Dissertations / Theses on the topic 'Colloid and Surface Chemistry'

Paper and board are hydrophobized (sized) to control the spreading and absorption of waterbased inks and retard the absorption and edge penetration of liquid packaging by aqueous liquids. Alkenyl ketene dimers (AKD) and alkenyl succinic anhydride (ASA) are synthetic sizing agents that are generally used under neutral or slightly alkaline papermaking conditions. The overall objective of this thesis is to improve understanding of the internal sizing of paper and board by AKD and ASA by establishing a link between the sizing mechanism on one hand, and properties of sized papers, such as surface chemistry, wettability and friction, on the other. Fundamental research has been conducted in parallel with more applied research on laboratory and pilot papers. Significant effort has been expended to study the spreading behavior of AKD. The main instrument to characterize the surface chemical composition of AKD and ASA sized papers was X-ray photoelectron spectroscopy (XPS). By combination with time-of-flight secondary ion mass spectrometry (ToF-SIMS) we have been able to determine the lateral distribution and the chemical state of the sizing agent at the paper surface. Combined with contact angle measurements using liquids with different surface tensions, and other methods to analyze the amounts of size in paper, this has enabled us to obtain a deeper knowledge of the sizing mechanisms of AKD and ASA. The results indicate a definitive relationship between the redistribution of AKD at the surface of pilot papers and the drying profile used during papermaking. However, the spreading was not complete, as also seen on a model surface. Further spreading of AKD was shown to occur via surface diffusion in the form of an autophobic monolayer precursor. The spreading rate increased linearly with temperature and showed an inverse proportionality with respect to the melting point of the AKD. This monolayer spreading is relatively slow the diffusion coefficient being of the order 10-11 m2/s. AKD spreading was not hindered by hydrolyzed AKD (ketone) that spread as well. Moreover, AKD spread on the surface of crystalline calcium carbonate. In laboratory papers, the extractives present on CTMP fiber surfaces appeared to have enhanced the spreading of AKD when the fibers were in water. In spite of a slightly lower retention, ASA covered the surface of unfilled and PCC-filled pilot papers to a significantly higher extent than AKD. The ASA sized papers, however demonstrated slightly lower resistance to water. This was attributed to formation of hydrolyzed ASA products. The results obtained confirm the proposed sizing mechanism for ASA, where the hydrolyzed ASA plays a key role. The sizing level of these papers stored wrapped in aluminium foil at 23 °C and 5O %RH was nearly unchanged over prolonged storage time. In contrast, the papers exposed to ambient conditions suffered from sizing loss, most likely due to hydrolysis and migration. The reduction of the sizing degree was higher for the AKD than ASA sized unfilled papers and the catalytic effect of PCC contributed to the hydrolysis of AKD in PCC-filled papers. As expected, the use of sizing agent reduced the surface energy of paper. The higher the sizing degree of paper the lower the surface energy, and thus the higher the resistance to wetting. This was particularly seen in the contact angles with ethylene glycol having a lower surface tension than water. AKD significantly decreased the friction between unfilled papers, whereas ASA had no impact. This difference was attributed to surface chemical composition. Friction reduction for the AKD sized papers started at the AKD coverage normally found in paper produced for low water absorption. As expected, PCC filler increased paper-to-paper friction.
Papper och kartong hydrofoberas (limmas) för att kontrollera spridning och absorption avvattenbaserade tryckfärger och hindra kantinträngning av vattenbaserade vätskor ivätskekartong. Alkylketendimer (AKD) och alkylbärnstensyra anhydrid (ASA) är syntetiskahydrofoberingsmedel som allmänt används under neutrala eller något alkaliska förhållandenvid papperstillverkning.Arbetets övergripande målsättning var att förbättra förståelse för mäldhydrofobering avpapper och kartong med AKD och ASA genom att upprätta ett samband mellanhydrofoberingsmekanism på ena sida och ytkemi hos hydrofoberat papper och dessvätningsförmåga och friktion på den andra sidan. Grundläggande studier parallellt med mertillämpade undersökningar på laboratorie- och pilotpapper har utförts. En betydande strävanhar använts för att studera spridning av AKD. Huvudinstrumentet för att karakterisera kemisksammansättning av ytan av pilotpapper hydrofoberade med AKD och ASA var röntgenfotoelektron spektroskopi (XPS). Genom att kombinera det med sekundär jonmasspektrometri (ToF-SIMS) har lateral fördelning och kemiskt tillstånd av AKD och ASAvid en yta av papper kunnat bestämmas. Kombinerat med mätningar av kontaktvinkel medvätskor med olika ytspänning och andra metoder för att analysera halten avhydrofoberinsgmedel i papper har gjort det möjligt att erhålla djupare kunskap omhydrofoberingsmekanismer av AKD och ASA.Resultaten indikerar en klar koppling mellan omfördelning av AKD på ytan av pilotpapperoch torkningsprofil vid papperstillverkning. Emellertid, spridningen var inte fullständig, vilketvar fallet även på modellytor. Fortsatt spridning av AKD visades ske som ytdiffusion i formav ett autofobiskt monoskikt (precursor film). Spridningshastigheten ökade linjärt medtemperatur och visade omvänd proportionalitet med avseende på AKD:s smältpunkt. Dennamonoskiktspridning är relativt långsam, diffusionshastighet är i storleksordningen 10-11 m2/s.Hydrolyserat AKD (keton) hindrade inte AKD:s spridning utan spred även den. Dessutomspred AKD på ytan av kristallina kalciumkarbonat. I laboratoriepapper är extraktivämnennärvarande på ytor av CTMP fiber och tycktes ha förbättrat AKD:s spridning när fibrerna varunder vatten.ivTrots något lägre retention täckte ASA ytan av icke-fyllda och PCC-fyllda papper tillsignifikant högre grad än AKD. ASA-papperen visade dock något lägre motstånd mot vatten.Detta var hänvisat till bildning av hydrolyserade ASA-produkter. De uppnådda resultatenbekräftar den föreslagna hydrofoberingsmekanismen för ASA, där hydrolyserat ASA spelaren avgörande roll. Hydrofoberingsgraden av papper lagrade inlindade i aluminiumfolie vid23 °C och 50 RH var nästan oändrad över den förlängda lagringstiden. Som motsatsgenomgick papperen som exponerats mot omgivande atmosfärsförhållanden genomgick enminskning av hydrofoberingsgraden, troligen på grund av hydrolys och migrering. Minskningav hydrofoberingsgraden var större för icke-fyllda papper av AKD än av ASA. PCC:skatalytiska effekt bidrog till hydrolys av AKD i PCC-fyllda papper.Som förväntat reducerade användning av hydrofoberingsmedel reducerade ytenergin avpapper. Ju högre hydrofoberingsgrad desto lägre var ytenergin och därmed desto högremotstånd mot vätning. Detta sågs särskilt i kontaktvinklar med etylenglykol som har lägreytspänning än vatten.AKD minskade signifikant friktionen mellan icke-fyllda papper, medan ASA inte hadeinverkan. Denna skillnad hänfördes till skillnad i ytsammansättning. Minskning av friktion förAKD-hydrofoberade papperen påbörjades vid en sådan yttäckning av AKD som är normaltför papper tillverkat för låg vattenabsorption. Som förväntat ökade PCC-fyllmedel friktionenmellan papperen.
QC 20100817

The focus in this thesis has been to gain a fundamental understanding of how different type of salts affect preadsorbed polyelectrolytes, both natural and synthetic. The knowledge from the fundamental work is then applied on a commercial system to investigate if the efficiency can be enhanced. We built thin films using the synthetic polyelctrolytes by using layer-by layer (LbL) deposition. The formed film is commonly known as a polyelectrolyte multilayer. The LbL method allows the incorporation of proteins, polymers, polyelectrolytes with different functions and so on within the film, thus achieving multilayers with different functions. The major measuring technique used within this thesis is the quartz crystal microbalance with dissipation (QCM-D), which measures mass adsorbed on a surface including the trapped solvent and the viscoelastic properties of an adsorbed film. The QCM-D measurements were complemented with an optical technique, dual polarization interferometry (DPI), which measures the change in refractive index and thickness. From these parameters the dry mass and relative water content of the film can be calculated. The Atomic Force Microscopy (AFM) further gave information about forces acting between preadsorbed films. We investigated the effect of salt on synthetic polyelectrolyte poly(allylamine hydrochloride)/poly(sodium 4-styrenesulfonate) built with the LbL technique, thus forming polyelectrolyte multilayers. We concluded that the multilayer build-up was linear and that the internal structure of the multilayer is of a compact and rigid nature. However, the type of rinsing protocol (termination of adsorption by: salt, water and salt first followed by water) has a significant effect on the outer layer of the formed multilayer. Interestingly, the structural changes only applied when poly(allylamine hydrochloride) was at the outermost layer and the most significant when water was used. We suggest that it is only the top layer that swells due to the removal of counterions resulting in increased intrachain repulsion. We further performed two-layer model calculations with the Voight model to confirm the QCM-D results as well as a novel two layer model simulation for the DPI data in order to resolve the thickness. The model calculations were in good agreement with each other thus we concluded that only the outer layer swells for this particular multilayer system. In a related experiment we studied the adsorption of bovine submaxillary mucin (BSM), which has an important mucousal function, to different thiol modified gold surfaces as well as the effect of electrolytes (NaCl, CaCl2, LaCl3) on preadsorbed mucin to a hydrophobic thiol-modified Au surface. The salt induced an expansion at low concentrations; higher concentrations resulted in a compaction. Increasing the valence of the counter ion resultedin a compaction at low concentrations. The structural change of preadsorbed BSM was reversible for NaCl, partially reversible for CaCl2 and irreversible for LaCl3. Interestingly, the swelling of BSM could not be fully understood by using the QCM-D and thus AFM force curves of the same system were taken and the results showed that NaCl does decrease the tail length due to the effective screening of charged sites within the BSM molecule. Increasing the valence resulted in a notable compaction already at very low concentrations suggesting that the ions bind to the anionic sites on BSM. In the last work we attempted to combine the gained knowledge from the previous studies by using the LbL-buildup on an actual commercial health care application. The above-mentioned mutlilayer were used to coat polystyrene wells in order to increase the binding of immunoglobulin (IgG). The main goal was to increase the sensitivity of the conventional enzymelinked immunosorbent spot assay (ELISpot) and subsequently the modified polystyrene wells were used with the ELISpot test with human peripheral blood mononuclear cells (PBMC) to measure the cytokine response. We suggested that the main driving force for adsorption for IgG on a PAH terminated multilayer is electrostatic attraction, whereas on PSS terminated multilayer the driving force is hydrophobic. Further, we suggested that IgG  does not overcharge the surface and the linearity of the multilayer build-up is not altered when IgG is incorporated within the multilayer structure. We concluded that the cytokine response (spots) on the built multilayers regardless thickness or adsorbed IgG is significantly less than the regular polyvinyldiene fluoride (PVDF) backed ELISpot wells. We suggested that due to the compact and rigid nature of the PAH/PSS multilayer structure it is unable to form the kind of three-dimensional antibody-binding support found in the PVDF membrane. PSS terminated PAH/PSS multilayer did not induce any cytokine response whereas PAH terminated did, which suggests that PSS totally covers the surface from the cells point of view.
QC20100705

