Furnace Design and Combustion Control to Reduce Emissions and
Transcription
Furnace Design and Combustion Control to Reduce Emissions and
EF Nr. 194010 Bundesamt für Energie Office fdraI de I‘önergie Ufficio federale deII‘energia Ufflzi federal d‘enerqia Biomass Programme Furnace Design and Combustion Control to Reduce Emissions and Avoid Ash Siagging International Energy Agency, Biomass Combustion Activity 1997 Final Report of the Triennium 1995 — Thomas Nussbaumer Swiss Federal Institute of Technology (ETH), CH Verenum Research, Langmauerstrasse 109, CH SWITZERLAND — — 8092 Zürich and 8006 Zürich on behalf of the Swiss Federal Office of Energy March 1998 Final Report Contents 1 Summary .5 2 Introduction 6 2.1 Motivation 6 2.2 Objectives 6 2.3 Definitions 7 3 IEA Contributions 3.1 Experiments on a moving grate furnace in Switzerland 8 8 3.2 Experiments for the investigation of ash cieposition in USA 10 3.3 Experiments with a whole bale furnace in Denmark 11 4 Fuel Chararcteristics of Biomass 1 2 4.1 Composition of biomass 12 4.2 Triangular diagram combustible—water—ash 14 4.3 Nitrogen content in the 1 uel 15 4.4 Content of sulfur, chiorine and potassium in the fueE 15 5 Furnace Design and Process Control 1 7 5.1 Fundamentals of biomass combustion 17 5.2 Automatic wood furnaces 20 5.3 Furnaces for herbaceous fuels 22 5.4 Process control 23 6 Emissions and Depositions 26 6.1 Nitric oxide emissions 26 6.2 Particle emissions 27 6.3 Particle Separation in a rotating particle separator 29 6.4 Chlorine emissions 31 6.5 Deposit formation 32 6.6 Dioxins and furans 34 7 Reterences 35 1 Summary The aim of the present project was to describe the main influences of the fuel characteristics, the furnace design, and the Operation conditions on the formation of emissions during biomass com bustion. Furthermore the parameters which can cause ash slagging and which influence the formation of depositions should be identified. The relevant parameters were investigated in different projects within the framework of the IEA Biomass Combustion Activity. Detailed results from different research projects have been contributed 1 rom the Swiss Federal Institute of Technology and Verenum Research from SWITZERLAND and from Sandia National Laboratories from USA. Furthermore several informations have been contributed from all other IEA members during the IEA seminars and project meetings from 1995 to 1997. The present study gives an overview on typical fuel characteristics of wood and herbaceous fuels such as straw, miscanthus and herbage-grass (hay). lt is shown that herbaceous biomass has significantly higher contents of nitrogen, chlorine, potassium and ash. Furthermore the ash softening temperature 15 lower than tor native wood. The main process steps during combustion are described in the report and typical biomass furnaces are presented. lt is shown that the formation of unburnt pollutants (CC, HC, PAH) can be avoided by complete combustion. An appropriate furnace design is needed with agood mixing quality between combustion air and combustible gases. Advanced combustion control technologies can be applied to guarantee optimum combustion conditions in practice. NO emissions are formed from the fuel bound nitrogen. Therefore specitic measures in the com bustion process such as air staging or fuel staging are necessary to reduce NO formation. In the opposite to CO emissions, NO emissions cannot be reduced below a certain level by primary measures. To meet bw emission standards, secondary measures can be applied. Particles from biomass combustion are mainly in the aerosol range < 1 jim. To achieve 10w particle concentrations in the flue gas, fabric or electric filters are needed. As an alternative to filters, a rotational particle separator has been investigated which offers a better Separation efficiency than cyclones. If herbaceous fuels are burnt, significant concentrations of chlorine can be found in the fuel and in the flue gas. Most of the chlorine is emitted as salt (mainly as KCI) which can lead to depositions on the furnace walls and in the boiler. Due to the bw ash softening temperature of herbacous biomass, significant ash slagging can occur on the grate. Since there is a conflict between achieving a complete burnout (high temperature) and avoiding ash slagging (10w temperature), the furnace design and Operation tor such fuels is different from native wood. Special measures such as cooled walls in the grate section of the furnace and flue gas recirculation are considered for these fuels. 5 2 Introduction 2.1 Motivation The flue gas emissions and the combustion efficiency are influenced by the fuel characteristics, the furnace design and the operation conditions. For woody biomass, appropriate combustion techno— logies are available which ensure high combustion quality and high efficiency and which are able to guarantee Operation with 10w maintenance effort. The Operation fl practice can be optimized with an appropriate combustion control system. However, there are still furnaces available which do not consider the specific combustion characteristic of biomass sufficiently. Furthermore fuel specific pollutants as nitrogen oxides can be emitted also in furnaces with appropriate combustion design. Furthermore the combustion of biomass with 10w ash softening temperature like straw, grass, and miscanthus, ash slagging on the grate and ash depositions on the the furnace walls and in the boiler can cause severe Operation problems and damage the furnace. To reach a good combustion quality a high temperature in the combustion chamber is necessary, while 10w temperatures are needed to avoid slagging. Therefore a conflict between the requirements to reach 10w emissions and to avoid Operation problems can be found. 2.2 Objectives In the present project the main influences between furnace design, operation conditions, emissions, efficiency and ash behaviour are studied. Results from experiments and data from the literature are used to consolidate principles of furnace design and operation. For that purpose the influence of the following parameters on emissions, ash slagging and ash deposition have been investigated: • overall excess air ratio and resulting combustion temperature • influence of over- and under-stoichiometric conditions in the gasification zone (primary excess air ratio) • quality of the primary air distribution in the gasification zone and of the homogenousity of the fuel bed (avoiding wholes in the fuel bed with continuous movement of the grate) • cooling of the furnace walls and cooling of the grate and • flow direction of fuel and gas in grate furnaces (co-, cross- and counter-current). 