scholarly journals Pharmaceutical and Physico Chemical Analysis of Tuttha Bhasma

2021 ◽  
pp. 1-8
Author(s):  
Anjana V Mani ◽  
R Rajam
Keyword(s):  
Chemical Analysis ◽  
Copper Sulphate ◽  
Hexagonal Lattice ◽  
Particle Size Analysis ◽  
Sodium Sulphate ◽  
Nano Particles ◽  
Size Analysis ◽  
Particle Analysis ◽  
X Ray ◽  
Physico Chemical

Rasa sastra is an ancient science dealing with various drugs of mineral and metallic origin Tuttha (copper sulphate) is a mineral useful in various clinical conditions externally as well as internally. According to Rasasastra, through the process of Shodhana (purification) and Marana (incineration) the harmful effects of Tuttha bhasma (incinerated copper sulphate) is nullified resulting in the formation of a newer compound that is therapeutically more potent. To prepare Tuttha Bhasma by adopting standard manufacturing procedure explained in Ayurvedic texts as well as to study it’s physical and chemical characters using traditional and modern analytical tools. The pharmaceutical processing of Tuttha bhasma was carried out in three Kukkuta puta (incineration) with a peak temperature of 6100C according to Rasa Tarangini reference. Physico chemical analysis, Energy-Dispersive X-ray Fluorescence (EDXRF), X-ray Diffraction (XRD), Particle Size Analysis (PSA) were conducted. The final product shows presence of nano particles which was confirmed by particle analysis. XRD results of Tuttha bhasma revealed the presence of copper sulphide (covellite) with hexagonal lattice and sodium sulphate with orthorhombic structure. All of the preparation stages and changes in the properties were documented and validated, and they may now be used as a valuable tool for standardization and quality assurance of Tuttha bhasma.

scholarly journals CHARACTERIZATION OF TAILINGS FROM THE PROCESSING OF ORNAMENTAL ROCKS

2021 ◽  
pp. 103-116
Author(s):  
Antonio Augusto Sousa ◽  
Hilda Camila Nogueira ◽  
Gabriela de Castro Araújo ◽  
Felipe Augusto Sousa ◽  
Alisson Rufino Andrade
Keyword(s):  
Particle Size ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Limiting Factor ◽  
X Ray Diffraction ◽  
X Ray ◽  
Physical Chemical ◽  
Physico Chemical ◽  
Cosmetic Industry ◽  
Alternative Material

The processing of ornamental rocks promotes the constant generation of abrasive sludge, which, in turn, causes different types of contamination. The possibility of reusing residues generated in industrial processes has economic advantages, therefore, it is necessary to know the physical, chemical and mineral properties of these residues. Thus, the objective of this research was to evaluate the possibilities of application of abrasive mud, generated in industries located in the city of Campina Grande - PB, based on its main characteristics. The methodology consisted of the following analyzes: X-ray fluorescence, X-ray diffraction, scanning electron microscopy, particle size analysis and physical-chemical analysis. Chemical analyzes revealed that the residues have interesting characteristics, mainly for use in civil construction. The mineralogical analysis indicated that the sample has an essential mineral composition for the cosmetic industry, which was confirmed by the detected elements present. The study of the particle size characterized the sample as material of irregular shape and with good micronization, confirming the potential for reuse as a cosmetic, while the morphological analysis showed the presence of iron as a limiting factor for certain applications. Physico-chemical tests confirmed the characteristics common to abrasive sludge. The characterized samples showed, in general, satisfactory properties with regard to its use as an alternative material in different segments.

scholarly journals Characteristics of some clay materials from Tamilnadu, India, and their possible ceramic uses

Cerâmica ◽  
2012 ◽  
Vol 58 (347) ◽  
pp. 412-418 ◽  
Author(s):  
C. Manoharan ◽  
P. Sutharsan ◽  
S. Dhanapandian ◽  
R. Venkatachalapathy
Keyword(s):  
Particle Size Analysis ◽  
Size Analysis ◽  
Loss On Ignition ◽  
X Ray Diffraction ◽  
Low Loss ◽  
Red Clay ◽  
Moderate Amount ◽  
X Ray ◽  
High Loss ◽  
Physico Chemical

