Thursday, February 26, 2009

Homebrew Digest #5514 (February 26, 2009)

HOMEBREW Digest #5514 Thu 26 February 2009


FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
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Contents:
RE: Lot analysis data for Weyermann malts? ("Mike Bennett")


* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
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----------------------------------------------------------------------


Date: Thu, 26 Feb 2009 12:04:53 -0800
From: "Mike Bennett" <mjb at efn.org>
Subject: RE: Lot analysis data for Weyermann malts?


Kai Troester <kai at braukaiser.com> wrote:

> Does anyone know of a source where I can buy bags of Weyermann
> malt AND get lot analysis data for them?

I've had EXCELLENT customer service and support from

F. H. Steinbart
234 SE 12th Avenue
Portland, Oregon 97214 USA
503.232.8793
http://www.fhsteinbart.com

Their retail prices are a little high IMO, but it could be because I'm so
used to paying wholesale as a pro brewer.

> I have been buying my malt from Crosby Baker through my LHBS.
> While I?m willing to pay the premium for this excellent German
> malt (I pay ~$60 for the 55 lb bag) I don?t understand why I
> cannot get the lot analysis data if I?m paying this price.

I've had nothing but bad experiences with C&B in the past. Considering the
service That I've gotten from them as a pro, I'm not surprised they didn't
hang up on you as soon as they found out you were a home-brewer.

> Granted a home brewer should not have to worry about detailed
> data like this but let me be the judge of this.

You may be disappointed when you finally get your lot analysis, at least
with the specialty malts. 98% of the time, they are little more than a
color analysis.

- --
Mike Bennett
Professional Brewer (retired)
St. Barts (Home) Brewing
mjbennett69<at>gmail.com


------------------------------
End of HOMEBREW Digest #5514, 02/26/09
*************************************
-------

Wednesday, February 25, 2009

Homebrew Digest #5513 (February 25, 2009)

HOMEBREW Digest #5513 Wed 25 February 2009


FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
Digest Janitor: pbabcock at hbd.org


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***************************************************************


Contents:
Malt Analysis (Thomas Rohner)
Mash temperature calculations (specifically "slaking heat") ("Bill Pierce")


* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* The HBD Logo Store is now open! *
* http://www.hbd.org/store.html *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* Beer is our obsession and we're late for therapy! *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *

NOTE: With the economy as it is, the HBD is struggling to
meet its meager operating expenses of approximately $3400
per year. If less than half of those currently directly
subscribed to the HBD sent in a mere $5.00, the HBD would
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spare for next year. Please consider it.

As always, donors and donations are publicly acknowledged
and accounted for on the HBD web page. THank you


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JANITORs on duty: Pat Babcock (pbabcock at hbd dot org), Jason Henning,
and Spencer Thomas


----------------------------------------------------------------------


Date: Wed, 25 Feb 2009 13:07:14 +0100
From: Thomas Rohner <t.rohner at bluewin.ch>
Subject: Malt Analysis

I think it would be a good idea for a maltster to put the lot data of
the products on their Website. This way the ones interested in the data
could get it without the maltster having to reply phone calls or emails.
I'm also using Weyermann almost exclusively. (the easiest to get around
here)

Cheers Thomas


------------------------------

Date: Wed, 25 Feb 2009 11:26:01 -0500
From: "Bill Pierce" <BillPierce at aol.com>
Subject: Mash temperature calculations (specifically "slaking heat")

Thanks to all for the replies to my earlier question about the
thermal calculations for accurate mashing temperatures. It takes me
some time to digest all of the information (I'm not a scientist by
training), and of course brewing is not the only thing in my life.

As a couple of people pointed out, the difference between the
results of my experiment with hot water and the calculated thermal
mass of my converted keg mash tun based on the heat capacity of 304
stainless steel is due to the fact that the keg is not full; only a
portion of it is in direct contact with the strike water. No doubt
a truly accurate formula would have to take the geometry of the
vessel into account, as well as the thermal conductivity of the
vessel's material as it conducts and radiates heat into the
environment. I was also supplied with an interesting article by Dan
Morey that I had not seen before, which includes formulas for
predicting the temperature drop over time when mashing. My thoughts
on that subject are that additional factors such as humidity and
wind velocity (if mashing outdoors) have an influence as well.

I'll retreat to a position that the best way to determine a vessel's
thermal mass is to calculate it on the basis of measurement by
experiment. It's simple enough to do, and I trust my formula:

ThM = ((Ts-Td)*2.08635*Vw)/(Td-Tm)

Where:
ThM = Thermal mass of vessel (lbs. or kg)
Ts = Strike water temperature (degrees F or C)
Td = Water temperature achieved after settling (degrees F or C)
Vw = Volume of strike water (quarts or liters)
Tm = Mash tun temperature (degrees F or C--typically ambient
temperature)

The formula works for metric brewers as well, as long as they use
metric values throughout and omit the 2.08635 coefficient, which
converts the water volume in quarts to pounds. Do the measurement
with water only; I have eliminated the grain variables from the
equation.

However, several people pointed out one other variable I had not
considered, nor does this seem to be mentioned in the standard
homebrewing literature. This is the notion of "slaking heat";
apparently the hydrolysis of the malt starches is an exothermic
reaction that releases measurable heat. Various professional
brewing references, including "Brewing: Science and Practice" by
Briggs, Boulton, Brookes and Stevens, include the following formula:

F = (St+RT+0.5h)/(S+R)

Where:
F = Final temperature of mash after settling
S = Specific heat of malt
t = Temperature of malt
R = Water/grain ratio of mash
T = Strike water temperature
h = Slaking heat of malt

Solving the equation for h (slaking heat), results in this formula:

h = -2*(R+S)*(((St+RT)/(R+S))-F)

The literature includes a table of slaking heat based on a mash
temperature of 150 degrees F. If I plug this temperature and my own
typical values (malt temperature of 70 F, strike water at 160 F, 0.4
for the specific heat of malt, 1.35 quarts per pound water/grain
ratio) into the formula, I arrive at a the same value (18.8
gram-calories per degree F) as the table. Using the formula and
converting 18.8 gram-calories/degree F) to the value used in my
strike water temperature formula, the result is 0.07460 BTUs (metric
brewers will excuse me here). In a hypothetical mash with 10 lbs.
of grain, again at a water/grain ratio of 1.35 qts/lb, the result is
a total of 111.45 BTUs at 150 degrees F.

The effect on the calculated strike water temperature is
significant, a total of 4.0 degrees F in my hypothetical example.
This is consistent with what Briggs et al. report. However, as I
have said, this is nowhere mentioned in the standard homebrewing
literature nor apparently included in the software most homebrewers
use.

There is a suggestion that the slaking heat is offset by the thermal
mass of the mash tun. Indeed if I eliminate both the vessel's
thermal mash and the slaking heat from my strike water calculation
formula, the difference is reduced to 0.8 degrees F, likely within
the measurement resolution of most thermometers.

Still, it seems there is considerable margin for error in the
homebrew strike water temperature formulas, and those of us who wish
to be precise (some would say anal) about these matters are
disturbed. Is the slaking heat of a typical homebrew mash as great
as 4 degrees F as the formulas and literature suggest, or is this
largely much ado about nothing?

Any input from the technically minded would be greatly appreciated.

Brew on!

Bill Pierce
Cellar Door Homebrewery
Burlington, Ontario

------------------------------
End of HOMEBREW Digest #5513, 02/25/09
*************************************
-------

Tuesday, February 24, 2009

Homebrew Digest #5512 (February 24, 2009)

HOMEBREW Digest #5512 Tue 24 February 2009


FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
Digest Janitor: pbabcock at hbd.org


***************************************************************
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***************************************************************


Contents:
Metric Inches (Stephen Neilsen)
Lot analysis data for Weyermann malts? (Kai Troester)


* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* The HBD Logo Store is now open! *
* http://www.hbd.org/store.html *
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* * * * * * * * * * * * * * * * * * * * * * * * * * * * *

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JANITORs on duty: Pat Babcock (pbabcock at hbd dot org), Jason Henning,
and Spencer Thomas


----------------------------------------------------------------------


Date: Tue, 24 Feb 2009 20:41:52 +1100
From: Stephen Neilsen <stephen.neilsen at gmail.com>
Subject: Metric Inches

Oh dear...well of course in a constantly changing world (I am only
talking about increasingly accurate measurement) we have changes.
Anyway on a Brew (ish) related topic it has been said that the inch
was the measure of 5 corns of barley, placed end to end.
There was also that story about Jim Morrison of The Doors, but that is
for less sober forums...

SN in Kanbeera


------------------------------

Date: Tue, 24 Feb 2009 14:22:58 -0500
From: Kai Troester <kai at braukaiser.com>
Subject: Lot analysis data for Weyermann malts?

Does anyone know of a source where I can buy bags of Weyermann malt
AND get lot analysis data for them?

I have been buying my malt from Crosby Baker through my LHBS. While
I?m willing to pay the premium for this excellent German malt (I pay
~$60 for the 55 lb bag) I don?t understand why I cannot get the lot
analysis data if I?m paying this price.

Granted a home brewer should not have to worry about detailed data
like this but let me be the judge of this.

I have contacted Weyermann and Crosby Baker about this. Weyermann told
me that I?m ordering too little to get the data from them. Something I
understand as I don?t think they should be responsible to handle the
inquires from all the home brewers who want data for their bags of
malt. But Crosby Baker as the importer should be able to get this data
from Weyermann and give it to me on request.