Unspecific interactions, at the interface between a synthetic material and an aqueous biological environment, leading to irreversible protein adsorption can cause to undesired consequences. These include fouling of a boat hull or a triggered immune response. Thus, stealthy materials are a topic that has generated a great deal of interest in the scientific community. This work deals with the design of networks, nanoparticles, and surfaces containing poly(ethylene glycol) (PEG), known for its resistance to protein adsorption and non-toxic nature. Initially, PEG-based networks, hydrogels, were synthesized using photoinduced thiol-ene chemistry in order to afford coatings targeted for marine antifouling applications. By varying the length of the PEG chain, curing chemistry, cross-linker as well as hydrolytical stability, a library of hydrogel coatings was produced. The coatings were subsequently characterized with respect to curing efficiency, thermal and mechanical properties, and aqueous stability. Furthermore, the antifouling properties of coatings were evaluated using in vitro tests with proteins, marine bacteria, and diatoms. As a final test the coatings were evaluated in a four month field test. It was found that coatings comprising longer PEG chains displayed enhanced antifouling performance, compared to shorter PEGs. In addition, the choice of cross-linker, curing chemistry, and hydrolytical stability also affected the properties to a great extent. This thesis further deals with the design of amphiphilic linear dendritic hybrids, with PEG as the hydrophilic block. Using non-toxic 2,2-bis(methylol) propionic acid (bis-MPA) based dendrons, bearing click functional cores (alkyne or allyl) and peripheral hydroxyl groups, as macrointitiators for ring-opening polymerization of ε-caprolactone, a library of star branched materials was afforded. As a final step, click functional (azide or thiol) PEGs were attached using copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) or thiol-ene click chemistry. The size of the dendrons was varied from generation 0-4, along with variation of both poly(ε-caprolactone) (PCL) length and PEG length. The materials were designed in order to allow a study of the impact of the dendron generation. Finally, the hybrid materials were used for the preparation of micelles, as well as for the formation of honeycomb membranes. The micelles critical micelle concentration, size and drug loading capacity were shown to be highly dependent on the generation of the dendron. The generation of the dendron also had a profound effect on the ability of the hybrid materials to form ordered honeycomb membranes, and hybrid materials of the 3rd generation yielded the most highly ordered membranes.
Ickespecifika interaktioner vid gränsytan, mellan ett syntetiskt material och en vattenbaserad biologisk miljö, kan leda till irreversibel adsorption av proteiner. Detta kan i sin tur leda till oönskade följdeffekter, såsom beväxning på båtskrov eller trigga en immunologisk reaktion. För att motverka dessa effekter har forskare utvecklat så kallade smygmaterial. Denna avhandling behandlar design av nätverk, nanopartiklar och ytor innehållande poly(etylenglykol) (PEG), som är känt för sina smygegenskaper och för att vara icke-toxiskt. Initialt behandlar avhandlingen PEG-baserade nätverk, hydrogeler, syntetiserade med fotoinitierad tiol-enekemi, för användning som beväxningsavvisande beläggningar för marina applikationer. Genom att variera olika parametrar, såsom längden på PEG-kedjan, härdningskemin, tvärbindaren samt den hydrolytiska stabiliteten, byggdes ett bibliotek av hydrogelbeläggningar upp. Hydrogelbeläggningarna karaktäriserades sedan med avseende på härdningseffektivitet, termiska och mekaniska egenskaper, samt hydrolytisk stabilitet. Vidare studerades beläggningarnas avvisande förmåga mot proteiner, bakterier samt kiselalger. Slutligen studerades ytbeläggningarna i ett fyra månader långt fälttest. Av testerna framgick att längre PEG-kedjor gav beläggningar med bättre avvisande förmåga. Dessutom framgick att valet av tvärbindare, härdningskemi samt hydrolytisk stabilitet var av betydelse för beläggningarnas effektivitet. Denna avhandling behandlar vidare design av amfifila linjära dendritiska hybridmaterial, med PEG som den hydrofila delen. Genom att använda icke-toxiska 2,2-bis(metylol)propionsyrabaserade dendroner, med en klickfunktionalitet i kärnan (alkyne eller allyl) och perifera hydroxylgrupper, som makroinitiatorer för ringöppningspolymerisation av ε-kaprolakton byggdes ett bibliotek av material upp. För att göra materialen amfifila, kopplades klickfunktionella PEG-kedjor (azid eller tiol) till kärnan med koppar(I)-katalyserad azid-alkyn cykloadditionskemi alternativt tiol-enekemi. Storleken på dendronerna varierades från generation 0-4, dessutom varierades längden på både poly(ε-kaprolakton)- och PEG-kedjorna. Materialen designades så att inverkan av dendrongenerationen kunde studeras. Slutligen användes dessa hybridmaterial för att framställa miceller samt isoporösa filmer. Micellernas kritiska micellbildningskoncentration, storlek samt förmåga att laddas med läkemedel visade sig vara mycket beroende av dendrongenerationen. Dendrongenerationen visade sig vidare även ha stor inverkan i hybridmaterialens förmåga att självorganisera sig till en isoporös struktur och material av tredje generationen gav de mest välordnade filmerna.
QC 20101125

The environmental stability of a metal / polymer interface is essential for the durability and mechanical stability of constructions in several important areas such as the automotive, offshore, building and aerospace industries. The protective capability of a polymer film is strongly connected to its barrier properties, but the transport of water and corrosive constituents through the polymer and the subsequent processes at the metal surface are complicated to analyse in detail. The surface to be analysed is confined between two media that are impermeable to most probing particles used in conventional analytical techniques. Several methods exist to describe separate parts of the system, but few techniques work atambient pressure and have the capacity to conduct real-time analysis at relevant exposure conditions. In this work, attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) in the Kretschmann geometry was successfully employed for systematic studies of metal / polymer interfaces. This technique requires the use of thin metal films deposited on an internal reflection element (IRE). Most studies were performed on aluminium, which is an important structural light-weight material, but also zinc was analysed, being frequently used for corrosion protection of steel. Upon exposure to water and electrolytes, the ATR-FTIR Kretschmann technique was found capable to monitor and to separate early deterioration related processes at the aluminium / polymer interface, including water sorption and transport of ionic species through the polymer film. Other main processes identified were the formation of corrosion products and swelling of the surface-near polymer network. To perform more comprehensive interpretations, a spectro-electrochemical method was further developed for in situ studies of the hidden metal / polymer interfaces. The ATR-FTIR Kretschmann technique was here combined with the complementary acting technique, Electrical Impedance Spectroscopy (EIS). The integrated set-up was able to provide complementary information, with ATR-FTIR Kretschmann being sensitive to the surface-near region and EIS to the whole system. For instance, metal oxidation and delamination processes can be difficult to distinguish by EIS, while on the other hand oxidation and hydration reactions on aluminiumcan be confirmed as IR bands at distinct positions. Delamination and swelling of a polymer both result in negative bands in an IR spectrum, but these processes may be distinguished by EIS as alterations in different frequency regions. While traditional chemical pre-treatments for enhanced hydrolytic stability perform excellent, they are being phased out from industrial applications due to environmental concerns and work health issues. Today there is an intense ongoing research regarding the mechanisms and performance of environmentally friendly pretreatments to develop systems of similar performance, and the analysis of the confined metal / polymer interface is crucial for this development. The capability of the integrated in situ ATR-FTIR Kretschmann and EIS set-up was therefore further applied to systems where a surface pre-treatment had been applied to the metal prior to the organic coating. Studies were first performed on vacuum-evaporated films of zinc treated with a titanium-based conversion coating and further coated with a UV-curing polymer. Alterations of the conversion layer could be detected upon exposure to the electrolyte. Also alkaline-cleaned aluminium coated with an amino-functional silane film and a thermo-curing epoxy top-coat was thoroughlycharacterized by both ATR-FTIR and IRRAS and further investigated upon exposure toelectrolyte and humid air. Changes at the hidden interface were detected upon thermal curingof the epoxy film and during exposure in electrolyte, and the in situ ATR-FTIR Kretschm annanalysis showed a high sensitivity towards alterations in the interfacial region. Complementary studies in the absence of metal could confirm a water uptake within the silane film and water-induced alterations of the siloxane network.
QC 20101222

