Re: [Biofuel] (was Glycerine Settling Time) removing salt/dirt fromwvo

2007-08-13 Thread Jan Warnqvist
Hello Roderick. A definiyion is on its place:
A salt is basically a compound built up from the reaction of a metal and an 
acid.There are other salts too, but we can leave them for now.  This means that 
soaps are salts, since they are built up from metal ions (Na+ or K+ in 
connection with biodiesel) and fatty acids. These are formed as a by-reaction 
in the trans-esterification process, often encouraged by the water content. 
Salt in every-day talk is NaCl sodium chloride , where in this case the 
chlorine is fetched from HCl, hydrochloric acid. Does this spread any light to 
you ?
You are using acetic acid to break the emulsion. This will create the salts 
potassium or sodium acetate and water. 
Best regards
Jan
  - Original Message - 
  From: Roderick Roth 
  To: biofuel@sustainablelists.org 
  Sent: Sunday, August 12, 2007 6:03 PM
  Subject: Re: [Biofuel] (was Glycerine Settling Time) removing salt/dirt 
fromwvo


   Hello Jan
  May I jump into the discussion? Jan you have just mentioned the word salts 
isn't that one of the ingrediants for making very good quality soap? Hence 
possibly helping make a great emultion during the first wash on the quality 
esters. I am assuming that salts will remain in the whole process, not being 
disolved in any manner from the methoxide right? Some salt should be drained 
with the glycern right? Possibly leaving some salt in the unwashed ester.
My last two reactions have had the same feedstock, ( a very popular 
restaurant which salts their fry's heavily, lol) both reactions were two stage 
acid/base reactions becos the titration is consistantly over 14 eww . 
Here are the wash results from both batches of Quality Tested BD:  
   Reaction #21  using 1500L unwashed oil as a feedstock:the resulting 1380 
Litre batch of quality BD required 3.5 litres of pure 99% vinagar to break the 
first wash emultion. 
   Reaction #22 using  1500L PREWASHED oil of the same feedstock : the 
resulting 1450L batch only required 1 Litre of 99% pure vinagar, to break the 
first wash emultion.  
  Jan  does this observation make any sense? Think it could be salt?
   -Rod.

  Jan Warnqvist [EMAIL PROTECTED] wrote:
Hello Joe.
There were probably small amounts of mono- and diglycerides left in the 
biodiesel, and/or possibly soaps which together are excellent emulsifiers. A 
strong acid will divide the glycerides into fatty acids and glycerine ,and the 
soaps into salts and fatty acids, which then goes into a fat phanse and an 
aquaeus phase, possibly with the salts in the bottom.'
Best regards
Jan
  - Original Message - 
  From: Joe Street 
  To: biofuel@sustainablelists.org 
  Sent: Friday, August 10, 2007 3:45 PM
  Subject: Re: [Biofuel] Glycerine Settling Time


  Hi Jan;

  Ok your post agrees with what Andres said.  So how do we explain Tom's 
experiment then?  To recap (Tom correct me if I miss something here) he took 
washed esters that passed the methanol test and added water and (of course) no 
emulsion when agitated. Whatever mono and diglycerides were in the esters were 
small but present I assume, but yet no emusion. Then added some small quantity 
of glycerol ( which had been separated from the soaps, FFA and salts) and 
agitated again and did get an emulsion.  I have had the feeling glycerin has 
usually been the cause of emulsion problems when I have had them.  No doubt a 
poorly reacted batch is much more likely to have the problem but is that really 
due to the glycerides or is it glycerin which hasn't settled.  Remember we 
started this discussion that the glycerin settles much slower in a poorly 
completed run.

  BTW as an addition to this discussion look what someone just posted on my 
yahoo group!  Using glycerin cocktail to BREAK an emulsion.  Now that's 
radical!!?? 

  http://www.biodieselcommunity.org/breakingemulsions/

  Joe

  Jan Warnqvist wrote:

Hi evereybody. I feel obliged to enter this discussion. Pure glycerine is   not 
a good emulsifier due to the fact that there are three OH-groups and   that the 
carbon s in the first  and third positions are surronded by two   hydrogene 
atoms. This makes the glycerine hydrophilic in five places   alltogether. 
However, the mono- and diglycerides are excellent emulsifiers.   Only small 
amounts of these are sufficient to create stable emulsions. Would   somebody 
agree with me on that ?Jan Warnqvist 
 - Original Message -   From: Keith Addison [EMAIL PROTECTED]  To: 
biofuel@sustainablelists.org  Sent: Friday, August 10, 2007 9:53 AM  Subject: 
Re: [Biofuel] Glycerine Settling TimeHi TomHi Keith,  
Then if you do one-litre test batches first, especially with iffy  batches of 
oil,  Ops.I took Joe's point to be: If you have to 
re-process it is possible to  use info from the QT to determine how much (how 
little) methanol you'll   need  to use.I also took 

Re: [Biofuel] Glycerine Settling Time

2007-08-13 Thread Keith Addison
Thanks Joe.

