Homebrew Digest Wednesday, 10 July 1996 Number 2099

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   FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
        Shawn Steele, Digest Janitor
        Thanks to Rob Gardner for making the digest happen!

Contents:
  distilled water? (brewshop at coffey.com (Jeff Sturman))
  Qouth AlK / Plastic Carboys / BS in the BA / Virgin's Stout (KennyEddy at aol.com)
  Re: Boil-over cleanup. (stafford at newport26.hac.com (Jack Stafford))
  Re: 158F mashing ("Tracy Aquilla")
  Re: White film in bottled beer...yuck or yum?! (WineNBrew at aol.com)
  A  WWW page! (Mark Wallace/CAM/Lotus)
  re: Mashing Time - another point of view. (Steve Alexander)
  thermal contraction problem? ("Ray Robert")
  Fermentability (John Chang)
  Re: hi temp mash-source of sweetness? ("Tracy Aquilla")
  Re: Al & Dave's little tiff ("Tracy Aquilla")
  OOPS! A quick add-on re: cleaning (WineNBrew at aol.com)
  Mash temperature experiment (stafford at newport26.hac.com (Jack Stafford))
  Bug killers didest #2098 (blades at airtime.co.uk (Liz Blades))
  RE: HYPERBOLE (Carl Hattenburg)
  Yeast and ITBR? ("Craig Rode")
  Beer in Spaaace ("Goodale, Daniel CPT 4ID DISCOM")
  Skunked Beer (Jeff Hewit)
  Burley vs. Korzonas (korz at pubs.ih.lucent.com)

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---------------------------------------------------------------------- From: brewshop at coffey.com (Jeff Sturman) Date: Tue, 9 Jul 1996 11:49:59 -0600 Subject: distilled water? Last weekend I had some minor pH problems with my mash and out of curiosity I checked the pH of the distilled water I use. My tap water sucks, so I mix it about 50/50 with distilled water when I brew. Two different brands of pH papers and a digital pH meter all calculated the pH of the distilled water at about 5.5! Isn't distilled water supposed to be pH 7.0? The manufacturer of the water told me that distilled water, pH 7.0, is corrosive because it acts like a sponge, trying to suck up anything it contacts. That's why their distilled water has a lower pH. Are they pulling my racking cane? jeff Return to table of contents
From: KennyEddy at aol.com Date: Tue, 9 Jul 1996 14:03:27 -0400 Subject: Qouth AlK / Plastic Carboys / BS in the BA / Virgin's Stout AlK Suggests: << Before, I go on, I'd like to ask that we all try to not use all 80 columns in our posts. It makes it that much harder to quote and insert the ">" at the beginning without wrapping. I try to never use the 80th column in any post for fear that the HBD engine will reject the post. >> Maybe a different "quoting" technique, such as the one illustrated here, is a better approach than trying to get your CR's in the right spot when writing and rewriting a post. I'll test drive it here -- ********** Duff Hickman asked: << Has anyone tried using the plastic water bottle jugs (the ones used in office dispensers) for fermentation? They are the same shape and have a >> When I started brewing, I used one of these (in fact, I still have it). My earlier brews were pretty uninspiring, for a number of reasons, but I don't think using the plastic as a primary fermenter was the main culprit. Problem is, I changed a buch of things in my brewing process to improve my product (which it did); I can't say what the difference was with respect to the plastic bottle. I'll go out on a limb and say that the limited time that a beer is in primary (maybe a week) should present a minimal oxidation hazard; in fact, while the yeast are active, they can consume some of what does get in (significant amount? I dunno). If you stick to simple so-called "quick ales" (a week in primary then right into bottles) or use a glass secondary, I wouldn't sweat it. By the way, you'll also need a larger stopper than the glass carboys; I think it's a #9 or #9-1/2 but I may be wrong. ********** Jim Thomas' brown ale has him puzzled: << Sort of watery, but I wouldn't call it thin. Don't know if this is how this mild brown is supposed to taste. I'm wondering if the brown sugar is the culprit. Don't think it's the yeast, although I've not used this strain before. >> I haven't used brown sugar very often but a friend of mine does, and it tends to be pretty coarse until it ages a while. Not sure "watery" comes to mind, but it definitely needs aging if there's a significant amount of BS in there. *********** Mike Kidulich is going for a Classic on his virgin AG session: << Guinness Alike 8 lb. British Pale malt 1 lb. roasted barley 1 lb. flaked barley bittering hops (haven't decided what to use yet) Wyeast Irish (1084) from starter >> My wife just brewed and bottled almost this same recipe (7 lb pale malt; 1-1/2 lb FB I believe) and this simple recipe (a' la Lewis' "Irish Draught Stout") was QUITE reminiscent of draught Guiness when we popped one open on her birthday (after the requisite fourteen-day waiting period). Brewing Details: Delia used a 154F single-temperature mash for a bit over an hour. For bittering she used Kent Golding plugs to the tune of 40 - 45 IBU's (2 oz at ~5% I think, for 60 minutes after a 30-min wort