Hi John, Paul,
I keep trying to say this. Pyrolysis of biomass has two distinct thermodynamic stages. The first is "endothermic", where input of external heat is required in order to bring the temperature of the feedstock up high enough, so that the second "exothermic" stage can begin. This requires heating the biomass up through about ~250-300C. In the "exothermic" stage, the pyrolyzing biomass is being converted into both charcoal and liberated gases, {H2, CO, CH4, CO2, H2O}. Additionally (this is the important point I have been trying to make), in the exothermic stage, there is no need to continue to supply external heat. The reaction itself provides enough heat to be self-sustaining at that point, as long as there is a supply of oxygen. The supply of oxygen is limited to prevent the char/feedstock bed from bursting into flames, ie. complete combustion (complete oxidation).
The biomass begins to eject flammable gases {H2, CO, CH4} instead of complete combustion gases {CO2, H2O} because the oxygen is limited.
But, there is plenty of heat. Adding heat will not accelerate this process, nor prevent the consumption of more charcoal Carbon. The only mechanisms that can do that are things like throttling back the inflow of oxygen, or removing the charcoal/biomass from the pyrolysis zone (ie. suffocate and cool the charcoal/feedstock).
This means that wrapping the gases back around to heat the pyrolysis zone is pretty much useless. The gases could be used to pre-heat or dry a cool wet feedstock, but this really needs a slower heating rate to do well, and combustion of the flammable component of the pyrolysis gases is much hotter than needed for this purpose. There are better uses for the chemical energy found in these gases and/or the quality of "sensible" heat that can be generated by combusting these gases.
Capturing the liberated pyrolysis gases is the best way to capture some of the "bio-energy" that is made available via pyrolysis of biomass.
Once pyrolysis and liberation of these gases is occurring, then throwing it back into the reactor would be as much a waste as FLARING it off above the reactor. Finding a real "use" for the energy is a better approach, I think.
Regards,
SKB
----- Original Message -----
From: John SeedSent: Thursday, October 23, 2008 4:32 AMSubject: Fw: [biochar] low cost/tech clean charcoal
----- Original Message -----John: The important goals are to produce char:From: Paul Taylor
- with good conversion quality of feedstock to char
- cleanly in terms of ghg and visual and environmental pollution
- efficiently in terms of utilization of waste heat
- low tech, low cost, replicable design
- others such as quality of char
As I see it the conversation with Sean seemed to be moving in divergent directions: you would like to consume the waste heat towards charring the feedstock, whereas Sean is concerned to get a clean burn such as in a TLUD. Below I tried to recapture my original post aimed at clarifying that, and ended up thinking out loud.
-----------
In my understanding of method Sean was describing, TLUD, the primary air for pyrolysis is drawn in the bottom of the drum and supports pyrolysis which starts at the top of the drum and progresses downwards as the material is charred. The air flow is limited to avoid burning char at or above the pyrolysis zone. Ample secondary air is admitted at the top of the barrel to flame the off-gasses in the chimney. In this method the energy for pyrolysis comes from the feedstock, and the off-gasses are fully flamed. Energy from the secondary burning can be captured and utilized in any number of ways from simple hot water, hot tub, heating, drying or processing around the home or farm. In a more high tech development they could be converted to electricity using thermoelectrics.
This two stage process gives two burning zones of different temperatures with separate control over the limited O2 needed for charring and the ample O2 needed for flaming, but with some drop in efficiency of char output due to some C being used to drive pyrolysis. In fact I understand conversion efficiency seems to be limited to about 20%. Trying to combine the two functions can lead to compromise and loss of efficiency in other ways. My earlier innovation was to draw off the off-gas and bring it into the bottom of the barrel. The fuel in the off-gasses would then burn at the pyrolysis front and save some C from the feedstock. The problem is to recirculate the off-gas down past the drum (this could be via a jacket which warms the inner drum) and reinject it at the bottom with the right amount of fresh air to support pyrolysis. The immediate concern is some of the off-gasses require a higher temperature to oxidize and I don’t know how one could preferentially vent and flame those.
