分析试验室
分析試驗室
분석시험실
ANALYTICAL LABORATORY
2010年
3期
27-29
,共3页
欧阳辉祥%莫艳琴%蒋治良
歐暘輝祥%莫豔琴%蔣治良
구양휘상%막염금%장치량
乐果%共振散射%纳米金%磷锑钼蓝
樂果%共振散射%納米金%燐銻鉬藍
악과%공진산사%납미금%린제목람
Dimethoate%Organophosphoantimon molybdate blue%Nanogold%Resonance scattering spectral method
在H_2SO_4介质中,有机磷乐果和钼酸钠、酒石酸锑钾反应,生成淡黄色的有机磷锑钼三元杂多酸,纳米金在726 nm处产生一个较强的共振散射峰. 抗坏血酸可将该有机磷锑钼杂多酸还原为有机磷锑钼杂多蓝,导致726 nm处共振散射峰的强度降低. 乐果质量浓度在0.014~1.66 μg/mL范围内与共振散射光强度降低值ΔI呈良好的线性关系,其回归方程为ΔI=155.4ρ+1.4,相关系数为0.9970,方法的检出限为3.9 ng/mL,该法可用于废水中乐果的测定.
在H_2SO_4介質中,有機燐樂果和鉬痠鈉、酒石痠銻鉀反應,生成淡黃色的有機燐銻鉬三元雜多痠,納米金在726 nm處產生一箇較彊的共振散射峰. 抗壞血痠可將該有機燐銻鉬雜多痠還原為有機燐銻鉬雜多藍,導緻726 nm處共振散射峰的彊度降低. 樂果質量濃度在0.014~1.66 μg/mL範圍內與共振散射光彊度降低值ΔI呈良好的線性關繫,其迴歸方程為ΔI=155.4ρ+1.4,相關繫數為0.9970,方法的檢齣限為3.9 ng/mL,該法可用于廢水中樂果的測定.
재H_2SO_4개질중,유궤린악과화목산납、주석산제갑반응,생성담황색적유궤린제목삼원잡다산,납미금재726 nm처산생일개교강적공진산사봉. 항배혈산가장해유궤린제목잡다산환원위유궤린제목잡다람,도치726 nm처공진산사봉적강도강저. 악과질량농도재0.014~1.66 μg/mL범위내여공진산사광강도강저치ΔI정량호적선성관계,기회귀방정위ΔI=155.4ρ+1.4,상관계수위0.9970,방법적검출한위3.9 ng/mL,해법가용우폐수중악과적측정.
Organic phosphorus dimethoate reacted with molybdate and antimony tartrate potassium to from organophosphoantimomolybdate heteropoly acid in light yellow, and the nanogold exhibited a strong resonance scattering peak at 726 nm in 0.012 mol/L H_2SO_4. When ascorbic acid was added, the heteropoly acid was reduced to organophosphoantimomolybdate blue that resulted in the resonance scattering intensity quenching at 726 nm. The decreased intensity ΔI was linear to the concentration of dimethoate in the range of 0.014~1.66 μg/mL, with regression equation of ΔI=155.4ρ+1.4,correlation coefficient of 0.9970, and detection limit of 3.9 ng/mL. This resonance scattering method was applied to the analysis of dimethoate in waste water samples, with simplicity, rapidity and accuracy.