Casalini Riccardo, Paluch Marian, Roland C Michael
Chemistry Division, Code 6120, Naval Research Laboratory, Washington, DC 20375-5342, USA.
Phys Rev E Stat Nonlin Soft Matter Phys. 2003 Mar;67(3 Pt 1):031505. doi: 10.1103/PhysRevE.67.031505. Epub 2003 Mar 25.
Dielectric spectroscopy was carried out on the van der Waals liquid, 1,1(')-di(4-methoxy-5-methylphenyl)cyclohexane (BMMPC) in the supercooled state at pressures up to 218 MPa. The excess wing in this type-A glass former exhibits a response to pressure and temperature changes that is identical to that of the primary structural relaxation peak, indicating that the two processes reflect correlated molecular motions. Under no conditions was a distinct secondary peak observed in BMMPC, unlike the structurally very similar BMPC [1,1(')-bis(p-methoxyphenyl)cyclohexane]. However, the pressure dependences of both the glass temperature and fragility for the two materials are very close. The fragility is a decreasing function of pressure, although there is no concomitant narrowing of the relaxation peak. The pressure dependence of the relaxation times could be described as a simple volume-activated process, with the activation volume at the glass transition having the same magnitude as the molar volume.
在高达218兆帕的压力下,对处于过冷状态的范德华液体1,1(')-二(4-甲氧基-5-甲基苯基)环己烷(BMMPC)进行了介电谱研究。这种A型玻璃形成体中的过剩翼对压力和温度变化的响应与主要结构弛豫峰的响应相同,这表明这两个过程反映了相关的分子运动。与结构非常相似的BMPC [1,1(')-双(对甲氧基苯基)环己烷]不同,在任何条件下BMMPC中都未观察到明显的次级峰。然而,这两种材料的玻璃化温度和脆性的压力依赖性非常接近。脆性是压力的递减函数,尽管弛豫峰没有随之变窄。弛豫时间的压力依赖性可以描述为一个简单的体积激活过程,玻璃化转变时的激活体积与摩尔体积大小相同。