We briefly review the general concept and expected market potential of microgrids, then discuss the
optimization challenges associated with planning local cross-sectorial energy systems. A fair technology-
neutral approach to this optimization task leads to a hard problem, which has to be tackled with
advanced methods of mathematical optimization.
The power of this approach is illustrated in a case study, concerning the replacement of heating systems
in an alpine valley. In this case study we see both the potential for cost reduction and for the reduction
of CO2 emissions by an integrated planning approach

This research developed a comprehensive computer model for a lab-scale Slurry Bubble Column Reactor (SBCR) (0.1 m D_t and 2.5 m height) for Fischer–Tropsch (FT) synthesis under flexible operation of synthesis gas load flow rates. The variable loads of synthesis gas are set at 3.5, 5, 7.5 m³/h based on laboratory adjustments at three different operating temperatures (483, 493 and 503 K). A set of Partial Differential Equations (PDEs) in the form of mass transfer and chemical reaction are successfully coupled to predict the behavior of all the FT components in two phases (gas and liquid) over the reactor bed. In the gas phase, a single-bubble-class-diameter (SBCD) is adopted and the reduction of superficial gas velocity through the reactor length is incorporated into the model by the overall mass balance. Anderson Schulz Flory distribution is employed for reaction kinetics. The modeling results are in good agreement with experimental data. The results of dynamic modeling show that the steady state condition is attained within 10 min from start-up. Furthermore, they show that step-wise syngas flow rate does not have a detrimental influence on FT product selectivity and the dynamic modeling of the slurry reactor responds quite well to the load change conditions.

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 increased global consumption of chicken products has resulted in the generation of huge amounts of manure. Numerous studies emphasized the large potential of this waste as an untapped source of renewable energy through anaerobic digestion (AD). However, intrinsic difficulties, in particular the high N content, induce instable process conditions, including the accumulation of intermediates, and foaming, which reduces methane yields. Such issues limit the widespread application of this energy-rich substrate for biogas production. The process inhibition by ammonia is usually prevented by reducing the concentration of chicken manure through dilution or by operating the plant considerably below its theoretical reactor capacity. However, this process compromises process efficiency, thereby increasing capital investments and operational costs. Another option to achieve optimal process performance is co-digestion with less N-rich materials. However, co-digestion also has its limitations due to the frequent unavailability of sufficient amounts of C-rich substrates. A series of promising technical solutions have been developed to overcome the aforementioned bottlenecks. Examples include stripping or membrane extraction as means to reduce ammonia concentration in the fermenter. Several full-scale plants employing ammonia removal techniques have been installed recently. Latest research also investigated the use of additives, such as zeolites and trace elements, as well as bioaugmentation, to mitigate ammonia inhibition. The current study reviews the state of technology as well as recent achievements and perspectives. It provides an overview of the different approaches to remove ammonia from AD-process and presents practical examples from China and Europe.

The present study examines the possible use of urban and rural traffic areas for producing biomass. Many of those areas (for example, parking lots at cinemas and shopping centers) are only intensively used during certain times. Most of the time those areas remain empty.
At the same time a major problem for large-scale implementation of renewable energy is the massive land use resulting from limited energy density of solar radiation and, in case of biomass production, low efficiency for utilization of solar radiation by plants. Additionally, renewable energies are often criticized for the fact that they require areas, which could also be used for food and feed production.
Therefore, it is an attractive idea to use some of the traffic areas that are lost for the ecosystem anyway for biomass production. This approach is novel that no data have been available yet. The aim of this work was therefore to develop technical solutions, to quantify the technical potential for this type of biomass production and, subsequently, for energy supply, based on data on the area utilization, climatic data and known properties of microalgae.
The work deals with the question of the technical potential for this approach in Austria. This question is
answered by a survey of the area data in Austria, the elaboration of technical systems for a possible implementation, as well as by calculating the biomass potential, based on simulation results. The data have been collected, analyzed and evaluated in a comprehensive literature search. The potential analysis provides an overview of the distribution of traffic areas in Austria and the resulting biomass potential. Thus, a list of possible areas including biomass and energy quantities is available.

