Alemayehu Paulos Washe
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Research Subjects
Alemayehu Paulos Washe has a total of 25 co-authors. Here are the top co-authors by number of shared publications:
Bruno Teixeira-Dias
Univ Rovira & Virgili, Dept Chem Engn, Bioengn & Bioelectrochem Grp, E-43007 Tarragona, Spain
2 shared publicationsDereje Homa
Department of Chemistry, Hawassa University, P.O. Box 05, Hawassa, Ethiopia
2 shared publicationsDiego Bejarano-Nosas
Univ Rovira & Virgili, Dept Chem Engn, Bioengn & Bioelectrochem Grp, E-43007 Tarragona, Spain
2 shared publicationsErmias Haile
Department of Chemistry, Hawassa University, P.O. Box 05, Hawassa, Ethiopia
2 shared publicationsIoanis Katakis
Universitat Rovira i Virgili
2 shared publications- Ioanis Katakis
Department of Chemical Engineering, Universitat Rovira i Virgili, 43007 Tarragona, Spain
2 shared publications
Latest Publications
- Open Access
- 1 January 2021
- Published by Taylor & Francis in Sustainable Environment
- Vol. 7 (1)
Differential pulse voltammetric determination of hexavalent chromium using nickel hexacyanoferrate modified glassy carbon electrode
ABSRACT The current boom in the industrial sector of the country is arise scientific concern about environmental contamination by heavy metals such as chromium. The objective of this project is to fabricate a sensitive and selective electrode for differential pulse voltammetric determination of Cr (VI) in water samples and demonstrate its applicability in complex matrices such as tannery effluent. The drop casting method is use for electrode development. Experimental variables that can influence the DPV response of the developed electrode for Cr (VI) including strength of supporting electrolytes, pH of the solution, and concentration parameters were optimized. The figures of merit of the developed electrode were evaluated and the applicability was demonstrated through determination of Cr (VI) in tannery effluent water. The developed electrode was detected a very low level of Cr (VI) in acetate buffer at pH 5 with limit of detection and limit of quantification 0.0885 and 0.2950 μmol L−1, respectively. The linear calibration plot is R2 value of 0.999 suggesting a very good correlation between DPV current response and concentration of Cr (VI). The current electrode was simple to develop and can successfully be applied for the determination of Cr (VI) in wastewater samples.
- 1 January 2021
- Published by Taylor & Francis in Sustainable Environment
- Vol. 7 (1)
Open AccessDifferential pulse voltammetric determination of hexavalent chromium using nickel hexacyanoferrate modified glassy carbon electrode
ABSRACT The current boom in the industrial sector of the country is arise scientific concern about environmental contamination by heavy metals such as chromium. The objective of this project is to fabricate a sensitive and selective electrode for differential pulse voltammetric determination of Cr (VI) in water samples and demonstrate its applicability in complex matrices such as tannery effluent. The drop casting method is use for electrode development. Experimental variables that can influence the DPV response of the developed electrode for Cr (VI) including strength of supporting electrolytes, pH of the solution, and concentration parameters were optimized. The figures of merit of the developed electrode were evaluated and the applicability was demonstrated through determination of Cr (VI) in tannery effluent water. The developed electrode was detected a very low level of Cr (VI) in acetate buffer at pH 5 with limit of detection and limit of quantification 0.0885 and 0.2950 μmol L−1, respectively. The linear calibration plot is R2 value of 0.999 suggesting a very good correlation between DPV current response and concentration of Cr (VI). The current electrode was simple to develop and can successfully be applied for the determination of Cr (VI) in wastewater samples.
- Open Access
- 4 February 2019
- Published by Wiley in Journal of Food Quality
- Vol. 2019, 1-10
Use of Natural Dietary Spices for Reclamation of Food Quality Impairment by Aflatoxin
Certain natural dietary spices, in addition to their use in food flavoring and preservation, have the ability to detoxify or degrade a wide range of chemical carcinogens. In the present study, aqueous extracts of judiciously selected natural dietary spices were evaluated for their ability to degrade aflatoxin B1 (AFB1). A total of 9 spices including garlic (Allium sativum), ginger (Zingiber officinale), black cumin (Nigella sativum), clove (Syzygium aromaticum), sacred basil (Ocimum basilicum), lemon grass (Cymbopogon citratusL. (DC)Stapf)), thyme (Thymus schimperi), fenugreek (Trigonella foenum-graecum), and lemon traditionally used by the Ethiopian Community for food flavoring and preservation were considered. Aflatoxin degradation efficacy of the spice extracts was studied through determination of the toxin in extract-treated and nontreated samples using LC-MS/MS. The degradation was characterized by electrochemical methods based on the characteristic oxidation peak of phenolic hydroxyl resulting from the degradation of the toxin after treatment with the extracts. Of the various spices, garlic showed the highest 35.8% (30 min) to 61.7% (1 hr) in spiked and 46.7% (30 min) to 68.3% (1 hr) and real-sample (contaminated maize) treatment reduction followed by lemon 34.2% (30 min) to 56.0% (1 hr) in spiked and 41.1% (30 min) to 60.6% (1 hr) in real-sample treatment at 25°C. The level of reduction was higher in real-sample treatment than that in spiked. This suggests adsorptive contribution by the matrix in addition to the chemical degradation. The current findings revealed nonobvious benefits of the use of natural dietary spices as effective solution for AFB1 degradation and decontamination of food.
