Frequency dependence of acoustic properties of aqueous glucose solutions in the VHF/UHF range

The bioultrasonic spectroscopy system was employed for measurements of velocity and attenuation coefficient of glucose solutions in the VHF/UHF range. The relation between the slope of the square of velocity and the relaxation parameters, and the relation between the frequency exponent on attenuation coefficient and the relaxation parameters are investigated. In order to carry out numerical calculations, a model for a single relaxation process is employed, wherein the attenuation coefficient is expressed as (A/( 1 + (f/falpha)2) + B)f2 where falpha is the attenuation relaxation frequency, and A and B are constants. The numerical calculations show that the slope of the square of the velocity is determined uniquely by the velocity relaxation frequency fv and v(infinity)2 - v(0)2 where v0 is the zero-frequency velocity and v(infinity) is the infinite-frequency velocity, and that the frequency exponent on the attenuation coefficient is determined uniquely by falpha and A/B. For experimental considerations, the velocities and the attenuation coefficients of 5, 15, and 25% concentration aqueous solutions of glucose were measured in the frequency range 20 to 700 MHz. The data for the 5 and 15% aqueous solutions can be explained using the single relaxation model. However, the data for the 25% aqueous solution suggest the existence of multirelaxation processes.     

High-frequency attenuation measurements using an acoustic microscope

An acoustic microscope was used to measure excess attenuation of aqueous solutions of sugars and proteins at 1.0 GHz. Interference pattern spacing and peak amplitude reduction of V(z) curves, obtained with these solutions as the acoustic microscope coupling liquid, were related to the solution wavespeed and attenuation, respectively. Consistent with published results for lower frequencies, solutions with molecular weight greater than 10,000 had a higher specific absorption than those with a molecular weight less than 1000 and within these two molecular weight ranges specific absorption was independent of concentration.     

Biomolecular absorption of ultrasound. I: Molecular weight

Amino acid solutions have absorptions which are generally small compared to those for proteins. Proteolytic enzyme treatment of proteins in solution reduces their absorption. These observations suggest that absorption increases with molecular weight. However, measurements of sugars, polysaccharides, amino acids, and proteins yield no correlations of absorption with molecular weight within these groups. Therefore, it is concluded that absorption increases in these molecules with increasing molecular weight only in a threshold sense, with absorption increasing significantly only in a restricted molecular weight range. This range may approximate that observed for polyethylene glycol and dextran, viz., 1 to 100 monomer units. However, there is some indication that the transition range may be narrower than a factor of 100 in molecular weight.     

Acoustical investigations of a La<Subscript>0.75</Subscript>Sr<Subscript>0.25</Subscript>MnO<Subscript>3</Subscript> single crystal

The acoustical, resistive, and magnetic properties of a La_0.75Sr_0.25MnO₃ lanthanum manganite single crystal are investigated in the temperature range involving the second-order magnetic phase transition. The acoustical measurements are performed by the pulse-echo method in the frequency range 14–90 MHz. It is found that, as the temperature decreases, the velocity of a longitudinal acoustic wave propagating along the [111] axis in the single crystal drastically increases at temperatures below the critical point of the magnetic phase transition. No dispersion of the acoustic velocity is revealed. A sharp increase in the acoustic velocity is accompanied by the appearance of an acoustical absorption peak. The observed effects are discussed with due regard for the interaction of acoustic waves with the magnetic moments of the manganese ions.     

Ultrasonic attenuation and velocity properties in rat liver as a function of fat concentration: a study at 100 MHz using a scanning laser acoustic microscope

This study examines the extent to which ultrasonic attenuation coefficients and velocity properties change between normal and fatty rat liver. The view of this problem is toward the application in clinical medicine in the future. Fatty livers were produced in rats by feeding them alcohol diets in liquid form. The animals were sacrificed and the fat concentration of the liver specimens determined. The fat concentration varied from 2.5% to 16.8% wet weight. The ultrasonic attenuation coefficient and velocity properties in 28 specimens were measured at 100 MHz with the scanning laser acoustic microscope (SLAM). Regression analysis was applied to the liver's ultrasonic propagation properties as a function of fat concentration. The results show that the attenuation coefficient increases at a rate of 1.08 dB/mm/% fat and the velocity decreases at a rate of 2.3 m/s/% fat as the fat concentration increases.     

