Biomass upgrading through torrefaction is expected to relevantly reduce biomass trade costs and thus energy costs for the end-user. In this framework, the present work aims at defining crucial technical and cost parameters for the production, fuel properties, supply and end-use of torrefied pellets. The findings are used to compare four real-case wood pellet with corresponding torrefied pellet supply chains. Input data are derived from laboratory fuel, pelletising and storage experiments with torrefied biomass provided from European producers, cost estimations based on experience from related technology engineering and set-up as well as from expert consultations. This allows a step-by-step comparison of cost advantages and additional expenses from pretreatment to end-user. As a result, torrefied pellets turn out to be a certain alternative for wood pellets. The cost comparison demonstrates that the production of torrefied pellets is still much more cost-intensive, but can be partly compensated by reduced transportation costs. At the end-user, heat production in small-scale pellet boilers is technically feasible, but with slightly higher costs. Co-firing torrefied pellets in large-scale coal plants can be cost-competitive to industrial wood pellets, when no additional retrofit and operation and maintenance costs incur.

Gegenstand der Arbeit ist der thermische und thermo-chemische Aufschluss von Biertrebern. Dabei werden die Prozessbedingungen wie Chemikalien, Konzentration, Aufschlusstemperatur sowie Aufschlussdauer und deren Einfluss auf die Biogasgewinnung untersucht. Der Nachweis erfolgt entlang den einzelnen Prozessstufen Hydrolyse, Acidogenese und Methanogenese. Die Prozessparameter der Aufschlüsse haben sowohl einen starken Einfluss auf die Hydrolyse der Lignozellulose als auch auf die Bildung thermischer Nebenprodukte. Diese Zwischenprodukte beeinflussen unter anderem den Schritt der Acidogenese stark. Wohingegen die Endprodukte, Melanoidine, anaerob kaum abbaubar sind und damit die Biogasausbeute reduzieren. Die höchsten Methanerträge werden mit einer Behandlungstemperatur von 140 °C erreicht. Unterschiedlich sind dabei die Höhe der zusätzlichen Gaserträge von 28 Vol.-% mit H2O sowie rund 50 Vol.-% mit Lauge und 60 Vol.-% mit Säure. In semi-kontinuierlich beschickten Reaktoren konnten mit unbehandelten Trebern Erträge von 410 m³N CH4/Mg oTS realisiert werden. Thermisch aufgeschlossene Treber ergeben Erträge von 468 m³N CH4/Mg oTS (+14 %). Durch die Zugabe von Lauge zum thermischen Aufschluss kann der Methanertrag auf 558 m³N/Mg oTS (+36 %) gesteigert werden. Auf Grund der Prozessinstabilitäten war der acido-thermisch aufgeschlossene Treber nicht auswertbar. Der Mehrertrag in den Aufschlüssen ist auf die verbesserte Verwertung der Zellulose und Hemizellulose zurückzuführen. Durch die Vorbehandlung der Biertreber gelingt es, die Treberverwertung wirtschaftlicher zu gestalten. Nach der Vergütung im Österreichischen Ökostromgesetz 2012 können Erträge von bis 13 €/Mg FM Treber erreicht werden. Dies ist insbesondere durch eine thermo-chemischen Vorbehandlung möglich

Wood pellets and wood raw materials such as chips or sawdust emit hazardous gases such as carbon monoxide (CO) and volatile organic compounds (VOCs) during processing and storage. Due to the high toxicity of CO it is necessary to identify the release mechanisms for CO and VOCs. Several studies show that organic extractives decrease during storage as well as the emissions. Therefore, the purpose of this study was to investigate a possible correlation between the organic extractive content and the release of CO and VOCs. Sawdust and pellets from Norway spruce (Picea abies), European larch (Larix decidua) and loblolly pine (Pinus taeda) were examined. Additionally, five different pellet samples from Austrian pellet producers were investigated. Soxhlet extraction with acetone was used to extract the organic content. The concentration of CO and VOCs was measured from stored wood materials and pellets in sealed glass flasks. The highest (3,41 mg CO/kg sample dm/d) and the lowest (0,02 mg CO/kg sample dm/d) release of CO were reported with freshly produced pine pellets and a spruce pellets sample from an Austrian do-it-yourself store, respectively. The results showed that the pelletizing process reduced the content of organic extractives. The emissions of pine samples concerning CO and VOCs were higher than of the spruce and larch samples. Moreover, the organic extractive content also decreased in that order. However, a direct correlation between organic extractive content and released quantities of emissions could not be established.

