首页> 美国政府科技报告 >Solvent Hold Tank Sample Results for Mcu-11-1452, Mcu-11-1453, Mcu-11-1454, Mcu-11-1455, Mcu-11-1456 and Mcu-11-1457
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Solvent Hold Tank Sample Results for Mcu-11-1452, Mcu-11-1453, Mcu-11-1454, Mcu-11-1455, Mcu-11-1456 and Mcu-11-1457

机译:mcu-11-1452,mcu-11-1453,mcu-11-1454,mcu-11-1455,mcu-11-1456和mcu-11-1457的溶剂保持罐样品结果

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Solvent Hold Tank (SHT) samples are sent to Savannah River National Laboratory (SRNL) to examine solvent composition changes over time. On December 5, 2011, Operations personnel delivered six samples from the SHT (MCU-11-1452 through -1457) for analysis. These samples are intended to verify that the solvent is within the specified composition range. The results from the analyses are presented in this document. Samples were received in p-nut vials containing (approx)10 mL each. Once taken into the Shielded Cells, the samples were combined. Samples were removed for analysis by density, semi-volatile organic analysis (SVOA), high performance liquid chromatography (HPLC), and Fourier-Transform Infra-Red spectroscopy (FTIR). Details for the work are contained in a controlled laboratory notebook. Each of the six p-nut vials contained a single phase, with no apparent solids contamination or cloudiness. Table 1 contains the results of the analyses for the combined samples. A duplicate density measurement of the organic phase gave a result of 0.844 g/mL (1.2% residual standard deviation - RSD). Using the density as a starting point, we know that the Isopar(reg sign) L should be slightly higher than nominal and the other components should be slightly lower than nominal. The results as a whole are internally consistent. All measurements indicate Isopar(reg sign) L higher than nominal, and Modifier lower than nominal. The extractant result is higher than expected - given the other results, the extractant concentration should be under nominal values. Using the measured density as well as the Isopar(reg sign) L and Modifier concentrations from the FTIR results, we calculate an extractant concentration of 6888 mg/L. This value is outside the analytical uncertainty of the reported HPLC value. Given the other results, this most likely indicates that the HPLC extractant result was biased high.

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