The aim of this thesis work was to systematically investigate the physico-chemical properties of polyelectrolyte complexes (PECs) formed by bottle brush and linear polyelectrolytes in solution and at solid / liquid interfaces. Electrostatic self-assembly of oppositely charged macromolecules in aqueous solution is a versatile strategy to construction of functional nanostructures with easily controlled properties. Bottle brush architecture, introduced into the PEC, generates a number of distinctive properties of the complexes, related to a broad range of application, such as colloidal stability and protein repellency to name a few. To utilize these materials in a wide range of applications e.g. drug delivery, the understanding of the effects of polymer architecture and solution parameters on the properties of bottle brush PECs is of paramount importance. This thesis constitutes a systematic investigation of PECs formed by a series of cationic bottle-brush polyelectrolytes and a series of anionic linear polyelectrolytes in aqueous solution. The focus of the first part of the thesis was primarily on formation and characterization of PECs in solution, whereas the adsorption properties and adsorption kinetics of bottle-brush polyelectrolytes and their complexes was investigated in the second part of the thesis work. In particular, effects of the side-chain density of the bottlebrush polyelectrolyte, concentration, mixing ratio and molecular weigh of the linearpolyelectrolyte on formation, solution properties, stability and adsorption of PECs were addressed. The pronounced effect of the side-chain density of the bottle-brush polyelectrolyte on the properties of stoichiometric and nonstoichiometric PECs was demonstrated. Formation of PECs by bottle-brush copolymers with high density of side-chains results in small, watersoluble, molecular complexes having nonspherical shape, independent of concentration. Whereas formation of PEC-aggregates was revealed by bottle-brush polyelectrolytes with low side chain density, the level of aggregation in these complexes is controlled by polyelectrolyte concentration. The structure of the PECs formed with low molecular weight polyanions is consistent with the picture that several small linear polyelectrolyte molecules associate with the large bottle-brush. In contrast, when complexation occurs between polyanions of high molecular weigh and the bottle-brush polymers considerably larger PECs are formed, consistent with several bottle-brush polymers associating with one high molecular weight polyanion.
QC 20110516

Aqueous silica is present in all natural waters and exhibits a high affinity for the surfaces of iron oxides. Therefore, it is expected to play an important role in environmental systems. Experiments were conducted to investigate the fundamentals of silica sorption onto pre-formed ferric hydroxide at pH 5.0-9.5 and silica concentrations of 0-200 mg/L as SiO₂. Over the entire pH range studied, sorption densities exceeding monolayer sorption were observed at silica levels typical of natural waters. Under some circumstances, sorption exceeded a monolayer while the particle zeta potential remained positive, a phenomenon which is inconsistent with available models. To address this deficiency, an extended surface complexation model was formulated in which soluble dimeric silica sorbs directly to iron surface sites. This model fits sorption density data up to 0.40 mol SiO₂/mol Fe, and it accurately predicts trends in zeta potential and the observed H⁺ release during silica sorption to ferric hydroxide at pH 5.0 and 6.0.

A second phase of research was aimed at identifying the practical implications of silica sorption to iron hydroxide in natural and engineered systems. Two types of surfaces were prepared by exposing pre-formed Fe(OH)₃ to aqueous silica (0-200 mg/L as SiO₂) for periods of 1.5 hours or 50 days. The concentration of pre-formed iron passing through a 0.45 micron pore size filter at pH 6.0-9.5 increased as the solids aged in the presence of silica. Consistent with formation of small, stable colloids, "soluble" iron concentrations exceeded 0.2 mg/L only at zeta potentials < -15 mV. When arsenate was added to iron hydroxide particles equilibrated with silica for 1.5 hours, percentage arsenate removals were high. In contrast, arsenate removals decreased markedly as pH and silica concentrations increased if silica was pre-equilibrated with the iron for 50 days. Trends in percentage removal of humic substances were similar. Competition for sorption sites was the main cause of hindered anionic contaminant removal. However, interference with hydrolysis and precipitation are expected to be important under some circumstances, particularly during water treatment.
Master of Science

Friction forces between protein / polyelectrolyte layers, adsorption properties of proteins, and conformational changes due to variation in electrolyte concentration have been investigated. The aim was to obtain better understanding of adsorbed layer properties, with focus on the relation between layer structure and lubrication capabilities. The major techniques used were AFM (atomic force microscope) with colloidal probe for normal force and friction measurements together with QCM-D (quartz crystal microbalance with dissipation) for measurement of adsorption and conformational changes of adsorbed layers. A comparison between some techniques for calibration of the AFM instrument for friction measurements was made to find the most suitably one for colloidal probe friction measurements in aqueous solutions. It is suggested that the normal and torsional Sader methods are preferred in combination with torsional detector sensitivity measurement, for which one new methodology has been proposed. Adsorption was studied for bovine serum albumin, cytochrome c, myoglobin and mucin, whereas conformational changes of the adsorbed layer were monitored only for mucin. It was found that it was essential to take into account bulk density and viscosity changes for correct interpretations of QCM data when studying the effect of changes in electrolyte type and concentration on preadsorbed layers of mucin, and also when having different (high) concentrations of proteins in the measuring solution. The adsorbed amount of proteins appears to depend on the strength of the surface attachment, in such a manner that a too high affinity reduces the adsorbed amount. Friction properties in aqueous solution have been studied for adsorbed layers of PEO45MEMA:METAC co-polyelectrolytes, with varying density of grafted PEO45 side chains and varying charge density, as well as for a naturally occurring polyelectrolyte (chitosan) and the glycoprotein mucin. These polymers were used to cover a wide range of different types of adsorbed layers and interactions to gain a better understanding of friction mechanisms and demands on layer properties for achieving favourable lubrication. It was found that the common features of low friction layers are that no attractive forces are present, and that excluded volume and / or electrostatic forces counteract chain interpenetration under load.
QC 20100903

The principal objectives of this thesis are to introduce a new method, colloidal particle scattering (CPS), to measure colloidal and surface forces, and to demonstrate various applications of this method. CPS determines particle-particle interaction forces through creating particle collisions and extracting the interaction forces from the degree of asymmetry of the collision trajectories. Since the force to deflect a micron-sized particle is much smaller than that to deform a macroscopic spring or cantilever used in a commercial force apparatus, this new technique increases the resolution of force determination by four orders of magnitude.
Based on the CPS principles, we have built a force apparatus called "microcollider". It successfully determined the van der Waals forces and the electrostatic force between two 5 $ mu$m latex spheres at different salt concentrations. A "hairy" latex model was introduced to explain the measured van der Waals forces which are weaker than those predicted by theory assuming smooth latex surfaces. This is consistent with other experimental findings about the surfaces of latex particles.
A similar "hairy" model was applied to determine the adsorption layer thicknesses of two triblock copolymers adsorbed on latex particles. The results show that the configuration of the buoy block composed of polyethylene oxide (PEO) is more extended than a random PEO coil, which agrees with theoretical predictions. Moreover, excellent quantitative agreement between the adsorption layer thicknesses determined by CPS and other methods has been found.
Dynamic steric interactions between two high molecular weight PEO adlayers have also been studied. Both the elastic modulus and the adsorption layer thickness were determined. The results show that a thick layer has a lower elastic modulus than a thin one composed of the same polymer. This implies that an extended loop/tail structure in a thick layer is less stiff than a flat compact one in a thin layer, which is consistent with theory.
In addition, the microcollider can accurately determine particle-wall interactions as well. A rather weak electrokinetic lift force was measured. The results are in good agreement with the solutions rigorously derived from two new theories.

In Sweden the encapsulated nuclear waste will be surrounded by compacted bentonite in the granitic host rock. In contact with water-bearing fractures the bentonite barrier may release montmorillonite colloids that may be further transported in groundwater. If large amounts of material are eroded from the barrier, the buffer functionality can be compromised. Furthermore, in the scenario of a leaking canister, strongly sorbing radionuclides, can be transported by montmorillonite colloids towards the biosphere. This thesis addresses the effects of groundwater chemistry on the generation, stability, sorption and transport of montmorillonite colloids in water bearing rock fractures. To be able to predict quantities of montmorillonite colloids released from the bentonite barrier in contact with groundwater of varying salinity, generation and sedimentation test were performed. The aim is first to gain understanding on the processes involved in colloid generation from the bentonite barrier. Secondly it is to test if concentration gradients of montmorillonite colloids outside the barrier determined by simple sedimentation experiments are comparable to generation tests. Identical final concentrations and colloid size distributions were achieved in both types of tests. Colloid stability is strongly correlated to the groundwater chemistry. The impact of pH, ionic strength and temperature was studied. Aggregation kinetics experiments revealed that for colloid aggregation rate increased with increasing ionic strength. The aggregation rate decreased with increasing pH. The temperature effect on montmorillonite colloid stability is pH-dependent. At pH≤4, the rate constant for colloid aggregation increased with increasing temperature, regardless of ionic strength. At pH≥10, the aggregation rate constant decreased with increasing temperature. In the intermediate pH interval, the aggregation rate constant decreased with increasing temperature except at the highest ionic strength, where it increased. The relationship between the rate constant and the ionic strength allowed the critical coagulation concentration (CCC) for Na- and Ca-montmorillonite to be determined. In order to distinguish the contribution of physical filtration and sorption to colloid retention in transport, the different retention mechanisms were quantified. Sorption on different representative minerals in granite fractures was measured for latex colloids (50, 100, 200 nm) and montmorillonite colloids as a function of ionic strength and pH. Despite of the negative charge in mineral surfaces and colloids, sorption was detected. The sorption is correlated to the mineral point of zero charge and the zeta potential of the colloids, and increases with increasing ionic strength and decreasing pH. In transport experiments with latex colloids in columns packed with fracture filling material, the retention by sorption could clearly be seen. In particular at low flow rates, when the contact time for colloids with the mineral surfaces were the longest, sorption contributed to retention of the transport significantly. The retention of latex colloids appeared to be irreversible in contrary to the reversible montmorillonite colloid retention. Generation, stability and sorption of the montmorillonite colloids are controlled by electrostatic forces; hence, the results were in qualitative agreement with DLVO.

