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Wood Residue to Energy Conversion

Wood residues come from various sources like forest operations, pulp industry, sawmilling, and plywood production. They represent an important source of biomass for energy but are scattered. Thermal processes like combustion, gasification, pyrolysis and liquefaction can convert wood residues into useful energy products. Pyrolysis is the key reaction that occurs in all these thermal processes, breaking wood down into char, gases and oils at high temperatures without oxygen. The operating conditions of each process, like temperature and atmosphere, determine the yields and properties of the resulting products.

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Ayushi Garkoti
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0% found this document useful (0 votes)
193 views25 pages

Wood Residue to Energy Conversion

Wood residues come from various sources like forest operations, pulp industry, sawmilling, and plywood production. They represent an important source of biomass for energy but are scattered. Thermal processes like combustion, gasification, pyrolysis and liquefaction can convert wood residues into useful energy products. Pyrolysis is the key reaction that occurs in all these thermal processes, breaking wood down into char, gases and oils at high temperatures without oxygen. The operating conditions of each process, like temperature and atmosphere, determine the yields and properties of the resulting products.

Uploaded by

Ayushi Garkoti
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PPT, PDF, TXT or read online on Scribd

Wood Residues

Source of Residue Type of Residue


Forest operations Branches, needles, leaves, stumps, roots,
low grade and decayed wood, slashings and
sawdust
Pulp industry, Sawmilling Bark, sawdust, trimmings, split wood,
and planning planer shavings
Plywood production Bark, core, sawdust, veneer clippings and
waste, panel trim, sanderdust
Particleboard production Bark, screening fines, panel trim, sawdust,
sanderdust
Wood Wastes Packing material, old wooden furniture,
wooden building waste (demolition wood)
Estimated potential of Wood Residues
in the World

 Overall quantity of WR ~ 2,000 MT/y or ~


650 MTOE/y to compare with
 7,000 MT/y of Forest biomass or 2 230
MTOE/y
 WR ~ 30% of potential Forest Biomass
Wood Residues vs “Clean Wood”

 Overall quantity of WR: 16 MT / year to compare with


o ~ 23 MT / Year of processed wood (5 MT/y imported)
o ~ 40 MT / Year of Wood biologically produced by the
forest
o ~ 20 MT / Year of Fuel Wood (estimated) with 80%
domestic consumption
 WR represent an important source of Biomass (5.5
MTOE)…but is scattered!
 WR corresponds only to 6% of the oil consumption (96
MT/y)
Biomass upgrading into Energy or Chemicals

Co-combustion
Electricity
Heat

Direct
Biomass
Combustion
Fuel cells SNG
DME
H2
Gasification Engine
Pyrolysis Turbine Fischer Tropsch
hydrocarbons
Alcohols
Direct N/A ? Methanol
Liquefaction Ethanol

Bio-fuel
Bioprocesses N/A ?
Overview of “Wood thermal Processes”
Wood

(Co) combustion Direct Liquefaction Pyrolysis Gasification

slow Atmospheric or pressurized


H2O, critical conditions, fast, flash O2, air, H2O
Hydro liquefaction (H2)
High Pressure
Flue gas char Direct Indirect
Liquid biomass oil heating Heating
Heavy bio-oil gas
syngas
Upgrading treatment

Engine or Turbine Synthesis/cleaning

Heat and Electricity Bio-fuels Charcoal


CH3OH, CnHm, H2
Operating conditions of the thermal processes
Thermal Process Temperature Atmosphere Products Mean
overall
Yield
Combustion > 900°C O2 (air) CO2 + H2O + N2 ~ 65 %
+ ashes to be treated
Pyrolysis < 500°C Inert gas or char + tars + gas, which ~ 45 %
Low pressure proportions are related to
the pyrolysis parameters

Gasification by > 700°C Inert gas or Mainly gas (CO, H2, CH4, ~ 75 %
Fast pyrolysis Low pressure C2H4 …) with low quantity of
char used
Gasification > 800°C Air or H2O Gas (H2, CO, CO2, CH4, N2) 50-60 %
vapour + ashes to be treated

Liquefaction by < 550°C Low pressure High viscosity liquid (phenols) ~ 75 %


Fast Pyrolysis

Direct 300°C- 350°C CO High High viscosity liquid (phenols) ~ 80 %


Liquefaction Slurry in water pressure non soluble in water
Pyrolysis is the Key Reaction of
all the thermal Processes

WOOD

Cutting or Grinding

Drying

Pyrolysis

Combustion Gasification Liquefaction Charcoal making Heated Wood


Mechanism of the pyrolysis
P rim a ry d e g ra d a tio n S e c o n d a ry d e g ra d a tio n
a c id s , a c e to l,
C h a r, H 2 O ,
fu rfu ra l, la c to n s ,
CO ,CO 2
h yd ro xya c e ta ld e h yd e
fra g m e n ta tio n ,
d e c a rb o n yla tio n (C O ),
lo w T h ig h T d e h yd ra tio n (H 2 O )
H O LO C E LLU LO S E
d e p o lym e riza tio n S e c o n d a ry
d e g ra d a tio n
tra n s g lic o s ila tio n
le vo g lu c o s a n
a n d s u g a rs

