应用于同步加速器时序控制的片上可编程系统的设计

同步加速器对控制信号的时间约束要求非常严格,时序控制是加速器控制系统中十分重要的环节。在兰州重离子加速器冷却储存环(HIRFL-CSR)控制系统中,时序控制主要采用FPGA+ARM+linux+DSP的体系结构。本文介绍基于FPGA和uClinux操作系统的片上可编程系统(SOPC)的设计,可将目前ARM+LINUX的工作完全集成在FPGA内实现,省去专用ARM芯片。其最高工作频率可达185 MHz,硬件资源消耗不到4%。片上可编程系统的硬件处理器系统和操作系统都可根据具体需求重新裁剪和配置。SOPC技术在加速器物理以及其他领域有着非常广泛的应用前景。

~229Ra衰变性质的实验研究及重丰中子新核素~186Hf的搜索

用14MeV中子轰击Th靶，通过232Th（n，α）反应产生了229Ra，由放射化学分离技术从被照靶物质中分离出229Ra的活性，利用γ（X）谱学方法，首次观测到了属于229Ra的能量为14.5、15.6、18.8、21.8、22.5、44.0、47.5、55.0、63.0、69.6、93.6、94.1、98.5、102.2、104.5、106.1、161.1、171.5KeV的18条新衰变γ射线，并建议了229Ra的部分衰变纲图。 在重丰中子186Hf的搜索实验中，利用50MeV/u的18O轰击天然W靶，通过多核子转移186W（-2p+2n）反应生成186Hf，经化学分离，用高纯锗探测器和X-γ符合方法观测到其子体186Ta的能量分别为615.3、737.5、739.2-KeV的3条γ线，根据这3条γ线的生长-衰变曲线确定186Hf的半衰期为分钟量级。

Enhancement on the hydrothermal stability of ZSM-5 zeolites by the cooperation effect of exchanged lanthanum and phosphoric species

It was explored by density functional calculations that exchanged La or P species exert great influence on the local Al sites as well as on the adjacent exchanged species. In partially exchanged La- or P/H-ZSM-5 zeolite, some of the Al sites will fall off from the zeolite framework even more easily than in H-form ZSM-5, consistent with our XRF experiments. However, when exchanged by both La and P species, Al at either of the two exchanged sites shows better stability compared to H-from. zeolite. La and P species will interact strongly with each other, as evidenced by the charge donation process and the shortening of P-O-1 bond length. It was just the cooperation of La and P species that enabled RSCC catalysts worked normally under severe conditions. (C) 2004 Elsevier B.V. All rights reserved.

长期施肥对土壤活性有机碳指标的影响

以棕壤长期肥料定位试验地土壤为试材,研究和对比了不同施肥处理耕层土壤各项活性有机碳指标对长期施肥的响应。研究结果表明,长期施用化肥、有机肥以及有机肥配施化肥均显著改变了土壤总有机碳(TOC)含量。与此同时,土壤的轻组有机碳(LFOC)、易氧化有机碳(ROC)和微生物量碳(MBC)含量亦对长期施肥产生与TOC基本一致的响应。相关分析结果表明,土壤的LFOC、ROC和MBC可以作为长期施肥对土壤TOC影响的评价指标,且三者的指示灵敏度依次为MBC>LFOC>ROC。

黄土塬区旱作农田高生产力的水分环境效应与产量波动性

以长武生态站水肥产量效应的长期定位试验资料为基础，结合模型预测的分析方法，揭示出黄土高原旱作塬区高产农田的水分环境效应在于过度消耗土壤水库，降低土壤含水量，使作物生长转而过度依靠年度降水，出现年际产量的高波动性。指出旱作高产高波动性具有可持续性，它是当前旱作农业的基本特点。

Europium complexes immobilization on titania via chemical modification of titanium alkoxide

We report a facile strategy to tether lanthanide complexes to organic-inorganic hybrid titania materials via sol-gel processing by employing chemically modified titanium alkoxide as the precursor where the organic ligand sensitizing the luminescence of lanthanide ions is bonded to titanium.

Synthesis, photophysical and electrophosphorescent properties of mononuclear Pt(II) complexes with arylamine functionalized cyclometalating ligands

Four cyclometalated Pt(II) complexes, i.e., [(L-2)PtCl] (1b), [(L-3)PtCl] (1c), [(L-2)PtC CC6H5] (2b) and [(L-3)PtC CC6H5] (2c) (HL2 = 4-[p-(N-butyl-N-phenyl)anilino]-6-phenyl-2,2'-bipyridine and HL3 = 4-[p(-N,N'-dibutyl-N'-phenyl)phenylene-diamino]-phenyl-6-phenyl-2,2'-bipyridine), have been synthesized and verified by H-1 NMR, C-13 NMR and X-ray crystallography. Unlike previously reported complexes [(L-1)PtCl] (1a) and [(L-1)PtC CC6H5] (2a) (HL1 = 4,6-diphenyl-2,2'-bipyridine), intense and continuous absorption bands in the region of 300-500 nm with strong metal-to-ligand charge transfer ((MLCT)-M-1) (d pi(Pt) -> pi*(L)) transitions (epsilon similar to 2 x 10(4) dm(3) mol (1) cm (1)) at 449-467 nm were observed in the UV-Vis absorption spectra of complexes 1b, 1c, 2b and 2c.

