In the first part of this work a novel type of low-density, sponge-like material for the separation of mixtures of oil and water has been prepared by vapour deposition of hydrophobic tri-chloro-silanes on ultra-porous cellulose nanofibril (CNF) aerogels. To achieve this, a highly porous (&gt;99%) robust CNF aerogel with high structural flexibility is first formed by freeze-drying an aqueous suspension of the CNFs. The density, pore size distribution and wetting properties of the aerogel can be tuned by selecting the concentration of the CNF suspension before freeze-drying. The hydrophobic light-weight aerogels are almost instantly filled with the oil phase when they selectively absorb oil from water, with a capacity to absorb up to 45 times their own weight. The oil can subsequently be drained from the aerogel and the aerogel can then be subjected to a second absorption cycle. The second part is about aerogels with different pore structures and manufactured with freeze-drying and supercritical carbon dioxide for the preparation of super slippery surfaces. Tunable super slippery liquid-infused porous surfaces (SLIPS) were fabricated through fluorination of CNFsand subsequent infusion with perfluorinated liquid lubricants. CNF-based self-standing membranes repelled water and hexadecane with roll-off angles of only a few degrees. The lifetime of the slippery surface was controlled by the rate of evaporation of the lubricant, where the low roll-off angle could be regained with additional infusion. Moreover, adjusting the porosity of the membranes allowed the amount of infused lubricant to be tuned and thereby the lifetime. The CNF-based process permitted the expansion of the concept to coatings on glass, steel, paper and silicon. The lubricant-infused films and coatings are optically transparent and also feature self-cleaning and self-repairing abilities. The third part describes how porous structures from CNFs can be prepared in a new way by using a Pickering foam technique to create CNF-stabilized foams. This technique is promising for up-scaling to enable these porous nanostructured cellulose materials to be produced on a large scale. With this technique, a novel, lightweight and strong porous cellulose material has been prepared by drying aqueous foams stabilized with surface-modified CNFs. Confocal microscopy and high-speed video imaging show that the long-term stability of the wet foams can be attributed to the octylamine-coated, rod-shaped CNF nanoparticles residing at the air-liquid interface which prevent the air bubbles from collapsing or coalescing. Careful removal of the water yields a porous cellulose-based material with a porosity of 98 %, and measurements with an autoporosimeter (APVD) reveal that most pores have a radius in the range of 300 to 500 μm. In the fourth part, the aim was to clarify the mechanisms behind the stabilizing action of CNFs in wet-stable cellulose foams. Factors that have been investigated are the importance of the surface energy of the stabilizing CNF particles, their aspect ratio and charge density, and the concentration of CNF particles at the air-water interface. In order to investigate these parameters, the viscoelastic properties of the interface have been evaluated using the pendant drop method. The properties of the interface have also been compared by foam stability tests to clarify how the interface properties can be related to the foam stability over time. The most important results and conclusions are that CNFs can be used as stabilizing particles for aqueous foams already at a concentration as low as 5 g/L. The reasons for this are the high aspect ratio which is important for gel formation and the viscoelastic modulus of the air-water interface. Foams stabilized with CNFs are therefore much more stable than foams stabilized by cellulose nanocrystals (CNC). The charge density of the CNFs affects the level of liberation of the CNFs within large CNF aggregates and hence the number of contact points at the interface, and also the gel formation and viscoelastic modulus. The charges also lead to a disjoining pressure related to the long-range repulsive electrostatic interaction between the stabilized bubbles, and this contributes to foam stability. In the fifth part, the aim was to develop the drying procedure in order to producea dry porous CNF material using the wet foam as a precursor and to evaluate the dry foam properties. The wet foam was dried in an oven while placed on a liquid-filled porous ceramic frit to preserve and enhance the porous structure in the dried material and prevent the formation of larger cavities and disruptions. The cell structure has been studied by SEM microscopy and APVD (automatic pore volume distribution). The mechanical properties have been studied by a tensile tester (Instron 5566) and the liquid absorption ability with the aid of the APVD-equipment. By changing the charge density of the CNFs it is possible to prepare dry foams with different densities and the lowest density was found to be 6 kg m-3with a porosity of 99.6 %. The Young ́s modulus in compression was 50 MPa and the energy absorption was 2340kJ m-3 for foams with a density of 200 kg m-3. The liquid absorption of the foam with a density of 13 kg m-3 is 34 times its own weight. By chemically cross-linking the foam,it wasalso possible to empty the liquid-filled foams by compression and then to reabsorb the liquid to the same degree with maintained foam integrity. This new processing method also shows great promise for preparing low-density cellulose foams continuously and could be very suitable for industrial up-scaling. / <p>QC 20141103</p>

<p>In this thesis, porous graphitic carbon (PGC) has been used as packing material in packed capillary liquid chromatography. The unique chromatographic properties of PGC has been studied in some detail and applied to different analytical challenges using both electrospray ionization-mass spectrometry (ESI-MS) and ultra violet (UV) absorbance detection. </p><p>The crucial importance of disengaging the conductive PGC chromatographic separation media from the high voltage mass spectrometric interface has been shown. In the absence of a grounded point between the column and ESI emitter, a current through the column was present, and changed retention behaviors for 3-O-methyl-DOPA and tyrosine were observed. An alteration of the chromatographic properties was also seen when PGC was chemically oxidized with permanganate, possibly due to an oxidation of the few surface groups present on the PGC material. </p><p>The dynamic adsorption of the chiral selector lasalocid onto the PGC support resulted in a useful and stable chiral stationary phase. Extraordinary enantioselectivity was observed for 1-(1-naphthyl)ethylamine, and enantioseparation was also achieved for other amines, amino acids, acids and alcohols. </p><p>Finally, a new strategy for separation of small biologically active compounds in plasma and brain tissue has been developed. With PGC as stationary phase it was possible to utilize a mobile phase of high content of organic modifier, without the addition of ion-pairing agents, and still selectively separate the analytes. </p>

