Assessing The Feasibility of Using The Heat Demand-Outdoor Temperature Function For A Long-Term District Heat Demand Forecast
Assessing The Feasibility of Using The Heat Demand-Outdoor Temperature Function For A Long-Term District Heat Demand Forecast
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Energy Procedia 00 (2017) 000–000
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EnergyProcedia 142
Procedia 00(2017)
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9th International Conference on Applied Energy, ICAE2017, 21-24 August 2017, Cardiff, UK
Assessing
Zakir theKhanfeasibility
a,b
*, Suzana Yusup of cusing
, Prashant the heata, Ian
Kamble demand-outdoor
Watsona
temperature function for a long-term district heat demand forecast
Systems Power and Energy, School of Engineering, University of Glasgow, Glasgow, G12 8LL, UK
a
Department of Chemical Engineering, COMSATS Institute of Information Technology, Lahore, 54000, Pakistan
b
c
Centre for Biofuel and Biochemical, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, Tronoh, 31750, Perak, Malaysia
1876-6102
1876-6102 © 2017
© 2017 TheThe Authors.
Authors. Published
Published by Elsevier
by Elsevier Ltd. Ltd.
Peer-review
Peer-reviewunder responsibility
under of theof
responsibility scientific committee
the Scientific of the 9thof
Committee International Conference onSymposium
The 15th International Applied Energy.
on District Heating and Cooling.
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.
10.1016/j.egypro.2017.12.610
1578 Zakir Khan et al. / Energy Procedia 142 (2017) 1577–1581
2 Zakir Khan/ Energy Procedia 00 (2017) 000–000
costly for small scale operation [11]. However, utilizing steam has a high energy penalty; consequently, optimal experimental
conditions need to be identified to allow efficient and economical gasification operation.
The present study addresses the energy flow of ICA steam gasification in a pilot scale bubbling fluidized bed. The study investigates
the energy balances with respect to gasification temperature along with hydrogen production under the limitation of CO 2 adsorption
temperature inside the gasifier.
Nomenclature
H enthalpy
Hf formation enthalpy
∆Hi change in enthalpy of individual component
ni moles flow rate of individual component
QSteam energy associated with steam
QExt external energy (energy provide by external heater)
PKS palm kernel shell
Figure 1 shows a process diagram of pilot scale fluidized bed ICA steam gasification system.
The gasification system mainly comprises a fluidized bed reactor with external electric heaters, biomass feeding system, steam
generator and superheater, cyclone solid separator, wet scrubber, water separator, and gas analyzing system. After the gasifier,
product gas passes through the cyclone to separate solid particles from the product gas. The product gas then passes through the
scrubber and attains a temperature less than 40 °C and followed by a separator to remove any final traces of water in the product
gas stream. The gas sampling point is located at the exit of water separator. The gas analyzing system consisted of Gas
Chromatography (Teledyne 7500, Teledyne Analytical Instrument) with an Infrared (IR) type detector. Hydrogen and nitrogen
were detected by Gas Chromatography utilizing a Molecular Sieve.
The energy balance over the fluidized bed gasifier is shown in Figure 2 and is carried out using Equation (1).
N M
(H
i 1
PKS H H 2 0 Qsteam QExt ) ( H H 2 H CO H CO2 H CH4 H unreactedsteam )
e 1
(1)
Generally, H is calculated based on the heat of formation or formation enthalpy represented as Hf. The enthalpy of each
component is calculated using Equation (2).
Zakir Khan et al. / Energy Procedia 142 (2017) 1577–1581 1579
Zakir Khan/ Energy Procedia 00 (2017) 000–000 3
H i ni ( H f (i ) H i ) (2)
This can be further elaborated in terms of specific capacity, Cp, along with initial T1 and T2 final temperatures. ∆Hi is then
calculated using Equation (3).
T2
H i C p dT (3)
T1
The values for Hf and Cp are given in Appendix A. The energy balance was carried out using eSankey 2.x software.
