This dissertation addresses the role of individual fouling mechanisms on productivity decline and solute mass transport in nanofiltration (NF) of surface waters. Fouling mechanisms as well as solute mass transport mechanisms and capabilities must be understood if NF of surface waters is to be successful. Nanofiltration of surface waters was evaluated at pilot-scale in conjunction with advanced pretreatment processes selected for minimization of nanofilter fouling, which constituted several integrated membrane systems (IMSs). Membrane fouling mechanisms of concern were precipitation, adsorption, particle plugging, and attached biological growth. Fouling was addressed by addition of acid and antiscalent for control of precipitation, addition of monochloramine for control of biological growth, microfiltration (MF) or coagulation-sedimentation-filtration (CSF) for control of particle plugging, and in-line coagulation-microfiltration (C/MF) or CSF for control of organic adsorption. Surface water solutes of concern included organic solutes, pathogens, and taste and odor compounds. Solute mass transport was addressed by evaluation of total organic carbon (TOC), Bacillus subtilis endospores, gesomin (G), 2-methlyisoborneol (MIB), and threshold odor number (TON). This evaluation included modeling to determine the role of diffusion in solute mass transport including assessment of the homogeneous solution diffusion equation. A cellulose acetate (CA) NF was less susceptible to fouling than two polyamide (PA) NFs. NF fouling was minimized by the addition of monochloramine, lower flux, lower recovery, and with the use of a coagulant-based pretreatment (C/MF or CSF). NF surface characterization showed that the low fouling CA film was less rough and less negatively charged than the PA films. Thus the theory that a more negatively charged surface would incur less adsorptive fouling, due to charge repulsion, was not observed for these tests. The rougher surface of the PA films may have increased the number of sites for adsorption and offset the charge repulsion benefits of the negatively charged surface. The addition of monochloramine significantly reduced biodegradation and integrity loss of the CA membrane. PA membranes are inherently not biologically degradable due to their chemical structure. Monochloramination reduced the rate of fouling of the PA membrane but resulted in a gradual increase in water mass transfer coefficient and a decrease in TDS rejection over time, which indicated damage and loss of integrity of the PA membrane. Based on surface characterization by X-ray Photoelectron Spectroscopy (XPS) and Fourier Transform Infrared Spectrometry (FTIR), the PA membrane degradation appeared to be chemically-based and initiated with chlorination of amide nitrogen and/or aromatic rings, which ultimately resulted in disruption of membrane chemical structures. The recommended Integrated Membrane System to control fouling of a surface water nanofiltration system is CSF monochloramine/acid/antiscalent„³monochloramine-tolerant NF. This IMS, at low flux and recovery, operated with no discernable fouling and is comparable to a groundwater nanofiltration plant with cleaning frequencies of once per six months or longer. A significant portion of the organic solutes including total organic carbon (TOC) passing through the membranes was diffusion controlled. Permeate concentration increased with increasing recovery and with decreasing flux for both PA and CA membranes. The influence was diminished for the PA membrane, due to its high rejection capabilities. Total rejection of spores used as pathogen surrogates was not achieved as spores were indigenous and high spore concentrations were used in all challenge studies; however, Integrated Membrane System spore rejection exceeded credited regulatory rejection of similar sized microorganisms by conventional treatment by several logs. Spore rejection varied by NF but only slightly by MF as size-exclusion controlled. There was no difference among spore rejection of IMS with and without in-line coagulation. Consequently, these results indicate membrane configuration (Hollow fiber>Spiral Wound) and membrane film (Composite Thin Film>CA) significantly affected spore rejection. Geosmin and methylisoborneol have molecular weights of 182 and 168 respectively, and are byproducts of algal blooms, which commonly increase taste and odor as measured by the threshold odor number (TON) in drinking water. Although these molecules are neutral and were thought to pass through NFs, challenge testing of IMS unit operations found that significant removal of TON, G and MIB was achieved by membrane processes, which was far superior to conventional processes. A CA NF consistently removed 35 to 50 percent of TON, MIB, and G, but did not achieve compliance with the TON standard of 3 units. A PA NF provided over 99 percent removal of MIB and G. Challenge tests using MIB and G indicated that size-exclusion controlled mass transfer of these compounds in NF membranes.

