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Sample records for adsorptive stripping voltammetric

  1. Adsorptive stripping voltammetric determination of trace amounts of lead in environmental water samples with complicated matrix

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    Grabarczyk M.

    2013-04-01

    Full Text Available A sensitive, simple and fast adsorptive stripping voltammetric procedure for trace determination of lead in environmental water samples has been developed. The method is based on adsorptive accumulation of the Pb(II-cupferron complex onto a hanging mercury drop electrode, followed by the reduction of the adsorbed species by a voltammetric scan using differential pulse modulation. The interference from surface active substances was eliminated by adsorption of interferents onto an Amberlite XAD-16 resin. Optimumconditions for removing the surfactants by mixing the analysed sample with resin were evaluated. The accuracy of the method was tested by analyzing certified reference material (SPS-WW1 Waste Water.

  2. Adsorptive stripping voltammetric determination of chromium in gallium.

    Science.gov (United States)

    Palrecha, M M; Mathur, P K

    1997-12-19

    The electroanalytical chemistry of trace metals has progressed strongly with the development of cathodic stripping voltammetry (CSV) preceded by adsorption collection of organic metal complexes. A sensitive method for the determination of trace amount of chromium in gallium is described. Gallium is dissolved in sodium hydroxide containing hydrogen peroxide. The method is based on the catalytic activity of nitrate ions on the reduction of Cr(III)TTHA (triethylene tetramine-N,N,N',N'',N''',N'''-hexaacetic acid) complex. The sensitivity of this method is further improved by adsorption preconcentration of Cr(III)TTHA complex at a hanging mercury drop electrode (HMDE). The Cr(III) formed at the electrode surface by the reduction of Cr(VI), which is present in the bulk solution, is immediately complexed by TTHA. The adsorbed complex is then reduced at a peak potential of - 1.26 V, and the peak height of Cr(III) reduction is measured. The determination limit was restricted by the amount of chromium present in the reagent blank solution. The method is suitable for the determination of chromium at level as low as 0.2 mug g(-1) (with about 50 mg of sample) and a relative standard deviation of 15%.

  3. Adsorptive Cathodic Stripping Voltammetric Determination of Cefoperazone in Bulk Powder, Pharmaceutical Dosage Forms, and Human Urine

    Science.gov (United States)

    Hoang, Vu Dang; Huyen, Dao Thi; Phuc, Phan Hong

    2013-01-01

    The electroreduction behaviour and determination of cefoperazone using a hanging mercury drop electrode were investigated. Cyclic voltammograms of cefoperazone recorded in universal Britton-Robinson buffers pH 3–6 exhibited a single irreversible cathodic peak. The process was adsorption-controlled. Britton-Robinson buffer 0.04 M pH 4.0 was selected as a supporting electrolyte for quantitative purposes by differential pulse and square wave adsorptive cathodic stripping voltammetry. The experimental voltammetric conditions were optimized using Central Composite Face design. A reduction wave was seen in the range from −0.7 to −0.8 V. These voltammetric techniques were successfully validated as per ICH guidelines and applied for the determination of cefoperazone in its single and sulbactam containing powders for injection and statistically comparable to USP-HPLC. They were further extended to determine cefoperazone in spiked human urine with no matrix effect. PMID:24109542

  4. Adsorptive Cathodic Stripping Voltammetric Determination of Cefoperazone in Bulk Powder, Pharmaceutical Dosage Forms, and Human Urine

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    Vu Dang Hoang

    2013-01-01

    Full Text Available The electroreduction behaviour and determination of cefoperazone using a hanging mercury drop electrode were investigated. Cyclic voltammograms of cefoperazone recorded in universal Britton-Robinson buffers pH 3–6 exhibited a single irreversible cathodic peak. The process was adsorption-controlled. Britton-Robinson buffer 0.04 M pH 4.0 was selected as a supporting electrolyte for quantitative purposes by differential pulse and square wave adsorptive cathodic stripping voltammetry. The experimental voltammetric conditions were optimized using Central Composite Face design. A reduction wave was seen in the range from −0.7 to −0.8 V. These voltammetric techniques were successfully validated as per ICH guidelines and applied for the determination of cefoperazone in its single and sulbactam containing powders for injection and statistically comparable to USP-HPLC. They were further extended to determine cefoperazone in spiked human urine with no matrix effect.

  5. Adsorptive cathodic stripping voltammetric determination of cefoperazone in bulk powder, pharmaceutical dosage forms, and human urine.

    Science.gov (United States)

    Hoang, Vu Dang; Huyen, Dao Thi; Phuc, Phan Hong

    2013-01-01

    The electroreduction behaviour and determination of cefoperazone using a hanging mercury drop electrode were investigated. Cyclic voltammograms of cefoperazone recorded in universal Britton-Robinson buffers pH 3-6 exhibited a single irreversible cathodic peak. The process was adsorption-controlled. Britton-Robinson buffer 0.04 M pH 4.0 was selected as a supporting electrolyte for quantitative purposes by differential pulse and square wave adsorptive cathodic stripping voltammetry. The experimental voltammetric conditions were optimized using Central Composite Face design. A reduction wave was seen in the range from -0.7 to -0.8 V. These voltammetric techniques were successfully validated as per ICH guidelines and applied for the determination of cefoperazone in its single and sulbactam containing powders for injection and statistically comparable to USP-HPLC. They were further extended to determine cefoperazone in spiked human urine with no matrix effect.

  6. Cathodic adsorptive stripping voltammetric determination of Ribavirin in pharmaceutical dosage form, urine and serum

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    Ahmed A. Abdel Gaber

    2017-05-01

    Full Text Available A sensitive, simple and rapid square-wave adsorptive stripping voltammetric method was developed and validated for the determination of Ribavirin in pharmaceutical formulations. The proposed method was based on the electrochemical reduction of Ribavirin at a hanging mercury drop electrode in Britton Robinson buffer at pH 10. A well-defined peak was observed at 880 mV with 30 s of accumulation time and 50 mV of accumulation potential. Under these optimized conditions, the square-wave adsorptive stripping voltammetric peak current showed a linear correlation on drug concentration over the range of 1 × 10−10–2 × 10−7 mol L−1 with a correlation coefficient of 0.9995 for the proposed method. The detection and quantitation limits for this method were 2.02 × 10−10 and 6.80 × 10−10 mol L−1, respectively. The results obtained for intra-day and inter-day precision (as RSD % were between 0.447% and 1.024%. This method was applied successfully for the determination of Ribavirin in its pharmaceutical dosage forms with mean recoveries of 99.68 ± 0.13 with RSD % of 0.81% and 99.20 ± 0.24 with RSD % of 0.49% for two concentrations 5 × 10−9 and 5 × 10−8 mol L−1, respectively for 200 mg capsules. The results obtained from the developed square-wave adsorptive stripping voltammetric method were compared with those obtained by the analytical method reported in the literature.

  7. Adsorptive stripping voltammetric determination of the antidepressant drug sulpiride.

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    Farghaly, O A

    2000-10-01

    The electrochemical behaviour of the antidepressant drug sulpiride (SP) at a hanging mercury drop electrode (HMDE) is investigated. Linear sweep cathodic stripping voltammetry (LSCSV) was used to determine sulpiride in the presence of 0.01 M sodium acetate medium pH 10.5 and 25 +/- 1 degrees C. Different parameters such as, supporting electrolyte, pH, accumulation potential, scan rate, accumulation time and ionic strength, were tested to optimize the conditions for the determination of SP. The adsorbed form is reduced irreversibly. The linear concentration range is from 2 x 10(-9) to 5 x 10(-8) M SP. Experimentally, 2 x 10(-9) M (0.68 ppb) with accumulation time 60 s can be determined successfully. Furthermore, a theoretical detection limit of 2 x 10(-10) M (0.068 ppb) Sp was calculated. The interferences of some metal ions, ascorbic acid and some amino acids were studied. The method was applied to the analysis of tablets and spiked urine, with recoveries of 104 +/- 3 and 101 + 3, and the relative standard deviation of 3.3 and 3.4%, respectively.

  8. Adsorptive cathodic stripping voltammetric determination of dexamethasone in formulations and biological fluids.

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    Ghoneim, Enass M; El-Attar, Mona A; Ghoneim, Mohamed M

    2009-01-01

    The electrochemical behavior of dexamethasone at a hanging mercury drop electrode (HMDE) in a universal buffer series of pH 2-10 was studied using cyclic voltammetry. Based on the interfacial adsorptive character of dexamethasone onto the HMDE (electrode surface coverage = 1.4 x 10(-10) mol/cm2), a fully validated simple square-wave adsorptive cathodic stripping voltammetric method is described for its determination in bulk form with a limit of detection (LOD) of 3.1 x 10(-9) M. The described method was successfully applied to analysis of dexamethasone in its pharmaceutical formulations (deltasone tablets and fortecortin ampule) and in spiked samples of human urine, bovine urine, and protein-free bovine milk. The achieved LODs of dexamethasone in human urine, bovine urine, and protein-free bovine milk were 1.5 x 10(-8), 2 x 10(-8), and 9 x 10(-9) M, respectively. The mean percentage recoveries of 4 x 10(-7) M dexamethasone in bulk form, spiked human urine, bovine urine, and bovine milk, based on the average of 3 replicate measurements, were 99.8 +/- 0.25, 100.4 +/- 0.96, 99.6 +/- 0.79, and 100.1 +/- 0.26, respectively.

  9. Adsorptive stripping voltammetric determination of netilmicin in the presence of formaldehyde.

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    Sun, Nan; Mo, Weimin; Hu, Baoxiang; Shen, Zhenlu

    2006-05-01

    A linear sweep adsorptive stripping voltammetric method for the determination of netilmicin in the presence of formaldehyde has been proposed for the first time. In the presence of 3.0 x 10(-3) g ml(-1) formaldehyde, netilmicin exhibits a sensitive cathodic peak at -1.30 V (vs. the saturated calomel electrode, SCE) in a medium of Britton-Robinson buffer (pH 8.7) with a scan rate of 100 mV s(-1) after a preconcentration period of 120 s at -1.10 V (vs. SCE). The peak current showed a linear dependence on the netilmicin concentration over the range 4.2 x 10(-9)-1.0 x 10(-7) g ml(-1). The achieved limits of detection and quantitation were 1.0 x 10(-10) and 3.3 x 10(-10) g ml(-1) netilmicin, respectively. It was deduced from the experiments that the amine-aldehyde condensation product formed between netilmicin and formaldehyde is mainly responsible for the appearance of the peak. The electrochemical behavior of netilmicin in the presence of formaldehyde has been studied. The method was applied to the direct determination of netilmicin in injectable formulations and spiked human urine and serum samples.

  10. Adsorptive Stripping Voltammetric Determination of Hydroquinone using an Electrochemically Pretreated Glassy Carbon Electrode

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    Abdul Niaz1,

    2008-12-01

    Full Text Available A simple and efficient adsorptive stripping voltammetric (AdSV method was developed for the determination of hydroquinone at an electrochemically pretreated glassy carbon (GC electrode in waste water. Various parameters such as solvent system, accumulation potential, accumulation time and scan rate were optimized. The electrochemically pretreated GC electrode showed good response towards hydroquinone determination by using AdSV. Under the optimized conditions the peak current showed good linear relationship with the hydroquinone concentration in the range of 0.5-4.0mg L-1 and 5-30mg L-1. The 60/40 methanol/water composition was found to be the best solvent system and 0.05mol L-1 H2SO4 was found as useful supporting electrolyte concentration. The accumulation time was 60 s and the detection limit was 50µg L-1. The developed method was successfully applied for the determination of hydroquinone in polymeric industrial discharge samples waste photographic developer solution and cream sample without any significant effect of surface fouling.

  11. Preparation of NiO-graphene oxide nanosensor for adsorptive stripping voltammetric determination of dinoterbon in food samples

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    Kasaram Roja

    2016-09-01

    Full Text Available Graphene oxide (GO modified NiO electrochemical nanosensor was developed for the determination of the dinoterbon in food samples using adsorptive stripping voltammetry. The modified nanosensor characterized by TEM, XRD, cyclic and adsorptive stripping voltammetry. Dinoterbon pesticide exhibited a single well-defined cathodic peak at pH 4.0 at Britton–Robinson buffer (-810.0 mV. The voltammetric characterization of the pesti­cide residues is evaluated and the parameter such as the effect of pH, scan rate, pulse amplitude, deposition potential and deposition time were optimized. The current–concen­tration plot obtained using this peak was straight-lined over the range from 0.05 to 50.00 µg mL-1 with limit of detection (LOD 0.028 µg mL-1. The proposed method was efficiently applied to the determination of dinoterbon in food samples. The mean recoveries of the pesticide 97.40 to 99.88 % with a relative standard deviation of 0.114 % in food samples respectively.

  12. Simultaneous voltammetric determination of morphine and noscapine by adsorptive differential pulse stripping method and least-squares support vector machines.

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    Niazi, Ali; Ghasemi, Jahanbakhsh; Zendehdel, Mojgan

    2007-11-30

    An adsorptive differential pulse stripping method for the simultaneous determination of morphine and noscapine is proposed. The procedure involves an adsorptive accumulation of morphine and noscapine on a hanging mercury drop electrode (HMDE), followed by oxidation of adsorbed morphine and noscapine by voltammetric scan using differential pulse modulation. The optimum experimental conditions are: pH 10.0, accumulation potential of -100 mV versus Ag/AgCl, accumulation time of 150 s, scan rate of 40 mV s(-1) and pulse height of 100 mV. Morphine and noscapine peak currents were observed in same potential region at about +0.25 V. The simultaneous determination of morphine and noscapine by using voltammetry is a difficult problem in analytical chemistry, due to voltammogram interferences. The resolution of mixture of morphine and noscapine by the application of least-squares support vector machines (LS-SVM) was performed. The linear dynamic ranges were 0.01-3.10 and 0.015-2.75 microg mL(-1) and detection limits were 3 and 7 ng mL(-1) for morphine and noscapine, respectively. The capability of the method for the analysis of real samples was evaluated by the determination of morphine and noscapine in addict's human plasma with satisfactory results.

  13. A Validated Adsorptive Stripping Voltammetric Determination of Antidiabetic Agent Pioglitazone HCl in Tablets and Biological Fluids

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    Al-Arfaj, Nawal Ahmad; Al-Abdulkareem, Eman Abdullah; Aly, Fatma Ahmad

    2008-01-01

    Square-wave adsorptive cathodic stripping voltammetry was used to determine pioglitazone HCl in Britton Robinson buffer of pH5. The adsorptive cathodic peak was observed at -1.5 V vs. Ag/AgCl. The peak response was characterized with respect to pH, supporting electrolyte, frequency, scan increment, pulse-amplitude, accumulation potential and pre-concentration time. Under optimal conditions, the peak current is proportional to the concentration of pioglitazone HCl, and a linear calibration graphs were obtained within the concentration levels of 10-8 and 10-4 M following different accumulation time periods (0-300 s). The obtained results were analyzed and the statistical parameters were calculated. The detection limit is 8.08 × 10-9 M (3.17 ng ml-1) using 300 s pre-concentration time, whereas the quantitative limit is 2.45 × 10-8 M (9.63 ng ml-1). The proposed method was applied to assay the drug in pharmaceutical formulations and biological fluids. The pharmacokinetic parameters of drug in human plasma were estimated as: Cmax=785.8 ng ml-1, tmax=1.5 h, Ke=0.125 h-1 and t1/2=8 h which are favorably compared with those reported in literature. PMID:23675103

  14. Adsorptive stripping voltammetric determination of nitroimidazole derivative on multiwalled carbon nanotube modified electrodes: influence of size and functionalization of nanotubes

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    Jara-Ulloa, Paola; Canete-Rosales, Paulina; Nunez-Vergara, Luis J; Squella, Juan A., E-mail: asquella@ciq.uchile.c [University of Chile, Santiago (Chile). Chemical and Pharmaceutical Sciences Faculty. Bioelectrochemistry Lab.

    2011-07-01

    1-Methyl-4-nitro-2-bromine methylimidazole (4-NimMeBr), was electrochemically reduced on mercury, glassy carbon and multiwalled carbon nanotubes (MWCNT) modified electrodes. 4-NimMeBr was adsorbed on the MWCNT modified electrode thus permitting the implementation of an adsorptive stripping voltammetric (ASV) method. We have used 4-NimMeBr as a prototype electroactive nitro compound to study the effect of both the size of the nanotubes and its functionalization by oxidation. The oxidized MWCNT forms better dispersions than the non-oxidized, producing electrode surface with higher density of MWCNT as was determined by electrochemical mapping using scanning electrochemical microscopy (SECM). Under the optimized conditions, the peak current was proportional to the concentration of 4-NimMeBr in the range of 10{sup -6} mol L{sup -1} to 10{sup -4} mol L{sup -1} with detection and quantification limits of 4.41 x 10{sup -6} mol L{sup -1} and 6.21 x 10{sup -6} mol L{sup -1}, respectively. The sensibility of bare electrode was 0.01 {mu}A per mmol L{sup -1}, which was lower than the value of 5.34 and 6.97 mA per mmol L{sup -1} obtained using short and large oxidized MWCNT, respectively. (author)

  15. Adsorptive Cathodic Stripping Voltammetric Method with Alizarin for the Simultaneous Determination of Cadmium, and Zinc in Water Samples

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    Deswati

    2016-12-01

    Full Text Available This paper reports on the development of adsorptive cathodic stripping voltammetric (AdCSV method with 1,2-dihydroxyanthraquinone or Alizarin (AZ as a complexing agent used in the simultaneous determination of ultra trace of Cd and Zn because it has a good sensitivity, and selectivity. The influence of several parameters was studied: the effects of 1,2-dihydroxyanthraquinone or Alizarin (AZ concentration, pH, accumulation potential, and accumulation time. The relative standard deviation (RSD, and recovery is determined to get the accuracy and precision method. It also determined the limit of detection (LOD of the method to get the sensitivity. In this case, the optimum conditions were AZ concentration of 0.5 mM, pH 5, step deposition (70 s, -0.5 V. This method has been applied in water samples successfully, was obtained (Cd 23, and Zn 124 µg/L, LOD (Cd 0.006, and Zn 0.004 µg/L, RSD (Cd 0.4, and Zn 1.4 % (n = 10, recovery (Cd 99.36, and Zn 99.28%. The Atomic absorption spectrometric (AAS method is used as a comparison AdCSV optimum, was obtained (Cd 16, and Zn 115 µg/L.

  16. A square-wave adsorptive stripping voltammetric method for the determination of Amaranth, a food additive dye.

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    Alghamdi, Ahmad H

    2005-01-01

    Square-wave adsorptive stripping voltammetric (AdSV) determinations of trace concentrations of the azo coloring agent Amaranth are described. The analytical methodology used was based on the adsorptive preconcentration of the dye on the hanging mercury drop electrode, followed by initiation of a negative sweep. In a pH 10 carbonate supporting electrolyte, Amaranth gave a well-defined and sensitive AdSV peak at -518 mV. The electroanalytical determination of this azo dye was found to be optimal in carbonate buffer (pH 10) under the following experimental conditions: accumulation time, 120 s; accumulation potential, 0.0 V; scan rate, 600 mV/s; pulse amplitude, 90 mV; and frequency, 50 Hz. Under these optimized conditions the AdSV peak current was proportional over the concentration range 1 x 10(-8)-1.1 x 10(-7) mol/L (r = 0.999) with a detection limit of 1.7 x 10(-9) mol/L (1.03 ppb). This analytical approach possessed enhanced sensitivity, compared with conventional liquid chromatography or spectrophotometry and it was simple and fast. The precision of the method, expressed as the relative standard deviation, was 0.23%, whereas the accuracy, expressed as the mean recovery, was 104%. Possible interferences by several substances usually present as food additive azo dyes (E110, E102), gelatin, natural and artificial sweeteners, preservatives, and antioxidants were also investigated. The developed electroanalyticals method was applied to the determination of Amaranth in soft drink samples, and the results were compared with those obtained by a reference spectrophotometric method. Statistical analysis (paired t-test) of these data showed that the results of the 2 methods compared favorably.

  17. Adsorptive stripping differential pulse voltammetric determination of venlafaxine and desvenlafaxine employing Nafion-carbon nanotube composite glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Sanghavi, Bankim J. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400 098, Maharashtra (India); Srivastava, Ashwini K., E-mail: aksrivastava@chem.mu.ac.i [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400 098, Maharashtra (India)

    2011-04-15

    A Nafion-carbon nanotube-modified glassy carbon electrode (NAF-CNT-GCE) was developed for the determination of venlafaxine (VF) and desvenlafaxine (DVF). The electrochemical behavior of both these molecules was investigated employing cyclic voltammetry (CV), chronocoulometry (CC), electrochemical impedance spectroscopy (EIS) and adsorptive stripping differential pulse voltammetry (AdSDPV). The surface morphology of the electrodes has been studied by means of scanning electron microscopy (SEM). These studies revealed that the oxidation of VF and DVF is facilitated at NAF-CNT-GCE. After optimization of analytical conditions employing this electrode at pH 7.0 in Britton-Robinson buffer (0.05 M) for VF and pH 5.0 in acetate buffer (0.1 M) for DVF, the peak currents for both the molecules were found to vary linearly with their concentrations in the range of 3.81 x 10{sup -8}-6.22 x 10{sup -5} M for VF and 5.33 x 10{sup -8}-3.58 x 10{sup -5} M for DVF. The detection limits (S/N = 3) of 1.24 x 10{sup -8} and 2.11 x 10{sup -8} M were obtained for VF and DVF, respectively, using AdSDPV. The prepared modified electrode showed several advantages, such as simple preparation method, high sensitivity, very low detection limits and excellent reproducibility. The proposed method was employed for the determination of VF and DVF in pharmaceutical formulations, urine and blood serum samples.

