Firewood stoves are widespread and popular for renewable heat supply in Europe. Several new technological measures have been developed recently that aim at improving the appliance performance in terms of emissions and efficiency. In order to support the trend towards “(nearly) zero-emissions technologies”, the objective of this study was to provide a profound overview of the most relevant technical primary and secondary measures for emission reduction and to analyze their functionality, the relevant framework conditions for their application and their costs. Since user behavior is essential for emission and efficiency performance, the state of knowledge about user behavior is summarized and the latest measures for its optimization are evaluated as non-technical primary measures. Primary and secondary measures were analyzed separately, but also potentially promising combinations of primary and secondary optimization were evaluated using SWOT analysis. The results showed that complementary application of primary and secondary measures will be necessary in order to achieve “(nearly) zero-emission technologies”. The paper is useful for manufacturers and provides them with guidance and recommendations for future developments. They can specifically select appropriate measures for their products and applications not only based on technical aspects, but also with a strong focus on user behavior and user comfort.

The present study aims to present a comprehensive characterization of the surface of ash-layered olivine bed particles from dual fluidized bed gasification. It is well known from operation experience at industrial gasification plants that the bed material is activated during operation concerning its positive influence on gasification reactions. This is due to the built up of ash layers on the bed material particles; however, the chemical mechanisms are not well understood yet. Olivine samples from long-term operation in an industrial-scale gasification plant were investigated in comparison to fresh unused olivine. Changes of the surface morphology due to Ca-enrichment showed a significant increase of their surface area. Furthermore, the Ca-enrichment on the ash layer surface was distinctively associated to CaO being present. The presence of CaO on the surface was proven by adsorption tests of carbon monoxide as model compound. The detailed characterization contributes to a deeper understanding of the surface properties of ash layers and forms the basis for further investigations into their influence on gasification reactions.

Overview on different approaches for supervisory control strategies,deciding on operating modes and set points for the controls of the different plants and componentsintegrated in solar thermal systems.

This paper presents one part of the results of a project dealing with straw pellets combustion in small
scale combustion systems. Whereas the other part of the work investigates gaseous and particulate emissions, this part focuses on the results of experiments to determine corrosion of refractory material. Three different types of straw
pellets are combusted in a prototype of a 15 kW residential heating boiler. The fuel samples are natural wheat straw,
wheat straw with alumina based additive and wheat straw with a mixture of calcium-/magnesium carbonate based
additive. Combustion experiments are performed under different operating conditions of the test boiler. Three
different types of refractory material are used as combustion chamber material. The refractory materials are different
mixtures of alumina, silica, zirconia and silicium-carbide. The degree of deterioration of these materials is
investigated for temperatures between 700 and 1300 deg C in the presence of slag formed during combustion of the
straw samples and the influence of the fuel additives on corrosion effects is analysed.

Because of an increasing interest in the utilization of new and in terms of combustion-related properties rather unknown biomass fuels in heat and power production, advanced fuel characterization tools are gaining rising interest. Currently, ongoing research and development (R&D) focuses on a better and more precise description of the combustion properties of specific biomass fuels by applying new/advanced analysis methods and modeling tools. These novel characterization methods cover combustion tests in specially designed lab reactors, special fuel indices for biomass fuels, and the dedicated application of high-temperature equilibrium calculations. In this paper, a strategy is presented how the information gained from different advanced fuel characterization methods can be combined to characterize a fuel regarding its combustion behavior in a novel way. By means of this strategy, relevant qualitative and quantitative information regarding the ash-melting behavior, aerosol, SO_x, HCl, and NO_x emissions to be expected, and high-temperature corrosion risks can be gained. In addition, the approach can also be used for the evaluation of additives and fuel blending as measures to improve specific combustion properties. The results show that a much better and clearer picture about the combustion properties of a specific biomass fuel can be provided than by conventional approaches (such as wet chemical analysis or other standardized methods). The results can be used for the preliminary design of plants as well as for evaluation of the applicability of a specific technology for a certain biomass fuel or fuel spectrum. Moreover, they can be applied in combination with computational fluid dynamics (CFD) simulations for the detailed design and evaluation of furnaces and boilers. © 2014 American Chemical Society.

Biogas substrates are typically moist, which can make them difficult to store because bacteria and mould can grow on them. Ensiling, which involves the production of acid by lactic acid bacteria, is often used to preserve crops cheaply. Biogas substrates are also often fibrous, which can make them difficult to mix and means that some of their energy is locked up within the fibres. Different pre-treatment technologies are being investigated to access the energy in these fibres, to increase the rate of biogas production and to improve the mixing qualities of the substrates. Pre-treatment technologies are based on three principles: physical (including mechanical shear, heat, pressure and electric fields), chemical (acids, bases and solvents) and biological (microbial and enzymatic). Combinations of these principles are also used, including steam explosion, extrusion and thermo-chemical processes. Although many of these processes have been investigated at small scale, few have been analysed at large scale in un-biased studies. Many of these techniques are associated with high energy input (e.g. mechanical and heat pre-treatment), high equipment costs (e.g. mechanical systems where the blades erode) or use large volumes of chemicals (e.g. alkali pre-treatment). Different pre-treatment technologies work better with different substrates, and more research is required in this field to understand which combinations are worthwhile. This chapter describes some of the common pre-treatment technologies along with some advantages and disadvantages.

In order to enlarge the range of feedstock for the dual fluidized bed (DFB) gasification process, the influence of several fuel properties was studied in the 100 kW DFB pilot plant. Fuels with high concentration of nitrogen and sulfur, fuels with an increased concentration of fine particles, and fuels with extremely high content of volatiles were tested. The DFB gasification system is found to be robust and can handle all the materials. Nitrogen, sulfur and chlorine from the fuel are predominantly converted in the gasification reactor, either to gases (nitrogen, sulfur) or bound to ash (chlorine, sulfur). For the performance of the DFB gasifier, sufficient contact of fuel, product gas and bed material is important. Increasing amounts of fine particles or volatiles in the fuels lead to higher tar loads in the product gas, because the residence time of fuel particles in bubbling fluidized bed is shorter.

Steam gasification enables the thermochemical conversion of solid fuels into a medium calorific gas that can be utilized for the synthesis of advanced biofuels, chemicals or for heat and power production. Dual fluidized bed (DFB) gasification is at present the technology applied to realize gasification of biomass in steam environment at large scale. Few large-scale DFB gasifiers exist, and this work presents a compilation and analysis of the data and operational strategies from the six DFB gasifiers in Europe. It is shown that the technology is robust, as similar gas quality can be achieved despite the differences in reactor design and operation strategies. Reference concentrations of both gas components and tar components are provided, and correlations in the data are investigated. In all plants, adjusting the availability and accessibility to the active ash components (K and Ca) was the key to control the gas quality. The gas quality, and in particular the tar content of the gas, can conveniently be assessed by monitored the concentration of CH₄ in the produced gas. The data and experience acquired from these plants provide important knowledge for the future development of the steam gasification of biomass.

