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首页> 外文期刊>Fluid Phase Equilibria >AN ENTHALPY-BASED CUBIC EQUATION OF STATE MIXING RULE FOR CROSS-PREDICTION OF EXCESS THERMODYNAMIC PROPERTIES OF HYDROCARBON AND HALOGENATED REFRIGERANT MIXTURES
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AN ENTHALPY-BASED CUBIC EQUATION OF STATE MIXING RULE FOR CROSS-PREDICTION OF EXCESS THERMODYNAMIC PROPERTIES OF HYDROCARBON AND HALOGENATED REFRIGERANT MIXTURES

机译:基于焓的立方混合状态方程式,用于交叉预测碳氢化合物和卤化制冷剂混合物的超热力学性质

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摘要

Mixing rules based on excess enthalpy of a binary fluid mixture were derived for Soave's equation. Specifically, the mixture SRK equation was cast in a form with complete separation of equation of state constants from thermodynamic variables P, V, and T yielding an equation of state with two volume parameters and one energy-volume parameter. An expression for the binary excess enthalpy was obtained, and the infinite-pressure limit was determined to provide a composition and temperature explicit expression for the SRK parameter a(M); a conventional linear mixing rule was used for b(M). This set of mixing rules was used with published excess enthalpy data to predict VLE for eleven binary systems comprised of simple aliphatic and halogenated hydrocarbons. A systematic analysis of the results by type of system shows the new mixing rule to be marginally superior to the original Soave polynomial mixing rules with k(12) = 0 or to an athermal form of the new mixing rule for a(M) (H-E = 0) for simple hydrocarbon systems. However, a marked improvement was observed for nonideal mixtures containing halogenated compounds for which conventional mixing rules with k(12) = 0 for the liquid phase generally fail. Moreover, when only a few excess enthalpy data for the single liquid phase (or supercritical fluid region) which could be fit to a simple polynomial expansion were available, excellent predictions were usually observed. Finally, the new mixing rules produce an approximately quadratic composition dependence of the vapor mixture second virial coefficient at low pressure as is required by statistical mechanics. [References: 64]
机译:为Soave方程推导了基于二元流体混合物的过量焓的混合规则。具体而言,将混合物SRK方程转换为状态常数方程与热力学变量P,V和T完全分离的形式,从而生成具有两个体积参数和一个能量体积参数的状态方程。获得了二元过量焓的表达式,并确定了无限大压力极限,以提供SRK参数a(M)的成分和温度显式表达式。 b(M)使用常规线性混合规则。这组混合规则与已发布的过量焓数据一起用于预测由简单的脂族和卤代烃组成的十一个二元系统的VLE。对按系统类型划分的结果进行系统分析表明,新混合规则在k(12)= 0时比原始Soave多项式混合规则略胜一筹,或者在a(M)(HE = 0)对于简单的碳氢化合物系统。但是,对于含卤代化合物的非理想混合物,观察到明显改善,对于这些混合物,传统的液相k(12)= 0混合规则通常无效。此外,当只有少量液相(或超临界流体区域)的过量焓数据可以拟合简单的多项式展开式时,通常会观察到极好的预测。最后,新的混合规则根据统计力学的要求,在低压下产生了蒸气混合物第二维里系数的近似平方组成依赖性。 [参考:64]

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