An alternative would be to fully flame the off-gasses in the normal TLUD process but to exchange the heat produced into the kiln drum, example by clean burning the off-gasses below and around the drum. This seems to be more or less what you are looking for, and moves in the direction of cooking the wood. The simple version is a Folke Günther double drum kiln. In my preliminary understanding the process is initiated by building a fire in the outer drum, which then drives off wood gasses from wood in the inner drum through holes which feed the fire in the outer drum. With enough air supply and a bit if canny design this should result in complete combustion, and limited extra fuel to initiate the reaction.
I can think of an interesting idea involving a triplet of nested drums. The inner drum, open at the top, contains the batch of feedstock. The intermediate drum, open at the bottom carries the off-gassing to the outer drum, open at the top. The bottom of the outer drum has an air feed and it is mounted by a chimney. Once pyrolysis is proceeding the off-gassing feeds a fire in the outer drum, which provides heat for the pyrolysis. The problem is starting the pyrolysis. If necessary one could use a two stage process so that the smaller primary stage would be started with less fuel and could ignite the secondary stage. In fact the primary stage could be a TLUD since these are efficient to start and clean burning, and the secondary stage could be a perforated drum of feedstock in the “chimney” of the primary. I think conversion efficiencies of 40% might be achieved in some version of this.
I am sure all this is part of the art for those skilled in it. I do see that with the grant, and some care in remaining flexible in our initial design, there could be considerable room for innovation. In short I agree that we should pursue innovation in the area of low tech recycling of the flame off heat to the pyrolysis, since recycling it into hot water etc is a known art.
Paul
On 10/22/08 2:18 AM, "John Seed" <johnseed1@ozemail.com.au > wrote:
Hi Paul, thats right, if you could usefully use the heat, then less of a problem flaring the gasses in the flue rather than using them to power the pyrolysis. I see this as "plan b" however, a fall back if we can't figure out a low tech way to reliably get enough oxygen to the pyrolysis exhaust gasses while they're still in a place to power the reaction. Do you agree?
for the Earth
John
----- Original Message -----
From: Paul Taylor <mailto:potaylor@bigpond.com >
To: John Seed <mailto:johnseed1@ozemail.com. >au
Sent: Tuesday, October 21, 2008 8:49 AM
Subject: Re: [biochar] low cost/tech clean charcoal
John: This recommendation comes back to the TLUD stoves. A low tech addition to such a stove would be to use the heat generated in the chimney for hot water, a welcome hot tub, home heating, farm process heat, or - higher tech – refrigeration or using thermoelectrics to generate electricity. Does any of this fit with your chosen method? In the long run mainstream application it is easy to see how the excess energy can be retrieved/used in one form or another, and it would be nice to illustrate a low tech version of that from the beginning
Paul
On 10/20/08 1:57 PM, "Sean K. Barry" <sean.barry@juno.com > wrote:
Hi John,
A barrel with holes in the bottom of it, that is "cooked" (if you will allow this description) over another open flame will have the gases from the heated internal contents of the barrel ejecting out in the places where it is easiest to get out. This would be (possible, only) out through the holes at the bottom. Getting oxygen supplied, past the heating flames, to the gases that are ejecting from the bottom of the barrel would be the trick. It will fan the flames of the heating fire and leave little oxygen to combust the gases. The off gases, too, being ejected this way flow counter to the natural draught of the heat.
I would suggest primary air inlet holes around the outside bottom of the barrel, a chimney above a conical top for the barrel, and secondary air inlet holes (with more cross-section area than the primary inlets) around the base of the chimney, bottom of the cone top, or top outside rim of the barrel. The draught will suck air in through both the primary inlet holes and the secondary inlet holes (more through the secondary inlets). Providing primary air to the pyrolizing biomass inside the barrel will actually produce more solid charcoal byproduct, less liquids, and (depending on the amount of primary air) more gases as reaction products. Insulate the barrel (and chimney if you can) with refractory brick or other high temperature insulation, then make sure that there are flames inside the chimney and this will assure that most all of the flammable off gases are being burned before they exit the chimney.
