The success of surface water treatment strongly depends on the effectiveness of coagulant performance. Aluminium sulfate (alum), the most widely used coagulant in water treatment plants in Canada, is well known for its poor performance in cold water. Polyaluminium chloride (PACl), a relatively new polymeric aluminium coagulant increasingly being used in water treatment plants, is found to have many advantages over conventional alum. However, PACl hydrolysis reaction is quite complex and its action is not fully understood. In this research, a series of bench-scale jar tests with alum and PACl was conducted. Alum and PACl coagulation flocs were analyzed for the evaluation of coagulant performances at 19C and 5C for the Split Lake water treatment plant. The results of this research indicated that the settling properties of PACl flocs were superior to those of alum flocs, especially at the lower temperature. The average size of PACl flocs was relatively smaller than that of alum flocs. The density of PACl flocs could be higher than that of alum flocs. And the number of settled PACl flocs could be higher than that of settled alum flocs. The effects of temperature on alum flocs and PACl flocs were different. Alum flocs size decreased at 5C. This is most likely due to the existence of monomeric aluminium species in alum aqueous solution. PACl flocs size did not change significantly at the 5C. This may be due to the existence of polymeric aluminium species in PACl aqueous solution. / February 2006

Functionalization of nanoparticles often control the extent of their usage. With this in mind, I have explored methods of creating highly functionalized exfoliated graphite, by way of the Billups-Birch reduction, that can be used in the advancement of nanotechnology (i.e. biomedicine). The method explored the use of sodium as the source for the solvated electron. The results of this method produced exfoliated graphite the same size as graphene and with solubility similar to the substrates attached to it. It was further shown that functionalized graphite with a terminal carboxyl group allowed further synthesis to occur via an elimination-addition reaction after the acyl group was transformed into an acid chloride. This reaction makes it possible to create exfoliated graphite that contains any compound of interest as long as it has an oxygen or nitrogen group that is able to react with the acid chloride. Thus, these products have the potential to be used in biomedicine as drug delivery agents.

Sodium arsenite and cadmium chloride are two widespread environmental toxicants which have deleterious effects on living organisms. At the cellular level, sodium arsenite and cadmium chloride cause oxidative stress, dysregulation of gene expression, apoptosis, and the unfolding of protein. Furthermore, both chemical stressors individually have the ability to induce heat shock protein (HSP) accumulation. HSPs are molecular chaperones that aid in protein folding, translocation and in preventing stress-induced protein aggregation. Previously, our laboratory demonstrated that treatment of A6 kidney epithelial cells of the frog Xenopus laevis, with either cadmium chloride or sodium arsenite plus a concurrent mild heat shock resulted in an enhanced accumulation of HSPs that was greater than found with the sum of the individual stressors. To the best of our knowledge, no information is available to date on the effect that these two chemical stressors have in combination on HSP accumulation in aquatic organisms. The present study examined the effect of simultaneous sodium arsenite and cadmium chloride treatment on the pattern of HSP30 and HSP70 accumulation in Xenopus A6 cells. Immunoblot analysis revealed that the relative levels of HSP30 and HSP70 accumulation in A6 cells treated concurrently with sodium arsenite and cadmium chloride for 12 h were significantly higher than the sum of HSP30 or HSP70 accumulation from cells subjected to the treatments individually. For instance, the combined 10 µM sodium arsenite plus 100 µM cadmium chloride treatment resulted in a 3.5 fold increase in HSP30 accumulation and a 2.5 fold increase in HSP70 accumulation compared to the sum of the stressors individually. This finding suggested a synergistic action between the two stressors. Pretreatment of cells with KNK437, an HSF1 inhibitor, inhibited the combined sodium arsenite- and cadmium chloride-induced accumulation of HSP30 and HSP70 suggesting that this accumulation of HSPs may be regulated, at least in part, at the level of transcription. Immunocytochemical analysis employing the use of laser scanning confocal microscopy (LSCM) revealed that simultaneous treatment of cells with the two stressors induced HSP30 accumulation primarily in the cytoplasm in a punctate pattern with some dysregulation of F-actin structure. Increased ubiquitinated protein accumulation was observed with combined 10 µM sodium arsenite and 10, 50 or 100 µM cadmium chloride treatment compared to individual stressors suggesting an impairment of the ubiquitin-proteasome degradation system. Finally, while incubation of A6 cells with 1 µM sodium arsenite plus 10 µM cadmium chloride did not induce a detectable accumulation of HSPs, the addition of a 30 °C mild heat shock resulted in a strong accumulation of HSP30 and HSP70. This study has demonstrated that concurrent sodium arsenite and cadmium chloride treatment can enhance HSP accumulation. Since HSP accumulation is triggered by proteotoxic stress, these findings are relevant given the fact that aquatic amphibians in their natural habitat may be exposed to multiple chemical stressors simultaneously.

