Abstract

A study of the behavior of R- and S-enantiomers of ibuprofen (R-IBU and S-IBU) in aqueous solution by nanofiltration (NF) membranes revealed that up to 23% of the pharmaceutical was adsorbed onto the stainless steel equipment of a flat-sheet experimental unit. Mass balances disclosed that IBU’s S-enantiomer was primarily responsible for the adsorption onto the equipment. Additional IBU adsorption was also experienced on the NF membrane coupons, verified by increased contact angle measurements on the surfaces. The IBU-equipment adsorptive relationship with and without the membrane coupon were best described by Freundlich and Langmuir isotherms, respectively. At a feed water pH of 4.0 units and racemic µg/L IBU concentrations, NF removal ranged from 34.5% to 49.5%. The rejection of S-IBU was consistently greater than the R-enantiomer. Adsorption onto the surfaces influenced NF rejection by 18.9% to 27.3%. The removal of IBU displayed a direct relationship with an increase in feed water pH. Conversely, the adsorption of IBU exhibited an indirect relationship with an increase in feed water pH.

Highlights

  • The existence and subsequent discovery of chemicals of emerging concern (CECs) in aquatic environments has sparked interest in determining removal capabilities of specific water treatment technologies

  • Adequate mass balance tests are recommended in bench-scale membrane filtration experiments to confirm that rejection is not affected by solute behavior such as volatilization, adsorption, or a reaction with the feed water matrix

  • The test was repeated at a feed water pH range from 3.0 to 7.0 units, resulting in an inverse relationship between loss of enantiomeric IBU and the water quality parameter, aligning with the acid dissociation constant of IBU (4.4)

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Summary

Introduction

The existence and subsequent discovery of chemicals of emerging concern (CECs) in aquatic environments has sparked interest in determining removal capabilities of specific water treatment technologies. The extent of solute removal is dependent on chemical properties, feed water matrix composition, membrane characteristics, and operational variables [1,2,6,7,8]. A strong research effort has attempted to elucidate the impact of CEC properties on solute removal through NF processes. Other solute characteristics such as chemical properties, solute geometry, and functional groups can affect rejection of CECs [1,6,7]. Correlations between CEC removal and hydrophobicity [12], membrane adsorption [13], polarizability [14], polarity [15,16], and molecular size and shape [6,7,14,17,18] have been noted. The complexities of CEC mass transfer have been scrutinized and reported on over the years and serve as the basis for additional investigations such as those presented

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