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ScienceDirect

Available online at www.sciencedirect.comAvailable online at www.sciencedirect.com

ScienceDirect

Energy Procedia 00 (2017) 000–000

www.elsevier.com/locate/procedia

1876-6102 © 2017 The Authors. Published by Elsevier Ltd.

Peer-review under responsibility of the Scientific Committee of The 15th International Symposium on District Heating and Cooling.

The 15th International Symposium on District Heating and Cooling

Assessing the feasibility of using the heat demand-outdoor temperature function for a long-term district heat demand forecast

I. Andrić

a,b,c

*, A. Pina

a

, P. Ferrão

a

, J. Fournier

b

., B. Lacarrière

c

, O. Le Corre

c

aIN+ Center for Innovation, Technology and Policy Research - Instituto Superior Técnico, Av. Rovisco Pais 1, 1049-001 Lisbon, Portugal

bVeolia Recherche & Innovation, 291 Avenue Dreyfous Daniel, 78520 Limay, France

cDépartement Systèmes Énergétiques et Environnement - IMT Atlantique, 4 rue Alfred Kastler, 44300 Nantes, France

Abstract

District heating networks are commonly addressed in the literature as one of the most effective solutions for decreasing the greenhouse gas emissions from the building sector. These systems require high investments which are returned through the heat sales. Due to the changed climate conditions and building renovation policies, heat demand in the future could decrease, prolonging the investment return period.

The main scope of this paper is to assess the feasibility of using the heat demand – outdoor temperature function for heat demand forecast. The district of Alvalade, located in Lisbon (Portugal), was used as a case study. The district is consisted of 665 buildings that vary in both construction period and typology. Three weather scenarios (low, medium, high) and three district renovation scenarios were developed (shallow, intermediate, deep). To estimate the error, obtained heat demand values were compared with results from a dynamic heat demand model, previously developed and validated by the authors.

The results showed that when only weather change is considered, the margin of error could be acceptable for some applications (the error in annual demand was lower than 20% for all weather scenarios considered). However, after introducing renovation scenarios, the error value increased up to 59.5% (depending on the weather and renovation scenarios combination considered).

The value of slope coefficient increased on average within the range of 3.8% up to 8% per decade, that corresponds to the decrease in the number of heating hours of 22-139h during the heating season (depending on the combination of weather and renovation scenarios considered). On the other hand, function intercept increased for 7.8-12.7% per decade (depending on the coupled scenarios). The values suggested could be used to modify the function parameters for the scenarios considered, and improve the accuracy of heat demand estimations.

© 2017 The Authors. Published by Elsevier Ltd.

Peer-review under responsibility of the Scientific Committee of The 15th International Symposium on District Heating and Cooling.

Keywords:Heat demand; Forecast; Climate change

Energy Procedia 142 (2017) 395–400

1876-6102 © 2017 The Authors. Published by Elsevier Ltd.

Peer-review under responsibility of the scientific committee of the 9th International Conference on Applied Energy.

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gasification and combustion. Besides the main solid product, a number of by-products including water, carbon dioxide (CO2), carbon monoxide (CO), and various organic compounds can be obtained after torrefaction. They can be classified into two groups: non-condensable and condensable volatiles, although they are all volatiles when formed at the torrefaction temperature. The former are permanent gases, while the latter becomes liquid after cooled to room temperature.

Recently, research and development activities on biomass torrefaction have been very active to look at the torrefaction characteristic of a wide range of biomass species and to investigate the effects of torrefaction parameters (e.g., temperature and residence time) on the fuel properties of the torrefied products [5-10]. However, most of them are experimental studies, from which information for up-scaling the process is limited. In order to fulfill the research gap between academia and industry, process modeling studies are required.

This work aims to build a complete torrefaction model for Norwegian birch branches using a commercial simulator. The model can provide a detailed distribution of main torrefied products and by-products at various torrefaction conditions. The heating value of the main solid product after torrefaction can be predicted and are compared with available experimental data. More importantly, the overall energy consumption and the process energy efficiency are estimated and presented.

Table 1. Description of all units and streams in the torrefaction model.

