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A clean, efficient system for producing Charcoal, Heat and Power (CHaP)
C. Syred a,*, A.J. Griffiths a, N. Syred a, D. Beedie b, D. James c
a
Cardiff School of Engineering, Cardiff University, Queens Buildings, The Parade, Newport Road, Cardiff CF24 0YF, UK
b
BioEnergy Devices, Unit 28, St Theodores Way, Brynmenyn Industrial Estate, Bridgend CF32 9TZ, UK
c
James Engineering Turbines Ltd, 5 St Johns Road, Clevedon, Somerset BS21 7TG, UK
Received 13 March 2005; received in revised form 12 October 2005; accepted 26 October 2005
Available online 5 December 2005
Abstract
There is a strong domestic and industrial market for charcoal in the UK and is still used in many developing countries for cooking and heating as
well as for many industrial applications. It is usually made in small-scale simple kilns that are very damaging to the environment, very inefficient
and labour intensive. The Charcoal, Heat and Power (CHaP) process offers a method for producing clean efficient charcoal under pressurised
conditions and uses the product gas from the carbonisation process to drive a small gas turbine to produce heat and power. The charcoal is
produced using waste forestry matter and other waste wood, including that from sustainably managed forests. The CHaP system can also be used
in developing countries where there is an excess of forestry waste and a shortage of fossil fuels.
The CHaP process was initially designed, developed and a prototype system built. This paper discusses the CHaP design and the various
components used, their separate development and integration into a system. Tests showed the process successfully produced a high quality
charcoal and the product gas effectively used to drive a gas turbine. The CHaP technology was proven and a new novel system of producing
charcoal under pressurised conditions was created coupled with a novel use of the product gas whose output was green heat and power. The initial
CHaP prototype showed the process was capable of producing low emissions and is virtually carbon neutral.
q 2005 Elsevier Ltd. All rights reserved.
the wood being burned to ashes, a process which would take Charcoal in Europe is mainly used for the barbeque market,
around 10 days. During this carbonisation process, the pile although there are many other uses and the UK imports over
would contract in size as the volatile matter was lost from the 90% of its requirements. Interest is also growing in charcoal
wood. Average yield of charcoal from this type of kiln was as a renewable fuel. Developing countries and those short of
around 3540 bushels of charcoal per chord of original wood fossil fuels however, use charcoal as their main cooking fuel
(i.e. around 3545% of the original volume) depending on as well as for many industrial processes, such as smelting and
operating conditions and wood-type. One major disadvantage steel refining. Charcoal can also be activated by further
with this method of charcoal production was that a percentage refining and in this form is used in filters for water and air.
of the feedstock was burned to produce heat in order to power Charcoal can be used for medical purposes, both internally
the carbonisation process [1]. and externally. It is used in sugar refining, agriculture,
horticulture, and as an ingredient in animal foodstuffs.
2. Charcoal production developments Specific charcoals (i.e. those resulting from particular wood
species) are used for gunpowder and fuse powders, and also
Improvements to the traditional forest or pit kilns involved for artist charcoal.
building more permanent structures with bricks and more The Charcoal, Heat and Power (CHaP) process discussed in
recently, metal. This, however, presented the problem of this paper offers a cheap, clean and efficient method of
transporting large amounts of wood from the forest where it producing charcoal with the waste energy being utilised in the
was felled to the site of the carbonising facility. Initially, the production of heat and power. This process can be used in
first development was to replace the forest kiln with a very many situations both nationally and internationally. In the UK
similar structure built with brick bases, in order that the tar and the CHaP system could be used at forest management sites,
pyroglineous acid could be collected in pits and put to further also with traditional and urban forestry. The completed system
use. Later, domed brick kilns were built, which were uses wood sustainably derived either from urban forestry
themselves replaced with cast-iron retorts, where the wood to highway, amenity and domestic tree management operations
be carbonised was held in a cylinder separate to the fuel used to or from revitalised deciduous woodlands. It could, if required,
provide heat for the process. In this system, a brick-built utilise wood-chips from energy plantations or waste from
chamber incorporating a firebox remained hot while the cast- conventional forestry. In developing countries, the CHaP
iron cylinder holding the wood could be rapidly replaced, system could with modifications, use a range of different
saving time and heat energy. Quite a number of different biofuel and biomass materials. With increasing concerns over
designs were produced using this basic design principle, with climate change and the UKs commitment to increasing green
additions for collecting the tar, acid and wood-gas by-products energy, reducing CO2 emissions, the process can make a useful
of the process. contribution to sustainability. The process can also use a
During the late 19th and the 20th century, much larger sawdust fed gasifier to provide heat to feed the carbonisation
industrial plants were built for larger quantities of charcoal to process of the lumpwood. The hot gas (volatiles, tar, etc.)
