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Frontiers of Chemical Science and Engineering

ISSN 2095-0179

ISSN 2095-0187(Online)

CN 11-5981/TQ

Postal Subscription Code 80-969

2018 Impact Factor: 2.809

Front. Chem. Sci. Eng.    2020, Vol. 14 Issue (3) : 415-424    https://doi.org/10.1007/s11705-019-1882-4
RESEARCH ARTICLE
Precipitation study of CO2-loaded glycinate solution with the introduction of ethanol as an antisolvent
Siming Chen1, Yue Wu2, Geoffrey W. Stevens2, Guoping Hu2, Wenshou Sun1(), Kathryn A. Mumford2()
1. College of Environmental Sciences and Engineering, Qingdao University, Qingdao 266071, China
2. Peter Cook Centre for Carbon Capture and Storage Research (PCC), Particulate Fluids Processing Centre (PFPC), Department of Chemical Engineering, University of Melbourne, Parkville, Victoria 3010, Australia
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Abstract

Focused beam reflectance measurement (FBRM) and 13C nuclear magnetic resonance (13C NMR) analysis were used to study the precipitation process of CO2-loaded potassium glycinate (KGLY) solutions at different CO2 loadings, during the addition of ethanol as an antisolvent at a rate of 10 mL·min−1. The volume ratio of ethanol added to the KGLY solution (3.0 mol·L−1, 340 mL) ranged from 0 to 3.0. Three solid-liquid-liquid phases were formed during the precipitation process. The FBRM results showed that the number of particles formed increased with CO2 loading and ethanol addition for CO2-unsaturated KGLY solutions, whilst for CO2-saturated KGLY solution it first increased then decreased to a stable value with ethanol addition. 13C NMR spectroscopic analysis showed that the crystals precipitated from the CO2-unsaturated KGLY solutions consisted of glycine only, and the quantity crystallised increased with CO2 loading and ethanol addition. However, a complex mixture containing glycine, carbamate and potassium bicarbonate was precipitated from CO2-saturated KGLY solution with the maximum precipitation percentages of 94.3%, 31.4% and 89.6%, respectively, at the ethanol volume fractions of 1.6, 2.5 and 2.3.

