Ethanol is used as fuel in neat form in some countries (Brazil and India) or blended with gasoline (Europe, Canada and the United States). The benefits of ethanol use include octane enhancement, a cleaner environment and a secure renewable energy supply. BTEX compounds (benzene, toluene, ethylbenzene, m-xylene, p-xylene and o-xylene) are aromatic hydrocarbons present in gasoline. The fate of these compounds in the environment is of great health concern due to their carcinogenic (benzene) and toxic properties, and due to their high solubility in water compared to the other gasoline hydrocarbons. Ethanol present in gasoline may affect BTEX degradation, in an event of a spill into the subsurface environment. To address the effects of ethanol on subsurface microorganisms, microbial activity and growth in the presence of ethanol (concentrations ranging 0 to 70% v/v) were assessed. Microcosms studies showed that ethanol at concentration ranging 0. 5 to3% (v/v) enhanced microbial activity and did not interfere inmicrobial growth at 10oC temperature, when another source of carbon was present (glucose). Ethanol at 0. 5% concentration enhanced microbial activity over water soluble gasoline components and R2A medium combined. Both microbialactivity and growth were not detected at ethanol concentrations equal and above 5%. Biodegradation study was conducted, in which subsurface material and ground water were exposed to BTEX and ethanol at 0. 5 and 1. 5% (v/v) concentration. The controls had BTEX alone and ethanol alone, sterile and nutrient-free. Total BTEX degradation was observed whenever ethanol was absent. Ethanol and BTEX were simultaneously degraded, however in microcosms containing 0. 5% ethanol, BTEX degradation was slowed, compared to microcosms without ethanol. Competition for inorganic nutrients was the major problem in slowed BTEX degradation in the presence of ethanol. In microcosms where 1. 5% ethanol was present, BTEX compounds and ethanol degradation were not observed.

Ethanol can affect the biodegradation of gasoline hydrocarbons in groundwater. High concentrations of ethanol can be toxic to subsurface microorganisms that are otherwise capable of degrading hydrocarbons, such as benzene, toluene, ethylbenzene and xylenes (BTEX). At lower concentrations, ethanol may hinder BTEX degradation through substrate competition and the depletion of inorganic nutrients (e.g., nitrogen and phosphorus), oxygen and other electron acceptors needed for BTEX degradation. A series of laboratory experiments were designed to study the effect of ethanol on aquifer microorganisms and on aerobic BTEX biodegradation. A microcosm experiment was conducted to investigate the effect of ethanol on the biodegradation of BTEX. Microcosms were set up with Borden aquifer material and groundwater in which oxygen and nutrients were not limited. These microcosms contained BTEX in combination with a range of ethanol concentrations. Under these favourable conditions, the presence of ethanol up to concentrations of 1.9% (v/v) (equivalent to 15000 mg/L) caused little inhibition of BTEX degradation. Further experiments were conducted to study the antimicrobial effects of higher concentrations of ethanol. Following exposure to ethanol concentrations of 25% (v/v) or higher, microbial activity and survival was significantly diminished. Results suggest that a high concentration ethanol slug will have a major impact on the microbial community but that there would likely be potential for recovery. The recovery potential was examined further in laboratory column experiments designed to simulate a dynamic field situation where a high ethanol pulse is followed by a BTEX plume. These column experiments were conducted with Borden aquifer material and groundwater under aerobic conditions. The concentration of the ethanol pulse was 25% (v/v), which was expected to significantly alter the microbial population without destroying it. Following the ethanol exposure, groundwater and BTEX were allowed to flow through one column to simulate the reinoculation of microorganisms from upgradient groundwater advecting into the contaminated zone. The other column was fed with sterile groundwater and BTEX to evaluate the regeneration of within-column microorganisms that survived the ethanol exposure. Recovery in both columns was rapid. Unfortunately, during the recovery phase, sterility of the influent groundwater could not be maintained. As a result, recovery by regeneration could not be evaluated. Nonetheless, it is evident that recovery in terms of aerobic BTEX biodegradation was significant under the conditions of the column experiment. Ethanol did not appear to pose a long-term impact on BTEX biodegradation when oxygen and nutrients were in excess. In field situations, nutrients and electron acceptors may be limited; however, ethanol toxicity is not likely to cause a prolonged inhibition of BTEX biodegradation.