pre-boil). Wyeast Irish was also used. Fermented at 68F. One week primary, one week secondary. Primed with 1/2 cup corn sugar and bottled -- the carbonation is just about right at that level. The water was fairly soft, RO with enough baking soda (2g per 5 gal) and chalk (0.25g) to boost the alkalinity to about 75 ppm, and deriving most of the calcium for mashing from CaCl2 (3.5g). She used a pinch of epsom salt (0.5g) to bring the sulphate to about 10 ppm. Mash pH was 5.2 with this formulation. If you use your regular brewing water, have some chalk handy to adjust the pH since the roasted barley may drive the pH below 5.0, depending on your water makeup. It's a surprise to many to learn that draft Guiness is a relatively light-gravity beer (something like 1.038 OG); its robust flavor and aroma can give the impression of a much stronger brew. Delia stepped up the Lewis recipe from 1.038 to about 1.045; I think it's perfect at that level (but then again I like math too). The above recipe will result in an OG somewhere at or above 1.050 -- give it some thought. Best luck o' the Irish to ye, son. *********** Ken Schwartz KennyEddy at aol.com http://users.aol.com/kennyeddy Return to table of contents
From: stafford at newport26.hac.com (Jack Stafford) Date: Tue, 9 Jul 96 11:16:52 PDT Subject: Re: Boil-over cleanup. Sun, 7 Jul 1996, Mike Foster <mfoster1 at voyager.net> wrote: >My second batch boiled over two days ago, and now I have carbonized wort >stuck to my wife's enameled white stove. How can I get this stuff off >without ruining the finish of the stove? Oven cleaner should do the trick. Hang in there, it looks gnarley but don't let a little boilover scare you off. :) Jack Costa Mesa, CA Return to table of contents
From: "Tracy Aquilla" <aquilla at salus.med.uvm.edu> Date: Tue, 9 Jul 96 14:25:12 CDT Subject: Re: 158F mashing In Digest #2097: <korz at pubs.ih.lucent.com> Al K. wrote: >Dave writes: >>The nerve of that AlK telling me to admit that I'm wrong and in public!. Well >>I never...... > >I felt it important to point out that you have >been posting misinformation numerous times on this topic. Please be specific here, Al. Exactly which information was incorrect? >>Does George DePiro's comment, a couple of HBD's ago, that one would get a >>"barely fementable wort" by saccharifying at 158 F, mean anything to you? > >It means that (Gold Medal Winner) George has the concept right, but perhaps >exaggerated a bit regarding the unfermentability of the resultant wort. More than a bit, IMO. "Barely fermentable" misses the mark entirely. David has made a valid observation here. >>I gave an example of a >>recent brew of mine which clearly showed that George's comments were off base. >>My brew had a reasonable FG ( 1.015 - which is what I wanted) and good >>fermentability ( OG of 1.060 - 1.015) and a calculated efficiency of >>extraction of 89%. Frankly, I am surprized at the continued reaction I get >>to what I thought was an innocent comment during a diatribe on a different >>subject. > >Your 75% apparent attenuation could be explained in a variety of ways. Your >[snip]...There are a lot of other possibilities, but it's time to move on. Hold on there, I'm not ready to move on just yet. I have mashed many beers at 157, 158, and even 159F using a single infusion. This is how I usually make scotch ales. I use multiple, carefully calibrated thermometers, have no infections, and do single infusions of hot water. Every time I've done it this way, the beer attenuated to at least 65% (AA), depending on the malt, yeast, etc. There is a difference between fermentability (which is fixed for a given mash) and apparent attenuation, which can vary for a particular wort, depending on the yeast strain, pitching rate, physiological state, fermentation temperature, wort O2 levels, etc. Maybe David is one of those brewers who pitches the yeast at the optimal rate while at high kraeusen! It works for me. >beta amylase >gets denatured quickly at 158F (and less quickly at 157F, and even less >quickly at 156F) and results in a less fermentable (more dextrinous) wort. I'm not sure if David even made this point, but I doubt the BA is completely denatured as rapidly as many seem to believe. The stuff doesn't just disappear all at once in an instant you know. In any case, a reasonably fermentable wort can be made by doing a single rest at 158F. [snip chart] >Note that these are for well-modified malt, but since virtually all >malt these days is well-modified, I'd say it is pretty applicable to >the discussion. I think malt quality varies more than you imply here. Brit pale ale malts are clearly more modified than typical continental pils malts (I've mashed a couple hundred pounds of each over the last 11 months and it's obvious). Munich malt also has a higher percentage of alpha 1-6 glycosidic bonds than other types of malt, making it inherently less fermentable than other malts, no matter how it's mashed. The point is, wort fermentability is dependent not only on the mash program but the choice of malt as well. (...and stop posting all this misinformation!) ;-) >Let's