  18. The renewable bismuth bulk annular band working electrode: fabrication and application in the adsorptive stripping voltammetric determination of nickel(II) and cobalt(II).

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    Baś, Bogusław; Węgiel, Krystian; Jedlińska, Katarzyna

    2015-06-30

    The paper presents the first report on fabrication and application of a user friendly and mercury free electrochemical sensor, with the renewable bismuth bulk annular band working electrode (RBiABE), in stripping voltammetry (SV). The sensor body is partly filled with the internal electrolyte solution, in which the RBiABE is cleaned and activated before each measurement. Time of the RBiABE contact with the sample solution is precisely controlled. The usefulness of this sensor was tested by Ni(II) and Co(II) traces determination by means of differential pulse adsorptive stripping voltammetry (DP AdSV), after complexation with dimethylglyoxime (DMG) in ammonia buffer (pH 8.2). The experimental variables (composition of the supporting electrolyte, pre-concentration potential and time, potential of the RBiABE activation, and DP parameters), as well as possible interferences, were investigated. The linear calibration graphs for Ni(II) and Co(II), determined individually and together, in the range from 1×10(-8) to 70×10(-8)molL(-1) and from 1×10(-9) to 70×10(-9)molL(-1) respectively, were obtained. The calculated limit of detection (LOD), for 30s of the accumulation time, was 3×10(-9)molL(-1) for Ni(II) in case of a single element's analysis, whereas the LOD was 5×10(-9)molL(-1) for Ni(II) and 3×10(-10)molL(-1) for Co(II), when both metal ions were measured together. The repeatability of the Ni(II) and Co(II) adsorptive stripping voltammetric signals obtained at the RBiABE were equal to 5.4% and 2.5%, respectively (n=5). Finally, the proposed method was validated by determining Ni(II) and Co(II) in the certified reference waters (SPS-SW1 and SPS-SW2) with satisfactory results.

  19. Voltammetric characteristics of miconazole and its cathodic stripping voltammetric determination

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    FRANCISCO C. PEREIRA

    2002-09-01

    Full Text Available Miconazole is reduced at mercury electrode above pH 6 involving organometallic compound formation, responsible for an anomalous polarographic behavior. The electrodic process presents a large contribution of the adsorption effects. The drug can be determined by cathodic stripping voltammetry from 8.0 x 10-8 to 1, 5 x 10-6 molL-1 in Britton-Robinson buffer pH 8.0, when pre-accumulated for 30s at an accumulation potential of 0V. A relative standard deviation of 3.8% was obtained for ten measurements of 1.0 x 10-7 molL-1 miconazole in B-R buffer pH 8.0 and a limit detection of 1, 7 x 10-8 molL-1 was determined using 60s of deposition time and scan rate of 100 mVs-1. The proposed method is simple, precise and it was applied successfully for the determination of the miconazole in pure form and in commercial formulations, showing mean recoveries of 99.7-98.4%.Miconazol é reduzido no eletrodo de mercúrio em valor de pH acima de 6,0 envolvendo formação de composto organometálico, responsável por um comportamento polarográfico anômalo. O processo eletródico apresenta uma larga contribuição de efeitos de adsorção. A droga pode ser determinada por voltametria de redissolução catódica de 8, 0 x 10-8 a 1, 5 x 10-6 mol L-1 em tampão Britton-Robinson pH 8,0 quando pré-acumulada por 30s em potencial de acúmulo de 0V. Um desvio padrão relativo de 3,8% foi obtido de 10 medidas de 1, 0 x 10-7 mol L-1 de miconazol em tampão B-R pH 8,0 e um limite de detecção de 1, 7 x 10-8 mol L-1 foi determinado usando 60s de tempo de deposição e velocidade de varredura de 100 mV s-1. O método proposto é simples, preciso e foi aplicado com sucesso para a determinação de miconazol na forma pura e em formulações comerciais, mostrando médias de recuperação de 99, 7 - 98, 4%.

  20. Stripping voltammetric detection of nephrotoxic drug cefitizoxime in wastewater

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    Jahangir Ahmad Rather

    2015-06-01

    Full Text Available The objective of the present work is to develop the stripping voltammetric method for determination of nephrotoxic drug cefitizoxime in pharmaceutical formulation and its application to wastewater analysis. Solubilized system of different surfactants viz. cationic, anionic and non-ionic influences the electrochemical response of cefitizoxime. Solubilized system of CTAB containing cefitizoxime enhanced the peak current while anionic and non-ionic showed an opposite effect. The current signal due to the reduction process is a function of concentration of the cefitizoxime, pH of medium, type of surfactant and accumulation time at electrode surface. The proposed SWCAdSV (Squarewave Cathodic Adsorptive Voltammtery and DPCAdSV (Differential Pulse Cathodic Adsorptive Voltammetry are linear over concentration range 1.732–6.901 μg/mL and 4.792–30.672 μg/mL with detection limit of 0.76 ng/mL and 2.63 ng/mL, respectively. The method is successfully applied for determination of cefitizoxime in pharmaceutical formulation and wastewater with mean percentage recovery of 99.73% and 98.51%, respectively.

  1. Adsorptive stripping voltammetric determination of imipramine, trimipramine and desipramine employing titanium dioxide nanoparticles and an Amberlite XAD-2 modified glassy carbon paste electrode.

    Science.gov (United States)

    Sanghavi, Bankim J; Srivastava, Ashwini K

    2013-03-07

    An Amberlite XAD-2 (XAD2) and titanium dioxide nanoparticles (TNPs) modified glassy carbon paste electrode (XAD2-TNP-GCPE) was developed for the determination of imipramine (IMI), trimipramine (TRI) and desipramine (DES). The electrochemical behavior of these molecules was investigated employing cyclic voltammetry (CV), chronocoulometry (CC), electrochemical impedance spectroscopy (EIS) and adsorptive stripping differential pulse voltammetry (AdSDPV). After optimization of analytical conditions using a XAD2-TNP-GCPE electrode at pH 6.0 phosphate buffer (0.1 M), the peak currents were found to vary linearly with its concentration in the range of 1.30 × 10(-9) to 6.23 × 10(-6) M for IMI, 1.16 × 10(-9) to 6.87 × 10(-6) M for TRI and 1.43 × 10(-9) to 5.68 × 10(-6) M for DES. The detection limits (S/N = 3) of 3.93 × 10(-10), 3.51 × 10(-10) and 4.35 × 10(-10) M were obtained for IMI, TRI and DES respectively using AdSDPV. The prepared modified electrode showed several advantages such as a simple preparation method, high sensitivity, very low detection limits and excellent reproducibility. The proposed method was employed for the determination of IMI, TRI and DES in pharmaceutical formulations, blood serum and urine samples.

  2. Optimization and validation of an automated voltammetric stripping technique for ultratrace metal analysis

    Energy Technology Data Exchange (ETDEWEB)

    Monticelli, D. [Dipartimento di Scienze Chimiche e Ambientali, Universita degli Studi dell' Insubria, Via Valleggio 11, 22100 Como (Italy)]. E-mail: damiano.monticelli@uninsubria.it; Ciceri, E. [Dipartimento di Scienze Chimiche e Ambientali, Universita degli Studi dell' Insubria, Via Valleggio 11, 22100 Como (Italy); Dossi, C. [Dipartimento di Scienze Chimiche e Ambientali, Universita degli Studi dell' Insubria, Via Valleggio 11, 22100 Como (Italy)

    2007-07-02

    A new automated batch method for the determination of ultratrace metals (nanogram per liter level) was developed and validated. Instrumental and chemical parameters affecting the performance of the method were carefully assessed and optimized. A wide range of voltammetric methods under different chemical conditions were tested. Cadmium, lead and copper were determined by anodic stripping voltammetry (ASV), while nickel, cobalt, rhodium and uranium by adsorptive cathodic stripping voltammetry (AdCSV). The figures of merit of all of these methods were determined: very good precision and accuracy were achieved, e.g. relative percentage standard deviation in the 4-13% for ASV and 2-5% for AdCSV. The stripping methods were applied to the determination of cadmium, lead, copper, nickel, cobalt, rhodium and uranium in lake water samples and the results were found to be comparable with ICP-MS data.

  3. Electrochemical reduction and cathodic stripping voltammetric determination of clotrimazole

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    Pereira Francisco C.

    2001-01-01

    Full Text Available The reduction of clotrimazole at a mercury electrode, in phosphate buffer, pH>6, involves a reversible one-electron process. The electrochemical process presents a large contribution from adsorption effects. For the differential pulse polarographic determination the addition of Triton X-100 is recommended. Clotrimazole can be determined by cathodic stripping voltammetry at 50 ng mL-1 level when pre-accumulated for 3 min at an accumulation potential of -0.20 V. The proposed method is applied successfully for the determination of clotrimazole in a commercial formulation.

  4. Modification of carbon screen-printed electrodes by adsorption of chemically synthesized Bi nanoparticles for the voltammetric stripping detection of Zn(II), Cd(II) and Pb(II).

    Science.gov (United States)

    Rico, Ma Angeles Granado; Olivares-Marín, Mara; Gil, Eduardo Pinilla

    2009-12-15

    A simple procedure for the chemical synthesis of bismuth nanoparticles and subsequent adsorption on commercial screen-printed carbon electrodes offer reliable quantitation of trace zinc, cadmium and lead by anodic stripping square-wave voltammetry in nondeareated water samples. The influence of two hydrodynamic configurations (convective cell and flow cell) and the effect of various experimental variables upon the stripping signals at the bismuth-coated sensor are explored. The square-wave peak current signal is linear over the low ng mL(-1) range (120 s deposition), with detections limits ranging from 0.9 to 4.9 ng mL(-1) and good precision. Applicability to waste water certified reference material and drinking water samples is demonstrated. The attractive behaviour of the new disposable Bi nanoparticles modified carbon strip electrodes, coupled with the negligible toxicity of bismuth, hold great promise for decentralized heavy metal testing in environmental and industrial effluents waters.

  5. Adsorption of pyrantel pamoate on mercury from aqueous solutions: studies by stripping voltammetry.

    Science.gov (United States)

    Gupta, Vinod K; Jain, Rajeev; Jadon, N; Radhapyari, K

    2010-10-01

    Adsorption and electrochemical reduction of pyrantel pamoate are studied in Britton Robinson buffer medium at hanging mercury drop electrode (HMDE) by Adsorptive Stripping Voltammetric technique. The peak current shows a linear dependence with the drug concentration over the range 250 ng mL(-1) to 64 microg mL(-1). Applicability to assay the drug in urine samples is illustrated in the concentration range 5-20 microg mL(-1).

  6. Determination of cobalt and nickel in biological materials using catalytic adsorptive stripping voltammetry

    OpenAIRE

    Bobrowski, Andrzej; Zarębski, Jerzy; Królicka, Agnieszka

    2012-01-01

    The paper discusses the utilisation of the catalytic adsorptive stripping voltammetric method for the simultaneous determination of Co and Ni in biological materials such as hair, oyster tissue, bovine liver and oriental tobacco leaves. For this purpose the most sensitive and selective catalytic-adsorptive system with nioxime and nitrite has been selected. The optimal parameters, including concentration of the supporting electrolyte, pH and accumulation time and potential, have be...

  7. Trends in speciation analysis of some heavy metals in serum of patients with chronic hepatitis C and chronic hepatitis B using differential pulse adsorptive stripping voltammetric measurement and atomic absorption spectrophotometry.

    Science.gov (United States)

    Rashed, Mohamed Nageeb; Ahmed, Mahasen Mohamed; Al-Hossainy, Ahmed Farouk; Abd, Safaa Mahmoud

    2010-04-01

    The relationships between chronic liver diseases and trace heavy metal contents in blood are debatable and have not been understood clearly. The present study is undertaken to determine Co, Fe, and Ni concentrations in sera from viral hepatitis patients. In all eighty patients with chronic hepatitis (B, C) and 29 healthy individuals were chosen for this study. Donors were selected from different environmental areas, including Aswan, Kom Ombo, and Edfu as polluted areas, and Daraw as an unpolluted area. Co, Fe, and Ni concentrations in patient and healthy blood serum were measured by two different analytical techniques: differential pulse adsorptive stripping voltammetry (DPA(d)SV) and atomic absorption spectrophotometer (AAS). The results reveal that Fe is present in higher level in the blood serum of hepatitis patients than in the healthy control, whereas Co and Ni showed the opposite trend. Hepatitis patients from Edfu area exhibited higher Fe level in their serum than those from the other areas, while hepatitis patients and healthy control from Daraw area (free from pollution) exhibited the lowest metal values. Patients with hepatitis C show lower levels of Co, Ni, and Fe in their serum than those with hepatitis B. A comparative study was carried out between the results using DPA(d)SV and AAS techniques, which are in very good agreements. 2009 Elsevier GmbH. All rights reserved.

  8. Cathodic adsorptive stripping square-wave voltammetry of the anti-inflammatory drug meloxicam.

    Science.gov (United States)

    Radi, A E; Ghoneim, M; Beltagi, A

    2001-10-01

    The adsorptive behavior of the anti-inflammatory drug meloxicam was studied by cyclic, differentia-pulse and square-wave voltammetry on a hanging mercury drop electrode (HMDE). The drug was accumulated at HMDE and a well-defined stripping peak current was obtained at -1.42 V vs. Ag/AgCl (saturated KCl) electrode in acetate buffer solution (pH 5.0). A voltammetric procedure was developed for the determination of meloxicam using square-wave cathodic adsorptive stripping voltammetry (SW-CASV). The optimum working conditions for the determination of the drug were established. The analysis of meloxicam in human plasma was carried out satisfactorily.

  9. SQUARE WAVE CATHODIC STRIPPING VOLTAMMETRY ADSORPTIVE FOR NICKEL AND COBALT ANALYSIS

    Directory of Open Access Journals (Sweden)

    Saryati Saryati

    2010-06-01

    Full Text Available The adsorptive stripping voltammetric determination of Ni and Co based on adsorption of the Ni/Co and dimethylglioxime (DMG complex on a hanging mercury drop electrode is studied. The reduction current of the adsorbed DMG complex is measured by square wave cathodic stripping voltammetry method. The effect of various parameters such as ligand concentration, pH of supporting electrolytic, adsorption potential and adsorption time on the current peak of Ni and Co voltammogram were studied. Optimum condition of this method are supporting electrolyte pH 9, DMG concentration 5×10 -4 M, adsorption potential -0.7 V vs Ag/AgCl and adsorption time 180 second. A linier relationship between the current peak and Ni or Co concentration was obtained in the range 5 - 30 ng/mL and the detection limit 0.6 ng/ml for both Ni and Co. The recovery of Ni and Co were 98.11-104.17% using standard biological materials with RSD 2.59 - 10.37%. Based on ";t"; test can be conclude that the result are nearly equal to the standard reference material.   Keywords: adsorptive stripping voltammetric, dimethylglioxime complex, nickel, cobalt

  10. Adsorptive stripping voltammetry of trimethoprim: mechanistic studies and application to the fast determination in pharmaceutical suspensions.

    Science.gov (United States)

    Carapuça, Helena M; Cabral, David J; Rocha, Luciana S

    2005-06-15

    The adsorptive stripping voltammetric behaviour of trimethoprim (TMP) was studied at pH 3.8 and 7.0 by linear-sweep (LS) and cyclic voltammetry at the hanging mercury drop electrode. The charges and surface concentrations of the protonated TMP species were determined at both pH values. Taking advantage of the adsorption features of TMP fast voltammetric techniques (LS and square-wave (SW) voltammetry) were applied to the determination of TMP at the 10(-7)mol dm(-3) concentration level (pH 3.8). For these concentrations the relative standard deviations were cathodic stripping voltammetry originated a very fast and sensitive method for the direct analysis of TMP in pharmaceutical suspensions without any matrix effects or interference from sulfamethoxazole. No sample pre-treatments or solvent extraction procedures were needed. The quantitative results were in agreement with the data supplied by the manufacturer.

  11. Anodic stripping voltammetric determination of Zn, Pb and Cu traces in whisky samples

    Energy Technology Data Exchange (ETDEWEB)

    Barbeira, P.J.S. [Departamento de Quimica - ICEx - UFMG, Belo Horizonte, MG (Brazil); Stradiotto, N.R. [Departamento de Quimica - FFCLRP - USP, Ribeirao Preto, SP (Brazil)

    1998-07-01

    The simultaneous ``in natura`` determination of trace Zn, Pb and Cu in whisky samples by anodic stripping voltammetry (ASV), using a hanging mercury drop electrode, without previous treatment or addition of supporting electrolyte is described. The choice of an appropriate stripping voltammetric method and deposition potential minimizes the influence of the organic content and ensures a good reproducibility of the measurements. The reliability of the method was tested comparing the results with those of atomic absorption spectroscopy (AAS), with differences of about 10%. The method allows the determination of heavy metal ions in the {mu}g L{sup -1} range. (orig.) With 3 figs., 1 tab., 18 refs.

  12. Application of experimental design on determination of aluminum content in saline samples by adsorptive cathodic stripping voltammetry

    OpenAIRE

    YILMAZ, Sinan; Öztürk, Betül; ÖZDEMİR, Durmuş

    2013-01-01

    Adsorptive cathodic stripping voltammetric determination of aluminum at ng mL-1 levels in salt samples based on the metal complexation with Calcon (1-(2-hydroxynaphthylazo)-2 naphthol-4-sulfonic acid) and the subsequent adsorptive deposition onto a hanging mercury drop electrode was studied. Central composite design was used as a design method. Several chemical and instrumental parameters (pH, ligand concentration, deposition time, deposition potential, and complexing time) were invo...

  13. Stripping voltammetric determination of mercury(II) at antimony-coated carbon paste electrode.

    Science.gov (United States)

    Ashrafi, Amir M; Vytřas, Karel

    2011-10-15

    A new procedure was elaborated to determine mercury(II) using an anodic stripping square-wave voltammetry at the antimony film carbon paste electrode (SbF-CPE). In highly acidic medium of 1M hydrochloric acid, voltammetric measurements can be realized in a wide potential window. Presence of cadmium(II) allows to separate peaks of Hg(II) and Sb(III) and apparently catalyses reoxidation of electrolytically accumulated mercury, thus allowing its determination at ppb levels. Calibration dependence was linear up to 100 ppb Hg with a detection limit of 1.3 ppb. Applicability of the method was tested on the real river water sample.

  14. Anodic stripping tin titration: a method for the voltammetric determination of platinum at trace levels.

    Science.gov (United States)

    Giussani, Barbara; Roncoroni, Simone; Nemenyi, Anna; Dal Santo, Vladimiro; Monticelli, Damiano; Recchia, Sandro

    2014-07-01

    We propose here a novel voltammetric method for the determination of platinum at trace levels. The method is based on the interference that platinum generates on the anodic stripping signal of tin acidic solutions: in appropriate conditions platinum uses the intermediate formation of tin(II) ions, taking place during the tin cathodic reduction, to reduce itself and to form mixed Pt(II)-Sn(II) chloro-complexes. From the analysis of the anodic stripping plots obtained after subsequent additions of tin in a Pt-containing solution, it is possible to quantify accurately and precisely the Pt concentration from 3 ppb to more than 10 ppm. This novel method is validated for the analysis of Pt in heterogeneous catalysts, but in principle could be extended to other matrixes.

  15. Cathodic adsorptive stripping voltammetry of drotaverine hydrochloride and its determination in tablets and human urine by differential pulse voltammetry.

    Science.gov (United States)

    Zayed, S I M; Issa, Y M

    2009-04-01

    The stripping voltammetric behaviour of drotaverine hydrochloride (DvCl) was studied using a hanging mercury drop electrode (HMDE). The adsorptive stripping response has been evaluated with respect to pH, accumulation time, accumulation potential, scan rate and other variables. Differential pulse DP mode; over the potential range -400 to -1200 mV, is used in the presence of 0.04 M Britton-Robinson buffer pH 2. Cyclic voltammetric study indicates that the reduction process is irreversible and controlled by adsorption. The response of DP technique is linear over the concentration range 21.70-257.34 ng/ml. Limit of detection and limit of quantification were 3.15 and 10.50 ng/ml, respectively. The proposed method was successfully applied for the determination of the drug in commercial tablets and spiked human urine samples.

  16. Solar UV Photooxidation as Pretreatment for Stripping Voltammetric Trace Metal Analysis in River Water

    Directory of Open Access Journals (Sweden)

    Gelaneh Woldemichael

    2011-01-01

    Full Text Available The application of solar ultraviolet radiation as sample pretreatment or preparation step in stripping voltammetric analysis of trace metals in presence of low levels of dissolved organic carbon (DOC natural water samples (river water was studied. River water samples were collected from downstream of Warnow river (Germany and acidified to pH of 2±0.2 (by addition of 1 mL of ultrapure 65% HNO3 per liter sample. Furthermore, 100 μL/L of hydrogen peroxide solution (ultrapure, 30% H2O2 was added to the samples as photochemical reaction initiator. The samples were transferred to polyethylene terephthalate (PET bottles and irradiated with solar radiation of UV-A intensity of 3.6 mW/m2 for six hours, and the concentrations of Zn, Cd, Pb, and Cu were determined by differential pulse anodic stripping voltammetry (DPASV. The comparison of the values with the results obtained for the original untreated sample and artificial UV-treated one proved that solar UV radiation can be applied to the digestion of dissolved organic carbon in trace metal analysis in natural waters like river water, lake waters, well waters, and so forth.