This thesis deals with the use of electric fields for evaluation and control of chemical systems. An electric field can result in the flow of charge across an interface between a metal and a solution, by means of chemical reactions. This interplay between electricity and chemistry, i.e. electrochemistry, is a field of crucial importance both within research and industry. Applications based on electrochemical principles encompass such diverse areas as batteries and fuel cells, pH electrodes, and the glucose monitor used by people suffering from diabetes.A major part of the present work concerns the use of static electric fields in solutions containing a non-contacted metal surface. In such a setup it is possible to control the extent of electrochemical reactions at different positions on the metal. This allows the formation and evaluation of various types of gradients on electrodes, via indirectly induced electrochemical reactions. This approach is a new and simple way of forming for instance molecular gradients on conducting surfaces. These are very advantageous in biomimetic research, because a gradient contains a huge amount of discrete combinations of for example two molecules. The basis for the technique is the use of bipolar electrochemistry. Briefly, a surface can become a bipolar electrode (an electrode that acts as both anode and cathode) when the electric field in the solution exceeds a certain threshold value, thereby inducing redox reactions at both ends. In our experiments, the driving force for these reactions will vary along the electrode surface. Since the result of an electrochemical reaction can be the deposition or removal of material from an electrode, bipolar electrochemistry can be used to create gradients of that material on a surface. In order to gain a deeper understanding of these processes, the potential and current density distributions at bipolar electrodes were investigated with different methods. Especially the use of imaging techniques was important for the visualization and analysis of the gradients. Using this knowledge, the formation of more complex gradients was facilitated, and the results were further compared to simulations based on simple conductivity models. These simulations also provided us with means to predict the behavior of new and interesting setup geometries for pattering applications.The other major part is more application driven and deals with the use of alternating electric fields for chemical analysis, a technique known as electrochemical impedance spectroscopy (EIS). In this work, EIS has been applied for the analysis of engine oils and industrial cutting fluids. Emphasis was placed on practical aspects of the measurement procedure, and on the evaluation of the results using statistical methods. It was for example shown that it was possible to simultaneously determine the amount of different contaminants in low conducting solutions. Generally, EIS is used to measure the impedance of a solution or a solid, often as a function of the frequency of the alternating electric field. The impedance of a system is closely correlated to its complex dielectric constant, and EIS can therefor be used to examine many chemical and physical processes. It is further well suited for characterizing low conducting media with little or no redox-active species. The evaluation of impedance data is often a quite complex task, which is why we have made use of statistical methods that drastically reduce the effort and quickly reveal significant intrinsic parameters.

The primary focus of this work is to develop an understanding of crystallisation in hard sphere systems. The thesis is presented in two parts. The first section is an investigation of the liquid/crystal interface at equilibrium using molecular dynamical simulations. The objective is to understand how the interface might bridge between the disordered and ordered states in liquid/crystal environments. Topological measures of structure are used to investigate whether any precursor structures are present in the liquid phase, close to the interface, that would allow transition from disorder to order. This differs from other work where simpler measures of structure, classifying phases into either liquid or crystal, are used. The results indicate that the liquid/crystal interface of a hard sphere system is very narrow and no readily observable structures were found that extended past the width of the equilibrium interface. The second section of the thesis is a theoretical study of growth kinetics in hard sphere systems using density functional theory. The kinetics in a fixed volume are examined with a single conserved order parameter. The work is extended incorporating both conserved particle and non-conserved structure dynamics. The kinetics of growth are examined and it is shown that the small initial crystals are quickly isolated from the higher pressure of the surrounding system through the development of a depletion zone.

The aim of this thesis work was to gain understanding of the interactions between talc mineral and surfaces, liquids and chemicals relevant for industrial applications, such as pulp and paper. Talc is used in the pulp and paper industry as a filler pigment, in control of pitch (lipophilic extractives) deposits and as a coating pigment. A deeper understanding of talc interactions will be beneficial in optimizing its use. Long-range attractive interactions between talc and hydrophobic model probes, as well as pitch probes, have been measured using the atomic force microscope (AFM) colloidal probe method. Two procedures for preparation of pitch colloidal probes were developed to allow these studies. Model hydrophobic, nanorough surfaces with surface energy characteristics similar to talc have also been prepared and their interactions with hydrophobic model probes compared to interactions between hydrophobic model probes and talc. It is demonstrated that talc mineral interacts with model hydrophobic particles, as well as with pitch, by long-range attractive forces, considerably stronger than the expected van der Waals force. The possible origin of the measured interaction forces is discussed, and the conclusion is that the main cause is an attractive capillary force due to formation of a gas/vapor capillary between the surfaces. Force measurements using model hydrophobic, nanorough surfaces show that a large-scale waviness does not significantly influence the range and magnitude of the capillary attraction, but large local variations in these quantities are found. It is demonstrated that a large variation in adhesion force corresponds to a small variation in local contact angle of the capillaries at the surfaces. The nature of the surface topographical features influences the capillary attraction by affecting the local contact angle and by pinning of the three-phase contact line. The effect is clearly dependent on the size of the surface features and whether they exist in the form of crevices or as extending ridges. Entrapment of air also affects the imbibition of water in pressed talc tablets. The effects of wetting and dispersion agents on the interactions between talc and hydrophobic probes have also been investigated. It is demonstrated that a common dispersing agent used for talc, poly(acrylic acid), does not affect the capillary attraction between talc and non-polar probes. In fact, the results strongly suggest that poly(acrylic acid) does not adsorb on the basal plane of talc. From this finding it is inferred that the stabilizing effect of this additive most likely is due to adsorption to the edges of talc. In contrast, a wetting agent (the non-ionic triblock copolymer Pluronic PE6400) removes the long-range capillary attraction. It is suggested that such an ability to replace air at the talc surface is of great importance for an efficient wetting agent. The Hamaker constant for talc has also been estimated by using optical data obtained from spectroscopic ellipsometry. It is demonstrated that a nanocrystalline talc mineral, cut in different directions displays very small differences in Hamaker constant between the different crystallographic orientations, whereas a microcrystalline sample displays a significantly higher value. The estimated Hamaker constants are discussed for different material combinations of relevance for the pulp- and paper industry, such as cellulose and calcium carbonate.
Målet med detta avhandlingsarbete var att öka förståelsen för interaktioner mellan talkmineral och ytor, vätskor och kemikalier relevanta för industriella applikationer, såsom papper och massa. Talk används i pappers- och massaindustrin som fyllmedel, för kontroll av hartsrika (lipofila extraktivämnen) avsättningar och som bestrykningspigment. En djupare förståelse för talkinteraktioner kommer att vara användbart för att optimera dess användning. Långväga attraktiva interaktioner mellan talk och hydrofoba modellpartiklar, såväl som mellan talk och hartspartiklar, har uppmätts med hjälp av atomkraftsmikroskopi (AFM) genom att fästa kolloidala partiklar på kraftsensorn. Två metoder för att framställa partiklar gjorda av harts har utvecklats för att möjliggöra dessa studier. Hydrofoba, nanostrukturerade modellytor med ytenergier liknande de för talk har också tillverkats och deras växelverkan med hydrofoba modellpartiklar har jämförts med dem mellan talk och hydrofoba modellpartiklar. Studierna visar att talkmineral växelverkar med hydrofoba modellpartiklar, såväl som med harts, genom långväga attraktiva krafter som är betydligt starkare än den förväntade van der Waals kraften. Möjliga orsaker till de uppmätta växelverkanskrafterna diskuteras och slutsatsen blir att huvudorsaken är en attraktiv kapillärkraft som uppkommer genom att en gas-/ångkapillär bildas mellan ytorna. Kraftmätningar gjorda med hydrofoba nanostrukturerade modellytor visar att en storskalig vågighet inte nämnvärt påverkar storleken av kapillärattraktionen, men stora lokala variationer existerar. Det demonstreras att en stor variation i adhesionskraft motsvaras av en liten variation i lokal kontaktvinkel för kapillärerna på ytorna. Ytornas topografi påverkar kapillärattraktionen genom att påverka den lokala kontaktvinkeln samt genom att trefaskontaktlinjen inte kan röra sig fritt över ytan. Effekten är tydligt beroende av huruvida ytojämnheterna existerar i form av nedsänkningar eller upphöjningar. Instängd luft påverkar också pressade talktabletters uppsugningsförmåga av vatten. Vätnings- och dispergeringsmedels inverkan på växelverkan mellan talk och hydrofoba partiklar har undersökts. Resultaten visar att ett vanligt dispergeringsmedel för talk, polyakrylsyra, inte påverkar kapillärattraktionen. I själva verket tyder data på att polyakrylsyra inte adsorberas på talks basalplan. Utifrån dessa resultat dras slutsatsen att polyakrylsyra stabiliserar talkdispersioner genom att adsorbera på talkkanterna. Ett vanligt vätmedel (nonjonisk triblock sampolymer Pluronic PE6400) tar å andra sidan bort långväga kapillärattraktion. Detta antyder att egenskapen att ersätta luft på talkytan är av stor betydelse för effektiva vätmedel. Hamakerkonstanten för talk har uppskattats genom att utnyttja optiska data från ellipsometrimätningar. Det demonstreras att ett nanokristallint talkmineral kapat i olika riktningar uppvisar mycket små skillnader i Hamakerkonstant mellan de olika kristallografiska orienteringarna, medan ett mikrokristallint prov uppvisar ett betydligt högre värde. De beräknade Hamakerkonstanterna diskuteras för olika materialkombinationer relevanta för pappersindustrin, såsom cellulosa och kalciumkarbonat.
QC 20100813

