Hi Doug & list,

I have moved the discussion to a more appropriate message header that better reflects the content. Also the messages so far skip across a lot of ground and it is too easy to get confused trying to cover multiple threads of discussion within one reply, more so when there is no differentiation in the text style between individual contributors.

In this message I will only focus on the gas out of the RPS linear hearth, it is already long winded but am attempting to provide as much detail as possible without compromising proprietary bits.

Doug has mentioned our gas analysis as being "very unusual" for an air drawn system so for the benefit of the list I provide it here so people can see for themselves:

Major Gasses,
Hydrogen: approx  36.00%
Carbon Monoxide : approx  28.00%
Nitrogen:    29.00%
Carbon Dioxide:      6.81%
Low level Gasses,
Oxygen:         Less than 0.02%
Methane:     0.96%
Argon:     0.37%
There were also a range of minor gases in the less than 50ppm range.

The flow rate measured at the time of the test was 130m3/hr, though this was not recorded on the lab certificate.

This is not full flow and the same system has been measured up to 400m3/hr without apparent over aspiration for a 20 minute run before overheating of the fan motor caused it to trip. The sustained upper limit has not been determined and may well be lower or higher (it has taken a while to get a suitable high temperature fan of adequate capacity, but will have one within the next few weeks, like most components we have ended up building this ourselves), but the system is quite comfortable at 200m3/hr with similar gas quality observed in the flare and can be turned back to 40m3/hr without losing this.

Now at this point of our development we are not making any loud noises about this, other than simply reporting it in a couple of local industry presentations and now here. Up until recently it was only a single analysis result. Instead we have largely kept our heads down and tried within our own limited financial resources understand what is happening, identify the feed stock parameters involved and get it further validated when we could.

We have made numerous attempts to engage university researchers to formally measure system performance without any real success. We had enormous difficulties in early days trying to get gas analysis done, with some amusing moments, like delivering a 4 litre gas sample bag of raw unfiltered gas taken hot from our development unit to the chemistry department of a local university because they indicated they could analyse it, then getting an excited phone call rattling off a long list of compounds they found, none of which included hydrogen or carbon monoxide gas... It turned out that they had released the gas and opened the bag to scrape a tiny amount of condensate from the inner sidewalls...and ran the analysis on this. The (uncertified) condensate analysis provided to us is nonetheless interesting and is copied below:

Condensate test results RPS first development unit

Percentage    Compound
40.625    Pyridine    C5H5N
2.298    Column Bleed
7.509    Phenol    C6H6O1
0.750    Methyl Phenol    C7H5O1
1.305    Methyl Phenol    C7H5O1

3.340    Naphthalene    C10H3
0.529    Dodlecene    C12H24
1.163    1 Methyl Naphthalene    C11H10
1.097    2 Methyl Naphthelene    C11H18
0.566    Tetradecine    C14H28
5.092    Biphenylene    C12H8
0.562    2, 3 Dimethyl 1 Naphthelene    C12H12
0.869    Dibenzofuran    C12H8O1
0.674    ?
1.125    Fluorene    C13H10
0.818    ?
0.552    ?
9.291    Anthracene    C14H10
2.077    Anthracene    C14H10
0.777    Anthracene    C14H10
1.626    4HCyclopentaphenathracene    C15H10
0.806    1methylAnthracene    C15H12
0.951    2Pheny1Naphthalene    C16H12
6.725    Fluroanthene    C16H10
1.762    Pyrene    C16H10
7.112    Fluroanthene    C16H10
100.001

Doug also indicated that if we are only getting low overall condensate levels then the water is probably going out with the gas as steam, and ordinarily I would agree, except none of our observations of our linear system whilst operating on optimal fuels support this.

The condensate analysis above does not show any free water at all (we did query this at the time and asked whether this result was after water had been excluded, ie reporting only the percentages of the non water component, but were told no, if water had been present it would have been reported).

Before I go on I would add that yes we have seen wet gas out of the system, but only when running truly excessively high mc feed stocks in the range of 30-50%. At 40% mc H2 drops to as little as 5% and CO to 11% with a corresponding increase in CO2 & N2 (lab analysis result during testing of mixed wood chip/ sewerage sludge blends). Stretching a length of paper towel over the (un-ignited!) gas stream under these conditions results in it getting rather damp quite quickly, and a brown condensate dripping off the outer rim of the flare head can be observed (no funny comments about the possible relationship to sewerage sludge please...). Under other much less extreme gasification conditions though no moisture collecting in the paper or free liquids on nearby metal surfaces are readily apparent.

The following additional observations are for "chunky" wood fuels below 25% mc (the fuel spec at the time of the formal gas analysis, piece sizes ranging from 25mm to 50mm on a side).

* Yes we do have gas cooling (of our own design like the rest of it), and gas exit temperature immediately prior to the flare head are between 40oC and 70oC, depending on flow rate, and the current system also includes mesh mist filters on the exit from the coolers, which we thought might also be an efficient way of trapping the sub 10 micron particulates, assuming that these would be wetted by condensate. You would therefore expect to see a higher level of condensate than we are getting, and I would have thought at least some steam visible in the plume on contact with cold air (we have run it at 0oC air temperatures in the middle of Winter without seeing such a plume).

*The formal gas analysis is consistent with a gas where a high proportion of the available moisture in the feed stock is being cracked.

* The system "chuffs" when the mc is below 25%, a resonance coming from the intakes sounding a little like a fast revving steam engine and the upper hopper vibrating like a long, low drum roll.... Hand held digital anemometer also records this as a regular, fast pulsing of the air intake flows.

This seems consistent with a rapid cycling of water cracking and the free oxygen made available displacing that from the incoming air. This cracking uses up thermal energy which then drops below the threshold required to support this water shift reaction, and the process pauses, reverting to pulling in outside air to satisfy the oxygen demand, temperature rises again and the process repeats. This has an immediate knock on affect as for each air derived oxygen molecule displaced then 4 nitrogen molecules don't make it into the system, lowering dilution from this source and raising overall gas quality.

* The reported gas quality is roughly mid way between a conventional down draft and a indirect pyrolysis system, which tends to support the above hypothesis as internal conditions cycle between air supported combustion and thermal mass as the gasification heat source. The big difference being the methane content, again consistent with more oxygen being available in the air drawn system, the preferred reaction then being Carbon + Oxygen, rather than Carbon + 4H2.

* We have seen a similar result when adding high oxygen content fuels such as glycerine (a triple alcohol group) to the wood chip feed, the flare quality and volume was maintained even though intake air flow rates dropped to <25% of their normal range!

*Simple mass balances taking into account gas flow rate (intakes and exit pipe), reported gas quality and measured fuel inputs closely agree.

*Charcoal from the ash bin has a very high fixed carbon in the 85-93% range (reported by a NATA certified lab) consistent with high temperature. Soot taken from the particulate collection system below the cyclones has been examined with a microscope and we are told it had a crystalline structure normally also only found when forming under high (>1000oC) temperatures.

My wife Kerry, equal co developer, has asked that I also point out when we designed the original system we made allowance for running it in either downdraft, or updraft, mode and have used this facility to break up bridging on occasion when working with difficult fuels (though on the early units this does interrupt the gas flow to the flare). The current (Mark 3.2?) under construction allows for this without stalling the system. This was done as part of improving the overall material handling side on the path to a more easily automated commercial model.


Cheers,
Peter




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