  17. Construction and evaluation of a carbon paste electrode modified with polyaniline-co-poly(dithiodianiline) for enhanced stripping voltammetric determination of metal ions

    CSIR Research Space (South Africa)

    Somerset, V

    2014-05-01

    Full Text Available copolymer of polyaniline-co-poly(2,2'- dithiodianiline) (PANI-co-PDTDA) was used as a modified substrate transducer to achieve enhanced selectivity in stripping voltammetric analysis. The experimental conditions optimised included the supporting electrolyte...

  18. Cyclopentanone thiosemicarbazone, a new complexing agent for copper determination in biological samples by adsorptive stripping voltammetry.

    Science.gov (United States)

    Mahajan, Rakesh Kumar; Walia, T P S; Sumanjit; Lobana, T S

    2006-03-01

    A selective and sensitive stripping voltammetric method for the determination of trace amounts of copper(II) with cyclopentanone thiosemicarbazone (CPTSC) is presented. The method is based on the adsorptive accumulation of the resulting copper-CPTSC complex on a hanging mercury drop electrode, followed by the stripping voltammetric measurements at the reduction current of the adsorbed complex at -0.37 V vs. Ag/AgCl. The optimal conditions for the stripping analysis of copper include pH 9.3, deposition time of 120 s, and a deposition potential of -0.1 V (vs. Ag/AgCl). The peak current is linearly proportional to the copper concentration over a range 3.14 x 10(-9) M to 1.57 x 10(-6) M with a limit of detection of 1.57 x 10(-9) M. The technique has been applied to the determination of copper in biological samples, like urine and whole blood.

  19. Dual-nanomaterial based electrode for voltammetric stripping of trace Fe(II) in coastal waters.

    Science.gov (United States)

    Lin, Mingyue; Pan, Dawei; Zhu, Yun; Hu, Xueping; Han, Haitao; Wang, ChenChen

    2016-07-01

    In this work, a dual-nanomaterial based electrode was established for selective and sensitive detection of trace Fe(II) in the presence of complexing agent (2,2'-bipyridyl). Titanium carbide nanoparticles (TiCNPs) were used as the growth-template for the formation of three-dimensional platinum nanoflowers (PtNFs) due to their unique cubic structures. Nafion was employed as the conducting matrix to help TiCNPs better attached onto the surface of the electrode and slow down the crystal rate of PtNFs during electrodeposition, which resulted in flower structure and more active surface of PtNFs. Taking advantage of synergistic effects of TiCNPs and Nafion as well as the catalytic amplifying effect of PtNFs, the excellent anodic signal responses for the voltammetric stripping determination of Fe(II) were obtained. The linear range of Fe(II) on this dual-nanomaterial based electrode was from 1nmolL(-1) to 6μmolL(-1) with the lowest detectable concentration of 0.1nmolL(-1) and a detection limit of 0.03nmolL(-1). Additionally, the effect of several experimental parameters, such as concentration and pH value of buffer solution, concentration of modifier and ligand, deposition potential and time of electrochemical determination, and scan rate were studied for analytical applications. The fabricated sensor had been successfully applied for the sensitive determination of trace Fe(II) in coastal waters.

  20. Application of graphene for preconcentration and highly sensitive stripping voltammetric analysis of organophosphate pesticide

    Energy Technology Data Exchange (ETDEWEB)

    Wu Shuo, E-mail: wushuo@dlut.edu.cn [School of Chemistry, Dalian University of Technology, Dalian 116023 (China); Lan Xiaoqin; Cui Lijun; Zhang Lihui; Tao Shengyang; Wang Hainan; Han Mei; Liu Zhiguang; Meng Changgong [School of Chemistry, Dalian University of Technology, Dalian 116023 (China)

    2011-08-12

    Highlights: {yields} An electrochemical sensor is fabricated based on {beta}-CD dispersed graphene. {yields} The sensor could selectively detect organophosphate pesticide with high sensitivity. {yields} The {beta}-CD dispersed graphene owns large adsorption capacity for MP and superconductivity. {yields} The {beta}-CD dispersed graphene is superior to most of the porous sorbents ever known. - Abstract: Electrochemical reduced {beta}-cyclodextrin dispersed graphene ({beta}-CD-graphene) was developed as a sorbent for the preconcentration and electrochemical sensing of methyl parathion (MP), a representative nitroaromatic organophosphate pesticide with good redox activity. Benefited from the ultra-large surface area, large delocalized {pi}-electron system and the superconductivity of {beta}-CD-graphene, large amount of MP could be extracted on {beta}-CD-graphene modified electrode via strong {pi}-{pi} interaction and exhibited fast accumulation and electron transfer rate. Combined with differential pulse voltammetric analysis, the sensor shows ultra-high sensitivity, good selectivity and fast response. The limit of detection of 0.05 ppb is more than 10 times lower than those obtained from other sorbent based sensors. The method may open up a new possibility for the widespread use of electrochemical sensors for monitoring of ultra-trace OPs.

  1. Stripping voltammetric determination of palladium, platinum and rhodium in freshwater and sediment samples from South African water resources

    CSIR Research Space (South Africa)

    Van der Horst, C

    2012-08-01

    Full Text Available of platinum (Pt2+), palladium (Pd2+) or rhodium (Rh2+) by means of adsorptive cathodic stripping voltammetry. Optimised experimental conditions included composition of the supporting electrolyte, complexing agent concentration, deposition potential, deposition...

  2. A validated stripping voltammetric procedure for quantification of the anti-hypertensive and benign prostatic hyperplasia drug terazosin in tablets and human serum.

    Science.gov (United States)

    Ghoneim, M M; El Ries, M A; Hammam, E; Beltagi, A M

    2004-10-20

    The electrochemical behavior of terazosin at the hanging mercury drop electrode was studied in Britton-Robinson buffer (pH 2-11), acetate buffer (4.5-5.5), and in 0.1M solution of each of sodium sulfate, sodium nitrate, sodium perchlorate and potassium chloride as supporting electrolytes. The square-wave adsorptive cathodic stripping voltammogram of terazosin exhibited a single well-defined two-electron irreversible cathodic peak which may be attributed to the reduction of CO double bond of the drug molecule. A fully validated, simple, high sensitive, precise and inexpensive square-wave adsorptive cathodic stripping voltammetric procedure was described for determination of terazosin in bulk form, tablets and human serum. A mean recovery for 1x10(-8)M terazosin in bulk form, following preconcentration onto the hanging mercury drop electrode for 60s at a -1.0V (versus Ag/AgCl/KCl(s)), of 99+/-0.7% (n=5) was obtained. Limits of detection (LOD) and quantitation (LOQ) of 1.5x10(-11) and 5x10(-11)M bulk terazosin were achieved, respectively. The proposed procedure was successfully applied to determination of the drug in its Itrin((R)) tablets and human serum samples. The achieved LOD and LOQ of the drug in human serum samples were 5.3x10(-11) and 1.8x10(-10)M THD, respectively. The pharmacokinetic parameters of the drug in human plasma were estimated as: C(max)=77.5ngml(-1), t(max)=1.75h, AUC(0-t)=602.3nghml(-1), K(e)=0.088h(-1) and t(1/2)=11.32h) which are favorably compared with those reported in literature.

  3. Selective determination of trace copper(II) by cathodic adsorptive stripping voltammetry with a naphthol-derivative Schiff's base.

    Science.gov (United States)

    Shamsipur, Mojtaba; Saeidi, Mahboubeh; Sharghi, Hashem; Naeimi, Hossein

    2003-01-01

    A selective and sensitive stripping voltammetric method for the determination of trace amounts of copper(II) with a recently synthesized naphthol-derivative Schiff's base (2,2'-[1,2-ethanediylbis(nitriloethylidyne)]bis(1-naphthalene)) is presented. The method is based on adsorptive accumulation of the resulting copper-Schiff's base complex on a hanging mercury drop electrode, followed by the stripping voltammetric measurement at the reduction current of adsorbed complex at -0.15 V (vs. Ag/AgCl). The optimal conditions for the stripping analysis of copper include pH 5.5 to 6.5, 8 microM Schiff's base and an accumulation potential of -0.05 V (vs. Ag/AgCI). The peak current is linearly proportional to the copper concentration over a range 2.3-50.8 ng ml(-1) with a limit of detection of 1.9 ng ml(-1). The accumulation time and RSD are 90 s and (3.2-3.5)%, respectively. The method was applied to the determination of copper in some analytical grade salts, tap water, human serum and sheep's liver.

  4. Adsorptive stripping voltammetry of nickel with 1-nitroso-2-napthol using a bismuth film electrode.

    Science.gov (United States)

    Segura, Rodrigo; Pradena, Milenco; Pinto, Deny; Godoy, Fernando; Nagles, Edgar; Arancibia, Verónica

    2011-10-15

    A sensitive procedure is presented for the voltammetric determination of nickel. The procedure involves an adsorptive accumulation of nickel 1-nitroso-2-napthol (NN) complex on a bismuth film electrode prepared ex situ by electrodeposition. The most suitable operating conditions and parameters such as pH, ligand concentration (C(NN)), adsorptive potential (E(ads)), adsorptive time (t(ads)), scan rate and others were selected and the determination of nickel in aqueous solutions using the standard addition method was possible. The adsorbed Ni-NN complex gives a well defined cathodic stripping peak current at -0.70 V, which was used for the determination of nickel in the concentration range of 10.0-70.0 μg L(-1) (pH 7.5; C(NN) 6.5 μmol L(-1); E(ads) -0.30 V; t(ads) 60s) with a detection limit of 0.1 μg L(-1). The relative standard deviation for a solution containing 10.0 μg L(-1) of Ni(II) was 3.5% (n=4). The proposed method was validated determining Ni(II) in certified reference waste water (SPS-WW1) and Certified Reference Water for Trace Elements (TMDA 51.3) with satisfactory results. Then lake water samples were analyzed. Copyright © 2011. Published by Elsevier B.V.

  5. Solar UV-treatment of water samples for stripping-voltammetric determination of trace heavy metals in Awash river, Ethiopia

    Directory of Open Access Journals (Sweden)

    Gelaneh Woldemichael

    2016-03-01

    Full Text Available We report about testing a new mobile and sustainable water sample digestion method in a preliminary field trial in Ethiopia. In order to determine heavy metals at the ultra-trace level by stripping voltammetric techniques in water samples from Awash River, we applied our new method of solar UV-assisted sample pretreatment to destroy the relevant interfering dissolved organic matter. The field tests revealed that 24 h of solar UV irradiation were sufficient to achieve the same sample pretreatment results as with classic digestion method based on intense and hard UV. Analytical results of this study suggest that both a hydroelectric power station and agrichemical applications at Koka Lake have increased the levels of the investigated metals zinc, cadmium, lead, copper, cobalt, nickel, and uranium.

  6. Stripping voltammetric determination of Cd(Ⅱ) based on multiwalled carbon nanotube functionalized with 1-(2-pyridylazo)-2-naphthol

    Institute of Scientific and Technical Information of China (English)

    Alireza Mohadesi; Hadi Beitollahi; Mohammad Ali Karimi

    2011-01-01

    The present work has focused on the modification of multiwalled carbon nanotube with a ligand, l-(2-pyridylazo)-2-naphthol, and its potential application for the development of a new, simple and selective modified glassy carbon electrode for stripping voltammetric determination of Cd(Ⅱ). The analytical curve for Cd(Ⅱ) ions covered the linear range varying from 0.8 up to 220.4 μg L-1. The limit of detection was found to be 0.1 μg L-1, while the relative standard deviation (RSD) at 50.0 μg L-1 was 1.8% (n = 5). This modified electrode was successfully applied for determination of Cd(Ⅱ) in some water samples.

  7. Determination of trace amounts of thallium by adsorptive cathodic stripping voltammetry with xylenol orange.

    Science.gov (United States)

    Shams, Esmaeil; Yekehtaz, Mehdi

    2002-09-01

    Trace amounts of thallium(I) can be determined using adsorptive cathodic stripping voltammetry in the presence of Xylenol Orange (XO). The reduction current of the thallium(I)-XO complex ion was measured by square-wave cathodic stripping voltammetry. The peak potential was at -0.44 V vs. Ag/AgCl. The effect of various parameters (pH, ligand concentration, accumulation potential and collection time) on the response are discussed. The response was linearly related to the thallium concentration in the range 0.5-110 ng ml(-1) and 110-2000 ng ml(-1). The limit of detection was 0.2 ng ml(-1). The relative standard deviation for the determination of 80 ng ml(-1) thallium was 2.8%. Many common anions and cations did not interfere with the determination of thallium. The interference of lead was reduced by the addition of 0.003 M sodium carbonate. The voltammetric procedure was then successfully applied to the determination of thallium in various complex samples.

  8. Square-wave adsorptive cathodic stripping voltammetry of pantoprazole.

    Science.gov (United States)

    Radi, A

    2003-11-24

    Adsorption and reduction of pantoprazole were investigated by cyclic and square-wave voltammetry on a hanging mercury drop electrode in Britton-Robinson buffers at pH 2.0-11.0. The reduction process gave rise to a single peak within the entire pH range. Study of the variation of the reduction signal with solution variables such as pH and concentration of pantoprazole and instrumental variables such as accumulation time and potential, frequency, pulse height and pulse amplitude, has resulted in optimization of the reduction signal for analytical purposes. The voltammetric procedure was applied successfully to give a rapid and precise assay of pantoprazole in a tablet dosage form.

  9. Construction and evaluation of a carbon paste electrode modified with polyaniline-co-poly(dithiodianiline) for enhanced stripping voltammetric determination of metal ions

    OpenAIRE

    Somerset, Vernon; Silwana, Bongiwe; Horst, Charlton van der; Iwuoha, Emmanuel

    2014-01-01

    A modified carbon paste electrodes (MCPE) have been prepared in this study as an alternative “mercury-free” electrochemical sensor for the determination of Pb2+ and Cd2+ metal ions in aqueous solutions. CPE containing a conducting copolymer of polyaniline-co-poly(2,2'- dithiodianiline) (PANI-co-PDTDA) was used as a modified substrate transducer to achieve enhanced selectivity in stripping voltammetric analysis. The experimental conditions optimised included the supporting electrolyte pH, d...

  10. Electrochemical behavior of folic acid at calixarene based chemically modified electrodes and its determination by adsorptive stripping voltammetry

    Energy Technology Data Exchange (ETDEWEB)

    Vaze, Vishwanath D. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India); Srivastava, Ashwini K. [Department of Chemistry, University of Mumbai, Vidyanagari, Santacruz (East), Mumbai 400098 (India)], E-mail: aksrivastava@chem.mu.ac.in

    2007-12-31

    Voltammetric behavior of folic acid at plain carbon paste electrode and electrode modified with calixarenes has been studied. Two peaks for irreversible oxidation were observed. Out of the three calixarenes chosen for modification of the electrodes, p-tert-butyl-calix[6]arene modified electrode (CME-6) was found to have better sensitivity for folic acid. Chronocoulometric and differential pulse voltammetric studies reveal that folic acid can assemble at CME-6 to form a monolayer whose electron transfer rate is 0.00273 s{sup -1} with 2-electron/2-proton transfer for the peak at +0.71 V against SCE. An adsorption equilibrium constant of 5 x 10{sup 3} l/mol for maximum surface coverage of 2.89 x 10{sup -10} mol/cm{sup 2} was obtained. The current is found to be rectilinear with concentration by differential pulse voltammetry. However, linearity in the lower range of concentration 8.79 x 10{sup -12} M to 1.93 x 10{sup -9} M with correlation coefficient of 0.9920 was achieved by adsorptive stripping voltammetry. The limit of detection obtained was found to be 1.24 x 10{sup -12} M. This method was used for the determination of folic acid in a variety of samples, viz. serum, asparagus, spinach, oranges and multivitamin preparations.

  11. Stripping Voltammetric Determination of Analgesics in Their Pharmaceuticals Using Nano-Riboflavin-Modified Glassy Carbon Electrode

    Directory of Open Access Journals (Sweden)

    Gopalakrishnan Gopu

    2011-01-01

    Full Text Available Cyclic voltammetric behaviors of three analgesics, acetaminophen (AAP, acetylsalicylic acid (ASA, and dipyrone (DP, were studied using nano-riboflavin-modified glassy carbon electrode. One well-defined oxidation peak each for AAP and ASA and three oxidation peaks for DP were observed. The influence of pH, scan rate, and concentration reveals irreversible diffusion controlled reaction. The SEM analysis confirmed good accumulation of the drugs on the electrode surface. Calibration was made under the maximum peak current conditions. The concentration range studied for the determination of drugs was 0.02 to 0.4 μg mL−1 for AAP and ASA and 0.025 to 0.4 μg mL−1 for DP. The lower limit of detection observed for AAP, ASA, and DP was 0.016, 0.007 μg mL−1, and 0.013 μg mL−1, respectively. The suitability of the method for the determination of these analgesics in pharmaceutical preparations and urine samples was also ascertained.

  12. Electrochemical determination of closantel in the commercial formulation by square-wave adsorptive stripping voltammetry.

    Science.gov (United States)

    Brycht, Mariola; Nosal-Wiercińska, Agnieszka; Sipa, Karolina; Rudnicki, Konrad; Skrzypek, Sławomira

    2017-01-01

    In this paper, the square-wave adsorptive stripping voltammetric (SWAdSV) determination of the veterinary drug closantel using a renewable silver amalgam film electrode (Hg(Ag)FE) is presented. As observed in SWAdSV, closantel provided one well-shaped reduction peak suitable for analytical purposes at potential ca. -1.4 V in the Britton-Robinson (B-R) buffer at pH 7.0. At optimal conditions, the SWAdSV response of Hg(Ag)FE for determining closantel was linear over two concentration ranges of 5.0 × 10(-8) to 2.0 × 10(-7) mol dm(-3) and 2.0 × 10(-7) to 1.2 × 10(-6) mol dm(-3) with a detection limit of 1.1 × 10(-8) mol dm(-3). In addition, a relevance of the developed SWAdSV method was successfully verified by the quantitative analysis of closantel in the commercial formulation Closamectin Pour-On with satisfactory results (RSD = 5.8%, recovery = 101.8%). The results showed that the developed procedure can be adequate for screening purposes. Also, the electrochemical behavior of closantel was characterized by cyclic voltammetry, and it was found that closantel exhibited a quasi-reversible behavior with cathodic peak on the forward scan at ca. -1.4 V and anodic peak on the reverse scan at ca. -1.35 V vs. Ag/AgCl in B-R buffer, pH 7.0. As the obtained results showed that the electrode mechanism of closantel is controlled by the adsorption, the effect of adsorption was studied using the electrochemical impedance spectroscopy technique.

  13. Detecting Naturally-Produced Sulfide Nanoparticles by Adsorptive, Cathodic Stripping Voltammetry.

    Science.gov (United States)

    Helz, G. R.; Krznaric, D.; Bura-Nakic, E.; Ciglenecki, I.

    2007-12-01

    Growing evidence implies that metal sulfide nanoparticles of natural origin exist in some aquatic environments. These nanoparticles could play important roles as mediators of trace metal nutrition and toxicity. Thermodynamics suggests that in sulfidic environments (total transition metaltotal sulfide) the most insoluble metal sulfide (usually Hg or Cu) will form the predominant sulfide nanoparticle. New experimental methods for detecting and distinguishing between such nanoparticles are needed. We report that mercury electrodes effectively preconcentrate a number of different metal sulfide nanoparticles, enabling their detection by adsorptive cathodic stripping voltammetry. Voltammetrically, nanoparticulate analytes differ fundamentally from dissolved analytes; e.g. analyte accumulation is very sensitive to electrolyte composition and concentration in accord with the Schulze-Hardy Rule. EDTA or acid treatment of samples is useful for distinguishing highly insoluble nanoparticles (HgS, CuS) from FeS. Nanoparticulate sulfur potentially interferes. Supersaturated solutions can generate artifactual analyte on Hg electrode surfaces. Despite such potential pitfalls, progress is encouraging. Preliminary, qualitative results from natural waters will be reported.

  14. Advantages of using a mercury coated, micro-wire, electrode in adsorptive cathodic stripping voltammetry.

    Science.gov (United States)

    Gun, Jenny; Salaün, Pascal; van den Berg, Constant M G

    2006-06-30

    A mercury coated, gold, micro-wire electrode is used here for the determination of iron in seawater by catalytic cathodic stripping voltammetry (CSV) with a limit of detection of 0.1 nM Fe at a 60s adsorption time. It was found that the electrode surface is stable for extended periods of analyses (at least five days) and that it is reactivated by briefly (2s) applying a negative potential prior to each scan. Advantages of this electrode over mercury drop electrodes are that metallic mercury use is eliminated and that it can be readily used for flow analysis. This is demonstrated here by the determination of iron in seawater by continuous flow analysis. It is likely that this method can be extended to other elements. Experiments using bismuth coated, carbon fibre, electrodes showed that the bismuth catalyses the oxidation of the important oxidants bromate and hydrogen peroxide, which makes it impossible to use bismuth based electrodes for catalytic CSV involving these oxidants. For this reason mercury coated electrodes retain a major advantage for catalytic voltammetric analyses.