see if we can't summarize our two positions here, just for >clarity and put this discussion to rest: >Dave says that to increase fermentability, you need to mash longer >at 158F. I'll let David speak for himself here, but I'm not sure that's exactly how he put it. >I claim that he's wrong in this statement and that mashing >longer at 158F will not increase fermentability because after a very >short time at 158F the beta amylase in the wort will be denatured. Well, I can't help it, I just have to respond to this. I think you missed the point. Here's my interpretation of what David meant: IF you usually do a step mash with a short beta rest and a longer alpha rest (eg. 15 min at 149 then 30 min at 158) AND you're not satisfied with your FG (i.e. too high), you might TRY increasing the time of the mash, particularly by extending the length of the alpha rest (otherwise you might increase fermentability TOO much, if you increased the beta rest time). This should help decrease the FG some. I think the point was more that longer rests are likely to resolve this minor problem in many cases. I agree. Many texts recommend mash times that are too short, IMO. >I further claim that the wort will be no more fermentable after 2 hours >at 158F than it will be after only 1 hour at 158F. Maybe. That probably depends a lot on the quality of the malt, crush quality, etc., but I agree, if things go well, conversion of most mashes should be complete within about an hour. If not, longer rests will probably help! Tracy Return to table of contents
From: WineNBrew at aol.com Date: Tue, 9 Jul 1996 14:52:21 -0400 Subject: Re: White film in bottled beer...yuck or yum?! Dear Todd W Roat, Over the years there have been many of our customers who DID have the white film in their beer bottles. More than likely its just acetobacter flowers.....the beginnings of vinegar. Where'd it come from? Well, perhaps bottles that weren't 100% clean, a syphon hose or filler not quite clean, or the same with a draining faucet not taken apart and scrubbed, etc. etc. None of our customers has this problem anymore. Not for at least 20 years. Why? Because we don't use chlorine bleach anymore, nor any of the newfangled iodophors etc. Never have, never will! WHAT? ARE WE CRAZY? EVERYBODY USES THESE....EVERYBODY! Not us and not our customers (& we have a lot of 'em). OK! What do we do if we think we're such smartie-pants? We keep it fast, easy, fun, straightforward and simple. Scrub everything with lots of Arm & Hammer baking soda and warm water.....not soap of any kind. Then, after rinsing with lots of clear water.....Rinse with a stock solution of sodium metabisulfite. Let sit for 2-3 minutes. Rinse with lots more clear water. TA! DA! No problems. Period! Ever!....and no danger from splashed bleach on you or your clothes etc. Now, what can you do with THIS particular batch??? Easy! Give each bottle a quick twist back and forth. The film will break up, and settle to the bottom of your bottle. Don't age for a real long time. Pour slowly & enjoy this batch while slightly young. In the future use our measures and it won't happen again. Cheers! :) We've been in biz 24 years. Sandra & Craig Wine & Brew By You, Inc. Miami, Florida P.S. As a bribe, if you do follow our "best-ever" method, we'll send you a free copy of our malt-extract recipe to imitate the original New York Ballentine's XXX IPA. Just send us your snail-mail address. OK? OK! Return to table of contents
From: Mark Wallace/CAM/Lotus <Mark_Wallace/CAM/Lotus.NOTES at crd.lotus.com> Date: 9 Jul 96 14:59:56 EDT Subject: A WWW page! Category: Comments: Use doclink to get to the actual WWW page Return to table of contents
From: Steve Alexander <stevea at clv.mcd.mot.com> Date: Tue, 9 Jul 1996 15:01:05 -0400 Subject: re: Mashing Time - another point of view. David R. Burley writes ... >A wort held at a certain temperature in the saccharification range FOR LONG >ENOUGH TIME will naturally come to a certain, repeatable (assuming the same >malt >and water composition) composition because the alpha amylase will chew up all >the starch and the beta amylase will chew up all the intermediate starchy >residues, provided by the alpha amylase, it can, before it disappears. I think >we would all agree on this as a simplified, but adequate explanation of what >happens during the saccharification step. The variability of the composition of Assuming that there is any or enough AA and BA left to "chew up all the starch". I think that this is the only real point of contention with your 70C rest suggestion. >the wort is temperature dependent because the beta amylase is denatured at >temperatures in the so-called saccharification range (typically identified as >149 to 158 F). So while the beta amylase is producing fementable sugar during >the saccharification rest, it also is disappearing by an independent reaction. This isn't the 'typically identified' saccharification range from any source I've seen. Most often it's 60C(140F) to 70C(158) and around 149F(65C) is the middle value where several important optima occur, decidely NOT the low end. I