Dear Crispin,

I was just thinking it would be a simple set up that would take an average of 
the gases collected at a single point and then see how well that correlates 
with the findings of gas readings taken directly. Sloshing water acts as a 
filter. Just a double check of the results you are surprised to see. 

 

Regards

 

Frank

 

Frank Shields

Control Laboratories; Inc.

42 Hangar Way

Watsonville, CA  95076

(831) 724-5422 tel

(831) 724-3188 fax

[email protected]

www.controllabs.com

 

 

 

 

From: Stoves [mailto:[email protected]] On Behalf Of 
[email protected]
Sent: Wednesday, September 18, 2013 1:06 PM
To: [email protected]
Subject: Re: [Stoves] Charcoal stove design

 

Dear Frank 

 

A combustion analyser does what you suggest in a continuous manner at a typical 
flow of 1 to 1.5 litres per minute. 

 

The only draw back is a delay between the sample entering the metal pipe and 
the reading on the gas detection cell. With filters along the way (introducing 
a smoothing effect on the concentration) it can take a while - perhaps 1 
minute. 

When moving the sample pipe around the gases can be determined at each 
location. Remember that gasses will react instead the sampling system so it is 
not 100% representative of reality. 


Precisely what is happening in the fire isn't critical. It is really complex. 
Something like 450 reactions are involved. ‎

 

Regards 

Crispin heading south 

>>Q10>>>


From: Frank Shields

Sent: Thursday, September 19, 2013 03:44

To: 'Discussion of biomass cooking stoves'

Reply To: Discussion of biomass cooking stoves

Subject: Re: [Stoves] Charcoal stove design

 

Dear Crispin and Saastamoinen,

 

With the GEK I work with I have control of the air and a good long bed of char 
to work with. But what is the goal of these small household stoves? Perhaps 
with natural draft? I would think a surface reaction where the C > CO > CO2 all 
at the surface below the pot. No real secondary and all the heat produced close 
to the same location. I would think that would require a narrow blast of air. 

 

Suggestion: Take a section of plastic pipe that holds about 4 Liters. Cap the 
top and bottom. The bottom cap has a ½” pipe fitted with a ball valve. The top 
cap has a ½” pipe coming out. That top pipe is connected to flex tubing and 
that connected to a stainless tube to draw in gas. Open the ball valve and set 
4L pipe in a water bath such that water enters and fills large pipe. Close 
valve and remove from water bath. Place the stainless tube at exact location 
you want to sample the gas (say under the pot). Open the ball valve to let the 
water drain and gas is drawn into the large pipe. The rate and volume is the 
same as the water draining. Leave a couple inches of water in the large pipe 
and close the ball valve. Shake to mix the gases. Place large pipe into the 
water bath, open the valve, so water filling and the stove gas exits the top 
where you can measure it using your tester. You might add a small amount of 
acid to the water to keep the CO2 from dissolving. Or add a known amount of 
NaOH to capture the CO2 (CO?) for analysis leaving the other gases for the 
tester.  With this setup a lot of the variables are controlled like air flow 
and temperature. You get an average or set your tester just below the input to 
get real time. 

 

Regards

 

Frank

 

 

Frank Shields

Control Laboratories; Inc.

42 Hangar Way

Watsonville, CA  95076

(831) 724-5422 tel

(831) 724-3188 fax

[email protected]

www.controllabs.com

 

 

 

 

From: Stoves [mailto:[email protected]] On Behalf Of 
Saastamoinen Jaakko
Sent: Wednesday, September 18, 2013 2:37 AM
To: Discussion of biomass cooking stoves
Subject: Re: [Stoves] Charcoal stove design

 

Dear Frank and Crispin,

 

the main DIRECT product in the reaction of carbon with oxygen is CO but also 
some CO2 is directly formed. CO that is formed can be oxidized to CO2 
(CO+½O2=CO2) at high enough temperatures in the vicinity of carbon particle or 
in later stage in the gas flow. So there are different zones along the gas flow 
in carbon particle layer when air (or gas) is flowing upwards through it: 

 

I)                Zone where exothermic reaction C+½O2=CO takes place (but some 
CO2 is also formed). Here the gas temperature is rather low because it is close 
to the inlet and the gas has not heated up enough. So CO is not burning well.  

II)              Zone where the gas temperature becomes high enough so that 
also the exothermic reaction CO+½O2 =CO2 (enhanced by H2O) takes place in the 
gas. This leads to even higher local temperature along the gas flow so that 
exothermic reactions (C+½O2=CO and CO+½O2=CO2) take place at even higher rate. 
Here also the endothermic reaction CO2+C=2CO takes place because the char 
temperature is high enough. This rrwaction adjust the temperature level 
preventing it to increase very high. Then at the location, where all oxygen is 
consumed, the gas temperature and CO2 concentration reach the maximum values.  

III)            After that the carbon reacts with CO2 producing carbon monoxide 
in endothermic gasification reaction CO2+C=2CO. The gas is cooled due to this 
endothermic reaction. If the layer is very thick, the gas is cooled to a 
temperature at which the reaction rate C+CO2=2CO becomes very low.

 

So some conclusions:

 

1.     For a thin layer, there is only zone I producing CO. 

2.     For thicker layer (zone II), the exit gas contains much CO2 and some CO. 
The exit gas is hot and CO may be burned introducing (preheated) secondary air. 
The exit gas is hottest if the thickness of the layer is just in the  
intermediate transfer regime from zone II to III. 

3.     For a thick layer, the gas contains much CO and some CO2. Its 
temperature is low and it is difficult to burn CO without highly preheated 
secondary air.

 

The reaction CO+½O2=CO2 can take place also in the other direction. This 
reverse reaction (dissociation) of carbon dioxide is not significant at 
temperatures <1800 K.

 

Regards 

 

Jaakko

 

From: Stoves [mailto:[email protected]] On Behalf Of 
Frank Shields
Sent: 18. syyskuuta 2013 0:55
To: 'Discussion of biomass cooking stoves'
Subject: Re: [Stoves] Charcoal stove design

 

Dear Crispin,

 

So the CO2 > CO is endothermic. But still needs carbon. As I see it the only 
difference is the temperature changing as the gases move around the pot. 
Wondering if the reading could be affected by temperature? Perhaps amount of 
gas entering the instrument or something? Interesting. Could hydrogen react 
with one of the oxygen in CO2 making water leaving CO?  

 

Frank

 

From: Stoves [mailto:[email protected]] On Behalf Of 
Crispin Pemberton-Pigott
Sent: Tuesday, September 17, 2013 2:01 PM
To: 'Discussion of biomass cooking stoves'
Subject: Re: [Stoves] Charcoal stove design

 

My conclusion is the CO splits endothermically. It does not happen in stoves 
with high EA.

Crispin

 

 

 

Dear Crispin,

 

<snip>

 

I found that directly above the middle of a good stove (under the pot) there is 
zero CO – I was amazed. But nearer the edges there is more.

 

[Frank >] How is that possible? I thought going from CO2 > CO could only occur 
be in a bed of char. This is very strange. 

 

Regards

 

Frank





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