  15. Polarographic behaviour of loratadine and its direct determination in pharmaceutical formulation and human plasma by cathodic adsorptive stripping voltammetry.

    Science.gov (United States)

    Ghoneim, M M; Mabrouk, M M; Hassanein, A M; Tawfik, A

    2001-07-01

    The polarographic behaviour of the antihistaminic drug loratadine has been investigated in B.R. buffer solution of different pH values. Contradictory to that mentioned before in a previously published work, loratadine is electro-active at the mercury electrode. In B.R. buffer solution of pH values > or =6 it is reduced via a single 2-electrons irreversible wave corresponding to saturation of carbon-nitrogen double bond of the pyridine ring. The electrode reaction pathway was proposed and discussed. A sensitive differential pulse stripping voltammetric method based on controlled adsorptive accumulation of loratadine on a hanging mercury drop electrode has been developed for its direct determination at nanomolar concentrations without nitration of the drug. The optimized conditions for the direct cathodic adsorptive stripping voltammetric determination of the drug are: 0.1 M sodium hydroxide solution as a supporting electrolyte, accumulation potential, -1.2 V; accumulation time, 30 s; scan rate, 2-5 mV x s(-1) and pulse amplitude 100 mV. The proposed procedure was applied for the assay of loratadine in pharmaceutical formulation and human plasma. The average recoveries were 99.32-99.44 and 100.33-102.99% with the RSD 0.27-0.42 and 0.39-0.90% in pharmaceutical formulation and human plasma, respectively. The limits of detection of 1.60x10(-7) and 1.25x10(-7) M loratadine were found in pharmaceutical formulation and human plasma, respectively.

  16. Cathodic stripping voltammetric determination of arsenic in sugarcane brandy at a modified carbon nanotube paste electrode.

    Science.gov (United States)

    Teixeira, Meryene C; Tavares, Elisângela de F L; Saczk, Adelir A; Okumura, Leonardo L; Cardoso, Maria das Graças; Magriotis, Zuy M; de Oliveira, Marcelo F

    2014-07-01

    We have developed an eletroanalytical method that employs Cu(2+) solutions to determine arsenic in sugarcane brandy using an electrode consisting of carbon paste modified with carbon nanotubes (CNTPE) and polymeric resins. We used linear sweep (LSV) and differential-pulse (DPV) voltammetry with cathodic stripping for CNTPE containing mineral oil or silicone as binder. The analytical curves were linear from 30 to 110μgL(-1) and from 10 to 110μgL(-1) for LSV and DPV, respectively. The limits of detection (L.O.D.) and quantification (L.O.Q.) of CNTPE were 10.3 and 34.5μgL(-1) for mineral oil and 3.4 and 11.2μgL(-1) for silicone. We applied this method to determine arsenic in five commercial sugarcane brandy samples. The results agreed well with those obtained by hydride generation combined with atomic absorption spectrometry (HG AAS).

  17. Speciation study of aluminium in beverages by Competitive Ligand Exchange-Adsorptive Stripping Voltammetry.

    Science.gov (United States)

    Magnier, A; Fekete, V; Van Loco, J; Bolle, F; Elskens, M

    2014-05-01

    Competitive Ligand Exchange-Adsorptive Stripping Voltammetry (CLE-AdSV) was used for determining the speciation of aluminium in commonly consumed beverages (water, tea, infusion, coffee, orange juice, tomato juice, beer and red wine). Aluminium determination involves the adsorption of Al-complexes with the ligand cupferron onto a hanging mercury drop electrode. All samples were studied at pH 6.5 with an accumulation step at -0.60 V (all potential values in the paper are given versus the Ag/AgCl, [KCl]=3 M reference electrode) during 60 s, and a final cupferron concentration of 4 × 10(-4)M. These conditions were used to establish (i) the concentration of electro-labile aluminium, (ii) the range of ligand concentrations and (iii) the conditional stability constants of beverage samples using titration procedures. The results based on Ruzic plots were compared to computer simulation with Visual MINTEQ. This comparison suggests that labile monomeric Al-forms and soluble organic complexes of low molecular weight can be quantified by the CLE-AdSV procedure. Overall the relative uncertainties on the determination of the electro-active Al fraction and the complexing parameters, i.e., concentration and conditional stability constant of natural ligands in the samples, are less than 15%. Thanks to these results, information on Al bioavailability in beverages was collected and discussed. This study also illustrates the value of computer simulations when complex, time-consuming voltammetric techniques are applied. Copyright © 2014 Elsevier B.V. All rights reserved.

  18. Copper-mercury film electrode for cathodic stripping voltammetric determination of Se(IV).

    Science.gov (United States)

    Sladkov, Vladimir; David, François; Fourest, Blandine

    2003-01-01

    The copper-mercury film electrode has been suggested for the determination of Se(IV) in a wide range of concentration from 1x10(-9) to 1x10(-6) mol L(-1)by square-wave cathodic stripping voltammetry. Insufficient reproducibility and sensitivity of the mercury film electrode have been overcome by using copper(II) ions during the plating procedure. Copper(II) has been found to be reduced and form a reproducible copper-mercury film on a glassy carbon electrode surface. The plating potential and time, the concentration of copper(II) and the concentration of the supporting electrolyte have been optimised. Microscopy has been used for a study of the morphology of the copper-mercury film. It has been found that it is the same as for the mercury one. The preconcentration step consists in electrodeposition of copper selenide on the copper-mercury film. The relative standard deviation is 4.3% for 1x10(-6) mol L(-1) of Se(IV). The limit of detection is 8x10(-10) mol L(-1) for 5 min of accumulation.

  19. Differential Pulse Anodic Stripping Voltammetric Determination of Lead with Heparin Modified Electrode

    Institute of Scientific and Technical Information of China (English)

    LI,Nian-Bing(李念兵); DUAN,Jian-Ping(段建平); CHEN,Guo-Nan(陈国南)

    2004-01-01

    A novel differential pulse anodic stripping voltammetry for the determination of trace amounts of lead, using a biomacromolecule heparin drop-coated modified glassy carbon electrode, has been described. Pb2+ was deposited on the surface of a heparin-modified electrode at - 1.0 V (vs. SCE) via forming Pb2+-heparin and subsequent reduction at the electrode. In the following step, Pb-heparin was oxidized, and voltammograms were recorded by scanning the potential in a positive direction. Conditions were optimized with respect to the pH of the medium, the mass of drop-coated heparin, accumulation potential and accumulation time. The peak current was proportional to the Pb2+ concentration in the range of 2.0× 10-9 to 7.0× 10-7 mol/L, The detection limit was 3.0× 10-10 mol/L.The relative standard deviation was 4.83% for 1.0× 10-8mol/L Pb2- (n= 10). The developed method has been applied to the determination of Pb2- in water samples with satisfactory results.

  20. Electrochemical determination of resveratrol in dietary supplements at a boron-doped diamond electrode in the presence of hexadecyltrimethylammonium bromide using square-wave adsorptive stripping voltammetry

    Directory of Open Access Journals (Sweden)

    Yardim Yavuz

    2017-01-01

    Full Text Available A sensitive electroanalytical methodology for the determination of resveratrol is presented for the first time using adsorptive stripping voltammetry at a bare boron-doped diamond (BDD electrode. In cyclic voltammetry, resveratrol shows one irreversible and an adsorption-controlled oxidation peak at a BDD electrode. The voltammetric results indicated that in the presence of hexadecyl trimethyl ammonium bromide, the BDD electrode remarkably enhanced the oxidation of resveratrol, which leads to an improvement in the peak current with a shift of the peak potential to more positive values. Using the square-wave stripping mode, the compound yielded a well-defined voltammetric response in 0.1 M nitric acid solution containing 100 μmol L-1 hexadecyl trimethyl ammonium bromide at 0.74 V (vs. Ag/AgCl, after 60 s accumulation at the open-circuit condition. A linear calibration graph was obtained in the concentration range 0.025 to 60.0 μg mL-1, with a detection limit of 0.0063 μg mL-1. The applicability of the proposed method was verified by analysis of resveratrol in commercial dietary supplements.

  1. Determination of tryptamine in foods using square wave adsorptive stripping voltammetry.

    Science.gov (United States)

    Costa, Daniel J E; Martínez, Ana M; Ribeiro, Williame F; Bichinho, Kátia M; Di Nezio, María Susana; Pistonesi, Marcelo F; Araujo, Mario C U

    2016-07-01

    Tryptamine, a biogenic amine, is an indole derivative with an electrophilic substituent at the C3 position of the pyrrole ring of the indole moiety. The electrochemical oxidation of tryptamine was investigated using glassy carbon electrode (GCE), and focusing on trace level determination in food products by square wave adsorptive stripping voltammetry (SWAdSV). The electrochemical responses of tryptamine were evaluated using differing voltammetric techniques over a wide pH range, a quasi-reversible electron-transfer to redox system represented by coupled peaks P1-P3, and an irreversible reaction for peak P2 were demonstrated. The proton and electron counts associated with the oxidation reactions were estimated. The nature of the mass transfer process was predominantly diffusion-limited for the oxidation process of P1, the most selective and sensitive analytical response (acetate buffer solution pH 5.3), being used for the development of SWAdSV method, under optimum conditions. The excellent response allowed the development of an electroanalytical method with a linear response range of from 4.7-54.5)×10(-)(8)molL(-1), low detection limit (0.8×10(-)(9)molL(-)(1)), and quantification limit (2.7×10(-9)molL(-1)), and acceptable levels of repeatability (3.6%), and reproducibility (3.8%). Tryptamine content was determined in bananas, tomatoes, cheese (mozzarella and gorgonzola), and cold meats (chicken sausage and pepperoni sausage), yielding recoveries above 90%, with excellent analytical performance using simple and low cost instrumentation.

  2. Determination of vanillin in commercial food product by adsorptive stripping voltammetry using a boron-doped diamond electrode.

    Science.gov (United States)

    Yardım, Yavuz; Gülcan, Mehmet; Şentürk, Zühre

    2013-12-01

    A method for the determination of food additive vanillin was developed by adsorptive stripping voltammetry. Its determination was carried out at the anodically pre-treated boron-doped diamond electrode in aqueous solutions. Using square-wave stripping mode, the compound yielded a well-defined voltammetric response in phosphate buffer, pH 2.5 at +1.14 V (vs. Ag/AgCl) (a pre-concentration step being carried out at open-circuit condition for 60s). A linear calibration graph was obtained in the concentration range of 0.5-15.0 μg mL(-1) (3.3×10(-6)-9.8×10(-5) mol L(-1)) with a detection limit of 0.024 μg mL(-1) (1.6×10(-7) mol L(-1)). As an example, the practical applicability of the proposed method was tested for the determination of this flavouring agent in commercial pudding powder of Keshkule (Turkish milk pudding with almond flour).

  3. Differential pulse cathodic stripping voltammetric determination of uranium with arsenazo-III at the hanging mercury dropping electrode

    Energy Technology Data Exchange (ETDEWEB)

    Kadi, M.W.; El-Shahawi, M.S. [Chemistry Dept., King Abdulaziz Univ., Jeddah (Saudi Arabia)

    2009-07-01

    An accurate, inexpensive and less laborious controlled adsorptive accumulation of uranium(VI)-arsenazo-III on a hanging mercury drop electrode (HMDE) has been developed for uranium(VI) determination. The method is based upon the collection of uranium(VI)-arsenazo-III complex at pH 5-6 at the HMDE and subsequent direct stripping measurement of the element in the nanomolar concentration level. The cathodic peak current (i{sub p,c}) of the adsorbed complex ions of uranium(VI) was measured at -0.35 V vs. Ag/AgCl reference electrode by differential pulse cathodic stripping voltammetry (DP-CSV), proceeded by an accumulation period of 150s2.5 in Britton-Robinson buffer of pH 5. The plot of the resulting i{sub p,c} vs. uranium(VI) concentration was linear in the range 2.1 x 10{sup -9} to 9.60 x 10{sup -7} mol L{sup -1} uranium(VI) and tended to level off at above 9.6 x 10{sup -7} mol L{sup -1}. The limits of detection and quantification of uranium(VI) were found to be 4.7 x 10{sup -10} and 1.5 x 10{sup -9} mol L{sup -1}, respectively. A relative standard deviation of {+-}2.39% (n = 5) at 8.5 x 10{sup -7} mol L{sup -1} uranium(VI) was obtained. The method was validated by comparing the results with that obtained by ICP-MS method with RSD less than {+-}3.3%. The method was applied successfully for the analysis of uranium in certified reference material (IAEA soil-7), and in phosphate fertilizers. (orig.)

  4. A study of the determination of the hypertensive drug captopril by square wave cathodic adsorptive stripping voltammetry.

    Science.gov (United States)

    Ioannides, X; Economou, A; Voulgaropoulos, A

    2003-09-19

    In this work, the determination of captopril (CPL) was studied by square wave cathodic adsorptive stripping voltammetry (SWCAdSV) on a hanging mercury drop electrode (HMDE). CPL was adsorptively preconcentrated on the mercury surface as a sparingly soluble mercury salt under stirring of the solution and then the accumulated species was reduced by a cathodic square wave voltammetric scan. The reduction current was related to the CPL concentration in the sample. The chemical and instrumental parameters affecting the response were investigated and optimized for the CPL determination. The calibration curve was linear from 0.5 to 180 microg l(-1) of CPL (depending on the preconcentration time), the limit of detection at a S/N ratio of 3 was 0.5 microg l(-1) with 300 s of preconcentration and the relative standard deviation was 3.2% at the 20 microg l(-1) level (with 120 s of preconcentration, n=8). The method was applied to the determination of CPL in two pharmaceutical formulations with recoveries of 97.9 and 98.8%. Finally, the potential for applying the proposed method to the determination of CPL in biological media is briefly discussed.

  5. Novel acyclonucleoside analog bearing a 1,2,4-triazole–Schiff base: Synthesis, characterization and analytical studies using square wave-adsorptive stripping voltammetry and HPLC

    Directory of Open Access Journals (Sweden)

    Ali F. Alghamdi

    2017-09-01

    Full Text Available New acyclonucleoside analogs tethered by a 1,2,4-triazole scaffold were synthesized through the condensation of 4-amino-5-(2-phenyleth-1-yl-2,4-dihydro-3H-1,2,4-triazole-3-thione (2 with benzaldehyde followed by the alkylation of the resulting Schiff base (3with 2-bromoethanol, 3-chloropropanol and/or 3-chloropropan-1,2-diol. Voltammetric studies were carried out for the analysis of 1 × 10−6 mol L−1 of the newly synthesized acyclonucleoside analogs (4–6 using square wave-adsorptive stripping voltammetry (SW-AdSV. The sharp voltammetric peak and high reduction current were recorded using a Britton–Robinson B–R pH 10 buffer at Ep = −1250 mV on the hanging mercury drop surface (HMDE and Ag/AgCl reference electrode. Several experimental conditions were studied, such as the supporting electrolytes, the pH, and the accumulation time, as well as the potential, the scan rate, the frequency and the step potential for 4-benzylideneamino-5-(2-phenyleth-1-yl-3-[(2,3-dihydroxyprop-1-ylthio]-1,2,4-triazole (6. The analytical performance of the voltammetric technique was investigated through the analysis of the calibration curve, the detection limit, the recovery and the stability. The voltammetric analytical applications were evaluated by the recovery of compound (6 in the urine and plasma samples. The HPLC technique was also applied for the separation of compound (6 from interference using a C-18 (5 μm column with UV detection at 254 nm.

  6. Adsorptive stripping voltammetric study of vitamin B1 at multi-walled carbon nanotube paste electrode

    Directory of Open Access Journals (Sweden)

    Pradeep Kumar Brahman

    2016-11-01

    The reduction peak current varies linearly with the concentration of vitamin B1 over the range of 1.0 × 10−7–1.0 × 10−6 M. The limits of detection and quantification of the pure drug are 1.1 × 10−10 M and 2.0 × 10−9 M, with the correlation coefficient, r = 0.997 and the relative standard deviation, RSD = 1.2% (n = 5. Experimental results reveal that the MWCNTPE has advantages of small background current, high signal to background current ratio and good reproducibility.

  7. Optimization of Stripping Voltammetric Sensor by a Back Propagation Artificial Neural Network for the Accurate Determination of Pb(II) in the Presence of Cd(II).

    Science.gov (United States)

    Zhao, Guo; Wang, Hui; Liu, Gang; Wang, Zhiqiang

    2016-09-21

    An easy, but effective, method has been proposed to detect and quantify the Pb(II) in the presence of Cd(II) based on a Bi/glassy carbon electrode (Bi/GCE) with the combination of a back propagation artificial neural network (BP-ANN) and square wave anodic stripping voltammetry (SWASV) without further electrode modification. The effects of Cd(II) in different concentrations on stripping responses of Pb(II) was studied. The results indicate that the presence of Cd(II) will reduce the prediction precision of a direct calibration model. Therefore, a two-input and one-output BP-ANN was built for the optimization of a stripping voltammetric sensor, which considering the combined effects of Cd(II) and Pb(II) on the SWASV detection of Pb(II) and establishing the nonlinear relationship between the stripping peak currents of Pb(II) and Cd(II) and the concentration of Pb(II). The key parameters of the BP-ANN and the factors affecting the SWASV detection of Pb(II) were optimized. The prediction performance of direct calibration model and BP-ANN model were tested with regard to the mean absolute error (MAE), root mean square error (RMSE), average relative error (ARE), and correlation coefficient. The results proved that the BP-ANN model exhibited higher prediction accuracy than the direct calibration model. Finally, a real samples analysis was performed to determine trace Pb(II) in some soil specimens with satisfactory results.

  8. Trace and selective determination of cobalt(II in water and salt samples using cathodic adsorptive stripping voltammetry in the presence of pyrogallol red

    Directory of Open Access Journals (Sweden)

    Hasanpour Foroozan

    2013-01-01

    Full Text Available A sensitive and selective procedure is presented for voltammetric determination of cobalt. The procedure involves an adsorptive accumulation of cobalt pyrogallol red (PGR complex on stationary mercury drop electrode, followed by cathodic stripping voltammetry measurement of reduction current of adsorbed complex at -1.17 V (vs. Ag/AgCl. The optimum conditions for determination of cobalt include pH 11.0, 35 μM pyrogallol red, an accumulation potential of -0.9 V (vs. Ag/AgCl and scan rate 80 mVs-1. The peak current is proportional to the concentration of cobalt over the concentration range of 5.0 to 280 ng mL-1 with a detection limit of 1 ng mL-1 with an accumulation time of 140 s. The method was applied for the determination of cobalt in analytical grade NaCl and water samples.

  9. Determination of Xanthine in the Presence of Hypoxanthine by Adsorptive Stripping Voltammetry at the Mercury Film Electrode

    Science.gov (United States)

    Farias, Percio Augusto Mardini; Castro, Arnaldo Aguiar

    2014-01-01

    A stripping method for the determination of xanthine in the presence of hypoxanthine at the submicromolar concentration levels is described. The method is based on controlled adsorptive accumulation at the thin-film mercury electrode followed by a fast linear scan voltammetric measurement of the surface species. Optimum experimental conditions were found to be the use of 1.0 × 10−3 mol L−1 NaOH solution as supporting electrolyte, an accumulation potential of 0.00 V for xanthine and −0.50 V for hypoxanthine–copper, and a linear scan rate of 200 mV second−1. The response of xanthine is linear over the concentration ranges of 20–140 ppb. For an accumulation time of 30 minutes, the detection limit was found to be 36 ppt (2.3 × 10−10 mol L−1). Adequate conditions for measuring the xanthine in the presence of hypoxanthine, copper and other metals, uric acid, and other nitrogenated bases were also investigated. The utility of the method is demonstrated by the presence of xanthine associated with hypoxanthine, uric acid, nitrogenated bases, ATP, and ssDNA. PMID:24940040

  10. Determination of the antibiotic drug pefloxacin in bulk form, tablets and human serum using square wave cathodic adsorptive stripping voltammetry.

    Science.gov (United States)

    Beltagi, A M

    2003-04-10

    A simple, rapid, reliable and fully validated square wave cathodic adsorptive stripping voltammetric procedure has been developed for the determination of the antibiotic pefloxacin drug in bulk form, tablets and human serum, based on its electrochemical reduction at a hanging mercury drop electrode. The Britton-Robinson buffer of pH 7.0 was found to be reasonable as a supporting electrolyte for assay of the drug. Pefloxacin drug, at the optimized conditions, showed a single 2-electron well-defined peak at -1.07 V (versus Ag/AgCl/KCl(s)) using an accumulation potential of -0.40 V. This peak may be attributed to the reduction of the C=O group. A mean recovery of 99.54%+/-0.23 and a detection limit of 1.65 x 10(-10) M pefloxacin were achieved. After being validated, the proposed procedure was successfully applied for the determination of the drug in tablets and human serum with mean recoveries of 99.57+/-0.48 and 98.55+/-0.78%, respectively. A detection limit of 4.50 x 10(-10) M was achieved for the determination of the drug in human serum. Results of the proposed procedure were comparable with those obtained by reported methods.

