With the aim of mitigating membrane fouling, an electrocoagulation (EC) based electrokinetic membrane bioreactor (EMBR) was developed and operated with real municipal wastewater under low temperatures. Both batch tests and continuous EMBR experiments demonstrated the significant advantages in membrane fouling reduction over the conventional antifouling strategies, ushering its potential applications as an attractive hybrid MBR technology for decentralized wastewater treatment in remote cold regions. The main research observations and findings could be summarized as follows: (1). Effective membrane fouling mitigation at low temperatures was due to destruction of extracellular polymeric substances (EPS) and subsequent reduction of the biocake resistance. The transmembrane pressure (TMP) increased at a much slower rate in EMBR and the filtration resistance was about one third of the control MBR prior to chemical cleaning cycle; (2). A new membrane parameter, the specific fouling rate (SFR) was proposed, relating the fouling rate with permeate flux and temperature-dependent viscosity. Pore clogging and biocake resistances were quantified for the first time with the same membrane module and operating conditions as in regular MBR, rather than resorting to the use of batch filtration setups; (3). The floc size in EMBR did not increase as a result of the air scouring shear force and decrease in the extracellular polymeric substances (EPS); (4). When current intensity was less than 0.2 A, polarity reversal had minimal impact on electrode passivation reduction due to insignificant hydrogen yield, however, if current intensity was above 0.2 A, frequent polarity reversal (< 5 min per cycle) was detrimental to electrode passivation if no sufficient mixing was provided; (5). Viability of the microorganisms in the EMBR system was found to be dependent on duration of the current application and current density. The bacterial viability was not significantly affected when the applied current density was less than 6.2 A/m2; (6). Significant abiotic ammonification was found in electrocoagulation (EC). DO in the treated liquid was depleted within an hour, under the anaerobic condition in EC, nitrate was chemometrically reduced to ammonium following a two-step first order reaction kinetics. Aeration (DO > 2 mg/L) was shown effective in suppressing abiotic ammonification; (7). Magnetic resonance imaging (MRI) technology was used for the first time as an in-situ non-invasive imaging tool to observe membrane fouling status in an EMBR. / October 2016

Thesis in theoretical part provides an overview of oral drugs in the biopharmaceutical point of view. It describes the main difficulties of this application route and presents selected facts about new approaches to improve the bioavailability of poorly absorbable substances. These approaches, in recent years, also use nanofiber membranes. The experimental part focuses on the in vitro evaluation of diamine delivery from nanofiber membranes in vehicle buffered at pH 7.4. The tested membranes contain the active substance in three graduated concentrations (20%, 30% and 40%), and specifically differ in basic weight. To evaluate the delivery the fluxes of diamine witin the first linear section of delivery are used, the percentage of substance released within 60 minutes was used to the evaluation of releasable proportion of diamine. Determination of diamine was performed by HPLC. The release of nearly all releasable diamine amounts were always obtained in 15 minutes from the beginning of release. The release rate of the diamine from nanofiber membranes is high. Important, however, is the finding that the rate of drug release is not probably significantly dependent on the drug concentration in the nanofiber membrane, but it is significantly influenced by the basic weight of membranes. The variability...

A theoretical part of the diploma thesis describes solubility, classification of solubility and ways of influencing of solubility, and it gives a detailed summary of naproxen as the drug further used and evaluated in in vitro experiments for drug release. An experimental section is focused to in vitro release of naproxen from nanofibre membranes produced by electrospinning with regard to the possibility of the use of layering. At both layered and non-layered nanofibre membranes of three different naproxen concentrations (e.g. 5%, 15% and 30% by weight) the drug release amounts within 5 minutes were from 10 to 90 percent of total amounts. An overal percentage of naproxen released in 60 minutes was always about 100 % of the total drug loaded in the nanomembranes. The nanofibre membranes layered with the glycerol and propylene glycol were of the same profiles as with non-layered membranes.

