Chemical speciation of CO2 absorption in aqueous monoethanolamine investigated by in situ Raman spectroscopy

被引:59
作者
Wong, M. K. [1 ]
Bustam, M. A. [1 ]
Shariff, A. M. [1 ]
机构
[1] Univ Teknol PETRONAS, RCCO2C, Tronoh 31750, Perak, Malaysia
关键词
CO2; absorption; Peak fitting; Quantitative analysis; Raman spectroscopy; Speciation; Solubility; Vibrational assignment; CARBON-DIOXIDE; LIQUID-PHASE; QUANTITATIVE-ANALYSIS; SPECIES DISTRIBUTION; EQUILIBRIUM; SOLUBILITY; SYSTEM; CARBAMATE; NMR; BICARBONATE;
D O I
10.1016/j.ijggc.2015.05.016
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A quantitative analysis method of chemical species in liquid phase during CO2 absorption into monoethanolamine was developed for Raman spectroscopy. Band envelopes in the spectral region between 300 and 3100 cm(-1) were resolved with Gaussian Lorentzian function. Spectroscopic characterization of MEA, protonated MEA, carbamate, bicarbonate, carbonate and molecular CO2 in aqueous was performed. Calibration curves were constructed with area ratio plotted against species concentration. Concentration of individual chemical species in liquid phase can be systematically determined using the correlations introduced. Experiments of CO2 solubility in aqueous MEA were carried out for pressure ranges from 1 to 60 bar and three temperatures (303.15, 313.15 and 323.15) K with in situ Raman measurement. Absorption capacity was determined with conventional gas pressure drop method and newly developed Raman spectroscopic analysis method based on total carbon containing species in liquid phase. Results depict good accuracy and reproducibility of Raman measurement method. Chemical speciation during CO2 absorption into aqueous solution of 30% MEA at pressure up to 60 bar was evaluated. The findings from present work will improve the understanding of phase equilibrium behavior associated with absorption reactions and can be employed for monitoring, analysis and optimization of CO2 capture process. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:139 / 147
页数:9
相关论文
共 35 条
[1]   Carbon dioxide absorption into monoethanolamine in a continuous film contactor [J].
Akanksha ;
Pant, K. K. ;
Srivastava, V. K. .
CHEMICAL ENGINEERING JOURNAL, 2007, 133 (1-3) :229-237
[2]   Effect of methanol addition on water-CO2-diethanolamine system:: Influence on CO2 solubility and on liquid phase speciation [J].
Archane, A. ;
Gicquel, L. ;
Provost, E. ;
Fuerst, W. .
CHEMICAL ENGINEERING RESEARCH & DESIGN, 2008, 86 (6A) :592-599
[3]   In situ quantitative analysis of individual H2O-CO2 fluid inclusions by laser Raman spectroscopy [J].
Azbej, Tristan ;
Severs, Matthew J. ;
Rusk, Brian G. ;
Bodnar, Robert J. .
CHEMICAL GEOLOGY, 2007, 237 (3-4) :255-263
[4]   Online NMR spectroscopic study of species distribution in MEA-H2O-CO2 and DEA-H2O-CO2 [J].
Boettinger, Wolfram ;
Maiwald, Michael ;
Hasse, Hans .
FLUID PHASE EQUILIBRIA, 2008, 263 (02) :131-143
[5]   13C NMR as a method species determination in CO2 absorbent systems [J].
Ciftja, Arlinda F. ;
Hartono, Ardi ;
Svendsen, Hallvard F. .
INTERNATIONAL JOURNAL OF GREENHOUSE GAS CONTROL, 2013, 16 :224-232
[6]  
Coates J., 2006, ENCY ANAL CHEM, V12, P10815, DOI [DOI 10.1002/9780470027318.A5606, 10.1002/9780470027318.a5606]
[7]   A Vibrational-Spectroscopic Study of the Species Present in the CO(2)-H(2)O System [J].
Davis, A. R. ;
Oliver, B. G. .
JOURNAL OF SOLUTION CHEMISTRY, 1972, 1 (04) :329-339
[8]   RAMAN-SPECTRA, CONFORMATIONAL STABILITY AND NORMAL-COORDINATE ANALYSIS OF ETHYLMETHYLAMINE [J].
DECARVALHO, LAEB ;
TEIXEIRADIAS, JJC .
JOURNAL OF RAMAN SPECTROSCOPY, 1995, 26 (8-9) :653-661
[9]   Quantitative analysis of the liquid phase by FT-IR spectroscopy in the system CO2/diethanolamine (DEA)/H2O [J].
Diab, Farah ;
Provost, Elise ;
Laloue, Nicolas ;
Alix, Pascal ;
Souchon, Vincent ;
Delpoux, Olivier ;
Fuerst, Walter .
FLUID PHASE EQUILIBRIA, 2012, 325 :90-99
[10]   Chemical equilibrium constants for the formation of carbamates in (carbon dioxide plus piperazine plus water) from 1H-NMR-spectroscopy [J].
Ermatchkov, V ;
Kamps, APS ;
Maurer, G .
JOURNAL OF CHEMICAL THERMODYNAMICS, 2003, 35 (08) :1277-1289