中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Transformation of Gibbsite to Boehmite in Caustic Aqueous Solution at Hydrothermal Conditions

文献类型:期刊论文

作者Zhang, Xin2; Cui, Wenwen1,2,5; Hu, Jian Zhi2; Wang, Hsiu-Wen3; Prange, Micah P.2; Wan, Chuan2; Jaegers, Nicholas R.2; Zong, Meirong2,4; Zhang, Hailin1,2,5; Pearce, Carolyn, I2
刊名CRYSTAL GROWTH & DESIGN
出版日期2019-10-01
卷号19期号:10页码:5557-5567
ISSN号1528-7483
DOI10.1021/acs.cgd.9b00468
英文摘要Phase transformations among aluminum (oxyhydr)oxide minerals play important roles across a wide range of natural and industrial settings. In highly caustic aqueous solutions, uncertainty persists regarding whether solid-state or dissolution-reprecipitation pathways dominate. We explored the transformation of gibbsite [alpha-Al(OH)(3)] to boehmite (gamma-AlOOH) in caustic NaOH solution at hydrothermal conditions as a function of temperature, Al(III) and NaOH concentrations, and reaction time. Comparison of detailed structural and morphological solids characterization by X-ray diffraction, scanning electron microscopy/transmission electron microscopy, atomic force microscopy, Raman spectroscopy, and high-field Al-27 MAS NMR to predictions from equilibrium thermodynamics calculations suggests the critical importance of dissolution-reprecipitation across our range of system conditions. The yield and physical properties of the boehmite product were found to be sensitive to the hydrothermal treatment temperature and the Al/OH- ratio, controlled by the loading of gibbsite with respect to NaOH. Experiments at lower Al/OH- ratios (e.g., 0.64) indicate that the dissolution of the gibbsite reaches an aqueous aluminate saturation state sufficient to overcome the nucleation barrier for boehmite. Higher Al/OH- ratios (e.g., 3.2) are found to slow the phase transformation, leaving residual unreacted gibbsite in the final product. Higher temperatures appear to improve the phase transformation rate but also typically yield smaller-sized boehmite particles. Particle morphological analyses compared to thermodynamic expectations suggest an important role of kinetics at mineral/solution interfaces, both in the gibbsite dissolution rate as well as the growth rate of boehmite nanocrystals.
WOS关键词HIGH-TEMPERATURE SOLUBILITY ; IONIC-STRENGTH ; ALUMINATE SOLUTIONS ; GAMMA-ALUMINA ; GROWTH ; PRECIPITATION ; TRANSITIONS ; PARTICLES ; STABILITY ; BAYERITE
资助项目IDREAM (Interfacial Dynamics in Radiation Environments and Materials), an Energy Frontier Research Center - U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences (BES) ; DOE Office of Biological and Environmental Research ; DOE[DE-AC05-76RL01830]
WOS研究方向Chemistry ; Crystallography ; Materials Science
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000489001700016
资助机构IDREAM (Interfacial Dynamics in Radiation Environments and Materials), an Energy Frontier Research Center - U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences (BES) ; DOE Office of Biological and Environmental Research ; DOE
源URL[http://ir.ipe.ac.cn/handle/122111/31117]  
专题中国科学院过程工程研究所
通讯作者Zhang, Xin; Rosso, Kevin M.
作者单位1.Univ Chinese Acad Sci, Beijing, Peoples R China
2.Pacific Northwest Natl Lab, Richland, WA 99352 USA
3.Oak Ridge Natl Lab, Oak Ridge, TN 37830 USA
4.Nanjing Univ, Sch Earth Sci & Engn, Nanjing, Jiangsu, Peoples R China
5.Chinese Acad Sci, Inst Proc Engn, Beijing, Peoples R China
6.Washington State Univ, Dept Chem, Pullman, WA 99164 USA
推荐引用方式
GB/T 7714
Zhang, Xin,Cui, Wenwen,Hu, Jian Zhi,et al. Transformation of Gibbsite to Boehmite in Caustic Aqueous Solution at Hydrothermal Conditions[J]. CRYSTAL GROWTH & DESIGN,2019,19(10):5557-5567.
APA Zhang, Xin.,Cui, Wenwen.,Hu, Jian Zhi.,Wang, Hsiu-Wen.,Prange, Micah P..,...&Rosso, Kevin M..(2019).Transformation of Gibbsite to Boehmite in Caustic Aqueous Solution at Hydrothermal Conditions.CRYSTAL GROWTH & DESIGN,19(10),5557-5567.
MLA Zhang, Xin,et al."Transformation of Gibbsite to Boehmite in Caustic Aqueous Solution at Hydrothermal Conditions".CRYSTAL GROWTH & DESIGN 19.10(2019):5557-5567.

入库方式: OAI收割

来源:过程工程研究所

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