Immobilization of metal-humic acid complexes in anaerobic granular sludge for their application as solid-phase redox mediators in the biotransformation of iopromide in UASB reactors.

Metal-humic acid complexes were synthesized and immobilized by a granulation process in anaerobic sludge for their application as solid-phase redox mediators (RM) in the biotransformation of iopromide. Characterization of Ca- and Fe-humic acid complexes revealed electron accepting capacities of 0.472 and 0.556milli-equivalentsg(-1), respectively. Once immobilized, metal-humic acid complexes significantly increased the biotransformation of iopromide in upflow anaerobic sludge blanket (UASB) reactors. Control UASB reactor (without humic material) achieved 31.6% of iopromide removal, while 80% was removed in UASB reactors supplied with each metal-humic acid complex. Further analyses indicated multiple transformation reactions taking place in iopromide including deiodination, N-dealkylation, decarboxylation and deacetylation. This is the first successful application of immobilized RM, which does not require a supporting material to maintain the solid-phase RM in long term operation of bioreactors. The proposed redox catalyst could be suitable for enhancing the redox conversion of different recalcitrant pollutants present in industrial effluents.

Preparation of telluro- and selenoalumoxanes under mild conditions.

Syntheses of the heavy chalcogen-containing alumoxanes [(Me)LAl(SeH)]2(µ-O) (4) and ((Me)LAl)2(µ-Te)(µ-O) (7) were accomplished by the reaction of ((Me)LAlH)2(µ-O) (2; (Me)L = HC[(CMe)N(2,4,6-Me3C6H2)]2(-)) with either red selenium or metallic tellurium. The aluminum hydrogenselenide [(Me)LAl(SeH)]2(µ-Se) (3) was also prepared from the reaction of red selenium and (Me)LAlH2 (1). All compounds were characterized by spectroscopic methods and X-ray diffraction studies. Density functional theory calculations were performed on 4 and 7.