Академический Документы
Профессиональный Документы
Культура Документы
Fuel
journal homepage: www.elsevier.com/locate/fuel
h i g h l i g h t s
Analysis of a technical and economic feasibility of a CTL plant with CCS.
The analysis evaluates different scenarios using Aspen Plus software.
CTL investment results in good economic performance for growing crude oil prices.
With oil price near to $98/bbl is possible to reach IRR value close to 20%.
For $28/tCO2 allowance price CCS becomes less costly than paying all CO2 emitted.
a r t i c l e
i n f o
Article history:
Received 1 September 2012
Received in revised form 14 March 2013
Accepted 1 May 2013
Available online 10 June 2013
Keywords:
Coal to liquids
Carbon capture and storage
CO2
a b s t r a c t
This paper analyzes the technical and economic feasibility of the integration of FischerTropsch process
based Coal to Liquid (CTL) plants with Carbon Capture and Storage Technologies (CCS). CTL plants could
be multipurpose, and for this reason, starting from coal can produce different energy products like liquid
fuels, such as diesel and gasoline, chemicals, electricity and hydrogen. Different plant congurations are
possible especially in the case of integration with CCS technologies. Obviously, the choice of the optimal
process conguration is one that better meets technical and economical requirements. In order to make a
rst assessment, a screening of suitable technologies has been made. The CTL facility study here proposed
is based on commercial coal gasication and FischerTropsch technologies. The system conguration
selected and the plant performance has been evaluated using Aspen Plus software. The plant size considered is about 10,000 bbl/d of liquid fuel products, equivalent to a consumption of about 4500 ton/d of coal
fed to the gasication island. The declared objective is to evaluate the potential of the identied plant and
to perform a rst economic evaluation. The ultimate goal is to determine the specic cost of produced
liquid fuels and to evaluate the economic performance of the system. The economic analysis was done
to estimate the Internal Rate of Return (IRR), the payback period and the net present value for congurations with CCS or without CO2 capture. Results shows that the CCS introduction in CTL plants has a
lighter impact on plant costs and performance since CO2 capture it is already included in the base plant.
2013 Elsevier Ltd. All rights reserved.
1. Introduction
Currently, there is considerable interest in coal conversion
technologies, also dened by the acronym CTL. In fact, their
use, in particular in countries with large coal resources, such as
China, United States, South Africa and India, enables to reduce
dependence on oil prices by replacing conventional fuels with
fuels derived from coal.
A crisis of availability of oil and an increase in its price can open
up a renewed interest in coal and its conversion to liquid fuels. CTL
technologies refer to different processes. Starting from CO and H2
851
Nomenclature
g
a
efciency
chain growth probability
Wn
1.1. Objectives
The main objective of this work is to evaluate the technical and
economic feasibility of a Sulcis Coal fed CTL plant also implemented with Carbon Capture and Storage Technologies (CCS).
The choice of the process conguration is the one that better meets
technical and economical requirements. In order to make a rst
step analysis, a suitable technology was proposed. The CTL facility
studied is based on commercial coal gasication and FischerTropsch technologies currently in use worldwide [12]. A general
scheme of the main blocks of the CTL process and possible variation is shown in Fig. 1.
Therefore, while CTL plants are considered commercial, best
practices for the use of new technologies have yet to be ascertained
and signicant improvements can be realized during systems
integration.
Another important aim of the work is the integration, within
the identied conguration, of the different sections of the plant
through the adoption of solutions that ensure the highest values
air
air
CO2
to vent
CO2
to storage
ASU
O2
CO2
COMPRESSION
ASU
raw
syngas
O2
AGR
GASIFIER
raw
syngas
FT product
FT REACTOR
coal
Tail gas
O2
ATR
FT product
AGR
GASIFIER
FT REACTOR
coal
Tail gas
REFINING
O2
ATR
REFINING
naphtha
CO2
to vent
naphtha
CO2
to vent
diesel
BOILER
diesel
POWER
BLOCK
BOILER
coal
CO2
to vent
CO2
to vent
POWER
BLOCK
coal
Electric
Power
steam
Electric
Power
steam
852
In both cases the conguration considers recycling of unconverted gas in the FischerTropsch synthesis reactor to maximize
the liquid fuel production. The recycle system is the focus of the
most current FischerTropsch commercial technologies [4]. Therefore a co-production conguration was analyzed in this study. CTL
plants are capital intensive and for small scale facilities the revenue
generated by electricity sold to the grid can charge part of the costs
decreasing the specic cost of liquid fuel product. Obviously, the
economic performance of a co-production plant depends on the local selling price of electricity. As a rst step approach we studied a
conguration that provides 50% of tail gas recirculation in order to
cover electric auxiliaries and sell the energy surplus to the grid.