  11. Sensitive Adsorptive Voltammetric Method for Determination of Bisphenol A by Gold Nanoparticle/Polyvinylpyrrolidone-Modified Pencil Graphite Electrode.

    Science.gov (United States)

    Yaman, Yesim Tugce; Abaci, Serdar

    2016-05-25

    A novel electrochemical sensor gold nanoparticle (AuNP)/polyvinylpyrrolidone (PVP) modified pencil graphite electrode (PGE) was developed for the ultrasensitive determination of Bisphenol A (BPA). The gold nanoparticles were electrodeposited by constant potential electrolysis and PVP was attached by passive adsorption onto the electrode surface. The electrode surfaces were characterized by electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM). The parameters that affected the experimental conditions were researched and optimized. The AuNP/PVP/PGE sensor provided high sensitivity and selectivity for BPA recognition by using square wave adsorptive stripping voltammetry (SWAdSV). Under optimized conditions, the detection limit was found to be 1.0 nM. This new sensor system offered the advantages of simple fabrication which aided the expeditious replication, low cost, fast response, high sensitivity and low background current for BPA. This new sensor system was successfully tested for the detection of the amount of BPA in bottled drinking water with high reliability.

  12. A Simple, Fast, and Inexpensive Simultaneous Determination of Trace Bismuth(III) and Lead(II) in Water Samples by Adsorptive Stripping Voltammetry

    Science.gov (United States)

    Adamczyk, Marzena

    2017-01-01

    A simple, fast, and inexpensive voltammetric method for the simultaneous determination of trace bismuth(III) and lead(II) using (Hg(Ag)FE) as a working electrode was optimized. For adsorptive stripping voltammetric determination of Bi(III) and Pb(II) in a single scan, the cupferron was applied as a complexing agent. Experimental conditions under which these elements can be simultaneously detected include 0.1 mol L−1 acetate buffer (pH = 4.6), 1 × 10−4 mol L−1 cupferron, accumulation potential −0.05 V, and accumulation time 30 s. The experiments were performed without deaeration of the solutions. The calibration graph was linear from 2 × 10−9 mol L−1 to 1 × 10−7 mol L−1 for the simultaneous presence of bismuth and lead. The detection limits for preconcentration time of 30 s were 6.7 × 10−10 mol L−1 and 8.8 × 10−10 mol L−1 for bismuth and lead, respectively. The application of this procedure was tested by analyzing certified reference material (SPS-WW1 Wastewater) and Lake Zemborzyce water (eastern areas of Poland).

  13. Direct determination of praziquantel in pharmaceutical formulations and human plasma by cathodic adsorptive stripping differential-pulse voltammetry.

    Science.gov (United States)

    Ghoneim, M M; Mabrouk, M M; Tawfik, A

    2002-11-07

    The polarographic and cyclic voltammetric behaviour of praziquantel was studied in B.R. buffers of different pH values. Contradictory to that mentioned in a previously published work, praziquantel is an electro-active compound. Its polarogram exhibited a single 2-electron irreversible reduction wave in B.R. buffer of pH 5, the wave height decreased on the increase of pH till it disappeared in solution of pH >7. This wave was attributed to the reduction of the Cz.dbnd6;O double bond. The quantitative trace determination of bulk praziquantel was studied at a hanging mercury drop electrode by cathodic adsorptive stripping differential-pulse voltammetry. A fully validated sensitive procedure based on controlled adsorptive accumulation of the drug onto a HMDE was developed for its direct determination without derivatization. Accumulation of praziquantel was found to be optimized in 0.1 M Na(2)SO(4) solution as supporting electrolyte under the following conditions: accumulation potential, -1.2 V (vs. Ag/AgCl/KCl(s)); accumulation time, 30 s; scan rate, 10 mV/s and pulse height 100 mV. The proposed procedure was applied successfully for determination of praziquantel in its pharmaceutical formulations and human plasma. The mean recoveries of the drug were 98.85-99.42% and 99.12-100.47% with RSD of 0.49-0.95% and 0.45-0.52% in pharmaceutical formulations and human plasma, respectively. Limits of detection and quantitation of 1.14x10(-9) and 3.80x10(-9) M praziquantel, respectively, were achieved.

  14. Accurate analytical expressions for stripping voltammetry in the Henry adsorption limit.

    Science.gov (United States)

    Calvente, Juan José; Andreu, Rafael

    2011-08-15

    A strategy is developed to derive accurate analytical expressions for low-coverage cathodic stripping voltammetry. The procedure relies on the observation that diffusion affects the location of simulated voltammetric waves but not their shape, provided that physisorption of the analyte is negligible. As a proof of the generality of the proposed approach and having in mind the stripping of thiols, analytical solutions are derived for the cathodic stripping of monomers, dimers, and a mixture of monomers and dimers, whose reliability is proved by their comparison with numerically simulated voltammograms. Application to the deposition and reductive desorption of mercaptoacetic acid at a mercury electrode demonstrates that these approximate solutions can be used to get insights into the interfacial organization of incipient films. For this particular system, a transition from monomeric to dimeric behavior is identified upon increasing the thiol surface concentration. Further generalization of the proposed methodology is achieved by deriving an approximate analytical solution for thin-layer anodic stripping voltammetry, which is satisfactorily compared to the existing summation series solution.

  15. 阿西美辛的吸附伏安特性%Adsorptive Voltammetric Behavior of Acemetacin

    Institute of Scientific and Technical Information of China (English)

    高红艳; 黄鹤; 曾泳淮

    2001-01-01

    In a supporting electrolyte containing HAc-NaAc(pH 4.20) buffer, a reduction peak of acemetacin(ACE) was observed by linear-sweep voltammetry at Hg electrode. The peak showed a potential of -1.18 V(vs. Ag/AgCl) and adsorptive characteristics. The adsorbed species were the neutral molecule of ACE. The saturated adsorption amount of ACE at Hg electrode was 1.19×10-10 mol/cm2, and each ACE molecule occupied 1.43 nm2. On the surface of HMDE, the adsorption of ACE obeyed Frumkin adsorption isotherm. The adsorption coefficient(β) was 1.29×106. The attractive factor(γ) was 1.04. The number of electrons transferred per ACE molecule(n) was 2. The transfer coefficient(α) of the irreversible adsorptive system of ACE was 0.86. The rate constant of surface electrode reaction ks was 0.32 s-1. The mechanism of electrochemical reduction of ACE at Hg electrode was explored. The detection limit of the adsorptive stripping voltammetry of ACE was 1.0×10-9 mol/L under optimized condition.%在乙酸-乙酸钠(pH 4.20)底液中,阿西美辛(ACE)在汞电极上有一线性扫描还原峰,峰电位Epc=-1.18 V(vs. Ag/AgCl),该峰具有明显的吸附性。吸附粒子为ACE中性分子,测得ACE在汞电极上的饱和吸附量为1.19×10-10 mol/cm2,每个ACE分子所占电极面积为1.43 nm2,ACE在悬汞电极上的吸附符合Frumkin等温式。测得吸附系数β=1.29×106,吸引因素γ=1.04,电子转移数n为2,不可逆吸附的电子转移系数α为0.86,表面电极反应速率常数ks=0.32/s。建立了吸附伏安法测定ACE的最佳条件,检出限为1.0×10-9 mol/L。

  16. Square-Wave Voltammetry of Cathodic Stripping Reactions. Diagnostic Criteria, Redox Kinetic Measurements, and Analytical Applications

    OpenAIRE

    Gulaboski, Rubin; Mirceski, Valentin; Komorsky-Lovrić, Šebojka; Lovrić, Milivoj

    2004-01-01

    A comparative study of different types of cathodic stripping reactions under conditions of square-wave voltammetry is presented. Cathodic stripping processes involving reactions of second order as well as reactions coupled by adsorption of the reacting ligand are analyzed The inherent parameters, controlling the overall voltammetric behavior of each cathodic stripping electrode reaction are derived. The criteria for qualitative distinguishing of each mechanism are established as w...

  17. Differential pulse anodic stripping voltammetric determination of lead(II) with a 1,4-bis(prop-2'-enyloxy)-9,10-anthraquinone modified carbon paste electrode.

    Science.gov (United States)

    Mousavi, M F; Rahmani, A; Golabi, S M; Shamsipur, M; Sharghi, H

    2001-08-30

    A sensitive and selective method for the determination of lead(II) with a 1,4-bis(prop-2'-enyloxy)-9,10-anthraquinone (AQ) modified carbon paste electrode has been developed. The method is based on non-electrolytic preconcentration via complex formation with modifier, followed by an accumulation period with a negative potential (-1.5 V), and then by a proper anodic stripping. The analytical performance was evaluated with respect to the quantity of modifier in the paste, concentration of electrolyte solution, preconcentration time, lead(II) concentration, and other variables. A linear calibration graph was obtained in the concentration range 2.00x10(-9)-1.06x10(-5) M Pb(II) (n=21, r=0.9999) with 30 s preconcentration time. The detection limit was found to be 1x10(-9) M. For eight preconcentration/determination cycles, the differential pulse voltammetric response was reproduced with 5.0 and 3.7% relative standard deviations at 2.00x10(-8) and 2.00x10(-6) M Pb(II), respectively. Rapid and convenient renewal of electrode surface allows the use of a single modified electrode surface in multiple analytical determinations over several weeks. Many coexisting metal ions had little or no effect on the determination of lead(II). The developed method was applied to lead determination in waste waters.

  18. Nanogold-penetrated poly(amidoamine) dendrimer for enzyme-free electrochemical immunoassay of cardiac biomarker using cathodic stripping voltammetric method.

    Science.gov (United States)

    Zhang, Bo; Zhang, Yi; Liang, Wenbin; Cui, Bin; Li, Jiabei; Yu, Xuejun; Huang, Lan

    2016-01-21

    Methods based on immunoassays have been developed for cardiac biomarkers, but most involve the low sensitivity and are unsuitable for early disease diagnosis. Herein we design an electrochemical immunoassay for sensitive detection of myoglobin (a cardiac biomarker for acute myocardial infarction) by using nanogold-penetrated poly(amidoamine) dendrimer (AuNP-PAMAM) for signal amplification without the need of natural enzymes. The assay was carried out on the monoclonal mouse anti-myoglobin (capture) antibody-anchored glassy carbon electrode using polyclonal rabbit anti-myoglobin (detection) antibody-labeled AuNP-PAMAM as the signal tag. In the presence of target myoglobin, the sandwiched immunocomplex could be formed between capture antibody and detection antibody. Accompanying AuNP-PAMAM, the carried gold nanoparticles could be directly determined via stripping voltammetric method under acidic conditions. Under optimal conditions, the detectable electrochemical signal increased with the increasing target myoglobin in the sample within a dynamic working range from 0.01 to 500 ng mL(-1) with a detection limit of 3.8 pg mL(-1). The electrochemical immunoassay also exhibited high specificity and good precision toward target myoglobin. Importantly, our strategy could be applied for quantitative monitoring of myoglobin in human serum specimens, giving well matched results with those obtained from commercialized enzyme-linked immunosorbent assay (ELISA) method.

  19. Adsorptive Stripping Voltammetry of Environmental Indicators: Determination of Zinc in Algae

    Science.gov (United States)

    Collado-Sanchez, C.; Hernandez-Brito, J. J.; Perez-Pena, J.; Torres-Padron, M. E.; Gelado-Caballero, M. D.

    2005-01-01

    A method for sample preparation and for the determination of average zinc content in algae using adsorptive stripping voltammetry are described. The students gain important didactic advantages through metal determination in environmental matrices, which include carrying out clean protocols for sampling and handling, and digesting samples using…

  20. Sensitive Adsorptive Voltammetric Method for Determination of Bisphenol A by Gold Nanoparticle/Polyvinylpyrrolidone-Modified Pencil Graphite Electrode

    Directory of Open Access Journals (Sweden)

    Yesim Tugce Yaman

    2016-05-01

    Full Text Available A novel electrochemical sensor gold nanoparticle (AuNP/polyvinylpyrrolidone (PVP modified pencil graphite electrode (PGE was developed for the ultrasensitive determination of Bisphenol A (BPA. The gold nanoparticles were electrodeposited by constant potential electrolysis and PVP was attached by passive adsorption onto the electrode surface. The electrode surfaces were characterized by electrochemical impedance spectroscopy (EIS and scanning electron microscopy (SEM. The parameters that affected the experimental conditions were researched and optimized. The AuNP/PVP/PGE sensor provided high sensitivity and selectivity for BPA recognition by using square wave adsorptive stripping voltammetry (SWAdSV. Under optimized conditions, the detection limit was found to be 1.0 nM. This new sensor system offered the advantages of simple fabrication which aided the expeditious replication, low cost, fast response, high sensitivity and low background current for BPA. This new sensor system was successfully tested for the detection of the amount of BPA in bottled drinking water with high reliability.

  1. The versatility of salicylaldehyde thiosemicarbazone in the determination of copper in blood using adsorptive stripping voltammetry.

    Science.gov (United States)

    Mahajan, Rakesh Kumar; Walia, T P S; Sumanjit; Lobana, T S

    2005-10-15

    The adsorptive cathodic stripping voltammetry technique (AdCSV) is used to determine copper(II) using salicylaldehyde thiosemicarbazone (N, S- donor) as a complexing agent on hanging mercury drop electrode at pH 9.3. Variable factors affecting the response, i.e. the concentration of ligand, pH, adsorption potential and adsorption time are assessed and optimized. The adsorbed complex of copper(II) and salicylaldehyde thiosemicarbazone gives a well defined cathodic stripping peak current at -0.35 V, which has been used for the determination of copper in the concentration range of 7.85 x 10(-9) to 8.00 x 10(-6)M with accumulation time of 360 s at -0.1 V versus Ag/AgCl. This technique has been applied for the determination of copper in various digested samples of whole blood at trace levels.

  2. Complexation-Based Detection of Nickel(II at a Graphene-Chelate Probe in the Presence of Cobalt and Zinc by Adsorptive Stripping Voltammetry

    Directory of Open Access Journals (Sweden)

    Keagan Pokpas

    2017-07-01

    Full Text Available The adsorptive stripping voltammetric detection of nickel and cobalt in water samples at metal film electrodes has been extensively studied. In this work, a novel, environmentally friendly, metal-free electrochemical probe was constructed for the ultra-trace determination of Ni2+ in water samples by Adsorptive Cathodic Stripping Voltammetry (AdCSV. The electrochemical platform is based on the adsorptive accumulation of Ni2+ ions directly onto a glassy carbon electrode (GCE modified with dimethylglyoxime (DMG as chelating agent and a Nafion-graphene (NGr nanocomposite to enhance electrode sensitivity. The nafion-graphene dimethylglyoxime modified glassy carbon electrode (NGr-DMG-GCE shows superior detection capabilities as a result of the improved surface-area-to-volume ratio and enhanced electron transfer kinetics following the incorporation of single layer graphene, while limiting the toxic effects of the sensor by removal of the more common mercury, bismuth and lead films. Furthermore, for the first time the NGr-DMG-GCE, in the presence of common interfering metal ions of Co2+ and Zn2+ demonstrates good selectivity and preferential binding towards the detection of Ni2+ in water samples. Structural and morphological characterisation of the synthesised single layer graphene sheets was conducted by Raman spectrometry, HRTEM and HRSEM analysis. The instrumental parameters associated with the electrochemical response, including accumulation potential and accumulation time were investigated and optimised in addition to the influence of DMG and graphene concentrations. The NGr-DMG-GCE demonstrated well resolved, reproducible peaks, with RSD (% below 5% and a detection limit of 1.5 µg L−1 for Ni2+ reduction at an accumulation time of 120 s., the prepared electrochemical sensor exhibited good detection and quantitation towards Ni2+ detection in tap water samples, well below 0.1 mg L−1 set by the WHO and EPA standards. This comparable to the South

  3. Complexation-Based Detection of Nickel(II) at a Graphene-Chelate Probe in the Presence of Cobalt and Zinc by Adsorptive Stripping Voltammetry.

    Science.gov (United States)

    Pokpas, Keagan; Jahed, Nazeem; Baker, Priscilla G; Iwuoha, Emmanuel I

    2017-07-25

    The adsorptive stripping voltammetric detection of nickel and cobalt in water samples at metal film electrodes has been extensively studied. In this work, a novel, environmentally friendly, metal-free electrochemical probe was constructed for the ultra-trace determination of Ni(2+) in water samples by Adsorptive Cathodic Stripping Voltammetry (AdCSV). The electrochemical platform is based on the adsorptive accumulation of Ni(2+) ions directly onto a glassy carbon electrode (GCE) modified with dimethylglyoxime (DMG) as chelating agent and a Nafion-graphene (NGr) nanocomposite to enhance electrode sensitivity. The nafion-graphene dimethylglyoxime modified glassy carbon electrode (NGr-DMG-GCE) shows superior detection capabilities as a result of the improved surface-area-to-volume ratio and enhanced electron transfer kinetics following the incorporation of single layer graphene, while limiting the toxic effects of the sensor by removal of the more common mercury, bismuth and lead films. Furthermore, for the first time the NGr-DMG-GCE, in the presence of common interfering metal ions of Co(2+) and Zn(2+) demonstrates good selectivity and preferential binding towards the detection of Ni(2+) in water samples. Structural and morphological characterisation of the synthesised single layer graphene sheets was conducted by Raman spectrometry, HRTEM and HRSEM analysis. The instrumental parameters associated with the electrochemical response, including accumulation potential and accumulation time were investigated and optimised in addition to the influence of DMG and graphene concentrations. The NGr-DMG-GCE demonstrated well resolved, reproducible peaks, with RSD (%) below 5% and a detection limit of 1.5 µg L(-1) for Ni(2+) reduction at an accumulation time of 120 s., the prepared electrochemical sensor exhibited good detection and quantitation towards Ni(2+) detection in tap water samples, well below 0.1 mg L(-1) set by the WHO and EPA standards. This comparable to the South

  4. Determination of Total Germanium in Chinese Herbal Remedies by Square-Wave Catalytic Adsorptive Cathodic Stripping Voltammetry at an Improved Bismuth Film Electrode

    Directory of Open Access Journals (Sweden)

    Shangwei Zhong

    2013-01-01

    Full Text Available A catalytic adsorptive cathodic stripping voltammetric method on an improved bismuth film electrode (BiFE for the determination of trace germanium in the presence of pyrogallol has been investigated. A well-defined and sensitive stripping peak of Ge(IV-pyrogallol complex was observed at −0.79 V (versus SCE in a 0.1 M acetate buffer solution (pH 4.8 at a deposition potential of −0.34 V. The reduction current is catalytically enhanced by adding KBrO3. The experimental variables and potential interference were studied. Compared with the BiFE plated in the solution prepared based on HAc-NaAc without trisodium citrate, the improved BiFE electrodeposited in the solution of HAc-NaAc containing trisodium citrate displayed a better electroanalytical performance for the determination of germanium(IV. Under the optimized conditions, the detection limit of Ge(IV was 60 ng L−1, and the relative standard deviation (RSD was 3.73% at 5 μg L−1 level (n=9. This method was successfully applied to determine the total germanium in several Chinese herbal remedies.

  5. Cathodic stripping voltammetric determination of chromium in coastal waters on cubic Nano-titanium carbide loaded gold nanoparticles modified electrode

    Directory of Open Access Journals (Sweden)

    Haitao eHan

    2015-09-01

    Full Text Available The novel cubical nano-titanium carbide loaded gold nanoparticles modified electrode for selective and sensitive detection of trace chromium (Cr in coastal water was established based on a simple approach. Nano-titanium carbide is used as the typical cubical nanomaterial with wonderful catalytic activity towards the reduction of Cr(VI. Gold nanoparticles with excellent physical and chemical properties can facilitate electron transfer and enhance the catalytic activity of the modified electrode. Taking advantage of the synergistic effects of nano-titanium carbide and gold nanoparticles, the excellent cathodic signal responses for the stripping determination of Cr(VI can be obtained. The detection limit of this method is calculated as 2.08 μg L-1 with the linear calibration curve ranged from 5.2 to 1040 μg L-1. This analytical method can be used to detect Cr(VI effectively without using any complexing agent. The fabricated electrode was successfully applied for the detection of chromium in coastal waters collected from the estuary giving Cr concentrations between 12.48 and 22.88 μg L-1 with the recovery between 96% and 105%.

  6. LabVIEW-based sequential-injection analysis system for the determination of trace metals by square-wave anodic and adsorptive stripping voltammetry on mercury-film electrodes.

    Science.gov (United States)

    Economou, Anastasios; Voulgaropoulos, Anastasios

    2003-01-01

    The development of a dedicated automated sequential-injection analysis apparatus for anodic stripping voltammetry (ASV) and adsorptive stripping voltammetry (AdSV) is reported. The instrument comprised a peristaltic pump, a multiposition selector valve and a home-made potentiostat and used a mercury-film electrode as the working electrodes in a thin-layer electrochemical detector. Programming of the experimental sequence was performed in LabVIEW 5.1. The sequence of operations included formation of the mercury film, electrolytic or adsorptive accumulation of the analyte on the electrode surface, recording of the voltammetric current-potential response, and cleaning of the electrode. The stripping step was carried out by applying a square-wave (SW) potential-time excitation signal to the working electrode. The instrument allowed unattended operation since multiple-step sequences could be readily implemented through the purpose-built software. The utility of the analyser was tested for the determination of copper(II), cadmium(II), lead(II) and zinc(II) by SWASV and of nickel(II), cobalt(II) and uranium(VI) by SWAdSV.