be produced. Here, the wood and the final charcoal products driven off from the wood, combined with the gasifier gas, is
were held in railway-style wagons, which were pushed on then fed into a combustor. This combustor then fires a small gas
tracks into cast-iron tunnel retorts, and pulled out at the far side turbine to produce green heat and power. The whole system is
when the process was complete. In some designs, the gases operated under pressure. The CHaP system is thus an attempt to
produced by the carbonising wood were burned directly in the improve the efficiency of the charcoal manufacturing process
furnace, reducing the fuel requirements of the system. A large by utilising available energy to generate electricity and heat
system was developed for refining and treating the by-products efficiently and economically whilst also reducing emissions.
of the carbonising process, similar in form to the plant used The original system had a number of features in order to
today for refining oil. A number of large charcoal producing achieve these aims:
plants were built, incorporating both retorts and refinery
processes, enabling both charcoal and many other products to 1. As the carbonisation of wood is a cyclic process, a
be produced, thus providing the raw materials for a wide range modulated source of heat is required that can serve to
of other processes [2,3]. preheat the carbonisation vessel. This must be a gasifier to
Modern charcoal production methods have changed little avoid direct combustion of the lump wood intended for
from the traditional forest kiln and remain inefficient, time charcoal production in the carboniser vessel. This can be
consuming and environmentally unfriendly with over 60% of provided either by an available design of cyclonic gasifier
process energy loss. An extensive literature review found that for sawdust or bio-oil. This means that none of the
although some advances in charcoal production had been feedstock intended for charcoal production is burned for
made in the last century involving multiple batch loads, new heat generation, whilst the evolved low calorific value fuel
kiln designs, etc., these processes still remain inefficient and gas can be blended with those from the gasifier and fed to a
time consuming. These modified processes are now no longer special design of combustor. The combustor is used to fire
used and UK production of charcoal has reverted back to the small gas turbine, thus the polluting gases resulting from
more traditional kiln methods. Few references could be found the carbonisation process will be burned cleanly and used to
to work on charcoal production under pressurised conditions. produce heat and power.
1568 C. Syred et al. / Fuel 85 (2006) 15661578
2. The vessel for carbonising the wood will be operated at French and Belgium standards define the sizes of charcoal
moderate (gas turbine) pressures (3.2 bar absolute for the pieces that can be sold to the public: the French quote 85% to
pilot unit), higher pressures are envisaged later. be in the 20120 mm range and Belgium quotes a maximum of
3. As the small robust gas turbine is direct fired to avoid 10% below 20 mm and none over 160 mm. In Britain,
expensive gas cleanup systems, a special combustor had to generally, charcoal is sold in pieces between 20 and 80 mm
be evolved to deal with the variable mix of medium to low in size at time of packing.
calorific gases (LCV) from the carboniser and gasifier. This Proximate analysis results of a range of charcoal products
incorporated novel vortex collector pockets (VCPs) to resulting from a number of woods, as manufactured by
remove and collect ash particles down to 5 mm without the traditional processes are shown in Table 1 [4]. Most charcoals
need for additional cyclone collectors in the system. have a carbon content greater than 65% (with the exception of
the soft-burned sample) and a volatile matter content less than
This paper describes the origins of charcoal use and 26% (again, with the exception of the soft-burned sample).
production, and the techniques for producing it. As CHaP Moisture content is generally below 8% and typically ash is
uses a pressurised system, results from the available literature below 3% (although some exceptions exist). Moisture present
on the effects of temperature and pressure on the production of in the charcoal reduces the calorific or heating value of the
charcoal are also discussed. The CHaP system, a clean, charcoal, since energy is required to heat and evaporate the
efficient system for the production of charcoal, heat and power moisture.
is then described and a detailed discussion of the results from a For comparison, Table 2 shows the characteristics
prototype system made. demanded by a steel blast furnace plant in Brazil using
charcoal as a fuel. The table shows the range and yearly
3. Charcoal quality standards averages of the charcoal used. The charcoal is a mixture of 40%
eucalyptus charcoal produced in company kilns and 60%
Few standards exist which define the quality of charcoal, heterogenous natural wood charcoal manufactured by privately
particularly for the domestic market. Large industrial users operated kilns. The charcoal considered to be good to
have a much tighter specification for the charcoal they can use, excellent is that produced from eucalyptus wood in company
particularly in the metal industry. In the domestic (barbeque) kilns.
