分析仪器
分析儀器
분석의기
ANALYTICAL INSTRUMENTATION
2013年
5期
42-49
,共8页
洪陵成%朱金伟%张红艳%刘超%马小茹
洪陵成%硃金偉%張紅豔%劉超%馬小茹
홍릉성%주금위%장홍염%류초%마소여
纳米材料%前处理%预镀汞膜%阳极溶出伏安法%铅%水质监测
納米材料%前處理%預鍍汞膜%暘極溶齣伏安法%鉛%水質鑑測
납미재료%전처리%예도홍막%양겁용출복안법%연%수질감측
nanofibers%pre-treatment%pre-coated mercury film%anodic stripping voltammetry%lead%water quality monitoring
首先,构建了基于聚苯乙烯-双硫腙纳米纤维的铅离子富集前处理装置,可以有效地降低铅的检出限并提高检测灵敏度和选择性。其次,研发了水质铅自动在线分析监测仪,以预镀汞膜的玻碳电极为工作电极,采用阳极溶出伏安法,对实验参数进行了优化,例如预镀汞膜的条件、缓冲液的种类和浓度、铅富集时间和电压等。在最优化条件下,铅的溶出峰面积与其浓度在0~2000μg/L 范围内呈现良好的线性关系,其回归方程为 y1=-0.07843+0.00269 x (相关系数为0.998,浓度范围为5~2000μg/L ),y2=-0.0035+0.00178 x (相关系数为0.998,浓度范围为5~100μg/L ),检出限为0.38μg/L。在此基础上,采用标准加入法对水样中铅的含量进行了测定,并与原子吸收法的测定结果进行了比较。结果显示,该水质铅自动在线监测仪具有快速、准确、简便、灵敏等优点。
首先,構建瞭基于聚苯乙烯-雙硫腙納米纖維的鉛離子富集前處理裝置,可以有效地降低鉛的檢齣限併提高檢測靈敏度和選擇性。其次,研髮瞭水質鉛自動在線分析鑑測儀,以預鍍汞膜的玻碳電極為工作電極,採用暘極溶齣伏安法,對實驗參數進行瞭優化,例如預鍍汞膜的條件、緩遲液的種類和濃度、鉛富集時間和電壓等。在最優化條件下,鉛的溶齣峰麵積與其濃度在0~2000μg/L 範圍內呈現良好的線性關繫,其迴歸方程為 y1=-0.07843+0.00269 x (相關繫數為0.998,濃度範圍為5~2000μg/L ),y2=-0.0035+0.00178 x (相關繫數為0.998,濃度範圍為5~100μg/L ),檢齣限為0.38μg/L。在此基礎上,採用標準加入法對水樣中鉛的含量進行瞭測定,併與原子吸收法的測定結果進行瞭比較。結果顯示,該水質鉛自動在線鑑測儀具有快速、準確、簡便、靈敏等優點。
수선,구건료기우취분을희-쌍류종납미섬유적연리자부집전처리장치,가이유효지강저연적검출한병제고검측령민도화선택성。기차,연발료수질연자동재선분석감측의,이예도홍막적파탄전겁위공작전겁,채용양겁용출복안법,대실험삼수진행료우화,례여예도홍막적조건、완충액적충류화농도、연부집시간화전압등。재최우화조건하,연적용출봉면적여기농도재0~2000μg/L 범위내정현량호적선성관계,기회귀방정위 y1=-0.07843+0.00269 x (상관계수위0.998,농도범위위5~2000μg/L ),y2=-0.0035+0.00178 x (상관계수위0.998,농도범위위5~100μg/L ),검출한위0.38μg/L。재차기출상,채용표준가입법대수양중연적함량진행료측정,병여원자흡수법적측정결과진행료비교。결과현시,해수질연자동재선감측의구유쾌속、준학、간편、령민등우점。
First ,the pre-treatment device based on polystyrene-dithizone nanofibers for lead enrich-ment was constructed ,which could reduce detection limit and improve sensitivity and selectivity effective-ly. Next ,with glassy carbon electrode pre-coated by mercury film as working electrode ,an automatic on-line analysis monitor of lead was developed by anodic stripping voltammetry ,and various experimental conditions were investigated ,i.e. ,the condition of pre-coated mercury film ,the kind and concentration of buffer solutions ,the enrichment time and voltage of lead etc.Under the optimized conditions ,the stripping peak area of lead showed a good linearity of wide range between 0-2000 μg/L. The linear regression equa-tion was y1 = -0.07843+0.00269x(R=0.998 ,with the wide range between 5-2000 μg/L) ,y2 = -0.0035+0.00178 x(R=0.998 ,with the wide range between 5-100 μg/L) ,LOD (limit of detection) = 0.38 μg/L (at a signal-to-noise ratio of 3). Then ,the water samples were determined by standard addition method.Comparing with atomic absorption spectrometry method ,this automatic on-line analysis monitor of lead was advantageous of fast ,accurate ,simple ,sensitive and cheap etc.