Der Schwerpunkt dieser Arbeit richtet sich auf die Kondensation von Aschedämpfen und die Feinstaubablagerung in Biomasse-befeuerten Kesseln. Zu diesem Zweck wurden in einer Versuchsanlage aschebildende Substanzen verdampft und anschließend auf einer gekühlten Sonde kondensiert. Als Modellsubstanz für die Aschedämpfe der Biomasse wurde Kaliumchlorid verwendet. Das Rauchgas wurde dabei mittels Verbrennung von Erdgas durch einen Gasbrenner zur Verfügung gestellt. Es sollten Informationen darüber gewonnen werden, welche Struktur die Depositionsschicht durch Kondensation oder Feinstaubablagerung ausbildet (Porosität, Homogenität, Festigkeit, Struktur) und wie die gebildete Depositionsschicht den Wärmeübergang beeinflusst. Die Berechnung des Kondensationsmassenstromes der aschebildenden Substanz mittels eines Ähnlichkeitsansatzes zum Wärmeübergang (Lewis-Ansatz) zeigt eine gute Übereinstimmung zu den experimentellen Versuchen. Die Depositionsschicht weist eine sehr hohe Porosität (p > 0,97) auf. Das Wärmeleitmodell „k maximum“ berechnet entsprechende Werte für die Wärmeleitfähigkeit der Depositionsschicht. Die Struktur der gebildeten Depositionsschicht ist von der Oberflächentemperatur der Sonde abhängig. Bei niedriger Sondentemperatur (T1 = 300 °C) bildet sich das Gefüge der Kondensationsschicht aus Kaliumchlorid als würfelförmige Kristalle aus, die „turmartig“ aufeinander herauswachsen. Diese Schicht zeichnet sich durch eine höhere Stabilität aus. Bei höherer Sondentemperatur (T2 = 500 °C) ist das Gefüge aus kleineren nadeligen und tröpfchenförmigen Kristallen aufgebaut, welche „baumartig“ herauswachsen. Wenn man die Kondensationsschicht am Depositionsring betrachtet wird ersichtlich, dass sich die Verteilung der Depositionsmenge in Abhängigkeit von der Depositionsmasse sehr unterschiedlich ausbildet. Bei geringer Depositionsmenge (m < 0,01 [g]) ist die Verteilung gleichmäßig um den Ring verteilt, bei höherer Depositionsmenge (m>0,01 [g]) befindet sich der Hauptteil der Depositionsmasse hauptsächlich auf der rauchgaszugewandten Seite der Sonde. Obwohl die Berechnung der Kondensationsmassenströme mit Hilfe des Ähnlichkeitsansatzes eine gute Übereinstimmung zeigt, sind die berechneten Werte stets etwas höher als die gemessenen Ergebnisse. Es wird vermutet, dass die Ursache in der hohen Instabilität der Depositionsschicht liegt, wodurch Erosionsvorgänge durch die vom Rauchgas erzeugten Schubspannungen die Depositionsschichtdicke reduzieren. Die Wärmeleitfähigkeit der Depositionsschicht ist aufgrund der hohen Porosität (hoher Anteil des fluiden Rauchgasanteils mit geringer Wärmeleitfähigkeit, kleiner Anteil des stark wärmeleitenden festen Kaliumchlorids) sehr niedrig, aber trotzdem deutlich höher als die Wärmeleitfähigkeit des Rauchgases. Sie liegt in der Größenordnung von k = 0,1-0,2 [W/mK]. Schon geringe Depositionsschichtmassen bewirken eine starke Verringerung des Wärmeüberganges und einen damit verbundenen hohen Temperaturgradienten in der Depositionsschicht. In dieser Arbeit wurden die für den Aufbau der Depositionsschicht maßgebenden Einflussfaktoren untersucht. Diese sind die Rauchgasgeschwindigkeit, die Salzfreisetzung, die Kondensationsdauer und die Oberflächentemperatur. Die Salzfreisetzung ist maßgebend für die Kondensationsmasse. Eine Verdoppelung der Salzfreisetzungsrate zeigte im untersuchten Wandbereich eine Verdoppelung der Kondensationsrate. Eine Verdoppelung der Rauchgasgeschwindigkeit führte zu einer geringen Abnahme der Kondensationsmasse bei gleichbleibenden Betriebsparametern, welches höchstwahrscheinlich durch Erosionsvorgänge bedingt ist. Die Sondenoberflächentemperatur zeigte im untersuchten Temperaturbereich von 300°C-500°C bei geringen Kondensationsmassen keinen Einfluss auf die Kondensationsrate. Bei größeren Depositionsschichten hatte die höhere Temperatur eine Verringerung der Kondensationsrate zur Folge.  

