Adsorption of the hydrophobic organic pollutant hexachlorobenzene to phyllosilicate minerals

dc.contributor.authorBöhm, Leonard
dc.contributor.authorGrancic, Peter
dc.contributor.authorScholtzová, Eva
dc.contributor.authorHeyde, Benjamin Justus
dc.contributor.authorDüring, Rolf-Alexander
dc.contributor.authorSiemens, Jan
dc.contributor.authorGerzabek, Martin H.
dc.contributor.authorTunega, Daniel
dc.date.accessioned2023-11-15T11:21:34Z
dc.date.available2023-11-15T11:21:34Z
dc.date.issued2022
dc.description.abstractHexachlorobenzene (HCB), a representative of hydrophobic organic chemicals (HOC), belongs to the group of persistent organic pollutants (POPs) that can have harmful effects on humans and other biota. Sorption processes in soils and sediments largely determine the fate of HCB and the risks arising from the compound in the environment. In this context, especially HOC–organic matter interactions are intensively studied, whereas knowledge of HOC adsorption to mineral phases (e.g., clay minerals) is comparatively limited. In this work, we performed batch adsorption experiments of HCB on a set of twelve phyllosilicate mineral sorbents that comprised several smectites, kaolinite, hectorite, chlorite, vermiculite, and illite. The effect of charge and size of exchangeable cations on HCB adsorption was studied using the source clay montmorillonite STx-1b after treatment with nine types of alkali (M+: Li, K, Na, Rb, Cs) and alkaline earth metal cations (M2+: Mg, Ca, Sr, Ba). Molecular modeling simulations based on density functional theory (DFT) calculations to reveal the effect of different cations on the adsorption energy in a selected HCB-clay mineral system accompanied this study. Results for HCB adsorption to minerals showed a large variation of solid–liquid adsorption constants Kd over four orders of magnitude (log Kd 0.9–3.3). Experiments with cation-modified montmorillonite resulted in increasing HCB adsorption with decreasing hydrated radii of exchangeable cations (log Kd 1.3–3.8 for M+ and 1.3–1.4 for M2+). DFT calculations predicted (gas phase) adsorption energies (− 76 to − 24 kJ mol−1 for M+ and − 96 to − 71 kJ mol−1 for M2+) showing a good correlation with Kd values for M2+-modified montmorillonite, whereas a discrepancy was observed for M+-modified montmorillonite. Supported by further calculations, this indicated that the solvent effect plays a relevant role in the adsorption process. Our results provide insight into the influence of minerals on HOC adsorption using HCB as an example and support the relevance of minerals for the environmental fate of HOCs such as for long-term source/sink phenomena in soils and sediments.
dc.description.sponsorshipDeutsche Forschungsgemeinschaft (DFG); ROR-ID:018mejw64
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/18648
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-18012
dc.language.isoen
dc.rightsNamensnennung 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectPersistent organic pollutants (POP)
dc.subjectClay minerals
dc.subjectMontmorillonite
dc.subjectMolecular simulations
dc.subjectHalogenated aromatic hydrocarbons
dc.subjectCations
dc.subjectHydration enthalpy
dc.subjectEnvironmental fate
dc.subject.ddcddc:630
dc.titleAdsorption of the hydrophobic organic pollutant hexachlorobenzene to phyllosilicate minerals
dc.typearticle
local.affiliationFB 09 - Agrarwissenschaften, Ökotrophologie und Umweltmanagement
local.projectgrant number 443637168, BO5388/1–1
local.source.epage36837
local.source.journaltitleEnvironmental science and pollution research
local.source.spage36824
local.source.urihttps://doi.org/10.1007/s11356-022-24818-4
local.source.volume30

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