6 2.3 Definitions During the thermal treatment of biomass in the furnace, the processes of drying, pyrolysis, gasification and oxidation take place. To define the different process steps of thermochmical conversion, the ratio of fuel to air is described by the excess air ratio ? as follows: = rii, mVSh = amount of air supplied stoichiometric amount of air The characteristics of the different process steps can be described by the excess air ratio and the temperature as shown in Table 2.1. Process Excess air [—] Combustion > Gasification 0.2 Pyrolysis 0 Table 2.1 < < 1 Temperature [°C] 800 — 1 ‘300 Main product hot exhaust gas Most important applications of the main product Production of hot water, steam, and hot gas. Steam and hot gas for electric power prod uction. 0.5 700 — 900 producer gas of high thermal value Fuel tor gas engine, gas turbine, sythesis gas (e.g. as basis tor fuel or methane), and fuel cells (< 0.2) 400 — 700 liquid of high thermal value (pyrolysis oil) Fuel for diesel engine or gas turbine. Gas is used internally in the process, charcoal accumulates as a by-product. < Characterization of thermochemical conversion processes combustion, gasification, and pyrolysis. The excess air is the ratio of supplied to stoichiometric amount ot air needed tor a complete combustion. *For pure pyrolysis, 2 = 0. In reality a part of the conversion products gets burnt right away, therefore can also be slightly bigger than 0. 7 IEA Contributions 3 Different investigations on the described subject were carried out in Switzerland by ETH and Verenum which have been funded by the Swiss Federal 0ff ice of Energy as part of the biomass research programme. Furthermore the IEA members were asked to contribute with experimental data from combustion experiments in furnaces and laboratory equipment under varying conditions on emissions, ash siagging, deposition formation and deposition reduction. An important contribution to the present project came from Sandia National Laboratories (USA), which is involved in research on deposit formation in biomass fired boilers. Furthermore a research scientist from ETH was at Sandia during approx. 6 months to carry out specific combustion experiments on a plug flow laboratory reactor (Multi Fuel Combustor, MFC) which gave the opportunity to compare deposition formation found in grate furnaces in Switzerland with depositions found in biomass fired power stations in the USA and respective laboratory experiments in the MFC. The main experiments which contributed to the present project are described in the present sections. 3.1 Experiments on a moving grate furnace in Switzerland Combustion experiments have been carried out in Switzerland in cooperation with the furnace manufacturer SCHMID AG, Eschlikon: — Combustion tests with pellets and briquetts of grass (hay from extensively used land) and miscanthus in comparison to wood fuels. — — Monitoring of the main emissions (continously: CC, C0 , N0; particle concentration, particle size 2 distribution and further emissions (HCI, NH 3 ‚PCDD/F etc.) are measured discontinously) Temperature measurements are carried out at several locations at the grate and at the side walls to investigate the influence of the temperature an ash slagging Figure 3.1 Moving grate furnace with 450 kWth (SCHMID AG, Eschlikon, Switzerland) 8 — Mass flows of residues are determined and the composition of the residues are analysed and compared to regulations tor the use as tertilizers (bottom ash and cyclone ash) and for landtilling (filter ash). The experiments showed essentially the tollowing results. • Grass and miscanthus can be burnt with high combustion quality and 10w C0-emissions (< 1 00 3 at 11 Vol.-% 02). However severe Operation problems can be found with grass and mg/Nm miscanthus due to ash siagging on the grate, ash deposition at the side walls of the primary combustion chamber and depositions and fouling in the heat exchanger tubes. Ash siagging on the grate can be avoided with improved grate design and ash moving equipment. Furthermore lt is assumed that water-cooled walls in the primary combustion chamber are necessary to avoid depositions. However air-cooling of the side walls was not sufticient to avoid ash depositions. • For the heat exchanger tubes the injection of pressurized air or vapor tor a periodical cleaning can was succestully applied. However it the depositions exceed a certain temperature, agglomeration and condensation can lead to very strong depositions which cannot be removed by pressure shocks. Theretore the heat exchanger inlet temperature must be limitied. Investigations from USA (Baxter et al.) show, that tor superheaters a temperature > 850°C is critical while tor temperatures < 750°C no severe problems are tound. lt is assumed that the gas temperature in hot water heat exchangertubes may be higher due to lower wall temperatures than in superheaters. However no quantitative data are known. • If the energy is used tor space heating only, lower heat exchanger inlet temperature are not of relevance tor the etticiency. Theretore it is proposed that an efficient water cooling ot the primary combustion chamber, which leads to an energy output of approx. 50% ot the overall heat, can be applied. Furthermore flue gas recirculation can be applied as a measure to limit the temperature. However experiments so far were not satisfying since a large amount ot recycled tlue gas is necessary for an effective temperature reduction. Furthermore a test equipment has been built to carry out precipitation tests with ditterent types ot cloth filters under varying conditions (temperature, pressure drop, velocity etc.) and using ditterent additives tor the adsorption of HCI. To investigate the deposition formation, experiments were carried out in the grate turnace as weil as in a 100 kW under stoker. Placement of the deposit sampling probe Secondary air inlet holes Service doors Hearth with primary air inlet Figure 3.2 100 kWth underfeed stokerturnace (TIBA-MUELLER AG, Balsthai, Switzerland) 9 3.2 Experiments tor the investigation ot ash deposition in USA As an opportunity within the IEA Biomass Combustion Activity, a PhD student from Switzerland (H. Kaufmann) carried out a research visit at Sandia National Laboratories in Livermore (CA, USA) in the group of L. Baxter. The aim of the research visit was to start an improved exchange of experience and to carry out specific experiments with the biofuels used in tests in Switzerland at the mufti-fuel combustor equipment at Sandia. The multi-fuel combustor allows to carry out deposition experiments with different types of fuels, which