3. System modeling methodology and results
Mass and energy balances give the basic information needed to
estimate the cost of the most relevant plant sections. Particular
attention was paid to the heat integration between the plant sections to improve thermal efciency. To evaluate the performance
of a chosen conguration, one general ow sheet was built in Aspen Plus. A brief description of the major equipment included in
the facility design and the Aspen Plus assumptions used in modeling follows.
3.1. Gasication section
Coal is prepared by milling, grinding and drying operations. The
solid fuel is fed to the gasier where its reacts with steam and oxygen to generate a syngas, mainly constituted by CO, H2 and CO2.
Different gasication technologies are available and the reactor
types can be grouped into three categories: moving-bed, uidbed and entrained-ow gasiers [5]. The biggest operators for
the large-scale production of liquids from coal currently use moving bed units [1]. Consequently, a FDBD Fixed Bed Dry Bottom type
has been chosen for the studied facility.
The advantage of this type of gasiers is particularly suitable for
bituminous coals that have a high content of volatile compounds
and high ash-melting point. The majority of commercial FDBD gasiers operate at pressures in the range of 2530 bar. Fixed and
moving bed gasiers require low amounts of oxygen because of
the high energy efciency of the reactor. They require, however,
a signicant amount of steam in order to moderate the temperature. Part of the steam is generated by the gasier water jacket.
Normally, such a cooling system allows the production of about
10% of the steam required for the process.
The gasier system has not been modeled in detail. Estimates of
gas composition is base on experience gained into our pilot plants,
while performance and utilities consumption have been taken
from literature [5]. Table 1 summarizes the assumptions adopted
Table 1
Assuming operating condition and syngas composition of the gasier.
Feed components per 1000 Nm3 of syngas (CO + H2)
Type of coal
Coal (kg)
Steam (kg)
Oxygen (Nm3)
Bituminous/Sulcis
750
1930
280
for gasier and syngas composition fed to the gas cleanup section.
The gasication section is equipped with a cryogenic Air Separation Unit (ASU) which provides a ow of high purity oxygen consuming about 175 kWhe/ton O2 with a purity of 94.3% (mol.) [6].
3.2. Cleanup section
The syngas produced by the gasication contains a number of
impurities, including particulates and sulfur compounds (particularly, H2S and COS) for this reason a gas cleaning section is strictly
necessary. The particulate matter is removed by ltration, despite
tar and other impurities dropped down by water scrubbing. CO2
and sulfur compounds are removed by acid gas removal system.
CO2 removal is required in order to accomplish the new European
directives (2009/29/CE) and to improve kinetic aspects of the
downstream synthesis process. In fact CO2 is no reactant in the
FT reaction (assuming no shift reaction) but its presence negatively
inuences the C5+ selectivity. Experimental studies conrm that
when the feed gas to the synthesis reactor consisted mainly of
CO2 and H2 over Co catalysts methane was the main product
(Dry, 2004).
H2S removal is required to avoid the poisoning of the synthesis
catalyst. The gas cleaning requirements are more stringent than
those used in IGCC plants and generally stay in the range of 0.2
1 ppm (Dry,1981) as maximum sulfur content. The syngas cleanup
is one of the crucial portions of the process. Among the CO2 and
H2S removal technologies Selexol has been chosen as the most
suitable technology for maturity and reliability with more than
30 years of experience and 55 operating plants installed
worldwide.
The Selexol is a physical solvent with lower solvent loss, higher
selectivity toward H2S, better thermal stability, better water solubility, and lower circulation rate [7]. The acid gas reduction was
accomplished by using a two-stage process for selective removal
of H2S (rst stage) and CO2 (second stage) from the syngas using
a dimethylether of polyethylene glycol (DMPEG). This section
was modeled using PC-SAFT equation of state model.
The process and the ow sheet were designed to take advantage
of the solubility difference of H2S and CO2 in Selexol. The main design parameters were set to meet a CO2 removal efciency of up to
88% and a 0.21 ppm maximum H2S content in the clean syngas.