Unit or stream Classification Description Operating temperature (°C)

DRY-AIR Cold stream Air at ambient temperature 25

HX-AIRDR Heater Drying air heater

HOT-AIR Hot stream Hot inlet drying air 180

DRIER Block Drying unit

EXHAUST Hot stream Hot outlet drying air 110

HX-EXH Cooler Outlet drying air cooler

COLD-AIR Cold stream Cooled drying air 50

DRY-BIOM Hot stream Hot dried biomass 110

N2-COLD Cold stream Nitrogen at ambient temperature 25

TOREFIER Block Torrefaction unit 240–300

TOR-BIOM Hot stream Torrefied biomass stream 240–300

BYPROD Hot stream By-products stream 240–300

HX-COOL Cooler Product cooler

PROD Cold stream Final torrefied biomass product 50

COMB-AIR Cold stream Air fed to combustor 25

COMBSTOR Block Combustion unit

HOT-FG Hot stream Hot flue gas

HX-FG Cooler Flue gas cooler

COLD-FG Cold stream Cold flue gas 50

2. Methodology

2.1. Torrefaction process flow diagram

The flow diagram of the torrefaction model in Aspen Plus v8.8 is illustrated in Figure 1. Description of all units and streams are presented in Table 1.

Fig. 1. Flow diagram of the torrefaction model.

2.2. Feedstock and torrefaction reactions

Norway birch branches, i.e. a forest residue, were chosen as the feedstock in this study. Available data for the fuel properties of the feedstock are adopted from another work [11] and presented in Table 2. The initial feedstock was assumed to have a moisture content of 50%, which is close to its measured value (56.31 ± 1.93 wt%) directly after harvesting, and the moisture content has been set to reduce to 10% prior to entering the torrefaction reactor.

Table 2. Fuel properties of feedstock.

Moisture contenta Proximate analysisb Ultimate analysisb

Ash VM FC C H N O

Norway birch branches 50 0.64 89.73 9.63 48.24 6.15 0.16 44.81

awt%, wet basis; bwt%, dry basis

If it is assumed that biomass contains only carbon, hydrogen, oxygen, nitrogen, sulfur and ash, a general chemical formula for biomass is �, where �,�,�,�, and � represent the elements and � represents ash in biomass, and subscript letters are calculated from the ultimate analysis of the fuel. A torrefaction reaction, based on a previous study by Bates and Ghoniem [12], can be given as in Eq. (1):

������������ ����

������������������ �����

��

��

��

������ �

���� ��

���� ��

���� ��

���� ��

���� �

���� �

���� �

���� �

(1)

where � and � represent the raw and torrefied biomass; � is the mass yield of the torrefied biomass; the Greek characters denote the mass yields of the corresponding by-products.

2.3. Assumptions

Some assumptions are made for the process simulations:

• The stream class used in the model is MIXCISLD, in which raw and torrefied biomass are considered as non-conventional solids.

• The properties method is Redlich-Kwong-Soave (RKS).

• All calculations are in steady-state.

DRIER

COMBSTOR

HX-COOL HX-AIRDR

HX-FG HX-EXH

H TOREFIER

TOR-BIOM TOR-GAS FEED

EXHAUST

HOT-AIR

HOT-FG COMB-AIR

DRY-AIR PROD

DRY-BIOM

N2-COLD

COLD-FG COLD-AIR

(3)

gasification and combustion. Besides the main solid product, a number of by-products including water, carbon dioxide (CO2), carbon monoxide (CO), and various organic compounds can be obtained after torrefaction. They can be classified into two groups: non-condensable and condensable volatiles, although they are all volatiles when formed at the torrefaction temperature. The former are permanent gases, while the latter becomes liquid after cooled to room temperature.

Recently, research and development activities on biomass torrefaction have been very active to look at the torrefaction characteristic of a wide range of biomass species and to investigate the effects of torrefaction parameters (e.g., temperature and residence time) on the fuel properties of the torrefied products [5-10]. However, most of them are experimental studies, from which information for up-scaling the process is limited. In order to fulfill the research gap between academia and industry, process modeling studies are required.

This work aims to build a complete torrefaction model for Norwegian birch branches using a commercial simulator. The model can provide a detailed distribution of main torrefied products and by-products at various torrefaction conditions. The heating value of the main solid product after torrefaction can be predicted and are compared with available experimental data. More importantly, the overall energy consumption and the process energy efficiency are estimated and presented.

Table 1. Description of all units and streams in the torrefaction model.

