Molybdenum L-shell X-ray production by 350-600 keV Xeq+ (q=25-30) ions

Molybdenum L-shell X-rays were produced by Xeq+ (q = 25-30) bombardment at low energies from 2.65 to 4.55 keV/amu (350-600 keV). We observed a kinetic energy threshold of Mo L-shell ionization down to 2.65-3.03 keV/amu (350-400 keV). The charge state effect of the incident ions was not observed which shows that the ions were neutralized, reaching an equilibrium charge state and losing their initial charge state memory before production of L-shell vacancies resulted in X-ray production. The experimental ionization cross sections were compared with those from Binary Encounter Approximation theory. Taking into account projectile deflection in the target nuclear Coulomb field, the ionization cross section of Mo L-shell near the kinetic energy threshold was well described. (C) 2010 Published by Elsevier B.V.

《景观生态学原理与方法》简介

由国际著名景观生态学家、国际生态学会秘书长、意大利Ｌｕｎｉｇｉａｎａ自然博物馆主任法瑞纳（ＡｌｍｏＦａｒｉｎａ）博士撰写的又一部景观生态学力作《景观生态学原理与方法》（Ｐｒｉｎｃｉｐｌｅａｎｄｍｅｔｈｏｄｓｉｎｌａｎｄｓｃａｐｅｅｃｏｌｏｇｙ）已于１...

Geometries of the Halocarbene anions HCF- and CF2-: ab initio calculation and Franck-Condon analysis

A theoretical method to calculate multidimensional Franck-Condon factors including Duschinsky effects is described and used to simulate the photoelectron spectra of HCF- and CF2- radicals. Geometry optimization and harmonic vibrational frequency calculations have been performed on the (X) over tilde (1)A' state of HCF and (X) over tilde (2)A" state of HCF-, and (X) over tilde (1)A(1) state of CF2 and (X) over tilde B-2(1) state of CF2-. Franck-Condon analyses and spectral simulation were carried out on the first photoelectron band of HCF- and CF2- respectively. The theoretical spectra obtained by employing B3LYP/6-311 + G(2d,p) values are in excellent agreement with the observed ones. In addition, the equilibrium geometry parameters, R(CF) = 0.1475 +/- 0.0005 nm, of the (X) over tilde (2)A" state of HCF-, and r(FC) = 0.1425 +/- 0.0005 nm and angle(FCF) = 100.5 +/- 0.5degrees, of the (X) over tilde B-2(i) state of CF2-, are derived by employing an iterative Franck-Condon analysis procedure in the spectral simulation. (C) 2003 Elsevier B.V. All rights reserved.

长白山地区蒙古栎光合特性

基于单叶尺度上的光强-光合响应以及CO2-光合响应测定,对长白山地区蒙古栎成树和幼树的光合特性分别进行了研究.结果表明,蒙古栎成树的光补偿点Lcp为21μmol/(m2·s),光饱和点Lsp为1564μmol/(m2·s),表观量子效率α为0·045;幼树的Lcp、Lsp、α以及CO2补偿点、饱和点分别为29μmol/(m2·s)、1581μmol/(m2·s)、0·049、73μmol/mol、625μmol/mol.幼树和成树具有相似的光响应特征,但前者的光合同化能力要高于后者.蒙古栎具有典型的喜光性,但对高光的利用效率要低于弱光.

