Download or read book Adsorption and Desorption of Mercury from Sorbents in a Hot Air Stream written by Amit Ghai and published by . This book was released on 1996 with total page 208 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Modeling of Adsorption and Desorption of Mercury on Sorbents in a Fixed Bed Absorber written by Feng Guo and published by . This book was released on 1997 with total page 180 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Mercury Adsorption and Desorption Kinetics written by Mark A. Bentley and published by . This book was released on 2012 with total page 132 pages. Available in PDF, EPUB and Kindle. Book excerpt: Mercury emissions in the United States are regulated under the Clean Air Mercury Rule. Multiple mercury removal technologies have been investigated and at this time, activated carbon injection into flue gas has been considered to be an efficient and economically feasible method for the removal of elemental mercury. Also, chemical modifications to activated carbon have shown to increase its mercury sorption capacity and removal efficiency. In this study, adsorption of elemental mercury onto ferric chloride impregnated activated carbon was investigated. The results show that ferric chloride impregnated activated carbon has a higher mercury sorption capacity than raw activated carbon does. A chemisorption mechanism was proposed and confirmed based on the characterization tests of fresh and spent sorbents. A kinetic study for the regeneration of spent sorbents was also conducted. The activation energies of mercury desorption from various substrates were calculated and the corresponding mercury desorption profiles were mathematically modeled.
Download or read book Development and Evaluation of Nanoscale Sorbents for Mercury Capture from Warm Fuel Gas written by Raja A. Jadhav and published by . This book was released on 2006 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Several different types of nanocrystalline metal oxide sorbents were synthesized and evaluated for capture of mercury (Hg) from coal-gasifier warm fuel gas. Detailed experimental studies were carried out to understand the fundamental mechanism of interaction between mercury and nanocrystalline sorbents over a range of fuel gas conditions. The metal oxide sorbents evaluated in this work included those prepared by GTI's subcontractor NanoScale Materials, Inc. (NanoScale) as well as those prepared in-house. These sorbents were evaluated for mercury capture in GTI's Mercury Sorbent Testing System. Initial experiments were focused on sorbent evaluation for mercury capture in N{sub 2} stream over the temperature range 423-533 K. These exploratory studies demonstrated that NanoActive Cr{sub 2}O{sub 3} along with its supported form was the most active of the sorbent evaluated. The capture of Hg decreased with temperature, which suggested that physical adsorption was the dominant mechanism of Hg capture. Desorption studies on spent sorbents indicated that a major portion of Hg was attached to the sorbent by strong bonds, which suggested that Hg was oxidized by the O atoms of the metal oxides, thus forming a strong Hg-O bond with the oxide. Initial screening studies also indicated that sulfided form of CuO/alumina was the most active for Hg capture, therefore was selected for detailed evaluation in simulated fuel gas (SFG). It was found that such supported CuO sorbents had high Hg-sorption capacity in the presence of H{sub 2}, provided the gas also contained H{sub 2}S. Exposure of supported CuO sorbent to H{sub 2}S results in the formation of CuS, which is an active sorbent for Hg capture. Sulfur atom in CuS forms a bond with Hg that results into its capture. Although thermodynamically CuS is predicted to form unreactive Cu{sub 2}S form when exposed to H{sub 2}, it is hypothesized that Cu atoms in such supported sorbents are in ''dispersed'' form, with two Cu atoms separated by a distance longer than required to form a Cu{sub 2}S molecule. Thus CuS remains in the stable reactive form as long as H{sub 2}S is present in the gas phase. It was also found that the captured Hg on such supported sorbents could be easily released when the spent sorbent is exposed to a H2-containing stream that is free of Hg and H{sub 2}S. Based on this mechanism, a novel regenerative process has been proposed to remove Hg from fuel gas at high temperature. Limited multicyclic studies carried out on the supported Cu sorbents showed their potential to capture Hg from SFG in a regenerative manner. This study has demonstrated that supported nanocrystalline Cu-based sorbents have potential to capture mercury from coal syngas over multiple absorption/regeneration cycles. Further studies are recommended to evaluate their potential to remove arsenic and selenium from coal fuel gas.