The research reported herein describes the study activities performed by University of Central Florida (UCF) on behalf of the Town of Jupiter Water Utilities (Town). The Town recently changed its water treatment operations from a combination of reverse osmosis (RO), lime softening (LS) and anion-exchange (IX) to a combination of RO, IX and nanofiltration (NF). Although this treatment change provided enhanced water to the surrounding community in terms of better contaminant removal and reduced DBP formation potential, integration of the NF process altered finished water quality parameters including pH, alkalinity and hardness. There was concern that these changes could result in secondary impacts related to accelerated corrosion of distribution system components and subsequent regulatory compliance. In addition, replacement of the LS process altered the in-plant blending operations by creating an unstable intermediate blend composed of RO and IX waters. There were concerns that this intermediate blend was affecting the integrity of in-plant hydraulic conveyance components. UCF developed a corrosion monitoring study to assess the potential impacts related to internal corrosion, water quality and regulatory compliance after integrating NF into the existing water supply. The intended purpose was to further highlight the complexities of corrosion, describe a unique approach to corrosion monitoring as well as offer various recommendations for corrosion control in a system that relies on a blended water supply. Research was conducted in three phases to address the in-plant and distribution system corrosion issues separately and identify appropriate corrosion control treatment alternatives. The three test phases included: a baseline conditions assessment to iv compare corrosion of the intermediate RO-IX blend with the finished water blend (ROIX-NF); an in-plant corrosion control evaluation; and a distribution system corrosion control evaluation. A test apparatus was constructed and operated at the Town’s facilities to monitor corrosion activity of mild steel, copper and lead solder metal components. The test apparatus consisted of looped PVC pipe segments housed with electrochemical probes and metal coupons to monitor corrosion rates of the metallic components. Electrochemical probes containing metal electrodes were used to obtain instantaneous corrosion rates by means of the Linear Polarization Resistance (LPR) technique while the metal coupons were gravimetrically evaluated for weight loss. The electrochemical probes permitted daily monitoring of each metal’s corrosion rates while metal coupons were analyzed at the conclusion of testing and used for comparison. Different test waters flowed through the corrosion rack according to each test phase and relative corrosion rates were compared to evaluate corrosion control techniques. Study findings indicated that the intermediate blend was more corrosive, in general, then the final blend; however, research also indicated that the final blend of water was increasing lead and copper concentrations within the distribution system. An orthophosphate corrosion inhibitor was evaluated for in-plant corrosion control. The inhibitor’s performance was assessed by comparing mild steel corrosion rates with and without the chemical. In addition, secondary impacts related to introduction of the chemical were evaluated by pre-corroding the metallic components prior to the introduction of the inhibitor. Results indicated that the inhibitor marginally decreased corrosion rates and increased the turbidity of the water supply. Based on these v observations, it was concluded that the inhibitor was not a viable solution for in-plant corrosion control. To resolve in-plant corrosion issues, recommendations were made for modification of in-plant blending operations to eliminate the corrosive intermediate blend from the process allowing the RO, IX and NF treated waters to be blended in a common location. The effectiveness of a poly/ortho blended phosphate chemical inhibitor was evaluated for reducing lead and copper corrosion to resolve distribution corrosion issues. A 50/50 poly/ortho blend was selected because of its analogous use in similar municipal water facilities. Metallic corrosion rates, particularly lead and copper, were compared with and without the inhibitor to assess the performance of the chemical. Like the previous test phase, the metallic components were pre-corroded prior to the chemical’s introduction to determine if secondary impacts could result from its presence. Results indicated that lead and copper corrosion rates were lower in the presence of the inhibitor, and secondary impacts related to increased turbidity were not observed for this chemical. Based on these results, it was recommended that a poly/ortho blended phosphate be used to decrease lead and copper corrosion within the Town’s distribution system.

