Brian O’Neill
University of Adelaide
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Publication
Featured researches published by Brian O’Neill.
Journal of Hazardous Materials | 2011
Mike B. Dixon; Yann Richard; Lionel Ho; Christopher W.K. Chow; Brian O’Neill; Gayle Newcombe
Cyanobacteria are a major problem for the world wide water industry as they can produce metabolites toxic to humans in addition to taste and odour compounds that make drinking water aesthetically displeasing. Removal of cyanobacterial toxins from drinking water is important to avoid serious illness in consumers. This objective can be confidently achieved through the application of the multiple barrier approach to drinking water quality and safety. In this study the use of a multiple barrier approach incorporating coagulation, powdered activated carbon (PAC) and ultrafiltration (UF) was investigated for the removal of intracellular and extracellular cyanobacterial toxins from two naturally occurring blooms in South Australia. Also investigated was the impact of these treatments on the UF flux. In this multibarrier approach, coagulation was used to remove the cells and thus the intracellular toxin while PAC was used for extracellular toxin adsorption and finally the UF was used for floc, PAC and cell removal. Cyanobacterial cells were completely removed using the UF membrane alone and when used in conjunction with coagulation. Extracellular toxins were removed to varying degrees by PAC addition. UF flux deteriorated dramatically during a trial with a very high cell concentration; however, the flux was improved by coagulation and PAC addition.
American Mineralogist | 2006
Haipeng Wang; Allan Pring; Yung Ngothai; Brian O’Neill
Abstract The kinetic behavior of the α-Ni1-xS → β-NiS transition was investigated via a series of annealquench experiments using Rietveld quantitative phase analysis of powder X-ray diffraction data. Initial compositions of α-Ni1-xS were found to play an important role in the kinetics of the transition. The activation energy (Ea) for this α- to β-phase transition is 16.0 (±0.5) kJ/mol for NiS in the temperature range 343 to 423 K, and 13.0 (±0.5) kJ/mol in the temperature range 523 to 623 K. For Ni0.97S, however, Ea decreases from 73.0 (±0.5) to 17.0 (±0.5) kJ/mol over the course of the reaction in the temperature range 573 to 593 K. The relationship between Ea and extent of transition (y) for the initial bulk Ni0.97S was derived using the Refined Avrami method. For Ni-deficient compositions, α-Ni1-xS, the transformation to β-NiS is accompanied by the exsolution of a progressively more Ni-deficient α-Ni1-xS and Ni3S4, and the reactions become more sluggish for more metal-deficient compositions.
Colloids and Surfaces B: Biointerfaces | 2012
Fan Wu; Yung Ngothai; Jie Wei; Changsheng Liu; Brian O’Neill; Yuequn Wu
By using a non-aqueous solution as the mixing liquid, the washout resistance of the calcium deficient apatite biocement (cd-AB) was significantly improved, over that of the conventional method of using cd-AB with water as the liquid phase. In this study, premixed and injectable cd-AB was prepared, which had the advantage of being stable in the syringe and hardens only after being delivered to the defect area. The cd-AB powder with a Ca/P ratio of 1.5 consists of a mixture of tetracalcium phosphate (TTCP) and dicalcium phosphate anhydrous (DCPA). A solution of polylactide (PLA) in N-methyl-2-pyrrolidone (NMP) was used as the liquid phase of the premixed cd-AB. The premixed cd-AB paste injected into an aqueous environment exhibited excellent washout resistance. The premixed cd-AB had longer setting time and lower compressive strength than conventional cd-AB. The hydration products of premixed cd-AB were a mixture of calcium deficient hydroxyapatite (cd-HA) and PLA. In vitro Tris-HCl immersion tests demonstrated that the premixed cd-AB could be degradable. The results revealed that the premixed cd-AB was cytocompatible and had no adverse effects on the attachment and proliferation of MG-63 osteoblast-like cells in vitro. The most distinct advantages of premixed and injectable PLA-modified cd-AB were its excellent washout resistance and in vitro degradability, suggesting that it may be a promising candidate for bone repair.
