This appendix describes research, development, and demonstration (RD&D) needs for the crosscutting technologies of CO2 capture and CO2 purification. Additional crosscutting research needs for markets, life cycle assessment and techno-economic assessment, policy, and infrastructure are covered in Chapters 2, 3, 4, and 10, respectively.
Common to all CO2 utilization processes is the need first to capture CO2 from a point source, the air, or the ocean.1 As discussed in the committee’s first report, there are a variety of carbon capture technologies at different technology readiness levels (TRLs) (see NASEM 2023, Table 4.1), and the choice of capture technology will depend on “the initial and final desired CO2 concentration (i.e., the percentage of CO2 to be removed), scale of CO2 capture, operating pressure and temperature, composition and flow rate of the gas stream, integration with the original facility, and cost considerations” (NASEM 2023, p. 75). The cost and energy requirements for CO2 pressurization are important considerations for the viability of a CO2 utilization project, and capture systems that release CO2 at the pressures required for transportation or downstream processing (i.e., conversion) are preferred to reduce or eliminate compression costs. Table F-1 shows the approximate concentration of CO2 from different sources, the total annual U.S. emissions from each source type (where applicable), and estimated capture costs.
Government-supported demonstration of CO2 capture projects, integrated with transport and storage technologies, can further the deployment and replication of CO2 capture technologies. These demonstrations enable modularization of equipment at scale that may reduce construction costs, increase capture efficiency as improved technologies become available to substitute for current ones, and provide operational data that can build confidence with project investors and reduce financing risks. Beyond cost reductions achieved through learnings from technology scale up, additional RD&D on capture technologies will also be important for decreasing CO2 capture costs. Table 4.2 from the committee’s first report (NASEM 2023), which is reproduced and expanded upon in Table F-2 below, outlines RD&D targets to reduce costs from different classes of capture technologies. RD&D needs for enabling technologies, which could benefit multiple capture systems, include mitigating aerosol emis-
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1 In some systems, capture and conversion of CO2 are integrated, as described in Chapter 7, Section 7.2.5.
TABLE F-1 CO2 Concentration, Annual U.S. Emissions, and Estimated Capture Costs from Different Sources
| Source | CO2 Concentration (percent by volume) | Annual U.S. Emissions | Estimated Capture Cost ($/t CO2) |
|---|---|---|---|
| Power Generation | Natural gas-fired: 3–6a,b Coal-fired: 11–15a,b |
1500 MMTc | 40–290c,d |
| 73–167d,e (coal) | |||
| 82–166d,e (natural gas) | |||
| 100–123d,f,g (coal) | |||
| 82–98d,f,h (coal) | |||
| 104–133d,f,g (natural gas) | |||
| 84–105d,f,h (natural gas) | |||
| 83–268i,j (coal) | |||
| 93–290i,j (natural gas) | |||
| 53–86i,k (coal) | |||
| Cement | Process emissions: ~14–33c | 66 MMTc | 45–120c,d |
| 87–131d,e | |||
| 89–109d,f,g | |||
| 76–90d,f,h | |||
| 64–95i,j | |||
| 61–94i,k | |||
| 61–64i,l | |||
| Iron and Steel | ~17–27c,l,m | 62 MMTc | 40–130c,d |
| 54–69d,e | |||
| 108–121d,f,g | |||
| 90–109d,f,h | |||
| 75–113i,j | |||
| 75–119i,k | |||
| 65–67i,l | |||
| Hydrogen Production | 14–45b | 100 MMTn | 103–129d,f,g (SMR 90 percent capture) |
| 83–102d,f,h (SMR 90 percent capture) | |||
| 61–88i,j | |||
| 68–114i,k (SMR and steam production, 90 percent capture) | |||
| Ethanol Production | ≥95b,c | 45 MMTc | 0–35c,d |
| 42–59d,e | |||
| 36–41d,f,g | |||
| 33–37d,f,h | |||
| 24–34i,j | |||
| 18–26i,k | |||
| 32i,l | |||
| Natural Gas Processing | CO2 vent: 99b | 26.1 MMTo | 32–35d,f,g |
| 29–32d,f,h | |||
| 23–35i,j | |||
| 14–20i,k | |||
| 16i,l | |||
| Direct Ocean Capture | ~6, varies with pH and temperature | N/A | 150–2500d,p |
| Source | CO2 Concentration (percent by volume) | Annual U.S. Emissions | Estimated Capture Cost ($/t CO2) |
|---|---|---|---|
| Direct Air Capture | 0.04b | N/A | 600–1000i,q |
| 225–600i,k | |||
| 89–877i,r,s (sorbent-based) | |||
| 156–506i,r,s (solvent-based) |
d Measured in $/ton of CO2.
g Estimated for first-of-a-kind facility.
h Estimated for nth-of-a-kind facility.
i Measured in $/tonne of CO2.
j Table 2-7 of NPC (2019).
m Emission streams in this range are blast furnace stove, power plant stack, and coke oven gas.
o Table 3-73 of EPA (2023).
p Capture costs for electrochemical processes; NASEM (2022).
s Cost of net CO2 removed, accounting for any CO2 emissions from powering the direct air capture system.