Influence of the porosity on the dispersion of the phase velocity of longitudinal acoustic waves in isotropic metal-matrix composites

The influence of the volumetric porosity of isotropic metal-matrix composite materials, which are reinforced with ceramic microparticles, on the dispersion of the phase velocity of longitudinal acoustic waves is investigated. For this purpose, the method of broadband acoustic spectroscopy with a laser source of ultrasound and piezoelectric detection of nanosecond ultrasonic pulses is used. Composite samples based on a silumin matrix with added silicon carbide (SiC) microparticles in different mass concentrations (3.8–15.5%) were investigated. As the concentration of SiC particles in a sample increases, its porosity that is determined using the hydrostatic-weighing method also increases. The simultaneous increase in the filler concentration and porosity leads to the appearance of a dispersion of the phase velocity of longitudinal acoustic waves in the sample within the frequency range of 3–25 MHz. The obtained empirical relationship between the relative change in the phase velocity and the sample porosity can be used to obtain a proximate quantitative estimate of the bulk porosity of the isotropic metal-matrix composite materials.     

Low-frequency spectroscopy of four-photon scattering of laser radiation in aqueous solutions of biopolymers

Four-photon scattering (FPS) spectroscopy is used to record rotational resonances of H₂O and H₂O₂ molecules in aqueous solutions of DNA and denatured DNA within a range of ±10 cm^-1 with a spectral resolution of 3 GHz. The resonance contribution of rotational transitions of these molecules in solutions was found to be considerably larger than that in distilled water. This fact is interpreted as a manifestation of the specific properties of a hydrate layer at the interface between water and DNA or denatured DNA molecules. An analysis of the FPS spectra shows that the concentration of H₂O₂ molecules in the hydrate layer of the DNA molecule increases threefold after denaturation. In addition, the FPS spectra of aqueous solutions of α-chymotrypsin protein with concentrations of 0-20 mg cm^-3 were measured in the spectral range of ±7 cm^-1. It is found that the velocity of hypersound in the protein aqueous solution, which is measured by the shift of the Mandelstam—Brillouin scattering spectrum components, is a cubic function of the concentration and reaches 3000 m/s at 20 mg/cm³.     

应用球形和海胆状金混合SERS基底检测高环多环芳烃

合成了海胆状金银复合纳米材料,并与球形金纳米材料混合作为表面增强拉曼活性基底实现了对水中高环多环芳烃的痕量检测。对海胆状材料进行表征,粒径大小约为300～400 nm,表面有40～100 nm明显的刺状凸起。与球形金溶胶混合后并优化pH值及混合比例等参数,产生了优于球形金溶胶2～3倍的增强效果。利用此增强基底检测了危害严重的高环多环芳烃污染物——芘(四环)、苯并蒽(四环)、苯并芘(五环),得到的光谱数据反映出混合SERS基底有良好的重复性和稳定性,对测得光谱进行特征峰归属分析,固体拉曼光谱与水溶液SERS光谱有确定的对应关系,并且在低浓度范围多环芳烃特征峰峰强与其水溶液浓度有良好的线性关系。经计算,芘(四环)、苯并蒽(四环)、苯并芘(五环)的检测限分别为0.44,2.92和1.64 nmol·L-1。该研究的创新点为合成了海胆金纳米颗粒,与球形金溶胶混合后制成新型高效SERS检测基底;选用自制高效SERS基底,实现了高环PAHs痕量检测。结果表明,利用该方法制备的活性基底,可实现对水中高环多环芳烃的痕量检测,为检测水中高环多环芳烃提供了实验室依据。     

聚乙烯醇水溶液二维定向凝固的微观组织演化

为了深入探究定向多孔聚合物材料的微观组织形成机理,利用定向凝固原位实时观察手段,研究不同浓度及不同分子量聚乙烯醇(PVA)水溶液在不同抽拉速度下的定向凝固形貌演化.PVA水溶液的定向凝固形态在低浓度(1 wt%,2.5 wt%)和小分子量(M_w=24000)情况下,一次枝晶间距随着抽拉速度的增加而减小.随着PVA浓度和分子量的增加,一次枝晶间距随抽拉速度变化不明显,枝晶主轴尺寸则随速度增加呈现减小的趋势.与传统凝固形态形成机理相比,PVA水溶液的凝固形态由PVA分子的扩散引起的凝固界面不稳定性机理和PVA高分子链交联引起的局部相分离机理竞争决定.     

