Shifting the load demand of a commercial office space to utilise off peak tariffs would lead to cost savings as power is cheaper at this time. To achieve this shift, chemical energy storage was considered using Lead Acid batteries, Lithium-ion batteries and Advance Lead Acid batteries. The output of these storage types is electricity. Current costs of storage do not support the option of reducing peak demand by adding chemical storage, as electricity from the grid is cheaper over the storage project life. A levelised cost analysis was completed and lithium-ion batteries proved to be the outright best choice for chemical storage in commercial office spaces. Town buildings were analysed and assessed for energy savings in order to reduce overall load demand. Incorporating chemical storage as a viable option was assessed based on cost. Heating, Cooling and lighting proved to be the highest load demands in the buildings. Cost savings in buildings can be better met by increasing the efficiency in buildings, rather than by reducing the cost by shifting the purchase of electricity from peak to off-peak tariffs. More suitable options to chemical energy storage would be to replace standard lights with energy efficient variations, installing an air heat pump to heat the space and ice thermal storage to cool the space. The use of a solar thermosyphon will meet the demand for heated water. Solar energy generation was assessed as an alternative as off-peak electricity stored using chemical storage proved to be too costly. A 50kW system would be suitably sized when peak sun hours were above the local areas average. Net metering could be used to offset costs during the winter months, when the peak sun hours fall below the average.

The purpose of this study is to explore how picture books can be used in understanding of chemical processes through teaching practices in pre-schools. More specifically, the study aims to contribute with knowledge about how chemical energy is described and related to in picture books intended for children between 3 and 5 years old. The empirical material consisted of 23 books, which were studied using an inductive approach of content analysis. The result of the study showed that the use of science language was nearly non-existent and in general there were very few mentions of words that could be used to describe chemical energy or processes related to this subject. Researches have demonstrated that the specific science language is used in very specific contexts and is therefore a more difficult language to learn, get knowledge of and use. Previous research has shown that books can be used successfully in teaching, and storytelling has proven to be an effective method for language development. This study has shown that the mediation of knowledge about, and in connection to, chemical energy was presented in a low degree in picture books. For the teacher, this entails the need to bring attention to, describe and mediate knowledge themselves to promote learning in the regarded area. This requires a more conscious approach when using picture books as a pedagogic tool. / Syftet med denna studie är att undersöka hur bilderböcker kan användas för att förklara kemiska energiprocesser i den pedagogiska verksamheten i förskolan. Mer specifikt har studien fokuserat på att bidra med kunskap om hur kemisk energi beskrivs och relateras till i bilderböcker avsedda för barn mellan 3 till 5 år. Det empiriska materialet utgjordes av 23 böcker som har studerats med kvalitativ innehållsanalys med en induktiv ansats. Studiens resultat visade att användandet av ett naturvetenskapligt språk var närmast obefintligt i det studerade materialet och att det generellt var få benämnda ord som användes för att beskriva kemisk energi eller relaterade processer. Det har påvisats av forskare att det naturvetenskapliga språket används i mycket specifika sammanhang och att det därför är svårare att lära, få kunskap om och använda. Tidigare forskning har visat att böcker kan användas framgångsrikt i undervisningen och att högläsning är en effektiv metod för språkutvecklingen. Den här studien har visat att förmedlande av kunskaper inom och relaterade till kemisk energi i låg grad förekommer i bilderböcker. För förskolläraren innebär detta ett behov av att själva uppmärksamma, beskriva och förmedla kunskaperna för att främja lärandet i det berörda området. Detta kräver ett medvetet tillvägagångssätt i användandet av böckerna som ett pedagogiskt verktyg.

