Hadi M. A. Abood
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Hadi M. A. Abood has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
D.H. Kerridge
3 shared publications- Andrew P. Abbott
University of Leicester
2 shared publications - Karl Scott Ryder
University of Leicester
2 shared publications - Andrew D. Ballantyne
Chemistry Department, University of Leicester, Leicester, UK
1 shared publication Bassam B. Hasan
1 shared publicationFulian Qiu
Department of Chemistry, University of Leicester, Leicester, UK
1 shared publication
Latest Publications
- 8 February 2011
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 47 (12) , 3523-3525
Do all ionic liquids need organic cations? Characterisation of [AlCl2·nAmide]+ AlCl4− and comparison with imidazolium based systems
The addition of a simple amide to AlCl3 causes the formation of a liquid of the form [AlCl2·nAmide]+AlCl4 −. The material thus produced is liquid over a wide temperature range, is relatively insensitive to water and has the properties of an ionic liquid. This ionic liquid is shown to be a suitable medium for the acetylation of ferrocene and the electrodeposition of aluminium and demonstrated that quaternary ammonium cations are not always needed to form ionic liquids.
- 8 February 2011
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 47 (12) , 3523-3525
Do all ionic liquids need organic cations? Characterisation of [AlCl2·nAmide]+ AlCl4− and comparison with imidazolium based systems
The addition of a simple amide to AlCl3 causes the formation of a liquid of the form [AlCl2·nAmide]+AlCl4 −. The material thus produced is liquid over a wide temperature range, is relatively insensitive to water and has the properties of an ionic liquid. This ionic liquid is shown to be a suitable medium for the acetylation of ferrocene and the electrodeposition of aluminium and demonstrated that quaternary ammonium cations are not always needed to form ionic liquids.
- 18 November 2009
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 12 (8) , 1862-1872
Double layer, diluent and anode effects upon the electrodeposition of aluminium from chloroaluminate based ionic liquids
The deposition of aluminium from a chloroaluminate based ionic liquid was studied to elucidate the effect of a diluent (toluene) and electrolyte (LiCl) on the deposit morphology. A wide variety of analytical techniques was applied to this system to determine the speciation and mechanism of material growth. These included: 27Al NMR, FAB-MS, cyclic voltammetry, chronocoulometry, chronopotentiometry, scanning electron microscopy and atomic force microscopy. It was found that under-potential deposition (upd) causes a change in the way in which metal grows on the electrode surface. Metal grows in two regimes which are believed to be nano-material and bulk material. The addition of toluene causes a change in speciation and a decrease in upd which in turn changes the morphology of the deposit obtained and can lead to mirror finish aluminium. The addition of LiCl has the opposite effect encouraging upd and leading to larger crystallites and a dark grey deposit. It is also shown for the first time that under many conditions the rate of the anodic dissolution process is overall rate controlling and one effect of the addition of toluene is to increase the rate of anodic dissolution.
- 18 November 2009
- Published by Royal Society of Chemistry (RSC) in Physical Chemistry Chemical Physics
- Vol. 12 (8) , 1862-1872
Double layer, diluent and anode effects upon the electrodeposition of aluminium from chloroaluminate based ionic liquids
The deposition of aluminium from a chloroaluminate based ionic liquid was studied to elucidate the effect of a diluent (toluene) and electrolyte (LiCl) on the deposit morphology. A wide variety of analytical techniques was applied to this system to determine the speciation and mechanism of material growth. These included: 27Al NMR, FAB-MS, cyclic voltammetry, chronocoulometry, chronopotentiometry, scanning electron microscopy and atomic force microscopy. It was found that under-potential deposition (upd) causes a change in the way in which metal grows on the electrode surface. Metal grows in two regimes which are believed to be nano-material and bulk material. The addition of toluene causes a change in speciation and a decrease in upd which in turn changes the morphology of the deposit obtained and can lead to mirror finish aluminium. The addition of LiCl has the opposite effect encouraging upd and leading to larger crystallites and a dark grey deposit. It is also shown for the first time that under many conditions the rate of the anodic dissolution process is overall rate controlling and one effect of the addition of toluene is to increase the rate of anodic dissolution.
- 1 February 1993
- Published by Elsevier in Thermochimica Acta
- Vol. 215, 183-188
Thermal stability and solubility of alkaline earth nitrates and chromates in nitrate melts
- 1 February 1993
- Published by Elsevier in Thermochimica Acta
- Vol. 215, 183-188
Thermal stability and solubility of alkaline earth nitrates and chromates in nitrate melts
- 30 April 1992
- Published by Elsevier in Thermochimica Acta
- Vol. 198 (2) , 297-302
The reaction of potassium iodide in molten nitrate eutectics
- 30 April 1992
- Published by Elsevier in Thermochimica Acta
- Vol. 198 (2) , 297-302
The reaction of potassium iodide in molten nitrate eutectics
- 21 August 1991
- Published by Elsevier in Thermochimica Acta
- Vol. 185 (1) , 35-49
Thermogravimetric studies of the catalytic activity of molten alkali metal sulphate solutions of vanadium and niobium
- 21 August 1991
- Published by Elsevier in Thermochimica Acta
- Vol. 185 (1) , 35-49
Thermogravimetric studies of the catalytic activity of molten alkali metal sulphate solutions of vanadium and niobium