Water Equilibrium in the Dehydration of Natural Gas With Triethylene Glycol

1973 ◽  
Vol 13 (05) ◽  
pp. 297-306 ◽  
Author(s):  
A. Rosman

Abstract To develop reliable design data for glycol contactors, gas-liquid equilibria in the system water-methane-triethylene glycol (TEG) were investigated experimentally. Equilibrium values vary little at the very high TEG concentrations used in modern contactor design, but increase significantly with increasing water concentration in the contacting TEG, and with increasing equilibrium temperature. Various methods of data correlation are described and compared with experimental data. The correlation provides the means for extending the results of this investigation to other pressures and temperatures. Introduction Water removal is a fundamental operation in natural gas processing. Hydrate formation, corrosion, and the formation of liquid water that might separate in the transmission lines are some of the problems caused by an excess of water in the gas. Of the methods available for gas dehydration, water absorption is by far the most generally used. Glycols, especially triethylene glycol (TEG), are the preferred absorbents. A survey of the literature on the water dew point of natural gas over glycol solutions reveals point of natural gas over glycol solutions reveals significant disagreements. A sampling of published dewpoint data for gas in equilibrium with TEG (Fig. 7) illustrates the prevailing confusion. Scant, but still contradictory, information was published for glycol concentrations in excess of 99.8 weight percent. Data in that range are needed in designing percent. Data in that range are needed in designing modern glycol contactors where the water dewpoint temperature must be reduced by more than 100 deg. F. The main reason for discrepancies in experimental results is the difficulty of measuring accurately very small amounts of water in gas. Water is easily adsorbed on the surfaces of experimental apparatus. Normally acceptable data scatter looms large in relation to the low water concentrations that must be measured. Attempts to establish water dew points on the basis of plant performance have been points on the basis of plant performance have been more successful. However, accuracy is limited by the difficulty in establishing the relative contribution of various factors that interrelate in plant operation. plant operation. Faced with these doubts, contactor designers have chosen to provide for TEG circulation rates that are overly high so as to insure more than adequate water removal. Such a practice is undesirable, however, where space and power are at a premium, as on offshore production platforms. Thus, the range of this investigation was governed by the need to extend equilibrium information to the contact temperatures and TEG concentrations necessary m optimize glycol contactors on offshore production platforms. production platforms. New procedures were developed for sampling and analyzing very small concentrations of water in gas and in TEG. To avoid experimental difficulties encountered by previous authors, equilibrium was reached and samples were taken under dynamic conditions. Experimental equilibrium results were smoothed and correlated by several methods. Thermodynamic equations were used to check on the internal consistency of data and to calculate equilibrium constants at conditions outside the range of the investigation itself. The White expression, fitted to the COFRC experimental data, adequately describes the results within the range of temperatures and concentrations studied. DEFINITIONS AND METHODS At water dewpoint temperature, the water contained in a natural gas reaches saturation. Part of that water will condense if the gas is brought to a lower temperature or to a higher pressure. Thus, the "dewpoint temperature" describes the water content of the gas. When dewpoint gas contacts TEG, the water content of the gas decreases. The lower water content corresponds to saturation water at a lower temperature; that is, the dew point will be lower. The initial dewpoint temperature is the contacting temperature. The temperature corresponding to the lowered water content is the equilibrium dewpoint temperature, and the difference between the two temperatures is the dewpoint depression. SPEJ P. 297

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Kenneth Kekpugile Dagde ◽  
Jackson Gunorubon Akpa

Models of an absorber for dehydration of natural gas using triethylene glycol are presented. The models were developed by applying the law of conservation of mass and energy to predict the variation of water content of gas and the temperature of the gas and liquid with time along the packing height. The models were integrated numerically using the finite divided difference scheme and incorporated into the MATLAB code. The results obtained agreed reasonably well with industrial plant data obtained from an SPDC TEG unit in Niger-Delta, Nigeria. Model prediction showed a percentage deviation of 8.65% for gas water content and 3.41% and 9.18% for exit temperature of gas and liquid, respectively.


2021 ◽  
Vol 651 (3) ◽  
pp. 032090
Author(s):  
Xiaomei Zou ◽  
Fengxia Huang ◽  
Liming Zhang ◽  
Tumeng Gele
Keyword(s):  

2016 ◽  
Author(s):  
V. J Aimikhe ◽  
O. F Joel ◽  
S. S Ikiensikimama ◽  
S Iyuke

2015 ◽  
Vol 1112 ◽  
pp. 550-554
Author(s):  
M. Zaki Mubarok ◽  
Christian Adi Kurniawan

At the present paper, a process of magnesia (MgO) synthesis from East Java dolomite through hydrochloride acid leaching, precipitation and calcination as well as characteristic of the product is discussed. Results of the experimental works show that the dissolution rate of magnesium and calcium from dolomite in hydrochloride acid solution was very rapid. Complete magnesium extraction was obtained by the leaching test with acid concentration of 1.5 molar, particle size distribution of -325#, solid-liquid ratio 1:20 (g/mL), stirring speed 200 rpm at room temperature after only 10 seconds. Precipitation of Mg(OH)2 by the addition of 20% (v/v) CaO slurry into pregnant leach solution resulted in 97.5% Mg precipitation after 1 minute. Solution pH must be maintained at a level of 10-10.5 by adjusting CaO addition in order to minimize calcium co-precipitation and to obtain high purity of Mg(OH)2 precipitate. Calcinations of Mg(OH)2 were performed at temperature range of 550-800°C in which 99% of crystal water removal took place after 5 minute at temperature of 800°C. Lower temperature requires longer time of crystalline water removal from Mg(OH)2. XRF analysis showed MgO purity of 88% with the main impurities of calcium and chloride. XRD analysis detected the presences of calcium as calcite (CaCO3) and portlandite (Ca(OH)2) as impurities in the MgO product. SEM analysis of the MgO powder revealed a nano size of MgO with particle diameter of about 50 nm.


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