{"id":3041,"date":"2022-08-03T14:25:14","date_gmt":"2022-08-03T19:25:14","guid":{"rendered":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/?p=3041"},"modified":"2025-03-10T11:49:50","modified_gmt":"2025-03-10T16:49:50","slug":"https-petroskills-com-en-blog-entry-august2022-totm","status":"publish","type":"post","link":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/2022\/08\/https-petroskills-com-en-blog-entry-august2022-totm\/","title":{"rendered":"Part-2: Estimation of Solubilities of Benzene, Toluene and Ethylbenzene into Acid Gas Loaded Aqueous MDEA Solutions"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">In the Part &#8211; 1, July Tip of the month (TOTM), [1], the following items were discussed briefly:<\/p>\n\n\n\n<ul class=\"wp-block-list\"><li>Benzene, toluene, ethylbenzene, and xylene are members of the aromatics hydrocarbon family group, often referred to as BTEX. These aromatic compounds are also belonged to the broader category of Hazardous Air Pollutants (HAPs) [2]. BTEX can be present in many natural gas streams and are partially absorbed by the solvent in glycol dehydration and amine (e.g., MDEA) sweetening units. It is of specific interest to note that the components: Benzene, and Ethylbenzene are known carcinogens, thus substantiating their removal be solubility techniques.<\/li><li>&nbsp;In gas treating service, methyl diethanolamine (MDEA) will absorb limited quantities of BTEX from the gas. Based on literature data, predicted absorption levels for BTEX components vary from 5 to 30% [3]. Absorption is favored at lower temperatures, higher MDEA concentrations and circulation rates for normal operating Plant Unit Pressures 800 \u20131200 psia (56 \u2013 84 bar). The bulk of absorbed BTEX is separated from the MDEA in the regeneration unit and leaves the system in the regenerator overhead stream which requires further treatment before being vented to atmosphere.&nbsp; The amount of absorption of the BTEX is required to be known to determine the proper treating method for the overhead acid gases leaving the regenerator.<\/li><li>Correctly estimating the quantity of absorbed BTEX and understanding the factors that affect absorption levels is critical to ensure the proper mitigation methods are provided to meet the required emission limits.<\/li><li>The GPA Midstream research report RR-242 [4], is an extension of several previous GPA Midstream research projects looking at the solubility of hydrocarbons in loaded and unloaded amine solutions.&nbsp; The previous research included research reports RR-180, 185, 195, and RR-220.<\/li><li>Accurate hydrocarbon solubility data of RR-242 enables the development of new equation of state correlations that can be applied to the simulation of amine units (Bullin and Brown [3, 5]). The data can be used to optimize the design and operation of amine units in which these hydrocarbons are present in the feed gas. The data will provide a basis for accurately predicting the distribution of the heavier hydrocarbons between the treated gas, the amine flash gas, and the acid gas streams. The data will provide a basis for accurately predicting emissions of these hydrocarbons from the amine unit to aid in the design and operation of these units (Moshfeghian and Hubbard [6]).<\/li><\/ul>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a>Part \u2013 1 demonstrated applications of the models developed based on the experimental Vapor- Liquid Equilibrium (VLE) and Vapor-Liquid-Liquid Equilibrium (VLLE) data data measurements presented in RR-242 [3]. The models can be used for estimation of solubilities of selected hydrocarbons in pure water, unloaded amine solution, loaded amine solution with CO<sub>2<\/sub>\u00a0and\/or H<sub>2<\/sub>S.<\/a><\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1663__auto_fccf2acc643a237e6b70c24f34f42d8f\/1.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">Figure 1- Process flow diagram of MDEA acid gas recovery unit [3]<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a>This tip will focus on the following design variables:<\/a><\/p>\n\n\n\n<ul class=\"wp-block-list\"><li>Solubility of selected hydrocarbons in pure water, Equation 1, and Figure 2.