The number of hardened surfaces has increased as a result of urbanization, and thus also the amount of road stormwater. Road stormwater can transport pollutants that have been released on road areas to surrounding recipients. Two substances that are found in particularly high concentrations in road storm water are copper and zinc. At high concentrations of these substances, toxic effects occur which are particularly harmful to aquatic organisms. This report intends to investigate how well the filter material Polonite purifies road stormwater from copper and zinc. Polonite is a reactive filter material made of the sedimentary rock Opoka, which binds substances such as copper and zinc by adsorption. In this thesis, a laboratory experiment has been carried out where it has been investigated how well different amounts of Polonite adsorb copper and zinc during different time periods. The results show that the concentrations of copper and zinc generally decreased over time and with an increasing amount of Polonite. Furthermore, a simulation of how Polonite's purification capacity decreases over time has been created. The simulation showed that Polonite's ability to purify stormwater according to the guideline values ceases after 133 days for copper and 325 days for zinc. Data collected from a column experiment was then compared with the simulation. The comparison showed that the simulation for zinc was in good agreement with the data from the column experiment, while the data for copper were more different from the simulation.  Conclusions drawn are that Polonite can be a good solution for sustainable road stormwater management as it can purify zinc and copper in accordance with the recommended guideline values. The results also show that Polonite has a better ability to purify zinc than copper and that it can purify zinc for a longer period of time. Moreover, other aspects such as economics need to be investigated in future studies to establish with certainty that Polonite is a good solution for the purification of road stormwater in large-scale treatment plants. / Till följd av urbaniseringen ökar antalet hårdgjorda ytor, och därmed även mängden vägdagvatten. Vägdagvatten kan transportera föroreningar som uppkommit på vägområden till omgivande recipienter. Två ämnen som hittas i särskilt höga koncentrationer i vägdagvatten är koppar och zink.  Vid höga koncentrationer av dessa ämnen uppstår toxiska effekter som är särskilt skadliga för vattenlevande organismer. Denna rapport ämnar att undersöka hur väl filtermaterialet Polonite renar vägdagvatten från koppar och zink. Polonite är ett reaktivt filtermaterial som genom adsorption kan rena vägdagvatten. I detta arbete har en laboration utförts där det har undersökts hur väl olika mängder Polonite adsorberar koppar och zink under olika tidsperioder. Resultatet visar att halterna koppar och zink generellt minskar med tiden samt med ökande mängd Polonite. Vidare skapades en simulering av hur Polonites reningsförmåga minskar med tiden.  Slutsatser som dragits är att Polonite kan vara en god lösning för hållbar vägdagvattenhantering då det kan rena koppar och zink i enlighet med de rekommenderade riktvärdena. Resultatet visar även att Polonite har en bättre förmåga att rena zink än koppar samt att det kan rena zink under en längre tidsperiod. För att med säkerhet fastställa att Polonite är en bra lösning för rening av vägdagvatten i storskaliga reningsanläggningar behöver flera aspekter såsom ekonomi undersökas i framtida studier.

MOF-5 ist der Archetyp einer neuartigen Klasse hochporöser Materialien, den Metal Organic Frameworks, die unter anderem zur Anwendung als effektive Gasspeicher geeignet sind. Im Rahmen dieser Arbeit werden die seiner Bildung zugrunde liegenden Reaktionen untersucht. Aus den Erkenntnissen dieser Untersuchungen wurden zwei neue Syntheseverfahren entwickelt. Eines der Verfahren beruht auf der Phasenumwandlung von Zinkterephthalaten und ermöglichte die Laborsynthese von MOF-5 in 100 g-Mengen. Ein zweites Verfahren bedient sich des Strukturaufbaus mit Hilfe vorgefertigter anorganischer Cluster, wodurch erstmals die Synthese von MOF-5-Homologen anderer Metalle als Zink gelang.