Hi Keith;

Most often the process comes to 95% or more complete and that is 
good enough for me ( personal choice) and doesn't give me wash 
problems either.  Maybe 20% of the time it only gets to somewhere 
around 90% and this is a problem.  It tends to be most likely to 
happen when the feedstock titrates with a result of higher than 5 
(this is titrating with KOH soln rather than NaOH) which is what I 
consider borderline for going acid-base. Settling time is not less 
than 12 hours for me. 
Sorry about snipping the remainder of your post, was trying to save bandwidth.
Off for the weekend now will check messages on Monday.
Hope you are having a good weekend. And also to those about to start 
the weekend.
Tirah
Joe

Keith Addison wrote:

Hi Joe



Hi Keith;

See my answers below.

Keith Addison wrote:



Well, settling time is free.

Acid-base aside, there's the two-stage base-base process, which quite
a lot of people use and like, but otherwise why do more than one
stage? Do you mean two separate stages, with a methanol test in
between? So you process it twice? Plus extra methanol.




No,- more like aiming for a single stage and then using the methanol
test right after the settling period (after draining the glycerol of
course) it gives you a chance to hit the reactor with another small
dose of methoxide if it wasn't quite a complete reaction. The test
also tells you how much to use.  There is no standardising the
process here since the feed is never the same twice.



I don't think anybody's feedstock is ever the same twice, unless
they're getting it from a food factory with a standardised operation.
No restaurant cooks exactly the same food in the same way two days
running.

Anyway, why should that mean changing anything but the amount of
catalyst needed? That's what titration is for, no? Certainly you can
standardise the other variables.



Rod decided to try a methanol test before washing, just for giggles
and it turned out to be a heluva good idea. You know right away if
you got a good reaction without having to waste all the time energy
and water washing and drying before doing a quality test and then
potenially having to reprocess.



Before you started using this extra stage, how often did you have to
reprocess? In your previous message it sounded like it happened
regularly, and it still sounds that way.



It turns out this looks just like a two step base -base type deal.
but more like 90% of it in one step and then a polishing step.
Sometimes if your process was good you don't need to do it, but if
it turns out you were not near enough to completion it's nice to
know right away. There's still methanol in the esters at that point
(before washing) so it's advantageous to push the process further at
that point if it is necessary.


Joe



This seems to raise more questions than provide answers. There were
also some other points in my reply to Tom, eg, how long do you let
the glycerin settle before draining it and embarking on the second
stage/polishing step or whatever?

I'll put the rest of my message back, below.

Please see my reply to Tom:

http://tinyurl.com/3ccqhwhttp://tinyurl.com/3ccqhw
[Biofuel] Glycerine Settling Time

Best

Keith




Hi Joe



Tom;

It makes sense. Glycerin is an emulsifier.  Have you ever tried
dosing the batch again with a little methoxide?  After you remove
the glycerin it doesn't take much to get the last bit of the
reaction to go and settle out the remaining glycerin.  Of course
this is well known already.  Kenji and many others do straight base
catalysis as a two stage deal. You can do a methanol test of sorts
and the unreacted oil will settle out.  Then you can use the
measured amount of unreacted oil in the methanol test vial to
estimate the percentage unreacted oil in your batch and dose
accordingly with the stoichiometric amount of methoxide.  Assume
neutral oil for this calculation.  Rod and I do this regularly if
the batch fails the QT and it works like a charm.  Will save you
settling time in the long run.


Well, settling time is free.

Acid-base aside, there's the two-stage base-base process, which quite
a lot of people use and like, but otherwise why do more than one
stage? Do you mean two separate stages, with a methanol test in
between? So you process it twice? Plus extra methanol.

Why not do it in a single phase? Todd Swearingen once suggested this
here (discussing mixing pump sizes):



To judge an appropriate reaction time, pull an exact amount of fluid
(200 ml would suffice) out of the reaction stream every half-hour or
hour after an arbitrary initial ~1 hour reaction period.

Presuming that the contents of the reactor are kept homogenous from
the pump flow, the volume of the glycerol cocktail that settles out
of each sample will give you a fair gauge as to when your reaction
completed.