Fischer-Tropsch (FT) synthesis is one option to produce liquid transportation fuels from carbon-containing feedstocks. In the past, FT synthesis was used mainly to convert coal or natural gas to diesel and gasoline. In the last decade, much R&D effort has been made to use this technology to convert biomass to a high-quality transportation fuel. In this chapter, the technology for BtL (conversion of biomass to liquid transportation fuels over FT synthesis) is described, from synthesis gas production including requirements on the gas quality to a detailed description of the FT synthesis itself. The main focus of this chapter is to give an overview of the types of catalysts, also including their preparation, reduction, and aging; the types of FT reactors; and also the reaction conditions including kinetic laws and mechanistic proposals.

Heavy fractions resulting from mechanical treatment stages of mechanical-biological waste treatment plants are posing very specific demands with regard to further treatment (large portions of inert and high-caloric components). Based on the current Austrian legal situation such a waste stream cannot be landfilled and must be thermally treated. The aim of this research was to evaluate if an inert fraction generated from this waste stream with advanced separation technologies, two sensor-based [near-infrared spectroscopy (NIR), X-ray transmission (XRT)] and two mechanical systems (wet and dry) is able to be disposed of. The performance of the treatment options for separation was evaluated by characterizing the resulting product streams with respect to purity and yield. Complementing the technical evaluation of the processing options, an assessment of the economic and global warming effects of the change in waste stream routing was conducted. The separated inert fraction was evaluated with regard to landfilling. The remaining high-caloric product stream was evaluated with regard to thermal utilization. The results show that, in principal, the selected treatment technologies can be used to separate high-caloric from inert components. Limitations were identified with regard to the product qualities achieved, as well as to the economic expedience of the treatment options. One of the sensor-based sorting systems (X-ray) was able to produce the highest amount of disposeable heavy fraction (44.1%), while having the lowest content of organic (2.0% C_biogenic per kg waste input) components. None of the high-caloric product streams complied with the requirements for solid recovered fuels as defined in the Austrian Ordinance on Waste Incineration. The economic evaluation illustrates the highest specific treatment costs for the XRT (€23.15 per t), followed by the NIR-based sorting system (€15.67 per t), and the lowest costs for the air separation system (€10.79 per t). Within the ecological evaluation it can be shown that the results depend strongly on the higher heating value of the high caloric light fraction and on the content of Cbiogenic of the heavy fraction. Therefore, the XRT system had the best results for the overall GWP [-14 kg carbon dioxide equivalents (CO₂eq) per t of input waste] and the NIR-based the worst (193 kg CO₂ eq per t of input waste). It is concluded that three of the treatment options would be suitable under the specific conditions considered here. Of these, sensor-based sorting is preferable owing to its flexibility. © The Author(s) 2013.

An in-bed and an on-bed feeding system are implemented in a dual fluidized bed gasifier in order to investigate the influence of the fuel feeding position on the gasification process. Two bed materials, fresh and used olivine, are used because of their varying catalytic activity. The comparison of in-bed and on-bed feeding of wood pellets shows that in-bed feeding is more favorable, because lower tar concentrations are achieved and the gas composition is closer to water-gas shift equilibrium. Better mixing of bed material and fuel particles occurs with in-bed feeding. The residence time of the gas phase in the fluidized bed is longer in the case of in-bed feeding, and therefore better performance of the gasifier is achieved. Sufficient residence time of the fuel in the bubbling bed is important when a less active bed material is used. More active bed material is capable of compensating for the shorter residence time of the gas phase in contact with bed material during on-bed feeding. •Experimental investigation of in-bed and on-bed feeding.•Two bed materials (catalytic activity) and two fuels (devolatilization behavior).•In-bed feeding more favorable due to lower tar concentration and better gas quality.•Residence time of the gas phase in the fluidized bed is longer during in-bed feeding.•More active bed material compensates for shorter residence time of the gas phase. © 2013 Elsevier Ltd.

