Experimental study demonstrates continuous indoor carbon dioxide capture using Leptolyngbya photobioreactors, indicating scalable potential for decentralized indoor air remediation.
Elevated indoor carbon dioxide (CO2) represents an underutilized biogenic carbon feedstock. Coupling indoor atmospheric remediation with biological sequestration requires overcoming mass-transfer limitations and culture collapse under high carbon loads. This study empirically evaluated a direct-injection, 2.0 L filamentous Leptolyngbya sp. photobioreactor for continuous indoor CO2 valorization. A fortified nitrogen medium (4.5 g L−1 NaNO3) was utilized to sustain high-density proliferation. Initial optimization confirmed that narrow-band Red LEDs (10,000 lux) maximized the Apparent Quantum Efficiency (ΦCO2) at 1.49 × 10−3 mol/mol. During a 20-day continuous trial under 5000 ppm CO2 sparging, the EPS-rich cyanobacterial matrix resisted acidification, achieving a stationary biomass density of 3.30 g L−1. The system maintained a steady bio-mitigation velocity of ~2120 ppm day−1. Intracellular chlorophyll a peaked at 26.0 mg L−1 on Day 10, before severe optical self-shading induced a 47% photoprotective degradation, defining Day 10 as the optimal biorefinery harvesting threshold. At this peak, dynamic efficiency reached 2.07 × 10−3 mol/mol. Projecting these kinetics onto a 50 m3 occupied room confirms that capturing ambient CO2 requires a working volume of 85–90 L and a spatial footprint of <0.25 m2, validating Leptolyngbya sp. as a highly resilient catalyst for decentralized, commercial-scale indoor bioprocessing.
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Dodangodage et al. (2026) studied this question.
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