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Table 3 Compounds identified by the present study by using GC-MS and LC-MS-QTOF in AEEA/CO2/H2O system at 135 °C

From: Thermal degradation of aqueous 2-aminoethylethanolamine in CO2 capture; identification of degradation products, reaction mechanisms and computational studies

Compound

Abb.

MW (g/mol)

Structures

Analytical technique

Diethanolamine

DEA

105

GC–MS

LC-MS-QTOF

1-Piperazineethanol

HEP

126

GC–MS

LC-MS-QTOF

1,4-Bis(2-hydroxyethyl)piperazine

BHEP

130

GC–MS

LC-MS-QTOF

2-Imidazolidinone

HEI

86

GC–MS

1-(2-Hydroxyethyl)-2-imidazolidinone

HEIA

130

GC–MS

LC-MS-QTOF

2-((2-Aminoethyl)-(2-(2-aminoethylamino)-(ethylamino)ethanol

AAEEA*

191

2-hydroxyethyl-2-oxazolidone

HEOD

131

GC–MS

LC-MS-QTOF

Succinimide

Succ

99

GC–MS

N-Methylsuccinimide

MSucc

113

LC-MS-QTOF

N,N’-Dimethyl-2-imidazolidinone

DMDZ

114

GC–MS

4-[(2-Hydroxyethyl)(nitroso)amino]-1-butanol

HNAP

162

LC-MS-QTOF

1-Nitroso-4-piperidinol

NP

117

LC-MS-QTOF

4-[Butyl(nitroso)amino]-2-butanol

BNAB

173

LC-MS-QTOF

N-(Butyl(nitroso)amino)methyl)acetamide

BNAMA

173

LC-MS-QTOF

(3-Aminopropyl)morpholine

AMM

144

GC–MS

N-(2-hydroxyethyl)-N -methylpiperazine

MPE

144

GC–MS

1,4-Diformylpiperazine

DFP

142

GC–MS

Homoserine

Hom

119

GC–MS

1-Methyl-4-nitrosopiperazine

MNP

129

LC-MS-QTOF

Pyrazole-1-ethanol

PE

112

LC-MS-QTOF

1-Piperazineethanamine

AEP

129

GC–MS

1-(2-(2-Hydroxyethoxy)ethyl) piperazine

HEEP

174

GC–MS

LC-MS-Q TOF

N-[2-[3-[N-Aziridyl]propyl]aminoethyl]piperazine

APAP

212

GC–MS

Tetraethylenepentamine

TEP

191

GC–MS