Measuring and Thermodynamic Modeling of De-Mixing CO2 ...€¦ · Waseem Arshad, Muhammad...
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Measuring and Thermodynamic Modeling of De-Mixing CO2 Capture Systems
Waseem Arshad, Muhammad
Publication date:2014
Document VersionPublisher's PDF, also known as Version of record
Link back to DTU Orbit
Citation (APA):Waseem Arshad, M. (2014). Measuring and Thermodynamic Modeling of De-Mixing CO2 Capture Systems.Technical University of Denmark, Department of Chemical and Biochemical Engineering.
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Muhammad Waseem ArshadPh.D. ThesisJune 2014
Measuring and Thermodynamic Modeling of De-Mixing CO2 Capture Systems
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Copyright©: Muhammad Waseem Arshad
June 2014
Address: Center for Energy Resources Engineering
Department of Chemical and
Biochemical Engineering
Technical University of Denmark
Søltofts Plads, Building 229
DK-2800 Kgs. Lyngby
Denmark
Phone: +45 4525 2800
Fax: +45 4525 4588
Web: www.cere.dtu.dk
Print: J&R Frydenberg A/S
København
December 2014
ISBN: 978-87-93054-55-4
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Freezing Point Depressions of Phase Change CO2 SolventsMuhammad Waseem Arshad, Philip Loldrup Fosbøl, Nicolas von Solms, and Kaj Thomsen*
Technical University of Denmark, Department of Chemical and Biochemical Engineering, Center for Energy Resources Engineering(CERE), Søltofts Plads Building 229, DK-2800 Kongens Lyngby, Denmark
ABSTRACT: Freezing point depressions (FPD) in phase change solventscontaining 2-(diethylamino)ethanol (DEEA) and 3-(methylamino)propylamine(MAPA) were measured using a modified Beckmann apparatus. Themeasurements were performed for the binary aqueous DEEA and MAPAsolutions, respectively, in the concentration ranges of (0 to 55) mass percentand (0 to 32.5) mass percent of amine. For the ternary aqueous DEEA−MAPAsolutions, freezing points were measured for 5:1, 3:1, 1:1, 1:3, and 1:5 molarratios of DEEA/MAPA. The FPD method was extended for easy and accuratemeasurement of freezing points in the CO2 loaded systems. It is based onsaturation of the solution by CO2 and then dilution by using a batch of theoriginal unloaded solution in order to get the solutions with different CO2loadings. Freezing point measurements were then carried out for (12, 20, 30, and 33) mass percent DEEA solutions and (10, 20,and 27) mass percent MAPA solutions at different CO2 loadings. The apparatus and the experimental method used showed goodrepeatability and accuracy. The measured freezing point data were compared with monoethanolamine (MEA) and methyldiethanolamine (MDEA) found in the literature. The experimental values indicate that the DEEA−water interaction is almostsimilar to that of MEA−water interaction. MAPA has shown a stronger nonideal behavior compared to DEEA. A correlation forthe freezing points as a function of solution composition was formulated for the unloaded binary and ternary systems.
1. INTRODUCTION
Reactive absorption using amines is one of the most commonindustrial technologies available today for the postcombustionCO2 capture. These processes have been considered as themost feasible route to capture CO2 from power plant flue gases.This is due to their use in many industrial applications, such asCO2 removal from reformer gases, acid gas removal fromnatural gas, etc.1 The amine based scrubbing selectivelyremoves CO2 from the flue gases and releases a high-purityCO2 offgas stream upon heating in a stripper column which issuitable for storage without any further treatment. However,the energy requirement for solvent regeneration is very high inthese processes.2,3 Therefore, the development of new solventsystems with improved energy efficiency, innovative processdesign, and technological improvements is necessary in order toreduce the high capital cost and energy requirements for thecapture process.4,5
Primary and secondary amines are known for their fastreaction rates and high heat of reaction due to formation ofcarbamates with CO2.
