Thesis (M.S.)--West Virginia University, 2009. / Title from document title page. Document formatted into pages; contains ix, 117 p. : ill. (some col.), col. maps. Includes abstract. Includes bibliographical references.

Thesis (M.S.)--Worcester Polytechnic Institute. / Keywords: AFM, Bacterial Adhesion. Includes bibliographical references (p.130-143).

Thesis (Ph.D.)--Hong Kong University of Science and Technology, 2005. / Includes bibliographical references (leaves 200-223). Also available in electronic version.

Persistent organic pollutants (POPs) fall under a group of synthetic chemicals known for their persistence in environmental matrices such as soil and water, and are used in industrial, domestic and agricultural applications. Because of their volatility and lipophilicity, POPs can be transported far away from their point sources and bio-accumulate in food and in fatty tissues of humans and animals. In view of their toxicity and carcinogenicity some organic pollutants such as polychlorinated biphenyl (PCBs), organochlorine pesticides (OCPs) and phenolic derivatives (chlorophenol and nitrophenol) have been classified by United State Environmental Protection Agency (USEPA) and World Health Organization (WHO) as priority pollutants. The present work evaluated the distribution patterns of 19 polychlorinated biphenyls congeners, 17 organochlorine pesticides and selected phenolic derivatives (USEPA 11-priority pollutants) in the Buffalo River, in the Eastern Cape Province, South Africa between December 2015 and May 2016. The Liquid-liquid extraction technique was used for PCBs, OCPs and phenolic derivatives in the river water samples. Silica gel and florisil clean up were carried out for PCBs and OCPs samples respectively and analyzed with gas chromatography electron capture detector (GC/ECD). Phenolic compounds were derivatized and analyzed by gas chromatography mass spectrometer (GC/MS). Limits of detection (LOD), limit of quantitation (LOQ) and relative standard deviation (RSD) for the PCBs were 10 to 330 ng/L, 20 to 1,060 ng/L and 1.18 to 14.1 percent respectively. The LOD, LOQ and RSD for the OCPs were from 20 - 60 ng/L, 110 - 530 ng/L and 0.02 - 0.06 percent, while the corresponding values for the phenolic derivatives were 10 to 70 ng/L, 33 to 222 ng/L and 1.99 - 10.86 percent. In summer, the concentrations of PCBs, OCPs and phenolic derivatives ranged from <LOD to 482 ng/L, <LOD to 4,403 ng/L and <LOD to 1,546 ng/L respectively, while in autumn they were from <LOD to 2,383 ng/L, <LOD to 858 ng/L and <LOD to 713 ng/L in that order. Also, in summer, the level of occurrence of total PCB congeners detected at the various sampling sites were Buffalo River Estuary (BRE) 11 percent, Mdantsane (MSN) 16 percent, Zwelitsha (ZW) 26 percent, King William’s Town (KWT) 47 percent, Izele (IZ) 32 percent, and Maden (MD) 21 percent. The level of occurrence of total OCPs at BRE was 65 percent, at MSN 65 percent, at ZW 82 percent, at KWT 47 percent, at IZ 29 percent, and at MD 18 percent. The level of occurrence of total phenolic derivatives at BRE was 63 percent, at MSN 63 percent, at ZW 54 percent, at KWT 63 percent, at IZ 63 percent, and at MD 54 percent. In autumn, the level of occurrence of total PCBs at BRE was 68 percent, at MSN 16 percent, at ZW 42 percent, at KWT 26 percent, at IZ 47 percent, and at MD 0 percent. The level of occurrence of total OCPs at BRE was 65 percent, at MSN 53 percent, at ZW 41 percent, at KWT 35 percent, at IZ 53 percent, and at MD 18 percent. The level of occurrence of total phenolic derivatives at BRE was 63 percent, at MSN 63 percent, at ZW 54 percent, at KWT 18 percent, at IZ 18 percent, and at MD 45 percent. In summer, the levels of PCBs in all sampling sites were below WHO recommended maximum permissible levels (500 ng/L) for humans but in autumn the levels were above the recommended values in all the sites except MD. The cancer risk assessment values were above permissible 10-6 while hazard quotients were above the USEPA maximum limits of unity. OCPs levels were above the USEPA limits (100 ng/L) in all sampling locations in both seasons. The cancer risk assessment values were below permissible 10-6 but hazard quotients were above the USEPA maximum limits. Phenolic derivatives were also above the USEPA maximum permissible limit (500 ng/L) in most of the sampling locations in summer whereas during autumn the values were notably below the permissible limit at ZW, KWT, IZ and MD. The cancer risk assessment values and hazard quotients were above USEPA maximum limits of 10-6 and unity respectively. Conclusively, the results of this study reveal that the pollutants were present in the river at concentrations higher than the tolerable limit for human and wildlife and thereby may constitute a serious risk to public health. Therefore, it is recommended that proper regulation of the use of the compounds and their safe disposal be ensured to protect aquatic resources and the well-being of humans.

