This critical overview document (COD) presents, discusses and brings together the selected portfolio of publications that the author believes make a significant contribution to the field of wastewater treatment, focusing on the removal of endocrine disrupting chemicals (EDCs) in wastewater treatment applications. The aim of the research within this COD was to investigate the fate, mechanisms and optimisation of EDCs removal in wastewater treatment applications. The key objectives were to: 1. Investigate and understand the mechanisms of removal of EDCs in wastewater and sludge treatment processes. 2. Evaluate novel methods for the removal of EDCs in water and wastewater treatment applications. 3. Establish the kinetic and thermodynamic properties of the removal processes to inform process modelling of full scale design of treatment processes.

Thesis (MSc)--University of Stellenbosch, 2005. / ENGLISH ABSTRACT: Biological removal of sulphate from wastewater can be achieved by using a gas mixture consisting of 80% hydrogen and 20% carbon dioxide as energy and carbon sources. A novel reactor, including a venturi device for optimal hydrogen gas-liquid contact, and geotextile for immobilisation of the sulphate reducing bacterial community, was introduced. Efficient, relatively stable sulphate removal was obtained when the reactor was operated in continuous mode. The maximum sulphate removal rate obtained when the reactor was 8% packed with geotextile, was 1 g S04/(L.d) and 4 g S04/(L.d) when the reactor was 80% packed with geotextile. Kinetic batch studies showed that the highest sulphate removal rates were obtained at 29.5 °C; a pH of 7.5; initial sulphate concentration of 4000 mg/L; initial alkalinity of 1600 mg/L; cobalt concentration of 3 mg/L and when excess hydrogen gas was fed compared to what is stoichiometrically required (900 ml/min). Nickel addition showed inhibition at increased concentrations (>3 mg/L). The biofilm structure was observed on the geotextile with electron microscopy, while the viability of the biofilm was indicated with fluorescence microscopy. These observations indicated the suitability of the geotextile as a support material for biofilm formation in the sulphate reducing system. The stability of the sulphate reducing community was analysed, using the T-RFLP protocol. It was shown that the composition of the community changed after a period of 3 months, when the reactor was subjected to environmental changes. The reactor was also observed to be more efficient in terms of sulphate removal after the environmental changes, of which the temperature change from an average of 39 to 29.5 °C was the most prominent. Subsequently, it was speculated that the population shift was in favour of a more efficient system for sulphate removal. A dynamic, viable, mesophilic sulphate reducing community was therefore observed on the geotextile support, responsible for successful sulphate removal in a novel venturi-reactor. Defining optimal operating conditions, and a knowledge of biofilm structure and composition may contribute to the successful implementation of the biological sulphate removal component of the integrated chemical-biological process for the treatment of industrial wastewater, when hydrogen and carbon dioxide are supplied as the energy and carbon sources, respectively. / AFRIKAANSE OPSOMMING: Ongewenste industriële afval-water kan biologies behandel word deur 'n gasmengsel van 80% waterstof en 20% koolstofdioksied te gebruik vir sulfaat verwydering. 'n Reaktor wat 'n venturi apparaat bevat vir optimale waterstofgas-vloeistof kontak, asook geotekstiel vir die immobilisasie van die bakteriële sulfaatverwyderende gemeenskap, is bekend gestel. Effektiewe, relatief stabiele sulfaatverwydering is waargeneem sodra die reaktor op 'n kontinue basis gevoer is. Die optimale sulfaat verwyderingstempo wat bereik is as die reaktor 8% met geotekstiel gevul was, was 1 g S04/(L.d) en 4 g S04/(L.d) wanneer die reaktor 80% met geotekstiel gevul was. Kinetiese groepstudies het getoon dat die beste sulfaatverwydering bereik is by 'n gemiddelde temperatuur van 29.5 °C; pH van 7.5; aanvanklike sulfaatkonsentrasie van 4000 mg/L; aanvanklike sulfied konsentrasie van 268 mg/L; aanvanklike alkaliniteit van 1600 mg/L; kobalt konsentrasie van 3 mg/L, asook wanneer 'n oormaat waterstofgas gevoer is (900 ml/min), in vergelyking met wat stoichiometries benodig word. 