Biomedical subjects
SV Pisupati
Publications and source records attributed to SV Pisupati.
Partitioning behavior of trace elements during pilot-scale combustion of pulverized coal and coal-water slurry fuel
Release pathways for inorganic hazardous air pollutants (IHAPs) from a pilot-scale, down-fired combustor (DFC) when firing pulverized coal (PC) and coal-water slurry fuel (CWSF) were identified and quantified to demonstrate the effect of fuel form on IHAP partitioning, enrichment and emissions. The baghouse capturing efficiency for each element was calculated to determine the effectiveness of IHAP emission control. Most of the IHAPs were enriched in the fly ash and depleted in the bottom ash. Mercury was found to be enriched in the flue gas, and preferentially emitted in the vapor phase. When firing CWSF, more IHAPs were partitioned in the bottom ash than when firing PC. Significant reduction of Hg emissions during CWSF combustion was also observed.
An investigation on polycyclic aromatic hydrocarbon emissions from pulverized coal combustion systems
Results from a series of tests conducted to study the emission of polynuclear or polycyclic aromatic hydrocarbons (PAHs) from bench-scale and small industrial, water-tube boiler are discussed. A Middle Kittanning, and Upper Freeport seam coals were used in the study. Samples were extracted from the reactor outlet and from the inlet and outlet sides of the research boiler's (RB) baghouse using EPA promulgated methods.Only acenaphthene and fluoranthene were detected in down-fired combustor (DFC) samples. In addition to these two, naphthalene was detected in the RB samples. Emission factors ranged from 80 to 320 &mgr;g/kg of fuel fired. Although there were minor trends in the emissions' data, given the reproducibility limits for PAH compounds, no significant differences were found in the emissions with respect to the fuel type or form (pulverized coal (PC) vs. coal-water slurry fuel (CWSF), and raw vs. cleaned coal) and firing conditions (high and low excess air). The PAH emissions showed a decrease with increase in the firing rate.A bench-scale drop-tube reactor (DTR) was used to study the effects of temperature and residence time on PAH formation. The results revealed near constant PAH concentrations in the solid-phase samples, while the PAH concentrations in the vapor-phase samples increased as a function of temperature. At a temperature of around 1300 degrees C, the rate of PAH formation was exceeded by the rate of PAH oxidation, and PAH concentrations in the vapor phase began to decrease.