6 Consequently they require high energyfor the reaction reversion. Tertiary amines, on the other hand,have low heat of reactions due to formation of bicarbonates bybase catalysis of CO2 hydration7 and require relatively lowenergy for solvent regeneration. These amines generally havehigh CO2 loading capacity and low reaction rate.8,9 None of theamine types have ideal properties for CO2 absorption, so mixedamine systems have become very popular in order to exploit thefavorable properties of all types of amines.A new set of solvents have recently emerged, which may be
called phase change solvents. They have shown potential to
reduce the energy requirements for solvent regeneration. Thesesolvents either form precipitate, for example, the Alstom chilledammonia (CAP) process10 or form two liquid phases, forexample, the DMX process11 and thermomorphic biphasicsolvents (TBS) systems.12 The TBS solvent systems release theabsorbed CO2 in the desorber at a much lower temperature of80 °C or even below, compared to the conventional aqueousalkanolamine solutions, which is typically 120 °C. They formtwo liquid phases during solvent regeneration and become onephase again during absorption and revert back to two phasesupon heating and agitating in the desorber.13−15 In the DMXprocess developed by IFP Energies nouvelles, on the otherhand, the single phase solvent splits into two liquid phases afterCO2 absorption. The amine-rich phase with very low CO2
loading recycles back to the absorber without regeneration andonly the water-rich phase with very high CO2 loading goes tothe stripper for the thermal regeneration. Therefore, the energyconsumption for solvent regeneration can be lowered due toreduced liquid flow rate in the stripper.11
Two different amines, 2-(diethylamino)ethanol (DEEA) and3-(methylamino)propylamine (MAPA), are under investigationin this study. DEEA is a tertiary alkanolamine and MAPA hastwo amine functional groups, a primary and a secondary (seeFigure 1). Therefore, we can exploit the favorable properties ofamines by blending DEEA and MAPA. Their blends have anadditional advantage of making liquid−liquid split when reacted
Received: December 12, 2012Accepted: April 25, 2013Published: May 22, 2013
Article
pubs.acs.org/jced
© 2013 American Chemical Society 1918 dx.doi.org/10.1021/je3013167 | J. Chem. Eng. Data 2013, 58, 1918−1926
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Heat of Absorption of CO2 in Phase Change Solvents:2‑(Diethylamino)ethanol and 3‑(Methylamino)propylamineMuhammad Waseem Arshad,† Philip Loldrup Fosbøl,† Nicolas von Solms,† Hallvard Fjøsne Svendsen,‡
and Kaj Thomsen†,*†Department of Chemical and Biochemical Engineering, Center for Energy Resources Engineering (CERE), Technical University ofDenmark, Søltofts Plads Building 229, DK-2800 Kongens Lyngby, Denmark‡Department of Chemical Engineering, Norwegian University of Science and Technology (NTNU), NO-7491 Trondheim, Norway
ABSTRACT: Heat of absorption of CO2 in phase change solvents con-taining 2-(diethylamino)ethanol (DEEA) and 3-(methylamino)propyl-amine (MAPA) were measured as a function of CO2 loading at differenttemperatures using a commercially available reaction calorimeter. Thetested systems were aqueous single amines (5 M DEEA, 2 M MAPA,and 1 M MAPA) and aqueous amine mixtures (5 M DEEA + 2 M MAPAand 5 M DEEA + 1 M MAPA) which give two liquid phases on react-ing with CO2. All parallel experiments have shown good repeatability.The measurements were taken isothermally at three different temper-atures, (40, 80, and 120) °C. The measured differential heat of absorp-tion values were converted into integral values by integration. Heats ofabsorption of CO2 in aqueous single amines were affected by changingthe solvent composition (large difference in concentrations) and CO2feed pressure simultaneously. In addition to these two parameters, it also depends on temperature and the type of amine used.Tertiary alkanolamine (DEEA) has shown greater dependency on these parameters compared to the diamine (MAPA)containing both primary and secondary amine functional groups. In aqueous amine mixtures, heats of absorption depend on CO2loading, temperature, and composition of the constituent amines in the mixture. All measured heat of absorption data werecompared with 30 mass % MEA used as a base case.