Chitin crystallites were prepared from crab chitin using HCl hydrolysis. On avenge, the surface charge density of the chitin crystallites was calculated to be 0.5 e/nm2 based on conductimetric titration data. The formation of a chiral nematic phase in aqueous suspensions of chitin crystallites and the in situ texture of the crystallite suspensions were investigated using polarised optical microscopy and freeze-fracture transmission electron microscopy. The effect of the interparticle electrostatic interaction on phase separation has been explored through phase diagrams and the interaction energy was calculated based on experimental zeta potentials. The flow properties of the liquid crystalline phases of chitin crystallites have been studied rheologically. Shear thinning behaviour and a two-regime flow curve were observed for isotropic suspensions and biphasic suspensions respectively. A typical three-regime flow curve for liquid crystalline polymers was found for the anisotropic suspension of chitin crystallites. The maximum in the viscosity-concentration curve was found at the phase transition concentration: isotropic to biphasic. Chitin crystallites were systematically deacetylated using NaOH hydrolysis. It was found dud the reaction was pseudo first order. These modified crystallites are highly charged. Their phase behaviour contradicts the theoretical prediction by Stroobants et al. in addition, crystallites with a different extent of N-sulfonation were obtained in an aqueous medium using triethylamine/sulfur trioxide (TEA/SO3) by controlling the TEA/SO3 concentration used in the reaction. The colloidal behaviour of the suspension of the N-sulfonated crystallites was studied by plotting the zeta potential of the suspension as a function of the pH. Once the extent of N-sulfonation reached a certain level (80% or above), the chiral nematic; phase formed while below this level only the nematic phase was observed. TEM studies showed that the crystallites were wel

With increasing environmental awareness, the desire to protect human beings and the environment from adverse effects induced by dispersed metals has become an issue of great concern and interest. New policies, such as REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) within the European Community, have been implemented to reduce hazards posed by the use of chemicals on producers and downstream users. The generation of exposure assessment data and relevant test procedures able to simulate realistic scenarios are essential in such legislative actions. This doctoral study was initiated to fill knowledge gaps related to the metal release process of stainless steels. A wide range of stainless steel grades, fourteen in total, were investigated. They cover a very broad range of applications, and the focus in the thesis was to simulate a few selected exposure scenarios: precipitation, the human body and food intake. Comparisons were made between metal release from stainless steel alloys and the pure metals that constitute each stainless steel in order to explore the differences between alloys and pure metals, and to provide quantitative data on metal release rates of different alloy constituents. Because of similar surface properties between stainless steel and pure chromium, this metal exhibits similar release rates, whereas iron and nickel exhibit significantly lower release rates as alloy components than as pure metals. Detailed studies were also performed to elucidate possible relations between metal release and steel surface properties. Key parameters turned out to be chromium enrichment of the self-passivating surface film, surface roughness, the electrochemically active surface area and the microstructure of the steel substrate. The degree of metal release increased with decreasing chromium content in the surface oxide, increasing surface roughness, and increasing presence of inhomogeneities in the bulk matrix. More detailed studies were initiated to possibly correlate the nucleation of metastable pits and the extent of metal release. Evidence was given that metastable pits exist even when the stainless steel is passive, and may cause extremely short-lived bursts of released metal before the surface film repassivates again.
QC 20100810

This thesis examines the effect of lead sulphide (PbS) CQDs' surface chemistry and interfaces to their photovoltaic performance. Using PbS CQDs as the starting material, cation-exchange was utilised to form PbS/CdS core/shell CQDs, which were thoroughly characterised and the improved surface passivation was shown by increased photoluminescence yield and lifetime. The core/shell CQDs were incorporated into a ZnO/CQD heterojunction solar cell device and showed a substantial improvement of the mean open-circuit voltage (Voc), from 0.4 V to 0.6 V, over PbS reference devices. By optimising shell thickness and surface ligands, core/shell CQD devices with average device efficiency of 5.6 % were fabricated as compared to 3.0 % for unshelled PbS devices. The lower defect density due to better passivation confers lower carrier density in core/shell CQD film. To take advantage of low defect concentration and to aid charge extraction, a 3 dimensional quantum funnel concept was sought of by blending two populations of PbS/CdS CQDs of different sizes. By incorporating a blend component within a heterojunction device, even when the device thickness is beyond what is optimal for the depletion width and the diffusion length of the system, high Voc is still maintained. In a separate study, a p-i-n device strategy was examined, and with this approach, a maximum device efficiency of 6.4 % was achieved. Despite the improvements made to Voc by optimizing surface passivation, fill factors of the devices are low. By using poly(3-hexylthiophene-2,5-diyl) (P3HT) as a hole transport material (HTM), fill factor and the overall performance improved over a reference device without the HTM. Further studies showed that oxidation of the HTM material results in increased p-type characteristic, thus optimising hole transport. This beneficial oxidation process also makes the device air-stable. From this, devices of up to 8.1 % efficiency and devices with fill factor as high as 0.72 were fabricated.

The cellular response to a biomaterial, such as a dental implant, is mainly governed by the surface properties, and can thus be altered by the introduction of a surface coating. In this thesis the buildup of a biomacromolecule-based coating formed by layerby-layer (LbL) deposition of the charged polypeptides poly(L-lysine) (PLL) and poly(L-glutamic acid) (PGA) has been studied. In an attempt to make these coatings bioactive and useful for bone-anchored implants, an amelogenin protein mixture (EMD), has been immobilized in these thin polyelectrolyte multilayer (PEM) films. Multilayers were also built by LbL deposition of the natural biomacromolecules collagen (Col) and hyaluronic acid (HA). Multilayer films of these two extra-cellular biomacromolecules should be of interest for use as a scaffold for tissue engineering.

The buildup of the multilayer films has been followed in situ, using ellipsometry, quartz crystal microbalance with dissipation (QCM-D), and dual polarization interferometry (DPI). The studied PLL/PGA multilayers were found to be highly hydrated, and to exhibit a two-regime buildup behavior, with an initial “slow-growing” regime, and a second “fast-growing” regime with a linear growth in film thickness and more than linear growth in mass. A net diffusion of polypeptides into the film during the buildup led to an increase in density of the films for each layer adsorbed. A change in density was also observed in the Col/HA film, where HA penetrated and diffused into the porous fibrous Col network.

The formed PLL/PGA films were further found to be rather stable during drying, and post-buildup changes in temperature and pH, not losing any mass as long as the temperature was not raised too rapidly. The film thickness responded to changes in the ambient media and collapsed reversibly when dried. A swelling/de-swelling behavior of the film was also observed for changes in the temperature and pH.

The EMD protein adsorbed to silica surfaces as nanospheres, and could by itself form multilayers. The adsorption of EMD onto PLL/PGA multilayer films increased at lower pH (5.0), and EMD could be immobilized in several layers by alternate deposition of EMD and PGA.

This thesis is about the molecular structure of minerals, their surface modification and the dispersion of selected minerals of a ceramic nature as sols and gels. The theme that permeates through this work and connects the different elements of the work is the search for fundamental knowledge and understanding of mineral structure and mineral surface structure. The underlying principal is that of molecular structure of surfaces and the changes in that molecular structure through modification of the surfaces. There are seven research divisions of study reported in this thesis: (A) Molecular structure and spectroscopy ofkaolinite (B) Molecular surface structure modified through intercalation with polar molecules (C) Molecular surface structure modified through intercalation with potassium and cesium acetates (D) Structure and spectroscopy of alumina phases and colloids (E) Structure and spectroscopy of titania and zirconia colloids (F) Synthesis, characterisation and spectroscopy of double layered hydroxides (hydrotalcites) (G) Spectroscopic and molecular structural studies of selected minerals of interest

Thesis (Ph. D.)--University of California, Riverside, 2009.
Includes abstract. Available via ProQuest Digital Dissertations. Title from first page of PDF file (viewed March 12, 2010). Includes bibliographical references (p. ). Also issued in print.

The primary focus of this work is to develop an understanding of crystallisation in hard sphere systems. The thesis is presented in two parts. The first section is an investigation of the liquid/crystal interface at equilibrium using molecular dynamical simulations. The objective is to understand how the interface might bridge between the disordered and ordered states in liquid/crystal environments. Topological measures of structure are used to investigate whether any precursor structures are present in the liquid phase, close to the interface, that would allow transition from disorder to order. This differs from other work where simpler measures of structure, classifying phases into either liquid or crystal, are used. The results indicate that the liquid/crystal interface of a hard sphere system is very narrow and no readily observable structures were found that extended past the width of the equilibrium interface. The second section of the thesis is a theoretical study of growth kinetics in hard sphere systems using density functional theory. The kinetics in a fixed volume are examined with a single conserved order parameter. The work is extended incorporating both conserved particle and non-conserved structure dynamics. The kinetics of growth are examined and it is shown that the small initial crystals are quickly isolated from the higher pressure of the surrounding system through the development of a depletion zone.

