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1.
氢化物发生-原子荧光光谱法测定中草药中的痕量铋   总被引:3,自引:1,他引:3  
本文报道了采用氢化物-原子荧光法测定中草药中的痕量铋。试验了酸介质和还原剂用量对测定铋的影响,考察了共存金属离子的干扰。在最佳测定条件下,方法检出限为0.1μg/L,线性范围为0.1~200μg/L,加标回收率为91.0%~104.2%。  相似文献   

2.
《Analytical letters》2012,45(6):1609-1622
Abstract

A sensitive determination of bismuth by hydride generation with non-dispersive atomic fluorescence spectrometric detection is proposed. A commercially available electrodeless discharge lamp was used as the light source. Studies on interference effects from foreign elements are reported and the determination of bismuth in copper metal was considered in detail.  相似文献   

3.
《Analytical letters》2012,45(17):2623-2636
Experimental variables in continuous flow hydride generation inductively coupled plasma-optical emission spectrometry (CF-HG-ICP-OES) were optimized for determination of bismuth. Concentrations of NaBH4, HCl, and NaOH, flow rates of NaBH4, sample solution, waste and carrier argon, radio frequency power, lengths of reaction, and stripping coils were optimized to obtain lower detection limits. Under optimum conditions, the detection limit was calculated as 0.16 ng mL?1, and the calibration plot was linear between 1.0–50.0 ng mL?1. An improvement in detection limit of 5.75 times by CF-HG-ICP-OES was reached vs. ICP-OES. Relative standard deviation (RSD) for ten replicate measurements of 10.0 ng mL?1 Bi was calculated as 3.9%. Effect of possible interferic ions on Bi signal was evaluated. Accuracy of method was verified by using a standard reference material, SRM 1643e. Results found for Bi were in satisfactory agreement with certified values. The proposed method was then employed to determine trace concentration of Bi in milk samples. Bi amounts in samples were found in the range from lower than the quantitation limit to 14.5 ng mL?1, whereas Bi concentrations were lower than the detection limit in three samples.  相似文献   

4.
对CCl4/Ar混合气体脉冲直流高压放电产生CCl2自由基,在超声射流冷却下获得了CCl2 1B1- 1A1420~600 nm 波长范围的激光诱导荧光激发谱,系统标识了9个带系,81个振动带,其中56个振动带是我们新标识的.通过CCl2自由基的超声射流LIF谱与常温下压力为150 Pa 左右的LIF谱相结合分析,初步证实CCl2自由基电子态带源为17 255.04 cm-1.  相似文献   

5.
HG-AFS 法测定多金属矿中的痕量锡   总被引:5,自引:0,他引:5  
研究了酒石酸介质中氢化物发生原子荧光光谱法 ( HG- AFS)测定多金属矿中痕量锡的方法 ,考察了不同酸介质和浓度对氢化物发生效率的影响 ,试验了共存元素的干扰情况。方法的检出限为 1 .4× 1 0 - 10 g/ m L,精密度 ( n=5)为3.71 %~ 5.38%。  相似文献   

6.
氢化物—原子荧光光光谱法同时测定黄铜中的砷与锑   总被引:4,自引:1,他引:4  
试样用硝酸-硫酸分解,试验了酸度、还原剂浓度以及黄铜中常见元素对测定结果的影响,砷、锑的回收率分别为:96%~109%,90%~93%,砷、1锑的检出限分别为0.19ng=mL、0.31ng=mL,砷、锑的线性范围分别为0.5~250ng/mL、0.5~500ng/mL。本法用于黄铜标准样品中的砷、锑。结果与标准值吻合。  相似文献   

7.
High resolution laser induced fluorescence, spectra of IrN in the spectral region between 394 and 520 nm were recorded using laser vaporization/reaction free jet expansion and laser induced fluorescence spectroscopy. Seven new vibronic transition bands were observed and analyzed. Two Ω=1 and five Ω=0 new states were identified. Least squares fit of rotationally resolved transition lines yielded accurate molecular constants for the upper states. Spectra of isotopic molecules were observed, which provided confirmation for the vibrational assignment. Comparison of the observed electronic states of IrB, IrC, and IrN provides a good understanding of the chemical bonding of this group of molecules.  相似文献   