Unit or stream Classification Description Operating temperature (°C)

DRY-AIR Cold stream Air at ambient temperature 25

HX-AIRDR Heater Drying air heater

HOT-AIR Hot stream Hot inlet drying air 180

DRIER Block Drying unit

EXHAUST Hot stream Hot outlet drying air 110

HX-EXH Cooler Outlet drying air cooler

COLD-AIR Cold stream Cooled drying air 50

DRY-BIOM Hot stream Hot dried biomass 110

N2-COLD Cold stream Nitrogen at ambient temperature 25

TOREFIER Block Torrefaction unit 240–300

TOR-BIOM Hot stream Torrefied biomass stream 240–300

BYPROD Hot stream By-products stream 240–300

HX-COOL Cooler Product cooler

PROD Cold stream Final torrefied biomass product 50

COMB-AIR Cold stream Air fed to combustor 25

COMBSTOR Block Combustion unit

HOT-FG Hot stream Hot flue gas

HX-FG Cooler Flue gas cooler

COLD-FG Cold stream Cold flue gas 50

2. Methodology

2.1. Torrefaction process flow diagram

The flow diagram of the torrefaction model in Aspen Plus v8.8 is illustrated in Figure 1. Description of all units and streams are presented in Table 1.

Fig. 1. Flow diagram of the torrefaction model.

2.2. Feedstock and torrefaction reactions

Norway birch branches, i.e. a forest residue, were chosen as the feedstock in this study. Available data for the fuel properties of the feedstock are adopted from another work [11] and presented in Table 2. The initial feedstock was assumed to have a moisture content of 50%, which is close to its measured value (56.31 ± 1.93 wt%) directly after harvesting, and the moisture content has been set to reduce to 10% prior to entering the torrefaction reactor.

Table 2. Fuel properties of feedstock.

Moisture contenta Proximate analysisb Ultimate analysisb

Ash VM FC C H N O

Norway birch branches 50 0.64 89.73 9.63 48.24 6.15 0.16 44.81

awt%, wet basis; bwt%, dry basis

If it is assumed that biomass contains only carbon, hydrogen, oxygen, nitrogen, sulfur and ash, a general chemical formula for biomass is �, where �,�,�,�, and � represent the elements and � represents ash in biomass, and subscript letters are calculated from the ultimate analysis of the fuel. A torrefaction reaction, based on a previous study by Bates and Ghoniem [12], can be given as in Eq. (1):

������������ ����

������������������ �����

��

��

��

������ �

���� ��

���� ��

���� ��

���� ��

���� �

���� �

���� �

���� �

(1)

where � and � represent the raw and torrefied biomass; � is the mass yield of the torrefied biomass; the Greek characters denote the mass yields of the corresponding by-products.

2.3. Assumptions

Some assumptions are made for the process simulations:

• The stream class used in the model is MIXCISLD, in which raw and torrefied biomass are considered as non-conventional solids.

• The properties method is Redlich-Kwong-Soave (RKS).

• All calculations are in steady-state.

DRIER

COMBSTOR

HX-COOL HX-AIRDR

HX-FG HX-EXH

H TOREFIER

TOR-BIOM TOR-GAS FEED

EXHAUST

HOT-AIR

HOT-FG COMB-AIR

DRY-AIR PROD

DRY-BIOM

N2-COLD

COLD-FG COLD-AIR

(4)

• The system operates at atmospheric pressure and all pressure drops are neglected.

• Air consists of 79% nitrogen and 21% oxygen on molar basis.

• The ambient temperature is 25 °C, i.e. supplied air and nitrogen enter corresponding blocks at 25 °C.

• The hot streams (EXHAUST, HOT-FG, and TOR-BIOM) are cooled to 50 °C.

• Heat losses are assumed to be 10% of the heat produced from or supplied to blocks.

3. Preliminary results and discussion

3.1. Products distribution and characterizations

The simulation was carried out at different torrefaction temperatures, from 240 to 300 °C. A torrefaction time of 30 min was selected and kept constant because the effect of time is less pronounced than that of temperature. In addition, a flow rate of 200 kg wet feedstock per hour was chosen for this simulation.

Fig. 2. Plots of mass yield, energy yield and heating values of torrefied biomass at different temperatures.

Simulation results for the mass and energy yields as well as the heating values of the torrefied biomass at different temperatures are presented in Fig. 2. It can be seen from the figure that both the mass and energy yields of the torrefied biomass decrease while its heating value increases with increasing torrefaction temperature. When the temperature increases from 240 to 300 °C, the mass and energy yields reduce respectively from 92.2 to 63.2% and from 98.7 to 80.6%; on the other hand, the heating value is raised from 20.6 to 24.8 MJ/kg. Increased heating value of torrefied biomass is attributed to changes in their elemental composition.

