Analysis of Mechanically Induced Reactivity of Boehmite Using Kinetics of Boehmite to γ-Al2O3 Transformation

被引:22
作者
Alex, T. C. [1 ]
Kumar, C. Sasi [2 ]
Kailath, Ansu J. [1 ]
Kumar, Rakesh [1 ]
Roy, S. K. [3 ]
Mehrotra, S. P. [4 ]
机构
[1] Natl Met Lab, Jamshedpur 831007, Bihar, India
[2] Maulana Azad Natl Inst Technol, Dept Mat Sci & Met Engn, Bhopal 462051, India
[3] Indian Inst Technol, Dept Met & Mat Engn, Kharagpur 721302, W Bengal, India
[4] Indian Inst Technol, Dept Mat Sci & Engn, Kanpur 208016, Uttar Pradesh, India
来源
METALLURGICAL AND MATERIALS TRANSACTIONS B-PROCESS METALLURGY AND MATERIALS PROCESSING SCIENCE | 2011年 / 42卷 / 03期
关键词
THERMAL-DECOMPOSITION; GAMMA-ALOOH; ALUMINA; DEHYDRATION; TEMPERATURE; GIBBSITE; SIZE;
D O I
10.1007/s11663-011-9494-5
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
This article focuses on the mechanically induced reactivity of boehmite prepared by thermal decomposition of gibbsite. Boehmite, which retained the morphology of gibbsite, was characterized by a specific surface area of 264 m(2)/g. Mechanical activation (MA) was carried out in a planetary mill up to 240 minutes. The samples were characterized in terms of morphology, characteristic particle diameters, Brunauer Emmett Teller (BET) specific surface area (SSA(BET)), microcrystallite dimension (MCD), microstrain (epsilon) and Fourier transform infrared spectroscopy. The reactivity was construed from the kinetics of thermal transformation of boehmite into gamma-Al2O3. The transformation observed between 600 K and 900 K (327 A degrees C and 627 A degrees C), manifested itself as two overlapping peaks in the differential thermogravimetric plot. These peaks correspond to two stages of dehydroxylation involving Al2OH and AlOH groups in succession. The peaks were resolved using Gaussian deconvolution. The reactivity was assessed separately for the two stages by comparing the fraction reacted in MA samples (alpha) with that of nonactivated sample (alpha (ref)). During both stages, enhanced kinetics, as revealed by alpha-alpha (ref) plots, indicated an increase in reactivity with MA. The transformation mechanism conformed to n (th) order reaction (f[alpha] = [1 - alpha] (n) with n = 1.3-1.5 in both stages). Values of n remained similar for the activated and reference samples. Activation energies (E (a)) for the first and second dehydroxylation stages were respectively 115 and 300 kJ/mol for the nonactivated sample. E (a) for the second stage decreased exponentially to a value of 222 kJ/mol after 240 minutes of milling. An anomalous negative correlation between reactivity and SSA(BET) was observed. Reactivity parameters were strongly correlated with MCD and epsilon. A plausible explanation for the observed correlations is presented.
引用
收藏
页码:592 / 603
页数:12
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