Demonstrates enhanced CO2 removal in xenon-rich streams, suggesting improved anesthetic efficiency.
Xenon is a superior anesthetic, yet its clinical use is crippled by the high cost of unrecovered gas, a challenge rooted in the inability to selectively remove CO 2 from humid, Xe-rich exhaled streams. Here, we uncover a strategy that turns water from a performance-degrading agent into a synergistic enhancer. By engineering a sub-10 nm gradient-aminated surface on hollow fiber membranes via controlled NH 3 plasma treatment, we create a confined environment where water molecules play a dual role. They promote the reversible CO 2 -amine reaction to form mobile bicarbonate species, accelerating CO 2 transport, while simultaneously generating steric and competitive adsorption barriers that selectively suppress Xe diffusion. This moisture-synergized facilitated transport mechanism enables the optimized membrane to achieve an unprecedented mixed-gas CO 2 /Xe selectivity of 1105 ± 13 with a CO 2 permeance of 35.3 ± 1.2 GPU under simulated exhaled anesthetic conditions, surpassing all previously reported membranes. The membrane maintains stable operation over 720 h in oxygen-containing feeds, and a home-built module achieves over 99% single-stage CO 2 removal, confirming practical viability. Beyond xenon recovery, this work establishes a scalable plasma-amination platform for engineering molecular-sieving pore architectures, offering a generalizable principle for designing humidity-tolerant membranes.
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Liu et al. (2026) studied this question.
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