21. |
- Carlsson, P. T. M., et al.
(author)
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Comparison of isoprene chemical mechanisms under atmospheric night-time conditions in chamber experiments: evidence of hydroperoxy aldehydes and epoxy products from NO3 oxidation
- 2023
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In: Atmospheric Chemistry and Physics. - : Copernicus GmbH. - 1680-7316 .- 1680-7324. ; 23:5, s. 3147-3180
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Journal article (peer-reviewed)abstract
- The gas-phase reaction of isoprene with the nitrate radical (NO3) was investigated in experiments in the outdoor SAPHIR chamber under atmospherically relevant conditions specifically with respect to the chemical lifetime and fate of nitrato-organic peroxy radicals (RO2). Observations of organic products were compared to concentrations expected from different chemical mechanisms: (1) the Master Chemical Mechanism, which simplifies the NO3 isoprene chemistry by only considering one RO2 isomer; (2) the chemical mechanism derived from experiments in the Caltech chamber, which considers different RO2 isomers; and (3) the FZJ-NO3 isoprene mechanism derived from quantum chemical calculations, which in addition to the Caltech mechanism includes equilibrium reactions of RO(2 )isomers, unimolecular reactions of nitrate RO(2 )radicals and epoxidation reactions of nitrate alkoxy radicals. Measurements using mass spectrometer instruments give evidence that the new reactions pathways predicted by quantum chemical calculations play a role in the NO3 oxidation of isoprene. Hydroperoxy aldehyde (HPALD) species, which are specific to unimolecular reactions of nitrate RO2, were detected even in the presence of an OH scavenger, excluding the possibility that concurrent oxidation by hydroxyl radicals (OH) is responsible for their formation. In addition, ion signals at masses that can be attributed to epoxy compounds, which are specific to the epoxidation reaction of nitrate alkoxy radicals, were detected. Measurements of methyl vinyl ketone (MVK) and methacrolein (MACR) concentrations confirm that the decomposition of nitrate alkoxy radicals implemented in the Caltech mechanism cannot compete with the ring-closure reactions predicted by quantum chemical calculations. The validity of the FZJ-NO3 isoprene mechanism is further supported by a good agreement between measured and simulated hydroxyl radical (OH) reactivity. Nevertheless, the FZJ-NO3 isoprene mechanism needs further investigations with respect to the absolute importance of unimolecular reactions of nitrate RO2 and epoxidation reactions of nitrate alkoxy radicals. Absolute concentrations of specific organic nitrates such as nitrate hydroperoxides would be required to experimentally determine product yields and branching ratios of reactions but could not be measured in the chamber experiments due to the lack of calibration standards for these compounds. The temporal evolution of mass traces attributed to product species such as nitrate hydroperoxides, nitrate carbonyl and nitrate alcohols as well as hydroperoxy aldehydes observed by the mass spectrometer instruments demonstrates that further oxidation by the nitrate radical and ozone at atmospheric concentrations is small on the timescale of one night (12 h) for typical oxidant concentrations. However, oxidation by hydroxyl radicals present at night and potentially also produced from the decomposition of nitrate alkoxy radicals can contribute to their nocturnal chemical loss.
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22. |
- Oesterle, Pierre, 1990-
(author)
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Exploring the fate of emerging contaminants during hydrothermal regeneration of carbonaceous adsorbents
- 2023
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Doctoral thesis (other academic/artistic)abstract
- Wastewater from households and industries commonly contain emerging contaminants that are not easily removed by most wastewater treatment plants. These contaminants can be removed through adsorption onto adsorbents, such as activated carbon or biochars. Previously, attention has been given to waste residues from the agriculture and forestry industry as potential raw materials for activated biochars, which could replace coal and coconut, common feedstocks for activated carbon production. This thesis investigates the factors governing the adsorption efficiencies of these activated biochars and explores the potential of hydrothermal regeneration as a post-treatment. The adsorption experiments showed that iron-doped (i.e., magnetic) activated biochar had two times more adsorption capacity than non-doped activated biochar (i.e., non-magnetic). However, the adsorption capacity of magnetic activated biochar was still inferior to activated carbon for removing sulfamethoxazole (8 mg/g vs. 42 mg/g) and caffeine (40 vs. 56 mg/g). Of the three conditions tested (i.e., salts, humic acids, and pH), only pH had a significant influence on the adsorption of the three selected contaminants onto activated biochars, and the biochars preferentially adsorbed neutral species. This observation is most likely explained by the π-π bonds. Hydrothermal regeneration effectively degraded trimethoprim, sulfamethoxazole, and caffeine at temperatures above 240 °C in the absence of adsorbent. Only trimethoprim generated transformation products that could be identified and quantified from non-targeted analysis. In presence of adsorbent, caffeine was not completely degraded at 280 or even 320 °C, suggesting that the activated biochars adsorb and to some extent shelter the contaminants from degradation.After hydrothermal regeneration, the activated biochars had an enhanced adsorption capacity for sulfamethoxazole, whereas lower adsorption capacity was observed for trimethoprim and caffeine. These changes in performance are believed to be related to the alteration of surface characteristics of activated biochar induced by the adsorbed contaminants during the hydrothermal reaction. Overall, the regeneration efficiency for the activated biochars was found to exceed 50 %. After three regeneration cycles, the regeneration efficiency was as high as 320 %. The results of this thesis suggest that activated biochars could remove emerging contaminants in water and hydrothermal regeneration could degrade most of the emerging contaminants, allowing the spent adsorbent to be reused.
