Cormos 2023
Cormos 2023
Energy
journal homepage: www.elsevier.com/locate/energy
A R T I C L E I N F O A B S T R A C T
Keywords: Biomass gasification represents an effective and promising conversion technology to different energy carriers/
Biomass gasification chemicals. Biomass gasification with CO2 capture will give an energy conversion system with negative CO2
Hydrogen emissions. This work assesses the techno-economic and environmental implications of decarbonized green
Pre-combustion CO2 capture
hydrogen generation using the biomass gasification. Several pre-combustion decarbonization technologies were
Gas-liquid absorption
Membrane
evaluated: chemical and physical scrubbing (absorption), membrane, hybrid membrane - chemical scrubbing. All
Hybrid systems evaluated biomass gasification concepts have 300 MW hydrogen output (corresponding to 100,000 Nm3/h
hydrogen with purity above 99.95% vol.) with 90% carbon capture rate. Different system engineering tools were
employed for the integrated assessment. As an important novelty outcome of this work, the green hydrogen
production from decarbonized biomass gasification has promising potential to deliver high energy conversion
efficiency (in the range of 57–59%), lower energy and cost penalties for decarbonization (about 2.2–3.5 net
points), negative carbon emissions (considering that the primary fuel - biomass - is of renewable source). Among
various assessed decarbonization technologies, the membrane system shows better techno-economic perfor
mances than the gas-liquid absorption (e.g., reduced CAPEX and OPEX by 7% and 7–9% respectively, inferior
hydrogen production cost by about 7% etc.).
https://doi.org/10.1016/j.energy.2023.126926
Received 21 November 2022; Received in revised form 6 February 2023; Accepted 8 February 2023
Available online 9 February 2023
0360-5442/© 2023 Elsevier Ltd. All rights reserved.
C.-C. Cormos Energy 270 (2023) 126926
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C.-C. Cormos Energy 270 (2023) 126926
hydrocarbon catalytic reforming in different design configurations (e.g., physical solvents can be done thermally (as for chemical ones) or pref
conventional steam reforming, autothermal reforming using oxygen or erably by pressure reduction. The physical solvents have a lower CO2
air) [24]. The gasification process is another partial oxidation technol removal selectivity as the chemical ones. Therefore, some quantities of
ogy with promising potential to become a key process for hydrogen other gases (e.g., hydrogen, nitrogen, argon) are carried out with
production [25]. One distinct advantage of gasification in comparison to captured CO2 reducing its purity. Fig. 3 presents the conceptual layout of
reforming represents its ability to process a wide variety of solid feed CO2 removal in a pre-combustion capture arrangement in which the
stocks (fossil or renewable) not only hydrocarbons (most of them of pressure reduction was used for solvent regeneration followed by gas-
fossil origin) [10]. Through the gasification process, the fuel is partially liquid separation [12].
oxidized using steam and air/oxygen to syngas. Using an oxygen-blown Application of membrane separation in a pre-combustion decar
gasifier, although implies an Air Separation Unit (ASU), it has positive bonization system is positively influenced by high pressure of shifted
effect on syngas quality and downstream purification issues. Following syngas (about 33–36 bar for a gasification system operated at 40 bar) as
gasification stage, the syngas is shifted catalytically to increase the separation driving force. As membrane separation unit, a two-stage
hydrogen production yield and to raise the CO2 partial pressure system using a hydrogen selective membrane was used [28]. Fig. 4
following its capture in an Acid Gas Removal (AGR) unit. In AGR unit, if presents the conceptual layout of pre-combustion CO2 removal using a
hydrogen sulphide (H2S) is present in relevant levels, this acid gas is also membrane unit [19].
removed (separate from CO2) and sent to a Claus plant. The resulted A hybrid solvent - membrane systems was also evaluated to see the
hydrogen-rich stream is then set for purification in a Pressure Swing overall influence of the combined system on the heat duty for solvent
Adsorption (PSA) unit (if hydrogen is the final product) or used for regeneration as well as the power duty related to the membrane. The
various energy-related processes (e.g., gas turbine, fuel cells etc.). The best location of the membrane unit was considered to be at the top of
most common utilization of PSA tail gas is for the energy recovery (e.g., chemical scrubbing system (as presented in Fig. 5). In this way the key
power generation in a combined cycle) in order to contribute to the plant advantages of both systems (higher gas separation selectivity and
heat and power ancillary demand. The basic design of green hydrogen captured CO2 purity for the chemical scrubbing and the lower ancillary
generation using the biomass gasification system with CO2 capture energy consumption for the membrane) were used. In addition, it is
feature is exhibit in Fig. 1 [26]. expected that this configuration will decrease the thermal duty of
The CO2 capture from shifted syngas can be achieved in different desorption column. Fig. 5 presents the conceptual layout of pre-
options as presented below. The conventional process applied in various combustion CO2 removal arrangement done by a hybrid chemical sol
applications is using chemical or physical scrubbing. The chemical gas- vent - membrane unit [19].
