电热原子吸收光谱法中原子化过程动力学研究的最新进展

本文评述了1994－2000年年间电热原子吸收光谱法中原子化过程动力学研究的最新进展,内容包括升温原子化过程动力学参数测定方法、等温原子化过程动力学参数测定方法、动力学参数测定方法的比较、双先导物升温原子化过程的动力学模型、考虑原子蒸气再沉积过程的升温原子化过程的动力学模型以及原子化器表面、基体改进剂及干扰物对分析物原子化过程的影响。引用文献31篇。     

激光扫描技术在靶场测试中的应用研究

为了解决光电类仪器在武器射击准确度和射击密集度的测试中遇到天空背景亮度不够,或弹丸口径小,弹道偏高而无法测试的问题,利用旋转棱镜使激光束在空中扫描,照亮弹丸表面,从而大大降低对光电传感器灵敏度的要求,使得该项测试工作不受天空背景条件的影响,并提高测试精度.     

Femtosecond laser ablation of Au film around single pulse threshold

Ablation process of 1-kHz femtosecond lasers (pulse duration of 148 fs, wavelength of 775 nm) of Au film on silica substrates is studied. The thresholds for single and multi pulses can be obtained directly from the relation between the squared diameter D2 of the ablated craters and the laser fluence φo. From the plot of the accumulated laser fluence Nφth(N) and the number of laser pulses N, incubation coefficient of Au film is obtained to be 0.765. Some experimental data obtained around the single pulse threshold are in good agreement with the theoretical calculation.     

Room temperature continuous wave operation of 1.33-μm InAs/GaAs quantum dot laser with high output power

Continuous wave operation of a semiconductor laser diode based on five stacks of InAs quantum dots (QDs) embedded within strained InGaAs quantum wells as an active region is demonstrated. At room temperature, 355-Mw output power at ground state of 1.33-1.35μm for a 20-μm ridge-waveguide laser without facet coating is achieved. By optimizing the molecular beam epitaxy (MBE) growth conditions,the QD density per layer is raised to 4 × 1010 cm-2. The laser keeps lasing at ground state until the temperature reaches 65 ℃.     

Luminescent Properties of a Polymer Photoluminescent Composite Containing the Binuclear (EU,TB) Complex as an Emitter

Uninuclear europium (Eu), as well as binuclear Eu and terbium (Tb), complexes were synthesized using acrylic acid (AA) as the first ligand and 1,10-phenanthroline (Phen) as the second ligand. The relative weight ratio of the europium (III) (Eu³⁺) to terbium (III) (Tb³⁺) ions of the binuclear complex was 1:1 as determined via energy dispersive X-ray analysis. The structures of the Eu(AA)₃Phen and Eu_0.5Tb_0.5(AA)₃Phen complexes were characterized by Fourier transform infrared spectroscopy. A series of tri-cellulose acetate (TCA)/ the Eu(AA)₃Phen and TCA/Eu_0.5Tb_0.5(AA)₃Phen composites were prepared by solution blending, and their luminescent properties were investigated by fluorescence spectrophotometry. The excitation spectra of all composites indicated that the TCA matrix probably affected the energy absorption and transfer of organic ligands. In TCA/Eu_0.5Tb_0.5(AA)₃Phen composites the introduced Tb³⁺ ions had some influence on energy absorption and transfer of organic ligands; the energy transfer process of the complex is suggested to be as follows: Phen→AA→Tb³⁺ion→Eu³⁺ion. The emission spectra indicated that the luminescent intensity of the TCA/Eu_0.5Tb_0.5(AA)₃Phen composites was noticeably stronger than that of the TCA/Eu(AA)₃Phen composites, suggesting that the comparatively stable and high-efficiency energy transfer process was only slightly influenced by the TCA matrix. In summary, the TCA/Eu_0.5Tb_0.5(AA)₃Phen (90/10) composite possesses fine luminescent properties for potential usage as red fluorescent materials.     

Deterministic Bidirectional Remote State Preparation of a- and Symmetric Quantum States with a Proper Quantum Channel

We present a new scheme for deterministically realizing the mutual interchange of quantum information between two distant parties via selected quantum states as the shared entangled resource. We first show the symmetric bidirectional remote state preparation (BRSP), where two single-qubit quantum states will be simultaneously exchanged in a deterministic manner provided that each of the users performs single-qubit von Neumann measurements with proper measurement bases as well as appropriate unitary operations, depending essentially on the outcomes of the prior measurements. Then we consider to extend the symmetric protocol to an asymmetric case, in which BRSP of a general single-qubit state and an arbitrary two-qubit state is investigated successfully. The necessary quantum operations and the employed quantum resources are feasible according to the present technology, resulting in that this protocol may be realizable in the realm of current physical experiment.     

First-principles investigation on ideal strength of B2 NiAl and NiTi alloys

For B2 NiAl and NiTi intermetallic compounds, the ideal stress–strain image is lack from the perspective of elastic constants. We use first-principles calculation to investigate the ideal strength and elastic behavior under the tensile and shear loads. The relation between the ideal strength and elastic constants is found. The uniaxial tension of NiAl and NiTi along <001> crystal direction leads to the change from tetragonal path to orthogonal path, which is driven by the vanishing of the shear constant C(66). The shear failure under {110}{111} shear deformation occurring in process of tension may result in a small ideal tensile strength(~ 2 GPa) for NiTi. The unlikeness in the ideal strength of Ni Al and Ni Ti alloys is discussed based on the charge density difference.     

Luminescence behavior of Tb ions in transparent glass and glass-ceramics containing CaF2 nanocrystals

Transparent glass-ceramics have been fabricated by heat treatment with 1.0 mol% Tb₂O₃-doped 45SiO₂-20Al₂O₃-10CaO-25CaF₂ aluminosilicate glass. The precipitated crystalline phase in the glass-ceramics is CaF₂ nanocrystals with a size of 15-27 nm and dispersed in the amorphous phase. Both photo- and radioluminescence measurements show that the increase of Tb³⁺ 545 nm line intensity by a factor of 4 and 3.5 is obtained in glass-ceramics with respect to the as-made glass, respectively.     

磁性功能化酚醛树脂的合成及对金属离子的吸附性能

磁性功能化酚醛树脂的合成及对金属离子的吸附性能;环氧酚醛树脂;螯合;金属离子;溶胀;吸附容量;吸附动力学     

由NO分子从头计算结果和紫外光电子能谱确定NO的分子结构

对于NO分子轨道的能级次序现有两种不同的说法,不少人根据NO与O_2~+是等电子体,由O_2~+分子的能级次序确定NO分子组态。本文用NO和O_2~(+)从头计算结果以及NO的紫外光电子能谱相结合的方法说明NO的5σ轨道是弱成键轨道,5σ的轨道能稍高于1π轨道能,也就是说NO的能级次序是与N_2分子相同的;NO与O_2~+虽是等电子体,但是能级次序并不相同,因此由O_2~+的能级次序确定NO分子的电子组态是不妥的。