Download or read book Kinetic Modeling of Mercury Desorption and Adsorption on Fixed bed Sorbents written by Youngkil Lee and published by . This book was released on 1999 with total page 240 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Fundamental Understanding of Mercury Removal from Coal Combustion written by Erdem Sasmaz and published by Stanford University. This book was released on 2011 with total page 195 pages. Available in PDF, EPUB and Kindle. Book excerpt: Coal-fired power plants are a major anthropogenic source of worldwide mercury (Hg) emissions. Since mercury is considered to be one of the most toxic metals found in the environment, Hg emissions from coal-fired power plants is of major environmental concern. Mercury in coal is vaporized into its gaseous elemental form throughout the coal combustion process. Elemental Hg can be oxidized in subsequent reactions with other gaseous components (homogeneous) and solid materials (heterogeneous) in coal-fired flue gases. While oxidized Hg in coal-fired flue gases is readily controlled by its adsorption onto fly ash and/or its dissolution into existing solution-based sulfur dioxide (SO2) scrubbers, elemental Hg is not controlled. The extent of elemental Hg formed during coal combustion is difficult to predict since it is dependent on the type of coal burned, combustion conditions, and existing control technologies installed. Therefore, it is important to understand heterogeneous Hg reaction mechanisms to predict the speciation of Hg emissions from coal-fired power plants to design and effectively determine the best applicable control technologies. In this work, theoretical and experimental investigations have been performed to investigate the adsorption and in some cases the oxidation, of Hg on solid surfaces, e.g., calcium oxide (CaO), noble metals and activated carbon (AC). The objective of this research is to identify potential materials that can be used as multi-pollutant sorbents in power plants by carrying out both high-level density functional theory (DFT) electronic structure calculations and experiments to understand heterogeneous chemical pathways of Hg. This research uses a fundamental science-based approach to understand the environmental problems caused by coal-fired energy production and provides solutions to the power generation industry for emissions reductions. Understanding the mechanism associated with Hg and SO2 adsorption on CaO will help to optimize the conditions or material to limit Hg emissions from the flue gas desulfurization process. Plane-wave DFT calculations were used to investigate the binding mechanism of Hg species and SO2 on the CaO(100) surface. The binding strengths on the high-symmetry CaO adsorption sites have been investigated for elemental Hg, SO2, mercury chlorides (HgCl and HgCl2) and mercuric oxide (HgO). It has been discovered that HgCl, HgCl2, and SO2 chemisorb on the CaO(100) surface at 0.125 ML coverage. Binding energies of elemental Hg are minimal indicating a physisorption mechanism. Noble metals such as palladium (Pd), gold (Au), silver (Ag), and copper (Cu) have been proposed to capture elemental Hg. Plane-wave DFT calculations have been carried out to investigate the mercury interactions with Pd binary alloys and overlays in addition to pure Pd, Au, Ag, and Cu surfaces. It has been determined that Pd has the highest mercury binding energy in comparison to other noble metals. In addition, Pd is found to be the primary surface atom responsible for increasing the adsorption of Hg with the surface in both Pd binary alloys and overlays. Deposition of Pd overlays on Au and Ag has been found to enhance the reactivity of the surface by shifting the d-states of surface atoms up in energy. The possible binding mechanisms of elemental Hg onto virgin, brominated and sulfonated AC fiber and brominated powder AC sorbents have been investigated through packed-bed experiments in a stream of air and simulated flue gas conditions, including SO2, hydrogen chloride (HCl), nitrogen oxide (NO) nitrogen dioxide (NO2). A combination of spectroscopy and plane-wave DFT calculations was used to characterize the sorption process. X-ray photoelectron spectroscopy (XPS) and x-ray absorption fine structure (XAFS) spectroscopy were used to analyze the surface and bulk chemical compositions of brominated AC sorbents reacted with Hg0. Through XPS surface characterization studies it was found that Hg adsorption is primarily associated with halogens on the surface. Elemental Hg is oxidized on AC surfaces and the oxidation state of adsorbed Hg is found to be Hg2+. Though plane-wave DFT and density of states (DOS) calculations indicate that Hg is more stable when it is bound to the edge carbon atom interacting with a single bromine bound atop of Hg, a model that includes an interaction between the Hg and an additional Br atom matches best with experimental data obtained from extended x-ray absorption fine structure (EXAFS) spectroscopy. The flue gas species such as HCl and bromine (Br2) enhance the Hg adsorption, while SO2 is found to decrease the Hg adsorption significantly by poisoning the active sites on the AC surface. The AC sorbents represent the most market-ready technology for Hg capture and therefore have been investigated by both theory and experiment in this work. Future work will include similar characterization and bench-scale experiments to test the metal-based materials for the sorbent and oxidation performance.
