RESUMO
Downsizing zeolite crystals is a rational solution to address the challenge of slow adsorption rates for industrial applications. In this work, we report an environmentally friendly seed-assisted method for synthesizing nanoscale zeolite P, which has been shown to be promising for binary separations. The potassium-exchanged form of nanoagglomerates demonstrates dramatically enhanced CO2 adsorption capacity, improved diffusion rate, and separation performance. Single-component CO2 adsorption at equilibrium demonstrated higher CO2 uptake and faster adsorption kinetics (ca. 1400 s vs >130000 s) for nanosized zeolite (KP1) compared to its micron-sized (KP2) counterpart. The diffusion kinetics analysis revealed the relation between the crystal size and the transport mechanism. The micron-sized KP2 sample was primarily governed by a surface barrier resistance mechanism, while in KP1, the diffusion process involved both intracrystalline and surface barrier resistance, facilitating the surface diffusion process and enhancing the overall diffusion rate. Breakthrough curve analysis confirmed these findings as fast and efficient CO2/N2 and CO2/CH4 separations recorded for the nanosized sample. The results showed remarkably enhanced breakthrough time for KP2 vs KP1 in CO2/N2 (1.0 vs 10.9 min) and CO2/CH4 (1.1 vs 9.9 min) mixtures, along with much higher adsorption capacity for CO2/N2 (0.18 vs 1.33 mmol/g) and CO2/CH4 (0.18 vs 1.21 mmol/g) mixtures. The set of experimental data demonstrates the importance of zeolite crystal engineering for improving the gas separation performance of processes involving CO2, N2, and CH4.
