A predictive correlation for the constant-pressure specific heat capacity of pure and ill-defined liquid hydrocarbons

被引:30
作者
Dadgostar, Nafiseh [1 ]
Shaw, John M. [1 ]
机构
[1] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB T6G 2G6, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Heat capacity; Prediction; Hydrocarbons; Liquids; III-defined; Heteroatoms; Elemental analysis; Similarity variable; Lee-Kesler correlation; TEMPERATURE THERMODYNAMIC PROPERTIES; SOLID ORGANIC-COMPOUNDS; DEEP HYDRODESULFURIZATION; ENTHALPY INCREMENTS; POSSIBLE PRECURSORS; THERMAL-PROPERTIES; PHASE-BEHAVIOR; N-PROPYL; VAPORIZATION; EQUILIBRIA;
D O I
10.1016/j.fluid.2011.09.015
中图分类号
O414.1 [热力学];
学科分类号
摘要
A predictive correlation for the constant pressure specific liquid heat capacity (C-p) valid for pure organic compounds and ill-defined mixtures such as heavy oil and bitumen is reported. With six universal coefficients. the correlation is a function of temperature and a similarity variable, alpha, which is proportional to the number of atoms per unit mass. Molecule structure is shown to be a variable of secondary importance and only the elemental composition of a liquid is required to apply the correlation. A training data set comprising 150 experimental heat capacity values for 19 liquid organic compounds (including paraffins, naphthenes, aromatics, sulphur/oxygen/nitrogen derivatives) and 3 molten polymers in the temperature range (207-590) K was used to regress coefficients. The correlation was evaluated using a test data set comprising 111 heat capacity values for 12 liquid organic compounds and 3 molten polymers. The average absolute deviation for the test data set was found to be 0.067 J K-1 g(-1). The correlation appears to be preferred over the Lee-Kesler correlation, a common reference equation for engineering calculations, both with respect to over all accuracy, and range of application. The correlation was also applied to two ill-defined hydrocarbon liquids, namely Athabasca and Maya pentane maltenes. For such ill-defined hydrocarbon liquids neither molecular structure nor critical properties are available. Their liquid heat capacities were predicted to within 6.0 and 2.8%. respectively from 325 K to more than 500 K. This is the first such prediction, and represents a significant advance over prior practice. With this new predictive correlation, liquid phase heat capacities for ill-defined hydrocarbon fluids, such as bitumen, and pure compounds and polymers can be predicted with equal ease. The correlation may also be used for the development of high-accuracy fluid-specific correlations where warranted by customizing one or more of the universal coefficients. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:211 / 226
页数:16
相关论文
共 47 条
[21]  
Lee B.I., 1975, COMMUNICATION
[22]   GENERALIZED THERMODYNAMIC CORRELATION BASED ON 3-PARAMETER CORRESPONDING STATES [J].
LEE, BI ;
KESLER, MG .
AICHE JOURNAL, 1975, 21 (03) :510-527
[23]   THE LOW-TEMPERATURE THERMODYNAMIC PROPERTIES OF NAPHTHALENE, 1-METHYLNAPHTHALENE, 2-METHYLNAPHTHALENE, 1,2,3,4-TETRAHYDRONAPHTHALENE, TRANS-DECAHYDRONAPHTHALENE AND CIS-DECAHYDRONAPHTHALENE [J].
MCCULLOUGH, JP ;
FINKE, HL ;
MESSERLY, JF ;
TODD, SS ;
KINCHELOE, TC ;
WADDINGTON, G .
JOURNAL OF PHYSICAL CHEMISTRY, 1957, 61 (08) :1105-1116
[24]   LOW-TEMPERATURE THERMAL PROPERTIES OF 2-METHYLHEPTANE AND 2-METHYLDECANE - THERMODYNAMIC PROPERTIES OF 2-METHYLALKANES [J].
MESSERLY, JF ;
FINKE, HL .
JOURNAL OF CHEMICAL THERMODYNAMICS, 1971, 3 (05) :675-&
[25]   LOW-TEMPERATURE THERMODYNAMIC PROPERTIES OF N-PROPYL- N-BUTYL- AND N-DECYL-SUBSTITUTED CYCLOPENTANES [J].
MESSERLY, JF ;
TODD, SS ;
FINKE, HL .
JOURNAL OF PHYSICAL CHEMISTRY, 1965, 69 (02) :353-&
[26]   Thermal data on organic compounds. VI. The heat capacities, entropies and free energies of some saturated, non-benzenoid hydrocarbons [J].
Parks, GS ;
Huffman, HM ;
Thomas, SB .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1930, 52 :1032-1041
[27]   Thermodynamics of 1-alkanol plus n-alkane mixtures:: new data and predictions from the NTGC model [J].
Peleteiro, J ;
González-Salgado, D ;
Cerdeiriña, CA ;
Valencia, JL ;
Romaní, L .
FLUID PHASE EQUILIBRIA, 2001, 191 (1-2) :83-97
[28]   THE HEAT CAPACITY, HEATS OF FUSION AND VAPORIZATION, VAPOR PRESSURE, ENTROPY, VIBRATION FREQUENCIES AND BARRIER TO INTERNAL ROTATION OF STYRENE [J].
PITZER, KS ;
GUTTMAN, L ;
WESTRUM, EF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1946, 68 (11) :2209-2212
[29]  
Poling B., 2001, The Properties of Gases and Liquids, V5th, DOI DOI 10.1036/0070116822
[30]  
Poling B.E., 1987, PROPERTIES GASES LIQ, V5th