scholarly journals Extração Hidrometalurgica do potássio presente na rocha Nefelina-Sienito, em função da variação da granulometria e aplicação de tratamento térmico.

2020 ◽  
Vol 1 (49) ◽  
pp. 129
Author(s):  
Defsson Douglas de Araújo Ferreira ◽  
Danúbio Leonardo Bernardino de Oliveira ◽  
João Batista de Sousa Santos ◽  
Vinícius Rewel do Nascimento Cordeiro
Keyword(s):  
Grain Size ◽  
Citric Acid ◽  
Chemical Composition ◽  
Thermal Treatment ◽  
Calcination Temperature ◽  
Mineral Processing ◽  
Agricultural Industry ◽  
Different Temperatures ◽  
The City

<p class="Normal1">Rocks that contain minerals with potassium in their chemical composition, such as, for example, Sienito and Nefelina-Sienito, are an alternative and potentially viable source for extraction of this element, however, for structural reasons this potassium is insoluble and can not be absorbed by plants. Considering that Brazil imports almost as much potassium as the agricultural industry requires, it is necessary to look for alternative ways and routes to take advantage of potentially producing sources. In this sense, a route of mineral processing and metallurgical extraction was proposed in order to make the K present in the Nefelina-Sienito rocks extracted in the city of Pedra Lavrada/PB soluble and usable. The methodology used was to apply thermal treatment and hydrometallurgical extraction with citric acid to analyze the solubility of potassium in two granulometric ranges defined by the granulochemical characterization carried out initially. The results of the granulochemical analysis showed that the highest concentrations of the element of interest were in the bands: retained in 200 and passed through 200 meshes. However, the results of the metallurgical extraction as a function of the different temperatures showed that the highest percentage of solubility (7.68%) was for samples with a grain size less than 200 mesh and a calcination temperature of 1000 ° C.</p>

scholarly journals Effects of Framework Disruption of Ga and Ba Containing Zeolitic Materials by Thermal Treatment

Catalysts ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 975
Author(s):  
Siyabonga S. Ndlela ◽  
Holger B. Friedrich ◽  
Mduduzi N. Cele
Keyword(s):  
Thermal Treatment ◽  
Calcination Temperature ◽  
Lewis Acid ◽  
Acid Sites ◽  
Deep Oxidation ◽  
Isomorphic Substitution ◽  
Lewis Acid Sites ◽  
Different Temperatures ◽  
Strong Lewis Acid ◽  
Zeolitic Materials

The effect of the thermal treatment of some zeolitic materials was studied on oxidative dehydrogenation (ODH) of n-octane. Gallium containing faujasite catalysts were synthesized using isomorphic substitution, specifically, a galosilicalite (Ga-BaY(Sil)) and an aluminosilicalite substituted with gallium (Ga-BaY(IS)), with constant Si/M ratio. The catalysts were thermally treated at different temperatures (250, 550, and 750 °C) before catalytic testing. The quantification of total and strength of acid sites by FT-IR (O-H region), pyridine-IR, and NH3-temperature-programmed desorption (TPD) confirmed a decrease in the number of Brønsted acid sites and an increase in the number of Lewis acid sites upon increasing the calcination temperature. Isothermal n-octane conversion also decreased with the catalysts’ calcination temperature, whereas octene selectivity showed the opposite trend (also at iso-conversion). The COx selectivity showed a decrease over the catalysts calcined from 250 to 550 °C and then an increase over the 750 °C calcined catalysts, which was due to the strong adsorption of products to strong Lewis acid sites on the catalysts leading to the deep oxidation of the products. Only olefinic-cracked products were observed over the 750 °C calcined catalysts. This suggested that the thermal treatment increases Lewis acid sites, which activate n-octane using a bimolecular mechanism, instead of a monomolecular mechanism.

scholarly journals Effect of Calcination Temperature on Structural Properties and Photocatalytic Activity of Ceria Nanoparticles Synthesized Employing Chitosan as Template