Detailed reaction schemes and experimental data for the online release of pyrolysis volatiles are required to gain a more fundamental understanding of biomass pyrolysis, which would in turn allow the process to be controlled in a more precise way and the development of more targeted applications. A detailed online characterisation of pyrolysis products has been conducted in single particle experiments with spruce pellets at different temperatures, obtaining a good closure of the elemental mass balances. The yields and online release of CO, CO₂, H₂O, CH₄, other light hydrocarbons and total organic condensable species, as well as char yield and composition, can be predicted with a reasonable accuracy with the application of a single particle model, coupled with a detailed pyrolysis scheme, and a simple one-step scheme for tar cracking. In order to achieve it, improvements have been conducted in the pyrolysis scheme, mainly concerning the release of light hydrocarbons and char yield and composition. Deviations are still present in the different groups in which organic condensable species can be classified.

The syngas mixture produced from biomass (bio-syngas) is characterized by a H2/CO molar ratio of 1.5 in this work, which is different from that of traditional syngas ratio of 2. Therefore a hybrid of winddiesel technology with bio-syngas conversion by Fischer–Tropsch synthesis (WD-FT) on a cobalt based catalyst was investigated, for the first time, using a slurry reactor. The result from feeding this technology is compared with the direct converting biomass derived synthetic gas to fuels via Fischer–Tropsch synthesis (BS-FT). Experiments were performed at different syngas composition (variation of H2/CO ratio), keeping the other parameters (temperature 230 °C; gas flow 5 Nm³/h, pressure 20 bar) constant. Comparison of the WD-FT with the BS-FT synthesis results displayed mass fraction of light hydrocarbons and higher catalytic stability and activity after 500 h. The olefin structures for the different product distributions, obtained from different reactions, are determined by ¹H NMR spectroscopy. Negligible amounts of iso-α-olefins were detected in the product of the WD-FT reaction. In the case of the alpha value, a slight change was observed between 0.93 and 0.92 for the BS-FT and WD-FT reaction.
 

In this work a novel reaction mechanism for gas phase reactions has been developed to predict the formation of aromatic compounds from the pyrolysis products of woody biomass particles. The aromatic compounds are important for being main soot precursors as well as their toxic properties. The developed gas phase mechanism is validated with experimental data from literature as well as experimental data performed with a single particle reactor for three different pyrolysis temperatures, namely 550, 800 and 1000°C. A good agreement is achieved between model results and experimental data for the total yield of each main family of aromatic hydrocarbons, i.e. phenolics, BTXs and PAHs.

Adsorptive desulfurization is a promising technology to provide sulfur free fuels for fuel cell based power units. In this work the adsorption kinetics of three different aromatic sulfur heterocycles was studied for Ag-Al₂O₃. The influence of individual as well as competitive adsorption on the selectivity order was investigated by equilibrium and breakthrough experiments. In these experiments a jet-A1 fuel enriched with benzothiophene (BT), dibenzothiophene (DBT), and 4,6-dimethyldibenzothiophene (4,6-DMDBT) was used. The adsorption of aromatic sulfur heterocycles on Ag-Al₂O₃ proceeds via three different adsorption mechanisms. Within these mechanisms the π-interaction (π-Ag) and the direct sulfur-silver interaction (S-Ag) are significantly stronger in comparison to the acid base interaction (S-H). The results showed that the π-Ag and S-Ag interactions are the major adsorption mechanisms in the first stage, where film-diffusion limits the adsorption rate. In the second stage, the S-H interaction plays only an important role for BT, where intraparticle diffusion is the rate controlling step. The overall selectivity order was found to be BT > DBT > 4,6-DMDBT in the case of competitive adsorption for both equilibrium and breakthrough performance. The S-H contribution was related to incorporation of silver into blank γ-alumina, which significantly increased the overall acidity of the adsorbent.

Substitution of fossil fuels for production of electricity, heat, fuels for transportation and chemicals can be realized using biomass steam gasification in a dual fluidized bed (DFB).

Interaction between biomass ash and bed material in a fluidized bed leads to transformation of the bed particle due to enrichment of components from the biomass ash resulting in the development of ash layers on the bed particle surface. These ash-rich particle layers enhance the catalytic activity of the bed material regarding the water-gas-shift reaction and the reduction of tars.

The water-gas-shift reaction at conditions typical for dual fluidized bed biomass gasification at a temperature of 870 °C was investigated. Diffusion and heat transfer limitations were minimized using a lab-scale experimental set-up consisting of a gas mixing section and a quartz glass reactor in which the catalyst is investigated.

