scholarly journals Raman spectroscopy and X‐ray diffraction responses when measuring health‐related micrometre and nanometre particle size fractions of crystalline quartz and the measurement of quartz in dust samples from the cutting and polishing of natural and artificial stones

Author(s):  
Peter Stacey ◽  
Samantha Hall ◽  
Stephen Stagg ◽  
Francis Clegg ◽  
Christopher Sammon
Clay Minerals ◽  
1996 ◽  
Vol 31 (3) ◽  
pp. 417-422 ◽  
Author(s):  
H. M. Köster

AbstractMineralogical and chemical heterogeneity within three standard clay mineral samples have been identified by X-ray diffraction and chemical analysis of various size-fractions. This heterogeneity is partly attributed to accessory minerals, but mostly to structural and compositional variations in the 2:1 layer minerals of different particle size in the same specimen.


2012 ◽  
Vol 499 ◽  
pp. 72-75 ◽  
Author(s):  
Yan Lu

Using three natural graphites with different particle size, 35, 50 and 80 mesh, as raw materials, expandable graphites were prepared by intercalating, water-washing and drying the natural graphites. The products were characterized by X-ray diffraction, Infrared spectroscopy, scanning electron microscope and Raman spectroscopy. Results show that the structure of expandable graphite is affected strongly by the particle size of natural graphite. With increasing the particle size of natural graphite, for expandable graphite, the expansion degree of graphite flakes along the c-axis and the relative ratio of intercalating agents increase, while the structural disorder increases.


Clay Minerals ◽  
2008 ◽  
Vol 43 (3) ◽  
pp. 381-391 ◽  
Author(s):  
W. N. Mussel ◽  
E. Murad ◽  
P. S. R. Criscuolo ◽  
P. G. Pinheiro ◽  
J. D. Fabris

AbstractKaolin mined from the Ipixuna deposit of Pará Pigmentos S.A. in the Capim river area of northern Brazil has been studied at various stages of beneficiation to determine the behaviour of Fe- and Ti-bearing minerals which can reduce the brightness of the product. X-ray diffraction and Mössbauer spectroscopy showed the principal pigmenting minerals to be hematite and goethite, with chemical analyses showing a distinct decrease of both the total Fe and Ti contents in the course of processing. The Ti contents were primarily reduced due to the removal of anatase during particle size fractionation and dithionite reduction. While the Fe content of the final product is structurally bound in kaolinite, Raman spectroscopy indicates the remnant Ti to be bound both structurally in kaolinite and in remnant anatase.


Clay Minerals ◽  
2017 ◽  
Vol 52 (1) ◽  
pp. 83-95 ◽  
Author(s):  
R.A. Menezes ◽  
S.P.A. Paz ◽  
R.S. Angélica ◽  
R.F. Neves ◽  
R. Neumann ◽  
...  

AbstractUltramarine pigments were synthesized successfully from Na-A zeolite derived from kaolin waste. Na-A zeolite encapsulates the sulfur species formed and which act as chromophores, which circumvents their oxidation and the subsequent liberation of high levels of toxic gases during the reaction. Different Na-A zeolite matrices with various grain sizes (fine to coarse) were mixed with sulfur and sodium carbonate in various proportions to study the influence of these variables on the pigments’ colours and hues. After calcination at 500°C for 5 h, the products were characterized by X-ray diffraction, X-ray fluorescence and Raman spectroscopy and were classified by the Munsell system (colour and hue). Products with colour ranging from blue to green with various hues were obtained. Both colour and hue were affected by the amount of additives and by the particle size.


2005 ◽  
Vol 126 ◽  
pp. 101-105 ◽  
Author(s):  
B. Moulin ◽  
L. Hennet ◽  
D. Thiaudière ◽  
P. Melin ◽  
P. Simon

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 232
Author(s):  
Pedro J. Sánchez-Soto ◽  
Eduardo Garzón ◽  
Luis Pérez-Villarejo ◽  
George N. Angelopoulos ◽  
Dolores Eliche-Quesada

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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