are injected as small particies (coal, biomass etc.) or as gaseous fuels. The combustion conditions (temperature, excess air) can be varied and the exhaust gas is used at different temperatures to simulate ash deposition conditions as they are found in boilers. The deposition rate on a water cooled heat exchanger tube can be measured by an electronic balance. Furthermore the composition of the deposition can be analysed on-line with spectrometric methods (FTIR, laser-spectroscopy) and off-line, after a certain time of exposures, by analysing the composition of the depositions. Heatedf insulated modules Pcsv Laser beam to Exliaust Figure 3.3 Laboratory plug flow reactor (MFC) for at Sandia National Laboratories. Since many experiments of this type have been carried out at Sandia with direct exposure of the heat exchanger tubes in the exhaust gas, mainly two specific questions were investigated within the present project: 1. A comparison between grass combustion in grate furnaces and in the MFC 2. The difference between depositions with direct exposition of the heat exchanger tube in the flue gas and with a preliminary extraction of the arge particle. This objective is important for a comparison with depositions found in grate furnaces since an effective extraction of large particles on the grate can be achieved. 10 During the research visit of H. Kaufmann at Sandia, respective tests with grass from Switzerland have been carried out. The resuits are described in detail in [Kaufmann et al. 1998]. Figure 3.4 3.3 Arrangement of sampling cylinder A and protection cylinder B in the outlet of the MFC Experiments with a whole bale furnace in Denmark For the use of grass or miscanthus in grate furnaces the fuels must be transformed to pellets or briquetts. In the overall economy, the pellet fabrication is a relevant cost factor (costs in Switzerland app. CHF 110.—lt = ECU 70.—lt = USD 851t). Therefore the application of whole bales of grass as they are used in agriculture is a favourable Option. Straw boilers with whole bale furnaces are mainly in use in Denmark, where different types of furnaces and feeding systems have been developped. For large units (>2 while for smaller units (>200 kW — — 3 MWth) cigar burners are used, 2 MWth) special feeding Systems are used to cut the straw bales into slides and feed the furnace with one slide (app. 20 cm) of a bale. Since there are only few experiences with grass, combustion tests were carried out on a whole bale furnace with bale-cutter of app. 1.5 MWth using grass as it was used in the combustion tests in Switzer land. However the combustion tests were not succesfull due to unsufficient ignition of the grass in the primary combustion chamber. The manufacturer of the whole bale furnace assumes, that the primary combustion chamber has to be adopted by adding a radiation surface to increase the temperature. However an increase of the temperature in the primary combustion chamber can also lead to slagging and deposition problems which are not found in straw firings. Unfortunately it is not possible to answer the questions whether grass can be used in whole bale furnaces without slagging and deposition problems by the experiments carried out as a part of this project. Therefore further experiments for a comparison between straw and grass were carried out in the grate furnace in Switzerland. 11 4 4.1 Fuel Chararcteristics of Biomass Composition of biomass Table 2.1 shows the typicat composition of wood, grass, miscanthus and straw. The thermal value and the combustion properties are mainly dependent on the percentage of organic substance in the fuel. For biogenic fuel water and ash content are the most important parameters. Furthermore, the combustion characteristic is dependent on the physical properties as size and specific surface. Not only the percentage of ash is important, but also its melting properties. Wood ash has a much higher melting point than ash of grass, miscanthus and straw. The emissions of pollutants and the required measures to be taken are dependent on the content of nitrogen, sulfur, chiorine and potassium, which is much higher for grass, miscanthus and straw than 1cr wood. A correlation 01 the nitrogen content with the sum of potassium, chiorine and sulfur content can seen in Figure 4.4.It can also been seen, that the content of potassium, chlorine and sulfur is de creasing with increasing lignification and demineralisation. The content of potassium, chiorine and sulfur is in general higher in grass than in straw and higher in straw than in miscanthus. Phosphor and potassium content influence the content of nutrients in the residues. The content of lead, cadmium, chrome, cobalt, copper, molybdenium, nickel, mercury and zinc influence the amount of pollutants in the residues and the heavy metal emissions in the flue gas. For particle emissions of less than 1 50 3 significantly less than 2 mgINm mgINm 3 of lead and zinc and significantly less than 0.2 mg/Nm 3 of mercury can be reached. 12 U nt Wood Grass Miscanthus Straw Influence* Ash content medium [weight-%] 0,2 9,8 2,43 6,0 1 Ash contenttypical [weight-%] 0,1—1 6—12 1—4 4,5—7,5 1 Watercontent [weight-%] 10—60 5—20 5—20 5—20 1 ThermalvaIueH [MJ/kg , 1 j 18,5 16,8 17,9 17,5 1 Sinterbeginn [°C] 1180 870 840 830 1 Erweichungspunkt [°C] 1470 970 880 940 1 Haibkugelpunkt [°C] 1600 1040 1040 1100 1 Fliesspunkt [CJ 1640 1120 1100 1170 1 ** ** C [weight-%] 50 H [weight-%] 6 1 0 [weight-%] 44 1 N [weight-%] 0,08 1,90 0,58 0,54 2 S [weight-%] 0,01 0,20 0,08 0,14 2 Ci [weight-%] <0,001 0,44 0,15 0,37 2 K [weight-%] 0,11 2,45 0,47 1,20 1,2,3 Si [weight-%j 2,14 1,60 0,91 1 Ca [weight-%] 0,61 0,20 0,29 1, 3 P [ppm] 720 3 Pb [ppm] 1,1 0,7 2,5 0,5 3 Cd [ppm] <0,1 0,10 0,11 0,09 3 Cr [ppm] < 0,5 3 Co [ppm] <0,1 3 Cu [ppm] 1,9 7,6 2,9 2,9 3 Mo [ppm] <0,2 0,9 0,4 0,5 3 Ni [ppm} < Hg [ppm] Zn [ppm] Table 4.1 0,27 ** 1 1,2 3 11 0,01 0,01 0,02 3 38 21 7 3 Typical composition of wood, grass, mscanthus and straw. Data from [Hasler et al. 1996] and [Hofbauer 1994] * 1: Combustion technique, 2: flue gas cleaning, 3: residue quality The differences of C, H and 0 content in different tree species are small. According to Browning [1963] five different leaf and coniferius trees only show the following range: C of 48.9 to 50.2 weight-%, H of 5.8 to 6.1 weight -% and 0 of 43.4 to 44.5 weight -%. ** As the contents of C, H and 0 is only little different for different plants, the values for wood can be taken as an assumption for grass, miscanthus and straw. 