摘要
Glyphosate, the most widespread organophosphorus herbicide, enters lakes, rivers and groundwater through rainwater and surface runoff. It is very important to remove glyphosate from neutral water bodies. A new strategy for the development of glyphosate adsorbent was implemented through in situ nanoconfinement of hydrated ferric oxide (Fe 2 O 3 ·nH 2 O) in an anion exchange resin D201 (D201/Fe 2 O 3 ·nH 2 O). Fe 2 O 3 ·nH 2 O was confined within the 12–140 nm pores of D201/Fe 2 O 3 ·nH 2 O, exhibiting uniform distribution, nanoscale and amorphous state. Benefiting from the cross-linked polystyrene network, D201/Fe 2 O 3 ·nH 2 O featured excellent chemical stability in weakly acidic (pH > 3), alkaline and salt solutions. Compared with its host D201, D201/Fe 2 O 3 ·nH 2 O exhibited larger rate constant k 1 , larger glyphosate capacity and superior selectivity at pH = 7.0 ± 0.05. Corresponding its bifunctional groups of -N + (CH 3 ) 3 and Fe 2 O 3 ·nH 2 O, D201/Fe 2 O 3 ·nH 2 O could adsorb glyphosate through the two mechanisms of the ligand exchange between glyphosate anion and hydroxyl group, as well as the anion exchange between Cl − and glyphosate anion. D201/Fe 2 O 3 ·nH 2 O showed the commendable reusability and maintained constant glyphosate adsorption capacities at 161.5–164.5 mg/g in five consecutive adsorption-regeneration cycles. At the injection glyphosate concentration of 1.1 mg/mL, the effective processing volumes of D201/Fe 2 O 3 ·nH 2 O were 3.81 and 3.21 times that of D201 at two breakthrough points.
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