Download or read book Mercury Desorption from Sorbents at Elevated Temperatures written by Puze Yang and published by . This book was released on 1998 with total page 224 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Masters Theses in the Pure and Applied Sciences Accepted by Colleges and Universities of the United States and Canada written by and published by . This book was released on 1996 with total page 442 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Methods and Sorbents for Utilizing a Hot side Electrostatic Precipitator for Removal of Mercury from Combustion Gases written by and published by . This book was released on 2011 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Methods are provided for reducing emission of mercury from a gas stream by treating the gas with carbonaceous mercury sorbent particles to reduce the mercury content of the gas; collecting the carbonaceous mercury sorbent particles on collection plates of a hot-side ESP; periodically rapping the collection plates to release a substantial portion of the collected carbonaceous mercury sorbent particles into hoppers; and periodically emptying the hoppers, wherein such rapping and emptying are done at rates such that less than 70% of mercury adsorbed onto the mercury sorbent desorbs from the collected mercury sorbent into the gas stream.
Download or read book Development and Evaluation of Nanoscale Sorbents for Mercury Capture from Warm Fuel Gas written by and published by . This book was released on 2006 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Gas Technology Institute (GTI), in collaboration with Nanoscale Materials, Inc. (NanoScale), is developing and evaluating several nanocrystalline sorbents for capture of mercury from coal gasifier (such as IGCC) warm fuel gas. The focus of this study is on the understanding of fundamental mechanism of interaction between mercury and nanocrystalline sorbents over a range of fuel gas conditions. Detailed chemical and structural analysis of the sorbents will be carried out using an array of techniques, such as XPS, SEM, XRD, N2-adsorption, to understand the mechanism of interaction between the sorbent and mercury. The proposed nanoscale oxides have significantly higher reactivities as compared to their bulk counterparts, which is a result of high surface area, pore volume, and nanocrystalline structure. These metal oxides/sulfides will be evaluated for their mercury-sorption potential in an experimental setup equipped with state-of-the-art analyzers. Initial screening tests will be carried out in N2 atmosphere, and two selected sorbents will be evaluated in simulated fuel gas containing H2, H2S, Hg and other gases. The focus will be on development of sorbents suitable for higher temperature (420-640 K) applications. As part of this Task, several metal oxide (MeO)-based sorbents were evaluated for capture of mercury (Hg) in simulated fuel gas (SFG) atmosphere at temperatures in the range 423-533 K. Nanocrystalline sorbents prepared by NanoScale Materials, Inc. (NanoScale) as well as in-house (GTI) sorbents were evaluated. These supported sorbents were found to be effective in capturing Hg at 423 and 473 K. Based on the desorption studies, physical adsorption was found to be the dominant capture mechanism with lower temperatures favoring capture of Hg. A nanocrystalline sorbent formulation captured 100% of Hg at 423 K with a 4-hr Hg-sorption capacity of 2 mg/g (0.2 wt%) in SFG. The high capacity of the nanocrystalline sorbent is believed to be the result of its high surface area and small crystallite size.