Accidental spills of hydrocarbons from underground storage tanks or pipelines are a common cause of subsurface contamination. Anthropogenic hydrocarbon contamination of soil is a global issue throughout the industrialised world. In England and Wales alone, 12% of all serious contamination incidents in 2007 were hydrocarbon related. Biodegradation could be in situ process leading to a decrease of benzene concentrations in groundwater. Recently, monitored natural attenuation has become an effective alternative to the more active remediation methods for the in situ treatment of contaminated subsurface environments. The main objective of this study was to examine the possibility of adopting monitored natural attenuation as a remediation technique for the contaminated groundwater aquifer. In this natural attenuation study, the following tasks were conducted bioremediation investigation, biological first-order decay rates, Mann-Kendall Test model and BIOSCREEN model for the contaminated groundwater aquifer. In this study, a full-scale natural bioremediation investigation was conducted at a petroleum hydrocarbon spill site. In this study, The calculated biodegradation capacity (8.261 mg/L) at this site is much higher than the detected concentrations of petroleum-hydrocarbons (3-4 mg/L) within the most contaminated area inside the plume. Thus, natural biodegradation should be able to remove the contaminants effectively. The calculated biological first-order decay rates for benzene were between 1.7¡Ñ10-3-9.0¡Ñ10-4 day-1 respectively. Mann-Kendall test was applied to analyze the trend of contaminant variations. Results show that the S-value of monitor wells SW-1W, SW-4W, SW-42W, SW-23W, SW-30W, SW-67W and SW-70W were -2.23607, -1.16276, -1.52053, -1.34164, -1.26323, 0 and -1.34164, respectively. The negative S values reveal that the all contaminants tended to decrease. This indicates that the hydrocarbon plume at this site is not expanding, and has been contained effectively by the natural attenuation mechanisms. BIOSCREEN model from the groundwater analyses indicate, a first-order decay model reached the downgradient monitor well located 220 m from the spill location. that approximately 89% of the contaminate removal was due to biodegradation processes. The study of petroleum-hydrocarbons bacterial consortium were include Aquincola tertiaricarbonis L10¡BBosea sp. GR060219¡BBrachymonas petroleovorans strain CHX¡BHydrogenophaga sp. p3(2011)¡BHydrogenophaga sp.¡BMethylibium sp. YIM 61602¡BMycobacterium sp.¡BRhodoferax sp. IMCC1723¡BRhodoferax sp.¡BUncultured Rhodocyclaceae bacterium clone Elev_16S_975¡BUncultured Rhodocyclaceae bacterium clone eub62B1¤ÎUncultured Beggiatoa sp. clone GE7GXPU01BJTWR. Thus, the in situ bioremediation technology has the potential to be developed into an environmentally, economically and naturally acceptable remediation technology. Evidences for the occurrence of natural attenuation include the following: (1) depletion of dissolved oxygen, nitrate, and sulfate; (2) production of dissolved ferrous iron, sulfide, and CO2; (3) decreased BTEX concentrations and BTEX as carbon to TOC ratio along the transport path; (4) increased alkalinity and microbial species; (5) limited spreading of the BTEX plume; and (6) preferential removal of certain BTEX components along the transport path. Results indicate that natural attenuation can effectively contain the plume, and biodegradation processes played an important role on contaminant removal.

Contamination of groundwater by petroleum-hydrocarbons is a serious environmental problem. Monitored natural attenuation (MNA) is a passive remedial approach to degrade and dissipate contaminants in groundwater. In this study, a full-scale natural bioremediation investigation was conducted at a gasoline spill site. Results show that the concentrations of major contaminants [benzene, toluene, ethylbenzene, and xylenes (BTEX)] dropped to below detection limit before they reached the downgradient monitor well. This indicates that natural biodegradation process was the major cause of the contaminant reduction. In this study, 1,2,4-trimethylbenzene (1,2,4-TMB) was used as tracer to calculate the biological decay rates of BTEX. The calculated biological first-order decay rates for ethylbenzene, m+p-xylene, toluene, benzene, and o-xylene were 1.5¡Ñ10-3, 1.2¡Ñ10-3, 7.0¡Ñ10-4, 6.7¡Ñ10-4, and 1.2¡Ñ10-4, respectively. Mann-Kendall test was applied to analyze the trend of contaminant variations. Results show that the S-value of four monitor wells (CT-4, CT-41, CT-42, and CT-7) were -0.52, -1.57, -0.52, and -1.22, respectively. The negative S values reveal that the all contaminants tended to decrease. This indicates that the hydrocarbon plume at this site is not expanding, and has been contained effectively by the natural attenuation mechanisms. Evidences for the occurrence of natural attenuation include the following: (1) depletion of dissolved oxygen, nitrate, and sulfate; (2) production of dissolved ferrous iron, sulfide, and CO2; (3) decreased BTEX concentrations and BTEX as carbon to TOC ratio along the transport path; (4) increased alkalinity and microbial species; (5) limited spreading of the BTEX plume; and (6) preferential removal of certain BTEX components along the transport path. Results also show that the biodegradation capacity (46.02 mg/L) for BTEX and 1,2,4-TMB was much higher than the detected contaminants within the plume. Results indicate that natural attenuation can effectively contain the plume, and biodegradation processes played an important role on contaminant removal.