<p>Dagvatten från vägar innehåller ofta tungmetaller. De vanligaste metallerna i vägdagvatten är bly, koppar, kadmium, nickel och zink. Dessa föroreningar utgör en belastning i recipienter som tar emot dagvattnet. I denna rapport har bly, koppar och zink reducerats från vägdagvatten genom filtrering i kolonner med amorf, granulerad masugnsslagg och sand. Masugnsslagg, som är en biprodukt från framställningen av järn, är en alkalisk produkt med goda sorptionsegenskaper vilket gör den lämplig att använda som filtermaterial för vatten förorenade med metaller. Sanden användes i studien som referensmaterial. Masugnsslaggen som användes i denna studie är hyttsand från Merox, Oxelösund. Reningshalten för hyttsanden i denna studie uppgick till 79 % för bly, 82 % för koppar samt 92 % för zink. Hyttsandens reducerande förmåga har även undersökts i batchförsök.</p> / <p>Stormwater from roads often contain heavy metals. The most common metals in storm water from roads are lead, copper, cadmium, nickel, and zinc. These pollutants constitute a stress for organisms in recipients that receive the stormwater. In this report lead, copper and zinc have been reduced from road storm water through filtration in columns with granulated iron slag and sand. Iron slag is a by-product from the iron making process, with a high sorption capacity, which makes it suitable as a filter material for water polluted with metals. The sand in this study has been used as reference material. The reducing capacity in the stormwater for the iron slag used in this study, “hyttsand”, was 79 % for lead, 82 % for copper and 92 % for zinc. The reducing capacity of the iron slag was also investigated in batch studies.</p>

This thesis deals with the preparation of chemically and/or enzymatically modified cellulose. This modification can be either irreversible or reversible. Irreversible modification is used to prepare cellulose derivatives as end products, whereas reversible modification is used to enhance solubility in the preparation of regenerated cellulose. The irreversible modification studied here was the preparation of carboxymethyl cellulose (CMC) using extended mercerization of a spruce dissolving pulp. More specifically the parameters studied were the effect of mercerization at different proportions of cellulose I and II in the dissolving pulp, the concentration of alkali, the temperature and the reaction time. The parameters evaluated were the degree of substitution, the filterability and the amount of gel obtained when the resulting CMC was dissolved in water. Molecular structures of CMC and its gel fractions were analysed by using NIR FT Raman spectroscopy. It was found that the alkali concentration in the mercerization stage had an extensive influence on the subsequent etherification reaction. FT Raman spectra of CMC samples and their gel fractions prepared with low NaOH concentrations (9%) in the mercerization stage indicated an incomplete transformation of cellulose to Na-cellulose before carboxymethylation to CMC. Low average DS values of the CMC, i.e. between 0.42 and 0.50 were obtained. Such CMC dissolved in water resulted in very thick and semi solid gum-like gels, probably due to an uneven distribution of substituents along the cellulose backbone. FT Raman spectra of CMC samples and their gel fractions mercerized at higher alkaline concentration, i.e. 18.25 and 27.5% in the mercerization stage, indicated on the other hand a complete transformation of cellulose to Na-cellulose before carboxymethylation to CMC. Higher average DS values of the CMC, i.e. between 0.88 and 1.05 were therefore obtained. When dissolved in water such CMC caused gel formation especially when prepared from dissolving pulp with a high fraction of cellulose II. The reversible modification studied was the dissolution of cellulose in NaOH/ZnO. Here the effect of enzyme pretreatment was investigated by using two mono-component enzymes; namely xylanase and endoglucanase, used in consecutive stages. It was found that although the crystallinity and the specific surface area of the dissolving pulp sustained minimal change during the enzymatic treatment; the solubility of pulp increased in a NaOH/ZnO solution from 29% for untreated pulp up to 81% for enzymatic pretreated pulp. / Baksidetext Cellulose can be chemically and/or enzymatically modified. Irreversible modification is used to prepare cellulose derivatives as end products, reversible modification to enhance solubility in the preparation of regenerated cellulose. The irreversible modification studied here was the preparation of carboxymethyl cellulose (CMC) using extended mercerization of a spruce dissolving pulp. More specifically the parameters studied were the effect of mercerization at different proportions of cellulose I and II in the dissolving pulp, the concentration of alkali, the temperature and the reaction time. It was found that the alkali concentration in the mercerization stage had an extensive influence on the subsequent etherification reaction. The content of cellulose II had little effect on degree of substitution (DS) at low NaOH concentration, but tended to decrease DS at higher NaOH concentration in both cases compared with cellulose I. It was also found that the content of cellulose II correlates with the gel formation obtained when the CMC is dissolved in water. The reversible modification studied was the dissolution of cellulose in NaOH/ZnO. Here the effect of enzyme pretreatment was investigated by using two mono-component enzymes; namely xylanase and endoglucanase, used in consecutive stages. It was found that the solubility of pulp increased in a NaOH/ZnO solution from 29% for untreated pulp up to 81% for enzymatic pretreated pulp.