<p>Black liquors are presently combusted in recovery boilers where the inorganic cooking chemicals are recovered and the energy in the organic material is converted to steam and electricity. A new technology, developed by Chemrec AB, is black liquor gasification (BLG). BLG has more to offer compared to the recovery boiler process, in terms of on-site generation of electric power, liquid fuel and process chemicals. A prerequisite for both optimization of existing processes and the commercialization of BLG is better understanding of the physical and chemical processes involved including interactions with the refractory lining. The chemistry in the BLG process is very complex and to minimize extensive and expensive time-consuming studies otherwise required accurate and reliable model descriptions are needed for a full understanding of most chemical and physical processes as well as for up-scaling of the new BLG processes. However, by using these calculated model results in practice, the errors in the state of the art thermochemical data have to be considered. An extensive literature review was therefore performed to update the data needed for unary, binary and higher order systems. The results from the review reviled that there is a significant range of uncertainty for several condensed phases and a few gas species. This resulted in experimental re-determinations of the binary phase diagrams sodium carbonate-sodium sulfide (Na2CO3-Na2S) and sodium sulfate-sodium sulfide (Na2SO4-Na2S) using High Temperature Microscopy (HTM), High Temperature X-ray Diffraction (HT-XRD) and Differential Thermal Analysis (DTA). For the Na2CO3-Na2S system, measurements were carried out in dry inert atmosphere at temperatures from 25 to 1200 °C. To examine the influence of pure CO2 atmosphere on the melting behavior, HTM experiments in the same temperature interval were made. The results include re-determination of liquidus curves, in the Na2CO3 rich area, melting points of the pure components as well as determination of the extent of the solid solution, Na2CO3(ss), area. The thermal stability of Na2SO3 was studied and the binary phase diagram Na2SO4-Na2S was re-determined. The results indicate that Na2SO3 can exist for a short time up to 750 °C, before it melts. It was also proved that a solid/solid transformation, not reported earlier, occurs at 675 ± 10 °C. At around 700 °C, Na2SO3 gradually breaks down within a few hours, to finally form the solid phases Na2SO4 and Na2S. From HTM measurements a metastable phase diagram including Na2SO3, as well as an equilibrium phase diagram have been constructed for the binary system Na2SO4-Na2S. Improved data on Na2S was experimentally obtained by using solid-state EMF measurements. The equilibrium constant for Na2S(s) was determined to be log Kf(Na2S(s)) (± 0.05) = 216.28 – 4750(T/K)–1 – 28.28878 ln (T/K). Gibbs energy of formation for Na2S(s) was obtained as ΔfG°(Na2S(s))/(kJ mol–1) (± 1.0) = 90.9 – 4.1407(T/K) + 0.5415849(T/K) ln (T/K). The standard enthalpy of formation of Na2S(s) was evaluated to be ΔfH°(Na2S(s), 298.15 K)/(kJ mol–1) (± 1.0) = – 369.0. The standard entropy was evaluated to be S°(Na2S(s), 298.15 K)/(J mol–1 K–1) (± 2.0) = 97.0. Analyses of used refractory material from the Chemrec gasifier were also performed in order to elucidate the stability of the refractory lining. Scanning electron microscopy (SEM) analysis revealed that the chemical attack was limited to 250-300 μm, of the surface directly exposed to the gasification atmosphere and the smelt. From XRD analysis it was found that the phases in this surface layer of the refractory were dominated by sodiumaluminosilicates, mainly Na1.55Al1.55Si0.45O4.</p>

Black liquors are presently combusted in recovery boilers where the inorganic cooking chemicals are recovered and the energy in the organic material is converted to steam and electricity. A new technology, developed by Chemrec AB, is black liquor gasification (BLG). BLG has more to offer compared to the recovery boiler process, in terms of on-site generation of electric power, liquid fuel and process chemicals. A prerequisite for both optimization of existing processes and the commercialization of BLG is better understanding of the physical and chemical processes involved including interactions with the refractory lining. The chemistry in the BLG process is very complex and to minimize extensive and expensive time-consuming studies otherwise required accurate and reliable model descriptions are needed for a full understanding of most chemical and physical processes as well as for up-scaling of the new BLG processes. However, by using these calculated model results in practice, the errors in the state of the art thermochemical data have to be considered. An extensive literature review was therefore performed to update the data needed for unary, binary and higher order systems. The results from the review reviled that there is a significant range of uncertainty for several condensed phases and a few gas species. This resulted in experimental re-determinations of the binary phase diagrams sodium carbonate-sodium sulfide (Na2CO3-Na2S) and sodium sulfate-sodium sulfide (Na2SO4-Na2S) using High Temperature Microscopy (HTM), High Temperature X-ray Diffraction (HT-XRD) and Differential Thermal Analysis (DTA). For the Na2CO3-Na2S system, measurements were carried out in dry inert