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Yun-jun JIANG, Xing LI, Hai-lun JIANG, Ning ZHANG, Xue HAN, Yong-xiao ZHU. Determination of Sulfur in Soil by Inductively Coupled Plasma-Optical Emission Spectrometry with Four Acids Open Dissolution[J]. Rock and Mineral Analysis, 2018, 37(2): 152-158. DOI: 10.15898/j.cnki.11-2131/td.201704010048
Citation: Yun-jun JIANG, Xing LI, Hai-lun JIANG, Ning ZHANG, Xue HAN, Yong-xiao ZHU. Determination of Sulfur in Soil by Inductively Coupled Plasma-Optical Emission Spectrometry with Four Acids Open Dissolution[J]. Rock and Mineral Analysis, 2018, 37(2): 152-158. DOI: 10.15898/j.cnki.11-2131/td.201704010048

Determination of Sulfur in Soil by Inductively Coupled Plasma-Optical Emission Spectrometry with Four Acids Open Dissolution

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  • Received Date: April 09, 2017
  • Revised Date: December 21, 2017
  • Accepted Date: March 20, 2018
  • Published Date: February 28, 2018
  • HIGHLIGHTS
    (1) Sulfur in soil samples can be well dissolved by HCl-HNO3-HF-HClO4 acid system.
    (2) Sulfur and K, Na, Ca, Mg or other elements in the solution can be simultaneously measured by ICP-OES.
    (3) In this method, a solution can simultaneously determine more than 15 kinds of elements with high analytical efficiency.
    At present, sulfur in soil is mainly determined by X-ray Fluorescence Spectrometry and tube furnace combustion iodine methods. The analysis speed of these two methods is slow, and the analysis accuracy is poor for both high and low content samples, difficult to meet the requirements of accurate and rapid determination of many samples. In order to improve the speed and accuracy of analysis, a new method for the determination of sulfur in soil samples by Inductively Coupled Plasma-Optical Emission Spectrometry combined with four acids digestion was developed. In this paper the digestion effect of aqua regia, aqua hot water bath and HCl-HNO3-HF-HClO4 is compared. The four acids digestion method was proven to better dissolve sulfur in soil samples. The method is simple, rapid and accurate with a low detection limit of 10 μg/g, analysis range between 33.3 μg/g and 50000 μg/g, and relative standard deviation between 0.47% and 4.05%. Many elements such as potassium, sodium, calcium, magnesium, iron, manganese, beryllium, lithium, lanthanum, cerium, scandium, vanadium, cobalt, nickel, and titanium can be determined simultaneously in a solution without increasing analysis cost. The method, which has been verified with actual samples, is suitable for application in the geological industry.

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