https://ogma.newcastle.edu.au/vital/access/ /manager/Index en-au 5 Surface nanobubbles in nonaqueous media: looking for nanobubbles in DMSO, formamide, propylene carbonate, ethylammonium nitrate, and propylammonium nitrate https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:20313 Wed 28 Aug 2024 10:41:59 AEST ]]> Switchable long-range double layer force observed in a protic ionic liquid https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:33574 Wed 21 Nov 2018 14:49:32 AEDT ]]> Hofmeister effects influence bulk nanostructure in a protic ionic liquid https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:50877 Wed 16 Aug 2023 10:51:36 AEST ]]> Combined STM, AFM and DFT study of the HOPG / 1-octyl-3-methyl-imidazolium bis(trifluoromethylsulfonyl)amide ([OMIm]Tf2N) interface https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:14672 Wed 11 Apr 2018 16:24:54 AEST ]]> Mechanistic aspects of molecular imprinting by precipitation polymerisation https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:31445 Wed 11 Apr 2018 14:55:03 AEST ]]> Self-assembly and structure in ionic liquids and their mixtures https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:22987 Wed 11 Apr 2018 10:54:18 AEST ]]> Molecular structure, flow properties and particle stability and settling in protic ionic liquids https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:14442 Wed 11 Apr 2018 10:48:05 AEST ]]> Nanostructure of the H-terminated p-Si(111)/ionic liquid interface and the effect of added lithium salt https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:31333 1,4]TFSA). AFM measurements reveal that the imidazolium cation adsorbs at the H-Si(111)/[EMIm]TFSA interface leading to an ordered clustered facet structure of ∼3.8 nm in size. In comparison, the Si(111)/[Py1,4]TFSA interface appeared the same as the native surface in argon. For both pure ILs, repulsive forces were measured as the tip approached the surface. On addition of LiTFSA attractive forces were measured, revealing marked changes in the interfacial structure.]]> Wed 11 Apr 2018 09:55:10 AEST ]]> Ionic liquid lubrication : influence of ion structure, surface potential and sliding velocity https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:13680 − anion-enriched layer is more lubricating than either the [BMIM]+ or FAP- layers. The effect of cation charged group (charge-delocalised versus charged-localised) was investigated by comparing [BMIM] FAP with 1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl)trifluorophosphate ([Py] FAP). [BMIM] FAP is less lubricating at negative potentials, but more lubricating at positive potentials. This indicated that even at positive potentials the cation concentration in the boundary layer is sufficiently high to influence lubricity. The influence of sliding velocity on lateral force was investigated for the [EMIM] FAP–Au(111) system. At neutral potentials the behaviour is consistent with a discontinuous sliding process. When a positive or negative potential bias is applied, this effect is less pronounced as the colloid probe slides along a better defined ion plane.]]> Tue 13 Aug 2024 14:38:51 AEST ]]> Fundamental understanding of optimal methods of contacting ionic liquids and gases at high flow rates with a focus on capturing fugitive methane emissions from mining operations https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:56154 Thu 08 Aug 2024 14:45:17 AEST ]]> Comparative leaching of a sulfidic gold ore in ionic liquid and aqueous acid with thiourea and halides using Fe(III) or HSO₅⁻ oxidant https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:7233 Sat 24 Mar 2018 08:33:47 AEDT ]]> Cycling and rate performance of Li-LiFePO₄ cells in mixed FSI-TFSI room temperature ionic liquids https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:10246 Sat 24 Mar 2018 08:13:09 AEDT ]]> Metal-templated macrocycle synthesis in an ionic liquid: a comparison with reaction in protic solvents https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:19655 Sat 24 Mar 2018 08:01:13 AEDT ]]> Physicochemical interactions of ionic liquids with coal; the viability of ionic liquids for pre-treatments in coal liquefaction https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:27116 Sat 24 Mar 2018 07:41:36 AEDT ]]> Specific heat control of nanofluids: a critical review https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:26070 Sat 24 Mar 2018 07:31:30 AEDT ]]> Metal ion adsorption at the ionic liquid-mica interface https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:24137 3+ system, less obviously for the divalent ions and not at all for monovalent ions. This difference is attributed to the strength of electrostatic interactions between metal ions and mica charge sites increasing with the ion charge, which means that divalent and (particularly) trivalent ions are located more precisely above the charged sites of the mica lattice. The images obtained allow important distinctions between metal ion adsorption at mica-water and mica-PAN interfaces to be made.]]