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23. |
- Garemark, Jonas, et al.
(author)
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Advancing Hydrovoltaic Energy Harvesting from Wood through Cell Wall Nanoengineering
- 2023
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In: Advanced Functional Materials. - : John Wiley and Sons Inc. - 1616-301X .- 1616-3028. ; 33:4
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Journal article (peer-reviewed)abstract
- Converting omnipresent environmental energy through the assistance of spontaneous water evaporation is an emerging technology for sustainable energy systems. Developing bio-based hydrovoltaic materials further pushes the sustainability, where wood is a prospect due to its native hydrophilic and anisotropic structure. However, current wood-based water evaporation-assisted power generators are facing the challenge of low power density. Here, an efficient hydrovoltaic wood power generator is reported based on wood cell wall nanoengineering. A highly porous wood with cellulosic network filling the lumen is fabricated through a green, one-step treatment using sodium hydroxide to maximize the wood surface area, introduce chemical functionality, and enhance the cell wall permeability of water. An open-circuit potential of ≈140 mV in deionized water is realized, over ten times higher than native wood. Further tuning the pH difference between wood and water, due to an ion concentration gradient, a potential up to 1 V and a remarkable power output of 1.35 µW cm−2 is achieved. The findings in this study provide a new strategy for efficient wood power generators. © 2022 The Authors.
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24. |
- Lindahl, Niklas, 1981, et al.
(author)
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Early stage techno-economic and environmental analysis of aluminium batteries
- 2023
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In: Energy Advances. - : Royal Society of Chemistry (RSC). - 2753-1457. ; 2:3, s. 420-429
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Journal article (peer-reviewed)abstract
- For any proper evaluation of next generation energy storage systems technological, economic, and environmental performance metrics should be considered. Here conceptual cells and systems are designed for different aluminium battery (AlB) concepts, including both active and passive materials. Despite the fact that all AlBs use high-capacity metal anodes and materials with low cost and environmental impact, their energy densities differ vastly and only a few concepts become competitive taking all aspects into account. Notably, AlBs with high-performance inorganic cathodes have the potential to exhibit superior technological and environmental performance, should they be more reversible and energy efficient, while at the system level costs become comparable or slightly higher than for both AlBs with organic cathodes and lithium-ion batteries (LIBs). Overall, with continued development, AlBs should be able to complement LIBs, especially in light of their significantly lower demand for scarce materials. Several aluminium battery concepts are evaluated at material, cell and system levels for technical, economic and environmental performance, which enables them to complement lithium-ion batteries in the future.
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25. |
- Potting, José, et al.
(author)
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Stakeholder participation in sustainability assessment of non-wicked problems: The case of a future seaweed industry in Sweden
- 2021
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In: Ambio. - : Springer Nature. - 0044-7447 .- 1654-7209.
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Journal article (peer-reviewed)abstract
- Acceptance by, and cooperation with relevant stakeholders in developing new sustainability initiatives when they are generally perceived as positive, is one of the keys for successful implementation of such new sustainability initiatives later on. It is remarkable, however, that ample literature exists about involving stakeholders in research projects focusing on problems with diverging views (controversy) around facts and values (wicked problems), but there is very little literature addressing whether and how to involve relevant stakeholders in case of initiatives where diverging norms and values do not play a (substantial) role, like in sustainability assessment for a future seaweed industry. This perspectives paper addresses that gap, and explores how to design such sustainability assessment, illustrated by how stakeholder interaction influenced the assessment and its results for a future seaweed industry in Sweden, followed by a discussion whether and how a similar approach may benefit sustainability assessment of other non-wicked sustainability initiatives.
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26. |
- Carrod, Andrew J., 1994, et al.
