2009
DOI: 10.1016/j.egypro.2009.01.102
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Oxidative degradation mechanisms for amines in flue gas capture

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Cited by 76 publications
(95 citation statements)
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“…Besides the emission of potentially harmful products, solvent degradation also impacts the process operating and capital costs. Indeed, the solvent absorption capacity decreases, its viscosity and its corrosivity increase, the vapour-liquid equilibrium is modified and foaming and fouling may appear in the columns (Bedell, 2009). So far, the process energy penalty and the degradation of amine solvents have been studied separately and previously published models of the CO 2 capture process did not consider solvent degradation at all (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…Besides the emission of potentially harmful products, solvent degradation also impacts the process operating and capital costs. Indeed, the solvent absorption capacity decreases, its viscosity and its corrosivity increase, the vapour-liquid equilibrium is modified and foaming and fouling may appear in the columns (Bedell, 2009). So far, the process energy penalty and the degradation of amine solvents have been studied separately and previously published models of the CO 2 capture process did not consider solvent degradation at all (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…The primary degradation compounds are formed by either electron or hydrogen abstraction mechanisms (ammonia, aldehyde) or oxidation products of some of these compounds (acids). The initial mechanisms are still unclear, but the general impression is that the mechanisms either start with abstraction of an electron from the lone pair of nitrogen or abstraction of hydrogen from the nitrogen, α-carbon, or β-carbon, or a combination of these depending on the amine structure, nature of oxidants, pH, solvent effects and concentrations (Bedell, 2009;Chi and Rochelle, 2002;Rochelle, 2004, 2006;Hull et al, 1967;Hull et al, 1969;Rosenblatt et al, 1967;Sexton, 2008) Secondary degradation compounds are formed by reactions between primary degradation compounds and amines forming for example amides as N-(2-hydroxyethyl)-formamide (HEF), N-(2-hydroxyethyl)-acetamide (HEA) and N,-oxamide (BHEOX) from MEA and acid, or aldehyde and oxygen, and imidazoles as N-(2-hydroxyethyl)imidazole (HEI) from ammonia, MEA and several aldehydes. Lately several mechanisms have been suggested for the formation of secondary degradation compounds (da Silva et al, 2012;Lepaumier et al, 2011a;Strazisar et al, 2003).…”
Section: Introductionmentioning
confidence: 99%
“…Indeed, MEA has strong interaction with oxygen (Supap et al, 2001(Supap et al, , 2006Bello and Idem, 2005;Chi and Rochelle, 2002;Goff andRochelle, 2004, 2006;Sexton and Rochelle, 2009;Bedell, 2009Bedell, , 2011Bedell et al, 2011;Lepaumier et al, 2009b, c). Working closer to the absorption conditions, Sexton and Rochelle (2009) have shown that ammonia is the major by-product in the gas phase and is a good indicator of MEA oxidative degradation.…”
Section: Potential Interactions With the Solvent And The Incinerator mentioning
confidence: 99%
“…It has been demonstrated that metal present in setup serves as catalyst for oxidize the reaction. Bedell (2009) proposed a pathway using radical mechanisms for the oxidative degradation. As summarized in Figure 2, the metal cation reacts with oxygen to generate radicals which attack the MEA molecules.…”
Section: Potential Interactions With the Solvent And The Incinerator mentioning
confidence: 99%