基于大规模定制的供应信息框架研究

研究了大规模定制环境下的结构性供应关系与过程性供应关系，进而给出了表达结构性供应关系的信息表达结构MCGBOM，以及表达过程性供应关系的信息表达结构MCGSPG，并用XML标准为这两种信息结构进行了标准化描述，以用于多代理系统中的信息交换．     

Q value related mass determinations using a Penning trap

We report here about measurements of reaction and decay Q values by precise determination of pairs of atomic masses. These were performed with the Penning trap mass spectrometer SMILETRAP. Measurements with Penning traps give reliable and accurate masses, in particular Q values, due to the fact that certain systematic errors to a great deal cancel in the mass difference between the two atoms defining the Q value. Some Q values that are of fundamental interest will be discussed here, for example, a new Q value for the ⁶Li (n,γ) ⁷Li reaction, for the β-decay of tritium, related to properties of the electron neutrino mass, and for the neutrino-less double β-decay of ⁷⁶Ge, related to the question of whether the neutrino is a Majorana particle or not. In case of the latter two we report the most accurate Q values, namely 18,589.8(12) eV for the tritium decay and 2,038.997(46) keV for the neutrino-less double β-decay of ⁷⁶Ge.     

Mechanism of the thermal decomposition of nitrates from graphite furnace mass spectrometry studies

A basically new mechanism of the thermal decomposition of solids is proposed to explain the mass spectral observations of gaseous molecules of CoO, CuO, Cu₂O, NiO, PbO and Mg(OH)₂ during the low-temperature decomposition of the anhydrous and hydrated nitrates of these metals. The mechanism consists of two stages: congruent gasification of all reaction products irrespective of their saturated vapor pressure and subsequent condensation of the low-volatility species (oxides and hydroxides). The partial pressures of these species at the appearance temperatures calculated from this theory for the first stage of the process (1–50 mPa) are in agreement with the detection limits of the quadrupole mass spectrometers used in these experiments. The proposed mechanism is supported by other available data obtained by thermal analysis.     

Chemical imaging in biology and medicine using ion microscopy

The ability to quantitatively map the distribution of elements on the micrometer scale and smaller with high sensitivity and isotopic discrimination is unique to ion microscopy. The information contained in ion images can be crucial to the study of the solid state, where chemical heterogeneity is often directly related to observed behavior. The tools of digital image processing allow the extraction of quantitative information from the image data. These techniques coupled with improved instrumentation for the detection of ion images drastically increase the problem solving capabilities of the ion microscope. The use of such methods and instrumentation in the ion microscopic analyses of cell cultures and tissues of biological and biomedical relevance will be discussed.     

Radio-Frequency Hexamethyldisiloxane Plasma Deposition: A Comparison of Plasma- and Deposit-Chemistry

This study reports on the effect of input power to hexamethyldisiloxane (HMDSO) plasmas. The power dependence of the plasma-phase species and of the surface chemistry (of the deposits) has been investigated. Neutral and positive molecular species were detected within the plasma using mass spectrometry (MS). Secondary ion mass spectrometry (SIMS) was used to probe the molecular structure of the deposits. The elemental composition of the surface was determined by XPS and the deposition rate was monitored using a vibrating quartz crystal microbalance. Neutral and cationic molecules of mass greater than HMDSO were detected in the plasma. Their formation through ion-molecule reactions is proposed. Changes in the relative concentration of plasma-phase species follow those seen in molecular species detected at the deposit surface. Thus, we believe that the molecular structure of the deposits can be related to the species present in the plasma. While traditionally the dominant mechanism in deposit formation is assumed to be free radical combinations, we propose other possibilities involving cations with the aim of putting forward a new perspective on plasma polymerization mechanisms and thereby stimulating discussion.     

超微粒子－有机聚合物薄膜的研究

我们用离子团束－飞行时间质谱（ＩＣＢ－ＴｏＦＭＳ）系统制备了金（Ａｕ）超微粒子－聚乙烯（ＰＥ）薄膜和Ｃ＿（６０）－聚乙烯薄膜。用透射电子显微镜（ＴＥＭ）分析了所制备的样品。它们的结构是Ａｕ超徽粒子镶嵌在多晶的ＰＥ薄膜中，其中Ａｕ原子团呈球形，直径分布在２．０－５．０ｎｍ窄范围内，当沉积基底温度为９０℃时，Ａｕ原子团相互靠近，几乎连接起来，但仍保持原来大小。基底温度为１４０℃蒸积的Ｃ＿（６０）－ｐＥ薄膜具有晶态结构，其晶格常数为１．４５４ｎｍ。     

Pyrolysis chemical ionization mass spectrometry of cellulose ethers

Pyrolysis ammonia chemical ionization (PyCI) mass spectrometry was performed on hy-droxyethyl-, hydroxypropyl-,methyl-, hydroxypropylmethyl-, and ethylhydroxyethyl cel-luloses. The mass peaks in the PyCI mass spectra of these cellulose ethers could be assigned to the ions of pyrolytic dissociation products which form via the [2 + 2 + 2] cycloreversion and the E_i elimination pyrolysis pathway. Structural information about the residual amount of nonderivatized cellulose, the relative chain length distributions of the substituents in hydroxyalkyl celluloses, and the end-capping of hydroxyalkyl substituents by alkyl groups in the mixed cellulose ethers is obtained. Interference of secondary pyrolysis products in the PyCI mass spectra is found to be of minor importance, especially in the lower mass regions. © 1995 John Wiley & Sons, Inc.     

Chemical component exchange and transport phenomena accompanying phase transformations in minerals and materials

Chemical component exchange and transport phenomena accompanying the multistage phase transformations of several silicate and aluminosilicate-phosphate glasses and borates as model systems are considered. It is demonstrated that the component transport limitations modify the role of chemical affinity influence and determine the sequence of new compound formation.The work was supported by grant P040703406 from the National Committee of Scientific Research of Poland.     

Depth profiling of latex blends of fluorinated and fluorine‐free acrylates with laser‐induced secondary mass spectrometry

We explored phase separation and self‐assembly of perfluoroalkyl segments at the surface of polymer films obtained from latices of semifluorinated acrylate copolymers and the corresponding latex blends of nonfluorinated and semifluorinated polyacrylates. With laser‐induced secondary mass spectrometry the fluorine distribution was measured after annealing above the minimum film‐forming temperature of the polymers up to a depth of several micrometers. Depth profiles of a semifluorinated acrylate homopolymer and latex blends thereof with fluorine‐free alkylacrylates with 25, 50, and 75 mol % semifluorinated acrylate as well as a copolymer comprised of alkyl acrylate and semifluorinated acrylate (50/50 mol %) were investigated. In the case of latex blends containing both semifluorinated polyacrylates and fluorine‐free or low‐fluorine polymers, self‐assembly accounted for enrichment of the perfluoroalkyl segments at the surface. Coatings exhibiting low surface energy and having a substantially reduced total fluorine content were obtained. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 360–367, 2003     

Cooling,identification and spectroscopy of super-heavy element ions

We briefly discuss some possibilities for cooling, identification and spectroscopy of super-heavy element (SHE) ions based on recent results obtained from studies of atomic and molecular ions in linear rf traps. Since these investigations only relied on the charge and the mass of the ion of interest, we believe it should be straight forward to adopt most of the techniques for SHE ion research.