No description available.

<p>Nanofiltration (NF) is a pressure-driven membrane separation process, which is a nonequilibrium process because of the pressure difference and concentration difference across the membrane. As one type of molecular dynamics (MD) simulations, nonequilibrium molecular dynamics (NEMD) simulations can provide the dynamics properties of NF transport on a molecular level description, which can serve as a complement to conventional experimental studies.</p> <p>In this thesis, NEMD simulations are proposed to study pressure-driven liquid flows through carbon nanotube (CNT) membranes and polyamide (PA) membranes at realistic NF conditions. Pure water flows passing through the membranes are studied primarily, and organic flows passing through the CNT membranes are also studied. Little research, that we are aware of, has been done to show the NF transport properties. The results of the NEMD simulations are analyzed to investigate the transport properties and the effects of the membrane structures on liquid transport, and the simulation results are compared with traditional models and/or literature data. This work shows that show that the liquid transport through the CNT membrane is extremely fast and cannot be predicted by the continuum equations due to the special properties of the CNT, and the water transport of the PA membrane is strongly related to the free-volume properties of the amorphous polymeric membrane.</p> <p>The MD simulation studies proposed in this thesis are feasible as a tool for describing and investigating pressure-drive liquid transport and can provide some fundamental basis for NF transport.</p> / Doctor of Philosophy (PhD)

Supported Ni and Rh catalysts were developed for the reforming of two greenhouse gases, methane and carbon dioxide to syngas (a mixture of hydrogen and carbon monoxide). This is an endothermic, equilibrium limited reaction. To overcome the thermodynamic limitations, a commercially available porous membrane (Vycor glass) was used in a combined reactor-separator configuration. This was to selectively remove one or more of the products from the reaction chamber, and consequently shift the equilibrium to the right. However, the separation mechanism in this membrane involved Knudsen diffusion, which provided only partial separations. Consequently, there was some transport of reactants across the membrane and this led to only marginal improvements in performance. To overcome this limitation, a new membrane was developed by modifying the Vycor substrate by the chemical vapor deposition of a silica precursor. This new membrane, termed Nanosil, provided high selectivity to hydrogen at permeabilities comparable to the support material. Application of this membrane in the combined reactor-separator unit provided higher conversions than that obtained using the Vycor membrane. / Ph. D.

Hair cell structures are one of the most common forms of sensing elements found in nature. In humans, approximately 16,000 auditory hair cells can be found in the cochlea of the ear. Each hair cell contains a stereocilia, which is the primary structure for sound transduction. This study looks to develop and characterize a bilayer lipid membrane (BLM) operated artificial hair cell sensor that resembles the stereocilia of the human ear. To develop this sensor, a flexible substrate with internal compartments for hosting the biomolecules and mating cap are constructed and experimentally characterized. The regulated attachment method (RAM) is used to form bilayers within the sealed device. Capacitance measurements of the encapsulated bilayer show that the sealing cap slightly compresses the bottom insert and reduces the size of the enclosed bilayer. Single channel measurements of alamethicin peptides further verify that the encapsulated device can be used to detect the gating activity of transmembrane proteins in the membrane. The flexible substrate was incorporated into a low-noise, portable test fixture. The response of the sensor and tip velocity of the hair were measured with respect to an impulse input on the test fixture and several frequency response functions (FRFs) were created. The FRF between the sensor and the tip velocity was used to show that the hair vibration was transmitted to the bilayer for certain hair lengths. The transfer function between the sensor and the input was used to show the effect of membrane potential on sensor response. / Master of Science

