Solar-Powered Direct Air Capture: Techno-Economic and Environmental Assessment Notes

Overview of Direct Air Capture (DAC) and Study Objectives

  • Direct Air Capture (DAC) Definition: Technologies that separate and concentrate atmospheric carbon dioxide solely through mechanical and chemical processes, excluding biogenic sources. Unlike biomass-based processes, DAC does not present biophysical limitations that threaten crop production or biodiversity when scaled up.

  • Goal of DAC: The captured CO2CO_2 can be sequestered (Direct Air Carbon Capture and Storage, or DACCS) or used as a feedstock for carbon-neutral chemicals and fuels. These synthetic fuels are critical for decarbonizing hard-to-abate sectors.

  • Primary Technologies:

    • Solid Sorbent DAC (S-DAC): Captures CO2CO_2 using solid sorbents, regenerated with vacuum and low-temperature heat (100C\approx 100\,^\circ\text{C}). While it can use waste heat, it consumed more energy than L-DAC in some assessments and requires durable, efficient sorbents.

    • Liquid Solvent DAC (L-DAC): Employs a liquid alkali solution to form carbonates, which are calcined at high temperatures (900C900\,^\circ\text{C}) to release pure CO2CO_2.

  • The Problem with Conventional L-DAC: Advanced concepts use oxyfuel combustion of natural gas for calcination. This creates a stream containing roughly one-third fossil CO2CO_2, hindering its use for fully carbon-neutral products.

  • Proposed Solution: This study assesses a solar-powered L-DAC approach using Solar Thermal Energy (STE) to provide green high-temperature heat (> 1000\,^\circ\text{C}), particularly in arid regions with high solar resources.

Technical Process of Solar Liquid Direct Air Capture (L-DAC)

  • Carbon Engineering Ltd. Baseline: The study modifies the process originally published by Carbon Engineering Ltd., which captures CO2CO_2 in two main cycles.

  • Cycle 1: Alkali-Carbonate Cycle

    • Air Contactor: Atmospheric air is propelled by fans through packing material moistened by an alkali solution (potassium hydroxide, KOHKOH). The CO2CO_2 reacts to yield potassium carbonate (K2CO3K_2CO_3).

    • Pellet Reactor: K2CO3K_2CO_3 reacts with calcium hydroxide (Ca(OH)2Ca(OH)_2) to form calcium carbonate (CaCO3CaCO_3) and regenerates the KOHKOH, which is recirculated back to the contactor.

  • Cycle 2: Calcination-Slaking Cycle

    • Solar Calciner: Substitutes the gas-fired calciner. CaCO3CaCO_3 is calcined using solar thermal energy at 900C900\,^\circ\text{C} to produce pure CO2CO_2 and calcium oxide (CaOCaO).

    • Steam Slaker: CaOCaO is combined with water in a highly exothermic reaction to produce Ca(OH)2Ca(OH)_2, completing the loop.

  • System Modifications for Solar Power:

    • Elimination of the air separation unit, gas turbine, and flue gas CO2CO_2 absorber.

    • Division into a Continuous Section (air contactor, slaker, pellet reactor) and an Intermittent Section (solar calcination).

    • Energy Recovery: Two steam turbines extract electricity from waste heat—one continuous (from the slaker) and one intermittent (from the CO2CO_2 gas cooler and heat recovery steam generator, HRSG).

    • Buffering and Storage: Inclusion of solid storage units (for CaOCaO and CaCO3CaCO_3), water/CO2CO_2 tanks, and an auxiliary Photovoltaic (PV) plant with batteries to ensure autonomous, stable operation and 100% green power matching.

Modeling and Methodology

  • Simulation Software: Aspen Plus V12.1 was used for steady-state simulation; DLR’s HFLCAL VH13 was used for solar field layouts.

  • Solar Calcination Parameters:

    • Technology chosen: CentRec centrifugal particle receiver (high Technology Readiness Level, TRL).

    • Design heat output: 41.7MWth41.7\,MW_{th} per tower.

    • Reactor efficiency: 87.8%87.8\% at 900C900\,^\circ\text{C}.

    • Heat requirement: 1.51MWh/tCO21.51\,MWh/t\,CO_2.

    • Daily start-up cost: 10%10\% of average daily heat collected is discarded for cold start-up.

  • Air Contactor Parameters:

    • Air velocity: 1.4m/s1.4\,m/s.