The research presented in this dissertation provides the results of a comprehensive assessment of the water treatment requirements for the City of Sarasota. The City’s drinking water supply originates from two sources: (1) brackish groundwater from the Downtown well field, and (2) Floridan surficial groundwater from the City’s Verna well field. At the time the study was initiated, the City treated the brackish water supply using a reverse osmosis process that relied on sulfuric acid for pH adjustment as a pretreatment method. The Verna supply was aerated at the well field before transfer to the City’s water treatment facility, either for softening using an ion exchange process, or for final blending before supply. For the first phase of the study to evaluate whether the City can operate its brackish groundwater RO process without acid pretreatment, a three-step approach was undertaken that involved: (1) pilot testing the plan to reduce the dependence on acid, (2) implementing the plan on the fullscale system with conservative pH increments, and (3) continuous screening for scale formation potential by means of a “canary” monitoring device. Implementation of the study was successful and the annual savings in operating expenditure to the City is projected to be about $120,000. From the acid elimination study, using the relationship between electrical conductivity in water and total dissolved solids in water samples tested, a dynamic approach to evaluate the performance of the reverse osmosis plant was developed. This trending approach uses the mass transfer coefficient principles of the Homogeneous Solution Diffusion Model. Empirical models iv were also developed to predict mass transfer coefficients for solutes in terms of total dissolved solids and sodium. In the second phase of the study, the use of nanofiltration technology to treat aerated Verna well field water was investigated. The goal was to replace the City’s existing ion exchange process for the removal of hardness and total dissolved solids. Different pretreatment options were evaluated for the nanofiltration pilot to remove colloidal sulfur formed during pre-aeration of the groundwater. Sandfilters and ultrafiltration technology were evaluated as pretreatment. The sandfilter was inadequate as a pre-screen to the nanofiltration pilot. The ultrafiltration pilot (with and without a sandfilter as a pre-screen) proved to be an adequate pretreatment to remove particulates and colloids, especially the sulfur colloids in the surficial groundwater source. The nanofiltration pilot, was shown to be an efficient softening process for the Verna well field water, but it was impacted by biofoulants like algae. The algae growth was downstream of the ultrafiltration process, and so chlorination was used in the feed stream of the ultrafiltration process with dechlorination in the nanofiltration feed stream using excess bisulfite to achieve stable operations. Non-phosphonate based scale inhibitors were also used to reduce the availability of nutrients for biofilm growth on the nanofiltration membranes. The combined ultrafiltration-nanofiltration option for treatment of the highly fouling Verna water samples is feasible with chlorination (to control biofouling) and subsequent dechlorination. Alternatively, the study has shown that the City can also more economically and more reliably use ultrafiltration technology to filter all water from its Verna well field and use its current ion exchange process for removal of excess hardness in the water that it supplies

A host of environmental issues will define the state of the environment in the 21st century, with plastic pollution and water shortages among them. While solutions to these problems require large-scale, multipronged solutions, one way we can address them is through material innovation and the use of nanoparticles. In the first project, we address the issue of plastic pollution by creating nanocomposites of biodegradable polymers (PLA and PCL) with cellulose nanofibrils. Here, PLA and PCL are grafted from the surface of cellulose nanofibrils via ring-opening polymerization of cyclic ester monomers. Polymer-grafted cellulose (PGC) is characterized with structural analysis, solubility tests, thermal properties. Graft-polymer and generated free polymer are compared to evaluate assumptions about polymerization kinetics. Lastly, environmental fate of PGC is evaluated via aerobic, anaerobic, and enzymatic biodegradation tests. In the second project, we address the issue of fresh water shortage by creating screen-printed composites of polymerizable, surfactant-templated single-wall carbon nanotubes (SWNTs). Surfactant-templated SWNTs behave as lyotropic liquid crystals (LLCs), allowing self-assembly and shear-directed alignment. Here, LLC-SWNT inks are screen-printed in micron-sized channels and polymerized with UV light. Mesophase and alignment are evaluated using SAXS. Certain methods of screen printing with a stencil are found to enhance alignment and ordering of LLC-SWNTs, allowing for enhanced desalination and ion rejection.

