Direct Analysis in Real Time Mass Spectrometry (DART-MS) of Ionic Liquids
被引:8
作者:
Mazzotta, Michael G.
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机构:
Eastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USAEastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USA
Mazzotta, Michael G.
[1
]
Pace, Robert B.
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机构:
Eastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USA
Univ Kentucky, Ctr Appl Energy Res, Lexington, KY 40511 USAEastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USA
Pace, Robert B.
[1
,3
]
Wallgren, Brandy N.
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机构:
Murray State Univ, Dept Chem, Murray, KY 42071 USAEastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USA
Wallgren, Brandy N.
[2
]
Morton, Samuel A., III
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Univ Kentucky, Ctr Appl Energy Res, Lexington, KY 40511 USAEastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USA
Morton, Samuel A., III
[3
]
Miller, Kevin M.
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机构:
Murray State Univ, Dept Chem, Murray, KY 42071 USAEastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USA
Miller, Kevin M.
[2
]
Smith, Darrin L.
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机构:
Eastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USAEastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USA
Smith, Darrin L.
[1
]
机构:
[1] Eastern Kentucky Univ, Dept Chem, Richmond, KY 40475 USA
[2] Murray State Univ, Dept Chem, Murray, KY 42071 USA
[3] Univ Kentucky, Ctr Appl Energy Res, Lexington, KY 40511 USA
Direct analysis in real time (DART);
Ambient MS;
Ionic liquids;
Qualitative MS;
MOLECULAR-IONS;
GAS-PHASE;
ELECTROSPRAY;
IONIZATION;
SALTS;
D O I:
10.1007/s13361-013-0696-8
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Direct analysis in real time mass spectrometry (DART-MS) was used to analyze ionic liquids (ILs) containing either imidazolium or phosphonium cations combined with different types of inorganic and organic anions. Ionic liquids were directly inserted into the ionization source using a glass probe without dissolution into organic solvents. Mass spectra of the ILs were collected in both positive and negative mode with a linear ion-trap instrument. The intact cation of the compound was typically the dominant peak in positive mass spectra and cluster ion formation was present. Some individual anions were not readily observed in the negative mass spectra (based on the type of anion); however, the mass difference of adjacent cluster ions equal the mass of a complete IL and the anion mass could be verified by subtracting the known cation mass. The degree and intensity of the cluster ion formations was found to be dependent on the nature of the specific ILs as well as the DART temperature gas stream.
机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Gozzo, FC
;
Santos, LS
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机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Santos, LS
;
Augusti, R
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机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Augusti, R
;
Consorti, CS
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机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Consorti, CS
;
Dupont, J
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机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Dupont, J
;
Eberlin, MN
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机构:
Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Gozzo, FC
;
Santos, LS
论文数: 0引用数: 0
h-index: 0
机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Santos, LS
;
Augusti, R
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h-index: 0
机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Augusti, R
;
Consorti, CS
论文数: 0引用数: 0
h-index: 0
机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Consorti, CS
;
Dupont, J
论文数: 0引用数: 0
h-index: 0
机构:Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil
Dupont, J
;
Eberlin, MN
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h-index: 0
机构:
Univ Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, BrazilUniv Fed Rio Grande do Sul, Inst Chem, BR-91501970 Porto Alegre, RS, Brazil