Norselord
Well-Known Member
I am getting ready to rack an IPA onto hops in a secondary.
I was thinking that i would do a quick and dirty cold-crash the primary to get it to clear out a bit, then rack onto hops in secondary. I was going to let the secondary warm back up in a fermentation chamber set to 67F. Then after 4 days cold crash with gelatin and rack to keg.
I have heard so many opinions on why this is wrong or right. Anyone want to share their way of doing it and then justify their process with something close to science? I.E. not: that's how i have always done it, or that's how Brewer McAwesome does it, etc.
My reason for the process i described above is as follows:
1) i want to remove suspended solids from the primary so that the hop oil can more completely and efficiently be absorbed into the beer.
2) i want the secondary to get a little warmer since most substances dissolve into liquid more readily at warmer temperatures.
3) I am not scared of crashing the secondary with gelatin because it will only pull protein and other suspended solids out - the hope oils are dissolved and will stay in solution.
Thoughts?
I was thinking that i would do a quick and dirty cold-crash the primary to get it to clear out a bit, then rack onto hops in secondary. I was going to let the secondary warm back up in a fermentation chamber set to 67F. Then after 4 days cold crash with gelatin and rack to keg.
I have heard so many opinions on why this is wrong or right. Anyone want to share their way of doing it and then justify their process with something close to science? I.E. not: that's how i have always done it, or that's how Brewer McAwesome does it, etc.
My reason for the process i described above is as follows:
1) i want to remove suspended solids from the primary so that the hop oil can more completely and efficiently be absorbed into the beer.
2) i want the secondary to get a little warmer since most substances dissolve into liquid more readily at warmer temperatures.
3) I am not scared of crashing the secondary with gelatin because it will only pull protein and other suspended solids out - the hope oils are dissolved and will stay in solution.
Thoughts?