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The surfactant –sensitized analytical reaction of niobium with some thiazolylazo compounds.

• 2000
العودة
معلومات البحث
المؤلفون Alaa S. Amin
الكلمات المفتاحية Not Available
المجلة العلمية Not Available
الناشر Not Available
المجلد Not Available
العدد Not Available
الصفحات Not Available
publication.type Local
رابط البحث Not Available
المواد المرفقة Not Available
الملخص
Cationic surfactants, such as cetylpyridinium bromide (CPB), sensitize the color reaction of Nb(V) with 1-(2-benzothiazolylazo)-2-hydroxy-3-naphthoic acid (Ia), 5-(benzothiazolylazo)2,5-naphthalenediol (Ib), 5-(2-benzothiazolylazo)8-hydroxyquinoline (Ic) and 4-(2- benzothiazolylazo)2,2̄-biphenyldiol (Id) reagents. The formation of a ternary complex of stoichiometric ratio 1:2:2 (Nb-R-CPB) is responsible for the observed enhancement in the molar absorptivity and the Sandell sensitivity of the formed complex, when a surfactant is present. The ternary complex exhibits absorption maxima at 649, 692, 661 and 612 nm, (ε=3.35×104, 3.59×104, 4.46×104 and 2.79×104 l mol−1 cm−1) on using reagent Ia, Ib, Ic, and Id, respectively. Beer’s law is obeyed between 0.05 and 2.50 μg ml−1, while applying the Ringbom method for more accurate results is in the range from 0.20 to 2.30 μg ml−1. Conditional formation constants in the presence and absence of CPB for niobium complexes have been calculated. On the basis of a detailed spectrophotometric study, the nature of the chromophoric reagent–surfactant interaction and the peculiar features of the sensitization by CPB are discussed.