New IR Fiber-Optic Chemical Sensor for in Situ Measurements of Chlorinated Hydrocarbons in Water

1993 ◽  
Vol 47 (9) ◽  
pp. 1484-1487 ◽  
Author(s):  
R. Krska ◽  
K. Taga ◽  
R. Kellner

In this work the development and validation of a new MIR fiber-optic physicochemical sensor system for the continuous in situ analysis of chlorinated hydrocarbons (CHCs) in water is described. This study took advantage of the selectivity and sensitivity of fiber evanescent wave spectroscopy (FEWS) and the recent development of polycrystalline silver halide fibers. Since these fibers are transparent up to 20 μm, it was possible for the first time to develop a fiber-optic sensing system for CHCs, which have their strongest absorption bands > 10 μm. The silver halide fibers were coated with low-density polyethylene (LDPE) to enrich the CHC within the evanescent wave and to exclude the IR absorbing water from the measurement. For the quantitative in situ FEWS measurements, the coated silver halide fibers were coupled to a Fourier transform infrared (FT-IR) spectrometer using an off-axis parabolic mirror and a fiber-detector coupling system. This setup enabled the simultaneous in situ detection of the most common chlorinated hydrocarbons in concentrations between 1 to 50 mg/L in water by employing a fiber sensing part only 10 cm in length. A comparative analysis of waste water samples under participation of two experienced head space-gas chromatography (HSGC) laboratories showed good agreement of this continuous sensor system with the established standard techniques. The resulting working curve for tetrachloroethylene showed a correlation coefficient of r2 = 0.968 and a relative standard deviation of 17% in the range from 1 to 10 ppm.

1994 ◽  
Vol 48 (3) ◽  
pp. 387-393 ◽  
Author(s):  
G. L. Klunder ◽  
J. BÜrck ◽  
H.-J. Ache ◽  
R. J. Silva ◽  
R. E. Russo

A coiled fiber-optic chemical sensor has proven to be effective for the remote detection of volatile organic compounds, such as trichloroethylene (TCE), 1,1-dichloroethylene (DCE), and gasoline, in aqueous solutions. The analyte diffuses into the hydrophobic cladding and evanescent wave absorption spectra are measured in the near-infrared (1600–1850 nm) without the presence of the water absorption bands. In order for fiberoptic chemical sensors to operate effectively in remote environments, the influence of temperature on the sensor response must be known. The C-H bonds of the polysiloxane cladding material also have absorption bands in the near-infrared (NIR). Changes in temperature will change the density (i.e., concentration of C-H bonds) and refractive index of the cladding. Due to these effects, a temperature change of only 3°C from the reference has been shown to significantly alter the background absorbance. The temperature-dependent background absorption is found to be linear with the slope, and the values are proportional to the absorption coefficient of the cladding material. The intercept of the absorbance vs. temperature plot is found to follow the first derivative of the fiber sensor transmission spectrum. Evanescent wave absorption spectra of TCE solutions have been corrected for temperature.


2003 ◽  
Vol 57 (6) ◽  
pp. 607-613 ◽  
Author(s):  
H. Steiner ◽  
M. Jakusch ◽  
M. Kraft ◽  
M. Karlowatz ◽  
T. Baumann ◽  
...  

A prototype mid-infrared sensor system for the determination of volatile organic pollutants in groundwater was developed and tested under real-world conditions. The sensor comprises a portable Fourier transform infrared spectrometer, coupled to the sensor head via mid-infrared transparent silver halide fiber-optic cables. A 10 cm unclad middle section of the 6-m-long fiber is coated with ethylene propylene copolymer in order to enrich the analytes within the penetration depth of the evanescent field protruding from the fiber sensor head. A mixture of tetrachloroethylene, dichlorobenzene, diethyl phthalate, and xylene isomers at concentrations in the low ppm region was investigated qualitatively and quantitatively in an artificial aquifer system filled with Munich gravel. This simulated real-world site at a pilot scale enables in situ studies of the sensor response and spreading of the pollutants injected into the system with controlled groundwater flow. The sensor head was immersed into a monitoring well of the aquifer system at a distance of 1 m downstream of the sample inlet and at a depth of 30 cm. Within one hour, the analytes were clearly identified in the fingerprint region of the IR spectrum (1300 to 700 cm−1). The results have been validated by head-space gas chromatography, using samples collected during the field measurement. Five out of six analytes could be discriminated simultaneously; for two of the analytes the quantitative results are in agreement with the reference analysis.


2003 ◽  
Vol 90 (1-3) ◽  
pp. 319-323 ◽  
Author(s):  
T Beyer ◽  
P Hahn ◽  
S Hartwig ◽  
W Konz ◽  
S Scharring ◽  
...  

1992 ◽  
Vol 342 (1-2) ◽  
pp. 202-202 ◽  
Author(s):  
R. Krska ◽  
K. Taga ◽  
R. Kellner ◽  
A. Messica ◽  
A. Katzir

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