含相变微粒流体热对流启动的Galerkin解

采用Bubnov-Galerkin方法对有恒壁温条件下,两平板间夹有含相变颗粒流体的自然对流热启动瑞利数进行了近似解析求解,求出了临界瑞利数Racr和波频数kcr随相变物质浓度,以及在相变温度范围内随加热表面温度的解析关系表达式.从而,为实现该类功能性潜热流体的自然对流传热强化,及其优化控制蓄热过程有理论指导意义.     

微重力条件下流体相变和临界现象

研究流体相变及临界现象对今后化学工程的发展有重大意义．由于各种具有临界点的体系在各自 临界点有一些共同的实验特征和极相似的临界现象，而流体的研究在实验上又有独特方便之处，所以可 作为普适性研究将理论及实验结果推广到固体．微重力条件下的流体相变及临界现象研究提供了十分 靠近临界点的最佳实验条件，本文介绍了这方面研究工作的物理意义及进展．     

固液黏着功的Berthelot平均规则的推广及应用

以固液黏着功的Berthelot几何平均规则及其推广为基础的Zisman方程、Fowkes方程和Owens-Wendt方程是固体表面张力测定的基础.对Berthelot几何平均规则进行了进一步的推广,并以此为基础,对Zisman方程中的参数给出了推广的表示式,并对Fowkes方程和Owens-Wendt方程进行了进一步的推广.关键词：接触角Berthelot规则Fowkes方程Owens-Wendt方程     

GaAs相变和热力学性质的密度泛函理论研究

利用平面波赝势密度泛函方法,对GaAs从闪锌矿结构到CsCl 结构的相变进行了理论研究.通过Birch-Murnaghan状态方程拟合闪锌矿结构GaAs的能量和体积,得到了GaAs的热力学性质.我们发现对 GaAs来说,闪锌矿结构通常比CsCl结构稳定,由闪锌矿结构到CsCl结构的相变压力在37.019 GPa左右.计算所得到的晶格常数、体弹模量及体弹模量对压强的一阶导数与实验值以及其他作者的计算值相符合.     

高压下CaPo弹性性质和热力学性质的第一性原理研究

利用密度泛函理论的平面波赝势方法预测研究了CaPo从岩盐结构(B1结构)到氯化铯结构(B2结构)的相变以及B1结构CaPo高压下的弹性性质以及热力学性质等.通过等焓原理发现B1→B2的相变压力为22.8GPa. 同时计算了B1结构CaPo高压下的弹性常数以及剪切模量、杨氏模量等相关弹性参数,结果发现当压力超过20GPa时,B1结构CaPo开始不稳定了,这和等焓原理所得结果相符合. 最后通过Debye模型成功获取了B1结构C关键词：相变弹性性质热力学性质CaPo     

纳米流体振荡热管内部流动和传热特性

本文以纳米流体和去离子水的振荡热管作为研究对象,通过实验的方法,运用可视化的加热与观测手段,对比纳米流体和去离子水振荡热管的内部工质流型和冷热端温差,发现纳米颗粒体积浓度达到一定浓度后,相对于去离子水,纳米流体可以降低振荡热管的下极限热流,提高上极限热流,而后者足利用纳米流体为工质改进振荡热管性能主要特点,内在物理实质是纳米流体具有明显不同的流型转变.     

具有不同作用势的两平行墙间流体的浸润相变

用解析方法讨论了当两平行墙对流体施加不同的作用势时流体的浸润相变。系统的状态很敏感地依赖于两墙的作用势和两墙间距离的大小。即使两墙差别很小,在一定条件下仍可发生浸润一墙而不浸润另一墙的现象。系统中发生的浸润相变可能是一级的,也可能是二级的。关键词：     

三层流体界面内波的二阶Stokes解

以小振幅波理论为基础,利用摄动方法研究了三层密度成层状态下的界面内波,求得了三层成层状态下各层速度势的二阶渐近解及界面内波波面位移的二阶Stokes解.结果表明：一阶解为正弦波解,与传统线性理论的结果相一致;二阶解描述了界面波的二阶非线性修正及两界面波之间的非线性相互作用;一阶解及二阶解都依赖于各层流体的厚度及密度.Umeyama导出的理论结果为本文的特殊情形.关键词：三层密度成层流体内波二阶Stokes解小振幅波理论     

热力参数的对比变换与流体工质热力性质的通用对比方程

本文提出了判别流体热力学性质的通用对比方程的规则和选择作为通用对比方程的热力学参数对比交换的方法;具体给出了工质饱和液体焓和温度的合适对比变换式和通用对比方程。经检验,该通用方程的计算值与２５种常用流体工质的推荐值的平均绝对偏差为０．５％,算术平均偏差为－０．０４％。本文的理论纠正了传统的只用临界参数为对比值的片面认识,为建立在无通用对比方程而仅利用合适的参数变换,从一种已知物性物质推算另一种物质未知物性的一般方法和其它物性的通用对比方程奠定了基础。     

相变与临界乳光现象

分别采用白炽聚光灯和氦氖激光器照射,观察六氟化硫在临界点附近的临界乳光现象.     

Critical Behavior of Liquid 3He

We investigate the liquid–gas second-order phase transition in liquid ³He using the variational calculations based on the cluster expansion of the energy functional. We also compute the critical point exponents of liquid ³He that are in agreement with experimental data.     

相互作用玻色子模型中振转过渡区的特征研究

详细研究了相互作用玻色子模型中U(5)振动极限到SU(3)转动极限的相变行为.通过对能谱和E2跃迁强度等的分析,说明了在临界点的核具有最大的非刚性. Transitional patterns from the U(5) vibrational limit to the SU(3) rotational limit in the interacting Boson model are studied in detail. The transitional behavior of low-lying energy levels, isomer shifts, E2 transition rates, and some other related quantities across the entire region are investigated. The results show that nuclei in the critical region are most non-rigid.     