X-ray fluorescence, themogravimetric-differential thermal analysis, Fourier Transform Infrared spectroscopy, X-ray diffraction, particle size analysis and Atterberg limits were used to study physico-chemical, mineralogical and thermal properties of two types of clays from four different locations of Tamilnadu, India. The chemical and mineralogical compositions of these clays differ considerably. The mineralogy indicated that the alluvial clays (G1 and G2) comprise highly quartz, illite, kaolinite, plagioclase and small amount of chlorite. The red clays (R1 and R2) were also rich in quartz, well-ordered kaolinite and abundant Fe-bearing minerals such as goethite and hematite. With respect to chemical composition, the G1 and G2 clays contained high amount of SiO2, low amount of Al2O3 and low loss on ignition, however, the R1 and R2 clays contain moderate amount of SiO2, Al2O3, and high amount of Fe2O3 and high loss on ignition. The results indicate that clays from alluvial deposit have adequate characteristics for common brick fabrication. However, clays collected from red clay deposit possessing adequate properties for roofing tile manufacturing and can be used for the manufacturing of common brick with some modification.

scholarly journals Mining Wastes of an Albite Deposit as Raw Materials for Vitrified Mullite Ceramics

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 232
Author(s):  
Pedro J. Sánchez-Soto ◽  
Eduardo Garzón ◽  
Luis Pérez-Villarejo ◽  
George N. Angelopoulos ◽  
Dolores Eliche-Quesada
Keyword(s):  
Particle Size ◽  
Raw Materials ◽  
Phase Evolution ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Mining Wastes ◽  
X Ray Diffraction ◽  
X Ray ◽  
Maximum Value

In this work, an examination of mining wastes of an albite deposit in south Spain was carried out using X-ray Fluorescence (XRF), X-ray diffraction (XRD), particle size analysis, thermo-dilatometry and Differential Thermal Analysis (DTA) and Thermogravimetric (TG) analysis, followed by the determination of the main ceramic properties. The albite content in two selected samples was high (65–40 wt. %), accompanied by quartz (25–40 wt. %) and other minor minerals identified by XRD, mainly kaolinite, in agreement with the high content of silica and alumina determined by XRF. The content of Na2O was in the range 5.44–3.09 wt. %, being associated with albite. The iron content was very low (<0.75 wt. %). The kaolinite content in the waste was estimated from ~8 to 32 wt. %. The particle size analysis indicated values of 11–31 wt. % of particles <63 µm. The ceramic properties of fired samples (1000–1350 °C) showed progressive shrinkage by the thermal effect, with water absorption and open porosity almost at zero at 1200–1250 °C. At 1200 °C, the bulk density reached a maximum value of 2.38 g/cm3. An abrupt change in the phase evolution by XRD was found from 1150 to 1200 °C, with the disappearance of albite by melting in accordance with the predictions of the phase diagram SiO2-Al2O3-Na2O and the system albite-quartz. These fired materials contained as main crystalline phases quartz and mullite. Quartz was present in the raw samples and mullite was formed by decomposition of kaolinite. The observation of mullite forming needle-shape crystals was revealed by Scanning Electron Microscopy (SEM). The formation of fully densified and vitrified mullite materials by firing treatments was demonstrated.

Preparation of xanthated bentonite and its removal behavior for Pb(II) ions

2010 ◽  
Vol 61 (5) ◽  
pp. 1235-1243 ◽  
Author(s):  
Y. F. He ◽  
F. R. Li ◽  
R. M. Wang ◽  
F. Y. Li ◽  
Y. Wang ◽  
...  
Keyword(s):  
Adsorption Mechanism ◽  
Removal Rate ◽  
Freundlich Isotherm ◽  
Particle Size Analysis ◽  
Lead Ions ◽  
Size Analysis ◽  
Optimum Conditions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir

Xanthate was successfully grafted onto bentonite by a relatively simple solution reaction. The obtained xanthated bentonite (XBent) was characterized by FT-IR spectrophotometer, thermogravimetric analysis (TG), particle size analysis, x-ray diffraction (XRD) and scanning electron microscopy (SEM). XBent acting as a type of environmentally friendly adsorbent was applied to remove lead ions from aqueous solutions. The optimum conditions were as follows: [Pb2 + ] = 500 mg L−1, [XBent] = 2 g L−1, pH = 5.0; oscillating 60 min under 200 rpm at 25°C. The removal rate of lead was up to 99.9%. It was found that the lead(II) ions—XBent adsorption isotherm model fitted well to the Freundlich isotherm. The adsorption mechanism was also investigated by SEM and XRD, which concluded that lead ions were complexed or chelated with XBent. XBent appears to have potential to be used later in water treatment as a type of inorganic polymer reagent.

scholarly journals Recycling of Waste Solution after Hydrothermal Conversion of Fly Ash on a Semi-Technical Scale for Zeolite Synthesis

