饱和砂岩的滞弹性弛豫衰减特征及微观机理的探索

应用Metravib热机械分析仪,以饱和岩石进行正弦波加载的方式, 分别对三种不同孔隙度的泵油饱和彭山砂岩、泵油和甘油饱和自贡长石砂岩进行了衰减实验研究,得到衰减的热弛豫规律.据此规律求得它们的激活能和原子振动频率, 其激活能和原子的振动频率比间隙原子的激活能和振动的频率低, 此现象用饱和砂岩中产生的缺陷原子簇的整体振动比单个或孤立的原子的振动频率低做出了解释. 在饱和岩石的晶粒间界缺陷处参与扩散的是固体原子、液体及气体原子. 并得出随孔隙度和黏滞系数增大,衰减强度和激活能增大,原子的振动频率增高,弛豫时间减小的结论. 在正弦波应力作用下,由多种矿物晶体胶结而成的饱和砂岩是一种多晶、多相的固体, 由于内部结构复杂、缺陷广布,产生弛豫衰减是普遍现象.砂岩中存在点缺陷、位错、 晶界及孪晶界面等许多缺陷及缺陷间的相互作用都可以产生弛豫型衰减峰. 用饱和砂岩中特有的饱和液体及砂岩内部结构的复杂性解释了饱和砂岩的衰减机理, 很自然地将其宏观衰减特征与微观结构紧密连在一起.饱和砂岩中的各种缺陷、 相界等会导致多重弛豫,使它们的弛豫衰减峰变宽,分布参数增大.这项研究既具有理论意义,也具有实用价值.     

基于Biot-喷射流统一模型Maxwell流体饱和孔隙介质中的弹性波

推广Biot-Tsiklauri声学模型的同时借鉴Dvorkin和Nur的工作,建立了具有任意孔径分布并顾及喷射流动机制的非牛顿流体饱和孔隙介质声学模型,研究了非牛顿流体(Maxwell流体)饱和孔隙介质中的弹性波的衰减和频散特性.着重讨论充孔隙Maxwell流体的非牛顿流效应对弹性波的频散和衰减的影响.研究表明,饱和流体的非牛顿流效应和喷射流动机制均是引起弹性波波频散和衰减的重要因素.依据非牛顿流体(Maxwell流体)饱和各向同性孔隙介质的Biot-喷射流声学模型,喷射流动只影响纵波的频散和衰减,而饱和流体的非牛顿流效应不仅影响纵波,而且还影响横波的频散和衰减.     

非晶态快离子导体(AgI)_x(Ag_4P_2O_7)_(1-x)的声学性质

用液氮骤冷方法制备了(AgI)_x(Ag_4P_2O_r)_(1-x)系列非晶态快离子导体。对AgI摩尔浓度x=0.50,0.60,0.67,0.75,0.80的样品,在77—300K温度范围及2,5,10,15MHz的频率上测量了纵波和横波的超声衰减和声速。发现在200—240K附近存在一个异常强的弛豫型超声吸收峰,随AgI含量的增加,该峰的位置向低温方向移动,且峰的高度增大。在实验的温度范围内,观察到纵波和横波的内耗Q_M~(-1)基本相等。由声速与AgI浓度关系的实验结果,计算了样品的弹性常数,并分析了玻璃态结构的变化。 用Ngai提出的低频涨落、耗散和弛豫过程的统一理论(即红外发散响应(IDR)理论),对实验结果进行了较满意的解释,给出了样品的表观激活能和红外发散指数。     

KLiSO_4单晶的电学性质

我们证实了KLiSO_4为Li离子导体。通过测定样品中的电位分布,确定其载流子为间隙Li离子和Li空位。其电流弛豫在一定时域内遵从负幂次衰减规律。与之对应,在一定频域内存在与频率成负幂次关系的介电色散。在相变温度附近,本底电流、直流电导率和表观介电常数除发生跃变外还出现一个尖锐的小峰。此峰只有在变温速率较慢时才能观察到,表明该相变具有弛豫过程。     

