Adsorption differential pulse

Electrochemical preconcentration can be achieved in the following two different ways, depending on whether differential pulse stripping voltammetry (differential pulse ASV) or adsorption differential pulse voltammetry has been applied. 

ADPV Adsorption differential pulse voltammetry SETAAS slurry ETAAS SDCP direct slurry DCP... 

ADPCSV Adsorptive differential pulse cathodic stripping voltammetry... 

Methods for quantitative analysis of Co indude flame and graphite-furnace atomic absorption spectrometry (AAS e.g., Welz and Sperling 1999), inductively coupled plasma emission spectrometry (ICP-AES e.g., Schramel 1994), neutron activation analysis (NAA e.g., Versieck etal. 1978), ion chromatography (e.g., Haerdi 1989), and electrochemical methods such as adsorption differential pulse voltammetry (ADPV e.g., Ostapczuk etal. 1983, Wang 1994). Older photometric methods are described in the literature (e.g.. Burger 1973). For a comparative study of the most commonly employed methods in the analysis of biological materials, see Miller-Ihli and Wolf (1986) and Angerer and Schaller... 

L. Ilcheva and K. Cammann, Flow Injection Analysis of Chloride in Tap and Sewage Water Types by Adsorption Differential Pulse Voltammetry. Fresenius Z. Anal. Chem., 322 (1985) 323. 

Gammelgaard, B. and Andersen, J.R. (1985). Determination of nickel in human nails by adsorption differential-pulse voltammetry. Analyst, 110,1197. 

L. Fernandez-Llano, M.C. Blanco-Lopez, M.J. Lobo-Castanon, A.J. Miranda-Ordieres and P. Tunon-Blanco, Determination of diclofenac in urine samples by molecularly-imprinted solid-phase extraction and adsorptive differential pulse voltammetry. Electroanalysis, 19 (15) 1555-1561,2007. 

A novel sensitive and seleetive adsorptive stripping proeedure for simultaneous determination of eopper, bismuth and lead is presented. The method is based on the adsorptive aeeumulation of thymolphetalexone (TPN) eomplexes of these elements onto a hanging mereury drop eleetrode, followed by reduetion of adsorbed speeies by voltammetrie sean using differential pulse modulation. The optimum analytieal eonditions were found to be TPN eoneentration of 4.0 p.M, pH of 9.0, and aeeumulation potential at -800 mV vs. Ag/AgCl with an aeeumulation time of 80 seeonds. The peak eurrents ai e proportional to the eoneentration of eopper, bismuth and lead over the 0.4-300, 1-200 and 1-100 ng mL ranges with deteetion limits of 0.4, 0.8 and 0.7 ng mL respeetively. The proeedure was applied to the simultaneous determination of eopper, bismuth and lead in real and synthetie samples with satisfaetory results. 

In addition to chromatography based on adsorption, ion pair chromatography (IP-HPLC) and capillary electrophoresis (CE) or capillary zone electrophoresis (CZE) are new methods that became popular and are sufficiently accurate for these types of investigations. Other methods involving electrochemical responses include differential pulse polarography, adsorptive and derived voltammetry, and more recently, electrochemical sensors. 

In conclusion, synthetic dyes can be determined in solid foods and in nonalcoholic beverages and from their concentrated formulas by spectrometric methods or by several separation techniques such as TEC, HPLC, HPLC coupled with diode array or UV-Vis spectrometry, MECK, MEECK, voltammetry, and CE. ° Many analytical approaches have been used for simultaneous determinations of synthetic food additives thin layer chromatography, " " derivative spectrophotometry, adsorptive voltammetry, differential pulse polarography, and flow-through sensors for the specific determination of Sunset Yellow and its Sudan 1 subsidiary in food, " but they are generally suitable only for analyzing few-component mixtures. 

Van den Berg [510] carried out direct determinations of molybdenum in seawater by adsorption voltammetry. The method is based on complex formation of molybdenum (VI) with 8-hydroxyquinoline (oxine) on a hanging mercury drop electrode. The reduction current of adsorbed complexions was measured by differential pulse adsorption voltammetry. The effects of variation of pH and oxine concentration and of the adsorption potential were examined. The method was accurate up to 300 nmol/1. The detection limit was 0.1 nmol/1. 

Cyclohexane-1,2-dione dioxime (nioxime) complexes of cobalt (II) and nickel (II) were concentrated from 10 ml seawater samples onto a hanging mercury drop electrode by controlled adsorption. Cobalt (II) and nickel (II) reduction currents were measured by differential pulse cathodic stripping voltammetry. Detection limits for cobalt and nickel were 6 pM and 0.45 mM, respectively. The results of detailed studies for optimising the analytical parameters, namely nioxime and buffer concentrations, pH, and adsorption potential are discussed. 

Cuculic and Branica [788] used differential pulse ASV to study the adsorption of cadmium, lead, and copper on glass, quartz, and Nalgene sample containers. Nalgene was shown to be the best for sample storage, and quartz the best for electroanalytical vessels. 

Cuculic and Branica [788] applied differential pulse anodic stripping voltammetry to a study of the adsorption of cadmium, copper, and lead in seawater onto electrochemical glass vessels, quartz cells, and Nalgene sample bottles. Nalgene was best for sample storage and quartz was best for electroanalytical vessels. 