liquid absorption involves reactions between CO2 and solvent (e.g., The above presented CO2 capture technologies were integrated in a
alkanolamines, ammonia, inorganic hydroxides) Using MDEA as illus biomass gasification plant for green hydrogen production. All CO2
trative chemical solvent, the syngas decarbonization was based on the capture concepts have 90% decarbonization yield. In term of captured
following reversible process [27]: CO2 stream composition, the volumetric purity presented in relevant
literature reference [29] was used (>95% carbon dioxide, <1500 ppm
+
CO2(g) + MDEA(l) + H2 O(l) ↔ MDEAH(l) + HCO−3 (l) (1)
carbon monoxide, <300 ppm water, <50 ppm sulphur compounds and
The presence of a chemical reaction between CO2 and solvent posi <4% other non-condensable gases).
tively increases the selectivity of decarbonization process together with
the purity of captured CO2 flow. As a negative consequence, the solvent 3. Case studies, main design assumptions, thermal integration
regeneration (the reverse reaction to discharge CO2) has an important and model validation
thermal duty. Fig. 2 presents the conceptual layout of CO2 removal in a
pre-combustion capture arrangement in which the solvent regeneration The following case studies of decarbonized green hydrogen pro
is done thermally [12]. duction using biomass gasification were evaluated.
In case of physical solvents, no chemical reactions with CO2 are Case 1. Biomass gasification plant without CO2 capture;
involved. In this case, the situation is reversed compared to chemical
absorption: the overall CO2 removal selectivity decreases but the heat Case 2. Decarbonized biomass gasification plant by chemical scrub
requirements for solvent regeneration decrease also. The regeneration of bing (MDEA);
Case 3. Decarbonized biomass gasification plant by physical scrubbing
(Selexol™);
Case 4. Decarbonized biomass gasification plant by membrane
technology;
Case 5. Decarbonized biomass gasification plant by hybrid solvent -
membrane.
As evaluated gasification reactor, the Shell design (dry feed with
syngas quench) operated at 40 bar was used [27]. The main reasons to
select this gasification reactor are the following: (i) superior energy
conversion yield due to the merge of dry feed configuration (using ni
trogen as pneumatic transport gas) with syngas quench design (capable
to generate high and medium steam from syngas cooling process); (ii)
clean syngas (free from pyrolysis products) due to high operational
temperature (>1400 ◦ C); (iii) high operational pressure (40 bar) which
is relevant for both CO2 capture and hydrogen production features; (iv)
significant industrial experience for processing various fuels (fossil,
biomass, wastes). Oxygen (to be produced by a cryogenic system)
together with steam (generated from available plant hot streams) were
considered as gasification reactants. As fuel, sawdust and residual wood
Fig. 1. Basic design of decarbonized green hydrogen generation using biomass
were considered based on the large availability as well as good
gasification.
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C.-C. Cormos Energy 270 (2023) 126926
hydrogen purification was also used. The most relevant design charac
teristics are shown in Table 1.
The design assumptions mentioned in Table 1 were employed for
assessment of biomass-based gasification systems with CO2 capture for
green hydrogen production. As simulation software, ChemCAD [31] was
used based on its capability to handle modelling and simulation of
process systems present in the evaluated concepts (e.g., biomass char
acterisation, gasification, syngas conditioning train, AGR for desulphu
rization and decarbonization, hydrogen purification, heat recovery and
power generation). As used thermodynamic packages:
Soave-Redlich-Kwong (SRK) model was utilized for the majority of
process sub-systems (e.g., biomass gasification, syngas treatment line,
Fig. 4. Conceptual design of membrane unit for CO2 removal. hydrogen purification) due to the fact that this model is recommended
for appropriate characterisation of gaseous streams at moderate to high
combustion properties (high calorific value, low ash and sulphur con pressure levels; Electrolyte model was used for chemical gas-liquid ab
tents). In addition, various other biomass residues (e.g., agricultural sorption (H2S and CO2 removal) due to the fact that it is recommended
wastes, sewage sludge, meat and bone meal etc.) can be used to provide for characterisation of aqueous solutions with ionic dissociation as
the required fuel input for decarbonized green hydrogen production present in the case of investigated chemical solvents and the TEG
with similar performances [30]. Dehydration model was used for carbon processing unit (CPU) due to the
All evaluated case studies were evaluated in a thermally integrated fact that this model is recommended for the moisture removal from
mode - the available hot sources within the plant were used for steam gaseous streams using tri-ethylene-glycol.
