Properties and structure of N = Z nuclei within relativistic mean field theory

The axially deformed relativistic mean field theory with the force NLSH has been performed in the blocked BCS approximation to investigate the proper-ties and structure of N=Z nuclei from Z=20 to Z=48. Some ground state quantities such as binding energies, quadrupole deformations, one/two-nucleon separation energies, root-mean-squaxe (rms) radii of charge and neutron, and shell gaps have been calculated. The results suggest that large deformations can be found in medium-heavy nuclei with N=Z=38-42. The charge and neutron rms radii increase rapidly beyond the magic number N=Z=28 until Z=42 with increasing nucleon number, which is similar to isotope shift, yet beyond Z=42, they decrease dramatically as the structure changes greatly from Z=42 to Z=43. The evolution of shell gaps with proton number Z can be clearly observed. Besides the appearance of possible new shell closures, some conventional shell closures have been found to disappear in some region. In addition, we found that the Coulomb interaction is not strong enough to breakdown the shell structure of protons in the current region.

快重离子在SiO2基材料中引起的强电子激发效应研究

具有特殊结构的SiO2基材料与Si平面工艺具有好的兼容性，在光电技术中的发光二极管、固体显示屏等器件的研制方面有巨大的潜在应用价值。本论文以快重离子与物质相互作用的特点为依据，选择具有重要应用价值的SiO2基材料，研究快重离子辐照在SiO2基材料中引起的强电子激发效应，特别是辐照相变等现象，探索制备具有特殊功能的新型材料的方法，主要开展了如下研究： 1）在单晶Si衬底上通过高温湿法氧化一层SiO2薄膜，制备出SiO2/Si样品；在室温条件下，用能量为100 keV的碳离子注入样品，注入剂量分别为2.0×1017、5.0×1017和1.2×1018 ions/cm2，使样品SiO2薄膜中一定区域内C、Si和O原子达到适当的原子浓度配比；再用能量为308 MeV的Xe和853 MeV的Pb离子在室温下对注碳后的SiO2/Si样品进行辐照，Xe离子辐照是在兰州重离子加速器国家实验室的扇聚焦回旋加速器（HIRFL-SFC）的重离子辐照终端上完成，辐照剂量分别为1.0×1012、5.0×1012、1.0×1013、1.0×1014 Xe-ions/cm2，Pb离子辐照实验是在法国重离子激光交叉学科研究中心(CIRIL,Caen)的中能离子辐照终端（IRASME）完成的，辐照剂量分别为5.0×1011、1.0×1012、2.0×1012、5.0×1012 Pb-ions/cm2；最后用荧光光谱、红外吸收光谱、拉曼光谱和透射电子显微镜分析等技术对样品进行了表征。研究了样品发光与注碳剂量、辐照剂量和离子在薄膜中电子能损值的依赖关系，辐照引起SiO2薄膜中微结构改变与实验参数的依赖关系。发现快重离子辐照能显著改变注碳SiO2/Si样品的发光特性，如在5.0×1012 Pb-ions/cm2辐照的注碳2.0×1017 ions/cm2的样品中，探测到了很强的位于456、484和563nm的发光；在电镜照片中观察到了8H-SiC纳米晶及其他微结构的形成。基于实验结果，对薄膜发光特性与微结构改变之间的关系进行了初步探讨。 2）利用磁控溅射在单晶SiO2表面沉积Ni薄膜，制备了Ni/SiO2样品；在室温下用能量为308MeV的Xe和853MeV的Pb离子辐照Ni/SiO2样品，离子穿透Ni薄膜和Ni/SiO2界面，Xe、Pb离子辐照分别在HIRFL-SFC和法国CIRIL的IRASME辐照终端上完成，辐照剂量为1.0×1012、5.0×1012 Xe/cm2和5.0×1011Pb/cm2；用卢瑟福背散射技术和X射线衍射谱对样品进行了分析，研究了界面原子混合及相变效应与辐照剂量、电子能损值的依赖关系。发现快重离子辐照能引起Ni/SiO2样品界面处原子的混合，并导致界面形成NiSi2或Ni3Si新相，且原子扩散量随辐照剂量和电子能损值的增大而增大。 3）以热峰模型原理为基础，对实验观测到的快重离子辐照效应特别是电子能损效应的产生机理进行了探讨