13 4.2 Triangular diagram combustible—water—ash For a characterization of the fuel regarding the combustion properties, the percentage of combustible matter, the water content and the ash content are of importance. These fuel properties are shown in the triangular combustible—water—ash diagram. Furthermore the diagram allows to show the operational range of different combustion systems. Figure 4.1 shows the thangular diagram for native wood, bark and grass, miscanthus and straw. The combustion properties of wood and grass are significantly different. Grass has a high ash content but with the current fuel storrage and a 0w humidity (w < 20 weight-%). Native wood chips have a bw ash content but usually a higher humidity (w = 25% 55%). Berk has a medium ash content and a high humidity (up to 60%). Waste wood can have high or bw amount of ash or water, depending on its origin. Under stoker furnaces can be used tor wood with a 10w ash content and a bower or higher humidity. They usually reach up to 1 —2 MW. Different types of grate furnaces are mostly used tor wood woth a high ash content and a high water content, as they have a better ash removal and therefore a higher operational range. - Herbaceous fuels Grate furnace Native wood, bark Under stoker furnace 100 100 80 80 Ash [weight-%] ‘ 60 Water Ash Water [weight-%] [weight-%j [weight-%j 60 40 40 20 20 0 0 0 Figure 4.1 0 cP Combustible Combustible [weight-%] [weight-%] Triangular diagram combustible water ash [Biollaz and Nussbaumer 1996]. left hand side: compostion of the fuel (wood and grass) right hand side: operational range of under stoker and grate furnaces - - 14 4.3 Nitrogen content in the fuel Figure 4.2 shows the frequency distribution of nitrogen content in grass, miscanthus, straw and wood. The nitrogen content is increasing with an increasing protein content. The ranges of wood and miscanthus are comparable (wood: 0.05 0.65 weight-%; miscanthus: 0.06 0.87 weight-%). Straw has a significantly higher nitrogen content, which is in a fairly small range (0.4 1.0 weight-%). Grass, including hay for feeding, have the highes nitrogen content in a large range (0.7 4.9 weight-%). The treatment of the soil has a big influence on the nitrogen content of grass. As long as the soil is enriched with nutrients, the grass has a high nitrogen content. A decrease of the nitrogen content in the grass can only be expected after several years of extensive farming and after a decrease of the nutrients in the soil. — — — — 60 .Grass Miscanthus 50 0 S traw > 40 0 0 W ood 30 20 cl) 10 0 ii cJ-cDQcJj d d d o — — Figure 4.2 4.4 oc‘ CDO — — c‘J — c‘J CJ ‘N N-content [weight-%] C) C‘) 0 C‘) C) C‘) Frequency distribution of the nitrogen content of grass, miscanthus, straw and native wood. Content of sulfur, chiorine and potassium in the fuel The sulfur content is dependent on a few proteins of the plant and therefore only covers a small range.Chlorine and potassium are mainly assimilated as salts. Sulfur, chlorine and potassium from the fuel form salt (KCI, 4 S0 at the combustion. The sum of potassium, chtorine and sulfur is taken to get 2 K ) an indication on the amount of particies (safts) that are to expect. Figure 4.3 shows the frequency distribution of the sum of potassium, chlorine and sulfur of grass, miscanthus, straw and native wood. Compared to beech and coniferous trees, a higher content of K, Cl and S was found in fast growing trees as eucalyptus or poplar (0.04 0.43 weight-%). The content is continuously increasing from miscanthusto strawto grass (miscanthus: 0.11 1.1 weight-%, straw: 0.17 2.3 weight-%, grass 1.78 4.86 weight-%). Straw is a good example to show that these sdubstances are soluble in water. Straw for atraw furnaces in Denmark is divided in yellow straw (that has not been rained on) and grey straw — — — — 15 (that has been rained on). The grey and dry straw has better combustion properties and is therfore preffered for combustion. Younger plants have a higher content of substances being needed for their growth, as they have a higher number of cells still growing. Therefore a higher content of sulfur, chlorine and potassium can be found at higher nitrogen content (see Figure 4.4). 70 • Grass i Miscanthus Straw c Wood 60 > 50 0 40 c3G) 30 4- 20 cl) 10 0 ID C‘J 0 0 ID 0 ID 0 0 - — L LX) Lf) 0 0 ID-QC‘J CJ — CJ r—ocj 0 ID IDCJ CJ 0 ID 0 ID 0 OCLOC) C) c) c) ID 0 0CJLf) ID r— . 0 0 1 Content of K+CI÷S [Gew.-%] Figure 4.3 Frequency distribution of the sum of potassium, chlorine and sulfur for grass, miscanthus, straw and natve wood. 5.0 . . 4.0 •• •.:‚. . 3.0 — . . ••:. : > 2.0 A •%• • • •.• • •• • ••• •• •. •Grass ‚Miscanthus Straw 1.0 E (1) . . 0.0 0.0 1.0 2.0 3.0 4.0 N-content [weight-%] Figure 4.4 Correlation of nitrogen content and the sum of potassium, chlorine and sulfur tor grass, miscanthus and straw. 16 5 Furnace Design and Process Control 5.1 Fundamentals of biomass combustion The goal of combustion is to transform all of the chemical energy of wood into heat by oxidation. The combustion of wood consists of several steps. At first the wood is dried by the heat in the combustion chamber and decomposed to gases and charcoal by contact with the combustion gas. With the supply of air the charcoal is then gasified to carbon monoxide. The gasses emitted by the wood and the charcoal finally oxidize with the combustion gas in a gas flame. For electric power and heat production the hot flue gasses pass their energy on to a working medium in a heat exchanger, e.g. to water for producing steam. The heat can also be passed on to another gas in a hot gas heat exchanger. The heated gas can then be used in a Stirling engine or in a closed cyclic process to produce mechanical power. With modern combustion technology it is nowadays possible to get an almost complete combustion of the gases and thus an energy use that is poor in emissions. Wood (CHmOnNo) Primary air (2 <1) i. Gasification Combustible gases CO, H , 4 2 CH NH , , HCN, NO, etc. 1 Secondary air (2 < Oxidation 1) Flue gas C0 HO, NOx , 2 Figure 5.1 Two stage combustion of wood with primary air for gasification and secondary air for burn out of the combustible gases [Nussbaumer 1989]. 