Quote:
Originally Posted by thebigt85
Regarding mash pH, I agree that I'd need to lower it, as the alkalinity of my water isn't enough to overcome the buffering capacity of the mash and bring the pH down to acceptable levels (is this correct?)
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Other way round. Base malts buffer to pH higher than you want and the buffer in the water (carbonic/bicarbonate) is higher than you want (7.2) in your case so you need an acid/base pair with pK lower than malt or water to overcome the buffering of the grains and the water.
Quote:
Originally Posted by thebigt85
I have access to both HCl and sulfuric acid, but I haven't done any buffer system calcs in a while and would be a bit rusty. Is there a resource online for help with this?
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Here it is very straight forward. Each grain has a DI mash pH. If you model the titration curve as a Taylor series expanded about the mash DI pH and if, in particular, you assume that only 2 terms in the expansion are necessary you can figure out how much acid would be needed for particular mash pH for each of the grains:
acid_requirement = (target_pH - DI_pH)*buffering_capacity*wt_grain.
For example, if you want pH 5.4 and are mashing 5 kg Maris Otter which has a DI pH of about 5.6 the acid required would be
acid_requirement = (5.4 - 5.6)[pH]*(-21)[mEq/kg-pH]*5[kg]= 21 mEq
for the Maris Otter alone. If you have 1 kg of a grain with a DI pH of 5.1 the requirement is
(5.1 - 5.4)*-21*1 = -6.3 mEq
You do this for each malt and sum up the results. If the sum is positive you add that much acid. If negative you add that much base.
Weyermann maltings has a rule of thumb that says 1% (w/w) sauermalz in the grist lowers the pH 0.1 unit. The -21 mEq/kg-pH number is derived from that rule of thumb assuming that sauermalz is 2% lactic acid w/w. Using that rule of thumb is certainly easier than the calculations.
There are also lots of spreadsheets and calculators which will do this for you though I am not sure about what the algorithms are for any of them. Or to be more honest about it, I haven't a clue. Some of them try to back things out from malt color, for example.
Obviously to do the job right you need to know the DI mash pH and all the pertinent Taylor series terms for each malt. I have no assurance that 2 terms are enough but I am certain that there is appreciable deviation from the -21 mEq/kg-pH value with some malts.
Rather than deal with the uncertainties I recommend making a test mash and measuring the pH of that. You can certainly use any of the spreadsheets or calculators to get you in the ball park but IMO the final determination should be based on measurement.