Thermochemical conversion of biomass feedstock via dual fluidized bed steam gasification is a well-proven technology used to produce a medium calorific product gas for various applications in the energy or transportation sector or for chemical syntheses. At unfavorable gasification conditions, undesirable high amounts of tar, which are aromatic hydrocarbons, are present in the product gas. High tar contents are a major problem, and they lead to uneconomic operation due to sharply diminished quality of product gas or unexpected plant shut downs due to fouling of the product gas coolers. Currently, tar content is measured with a discontinuous wet-chemical analysis method, which needs several hours of sample preparation to receive the final tar content. The aim of this study is to establish valid correlations between online measured permanent gas components in the product gas and its tar content. The results show that hydrogen, methane, and ethene concentrations are strongly related to the tar content in the product gas, while the carbon monoxide and carbon dioxide content did not show a clear correlation. Using these correlations with online measured gas components provides the possibility of a direct and prompt response of a plant operator in case of unfavorable gasification conditions. Additionally, an optimization of the plant operation can be conducted and thereby, the operation hours and, consequently, the economic efficiency are improved.

This study presents combustion behavior and emission results obtained for different fuels: poultry litter (PL) and its char (PLC), scrap tires (ST) and its char (STC) and blends of char/lignite (PLC/LIG and STC/LIG). The combustion parameters and emissions were investigated via a non-isothermal thermogravimetric method and experiments in a lab-scale reactor. Fuel indexes were used for the prediction of high temperature corrosion risks and slagging potentials of the fuels used. The addition of chars to lignite caused a lowering of the combustion reactivity (anti-synergistic effect). There was a linear correlation between the NO_x emissions and the N content of the fuel. The form of S and the concentrations of alkali metals in the fuel had a strong effect on the extent of SO₂ emissions. The use of PL and PLC in blends reduced SO₂ emissions and sulphur compounds in the fly ash. The 2S/Cl ratio in the fuel showed that only PLC and STC/PLC would show a risk of corrosion during combustion. The ratio of basic to acidic oxides in fuel indicated that ST, STC and STC/LIG have low slagging potential. The molar (Si + P + K)/(Ca + Mg) ratio, which was used for PL, PLC and PLC containing blends, showed that the ash melting temperatures of these fuels would be higher than 1000 °C.

The CO/CO₂ release ratio obtained during char combustion of single biomass particles has been analysed in this work experimentally and by modelling. Experiments have been conducted with spruce, straw and Miscanthus pellets at different temperatures. Furthermore, these experiments have been modelled with a single particle model coupled with a CFD model of the single particle reactor. The results show that the CO/CO₂ ratio strongly depends on the feedstock, being lower for spruce than for straw or Miscanthus. Furthermore, the most commonly employed correlations for this ratio in literature are not adequate, as they either under- or over-predict it.

Dual fluidized bed (DFB) systems for biomass gasification consist of two connected fluidized beds with a circulating bed material in between. Inside such reactor systems, rough conditions occur due to the high temperatures and the movement of the bed material. Computational fluid dynamics calculations are a useful tool for investigating fluid dynamics inside such a reactor system. In this study, an industrial-sized DFB system was simulated with the commercial code CPFD Barracuda. The DFB system is part of the combined heat and power (CHP) plant at Güssing, situated in Austria, and has a total fuel input of 8 MW_th. The model was set up according to geometry and operating data which allows a realistic description of the hot system in the simulation environment. Furthermore, a conversion model for the biomass particles was implemented which covers the drying and devolatilization processes. Homogeneous and heterogeneous reactions were considered. Since drag models have an important influence on fluidization behavior, four drag models were tested. It was found that the EMMS drag model fits best, with an error of below 20%, whereas the other drag models produced much larger errors. Based on this drag law, further simulations were conducted. The simulation model correctly predicts the different fluidization regimes and pressure drops in the reactor system. It is also able to predict the compositions of the product and flue gas, as well as the temperatures inside the reactor, with reasonable accuracy. Due to the results obtained, Barracuda seems suitable for further investigations regarding the fluid mechanics of such reactors.