'n Verhoogde byvoeging van nikkel by die voerwater (3 mg/L), het tekens van inhibisie getoon. Die biofilm struktuur is waargeneem op die geotekstiel met behulp van 'n elektronrnikroskoop, terwyl die lewensvatbaarheid van die biofilm aangedui is met behulp van fluoressensie mikroskopie. Hiermee is die bruikbaarheid van geotekstiel as 'n ondersteunings-matriks bevestig. Die stabiliteit van die sulfaatverwyderende gemeenskap is ondersoek deur die T-RFLP protokol te gebruik. Hiermee is aangedui dat die samestelling van die gemeenskap verander het na die 3 maande toets periode, toe die reaktor onderhewig was aan omgewings veranderinge. Die reaktor het ook 'n verbetering in sy sulfaatverwyderings vermoë getoon na hierdie tydperk van omgewingsveranderinge, waarvan 'n temperatuur verandering vanaf 'n gemiddeld van 39 na 29.5 °C die prominentste was. Dit is dus gespekuleer dat die populasie verskuiwing ten gunste was van 'n beter sisteem vir sulfaatverwydering. 'n Dinamiese, lewensvatbare, mesofiliese sulfaatreduserende gemeenskap, verantwoordelik vir die sulfaatverwydering in die venturi-reaktor, is dus waargeneem op die geotekstiel as 'n ondersteuningsmatriks. Met hierdie evaluasie kan die insig wat verkry is in die reaktor samestelling en die optimale kondisies vir die reaktor werking, bydra tot die suksesvolle implementasie van die biologiese komponent, in die geïntegreerde chemies-biologiese proses vir die behandeling van industriële afval water, wanneer 80% waterstof en 20% koolstofdioksied gas as energie en koolstofbron respektiewelik, gebruik word.

Thesis (MSc (Biochemistry))--University of Stellenbosch, 2011. / ENGLISH ABSTRACT: Due to a global lack of access to potable water, a problem particularly affecting people in developing countries and the poor, improvement on existing water purification methods are necessary to provide more cost effective, accessible and efficient methods of water purification. In drinking water systems, biofilms are a potential source of contamination, which can affect the biological stability and hygienic safety of water. In industrial water systems, biofilms can cause corrosion, resistance in flow systems and a decrease in efficiency of membranes. Nanotechnology has been identified as a technology to utilize in water purification problem solving. Alternatives to the use of chemical biocides and antibiotics need to be investigated therefore; the focus of this study was the fabrication and characterization of polymer nanofibers containing silver nanoparticles as biocide and anti-biofouling nanofibers with hydrolytic enzymes immobilized on the surface. The aim of this study was to synthesize and compare poly (vinyl alcohol) (PVA) nanofibers and poly (acrylonitrile) (PAN) nanofibers with silver nanoparticles to determine which type of fiber will be the most appropriate for application in water sanitation. The two types of fibers were to be compared based on morphology, silver nanoparticle content, physical distribution of silver nanoparticles, levels of silver leaching from the fibers in water, which could imply toxicity, and most importantly, anti-microbial efficacy. Back scattering electron images revealed that silver nanoparticles in PVA nanofibers were more evenly dispersed than in PAN nanofibers, but that PAN nanofibers had higher silver nanoparticle content. This was confirmed by energy dispersive X-ray (EDX) analysis. Both PVA and PAN nanofibers containing silver nanoparticles had excellent anti-microbial activity, with PVA nanofibers killing between 91% and 99% of bacteria in a contaminated water sample and PAN nanofibers killed 100%. When investigated by SEM, the biocidal effect of PAN nanofibers containing silver nanoparticles can be observed as morphological changes in the cell walls. Neither PVA nor PAN nanofibers leached silver into water. PVA is a non-toxic and biodegradable synthetic polymer, and PVA-silver nanofibers have excellent anti-microbial activity, making it applicable in water sanitation in an environmental conscious