运用液体声学理论研究超临界二氧化碳的声特性

利用液体声学模型，根据美国国家标准局提供的二氧化碳声速、密度、摩尔体积和绝热压缩系数数据，计算了气态、液态和超临界态二氧化碳在不同温度和压力条件下的摩尔声速、摩尔压缩系数及Van der Waals 常数. 分析发现，在较宽的温度和压力范围内，液体中的声学模型能够很好地运用于超临界态二氧化碳的研究. 并在液体声学模型适用范围内，计算了超临界二氧化碳在不同温度及压力状态下的表面张力、粘度、自扩散系数，为超临界流体技术提供了参考数据，并分析了这些参量的变化规律.     

超临界点附近二氧化碳流体的声速

使用压缩蒸气模型,推导了超临界流体在超临界点附近区间的声速表达式,表达式揭示了声速和密度波动指数、等温压缩系数、定体摩尔热容量等参量的联系.在超临界点附近,二氧化碳流体的声速和密度波动指数呈减函数关系,密度波动指数越大,声速越小,在密度波动指数最小处,声速最大,此时,较小的密度波动会引起较大的声速波动.当压强逐渐增大并接近临界点时,定体热摩尔容量的迅速增大导致声速减小,当压强增大而远离临界点时,定体摩尔热容量的迅速减小导致声速增大.由表达式得到的计算值与由美国国家标准局提供的参考值符合较好. 关键词： 超临界二氧化碳 声速 密度波动 定体摩尔热容量     

海底表层沉积物声速的环境因素影响特性

应用声速通用模型开展理论分析,结合温度-压力可控实验测量分析,研究地声反演、海底原位声学测量和采样样品声学测量3种主要的海底表层沉积物声学特性测量方法中,存在的环境因素影响机制和特性。理论计算与实验测量研究具有一致性,揭示温度和静水压力对海底表层沉积物的压缩波声速的影响机制主要是通过影响孔隙海水的密度、黏度、体积弹性模量体现的。在海底4000 m以内的表层海底沉积物通常存在的海底温度和静水压力范围内,发现声速比不为常数,随着温度升高和静水压力增大而呈现出细微减小趋势,理论计算海底沉积物与底层海水声速比波动度在2%以内,实验测量声速比波动度在2.73%以内。基于声速比不为常数,提出修正声速比校正模型,为减小温度和静水压力影响因素误差,更准确地实现不同原位、实验室环境状态下的海底沉积物声速的分析和比较提供了改进方法。      

多元有机混合液声速特性与非线性声参量B/A的数值计算

根据Jacobson的液体分子自由程理论和液体声速与分子自由程的关系,推导出多元有机混合液声速的温度系数、压力系数和非线性声参量B/A的计算公式,并根据组成多元有机混合液各组分特性参量(密度、自由程、非线性声参量B/A、等压膨胀系数、等温压缩系数等),利用给出的公式对声速的温度系数、压力系数、非线性声参量B/A进行了数值计算,并将计算结果与实验结果进行了比较.     

石油醚在流体静高压下的超声声速、衰减、密度和绝热压缩系数

 专门设计了用脉冲-回波-重合法在不同静水压下测量液体声速的装置，并对石油醚在0.1~650 MPa流体静压力范围内测量了其超声声速和衰减系数。还通过测量体积压缩量和质量得到石油醚密度ρ随流体静压力的变化。最后，给出了石油醚的绝热压缩系数β与流体静压力的关系。     

F113、CCI4及其混合液体的声速

从已得的F₁₁₃、CCl₄及其混合液体的声速经验公式,计算了F₁₁₃、CCl₄及其混合液体的声速.绘出了定混合比下的声速与温度的关系曲线和定温度下的声速与混合比的关系曲线.给使用这些声速者提供参考.     

过氧化氢水溶液的超声研究

本项研究用脉冲回波自动声速仪测量了过氧化氢水溶液的声速与温度，浓度关系，声速测量精度约０．５×１０＾－＾４。计算了溶液的摩尔声速，绝热压缩系数，声阻抗以及纯过氧化氢声速等参量，作者确信，这些参量属首次公开报道，文中还讨论了声学参量随溶液浓度的变化特性。研究结果妇现，声速值和除了绝热压缩系数以外的声学参量都随溶液浓度的增加而增加。     

小分子液体的高温布里渊散射研究

利用金刚石对顶砧技术,采用180°背向散射和60°前向对称散射两种几何配置,对水、氨、二水合氨和甲烷等含氢小分子液体进行了高温高压布里渊散射研究,计算了在室温(296K)和高温(410K)下的声速,比较了不同小分子液体中的声速及绝热体弹模量随压力的变化关系。在等温条件下,各体系中声速随着压力的增加逐渐增加;在相同温度下,甲烷液体的声速随着压力增加的速率明显高于水、氨及二水合氨液体;在相同的温度和压力条件下,水、氨及二水合氨液体的体弹模量明显高于甲烷液体的体弹模量,表明氢键的存在对于小分子液体弹性具有较大影响。二水合氨的体弹模量斜率在1.5GPa左右发生改变,表明液体结构可能发生了改变,并分析了氢键对该体系弹性性质的影响。研究有助于理解其他含氢小分子液体中压力和温度诱导的分子结构变化。     

