Lev Filippov

Stabilization of NaCl-containing cuttings wastes in cement concrete by in situ formed mineral phases.

Disposal of NaCl-containing cuttings is a major environmental concern due to the high solubility of chlorides. The present work aims at reducing the solubility of chloride by encapsulation in low permeability matrix as well as lowering its solubility by trapping into low-solubility phases. Both the studied materials were cuttings from an oil-based mud in oil drillings containing about 50% of halite, and cuttings in water-based mud from gas drilling containing 90% of halite. A reduction in the amount of dissolved salt from 41 to 19% according to normalized leaching tests was obtained by addition of potassium ortho-phosphate in the mortar formula of oil-based cuttings, while the aluminium dihydrogeno-phosphate is even more efficient for the stabilization of water-based cuttings with a NaCl content of 90%. Addition of ortho-phosphate leads to form a continuous and weakly soluble network in the cement matrix, which reduces the release of salt. The formed mineralogical phases were apatite and hydrocalumite. These phases encapsulate the salt grains within a network, thus lowering its interaction with water or/and trap chloride into low-solubility phases. The tested approaches allow to develop a confinement process of NaCl-containing waste of various compositions that can be applied to wastes, whatever the salt content and the nature of the drilling fluids (water or oil).

Synthesis of potassium ferrate using residual ferrous sulfate as iron bearing material

This paper summarizes the results obtained during potassium ferrate (K2FeVIO4) synthesis which is a high added value material. This compound that contains iron in the rare hexavalent state is becoming a substance of growing importance for the water and effluent treatment industries. This is due to its multi-functional nature (oxidation, flocculation, elimination of heavy metals, decomposition of organic matter, etc.). The most well known synthesis methods for potassium ferrate synthesis are those involving the chemical and/or electrochemical oxidation of iron (II) and (III) from aqueous solutions having a high alkali concentration. These methods are generally characterized by a low FeVI efficiency due to the reaction of the potassium ferrate with water, leading to the reduction of FeVI into FeIII. Concerning the work pertinent to this paper, the synthesis of K2FeVIO4 was achieved by a simultaneous reaction of two solids (iron sulfate and KOH) and one gaseous oxidant (chlorine). The synthesis process is performed in a rotary reactor at room temperature and the global synthesis reaction is exothermic. The effects of different experimental parameters on the potassium ferrate synthesis are investigated to determine the optimal conditions for the process.