Showing posts with label Nickel. Show all posts
Showing posts with label Nickel. Show all posts

Tuesday, 11 October 2016

Copper, Chromium, Nickel, Lead and Zinc levels and pollution degree in firing rage soils

Land Degrad. Develop. 27: 1721–1730 (2016)


Small-arms firing ranges are an important source of metal contaminants in the ecosystems located near these facilities, owing to the constant fall and alteration of the ammunition remnants on the soil, particularly in nearby berms. The objectives of this study were to analyse the pollution of chromium (Cr), copper (Cu), nickel (Ni), lead (Pb) and zinc (Zn) in rifle/pistol shooting range soils, to estimate their availability and to evaluate the influence of the ammunition used. The concentrations of Pb, Zn, Cu, Cr and Ni range from 55 to 6·309, 34 to 264, 19 to 98, 40 to 79 and 11 to 33 mg kg 1, respectively. The moderate acidity and organic matter content favour the availability of Pb, followed by Cu > Zn > Ni > Cr. The values of different contamination indexes (Igeo, pollution index and integrated pollution index) suggest that Pb soil contamination is moderate to heavy, especially in the berm area and moderate for Cu and Zn. Lead ammunition is the main source of pollution, but another one was identified owing to the concentrations of Fe, Cr and Ni detected. Further studies are needed to verify their long-term potential adverse effects.

Sunday, 9 October 2016

TOF-SIMS and FE-SEM/EDS to verify the heavy metal fractionation in serpentinite quarry soils

CATENA, 136, 2016, 30–43


This study aims at extensively defining serpentinite quarry soils and analysing their content and distribution of heavy metals using chemical sequential extraction. The association with the different geochemical phases of the soil was verified using TOF-SIMS and SEM-EDS techniques. Seven soils were chosen in two serpentinite quarries located in Moeche (M) and Silleda (C) (Galicia, northwest of Spain). The selected areas for soil sampling were: dump sites (M1, M2 and C1), rock extraction sites (M3, C2), and quarry boundaries (M4 and C3). The total soil concentration of Co, Cr, Ni, and V varied from 1472 to 7132, 1499 to 4309, 76 to 373, and 21 to 140 mg kg− 1, respectively. In all cases they exceed the maximum limit permitted in soils. After chemical sequential extraction it was found that the high content of Co, Cr, Ni, and V is associated with the residual fraction of the soils. In addition, Fe and Mn oxides have a high capacity for Co fixation, whereas Cr, Ni, and V are mainly associated with magnesium silicates. The fractions related to organic matter and the soluble or available forms are, respectively low and very low, not exceeding 2.5% in any of the soils. This association of the metals with magnesium silicates and Fe oxides, and the low content of metals bound to organic matter were identified by using the TOF-SIMS and SEM-EDS techniques. Both techniques confirmed and verified the results obtained during the chemical sequential extraction by checking the interaction of heavy metals with the different components of the soil.

Saturday, 2 April 2016

Changes in Cd, Cu, Ni, Pb and Zn Fractionation and Liberation Due to Mussel Shell Amendment on a Mine Soil

Land Degradation and Development 27 (2016) 1276–1285
DOI: 10.1002/ldr.2505


Mining activities are related to relevant environmental pollution issues that should be controlled. We used sequential extractions to fractionate Cd, Cu, Ni, Pb and Zn retained on unamended or mussel shell-amended mine soil samples, all of them treated with a mixture of the five heavy metals (total metal concentration of 1·57 mmol L−1), after 1, 7 and 30 days of incubation. In addition, we used the stirred flow chamber technique to study the release of each of the five heavy metals from these different unamended and shell-amended soil samples. The results indicate that the shell amendment caused a decrease in the most soluble fraction, while increasing the most recalcitrant (least mobile) fraction. With equivalent implications, the stirred flow chamber experiments showed that mussel shell amendment was associated to a decrease in heavy metal release and increased retention. The highest mussel shell dose and incubation time caused the most relevant changes in pH values and thus in metal retention, also indicating the importance of pH modifications in the mechanism of retention acting in the amended samples. In view of these results, the use of mussel shell amendment can be encouraged to increase heavy metal retention in acid mine soils, in order to minimise risks of environmental pollution.