In this thesis, porous graphitic carbon (PGC) has been used as packing material in packed capillary liquid chromatography. The unique chromatographic properties of PGC has been studied in some detail and applied to different analytical challenges using both electrospray ionization-mass spectrometry (ESI-MS) and ultra violet (UV) absorbance detection. The crucial importance of disengaging the conductive PGC chromatographic separation media from the high voltage mass spectrometric interface has been shown. In the absence of a grounded point between the column and ESI emitter, a current through the column was present, and changed retention behaviors for 3-O-methyl-DOPA and tyrosine were observed. An alteration of the chromatographic properties was also seen when PGC was chemically oxidized with permanganate, possibly due to an oxidation of the few surface groups present on the PGC material. The dynamic adsorption of the chiral selector lasalocid onto the PGC support resulted in a useful and stable chiral stationary phase. Extraordinary enantioselectivity was observed for 1-(1-naphthyl)ethylamine, and enantioseparation was also achieved for other amines, amino acids, acids and alcohols. Finally, a new strategy for separation of small biologically active compounds in plasma and brain tissue has been developed. With PGC as stationary phase it was possible to utilize a mobile phase of high content of organic modifier, without the addition of ion-pairing agents, and still selectively separate the analytes.

This thesis explores the heat transfer characteristics of a packed bed thermal energy storage device through the development of a 3D model in COMSOL Multiphysics. The model is based on a laboratory-scale device consisting of an aluminum box filled with sand, which acts as the thermal storage medium. The medium is heated using two resistance heaters that are embedded into the sand. The heaters are raised to approximately 500°C during the experiment. Three thermocouples placed in the sand record the temperature during charging, thus generating a time-dependent temperature curve at three points. The model simulates this experimental system, and the resulting temperature distribution is compared to the experimental data to assess the model validity. To determine the temperature throughout the storage system at all times, the model solves the heat equation. The density and heat capacity of the sand are measured and added to the model. The model uses the effective medium technique to estimate the thermal conductivity of the sand. A secondary model is developed in Excel to calculate the effective thermal conductivity using twelve different correlations, and the results are compared. The Zehner-Bauer correlation with an added Damköhler radiation term predicted an effective thermal conductivity of 0.218 W/(m·K) at 25°C and 0.451 W/(m·K) at 500°C, with slightly exponential growth due to the influence of thermal radiation. When these values for conductivity are applied to the COMSOL model, there is strong agreement (average percent error &lt; 5%) with the experimental temperature distributions. A parametric study is performed, and shows that increasing grain size and emissivity could increase the thermal conductivity by making use of the exponential growth of thermal radiation. The model serves as a design and learning tool, and a starting point for improving the performance of the thermal energy storage system. / Detta examensarbete undersöker värmeöverföringsegenskaperna hos en termisk energilagringsenhet med packad bädd genom utveckling av en 3D-modell i COMSOL Multiphysics. Modellen är baserad på en enhet i laboratorieskala som består av en aluminiumlåda fylld med sand, som fungerar som det termiska lagringsmediet. Mediet värms upp med hjälp av två motståndsvärmare som är inbäddade i sanden. Värmeelementen höjs till ca 500°C under experimentet. Tre termoelement placerade i sanden registrerar temperaturen under laddningen och genererar på så sätt en tidsberoende temperaturkurva i tre punkter. Modellen simulerar detta experimentella system, och den resulterande temperaturfördelningen jämförs med experimentella data för att bedöma modellens giltighet. För att bestämma temperaturen i hela lagringssystemet vid alla tidpunkter löser modellen värmeekvationen. Sandens densitet och värmekapacitet mäts och läggs till i modellen. Modellen använder den effektiva mediumtekniken för att uppskatta sandens värmeledningsförmåga. En sekundär modell utvecklas i Excel för att beräkna den effektiva värmeledningsförmågan med hjälp av tolv olika korrelationer, och resultaten jämförs. Zehner-Bauer korrelationen med en tillagd Damköhler strålningsterm förutsade en effektiv värmeledningsförmåga på 0,218 W/(m·K) vid 25°C och 0,451 W/(m·K) vid 500°C, med en något exponentiell tillväxt på grund av påverkan från värmestrålning. När dessa värden för konduktivitet tillämpas på COMSOL-modellen finns det en stark överensstämmelse (genomsnittligt procentuellt fel &lt; 5%) med de experimentella temperaturfördelningarna. En parametrisk studie har utförts som visar att ökad kornstorlek ock emissivitet kan öka värmeledningsförmågan genom att utnyttja den exponentiella tillväxten av värmestrålning. Modellen fungerar som ett design- och inlärningsverktyg och som en utgångspunkt för att förbättra prestandan hos det termiska energilagringssystemet.