Kinetics of nitrous acid formation in nitric acid solutions under the effect of power ultrasound

Sonochemical nitrous acid formation was investigated in 0.1-4.0 mol dm(-3) aqueous nitric acid solutions under the effect of power ultrasound with 20 kHz frequency. HNO2 steady-state concentration was obtained under long-time sonication; the excess HNO2 formed is decomposed and evoluted from the solution as NO and NO2 gases. The HNO2 steady-state concentration and the HNO2 initial formation rate depend linearly on the HNO3 concentration and acoustic intensity (1.8-3.5 W cm(-2)) and decrease with rising temperature in the range 21-50 degrees C. The HNO2 formation rate depends on the type of saturating gas as follows: Ar > N2 > He > air. NO and O2 are the major gaseous products of HNO3 sonication. The NO2 accumulation of in the gas phase is observed only when the decomposition of HNO2 formed becomes noticeable. The gaseous products formation rates depend on the HNO3 concentration, acoustic intensity and the type of saturating gas. The mechanism of HNO2 sonochemical formation is assumed to be the thermal decomposition of HNO3 in the gaseous vicinity of collapsing bubbles or in the overheated liquid reaction zone surrounding the cavitational bubbles.     

Volumetric, viscometric, acoustical, and optical studies of glutamic acid in aqueous zinc and copper chloride solutions

Ultrasonic velocity, density, viscosity and refractive index measurements of L-glutamic acid in aqueous zinc chloride and copper chloride solutions have been carried out at 303.15K. From these experimental data isentropic compressibility, acoustic impendence, relative association, free path length, apparent molar volume, apparent molar isentropic compressibility and molar refraction of L-glutamic acid in aqueous solutions of electrolytes are evaluated. These values have been used to explain molecular association, solutesolvent interaction through hydrogen bonding and solvation. Viscosity data have been analyzed in the light of Jones-Dole equation and the constants A and B have been estimated and interpreted in terms of ion-ion, ionsolvent and molecular interactions occurring in solutions.     

Surface response of a viscoelastic medium to subsurface acoustic sources with application to medical diagnosis

The response at the surface of an isotropic viscoelastic medium to buried fundamental acoustic sources is studied theoretically, computationally and experimentally. Finite and infinitesimal monopole and dipole sources within the low audible frequency range (40-400 Hz) are considered. Analytical and numerical integral solutions that account for compression, shear and surface wave response to the buried sources are formulated and compared with numerical finite element simulations and experimental studies on finite dimension phantom models. It is found that at low audible frequencies, compression and shear wave propagation from point sources can both be significant, with shear wave effects becoming less significant as frequency increases. Additionally, it is shown that simple closed-form analytical approximations based on an infinite medium model agree well with numerically obtained "exact" half-space solutions for the frequency range and material of interest in this study. The focus here is on developing a better understanding of how biological soft tissue affects the transmission of vibro-acoustic energy from biological acoustic sources below the skin surface, whose typical spectral content is in the low audible frequency range. Examples include sound radiated from pulmonary, gastro-intestinal and cardiovascular system functions, such as breath sounds, bowel sounds and vascular bruits, respectively.     

Concentration dependence of the hypersonic velocity dispersion in aqueous solutions of 4-methylpyridine

The hypersonic velocity dispersion in aqueous solutions of 4-methylpyridine in the frequency range from 4.7 to 6.1 GHz has been studied by Brillouin scattering spectroscopy. A negative hypersonic velocity dispersion is established for solutions with concentrations of 0.08 and 0.06 molar fractions of 4-methylpyridine.     

