Two fly ashes from municipal solid waste incineration were selected to study their heavy metal leaching behavior. The main purpose of this research is to investigate the characteristics of fly ashes and compare the leaching of heavy metals in different leaching environment. pH and acid neutralization capacity analysis showed that fly ashes were highly alkaline. Fly ashes also contained a variety of heavy metals including Pb, Cu, Cr, Zn, Cd and Ni etc. Leaching studies showed that the alkalinity of fly ashes raised the pH of leaching solution from acidic to basic. Ni, Cu and Zn were strongly bound to ashes and manifested low leaching. In contrast, Cr and Cd had high mobility but their leaching was inhibited by the low solubility of carbonate Cr and Cd. Pb was highly leachable in the alkaline environment with concentration in the leaching solution reached as high as 9.74 mg/L. In addition, the presence of EDTA in the environment also increased leaching. Pb concentration was raised to 16.63 mg/L. This could be attributed to the chelating capacity of EDTA which means that the presence of organics in natural environment should be taken into consideration.

The production rate of industrial and agricultural waste is increasing due to population growth. Soil is the most important receiver of industrial and agricultural waste. Contaminants such as heavy metals in various waste after reception by the soil, immediately become part of the cycle that has different impacts on the environment. Geopolymer, as a chemical stabilizer has the potential to stabilize heavy metals in the soil. In this research, several geopolymers for the stabilization of heavy metals in soil were synthesized. Silicon dioxide (SiO2) and aluminosilicate (Al2SiO4) must be used to produce the geopolymers. Rice husk ash was used as the SiO2 source. Also, Iranian zeolite and sepiolite, and red clay soil were utilized as the source of Al2SiO4. The synthesized geopolymers were investigated for the adsorption of nickel and cadmium. Also, batch and column studies of using geopolymers for the chemical stabilization of heavy metals in soil were conducted. The results revealed a high adsorption capacity of the geopolymers. The zeolite, sepiolite, and red clay geopolymer-soil samples adsorbed 100% of the heavy metals (i.e., Ni and Cd) at a concentration of 100 ppm. The zeolite geopolymer adsorbent adsorbed 57% and 96% of Ni and Cd at a concentration of 1000 ppm, respectively. In general, it was concluded that the use of geopolymer compounds in soils with high heavy metal adsorption capacity could be an efficient approach to prevent groundwater resource pollution.

A simple approach for ranking the leaching of pesticides from surface soil presented and tentatively calibrated with field data from an agricultural a The approach is based on the calculation of a leaching index indicating the proportion of active ingredient, with respect to the quantity applied, leac from a soil model in a given time interval (one year). In the selected area wells tapping an unconfined aquifer were sampled for groundwater pesticide residue analysis, in order to explore the index region between leachers and nonleachers.

International audience | Stabilization of soil contaminated with trace elements is a remediation practice that does not reduce the total content of contaminants, but lowers the amounts of mobile and bioavailable fractions. This study evaluated the efficiency of Fe0 to reduce the mobility and bioavailability of Cr, Cu, As and Zn in a chromated copper arsenate (CCA)-contaminated soil using chemical, biochemical and biotoxicity tests. Contaminated soil was stabilized with 1% iron grit. This treatment decreased As and Cr concentrations in leachates (by 98% and 45%, respectively), in soil pore water (by 99% and 94%, respectively) and in plant shoots (by 84% and 95%, respectively). The stabilization technique also restored most of analyzed soil enzyme activities and reduced microbial toxicity, as evaluated by the BioTox™ test. After stabilization, exchangeable and bioaccessible fractions of Cu remained high, causing some residual toxicity in the treated soil

[Departement_IRSTEA]Eaux [TR1_IRSTEA]ARCEAU | The purpose of this work is to assess the effectiveness of two grass covers (buffer zone and grass-covered inter-row), to reduce pesticide leaching, and subsequently to preserve groundwater quality. Lower amounts of pesticides leached through grass-cover soil columns (2.7e24.3% of the initial amount) than the bare soil columns (8.0e55.1%), in correspondence with their sorption coefficients. Diuron was recovered in higher amounts in leachates (8.9e32.2%) than tebuconazole (2.7e12.9%), in agreement with their sorption coefficients. However, despite having a sorption coefficient similar to that of diuron, more procymidone was recovered in the leachates (10.2e55.1%), probably due to its facilitated transport by dissolved organic matter. Thus even in this very permeable soil, higher organic matter contents associated with grass-cover reduce the amount of pesticide leaching and limit the risk of groundwater contamination by the pesticides. The results of diuron and tebuconazole transfer through undisturbed buffer zone soil columns are in agreement with field observations on the buffer zone.

International audience | Biocides are added to or applied on building materials to prevent microorganisms from growing on their surface or to treat them. They are leached into building runoff and contribute to diffuse contamination of receiving waters. This review aimed at summarizing the current state of knowledge concerning the impact of biocides from buildings on the aquatic environment. The objectives were (i) to assess the key parameters influencing the leaching of biocides and to quantify their emission from buildings; (ii) to determine the different pathways from urban sources into receiving waters; and (iii) to assess the associated environmental risk. Based on consumption data and leaching studies, a list of substances to monitor in receiving water was established. Literature review of their concentrations in the urban water cycle showed evidences of contamination and risk for aquatic life, which should put them into consideration for inclusion to European or international monitoring programs. However, some biocide concentration data in urban and receiving waters is still missing to fully assess their environmental risk, especially for isothiazolinones, iodopropynyl carbamate, zinc pyrithione and quaternary ammonium compounds, and little is known about their transformation products. Although some models supported by actual data were developed to extrapolate emissions on larger scales (watershed or city scales), they are not sufficient to prioritize the pathways of biocides from urban sources into receiving waters during both dry and wet weathers. Our review highlights the need to reduce emissions and limit their transfer into rivers, and reports several solutions to address these issues.