generation which then was used to cover the process requirements In view of optimization of energy efficiency, detailed thermal
(gasification, shift conversion, CO2 capture unit) as well as overall en assessment was done for all investigated concepts in order to find the
ergy ancillary consumptions. In addition, the tail gas resulted from best utilization of hot process streams (called hot sources) within the
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Fig. 5. Conceptual design of hybrid solvent - membrane unit for CO2 removal.
plant e.g., coupling to the cold process streams (called cold sinks) to
avoid utilization of external energy utilities and for steam generation - Hydrogen thermal output of the plant was calculated considering the
[32]. Since there are significant hot sources within the evaluated con hydrogen flowrate and its lower heating value (LHV):
cepts (e.g., raw syngas cooling, shift reactors, Claus plant), the pinch
Hydrogen thermal output = FHydrogen ⋅LHVHydrogen [MW] (3)
method was used as thermal integration tool to optimize overall energy
utilization [33]. Fig. 6 shows the thermal integration analysis in form of
composite curves (hot - HCC and cold - CCC) for gasifier, syngas pro - Net electrical efficiency was assessed considering the net power
cessing train and WGS conversion. output (Wnet ) and the biomass thermal input (QBiomass ):
In view of model validation, the main simulation results were
Wnet
benchmarked against either industrial data collected from relevant Net electrical efficiency = • 100 [%] (4)
FBiomass ⋅ LHVBiomass
literature sources [22,25], IGCC and AGR process licensors [23] or
IEAGHG reports [27] or against experimental data [34,35]. For each
relevant plant sub-system (e.g., gasification island, syngas treatment - Cumulative energy efficiency was determined taking into consider
line, water gas shift conversion, AGR using various technologies, ation the hydrogen and electricity combined production and the
hydrogen purification unit etc.), the main performance indicators were biomass thermal input (QBiomass ):
analysed. For example, in case of biomass gasification unit, the fuel
FHydrogen ⋅ LHVHydrogen + Wnet
conversion yield, overall energy conversion efficiency defined as cold Cumulative efficiency = • 100 [%] (5)
FBiomass ⋅ LHVBiomass
gas efficiency, syngas characteristics (e.g. composition, pressure) were
assessed. For instance, in term of biomass conversion, the simulation
results give an average 99% yield in comparison to experimental values - CO2 capture rate was computed taking into consideration captured
of more than 98.5% [15]. The same can be observed for the WGS con CO2 molar flow (FCaptured CO2 ) and the molar from of carbon content in
version (98% vs. 97–99% [10]), CO2 capture rate (90% for both simu the biomass (FBiomass carbon ):
lation and experimental data as considered in mostly CCS projects [36, FCaptured CO2
37]), hydrogen purification yield (85% vs. 82–87% [27]) etc. As can be CO2 capture rate = • 100 [%] (6)
FBiomass carbon
noticed, no relevant differences were noted among the key results from
simulation and real plant (experimental) data.
- Plant specific CO2 emission was calculated taking into account the
4. Techno-economic assessment methodology and used mass flow of emitted CO2 (FEmitted CO2 ) reported to the combined
economic assumptions production of hydrogen and power:
[ ]
FEmitted CO2 kg
After modelling, simulation, model validation and thermal integra Specific CO2 emissions = (7)
FHydrogen ⋅ LHVHydrogen + Wnet MWh
tion of the investigated concepts, the main techno-economic perfor
mance indexes were assessed using overall mass and energy balances.
The used performance indexes are fully in line to the current agreed - Specific solvent regeneration duty was assessed as the reboiler heat
methodology within the field (e.g., reports from International Energy duty of the desorption column reported to the mass flow of captured
Agency Greenhouse Gas R&D Programme (IEAGHG) [36], National CO2:
Energy Technology Laboratory (NETL) [37] etc.). As for technical per [ ]
QDesorption column MJ
formance indexes, the next parameters were used. Solvent regeneration duty = (8)
Captured CO2 flowrate kg
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Table 1
Key design characteristics of process sub-systems.