  7. Adsorption and desorption of bis-(3-sulfopropyl) disulfide during Cu electrodeposition and stripping at Au electrodes.

    Science.gov (United States)

    Chiu, Yong-Da; Dow, Wei-Ping; Krug, Klaus; Liu, Yung-Fang; Lee, Yuh-Lang; Yau, Shueh-Lin

    2012-10-09

    The adsorption and desorption of bis-(3-sulfopropyl) disulfide (SPS) on Cu and Au electrodes and its electrochemical effect on Cu deposition and dissolution were examined using cyclic voltammetry stripping (CVS), field-emission scanning electron microscopy (FESEM), and X-ray photoelectron spectroscopy (XPS). SPS dissociates into 3-mercapto-1-propanesulfonate when it is contacted with Au and Cu electrodes, producing Cu(I)- and Au(I)-thiolate species. These thiolates couple with chloride ions and promote not only the reduction of Cu(2+) in Cu deposition but also the oxidation of Cu(0) to Cu(+) in Cu stripping. During Cu electrodeposition on the SPS-modified Au electrode, thiolates transfer from Au onto the Cu underpotential deposition (UPD) layer. The Cu UPD layer stabilizes a large part of the transferred thiolates which subsequently is buried by the Cu overpotential deposition (OPD) layer. The buried thiolates reappear on the Au electrode after the copper deposit is electrochemically stripped off. A much smaller part of thiolates transfers to the top of the Cu OPD layer. In contrast, when SPS preadsorbs on a Cu-coated Au electrode, almost all of the adsorbed SPS leaves the Cu surface during Cu electrochemical stripping and does not return to the uncovered Au surface. A reaction mechanism is proposed to explain these results.

  8. Voltammetric Determination of Ni and Co in Water Samples

    Science.gov (United States)

    Herrera-Melian, Jose Alberto; Dona-Rodriguez, Jose Miguel; Hernandez-Brito, Joaquin; Perez Pena, Jesus

    1997-12-01

    Stripping voltammetry has attracted considerable attention for the determination of trace and ultratrace metals. This is mainly due to its high sensitivity and low cost of instrumentation. In adsorptive stripping voltammetry an organometallic complex is formed by the addition of a suitable ligand to the sample. The complex is adsorbed onto the Hg-drop by the application of the proper adsorption potential (more positive than E1/2) and solution stirring. After an adsorption period a cathodic (negative going) potential scan is applied and the metal concentration is calculated by the standard addition method. Nickel is found in natural waters at nM levels and is closely related with phosphates and silicates. Cobalt is a component of vitamin B12 and occurs in natural waters at concentration about 0.1 nM. We propose the voltammetric analysis of these elements by adsorptive stripping voltammetry as an introductory laboratory experiment for advanced chemistry or for chemical or environmental engineering students. The experiment has been proven to be very suitable for the laboratory part of the instrumental analysis course at the University of Las Palmas de Gran Canaria (Spain). In general, about 70% of the students have obtained good agreement (less than 10% of difference) between their results and the expected ones. Two hours is enough for the overall instrumental performance and the preparation of Ni and Co standards.

  9. Trace vanadium analysis by catalytic adsorptive stripping voltammetry using mercury-coated micro-wire and polystyrene-coated bismuth film electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Dansby-Sparks, Royce; Chambers, James Q. [Department of Chemistry, University of Tennessee, Knoxville, TN 37996-1600 (United States); Xue Ziling, E-mail: xue@ion.chem.utk.edu [Department of Chemistry, University of Tennessee, Knoxville, TN 37996-1600 (United States)

    2009-06-08

    An electrochemical technique has been developed for ultra-trace (ng L{sup -1}) vanadium (V) measurement. Catalytic adsorptive stripping voltammetry for V analysis was developed at mercury-coated gold micro-wire electrodes (MWEs, 100 {mu}m) in the presence of gallic acid (GA) and bromate ion. A potential of -0.275 V (vs Ag/AgCl) was used to accumulate the complex in acetate buffer (pH 5.0) at the electrode surface followed by a differential pulse voltammetric scan. Parameters affecting the electrochemical response, including pH, concentration of GA and bromate, deposition potential and time have been optimized. Linear response was obtained in the 0-1000 ng L{sup -1} range (2 min deposition), with a detection limit of 0.88 ng L{sup -1}. The method was validated by comparison of results for an unknown solution of V by atomic absorption measurement. The protocol was evaluated in a real sample by measuring the amount of V in river water samples. Thick bismuth film electrodes with protective polystyrene films have also been made and evaluated as a mercury free alternative. However, ng L{sup -1} level detection was only attainable with extended (10 min) deposition times. The proposed use of MWEs for the detection of V is sensitive enough for future use to test V concentration in biological fluids treated by the advanced oxidation process (AOP).

  10. Trace vanadium analysis by catalytic adsorptive stripping voltammetry using mercury-coated micro-wire and polystyrene-coated bismuth film electrodes.

    Science.gov (United States)

    Dansby-Sparks, Royce; Chambers, James Q; Xue, Zi-Ling

    2009-06-08

    An electrochemical technique has been developed for ultra-trace (ng L(-1)) vanadium (V) measurement. Catalytic adsorptive stripping voltammetry for V analysis was developed at mercury-coated gold micro-wire electrodes (MWEs, 100 microm) in the presence of gallic acid (GA) and bromate ion. A potential of -0.275 V (vs Ag/AgCl) was used to accumulate the complex in acetate buffer (pH 5.0) at the electrode surface followed by a differential pulse voltammetric scan. Parameters affecting the electrochemical response, including pH, concentration of GA and bromate, deposition potential and time have been optimized. Linear response was obtained in the 0-1000 ng L(-1) range (2 min deposition), with a detection limit of 0.88 ng L(-1). The method was validated by comparison of results for an unknown solution of V by atomic absorption measurement. The protocol was evaluated in a real sample by measuring the amount of V in river water samples. Thick bismuth film electrodes with protective polystyrene films have also been made and evaluated as a mercury free alternative. However, ng L(-1) level detection was only attainable with extended (10 min) deposition times. The proposed use of MWEs for the detection of V is sensitive enough for future use to test V concentration in biological fluids treated by the advanced oxidation process (AOP).

  11. Assay of dipyridamole in human serum using cathodic adsorptive square-wave stripping voltammetry.

    Science.gov (United States)

    Ghoneim, M M; Tawfik, A; Radi, A

    2002-09-01

    A rapid and sensitive square-wave voltammetric procedure was optimized for the determination of dipyridamole after its adsorption preconcentration onto a hanging mercury drop electrode. The peak current of the first of the two peaks developed for this drug in Britton-Robinson buffer at pH 8.0 has been considered for the present analytical study. An accumulation potential of -1.0 V versus Ag/AgCl/KCl(s), pulse amplitude a =100 mV, scan increment Delta E =10 mV, and frequency f =120 Hz were the optimal experimental parameters. Dipyridamole can be determined in the concentration range of 9.0 x 10(-9) to 5.0 x 10(-6) M using accumulation times of 30-300 s. A detection limit of 4.0 x 10(-11) M was achieved after a 300 s accumulation time. Applicability to serum samples was illustrated. The average recoveries for dipyridamole spiked to serum at 0.25-4.50 micro g ml(-1) were 96.0-102.0%, and the higher standard deviation was 2.9%. A detection limit of 0.06 micro g mL(-1) of serum was obtained.

  12. Determination of copper in whole blood by differential pulse adsorptive stripping voltammetry

    Directory of Open Access Journals (Sweden)

    Tarik Attar

    2014-02-01

    Full Text Available A selective and sensitive method for determination of copper in blood by adsorptive differential pulse cathodic stripping voltammetry is presented. The method is based on adsorptive accumulation of the complexes of Cu (II ions with benzenesulfonyl hydrazide onto hanging mercury drop electrode (HMDE, followed by the reduction of the adsorbed species by differential pulse cathodic stripping voltammetry. The effect of various parameters such as supporting electrolyte, concentration of benzenesulfonyl hydrazide, accumulation potential, accumulation time and stirring rate on the selectivity and sensitivity were studied. The optimum conditions for determination of copper include perchloric acid 0.03 M, concentration of benzenesulfonyl hydrazide 7.5×10-5 M, the accumulation potential of -350 mV (vs. Ag/AgCl, the accumulation time of 50 s, and the scan rate of 50 mV s-1. Under optimized conditions, linear calibration curves were established for the concentration of Cu (II in the range of 0.62-275 ng mL-1, with detection limit of 0.186 ng mL-1 for Cu (II. The procedure was successfully applied to the determination of copper ion in whole blood samples.

  13. Adsorptive stripping voltammetry of antibiotics rifamycin SV and rifampicin at renewable pencil electrodes.

    Science.gov (United States)

    Kawde, Abdel-Nasser; Temerk, Yassein; Farhan, Nasser

    2014-01-01

    Adsorptive stripping voltammetry of antibiotics of rifamycin SV (RSV) and rifampicin (RIF) was investigated by cyclic voltammetry and differential pulse voltammetry using a renewable pencil graphite electrode (PGE). The nature of the oxidation process of RSV and RIF taking place at the PGE was characterized. The results show that the determination of highly sensitive oxidation peak current is the basis of a simple, accurate and rapid method for quantification of RSV and RIF in bulk forms, pharmaceutical formulations and biological fluids by differential pulse adsorptive stripping voltammetry (DPASV). Factors influencing the trace measurement of RSV and RIF at PGE are assessed. The limits of detection for the determination of RSV and RIF in bulk forms are 6.0 × 10(-8) mol/L and 1.3 × 10(-8) mol/L, respectively. Moreover, the proposed procedure was successfully applied to assay both RSV and RIF in pharmaceutical formulations and in biological fluids. The capability of the proposed procedure for simultaneous assay of antibiotics RSV-isoniazid and RIF-isoniazid was achieved. The statistical analysis and calibration curve data for trace determination of RSV and RIF are reported.

  14. Direct determination of molybdenum in seawater by adsorption cathodic stripping square-wave voltammetry.

    Science.gov (United States)

    Sun, Y C; Mierzwa, J; Lan, C R

    2000-06-30

    A reliable and very sensitive procedure for the determination of trace levels of molybdenum in seawater is proposed. The complex of molybdenum with 8-hydroxyquinoline (Oxine) is analyzed by cathodic stripping square-wave voltammetry based on the adsorption collection onto a hanging mercury drop electrode (HMDE). This procedure of molybdenum determination was found to be more favorable than differential pulse cathodic stripping voltammetry because of inherently faster scan rate and much better linearity obtained through the one-peak (instead of one-of-two peaks) calibration. The variation of polarographic peak and peak current with a pH, adsorption time, adsorption potential, and some instrumental parameters such as scan rate and pulse height were optimized. The alteration of polarographic wave and its likely mechanism are also discussed. The relationship between peak current and molybdenum concentration is linear up to 150 mug l(-1). Under the optimal analytical conditions, the determination limit of 0.5 mug l(-1) Mo was reached after 60 s of the stirred collection. The estimated detection limit is better than 0.1 mug l(-1) of Mo. The applicability of this method to analysis of seawater was assessed by the determination of molybdenum in two certified reference seawater samples (CASS-2 and NASS-2) and the comparison of the analytical results for real seawater samples (study on a vertical distribution of Mo in the seawater column) with the results obtained by Zeeman-corrected electrothermal atomization atomic absorption spectrometry (Zeeman ETAAS). A good agreement between two used methods of molybdenum determination was obtained.

  15. Determination of losartan and triamterene in pharmaceutical compounds and urine using cathodic adsorptive stripping voltammetry.

    Science.gov (United States)

    Ensafi, Ali Asghar; Hajian, Reza

    2008-01-01

    A square-wave voltammetric procedure for the electroanalytical determination of losartan and triamterene in Britton-Robinson buffer (pH 3.0, 0.1 mol L(-1)) as a supporting electrolyte containing 30 ng mL(-1) of copper ions was developed. Opposite to the case of triamterene, losartan can not be reduced at a mercury electrode alone, but a new peak appears at -0.25 V in the presence of copper due to the formation of a complex between copper(II) and losartan. An accumulation potential of -0.30 V during 80 s for the prior adsorption of losartan-copper(II) and triamterene on the electrode surface was used. The response of the system was found to be linear in the range of 30.0 - 270.0 nmol L(-1) for losartan and two linear dynamic ranges containing 0.5-200.0 and 200.0-400.0 nmol L(-1) of triamterene. The limits of detections were 9.7 and 0.3 nmol L(-1) for losartan and triamterene, respectively. The relative standard deviations for five replicate analyses of 100.0 and 10.0 nmol L(-1) losartan and triamterene were 5.5%. Applicability to assay the drugs in urine and pharmaceutical formulations was illustrated with satisfactory results. The direct-current polarography of triamterene indicates that the reduction of a related drug is strongly dependent on the pH of the solution. A linear segment was found with slope value of -63.6 mV pH(-1) in the pH range of 2.0 - 6.0. The stoichiometry and complex formation constant (beta) for losartan-Cu(II), number of transfer electrons (n), transfer coefficients (alpha) and number of proton transfers were also estimated.

  16. Electrochemistry and analytical determination of lysergic acid diethylamide (LSD) via adsorptive stripping voltammetry.

    Science.gov (United States)

    Merli, Daniele; Zamboni, Daniele; Protti, Stefano; Pesavento, Maria; Profumo, Antonella

    2014-12-01

    Lysergic acid diethylamide (LSD) is hardly detectable and quantifiable in biological samples because of its low active dose. Although several analytical tests are available, routine analysis of this drug is rarely performed. In this article, we report a simple and accurate method for the determination of LSD, based on adsorptive stripping voltammetry in DMF/tetrabutylammonium perchlorate, with a linear range of 1-90 ng L(-1) for deposition times of 50s. LOD of 1.4 ng L(-1) and LOQ of 4.3 ng L(-1) were found. The method can be also applied to biological samples after a simple extraction with 1-chlorobutane. Copyright © 2014 Elsevier B.V. All rights reserved.

  17. Determination of Lamotrigine in Pharmaceutical Preparations by Adsorptive Stripping Voltammetry Using Screen Printed Electrodes

    Science.gov (United States)

    Domínguez-Renedo, Olga; Calvo, M. Encarnación Burgoa; Arcos-Martínez, M. Julia

    2008-01-01

    This paper describes a procedure that has been optimized for the determination of lamotrigine by Differential Pulse Adsorptive Stripping Voltammetry (DPAdSV) using carbon screen-printed electrodes (CSPE) and mercury coated carbon screen-printed electrodes. Selection of the experimental parameters was made using experimental design methodology. The detection limit found was 5.0 × 10-6 M and 2.0 × 10-6 M for the non modified and Hg modified CSPE, respectively. In terms of reproducibility, the precision of the above mentioned methods was calculated in %RSD values at 9.83% for CSPE and 2.73% for Hg-CSPE. The Hg-coated CSPEs developed in this work were successfully applied in the determination of lamotrigine in pharmaceutical preparations. PMID:27879931

  18. Determination of selenium in natural waters by adsorptive differential pulse cathodic stripping voltammetry.

    Science.gov (United States)

    Ashournia, Mehdi; Aliakbar, Alireza

    2009-08-30

    In this work bovine albumin was used innovatively as a medium for adsorptive accumulation of Se-I(2) on thin mercury film electrode. Se-I(2) was formed by reaction between Se(IV) and iodide in HCl media. The adsorbed Se-I(2) was stripped in 0.05 M HCl by differential pulse cathodic potential scan. The proposed method was successfully applied to analysis of Se(IV) and Se(VI) in natural waters sampled from some lagoons south of Caspian Sea. The optimum reaction conditions and other analytical parameters and influence of cations and anions were studied. The detection limit was 0.37 ng mL(-1). The obtained results were compared with the results of DPCSV after electrochemical preconcentration, HG-AAS and ICP-AES.

  19. Determination of Lamotrigine in Pharmaceutical Preparations by Adsorptive Stripping Voltammetry Using Screen Printed Electrodes

    Directory of Open Access Journals (Sweden)

    M. Julia Arcos-Martínez

    2008-07-01

    Full Text Available This paper describes a procedure that has been optimized for the determination of lamotrigine by Differential Pulse Adsorptive Stripping Voltammetry (DPAdSV using carbon screen-printed electrodes (CSPE and mercury coated carbon screen-printed electrodes. Selection of the experimental parameters was made using experimental design methodology. The detection limit found was 5.0 x 10-6 M and 2.0 x 10-6 M for the non modified and Hg modified CSPE, respectively. In terms of reproducibility, the precision of the above mentioned methods was calculated in %RSD values at 9.83% for CSPE and 2.73% for Hg-CSPE. The Hg-coated CSPEs developed in this work were successfully applied in the determination of lamotrigine in pharmaceutical preparations.

  20. Catalytic Adsorptive Stripping Voltammetry at a Carbon Paste Electrode for the Determination of Amiodarone

    Institute of Scientific and Technical Information of China (English)

    LIU Ning; GAO Wei; SONG Jun-Feng

    2006-01-01

    Voltammetry using solid electrodes usually suffers from the contamination due to the deposition of the redox products of analytes on the electrode surface. The contamination has resulted in poor reproducibility and overelaborate operation procedures. The use of the chemical catalysis of oxidant on the reduction product of analyte not only can eliminate the contamination of analyte to solid electrodes but also can improve the faradaic response of analyte. This work introduced both the catalysis of oxidant K2S2O8 and the enhancement of surfactant Triton X-100 on the faraday response of amiodarone into an adsorptive stripping voltammetry at a carbon paste electrode for the determination of amiodarone. The method exhibits high sensitivity, good reproducibility and simple operation procedure. In 0.2 mol·L-1 HOAc-NaOAc buffer (pH=5.3) containing 2.2 × 10-2 mol·L-1 K2S2O8 and 0.002% Triton X-100, the 2.5th-order derivative stripping peak current of the catalytic wave at 0.3 V (vs. Ag/AgCl) is rectilinear to amiodarone concentration in the range of 2.0× 10-10-2.3× 10-8 mol·L-1 with a detection limit of 1.5× l0-10 mol·L-1 after accumulation at 0 V for 30 s.

  1. Cathodic adsorptive stripping voltammetry of an anti-emetic agent Granisetron in pharmaceutical formulation and biological matrix

    Institute of Scientific and Technical Information of China (English)

    Rajeev Jain; Ramkishor Sharma

    2012-01-01

    Granisetron showed one well-defined reduction peak at Hanging Mercury Drop Electrode (HMDE) in the potential range from -1.3 to -1.5 V due to reduction of C=N bond. Solid-phase extraction technique was employed for extraction of Granisetron from spiked human plasma. Granisetron showed peak current enhancement of 4.45% at square-wave voltammetry and 5.33% at cyclic voltammetry as compared with the non stripping techniques. The proposed voltammetric method allowed quantification of Granisetron in pharmaceutical formulation over the target concentration range of 5-200 ng/mL with detection limit 13.63 ng/mL, whereas in human plasma 50-225 ng/mL with detection limit 11.75 ng/mL.

  2. Determination of trace amounts of morphine in human plasma by anodic adsorptive stripping differential pulse voltammetry

    Institute of Scientific and Technical Information of China (English)

    Ali Niazi; Ateesa Yazdanipour

    2008-01-01

    New adsorptive anodic differential pulse stripping voltammetry method for the direct determination of morphine at trace levels in human plasma of addicts is proposed.The procedure involves an adsorptive accumulation of morphine on a HMDE,followed by oxidation of adsorbed morphine by voltammetry scan using differential pulse modulation.The optimum conditions for the analysis of morphine are pH 10.5,Eacc of - 100 mV (vs.Ag/AgCl),and tacc of 120 s.The peak current is proportional to the concentration of morphine,and a linear calibration graph is obtained at 0.01-3.10 μg mL-1.A relative standard deviation of 1.06% (n=5) was obtained,and the limit of detection was 3 ng mL- 1.The capability of the method for the analysis of real samples was evaluated by the determination of morphine in spiked human plasma and addicts human plasma with satisfactory results.

  3. Determination of trace cobalt concentrations in human serum by adsorptive stripping voltammetry.

    Science.gov (United States)

    Kajic, Petra; Milosev, Ingrid; Pihlar, Boris; Pisot, Venceslav

    2003-01-01

    The goal of our study was to develop an accurate and reliable method for determining trace cobalt concentrations in human serum. The method was used to determine cobalt in the sera of healthy persons and patients with orthopaedic implants containing cobalt - a possible source of systemic release of cobalt into the human body. This goal is of vital interest since cobalt and its compounds are classified by IARC as potentially carcinogenic to humans. We used an electrochemical method, adsorptive stripping voltammetry (AdSV), which made possible the low detection limit and high sensitivity needed for measurements in human serum. The serum was acid digested by a combination of H2SO4, HNO3 and H2O2 in a 10 mL Kjeldhal flask. The digested sample was then dissolved in 0.1 mol/L ammonia buffer, pH 9.0 +/- 0.2. The determination is based on the adsorptive collection of the complex of cobalt (II) with dimethylglyoxime on a hanging mercury drop electrode (HMDE). The optimum values of adsorption potential and time were determined to be -0.8 V and 60 s. The optimisation of the sample digestion protocol and measurement procedures ensured the reliable assessment of low cobalt concentrations, down to 0.03 microg/L. The mean concentration of serum cobalt in four healthy persons was 0.11 +/- 0.06 microg/L, and in four patients with total hip replacements 0.34 +/- 0.07 microg/L. This method will be used routinely for measuring serum cobalt levels in patients with total hip replacements.