Firewood roomheaters are popular, widespread and important for reaching European CO₂ emission targets. Since they contribute significantly to local air pollution, they have to be optimized towards minimal emission release, especially in real-life operation. Draught conditions and user behavior, particularly the ignition technique, significantly affect the emission and efficiency performance of firewood roomheaters. This study assessed the effects of the respective parameters experimentally. The results revealed a clear correlation between draught conditions and thermal efficiency. Increased draught conditions up to 48 Pa significantly decreased thermal efficiency by 6%–11% absolutely. However, for gaseous emissions no clear trend was observed. Accordingly, CO and OGC emissions increased at higher draught conditions for one tested roomheater by 30% and 60%, but decreased for two other tested roomheaters by 13%–45%. For PM emissions no effect of increased draught conditions was evident. Top-down ignition technique did not lead to a significant decrease of PM emissions compared to bottom-up ignition. In contrast, bottom-up ignition led to best thermal efficiencies. The use of either spruce or beech as kindling material revealed no significant relevance for the ignition performance.

This study analyses the emission factors of two firewood room heaters under testing conditions which emulate real life operation. A 6.5 kW stove with low heat storage capacity and high leakage rate (stove A) is compared with an 8 kW air-tight stove with high heat storage capacity (stove B). Thermal efficiency, carbon monoxide (CO) and organic gaseous compound (OGC) emissions, as well as the thermal heat losses (THL) during cool down phase were investigated in a series of laboratory tests. Furthermore, the influence of closing the air supply dampers at the end of the heating cycle was evaluated. Test results for the whole test cycle (including cool down phase) showed that stove A had CO emissions of 2633 mg/MJ_Output and OGC emissions of 203 mg/MJ_Output, while stove B had CO emissions of 2408 mg/MJ_Output and OGC emissions of 109 mg/MJ_Output, when air dampers were closed. It was also found that user behaviour has a critical influence on the stoves’ performance. Closing the air supply dampers at the end of the stove operation improved the efficiency by up to 5.0 percentage points. Furthermore, the duration of the cool down phase increased, as well as CO and OGC emissions decreased. As a matter of fact, measures to improve the user behaviour as for example user trainings and accurate manuals are of major importance in order to decrease emissions and increase efficiency of domestic heating appliances. Moreover, real life emission factors of other technologies should be established in order to develop a database which can be applied in air quality dispersion models.

Diffusion coefficients of various solutes in supercritical water, which were either measured or retrieved from Molecular Dynamics simulations, were reviewed. Diffusion coefficients of molecules relevant for supercritical water processes were calculated with correlations reported in the literature and compared to the values of reference data. For conditions well above the critical point of water the simple Stokes-Einstein equation predicts the diffusion coefficients with an accuracy better than 20%. For conditions near the critical point the Wilke-Chang correlation gives the most accurate results. Diffusion coefficients for typical molecules occurring in supercritical water processes such as O2, N2, CO, CO2, or CH4 are estimated to be in the range of 60 · 10⁻⁹ m²/s at 673 K and 30 MPa. For H2, for which no experimental data are available, much higher diffusion coefficients in the range of 250 · 10⁻⁹ m²/s seem plausible. The data set of binary diffusion coefficients in supercritical water, either determined experimentally or by Molecular Dynamics simulations, should be extended significantly to include more solutes, as well as higher temperatures and pressures.
 

In order to evaluate the combustion behaviour of new biomass feedstocks such as short rotation coppice (poplar wood chips), fuels from agriculture (wheat straw pellets) and biomass residues (maize spindle grits), comprehensive test runs investigating both particulate matter (PM) and gaseous emissions were performed. A commercially available small-scale biomass boiler, especially designed to enable high fuel flexibility, was used for this evaluation. The combustion behaviour was determined for various boiler load conditions and primary air ratios while maintaining a constant total air ratio. Based on wet chemical analyses of the fuels, fuel indexes were calculated to deliver primary information on the combustion behaviour to be expected. During the test runs appropriate operating conditions were determined for these new biomass feedstocks in order to optimise combustion parameters and to minimise PM and gaseous emissions as well as to inhibit ash related problems (slagging, ash deposit formation and corrosion). The optimisation of operating conditions by primary measures showed a big potential for a stable boiler operation combined with reduced emissions. The findings provide the basis for a further development of combustion systems as well as control systems for the combustion of new biomass feedstocks.

