TY - JOUR
T1 - Application of internal standardization to rapid coprecipitation technique using lanthanum phosphate for flame atomic absorption spectrometric determination of iron and lead
AU - Kagaya, Shigehiro
AU - Malek, Zanariah Abdul
AU - Araki, Yasuko
AU - Hasegawa, Kiyoshi
PY - 2002/8
Y1 - 2002/8
N2 - By applying an internal standardization, we could use a rapid coprecipitation technique using lanthanum phosphate as a coprecipitant for preconcentration of iron(III) and lead in their flame atomic absorption spectrometric determination. Indium as an internal standard was added to the initial sample solution together with lanthanum and phosphoric acid; the coprecipitation of iron(III) and lead was then carried out at pH about 3. After measuring the atomic absorbances of iron, lead, and indium in the final sample solution, we determined the contents of iron(III) and lead in the original sample solution by using the internal standardization with indium. In this method, complete collection of the precipitate was not required after the coprecipitation of iron(III), lead, and indium, because the ratio of the recovery of iron(III) or lead to that of indium was almost constant regardless of the recovery of the precipitate. This method was simple and rapid, and was available for the determination of 2 - 300 μg L-1 of iron(III) and 5 - 400 μg L-1 of lead in some water samples.
AB - By applying an internal standardization, we could use a rapid coprecipitation technique using lanthanum phosphate as a coprecipitant for preconcentration of iron(III) and lead in their flame atomic absorption spectrometric determination. Indium as an internal standard was added to the initial sample solution together with lanthanum and phosphoric acid; the coprecipitation of iron(III) and lead was then carried out at pH about 3. After measuring the atomic absorbances of iron, lead, and indium in the final sample solution, we determined the contents of iron(III) and lead in the original sample solution by using the internal standardization with indium. In this method, complete collection of the precipitate was not required after the coprecipitation of iron(III), lead, and indium, because the ratio of the recovery of iron(III) or lead to that of indium was almost constant regardless of the recovery of the precipitate. This method was simple and rapid, and was available for the determination of 2 - 300 μg L-1 of iron(III) and 5 - 400 μg L-1 of lead in some water samples.
UR - http://www.scopus.com/inward/record.url?scp=0036670232&partnerID=8YFLogxK
U2 - 10.2116/analsci.18.923
DO - 10.2116/analsci.18.923
M3 - 学術論文
C2 - 12200841
AN - SCOPUS:0036670232
SN - 0910-6340
VL - 18
SP - 923
EP - 926
JO - Analytical Sciences
JF - Analytical Sciences
IS - 8
ER -