Le comportement plastifiant de polymères purs a été bien étudié dans la littérature. Toutefois, il n'y a eu que peu d'études concernant les membranes à matrices mixtes (MMM). Dans le chapitre 2 de cette thèse, le comportement plastifiant de MMM préparés à partir de nanoparticules mésoporeuses Fe(BTC) et du polymère Matrimid® est étudié avec un gaz pur ou en mélange. Les réseaux métaux-organiques (MOF) sous forme particulaires ont présenté une relativement bonne compatibilité avec le polymère. L'incorporation de Fe(BTC) dans du Matrimid® a permis d'augmenter la perméabilité et la sélectivité des membranes. Pour de faibles pressions de 5 bars, les MMM ont une perméabilité au CO2 de 60% plus grande ainsi qu'une sélectivité de 29% plus grande à comparer à la sélectivité idéale de membranes Matrimid®. Il a été observé que la présence de particules Fe(BTC) retardait l'effet plastifiant vers de plus grandes pressions. De plus, cette pression augmente avec le taux de MOF au sein du matériau. Ce retard est attribué à la mobilité réduite des chaînes polymères dans l'entourage des particules Fe(BTC). Egalement, pour des concentrations en MOF plus élevées, les membranes présentent une sélectivité plus ou moins constante sur toute la gamme de pression étudiée. Le chapitre 3 présente ensuite la préparation et le caractère plastifiant des MMMs basées sur trois types de MOFs (MIL-53(Al) (MOF « repirant »), ZIF-8 (MOF « flexible ») and Cu3(BTC)2 (MOF « rigide »)) dispersés dans le Matrimid®. Les performances en gaz pur ou en mélange ont été étudiées en fonction de la quantité de MOF introduite. Parmi les trois systèmes MOF-MMM, les membranes avec le Cu3(BTC)2 ont présenté la plus haute sélectivité alors que les membranes avec du ZIF-8 ont montré une plus grande perméabilité. Ces améliorations sont essentiellement le fait de la structure cristalline du MOF et de son interaction avec les molécules de CO2. Le chapitre 4 décrit la préparation de membranes à base de mélange Matrimid® polyimide (PI)/polysulfone (PSF) contenant des particules de ZIF-8 pour la séparation gazeuse à haute pression. Un mélange optimisé avec un rapport PI/PSF de 3:1 a été utilisé pour une étude sur la stabilité et la performance de ces MMMs incorporant différentes concentration de ZIF-8. PI et PSF étant miscibles, une bonne compatibilité avec les particules de ZIF-8 est observée. Les MMMs PI/PSF-ZIF-8 ont démontré une amélioration significative de la perméabilité en CO2 lors de l'augmentation de la concentration en ZIF-8, ce qui a été attribué à une augmentation modérée de la capacité de sorption et à une diffusion plus rapide au travers des particules de ZIF-8. Lors des mesures en gaz purs, les membranes PI/PSF (3:1) ont présenté une plastification vers 18 bars alors que l'introduction de ZIF-8 repousse cette valeur à 25 bars. En mélange de gaz, les MMMs PI/PSF-ZIF-8 ont abouti à une suppression de la plastification comme l'a confirmé une mesure constante de la perméabilité et de la sélectivité du CH4, et cet effet est plus accentué avec l'augmentation de la concentration en ZIF-8. Les résultats en séparation des gaz avec les MMMs PI/PSF-ZIF-8 montrent une performance supérieure à celle du Matrimid® ce qui laisse augurer un élargissement du spectre d'application de ces membranes, particulièrement pour la séparation du CO2 à haute pression. Dans le chapitre 5, une nouvelle voie de préparation des MMMs via la fusion contrôlée de particules a été introduite. La modification du Matrimid® par du 1-(3-aminopropyl)-imidazole a permis d'améliorer considérablement la compatibilité avec les particules de ZIF-8. Il a ainsi été possible de préparer des MMMs contenant 30% de MOF sans perte de sélectivité. En augmentant la concentration en ZIF-8, les MMMs ont de meilleures performances dans la séparation de mélange CO2/CH4 à comparer au polymère initial. La perméabilité a augmenté de plus de 200% avec une augmentation de 65% de sélectivité pour le mélange