分析化学
分析化學
분석화학
CHINESE JOURNAL OF ANALYTICAL CHEMISTRY
2001年
5期
546-548
,共3页
陈兴国%胡之德%许红平%李江
陳興國%鬍之德%許紅平%李江
진흥국%호지덕%허홍평%리강
锇(Ⅳ),偶氮氯膦-mA,催化光度法,正交实验设计
鋨(Ⅳ),偶氮氯膦-mA,催化光度法,正交實驗設計
철(Ⅳ),우담록련-mA,최화광도법,정교실험설계
在碱性介质中,锇(Ⅳ)对KIO4氧化偶氮氯膦-mA的褪色反应有明显的催化作用,据此建立了催化光度法测定微量锇(Ⅳ)的新方法,并用正交实验设计对反应条件进行了优化。方法的检测限为2.0μg/L。锇(Ⅳ)含量在7.0~25.0μg/L范围内服从比尔定律。此方法已用于贵金属精矿和二次合金中微量锇的测定,相对误差均为0.9%,回收率在95.38%~106.0%之间。
在堿性介質中,鋨(Ⅳ)對KIO4氧化偶氮氯膦-mA的褪色反應有明顯的催化作用,據此建立瞭催化光度法測定微量鋨(Ⅳ)的新方法,併用正交實驗設計對反應條件進行瞭優化。方法的檢測限為2.0μg/L。鋨(Ⅳ)含量在7.0~25.0μg/L範圍內服從比爾定律。此方法已用于貴金屬精礦和二次閤金中微量鋨的測定,相對誤差均為0.9%,迴收率在95.38%~106.0%之間。
재감성개질중,철(Ⅳ)대KIO4양화우담록련-mA적퇴색반응유명현적최화작용,거차건립료최화광도법측정미량철(Ⅳ)적신방법,병용정교실험설계대반응조건진행료우화。방법적검측한위2.0μg/L。철(Ⅳ)함량재7.0~25.0μg/L범위내복종비이정률。차방법이용우귀금속정광화이차합금중미량철적측정,상대오차균위0.9%,회수솔재95.38%~106.0%지간。
A catalytic spectrophotometric method for the determination of micro amounts of osmium has been established based on the catalytic action of Os(Ⅳ) on the oxidation fading reaction of chlorophosphonazo-mA with KIO4 in alkaline-medium. The reaction conditions were optimized by orthogonal experimental design. The detection limit for osmium was 2.0 μg/L.Beer's law was obeyed in the range from 7.0 to 25.0 μg/L for Os(Ⅳ). The method has been applied to the determination of micro amounts of Os(Ⅳ) in concentrate of noble metals and secondary alloy,both of the relative errors were 0.9%. Recoveries varied from 95.38% to 106.0%.