1. INTRODUCTION
Amine scrubbing is one of the most common postcombustionCO2 capture technologies available today. Owing to its extensiveuse in different industrial applications, for example, CO2 removalfrom reformer gases, natural gas sweetening etc.,1 it has beenconsidered as the most feasible route for the postcombustioncapture. These amine scrubbing processes selectively absorbCO2 from the flue gases and release a high-purity CO2 offgasstream upon heating in a stripper which is suitable for storagewithout any further treatment. However, it is well-known thatthese processes are energy intensive.2,3 Innovative process designand technological improvements are necessary in order to reducethe high capital cost and energy requirements for the captureprocesses.4 Besides this, it is also essential to develop solventsystems with improved energy efficiency while retaining thedesirable properties of fast reaction rate, high loading and cycliccapacities, low solvent degradation, low corrosiveness, and beingenvironmental friendly, etc. For energy efficient solvent systems,besides reasonable heat of absorption, the equilibrium temper-ature sensitivity should also be high in order to reduce the needfor stripping steam.5
Single amine solvent systems for CO2 capture were extensivelystudied and reported in the open literature. Primary and sec-ondary amines are very reactive toward CO2 as they form car-bamates. They have high heats of reaction and fast reaction
rates.6 Consequently, high energy is required for the solventregeneration. Tertiary amines, on the other hand, form bicar-bonates due to base catalysis of CO2 hydration.
7 They have lowheats of reaction leading to low energy requirements for thereaction reversion. These amines generally have high CO2loading capacity and a low reaction rate.8,9 Each type of aminegroup is associated with its own merits and demerits. Therefore,amine blends have become an attractive choice to exploit thefavorable properties of both amine types. Various amine blends(e.g., MEA + MDEA) have been studied and reported in theliterature.10,11
Recently, a new class of mixed amine solvent systems is emerg-ing, which may be called phase change solvents. They haveshown a potential to reduce the solvent regeneration energy.These phase change solvents either form precipitates on CO2
absorption such as the Alstom chilled ammonia process (CAP)12
or make a liquid−liquid split, for example, the DMX process13,14
and thermomorphic biphasic solvents (TBS) systems.15 TheTBS systems, after CO2 absorption, regenerate at a relativelylower temperature of 80 °C compared to the regenerationtemperature of conventional alkanolamine solutions (∼120 °C).
Received: February 7, 2013Accepted: May 30, 2013Published: June 17, 2013
Article
pubs.acs.org/jced
© 2013 American Chemical Society 1974 dx.doi.org/10.1021/je400289v | J. Chem. Eng. Data 2013, 58, 1974−1988
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Equilibrium Total Pressure and CO2 Solubility in Binaryand Ternary Aqueous Solutions of 2‑(Diethylamino)ethanol(DEEA) and 3‑(Methylamino)propylamine (MAPA)Muhammad Waseem Arshad,† Hallvard Fjøsne Svendsen,‡ Philip Loldrup Fosbøl,† Nicolas von Solms,†
and Kaj Thomsen*,†
†Department of Chemical and Biochemical Engineering, Center for Energy Resources Engineering (CERE), Technical University ofDenmark (DTU), Søltofts Plads Building 229, DK-2800 Kongens Lyngby, Denmark‡Department of Chemical Engineering, Norwegian University of Science and Technology (NTNU), NO-7491 Trondheim, Norway
ABSTRACT: Equilibrium total pressures were measured andequilibrium CO2 partial pressures were calculated from themeasured total pressure data in binary and ternary aqueous solutionsof 2-(diethylamino)ethanol (DEEA) and 3-(methylamino)-propylamine (MAPA). The measurements were carried out ina commercially available calorimeter used as an equilibriumcell. The examined systems were the binary aqueous solutionsof 5 M DEEA, 2 M MAPA, and 1 M MAPA and the ternaryaqueous mixtures of 5 M DEEA + 2 M MAPA (5D2M) and5 M DEEA + 1 M MAPA (5D1M), which gave liquid−liquidphase split upon CO2 absorption. The total pressures were measured and the CO2 partial pressures were calculated as a functionof CO2 loading at three different temperatures 40 °C, 80 °C, and 120 °C. All experiments were reproduced with goodrepeatability. The measurements were carried out for 30 mass % MEA solutions to validate the experimental method. All themeasured data were also compared with the results of 30 mass % MEA as a reference case. 5 M DEEA has shown high cycliccapacity. Both 2 M and 1 M MAPA showed high loading capacities at 40 °C and 120 °C. The aqueous amine mixtures, 5D2Mand 5D1M, gave fairly good cyclic capacities and their results depend on the concentration of the promoter (MAPA) in themixture. Approximate enthalpies of absorption of CO2 in all the tested aqueous amine systems were estimated from the CO2solubility data. The measured total pressure and the estimated CO2 solubility data can be useful in thermodynamic modeling ofthe capture systems when aqueous DEEA−MAPA solutions are used as capture solvents.
