超重核合成时的驱动势与热熔合反应截面

在双核模型框架下,双核系统生成超重复合核的机理是由双核中的弹核的核子全部转移到靶核产生的,而核子转移是由双核系统驱动势确定的.对有的反应道,核子转移与中质比变化路径之间有比较复杂的关系.原则上动力学方程与驱动势都应该是中子和质子的二维显函数.为处理方便,采用与中质比相关的核子转移路径的选择来取驱动势,得到了接近实验值的超重核合成蒸发剩余截面.

The driving potential and cross sections for synthesizing super heavy nuclei with hot fusion

The dinuclear model of the formation mechanism of a superheavy compound nucleus assumes that when all nucleons of the projectile have been transferred in to the target nucleus the compound nucleus is formed. The nucleon transfer is determined by the driving potential. For some reaction channels, the relation between nucleon transfer and the evolution path of the neutron/proton ratio is rather complicated. In principle, both the dynamical equation and the driving potential should be a twodimensional explicit function of the neutron and proton. For the sake of simplicity we calculated the driving potential by choosing the path of the nucleon transfer which is related to the nutron/proton ratio, and the calculated evaporation residue cross-sections to synthesize the superheavy nuclei are much closer to the experimental data

Decay dynamics of excited CS2 and NH3 investigated by femtosecond laser

By using the home-made femtosecond laser system and the time-of-flight mass spectrometer, the decay dynamics of excited carbon disulfide (CS2) and ammonia (NH3) are investigated in real time by pump-probe multiphoton ionization detection. The estimated lifetime constant of the NH3 (A) over tilde (1)A(2)' state (51+/-4 fs) agreed quite well with the literature report. For the first time, the decay lifetime constants of the NH3 (E) over tilde'(1)A(1)' state (937+/-93 fs), the CS2 (a) over tilde (3)A(2) state (153+/-10 fs), and the CS2 Rydberg state [(3)/(2)]6ssigma(g) ((3)Pi(g)) (948+/-23 fs) are obtained.

人工小叶锦鸡儿(Caraganamicrophylla)灌丛土壤水分动态研究

采用由植被空间序列推断时间系列的方法 ,分析了 1984、1987、1995和 1999年建立的人工小叶锦鸡儿固沙植被土壤水分的时空变化特征 .结果表明 ,受沙地土壤机械组成的影响 ,沙地土壤组成以物理性沙粒为主 ,>0 .0 1mm沙粒占 97%以上 ,凋萎湿度为 1.5 5 % ,田间持水量为 5 .5 % ,土壤最大有效水为3.95 % .随着固沙植被优势度的增加 ,小叶锦鸡儿灌丛下土壤含水量持续下降 ,1984年建立的植被区土壤含水量明显低于 1999年建立的植被区 ;在年内土壤水分季节变化中 ,4个阶段植被区土壤水分状况在 4～6月不断降低 ,到 6月达到最低值 ,7～ 10月逐渐回升 ;对于建立较早的植被区 (1984和 1987年 ) ,土壤水分垂直变化表现出随着土层深度的增加 ,土壤含水量逐层递减的趋势 ,特别是 70cm下土层中 ,土壤含水下降明显 ,含水量低于凋萎湿度 ;由于对根际区域土壤水分的利用 ,加剧了固沙植被区深层土壤 (70cm下 )水分的亏缺 ,进而影响植被物种的组成 ,随着小叶锦鸡儿灌丛年龄的增加 ,浅根性植物所占比重增加 .

潭江流域森林碳储量及其动态变化

根据森林碳储量的计算方法和森林资源清查资料,结合实地调查校正,估算了11年来快速城市化过程中潭江流域森林的碳储量及其动态变化,分析了人口密度、GDP增长与森林的碳储量、碳密度的相关关系.结果表明,潭江流域森林碳储量由1990年的5.906×106t增长到2001年的7.852×106t,年均增长0.18×106t,增长率为3.05%,起到了碳汇的作用.人口密度的增加和经济的快速发展没有影响到森林碳储量和碳密度的增加,但林业发展速度远落后于经济发展的速度.合理的林业管理模式与经济发展相互协调是流域森林生态系统在城市化过程中提供更好的服务功能并促使区域生态环境可持续发展的关键.

Chiral ligand 2-(2 '-piperidinyl)pyridine: synthesis, resolution and application in asymmetric diethylzinc addition to aldehydes

Chiral ligand 2-(2'-piperidinyl)pyridine 1 has been synthesized in good overall yield by sequential benzylation, hydrogenation and debenzylation of 2,2'-bipyridine. Its enantiomerically pure enantiomers have been obtained by resolution of 2-(1-benzyl-2-piperidinyl)pyridine 2 with D-tartaric acid (or L-tartaric acid) followed by debenzylation. The absolute configuration was determined by X-ray analysis of the (S)-2 D-tartrate. It was demonstrated that I can be used as an effective enantioselective catalyst in the addition of diethylzinc to aldehydes.

