Myristic acid as surface modifier of calcium carbonate hydrophobic nanoparticles

被引:0
作者
Laiza Marinho Racca
Luíz Carlos Bertolino
Christine Rabello Nascimento
Ana Maria F. de Sousa
Leila Y. Reznik
Lídia Yokoyama
Ana Lúcia Nazareth da Silva
机构
[1] Instituto de Macromoléculas Professora Eloisa Mano,Universidade Federal do Rio de Janeiro
[2] Centro de Tecnologia Mineral,Programa de Engenharia Metalúrgica (PEMM/COPPE/UFRJ)
[3] Universidade Federal do Rio de Janeir,Instituto de Química
[4] Universidade do Estado do Rio de Janeir,Programa de Pós
[5] Universidade Federal do Rio de Janeiro,Graduação em Engenharia de Processos Químicos e Bioquímicos (EPQB)
[6] Universidade Federal do Rio de Janeiro,Programa de Engenharia Ambiental
来源
Journal of Nanoparticle Research | 2019年 / 21卷
关键词
Calcium carbonate; Nanoparticles; Synthesis; Surface modifiers; Myristic acid; Stearic acid;
D O I
暂无
中图分类号
学科分类号
摘要
Several papers describe the treatment of calcium carbonate (CaCO3) with stearic acid acting as a surface modifier, in order to avoid particle coalescence and, at the same time, enhancing filler hydrophobic properties. However, there is still a lack of data relating the efficiency of a traditional modifier used, stearic acid, in the synthesis of CaCO3 nanofiller with other modifiers in terms of inhibition of the agglomeration process during the synthesis. Thus, the present work evaluates the stability of CaCO3 nanoparticles obtained by a carbonation reaction, considering the contents of the crystallization inhibitor (trisodium phosphate-Na3PO4) and the surface modifier (myristic acid) applied. In order to achieve an efficient carbonation process, a bubbling system was used. The results showed that higher surface modifier and crystallization inhibitor contents lead to a narrower particle size distribution and a lower particle size. Comparing the CaCO3 nanoparticles coated with myristic acid (CaCO3-MA) and with stearic acid (CaCO3-SA), it was observed that CaCO3-MA has a higher thermal stability and a lower particle size in relation to CaCO3-SA. Besides this, a more spherical geometry was achieved for CaCO3-MA nanoparticles due to the bubbling system applied during the carbonation reaction.
引用
收藏
相关论文
共 155 条
  • [1] Andreassen Jens-Petter(2005)Formation mechanism and morphology in precipitation of vaterite—nano-aggregation or crystal growth? Journal of Crystal Growth 274 256-264
  • [2] Bhanvase B.A.(2011)Process intensification of encapsulation of functionalized CaCO3 nanoparticles using ultrasound assisted emulsion polymerization Chemical Engineering and Processing: Process Intensification 50 1160-1168
  • [3] Pinjari D.V.(2016)Chemical surface modification of calcium carbonate particles with stearic acid using different treating methods Applied Surface Science 378 320-329
  • [4] Gogate P.R.(2010)Carbonization synthesis of hydrophobic CaCO3 at room temperature Colloids and Surfaces A: Physicochemical and Engineering Aspects 353 97-103
  • [5] Sonawane S.H.(2013)Ethanol assisted synthesis of pure and stable amorphous calcium carbonate nanoparticles Chemical Communications 49 9564-54
  • [6] Pandit A.B.(2003)Time dependent changes in zeta potential of freshly precipitated calcium carbonate Colloids and Surfaces A: Physicochemical and Engineering Aspects 222 41-214
  • [7] Cao Zhi(2018)The choice of precursors in the synthesizing of CuMnOx catalysts for maximizing CO oxidation International Journal of Industrial Chemistry 9 199-316
  • [8] Daly Michael(2018)Cobalt doped CuMnOx catalysts for the preferential oxidation of carbon monoxide Applied Surface Science 441 303-6660
  • [9] Clémence Lopez(2017)Synthesis of CaCO3 nano- and micro-particles by dry ice carbonation Chemical Communications 53 6657-49
  • [10] Geever Luke M.(2013)Effects of cationic surfactant during the precipitation of calcium carbonate nano-particles on their size, morphology, and other characteristics Colloids and Surfaces A: Physicochemical and Engineering Aspects 422 44-6076