Abstract
The ion exchange properties of hydrous titania gels of different particle sizes, precipitated from titanous chloride through the agency of ammonium carbonate and hydroxide have been studied. Such studies were carried out under acidic and alkaline conditions with respect to Cu2+, Ni2+, Co2+ and Cr3+ ions.
In the case of gels precipitated by ammonium carbonate, oxygen gas was used as the oxidizing agent whereas with ammonium hydroxide as precipitant, oxidation was performed with hydrogen peroxide.
Ion exchange capacities were determined by visible spectrophotometry. Increasing the pH of preparation lead to an increase in exchange capacities of the hydroxide precipitated gels that are characterized to be mesoporous. Such an increase is not observed in the case of carbonate precipitated microporous gels. It is shown that in the latter case the NH +4 ions generated by the initial interaction of (NH4)2CO3 with the acidic titanous chloride lead to the formation of titania exchangers that are predominantly in the ammonium form. The textural characteristics of the exchanger resulting from different conditions of preparation is a significant contributing parameter to the resulting data.
Ageing of the microporous titania samples markedly reduces the exchanger capacity of the smaller Ni2+ ions but increases that of the bulkier Cr3+ as a result of the presence of some wide pores that appear upon agglomeration. The presence of Cr3+ ions in the hydroxo form in solution seems to inhibit its exchange with the appropriate surface species.
Studies on the kinetics of exchange with respect to the Ni2+ ions seem to indicate that a particle diffusion mechanism is partly or completely responsible for the rate of exchange.
Similar content being viewed by others
References
G. E. Boyd and B. A. Soldano, J. Amer. Chem. Soc. 75 (1953) 6091.
J. P. Bonsack, J. Colloid Interface Sci. 44 (1973) 430.
Y. Inove and M. Tauji, J. Nucl. Sci. Technol. 13 (1976) 85.
A. M. Andrianov, V. P. Koryukova, V. E. Roladyan, L. K. Sakhno, L. V. Smirnova and E. V. Shabanov, Zh. Prikl. Khim. 51 (1978) 1892.
T. Sazaki, Y. Komatsu and Y. Fujiki, Sep. Sci. Technol. 18 (1983) 49.
M. Tsuji, M. Abe and M. Orimo, Bull. Chem. Soc. Jpn 58 (1985) 97.
Y. Komatsu, Y. Fujiki and T. Sasaki, ibid. 59 (1986) 49.
J. Ragai and S. I. Selim, J. Colloid Interface Sci. 115 (1986) 139.
T. D. Semenouskaya, M. Deak and K. V. Chamutov, Zh. Fiz. Khim. 49 (1975) 462.
M. Abe, M. Tsuji, S. P. Qureshi and H. Uchikoshi, Chromatographia 13 (1980) 626.
H. Kita, N. Henmi, K. Shimazu and K. Tanabe, J. C. S., Faraday Trans. I. 77 (1981) 2451.
H. P. Boehm, Adv. Catal. 16 (1966) 179.
J. Ragai, J. Chem. Tech. Biotechnol. 44 (1989) 237.
J. Ragai, K. S. W. Sing, R. Mikhail, ibid. 30 (1980) 1.
K. Nakamoto, in “Infrared and Raman Spectra of Inorganic and Coordination Compounds” (John Wiley, New York, 1978) pp. 288.
J. Ragai, Nature 325 (1987) 703.
M. L. Hair, J. Phys. Chem. 74 (1970) 1290.
M. Elsaidi, MSc, Thesis, American University in Cairo, Egypt (1989).
C. F. Boes Jr and R. E. Meswar, (eds) “The Hydrolysis of Cations” (John Wiley, New York, 1976) pp. 218.
J. Ragai and K. S. W. Sing, J. Colloid Interface Sci. 101 (1984) 369.
J. E. Huheey, “Inorganic Chemistry Principals of Structure and Reactivity” (Harper and Row, New York, 1983).
V. V. Strelko, S. A. Khainakov, A. P. Kuasheuko, V. N. Belyakov and A. I. Bortun, Zh. Prikl. Khim (Leningrad) 61 (1988) 2124.
S. A. Selim and H. A. Hassan, Thermochimica Acta 45 (1981) 349.
N. N. Greenwood and A. Earnshaw, “Chemistry of the Elements” (Pergamon Press, Oxford, 1984).
Y. Inove and M. Yamazaki, Bull. Chem. Soc. Jpn 53 (1980) 811.
G. E. Boyd, A. W. Adamson and L. S. Myers, J. Amer. Chem. Soc. 69 (1947) 2836.
D. Reichenberg, ibid. 75 (1953) 589.
S. T. Gregg and K. S. W. Sing, “Adsorption, Surface Area and Porosity” (Academic, London, 1967) pp. 201.
G. H. Nancollus and R. Paterson, J. Inorg. Nucl. Chem. 22 (1961) 259.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Yacoub, N., Ragai, J. & Selim, S.A. Hydrous oxides of titanium: cation exchange properties and kinetics of exchange. J Mater Sci 26, 4937–4944 (1991). https://doi.org/10.1007/BF00549874
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF00549874