Fig. 3 presents the mass yield distribution of the by-products after torrefaction at different temperatures. It can be seen from the figure that more by-products are produced when increasing the torrefaction temperature, which is consistent with the decreasing mass yield trend of the torrefied biomass. Among the by-products, water is the most dominant (4.1-13.2%), followed by carbon dioxide (2.4-4.8%). Methanol is a minor component at low temperatures but its contribution increases greatly and is even higher than carbon dioxide at high temperatures. Other by-products play minor parts because most of them account for less than 4.4% at the highest temperature (i.e., 300 °C).

20 21 21 22 22 23 23 24 24 25 25

50 55 60 65 70 75 80 85 90 95 100

230 240 250 260 270 280 290 300 310

HHV (MJ/kg)

Yield (%)

Temperature (°C) Mass yield Energy yield Heating value

Fig. 3. Distribution of torrefaction by-products at different temperatures.

3.2. Heat required/produced and thermal energy efficiency

The heat required and produced as well as thermal energy efficiency of the torrefaction process at different temperatures are extracted from the simulations and presented in Table 3.

Table 3. Heat required/produced and thermal energy efficiency of torrefaction process.

Torrefaction temperature (°C)

Heat required/produced (kW) Energy efficiency Drying Torrefaction Utilities (%)

240 -100.9 -23.1 32.4 92.9

245 -100.9 -23.6 35.2 92.7

250 -100.9 -24.1 38.6 92.5

255 -100.9 -24.7 42.5 92.2

260 -100.9 -25.3 47.0 91.9

265 -100.9 -25.9 52.1 91.6

270 -100.9 -26.6 57.7 91.3

275 -100.9 -27.3 63.9 90.9

280 -100.9 -28.0 70.6 90.5

285 -100.9 -28.8 77.9 90.1

290 -100.9 -29.6 85.7 89.6

295 -100.9 -30.5 94.1 89.1

300 -100.9 -31.3 103.0 88.5

It can be seen from the table that it requires about 100.9 kW to dry 200 kg feedstock per hour from 50% to 10%

moisture. In other words, drying accounts for 76-81% of the total heat required for the whole process. This observation is in good agreement with other literature showing that drying is an energy intensive step [13-15].

Because the feedstock flow rate is kept constant, the drying energy is thus unchanged with the torrefaction temperature. The table also reveals that sustaining the torrefaction process needs only 19-24% of the total heat required for the whole process, i.e., 23.1-31.3 kW, depending on the torrefaction temperature: the higher the torrefaction temperature is the more energy it requires. Compared to the drying energy, heat demanded for torrefaction is 3.2-4.3 times less. Another important information is the utilized energy, which is from 32.4 kW at a torrefaction temperature of 240 °C to 103.0 kW at a torrefaction temperature of 300 °C. More energy is collected

0 2 4 6 8 10 12 14

230 240 250 260 270 280 290 300 310

Yield (%)

Temperature (°C)

H2O CO2 CO Methanol Formic acid Acetic acid Hydroxyacetone Lactic acid Furfural

(5)

• The system operates at atmospheric pressure and all pressure drops are neglected.

• Air consists of 79% nitrogen and 21% oxygen on molar basis.

• The ambient temperature is 25 °C, i.e. supplied air and nitrogen enter corresponding blocks at 25 °C.

• The hot streams (EXHAUST, HOT-FG, and TOR-BIOM) are cooled to 50 °C.

• Heat losses are assumed to be 10% of the heat produced from or supplied to blocks.

3. Preliminary results and discussion

3.1. Products distribution and characterizations

The simulation was carried out at different torrefaction temperatures, from 240 to 300 °C. A torrefaction time of 30 min was selected and kept constant because the effect of time is less pronounced than that of temperature. In addition, a flow rate of 200 kg wet feedstock per hour was chosen for this simulation.

Fig. 2. Plots of mass yield, energy yield and heating values of torrefied biomass at different temperatures.

Simulation results for the mass and energy yields as well as the heating values of the torrefied biomass at different temperatures are presented in Fig. 2. It can be seen from the figure that both the mass and energy yields of the torrefied biomass decrease while its heating value increases with increasing torrefaction temperature. When the temperature increases from 240 to 300 °C, the mass and energy yields reduce respectively from 92.2 to 63.2% and from 98.7 to 80.6%; on the other hand, the heating value is raised from 20.6 to 24.8 MJ/kg. Increased heating value of torrefied biomass is attributed to changes in their elemental composition.

