So, how does this tie into the big tease of a post title? I am going to be brewing a big barleywine that will essentially max out my mash tun capacity twice. My particular setup is very well suited to performing this kind of iterated mash. Instead of using a false bottom or bazooka screen, I simply line my cooler with a BIAB bag. This will let me pull out my grains after the initial mash, then add a fresh batch of grain back to the mash water for a second mash using the wort from the first mash as my liquor.
The goal here is two-fold. The primary goal is to achieve a pre-boil gravity that is well beyond what I could possibly produce on my system from a single mash. The second goal is to maximize fermentability by being able to perform a true reverse-step mash. So what the heck does that mean?
First, here's a quick refresher on enzymes in the mash. I'll try to keep this at "for Dummies" level. Most all-grain brewers are at least a little familiar with alpha and beta amylase. Beta amylase is most active at lower mash temperatures (140-150F), and tends to produce more simple sugars, which in turn leads to increased fermentability. Alpha amylase is most active at higher mash temperatures (162-167F), and tends to produce more dextrins, which leads to a less fermentable wort.
But here's where it gets interesting. The action of alpha amylase produces more food for beta amylase to do its thing. Even more interesting is an enzyme that we don't really target in a typical mash: limit dextrinase. Limit dextrinase is able to break down the dextrins that are left over after alpha and beta amylase have done their thing. The problem is that it is active at temperatures lower than even beta amylase (133-140F), and it is gone before alpha amylase even gets started.
In a typical mash, once you raise the temp above the point where an enzyme gets denatured, you essentially lose that enzyme from that point on. In a single mash, once you raise the mash temp to alpha-amylase's optimum range, you start to lose beta-amylase activity, and limit-dextrinase is already long gone. You can't begin a traditional mash with a high-temp alpha rest, then drop the temp to beta rest range, then drop it again to limit dextrinase range. The enzymes have already been denatured at the initial high mash temp.
If only there was a way to bring back beta amylase and limit dextrinase after your high mash rest. But wait - there is! Just add more malt. And we finally get back to what I'm trying to do here. Basically, I'm going to do a high temperature mash with 8 pounds of grain in my mash tun. Then I'm going to pull my grain out, and add another 8 pounds back in. This second mash will be held at a low enough temperature where both beta amylase and limit dextrinase will be active. Hopefully, I'll end up with a super-fermentable wort that will enable me to brew a giant beer that can still ferment down to a reasonable FG.
So without further ado - here's the recipe. I have no clue what my efficiency is going to be, so this is calculated on 60%. But I typically hit 80% or so, even on beers this big. If so, this is going to be a really big beer.
Title: Giant Freaking Barley Wine
Brew Method: BIAB
Style Name: English Barleywine
Boil Time: 90 min
Batch Size: 3 gallons (fermentor volume)
Boil Size: 3.7 gallons
Boil Gravity: 1.099
Efficiency: 60% (brew house)
STATS:
Original Gravity: 1.122
Final Gravity: 1.024
ABV (standard): 12.77%
IBU (tinseth): 68.83
SRM (morey): 11.65
FERMENTABLES:
8 lb - United Kingdom - Maris Otter Pale (50%)
8 lb - United Kingdom - Maris Otter Pale (50%)
HOPS:
1 oz - Magnum, Type: Pellet, AA: 15.4, Use: Boil for 60 min, IBU: 63.04
1 oz - East Kent Goldings, Type: Pellet, AA: 7.1, Use: Boil for 5 min, IBU: 5.79
MASH GUIDELINES:
1) Infusion, Temp: 160 F, Time: 45 min, Amount: 16 qt, Mash #1
2) Infusion, Temp: 145 F, Time: 90 min, Amount: 14 qt, Mash #2
YEAST:
White Labs - Yorkshire Square Ale Yeast WLP037
TARGET WATER PROFILE:
Profile Name:
Ca2: 85
Mg2: 25
Na: 11
Cl: 78
SO4: 150
HCO3: 0
Water Notes:
2 g Gypsum
4 g Epsom Salt
2.5 g CaCl2
2 mL Lactic Acid
(All added to initial mash water)
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