不同种植制度土壤氧化还原酶活性和动力学特征

土壤质量与土壤的生物学性质密切相关,种植制度对土壤生物学特性的影响研究对土壤质量管理具有重要的意义。以黑龙江853农场不同种植制度土壤为研究对象,探讨种植制度对土壤理化性质,过氧化氢酶、脱氢酶活性和动力学特征的影响。主要研究结果:农作物轮作有利于提高土壤全碳含量,而大豆连作和玉米-大豆轮作使土壤有效氮和全氮含量提高,大豆连作土壤pH显著低于其它作物连作及轮作处理,全磷含量显著高于其它处理;2种轮作体系均提高土壤过氧化氢酶活性和催化能力,且催化能力的提高源于酶的Km降低(即酶-底物亲合力提高);玉米-小麦-大豆轮作提高土壤脱氢酶活性及催化能力,其催化能力的提高由2个动力学参数的变化共同决定,禾本科作物连作土壤动力学参数与豆科作物种植(大豆连作及与禾本科轮作)具有显著差异。本文的研究表明,合理的轮作方式是提高土壤生物学活性的有效手段。

营养元素调控下南瓜组培根化感作用的初步研究

通过调节B5培养基中的组分,研究了金钩南瓜组培根在五种营养元素(P、Mg、Fe、Cu、B)四个浓度梯度(1/2 B5、B5、3/2 B52、B5)培养下化感作用的响应模式以及对黑籽和金钩南瓜两种受体幼苗生长的影响。结果表明:不同营养元素对受体植物幼苗生长的影响不一致,与元素含量显著相关,而且依赖于受体选择。五种营养元素在亏缺(1/2 B5)和正常(B5)条件下南瓜组培根过滤液对受体植物幼苗生长均表现为抑制作用;而适量增加营养元素的条件下(3/2 B5和2 B5),一般表现为促进作用,但2 B5含量下,B元素导致金钩南瓜的自毒作用,而Fe能引发金钩南瓜组培根过滤液对黑籽南瓜的抑制作用。因此理论上初步得出P和Mg元素可以降低南瓜根系的毒害作用,而Fe、Cu和B元素对南瓜根系的化感调控作用与品种选择有关,这对调控施肥、降低设施农业中葫芦科作物的连作障碍具有一定的参考意义。

三江平原岗地白浆土水解酶活性和动力学特性对不同连作农作物的响应

作物种植会对农田生态系统产生一定的影响。大田试验条件下,在黑龙江省853农场岗地白浆土上连续6年种植玉米、大豆、小麦、水稻,研究了土壤理化性质以及土壤中与碳、氮、磷、硫元素转化相关的9种水解酶活性和动力学特性的响应;同时研究了不同作物种植对土壤脲酶、磷酸单酯酶、磷酸二酯酶、芳基硫酸酯酶及β-葡糖苷酶动力学特性的影响。结果表明,大豆连作土壤的有效氮、总碳、总氮、总磷和总硫含量都稍高;大豆处理土壤pH值略低,但其它三种作物种植下的土壤均呈微酸性,差异不显著。土壤水解酶动力学参数对种植作物的反应与表观活性的反应不一致。玉米连作土壤蛋白酶和磷酸单酯酶活性高于其它处理;小麦处理的磷酸二酯酶和芳基硫酸酯酶活性最高,水稻连作土壤蛋白酶、磷酸二酯酶和磷酸三酯酶活性最低。连年种植小麦处理的土壤脲酶、磷酸二酯酶以及芳基硫酸酯酶Vmax显著高于其它处理,小麦连作土壤β-葡萄糖苷酶、脲酶、磷酸二酯酶和芳基硫酸酯酶的Vmax/Km值显著高于其它处理,可以看出在此处理下土壤酶具有较强的催化潜势。