Fig. 3 presents the mass yield distribution of the by-products after torrefaction at different temperatures. It can be seen from the figure that more by-products are produced when increasing the torrefaction temperature, which is consistent with the decreasing mass yield trend of the torrefied biomass. Among the by-products, water is the most dominant (4.1-13.2%), followed by carbon dioxide (2.4-4.8%). Methanol is a minor component at low temperatures but its contribution increases greatly and is even higher than carbon dioxide at high temperatures. Other by-products play minor parts because most of them account for less than 4.4% at the highest temperature (i.e., 300 °C).

20 21 21 22 22 23 23 24 24 25 25

50 55 60 65 70 75 80 85 90 95 100

230 240 250 260 270 280 290 300 310

HHV (MJ/kg)

Yield (%)

Temperature (°C) Mass yield Energy yield Heating value

Fig. 3. Distribution of torrefaction by-products at different temperatures.

3.2. Heat required/produced and thermal energy efficiency

The heat required and produced as well as thermal energy efficiency of the torrefaction process at different temperatures are extracted from the simulations and presented in Table 3.

Table 3. Heat required/produced and thermal energy efficiency of torrefaction process.

Torrefaction temperature (°C)

Heat required/produced (kW) Energy efficiency Drying Torrefaction Utilities (%)

240 -100.9 -23.1 32.4 92.9

245 -100.9 -23.6 35.2 92.7

250 -100.9 -24.1 38.6 92.5

255 -100.9 -24.7 42.5 92.2

260 -100.9 -25.3 47.0 91.9

265 -100.9 -25.9 52.1 91.6

270 -100.9 -26.6 57.7 91.3

275 -100.9 -27.3 63.9 90.9

280 -100.9 -28.0 70.6 90.5

285 -100.9 -28.8 77.9 90.1

290 -100.9 -29.6 85.7 89.6

295 -100.9 -30.5 94.1 89.1

300 -100.9 -31.3 103.0 88.5

It can be seen from the table that it requires about 100.9 kW to dry 200 kg feedstock per hour from 50% to 10%

moisture. In other words, drying accounts for 76-81% of the total heat required for the whole process. This observation is in good agreement with other literature showing that drying is an energy intensive step [13-15].

Because the feedstock flow rate is kept constant, the drying energy is thus unchanged with the torrefaction temperature. The table also reveals that sustaining the torrefaction process needs only 19-24% of the total heat required for the whole process, i.e., 23.1-31.3 kW, depending on the torrefaction temperature: the higher the torrefaction temperature is the more energy it requires. Compared to the drying energy, heat demanded for torrefaction is 3.2-4.3 times less. Another important information is the utilized energy, which is from 32.4 kW at a torrefaction temperature of 240 °C to 103.0 kW at a torrefaction temperature of 300 °C. More energy is collected

0 2 4 6 8 10 12 14

230 240 250 260 270 280 290 300 310

Yield (%)

Temperature (°C)

H2O CO2 CO Methanol Formic acid Acetic acid Hydroxyacetone Lactic acid Furfural

(6)

from the utilities at higher torrefaction temperature because more by-products are produced and thus more heat is extracted at HX-COOL. Furthermore, Table 3 also exposes a decreasing trend in the thermal energy efficiency of the process when increasing the torrefaction temperature, which is due to increased heat loss with increasing torrefaction temperatures.

4. Conclusion

A complete torrefaction model has been built in the Aspen Plus v8.8 software. Norwegian forest residue (birch branches) was chosen as the feedstock. The model is capable to provide the distribution of both the torrefied biomass and by-products.

Simulation results show good agreement with available data in the literature. Increasing the torrefaction temperature leads to reduction in both the mass and energy yields of the torrefied biomass but increase in the heating value. The model also reveals that drying accounts for 76-81% of the total heat demand. More importantly, the process energy efficiency reduces with increasing temperature, thus torrefaction at high temperatures is not recommended. The information obtained from this work would be important for industrialization and commercialization of the torrefaction process.

Acknowledgements

This research was supported by the Chung-Ang University Research Grants.

References

[1] M. J. C. van der Stelt, H. Gerhauser, J. H. A. Kiel, and K. J. Ptasinski, "Biomass upgrading by torrefaction for the production of biofuels: A review," Biomass and Bioenergy, vol. 35, pp. 3748-3762, 2011.

