The role of potential structure in excitation functions of synthesizing superheavy nuclei

The excitation functions of two very similar reaction channels, Fe-58+Pb-208 ->(265)Hs+1n and Fe-58+Bi-209 ->(266)Mt+1n are studied in the framework of the dinuclear system conception. The fusion probabilities are found to be strongly subject to the structure of the driving potential. Usually the fusion probability is hindered by a barrier from the injection channel towards the compound nuclear configuration. The barrier towards the mass symmetrical direction, however, also plays an important role for the fusion probability, because the barrier hinders the quasi-fission, and therefore helps fusion.

Characterization of complex hydrocarbons in cigarette smoke condensate by gas chromatography-mass spectrometry and comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry

Gas chromatography-mass spectrometry with electron ionization and positive-ion chemical ionization and comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry (GC x GC-TOF-MS) were applied for the characterization of the chemical composition of complex hydrocarbons in the non-polar neutral fraction of cigarette smoke condensates. Automated data processing by TOF-MS software combined with structured chromatograms and manual review of library hits were used to assign the components from GC x GC-TOF-MS analysis. The distributions of aliphatic hydrocarbons and aromatics were also investigated. Over 100 isoprenoid hydrocarbons were detected, including carotene degradation products, phytadiene isomers and carbocyclic diterpenoids. A total of 1800 hydrocarbons were tentatively identified, including aliphatic hydrocarbons, aromatics, and isoprenoid hydrocarbons. The identified hydrocarbons by GC x GC-TOF-MS were far more than those by GC-MS. (C) 2004 Elsevier B.V. All rights reserved.

Separation of acidic and basic compounds in capillary electrochromatography with polymethacrylate-based monolithic columns

Methacrylate-based monolithic columns with electroosmotic flow (EOF) or very weak EOF are prepared by in situ copolymerization in the presence of a porogen in fused-silica capillaries pretreated with a bifunctional reagent. Satisfactory separations of acidic and basic compounds on the column with EOF at either low or high pH are achieved, respectively. With sulfonic groups as dissociation functionalities, sufficient EOF mobility still remains as high as 1.74 x 10(-4) cm(2) s(-1) V-1 at low pH. Under this condition, seven acidic compounds are readily separated within 5.7 min. Moreover, at high pH, the peak shape of basic compounds is satisfactory without addition of any masking amines into running mobile phase since the secondary interaction between the basic compounds and the monolithic stationary phase are minimized at high pH. Reversed-phase mechanism for both acidic and basic compounds is observed under investigated separation conditions. In addition, possibilities of acidic and basic compound separations on a monolithic column with extremely low EOF are discussed. (C) 2004 Elsevier B.V. All rights reserved.

Heat capacity and enthalpy of fusion of penconazole (C13H15C12N3)

Low-temperature heat capacities of penconazole (C13H15Cl2N3) were precisely measured with an automated adiabatic calorimeter over the temperature rang from 78 to 364 K. The sample was observed to melt at 332.38 +/- 0.06 K. The molar enthalpy and entropy of fusion of the compound were determined to be 33580 +/- 11 J mol(-1), 101.03 +/- 0.02 J mol(-1) K-1, respectively. Further research of the melting process for this compound was carried out by means of differential scanning calorimetry (DSC) technique. The result was in agreement with that obtained from the measurements of heat capacities. (C) 2003 Elsevier B.V. All rights reserved.

Thermodynamic investigation of the azeotropic mixture composed of water and benzene

The molar heat capacity of the azeotropic mixture composed of water and benzene was measured by an adiabatic calorimeter in the temperature range from 80 to 320 K. The phase transitions took place in the temperature range from 265.409 to 275.165 K and 275.165 to 279.399 K. The phase transition temperatures were determined to be 272.945 and 278.339 K, which were corresponding to the solid-liquid phase transitions of water and benzene, respectively. The thermodynamic functions and the excess thermodynamic functions of the mixture relative to standard temperature 298.15 K were derived from the relationships of the thermodynamic functions and the function of the measured heat capacity with respect to temperature.

长白山北坡森林群落交错区优势树种动态(英文)

基于28个20mx90m样地的调查数据,利用Lotka-Volterra模型,本文分析了长白山北坡阔叶红松(Pinuskoraiensis)林和云冷杉林(也叫暗针叶林)群落交错区优势树种之间的竞争及动态。结果显示:在自然条件下,群落将向两个方向分化,一是以云杉(PiceajezoensisandP.koraiensis)和冷杉(Abiesnephrolepis)为优势的群落,并在达到平衡时冷杉占绝对优势(相对优势度的77.1%):另一种是以红松或云冷杉和阔叶树占绝对优势的针阔混交林,并在达到平衡时,阔叶树在阔叶红松林中占相对优势度的50%,在云冷杉一阔叶林类型中占66%。同时,本研究说明:(1)阔叶红松林和云冷杉林都是长白山气候顶极群落:(2)交错区具有过渡性质:(3)森林群落的分化结果说明演替的方向受局部生境的影响。图1表3参24。