Krznaric [799] studied the influence of surfactants (EDTA, NTA) on measurements of copper and cadmium in seawater by differential pulse ASV. Adsorption of surfactants onto the electrode surface were shown to change the kinetics of the overall electrode charge and mass transfer, resulting in altered detection limits. Possible implications for studies on metal speciation in polluted seawater with high surfactant contents are outlined. 

The adsorption behavior of the psychotropic drug flunitrazepam (256) at the hanging mercury drop electrode was studied by staircase voltammetry and by adsorptive stripping differential pulse voltammetry. 256 can be determined down to nanomolar levels by using adsorptive preconcentration prior to the differential pulse voltammetry scan. The method was applied to determination of 256 in human urine530. 

Differential pulse voltammetry is particularly susceptible to adsorption of species on the electrode, which can have drastic implications for peak shape. If adsorption is suspected, then peak area should be used rather than peak height... 

Differential pulse voltammetry and electrochemical impedance have demonstrated that G, A, guanosine, and their oxidation products are electrostatically adsorbed on GC and GC(ox) surfaces [47,49]. The strength of adsorption of the DNA bases on the GC surface were found to be similar [49]. Strongly adsorbed G dimers were formed on GC between G and the adsorbed G oxidation products, which slowly cover and block the surface. The appHcation of ultrasound led to removal of the adsorbed species. The effect of this was mainly to enhance transport of electroactive species and to clean the electrode in situ, avoiding electrode fouling. 

Higuera etal. [141] have studied reduction of 4-chloro-2,6-diisopropyloamino-5-triazine in acidic media up to pH 5, applying dc differential pulse polarogra-phy. In the recorded voltammograms, two main reduction peaks were observed, with a prepeak at less negative potentials, and a postpeak at more negative potentials, what points to adsorption of the compound at the electrode. Two main peaks corresponded to two-electron reduction process. 

Recent studies describe the use of cyclic voltammetry in conjunction with controlled-potential coulometry to study the oxidative reaction mechanisms of benzofuran derivatives [115] and bamipine hydrochloride [116]. The use of fast-scan cyclic voltammetry and linear sweep voltammetry to study the reduction kinetic and thermodynamic parameters of cefazolin and cefmetazole has also been described [117]. Determinations of vitamins have been studied with voltammetric techniques, such as differential pulse voltammetry for vitamin D3 with a rotating glassy carbon electrode [118,119], and cyclic voltammetry and square-wave adsorptive stripping voltammetry for vitamin K3 (menadione) [120]. 

Stripping voltammetry has also been applied to the quantitation of the drug in formulations. A sensitive and precise method using square-wave adsorptive stripping voltammetry has been developed for the determination of sulpha-quinoxaline in veterinary formulations [157]. The differential pulse adsorptive stripping voltammetric determination of midazolam in injectable formulations as a method for quality control has been demonstrated [158]. 

AG Fogg, AA Barros, JO Cabral. Differential-pulse adsorptive stripping voltametry of food and cosmetic synthetic colouring matters and their determination and partial identification in tablet coating and cosmetics. Analyst 111 831—835, 1986. 

Electrochemical measurements have been developed by using different electrochemical techniques (differential pulse voltammetry (DPV), cyclic voltametry (CV), potentiometric stripping analysis (PSA), square wave voltammetry (SWV), adsorptive stripping transfer voltammetry (ASTV), etc.). The abbreviations given in covalent attachment of DNA onto different transducers are water soluble carbodimide l-(3-dimethyaminopropyl)-3-ethyl-carbodimide (EDC), IV-hydroxysuccimide (NHS), mercaptohexanol (MCH), aminoethanethiol (AET), mercaptosilane (MSi), and N-cyclohexyl-lV -[2-(N-methylmorpholino)-ethyl]carbodimide-4-tolune sulfonate (CDS). 

Far from the metal trace analysis, our initial studies with BCFMEs were focused on the determination of folic acid [122], In this case, the main goal was the optimisation of the electrode pretreatment for this analyte. An acidic medium (0.1M perchloric acid) was considered optimum for folic acid determination by differential pulse voltammetry. A linear range between 2.0 x HT8 and 1.0 x 10 6M with a detection limit of 1.0 x 10 8M was obtained. Nevertheless, in this work, the adsorptive properties of the folic acid on mercury were noted and the employment of mercury-coated carbon fibre UMEs for folic acid determination has been targeted as a future goal. 

Differential pulse polarography [51] and adsorption voltammetry [52] have both been employed for the determination of nickel in plant tissues. 

Fig. 14.22. Differential pulse voltammogram of GO and FAD on a gold electrode, a, Background current b, after 10 min adsorption of the enzyme from 5.3 iM solution c, after 40 min d, after 120 min e, electrochemical response of adsorbed FAD measured in pure buffer after 2 hr adsorption from 10 iM FAD solution and washing the electrode. (Reprinted from A. Szucs, G. D. Hitchens, and J. O M. Bockris, Bioelectrochemistry 21 133, copyright 1989. Reproduced with permission of Elsevier Science.)...

Some similar features were observed concerning the adsorption and electrochemical oxidation of DNA on glassy carbon and tin oxide electrodes [68]. Differential pulse voltammograms were recorded in buffer solution without DNA after adsorption of DNA onto the electrode surface during a predetermined time at a fixed potential suggesting the possibility of using adsorption to preconcentrate DNA on solid electrode surfaces and use this DNA-modified electrode for analytical purposes. 

---