No description available.

Volatile organic compounds (VOCs) are emitted into the atmosphere from biogenic and anthropogenic sources with atmospheric lifetimes ranging from minutes to months, depending on the specific VOC compound considered. It is estimated that biogenic VOCs (BVOCs) (e.g. isoprenes, terpenes) make up 90% of the global atmospheric VOC budget. However, in highly industrialised regions, anthropogenic VOCs (e.g. benzene, toluene, ethylbenzene and xylene, combined abbreviated as BTEX) might dominate. VOCs have various reversible and irreversible effects on human health. They also have environmental impacts that range from changes in the population of terrestrial and aquatic ecosystems to the extinction of vulnerable species. VOCs are precursors for the formation of ozone (O3) during solar radiation initiated reactions in the presence of NOx. Tropospheric O3 is considered a pollutant, with negative impacts on human health, ecosystems and food security. O3 is also a short-lived greenhouse gas. Through reactions with radical species, VOCs lead to the formation of higher molecular weight organic compounds, which produce carbon monoxide (CO), peroxyacytyl nitrate (PAN) and ultimately secondary organic aerosol (SOA) particles. SOA particles impact directly on air quality and visibility, as well as directly and indirectly on the radiation balance of the earth that contributes to the regulation of climate. Notwithstanding the importance of atmospheric VOCs, limited data is available for VOCs in South Africa. In this study, a comprehensive dataset of BVOC and anthropogenic VOC species was obtained at the Welgegund measurement station in the North West Province, South Africa. Measurements were conducted from 9 February 2011 to 4 February 2012. Samples were collected on Tenax-TA and Carbopack-B adsorption tubes twice a week for two hours during day time and two hours during night time. The first 1.25m of the stainless steel sampling inlet was heated to 120ºC to remove O3 that could lead to sample degradation. Analyses of the sampled adsorption tubes were conducted by thermal desorption, cryofocusing, re-desorption, followed by gas chromatography separation and analysis with a mass selective detector (GC-MS). The results indicated that toluene was the most abundant aromatic hydrocarbon and heptane the most abundant alkane. Benzene is currently the only VOC listed as a criteria pollutant in the South African Air Quality Act with an annual average standard of 1.6ppb. The annual median benzene concentration was 0.13 ppb, while the highest daily benzene concentration measured was 8.7 ppb. No distinct seasonal cycles were identified for anthropogenic VOC species measured, i.e. aromatic hydrocarbons and alkanes. However, air mass history analysis indicated that air masses that passed over the Mpumalanga Highveld, the Vaal Triangle and the Johannesburg-Pretoria conurbation (collectively referred to as Area I) had significantly higher concentrations of these anthropogenic VOCs compared to air masses that passed over the western and eastern Bushveld Igneous Complex, and a region over which air masses typically followed an anti-cyclonic movement pattern (collectively referred to as Area II). Anthropogenic VOC levels in air masses that passed over the regional background (areas with no large point sources) had levels similar to air masses that had passed over Area II. Relatively good interspecies correlations (r > 0.8) between most of the aromatic hydrocarbons in air masses that had passed over Area I, with the exception of benzene, indicated that these species had common sources. Benzene, however, correlated well with CO, indicating that sources associated with incomplete combustion were most likely the origin of benzene in air masses that had passed over Area I. The interspecies concentration ratios for plumes passing over Area I indicated that this source region is relatively close to the Welgegund monitoring station and air masses that passed over this source region were substantially influenced by anthropogenic activities. The concentration ratios for plumes that passed over Area II and the Regional Background indicated that these were aged air masses. Furthermore, the concentration ratios of toluene, ethylbenzene and o,m,p-xylene (TEX) to the total aromatic concentration for air masses that passed over the various source regions showed a greater contribution to the total VOC concentration during periods of higher temperature, i.e. summer. This proved that the evaporation of solvents contributes significantly to VOC levels during the months with higher temperatures. The relative contribution of aromatic hydrocarbons to photochemical O3 formation in air masses that passed over