石英砂在菱苦土磨具中的作用机理

本文利用物质结构与化学键的有关理论对石英砂的菱苦土磨具中的作用机理进行分析，并以实验对分析结果进行验证。结果表明：金刚砂晶体中Si-C共价键的离子性百分数仅为9％，石英晶体中Si-O共价键的离子性百分数为47％，因此，石英与主要以离子键结合的菱苦土结合剂之间有较强的静电作用力，石英与菱苦土的结合力强于金刚砂，可提高菱苦土磨具的耐磨性。     

Investigations of ultrathin polypyrrole films: Formation and effects of doping/dedoping processes on its optical properties by electrochemical surface plasmon resonance (ESPR)

In the present work an investigation of the effects of the electropolymerization mode on the optical properties associated to the doping/dedoping processes of nanometric films of polypyrrole (PPy) is reported, monitoring in situ and in real time using simultaneously surface plasmon resonance and electrochemical techniques (ESPR). The electropolymerization of pyrrole was performed by potentiostatic, potentiodynamic and galvanostatic methods and the use of the ESPR technique showed that the electropolymerization mode is essential to the stability of polymer and the reversibility of its optical properties during the doping and dedoping processes. Thus, the optical properties of oxidized and reduced film were obtained by nonlinear least square fitting using Fresnel equations for a four-layer system. Then, the values of the real and imaginary parts of the complex dielectric constant for PPy fims were correlated with the polymer doping level. Finally, quartz crystal microbalance measurements were also applied to obtain correlation between doping/dedoping processes and the changes in the real and imaginary parts of the dielectric constant of the polypyrrole film, showing that the doping and dedoping processes in the polypyrrole film can act directly on its optical properties while the ESPR technique can give the same information indirectly.     

单色光石英退偏器的退偏机理及性能研究

研究了单色光石英退偏器的退偏机理；定义了退偏度作为衡量退偏器性能的物理量。从实验上在４４０～９２０ｎｍ的光谱范围测试了器件的退偏度，结果表明：只要器件的结构角适当，或者适当调节入射光束的截面大小，便可对某一单色线偏振光实现很好的退偏。     

冻融循环下云母石英片岩三轴力学特性与强度预测模型

为探究云母石英片岩物理力学特性受冻融循环作用的影响,对饱水云母石英片岩开展了0、25、50、75、100次冻融循环试验,并对试样分别进行了4级围压下的常规三轴压缩试验,研究了其动弹性参数、三轴压缩破坏形式及三轴抗压强度的变化规律,取得如下成果:①随着冻融循环次数的增加,三轴抗压强度、动弹性模量、动剪切模量及动体积模量呈指数衰减,黏聚力及内摩擦角则呈线性衰减趋势;②随着冻融循环的进行,围压对试样强度的增大作用逐渐削弱,冻融循环对试样强度的劣化作用逐渐凸显;③冻融作用使云母石英片岩三轴压缩破坏形态由张拉破坏逐步演化为顺片理剪切破坏;④基于Jaeger破坏准则建立了一种以冻融循环次数、片理面倾角及围压为控制参数的斜交片理云母石英片岩三轴抗压强度预测模型,预测结果与实测数据具有较好的一致性。研究成果可为研究云母石英片岩冻融损伤劣化规律提供参考。     

石英晶体振荡器的微处理器温度补偿技术研究

为改善石英晶体振荡器的频率特性,减小温度影响,通过对石英晶体振荡器的频率-温度特性的研究,提出了以微处理器（STC89C52RC）为核心的基于AT切晶体谐振器的温度补偿技术,并介绍了系统结构、补偿原理及硬件电路,给出了补偿结果。本设计具有结构简单、功耗低等优点。     

