Zerovalent iron (Fe0, ZVI) has drawn great interest as an inexpensive and effective material to promote the degradation of environmental contaminants. A focus of ZVI research is to increase degradation kinetics and overcome passivation for long-term remediation. Halide ions promote corrosion, which can increase and sustain ZVI reactivity. Adding chloride or bromide salts with Fe0 (1% w/v) greatly enhanced TNT, RDX, and HMX degradation rates in aqueous solution. Adding Cl or Br salts after 24 h also restored ZVI reactivity, resulting in complete degradation within 8 h. These observations may be attributed to removal of the passivating oxide layer and pitting corrosion of the iron. While the relative increase in degradation rate by Cl- and Br- was similar, TNT degraded faster than RDX and HMX. HMX was most difficult to remove using ZVI alone but ZVI remained effective after five HMX reseeding cycles when Br- was present in solution. The addition of halide ions promotes the degradation of high explosives by zerovalent iron.

The monitoring of a spring and seven piezometers in the 3 km2 Brévilles agricultural catchment (France) over five and a half years revealed considerable spatial and temporal variability in the concentrations of atrazine and its metabolite deethylatrazine (both systematically quantified at the outlet spring): maximum 0.97 and 2.72 μg L-1, mean 0.19 and 0.59 μg L-1, respectively. Isoproturon, the pesticide applied in the greatest amount, was detected in only 10 of the 133 samples. These observations can only partly be explained by land use and intrinsic pesticide properties. Geochemical measurements and tritium dating showed the importance of the stratification of the sandy saturated zone and the buffer function of the unsaturated limestone. Principal component analysis on 39 monthly data series of atrazine, deethylatrazine, nitrate, chloride and piezometric levels revealed a temporal structuring of the data possibly reflecting the existence within the aquifer of two different reservoirs with time-variable contributions. We present an integrated approach combining geochemistry and hydrogeology that leads to a better understanding of the spatial and temporal fluctuations of the pesticide concentrations in groundwater of a pilot agricultural catchment.

A comparison was made of the ability of three different methods to describe the deposition and distribution of chloride from deicing salt in the roadside environment along a highway: direct sampling of airborne deposition (including snow ploughing) in containers; soil sampling and analysis of chloride content in the topsoil; and direct current resistivity measurements. Each method showed a distribution with significant decreasing values with increasing distance from the road. Two transport mechanisms, splash and spray, were identified when describing the airborne deposition. A mathematical model that includes these two transport mechanisms was adopted, and the total amount of airborne deposition on the ground 0–100 m from the road was estimated to approximately 45% of the salt applied on the road. The main part of the chloride spread by air and ploughing ended up within 10 m from the road. The soil sampling and resistivity measurements also showed the highest impact within this distance. The variation in chloride content in the soils reflected a poorer drainage ability of fine-grained soils compared to more coarse-grained soils. The resistivity measurements represented an integrated value of the differences in geology, water content and salinity. The increase in resistivity with distance from road in the topsoil was interpreted to reflect the distribution of chloride from deicing salt.

Fluxes of principal anions and cations with bulk and throughfall deposition during the growing period (April-September) were investigated for three years (2001-2003) at three sites differently exposed to the second biggest Lithuanian city - Kaunas. Fluxes of all investigated anions (SO₄ ²-, NO₃ - and Cl-) and most cations were found to be the highest in suburban area to compare with both - Rural and urban sites. The highest seasonal variability of monthly ion fluxes and the highest differences between throughfall and bulk fluxes (net throughfall) were recorded in suburban area. The highest throughfall enrichment by sulphur was detected in spring and the beginning of summer (April, May) in urban and especially in suburban sites. For nitrogen compounds (NO₃ -, NH₄ ⁺) positive net throughfall values were characteristic for urban and suburban sites and negative for rural site almost during the entire growing period. Uptake of NH₄ ⁺ ions was detected to be much higher of that for nitrates in rural area (46% vs. 22%). The most intensive enrichment of throughfall fluxes by K⁺ ions took place during the summer time (May, June, July), however, intensity of potassium leaching at the same amount of precipitation was the highest in suburban area.