改进的PNJL模型下QCD的相图

Polyakov-Nambu-Jona-Lasinio（PNJL）模型是研究强相互作用物质性质的使用最为广泛的有效模型之一。在PNJL模型的基础上考虑了手征凝聚和Polyakov圈之间的纠缠作用,并且引入了化学势修正的Polyakov有效势,由此得到了化学势依赖的entangled PNJL（μEPNJL）模型。在平均场框架下的计算结果表明:相较于原始的PNJL模型,由μEPNJL模型计算得到的临界点（CEP）朝着温度更高、化学势更小处移动,并且手征对称性恢复相变和退禁闭相变在较大的化学势范围内都重合得很好。通过与STAR合作组在相对论重离子对撞机（RHIC）上进行的净质子数分布的测量结果相比,可以发现,通过适当的参数调节,由μEPNJL模型计算得到的CEP更加靠近实验预言的CEP可能存在的区域。Polyakov-Nambu-Jona-Lasinio (PNJL) model is one of the most popular effective quark models to investigate the properties of strongly interacting matter. Based on the PNJL model, we consider the entanglement interactions between the chiral condensate and Polyakov-loop, as well as the chemical potential modification of Polyakov-loop potential simultaneously, which is named μEPNJL model. Compared with the original PNJL model, the calculations in the mean field approximation show that the critical end point (CEP) given in the μEPNJL model moves towards higher temperature and smaller chemical potential in the T-μ phase diagram. Besides, the chiral symmetry restoration and deconfinement phase transition coincide well in a wide range of chemical potential. Comparing our calculations with the measurement of the moments of net-proton multiplicity distributions at Relativistic Heavy-Ion Collider (RHIC) by STAR Collaboration, we find that the CEP given by μEPNJL model can be closer to the range predicted by the experiment through appropriate parameter adjustment.     

Phase separation, ferromagnetism and magnetic irreversibility in La1−xSrxMn1−yFeyO3

Magnetic susceptibility, χ(T), is investigated in ceramic La_1−xSr_xMn_1−yFe_yO₃ (LSMFO) samples with x=0.3 and y=0.15−0.25. A ferromagnetic (FM) transition observed in LSMFO is accompanied with an appreciable decrease of the transition temperature with increasing y, which is connected to breaking of the FM double-exchange interaction by doping with Fe. Strong magnetic irreversibility, observed in low (B=10 G) field, gives evidence for frustration of the magnetic state of LSMFO. The FM transition, which is expanded with increasing B, is more pronounced in the samples with y=0.15-0.20 and broadens considerably at y=0.25, where the irreversibility is increased. Well above the transition, χ(T) exhibits a Curie-Weiss asymptotic behavior, yielding very large values of the effective Bohr magneton number per magnetic ion, incompatible with those of Mn or Fe single ions. At y=0.15 and 0.20 a critical behavior of χ⁻¹(T)∼(T/T_C−1)^γ in the region of the FM transition is characterized by influence of two different magnetic systems, a 3D percolative one with γ₌γ_p≈1.8 and T_C=T_C^(p), and a non-percolative 3D Heisenberg spin system, with γ=γ_H≈1.4 and T_C=T_C^(H), where T_C^(p)<T_C^(H). At y=0.25 the percolative contribution to the critical behavior of χ(T) is not observed. The dependence of χ on T and y gives evidence for phase separation, with onset already near the room temperature, leading to generation of nanosize FM particles in the paramagnetic host matrix of LSMFO. The ferromagnetism of LSMFO is attributable to percolation over the system of such particles and generation of large FM clusters, whereas the frustration is governed presumably by a system of smaller weakly-correlated magnetic units, which do not enter the percolative FM clusters.     

Liquid-liquid phase transition in water

Water shows anomalies different from most of other materials.Different sceniaros have been proposed to explain water anomalies,among which the liquid-liquid phase transition(LLPT)is the most discussed one.It attributes water anomalies to the existence of a hypothesized liquid-liquid critical point(LLCP)buried deep in the supercooled region.We briefly review the recent experimental and theoretical progresses on the study of the LLPT in water.These studies include the discussion on the existence of the first order LLPT in supercooled water and the detection of liquid-liquid critical point.Simulational results of different water models for LLPT and the experimental evidence in confined water are also discussed.     

光学多稳系统的相变及临界点分类

参照朗道相变理的基本精神,确定光学多稳性系统的相变与临床界现象,揭示了相变的多样性,以及多稳系统通向完全单稳状态态的不同路径。多稳性的级次愈高,相变的式样也就愈多。     

采用正方元胞的Ising模型实空间重正化群解

在二维正方形晶格上,将元胞取为4格点正方形,采用3种不同的规则定义块自旋状态,进行了重正化群计算,得出了更为精确的结果;解决了元胞内格点数为偶数的重正化群计算问题.     

Ward's identity in critical dynamics

We consider the relaxation of an order-parameter fluctuation of wave numberk in a system undergoing a second-order phase transition. In general, close to the critical point, wherek ^{–1 –1} (the correlation length) the relaxation rate has a linear dependence on/k of the form (k, ) = (k, 0)x(1–a/k). In analogy with the use of Ward's identity in elementary particle physics, we show that the numerical coefficienta is readily calculated by means of a mass insertion. We demonstrate, furthermore, that this initial linear drop is the main feature of the full/k dependence of the scaling functionR ^–x (k,), wherex is the dynamic critical exponent andR=(k²+ ²)^1/2 is the distance variable.