Insights into Paraben Adsorption by Metal-Organic Frameworks for Analytical Applications

Abstract

Metal-organic frameworks (MOFs) are attractive materials used as sorbents in analytical microextraction applications for contaminants of emerging concern (CECs) from environmental liquid matrices. The demanding specs for a sorbent in the analytical application can be comprehensively studied by considering the interactions of the target analytes with the frameworks by the use of single-crystal X-ray diffraction, computational analysis, and adsorption studies, including the kinetic ones. The current study intends a better understanding of the interactions of target CECs (particularly, propylparaben (PPB) as a model) and three Zn-based layered pillared MOFs:CIM-81[Zn2(tz)2(bdc)] (Htz = 1,2,4-triazole and H2bdc = 1,4-benzenedicarboxylic acid) and their amino derivatives [Zn2(NH2-tz)2(bdc)]CIM-82and [Zn2(tz)2(NH2-bdc)]CIM-83(NH2-Htz = 3-amino-1,2,4-triazole and NH2-H2bdc = 2-amino-1,4-benzenedicarboxylic acid). The crystal structures of the two solvate compounds (dma@CIM-81(dma = dimethylacetamide) andacetone@CIM-81) were solved by single-crystal X-ray diffraction to determine the points of interaction between the framework and the guest molecules. They also served as a starting point for the computational modeling of thePPB@CIM-81compound, showing that up to two PPB molecules can be hosted in one of the pores, while only one can be trapped in the second pore type, leading to a maximum theoretical capacity of 291.9 mg g-1. This value is close to the value obtained by the adsorption isotherm experiment forCIM-81(283 mg g-1). This value is, by far, higher than those previously reported for other materials for the removal of PPB from water, and also higher than the experimental values obtained forCIM-82(54 mg g-1) andCIM-83(153 mg g-1). The kinetics of adsorption is not very fast, with uptake of about 40% in 3 h, although a 70% release in methanol is achieved in 1 h. In addition, a further comparison of performance in analytical microextraction (requiring only 10 mg ofCIM-81) was carried out together with chromatographic analysis to support all insights attained, with the method being able to monitor CECs as low as μg L-1levels in complex environmental water samples, thus performing successfully for water monitoring even in multicomponent scenarios.