S e c o n d a ry
h ig h T d e g ra d a tio n
p h e n o ls , C a rb o n yl
L IG N IN m e th o xyp h e n o ls (g u a ia c o ls ), c o m p o u n d s,
d im e th o xyp h e n o ls (s yrin g o ls ) fu ra n s , p h e n o ls ,
lo w T d e p o lym e riza tio n CO ,CO 2

C h a r, C O , C
O2
Operating conditions of the pyrolysis process

PAH

PAH: Polycyclic Aromatic Hydrocarbons


To lower the PAH’s

Naphtalene, Anthracene, Pyrene, Benzopyrene ……


which are formed during the pyrolysis step of the
thermal conversion, it is compulsory:
 to decrease the Residence Time
 to increase the Temperature
 when it is possible!
1. Introduction

2. Pyrolysis

3. Gasification

4. Carbonisation

5. Liquefaction

6. Conclusion
Possible applications of the Product Gas

 co-combustion in a coal power plant


 co-combustion in a natural gas power plant without
modifications at the burners
 production of electric energy in a gas turbine
 production of electric energy in a gas engine
 production of electric energy in a fuel cell
 as synthesis gas in the chemical industry
 as reduction gas in the steel industry
 for direct reduction of iron ore
 for production of Synthetic Natural Gas by methanation
 for production of Liquid Fuels by Fischer-Tropsch
Main Reactions
 Wood (Pyrolysis) C slightly endothermic
 C + O2  CO2 (ΔH0= -391,6 kJ mol-1) exothermic
 C + H2O  CO+H2 (ΔH0 = + 131,79 kJ mol-1) endothermic
 C + CO2  2 CO (ΔH0 = + 179,3 kJ mol-1) endothermic
 CO + H2O  CO2 + H2 (ΔH0 = - 47,49 kJ mol-1) slightly
exothermic
 C + 2H2  CH4 (ΔH0= - 22 kJ mol-1) slightly exothermic

 With the operating parameters (Pressure, Temperature) it is


possible to select a gas containing more Syngas (CO+H2) or
more SNG (CH4)
Main kinds of
Reactors for
Gasification

Updraft and Downdraft


reactors have been
developed since ~ 1930.

They produce a low BTU


Gas (~ 6000 KJ/m3) with
tars.

Actually the new systems


use mainly fluidized beds
and circulating fluidized
beds….but they are often
too complicated energy
output < energy in put!
Circulating Fluidized Bed
Advantages of Gasification by fast Pyrolysis
in a Circulating Fluidized Bed System
• product gas nearly free of nitrogen
• calorific value higher than 13 MJ/Nm³
• very low tar content due to steam gasification
• gas quality is independent of water content in biomass feed
• now, the apparatus are compact……not enough!
• a wide range of feedstock can be gasified
• possibility to use a catalyst as bed material (regeneration
of catalyst in combustion zone) to influence the gas
composition and gasification kinetic in a more positive way

• But sometimes energy output < energy input!


Circulating Fluidized Beds

Numerous systems
have been developed
since 1980:
- KUNII
- FERCO
- Our (TNEE)
- RENET (Güssing)
- ………….

Example: FERCO (Battelle)


We have an old expertise in wood
gasification in dual fluidized bed
pyrolysis, until the pilot scale
A pilot with a capacity of 500Kg/H
pine barks was operating in a pulp mill
in 1984/1985.
Its power was around 2 MW
and it produces a medium BTU Gas
(HHV around 16000 KJ/m3)
fumées
(950°C)

cyclone
dépoussièreur
gaz de pyrolyse caloporteur
(850°C) (950°C) lit transporté
de combustion
(950°C)

bois

char + caloporteur

lit en pyrolyse
( ~ 800°C)
gaz de pyrolyse
recyclé (300 - 400°C)
20 Years later….always the same process developed in the
RENET Biomass Power Station, Güssing, Austria (Schematic layout)
Photos of the RENET Pilot
which start in Austria in 2001
Circulating Fluidized Bed with CO2 Absorber
Complete Syngas Process

Flue Gas Fly Ash Wet Shift CO2


removal scrubber Reactor elimination

Heat
Exchangers Gas
compression
Catalyst
heat Water treatment &
carrier steam production unit
Combustor Gasifier Synthesis
Gas
Bottom Ash
Extraction

Air
Steam Dried
Biomass
Optimum Capacity of Gasification Processes
1 kW 10 kW 100 kW 1 MW 10 MW 100 MW 1000 MW

Updraft

Downdraft

Fluidised Bed

Circulating Fluidised
Bed

Pressurised fluidised
Bed

0,2 kg/h 2 kg/h 20 kg/h 200 kg/h 2 t/h 20 t/h 200 t/h

10t/h could be a great maximum for RW


 To solve the problem of capacity, it is necessary to
have a pre-treatment process producing a char from
different kinds of biomass, which could be then
transformed at a larger scale.
 Such a system is proposed for the production of
Hydrogen from Biomass
 The Philosophy of this two step process could be
adapted, as the optimum input feed of the
gasification must be over 10T/H

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