Abstract
BackgroundAmine degradation products are very important for industrials not only leads to amine losses but also contribute to operational problems such as high corrosion effects. In this research, a new quantitative method has been developed for the analysis of 2-methylaminoethanol (MAE) and tris(2-hydroxyethylethyl)ethylenediamine (THEED) in the diethanolamine solution by cation-exchange chromatography. MethodsThe mobile phase was optimized for the interference-free determination of THEED and MAE. For THEED, the final composition was included 8 mmol L−1 HNO3 and 15% (v/v) acetonitrile. The linear range of the calibration curve was achieved in the range of 0.5 to 1000 ppm with the correlation coefficient of 0.9998. The relative standard deviation was 3.89%. Also, the mobile phase was optimized for MAE determination. The optimal composition was 1.45 mmol L−1 of HNO3, 0.15 mmol L−1 of 18-crown-6, and 3.4 mmol L−1 of dipicolinic acid. The mobile phase also was contained 0.75% (v/v) of acetonitrile. Significant FindingsThe linear range of the calibration curve was from 0.1 to 200 ppm with a correlation coefficient of 0.9999, and the relative standard deviation is 0.46%. Very low detection limits including 0.03 and 0.17 ppm were found for MAE and THEED respectively. Acceptable precisions, below the 3.89%, were accomplished by the method. The proposed method was used for the determination of desired compounds in the real natural gas sweetening solution.
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