    • Pressure drop: 100Pa100\,Pa.

    • Fan efficiency: 70%70\%.

    • Atmospheric CO2CO_2: 420ppm420\,ppm.

  • Geospatial Screening Criteria (282 polygons identified):

    • Coastal limit: Less than 100km100\,km from the ocean (to facilitate desalination).

    • Latitude: Below 4545\,^\circ in both hemispheres.

    • Slope: Maximum slope less than 2.1%2.1\%.

    • Land Cover: Limited to shrubs, herbaceous, or bare/sparse vegetation; excluded protected areas.

Economic Assessment Framework

  • CAPEX Calculation:

    • CAPEX=Field+Non-field+ContingencyCAPEX = \text{Field} + \text{Non-field} + \text{Contingency}

    • Field Cost=1.127×Lang Factor×Equipment Cost Correlation\text{Field Cost} = 1.127 \times \text{Lang Factor} \times \text{Equipment Cost Correlation}

    • Non-field=0.233×Field\text{Non-field} = 0.233 \times \text{Field}

    • Contingency=0.2×Field\text{Contingency} = 0.2 \times \text{Field}

    • Lang Factor applied: 44.

  • Levelized Costs:

    • Levelized Cost of Produced CO2 (LCOP): Total annual costs divided by CO2CO_2 production.

    • Levelized Cost of Removed CO2 (LCOD): Subtracts indirect greenhouse gas (GHG) emissions and fossil CO2CO_2 from the production total. It includes an onshore sequestration cost of 10USD2022/tCO210\,USD_{2022}/t\,CO_2.

  • Natural Gas Scenarios for Comparison:

    • US Scenario: 7.617USD2022/GJLHV7.617\,USD_{2022}/GJ_{LHV}.

    • EU Scenario: 23.590USD2022/GJLHV23.590\,USD_{2022}/GJ_{LHV}.

  • WACC (Weighted Average Cost of Capital): Found to be a major cost driver, varying by country (e.g., higher in developing economies).

Environmental Performance and Site Selection Results

  • Role of Environmental Conditions:

    • Electricity Consumption: Generally higher on western coasts (North/South America, Middle East) due to dry conditions reducing CO2CO_2 removal efficiency, requiring more air to be processed. Low atmospheric pressure at high altitudes also reduces capture per volume of air.

    • Water Losses: High in Red Sea and Persian Gulf regions due to high temperatures and low relative humidity. Conversely, one-third of screened areas show lower water loss (< 4.7\,t\,H_2O/t\,CO_2) than conventional L-DAC estimates.

    • Solar Resource: 60%60\% of analyzed land requires a solar field smaller than 0.3km20.3\,km^2 for a 0.1MtCO2/year0.1\,Mt\,CO_2/year plant.

  • LCOP Global Distribution:

    • With local WACC: Most promising sites are in Southern Europe, Australia, and California (developed economies with low cost of capital).

    • With constant 4.2% WACC: Clusters appear in Peru, Chile, Southern Africa, and the Middle East, reflecting purely technical solar/climatic potential.

  • Cost Breakdown: Solarized L-DAC has a higher CAPEX share (6070%\approx 60-70\%) than conventional L-DAC. Natural gas can account for over 40%40\% of the LCOP in conventional gas-fired systems.

Impact of Scale and Net Carbon Removal (LCA)

  • Economy of Scale: LCOP decreases significantly as capacity increases from 0.050.05 to 0.2MtCO2/year0.2\,Mt\,CO_2/year. Solarized plants show a "sawtooth" cost pattern as new towers must be added discretely (41.7MWth41.7\,MW_{th} limits).

  • Life Cycle Assessment (LCA) Results:

    • Conventional L-DAC generates significant indirect emissions from natural gas extraction and transportation.

    • Solar L-DAC emissions primarily come from construction materials for solar infrastructure.

    • Net emissions for solar power are more than 1 order of magnitude lower than conventional systems.

  • LCOP vs. LCOD Shift:

    • While conventional L-DAC has a lower LCOP (cost per ton produced), solar-powered L-DAC becomes highly competitive or even superior when looking at LCOD (cost per ton effectively removed).

    • Accounting for fossil CO2CO_2 generated by natural gas combustion and indirect GHG emissions causes the cost of conventional DAC to escalate dramatically, making solar-powered L-DAC the most cost-effective and environmentally sound alternative for large-scale CDR.