CO2/CH4. / The plasticization behavior of pure polymers is well studied in literature. However, there are only few studies on the plasticization behavior of mixed matrix membranes. In Chapter 2 of this thesis, pure and mixed gas plasticization behavior of MMMs prepared from mesoporous Fe(BTC) nanoparticles and the polymer Matrimid® is investigated. All experiments were carried with solution casted dense membranes. Mesoporous Fe(BTC) MOF particles showed reasonably good compatibility with the polymer. Incorporation of Fe(BTC) in Matrimid® resulted in membranes with increased permeability and selectivity. At low pressures of 5 bar the MMMs showed an increase of 60 % in CO2 permeability and a corresponding increase of 29 % in ideal selectivity over pure Matrimid® membranes. It was observed that the presence of Fe(BTC) particles increases the plasticization pressure of Matrimid® based MMMs. Furthermore, this pressure increases more with increasing MOF loading. This delay in plasticization is attributed to the reduced mobility of the polymer chains in the vicinity of the Fe(BTC) particles. Also, at higher Fe(BTC) loadings, the membranes showed more or less constant selectivity over the whole pressure range investigated. Chapter 3 subsequently presented the preparation and plasticization behavior of MMMs based on three distinctively different MOFs (MIL-53(Al) (breathing MOF), ZIF-8 (flexible MOF) and Cu3(BTC)2 (rigid MOF)) dispersed in Matrimid®. The ideal and mixed gas performance of the prepared MMMs was determined and the effect of MOF structure on the plasticization behavior of MMMs was investigated. Among the three MOF-MMMs, membranes based on Cu3(BTC)2 showed highest selectivity while ZIF-8 based membranes showed highest permeability. The respective increase in performance of the MMMs is very much dependent on the MOF crystal structure and its interactions with CO2 molecules. Chapter 4 described the preparation of Matrimid® polyimide (PI)/polysulfone (PSF)-blend membranes containing ZIF-8 particles for high pressure gas separation. An optimized PI/PSF blend ratio (3:1) was used and performance and stability of PI/PSF mixed matrix membranes filled with different concentrations of ZIF-8 were investigated. PI and PSF were miscible and provided good compatibility with the ZIF-8 particles, even at high loadings. The PI/PSF-ZIF-8 MMMs showed significant enhancement in CO2 permeability with increased ZIF-8 loading, which was attributed to a moderate increase in sorption capacity and faster diffusion through the ZIF-8 particles. In pure gas measurements, pure PI/PSF blend (3:1) membranes showed a plasticization pressure of ~18 bar while the ZIF-8 MMMs showed a higher plasticization pressures of ~25 bar. Mixed gas measurements of PI/PSF-ZIF-8 MMMs showed suppression of plasticization as confirmed by a constant mixed gas CH4 permeability and a nearly constant selectivity with pressure but the effect was stronger at high ZIF-8 loadings. Gas separation results of the prepared PI/PSF-ZIF-8 MMMs show an increased commercial viability of Matrimid® based membranes and broadened their applicability, especially for high-pressure CO2 gas separations. In Chapter 5, a novel route for the preparation of mixed matrix membranes via a particle fusion approach was introduced. Surface modification of the polymer with 1-(3-aminopropyl)-imidazole led to an excellent ZIF-8-Matrimid® interfacial compatibility. It was possible to successfully prepare MMMs with MOF loadings as high as 30 wt.% without any non-selective defects. Upon increasing the ZIF-8 loading, MMMs showed significantly better performance in the separation of CO2/CH4 mixtures as compared to the native polymer. The CO2 permeability increased up to 200 % combined with a 65 % increase in CO2/CH4 selectivity, compared to the native Matrimid®. Chapter 6 finally discussed the conclusions and directions for future research based on the findings presented in this thesis.

