Ductile Phase Toughened Ceramics by Partial Reduction Reactions in the Ni-AI-O System: Mechanical Properties and Effect of Dopants

1994 ◽  
Vol 365 ◽  
Author(s):  
E. Üstündağ ◽  
P. Ret ◽  
Y. Shapiro ◽  
R. Subramanian ◽  
R. Dieckmann ◽  
...  

ABSTRACTPartial reduction reactions in the Ni-Al-O system, starting with the spinel compound NiAl2O4, are used to form metal-ceramic microstructures in situ. Two different morphologies of nearly pure Ni particles, equiaxed and rod-like, form within a ceramic matrix depending on the choice of processing parameters. Electron microscopy studies were performed for microstructural characterization, phase identification and chemical analysis. The fracture toughness of the Ni-Al2O3 mixture was significantly improved with respect to that of the original spinel phase. It is shown that cracking at the original spinel grain boundaries, likely due to the large volume changes associated with the reduction reaction, can be avoided by the addition of small amounts of ZrO2. It is seen that ZrO2 also acts as a nucleation site for the precipitating metal and hence allows morphology control in microstructures obtained by partial reduction reactions.

RSC Advances ◽  
2019 ◽  
Vol 9 (18) ◽  
pp. 10314-10319 ◽  
Author(s):  
Yazhou Qin ◽  
Yuxiang Lu ◽  
Wufan Pan ◽  
Dongdong Yu ◽  
Jianguang Zhou

We prepared hollow flower-shaped Au nanoparticles as a bifunctional material by a one-pot method for in situ monitoring of reduction reactions.


1995 ◽  
Vol 398 ◽  
Author(s):  
Z. Zhang ◽  
E. Üstündag ◽  
S.L. Sass

ABSTRACTMetal-ceramic microstructures were formed in situ by partial reduction of the spinel compound NiAl2O4. At 1300°C the reduction reaction passed through an intermediate stage involving the formation of Ni and metastable “defect spinel” phases, before the appearance of the equilibrium phases, Ni + α-Al2O3. At 1100°C, depending on the reduction time, the products of the reduction reaction were Ni and the metastable “defect spinel” for less than 24 hours; Ni + θ-Αl2Ο3 for 24-48 hours; and Ni + GI-AI2O3 for 144-168 hours. The effects of dopants, such as Cr2O3, MgO, TiO2 and Y2O3, on the reduction mechanism and kinetics were examined and shown, in the case of TiO2, to have a controlling influence. A reduction reaction mechanism is proposed.


1994 ◽  
Vol 365 ◽  
Author(s):  
R. Subramanian ◽  
E. Üstündağ ◽  
S.L. Sass ◽  
R. Dieckmann

ABSTRACTThe influence of the addition of impurities and changes in the oxygen partial pressure on the formation of metal-ceramic microstructures by partial reduction of ternary or higher ceramic oxides was experimentally investigated in the model system Fe-Mn-C at constant temperature and total pressure. Electron microscopy studies were performed for microstructural characterization, phase identification and chemical analysis. It was observed that the addition of dopants such as BaO, CaO, MgO, SrO, Al2O3, Cr2 O3 or ZrO2 to the initial, polycrystalline oxide solid solution (Fel−xMnx)1−ΔO strongly influences the location and rate of metal precipitation during reduction. Experimental observations are discussed based on solubility limits and the segregation of dopants.


1995 ◽  
Vol 75 ◽  
pp. 241-255 ◽  
Author(s):  
R. Subramanian ◽  
E. Üstündagˇ ◽  
S.L. Sass ◽  
R. Dieckmann

2011 ◽  
Vol 409 ◽  
pp. 215-220 ◽  
Author(s):  
Mohammed Shamekh ◽  
Martin Pugh ◽  
Mamoun Medraj

TiC and TiB2compounds in the form of interpenetrating network reinforced AZ91D magnesium matrix composites have been successfully synthesized by anin-situreactive infiltration technique. In this process, the ceramic reinforcement phases, TiC and TiB2, were synthesizedin-situfrom elemental powders of Ti and B4C without any addition of a third metal powder such as Al. The molten Mg alloy infiltrates the preform of Tipand B4Cpby the capillary force. The microstructure and reaction mechanism are investigated using SEM/EDS and XRD analysis. The results show that the processing parameters such as temperature, holding time and the green compact relative density have a significant influence on the reaction mechanism and the fabrication of the composite. In addition, the infiltrated Mg acts as an intermediary that makes the reaction possible at a lower temperature than that required for solid-state reaction between Ti and B4C. Microstructural characterization reveals a relatively uniform distribution of the reinforcing phases, TiC and TiB2in the Mg matrix.