- 4 February 2019
- Published by Wiley in Journal of Food Quality
- Vol. 2019, 1-10
Open AccessUse of Natural Dietary Spices for Reclamation of Food Quality Impairment by Aflatoxin
Certain natural dietary spices, in addition to their use in food flavoring and preservation, have the ability to detoxify or degrade a wide range of chemical carcinogens. In the present study, aqueous extracts of judiciously selected natural dietary spices were evaluated for their ability to degrade aflatoxin B1 (AFB1). A total of 9 spices including garlic (Allium sativum), ginger (Zingiber officinale), black cumin (Nigella sativum), clove (Syzygium aromaticum), sacred basil (Ocimum basilicum), lemon grass (Cymbopogon citratusL. (DC)Stapf)), thyme (Thymus schimperi), fenugreek (Trigonella foenum-graecum), and lemon traditionally used by the Ethiopian Community for food flavoring and preservation were considered. Aflatoxin degradation efficacy of the spice extracts was studied through determination of the toxin in extract-treated and nontreated samples using LC-MS/MS. The degradation was characterized by electrochemical methods based on the characteristic oxidation peak of phenolic hydroxyl resulting from the degradation of the toxin after treatment with the extracts. Of the various spices, garlic showed the highest 35.8% (30 min) to 61.7% (1 hr) in spiked and 46.7% (30 min) to 68.3% (1 hr) and real-sample (contaminated maize) treatment reduction followed by lemon 34.2% (30 min) to 56.0% (1 hr) in spiked and 41.1% (30 min) to 60.6% (1 hr) in real-sample treatment at 25°C. The level of reduction was higher in real-sample treatment than that in spiked. This suggests adsorptive contribution by the matrix in addition to the chemical degradation. The current findings revealed nonobvious benefits of the use of natural dietary spices as effective solution for AFB1 degradation and decontamination of food.
- Open Access
- 3 February 2019
- Published by Wiley in International Journal of Electrochemistry
- Vol. 2019, 1-8
Voltammetric Determination of Uric Acid in Clinical Serum Samples Using DMF Modified Screen Printed Carbon Electrodes
Screen printed carbon electrodes (SPCEs) provide attractive opportunity for sensitive and selective determination target analytes in clinical samples. The aim of the current work was to develop SPCEs based sensor for the determination of uric acid in clinical serum samples. The electrodes were pretreated by soaking in N,N-dimethylformamide for 5 minutes followed by drying in an oven at 100°C for 20 mins. The effect of surface pretreatment was characterized using cyclic voltammetry. The current response of uric acid detection was improved by a factor of 3.5 in differential pulse voltammetric measurement compared to unmodified electrode. Under the optimized conditions, the sensor displayed two dynamic linear ranges 5-100 μM and 100-500 μM with correlation coefficient, R2, values of 0.98782 and 0.97876, respectively. The limit of detection and limit of quantification calculated using the dynamic linear range 5-100 μM were 1.9 x 10−7 M and 6.33 x 10−7 M, respectively. The developed sensor displayed well separated and discerned peaks for UA in presence of the potential interferent (ascorbic acid and citric acid). The electrode was successfully applied for the detection of very low level of UA in clinical serum samples in a phosphate buffer solution (pH = 7). The proposed sensor showed a very high reproducibility and repeatability with the relative standard deviation of 0.9%. In conclusion, a simple and low cost sensor based on SPCEs is developed for sensitive and selective detection of uric acid in clinical samples.
