Abstract
Abstract In crops of the sugarcane, the concentrations of molybdenum (Mo) in the leaves are generally lower than 0.3 mg Mo kg−1. These low concentrations have resulted in limitations in the methods and instruments that can be used for these analyses. The objective of this study was to evaluate three different techniques to determine the concentration of Mo in sugarcane leaves sampled in the principal sugarcane‐producing areas in Brazil. Two spectrometric techniques were evaluated by using ICP‐EAS (Inductively Coupled Plasma‐Emission Automated System) and DCP‐MEAS (Direct Coupled Plasma–Multiple Emission Automated System) and a colorimetric technique of the reaction between potassium iodide and hydrogen peroxide (KI‐H2O2). The techniques ICP‐EAS and KI‐H2O2 produced results of satisfactory accuracy and precision, whereas the DCP‐MEAS consistently overestimated the Mo concentrations in cane leaves. The KI‐H2O2 technique showed sensitivity 5 times greater than the ICP‐EAS, with minimum detection limits of 0.1 and 0.5 mg Mo kg−1, respectively.
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Claims 4
Claim · model-written summary
ICP-EAS and KI-H2O2 gave satisfactory accuracy and precision for Mo in sugarcane leaves.
Verbatim
e1“produced results of satisfactory accuracy and precision”
t0“Sugarcane”
Claim · model-written summary
DCP-MEAS consistently overestimated Mo concentrations in cane leaves.
Verbatim
e1“consistently overestimated the Mo concentrations in cane leaves”
Claim · model-written summary
The KI-H2O2 technique was 5 times more sensitive than ICP-EAS.
Verbatim
e1“showed sensitivity 5 times greater”
t0“Sugarcane”
Claim · model-written summary
Minimum detection limits were 0.1 mg Mo kg-1 for KI-H2O2 and 0.5 mg Mo kg-1 for ICP-EAS.
Verbatim
e1“minimum detection limits of 0.1 and 0.5 mg Mo kg−1”
t0“Sugarcane”