You may find it helpful to revise about acids, bases and salts. Aluminium sulphate is
a salt. It could be produced by the reaction you quote, but with the arrow reversed.
Asking what has happened to the sulphuric acid is like asking the same question about sodium sulphate. You can think of it as having been neutralised by the base Al(OH)
3.
To a first approximation salts are neutral. However to a better approximation, It is not quite like sodium sulphate because that is the salt of a strong acid and strong base, whilst aluminium sulphate is salt of a strong acid and weak base. The salt of a strong acid and weak base will be slightly acid. This is because - just take the example of ammonium sulphate - the conjugate base SO
42- of the strong acid has little tendency to be protonated, while the conjugate NH
4+ of the weak base NH
3 has some tendency to 'lose' the proton (i.e. transfer it to water). So there is a greater concentration of protons than in pure water. Maybe it hasn't been very apparent but there is an exact analogy:
[Al.(H
2O)
6]
3+ plays a role like NH
4+, and [Al.(H
2O)
5OH]
2+ like NH
3
I would still like to know where this K
b you quote comes from. If this is the K
b for the equilibrium between the last mentioned forms, it fits reasonably with the pK
a I found here
http://chemwiki.ucdavis.edu/Core/In...iod_3_Elements/Chlorides_of_Period_3_Elements of 3.3 to 3.6. But Al(OH)
3 is something different.
As to how you calculate the pH, this is pretty much as you have done it. However I should do it again. It seems to me that the total molarity [Al] is twice your figure, taking into account the two atoms/molecule in the starting formula.
Also I should say that [Al.(H
2O)
6]
3+ is not all that weak an acid. It's more in the category 'moderately weak' or 'moderately strong' - base. likewise its conjugate a moderately weak - or moderately strong base. In fact I get pH around 3.5, getting to be a moderately acid solution, and the last-mentioned species about half deprotonated.