milieu. PAN nanofibers are more conductive to the formation of silver nanoparticles, have higher silver nanoparticle content, allowing the complete sanitation of pathogenically contaminated water samples. PAN nanofibers also have better longevity and strength in water, making it ideal for water filtration and sanitation in higher throughput systems. Furthermore, immobilized enzymes are being investigated as possible alternatives to inefficient conventional methods of controlling and removing biofilms from filtration systems. This study demonstrates the covalent immobilization of two industrial proteases and an amylase enzyme onto polymer nanofibers widely used in filtration membranes. Confirmed by FTIR, these nanofibers were successfully activated by amidination, allowing the covalent immobilization of respectively two serine proteases and an α-amylase onto the fibers. When inspected visually, fibers largely retained their original morphology after activation and enzyme immobilization. Immobilized enzymes were, however visible as aggregated particles on the nanofiber surfaces. The large surface area to volume ratio provided by the nanofibers as immobilization surface, allowed sufficient amounts of enzymes to be immobilized onto the fibers so that all enzymes retained above 80% of the specific activity of the free enzymes. For each of the immobilized enzymes, just below 30% of initial activity was retained after 10 repeated cycles of use. Fibers with immobilized enzymes on their surface did not support the growth of biofilms, as opposed to plain nanofibers, which did support the growth of biofilms. When considering the combined advantages of this effective immobilization process, the robustness of the enzymes used in this study, and their effectiveness against biofilms in their immobilized state, a valuable addition has been made to technology available for the control of biofilm formation on filtration membranes, and could potentially be employed to control biofilm formation in water filtration systems. A combination of anti-microbial and anti-biofouling nanofibers into a single nanofiltration product may prove to be highly applicable in water sanitation systems. / AFRIKAANSE OPSOMMING: As gevolg van 'n wêreldwye gebrek aan toegang tot drinkbare water, 'n probleem wat veral mense in ontwikkelende lande en armes raak, is dit van belang dat bestaande metodes van watersuiwering verbeter word om voorsiening te maak vir meer koste-effektiewe, toeganklike en doeltreffende metodes van watersuiwering. In drinkwater stelsels is biofilms 'n potensiële bron van besoedeling, wat die biologiese stabiliteit en die higiëniese veiligheid van water beïnvloed. In industriële waterstelsels kan biofilms tot die verwering van pyplyne lei, weerstand in die stroomstelsels veroorsaak en 'n afname in die doeltreffendheid van membrane veroorsaak. Nanotegnologie is geïdentifiseer as 'n tegnologie wat aangewend kan word in watersuiwerings probleemoplossing. Alternatiewe vir die gebruik van chemiese antimikrobiese middels moet dus ondersoek word. Hierdie studie fokus dus op die vervaardiging en karakterisering van polimeer nanovesels met silwer nanopartikels wat ingesluit is as antimikrobiese middel en anti-biofilm vesels met hidrolitiese ensieme geïmmobiliseer op die oppervlak. Die doel van hierdie studie was om poli (viniel alkohol) (PVA) nanovesels en poli (akrielonitriel) (PAN) nanovesels te sintetiseer waarby silwer nanopartikels ingesluit is, en te bepaal watter tipe vesel die mees geskikte sal wees vir die gebruik in water sanitasie. Die twee tipes vesels is met mekaar vergelyk gebaseer op morfologie, silwer nanopartikel inhoud, fisiese verspreiding van silwer nanopartikels, vlakke van silwer uitloging vanuit die vesels in water, wat toksisiteit tot gevolg kan hê, en die belangrikste, antimikrobiese effektiwiteit. Terug verstrooiing elektron beelde het aan die lig gebring dat die silwer nanopartikels in PVA nanovesels meer eweredig versprei was as in PAN nanovesels, maar dat PAN nanovesels 'n hoër silwer nanopartikel inhoud gehad het. Dit is bevestig deur “energy dispersive X-ray” (EDX) analise. Beide PVA en PAN nanovesels met silwer nanopartikels het uitstekende antimikrobiese