Abstract

The direct use of nanosorbents for water purification is limited due to their aggregation and the lack of techniques for their recovery from natural waters. To overcome these problems, the affixation of nanomaterials onto bulk, non-mobile supports has been proposed. However, a method to simulate the efficiency of these sorbents under realistic conditions is still not available. To address this need, this work describes a method for evaluating the sorption efficiency of nanosorbent materials incorporated on bulk supports under non-equilibrium conditions. The method combines the principles of passive sampling, an environmental monitoring technique that is based on passive diffusion of dissolved contaminants from water to a sorbent, with batch sorption experiments that measure sorption under equilibrium conditions, to determine the parameters associated with water purification. These parameters are the maximum sorption capacity of the sorbent and the sampling rate, which is the volume of contaminated water treated per unit of time. From these variables, the deployment time of the sorbent until reaching saturation is proposed as an alternative indicator of sorbent efficiency. As proof-of-principle, the removal of oxyanions from a Zr-metal-organic framework (MOR−1) immobilized on cotton textiles was investigated. The results show that the sorption capacity under passive diffusion uptake conditions, is approximately 20 mg/g for As(VI) and 36 mg/g Se(IV), which is 10 to 30 times lower compared to that determined in batch sorption studies, indicating that conventional equilibrium sorption overestimates the efficiency of the sorbents under realistic conditions. The application of the method to a worst-case scenario, involving the severe contamination of freshwaters with arsenate species, is also demonstrated.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call