Keywords crystallization      precipitation      glycinate      FBRM      13C NMR     
Corresponding Author(s): Wenshou Sun,Kathryn A. Mumford   
Just Accepted Date: 11 September 2019   Online First Date: 30 October 2019    Issue Date: 28 April 2020
 Cite this article:   
Siming Chen,Yue Wu,Geoffrey W. Stevens, et al. Precipitation study of CO2-loaded glycinate solution with the introduction of ethanol as an antisolvent[J]. Front. Chem. Sci. Eng., 2020, 14(3): 415-424.
 URL:  
https://academic.hep.com.cn/fcse/EN/10.1007/s11705-019-1882-4
https://academic.hep.com.cn/fcse/EN/Y2020/V14/I3/415
Fig.1  Three forms of amino acids: Cationic, anionic and zwitterionic.
Fig.2  CO2 absorption apparatus.
Fig.3  Crystallization measurement flowchart using Optimax and FBRM. 1. Baffle blade; 2. stirrer; 3. FBRM; 4. temperature sensor; 5. water bath; 6. reactor; 7. thermostat; 8. pipe; 9. cover; 10. dosing unit.
Fig.4  The molecular structures and type of nuclei assignment.
Fig.5  Crystallization characteristics of the CO2-loaded KGLY solutions upon the addition of ethanol.
Fig.6  13C NMR spectra of the CO2-loaded KGLY solutions.
Fig.7  Species distribution in the KGLY solution during the CO2 absorption process.
Fig.8  Scheme 1 Reaction mechanism of CO2 with KGLY solution.
Fig.9  13C NMR spectra of the (a) upper liquid phase, (b) lower liquid phase and (c) solid phase formed at the ethanol volume fraction of 3.0 for CO2-loaded KGLY solutions with different CO2 loadings.
Fig.10  13C NMR spectra of the solid phase precipitated from the CO2-saturated KGLY solution at different ethanol volume fractions of 0.8, 1.6, 2.3, 2.5 and 3.0.
Fig.11  Variations of the precipitation percentage of glycine with ethanol volume fraction for the CO2-loaded KGLY solutions with different CO2 loadings.
Fig.12  Variations of the precipitation percentages of each species from the CO2-saturated KGLY solutions with ethanol volume fraction.
1 H Yang, Z Xu, M Fan, R Gupta, R B Slimane, A E Bland, I Wright. Progress in carbon dioxide separation and capture: A review. Acta Scientiae Circumstantiae, 2008, 20(1): 14–27
https://doi.org/10.1016/S1001-0742(08)60002-9
2 J Davison, K Thambimuthu. An overview of technologies and costs of carbon dioxide capture in power generation. Proceedings of the Institution of Mechanical Engineers. Part A, Journal of Power and Energy, 2009, 223(3): 201–212
https://doi.org/10.1243/09576509JPE625
3 F Y Jou, A E Mather, F D Otto. The solubility of CO2 in a 30 mass% monoethanolamine solution. Canadian Journal of Chemical Engineering, 1995, 73(1): 140–147
https://doi.org/10.1002/cjce.5450730116
4 R J Hook. An investigation of some sterically hindered amines as potential carbon dioxide scrubbing compounds. Industrial & Engineering Chemistry Research, 1997, 36(5): 1779–1790
https://doi.org/10.1021/ie9605589
5 D E Penny, T J Ritter. Kinetic study of the reaction between carbon dioxide and primary amines. Journal of the Chemical Society, Faraday Transactions, 1983, 9(9): 2103–2109
https://doi.org/10.1039/f19837902103
6 G T Rochelle. New amines for CO2 capture. II. Oxidative degradation mechanisms. Current Opinion in Chemical Engineering, 2012, 1(2): 183–190
https://doi.org/10.1016/j.coche.2012.02.004
7 D W Park, Y S Son, D W Park, K J Oh. Absorption of carbon dioxide into aqueous solution of sodium glycinate. Separation Science and Technology, 2008, 43(11-12): 3003–3019
https://doi.org/10.1080/01496390802219620
8 P S Kumar, J A Hogendoorn, G F Versteeg, P H M Feron. Kinetics of the reaction of CO2 with aqueous potassium salt of taurine and glycine. AIChE Journal. American Institute of Chemical Engineers, 2010, 49(1): 203–213
https://doi.org/10.1002/aic.690490118
9 G Hu, K H Smith, L Liu, S E Kentish, G W Stevens. Reaction kinetics and mechanism between histidine and carbon dioxide. Chemical Engineering Journal, 2017, 307(1): 56–62
https://doi.org/10.1016/j.cej.2016.08.066
10 J V Holst, G F Versteeg, D W F Brilman, J A Hogendoorn. Kinetic study of CO2 with various amino acid salts in aqueous solution. Chemical Engineering Science, 2009, 64(1): 59–68
https://doi.org/10.1016/j.ces.2008.09.015