aktiwiteit getoon, met PVA vesels wat tussen 91% en 99% bakterieë in besoedelde water monsters kon doodmaak en PAN vesels wat 100% bakterieë kon uitwis. Wanneer vesels ondersoek is met ʼn skandeer elektronmikroskoop (SEM), kon die antimikrobiese effek van PAN vesels met silwer nanopartikels as morfologiese veranderinge in die selwande waargeneem word. Nie PVA of PAN nanovesels loog silwer uit in water nie. PVA is 'n nie-toksiese en bioafbreekbare sintetiese polimeer, en PVA-silwer nanovesels het uitstekende antimikrobiese aktiwiteit, wat dit van toepassing maak op water sanitasie in ʼn omgewings bewuste milieu. PAN vesels is meer gunstig tot die vorming van silwer nanopartikels, en het 'n hoër silwer nanopartikel inhoud, dus word patogeen besoedelde water volledig gesteriliseer. PAN vesels het ook 'n beter langslewendheid en weerstandige sterkte in water, wat dit ideaal vir water filtrasie en sanitasie in hoër deursettings stelsels maak. Geïmmobiliseerde ensieme word ook ondersoek as moontlike alternatiewe tot ondoeltreffende konvensionele metodes van beheer en die verwydering van biofilms uit water stelsels. Hierdie studie toon die kovalente immobilisasie van twee industriële proteases en 'n amilase ensiem op polimeer vesels wat gebruik word in filtrasie membrane. Bevestig deur FTIR, is PAN vesels suksesvol geaktiveer deur amidinasie, sodat die kovalente immobilisasie van onderskeidelik twee serien proteases en 'n α-amilase op die vesels moontlik is. Met visuele ondersoek kan gesien word die vesels behou grootliks hul oorspronklike morfologie na aktivering en ensiem immobilisasie. Geïmmobiliseerde ensieme is egter sigbaar as saamgevoegde deeltjies op die nanovesel oppervlaktes. Die groot oppervlakarea: volume-ratio van die vesels wat dien as immobilisasie oppervlak, laat toe dat voldoende hoeveelhede van ensieme geïmmobiliseer word sodat alle ensieme meer as 80% van die spesifieke aktiwiteit van die vrye ensieme behou. Vir elk van die geïmmobiliseer ensieme, is net minder as 30% van die aanvanklike aktiwiteit behou na 10 siklusse van hergebruik. Vesels met geïmmobiliseerde ensieme op hul oppervlaktes het nie die groei van biofilms ondersteun nie, in teenstelling met gewone vesels, sonder ensieme, wat die groei van biofilms ondersteun. As die gesamentlike voordele van hierdie doeltreffende immobilisasie proses, die robuustheid van die ensieme en hulle doeltreffendheid teen biofilms in hul geïmmobiliseerde toestand in ag geneem word, is ʼn waardevolle toevoeging gemaak tot tegnologie wat beskikbaar is vir die beheer van biofilm vorming op filtrasie membrane, en dit kan potensieel gebruik word om biofilm vorming filter stelsels te beheer. Die kombinasie van anti-mikrobiese en anti-biofilm vesels in ʼn enkele nanofiltrasie produk moet nagestreef word, omdat dit hoogs van toepassing sal wees in water sterilisasie stelsels.

Thesis (PhD)--Stellenbosch University, 2008. / ENGLISH ABSTRACT: This study concerns the synthesis, properties and quantitative analysis of polydiallyldimethylammonium chloride (polyDADMAC), a water-soluble polymer used world-wide for potable water purification. The special interest in this polymer is the result of its widespread use and the current lack of adequate analytical methods for it. This is especially important for water treatment organisations. A novel gel permeation chromatography (GPC) method was developed and evaluated for polymer analysis. The scope was extended to determine the presence of unreacted monomer (DADMAC) as well as the percentage active polymer. polyDADMAC was first prepared using a known synthesis method. The product was purified and characterized by GPC and 13C-NMR spectroscopy. New and conclusive evidence of the existence of a five-member pyrrolidine ring system was obtained. A proposed mechanism of polymerization was determined. The activity of the synthesized polyDADMAC was evaluated and it was found to perform effectively as a coagulant. The physical and chemical properties of polyDADMAC were then studied under simulated water treatment conditions. The polymer reaction with chlorine revealed the formation of trihalogenated methane compounds (THMs). Gas chromatography–mass spectrometry (GC–MS) was used to