nyer
Well-Known Member
One more quick question, if I'm making a 5 gallon batch but using 10 gallons of water total I am making the additions based on the 10 gallons of water total? It's not batch size but total water used right?
Yes, that's correct. As low alkalinity water is being used as the starting point there is no need to acidify the sparge water or treat it any differently than the mash water. Some brewers do that, add salts to the kettle etc. but none of those techniques fall under the KISS principle which underlies the Primer.
This is flame bait. It doesn't work theoretically (i.e. a phosphate buffer at mash pH is a weak one because mash pH is distant from either of the closest 2 pK's of the phosphate system) and it doesn't work in lab tests. Plus in DI water it buffers to 5.8 or so. It relies on the phosphate from the malt to form a lower pH buffer but treble the suggested dose in real malt grists using water of modest (80) alkalinity it only gets you to 5.4 or so.
Do not trust him. Do your own experiment. If you are take pH measurements on 5.2 solutions and read 5.2 then your meter is broken or your buffers are off - way off.
Actually, I disproved it analytically and demonstrated the fallacy in the lab.THANK YOU!!! For proving my point exactly!!!
You add a few teaspoons of 5.2 powder to your water and add some BARLEY (I mean who would have thought of adding malted barley to a homebrew recipe?) and you get a pH of 5.2!
Without reading 31 pages of mumbo jumbo or spending hours worrying about your water.
That I would like to see.I tested it last night - I'd be happy to youtube it.
Apparently you aren't or you would at least respond to the buffer strength argument.I spent over a decade as a Nuclear Chemist doing pH analysis dozens of times a day so I am very very familiar with how it works, how the calibration buffers work and what a simple buffer such as 5.2 is actually doing.
It works and you don't need a PhD to get it to work - just a measuring spoon and 2 minutes of time!
PS - I also don't rotate my truck's tires every 5000.000 miles like the salesman told me to but I still get 68,000 miles out of the 70,000 they advertised.... Saves me hundreds of hours of not waiting in his showroom!
There's one in every crowd.
Thanks for all of the helpful information you have provided in this thread and others I have followed AJ.
Let me give you my wife's e-mail address....You are a very patient man AJ.
The debate on 5.2 in general - in my opinion if it takes tap water in the 7 to 8 range and drops it to the 5 range that is a success. I realize it does NOT get it down to an actual 5.2 but relies on the grain to finish the job. Are others even able to get it to do this initial drop in pH? It appears to be a fairly quick and easy method to drop standard carbon filtered tap water (note - my tap water is very soft - 30 ppm range soft).
Thanks All!
Perhaps another way to gain some perspective on this is to consider a water alkaline enough that a base malt mash comes in at pH 5.8. Since it is claimed that 5.2 will bring the pH of this mash to 5.2 we note that a drop of 0.6 pH is required of the product.
You are the first person that I have seen claim that it works based on a pH meter reading. Plenty of other guys have tried it and any who have used a pH meter to check on what it is doing have come to the same conclusion I have.
Can you tell us more about what you mean when you say it works. Clearly this would imply that you get mash pH of 5.2 but at what temperature? At what phase in the mash? With what sort of grist? Etc.I'm still working on some data, but I still find that 5.2 works for me with my water and my grist.
This is pretty easy water. I don't see any problems with it.Calcium 57 MG/L
Magnesium 16 MG/L
Sodium 14 MG/L
Chloride 3 MG/L
Sulfate 5.0 MG/L
Alkalinity 10MG/L
PH is 7.21
I have begun to suspect that the biggest problem with the inexpensive meters may be that they drift and/or have a stability criterion that is too relaxed such that they grab calibration measurements before they should (i.e. before allowing the potential to really come to equilibrium). ATC should always be regarded with suspicion. If the electrode's isoelectric pH is off ATC can induce quite a bit of error. For this reason buffers and samples should all be at the same, or nearly the same, temperature.And, this is the pH meter I'm using; do you see any flaw with it? I know temperature plays a role, and this purports to be ATC; though I honestly have my doubts about anything that claims ATC.
Can you tell us more about what you mean when you say it works. Clearly this would imply that you get mash pH of 5.2 but at what temperature? At what phase in the mash? With what sort of grist? Etc.
I have begun to suspect that the biggest problem with the inexpensive meters may be that they drift and/or have a stability criterion that is too relaxed such that they grab calibration measurements before they should (i.e. before allowing the potential to really come to equilibrium). ATC should always be regarded with suspicion. If the electrode's isoelectric pH is off ATC can induce quite a bit of error. For this reason buffers and samples should all be at the same, or nearly the same, temperature.
Step 11b in the pH Calibration Sticky is designed to detect problems with stability and isoelectric pH. Be sure you do that check.