X-ray analysis of airborne particulates collected by an Andersen sampler. Compound and elemental distributions vs. particle size of laboratory particulates

The physical properties of ferrites are verysensitive to microstructure, which in turn critically dependson the manufacturing process.Nanocrystalline Lithium Stannoferrite system Li0.5+0.5XFe2.5-1.5XSnXO4,X= (0, 0.2, 0.4, 0.6, 0.8 and 1.0) fine particles were successfully prepared by double sintering ceramic technique at pre-sintering temperature of 500oC for 3 h andthepre-sintered material was crushed and sintered finally in air at 1000oC.The structural and microstructural evolutions of the nanophase have been studied using X-ray powder diffraction (XRD) and the Rietveld method.The refinement results showed that the nanocrystalline ferrite has a two phases of ordered and disordered phases for polymorphous lithium Stannoferrite.The particle size of as obtained samples were found to be ~20 nm through TEM that increases up to ~ 85 nmand isdependent on the annealing temperature. TEM micrograph reveals that the grains of sample are spherical in shape. (TEM) analysis confirmed the X-ray results.The particle size of stannic substituted lithium ferrite fine particle obtained from the XRD using Scherrer equation.Magneticmeasurements obtained from lake shoreâ€™s vibrating sample magnetometer (VSM), saturation magnetization ofordered LiFe5O8 was found to be (57.829 emu/g) which was lower than disordered LiFe5O8(62.848 emu/g).Theinterplay between superexchange interactions of Fe3+ ions at A and B sublattices gives rise to ferrimagnetic ordering of magnetic moments,with a high Curie-Weiss temperature (TCW ~ 900 K).

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Processing of granite quarry solid waste into industrial high silica materials using leaching process with HCl concentration variation

Jurnal Riset Teknologi Pencegahan Pencemaran Industri ◽

10.21771/jrtppi.2020.v11.no2.p43-50 ◽

2020 ◽

Vol 11 (2) ◽

pp. 43-50

Author(s):

Yusup Hendronursito ◽

Muhammad Amin ◽

Slamet Sumardi ◽

Roniyus Marjunus ◽

Frista Clarasati ◽

...

Keyword(s):

Particle Size ◽

Rotational Speed ◽

Inductively Coupled Plasma ◽

Chemical Elements ◽

Silica Content ◽

X Ray ◽

Concentration Variation ◽

Leaching Process ◽

Hcl Concentration ◽

Granite Powder

This study was aimed to increase granite's silica content using the leaching process with HCl concentration variation. The granite used in this study came from Lematang, South Lampung. This study aims to determine the effect of variations in HCl concentration, particle size, and rotational speed on the crystalline phase and chemical elements formed in the silica product produced from granite. The HCl concentration variations were 6.0 M, 7.2 M, 8.4 M, and 9.6 M, the variation in particle size used was 270 and 400 mesh. Variations in rotational speed during leaching were 500 and 750 rpm. Granite powder was calcined at 1000 ºC for 2 hours. Characterization was performed using X-Ray Fluorescence (XRF), X-Ray Diffraction (XRD), and Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP- OES). The results showed that the silica content increased with increasing HCl concentration, the finer the particle size, and the higher the rotational speed. XRF analysis showed that the silica with the highest purity was leached with 9.6 HCl with a particle size of 400 mesh and a rotational speed of of 750 rpm, which was 73.49%. Based on the results above, by leaching using HCl, the Si content can increase from before. The XRD diffractogram showed that the granite powder formed the Quartz phase.

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Modification of Wood with Monoethanolamino-borate by The Data of X-Ray Photoelectron Spectroscopy

MATEC Web of Conferences ◽

10.1051/matecconf/201819604005 ◽

2018 ◽

Vol 196 ◽

pp. 04005

Author(s):

Irina Stepina ◽

Irina Kotlyarova

Keyword(s):

Particle Size ◽

Photoelectron Spectroscopy ◽

Model Compound ◽

Hydrolytic Stability ◽

Photoelectron Spectra ◽

Wood Cellulose ◽

Rapid Loss ◽

X Ray ◽

Wood Protection ◽

Cellulose Materials

The difficulty of wood protection from biocorrosion and fire is due to the fact that modifiers in use are washed out from the surface of the substrate under the influence of environmental factors. This results in a rapid loss of the protective effect and other practically important wood characteristics caused by the modification. To solve this problem is the aim of our work. Here, monoethanolaminoborate is used as a modifier, where electron-donating nitrogen atom provides a coordination number equal to four to a boron atom, which determines the hydrolytic stability of the compounds formed. Alpha-cellulose ground mechanically to a particle size of 1 mm at most was used as a model compound for the modification. X-ray photoelectron spectra were recorded on the XSAM-800 spectrometer (Kratos, UK). Prolonged extraction of the modified samples preceded the registration of the photoelectron spectra to exclude the fixation of the modifier molecules unreacted with cellulose. As a result of the experiment, boron and nitrogen atoms were found in the modified substrate, which indicated the hydrolytic stability of the bonds formed between the modifier molecules and the substrate. Therefore monoethanolaminoborate can be considered as a non-extractable modifier for wood-cellulose materials.

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X-ray studies of particle size in silica

Journal of the Franklin Institute ◽

10.1016/s0016-0032(29)90939-x ◽

1929 ◽

Vol 208 (1) ◽

pp. 59-71

Author(s):

R.H. Aborn ◽

R.L. Davidson

Keyword(s):

Particle Size ◽

X Ray

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

Minerals ◽

10.3390/min11030232 ◽

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.