(author)
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Recent advances in triplet-triplet annihilation upconversion and singlet fission, towards solar energy applications
- 2022
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In: Energy & Environmental Science. - : Royal Society of Chemistry (RSC). - 1754-5692 .- 1754-5706. ; 15, s. 4982-5016
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Research review (peer-reviewed)abstract
- Solar energy is an ample renewable energy resource, with photovoltaic (PV) technology enabling a direct route from light to electricity. Currently, PVs are limited in photon conversion efficiency, due in major part to spectral losses. Mitigation of these losses is therefore important, economically and environmentally. Two processes that aim to increase solar light utilisation are described herein. The first is triplet-triplet annihilation upconversion (TTA-UC), through which two incoherent photons of low energy can produce one of higher energy, reducing below bandgap losses. Secondly, singlet fission (SF), through which two triplet states may be obtained from one initial singlet excited state, in theory allowing two electrons per photon in a PV, reducing thermalisation losses. These fields are often covered seperately, despite being the reverse processes of one another. This work aims to consolidate research in the two fields and highlight their similarities and common challenges, specifically those relevant to PV applications. Herein, we cover systems primarily based on organic small molecules (anthracene, rubrene, tetracene, pentacene), and detail the fabrication of functional materials containing them (MOFs, gels, SAMs on TiO2, thin evaporated and solution cast films, and cavities). We further offer our recommendations for the focus of future work in both the TTA and SF fields, and discuss the need to address current limitations such as poor triplet diffusion, limited charge injection to PVs, and material stability. Specifically, one could do this by cherry picking ideas from other research fields, for example photosensitisers for photodynamic therapy could be used as TTA sensitisers, and molecules having a considerable excited state aromaticity could be considered as SF materials. We hope this review may aid development towards the end goal of an efficient PV, incorporating either, or both, SF and TTA-UC materials.
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27. |
- Luong, N. Tan, 1995-
(author)
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Water film-mediated mineralogical transformations and photocatalytic reactions
- 2023
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Doctoral thesis (other academic/artistic)abstract
- Mineral particles capture water vapor in the atmosphere in the form of water films that are only few monolayers thick. Water films form nanoscale hydration environments that mediate a wide range of important reactions in nature and technology. This thesis explored two important phenomena that commonly occur within the confines of water films: mineralogical transformations (Topic 1) and photocatalytic decomposition of organics (Topic 2). These transformations were chiefly identified by vibrational spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy and (Transmission and Scanning) electron microscopy. Interpretations of reaction mechanisms were partially supported by chemometrics, kinetic and thermodynamic modeling, as well as molecular simulations.Mineralogical transformations (Topic 1) resolved in this thesis involved the hydroxylation (Papers I, II) and carbonation (Paper III) of periclase (MgO), and the oxidation of rhodochrosite (MnCO3) (Paper IV). Two types of MgO nanocubes with contrasting physical properties were used to resolve nucleation- and diffusion-limited hydroxylation reactions to brucite and carbonation reactions to amorphous magnesium carbonate (AMC). While nucleation-limited reactions completely transformed (8 nm) small and aggregated MgO nanocubes to brucite, the reactions became diffusion-limited in larger (32 nm) monodispersed MgO nanocubes because of brucite surface nanocoatings (Paper I). Additionally, brucite nanosheets grew under (GPa-level) crystallization pressures because of the important volumetric expansion of the reaction, which took place in a complex network of microporosity between the small and within the larger MgO nanocubes. Brucite stacking mechanisms, explored in Paper II, focused on the early stages of MgO-water interaction in water films of different thicknesses. These were suggested to involve the stacking and (epitaxial-like) growth of precursor Mg(OH)2 nanosheets in water films. Carbonation reactions explored in Paper III completely hampered hydroxylation reactions studied in Papers I and II, and produced AMC nanocoatings grown over an unreacted MgO core. Finally, oxidation-driven reactions involving rhodochrosite in Paper IV produced MnO2, Mn3O4, and MnOOH nanocoatings with growth rates being scaled with water loadings.Photocatalytic decomposition reactions of organics (Topic 2) were focused on the case of oxalate bound to TiO2 nanoparticles (Paper V). Photodecomposition rates scaled with humidity in oxygenated water films, and were explained by the combination of hole transfer (HT), ligand-to-metal charge transfer (LMCT), and the formation of hydroxyl radicals and reactive oxygen species. Decreasing rates in oxygen-free water films were, on the other hand, explained by water-driven charge localization, which eventually limited radical production and charge transfers via HT and LMCT. The reactions involved limited HT and LMCT processes which also competed with a charge recombination process across all humidity ranges.This thesis provides new insight into two key types of transformations mediated by water films on minerals. This knowledge can be used to understand the reactivity of mineral (nano)particles exposed to variations in atmospheric humidity and oxygen content, which are both highly relevant to a wide range of settings in nature and technology. It can also advance new ideas in the study of mineral growth, especially within the confines of nanometer-thick water films.