The chosen pressure design was 30 bar. The CO2 removal efciency
in the AGR section has been set in order to have a lower concentration of 1.5% vol. of CO2 in the clean gas.
The Selexol ow scheme is given in Fig. 2. Most of the H2S in the
syngas is absorbed in the H2S absorber (AB1) where the gas meets
a CO2 rich solvent. The rich solvent is sent to the stripping column
and the H2S is stripped off. The reboiler duty has been calculated in
order to meet the design specication of 1 ppm H2S in the lean solvent [8]. The gas from the top of AB1 is sent to the CO2 absorber
(AB2). The CO2 rich solvent, from the bottom of the second absorber is regenerated by carrying out multiple ashes which reduce
pressure to recover the CO2 and partially recirculated it back to
the H2S absorber.
The H2S delivered in the stripping is suitable for feeding a Claustype unit used for sulfur recovery. Additional zinc oxide bed lters
are considered properly used in H2S removal for up to 0.1 ppm. In
the base case the CO2 separated is vented to the atmosphere while
in the CCS case it is sent to the compression section for nal underground sequestration.
3.3. CO2 compression section (only for CCS case)
The CO2 stream coming out from the acid gas removal section is
strongly pressurized in order to be transported to storage. Best
practices indicate pressure values close to 100 bar.
853
GAS CLEAN
MAKE-UP
AB2
CO2 HP
CO2 MP
CO2 LP
AB1
H2S
GAS IN
ST1
Generally, the necessary conditions for the transport and storage of CO2 can be reached through multi-stage intercooled compressors with condensate drain.
Normally, it is necessary to remove the water content below
500 ppm in order to avoid corrosion of the pipeline transport of
CO2, as well as the formation of hydrates that can occlude pipes
and nozzles.
In this study the CO2 delivery conditions and compression process are dened following the specic temperature and pressure
outlined in the European Best Practice assessment guidelines for
CO2 capture technologies [9]. The best operating conditions were
identied in order to obtain a concentrated current of CO2 suitable
for storage (95% by volume with H2S values <200 ppm). Fig. 3 demonstrates the section scheme. The compression pressure of 80 bar
is realized by three compression stages.
Each compression stage is followed by a phase of inter-refrigeration for which 28 C is the exit temperature of the compressor and
subsequent separation of the condensed water by ash. The liquid
portion, constituted mainly of water and therefore incondensable,
is separated and sent to treatment. At the last stage outlet the liquid stream of CO2 is pumped from 80 bar to 150 bar and subsequently cooled to 25 C. The process design assumptions of the
Aspen Plus simulation were taken from literature [9].
3.4. FT section
The FT process can be realized in different reactor types: MultiTubular Fixed Bed (ARGE), Circulating Fluidized Bed (Synthol),
Fixed Fluidized Bed (SASOL Advanced Synthol) and Fixed Slurry
Bed. According to many authors the xed bed reactor and the slurry bed reactor are the most promising [10]. Heat removal and temperature control are the central design features required to provide
the desired hydrocarbon selectivity and catalyst life. The conversion extent in the FT reactor depends on the catalyst type, temperature (LTFT process or HTFT process), reactor size and technology.
In this study a low temperature (LTFT) reactor type, operating at
250 C and 25 bar has been used, with a slurry bed design and cobalt based catalyst.
The FT conversion section is the heart of the plant. Its accurate
design is crucial in order to maximize the yield of liquid products
to make the plant economically competitive.
Fig. 4 shows the Fischer Tropsch section. The product stream
exiting from the FT reactor (R-301) is constituted mainly by water,
hydrocarbons in liquid phase (C5+) and tail gas. The stream is
cooled and the hydrocarbon liquids are separated from the tail
gas and water. Finally, the C5+ liquid products are sent to the rening process to produce commercial product.
IMPURITIES
CO2 HP
CO2 MP
CO2 LP
K-203
K-204
K-205
P-204
CO2 LIQUID
H2O
Fig. 3. PFD CO2 compression section CCS case.
854
Wn=n 1 a2 an1
-1.5
log (Wn/n)
The tail gas from the FT section is partly recycled to the reactor
for additional conversion and partly sent to power generation
block. The recycled gas passes through an autothermal reformer
(block R-302) where the C1C4 fraction is converted to CO and
H2. The Fischer Tropsch synthesis is strongly exothermic. The surplus heat is used to produce superheated steam at 20 bar which is
fed to the steam turbine to generate power. A small quantity of H2
required for the upgrading process is separated by tail gas with a
PSA system.
