Municipal Waste Combustion Abstracts
Sorption of Elemental Mercury by Activated Carbons
S.V. Krishnan Acurex Environmental Corporation 4915 Prospectus Drive P.O. Box 13109 Research Triangle Park, NC 27709 Brian K. Gullett U.S. Environmental Protection Agency Air and Energy Engineering Research Laboratory Research Triangle Park, NC 27711 Wojciech Jozewicz Acurex Environmental Corporation 4915 Prospectus Drive P.O. Box 13109 Research Triangle Park, NC 27709
Abstract
The mechanisms and rate of elemental mercury (Hgx) capture by activated
carbons have been studied using a bench-scale apparatus. Three types
of activated carbons, two of which are thermally activated (PC-100
and FGD) and one with elemental sulfur (S) impregnated in it (HGR),
were chosen to study the effects of surface area (approximately 550-1000
m2/g), sorption temperature (23 to 140 °C), and Hgx
concentration (30 and 60 ppb of Hgx in nitrogen). Investigations revealed
that sorption occurs in active sites in PC-100 and FGD which are either
depleted or deactivated upon heat treatment at 140 °C. For HGR,
sorption at 23 °C occurred in non-S sites residing in the external
surface and sorption at 140 °C primarily occurred through the
reaction of Hgx and S. Desorption studies for PC-100 and HGR revealed
the sorption mechanism to be a combination of physisorption and chemisorption
at 23 °C, whereas chemisorption is the primary route at 140 °C.
Gullett, B. K.; Jozewicz,
W.; and Stefanski, L. A. Reaction Kinetics of Ca-Based Sorbents with
HCl, Ind. & Eng. Chem. Res., 31(11), 2437-2446, 1992.
Reaction Kinetics of Ca-Based Sorbents with HCl
Brian K. Gullett Air and Energy Engineering Research Laboratory U.S. Environmental Protection Agency Research Triangle Park, NC 27711 Wojciech Jozewicz Acurex Environmental Corporation 4915 Prospectus Drive P.O. Box 13109 Research Triangle Park, NC 27709 Leonard A. Stefanski Department of Statistics North Carolina State University Raleigh, NC 27695
Abstract
The kinetics of the reaction between CaO and HCl were investigated under
conditions that minimize bulk mass transfer and pore diffusion limitations.
Reactivity data from 0.2- to 1-s exposure to 5000 ppm HCl in a fixed bed
reactor were analyzed by a shrinking core model of diffusion and chemical
reaction control, either singly or in combination. Between temperatures
of 150 and 350 °C, the reaction is controlled by gaseous diffusion
through the developing product layer. The apparent activation energy is
about 28.1 kJ/mol (6.7 kcal/mol), and the reaction is first order with
respect to HCl concentration. Reactivity is a minor function of the measured
particle size and surface area, likely due to the agglomerative nature
of the individual grains that comprise the particle structure and complicate
the interpretation of these measured values. Extrapolation of these results
to the high-temperature, furnace sorbent injection process provides preliminary
agreement with pilot-scale tests.
Paper presented at the 1993 International
Conference on Municipal Waste Combustion, March 30 - April 2, Williamsburgh,
VA.
Development of a Multifuel Combustor Research Facility
Chun Wai Lee Combustion Research Branch Air and Energy Engineering Research Laboratory U. S. Environmental Protection Agency Research Triangle Park, NC 27711
Abstract
A pilot-scale multifuel combustor (MFC) designed to permit research
with a variety of solid fuels is currently under development at EPA's
Air and Energy Engineering Research Laboratory (AEERL). The MFC is
designed with sufficient flexibility so that, with some minimum but
critical changes, it can be used for studying the combustion of municipal
solid waste (MSW), refuse derived fuel (RDF), biomass fuel, and coal.
Three interchangeable stoker grates are designed so the combustor
can be operated in spreader stoker, continuous mass burn, or batch
feed mass burn firing modes. The thermal output of the facility (580
kW) is sufficient to simulate the critical combustion conditions that
occur in full scale systems. The processes controlling pollutant formation
and destruction can be studied during combustion in the fuel bed,
in the radiant furnace, or in the convective section. The MFC facility
will also have the capability of studying the performance of flue
gas cleaning devices such as baghouses and scrubbers. After the combustion
conditions of the research unit are fully characterized, the initial
application of the facility will be focused on studying formation,
destruction, and control of pollutant emissions from MSW combustion
processes. The effects of waste stream composition, such as the type
and the quantity of paper, plastic, metal, and glass, on pollutant
emissions and their control will be evaluated.
Gullett, B. K.; Lemieux, P. M.; and
Dunn, J. E. The Role of Combustion and Sorbent Parameters in Prevention
of Polychlorinated Dibenzo-p-Dioxin and Polychlorinated Dibenzofuran
Formation During Waste Combustion, Environ. Sci. Technol. 28(1), 107-118,
1994.
The Role of Combusiton and Sorbent Parameters in Prevention of Polychlorinated Dibenzo-p-Dioxin and Polychlorinated Dibenzofuran Formation during Waste Combustion
Brian K. Gullett Paul M. Lemieux Air and Energy Engineering Research Laboratory U.S. Environmental Protection Agency Research Triangle Park, North Carolina 27711 and James E. Dunn Department of Mathematical Sciences University of Arkansas Fayetteville, Arkansas 72701
Abstract
This research uses experimental data and a statistical approach to
determine the effect of combustion- and sorbent-injection-related
parameters on the mechanism of polychlorinated dibenzo-p-dioxin
and polychlorinated dibenzofuran (PCDD and PCDF) formation and prevention
in waste combustors. The operation of a pilot-scale combustor was
varied to effect different regimes of oxygen (O2), hydrogen
chloride (HCl), and chlorine (Cl2) concentration; temperature;
residence time; quench rate; and sorbent injection. The fly ash loading
of a municipal waste combustor was simulated by post-combustion injection
of fly ash collected from a full-scale facility. Downstream sampling
and analysis indicated significant PCDD and PCDF formation, beyond
concentrations on the pre-injected fly ash, at rates conducive to
explaining formation in full-scale facilities at particle/gas residence
times 5 s. Stepwise regression analyses determined the predictive
parameters for four models of PCDD, PCDF, the total of PCDD and PCDF
yield, and the partitioning between PCDD and total yield. Substantial
prevention of PCDD and PCDF formation can be brought about with upstream
sorbent injection for HCl and Cl2 reduction, control of
excess air, and increased quench rate.
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