The suggestion would be to continue the reaction for ~1/2 hour
beyond the point where your glyc cocktail volume stabilized.


That works. 

[Biofuel] Rising temperatures will stunt rainforest growth

2007-08-13 Thread Keith Addison
http://www.nature.com/news/2007/070806/full/070806-13.html

nature.com
Published online: 10 August 2007
Rising temperatures will stunt rainforest growth
Plants suffering in the heat could make global warming worse.

Michael Hopkin

Global warming could cut the rate at which trees in tropical 
rainforests grow by as much as half, according to more than two 
decades' worth of data from forests in Panama and Malaysia. The 
effect - so far largely overlooked by climate modellers - could 
severely erode or even remove the ability of tropical rainforests to 
remove carbon dioxide from the air as they grow.

The study shows that rising average temperatures have reduced growth 
rates by up to 50% in the two rainforests, which have both 
experienced climate warming above the world average over the past few 
decades. The trend is shown by data stretching back to 1981 collected 
from hundreds of thousands of individual trees.

If other rainforests follow suit as world temperatures rise, 
important carbon stores such as the pristine old-growth forests of 
the Amazon could conceivably stop storing as much carbon, says Ken 
Feeley of Harvard University's Arnold Arboretum in Boston, who 
presented the research at the annual meeting of the Ecological 
Society of America in San Jose, California.

Losing their balance

The amount of carbon that a forest stores depends on the balance 
between the rate at which it draws carbon dioxide from the atmosphere 
through photosynthesis and the rate at which it gives carbon dioxide 
back through respiration. In carbon sinks, which are mostly found at 
high latitudes, photosynthesis outstrips respiration and the amount 
of carbon stored increases. In general, tropical forests are today 
thought to act as stable stores of carbon, with their photosynthetic 
input and their respiratory output more or less in balance.

Some scientists and environmentalists have suggested that, given the 
way carbon dioxide spurs plant growth, tropical forests could in time 
come to act as a sink, offsetting some of the man-made carbon dioxide 
build-up.

That optimism will have to be reassessed, though, if photosynthesis 
becomes less productive in the tropics. The trends measured by Feeley 
suggest that entire tropical regions might become net emitters of 
carbon dioxide, rather than storage vessels for it. The Amazon basin 
as a whole could become a carbon source, Feeley says.

Feeley and his colleagues analysed data on climate and tree growth 
for 50-hectare plots in each of the two rainforests, at Barro 
Colorado Island in Panama, and Pasoh in Malaysia. Both have witnessed 
temperature rises of more than 1ºC over the past 30 years, and both 
showed dramatic decreases in rates of tree growth. At Pasoh, as many 
as 95% of tree species were affected, Feeley and his colleagues 
report. The research has also been published in the journal Ecology 
Letters1.

Sinking feeling

Feeley suspects that the effect occurs because plant photosynthesis 
is impaired if the temperature rises above a certain threshold. The 
effect, he adds, has not been included in models of the global carbon 
cycle, meaning that predictions of the future performance of tropical 
forests as carbon stores may be unduly optimistic.

That said, he stresses that the effect is far from proven, and could 
be due to other factors. Under increasing carbon dioxide alone, we 
know the growth rate will increase, he says. But there are lots of 
factors - it's naïve to think of any one in isolation. The study 
acknowledges that increased cloudiness - or even a growing role for 
lianas - may account for some of the results.

Yet ultimately, those changes are also related to climate change, 
which can be expected to have effects all over the tropics. If we're 
correct and the temperature is driving these changes, this is 
something we're going to see in a lot more places, Feeley predicts. 
It has very important implications - we may need to look elsewhere 
for our excess carbon sink.

So far, the Amazon rainforest - the world's biggest - has not 
suffered significant climate warming. But with even the most 
optimistic predictions of climate analysts asserting temperatures are 
to rise by 2ºC over the coming century, most rainforests could feel 
the effect before too long.

©2007 Nature Publishing Group

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Re: [Biofuel] Glycerin as an Emulsifier (was Glycerine Settling Time)

2007-08-13 Thread Thomas Kelly
On Friday 8/10, I noted that:

II. Glycerin Cocktail:   Time to Separate 
(wash test)
   good quality BD + water + glycerin cocktail2 hours* 
   poor quality BD  + water + glycerin cocktail2 hours*

It almost 2 days for the good quality BD to separate out. There was a very 
clear soap layer between the BD layer and the water layer.

It's almost three days now and the poor quality BD still has an emulsion 
layer. More than half of the BD layer is emulsion. 

