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Fig.7 shows the influence of the mass ratio on the thermodynamic efficiency of different TSHS cycles. Fig.8 depicts the influence of the mass ratio on the thermal energy storage density of different TSHS cycles. Fig.9 indicates the influence of the conversion rate on the thermodynamic efficiency of different TSHS cycles. Fig.10 represents the influence of the conversion rate on the thermal energy storage density of different TSHS cycles. The data files correspond to abovementioned figures.

This data is connected to the research paper "Arctic geese tune migration to a warming climate but still suffer from a phenological mismatch". It includes data on migration and reproduction timing of Barnacle Geese in relation to the timing of snow melt and plant phenology, and also reproduction data from Barnacle Geese. Detailed information can be found in the README file. Please contact me before using these data.

Practitioners frequently use ecological designed semantic on packaging to provide consumers with information about the environmental quality of the product itself. However, discrepancies between packaging cues and actual pro-environmental product quality trigger confusion and mistrust regarding organic products (i.e., “greenwashing” a conventional product with ecological semantics, “conventional-washing” an organic product with conventional semantics”). This study sought to understand whether (nonverbal) ecological packaging semantics would equate to increases in attributed environmental product quality; the persuasiveness of nonverbal packaging design media (i.e., visual, material), effects on further quality attributions and marketing-relevant variables (e.g., trustworthiness, willingness to pay) and the influence of consumers’ environmental consciousness levels. Findings indicate robust spillover effects of ecological design communications on a product's perceived environmental friendliness, which in turn was correlated to further quality attributions and marketing-relevant variables (e.g., trustworthiness, willingness to pay). Moreover, individuals’ environmental consciousness (EC) showed as a relevant moderating variable, with spillover effects being more pronounced for individuals with rather low EC.

In this article, we have developed a formal optimization paradigm to find loading configurations of dry cask storage over the reactor lifetime. We also developed a new methodology for solving the problem based on state-of-the-art metaheuristic algorithms. The new method was demonstrated using the case of the Vermont Yankee Nuclear Power Station, and the results from the method were evaluated against an “oldest and coldest” loading strategy.

In this article, we have developed a formal optimization paradigm to find loading configurations of dry cask storage over the reactor lifetime. We also developed a new methodology for solving the problem based on state-of-the-art metaheuristic algorithms. The new method was demonstrated using the case of the Vermont Yankee Nuclear Power Station, and the results from the method were evaluated against an “oldest and coldest” loading strategy.

The optical and photovoltaic properties of Si NCs / SiC multilayers (MLs) are investigated using a membrane-based solar cell structure. By removing the Si substrate in the active cell area, the MLs are studied without any bulk Si substrate contribution. The occurrence is confirmed by scanning electron microscopy and light-beam induced current mapping . Optical characterization combined with simulations allows us to determine the absorption within the ML absorber layer, isolated from the other cell stack layers. The results indicate that the absorption at wavelengths longer than 800 nm is only due to the SiC matrix. The measured short-circuit current is significantly lower than that theoretically obtained from absorption within the ML absorber, which is ascribed to losses that limit carrier extraction. The origin of these losses is discussed in terms of the material regions where recombination takes place. Our results indicate that carrier extraction is most efficient from the Si NCs themselves, whereas recombination is strongest in SiC and residual a-Si domains . Together with the observed onset of the external quantum efficiency (EQE) at 700-800 nm, this fact is an evidence of quantum confinement in Si NCs embedded in SiC on device level.

Ammonia has been responsible for feeding population growth in the 20th century through synthetic fertilizer, and is poised to become the preferred energy storage medium for a society powered by renewable electricity in the 21st century. However, conventional brown ammonia production through the Haber-Bosch process is optimized for utilization of centralized and steady energy supply from fossil-fuels. When shifting to distributed and intermittent energy supply through wind and solar energy, a re-optimization is required for a low-capital and flexible green ammonia production processes. This thesis re-designs and Haber-Bosch process by targeting the integration of reaction and separation in a single process vessel at low pressures, thereby achieving the simplification and down-scaling of the high pressure recycle loop of the Haber-Bosch process. Materials are developed for this purpose, the feasibility of integration is demonstrated, and mathematical modeling is utilized for assessing the application of the single-vessel process to a range of renewable energy sources in comparison to competing ammonia production processes. Herein, a catalyst with low-temperature (< 350°C) and high-conversion (i.e. near equilibrium) activity is developed using ruthenium nanoparticles as the active metal supported on ceria and promoted with cesium to mitigate hydrogen and ammonia inhibition, respectively. This catalyst is compared to commercial iron-based catalyst from the perspective of the final application. Concurrently, a high-temperature (> 300°C) manganese chloride absorbent is developed that resists decomposition and is stable when supported on silica. These catalyst and absorbent are integrated in a layered reactor configuration to demonstrate the feasibility of the integrated process by exceeding single-pass reaction equilibrium. Mathematical modelling of ammonia production processes illustrates that at small-scales (< 1 t day-1) the single-vessel process is optimal compared to the Haber-Bosch process due to its modular design. In addition, it can achieve simpler ramping because the Haber-Bosch process is constrained by heat-integration in the recycle loop and the potential for runaway reaction. For final application, the pairing of ammonia production processes with examples of intermittent solar and wind sources demonstrates that the flexibility of the production process is essential when considering non-ideal sources of energy with a long-term (e.g. seasonal) oscillations. Flexible ammonia production also expands the economic usage of ammonia as an energy storage vector from the seasonal to the weekly time-scale, with advantage compared to batteries or hydrogen. The work of this thesis provides a framework for advancing the electrification of the chemical industry given the novel constrains of intermittent and distributed renewable energy. A systems level approach is applied from the ground up, starting from material design and progressing to optimized process design and application.