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Review of Respirable Coal Mine Dust Characterization for Mass Concentration, Size Distribution and Chemical Composition

Minerals ◽

10.3390/min11040426 ◽

2021 ◽

Vol 11 (4) ◽

pp. 426

Author(s):

Behrooz Abbasi ◽

Xiaoliang Wang ◽

Judith C. Chow ◽

John G. Watson ◽

Bijan Peik ◽

...

Keyword(s):

Mass Spectrometry ◽

Particle Size ◽

Real Time ◽

Coal Mine ◽

Energy Dispersive ◽

Size Distributions ◽

X Ray ◽

Membrane Filters ◽

Mine Dust ◽

Mass Concentrations

Respirable coal mine dust (RCMD) exposure is associated with black lung and silicosis diseases in underground miners. Although only RCMD mass and silica concentrations are regulated, it is possible that particle size, surface area, and other chemical constituents also contribute to its adverse health effects. This review summarizes measurement technologies for RCMD mass concentrations, morphology, size distributions, and chemical compositions, with examples from published efforts where these methods have been applied. Some state-of-the-art technologies presented in this paper have not been certified as intrinsically safe, and caution should be exerted for their use in explosive environments. RCMD mass concentrations are most often obtained by filter sampling followed by gravimetric analysis, but recent requirements for real-time monitoring by continuous personal dust monitors (CPDM) enable quicker exposure risk assessments. Emerging low-cost photometers provide an opportunity for a wider deployment of real-time exposure assessment. Particle size distributions can be determined by microscopy, cascade impactors, aerodynamic spectrometers, optical particle counters, and electrical mobility analyzers, each with unique advantages and limitations. Different filter media are required to collect integrated samples over working shifts for comprehensive chemical analysis. Teflon membrane filters are used for mass by gravimetry, elements by energy dispersive X-ray fluorescence, rare-earth elements by inductively coupled plasma-mass spectrometry and mineralogy by X-ray diffraction. Quartz fiber filters are analyzed for organic, elemental, and brown carbon by thermal/optical methods and non-polar organics by thermal desorption-gas chromatography-mass spectrometry. Polycarbonate-membrane filters are analyzed for morphology and elements by scanning electron microscopy (SEM) with energy dispersive X-ray, and quartz content by Fourier-transform infrared spectroscopy and Raman spectroscopy.

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Synthesis of magnesium carbonate hydrate from natural talc

Open Chemistry ◽

10.1515/chem-2020-0154 ◽

2020 ◽

Vol 18 (1) ◽

pp. 951-961

Author(s):

Qiuju Chen ◽

Tao Hui ◽

Hongjuan Sun ◽

Tongjiang Peng ◽

Wenjin Ding

Keyword(s):

Crystal Structure ◽

Particle Size ◽

Crystal Growth ◽

Crystal Morphology ◽

Magnesium Carbonate ◽

Organic Additives ◽

X Ray Diffraction ◽

Morphological Transformation ◽

X Ray ◽

Carbonation Process

AbstractVarious morphologies of magnesium carbonate hydrate had been synthesized without using any organic additives by carefully adjusting the reaction temperature and time during the talc carbonation process. At lower temperatures, magnesium carbonate hydrate was prone to display needle-like morphology. With the further increase of the carbonation temperature, the sheet-like crystallites became the preferred morphology, and at higher aging temperatures, these crystallites tended to assemble into layer-like structures with diverse morphologies, such as rose-like particles and nest-like structure. The reaction time had no effect on the crystal morphology, but it affected the particle size and situation of the crystal growth. X-Ray diffraction results showed that these various morphologies were closely related to their crystal structure and compositions. The needle-like magnesium carbonate hydrate had a formula of MgCO3·3H2O, whereas with the morphological transformation from needle-like to sheet-like, rose-like, and nest-like structure, their corresponding compositions also changed from MgCO3·3H2O to 4MgCO3·Mg(OH)2·8H2O, 4MgCO3·Mg(OH)2·5H2O, and 4MgCO3·Mg(OH)2·4H2O.

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Synthesis and Advanced Characterization of Polymer-Protein Core-Shell Nanoparticles

Catalysts ◽

10.3390/catal11060730 ◽

2021 ◽

Vol 11 (6) ◽

pp. 730

Author(s):

Erik Sarnello ◽

Tao Li

Keyword(s):

Particle Size ◽

Small Angle ◽

Core Shell ◽

Assembly Process ◽

Shell Nanoparticles ◽

X Ray ◽

X Ray Scattering ◽

Wide Range ◽

Core Shell Nanoparticles ◽

Ray Scattering

Enzyme immobilization techniques are widely researched due to their wide range of applications. Polymer–protein core–shell nanoparticles (CSNPs) have emerged as a promising technique for enzyme/protein immobilization via a self-assembly process. Based on the desired application, different sizes and distribution of the polymer–protein CSNPs may be required. This work systematically studies the assembly process of poly(4-vinyl pyridine) and bovine serum albumin CSNPs. Average particle size was controlled by varying the concentrations of each reagent. Particle size and size distributions were monitored by dynamic light scattering, ultra-small-angle X-ray scattering, small-angle X-ray scattering and transmission electron microscopy. Results showed a wide range of CSNPs could be assembled ranging from an average radius as small as 52.3 nm, to particles above 1 µm by adjusting reagent concentrations. In situ X-ray scattering techniques monitored particle assembly as a function of time showing the initial particle growth followed by a decrease in particle size as they reach equilibrium. The results outline a general strategy that can be applied to other CSNP systems to better control particle size and distribution for various applications.

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