Monitoring for pollutants in potable water is an area of interest and concern for water supply companies. Supply of sub-standard water can draw complaints from public and industrial customers. Water and water tainted with pollutants were used to assess the application of a non-specific chemical sensor array (eNose) to monitor for changes in the headspace generated from a flow-cell by means of statistically designed experiments. 2-chlorophenol and diesel were used to further assess trends in headspace generation during trials where different combinations of sampling parameters were applied. Field trials were conducted in accordance with the most suitable methodology determined during initial studies under laboratory conditions. The headspace is generated by bubbling nitrogen through the flow-cell containing a water sample. The liquid sample is flushed and regenerated after each sensor acquisition cycle. The resultant headspace sample is transferred to the sensor array module where the resistance of the conducting polymer sensors is monitored as they are exposed to each respective headspace sample. The change in each sensor resistance after 60 seconds of exposure is used to represent the headspace character. Subsequent acquisitions are added to a data set and then presented graphically. Sudden changes in the sensor resistance plots represent changes in water quality. The results showed that the developed apparatus and sampling methodology can determine the presence or absence of pollution in a water matrix. Laboratory analysis showed that detection levels for 2-chlorophenol and diesel were both &lt;5 ppm in the mixed stream. Future developments should focus on increasing the sensitivity of the system by concentrating the pollutants in either the liquid or gas phase or by modifying the sampling protocol to enable sensor recognition at lower concentration levels. The sensor array could act as a screening technique to support quantitative and characterising analytical equipment at the abstraction point. Establishing a pollution alarm limit, within the bounds of acceptable system variation, would enable conventional analytical techniques to remain on standby until activated by a statistically significant change in water quality. Once established continued testing would enable alarm levels to be incorporated into a contaminant database for additional pollutant compounds and combinations of known taste and odour causing compounds.

Made available in DSpace on 2014-06-11T19:29:07Z (GMT). No. of bitstreams: 0 Previous issue date: 2011-08-10Bitstream added on 2014-06-13T19:38:03Z : No. of bitstreams: 1 lima_d_me_sjrp.pdf: 725372 bytes, checksum: 4c5a9d3b5a4993c307ce225938e61681 (MD5) / Ambientes naturais próximos a áreas urbanas e industrializadas são comumente contaminadas com descargas de poluentes, as quais são muitas vezes compostas por agentes químicos que não são removidos por sistemas de tratamento de efluentes convencionais, resultando num grande aporte de substâncias potencialmente tóxicas no ambiente aquático. Os metais são componentes naturais presentes nos ecossistemas. Estes elementos são indispensáveis para processos bioquímicos e fisiológicos nos seres vivos. No entanto, muitos desses elementos, quando em níveis elevados, podem ter efeitos adversos na saúde humana. Sabe-se que as enzimas esterases são fortemente inibidas por praguicidas organofosforados (OP) e carbamatos (CM), porém estudos recentes apontam o potencial efeito de alguns metais como compostos interferentes na atividade das esterases. Portanto, a avaliação da inibição de esterases em organismos aquáticos tem sido amplamente utilizada como um indicador de contaminação ambiental por esses compostos. O presente trabalho teve como objetivo o estudo da interferência dos metais cobre, chumbo, ferro e cádmio, na atividade da acetilcolinesterase (AChE) e carboxilesterase (CbE), em zebrafish. A AChE foi significantemente inibida in vitro pelo cobre, ferro, chumbo e cádmio nas maiores concentrações testadas (10 e 20 mmol/L), enquanto CbE foi inibida apenas na concentração de 20 mmol/L. In vivo somente o chumbo e o cádmio foram capazes de causar inibição na AChE nas maiores concentrações testadas, o ferro não causou nenhuma alteração e o cobre promoveu um aumento na atividade da AChE na concentração de 0,06 mg/L. A CbE não sofreu nenhuma alteração em nenhum dos tempos e concentrações testadas, exceto na exposição ao cobre, onde apresentou decréscimo em sua atividade. Além disso, de acordo com dados cinéticos obtidos, observa-se que todos os inibidores... / Natural environments close to urbanized and industrialized areas are commonly contaminated by discharges of pollutants, which are often composed by chemicals that aren’t removed by conventional wastewater treatment systems. Metals are natural components in the ecosystems, being essential to biochemical and physiological process in living organisms. However, if these elements are in excess, they can impose adverse effects on living organisms. Esterases are strongly inhibited by organophosphate (OP) and carbamate (CM) pesticides, but recent studies pointed to the potential effect of some metals as interfering compounds on the esterases activity. The present work aimed to study the interference of the metals copper, lead, iron and cadmium in the activity of acetylcholinesterase (AChE) and carboxylesterase (CbE) in zebrafish. AChE was significantly inhibited in vitro by copper, iron, lead and cadmium at higher concentrations (10 and 20 mmol/L), whereas CbE was inhibited only at a concentration of 20 mmol/L. In vivo, only lead and cadmium were able to cause AChE inhibition at higher concentrations, iron didn’t cause any changes and copper promoted an increase in the AChE activity at concentration of 0.06 mg/L. CbE activity did not change in any of the times and concentrations tested, except in the copper exposure, which showed a decrease in its activity. Furthermore, according to kinetic data obtained, it is noted that all inhibitors showed mixed inhibition type. Indeed, iodoacetamide treatment did not change AChE neither CbE activities, indicating that the metal inhibiting effect is probably not due to biding to thiol groups close the active site of the enzyme. These results indicate metals as important inhibitors of esterase in zebrafish, and should be considered in environmental monitoring studies that uses esterase inhibition as OP and CM exposure biomarkers