Hydrogen sulfide is toxic by-product of many petroleum, petrochemical and mineral treatment operations. Due to the increasing stringent environment regulations, toxic H2S must be completely removed from industrial waste gases before venting to the atmosphere. The H2S decomposition reaction is a well known thermodynamically limited reaction. Alumina membrane fixed bed catalytic reactors offer the potential for improved conversions at reduced operating temperature due to product separation and catalyst activity. A theoretical and experimental work dealing with a packed bed membrane reactor is the subject of this thesis. A tubular alumina membrane reactor possessing thermal and corrosion resistance has been developed. A multicomponent permeation study indicated that the fluxes of gases could be quantitatively described as a combination of Knudsen diffusion and viscous flow through the porous alumina membrane. The catalytic decomposition of hydrogen sulfide to hydrogen and sulfur was conducted in membrane reactor incorporating a commercial porous alumina membrane in combination with catalytic function of bimetallic RuMo sulfide catalyst. The obtained results demonstrate the possibility of achieving conversion above the equilibrium conversion. The reaction rate is equal to the intrinsic rate since both internal/external mass transfer and heat transfer resistance are negligible for the size of catalyst particles considered. Results obtained with this system have shown a maximum of 2.3 times the equilibrium conversion at the operating temperature 983K, which was equivalent to the conversion at operating temperature 1200K in a conventional fixed bed reactor. The conversion enhancement was significant for the operation with high sweep to feed molar ratio. The reactor configuration of membrane reactor appeared to have an influence on its performance. Comparative experimental and simulation study showed that the cocurrent mode gave slightly higher conversion over counter-current mode. Mathematical models were developed for the reactor, based on plug flow behavior. Simulation had been performed in order to validate the model against experimental data. Reactor optimization was carried out using the validated model. The simulation results from the non-isothermal model were in reasonable agreement with the experimental data. On the other hand, the isothermal model which neglected heat effects that took place in the reactor, has leaded to over-predicted conversion. This study also illustrated that predictive simulations could be used to explore the effects of recycle operation; the optimization study showed that the alumina membrane reactor permitting retentate recycle, could achieve up to 48.6% conversion, corresponding to 6 folded of the equilibrium conversion. The simulations provide a logical methodology for experimental planning and design. To further elucidate the effect of reactor configuration, operation conditions and permeation parameters on the performance of membrane reactors, a high permselective Pt-composite MR model was developed. Comparison of alumina MR and Pt-composite MR was carried out via computer simulation. Porous membrane reactor with higher permeability but lower Permselectivity can attain comparable conversion as the composite membrane reactor with higher permselectivity but lower permeability. Ptcomposite MR was more superior to alumina MR without recycle. Retentate recycle in alumina MR is shown to outperform the Pt-composite MR. Alumina MR was therefore considered as potential candidate for industrial H2S treatment.

Prokaryotic cell division is one of the most fundamental processes in biology, but the dynamics and mechanics are far from being understood. In many bacteria, FtsZ, a tubulin homologue assembles into a ring-like structure – Z-ring at precisely the middle of the cell. This accurate site selection is dependent on the Min proteins. Min D and MinE self-organise into waves in vitro, and oscillate pole to pole in vivo. MinC is thought to couple the Min oscillations to FtsZ by direct interaction. The mechanism of inhibitory action of MinC on FtsZ assembly is not known. Critical to the understanding of regulation of FtsZ by MinC and other proteins and its probable role in force generation is the organisation, structure and the dynamics of the Z-ring. Current models of the FtsZ filament organization in the Z-ring argue between two different structures – (i) short overlapping protofilaments with lateral interactions and (ii) few long annealed protofilaments with or without lateral contacts. Our observations of the characteristics of polymerization and turnover studies using fluorescence microscopy suggest that the FtsZ filament is a continuous and irresolute bundle. The results are consistent with a structure where the turnover happens throughout, and any specialised structure resulting in a GTP cap like structure can be ruled out. We show that the turnover rates and hydrolysis rates are similar arguing for a model in which subunit leaves as soon as it hydrolyses GTP. On the basis of crystal structures, we cloned the N-terminal of FtsZ, which acts as a C-terminal end capping fragment and is able to interact with monomers. The end-capping fragment, NZ can disassemble the FtsZ polymers, without influencing the GTPase activity, offering a comparable standard for the activity of MinC. On the basis of our observations, we propose a model on how MinC can disassemble FtsZ polymers. Furthermore, our data shows that the Min CDE system is sufficient to cause spatial regulation of FtsZ provided FtsZ is dynamic. How