信阳师范学院学报(自然科学版)
信暘師範學院學報(自然科學版)
신양사범학원학보(자연과학판)
JOURNAL OF XINYANG NORMAL UNIVERSITY(NATURAL SCIENCE EDITION)
2015年
2期
214-217
,共4页
曹俊涛%王辉%刘启祥%刘彦明
曹俊濤%王輝%劉啟祥%劉彥明
조준도%왕휘%류계상%류언명
流动注射%化学发光%银纳米%对苯二酚
流動註射%化學髮光%銀納米%對苯二酚
류동주사%화학발광%은납미%대분이분
flow-injection%chemiluminescence%AgNPs%hydroquinone
在碱性条件下,银纳米( AgNPs)对luminol-K3 Fe( CN)6化学发光体系具有显著的增强作用.研究发现,对苯二酚( HQ)对luminol-K3 Fe( CN)6-AgNPs化学发光体系具有抑制作用.结合流动注射技术提出了lumi-nol-K3Fe(CN)6-AgNPs化学发光(FI-CL)灵敏检测HQ的新方法.结果表明,HQ的线性范围为1.0×10-10~1.0×10-7 mol? L-1,检出限为3.0×10-11 mol ? L-1,对5.0×10-9 mol? L-1的HQ溶液平行测定11次的RSD为1.4%.将提出的方法分别用于河水和自来水中HQ 含量的测定,加标回收率分别为98.0%~100.8%和99.1%~100.4%.结合化学发光光谱,对银纳米增强luminol-K3Fe(CN)6化学发光体系以及HQ对该体系的抑制作用机理进行了探讨.
在堿性條件下,銀納米( AgNPs)對luminol-K3 Fe( CN)6化學髮光體繫具有顯著的增彊作用.研究髮現,對苯二酚( HQ)對luminol-K3 Fe( CN)6-AgNPs化學髮光體繫具有抑製作用.結閤流動註射技術提齣瞭lumi-nol-K3Fe(CN)6-AgNPs化學髮光(FI-CL)靈敏檢測HQ的新方法.結果錶明,HQ的線性範圍為1.0×10-10~1.0×10-7 mol? L-1,檢齣限為3.0×10-11 mol ? L-1,對5.0×10-9 mol? L-1的HQ溶液平行測定11次的RSD為1.4%.將提齣的方法分彆用于河水和自來水中HQ 含量的測定,加標迴收率分彆為98.0%~100.8%和99.1%~100.4%.結閤化學髮光光譜,對銀納米增彊luminol-K3Fe(CN)6化學髮光體繫以及HQ對該體繫的抑製作用機理進行瞭探討.
재감성조건하,은납미( AgNPs)대luminol-K3 Fe( CN)6화학발광체계구유현저적증강작용.연구발현,대분이분( HQ)대luminol-K3 Fe( CN)6-AgNPs화학발광체계구유억제작용.결합류동주사기술제출료lumi-nol-K3Fe(CN)6-AgNPs화학발광(FI-CL)령민검측HQ적신방법.결과표명,HQ적선성범위위1.0×10-10~1.0×10-7 mol? L-1,검출한위3.0×10-11 mol ? L-1,대5.0×10-9 mol? L-1적HQ용액평행측정11차적RSD위1.4%.장제출적방법분별용우하수화자래수중HQ 함량적측정,가표회수솔분별위98.0%~100.8%화99.1%~100.4%.결합화학발광광보,대은납미증강luminol-K3Fe(CN)6화학발광체계이급HQ대해체계적억제작용궤리진행료탐토.
Silver nanoparticles (AgNPs) exhibited better chemiluminescence (CL) catalysis activity in luminol-K3Fe(CN)6 system under alkaline condition.It was found that the CL intensity of luminol-K3Fe(CN)6-AgNPs was strongly inhibited in the presence of hydroquinone (HQ).Based on the luminol-K3Fe(CN)6-AgNPs CL system, a sensitive method to detect HQ by flow injection( FI) coupled with chemiluminescence ( CL) detection was described. Under the optimized conditions, the sensitive detection of HQ could be realized and the detection limit of HQ was cal-culated to be 3.0 ×10 -11 mol/L with a linear range of 1.0 ×10 -10 ~1.0 ×10 -7 mol/L.The relative standard devi-ation of 1.4%for 11 replicate determinations of 5.0 ×10 -9 mol/L was obtained.The method was applied to the HQ analysis of river water and tap water samples with recoveries of 98.0%~100.8%and 99.1%~100.4%, respective-ly.The possible mechanism of AgNPs enhancing effect on the weak CL emission of K3 Fe( CN) 6 system and the inhibi-tion effect of HQ on the system was discussed by fluorescence spectrophotometer.