Aluminium solubility

The overriding aim of our research on HAS(j) is to elucidate their role in the biogeochemical cycle of aluminium [16] and specifically to understand how they keep aluminium out of biota [17]. This has led us to try to define a solubility expression for HASb(s) order that such might be used quantitatively in predictive models of aluminium solubility control in soil and surface waters [18]. The solubility constant which we derived from our unconventional solubility expression ... 

Gustafsson, J. P., D. G. Lumsdon, and M. Simonsson. 1998. Aluminium solubility characteristics of spodic B horizons containing imogolite-type materials. Clay Minerals 33, no. 1 77-86. 

The metallic aluminium solubility in cryolite-alumina melts decreases with the temperature decrease. Likewise this also decreases with the cryolite rate decrease. If it is supposed that these dependences are also available in the case of K3 AlFg melts, an increase of current efficiency will result in those melts. 

Andersen, S., Christophersen, N., Mulder, J., Seip, H.M. and R.D.Vogt (1990). Aluminium solubility in the various soil horizons in an acidified catchment. Surface Water Acidification Programme, Final Report, (J.Mason, ed.) The Royal Society, London, (in press). 

Conyers, M. (1990). The control of aluminium solubility in some acidic Australian soils. Journal of Soil Science, 41, 147-156. 

Neal, C. (1988). Aluminium solubility relationships in acid waters - a practical example of the need for a radical reappraisal. Journal of Hydrology, 104, 141-159. 

Automatic water samplers at each of these sites were triggered when the water level reached a pre-set height. Composite samples, made up of four half-hourly sub-samples, were taken at two hour intervals for 48 hours. These samples, which were taken to monitor changes in water chemistry during episodes of high flow, were analysed for pH, alkalinity, calcium, magnesium, aluminium (soluble and total after acidification of the sample), conductivity, chloride and humic substances. 

C22H23N3O9. An organic reagent used for the detection and estimation of aluminium. It is a brownish-red powder, soluble in water which gives a red lake with aluminium which can be estimated colorimetrically. It can also be used for detecting scandium and indium. 

The aluminium ion, charge -I- 3. ionic radius 0.045 nm, found in aluminium trifluoride, undergoes a similar reaction when a soluble aluminium salt is placed in water at room temperature. Initially the aluminium ion is surrounded by six water molecules and the complex ion has the predicted octahedral symmetry (see Table 2.5 ) ... 

The electrode potential of aluminium would lead us to expect attack by water. The inertness to water is due to the formation of an unreactive layer of oxide on the metal surface. In the presence of mercury, aluminium readily forms an amalgam (destroying the original surface) which is. therefore, rapidly attacked by water. Since mercury can be readily displaced from its soluble salts by aluminium, contact with such salts must be avoided if rapid corrosion and weakening of aluminium structures is to be prevented. 

Why is potassium aluminium sulphate not soluble in benzene A compound M has the composition C = 50.0% H=12.5%o A1 = 37.5%. 0.360 g of M reacts with an excess of water to evolve 0.336 1 of gas N and leave a white gelatinous precipitate R. R dissolves in aqueous sodium hydroxide and in hydrochloric acid. 20 cm of N require 40 cm of oxygen for complete combustion, carbon dioxide and water being the only products. Identify compounds N and R, suggest a structural formula for M, and write an equation for the reaction of M with water. (All gas volumes were measured at s.t.p.)... 

Aqueous ammonia can also behave as a weak base giving hydroxide ions in solution. However, addition of aqueous ammonia to a solution of a cation which normally forms an insoluble hydroxide may not always precipitate the latter, because (a) the ammonia may form a complex ammine with the cation and (b) because the concentration of hydroxide ions available in aqueous ammonia may be insufficient to exceed the solubility product of the cation hydroxide. Effects (a) and (b) may operate simultaneously. The hydroxyl ion concentration of aqueous ammonia can be further reduced by the addition of ammonium chloride hence this mixture can be used to precipitate the hydroxides of, for example, aluminium and chrom-ium(III) but not nickel(II) or cobalt(II). 

By treatment with anhydrous aluminium chloride (Holmes and Beeman, 1934). Ordinary commercial, water-white benzene contains about 0 05 per cent, of thiophene. It is first dried with anhydrous calcium chloride. One litre of the dry crude benzene is shaken vigorously (preferably in a mechanical shaking machine) with 12 g. of anhydrous aluminium chloride for half an hour the temperature should preferably be 25-35°. The benzene is then decanted from the red liquid formed, washed with 10 per cent, sodium hydroxide solution (to remove soluble sulphur compounds), then with water, and finally dried over anhydrous calcium chloride. It is then distilled and the fraction, b.p. 79-5-80-5°, is collected. The latter is again vigorously shaken with 24 g. of anhydrous aluminium chloride for 30 minutes, decanted from the red liquid, washed with 10 per cent, sodium hydroxide solution, water, dried, and distilled. The resulting benzene is free from thiophene. 

The higjily water-soluble dienophiles 2.4f and2.4g have been synthesised as outlined in Scheme 2.5. Both compounds were prepared from p-(bromomethyl)benzaldehyde (2.8) which was synthesised by reducing p-(bromomethyl)benzonitrile (2.7) with diisobutyl aluminium hydride following a literature procedure2.4f was obtained in two steps by conversion of 2.8 to the corresponding sodium sulfonate (2.9), followed by an aldol reaction with 2-acetylpyridine. In the preparation of 2.4g the sequence of steps had to be reversed Here, the aldol condensation of 2.8 with 2-acetylpyridine was followed by nucleophilic substitution of the bromide of 2.10 by trimethylamine. Attempts to prepare 2.4f from 2.10 by treatment with sodium sulfite failed, due to decomposition of 2.10 under the conditions required for the substitution by sulfite anion. 

When the phase diagram for an alloy has the shape shown in Fig. 10.3 (a solid solubility that decreases markedly as the temperature falls), then the potential for age (or precipitation) hardening exists. The classic example is the Duralumins, or 2000 series aluminium alloys, which contain about 4% copper. 

The alloy aluminium-4 wt% copper forms the basis of the 2000 series (Duralumin, or Dural for short). It melts at about 650°C. At 500°C, solid A1 dissolves as much as 4 wt% of Cu completely. At 20°C its equilibrium solubility is only 0.1 wt% Cu. If the material is slowly cooled from 500°C to 20°C, 4 wt% - 0.1 wt% = 3.9 wt% copper separates out from the aluminium as large lumps of a new phase not pure copper, but of the compound CuAlj. If, instead, the material is quenched (cooled very rapidly, often by dropping it into cold water) from 500°C to 20°C, there is not time for the dissolved copper atoms to move together, by diffusion, to form CuAlj, and the alloy remains a solid solution. 

The chemical behavior of Franklin acidic chloroaluminate(III) ionic liquids (where X(A1C13) > 0.50) [6] is that of a powerful Lewis acid. As might be expected, it catalyzes reactions that are conventionally catalyzed by aluminium(III) chloride, without suffering the disadvantage of the low solubility of aluminium(III) chloride in many solvents. 

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