INFLUENCE OF CRYSTALLIZATION TEMPERATURE ON THE ABSORPTION OF DIBUTYL PHTHALATE IN ZEOLITE A

Authors

  • Ljubica Vasiljević University of East Sarajevo, Faculty of Technology, Karakaj bb, 75400 Zvornik, Republic of Srpska
  • Branko Škundrić Academy of Science and Art of Republic of Srpska, Bana Lazarevića 1, 78000 Banja Luka, Republic of Srpska
  • Dragica Lazić University of East Sarajevo, Faculty of Technology, Karakaj bb, 75400 Zvornik, Republic of Srpska
  • Miladin Gligorić University of East Sarajevo, Faculty of Technology, Karakaj bb, 75400 Zvornik, Republic of Srpska
  • Vladan Mićić University of East Sarajevo, Faculty of Technology, Karakaj bb, 75400 Zvornik, Republic of Srpska

DOI:

https://doi.org/10.7251/COMEN1402197V

Abstract

In order to determine the effect of crystallization temperature on the absorption and properties of zeolite A particles, we have monitored the modified dibutyl phthalate absorption ( DBP ), a degree of crystalline phase, specific surface area, mean diameter of particle ( DS50 % ), and performed scanning electron microscopy ( SEM ) of the synthesized samples of zeolites. The synthesis of samples was carried out at crystallization temperatures of 70, 75, 80, 85 and 90°C ; the raw materials (sodium aluminate and sodium silicate) were heated at 90°C. The particle size of the synthesized samples is similar in most studied systems at all temperatures of crystallization, which is in accordance with the principles of the autocatalytic nucleation and „memory effect” of the gel. An increase in the specific surface area of the synthesized samples with the increase in the crystallization temperature was observed in all the analyzed systems (3.25 to 35.31 m2/g). It was found that the increase of crystallization temperature increases the absorption of dibutyl phthalate(0.90-1.20  cm3/g ); however, at the same time, the proportion of zeolite A in the same samples is reduced, as confirmed by SEM analysis.

References

[1] D. W. Breck, Zeolite Molecular Sieves, Structure, Chemistry and Use, John Wiley&Sons New York, USA 1974.

[2] W. M. Meier, D. H. Olson, Atlas of Zeolite Structure Types, 2nd rev. Edn., Butterworths, London 1987, 127−137.

[3] Z. Yang, Y. S. Lin, Sol-Gel Synthesis of Silicates/γ-Alumina Granules, Ind. Eng. Chem. Res., Vol. 39 (2000) 4944−4948.

[4] Lj. Tanacković, Influence of crystallization conditions on the structure of detergent zeolite [In Serbian: Uticaj uslova kristalizacije na strukturu deterdžentskog zeolita] Master thesis, University of Banja Luka, Faculty of Technology, Banja Luka 2004.

[5] M. J. Eapen, K. S. N. Reddy, V. P. Shiralkar, Hydrothermal crystallization of zeolite beta using tetraethylammonium bromide, Zeolites, Vol. 14−4 (1994) 295−302.

[6] S. Bosnar, B. Subotić, Mechanism and kinetics of the growth of zeolite microcrystals: Part 1: Influence of the alkalinity of the system on the growth kinetics of zeolite A microcrystals, Microporous and mesoporous materials, Vol. 28−3 (1999) 483−493.

[7] T. Antonić, B. Subotić, N. Stubičar, Influence of gel properties on the crystallization of zeolites: Part 1: Influence of alkalinity during gel preparation on the kinetics of nucleation of zeolite A, Zeolites, Vol. 18−4 (1997) 291−300.

[8] J. Bauer, et al., Zeolite/aluminum composite adsorbents for application in adsorption refrige-ration, International Journal of Energy Research, Vol. 33−13 (2009) 1233−1249.

[9] X. Y. Liu, et al., Effects of the Different Crystallization Time on Synthesis of Zeolite 4A from by-Products of Polysilicon Production Process, Advanced Materials Research, Vol. 347 (2012) 246−251.

[10] S. Hui, B. Shen, Effects of organic additives on crystallization process and the adsorption performances of zeolite A, Adsorption, Vol. 18−2 (2012) 103−111.

[11] I. Wilaiporn, K. Rangsriwatananon, Morphology-Controlled Synthesis of Zeolite and Physicochemical Properties, Engineering Journal, Vol. 16−3 (2012) 1−12.

[12] L. Xing-dong, W. Yi-pin, C. Xue-min, H. Yan, M. Jinet, Influence of synthesis parameters on NaA zeolite crystals, Powder Technology, Vol. 243 (2013) 184−193.

Downloads

Published

2014-12-15