17 The combustion technology has little requirements to the fuel characteristics. The wood can be of different sizes, even with a high content of fine material, and it can contain up to 60% of humidity. Even impurities and contamination do not cause any problems, if the plant is professionally planned and realized. The combustion technology tor plants of 20 kW to 100 MW is tully developed. Good construction as weil as controlling and regulation of modern plants allows 10w emissions of unburnt pollutants (carbon monoxide, organic carbons) even at changing bad. Very efficient technobogies exist tor reducing nitrogen oxides, dust, and other pollutants resuiting from impurities in the wood, in the exhaust gases. The limits for the measures for reducing emission are primarily given by the investment and operating cost. The amount of emitted pollutants is very 10w if a reasonable effort is made in emission control. Especiaily dust and nitrogen oxide emissions are of importance. The additional cost of denitrification and dedusting at larger plants is economically acceptable. The ash of the combustion of uncontaminated wood can be used as a tertilizer. Residues from emission control have to be disposed of. Waste water from plants with exhaust condensation has to be treated before being fed into the sewage system. Co 0 1 2 3 4 [-.1 5 Excess air ratio Figure 5.2 Carbon monoxide emission as a function of the excess air ratio. a)simple manuallycharged log wood boiler b) downdraft boiler tor log wood c)automatic furnace with combustion technology (as of 1990) d) automatic furnace with enhanced combustion technology (as of 1995) Automatic furnaces with appropriate combustion control technique can be operated at Optimum conditions. 18 10 fl 9— %mNJ1 2 l2 3 8Ai 7— ‘.‘I ‘1 1 \ 1 4 ttt t 6— Figure 5.3 jI :ti (I1I t —5 Sectional view of a modern log wood boller with downdraft principe (TIBA, Bubendorf, SWITZERLAND). 1 3 5 8 Log wood storage, 2Drying zone Pyrolysis and gasification zone, T = 150 600°C, 4GIow bed, T = 800°C Primary air inlet, 6Secondary air inlet, 7 Oxidation zone, T = 600 1000°C Combustion chamber, 9Heat exchanger, 10 FIue gas exit, T = 180- 200°C - - 19 5.2 Automatic wood furnaces The most important designs for automatic wood furnaces can be distinguished as follows (Table 5.1): Performance range Type Fuel Water content (wet basis) Under stoker furnace 20 kW 2.5 MW Native wood chips, waste wood chips — 5% — 50% with a < 1% Moving grate furnace 150 kW — 100 MW All kinds of wood, also 5% — 60% wirha»1% Preoven with grate 20 kW — 1.5 MW Dry waste wood chips 8% — 35% also witha> 1% Bubbling fluidized bed furnace Circulatingfluidized bed furnace (CFB) Dust burner 5 MW— 15 MW d < 10 mm 5% 15MW—100MW d< lOmm 5%—60% 5 MW—10 MW d <5 mm usually < Dust burner in coal power plant total 100 MW— 1 GW Wood: d <2—4 mm Wood max. 10% Table 5.1 — 60% 20% usually <20% Overview of the most important designs of wood furnaces (a = ash content). Several types of automatic and manually fed biomass furnaces exist. The most common furnaces used tor wood chips are unders stoker and grate furnaces (Figure 5.4 and Figure 5.5). Under stoker furnaces are built from 20 kWth to 2 MWth and they are suited tor fuels with 10w ash content and water contents on wet basis up to approx. 50%. Moving grate furnaces are built from approx. 200 kWth to 20 MWth and they can be used for fuels with higher ash content and water contents up to approx. 55%—60%. Furthermore dust burners, bubbling fluidized bed and circulating fluidized bed furnaces are used for biomass combustion, especially for dry fuel which is grinded to small particle sizes. Due to high investment cost, these furnaces are applied for larger plants (Figure 5.6, Figure 5.7, Figure 5.8 and Figure 5.9). 20 Figure 5.4 Under stoker furnace: 1 fuel supply, 2 hearth, 3 primary air inlet, 4 secondary air inlet, 5 combustion chamber, 6 heat exchanger, 7 insulation, 8 cyclone, 9 ash discharge. Figure 5.5 Grate furnace: 1 fuel supply, 2 grate, 3 primary air inlet, 4 secondary air inlet, 5 combustion chamber, 6 heat exchanger, 7 insulation, 8 cyclone, 9 ash discharge. L Brennstoff Figure 5.6 Dust burner tor fine wood particies. Figure 5.7 Bubbling fluidized bed combustor. Gas. 1.... Gas L45 FJ[ FUeI A[ FIXED BED BUBBLING CIRCULATING /t LOI (-p) LOG (veloclty) Figure 5.8 Principle of fixed and fluidized bed. Figure 5.9 Circulating fluidized bed combustor. 21 5.3 Furnaces for herbaceous fuels Hearbaceous fuel requires different fuel supply Systems than wood, especially straw. Straw Is mainly used in Denmark, where lt is pressed into rectangular bales at the harvest. The straw bales can be burnt as a whole, corresponding to a manually fed log wood boiler in its combustion properties. The alter natives for a controlled combustion would be a cigar burner (see Figure 5.10) which is pushing the whole bales the way that only their front face is burning or a turnace with bale cutter (see Figure 5.11), that always cuts a part of the bale and continuously pushes lt on the grate. A good continuous combustion, even tor smaller performances, can be achieved with this kind of furnace. Figure 5.10 Cigar bumertor straw bales Figure 5.11 Bale furnace with bale cutter (Linka) The storage and the combustion of bales requires a specialized technology and logistic. The energy density of bales is much less compared to wood chips and therefore the technology requires much more space. An alternative to the combustion ot bales are pellets of herbaceous tuels. Pellets have a higher energy density and can be used in moveing grate furnaces, as the handling is much easier. Due to the high content in ash and to the high risk ot siagging, turnaces tor herbaceous tuels have a cooled combustion chamber and a powerfull ash discharge system. Furthermore, measures to prevent depostition or tor automatic cleaning have to be taken. 22 5.4 Process control Elf iciency improvement for combustion processes demands bw fluegas temperature and bw oxygen content. In biomass combustion, the amount of unburnt pollutants, i.e. CC, HC, PAH and soot, is highly influenced by the excess air ratio. At excess air ratios below a certain Optimum value, the unburnt pollutants rapidly increase by a factor of 10 or 100. With increasing excess air ratio above an optimal value, the amount of unburnt pollutants slowly increases (see Figure 5.1 and Figure 5.3). Control technique on biomass furnaces has progressed very much since the last ten years. While the first gen eration of automatic wood furnaces were operating only at nominal heat output, the next generation could also run at 50% 01 the nominal heat output. The standby hours were again remarkably reduced by bad control technique being able to vary the heat output between 30% and 100% of the nominal heat output. To operate at high efficiency and 10w emissions, an aciequate combination of bad and combustion control technique was necessary [Nussbaumer 1989, Good 1992]. The most important combustion control techniques used in combination with bad controb are control of the temperature in the combustion chamber (flame temperature control) and control of the excess air ratio (lambda control). These control techniques dont use any information about the actual amount of unburnt pollutants and therefore the settings of the combustion control techniques used today are usually conservative, i.e. the setpoint tor the excess air ratio is rather high to avoid incomplete com bustion. The Optimum excess air ratio is influenced by the furnace design and the operating conditions, such as heat demand and fuel properties (humidity, specific weight). Experiments showed, that the correlation between CO emissions and excess air ratio shifts to higher excess air with decreasing heat output or with increasing fuel humidity (Figure 5.1). Therefore selftuning setpoint opti mization algorithms were developed to find the optimum excess air ratio for different furnace desings and changing operating conditions. 