The purpose of this master thesis project was to investigate the penetration ofbiomolecules into hyaluronic acid (HA) macrogels. The investigations were performedboth in the presence and in the absence of the non-biodegradable surfactantcetylpyridinium chloride (CPC), which earlier has proved to form a micelle-rich shellat the gel surface. In this work investigations were performed to see if properties ofthe biomolecules used, such as size and charge, had any impact on the binding to theHA gels both with and without CPC. The biomolecules used were the proteinscytochrome c, lysozyme, hemoglobin and myoglobin and the polysaccharide dextranof different molecular weights and labeled with fluorescein isothiocyanate.Cetylpyridinium chloride was used as a non-biodegradable model surfactant for abiodegradable betaine ester surfactant. The cetylpyridinium chloride was thereforeserving well when performing control studies for the biodegradable betaine ester,because the two possesses similar properties. Investigations involving the betaineester surfactant was not included in this master thesis project. Also release studiesinvolving the labeled dextran and some of the proteins were performed in thepresence and absence of cetylpyridinium chloride.The binding of CPC to HA was investigated briefly as well as the microstructure ofHA gels saturated with CPC by means of small-angle X-ray scattering, SAXS, atdifferent salt concentrations. The microstructure-investigations indicated that at 10mM NaCl a cubic ordered phase with space group Pm3n was achieved. When the saltconcentration was increased to 40 mM the microstructure was altered to a clearface-centered cubic (FCC) structure. When increasing the NaCl concentrationfurther, to 150 mM, indication of an unordered micellar phase could be seen.Cytochrome c and lysozyme transport into HA gels, to which CPC had bound in anearlier step, could be registered using UV-VIS spectrophotometry. Indications showedthat CPC and cytochrome c was distributed to different parts of the gel frommicroscope pictures taken of the cross-section of gel samples at different time.From release experiments performed with fluorescein isothiocyanate-dextran noconclusions could be drawn on how the different molecular weights of dextranaffected the rate and extent of the amount substance released. Neither could theinfluence of CPC be elucidated. This since the extent of released amounts exceeded100 % for many samples and the duplicate samples investigated showed differentbehavior.The transport of cytochrome c, myoglobin and hemoglobin into HA gels with andwithout beforehand treatment with CPC was evaluated qualitatively. The transportinto gels treated with CPC was successful and complete with cytochrome c andmyoglobin at lower degree of binding but was limited for the bigger proteinhemoglobin. When investigating the release of cytochrome c, myoglobin andhemoglobin from HA gels the extent of released substance was lower with CPCpresent in the solution compared without CPC present. Also some indicationsshowed that the bigger size of hemoglobin affected the rate of release from the gel.

In printed electronics there are many polyelectrolytes to choose from. While polyelectrolytes such as polystyrene sulfonic acid can fulfill many ofthe desired functionalities of a semiconductor, there is a need for other polyelectrolytes with other functionalities, such as functionality at low airhumidity and better cross-linking possibilities, while still functioning as a good semiconductor.Within this thesis, there is a description of general polyelectrolytes, as well as various usages.The synthesis and characterization of new polyelectrolytes that have been developed, based upon diallyldimethyl ammonium chloride (DADMAC)and a derivative of polystyrene sulfonic acid (PSSH) is described.The study and experimental testing of the polymers as polyelectrolytes under different conditions is described.