the Z-ring takes the form of a functional helical or ring-like structure remains unclear. Extensive modelling approaches have tried to explain the ring formation and force generation. Previous studies have qualitatively shown bending of liposome membranes by FtsZ filaments. We hypothesised that the presumably intrinsically curved filaments should respond to pre-curved substrates, and the alignment should be quantifiable. This should ascertain whether or not FtsZ has intrinsic curvature and/or actively induces any force. Thus, we investigated how FtsZ filaments respond to a range of curvatures, which mimic different stages of the division process. Our results show that the FtsZ filaments possess intrinsic curvatures as well as spontaneous twist. This facilitates the formation of Z-ring by utilizing geometrical cues. Our results are in agreement with consistent helical FtsZ polymers observed in vivo by Cryo-EM or super resolution microscopy. The alignment of filaments over a range of curvature suggests that the filaments have considerable flexibility, which strongly suggests reconsidering possible mechanisms of force generation. Moreover, the developed assay constitutes a valuable platform to further study proteins involved in modifying curvature of FtsZ filaments. In summary, by reconstituting the FtsZ filament in vitro, we have elucidated the nature of FtsZ filaments. The dynamics of FtsZ filaments allows them to be inhibited by MinC, thus cooperating with the Min waves. The presence of intrinsic curvature and twist facilitates their formation into a ring necessary for the cell to carry out cytokinesis.

Hybrid membranes represent a promising alternative to the limitations of organic and inorganic materials for high productivity and selectivity gas separation membranes. In this study, the previously developed concept of emulsion-polymerized mixed matrix (EPMM) membranes was further advanced by investigating the effects of surfactant and compatibilizer on inorganic loading in poly(2,6-dimethyl-1,4-phenylene oxide) (PPO)-based EPMM membranes, in which inorganic part of the membranes originated from tetraethylorthosilicate (TEOS). The polymerization of TEOS, which consists of hydrolysis of TEOS and condensation of the hydrolyzed TEOS, was carried out as (i) one- and (ii) two-step processes. In the one-step process, the hydrolysis and condensation take place in the same environment of a weak acid provided by the aqueous solution of aluminum hydroxonitrate and sodium carbonate. In the two-step process, the hydrolysis takes place in the environment of a strong acid (solution of hydrochloric acid), whereas the condensation takes place in weak base environment obtained by adding excess of the ammonium hydroxide solution to the acidic solution of the hydrolyzed TEOS. For both one- and two-step processes, the emulsion polymerization of TEOS was carried out in two types of emulsions made of (i) pure trichloroethylene (TCE) solvent, and (ii) 10 w/v% solution of PPO in TCE, using different combinations of the compatibilizer (ethanol) and the surfactant (n-octanol). The experiments with pure TCE, which are referred to as a gravimetric powder method (GPM) allowed assessing the effect of different experimental parameters on the conversion of TEOS. The GPM tests also provided a guide for the synthesis of casting emulsions containing PPO, from which the EPMM membranes were prepared using a spin coating technique. The synthesized EPMM membranes were characterized using 29Si nuclear magnetic resonance (29Si NMR), differential scanning calorimetry (DSC), inductively coupled plasma mass spectrometry (ICP-MS), and gas permeation measurements carried out in a constant pressure (CP) system. The 29Si NMR analysis verified polymerization of TEOS in the emulsions made of pure TCE, and the PPO solution in TCE. The conversions of TEOS in the two-step process in the two types of emulsions were very close to each other. In the case of the one-step process, the conversions in the TCE emulsion were significantly greater than those in the emulsion of the PPO solution in TCE. Consequently, the conversions of TEOS in the EPMM membranes made in the two-step process were greater than those in the EPMM membranes made in the one-step process. The latter ranged between 10 - 20%, while the highest conversion in the two-step process was 74% in the presence of pure compatibilizer with no surfactant. Despite greater conversions and hence the greater inorganic loadings, the EPMM membranes prepared in the two-step process had glass transition temperatures (Tg) only slightly greater than the reference PPO membranes. In contrast, despite relatively low inorganic loadings, the EPMM membranes prepared in the one-step process had Tgs markedly greater than PPO, and showed the expected trend of an increase in Tg with the inorganic loading. These results indicate that in the case of the one-step process the polymerized TEOS was well integrated with the PPO chains and the interactions between the two phases lead to high Tgs. On the other hand, this was not the case for the EPMM membranes prepared in the two-step process, suggesting possible phase separation between the polymerized TEOS and the organic phase. The latter was confirmed by detecting no selectivity in the EPMM membranes prepared by the two-step process. In contrast, the EPMM membranes prepared in the one-step process in the presence of the compatibilizer and no surfactant showed 50% greater O2 permeability coefficient and a slightly greater O2/N2 permeability ratio compared to the reference PPO membranes.

