Sensitive detection of biacetyl in liquid chromatography using time-resolved sensitized phosphorescence

1985 ◽  
Vol 57 (9) ◽  
pp. 1815-1818 ◽  
Author(s):  
Robert A. Baumann ◽  
Cees. Gooijer ◽  
Nel H. Velthorst ◽  
Roland W. Frei
1981 ◽  
Vol 35 (6) ◽  
pp. 525-531 ◽  
Author(s):  
David M. Fraley ◽  
Dennis A. Yates ◽  
Stanley E. Manahan ◽  
David Stalling ◽  
James Petty

ICP-AES was used for the simultaneous multiple element detection of trace metals species separated by high-pressure liquid chromatography (HPLC). The technique is demonstrated for the determination of nitrilotriacetic acid (NTA) and ethylenedia-minetetraacetic acid (EDTA) chelates of copper, zinc, calcium, and magnesium. Multi-element chromatograms were obtained using a 32-channel polychromator programmed to perform a series of time-resolved intensity integrations. Data were retrieved channel-by-channel and plotted in histographic form. Comparison with UV absorbance and single-channel ICP-AES tracings reveals that the histograms reflect reliable chromatographic data. Linearity and precision of the system were found to be good in the 20 to 2000 ng range.


2017 ◽  
Vol 98 (2) ◽  
pp. 674-680 ◽  
Author(s):  
Xiaofei Hu ◽  
Jingjing Yao ◽  
Fangyu Wang ◽  
Mengqi Yin ◽  
Yaning Sun ◽  
...  

1987 ◽  
Vol 65 (5) ◽  
pp. 965-969 ◽  
Author(s):  
Robert A. Baumann ◽  
Marry Schreurs ◽  
Cees Gooijer ◽  
Nel H. Velthorst ◽  
Roland W. Frei

The feasibility of time-resolved quenched phosphorescence as a detection method for chromate based on paired-ion reversed phase high performance liquid chromatography is shown. After separation detection is achieved by monitoring the time-resolved phosphorescence signal of biacetyl at 515 nm. Optimization of the time-resolution parameters of the luminescence detector results in a limit of detection of 1.4 × 10−7 M (2 ng on column) for chromate standard solutions. The linearity of the method is three orders of magnitude. Chromatograms of tap water and surface water samples spiked with chromate show the potential applicability of the method for real samples.


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