1. INTRODUCTION
Carbon dioxide (CO2) is a well-known greenhouse gas and amajor contributor to the global warming.1 Fossil fuel basedpower generation is one of the major sources of CO2 emissionsworldwide.2 The other large CO2 emitting point sources areiron and steel industry, cement production plants, refineries,natural gas processing plants, and petrochemical productionplants.3 Carbon capture and storage (CCS) is considered as apotential solution to reduce the CO2 emissions and to mitigatethe climate change.4 Among the available CCS technologies,the amine based absorption−desorption capture process isconsidered as the most mature technology due to its extensiveuse in different industrial application such as acid gas removalfrom natural gas.5 This technology can be retrofitted to theexisting power generation plants, and the techno-economicfeasibility studies indicate that the technology will remaincompetitive in the coming future.6,7 However, the majorchallenge with the amine scrubbing is the high energyrequirements of the process.8 Technical improvements in thecapture process and improved process design are one way toreduce the high energy demand of the process, the other beingthe design of energy efficient solvent systems.9
On the basis of the characteristics of different groups ofamines, several amine-based solvent systems have been studiedand reported in the literature. A few examples are (a) aqueoussingle alkanolamine solutions such as primary (monoethanol-amine, MEA), secondary (diethanolamine, DEA), and tertiary(triethanolamine, TEA, and methyldiethanolamine, MDEA)alkanolamines,5 (b) aqueous amine blends (tertiary amineblended with primary or secondary amines as a promoter suchas MEA + MDEA and DEA + MDEA)10 to exploit the favorableproperties of different types of amines, and (c) sterically hinderedamines11 and cyclic amine (e.g., piperazine)12 both as singleaqueous solutions13−15 or as a blend of both together16−18 or ablend of each with other amines.19−21 One of the basic purposes ofthese and many other studies reported in the literature is to get thebest solvent system with the characteristics of high CO2 loadingand cyclic capacity, fast reaction kinetics, low heat of absorption,low thermal and chemical degradation, low corrosion tendency,environmentally benign, and possibility of operating at elevated
Received: October 4, 2013Accepted: January 7, 2014Published: February 3, 2014
Article
pubs.acs.org/jced
© 2014 American Chemical Society 764 dx.doi.org/10.1021/je400886w | J. Chem. Eng. Data 2014, 59, 764−774
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Binary and ternary VLE of the 2-(diethylamino)-ethanol(DEEA)/3-(methylamino)-propylamine (MAPA)/water system
Ardi Hartono a, Fahad Saleem a, Muhammad Waseem Arshad b, Muhammad Usman a,Hallvard F. Svendsen a,n
a Department of Chemical Engineering, Norwegian University of Science and Technology, N-7491 Trondheim, Norwayb Technical University of Denmark, Søltofts Plads, 2800 Lyngby, Denmark
H I G H L I G H T S
� Binary, ternary VLE data measured for DEEA/H2O, DEEA/MAPA and DEEA/MAPA/H2O.� Titration technique developed to quantify the DEEA/MAPA system.� The UNIQUAC framework implemented and the parameters are fitted.� Activity coefficients of DEEA/MAPA in ternary found lower than for binary systems.� An inconsistency seen between water activity coefficients from VLE and SLE results.
a r t i c l e i n f o
Article history:Received 22 April 2013Received in revised form21 June 2013Accepted 28 June 2013Available online 9 July 2013
Keywords:VLEAlkalinityDEEAMAPAAbsorptionModeling
a b s t r a c t
A mixed 2-(diethylamino)-ethanol (DEEA) and 3-(methylamino)-propylamine (MAPA) system could bean attractive alternative solvent to improve the performance of CO2 capture for low partial pressurecases. This solvent has the advantages of forming two liquid phases upon CO2 loading, one rich in CO2
and the other very low in CO2. Having a highly concentrated rich solvent improvements could be reachedby reducing the sensible heat and improving the equilibrium sensitivity hence reducing the need forstripping steam. Also it is possible that the heat of absorption may change to the better.
