Investigation of Selective Catalytic Reduction Impact on Mercury Speciation under Simulated NOx Emission Control Conditions

Abstract

Selective catalytic reduction (SCR) technology increasingly is being applied for controlling emissions of nitrogen oxides (NO_x) from coal-fired boilers. Some recent field and pilot studies suggest that the operation of SCR could affect the chemical form of mercury (Hg) in coal combustion flue gases. The speciation of Hg is an important factor influencing the control and environmental fate of Hg emissions from coal combustion. The vanadium and titanium oxides, used commonly in the vanadia-titania SCR catalyst for catalytic NO_x reduction, promote the formation of oxidized mercury (Hg²⁺).

The work reported in this paper focuses on the impact of SCR on elemental mercury (Hg⁰) oxidation. Bench-scale experiments were conducted to investigate Hg⁰ oxidation in the presence of simulated coal combustion flue gases and under SCR reaction conditions. Flue gas mixtures with different concentrations of hydrogen chloride (HCl) and sulfur dioxide (SO₂) for simulating the combustion of bituminous coals and subbituminous coals were tested in these experiments. The effects of HCl and SO₂ in the flue gases on Hg⁰ oxidation under SCR reaction conditions were studied. It was observed that HCl is the most critical flue gas component that causes conversion of Hg⁰ to Hg²⁺ under SCR reaction conditions. The importance of HCl for Hg⁰ oxidation found in the present study provides the scientific basis for the apparent coal-type dependence observed for Hg⁰ oxidation occurring across the SCR reactors in the field.     

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.     

Characterization and pollutant removal efficiency of biochar derived from baggase,bamboo and tyre

Conversion of broad-spectrum organic waste into carbonaceous biochar has gained enormous interest in past few years. The present study aims to characterize feedstock (FS), i.e. bagasse (Bg), bamboo (Bm) and biochar (BC), i.e. baggase biochar (BBg), bamboo biochar (BBm) and tyre biochar (Ty). Significant changes in elemental composition, atomic ratio, proximate analyses, mineral content and heavy metal content were observed which was well supported by Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) analysis. Impregnation with ferric hydroxide was done, and resultant modified biochars (MBC), i.e. iron-impregnated baggase biochar (FeBBg), iron-impregnated bamboo biochar (FeBBm) and iron-impregnated tyre biochar (FeTy), along feedstock and biochar were used for PO₄ ^3?, Pb, Hg and Cu adsorption. In general, BBg, FeBBg, BBm, FeBBm, Ty and FeTy were found to adsorb PO₄ ^3?, Pb, Hg and Cu better than Bg and Bm, except in few cases. Results from adsorption experiments were fitted into Langmuir, Freundlich and Temkin models of isotherms and pseudo-first-order, pseudo-second-order and Elovich models of kinetics. Result of batch study adsorption revealed that maximum adsorption of PO₄ ^3?, Pb, Hg and Cu was done by FeBBg (adsorption mechanism explained by Freundlich model), FeTy (Temkin model), Ty (Langmuir model) and BBm (Langmuir model) respectively. According to R ² values, pseudo-first-order reaction was well suited to PO₄ ^3?, Pb, Hg and Cu adsorption. The optimum pH for maximum adsorption was observed to be 7.4 for PO₄ ^3?, 5 for Cu and 6 for Pb and Hg respectively     

Impact of different types of polluted irrigation water on soil fertility and wheat grain yield in clayey black soils of central India

This study was carried out in three different cities of western Madhya Pradesh (India) to investigate the effects of long-term irrigation with industrial waste water (IWW), contaminated groundwater (CGW), and untreated municipal sewage water (USW) on soil fertility as well as on wheat crop yield. Irrigation with these three types of polluted water increased organic matter content as well as contents of available P (with IWW and USW only), available K, available S, available Zn, available Cu (IWW only), and available Mn (IWW and CGW only). The magnitude of improvement in soil fertility status was the highest in the case of USW, followed by IWW and finally, by CGW. Concentrations of Na in wheat leaf tissue increased by 198 and 58 % whereas concentrations of Ca decreased significantly by 16 and 13 % due to the use of IWW and CGW, respectively, resulting in poor Ca nutrition to the crop. Although wheat grain yield increased considerably due to USW, the same recorded significant decreases with IWW and CGW. In spite of the enhancement in the available nutrient status, decrease in wheat grain yield with the use of IWW and CGW could be due to the build-up of salts in the soil and an imbalance in the Na/Ca ratio in wheat crops irrigated with IWW and CGW. The adverse effect on wheat productivity was more pronounced with IWW as compared to CGW.     