长白山北坡植物群落复杂性的海拔梯度变化(英文)

应用梯度格局法在长白山北坡海拔700m-2600m的坡面上每100 m海拔设置一样地,共计20块样地,通过对同一群落各样方间的相异性测定,对各海拔植物群落的复杂性进行了分析。结果表明,以主林层乔木种的二元数据计算的结果,除亚高山岳桦林外,其它各海拔群落的样方间均表现出较高的相异性,特别是低海拔的阔叶红松林平均相异系数达0.74,明显高于其它植被类型;暗针叶林各群落间差异不大,相对而言1400 m群落样方间的相异性略高于其它群落,表现出过渡性群落树种组成的复杂性;岳桦林树种组成简单,样[(\267\275\274\344\322\262\261\355\317\326\263\366\275\317\270\337\265\304\\317\340\313\306\320\324\241\243)-0.1(\322\324\271\340\304\276\326\326\265\304\266\376\324\252\312\375\276\335\\274\306\313\343\265\304\310\272)]落内的相异性,虽低海拔的阔叶红松林总体上高于其它群落,但差异趋势并不像乔木种那么明显。以各草本植物与所有植物种的二元数据计算的各海拔群落内样方间的相异性,表现出非常相近的趋势,群落内样方间草本植物及所有植物种均以阔叶红松林及高山冻原差异最大,暗针叶林基本稳定于比较相近的水平。图3表1参8。

Femtosecond pump-probe mass spectra on the dissociative photoionization of CF3I

The multi-photon dissociative photoionization dynamics of CF3I has been studied with femtosecond two-color pump-probe time-of-flight mass spectra at a pump pulse of 265 nm and a probe pulse of 398 nn. This enables the A band and 5ppi(3)7ssigma((2)Pi(1/2)) Rydberg state to be accessed with the pump beam. The observed fast and slow decay components of CF3+ and I+ reflect the fast repulsive A band and some higher lying ion-pair states may be responsible for the decay of the 5ppi(3)7ssigma((2)Pi(1/2)) Rydberg state. The results provide information on the different multi-photon pathways producing these ions and the de-excitation mechanism of the 5ppi(3)7ssigma((2)Pi(1/2)) Rydberg state. (C) 2003 Elsevier Science B.V. All rights reserved.

大兴安岭北坡火后紫貂冬季生境恢复研究(英文)

由自然和人为原因引起的生境丧失与生境破碎化已严重影响到野生动物的生存。大兴安岭北坡是国家一级保护动物紫貂(Marteszibellina)的主要分布区,1987年发生在这里的特大森林火灾造成了森林景观的严重破碎化,紫貂的生存面临极大的威胁。本文的研究目的是为了确定火灾13年后,紫貂冬季生境的恢复程度。首先根据紫貂对冬季生境的喜好选取对其生存影响较大的生态因子,结合数字化林相图,利用地理信息系统软件ArcGIS编制火烧前后的生境适宜性类型图。然后选取相关的景观格局指标,对火灾烧前后的生境格局进行对比分析。结果显示:尽管火后采取了一系列的森林恢复措施,但紫貂冬季适宜生境仍有大幅度减少,特别是中等适宜生境类型减少最为明显。适宜生境破碎化加剧,隔离度增加。适宜生境斑块的形状趋于简单,软边界比重有所增加。以上结果表明,与火前相比,紫貂生境明显恶化,需要较长的时间恢复。图4表5参41。

ZnO clusters encapsulated inside micropores of zeolites studied by UV Raman and laser-induced luminescence spectroscopies

Using microporous zeolites as host, sub-nanometric ZnO clusters were prepared in the micropores of the host by the incipient wetness impregnation method. A small amount of sub-nanometric ZnO clusters were introduced into the channels of HZSM-5 zeolite, whereas a large quantity of sub-nanometric ZnO clusters can be accommodated in the supercages of HY zeolite and no macrocrystalline ZnO exists on the extra surface of the HY material. The vibrations of the zeolite framework and ZnO were characterized by UV Raman spectroscopy. The optical properties of these ZnO clusters were studied by UV-visible absorption spectroscopy and laser-induced luminescence spectroscopy. It is found that there are strong host-guest interactions between the framework oxygen atoms of zeolite and ZnO clusters influencing the motions of the framework oxygen atoms. The interaction may be the reason why ZnO clusters are stabilized in the pores of zeolites. Different from bulk ZnO materials, these sub-nanometric ZnO clusters exhibit their absorption onset below 265 nm and show a purple luminescence band (centered at 410-445 nm) that possesses high quantum efficiency and quantum size effect. This purple luminescence band most likely originates from the coordinatively unsaturated Zn sites in sub-nanometric ZnO clusters. On the other hand, the differences in the pore structure between HZSM-5 and HY zeolites cause the absorption edge and the purple luminescence band of ZnO clusters in ZnO/HZSM-5 show a red shift in comparison with those of ZnO clusters in ZnO/HY.