To better understand this system in designing the separation unit requires substantial work oncharacterization of the solvent. One important aspect is to provide equilibrium data. In this work newebulliometric VLE data for the binary DEEA/H2O and DEEA/MAPA systems and the ternary DEEA/MAPA/H2O system are reported at different temperatures and concentrations. Results show that pure MAPA ismore volatile than DEEA, but in aqueous solution MAPA was found to be less volatile. A mix of DEEA andMAPA in aqueous solution tends to lower the volatility thus makes the system more advantageous byreducing volatility. The activity coefficients for the species in the ternary aqueous system are found to belower than the activity coefficients obtained from the corresponding binary aqueous mixtures.
The UNIQUAC framework was implemented to represent the experimental data. The six UNIQUACparameters were determined and were able to predict P-T-x-y, activity coefficient, excess enthalpy andfreezing point depression for both the binary and ternary systems. However, a small inconsistency wasobserved between water activity coefficients determined from ebulliometer and freezing point depres-sion measurements.
& 2013 Elsevier Ltd. All rights reserved.
1. Introduction
Amine mixtures which potentially form two phases at higher CO2
concentration have recently received attention as a CCS technology.The changes in technology comprises two major elements, solventand process development. When two phases occur the regeneration
heat requirement could be expected to be lower as only a lowerphase, being a highly concentrated rich solvent is sent to the stripperand the sensible heat loss could be reduced. By forming a secondphase the equilibrium temperature sensitivity could be improvedthereby reducing the need for stripping steam and also the heat ofabsorption may be affected positively.
The DMX process by IFPEN is based on special solvents formingtwo immiscible phases and is now under testing in Italy (Raynalet al., 2011). This process is claimed to give a specific reboiler duty aslow as 2.1 GJ/tonne CO2 captured which is significantly lower than
Contents lists available at SciVerse ScienceDirect
journal homepage: www.elsevier.com/locate/ces
Chemical Engineering Science
0009-2509/$ - see front matter & 2013 Elsevier Ltd. All rights reserved.http://dx.doi.org/10.1016/j.ces.2013.06.052
n Corresponding author. Tel.: +47 73594100; fax: +47 73594080.E-mail address: [email protected] (H.F. Svendsen).
Chemical Engineering Science 101 (2013) 401–411
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Energy Procedia 37 ( 2013 ) 1532 – 1542
1876-6102 © 2013 The Authors. Published by Elsevier Ltd.Selection and/or peer-review under responsibility of GHGTdoi: 10.1016/j.egypro.2013.06.029
GHGT-11
Heat of Absorption of CO2 in Aqueous Solutions of DEEA, MAPA and their Mixture
Muhammad Waseem Arshada, Nicolas von Solmsa, Kaj Thomsena, Hallvard Fjøsne Svendsenb,*
1. Introduction
aTechnical University of Denmark, Department of Chemical and Biochemical Engineering, Center for Energy Resources
Engineering (CERE), Søltofts Plads Building 229, DK-2800 Kongens Lyngby, Denmark bNorwegian University of Science and Technology (NTNU), Department of Chemical Engineering, NO-7491 Trondheim, Norway
Abstract
A reaction calorimeter was used to measure the differential heat of absorption of CO2 in phase change solvents as a function of temperature, CO2 loading and solvent composition. The measurements were taken for aqueous solutions of 2-(diethylamino)ethanol (DEEA), 3-(methylamino)propylamine (MAPA) and their mixture. The tested compositions were 5M DEEA, 2M MAPA and their mixture, 5M DEEA + 2M MAPA which gives two liquid phases on reacting with CO2. Experimental measurements were also carried out for 30% MEA used as a base case. The measurements were taken isothermally at three different temperatures 40, 80 and 120oC at a CO2 feed pressure of 600 kPa. In single aqueous amine solutions, heat of absorption increases with increase in temperature and depends on the type of amine used. DEEA, a tertiary amine, has lower heat of absorption compared to MAPA being a diamine with primary and secondary amine functional groups. For amine mixtures, heat of absorption is a function of CO2 loading and temperature. The heat of absorption against CO2 loading depends on the composition of the amines in the mixture. All the measured data in this work were compared with 30% MEA at absorption (40oC) and desorption (120oC) conditions.
