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Updated: May 20, 2025

Stable Aqueous Suspensions of Manganese Ferrite Clusters with Tunable Nanoscale Dimension and Composition
Published on: February 5, 2022
Impact of organic carbon-Mn oxide interactions on colloid stability and contaminant metals in aquatic environments
Qianqian Li1, Debra M Hausladen1
1Department of Civil and Building Engineering, Université de Sherbrooke, Quebec J1K 2R1, Canada.
Abstract:
Interactions between organic carbon and Mn oxides can lead to the formation of C-Mn colloids, which play a crucial role in regulating Mn mobility in the environment. Despite the significance of these interactions, the impact of C-Mn oxide interactions on the mobility of these colloids, particularly in the presence of contaminant metals, remains poorly understood. This study investigated the aggregation kinetics of C-Mn colloids formed through the reaction between humic acid and Mn oxides at three C:Mn molar ratios in the presence of divalent cations (Ca2+ and Mg2+). The introduction of organic carbon increased the stability (i.e., ability to resist aggregation) of C-Mn colloids compared to pure Mn(IV) colloids, as reflected in the higher critical coagulation concentration (CCC). As C:Mn molar ratios rose from 0.5 to 3 during colloid formation, the CCCs for the resulting C-Mn colloids increased from 3.6 mM to 7.2 mM Ca2+. However, at the highest C:Mn ratio (C:Mn=15), the CCCs decreased slightly to 7.0 mM Ca2+, with a similar trend observed for Mg2+. The stability of C-Mn colloids was affected by characteristics including electrostatic repulsion, surface functional groups, and Mn(II) content, resulting from reaction with dissolved organic carbon. Based on CCCs, C-Mn colloids were most stable in the presence of Mn2+ (6.9 mM), followed by Co2+ (5.9 mM), Zn2+ (2.7 mM), and Cd2+ (1.9 mM). The capacity of contaminant metals to destabilize C-Mn colloids followed the reverse order, with Cd2+ having the greatest destabilizing effect. Variations among the metals were influenced by factors such as atomic radius, hydration shell, electronegativity, and electrostatic repulsion. These results provide new insight into the aggregation behavior of C-Mn colloids and the mechanisms controlling the fate and mobility of associated contaminant metals. This knowledge has important implications for understanding contaminant transport in natural waters and optimizing water treatment processes.
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