My thoughts:
1. Glycerin, itself, separated from the cocktail, is not an effective 
emulsifier
2. Presence of just the glycerin cocktail lengthens the time needed to  
separate water from BD
3. The glycerin cocktail in combination with even small amounts of unreacted 
Mono- and Di- Glycerides forms emulsions during wash.

***Keep in mind that my poor quality BD failed the Methanol Solubility Test 
(the Warnqvist Quality Test), in that the resulting mix was cloudy, and given 
time, an observable, but difficult to measure, amount of residue (unreacted 
glycerides) dropped out. There were not globs of residue. This was not real bad 
BD. It is used in my home heating system.

Questions/Comments:
1. Unreacted Mono- and Di- Glycerides have a reputation as being very effective 
emulsifiers. They are present in the BD that I make to heat my house. Why don't 
they form emulsions when I stir wash this BD?

2. If glycerin cocktail (unsplit) is present, the same levels of Mono- and Di- 
Glycerides form emulsions, when they are only shaken . 
Does this represent a cumulative or synergistic effect?

 The cumulative/synergistic effect of glycerin cocktail and unreacted 
glycerides on emulsion formation would explain a couple of observations:
a. Incomplete reactions coupled with short (6 - 8 hour) settling times often 
produce emulsions in the wash. Longer settling times 2 days or more 
no emulsions. The glycerin has settled out
b. After breaking emulsions (1st and even 2nd wash), subsequent washes go well 
w/o emulsions forming. The Mono- and Di-Glycerides are still present, but the 
components of the glycerin cocktail have been, for the most part washed out.

3. Does the glycerin cocktail settle out of incomplete reactions more slowly 
than from complete reactions?

Tom


- Original Message - 
  From: Thomas Kelly 
  To: biofuel 
  Sent: Friday, August 10, 2007 2:46 PM
  Subject: [Biofuel] Glycerin as an Emulsifier (was Glycerine Settling Time)


  Andres, Jan, Joe, Keith, and anyone else who has been following the saga,

   It would seem that glycerine, itself, is not an effective emulsifier. 

  I've spent the morning experimenting in the kitchen. I did Wash Tests on 
BD that passed the QT and BD that failed the QT. I tested one group with 
glycerine split from the cocktail (using Phosphoric Acid) and another group 
with unsplit Glycerin cocktail.

  Volumes used:
  Biodiesel 150 ml
  Water 150 ml
  Glycerin (split and unsplit)  4 ml

  Temp:  70F  (~22C)

  I. Glycerin split from the cocktail (used Phosphoric Acid):
 Controls:   Time for clear 
separation (min)
 good quality BD +  water  1 - 2
 poor quality BD  +  water  3 - 4

 Experimental:
 good quality BD + water + glycerine (split) less than 5
 poor quality BD  + water + glycerine (split) less than 5

  II Glycerin Cocktail:
 good quality BD + water + glycerine cocktail2 hours* 
 poor quality BD  + water + glycerine cocktail2 hours*

  * At 2 hours there is a thin layer of BD (1 - 2 mm) The rest appears to be an 
emulsion.

   Andres and Jan, you are correct. Glycerin, itself, did little to 
retard separation of BD and water.

   Something in the cocktail does seem to be an emulsifier. (The soaps??)

  Some questions remain:
  1. The BD that failed the QT (incomplete reaction) was obtained from a tank 
that feeds my heating system. It contains unreacted glycerides, but does not 
produce an emulsion when shaken in water, nor did it produce emulsions when it 
was stir-washed. Why not?
  2. At Joe Street's suggestion I took a sample of BD that had settled for 
about 10 hours. Twelve hours later, more glycerin had settled out. Today, 
still another 24 hours later, even more has settled out. Could this small 
amount of unsplit glycerine (with associated soaps) be the cause of the 
emulsions I got when I started making BD? It would explain why settling for a 
day or more seems to eliminate the problem.
  3. Does the glycerine mix (or soaps) settle out more slowly in BD from 
incomplete reactions?

   Tom




--


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[Biofuel] Analysts See 'Simply Incredible' Shrinking of Floating Ice in the Arctic

2007-08-13 Thread Keith Addison
http://www.commondreams.org/archive/2007/08/10/3105/
- CommonDreams.org
Published on Friday, August 10, 2007 by The New York Times
Analysts See 'Simply Incredible' Shrinking of Floating Ice in the Arctic

by Andrew C. Revkin

The area of floating ice in the Arctic has shrunk more this summer 
than in any other summer since satellite tracking began in 1979, and 
it has reached that record point a month before the annual ice 
pullback typically peaks, experts said yesterday.

