Colloids and Surfaces A: Physicochemical and Engineering Aspects
Facile preparation of CaCO3 nanoparticles with self-dispersing properties in the presence of dodecyl dimethyl betaine
Introduction
CaCO3 is the cheapest commercially available inorganic particles, and has been extensively used in many industrial products such as paints, inks, papers, plasticizers, and so on. However, a key problem remains: can CaCO3 be dispersed stably and homogeneously in media? The development of many novel materials requires smaller sized particles and good dispersing properties in water, to form a stable suspension [1], [2], [3], [4]. Recently, the synthesis of organic–inorganic hybrids by mimicking biomineralization has attracted great attention [5], [6]. It has been known that organic additives introduced to the crystallization processes of CaCO3 modified the shapes of crystals and retarded nucleation and growth rate [7], [8], [9], [10], [11], [12], [13], [14], [15]. However, these are not yet the reports about that the organic additive cannot only control the particle size and shape but also render CaCO3 with self-dispersing property in situ. Synthesis of CaCO3 was followed by two basic synthetic routes: the solution route and the carbonation route. The carbonation method is an industrially useful method and preferred in terms of environment preservation, but it is difficult to control the crystal shape and modification of CaCO3. In the study, we studied the crystallization of CaCO3 in the presence of BS-12 by a carbonation route mimicking the essential functions of biomineralization, and the self-dispersing CaCO3 nanoparticles were obtained in this procedure.
Section snippets
Experimental
All of the chemical reagents used were of analytical grade in this experiment. The procedure employed for the synthesis of CaCO3 was as follows. The 10 g of CaO was digested in 100 ml of 80 °C distilled water to form Ca(OH)2 slurry. After a day, the slurry was filtered through a 200 meshes sieve in order to remove the impurity and large particles and then transferred into a 250 ml three-necked flask. After addition of BS-12 into the flask, the mixture was stirred vigorously for 1 h at room
Results and discussion
From Fig. 1a we could see that the spindle-like CaCO3 with the diameter of about 100 nm (the ratio of diameter to length about 1:4) were obtained in the absence of BS-12. However, in the presence of BS-12, the cubic-like CaCO3 in the average particle size of about 50 nm were synthesized as shown in Fig. 1b. In this reaction, the little cubic-like crystals formed in initial stage. The BS-12 used in this study could accelerate the carbonation and improve the speed of nucleation (see Fig. 7). So the
Conclusion
We have succeeded in surface modification of CaCO3 particles in situ with BS-12 in aqueous solution at room temperature. The BS-12 was used in carbonation process to control the particle size and shape and modify the surface of CaCO3 particles simultaneously. In this study the cubic-like CaCO3 particles in the average size of about 50 nm can be synthesized. A suspension of CaCO3 can be formed by self-dispersing of the powder in water, which has enhanced stability and can be preserved for a long
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