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Angela B. Sifontes ◽  
Maibelin Rosales ◽  
Franklin J. Méndez ◽  
Olycen Oviedo ◽  
Tamara Zoltan
Keyword(s):  
Photocatalytic Activity ◽  
Thermal Treatment ◽  
Calcination Temperature ◽  
Structural Properties ◽  
Visible Light Irradiation ◽  
Azo Dye ◽  
Ceria Nanoparticles ◽  
Catalyst Amount ◽  
Different Temperatures ◽  
Degradation Reaction

Ceria nanoparticles were synthesized employing chitosan as template and thermal treatment at different temperatures (350, 650, and 960°C). The effect of calcination temperature on structural properties and photocatalytic activity of ceria nanopowder was also tested. Degradation of an azo dye, Congo Red (CR) as a model aqueous pollutant, was investigated by means of photocatalysis of ceria nanoparticles under visible light irradiation. The influence of catalyst amount, initial CR concentrations, and degradation reaction kinetics were studied. The results were compared with commercial CeO2at the same degradation conditions.

scholarly journals Effect of calcination temperature on neptunium dioxide microstructure and dissolution

2020 ◽  
Vol 7 (12) ◽  
pp. 3869-3876
Author(s):  
Kathryn M. Peruski ◽  
Brian A. Powell
Keyword(s):  
Grain Size ◽  
Free Energy ◽  
Surface Area ◽  
Calcination Temperature ◽  
Surface Free Energy ◽  
Neptunium Dioxide

Solubility of neptunium dioxide decreases as microstructure grain size increases, likely due to decreasing surface free energy and surface area.

scholarly journals Influence of Calcination Temperature on Crystal Growth and Optical Characteristics of Eu3+ Doped ZnO/Zn2SiO4 Composites Fabricated via Simple Thermal Treatment Method

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 ◽  
...  
Keyword(s):  
Thermal Treatment ◽  
Band Gap ◽  
Calcination Temperature ◽  
Emission Intensity ◽  
Emission Spectra ◽  
Treatment Method ◽  
Absorption Bands ◽  
Vis Spectroscopy ◽  
Doped Zno ◽  
Zno Crystal

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.

scholarly journals Changes of Physicochemical Properties of Starch Syrups Recommended for Winter Feeding of Honeybees during Storage

Agriculture ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 374
Author(s):  
Teresa Szczęsna ◽  
Ewa Waś ◽  
Piotr Semkiw ◽  
Piotr Skubida ◽  
Katarzyna Jaśkiewicz ◽  
...  
Keyword(s):  
Chemical Composition ◽  
Physicochemical Properties ◽  
Physicochemical Parameters ◽  
Storage Temperature ◽  
Storage Conditions ◽  
Different Temperatures ◽  
And Storage ◽  
Bee Colonies ◽  
Temperature Time ◽  
Winter Feeding

The aim of this study was to determine the influence of storage temperature and time on physicochemical parameters of starch syrups recommended for the winter feeding of bee colonies. The studies included commercially available three starch syrups and an inverted saccharose syrup that were stored at different temperatures: ca. 20 °C, 10–14 °C, and ca. 4 °C. Physicochemical parameters of fresh syrups (immediately after purchase) and syrups after 3, 6, 9, 12, 15, 18, 21, and 24 months of storage at the abovementioned temperatures were measured. It was observed that the rate of unfavorable changes in chemical composition of starch syrups and the inverted saccharose syrup, mainly the changes in the 5-hydroxymethylfurfural (HMF) content, depended on the type of a syrup and storage conditions (temperature, time). Properties of tested starch syrups intended for winter feeding of bees stored at ca. 20 °C maintained unchanged for up to 6 months, whereas the same syrups stored at lower temperatures (10–14 °C) maintained unchanged physicochemical parameters for about 12 months. In higher temperatures, the HMF content increased. To date, the influence of this compound on bees has not been thoroughly investigated.

scholarly journals The Importance of Thermal Treatment on Wet-Kneaded Silica–Magnesia Catalyst and Lebedev Ethanol-to-Butadiene Process

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 579
Author(s):  
Sang-Ho Chung ◽  
Adrian Ramirez ◽  
Tuiana Shoinkhorova ◽  
Ildar Mukhambetov ◽  
Edy Abou-Hamad ◽  
...  
Keyword(s):  
Thermal Treatment ◽  
Calcination Temperature ◽  
Catalytic Properties ◽  
Catalyst Preparation ◽  
Preparation Methods ◽  
Calcination Temperatures ◽  
Alternative Process ◽  
Magnesium Silicates

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.