The objectives of the present study were to: (a) develop an appropriate estimation method for assessing the characteristic ash melting temperatures of different biomass fuels by means of thermodynamic equilibrium calculations (TEC) based on ash analysis data, (b) estimate the correlation between the results obtained from TEC and the experimentally received data for the melting temperatures using a TGA/DSC-method (thermogravimetric analysis/differential scanning calorimetry) and, (c) evaluate the applicability of the TEC and DSC methods as prediction tools for the melting behaviour of biomass ashes in relation to the conventional ash melting test according to DIN 51730. The results are presented for four selected biomass ash samples: straw, miscanthus, beech and bark (spruce). The agreement between the results obtained from TEC and experimental results (TGA/DSC and standard ash melting test) was reasonably good. For comparison between the experimental results and TEC regarding the deformation temperature it is recommended to utilize the temperature range between T15 and T30 estimated by TEC at 15 wt% and 30 wt% molten phase respectively. Differences between calculated melting temperatures T30 for straw (770°C) and bark (1,280°C) on the one side, and experimentally determined data on the other side are lower than 100°C. In the case of miscanthus and beech ash the prediction was with a deviation of around 200°C less precise. Flow temperatures measured as per standard test (DIN 51730) show generally a good agreement with the TEC fusion temperatures at 70 wt% of molten fraction (T70) for straw, miscanthus and bark ash. In case of beech ash is the TEC prediction of T70 (>1,600°C) moved to higher temperatures compared to experimental expected 1,380°C. The results of this study in combination with reliable databases and an appropriate calculation model, qualify the thermodynamic equilibrium calculations as a useful technique for a prediction of the ash melting behaviour including the assessment of characteristic melting temperatures.

Thermal treatment of residues and waste is an important issue with increasing demand. In this work two pathways of thermal waste treatment, incineration and gasification, are compared. For this purpose literature on both technologies has been reviewed and the state-of-art technology for waste incineration and gasification is presented. The comparison highlights the strengths and weaknesses of both technologies and identifies future potentials.

More and more waste is generated every year, which has to be disposed. There is a legal obligation to treat waste before it can be landfilled in the European Union. Thus, thermal waste treatment is a very important issue.
In this work two pathways of thermal waste treatment, incineration and gasification, are compared. For this purpose, literature on both technologies has been reviewed and the stateof‐art technology for waste incineration and gasification is presented. The comparison highlights the strengths and weaknesses of both technologies and identifies future potentials. In Europe waste incineration is the state‐of‐the‐art technology ensuring destruction of the pollutants and allowing recovery of the energy content of the waste. A waste incineration plant consists of a furnace, where the waste is incinerated and the chemically bonded energy of the waste is discharged as heat. The hot flue gases pass the heat to the water in the heating surfaces of the steam generator. The energy of the waste can be used for the generation of hot water, steam of electrical power. Then the flue gas has to be cleaned in the air pollution control system. Dust is precipitated, HCl and HF is removed in an acid scrubber and SO2 in an alkaline scrubber. A catalytic reaction destroys dioxins and furans and reduces the emissions of NOx. Due to waste incineration the volume of the residues, which have to be landfilled, is
reduced by 90%. The second pathway of thermal waste treatment is waste gasification, where solid carbonaceous materials are converted into combustible gases by reaction with gasification agents. Due to gas production, not only the energy content of the waste can be recovered but the product range is extended. The producer gas can be converted into heat and power in a conventional steam boiler but also combusted in gas engines or turbines with higher efficiencies. In a combined cycle plant the hot exhaust gas of the turbine can be used in a heat recovery steam generator to increase the efficiency even more. After further cleaning the producer gas is also a suitable feedstock for synthesis of liquid fuels, synthetic natural gas and other chemicals.
Waste gasification processes have been developed in the past, but the plants have been shut down because of economic reasons and/or technical problems. However, important research has been done in the field of biomass gasification and thus gasification technology has been improved markedly. The fluidised bed gasifier in Güssing is one of the most successful examples; this technology is about to be commercialised. Considering these developments, there is definitely interesting potential for waste gasification now and the design of a new waste gasification process based on the findings in biomass gasification will be the scope of future research work.

Solid oxide fuel cell (SOFC) models used in the past for biomass-to-power plant simulations are limited in their predictability of the carbon deposition risk. In this work, industrial-relevant cell designs were modeled in 2D-CFD considering detailed reaction kinetics which allowed more accurate performance simulations and carbon deposition risk assessments. Via a parametric study, the influence of varying cell operating conditions on the cell performance and carbon deposition risk was quantified when utilizing product gases from steam- and air gasification with varying steam addition. Considering the results from this parameter study and carbon deposition risk assessment, recommendations for promising gasifier-SOFC configurations and cell operating points for stable long-term operation are presented. For smaller-scale biomass-to-power systems, the utilization of product gas from air gasification in anode supported cells with Ni/zirconia-based anode can be recommended, with only moderate steam dilution of the product gas at 750°C cell operating temperature. For larger scales, steam gasification might be meaningful, offering a generally higher electrical efficiency and power output in fuel cells than air gasification. However, a higher risk for carbon deposition could be determined in comparison to air gasification. Hence, a cell temperature of 850°C besides the use of cells with Ni/ceria-based anodes is recommended.

The flue gas mass flow is one of the fundamental quantities of the combustion process in biomass boilers. Since it directly relates to the enthalpy flow entering the heat exchanger, its knowledge is highly advantageous for a sophisticated load control of the biomass boiler. It also includes information regarding the primary and secondary air mass flows as well as the mass flows of potentially occurring leakage air and thermally decomposed fuel. However, in practical application it is not possible to obtain a reliable measurement of the flue gas mass flow. For this reason, this work presents a soft-sensor for the on-line estimation of the flue gas mass flow in biomass boilers. The approach is robust against fouling of the relevant boiler components and is based on standard measurements which are typically available in biomass boilers. In addition, the soft-sensor offers the possibility of monitoring the degree of heat exchanger fouling.

To ensure that energy is optimally used on site in local energy grids/microgrids and to achieve cost and/or emission reduction targets, the technologies are controlled by predictive and adaptive microgrid controllers. Based on realtime measurement data as well as load, generation, market and weather forecasts, the optimal deployment plan for the local energy grid is thus calculated using mathematical
optimization algorithms. Synergies of different technologies and sectors (electricity, heating, cooling, mobility, etc.) are taken into account, resulting in high energy efficiency in the system.