American Mineralogist | 2015
Kan Li; Allan Pring; Barbara Etschmann; Edeltraud Macmillan; Yung Ngothai; Brian O’Neill; Anthony Hooker; Fred Mosselmans; Joël Brugger
Abstract Interface coupled dissolution-reprecipitation reactions (ICDR) are a common feature of fluid-rock interaction during crustal fluid flow. We tested the hypothesis that ICDR reactions can play a key role in scavenging minor elements by exploring the fate of U during the experimental sulfidation of hematite to chalcopyrite under hydrothermal conditions (220-300 °C). The experiments where U was added, either as solid UO2+x(s) or as a soluble uranyl complex, differed from the U-free experiments in that pyrite precipitated initially, before the onset of chalcopyrite precipitation. In addition, in UO2+x(s)- bearing experiments, enhanced hematite dissolution led to increased porosity and precipitation of pyrite+magnetite within the hematite core, whereas in uranyl nitrate-bearing experiments, abundant pyrite formed initially, before being replaced by chalcopyrite. Uranium scavenging was mainly associated with the early reaction stage (pyrite precipitation), resulting in a thin U-rich line marking the original hematite grain surface. This “line” consists of nanocrystals of UO2+x(s), based on chemical mapping and XANES spectroscopy. This study shows that the presence of minor components can affect the pathway of ICDR reactions. Reactions between U- and Cu-bearing fluids and hematite can explain the Cu-U association prominent in some iron oxide-copper-gold (IOCG) deposits.
Food and Bioprocess Technology | 2016
Richard Muhlack; Brian O’Neill; Elizabeth J. Waters; C. Colby
Protein instability in white wine can result in unsightly haze formation, and therefore, its prevention by adsorption of haze proteins onto bentonite is an important unit operation in commercial wine production. Optimisation of this process is challenging due to the performance impact of environmental factors and matrix effects which are difficult to control and study in wine systems. These issues are addressed in the present study; the effect of different factors on adsorption behaviour of a purified thaumatin-like grape protein (VVTL1) by sodium bentonite in a chemically defined model wine solution was investigated using a factorial design with surface response analysis. Bentonite adsorption of VVTL1 was well characterised by a multi-factor Langmuir adsorption model. The main effects of pH, temperature, potassium concentration as well as the pH*potassium matrix interaction all had a significant effect (p < 0.05) on the adsorption capacity, as did the aging of bentonite slurry before use. Observations support the hypothesis that VVTL1 adsorption onto sodium bentonite is affected by steric mass action and local interactions of exposed protein charge, with pH and temperature effects related to changes in protein conformation under those conditions. Variation in potassium concentration can cause similar effects and influence adsorption capacity by affecting bentonite swelling and charge potential, providing a greater surface area for adsorption. From a processing perspective, results suggest bentonite treatment efficiency will be optimised by treating wines at higher temperatures rather than during cold storage, at the lower pH and before cold (tartrate) stabilisation.
Chemical Engineering Communications | 2017
Ali Mirsepahi; Lei Chen; Brian O’Neill
In order to check the applicability of Artificial Intelligent (AI) techniques to act as reliable inverse models to solve the multi-input/multi-output heat flux estimation classes of inverse heat transfer problems (IHTPs), in a newly reconstructed experimental setup, a two-input/two-two output (TITO) heat flux estimation problem was defined in which the radiation acts as the main mode of thermal energy. A simple three-layer perceptron Artificial Neural Network (ANN) was designed, trained, and employed to estimate the input powers (represent emitted heats-heat fluxes from two halogen lamps) to irradiative batch drying process. To this end, different input power functions (signals) were input to the furnace/dryer’s halogen lamps, and the resultant temperature histories were measured and recorded for two different points of the dryer/furnace. After determining the required parameters, the recorded data were prepared and arranged to be used for inverse modelling purposes. Next, an ANN was designed and trained to play the role of the inverse heat transfer model. The results showed that ANNs are applicable to solve heat flux estimation classes of IHTPs.
Geochimica et Cosmochimica Acta | 2009
Fang Xia; Joël Brugger; Guorong Chen; Yung Ngothai; Brian O’Neill; Andrew Putnis; Allan Pring
Radiation Physics and Chemistry | 2010
Joël Brugger; Allan Pring; Frank Reith; C.G. Ryan; Barbara Etschmann; Weihua Liu; Brian O’Neill; Yung Ngothai
Geochimica et Cosmochimica Acta | 2011
Blake Tooth; Cristiana L. Ciobanu; Leonard Green; Brian O’Neill; Joël Brugger
Crystal Growth & Design | 2009
Fang Xia; J. Brugger; Yung Ngothai; Brian O’Neill; Guorong Chen; Allan Pring