Mechanisms by Which Pentane and Hexane Adsorb on Silica Gel

1966 ◽  
Vol 6 (02) ◽  
pp. 166-174 ◽  
Author(s):  
H.O. McLeod ◽  
J.M. Campbell

Abstract Data analysis of pentane and hexane adsorption from natural gas in a fixed bed of silica gel shows that constant length mass transfer zones form, the curvature of the adsorption isotherm controls the growth of the mass transfer zone and surface diffusion of molecules inside the silica gel particle controls the mass transfer rate. Curvature of the hexane isotherm is more than the curvature of the pentane isotherm. Because of this curvature the hexane adsorption zones reached a constant length. In contrast, the pentane adsorption zones were always increasing in length during each run. A procedure was developed to obtain correct mass transfer coefficients using effluent curve slopes. These transfer coefficients increase with the amount of hydrocarbon adsorbed on the silica gel particle. The characteristic shape of the hexane effluent curves also show that molecular diffusion inside the silica gel particle controls the adsorption rate of pentane and hexane. Introduction The purpose of this study was to determine the mechanisms that control the dynamic adsorption of hydrocarbons from a natural gas onto silica gel. Before one can deal effectively with multicomponent adsorption, the transfer mechanisms by which a single hydrocarbon component is adsorbed from the gas stream must be defined. Two principal investigations of this system have been published and indicate that diffusion through the gas around the particle controls the adsorption rate. Some of the experimental observations in each study either do not support this transfer mechanism or are inconsistent with the mathematical model used in analysis. In this study surface diffusion of molecules inside the particle controls the mass transfer rate of pentane and hexane. This mechanism is indicated by the effluent curve shape for a constant length transfer zone and by the variation of the mass transfer coefficient with concentration of the adsorbed hydrocarbon. THEORY AND DEFINITIONS-MATHEMATICAL MODELS Mathematical solutions for the isothermal adsorption of a trace component from a carrier gas are derived from three relationships: the mass balance or continuity equation, the equilibrium relationship between the gas and solid phases, and a mass transfer rate equation. The transfer rate is proportional to the adsorbate concentration gradient within either the gas or solid phase. Mathematical solutions of these equations usually give the adsorbate concentration as a function of time and distance from the bed inlet. That part of the bed in which the adsorbate concentration changes from a maximum to a minimum value is called the transfer zone. This transfer zone is directly related to a plot of the effluent concentration vs time which has a characteristic S-shape. This general shape is determined by the continuity equation and occurs in many processes of diffusional transfer. EQUILIBRIUM ADSORPTION ISOTHERMS Different mathematical models of fixed bed adsorption occur mainly because different equilibrium adsorption isotherms are assumed. Eq. 1 describes the amount of hydrocarbon adsorbed as a function of the amount of hydrocarbon in the gas phase at a constant temperature: ........................................(1) There are two main models which describe the separation of a trace component in a fixed bed. Model A assumes a linear isotherm (r = 1); Model B assumes a favorably curved isotherm (r is less than 1). SPEJ P. 166ˆ

Processes ◽  
2021 ◽  
Vol 9 (7) ◽  
pp. 1169
Author(s):  
Kyle McGaughy ◽  
M. Toufiq Reza