The cause is probably a mix of natural fluctuations, like unusually 
sunny conditions in June and July, and long-term warming from 
heat-trapping greenhouse gases and sooty particles accumulating in 
the air, according to several scientists.

William L. Chapman, who monitors the region at the University of 
Illinois Urbana-Champaign and posted a Web report on the ice retreat 
yesterday, said that only an abrupt change in conditions could 
prevent far more melting before the 24-hour sun of the boreal summer 
set in September. The melting rate during June and July this year 
was simply incredible, Mr. Chapman said. And then you've got this 
exposed black ocean soaking up sunlight and you wonder what, if 
anything, could cause it to reverse course.

Mark Serreze, a sea-ice expert at the National Snow and Ice Data 
Center in Boulder, Colo., said his center's estimates differed 
somewhat from those of the Illinois team, and by the ice center's 
reckoning the retreat had not surpassed the satellite-era record set 
in 2005. But it was close even by the center's calculations, he said, 
adding that it is almost certain that by September, there will be 
more open water in the Arctic than has been seen for a long time. Ice 
experts at NASA and the University of Washington echoed his 
assessment.

Dr. Serreze said that a high-pressure system parked over the Arctic 
appeared to have caused a triple whammy - keeping away clouds, 
causing winds to carry warm air north and pushing sea ice away from 
Siberia, exposing huge areas of open water.

The progressive summertime opening of the Arctic has intensified a 
longstanding international tug of war over shipping routes and 
possible oil and gas deposits beneath the Arctic Ocean seabed.

Last week, Russians planted a flag on the seabed at the North Pole. 
On Wednesday, Stephen Harper, the Canadian prime minister, began a 
tour of Canada's Arctic holdings, pledging to vigorously protect our 
Arctic sovereignty as international interest in the region increases.

© 2007 The New York Times

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Re: [Biofuel] Glycerin as an Emulsifier (was Glycerine Settling Time)

2007-08-13 Thread Joe Street

Hi Tom;

If the answers to questions 2 and 3 are yes then it would explain a 
lot.  Then the anwer to question one could be that although the BD did 
not pass the QT if it was settled long enough that there is no glycerol 
it would be consistent with the emergent theory. No?



Joe

Thomas Kelly wrote:


On Friday 8/10, I noted that:
 
II. Glycerin Cocktail:   Time to 
Separate (wash test)

   good quality BD + water + glycerin cocktail2 hours*
   poor quality BD  + water + glycerin cocktail2 hours*
 
It almost 2 days for the good quality BD to separate out. There was 
a very clear soap layer between the BD layer and the water layer.
 
It's almost three days now and the poor quality BD still has an 
emulsion layer. More than half of the BD layer is emulsion.
 
My thoughts:
1. Glycerin, itself, separated from the cocktail, is not an 
effective emulsifier
2. Presence of just the glycerin cocktail lengthens the time needed to 
separate water from BD
3. The glycerin cocktail in combination with even small amounts of 
unreacted

Mono- and Di- Glycerides forms emulsions during wash.
 
***Keep in mind that my poor quality BD failed the Methanol 
Solubility Test (the Warnqvist Quality Test), in that the resulting 
mix was cloudy, and given time, an observable, but difficult to 
measure, amount of residue (unreacted glycerides) dropped out. There 
were not globs of residue. This was not real bad BD. It is used in my 
home heating system.
 
Questions/Comments:
1. Unreacted Mono- and Di- Glycerides have a reputation as being very 
effective emulsifiers. They are present in the BD that I make to heat 
my house. Why don't they form emulsions when I stir wash this BD?
 
2. If glycerin cocktail (unsplit) is present, the same levels of Mono- 
and Di- Glycerides form emulsions, when they are only shaken .

Does this represent a cumulative or synergistic effect?
 
 The cumulative/synergistic effect of glycerin cocktail and 
unreacted glycerides on emulsion formation would explain a couple of 
observations:
a. Incomplete reactions coupled with short (6 - 8 hour) settling times 
often produce emulsions in the wash. Longer settling times 2 days or 
more 

no emulsions. The glycerin has settled out
b. After breaking emulsions (1st and even 2nd wash), subsequent washes 
go well w/o emulsions forming. The Mono- and Di-Glycerides are still 
present, but the components of the glycerin cocktail have been, for 
the most part washed out.
 
