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THE APPLICATION OF MÖSSBAUER CASSITERITE ANALYSER FOR THE
APPROXIMATE ANALYSIS OF TIN CONTAINING ORES OF MIXED COMPOSITION
I. Garsanov, V. Labushkin, E. Makarov
To cite this version:
I. Garsanov, V. Labushkin, E. Makarov. THE APPLICATION OF MÖSSBAUER CASSI- TERITE ANALYSER FOR THE APPROXIMATE ANALYSIS OF TIN CONTAINING ORES OF MIXED COMPOSITION. Journal de Physique Colloques, 1980, 41 (C1), pp.C1-477-C1-478.
�10.1051/jphyscol:19801188�. �jpa-00219677�
JOURNAL DE PHYSIQUE Colloque Cl , suppl6ment au n O 1, Tome 41, janvier 1980, page Cl-477
THE APPLICATION OF MSSBAUER CASSITERITE ANALYSER FOR THE APPROXIMTE ANALYSIS OF T I N CONTAINING ORES OF MIXED CWPOSITION
I.Ya. Garsanov, v.G. Labushkin, E.F. Makarov
AZZ-Union Research Institute of Physico-TechnicaZ and RadiotechnicaZ Measurements, Moscow, USSR.
One of the practical applications of the ~$ssbauer effect involves the approxi- mate analysis of tin-containing ores
&-a
The t&6ssbauer cassiterite analyser was reported[2]to be developed in which a re- sonanse ionization chamber was used as a detector. The application of the resonan- ce method of registering the .scattered radiation from the sample permitted the instrument characteristics to be substan- tially improved
[3] .
A new modification of the instrument with the logic elements in its circuitry has an upgraded reliabi- lity and stability.In the analysis o f tin-containing ores the content of oxidized tin can be rciscal culated due to the so-called matrix effect arising from the different influence of the filler composition on the radiation intensity analysed. It was reported [I] that the results of measurement of the cassiterite concentration are independent of the filler composition when measured by means of a non-resonant detector.
It is seen from our investigations (Fig. I) that the instruments employing the resonance methods of radiation detec- tion show the strong dependence of the quantity measured
&h%
(where I,I00
Pig. I. The dependence E=F(C) for the samples with Si02
sand
Fe 0 matrices.2 3
and loo are the ioniziation current va- lues at the source velocity V=O and V= 00
on the concentration of impurity elements in the sample. It should be pointed out that in order to determine the cassiteri- te concentration by the instruments of this ty-pe, they must be preliminarily ca- librated against the standarts which are usually the powder samples of Imown cassi- terite contenk and whose filler compositi- on may differ from that .of real samples.
To eliminate the influence of impurity elements on the accuracy of cassiterite content measurements the selective filters were deposited in a d e f a t e sequence on the input window of the detector unit.
These filters absorb the fluorescent ra-
Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/jphyscol:19801188
c1-478 JOURNAL DE PHYSIQUE
diation from t h e impurity elements lying within t h e energy range from 4.5 t o I1 k6V
Ihe efficiency of a f i l t e r system con- s i s t i n g of t h i n / IO mg/cm2 / layers Ca&!i!i02+Cr 2 3 0 i s demonstrated by the example of an iron-containing matrix since iron i s the major impurity element in t i n ores.(Pig. 2)
Pig. 2 The amplitude spectra of t h e radiation from the source scattered by the Fe 0 m a t r i x (with 1% Sn02)
2 3
The multi-layer f i l t e r (CaQcTiO2+Cr2O3) made it possible t o get rid of the back- ground component of the ionisation current ewoed by t h e interaction of the fluorescent X-ray radiation with the re- sonance radiator substance depo- s i t e d on the electrode p l a t e s of a reso- nance ionization &ember and having t h e excitation potential of Lsn t i n l i n e between 3.9 and 4.4 keV.
Curve 3 of Fig. I was obtained f o r a powder sample with Fe 0 matrix using the
2 3
f i l t e r s described above. It coincided with t h e calibration curve I obtained f o r t h e
standard c a s s i t e r i t e samples in t h e Si02
samples can be cancelled, u t i l i z i n g t h e resonance method of registering t h e
Gesbauer radiation of the sample and e l i - minatibg the fluorescent X-ray l i n e s of impurity elements from the spectrum of scattered radiation.
Iief erences
[I]
Gamma resonauce methods and instru- ments used i n t h e analysis of physes of the mineral raw materials.Atomizdaht
,
1974.[2] Garzanov, I .Pa. ,Karlashchub,V. I., KO- telnikov,V.A., Labushkin,V.G., Maka- rov,E.P., Proceedings of the !jth In- ternational conference on S s s b a u e r spectroscopy, Bratislava. Part 3.
1973, 660.
[j] The K W R instrument. The advertisement leaf l e t . ~ t a n d a r t g h i z
.
1978,matrix.
Thus, t h e influence of t h e matrix being the mador source of systematic e r z o ~ 6 i n c a s s i t e r i t e content measarrements of r e a l