100000 ] 3 [mg/m lower heat output and/or higher tue! humidity 10000 co x:_« 1000 100 range 01 optimum setpoint 10 0 1 2 3 4 [-1 excess air ratio ? Shift of the correbation between CO emissions and excess air ratio due to changing operating conditions. Because the operating conditions permanently change, the new generation of combustion control technique should include information about the amount of unburnt polbutants to guarantee a high efficiency and abow emission level without manual interaction. Information about CO emissions can be used abone. However an increase of CO emissions is easier to interpret, if lambda or the flame temperature is absoknown. An advanced combustion control technique ACCT has been deveboped as an additionab control boop to the existing combinations of bad and combustion control technique [Good and Nussbaumer 1998]. ACCT is based ona CO/Lambda control algorithm. With the use of additional information by measuring Figure 5.1 23 CO emissions, the setpoint of the lambda control loop is permanently optimized. One possibility of setpoint optimization is to reduce the lambda setpoint until an increase of CO emissions is detected. Another is shown in Figure 5.3. Inside a certain range around the actual setpoint lambda control does not change the secondary air. Data of lambda and CO emissions are permanently measured. With exponential forgetting factors, new data are stronger weighted than older data. The shifting of the correlation between CO emissions and excess air ratio due to changing operating conditions can be detected and the setpoint will be adapted. Therefore ACCT maximizes the efficiency with respect to the emissions of unburnt pollutants. increase secondaty air Fuel Input Primary Air Supply pont \ ruvvuv Load Control — PID [ry Control Air Supply no action decrease secondary air / j 3 [mg/m lflflO Furnace T .— Co — —. / / 1‘ co 4 0 1 $2 setpoInt 34 [-15 excess alr ratio Figure 5.2 CO/Lambda control with setpoint opti mization [Good & Nussbaumer 1998]. - Figure 5.3 Principles of the controllers action. ACCT was applied to a 1 MW understoker furnace equipped with bad control and flame temperature control (Figure 5.4). Measurements of emissions and efficiency were done during a whole heating period. CO/Lambda control and the setpoint optimization were first performed by reference measurements of 02 and CO emissions with paramagnetic and infrared analyzers. In a second step ACCT waspertormed by the use of 10w cost, in-situ sensors detecting CO emissions and excess air ra tio. The gas sensor detecting CO emissions is a solid-state, semi-conductor sensor mainly composed )which detects gases through an increase in electrical conductivity when 2 of sintered tin dioxide (SnO reducing gases areabsorbed on the sensors surface, heated at 400 °C The lambda sensor is based on zirconium dioxide (ZrO ). At temperatures above 500 °C the zirconium dioxide as a solid-state 2 electrolyte becomes aconductor of 02 ions. . Figure 5.4 Schematic of a 1 MW understoker furace equipped with ACCT [Good and Nussbaumer 1998] (TIBA-MUELLER AG). 24 Measurements on the 1 MW understoker furnace equipped with ACCT during a whole heating period showed that the efficiency was above 90 % tor the whoe range ot the heat output. Especially at part bad Operation the efficiency was improved by up to 5% compared to flame temperature control. CO emissions averaged over one heating period were below 50 mg/Nm 3 which represents a reduction by a factor of 5 compared to flame temperature control shows, that the selftuning setpoint optimization leads to lower excess air ratios, thus resulting in higher efficiency and lower CO emissions.It has been seen that there is no need tor accurate measurement of CO emissions and lambda. ACCT can there tore be realized by application of 10w cost, in-situ sensors. They can be used tor control and monitoring purposes over long-term periods without calibration and maintenance. Signal drifting of the sensors has no negative etfect on the setpoint optimization algorithm. For typical fuel costs and an expected etticiency improvement over the whole year of 2 to 4 %‚ the investments tor ACCT are estimated to be repaid in 2 to 5 years. For biofuels with bw ash melting points such as grass, miscanthus or urban waste wood, ACCT can be extended in order to avoid an exceeding ot the ash melting temperature. 100 1- uJ ._ :fftLEEf60 ‘“ E o ‘ t a —— Ten,p-Controt with COlLsnibda-Control • Ten,p.-Control a 2-step bad controt, 1988 ZLE 0 0 1 flflfl - A Temp-Control with CO/Larnbda-Control Temp.-Controb !i 2-step bad controb, 1988 - 50___,______,____ 40 30 50 60 70 80 100 90 30 Heat Output [%j Figure 5.5 ‚ Figure 5.6 ------— -— A Temp.-Control with CO/Lambda-Control Temp.-Control • 2-step bad control, 1988 -J 9 :-_J - 11 30 40 50 60 70 80 Heat Figure 5.7 90 50 60 70 80 90 100 Heat Output [%] Etticiency versus heat output, averaged over one heating period. E 40 100 Output [%] Excess air ratio Lambda versus heat output, averaged over one heating period. 25 CO emissions versus heat output, averaged over one heating period. 6 Emissions and Depositions Emissions are dependent on the fue, the design of the furnace, the contro of the furnace and on the cleaning measures applied to the flue gas. A few emissions and possibilities tor their reductions are presented. 