The influence of the distribution of fuel particle size on steam gasification was studied systematically in a dual fluidized bed gasifier. Pilot plant gasification experiments have been conducted using sawdust and pellets produced from the same raw material. Three different kinds of waste wood with a broad particle size distribution were also considered for comparison. The fuels differ in their content of particles smaller than 1 mm of equivalent diameter. With an increasing proportion of particles smaller than 1 mm, the product gas contained less H₂ and more CO and CH₄. Less product gas was generated and the concentration of tar increased. It is observed that entrainment of small fuel particles plays an important role in the dual fluidized bed gasifier. Based on the superficial gas velocity in the freeboard of the gasification reactor, a limiting diameter for the entrainment of fuel particles can be determined. Under the conditions investigated a total of 22 wt.% of fuel particles present in the mixture of sawdust and pellets was entrained very rapidly after feeding because of their size. They mainly devolatilize in the freeboard and only have limited contact with the catalytic bed material. Therefore, these volatiles are less likely to be reformed and more tar is found in the product gas. As a conclusion, the particle size determines the region where the thermal conversion of the fuel particle mainly takes place: within the fluidized bed or in the freeboard. © 2013 Elsevier B.V.
 

In order to gain deeper insights into aerosol formation processes during MSW combustion, test runs with a specially developed high-temperature aerosol measurement and sampling device, the so called high-temperature impactor (HTI), as well as subsequent chemical analyses of the particles sampled have been performed at a real-scale plant. The results show that aerosol formation during MSW combustion is based on the volatilisation of minor amounts of Si-, Ca-, Mg- and Al-compounds followed by nucleation in the fuel bed region which is then followed by excessive condensation of alkaline metal sulphates and especially chlorides in the radiative and the convective boiler sections. At lower flue gas temperatures in the superheater as well as the economiser section also the condensation of heavy metal (Zn, Pb) chlorides provides contributions to aerosol formation. © 2011 Elsevier B.V.

Access to affordable and renewable sources of energy is crucial to reducing poverty and enhancing rural development in countries of the global South. Straight vegetable oil was recently identified as a possible alternative to conventional biomass for rural energy supply. In this context, the Jatropha curcas Linn. species has been extensively investigated with regard to its potential as a biofuel feedstock. In contrast, only little is known about Jatropha mahafalensis Jum. & H. Perrier, which is an indigenous and endemic representative of the Jatropha genus in Madagascar. This paper explores the potential and suitability of J. mahafalensis as a biofuel feedstock. Seed samples were collected in the area of Soalara in south-western Madagascar in February and September 2011. Two agro-ecological zones (coastal area and calcareous plateau) and two plant age groups (below and above 10. years) were considered. These four sample groups were analyzed with regard to oil properties, element contents, and fatty acid profiles. Measured values differed greatly between the two harvests, probably owing to different climatic or storage conditions. No direct relation between age of trees or location and oil quality could be established. The analyses indicate that J. mahafalensis oil can be used in oil lamps, cooking stoves and stationary combustion engines for electrification or for biodiesel production. However, modifications in storage and extraction methods, as well as further processing steps are necessary to enable its utilization as a straight vegetable oil and feedstock for biodiesel production. If these technical requirements can be met, and if it turns out that J. mahafalensis oil is economically competitive in comparison with firewood, charcoal, paraffin and petroleum, it can be considered as a promising feedstock for rural energy supply. © 2013 International Energy Initiative.

Operating biomass stoves in modern buildings with tight shells often requires a room-independent air supply. One possibility to arrange this supply is to use a double-wall chimney with fresh air entering through the annular gap. For this setup, a mathematical model has been developed and checked with experimental data. It turned out that for commercially available chimneys, leakage is not negligible and inclusion of leak air in the calculation is crucial for reproduction of the experimental data. Even with inclusion of this effect, discrepancies remain which call for further investigations and a refinement of the model.

