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EMISSION SPECTRAL METHODS

Semiquantitative emission spectral analysis (SQESA)

Until the present, this method has been a universal express method used at all stages of geological surveys and exploration to determine more than 30 elements with contents from 10-6-10-5% to 10%, although it is inferior to chemical analysis in accuracy. SQESA can be extremely effective as a preceding one for choosing the optimal quantitative method (assessment of matrix composition, level of elements of interest, presence of interfering elements and their grade). The Laboratory uses two versions of this method, which differ in the way of sample introduction into the arc discharge: evaporation from the carbon electrode channel and sample powder spilling into the arc discharge. The option of evaporation from the electrode channel is preferable for determining elements with high vapour pressure (so-called “difficultly volatile”: Zr, Hf, Nb, Ta, Be, REE, U, Th), as well as in the case of a small amount of sample material; the spill option is characterized by lower detection limits of so-called “easily volatile” elements (Ag, As, Cu, Cd, Bi, Ge, In, Pb, Sb, Te, Tl, Zn) and the best reproducibility of the analysis results compared to channel evaporation. The accuracy of both SQESA options is category V according to OST 41-08-212-82.

Minimum analytical aliquot: 30 mg for evaporation from the electrode channel; 400 mg for spilling.


Content Intervals determined by SQESA


Component to be determined

Evaporation from the channel

Spilling

SiO2
Al2O3
MgO
CaO
Fe2O3
K2O
Na2O
P2O5
TiO2
MnO

0.01 - 50 %
0.01 - 30 %
0.01 – 40 %
0.01 – 20 %
0.01 – 40 %
0.08 – 10 %
0.01 – 10 %
0.08 – 20 %
0.01 – 20 %
0.005 – 10 %


 

 

 

 

 
0.02– 20 %
0.0001– 10 %
0.0001 – 10 %

ppm

ppm

Sr
Ba
V
Cr
Co
Ni
Zr
Hf
Nb
Ta
Sc
Ce
La
Y
Yb
U
Th
Be
Li
W
Mo
Sn
Cu
Pb
Zn
Cd
Bi
Ag
Ge
Ga
Tl
As
Sb
Te
B

100 – 100000 
10 – 100000 
2 – 10000 
1 – 30 000 
1 – 1 000 
1 – 30000 
10 – 3 000 
10 – 100 
80 –300 
100 – 1 000 
1– 100 
10 – 1 000 
10 – 1 000 
1 – 1000 
0.5 – 100 
300 – 10000 
100 – 3 000 
0.5 – 300 
10 – 3 000 
5 – 1 000 
0,5 – 10000 
2 – 3 000 
0.5 – 80 000 
2 – 100000 
10 – 80 000 
3 – 1 000 
2 – 300 
0.03 – 1000 
2 – 100 
2 –  300 
10 – 300 
100 – 80 000 
20 – 80 000 
30 – 300 
5 – 10000 

50 – 100000 
50 – 100000 
1 – 10000 
1 – 30000 
0,5 – 2000 
0,5– 30000 
20 – 3000 

5 – 1 000 

2 – 100 
50 – 1000 
10 – 1 000 
1 – 1 000 
1 – 100 


0,5 – 300 
10 – 3 000 
0,5– 1 000 
0,5 – 10000 
0,5 – 3 000 
0,5– 80 000 
1 – 8 000 
10 – 80 000 
0,5– 1000 
1 –  300 
0.01 – 1000 
0,5 – 100 
1 – 300 

2 – 80 000 
10 – 80 000 

5 – 10 000 


Note: 1 ppm = 1´10-4%

The Laboratory also performs SQESA of minerals (rock-forming and ore-bearing) and rocks from microaliqouts from 1 mg. Conditions and details of this kind of analyses should be previously agreed by the Customer with the Laboratory management.

Basic physical and chemical methods of analysis

Main physicochemical methods used in the CL include inductively coupled plasma atomic emission spectrometry and mass spectrometry (ICP AES and ICP MS), as well as atomic absorption spectrometry (AAS). Objects to be analyzed are water samples (potable, natural, waste) and powder samples of rock, ore, soils, bottom sediment. Before being analized, such samples must be transferred to the solution.


Main methods of sample decomposition and transfer to the solution

The following dissolution techniques are used:

  1. The method of sample decomposition by fusion is based on complete dissolution of a sample in a fusing agent (flux) - lithium metaborate - and the transference of the resulting mixture of solid complex oxides to the solution by nitric acid and is intended for various types of rocks and soils. It should be noted that the processing of the sample by fusion with lithium metaborate ensures complete determination of elements, particularly rare earths present in stable phases, and this is the main difference between the fusion and acid decomposition. For fusion, we use muffle furnaces and platinum or graphite crucibles; the Classe Fluxer-Bis automatic unit manufactured by Labortechnik GmbH (Germany) with gold-platinum crucibles is also used.
  2. The method of “complete” sample decomposition with a mixture of concentrated acids and oxidizing agents is based on reactions of the interaction of sample components with acids to form salts soluble in dilute nitric acid. Acid decomposition is carried out in polytetrafluoroethylene utensils on electric stoves with automatic temperature control, or using ETHOS PLUS microwave ovens from Milestone S.r.I., which provide almost complete sample solubilization. Aliquots vary from 0.05 to 1 g.
  3. The method of sample decomposition by aqua regia is based on the same principles as method 2, however, in this case, only partial transfer of most of the components into the solution is possible. The silicate part is not decomposed that leads to the underestimation of values for rock-forming elements. The procedure is conducted in heat-resistant glassware.

For sample decomposition and preparing solutions, we use High Pure acids with additional purification - distillation using BSB-939-IR manufactured by Laborprodukte GmbH., Germany, and highly purified deionized water (water purification station made by Labconco, the USA). Quantitative emission spectral analysis (QESA).


Inductively coupled plasma atomic emission spectrometry

The NPTIMA-8300 ICP spectrometer manufactured by Perkin-Elmer (2017) with improved technical characteristics provides high measurement accuracy and reliable results, improved detection limits and an extended dynamic range.


Optima 8300 Inductively Coupled Plasma Atomic Emission Spectrometer

The CL uses the methodology developed and certified by the VSEGEI CL: VSEGEI MP No. 11/2010 “Determination of macro- and microelements in rock, soil, ore, bottom sediment samples with inductively coupled plasma atomic emission spectrometry, third category of accuracy.


Lower determination limits achieved with the OPTIMA-8300:

No

Element

Range, % wt

No

Element

Range, % wt

Minimum

Maximum

Minimum

Maximum

1

2

3

4

5

6

7

8

9

10

11

12

13

14

15

16

Al

Ag

Ba

Be

Bi

Са

Cd

Co

Cr

Cu

Fe

Ga

Ge

K

Li

Mg

0.01

0.0001

0.0003

0.00005

0.0002

0.01

0.00005

0.00005

0.0001

0.0001

0.01

0.0001

0.0001

0.01

0.0001

0.001

30

0.1

1

1

1

50

0.1

1

1

1

80

0.1

0.1

10

1

50

17

18

19

20

21

22

23

24

25

26

27

28

29

30

Mn

Mo

Na

Ni

P

Pb

Sb

Sc

Si

Sn

Sr

Ti

V

Zn

0.001

0.00005

0.01

0.0001

0.001

0.0001

0.0002

0.00002

0.01

0.0004

0.00001

0.001

0.0001

0.0001

10

1

10

1

2

1

1

0.1

80

1

1

10

1

1

Note: 1% = 1000 ppm
Яндекс.Метрика