<p>The applicability of the environmentally friendly MIL-100(Fe) metal-organic framework is explored for the recovery of unreacted monomers from nitrogen-rich vent streams generated in the two highest-volume thermoplastics industries: polyethylene and polypropylene. Adsorption equilibrium isotherms for ethylene and propylene were measured at multiple temperatures and fitted using the Langmuir model. Breakthrough experiments were conducted for ethylene/nitrogen and propylene/nitrogen mixtures using a bench-scale fixed-bed unit. Simulations using a dynamic fixed-bed model accurately reproduced the experimental data, validating both the kinetic and multicomponent equilibrium behavior of the system. Industrial-scale Pressure Swing Adsorption (PSA) and Multitubular Temperature and Pressure-Swing Adsorption (MT-TPSA) separation systems were designed, and evaluated. For ethylene recovery, a three-column PSA cycle operating between 0.3 and 9&#xa0;bar at 343&#xa0;K is recommended. This system achieved a productivity of 2.23&#xa0;mol/(kg·h) and a recovery capacity of 21.0&#xa0;kg C₂H₄/(m³·h) with a total energy consumption of 10.13&#xa0;MJ/kg<sub>C2H4</sub>. For propylene recovery, both a PSA cycle (0.3–8&#xa0;bar, 343&#xa0;K) and a MT-TPSA cycle (1–5&#xa0;bar, 303–393&#xa0;K) are considered. The MT-TPSA process offered higher productivity (6.72&#xa0;mol/(kg·h)) and recovery capacity (38.9&#xa0;kg C₃H₆/(m³·h)), though at a higher total energy cost of 7.46&#xa0;MJ/kg C₃H₆ compared to 4.37&#xa0;MJ/kg C₃H₆ for PSA, with a productivity of 1.48&#xa0;mol/(kg·h) and recovery capacity of 21.03&#xa0;kg C₃H₆/(m³·h).</p>

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Enhancing light olefin recovery using eco-friendly MIL-100(Fe) adsorptive processes

  • Paulo Carmo,
  • Ana M. Ribeiro,
  • Alírio E. Rodrigues,
  • Alexandre Ferreira

摘要

The applicability of the environmentally friendly MIL-100(Fe) metal-organic framework is explored for the recovery of unreacted monomers from nitrogen-rich vent streams generated in the two highest-volume thermoplastics industries: polyethylene and polypropylene. Adsorption equilibrium isotherms for ethylene and propylene were measured at multiple temperatures and fitted using the Langmuir model. Breakthrough experiments were conducted for ethylene/nitrogen and propylene/nitrogen mixtures using a bench-scale fixed-bed unit. Simulations using a dynamic fixed-bed model accurately reproduced the experimental data, validating both the kinetic and multicomponent equilibrium behavior of the system. Industrial-scale Pressure Swing Adsorption (PSA) and Multitubular Temperature and Pressure-Swing Adsorption (MT-TPSA) separation systems were designed, and evaluated. For ethylene recovery, a three-column PSA cycle operating between 0.3 and 9 bar at 343 K is recommended. This system achieved a productivity of 2.23 mol/(kg·h) and a recovery capacity of 21.0 kg C₂H₄/(m³·h) with a total energy consumption of 10.13 MJ/kgC2H4. For propylene recovery, both a PSA cycle (0.3–8 bar, 343 K) and a MT-TPSA cycle (1–5 bar, 303–393 K) are considered. The MT-TPSA process offered higher productivity (6.72 mol/(kg·h)) and recovery capacity (38.9 kg C₃H₆/(m³·h)), though at a higher total energy cost of 7.46 MJ/kg C₃H₆ compared to 4.37 MJ/kg C₃H₆ for PSA, with a productivity of 1.48 mol/(kg·h) and recovery capacity of 21.03 kg C₃H₆/(m³·h).