I'd really hate to stop buying malt from my LHBS just because of this.

Kai


------------------------------
End of HOMEBREW Digest #5512, 02/24/09
*************************************
-------

Monday, February 23, 2009

Homebrew Digest #5511 (February 23, 2009)

HOMEBREW Digest #5511 Mon 23 February 2009


FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
Digest Janitor: pbabcock at hbd.org


***************************************************************
TODAY'S HOME BREW DIGEST BROUGHT TO YOU BY:

Sponsor The Home Brew Digest!
Visit http://www.hbd.org/sponsorhbd.shtml to learn how

Support those who support you! Visit our sponsor's site!
********** Also visit http://hbd.org/hbdsponsors.html *********

DONATE to the Home Brew Digest. Home Brew Digest, Inc. is a
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FAQ at http://hbd.org for details of this status). Donations
can be made by check to Home Brew Digest mailed to:

HBD Server Fund
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or by paypal to address serverfund@hbd.org. DONATIONS of $250
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amount are considered paid advertisement, and may be deductible
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tax professional, then see http://hbd.org for available
sponsorship opportunities.
***************************************************************


Contents:
natural units (steve alexander)
slaking heat ("Spencer W. Thomas")


* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* The HBD Logo Store is now open! *
* http://www.hbd.org/store.html *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* Beer is our obsession and we're late for therapy! *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *

NOTE: With the economy as it is, the HBD is struggling to
meet its meager operating expenses of approximately $3400
per year. If less than half of those currently directly
subscribed to the HBD sent in a mere $5.00, the HBD would
be able to easily meet its annual expenses, with room to
spare for next year. Please consider it.

As always, donors and donations are publicly acknowledged
and accounted for on the HBD web page. THank you


Send articles for __publication_only__ to post@hbd.org

If your e-mail account is being deleted, please unsubscribe first!!

To SUBSCRIBE or UNSUBSCRIBE send an e-mail message with the word
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http://hbd.org.

LOOKING TO BUY OR SELL USED EQUIPMENT? Please do not post about it here. Go
instead to http://homebrewfleamarket.com and post a free ad there.

The HBD is a copyrighted document. The compilation is copyright
HBD.ORG. Individual postings are copyright by their authors. ASK
before reproducing and you'll rarely have trouble. Digest content
cannot be reproduced by any means for sale or profit.

More information is available by sending the word "info" to
req@hbd.org or read the HBD FAQ at http://hbd.org.

JANITORs on duty: Pat Babcock (pbabcock at hbd dot org), Jason Henning,
and Spencer Thomas


----------------------------------------------------------------------


Date: Mon, 23 Feb 2009 05:24:04 -0500
From: steve alexander <steve-alexander at roadrunner.com>
Subject: natural units

Greg Lehey notes ,

> So what time units do you use?
>
> In any case, this is incorrect. The metric system was developed with
> 'time' based on decimal divisions of the solar day. The time you talk
> about is in such universal usage that it ovverrode the more rational
> metric approach, which was never introduced as part of the metric
> system.
>
Not quite. There was a French decimal day in use for just a few years
before the metric convention, but it was suspended about the same time.
The original metric system had no time unit ! The seconds defined as
1/86400 of the mean solar day was adapted in 1954 as the original metric
time unit, but the second was used w/o complete definition before that.

The second may be almost universal but even in scientific journals we
see time in minute, hours, days etc - non-metric units. The 100kph
signs on the roadside aren't metric for the same reason.

>> This is the system that was developed with a 'length' based on a bad
>> estimate of the distance from equator to pole of some mostly
>> harmless planet, ...
>>
>
> Well, again no. It was originally conceived with a length based on
> the length of a pendulum with fixed period. That definition lasted
> about 10 months, to be replaced by the one you mention, which lasted 8
> years, to be replaced by yet another one in December 1799.
>
> In any case, this is the definition of the unit, not the usage. Using
> the technology of 220 years ago, what more elegant unit would you
> propose?
>
The pendulum (~0.93 meter) was adopted by the French National Assembly
months before the French Academy of Sci chose 10^-7 earth quadrants - so
there is a question if whether the pendulum was ever part of "the metric
system". A provisional meter estimated at 10^-7 quadrants was
developed in 1793, and this was replaced in 1799 by a bar meant to be
the same 10^-7 quads but now acting as the (then) official definition.

>> where temperature is expressed in units based on the phase change of
>> H2O at some ambient pressure
>>
>
> ... directly related to its most normal usage. Again, how does this
> differ from other definitions of the day? You omit to point out that
> the definitions have long since been replaced by corresponding
> definitions based on absolute physical constants.
>

No not physical constant unfortunately. The original silly units have
just been replaced with new silly units of about the same size.
Instead of a second defined by the 1/86400 of an earth day we have a
second defined as several zillion cycles of the hyperfine oscillation of
Cesium where the number is mumbo-jumbo for "almost the old second" ....
tho' later papers suggest the Cs must be in the ground state at absolute
zero, and further conditions will be added as needed. The standard is
fluid ! The constants change. This is from their legacy as poorly
defined quantities.

I'll give props to to the current temp definition, but the mole has
issues resolved in the 1980s, the second has defintional problems
related to the state of cesium133. The meter is dependent on the lousy
second. Sorry Greg, but these "physical constants" are destined to
continue changing just as they have over the past 40 years.

AJ adds ....
> Temperature is defined in terms of absolute 0 and the triple point of
> water neither of which is dependent on pressure. The temperature scale
> (ITS-90) is, thus, defined in terms of fundamental physical constants.
>
This was adopted in 1967, where a Kelvin is 1/273.16 of the
thermodynamic temperature of the triple point of water. So why would
absolute zero and the triple pt be divided into 273.16 units of measure
? B/c it refers back to the Celsius unit which preceded it obviously
and they again tried to make 1K "almost the same" as 1C. A foolish if
practical consistency.
> The meter is defined as the distance light travels in a vacuum in
> 1/299792458 sec and thus related to a fundamental physical constant -
> the hyperfine transition of the outer electron in the cesium atom in a
> field free environment.
>

That's the current meter definition, but before that a certain number of
wavelengths of something or other.
and this definition is a great example of the problem.

meter = C * 1/299792458 sec.
second = 9,192,631,770 Periods transition between the two hyperfine
levels of the ground state of the caesium-133 atom.

So to make this definition come out to these nice integer values, which
"constant" has changed ? (the meter in this case). Before that the
second was tweaked to the cesium periods. Every time the definition
changes the unit changes slightly. The constants are inconstant. A
meter is exactly the length the CGPM thinks it should be this decade,
but it's always close enough to the old value to avoid everyday
problems; yet different enough to bugger-up old textbooks and tables.

Then we have the amp ,volt, coulomb system which is IMO has inferior
definitions to the gaussian-cgs statvolt statamp, esu system but .. The
seven base units should overconstrain the dimensions too, and this shows
up in the derived electromagnetic units I think.

> That brings us to the kilogram. [...] As
> this is disquieting to scientists there is effort afoot to tie the
> kilogram to a fundamental physical constant (which will probably be
> Planck's constant).
>

But we can construct fundamental units from some of the very basic
physical constants - the unit charge, planks constant, gravitational
constant, c - there is no need for the silliness of committee
definitions for units any longer. You can't revise the definition of
gravitational constant or the unit charge.

To answer Greg's questions, I'm partial to the systems called "Plank's
units" here
http://en.wikipedia.org/wiki/Natural_units

-S

------------------------------

Date: Mon, 23 Feb 2009 10:07:50 -0500
From: "Spencer W. Thomas" <hbd at spencerwthomas.com>
Subject: slaking heat

Slaking heat appears to have been first mentioned in the HBD in 1992:

http://hbd.org/hbd/archive/973.html#973-25
http://hbd.org/hbd/archive/1036.html#1036-1

These references include no explanation. It came up again in 1995,
1997, 1998, 1999, but then dropped off the radar until now.

I found an abstract of a 1910 article in the J Inst of Brewing on the
topic, which seems to be an early description of the concept with
experimental values derived:

The Specific Heat of Malt and the Calculation of the "Initial Heat"
of the Mash. H. T. Brown. (J. Inst. Brewing, 1910, 16,
112-129.)--The author,
in a previous communication on this subject (J. Inst. Brewing, 1899,
5, 335), had
assumed that dry malt must be assigned a specific heat of at least
0.52 (instead of
the value usually given of 0.42), from the data he obtained when
experimental
mashes were made, if allowance be made for the whole of the heat
evolved when dry
malt is mixed with cold water-"slaking heat." More recent work shows
that
0.38 is the true value for dry malt, rising to 0.41 for malt
containing 6 per cent.
water, and reasons are given for showing that in reality only one
half the value of
the " slaking heat " is available when malt and hot water are mixed.
This slaking
heat varies in a direction inverse to the moisture content of the
malt. The amended
formula for the calculation is appended :

I = (St+RT)/(S+R) + 1/2 H/(S+R)

S =specific heat of the malt (0.38 if dry, otherwise obtainable frem
the table).
t =temperature of the malt.
R = weight of'water corresponding to unit weight of malt.
T =temperature of the water.
H=the slaking heat of the malt in cold water expressed in
grm.-calories F. (obtained from table).

I = the initial temperature of the mash.