The aggravating global problems of energy crisis, rising atmospheric greenhouse gas concentrations and accumulation of persistent waste have attracted the attention of scientists, policy-makers and global organisations to come up with effective and expeditious solutions to address these challenges. In this context, the development of sustainable technologies driven by renewable energy sources for the production of clean fuels and commodity chemicals from diverse waste feedstocks is an appealing approach towards creating a circular economy. Over the years, semiconductor photocatalysts based on TiO₂, CdS, carbon-nitrides (CNx) and carbon dots (CDs) have been widely used for the photocatalytic reforming (PC reforming) of pre-treated waste substrates to organic products, accompanied with clean hydrogen (H₂) generation. However, these conventional solar-driven processes suffer from major drawbacks such as low production rates, poor product selectivity, CO₂ release, challenging process and catalyst optimisation, and harsh waste pre-treatment conditions, which limit their commercial applicability. These challenges are tackled in this thesis with the introduction of new and efficient photoelectrochemical (PEC) and chemoenzymatic processes for reforming a diverse range of waste feedstocks to sustainable fuels. Solar-driven PEC reforming based on halide perovskite light-absorber is first developed as an attractive alternative to PC reforming. The PEC systems consist of a perovskite|Pt photocathode for clean H₂ production and a Cu-Pd alloy anode for reforming diverse waste streams, including pre-treated cellulosic biomass, polyethylene terephthalate (PET) plastics, and industrial by-product glycerol into industrially-relevant, value-added chemicals (gluconic acid, glycolic acid and glyceric acid) without any externally applied bias or voltage. Additionally, the single light-absorber PEC systems can also convert the airborne waste stream and greenhouse gas CO₂ to diverse products with the simultaneous reforming of PET plastics with no applied voltage. The perovskite-based photocathode enables the integration of different CO₂ reduction catalysts such as a molecular cobalt porphyrin, a Cu-In alloy and formate dehydrogenase enzyme, which produce CO, syngas and formate, respectively. The versatile PEC systems, which can be assembled in either a ‘two-compartment’ or standalone ‘artificial leaf’ configurations achieve 60‒90% oxidation product selectivity (with no over-oxidation) and >100 µmol cm‾² h‾¹ product formation rates, corresponding to 10²‒10⁴ times higher activity than conventional PC reforming systems. In addition to developing PEC platforms, this thesis also explores avenues for circumventing the harsh alkaline pre-treatment strategies (pH >13, 60‒80 ºC) adopted for photoreforming waste substrates. For this purpose, a chemoenzymatic pathway is introduced whereby PET and polycaprolactone plastics were deconstructed using functional enzymes under benign conditions (pH 6‒8, 37‒65 ºC), followed by PC reforming using Pt loaded TiO₂ (TiO₂|Pt) or Ni₂P loaded carbon-nitride (CNx|Ni₂P) photocatalysts. The chemoenzymatic reforming process demonstrates versatility in upcycling polyester films and nanoplastics for H₂ production at high yields reaching ∼10³‒10⁴ µmol gsub‾¹ and activities at >500 µmol gcat‾¹ h‾¹. The utilisation of enzyme pre-treated plastics also allowed the coupling of plastic reforming with photocatalytic CO₂-to-syngas conversion using a phosphonated cobalt bis(terpyridine) co-catalyst immobilised on TiO₂ (TiO₂|CotpyP). Finally, moving beyond solar-driven systems, a bio-electrocatalytic flow process is demonstrated for the conversion of microbe pre-treated food waste to ethylene (an important feedstock in the chemical industry) on graphitic carbon electrodes via succinic acid as the central intermediate. In conclusion, with its focus on improving efficiencies, achieving selective product formation, building versatile platforms, diversifying substrate and product scope, and reducing carbon footprint and economic strain, this thesis aims to bring sustainable waste-to-fuel technologies a step closer to commercial implementation.

The production of charcoal for its many uses requires a careful selection of biomass and pyrolysis conditions, especially temperature, to ensure suitable quality. To do so, physical, chemical, and mechanical energy must be considered. This study aimed to analyze the yields and properties of charcoal produced at different pyrolysis temperatures. Eucalyptus saligna wood was pyrolyzed in a reactor with final temperatures of 450, 550, 650, 750, 850 and 950 °C. The yields of charcoal, pyroligneous liquid and non-condensable gases were determined. Mass loss was determined for each temperature. Charcoal analysis included the determination of the apparent density, proximate analysis, heating value, mechanical strength, X-ray images for the internal visualization of its structure and hygroscopicity test. Relevant charcoal properties for the steel industry and barbecue, such as density, mechanical strength, heating value and hygroscopicity, show variable trends from pyrolysis at 650 °C. The results show that pyrolysis temperature had a great impact on the properties of charcoal. The apparent density of charcoal rose from 500 °C and had no relation to the breaking strength. When the pyrolysis temperature was raised, an increase in both apparent and true densities, internal fissures and cracks and fixed carbon content of charcoal was observed.