TABLE F-2 Research, Development, and Demonstration Targets to Improve Carbon Capture Systems
| CO2 Capture Technology | Research Trends for Reducing Carbon Capture Costs |
|---|---|
| Solvents |
|
| Sorbents |
|
| Membranes |
|
| Novel concepts |
|
SOURCES: NASEM (2023, Table 4-2); NETL (2020, n.d.(b)).
sions; improving stability, compatibility, and corrosion resistance; and reducing viscosity and degradation products (Bostick et al. 2021; NETL n.d.(b)). Basic science and applied research needs to advance solvent- and sorbent-based direct air capture (DAC) technologies, including synthesizing and testing new materials; designing and testing new equipment and system concepts; performing independent materials testing, characterization, and validation; and establishing and managing a public materials database (NASEM 2019b). For electrochemical direct ocean capture (DOC) technologies, research needs include new designs for electrochemical reactors; novel electrode and membrane materials; systems integration with rock dissolution; and demonstration projects to verify carbon removal, monitor environmental impacts, and investigate scale-up strategies (NASEM 2022).
Direct conversion of impure CO2 streams to products can reduce the net energetic and capital costs of CO2 utilization, as an intermediary purification step is not required. This process, termed “integrated CO2 capture and conversion” in this report, is described in detail in Chapter 7. Primary research needs for integrated capture and conversion include discovery of relevant molecules and materials, understanding of catalytic mechanisms, process optimization, and reactor design.
Most CO2 transport, utilization, and storage applications require the removal of at least some impurities present in the CO2 gas streams. The committee’s first report (NASEM 2023) contained a robust discussion of typical impurities present in CO2 gas streams (Tables 4.3 and 4.4), impurity thresholds for different CO2 transport modes (Table 4.5), and impurities of concern for CO2 utilization routes (Table 4.6). Appendix H of this report reproduces Tables 4.3 and 4.4 (as Tables H-1 and H-2, respectively) and updates Table 4.5 (as Table H-3) based on more recent information. Table 4.6 is reproduced as Table 3-1 in Chapter 3. From this assessment, the committee concluded that the impurities present in CO2 streams may influence the viability of utilization processes, with mineralization and biological conversion being the most resilient to impurities2 and electro- and thermochemical conversions being the most sensitive (Finding 4.3, NASEM 2023). The lack of standard specifications for CO2 purity across capture, transport, utilization, and storage could result in increased energy and operational costs for some stakeholders, as well as efficiency losses throughout the value chain (Neerup et al. 2022). Common separation technologies used to reach very pure streams (akin to food-grade CO2) are capital- and energy-intensive. Examples are cryogenic distillation and pressure-swing adsorption. These types of purification technologies, therefore, can become a key bottleneck to achieve cost-effective CO2 utilization, let alone to run such CO2 utilization processes flexibly. Ongoing research is investigating CO2 conversion catalysts and technologies that can tolerate impurities (see, e.g., Harmon and Wang 2022; Ho et al. 2019), which might improve the economic feasibility of some CO2 utilization systems. As discussed in Chapter 7, more research is needed to develop CO2 conversion catalysts that are impervious to impurities. Additionally, developing standards and methodologies for measuring ppm or ppb levels of impurities in CO2 streams will help to inform RD&D on CO2 capture and utilization technologies.
The specific separation technology to be used must be selected with the contaminants and desired CO2 purity in mind. For example, membranes today would be exceptionally effective at dehydrating CO2 streams and could remove contaminants such as hydrogen sulfide (H2S), but they still require significant development to increase their cost-effectiveness and performance in harsh feed conditions. Furthermore, there is a need to develop performance-tuned membrane materials that can handle gas flow rates and compositions that change with time. This will especially be important for CO2 utilization technologies that target CO2 from (bio)waste feedstocks. Membranes tuned to separate H2S would not remove contaminants such as N2, O2, or argon. Monoethanolamine-based approaches necessarily leave the purified CO2 stream saturated with water. Sorbents could be rapidly saturated with even low levels of condensable components. Developing more efficient CO2 separation methods and hybrid separation technologies, rather than relying on a single method or approach, will likely yield the most promising separation results.
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2 Notably, however, anaerobic biological conversion is sensitive to oxygen, and purification to remove oxygen can be energy-intensive.
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