Thermodynamics of Mixtures Containing Oxaalkanes. 4. Random Mixing and Orientational Effects in Ether plus Alkane Systems

被引:17
作者
Antonio Gonzalez, Juan [1 ]
机构
[1] Univ Valladolid, Fac Ciencias, Dept Fis Aplicada, GETEF, Valladolid 47071, Spain
关键词
QUANTUM-MECHANICS CALCULATIONS; STRONGLY NEGATIVE DEVIATIONS; EXCESS MOLAR ENTHALPIES; KIRKWOOD-BUFF INTEGRALS; VAPOR-LIQUID-EQUILIBRIA; CHAIN MOLECULE LIQUIDS; PRIGOGINE-FLORY THEORY; BINARY-MIXTURES; HEAT-CAPACITIES; N-ALKANE;
D O I
10.1021/ie101264p
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Molar excess enthalpies, H-m(E), and volumes, V-m(E), of linear or cyclic ether + n-alkane systems have been discussed in terms of the effective dipole moment, (mu) over bar, of the ether, differences of standard enthalpies of vaporization of the ether and of the isomeric alkane, the number and relative positions of the oxygen atoms, the shape of the ether, and the relative size of the mixture compounds. The mentioned solutions have also been studied using the Flory model and the Kirkwood-Buff formalism. Both theories provide consistent results. At 298.15 K, the random mixing hypothesis is a good approximation for mixtures including linear or cyclic monoethers or linear diethers. Orientational effects become stronger in solutions with 2,5,8-trioxanonane, 2,5,8,11-tetraoxadodecane, or 2,5,8,1 1,14-pentaoxapentadecane. In the case of 1,3-dioxolane mixtures, this type of effect is more relevant than in systems with 1,4-dioxane. This is supported by W-shaped C-p,m(E) curves, large variations of the Flory interaction parameter, X-12, with the oxaalkane concentration, and local mole fractions of the ether-ether type that are higher than the bulk ones, particularly at lower x(1) values. The latter means that orientational effects are more important at this condition, and this is confirmed by large X-12 variations with x(1) in the region of low x(1) values. At equimolar composition. X-12 values of solutions containing 2,5,8,11-tetraoxadodecane or cyclic ethers remain nearly constant with the number of C atoms of the alkane, which reveals that systems with such oxaalkanes are similar from an interactional point of view. From values of the internal excess energies at constant volume, U-Vm(E), it is shown that interactions between like molecules are usually overestimated. Nevertheless, the general trends observed are independent of the H-m(E) or U-Vm(E) data considered. Structural effects are present in mixtures with components that differ largely in size (e.g., dipropyl ether + hexadecane or 2,5,8,11,14-pentaoxapentadecane + hexane).
引用
收藏
页码:9511 / 9524
页数:14
相关论文
共 122 条
[1]   THERMODYNAMIC PROPERTIES OF MIXTURES OF SMALL NONPOLAR MOLECULES [J].
ABE, A ;
FLORY, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1965, 87 (09) :1838-&
[2]  
ACREE WE, 1992, INT DATA SER SEL D A, V1, P50
[3]   CORRELATION OF THE PRIGOGINE-FLORY THEORY WITH ISOTHERMAL COMPRESSIBILITY AND EXCESS ENTHALPY DATA FOR BENZENE + NORMAL-ALKANE MIXTURES [J].
AICART, E ;
MENDUINA, C ;
ARENOSA, RL ;
TARADAJOS, G .
JOURNAL OF SOLUTION CHEMISTRY, 1983, 12 (10) :703-716
[4]   CORRELATION OF THE PRIGOGINE-FLORY THEORY WITH ISOTHERMAL COMPRESSIBILITY AND EXCESS ENTHALPY DATA FOR CYCLOHEXANE + ALKANE MIXTURES [J].
AICART, E ;
MENDUINA, C ;
ARENOSA, RL ;
TARDAJOS, G .
JOURNAL OF SOLUTION CHEMISTRY, 1984, 13 (06) :443-455
[5]   THERMODYNAMICS OF OLIGOMERIC BINARY-MIXTURES OF POLYETHYLENE-GLYCOL AND POLYPROPYLENE GLYCOL METHYLETHERS [J].
ALLEN, G ;
CHAI, Z ;
CHONG, CL ;
HIGGINS, JS ;
TRIPATHI, J .
POLYMER, 1984, 25 (02) :239-244
[6]   THERMODYNAMIC PROPERTIES OF CYCLOPENTANOL + PARA-DIOXANE MIXTURES AT 25 DEGREES C [J].
ANAND, SC ;
GROLIER, JPF ;
KIYOHARA, O ;
BENSON, GC .
CANADIAN JOURNAL OF CHEMISTRY, 1973, 51 (24) :4140-4144
[7]   Excess volumes of mixtures of glymes with normal, branched and cyclic alkanes [J].
Andreoli-Ball, L ;
Trejo, LM ;
Costas, M ;
Patterson, D .
FLUID PHASE EQUILIBRIA, 1998, 147 (1-2) :163-180
[8]   Thermodynamics of mixtures containing alkoxyethanols Part XXVII. Predictions on isobaric thermal expansion coefficients, compressibilities and speeds of sound from the Flory theory [J].
Antonio Gonzalez, Juan ;
Mozo, Ismael ;
Garcia De La Fuente, Isaias ;
Cobos, Jose Carlos ;
Riesco, Nicolas .
THERMOCHIMICA ACTA, 2008, 476 (1-2) :20-27
[9]   Application of the Flory Theory and of the Kirkwod-Buff Formalism to the Study of Orientational Effects in 1-Alkanol + Linear or Cyclic Monoether Mixtures [J].
Antonio Gonzalez, Juan ;
Riesco, Nicolas ;
Mozo, Ismael ;
Garcia De La Fuente, Isaias ;
Carlos Cobos, Jose .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2009, 48 (15) :7417-7429