The interplay between lipids and membrane proteins is known to affect membrane protein topology and thus have significant effect (control) on their functions. In this PhD thesis, the influence of lipids on the membrane protein function was studied using three different membrane protein models. A monotopic membrane protein, monoglucosyldiacylglyecerol synthase (MGS) from Acholeplasma laidlawii is known to induce intracellular vesicles when expressed in Escherichia coli. The mechanism leading to this unusual phenomenon was investigated by various biochemical and biophysical techniques. The results indicated a doubling of lipid synthesis in the cell, which was triggered by the selective binding of MGS to anionic lipids. Multivariate data analysis revealed a good correlation with MGS production. Furthermore, preferential anionic lipid sequestering by MGS was shown to induce a different fatty acid modeling of E. coli membranes. The roles of specific lipid binding and the probable mechanism leading to intracellular vesicle formation were also investigated. As a second model, a MGS homolog from Synechocystis sp. PCC6803 was selected. MgdA is an integral membrane protein with multiple transmembrane helices and a unique membrane topology. The influence of different type of lipids on MgdA activity was tested with different membrane fractions of Synechocystis. Results indicated a very distinct profile compared to Acholeplasma laidlawii MGS. SQDG, an anionic lipid was found to be the species of the membrane that increased the MgdA activity 7-fold whereas two other lipids (PG and PE) had only minor effects on MgdA. Additionally, a working model of MgdA for the biosynthesis and flow of sugar lipids between Synechocystis membranes was proposed. The last model system was another integral membrane protein with a distinct structure but also a different function. The envelope stress sensor, CpxA and its interaction with E. coli membranes were studied. CpxA autophosphorylation activity was found to be positively regulated by phosphatidylethanolamine and negatively by anionic lipids. In contrast, phosphorylation of CpxR by CpxA revealed to be increased with PG but inhibited by CL. Non-bilayer lipids had a negative impact on CpxA phosphotransfer activity. Taken together, these studies provide a better understanding of the significance of the interplay of lipids and model membrane proteins discussed here.

Membrane processes can cover a wide range of separation problems [with a specific membrane (membrane structure) required for every problem]. Thus, there are membranes available that differ in their structure and consequently in the functionality. Therefore membrane characterization is necessary to ascertain, which membrane may be used for a certain separation. Membranes of pore size ranging from 100nm to 1μm with a uniform pore size are very important in membrane technology. An optimum performance is achieved when the membrane is as thin as possible having a uniform pore size. Here in this thesis, membranes were synthesized by particle assisted wetting using mono-layers of silica colloids as templates for pores along with polymerizable organic liquids on water surface. The pore size reflects the original shape of the particles. Thus it is possible to tune the pore size by varying the particle size. This method is effective to control pore sizes of membranes by choosing silica particles of suitable size. This approach gives a porous structure that is very thin, but unfortunately limited in mechanical stability. Thus there is a need for support which is robust and can withstand the various mechanical stresses. A small change in the membrane or defect in the layered structure during the membrane formation can have drastic effect on the assembly. Lateral homogeneity of the layer generated by the particle assisted wetting can be judged by examination of its reflectivity, but once it is transferred on any solid support this option is no more. So a method is needed to detect the cracks or the inhomogenity of the membrane which can be detected even after the transfer. To tackle this problem a very simple and novel technique for characterizing the membrane by fluorescence labeling and optical inspection was developed in this thesis. The idea was to add a fluorescent dye which is poorly water soluble to the spreading solution comprising of the particles and the monomer. If the dye survived the photo-cross linking, then it would be embedded in the cross-linked polymer and would serve as a marker. Defects and inhomogenity would show up as cracks and spots. By the method that we have developed, we can detect our membrane from the support and spot defects.