- 3 February 2019
- Published by Wiley in International Journal of Electrochemistry
- Vol. 2019, 1-8
Open AccessVoltammetric Determination of Uric Acid in Clinical Serum Samples Using DMF Modified Screen Printed Carbon Electrodes
Screen printed carbon electrodes (SPCEs) provide attractive opportunity for sensitive and selective determination target analytes in clinical samples. The aim of the current work was to develop SPCEs based sensor for the determination of uric acid in clinical serum samples. The electrodes were pretreated by soaking in N,N-dimethylformamide for 5 minutes followed by drying in an oven at 100°C for 20 mins. The effect of surface pretreatment was characterized using cyclic voltammetry. The current response of uric acid detection was improved by a factor of 3.5 in differential pulse voltammetric measurement compared to unmodified electrode. Under the optimized conditions, the sensor displayed two dynamic linear ranges 5-100 μM and 100-500 μM with correlation coefficient, R2, values of 0.98782 and 0.97876, respectively. The limit of detection and limit of quantification calculated using the dynamic linear range 5-100 μM were 1.9 x 10−7 M and 6.33 x 10−7 M, respectively. The developed sensor displayed well separated and discerned peaks for UA in presence of the potential interferent (ascorbic acid and citric acid). The electrode was successfully applied for the detection of very low level of UA in clinical serum samples in a phosphate buffer solution (pH = 7). The proposed sensor showed a very high reproducibility and repeatability with the relative standard deviation of 0.9%. In conclusion, a simple and low cost sensor based on SPCEs is developed for sensitive and selective detection of uric acid in clinical samples.
- Open Access
- 1 January 2018
- Published by Wiley in Journal of Food Quality
- Vol. 2018, 1-10
Reduction of Aflatoxin M1 Levels during Ethiopian Traditional Fermented Milk (Ergo) Production
In this study, the reduction of aflatoxin M1 (AFM1) levels during lab-scale ergo production was investigated through determination of the residual levels of AFM1 using Enzyme Linked Immunosorbent Assay. The results showed gradual and incubation time dependent reduction of AFM1 level in the raw milk samples being fermented to ergo. The maximum reductions of 57.33 and 54.04% were recorded in AFM1 in natural and LAB inoculums initiated fermentations, respectively, in 5 days of incubation. Although a significant difference () in the AFM1 decrease in the two types of fermentations was recorded, such findings could vary with milk samples depending on initial load of the microorganisms as determined by hygienic conditions. However, the level of AFM1 in control (sterilized) samples showed only a 5.5% decrease during the entire period of incubation. Microbiological investigation showed increasing LAB counts with incubation time. A gradual decrease in pH of the milk samples was observed during fermentation. Considering the fact that both viable and dead bacterial cells could remove AFM1 during ergo production, the mechanism is proposed as predominantly involving noncovalent binding of the toxin with the chemical components of the bacterial cell wall.- 1 January 2018
- Published by Wiley in Journal of Food Quality
- Vol. 2018, 1-10
Open AccessReduction of Aflatoxin M1 Levels during Ethiopian Traditional Fermented Milk (Ergo) Production
In this study, the reduction of aflatoxin M1 (AFM1) levels during lab-scale ergo production was investigated through determination of the residual levels of AFM1 using Enzyme Linked Immunosorbent Assay. The results showed gradual and incubation time dependent reduction of AFM1 level in the raw milk samples being fermented to ergo. The maximum reductions of 57.33 and 54.04% were recorded in AFM1 in natural and LAB inoculums initiated fermentations, respectively, in 5 days of incubation. Although a significant difference () in the AFM1 decrease in the two types of fermentations was recorded, such findings could vary with milk samples depending on initial load of the microorganisms as determined by hygienic conditions. However, the level of AFM1 in control (sterilized) samples showed only a 5.5% decrease during the entire period of incubation. Microbiological investigation showed increasing LAB counts with incubation time. A gradual decrease in pH of the milk samples was observed during fermentation. Considering the fact that both viable and dead bacterial cells could remove AFM1 during ergo production, the mechanism is proposed as predominantly involving noncovalent binding of the toxin with the chemical components of the bacterial cell wall. - Open Access
- 2 April 2017
- Published by Wiley in Journal of Analytical Methods in Chemistry
- Vol. 2017, 1-9
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 (= 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.- 2 April 2017
- Published by Wiley in Journal of Analytical Methods in Chemistry
- Vol. 2017, 1-9
Open AccessSpectrophotometric 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 (= 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. - Open Access
- 17 June 2016
- Published by Springer Nature in SpringerPlus
- Vol. 5 (1) , 753
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.
- 17 June 2016
- Published by Springer Nature in SpringerPlus
- Vol. 5 (1) , 753
Open AccessFungal 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.