atmosphere at temperatures from 25 to 1200 °C. To examine the influence of pure CO2 atmosphere on the melting behavior, HTM experiments in the same temperature interval were made. The results include re-determination of liquidus curves, in the Na2CO3 rich area, melting points of the pure components as well as determination of the extent of the solid solution, Na2CO3(ss), area. The thermal stability of Na2SO3 was studied and the binary phase diagram Na2SO4-Na2S was re-determined. The results indicate that Na2SO3 can exist for a short time up to 750 °C, before it melts. It was also proved that a solid/solid transformation, not reported earlier, occurs at 675 ± 10 °C. At around 700 °C, Na2SO3 gradually breaks down within a few hours, to finally form the solid phases Na2SO4 and Na2S. From HTM measurements a metastable phase diagram including Na2SO3, as well as an equilibrium phase diagram have been constructed for the binary system Na2SO4-Na2S. Improved data on Na2S was experimentally obtained by using solid-state EMF measurements. The equilibrium constant for Na2S(s) was determined to be log Kf(Na2S(s)) (± 0.05) = 216.28 – 4750(T/K)–1 – 28.28878 ln (T/K). Gibbs energy of formation for Na2S(s) was obtained as ΔfG°(Na2S(s))/(kJ mol–1) (± 1.0) = 90.9 – 4.1407(T/K) + 0.5415849(T/K) ln (T/K). The standard enthalpy of formation of Na2S(s) was evaluated to be ΔfH°(Na2S(s), 298.15 K)/(kJ mol–1) (± 1.0) = – 369.0. The standard entropy was evaluated to be S°(Na2S(s), 298.15 K)/(J mol–1 K–1) (± 2.0) = 97.0. Analyses of used refractory material from the Chemrec gasifier were also performed in order to elucidate the stability of the refractory lining. Scanning electron microscopy (SEM) analysis revealed that the chemical attack was limited to 250-300 μm, of the surface directly exposed to the gasification atmosphere and the smelt. From XRD analysis it was found that the phases in this surface layer of the refractory were dominated by sodiumaluminosilicates, mainly Na1.55Al1.55Si0.45O4.

This thesis concerns biogas-operated fuel cells. Fuel cell technology may contribute to more efficient energy use, reduce emissions and also perhaps revolutionize current energy systems. The technology is, however, still immature and has not yet been implemented as dominant in any application or niche market. Research and development is currently being carried out to investigate whether fuel cells can live up to their full potential and to further advance the technology. The research of thesis contributes by exploring the potential of using fuel cells as energy converters of biogas to electricity. The work includes results from four different experimental test facilities and concerns experiments performed at cell, stack and fuel cell system levels. The studies on cell and stack level have focused on the influence of CO, CO2 and air bleed on the current distribution during transient operation. The dynamic response has been evaluated on a single cell, a segmented cell and at stack level. Two fuel cell systems, a 4 kW PEFC system and a 5 kW SOFC system have been operated on upgraded biogas. A significant outcome is that the possibility of operating both PEFCs and SOFCs on biogas has been established. No interruptions or rapid performance loss could be associated with the upgraded biogas during operation. From the studies at cell and stack level, it is clear that CO causes significant changes in the current distribution in a PEFC; air bleed may recover the uneven current distribution and also the drop in cell voltage due to CO and CO2 poisoning. The recovery of cell performance during air bleed occurs evenly over the electrode surface even when the O2 partial pressure is far too low to fully recover the CO poisoning. The O2 supplied to the anode reacts on the anode catalyst and no O2 was measured at the cell outlet for air bleed levels up to 5 %. Reformed biogas and other gases with high CO2 content are thus, from dilution and CO-poisoning perspectives, suitable for PEFC systems. The present work has enhanced our understanding of biogas-operated fuel cells and will serve as basis for future studies. / QC20100708

With growing awareness of global warming and fear of political instability caused by oil depletion, the need for a society with a sustainable energy system has been brought to the fore. A promising technology often mentioned as a key component in such a system is the fuel cell technology, i.e. the energy conversion technology in focus in this thesis. The hopes and expectations on fuel cells are high and sometimes unrealistically positive. However, as an emerging technology, much remains to be proven and the proper use of the technology in terms of suitable applications, integration with society and extent of use is still under debate. This thesis is a contribution to the debate, presenting results from two fuel cell demonstration projects, looking into the introduction of fuel cells on the market, discussing the prospects and concerns for the near-term future and commenting on the potential use in a future sustainable energy system. Bringing fuel cells to reality implies finding near-term niche applications and markets where fuel cell systems may be competitive. In a sense fuel cells are already a reality as they have been demonstrated in various applications world-wide. However, in many of the envisioned applications fuel cells are far from