I also found a more recent mention in a Google Book entry:
http://preview.tinyurl.com/c34mh2

Brewing: Science and Practice
By Dennis E. Briggs, Chris A. Boulton, Peter A. Brookes, Roger Stevens
Edition: illustrated
Published by CRC Press, 2004
ISBN 0849325471, 9780849325472


=Spencer in Ann Arbor

------------------------------
End of HOMEBREW Digest #5511, 02/23/09
*************************************
-------

Sunday, February 22, 2009

Homebrew Digest #5510 (February 22, 2009)

HOMEBREW Digest #5510 Sun 22 February 2009


FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
Digest Janitor: pbabcock at hbd.org


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***************************************************************


Contents:
Re: Metric ? ("Greg 'groggy' Lehey")
Metric System ("A.J deLange")
Fingers and toes (Kevin Elsken)
2009 Coconut Cup Results (Scott Graham)


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----------------------------------------------------------------------


Date: Sat, 21 Feb 2009 16:39:19 +1100
From: "Greg 'groggy' Lehey" <grog at lemis.com>
Subject: Re: Metric ?

On Friday, 20 February 2009 at 15:52:08 -0500, steve alexander wrote:
> Kevin Elsken says ...
>> Subject: Thermal Mass
>>
>> First of all, for goodness sakes man, come over to the dark side and
>> just use the metric system! It is just so much better and easier.

[rearranged for sake of argument]

> This is the system that was developed ... with 'time' based on the
> planet's solar day divided by 86400 ((according to the Sumerian
> number system and time units - lost culture of the same planet))

So what time units do you use?

In any case, this is incorrect. The metric system was developed with
'time' based on decimal divisions of the solar day. The time you talk
about is in such universal usage that it ovverrode the more rational
metric approach, which was never introduced as part of the metric
system.

> This is the system that was developed with a 'length' based on a bad
> estimate of the distance from equator to pole of some mostly
> harmless planet, ...

Well, again no. It was originally conceived with a length based on
the length of a pendulum with fixed period. That definition lasted
about 10 months, to be replaced by the one you mention, which lasted 8
years, to be replaced by yet another one in December 1799.

In any case, this is the definition of the unit, not the usage. Using
the technology of 220 years ago, what more elegant unit would you
propose?

> where temperature is expressed in units based on the phase change of
> H2O at some ambient pressure

... directly related to its most normal usage. Again, how does this
differ from other definitions of the day? You omit to point out that
the definitions have long since been replaced by corresponding
definitions based on absolute physical constants.

> ... many of the units are divided by powers of - and all expressed
> in a base - determined by the typical number of flanges on the
> forepaws of a primate species.

Of course. It was designed for the convenience of this specific
primate species. And the choice of the original definitions of the
units has nothing to do with their usage. It was dependent both on
the technology available at the time and the need to avoid
all-too-drastic changes. You might just as well say that the unit of
length is 10000/254 inches.

Compare this to units which vary from one place to the other, such as
pints and quarts--one of the most important motivations for the
introduction of the metric system--and artificial and obfuscatory
units which make no sense.

Serious questions:

- What is heavier, a pound of gold or a pound of feathers?
- What does the constant 68.5 have to do with ppppg?
- What does the constant 57.0 have to do with ppppg?

> Easier - yes if you count on your fingers and toes.

Even easier if you leave your toes out of it. But it also depends on
how you count on your fingers. I do so in binary (one hand: 0-31; 2
hands: 0-1023).

> Better -- if I laugh any harder beer comes out my nose.

Is there a way to exploit that commercially?

Greg
- --
Finger grog at Freebsd.org for PGP public key.
See complete headers for address and phone numbers.

------------------------------

Date: Sat, 21 Feb 2009 08:10:25 -0500
From: "A.J deLange" <ajdel at cox.net>
Subject: Metric System

Temperature is defined in terms of absolute 0 and the triple point of
water neither of which is dependent on pressure. The temperature scale
(ITS-90) is, thus, defined in terms of fundamental physical constants.

The meter is defined as the distance light travels in a vacuum in
1/299792458 sec and thus related to a fundamental physical constant -
the hyperfine transition of the outer electron in the cesium atom in a
field free environment.

That brings us to the kilogram. It is the mass of a lump of metal
called the International Prototype Kilogram (IPK) in a lab outside
Paris. As the mass of an object is proportional to the amount of
matter in it the mass of the IPK changes over time as it wears (though
the IPK is handled very seldom) and adsorbs atoms from the atmosphere
(it is cleaned periodically to reduce this). Nonetheless, the unit of
mass is NOT derived from a basic physical constant. It is the only one
of the SI units that is currently based on an artifact (the IPK). As
this is disquieting to scientists there is effort afoot to tie the
kilogram to a fundamental physical constant (which will probably be
Planck's constant).

So while the metric system was originally artifact based (meter
1/10,000,000 of the distance from the pole to the equator, kilogram
the mass of a liter of water, temperature the ice point of water at
sea level...) it is no longer so with the exception of the kg. Today,
despite the US's stubborn refusal to join the rest of the world and
adopt the metric system we still benefit from it as the inch has been
redefined to be precisely 2.54 cm (as opposed to 1/36 the distance
from Henry's nose to his thumb), the pound exactly 0.45359237 kg and
so on. Indeed furlongs, firkins, pottles and all such other quaint
units of measure can be tied to the basic SI units by adoption
(usually by some body whose authority is accepted) of conversion
algorithms which are usually just scaling factors.

A.J.


------------------------------

Date: Sun, 22 Feb 2009 09:33:09 -0500
From: Kevin Elsken <littleboybrew at verizon.net>
Subject: Fingers and toes

Steve wrote:

> Easier - yes if you count on your fingers and toes. Better -- if I
> laugh any harder beer comes out my nose.

Well...I do count on my fingers and toes. Which makes it better for me!


------------------------------

Date: Sun, 22 Feb 2009 13:51:16 -0500 (EST)
From: Scott Graham <grahams at cs.fiu.edu>
Subject: 2009 Coconut Cup Results

The 2009 Coconut Cup was another rousing success thanks to everyone's
support. With 244 we really appreciate everyone's help!

Special thanks go to our out of town judges--Glenn Exline (SAAZ), Nelson
Crowle (DBG), Andy Rodusky (PBD), Joe Peters (PBD), Paul Blatz (PBD),
Blake Balsara (PBD), and Marshall Silk (FLAB)--as well as our out of town
stewards, the incomparable Dani Exline (SAAZ) and Squeaky O'Connor (PBD).
Many thank to the dedicated MASH members and their beer-loving friends who
assisted with the judging, stewarding, and logistics.

Additional thanks go to our Sponsors, the Titanic Brewery & Restaurant,
Gordon Biersch, Briess, Wyeast, White Labs, Dogfish Head, Northwestern,
and Sierra Nevada.

The results of the 2009 Coconut Cup are posted at
http://www.miami-homebrew.org/coco-cup/CocoCup09_Results.html

Congratulations to the winners and to the winning club, Tampa Bay BEERS.
We'll have the Cup engraved soon and it will return to its permanent home
above the bar at the Titanic Brewery & Restaurant in Coral Gables.

We look forward to seeing your brews at next year's Coconut Cup!

Scott Graham
Coconut Cup Judge Coordinator
[1159.9, 169.3] Apparent Rennerian


------------------------------
End of HOMEBREW Digest #5510, 02/22/09
*************************************
-------

Friday, February 20, 2009

Homebrew Digest #5509 (February 20, 2009)

HOMEBREW Digest #5509 Fri 20 February 2009


FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
Digest Janitor: pbabcock at hbd.org


***************************************************************
TODAY'S HOME BREW DIGEST BROUGHT TO YOU BY:

Sponsor The Home Brew Digest!
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amount are considered paid advertisement, and may be deductible
under IRS rules as a business expense. Please consult with your
tax professional, then see http://hbd.org for available
sponsorship opportunities.
***************************************************************


Contents:
RE; Heat calculations and thermal mass / Slaking Heat (Fred L Johnson)
11th Annual UKG Drunk Monk Challenge (John Kleczewski)
Re: Thermal Mass (Kai Troester)
Metric ? (steve alexander)


* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* The HBD Logo Store is now open! *
* http://www.hbd.org/store.html *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* Beer is our obsession and we're late for therapy! *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *

NOTE: With the economy as it is, the HBD is struggling to
meet its meager operating expenses of approximately $3400
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----------------------------------------------------------------------


Date: Fri, 20 Feb 2009 08:40:53 -0500
From: Fred L Johnson <FLJohnson52 at nc.rr.com>
Subject: RE; Heat calculations and thermal mass / Slaking Heat

Matt:

Many thanks for your post regarding slaking heat of malt during the
mash-in process. I had NEVER heard of this and will update my
spreadsheet to include this.

I noticed Malting and Brewing Science got the formula correct,
whereas Brewing: Science and Practice screwed it up.

Great post!

Fred L Johnson
Apex, North Carolina, USA

------------------------------

Date: Fri, 20 Feb 2009 08:28:07 -0600
From: John Kleczewski <john.kleczewski at gmail.com>
Subject: 11th Annual UKG Drunk Monk Challenge

The Urban Knaves of Grain announce that the Drunk Monk Challenge 2009
will soon be upon us! The competition is sanctioned by the American
Homebrewers Association, and is a qualifying event for MCAB and the
Midwest Homebrewer of the Year circuit.