8.
氢化物发生-原子荧光光谱法(HG-AFS)是测定土壤样品中硒(Se)的理想方法,常用SePb合金材质的空心阴极灯为激发光源,无色散系统的AFS测硒时存在铅的光谱干扰,但尚未引起广泛关注。本文研究了高浓度Pb对硒测定的影响,并提出一种干扰校正的方法,可对检测结果进行有效校正。同时对还原剂浓度和消解酸的比例进行了优化,在2~40 ng/mL范围内获得Se标准曲线r2=0.9989,检出限为0.0023 ug/g,方法精密度为2.9-9.8%,准确度ΔlogC小于0.035。对南疆铁门关区域地球化学调查样品进行了测定,校正后Se的检测结果合格率为94.0%。此方法具有操作简单、准确高效,能够有效的校正样品中高浓度Pb的干扰,适合于大批量区域地球化学调查样品的检测。  相似文献   

9.
《Analytical letters》2012,45(8):894-906
Studies have been performed to evaluate a direct laser induced fluorescence (LIF) technique for measurements of atmospheric sulfur dioxide (SO2). The technique is novel in that it uses a nontunable laser source that is spectrally coincident with absorption of the SO2 molecule near 223 nm that allows sensitive measurements at environmentally relevant concentrations. In this report, the spectral characteristics and analytical capabilities of the nontunable LIF approach have been evaluated and preliminary measurements of ambient SO2 are reported. The current limit of detection is 0.5 ppb and compares well to other analytical spectroscopy methods used for atmospheric measurements of SO2. The results indicate strong feasibility for the nontunable LIF approach for SO2 measurements and suggest ways for method improvement.  相似文献   

10.
对微流控芯片检测技术的研究一直是近年来微全分析系统领域的研究热点.激光诱导荧光(Laser induced fluorescence,LIF)检测技术因其具有较高的灵敏度,成为目前微流控分析芯片采用最广的检测方法[1].  相似文献   

11.
《Analytical letters》2012,45(14):2006-2013
A simple, sensitive, and interference free method was proposed for the determination of total arsenic in high purity indium oxide by hydride generation atomic fluorescence spectrometry (HG-AFS). Preconcentration was carried out by distillation of volatile arsenic trichloride. Hydrazine sulfate was used as a prereductant to reduce As (V) to As (III). The volatile arsenic trichloride generation was based on the reaction between As (III) and hydrochloric acid, and vapors were absorbed with water. The method provides a linear response range of 2 ng/mL–70 ng/mL, a detection limit of 0.1 ng/mL, a recovery of 96%–113%, and an average relative standard deviation of 2.42%. The method was validated by means of interlaboratory comparative analysis with the proposed method HG-AFS, and the comparison of data by using proposed method HG-AFS and reference methods of ICP-OES and spectrophotometry.  相似文献   

12.
本文将电热氢化物原子吸收光谱技术应用于食品中微量锑铋测定,检出限可达ppb级。探讨了被测元素价态、预还原条件等因素对测定灵敏度的影响,并应用于罐头食品中微量锑铋分析。  相似文献   

13.
氢化物发生新体系-原子荧光法同时测定铅和镉   总被引:1,自引:0,他引:1  
报道了Pb和Cd同时氢化物发生的K3Fe(CN)6-(NH4)2Ce(NO3)6-NaBH4-HCl新体系,并探讨了相关反应机理。(NH4)2Ce(NO3)6作为氧化剂将Pb(Ⅱ)氧化为Pb(Ⅳ),Fe(CN)63-与Pb(Ⅳ)络合促进了Pb的氢化物发生。同时,体系中的(NH4)2Ce(NO3)6作为Cd氢化物发生过程中的增敏剂使荧光信号显著增强。在该体系中,Pb和Cd的氢化物发生不产生相互干扰。本实验据此建立了顺序注射-氢化物发生-双道原子荧光同时测定Pb和Cd的方法。所采用的实验条件包括NaBH4、HCl、K3Fe(CN)6和(NH4)2Ce(NO3)6的浓度分别为2%、3%、0.6%和0.3%。以125μL/s进样500μL,得到的线性范围分别为0.4~15μg/L(Pb)和0.5~20μg/L(Cd);对应的检出限分别为0.09μg/L(Pb)和0.17μg/L(Cd);方法的精密度为0.5%(6.0μg/L Pb,n=9)和1.0%(6.0μg/L Cd,n=9)。将本法应用于国家标准样品GBW08608中Pb和Cd的检测,检测值与标准值相符;对河水及海水中Pb和Cd进行了同时测定,加标回收率合格。  相似文献   

