的分离效果。     

Trace sulfide determination in oxic freshwaters

A simplified method for determination of reduced sulfur species in natural waters is presented. Reduced sulfur species were separated from a natural water matrix, using purge-and-trap (PT), after reacting with acid (acid volatile sulfide—AVS) or Cr(II) in acidic medium (chromium reducible sulfur—CRS). Sulfide in the trapping medium (0.05 M NaOH), was analyzed spectrophotometrically after derivatization to form methylene blue (MB). AVS precision for Na₂S and zinc sulfide clusters in synthetic solutions was ≤8.5% RSD at concentrations ranging from 48 to 503 nM. Spike recoveries of zinc sulfide clusters were 75-98% in a variety of freshwaters using the AVS procedure. Spike recoveries of Cu sulfide colloids were 94-109% in the same freshwater samples using the CRS procedure. During the analytical procedure an interfering compound was produced due to the reaction of mixed diamine reagent with itself. Lowering the pH of the reaction mixture minimized the formation of this compound. Minimizing contamination from particulates was necessary to achieve sub-nanomolar detection limits. The detection limit for AVS in a 500 ml sample with a 10 cm spectrophotometer cell was 0.1-0.3 nM (3×S.D. blank). The CRS procedure was calibrated with a synthetic CuS colloid. Interferences to the CRS method included finely divided pyrite, polysulfide, thiosulfate, sulfite and some elemental sulfur. The Cr(II) reagent did not reduce sulfate under our experimental conditions. The degree to which zinc sulfide clusters were adsorbed on membrane filters during filtration was mitigated if the clusters were synthesized in the presence of natural organic matter. Examples of AVS and CRS concentrations determined in oxygenated waters using the PT method were comparable to those reported recently by other methods. This method offers greater simplicity than other methods for trace dissolved sulfide determination in natural waters.     

Recent developments in manufacturing emulsions and particulate products using membranes

Membrane emulsification (ME) is a relatively new technique for the highly controlled production of particulates. This review focuses on the recent developments in this area, ranging from the production of simple oil-in-water (O/W) or water-in-oil (W/O) emulsions to multiple emulsions of different types, solid-in-oil-in-water (S/O/W) dispersions, coherent solids (silica particles, solid lipid microspheres, solder metal powder) and structured solids (solid lipid microcarriers, gel microbeads, polymeric microspheres, core-shell microcapsules and hollow polymeric microparticles). Other emerging technologies that extend the capabilities into different membrane materials and operation methods (such as rotating membranes, repeated membrane extrusion of coarsely pre-emulsified feeds) are introduced. The results of experimental work carried out by cited researchers in the field together with those of the current authors are presented in a tabular form in a rigorous and systematic manner. These demonstrate a wide range of products that can be manufactured using different membrane approaches. Opportunities for creation of new and novel entities are highlighted for low throughput applications (medical diagnostics, healthcare) and for large-scale productions (consumer and personal products).     

Das erste Gadoliniumcarbidfluorid: Gd2CF2

The First Gadolinium Carbide Fluoride: Gd₂CF₂ Gd₂CF₂, the first gadolinium carbide fluoride is prepared by reaction of stoichiometric amounts of GdF₃, Gd, and C at 1250°C in sealed Ta-capsules. It is isotypic with Gd₂CBr₂ (space group P3 m1; a = 373.11(4) and c = 642.5(1) pm). The Gd atoms surround the C atoms octahedrally. Such Gd₆C octahedra are condensed via edges to form octahedral sheets, which are separated by double slabs of F^?? ions.