Separation of dissolved metals from aqueous solutions using liquid membrane technology is highly advantageous owing to the degree of separation achieved, efficiency and application potential. In the present investigation four types of liquid membranes - bulk liquid membrane (BLM), emulsion liquid membrane (ELM), electrostatic pseudo liquid membrane (ESPLIM) and unified liquid membrane (ULM) have been extensively studied, for their application in extraction and concentration of dissolved metals from effluents. Experiments were conducted with various metal systems to optimize both system and process conditions and to find out the effect of various parameters on the performance of the process. Different mass transport models were proposed for each type, taking diffusional and kinetic resistances into account. Models were extended for simultaneous extraction systems and were verified by different metal-carrier experiments. Good agreement was found between the concentration profiles obtained from the models and the experimental data, thereby establishing the validity of models for all the four types of liquid membranes. The stirred cell employed in BLM process eliminates emulsification and demulsification processes. It also provides simultaneous contact of the organic liquid membrane phase with aqueous feed and strip phases. Overall rate expressions for extraction and stripping in BLM are based on an assumed kinetic mechanism to explain the process qualitatively. It was found that the magnitude^ of diffusional and kinetic resistances determines the overall mass transfer coefficient. The relative magnitude of mass transfer coefficient, reaction rate constants and equilibrium constants enables to visualize the controlling regime of the process. The problem of low flux rate due to high diffusion resistances, inefficient operation and exorbitant costs encountered in bulk and supported liquid membranes (SLM) are overcome in an ELM. In the ELM process, an emulsion of organic membrane phase and aqueous inner phase, is dispersed in the continuous aqueous feed phase. This gives a highly selective and ultra thin liquid film generating a large mass transfer area for separation. Experimental results on membrane instability and emulsion swelling indicate that volumetric leakage rate depends linearly on the stirring speed and that the nature of surfactant does not have any appreciable effect on emulsion swelling. A general permeation model was developed taking into account the external mass transfer around the emulsion drop, diffusion in the drop, reaction at the aqueous-organic interface, leakage of the internal phase to the external phase due to membrane breakup and emulsion swelling due to osmotic pressure difference. Model equations with appropriate boundary conditions were numerically solved by orthogonal collocation technique for a set of model parameters obtained either from known correlations or from independent experiments. Comparison of the model predictions with experimental data from the batch permeation of chromium and other metals using carrier Alamine 336 or LIX 64N, shows that the model predictions are in very good agreement with the experimental findings. Further this model can be used to simulate the effects of various experimental conditions such as metal and hydrogen ion concentrations, carrier concentration, drop diameters, etc., for similar systems. Studies on ESPLIM were conducted with the aim of demonstrating the effectiveness of this new separation process and to develop a simple transport model for metal permeation. In the ESPLIM process, a high electrical field (3-5 kV A.C.) is used for phase dispersion. This system consists of a rectangular reactor filled with membrane solution divided into extraction and stripping cells by a centrally placed integrated type baffle which also acts as an electrode. Two more electrodes were placed in the extraction and stripping cells, where feed and strip phases are introduced from the top of the reactor. When high electrical field is applied across the electrodes, fine droplets of feed and strip are formed and are dispersed in extraction and stripping cells where simultaneous extraction and stripping occurs. The process can be viewed as simultaneous counter current extraction and stripping. The aqueous drops coalesce in the settlers at the bottom of the reactor and are removed continuously. Steady state mass transport model proposed for ESPLIM system accounts for the vertical counter-current extraction and stripping processes taking place in the extraction and stripping cells, together with the lateral transport process of the metal-complex and carrier across the two cells through the integrated baffle zone. The model equations were solved analytically to obtain concentration profiles as a function of the height of the reactor. The required parameters such as mass transfer coefficients, diffusion coefficients etc. were estimated using different correlations. Model predictions agreed remarkably well with the experimental data under various process conditions. From this investigation, it was found that ESPLIM is a simple, efficient and economical process and can be applied in a variety of situations. Based on a suitable combination of solvent extraction, dispersion and liquid membrane technique, a new type of separation system called " Unified Liquid Membrane " was developed. The ULM unit was designed and fabricated, and experiments were conducted to evaluate its performance. The ULM is basically derived from ESPLIM by changing the reactor, baffle design and dispersion technique. Aqueous feed and strip phases were atomized using compressed air through a fine nozzle and are dispersed on either side of an integrated baffle plate that divides the reactor into extraction and stripping cells. Tapering bottom of the reactor reduces the dead volume of the liquid in the settlers and the baffle plate remarkably reduces the leakage problem as well as the resistance through the baffle. Experiments were conducted using LIX 64N and Alamine 336 as carriers for copper and chromium and / or zinc. Mass transport model proposed considers both chemical and phase equilibria in extraction and stripping cells, vertical and lateral transport of carrier and complex across the extraction and stripping cells through the baffle zone. The model equations were solved using initial conditions at the top of the reactor, and equilibrium data for extraction and stripping cells. Effect of various experimental conditions and process parameters was simulated using this model and the model predictions are found to be in excellent agreement with the experimental data. The ULM system developed in this investigation overcomes the major limitations encountered with the other types of liquid membranes while retaining all the advantages of this technology. The problem of high mass transfer resistance from bulk phase to metal permeation as in the case of BLM was eliminated by good phase dispersion. Additional resistance to mass transport from solid membrane as in the case of SLM was removed by using an integrated baffle which also avoids problems of membrane instability, pore clogging and selectivity. The complex problems of emulsification and demulsification were completely eliminated making the system much simpler and efficient. Very good phase dispersion was obtained by atomization without the need for either stirring the whole system or application of high electrical field in the reactor. The membrane liquid within the integrated baffle elements allows easy transport of different species between extraction and stripping cells while completely preventing the mixing of the two aqueous phases. The problems of leakage, swelling and occlusion were avoided due to very short residence time of the aqueous drops in the reactor. It was found that the new ULM configuration is simple, elegant, highly efficient and superior to the other types of liquid membrane systems.