Self-diffusion coefficients and orientational correlation times in aqueous NaCl solutions: Complementarity with structural investigations

The dynamical properties of pure water and aqueous NaCl solutions over a wide range of salt concentrations (0-6 m) at ambient conditions are characterized by molecular dynamics (MD) simulations. MD simulations are performed with a flexible SPC water model as a solvent, while the ions are treated as charged Lennard-Jones particles. In this paper, attention has been focused on the self-diffusion coefficients (D_i) of ions and water molecules and on orientational correlation time of water molecules. It is found that the self-diffusion coefficients decrease with ion concentration. Moreover, the self diffusion coefficients of sodium and chloride at higher salt concentrations are very comparable which may be due to the formation of clusters of these ions. The deduced rotational dynamics speeds up as the salt concentration increases. Some complementarities between dynamical properties and structural ones, recently obtained, are carried out.     

重塑砂质含气沉积物的声响应特性与模型预测分析

海洋沉积物中气泡的存在对沉积物的声学特性有显著影响.为实现在实验室内对不同初始应力条件下含气沉积物的声学特性测量,研制了一套可用于土工三轴仪的双探针声学测量系统,基于CT扫描试验获得重塑含气砂样品中气泡群的尺寸分布,确定其共振频率范围.试验结果表明:细砂沉积物声速随气体含量的增加呈指数型降低,衰减系数随气体含量的增加呈...     

Magnetic field dependence of spin-lattice relaxation enhancement using piperidinyl nitroxyl spin-labels

We examined the magnetic resonance properties of 12 paramagnetic piperidinyl nitroxyls in water and plasma solutions. Paramagnetic contributions to proton relaxation times were measured using 10.7 and 100 MHz spectrometers. Proton relaxation enhancement from nitroxyls increased with ascending molecular weight, in plasma solutions versus equimolar aqueous solutions, and with measurements at 10.7 MHz compared to 100 MHz. Relaxation rates were observed to approximately double at 10.7 MHz compared to 100 MHz and from water to plasma solutions. The data indicate that proton spin-lattice relaxation enhancement is magnetic field-dependent, and increases using nitroxyls of large molecular weight and with chemical substitutents that increase the microviscosity of solvent water molecules. The development of nitroxyls for diagnostic MRI will be aided by understanding these in vitro physical characteristics and trends.     

基于混合气体分子复合弛豫模型的一氧化碳浓度检测算法

研究了声波通过混合气体时,复合弛豫声吸收和声速与气体各成分浓度和声频率之间的依赖关系.以一氧化碳气体、水蒸气、氮气和氧气的混合气体为例,分别建立了弛豫声吸收和声速与气体浓度的三维模型,以及弛豫声吸收与声频率的二维模型.完成了通过测量弛豫声吸收和声速计算一氧化碳气体浓度的算法推导,提出了一种依据弛豫声吸收和声速检测气体浓度的简化算法.仿真实验结果不仅证明了算法的理论可行性,还给出了算法的最佳适用声频率范围,并估计了将算法应用于实验的误差原因,证明了算法具有实际可行性. 关键词： 气体浓度声学检测 一氧化碳浓度检测 复合弛豫声吸收 声速     

温度相关的微波频率下氯化钠水溶液介电特性

针对NaCl水溶液(0.001–0.5 mol/L)介电特性, 实验调查了频率(200–6.25 GHz), 温度(293–353 K)、 浓度相关复介电常数. 结果表明: 频率增大的过程中虚部呈逐渐减小的趋势, 高温使离子扰动增大, 破坏了溶液内部水分子四面体结构和氢键构象而使介电常数实部减小. 与纯水相比, 溶液的损耗角正切在高温353 K低频区下降明显. 同时发现2.45和5.8 GHz的复介电常数随温度变化的温度窗效应, 温度窗效应导致微波加热时耗散功率的振荡变化, 温度分布不均匀现象在实验中得以证实. 关键词： 微波 复介电常数 介电特性 高温探头     

Effects of dust size distribution in ultracold quantum dusty plasmas

The effect of dust size distribution in ultracold quantum dusty plasmas are investigated in this paper. How the dispersion relation and the propagation velocity for the quantum dusty plasma vary with the system parameters and the different dust distribution are studied. It is found that as the Fermi temperature of the dust grains increases the frequency of the wave increases for large wave number dust acoustic wave. The quantum parameter of H_d also increases the frequency of the large wave number dust acoustic wave. It is also found that the frequency ω₀ and the propagation velocity v₀ of quantum dust acoustic waves all increase as the total number density increases. They are greater for unusual dusty plasmas than those of the usual dusty plasma.