TY - JOUR
T1 - Development of an Electrospray-63Ni-Differential Ion Mobility Spectrometer for the Analysis of Aqueous Samples
AU - Kuklya, Andriy
AU - Uteschil, Florian
AU - Kerpen, Klaus
AU - Marks, Robert
AU - Telgheder, Ursula
N1 - Funding Information: This work was financially supported by the Arbeitsgemeinschaft Industrieller Forschungsvereinigungen (AIF) , Cologne, (ZIM Project no. KF2210313AK3 ).
PY - 2014
Y1 - 2014
N2 - The feasibility of an electrospray coupled with a (63)Ni-differential ion mobility spectrometer (DMS) for the analysis of water samples was proven on examples of 2-hexanone, fluoroacetamide, l-nicotine and 1-phenyl-2-thiourea water solutions. The model substances were selected in order to cover the vapor pressure range of 0.3-1467 Pa. To reduce the inline humidity, which demonstrates a strong influence on the analyte compensation voltage, two units with a desolvation region lengths of 15.5 and 7 mm were examined. The counter gas (heated to 100 °C nitrogen) with flow rates of 100 mL min(-1) and 30 mL min(-1) for short and long desolvation units, respectively, was essential for the efficient reduction of humidity. The reduction of water content in the carrier gas to 2.2-2.4 g m(-3) and to 1.8-2.0 g m(-3) for the short and long desolvation unit, respectively, was achieved at an electrospray flow rate of 1000 nL min(-1). With this adjusted experimental setup, the detection of model substances in the water solutions, in the range of 0.1-50 mg L(-1), was performed. No correlation between the vapor pressure and signal area was observed. The high stability of the inline humidity, and the correspondingly stable carrier gas flow rate, were found to be essential for an acceptable reproducibility.
AB - The feasibility of an electrospray coupled with a (63)Ni-differential ion mobility spectrometer (DMS) for the analysis of water samples was proven on examples of 2-hexanone, fluoroacetamide, l-nicotine and 1-phenyl-2-thiourea water solutions. The model substances were selected in order to cover the vapor pressure range of 0.3-1467 Pa. To reduce the inline humidity, which demonstrates a strong influence on the analyte compensation voltage, two units with a desolvation region lengths of 15.5 and 7 mm were examined. The counter gas (heated to 100 °C nitrogen) with flow rates of 100 mL min(-1) and 30 mL min(-1) for short and long desolvation units, respectively, was essential for the efficient reduction of humidity. The reduction of water content in the carrier gas to 2.2-2.4 g m(-3) and to 1.8-2.0 g m(-3) for the short and long desolvation unit, respectively, was achieved at an electrospray flow rate of 1000 nL min(-1). With this adjusted experimental setup, the detection of model substances in the water solutions, in the range of 0.1-50 mg L(-1), was performed. No correlation between the vapor pressure and signal area was observed. The high stability of the inline humidity, and the correspondingly stable carrier gas flow rate, were found to be essential for an acceptable reproducibility.
KW - Aqueous samples
KW - Differential ion mobility spectrometry (DMS)
KW - Electrospray (ES)
KW - High field asymmetric waveform ion mobility spectrometry (FAIMS)
KW - Online monitoring
KW - Water monitoring
UR - http://www.scopus.com/inward/record.url?scp=84891072693&partnerID=8YFLogxK
M3 - مقالة
SN - 0039-9140
VL - 120
SP - 173
EP - 180
JO - Talanta
JF - Talanta
ER -