蓝光萘酰亚胺发光材料的合成与表征

通过在4位引入不同芳香基团,采用Suzuki和Stille偶联反应,设计与合成了一系列新型1,8-萘酰亚胺类荧光染料,并研究了它们的紫外-可见吸收、荧光发射和电化学行为等光物理性质。这些化合物在甲苯中均发射蓝色荧光,最大吸收和荧光发射峰分别在357～378和423～451nm之间,且随着芳香基团供电性增强,吸收和荧光发射波长发生红移。芳香基团的结构对化合物的发光效率影响很大,其中,取代基为甲氧基苯的化合物具有最高的荧光量子效率,可达0.98,而取代基为噻吩的化合物荧光量子效率最低,只有0.17。电化学循环伏安研究表明该类化合物具有较高的电子亲合力,不同芳香基团的引入只影响化合物的被占分子轨道(HOMO)能级,而对化合物的最低空分子轨道(LUMO)能级没有影响,即LUMO能级由1,8-萘酰亚胺单元决定。

兽疫链球菌变异株产生的透明质酸的纯化及表征

用 N-甲基 -N′-硝基 -N-亚硝基胍 ( NTG)对兽疫链球菌进行诱变 ,获得高产菌株 .经过对该菌株的发酵培养 ,将产生的多糖经 Savage法、季铵复合物沉淀法、DEAE-纤维素 ( DE5 2 )离子交换层析法及 SephadexG-75凝胶过滤法分离纯化 .纯化的多糖结构经化学组成分析、核磁共振波谱、红外光谱及圆二色谱鉴定 ,证明了诱变得到的高产菌株 ( Streptococcuszooepidemicus J1 8)再经发酵 ,得到的多糖为透明质酸 .通过刚果红实验证明了透明质酸的构象为单股螺旋结构 ,其平均分子量约为 1.16×106.

NMR and pattern recognition studies on the acute biochemical effects of Lu(NO3)(3)

Pattern recognition methods were applied to the analysis of 600 MHz H-1 NMR spectra of urine from rats dosed with compounds that induced organ-specific damage in the liver and kidney. Male Wistar rats were separated into groups (n=4) and each was treated with one of following compounds: HgCl2, CCl4, Lu(NO3)(3) and Changle (a kind of rare earth complex mixed with La, Ce, Pr and Nd). Urine samples from the rats dosed with HgCl2, CCl4 and Lu(NO3)(3) were collected over a 24 h time course and the samples from the rats administrated with Changle were gained after 3 months. These samples were measured by 600 MHz NMR spectroscopy. Each spectrum was data-processed to provide 223 intensity-related descriptors of spectra. Urine spectral data corresponding to the time intervals, 0-8 h (HgCl2 and CCl4), 4-8 (Lu(NO3)(3)) h and 90 d (Changle) were analyzed using principal component analysis (PCA). Successful classification of the toxicity and biochemical effects of Lu(NO3)(3) was achieved.

In situ synthesis and characterization of multiwalled carbon nanotube/Au nanoparticle composite materials

An effective and facile in Situ reduction approach for the fabrication of carbon nanotube-supported Au nanoparticle (CNT/Au NP) composite nanomaterials is demonstrated in this article. Linear polyethyleneimine (PEI) is ingeniously used as both a functionalizing agent for the multiwalled carbon nanotubes (MWNTs) and a reducing agent for the formation of An NPs. This method involves a simple mixing process followed by a mild heating process. This approach does not need the exhaustive surface oxidation process of CNTs. The coverage of Au NPs on CNTs is tunable by varying the experimental parameters, such as the initial molar ratio of PEI to HAuCl4, the relative concentration of PEI and HAUCl(4) to MWNTs, and the temperature and duration of the heat treatment. More importantly, even the heterogeneous CNT/Au composite nanowires are obtainable through this method. TEM, XPS, and XRD are all used to characterize the CNT/Au composite materials. In addition, the optical and electrocatalytic properties are investigated.