The aim of this work is to study the interfacial properties of amphiphilic compounds at the liquid–air interface in an attempt to develop a comprehensive understanding of their orientation as well as the influence of their interaction with the solvent on the interfacial layer properties. Using Vibrational Sum Frequency Spectroscopy (VSFS) as the main tool, the molecular structure of the amphiphilic layer and the amphiphile–solvent relation can be illuminated in great detail – it is arguably the most sensitive surface spectroscopy currently available. Due to its second order nature, the VSFS technique is capable of distinguishing molecules at the interface even in the presence of a vast excess of similar molecules in the bulk.Ionic liquids (Ils) form a class of solvent which are increasingly receiving attention as ``green solvents´´. Some of these, such as ethyl ammonium nitrate (EAN), a protic IL, have the capacity to hydrogen bond extensively which is one of the important features they share with water. Since the interaction with solvent is an important consideration for self assembly and it is known that surfactant self assembly in the EAN bulk is analogous to in water, it was considered of interest to probe self assembly at EAN–air interface. To this end the interfacial structure of the pure EAN interface was probed, as was the conformation and ordering of nonionic surfactants. These studies reveal that EAN is highly ordered at the interface, exposing the ethyl moiety to the gas phase. Additionally, polarization studies have enabled the average orientation of the ethyl group to be determined. Adsorption of nonionic surfactants at the interface appears to significantly displace the EAN from the interface. The headgroup of the surfactant, a linear ethylene oxide group, appears to be highly disordered.The disorder of the linear ethylene oxide groups has led to difficulties in their surface spectroscopic fingerprinting in this and other works. In an attempt to study the interfacial behaviour of ethylene oxide and the temperature dependence of its hydration, closed loop structures of PEO attached to hydrophobic groups were also probed. This essentially locks their conformation. Such molecules are known as crown ethers and display interesting interfacial behaviour and also the ability to bind cations. The presence of even small amounts of adsorbed crown ethers at the water interface is shown to considerably perturb the water structure. The NO, CN, COC and CH vibrational modes of these compounds at the air-water interface as well as OH vibrational modes of the surface water hydrating this compound have been targeted in order to obtain molecular information about arrangement and conformation. The CH2 vibrational modes of crown ethers have been identified and found to be split due to their interaction with ether oxygen. The spectra provide evidence for the existence of a protonated crown complex moiety at the surface leading to the appearance of strongly ordered water species. The orientation of Nitrobenzo crown (NB15C5) was monitored as a function of solution concentration, by targeting the ratio of peak intensities of the CN and NO2 vibrational modes. The water of hydration has also been probed as a function of crown concentration, salt concentration, and temperature. The latter study strongly suggests that the surface can be treated as a charged interface, and that the associated ordered water decreases with increasing ionic strength of the bulkFinally, insoluble monolayers of fatty acids spread on a water surface have also been studied in an effort to further understand the relationship between molecular architecture and film structure. Fatty acid (Arachidic Acid – AA and Eicosenoic Acid – EA) monolayers are compared to investigate the effect on the monolayer structure of introducing unsaturation into the alkyl chain. For AA, at very large area per molecule, floating domains of crystalline nature exist rather than any classical gaseous phase. The measured conformational disorder in EA decreases continuously with monolayer compression and no crystalline domains are observed at low density. Addition of NaCl to the subphase does not affect the monolayer order for either of the compounds; instead, a dramatic increase in the signal of the water hydrating the headgroups is observed. The effect of introducing further unsaturations (up to three) was also studied in order to probe the resulting interfacial structure. Remarkably the double bonds appear to adopt the same orientation, irrespective of how many they are in the chain. By monitoring the vinyl CH stretch it was possible to study the film stability towards oxidative degradation and it was found that all three unsaturated species studied showed rapid degradation. The rate of degradation could be controlled by adjusting the film pressure. However, the monolayers could be stabilised by performing the experiments in an inert nitrogen atmosphere.
QC20100629

Thesis (MSc)--Stellenbosch University, 2003.
ENGLISH ABSTRACT: In this thesis the formation and properties of a polymer gel on and at a surface are investigated. The gel under investigation is defined as a three-dimensional network of macromolecules that form permanent links with one another and also with confining planar surfaces. The precise location of the crosslinks on the wall or on another macromolecule is not known prior to linking, and will differ from sample to sample. However, once the crosslinks are formed, they are assumed to be permanent. This random linking is the source of the disorder in the system, over which a quenched average has to be taken. An existing model [9] of network formation, with polymer-polymer crosslinks, is extended to incorporate a surface and polymersurface crosslinks. Within the framework of replica theory, statistical averages and physical properties of the system are calculated by means of a variational approach. Macroscopic information, in terms of the free energy of deformation, is obtained by using two different potentials to simulate the erosslinks mathematically.
AFRIKAANSE OPSOMMING: In hierdie tesis word die vorming en eienskappe van 'n polimeergel, wat teen 'n oppervlak gevorm word, ondersoek. Die gel word gedefinieer as 'n drie-dimensionele netwerk van makromolekules wat permanente bindings met mekaar, maar ook met twee inperkende, platvlakke, vorm. Die presiese ligging van die bindings op die muur en op ander makromolekules is nie vooraf bekend nie, en sal verskil van een gel-monster tot die volgende. Sodra die konneksies egter gevorm is, word aanvaar dat hulle permanent is. Die lukrake bindingsproses is die oorsprong van wanorde in die sisteem, waaroor 'n wanorde-gemiddelde bereken moet word. 'n Bestaande model [9]van netwerkvorming, met polimeer-polimeer bindings, word uitgebrei om 'n oppervlakte en polimeer-oppervlak bindings in te sluit. Statistiese fisika gemiddeldes en fisiese eienskappe van die sisteem word binne die raamwerk van replika-teorie en 'n variasie benadering bereken. Makroskopiese inligting, in terme van die vrye energie van vervorming, word verkry deur twee verskillende potensiale te gebruik om die konneksies wiskundig voor te stel.

Colloidal particles suspended in a liquid or gas phase often interact with a solid-liquid or solid-gas interface. In this study, experimental data through atomic force microscopy and neutron reflectometry and theoretical results of colloidal particle-surface interactions were obtained and compared. Atmospheric and aquatic environments were considered for the interactions of microbial colloidal particles and nano-sized silica particles with planar surfaces. Spores of Bacillus thuringiensis, members of the Bacillus cereus group, were examined as the microbial particles, simulating the pathogens Bacillus cereus and Bacillus anthracis which are potentially dangerous to human health. Model planar surfaces used in this study include gold which is an electrically conductive surface, mica which is a highly charged, nonconductive surface, and silica. In atmospheric systems, the interaction forces were found to be strongly affected by the relative humidity, and the total adhesion force of a particle onto a surface was modeled as the addition of the capillary, van der Waals, and electrostatic forces. Each component is influenced by the properties of the particle and surface materials, including hydrophobicity and surface roughness, as well as the humidity of the surrounding atmosphere. In aquatic systems, the interaction forces are mainly affected by the solution chemistry, including pH and ionic strength. The main components of the interaction force between a microbial colloidal particle and a planar surface were found to be the van der Waals and electrostatic forces. The results obtained in this research provide insights into the fundamental mechanisms of colloidal particle interactions with environmental surfaces in both atmospheric and aquatic systems, contributing to the understanding of the phenomena driving such interfacial processes as deposition, aggregation, and sedimentation. Thus, the results can help us describe the behavior of contaminant colloidal particles in environmental systems and subsequently devise better means for their removal from environmental surfaces.

In the research presented in this licentiate thesis the surface specific technique Vibrational Sum Frequency Spectroscopy, VSFS, combined with the Langmuir trough has been utilized to investigate Langmuir monolayers and Langmuir-Blodgett (LB) deposited mono- and bilayers of phospholipids. Their molecular structure, stability, and hydration were probed to gain additional understanding of important properties aiming at facilitating the use of such layers as model systems for biological membranes.

VSFS was applied to in situ studies of the degradation of Langmuir monolayers of 1,2-diacyl-phosphocholines with identical C-18 chains having various degrees of unsaturation. The time-dependent change of the monolayer area at constant surface pressure as well as the sum frequency intensity of the vinyl-CH stretch at the C=C double bonds were measured to monitor the degradation. It was shown that a rapid degradation of the monolayers of unsaturated phospholipids occurred when exposed to the laboratory air compared to the fully saturated lipid, and that the degradation could be inhibited by purging the ambient air with nitrogen. The degradation was attributed to oxidation mediated by reactive species in the air.

The molecular structure and order of Langmuir monolayers of 1,2-distearoyl-phosphocholine (18:0 PC) and their hydrating water were investigated at different surface pressures using VSFS. The spectroscopic data indicated a well ordered monolayer at all surface pressures with a more intense signal at higher pressures attributed to the subsequent increase of the number density and more ordered lipid molecules due to the tighter packing. Water molecules hydrating the headgroups or being in contact with the hydrophobic parts were observed and distinguished by their vibrational frequencies, and found to have different average orientations.

Additionally, monolayers of 18:0 PC, its fully deuterated analogue, and 1,2-distearoyl-phosphoserine (18:0 PS) were Langmuir-Blodgett (LB) deposited on CaF₂ substrates and VSFS was used to investigate the structure and order of the films as well as the hydrating water. The CH-region, water region, and lower wavenumber region containing phosphate, ester, carboxylic acid, and amine signals were probed to obtain a complete picture of the molecule. The data indicates that all deposited monolayers formed a well ordered and stable film and the average orientation of the aliphatic chains was determined using the antisymmetric methyl stretch.

I forskningen som presenteras i denna licentiatavhandling har den ytspecifika vibrationssumfrekvensspektroskopin, VSFS, använts tillsammans med Langmuirtråget för att studera Langmuir-monolager och Langmuir-Blod-gett (LB) deponerade monolager och bilager av fosfolipider. För att utvidga förståelsen av egenskaper som är viktiga för att underlätta användandet av dem som modellsystem för biologiska membran undersöktes såväl deras molekylära struktur som stabilitet och hydratisering.

VSFS användes för att genomföra in situ-studier av nedbrytningen av Langmuir-monolager av 1,2-diacyl-fosfokoliner med identiska 18 kolatomer långa sidokedjor med varierande antal omättade kol-kol-bindningar. För att övervaka nedbrytningen mättes såväl den tidsberoende förändringen av monolagernas area vid konstant yttryck som sumfrekevensintensiteten från dubbelbindningarnas CH-vibration. När monolagerna bestående av omättade fosfolipider utsattes för laboratorieluften bröts de ner hastigt jämfört med det helt mättade monolagret. Denna nedbrytning som sannolikt orsakades av reaktiva ämnen i luften kunde inhiberas fullständigt genom att ersätta den omgivande luften med kvävgas.

