Spectrophotometric Method for the Determination of Atmospheric Cr Pollution as a Factor to Accelerated Corrosion.

The effect of Cr(VI) pollution on the corrosion rate of corrugated iron roof samples collected from tanning industry areas was investigated through simulated laboratory exposure and spectrophotometric detection of Cr(III) deposit as a product of the reaction. The total level of Cr detected in the samples ranged from 113.892 ± 0.17 ppm to 53.05 ± 0.243 ppm and showed increasing trend as sampling sites get closer to the tannery and in the direction of tannery effluent stream. The laboratory exposure of a newly manufactured material to a simulated condition showed a relatively faster corrosion rate in the presence of Cr(VI) with concomitant deposition of Cr(III) under pH control. A significant (P = 0.05) increase in the corrosion rate was also recorded when exposing scratched or stress cracked samples. A coupled redox process where Cr(VI) is reduced to a stable, immobile, and insoluble Cr(III) accompanying corrosion of the iron is proposed as a possible mechanism leading to the elevated deposition of the latter on the materials. In conclusion, the increased deposits of Cr detected in the corrugated iron roof samples collected from tanning industry zones suggested possible atmospheric Cr pollution as a factor to the accelerated corrosion of the materials.

Fungal infection and aflatoxin contamination in maize collected from Gedeo zone, Ethiopia.

Aflatoxins contamination of maize exhibits a serious threat to human and animal health over the past few decades. To protect the safety of food commodities, regular monitoring for afltoxins in food is necessary. In the proposed study, we have followed a rapid and sensitive biosensor approach as well as thin layer chromatography method for quantification of aflatoxins. Our data demonstrate that all the samples tested were beyond the safety level of aflatoxins as determined by Food and Drug Administration and European Union. Results of fungal mycoflora evidenced the massive presence of Aspergillus species (75 %) followed by Fusarium (11 %), Penicillium (8 %) and Trichoderma (6 %) as characterized by biochemical and sporulation properties. Use of internationally developed biosensor for detection of fungal toxin in this work is the first approach that was utilized in the developing country like Ethiopia. In the end, we conclude that fungal contaminant and there metabolites are potential threat to the agricultural industry and require urgent intervention.

Determination of Spatial Chromium Contamination of the Environment around Industrial Zones.

This study was conducted to determine the spatial levels of chromium contamination of water, agricultural soil, and vegetables in the leather tanning industrial areas using spectrophotometric methods. The results showed elevated accumulation of total Cr ranging from 10.85 ± 0.885 mg/L to 39.696 ± 0.326 mg/L, 16.225 ± 0.12 mg/Kg to 1581.667 ± 0.122 mg/Kg, and 1.0758 ± 0.05348 mg/Kg to 11.75 ± 0.206 mg/Kg in water, agricultural soil, and vegetable samples, respectively. The highest levels of chromium (VI) found from the speciation study were 2.23 ± 0.032 mg/Kg and 0.322 ± 0.07 mg/L in soil and water samples, respectively, which decreased with distance from the tannery. Among the vegetables, the highest load of Cr(VI) was detected in onion root (0.048 ± 0.065 mg/Kg) and the lowest (0.004 ± 0.007 mg/Kg) in fruit of green pepper. The detected levels of Cr in all of the suggested samples were above the WHO permissible limits. The variations of the levels Cr(III) and Cr(VI) contamination of the environment with distance from the tannery were statistically significant (p = 0.05). Similarly, significant difference in the levels of Cr among the tested vegetables was recorded. The levels increased with decreasing distance from the effluent channel.

Eletrochemically actuated stop-go valves for capillary force-operated diagnostic microsystems.

Lateral-flow immunosensing devices continue to be the most successful commercial realization of analytical microdevices. They owe their success to their simplicity, which significantly depends on the capillary-driven flow and versatile technological platform that lends itself to fast and low-cost product development. To compete with such a convenient product, microsystems can benefit from simple-to-operate fluid manipulation. We show that the capillary-driven flow in microchannels can be manipulated with electrochemically activated valves with no moving parts. These valves consist of screen-printed electrode pairs that are transversal to the flow. One of the electrodes is solvent-etched to produce a superhydrophobic surface that provides passive stopping and facilitates low-voltage (~1 V) actuation of the flow via electrowetting. The operation of such valves in the stop-go mode, with a response time between 2 and 45 sec depending on the type and concentration of salt, is demonstrated. Mechanistic investigations indicated that the response depends on at least three phenomena that contribute to electrocapillarity: the electrochemical double-layer capacitance, specific counterion adsorption, and possible electrohydrodynamic effects.

Potentiometric online detection of aromatic hydrocarbons in aqueous phase using carbon nanotube-based sensors.

Surfaces made of entangled networks of single-walled carbon nanotubes (SWCNTs) display a strong adsorption affinity for aromatic hydrocarbons. Adsorption of these compounds onto the walls of SWCNTs changes the electrical characteristics of the SWCNT-solution interface. Using these features, we have developed a potentiometric sensor to detect neutral aromatic species. Specifically, we can detect online aromatic hydrocarbons in industrial coolant water. Our chromatographic results confirm the adsorption of toluene onto the walls of carbon nanotubes, and our impedance spectroscopy data show the change in the double layer capacitance of the carbon nanotube-solution interface upon addition of toluene, thus confirming the proposed sensing mechanism. The sensor showed a toluene concentration dependent EMF response that follows the shape of an adsorption isotherm and displayed an immediate response to the presence of toluene with a detection limit of 2.1 ppm. The sensor does not respond to other nonaromatic hydrocarbons that may coexist with aromatic hydrocarbons in water. It shows a qualitative sensitivity and selectivity of 100% and 83%, respectively, which confirms its ability to detect aromatic hydrocarbons in aqueous solutions. The sensor showed an excellent ability to immediately detect the presence of toluene in actual coolant water. Its operational characteristics, including its fast response, low cost, portability, and easy use in online industrial applications, improve those of current chromatographic or spectroscopic techniques.