AMPEROMETRIC DETERMINATION OF N-NITROSAMINES IN AQUEOUS-SOLUTION AT AN ELECTRODE COATED WITH A RUTHENIUM-BASED INORGANIC POLYMER

Authors
Citation
W. Gorski et Ja. Cox, AMPEROMETRIC DETERMINATION OF N-NITROSAMINES IN AQUEOUS-SOLUTION AT AN ELECTRODE COATED WITH A RUTHENIUM-BASED INORGANIC POLYMER, Analytical chemistry, 66(17), 1994, pp. 2771-2774
Citations number
27
Categorie Soggetti
Chemistry Analytical
Journal title
ISSN journal
00032700
Volume
66
Issue
17
Year of publication
1994
Pages
2771 - 2774
Database
ISI
SICI code
0003-2700(1994)66:17<2771:ADONIA>2.0.ZU;2-H
Abstract
The diffusion-limited electrochemical oxidation of N-nitrosamines in a n aqueous pH 1.5 buffer is demonstrated at a glassy carbon electrode w hich is coated with a film of mixed valent ruthenium oxides that are s tabilized by cyano crosslinks (mvRuCN). The process occurs at 1.080 V vs Ag/AgCl, 3 M NaCl where Ru(VI) is the electron-transfer mediator in the film. The mvRuCN electrode was used in a potentiostatic amperomet ric detector for flow injection analysis and highperformance liquid ch romatography to allow the determination of representative compounds su ch as N-nitrosodimethylamine, N-nitrosodi-n-propylamine (NNDPA), and N -nitrosodiphenylamine (NNDPhA). Using HPLC with a C-18 column, a linea r least squares calibration curve for NNDPA over the range 5.0 x 10(-8 ) to 1.0 X 10(-6) M (8 points) had a slope of 12.8 +/- 0.2 nA/mu M and a correlation coefficient of 0.999; the detection limit (signal equal to three times the noise) was 10 nM. The relative standard deviation of five replicate injections of 0.80 mu M NNDPhA was 2%. A pooled rela tive standard deviation over a 22-day period (15 sets, five trials per set) of 2% documents long-term stability.