氧碘化学激光中的增益光导效应

发现和分析了氧碘化学激光中的增益光导效应。碘注入的不均匀等导致增益在该方向的不均匀。采用预混模型和Fabry Perot腔模型,推导了碘不均匀分布情况下的单重态氧的产额和激光束横向分布的解析表达式。计算结果表明,由于增益光导效应,引起激光横向分布的变化,可导致光束在碘注入方向的倾斜,以及输出功率的下降。     

采用介质偏移技术的LTE基站双工器

为了在小尺寸且较低加工难度的情况下实现模式可控的多模双工器,一种新型双工器设计法——介质偏移技术被提出。根据对介质偏移多模谐振器谐振特性的分析,建立耦合矩阵,通过耦合系数与物理参数的关系算出理论物理参数值,最后通过仿真软件优化各个物理参数值。利用该技术设计了两个具有尺寸小、插损低和功率容量高等优点的长期演进(LTE)基站的双工器,丰富和发展了基站双工器的设计方法。     

Anchoring of hydrophobically modified poly(sodium acrylate)s into DDP vesicle bilayers: hydrophobic match and mismatch

 Differential scanning microcalorimetric thermograms have been recorded for aqueous solutions containing vesicles formed by sodium di-n-dodecyl phosphate, in the presence of different concentrations of poly(sodium acrylate-co-n-alkyl methacrylate), where n-alkyl= C₉H₁₉, C₁₂H₂₅, C₁₈H₃₇. The mole fraction of hydrophobic moieties in the copolymer is 0.04. The main phase transition temperature (T _m) is hardly affected by the presence of poly(sodium acrylate)s bearing n-dodecyl chains, whereas the anchoring of polymers bearing n-nonyl or n-octadecyl groups reduces the main phase transition temperature significantly from ca. 34 °C to ca. 32 °C. In parallel, the enthalpy of transition per mole of DDP monomer (Δ_m H _int) is lowered upon adding polymer. Again, the polymer containing n-dodecyl moieties hardly affects Δ_m H _int. These patterns are explained by the notion that the extent of the disruptive effect of alkyl chains incorporated into the bilayer depends on the extent of the mismatch between the chain lengths of the intruding alkyl chains and the hydrophobic moieties composing the vesicle bilayer. Added hydrophobically modified polymers increase the cooperativity of the melting process, as shown by the increase of n _DDP. We suggest that the anchoring poly(sodium acrylate-co-n-alkyl methacrylate) relieves the strain in the curved outer monolayer of a pure DDP bilayer by allowing the presence of larger “patches” characterized by low curvature. Received: 12 May 1997 Accepted: 20 October 1997     

回传信号传输受阻现象的分析及对策

针对维修中遇到的上网回传信号传输受阻现象,通过对线路的接头部位与线缆部位出现的氧化现象进行分析,找出了故障产生的原因,并通过维修案例验证了分析的正确性,进一步提出了规范施工对网络稳定运行的重要性。     

循环前缀中插入四元序列的频偏估计研究

研究了一种在循环前缀中插入四元序列的载波频偏估计方法。由于在循环前缀中添加的四元序列自身携带的相位信息丰富,因此可以利用其这一特点完成对载波频偏的估计。该方法实现简单,且不限制特定的调制方式,在基于循环前缀的OFDM系统上稍加改进即可实现本系统的设计,降低了系统实现的复杂度。通过仿真表明在信噪比大于16 dB并且序列长度较短时,所提算法即可以满足系统对载波频偏估计的要求。     

介电失配度对沸石电流变液界面极化的影响

利用介电谱方法研究了NaA沸石/硅油和NaA沸石/煤油两种电流变液的介电行为, 测量发现两体系在10⁵ Hz处均出现明显的弛豫现象. 采用单弛豫Cole-Cole函数拟合各体系的介电参数, 结果表明在相同体积分数条件下硅油体系具有较大的介电增量(?ε), 且两体系的介电增量与体积分数(φ)均服从?ε＝4ε_mφ的函数关系. 通过计算和分析粒子与介质间介电失配程度, 阐明了油介质的介电常数(ε_m)对于沸石电流变液界面极化强度的贡献. 此外研究了吸附水对沸石电流变液界面极化的影响, 结果发现水的吸附对于体系的?ε值没有影响, 但明显降低了弛豫时间, 证明吸附水对沸石电流变液的界面极化率具有增强作用.     