the various source regions indicated the highest contribution was observed for air masses that passed over Area I, with Area II and the Regional Background in the same order of magnitude. The annual temporal variations of the measured BVOCs indicated that 2-methyl-3-buten-2-ol (MBO) and isoprene exhibited distinct seasonal patterns, i.e. higher values in summer and lower values in winter. The monoterpenes (MT) and the sesquiterpenes (SQT) did not follow distinct seasonal patterns. BVOC concentrations correlated relatively well to seasonal variations in temperature, photosynthetically active radiation (PAR), rainfall, relative humidity (RH) and CO2 flux. This proved that biogenic activity is responsible for BVOCs emitted. The most abundant MT was -pinene, while -caryophyllene was the most abundant SQT with annual median concentrations of 0.468 ppb and 0.022 ppb, respectively. Pollution roses for isoprene showed a dominance of sources from the north-west to the north-east, as well as the south-east. These directions correlated to areas where pockets of the savannah biome are located. / Thesis (MSc (Environmental Sciences))--North-West University, Potchefstroom Campus, 2013

Volatile organic compounds (VOCs) are emitted into the atmosphere from biogenic and anthropogenic sources with atmospheric lifetimes ranging from minutes to months, depending on the specific VOC compound considered. It is estimated that biogenic VOCs (BVOCs) (e.g. isoprenes, terpenes) make up 90% of the global atmospheric VOC budget. However, in highly industrialised regions, anthropogenic VOCs (e.g. benzene, toluene, ethylbenzene and xylene, combined abbreviated as BTEX) might dominate. VOCs have various reversible and irreversible effects on human health. They also have environmental impacts that range from changes in the population of terrestrial and aquatic ecosystems to the extinction of vulnerable species. VOCs are precursors for the formation of ozone (O3) during solar radiation initiated reactions in the presence of NOx. Tropospheric O3 is considered a pollutant, with negative impacts on human health, ecosystems and food security. O3 is also a short-lived greenhouse gas. Through reactions with radical species, VOCs lead to the formation of higher molecular weight organic compounds, which produce carbon monoxide (CO), peroxyacytyl nitrate (PAN) and ultimately secondary organic aerosol (SOA) particles. SOA particles impact directly on air quality and visibility, as well as directly and indirectly on the radiation balance of the earth that contributes to the regulation of climate. Notwithstanding the importance of atmospheric VOCs, limited data is available for VOCs in South Africa. In this study, a comprehensive dataset of BVOC and anthropogenic VOC species was obtained at the Welgegund measurement station in the North West Province, South Africa. Measurements were conducted from 9 February 2011 to 4 February 2012. Samples were collected on Tenax-TA and Carbopack-B adsorption tubes twice a week for two hours during day time and two hours during night time. The first 1.25m of the stainless steel sampling inlet was heated to 120ºC to remove O3 that could lead to sample degradation. Analyses of the sampled adsorption tubes were conducted by thermal desorption, cryofocusing, re-desorption, followed by gas chromatography separation and analysis with a mass selective detector (GC-MS). The results indicated that toluene was the most abundant aromatic hydrocarbon and heptane the most abundant alkane. Benzene is currently the only VOC listed as a criteria pollutant in the South African Air Quality Act with an annual average standard of 1.6ppb. The annual median benzene concentration was 0.13 ppb, while the highest daily benzene concentration measured was 8.7 ppb. No distinct seasonal cycles were identified for anthropogenic VOC species measured, i.e. aromatic hydrocarbons and alkanes. However, air mass history analysis indicated that air masses that passed over the Mpumalanga Highveld, the Vaal Triangle and the Johannesburg-Pretoria conurbation (collectively referred to as Area I) had significantly higher concentrations of these anthropogenic VOCs compared to air masses that passed over the western and eastern Bushveld Igneous Complex, and a region over which air masses typically followed an anti-cyclonic movement pattern (collectively referred to as Area II). Anthropogenic VOC levels in air masses that passed over the regional background (areas with no large point sources) had levels similar to air masses that had passed over Area II. Relatively good interspecies correlations (r > 0.8) between most of the aromatic hydrocarbons in air masses that had passed over Area I, with the exception of benzene, indicated