PROJECTILE FRAGMENTATION OF Ar-36,Ar-40 INDUCED REACTIONS

Fragment yields for Z >= 5 from projectile fragmentation using primary beams of Ar-36,Ar-40 at 50 MeV/nucleon on Ni-64 target have been measured in RIBLL fragment separator. We compare the fragment cross sections with the predictions of the empirical EPAX parametrization of fragmentation cross-sections and Statistical Abration-Ablation model (SAA) by considering the RIBLL separator transmission rate. Isotope yield ratios between these two reactions were calculated and isoscaling parameters alpha and beta are extracted, their dependences on fragment atomic number Z and neutron number N were presented.

30MeV/u~(40)Ar引起反应中的碎片发射机制

本论文中重点研究了30MeV/u 40Ar+58Ni，64Ni和115In反应中中等质量碎片（IMF）的发射机制。实验中，测量了实验室系5°～140°角度范围内出射碎片的能谱和角分布。对前角区出射的IMF（3≤Z≤13）实现了同位素鉴别，对中后角区出射的碎片在低探测阈（<2MeV/u ）的前提下实现了直到Z～30的元素鉴别。 用运动源模型对不同角度下出射的碎片能谱进行了分析和讨论，并结合角分布特征定性地研究了碎片的三个发射源。通过对各源的贡献随角度以及出射碎片电荷数Z的演化，观察到：类弹源主要发射的是那些前角区出射的、接近束流速度的高能碎片；中等速度源的发射是中角度区出射碎片和前角区低能碎片的主要来源；后角区出射的碎片则主要来自于类熔合源的发射。并观察到相对于类熔合源非平衡源更容易发射较轻的碎片。 通过对前角区出射IMF（3≤Z≤13）的能谱和同位素分布的分析，确定了那些基本保持束流速度的碎片主要来自于弹核碎裂过程。用各种模型对实验同位素分布进行了拟合，发现Sümmerer等人给出的经验公式和abrasion-ablation模型均能比较满意地拟合实验同位素分布的宽度和峰位。同时也观察到abrasion-ablation模型计算对奇Z元素的同位素分布能给出较好的拟合，但对偶Z元素的同位素分布，计算结果与实验值相比出现向丰中子方向的系统性偏移（～lamu）。另外，还着重研究了这些产物的靶核相关性问题。通过系统性分析以及同位旋相关的量子分子动力学（IQMD）模型计算，得出了弹核碎裂产物的靶核相关性是源于靶核表面中子与质子分布的不同和平均场及核子核子相互作用的同位旋效应相关。并且，通过计算还指出了靶核中子皮的厚度对于用弹核碎裂方法产生丰中子同位素的重要性。 通过用统计模型拟合后角区出射碎片的电荷分布，指出了这些碎片主要来自于非完全熔合过程中形成的复合系统的统计发射。 实验中观察到30MeV/u 40Ar轰击Ni和In靶在中角区出射的碎片的电荷分布有不同的特征。相对来说，前者更服从power-law，后者则倾向于服从指数规律。结合核态方程和QMD模型计算分析得出，在30MeV/u 的40Ar引起的反应中，对于弾靶质量接近对称的碰撞对所形成的系统，在一定的碰撞条件下可能已进入spinodal区，而非对称碰撞对的碰撞中压缩能还难以使得系统在膨胀时进入力学不稳定区。从而对观察到的实验现象进行了说明，并认为30MeV/u 40Ar轰击与其质量接近的靶核的反应中出射的碎片中已有相当数量的动力学发射成分的贡献。 利用实验中在前角区出射的接近束流速度的碎片的同位素产额提取了类弹源的温度参数。观察到直接由实验同位素产额比得到的表观核温度与所选择的同位素组合有较强烈的依赖关系，而与靶核和实验室探测角基本无关。利用M.B.Tsang等人给出的修正方法，提取了经边馈效应修正后的发射源温度。得到该温度值与反应靶、探测角以及用于提出温度的同位素组合没有明显的依赖关系，均为～4MeV。并用abrasion-ablation模型计算进行了讨论，得到在假定能级密度参数的倒数k=10MeV时，该温度值与abrasion-ablation模型计算是一致的。