超声波流量计测量流体声速的实验方法

为获取液体介质的声速值,设计了一种测定流体声速的实验方法,该方法利用时差式超声波流量计和标准流量校验设备同时对封闭管道中的液体进行流速测量,分别得到流速的测量值和真实值,从而计算出超声波流量计的仪表系数,并以此导出了一定条件下液体介质的声速值随仪表系数的变化关系式.利用该方法测量给出了0.17 MPa下四氧化二氮(N₂O₄)在7.6-19.4 ℃、偏二甲肼((CH₃)₂NNH₂)在6.5-25.2 ℃范围内的流体声速值,并为其他液体介质的声速测量提供了借鉴. 关键词： 超声波流量计 声速 仪表系数 温度     

高压下Fe3C的磁性和声速性质

采用基于密度泛函理论的包含自旋极化效应的广义梯度近似方法研究了Fe₃C的高压弹性和声学性质. Fe₃C在压力作用下由铁磁基态转变到非磁性的高压态,相变压力约为73 GPa. 计算了Fe₃C 的Hugoniot线,并根据沿Hugoniot线的弹性常数计算了铁磁状态和非磁性状态的声速. 对比Fe单质,非磁性Fe₃C 的压缩波和剪切波声速与地核的地震波数据更为接近,证实了C元素是构成地核的一种成分.     

Ultrasonic study of nitric acid

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Ultrasonic and IR study of intermolecular association through hydrogen bonding in ternary liquid mixtures

Complex formation in ternary liquid mixtures of dimethylsulfoxide (DMSO) with phenol and o-cresol in carbontetrachloride has been studied by measuring ultrasonic velocity at 2 MHz, in the concentration range of 0.019-0.162 (in mole fraction of DMSO) at varying temperatures of 20, 30 and 40 degrees C. Using measured values of ultrasonic velocity, other parameters such as adiabatic compressibility, intermolecular free length, molar sound velocity, molar compressibility, specific acoustic impedance and molar volume have been evaluated. These parameters have been utilized to study the solute-solute interactions in these systems. The ultrasonic velocity shows a maxima and adiabatic compressibility a corresponding minima as a function of concentration for these mixtures. The results indicate the occurrence of complex formation between unlike molecules through intermolecular hydrogen bonding between oxygen atom of DMSO molecule and hydrogen atom of phenol and o-cresol molecules. The excess values of adiabatic compressibility and intermolecular free length have also been evaluated. The variation of both these parameters with concentration also indicates the possibility of the complex formation in these systems. Further, to investigate the presence of O-HO bond complexes and the strength of molecular association with concentrations, the infrared spectra of both the systems, DMSO-phenol and DMSO-o-cresol, have been recorded for various concentrations at room temperature (20 degrees C). The results obtained using infrared spectroscopy for both the systems also support the occurrence of complex formation through intermolecular hydrogen bonding in these ternary liquid mixtures.     

Estimating organic chain length through sound velocity measurements

The ability to measure the length of polymers while monitoring their production is evidently extremely valuable, but is also a useful tool for chemical identification purposes at other times, e.g. the analysis of waste water. A study of the relationship between velocity of sound and chain length has been carried out. Initial studies were performed on two model systems; a series of pure liquid n-alkanes (pentane to hexadecane) and 1-alcohols (methanol to 1-dodecanol). This study was extended to look at an industrially significant system of dimethylsiloxanes 200 fluid (L2, 0.65 cSt) to 200 fluid (5000 cSt). Corresponding density data have been taken from the literature and the adiabatic compressibility determined. The measured adiabatic compressibility has been compared with two molecular models of wound velocity, the Schaaffs model and a development of the Urick equation. The Urick equation approach is based on a determination of the compressibility of the methylene or siloxane repeat units which make up the chains in these linear molecules. We show that the Urick equation approach accurately predicts sound velocity and compressibility for the higher members of each series, whilst the Schaaffs approach fails for the 1-alcohols. We suggest that this is because of the influence of the hydroxyl end group through hydrogen bonding with methylene groups within the chain. This interaction modifies the derived compressibility of the methylene groups, so reducing their compressibility relative to that of the n-alkanes. The technique described provides valuable new insights into end-group, intermolecular and intra-molecular interactions in liquid linear-chain molecules. From this detailed analysis of the mechanisms involved, a model is derived. This model can give very precise estimations of the composition of a pure liquid. In the case of mixtures of polymers, it is necessary to use the modified Urick equation and then, in addition, the concentration dependence of both the velocity of sound and the density must be measured.     

