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A contrast variation SANS and SAXS study of soil derived dissolved organic matter, and its interactions with hematite nanoparticles

Andersson, Erika LU ; Meklesh, Viktoriia LU ; Gentile, Luigi LU ; Schweins, Ralf ; Matsarskaia, Olga ; Tunlid, Anders LU ; Persson, Per LU and Olsson, Ulf LU (2023) In JCIS Open 11.
Abstract

Soil derived dissolved organic matter (DOM) is an important component of the carbon cycle and influences numerous biogeochemical processes, including the formation of mineral-organic associations. DOM ranges in size from small organic molecules to macromolecules and colloidal aggregates. In this study we have used small angle neutron (SANS) and X-ray (SAXS) scattering to characterize the colloidal DOM fraction from the organic layer of a boreal forest soil, and its interactions with hematite (α-Fe2O3) mineral nanoparticles. Comparison between SAXS and contrast variation SANS patterns revealed that the scattering form factor of the colloidal DOM aggregates was essentially independent of the scattering contrast,... (More)

Soil derived dissolved organic matter (DOM) is an important component of the carbon cycle and influences numerous biogeochemical processes, including the formation of mineral-organic associations. DOM ranges in size from small organic molecules to macromolecules and colloidal aggregates. In this study we have used small angle neutron (SANS) and X-ray (SAXS) scattering to characterize the colloidal DOM fraction from the organic layer of a boreal forest soil, and its interactions with hematite (α-Fe2O3) mineral nanoparticles. Comparison between SAXS and contrast variation SANS patterns revealed that the scattering form factor of the colloidal DOM aggregates was essentially independent of the scattering contrast, implying that the colloidal aggregates have an essentially homogeneous chemical composition, down to the nanometre length scale. Variation of the D2O/H2O ratio of the solvent yielded a SANS intensity minimum at ca. 40 ​vol % D2O, which was consistent with colloids composed of mainly polysaccharides. At pH 5.5 the pure hematite nanoparticles were colloidally stable in water and characterized by a ζ-potential of +25 ​mV and a hydrodynamic radius of ca. 70 ​nm. In the presence of DOM, the hematite nanoparticles lost the colloidal stability and aggregated into larger clusters, displaying a negative ζ-potential of ca. −25 ​mV. The charge reversal suggested that negatively charged polyanions of DOM adsorbed onto the hematite particles, possibly leading to bridging flocculation. Our results suggested that mainly low molecular weight components induced hematite aggregation because no or very limited interactions between DOM colloids and hematite were detected.

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author
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organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Contrast variation, Cryo-TEM, Dissolved organic matter, Hematite nanoparticles, Small angle neutron scattering, Small angle X-ray scattering
in
JCIS Open
volume
11
article number
100091
publisher
Elsevier
external identifiers
  • scopus:85165294641
DOI
10.1016/j.jciso.2023.100091
language
English
LU publication?
yes
id
e2247ca1-df86-4696-8570-fa047f508370
date added to LUP
2023-08-25 12:22:37
date last changed
2023-08-29 12:27:34
@article{e2247ca1-df86-4696-8570-fa047f508370,
  abstract     = {{<p>Soil derived dissolved organic matter (DOM) is an important component of the carbon cycle and influences numerous biogeochemical processes, including the formation of mineral-organic associations. DOM ranges in size from small organic molecules to macromolecules and colloidal aggregates. In this study we have used small angle neutron (SANS) and X-ray (SAXS) scattering to characterize the colloidal DOM fraction from the organic layer of a boreal forest soil, and its interactions with hematite (α-Fe<sub>2</sub>O<sub>3</sub>) mineral nanoparticles. Comparison between SAXS and contrast variation SANS patterns revealed that the scattering form factor of the colloidal DOM aggregates was essentially independent of the scattering contrast, implying that the colloidal aggregates have an essentially homogeneous chemical composition, down to the nanometre length scale. Variation of the D<sub>2</sub>O/H<sub>2</sub>O ratio of the solvent yielded a SANS intensity minimum at ca. 40 ​vol % D<sub>2</sub>O, which was consistent with colloids composed of mainly polysaccharides. At pH 5.5 the pure hematite nanoparticles were colloidally stable in water and characterized by a ζ-potential of +25 ​mV and a hydrodynamic radius of ca. 70 ​nm. In the presence of DOM, the hematite nanoparticles lost the colloidal stability and aggregated into larger clusters, displaying a negative ζ-potential of ca. −25 ​mV. The charge reversal suggested that negatively charged polyanions of DOM adsorbed onto the hematite particles, possibly leading to bridging flocculation. Our results suggested that mainly low molecular weight components induced hematite aggregation because no or very limited interactions between DOM colloids and hematite were detected.</p>}},
  author       = {{Andersson, Erika and Meklesh, Viktoriia and Gentile, Luigi and Schweins, Ralf and Matsarskaia, Olga and Tunlid, Anders and Persson, Per and Olsson, Ulf}},
  keywords     = {{Contrast variation; Cryo-TEM; Dissolved organic matter; Hematite nanoparticles; Small angle neutron scattering; Small angle X-ray scattering}},
  language     = {{eng}},
  publisher    = {{Elsevier}},
  series       = {{JCIS Open}},
  title        = {{A contrast variation SANS and SAXS study of soil derived dissolved organic matter, and its interactions with hematite nanoparticles}},
  url          = {{http://dx.doi.org/10.1016/j.jciso.2023.100091}},
  doi          = {{10.1016/j.jciso.2023.100091}},
  volume       = {{11}},
  year         = {{2023}},
}