No description available.

Les eaux usées peuvent possiblement être traitées par un système membrane intégré et combinant les procédés de bioréacteur à membrane (BAM) et d’osmose inverse (OI) pour une élimination efficace des micropolluants en vue de la réutilisation des eaux. Cependant, le rejet des concentrats d’OI dans l’environnement pourraient représenter un danger en raison de la toxicité de certains de leurs composés (micropolluants, sels, matières organiques). Une des solutions possibles peut être de recycler le concentrat d’OI vers le BAM. Néanmoins, une étude approfondie s’impose pour une telle configuration car le recyclage mettrait en jeu la recirculation de matière organique non biodégradable, ou de fortes concentrations en sels ou micropolluants, qui pourraient finalement engendrer, directement ou indirectement, un colmatage de la membrane ainsi qu’une modification de l’activité bactérienne dans le BAM. Les effets du recyclage de concentrat d’OI sur les performances de BAM ont été étudiés de deux différentes manières, en distinguant les effets à court-terme (ou court temps de contact) et les effets à long-terme (ou long temps de contact). Les résultats montrent qu’après un temps de contact de 3 heures entre le concentrat et les boues, les concentrations en protéines et polysaccharides dans le surnageant restent inchangées par rapport au début de l’opération. Une analyse HPLC-SEC a permis d’étudier les effets du concentrat d’OI sur la production de matières microbiennes solubles de types protéique. Un pic de concentration en substances protéiques ayant une masse moléculaire de 10 à 100 kDa a été observé dans le surnageant juste après l’addition du concentrat d’OI. Le pouvoir colmatant des boues n’a lui pas été modifié après l’injection du concentrat d’OI. Cette observation ouvre sur la possibilité de développer une opération d’OI comme traitement tertiaire en aval du BAM. La combinaison BAM-OI pourrait donc être une solution envisageable pour traiter le concentrat d’OI. Pour les longs temps de contact, les résultats ont montré que l’impact de l’effluent toxique (concentrat d’OI) sur les boues dépendait du rendement de l’opération d’OI et des caractéristiques du concentrat. Les mêmes tendances ont été observées quelle que soit la composition du concentrat en sels et en matière organique, puisqu’une augmentation de la concentration en protéine a été mise en évidence. L’effet du recyclage du concentrat d’OI a aussi été étudié à différents débits et avec différentes caractéristiques. Les effets sur les performances globales du BAM ainsi que sur son colmatage ont plus particulièrement été investigués. Le taux d’abattement en termes de Demande Chimique en Oxygène (DCO) est, dans tous les cas, supérieur à 93 %, quel que soit le débit de recyclage. Des résultats similaires ont été obtenus en termes de Carbone Organique Dissous. De plus, l’efficacité de la nitrification n’a pas été affectée en présence de concentrat d’OI dans le BAM. L’analyse HPLC-SEC a révélé un pic important de concentration en composés protéiques dans le surnageant, avec des masses moléculaires comprises entre 10 et 100 kDa et entre 100 et 1000 kDa. Par conséquent, une augmentation significative du pouvoir colmatant des boues a été observée et attribuée à la présence de protéines. Par ailleurs, le recyclage du concentrait d’OI n’a pas eu d’effet sur l’élimination de la carbamazépine et du diclofenac dans le BAM. Au contraire, l’élimination du ketoprofene a légèrement baissé, en passant de 94 à 72 %. Enfin, l’effet du recyclage de concentrat d’OI sur la biodégradation a été révélé comme insignifiant, ce qui indique que le recyclage du concentrat d’OI pourrait être une bonne alternative pour réduire les concentrats d’OI et limiter leur rejet dans l’environnement. / Wastewater effluents can be treated by an integrated membrane system combining membrane bioreactors (MBR) and reverse osmosis (RO) for effective removal of micropollutants in the field of high-quality water reuse. However, discharging the RO concentrate waste stream directly into the natural environment could lead to serious problems due to the toxic components contained in the concentrates (micropollutants, salts, organic matter). A possible solution could be the recirculation of RO concentrate waste to the MBR. However, such an operation should be studied in detail since the recirculation of non-biodegradable organic matter or high concentrations of salts and micropollutants could directly or indirectly contribute to MBR membrane fouling and modification of the biodegradation activity. The effects of RO concentrate recirculation on the MBR performances were investigated in two different ways of contact, i.e. short term peak contact and long-term continuous contact at various operating conditions. The results demonstrated that after 3 hours of contact time between the sludge and concentrate, the same values of both protein and polysaccharide concentrations were found in the supernatant, compared to that at the beginning of the reactor. HPLC-SEC analysis was employed to study the effects of RO concentrate on the production of protein-like SMPs. A significant peak of protein-like substances with a molecular size of 10-100 kDa was observed immediately in the supernatant after the addition of RO concentrate. Besides, no significant change was found of the sludge fouling propensity after the injection of RO concentrate into the activated sludge. This finding proposes the opportunities to develop RO process as a tertiary treatment of the membrane bioreactor (MBR), hence, the integrated MBR - RO concept with the RO concentrate recirculation to the MBR might be a solution to treat the concentrate waste stream produced by RO. During the long-term continuous contact, the results demonstrated that the impact of the toxic flow on activated sludge depends on the recovery of the RO step and the characteristics of the concentrate but the same trends were observed whatever the organic matter and salt contents of the concentrates: the concentration of proteins increased. The effects of the reverse osmosis concentrate recirculation, at different flow rates and with different characteristics, to the MBR were investigated. Their impacts on MBR global performances, especially the MBR fouling were evaluated. The removal efficiencies of chemical oxygen demand (COD) at the different flow rates of concentrate were greater than 93%. Similar results for the dissolved organic carbon removal efficiency were found in the MBR. Additionally, the presence of RO concentrate in the MBR did not inhibit the nitrification process. HPLC-SEC analysis employed to study the effects of RO concentrate on the production of protein-like SMPs demonstrated a significant peak of protein-like substances corresponding to 10-100 kDa and 100-1000 kDa molecules in the supernatant. Thus a significant increase of sludge fouling propensity was observed, which could be attributed to the increased quantity of protein-like substances. Furthermore, the recirculation of RO concentrate to the MBR did not significantly affect the removal of carbamazepine and diclofenac in the MBR. Meanwhile, the removal rate of ketoprofen was impacted slightly by the RO concentrate recycling to the MBR (from 94 to 72%). Finally, the effect of the concentrate on sludge activity was studied and no significant effect was observed on biodegradation, indicating that the return of the concentrate to the MBR could be a good alternative for the reduction of concentrate quantities before disposal to the environment.