Materials ◽  
2021 ◽  
Vol 14 (6) ◽  
pp. 1413
Author(s):  
Rafał Panek ◽  
Jarosław Madej ◽  
Lidia Bandura ◽  
Grzegorz Słowik
Keyword(s):  
Fly Ash ◽  
Nitrogen Adsorption ◽  
Particle Size Analysis ◽  
Al2o3 Content ◽  
Size Analysis ◽  
Zeolite Synthesis ◽  
Hydrothermal Conversion ◽  
Waste Solution ◽  
X Ray ◽  
X Zeolites

Nowadays, using fly ash for zeolites production has become a well-known strategy aimed on sustainable development. During zeolite synthesis in a hydrothermal conversion large amount of post-reaction solution is generated. In this work, the solution was used as a substrate for Na-A and Na-X zeolites synthesis at laboratory and technical scale. Obtained materials were characterized using particle size analysis, X-ray diffraction (XRD), X-ray fluorescence spectroscopy (XRF), transmission electron microscopy (TEM), Fourier transformed infrared spectroscopy (FTIR), and nitrogen adsorption/desorption isotherm. Produced zeolites revealed high purity (>98%) and monomineral zeolitic phase composition. The SiO2 content was in the range 39–42% and 40–38%, whereas Al2O3 content was 23–22% and 25–26% for Na-X and Na-A, respectively. TEM and BET analyses revealed Na-X zeolite pores were almost identical to commercial 13X with SBET in the range 671–734 m2/g. FTIR indicated slight differences between materials obtained at laboratory and technical scale in Si-O-(Si/Al) bridges of the zeolitic skeleton. The results showed good replicability of the laboratory process in the larger scale. The proposed method allows for waste solution reusability with a view to highly pure zeolites production in line with circular economy assumptions.

Synthesis of Alpha-Tricalcium Phosphate by Wet Reaction and Evaluation of Mechanical Properties

2012 ◽  
Vol 727-728 ◽  
pp. 1164-1169 ◽  
Author(s):  
Mônica Beatriz Thürmer ◽  
Rafaela Silveira Vieira ◽  
Juliana Machado Fernandes ◽  
Wilbur Trajano Guerin Coelho ◽  
Luis Alberto Santos
Keyword(s):  
Mechanical Properties ◽  
Calcium Phosphate ◽  
Tricalcium Phosphate ◽  
Calcium Nitrate ◽  
Chemical Precipitation ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Calcium Phosphate Cements

Calcium phosphate cements have bioactivity and osteoconductivity and can be molded and replace portions of bone tissue. The aim of this work was to study the obtainment of α-tricalcium phosphate, the main phase of calcium phosphate cement, by wet reaction from calcium nitrate and phosphoric acid. There are no reports about α-tricalcium phosphate obtained by this method. Two routes of chemical precipitation were evaluated and the use of two calcinations temperatures to obtain the phase of cement. The influence of calcination temperature on the mechanical properties of cement was evaluated. Cement samples were characterized by particle size analysis, X-ray diffraction, mechanical strength and scanning electron microscopy. The results demonstrate the strong influence of synthesis route on the crystalline phases of cement and the influence of concentration of reactants on the product of the reaction, as well as, on the mechanical properties of cement.

X-ray fluorescence spectrometry for rapid screening of particle size in soils

2021 ◽  
Author(s):  
Maame Croffie ◽  
Paul N. Williams ◽  
Owen Fenton ◽  
Anna Fenelon ◽  
Karen Daly
Keyword(s):  
Particle Size ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
Soil Texture ◽  
Particle Size Analysis ◽  
Parent Material ◽  
Fluorescence Spectrometry ◽  
Rapid Screening ◽  
Size Analysis ◽  
X Ray

&lt;p&gt;Soil texture is an essential factor for effective land management in agricultural production. Knowledge of soil texture and particle size at field scale can aid with on-going soil management decisions. Standard soil physical and gravimetric methods for particle size analysis are time-consuming and X-ray fluorescence spectrometry (XRF) provides a rapid and cost-effective alternative. The objective of this study was to explore the use of XRF as a predictor for particle size. An extensive archive of Irish soils with particle size and soil texture data was used to select samples for XRF analysis. Regression and correlation analyses on XRF determined results showed that the relationship between Rb and % clay varied with soil type and was dependent on the parent material. There was a strong relationship (R &gt; 0.62, R&lt;sup&gt;2&lt;/sup&gt;&gt;0.30, p&lt;0.05) between Rb and clay for soils originating from bedrock such as limestones and slate. Contrastingly, no significant relationship (R&lt;0.03, R&lt;sup&gt;2&lt;/sup&gt;=0.00, p&gt;0.05) exists between Rb and % clay for soils originating from granite and gneiss. Furthermore, there was a significant negative correlation (p&lt;0.05) between Rb and % sand. The XRF is a useful technique for rough screening of particle size distribution in soils originating from certain parent materials. Thus, this may contribute to the rapid prediction of soil texture based on knowledge of the particle size distribution.&lt;/p&gt;&lt;p&gt;&amp;#160;&lt;/p&gt;

