Influence of Thermal Treatment on Phase Transformation and Dissolubility of Aluminosilicate Phase in Red Mud

2012 ◽  
Vol 1488 ◽  
Author(s):  
Nan Ye ◽  
Jing Zhu ◽  
Jianwen Liu ◽  
Yalin Li ◽  
Xinyuan Ke ◽  
...  

ABSTRACTRed mud is a solid waste residue from the caustic soda leaching of bauxite ores to produce alumina by the Bayer process. Red mud contains large quantity of alkali and aluminosilicate, so it is potentially available to prepare inorganic polymeric materials by geopolymerisation process. However, the activity or dissolubility of the aluminosilicate phases in red mud is significantly poor, which constraints the geopolymerisation process. Therefore, some pretreatment process for red mud is necessary to improve the adhesive property and dissolubility of Bayer red mud. In this study, mineral phase transformation and dissolubility of a typical red mud sample were studied under different thermal treatment processes. The thermal behavior of the red mud was studied by TG-DTA. The crystalline phases of the samples calcined at 200-1000 °C for different hours were determined by XRD, and the dissolubility was determined by alkaline leaching test. The TG-DTA pattern shows no obvious endothermic or exothermic peaks, and the weight loss increases continuously as the temperature rises, which indicates that the crystalline phases transform continuously as the temperature rises, consistent with the XRD results. As the calcination temperature rises from 200 to 800 °C, several kinds of crystalline phase in original red mud, including gibbsite, katoite, muscovite, natrodavyne disappeared in succession, accompanied with the formation of nepheline, gehlenite, sodium aluminum silicate, and some amorphous aluminosilicate. The calcined products are more likely to dissolve. But when it rises over than 800 °C, the content of gehlenite increases, and the phase of which is stable. As the calcination temperature rises from 200 to 1000 °C, the dissolubility of aluminosilicate in the red mud under high alkaline conditions increases firstly and then decreases after over 800 °C. Therefore, the optimum temperature of thermal treatment for red mud is about 800 °C. This study could contribute to the following preparation of geopolymeric material made from red mud, especially the pretreatment process of red mud.

Crystals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 115
Author(s):  
Suhail Huzaifa Jaafar ◽  
Mohd Hafiz Mohd Zaid ◽  
Khamirul Amin Matori ◽  
Sidek Hj. Ab Aziz ◽  
Halimah Mohamed Kamari ◽  
...  

This research paper proposes the usage of a simple thermal treatment method to synthesis the pure and Eu3+ doped ZnO/Zn2SiO4 based composites which undergo calcination process at different temperatures. The effect of calcination temperatures on the structural, morphological, and optical properties of ZnO/Zn2SiO4 based composites have been studied. The XRD analysis shows the existence of two major phases which are ZnO and Zn2SiO4 crystals and supported by the finding in the FT-IR. The FESEM micrograph further confirms the existence of both ZnO and Zn2SiO4 crystal phases, with progress in the calcination temperature around 700–800 °C which affects the existence of the necking-like shape particle. Absorption humps discovered through UV-Vis spectroscopy revealed that at the higher calcination temperature effects for higher absorption intensity while absorption bands can be seen at below 400 nm with dropping of absorption bands at 370–375 nm. Two types of band gap can be seen from the energy band gap analysis which occurs from ZnO crystal and Zn2SiO4 crystal progress. It is also discovered that for Eu3+ doped ZnO/Zn2SiO4 composites, the Zn2SiO4 crystal (5.11–4.71 eV) has a higher band gap compared to the ZnO crystal (3.271–4.07 eV). While, for the photoluminescence study, excited at 400 nm, the emission spectra of Eu3+ doped ZnO/Zn2SiO4 revealed higher emission intensity compared to pure ZnO/Zn2SiO4 with higher calcination temperature exhibit higher emission intensity at 615 nm with 700 °C being the optimum temperature. The emission spectra also show that the calcination temperature contributed to enhancing the emission intensity.


Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 579
Author(s):  
Sang-Ho Chung ◽  
Adrian Ramirez ◽  
Tuiana Shoinkhorova ◽  
Ildar Mukhambetov ◽  
Edy Abou-Hamad ◽  
...  

The Lebedev process, in which ethanol is catalytically converted into 1,3-butadiene, is an alternative process for the production of this commodity chemical. Silica–magnesia (SiO2–MgO) is a benchmark catalyst for the Lebedev process. Among the different preparation methods, the SiO2–MgO catalysts prepared by wet-kneading typically perform best owing to the surface magnesium silicates formed during wet-kneading. Although the thermal treatment is of pivotal importance as a last step in the catalyst preparation, the effect of the calcination temperature of the wet-kneaded SiO2–MgO on the Lebedev process has not been clarified yet. Here, we prepared and characterized in detail a series of wet-kneaded SiO2–MgO catalysts using varying calcination temperatures. We find that the thermal treatment largely influences the type of magnesium silicates, which have different catalytic properties. Our results suggest that the structurally ill-defined amorphous magnesium silicates and lizardite are responsible for the production of ethylene. Further, we argue that forsterite, which has been conventionally considered detrimental for the formation of ethylene, favors the formation of butadiene, especially when combined with stevensite.