conclusively identify the formation of chloroform. The polymer stability under different conditions of heat exposure, UV radiation and pH variations was studied. GPC results indicated that polyDADMAC is a very stable polymer and undergoes structural change only when subjected to extremes of pH, temperature and UV conditions. Results of a short study on microbial degradation indicated growth of the cultures, and subsequent polymer degradation. Reactions of polyDADMAC were concluded with a study of the impact of ozone on polyDADMAC. GPC results indicated a significant change in the ozonated polymer peak profile. Analytical methods to determine polyDADMAC residues in water were reviewed and critically evaluated. Methods based on complex formation/spectroscopy suffered from severe limitations and produced no meaningful results, contrary to claims made by previous researchers. Colloid titration based on an established method was promising but required extensive modification for quantitative analysis. Finally four novel methods were developed, including: solid phase extraction, membrane filtration-GPC, the HACH complexation method, and a GPC method with indirect UV detection. The study is concluded with a chemical risk assessment that indicated minimal human health risks associated with the production and use of polyDADMAC. / AFRIKAANSE OPSOMMING:Hierdie studie behels die sintese, eienskappe en kwantitatiewe analise van polidiallielmetielammoniumchloried (polyDADMAC), 'n wateroplosbare polimeer wat wêreldwyd vir drinkwatersuiwering gebruik word. Die belangstelling in hierdie spesifieke polimeer is as gevolg van die wydverspreide gebruik daarvan en die feit dat daar tans onvoldoende eenvoudige analitiese metodes daarvoor bestaan. Dit is veral belangrik vir waterbehandelingsorganisasies. 'n Nuwe gelpermeasiechromatografie (GPC) metode is ontwikkel en geevalueer vir die analise van hierdie polimeer. Die omvang van die studie is later uitgebrei om die teenwoordigheid van ongereageerde monomeer (DADMAC) asook die persentasie aktiewe polimeer te bepaal. polyDADMAC is eers volgens 'n bekende sintesemetode berei. Die produk is gesuiwer en gekarakteriseer m.b.v. GPC en 13C-KMR. Nuwe bewyse vir die bestaan van 'n vyflid pirollidoonringsisteem is verkry. 'n Meganisme vir hierdie polimerisasie metode is vasgestel. Die aktiwiteit van die bereide polyDADMAC is geevalueer en daar is bevind dat dit effektief as koaguleermiddel optree. Daarna is die chemiese en fisiese eienskappe van polyDADMAC onder gesimuleerde waterbehandelingskondisies bepaal. polyDADMAC het met chloor gerageer om trihalogeneerde metaanverbindings (THMs) te vorm. Gaschromatografie–massa-spektrometrie (GC–MS) is gebruik om die ontstaan van chloroform te bevestig. Daarna is die stabiliteit van die polimeer onder verskei reaksiekondisies bepaal: hitte, UV-bestraling, en pH. GPC-resultate het aangeduiui dat polyDADMAC baie stabiel is en ondergaan strukturele veranderings slegs onder uiterste kondisies van pH, temperatuur en UV. 'n Kort studie van die effek van mikro-organismes op polyDADMAC het egtermikrobiese kultuurgroei met die gevolglike afbreek van die polimeer getoon. Resultate van 'n studie van die impak van osoon op polyDADMAC het getoon dat daar 'n groot verandering in die GPC-profiel van die ge-osoneerde vorm van die polimeer was. Verdere analitiese metodes wat al gebruik is om polyDADMAC residue in water te bepaal, is uitgevoer en krities geevalueer. Metodes gebasseer op kompleksvorming/ spektroskopie het erge beperkings gehad en het nie betekenisvolle resultate gelewer nie. Dit was in teenstelling met wat voorheen deur ander navorsers bevind is. 'n Kolloiedtitrasie gebasseer op 'n bestaande metode het goeie resultate gelewer maar het omvattende veranderings benodig om kwantitatiewe resultate te lewer. Ten slotte is vier nuwe metodes ontwikkel: soliede fase-ekstraksie, membraanfiltrasie-GPC, die HACH-komplekseringsmetode, en 'n GPC-metode met indirekte UV-waarneming.. Die studie is afgesluit met 'n bepaling van die chemiese risiko wat poly DADMAC vir die gesondheid van die mens inhou. Daar is tot die gevolgtrekking gekom dat die produksie en gebruik van poly DADMAC slegs‘n minimum gesondheidsrisiko inhou.

