129795-76-2Relevant academic research and scientific papers
A facile precursor route to transition metal molybdates using a polyzwitterionic matrix bearing simultaneously charged moieties and complexing groups
Rullens, Francois,Deligne, Nicolas,Laschewsky, Andre,Devillers, Michel
, p. 1668 - 1676 (2005)
An unconventional but easily accessible precursor route involving the thermal treatment of hybrid precursors containing an ampholytic polymer matrix is developed to prepare multimetallic oxides of catalytic interest such as transition metal molybdates. A copolymer of diallyldimethylammonium chloride and a functionalized maleamic acid bearing an amine group suited for cation complexation was designed, synthesized and used as a matrix to stabilize inorganic species generated in solution from Ni(NO3) 2·6H2O, Co(NC3)2· 6H2O and/or Mn(NO3)2·4H2O together with (NH4)6Mo7O24· 4H2O. UV-vis-NIR as well as 13C-NMR studies suggest that the interactions between the cations and the polymer in solution are mainly electrostatic. Only minor complexation interactions take place under certain conditions. Homogeneous hybrid blends were prepared from these solutions. The presence of a complexing amine group in addition to the charged betaine moieties in the polymer permits stabilization of more than stoichiometric amounts of the metal species in the blends. XRD measurements suggest that the homogeneity in the solid state can be kept up to about 1.5 mol of each metal that is incorporated (anionic as well as cationic) per mol of repeat units of the copolymer. The blends were calcined under air at 600°C to produce the simple as well as mixed nickel, cobalt and manganese molybdates. Characterization of the final phases by XRD and Raman spectroscopy indicates that the α- as well as the β-molybdate phases can be prepared, and that the mixed structures are solid solutions of the simple NiMoO4, MnMoO 4 and CoMoO4 If the precursors engaged are homogeneous, the pH of the precursor solution, the amount of metal that is incorporated in the matrix, and the nature of the polymer matrix seem to exert only a minor influence on the nature of the final phase, which demonstrates the versatility and facile applicability of the method. The Royal Society of Chemistry 2005.