The FT synthesis is a carbon chain building process, where
CH2 groups are attached in a carbon chain. The resulting overall
reaction can be presented as:
-2
-2.5
-3
-3.5
0
10
15
20
25
30
35
n
Fig. 5. Product distribution following ASF, a1 = 0.85 and a2 = 0.92.
Signicant deviations from the AndersonSchulzFlory distribution are reported in the literature [11], therefore we can observe
a double alpha effect for both iron and for cobalt catalysts. The
double alpha values used in this study are: a1 = 0.85 for C1C16
carbon class and a2 = 0.92 for C17C32 [11]. Eq. (2) is shown in
Fig. 5. The total CO conversion in the FT reactor is 80%. The C20
C32 hydrocarbon components were incorporated in the weight
fractions of C20. All components C32+, with more than thirtytwo C atoms, were included in weight fractions of C32 [12]. Table 2
[13] gives the alkene to alkane ratios for several carbon number
products obtained in a slurry reactor over Cobalt catalysts used
in the yield calculation to predict the alkenes formation.
Table 2
Ratios 1-alkene/n-alkane.
Carbon
number
Ratios 1-alkene/
n-alkane
C2
C3
C4
C5
C6
C10
C15
0.05
1.4
1.4
1
1
0.9
0.4
855
where GFT is the mass ow rate kg/s of liquid product and Gcoal is the
mass ow rate kg/s of coal input.
The reported thermal efciency is calculated as a ratio between
the lower heating value of the primary liquid hydrocarbon products plus the net plant power and the lower heating value of the
coal feed. Results show that more than 47% of input energy can
be converted to FT products and electric energy. In the base case
the energy content of the liquid fuels is 40% of the energy content
BASE CASE
CO2 out
7678 t/d
Coalgasification
Coal
4500 t/d
FT LiquidsProduction
FT liquids
8530 bbl/d
Export Power
90 MWe
Ash
431 t/d
CCS CASE
This represents the increase in plant energy input per unit of liquid products and net electrical output [15]. The EP under the
assumptions in this study is 2.7%, in comparison to the EP value
of about 12% for an IGCC plant equipped with CCS [16]. Therefore,
the coal required to produce the same amount of electricity in IGCC
with CCS is higher than the coal required in a CTL for CO2 capture
plant. In fact, IGCC plants without CCS use a different conguration
from ones with CCS. In a power generation plant the major part of
CO2 energy penalty and capture cost is associated with the creation
of a concentrated CO2 stream ready to be stored. The water gas
shift and CO2 separation equipment has to be added in a IGCC
plant. On the contrary, in a CTL plant CO2 capture it is already included in the base plant process [17]. The CCS penalty is much
smaller than an IGCC plant. In the CTL facility studied, in order to
capture all the CO2 emitted from the plant, it is necessary to add
an amine-based (MEA) chemical absorption section that operates
the removal of CO2 emitted from boiler and power sections.
Table 3 shows the overall efciency for both plant congurations, in agreement with the results reported by the literature for
similar plant [4].
4.2. Plant mass balance
The plant is fed with 4500 ton/d of coal consisting of a blend of
60% of Sulcis coal and 40% of import bituminous coal. The gasier is
fed with 4000 ton/d of coal, 20 kg/s of O2 and 93 kg/s of steam at
30 bar. An auxiliary boiler fed with 500 ton/d of coal provides part
of the steam supplied to gasier strictly necessary in the startup
phase.
4.2.1. Cleanup section result
The cleanup section processes 100 kg/s of gas and removes the
content of H2S down to 1 ppm. In the conguration with CCS the
CO2 is captured at 88% efciency in the AGR section and then sent
to the compression section. The electricity load of the AGR section
is essentially related to the gas recirculation compressors and to
solvent pumps. The specic energy expenditure in the stripper
reboiler is 3.7 MJ/kg H2S. The overall energy expenditure of the
cleanup is 435 kJ/kg of coal. The compression and liquefaction
Table 3
Summary of overall plant data.