market, no British standard exists whilst in Europe standards
exist in Germany, Belgium and France, i.e. the German DIN 4. A qualitative description of the carbonisation process
51749, the French EP 846E and the Belgian NBN M11-001,
respectively. The German standard is quite specific on fixed The process of charcoal manufacture is known as the
carbon content, giving a minimum of 78%, and quoting destructive distillation of wood, and essentially involves
maximum percentages of volatiles, ash and moisture. The heating the wood to a temperature beyond 270 8C in an
Table 1
Typical charcoal [4]
Wood species Production Moisture Ash (%) Volatile Fixed Bulk density Bulk density Gross calorific Remarks
method content (%) matter carbon (%) (raw) (pulverised) value (oven dry
(m.c./%) (kg/m3) (kg/m3) basis) (kJ/kg)
Dakama Earth pit 7.5 1.4 16.9 74.2 314 708 32,410 Pulverised fuel for
rotary kilns (1)
Wallaba Earth pit 6.9 1.3 14.7 77.1 261 261 35,580 Pulverised fuel for
rotary kilns (1)
Kautaballi Earth pit 6.6 3.0 24.8 65.6 290 290 29,990 Pulverised fuel for
rotary kilns (1)
Mixed tropical Earth pit 5.4 8.9 17.1 68.6 Low grade char-
hardwood coal fines (1)
Mixed tropical Earth pit 5.4 1.2 23.6 69.8 Domestic charcoal
hardwood (1)
Wallaba Earth 5.9 1.3 8.5 84.2 Well-burned
mound sample (1)
Wallaba Earth 5.8 0.7 46.0 47.6 Soft-burned
mound sample (1)
Oak Portable 3.5 2.1 13.3 81.1 32 500 (2)
steel kiln
Coconut shells Portable 4.0 1.5 13.5 83.0 30 140 (4)
steel kiln
Eucalyptus Retort 5.1 2.6 25.8 66.8 (3)
saligna
Table 2 (vi) Temperature rises from 290 to 400 8C: Further break-
Characteristics of charcoal for a Brazilian blast furnace [4] down of the wood allows a number of gases to be
Chemical and physical Max Min Yearly Charcoal released such as carbon monoxide, carbon dioxide,
composition of charcoal average considered hydrogen and methane, in addition to condensable
(dry basis) (by weight) good to vapours such as water, acetic acid, methanol, and
excellent
acetone. Wood tars begin to predominate as the
Carbon (%) 80 60 70 7580 temperature rises further.
Ash (%) 10 3 5 34
(vii) Temperature levels around 400600 8C: The main
Volatile matter (%) 26 15 25 2025
Bulk densityas received 330 200 260 250300 process of carbonisation is complete, and the charcoal
(kg/m3) is known as soft-burned. This type of charcoal can
Bulk density (dry) (kg/m3) 270 180 235 230270 contain up to 30% weight of tar, trapped in the internal
Average sizeas received 60 10 35 2050 structure of the material. Further heating drives off
(mm)
more of the tar and increases the fixed carbon content of
Fines contentas 22 10 15 Max 10
received (!6.35 mm) (%) the final product.
Moisture contentas 25 5 10 Max 10
received (%)
6. The effects of temperature and pressure on the products
of carbonisation
oxygen-free environment. This breaks down the complex
cellulose and hemicellulose molecules mainly into H2O, CO, Some research studies provided experimental results
CO2, and char (solid carbon). The process of carbonisation is detailing the effects of temperature and pressure on the
generally described in terms of Primary reactions and gaseous and liquid products of carbonisation, and are shown
Secondary reactions. Primary reactions are conversions of in Fig. 1. Sadakata et al. [5] used mulberry wood in a
the basic wood constituents to products including gases, liquid laboratory scale experiment, rapidly heating the wood at over
tars and solid char, whereas secondary reactions reduce the 1000 8C minK1. Although the CHaP apparatus will not be
products of the primary reactions (in particular, the tars) to capable of heating the wood feedstock at this rate, their
lighter fractions and result mostly in gases. results provide some useful trends. Fig. 1(a) shows the
temperature effects of the decomposition products during
wood carbonisation. In general, the graph indicates that the
5. Temperaturetime characterisation
gas products increase while the solid char products decrease.
The fraction of condensed liquids and tars appear to decrease
The production can be typically described as a three-stage
slightly with increased temperature, although this seems only
process:
to have a significant effect when the temperature rises above
1. Drying the wood to expel all remaining moisture. 600 8C, above the operating temperature of the CHaP
2. Raising the temperature of the oven dry wood to 270 8C. At carboniser, and therefore beyond the scope of this project.
this point, the wood begins to decompose, and an Zaror and Pyle [6] collected data from a slow pyrolysis
endothermic reaction with spontaneous pyrolysis begins. process (in contrast to the results shown by Sadakata et al.
