4.7 Article

Catalytic effect of lithium titanate oxide doped with praseodymium on thermal decomposition of ammonium nitrate

Journal

JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY
Volume 147, Issue 1, Pages 263-273

Publisher

SPRINGER
DOI: 10.1007/s10973-020-10243-7

Keywords

Ammonium nitrate; Lithium titanate oxide; Kinetics; Activation energy

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In this study, lithium titanate oxide and praseodymium-doped lithium titanate oxide were synthesized using a sol-gel method, and their catalytic effects on the thermal decomposition of ammonium nitrate were investigated. The results showed that praseodymium doping improved the catalytic activity of lithium titanate oxide.
In this work, lithium titanate oxide (Li4Ti5O12) (LTO) and praseodymium ion doped in lithium titanate oxide (Pr-LTO) were synthesized in a sol-gel simple method, and their catalytic effects on thermal decomposition of ammonium nitrate were reported using thermogravimetric analysis-differential scanning calorimetry (TGA-DSC) techniques. The X-ray powder diffraction, Brunauer-Emmett-Teller surface area measurements, particle size analysis, energy-dispersive X-ray spectroscopy, and scanning electron microscopy techniques were used to identify the structural properties and morphology of LTO and Pr-doped LTO. By doping the praseodymium ion within the LTO spinel structure, the surface area increases (from 204.2 m(2) g(-1) for LTO semiconductor to 318.9 m(2) g(-1) for Pr-doped LTO), and the catalytic activity improved. The catalytic effects of LTO and Pr-LTO on the thermal behavior of AN were studied via TG-DSC techniques. The thermal decomposition of pure AN (196-400 degrees C) shifted to lower temperatures, 154-280 degrees C, and 131-241 degrees C, in the presence of LTO and Pr-LTO, respectively. The results showed that the catalytic effects of LTO were improved by praseodymium doping. The Flynn-Wall-Ozawa (FWO), Kissinger-Akahira-Sunose (KAS), Starink, and Tang methods were used to determine activation energies of all AN samples at different conversion values (alpha). The activation energies of pure AN values were 166 +/- 3, 166 +/- 2, 166 +/- 2, and 162 +/- 2 kJ mol(-1), while AN/LTO activation energies were 145 +/- 2, 144 +/- 1, 144 +/- 1, and 144 +/- 2 kJ mol(-1) and finally, those of AN/Pr-LTO were 112 +/- 1, 109 +/- 2, 110 +/- 1, and 110 +/- 1 kJ mol(-1) using FWO, KAS, Starink, and Tang methods, respectively.

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