被孔隙介质约束的弹性杆中的导波*

为了研究导波在被孔隙介质约束的弹性杆结构中的传播规律,分析孔隙参数对导波传播特性的影响,本文建立了无限大孔隙介质包裹圆柱体的理论模型,利用孔隙介质弹性波动理论,分析了导波的频散曲线,以及圆柱半径和孔隙参数对于导波传播特性的影响。结果表明,在该结构中传播的纵向导波存在频散特性。内部圆柱半径的改变影响波导结构,从而影响导波传播。外部孔隙介质的渗透率对于导波频散的影响较小,孔隙度的改变影响孔隙介质体波波速,从而影响导波频散曲线的截止频率。同时,导波存在较小的衰减,且衰减随孔隙度增大而增大。这些结果对于后续开展无限大介质包裹弹性杆结构的超声无损评价提供了一定的理论参考。     

KLiSO4单晶的电学性质

我们证实了KLiSO₄为Li离子导体。通过测定样品中的电位分布,确定其载流子为间隙Li离子和Li空位。其电流弛豫在一定时域内遵从负幂次衰减规律。与之对应,在一定频域内存在与频率成负幂次关系的介电色散。在相变温度附近,本底电流、直流电导率和表观介电常数除发生跃变外还出现一个尖锐的小峰。此峰只有在变温速率较慢时才能观察到,表明该相变具有弛豫过程。 关键词：     

千周和兆周范围的马氏体相变内耗以及预马氏体相变内耗

在千周和兆周两个频段分别测量了含Cd为46.1at％,47.5at％,50.0at％和52.5at％的AuCd合金中与马氏体转变有关的内耗和杨氏模量。实验结果表明,在千周范围,由于马氏体转变引起的Q^-1(内耗)是静滞后型的。Q^-1峰的形成可以用弹性软化及界面位错的静滞后阻尼机制来解释。而兆周范围的超声衰减是与频率有关的,表明尚有共振型及弛豫型阻尼的成份。此外,实验还观察到AuCd合金的等温马氏体转变Q^-1峰以及预马氏体相变Q^-1峰。 关键词：     

在玻璃转变温度及其以上温区聚苯乙烯/聚氧化乙烯共混物的动力学弛豫行为

用熔融共混法制备了不同组分的聚苯乙烯(PS)与聚氧化乙烯(PEO)共混物(PS/PEO).在玻璃转变温度T_g及其以上温区,利用相对能量耗散技术研究了该共混物的动力学行为.结果发现,在能量耗散-温度曲线上出现了两个弛豫型的耗散峰(α峰和α′峰).分析表明,α峰是与PS玻璃转变有关的特征耗散峰; α′峰则对应于一种“液-液转变”.两者的弛豫时间τ都不满足Arrhenius关系.此外,还研究了组分对这两个弛豫型耗散峰的影响,并给予了定性的解释. 关键词： 相对能量耗散 玻璃转变 力学弛豫     

气泡线性振动对含气泡水饱和多孔介质声传播的影响

为了研究孔隙水含少量气泡时多孔介质中波的传播,本文在Biot模型的基础上,将孔隙水中气泡的体积振动融合到多孔介质的孔隙流体渗流连续性方程中,从而得到了考虑气泡体积振动的孔隙流体渗流连续性方程.在此基础上,根据气泡线性振动下气泡瞬时半径和介质背景压力的关系,以及多孔介质运动方程和流体介质运动方程,导出了受气泡影响下多孔介质位移矢量波动方程,建立了非水饱和多孔介质声速频散和衰减预报模型.气泡的存在增大了孔隙水的压缩率,导致含气泡水饱和多孔介质声速的降低.当声波频率等于气泡的共振频率时,在声波激励下,介质呈现高频散,且孔隙水中的气泡产生共振,吸收截面达到最大,使得多孔介质的声衰减也达到最大.文中数值分析验证了上述结论,表明了气泡含量、大小和驱动声场频率是影响声波在含少量气泡的水饱和多孔介质中传播的主要因素.     

国产室温硫化硅橡胶的声学特性

本工作测量了国产室温硫化硅橡胶十个品种的纵波和拉伸波波速与衰减常数,考察了频率和温度对纵波波速的影响,并将其性能与常规透声橡胶进行了比较.研究表明,这些室温硫化硅橡胶的纵波衰减常数,声速频散和温度系数明显低于常规透声橡胶,并且有与液体十分相近的泊松比.     

