Alumina-supported oxime for the degradation of sarin and diethylchlorophosphate

1-(4-Chlorophenyl))-N-hydroxymethanimine and cyclohexyl-N-hydroxymethanimine were synthesized and a well-established oxime, i.e., 2-[(hydroxyimino)methyl]-1-methylpyridinium chloride was purchased. Thereafter; all were loaded over Al₂O₃ using incipient wetness technique. The prepared systems were characterized using surface area analyzer, scanning electron microscope, energy dispersive X-ray spectrophotometer, Fourier transform infrared spectrophotometer and thermogravimetric analyzer. Kinetics of the degradation of sarin (GB) and simulant, i.e. diethylchlorophosphate (DEClP) was studied over synthesized oxime impregnated Al₂O₃ and results were compared with well reported oxime impregnated Al₂O₃. Kinetics of reaction was found to be following the pseudo first order reaction kinetics. The order of reactivity of the prepared systems was found to be cyclohexyl-N-hydroxymethanimine/Al₂O₃ > 1-(4-chlorophenyl)-N-hydroxymethanimine/Al₂O₃ > 2-[(hydroxyimino)methyl]-1-methylpyridinium chloride/Al₂O₃ > Al₂O₃. From the reaction kinetics it was observed that the reaction with DEClP was faster than with GB. Cyclohexyl-N-hydroxymethanimine/Al₂O₃ was found to be the most reactive system with half-life of 0.94 and 15 h for DEClP and GB respectively.     

Determination of sulfosulfuron residues in soil under wheat crop by a novel and cost-effective method and evaluation of its carryover effect

A novel and cost-effective method of sulfosulfuron extraction has been developed using distilled water as an extraction solvent. Using this method, the environmental fate of sulfosulfuron was investigated in soil under wheat crop. Studies were conducted under natural field conditions in randomized block design and herbicide (75% water dispersible granules (WG)) was applied after 24 days of sowing. The rates of applications were 25 and 50 g of active ingredient (a.i.) per hectare. Soil samples were collected at predetermined intervals and analyzed by high performance liquid chromatography (HPLC). The minimum detection limit was found to be 0.001 μ g g^{? 1}. The dissipation of sulfosulfuron followed first-order rate kinetics and dissipated with a half-life of 5.4–6.3 days. After harvest, field soil was used for conducting a pot experiment with bottle gourd (Lagenaria siceraria) as test plants to study the carry over effect of sulfosulfuron. No phytotoxicity was observed to bottle gourd in pot experiment with harvest soil.     

Persistence of hexaconazole,a triazole fungicide in soils

Abstract

Persistence of hexaconazole (2‐(2,4‐dichlorophenyl)‐l‐(lH‐l,2,5‐triazol‐l‐yl) hexan‐2‐ol) was studied in alluvial, red and black soils under flooded and nonflooded conditions. This fungicide was more persistent in all soils under flooded conditions than under nonflooded conditions and at 27°C than at 35°C. Degradation of hexaconazole in sterilized and nonsterilized soils proceeded at identical rates indicating a minor role of micro‐organisms in its degradation. The soil persistence of hexaconazole was not affected by the addition of wheat straw both under flooded and nonflooded conditions.     

Effect of UV radiation and temperature on mineralization and volatilization of coumaphos in water

This study was undertaken to determine the dissipation and degradation of coumaphos [O-(3-chloro-4-methyl-2-oxo-2H-1-benzopyran-7-yl) O,O-diethyl phosphorothioate] under different sunlight conditions and at different temperatures. The effect of the ultra violet (UV) component of solar radiation was also studied using quartz tubes in addition to other radiation in the visible range using glass tubes and the results were compared with those obtained under the dark light conditions. Water suspensions of coumaphos were incubated at three temperatures viz. 22 degrees C, 37 degrees C and 53 degrees C in closed systems to study the effect of temperature. Volatilization, mineralization and degradation of coumaphos increased with an increase in temperature and exposure to solar radiation, particularly under the UV component of the solar radiation. Major loss of the pesticide occurred through volatilization. The optimum temperature for the degradation of coumaphos was found to be at 37 degrees C. The data obtained from the mineralization and degradation studies indicated that 53 degrees C crosses the biological range for suitable growth of microorganism. UV radiation exposure along with maintaining temperature at 37 degrees C may prove useful in the dissipation and/or degradation of coumaphos prior to its disposal as waste from cattle dipping vats.     

House fly (Musca domestica): a review of control strategies for a challenging pest

Musca domestica L. (Diptera: Muscidae), commonly called the house fly, is a major domestic, medical and veterinary pest that causes irritation, spoils food and acts as a vector for many pathogenic organisms. In this paper, the social and health problems related to housefly are introduced with the associated need to control its population. Physical and chemical methods of house fly control are briefly discussed. The main focus of this review is on the biological control methods for house fly control, that comprise botanical, fungal, bacterial and parasitoid agents. Although several biocontrol agents are still in the nascent stage, some of them (especially fungal and parasitoid agents) have shown reliable field performance and seem to be suitable candidates for commercialization. However, the majority of these laboratory and field studies have been conducted in the temperate region. It remains to be seen whether the application of biocontrol agents would be feasible in tropical environments. The integrated pest management practices, which can provide more reliable field performance, have also been discussed. A multi-dimensional approach that exerts control on all the life stages of house fly, but simultaneously preserves the fly's natural enemies could be an ecologically sustainable way of maintaining the fly populations below maximally acceptable limits.     