  4. Electrochemistry of moexipril: experimental and computational approach and voltammetric determination.

    Science.gov (United States)

    Taşdemir, Hüdai I; Kiliç, E

    2014-09-01

    The electrochemistry of moexipril (MOE) was studied by electrochemical methods with theoretical calculations performed at B3LYP/6-31 + G (d)//AM1. Cyclic voltammetric studies were carried out based on a reversible and adsorption-controlled reduction peak at -1.35 V on a hanging mercury drop electrode (HMDE). Concurrently irreversible diffusion-controlled oxidation peak at 1.15 V on glassy carbon electrode (GCE) was also employed. Potential values are according to Ag/AgCI, (3.0 M KCI) and measurements were performed in Britton-Robinson buffer of pH 5.5. Tentative electrode mechanisms were proposed according to experimental results and ab-initio calculations. Square-wave adsorptive stripping voltammetric methods have been developed and validated for quantification of MOE in pharmaceutical preparations. Linear working range was established as 0.03-1.35 microM for HMDE and 0.2-20.0 microM for GCE. Limit of quantification (LOQ) was calculated to be 0.032 and 0.47 microM for HMDE and GCE, respectively. Methods were successfully applied to assay the drug in tablets by calibration and standard addition methods with good recoveries between 97.1% and 106.2% having relative standard deviation less than 10%.

  5. Is microwave digestion using TFM vessels a suitable preparation method for Pt determination in biological samples by adsorptive cathodic stripping voltammetry?

    Science.gov (United States)

    Haus, Nadine; Eybe, Tanja; Zimmermann, Sonja; Sures, Bernd

    2009-03-02

    The occurrence of Pt in environmental matrices is increasing since the introduction of automobile catalytic converters. Given that Pt is bioavailable and causes biological effects in plants and animals, respective biomonitoring programs are in high demand. But the analytical methods for conducting such programs have not yet been sufficiently established. Therefore, a study was carried out to develop a microwave digestion of biological samples, which allows a rapid determination of Pt by adsorptive cathodic stripping voltammetry. A high pressure microwave system was used and the digestion was performed in HNO(3) and HCl. After digestion the HNO(3) was evaporated with a microwave assisted vacuum concentration set. The study resulted in a procedural detection limit of 37.5 ng L(-1) and a relative standard deviation of 18%. A recovery study resulted in a Pt loss below 5%. The microwave assisted evaporation of HNO(3) performed satisfactorily and up to 500 mL of the sample solution could be used for the voltammetric measurements without any effect on the peak heights. A direct comparison of Pt concentrations conducted after microwave digestion and digestion by high pressure ashing showed similar values. However, these promising results were not persistent throughout the repeated analysis using the same Teflon vessels. The vessels did not endure the harsh conditions and due to aging processes the Pt loss consistently increased until Pt determination in environmental relevant concentrations became impossible. Quartz vessels could not be employed as an alternative to the Teflon vessels, due to a lack of compatibility with the vacuum concentration system. Consequently, the results of this paper show that there is a need for further development of more resistant Teflon materials.

  6. ADSORPTIVE VOLTAMMETRIC BEHAVIOR OF OMEPRAZOLE AND ITS APPLICATION%奥美拉唑的吸附伏安特性及其应用

    Institute of Scientific and Technical Information of China (English)

    曹尔新; 曾泳淮

    2001-01-01

    目的研究奥美拉唑(omeprazole,OPZ)的电化学行为,拟定测定OPZ的吸附溶出伏安法。方法用单扫示波极谱法、循环伏安法等技术进行研究。结果在0.1 mol*L-1 NH3-NH4Cl (pH 8.90)底液中,OPZ在汞电极上有一线性扫描还原峰,其峰电位Ep=-1.04 V (vs Ag/AgCl),该峰有明显的吸附性。吸附粒子为OPZ中性分子,测得OPZ在汞电极上的饱和吸附量Γs=9.55×10-11 mol*cm-2,每个OPZ分子所占电极面积为1.74 nm2,OPZ在汞电极上的吸附符合Frumkin吸附等温式。测得吸附系数β=1.32×106,25℃时的吸附自由能ΔGθ=-34.93 kJ*mol-1,电极反应电子数n=4,不可逆体系动力学参数αnα=0.78,表面电极反应速率常数ks=0.18 s-1,OPZ在溶液中的扩散系数D=1.03×10-5 cm2*s-1。建立了吸附溶出伏安法测定OPZ的最佳条件,检出限为2.0×10-9 mol*L-1。结论证实该体系为具有吸附性的不可逆过程。%AIM To study the electrochemical behavior of omeprazole (OPZ) and a new method for the determination of the compound was established by adsorptive stripping voltammetry. METHODS Linear-sweep polarography and cyclic voltammetry were used. RESULTS In a supporting electrolyte containing 0.1 mol*L-1 NH3-NH4Cl, a reduction peak of OPZ was observed by linear-sweep voltammetry at Hg electrode. The peak showed a potential of -1.04 V (vs Ag/AgCl at 100 mV*s-1) and adsorptive characteristics. The adsorbed species is most probably the neutral molecular of OPZ. The saturated adsorption of OPZ at Hg electrode is 9.55×10-11 mol*cm-2 and every OPZ molecule occupies an area of 1.74 nm2. On the surface of the hanging mercury drop electrode, the adsorption of OPZ obeys Frumkin adsorption isotherm. The adsorption coefficient β is 1.32×106, the Gibbs energy of adsorption ΔGθ is -34.93 kJ*mol-1, the number of electrons transferred n is 4, the kinetics parameter αnα is 0.78, the rate constant of the surface electrode reaction ks is 0.18 s-1, the diffusion coefficient

  7. Determination of oleuropein using multiwalled carbon nanotube modified glassy carbon electrode by adsorptive stripping square wave voltammetry.

    Science.gov (United States)

    Cittan, Mustafa; Koçak, Süleyman; Çelik, Ali; Dost, Kenan

    2016-10-01

    A multi-walled carbon nanotube modified glassy carbon electrode was used to prepare an electrochemical sensing platform for the determination of oleuropein. Results showed that, the accumulation of oleuropein on the prepared electrode takes place with the adsorption process. Electrochemical behavior of oleuropein was studied by using cyclic voltammetry. Compared to the bare GCE, the oxidation peak current of oleuropein increased about 340 times at MWCNT/GCE. Voltammetric determination of oleuropein on the surface of prepared electrode was studied using square wave voltammetry where the oxidation peak current of oleuropein was measured as an analytical signal. A calibration curve of oleuropein was performed between 0.01 and 0.70µM and a good linearity was obtained with a correlation coefficient of 0.9984. Detection and quantification limits of the method were obtained as 2.73 and 9.09nM, respectively. In addition, intra-day and inter-day precision studies indicated that the voltammetric method was sufficiently repeatable. Finally, the proposed electrochemical sensor was successfully applied to the determination of oleuropein in an olive leaf extract. Microwave-assisted extraction of oleuropein had good recovery values between 92% and 98%. The results obtained with the proposed electrochemical sensor were compared with liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis.

  8. Ammonia stripping, activated carbon adsorption and anaerobic biological oxidation as process combination for the treatment of oil shale wastewater.

    Science.gov (United States)

    Alexandre, Verônica M F; do Nascimento, Felipe V; Cammarota, Magali C

    2016-10-01

    Anaerobic biodegradability of oil shale wastewater was investigated after the following pretreatment sequence: ammonia stripping and activated carbon adsorption. Anaerobic biological treatment of oil shale wastewater is technically feasible after stripping at pH 11 for reducing the N-NH3 concentration, adsorption with 5 g/L of activated carbon in order to reduce recalcitrance and pH adjustment with CO2 so that the sulphate concentration in the medium remains low. After this pretreatment sequence, it was possible to submit the wastewater without dilution to an anaerobic treatment with 62.7% soluble chemical oxygen demand removal and specific methane production of 233.2 mL CH4STP/g CODremoved.

  9. Simultaneous determination of textile dyes by Adsorptive Cathodic Stripping Voltammetry - doi: 10.4025/actascitechnol.v35i2.16595

    National Research Council Canada - National Science Library

    Lidia Brizola Santos; Fernando Santos Domingues; Fernando Rosseto; Vitor de Cinque Almeida; Juliana Carla Garcia; Nilson Evelázio de Souza

    2013-01-01

    The Adsorptive Cathodic Stripping Voltammetry (ACSV - differential pulse) proved to be an efficient method in the separation and quantification of two reactive textile dyes, Procion Yellow (PY) and Procion Red (PR...

  10. Determination of Se(IV) in natural waters by adsorptive stripping voltammetry of 5-nitropiazselenol.

    Science.gov (United States)

    Ashournia, Mehdi; Aliakbar, Alireza

    2010-02-15

    The high tendency of 5-nitropiazselenol for self-accumulation on thin mercury film electrode was used innovatively for determination of Se(IV) in natural waters. 5-Nitropiazselenol was formed by reaction between Se(IV) and 4-nitro-1,2-phenylenediamine in acidic solution and self-accumulation process was carried out directly from reaction media. The adsorbed 5-nitropiazselenol was stripped in HCl solution by DP cathodic potential scan. All parameters influencing the measurement were optimized and evaluated. Detection limit of this method is 0.06 ng mL(-1). Interferences of various cations and anions were studied. The adsorption tendency of some other piazselenols made by some aromatic ortho-diamines was also investigated. The problems arising from applying potential during accumulation process in natural waters analysis were discussed. This method was applied for determination of Se(IV) in natural waters collected from some internationally registrated lagoons south of Caspian Sea. The obtained results were compared with the results of ICP-AES and DPCSV after electrochemical preconcentration.

  11. Determination of copper speciation in highway stormwater runoff using competitive ligand exchange - Adsorptive cathodic stripping voltammetry.

    Science.gov (United States)

    Nason, Jeffrey A; Sprick, Matthew S; Bloomquist, Don J

    2012-11-01

    Low concentrations of dissolved copper have been shown to adversely affect the olfactory system of salmonid species, impairing their ability to avoid predators and likely increasing mortality. These studies have resulted in increased regulatory scrutiny of stormwater discharges to surface waters inhabited by threatened and endangered salmonid species. Because it is primarily the free ionic (Cu(2+)) and weakly complexed forms of copper that are bioavailable, it is critical to understand the speciation of copper in stormwater. This paper reports on the characterization of copper binding ligands and copper speciation in composite samples of highway stormwater runoff collected at four sites in Oregon, USA using competitive ligand exchange - adsorptive cathodic stripping voltammetry (CLE-ACSV). Although the concentration and strength of copper binding ligands in stormwater varied considerable between sites and storms, the vast majority (>99.9%) of the total dissolved copper in composite samples was complexed by organic ligands in stormwater. Although total dissolved copper concentrations range from 2 to 20 μg/L, the analytically determined free ionic copper concentrations did not exceed 10(-10) M (6.3 ng/L) in any of the fully characterized samples, suggesting that much of the copper in highway stormwater is not bioavailable. Analytically determined free ionic copper concentrations were compared with those predicted by a readily available chemical equilibrium models and found to be in reasonable agreement. Copyright © 2012 Elsevier Ltd. All rights reserved.

  12. Quantification of sub-nanomolar levels of Penicillin G by differential pulse adsorptive stripping voltammetry.

    Science.gov (United States)

    Abbasi, S; Khodarahmian, K; Farmany, A

    2012-02-01

    A novel selective and sensitive method is developed for determination of Penicillin G by Differential Pulse Adsorptive Stripping Voltammetry (DPAdSV). Penicillin G gave well-resolved diffusion-controlled cathodic peaks at -0.42 and -0.584 V, respectively (vs Ag/AgCl) in pH 7.50 of borate buffer. Optimal conditions were obtained as pH 7.50, accumulation potential of -0.2 V (vs Ag/AgCl), accumulation time of 120 s, and scan rate of 100 mV/s. Under the optimized conditions, a linear calibration curve was established for the concentration of Penicillin G in the range of 0.007-2.13 µg/ml with a detection limit of 0.000717 µg/ml. The procedure was successfully applied to the determination of Penicillin G in various medicine and biological samples. The relative standard deviation of the method at 0.05 and 0.5 µg/ml Penicillin G, for 10 runs, was 2.55% and 2.06%, respectively. Copyright © 2011 John Wiley & Sons, Ltd.

  13. ADSORPTIVE VOLTAMMETRIC BEHAVIOR OF LOMEFLOXACIN AND ITS APPLICATION%洛美沙星的吸附伏安特性及其应用

    Institute of Scientific and Technical Information of China (English)

    曹尔新; 曾泳淮; 高红艳

    2001-01-01

    在Britton-Robinson(pH8.80)-0.02mol*L-1 KCl底液中,洛美沙星(Lomefloxacin,简称LMF)在汞电极上有一线性扫描还原峰,峰电位Ep=-1.40V (vs.Ag/AgCl),该峰具有明显的吸附性.吸附粒子为LMF中性分子,测得LMF在汞电极上的饱和吸附量Гs=4.27×10-11 mol*cm-2,每个LMF分子所占电极面积为3.89nm2,LMF在汞电极上的吸附符合Langmuir吸附等温式.测得吸附系数β=2.29×106,25℃时的吸附自由能ΔG=-36.29kJ*mol-1,电极反应电子数n=2,不可逆体系动力学参数αnα=1.84,表面电极反应速率常数ks=0.29s-1,扩散系数D=7.38×10-7 cm2*s-1.建立了吸附溶出伏安法测定LMF的最佳条件,检出限为5.0×10-8 mol*L-1.%In a supporting electrolyte containing Britton-Robinson (pH8.80)-0.02mol*L-1 KCl , a reduction peak of LMF is observed by linear-sweep voltammetry at Hg electrode. The peak shows a potential of -1.40V(vs.Ag/AgCl) and adsorptive characteri-stics. The adsorbed species is most probably the neutral molecular of LMF. The saturated adsorption amount of LMF at Hg electrode is 4.27×10-11 mol*cm-2 and every LMF molecule occupies an area of 3.89nm2. On the surface of the hanging mercury drop electrode, the adsorption of LMF obeys Langmuir adsorption isotherm. The adsorption coefficient β is 2.29×106, the Gibbs energy of adsorption ΔG is -36.29kJ*mol-1, the number of electrons transferred n is 2, the kinetics parameter αnα is 1.84, the rate constant ks of surface electrode reaction is 0.29s-1, and the diffusion coefficient D is 7.38×10-7 cm2*s-1. The detection limit of the adsorptive stripping voltammetry of LMF is 5.0×10-8 mol*L-1under optimized condition.

  14. Stripping Voltammetric Determination Of Zinc, Cadmium, Lead And Copper In Blood Samples Of Children Aged Between 3 Months And 6 years

    Directory of Open Access Journals (Sweden)

    Rakesh Kumar Mahajan

    2005-05-01

    Full Text Available Blood samples of 160 children, ranging age between 3 months and 6 years were selected from five different parts of Amritsar district of Punjab (India and were analyzed for Zn, Cd, Pb and Cu using anodic stripping voltammetry. Large variations in the results have been correlated to the area inhabited, age differences and other factors. It was found that the areas, more prone to environmental stress, had shown more quantities of these metals in blood samples in comparison to those which were taken from safer sites. Similarly the younger children lesser exposed to environmental pollution had shown comparatively lesser quantity of these metals in comparison to older objects.

  15. Determination of trace amounts of Ga(III) by adsorptive stripping voltammetry with in situ plated bismuth film electrode.

    Science.gov (United States)

    Grabarczyk, Malgorzata; Wasąg, Joanna

    2015-11-01

    The determination of trace gallium using adsorptive stripping voltammetry at an in situ plated bismuth film electrode was described. The method was based on simultaneous film formation and the Ga(III)-cupferron complex preconcentration at -0.65 V and its cathodic stripping during the potential scan. The effect of Bi(III) and cupferron concentration, the influence of deposition potential and time, and the scan rate on the determination of Ga(III) were studied. A linear response in the concentration range of 3×10(-10) to 3×10(-7) mol L(-1) (r=0.998) was obtained with detection limit of 1.05×10(-10) mol L(-1) using accumulation time of 180 s. Finally, the bismuth film electrode was successfully applied for the determination of Ga(III) in certified reference material seawater NASS-5 with satisfactory results.

  16. Voltammetric method for the determination of sildenafil citrate (Viagra) in pure form and in pharmaceutical formulations.

    Science.gov (United States)

    Tyszczuk, Katarzyna; Korolczuk, Mieczyslaw

    2010-06-01

    A highly sensitive and simple voltammetric method for the determination of sildenafil citrate (SC) was developed. The method is based on the accumulation by adsorption of SC on a lead film modified glassy carbon electrode (LF/GCE) and then the reduction of SC throughout the stripping step. During the determinations of SC at the lead film electrode three adsorptive stripping voltammetric peaks at -1.2, -1.33 and -1.45V were observed. The respective response selected for identification and quantification has been evaluated with respect to the composition and pH of the supporting electrolyte, the potential and the time of the lead film formation, the potential and the time of the SC accumulation and other variables. Experimental results indicate an excellent linear correlation between the peak current and concentration in the range of 2x10(-9)-1.5x10(-7)mol/L (for peaks 1 and 2) and 1x10(-8)-1.5x10(-7)mol/L (for the peak 3). The detection limits (LOD) for SC following 30s of accumulation time were equal to 9x10(-10)mol/L (for peaks 1 and 2) and 4.5x10(-9)mol/L (for the peak 3). The method was successfully applied to the determination of SC in the tablets (Viagra 25 and Viagra 50) and average the contents were in close agreement with those quoted by the manufacturer and with those obtained by the reported spectrophotometric method and voltammetric method using a hanging mercury drop electrode.

  17. Sensitive Bioanalysis Based on in-Situ Droplet Anodic Stripping Voltammetric Detection of CdS Quantum Dots Label after Enhanced Cathodic Preconcentration.

    Science.gov (United States)

    Qin, Xiaoli; Wang, Linchun; Xie, Qingji

    2016-08-23

    We report a protocol of CdS-labeled sandwich-type amperometric bioanalysis with high sensitivity, on the basis of simultaneous chemical-dissolution/cathodic-enrichment of the CdS quantum dot biolabel and anodic stripping voltammetry (ASV) detection of Cd directly on the bioelectrode. We added a microliter droplet of 0.1 M aqueous HNO₃ to dissolve CdS on the bioelectrode and simultaneously achieved the potentiostatic cathodic preconcentration of Cd by starting the potentiostatic operation before HNO₃ addition, which can largely increase the ASV signal. Our protocol was used for immunoanalysis and aptamer-based bioanalysis of several proteins, giving limits of detection of 4.5 fg·mL(-1) for human immunoglobulin G, 3.0 fg·mL(-1) for human carcinoembryonic antigen (CEA), 4.9 fg·mL(-1) for human α-fetoprotein (AFP), and 0.9 fM for thrombin, which are better than many reported results. The simultaneous and sensitive analysis of CEA and AFP at two screen-printed carbon electrodes was also conducted by our protocol.

  18. Sensitive Bioanalysis Based on in-Situ Droplet Anodic Stripping Voltammetric Detection of CdS Quantum Dots Label after Enhanced Cathodic Preconcentration

    Directory of Open Access Journals (Sweden)

    Xiaoli Qin

    2016-08-01

    Full Text Available We report a protocol of CdS-labeled sandwich-type amperometric bioanalysis with high sensitivity, on the basis of simultaneous chemical-dissolution/cathodic-enrichment of the CdS quantum dot biolabel and anodic stripping voltammetry (ASV detection of Cd directly on the bioelectrode. We added a microliter droplet of 0.1 M aqueous HNO3 to dissolve CdS on the bioelectrode and simultaneously achieved the potentiostatic cathodic preconcentration of Cd by starting the potentiostatic operation before HNO3 addition, which can largely increase the ASV signal. Our protocol was used for immunoanalysis and aptamer-based bioanalysis of several proteins, giving limits of detection of 4.5 fg·mL−1 for human immunoglobulin G, 3.0 fg·mL−1 for human carcinoembryonic antigen (CEA, 4.9 fg·mL−1 for human α-fetoprotein (AFP, and 0.9 fM for thrombin, which are better than many reported results. The simultaneous and sensitive analysis of CEA and AFP at two screen-printed carbon electrodes was also conducted by our protocol.

  19. Cathodic stripping voltammetric determination of As(III) with in situ plated bismuth-film electrode using the catalytic hydrogen wave.

    Science.gov (United States)

    Jiajie, Long; Nagaosa, Yukio

    2007-06-12

    A highly sensitive method has been developed for the determination of trace As(III) by a square wave cathodic stripping voltammetry employing in situ plated bismuth-film on edge-plane graphite substrate as working electrode. The presence of As(III) enhanced a cathodic peak corresponding to the catalytic hydrogen wave due to Se(IV) at about -1150 mV. Linear calibration curves for As(III) determination were obtained over the concentration ranges of 0.01-1.0 microg L(-1) and 1.0-12.0 microg L(-1) at deposition times of 30 s and 10 s, respectively. The detection limit (3sigma) was estimated to be as low as 0.7 ng L(-1) As(III) at 30 s deposition time. The optimum experimental parameters and probable interference from foreign ions and organic compounds were investigated. This proposed method could be applied to analyses of certified reference material, synthetic and natural water samples.