> Sat 24 Mar 2018 07:16:33 AEDT ]]> Combined nano- and macrotribology studies of titania lubrication using the oil-ionic liquid mixtures https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:23832 Sat 24 Mar 2018 07:12:13 AEDT ]]> High voltage carbon-based cathodes for non-aqueous aluminium-ion batteries** https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:40107 60 and C70 fullerene (CFEx) and Super-P carbon black were tested and compared as cathodes for non-aqueous aluminium-ion batteries (AIBs). These materials differ in their general structure, porosity and morphology. Fullerenes display a crystalline structure, whereas hemp fibers, Super-P and hair are amorphous in nature. Of all materials, AC obtained from hair recorded the highest specific capacity after 50 cycles at 103 mAh g−1 with a Coulombic efficiency of ∼90 % at a current rate of 50 mA g−1. Both hemp fibers and Super-P achieved their highest specific capacities at 56 mAh g−1 and 84 mAh g−1 respectively. CFEx recorded its highest capacity at 78 mAh g−1 and maintained it for 50 cycles. The cells were charged and discharged to 2.45 V and 0.2 V respectively.]]> Mon 29 Jan 2024 17:43:46 AEDT ]]> In situ scanning tunneling microscopy (STM), atomic force microscopy (AFM) and quartz crystal microbalance (EQCM) studies of the electrochemical deposition of tantalum in two different ionic liquids with the 1-butyl-1-methylpyrrolidinium cation https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:22100 5 in two hydrophobic ionic liquids (1-butyl-1-methylpyrrolidinium tris(pentafluoroethyl) trifluorophosphate ([Py1,4]FAP) and 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl) amide ([Py1,4]TFSA) is probed using three in situ techniques: scanning tunneling microscopy (STM), atomic force microscopy (AFM), and electrochemical quartz crystal microbalance (EQCM). These techniques reveal that under similar conditions TaF5is more easily reduced in the liquids with [TFSA] than [FAP]anions. Increasing the temperature reduced the viscosity and density of the ionic liquids which facilitates TaF5 electroreduction, in particular, in [Py1,4]TFSA. A herringbone reconstruction of the Au electrode was observed by STM for both ionic liquids with and without TaF5. Ta deposition was proved by STM and EQCM in [Py1,4]TFSA. Cracked layers, with ionic liquid trapped inside, were obtained by direct plating from the [TFSA]− ionic liquid. No Ta containing deposits could be obtained in the liquid with the [FAP]− anion.]]> Mon 23 Sep 2019 11:13:11 AEST ]]> In situ scanning tunneling microscopy (STM), atomic force microscopy (AFM) and quartz crystal microbalance (EQCM) studies of the electrochemical deposition of tantalum in two different ionic liquids with the 1-butyl-1-methylpyrrolidinium cation https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:24002 in situ techniques: scanning tunneling microscopy (STM), atomic force microscopy (AFM), and electrochemical quartz crystal microbalance (EQCM). These techniques reveal that under similar conditions TaF₅ is more easily reduced in the liquids with [TFSA]⁻ than [FAP]-anions. Increasing the temperature reduced the viscosity and density of the ionic liquids which facilitates TaF₅ electroreduction, in particular, in [Py₁,₄]TFSA. A herringbone reconstruction of the Au electrode was observed by STM for both ionic liquids with and without TaF₅. Ta deposition was proved by STM and EQCM in [Py₁,₄]TFSA. Cracked layers, with ionic liquid trapped inside, were obtained by direct plating from the [TFSA]⁻ ionic liquid. No Ta containing deposits could be obtained in the liquid with the [FAP]⁻ anion.]]> Mon 23 Sep 2019 10:21:47 AEST ]]> Abatement of Greenhouse Gas Emissions from Ventilation Air Methane (VAM) Using Ionic Liquids: A Review of Experimental Methods and Modelling Approaches https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:51081 Fri 18 Aug 2023 09:32:00 AEST ]]> Is the boundary layer of an ionic liquid equally lubricating at higher temperature? https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:24748 Fri 16 Aug 2024 16:22:32 AEST ]]>