The anisotropic mass transport issues inside a fuel cell membrane have been studied in this thesis using computer modelling. The polymer electrolyte membrane (PEM) conductivity of a PEM fuel cell (PEMFC) depends on the hydration state of the hydrophilic charged sites distributed in the pores of the membrane. Water humidification of these charged sites is crucial for sustaining the membrane conductivity and reducing concerning voltage losses of the cell. During the operation of a PEMFC, the transport of humidified inlet gases (fuel/oxidant) is influenced by external design factors such as flow field plate geometry of the gas circulating channels. As a result, there arises a distribution in the mass transport of water inside the membrane electrode assembly. A two-dimensional, cross-the-channel, fuel cell membrane layer mass transport model, developed in this work, helps the study of the impact of factors causing the distribution in the membrane ionic conductivity on ohmic losses.<p>The governing equations of the membrane mathematical model stem from the multicomponent framework of concentrated solution theory. All mass transport driving forces within the vapour and/or liquid equilibrated phases have been accounted in this research. A computational model, based on the finite control volume method, has been implemented using a line-by-line approach for solving the dependent variables of the mass transport equations in the two-dimensional membrane domain. The required boundary conditions for performing the anisotropic mass transport analysis have been obtained from a detailed agglomerate model of the cathode catalyst layer available in the literature.<p>The results obtained using boundary conditions with various flow field plate channel-land configurations revealed that the anisotropic water transport in the cathode half-cell severely affects the ohmic losses within the membrane. A partially humidified vapour equilibrated membrane simulation results show that a smaller channel-land ratio (1:1) sustains a better membrane performance compared to that with a larger one (2:1 or 4:1). Resistance calculations using the computer model revealed that ohmic losses across the membrane also depend on its physical parameters such as thickness. It was observed that the resistance offered by a thinner membrane towards vapour phase mass transport is comparatively lower than that offered by a thicker membrane. A further analysis accounting the practical aspects such as membrane swelling constraints, imposed by design limitations of a fuel cell, revealed that the membrane water content and ionic conductivity are altered with an increase in the compression constraint effects acting upon a free swelling membrane.

Anaerobic membrane bioreactors may provide a sustainable technological solution for digestion of waste activated sludge due to their capacity to achieve substantial volatile solids (VS) destruction and positive energy balances with reduced digester volumes. However, membrane integrated anaerobic systems may have limitations that are imposed by membrane fouling and a decrease in biomass activity due to possible exposure of biomass to high shear conditions. This study characterised bioprocess and membrane performance under varying conditions, identified foulant type and origin and mechanism of fouling, and developed fouling control strategies by using low cross flow velocity and pressure anaerobic membrane systems. The study employed a pilot scale anaerobic digester integrated with negative and neutral tubular membranes; pilot and bench scale control digesters supported with bench scale filtration unit parametric studies. The membranes were polyvinylidene difluoride based with an average pore size of 0.02 micron and were operated at a constant cross flow velocity of 1 ms-1 and constant trans-membrane pressure of 30 kPa. Four operating conditions consisting of different combinations of HRT and SRT were evaluated. By integrating membranes into the digesters it was possible to simultaneously enhance digestion and increase throughput of the digesters without affecting its performance. The anaerobic membrane digester showed 48-49% volatile solids destruction at 30 days SRT under conventional and higher loadings of 1.2±0.4 and 2.1±0.6 kg COD m-3day-1. This was a 100% increase in performance compared to a control digester subjected to higher loading. This result was supported by the associated specific methane generation. The control digesters operated at a relatively higher SRT showed comparable VS destruction and gas generation to the anaerobic membrane running at a similar SRT. However the extra gas generated didn’t compensate heat required to maintain