Effect of citrate to nitrate ratio on the sol-gel synthesis of nanosized α-Al2O3 powder

2017 ◽  
Vol 43 (17) ◽  
pp. 15221-15226 ◽  
Author(s):  
Pallavi Suhasinee Behera ◽  
Sunipa Bhattacharyya ◽  
Ritwik Sarkar
Materials ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 854
Author(s):  
Antonia Hoppe ◽  
Cornelius Dirksen ◽  
Karl Skadell ◽  
Michael Stelter ◽  
Matthias Schulz ◽  
...  

A new preparation concept of a partially porous solid-state bilayer electrolyte (BE) for high-temperature sodium-ion batteries has been developed. The porous layer provides mechanical strength and is infiltrated with liquid and highly conductive NaAlCl4 salt, while the dense layer prevents short circuits. Both layers consist, at least partially, of Na-β-alumina. The BEs are synthesized by a three-step procedure, including a sol-gel synthesis, the preparation of porous, calcined bulk material, and spin coating to deposit a dense layer. A detailed study is carried out to investigate the effect of polyethylene oxide (PEO) concentration on pore size and crystallization of the bulk material. The microstructure and crystallographic composition are verified for all steps via mercury intrusion, X-ray diffraction, and scanning electron microscopy. The porous bulk material exhibits an unprecedented open porosity for a NaxAlOy bilayer-system of ≤57% with a pore size of ≈200–300 nm and pore volume of ≤0.3 cm3∙g−1. It contains high shares of crystalline α-Al2O3 and Na-β-alumina. The BEs are characterized by impedance spectroscopy, which proved an increase of ionic conductivity with increasing porosity and increasing Na-β-alumina phase content in the bulk material. Ion conductivity of up to 0.10 S∙cm−1 at 300 °C is achieved.


2006 ◽  
Vol 32 (5) ◽  
pp. 587-591 ◽  
Author(s):  
Jiang Li ◽  
Yubai Pan ◽  
Changshu Xiang ◽  
Qiming Ge ◽  
Jingkun Guo

RSC Advances ◽  
2014 ◽  
Vol 4 (57) ◽  
pp. 30081-30089 ◽  
Author(s):  
Anita Raj Sanwaria ◽  
Meena Nagar ◽  
Rakesh Bohra ◽  
Archana Chaudhary ◽  
Shaikh M. Mobin ◽  
...  

Synthesis and characterization of salicylaldehyde-modified aluminum(III) isopropoxide, [(OPri)3−nAl(OC6H4CHO)n] precursors used for sol–gel synthesis of α-Al2O3 nano-rods.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Simon Carstens ◽  
Christian Splith ◽  
Dirk Enke

AbstractOne of the major routes to synthesize macroporous α-Al2O3 is the sol-gel process in presence of templates. Templates include polymers as well as carboxylic acids, such as citric acid. By careful choice of the template, pore diameters can be adjusted between 110 nm and several µm. We report the successful establishment of plain short-chain dicarboxylic acids (DCA) as porogenes in the sol-gel synthesis of macroporous α-Al2O3. By this extension of the recently developed synthesis route, a very precise control of pore diameters is achieved, in addition to enhanced macropore volumes in α-Al2O3. The formation mechanism thereof is closely related to the one postulated for citric acid, as thermal analyses show. However, since branching in the DCA-linked alumina nuclei is not possible, close monomodal pore width distributions are attained, which are accompanied by enhanced pore volumes. This is a significant improvement in terms of controlled enhanced porosity in the synthesis of macroporous α-Al2O3.


Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1787
Author(s):  
Simon Carstens ◽  
Ralf Meyer ◽  
Dirk Enke

This article combines a systematic literature review on the fabrication of macroporous α-Al2O3 with increased specific surface area with recent results from our group. Publications claiming the fabrication of α-Al2O3 with high specific surface areas (HSSA) are comprehensively assessed and critically reviewed. An account of all major routes towards HSSA α-Al2O3 is given, including hydrothermal methods, pore protection approaches, dopants, anodically oxidized alumina membranes, and sol-gel syntheses. Furthermore, limitations of these routes are disclosed, as thermodynamic calculations suggest that γ-Al2O3 may be the more stable alumina modification for ABET > 175 m2/g. In fact, the highest specific surface area unobjectionably reported to date for α-Al2O3 amounts to 16–24 m2/g and was attained via a sol-gel process. In a second part, we report on some of our own results, including a novel sol-gel synthesis, designated as mutual cross-hydrolysis. Besides, the Mn-assisted α-transition appears to be a promising approach for some alumina materials, whereas pore protection by carbon filling kinetically inhibits the formation of α-Al2O3 seeds. These experimental results are substantiated by attempts to theoretically calculate and predict the specific surface areas of both porous materials and nanopowders.


2019 ◽  
Vol 207 ◽  
pp. 301-309 ◽  
Author(s):  
Xiuying Tian ◽  
Shixun Lian ◽  
Jin Wen ◽  
Changyan Ji ◽  
Zhanjun Chen ◽  
...  
Keyword(s):  
Sol Gel ◽  
Α Al2o3 ◽  

2006 ◽  
Vol 314 ◽  
pp. 201-206 ◽  
Author(s):  
Tanja Damjanović ◽  
Christos Argirusis ◽  
B. Jokanović ◽  
Günter Borchardt ◽  
Kirsten Moritz ◽  
...  

Combining sol-gel synthesis of 3/2 mullite through hydrolysis and condensation of tetraethoxysilane and aluminum-tri-sec-butylate with electrophoretic deposition (EPD) yields sufficiently thick and homogeneous layers which transform into mullite at T ≥ 1000 °C. The characterisation of the mullite precursor during synthesis was performed through electroacustic measurements. The protectiveness of the deposited mullite layers was tested in air in the temperature range 1200 °C ≤ T ≤ 1550 °C by means of isothermal thermogravimetric analysis for up to 200 hours. Comparing the oxidation rate of mullite coated C/C-Si-SiC samples to that of uncoated reference samples clearly demonstrated that mullite offers a significant improvement to the oxidation resistance of the uncoated material. At temperatures above 1600 °C the protectiveness of the deposited layer is reduced due to the existence of a liquid phase and the formation of CO bubbles above the cracks in the SiC layer. In order to prolong the protectiveness of our mullite layers at higher temperatures we deposited an additional layer from a suspension of mullite precursor with 5 wt. % of Al2O3 powder. The protectiveness of so obtained mullite and mullite/ Al2O3 layers was also tested under cyclic conditions at 1500 °C and 1550 °C. These experiments clearly demonstrated that all samples withstood at least for 4-10 cycles which were performed subsequently in different time intervals (from 2-3 days to 1 h).


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