湖北民族学院学报(自然科学版)
湖北民族學院學報(自然科學版)
호북민족학원학보(자연과학판)
JOURNAL OF HUBEI INSTITUTE FOR NATIONALITIES(NATURAL SCIENCE EDITION)
2014年
1期
57-59
,共3页
刘波%付丁强%牛明明%部美玲%黄文胜
劉波%付丁彊%牛明明%部美玲%黃文勝
류파%부정강%우명명%부미령%황문성
1-(2-吡啶偶氮)-2-萘酚%化学修饰电极%汞%伏安法
1-(2-吡啶偶氮)-2-萘酚%化學脩飾電極%汞%伏安法
1-(2-필정우담)-2-내분%화학수식전겁%홍%복안법
1-( 2-pyridylazo )-2-naphthol%chemically modified electrodes%mercury%voltammetry
研究了1-(2-吡啶偶氮)-2-萘酚修饰玻碳电极检测痕量汞的电分析方法.汞离子通过与电极表面的1-(2-吡啶偶氮)-2-萘酚发生配位作用而富集在电极表面,同时在-0.80 V ( vs.SCE )还原成零价的汞,当电极电势从-0.80 V向0.00 V扫描时,被还原的汞则从电极表面溶出,于-0.18 V处出现灵敏的阳极溶出峰.优化了支持电解质及pH、1-(2-吡啶偶氮)-2-萘酚的用量、富集电位及富集时间等实验参数.利用1-(2-吡啶偶氮)-2-萘酚修饰电极测定的汞的线性范围为2.0×10-9 mol/L到9.0×10-7 mol/L,检测限为6×10-10 mol/L.此方法用于水试样中汞含量的测定,平均回收率为99.88%.
研究瞭1-(2-吡啶偶氮)-2-萘酚脩飾玻碳電極檢測痕量汞的電分析方法.汞離子通過與電極錶麵的1-(2-吡啶偶氮)-2-萘酚髮生配位作用而富集在電極錶麵,同時在-0.80 V ( vs.SCE )還原成零價的汞,噹電極電勢從-0.80 V嚮0.00 V掃描時,被還原的汞則從電極錶麵溶齣,于-0.18 V處齣現靈敏的暘極溶齣峰.優化瞭支持電解質及pH、1-(2-吡啶偶氮)-2-萘酚的用量、富集電位及富集時間等實驗參數.利用1-(2-吡啶偶氮)-2-萘酚脩飾電極測定的汞的線性範圍為2.0×10-9 mol/L到9.0×10-7 mol/L,檢測限為6×10-10 mol/L.此方法用于水試樣中汞含量的測定,平均迴收率為99.88%.
연구료1-(2-필정우담)-2-내분수식파탄전겁검측흔량홍적전분석방법.홍리자통과여전겁표면적1-(2-필정우담)-2-내분발생배위작용이부집재전겁표면,동시재-0.80 V ( vs.SCE )환원성령개적홍,당전겁전세종-0.80 V향0.00 V소묘시,피환원적홍칙종전겁표면용출,우-0.18 V처출현령민적양겁용출봉.우화료지지전해질급pH、1-(2-필정우담)-2-내분적용량、부집전위급부집시간등실험삼수.이용1-(2-필정우담)-2-내분수식전겁측정적홍적선성범위위2.0×10-9 mol/L도9.0×10-7 mol/L,검측한위6×10-10 mol/L.차방법용우수시양중홍함량적측정,평균회수솔위99.88%.
1-( 2-pyridylazo )-2-naphthol-modified glassy carbon electrode has been investigated to de-tect trace levels of Hg2+.Hg2+are preconcentrated on the surface of the 1-(2-pyridylazo) -2-naphthol-modified glassy carbon electrode at -0.80 V(vs.SCE), and subsequently reduced on the electrode .In the following step , reduced mercury is oxidized , and voltammograms are recorded by scanning the poten-tial towards a positive direction .The peak currents are linear with the concentrations in the range from 2. 0×10-9 mol/L to 9.0×10-7 mol/L for Hg2+.The detection limits are 6×10-10 mol/L for Hg2+.The coeffi-cients of variation, determined on one single electrode at a concentration of 5×10-7 mol/L Hg2+,have been calculated to be 2.8%for Hg2+(n=8).Using this kind of modified electrode, trace levels of Hg2+in several water samples are determined , and the average recovery is 99.88%.