District heating (DH) networks have the potential for intelligent integration and combination of renewable energy sources, waste heat, thermal energy storage, heat consumers, and coupling with
other sectors. For growing networks in close geographical proximity, often the possibility arises to couple them using bidirectional heat exchangers, possibly unlocking synergies and reducing costs for the consumers. Each DH network may consist of producers, consumers and thermal energy storage (TES) devices. Often, each of the coupled DH networks will be already controlled via low-level controllers. Hence, a high-level control approach is needed, that coordinates the heat exchange between the
networks and takes renewable energy sources and the TES capacities in each network into account. These supervisory controllers are generally referred to as energy management systems (EMS).

Recycling of phosphorus in combination with increased utilization of bioenergy can mitigate material and global warming challenges. In addition, co-combustion of different fuels can alleviate ash-related problems in thermal conversion of biomass. The aim of this study is to investigate the ash transformation reactions of mainly P in co-combustion of P-rich sewage sludge (SS) with K-rich sunflower husks (SH) and K- and Si-rich wheat straw (WS). Single pellets of 4 mixtures (10 and 30 wt % SS in WS and 15 and 40 wt % SS in SH) and pure SS were combusted in an electrically heated furnace at process temperatures relevant for fluidized bed combustion (800 and 950 °C). Collected ash fractions were analyzed by inductively coupled plasma techniques, ion chromatography, scanning electron microscopy–energy-dispersive X-ray spectroscopy, and X-ray diffraction. Thermodynamic equilibrium calculations were performed to interpret the results. Over 90% of K and P was found to be captured within the residual ash with 30–70% P in crystalline K-bearing phosphates for mixtures with low amounts of SS (WSS10 and SHS15). The significant share of K and P in the amorphous material could be important for P recovery. For the lower percentage mixtures of SS (WSS10 and SHS15), P in crystalline phases was mainly found in K-whitlockite and CaKPO4. For the higher percentage SS mixtures, most of P was found in whitlockites associated with Fe and Mg, and no crystalline phosphates containing K were detected. For P recovery, co-combustion of the lower SS mixtures is favorable, and they are suggested to be further studied concerning the suitability for plant growth.

Natural draft wood log stoves for residential bioheat production are very popular due to the low fuel costs, the ecological aspect of a renewable energy source and the visual appeal of the flame. However, they have rather high pollutant emissions, specially of unburnt products. The description of large wood logs conversion in stoves needs to be improved to allow a process optimization which can reduce these emissions. The transient conversion of a single wood log in a stove is experimentally investigated with test runs quenching the log after defined time intervals and measuring the flue gas composition and temperatures in the log and stove. The experiments have been described with a volumetric single particle model, which predicts with good accuracy the log conversion until a time of around 30 min, when pyrolysis is almost ending. At that point, log fragmentation takes place and smaller fragments are detached from the log falling onto the bed of embers. Despite the increase in external surface area, char oxidation takes place at a moderate rate. This last stage of wood log conversion in a stove is the most challenging to model. Finally, preliminary recommendations are provided for reducing CO emissions in wood log stoves.

A key factor for the further distribution of biomass boilers in modern energy systems is the capability of changing the applied feedstock during normal plant operation. This is only possible with the application of advanced control strategies that utilize knowledge about the state variables and varying fuel properties. However, neither the state variables nor the fuel properties are measurable during plant operation and, thus, need to be estimated. This contribution presents a method for the simultaneous real-time estimation of the state variables and the fuel properties in fixed-bed biomass boilers which is a novel approach in the field of biomass boilers. The method bases on an Extended Kalman Filter using a nonlinear dynamic model and measurement data from the combustion process. The estimated variables are the masses of dry fuel and water in the fuel bed as well as the fuel's bulk density, water content, chemical composition and lower heating value. The proposed method is easy to implement and requires moderate computational effort which increases the potential of its application at actual biomass boilers. The proposed method is verified with simulation studies and by test runs performed at a representative small-scale fixed-bed biomass boiler. The estimation results show a good agreement with the actual values, demonstrating that the proposed method is capable of accurately estimating the biomass boiler's state variables and simultaneously its fuel properties. For this reason, the presented method is a key technology to ensure the further distribution of biomass boilers in modern energy systems.

A key factor for the further distribution of biomass boilers in modern energy systems is the capability of changing the applied feedstock during normal plant operation. This is only possible with the application of advanced control strategies that utilize knowledge about the state variables and varying fuel properties. However, neither the state variables nor the fuel properties are measurable during plant operation and, thus, need to be estimated. This contribution presents a method for the simultaneous real-time estimation of the state variables and the fuel properties in fixed-bed biomass boilers which is a novel approach in the field of biomass boilers. The method bases on an Extended Kalman Filter using a nonlinear dynamic model and measurement data from the combustion process. The estimated variables are the masses of dry fuel and water in the fuel bed as well as the fuel’s bulk density, water content, chemical composition and lower heating value. The proposed method is easy to implement and requires moderate computational effort which increases the potential of its application at actual biomass boilers. The proposed method is verified with simulation studies and by test runs performed at a representative small-scale fixed-bed biomass boiler. The estimation results show a good agreement with the actual values, demonstrating that the proposed method is capable of accurately estimating the biomass boiler’s state variables and simultaneously its fuel properties. For this reason, the presented method is a key technology to ensure the further distribution of biomass boilers in modern energy systems.

To gain better insight into inorganic element release processes, test runs with a specially designed single particle reactor connected with an inductively coupled plasma mass spectrometer (ICP-MS) have been performed. Relevant combustion related parameters such as mass loss during thermal degradation, temperature development of the particle (surface and center), and composition of released gases were recorded. By coupling the reactor to an ICP-MS, time-resolved release profiles of relevant aerosol forming elements (S, Cl, K, Na, Zn, and Pb) were determined. Targeted and controlled interruptions of the experiments (quenching) after a certain time were performed to validate reactor performance and reliability of the measurements. Test runs with softwood and straw pellets (8 mm in diameter and about 20 mm in length) were performed at reactor temperatures of 700, 850, and 1000 °C under oxidizing conditions (5.6 or 4.2 vol % O₂). These test runs have revealed that the release ratios of volatile and semivolatile ash forming elements (S, Cl, K, Na, Zn, and Pb) generally increase as reactor temperatures rise. Moreover, regarding straw, higher Si and Al contents influence the release behavior of K, Na, Zn, and Pb. For K, existing release mechanisms proposed in the literature have been confirmed, and for Na it has been suggested that release mechanisms similar to K prevail. Especially during the starting phase of the experiment, a distinct temperature gradient exists from the surface to the center of the particle. Thus, different conversion phases occur in parallel in different layers of the particle, which has to be considered during the interpretation of the time-resolved release profiles of the main inorganic elements. Furthermore, transport limitations due to the occurrence of molten phases (especially for straw at reactor temperatures of 1000 °C) were obvious and could be directly derived from the online recorded release profiles. The targeted interruption of the ongoing decomposition process (quenching) provided an indication of the validity of the release profiles for S, K, Na, Zn, and Pb. Additionally, these experiments delivered valuable information regarding possible release mechanisms.

