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Träfflista för sökning "WFRF:(Boström Dan) ;pers:(Boman Christoffer);pers:(Backman Rainer)"

Search: WFRF:(Boström Dan) > Boman Christoffer > Backman Rainer

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  • Boström, Dan, et al. (author)
  • Ash transformation chemistry during combustion of biomass
  • 2012
  • In: Energy & Fuels. - Washington DC : American Chemical Society (ACS). - 0887-0624 .- 1520-5029. ; 26:1, s. 85-93
  • Journal article (peer-reviewed)abstract
    • There is relatively extensive knowledge available concerning ash transformation reactions during combustion of woody biomass. In recent decades, the use of these energy carriers has increased, from a low-technology residential small-scale level to an industrial scale. Along this evolution, ash chemical-related phenomena for woody biomass have been observed and studied. Therefore, presently the understanding for these are, if not complete, fairly good. However, because the demand for CO2-neutral energy resources has increased recently and will continue to increase in the foreseeable future, other biomasses, such as, for instance, agricultural crops, have become highly interesting. The ash-forming matter in agricultural biomass is rather different in comparison to woody biomass, with a higher content of phosphorus as a distinctive feature. The knowledge about the ash transformation behavior in these systems is far from complete. Here, an attempt to give a schematic but general description of the ash transformation reactions of biomass fuels is presented in terms of a conceptual model, with the intention to provide guidance in the understanding of ash matter behavior in the use of any biomass fuel, primarily from the knowledge of the concentrations of ash-forming elements. The model was organized in primary and secondary reactions. Restrictions on the theoretical model in terms of reactivity limitations and physical conditions of the conversion process were discussed and exemplified, and some principal differences between biomass ashes dominated by Si and P, separately, were outlined and discussed.
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5.
  • Boström, Dan, et al. (author)
  • Ash transformation chemistry during energy conversion of biomass
  • 2010
  • In: Proceedings of the International Conference on Impact of Fuel Quality on Power production and the Environment. - : Impacts of Fuel Quality.
  • Conference paper (other academic/artistic)abstract
    • There is relatively extensive knowledge available concerning ash transformation reactions during energy conversion of woody biomass. Traditionally, these assortments have constituted the main resources for heating in Sweden. In recent decades the utilization of these energy carriers has increased, from a low technology residential small scale level to industrial scale (e.g. CHP plants). Along this evolution ash-chemical related phenomena for woody biomass has been observed and studied. So, presently the understanding for these are, if not complete, fairly good. Briefly, from a chemical point of view the ash from woody biomass could be characterized as a silicate dominated systems with varying content of basic oxides and with relatively high degree of volatilization of alkali sulfates and chlorides. Thus, the main ash transformation mechanisms in these systems have been outlined. Here, an attempt to give a general description of the ash transformation reactions of biomass fuels is presented, with the intention to provide guidance in the understanding of ash matter behavior in the utilization of any biomass fuel, primarily from knowledge of the concentrations of ash forming elements but also by considering the physical condition in the specific combustion appliance and the physical characteristic of the biomass fuel. Furthermore, since the demand for CO2-neutral energy resources has increased the last years and will continue to do so in the foreseeable future, other biomasses as for instance agricultural crops has become highly interesting. Globally, the availability of these shows large variation. In Sweden, for instance, which is a relatively spare populated country with large forests, these bio-masses will play a secondary role, although not insignificant. In other parts of the world, more densely populated and with a large agricultural sector, such bio-masses may constitute the main energy bio-mass resource in the future. However, the content of ash forming matter in agricultural bio-mass is rather different in comparison to woody biomass. Firstly, the content is much higher; from being about 0.3 - 0.5% (wt) in stem wood, it can amount to between 2 and 10 %(wt) in agricultural biomass. In addition, the composition of the ash forming matter is different. Shortly, the main difference is due to a much higher content of phosphorus (occasionally also silicon) which has major consequences on the ash-transformation reactions. In many crops, the concentration of phosphorus and silicon is equivalent, which (depending on the concentration levels of basic oxides) may result in a phosphate dominated ash. The properties of this ash are in several aspects different from the silicate dominated woody biomass ash and will consequently behave differently in various types of energy conversion systems. The knowledge about phosphate dominated ash systems has so far been scarce. We have been working with these systems, both with basic and applied research, for about a decade know. Some general experiences and conclusions as well as some specific examples of our research will be presented
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6.
