2011
DOI: 10.1016/j.ces.2011.04.007
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Degradation of MMEA at absorber and stripper conditions

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Cited by 46 publications
(68 citation statements)
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“…Most of the amines tested showed very little oxidative degradation and this makes it difficult to propose degradation mechanisms for the formation of new degradation compounds. In general it seems like the formation of degradation compounds follows the same patterns as earlier described for the formation of de-methylated amines (secondary and tertiary amines) or secondary products as HEF analogues, HEI, OZD analogues, alkylamines and ammonia (da Silva et al, 2012; Lepaumier et al, 2011b;Lepaumier et al, 2009b;Strazisar et al, 2003;.…”
Section: Other Aminesmentioning
confidence: 63%
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“…Most of the amines tested showed very little oxidative degradation and this makes it difficult to propose degradation mechanisms for the formation of new degradation compounds. In general it seems like the formation of degradation compounds follows the same patterns as earlier described for the formation of de-methylated amines (secondary and tertiary amines) or secondary products as HEF analogues, HEI, OZD analogues, alkylamines and ammonia (da Silva et al, 2012; Lepaumier et al, 2011b;Lepaumier et al, 2009b;Strazisar et al, 2003;.…”
Section: Other Aminesmentioning
confidence: 63%
“…System and methods used for LC-MS analysis (alkylamine, ammonia, degradation compounds, amine, full scan) are described in more details by da Silva and Vevelstad (da Silva et al, 2012;. Details for the alkylamine and ammonia analysis for MEA experiment 1, KSAR and KGly on GC-MS are described by Vevelstad , while more thorough details on method and system used for the GC-MS analysis (MEA, MMEA, DMMEA, KSAR) of degradation compounds are given by Lepaumier (Lepaumier et al, 2011b). All systems and methods used for the rest of analyses, except "HSS", were described in detail in previous publications .…”
Section: Methodsmentioning
confidence: 99%
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