6.1 Nitric oxide emissions Nitric oxides from combustion processes are formed in three different reactions: Thermal NO is formed at high temperature from the molecular nitrogen in the air, prompt NO can be formed during the combustion of hydrocarbons and fuel NO,, are formed from the nitrogen caontained in the fuel. NO emissions from biomass combustion originate mainly from fuel nitrogen, since combustion temperature are usually below 1300 °C and thermal NO,, is therefore of minor importance (see Figure 6.1). Typical Biomass Corrdx,stion Thermal NO and Prompt-NO 800 700 I 600 500 400 300 200 H.,b.c.oLi. ‘!f&.ao 100 0 T Fuel NO,,, thermal NO,, and prompt NO,, versus combustion temperature [Nussbaumer 1996]. Figure 6.1 To minimize NO by primary measures, the fuel nitrogen is reduced to molecular nitrogen in zones with an excess air ratio of smaller than 1. The most promising primary measures for the reduction of NO emissions are air staging, fuel staging and flue gas recirculation. NO reductions of 40% 50% for bw and upto 75% tor high nitrogen content can be reached by air staging with a reduction chamber tor the following conditions: primary excess aur ratio = 0.7 0.8, temperature 1,1000 1‘200°C, residence time 0.3 0.5 s. For air staging, flue gas recirculation is proposed to control the temperature and advanced combustion control technmologies are used to ensure an Operation at optimum primary excess air. However, air staging is not suited tor biofuels with bw ash melting point since the high temperature can lead to siagging. Fuel staging shows a similar potential of NO,, reduction and it is mainly feasable for barger plants [Nussbaumer 1996]. Possible secondary measures tor the reduction of NO emissions are the selective catalytic and non catalytic reduction (SCR, SNCR) by injection of ammonia or urea. 60% 80% NO,, reduction can be reached with SNCR. The NO,, reduction is Iimited by the ammonia slippage and an accurate process - — — — - 26 control is necessary to ensure the temperature windiw of 840°C 920°C. Up to 95% NO reduction can be ach ieved with SCR. For large plants, combinations of 10w NO and denox-techniques are considered. Furthermore, biofuels can be used as effective reburn fuels for the NO reduction in coa fired power stations. The potential of different primary and secondary measures at different fuel nitrogen content is shown in Figure 6.2. - 2 NOx asNO 1000i 1 NO 3 [mg/Nm 2 atll%0 - . - 1 Conventional ibustion LOWNO with Air Staging and Reductlon Chamber V/SCR 10 0.01 Grass Straw Urban Waste Wood Miscanthus 4 UFChipBOardS NativeWood 0.1 1 [wt.-%] 10 FueI-N Figure 6.2 6.2 Comparison of NO emissions versus fuel nitrogen tor different measures. Particle emissions As the efficiency of particle separators and filters is dependent on the size of the particies, it is important to know the particle size distribution of fly ash. The particle size distribution of fly ash was determined with an Andersen cascade impactor for various fuels in different furnaces and under different operating conditions in [Hasler and Nussbaumer 1997 & 1998]. Particle diameters are calculated as aerodynamic diameters (unit particle density of p = 1.0 kg/dm ). For 3 native wood, chipboard fuel, urban waste wood and hay, un[modal particle size distributions with a mean diameter of less than 0.25 jm were found. More than 80% of the particle mass was found to be aerosols with a diameter of smaller than 1im (see Figure 6.3). Bark is the only fuel found so far which exhibits a bimodal particle size distribution. Flue gas recirculation Ieads to lower amounts of aerosol particies in under stoker furnaces. Fly ash from herbage-grass and wheat straw has been analysed closer with regard to composition and shape and is tound to consist mainly of potassium chloride (KCI). The shape of the fly ash consists of crystalline particies having the typical cubic shape of the main compound, KCI. This is in clear Opposition to fly ash from wood, which appears in amorphous shape (see Figure 6.4). 27 Native wood Irnbd 2.72 TotI 4451 0ontnt 75 = — Native wood / bark mixture 78 rng/Nr<3 (11% 02) = 1.81 To511 d<st 005tent 75 = 72 rng/Nnt3 (11% 02) 5° 50 z E 25 25 c 0 0 1.) (3 0 <0.22 0.22 0.35 0.61 1.28 2.03 3.01 4.48 «0.21 7.22 8) = °Q 0.21 150 Urban waste wood ntbds 328 Totsl dont sontont 0.34 0.60 1.27 2.02 2.99 4.46 7.19 Aerodyn. particle diameter [sm1 Aerodyn. particle diameter [)Jm] = — Hay pellets O 206 rng/Nm3 )l 1% 02) 6mbd=a5 lolol dost oontont 1 125 100 z 300 = 250 200 150 50 100 25 <0.22 0.22 0.35 0.61 1.28 2.04 3.03 4.50 7.26 <0.26 0.26 Aerodyn. particle diameter [pmj Figure 6.3 — 0 519 tng/Nnt3 111% 02) 0.41 0.71 1.48 2.35 3.47 5.16 8.30 1 Aerodyn. particle diameter [)im] Particle size distribution during the combustion of native wood, a mixture of native wood and bark, urban waste wood and hay peflets in a 450 kW moving grate furnace at full bad [Hasler and Nussbaumer 1998]. (a) (b) Figure 6.4 Fly ash particies from herbage-grass (a), wheat straw (b) and wood (c) collected on polycarbonate filters [Kaufmann and Nussbaumer 1998]. (c) 28 6.3 Particle separation in a rotating particle separator The Rotating Partiole Separator RPS [Brouwers 1995 & 1997] is a new design of a particle separator which has been investigated for the use in biomass furnaces [Hasler et al. 1997 and 1998]. T T Top view ot the RPS RPS with cyclone and rotating cylinder Rotating cylinder with axial capillaries Figure 6.5: Diagram of the RPS (tangential version) [Brouwers 1995] The particle collection efficiency has been experimentally verified as a function of the dimensionsless partiole diameter. The effective d 0 max was found to be higher by a factor of approximately 1.5 than the calculated value d 1 The RPS will also separate smaller particles than the it is designed tor, but with a lower efficiency. In oase of the so-called tangential design appropriate tor flue gas filtering the separation efficiency tor particles with d = 0.5 is approx. 70%, tor d = 0.25 the efliciency is approx. 50%. Cleaning of the particle baden cylinder channels is done by injecting compressed air from the top ot the rotating filter element through a nozzle. Dedustirig can be made during filter Operation. The nominal operating conditions for the RPS tested are as follows: • • • Filter element rotating speed 360 rad/s Gas temperature 200°C Flow rate 1800 Am /h 3 The calculated value tor d 0 max is 1.8 jim. 29 In a 450 kW moving grate furnace, the particle collection efficiencies have been determined during the combustion of saw dust (Figure 6.6). The RPS was operated at 350 radls (3300 rpm) and the flow rate /h. 3 was 900 Am 100 A 0 >‘ 0 80 *0 * Measurement na. 0 cl) c 60 c) 40 0 0 . oMeasurement no. 4J-_-_-______ 0 0 0 0) () 20 ccl 0 0.00 2.00 4.00 6.00 8.00 [-1 Figure 6.6: RPS particle collection efficiencies from test runs during saw dust combustion A series of particle mass measurements has been made in the clean gas of the RPS with variing angular velocitites of the filter element. Native wood chips were used as a fuel. The liow rate entering the RPS /h. Raw gas particle concentrations were observed from 50 to 120 mg/Nm 3 was 900 Am 3 in previous tests. Although the residual particle emissions exhibit some variations, there is a tendency of lower emissions with increasing angular velocity. In total 11 measurements were made and two values exceeded the target dust concentration of 50 mg/Nm 3 (at 11% 02). 