Correlations for Hydrocarbon Gas Viscosity and Gas Density - Validation and Correlation of Behavior Using a Large-Scale Database

2005 ◽  
Vol 8 (06) ◽  
pp. 561-572 ◽  
Author(s):  
Fabio E. Londono ◽  
Rosalind A. Archer ◽  
Thomas A. Blasingame

Summary The focus of this work is on the behavior of hydrocarbon-gas viscosity and gas density. The viscosity of hydrocarbon gases is a function of pressure, temperature, density, and molecular weight, while the gas density is a function of pressure, temperature, and molecular weight. This work presents new approaches for the prediction of gas viscosity and gas density for hydrocarbon gases over practical ranges of pressure, temperature, and composition. These correlations can be used for any hydrocarbon-gas production or transportation operations. In this work, we created a large database of measured gas viscosity and gas density. This database was used to evaluate existing models for gas viscosity and gas density. We also provide new models for gas density and gas viscosity, as well as optimization of existing models, using our new database. The objectives of this research are as follows:• To create a large-scale database of measured gas-viscosity and gas-density data. This database will contain all the information necessary to establish the applicability of various models for gas density and gas viscosity over a widerange of pressures and temperatures.• To evaluate a number of existing models for gas viscosity and gas density.• To develop new models for gas viscosity and gas density using our research database; these models are proposed and validated. For this study, we created a large database from existing sources available in the literature. The properties in our database include composition, viscosity, density, temperature, pressure, pseudo reduced properties, and the gas compressibility factor. We use this database to evaluate the applicability of existing models used to determine hydrocarbon-gas viscosity and hydrocarbon-gas density (or, more specifically, the gas z-factor). Finally, we developed new models and calculation approaches to estimate the hydrocarbon-gas viscosity, and we also provide an optimization of the existing equations of state (EOS) typically used for for the calculation of the gas z-factor. Introduction Hydrocarbon-Gas Viscosity. NIST—SUPERTRAP Algorithm. The state-of-the-art mechanism for the estimation of gas viscosity is most likely the computer program SUPERTRAP, developed at the U.S. Natl. Inst. of Standard sand Technology (NIST). SUPERTRAP was developed from pure-component and mixture data and is stated to provide estimates within engineering accuracy from the triple point of a given substance to temperatures of 1,340.33°F and pressures of 44,100 psia. Because the SUPERTRAP algorithm requires the composition for a particular sample, it generally would not be suitable for applications in which only the mixture gas gravity and compositions of any contaminants are known. Carr et al. Correlation. Carr et al. developed a two-step procedure to estimate hydrocarbon-gas viscosity. The first step is to determine the gas viscosity at atmospheric conditions (i.e., a reference condition). Once estimated, the viscosity at atmospheric pressure is then adjusted to conditions at temperature and pressure using a second correlation. The gas viscosity can be estimated with graphical correlations or using equations derived from these figures. Jossi et al. Correlation. Jossi et al. developed a relationship for the viscosity of pure gases and gas mixtures; this correlation includes pure components such as argon, nitrogen, oxygen, carbon dioxide, sulfur dioxide, methane, ethane, propane, butane, and pentane. This "residualviscosity" relationship can be used to predict gas viscosity with the "reduced"density at a specific temperature and pressure, as well as the molecular weight. The critical properties of the gas (i.e., the critical temperature and critical pressure) are also required. Our presumption is that the Jossi et al. correlation (or at least a similar type of formulation) can be used for the prediction of viscosity for pure hydrocarbon gases and hydrocarbon-gas mixtures. We will note that this correlation is rarely used for hydrocarbon gases (other correlations are preferred); however, we will consider the formulation given by Jossi etal. as a potential model for the correlation of hydrocarbon-gas-viscosity behavior.

