Three processing routes have been used to prepare barium titanate powders,
namely conventional coprecipitation, single-microemulsion coprecipitation u
sing diether oxalate as the precipitant, and double-microemulsion coprecipi
tation using oxalic acid as the precipitant. A single-phase perovskite bari
um titanate was obtained when the double-microemulsion-derived oxalate prec
ursor was calcined for 2 h at a temperature of as low as 550 degrees C, com
pared to 600 degrees C required by the single-microemulsion-derived precurs
or. A calcination for 2 h at >700 degrees C was required for the convention
ally coprecipitated precursor in order to develop a predominant barium tita
nate phase. It was, however, impossible to eliminate the residual TiO2 impu
rity phase by raising the calcination temperature, up to 1000 degrees C. Th
e microemulsion-derived barium titanate powders also demonstrated much bett
er powder characteristics, such as more refined crystallite and particle si
zes and a much lower degree of particle agglomeration, than those of the co
nventionally coprecipitated powder, although they contained similar to 0.2
wt% BaCO3 as the impurity phase.