https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Investigation of the reaction mechanism for reactive ground https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:52491 Wed 13 Mar 2024 13:56:53 AEDT ]]> Heterocoagulation of chalcopyrite and pyrite minerals in flotation separation https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:448 Thu 25 Jul 2013 09:09:49 AEST ]]> Electrochemical characterization of the interaction between ammonium nitrate and reactive ground https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:46146 4NO3 and FeS2, a major component of reactive ground. Voltammetric processes corresponding to the Fe(II)/Fe(III) redox couple and the reduction of nitrate are observed. This is significant as the existing reaction mechanism shows nitrate reacting in the electrolyte, but not being reduced on the surface of the FeS2. An irreversible oxidation occurs at ~0 V versus SCE associated with the re-oxidation of species formed at lower potentials. This is not associated with a change in the potential of the electrolyte, indicating a surface reaction. With the use of thermocouples, an exothermic reaction above 0.4 V is observed. FeS2 is initially unreactive in NH4NO3 solutions. After FeS2 exposure to potentials above 0.6 V versus SCE, the material becomes active and catalytic in nature. Material reacted following the industry standard Australian Explosives Industry Safety Group (AEISG) test method shows similar catalytic behaviour in the presence of fresh NH4NO3. This is significant for the safety and testing of reactive ground, as even FeS2 that has completed reaction still has the potential to undergo further reaction if introduced to fresh NH4NO3.]]> Fri 11 Nov 2022 18:30:55 AEDT ]]> Oxidative transformation of iron monosulfides and pyrite in estuarine sediments: implications for trace metals mobilisation https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:33161 Fri 07 Sep 2018 16:40:17 AEST ]]>