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Rachel K. La Fond John C. Kramlich Wm. Randall Seeker Gary S. Samuelsen 《Journal of the Air & Waste Management Association (1995)》2013,63(6):658-663
This paper discusses monitoring the waste destruction efficiency of hazardous waste incinerators. The particular problem is to ensure that incinerators do not release, without detection, significant quantities of waste as a result of operating fluctuations or equipment degradation. To detect these conditions, continuous, automated, and real-time source monitoring is required. Detection of degraded performance by monitoring and measuring waste compounds directly is not presently possible on a continuous basis. An alternative is to use commercially available continuous monitors to measure combustion intermediates (e.g., CO or hydrocarbons) and thereby infer waste destruction efficiency. Required, however, is a correlation between the emission of intermediates and the emission of waste. In this paper, the response of a number of these continuous monitors is compared with waste destruction efficiency measurements from a laboratory scale, liquid-spray incinerator operated on fuel oil doped with model waste compounds: benzene, chlorobenzene, acrylonitrile, and chloroform. Total hydrocarbon and CH4 measurements are found to vary with waste emission in a nearly linear manner; however, a substantial increase in CO emission occurs before a significant amount of waste is released. These results suggest that CO may serve as an indicator of the approach of waste release, while total hydrocarbons may provide an indicator of immediate waste release. 相似文献
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Tami A. Montgomery Gary S. Samuelsen Lawrence J. Muzio 《Journal of the Air & Waste Management Association (1995)》2013,63(5):721-726
Nitrous oxide (N2O) levels in the atmosphere are increasing, potentially contributing to the greenhouse effect and depletion of stratospheric ozone. From a limited data base, combustion sources have been identified as a major anthropogenic source of N2O. However, the existing data base (obtained by traditional grab sampling techniques followed by gas chromatographic analysis) is in question due to the discovery of a sampling artifact. A continuous on-line N2O analyzer would enable and facilitate the accurate characterization of combustion sources over a range of operating conditions, and also aid in the development of an appropriate sampling technique. This paper addresses the development of a continuous measurement technique, and the evaluation and initial use of a field prototype continuous N2O analyzer developed at the UCI Combustion Laboratory in cooperation with a major instrument manufacturer. The analyzer is capable of measuring N2O levels down to a few ppm. The analyzer has been evaluated and used to study the N2O emissions from a pulverized coal-fired boiler. The N2O levels found with the analyzer are substantially lower than levels previously attributed to such sources. Initial N2O measurements made with the analyzer suggest that N2O levels are not a substantial fraction of the NOX levels, as previously suggested. 相似文献
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G.S. Samuelsen John N. Harman III 《Journal of the Air & Waste Management Association (1995)》2013,63(7):648-655
The present study reviews the sampling environments and chemical transformations of nitrogen oxides that may occur within probes and sample lines while sampling combustion products. Experimental data are presented for NOx transformations in silica and 316 stainless steel tubing when sampling simulated combustion products in the presence of oxygen, carbon monoxide, and hydrogen. A temperature range of 25° to 400°C is explored. In the absence of CO and H2, 316 stainless steel is observed to promote the reduction of nitrogen dioxide to nitric oxide at temperatures in excess of 300°C, and silica is found to be passive to chemical transformation. In the presence of CO, reduction of N02 to NO is observed in 316 stainless steel at temperatures in excess of 100°C, and reduction of NO2 to NO in silica is observed at 400°C. In the presence of H2, NO2 is reduced to NO in 316 stainless steel at 200°C and NOx is removed at temperatures exceeding 200°C. In silica, the presence of H2 promotes the reduction of NO2 to NO at 300°C and the removal of NOx above 300°C. 相似文献
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