3. Does the glycerin cocktail settle out of incomplete reactions more 
slowly than from complete reactions?
 
Tom
 
 
- Original Message -


*From:* Thomas Kelly mailto:[EMAIL PROTECTED]
*To:* biofuel mailto:Biofuel@sustainablelists.org
*Sent:* Friday, August 10, 2007 2:46 PM
*Subject:* [Biofuel] Glycerin as an Emulsifier (was Glycerine
Settling Time)

Andres, Jan, Joe, Keith, and anyone else who has been following
the saga,
 
 It would seem that glycerine, itself, is not an effective

emulsifier.
 
I've spent the morning experimenting in the kitchen. I did Wash

Tests on BD that passed the QT and BD that failed the QT. I
tested one group with glycerine split from the cocktail (using
Phosphoric Acid) and another group with unsplit Glycerin cocktail.
 
Volumes used:

Biodiesel 150 ml
Water 150 ml
Glycerin (split and unsplit)  4 ml
 
Temp:  70F  (~22C)
 
I. Glycerin split from the cocktail (used Phosphoric Acid):

   Controls:   Time for
clear separation (min)
   good quality BD +  water  1 - 2
   poor quality BD  +  water  3 - 4
 
   Experimental:

   good quality BD + water + glycerine (split) less than 5
   poor quality BD  + water + glycerine (split) less than 5
 
II Glycerin Cocktail:

   good quality BD + water + glycerine cocktail2 hours*
   poor quality BD  + water + glycerine cocktail2 hours*
 
* At 2 hours there is a thin layer of BD (1 - 2 mm) The rest

appears to be an emulsion.
 
 Andres and Jan, you are correct. Glycerin, itself, did

little to retard separation of BD and water.
 
 Something in the cocktail does seem to be an emulsifier.

(The soaps??)
 
Some questions remain:

1. The BD that failed the QT (incomplete reaction) was obtained
from a tank that feeds my heating system. It contains unreacted
glycerides, but does not produce an emulsion when shaken in water,
nor did it produce emulsions when it was stir-washed. Why not?
2. At Joe Street's suggestion I took a sample of BD that had
settled for about 10 hours. Twelve hours later, more glycerin
had settled out. Today, still another 24 hours 

Re: [Biofuel] Analysts See 'Simply Incredible' Shrinking of Floating Ice in the Arctic

2007-08-13 Thread Fred Oliff

Might I bring to the group's attention a four-part feature on NBC this week on the Katie Couric "show". An NBC reporter was aboard the Canadian icebreaker "pride of the fleet" Louis S. St. Laurent as it plied Canada's Northwest Passage. Starts at 1830 EDT. Try to tune in, I will. Starts tonight, ends Saturday night.




From:Keith Addison [EMAIL PROTECTED]Reply-To:biofuel@sustainablelists.orgTo:biofuel@sustainablelists.orgSubject:[Biofuel] Analysts See 'Simply Incredible' Shrinking of Floating Ice in the ArcticDate:Tue, 14 Aug 2007 03:41:52 +0900http://www.commondreams.org/archive/2007/08/10/3105/- CommonDreams.orgPublished on Friday, August 10, 2007 by The New York TimesAnalysts See 'Simply Incredible' Shrinking of Floating Ice in the Arcticby Andrew C. RevkinThe area of floating ice in the Arctic has shrunk more this summerthan in any other summer since satellite tracking began in 1979, andit has reached that record point a month before the annual icepullback typically peaks, 
experts said yesterday.The cause is probably a mix of natural fluctuations, like unusuallysunny conditions in June and July, and long-term warming fromheat-trapping greenhouse gases and sooty particles accumulating inthe air, according to several scientists.William L. Chapman, who monitors the region at the University ofIllinois Urbana-Champaign and posted a Web report on the ice retreatyesterday, said that only an abrupt change in conditions couldprevent far more melting before the 24-hour sun of the boreal summerset in September. "The melting rate during June and July this yearwas simply incredible," Mr. Chapman said. "And then you've got thisexposed black ocean soaking up sunlight and you wonder what, ifanything, could cause it to reverse course."Mark 
Serreze, a sea-ice expert at the National Snow and Ice DataCenter in Boulder, Colo., said his center's estimates differedsomewhat from those of the Illinois team, and by the ice center'sreckoning the retreat had not surpassed the satellite-era record setin 2005. But it was close even by the center's calculations, he said,adding that it is almost certain that by September, there will bemore open water in the Arctic than has been seen for a long time. Iceexperts at NASA and the University of Washington echoed hisassessment.Dr. Serreze said that a high-pressure system parked over the Arcticappeared to have caused a "triple whammy" - keeping away clouds,causing winds to carry warm air north and pushing sea ice away fromSiberia, exposing huge areas of open water.The 
progressive summertime opening of the Arctic has intensified alongstanding international tug of war over shipping routes andpossible oil and gas deposits beneath the Arctic Ocean seabed.Last week, Russians planted a flag on the seabed at the North Pole.On Wednesday, Stephen Harper, the Canadian prime minister, began atour of Canada's Arctic holdings, pledging "to vigorously protect ourArctic sovereignty as international interest in the region increases."© 2007 The New York Times___Biofuel mailing listBiofuel@sustainablelists.orghttp://sustainablelists.org/mailman/listinfo/biofuel_sustainablelists.orgBiofuel at Journey to Forever:http://journeytoforever.org/biofuel.htmlSearch the combined Biofuel 
and Biofuels-biz list archives (50,000 messages):http://www.mail-archive.com/biofuel@sustainablelists.org/