The interest in experimental data regarding thermal fuel decomposition as well as the release behavior of ash-forming elements of biomass fuels for modeling and simulation purposes is continuously increasing. On the basis of combustion experiments with lab-scale reactors and single-particle reactors, integral release data regarding ash-forming vapors can be obtained, whereby the release is calculated on the basis of analysis data of the fuel and the ash residues. At the moment, almost no time-resolved release data of ash-forming elements from single particles exist. Therefore, a single-particle reactor was designed, which has been coupled to an inductively coupled plasma mass spectrometer (ICP-MS). This reactor can be used for targeted experiments in a temperature range of 250–1050 °C under inert, reducing, and oxidizing conditions. With this reactor, it is possible to simultaneously determine the surface and center temperatures of a biomass particle, weight loss of the particle, and flue gas composition. The reactor has been coupled to an ICP-MS through a gas stream that is sufficiently diluted with Ar. First performance tests with pure salts (KCl, NaCl, (NH₄)₂SO₄, ZnCl₂, and PbCl₂) proved that relevant volatile ash-forming elements can be detected with the ICP-MS. For a further validation of the received signals, combustion tests with Miscanthus pellets have been carried out, whereby the controlled interruption of the experiments has also been investigated. These tests prove that with this system the simultaneous time-resolved determination of S, Cl, K, Na, Zn, and Pb is possible whereby the Cl signal can only be used with restrictions. On the basis of the determined release of ash-forming elements for the entire combustion experiment, a quantification/calibration of the measured intensities has been carried out. The data gained from these tests will provide deeper insights into release processes as well as form a relevant basis for release model development.

The processing of heterogeneous waste is a major challenge for waste treatment equipment used in mechanical-biological (MB) waste treatment plants. This conference contribution focuses on the technical feasibility and efficiency of different technologies for the processing of a heavy waste fraction from a MB-plant which contains a high portion of high caloric components. The aim is to meet the requirements for waste to be landfilled in Austria. Also economic considerations with regard to the implementation of an additional separation step and the resulting changes in the waste routing are discussed. The processing technologies looked at comprise sensor-based sorting technologies (NIR, X-ray transmission) as well as traditional mechanical density separation technologies such as a jigger and cross-flow air classification.

Biochar is attracting attention as an alternative carbon/fuel source to coal in the process industry and energy sector. However, it is prone to self-heating and often leads to spontaneous ignition and thermal runaway during storage, resulting in production loss and health risks. This study investigates biochar self-heating upon its contact with O2 at low temperatures, i.e., 50–300 °C. First, kinetic parameters of O2 adsorption and CO2 release were measured in a thermogravimetric analyzer using biochar produced from a pilot-scale pyrolysis process. Then, specific heat capacity and heat of reactions were measured in a differential scanning calorimeter. Finally, a one-dimensional transient model was developed to simulate self-heating in containers and gain insight into the influences of major parameters. The model showed a good agreement with experimental measurement in a closed metal container. It was observed that char temperature slowly increased from the initial temperature due to heat released during O2 adsorption. Thermal runaway, i.e., self-ignition, was observed in some cases even at the initial biochar temperature of ca. 200 °C. However, if O2 is not permeable through the container materials, the temperature starts decreasing after the consumption of O2 in the container. The simulation model was also applied to examine important factors related to self-heating. The results suggested that self-heating can be somewhat mitigated by decreasing the void fraction, reducing storage volume, and lowering the initial char temperature. This study demonstrated a robust way to estimate the cooling demands required in the biochar production process.

Steam gasification in a dual fluidized bed (DFB) reactor has already been developed in the power sector from lab- to commercial-scale for woody biomass as feedstock. A trend towards utilizing feedstock of lower quality, such as low-grade biomass, biogenic residues or waste drives the development of the technology in terms of reactor design, gas cleaning and optimizing operation parameters. Additionally, the need for production of sustainable end products more valuable than electricity and heat leads to the embedding of DFB gasification into complete process chains.

One promising technology in the field of residue valorization is the pyrolytic conversion of biomass to biochar. There are a lot of proven technologies for this task, with many of them being quite distinctive. Biochar has a lot of valuable properties and it shows potential to be applicated in many different fields of industry as a green carbon resource. Thus, as the demand for its production rises, more and more people from different fields share interest in the same technologies and the demand for guidance in form of readily available information increases. Two prominent technologies rather similar in appearance are rotary kilns and screw reactors. Both technologies consist of a long, hollow cylinder and both technologies use some form of longitudinal rotation as a means to transport feedstock. In this review, both technologies are described and their biggest differences and similarities are discussed, all under the aspect of biochar production. In total, 21 unique rotary kilns and 58 unique auger reactors were identified. The paper addresses process specific aspects, like heat supply or residence time, but it also gives an overview on current research and general aspects like scale-up considerations. Differences between both technologies were found in all of these aspects, with some of the most pronounced being the bigger maximum capacities and the greater residence time distributions in rotary kiln pyrolysis. Both technologies are viable candidates for producing biochar on a commercial level, however, literature comparing the influence of the reactor type on biochar properties was very scarce. As a future outlook it is recommended to produce data that can be compared on a quantitative level, so a more accurate assessment of each technologies up- and downsides can be made.

This work presents a methodology to perform the scale-up of a solid fuel furnace to a higher heat output with maintaining or improving the burn-out quality. As basis to derive the scale-up concept, an example of a 35 kW screw burner for biomass fuels is investigated. Based on the Pi-theorem, the relevant dimensionless parameters are derived and similarity rules for the scale-up are proposed as follows: As initial conditions, the height to diameter ratio of the combustion chamber, the mean Reynolds number in the combustion chamber and the mean square velocity through the combustion chamber shall be kept constant or in the case of the Reynolds number may also increase. Additionally the effective momentum flux ratio between the secondary air injected in the combustion chamber and the gases from the pyrolysis and gasification section also shall be kept constant to maintain the mixing conditions between combustible gases and secondary air. Finally the thermal surface load on the screw also shall be kept constant. The influence of different scale-up approaches on thermal surface load, gas velocity, pressure losses, Reynolds number and height-to-diameter ratio are compared and discussed and a scaling approach to increase the heat output from 35 kW to 150 kW is described. For a theoretical validation of the scale-up, CFD simulations are performed to investigate the predicted pollutant emissions and the pressure loss for the scaled 150 kW furnace.

