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New lead-vanadate based sorbents were synthesized with the aim to entrap and confine gaseous iodine in off-gas streams coming from reprocessing facilities of spent nuclear fuel. Their synthesis relies on the shaping of a lead-vanadate, lead sulfide and alginic acid mix as millimetric beads. These beads were calcined between 220°C and 500°C to remove organic alginic compounds template. However, according to the calcination temperature, lead sulfide could be partially oxidized, limiting iodine loading capacity. A compromise temperature between 290°C and 350°C was found to remove most of the alginic acid template and avoiding lead sulfide oxidation. These sorbents were tested for iodine trapping in static conditions at 60°C. They performed well with a sorption capacity up to 155 mg.g−1 by forming PbI2. Furthermore, these iodine-loaded sorbents could be easily converted into an iodine-containing lead-vanadate apatite matrix by spark plasma sintering. A dense sample was produced for a sintering temperature of 500°C under 70 MPa. Such a material could be suitable for radioactive iodine conditioning in deep geological disposal. Finally, lead-vanadate sorbents could provide an easy way to entrap and confine radioactive iodine from off-gas streams into a durable material within a few steps.

A number of diazapolycyclic structures obtained by cycloaddition reaction of benzo[g]phthalazine-1,4-dione with several 1,3-dienes have been catalytically hydrogenated on palladium over charcoal. In a first step the double bond formed in the cycloaddition was reduced, except in the case of tetrasubstitution. The use of longer reaction times led to the selective reduction of the terminal aromatic rings, although the presence of the 5-methoxy substituent favored tetrahydropyridazine ring opening and prevented aromatic ring reduction. The stereochemical features of new compounds obtained are commented on the basis of X-ray and nmr data.

Synthese des derives nitro, hydroxy, methoxy-6 du compose du titre a partir de l'acide naphtalenedicarboxylique-2,3; leur reaction avec des derives du butadiene-1,3 conduit aux tetrahydro-1,4,6,13 benzo [g] pyridazino [1,2-b] phtalazinediones-6,13 substitues en 8; reduction des derives nitro-8 en derives amino-8

Synthese de bis-[hydroxy-, methoxy- et dimethylamino-3 propylamino]-1,4 benzo [g] phtalazines a partir de dichloro-1,4 benzo [g] phtalazines et des propylamines correspondantes (obtention egalement des derives monosubstitues). Activite anticancereuse