Fig. 2. Energy balance of integrated catalytic adsorption (ICA) steam gasification of palm kernel shell
From the energy analysis of the energy inputs into the gasifier, it was found that the energy required for gasification increased
from 3.64 to 4.74 kW with an increase gasifier temperature from 600°C to 750°C. The analysis clearly indicates that the required
energy increases due to the endothermic nature of the process. Generally, the energy is utilized to heat up the injected steam to the
desired reactor temperature, biomass decomposition and associated endothermic reactions i.e. char gasification and methane
reforming. As the temperature of the gasifier increases, the energy requirements increase inside the reactor. This increasing energy
consumption enhances the product gas yield via endothermic reactions which corresponds to higher energy released in the outlet
stream, as shown in Figures 3 and 4. Similarly, high activity of endothermic reactions increase the steam consumption inside the
reactor which reduces the energy associated with unreacted steam at the exit of the fluidized bed gasifier. A major part of the
energy is released as unreacted steam in the process which can be optimized through heat integration. The increase of external
energy requirements with increasing gasification temperature was also observed by Franco et al. [10] for biomass steam gasification
in fluidized bed gasifier.
Figure 5 shows the product gas composition with the gasification energy required at 600 °C, 675 C° and 750 °C. The energy
required first decreased from 600 °C to 675 °C (3.64 kW to 3.41 kW) and then increased at 750 °C (4.74 kW). This may be due to
the highly active CO2 adsorption reaction at 675 °C which can also be verified by maximum H 2 with zero CO2 concentration. The
exothermic nature of the CO2 adsorption reaction provides heat for endothermic gasification reactions and reduces the overall
energy requirements for the process in the gasifier [12]. Besides, H2 yield increases with increasing gasification energy and the
maximum yield were observed at 750 °C. At high temperature, biomass to gaseous conversion is high and the individual gas
component flow rates are higher compared to that at lower temperatures. High temperatures favour endothermic reactions i.e.
methane reforming which forms three hydrogen molecules for each methane molecule consumed. This can also be justified by
lower methane concentration at high temperature (750 °C). Tar cracking is also an endothermic reaction and may contribute to an
increase in hydrogen content in the product gas [13].
Fig. 5. Effect of temperature on product gas composition and required gasification energy at steam to biomass ratio of 1.5 (wt/wt), catalyst to biomass ratio of 0.1
(wt/wt) and fluidization velocity of 0.21 m/s
4. Conclusions
Steam is found to be the most promising gasification agent for hydrogen production as compared to air or pure oxygen. However,
steam brings a high energy plenty to the process in terms of required energy for gasification. The present study showed that the
process power requirements were overall increased with increasing temperature from 675 to 750 °C, whilst a slight drop was
observed from 600 °C to 675 °C. This affect contributed to high CO2 adsorption at 675 °C which helped to reduce the energy
requirements. The unreacted steam carried away the major portion of the energy from the system, capturing and integrating this
potential heat loss improves the viability, energy efficiency and economic case for hydrogen production via gasification.
Acknowledgements
The authors gratefully acknowledge financial and technical support by Universiti Teknologi PETRONAS.
Zakir Khan/ Energy Procedia 00 (2017) 000–000 5
Appendix A.
Table 1. Enthalpy and heat capacity of components at the reference state [14, 15]
Component Hf ,(J.mol-1) Cp(J.mol-1K)
Water -241830 72.43+(10.39×10-3)T-(1.50×10-6)T2
Hydrogen 0 27.01+(3.51×10-3)T-(0.69×105)T-2
1206900 82.34+(4.97×10-2)T-(12.87×105)T-2
Calcium carbonate
x
LHV H f CO2 ( H f H 2O ) 176.67+(406.84×10-3)T-(59.82×105)T-2-(151.54×10-6 (T2)
PKS (Cellulose) 2
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