14.
流动注射氢化物发生原子荧光法测定中药中的微量As、Hg   总被引:33,自引:0,他引:33  
建立了一套流动注射-氢化物发生-原子荧光测定中药样品中微量As、Hg的方法,研究了酸度、NaBH4浓度、载气流速等条件对检出限的影响.在优化的工作条件下,对砷、汞的检出限分别为0.1ng/mL和0.02ng/mL.本法具有操作简便、快速,灵敏度高等优点,可用于中药样品中微量As、Hg的测定.  相似文献   

15.
碱式模式氢化物发生原子荧光法测定食用菌中痕量锗   总被引:8,自引:3,他引:8  
研究了碱式模式氢化物发生原子荧光法测定痕量锗。考察了HG-AFS仪器参数及氢化物发生条件对锗荧光强度的影响以及常见共存元素的干扰。在选定的最佳工作条件下,测定了真菌中的痕量锗。方法检出限(3σ)为0.76μg/L,相对标准偏差(RSD)为0.81%,回收率为94.6%-101.3%。  相似文献   

16.
氢化物原子荧光光谱法测定虾中砷和汞   总被引:1,自引:0,他引:1  
建立了氢化物原子荧光法同时测定虾中砷和汞的方法。研究了样品前处理及实验条件对测定砷、汞的原子荧光强度的影响,并探讨了共存离子对测定砷、汞的干扰和消除的方法。本方法具有操作简便、快速、灵敏度高等优点,砷和汞的检出限分别为0.026μg/L和0.020μg/L;相对标准偏差分别为1.7%~9.4%和1.2%~9.4%;回收率为98%~106%。  相似文献   

17.
本文提出用乙醇作为 NaBH_4的溶剂,APDC-MIBK 有机相氢化物发生原子荧光光谱法测定饮用水中砷。与 DMF 相比,乙醇溶剂具有价廉、无毒性以及荧光背景小,可以在较低酸度下发生氢化物的特点。对非水介质氢化物发生法的推广应用具有较大的实用价值。  相似文献   

18.
曾焕济  黄俐俐 《分析化学》2000,10(3):381-384
研制半自动定容试液,半自动定位恒速注入KBK4,整个氢化过程不串空气,可用压力全方位喷射冲洗反应室。该装置定容定位准确,操作简便快速,适用于大批量样品分析。通过对8个GSD标准参考物质的分析,分析结果与参考值基本一致,RSD<6%。  相似文献   

19.
Proteomics is becoming more and more mature,but the detection of low abundance proteins is still a difficult task.Laser-induced fluorescence(LIF) detection is one of the most sensitive detection methods in a capillary electrophoresis(CE)system[1-3].However,most proteins do not exhibit favourable native fluorescence,a derivatization procedure is necessary for LIF detection of proteins.Since the derivatization reaction between protein and fluorescent reagent takes place after the separation of protein,the separation cannot be compromised by multiple derivatization products,the post-column derivatization becomes an attractive method for derivatization in CE-LIF system[4'5].The gap reactor,coaxial reactor and sheath flow cuvette reactor have been widely used for post-column derivatization in CE-LIF system[6].The gap reactor is constructed by aligning separation and reaction capillaries with a small gap[7,8].  相似文献   

20.
建立了流动注射氢化物发生非色散原子荧光光谱法测定中药成药中微量As和Pb的方法 ;研究了酸度、载气流速、KBH4 浓度及流速等条件对荧光信号强度的影响 ;优化实验条件下 ,方法对As和Pb的检出限分别为0.016和0.42μg·L-1 ,相对标准偏差分别为1.1 %和0.48 % (As75.7μg·L-1 ,Pb100μg·L-1 ,n=12) ;方法具有操作简便、快速、灵敏度高的优点 ,可用于中药成药中微量As和Pb的测定。  相似文献   

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