Post
by Carnot » Thu Dec 24, 2020 10:08 pm
I will try and keep this simple. To all intents, calcium carbonate is barely soluble in water. Very roughly 20 mg/L will dissolve in water as the carbonate. In the presence of carbon dioxide more calcium carbonate will dissolve as calcium bicarbonate is formed, which is soluble in the hundreds of mg/L, subject to certain conditions. See the reationship in the previous post by Peebee. I spent my early years as a water treatment chemist. The reason why we use measurements as CaCO3 was for ease of calculation. In my early days we only had simple caculators and ready reckoners so the muliples had to be easy. I performed many tests of alkalinity and hardness determinations every day and we had to do these quickly and accuratley. Since calcium carbonate had a molecular weight of 100 reporting as CaCO3 was like using a common currency, so all measurment were done as CaCO3 (there we exceptions like iron, chromate, copper, etc).
Your question fo why does chalk dissoolve in the mash is a little more complicated and it puzzled me for some time. Why does the addition of calcium lower the mash pH. All was revealed on page 66 of Water. A comprehensive guide for brewers- ISBN 978-0-937381-99-1. The best £14 you can spend on brewing. In short malted barley contains about 1% (10,000 mg/L) phosphate as phytic acid salts( K and Mg). These phytin salts react with calcium, via many pathways, and the net result is that calcium reacts with the phosphate and releases hydrogen ions which depress the pH(increase the hydrogen ion concentration) and also releases carbon dioxide. The calcium carbonate dissolves but the calcium is precipitated as calcium phospate (solubility about 1-2 mg/L) and carbon dioxide is liberated. The net effect is that the mash pH is lowerd BUT the calcium concentration is barely affected. These reactions can only occur in the mash tun and not in the HLT as it is the phytic acid that allows the dissolution of the calcium carbonate and the precipitation of the calcium as the phosphate. I hope that you can follow this but if not then please tell me where I lost you.
I will not labour the point too much, but many, especially Eric, place much emphasis on alkalinity rather than pH. Measuring pH at mash conditions is especially difficult. You need to get your head around pH, which is a measure of the negative log of the hydrogen ion concentration. pH 5 is a measure of 10 power negative 5, which is effectively micro g/L or 10 ppb in old money. in simple words sod all, and that makes accurate determnation a little tricky, especially when dealing with sugary solutions, and also remember that pH is temperature dependent.