Hey all,
Me and my buddy have completed 3 extract brews (3rd one is bottle conditioning now - have had a taster so far) and we've used these forums as a great resource for our questions along the way. I know its all trial and error, but I've noticed a consistent "off" flavor in our last 2 kits that wasn't there in our first. After trying to retrace my steps and figure out what we did differently to cause this, and what this "off" flavor might be, I think I've found it may be down to 2 things:
1) The "extract" off flavor that some describe by letting the DME caramelize during the boil could definitely be it - I've read about doing the late add at flameout and also about taking the kettle off the heat when adding the initial extract and will test these methods during out next brew.
2) Potential oxidation gained either through oxidizing hot wort, or during racking procedures, or perhaps overzealous checking of the primary fermenter.
I would best describe the off flavor as being "yeasty" and the brews are definitely a bit cloudy. However, my palate may not be sophisticated enough to truly pinpoint it. Anyway, related to some "common mistakes" I've been reading up on that we could be making, wanted to propose 2 questions to the "experts" here and see what we might be messing up. Thanks in advance.
1. Preventing oxidation of the wort: We don't have a wort chiller so during our first 2 batches when temperatures were warmer, we used a tub filled with ice to try and cool our wort. I believe we kept the brew kettle's lid off during this - looking back, is this a big no-no? And during the most recent batch, since we were in the dead of winter and had some convenient snow piles in my yard, we put the kettle right into one of those (again, the lid may have been off). Additionally, we stir the cooling wort around to try to get the warmer wort at the bottom of the kettle to react to the cold air. This could all be a big mistake - without a wort chiller for now, would a better method of cooling just be to cover the wort and put it in an extra fridge? I'm lucky to have basement fridge that I could take the racks out of and easily fit the brew kettle in there?
Additionally, to aerate our wort, my partner has a pump he otherwise uses in fishing (not a fisherman myself so I don't necessarily understand it) that we keep on the additional 2.5-3g of water that will be added to the chilled wort and we splash our wort on top of that (straight from brew kettle to fermenter). Is that not sufficient aeration? On the opposite end, is the "splashing" of the cooled wort potentially oxidizing it?
2. Racking procedures: I know I've read enough know to believe that a secondary is probably not necessary. I think what we're going to do this time is strain our wort into the primary and try to just leave it in the primary for 3-4 weeks before going right to the bottling bucket. Questions on this:
- Is the plastic "kit" primary bucket preferable to a plastic carboy for a primary fermentation? If I'm only using one of the other (eliminating the secondary process), which should I use, and why?
- What are the best ways to prevent any oxidation potential if we did decide to rack to a secondary? We've used a racking cane and siphon to date for this and may have made errors. First, obviously we remove the air-tight lid on the primary to take our FG readings and start the racking process and leave it off throughout - should the lid be replaced while the siphon is going? If so, how can you siphon through the standard grommets (our racking cane is quite a bit thicker than the grommet). Then, to get the siphon started, I've been just doing the "sucking" technique, which is probably an issue - whats a better way to start the siphon if you DON'T have an auto-siphon? Then, while I'm careful as the carboy fills to ensure the siphon is below the beer line, obviously initially there is no beer line and splashing seems inevitable (as well as an open top in the carboy) - I'm thinking this may be where I'm getting the worst oxidation potential. How is this avoided? Finally, if there is extra room in the carboy, should this be somehow filled? My latest batch turned out to only be about 4 gallons presumably due to some boil off and a lot of trub in the primary left behind - did this extra space in my carboy cause some problems? Finally, during the racking process to the bottling bucket, I think my kit instructions tell me to stir the priming sugar (after its boil) into the transferred flat beer, but does this stirring in the un-topped bottling bucket again cause some oxidation? Whats the preferred method HERE?
Thanks again everyone. I know this is a LONG post, but I really appreciate any feedback that can be provided. I think the good news is that the "off" flavor I've tasted is definitely consistent so I assume its something easily correctable in our brew process and hoping to just pinpoint where its originating from.
