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固相萃取-高效液相色谱法测定水中痕量甲磺隆
其他题名SPE-HPLC Determination of Trace Amounts of Metsulfuron-Methyl in Water
施跃锦; 蔡美强
来源期刊理化检验. B, 化学分册
ISSN1001-4020
出版年2010
卷号46期号:8页码:923-925
中文摘要提出了高效液相色谱法测定水中痕量甲磺隆. 水样经Oasis~R MCX固相萃取小柱富集并净化后,以Extend C18柱(250 mm*4.6 mm,5mum)为固定相,0.2 mol·L~(-1)甲酸-甲醇-乙腈 (60+20+20)混合溶液为流动相进行分离,在225 nm波长处,用二极管阵列检测器测定. 甲磺隆浓度在0.005~5.0 mg·L~(-1)范围内与其峰面积呈线性关系,测定下限(10S/N)为0.005 mg· L~(-1). 方法用于水样分析,加标回收率在94.0%~102.0%之间,相对标准偏差(n=6)小于6.5%
英文摘要High performance liqiud chromatography with solid phase extraction was applied to the determination of residual amount of metsulfuron-methyl in water. The sample was enriched and purified by Oasis MCX SPE column. The eluate obtained was separated on Extend C_(18) column (250 mm*4.6 mm, 5mum), using a mixture of 0.2 mol·L~(-1)formic acid, methanol and acetonitrile mixed in the ratio of 60 to 20 to 20 (by volume) as mobile phase. DAD-detection at 225 nm was used in the determination. Linear relationship between values of peak area and mass concentration of metsulfuron-methyl was kept in the range of 0.005-5.0 mg·L~(-1). Lower limit of determination (10S/N) of the method was found to be 0.005 mg·L~(-1). On the base of water sample, test for recovery were made by standard addition method, values of recovery found were in the range of 94.0%-102.0%, and values of RSD′s (n=6)were less than 6.5%
中文关键词高效液相色谱法 ; 固相萃取 ; 甲磺隆 ; 水
英文关键词HPLC Solid phase extraction Metsulfuron-methyl Water
语种中文
国家中国
收录类别CSCD
WOS类目CHEMISTRY ANALYTICAL
WOS研究方向Chemistry
CSCD记录号CSCD:3984766
资源类型期刊论文
条目标识符http://119.78.100.177/qdio/handle/2XILL650/225359
作者单位浙江工商大学环境科学与工程学院, 浙江 310035, 中国
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GB/T 7714
施跃锦,蔡美强. 固相萃取-高效液相色谱法测定水中痕量甲磺隆[J],2010,46(8):923-925.
APA 施跃锦,&蔡美强.(2010).固相萃取-高效液相色谱法测定水中痕量甲磺隆.理化检验. B, 化学分册,46(8),923-925.
MLA 施跃锦,et al."固相萃取-高效液相色谱法测定水中痕量甲磺隆".理化检验. B, 化学分册 46.8(2010):923-925.
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