scholarly journals СИНТЕЗ И ИССЛЕДОВАНИЕ СТЕКЛООБРАЗОВАНИЯ В СИСТЕМЕ AS2S3-ERS

2021 ◽  
Vol 7 (5(59)) ◽  
pp. 28-31
Author(s):  
ТЕЙМУР МАМЕД ИЛЬЯСЛИ ◽  
ДУНИЯ ТАЛЕХ ГАСАНОВА ◽  
ИМИР ИЛЬЯС АЛИЕВ
Keyword(s):  
Chemical Analysis ◽  
Solid Solutions ◽  
Glass Formation ◽  
Room Temperature ◽  
Slow Cooling ◽  
X Ray ◽  
Physico Chemical

To determine the area of glass formation in the system As2S3-ErS were synthesized alloys in the range of concentrations 0-30 mol. % ErS. The methods of physico-chemical analysis of differential-thermal (DTA), X-ray phase (RFA), microstructural (MCA) analyzes, as well as the measurement of microhardness and density determined the area of the glass and studied them physicо-chemical propertes. It is established that in the system As2S3-ErS on the basis of As2S3 during slow cooling the area of the glass reaches 17 mol. % ErS. Alloys in the concentration range 20-30 mol. % ErS are glass-crystalline. In the system at room temperature solid solutions on the basis of As2S3 are distributed up to 2.5 mol.% ErS, and on the basis of solid solutions ErS are practically not installed.

scholarly journals Synthesis of SnO2 Nanoparticles by High Potential Electrolysis

2017 ◽  
Vol 12 (2) ◽  
pp. 281 ◽  
Author(s):  
Fredy Kurniawan ◽  
Rahmi Rahmi
Keyword(s):  
Particle Size ◽  
Sno2 Nanoparticles ◽  
Particle Size Analysis ◽  
Reaction Engineering ◽  
High Potential ◽  
Size Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nanoparticles Synthesis ◽  
The Fourier Transform

SnO2 nanoparticles have been synthesized by high voltage electrolysis. Tin bare was used for anode and cathode. The effect of potentials and electrolyte were studied. The particles obtained after electrolysis was characterized using X-ray Diffraction (XRD). The diffractogram is in agreement with the standard diffraction pattern of SnO2 which is identified as tetragonal structure. The Fourier Transform Infrared (FTIR) spectrum indicates that there is a vibration of Sn–O asymmetric at 580 cm-1. The optimum potential for SnO2 nanoparticles synthesis is 60 V at 0.06 M HCl which shows the highest UV-Vis spectrum. The absorption peak of SnO2 nanoparticles by UV-Vis spectrophotometer appears at about 207 nm. The particle size analysis shows that the SnO2 nanoparticles obtained have the size distribution in a range of 25-150 nm with the highest volume at 83.11 nm. Copyright © 2017 BCREC Group. All rights reservedReceived: 15th November 2016; Revised: 26th February 2017; Accepted: 27th February 2017How to Cite: Rahmi, R., Kurniawan, F. (2017). Synthesis of SnO2 Nanoparticles by High Potential Electrolysis. Bulletin of Chemical Reaction Engineering & Catalysis, 12 (2): 281-286 (doi:10.9767/bcrec.12.2.773.281-286)Permalink/DOI: http://dx.doi.org/10.9767/bcrec.12.2.773.281-286 

The Evaporative Decomposition of Solutions Method (Eds) for the Production of Ultrafine Y1Ba2Cu3O7 from Nitrate and Mixed Anion Precursor Solutions

1989 ◽  
Vol 169 ◽  
Author(s):  
Rollin E. Lakis ◽  
Sidney R. Butler
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Barium Carbonate ◽  
Hollow Spheres ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron

AbstractY1Ba2Cu3O7 has been prepared by the evaporative decomposition of solutions method. Nitrate and mixed anion solutions were atomized and decomposed at temperatures ranging from 300°C to 950°C. The resulting materials have been characterized using x-ray powder diffraction, Thermal Gravimetric Analysis (TGA), particle size analysis, Scanning Electron Microscopy (SEM), and Transmission Electron Microscopy (TEM). The powder consists of 0.3 micron agglomerated hollow spheres with a primary particle size of 0.06 micron. TGA and x-ray diffraction indicate the presence of barium nitrate and barium carbonate due to incomplete decomposition and/or product contamination by the process environment.

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