Biogas is becoming a more important source of green, renewable energy however, its production results in a liquid wastewater, known as centrate, which must be treated due to its high levels of total dissolved solids (TDS), and chemical oxygen demand (COD). Currently, biogas generation facilities treat centrate using a combination of biological and physical treatments (via a membrane bioreactor (MBR)), which produces a stream known as MBR permeate. While MBR permeate achieves improved quality, MBR usage has several challenges including difficulty of scaling biological processes, and handling capacity limitations. In this study, membrane only treatment of centrate, collected from an operating biogas generation facility, was investigated to determine if similar quality permeates could be obtained without any biological treatments. Single- stage treatment of centrate using either polymeric or ceramic nanofiltration membranes with molecular weight cut offs between 400 and 800 Da, produced a permeate similar to MBR permeate. These membrane types caused average COD rejections of 92% and 90% respectively. However, the permeates from the nanofiltration membranes had very high levels of ammonia, which was not present in the MBR permeate. The ceramic nanofiltration membranes can achieve higher permeate fluxes than the polymeric nanofiltration membranes. Both membrane types experienced significant fouling which was removed using cleaning procedures. Two-stage treatment of centrate using ceramic nanofiltration membranes followed by polymeric reverse osmosis membranes further improved the quality of permeate and achieved COD rejections of 99% overall. While the reverse osmosis membranes did remove some ammonia, the levels were still higher than what was seen in the MBR permeate. The two-stage treatment of centrate can provide the permeate which is closest to the MBR permeate however, further studies are required to address the higher ammonia concentration values. The research shows that only using membranes is a potential treatment pathway for real centrate samples. / Thesis / Master of Applied Science (MASc) / The production of biogas, which is a green, renewable energy source results in a liquid wastewater known as centrate. This wastewater is very dirty and complex and requires treatment as it cannot be dumped and disposed of in its current state. Current treatment methods for centrate use combinations of biological treatment and filtration processes, which has its own challenges due to the complexity of biological treatments. An alternative treatment method for the centrate is nanofiltration membranes which offer the ability to treat large volumes of centrate wastewater without the complexity of relying on biological treatment options. Four different nanofiltration membranes, including two polymeric and two ceramic membranes, were used to treat real industrial wastewater samples of centrate collected from a biogas generation facility. Both types of nanofiltration membranes provided similar quality permeate to the current treatment method of centrate, which uses a combination of biological and physical treatment methods.

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<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)

Le soya est une culture en pleine expansion au Canada. L’augmentation de la production au cours des dernières années a créé un besoin au niveau du développement des compétences pour la transformation et la valorisation de cette légumineuse. L’industrie des aliments fonctionnels et des nutraceutiques s’est beaucoup intéressée au soya étant donné son contenu riche en molécules potentiellement bioactives, telles que les protéines. Cependant, il faut réussir à isoler ou concentrer ces molécules bioactives pour les rendre efficaces. Les procédés membranaires sont des technologies offrant la possibilité de fractionner des solutions afin d’en concentrer des molécules cibles. Ces technologies membranaires peuvent se diviser en deux grands groupes : celles dont la force motrice principale est la pression; dont font partie l’ultrafiltration (UF) et la nanofiltration (NF), et celles dont la force motrice est le champ électrique; l’électrodialyse avec membrane d’ultrafiltration (EDUF). Cependant, l’application de ces procédés de séparation membranaires à des solutions protéiques s’est parfois révélée problématique dû à la tendance au colmatage des membranes. Cette étude avait donc pour objectifs 1) d’évaluer le potentiel à l’encrassement des membranes échangeuses d’ions par un hydrolysat de protéines de soya, 2) de comparer l’efficacité de séparation des couplages d’UF/NF et UF/EDUF en termes de transfert de masse et de