Qβ measurements of 158, 159Pm , 159, 161Sm , 160-165Eu , 163Gd and 166Tb using a total absorption BGO detector

Q _β values of the neutron-rich isotopes of ^160-165Eu and ¹⁶³Gd were measured for the first time using a total absorption bismuth germanate (BGO) detector, and previously obtained data on ^{158, 159}Pm , ^{159, 161}Sm and ¹⁶⁶Tb were re-analyzed. These radioactive sources were prepared by an on-line mass separator (Tokai-ISOL) following the ²³⁸U (p,f reaction. The deduced Q _β values are the following: 6085(80)keV for ¹⁵⁸Pm , 3805(65)keV for ¹⁵⁹Sm , 5460(140)keV for ¹⁵⁹Pm , 4705(60)keV for ¹⁶⁰Eu , 5065(130)keV for ¹⁶¹Sm , 3705(60)keV for ¹⁶¹Eu , 5575(60)keV for ¹⁶²Eu , 4690(70)keV for ¹⁶³Eu , 3170(70)keV for ¹⁶³Gd , 6430(70)keV for ¹⁶⁴Eu , 5800(120)keV for ¹⁶⁵Eu , and 4695(70)keV for ¹⁶⁶Tb . Moreover, the deduced mass excesses and two-neutron separation energies ( S _2n values) were compared with those of the atomic mass evaluations and theoretical predictions.     

Gas phase interaction of L‐proline with Be2+, Mg2+ and Ca2+ ions: a computational study

Geometry optimisation and metal ion affinities (MIAs) of the binding configurations of Be²⁺, Mg²⁺ and Ca²⁺ to L ‐proline were calculated using the hybrid Density Functional Theory (DFT‐B3LYP) and second order Møllet?Plesset perturbation theory (MP2) methods. Be²⁺ was found to bind preferentially in a charge transfer type arrangement through the carbonyl oxygen (? C?O) and the lone pair of the imino‐group nitrogen atom (? NH? ). On the contrary Mg²⁺ and Ca²⁺ were found to prefer binding in a bi‐dentate manner through the carboxylate group of L ‐proline (OCO) in a zwitterion form. The main types of interactions found to influence the binding preference of M²⁺ ions to L ‐proline were (i) charge transfer in the case of Be²⁺ ions and (ii) electrostatic interactions in the case of Mg²⁺ and Ca²⁺ ions. Inspection of the IR stretching of the N? H and the O? H groups of L ‐proline with M²⁺ ions in a chelating configuration (to both O and N atoms) indicated a considerable shift to higher frequency with decreasing MIA. On the other hand, the MIA for the zwitterion L ‐proline with M²⁺ tracks the reciprocal distance of the M²⁺? OCO bond further confirming that the nature of the bond is mainly electrostatic. Comparison with other molecules containing the carboxylic function is also included in order to gain more insight on the types of interaction of this amino acid with metal ions in general. Copyright © 2007 John Wiley & Sons, Ltd.     

New type of biosensor based on magnetic nanoparticle detection

A new type of biosensor has been developed based on detection of nanosized superparamagnetic particles that serve as labels in bioreactions. The method is based on non-linear magnetic material detection by a magnetic field having components at two frequencies f₁ and f₂. The response is measured at the combinatorial frequencies f_i=mf₁+nf₂, where m and n are integers, e.g., f_i=f₁±2f₂. Several highly sensitive readers of superparamagnetic particles have been designed and used for development of various formats of immunoassays, including those compatible with immunoconcentration and magnetic enrichment of antigens.     

Fluram labeling of high density NH2 surfaces

Some surface bonded and fluram labeled primary amines show a new red-shifted emission in their fluorescence spectrum. We compared the fluorescence of fluram bonded to various amine functionalized surfaces including tetraethylene pentamine (TEPA), 1,2-ethylene diamine (EDA), 3-aminopropyltriethoxy silane (APTES) and trimetylol-propanetris-(beta-aziridino)-propionate (ATA). All reactions were also monitored using XPS. It was found that the new spectral features seem to be related to the local density of amino groups on the surface. In order to verify this hypothesis we synthesized a surface bonded dendrimer with a step-wise increasing NH₂ density. Using molecules with different lengths as branches in the dendrimer, the amine density can be varied. Only in the case of the highest density, the new fluorescence emission was detected. Consequently, the fluorescence of fluram coupled to amines at a surface can be used to quantify the concentration of these amines and the appearance of the red-shifted emission indicates a high local density of the amino groups.     