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28. |
- Muangmeesri, Suthawan, 1997-, et al.
(author)
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Recycling of Polyesters by Organocatalyzed Methanolysis Depolymerization : Environmental Sustainability Evaluated by Life Cycle Assessment
- 2024
-
In: ACS Sustainable Chemistry and Engineering. - : American Chemical Society (ACS). - 2168-0485. ; 12:10, s. 4114-4120
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Journal article (peer-reviewed)abstract
- Polyethylene terephthalate (PET) is one of the most common plastics and can be cascaded mechanically during its life cycle. However, recycling affects the mechanical properties of the material, and the virgin material is constantly in demand. If a worn material could be depolymerized to its chemical building blocks, then a virgin polymer could be generated from old fibers. In this work, we have developed a benign organo-catalytic depolymerization of PET to yield dimethyl terephthalate (DMT) and ethylene glycol (EG) without the need for purification of generated monomers. By recirculating the solvent and organo-catalyst, a solvent/substrate ratio of 3:1 was achieved. The depolymerization was successfully applied to other polyesters, polycarbonates, and polycotton. The cotton isolated from the polycotton depolymerization was successfully processed into viscose fibers with a tenacity in the range of nonwaste cotton-derived viscose filaments. The global warming potential (GWP) of PET depolymerization was evaluated by using life cycle assessment (LCA). The GWP of 1 kg PET recycling is 2.206 kg CO2 equivalent, but the process produces DMT, EG, and heat, thereby avoiding the emissions equivalent to 4.075 kg CO2 equivalent from the DMT, EG, and steam-energy production through conventional pathways. Thus, the net result potentially avoids the emission of 1.88 kg of CO2 equivalent. The impact of this process is lower than that of waste PET incineration and conventional PET recycling technologies.
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29. |
- Rocha, Eva, et al.
(author)
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Testing the applicability of dendrochemistry using X-ray fluorescence to trace environmental contamination at a glassworks site
- 2020
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In: Science of the Total Environment. - : Elsevier. - 0048-9697 .- 1879-1026. ; 720, s. 1-12
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Journal article (peer-reviewed)abstract
- The potential of dendrochemistry as a tool for tracing anthropogenic contamination at a glassworks site in southeastern Sweden was investigated through a multidisciplinary approach combining continuous high-resolution time series of tree rings and sediment profiles. Tree cores from Scots pine (Pinus sylvestris), Norway spruce (Picea abies) and European aspen (Populus tremula) were analysed for their elemental composition using an energy dispersive X-ray fluorescence (ED-XRF) technique. Sediment cores were sampled along a transect extending from the pollution point source to unpolluted areas and analysed using core-scanning-XRF (CS-XRF). High contaminant concentrations in the soil were found for As (approximate to 2000 ppm), Pb (>5000 ppm), Ba (approximate to 1000 ppm) and Cd (approximate to 150 ppm). The concentrations decreased with depth and distance from the pollution source. The dendrochemical analyses revealed alterations in the Barium, Chlorine and Manganese profiles, allowing the identification of seven potential asynchronous releases from the glassworks. Our results suggest that differences in the response of tree species to elemental uptake together with soil chemical properties dictate the success of dendrochemistry as an environmental monitoring tool. (C) 2020 Elsevier B.V. All rights reserved.
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30. |
- Hammond, Oliver S., et al.
(author)
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Neutron Diffraction Study of Indole Solvation in Deep Eutectic Systems of Choline Chloride, Malic Acid, and Water
- 2022
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In: Chemistry - A European Journal. - : Wiley. - 0947-6539 .- 1521-3765. ; 28:41
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Journal article (peer-reviewed)abstract
- Deep eutectic systems are currently under intense investigation to replace traditional organic solvents in a range of syntheses. Here, indole in choline chloride-malic acid deep eutectic solvent (DES) was studied as a function of water content, to identify solute interactions with the DES which affect heterocycle reactivity and selectivity, and as a proxy for biomolecule solvation. Empirical Potential Structure Refinement models of neutron diffraction data showed [Cholinium]+ cations associate strongly with the indole π-system due to electrostatics, whereas malic acid is only weakly associated. Trace water is sequestered into the DES and does not interact strongly with indole. When water is added to the DES, it does not interact with the indole π-system but is exclusively in-plane with the heterocyclic rings, forming strong H-bonds with the -NH group, and also weak H-bonds and thus prominent hydrophobic hydration of the indole aromatic region, which could direct selectivity in reactions.
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