taux de migration, 3) de caractériser les fractions obtenues en termes de masses moléculaires, de concentrations en protéines et peptides et de profils de poids moléculaires et d’acides aminés, et 4) d’évaluer le potentiel antioxydant et neuroprotecteur des fractions obtenues. L’étude des colmatages peptidiques de membranes ioniques a démontré que les interactions électrostatiques sont la principale cause de ce phénomène dont l’intensité varie selon le type de membrane (cationique ou anionique) et les conditions du milieu utilisées (acide ou basique). Des étapes simples de nettoyages des membranes à l’aide de solution salines de NaCl peuvent améliorer les performances de ces procédés à long terme et ainsi améliorer leur efficacité. Les 2 couplages à l’étude ont démontré des taux de transfert de masse semblables alors que le couplage avec nanofiltration s’est montré plus efficace au niveau du taux de migration en fonction du temps et de la surface de membrane utilisée. Les 2 couplages ont produit des fractions peptidiques très différentes tant au niveau des profils en acides aminés, des poids moléculaires et du contenu peptidique qu’au niveau du potentiel antioxydant. En effet, le couplage UF/NF a permis de produire des perméats très concentrés en petits poids moléculaires alors que le couplage UF/EDUF a produit des fractions possédant une gamme plus large de poids moléculaires, mais présentant une spécificité en fonction du pH de la solution. Le perméat de nanofiltration et les KCl 1 et 2 de l’ÉDUF ont démontrés des niveaux transfert de protéines totales semblables avec les procédés utilisés. Le procédé d’ÉDUF a permis la récupération de fractions ayant un contenu plus élevé en peptides polaires. Les fractions d’ÉDUF KCl 1 à pH 3 et 6 ont démontré un potentiel antioxydant élevé lors du test de l’ORAC. Ces mêmes fractions ainsi que le KCl 1 à pH 9 et le perméat de NF à pH 6 ont aussi démontré un effet intéressant sur le potentiel redox. Cependant, aucune fraction recueillie n’a démontré d’effet de protection contre les espèces réactives à l’oxygène sur les cellules neuronales mais se sont montrées non-toxiques pour ces cellules. / Soy is an important legume produced in Canada and its culture and production rate increased significantly in the recent years. Developing new competences to create by-products instead of exporting soya to other countries is of interest for the economy. The functional food and nutraceutical industry have great interests on soya due to its high bioactivity potential in regard of the protein content. Technologies using membranes offer the possibility of fractionating solutions to concentrate and isolate molecules of interest. These technologies can be divided in two main categories: Pressure-driven processes in which ultrafiltration (UF) and nanofiltration (NF) take part and electrically-driven processes in which electrodialysis with ultrafiltration (EDUF) membrane takes place. Working with protein or hydrolyzate solutions (soya in this case) can be problematic since these proteins or peptides have the tendency to foul the membranes. The aim of this study was 1) to evaluate the ion-exchange membranes potential to fouling by soy peptides 2) to compare pressure- and electrically-driven process in terms of mass flux and mass balance 3) to characterize the fractions in terms of molecular weight and amino acid profile, protein and peptide contents and 4) to evaluate their antioxidant potential and neuroprotection capacity. The study on ion-exchange membranes fouling by peptides showed that electrostatic interactions are the main cause of this phenomenon and its intensity depends on the type of membrane (cationic or anionic) used and the medium characteristics (acid or basic). Simple cleaning steps with NaCl solution could enhance performances of this process and improve its efficiency. Both processes showed a similar mass balance, however UF/NF process showed a higher mass transfer than UF/EDUF process when considering the time and membrane surface used to complete the run. UF/NF system produced a permeate with small molecular weights while UF/EDUF system produced fractions with a large range of molecular weights with a very specific molecular weight range depending on the pH value. Both processes produced similar fractions in terms of protein content. Specific fractions of EDUF were composed of a high level of polar amino acids. KCl 1 pH 3 and 6 from EDUF showed antioxidant capacities by the ORAC test. The same fractions as well as KCl 1 pH 9 and NF permeate pH 6 showed an interesting effect in the redox potential. Therefore none of these fractions showed protection against oxidative stress induced in cells.