The fast-ion transition in FCC silver iodide

An analysis of previously reported data on electrical conductivity, adiabatic temperature change with pressure, and sound velocity confirms that the FCC phase of AgI has a fast-ion type II transition. This results in a steepening of the FCC/α-phase boundary which probably cusps in to a triple point at the α-phase order/disorder transition. Thermal expansion, compressibility and heat capacity are calculated for the FCC phase.     

Specification of the acoustical input to the ear at high frequencies

The sound fields that arise in the auditory canals of cats have been examined both experimentally and theoretically. Of particular interest was the spatial variation of sound pressure near the eardrum, where reference probes are typically located. Using a computer controlled data acquisition system, sound pressure was measured between 100 Hz and 33 kHz for constant driver input at 14 different locations in the ear canal of a cat, and the standing wave patterns formed. The shape of the patterns could be predicted quite well above 12 kHz using a theory that requires specification of only the geometry of the ear canal. This theory, an extension of the one-dimensional horn equation, applies to three-dimensional, rigid-walled tubes that have both variable cross section and curvature along their lengths. Large variations of sound pressure along the ear canal and over the surface of the eardrum are found above about 10 kHz. As a consequence it is not possible to define the acoustical input to the ear from sound pressure level measured at any single location. Even in comparative experiments, in which only the constancy of the acoustical input is important, any uncertainty in reference probe location would lead to an uncertainty in sound pressure level when different sets of measurements are compared. This error, calculated for various probe locations and frequencies, is especially large when the probe is near a minimum of the sound field. Spatial variations in pressure can also introduce anomalous features into the measured frequency response of other auditory quantities when eardrum sound pressure is used as a reference. This is illustrated with measurements of the round window cochlear microphonic.     

Phase transition studies in N(p-n-pentyloxy benzylidene) p-n-decyl aniline

The temperature dependences of the molar volume, the ultrasonic velocity and the refractive index in N(p-n-pentyloxy benzylidene) p-n-decyl aniline, which exhibits nematic, smectic-A and smectic-B, phases, are presented. The isotropic-nematic and smectic-A-smectic-B phase transitions are found to be of first order while the nematic-smectic-A transition is of second order. The thermal expansion coefficient (a) computed from the molar volume data agrees with a second-order N-S_A transition. The computed adiabatic compressibility β_ad, molar sound velocity (or Rao number R_n ) and molar compressibility (or Wada constant A) are presented.     

Phase diagram involving the mesomorphic behavior of binary mixture of sodium oleate and orthophosphoric acid

The present investigation deals with the binary mixture of two non-mesogenic compounds, viz. sodium oleate (Naol) and orthophosphoric acid (H₃PO₄) which exhibits very interesting liquid crystalline smectic phases at large range of concentrations and temperature. The mixtures with concentrations ranging from 10% to 90% Naol in H₃PO₄ exhibit SmA, SmC, SmE and SmB phases, sequentially when the specimen is cooled from its isotropic phase. Physical properties, such as ultrasonic velocity, adiabatic compressibility and molar compressibility, show anomalous behavior at the isotropic to mesosphase transition.     

Phase transition studies in N-(p-n-pentyloxy benzylidene) p-Toluidine

The variations of molar volume M_v and ultrasonic velocity V with temperature in N(p-n-pentyloxy benzylidene) p-toluidine are presented. The molar volume jump at the nematicisotropic transition suggests it is of first order. The adiabatic compressibility β _ad, molar sound velocity or Rao number R_n , molar compressibility or Wada constant A, the thermal expansion coefficient α, and Van der Waals constant b, are computed. Molar sound velocity and molar compressibility are compared with the values of other members of the homologous series and are found to be in good agreement with Rao's and Wada's observations. The order parameter S_k, at the nematic-isotropic phase transition is 0.441 from our experimental results and the Maier-Saupe table and is found to be in good agreement with the theoretical value.     

Density, viscosity and ultrasonic velocity studies of aqueous solutions of sodium acetate at different temperatures

The densities and viscosities of aqueous solutions of sodium acetate have been measured at 298.15, 303.15, 308.15 and 313.15 K and at atmospheric pressure. The molality range has been studied between 6.09 × 10^− 2 to 7.314 × 10^− 1 mol kg^− 1. The experimental values of density have been used to calculate apparent molar volume, partial molar volume, solute–solute interaction parameter, and Hepler's constant. The viscosity data have been analyzed with Jone–Dole equation. Furthermore, ultrasonic velocity measurements of aqueous solutions of sodium acetate have been made at 298.15 and 308.15 K and at atmospheric pressure. From experimental values of ultrasonic velocity, apparent molar isentropic compressibility and limiting apparent molar isentropic compressibility have been calculated. All the parameters calculated from density, viscosity, and ultrasonic velocity indicate that the sodium acetate is water structure maker.