The main flaws in the type of design I suggest would be more complete combustion of the raw biomass (meaning lower charcoal yield) and significant loss of what might be otherwise useful energy in the form of lost heat (up the chimney).
Regards,
SKB
----- Original Message -----
From: John Seed <mailto:johnseed1@ozemail.com. >au
To: biochar@yahoogroups.com
Sent: Thursday, October 16, 2008 4:01 AM
Subject: Re: [biochar] low cost/tech clean charcoal
Hi Sean,
you wrote: <<The important issue to achieve this performance (no or little release of GHGs) is to provide sufficient secondary air to mix with the off gases exiting from the pyrolysis reaction vessel.>>
I'm wondering whether you could do this with a single 44 by surrounding it with brick or clay insulation so that most of the escaping heat goes up a chimney and then somehow use that heat to drive a fan pushing air under the 44 to make sure that there's enough oxygen to burn all the gasses exiting the drum there?
for the Earth
John
----- Original Message -----
From: Sean K. Barry <mailto:sean.barry@juno. >com
To: biochar@yahoogroups.com
Sent: Thursday, October 16, 2008 12:55 AM
Subject: Re: [biochar] low cost/tech clean charcoal
Hi John,
I appreciate your concern. However, I think that you doing useful experiments using biochar in your garden may be worth making some charcoal however you see fit to do it. Folke's barrel within a barrel retort is one possibility. It may or may not entirely burn the off gases. I can't say that I really know that it does or doesn't either way, without testing this somehow. I just understand the desired performance.
The important issue to achieve this performance (no or little release of GHGs) is to provide sufficient secondary air to mix with the off gases exiting from the pyrolysis reaction vessel. This would be something like several larger holes around the top of the outside barrel, more and larger holes than at the bottom.
TLUD stoves also have large secondary air entry vents at the base of the chimney. THe draught created in the chimney serves to "suck in" this secondary air. It also pulls air in the bottom holes. This is why you would want smaller and fewer holes at the bottom than at the top (or base of the chimney).
Pyrolysis reactions go through different "energy input vs output" phases during the rise in temperature. From ambient temperature up to about 250-300C, the reaction is said to be endothermic. This means it needs a continuous input of heat from an external source in order to continue its rise in temperature. Once the pyrolysis reaction has begun to expel gases, the reaction becomes exothermic. It generates enough heat to be self sustaining, even without the application of external heat. The only input need is a limited oxygen supply, not heat. If too much oxygen is supplied, then the biomass will burst into flames and combustion will be occurring. Really, it is just more complete combustion and more heat is generated.
As the fuel in the biomass "burns" during combustion, gases, liquids, and solids are all being expelled from the feedstock very vigorously. Things are literally exploding off the surfaces that are engulfed in flames. Where the temperatures are high enough and there is sufficient oxygen that has not already been consumed, then fuel combines with oxygen and generates more heat. But, throughout this vigorous production of energy and expelling of matter, some things fly through places without enough oxygen or without enough heat and they do not combust. This is the smoke, the tars, and the gases. Even large roaring fires don't burn everything. It there is smoke then there is fire, but the smoke is evidence that some things have not burned. It there is heat, but no smoke, then there is still fire, and it is more complete combustion.