70 E target value 0 z E 0 60 50 0 40 00 0 0) 0 0 cl) (.) (cl 0 0 30 0 20 0 10 0 200 250 300 350 400 450 Angular velocity [rad/s] Figure 6.7: Residual particle emissions after RPS during the combustion of native wood chips in a 450 kW moving grate furnace 30 6.4 Chlorine emissions As the combustion of herbage-grass, miscanthus, hay and straw causes higher emissions of particies, more deposition is encountered in the boiler and in the heat exchanger. The high particie emissions mailny resuit from the volatile minerals contained in grass and straw. Suifur is emitted as a salt 4 S0 or 2 (K ) as SO 2 and SO . if the combustion is incompiete sulfur is also emitted as H 3 S. Chiorine can occur in the 2 fiue gas in the form of sait (KC1, NaC1) or as HC1 as weil as in dioxines and organic chiorine compouds. Own measurements and data from literature show that most of the chiorine is emitted as salt. The concentration of HCI is usuaiiy between 20 and 120 mg/Nm 3 (see Figure 6.8). lt is assumed, that the 10w HCI concentrations result from the high concentrations of K and Na, that react with the chiorine. 120 1 100 (1) • Herbage-gr. Timo1he Feedgr. mix • W. straw > Hemp OMisc. Sedge 80 ci, E z 60 0 0 0.1 v ci, 40 0 0 20 0 - z 0 0.01 0 o 0.005 0.01 0.015 Fuel chiorine content [kg/kg DS] Figure 6.8 0.0025 0.005 0.0075 0.01 Fuel chiorine content [kg/kg DS] HCI emissions as a function of the chiorine content in the fuel (left hand side) and the transfer rate of fuel chiorine to HCI (right hand side) [Kaufmann 1997] 31 calculated tor 11 vol% 02 5000 Dust [mg/Nm ] 3 Area sum of contents 4000 3000 Grass Straw Miscanthus Wood 2000 Measured dust concentrations in raw gas Grass 1000 Slraw 111111111 0 Sum of K, Cl, S content in fuel [weight-%] Figure 6.9 Dust content in the raw gas (flue gas after the cycione) tor combustion of grass, straw and miscanthus. The maximum concentration of salts for the complete emission of potassium, chiorine and sulfur in the tlue gas is given tor comparison. * Deposition, condensation, crystallization Figure 6.10 Path of potassium, chlorine and sulfur ot the fuel in the furnace. 6.5 Deposit formation During the combustion of herbage-grass (hay), miscanthus and straw in a grate furnace, intensive deposit formation was observed on the combustion chamber walls (brick) and on the boiler walls (steel). Although it is obvious, that the deposits are caused by the fly ash, the formation mechanisms of de positions are not yet known in detail. The aim of the present investigation was to analyze the chemical and morphological properties, to identifiy the mechanisms of deposition formation, and to propose measures for deposition reduction. Depositions from bioniass are accumulations of fine particles in the 32 nanometer range, whose chemism is dominated by the properties of potassium chiorine, the major compound found in the deposition. Among the known formation mechanisms, thermophoresis revealed to be the crucial process for depositions from biomass combustion. The resuits of the investigation are presented in [Kaufmann et al. 1998]. Table 6.1 gives an overview of the composition of the different depositions found in the Multif Fuel Combustor at Sandia and in a grate furnace operated in Switzerland. Table 6.1 Composition of the sticky deposition on a single cylinder in the plug flow reactor compared to the composition of deposits in the bauer of a 450 kWth grate furnace in [wt.-%] MFC MFC Grate furnace Fieldgrass Miscanthus Fieldgrass Sticky deposit Sticky deposit Fuel Deposition End of pipe Beginn of pipe ER 12—1.5 2—2.3 12—1.5 2—2.3 2—2.3 2—2.3 Dim. [wt.-%] [wt.-%] [wt.-%] [wt.-%] [wt.-%] [wt.-%] 53.9 K 27.72 30.1 10.3 iZi 46.8 S 6.76 1.94 11.5 1.45 12.32 2.7 CI 12.4 13 2 8.37 24.7 33.4 Si 18.25 10.0 21.7 20.5 1.09 0.14 Ca 9.58 7.51 4.57 5 1.48 0.16 Na 0.82 1.16 11.5 1.13 0.660 0.71 P 4.62 2.59 1.39 1.49 1.05 0.07 Mg 2.82 2.15 1.13 1.16 0.316 0.02 Ti 0.086 0.07 0.04 0.04 0.069 <0.01 Fe 123 0.7 1.12 126 1.29 <0.01 Al 0.84 1.32 0.8 0.79 0.40 0.16 C 0.13 0.4 0.48 0.75 0.066 0.016 Sum: 85.6 71.7 67.7 55.6 90.4 91.4 Figure 6.11 FIy ash deposition on bauer surfaces of the grate furnace [Kaufmann and Nussbaumer 1998]. 33 6.6 Dioxins and furans Polychlorinated dioxins and furans (PCDD and PCDF) have been determined during the combustion of wood and herbaceous biofuels in different furnaces (Nussbaumer and Hasler 1996]. PCDD/F are found to be a consequence of the de novo synthesis in the temperature window between 180°C and 500°C. Carbon, chiorine, cataiysts (copper) and oxygen are necessary for the formation of PCDD/F. Emissions from non contaminated wooci were usually below 0.1 ng TE/Nm 3 at 11 vol.-% 02, while from 3 were found, ranging from 0.03 the combustion of urban waste wood emissions of app. 2 ng TEINm . The combustion of charcoal in a wood stove resulted in the very bw PCDD/F emissions 3 18 ng TE/Nm , while combustibbe household waste Iead to extremely high emissions. Although 3 of 0.028 ng TE/Nm . This is 3 herbaceous biofuels have high chiorine contents, PCDD/F are usualiy below 0.1 ng TEINm explained by the high alkali content, which Ieads to the formation of saits (KCI, NaCI) and to a lower level of gaseous chiorine for the de novo synthesis. Primary measures to avoid dioxin emissions are a complete burn out of the fly ash and an Operation of the combustion at 10w air excess (02 < 11 vol.-%, prefereably <6%) and under stable conditions. For automatic wood furnaces an efficient particle Separation iS needed and the filter must be operated weil below the temperature of the de novo synthesis. Furthermore adsorptives such as activated lignite can 2 and PCDD/F in filters. However illegal incineration of be used for a combined extraction of HCI, SO wastes in wood furnaces must be strictly avoided. — dust burner moving grate understoker preoven log wood boiler ooen chimney wood stove —I — 0.00 0.20 0.10 0.40 0.60 0.80 PCDD/F emission [ng TEINm ] 3 1.00 Figure 6.12 PCDD/F emissions in the clean gas from the combustion of uncontaminated wood at 11 vol.-% 02, 1-TEF acc. to NATO-CCMS [Nussbaumer and Hasler 1996]. 34 7 References Baxter, L.; Miles, Th. ; Miles, Th. (Jr.); Jenkins, B.; Dayton, D.; Milne, Th.; Bryers, R.; Oden, L.: Alkali Deposits found in Biomass Bollers, Sandia National Laboratory, Livermore (CA, USA) 1996 Baxter, L.L., Jenkins, B.M., Miles, T.R. e.a. (1994). Alkalis in alternative biofuels. 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