- Open Access
- 10 January 2016
- Published by Sciencedomain International in British Journal of Pharmaceutical Research
- Vol. 10 (6) , 1-9
Hepatoprotective Activities and Bioactive Constituents of Stephania abyssinica
Aims: To evaluate the hepatoprotective activity of Stephania abyssinica (S. abyssinica) and isolate the bioactive constituents. Study Design: The in vivo hepatoprotective activity of the extracts was evaluated by measuring serum levels of biochemical parameters of liver function in carbon tetrachloride (CCl4) treated rats. Place and Duration of Study: A preliminary survey was conducted in the rural areas of Wolaita (Southern part of Ethiopia) from September to December 2015. Pharmacological and phytochemical studies were conducted at the Laboratories of Department of Pharmacology, and Department of Chemistry of Dilla University. Methodology: The in vivo hepatoprotective activity of methanolic extracts of roots and rhizomes of the plant was studied by determining serum levels of the biochemical markers of liver function including glutamate oxaloacetate transaminase (GOT), glutamate pyruvate transaminase (GPT), alkaline phosphatase (ALP), total protein, and bilirubin concentrations before and after treatments with CCl4 and plant extracts. Bioactive principles were isolated by fractionation followed by concentration by preparative Thin Layer Chromatography. The structures of the compounds were elucidated using spectroscopic techniques including 1H NMR, 13CNMR, DEPT-135, 1H-1H COSY, HMQC and HMBC. Results: Administration of CCl4 alone to the rats significantly increased the total bilirubin concentration, GOT, GPT, and ALP (P = 0.05). However, simultaneous injection of oral dose of 200 mg/kg b.wt of the extracts reduced the serum levels of the enzymes by 53.42, 33.62, and 55.00% respectively. When 100 mg/Kg b.wt standard drug Silymarin was used, the decrease in the enzyme levels was by 44.00, 66.84, and 58.36%. Our fractionation experiments led to the identification of new hasubanan type alkaloid named as 6-(3’-hydroxy-4’-methoxycinnamoyl) stephine and the containing fraction displayed moderate hepatoprotective activity. Conclusions: The observed hepatoprotective activities of methanolic extracts of roots and rhizomes of S. abyssinica lend credence to its claimed traditional use against liver diseases.
- 10 January 2016
- Published by Sciencedomain International in British Journal of Pharmaceutical Research
- Vol. 10 (6) , 1-9
Open AccessHepatoprotective Activities and Bioactive Constituents of Stephania abyssinica
Aims: To evaluate the hepatoprotective activity of Stephania abyssinica (S. abyssinica) and isolate the bioactive constituents. Study Design: The in vivo hepatoprotective activity of the extracts was evaluated by measuring serum levels of biochemical parameters of liver function in carbon tetrachloride (CCl4) treated rats. Place and Duration of Study: A preliminary survey was conducted in the rural areas of Wolaita (Southern part of Ethiopia) from September to December 2015. Pharmacological and phytochemical studies were conducted at the Laboratories of Department of Pharmacology, and Department of Chemistry of Dilla University. Methodology: The in vivo hepatoprotective activity of methanolic extracts of roots and rhizomes of the plant was studied by determining serum levels of the biochemical markers of liver function including glutamate oxaloacetate transaminase (GOT), glutamate pyruvate transaminase (GPT), alkaline phosphatase (ALP), total protein, and bilirubin concentrations before and after treatments with CCl4 and plant extracts. Bioactive principles were isolated by fractionation followed by concentration by preparative Thin Layer Chromatography. The structures of the compounds were elucidated using spectroscopic techniques including 1H NMR, 13CNMR, DEPT-135, 1H-1H COSY, HMQC and HMBC. Results: Administration of CCl4 alone to the rats significantly increased the total bilirubin concentration, GOT, GPT, and ALP (P = 0.05). However, simultaneous injection of oral dose of 200 mg/kg b.wt of the extracts reduced the serum levels of the enzymes by 53.42, 33.62, and 55.00% respectively. When 100 mg/Kg b.wt standard drug Silymarin was used, the decrease in the enzyme levels was by 44.00, 66.84, and 58.36%. Our fractionation experiments led to the identification of new hasubanan type alkaloid named as 6-(3’-hydroxy-4’-methoxycinnamoyl) stephine and the containing fraction displayed moderate hepatoprotective activity. Conclusions: The observed hepatoprotective activities of methanolic extracts of roots and rhizomes of S. abyssinica lend credence to its claimed traditional use against liver diseases.