The same is true of gases, liquids, and solids exiting from a pyrolysis reactor. More fuels exit, too, because the oxygen supply is being limited. Oxygen is supplied just enough to sustain the reaction, but there is no explosive combustion occurring. So, gases once vented from the reactor need two things to be "completely combusted", more oxygen and enough heat to ignite the combustion. If the oxygen near the bottom is being limited, then that cannot be the secondary source of oxygen. A true second input of oxygen is required and it cannot go to the pyrolyzing biomass inside the reactor vessel. It has to mix with the escaping producer gas. Then this mixture needs to be ignited. If there is no flame above the reactor or in the chimney above the reactor, if there is "blue smoke", then the gases, vaporized liquids, and particulate solids are being "liberated" without being consumed. This is when Methane-CH4 can be vented.
Regards,
SKB
----- Original Message -----
From: John Seed <mailto:johnseed1@ozemail.com. >au
To: biochar@yahoogroups.com
Sent: Wednesday, October 15, 2008 3:29 AM
Subject: Re: [biochar] low cost/tech clean charcoal
Hi Sean, thanks for the further clarification.
I'd like to make some biochar to start conducting trials in my garden and orchard. However, I don't want to do so if this means releasing methane.
The descriptions I've seen of Top-Lift-Updraft (such as at http://terrapreta.bioenergylists. ) appear to ensure that there is enough oxygen to burn the methane etc but at the cost of wasting the heat as these gases burn in the chimney.org/taxonomy/ term/89
What I like about burning these gasses beneath the drum in which the charcoal is being made, (if I understand this correctly) is that if the drum is well insulated, the burning gasses could provide enough heat to drive the whole process (once burning wood has heated the drum and contents sufficiently to begin expelling the gasses in the first place). So, less fuel would need to be burned to drive the pyrolysis and less CO2 produced.
However, as you say, you'd need to design the thing so that there was always enough oxygen being sucked into the space below the drum to ensure that all the gasses combusted.
Problem is, how would you know that there were no uncombusted gasses escaping without expensive testing equipment?
Of course if you had a way of utilising the heat coming out from the Top-Lift-Updraft stove because you were cooking and charcoal was just a byproduct or some other way of making the heat do some work, that might give an efficient solution.
John Seed
----- Original Message -----
From: Sean K. Barry <mailto:sean.barry@juno. >com
To: biochar@yahoogroups.com
Sent: Wednesday, October 15, 2008 1:16 AM
Subject: Re: [biochar] low cost/tech clean charcoal
Hi John,
See my comments to this post below.
Thanks so much for that clear reply concerning the chemistry of pyrolysis
Sean. SKB: You're welcome. I hope it was not too technical or confusing.
If I make charcoal using a sealed 44 gallon drum with holes in the bottom to
allow the gasses to escape but little oxygen to enter and a fire underneath,
then will all the escaping methane necessarily be consumed? SKB: This is kind of hard to answer. It depends greatly upon the amount of oxygen available and the amount of fuel be vented from the 44 gallon drum. Secondary combustion is not complete if there is not sufficient oxygen. When you say there is a fire underneath, there is consumption of oxygen occurring right there where the holes are. I suppose that if you see jets of flame shooting out of the holes in the bottom of the drum that you could assume that at least some of the offgas is also being consumed. But, if there is not enough oxygen left after the fire below consumes the oxygen, then some of the fuel gases (H2, CO, CH4) will exit hot and leave the area where ignition is still possible before there is sufficient oxygen for it to burn.
If you think about a fire made of wood, there are times when there are lots of flame, but right in the middle of the flame there still sits some unburned wood. That is fuel, too, like the gases H2, CO, and CH4. That wood "sitting" inside the flames just has not burned yet. There is not enough oxygen there yet to burn it. In fact, sometimes over a campfire, for instance, you can shove a dry stick right into a flame and pull it back out, over and over again, roasting marshmellows. It doesn't burn. This is basically because inside the flame, there is not enough oxygen or enough time at the ignition temperature, or both, for consumption to occur.
You wrote that <<Pyrolytic reactions do not emit Sulfur Oxides-SOx, Nitrogen
Oxides-NOx (specifically NO, NO2, NO3), nor Nitrous Oxide-N2O. The only of
these which is a GHG is N2O. The temperatures of pyrolysis, 400C to 600C,
are just not hot enough to form these compounds>>
Given that there's no way to control the temperature using this method and
that the temperature is going to rise above 600C, will N2O be produced?
