Unidade de regeneração de monoetilenoglicol: dados experimentais e modelagem termodinâmica

Gas hydrates are crystalline solids and may cause several harsh consequences for natural gas production in subsea lines. Monoethylene glycol (MEG) is the most used thermodynamic hydrate inhibitor. Vapor–liquid equilibrium (VLE) data for aqueous systems in the presence of electrolytes have many indus...

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Autor principal: Monteiro, Mateus Fernandes
Outros Autores: Chiavone Filho, Osvaldo
Formato: Dissertação
Idioma:pt_BR
Publicado em: Universidade Federal do Rio Grande do Norte
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Endereço do item:https://repositorio.ufrn.br/handle/123456789/33321
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Resumo:Gas hydrates are crystalline solids and may cause several harsh consequences for natural gas production in subsea lines. Monoethylene glycol (MEG) is the most used thermodynamic hydrate inhibitor. Vapor–liquid equilibrium (VLE) data for aqueous systems in the presence of electrolytes have many industrial applications. VLE data for water + MEG mixtures in the presence of sodium chloride at low pressures are important to describe the effects of composition, temperature, and pressure on MEG regeneration unit. The regeneration aims to remove water and salt present in the rich MEG stream, resulting in lean MEG. In the gas production context, MEG is regenerated to reduce operational costs, due to the large amount required. The MEG regeneration process consists mainly of a three-phase separator, flash evaporator with brine removal, and distillation column. A modified version of the Othmer ebulliometer was applied to measure reliable VLE data for water + MEG + NaCl at 101.325, 65 and 35 kPa. Binary systems water + MEG and MEG + NaCl were also experimentally studied. The Electrolyte Non–random Two–Liquid (ENRTL) and Universal Quasi-Chemical Activity Coefficient (UNIQUAC) models were successfully parameterized to describe the VLE behavior for water + MEG+ NaCl systems. Thermodynamic consistence of the datasets was also checked. MEG+NaCl solutions presented an inverted colligative property, i.e., the addition of salt decreases the boiling point. NaCl solubility were also measured from 293.15 to 403.15 K in the whole MEG concentration range. The experimental method used for the determination of salt solubility data was analytical (density measurements) and based on the reproducibility of the concentration of two successive samples. The temperature dependence on the solubility of NaCl is relatively weak compared to other salts and a reverse trend behavior with increasing temperature has been described for MEG contents higher than 90 wt%. Excess solubility has been correlated with Redlich–Kister expansion. Solid–liquid equilibrium data were also used for ENRTL parametrization aiming the description of solid–liquid and vapor–liquid equilibrium with a unique set of parameters.