Coal
LHV coal
Thermal input
Gasoline C5C11
Diesel C12C32
LHV FTa
Capacity factor
Output
Net plant power
Electric production
Total efciency (LHV basis)
Total FT efciency (LHV basis)
CO2 capture (%)
CO2 captured
5054 t/d
CO2 out
2624 t/d
Coalgasification
Coal
4500 t/d
FT LiquidsProduction
FT liquids
8530 bbl/d
Export Power
74 MWe
Ash
431 t/d
Fig. 6. simplied schematic of the plant input and outputs.
ton/d
MJ/kg
MWth
bbl/d
bbl/d
MJ/kg
%
MWth
MWe
MWhe/y
Base case
CCS
4447
25
1287
3240
5290
44
85
512
90
671,056
0.47
0.40
0
4447
25
1287
3240
5290
44
85
512
74
553,100
0.46
0.40
66
The assumed FT LHV is set equal to the one in Steynberg studies [14].
856
Table 4
Assumptions and results relative to the calculation of the TOC.
Parameter
BEC
Engg CM H.O. & Fee
EPCC
Project Contingency
Process Contingency
TPC
Start up
Owners Costs
Assumptions
10% BEC
20% BEC
25% BEC FT section
2% EPCC
8% TPC
TOC
Base case
CCS case
M$
M$
M$
M$
M$
M$
M$
M$
567
45
612
113
15
741
12
59
579
46
625
116
15
756
12
60
M$
812
829
pressure which produces a rich CO2 stream with less energy penalty. In the CCS case about 1.57 million tons of CO2 per year are
captured and stored while 0.81 million are emitted.
Global results show 66% of the CO2 captured is vented in the
base case or sent to storage in the CCS case. To improve this performance an additional capture section can be installed downstream
of the auxiliary boiler where CO2 is at atmospheric pressure and
at concentration is close to 13%. In the case of nearby Zero Emission
approach the combined cycle exhaust can also be treated with a
post combustion capture section with higher expenditures in
terms of energy and investment costs.
Looking at the carbon ows in the CCS case, 2744 tons/d of carbon contained in coal is divided as follows: 51% is captured and
stored as CO2, 26% is vented in the exhaust gas as CO2, 22% is transferred to liquid fuels and released as CO2 during its use and the
remaining 1% is discharged from the plant with ashes.
5. Economic analysis
This study evaluates the performance and cost of different CTL
plant congurations in order to propose possible investments.
The plant congurations evaluated in this study focus on the optimal production of liquid fuels and electric energy while simultaneously reducing CO2 emissions. In this study, two CTL plant
congurations were compared in order to assess the economic impact on the addition of CCS.
5.1. Economic analysis assumptions
The method for estimating total plant cost and total plant
investment was developed using a DOE methodology [20]. The
TOC Total Overnight Capital cost has been estimated as the sum
of the TPC (Total Plant Cost) plus all other overnight costs, including owner costs. The TPC is calculated by the Engineering, Procurement and Construction Cost (EPCC), that comprises the BEC (Bare
Erected Cost) in addition to the cost of services provided by the
engineering, procurement and construction contractor costs, plus
project and process contingencies. Table 4 shows the assumptions
used for the calculation of the Total Overnight Capital cost as well
as the results obtained for the two congurations. Assumptions include a 25% process contingency applied to the FT section in order
to reect the lesser technological maturity of the FT liquids
equipment.
The BEC has been calculated using the factored estimation
method based on known costs for major equipment as found in
the literature.
The study provides the basis for estimating global CO2 emissions associated with coal conversion in power and FT fuels. CO2
is emitted by the acid gas removal section, by the auxiliary boiler
and by the power section. The CO2 capture is applied downstream
of the gasier. Consequently, the capture takes place at a high
where Co is the base cost for each component by size, while C is the
cost of the component at the required size S, and f is the cost scaling
factor.
Table 5 gives the base costs and cost scaling factors used for the
BEC estimate. The notes given with the table describe the sources
C20+
12%
C char
C1-4
18%
C exhaust gases
C liquid product
C storage
0%
20%
40%
60%
C17-C20
29%
C5-C16
41%
857
Base scale
Base cost M$
Scale factor
Size plant
Cost M$
BEC $2010
So
Co
Base case
CCS case
105
210
91
60
9,5
78
14
22
25
35
0.5
0.67
0.67
0.67
0.67
0.67
0.75
0.67
0.67
0.67
105
45
114
66
11
53
28
9
24
36
110.6
48.3
162.5
70
0
59.6
39
10
27
40
110.6
48.3
162.5
70
12
59.6
39
10
27
40
567
579
ASU and Oxidant Compression and CO2 compression to supercritical outlet pressure are as indicated by: FischerTropsch Fuels from Coal and Biomass Thomas G. Kreutz,
Eric D. Larson, Guangjian Liu, Robert H. Williams Princeton Environmental Institute Princeton University Prepared for 25th Annual International Pittsburgh Coal Conference
29 September2 October, 2008 Pittsburgh, Pennsylvania, USA.
b
Selexol double and single stage CO2 removal and pulverised coal boiler are based on: Cost and Performance Baseline for Fossil Energy Plants DOE/NETL-2007/1281.