3. Final heating to 500600 8C to drive off tar and increase the [5]). Fig. 1(b) shows the effect of final pyrolysis temperature
fixed carbon content to an acceptable level. on charcoal yield. The graph suggests a decrease of solid
charcoal production with increasing temperature, with a
These three stages can be further refined into the following corresponding increase in the carbon content of the solid
five stages: fraction. This supports the results shown in Fig. 1(a) where
increasing temperature causes an increase in the gaseous
(i) Temperature rises from 20 to 110 8C: Wood absorbs products and therefore a corresponding decrease in the solid
heat energy, and releases water vapour. products. The gas emitted from the wood during carbonis-
(ii) Temperature will remain at or slightly above 100 8C ation (termed wood gas) is a mixture of a number of
until all moisture is driven off (bone dry). products. Fig. 1(c) shows the relationship between these
(iii) Temperature rises from 110 to 270 8C: Wood starts to component gases and process temperature. Fig. 1(d) shows
decompose, releasing some gases such as carbon the variation of the calorific value of the wood gas with
monoxide and carbon dioxide, and liquids, such as temperature, as given by two different sources [5,7] and
acetic acid and methanol. illustrates the range of wood gas calorific values that may be
(iv) Temperature rises from 270 to 290 8C: Endothermic expected at a specific temperature.
reaction commences in the wood. Antal et al. [8] used small amounts of biomass (w1 kg) in
(v) Temperatures remain above 270 8C. This allows the experiments to determine the effects of pressure on the
further breakdown of the wood to occur spontaneously, charcoal process. The design of the CHaP process requires
provided that the temperature of the wood is not cooled that the carbonisation vessel operates at an elevated pressure of
below 270 8C. 3 bar absolute, and these results provide an indication of
1570 C. Syred et al. / Fuel 85 (2006) 15661578
Fig. 1. Temperature effects on charcoal process [5,7]; (a) temperature effect on wood, (b) final pyrolysis temperature on charcoal yield, (c) component gas
relationship with temperature, and (d) calorific value of wood gas with varying temperatures
the likely effect of pressure on charcoal production. Fig. 2(a) different pressures on charcoal volatile matter, fixed carbon
shows a comparison of charcoal yield when operating a content and ash content respectively. Softwoods (Pine and
carbonisation system at pressures 1 and 10 bar. The results Spruce) showed a decrease in volatile matter, an increase
clearly show the charcoal yield is significantly increased with in fixed carbon content and an increase in ash content at the
pressure for all wood types. Fig. 2(b)(d) shows the effect of elevated pressure. Hardwoods (Alder and Oak) showed
Fig. 2. Effect of pressure on various wood species [8]; (a) charcoal yield, (b) volatile matter content, (c) fixed carbon content, and (d) ash content.
C. Syred et al. / Fuel 85 (2006) 15661578 1571
The combustor is an integral part of the CHaP system and emissions and good flame stabilisation are also necessary
must be capable of fully burning dual fuels, the LCV gas requirements of the system.
produced from the carbonisation and gasification processes and The next section of this paper describes the design and
a range of supporting fuels (initially oil). The combustor must development of the CHaP process and its main components.
have good heat storage capacity, produce low emissions and Initial tests performed on the system are also described.
fully burn out any tars remaining in the flow. Several studies
have been undertaken to develop LCV and dual fuel gas turbine 7.1. Carbonisation vessel and its ejector/flow recirculator
combustors. Problems encountered are numerous and include:
The Carboniser vessel and ejector recirculator was a main
Generation of non-premixed or diffusion flame to exclude
component of the CHaP system. The carbonisation vessel holds
the danger of flashback.
lump wood under pressure in a flow of hot oxygen-deficient gas
Maintaining high efficiencies whilst giving low NOx and
(generated separately by a gasifier). Hot gas is recirculated
CO. around the vessel by the use of an ejector and flow recirculator.