Chloride concentrations at the Greenbrook well field in Kitchener, Ontario, have been steadily increasing over the past several decades and may soon pose a threat to drinking water quality. Drinking water limits at some wells have already been exceeded. The Regional Municipality of Waterloo (RMOW) relies mainly on local groundwater resources for its drinking water supply, and the Greenbrook well field is the oldest of 50 municipal well fields contributing to this supply. Urban growth and the expansion of city limits over the years has surrounded the well field, placing it in a high risk area in need of protection. As such, protection of this water supply is essential until alternative sources can be found. Road salt has been identified as the prime source of the chloride contamination, and various management alternatives and remediation strategies are currently being studied. In order to characterize the behaviour of chloride in the subsurface, an understanding of the mechanisms that control travel of chloride to the water table and through the groundwater system is needed. For the first phase of this work, a 2-D variably-saturated flow and transport model (SWMS-2D) was used to evaluate the effect of seasonal fluctuation in chloride loading to a generic aquifer system. Chloride was applied over the surface of the model in seasonal pulses that correlated with temperature and precipitation. The model showed a dampening of the seasonal response with depth that lead to the conclusion that long-term transport models can neglect seasonal changes in solute loading. For the second phase of this work, a proven 3D finite element transport model (Waterloo Transport Code: WTC) was used to simulate road salt impacts to the well field. Road salt was applied over selected roads throughout the steady-state capture zone via a type 3 (Cauchy) boundary that varies both temporally and spatially with road type and location. After calibrating the model from 1945 to 2002 to chloride concentrations using the weighted average of 5 Greenbrook production wells, the model was run to the year 2041 to assess future implications. Remediation strategies were also investigated via 6 predictive scenarios in which chloride applications were reduced by varying degrees. The results of this phase will be used by the RMOW in cost-benefit analyses of alternative de-icing approaches versus de-chlorination treatment of the well water.

