Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Comparison of soil sample preparation methods in determining mobile element species by inductively coupled plasma optical emission spectrometry. / Савинов, Сергей Сергеевич; Тлеужанова, Рабига.
в: Journal of Analytical Chemistry, Том 81, № 3, 01.03.2026, стр. 424-431.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
}
TY - JOUR
T1 - Comparison of soil sample preparation methods in determining mobile element species by inductively coupled plasma optical emission spectrometry
AU - Савинов, Сергей Сергеевич
AU - Тлеужанова, Рабига
N1 - Savinov S.S., Tleuzhanova R.D. Comparison of soil sample preparation methods in determining mobile element species by inductively coupled plasma optical emission spectrometry // Journal of analytical chemistry. 2026, v. 81, is. 3, p. 424-431. DOI: 10.1134/S1061934825701680
PY - 2026/3/1
Y1 - 2026/3/1
N2 - Abstract: Soil serves as a linking component in ecosystems; because of its high sorption capacity, it retains various elements, regulates their transfer into natural waters, and controls their availability in the nutrient medium of plants. Determination of the content of mobile element species in soil relies on their extraction with an ammonium acetate buffer solution, which presents one of the most widely used extractants, followed by an analysis of the resulting extract. Experimental results demonstrate that matrix effects during the application of the ICP OES method can manifest themselves differently for different soil samples. Analysts can eliminate these effects by the fivefold dilution of the extract; however, some samples require higher dilution factors. The known certified procedures for determining mobile species describe various approaches to obtaining ammonium acetate extracts. Experimental data demonstrate the influence of analyte extraction schemes differing in the time of interaction between the soil aliquot and the extracting solution, mixing method, and the number of extraction stages. On average, after 24-h equilibration, twice as much of the mobile element species is extracted as after 1-h agitation of the suspension on a shaker. In addition, the extraction efficiency depends both on the nature of the specific analyte and on the soil under investigation.
AB - Abstract: Soil serves as a linking component in ecosystems; because of its high sorption capacity, it retains various elements, regulates their transfer into natural waters, and controls their availability in the nutrient medium of plants. Determination of the content of mobile element species in soil relies on their extraction with an ammonium acetate buffer solution, which presents one of the most widely used extractants, followed by an analysis of the resulting extract. Experimental results demonstrate that matrix effects during the application of the ICP OES method can manifest themselves differently for different soil samples. Analysts can eliminate these effects by the fivefold dilution of the extract; however, some samples require higher dilution factors. The known certified procedures for determining mobile species describe various approaches to obtaining ammonium acetate extracts. Experimental data demonstrate the influence of analyte extraction schemes differing in the time of interaction between the soil aliquot and the extracting solution, mixing method, and the number of extraction stages. On average, after 24-h equilibration, twice as much of the mobile element species is extracted as after 1-h agitation of the suspension on a shaker. In addition, the extraction efficiency depends both on the nature of the specific analyte and on the soil under investigation.
KW - heavy metals
KW - matrix effects in ICP OES
KW - mobile metal species in soils
KW - soil sample preparation
UR - https://www.mendeley.com/catalogue/a814bc5c-ec2f-3210-8a90-0ba5656d3c85/
U2 - 10.1134/s1061934825701680
DO - 10.1134/s1061934825701680
M3 - Article
VL - 81
SP - 424
EP - 431
JO - Journal of Analytical Chemistry
JF - Journal of Analytical Chemistry
SN - 1061-9348
IS - 3
Y2 - 19 May 2025 through 23 May 2025
ER -
ID: 151445587