- Open Access
- 10 January 2016
- Published by Sciencedomain International in British Journal of Applied Science & Technology
- Vol. 15 (1) , 1-8
Instrumental Approach to the Determination of Ozone Phytotoxicity
Ozone (O3) phytotoxicity is a serious concern all over the globe. O3 can cause both biochemical and physiological changes to plants that could lead to reduction in growth and yield. Its effect on agricultural crops is usually detected as foliar injury. Although foliar injury has frequently served as physiological basis for monitoring performance of agricultural crops and assessing air quality, its visibility depends on period of exposure, concentration of ozone, and environmental conditions. The present study focused on the determination of biochemical indicators of ozone phytotoxicity including Rubisco (biochemical indicator for carbon assimilation), photo-pigments [carotenoids and chlorophyll (a & b)], and chlorophyll photochemical efficiency on a judiciously selected plant-Nicotiana tabacum (Tobacco), variety: Little Havanna. An enclosed computer controlled growth chamber was used for cultivation of the experimental plant groups (ozone exposed and control). Spectrophotometric measurements of the biochemical indicators were carried out to evaluate the exposure-response behaviour of the plant. Our results showed a significant (P< 0.05) decrease of the biochemical indicators that is reproducible even when foliar injury is not detected. Besides, experiments also showed that chlorophyll a is more sensitive to ozone than chlorophyll b. The instrumental readings were supported by a reduction in total organic nitrogen and starch content and ultimate decrease in growth rate and root: shoot ratio. While significant variations in the intensities of foliar injury can be detected among plants within a group, a reproducible exposure-response data were obtained from instrumental measurements. Such measurements can also serve as basis for the development of implantable sensors for in-situ monitoring of ozone pollution in sensitive crops.
- 10 January 2016
- Published by Sciencedomain International in British Journal of Applied Science & Technology
- Vol. 15 (1) , 1-8
Open AccessInstrumental Approach to the Determination of Ozone Phytotoxicity
Ozone (O3) phytotoxicity is a serious concern all over the globe. O3 can cause both biochemical and physiological changes to plants that could lead to reduction in growth and yield. Its effect on agricultural crops is usually detected as foliar injury. Although foliar injury has frequently served as physiological basis for monitoring performance of agricultural crops and assessing air quality, its visibility depends on period of exposure, concentration of ozone, and environmental conditions. The present study focused on the determination of biochemical indicators of ozone phytotoxicity including Rubisco (biochemical indicator for carbon assimilation), photo-pigments [carotenoids and chlorophyll (a & b)], and chlorophyll photochemical efficiency on a judiciously selected plant-Nicotiana tabacum (Tobacco), variety: Little Havanna. An enclosed computer controlled growth chamber was used for cultivation of the experimental plant groups (ozone exposed and control). Spectrophotometric measurements of the biochemical indicators were carried out to evaluate the exposure-response behaviour of the plant. Our results showed a significant (P< 0.05) decrease of the biochemical indicators that is reproducible even when foliar injury is not detected. Besides, experiments also showed that chlorophyll a is more sensitive to ozone than chlorophyll b. The instrumental readings were supported by a reduction in total organic nitrogen and starch content and ultimate decrease in growth rate and root: shoot ratio. While significant variations in the intensities of foliar injury can be detected among plants within a group, a reproducible exposure-response data were obtained from instrumental measurements. Such measurements can also serve as basis for the development of implantable sensors for in-situ monitoring of ozone pollution in sensitive crops.
- Open Access
- 1 January 2016
- Published by Wiley in International Journal of Analytical Chemistry
- Vol. 2016, 1-7
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 mg/L to mg/L, mg/Kg to mg/Kg, and mg/Kg to mg/Kg in water, agricultural soil, and vegetable samples, respectively. The highest levels of chromium (VI) found from the speciation study were mg/Kg and 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 ( mg/Kg) and the lowest ( 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 (). Similarly, significant difference in the levels of Cr among the tested vegetables was recorded. The levels increased with decreasing distance from the effluent channel.- 1 January 2016
- Published by Wiley in International Journal of Analytical Chemistry
- Vol. 2016, 1-7
Open AccessDetermination 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 mg/L to mg/L, mg/Kg to mg/Kg, and mg/Kg to mg/Kg in water, agricultural soil, and vegetable samples, respectively. The highest levels of chromium (VI) found from the speciation study were mg/Kg and 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 ( mg/Kg) and the lowest ( 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 (). Similarly, significant difference in the levels of Cr among the tested vegetables was recorded. The levels increased with decreasing distance from the effluent channel. - 1 November 2013
- Published by Elsevier in Microelectronic Engineering
- Vol. 111, 416-420
Electrochemically actuated passive stop–go microvalves for flow control in microfluidic systems
- 1 November 2013
- Published by Elsevier in Microelectronic Engineering
- Vol. 111, 416-420
Electrochemically actuated passive stop–go microvalves for flow control in microfluidic systems