Biomass (sawdust) characteristics Mass composition (dried-based): 49.20%
carbon, 5.99% hydrogen, 0.82% nitrogen,
42.98% oxygen,
0.03% sulphur, 0.98% ash; Water content:
10%;
Inferior calorific value: 18.11 MJ/kg
Oxygen supply (cryogenic-based air Oxygen flow composition (vol. %): 95%
separation unit) [26] oxygen, 2% nitrogen, 3% argon
ASU electrical utilization: 200 kWh/ton O2
ASU oxygen delivery pressure: 2.4 bar
Biomass handling and transport [26] Milling energy consumption: 1% of thermal
input
Biomass transport to gasifier: 0.12 kg N2/kg
Gasifier unit [25] Shell gasifier
Oxygen to biomass mass ratio: 0.85
Steam to biomass mass ratio: 0.14
Gasifier operating parameters: 1425 ◦ C & 40
bar Fig. 6. Composite curves for gasifier, syngas processing line and
Gas cooling outlet temperature: 875 ◦ C WGS conversion.
Syngas water gas shift (WGS) Sulphur tolerant catalyst
conversion stage [27] 2 shift reactors operated in adiabatic mode
Steam to carbon monoxide molar ratio: 2
In respect to the economic indicators of the evaluated biomass-based
Conversion rate: >97% green hydrogen production concepts with decarbonization feature, the
Pressure reduction: 1.25 bar/catalytic bed following parameters were used.
Acid Gas Removal (AGR) unit - 50% wt. MDEA aqueous solution - Investment cost (CAPEX) of the evaluated green hydrogen pro
Chemical gas-liquid absorption H2S removal rate: 98%
duction concepts was calculated considering the main plant components
[27] CO2 removal rate: 90%
Regeneration of solvent: thermal (LP steam) (e.g., biomass processing, oxygen supply unit, gasification island, syngas
Acid Gas Removal (AGR) unit Selexol™ process treatment line, acid gas removal, hydrogen purification, carbon pro
-Physical gas-liquid absorption H2S removal rate: 98% cessing etc.). In these plant sub-systems, the capital cost (CE) for a
[23] CO2 removal rate: 90%
certain production capacity (Q) was assessed using the reference cost
Regeneration of solvent: pressure reduction
Acid Gas Removal (AGR) unit H2-selective membrane
data (reference investment costs - CB, reference sizes - QB and an
-Membrane [28] CO2 removal rate: 90% exponent - M) as shown in equation (10). Used reference data for CAPEX
Membrane permeance data: H2 - 300, CO2 - calculation (updated to the year 2022 using the Chemical Engineering
10, CO - 4, N2 - 2, Ar - 2, CH4 - 2, H2O - Plant Cost Index - CEPCI [39]) are presented in Table 2:
10,000
Pressure ratio: 5 - 10
( )M
Q
Carbon processing unit (CPU) for Moisture removal: Tri-ethylene-glycol (TEG) Capital cost (CE ) = CB • [€] (10)
CO2 conditioning [26] Delivery pressure: 120 bar
QB
Compressing unit efficiency: 85%
Composition (vol.): min. 95% carbon
dioxide, max. 2000 ppm carbon monoxide, - Specific CAPEX was computed as the investment cost (CAPEX) re
max. 250 ppm water, max. 40 ppm sulphur ported to the combined production of hydrogen and power:
compounds, max. 4% other non-condensable [ € ]
gases (e.g., hydrogen, nitrogen etc.) Total investment cost
Specific CAPEX = (11)
Claus unit for sulphur removal [27] Oxygen-blown unit FHydrogen ⋅ LHVHydrogen + Wnet kW
Sulphur (H2S) content at plant inlet: min.
25% (vol.) -Operational & maintenance (O&M) costs are estimated considering
Hydrogen purification unit [27] Purity & pressure: min. 99.95% vol. & 60 bar both components: fixed and variable costs. The fixed cost covers main
Compressing unit efficiency: 80% tenance, direct labour cost, administrative, support and overhead costs.
PSA tail gas integrated for energy recovery
Variable cost covers materials directly linked to production process (e.