A pyrolysis process can be used to split up the biomass in a volatile fraction poor in undesired substances (Cl, N, S,
Na and K) and a char fraction where these substances are concentrated. In this way cheap biomass can be used for cofiring in existing fossil fuel power stations without the danger of corrosion, deposition, and emission problems. The aim of the project is the development and demonstration of a biomass pretreatment process based on pyrolysis in the temperature range between 450-650 °C to split the energy in the biomass into volatiles with a low content of the above mentioned undesired compounds and char, where most of these pollutants are concentrated. The balance of the system can provide important results, such as the development of the product spectrum by a function of the operating parameters. Based on the results of the pilot plant a scale up to a capacity of 30 MWth fuel input and the connection with the coal fired power plant is currently investigated.

The idea of co-firing biomass in an already existing coal-fired power plant could play a major contribution in the reduction of carbon dioxide emissions. Huge amounts of unused biomass in terms of agricultural residues such as straw, which is a cheap and local feedstock, are often available. But due to the high amount of corrosive ash elements (K, Cl, etc.), the residues are usually not suitable for co-firing in a thermal power plant. Therefore, the feedstock is converted by low temperature pyrolysis into gaseous pyrolysis products and charcoal. A 3 MW pyrolysis pilot plant located next to a coal-fired power plant near Vienna was set up in 2008. For the process, an externally heated rotary kiln reactor with a design fuel power of 3 MW is used which can handle about 0.6-0.8 t/h straw. The aim is to investigate the fundamentals for scale-up to the desired size for co-firing in a coal-fired power plant. In addition to the desired fuel for the process, which is wheat straw, a testing series for DDGS was also performed. The high amount of pyrolysis oil in the gas had positive effects on the heating value of the pyrolysis gas. Chemical efficiencies of this pyrolysis pilot plant of up to 67% for pyrolysis temperatures between 450°C and 600°C can be reached. The focus of this work is set on the pyrolysis products and their behavior at different pyrolysis temperatures as well as the performance of the pyrolysis process. © 2012 Elsevier B.V.

A pyrolysis process can be used to split up the biomass in a volatile fraction poor in undesired substances (Cl, N, S,
Na and K) and a char fraction where these substances are concentrated. In this way cheap biomass can be used for cofiring in existing fossil fuel power stations without the danger of corrosion, deposition, and emission problems. The aim of the project is the development and demonstration of a biomass pretreatment process based on pyrolysis in the temperature range between 450-650 °C to split the energy in the biomass into volatiles with a low content of the above mentioned undesired compounds and char, where most of these pollutants are concentrated. The balance of the system can provide important results, such as the development of the product spectrum by a function of the operating parameters. Based on the results of the pilot plant a scale up to a capacity of 30 MWth fuel input and the connection with the coal fired power plant is currently investigated.

Recently, researchers have begun to study hybrid approaches to Microgrid techno-economic planning, where a reduced model optimizes the DER selection and sizing is combined with a full model that optimizes operation and dispatch. Though providing significant computation time savings, these hybrid models are susceptible to infeasibilities, when the size of the DER is insufficient to meet the energy balance in the full model during macrogrid outages. In this work, a novel hybrid optimization framework is introduced, specifically designed for resilience to macrogrid outages. The framework solves the same optimization problem twice, where the second solution using full data is informed by the first solution using representative data to size and select DER. This framework includes a novel constraint on the state of charge for storage devices, which allows the representation of multiple repeated days of grid outage, despite a single 24-h profile being optimized in the representative model. Multiple approaches to the hybrid optimization are compared in terms of their computation time, optimality, and robustness against infeasibilities. Through a case study on three real Microgrid designs, we show that allowing optimizing the DER sizing in both stages of the hybrid design, dubbed minimum investment optimization (MIO), provides the greatest degree of optimality, guarantees robustness, and provides significant time savings over the benchmark optimization.

A dried dairy processing sludge (sludge from wastewater treatment of an effluent from a milk processing plant) was pyrolysed in a single-particle reactor at different temperatures from 400 °C to 900 °C. NH₃ and HCN were measured online and offline by means of FTIR as well as by cumulative sampling in impinger bottles (in 0.05 M H₂SO₄ and 1 M NaOH, respectively) and analysed by photometric method. NO and NO₂ were measured online using a nitric oxide analyser while N₂O was measured by FTIR. Nitrogen (N) in the sludge and in the remaining char, char-N, was determined. Moreover, tar content in pyrolysis gas was measured and tar-N was determined. The results with respect to N mass balance closure are discussed. The different measurements techniques are compared. For pyrolysis at 520 ℃ and 700 ℃ nitrogen in the gas phase was mainly contained as N₂ (36 % and 40 % respectively), followed by NH₃ (15 % and 18 %), tar-N (10 % and 9 %), HCN (1 % and 3 %), NO (1 %) and NO₂ (0.2 %). The dairy processing sludge has very specific properties with organic-N present predominantly as proteins and a high content of inherent Ca. These characteristics affected the distribution of N. The amount of char-N was higher while the amount of tar-N lower than for sewage sludge from literature, at comparable pyrolysis temperature.

Most of the current pyrolysis/torrefaction mechanisms are not able to predict the composition of pyrolysis/torrefaction products. They usually lump the products as permanent gases, liquids (condensable species) and solid residuals. However, the composition of the emitted species is required to predict the calorific value of the torrgas and to model the possible subsequent gas phase reactions and the temperature distribution within the reactor. Therefore, in this work a mechanism from literature is applied for the first time to predict the composition of the torrgas as a combination of twenty typical species. Several experimental data sets from literature are used to evaluate the mechanism. Since the mechanism predicts several relevant species (>1% wt.) in the torrgas for which no experimental data in the literature are available, test runs at a lab-scale packed bed reactor have been performed to achieve more detailed data of torrgas composition for model validation. Among the species for which measured data are available, carbon monoxide and methanol are well predicted. The predictions of carbon dioxide, methane, formaldehyde, acetaldehyde and ethanol are qualitatively correct. The predictions of water vapour, acetic acid, propanal, ethylene and sugar components show deviations. However, yields of solid residual and total emitted gas and tar are well predicted by the mechanism.

In the last years sampling at various gasification plants has been performed at Bioenergy2020+. The equipment, which is based on the recommendations of the tar guideline, has been further developed and adjusted to specific needs. For an evaluation of the procedure different parts of the equipment were tested with a new developed gas-generating unit. Most effort has been performed at the absorption of BTXE-S and PAH in 2-propanol. Additionally new characterisation-methods for pyrolysis samples with SPE (Solid Phase Extraction) have been tested and a qualitative identification of main components could be achieved. Furthermore tests for stabilisation and storage of samples were done. The results of the investigations represent an ongoing optimisation-work with the aim of establishing an international working-group which will compile guidelines for sampling organic and inorganic components at gasification and pyrolysis plants with different new online and offline methods. The appendix delivers some useful data about the substances and dynamic precipitation in an investigated impinger step.