Me and my buddy have completed 3 extract brews (3rd one is bottle conditioning now - have had a taster so far) and we've used these forums as a great resource for our questions along the way. I know its all trial and error, but I've noticed a consistent "off" flavor in our last 2 kits that wasn't there in our first. After trying to retrace my steps and figure out what we did differently to cause this, and what this "off" flavor might be, I think I've found it may be down to 2 things:
1) The "extract" off flavor that some describe by letting the DME caramelize during the boil could definitely be it - I've read about doing the late add at flameout and also about taking the kettle off the heat when adding the initial extract and will test these methods during out next brew.
2) Potential oxidation gained either through oxidizing hot wort, or during racking procedures, or perhaps overzealous checking of the primary fermenter.
I would best describe the off flavor as being "yeasty" and the brews are definitely a bit cloudy. However, my palate may not be sophisticated enough to truly pinpoint it. Anyway, related to some "common mistakes" I've been reading up on that we could be making, wanted to propose 2 questions to the "experts" here and see what we might be messing up. Thanks in advance.
1. Preventing oxidation of the wort: We don't have a wort chiller so during our first 2 batches when temperatures were warmer, we used a tub filled with ice to try and cool our wort. I believe we kept the brew kettle's lid off during this - looking back, is this a big no-no? And during the most recent batch, since we were in the dead of winter and had some convenient snow piles in my yard, we put the kettle right into one of those (again, the lid may have been off). Additionally, we stir the cooling wort around to try to get the warmer wort at the bottom of the kettle to react to the cold air. This could all be a big mistake - without a wort chiller for now, would a better method of cooling just be to cover the wort and put it in an extra fridge? I'm lucky to have basement fridge that I could take the racks out of and easily fit the brew kettle in there?
Additionally, to aerate our wort, my partner has a pump he otherwise uses in fishing (not a fisherman myself so I don't necessarily understand it) that we keep on the additional 2.5-3g of water that will be added to the chilled wort and we splash our wort on top of that (straight from brew kettle to fermenter). Is that not sufficient aeration? On the opposite end, is the "splashing" of the cooled wort potentially oxidizing it?
2. Racking procedures: I know I've read enough know to believe that a secondary is probably not necessary. I think what we're going to do this time is strain our wort into the primary and try to just leave it in the primary for 3-4 weeks before going right to the bottling bucket. Questions on this:
- Is the plastic "kit" primary bucket preferable to a plastic carboy for a primary fermentation? If I'm only using one of the other (eliminating the secondary process), which should I use, and why?
- What are the best ways to prevent any oxidation potential if we did decide to rack to a secondary? We've used a racking cane and siphon to date for this and may have made errors. First, obviously we remove the air-tight lid on the primary to take our FG readings and start the racking process and leave it off throughout - should the lid be replaced while the siphon is going? If so, how can you siphon through the standard grommets (our racking cane is quite a bit thicker than the grommet). Then, to get the siphon started, I've been just doing the "sucking" technique, which is probably an issue - whats a better way to start the siphon if you DON'T have an auto-siphon? Then, while I'm careful as the carboy fills to ensure the siphon is below the beer line, obviously initially there is no beer line and splashing seems inevitable (as well as an open top in the carboy) - I'm thinking this may be where I'm getting the worst oxidation potential. How is this avoided? Finally, if there is extra room in the carboy, should this be somehow filled? My latest batch turned out to only be about 4 gallons presumably due to some boil off and a lot of trub in the primary left behind - did this extra space in my carboy cause some problems? Finally, during the racking process to the bottling bucket, I think my kit instructions tell me to stir the priming sugar (after its boil) into the transferred flat beer, but does this stirring in the un-topped bottling bucket again cause some oxidation? Whats the preferred method HERE?
Thanks again everyone. I know this is a LONG post, but I really appreciate any feedback that can be provided. I think the good news is that the "off" flavor I've tasted is definitely consistent so I assume its something easily correctable in our brew process and hoping to just pinpoint where its originating from.