<\/li><li>GPA Midstream RR-242 Proposed Model<\/li><li>Relative solubility of benzene, toluene, and ethylbenzene (EBenzene), Figure 3.<\/li><li>Solubility of benzene, toluene, and EBenzene in 50 wt % MDEA solution, Figure 4, and Table 2.<\/li><li>Multicomponent Hydrocarbons Phase<\/li><\/ul>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Solubility of Selected Hydrocarbons in Pure Water:<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Solubility of selected hydrocarbons in pure water can be estimated using Equation 1 [4] or Figure 2.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/2.png?ssl=1\">&nbsp; &nbsp;(1)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Where T is the temperature in K and the correlation parameters, E, F and T<sub>min<\/sub>, are shown in Table 1.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Table 1- Equation 1 parameters, E, F and T<sub>min<\/sub>&nbsp;[3].<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1666__auto_fccf2acc643a237e6b70c24f34f42d8f\/3.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">Figure 2 was generated using Equation 1 and its parameters in Table 1. The solubility of these selected hydrocarbons in pure water will be used to estimate their solubilities in amine solution in the proceeding sections.<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1667__auto_fccf2acc643a237e6b70c24f34f42d8f\/4.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">Figure 2. Solubility of selected hydrocarbons in pure water [4].<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Estimation\u00a0of solubility of hydrocarbons in amine solution by the GPA Midstream RR-242 Model [4]<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Equation 2 with its corresponding parameters will be used to estimate the solubility of selected hydrocarbons in unloaded and loaded amine solutions.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/5.png?ssl=1\">&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; (2)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Where:<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1665__auto_fccf2acc643a237e6b70c24f34f42d8f\/6.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">For simplicity and easiness of reading the figures, using the model (Equation 2) similar charts like Figures 3 and 4 or Table 2 were generated in Part \u2013 1 [1].<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1669__auto_fccf2acc643a237e6b70c24f34f42d8f\/7.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong><em>Figure 3 &#8211; Relative solubility of benzene (Fig 3), toluene (Fig 4), and Ethylbenzene (Fig 5) in loaded 50 wt % (13.1 mol-%) MDEA-Water [1]<\/em><\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a><strong>Convert 50 wt% MDEA to mole % MDEA<\/strong><\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Basis 100 kg of MDEA solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Mass of MDEA = 50 kg&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; MW of MDEA = 119.17 kg\/kmol<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Mass of water = 50 kg&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; MW of water = 18 kg\/kmol<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/8.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1670__auto_fccf2acc643a237e6b70c24f34f42d8f\/9.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1671__auto_fccf2acc643a237e6b70c24f34f42d8f\/10.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">Figure 4 &#8211; Solubility of benzene, toluene, and ethyl benzene in unloaded 50 wt % MDEA solution [1]<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Table 2 \u2013 Solubility (x0) of benzene, toluene, and ethylbenzene in unloaded 50 wt % MDEA solution [1]<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/11.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Example 1\u2013 Single Component Hydrocarbon\u00a0<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">This example and its solution on solubility of a single-component benzene in loaded 13.1 mol% (50 wt%) MDEA in water solution were presented in part 1 and shown in Appendix A of this tip.