Usability of field X-ray fluorescence analyzers for determination of the chemistry of cement raw materials - using an example of Mokrá Quarry

Author(s):  
Jiří Zimák ◽  
Kristýna Dalajková ◽  
Roman Donocik ◽  
Petr Krist ◽  
Daniel Reif ◽  
...  
Keyword(s):  
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.


1962 ◽  
Vol 28 (2) ◽  
pp. 234-238 ◽  
Author(s):  
Edward J. Olsen

AbstractThe X-ray spectrometer method as an archaeological tool is discussed with special reference to its limitations as a chemical analytical instrument. Qualitative results are presented for six North American copper samples, one European trade brass, and nine artifacts from the Great Lakes region. From this pilot study it is concluded that the most fruitful results in the problem of the determination of provenance of copper artifacts will be obtained from semi-quantitative optical spectographic analyses of carefully collected artifacts and raw materials. The largest inherent error in this problem is that of meaningful sampling techniques. The only recourse is to treat such chemical data statistically and determine the probabilities that given specimens came from the various possible sources.


2021 ◽  
Vol 87 (8) ◽  
pp. 19-22
Author(s):  
D. G. Filatova ◽  
A. A. Arkhipenko ◽  
M. A. Statkus ◽  
I. V. Mikheev ◽  
V. B. Baranovskaya ◽  
...  

An approach to the simultaneous isolation of As (III) and Se (IV) from solutions on a new S,N-containing sorbent followed by determination of the analyte in the sorbent phase using total reflection X-ray fluorescence (TXRF) has been proposed. To match the goal, a sorbent with a branched structure was synthesized on the base of polyacrylamide modified with formaldehyde and hydrogen sulfide. This is a heteroatomic copolymer containing sulfide bridges in the chain and crosslinking by a tertiary amine. Conditions for the quantitative co-extraction of As (III) and Se (IV), i.e., sorption in solutions of 1 M HNO3 with calcium ions present, heating to 60°C and phase contact time of 1 h were determined. The mechanism of sorption interaction of the analytes under specified conditions is discussed. It is shown that a 100-fold excess of iron, zinc and copper does not interfere with the extraction of analytes, thus providing the possibility of As (III) and Se (IV) isolation from different types of raw materials and processed products using the synthesized sorbent. A method for the direct XRF quantification of arsenic and selenium with sr 0.09 and 0.08, respectively, in the sorbent phase has been developed. The correctness of the results was confirmed by the ICP-MS method in analysis of aqueous reference solution after dissolution of the sorbate in HNO3 (1:1).


1970 ◽  
Vol 19 (6) ◽  
pp. 812-818
Author(s):  
Hiroshi UCHIKAWA ◽  
Masahiro NUMATA
Keyword(s):  

2018 ◽  
Vol 284 ◽  
pp. 1018-1023
Author(s):  
A.V. Khandoshka ◽  
Svetlana G. Vlasova

The composition of mineral wool was selected for the research, based on the chemical composition of the raw materials, the determination of the acidity module to obtain the thermal insulation material with the best characteristics and the lowest cost of the production of basalt mineral wool. The paper deals with compositions of raw materials and selection chemical compositions of charges for production of basalt mineral wool, and the experiments of welded samples were made and tested for viscosity, surface tension, chemical analysis and x-ray analysis.


Author(s):  
Jiří Zimák ◽  
Kristýna Dalajková ◽  
Roman Donocik ◽  
Petr Krist ◽  
Daniel Reif ◽  
...  
Keyword(s):  

1975 ◽  
Vol 19 ◽  
pp. 203-212
Author(s):  
W. T. Harter

The U. S. Steel Research x-ray spectrometric laboratory performs between 7,000 and 10,000 analytical determinations each month for alloying elements in all types of steels and raw -materials. The spectrometer is automatically controlled by a DEC PDP 8/1 minicomputer utilizing vari ations of software packages provided by Siemens Corporation. As many as 256 individual analytical measurements can be sequentially performed. The minimal interelemental effects encountered in low-alloy steel analyses are corrected in a separate program written in FOCAL language. Correction coefficients for the program were established by multiple linear regression analyses.Stainless and multialloy steels are analyzed with a two-part control and correction program. The control program controls all functions of the spectrometer automatically and stores parabolic calibration coefficients. Following a sequential determination of the alloying elements control is switched to a correction program written in FOCAL. The correction program prints a tabular listing of the elements determined, followed by a listing of the corrected concentrations of elements adjusted for interelemental effects. Orthogonal polynomial analyses were performed to determine σ values for all constituents determined.For analysis of raw materials, the samples are fused prior to analysis by use of a flux and heavy absorber technique that essentially eliminates interelement effects and permits linear calibrations up to 100 percent. Samples are ground and pelletized after fusion for better reproducibility. Single sets of calibration standards are used regardless of raw materials mineralogical history. Synthetic standards can be produced for ranges where no calibration standards exist.


1970 ◽  
Vol 19 (11) ◽  
pp. 1476-1487 ◽  
Author(s):  
Hiroshi UCHIKAWA ◽  
Masahiro NUMATA ◽  
Tokio OKAWA ◽  
Takaichi SUNADA
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document