The effect of temperature on PAHs emission from incineration of acrylic waste

Incineration of acrylic waste solution in a lab scale quartz tube vertical incinerator showed the presence of 12–15 polycyclic aromatic hydrocarbons (PAHs) from a list of 16 priority pollutants at 700–1100^˚C after an interval of 50^˚C. The amount of total 16 PAHs at 900 and 1100^˚C was about 8.5 and 1.25 times higher than those at 700^˚C (739.48 μg g⁻¹) respectively. The amount of total probable (2A) and possible (2B) human carcinogenic PAHs was minimum at 700^˚C.     

Efficacy of electrical resistivity and induced polarization methods for revealing fluoride contaminated groundwater in granite terrain

The accumulation of fluoride (F) in groundwater is a common phenomenon in India and worldwide. Its location can be identified through a direct hydrochemical analysis, which was carried out in Kurmapalli watershed (located 60 km SE of Hyderabad city), Nalgonda district, Andhra Pradesh, India affected by F contamination. The results of the hydrochemical analysis showed that F varied from 0.71 to 19.01 mg/l and its concentration exceeded the permissible limit (i.e., 1.5 mg/l) in 78% of the total 32 samples analyzed. The highest F value (19.01 mg/l) was found near Madnapur village, which is located in the central part of the watershed. Resistivity and induced polarization (IP) surveys were also carried out to reveal the zones where elevated F-contaminated groundwater exists. The objective of this paper was to highlight the utility of resistivity and IP surveys, using hydrochemical constituents as constraint, for the successful delineation of such contaminated/polluted groundwater zones in the granite area.     

Removal of hexavalent chromium from contaminated ground water using zero-valent iron nanoparticles

Batch experiments were conducted on ground water samples collected from a site contaminated with Cr(VI) to evaluate the redox potential of zero-valent iron (Fe⁰) nanoparticles for remediation of Cr(VI)-contaminated ground water. For this, various samples of contaminated ground water were allowed to react with various loadings of Fe⁰ nanoparticles for a reaction period of 60 min. Data showed 100% reduction of Cr(VI) in all the contaminated ground water samples after treatment with 0.20 gL⁻¹ of Fe⁰ nanoparticles. An increase in the reduction of Cr(VI) from 45% to 100% was noticed with the increase in the loading of Fe⁰ nanoparticles from 0.05 to 0.20 gL⁻¹. Reaction kinetics of Cr(VI) reduction showed pseudo first-order kinetics with rate constant in the range of 1.1 × 10⁻³ to 3.9 × 10⁻³ min⁻¹. This work demonstrates the potential utility of Fe⁰ nanoparticles in treatment and remediation of Cr(VI)-contaminated water source.     

Metal speciation studies in the aquifer sediments of Semria Ojhapatti,Bhojpur District,Bihar

The pollution of aquifer sediments by heavy metals has assumed serious concern due to their toxicity and accumulative behavior. Changes in environmental conditions can strongly influence the behavior of both essential and toxic elements by altering the forms in which they occur and therefore quantification of the different forms of metal is more meaningful than total metal concentrations. In this study, fractionation of metal ions in aquifer sediments of Semria Ojhapatti area, Bhojpur district, Bihar has been studied to determine the ecotoxic potential of metal ions. The investigations suggest that iron, copper, and arsenic have a tendency to remain associated in the following order residual > reducible > acid-soluble > oxidizable; manganese and zinc have tendency to be associated as residual > acid-soluble > reducible > oxidizable. The risk assessment code reveals that manganese and zinc occur in significant concentration in acid-soluble fraction and therefore comes under the high risk category and can easily enter the food chain. Most of the iron, copper, and arsenic occur as immobile fraction (i.e. residual) followed by its presence in reducible fraction and would pose threat to the water quality due to changing redox conditions. The metal enrichment factor in the study area shows moderate to significant metal enrichment in the aquifer sediments which may pose a real threat in near future. The geo-accumulation index of metals also shows that the metals lie in the range of strongly contaminated (for iron at shallow depths) to moderately contaminated to uncontaminated values.     

Carbon sequestration in reclaimed manganese mine land at Gumgaon, India

Carbon emission is supposed to be the strongest factor for global warming. Removing atmospheric carbon and storing it in the terrestrial biosphere is one of the cost-effective options, to compensate greenhouse gas emission. Millions of acres of abandoned mine land throughout the world, if restored and converted into vegetative land, would solve two major problems of global warming and generation of degraded wasteland. In this study, a manganese spoil dump at Gumgaon, Nagpur in India was reclaimed, using an integrated biotechnological approach (IBA). The physicochemical and microbiological status of the mine land improved after reclamation. Soil organic carbon (SOC) pool increased from 0.104% to 0.69% after 20 years of reclamation in 0–15 cm spoil depth. Soil organic carbon level of reclaimed site was also compared with a native forestland and agricultural land. Forest soil showed highest SOC level of 1.11% followed by reclaimed land and agriculture land of 0.70% and 0.40%, respectively. Soil profile studies of all three sites showed that SOC pool decreased from 0–15, 15–30, and 30–45 cm depths. Although reclaimed land showed less carbon than forestland, it showed better SOC accumulation rate. Reclamation of mine lands by using IBA is an effective method for mitigating CO₂ emissions.