Photocatalytic reactors use artificial ultraviolet light to oxidize methane. Air must be moved through the localized reactor, either through active methods such as fans, or passive methods such as solar updraft chimneys that use convective heat transfer to move air.
Photocatalytic reactors are promising for breaking down methane at its emission sources where its concentration is elevated. For photocatalytic reactors to be a feasible atmospheric methane removal approach there would have to be a >200x improvement in catalytic efficiency and extremely low energy airflow. The required airflow to achieve megaton scale atmospheric methane removal would be far beyond planned carbon dioxide direct air capture capacity in the upcoming few decades.
Significant improvements in catalytic efficiency would be necessary to make photocatalytic reactors viable to operate atmospheric methane concentrations. For this application, they are currently climate detrimental and cost-implausible.
A key metric for determining cost and climate impacts for photocatalysis is Apparent Quantum Yield (AQY), the ratio of incident photons to oxidized methane molecules. This determines the energy input required to produce artificial light to oxidize methane. Cost and climate impacts are also driven by the energy requirements to move air through the reactor. This could be negligible for passive air flow, but significant for active air flow methods. Where artificial light is required, the energy requirements to generate it add to the cost. Sunlight does not provide a high enough photon flux to be a viable alternative.
Assuming best-case 2030 energy cost and carbon footprint projections are met, current photocatalytic reactors are not climate beneficial or cost-effective. Before taking into account airflow requirements, the minimum AQY thresholds are ~0.1% for climate beneficial, ~1.4% for cost-plausible, and ~7% for cost-effective. The best AQY measured so far is ~0.03% for 2 ppm methane, so at least a 200x increase in AQY is required to be climate beneficial and cost-effective.
The potential scale photocatalytic reactors could reach is limited by the energy requirements of air movement and potentially resource limitations of raw materials. Given the low atmospheric concentration of methane, any flow through system would have to process massive amounts of air to oxidize a benchmark annual scale of 10 million metric tons of methane (830 Mt CO2e using GWP20). For example, if you add methane breakdown reactors to every carbon dioxide direct air capture system that is projected to be installed by 2030 (~60 Mt CO₂/yr or around 5 billion cubic feet per minute), only around 0.1 Mt/yr of methane could be removed.
Even if photocatalytic reactors become feasible, the amount of methane addressed will be directly related to the number and scale of the reactors built, and resource intensive to reach meaningful scale. Therefore we estimate an approach of this sort would take decades to scale after feasibility was established.
In a closed reactor system, byproducts could be measured in situ and potentially be selectively removed, reducing the uncertainty as to what gasses would be produced and emitted. This drastically lowers the health and environmental risks compared to open system interventions.
In addition to methane, photocatalysts are expected to react with other atmospheric pollutants, including sulfur dioxide (SO₂), carbon monoxide (CO), ozone (O3) and non-methane volatile organic compounds (NMVOC). These compounds also contribute to climate change and the positive and negative climate impacts of their breakdown would need to be accounted for. Increasing oxidation of these species could have additional air quality benefits near ground level. However, photocatalysts are also known to generate undesirable end products (nanoparticles, secondary volatile organic compounds, etc.). More research is needed to better understand the tradeoffs between these potential positive vs. negative impacts.
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