T. Sugimoto et al., FORMATION MECHANISM OF UNIFORM CDS PARTICLES FROM CONDENSED CD(OH)(2)SUSPENSION, Journal of colloid and interface science, 176(2), 1995, pp. 442-453
The formation mechanism of uniform cadmium sulfide particles obtained
in large quantities from condensed Cd(OH)(2) suspension in the presenc
e of thioacetamide (TAA), gelatin and NH3-NH4+ buffer system was inves
tigated. Basically, the reaction proceeded through rapid dissolution o
f Cd(OH)(2) particles induced by the reaction of Cd2+ ions with S2- io
ns liberated from TAA in the solution phase. It was finished in ca. 1
min under the standard conditions, 0.5 mol dm(-3) in Cd(OH)(2), 0.55 m
ol dm(-3) in TAA, 1 wt% in deionized gelatin, and 1.0 mol dm(-3) NH4NO
3 at 20 degrees C and at pH 8.50 adjusted with NH3. The resulting unif
orm and nearly spherical particles of CdS prepared under the standard
conditions were 40 nm in mean diameter and were polycrystalline partic
les consisting of randomly oriented much smaller subcrystals (8.60 nm)
. Besides using the NH3-NH4+ system in generating uniform CdS particle
s, employing borax/NaOH buffer system in the formation of spherical Cd
S particles was also possible. It was also found that S2- ions were fu
rnished through a reaction, CH3CSNH2 --> CH3CN + 2H(+) + S2-. This rea
ction was excessively accelerated by the rapid consumption of S2- ions
so that it is thought to be a reversible reaction. The reaction was v
irtually stoichiometric and the contribution of hydrolysis of TAA was
not observed. The uniform growth of the CdS particles was achieved by
the controlled dissolution of the Cd(OH)(2) without aggregation of the
growing CdS particles after an instantaneous nucleation. (C) 1995 Aca
demic Press, Inc.