Indian River Research and Education Center, University of Florida/IFAS, 2199 South Rock Road, Fort Pierce, FL 34945-3138, USA.
Sci Total Environ. 2011 Aug 15;409(18):3482-91. doi: 10.1016/j.scitotenv.2011.04.032.
A rapid ultrasonic extraction method coupled with a heated-copper clean-up procedure for removing interfering constituents was developed for analyzing pyrethroid and phenylpyrazole pesticides in sediments. Incubation of the 60 mL extract with 12 g copper granules at 60 °C for 2h was determined to be the optimal conditions for removing the interfering constituents. Eleven pyrethroid and phenylpyrazole pesticides were spiked into sediment samples to determine the effectiveness of the ultrasonic extraction method. The average recoveries of pyrethroids and phenylpyrazoles in sediment at 4 °C storage on day 0, 1, 7, 14, and 21 ranged from 98.6 to 120.0%, 79.2 to 116.0%, 85.0 to 119.7%, 93.6 to 118.7%, and 92.1 to 118.2%, respectively, with all percent relative standard deviations less than 10% (most <6%). This illustrated the stability of pyrethroids and phenylpyrazoles in sediment during sediment aging at 4 °C. Recoveries of the pesticides ranged from 98.6% to 120.0% for lowest fortification level (2-16 μg kg⁻¹), from 97.8% to 117.9% for middle fortification level (10-80 μg kg⁻¹), and from 94.3% to 118.1% for highest fortification level (20-160 μg kg⁻¹). Relative standard deviations of pesticide recoveries were usually less than 7%. Method detection limits of target pesticides ranged from 0.22 μg kg⁻¹ to 3.72 μg kg⁻¹. Furthermore, field sediment samples collected from four residential lakes during a three-month monitoring period were analyzed to evaluate the effectiveness of this method. Bifenthrin was detected in all of sediment samples (highest concentration 260.33±41.71 μg kg⁻¹, lowest concentration 5.68±0.38 μg kg⁻¹, and fipronil sulfone was detected at least once in sediment samples collected from three sites with concentrations ranging from 1.73±0.53 to 7.53±0.01 μg kg⁻¹.
一种快速超声波提取方法与加热铜净化程序相结合,用于去除干扰成分,从而开发出一种用于分析沉积物中拟除虫菊酯和苯并吡唑类农药的方法。将 60 毫升提取物与 12 克铜粒在 60°C 下孵育 2 小时被确定为去除干扰成分的最佳条件。将 11 种拟除虫菊酯和苯并吡唑类农药加入沉积物样品中,以确定超声提取方法的有效性。在 4°C 下储存 0、1、7、14 和 21 天的沉积物中拟除虫菊酯和苯并吡唑的平均回收率范围为 98.6%至 120.0%、79.2%至 116.0%、85.0%至 119.7%、93.6%至 118.7%和 92.1%至 118.2%,所有相对标准偏差均小于 10%(大多数<6%)。这说明了在 4°C 下沉积物老化过程中拟除虫菊酯和苯并吡唑在沉积物中的稳定性。在最低添加水平(2-16 μg kg⁻¹)下,农药回收率范围为 98.6%至 120.0%,在中间添加水平(10-80 μg kg⁻¹)下,回收率范围为 97.8%至 117.9%,在最高添加水平(20-160 μg kg⁻¹)下,回收率范围为 94.3%至 118.1%。农药回收率的相对标准偏差通常小于 7%。目标农药的方法检测限范围为 0.22 μg kg⁻¹至 3.72 μg kg⁻¹。此外,还分析了在三个月监测期间从四个住宅湖泊采集的现场沉积物样品,以评估该方法的有效性。在所有沉积物样品中均检测到联苯菊酯(最高浓度为 260.33±41.71 μg kg⁻¹,最低浓度为 5.68±0.38 μg kg⁻¹,并且在至少 3 个采样点采集的沉积物样品中至少检测到一次氟虫腈砜,浓度范围为 1.73±0.53 至 7.53±0.01 μg kg⁻¹。