Molecular Cages May Lower Carbon Footprint Of Chemical Separations

Dec. 4, 2020
Research from KAUST suggests molecular cages could cut the environmental impact of separating mixtures of industrial chemicals.

Molecular cages, in which guest molecules cling to the cages' outer surfaces rather than enter an internal cavity, could cut the environmental impact of separating mixtures of industrial chemicals, research from King Abdullah University of Science & Technology (KAUST) suggests. Molecular separations performed at scale by the chemical industry collectively account for as much as 15% of global energy consumption, according to KAUST. One of the most energy-intensive separations involves benzene derivatives, called xylenes, which are produced as a mixture of three isomeric forms that must be separated for their various industrial uses. The most valuable isomer, para-xylene, is a key ingredient in polyester and polyethylene terephthalate (PET) polymer manufacture.

"Conventionally, these isomers are separated by energy-demanding methods, such as fractional crystallization," says Basem Moosa, a research scientist in Niveen Khashab's lab. "Alternative techniques that require less heat would lower the carbon footprint and overall pollution of xylene separation."

Khashab and her team have been investigating the possibility of separating xylene isomers using cage-like materials, which selectively absorb one xylene isomer in the mixture, as an energy-efficient alternative separation technique. Previous research has focused on porous inorganic materials called zeolites, but processing challenges and zeolites' limited selectivity have somewhat restricted their adoption by industry.

In their latest work, KAUST researchers turned to stable, easily made organic cage materials that incorporated nitrogen-based azo groups in their structure. The materials captured the para-xylene isomer with high selectively. "Compared with other organic materials, it showed one of the highest adsorbents for xylene separations," says Aliyah Fakim, a Ph.D. student in Khashab's team. Strikingly, however, the para-xylene adsorption did not involve the isomer entering the azo-cage. Instead, the isomer stuck to the outside of the cage, forming crystals in which each para-xylene molecule was surrounded by four cage molecules.

The team plans to refine the performance of the nonporous organic cages by lowering the activation temperature and reducing the time it takes to absorb and then release the para-xylene once extracted from the mixture. However, the concept of separation using nonporous organic cages could be adopted for many industrial-scale chemical separations, lowering the energy demand of these major industrial processes, Khashab notes.

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