The necessity of using larger fuel nozzles and swirlers to As the hot gas passes over the wood, the pyrolysis process
handle the higher fuel gas volume. starts, volatiles are driven off, and charcoal forms. The volatiles
Issues of fuel quality restrictions such as hydrogen content, given off in this carbonisation process enrich the hot gas and
particulates, alkalis, heavy metals, tars, fuel gas tempera- raise its calorific value. Fig. 4 shows the design of the
ture, etc. carbonisation and recirculator vessel. A tenth scale prototype
The issue addressed in this paper are of redesigning the of the carboniser and ejector was initially built and isothermal
combustor to avoid any drop in efficiency by essentially and hot gas tests performed under atmospheric conditions with
increasing available residence time, whilst simultaneously conditions representative of those under pressurised con-
dealing with the contaminants in the LCV gas. ditions. The performance of the ejector was maximised by
testing isothermally and determining the optimum position of
There is a wide range of work in this area as discussed in the the nozzle in relation to the carbonisation vessel outlet port
literature [1217] where the issues raised above are more fully
discussed. These combustor designs are conventionally derived 900
from conventional gas turbine combustor systems fired on 800
conventional liquid fuels or natural gas. They are all designed 700
inlet
Temperature (C)
8. System analysis
The carboniser vessel was filled with wood and the CHaP
system was prepared for a full run. The gas turbine was
started by the auxiliary motor and then switched over to the
oil burner. The combustor was initially fired using the oil Fig. 10. RPM and oil flow with time.
burner to allow the combustors thermal mass to heat up.
After w12 min a steady combustor exit temperature was
9.8 MJ/kg. Emissions from the turbine were monitored
reached of 850 8C and a turbine inlet temperature of 720 8C.
throughout the tests. NOx levels remained at approximately
The turbine jet pipe exit temperature stabilised at 400 8C. At
80 ppm and could have been reduced by detailed attention to
this point the air valves from the compressor manifold to the
the secondary combustor. CO levels were generally low
gasifier burners air inlet was opened allowing the compres-
w10 ppm throughout the process except when the combustor
sors hot air (at w200 8C) to circulate around the carboniser
oil burner and gasifier oil burner was being ignited or
vessel and heat up the lump wood. The LCV gas inlet valve
to the combustor was then opened. The combustor exit and extinguished. This is due to large fluctuations in flame
turbine inlet temperatures then stabilised at 800 and 700 8C, temperatures and air to fuel ratios resulting in momentary
respectively. The jet pipe exit temperature remained constant incomplete combustion. As to be expected when the gasifier
at 400 8C. The system remained stable and the carboniser was switched on and off these levels rose to several hundred
inlet temperature increased to around 120 8C. After 35 min, parts per million, and gradually dropped back to a low level
the gasifier was turned on to provide heat to the carboniser once the system had restabilised.
vessel and the gasifier secondary air inlet opened. The Fig. 10 shows the turbine speed and combustor oil flow rate
gasifier was turned down and the air valves closed to the throughout the run. The turbine reaches it full speed after
gasifier and combustor. The lump wood slowly pyrolised and 2 min where it becomes stable. Throughout the run the turbine
a LCV gas given off. This gas was fed into the combustor speed was reasonably constant with small increases when
and burnt. A stable turbine inlet temperature was maintained gasifier was modulated. The oil flow rate to the combustor
by a control system that controlled the combustor oil inlet was monitored by a control system attached to the turbine.
flow. As more LCV gas entered the combustor the combustor This was controlled by the turbine inlet temperature. As LCV
oil burner flow rate was decreased automatically. A stable wood gas was introduced into the combustor the oil flow rate
combustor exit temperature and turbine inlet temperature of drops to maintain similar exit conditions, this is seen from the
820 and 700 8C, respectively, was maintained. The combus- fluctuations in oil flow rate in Fig. 10. Fig. 11 shows
tor oil burner flow rate was turned down from a full load of temperatures in the CHaP cycle whilst running. The
10.51.5 g/s when the LCV gas was at its maximum safe compressor exit temperatures remain reasonably constant
output. The output from the carboniser was maintained at a (w200 8C) throughout the run. The temperatures of the
stable rate by controlling the gasifier. To control the system combustor products from the oil fired burner at inlet to the
the gasifier needed to be switched on and off several times main combustor was varied across the run (average 1350 8C)
throughout the cycle to achieve steady carbonisation and
control the amount of LCV gas produced to maintain stable
combustor conditions. After typically 3 h and 40 min, the
system was turned down when no further gas was produced
from the carboniser. This corresponded to previous calcu-
lations as to the length of the carbonisation process. (The
system is a batch process and for commercialisation a second
carboniser would be used with a switch over valve,
maintaining continuous turbine use.) The carboniser was
opened and examined, charcoal had been produced.
Proximate analysis of the charcoal was performed, and
showed the process made a high quality product.
The lump wood was weighed before and after carbonis-
ation and gave a yield of 38%. Overall mass balance results
from the various fuels used in the system showed the wood
produced a gas giving a calorific value of approximately Fig. 11. Temperatures in CHaP cycle.
C. Syred et al. / Fuel 85 (2006) 15661578 1577
11. Conclusions
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