can't recall seeing a commercial mash shedule that saccharifies outside 62C to 68C unless fungal source amylases are used. >It is a race to see whether the chopped up starch gets fully converted to sugar >before the beta amylase disappears or not. Since the beta amylase disappears at >the lower temperature more slowly, more of the starch intermediates get turned Have you examined the RATE of disappearance of BA (and AA) versus temperature and compared this with the rate of increased activity. I suspect not. Typically the rates of inactivation for enzymes increase by 10X to 100X per 10C increase, from memory the rates for grain amylases are around 20-30X per 10C. If you overshoot the temp by 2C, you'll get roughly 1/2 the total activity - assuming you mash till inactivation is nearly complete, which seems very likely at 70C. >into fermentable sugars than at high temperatures. As a result, the lower >saccharification temperatures produce the more fermentable wort IF it is held >at this temperature for LONG ENOUGH TIME.. True, and the other way of describing this situation, that you seem to be ignoring, is that if you mash at a HIGH ENOUGH TEMPERATURE, you will lack amylases before you adaquately hydrolyse your starches. As I've mentioned the effect of mashing 10C lower is roughly a 2X increase in time. The effect of mashing 10C higher is say a 25X decrease in enzymes availability once you are in the enzyme limited case. >My comments have ever ONLY related to those brewers who use Papazian's and >others' advice to use short sacharification times of 10 to 30 minutes or at >least less than an hour. Using short times will increase the likelihood of not >allowing the beta amylase to complete its job. As using high temperatures increases the likelyhood of preventing the BA from completing its job. > This is particularly true at >higher saccharification temperatures where the beta amylase is at a lower >concentration at any given time into the the saccharification rest. Being lower >in concentration ( even though the forward rate of saccharification is faster) >the OVERALL observed rate at the higher tempereature can be lower, DEPENDING >UPON 1) the type of malt and 2) the composition of the brewing water (liquor) >3) >The thickness of the mash. I'm not in favor of short sacch. times either, but it's quite likely that you won't see a significant amount of additional beta-amylase activity after the first 30' at 70C. Initial enzyme concentration counts, Calcium counts, thickness and particularly substrate concentrations count, lack of destabilizing metal ions count, but it's very hard argue that these can overcome the effects of the enzyme deactiviation vs temperature. >The type of malt is important since it controls the original concentration of >the enzymes. A highly converted malt like the British malts start out at a much >lower enzyme concentration than American or continental malts. American six row British pale ale malts have less diastatic power because of the kilning schedule (finals at 100C to 105C) not because of the degree of modification. Almost all malts today are highly modified including the diastatically powerful ones which kiln out around 85C. >different for different types of malt. The use of adjuncts will affect the >concentration of enzymes by simple dilution effects etc., etc. Because of the Wrong - another HB book momily. Grain adjuncts typically contribute substantially to the available beta-amylase content. All of the beta-amylase is present in a grain seed, unlike alpha-amylase which is synthesized during germination. Some BA is immediately available in ungerminated seed(~40%), some is immobilised and less active, but NOT inactive. The immobilized BA is released by the action of SH-proteinase enzyme. Immobilized BA can be released from unmalted adjuncts by either a protein rest with malted barley, assuming the proteinase is intact or by addition of artificial enzymes (e.g.papain). Both techniques have been used commercially. >The composition of the water is important since enzyme stability is dependent >upon calcium content as well as other ions. Generally pH and Calcium ions in >the >mash exhibit control over the rate of all the hydrolysis reactions and >apparently the rate of denaturization of the various enzymes, and importantly >the beta amylase. I would say 'importantly ALPHA-AMYLASE', not beta- !! Altho calcium improves the stability of beta-amylase to a point, the bigger effect is on stabilizing and increasing the activity level of Alpha-amylase. At 70C barley AA is quite unstable in low Ca+ environment. Further the activity of AA irreversibly lost when used in suboptimal Ca concentrations even at 60C. AA is actually classed as a metallo-enzyme because of the calcium requirement. > The thickness of the mash is important since the enzymes in question are more >stable in thicker mashes and also importantly, more stable in the mash than in >pure solutions on which many results have been reported. Also, the sugars >produced slow down the rate of conversion as the concentration goes up during >saccharification. A