Electrochemiluminescence of tris(2,2 '-bipyridyl)ruthenium (II) ion-exchanged in polyelectrolyte-silica composite thin-films

The organic-inorganic hybrid, PSS-silica composite material was developed for the immobilization of tris(2,2'-bipyridyl)ruthenium(II) (Ru(bpy)(3)(2+)) on glassy carbon electrode via ion-exchange (PSS stands for poly(sodium 4-styrene-sulfonate)). The electrochemiluminescence (ECL) and electrochemistry of Ru(bpy)(3)(2-) immobilized in the composite thin films have been investigated with tripropylamine (TPA) as the coreactant. The immobilized Ru(bpy)(3)(2-) underwent a surface process. The modified electrode was used for the ECL detection of TPA and showed high sensitivity. Detection limit was 0,1 mumol L-1 for TPA (S/N = 3) with a linear range from 0.5 mumol L-1 to 5 mmol L-1 (R = 0.998), Moreover, the resulting modified electrode was stable over six months and the good stability may be due to the strong interaction between Ru(bpy)(3)(2-) and the high ion-exchange able PSS-silica composite films on GCE. Compared with other materials. the PSS-silica composite films containing incorporated Ru(bpy)(3)(2-) showed improved sensitivity and long-term stability, Thus, such composite thin film can be a promising material for the construction of ECL sensor.

Synthesis, properties and crystal structure of organic-inorganic radical salt (DBTTF)(6)HPMo12O40 center dot 2H(2)O

Organic-inorganic radical salt (DBTTF)(6)PMo12O40 . 2H(2)O was synthesized by electrocrystallization and characterized by IR spectrum, electronic spectrum and ESR technology, Its magnetic property, conductivity and crystal structure were determined. The title compound crystallized in a triclinic system with P1 space group, a = 1.378 7(7), b = 1.420 4 (2), c = 1.570 2(2) nm, alpha = 104.57(1)degrees, beta = 103.41(2)degrees, gamma = 95.80(2)degrees, V = 2.853(2) nm(3) Z = 1 and a final R = 0.072 7.

含全双硫螯合配体簇合物的研究——Ⅱ.[Mo_2Fe_2(μ_3-S)_4(S_2CNEt_2)_5]·CH_3CN的合成、结构和性质

在无氧非水介质中,以(NH_4)_2MoS_4,FeCl_3和NaS_2CNEt_2为原料合成了簇合物 [Mo_2Fe_2S_4(S_2CNEt_2)_5]·CH_3CN.X射线单晶结构测定表明,它具有[Mo_2Fe_2S_4]~(5+)类立方烷核心骨架。每个金属原子有一螯合基团S_2CNEt_2配位。第五个S_2CNEt_2基团在两个Mo原子间跨桥配位。XPS和Mossbauer谱的测定及M-S(M=Fe或Mo)键长比较表明,簇合物中Fe原子的氧化态是不同的,而两个Mo原子则具有相同的氧化态。该簇合物为顺磁性物质,μ_m=4.27μ_B。此外,还测定了它的红外光谱,紫外-可见光谱和催化乙炔还原活性。

从ITS序列探讨青藏高原特有植物华福花属的亲缘关系(英文)

对青藏高原特有的濒危植物华福花 (SinadoxacorydalifoliaC .Y .Wu ,Z .L .WuetR .F .Huang)的核糖体DNA中的内转录间隔区 (ITS)序列及 5 .8SrRNA基因的序列进行了测定。同川续断目和五加目有关类群序列的比较及分支分析表明华福花属与五福花属 (AdoxaL .)近缘 ,不支持它可能与五加目或败酱科有亲缘关系的假设。尽管形态上它与五福花属分化十分明显 ,但ITS碱基分异却较小。引起其系统位置发生争论的外部形态为什么进化得如此之快 ,是值得进一步深入探讨的课题。