Extracellular polymeric substances (EPS) modulate adsorption isotherms between biochar and 2,2′,4,4′-tetrabromodiphenyl ether

Extracellular polymeric substances (EPS), chars and persistent organic pollutants (POPs) frequently coexist in the environment. However, a knowledge gap exists regarding their interactions. Therefore, we applied 2,2′,4,4′-tetrabromodiphenyl ether (BDE-47) as a model POP to investigate the influence of bovine serum albumin (BSA) and sodium alginate (SA) - representing protein and polysaccharide components of EPS - on POP adsorption to biochars. Surface activities of tested biochars were characterised using nuclear magnetic resonance, X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy . The adsorption capacities of BDE-47 on biochars were significantly improved by both EPS analogues: BSA at concentrations of only 5 mg L −1 and SA at 80 mg L −1 at c e  = 1 S w BDE-47 concentration. However, 80 mg L −1 BSA decreased the BDE-47 adsorption capacities on biochars at the tested BDE-47 concentrations. Chemisorption and pore filling mechanisms appeared to dominate the adsorption process of BDE-47 on maize straw and wheat straw biochars. After adding BSA (or SA), a hydrophobic partition effect was found to best explain the adsorption process and linearity of adsorption was enhanced. These results progress our understanding of bioavailability and migration of POPs: especially relevant to the water industry and biochar/EPS facilitated removal of these contaminants.