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Multicomponent Hydrocarbons Phase:&nbsp;<\/strong>GPA RR 242 [4] has presented the solubility measurements using a hydrocarbon phase consisting of equimolar amounts of Benzene, Toluene and Ethylbenzene. The acid gas used was CO2. The results are presented in Table 5. To evaluate the accuracy of Eq 2&nbsp;<strong>GPA RR-242 Model [4],&nbsp;<\/strong>we estimated the solubility of Benzene, Toluene and Ethylbenzene into loaded MDEA (50 wt %) aqueous solution for the conditions listed in Table 5 &#8211; GPA RR 242. In addition, a step &#8211; by &#8211; step hand calculations are shown in Example 2, the yellow highlighted values are the corresponding measured values reported in the highlighted row of Table 5.<strong><\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong><em>Table 5 &#8211; Solubility of Benzene, Toluene and Ethylbenzene into loaded MDEA (50 mass-%) aqueous solution Sapphire Apparatus. Hydrocarbon phase consists of x<\/em><\/strong><strong><em>1<\/em><\/strong><strong><em>=0.3329, x<\/em><\/strong><strong><em>2<\/em><\/strong><strong><em>=0.3335, x<\/em><\/strong><strong><em>3<\/em><\/strong><strong><em>=0.3336&nbsp;<\/em><\/strong><strong><em>[Table 5-GPA RR 242]<\/em><\/strong><\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1673__auto_fccf2acc643a237e6b70c24f34f42d8f\/12.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">a is loading mol acid gas\/mol amine, T is temperature, P is Pressure, \ud835\udc65\u0305 \u2013 average mole fraction, n &#8211; number of analyzed samples, \u03c3 &#8211; standard deviation<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Example 2 \u2013 Multicomponent Hydrocarbons Phase<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Determine the solubility of benzene, toluene, and ethylbenzene in loaded 13.1 mol% (50 wt%) MDEA in water solution in terms of scf of gas\/gal of solvent (std m<sup>3<\/sup>&nbsp;of gas\/m<sup>3<\/sup>&nbsp;of solvent) at 60 \u00b0C (140 \u00b0F), 333 K (600 \u00b0R).<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">The hydrocarbon phase consists of xB = 0.3329, xT = 0.3335, xEB = 0.3336. Rich amine solution acid gas loading,&nbsp;&nbsp;= 0.41 mol acid gases\/ mole MDEA, MDEA MW =119.17<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">50 wt % MDEA solution density =1017.3 kg\/m<sup>3<\/sup>&nbsp;(8.49 lbm\/gal)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">From Fig 3 presented in Part 1 (July 2022 TOTM), for&nbsp;&nbsp;= 0.41 mol acid gases\/ mole MDEA,<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">relative solubility solubilities are, (x\/x<sub>0<\/sub>)<sub>B<\/sub>&nbsp;= 0.52&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (x\/x<sub>0<\/sub>)<sub>T<\/sub>&nbsp;= 0.46&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (x\/x<sub>0<\/sub>)<sub>EB<\/sub>&nbsp;= 0.36<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">From Table 2 or Fig 4 presented in Part 1, for T =60 \u00b0C (140 \u00b0F),<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">the solubilities in unloaded MDEA are, (x<sub>0<\/sub>)<sub>B<\/sub>&nbsp;= 0.00464 &nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (x<sub>0<\/sub>)<sub>T<\/sub>&nbsp;= 0.00216&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (x<sub>0<\/sub>)<sub>EB<\/sub>&nbsp;= 0.00084<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Specified compositions (mole fractions) of hydrocarbon phase are, xB = 0.3329, xT = 0.3335, xEB = 0.3336<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1674__auto_fccf2acc643a237e6b70c24f34f42d8f\/13.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong><em>Figure 3 &#8211; Relative solubility of benzene (Fig 3), toluene (Fig 4), and Ethylbenzene (Fig 5) in loaded 50 wt % (13.1 mol-%) MDEA-Water<\/em><\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Table 2- Solubility of benzene, toluene, and ethyl benzene in unloaded 50 wt % MDEA solution<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/14.