A flow injection spectrophotometric method for the determination of bo
ron in ceramic materials is described. The method is based on spectrop
hotometric measurement of the decrease in the pH produced by the react
ion between boric acid and mannitol in the presence of an acid-base in
dicator. A bichannel FI (flow injection) manifold in which the sample
solutions were injected into deionized water (at pH 5.4) and the strea
m was later merged with the reagent stream (a mannitol solution contai
ning 1 x 10(-4) mol l(-1) bromocresol green at pH 5.4), was used. Tran
sient signals were monitored at 616 nm. A theoretical model which desc
ribes the dependence between the absorbance values and boric acid conc
entration is presented. The model predicts a non linear dependence bet
ween the absorbance or increment in absorbance and the boric acid conc
entration. In contrast, the model predicts a linear dependence between
the inverse of the absorbance values and the boric acid concentration
. The calibration graphs (1/A vs mu g ml(-1) B2O3) were linear over th
e range 1-30 mu g ml(-1) of B2O3. The relative standard deviations wer
e 0.7 and 0.4% for 4 and 8 mu g ml(-1) of B2O3, respectively. The limi
t of detection was 0.02 mu g ml(-1) of B2O3 (3 sigma criterium). The m
ethod was used to determine boron in nine ceramic materials with very
different nominal boron compositions. The results were compared with t
hose obtained using a potentiometric titration method as reference met
hod. No significant differences (at 95% probability level) were found
between the proposed and reference methods. The method is rapid, relia
ble, precise and free of interferences. (C) 1998 Elsevier Science B.V.