Keywords: Heat of absorption; Calorimeter; Phase change solvents; CO2 capture; DEEA; MAPA
Carbon dioxide absorption using amines is the most common operation for CO2 capture from power plant flue gases. The amine-based absorption processes selectively absorb CO2 and release a high-purity
* Corresponding author. Tel.: +47 7359 4100; fax: +47 7359 4080. E-mail address: [email protected].
Available online at www.sciencedirect.com
© 2013 The Authors. Published by Elsevier Ltd.Selection and/or peer-review under responsibility of GHGT
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Published: November 14, 2011
r 2011 American Chemical Society 5088 dx.doi.org/10.1021/je200959m | J. Chem. Eng. Data 2011, 56, 5088–5093
ARTICLE
pubs.acs.org/jced
Aqueous Solubility of Piperazine and 2-Amino-2-methyl-1-propanolplus Their Mixtures Using an Improved Freezing-Point DepressionMethodPhilip Loldrup Fosbøl,* Randi Neerup, Muhammad Waseem Arshad, Zacarias Tecle, and Kaj Thomsen
Department of Chemical and Biochemical Engineering, Center for Energy Resources Engineering (CERE), Technical University ofDenmark (DTU), Søltofts Plads, Building 229, DK-2800 Kongens Lyngby, Denmark
ABSTRACT: In this work the solid�liquid equilibrium (SLE) and freezing-point depression (FPD) in the electrolytic binaryaqueous systems piperazine (PZ, CAS No. 110-85-0) and aqueous 2-amino-2-methyl-1-propanol (AMP, CAS No. 124-68-5) weremeasured. The FPD and solubility were also determined in the ternary AMP�PZ�H2O system. Amethod was developed by whichsolubility can be determined at higher temperatures using the FPD setup. A total of 86 data points are listed in the full concentrationrange from (�35 to 90) �C. The solid phases piperazine hexahydrate (PZ 3 6H2O), piperazine hemihydrate (PZ 3 1/2H2O), andanhydrous PZ precipitated during the experiments. The data can be used in the formulation, prevention, or intentional formation ofslurries in piperazine solvents for promoting CO2 capture using absorption and desorption.
1. INTRODUCTION
CO2 capture is an openly debated topic for carbon emissionreduction to reduce pollution by greenhouse gases. Processstreams containing carbon dioxide can be cleaned by absorptionin aqueous liquid solvents. Amines, strong bases, or combinationof the two are typically used as active components. The low heatsof absorption and desorption are design criteria that reduce thecost of energy in regeneration of the solvent. This is obtained byusing sterically hindered amines. The result is often slow reactionkinetics between the solvent and CO2. Consequently piperazine(PZ) is being used in solution formulation to create an enhancedCO2 capture solvent. PZ can be used with both amine and potashsolutions (K2CO3) to increase the rate of absorption and therebypromote the CO2 capture.
A lower PZ concentration was typically used in literature.Recently the scope has changed, and PZ is now being used athigher concentrations. On increasing the concentration, thesolubility limit of PZ is being reached, especially during wintertemperatures and even up to room temperature. The unexpectedformation of slurries and solids downstream may create unfore-seen process conditions, decrease efficiency, and create cloggingwhich will result in unfortunate hazardous operations. In generalit could be interesting to provoke the formation of CO2 contain-ing solids and thereby facilitate and increase the capacity ofthe capture solvent. CO2 deprived solids are rarely preferable interms of CO2 capture.
The aim of this work is to determine the solid�liquid phaseboundary in the two binary PZ�H2O and AMP�H2O systemsand also in the ternary AMP�PZ�H2O system. 2-Amino-2-methyl-1-propanol (AMP) is a sterically hindered amine. CO2
absorption in AMP solutions can be promoted by adding PZ.An additional goal of this work was to enhance the utiliza-
tion of freezing-point depression (FPD) equipment develop-ing a method for the purpose of studying solid�liquid equi-librium (SLE) behavior in solutions precipitating solids otherthan ice.