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><a><strong>Solution \u2013 SI<\/strong><\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Benzene:<\/strong>&nbsp;(x\/x<sub>0<\/sub>)<sub>B<\/sub>&nbsp;= 0.52&nbsp; (x<sub>0<\/sub>)<sub>B<\/sub>&nbsp;= 0.00464 &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xB = 1, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00464) (0.52) = 0.00242 kmol Ben\/kmol Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xB = 0.3329, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) (xB) = (0.00464) (0.52) (0.3329) = 0.0008 (vs. 0.00093) kmol Ben\/kmol Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">The yellow highlighted values are the measured values in Table 5<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">x = (0.0008 kmol Ben\/kmol Sol) (kmol Sol\/0.131kmol MDEA) =&nbsp;0.00611 kmol Ben\/kmol MDEA<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">\u00a0\u00a0 = (0.00611 kmol Ben\/kmol MDEA) (23.64 std m<sup>3<\/sup>\/kmol Ben) (kmol MDEA\/119.21 kg MDEA) =\u00a0\u00a0\u00a0 \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a00.0012 std m<sup>3<\/sup>\u00a0Ben\/kg of MDEA<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For each kg of MDEA we need 2 kg of sol (1 kg of MDEA + 1 kg of water)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">x = (0.0012 std m<sup>3<\/sup>&nbsp;Ben\/kg of MDEA) (kg MDEA\/2 kg Sol) (1017.3 kg Sol \/m<sup>3<\/sup>&nbsp;Sol)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp;&nbsp; = 0.62 std m<sup>3<\/sup>&nbsp;of Ben per m<sup>3<\/sup>&nbsp;of solution<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Or X = (770) [ (x<sub>0<\/sub>) (x\/x<sub>0<\/sub>) (xB)] std m<sup>3<\/sup>&nbsp;of Ben per m<sup>3<\/sup>&nbsp;of sol<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>X = (770) [0.0008] = 0.62 std m<sup>3<\/sup>&nbsp;of Ben per m<sup>3<\/sup>&nbsp;of solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>CF<\/strong>&nbsp;= (kmol Sol\/0.131kmol MDEA) (23.64 std m<sup>3<\/sup>&nbsp;Ben\/kmol Ben) (kmol MDEA\/119.21 kg MDEA)*<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (kg MDEA\/2 kg&nbsp; Sol) (1017.3 kg Sol \/m<sup>3<\/sup>&nbsp;Sol) = (770 std m<sup>3<\/sup>&nbsp;Ben\/m<sup>3<\/sup>&nbsp;Sol)(kmol Sol\/kmol Ben)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">The same color terms in the numerator and denominator cancel out.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>SI CF=&nbsp;<\/strong><strong>(770 std m<sup>3<\/sup>&nbsp;Ben\/m<sup>3<\/sup>&nbsp;Sol) (kmol Sol\/kmol Ben)<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Toluene:<\/strong>&nbsp;(x\/x<sub>0<\/sub>)<sub>T<\/sub>&nbsp;= 0.46&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (x<sub>0<\/sub>)<sub>T<\/sub>&nbsp;= 0.00216&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xT = 1, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00216) (0.46) = 0.00099 kmol Tol\/kmol MDEA Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xT = 0.3335, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00099) (0.3335) = 0.00033 vs. 0.00037 kmol Tol\/kmol Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>X = (770) [0.00033] = 0.26 std m<sup>3<\/sup>&nbsp;of Tol per m<sup>3<\/sup>&nbsp;of solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Ethylbenzene (EB)<\/strong>: (x\/x<sub>0<\/sub>)<sub>EB<\/sub>&nbsp;= 0.36&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (x<sub>0<\/sub>)<sub>EB<\/sub>&nbsp;= 0.00084<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xEB = 1, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00084) (0.36) = 0.00030 kmol EB\/kmol MDEA Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xEB = 0.3336, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00030) (0.3336) = 0.00010 vs. 0.000085 kmol EB\/kmol Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/strong><strong>X = (770) [0.00010] = 0.08 std m<sup>3<\/sup>&nbsp;of EB per m<sup>3<\/sup>&nbsp;of solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Solution &#8211; FPS<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Benzene:&nbsp;<\/strong>(x\/x<sub>0<\/sub>)<sub>B<\/sub>&nbsp;= 0.52&nbsp; (x<sub>0<\/sub>)<sub>B<\/sub>&nbsp;= 0.00464 &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xB = 1, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00464) (0.52) = 0.00242 lbmol Ben\/lbmol MDEA Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xB = 0.3329, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00464) (0.52) (0.3329) = 