More sugar, more reducing ends to get oxidized to -COOH?
I see. Thanks, AJ. I've been spending the last hour sort of following chains, much like you recommend: "when you come across something you don't understand, go off on a side investigation...." and it of course leads to a pretty wide sea-sojourn. So this is another one, this notion. Fascinating.
Thanks. I wonder if I could ask for what may be a bit of a subjective response? Needing acid, I know the virtues now of lactic, and phosphoric. I've got this bottle of 37% HCL that I'll dilute to 10% (or 1N, possibly?), wanting to play with British practice. If I could find food-grade sulfuric, I'd join them in a kind of made-up CRS. Is there any reason to believe not all sulfates or chlorides are the same? Salt or acid, we're doing the same thing (while strongly releasing H+ into solution with the acids)?
I think you may be referring to DeClerk's recommendations for calculating lime additions. He gives a procedure for doing this and then recommends treating three samples with the calculated amount and also ±10% of the calculated amount. You then use the dose that gave the best decarbonation scaled to the full volume to be treated.
Thanks, found it. Seeing your discussion with Silver on the potential low quality of store-bought RO (our local coop has a machine, but I've extremely little confidence now that they maintain it properly. Duuuude. Wanna mango? ya know....). And I've never lost the desire to at least try a more traditional approach to water treatment, whether it be boiling or lime. I've got the 10 pages up begun by Yooper, and am looking forward to trying it out. With Mg reported as 41 ppm, I do think I'll do a split regime, and learn what to do after, to measure what needs to be put back in. Thanks.
Basically, I think, the plan is to drop carbonate out, put needed ions back in, and adjust to mash pH of 5.2-5.4 with acid; storing all in a liquor tank, of sorts, for brew day. Is that reasonable?