分析试验室
分析試驗室
분석시험실
ANALYTICAL LABORATORY
2010年
4期
30-32
,共3页
何家洪%徐强%凌立新%宋仲容
何傢洪%徐彊%凌立新%宋仲容
하가홍%서강%릉립신%송중용
催化荧光法%吖啶红%痕量钴(Ⅱ)%KIO_3
催化熒光法%吖啶紅%痕量鈷(Ⅱ)%KIO_3
최화형광법%아정홍%흔량고(Ⅱ)%KIO_3
Catalysis-fluorescence%Acridine red%Trace cobalt(Ⅱ)%Potassium iodinate
在H_2SO_4介质中,KIO_3可氧化吖啶红使之褪色并伴随着吖啶红荧光强度的减弱,但其反应速率较慢.当加入痕量钴(Ⅱ)时,氧化反应明显加快,体系荧光猝灭程度加强,钴(Ⅱ)对该氧化反应具有显著的催化作用.据此建立了一种灵敏度高、选择性好的测定痕量钴(Ⅱ)的催化荧光分析新方法,并研究了该方法的动力学条件.反应体系的激发波长和发射波长分别为530和550 nm,催化体系可允许较大量的多种常见离子同时存在.测定钴(Ⅱ)的线性范围为0.3~4.8 μg/L,检出限为2.5×10~(-11)g/mL.方法可用于茶叶、人发和面粉等实际样品中痕量钴(Ⅱ)的测定.
在H_2SO_4介質中,KIO_3可氧化吖啶紅使之褪色併伴隨著吖啶紅熒光彊度的減弱,但其反應速率較慢.噹加入痕量鈷(Ⅱ)時,氧化反應明顯加快,體繫熒光猝滅程度加彊,鈷(Ⅱ)對該氧化反應具有顯著的催化作用.據此建立瞭一種靈敏度高、選擇性好的測定痕量鈷(Ⅱ)的催化熒光分析新方法,併研究瞭該方法的動力學條件.反應體繫的激髮波長和髮射波長分彆為530和550 nm,催化體繫可允許較大量的多種常見離子同時存在.測定鈷(Ⅱ)的線性範圍為0.3~4.8 μg/L,檢齣限為2.5×10~(-11)g/mL.方法可用于茶葉、人髮和麵粉等實際樣品中痕量鈷(Ⅱ)的測定.
재H_2SO_4개질중,KIO_3가양화아정홍사지퇴색병반수착아정홍형광강도적감약,단기반응속솔교만.당가입흔량고(Ⅱ)시,양화반응명현가쾌,체계형광졸멸정도가강,고(Ⅱ)대해양화반응구유현저적최화작용.거차건립료일충령민도고、선택성호적측정흔량고(Ⅱ)적최화형광분석신방법,병연구료해방법적동역학조건.반응체계적격발파장화발사파장분별위530화550 nm,최화체계가윤허교대량적다충상견리자동시존재.측정고(Ⅱ)적선성범위위0.3~4.8 μg/L,검출한위2.5×10~(-11)g/mL.방법가용우다협、인발화면분등실제양품중흔량고(Ⅱ)적측정.
Acridine red can be oxidized by potassium iodinate in dilute sulfuric acid medium with discoloring and fluorescence quenching, but the reaction rate is very low. The presence of trace cobalt(Ⅱ) can accelerate the reaction rate apparently and make the net fluorescence value of the system decrease greatly, which indicates that the trace cobalt(Ⅱ) play a role as a catalyst in this reaction remarkably. Based on the investigation above, a highly sensitive and selective catalysis-fluorescence determination method of trace cobalt(Ⅱ) has been originally proposed. The wave-length of excitation is 530 nm and the wave-length of emission is 550 nm. The method permits the existence of more than 20 common foreign ions. The linear range of concentration of cobalt is 0.3~4.8 μg/L and the limit of detection is 2.5×10~(-11)g/mL. This method has been used for the determination of trace cobalt in tea, hair and wheat flour samples with satisfactory results.