that these species had common sources. Benzene, however, correlated well with CO, indicating that sources associated with incomplete combustion were most likely the origin of benzene in air masses that had passed over Area I. The interspecies concentration ratios for plumes passing over Area I indicated that this source region is relatively close to the Welgegund monitoring station and air masses that passed over this source region were substantially influenced by anthropogenic activities. The concentration ratios for plumes that passed over Area II and the Regional Background indicated that these were aged air masses. Furthermore, the concentration ratios of toluene, ethylbenzene and o,m,p-xylene (TEX) to the total aromatic concentration for air masses that passed over the various source regions showed a greater contribution to the total VOC concentration during periods of higher temperature, i.e. summer. This proved that the evaporation of solvents contributes significantly to VOC levels during the months with higher temperatures. The relative contribution of aromatic hydrocarbons to photochemical O3 formation in air masses that passed over the various source regions indicated the highest contribution was observed for air masses that passed over Area I, with Area II and the Regional Background in the same order of magnitude. The annual temporal variations of the measured BVOCs indicated that 2-methyl-3-buten-2-ol (MBO) and isoprene exhibited distinct seasonal patterns, i.e. higher values in summer and lower values in winter. The monoterpenes (MT) and the sesquiterpenes (SQT) did not follow distinct seasonal patterns. BVOC concentrations correlated relatively well to seasonal variations in temperature, photosynthetically active radiation (PAR), rainfall, relative humidity (RH) and CO2 flux. This proved that biogenic activity is responsible for BVOCs emitted. The most abundant MT was -pinene, while -caryophyllene was the most abundant SQT with annual median concentrations of 0.468 ppb and 0.022 ppb, respectively. Pollution roses for isoprene showed a dominance of sources from the north-west to the north-east, as well as the south-east. These directions correlated to areas where pockets of the savannah biome are located. / Thesis (MSc (Environmental Sciences))--North-West University, Potchefstroom Campus, 2013

Submitted by Gisele Mara Hadlich (gisele@ufba.br) on 2017-11-30T14:11:07Z No. of bitstreams: 1 DISSERTAÇÃO - PAULA.pdf: 4642516 bytes, checksum: 80a02cde7041f02a85b3b3204fffda61 (MD5) / Made available in DSpace on 2017-11-30T14:11:07Z (GMT). No. of bitstreams: 1 DISSERTAÇÃO - PAULA.pdf: 4642516 bytes, checksum: 80a02cde7041f02a85b3b3204fffda61 (MD5) / Com o objetivo de se determinar os compostos voláteis BTEX em águas subterrâneas de postos de gasolina, foi implantado o método de determinação de compostos voláteis por purge and trap e espectrometria de cromatografia de massa (GC-MS), EPA 8260C e 5030C. A validação do método foi realizada através do estudo de seletividade, linearidade, sensibilidade, exatidão, precisão, limite de detecção (LD), limite de quantificação (LQ) e robustez. A curva de calibração varia de 2 a 200 μg.L-1, com valores de recuperação dentro de um intervalo 70 a 120%, com precisão de 20%. Para se investigar a contaminação do aquífero da bacia do Rio Lucaia, Salvador, Bahia, por compostos derivados de petróleo devido a vazamentos de tanques combustíveis, foi determinada em amostras de águas subterrâneas, as concentrações de benzeno, tolueno, etilbenzeno e xilenos (BTEX), sulfato nitrato e ferro (II). A concentração de BTEX variou de 0,2-185,7 µg/L nas águas subterrâneas e as concentrações de sulfato, nitrato e ferro (II) foram correlacionados com os níveis de BTEX e sua degradação natural. Apenas em dois pontos foram observados os níveis de BTEX muito acima do permitido pelo CONAMA, as outras foram abaixo do LD ou não foram detectadas. Uma segunda coleta foi realizada, verificando-se a redução do teor de BTEX nos pontos amostrais da Bacia do rio Lucaia em até 82%. Os valores de nitrato, sulfato e ferro (II) foram relacionados nas duas campanhas observando-se a provável degradação natural dos compostos tendo como aceptores preferenciais o nitrato e o ferro (III), bem como a não dispersão da contaminação em níveis críticos para a população. O trabalho apresentado faz parte do projeto “Contaminação de Águas Subterrâneas por Derivados de Petróleo e Etanol oriundos de Postos de Distribuição na Região Metropolitana de Salvador: Subsídios para a Remediação Ambiental.” Aprovado no Edital 05/2007 pelo termo de outorga FAPESB – UFBA nº 8657 sobre os auspício do Núcleo de Estudos Ambientais do Instituto de Geociências da Universidade Federal da Bahia.