Thesis (PhD)--Stellenbosch University, 2001. / ENGLISH ABSTRACT: The photo-mineralization of organic compounds (in the combined presence of a Ti02 based semiconductor catalyst, UV radiation and molecular oxygen) represents an advanced oxidation technology with significant potential for environmental pollution abatement. This oxidation process (generally known as photocatalytic oxidation - PCO) is currently the subject of extensive global research, with the main objective being the oxidative removal of organic and inorganic pollutants from water, air and soil. Presently, many barriers still block the way to commercial implementation of this technology, hence a unique (and effective) configuration of catalyst, light source and reactor design needs to identified. In terms of the water treatment scenario (which is the emphasis of this work) the need exists to develop a practical and affordable PCO reactor for water treatment on a large scale. The two laboratory-scale PCO reactors investigated in this work were based on a "falling film" flow reactor design and were constructed with commercially available materials and components. Degussa P-25 Ti02 was used as semiconductor catalyst and two types of low-pressure mercury lamps as the UV light source. Three modes of operation were investigated in order to determine the practical feasibility of the reactors. These included the recirculation, single pass and sequential single pass modes. The reactors were operated either as a Ti02 slurry-phase reactor (Reactor 1), or with Ti02 immobilized on stationary fiber glass and fibrous activated carbon sheet modules (Reactors 2A and 28 respectively). Extensive parametric evaluations were done using conventional one-factor variation and statistical methods according to optimal experimental design principles. The PCO treatment of two model organic pollutants (para-Chlorophenol and cyanobacterial microcystin YA, YR, LR and RR) were investigated. These pollutants were spiked into various water matrices to the desired concentration level. The combined photocatalyticcarbon adsorption treatment of these two pollutants was also investigated in Reactor 28. The experimental results obtained through this work showed that both model pollutants were successfully degraded in several water matrices by means of treatment in the respective PCO reactors. Moreover, this research was the first ever demonstration of the Ti02 photocatalytic degradation of microcystin toxins in the aqueous phase. The large number of parametric and optimization studies yielded the relative contributions of the various process parameters (in terms of the defined photocatalytic efficiency parameters as responses) very effectively. Furthermore, statistical evaluation of the experimental data provided valuable insight into the scientific phenomena associated with Ti02 mediated PCO processes. / AFRIKAANSE OPSOMMING: Die foto-mineralisasie van organiese verbindings (in die gekombineerde teenwoordigheid van 'n Ti02 gebaseerde halfgeleier katalisator, UV straling en molekulêre suurstof) verteenwoordig 'n gevorderde oksidasie-tegnologie met beduidende potensiaal vir bekamping van omgewingsbesoedeling. Hierdie oksidasie-proses (algemeen bekend as fotokatalitiese oksidasie - FKO) is tans wêreldwyd die onderwerp van ekstensiewe navorsing, met hoofdoel die oksidatiewe verwydering van organiese en anorganiese besoedelingstowwe uit water, lug en grond. Huidiglik bestaan daar nog vele struikelblokke wat die weg na kommersiële implementering van hierdie tegnologie blokkeer, gevolglik moet 'n unieke (en effektiewe) konfigurasie van katalisator, ligbron en reaktor-ontwerp nog identifiseer word. In terme van die waterbehandeling situasie (wat die klem van hierdie werk is) bestaan die nodigheid om 'n praktiese en bekostigbare FKO reaktor te ontwikkel vir watersuiwering op 'n groot skaal. Die twee laboratorium-skaal FKO reaktore in hierdie studie was gebaseer op 'n "vallende film" vloeireaktor ontwerp en is gekonstrueer met kommersieël beskikbare materiale en komponente. Degussa P-25 Ti02 is aangewend as halfgeleier katalisator en twee tipes lae-druk kwik lampe as die UV ligbron. Drie bedryfsmodes is ondersoek met die doel om die praktiese haalbaarheid van die reaktore te bepaal. Hierdie het ingesluit die resirkulasie, enkeldeurvloei en enkeldeurvloei-sekwensie modes. Die reaktore is bedryf as óf 'n Ti02 flodder-fase reaktor (Reaktor 1) óf met Ti02 ge-immobiliseer op 'n stasionêre veselglas en veselagtige ge-aktiveerde koolstof blad-modules (Reaktor 2A en 28 onderskeidelik). Omvattende parametriese evaluasies is gedoen deur gebruik te maak van konvensionele een-faktor variasie en statistiese metodes na aanleiding van optimale eksperimentele ontwerp beginsels. Die FKO behandeling van twee modelorganiese besoedelingstowwe (para-Chlorofenol en siano-bakteriese mikrosistien YA, YR, LR en RR) is ondersoek. Hierdie besoedelingstowwe is ge-ent in verskeie watermatrikse tot die verlangde konsentrasievlak. Die gekombineerde fotokatalitiese - aktiveerde koolstof behandeling van die twee besoedelingstowwe is ook ondersoek in Reaktor 28. Die eksperimentele resultate verkry deur hierdie werk het getoon dat beide die modelbesoedelingstowwe suksesvol gedegradeer is in verskeie watermatrikse deur behandeling in die onderskeie FKO reaktore. Trouens, hierdie navorsing was die eerste demonstrasie ooit van die Ti02 fotokatalitiese degradasie van mikrosistien toksiene in die waterige fase. Die groot aantal parametriese en optimiseringstudies het die bydraes van die verskeie proses-parameters (in terme van die gedefinieerde fotokatalitiese effektiwiteitsparameters as response) baie effektief verskaf. Verder, statistiese evaluasie van die eksperimentele data het waardevolle insig verskaf tot die wetenskaplike verskynsels te assosieer met Ti02 gemedieërde FKO prosesse.