Zeolite membranes are formed as a thin zeolitic layer on the supports. They are usually synthesized by hydrothermal methods in batch systems. In this study, MFI and SAPO-34 type zeolite membranes were produced on macroporous tubular alumina supports in a recirculating flow system at elevated temperatures for the first time in the literature. During the synthesis, the synthesis mixture is flown between the reservoir and the membrane module which includes the support material. The synthesis temperatures were 180&deg / C and 220&deg / C, and the corresponding system pressures were approximately 20 and 30 bars for MFI and SAPO-34, respectively. The CH4 and n-C4H10 single gas permeances were measured through MFI membranes and the performance of membranes was investigated in the separation of equimolar CH4/n-C4H10 mixtures. The best MFI membrane had a CH4 single gas permeance of 1.45x10-6 mol/m2-s-Pa and CH4/n-C4H10 ideal selectivity of 35 at 25oC. The membranes preferentially permeated n-C4H10 in the separation of mixtures. The n-C4H10/CH4 separation selectivity was 43.6 with a total permeance of approximately 0.8x10-6 mol/m2-s-Pa at 25oC. The ideal selectivities of CO2/CH4 of SAPO-34 membrane synthesized in stagnant medium were 227, and &gt / 1000 at 220 and 200oC, respectively. Formation of amorphous structure and the additional secondary phases (impurities) were observed on SAPO-34 membranes synthesized in recirculating flow system. The results showed that it is possible to produce SAPO-34 and high quality MFI membranes by a recirculating flow system operating at elevated temperature.