Transcript AnionsCE
Concentration Determination via Leucigenin Quenching and Indirect CE Christopher Hampton, Dr. Eamonn F. Healy, QuickTime™ and a Photo - JPEG decompressor are needed to see this picture. Chemistry Department, St. Edward’s University, Austin TX 78704 Background on Capillary Electrophoresis Capillary (20-200x10^-6 M inner diameter) High voltages Electroosmotic Flow Electrophoretic Flow UV Spectroscopy Benefits Minute samples (uL Samples may be used) Fast separation Linear quantization Electrophoretic/osmotic Flow Electrophoretic Flow µ=[Ld/tm]/[V/Lt] Ld = length to detector tm = migration time V = voltage Lt = total length Electroosmotic Flow Veo=[Edc(Zp)/4πn]/E Edc = dielectric constant Zp = Zeta potential n = viscosity E = electric field strength CE Experimental Method Instrument Used P/ACE 5000 CE Fused silica capillaries at 57cm x 75µm Working length 50cm 6 second pressure injections Chemicals Used All of ACS reagent grade All solutions were made with Millipore water Experimental Method, contd. BGE Composition Chromic Acid Hydroxybenzenesulfonic Acid 5 mM 5 mM Ratio of BGE’s 1:1 Buffered with diethanolamine to pKa of DEA pH 9.2 Indirect Detection Background Electrolytes (BGE) BGE1, BGE2 UV absorbing species Analytes displace electrolytes Results in “negative” peak, analytes do not absorb Negative peak flipped by software Indirect Detection Methods BGE composition Chromic Acid CAS [7738-94-5] 5mM Hydroxybenzenesulfonic Acid CAS [1333-39-7] 5mM Ratio 1:1 DEA (Diethylanolamine) CAS [111-42-2] pKa of DEA ~pH 9.2 Chromate Chromatograph, 5mM OH-BSA Chromatograph, 5mM Chloride Chromatograph, 0.2mM Fluorescence Work Lucigenin has been widely known to be quenched by Chloride anions for a long time This phenomenon has not been extensively studied, and no detailed analytical characterization has been done. Fluoroscopy Benefits Small samples (3mL) Widely available Limitations Not all materials fluoresce Cost of fluorescent materials Detection limits Fluoroscopy Experimental Method Instrument Used Shimadzu RF 5301 PC Fluorometer Suprasil 4mL Fluorescence cuvette (1cm base) Chemicals Used All of ACS reagent grade Chloride solutions were made from a volumetric NaCl standard solution obtained from Sigma Aldrich (1g Cl- / 100g water) All solutions were made with Millipore water Experimental Method, contd. Standards prepared Lucigenin concentration from an ethanol stock, diluted in water Solutions were combined in a capped cuvette, and vortexed for 30-45 seconds Experimental Method, contd. An excitation spectrum was obtained at 505nm Maximum peak intensity and differentiation was consistently observed at 368 and 432 nm 0.1 µM Lucigenin Quenching 0.1 µM Lucigenin Regression 0.05 µM Lucigenin Quenching 0.05 µM Lucigenin Regression Preliminary Results and Questions 50 nano-molar concentration of Lucigenin, and a 50 micro-molar Clsolutions. 1000:1 ratio of Cl- to Lucigenin. This can be further reduced, but with an increased of noise to signal ratio loss Still working at concentrations that are showing very distinct patterns We are approaching the limits of detection of our instrument and operator Background Contamination of our water? Discussion Haddad and Dobble1 showed that a mixture of CrO4 and OHBSA could be used to separate a wide array of of cations and anions. • Applying the methods used, it can be shown that with few modifications, one can successfully separate mixtures of cations and anions in concentrations in the parts-per-billion (ppb) ranges. • This work focused solely on chloride (Cl-), even at the low concentrations optimum peak shape and consistent retention times were achieved. • Ok, but is it real? Still working at concentrations that are showing very distinct patterns We are approaching the limits of detection of our instrument and operator Contamination of our water? Where are we going from here? CE is going to make or break it. Buffer has been problematic Repeat of 25 nm fluorescence data set (clean it up some) Lower the Cl- : Lucigenin ratio to 1:100 (I.e. 101µM Cl-) Determine Cl specificity vs. other halide salts Acknowledgements We gratefully acknowledge the support of the Welch Foundation in the form of a Departmental Research Grant Dr. Eamonn Healy and the Saint Edward’s University chemistry faculty Mr. Jon Steuernegel, Nathan Svadlenak, Brent Polishak, et al, for their continued assistance and support