小秦岭NNE向金矿脉构造变形特征与成矿关系

小秦岭金矿田位于华北克拉通南缘的华熊地块北缘,发育有产出于不同走向剪切带内的金矿脉。但是,目前研究和认识对矿脉和剪切带、以及不同方向矿脉之间的构造关系并不清晰。选择小秦岭中部善车峪一带的典型NNE向矿脉开展构造变形与矿化特征研究。结果表明:NNE向金矿脉以右阶排列的石英脉透镜体为特征,主体产状为120°∠70°; 矿脉产出于与之近平行的左行逆冲剪切带内,并改造了早期近EW向剪切带,其所处构造应力场环境为近EW向水平伸展; 矿体的主要矿石矿物为方铅矿、黄铁矿、闪锌矿等多金属硫化物,这些金属矿物多呈条带状或条纹状沿剪切面理或小角度斜交的张剪性面理贯入,显示与左行逆冲变形同期形成的特征。构造变形序列和矿化特征对比分析显示,小秦岭地区NNE向矿脉叠加改造了近EW向矿脉,其构造应力场环境分别与早白垩世和晚三叠世区域应力场特征一致。前人对于岩浆作用、成矿流体和成矿时代等方面的研究结果认为,小秦岭地区经历了印支期和燕山期两期构造与成矿作用的叠加,从而推测NNE向金矿脉应形成于燕山期陆内构造变形阶段,而近EW向矿脉可能形成于印支期华北板块和扬子板块碰撞拼贴阶段。     

Passivation of Fe-Cr alloys studied with ICP-AES and EQCM

The response of sputter deposited Fe-15Cr and Fe-25Cr alloys to a rapid potential increase in the passive region was studied using two in situ methods: electrochemical quartz crystal microbalance and inductive coupled plasma-atomic emission spectroscopy (ICP-AES). Both methods indicated an increase in the dissolution rate of iron following the potential change; the total amount of material dissolved being higher for the Fe-15Cr alloy. For both alloys, about 10% of the total dissolved material was Cr. This result compared well with experiments on a 430 stainless steel. ICP-AES is shown to be useful for the in situ determination of partial currents of metal dissolution using solution analysis in a flow cell.     

高聚物湿度传感器的研究

本文介绍采用辐射引发聚合的方法制备高聚物/晶振型湿度传感器。通过对高聚物膜的感湿性能测试与评价,确定聚合物膜中各单体组分含量,并优化辐射聚合工艺。该高聚物/晶振型湿度传感器的技术特点是:湿度测量范围宽10％～100％RH;湿滞回差小,测量误差小于±2％RH。尤其适于在易燃易爆环境下应用。     

石英晶体微天平的研究进展综述

石英晶体微天平(QCM)能够感知到纳克级的质量变化,在分析化学、电化学、有机化学、生物医学等方面得到了广泛的应用。根据与QCM电极表面相接触的研究介质即应用对象的不同,分别阐述了刚性薄层、牛顿流体、粘弹性膜层的基础方程、分析方法及应用,并探讨了其存在的问题与发展趋势。     

Electrodeposition and dissolution of yttrium-hexacyanoferrate layers

The electrodeposition and dissolution of yttrium-hexacyanoferrate [YHCNFe(II)] were investigated by electrochemical quartz crystal microbalance technique (EQCM). The electrodeposition was carried out by potential cycling or stepping from solutions of Y(NO₃)₃ and K₃[Fe^III(CN)₆] of different concentrations. The ratio of the reactants was also varied. No deposition was found in dilute solutions (c < 10⁻³ mol dm⁻³). The increase of concentrations led to an intense deposition of YHCNFe(II) in the course of reduction of [Fe^III(CN)₆]³⁻. At high concentrations of the reactants a coagulation deposition of YHCNFe(III) at open-circuit has also been detected. During the reduction the first phase is the nucleation which requires saturation or oversaturation in respect to the reacting species near the gold surface. The growth phase is much faster than the formation of nuclei, and its rate depends on the concentration and the concentration ratio of the species. The composition of the deposits has been determined by total reflection X-ray fluorescence (TXRF) spectrometry. From the molar ratio of atomic constituents (K, Y and Fe) of the slightly soluble deposit (solubility: 5 × 10⁻⁵ mol dm⁻³) formed after reduction of Fe(III) a formula K_0.46Y_1.18[Fe^II(CN)₆] can be derived. This value is in good accordance with the molar mass calculated from the results of EQCM experiments which also revealed that the deposit contains ca. 2 mol H₂O/mol YHCNFe(II). The solubility of YHCNFe(III) is substantially higher (s = 2 × 10⁻³ mol dm⁻³), and according to the results of TXRF measurements, its composition is Y[Fe^III(CN)₆]. The reoxidation of YHCNFe(II) takes place in two steps. The first one is a partial oxidation which is accompanied by the desorption of K⁺ ions from the layer. During further oxidation a fast dissolution occurs due to the high solubility of YHCNFe(III).