  • Boström, Dan, et al. (author)
  • Ash transformation chemisty during energy conversion of agricultural biomass
  • 2009
  • Conference paper (other academic/artistic)abstract
    • There is relatively extensive knowledge available concerning ash transformation reactions during energy conversion of woody biomass. Traditionally, these assortments have constituted the main resources for heating in Sweden. In recent decades the utilization of these energy carriers has increased, from a low technology residential small scale level to industrial scale (i.e. CHP plants). Along this evolution ash‐chemical related phenomena for woody biomass has been observed and studied. So, presently the understanding for these are, if not complete, fairly good. Briefly, from a chemical point of view the ash from woody biomass could be characterized as a silicate dominated systems with varying content of basic oxides and with relatively high degree of volatilization of alkali sulfates and chlorides. Thus, the main ash transformation mechanisms in these systems have been outlined. However, since the demand for CO2‐neutral energy resources has increased the last years and will continue to do so in the foreseeable future, other biomasses as for instance agricultural crops has become highly interesting. Globally, the availability of these shows large variation. In Sweden, for instance, which is a relatively spare populated country with large forests, these bio‐masses will play a secondary role, although not insignificant. In other parts of the world, more densely populated and with a large agricultural sector, such bio‐masses may constitute the main energy bio‐mass resource in the future. However, the content of ash forming matter in agricultural bio‐mass is rather different in comparison to woody biomass. Firstly, the content is much higher; from being about 0.3 – 0.5% (wt) in stem wood, it can amount to between 4 and 10 %(wt) in agricultural biomass. Furthermore, the composition of the ash forming matter is different . Shortly, the main difference is due to a much higher content of phosphorus which has major consequences on the ash‐transformation reactions. In many crops, the concentration of phosphorus and silicon is equivalent, which (depending on the concentration levels of basic oxides) may result in a phosphate dominated ash. The properties of this ash are in several aspects different from the silicate dominated woody biomass ash and will consequently behave differently in various types of energy conversion systems. The knowledge about phosphate dominated ash systems has so far been scarce. We have been working with these systems, both with basic and applied research, for about a decade know. Some general experiences and conclusions as well as some specific examples of our research will be presented.
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7.
  • Enestam, Sonja, et al. (author)
  • Occurrence of zinc and lead in aerosols and deposits in the fluidized bed combustion of recovered waste wood : Part 1: Samples from boilers
  • 2011
  • In: Energy & Fuels. - : American Chemical Society. - 0887-0624 .- 1520-5029. ; 25:4, s. 1396-1404
  • Journal article (peer-reviewed)abstract
    • Combustion of recovered waste wood (RWW) has led to increased fouling and corrosion of furnace walls, superheaters, and economizers. These problems have been associated mainly with chlorine, zinc, and lead in the deposits but also with sodium and titanium. The presence of lead and zinc compounds, especially lead and zinc chlorides, has been shown to increase the corrosivity of the deposits even at relatively low metal temperatures (230−450 °C). The present work determined experimentally the distribution and speciation of zinc and lead compounds in aerosol particles and deposits in the fluidized-bed combustion of RWW. Measurements were conducted in both a full-scale (20 MWth) plant with as-received RWW and in a pilot-scale (2 MWth) setup with as-received RWW and RWW doped with zinc and lead. The results show that the amount and speciation of zinc and lead in the deposits vary depending upon the fuel composition, flue gas temperature, and metal temperature. Both lead and zinc chlorides are found in temperature ranges typical for the primary superheater area. A caracolite-type compound [Na3Pb2(SO4)3Cl] was identified in deposits from the economizer area and K2ZnCl4 in the sub-micrometer aerosol particle fraction.
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10.
  • Öhman, Marcus, et al. (author)
  • Slag formation during combustion of biomass fuels
  • 2009
  • Conference paper (other academic/artistic)abstract
    • Slag and ash deposition problems have more than occasionally been observed in biomass fueled plants in general and especially in pellet fired plants. These problems could lead to reduced accessibility as well as performance of the combustion appliances. Slag formation including measures for prevention and prediction during combustion of biomass fuels has been studied by the research groups at Luleå University of Technology, Umeå University, Energy Technology Center and Swedish University of Agricultural Sciences for about one decade know. Several (about 40) different biomass fuels/fuel mixtures have been studies and many different fuel additives/co-combustion fuels have been used to combat slag formation. About 25 scientific papers and 10 technical reports have been published by the research groups within the topic of slag formation during combustion of biomass fuels. The general experiences and conclusions of our research within the area will be presented.
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