Solid state lighting is a new environmentally friendly light source. So far, light emitting diodes (LEDs) and organic LEDs (OLEDs) have been presented as candidates with potentially high efficiency. Recent advances of OLEDs in device architecture, light-out coupling, and materials have ensured high efficiency, exceeding that of incandescent light bulbs. In contrast to conventional point source LEDs, OLEDs distribute light throughout the surface area and are not restricted by their size. Additionally, OLEDs are expected to reach sufficient stability in the near future. The remaining challenge for OLEDs is their cost. New OLED technologies provide cost effective manufacturing methods which could be presented for transparent electrode materials because indium tin oxide (ITO), a widely used material as a transparent electrode for OLEDs, is less than optimal due to its high element price. In this work, alternative transparent electrodes for OLEDs as a replacement of ITO were studied. First, Al doped ZnO (ZnO:Al) which is composed of abundant materials was investigated with DC magnetron sputtering under a wide range of experimental conditions. The optimised ZnO:Al received comparable performance with conventional ITO films, low sheet resistance of 22.8 Ω/sq as well as a high transparency of 93.1 % (average value in the visible range). Various type of p-i-n OLEDs were employed on the structured ZnO:Al using photolithography. Green OLEDs with double emission layers have been archived stable efficiencies even at higher luminance. Also, OLEDs using two fluorescent colour system on ZnO:Al anode showed a purely white emission. It has been found that the OLEDs on ZnO:Al anode has comparable or better device efficiencies and operational lifetime compared to OLEDs on conventional ITO anode. As another alternative electrode, the conductive polymer Baytron®PH510 (PEDOT:PSS) was investigated. Due to a relatively high sheet resistance of PEDOT:PSS, metal grid was designed for large size OLEDs. White OLEDs on PEDOT anode with a size of 5 × 5 cm2 have achieved more than 10 lm/W of power efficiency using a scattering foil. Furthermore, up-scaled devices on 10 × 10 cm2 were also demonstrated. These results showed ZnO:Al and PEDOT are suitable for OLEDs as anode and have high potential as alternative transparent electrode materials.

Dagvatten från vägar innehåller ofta tungmetaller. De vanligaste metallerna i vägdagvatten är bly, koppar, kadmium, nickel och zink. Dessa föroreningar utgör en belastning i recipienter som tar emot dagvattnet. I denna rapport har bly, koppar och zink reducerats från vägdagvatten genom filtrering i kolonner med amorf, granulerad masugnsslagg och sand. Masugnsslagg, som är en biprodukt från framställningen av järn, är en alkalisk produkt med goda sorptionsegenskaper vilket gör den lämplig att använda som filtermaterial för vatten förorenade med metaller. Sanden användes i studien som referensmaterial. Masugnsslaggen som användes i denna studie är hyttsand från Merox, Oxelösund. Reningshalten för hyttsanden i denna studie uppgick till 79 % för bly, 82 % för koppar samt 92 % för zink. Hyttsandens reducerande förmåga har även undersökts i batchförsök. / Stormwater from roads often contain heavy metals. The most common metals in storm water from roads are lead, copper, cadmium, nickel, and zinc. These pollutants constitute a stress for organisms in recipients that receive the stormwater. In this report lead, copper and zinc have been reduced from road storm water through filtration in columns with granulated iron slag and sand. Iron slag is a by-product from the iron making process, with a high sorption capacity, which makes it suitable as a filter material for water polluted with metals. The sand in this study has been used as reference material. The reducing capacity in the stormwater for the iron slag used in this study, “hyttsand”, was 79 % for lead, 82 % for copper and 92 % for zinc. The reducing capacity of the iron slag was also investigated in batch studies.