Relaxation process in chitosan–oxalic acid solid polymer electrolytes

We investigate the room temperature frequency dependence of electrical modulus for the polymer electrolytes consisting of chitosan and oxalic acid in the frequency range from 50 Hz to 1 MHz. Oxalic acid serves as the proton provider. It is found that the lowest imaginary electrical modulus is shown by the highest conducting sample OA40, which contains 60 wt.% chitosan and 40 wt.% oxalic acid. The electrical moduli for OA40 sample membrane at different temperatures are also studied, and the peak of the imaginary electrical modulus has been observed to shift towards higher frequency with increasing temperature. This indicates that relaxation is thermally assisted. Analysis of electrical modulus shows that the main relaxation process in chitosan–oxalic acid polymer electrolyte system is a non-Debye process associated with viscoelastic relaxation.     

Measurement of orientation crystallization rates of linear polymers by means of dynamic X-ray diffraction technique. II. Frequency dispersion of strain-induced crystallization coefficient of natural rubber vulcanizates in subsonic range

The orientation crystallization behavior of natural rubber vulcanizates was investigated by means of a dynamic X-ray diffraction technique utilizing the half-circle sector technique. The frequency dependence of dynamic diffraction intensities from diatropic and paratropic crystal planes, (002) and (200) planes, was observed over a frequency range from 10^?3 to 10¹ Hz as a function of temperature, degree of cross-linking, static extension ratio, and dynamic strain amplitude.

The frequency dependence of the dynamic X-ray diffraction gives two dispersion regions around 10^?2 and 10^?1 Hz. The phase angle between the dynamic X-ray diffraction and dynamic strain of a bulk specimen is definitely positive; i.e., the dynamic strain of the specimen is always behind the dynamic orientation crystallization.

The frequency dispersion at low frequencies, around 1WZ Hz is very obvious for the (200) crystal plane and shifts somewhat to higher frequencies under those conditions that increase the mobility of self-diffusion of rubber molecules, i.e., increase of temperature and decreases of extension ratio and degree of cross-linking. The frequency dispersion at high frequencies, around 10¹ Hz, is rather obvious for the (002) crystal plane and does not shift appreciably under the experimental conditions.     

AC conductivity and dielectric relaxation in Ba(Sm1/2Nb1/2)O3 ceramic

The complex perovskite oxide a barium samarium niobate (BSN) synthesized by solid-state reaction technique has single phase with cubic structure. The scanning electron micrograph of the sample shows the average grain size of BSN∼1.22 μm. The field dependence of dielectric response and loss tangent were measured in the temperature range from 323 to 463 K and in the frequency range from 50 Hz to 1 MHz. The complex plane impedance plots show the grain boundary contribution for higher value of dielectric constant in the low frequency region. An analysis of the dielectric constant (ε′) and loss tangent (tan δ) with frequency was performed assuming a distribution of relaxation times as confirmed by the scaling behaviour of electric modulus spectra. The low frequency dielectric dispersion corresponds to DC conductivity. The logarithmic angular frequency dependence of the loss peak is found to obey the Arrhenius law with an activation energy of 0.71 eV. The frequency dependence of electrical data is also analyzed in the framework of conductivity and electric modulus formalisms. Both these formalisms show qualitative similarities in relaxation times. The scaling behaviour of imaginary part of electric modulus M″ and dielectric loss spectra suggest that the relaxation describes the same mechanism at various temperatures in BSN. All the observations indicate the polydispersive relaxation in BSN.     

Energy of the elastic loading of anharmonic solids

This paper reports on the results of measurements of changes in the temperature of a solid under the adiabatic elastic loading (thermoelastic effect), the coefficient of thermal expansion, and the Young’s modulus of a rigid-chain vitrified polymer, namely, polyimide. It has been found that there are differences in the sign and magnitude of the changes in the energy of thermal origin in samples and the work of the external force. The energy of the thermoelastic effect has been explained in terms of the influence exerted by the anharmonic expansion of a solid, with the separation of the quasi-static potential and dynamic components of the thermal energy of the solid. The loading with an external force causes a redistribution of the thermal energy. A change in the temperature of the solid corresponds to a change in the dynamic component. An energy analysis of the adiabatically loaded anharmonic oscillator has confirmed the conclusion regarding the mechanism of energy transfer and revealed that, under loading, there is a redistribution of the kinetic and potential components of the internal energy of the oscillator.     

