摘要
研究并建立了醚磺隆(cinosulfuron)在水稻植株、稻米、土壤及田水中的残留分析方法。水稻植株和稻米样品以甲醇提取,经石油醚、二氯甲烷液液分配,固相萃取(SPE)净化,高效液相色谱(HPLC)测定;土壤样品经甲醇提取后,高效液相色谱(HPLC)测定;田水样品经固相萃取(SPE)净化,高效液相色谱(HPLC)测定。醚磺隆的最小检测量为2ng,水稻植株和稻米中醚磺隆最小检测浓度为0.04mg·kg^-1;土壤中醚磺隆最小检测浓度为0.02mg·kg^-1;田水中醚磺隆的最小检测浓度为0.04mg·L^-1。添加浓度0.04—0.2mg·kg^-1时,水稻植株中醚磺隆的回收率为98.1%~105.9%,变异系数3.9%-4.4%;稻米中醚磺隆的回收率为87.8%~98.8%,变异系数2.9%~6.6%;添加浓度0.02~0.2mg·kg^-1时,土壤中醚磺隆的回收率为87.9%~100.5%,变异系数2.5%~7.3%;添加浓度0.04~0.2mg·L^-1时,田水中醚磺隆的回收率为86.2%~107.9%,变异系数为3.3%~8.6%。该方法的准确性、精确性以及灵敏度均符合农药残留分析的要求。
SPE-HPLC was used to analyse residue of cinosulfuron in rice plant , rice, soil and water. Residues of cinosulfuron were extracted from rice plant , rice and soil with methanol, cleaned up by SPE cartridge, and determined by HPLC equipped with UV detector. The average recoveries and coefficients of variation of the method were 98.09% ~105.96% ,3.99% ~4.36% for rice plant samples;87.76% ~98.75% ,2.88%~6. 75% for rice samples; 87.85% ~ 100. 53% ,2.45% ~7.26% for soil samples; 86. 19% ~ 107.90% ,3.31% ~8.59% for water samples, respectively. The minimum detectable amount of cinosulfuron was 2ng, and the minimum detectable concentrations was 0. 04,0.02 mg· kg^-1 and 0. 04 mg·L^-1,respectively. The results showed that the method meet with demands of pesticide residue analysis.
出处
《安徽农业大学学报》
CAS
CSCD
北大核心
2010年第1期88-92,共5页
Journal of Anhui Agricultural University
基金
国家"十一五"科技支撑计划项目(2006BAK02A0403
2007BAD87B06)
安徽省学术带头人基金
安徽省"十一五"科技攻关项目(08010302166)共同资助