No description available.

No description available.

With the advancement and accessibility of local probing techniques that can operate at the submicron scale it has become possible to analyse the local corrosion properties of industrially important metallic materials and relate these properties to microstructure characteristics of the same materials. In this doctoral study the focus has been on copper-zinc samples, both as industrial brass alloys and as micro-patterned copper-zinc samples. They have been exposed to dilute chloride solutions and to an atmosphere that mimics indoor conditions that cause corrosion. The main goal has been to investigate micro-galvanic effects caused by surface heterogeneities in the copper-zinc samples, and the corrosion inhibition ability of a self-assembled octadecanethiol (ODT, CH3(CH2)17SH) monolayer when applied to these heterogeneous samples. The local chemistry, local electrochemistry, and local surface chemistry in the presence of the copper-zinc galvanic couplings have been elucidated, and their importance has been investigated for corrosion initiation, propagation, termination, and inhibition. A broad spectrum of local probe techniques has been utilised. They include optical microscopy (ex situ and in situ), electrochemical techniques, scanning electron microscopy with energy dispersive spectroscopy, atomic force microscopy, scanning Kelvin probe force microscopy and confocal Raman spectroscopy. In addition, infrared reflection absorption spectroscopy (in situ) and vibrational sum frequency spectroscopy have been employed to analyse the formation of corrosion products and monitor the corrosion kinetics.    A characteristic selective zinc dissolution process was triggered in non-metallic inclusions when a brass alloy was exposed to 1 mM NaCl. Disc-like corrosion areas spread radially outwards from the inclusions, the shape and termination of which was attributed to accessibility to chloride ions. An ODT-layer deposited on brass retarded access to chloride ions at the brass surface and slowed down the radial corrosion process. Instead a delayed formation of filiform-like corrosion was observed.    Upon exposure of the copper-zinc patterned sample to humidified air containing formic acid, micro-galvanic effects were induced by the copper patches on zinc that accelerated the zinc dissolution in the thin aqueous adlayer with concomitant precipitation of zinc formate. The micro-galvanic effects not only resulted in accelerated corrosion rates for zinc, but also in broadening of shapes and atomic structures for the corrosion products formed. Crystalline zinc oxide and zinc formate were observed on the copper-zinc patterned samples, whereas amorphous zinc oxide and zinc formate were formed on the bare zinc surface. Micro-galvanic effects occurred in the two-phase Cu40Zn (Cu with 40 wt% Zn) brass alloy as well, induced by more zinc-rich beta-phase grains surrounded by an alpha matrix with lower zinc-content.    The application of a self-assembled monolayer of ODT for corrosion inhibition of pure zinc and the patterned copper-zinc samples was also explored. In situ infrared reflection absorption spectroscopy analyses showed that ODT initially reduced the rate of zinc formate formation on pure zinc and on the copper-zinc micro-patterned sample. However, the inhibition efficiency was slightly reduced with exposure time due to local removal of ODT on pure zinc and on the micro-patterned samples. This caused micro-galvanic effects that resulted in increased rates of zinc formate formation on the ODT-covered samples – even higher than on the uncovered samples. When applied to the single-phase Cu20Zn alloy, ODT resulted in a corrosion inhibition that was comparable to that of pure copper, a metal for which ODT has shown very good corrosion inhibition. On double-phase Cu40Zn local galvanic effects resulted in less efficient corrosion inhibition and more abundant corrosion products than on Cu20Zn. Based on vibrational sum frequency spectroscopy, the ODT-layer retained its well-ordered molecular structure throughout the exposure to both Cu20Zn and Cu40Zn.    