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Glyphosate sorption/desorption on biochars – interactions of physical and chemical processes
Author(s) -
Hall Kathleen E,
Spokas Kurt A,
Gamiz Beatriz,
Cox Lucia,
Papiernik Sharon K,
Koskinen William C
Publication year - 2018
Publication title -
pest management science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.296
H-Index - 125
eISSN - 1526-4998
pISSN - 1526-498X
DOI - 10.1002/ps.4530
Subject(s) - biochar , sorption , glyphosate , desorption , pyrolysis , chemistry , environmental chemistry , soil water , raw material , adsorption , agronomy , organic chemistry , environmental science , soil science , biology
BACKGROUND Biochar, a carbon‐rich product of biomass pyrolysis, could limit glyphosate transport in soil and remediate contaminated water. The present study investigates the sorption/desorption behavior of glyphosate on biochars prepared from different hardwoods at temperatures ranging from 350 to 900 °C to elucidate fundamental mechanisms. RESULTS Glyphosate (1 mg L −1 ) sorption on biochars increased with pyrolysis temperature and was highest on 900 °C biochars; however, total sorption was low on a mass basis (<0.1 mg g −1 ). Sorption varied across feedstock materials, and isotherms indicated concentration dependence. Biochars with a greater fraction of micropores exhibited lower sorption capacities, and specific surface groups were also found to be influential. Prepyrolysis treatments with iron and copper, which complex glyphosate in soils, did not alter biochar sorption capacities. Glyphosate did not desorb from biochar with CaCl 2 solution; however, up to 86% of the bound glyphosate was released with a K 2 HPO 4 solution. CONCLUSION Results from this study suggest a combined impact of surface chemistry and physical constraints on glyphosate sorption/desorption on biochar. Based on the observed phosphate‐induced desorption of glyphosate, the addition of P‐fertilizer to biochar‐amended soils can remobilize the herbicide and damage non‐target plants; therefore, improved understanding of this risk is necessary. © 2017 Society of Chemical Industry

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