The competition is scheduled for March 13 and 14, 2009, to be held at
Walter Payton's Roundhouse in Aurora, IL. As in previous years, the DMC
features the Menace of the Monastery, a special category consisting of
styles which are monastic in origin: Belgian Blonde, Dubbel, Tripel,
Pale, Strong Golden and Strong Dark Ales, as well as German Doppelbock.
Awards for all categories will be announced following the MOM and Best
Of Show judging. There will be 2 separate categories for BOS:
Beer and Mead/Cider. Rosette ribbons featuring our famous 'Drunk Monk'
will be awarded for 1st, 2nd and 3rd places for each category. Special
ribbons will be awarded for 2nd and 3rd BOS and MOM, and engraved plaques
will be the prizes for 1st BOS and MOM.

Of special note is that the winner of the Beer BOS will have the
opportunity to assist in the scaling up and brewing of their award-winning
recipe at Walter Payton's Roundhouse, of Aurora, IL. Please see rules
for details.

Drunk Monk Challenge entries are $7 for the first entry, and $5 each
additional entry. Menace of the Monastery entries are $5 each.

Entries will be accepted between February 28 and March 7.
There are several drop off locations in the Chicagoland area.

Entries can be shipped to:

The Drunk Monk Challenge,
c/o Walter Payton's Roundhouse - America's Brewing Company,
205 North Broadway, Aurora, IL 60505, ATTN: Mike Rybinski
NO DROP OFFS ALLOWED AT THIS LOCATION!

Full details, rules, entry forms, etc. can be found at the UKG website:
http://www.knaves.org/DMC/index.htm


Good luck and thanks!


Na Zdrowie,
John Kleczewski
2009 DMC organizer
http://www.knaves.org/DMC/index.htm


------------------------------

Date: Fri, 20 Feb 2009 13:20:08 -0500
From: Kai Troester <kai at braukaiser.com>
Subject: Re: Thermal Mass

Matt makes a very good point with the heat of hydration. I didn't know
about this until I read it in Brigg's book myself. Then I also
experienced it when I used a bag of BestMalz Dark Munich which
appeared to be drier than the Weyermann malt that I usually use. And I
notices that the temp after mixing malt and water was always a little
more than what my previous experiences were.

So there is yet another factor that we would need to consider. Even
before knowing about this I had completely abandoned any attempt in
precisely calculating the temp of the stike water. Here are the
options that I currently use as I'm using quite a number of different
mash schedules depending on the beer I'm making:

- single infusion: dough in a little thicker and shoot for a temp
between 155 and 145 then use boiling water infusions to reach the sacc
rest temp. If you like to hold a short protein rest, stay closer to
155 and rest there for 10-20 min.
- decoction: estimate the amout of decoction needed based on this
simple equation: T * (V1 + V2) = T1 * V1 + T2 * V2 and add 10-20%.
Then add the decoction in stages until you hit the rest temp. Add the
remainder a little later when it has cooled to be closer to the rest
temp
- direct heat (stove top) mashing: this has become a recent favorite
of mine as I now like to mash in my brew kettle on the stove top and
then boil on the deck. Dough in below the rest temp and use heat to
reach the rest temp. A 5 gal mash holds it's temp very well when
siting on a styrofoam board and being wrapped in a few blankets.

Kai


------------------------------

Date: Fri, 20 Feb 2009 15:52:08 -0500
From: steve alexander <steve-alexander at roadrunner.com>
Subject: Metric ?

Kevin Elsken says ...
> Subject: Thermal Mass
>
> Bill,
>
> First of all, for goodness sakes man, come over to the dark side and
> just use the metric system! It is just so much better and easier.
>
This is the system that was developed with a 'length' based on a bad
estimate of the distance from equator to pole of some mostly harmless
planet, with 'time' based on the planet's solar day divided by 86400
((according to the Sumerian number system and time units - lost culture
of the same planet)) and with 'mass' determined by H2Oper unit volume at
a given temperature - where temperature is expressed in units based on
the phase change of H2O at some ambient pressure (note the circularity
of defining mass in terms that require defining temps therefore pressure
(pressure is M.L-1.T-2)) ... many of the units are divided by powers
of - and all expressed in a base - determined by the typical number of
flanges on the forepaws of a primate species.

Easier - yes if you count on your fingers and toes. Better -- if I
laugh any harder beer comes out my nose.

-S

------------------------------
End of HOMEBREW Digest #5509, 02/20/09
*************************************
-------

Thursday, February 19, 2009

Homebrew Digest #5508 (February 19, 2009)

HOMEBREW Digest #5508 Thu 19 February 2009


FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
Digest Janitor: pbabcock at hbd.org


***************************************************************
TODAY'S HOME BREW DIGEST BROUGHT TO YOU BY:

Sponsor The Home Brew Digest!
Visit http://www.hbd.org/sponsorhbd.shtml to learn how

Support those who support you! Visit our sponsor's site!
********** Also visit http://hbd.org/hbdsponsors.html *********

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501(c)3 not-for-profit organization under IRS rules (see the
FAQ at http://hbd.org for details of this status). Donations
can be made by check to Home Brew Digest mailed to:

HBD Server Fund
PO Box 871309
Canton Township, MI 48187-6309

or by paypal to address serverfund@hbd.org. DONATIONS of $250
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amount are considered paid advertisement, and may be deductible
under IRS rules as a business expense. Please consult with your
tax professional, then see http://hbd.org for available
sponsorship opportunities.
***************************************************************


Contents:
Re: Heat calculations and thermal mass (Matt)
Lansing Water ("A.J deLange")
Thermal Mass of Mash Tuns ("A.J deLange")
Re: Thermal Mass (Joe Walts)
Re: Heat calculations and thermal mass (Calvin Perilloux)
Boston Homebrew Competition - Call for Judges (Eric Wooten)
Thermal Mass (Kevin Elsken)


* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* The HBD Logo Store is now open! *
* http://www.hbd.org/store.html *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* Beer is our obsession and we're late for therapy! *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *

NOTE: With the economy as it is, the HBD is struggling to
meet its meager operating expenses of approximately $3400
per year. If less than half of those currently directly
subscribed to the HBD sent in a mere $5.00, the HBD would
be able to easily meet its annual expenses, with room to
spare for next year. Please consider it.

As always, donors and donations are publicly acknowledged
and accounted for on the HBD web page. THank you


Send articles for __publication_only__ to post@hbd.org

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instead to http://homebrewfleamarket.com and post a free ad there.

The HBD is a copyrighted document. The compilation is copyright
HBD.ORG. Individual postings are copyright by their authors. ASK
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JANITORs on duty: Pat Babcock (pbabcock at hbd dot org), Jason Henning,
and Spencer Thomas


----------------------------------------------------------------------


Date: Wed, 18 Feb 2009 20:42:02 -0800 (PST)
From: Matt <baumssl27 at yahoo.com>
Subject: Re: Heat calculations and thermal mass

> I am wondering what is the cause of this discrepancy.

Slaking heat! The hydration of malt involves chemical
reactions that release significant amounts of heat. Thus
it *appears* to require less heat than expected to bring
the cold mash tun up to mash temp.

For not very detailed details, take a look at Malting and
Brewing Science by Briggs and Shanks on google books, and
search for "slaking heat." A 5F temp shift is indicated
under pretty standard conditions.

For single infusion mashes at 150F at 1.5 qt/lb in my
system, the two effects cancel well enough that I routinely
ignore them both and hit mash temps to within 1F (and I
don't measure my strike water volume with much care, either).

Unfortunately it's not always so easy. Mash tun thermal
mass and slaking heat have different effects under different
mash conditions and a single "fudge factor" can't account
for both of them at once. More calculation complexity is
needed to account for them well. Further, theoretical values
are not easy to come by and at least for me the numbers in
the above reference don't work well (half works much better).
This is not surprising given the complex nature of the
reaction, different malt grinds, many variables, etc.
I think one would have to be very lucky to arrive at a formula
to predict mash temps to within, say, 1F on a given system
without some fairly thorough observations of different mashes
on that system.

Matt



------------------------------

Date: Thu, 19 Feb 2009 08:08:02 -0500
From: "A.J deLange" <ajdel at cox.net>
Subject: Lansing Water

The water in question has Ca: 20, Mg: 9.7, Na: 44, SO4: 70; Cl: 46,
HCO3 42.1 all assumed to be mg/L which is a reasonable assumption as
those units cause the profile charge imbalance to be only 4% which is
pretty good i.e. the profile is consistent (I assumed pH 7.5 at 20 C).
This water is not very hard (total hardness 89.8 ppm as CaCO3 of which
37 is temporary) nor very alkaline (37 ppm as CaCO3) with a very
modest Residual Alkalinity of 17 ppm as CaCO3 from which an upward pH
shift (relative to distilled water) of only 0.03 is to be expected.
IOW no action should be required to set mash pH with base malts and
even a small amount of colored malt should result in a good value.

The water is well undersaturated with respect to calcium carbonate
i.e. no calcium carbonate would be expected to precipitate upon
standing but somewhat over saturated with respect to CO2 so that gas
can be expected to escape over time with a gradual increase in pH.

It has fair amounts of sulfate and chloride so beers made with it may
have a round, full bodies character and hops will be perceived as
somewhat dry and a bit rough. You couldn't use this water for delicate
continental lagers or similar beers because of the sulfate. There may
be a mineral crispness to beers made with this water and perhaps a
hint of saltiness (does it taste salty from the tap?).