Heat recovery and power block [26] Steam conditions: 560 ◦ C & 120 bar/200 ◦ C
& 3 bar g., biomass, catalysts, solvent, membrane, waste disposal, make-up
Efficiency of steam turbine: 85% water etc.). Key economic assumptions employed for O&M calculation
Steam final expansion: 0.045 bar are shown in Table 3.
Minimum temperature difference: ΔTmin. =
10 ◦ C
- Levelized cost of hydrogen (LCOH) is assessed as ratio of annualized
CAPEX and O&M costs to the combined hydrogen and power pro
duction as follow:
efficiencies and the plant CO2 emissions for the decarbonized and Annualized CAPEX + Operational & maintenence cost [ € ]
non-decarbonized concepts [38]: LCOH =
FHydrogen ⋅ LHVHydrogen + Wnet MWh
(12)
( )
3600 ⋅ 1
− 1 [ ]
MJ
(9)
Cumulative efficiencyCO2 capture Cumulative efficiencyNo capture
SPECCA =
Specific CO2 emissionsNo capture − Specific CO2 emissionsCO2 Capture kg
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Table 2
Economic reference data for CAPEX calculation.
Plant component Process parameter to scale Reference cost (M€) Reference size Exponent Reference
Biomass handling unit Biomass flow t/h 57.50 200.00 0.75 [26]
Cryogenic oxygen supply unit Oxygen flow t/h 168.18 225.00 0.75 [27]
Gasifier island Biomass flow t/h 307.80 270.00 0.80 [26]
Syngas treatment unit Biomass flow t/h 73.92 280.00 0.80 [26]
Decarbonization unit (MDEA) Captured CO2 flow t/h 10.78 14.00 0.60 [27]
Decarbonization unit (Selexol™) Captured CO2 flow t/h 122.00 550.00 0.70 [27]
Decarbonization unit (membrane) Membrane surface 106 m2 42.00 1.00 1.00 [19]
Syngas desulfurization Sulphur flow t/h 40.92 2.40 0.75 [27]
CO2 processing unit (CPU) Captured CO2 flow t/h 36.30 550.00 0.80 [26]
Hydrogen purification Hydrogen flow t/h 19.80 20.00 0.75 [27]
Heat recovery and power block Gross power output 264.00 500.00 0.75 [27]
Table 3 Table 4
Economic assumptions used for O&M cost estimation. Main technical and environmental performance indexes.
Biomass price 4.00 €/GJ (72.40 [40] Parameter U.M. Case 1 Case 2 Case 3 Case 4 Case 5
€/t)
Biomass input t/h 117.50
MDEA price 4800.00 €/t [26] Biomass calorific MJ/ 18.11
Selexol™ price 6400.00 €/t [26] value kg
Boiler water price 0.15 €/t [21] Biomass thermal MWth 591.10
Cooling water price 0.01 €/t [21] input (A)
Cooling water treatment cost 0.003 €/m3 [21] PSA tail gas energy MWe 31.40 29.52 29.70 29.95 29.75
Boiler water treatment cost 95,000 €/month [21] recovery
Sulphur price 120.00 €/t [21] Steam turbine MWe 51.75 49.30 51.60 51.14 50.00
Cost for ash disposal 16.00 €/t [21] power output
Number of direct personnel 96 persons [26] Gross power output MWe 83.15 78.82 81.30 81.09 79.75
Average annual direct personnel cost 48.00 k€/person/y [26] (B)
Administrative costs 35% of labour cost [27] Ancillary MWe 25.20 41.25 38.95 36.10 39.21
Maintenance costs (percentage of annual capital 4.00% [27] consumption (C)
cost) Hydrogen output MWth 300.00 300.00 300.00 300.00 300.00
Working capital 30 days’ supply [27] (D)
Plant operational factor 90% [27] Net power output MWe 57.95 37.57 42.35 44.99 40.54
Interest rate 8.00% [27] (E = B - C)
Captured CO2 transport and storage cost 15.00 €/t [26] H2 efficiency (D/ % 50.75 50.75 50.75 50.75 50.75
CO2 emission tax 0.00 €/t [41] A*100)
Plant erection time 3 years [27] Power efficiency % 9.80 6.35 7.16 7.61 6.85
Productive operational time 25 years [27] (E/A*100)
Cumulative energy % 60.55 57.10 57.91 58.36 57.60
efficiency
- CO2 removal and avoided costs were computed using levelized cost Decarbonization % 0.00 90.00 90.00 90.00 90.00
of hydrogen (LCOH), captured CO2 mass flow and specific CO2 rate
CO2 specific kg/ 530.10 60.05 59.21 58.77 59.52
emissions for both capture and non-capture concepts: emissions MWh
[€] Regeneration duty MJ/ – 0.58 – – 0.46
LCOHCapture − LCOHNo capture
CO2 removal cost = (13) (solvent) kg
Captured CO2 mass flow t Membrane power kWh/ – – – 47.36 20.25
consumption t
[€]
LCOHCO2 capture − LCOHNo capture SPECCA MJ/ – 0.76 0.57 0.47 0.64
CO2 avoided cost =
CO2 emissionNo capture − CO2 emissionCO2 capture t kg
(14)
Key economic assumptions employed in the evaluations of green the green hydrogen production based on biomass gasification implies an
hydrogen production based on biomass gasification are presented in energy penalty in form of a reduction of the cumulative energy effi
Table 3. ciency compared to the benchmark non-capture case. The decarbon
ization energy penalty is approximate 2.2–3.45 net percentage points.