No description available.

published_or_final_version / Civil Engineering / Doctoral / Doctor of Philosophy

published_or_final_version / Environmental Management / Master / Master of Science in Environmental Management

Partially disulfonated poly(arylene ether sulfone) (BPS) membranes have shown great promise as robust, chlorine tolerant alternatives to the current polyamide materials as reverse osmosis desalination membranes for water purification. The random copolymers are synthesized by direct polymerization of a disulfonated monomer (3,3’-disulfonato-4,4’-dichlorodiphenyl sulfone (SDCDPS)) and other monomers (4,4’-dichlorodiphenyl sulfone (DCDPS) and 4,4’-biphenol (BP)). The sulfonation of the materials adds necessary hydrophilic character and adjusting the percent sulfonation of the material changes the water and salt uptake of the material. Additionally, sulfonation causes the membranes to be charged, making them ion exchangers in which anions are partially excluded from the membrane, thus affecting the partitioning of salt in the membrane. The amount of sodium chloride present in the membrane after equilibration with external soaking solutions of varying concentrations of sodium chloride was measured by measuring the amount of individual ions, i.e., the sodium cation and chloride anion, separately. One area in which this work is unique is that it sought to measure the concentrations of the ions independently of one another. The analysis of sodium and chloride has shown the concentration of sodium in the membrane to be significantly greater than that of chloride, where the uptake of chloride is the limiting factor in the uptake of sodium chloride. The trends in the concentrations as well as in the partition coefficients of the ions are consistent with Donnan Exclusion. / text

The bacterial flora of groundwater obtained from wells and distribution sites was investigated from both an ecological and a public health perspective. A majority of the isolates were oxidase positive, non-fermentative, gramnegative bacilli. Extensive heterogeneity of groundwater microflora, as determined by biochemical characterization and antibiograms, was observed both within and among welldistribution (N-D) systems. Of the unique isolates (sorts) found in the W-D systems, 75% were resistant to 2 or more antibiotics at clinically significant concentrations. Community diversity within W-D systems was evaluated by rarefaction which failed to reveal a general trend. Standard plate counts in 2 of 3 wells were significantly higher on Standard Methods Agar diluted ten-fold than on the same medium at the standard concentration. Pseudomonas aeruginosa, Flavobacterium sp., Aeromonas hydrophila and Yersinia enterocolitica were detected in 21, 18, 7 and 3% respectively of water samples analyzed over a 12 month period. A selective medium was developed for the isolation of Flavobacterium sp. and was effective in suppressing 98% of the background flora when used in a membrane filtration (MF) procedure. Yersinia Selective Agar was employed in an MF procedure for the isolation of Y. enterocolitica. The use of anaerobic incubation in this procedure effectively suppressed background growth both in the presence and absence of an antimicrobic supplement. Anaerobic incubation of m-endo LES Agar (AN-MF) was effective in suppressing non-coliform growth in the total coliform MF test and markedly reduced the frequency of overgrown plates. The AN-MF appeared to obviate the need for selective chemical agents and thus has potential value in the isolation of stressed coliforms.