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[Biofuel] $1-billion worth of water pouring out of leaking lines - Niagara Falls Review - 2007.07.12

2007-08-13 Thread Darryl McMahon
$1-billion worth of water pouring out of leaking lines
Thu 12 Jul 2007
Page: A6
Section: Local
Byline: James Wallace
Source: Osprey News Network; Review
As much as $1 billion worth of drinking water
disappears into the ground each year from rotting,
leaky municipal water pipes, says the Ontario Sewer
and Watermain Construction Association.
Twenty to 40 per cent of all the water pumped
through municipal water systems never reaches
consumer taps. In Niagara Falls, this kind of loss
accounts for about 16 per cent of the water the city
buys from the region's treatment plants, city officials
told The Review earlier this year.
It means 84 per cent of the water the city buys
actually makes it to the faucet. In Fort Erie, water
losses are about 28 per cent, but they were as high as
35 per cent in the 1990s.
What it means is we're paying for water we're not
using and is not coming to our taps, Niagara Falls
Mayor Ted Salci said.
The watermain association recently estimated leaking
lines cost $1 billion.
I think it's something the public should be aware of,
said watermain executive director Frank Zechner.
It's a figure that would shock and outrage most
consumers, said Conservative leader John Tory. If
you told people that 20 per cent or more of the
electricity they were paying for in their house was
never putting on a light, was never running their TV,
was just going off into the air, I mean they'd be
outraged at that and demand it be fixed immediately.
Water losses are a common problem in cities, said
Niagara Falls community services director Ed
Dujlovic. Over time, cracks will emerge. If you get
it down to 10 per cent, you're doing really well, he
said in February.
Salci often talks about the need to spend public
money on infrastructure like water mains. Niagara
Falls has been spending record amounts on
infrastructure in the last few years. But the city could
use help from the federal or provincial government,
he said.
City officials are exploring the use of a new
trenchless technology that would seal cracks by
inserting a coating like a long balloon that hardens
and fixes the crack, Salci said.
NDP critic Peter Tabuns said the fact municipalities
are wasting such enormous amounts of water through
leaky pipes undermines the water conservation
message they are delivering.
Ontario officials said Wednesday the $1 billion
estimate of waste calculated by the watermain
association is not surprising.
It does fit in with some of the anecdotal evidence
we've been hearing, said Amy Tang, a spokesman
for Public Infrastructure Renewal Minister David
Caplan.
The province has invested millions of dollars to
upgrade water systems, particularly smaller ones,
Tang said.
The watermain association called on government to
invest $34 billion in repairs over the next 15 years.
James Wallace is Queen's Park bureau chief for
Osprey News Network. Contact the writer at
[EMAIL PROTECTED]
(c) 2007 Osprey Media Group Inc. All rights reserved.

-- 
Darryl McMahon
It's your planet.  If you won't look after it, who will?

The Emperor's New Hydrogen Economy (now in print and eBook)
http://www.econogics.com/TENHE/

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Re: [Biofuel] $1-billion worth of water pouring out of leaking lines - Niagara Falls Review - 2007.07.12

2007-08-13 Thread Paul S Cantrell
Funny thing, that's not funny is, about 50% of the energy contained in
coal makes it to the power outlet.

The rest is lost to heat loss, line losses and transformer losses.

On 8/13/07, Darryl McMahon [EMAIL PROTECTED] wrote:
snip
 I think it's something the public should be aware of,
 said watermain executive director Frank Zechner.
 It's a figure that would shock and outrage most
 consumers, said Conservative leader John Tory. If
 you told people that 20 per cent or more of the
 electricity they were paying for in their house was
 never putting on a light, was never running their TV,
 was just going off into the air, I mean they'd be
 outraged at that and demand it be fixed immediately.
snip

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Re: [Biofuel] $1-billion worth of water pouring out of leaking lines - Niagara Falls Review - 2007.07.12

2007-08-13 Thread Kirk McLoren
yes, but they represent reasonable engineering. The water mains are deferred 
maintenance. A different kind of engineering I suppose.