PP-g-AA接枝共聚物的制备及表征

以部分预辐照聚丙烯(rPP)作为聚丙烯反应挤出接枝丙烯酸(AA)的引发剂,制备了PP-g-AA接枝共聚物。考察了预辐照剂量、预辐照聚丙烯用量以及单体浓度等因素对接枝反应的影响。采用红外光谱、差热扫描量热仪和偏光显微镜等测试技术对接枝产物的形态、结构及性能进行了研究。结果表明,这种新的PP-g-AA共聚物制备方法能有效抑制聚丙烯的降解并获得较高力学性能的接枝产物。研究发现,当rPP的预辐照剂量为4 kGy,反应原料的组成为m(PP)∶m(rPP)∶m(AA)=90∶10∶0.8时,得到的产物有较高的接枝率(0.19%),并且具有相对最佳的力学性能;这种接枝产物与铝板有很强的粘接效果,其剥离强度达4.88 kN/m。

Preparation, structure and oxide ion conductivity in Ce6-xYxMoO15-delta (x=0.1-1.4) solid solutions

The Ce6-xYxMoO15-delta solid solution with fluorite-related structure have been characterized by differential thermal analysis/thermogravimetry (DTA/TG), X-ray diffraction (XRD), IR, Raman, scanning electric microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) methods. The electric conductivity of samples is investigated by Ac impedance spectroscopy. An essentially pure oxide-ion conductivity of the oxygen-deficiency was observed in pure argon, oxygen and air. The highest oxygen-ion conductivity was found in Ce5.5Y0.5MoO15-delta ranging from 5.9 X 10(-5)(S cm(-1)) at 300 degrees C to 1.3 X 10(-2)(S cm(-1)) at 650 degrees C, respectively. The oxide-ion conductivities remained stable over 80 h-long test at 800 degrees C. These properties suggested that significant oxide-ionic conductivity exists in these materials at moderately elevated temperatures.

A highly reduced polyoxoanion with phosphorus-centered alternate layers of Mo/V oxides, [(PMo2Mo6V4O40)-Mo-V-V-VI-O-IV((VO)-O-IV)(2)](9-)

An unusual polyoxometalate [H2N(C2H4)(2)NH2](4)(H3O)[(PMO2Mo6V4O40)-Mo-V-V-VI-O-IV((VO)-O-IV)(2)].H2O is hydrothermally synthesized and characterized by IR, UV-VIS, elemental analyses, X-ray photoelectron spectrum, ESR, TG and Single crystal X-ray diffraction. The title compound crystallizes in the orthorhombic space group Pbca with a = 15-227(5), b = 19.491(4), c = 18.737(3) Angstrom, V = 5123(2) Angstrom(3), Z = 4, and R-1 (wR(2)) = 0.0726(0.1416). The compound contains an unusual highly reduced pseudo-Keggin type polyoxoanion and exhibits an interesting phosphorus-centered alternate arrangement of layers of molybdenum and vanadium oxides.

Synthesis, characterization and crystal structures of dibenzo-18-crown-6 sodium isopolytungstates

Two novel dibenzo-18-crown-6 sodium isopolytungstates, [(DB18C6)(CH3OH)Na](2)W(6)O(19)(.)DB18C6(.)H(2)O 1 and [(DB18C6)(DMF)(2)Na](4)W(10)O(32)(.)2DMF(.)2H(2)O 2, have been synthesized in mixed methanol and acetonitrile solvents and characterized by elemental analysis, TGA, IR and single crystal X-ray diffraction. The compound 1 crystallizes in the monoclinic space group C2/c with a = 23.182(8), b = 19.527(2), c = 18.737(3) Angstrom, beta = 115.15(2)degrees, V = 7678(3) Angstrom(3), Z = 4, and R1(wR2) = 0.0611(0.1504). The compound 2 crystallizes in the monoclinic space group P21/n with a = 16.516(2), b = 22.325(6), c = 20.425(7) Angstrom, beta = 91.78(2)degrees, V = 7528(3) Angstrom(3), Z = 2, and R1(wR2) = 0.0397(0.0773). The compound 1 exhibits a novel organic-inorganic sandwich-type structure, in which the crown ether-sodium complexes are coordinated to the terminal oxygen atoms of W6O192-. In compound 2, all Na+ ions are thoroughly enveloped into the organic moieties of crown ether and DMF molecules and are connected with the 'naked' polyanions W10O324- via the electrostatic attraction.

Synthesis and crystal structure of aluminium complex with 3-hydroxyflavone

[Al(C15H9O3)(3)](2) . 2CHCl(3) . 8H(2)O was synthesized, and its crystal structure was determined. It belongs to trigonal system, R3, a=b=1. 655 8(3) nm, c=3. 646 5(20) nm, alpha = beta = 90 degrees, gamma = 120 degrees, V = 8. 656 08(0. 005 86) nm(3). D-c = 1.45 g/cm(3), mu(Mo K alpha) = 3. 20 cm(-1), F (000) = 3 924. The crystal structure was solved by Patterson and Fourier techniques, and refined by a block-diagonal least-squares method. A total of 3 737 independent intensity data were collected, of which 1 033 with I greater than or equal to 3 sigma(I-0) were observed, R = 0. 091 8, Rw=0. 091 8. Al3+ ion was 6-coordinated, bound to six oxygen atoms from three 3-hydroxyflavones to form a distortional coordination octahedron.

利用毛细管效应的反射式显微红外光谱电化学池的设计与表征

报道一种新型的适用于水和非水溶剂的反射式现场显微红外光谱电化学池。该池利用毛细管效应来克服显微池中溶剂挥发和除氧的困难，保证电解薄层能长时间保持浸润和良好的工作状态。安装了 ５０ μｍ直径的铂微盘工作电极，分别在水溶液和二氯甲烷溶液中，用Ｆｅ（ＣＮ）６４－／３－和二茂铁体系进行了表征。