0.0008 (vs. 0.00093) lbmol Ben\/lbmol Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">The yellow highlighted values are the measured values in Table 5<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">x = (0.0008 lbmol Ben\/lbmol Sol) (lbmol Sol\/0.131lbmol MDEA) =&nbsp;0.00611 lbmol Ben\/lbmol MDEA<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;x = (0.00611 lbmol Ben\/lbmol MDEA) (379.5 scf\/lbmol Ben) (lbmol MDEA\/119.21 lbm)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;= 0.01945 scf Ben\/lbm of MDEA<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For each lbm of MDEA we need 2 lbm of sol (1 lbm of MDEA + 1 lbm of water)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;x = (0.01945 scf Ben\/lbm of MDEA) (lbm MDEA\/2 lbm Sol) (8.49 lbm\/gallon Sol)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp; &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;=&nbsp;0.083 scf of Ben\/gallon solution<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Or<\/strong>&nbsp;<strong>X = (103) [(x<sub>0<\/sub>) (x\/x<sub>0<\/sub>) (xB)] scf of Ben\/gallon of solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>X = (103) [0.0008] = 0.082 scf of Ben\/gallon of solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>CF<\/strong>&nbsp;= (lbmol Sol\/0.131lbmol MDEA) (379.5 scf Ben\/lbmol Ben) (lbmol MDEA\/119.21 lbm MDEA)*<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (lbm MDEA\/2 lbm Sol) (8.49 lbm Sol \/gallon Sol) = (103 scf Ben\/gallon Sol) (lbmol Sol\/lbmol Ben)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">The same color terms in the numerator and denominator cancel out.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>FPS CF&nbsp;<\/strong><strong>= (103 scf Ben\/gallon Sol) (lbmol Sol\/lbmol Ben)<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Toluene:<\/strong>&nbsp;(x\/x<sub>0<\/sub>)<sub>T<\/sub>&nbsp;= 0.46&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (x<sub>0<\/sub>)<sub>T<\/sub>&nbsp;= 0.00216&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xT = 1, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00216) (0.46) = 0.00099 kmol Tol\/kmol Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xT = 0.3335, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00099) (0.3335) = 0.00033 vs. 0.00037 kmol Tol\/kmol Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Or<\/strong>&nbsp;<strong>X = (FPS CF) [(x<sub>0<\/sub>) (x\/x<sub>0<\/sub>) (xT)] scf of Ben\/gallon of solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;<strong>X = (103) [0.00033] = 0.034 scf of Ben\/gallon of solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Ethylbenzene (EB):<\/strong>&nbsp;(x\/x<sub>0<\/sub>)<sub>EB<\/sub>&nbsp;= 0.36&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; (x<sub>0<\/sub>)<sub>EB<\/sub>&nbsp;= 0.00084<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xEB = 1, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00084) (0.36) = 0.00030 kmol EB\/kmol MDEA Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">For xEB = 0.3336, x= x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00030) (0.3336) = 0.00010 vs. 0.000085 kmol EB\/kmol Sol<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Or<\/strong>&nbsp;<strong>X = (103) [(x<sub>0<\/sub>) (x\/x<sub>0<\/sub>) (xEB)] scf of Ben\/gallon of solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>X = (103) [0.00010] = 0.010 scf of Ben\/gallon of solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">The estimated soluble BTE in the MDEA solution for example 2 and two other cases are compared with the measured values in Table 5R. This table indicates that the APD (absolute percent difference between the measured and estimated values) for eight out of nine estimated solubilities are less than 17.2. Considering very small amount of solubility, the Model estimation values are good facilities calculations and troubleshooting.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Table 5R \u2013 Measured and estimated solubility of Benzene, Toluene and Ethylbenzene into loaded MDEA (50 wt %) aqueous solution. Hydrocarbon phase consists of xB=0.3329, xT=0.3335, xEB=0.3336<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1677__auto_fccf2acc643a237e6b70c24f34f42d8f\/15.