This study aims to determine the contribution of evaporative emissions from light passenger vehicles to the degradation of the air quality. The main objective is to evaluate the concentrations volatile monoaromatic compounds benzene, toluene, ethylbenzene and xylenes (BTEX) indoors, in a site that represents the reality of the vehicular fleet of the Metropolitan Region of Rio de Janeiro. The samples were collected in an underground parking lot of a shopping mall in the northern zone of Rio de Janeiro, by a system of active sampling using charcoal cartridge as the adsorbent. The samples were extracted with organic solvent and subsequently analyzed by gas chromatography-mass spectrometry (GCMS). The average results were 52.7 μg.m-3 for benzene, toluene to 203.6 μg.m-3, 44.6 μg.m-3 for ethylbenzene, 115.7 μg.m-3 for xylene, toluene and the compound found in majority. These results were compared with results from the literature of vehicular emissions in confined spaces such as garages and tunnels. We investigated the correlation with emissions from a moving vehicle, obtained from previous studies in a tunnel of large circulation and emissions obtained in the underground parking. The results demonstrate demonstrated different emission sources. / Este trabalho visa determinar a contribuição das emissões evaporativas provenientes dos veículos leves de passageiro, para a degradação da qualidade do ar atmosférico. O objetivo principal é avaliar as concentrações compostos monoaromáticos voláteis Benzeno, Tolueno, Etilbenzeno e Xilenos (BTEX) em ambientes confinados, sendo este realizado em um local que caracterize a realidade da frota veicular da Região metropolitana do Rio de Janeiro. As amostras foram coletadas em um estacionamento subterrâneo de um Shopping Center da zona norte do Rio de Janeiro, através do sistema de amostragem ativa, utilizando cartucho de carvão ativo como adsorvente. As amostras foram extraídas com solvente orgânico e analisadas posteriormente por Cromatografia gasosa acoplada à espectrometria de massas (CGEM). As médias dos resultados obtidos foram 52,7 g.m-3 para o benzeno, 203,6 g.m-3 para o tolueno, 44,6 g.m-3 para o etilbenzeno, 115,7 g.m-3 para os xilenos, sendo o tolueno o composto encontrado em maior abundância. Esses resultados foram comparados com resultados encontrados na literatura de emissões veiculares em ambientes confinados como garagens e túneis. Foi investigada a correlação com as emissões do veículo em movimento, obtidas através de estudos previamente realizados em um túnel de grande circulação e as emissões obtidas no estacionamento subterrâneo. Através desses dados ficou demonstrada diferença das fontes de emissão.

The performance of a submerged membrane bioreactor for the duty of gas field produced water treatment was appraised. The system was operated under steady state conditions at a range of mixed liquor suspended solids (MLSS) concentrations and treatment and membrane performance examined. Organics removal (COD and TOC) display removal rates between 90 and 97%. Removal of specific target compounds Benzene, Toulene, Ethylbenzene and Xylene were removed to above 99% in liquid phase with loss to atmosphere between 0.3 and 1%. Comparison of fouling rates at a number of imposed fluxes has been made between long term filtration trials and short term tests using the flux step method. Produced water fed biomass displays a greater fouling propensity than municipal wastewater fed biomass from previous studies. Results indicate an exponential relationship between fouling rate and flux for both long and short term trials, although the value was an order of magnitude lower during long term tests. Moreover, operation during long term trials is characterised by a period of pseudo stable operation followed by a catastrophic rise in TMP at a given critical filtration time (tfi, ) during trials at 6 g. L"1. This time of stable operation, tfit, is characterised by a linear relationship between fouling rate and flux. Results have been compared with the literature. Data for membrane fouling prior to the end of t fit yielded a poor fit with a recently proposed model. Trends recorded at t> trlt revealed the fouling rate to follow no definable trend with flux. The system showed resilience to free oil shocking up to an oil concentration of 200ppmv. Following an increase in oil concentration to 500 ppmv, rapid and exponential fouling ensued.