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作 者:李志明[1]
机构地区:[1]漳州职业技术学院食品与生物工程系,福建漳州363000
出 处:《喀什师范学院学报》2008年第6期45-48,共4页Journal of Kashgar Teachers College
基 金:福建省自然科学基金计划资助项目(项目编号:2008J0313;D0510027)
摘 要:基于Triton X-100增敏钛催化过氧化氢氧化β,β-二羟基连二萘酚(R)反应,导致R的固体基质室温磷光信号猝灭效应,建立了高灵敏度固体基质室温磷光(SS—RTP)测定痕量Ti(IV)的新方法.Ti(IV)量在0.010-2.00fg斑^-1(对应浓度范围0.025~5.0pg·mL^-1,点样体积0.40μL)与磷光信号△Ip成线性关系,回归方程△Ip=11.52+10.73CTi(IV)(pg·mL^-1)},r=0.9993,检出限0.0045fg·斑^-1(对应浓度为1.1×10^-14g.mL^-1).所建立方法成功用于茶叶、人发样品中痕量钛的测定,加标回收率分别为99.2%和103.3%,RSD分别为2.9%和3.8%.A new solid substrate-room temperature phosphorimetry for the determination of trace titanium (IV) has been established. Based on the fact that triton X - 100 can spike titanium to catalyze H2O2 oxidizing β,β' -dihydroxy-dinaphthol (R), which can cause sharp quenching of room temperature phosphorescence. The relationship between the △Ip of the emitting intensity and 0.01 --2.00 fg.spot^-1Ti(IV) (corresponding concentration: 0. 025-- 5.0 pg.mL^-1 sample volume 0.40 μL) conforms to the linearity. The regression equation of working curve can be expressed as △Ip= 11.52 + 10.73 CTi(IV) (pg. mL^- 1 ), r = 0. 9993. The limit detection (LD) is 0. 0045 fg.spot^-1 (corresponding concentration 1.1 --10^-14 g. mL^-1). This method has been successfully applied to the determination of trace titanium (IV) in real samples of tea and human hair with satisfactory results, the standard addition recoveries are 99.2 % and 103.3 %, RSD are 2.9 % and 3. 8%.
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