11 P Kumar, J Hogendoorn, G Versteeg, P Feron. Kinetics of the reaction of CO2 with aqueous potassium salt of taurine and glycine. AIChE Journal. American Institute of Chemical Engineers, 2003, 49(1): 203–213
https://doi.org/10.1002/aic.690490118
12 A F Portugal, J M Sousa, F D Magalhães, A Mendes. Solubility of carbon dioxide in aqueous solutions of amino acid salts. Chemical Engineering Science, 2009, 64(9): 1993–2002
https://doi.org/10.1016/j.ces.2009.01.036
13 A P Hallenbeck, A Egbebi, K P Resnik, D Hopkinson, S L Anna, J R Kitchin. Comparative microfluidic screening of amino acid salt solutions for post-combustion CO2 capture. International Journal of Greenhouse Gas Control, 2015, 43: 189–197
https://doi.org/10.1016/j.ijggc.2015.10.026
14 J A Lim, D H Kim, Y Yoon, S K Jeong, K T Park, S C Nam. Absorption of CO2 into aqueous potassium salt solutions of L-alanine and L-proline. Energy & Fuels, 2012, 26(6): 3910–3918
https://doi.org/10.1021/ef300453e
15 M E Majchrowicz, D W F Brilman. Solubility of CO2 in aqueous potassium L-prolinate solutions-absorber conditions. Chemical Engineering Science, 2012, 72: 35–44
https://doi.org/10.1016/j.ces.2011.12.014
16 H Thee, N J Nicholas, K H Smith, G Da Silva, S E Kentish, G W Stevens. A kinetic study of CO2 capture with potassium carbonate solutions promoted with various amino acids: Glycine, sarcosine and proline. International Journal of Greenhouse Gas Control, 2014, 20(Suppl C): 212–222
https://doi.org/10.1016/j.ijggc.2013.10.027
17 E S Fernandez, K Heffernan, L V V D Ham, M J G Linders, E Eggink, F N H Schrama, D W F Brilman, E L V Goetheer, T J H Vlugt. Conceptual design of a novel CO2 capture process based on precipitating amino acid solvents. Industrial & Engineering Chemistry Research, 2013, 52(34): 12223–12235
https://doi.org/10.1021/ie401228r
18 R J Perry, B R Wood, S Genovese, M J O’Brien, T Westendorf, M L Meketa, R Farnum, J Mcdermott, I Sultanova, T M Perry, et al. CO2 capture using phase-changing sorbents. Energy & Fuels, 2012, 26(4): 2528–2538
https://doi.org/10.1021/ef300079w
19 S Seo, L D Simoni, M Ma, M A Desilva, Y Huang, M A Stadtherr, J F Brennecke. Phase-change ionic liquids for postcombustion CO2 capture. Energy & Fuels, 2014, 28(9): 5968–5977
https://doi.org/10.1021/ef501374x
20 L D Wang, S L An, Q W Li, S H Yu, S Y Wu. Phase change behavior and kinetics of CO2 absorption into DMBA/DEEA solution in a wetted-wall column. Chemical Engineering Journal, 2017, 314: 681–687
https://doi.org/10.1016/j.cej.2016.12.033
21 P S Kumar, J A Hogendoorn, P H M Feron, G F Versteeg. Equilibrium solubility of CO2 in aqueous potassium taurate solutions: Part 1. Crystallization in carbon dioxide loaded aqueous salt solutions of amino acids. Industrial & Engineering Chemistry Research, 2003, 42(12): 2832–2840
https://doi.org/10.1021/ie0206002
22 E S Fernandez, E L V Goetheer. DECAB: Process development of a phase change absorption process. Energy Procedia, 2011, 4(1): 868–875
https://doi.org/10.1016/j.egypro.2011.01.131
23 U E Aronu, A F Ciftja, I Kim, A Hartono. Understanding precipitation in amino acid salt systems at process conditions. Energy Procedia, 2013, 37: 233–240
https://doi.org/10.1016/j.egypro.2013.05.107
24 Y Y Bian, S F Shen. CO2 absorption into a phase change absorbent: Water-lean potassium prolinate/ethanol solution. Chinese Journal of Chemical Engineering, 2018, 26(11): 2318–2326
https://doi.org/10.1016/j.cjche.2018.02.022
25 P E Holmes, M Naaz, B E Poling. Ion Concentrations in the CO2-NH3-H2O system from 13C NMR spectroscopy. Industrial & Engineering Chemistry Research, 1998, 37(8): 3281–3287
https://doi.org/10.1021/ie9707782
26 H C Shi, A Naami, R Idem, T Sema, Z W Liang, P Usubharatana, C Saiwan, P Tontiwachwuthikul. NMR analysis of amine-CO2‒H2O systems with VLE modeling for CO2 capture processes. Future Medicinal Chemistry, 2013, 10: 10–31
27 H Shi, T Sema, A Naami, Z Liang, R Idem, P Tontiwachwuthikul. 13C NMR spectroscopy of a novel amine species in the DEAB–CO2–H2O system: VLE model. Industrial & Engineering Chemistry Research, 2012, 51(25): 8608–8615
https://doi.org/10.1021/ie300358c
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