Facile preparation of CaCO3 nanoparticles with self-dispersing properties in the presence of dodecyl dimethyl betaine

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Abstract

CaCO3 nanoparticles with about 50 nm in size could be prepared by carbonation reaction of a mixture of Ca(OH)2 and dodecyl dimethyl betaine (BS-12) via bubbling CO2 gas. The samples were characterized by transmission electron microscopy (TEM), photon correlation spectroscopy (PCS) and photograph. The results indicate that the CaCO3 powder samples can self-diffuse in water, thus forming a suspension with enhanced stability and longevity. Fourier transform infrared spectroscopy (FT-IR) of the CaCO3 particles showed the appearance of the alkyl groups from BS-12. The CaCO3 nucleated in the presence of BS-12 exhibited different endothermic peak compared to one nucleated in the absence of BS-12 in thermal gravimetric analysis (TGA). We have succeeded in surface modification of CaCO3 with BS-12. The presence of BS-12 accelerates the period of absorption and shortens the time of carbonation.

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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