Quantum teleportation of one－ and two－photon superposition states

Quantum teleportation of one- and two-photon superposition states based on EPR entanglement of continuous-wave two-mode squeezed state is discussed. The fidelities of teleportation axe deduced for two different input quantum states. The dependence of the fidelity on the parameters of EPR entanglement and the gain of the classical channels are shown numerically. Comparing with the teleportation of Fock state and coherent state, it is pointed out that for given EPR entanglement and classical gain, the higher the nonclassicality of the input state, the lower the accessible fidelity of teleportation.     

反相非水乳液法制备聚酰亚胺微球

在N,N-二甲基甲酰胺(DMF)/Pluronic-F127、十二烷基苯磺酸钠(SDBS)/液体石蜡(LP)反相非水乳液体系中,以均苯四甲酸二酐(PMDA)和4,4′-二氨基二苯醚(ODA)为单体合成聚酰胺酸(PAA),采用吡啶/乙酸酐脱水剂,对PAA化学酰亚胺化,并进一步热酰亚胺化,制得PI耐热微球.产物通过红外、热重、扫描电镜表征.结果表明,较高的固含量和良好的乳液分散性有利于PI微球的形成;反相非水乳液体系稳定的配比条件是,VDMF∶VLP为1∶4,MF127∶MSDBS为3:2,乳化剂用量为9 wt%;在此配比条件下,当固含量为20%,热酰亚胺化温度不高于330℃时,可制得分散良好、球形规整、高热稳定性的PI微球,其粒径约为10μm.     

Mass transfer in shell-core inorganic TIP1 ion exchanger

The ion exchange processes of (OAc^–) and (OAc^–) proceeding in shell-core inorganic ion exchanger Ti (HPO₄)₂·1/2H₂O has been studied and the diffusion equation whose boundary conditions are satisfied by a shell-core model was solved. Based on the equation solved and experimental data, the diffusion coefficients corresponding to the exchange process (OAc^–) and Li⁺–H⁺ (OAc^–) at 17°C are found to be 7.7×10^–9 and 6.2×10^–8 cm² s^–1 and the activation energies 3.4×10⁴ and 5.0×10³ J mol^–1, respectively. Compared to the gel type of styrene-divinylbenzene strong acid exchanger with 20% cross linking, it can be concluded that the rate of or exchange is 3.5 times faster than that in the organic exchanger.TIP was obtained from the Salt Lake Institute of the Academy of Science of China.     

Wave propagation across a finite heterogeneous interphase modeled as an interface with material properties

Mechanical problems involving an interphase between two well-defined, and eventually different, materials are of interest. The aim of this paper is to present a simplified model that, for low frequency regime, is appropriate for this situation: an interface model with elastic and inertial properties. We present, together with the equations of motion, an identification procedure that is valid for any mass density profile along the thickness of the interphase. For evaluating the accuracy of the model, computations of the reflection coefficients in some relevant cases are shown. Besides, a finite element method is used as a benchmark for both the high and low frequency regimes. It is worth to be noted that the numerical test has been inspired by the problem of the interphase that is formed at the bone-implant boundary.     

Synthesis and characterization of triarylsulfonium salts as novel cationic photoinitiators for UV-photopolymerization

Research on Chemical Intermediates - Using diaryliodonium salts as the arylating reagent and copper as a catalyst, a series of triarylsulfonium salts bearing benzoyl or benzoheterocyclic moieties...     

Liquid hydridosilane precursor prepared from cyclopentasilane via sonication at low temperatures without the action of light

We report on a liquid hydridosilane precursor ink prepared via the ultrasonically induced ring-opening polymerisation of cyclopentasilane (Si₅H₁₀) without irradiation by ultraviolet light. The sonication is carried out in N₂ atmosphere at temperatures between 20 and 75 °C. We use size exclusion chromatography (SEC) to show polymer growth and estimate molecular mass with increasing sonication time. In combination with UV–vis transmission measurements, further SEC analysis is used to compare solutions subjected to either purely thermal or ultrasonic treatment at the same process temperature and for the same duration. Our findings provide strong evidence showing that the initiation of the polymerisation is sonocatalytic in nature and not thermic due to the macroscopic temperature of the solution. The liquid precursor is used to produce homogeneous hydrogenated amorphous silicon (a-Si:H) thin films via spin coating and pyrolytic conversion. The optoelectronic properties of the films are subsequently improved by hydrogen radical treatment. Fourier transform infrared spectroscopy (FTIR) is used to determine a compact film morphology and electrical conductivity measurements show that the layers attain a light-to-dark photosensitivity ratio of 2 × 10³ making them suitable for application in optoelectronic devices.     

爆炸载荷作用下具有可折叠芯层夹芯梁的动态响应

基于目前研究最广泛的刚性折纸(Tachi-origami)样式,通过改变其初始折叠角度构建出4种不同的蜂窝胞元,并且通过排列分布将其组成夹芯梁。采用商用有限元软件Abaqus/explicit对准静态和爆炸载荷作用下可折叠芯层夹芯梁的力学响应进行研究,分析可折叠芯层的泊松比变化规律、夹芯梁背板挠度以及能量吸收机理;并将夹芯梁与等质量的实体梁进行对比。采用后面板最大挠度作为抗爆性能的评价,结果发现:可折叠芯层在准静态载荷下具有一定的负泊松比效应;夹芯梁的抗爆性能优于实体梁,曲边蜂窝的初始折角对其作为芯层夹芯梁的抗爆性能有较大影响,随着初始折角的逐渐增大,其抗爆性能逐渐下降;当初始折角为直角时对应于方孔直边蜂窝,其抗爆性能最差。     

B炸药慢速烤燃过程的流变特性

为进一步探究熔铸炸药在烤燃过程中内部各物理场的变化情况,以B炸药为研究对象,完整地建立了基于Bingham流体模型的B炸药黏度计算模型并应用于慢速烤燃的数值模拟。通过数值模拟得到了B炸药在整个升温过程中上中下3个内部测点处的温度变化曲线并以烤燃试验加以验证,观察了弹体内部温度场与对流场的变化特点。结果表明:升温速率为1℃/min时,B炸药相变后逐渐开始流动,内部的温度场分布也随之改变,炸药出现自热反应与最终响应的区域都在弹体上部;升温速率为0.055℃/min时,炸药相变后内部很长时间内仍表现出类固相温度场的分布特点,当炸药出现自热反应后,才逐渐开始流动,温度场也逐渐转变为典型的液相温度场,炸药最终响应点在弹体上部,但最早出现自热反应的区域在弹体中心。     

MDYB-3有机玻璃在不同应变率下的一维屈服行为

对MDYB-3有机玻璃进行了多组不同应变率(10-3~3 000 s-1)下的压缩实验, 得到准静态下的屈服应力与动态下的峰值应力。沿其增强与面内2个方向进行准静态压缩实验, 以分析定向拉伸对屈服应力的影响, 修正了Ree-Eyring模型与Cooperative模型以描述定向有机玻璃的屈服行为。采用Johnson-Cook模型描述屈服后的黏塑性行为。结果表明Cooperative屈服模型比Ree-Eyring屈服模型更接近实验结果, 且能准确描述准静态屈服应力。动态压缩下的峰值应力为失效应力, 说明试样在1 500 s-1以上应变率下未达到屈服应力时已经发生破坏。Johnson-Cook模型对于单条曲线拟合良好, 但无法准确描述材料的应变率相关性。