thick mash is supposed to have two positive effects. First it is said to act as a thermal buffer - or some such language. I think that this is from M&B Sci among other sources, but I don't really know what they are trying to say. It's obviously harder to get a consistent temperature in a thick mash, but that means both hot spots and cool spots. Perhaps they are trying to say that the intra-granular temperature won't rise as fast. I'm not sure. Anyone care to explain ? The second effect is substrate complex stabilisation. When the enzymes and substrate join or complex, then the enzyme may be more stable. This is the case for amyases - *BUT* - this is probably a small effect when it comes to normal mashes. BA and AA are both decidely much less stable in 'test' mash conditions which are often involve 10:1 water to grist ratios. I strongly suspect that the difference in stability between a 1qt/# (67% water) mash and 1.6qt/# (76% water) mash is a secondary effect. Useful, but not critical. Note that a thick mash only helps stability if it is full of substrate. If there are few 1-4 linked non-reducing ends for the BA to attack (for example if the mash is beginning and full of long amyloses & amylopectins) then there is less substrate to form stable enzyme+substrate complexes from. > In my original comment, I felt that because of the complexities outlined above >that it was far easier to hold longer at the chosen (by the HBDer) >saccharification temperature as a first step to solving a high OG problem than >to mess around with temperature and wort composition as some contributors >suggested. > >That's it. If confusion reigns now, let it! I don't deny that is is possible to mash at 70C, only that is is difficult, requires extra care and normally results in a high FG beer. I also admit that even with a 70C single infusion in cooler the effects of BA should be substantial. Since David Burley reports 75% apparent attenuation of a 70C mash (few mash details given) while more common experience indicates that a 68C mash can result in something around a 66% apparent attenuation, I think there is something here that requires explanation. Too bad the home gluco-spectrum test hasn't been invented yet to analyse David's wort. How about posting the mash details David ? pH, water chemistry, thickness. Method of temp control, measurement, mashing apparatus, malts details ... yield ... even yeast ... ? BTW - when was the last time you calibrated your thermometer ? (yes, I am still sceptical). Steve Alexander Return to table of contents
From: "Ray Robert" <Ray_Robert at bah.com> Date: 9 Jul 1996 15:07:46 U Subject: thermal contraction problem? Good Day Collective, I have one quick question: Do I risk permanent damage to my new brew kettle, a converted SS Keg (Thanks Wallie!), if I were to immerse it in an ice bath after a full boil? I did this with my enamel on steel pot without any visible damage. Would this hold true with the SS? John Palmer are you out there? I usually do the ice bath in conjunction an immersion chiller. Thanks, Robert ray_robert at bah.com Return to table of contents
From: John Chang <75411.142 at CompuServe.COM> Date: 09 Jul 96 15:29:42 EDT Subject: Fermentability Greetings, I just finished bottling a batch of pale ale brewed from a high-kilned English malt. Because I used 3 more pounds of malt than any previous batch (11 lbs total), I expected to get a higher OG than I got. OG:1042, FG:1010. (Sparge inefficiency?) I mashed at the higher end (158F) than my normal 150F with the expectation of creating a less fermentable (and hence, sweeter) wort (despite the latest HBD duiscussions on gelatinization at 140F). I adjusted my hops blindly, given an expected change in sweetness due to the new total amount of malt used and the higher mash temp. (apprx 12 AAU's for 5 gal) Question: In addition to mash temp, assuming complete conversion is achieved, what other variables can one use to control sweetness/maltiness? More malt? Yeast attenuation? - --------------------------------------------------------------------------------- - ------------------------------- This last batch was also pitched with a starter stepped up from yeast cultured from a bottle of Sierra Nevada Pale Ale. I would like to produce a clone using a yeast culture from a bottle of Chimay Belgian Ale, which I just got the pleasure to try last week. What an outstanding product!!! Would it be best to use the Dewolf-Cosyn's Belgian malt, English malt, or something else? - --------------------------------------------------------------------------------- - -------------------------------- Last question: Having only used the English pale malt in all of my five batches (went all grain right off the bat), what can I expect from American malt, Klages, etc. With respect to different types of malt, are there general guidelines to use in determining expected extract/efficiency? Thanks for the bandwidth and any responses. This hobby is one of the few I have undertaken that I find myself studying/reading/tinking about daily. Private email ok. TIA, John For those with experience in cloning this beer Question: do I ha Return to table of contents