Den molekylära strukturen och ordningen hos Langmuir-monolager av 1,2-distearoyl-fosfokolin (18:0 PC) och deras hydratiseringsvatten undersöktes vid olika yttryck med VSFS. Den spektroskopiska datan visar att monolagerna är välordnade vid alla yttryck samt att sumfrekvenssignalens styrka ökar med ökande yttryck på grund av såväl det större antalet molekyler per ytenhet som den högre ordningen då molekylerna packas tätare. Vattenmolekyler som hydratiserar huvudgrupperna eller är i kontakt med hydrofoba delar och har olika medelorientering observerades och kunde identifieras genom sina vibrationsfrekvenser.

Vidare deponerades monolager av 18:0 PC, dess fullt deuterade analog och 1,2-distearoyl-fofsfoserin (18:0 PS) på substrat av CaF₂ och VSFS användes för att undersöka filmernas struktur och ordning såväl som hydratiseringsvattnet. CH- och vattenregionerna samt lågvågtalsområdet som innehåller fosfat-, ester-, karboxylsyra- och aminsignaler undersöktes för att få en fullständig bild av den molekylära strukturen. Data visar att alla deponerade monolager bildade en välordnad och stabil film och kolvätekedjornas medelorientering bestämdes med hjälp av signalen från den antisymmetriska metylvibrationen.

QC 20100924

In this thesis the structure and hydration of small organic and amphipilic compounds adsorbed at the air-liquid interface, have been studied using the nonlinear optical technique Vibrational Sum Frequency Spectroscopy (VSFS). The second order nature of the sum frequency process makes this technique particularly surface sensitive and very suitable for interfacial studies, as molecules at the surface can be distinguished even in the presence of a vast excess of the same molecules in the bulk. Particular emphasis was given to the surface water structure and how it is affected by the presence of small model compounds such as acetic acid and formic acid, and also non-ionic surfactants with sugar based and ethylene oxide based polar headgroups. Understanding the structure of water at these interfaces is of considerable fundamental importance, and here VSFS provided unique information. Upon addition of tiny amounts of these surface active compounds, the ordered surface structure of water was found to be significantly perturbed, as revealed by the changes observed in the characteristic spectroscopic signature of the dangling OH bond of water molecules, which vibrate free in air and are present in the top monolayer. Dramatic differences between the different compounds were also observed in the bonded OH region, providing a valuable insight into the hydration of polar groups at interfaces. Additionally, by employing different polarization combinations of the laser beams involved in the sum frequency process, information about the different water species present at the surface and their average orientation were extracted. In particular an unusual state of water was found with a preferred orientation in a non-donor configuration in close proximity to the hydrophobic region formed by the hydrocarbon tails of the surfactant molecules.

The conformation and orientation of the different adsorbates were also characterized, targeting their specific vibrational frequencies. Noteworthy is the orientation of the fluorocarbon chain of ammonium perfluorononanoate (APFN), which in contrast to the hydrocarbon chains of the other surfactant molecules studied, remained constant over a wide range of surface densities. This behaviour was also observed for the anionic headgroup of sodium dodecyl sulphate (SDS). Other interesting findings were the formation of a cyclic dimer bilayer at the surface of concentrated aqueous solutions of acetic acid and the water structuring effect induced by poly(ethylene-oxide) headgroups, in spite of being themselves disordered at the air-liquid interface.

Underfill material is a special colloidal dispersion system with silicon dioxide particles in the organic liquid. It is used to improve the reliability of integrated circuits (IC) packaging in the microelectronics. In order to successfully synthesize the nanocomposite underfill meeting the requirements of the chip package, it is necessary to have a fundamental understanding about the particle stability in the non-aqueous liquid and the relationship between materials properties and interphase structure in the composite. The results of this thesis contribute to the knowledge of colloidal dispersion of nanoparticles in organic liquid by systematically investigating the effects of particle size, particle surface chemistry and surface tension, and liquid medium polarity upon the rheological and thermal mechanical properties of underfill materials. The relaxation and dielectric properties studies indicate that the polymer molecular chain motion and polarization in the interphase region can strongly influence the material properties of nanocomposite, and so a good interaction between particle and polymer matrix is key. With this study, a potential nanocomposite underfill can be synthesized with low viscosity, low thermal expansion, and high glass transition temperature. The excellent transmittance of nanoparticles leads to further investigation of their ability as reinforcing filler in the photo-curable polymer.

This thesis presents an investigation of the dynamic properties of wide range of interfacial systems, from colloidal particles in solution, through the realm of aerosols and onto studies of molecular adsorption at an interface. The primary experimental technique utilized is optical tweezers. An exploration of the history of the use of radiation pressure to manipulate matter is presented, followed by an introduction to how optical tweezers work. Some of the more advanced methods of tweezing are discussed, with an emphasis on the use of spatial light modulators (SLMs) to realise dynamic holographic optical tweezers (DHOTs), an example of which has been constructed within our laboratory using off-the-shelf optical components, and combined with a spectrometer to facilitate high resolution spectroscopic studies of microscopic systems. The spectroscopic analysis of microparticles is greatly enhanced by optical feedback generated when the wavelength of light utilized is an integer number of wavelengths around the circumference of the microsphere. Enhanced signal occurs at these wavelengths, termed whispering gallery modes (WGMs). The absolute position of these resonances depends strongly upon the shape, size and refractive index of the particle, and is predicted by Mie theory. A discussion of the concepts behind Mie theory, as well as how to use an experimental WGM spectrum to deduce the size and composition of a microparticle, is provided. This technique is then put to use in a detailed study on the properties of single aerosols, comprised of sodium chloride solution, and generated using a handheld medical nebulizer. Studies have been carried out on both evaporating and growing droplets trapped with a Gaussian beam; in the latter case, periods of size stability are observed, owing to resonant absorption of radiation at the trapping laser wavelength. The SLM can be used to change the trapping laser to a Laguerre-Gaussian (LG) mode, and an investigation of how this affects the dynamics of the droplet is presented. It is found that the use of LG modes with $ellgeq10$ produced Raman spectra with significantly more intense WGMs, and also suppressed droplet evaporation. Through observations made with fluorescent polystyrene microspheres, it is argued that the LG modes are more efficient at coupling into WGMs of the droplets. Leading on from these experiments on salt water droplets, experiments have been conducted using ionic liquids (ILs). These fluids have many fascinating properties and potential applications. The optical trapping of droplets comprised of aqueous solutions of the ionic liquid ethylammonium nitrate (EAN) and water has been demonstrated for the first time. These droplets are analysed spectroscopically by illuminating them with the output from a broadband LED; WGMs that are observed in the backscattered light are used to determine their size and composition. The response of the droplets to conditions of varying relative humidity has also been investigated. In order to characterise the relative humidity experienced by both the salt water and IL droplets, the concentration of water vapour within the trapping cells has been measured using diode laser absorption spectroscopy. The spatially modulated laser beam is then utilized in a different fashion; instead of optically tweezing a sample, a low numerical aperture objective lens is utilized to focus the laser onto the surface of a gold coated microscope slide. When a colloidal sample is placed on this surface, the thermal gradients cause the particles to form two dimensional crystals. The SLM is utilized to form multiple nucleation sites, and the dynamics of the crystals are directly observed in real time using video microscopy. It is found that grain rotation-induced grain coalescence (GRIGC) occurs, with the rotation of both crystals before coalescence. Control over the grain size is achieved by altering the separation of the laser spots, and shows that the time scale for grain boundary annealing in our system is in good agreement with theoretical expressions formulated for nanocrystal growth. Finally, as a complimentary technique to the microparticle spectroscopy previously discussed, a bulk interface is probed by using evanescent wave broadband cavity enhanced absorption spectroscopy (EW-BBCEAS) specifically to study the adsorption of cytochrome c (cyt c) to a fused silica surface. Visible radiation from a supercontinuum source is coupled into an optical cavity consisting of a pair of broadband high reflectivity mirrors, and a total internal reflection (TIR) event at the prism/water interface. Aqueous solutions of cyt c are placed onto the TIR footprint on the prism surface and the subsequent protein adsorption is probed by the resulting evanescent wave. The time integrated cavity output is directed into a spectrometer, where it is dispersed and analysed. The broadband nature of the source allows observation of a wide spectral range (ca 250 nm in the visible). The system is calibrated by measuring the absorption spectra of dyes of a known absorbance. Absorption spectra of cyt c are obtained for both S and P polarized radiation, allowing information about the orientation of the adsorbed protein to be extracted.

This thesis focuses on the study of the interactions between polyelectrolytes and surfactants in aqueous solutions and at interfaces, as well as on the structural changes these molecules undergo due to that interaction. Small–angle neutron scattering, dynamic, and static light scattering were the main techniques used to investigate the interactions in bulk. The first type of polymer studied was a negatively charge glycoprotein (mucin); its interactions with ionic sodium alkyl sulfate surfactants and nonionic surfactants were determined. This system is of great relevance for several applications such as oral care and pharmaceutical products, since mucin is the main component of the mucus layer that protects the epithelial surfaces (e.g. oral tissues). Sodium dodecyl sulfate (SDS) on the other hand, has been used as foaming agent in tooth pastes for a very long time. In this work it is seen how SDS is very effective in dissolving the large aggregates mucin forms in solution, as well as in removing preadsorbed mucin layers from different surfaces. On the other hand, the nonionic surfactant n-dodecyl β-D-maltopyranoside (C12-mal), does not affect significantly the mucin aggregates in solution, neither does it remove mucin effectively from a negatively charge hydrophilic surface (silica). It can be suggested that nonionic surfactants (like the sugar–based C12-mal) could be used to obtain milder oral care products. The second type of systems consisted of positively charged polyelectrolytes and a negatively charged surfactant (SDS). These systems are relevant to a wide variety of applications ranging from mining and cleaning to gene delivery therapy. It was found that the interactions of these polyelectrolytes with SDS depend strongly on the polyelectrolyte structure, charge density and the solvent composition (pH, ionic strength, and so on). Large solvent isotopic effects were found in the interaction of polyethylene imine (PEI) and SDS, as well as on the interactions of this anionic surfactant and the sugar–based n-decyl β-D-glucopyranoside (C10G1). These surfactants mixtures formed similar structures in solutions to the ones formed by some of the polyelectrolytes studied, i.e. ellipsoidal micelles at low electrolyte concentration and stiff rods, at high electrolyte and SDS concentrations.
QC 20100901