In all, the inhibiting action of the ODT-layer was attributed to the transport hindrance of corrosion promoters (O2, H2O, and HCOOH) to the brass surface. This result suggests that ODT can function as a temporary corrosion inhibitor for brass exposed to benign indoor environments. / Med utvecklingen av och tillgången till lokala analysmetoder som kan ge information med en lateral upplösning på mindre än en mikrometer har det blivit möjligt att analysera lokala korrosionsegenskaper hos industriellt viktiga metalliska material och relatera dessa egenskaper till mikrostrukturen hos samma material. I doktorsavhandlingen har denna möjlighet utnyttjats för koppar-zinkprover, dels som industriella mässingslegeringar dels som mikro-mönstrade koppar-zinkprover, som exponerats för utspädda kloridlösningar samt för en atmosfär som kan efterlikna den atmosfäriska korrosionen inomhus. Det huvudsakliga målet har varit att undersöka dels mikro-galvaniska korrosionseffekter som orsakas av heterogeniteter på koppar-zinkytorna dels korrosionsförmågan hos självorganiserande monolager av oktadekantiol (ODT, CH3(CH2)17SH) vid adsorption på dessa heterogena ytor. På så vis har den lokala kemin, ytkemin och elektrokemin kunnat klarläggas i närvaro av galvaniska effekter, och dess betydelse har undersökts för korrosionsprocessens initiering, propagering, terminering och inhibering. Ett brett spektrum av lokala analysmetoder har utnyttjats. De innefattar ljusoptisk mikroskopi (ex situ och in situ), elektrokemiska metoder, svepelektronmikroskopi med energidispersiv röntgen-spektroskopi, atomkraftsmikroskopi för mikro-kartering och Voltapotentialmätningar samt konfokal Raman-spektroskopi. Dessutom har infrarödreflektions absorptionsspektroskopi (in situ) och vibrationssummafrekvens spektroskopi (engelska: vibrational sum frequency generation) använts.    När en mässingslegering exponerades för 1 mM NaCl observerades en selektiv utlösning av zink med karakteristiskt utseende som växte radiellt från icke-metalliska inneslutningar för att bilda cirkulärt formade korrosionsområden. Formen och termineringen av denna korrosionsprocess bestäms av tillgången på kloridjoner. När ett monolager av ODT adsorberades på mässingslegeringen hämmades tillgången av kloridjoner på mässingsytan och den radiella korrosionsprocessen stannade upp. Istället iakttogs en fördröjd bildning av s.k. filiform korrosion.    Vid exponering av mikro-mönstrade koppar-zinkprover för befuktad luft med låga tillsatser av myrsyra inducerades mikro-galvaniska effekter i gränsen mellan koppar och zink som accelererade utlösningen av zink i den adsorberade fuktfilmen på provet, under samtidig utfällning av zinkformat. De mikro-galvaniska effekterna resulterade inte bara i förhöjda korrosionshastigheter jämfört med de på ren zink, utan även i andra faser hos bildade korrosionsprodukter. På de mikro-mönstrade koppar-zinkproverna bildades kristallint zinkoxid och zinkformat, under det att amorft zinkoxid och zinkhydroxyformat bildades på ren zink. Mikrogalvaniska effekter observerades även i den tvåfasiga mässingslegeringen Cu40Zn (Cu med 40 vikt-% Zn) orsakade av kontakten mellan den mer zinkrika beta-fasen och den omgivande alfa-fasen med lägre zinkhalt.    