Most of the hydrogen produced is derived from fossil fuels. Bioenergy2020+ and TU Wien have been working on hydrogen production from biomass since 2009. A pilot plant for hydrogen production from lignocellulosic feedstock was installed onsite using a fluidized bed biomass gasifier in Güssing, Austria. In this work, the behavior of impurities over the gas conditioning stage was investigated. Stable CO conversion and hydration of sulfur components could be observed. Ammonia, benzene, toluene, xylene (BTX) and sulfur reduction could be measured after the biodiesel scrubber. The results show the possibility of using a commercial Fe/Cr-based CO shift catalyst in impurity-rich gas applications. In addition to hydrogen production, the gas treatment setup seems to also be a promising method for adjusting the H₂ to CO ratio for synthesis gas applications.

Steam gasification of solid biomass in dual fluidized bed systems is a suitable technology for the production of chemicals, fuels for transportation, electricity, and district heating. Interaction between biomass ash and bed material leads to the development of Ca-rich bed particle layers. Furthermore, incomplete decomposition of biomass leads to the formation of tar components; among these are stable intermediate products such as 1H-indene and stable gaseous hydrocarbons such as methane. In this work, the influence of bed particle layers on the conversion of intermediate products such as 1H-indene and methane via steam reforming was investigated by conducting experiments in a lab-scale test rig. Satisfying conversion of 1H-indene into gaseous molecules (e.g., CO, CO2, H2) was achieved with used, layered olivine, whereas fresh olivine showed significantly poorer performance. Since steam reforming was connected to the water-gas-shift reaction for the tested hydrocarbons, investigations regarding carbon monoxide conversion in the presence of steam were conducted as well. Furthermore, a comparison of the influence of fresh and used bed material concerning the conversion of methane is presented, showing that methane is not affected by the bed material, independent of the presence of particle layers.
 

The influence of heterogeneous secondary reactions on char oxidation reactivity, which can take place during slow pyrolysis processes in a woody biomass particle, is analyzed in this study. To this end, the oxidative behavior of primary char produced in a thermobalance with initial wood masses of a few milligrams is compared to the behavior of char produced under conditions enhancing secondary reactions, i.e., large particle and bed sizes in fixed-bed reactors. The influence of the maximum conversion temperature, heating rate, and catalytic effect of inorganics is also studied to compare the effect of each parameter. Results show that a significant reduction in reactivity takes place when char is produced under conditions enhancing these secondary reactions during pyrolysis. The effect is of similar order as the effect as a result of thermal annealing at 900 °C or the catalytic effect of alkali and alkaline earth metals. Therefore, the presence of heterogeneous secondary reactions during pyrolysis should be taken into account in studies addressing biomass char reactivity. Furthermore, it is shown that the reduction of reactivity as a result of secondary reactions is related to neither the loss of oxygen-containing functional groups nor the potential blocking of pores, specially micropores, resulting from the formation of this secondary char. The explanation may, therefore, lie on the deactivation or blocking of active sites by the secondary char.

Wood pellet combustion for heating is increasing in importance in Europe. However, the most commonly used heating appliances such as wood pellet stoves are responsible for emissions which could negatively affect human health. The emissions quality of pellet stoves is influenced by pellet properties and combustion phase characteristics. The goal of this study is to investigate the influence of pellet length on the performance of pellets stoves under real life operation conditions. Three softwood pellet samples were produced, differing only in length. Combustion tests with two different types of pellet stoves were performed in steady and non-steady combustion phases. Gaseous and particulate emissions as well as fuel mass flow were measured. Results show a reduced fuel mass flow (up to 36%) into the combustion chamber for long pellets compared to short pellets. The results of the combustion tests show a considerable influence of pellet length on the performance of both pellet stoves. For example, carbon monoxide emissions and particulate emissions of one stove in nominal load operation increased for long pellets compared to short pellets from 185 mg/m³ to 882 mg/m³, and from 27 mg/m³ to 37 mg/m³ respectively. Results also show a considerable influence of the combustion phase on the emissions level.