An established control strategy for biomass grate boilers based on a low-order nonlinear model is considered. Under ideal conditions, it achieves decoupled control of desired outputs by means of input–output linearization. The decoupling is gradually reduced and control performance deteriorates when actuator saturation occurs. This may be avoided by appropriately shaping the control strategy’s reference values. This contribution presents a method to do so by solving a sequence of linear programs. Its implementation requires the knowledge of typically unknown limits of mass-flows fed into the plant. An estimation strategy for these limits based on measurable quantities is thus proposed. Experimental data from three different scenarios is presented, in which the reference shaping improves tracking, mitigates wind-up phenomena and reduces emissions, respectively.

The incineration of waste wood is very often associated with ash-related problems (deposits, slagging and corrosion). This leads to short maintenance intervals, mainly needed to remove ash depositions, which result in significant power generation losses and high downtime costs. To avoid these problems, additives can be used, with particularly cost-effective additives being of great interest. On the one hand, the purpose of the additives is to reduce the Cl concentration in deposits on heat exchangers, which is the main cause for corrosion. On the other hand, the additives shall increase the ash melting temperature of deposits and hereby reduce deposit formation. In a first step the combustion behaviour of 3 different waste wood mixtures without and with the addition of various low-cost additives such as recycled gypsum, coal fly ash and iron sulphide with two different addition ratios were investigated in a laboratory reactor. Using the laboratory reactor allowed the determination of suitable additives and ratios of additivation for further investigations in the industrial plant. This approach represents a cost-effective and time-saving method for determining suitable additives and ratios of additivation. Based on the investigations carried out, the addition of 2% gypsum and 3% coal fly ash was recommended, since an improved ash melting behaviour can be expected with addition of gypsum and coal fly ash. These additives with the recommended mixing rates were then tested in a large scale CHP plant (a 40 MWth grate furnace with additional injection of wood dust above the grate). Extensive test runs were carried out without additive (as a reference), and with the additives focusing on dust formation (aerosols and total dust), deposit formation and the corrosion behaviour of superheaters. These investigations were accompanied by fuel and ash analyses (grate, cyclone and filter).

The incineration of waste wood is very often associated with ash-related problems (deposits, slagging and corrosion). This leads to short maintenance intervals, which result in significant power generation losses and high downtime costs. To avoid these problems, additives can be used, with particularly cost-effective additives being of great interest. Based on pre-evaluations, the addition of 2% gypsum and 3% coal fly ash was recommended, since an improved ash melting behaviour and reduced risk for high-temperature corrosion can be expected with addition of gypsum and coal fly ash. These additives with the recommended mixing rates were then investigated in a large-scale plant. Extensive investigations were carried out without additive (as a reference), and with the additives focusing on dust formation (aerosols and total dust), deposit formation and the corrosion behaviour of superheaters. These investigations were accompanied by fuel and ash analyses (grate, cyclone and filter). The addition of additives increased the amount of total dust in the flue gas up to 195% and 262% for gypsum and coal fly ash respectively. The chemical analysis of the total dust showed an enrichment of refectory species like Al for coal fly ash and Ca and Mg for gypsum which can positively influence the slagging behaviour. Aerosol measurements showed that the addition of coal fly ash minimised the amount of fine particulate matter, as less alkali metals (K and Na) were released into the gas phase. Gypsum addition increases the SO2 concentrations in the gas phase due to the decomposition of gypsum, as in the combustion chamber about 900°C are present. Due to the preferred sulphation reactions (binding of S to alkali metals) less Cl is bound to alkali metals and therefore the Cl concentrations in the aerosols were lower compared to the reference case. This effect was also found in the deposits sampled at the position of the superheater. Based on the chemical composition of deposits the molar 2S/Cl ratios were determined, which can be used to predict the risk for high temperature corrosion. The analysis data showed that an improvement concerning the high temperature corrosion risk is possible by adding coal fly ash, whereas a significant improvement in case of gypsum additions seems very likely. The measurements carried out so far showed the influence (built-up rate, chemical composition etc.) of the additive application on ash fractions, deposits and dusts. By taking a closer look at the change in chemical compositions of dusts and deposits, additives with an appropriate additivation ratio can be suggested. In case of coal fly ash 3% and in case of gypsum 1% additive related to dry fuel seems to be adequate additive ratios to positively influence the risk of high temperature corrosion and reduce the slagging behaviour.

Anaerobic digestion (AD) of sugar beet pressed pulp (SBPP) is a promising treatment concept. It produces biogas as a renewable energy source making sugar production more energy efficient and it turns SBPP from a residue into a valuable resource. In this study one- and two-stage mono fermentation at mesophilic conditions in a continuous stirred tank reactor were compared. Also the optimal incubation temperature for the pre-acidification stage was studied. The fastest pre-acidification, with a hydraulic retention time (HRT) of 4 days, occurred at a temperature of 55 °C. In the methanogenic reactor of the two-stage system stable fermentation at loading rate of 7 kg VS/m³ d was demonstrated. No artificial pH adjustment was necessary to maintain optimum levels in both the pre-acidification and the methanogenic reactor. The total HRT of the two-stage AD was 36 days which is considerably lower compared to the one-stage AD (50 days). The frequently observed problem of foaming at high loading rates was less severe in the two-stage reactor. Moreover the viscosity of digestate in the methanogenic stage of the two-stage fermentation was in average tenfold lower than in the one-stage fermentation. This decreases the energy input for the reactor stirring about 80 %. The observed advantages make the two-stage process economically attractive, despite higher investments for a two reactor system. © 2013 Springer Science+Business Media Dordrecht.
 

A workshop on sampling and analysis of gas impurities (mainly condensables (tar)) in gases from thermochemical conversion processes was held in Berlin at the 19th EU BC+E. Here the outcomes are shortly summarized and the activities in the after course of the workshop are briefly discussed. An international working group formed to further discuss the important topics of analytics in these gas families was formed. Further ongoing and planned activities will be mentioned.

Residential wood combustion is, besides particulate emissions, also linked to emissions of organic compounds, comprising various toxic substances such as polycyclic aromatic hydrocarbons (PAHs). Although, literature data has shown that highest emissions occur during maloperations caused by the user itself, most studies focus on lab-testing not reflecting the situation in the field. This study evaluates the real-life situation in Austria, investigating emissions of total suspended particles (TSP) and particle-bound substances of four manually operated room heaters commonly installed in people's homes. Measurements were conducted within a field measurement campaign realized in the scope of the Clean Air by biomass project. To evaluate the impact of the users' habit two types of combustion experiments were performed, one representing the diversity of possible maloperations and one realized under optimized conditions following a strict optimization protocol. As special focus was laid on PAHs, sampling was realized using a dilution system adapted for the use in the field. Generally, optimization lead to a clear decrease of most compounds (i.e. TSP, OC, EC, PAHs), however, emissions of the anhydrosugar levoglucosan were not affected at all. Total PAH emissions could be clearly reduced, moreover, optimization lead to a shift towards low molecular weight PAHs and thus, less toxic ones, clearly reflected by lower toxicity equivalents. Correlation analysis using the Spearman's rank method showed significantly high correlations among the individual PAH congeners, and rather low ones with other target substances.