being competitive and sometimes also the environmental benefit of using fuel cells in a given application may be questioned. Bringing reality to fuel cells implies emphasising the need for realistic expectations and pointing out that the first markets have to be based on the currently available technology and not the visions of what fuel cells could be in the future. The results from the demonstration projects show that further development and research on especially the durability for fuel cell systems is crucial and a general recommendation is to design the systems for high reliability and durability rather than striving towards higher energy efficiencies. When reliability and durability are achieved fuel cell systems may be introduced in niche markets where the added values presented by the technology compensate for the initial high cost. / QC 20100909 / Energy Systems Programme / Clean Urban Transport for Europe / GlashusEtt

Continued emission of green house gases has energized research activity worldwide to develop efficient ways to harness renewal energy. The availability of large scale energy storage technologies is essential to make renewal energy a reliable source of energy. Redox flow batteries show potential in this direction. These batteries typically need expensive membranes which need replacement be-cause of fouling. The recently proposed soluble lead redox flow battery (SLRFB), in which lead ions deposit on electrodes in charge cycle and dissolve back in discharge cycle, can potentially cut down the cost of energy storage by eliminating membrane. A number of challenges need to be overcome though. Low cycleability, residue formation, and low efficiencies are foremost among these, all of which require an understanding of the underlying mechanisms. A model of laminar flow-through SLRFB is first developed to understand buildup of residue on electrodes with continued cycling. The model accounts for spatially and temporally growing concentration boundary layers on electrodes in a self consistent manner by permitting local deposition/dissolution rates to be controlled by local ion transport and reaction conditions. The model suggests controlling role for charge transfer reaction on electrodes (anode in particular) and movement of ions in the bulk and concentration boundary layers. The non-uniform current density on electrodes emerges as key to formation of bare patches, steep decrease in voltage marking the end of discharge cycle, and residue buildup with continuing cycles. The model captures the experimental observations very well, and points to improved operational efficiency and decreased residue build up with cylindrical electrodes and alternating flow direction of recirculation. The underlying mechanism for more than an order of magnitude increase in cycle life of a beaker cell battery with increase in stirrer speed is unraveled next. Our experiments show that charging with and without stirring occurs identically, which brings up the hitherto unknown but quite strong role of natural convection in SLRFB. The role of stirring is determined to be dislodgement/disintegration of residue building up on electrodes. The depletion of active material from electrolyte due to residue formation is offset by “internal regeneration mechanism”, unraveled in the present work. When the rate of residue formation, rate of dislodging/disintegration from electrode, and rate of regeneration of active material in bulk of the electrolyte becomes equal, perpetual operation of SLRFB is expected. The identification of strong role of free convection in battery is put to use to demonstrate a battery that requires stirring/mixing only intermittently, during open circuit stages between charge and discharge cycles when no current is drawn. Inspired by our experimental finding that the measured currents for apparently diffusion limited situations (no external flow) are far larger than the maxi-mum possible theoretical value, the earlier model is modified to account for natural convection driven by concentration gradient of lead ions in electrolyte. The model reveals the presence of strong natural convection in battery. The induced flow in the vicinity of the electrodes enhances mass transport rates substantially, to the extent that even in the absence of external flow, normal charge/discharge of battery is predicted. The model predicted electrochemical characteristics are verified quantitatively through voltage-time measurements. The formation of flow circulation loops driven by electrode processes is validated qualitatively through PIV measurements. Natural convection is predicted to play a significant role in the presence of external flow as well. The hitherto unexplained finding in the literature on insensitivity of charge-discharge characteristics to electrolyte flow rate is captured by the model when mixed mode of convection is invoked. Flow reversal and wavy flow are predicted when natural convection and forced convection act in opposite directions in the battery. The effect of the presence of non-conducting material (PbO on anode) on the performance of SLRFB is studied using a simplified approach in the model. The study reveals the presence of charge coup de fouet phenomenon in charge cycle. The phenomenon as well as the predicted effect of depth of discharge on the magnitude of charge coup de fouet are confirmed experimentally.