A non-thermal chemical synthesis of hydrophilic and amorphous cobalt oxide films for supercapacitor application

Present work explored a room temperature, simple and low cost chemical route for the preparation of hydrophilic cobalt oxide films from alkaline cobalt chloride (CoCl₂:6H₂O) and double distilled water precursor solutions. As-deposited cobalt oxide films showed amorphous nature, which is one of the prime requirements for supercapacitor, as confirmed from X-ray diffraction studies. Changes in direct band gap energy and electrical resistivity of as-deposited cobalt oxide films were confirmed after annealing. Spherical grains of about 40-50 nm diameters were uniformly distributed over the substrate surface. Surface wettability studied in contact with liquid interface, showed hydrophilic nature as water contact angle was <90°. Finally, presence of cobalt-oxygen covalent bond was observed from Raman shift experiment.     

The freeze of intrapulse Raman scattering effect of ultrashort solitons in optical fiber

The effect of intrapulse Raman scattering (IRS) for the propagation of the femtosecond solitons in an optical fiber is investigated. To factually simulate its influence, a combination of 27 Lorentian lines to fit experimental Raman gain profile is adopted. By using nonlinear Schrödinger equation and finite-difference time domain method, the propagations of femtosecond fundamental solitons in an optical fiber are numerically calculated. When the initial power is suitably enhanced, it is found that the pulse shape is almost the same as initial pulse and the delay Raman response only makes small pulse shift. In other words, when ultrashort soliton is considered, the IRS effect is similarly frozen under the enhanced initial power.     

中国散裂中子源RFQ的热分析

射频四级场(RFQ)加速器的水冷具有以下两种功用: 首先它可以把射频场发热带走, 维持RFQ腔的热稳定性及限制RFQ强体形变幅度; 其次, 当RFQ失谐时, 它还可以用来进行RFQ的调谐, 而同时又基本不影响RFQ的射频场分布. 由于RFQ粒子的传输效率对射频场的分布极其敏感, 在RFQ的运行中不再采用传统的用调谐器对RFQ进行调谐的方法. 本文通过热分析, 确定了RFQ加速器的水冷管道的数量和布局及最佳工作水温; 确定了RFQ失谐时, 如何利用水温变化来对RFQ进行调谐的方法.     

In situ calibration of a Michelson type, speckle-shearing interferometer: Wobbling mirror effect

In situ calibration of piezoelectric transducers in a phase stepping, Michelson type, speckle-shearing interferometer can be affected by mirror wobbling introduced by the transducers. When this happens, a modulation of the curves employed for calibration can be readily detected in imaging systems with large apertures. A calibration method that takes into account the modulation of these curves is, therefore, essential to insure the required regularity of the phase steps. A computer model of speckle-shearing interferometry is used to deal with piezoelectric non-linearities and mirror wobbling in the interferometer, and to show how the calibration curves are affected when both phenomena are present. Computer simulated and experimental results validate the calibration technique advanced here.     

摆动式声多普勒效应实验仪

针对现有的声多普勒效应实验装置中存在的问题,设计并制作了摆动式声多普勒效应实验仪.该仪器能够分别进行声源运动和观察者运动的声多普勒效应实验,且可定量分析频偏和测量速度.本文详细介绍了该仪器的原理、构造、特点和实验过程,并对实验结果进行了较为全面的分析.     

非线性频率吸引系统的同步动力学

考虑振幅效应的Kuramoto模型,当振子之间存在耗散耦合和非线性频率吸引时,系统展示了丰富的动力学行为.数值分析了最近邻耦合系统的同步动力学行为,相同步和耗散耦合与非线性频率吸引之间的关系,非线性频率吸引对于多于2个振子的系统的同步具有促进作用.