From: "Tracy Aquilla" <aquilla at salus.med.uvm.edu> Date: Tue, 9 Jul 96 15:48:06 CDT Subject: Re: hi temp mash-source of sweetness? In Digest #2098: George_De_Piro at berlex.com (George De Piro) wrote: >Yes, Al was right in saying that I exaggerated when I said that >mashing at 158F for any length of time would yield a "barely >fermentable wort." I'm prone to hyperbole! It would yield a pretty >sweet beer, though. Maybe, but not necessarily. I hope you don't curse me George for continuing this thread based on your comment, but this brings up another issue that's bothered me for some time now. I agree with George that beers mashed at 158F tend to taste relatively sweet, depending on how they're handled during fermentation, but I don't think that dextrins contribute any flavor per se, and I'm not convinced that every beer mashed at 158 will necessarily taste sweet. Polysaccharides composed of greater than three (or is it four?) monosaccharide units have no flavor; they certainly aren't sweet. Sweetness is determined by residual sugars (i.e. small molecules), not dextrins or starches (NOTE: some proteins taste sweet too). Dextrins contribute to body and only indirectly influence flavor by altering texture. I'd be quite interested in any references indicating that dextrins taste sweet (I've been wrong before!). I think whether or not a beer tastes sweet depends more on wort composition, original gravity, the choice of yeast, and fermentation conditions than on the mash schedule itself, as the level of residual sugar is generally dependent on OG and the degree of attenuation, which is mainly dependent on the yeast strain and the conditions of the fermentation. Maybe now we can transform this one into a 'source of sweetness' thread? Tracy Return to table of contents
From: "Tracy Aquilla" <aquilla at salus.med.uvm.edu> Date: Tue, 9 Jul 96 16:30:49 CDT Subject: Re: Al & Dave's little tiff In Digest #2098: korz at pubs.ih.lucent.com wrote: >What do you want me to do? Should I get a sound byte from Pierre Celis >or Jean-Pierre Van Roy on this and put it on a Web page? This petty attitude is pretty annoying. I've experienced the same garbage myself recently and don't appreciate such a lack of personal respect. People other than relatively famous professional brewers ARE capable of making legitimate observations you know. For some reason, certain folks around here will only accept information as being legitimate if it comes directly from one of the so-called brewing 'gurus' (unless it's Greg Noonan). Problem is, even the gurus make mistakes (lots of them too!). Sorry Al, but training as a professional brewer does not a biochemist make. >What do you need to believe that mash temperature and not time determine >fermentability? We need facts based on data that can be examined by all. Lacking that, sometimes anecdotal evidence is all we have to go on. Most brewers I know agree that wort fermentability is a function of time and temperature, as well as the choice of malt. A one second mash at ANY temperature just don't work, Al! Time is a critical parameter. I'm bowing out of this thread now but I felt like David got a bum rap here and he deserves better treatment (everyone does). I believe this misunderstanding resulted from people misquoting David. If you must correct someone else's post, one would be wise to make certain to quote the source accurately. Tracy Return to table of contents
From: WineNBrew at aol.com Date: Tue, 9 Jul 1996 16:33:21 -0400 Subject: OOPS! A quick add-on re: cleaning OOPS! Our previous post re: cleaning with baking soda & sodium metabisulfite was exactly right for all your plastic equipment, but we left off the easiest way to clean really dirty beer bottles, glass carboys and wine bottles. Just put your bottles in a large waste basket or garbage can with lots of ammonia and water. Let 'em soak for a few hours. Look closely at them. Use a good bottle brush to scrub off heavy dirt particles. Then rinse well. Now use your baking soda and sodium metabisulfite solution as described in our last post. Voila! Finished. Now, your beer & wine bottles don't need to be cleaned each and every time, as long as you rinse them thoroughly right after pouring a glass. Store them upside down in a carton and the next time you fill 'em all you need do is give 'em a quick water rinse and fill. All done! Works perfectly! Guaranteed! Sandra & Craig Wine & Brew By You, Inc. Miami, Florida Return to table of contents