SKB: N2O is produced via a completely other pathway, involving the nitrification/de-nitrification cycle in soil amended with nitrogen fertilizers. Temperatures for NOx are still higher than what can be achieved with low oxygen flow and at atmospheric pressure, like that occurring in the kind of pyrolysis reaction you are using. If the pressures were substantially higher or the temperatures like those inside the flame front of a gasoline burn at 11:1 compression inside an internal combustion engine (I'm guessing here, but maybe 1500C+, then concern over generating NOx might be warranted.
You wrote <<The most significant problems creating "non-clean" GHG emissions
from a pyrolysis reaction done in a low cost/low tech reactor/kiln would be
to NOT BURN (or FLARE) any Methane-CH4 exiting from the reactor or to be so
inefficient as to release more carbon in the "producer gas" (as CO, CO2, or
CH4) than is left in the charcoal by-product. The main reason not releasing
Methane-CH4 is that it is such a potent GHG. It is 23 times more potent
than CO2 in the atmosphere.>>
Assuming that the methane necessarily flares in the woodfire beneath the 44,
what would be any other factors that might make this process <<be so
inefficient as to release more carbon in the "producer gas" (as CO, CO2, or
CH4) than is left in the charcoal by-product.>> SKB: I think it is difficult to determine that the Methane necessarily flares in the woodfire beneath. Have you heard of the terms "rich" and "lean" with regard to how an internal combustion engine is running? "Rich" means there is more oxygen being supplied to the combustion zone than is required to completely burn the fuel. "Lean" means the opposite, so some fuel exits the engine unburnt. Many modern engines in automobiles have what are called Lambda sensors (or oxygen sensors) These device sense the amount of oxygen left in that exhaust stream that is exiting the engine. If there is excess oxygen, then the air/fuel ratio (the lambda) can be adjusted up. If there is more oxygen, then the air/fuel ratio can be adjusted down. This way the engine can automatically regulate the efficiency of the combustion process.
With your "sealed" 44 gallon drum that only has holes in the bottom of it, there is no draught and no independent secondary air entry point. All of the oxygen that is used for the fir below, the flaming pyrolyis within, and the consumption of the exiting offgases enters from below the barrel. Unless you have this barrel elevated and are blowing air or oxygen directly at the bottom, then I suspect there is not sufficient oxygen coming in to consume all of the wood in the fire below plus the exiting off gases. However, I am not there to measure the gas inflows and outflows.
I guess I'm wondering if there's any way to make this low tech method so
that I can feel assured that what I'm doing is greenhouse friendly? SKB: The short answer would be I don't know. Low tech might be workable if the design of the reactor/kiln , with air in flows and gas out flows are all known or well understood. Some make claims that Top-Lit-Updraft (TLUD), or stratified air-blown, downdraft reactors "work better". But "work better" is a subjective term, work better at producing gas is not the same thing as work better at not emitting GHGs. Work better at generating usable heat is not the same thing as work better at producing more charcoal. I suppose it is possible that some people with excellent educations and experience at thermodynamis and the biochemistry of wood combustion could specify as design for a low-tech solution for a kiln that produces a high yield of charcoal and vents little or no GHGs, but I do not know of one which has been proven. The techniques for analysis and/or the equipment required to sufficiently analyze any particular design are likely not entirely LOW-EXPENSE/LOW-TECH.
I read a lot about this particular topic from people who maybe could know this stuff, People like Tom Reed and Aqua Das from the Biomass Energy Foundation (see woodgas.com). But, honetsly, I can't say that I know enough about this yet to beable to say what kind of kiln/reactor/ retort design will do what you are asking. I'm still just learning and struggling with how to do this myself.
Regards,
SKB
thanks
John
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