c
Gasier & accessories are base on: British Gas/Lurgi Gasier IGCC Base Cases PED-IGCC-98-004, September 1998, Latest Revision June 2000 NETL.
d
Source: Technical and Economic Assessment of Small-Scale FischerTropsch Liquids Facilities DOE/NETL-2007/1253.
e
BOP Balance of Plant include: accessory electric plant, instrumentation & control, improvements to site, buildings & structures.
BOP 12%
ASU 20%
ASU 19%
BOP 12%
Power
generation
section 8%
Power
generation
section 9%
FT section
10%
FT section
10%
CO2
compression
0%
Gasifier &
boiler 37%
AGR 12%
base case
Gasifier &
boiler 36%
CO2
compression
2%
AGR 12%
CCS case
Table 6
Financial analysis parameters assumptions for base scenario.
Parameter/assumption
Value
Construction period
Incurred capital in: year 1
Year 2
Year 3
Debt equity ratio
Capacity factor
Plant lifetime
Interest rate
Tax rate
Loan interest rate
Annual O&M expenses
Coal ratio Sulcis/import coal
Sulcis coal price
Bituminous coal price
CO2 transport and storage cost
Electricity price
3 years
10%
60%
30%
55:45
85%
30 years
8%
28%
8%
5.2% TCP
60%
$50/ton
$100/ton
$8/ton
$115/MWh
The results coming from the analysis are the Internal Rate of Return (IRR), the discounted cash ow and the payback time. These
values provide information in order to identify the parameters that
most affect the investment.
Table 8
Cost of liquid product on base scenario.
Compositions of the production costs M$/y
Fuel costs
Operating & maintenance
Capital costs
CO2 capture cost
113
32.75
33.74
0
113
33.41
34.42
11.47
179.06
68
13
191.87
73
14
100
858
95
90
CCS case
80
75
70
65
60
55
50
base case
85
10
20
30
22
Table 7
Economic analysis results base scenario.
Base case
CCS case
8530
812
122.5
20
7
1024
8530
829
133.75
15.7
9.6
669
20
IRR (%)
18
base case
16
CCS case
14
12
10
8
0
10
20
30
Table 9
Effect of CO2 allowance price on the main economic parameters.
Parameter
NPV (M$)
Base case
CCS case
Base case
CCS case
0
10
20
30
1014
764
515
265
669
552
435
318
7
8.5
11.5
15.8
7
8.50
11.5
15.8
impact strongly the IRR. For a FT fuels selling price of $74/bbl both
investments have negative NPV. The analysis shows clearly that
CTL plants are protability under high crude oil prices.
The increase of the TOC was also found to strongly impact the
nancial performance, in fact, as shown in Fig. 12 and Table 10,
by applying +50% on TOC cost the IRR is considerably lowered in
both cases. Twice the TOC cost produces negative NPV and IRR less
than the interest rate.
859
35
IRR (%)
30
base case
25
20
CCS case
15
10
5
0
35
30
IRR (%)
25
base case
20
CCS case
competitive. The poly-generation of power and liquid fuels can improve plant exibility in order to better satisfy the energy market
demand. The best solution from the economic point of view is
achieved when the plant is located close to the extraction site of
coal. In fact, mine mouth plant installation reduces transport costs
and takes advantage of the reduction in coal supply costs.
Specically, the analysis results show that a 4500 ton/d of coal
(1287 MWth) can produce 8530 bbl/d (2.6 Mbbl/y) of liquid fuels
and 90 MWe emitting 2.37 Mton/y of CO2. Carbon sequestering
can reduce this quantity up to 0.8 Mton/y decreasing the power
output to 74 MWe due to the drop of 66% in CO2 emissions. In both
cases global efciency is about 47%.