2016 ◽  
Vol 2016 ◽  
pp. 1-11 ◽  
Author(s):  
C. O. Muga ◽  
Z. W. Zhang

Mg-Li based alloys are widely applied in various engineering applications. The strength of these alloys is modified and enhanced by different strengthening mechanisms. The strengthening mechanisms of these alloys and their composites have been extensively studied during the past decades. Important mechanisms applied to strengthening the alloys include precipitation strengthening, solution strengthening, grain and subgrain strengthening, and dislocation density strengthening. Precipitation and solution strengthening mechanisms are strongly dependent on composition of the alloys and thermal treatment processes, whereas grain and subgrain and dislocation density strengthening mechanisms majorly depend on thermomechanical processing. In this paper, recent studies on conventional processes for the strengthening of Mg-Li based alloys are summarized as they are critical during the alloys design and processing. Main strengthening mechanisms are objectively reviewed, focusing on their advantages and drawbacks. These can contribute to enhancing, initiating, and improving future researches for alloys design and suitable processing selection.


1999 ◽  
Vol 577 ◽  
Author(s):  
Q. Chen ◽  
B. M. Ma ◽  
B. Lu ◽  
M. Q. Huang ◽  
D. E. Laughlin

ABSTRACTThe phase transformation and the exchange coupling in (Ndo095Lao005)9.5FebaICOsNb 2BI05 have been investigated. Nanocomposites were obtained by treating amorphous precursors at temperatures ranging from 650TC to 9500C for 10 minutes. The magnetic properties were characterized via the vibrating sample magnetometer (VSM). X-ray diffraction (XRD), thermomagnetic analysis (TMA), and transmission electron microscopy (TEM) were used to perform phase identification, measure grain size, and analyze phase distribution. The strength of the exchange coupling between the magnetically hard and soft phases in the corresponding nanocomposite was analyzed via the AM-versus-H plot. It was found that the remanence (Br), coercivity (Hci), and maximum energy product (BHmax) obtained were affected by the magnetic phases present as well as the grain size of constituent phases and their distribution. The optimal magnetic performance, BHm, occurred between 700°C to 750°C, where the crystallization has completed without excessive grain growth. TMA and TEM indicated that the system was composed of three phases at this point, Nd2(Fe Co) 14B, ca-Fe, and Fe3B. The exchange coupling interaction among these phases was consistently described via the AM-versus-H plot up to 750°C. The Br, Hci, and BHmax degraded severely when the thermal treatment temperature increased from 750°C. This degradation may be attributed to the grain growth of the main phases, from 45 to 68nm, and the development of precipitates, which grew from 5nm at 750°C to 12nm at 850°C. Moreover, the amount of the precipitates was found to increase with the thermal treatment temperatures. The precipitates, presumably borides, may cause a decrease in the amount of the a-Fe and Fe 3B and result in a redistribution of the Co in the nanocomposites. The increase of the Co content in the Nd 2(Fe Co) 14B may explain the increase of its Curie temperature with the thermal treatment temperatures. In this paper, we examine the impacts of these factors on the magnetic properties of (Ndo 95Lao 05)9 5FebaICosNb2B10.5 nanocomposite.


JOM ◽  
1996 ◽  
Vol 48 (1) ◽  
pp. 25-28 ◽  
Author(s):  
Paolo Plescia ◽  
Dante Maccari

2017 ◽  
Vol 36 (3) ◽  
pp. 822-828
Author(s):  
SG Bawa ◽  
AS Ahmed ◽  
PC Okonkwo

Thermal stability of transitional alumina phases produced from ammonium alum using Kankara kaolin as starting material was studied. Wet beneficiation method was employed to purify the starting material, after which it was calcined and dealuminated with sulphuric acid. The elemental composition, mineralogical, and physiological analyses were carried out using X-ray fluorescence (XRF), X-ray diffraction (XRD) and Brunauer-Emmett-Teller (BET) techniques respectively. The ammonium alum was thermally treated by varying the calcination temperature from 700 to 1200°C and varying the time of calcination from 1 to 4 h. The formation of gamma alumina began at calcination temperature of 825°C for calcination time of 3 h, which was found to be lower than reported works of 900°C. It was found to be stable at higher temperature of 1125°C, above which phase transformation to alpha alumina was observed. The observed wide range of thermal stability of the gamma alumina phase gives it good advantage to be used for high temperature applications, such as support for catalyst promoters. Alpha alumina phase formation began at 1150°C and was fully formed at 1200°C. BET specific surface area of 166 m2/g was obtained for the gamma alumina phase which was high enough for it application as support for catalyst, catalyst and adsorbent. http://dx.doi.org/10.4314/njt.v36i3.23


2018 ◽  
Vol 6 (24) ◽  
pp. 11496-11506 ◽  
Author(s):  
Paul Pistor ◽  
Thomas Burwig ◽  
Carlo Brzuska ◽  
Björn Weber ◽  
Wolfgang Fränzel

We present the identification of crystalline phases by in situ X-ray diffraction during growth and monitor the phase evolution during subsequent thermal treatment of CH3NH3PbX3 (X = I, Br, Cl) perovskite thin films.


Author(s):  
Lawrence K. Wang ◽  
Clint Williford ◽  
Wei-Yin Chen ◽  
Nazih K. Shammas

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