1995 ◽  
Vol 195 ◽  
pp. 39-50 ◽  
Author(s):  
E. Üstünda ◽  
P. Ret ◽  
R. Subramanian ◽  
R. Dieckmann ◽  
S.L. Sass

2017 ◽  
Vol 120 (3) ◽  
pp. 303-322
Author(s):  
D. Pienaar ◽  
B.M. Guy ◽  
C. Pienaar ◽  
K.S. Viljoen

Abstract Mineralogical and textural variability of ores from different sources commonly leads to processing inefficiencies, particularly when a processing plant is designed to treat ore from a single source (i.e. ore of a relatively uniform composition). The bulk of the Witwatersrand ore in the Klerksdorp goldfield, processed at the AngloGold Ashanti Great Noligwa treatment plant, is derived from the Vaal Reef (>90%), with a comparatively small contribution obtained from the Crystalkop Reef (or C-Reef). Despite the uneven contribution, it is of critical importance to ensure that the processing parameters are optimized for the treatment of both the Vaal and C-Reefs. This paper serves to document the results of a geometallurgical study of the C-Reef at the Great Noligwa gold mine in the Klerksdorp goldfield of South Africa, with the primary aim of assessing the suitability of the processing parameters that are in use at the Great Noligwa plant. The paper also draws comparisons between the C-Reef and the Vaal Reef A-facies (Vaal Reef) and attempts to explain minor differences in the recovery of gold and uranium from these two sources. Three samples of the C-Reef were collected in-situ from the underground operations at Great Noligwa mine for mineralogical analyses and metallurgical tests. Laboratory-scale leach tests for gold (cyanide) and uranium (sulphuric acid) were carried out using dissolution conditions similar to that in use at the Great Noligwa plant, followed by further diagnostic leaching in the case of gold. The gold in the ore was found to be readily leachable with recoveries ranging from 95% to 97% (as opposed to 89% to 93% for the Vaal Reef). Additional recoveries were achieved in the presence of excess cyanide (96% to 98%). The recovery of uranium varied between 72% and 76% (as opposed to 30% to 64% for the Vaal Reef), which is substantially higher than predicted, given the amount of brannerite in the ore, which is generally regarded as refractory. Thus, the higher uranium recoveries from the C-Reef imply that a proportion of the uranium was recovered by the partial dissolution of brannerite. As the Vaal Reef contain high amounts of chlorite (3% to 8%), which is an important acid consumer, it is considered likely that this could have reduced the effectiveness of the H2SO4 leach in the case of the ore of the Vaal Reef. Since the gold and uranium recoveries from the C-Reef were higher than the recoveries from the Vaal Reef, the results demonstrate that the processing parameters used for treatment of the Vaal Reef are equally suited to the treatment of the C-Reef. Moreover, small processing modifications, such as increased milling and leach retention times, may well increase the recovery of gold (particularly when e.g. coarse gold, or unexposed gold, is present).


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Luqman Ali Shah ◽  
Rida Javed ◽  
Mohammad Siddiq ◽  
Iram BiBi ◽  
Ishrat Jamil ◽  
...  

AbstractThe in-situ stabilization of Ag nanoparticles is carried out by the use of reducing agent and synthesized three different types of hydrogen (anionic, cationic, and neutral) template. The morphology, constitution and thermal stability of the synthesized pure and Ag-entrapped hybrid hydrogels were efficiently confirmed using scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and thermo gravimetric analysis (TGA). The prepared hybrid hydrogels were used in the decolorization of methylene blue (MB) and azo dyes congo red (CR), methyl Orange (MO), and reduction of 4-nitrophenol (4-NP) and nitrobenzene (NB) by an electron donor NaBH4. The kinetics of the reduction reaction was also assessed to determine the activation parameters. The hybrid hydrogen catalysts were recovered by filtration and used continuously up to six times with 98% conversion of pollutants without substantial loss in catalytic activity. It was observed that these types of hydrogel systems can be used for the conversion of pollutants from waste water into useful products.


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