The performance of amended micrometric iron particles (FeB0) in trimetallic systems for the removal of aqueous diclofenac (DF) was investigated. Tested additive metals were Pd, Cu and Ni. Trimetallic systems were shown superior to Fe-0 for aqueous DF removal both under oxic and anoxic conditions. The extent of OF removal varied with (i) the combination of the additives, (ii) the order of plating on Fe-0 surface, (iii) the availability of dissolved oxygen and (iv) the presence of MnO2. In comparison with previous results for bimetallic systems: (i) DF reduction products were observed under anoxic conditions for all trimetallic systems and only in some bimetallic systems; and (ii) under oxic conditions. DF reaction products were only observed in CuPdFe system. This was accredited to the intrinsic and electronic properties of the involved metals. Rapid DF removal was mainly attributed to the capacity of additive metals to accelerate Fe-0 corrosion and thus producing more atomic hydrogen within the porous iron oxide layers. This promoted catalytic hydrodehalogenation was clearly apparent in systems where reductive transformation products were identified (e.g. PcICuFe). Recycling experiments using PdCuFe showed a continuous reactivity even after 4 successive cycles under anoxic conditions, however, under oxic conditions, a serious reactivity loss was noticed. (C) 2011 Elsevier B.V. All rights reserved.