Adding gypsum at the rate of 0.5 gram/liter (12.5 grams in 25 L)
obviously increases the sulfate (to 349 mg/L) and the calcium
hardness (total to 380 while temporary hardness stays the same as the
hardness exceeds the alkalinity) dramatically. The extra calcium
decreases the residual alkalinity to -67 ppm as CaCO3 which predicts a
decrease of mash pH (relative to a distilled water mash) of 0.11 pH.
Because a lot of doubly charged ions (Ca++, SO4--)have been added the
ionic strength changes enough to induce a small pH shift in the water
itself (about 0.02 pH in the acid direction) but the water is still
undersaturated (saturation pH is 7.83) with respect to calcium
carbonate because the alkalinity is so low below 1 mEq/L (50 ppm).
Adding gypsum does not change alkalinity. It, therefore, not likely
that boiling will cause anything to precipitate (as it would in harder
waters with higher alkalinity). Boiling, as a rule of thumb, reduces
hard, carbonate water alkalinity down to about 1 mEq/L (50 ppm as
CaCO3) and this water is below that (even post treatment).

All the information extracted from the basic water report presented
here came from my water analysis spreadsheet which is at
http:/www.wetnewf.org/Brewing_articles/BURP_OCT08
IOW, you can get all this info yourself if you are so inclined though
expect to spend some time trying to figure the thing out. There are
extensive instructions but I know this is complex stuff (based on how
many years it has taken me to get this far).

A. J.


------------------------------

Date: Thu, 19 Feb 2009 09:17:20 -0500
From: "A.J deLange" <ajdel at cox.net>
Subject: Thermal Mass of Mash Tuns

It's been a while since we did the algorithms for ProMash so I'd have
to go back and look at some notes but as I recall the big problem with
pouring hot water into a tun at room temperature is that the water
loses so much heat in the transfer that it throws the calculation off.
Thinking it over it seems a better way might be to fill the tun with a
known mass of water at room temperature, heat the water to a few
degrees above room temperature, let it equilibrate (stand for an hour
or so with occasional stirring) or put some hot water in the tun and
let it stand, with stirring, until its temperature is a few degrees
above room temperature and then add a known mass of water at room
temperature. This prevents heat loss from either the water in the tun
(even if it's a few degrees above ambient some heat will be lost but
the rate of loss is proportional to the temperature difference) or the
water added. Note that I say known "mass" of water. Probably the best
way to do this would be to put the tun on a scale. When its empty you
have its weight (not that you really need that) but you can tare it to
measure the mass of warm water and then take the difference after you
add the cooler water. I'm talking mass here because the volume of a
given mass of water does change appreciably with temperature (several
percent). Another thing to be aware of is that the heat capacity of
water does change somewhat as a function of temperature. I handled
this relatively simply by computing an average over any given
temperature range i.e. if you go from T0 to T1<T0 when you add cold
water the average heat capacity is simply (1/(T0-
T1))*Integral_from_T1_to_T0[Cp(T) dT)]. You can find Cp(T) in
handbooks, Wikipedia etc. Errors induced by ignoring this will be much
smaller than errors induced by ignoring density changes and being
unable to control heat losses.

A.J.


------------------------------

Date: Thu, 19 Feb 2009 08:33:03 -0600
From: Joe Walts <jwalts at gmail.com>
Subject: Re: Thermal Mass

Hey Bill, just a couple of quick and dirty guesses here:

First off, you're not raising the temperature of your entire mash tun to the
desired mash temperature. Instead, you're creating a gradient through the
vessel walls where the inside surfaces are at the mash temperature and the
outside surfaces are at ambient temperature. The latter scenario requires
less heat energy from the strike water, Unless you model the gradient in
your heat capacity calculation, your experiment will result in a lower
thermal mass.

The second complication is the time. How long does it take the system
become stable, i.e. to where you're slowly losing heat to the atmosphere
instead of to the vessel itself? I have no idea, so I just overheat my
strike water by 10 degrees, dump it in the mash tun and wait to add the
grain until the water cools to my desired strike temperature (which doesn't
include the thermal mass of the mash tun in its calculation).

Joe


------------------------------

Date: Thu, 19 Feb 2009 06:56:39 -0800 (PST)
From: Calvin Perilloux <calvinperilloux at yahoo.com>
Subject: Re: Heat calculations and thermal mass

Regarding Bill Pierce's formulas for thermal mash...
That's good research for an English major, Bill! ;-)

> 0.119*32.92 = 3.92
> Unfortunately this is in conflict with the value
> I arrived at (1.918 lbs.) based on my formula and
> experiment with hot water as described above.

You are now into the scientific area best explained by this quote:

"Well, that's great in practice, but does it work in theory?"

Without delving too much into the formulas, and not having my
trusty CRC handbook nearby anyway, I'll highlight a few things
to consider, not only for your setup but for others:

The structure of your vessel can have some significant effect.
In the case of a converted keg, the heavy rings top and bottom
are to some extent isolated from the rest of the body. Sure,
it's thermally attached as one piece of stainless, but my guess
is that the conduction might not be great enough to rapidly
heat those. That would leave the body of the keg absorbing
most of the heat and not the edges.

So in your empirical tests it could show a lower thermal heat
because those outer areas are not being heated (as much).

In other cases, such as people using stainless pots for mash
tuns, the handles are a minimal factor (as above), but keep
in mind that there is often an aluminum layer in the base
(for heat distribution because stainless is such a poor heat
conductor), and this might make it hard to get the results
just right on paper -- do you know how much the alu-sandwich
inside there weighs?

There is also the heat loss that you encounter in bringing
the hot water to the mash tun and pouring it. I find that
this is not that large but definitely not insignificant.

In my own opinion, the very best way to do this is to just
do the empirical work on your own system and use that number.
When you do that, the heat loss, mixed-metal proportion, and
structural features will all be accounted for in your end result.

Calvin Perilloux
Middletown, Maryland, USA

------------------------------

Date: Thu, 19 Feb 2009 10:19:58 -0500
From: Eric Wooten <ecwooten at gmail.com>
Subject: Boston Homebrew Competition - Call for Judges

The 14th Boston Homebrew Competition is coming up on Saturday, February
28th. It will be held at the law offices of Holland and Knight, located in
the Back Bay region of Boston about 2 blocks from the Public Garden (Back
Bay and Arlington Stations are within easy walking distance for those
traveling by MBTA). Preliminary counts yield a total of 271 entries this
year (the entry window is now closed). We are still looking for both
experienced and novice judges and stewards to help with this years
competition.

If you are able to help with judging or stewarding, please fill out the
judge registration form at http://bhc.wort.org/judgereg.shtml.
Further details about the judging process can be found at:
http://bhc.wort.org/judgeinfo.shtml. Although the competition site is easily
accessible by the T and Commuter Rail, on site parking is available and the
competition will cover parking fees for all individuals who register in
advance.

Important Note: As the competition will be held in a secured building,
pre-registration to judge or steward is required. Building security needs a
list of people to provide to their check-in desk in advance of the
competition.

If you have already signed up to help out: thanks in advance for helping us
put on another great competition; Mark Irwin, the judging coordinator for
BHC 14, will be contacting you soon with the final details. If any of you
have any questions please do not hesitate to contact us.

Eric Wooten, Competition Organizer (organizer at wort.org)
Mark Irwin, Judging Coordinator (irwin at wort.org)
Wade Hicks, Entry Organizer (treasurer at wort.org)


------------------------------

Date: Thu, 19 Feb 2009 21:17:27 -0500
From: Kevin Elsken <littleboybrew at verizon.net>
Subject: Thermal Mass

Bill,

First of all, for goodness sakes man, come over to the dark side and
just use the metric system! It is just so much better and easier.

Anyway, I have gone through many turns trying to hammer out thermal mass
values to give consistent mash temperatures. I suspect won't be the
first to mention that your calculation implies your entire mash tun was
heated from 70 def F to 157 deg F. In truth, only a portion of the 32
lb+ tun is actually increasing in temperature from 70 to 157. The
converted kegs have heavy rolled rings around the top and bottom that
most certainly did not change temperature that much. According to the
quick calculations I made, the water lost about 176 kJ, but it would
require almost 361 kJ to raise your mash tun from 70 to 157 F.

Incidentally, insulated coolers are primarily polyurethane foam, which
has a heat capacity of about 1.5 kJ/kg. The trick to the calculation
with an insulated cooler is that due to the excellent insulation value
of the cooler, the outside remains at ambient temperature, so the actual
temperature rise is only about one half the difference between the
inside and outside of the cooler.

Kevin Elsken
Little Boy Brewery
Upper Saint Clair, PA


------------------------------
End of HOMEBREW Digest #5508, 02/19/09
*************************************
-------

Wednesday, February 18, 2009

Homebrew Digest #5507 (February 18, 2009)

HOMEBREW Digest #5507 Wed 18 February 2009


FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
Digest Janitor: pbabcock at hbd.org


***************************************************************
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***************************************************************


Contents:
Re: Helium ("Craig S. Cottingham")
Re: Helium (beerdan)
RE: Helium (Josh Knarr)
Water Questions (Jim Stansell)
Heat calculations and thermal mass (caution: geek alert) ("Bill Pierce")


* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
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* * * * * * * * * * * * * * * * * * * * * * * * * * * * *

NOTE: With the economy as it is, the HBD is struggling to
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JANITORs on duty: Pat Babcock (pbabcock at hbd dot org), Jason Henning,
and Spencer Thomas


----------------------------------------------------------------------


Date: Tue, 17 Feb 2009 23:21:26 -0600
From: "Craig S. Cottingham" <craig.cottingham at gmail.com>
Subject: Re: Helium

On Feb 17, 2009, at 14:35, "Chad Stevens" <zuvaruvi at cox.net> wrote:

> Got my CO2 tank filled yesterday. On the way out of the shop I saw
> a helium
> tank. Brewers being mad scientists by default, I thought to myself,
> "wouldn't that be an interesting party trick, Helium 'carbonated'
> beer."
> Take a sip, then sing, "We represent, the lollipop guild...."