Hydrothermal synthesis, structure characterization of a new mixed Mo/V metal-oxygen cluster compound: [Co(phen)(3)](2)[HPMo4V (Mo4V6IV)-V-VI M2O44]center dot 4H(2)O, (M=0.78Mo(V)+0.22V(IV))

A new polyoxometalate [Co(phen)(3)](2)[HPMo4V Mo-4(VI) V-6(IV) M2O44]center dot 4H(2)O (M = 0.78Mo(V)+ 0.22V(IV)) 1 was hydrothermally synthesized and characterized by IR, elemental analyses, X-ray photoelectron spectrum, ESR and single crystal X-ray diffraction. The title compound is in the triclinic space group P (1) over bar with a = 12.0953(7) angstrom, b = 14.0182(6) angstrom, c = 14.6468(7) angstrom, V=2402.55(18) angstrom(3), alpha = 105.134(2), beta = 91.841(3), gamma = 91.401(2), Z = 1, and R-1 (wR(2)) = 0.0617 (0.1701). The compound was prepared from tetra-capped pseudo-Kepin with phosphorus-centered polyoxoanions [PMo8V6M2O44](5-) , [Co(phen)(3)](2+) cations and linked through hydrogen bonds and pi-pi stacking interaction into three-dimensional supramolecular framework. Astudy of the magnetic properties of 1 demonstrates that it exhibits antiferromagnetic coupling interactions.

Determination of ascorbic acid by flow injection chemiluminescence suppression method

chemiluminescence suppression method for the determination of ascorbic acid based on Luminol-KIO4-H2O2-ascorbic acid system was established. The linear range for ascorbic acid is 1.0 x 10(-7) similar to 1.0 x 10(-5) mol/L and the detection limit is 6.0 x 10(-8) mol/L. The relative standard deviation (n = 11) is 1.0% for 8.0 x 10(-7) mol/L ascorbic acid. The method has been used to determine the content of ascorbic acid in tablets and injections with satisfactory results.

流动注射化学发光抑制法测定抗坏血酸

基于抗坏血酸对Ｌｕｍｉｎｏｌ－ＫＩＯ４－Ｈ２Ｏ２体系化学发光反应的抑制作用，建立了化学发光抑制快速测定抗坏血酸的新方法。该方法线性范围为 １．０ × １０－７～ １．０ × １０－５ ｍｏｌ／Ｌ，检出限为６．０× １０－８ｍｏｌ／Ｌ，对８．０× １０－７ｍｏｌ／Ｌ抗坏血酸 １１次平行测定的相对标准偏差为 １．０％。用于维生素Ｃ片剂及注射液中抗坏血酸含量的测定，结果令人满意。

The electrical and magnetic properties of lanthanide alkaline-earth transition-metal oxides

Five Ln(2)SrMCuO(6.5) oxides (M = Co, Ln = Y and Ho; M = Fe, Ln = Y, Ho, and Dy) were synthesized, and their crystal structures, IR spectra, and physical properties were studied. They have almost the same structure and crystallize in orthorhombic systems. Below room temperature, Y2SrFeCuO6.5, a known layered oxide, shows antiferromagnetic behavior, but the four new oxides are paramagnetic. Y2SrFeCuO6.5 fits the Curie-Weiss law in the temperature range 300-100 K, but Y2SrCoCuO6.5 shows complex magnetic behavior because of the disproportion of some Co+3 to Co+2 and Co+4 The five oxides are all p-type semiconductors in the measured temperature range and have large electrical resistivities at room temperature.

Effects of molecular weight and interaction parameter on the glass transition temperature of polystyrene mixtures and its blends with polystyrene/poly(2,6-dimethyl-p-phenylene oxide)

The glass transition temperature (T-g) of mixtures of polystyrene (PS) with different molecular weight and of blends of poly(2,6-dimethyl-p-phenylene oxide) (PPO) and polystyrene with different molecular weight (DMWPS) was studied by a DSC method. For the whole range of composition, the curves of T-g vs composition obtained by experiment were compared with predictions from the Fox, Gordon-Taylor, Couchman and Lu-Weiss, equations. It was found that the experimental results were not in agreement with those from the Fox, Gordon-TayIor and Couchman equations for the binary mixtures of DMWPS, where the interaction parameter chi was approximately zero. However, for the blends PPO/DMWPS (chi < 0), with an increase of molecular weight of PS, it was shown that the experimental results fitted well with those obtained from the Couchman, Gordon-Taylor and Fox equations, respectively. Furthermore, the Gordon-Taylor equation was nearly identical to the Lu-Weiss equation when \chi\ was not very large. Further, the dependence of the change of heat capacity associated with the glass transition (Delta C-p) on the molecular weight of PS was investigated and an empirical equation was presented. (C) 1997 Elsevier Science Ltd.

Ionic conductivity of polymer gel electrolytes based on poly(polyethylene glycol dimethacrylate)

Gel electrolytes have been prepared by thermal polymerization of poly(polyethylene glycol dimethacrylate) (P(PEGD)) in the presence of propylene carbonate (PC) and alkali metal salts, such as LiClO4, LICF(3)SO(3) and LiBF4. The conductivity was studied by means of impedance spectroscopy, and it is found that the temperature dependence of conductivities follow a Arrhenius relationship when the molar percentage of PC is higher than 75% or LiClO4 concentration is lower than 0.9 mol/l. However, when LiCF3SO3 or LiBF4 is used instead of LiClO4 as the salt, the situation is different. For LICF(3)SO(3), the Arrhenius relationship almost holds true for all the salt concentrations studied; while for LiBF4, the Arrhenius equation hardly fits for any salt concentration. The dependence of activation energy on salt concentration is also examined, both for LiClO4 and LiCF3SO3, the values of E(a) tend to reach a minimum value with increasing salt concentration. Copyright (C) 1996 Elsevier Science Ltd.