The present paper introduces a life cycle modeling approach for representing actual demand of energy or energy intensive products delivered within a system (electricity, heat, etc.) for optimization of the energy mix, according to some of the available life cycle impact assessments (LCIAs). Unlike classical LCA modeling approach, the real amount of several energy products leaving the system and the interactions due to the presence of multi-output processes are considered within the present approach. As a case study, future scenarios are obtained for the Belgian electricity mix production and the heat mix potentially substituted by CHP or biomass, switching between abandoning or not power from nuclear energy. The possibility of using natural gas, biomass for cogeneration, wind power and solar photovoltaic energy are considered within the availability ranges of these resources. Finally, results are presented from successive optimizations according to the sustainability potential defined in a previous paper. A pathway to a more sustainable Belgian energy system is obtained. Finally it is concluded that under the modeling conditions and without nuclear energy it is not possible to obtain a reduction of GHGs and despite diminishing of non-renewable resource consumption, a rising of toxicity is obtained. © 2013 Elsevier Ltd.

Product gas produced by biomass gasification contains small amounts of sulfur compounds (hydrogen sulfide) which can reduce catalyst activity during steam reforming process. Sulfur removal has a negative effect on process efficiency and steam reforming has to be run without cleaning the gas prior to the reactor. It is therefore of interest to investigate the effect of sulfur on the performance of steam reforming reactions. In this work a packed bed reactor filled with nickel based catalysts is mathematically modeled to simulate the steady state pseudo-heterogeneous equations representing heat and mass transfer in the reactor tube. Catalytic bed is subjected to hydrogen sulfide and an isotherm model for the sulfur coverage on the Ni surface is considered to exactly investigate sulfur poisoning effects on methane conversion, hydrogen yield, carbon dioxide and carbon monoxide concentration. It is shown that even when present in the hydrocarbon feedstock in small quantities, (ppm) levels, sulfur can have a significant effect in methane conversion and temperature distribution within the reactor. © 2013 Elsevier B.V.

La combustione di biomassa legnosa con piccoli apparecchi e caldaie è oggi vista con rinnovato interesse per il raggiungimento degli obiettivi comunitari di produzione di energia rinnovabile al 2020. L’aumento dell’utilizzo della biomassa combustibile è di stretto interesse del settore agroforestale, per via del notevole indotto economico che peraltro interessa tutto il territorio nazionale. Tuttavia, la combustione della biomassa è legata ad una serie di problematiche ambientali quali le emissioni in atmosfera di polveri sottili che influenzano direttamente la qualità dell’aria. Si ritiene, quindi, che l’auspicato aumento dell’utilizzo delle biomasse, soprattutto ai fini della produzione di calore (riscaldamento ambienti), sia legata al contenimento delle emissioni al camino. In questo contesto, è quindi importante la corretta misura delle polveri emesse dagli apparecchi di riscaldamento domestico alimentati a biomassa solida, tenendo conto anche della frazione condensabile, come richiesto dalla normativa. Il lavoro mette a confronto due tecniche di misura delle polveri, la tecnica di prelievo a caldo con raffreddamento dei fumi in impinger e la tecnica di diluizione con tunnel. Sono stati selezionati per il confronto due apparecchi di ridotta potenza (< 15 kWt) ed elevata efficienza: una caldaia a pellet ed una stufa a pellet. In condizioni di combustione completa le due tecniche restituiscono fattori di emissione simili. Nella stufa a pellet la misura a freddo è maggiore del 20 – 30 % rispetto alla misura a caldo. La ridotta presenza della frazione condensabile è stata confermata dall’analisi NPOC degli impinger. Sono state misurate le emissioni totali prodotte da un utilizzo reale del dispositivo, comprendendo anche le fasi transitorie di combustione (accensione, riscaldamento a regime e spegnimento), solitamente non considerate nelle misure standard di laboratorio. La fase di accensione produce fino a tre volte le polveri emesse in condizioni stazionarie. L’emissione totale si riduce all’aumentare del tempo di utilizzo del dispositivo, rientrando nell’intervallo delle emissioni delle condizioni stazionarie dopo circa 6 h. Gli IPA, emessi in quantità elevate, sono costituiti maggiormente da congeneri a peso molecolare medio – basso, associati a minore tossicità. Il TEQ è funzione della potenza e delle condizioni di
combustione del dispositivo.