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\">APD = Absolute percent deviation =100*ABS (Exp Avg x \u2013 Model x) \/ (Exp Avg x)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Summary<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">From the RR-242 developed model based on the experimental results; several conclusions can be drawn.<\/p>\n\n\n\n<ul class=\"wp-block-list\"><li>Figures 3 and 4 or Table 2 present a simple tool for quick estimation of solubility of BETX compounds in 50 wt % MDEA gas treating process.<\/li><li>Figures 3 and 4 or Table 2 are suitable for 50 wt % (13.1 mol-%) MDEA in the MDEA-Water solution, similar chart and tables can generated for other different amines and concentrations.<\/li><li>For the examples considered in this tip and July TOTM, the estimated solubility for each of BETX compounds matched well with the experimental results.<\/li><\/ul>\n\n\n\n<p class=\"wp-block-paragraph\">To learn more about similar cases and how to minimize operational problems, we suggest attending our&nbsp;<a href=\"http:\/\/www.jmcampbell.com\/gas-conditioning-and-processing-g4.php\">G4 (Gas Conditioning and Processing)<\/a>,<strong><\/strong><a href=\"http:\/\/www.jmcampbell.com\/advanced-applications-in-gas-processing.php\">G5 (Advanced Applications in Gas Processing)<\/a><strong>,&nbsp;<\/strong><a href=\"http:\/\/www.jmcampbell.com\/co2-surface-facilities-pf81.php\">http:\/\/www.jmcampbell.com\/co2-surface-facilities-pf81.php<\/a>&nbsp;and<strong><\/strong><a href=\"http:\/\/www.jmcampbell.com\/oil-production-and-processing-facilities-pf4.php\"><u>PF49 (Troubleshooting Oil &amp; Gas Processing Facilities)<\/u>,<\/a><strong><\/strong>courses.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><em>By: Mahmood Moshfeghian, Ph.D.<\/em><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">References:<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">1.&nbsp;&nbsp;&nbsp;&nbsp; Moshfeghian, M. and Snow\u2013McGregor, K., www.petroskills.com\/en\/blog\/entry\/july2022-totm, PetroSkills July TOTM, 2022.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">2.&nbsp;&nbsp;&nbsp;&nbsp; &nbsp;http:\/\/www.earthworksaction.org\/BTEX.cfm, 2011.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">3.&nbsp;&nbsp;&nbsp;&nbsp; &nbsp; Campbell, J. M. \u201cGas conditioning and processing, Volume 2: The Equipment Modules,\u201d 9<sup>th<\/sup>&nbsp;Edition, 2<sup>nd<\/sup>&nbsp;Printing, Editors Hubbard, R. and Snow\u2013McGregor, K., Campbell Petroleum Series, Norman, Oklahoma, 2014.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">4.&nbsp;&nbsp;&nbsp;&nbsp; Uusi-Kyyny, P., Pakkanen, M., Richon, D., Ionita, S., Ogunrobo, E., Alopaeus, V., RR-242, \u201cSolubility of Hydrocarbons in Amine Treating Solutions\u201d, GPA Midstream Association, Tulsa, OK, 2019.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">5.&nbsp;&nbsp;&nbsp;&nbsp; Bullin, J. A., Brown, W.G., Hydrocarbons and BTEX Pickup and Control from Amine Systems\u201d, 83<sup>rd<\/sup>&nbsp;&nbsp;Gas Processors Association Annual Convention, Mar. 2004.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">6.&nbsp;&nbsp;&nbsp;&nbsp; Moshfeghian, M. and R.A. Hubbard, \u201cQuick Estimation of Absorption of Aromatics Compounds (BTEX) in TEG Dehydration Process\u201d, 3<sup>rd<\/sup>&nbsp;International Gas Processing Symposium, March 5-7, Doha, Qatar, 2012.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Appendix A<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Example 1<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Determine the solubility of benzene in loaded 13.1 mol% (50 wt%) MDEA in water solution in terms of scf of gas\/gal of solvent (std m<sup>3<\/sup>&nbsp;of gas\/m<sup>3<\/sup>&nbsp;of solvent) at 60 \u00b0C (140 \u00b0F), 333 K (600 \u00b0R).