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.     

Arsenic occurrence and accumulation in soil and water of eastern districts of Uttar Pradesh, India

Arsenic in the soil and water of eastern districts of Uttar Pradesh (Ballia and Ghazipur) was estimated. Survey results revealed that arsenic in soil samples ranged from 5.40 to 15.43 parts per million (ppm). In water samples, it ranged from 43.75 to 620.75 parts per billion (ppb) which far exceeded the permissible limit of 10 ppb as recommended by the World Health Organization. Maximum concentration of arsenic in water was found in Haldi village of Ballia (620.75 ppb). However, mean arsenic concentration in water followed the order: Karkatpur (257.21 ppb) < Haldi (310.15 ppb) < Sohaon (346.94 ppb) < Dharmarpur (401.75 ppb). In case of soil, maximum arsenic was detected in soil of Sohaon (15.43 ppm). Mean arsenic levels in soils followed the order: Karkatpur (9.24 ppm) < Haldi (9.82 ppm) < Dharmarpur (11.32 ppm) < Sohaon (14.08 ppm). Arsenic levels were higher in soils collected from 15–30 cm depth than 0–15 cm from the soil surface.     

The effects of meteorological parameters in ambient noise modelling studies in Delhi

The acoustic environment in urban areas has gained prominence in recent times due to rapid industrial and commercial development in metropolitan cities. Various attempts have been made to predict and model the trends in urban ambient noise levels using different statistical and dynamic models. The present study makes an attempt to examine the role of meteorological parameters affecting the ambient noise levels in Delhi. The results show significant improvement in overall noise scenario of Delhi since the introduction of compressed natural gas vehicles in public transport of Delhi. The noise level is significantly reduced by high vegetation cover as well as by low relative humidity over Delhi. The regression models developed for the present study clearly show the significant contribution of meteorological parameters in governing the ambient noise levels in Delhi.     

Development and demonstration of a free surface flow-dependent sampling technology

Statistical assessment of water quality data, obtained at the South Florida Water Management District (West Palm Beach, Florida) S-65E structure, illustrated significant differences and inconsistency in nutrient concentrations (Daas and Ebadian, 2003). The evaluation showed that currently used water sampling techniques are inadequate because of deficiencies in functionality and sensitivity to flow conditions at the structure. Moreover, the study indicated the need for a more precise sampling technology, which would consider variations in the velocity profile across the water column during the sampling process. Therefore, a new prototype sampling technology was designed and tested in a pilot open channel. The new sampler had the capability to collect discrete aliquot volumes of water samples that are proportional to the corresponding point velocity at each of these depths. The discrete aliquot volumes were blended to provide an integrated sample that captures the variations in the velocity profile.     

Modeling of 2-chloronaphthalene interaction with high carbon iron filings (HCIF) in semi-batch and continuous systems

Unrusted high carbon iron filings (HCIF) were contacted sequentially with successive aliquots of aqueous 2-chloronaphthalene (2-CN), i.e., in semi-batch mode, both in well-mixed and poorly-mixed conditions. Aqueous concentration of 2-CN and the dehalogenation by-product naphthalene (N) were monitored at the beginning and end of each 2-CN addition cycle. Experimental data was modeled using the 2-CN dehalogenation and adsorption/desorption rate constants determined from batch experiments involving 2-CN and a similar HCIF sample. Model predictions for the semi-batch experiments matched quite well with the experimental data in both well-mixed and poorly-mixed cases. Further, it was experimentally demonstrated that adsorption and hence accumulation of N on HCIF surface did not substantially hinder either 2-CN adsorption or dehalogenation under the conditions examined in this study. Continuous transport of water containing 0.5 μmol L^?1 2-CN through a 1.0-m thick unrusted HCIF layer was simulated at superficial velocities of 0.01 and 0.10 m h^?1. Both simulations indicated nearly complete removal of 2-CN in the HCIF layer. This study suggests that HCIF can be used as a potential reactive material in permeable reactive barriers (PRBs) for in situ remediation of groundwater contaminated with 2-CN.