Denolf Katleen, Cordoyiannis George, Glorieux Christ, Thoen Jan
Laboratorium voor Akoestiek en Thermische Fysica, Departement Natuurkunde en Sterrenkunde, Katholieke Universiteit Leuven, Celestijnenlaan 200D, bus 2416, B-3001 Leuven, Belgium.
Phys Rev E Stat Nonlin Soft Matter Phys. 2007 Nov;76(5 Pt 1):051702. doi: 10.1103/PhysRevE.76.051702. Epub 2007 Nov 7.
The effect of the nonmesogenic solutes cyclohexane (CH), biphenyl (BP), and water (W) on the nematic-isotropic (N-I) and the nematic-smectic- A (N-SmA) phase transitions in the liquid crystal octylcyanobiphenyl (8CB) has been studied by means of adiabatic scanning calorimetry. For BP and CH a linear decrease of both transition temperatures was observed with increasing solute mole fraction. For water the transition temperature stayed nearly constant (after a slight decrease for mole fractions of water up to 0.1) over the entire investigated region. For all concentrations of biphenyl and water studied the N-SmA transition remains second order. For 8CB+CH, however, crossover from second order to first order is observed at a tricritical point of the mole fraction x of CH around 0.046. For water it was found that for mole fractions of water above 0.1 phase separation between an 8CB rich and a water rich phase occurred. The changes in the transition temperatures and differences between the three systems, and in particular the crossover from second order to first order in the 8CB+CH system, is explained in terms of a mean-field free energy density expression including coupling terms of the solutes mole fraction with the nematic and smectic- A order parameters.
通过绝热量热法研究了非介晶溶质环己烷(CH)、联苯(BP)和水(W)对液晶辛基氰基联苯(8CB)向列相-各向同性相(N-I)和向列相-近晶A相(N-SmA)相变的影响。对于BP和CH,随着溶质摩尔分数的增加,两种转变温度均呈线性下降。对于水,在整个研究区域内,转变温度几乎保持恒定(在水的摩尔分数达到0.1之前略有下降)。对于所研究的所有联苯和水的浓度,N-SmA转变仍为二级相变。然而,对于8CB+CH,在CH的摩尔分数x约为0.046的三临界点处观察到从二级相变到一级相变的转变。对于水,发现当水的摩尔分数高于0.1时,会出现富含8CB的相和富含水的相之间的相分离。根据平均场自由能密度表达式,包括溶质摩尔分数与向列相和近晶A序参量的耦合项,解释了三种体系转变温度的变化和差异,特别是8CB+CH体系中从二级相变到一级相变的转变。