[2] D. Ciolkosz and R. Wallace, "A review of torrefaction for bioenergy feedstock production," Biofuels, Bioproducts and Biorefining, vol. 5, pp. 317-329, 2011.

[3] J. J. Chew and V. Doshi, "Recent advances in biomass pretreatment – Torrefaction fundamentals and technology," Renewable and Sustainable Energy Reviews, vol. 15, pp. 4212-4222, 2011.

[4] W.-H. Chen, J. Peng, and X. T. Bi, "A state-of-the-art review of biomass torrefaction, densification and applications," Renewable and Sustainable Energy Reviews, vol. 44, pp. 847-866, 2015.

[5] W.-H. Chen, H.-C. Hsu, K.-M. Lu, W.-J. Lee, and T.-C. Lin, "Thermal pretreatment of wood (Lauan) block by torrefaction and its influence on the properties of the biomass," Energy, vol. 36, pp. 3012-3021, 2011.

[6] W.-H. Chen, W.-Y. Cheng, K.-M. Lu, and Y.-P. Huang, "An evaluation on improvement of pulverized biomass property for solid fuel through torrefaction," Applied Energy, vol. 88, pp. 3636-3644, 2011.

[7] M. J. Prins, K. J. Ptasinski, and F. J. J. G. Janssen, "Torrefaction of wood: Part 1. Weight loss kinetics," Journal of Analytical and Applied Pyrolysis,vol. 77, pp. 28-34, 2006.

[8] M. J. Prins, K. J. Ptasinski, and F. J. J. G. Janssen, "Torrefaction of wood: Part 2. Analysis of products," Journal of Analytical and Applied Pyrolysis,vol. 77, pp. 35-40, 2006.

[9] D. Medic, M. Darr, A. Shah, B. Potter, and J. Zimmerman, "Effects of torrefaction process parameters on biomass feedstock upgrading,"

Fuel, vol. 91, pp. 147-154, 2012.

[10] B. Arias, C. Pevida, J. Fermoso, M. G. Plaza, F. Rubiera, and J. J. Pis, "Influence of torrefaction on the grindability and reactivity of woody biomass," Fuel Processing Technology, vol. 89, pp. 169-175, 2008.

[11] Q.-V. Bach, K.-Q. Tran, and Ø. Skreiberg, "Hydrothermal pretreatment of fresh forest residues: Effects of feedstock pre-drying," Biomass and Bioenergy, vol. 85, pp. 76-83, 2016.

[12] R. B. Bates and A. F. Ghoniem, "Biomass torrefaction: Modeling of volatile and solid product evolution kinetics," Bioresource Technology, vol. 124, pp. 460-469, 2012.

[13] H. Li, Q. Chen, X. Zhang, K. N. Finney, V. N. Sharifi, and J. Swithenbank, "Evaluation of a biomass drying process using waste heat from process industries: A case study," Applied Thermal Engineering, vol. 35, pp. 71-80, 2012.

[14] L. Fagernäs, J. Brammer, C. Wilén, M. Lauer, and F. Verhoeff, "Drying of biomass for second generation synfuel production,"Biomass and Bioenergy, vol. 34, pp. 1267-1277, 2010.

[15] H. Holmberg and P. Ahtila, "Comparison of drying costs in biofuel drying between multi- stage and single-stage drying," Biomass and Bioenergy, vol. 26, pp. 515-530, 2004.

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Comparing the particle size distribution of the ground raw and torrefied samples we can conclude, that by applying more severe torrefaction before the grinding, the

Upon torrefaction treatment, the durability and strength of the studied wood, bark, and forest residue pellets were decreased, which correlated well with the improvement of

[32] T. Hupa, "Ash- Forming Matter in Torrefied Birch Wood: Changes in Chemical Association," Energy & Fuels, vol. Williams, "Physicochemical characterisation of

Related research recommends a user-centered design process, the involvement of individuals with a wide range of abilities and disabilities, and to have user participation in

I grew interested in trying to understand the American approach and the reasons behind the current American influence in medicine, and left The Norwegian University of Science

partially stirred stochastic reactor allows detailed modeling of the multi-phase nature of biomass conversion.. State

2 shows, the residence time had no significant effect on the composition of the torrefied samples up to 275°C, while at 300 °C the duration of torrefaction had substantial effect