Interesting idea, but it wouldn't work. The solubility of helium in
water is one one-thousandth that of carbon dioxide at beer
temperatures. Nitrogen is ten times more soluble than helium, so
imagine a Guinness stout tap, but a lot less so.

- --
Craig S. Cottingham
BJCP Certified judge from Olathe, KS ([621, 251.1deg] Apparent
Rennerian)
craig.cottingham at gmail.com
+1 (913) 826-6896 or Skype me at CraigCottingham

------------------------------

Date: Wed, 18 Feb 2009 08:22:54 -0500
From: beerdan at optonline.net
Subject: Re: Helium

You'll find there are several problems with this. First is the cost. Helium is
expensive compared to other gases as it is not abundant in our atmosphere.
Also, I don't have the numbers in front of me but helium does not easily
diffuse in liquids unless the pressure is very high or the temperature is very
cold, or both. Instead of about 10 psi for CO2, you may have to triple or
quadruple it for helium to achieve a similar level of 'carbonation' or
heliumnation' as the case may be. And then, when you released the
pressure when dispensing, it would immediately come out of solution,
leaving a flat beer behind.

I would be curious to see what a head of helium foam would look like.
Helium being the second smallest atom.. would the bubbles be microspoic
and produce a thick, small head or blow right through and leave nothing
behind?

Not a very techie answer but my experience comes from scuba diving and
the use of enriched air nitrox and trimix (oxygen, nitrogen, helium mix)
gases and the effects of them when under pressure in the blood stream.

> ------------------------------
>
> Date: Tue, 17 Feb 2009 14:35:49 -0800
> From: "Chad Stevens" <zuvaruvi at cox.net>
> Subject: Helium
>
> Got my CO2 tank filled yesterday. On the way out of the shop I saw a helium
> tank. Brewers being mad scientists by default, I thought to myself,
> "wouldn't that be an interesting party trick, Helium 'carbonated' beer."
> Take a sip, then sing, "We represent, the lollipop guild...."
>
> Anyone tried it?
>
> Chad Stevens
> QUAFF
> San Diego
> www.sdfair.com/beer

------------------------------

Date: Wed, 18 Feb 2009 08:57:30 -0500
From: Josh Knarr <josh.knarr at gmail.com>
Subject: RE: Helium

The helium works by going into your lungs so your vocal chords vibrate
much more quickly.

It wouldn't be funny until someone burped, but then it wouldn't be
funny anyway because the beer would taste weird. Helium is colorless
and odorless, and probably tasteless as well. Unless you made a beer
which didn't want to be heavily carbonated, helium probably wouldn't
fly. (pun intended). I would think there's a serious risk of the beer
going flat.

- --

George Burns - "I would go out with women my age, but there are no
women my age."


------------------------------

Date: Wed, 18 Feb 2009 15:16:00 -0500
From: Jim Stansell <jim.stansell at comcast.net>
Subject: Water Questions

In the book "Brew Classic European Beers" at home, Wheeler and Protz
comment that their typical water treatment is to add 12g of calcium
sulfate (CaSO4) to about 25 liters of boiling water water, and then
let the precipitate settle out before racking the water off and
leaving the scale behind. Exactly what is being left behind?
Temporary hardness? Permanent hardness?

Here's my water profile (Lansing, Michigan area) in ppm:
Calcium: (Ca) 20
Magnesium (Mg): 9.7
Sodium (Na): 44
Sulfate (SO4): 70
Chloride (Cl): 46
Bicarbonate (HCO3): 42.1

(1) What comments does anyone have about this water?

(2) What would boiling it with CaSO4 accomplish?

------------------------------

Date: Wed, 18 Feb 2009 21:56:11 -0500
From: "Bill Pierce" <BillPierce at aol.com>
Subject: Heat calculations and thermal mass (caution: geek alert)

Sometimes I get so geeky I scare myself. That's the conclusion as I
continue to revise my brewing spreadsheet, a 10-year work in
progress. My graduate degree was in English, so it's sometimes a
stretch to come to terms with all the math involved.

Lately, I've been looking at the various formulas involving
temperature in mashing, and preparing an article about the subject.
Most of the formulas include a variable called "thermal mass," which
as it relates to brewing is the resistance to changes in
temperature, thereby requiring additional heat to effect a
temperature change. As most all-grain brewers know, the mash tun
temperature is one of the reasons, along with the temperature of the
grain, why the strike water must be quite a bit hotter than the
desired initial mash temperature.

Many homebrewers are acquainted with the thermal mass value from
ProMash. The Help file mentions that it can be set to a
predetermined value between 0 and 1.0, and suggests a value of 0 if
you preheat the mash tun. If not, it suggests initially setting the
value to 0.3 and later adjusting it according to the accuracy of the
results. I could not find any specific formula for calculating the
thermal mass in
this way. The problem is that ProMash is somewhat misleading in its
use of this term. "Thermal mass" implies a weight measured in pounds
or kilograms rather than a kind of "fudge factor" in the
calculations. Indeed if we examine what thermal mass really means,
we discover that the weight of the vessel is involved.

After a lot of working with the math, eventually I derived a more
accurate formula for the temperature of the strike water to achieve
a desired mash temperature:

Ts =
((Td*(ThM+(2.08635*Vw)+(0.4*Wg)))-(Tg*0.4*Wg))-(Tm*ThM))/(2.08635*Wv
)

Where:
Ts = Temperature of strike water to achieve a desired mash
temperature (degrees F)
Td = Desired mash temperature after addition of grain and strike
water (degrees F)
ThM = Thermal mass of mash tun (pounds)
Vw = Volume of strike water (quarts)
Wg = Weight of grain (pounds)
Tg = Temperature of grain (degrees F)
Tm = Temperature of mash tun (degrees F--unless it is preheated,
this is the ambient air temperature)

The 0.4 coefficients are the published heat capacity of malt (with a
moisture content of 4 percent); by convention the heat capacity of
water is 1.0. The 2.08635 coefficients are the weight in pounds of 1
quart of water. Metric brewers can substitute degrees C for degrees
F and kilograms for pounds without changing the formula. As for the
water volume, if you are using liters, omit the 2.08635 coefficient.
Conveniently, the metric system is based on 1 liter of water
weighing 1 kilogram.

The benefit of this formula over others is that it takes into
account both the thermal mass of the mash tun and the mash tun
temperature. A deficiency of some brewing software is that the
strike water temperature calculations can be in error if the mash
tun is very cold, for example, in the winter. Accounting for the
temperature of the mash tun resolves this issue.

The formula raises the question of what is the mash tun thermal mass
value. Apart from some suggestions in the ProMash Help file and
elsewhere, there is very little published about this subject.
However,
it is possible to determine the mash tun thermal mass value
empirically. By rearranging the terms, if the other values are
known, the equation above can be solved for the vessel's thermal
mass (I omitted the grain values because I wanted to experiment with
water only). It becomes:

ThM = ((Ts-Td)*2.08635*Vw)/(Td-Tm)

The result will be the vessel's thermal mass in pounds or kilograms.
Metric brewers can directly substitute the temperature values in
degrees C, the weight in kilograms and the volume in liters,
omitting the 2.08635 coefficient for the water volume conversion to
mass in pounds.

To use the formula, measure the temperature of the empty vessel
(Tm). Normally this is the same as the ambient air temperature.
Heat the volume of strike water (Vw) for a typical batch at a
typical strike
water temperature (Ts). Add the hot water to the vessel. Cover, wait
a few minutes and measure the water temperature (Td). Use the
formula to calculate the vessel's thermal mass (ThM). Once again,
metric brewers can use their units and omit the 2.08635 coefficient
that converts the water volume in quarts to mass in pounds.

Using this formula, I did an experiment with hot water and my own
converted keg mash tun. Using 16 quarts of water at 162 F and an
ambient air temperature of 70 F, it resulted in a final temperature
of 157 F and a thermal mass value of 1.918 lbs.

Beyond empirical measurement, the thermal mass can be calculated
based on the thermal properties of a vessel's material. While I
wouldn't care to hazard a guess about the composition of plastic
coolers (the outer shell and inner insulation), stainless steel has
measured heat properties. If you mash in a converted keg or pot made
of 304 stainless, there is published data for the specific heat,
that is, the
amount of energy in joules per gram (or kilojoules per kilogram)
necessary to raise the temperature 1 degree Kelvin (or Celsius).
This value is 0.50 kJ/kg. If we convert this value to that which is
relative to water (specific heat 4.19 kJ/kg), we can ignore the
measuring system (metric or American/British). Therefore the heat
capacity of 304 stainless relative to water is 0.5/4.19 = 0.119.
This is true for temperatures measured in both degrees Celsius and
Fahrenheit.

