Table 1. Method Performance and Concentrations of N-Nitrosamines in U.S. Biosolids.
recovery (%)b |
biosolids
concentration (ng/g) avg. (min, max)c |
||||||||
---|---|---|---|---|---|---|---|---|---|
compound | CAS# | molecular weight (g/mol) | absolute | relative | method detection limit (ng/g dw) | wet weight | dry weight | RPDd (%) | detection frequency (%) |
NDMA | 62-75-9 | 74 | 32 ± 12 | 110 ± 11 | 5.7 | 150 (54, 248) | 504 (87, 920) | 34 | 3 |
NMEAa | 10595-95-6 | 88 | 32 ± 7 | 1.1 | 11.4 (5.5, 14) | 121 (20, 393) | 12 | 5 | |
NDPA | 621-64-7 | 130 | 41 ± 12 | 100 ± 5 | 0.6 | 44 (2.4, 314) | 134 (7, 505) | 46 ± 20 | 21 |
NDBAa | 924-16-3 | 158 | 38 ± 14 | 0.1 | 0.7 (0.2, 1.9) | 1.8 (0.2, 3.3) | 21 ± 23 | 9 | |
NPYRa | 930-55-2 | 100 | 51 ± 8 | 2.3 | 3.8 | 7.6 | 15 | 1 | |
NPIP | 100-75-4 | 114 | 52 ± 7 | 100 ± 4 | 1.1 | 78 (12, 224) | 332 (51, 1185) | 15 | 11 |
NDPhA | 86-30-6 | 198 | 68 ± 18 | 90 ± 10 | 0.06 | 4.5 (0.1, 91) | 10 (0.7, 147) | 23 ± 29 | 79 |
Concentrations of analytes lacking stable-isotope labeled analogues are not recovery corrected.
Relative recoveries were determined using area ratios of analyte to (stable-isotope labeled) surrogate standard. Absolute recoveries were obtained using absolute areas instead of area ratios. Absolute recoveries were determined from matrix spike studies.
Dry weight concentrations were calculated from wet weight concentrations using the solids content of the biosolids samples.
RPD: relative percentage difference.