<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Rich amine solution acid gas loading,&nbsp;&nbsp;= 0.4 mol acid gases\/ mole MDEA, MDEA MW =119.17<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">50 wt % MDEA solution density =1017.3 kg\/m<sup>3<\/sup>&nbsp;(8.49 lbm\/gal)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">From Fig 1, for&nbsp;&nbsp;= 0.4 mol acid gases\/ mole MDEA, relative solubility, x\/x<sub>0<\/sub>= 0.53<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Benzene solubility in un-loaded MDEA, x<sub>0<\/sub>&nbsp;= 0.00464<\/p>\n\n\n\n<figure class=\"wp-block-image\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" src=\"https:\/\/i0.wp.com\/petroskills.com\/blog\/totm-graphs\/Aug2022\/image-thumb__1676__auto_fccf2acc643a237e6b70c24f34f42d8f\/16.png?ssl=1\" alt=\"\"\/><\/figure>\n\n\n\n<p class=\"wp-block-paragraph\"><strong><em>Figure 1 &#8211; Relative solubility of Benzene in 50 weight % (13.1 mol-%) MDEA-Water [Figure 16 of GPA RR 242].<\/em><\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Solution &#8211; SI<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">X = x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00464) (0.53kmol Ben\/kmol MDEA Sol) (kmol MDEA Sol\/0.131kmol MDEA)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp; = (0.0187 kmol Ben\/kmol MDEA) (23.64 std m<sup>3<\/sup>\/kmol Ben) (kmol MDEA\/119.21 kg)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp;&nbsp; = (0.0037 std m<sup>3<\/sup>&nbsp;Ben\/kg of MDEA) (kg MDEA\/2 kg MDEA + Water Sol) (1017.3 kg\/m<sup>3<\/sup>&nbsp;MDEA Sol)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp;&nbsp; = 1.88 std m<sup>3<\/sup>&nbsp;of Ben\/m<sup>3<\/sup>&nbsp;of MDEA + water solution<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Or<\/strong>&nbsp;<strong>X = (770) (x<sub>0<\/sub>) (x\/x<sub>0<\/sub>) std m<sup>3<\/sup>&nbsp;of Ben\/m<sup>3<\/sup>&nbsp;of MDEA + water solution<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Solution &#8211; FPS<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">X = x<sub>0<\/sub>(x\/x<sub>0<\/sub>) = (0.00464) (0.53 lbmol Ben\/lbmol MDEA Sol) (lbmol MDEA Sol\/0.131lbmol MDEA)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp; = (0.0187 lbmol Ben\/lbmol MDEA) (379.5 scf\/lbmol Ben) (lbmol MDEA\/119.21 lbm)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp;&nbsp; = (0.0598 scf Ben\/lbm of MDEA) (lbm MDEA\/2 lbm MDEA + Water Sol) (8.49 lbm\/gallon MDEA Sol)<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">&nbsp;&nbsp;&nbsp; = 0.25 scf of Ben\/gallon of MDEA + water solution<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Or<\/strong>&nbsp;<strong>X = (103) (x<sub>0<\/sub>) (x\/x<sub>0<\/sub>) scf of Ben\/gallon of MDEA + water solution<\/strong><\/p>\n","protected":false},"excerpt":{"rendered":"<p>In the Part &#8211; 1, July Tip of the month (TOTM), [1], the following items were discussed briefly: Benzene, toluene, ethylbenzene, and xylene are members of the aromatics hydrocarbon family group, often referred to as BTEX. These aromatic compounds are also belonged to the broader category of Hazardous Air Pollutants (HAPs) [2]. BTEX can be [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"nf_dc_page":"","_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_feature_clip_id":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":false,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"font":"","enabled":false},"version":2},"jetpack_post_was_ever_published":false},"categories":[1],"tags":[],"coauthors":[17],"class_list":["post-3041","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"jetpack_publicize_connections":[],"jetpack_featured_media_url":"","jetpack_shortlink":"https:\/\/wp.me\/p1pQc4-N3","jetpack_sharing_enabled":true,"_links":{"self":[{"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/posts\/3041","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/comments?post=3041"}],"version-history":[{"count":1,"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/posts\/3041\/revisions"}],"predecessor-version":[{"id":3042,"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/posts\/3041\/revisions\/3042"}],"wp:attachment":[{"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/media?parent=3041"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/categories?post=3041"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/tags?post=3041"},{"taxonomy":"author","embeddable":true,"href":"http:\/\/www.jmcampbell.com\/tip-of-the-month\/wp-json\/wp\/v2\/coauthors?post=3041"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}