The energetic utilization of alternative fuels (short rotation coppice, miscanthus), agricultural by-products (straw, corn cobs) or biomass residues (nut shells, coffee grounds) becomes of increasing interest. Due to variations in fuel properties – and the ash content in particular – biomass fuels considerably influence the conditions in the combustion zone and especially in the fuel bed. Usually, state-of-the-art combustion appliances are optimized for a particular fuel quality and typically approved only for utilization of standardized wood pellets or wood chips. Research activities within the GrateAdvance project focus on fuel flexible grate technologies being capable of adapting conditions in the combustion zone by a systematic and targeted adjustment of grate parameters in order to minimize emissions and slagging problems, thus setting the basis for a new generation of biomass technologies. Moreover, a novel control concept will ensure optimal combustion conditions for any biomass fuel, and specifically adjust to relevant fuel properties.

This paper treats the mixing and movement of char in a dual fluidized bed (DFB) biomass gasification plant. In these plants such measurements are troublesome to perform, and so a cold flow model has been developed to investigate this topic. This cold flow model allows simulating the fluidization behaviour of the gasification reactor in the DFB plant in Güssing, Austria. The recirculation of the bed material is also possible, and can be easily controlled with a rotary valve. In the cold flow model, bronze is used as the bed material and polyethylene as the char. It is possible to take samples during operation to investigate the char concentration in the bed material recirculation stream. Experiments have shown that the char shows a flotsam behaviour since it is of low density. Furthermore, the investigations have shown that higher fluidization rates and higher bed material recirculation rates enhance the char mixing and increase the char concentration in the recirculation stream. It was found that doubling the overall char concentration in the system does not lead to a doubling of the char concentration in the bed material recirculation stream. Furthermore, the influence of the bed height in the gasification reactor was investigated. It was found that higher bed heights lead to lower char concentrations in the recirculation stream. These initial investigations revealed that much is still unknown about DFB plants, but the knowledge of the behaviour of the different types of particles in the bubbling bed of the gasification reactor helps to further improve and develop the DFB technology.

The integration of solar thermal plants into district heating grids requires advanced control strategies in order to utilize the full potential in terms of efficiency and least operating effort. State-of-the-art control strategies cannot completely fulfil this since they are not able to consider the physical characteristics of the different components, nor do they take information on future conditions and requirements into account properly. A promising attempt for improvement is the application of model-based control strategies together with practicable forecasting methods for both the solar yield as well as the heat demand. This contribution will present the results of several projects performed on the development of suitable mathematical models, forecasting methods and control strategies relevant for the integration of solar thermal plants into district heating grids.

Primary devolatilization and the exothermic heterogeneous secondary charring of the primary volatiles need to be described in a consistent manner in order to correctly predict the heat of reaction of biomass pyrolysis. Detailed reaction schemes can currently predict mass loss and product composition of biomass pyrolysis with good accuracy, but have a weakness in the description of the heat of reaction. In this work it is shown for the first time that including secondary charring reactions a detailed reaction scheme can predict the evolution of the heat of pyrolysis for different conditions. The enthalpy of reaction is calculated for each reaction as the difference between the net calorific value of reactants and products. The presented model is able to describe the heat evolution in micro-TGA-DSC experiments conducted without a lid, where pyrolysis is endothermic, and with a lid, where secondary reactions are enhanced and the global heat of reaction shifts to exothermic. Furthermore, when it is coupled to a particle model, it correctly describes single particle pyrolysis experiments conducted with beech spheres where there is a remarkably exothermic peak in the centre temperature.