Relaxation processes in the paraelectric phase of ceramic oxides with a perovskite structure

Solid solutions of barium, strontium, and lead titanate ceramics with a perovskite structure are studied using impedance spectroscopy in the frequency range 10²–10⁶ Hz at temperatures from 20 to 450°C. The experimental data represented by the dispersion of the electric modulus are compared with the results of calculations performed for different mechanisms of the non-Debye relaxation in terms of the Havrilyak-Negami empirical formulas and the Jonscher universal dielectric response with the aim of determining a more adequate approach. The activation energy of relaxation processes in the paraelectric phase of the samples under investigation are calculated.     

外场作用下聚合物滞后生热效应

为了研究振动参数对聚合物黏弹性能及塑化成型过程的影响,深入分析了振动场的作用机理,揭示了相位角与滞后生热率之间的关系,得出了振动场作用下聚合物塑化成型速率表达式,最后通过聚对苯二甲酸乙二醇酯(PET)动态毛细管挤出以及多维振动塑化成型设备进行实例计算和实验研究,实验结果和理论计算值符合得很好,并得出结论: PET塑化速率随振动频率的增加呈先增加后减小的趋势,当激振频率趋向于材料固有频率时(振动频率约为15 Hz时),PET塑化速率达到最大值,当振幅为6 MPa时,其值约为22 g/min,为相同振幅下,频 关键词： 振动场 滞后生热 相位角 低温成型     

聚乙烯/银纳米颗粒复合物的分子动力学模拟研究

通过分子动力学模拟对聚乙烯/银纳米颗粒复合物的结构、极化率和红外光谱、热力学性质、力学特性进行计算, 分析其随模拟温度和银颗粒尺寸的变化规律. 模拟结果表明: 聚乙烯/银纳米颗粒复合物为各向同性的无定形结构, 温度升高可提高银纳米颗粒的分散均匀性; 银纳米颗粒表面多个原子层呈现无定形状态, 并在银颗粒和聚乙烯基体的界面形成电极化层, 界面区域随颗粒尺寸和温度的增加分别减小和增加; 与聚乙烯体系相比, 聚乙烯/银纳米颗粒复合物的极化率高很多, 且随温度的升高和银颗粒尺寸的减小而增大; 银颗粒尺寸直接影响界面电偶极矩的强度和振动频率, 红外光谱峰强度和峰位随颗粒尺寸发生变化; 聚乙烯/银纳米颗粒复合物具有比聚乙烯体系更高的等容热容和与聚乙烯体系相反的负值热压力系数, 热容随颗粒尺寸的变化较小, 但随温度的升高而明显减小, 具有显著的温度效应; 热压力系数随温度的变化较小, 但随颗粒尺寸的增加而减小, 具有明显的尺度效应, 温度稳定性更好; 聚乙烯/银纳米颗粒复合物的力学特性表现出各向同性材料的弹性常数张量, 具有比聚乙烯体系更高的杨氏模量和泊松比, 并且都随温度的升高和银颗粒尺寸的增大而减小, 加入银纳米颗粒可有效改善聚乙烯的力学性质. 关键词： 分子动力学模拟 聚合物纳米复合物 纳米颗粒     

Dynamic mechanical relaxation and loss in the incommensurate phase of quartz

The dynamic mechanical properties of quartz have been studied as a function of temperature across the α-β phase transition and in the vicinity of the incommensurate (IC) phase on cooling from the β phase. The mechanical response of the IC phase shows strong anelasticity for measurement of Young's modulus (closely related to C(11) in our geometry) with modulated stress driven at 1 Hz. The dynamic shear modulus does not show similar strong effects in its imaginary component, although a very weak anomaly is barely detectable in the real part of the modulus. Our results indicate that the incommensurate microstructures within the quartz transition interval are susceptible to dilatational stress with relaxation times around 1 s.