Biomass combustion is a major contributor to ambient air pollution. Thus, knowing the real-life emissions of biomass heating systems is crucial. Within the project Clean Air by biomass a field measurement campaign was conducted. 15 biomass heating appliances were tested in households at the end user according to their usual operation. Emission factors for gaseous and particulate emissions, as well as for the genotoxic and carcinogenic substance benzo(a)pyrene, were evaluated and compared to current proposed European and Austrian emission factors used for emission inventories. Moreover, the shares of particles and benzo(a)pyrene in hot and cooled flue gas were determined. Results showed a high variability of emissions in the field. Highest values and ranges occurred for room heaters (TSPtotal: 226 mg/MJ). Biomass boilers showed clearly lower emission factors (TSPtotal: 184 mg/MJ) in the field than room heaters and also than the proposed European and Austrian emission factors, in many cases. Emission factors for tiled stoves showed a similar trend (TSPtotal: 67 mg/MJ). The share of condensable particles in the flue gas was remarkable. Especially benzo(a)pyrene was found mostly in the condensable fraction of the particles.

Biomass combustion is a major contributor to ambient air pollution. Thus, knowing the real-life emissions of biomass heating systems is crucial. Within the project Clean Air by biomass a field measurement campaign was conducted. 15 biomass heating appliances were tested in households at the end user according to their usual operation. Emission factors for gaseous and particulate emissions, as well as for the genotoxic and carcinogenic substance benzo(a)pyrene, were evaluated and compared to current proposed European and Austrian emission factors used for emission inventories. Moreover, the shares of particles and benzo(a)pyrene in hot and cooled flue gas were determined. Results showed a high variability of emissions in the field. Highest values and ranges occurred for room heaters (TSPtotal: 226 mg/MJ). Biomass boilers showed clearly lower emission factors (TSPtotal: 184 mg/MJ) in the field than room heaters and also than the proposed European and Austrian emission factors, in many cases. Emission factors for tiled stoves showed a similar trend (TSPtotal: 67 mg/MJ). The share of condensable particles in the flue gas was remarkable. Especially benzo(a)pyrene was found mostly in the condensable fraction of the particles.

Solid oxide fuel cells are a promising alternative to gas engines for combined heat and power production based on biomass gasification. The technical complexity of realizing gasifier – fuel cell couplings has limited the number of experiments conducted in the past. However, results from such experiments are of high importance for the evaluation of tar thresholds and operating conditions ensuring a stable operation of fuel cells. For the first time, it was possible to demonstrate for dozens of hours the operation of solid oxide fuel cells with real product gas from steam gasification with a steam-to-carbon ratio of 2 and a typical tar content for fluidized bed gasification. Four coupling experiments with industrial-relevant cell designs were conducted, demonstrating a stable operation for 30 h without structural degradation of the anodes for cells with nickel/ceria- and nickel/zirconia-based anodes at 800°C and 850°C, if heavy tars were partially removed (2.8–3.7 g·Nm−3 gravimetric tars). Raw gas operation (4.6–4.8 g·Nm−3 gravimetric tars) led to metal dusting effects on nickel contact meshes and nickel/zirconia-based anodes, whereas nickel/ceria-based anodes were less affected. Carbon deposited on the alumina support in all experiments whereby a change from pyrolytic to graphitic structure could be observed when increasing the temperature from 800°C to 850°C, thus significantly reducing the risk for blockages in the flow channels. Moreover, high tar and benzene conversion rates were observed. Concluding, operating temperatures of 850°C and the removal only of heavy tars can enable stable long-term operation with a tar-laden steam gasifier product gas, even without increasing the steam-to-carbon ratio to values exceeding two.

Biodiesel (rapeseed oil methyl ester) was aged in a Rancimat device at a temperature of 110°C and an air flow of 10 L/h. Time-resolved analyses applying gas chromatography-flame ionization detection, gas chromatography-mass spectrometry, and ion-exchange chromatography on the formation of aging products were performed. Formic and acetic acid, fatty acids with chain lengths from 5 to 18 carbon atoms, fatty acid methyl esters, and epoxides were quantified. After 12 h of aging, the concentrations of formic and acetic acid were 5600 ± 80 and 1360 ± 80 mg/kg, respectively. Fatty acid concentrations were in the range of <18-4200 mg/kg after 18 h of aging. Linoleic acid methyl ester and linolenic acid methyl ester (19 and 9.1 mass % of the non-aged fuel) were shown to be fully decomposed after 24 and 18 h of aging, respectively. After 51 h of aging, the concentration of oleic acid methyl ester (63 mass % of the non-aged fuel) decreased to 2.2 mass % and trans-epoxy stearic acid methyl ester and cis-epoxy stearic acid methyl ester reached concetrations of 5.9 and 0.7 mass %, respectively. The fuel composition shows only minor changes in early stages of aging, and a strong timely correlation of the formation of aging products with the end of the induction period of fuel was observed. © 2014 American Chemical Society.

In the presented work the fuel quality and basic data about production processes of wood pellets from
all over Europe are investigated. For this purpose pellets producers were interviewed and fuel samples were analysed. Information from 91 companies was evaluated, covering about 50% of the European pellets production capacity, and pellets samples of 51 companies from 18 different countries were examined. It was found, that the raw material for pellets production is mainly taken from local resources. 75% of the plants process soft wood, whereas the use of hard wood is more common in Eastern Europe, Italy, Spain and France. Regarding the fuel properties of the pellets, differences were mainly found with regard to ash content and mechanical durability. In spite of these strong variations, almost all samples fulfilled the requirements according to the respective quality standard declared, and a clear correlation of valid standards and available pellets qualities was observed.