The use of renewable-energy-based heat producers within district heating grids is getting more and more popular. In order to benefit from the advantages and compensate for the different disadvantages of the various types of heat producers powered by renewable energy sources like biomass, solar energy or waste heat, a combination of these systems could be favoured over using, for example, only one main biomass-based boiler. Furthermore , in many cases, the additional use of buffer storages is necessary to fully benefit from the use of these kinds of heat producers. A major challenge with such multi-producer heating grids is the cost optimal management of all heat producers and buffer storages. Therefore , a high-level control strategy is necessary, which is able to plan ahead the use of slowly reacting and/or weather dependent heat producers while minimizing operational costs and pollutant emissions. This article shows the development of a linear model predictive controller (MPC) for a district heating grid with several (renewable) decentralized heat producers and heat storages. In order to provide the MPC with the required forecast of the future heat demand, an adaptive load forecasting method has been designed. Additionally, in order to be able to incorporate solar panels, the MPC needs to have a forecast of their possible future heat output. Therefore, a physically motivated solar yield forecasting method has been designed. The required prediction models for the MPC were represented by so-called mixed logical dynamical (MLD) system models. MLD system models combine the modelling power of discrete state system models (finite state machines) and discrete time system models by the extension of the regular linear state-space system model approach with integer and continuous auxiliary variables and linear inequality constraints. The occurrence of both integer and continuous variables within the resulting optimization problem of the MPC leads to a mixed-integer linear program (MILP), which can be solved efficiently using modern MILP solvers. The resulting control strategy is tested in a thermo-hydraulic simulation environment of an actual small-scale multi-producer district heating grid consisting of a medium-scale wood chip boiler with buffer storage, a solar collector with buffer storage and a high temperature heat pump, an oil boiler and 25 heat consumers. Additionally, a state observer was designed and connected with the MPC in order to detect control errors and to incorporate feedback from the heat producers and the buffer storages. The simulations have indicated that the designed MPC and the state observer work properly. Therefore, these elements have been implemented on-site on the actual heating grid, with the first test run scheduled for October 2017.
Modellprädiktive Regelung eines solar-und biomassebasierten Fernwärmenetzes | Request PDF. Available from: https://www.researchgate.net/publication/321314304_Modellpradiktive_Regelung_eines_solar-und_biomassebasierten_Fernwarmenetzes [accessed Feb 21 2018].

Toxicological characterisation of combustion emissions in vitro are often conducted with macrophage cell lines, and the majority of these experiments are based on responses measured at 24 h after the exposure. The aim of this study was to investigate how significant role time course plays on toxicological endpoints that are commonly measured in vitro. The RAW264.7 macrophage cell line was exposed to PM₁ samples (150 μg/ml) from biomass combustion devices representing old and modern combustion technologies for 2, 4, 8, 12, 24 and 32 h. After the exposure, cellular metabolic activity, cell membrane integrity, cellular DNA content, DNA damage and production of inflammatory markers were assessed. The present study revealed major differences in the time courses of the responses, statistical differences between the studied samples mostly limiting to differences between modern and old technology samples. Early stage responses consisted of disturbances in metabolic activity and cell membrane integrity. Middle time points revealed increases in chemokine production, whereas late-phase responses exhibited mostly increased DNA-damage, decreased membrane integrity and apoptotic activity. Altogether, these results implicate that the time point of measurement has to be considered carefully, when the toxicity of emission particles is characterised in in vitro study set-ups.

In this paper, the performance of a water gas shift unit processing product gas from a commercial dual fluidised bed biomass steam gasification plant is studied. The experiments were carried out during a partial load operation of the gasification plant. In order to investigate a water gas shift process, a water gas shift unit, located at the site of the gasification plant in Oberwart, Austria, was used. The water gas shift unit consisted of three reactors in series filled with a commercial Fe'Cr-based catalyst and was operated with tar-rich product gas. No performance decrease of the water gas shift unit was observed during the partial load operation of the gasification plant. Furthermore, a CO conversion of 92% and a GCMS tar reduction of about 30% were reached. In addition, it was found that partial load operation of the gasification plant did not negatively affect the performance of the water gas shift unit.

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.

Adsorptive on-board desulfurization units require a high desulfurization and regeneration performance for a wide range of fuels to keep them small and ensure long maintenance intervals. A novel thermal regeneration strategy was investigated in this work, fulfilling all requirements for in situ on-board regeneration. In this strategy, a temperature-controlled flow rate (TCFR) of air was used to control the temperature inside the adsorber. With this dynamic approach, the regeneration time was reduced significantly in comparison to other thermal regeneration strategies. The novel regeneration strategy was tested using Ag–Al₂O₃ as an adsorbent to desulfurize a benzothiophen (BT)-enriched road diesel (300 ppmw of total sulfur). A commercial diesel containing fatty acid methyl ester (FAME) was used to evaluate the fuel flexibility regarding desulfurization and regeneration performance. In the case of 6.63 wt % FAME and 300 ppmw of sulfur, the breakthrough adsorption capacity of sulfur decreased from 1.04 to 0.17 mg/g. In TCFR regeneration experiments, the breakthrough adsorption capacity was restored to over 94% in the case of both fuels. Thereby, the Brunauer–Emmett–Teller (BET) surface area of the regenerated adsorbent decreased by only 1.5%, and negligible carbon deposits were detected.