Download or read book Kinetic Study of Mercury Sorption Desorption Process on Sorbents written by T. C. Ho and published by . This book was released on 1999 with total page 6 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Novel Process for Removal and Recovery of Vapor Phase Mercury written by and published by . This book was released on 1998 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: We demonstrated in the Phase I program all key attributes of a new technology for removing mercury from flue gases, namely, a) removal of greater than 95% of both elemental and oxidized forms of mercury, both in the laboratory and in the field b) regenerability of the sorbent c) ability to scale up, and d) favorable economics. The Phase I program consisted of four tasks other than project reporting: Task I-1 Screen Sorbent Configurations in the Laboratory Task I-2 Design and Fabricate Bench-Scale Equipment Task I-3 Test Bench-Scale Equipment on Pilot Combustor Task I-4 Evaluate Economics Based on Bench-Scale Results In Task I-1, we demonstrated that the sorbents are thermally durable and are regenerable through at least 55 cycles of mercury uptake and desorption. We also demonstrated two low-pressure- drop configurations of the sorbent, namely, a particulate form and a monolithic form. We showed that the particulate form of the sorbent would take up 100% of the mercury so long as the residence time in a bed of the sorbent exceeded 0.1 seconds. In principle, the particulate form of the sorbent could be imbedded in the back side of a higher temperature bag filter in a full-scale application. With typical bag face velocities of four feet per minute, the thickness of the particulate layer would need to be about 2000 microns to accomplish the uptake of the mercury. For heat transfer efficiency, however, we believed the monolithic form of the sorbent would be the more practical in a full scale application. Therefore, we purchased commercially-available metallic monoliths and applied the sorbent to the inside of the flow channels of the monoliths. At face velocities we tested (up to 1.5 ft/sec), these monoliths had less than 0.05 inches of water pressure drop. We tested the monolithic form of the sorbent through 21 cycles of mercury sorption and desorption in the laboratory and included a test of simultaneous uptake of both mercury and mercuric chloride. Overall, in Task I-1, we found that the particulate and monolith forms of the sorbent were thermally stable and durable and would repeatedly sorb and desorb 100% of the mercury, including mercuric chloride, with low pressure drop and short residence times at realistic flue gas conditions.
Download or read book Development and Evaluation of Nanoscale Sorbents for Mercury Capture from Warm Fuel Gas Evaluation of Binary Metal Oxides for Mercury Capture written by Howard Meyer and published by . This book was released on 2006 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Gas Technology Institute (GTI), in collaboration with Nanoscale Materials, Inc. (NanoScale), is developing and evaluating several nanocrystalline sorbents for capture of mercury from coal gasifier (such as IGCC) warm fuel gas. The focus of this study is on the understanding of fundamental mechanism of interaction between mercury and nanocrystalline sorbents over a range of fuel gas conditions. Detailed chemical and structural analysis of the sorbents will be carried out using an array of techniques, such as XPS, SEM, XRD, N{sub 2}-adsorption, to understand the mechanism of interaction between the sorbent and mercury. The proposed nanoscale oxides have significantly higher reactivities as compared to their bulk counterparts, which is a result of high surface area, pore volume, and nanocrystalline structure. These metal oxides/sulfides will be evaluated for their mercury-sorption potential in an experimental setup equipped with state-of-the-art analyzers. Initial screening tests will be carried out in N{sub 2} atmosphere, and two selected sorbents will be evaluated in simulated fuel gas containing H{sub 2}, H{sub 2}S, Hg and other gases. The focus will be on development of sorbents suitable for higher temperature (420-640 K) applications. In this Task, several formulations of binary metal oxide-based sorbents were prepared and evaluated for capture of mercury (Hg) in simulated fuel gas (SFG) atmosphere at temperatures in the range 423-533 K. The binary metal oxides with high surface area were found to be more effective, confirming the role of sorbent surface in mercury capture. These binary sorbents were found to be effective in capturing Hg at 473 and 533 K, with Hg capture decreasing at higher temperature. Based on the desorption studies, physical adsorption was found to be the dominant capture mechanism with lower temperatures favoring capture of Hg.