larger volume of the digester. In case of anaerobic membrane digesters due to the high rate feeding, increase biogas production and co-thickening, the energy balance increased by 144 and 200% under conventional and higher loading conditions respectively. Characterization of membrane performance showed that the average sustainable flux was 23.2±0.4 and 14.8±0.4 LMH during HRT-SRTs of 15-30 and 7-15 days respectively. The critical fluxes were in the range of 30-40, 16-17 and 20-22 LM-2H-1 during HRT-SRTs of 15-30, 7-30 and 7-15 days respectively. The decline in membrane performance at a higher loading was associated with the formation of cake layers on the membrane surface that led to reversible fouling. The additional decline in performance at extended SRT was attributed to irreversible fouling. The colloidal fraction of the sludge showed an overall higher fouling propensity during the long term pilot studies and short term filtration tests. The suspended solids fraction of the sludge showed a positive impact at concentration below 15 g/L but resulted in a decrease of membrane performance at higher concentrations. Further studies of foulant origin through a series of microscopic, membrane cleaning and sludge characterization studies showed that the colloidal proteins, soluble carbohydrates and inorganic materials such as iron, calcium and sulfur and their interaction to have a significant impact on membrane fouling. To control anaerobic membrane fouling by the digested sludge, integration of membrane relaxation techniques in the filtration cycle were found effective. By incorporating a unique relaxation technique to tubular membranes, it was possible to increase the sustainable flux to 29.2±1.8 and 34.5±2.5 LM-2H-1 for neutral and negative membranes during 15-30 HRT-SRT process condition. Addition of cationic polymers and sequential mechanical-citric acid membrane cleaning, that targeted both reversible and irreversible fouling was also found effective.

The anisotropic mass transport issues inside a fuel cell membrane have been studied in this thesis using computer modelling. The polymer electrolyte membrane (PEM) conductivity of a PEM fuel cell (PEMFC) depends on the hydration state of the hydrophilic charged sites distributed in the pores of the membrane. Water humidification of these charged sites is crucial for sustaining the membrane conductivity and reducing concerning voltage losses of the cell. During the operation of a PEMFC, the transport of humidified inlet gases (fuel/oxidant) is influenced by external design factors such as flow field plate geometry of the gas circulating channels. As a result, there arises a distribution in the mass transport of water inside the membrane electrode assembly. A two-dimensional, cross-the-channel, fuel cell membrane layer mass transport model, developed in this work, helps the study of the impact of factors causing the distribution in the membrane ionic conductivity on ohmic losses.<p>The governing equations of the membrane mathematical model stem from the multicomponent framework of concentrated solution theory. All mass transport driving forces within the vapour and/or liquid equilibrated phases have been accounted in this research. A computational model, based on the finite control volume method, has been implemented using a line-by-line approach for solving the dependent variables of the mass transport equations in the two-dimensional membrane domain. The required boundary conditions for performing the anisotropic mass transport analysis have been obtained from a detailed agglomerate model of the cathode catalyst layer available in the literature.<p>The results obtained using boundary conditions with various flow field plate channel-land configurations revealed that the anisotropic water transport in the cathode half-cell severely affects the ohmic losses within the membrane. A partially humidified vapour equilibrated membrane simulation results show that a smaller channel-land ratio (1:1) sustains a better membrane performance compared to that with a larger one (2:1 or 4:1). Resistance calculations using the computer model revealed that ohmic losses across the membrane also depend on its physical parameters such as thickness. It was observed that the resistance offered by a thinner membrane towards vapour phase mass transport is comparatively lower than that offered by a thicker membrane. A further analysis accounting the practical aspects such as membrane swelling constraints, imposed by design limitations of a fuel cell, revealed that the membrane water content and ionic conductivity are altered with an increase in the compression constraint effects acting upon a free swelling membrane.