脲酶抑制剂/硝化抑制剂对植稻土壤中尿素N行为的影响

采用自制根盒试验 ,主要研究了脲酶抑制剂氢醌 (HQ)、硝化抑制剂双氰胺 (DCD)及二者组合对离水稻根际不同距离处 NH+ 4-N和 NO- 3 -N分布的影响。结果表明 ,DCD及其与 HQ组合均能显著促进稻株地上部分生长 ,始终显著降低水稻根际与近根际土中 NH+ 4-N含量直至施肥后 60 d。施肥后 2 0 d时 ,DCD及其与 HQ组合可使非根际土中 NH+ 4-N含量显著增加。随后 ,却出现相反现象。施肥后 2 0 d时 ,距根际不同距离的土壤中 ,配施 DCD或 DCD+HQ处理均能显著降低NO- 3 -N含量。随后 ,近根际和非根际仍保持上述现象直至施肥后 40 d;同未施 DCD处理相比 ,根际土壤却较早出现NO- 3 -N含量高峰 ,正好与水稻 N营养需求时期相一致。因此 ,DCD及其与 HQ组合可减少水稻根际环境下尿素 N损失潜势。通过不种稻土壤和距根际 3 cm处的土壤中尿素无机氮形态分布的差异 ,充分显示了研究水稻根际土壤氮素转化及相关抑制剂对其影响时 ,以取离根际 3 cm外的土壤作为非根际明显优于不种稻土壤。

Ruby:一个基于移动设备的个人信息管理系统

为满足移动环境对非结构化个人信息管理的自然性和高效性的需求,提出一个基于移动设备的个人信息管理系统Ruby.首先分析了移动环境对个人信息管理的需求,描述了系统框架,接着介绍了系统界面和交互过程,并阐述了支持该系统的2个主要技术:非结构化笔记编辑技术和基于笔迹标签的检索技术.对2个技术和整个系统的评估结果表明,该系统能够满足移动环境对自然交互、非结构化信息采集加工及个人信息自然检索的需求.

Guest inducing p-sulfonatocalix[4] arene into three-dimensional capsule architecture and a mixed A-B double layer framework

The reactions of sodium p-sulfonatocalix[4]arene (Na5L) and terbium/europium(III) chloride in the presence of pyrazine-N,N'-dioxide (PNNO) in aqueous solutions gave the crystalline complexes 1 and 2. Both structures contain molecular capsules of p-sulfonatocalix[4] arene with PNNO as guest molecules in the cavity of the calix[4]arenes. The molecular capsules are connected through sodium and terbium (or europium) centers forming a three-dimensional framework.

Pechini sol-gel deposition and luminescent properties of SrLa1-xRExGa3O7 (RE = Eu, Tb) phosphor films

SrLa1-xRExGa3O7 (RE = EU3+, Tb3+) phosphor films were deposited on quartz glass substrates by a simple Pechim sol-gel method. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), atomic force microscopy, field-emission scanning electron microscopy, photoluminescence spectra, and lifetimes were used to characterize the resulting films. The results of XRD indicated that the films began to crystallize at 700 degrees C and crystallized fully at 900 degrees C. The results of FNR spectra were in agreement with those of XRD. Uniform and crack-free films annealed at 900 degrees C were obtained with average grain size of 80 nm, root mean square roughness of 46 nm and thickness of 130 nm The RE ions showed their characteristic emission in crystalline SrLa1-xRExGa3O7 films, i.e., Eu3+ D-0-F-7(J) (J = 0, 1, 2, 3, 4), Tb3+5D4 -(7) F-J (J = 6, 5, 4, 3) emissions, respectively. The optimum concentrations (x) of Eu3+ and Tb3+ were determined to be 50, and 80 mol% in SrLa(1-x)RE(x)GGa(3)O(7) films, respectively.

Isothermal crystallization of poly(3-hydroxybutyrate-co-3-hydroxyvalerate)

Isothermal crystallization behavior of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) was investigated by means of differential scanning calorimetry and polarized optical microscopy (POM). The Avrami analysis can be used successfully to describe the isothermal crystallization kinetics of PHBV, which indicates that the Avrami exponent n = 3 is good for all the temperatures investigated. The spherulitic growth rate, G, was determined by POM. The result shows that the G has a maximum value at about 353 K. Using the equilibrium melting temperature (448 K) determined by the Flory equation for melting point depression together with U-* = 1500 cal mol(-1), T-infinity = 30 K and T-g = 278 K, the nucleation parameter K-g was determined, which was found to be 3.14+/-0.07 x 10(5) (K-2), lower than that for pure PHB. The surface-free energy sigma = 2.55 x 10(-2) J m(-2) and sigma(e) = 2.70+/-0.06 x 10-2 J m(-2) were estimated and the work of chain-folding (q = 12.5+/-0.2 kJ mol(-1)) was derived from sigma(e), and found to be lower than that for PHB. This implies that the chains of PHBV are more flexible than that of PHB.