Download or read book COMBINED THEORETICAL AND EXPERIMENTAL INVESTIGATION OF MECHANISMS AND KINETICS OF VAPOR PHASE MERCURY UPTAKE BY CARBONACEOUS SURFACES written by and published by . This book was released on 2000 with total page 8 pages. Available in PDF, EPUB and Kindle. Book excerpt: The overall goal of this research program is to gain fundamental understanding of the important chemistry and physics involved in mercury adsorption on carbonaceous surfaces. This knowledge will then be used to optimize adsorption processes and operating conditions to maximize the uptake of mercury within the required contact time. An additional long-term benefit of this research is the basic understanding of the Hg adsorption process, which may facilitate the design of new adsorbents for more efficient and cost-effective removal of Hg from a variety of effluent streams. Molecular modeling of the adsorption of Hg on carbonaceous surfaces will greatly increase the insight into the physics of the adsorption process and combined with in situ rate measurements of mercury adsorption and desorption (conventional and pulsed laser) on graphite using linear and nonlinear optical probes with real time optical resolution have the potential to provide fundamental insight into the process of mercury uptake by carbonaceous surfaces. Besides accurate assessment of key parameters influencing adsorption equilibrium, fundamental understanding of the kinetics of mercury adsorption, desorption, and diffusion will be developed in this study. These key physical and chemical processes postulated through molecular modeling efforts and verified by in situ measurements will be utilized to select (or develop) promising sorbents for mercury control, which will be tested under dynamic conditions using simulated flue gas.
Download or read book L din Max 1919 written by and published by . This book was released on 1939 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Zeitungsausschnitte.
Download or read book Control Techniques for Mercury Emissions from Extraction and Chlor alkali Plants written by United States. Environmental Protection Agency. Office of Air and Water Programs and published by . This book was released on 1973 with total page 84 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Mercury Control with Calcium Based Sorbents and Oxidizing Agents written by Thomas K. Gale and published by . This book was released on 2005 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: This Final Report contains the test descriptions, results, analysis, correlations, theoretical descriptions, and model derivations produced from many different investigations performed on a project funded by the U.S. Department of Energy, to investigate calcium-based sorbents and injection of oxidizing agents for the removal of mercury. Among the technologies were (a) calcium-based sorbents in general, (b) oxidant-additive sorbents developed originally at the EPA, and (c) optimized calcium/carbon synergism for mercury-removal enhancement. In addition, (d) sodium-tetrasulfide injection was found to effectively capture both forms of mercury across baghouses and ESPs, and has since been demonstrated at a slipstream treating PRB coal. It has been shown that sodium-tetrasulfide had little impact on the foam index of PRB flyash, which may indicate that sodium-tetrasulfide injection could be used at power plants without affecting flyash sales. Another technology, (e) coal blending, was shown to be an effective means of increasing mercury removal, by optimizing the concentration of calcium and carbon in the flyash. In addition to the investigation and validation of multiple mercury-control technologies (a through e above), important fundamental mechanism governing mercury kinetics in flue gas were elucidated. For example, it was shown, for the range of chlorine and unburned-carbon (UBC) concentrations in coal-fired utilities, that chlorine has much less effect on mercury oxidation and removal than UBC in the flyash. Unburned carbon enhances mercury oxidation in the flue gas by reacting with HCl to form chlorinated-carbon sites, which then react with elemental mercury to form mercuric chloride, which subsequently desorbs back into the flue gas. Calcium was found to enhance mercury removal by stabilizing the oxidized mercury formed on carbon surfaces. Finally, a model was developed to describe these mercury adsorption, desorption, oxidation, and removal mechanisms, including the synergistic enhancement of mercury removal by calcium.