The thermal mass depends on the mass (weight) of the vessel as well
as the heat capacity. It is necessary to weigh the vessel in order
to calculate the thermal mass. Using the heat capacity of 304
stainless to calculate the thermal mass of my own converted keg mash
tun, and multiplying by the measured weight of 32.92 lbs., I arrived
at a value of 3.92 lbs:

0.119*32.92 = 3.92

Unfortunately this is in conflict with the value I arrived at (1.918
lbs.) based on my formula and experiment with hot water as described
above. I am wondering what is the cause of this discrepancy. In the
interest of brewing science, perhaps someone who is as geeky as I am
could shed some light on this. I will give credit for the assistance
when I publish my article.

Brew on!

Bill Pierce
Cellar Door Homebrewery
Burlington, Ontario

------------------------------
End of HOMEBREW Digest #5507, 02/18/09
*************************************
-------

Tuesday, February 17, 2009

Homebrew Digest #5506 (February 17, 2009)

HOMEBREW Digest #5506 Tue 17 February 2009


FORUM ON BEER, HOMEBREWING, AND RELATED ISSUES
Digest Janitor: pbabcock at hbd.org


***************************************************************
TODAY'S HOME BREW DIGEST BROUGHT TO YOU BY:

Sponsor The Home Brew Digest!
Visit http://www.hbd.org/sponsorhbd.shtml to learn how

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501(c)3 not-for-profit organization under IRS rules (see the
FAQ at http://hbd.org for details of this status). Donations
can be made by check to Home Brew Digest mailed to:

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or by paypal to address serverfund@hbd.org. DONATIONS of $250
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amount are considered paid advertisement, and may be deductible
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tax professional, then see http://hbd.org for available
sponsorship opportunities.
***************************************************************


Contents:
yeast propgation (Rob Schlank)
Re: Should I repitch? (Stephen Jorgensen)
Should I repitch? (Scott Birdwell)
Helium ("Chad Stevens")
more yeast perf ... pt 1 ("Steve.Alexander")
more yeast perf ... pt 2 ("Steve.Alexander")
Kalamazoo Stout (Tim Eitniear)
2009 South Shore Brewoff - competition announcement ("jeff_ri")


* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* The HBD Logo Store is now open! *
* http://www.hbd.org/store.html *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *
* Beer is our obsession and we're late for therapy! *
* * * * * * * * * * * * * * * * * * * * * * * * * * * * *

NOTE: With the economy as it is, the HBD is struggling to
meet its meager operating expenses of approximately $3400
per year. If less than half of those currently directly
subscribed to the HBD sent in a mere $5.00, the HBD would
be able to easily meet its annual expenses, with room to
spare for next year. Please consider it.

As always, donors and donations are publicly acknowledged
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cannot be reproduced by any means for sale or profit.

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JANITORs on duty: Pat Babcock (pbabcock at hbd dot org), Jason Henning,
and Spencer Thomas


----------------------------------------------------------------------


Date: Tue, 17 Feb 2009 09:11:56 -0500
From: Rob Schlank <rschlank at comcast.net>
Subject: yeast propgation

Joshua WIlkins wrote, "The smack packs that Wyeast uses
contains nutrients and the sachet that you pop on the inside is the yeast
cells."

Not to nitpick, but this is incorrect. The sachet contains the nutrients,
not the cells. You can, if you wish, pitch the cells into a starter without
'smacking' the sachet. This is per Dave Logsdon at Wyeast in an interview, I
believe from an old TBN show. I have done this myslef several times, though
now I smack the pack just to get the nutrients into the starter as well.

- --
Rob Schlank


------------------------------

Date: Tue, 17 Feb 2009 09:35:17 -0600
From: Stephen Jorgensen <stephen at ultraemail.net>
Subject: Re: Should I repitch?

"I have an IPA in the secondary for about 10 weeks. It looks clear and tastes
decent upon sampling."


In my experience there is no more disappointing result in home brewing
than a bottle of sweet, flat beer. Yes you should use fresh yeast to
package your IPA but an entire envelope is not necessary.

I don't have the correct cells / ml numbers to hand but I am sure there
are multitudes of brewers reading HBD that know them by heart. I
generally use about 1/10 the amount for bottling as I did when pitching
the wort. In the case of Danstar Nottingham (no affiliation) which is
my bottling yeast of choice I use 2-3 g for a 6 gallon batch. For an
IPA I would go with 3.


------------------------------

Date: Tue, 17 Feb 2009 13:37:03 -0600
From: Scott Birdwell <defalcos at sbcglobal.net>
Subject: Should I repitch?

Regarding Tom Puskar's question, "Should I repitch. . ."

"For a number of reasons ranging from illness, work and family issues,
I have
an IPA in the secondary for about 10 weeks. It looks clear and tastes
decent upon sampling.

I'm hoping to bottle it (FINALLY) this coming week and wondered if I
should
add some additional yeast for carbonation. I keep a few envelopes of
dry
yeast around and could proof one up and add it to the bottling
bucket. I
haven't checked the gravity in a few weeks but last check it was around
1.015 and hadn't changed for a while."

Tom,
It's like chicken soup. . . it couldn't hurt! Just rehydrate the
dried yeast in some lukewarm water and mix it thoroughly into the beer
just before/after you mix in your priming sugar. You should have
carbonated beer within a couple of weeks. Good luck!

Scott Birdwell
DeFalco's Home Wine & Beer Supplies
Houston TX


------------------------------

Date: Tue, 17 Feb 2009 14:35:49 -0800
From: "Chad Stevens" <zuvaruvi at cox.net>
Subject: Helium

Got my CO2 tank filled yesterday. On the way out of the shop I saw a helium
tank. Brewers being mad scientists by default, I thought to myself,
"wouldn't that be an interesting party trick, Helium 'carbonated' beer."
Take a sip, then sing, "We represent, the lollipop guild...."

Anyone tried it?

Chad Stevens
QUAFF
San Diego
www.sdfair.com/beer

------------------------------

Date: Tue, 17 Feb 2009 18:03:56 -0500
From: "Steve.Alexander" <steve-alexander at roadrunner.com>
Subject: more yeast perf ... pt 1

Uhoh - 8k bouncy bouncy

I've used imprecise language and now several ppl have posted their own
(sometimes odd) views on terminology and we are making a mish-mash of
this discussion. In common use "ferment" merely means microbiological
activity. I didn't really think we need/want to delve so deeply on this
one but ....

According to Brock's "Biology of Microorganisms", a very widely used and
highly regarded text we have ... "Fermentation - Catabolic reactions
producing ATP in which organic compounds serve as both primary electron
donors and ultimate electron acceptors and ATP is produced by
substrate-level phosphorylation". And, "Respiration - Catabolic
reactions producing ATP, in which either organic or inorganic compounds
are primary electron donors and organic or inorganic compounds are
ultimate electron acceptors". If you study the definitions carefully
you will see that respiration is any ATP energy pathway, while
fermentation additionally requires organic donors, organic acceptors and
substrate-level phosphorylation (as opposed to oxidative phosphorylation
pathway). Brock divides catabolic pathways into "aerobic respiration"
and "anaerobic respiration", and OBVIOUSLY he's not referring to the
environment but the metabolism.

According to Brock's ... Fermentation IS a type of respiration !!!!
Aerobic/Anaerobic can and usually does refer to the metabolism NOT the
environment.
. so perhaps we all get a big fat F- for terminology.

Nester-Robert-Nester "Microbiology", and Stryker "Biochemistry" says
that respiration requires any inorganic electron acceptor.
Mathews-vanHolde*, *"Biochemistry", says respiration requires oxygen as
the electron acceptor.

===========
The two concepts we are trying to distinguish here are related to how
the metabolic phosphorylation of ADP to ATP occurs, but thats awfully
deep into the nuts & bolts.

In conventional brewery fermentation with Saccharomyces yeast (of
course) none of the catabolic(energy producing) pathways use free
oxygen. Brewery yeast induce sugar or create these from enzymatic
breakdown of sugar polymers.

First, each hexose sugar is converted to two pyruvates + 2 H2O + energy
as a net +2 ATP. This is known as the Embden-Meyerhof-Parnas (EMP)
pathway and is one of several glycolytic pathways. The ATP is produced
by substrate-level conversions of bisphosphoglycerate and
phosphoenolpyruvate.

The pyruvate can readily, enzymatically be converted to lactate (as in
your muscles) acetate+formate or acetaldehyde+CO2. In yeast the
pyruvate is converted to acetaldehyde+CO2 and the acetaldehyde is
reduced (the organic electron acceptor) into ethanol.

The EMP pathway also converts 2 NAD+ to 2 NADH and this is a great
energy store (1 NADH can be converted to 3 ATP with some oxygen) BUT to
accomplish the redox balance all of the NADH must be used to reduce
acetaldehyde to ethanol. In anaerobic condition it is always necessary
to use the NADH of glycolysis to reduce the pyruvate product.

No oxygen is required for this catabolic pathway, and the net energy
yield is only 2 ATP per hexose.

- --
Under ABNORMAL conditions we can get brewing yeast to use another
catabolic pathway using sugars. The yeast induce sugars as before. The
EMP glycolytic pathway occurs too producing pyruvate and ATP as before.
The next pathway is the "Citric Acid Cycle"(CAC) , aka Tri-Carboxylic
Acid Cycle(TCA) and more formally as the Szent-Gyorgyi/Krebs cycle (note
Szent-Gyorgyi is one guy). The major plot is that the 3-carbon chain
pyruvate is converted to 3 CO2 molecules by repeated decarboxylation.
First the pyruvate is converted to AcetylCoA+CO2, then the Acetyl-CoA
plus an oxalacetate(from...see below) becomes ketoglutate+CO2, then
the ketoglutarate becomes succinyl-CoA+CO2 and finally the succinyl is
reverted to oxalacetate and added back at the start of the next cycle.

