Adsorption-desorption and co-migration of vanadium on colloidal kaolinite.

Vanadium (V) pollution in soil has been widely noted, while knowledge about the effect of soil colloid on migration of V is scarce. Batch adsorption-desorption and transportation of the colloid-adsorbed V in columns packed with quartz sand under various environment conditions were carried out to explore the retention and transportation of V by colloidal kaolinite. Batch adsorption-desorption studies show that the adsorption of V by the colloidal kaolinite was mainly specific adsorption and redox played a limited role in the adsorption process. The maximum adsorption capacity of the colloidal kaolinite was 712.4 mg g-1, and about 5.9-8.7% of the adsorbed V could be desorbed. Both the adsorption-desorption and migration of V with colloidal kaolinite were highly ambient condition dependent. The column studies show that V was highly mobile in the saturated porous media. An easier transfer of V with an increase in pH, IS, and velocity of flow was noted. However, the increase of IS lead to the blockage of the colloidal kaolinite transportation. The recovery rate of the colloidal kaolinite at pH 7 and 9 was 2.0 and 2.1 times that at pH 5, respectively. The migration of colloidal-adsorbed V in sand column preceded that of V ion, but more colloidal-bound V than V ion remained in the column. Lack of consideration of the combination and co-transportation of V and colloidal kaolinite will lead to an overestimation of the risk of V to deeper soil profiles and groundwater. Graphical abstract.

Characteristic of adsorption, desorption, and co-transport of vanadium on humic acid colloid.

Understanding the interactions between humic acid colloid (HAC) and vanadium (V) in soils is of great importance in forecasting the behaviors and fates of V in the soil and groundwater systems. This study investigated the characteristics and factors that affect V adsorption-desorption by the HAC; meanwhile, we also explored the co-transport of the HAC and V in a saturated porous media. Scanning Electronic Microscopy micrographs showed the variation of morphological features on the surface of the HAC before and after V adsorption. Fourier transform infrared spectroscopy spectra revealed that the presence of hydroxyl, carboxyl, carbonyl, carbon-carbon double bond, amino, and aromatic ring on the HAC participated in V adsorption. The adsorption isotherms were well described by the Langmuir model, and the adsorption kinetics of the HAC was better described by the pseudo-first-order kinetic models. The adsorption-desorption was strongly dependent on the initial V concentration, solution pH, and temperature. The maximum adsorption amount was 861.17 mg g-1 by 200 mg L-1 HAC at the initial V concentration of 500 mg L-1, and the corresponding desorption amount was 15.13 mg g-1. These results showed that the HAC had high fixation capacity of V in soil. In addition, the HAC sped up the mobility of V; however, it decreased mass of migration of V in the saturated quartz sand column. These results are expected to provide insight into the potential impact of HAC on geochemical behaviours of V in vulnerable ecosystems.

Distribution, health risk assessment, and anthropogenic sources of fluoride in farmland soils in phosphate industrial area, southwest China.

The high concentration of fluoride (F) in soils has become a rising concern for its toxicity to microbes, plants, animals and human health. In the present study, the spatial and vertical distribution, health risk assessment and anthropogenic sources of F in farmland soils in an industrial area dominated by phosphate chemical plants were studied. Concentrations of total fluoride (TF) and water soluble fluoride (WSF) in the surface soils decreased with distance within the range of 2500 m at the prevailing downwind of the industrial area. The soil TF and WSF concentrations in 0-40 cm profiles were higher than those in 40-100 cm layers in the industrial area. At the prevailing downwind of the industrial area within 700 m, the hazard quotient values of human exposure to surface soils were higher than 1, indicating that a potential risk may exist for human health in this area. The main exposure pathway for children and adults was oral ingestion and particulate inhalation, respectively. The source apportionment model of soil F was modified based on years' historical data and experimental data. The results showed that the proportion of anthropogenic sources of soil F was dustfalls (69%) > irrigation water (23%) > air (5%) > chemical fertilizers (3%) in the industrial area. The high F concentration of dustfalls was mainly due to the phosphate rock, phosphogypsum, and surface soils with high F contents from the factories. In order to safeguard human health and alleviate hazards of F to surroundings, the control of pollutants emission from factories was a basic and vital step to reduce F in the soils in industrial areas.

Vertical distribution of fluorine in farmland soil profiles around phosphorous chemical industry factories.

High concentration of fluorine (F) in agricultural soils has got significant attention considering its impacts on human health, but little information was available about F distribution in farmland soil profiles around phosphorous chemical industry factories. In present study, farmland soil profiles and relevant medium samples were collected from farmlands around a main phosphorous chemical base in southwest China. At 0-100-cm profiles, concentrations of soil total F (Ft, 400.9-1612.0 mg kg-1) and water soluble F (Fw, 3.4-26.0 mg kg-1) decreased with profile depth in industrial areas. Industrial activities enhanced F concentration in soil mainly at 0-40-cm profiles. No disparity for both Ft and Fw distributions in paddy-dry land rotation field and dry land indicates short-term land utilization could not affect the F distribution in soil profiles. Correlation analysis showed soil organic matter and wind direction were important factors influencing the distribution of F in soil profiles. The shutdown of factory and government control of industrial emissions effectively decreased the ambient air F (Fa) concentrations in industrial areas. In where Fa and dustfall F concentrations were high, high soil Ft, Fw, and crop edible part F concentrations were found.