Photo-induced reactions in the ion-molecule complex Mg+-OCNC2H5

Ion - molecule complexes of magnesium cation with ethyl isocyanate were produced in a laser- ablation supersonic expansion nozzle source. Photo- induced reactions in the 1: 1 complexes have been studied in the spectral range of 230 - 410 nm. Photodissociation mass spectrometry revealed the persistent product Mg+ from nonreactive quenching throughout the entire wavelength range. As for the reactive channels, the photoproducts, Mg+OCN and C2H5+, were produced only in the blue absorption band of the complex with low yields. The action spectrum of Mg+(OCNC2H5) consists of two pronounced peaks on the red and blue sides of the Mg+ 3(2)P <-- 3(2)S atomic transition. The ground state geometry of Mg+ - OCNC2H5 was fully optimized at B3LYP/6- 31 - G** level by using GAUSSIAN 98 package. The calculated absorption spectrum of the complex using the optimized structure of its ground state agrees well with the observed action spectrum. Photofragment branching fractions of the products are almost independent of the photolysis photon energy for the 3P(x,y,z) excitations. The very low branching ratio of reactive products to nonreactive fragment suggests that evaporation is the main relaxation pathway in the photo- induced reactions of Mg+ (OCNC2H5). (C) 2003 American Institute of Physics.

Fabrication and characterization of self-doped poly (aniline-co-anthranilic acid) nanorods in bundles

Poly (aniline-co-anthranilic acid) (PANANA) nanorods in bundles was prepared successfully in an alcohol/aqueous media without assistance of an), other kinds of acids. Anthranilic acid played all roles of monomer, acid-media provider, and dopant in the reaction system, and ammonium persulfate (APS) served as the oxidant. The morphologies of PANANA nanorods in bundles were investigated by scanning electron microscopy (SEM). Influences of the monomer molar ratio on the resulting morphology were investigated. Moreover the formation mechanism of the nanostructured copolymer was proposed. FT-IR. UV-vis and X-ray diffraction (XRD) measurements were used to confirm the molecular and electrical structure of the self-doped PANANA. The intrinsic properties, such as conductivity, electrochemical redox activity and room-temperature solubility of the resulting copolymer were explored.

Novel < 110 >-oriented organic-inorganic perovskite compound stabilized by N-(3-aminopropyl) imidazole with improved optical properties

In the organic-inorganic perovskites family, the < 100 >-oriented type has been extensively investigated as a result of its unique magnetic, optical, and electrical properties, and only one type of < 110 >-oriented hybrid perovskite stabilized by methylammonium and iodoformamidinium cations or the latter themselves has been known so far. In this paper, another novel < 110 >-oriented organic-inorganic perovskite (C6H13N3)-PbBr4 (compound 1) has been prepared by reacting N-(3-aminopropyl)imidazole (API) with PbBr2 in hydrobromic acid. The crystal structure is determined, which indicates that the perovskite is stabilized by API. The introduction of the optically active organic ligand API into the hybrid perovskite results in a red shift and a great enhancement of photoluminescence in the perovskite with respect to organic ligand API itself. These results have been explained according to calculation based on density-functional theory. Moreover, the excellent film processing ability for the perovskite (C6H13N3)PbBr4 together with the improved optical properties makes it have potential application in optoelectronic devices.

Determination of Nb and Ta in Nb/Ta minerals by inductively coupled plasmas optical emission spectrometry using slurry sample introduction

The determination of Nb and Ta in Nb-Ta minerals was accomplished by slurry nebulization inductively coupled plasma optical emission spectrometry (ICP-OES), using a clog-free V-groove ceramic nebulizer. Samples were first wet-ground to appropriate particle sizes with narrow size distribution and 90% of the particles in the slurry were smaller than 2.32 mu m in diameter. Subsamples were then dispersed in pH 9 aqueous solutions, and agitated in an ultrasonic bath for 15 min prior to analysis. Due to the lack of slurry standards matching well with the samples, calibration was simply carried out using aqueous solution standards. Results were compared with those obtained from a conventional fusion decomposition procedure and acid digestion procedures and a good agreement between the measured and referred values was obtained. The technique provided a good alternative for the rapid determination of Nb and/or Ta in their corresponding minerals.

Degradation of polyimide induced by nitrogen laser irradiation

The degradation behavior of polyimide (PMDA-ODA) induced by nitrogen laser irradiation was studied. The changes in the surface morphology and the composition of the irradiated polyimide films were examined by scanning electron microscopy, X-ray photoelectron spectroscopy and FT-IR spectroscopy. The initial reaction was achieved by photochemical degradation of polyimide in the highly electronic excited state by the absorption of a second 337 nm photon. Atmospheric oxygen sequentially reacted with the produced radicals to form a highly oxidized layer. The formation of carbonyl group was enhanced by the heat remaining on the irradiated polyimide film surfaces. (C) 2000 Elsevier Science B.V. All rights reserved.