The mutant prevention concentration (MPC) is defined as the lowest antimicrobial concentration required to inhibit the growth of the least susceptible bacterial cell based on an inoculum of ≥109 colony forming units (CFUs). The current protocol for MPC testing is technically demanding and time-consuming which limits its implementation into clinical microbiology laboratories. In an attempt to simplify the current MPC protocol we developed a modified MPC method, the microbroth dilution method, which requires two fewer days to complete than the current or traditional method. MPC values were consistent for all organisms and strains tested using both the traditional MPC method and the modified microbroth dilution MPC method.<p> Tigecycline is the first of a new class of compound glycylcyclines- with potent in vitro activity against Gram-positive organisms including penicillin-resistant and multi-drug resistant <i>Streptococcus pneumoniae</i> (SP) and methicillin-resistant <i>Staphylococcus aureus</i> (MRSA). We measured minimum inhibitory concentration (MIC) and MPC values for tigecycline against 47 clinical isolates of SP and found that the MPC90 values were >500 fold higher than the MIC90 values. To determine if MPC testing of tigecycline against SP is impacted by blood in the medium, we developed a new medium able to sustain the growth of SP without the need for blood; solidified Todd-Hewitt broth (sTHB). The MPC90 values of tigecycline against SP on sTHB were only 2 fold higher than the MIC90 values. When blood was added to the sTHB, the MPC90 values again became much greater than the MIC90 values (> 256 fold higher). MPC results for <i>Staphylococcus spp.</i> against tigecycline were not impacted by blood in the medium.<p> Benzalkonium chloride (BAK) is a cationic surface-acting agent that acts on bacterial cells by disrupting the intermolecular interaction of the lipid bilayer. To determine if the <i>fluoroquinolones gatifloxacin</i> (Gfx) and moxifloxacin (Mfx) are more active (lower MIC values) in the presence of BAK, we conducted MIC, MPC, and time-kill assays. MIC testing showed that in the presence of 3.125 to 50 µg/ml of BAK, the MIC of Gfx and Mfx decreased by 8- to 5000-fold against clinical isolates of methicillin-susceptible <i>Staphylococcus aureus</i> (MSSA), MRSA, Coagulase-negative <i>Staphylococci</i>(CNS), SP, <i>Escherichia coli</i> (EC), and <i>Pseudomonas aeruginosa</i> (PA). MPC testing showed that the presence of 7 to 10 µg/ml of BAK, the MPC of Gfx and Mfx decreased by 32- to 1000-fold against clinical isolates of MRSA. Conventional time-kill studies (using a bacterial load of 105 CFUs) showed that the killing activity of Gfx against clinical MRSA isolates was enhanced in the presence of BAK with a log10-reduction (percent kill) of 1.6 (76.08%) for Gfx alone at 180 minutes compared to a log10-redecution (percent kill) of 5.4 (100%) for Gfx plus BAK at 180 minutes.<p> Alexidine (Alx) is a bisbiguanide that has been used as an effective disinfectant in the dental industry and is potentially being developed for use as an antimicrobial agent for ocular infections. We conducted susceptibility testing of Alx using MIC testing, MPC testing, and time-kill assays against Gram-positive and Gram-negative pathogens. MIC testing showed that Alx is more active against Gram-positive pathogens than Gram-negative pathogens and showed better activity than the fluoroquinolones Gfx, Mfx, and levofloxacin (Lfx) against MRSA. The MPC values measured for MRSA and MSSA against Alx were non-reproducible using the traditional MPC method. Using the microbroth dilution MPC method, MPC90 values were found to be 32 fold higher than the MIC90 values. If the experimentally determined MPC values are true MPC values, initial MPC testing indicates that Alx may have a high likelihood for selecting for resistance, however, if the MPC values are not accurate it may be necessary to modify the MPC protocol in order to complete MPC testing of Alx against MRSA and MSSA. Conventional time-kill studies (using a bacterial load of 105 CFUs) measured bactericidal activity (> 3 log10-reduction) against MRSA, MSSA, SP, and PA.

No description available.

The Carrizo-Wilcox aquifer is a valuable groundwater resource, situated in a semi-arid landscape of Southwest Texas, where over-use by dependent farming practices has lowered aquifer levels. In semi-arid regions, rates of groundwater recharge are predominantly low due to high potential evapotranspiration rates; however, least understood is the role that vegetation plays in soil-plant-water dynamics. Vegetation management potentially plays a major role in countering the loss to recharge because evapotranspiration (ET) varies with vegetation type and cover. The conversion from shrubland to grassland likely reduces rooting depths and total plant cover. Subsequently, deep drainage (percolation below the root zone) will likely increase and lead to groundwater recharge, at least temporarily. The primary aims of the study were to identify those biotic and abiotic factors facilitating deep drainage and to examine differences in recharge for the years following clearing of natural shrub vegetation. Soil chloride was examined to estimate long-term recharge rates, since its concentration in the soil is influenced by the movement of water. Short-term soil moisture trends were also monitored for any water movement deep in the soil profile in response to individual rain events. Rooting depths decreased following removal of vegetation; yet root biomass unexpectedly increased due to successful grass establishment during the first five years after treatment. Soil properties did not vary between treatments, indicating that the majority of chloride differences seen were a consequence of vegetation change. Peak and total soil chloride concentrations were expected to decrease and occur deeper in the soil profile 15-30 years following the clearing of woody vegetation. Total chloride decreased by up to 65% after 30 years and resulted in an estimated 14.9 mm/yr more recharge compared to adjacent untreated controls. Evidence in this study suggest that much of this chloride is leached during the first five years following treatment and that more leaching occurs in especially wet periods. During the wet 2007 growing season, soil moisture below the root zone increased by up to 17% after vegetation clearing. The results of this study indicate that hydrologic changes following brush removal were evident in this system and are likely to positively influence groundwater recharge in the long-term.

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