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Fluorescence sensors based on a trifluoroacetophone compound doped in ethyl cellulose (EC) thin films have been developed for the detection of methanol, ethanol, and 2-propanol (isopropanol, PriOH) vapors. Thin-film sensors are prepared with 4-dibutylamino-4’-(trifluoroacetyl)stilbene (Chromoionophore IX or CIX) as the fluorescent dye and its solution in EC was spin-coated onto glass slides. The luminescence intensity of the dye (555 nm) is quenched when exposed to alcohol vapor. Tested in the range of ca. 0 - 1.5 × 104 ppm (wt) for MeOH and EtOH, and ca. 0 - 2.3 × 104 ppm for PriOH, the sensors gave detection limits of 9, 13, 21 ppm and quantification limits of 32, 43, and 70 ppm, respectively. To enhance the sensitivity of the sensors, TiO2 particles have been added to the films to induce Mie scattering, which increases the incident light interaction with the sensing films. The sensors in this work have been designed to work in a multianalyte platform for the simultaneous detection of multiple gas analytes.

A bismuth bulk electrode (BiBE) has been investigated as an alternative electrode for the anodic stripping voltammetric (ASV) analysis of Pb(II), Cd(II), and Zn(II). The BiBE, which is fabricated in-house, shows results comparable to those of similar analyses at other Bi-based electrodes. Metal accumulation is achieved by holding the electrode potential at -1.4V (vs. Ag/AgCl) for 180 s followed by a square wave voltammetric stripping scan from -1.4 to -0.35 V. Calibration plots are obtained for all three metals, individually and simultaneously, in the 10-100 microg L(-1) range, with a detection limit of 93, 54, and 396 ng L(-1) for Pb(II), Cd(II), Zn(II), respectively. A slight reduction in slope is observed for Cd(II) and Pb(II) when the three metals are calibrated simultaneously vs. individually. Comparing the sensitivities of the metals when calibrated individually vs. in a mixture reveals that Zn(II) is not affected by stripping in a mixture. However, Pb(II) and Cd(II) have decreasing sensitivities in a mixture. The optimized method has been successfully used to test contaminated river water by standard addition. The results demonstrate the ability of the BiBE as an alternative electrode material in heavy metal analysis.

Optical fluorescence sol-gel sensors have been developed for the detection of carbon dioxide gas in the 0.03-30% range with a detection limit of 0.008% (or 80 ppm) and a quantitation limit of 0.02% (or 200 ppm) CO(2). Sol-gels were spin-coated on glass slides to create an organically modified silica-doped matrix with the 1-hydroxypyrene-3,6,8-trisulfonate (HPTS) fluorescent indicator. The luminescence intensity of the HPTS indicator (513 nm) is quenched by CO(2), which protonates the anionic form of HPTS. An ion pair technique was used to incorporate the lipophilic dye into the hydrophilic sol-gel matrix. TiO(2) particles (5 microm diameter) were added to induce Mie scattering and increase the incident light interaction with the sensing film, thus increasing the signal-to-noise ratio. Moisture-proof overcoatings have been used to maintain a constant level of water inside the sensor films. The optical sensors are inexpensive to prepare and can be easily coupled to fiber optics for remote sensing capabilities. A fiber-optic bundle was used for the gas detection and shown to work as part of a multianalyte platform for simultaneous detection of multiple analytes. The studies reported here resulted in the development of sol-gel optical fluorescent sensors for CO(2) gas with sensitivity below that in the atmosphere (ca. 387 ppm). These sensors are a complementary approach to current FT-IR measurements for real-time carbon dioxide detection in environmental applications.

The use of sol-gels as a sensing matrix for the development of unique sensing strategies is discussed. Sol-gels offer almost limitless possibilities for sensing substrates due to the variety of physical properties that can be obtained by altering a number of discussed fabrication conditions and techniques. By careful consideration of the sensing requirements, novel detection methods have been developed for a variety of analytes and applications. Here, sol-gels have been used to monitor pH at the extreme ends of the scale ([H+] = 1–11 M and [OH−] = 1–10 M) and in mixed solvent/solute systems using dual sensing approaches. The use of ligand-grafted sol-gel monoliths for optical determination of metal ion species is also discussed. The electrochemical determination of Cr(VI) by electrodeposited sol-gel modified electrodes is also presented.

Moisture and contaminant transport in partially saturated, heterogeneous, layered sediments is typically anisotropic. Solute transport parameters, including dispersivity and the adsorption coefficient, and the modeled concentration of reactive minerals may depend on the direction of flow with respect to sedimentary layering. Reaction rates, in contrast, should be independent of flow direction. We determined the influence of flow direction on transport parameters for nonreactive (Br{sup -}) and reactive (cobalt ethylenediaminetetraacetic acid [Co(II)EDTA{sup 2-}]) solutes under partially saturated conditions by imposing flow either parallel to or across sedimentary bedding in 11 intact sediment cores of various textures. Higher dispersivity of nonreactive tracers in parallel-bed cores suggested fluid channeling through permeable layers, while low-conductivity layers dampened channeling in cross-bed samples. Rates of transformation of Co(II)EDTA{sup 2-} into Co(III)EDTA{sup -} and of disassociation of Co{sup 2+} and EDTA{sup 4-} were modeled assuming that the reaction rates were independent of the flow direction. The concentration of Mn oxides that was responsible for the transformation reaction was dependent on the flow direction, which governed the extent of contact between the solution and the solid phase. Similarly, the adsorption constants of Co(II)EDTA{sup 2-} and Co(III)EDTA{sup -} were dependent on the flow direction but were also unique formore » each experiment. The modeled concentration of reactive minerals was the most sensitive parameter describing the reaction and transformation of Co(II)EDTA{sup 2-}.« less

An electrochemical technique has been developed for ultra-trace (ng L −1 ) vanadium (V) measurement. Catalytic adsorptive stripping voltammetry for V analysis was developed at mercury-coated gold micro-wire electrodes (MWEs, 100 μm) in the presence of gallic acid (GA) and bromate ion. A potential of −0.275 V (vs Ag/AgCl) was used to accumulate the complex in acetate buffer (pH 5.0) at the electrode surface followed by a differential pulse voltammetric scan. Parameters affecting the electrochemical response, including pH, concentration of GA and bromate, deposition potential and time have been optimized. Linear response was obtained in the 0–1000 ng L −1 range (2 min deposition), with a detection limit of 0.88 ng L −1 . The method was validated by comparison of results for an unknown solution of V by atomic absorption measurement. The protocol was evaluated in a real sample by measuring the amount of V in river water samples. Thick bismuth film electrodes with protective polystyrene films have also been made and evaluated as a mercury free alternative. However, ng L −1 level detection was only attainable with extended (10 min) deposition times. The proposed use of MWEs for the detection of V is sensitive enough for future use to test V concentration in biological fluids treated by the advanced oxidation process (AOP).

The LANDSAT Signature Development Program, LSDP, is designed to produce an unsupervised classification of a scene from a LANDSAT tape. This classification is based on the clustering tendencies of the multispectral scanner data processed from the scene. The program will generate a character map that, by identifying each of the general classes of surface features extracted from the scene data with a specific line printer symbols, indicates the approximate locations and distributions of these general classes within the scene. Also provided with the character map are a number of tables each of which describes either some aspect of the spectral properties of the resultant classes, some inter-class relationship, the incidence of picture elements assigned to the various classes in the character map classification of the scene, or some significant intermediate stage in the development of the final classes.