蓝鲸体育直播

Generally, Atomic Absorption Instrument (AA) or Inductivity Coupled Plasma-Optical Emission Spectrometry Instrument (ICP-OES) is used to measure potassium ion, first by extracting the potassium ion from sample soils by 1 mol/L ammonium acetate CH₃COONH₄. These are the methods performed in laboratories.

We have developed a method for a rapid measurement of potassium ion in various soils by the use of small and affordable instrument LAQUAtwin potassium ion meter K-11 (Ion Selective Electrode Method). The extraction method is the same as the lab method, which the high concentration existence of CH₃COONH₄ will affect the measurement result as the ammonium ion in the extraction solution is an interferring ion for the potassium measurement. The following procedure explains how this effect can be reduced to obtain a correlative result as the lab method.

銆怣easurement procedure銆�

1. Put 1g each of air-dried soils (four samples) in 100mL glass beakers, two beakers per soil sample.
2. Prepare two kinds of extraction per soil sample, one by adding 20 ml of 1mol/L CH₃COONH₄ to one beaker, and 20ml of 0.01mol/L CH₃COONH₄ to another beaker. 
3. Shake the beakers around 1 hour to extract K⁺ from the soil by the use of Petit Bath Shaker Model 2220 made by Wakenyaku Company of Japan.
4. Calibrate LAQUAtwin K-11 with 150mg/L and 2000mg/L K⁺ standard solutions included in the product.
5. Measure potassium ion concentration of the filtrated solution with calibrated K-11 and with ICP-OES (蓝鲸体育直播 Jobin Yvon. Model ULTIMA2).
6. Perform this measurement with 4 different samples.

*Although the measurement range of K-11 is between 40 mg/L to 4000 mg/L K⁺, K-11 can perform theoretically down to 4mg/L K⁺.

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Table 1 shows the results from ICP-OES and LAQUAtwin K⁺ extracted with 1 mol/L and 0.01 mol/L CH₃COONH₄.

Figure 1 shows the potassium extraction efficiency measured with ICP-OES. Setting 1 mol/L CH₃COONH₄ extraction as 100%, efficiency trend is plotted depending on different CH₃COONH₄ concentration. 

Figure 2 shows the correlation between ICP-OES and LAQUAtwin K⁺measurements with 0.01 mol/L CH₃COONH₄ extraction. 

Based on table 1, higher value against ICP-OES is detected by LAQUAtwin K⁺ with 1 mol/L CH₃COONH₄ extraction, due to strong interference by NH+ of CH₃COONH₄. However, with 0.01 mol/L CH₃COONH₄ extraction, although the extraction efficiency is reduced by approximately 80%^* (Figure 1), very good correlation (R=0.981锛孯²=0.962) is obtained between ICP-OES and LAQUAtwin (Figure 2).

*Extraction efficiencies will vary amongst soil samples.

罢补产濒别锛戯细碍⁺ concentrations measured by ICP-OES and LAQUAtwin extracted with 1 mol/L CH₃COONH₄ and 0.01 mol/L CH₃COONH₄. 

锛圲nit : mg/L锛�

Fig.1锛歏ariation of extraction efficiency with CH₃COONH₄ concentration. 

*Extraction efficiencies will vary amongst soil samples.

Fig.2 Relation between measured values of K⁺ (mol/L) by ICP-OES and by LAQUAtwin.

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