From: stafford at newport26.hac.com (Jack Stafford) Date: Tue, 9 Jul 96 13:59:48 PDT Subject: Mash temperature experiment With all the discourse on mash temperature and enzymes lately, I decided to try something differant first hand. Everything went very well except for spills and a sticky kitchen floor, then a stuck lauter that somehow got itself unstuck. This was a single step mash (80 min) in a zap-pap plastic bucket system. 10lb klagus malt, 1lb rice, 1lb corn, 1/2lb crystal 60L. This time around I did two things differant: I mashed at 150*F instead of 155*F. I made a very thick mash compared to my usual. The result was an OG of 1.064 in comparison to the customary 1.045 or so. On the third day of fermentation I took a gravity reading and it was 1.014 wow. It's in the secondary fermenter and the yeast is starting to flocculate. I could not believe it - 1.064 that's my highest gravity from all-grain to date. A lower mash temperature and a proper consistancy in the mash seemed to give a higher OG and it fermented quicker than the dickens. I'm not sure if this one was a fluke or not, I'll have to try it again. Thanks, you folks give me lots of tips and help me make better beer. Jack Costa Mesa, CA Return to table of contents
From: blades at airtime.co.uk (Liz Blades) Date: Tue, 9 Jul 96 21:28:48 BST Subject: Bug killers didest #2098 Hi, I've been following this thread with interest.The standard procedure here in the UK was to spray with good old fashioned washing up liquid. But since we're now part of the EU (or whatever it's called these days) It is now unlawful to use it as a bug killer!!!! and what I've just said is an offence. Incidentally it's unlawful because it got missed off a list of proscribed detterants.I've been using it for years and I'm not dead yet.....the same cannot be said for the aphids. Cheers Liz Blades Liz Blades Proprietor of Blades Home Brewery http://www.dmatters.co.uk/Blades/blades.html Return to table of contents
From: Carl Hattenburg <CHattenburg at Perstorp-us.com> Date: Tue, 9 Jul 1996 17:34:55 -0400 Subject: RE: HYPERBOLE >> George wrote: >>Subject: HYPERBOLE, watery mild brown ale >>like calibrate my thermometer (how anal, yeah go ahead and laugh...). Hmmm...and I've been using an ORAL thermometer! - - Carl H. (w)301.680.7276, (x)301.236.0134, (h) 301.942.3756, (e) CHattenburg at Perstorp-us.com Return to table of contents
From: "Craig Rode" <craig.rode at sdrc.com> Date: 9 Jul 1996 16:49:56 -0600 Subject: Yeast and ITBR? Subject: Time: 3:48 PM OFFICE MEMO Yeast and ITBR? Date: 7/9/96 Thanks for all the responses about re-using yeast. Upon re-reading my own post, I realized that I wasn't being quite clear. What many of you thought I was asking was 'Can I recycle the yeast from my carboy?' When what I meant to ask was "Can I recycle the yeast from my bottle?'. In other words, suppose that when it's time to get my starter going, instead of using a smack-pack, I open 3-4 bottles of existing homebrew...pour that into a couple of beer glasses, and dump the dregs (which I normally swig) into the starter? How much am I risking infection? "Is Their Beer Ruined" or "There Oughta Be a Law"...Yesterday I was in a microbrewery that shall remain un-named. (You know who you are!) I was handed a 'new' beer they were trying out. Im my opinion, it was the best beer they had ever made, and I bought 2 six packs on the spot. Then the brewer tells me "This wasn't what the owner had in mind. We dumped 300 gallons of it into the sewer." AAAARRRRRGGGGHHHHH!!!!!!!!!!!!! See what rigorous attention to styles makes people do? Craig Return to table of contents
From: "Goodale, Daniel CPT 4ID DISCOM" <GoodaleD at HOOD-EMH3.ARMY.MIL> Date: Tue, 9 Jul 1996 17:20:00 -0500 Subject: Beer in Spaaace Al writes: >Check the diffusion rates through semi-permiable membranes and the rate >of production of CO2 during fermentation. I am quite sure that they >would be at least an order of magnitude off, maybe two or three. Probably so. Might be able to increase the efficiency by a negative pressure on one end. A better way is to radically alter the carboy design to increase surface area of the membrane and decrease the distance the CO2 has to travel. The logical conclusion; lung shaped carboys. They say that the surface area of the human lungs can cover a tennis court. If our semipermeable membrane had that or greater surface area it may be able to handle the CO2 production of fermentation. This would also eliminates the chance that a huge bubble of CO2 would sit in the middle of the carboy and not come in contact with the membrane. Does anybody know if CO2 bubbles produced in fermentation have a charge (or be given one)? Perhaps we could draw them out electostatically? Daniel Goodale (yes that is my real name) The Biohazard Brewing Company I like to think of myself as a chemical super-freak. Return to table of contents
From: Jeff Hewit <jhewit at erols.com> Date: Tue, 9 Jul 1996 19:19:42 -0400 (EDT) Subject: Skunked Beer I recently brewed a fairly highly hopped ale - IBU's from 59 to 66, depending on whose method you use. I bottled the batch in brown bottles, as usual, except for one clear Corona bottle. I put this on the window sill of my kitchen, which gets a decent amount of sun, plus is under a florescent light that is on 24 hours a day. After about three weeks, I opened the clear bottle along with a brown one. What a difference! Up until now, I wasn't really sure what skunked beer was supposed to be like. I have had experience with skunks, but couldn't quite translate that experience to drinking beer. The skunk was definitely in this beer. However, it was quite drinkable - not good, but drinkable. And, the smell and taste reminded me of Heineken. As others have recently noted here, Heineken has a skunky smell. To my previously untrained senses, the smell of Heineken was not strong enough to evoke an immediate recollection of brining my dog home after an altercation with one of those black and white critters. Now Heineken, which is often the best available, will never taste the same. I have heard others mention beer that was so skunked that it was undrinkable. Anyone know how long this takes? I could do another experiment with my next batch, but I really hate to sacrifice good homebrew, even in the name of science. Brew On! Return to table of contents