Appliceringen av ett självorganiserat monolager av ODT för korrosionsinhibering av ren zink och koppar-zinkprover har också undersöks. In situ infrarödreflektions absorptionsspektroskopi visade att adsorberat ODT initialt hämmade bildningen av zinkformat på ren zink och på de mikro-mönstrade koppar-zinkproverna. Med tiden minskade ODTs korrosionsinhiberings-förmåga på grund av att ODTs vidhäftning lokalt försvann. De mikro-galvaniska effekter som därigenom uppstod resulterade i bildandet av zinkformat som med tiden blev snabbare på de ODT-belagda proverna än på motsvarande prover utan ODT. När ODT applicerades på den enfasiga mässingslegeringen Cu20Zn resulterade detta i en korrosionsinhibering som var jämförbar med den på ren koppar, en metall på vilken ODT tidigare visat mycket bra korrosionsskydd. På den tvåfasiga mässingslegeringen Cu40Zn ledde lokala galvaniska effekter till en mindre effektiv korrosions-inhibering och en rikligare mängd korrosionsprodukter än på Cu20Zn. Baserat på vibrationssummafrekvens spektroskopi behöll ODT-lagret dess välordnade struktur under hela exponeringen på både Cu20Zn och Cu40Zn.    ODTs korrosionsinhibering tillskrivs främst transport-hämningen av korrosionsstimulatorer (O2, H2O och HCOOH) till mässingsytan och antyder att ODT kan fungera som en temporär korrosionsinhibitor för mässing i milda inomhusmiljöer. / <p>QC 20140915</p>

Dans cette thèse, nous étudions la géométrie analytique p-adique et la cohomologie l-adique de certains espaces de Rapoport-Zink, en utilisant la théorie des filtrations de Harder-Narasimhan des schémas en groupes finis et plats élaborée par Fargues.Cette thèse se compose de trois parties. La première partie traite de certains espaces de Rapoport-Zink non-basiques, qui satisfont à la condition que leur polygone de Newton et polygone de Hodge ont un point de contact non-trivial, qui est un point de rupture pour le polygone de Newton. Sous cette hypothèse, nous prouvons que ces espaces de Rapoport-Zink peuvent être décomposés en une somme directe d'espaces de modules des types de Rapoport-Zink associés à certains sous-groupes paraboliques appropriés, donc leurs cohomologie l-adique sont des induites paraboliques et en particulier ne contiennent pas de représentations supercuspidales. Nous prouvons ces faits en démontrant d'abord un théorème sur la filtration de Hodge-Newton pour les groupes p-divisibles avec des structures additionelles sur des anneaux de valuation complets de rang un et de caractéristique mixte (0,p).Dans la deuxième partie, nous considérons les espaces de Rapoport-Zink basiques de signature (1,n-1) pour les groupes unitaires associés à l'extension quadratique non ramifiée de Qp. On étudie l'action de Hecke sur ces espaces en détails. En utilisant la théorie des filtrations de Harder-Narasimhan des schémas en groupes finis et plats, et la stratification de Bruhat-Tits de la fibre spéciale réduite Mred étudié par Vollaard-Wedhorn, on trouve un certain domaine analytique compact DK telle que ses itérés dans le groupe G(Qp)×Jb(Qp) forme un recouvrement localement fini de tout l'espace MK. Nous appelons un tel phénomène une décomposition cellulaire localement finie.Dans la troisième partie, nous démontrons une formule de Lefschetz pour ces espaces pour l'action des éléments semi-simples réguliers elliptiques, en tenant compte de l'action de ces éléments sur les cellules et en appliquant le théorème principal de Mieda. De la même manière, nous pouvons aussi reprouver la formule de Lefschetz pour les espaces de Lubin-Tate précédemment obtenue par Strauch et Mieda. Cette formule de Lefschetz devrait caractériser la réalisation de correspondances de Jacquet-Langlands locales pour les groupes unitaires dans la cohomologie l-adique de ces espaces de Rapoport-Zink, dès que certains problèmes correspondants de théorie des représentations auront été résolus.