Carbon dioxide and hydrogen adsorption study on surface-modified HKUST-1 with diamine/triamine

Abstract

Abstract The present article intended to study the influence of post-synthetic modification with ethylenediamine ( en , diamine) and diethylenetriamine ( deta , triamine) within the coordinatively unsaturated sites (CUSs) of HKUST-1 on carbon dioxide and hydrogen storage. The as-sythesized adsorbent was solvent-exchanged and subsequently post-synthetically modified with di-/triamines as sources of amine-based sorption sites due to the increased CO 2 storage capacity. It is known that carbon dioxide molecules have a high affinity for amine groups, and moreover, the volume of amine molecules itself reduces the free pore volume in HKUST-1, which is the driving force for increasing the hydrogen storage capacity. Different concentrations of amines were used for modification of HKUST-1, through which materials with different molar ratios of HKUST-1 to amine: 1:0.05; 1:0.1; 1:0.25; 1:0.5; 1:0.75; 1:1; 1:1.5 were synthesized. Adsorption measurements of carbon dioxide at 0 °C up to 1 bar have shown that the compounds can adsorb large amounts of carbon dioxide. In general, deta -modified samples showed higher adsorbed amounts of CO 2 compared to en -modified materials, which can be explained by the higher number of amine groups within the deta molecule. With an increasing molar ratio of amines, there was a decrease in wt.% CO 2 . The maximum storage capacity of CO 2 was 22.3 wt.% for HKUST-1: en /1:0.1 and 33.1 wt.% for HKUST-1: deta /1:0.05 at 0 °C and 1 bar. Hydrogen adsorption measurements showed the same trend as carbon dioxide, with the maximum H 2 adsorbed amounts being 1.82 wt.% for HKUST-1: en /1:0.1 and 2.28 wt.% for HKUST-1: deta /1:0.05 at − 196 °C and 1 bar.