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Determination of glufosinate-ammonium and malathion in residue oil from palm pressed fiber using high performance liquid chromatography

机译:高效液相色谱法测定棕榈压榨纤维渣油中的草铵膦和马拉硫磷

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摘要

A study on the determination of organophosphorus pesticides (OPPs), namely glufosinate-ammonium and malathion in residue from palm pressed fiber (PPF). udThree PPF samples were taken from three different areas, FELDA Lepar, FELDA Chini 1 and FELDA Chini 2.The extraction of oil residue in PPF was carried out using supercritical fluid extraction (SFE), using supercritical carbon dioxide (CO2) at 3000 psi in isothermal in 60°C for 60 minutes. Residue then were diluted uisng acetonitrile. Chromatogram of peak analyte was determine using Waters Alliance high performance liquid chromatography (HPLC) Dissolution System Series liquid chromatography interfaced to a 2998 Photodiode Array Detector. Determination was first done using standard malathion and glufosinate-ammonium of 10, 15 and 20 ppm run on a iscoratic elution mode for 30 minutes. Optimization method later was done using water and acetonitrile as mobile phase and run for 16 minutes for malathion and 20 minutes for glufosinate-ammonium. Malathion peak is retained at 8.0 minutes while glufosinate-ammonium at 16.0 minutes. Calibration curve of the standards were plot with R 2 values of 0.9085 for malathion and 0.9249 for glufosinate-ammonium. The detection limits (LOD) were 10.3 mg/L for malathion and 14.1 mg/L for glufosinate-ammonium. Later, determination of malathion and glufosinate-ammonium were done on real samples. For malathion determination, sample from Lepar showed to have concentraion of 19.46 ppm, Chini 1 (14.34 ppm) and Chini 2 (9.72 ppm). Determination of glufosinate-ammonium showed sample from Lepar to have concentraiton of 12.64 ppm, Chini 1 (17.72 ppm) and Chini 2 (39.64 ppm).
机译:棕榈压榨纤维(PPF)残留物中有机磷农药(OPPs)(草铵膦-铵盐和马拉硫磷)的测定的研究。 ud从三个不同的区域(FELDA Lepar,FELDA Chini 1和FELDA Chini 2)采集了三个PPF样品。使用超临界流体萃取(SFE)和3000 psi的超临界二氧化碳(CO2)萃取了PPF中的残油在60°C等温下放置60分钟。然后将残余物用乙腈稀释。使用与2998光电二极管阵列检测器连接的Waters Alliance高效液相色谱(HPLC)溶解系统系列液相色谱法测定峰分析物的色谱图。首先使用标准马拉硫磷和草甘膦铵盐(分别为10、15和20 ppm)在等皮质洗脱模式下运行30分钟进行测定。随后,以水和乙腈为流动相,进行了最优化方法,马拉硫磷运行16分钟,草铵膦铵运行20分钟。马拉硫磷峰保留在8.0分钟,而草铵膦铵盐保留在16.0分钟。标出标准品的校准曲线,马拉硫磷的R 2值为0.9085,草铵膦的R 2值为0.9249。马拉硫磷的检出限(LOD)为10.3 mg / L,草铵膦-铵的检出限为14.1 mg / L。之后,对真实样品进行了马拉硫磷和草铵膦的测定。对于马拉硫磷测定,来自Lepar的样品显示其浓度为19.46 ppm,奇尼1(14.34 ppm)和奇尼2(9.72 ppm)。草铵膦铵盐的测定表明,来自Lepar的样品具有12.64 ppm,Chini 1(17.72 ppm)和chini 2(39.64 ppm)的苯乙酮。

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    Muhammad Haziq Russli;

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  • 年度 2012
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