色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2014年
7期
717-722
,共6页
巩佳第%曹晓林%曹赵云%卞英芳%于莎莎%陈铭学
鞏佳第%曹曉林%曹趙雲%卞英芳%于莎莎%陳銘學
공가제%조효림%조조운%변영방%우사사%진명학
石墨消解%液相色谱%电感耦合等离子体质谱%砷形态%稻米%硝酸
石墨消解%液相色譜%電感耦閤等離子體質譜%砷形態%稻米%硝痠
석묵소해%액상색보%전감우합등리자체질보%신형태%도미%초산
graphite digestion%liquid chromatography( LC)%inductively coupled plasma-mass spectrometry( ICP-MS)%arsenic species%rice%nitric acid
建立了稻米中砷酸根[As(V)]、亚砷酸根[As(Ⅲ)]、砷甜菜碱(AsB)、一甲基砷(MMA)和二甲基砷(DMA)的液相色谱-电感耦合等离子体质谱( LC-ICP-MS)检测方法。以0.3 mol/L硝酸水溶液为提取试剂,样品在石墨消解仪中于95℃消解1.5 h,上清液供 LC-ICP-MS分析。5种砷形态采用 Dionex IonPac AS19阴离子交换柱(250 mm×4 mm)分离,经 ICP-MS检测。比较了4种提取液对稻米中5种砷形态的提取效率,并对提取溶剂的浓度、提取温度和提取时间等条件进行了优化。通过加标回收试验结合测定标准物质考察了方法准确度及精密度,在2个加标水平上各形态的回收率为89.6%~99.5%,RSD( n=5)不大于3.6%,大米标准物质中各形态之和的测定结果与其标准值吻合,5种砷形态的线性范围 AsB和 DMA为0.05~200μg/L,As(Ⅲ)和MMA为0.10~400μg/L,As ( V)为0.15~600μg/L,方法检出限为0.15~0.45μg/kg。结果表明,本方法简单、灵敏、耐用,可用于稻米中5种砷形态的准确定量和风险评估。
建立瞭稻米中砷痠根[As(V)]、亞砷痠根[As(Ⅲ)]、砷甜菜堿(AsB)、一甲基砷(MMA)和二甲基砷(DMA)的液相色譜-電感耦閤等離子體質譜( LC-ICP-MS)檢測方法。以0.3 mol/L硝痠水溶液為提取試劑,樣品在石墨消解儀中于95℃消解1.5 h,上清液供 LC-ICP-MS分析。5種砷形態採用 Dionex IonPac AS19陰離子交換柱(250 mm×4 mm)分離,經 ICP-MS檢測。比較瞭4種提取液對稻米中5種砷形態的提取效率,併對提取溶劑的濃度、提取溫度和提取時間等條件進行瞭優化。通過加標迴收試驗結閤測定標準物質攷察瞭方法準確度及精密度,在2箇加標水平上各形態的迴收率為89.6%~99.5%,RSD( n=5)不大于3.6%,大米標準物質中各形態之和的測定結果與其標準值吻閤,5種砷形態的線性範圍 AsB和 DMA為0.05~200μg/L,As(Ⅲ)和MMA為0.10~400μg/L,As ( V)為0.15~600μg/L,方法檢齣限為0.15~0.45μg/kg。結果錶明,本方法簡單、靈敏、耐用,可用于稻米中5種砷形態的準確定量和風險評估。
건립료도미중신산근[As(V)]、아신산근[As(Ⅲ)]、신첨채감(AsB)、일갑기신(MMA)화이갑기신(DMA)적액상색보-전감우합등리자체질보( LC-ICP-MS)검측방법。이0.3 mol/L초산수용액위제취시제,양품재석묵소해의중우95℃소해1.5 h,상청액공 LC-ICP-MS분석。5충신형태채용 Dionex IonPac AS19음리자교환주(250 mm×4 mm)분리,경 ICP-MS검측。비교료4충제취액대도미중5충신형태적제취효솔,병대제취용제적농도、제취온도화제취시간등조건진행료우화。통과가표회수시험결합측정표준물질고찰료방법준학도급정밀도,재2개가표수평상각형태적회수솔위89.6%~99.5%,RSD( n=5)불대우3.6%,대미표준물질중각형태지화적측정결과여기표준치문합,5충신형태적선성범위 AsB화 DMA위0.05~200μg/L,As(Ⅲ)화MMA위0.10~400μg/L,As ( V)위0.15~600μg/L,방법검출한위0.15~0.45μg/kg。결과표명,본방법간단、령민、내용,가용우도미중5충신형태적준학정량화풍험평고。
A method was developed for the simultaneous determination of arsenic acid[ As ( V)],arsenious acid[ As(Ⅲ)],arsenobetaine( AsB),monomethylarsonic acid( MMA)and dimethylarsinic acid( DMA)in rice by liquid chromatography-inductively coupled plasma-mass spectrometry( LC-ICP-MS). The extraction reagent was 0. 3 mol/L nitric acid with heat-assis-tant condition for 1. 5 h at 95 ℃. Then,the five arsenic species were separated by an anion exchange column(Dionex IonPac AS19,250 mm×4 mm)and detected by ICP-MS. Four kinds of extracted solutions were compared through the extraction efficiency. The concentration of nitric acid,the temperature and the extraction time were optimized. The recoveries of the five arsenic species spiked in rice at two levels ranged from 89. 6% to 99. 5% with the relative stand-ard deviations(RSDs,n=5)of 0. 6%-3. 6%. The measured values of the arsenic species in standard rice materials were consistent with their standard values. The linear ranges were 0. 05-200 μg/L for AsB and DMA,0. 10-400 μg/L for As(Ⅲ)and MMA,0. 15-600 μg/L for As ( V). The limits of detection for the five arsenic species were 0. 15-0. 45 μg/kg. The results showed that the method is much more precise for the risk assessment of the rice. This method is simple,accurate and durable for the determination of arsenic species in rice.