Common solvents used for aromatic extraction from aliphatics typically degrade into toxic compounds, while green alternatives perform poorly compared to the state-of-the-art solvents. Deep eutectic solvents (DES) are a novel solvent type made of hydrogen bond donors (HBD) and hydrogen bond acceptors (HBA). DES have been applied in various applications, including advanced separations. In this study, DES were studied experimentally and using the Conductor-like Screening Model (COSMO) to separate benzene from cyclohexane as model compounds for an aromatic:aliphatic system. Both equilibrium and kinetic studies were performed to determine the liquid liquid equilibrium (LLE) and mass transfer rate for the DES-based separation. Selected HBAs including tetrabutylammonium bromide (N4444Br), tetrahexylammonium bromide (N6666Br), choline chloride (ChCl), and methyltriphenylphosphonium bromide (METPB) were paired with HBDs including ethylene glycol (EG) and glycerol (Gly). COSMO was used, with adjustments to reflect DES specific interactions, to predict the liquid-liquid equilibrium (LLE). COSMO results showed that ChCl and N6666Br-based DES extracted too little benzene or too much cyclohexane, respectively, to be considered for experimental evaluation. Overall, the COSMO model predictions for LLE of EG-based DES were very accurate, with root-mean-square deviations (RMSD) below 1% for both N4444Br:EG and METPB:EG. The glycerol systems were less accurately modeled, with RMSD’s of 4% for N4444Br:Gly and 6% for METPB:Gly. The lower accuracy of glycerol system predictions fmay be due to limitations in COSMO for handling glycerol’s influence on polarizability in the DES that is not seen in EG-based DES. Mass transfer kinetics were determined experimentally for DES and the results were fit to a first order kinetics model. METPB:Gly had the highest mass transfer coefficient at 0.180 min−1, followed by N4444Br:EG at 0.143 min−1. N4444Br:Gly and METPB:EG had the lowest mass transfer coefficients at 0.096 min−1 and 0.084 min−1, respectively. It was found that mass transfer rate was not directly related to maximum benzene solubility, as N4444Br:EG and METPB:Gly had the highest and lowest benzene removal, respectively, but had similar mass transfer coefficients.


1997 ◽  
Vol 35 (7) ◽  
pp. 295-302 ◽  
Author(s):  
Ervin Orlandini ◽  
Tsegaye G. Gebereselassie ◽  
Joop C. Kruithof ◽  
Jan C. Schippers

Background Organic Matter (BOM) preloading is adsorption of BOM onto Granular Activated Carbon (GAC) prior to the adsorption of target compounds, such as pesticides and other organic micropollutants (e.g. atrazine). BOM preloading is commonly found to speed up the breakthrough of target compounds during GAC filtration. Ozonation of GAC filter influent may be expected to lower BOM preloading, because it results in less adsorbable and more biodegradable BOM compounds. Short Fixed Bed (SFB) tests with virgin and preloaded GAC, performed within this study, confirmed that preloading of BOM present in pretreated river Rhine water speeds up the breakthrough of atrazine in GAC filters. BOM preloading was found to lower equilibrium adsorption capacity of GAC for atrazine, and to slow down both external and internal mass transfer rate of atrazine on/into GAC. Adsorption capacity of (crushed) GAC was determined from atrazine adsorption isotherms, while mass transfer rate coefficients were determined by fitting the Homogeneous Surface Diffusion model to the breakthrough of atrazine in the SFB tests. More pronounced BOM preloading was found in the GAC filter receiving non-ozonated influent than in its ozonated counterpart. Biodegradation of ozonated BOM was shown to lower BOM preloading in GAC filters.


2003 ◽  
Vol 68 (11) ◽  
pp. 2080-2092 ◽  
Author(s):  
Martin Keppert ◽  
Josef Krýsa ◽  
Anthony A. Wragg

The limiting diffusion current technique was used for investigation of free convective mass transfer at down-pointing up-facing isosceles triangular surfaces of varying length and inclination. As the mass transfer process, copper deposition from acidified copper(II) sulfate solution was used. It was found that the mass transfer rate increases with inclination from the vertical to the horizontal position and decreases with length of inclined surface. Correlation equations for 7 angles from 0 to 90° were found. The exponent in the ShL-RaL correlation ranged from 0.247 for the vertical case, indicating laminar flow, to 0.32 for inclinations of 60 to 90°, indicating mixed or turbulent flow. The general correlation ShL = 0.358(RaL sin θ)0.30 for the RaL sin θ range from 7 × 106 to 2 × 1011 and inclination range from 15 to 90° was obtained.


2000 ◽  
Vol 55 (7) ◽  
pp. 1257-1267 ◽  
Author(s):  
Tiruta-Barna Ligia ◽  
Barna Radu ◽  
Moszkowicz Pierre ◽  
Bae Hae-Ryong

RSC Advances ◽  
2016 ◽  
Vol 6 (111) ◽  
pp. 109978-109982 ◽  
Author(s):  
Young-Kee Kim ◽  
Sung-Yeob Lee ◽  
Byung-Keun Oh

In an enzyme process using a gas substrate, the enhanced gas liquid mass transfer rate of the gas substrate by methyl-functionalized mesoporous nanoparticles could improve the productivity.


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