Grating light reflection spectroelectrochemistry for detection of trace amounts of aromatic hydrocarbons in water

KELLY,MICHAEL J. ; SWEATT,WILLIAM C. ; KEMME,SHANALYN A. ; KASUNIC,K.J. ; BLAIR,DIANNA S. ; ZAIDI,S.H. ; MCNEIL,J.R. ; BURGESS,L.W. ; BRODSKY,A.M. ; SMITH,S.A.

Sandia National Laboratories

关键词: Electrochemical Cells;    Tnt;    37 Inorganic, Organic, Physical And Analytical Chemistry;    Polycyclic Aromatic Hydrocarbons;    Optical Spectrometers;   

DOI  :  10.2172/754395
RP-ID  :  SAND2000-1018
RP-ID  :  AC04-94AL85000
RP-ID  :  754395

美国|英语

来源: UNT Digital Library

【 摘 要 】

Grating light reflection spectroscopy (GLRS) is an emerging technique for spectroscopic analysis and sensing. A transmission diffraction grating is placed in contact with the sample to be analyzed, and an incident light beam is directed onto the grating. At certain angles of incidence, some of the diffracted orders are transformed from traveling waves to evanescent waves. This occurs at a specific wavelength that is a function of the grating period and the complex index of refraction of the sample. The intensities of diffracted orders are also dependent on the sample's complex index of refraction. The authors describe the use of GLRS, in combination with electrochemical modulation of the grating, for the detection of trace amounts of aromatic hydrocarbons. The diffraction grating consisted of chromium lines on a fused silica substrate. The depth of the grating lines was 1 {micro}m, the grating period was 1 {micro}m, and the duty cycle was 50%. Since chromium was not suitable for electrochemical modulation of the analyte concentration, a 200 nm gold layer was deposited over the entire grating. This gold layer slightly degraded the transmission of the grating, but provided satisfactory optical transparency for the spectroelectrochemical experiments. The grating was configured as the working electrode in an electrochemical cell containing water plus trace amounts of the aromatic hydrocarbon analytes. The grating was then electrochemically modulated via cyclic voltammetry waveforms, and the normalized intensity of the zero order reflection was simultaneously measured. The authors discuss the lower limits of detection (LLD) for two analytes, 7-dimethylamino-1,2-benzophenoxazine (Meldola's Blue dye) and 2,4,6-trinitrotoluene (TNT), probed with an incident HeNe laser beam ({lambda} = 543.5 nm) at an incident angle of 52.5{degree}. The LLD for 7-dimethylamino-1,2-benzophenoxazine is approximately 50 parts per billion (ppb), while the LLD for TNT is approximately 50 parts per million (ppm). The possible factors contributing to the differences in LLD for these analytes are discussed. This is the final report for a Sandia National Laboratories Laboratory Directed Research and Development (LDRD) project conducted during fiscal years 1998 and 1999 (case number 3518.190).