Sensing method based on impedance variation of minicolumn packed with cation-exchanger under electric field

Voltage-induced impedance variation of the minicolumn (i.d. 0.53 mm, length 2 mm) packed with cation exchanger was investigated to develop a sensing method. An aqueous sample solution containing the metal cations was continuously supplied to the minicolumn during the impedance measurement with the simultaneous application of both alternating current voltage (amplitude, 1.0 V; frequency, 200 kHz to 6 Hz) and direct current (DC) offset voltage (0.1 to 1.0 V). On a complex plane plot, the profile of the column impedance consisted of a semicircle (200 kHz to 100 Hz) and a straight line (<100 Hz), of which slope varied with the magnitude of the applied DC offset voltage (V _DC). The slope–V _DC relation depended on the kind of the metal cation and its concentration; in particular, the slope–V _DC relations of monovalent cations (Na⁺ and K⁺) and divalent ones (Mg²⁺ and Ca²⁺) were significantly different. With the change in the concentration of minor divalent salt of MgCl₂ or CaCl₂ (60 to 140 μM) in the sample solution containing 10 mM NaCl, the slopes showed almost linear relationships between those with application of V _DC = 0.1 V and 1.0 V both for magnesium and calcium additions. In the case of plural addition of both MgCl₂ and CaCl₂ to the solution, the data points in the slope_{0.1  V}–slope_{1.0  V} plot were located between the two proportional lines for single additions of magnesium and calcium, reflecting both the mixing ratio and net concentrations of the divalent cations. Thus, simulations determination of Mg²⁺ and Ca²⁺ can be attained on the basis of the slope_{0.1  V}–slope_{1.0  V} relation obtained by the impedance measurements of the minicolumn. Actually, the contents of both magnesium and calcium cations in the bottled mineral waters determined simultaneously using the proposed method were almost equivalent to those obtained by the atomic absorption spectrometric measurement.     

Nanoscale three‐dimensional optical visualization method for a deformation of elastomer printing plate to realize soft nano‐printing technology

Printed electronics, in which microcircuit patterns are fabricated using printing methods, are the focus of considerable attention for the fabrication of devices such as flat panel displays, solar cells, and flexible electronics. In particular, gravure offset printing is considered to be a highly promising approach for rapid printing of fine patterns with well‐controlled thickness. At present, however, because of the occurrence of side etching during fabrication of metal printing plates, features with dimensions of less than 10 µm cannot be printed. In order to overcome this problem, we have previously proposed the use of a rubber printing plate fabricated by photolithography and molding, which is free from side‐etching issues. However, deformation of the printing plate can have a detrimental influence on the transferred pattern. In the present study, we developed a method for visualizing the deformation of a printing plate containing both micropatterns and nanopatterns, in order to study its effect on the printing process. The results were compared with those predicted by an analytic equation under a uniform controlled pressure. Copyright © 2015 John Wiley & Sons, Ltd.     

Paper-based solid-state electrochemiluminescence sensor using poly(sodium 4-styrenesulfonate) functionalized graphene/nafion composite film

Herein, highly efficient solid-state ECL sensor was introduced for the first time onto the screen printed electrodes of the paper-based chips (PCs) based on the composite film of poly(sodium 4-styrenesulfonate) functionalized graphene (PSSG) and Nafion. Attributed to the cooperative characteristics of both PSS and graphene, PSSG ensured both effective Ru(bpy)₃²⁺ immobilization and fast electron transfer of Ru(bpy)₃²⁺ in the composite film. The ECL behaviors at the developed sensor were investigated using tripropylamine as a representative analyte and low detection limit (S N⁻¹ = 3) of 5.0 nM was obtained. It also exhibited more excellent reproducibility (relative standard deviations of 0.63% for continuous 45 cycles) and long-term stability (∼80% of its initial ECL intensity could be retained over 3 months). More importantly, assisted by the developed ECL sensor, discrimination of 1.0 nM single-nucleotide mismatch in human urine matrix could be realized on the PCs for the first attempt. Thus, the developed sensor was confirmed with the advantages of highly sensitivity, long-term stability, simplicity, low cost, disposability, high efficiency and potential applicability.     

Electrophoretic mobility of duplex DNA cross‐linked by mechlorethamine at a cytosine–cytosine mismatch pair

The common nitrogen mustard, mechlorethamine, can form a covalent cross‐link between the two bases of a cytosine–cytosine mismatch pair within a DNA duplex. The cross‐linked species can be readily separated from DNA monoadducts and unreacted strands using denaturing polyacrylamide gel electrophoresis. Here, using DNA 19 mer duplexes that are mechlorethamine cross‐linked at a C₄–C₃₅, C₇–C₃₂, C₁₀–C₂₉, or C₁₃–C₂₆ mismatch pair, we show that the denaturing polyacrylamide gel electrophoresis mobility of the cross‐linked species is particularly sensitive to the proximity of the C–C cross‐link to the duplex end. Species that are cross‐linked at a C₄–C₃₅ mismatch have greater mobilities than those cross‐linked at C₇–C₃₂ or C₁₃–C₂₆, and the species with a central C₁₀–C₂₉ cross‐link have the lowest mobility. The mobility is also dependent on the proximity of the cross‐link to a 5′‐³²P‐phosphate or a 5′‐fluorescein label. We interpret these results in terms of the conformational properties of the cross‐linked species in the denaturing gel. The results are consistent with the retention of partial duplex character at the end proximal to the cross‐link, with an influence on the mobility of the GC/AT ratio proximal to the cross‐link and at the duplex end, and a small but discernible effect of the label.