The CAC+Glycolysis results in net yield 38ATP of energy per hexose and
only 4 of the ATPs of the total produced are by substrate-level
phosphorylation, the rest by oxidative phosphorylation.
========

Heading out of the chem lab and back toward the brewery .....

There are some silly notions perpetrated and/or perpetuation by poorly
researched HB books. Brewery yeast under normal brewing conditions
NEVER use the CAC cycle (almost never). Not even when they are pitched
into well oxygenated normal wort. Now IF you use an open fermenter then
after all the sugars are used up the yeast can oxidize ethanol back into
aldehyde then convert to acetyl-CoA which can then enter the CAC cycle
and yields a lots of energy. The "back up the tree" process can also
throw off some lactate and acetate. It's unclear how rapidly this path
can operate but distilleries use open fermentation and I've seen figures
indicating that a few percent of the ethanol is used per 24 hours of
extra delay. I would imagine that oxygen is a limiting factor in those
conditions.

If you can grow yeast with their metabolism using the CAC cycle, then
there are some metabolic and environmental differences. The yeast are
constantly exposed to free oxygen (needed for the oxidative
phosphorylation) and so they don't accumulate squalene (a precursor to
sterol) but instead they contain a high level of sterol. Similarly
with ever present oxygen yeast can construct (mostly mono-) unsaturated
fats and so these yeast have the best cell membranes around. As the
yeast hit a growth limitation then I would expect that they will store
"storage carbohydrates" abnormally; glycogen accumulates in response to
growth limitations, but also degrades in the presence of oxygen.
Trehalose accumulates in response to a wide array of stresses including
nutrient deficit. So pitching yeast that have finished in aerobic
metabolism is probably nearly ideal except for glycogen, and that's
probably not terribly important unless you plan to store the yeast (then
an anaerobic final finish w/ a little sugar added might be best); and
since these are high in UFA&Sterol so there is less need to aerate the wort.

Yeast in anaerobic conditions suppress the enzymes of the CAC cycles,
and in aerobic conditions they suppress the creation of cytochomes that
are involved in the electron transport for redox balance (far less is
needed). This is NOT a big deal unless you are the sort who gets
ants-in-the-pants if a fermenter isn't bubbling in 20 minutes.

- --
(continued)


------------------------------

Date: Tue, 17 Feb 2009 18:04:25 -0500
From: "Steve.Alexander" <steve-alexander at roadrunner.com>
Subject: more yeast perf ... pt 2

(continued)

Kai T suggests ....


>> > > It might be that low gravity propagation isn't
>> > > good either b/c the yeast may get uses to the lower alcohol/sugar
>> > > concentration both of which are stress factors.
>>
No. High gravity is just a ion pump stressor (yeast must expend more
energy moving ions across cell membranes) and there is no way to
accumulate a tolerance to the added workload except to include more
sterol & UFA per cell to reduce "leakage". It's always best to
propagate yeast at 5-7P.

Joshua Wilkins mentions his experience with a commercial propagator but
.. this doesn't exactly hit the mark either. This sort of propagation
is aimed at providing oxygen to yeast culture, such as a scintered stone
would, but it is not aimed or creating conditions for aerobic metabolism
(the CAC cycle). There is nothing very expensive about scaling this
down to HB level.

His other comments fall solidly into the "old brewers tales" category.
That yeast develop resistance to ethanol and hops doesn't match anything
I've ever read anywhere - and the fact is that all fermentation produces
intracellular ethanol. The "resistance" or more correctly high
tolerance of high level is of extracellular ethanol is from several
studies only related to cell membrane quality and the absence of the
environmental stressors like excess CO2 in solution and the presence of
several specific amino acids which reduce the osmotic stress effect.
When repitching into a barleywine you can and should use sterol&UFA rich
yeast propagated at ~5P.

The idea that you should walk yeast through the sugars they consume (the
order glucose,fructose, maltose, maltotriose is common) before you plop
them into fresh wort has absolutely no advantage. The presence of
glucose inhibits the transport of the maltose & maltotriose ; maltose
inhibits the maltotriose and so on ... and the enzymes for transport
and hydrolysis simple don't last long enough to make any difference at
all. There may be a slight advantage in propagating yeast on glucose
since it's the first sugar they'll get at pitching, , but frankly it's
pretty far down the "don't care" list. So long as the yeast is
reproducing correctly and has the necessary nutrients, then they carry
all the genetic machinery to produce (and alternatively inhibit) the
right enzymes for their *current* conditions and it only takes minutes
for them to make a transition if healthy.

*IF* (this is a huge if) you could force yeast into using the CAC cycle
they would produce roughly 10X the biomass per unit sugar so wort would
be too deficient in nutrients to be useful. Adding nitrogen can
alleviate the nitrogen deficit *BUT* I've recently read that (low)
nitrogen plays a huge role in keeping yeast in aerobic-respiration
metabolism. If nitrogen is low then respiration is preferred (low
nitrogen limits sugar transport), but the low nitrogen also inhibits
growth rate. So you really need to carefully feed both sugar and
nitrogen. Boulton & Quain "Brewing Yeast and Fermentation", suggest
that the only way to get yeast to respire is to slowly feed sugar in a
very low nitrogen environment or to use a chemostats under carbon
(sugar) limitation. A chemostat is a bit of lab gear that allows one to
adjust the input rates into fermenter (with corresponding output) so
that the vessel contains a stable culture. It's not useful for biomass
creation. There are about 3 dozen well know required yeast nutrients
aside from nitrogen and a carbon source(sugar ...) and these won't come
cheap. Urea and a good yeast nutrient are a start but what exactly
provides biotin and pantothenic acid and enzyme cofactors and in what
proportion ?

The only other CAC approach that makes sense is to use a substrate than
cannot undergo glycolysis - so feed your yeast pyruvate or lactate or
ethanol, xylitol or certain glycosides and let then run it thru the CAC
cycle. These are some so called "oxidative substrates", but the trouble
is that aside from pyruvate, which yeast can use which substrate is hit
or miss (The UK NCYC has very incomplete tables for their yeasts).
Then we have the question of how fast can yeast really use oxidative
substrates. This may make this approach even more impractical; I
believe that most can use ethanol, but the rate may be too slow to
provide a decent propagation method.

Trying to grow yeast with CAC metabolism is an interesting hack, but
ultimately costly and difficult. I might feel differently if sugar was
vastly expensive or else if pyruvate and other nutrients very cheap; but
just the opposite is true. It may have a place in producing yeast for
freeze-dried storage, but that's a special application I don't need to
practice. If you learn to do this cheaply and effectively please drop a
note, b/c it would be a great propagation technique.

The only really practical approach I see here is that if you bump oxygen
into a conventional wort starter (say on a stir plate or with a stone)
then your yeast will still be well supplied with UFA and sterols and
you'll have the happy co-incidence that wort has about the right mix of
sugar and nutrients to grow yeast using glycolysis only.

As a very relevant aside, Boulton pioneered the "yeast oxygenator"
method used commercially as Bass Brewers Limited. They take a yeast
slurry, presumably from a finished batch, and add just a bit of 3P wort,
then the add continuous oxygen over a period of several hours. They
continuously measure the yeast oxygen uptake rate. In about 3 hours
the oxygen uptake rate peaks then it drops to a low figure after another
3-4 hours. At that point the yeast have degraded their glycogen store
and produced all the sterol possible. This is pitched directly into
UNoxygenated wort in fermenter. They give figures showing the beer
attenuation rate is superior and far more consistent than wort
oxygenation. Also the there is no significant difference in esters or
other flavor active yeast by-products.

Yeah - by all means get a lot of oxygen into the starter, and less into
the wort ! But there isn't any practical gain to pushing the metabolism
to oxidative phosphorylation on the HB scale.

-S


------------------------------

Date: Tue, 17 Feb 2009 20:17:10 -0600
From: Tim Eitniear <timeitniear at sbcglobal.net>
Subject: Kalamazoo Stout

Hi,
Trying to clone this lovely beer. Found something in the archives from
2002 and I have the zymurgy articles from 2003. Any one have any
suggestions or have found a AG solution to this beer?

Tim
- --
http://nottawaseppibrewing.wordpress.com
A guy walks into a pub with a lump of asphalt on His shoulder, He says to
the bar man give me a pint and one for the road.


------------------------------

Date: Tue, 17 Feb 2009 22:10:38 -0500
From: "jeff_ri" <jeff_ri at cox.net>
Subject: 2009 South Shore Brewoff - competition announcement

The 2009 South Shore Brewoff is the 14th annual homebrew competition
organized by the South Shore Brew Club. The competition is organized to
provide entrants with a high level of evaluation and valuable feedback on
their brewing efforts. Whether you are a novice or a seasoned brewer, we
welcome your participation.

The competition will be held in Mansfield, MA on April 18th, 2009. The
entry deadline is April 3rd, 2009.

All entry information is on the club webpage at:
http://www.southshorebrewclub.org/

Geoffrey McNally (judge coordinator)
Kevin Farrell (competition organizer)


------------------------------
End of HOMEBREW Digest #5506, 02/17/09
*************************************
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