M.Tech. (Chemistry) / Please refer to full text to view abstract

M. Tech. / Background: Waterborne disease contributes significantly to the total global disease burden. Populations in rural areas of South Africa depend on untreated waters for consumption and sanitation. Contamination of public water supplies by harmful bacteria such as pathogenic E. coli poses a major risk for public health. Ingestion of these pathogenic microorganisms present in the contaminated and untreated waters could cause infection, leading to systemic inflammatory responses manifested by the production of various proinflammatory cytokines. To date, there is no human system test available to detect whether water, following ingestion, would cause disease (i.e. whether the water is infectious). The current water testing methods only test for the presence of indicator organisms, such as faecal coliforms, total coliforms, and Escherichia coli. A reliable in-vitro bioassay that could assess whether the water would cause an inflammatory response was investigated in this study. Objectives: Pro-inflammatory cytokines and whole-blood have been used in similar studies to detect the inflammatory responses following exposure to specific stimulants such as dust, lipopolysaccharide (LPS), E. coli and various others. It has been reported that larger numbers of these contaminants induced higher levels of pro-inflammatory cytokine expression. This implies that the pro-inflammatory cytokine expression could be used as a marker of infection since, inflammation occurs in response to infection. Successful infection is thus necessary for inflammation to occur, and high levels of pro-inflammatory cytokine expression confirm that infection has occurred. Thus if pro-inflammatory cytokines could serve as indicators for infection, these cytokines could be used as indicators for bacterial pathogenicity of water.

M.Sc. / The prevalence of natural organic matter (NOM) in water remains a huge challenge for water treatment companies and municipalities. NOM, however, is not a stand-alone problem as it affects water quality in many ways. NOM is largely responsible for the formation of disinfection by-products (DBPs) via its interaction with disinfectants during water disinfection. It is implicated for the undesirable colour, taste and odour of water and NOM even inhibits precipitation precursors which form the backbone of drinking water treatment. There is therefore no question that NOM, which is either a precursor to or direct cause of the problems highlighted above, should be considered as one of the critical design parameters to be considered for drinking water treatment. In our laboratories, research that involves the use of cyclodextrin (CD) polyurethanes for the removal of organic pollutants from water has been extensively investigated, and the CD polyurethanes have demonstrated the ability to effectively remove the organic species from water at low (ppb) concentrations. CDs, which are cyclic oligomers consisting of glucopyranosyl units linked together through α-1,4 glycosidic linkages, behave like molecular hosts. They are capable of forming inclusion complexes with guest molecules and hence can be utilised for the removal of organic contaminants from water. Their solubility in water, however, limits their application in the removal of organic contaminants from water. This limitation is easily resolved by polymerising the CDs into water-insoluble polymers with bifunctional linkers such as hexamethylene diisocyanate (HMDI). In this study, CD polyurethanes and ion exchange resins were used for the removal of NOM and possibly its DBPs from water. This study first investigated the local NOM source to establish its type and character, hence the study involved the characterization of the bulk water samples and fractionating the NOM using ion exchange resins for further characterization. The water samples were found to consist mainly of humic substances in the form of hydrophobic NOM, with the hydrophilic basic (HpiB) fraction being the most abundant NOM fraction in all samples. Trihalomethanes (THMs) were used as a representative of DBPs in this vii study. THMs formation studies of the individual NOM fractions indicated that all six NOM fractions were found to form THMs but in varying proportions. The HpiB fraction was found to be the most reactive precursor fraction for THMs formation. The ozonation process was also independently evaluated for its ability to remove the NOM fractions from water. Ozonation was found not to be very effective at NOM removal since it only resulted in a 12% overall decrease of the NOM in the water samples. The CD polyurethanes, when used alone, were also not very effective at removing the NOM fractions from water (maximum of 33% NOM removal). On the other hand, the combination method (i.e. the use of CD polyurethanes and ozonation for NOM removal) resulted in a good capability of the CD polyurethanes at decreasing some NOM fractions in water as evidenced by a 73% and 88% decrease of the HpiB and hydrophilic acid (HpiA) fractions, respectively. The 73% reduction of the HpiB fraction demonstrates a great success of the combination approach employed herein, as this study reports this fraction as the most reactive precursor fraction for THM formation.

M.Tech. (Biotechnology) / Please refer to full text to view abstract