Formation of conducting layers on excimer-laser-irradiated polyimide film surfaces

Conducting layers on KrF excimer-laser-irradiated polyimide film surfaces were investigated by XPS, SEM and Fourier transform infrared (FTIR)-Raman spectroscopy, Analysis of polyimide residue after laser irradiation provided valuable insight into the nature of the formation of conducting layers. The subtle different between KrF laser irradiation and the pyrolysis of polyimide was found by comparison of the formation process of conducting layers. A physical picture was presented to describe better the formation of conducting layers. Under KrF laser irradiation, polyimide films underwent thermal decomposition assisted by photoinduced direct bond breaking. Polycrystalline graphite was subsequently formed as the product of the secondary addition reaction of carbon-enriched clusters, Such reaction was supported by the remaining energy on the irradiated polyimide film surface. This result shows that the thermal process played an important role that was not just restricted to the formation of conducting layers, Copyright (C) 2000 John Wiley & Sons, Ltd.

Thermal influence on excimer-laser-induced electrical conductivity on polyimide film surfaces

The thermal influence on the electrical conductivity of polyimide film surfaces induced by KrF-laser irradiation was investigated, The formation of conducting phases was demonstrated to be highly temperature sensitive, as evidenced by strong dependence of the electrical conductivity on repetition rate and ambient temperature. XPS and Raman studies showed that the efficiency of the formation of conducting phases could be enhanced by the increase of temperature on irradiated polyimide film surfaces. After the disruption of polymeric chain, the carbon-enriched clusters remained on the irradiated polyimide film surfaces organized into polycrystalline graphite-like clusters responsible for electrical conductivity. The resulting dangling bonds from the decomposition process of polyimide acted as centers for the rearrangement of carbon-enriched clusters. It is suggested that the motion of radicals was promoted with increasing the temperature. Therefore the formation of polycrystalline graphite-like clusters benefited from high remaining temperature on the irradiated polyimide film surfaces. These results revealed that thermal influence played a dominant role on the formation of conducting phases.

Trace analysis of Zn-doped compound semiconductor material by resonant ionization mass spectrometry

An experimental setup and the procedure for the laser resonant ionization mass spectrometry (RIMS) have been described. Both an optical spectrum and a mass spectum have been shown. The detection limit that can be reached by using this procedure has been estimated.

东南极格罗夫山地区的陨石回收与研究

Chinese National Antarctic Research Expedition (CHTNARE) has collected 4480 meteorite specimens in the Grove Mountains, East Antarctica, from 1998 to 2003. According to the location characteristics and the diversity of the classification, the paper concludes that the Grove Mountains is another important meteorite concentration area in the Antarctica. The Concentration mechanisms at the site could be related to the last glacier activity and katabatic wind. An empirical model was proposed: 1) Probably during the Last Glacial Maximum, ice flow overrided the Gale Escarpment range in the area. Formerly concentrated meteorites were carried by the new glacier and stayed in the terminal moraine when the glacier retreated. 2) Blown by strong katabatic wind, Newly exposed meteorites on the ablation zone were scattered on the blue ice at the lee side of the Gale escarpment. Some of them would be buried when they were moved further onto the firn snow zone. Many floating meteorites stopped and mustered at the fringe of the moraine. The chemical-petrographic of 31 meteorites were assigned based on electron probe microanalyses, petrography and mineralogy, including 1 martian lherzolitic shergottite, 1 eucrite, 1 extreme fine grain octahedron iron meteorite, and 28 ordinary chondrites (the chemical groups: 7 H-group, 13 L-group, 6 LL-group, 2 L/LL group; the petrographic types: 6 unequilibrated type 3 and 22 equilibrated type 4-6). GRV99028 meteorite has the komatiite-like spinifex texture consisting of acicular olivine crystals and some hornblende-family minerals in the interstitial region. Possibly it has crystallized from a supercooled, impact-generated, ultramafic melt of the host chondrite, then experienced the retrogressive metamorphism. Four typical chondrule textures were studied: porphyritic texture, radiative texture, barred texture and glass texture. The minerals are characteristically enriched in MgO content.