A single-ligand ultra-microporous MOF for precombustion CO2 capture and hydrogen purification

Sci Adv. 2015 Dec 18;1(11):e1500421. doi: 10.1126/sciadv.1500421. eCollection 2015 Dec.

Abstract

Metal organic frameworks (MOFs) built from a single small ligand typically have high stability, are rigid, and have syntheses that are often simple and easily scalable. However, they are normally ultra-microporous and do not have large surface areas amenable to gas separation applications. We report an ultra-microporous (3.5 and 4.8 Å pores) Ni-(4-pyridylcarboxylate)2 with a cubic framework that exhibits exceptionally high CO2/H2 selectivities (285 for 20:80 and 230 for 40:60 mixtures at 10 bar, 40°C) and working capacities (3.95 mmol/g), making it suitable for hydrogen purification under typical precombustion CO2 capture conditions (1- to 10-bar pressure swing). It exhibits facile CO2 adsorption-desorption cycling and has CO2 self-diffusivities of ~3 × 10(-9) m(2)/s, which is two orders higher than that of zeolite 13X and comparable to other top-performing MOFs for this application. Simulations reveal a high density of binding sites that allow for favorable CO2-CO2 interactions and large cooperative binding energies. Ultra-micropores generated by a small ligand ensures hydrolytic, hydrostatic stabilities, shelf life, and stability toward humid gas streams.

Keywords: CO2 self-diffusivity; Hydrogen purification; Metal Organic Framework; Single-ligand MOF; Ultra-microporous; mixed-gas adsorption simulation; positron annihilation lifetime spectroscopy of MOF; pre-combustion CO2 capture.