PZ is a compound which has a variety of applications; forexample, it has been used for animal and human intake in thetreatment of roundworm infections as an anthelmintic.1,2
The SLE phase boundaries of the aqueous PZ system wereexamined very early by Berthelot,3 further by Rosso andCarbonnel,4 and in summary by Carbonnel and Rosso.5 Berthelot3
stated the existence of the hexahydrate PZ 3 6H2O, the hemihy-drate PZ 3 1/2H2O, and possibly a monohydrate. The differentialscanning calorimetry (DSC) analysis by Rosso and Carbonnel4
confirmed the formation of the following PZ solid hydratephases, hexahydrate, hemihydrate, and anhydrous PZ with theequilibrium reactions:
PZ 3 6H2OðsÞ a PZðaqÞ þ 6H2OðlÞ ð1Þ
PZ 312H2OðsÞ a PZðaqÞ þ 1
2H2OðlÞ ð2Þ
PZðsÞ a PZðaqÞ ð3Þ
Rosso and Carbonnel especially note that the system hastwo eutectic points, at�1 �C between ice and hexahydrate andat 33 �C between hexahydrate and hemihydrate, including aperitectic point at 58 �C at the intersection between hemihydrateand anhydrous PZ. The hexahydrate melts at 44 �C, andanhydrous PZ melts at 104 �C, as determined by Berthelot,3
Schwarzenbach,6 and Rosso and Carbonnel.4 A more accurateanhydrous melting point was estimated by Witschonke7 of(111.4 and 111) �C by Hetzer et al.,8 which is in line with thechemical supplier of this work. Rosso and Carbonnel4 present a
Special Issue: Kenneth N. Marsh Festschrift
Received: September 5, 2011Accepted: November 8, 2011
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Energy Procedia 51 ( 2014 ) 217 – 223
Available online at www.sciencedirect.com
ScienceDirect
1876-6102 © 2013 Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).Selection and peer-review under responsibility of SINTEF Energi ASdoi: 10.1016/j.egypro.2014.07.025
7th Trondheim CCS Conference, TCCS-7, June 5-6 2013, Trondheim, Norway
Equilibrium Solubility of CO2 in Alkanolamines
Muhammad Waseem Arshada, Philip Loldrup Fosbøla, Nicolas von Solmsa, Hallvard Fjøsne Svendsenb, Kaj Thomsena,*
aTechnical University of Denmark, Department of Chemical and Biochemical Engineering, Center for Energy Resources Engineering (CERE), Søltofts Plads Building 229, DK-2800 Kongens Lyngby, Denmark
bNorwegian University of Science and Technology (NTNU), Department of Chemical Engineering, NO-7491 Trondheim, Norway
Abstract
Equilibrium solubility of CO2 were measured in aqueous solutions of Monoethanolamine (MEA) and N,N-diethylethanolamine (DEEA). Equilibrium cells are generally used for these measurements. In this study, the equilibrium data were measured from the calorimetry. For this purpose a reaction calorimeter (model CPA 122 from ChemiSens AB, Sweden) was used. The advantage of this method is being the measurement of both heats of absorption and equilibrium solubility data of CO2 at the same time. The measurements were performed for 30 mass % MEA and 5M DEEA solutions as a function of CO2 loading at three different temperatures 40, 80 and 120oC. The measured 30 mass % MEA and 5M DEEA data were compared with the literature data obtained from different equilibrium cells which validated the use of calorimeters for equilibrium solubility measurements. © 2013 The Authors. Published by Elsevier Ltd. Selection and peer-review under responsibility of SINTEF Energi AS.
Keywords: Equilibrium CO2 solubility; Vapor-liquid equilibrium; Calorimeter; Post-combustion capture; Alkanolamines; Monoethanolamine (MEA); N,N-diethylethanolamine (DEEA)
* Corresponding author. Tel.: +45 4525 2860; fax: +45 4588 2258.
E-mail address: [email protected]
© 2013 Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).Selection and peer-review under responsibility of SINTEF Energi AS
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Center for Energy Resources Engineering
Department of Chemical and
Biochemical Engineering
Technical University of Denmark
Søltofts Plads, Building 229
DK-2800 Kgs. Lyngby
Denmark
Phone: +45 4525 2800
Fax: +45 4525 4588
Web: www.cere.dtu.dk
ISBN : 978-87-93054-55-4