This publication focuses on the experimental investigation of a novel small-scale fuel flexible biomass combustion technology with a fixed-bed employing a low oxygen concentration. It was obtained through a low primary air ratio and the additional supply of recirculated flue gas. The plant was operated with spruce wood chips, which contained three different mass fractions of water, and miscanthus pellets. All relevant components of the released gas above the fixed-bed were measured, as well as the 3D bed temperature distribution. The balances confirmed a high experimental data consistency. Therefore, it was possible to determine the location of the four different conversion zones inside the fixed-bed: drying, pyrolysis, char gasification and char oxidation. The reduction of CO2 to CO in the char reduction zone worked efficiently across the entire grate area. Furthermore, the results showed that the water mass fraction of the fuel did not influence the dry product gas composition, but significantly affected the location for the release of pyrolysis products such as tars. It was found that the low oxygen concentration in the fixed-bed combined with flue gas recirculation was an effective method to reduce bed temperatures and therefore its inorganic emissions while significantly increasing feedstock flexibility. The investigations provided fundamental findings on the conversion and release behavior of the new technology under real operating conditions and are very useful for further experimental work and CFD simulations targeting the reduction of PM and NOX emissions.

Biomass has the potential to make a major contribution to a renewable future economy. If biomass is gasified, a wide variety of products (e.g., bulk chemicals, hydrogen, methane, alcohols, diesel) can be produced. In each of these processes, gas cleaning is crucial. Impurities in the gas can cause catalyst poisoning, pipe plugging, unstable or poisoned end products, or harm the environment. Aromatic compounds (e.g., benzene, naphthalene, pyrene), in particular, have a huge impact on stable operation of syngas processes. The removal of these compounds can be accomplished by wet, dry, or hot gas cleaning methods. Wet gas cleaning methods tend to produce huge amounts of wastewater, which needs to be treated separately. Hot gas cleaning methods provide a clean gas but are often cost intensive due to the high operating temperatures and catalysts used in the system. Another approach is dry or semi-dry gas cleaning methods, including absorption and adsorption on solid matter. In this work, special focus was laid on adsorption-based gas cleaning for syngas applications. Adsorption and desorption test runs were carried out under laboratory conditions using a model gas with aromatic impurities. Adsorption isotherms, as well as dynamics, were measured with a multi-compound model gas. Based on these results, a temperature swing adsorption process was designed and tested under laboratory conditions, showing the possibility of replacing conventional wet gas cleaning with a semi-dry gas cleaning approach.

Control strategies of absorption heat pumping systems (AHPS, comprising heat pumps and chillers) often
perform insufficiently well, since they usually do not explicitly consider the systems’ dynamics and crosscoupling effects. One promising approach to improve their performance is to apply model-based control strategies since they would allow for an explicit consideration of these system characteristics. Therefore, mathematically simple models of the system to be controlled are required. This contribution proposes a new approach for such a model for a H2O-LiBr AHPS. The model results from the linearization of a more complex, nonlinear simulation model, leading to a simple, but physically still meaningful linear state-space model structure. The experimental validation shows that the developed model describes the system’s dynamics and cross-coupling effects sufficiently well and indicates that it is suitable to serve as a basis for the development of a model-based control strategy for AHPS.

Absorptionskälteanlagen können einen wesentlichen Beitrag zur Verringerung von CO2-Emissionen leisten, wenn Wärme aus regenerativen Energieträgern oder Abwärme aus industriellen Prozessen zum Antrieb verwendet wird. Absorptionskälteanlagen weisen bereits jetzt eine hohe Effizienz auf, bei veränderlichen Betriebsbedingungen kann diese je nach vorhandenen Stellgliedern weiter gesteigert werden. Dazu werden im Rahmen des Forschungsprojektes „Heat Pumping Systems Control (HPC)“ zwei Absorptionskälteanlagen – eine mit der Stoffpaarung Ammoniak/Wasser (NH3/H2O) und eine mit der Stoffpaarung Wasser/Lithiumbromid (H2O/LiBr) – untersucht, um für unterschiedliche Anwendungen optimale Betriebsstrategien zu entwickeln. Zur Berücksichtigung der Zustandsänderungen in der Absorptionskälteanlage, werden dynamische Simulationsmodelle in der Modellierungssprache Modelica entwickelt und mit Messdaten validiert.

Im Rahmen dieses Konferenzbeitrags werden Komponentenmodelle für die NH3/H2O-Absorptionskälteanlage und Simulationsrechnungen bei veränderlichen Randbedingungen präsentiert, sowie ein Vergleich mit Messdaten diskutiert.

Pyrolysis conditions in charcoal production affect yields, properties, and further use of charcoal. Reactivity is a critical property when using charcoal as an alternative to fossil coal and coke, as fuel or reductant, in different industrial processes. This work aimed to obtain a holistic understanding of the effects of pyrolysis conditions on the reactivity of charcoal. Notably, this study focuses on the complex effects that appear when producing charcoal from large biomass particles in comparison with the literature on pulverized biomass. Charcoals were produced from woodchips under a variety of pyrolysis conditions (heating rate, temperature, reaction gas, type of biomass, and bio-oil embedding). Gasification reactivity of produced charcoal was determined through thermogravimetric analysis under isothermal conditions of 850 °C and 20% of CO2. The charcoals were characterized for the elemental composition, specific surface area, pore volume and distribution, and carbon structure. The analysis results were used to elucidate the relationship between the pyrolysis conditions and the reactivity. Heating rate and temperature were the most influential pyrolysis parameters affecting charcoal reactivity, followed by the reaction gas and bio-oil embedding. The effects of these pyrolysis conditions on charcoal reactivity could primarily be explained by the difference in the meso- and macropore volume and the size and structural order of aromatic clusters. The lower reactivity of slow pyrolysis charcoals also coincided with their lower catalytic inorganic content. The reactivity difference between spruce and birch charcoals appears to be mainly caused by the difference in catalytically active inorganic elements. Contrary to pyrolysis of pulverized biomass, a low heating rate produced a higher specific surface area compared with a high heating rate. Furthermore, the porous structure and the reactivity of charcoal produced from woodchips were influenced when the secondary char formation was promoted, which cannot be observed in pyrolysis of pulverized biomass.