Paul S Cantrell [EMAIL PROTECTED] wrote:  Funny thing, that's not funny is, 
about 50% of the energy contained in
coal makes it to the power outlet.

The rest is lost to heat loss, line losses and transformer losses.

On 8/13/07, Darryl McMahon wrote:

 I think it's something the public should be aware of,
 said watermain executive director Frank Zechner.
 It's a figure that would shock and outrage most
 consumers, said Conservative leader John Tory. If
 you told people that 20 per cent or more of the
 electricity they were paying for in their house was
 never putting on a light, was never running their TV,
 was just going off into the air, I mean they'd be
 outraged at that and demand it be fixed immediately.


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[Biofuel] Canadian cities worried about fluoride shortage - Regina Leader-Post - 2007.08.11

2007-08-13 Thread Darryl McMahon
Thought this would be of interest as we have discussed fluoridation 
before, and other dental practices.

 Original Message 

Canadian cities worried about fluoride shortage
Sat 11 Aug 2007
Page: A10
Section: News
Byline: Bill Mah and William Lin
Dateline: EDMONTON
Source: CanWest News Service
EDMONTON -- Cities and towns across Canada and
the United States are scrambling for supplies of
fluoride -- a chemical they add to their water systems
to prevent tooth decay.
Ottawa has been without the additive for extended
periods in recent months because of a global
shortage.
The shortage has stirred debate over a decades-old
practice, with critics flashing big, toothy grins at the
prospect of cities stopping fluoridation, something
they say does more harm than good to our health.
It's an excellent thing for them to be short of this
chemical, said Paul Connett, executive director of
the U.S.-based Fluoride Action Network.
If having a shortage of it makes them question the
practice, that would be very, very good.
Ottawa's fluoride comes from East Tampa, Fla., and
its shortage has been attributed to Hurricane Katrina
damaging Gulf Coast manufacturing facilities two
years ago, a downturn in the phosphate mining
industry and the shutdowns of some American
suppliers.
In the past year, prices have doubled for the
dwindling supply of fluoride, a byproduct of
phosphate mining, said Dixon Weir, Ottawa's
manager of drinking water services.
There have been problems noted with the supply
chain. We are aware that there are shortages that have
been reported in other communities, Weir said.
Edmonton is one of those communities, with a
fluoride shortfall looming this fall if an expected
shipment falls through.
At this time, we have sufficient fluoride to meet
Edmonton's needs until the fall, said Mike Gibbs,
spokesman for Epcor, which supplies water to the
region.
But it is a situation we're closely monitoring and
actually what's happening is there's a shortage in
North America of fluoride.
U.S. cities as diverse as New Orleans, Portland,
Maine, and Greensboro, N.C. have reported shortages
or temporarily suspended water fluoridation.
Fluoridation has long been promoted by dentists, and
by the Canadian Dental Association, as a
cost-effective and far-reaching way to prevent tooth
decay for the public.
According to Health Canada, many studies show
fluoridated water greatly reduces the number of
cavities in children's teeth.
However, the practice has long had its share of
detractors.
The Fluoride Action Network released a statement
this week signed by more than 600 professionals --
including more than 100 dentists -- calling for an end
to water fluoridation.
They say while using fluoride in toothpaste has
proven effective in preventing tooth decay, putting it
in the water supply has shown minimal benefits.
It makes as much sense as swallowing sunblock,
said Connett.
His group says the detrimental effects of fluoride
include an increased risk of bone fractures, lowered
IQ, decreased thyroid function and a staining of teeth.
About 40 per cent of Canadians receive fluoridated
water.
This spring, the Quebec government was urged to
force the City of Montreal to fluoridate its water
supply and end what it described as an epidemic of
tooth decay among the city's preschoolers.
Some towns, including Kamloops, B.C., and Cobalt,
Ont., have stopped fluoridating their water over the
years.
Kimberly Carriere, spokeswoman for the Alberta
Dental Association, said going without fluoridated
water for short periods isn't likely to harm dental
health.
For long periods, you'd certainly see an increase in
dental (decay) but you do have fluoride in your
toothpaste so the impact wouldn't be that large in the
short term, Carriere said.
Edmonton Journal and Ottawa Citizen

-- 
Darryl McMahon
It's your planet.  If you won't look after it, who will?

The Emperor's New Hydrogen Economy (now in print and eBook)
http://www.econogics.com/TENHE/

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