1985 ◽  
Vol 25 (06) ◽  
pp. 927-934 ◽  
Author(s):  
O. Glaso

Abstract This paper presents a generalized correlation for predicting the minimum miscibility pressure (MMP) required for predicting the minimum miscibility pressure (MMP) required for multicontact miscible displacement of reservoir fluids by hydrocarbon, CO2, or N2 gas. The equations are derived from graphical correlations given by Benham et al. and give MMP as a function of reservoir temperature, C7+ molecular weight of the oil, mole percent methane in the injection gas, and the molecular weight of the intermediates (C2 through C6) in the gas. CO2 and N2 are represented in the current correlation by "equivalent" methane/propane- and methane/ethane-mixture injection gases, respectively. The study shows that for hydrocarbon systems, paraffinicity has an effect on MMP. In the equations, the C7+ paraffinicity has an effect on MMP. In the equations, the C7+ molecular weight of the oil is corrected to a K factor of 11.95, thereby accounting for varying paraffinicity. An additional temperature effect on N2 MMP is related to the API gravity of the oil. The N2 correlation, however, is not tested against measured MMP data other than those used to develop the equation and should be used with care. A correlation that accounts for the additional effect on CO2 MMP caused by the presence of intermediate components in the reservoir oil is presented. Predicted MMP's from the correlations developed are compared to experimental slim-tube displacement data from the literature and from our displacement tests on North Sea gas/oil systems. These displacement tests have been performed with a packed slim tube, where the effect of viscous fingering is reduced to a minimum. Introduction Multicontact miscibility is represented most easily with a ternary diagram, where the composition of the driving or displaced fluid is altered. This is obtained by vaporization of light hydrocarbon components into a driving gas or by condensation of hydrocarbon components from a driving gas into the reservoir oil. Miscibility between reservoir oils and hydrocarbon gases is achieved either by vaporization or by condensing-gas-drive mechanism, depending on the reservoir oil and injection-gas composition. With N2 and CO2, miscibility is obtained by vaporization, but with CO2, miscibility usually is achieved at lower pressure because CO2 extracts much higher-molecular-weight hydrocarbons from the reservoir oil than N2 gas. The prediction of miscibility conditions from ternary diagrams is based on experimentally determined or calculated gas and liquid compositions of a reservoir-oil/injection-gas mixture. The experimental gas and liquid equilibrium data are not easy to obtain and are often time-consuming to determine, especially near the plait point. The method for calculating gas and liquid data with point. The method for calculating gas and liquid data with equations of state to predict miscibility relies largely on gas and liquid compositions near the plait-point region. It is generally accepted that such data may not be sufficiently accurate. Flow experiments offer the most reliable method to determine the pressure required for miscibility with CO2, N 2, and hydrocarbon gas. The slim-tube method has been most widely used to determine miscibility. Different experimental procedures and interpretation criteria, however, have ted to different definitions of miscibility and have caused considerable confusion. The limitation of the slim-tube test and the problems associated with miscible displacement in porous media have been described by several authors. Phase behavior and mechanisms of miscible flooding with CO2, N2, and hydrocarbon gas have also been described by several authors. Correlations for predicting MMP have been proposed by a number of investigators and are important tools in the selection of potential reservoirs for gas miscible flooding. Therefore, the correlations must be as accurate as possible. Several CO2 MMP correlations have been published, but none of these can be used with enough published, but none of these can be used with enough confidence for final project design. They are useful, however, for screening and preliminary work. Correlations on CO2 miscible flooding have shown temperature to be the most important parameter but they disagree regarding the effect of oil type (e.g., C7+ properties of the oil). Compared with CO2 miscible flooding, very little has been published on high-pressure hydrocarbon gas miscible flooding. A recent publication gives a correlation for predicting MMP with lean hydrocarbon gases and nitrogen. In 1960, Benham et al. presented empirical curves that can estimate miscibility conditions for reservoir oils that are displaced by rich gas within a pressure range of 1,500 to 3,000 psia [10.34 to 20.68 MPa]. They assumed a limiting tie line (at the critical composition on a ternary diagram) parallel to the C1–C7+ axis and estimated mole percent methane in the injection gas from calculated percent methane in the injection gas from calculated critical points with pressure, temperature, molecular weights of C2 through C4 in the gas, and the C5+ molecular weight of the oil as variables. From Benham et al.'s data, the proposed equations have been derived for predicting MMP. SPEJ P. 927


2011 ◽  
Vol 66 (2) ◽  
pp. 76-81 ◽  
Author(s):  
H. Pedersen ◽  
T. L. Christiansen ◽  
M. A. J. Somers
Keyword(s):  

Catalysts ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 757
Author(s):  
Huiyi Shang ◽  
Danni Yang ◽  
Dairong Qiao ◽  
Hui Xu ◽  
Yi Cao