Four different models for heat transfer to the particles immersed in a fluidized bed were evaluated and implemented into an existing single particle model. Pyrolysis experiments have been conducted using a fluidized bed installed on a balance at different temperatures and fluidization velocities using softwood pellets. Using a heat transfer model applicable for fluidized beds, the single particle model was able to predict the experimental results of mass loss obtained in this study as well as experimental data from literature with a reasonable accuracy. A good agreement between experimental and modeling results was found for different reactor temperatures and configurations as well as different biomass types, particle sizes – in the typical range of pellets - and fluidization velocities when they were higher than . However, significant deviations were found for fluidization velocities close to minimum fluidization. Heat transfer models which consider the influence of fluidization velocity show a better agreement in this case although differences are still present.

The majority of renewable energy technologies are volatile in nature. External factors such as weather conditions lead to fluctuations in their produced electricity and heat. This results in a demand either not being covered or dissatisfied since too much electricity and heat is produced in the energy system. Although energy storages can counteract these fluctuations, renewable energy technologies that are capable of producing energy on demand are needed as well. As such, technologies based on the thermochemical conversion of biomass are especially relevant as they are considered to be CO2-neutral. Although most existing implementations are based on combustion of biomass, fixed-bed biomass gasification is of growing relevance due to higher overall efficiencies and low pollutant emissions. Currently, fixed-bed biomass gasifiers are usually operated at steady-state operation to produce the maximum amount of energy possible. This contribution investigates, whether they can be used as a technology for demand-oriented electricity and heat production

The operation characteristics of thermally driven absorption refrigeration systems (ARS) are strongly dependent on their hydraulic integration. Therefore, varying operating conditions of the hydraulic supply have a great influence on the behaviour of ARS and lead to dynamic operation, which can affect the efficiency and is largely unexplored so far. To enable a simple investigation of ARS integration considering their dynamic behaviour and to develop modern, efficiency-enhancing control strategies, dynamic simulation models of ARS are developed in Modelica Code.

In this paper, a dynamic simulation model of an ARS with the working pair ammonia/water (NH3/H2O) is presented. The parameterization and the physical correlations of selected components of the simulation model are described. Afterwards, the simulation model is verified by comparing simulation results with measurement data of the NH3/H2O-ARS. Finally, the capabilities of the simulation model are demonstrated by performing a simulation-based analysis of the temperature glide of the refrigerant in the evaporator.

This study aims to determine the fate of P during fluidized bed co-combustion of chicken litter (CL) with K-rich fuels [e.g., wheat straw (WS)] and Ca-rich fuels (bark). The effect of fuel blending on phosphate speciation in ash was investigated. This was performed by chemical characterization of ash fractions to determine which phosphate compounds had formed and identify plausible ash transformation reactions for P. The ash fractions were produced in combustion experiments using CL and fuel blends with 30% CL and WS or bark (B) at 790–810 °C in a 5 kW laboratory-scale bubbling fluidized bed. Potassium feldspar was used as the bed material. Bed ash particles, cyclone ash, and particulate matter (PM) were collected and subjected to chemical analysis with scanning electron microscopy–energy-dispersive X-ray spectrometry (SEM–EDS) and X-ray diffraction. P was detected in coarse ash fractions only, that is, bed ash, cyclone ash, and coarse PM fraction (>1 μm); no P could be detected in the fine PM fraction (<1 μm). SEM–EDS analysis showed that P was mainly present in K–Ca–P-rich areas for pure CL as well as in the ashes from the fuel blends of CL with WS or B. In the WS blend, P was found together with Si in these areas. The crystalline compound containing P was hydroxyapatite in all cases as well as whitlockite in the cases of pure CL and WS blend, of which the latter compound has been previously identified as a promising plant nutrient. The ash fractions from CL and bark blend only contained P in hydroxyapatite. Co-combustion of CL together with WS appears to be promising for P recovery, and ashes with this composition could be further studied in plant growth experiments

Interaction of biomass ash and bed materials in thermochemical conversion in fluidized beds leads to changes of the bed particle surface due to ash layer formation. Ash components present on the bed particle surface strongly depend on the ash composition of the fuel. Thus, the residual biomass used has a strong influence on the surface changes on bed particles in fluidized bed conversion processes and, therefore, on the catalytic performance of the bed material layers. Ash layer formation is associated with an increase in the catalytic activity of the bed particles in gasification and plays a key role in the operability of different biomass fuels. The catalytic activation over time was observed for K-feldspar used as the bed material with bark, chicken manure, and a mixture of bark and chicken manure as fuels. The changes on the bed material surfaces were further characterized by SEM/EDS and BET analyses. Raman, XPS, and XRD analyses were used to characterize the crystal phases on the bed material surface. An increase in surface area over time was observed for K-feldspar during the interaction with biomass ash. Additionally, a more inhomogeneous surface composition for fuels containing chicken manure in comparison to pure bark was observed. This was due to the active participation of phosphorus from the fuel ash in the ash transformation reactions leading to their presence on the particle surface. A decreased catalytic activity was observed for the same BET surface area compared to bark combustion, caused by the different fuel ash composition of chicken manure.