5. Results and discussions of green hydrogen production from The smallest CO2 capture energy penalty is reported for the membrane
biomass gasification technology (Case 4) and the highest one for the chemical scrubbing
technology (Case 2). Physical scrubbing (Case 3) and hybrid absorption -
5.1. Technical and environmental performance indexes membrane (Case 5) decarbonization technologies show close energy
penalties with a plus for the physical absorption. All decarbonized
Overall mass & energy balances were utilized to quantify the most hydrogen production systems have a CO2 capture rate of 90%; the spe
relevant plant performance indexes (as defined in section 4). Table 4 cific CO2 emissions are in the range of 58–60 kg/MWh reporting a sig
shows the most significant technical indexes calculated for the assessed nificant reduction in comparison to the benchmark case (530 kg/MWh).
green hydrogen generation concepts via biomass gasification (both In addition, it worth mention that the decarbonized concepts have
decarbonized and non-capture cases). All concepts have the same negative CO2 emissions considering that the primary fuel (biomass) is of
biomass input (117.50 t/h equivalent to 591.10 MW thermal input) as renewable source. In these conditions, the benchmark concept without
well as the same hydrogen output (100,000 Nm3/h corresponding to CO2 capture (Case 1) can be considered to have zero fossil CO2 emission
300 MW thermal output). and the decarbonized concepts have negative CO2 emissions of about -
As shown in Table 4, the integration of decarbonization step within 470 kg/MWh. This is extremely relevant for the global efforts to reduce
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For utilities and offsite units, the investment cost was assessed as 25%
form process investment [45]. The other costs (owner’s cost, contin hydrogen production based on biomass gasification by about 8–18%.
gencies, permitting, surveying etc.) were estimated as a 25% ratio from The lowest O&M costs are reported for membrane-only concept (Case 4).
total installed costs [46]. The specific CAPEX costs were calculated with The chemical scrubbing (either alone or the hybrid system with mem
formula 11 and they are reported in Fig. 7 for all investigated cases. brane) shows the highest O&M costs mainly due to superior solvent
As shown, the decarbonization of green hydrogen production based costs. The physical scrubbing has lower O&M costs in contrast to
on biomass gasification induces a relevant increase of CAPEX costs chemical gas-liquid absorption system but higher than the membrane
compared to the benchmark case. The membrane decarbonization concept.
technology has the lowest CAPEX (about 1888 Euro/kW of hydrogen
and power) followed by the chemical and physical scrubbing which
show small differences between them (2035–2040 Euro/kW). The
hybrid absorption - membrane concept has the highest CAPEX (about
2130 Euro/kW). This can be explained by the fact that the bulk of CO2
removal is done by chemical scrubbing and additionally a membrane
unit was used.
The followed relevant economic performance index was the Opera
tional & Maintenance (O&M) costs (OPEX). The main economic as
sumptions used for O&M cost assessment were reported in Table 3. The
O&M costs for green hydrogen production systems with and without
CO2 capture feature are shown in Fig. 8.
Fig. 9. Sensitivity evaluation for levelized cost of hydrogen (Case 4).
The O&M costs are increasing with decarbonization of green
Fig. 7. Specific CAPEX costs for assessed green hydrogen production concepts.
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C.-C. Cormos Energy 270 (2023) 126926
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C.-C. Cormos Energy 270 (2023) 126926
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