From: korz at pubs.ih.lucent.com Date: Tue, 9 Jul 96 19:17:31 CDT Subject: Burley vs. Korzonas David writes: >AlK - Please stop paraphrasing me and what other people have written >paraphrasing me. I think this adds to the confusion, because I think that's all >this is. A misinterpretation of my comments. Go back and read all of my >comments on this subject for yourself. I have said from the beginning that high >temperature saccharifications give higher FG worts etc. I have even said on >more >than one occasion that we all agree on the basics. In the beginning, you said (not paraphrasing): >Reading Domenick Venezia's trials (and tribulations) on using oxidation to try >get to lower FG is in line with some other recent comments I have read here >from >brewers who are unhappy with high FG brews. In some cases it may simply be >that >they started with a high OG wort and if this were diluted to the 1.05 region, >would deliver a "normal" FG in the 1.01 range. > >However, Domenick and some of the other brewers are probably experiencing >either a poorly attentative yeast - a genetic trait, in most cases, and >unchangeable OR most likely, in the case of all grain brews, they are holding >at >a high a temperature ( say 158-160) for too SHORT a time during the >saccarification stage. This is your initial statement and it is wrong. Increasing the time at 158-160F will not decrease the FG. This is what started this whole, long, very tiring thread. Back to your recent post: >PROPERLY CARRIED OUT, saccharifications at higher temperatures will produce a >less fermentable wort than at lower temperatures. That was never the problem. >The problem is when one gets HIGHER THAN EXPECTED FG, one may increase the hold >time during the saccharification step to make sure the beta amylase has done >all >it can do. This is easier to do than changing mash schedules and mash >compositions. >Short saccharification times can lead to higher than expected FG's since the >beta A is not given the chance to convert all the product from the alpha >amylase, particularly at the higher temperatures where the beta amylase >concentration (at any time t) is lower than at the same time t at a lower >temperature and the OVERALL rate of sugar production is lower. The alpha >amylase >products arise faster, because the rate is greater at the higher temperature. >Conceivably, under certain circumstances of mash composition and temperature >schedules all of the starch could be converted, but not all of the >intermediates >converted to sugar at the same time the starch disappears, particularly if the >beta amylase content is low.. This again is wrong. Steve Alexander, weeks ago, posted that alpha amylase is isolated (i.e. beta amylase is compleatly denatured) within 15 minutes at 158F. At no time beyond 15 minutes is there any more beta amylase activity. No, to change fermentability, if you are mashing at the high-end of the amylase range, it is not possible to decrease the FG without lowering the mash temperature on a subsequent batch. >Thanks for the tip on 80 cols vs say 60. Maybe this explains why people don't >clip me and choose to paraphrase me. No, I believe that people paraphrase you because your posts are so long. More is not always better. I was going to go on and comment point-by-point on the rest of your post, but it serves little purpose. Jeff Renner's post started me thinking about the length of my own posts. In trying to find your original post, I started around issue 2084 and started working backwards. I was shocked at the amount of bandwidth wasted on this topic and was irritated by the gobs of text I had to plough through. Then this thought struck me... other readers are probably just as irritated by my long posts as I was having to sift through yours. It's as if this is the Al and Dave Digest and not the Homebrewer's Digest. I pledge to try to keep my paraphrasing, quoting and posts to a minimum and I think that the HBD would be well-served if you did the same too, Dave. If we ever get onto a thread like this again, we should take the blasted topic off-line, work it out and post a summary! I also "shoot from the hip" all too often. Dave, you know you do too. Let's all try to verify our info before we post? It will save a lot of correcting by ourselves and others in subsequent posts... Al. Al Korzonas, Palos Hills, IL korzonas at lucent.com Copyright 1996 Al Korzonas Return to table of contents