A Study on The Phase Transformation and Exchange-Coupling of (Nd0 95La0 05)9 5FebalCo5Nb2B10.5 Nanocomposites

1999 ◽  
Vol 577 ◽  
Author(s):  
Q. Chen ◽  
B. M. Ma ◽  
B. Lu ◽  
M. Q. Huang ◽  
D. E. Laughlin
Keyword(s):  
Grain Size ◽  
Magnetic Properties ◽  
Phase Transformation ◽  
Thermal Treatment ◽  
Grain Growth ◽  
Exchange Coupling ◽  
Phase Distribution ◽  
Maximum Energy ◽  
Treatment Temperature ◽  
Phase Identification

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.

scholarly journals Using Diaper Waste to Prepare Magnetic Catalyst for the Synthesis of Glycerol Carbonate

2020 ◽  
Vol 2020 ◽  
pp. 1-9
Author(s):  
Jincan Wang ◽  
Yong Liang ◽  
Song Wang ◽  
Patrick U. Okoye ◽  
Hongxu Chen ◽  
...  
Keyword(s):  
Magnetic Property ◽  
Calcination Temperature ◽  
Separation Process ◽  
Nickel Nitrate ◽  
Glycerol Carbonate ◽  
Magnetic Catalyst ◽  
Catalyst Separation ◽  
Different Temperatures

Diaper waste was calcined above 400°C after impregnated in the solution of nickel nitrate. The as-prepared diaper waste-derived materials were used as magnetic catalysts for the synthesis of glycerol carbonate (GC). Structure and catalytic ability investigations on the catalysts calcined at different temperatures indicated that calcination temperature was an important factor affecting the property of catalysts. It was found that the catalyst obtained at the calcination temperature of 700°C (named DW-Ni-700) showed the best performance. When DW-Ni-700 was used in the synthesis of GC, GC yield reached 93.2%, and the magnetic property of DW-Ni-700 facilitated the catalyst separation process. Meanwhile, DW-Ni-700 showed high reusability in the reaction. After four times reuse of DW-Ni-700, GC yield decreased less than 4%.

Molecular Interactions Investigation of L-Histidine in Water and in Aqueous Citric Acid at Different Temperatures Using Volumetric and Acoustic Methods

2018 ◽  
Vol 232 (3) ◽  
pp. 393-408 ◽  
Author(s):  
Dinesh Kumar ◽  
Shashi Kant Sharma
Keyword(s):  
Citric Acid ◽  
Molar Volume ◽  
Atmospheric Pressure ◽  
Apparent Molar Volume ◽  
Adiabatic Compressibility ◽  
Acid Solutions ◽  
Solvent Interactions ◽  
Intermolecular Free Length ◽  
Acoustic Methods ◽  
Different Temperatures

AbstractDensities,ρand ultrasonic speeds, u of L-histidine (0.02–0.12 mol·kg−1) in water and 0.1 mol·kg−1aqueous citric acid solutions were measured over the temperature range (298.15–313.15) K with interval of 5 K at atmospheric pressure. From these experimental data apparent molar volume ΦV, limiting apparent molar volume ΦVOand the slopeSV, partial molar expansibilities ΦEO, Hepler’s constant, adiabatic compressibilityβ, transfer volume ΦV, trO, intermolecular free length (Lf), specific acoustic impedance (Z) and molar compressibility (W) were calculated. The results are interpreted in terms of solute–solute and solute–solvent interactions in these systems. It has also been observed that L-histidine act as structure maker in water and aqueous citric acid.

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