Interactions of colloidal particles with surfaces occur in natural and engineered systems, and they influence the transport of contaminants through diffusion, aggregation, filtration, and sedimentation. To quantify the transport and fate of colloidal particles and their influence on environmental systems, it is important to understand their interactions with surfaces. These interactions are influenced by physical and chemical surface properties such as hydrophobicity, charge density, and roughness, as well as environmental conditions such as relative humidity (RH). In atmospheric systems, RH induces the capillary force and also influences the contributions of van der Waals and electrostatic forces. To investigate the role of surface properties and RH in the interaction of colloidal particles with surfaces, atomic force microscopy was employed to measure the adhesion and friction forces of colloidal particles including Bacillus thuringiensis spores, silica, and gold at various experimental conditions with several types of surfaces including mica, silica, and radioactive gold. Contributions to the adhesion force by van der Waals, capillary, and electrostatic forces were theoretically calculated and compared to measured forces. Through experimental results and theoretical studies, it was identified how surface properties of interacting surfaces and experimental conditions influence the interfacial interactions of colloidal particles in atmospheric systems. The role of RH in adhesion and friction depends on the hydrophobicity or contact angles of interacting surfaces and surface roughness. Relative humidity also influences the contribution of electrostatic force to the total adhesion force by screening the strength of surface potential or providing a passage for charge leakage. The results of this thesis provide a better understanding of particulate processes that are influenced by the interactions of colloidal particles with surfaces and can be useful in monitoring and control of contamination in atmospheric systems.

Adsorption on solid surfaces from solution is a fundamental property of a surfactant. It might even be the most important aspect of surfactant behavior, since it influences many applications, such as cleaning, detergency, dispersion, separation, flotation, and lubrication. Consequently, fundamental investigations of surfactant adsorption are relevant to many areas.

The main aim of this thesis has been to elucidate the adsorption properties, primarily on the solid/water interface, of a particular class of polyhydroxyl based surfactants: the alkyl glucosides. By the use of ellipsometry, the equilibrium and kinetic aspects of adsorption on titanium dioxide with respect to structural effects has been studied. Furthermore, the effects of small amounts of cationic surfactant additives on the adsorption on silica have been investigated. The results have been compared with similar studies for other nonionic surfactants.

We have found that the surfactant structure has a strong effect on the adsorption properties. An increase in the surfactant chain length increases the cooperativity of the system. An increase in the head group polymerization decreases the cooperativity and the plateau adsorbed amount at equilibrium. The effect of surfactant structure on the adsorption kinetics depends on the concentration relative to the cmc, while the there is a decrease in the rate of desorption with increasing hydrophobic chain length independent of the concentration. The adsorption/desorption process is concluded to be diffusion driven, as suggested by the model used. When comparing these results with studies on ethylene oxide based surfactants, we conclude that the two types of surfactants exhibit similar trends on surfaces onto which they adsorb.

Adsorption from binary surfactant solutions is even more interesting than adsorption from single surfactant solutions, since it brings us one step closer to the systems used in applications. In addition, adsorption from a mixture can be very different from adsorption from any of the single surfactants in the mixture. Alkyl glucosides alone do not adsorb on silica, but addition of small amounts of a cationic surfactant to the alkyl glucoside solution allows for adsorption on silica. A comparison between the adsorption and bulk properties has shown that mixed micellization explains most, but not all, effects of the coadsorption properties. Changing the pH in the mixed systems reveals that a surfactant with a pH-dependent charge and the ability to adapt its charge to the environment, e.g. a surface, enhances the adsorbed amount over a wider range of pH values than a purely cationic surfactant.

It is well known that alkyl glucosides and ethylene oxides adsorb differently on different types of hydrophilic surfaces. As a consequence, replacing ethylene oxides with alkyl glucosides might not be all straight-forward; however, we have shown that the effect of the surface can be eliminated by the use of a cosurfactant.

Le polissage mécano-chimique (CMP pour Chemical Mechanical Polishing) consiste à appliquer une suspension colloïdale contenant des particules abrasives sur une surface solide (le substrat) au travers d’une pression exercée par un disque de polymère (le pad) en rotation. Un substrat de silice et des particules d’oxyde de cérium ont été choisis comme système de référence pour aider à la compréhension du mécanisme de polissage CMP. Des études macroscopiques ont été réalisées sur ce système afin d'étudier les effets de la concentration ou de la taille des particules abrasives, ainsi que l’influence du pH ou de la force ionique de la suspension de polissage. Le mécanisme a également été étudié à un niveau microscopique, en se concentrant sur les interactions entre le substrat et les particules abrasives. Cela a été effectué par une approche multi-instrumentale (zêtamétrie, ATR-FTIR, MET, SAXS, dosages chimiques, AFM). L’étude du polissage implique une bonne connaissance des surfaces en jeu, l'acido-basicité et l'oxydo-réduction des surfaces de CeO2 ont donc été étudiés. A partir de la compréhension acquise, des modifications des particules abrasives ont été réalisées (synthèse de particules cœur-coquilles et de solutions solides), et des particules de CeO2 de morphologies différentes testées
Chemical Mechanical Polishing (CMP) consists in applying a slurry of colloidal particles onto a solid surface called substrate, through a pressure applied with a rotating polymeric pad. A silica substrate and CeO2 particles were chosen as reference system to study the mechanism of CMP. Macroscopic studies have shown the effect of the concentration and the size of abrasive particles, as well as the importance of pH and ionic strength. The mechanism was more thoroughly studied by recirculating the slurry in fixed conditions. Surface interactions between the substrate and the particles were studied thanks to a multi-instrumental approach (zeta potential, ATR-FTIR, TEM, SAXS, chemical analysis, AFM).A good understanding of the surfaces at stake is necessary to study the mechanism of polishing. Acid-basic and redox properties of the CeO2 surface were therefore investigated. Finally, the surface chemistry of the abrasive particles were modified (synthesis of core-shell particles and solid solutions), and different ceria morphologies were tested

Hydrogen is the smallest element in the periodical table. It has been shown in several studies that hydrogen has a large influence on the corrosion and cracking behaviour of stainless steels. Hydrogen is involved in several of the most common cathode reactions during corrosion and can also cause embrittlement in many stainless steels. Some aspects of the effect of hydrogen on corrosion and hydrogen-induced stress cracking, HISC, of stainless steels were studied in this work. These aspects relate to activation of test specimens for uniform corrosion testing, modification of a test cell for dewpoint corrosion testing and the mechanism of hydrogen-induced stress cracking. The results from uniform corrosion testing of superduplex stainless steels indicated that there is a large difference between passive and activated surfaces in hydrochloric acid and in lower concentrations of sulphuric acid. Hence, initial activation of the test specimen until hydrogen evolution can have a large influence on the results. This may provide another explanation for the differences in iso-corrosion curves for superduplex stainless steels that have previously been attributed to alloying with copper and/or tungsten. In concentrated sulphuric acid, potential oscillations were observed; these oscillations activated the specimen spontaneously. Due to these potential oscillations the influence of activation was negligible in this acid. An experimental set-up was developed for testing dewpoint corrosion of stainless steels in a condensate containing 1 % hydrochloric acid. There was an existing experimental set-up that had to be modified in order to avoid azeotroping of the water and hydrogen chloride system. A separate flask with hydro chloric acid was included in the experimental set-up. The final set-up provided reasonably good agreement with field exposures in contrary to much higher corrosion rates in the original set-up. Relaxation and low temperature creep experiments have been performed with several stainless steels in this work. The aim was to understand how creep and relaxation relates to material properties and the relative ranking between the tested materials. For low temperature creep with a load generating stresses below the yield strength, as well relaxation at stress levels above and below the yield strength, the same ranking with respect to changes in mechanical properties of the steel grades was found. For low temperature creep with a load level above the yield strength, the same ranking was not obtained. This effect can most probably be explained by annihilation and generation of dislocations. During low temperature creep above the yield strength, dislocations were generated. In addition, low temperature creep experiments were performed forone superduplex stainless steel in two different product forms with differentaustenite spacing in the microstructure. The superduplex material experienced low temperature creep at a lower load level for the material with large austenite spacing compared to the one with smaller austenite spacing. Also this differenceis influenced by dislocations. In a material with small austenite spacing the dislocations have more obstacles that they can be locked up against. Studies of the fracture surfaces of hydrogen induced stress cracking, HISC, tested duplex stainless steels showed that HISC is a hydrogen-enhanced localised plasticity, HELP, mechanism. Here a mechanism that takes into account the inhomogeneous deformation of duplex stainless steels was proposed. This mechanism involves an interaction between hydrogen diffusion and plastic straining. Due to the different mechanical properties of the phases in a superduplex stainless steel, plastic straining due to low temperature creep can occur in the softer ferrite phase. A comparison between low temperature creep data showed that for the coarser grained material, HISC occurs at the load levelwhen creep starts. However, in the sample with small austenite spacing, HISC did not occur at this load level. Microhardness measurements indicated that the hydrogen level in the ferrite was not high enough to initiate cracking in the coarser material. The proposed mechanism shows that occurrence of HISC is an interaction between local plasticity and hydrogen diffusion.
QC20100618

Thesis (Ph. D.)--Civil and Environmental Engineering, Georgia Institute of Technology, 2006.
Yiacoumi, Sotira, Committee Chair ; Tsouris, Costas, Committee Co-Chair ; Pavlostathis, Spyros, Committee Member ; Tannenbaum, Rina, Committee Member ; Sherrill, David, Committee Member.