Correlation analysis of the structures and stability constants of gadolinium(III) complexes

To simplify the abstraction of descriptors, for the correlation analysis of the stability constants of gadolinium(III) complexes and their ligand structures, aiming at gadolinium(III) complexes, we only considered the ligands and ignored the common parts of the structures, i.e., the metal ions. Quantum-chemical descriptors and topological indices were calculated to describe the structures of the ligands. Multiple regression analysis and neural networks were applied to construct the models between the ligands and the stability constants of gadolinium(III) complexes and satisfactory results were obtained.

Effect of rare earth element on the metabolism in rats by high resolution proton nuclear magnetic resonance spectroscopy

The high-field nuclear magnetic resonance (NMR) spectra can be used for the rapid multicomponent analysis in small amounts of biological fluids. In this paper, the effect of La (NO3)(3) on the rats' metabolism in urine was investigated by H-1 NMR analysis. The experimental groups of wistar rats were injected intraperitoneally with La(NO3)(3) at doses of 0.2, 2.0, 10 and 20mg/kg body weight. The remarkable variation of low molecular weight metabolites in urine has been identified by H-1 NMR spectra, in which dimethylamine, N, N-dimethylglycine, urea, alpha -ketoglutarate, trimethylamine N-oxide, succinate, citrate and amino acids have been suggested as NMR markers for renal damage and ethanol, lactate, taurine as the markers for liver damage. This work may assess its possible use in the early detection of biochemical changes associated with Rare Earth induced kidney and liver dysfunction.

稀土对大鼠代谢产物影响的核磁共振研究

以高场核磁共振技术为研究手段，通过分析腹腔注射０．２、２、１０、２０ｍｇ／ｋｇ体重剂量 的Ｌａ（ＮＯ３）。后大鼠尿液中代谢物浓度、物种的变化，研究了稀土化合物在动物体内的作用 情况，结果表明稀土的引入使动物肾脏和肝脏都受到一定程度的损伤。并在代谢物中挑选出 了合适的ＮＭＲ　ｍａｒｋｅｒｓ，其变化可以反映稀土离子作用后大鼠的异常代谢。

Electrochemical growth and characterization of polyoxometalate-containing monolayers and multilayers on alkanethiol monolayers self-assembled on gold electrodes

A general strategy has been developed for fabrication of ultrathin monolayer and multilayer composite films composed of nearly all kinds of polyoxometalates (POMs), including isopolyanions (IPAs), and heteropolyanions (HPAs). It involves stepwise adsorption between the anionic POMs and a cationic polymer on alkanethiol (cysteamine and 3-mercaptopropionic acid) self-assembled monolayers (SAMs) based on electrostatic interaction. Here a Keggin-type HPA SiMo11VO405- was chosen as a main representative to elucidate, in detail, the fabrication and characterization of the as-prepared composite films. A novel electrochemical growth method we developed for film formation involves cyclic potential sweeps over a suitable potential range in modifier solutions. It was comparatively studied with a commonly used method of immersion growth, i.e., alternately dipping a substrate into modifier solutions. Growth processes and structural characteristics of the composite films are characterized in detail by cyclic voltammetry, UV-vis spectroscopy (UV-vis), X-ray photoelectron spectroscopy (XPS), micro-Fourier transform infrared reflection-absorption spectroscopy (FTIR-RA), and electrochemical quartz crystal microbalance (EQCM). The electrochemical growth is proven to be more advantageous than the immersion growth. The composite films exhibit well-defined surface waves characteristic of the HPAs' redox reactions. In addition, the composite films by the electrochemical growth show a uniform structure and an excellent stability. Ion motions accompanying the redox processes of SiMo11VO405- in multilayer films are examined by in situ time-resolved EQCM and some results are first reported. The strategy used here has been successfully popularized to IPAs as well as other HPAs no matter what structure and composition they have.