Glycerol is a co-product compound of biodiesel production with an interesting heating value. In this work pyrolysis kinetic parameters for a pellet made with a mass fraction of 90% sawdust and a mass fraction of 10% glycerol are derived through thermogravimetric analysis. A new parallel reaction scheme with four components (cellulose, hemicellulose, lignin and glycerol) is adopted and the kinetic triplet for each component is derived using a model fitting approach applied to this particular kind of pellet. The isoconversional method Kissinger-Akahira-Sunose is employed both to provide initial values for model fitting simulations and to check final results. Results show that activation energies and pre-exponential factors are respectively: 149.7 kJ mol⁻¹ and 1.98*10¹¹ s⁻¹ for hemicellulose, 230.1 kJ mol⁻¹ and 1.84*10¹⁷ s⁻¹ for cellulose, 154.3 kJ mol⁻¹ and 5.14*10⁹ s⁻¹ for lignin, 74.5 kJ mol⁻¹ and 2.17*10⁵ s⁻¹ for glycerol with a first reaction order for all components, except for lignin (n = 2.6). Through evolved gas analysis it was demonstrated that the thermal degradation of glycerol contained in the pellet can increase hydrogen content in pyrolysis gases.

Current levels of ambient air fine particulate matter (PM_2.5) are associated with mortality and morbidity in urban populations worldwide. In residential areas wood combustion is one of the main sources of PM_2.5 emissions, especially during wintertime. However, the adverse health effects of particulate emissions from the modern heating appliances and fuels are poorly known. In this study, health related toxicological properties of PM₁ emissions from five modern and two old technology appliances were examined. The PM₁ samples were collected by using a Dekati® Gravimetric Impactor (DGI). The collected samples were weighed and extracted with methanol for chemical and toxicological analyses. Healthy C57BL/6J mice were intratracheally exposed to a single dose of 1, 3, 10 or 15mg/kg of the particulate samples for 4, 18 or 24h. Thereafter, the lungs were lavaged and bronchoalveolar lavage fluid (BALF) was assayed for indicators of inflammation, cytotoxicity and genotoxicity. Lungs of 24h exposed mice were collected for inspection of pulmonary tissue damage. There were substantial differences in the combustion qualities of old and modern technology appliances. Modern technology appliances had the lowest PM₁ (mg/MJ) emissions, but they induced the highest inflammatory, cytotoxic and genotoxic activities. In contrast, old technology appliances had clearly the highest PM₁ (mg/MJ) emissions, but their effect in the mouse lungs were the lowest. Increased inflammatory activity was associated with ash related components of the emissions, whereas high PAH concentrations were correlating with the smallest detected responses, possibly due to their immunosuppressive effect. © 2012 Elsevier B.V.

A mathematical model is developed to simulate synthesis gas production by methane steam reforming process in a fixed bed reactor filled with catalyst particles. Due to the endothermic nature of the reforming reactions heat is supplied into the reactor by means of electrical heating, therefore, the reactor and catalyst particles are exposed to significant axial and radial temperature gradients. A pseudo heterogeneous model is used in order to exactly represent diffusion phenomena inside the reactor tube. Heat and mass transfer equations are coupled with detailed reaction mechanisms and solved for both the flow phase and within the catalyst pellets. The reaction has been investigated from a modeling view point considering the effect of different temperatures ranging from 873 to 1073 (K) on methane conversion and hydrogen yields. The result provides temperature and concentration distribution along the reactor axial and radial coordinates and strong radial temperature gradients particularly close to the entrance of the reactor have been found. © 2013 Elsevier B.V.

Energy systems have increased in complexity in the past years due to the everincreasing integration of intermittent renewable energy sources such as solar thermal or wind power. Modern energy systems comprise different energy domains such as electrical power, heating and cooling which renders their control even more challenging. Employing supervisory controllers, so-called energy management systems (EMSs), can help to handle this complexity and to ensure the energy-efficient and cost-efficient operation of the energy system. One promising approach are optimization-based EMS, which can for example be modelled as stochastic mixed-integer linear programmes (SMILP). Depending on the problem size and control horizon, obtaining solutions for these in real-time is a difficult task. The progressive hedging (PH) algorithm is a practical way for splitting a large problem into smaller subproblems and solving them iteratively, thus possibly reducing the solving time considerably. The idea of the PH algorithm is to aggregate the solutions of subproblems, where artificial costs have been added. These added costs enforce that the aggregated solutions become non-anticipative and
are updated in every iteration of the algorithm. The algorithm is relatively simple to implement in practice, re-using almost all of a possibly existing deterministic implementations and can be easily parallelized.
Although it has no convergence guarantees in the mixed-integer linear case, it can nevertheless be used as a good heuristic for SMILPs. Recent theoretical results shown that for applying augmented Lagrangian functions in the context of mixed-integer programmes, any norm proofs to be a valid penalty function. This is not true for squared norms, like the squared L 2 -norm that is used in the classical progressive hedging algorithm. Building on these theoretical results, the use of the L 1 and L-infinity-norm in the PH algorithm is investigated in this paper. In order to incorporate these into the algorithm an adapted multiplier update step is proposed. Additionally a heuristic extension of the aggregation step and an adaptive penalty parameter update scheme from the literature is investigated. The advantages of the proposed modifications are demonstrated by means of illustrative examples, with the application to SMILP-based EMS in mind.

In cooperation between Vienna University of Technology and Bioenergy 2020+ a project was done which had the objective to evaluate the prospects for the production of Biofuels by integration in existing Austrian biomass industry. The advantages of such integration are the good access to renewable energy resources like wood chips, existing infrastructure for electricity and heat, existing logistics of resources and the utilization of waste heat from Biofuel production to substitute fossil fuels. One work package included the process simulation of thermo-chemical biomass gasification and the production of a second generation Biofuel by the use of Fischer – Tropsch (FT) - synthesis. The process simulation tool IPSEpro was used for the simulation. The simulation of technical processes allows the prediction of the behavior of processes on the base of mathematical models. The quality of a simulation model depends substantially on the used model and the process parameters. The used technologies in the process simulation were the biomass gasification with the Fast Internal Circulating Fluidized Bed (FICFB) – gasification system and the Fischer –Tropsch (FT) - synthesis. The FICFB was developed by the Vienna University of technology. This gasification technology is used in the well known demonstration plant is Güssing (Austria). The produced product gas is nearly nitrogen free and has a high content of hydrogen (45 – 35 Vol%_dry) and carbon monoxide (25 – 20 Vol%_dry). These product gas components are used in the FT - synthesis for the production of FT – raw product. A FT - Trial Plant is also situated in Güssing since the year 2005. A slurry reactor is used in the Trial Plant for the FT – synthesis. The target for the simulation was the production of FT – raw product as well as the substitution of fossil fuels. The waste heat of the process should be used for the production of steam. An amount of 120 tons per hour of fossil produced steam should be substituted. The
Off-Gas of the FT – process was also used for the production of steam. Two different models for location number one were considered. The used fuel was wood chips. The data out of the simulation were used to calculate the economic efficiency of the plants. An important parameter was the price of the FT – raw product per liter. The total costs and the production capacity were set equal to calculate the marginal revenue. Also a sensitivity analysis was done to evaluate the effects of rising fuel costs and increased investment costs.