Levan has wide applications in chemical, cosmetic, pharmaceutical and food industries. The free levansucrase is usually used in the biosynthesis of levan, but the poor reusability and low stability of free levansucrase have limited its large-scale use. To address this problem, the surface-displayed levansucrase in Saccharomyces cerevisiae were generated and evaluated in this study. The levansucrase from Zymomonas mobilis was displayed on the cell surface of Saccharomyces cerevisiae EBY100 using a various yeast surface display platform. The N-terminal fusion partner is based on a-agglutinin, and the C-terminal one is Flo1p. The yield of levan produced by these two whole-cell biocatalysts reaches 26 g/L and 34 g/L in 24 h, respectively. Meanwhile, the stability of the surface-displayed levansucrases is significantly enhanced. After six reuses, these two biocatalysts retained over 50% and 60% of their initial activities, respectively. Furthermore, the molecular weight and polydispersity test of the products suggested that the whole-cell biocatalyst of levansucrase displayed by Flo1p has more potentials in the production of levan with low molecular weight which is critical in certain applications. In conclusion, our method not only enable the possibility to reuse the enzyme, but also improves the stability of the enzyme.


Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 295
Author(s):  
Stephanie E. Doyle ◽  
Lauren Henry ◽  
Ellen McGennisken ◽  
Carmine Onofrillo ◽  
Claudia Di Bella ◽  
...  

Degradable bone implants are designed to foster the complete regeneration of natural tissue after large-scale loss trauma. Polycaprolactone (PCL) and hydroxyapatite (HA) composites are promising scaffold materials with superior mechanical and osteoinductive properties compared to the single materials. However, producing three-dimensional (3D) structures with high HA content as well as tuneable degradability remains a challenge. To address this issue and create homogeneously distributed PCL-nanoHA (nHA) scaffolds with tuneable degradation rates through both PCL molecular weight and nHA concentration, we conducted a detailed characterisation and comparison of a range of PCL-nHA composites across three molecular weight PCLs (14, 45, and 80 kDa) and with nHA content up to 30% w/w. In general, the addition of nHA results in an increase of viscosity for the PCL-nHA composites but has little effect on their compressive modulus. Importantly, we observe that the addition of nHA increases the rate of degradation compared to PCL alone. We show that the 45 and 80 kDa PCL-nHA groups can be fabricated via indirect 3D printing and have homogenously distributed nHA even after fabrication. Finally, the cytocompatibility of the composite materials is evaluated for the 45 and 80 kDa groups, with the results showing no significant change in cell number compared to the control. In conclusion, our analyses unveil several features that are crucial for processing the composite material into a tissue engineered implant.


Author(s):  
Makoto Ogata

Abstract Carbohydrates play important and diverse roles in the fundamental processes of life. We have established a method for accurately and a large scale synthesis of functional carbohydrates with diverse properties using a unique enzymatic method. Furthermore, various artificial glycan-conjugated molecules have been developed by adding these synthetic carbohydrates to macromolecules and to middle and low molecular weight molecules with different properties. These glycan-conjugated molecules have biological activities comparable to or higher than those of natural compounds, and present unique functions. In this review, several synthetic glycan-conjugated molecules are taken as examples to show design, synthesis and function.


2012 ◽  
Vol 12 (5) ◽  
pp. 628-636 ◽  
Author(s):  
Zuzana Kadlecova ◽  
Sophie Nallet ◽  
David L. Hacker ◽  
Lucia Baldi ◽  
Harm-Anton Klok ◽  
...  

1977 ◽  
Vol 30 (12) ◽  
pp. 2583 ◽  
Author(s):  
CP Hicks ◽  
CL Young

A technique for calculating the composition of two coexisting phases in equilibrium at a given temperature and pressure is described. The method is applicable, in principle, to any one-fluid model and any two- parameter closed equation of state. The philosophy of the technique is similar to that used in previous work on critical points.��� Values of (∂G/∂x2)T,P are calculated for mole fraction compositions ranging from zero to unity in small steps in order to locate (∂G/∂x2)T,P loops. Around each loop there is a region of phase separation and the compositions of coexisting phases are found by the usual equal-area line technique. ��� The use of the method is briefly illustrated by comparison with the experimental results for simple gas mixtures. The agreement between theory and experiment is satisfactory.


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