CTL plants equipped with CCS become competitive with a FT
fuels selling price of $134/bbl. The sensitivity analysis indicates
that CSS competitiveness depends on the applied price of CO2
allowance. The $28/tCO2 CCS allowance price becomes less costly
than paying all CO2 emitted. Finally, the analysis shows clearly that
CTL plants are protability under high crude oil prices and the
cost-effectiveness depends strictly on the FT fuels selling price.
Future work will expand the technical and economic feasibility
analysis by varying the specic ratio of poly-generation capabilities of the plant, the plant scale and the CCS capture conguration.
Acronyms
15
10
5
0
95000 105000 115000 125000 135000 145000
Table 10
Effect of TOC on the main economic parameters.
Base scenario
+50% TOC
Specic capital
cost $/bbl/d
IRR base
case
$/bbl/d
IRR CCS
case
95,214
143,031
20
10.5
97,134
149,726
15.7
7.2
6. Conclusions
The main objective of this paper is to evaluate the technical and
economic feasibility of a CTL plant and its implementation of carbon capture and storage technologies. This analysis was developed
under the recent European legal framework in order to propose an
assessment on the feasibility and convenience to realize a plant
CTL with or without CCS. In particular, this analysis is addressed
to countries dependent on oil imports but with local coal resources. The analysis evaluates different scenarios in order to
underline CTL potential benets in the Italian energy market. This
analysis indicates a powerful synergism among poly-generation
CTL systems and CO2 capture systems.
The CTL investment option results in good economic performance in the case of increasing crude oil prices. As a matter of fact,
at crude oil price levels of $98/bbl could possibly reach a return
investment of close to 20% with a FT fuels selling price of $122.5/
bbl and a specic barrel production costs close to $70/bbl. The
CCS introduction in CTL plants has a lighter impact on plant costs
and performance with respect to power production plants, since
CO2 capture it is already included in the base plant. In the case of
a CO2 allowance price over $28/ton this option becomes the most
AGR
ASF
ASTM
ASU
ATR
BEC
CCS
CCT
CEPCI
CTL
DOE
EPCC
FT
GSE
HRSG
HTFT
ICL
IEA
IRR
LHV
LTFT
MIT
NETL
PFD
TOC
TPC
Acknowledgments
This work was developed into the RdS Research Program on
Electrical Grid funded by the Italian Ministry of Sustainable Economic Development.
References
[1] Couch Gordon R. Coal to Liquids. IEA Clean Coal Centre; 2008.
[2] Tijmensena Michiel JA, Faaija Andr PC, Hamelincka Carlo N, van Hardevel
Martijn RM. Exploration of the possibilities for production of Fischer Tropsch
860
[3]
[4]
[5]
[6]
[7]
[8]
[9]
[10]
[11]
[12] Hamelinck Carlo N, Faaij Andr PC, den Uil Herman, Boerrigter Harold.
Production of FT transportation fuels from biomass; technical options, process
analysis
and
optimisation,
and
development
potential.
Energy
2004;29:174371.
[13] Dry ME. Chemical concepts used for engineering purposes. Studies in Surface
Science and Catalysis 2004;152:196257 (Elsevier, Chapter 3).
[14] Steynberg Andre P, Nel Herman G. Clean coal conversion options using
FischerTropsch technology. Fuel 2004;83:76570.
[15] Chen C, Rubin ES. CO2 control technology effects on IGCC plant performance
and cost. Energy Policy 2009;37:91524 (Elsevier).
[16] Ordorica-Garcia G et al. Technoeconomic evaluation of IGCC power plants for
CO2 avoidance. Energy Conversion and Management 2006;47:22509
(Elsevier).
[17] Mantripragada H, Rubin E. Techno-economic evaluation of coal-to-liquids
(CTL) plants with carbon capture and sequestration. Energy Policy
2011;39(5):280816.
[18] Borg et al. Effect of biomass-derived synthesis gas impurity elements on
cobalt FischerTropsch catalyst performance including in situ sulphur and
nitrogen addition. Journal of Catalysis 2011;279:16373 (Elsevier).
[19] Technical and Economic Assessment of Small-Scale FischerTropsch Liquids
Facilities, DOE/NETL-2007/1253.
[20] Quality Guidelines for Energy Systems Studies Cost Estimation Methodology
for NETL Assessments of Power Plant Performance, DOE/NETL-2010/1455.
[21] Mc Kinsey Report, Carbon Capture & Storage: Assessing the Economics, 2008.