  20. Simultaneous determination of ultra trace amounts of lead and cadmium in food samples by adsorptive stripping voltammetry.

    Science.gov (United States)

    Abbasi, Shahryar; Khodarahmiyan, Kobra; Abbasi, Freshteh

    2011-09-01

    A selective and sensitive method for simultaneous determination of lead and cadmium by adsorptive differential pulse cathodic stripping voltammetry is presented. The method is based on adsorptive accumulation of the complexes of Pb (II) and Cd (II) ions with 2-mercaptobenzothiazole onto hanging mercury drop electrode (HMDE), followed by the reduction of the adsorbed species by differential pulse cathodic stripping voltammetry. Optimal conditions were obtained at pH 8.0, 2-mercaptobenzothiazole concentration of 1.0×10(-4)M, the accumulation potential of -0.4V (vs. Ag/AgCl), the accumulation time of 160s, and the scan rate of 100mV/s. Under optimised conditions, linear calibration curves were established for the concentration of Pb (II) and Cd (II) in the range of 0.5-70 and 0.2-30ng/ml, respectively, with detection limit of 0.017ng/ml for Pb (II) and 0.01ng/ml for Cd (II). The procedure was successfully applied to the simultaneous determination of both ions in food samples (rice, soya and sugar). Published by Elsevier Ltd.

  1. Construction of an electrochemical sensor based on amino-functionalized metal-organic frameworks for differential pulse anodic stripping voltammetric determination of lead.

    Science.gov (United States)

    Wang, Yang; Ge, Huali; Wu, Yichun; Ye, Guiqin; Chen, Huanhuan; Hu, Xiaoya

    2014-11-01

    Metal-organic frameworks composite materials have received tremendous attention because of their versatile structures and tunable porosity for various applications. Herein, amino-functionalized metal-organic frameworks (NH2-Cu3(BTC)2; BTC=benzene-1,3,5-tricarboxylate) was prepared and used as a novel electrode modifier for the determination of trace levels of lead. NH2-Cu3(BTC)2 shows quite a good capability for the efficient adsorption of lead from aqueous solutions. The parameters affecting the electrochemical process, such as electrolyte solution pH, the amount of NH2-Cu3(BTC)2 suspension, accumulation potential and accumulation time, were investigated in detail. Under the optimal conditions, the electrochemical sensor exhibited a linear response to the concentration of lead in the range of 1.0×10(-8)-5.0×10(-7) mol L(-1) (R(2)=0.9951) with a detection limit of 5.0×10(-9) mol L(-1). The relative standard deviation of 11 successive scans was 3.10% for 1.0×10(-8) mol L(-1) lead. The method was validated with certified reference material (stream sediment and milk powder) and the analytical results coincided well with the certified values. Furthermore, the method was successfully applied to the determination of target analytes in tap and lake water samples and good recoveries were obtained from different spiked values.

  2. Differential pulse and square-wave cathodic stripping voltammetry of xanthine and xanthosine at a mercury electrode.

    Science.gov (United States)

    Temerk, Y M; Kamal, M M; Ahmed, G A W; Ibrahim, H S M

    2003-08-01

    The surface activity of xanthine (Xan) and xanthosine (Xano) at a hanging mercury drop electrode (HMDE) was studied using out-of-phase ac and cyclic dc voltammetry. The results show that Xan and Xano were strongly adsorbed and chemically interacted with the charged mercury surface, which is the prerequisite step for applying the cathodic adsorptive stripping voltammetric determination of such biologically important compounds. Differential pulse cathodic adsorptive stripping voltammetry (DPCASV) and square-wave cathodic adsorptive stripping voltammetry (SWCASV) were applied for the ultratrace determination of Xan and Xano compounds. Moreover, a rapid and sensitive controlled adsorptive accumulation of Cu(II) complexes of both compounds provided the basis of a direct stripping voltammetric determination of such compounds to submicromolar and nanomolar levels. Operational and solution conditions for the quantitative ultratrace determination of Xan and Xano were optimized in absence and presence of Cu(II). The calibration curve data were subjected to least-squares refinements. The effects of several types of inorganic and organic interfering species on the determination of Xan or Xano were considered.

  3. Determination of triazines in hemodialysis saline solutions by adsorptive stripping voltammetry after extraction in acetonitrile

    Directory of Open Access Journals (Sweden)

    Nascimento Paulo Cícero do

    2003-01-01

    Full Text Available A method for the voltammetric determination of 2-methylthio-4,6-dialkylamino-1,3,5-triazine (triazines herbicides in hemodialysis (HD saline solutions was developed. The herbicides were detected in the saline solutions at the hanging mercury drop electrode (HMDE with high sensitivities only after extraction of the analytes in acetonitrile (ACN. The salting out effect originated by the saline environment existing in the solutions enabled the extractions. The volume ratio between the saline and ACN phases was investigated in order to find the best sensitivity to detect the triazines. The speciation amongst them (ametryn, desmetryn, prometryn and terbutryn was not possible. Recoveries between 88 and 107% were calculated in spiked samples, and detection limits of 0.03 mumol L-1 were calculated for the triazines in the saline samples using this methodology.

  4. 基于表面活性剂存在下电化学结合化学计量学同时测定3种着色剂%Simultaneous differential pulse stripping voltammetric determination of three food colorants in presence of CTAB with aid of chemometrics

    Institute of Scientific and Technical Information of China (English)

    钟永生; 桂怿; 倪永年

    2012-01-01

    利用微分脉冲伏安法研究了日落黄、苋菜红和柠檬黄等3种着色剂在裸玻碳电极上的电化学行为及定量分析测定的可行性.实验发现,在表面活性剂溴化十六烷基三甲铵(CTAB,浓度为40.0×10-6 mol·L-1)存在下,3种着色剂日落黄、苋菜红和柠檬黄均具有较高的电化学测定灵敏度,它们的线性范围分别为4.0~40.0,5.0~60.0和2.5~35.0 nmol·L-1,对应的最低检测线分别为1.54,2.38和1.10 nmol·L-1.但这3种被测物质中日落黄和苋菜红的伏安波谱相互重叠,因此在不进行化学分离预处理的情况下很难对这3种着色剂同时进行测定.采用偏最小二乘法、主成分分析以及它们的一阶导数等化学计量学方法对它们的重叠伏安谱图进行解析和定量分析,结果表明,导数偏最小二乘法的计算结果最好,总相对预测误差(RPET)为6.18%.利用提出的方法对冰激凌、汽水和糖果等实际样中的3种着色剂进行直接测定,获得了较好的定量分析结果.%The differential pulse stripping voltammetric (DPSV) method was developed, to determine hree colorants,sunset yellow,amaranth and tartrazine. The method proposed was based on the adsorptive accumulation of the colorants on the carbon electrode,and the oxidation of the absorptive species by the voltam-metry. The 40. 0×10-6 mol · L-1 of cetyltrimethyl ammonium bromide (CTAB) was used as the optimal for the experiment. The linear concentration ranges were found to be 4. 0-40. 0.5. 0-60. 0 and 2. 5-35. 0 nmol · L-1 ,for sunset yellow, amaranth and tartrazine, respectively. Their corresponding detection limits were 1. 54,2. 38 and 1. 10 nmol · L-1. Since the voltammograms of these colorants were seriously overlapped, it was difficult to determine them individually from the voltammetric signals of the mixtures. Thus, some chemometrics methods,such as partial least squares (PLS),principle component regression (PCR) and their first-order derivative

  5. Adsorptive stripping chronopotentiometry (AdSCP). Part 2: Basic experimental features

    NARCIS (Netherlands)

    Leeuwen, van H.P.; Town, R.M.

    2007-01-01

    AdSCP determines a metal ion, M, by reaction with added ligand, Lad, to form a surface active MLad which is accumulated on an electrode surface, then quantified by constant current reduction. The chronopotentiometric stripping curves for Pb(II), with xylenol orange (XO) as the added ligand, are scru

  6. Differential pulse voltammetric determination of P(V) following adsorptive accumulation of alpha-[PMo(12)O(40)](3-) on a polypyrrole-modified glassy carbon electrode.

    Science.gov (United States)

    Takamoto, Masayo; Himeno, Sadayuki

    2003-03-01

    On the basis of the formation and pre-concentration of an alpha-Keggin-type [PMo(12)O(40)](3-) complex, a novel voltammetric method was developed for the determination of trace levels of P(V). The alpha-[PMo(12)O(40)](3-) complex was formed by heating a 5x10(-4) M Mo(VI)-0.2 M HCl-40% (v/v) CH(3)CN system containing a trace amount of P(V) at 70 degrees C for 30 min. During the electrochemical polymerization of pyrrole in the alpha-[PMo(12)O(40)](3-) solution, the alpha-[PMo(12)O(40)](3-) complex was accumulated into the polypyrrole film on a glassy carbon electrode. The differential pulse voltammetric peak current due to the alpha-[PMo(12)O(40)](3-) complex incorporated in the polypyrrole film was linearly dependent on the P(V) concentration in the range of 5x10(-9)-5x10(-7) M; a detection limit of 2x10(-9) M was achieved.

  7. Extending the dynamic range of copper determination in differential pulse adsorption cathodic stripping voltammetry using wavelet neural network.

    Science.gov (United States)

    Khayamian, T; Ensafi, Ali A; Benvidi, A

    2006-07-15

    A wavelet neural network (WNN) model is proposed for extending the dynamic range of Cu(II) determination by differential pulse adsorption cathodic stripping voltammetry (DP-AdSV) using xylenol orange (XO) as a suitable ligand. All of voltammograms data consisting of Cu(II) and Cu(II)-XO peak currents were used in WNN model. The WNN model consisted of three layers (2-8-1) with the Morlet mother wavelet transfer function in the hidden layer. The model was able to extend the dynamic range of Cu(II) from its narrow linear range (1-50 ng ml(-1)) to the higher dynamic range (1-1500 ng ml(-1)). The results of the WNN model was also compared with artificial neural network (ANN) model and it was demonstrated the superiority of the WNN model relative to ANN model.

  8. Application of adsorptive stripping voltammetry to the simultaneous determination of bismuth and copper in the presence of nuclear fast red.

    Science.gov (United States)

    Gholivand, M B; Romiani, A A

    2006-06-30

    A sensitive and selective method for the simultaneous determination of copper and bismuth by adsorptive stripping was developed using nuclear fast red (2-anthracenesulfonic acid, 4-amino-9,10-dihydro-1,3-dihydroxy-9,10-dioxo-, monosodium salt) as selective complexing agent onto hanging mercury drop electrode. In a single scan both metals gave peaks that were distinctly separated by 85 mV allowing their determination in the presence of each other. Optimal analytical conditions were found to be: nuclear fast red concentration of 80 microM, pH of 2.8 and adsorptive potential of -300 mV versus Ag/AgCl. With accumulation time of 180s the peaks currents are proportional to concentration of copper and bismuth over the 1-100 and 5-60 ng mL(-1) range with detection limits of 0.2 and 1.2 ng mL(-1), respectively. The procedure was applied to simultaneous determination of copper and bismuth in some real samples.

  9. Applicability of 2-hydroxybenzaldehyde benzoylhydrazone in the determination of trace metals by adsorptive cathodic stripping voltammetry: relevancy of simultaneous determinations.

    Science.gov (United States)

    Espada-Bellido, Estrella; Galindo-Riaño, M Dolores; Aouarram, Abdellah; García-Vargas, Manuel

    2009-07-01

    The applicability of 2-hydroxybenzaldehyde benzoylhydrazone (2-HBBH) for determining Cd(II), Cu(II), Pb(II) and Bi(III) ions by adsorptive cathodic stripping voltammetry was studied. The sensitivity of metal reduction peak currents was highly enhanced with the addition of 2-HBBH to metallic solutions, showing the adsorptive characteristics of the complexes. Variable factors affecting the response (mainly: the influences of pH, supporting electrolyte and deposition potential on selectivity and sensitivity) were investigated. Limits of detection suitable for trace analysis were obtained: 0.28 microg L(-1) for Cd(II) at pH 10; 0.026 microg L(-1) for Pb(II) at pH 9; 0.285 microg L(-1) for Bi(III) at pH 8 and 0.051 microg L(-1) for Cu(II) at pH 9.5. Simultaneous determinations of two groups of elements, consisting of Cd(II)-Pb(II)-Cu(II) and Cd(II)-Pb(II)-Bi(III), at pH 9.5 and 9, respectively, were described with good resolution and sensitivities. Metals were quantified at concentrations in the range from 0.5 to 14 microg L(-1). The RSD at a concentration level of 5 microg L(-1) of metal was 4.28% for Cd(II), 2.99% for Pb(II), 4.82% for Bi(III) and 1.35% for Cu(II). The method was applied to the simultaneous determination of metals in certified reference water (TMDA-62) and in synthetic water samples with satisfactory results.

  10. Determination of Cr (in small quantities) by adsorptive stripping voltammetry: a comparative study of square wave versus differential pulse

    Energy Technology Data Exchange (ETDEWEB)

    Misiego, A.Sanchez; Carra, R.M.Garcia-Monco; Carracedo, P.Ambel; Torre, M.E.Majado [Departamento de Quimica Analitica y Electroquimica, Universidad de Extremadura, 06071, Badajoz (Spain)

    2003-08-01

    The usefulness of an analytical method must be measured according to its practical application possibilities. A comparative study has been carried out here between the SW (working in an open atmosphere) and DP (working with de-aerated solutions) variants of catalytic-stripping adsorptive voltammetry applied to the determination of chromium traces in triethylenetetraminehexaacetic acid (TTHA) medium. In order to optimise the analytical signal, accumulation potential, nitrate ion concentration, pH, and TTHA concentration parameters were evaluated. Four linearity ranges were established within the interval 0.5-2000 nmol L{sup -1} chromium concentration in the cell, each with the recommended accumulation time. Quality parameters such as repeatability, linear regression, validity limits, precision, and sensitivity were evaluated. The SW variant is significantly advantageous when the chromium concentration in cell is less than 10 nmol L{sup -1} and even more if analysis time, cost, and being able to work in an open atmosphere are considered. The results are comparable to those obtained using GTAAS. Employing a CRM (tomato leaves), the accuracy is 1-4%. The proposed procedure, using tree leaves as samples, has been successfully tested for the possible monitoring of chromium contamination of the atmosphere. (orig.)

  11. The cyclic renewable mercury film silver based electrode for determination of molybdenum(VI) traces using adsorptive stripping voltammetry.

    Science.gov (United States)

    Piech, Robert; Baś, Bogusław; Kubiak, Władysław W

    2008-07-15

    The new cyclic renewable mercury film silver based electrode (Hg(Ag)FE), applied for the determination of molybdenum(VI) traces using differential pulse adsorptive cathodic stripping voltammetry (DP AdSV) is presented. The Hg(Ag)FE electrode is characterized by very good surface reproducibility (

  12. Simultaneous determination of trace uranium(VI) and zinc(II) by adsorptive cathodic stripping voltammetry with aluminon ligand.

    Science.gov (United States)

    Cha, K W; Park, C I; Park, S H

    2000-09-05

    Uranium(VI) complexed with aluminon (3-[bis(3-carboxy-4-hydroxy-phenyl)methylene]-6-oxo-1,4-cyclohexadiene-1-carboxylic acid triammonium salt) was determined by adsorptive cathodic stripping voltammetry (ACSV) using a hanging mercury drop electrode. Trace uranium(VI) and zinc(II) can be simultaneously determined in a single scan in the presence of aluminon and urea. Optimal conditions were found to be: accumulation time; 180-200 s, accumulation potential; 50 mV versus Ag/AgCl, scan rate; 40 mV s(-1), supporting electrolyte; 0.1 M sodium acetate buffer at pH 6.5-7.0, and concentration of aluminon; 1x10(-6) M. The linear range of uranium(VI) and zinc(II) were observed over the concentration range 2-33 and 30-120 ng ml(-1), respectively. The detection limit (S/N=3) are 0.2 ng ml(-1) (uranium) and 30 ng ml(-1) (zinc). A good reproducibility shows RSDs of 2.5-4.0% (n=10). The procedure offers high selectivity, with the presence of urea masking some metal ions.

  13. Unprecedented stable aqueous semiquinone methide radical formation interferes with adsorptive cathodic stripping voltammetry of cobalt methyl thymol blue.

    Science.gov (United States)

    Niztayev, Alidin N; Hagen, Wilfred R

    2005-09-15

    A putatively highly sensitive and selective method for the determination of cobalt in aqueous samples by catalytic adsorptive cathodic stripping voltammetry using methyl thymol blue (MTB) as the ligand has been documented [A. Safavi, E. Shams, Talanta 51 (2000) 1117] and its underlying mechanism has been briefly explored [A. Safavi, E. Shams, Electroanalysis 14 (2002) 708]. In an attempt to adapt the method for application in metalloprotein analysis we obtained erratic results, which were traced down to the redox non-innocence of the free ligand in the potential range prescribed for the metal analysis. On the hanging mercury drop electrode free methyl thymol blue is reversibly one-electron reduced to the semiquinone form with E(m,7.0)=-482mV versus NHE at 22 degrees C, and the radical is subsequently quasi-reversibly one-electron reduced to the quinol form with E(m,7) approximately -0.9V. This observation invalidates the use of MTB in electrochemical analysis of metal ions. This is also the first observation ever of a stable quinone methide radical in aqueous solution.

  14. Determination of ultra trace amount of enrofloxacin by adsorptive cathodic stripping voltammetry using copper(II) as an intermediate.

    Science.gov (United States)

    Ensaifi, Ali A; Khayamian, T; Taei, M

    2009-05-15

    In this work, a simple and sensitive electroanalytical method was developed for the determination of enrofloxacin (ENRO) by adsorptive cathodic stripping voltammetry (ADSV) using Cu(II) as a suitable probe. The complex of copper(II) with ENRO was accumulated at the surface of a hanging mercury drop electrode at -0.10 V for 40 s. Then, the preconcentrated complex was reduced and the peak current was measured using square wave voltammetry (SWV). The optimization of experimental variables was conducted by experimental design and support vector machine (SVM) modeling. The model was used to find optimized values for the factors such as pH, Cu(II) concentration and accumulation potential. Under the optimized conditions, the peak current at -0.30 V is proportional to the concentration of ENRO over the range of 10.0-80.0 nmol L(-1) with a detection limit of 0.33 nmol L(-1). The influence of potential interfering substances on the determination of ENRO was examined. The method was successfully applied to determination of ENRO in plasma and pharmaceutical samples.

  15. Electrochemistry and determination of cefdinir by voltammetric and computational approaches

    Directory of Open Access Journals (Sweden)

    İbrahim Hüdai Taşdemir

    2014-12-01

    Full Text Available The oxidation and reduction behavior of cefdinir (CEF was studied by experimental methods and computational calculations at B3LYP/6-31+G (d//AM1. Voltammetric studies were carried out based on two irreversible reduction peaks at approximately −0.5 and −1.2 V on a hanging mercury drop electrode (HMDE and on one irreversible oxidation peak at approximately 1.0 V on a glassy carbon electrode (GCE versus Ag/AgCl, KCl (3.0M in Britton–Robinson (BR buffer at pH 4.2 and 5.0, respectively. Differential pulse adsorptive stripping voltammetric methods have been developed and validated for determination of CEF in different samples. The linear range was established as 0.25–40.0 μM for HMDE and 0.40–10.0 μM for GCE. Limit of quantification was calculated to be 0.20 and 0.26 μM for HMDE and GCE, respectively. These methods were successfully applied to assay the drug in tablets and human serum with good recoveries between 92.7% and 107.3% having relative standard deviation less than 10%.

  16. Overlapping voltammetric peaks - an analytical procedure for simultaneous determination of trace metals. Application to food and environmental matrices

    Energy Technology Data Exchange (ETDEWEB)

    Locatelli, Clinio [University of Bologna, Department of Chemistry, G. Ciamician, Bologna (Italy); University of Bologna, CIRSA (Centro Interdipartimentale di Ricerca per le Scienze Ambientali - Interdepartment Centre for Research in Environmental Sciences), Laboratory of Environmental Analytical Chemistry, Ravenna (Italy)

    2005-03-01

    Voltammetric methods are very suitable, versatile and rapid techniques for simultaneous determination of metals in complex matrices. The present work, determination of Cu(II), Sn(II), Sb(III), Tl(I), and Pb(II) by square-wave anodic-stripping voltammetry and Cr(VI) by square-wave adsorptive-stripping voltammetry, is an interesting example of the possibility of simultaneous determination of each single element in food and environmental samples, even in the presence of reciprocal interference. Dibasic ammonium citrate, pH 6.3 or 8.2, was employed as supporting electrolyte. The voltammetric measurements were carried out using a stationary hanging mercury drop electrode as working electrode and a platinum electrode and an AgAgClKCl{sub sat} electrode as auxiliary and reference electrodes, respectively. The analytical procedure was verified by analysis of standard reference materials - wholemeal BCR-CRM 189, wheat flour NIST-SRM 1567a, rice flour NIST-SRM 1568a, estuarine sediment BCR-CRM 277, river sediment BCR-CRM 320, and Montana soil with moderately elevated traces NIST-SRM 2711. Precision and accuracy, expressed as relative standard deviation and relative error, respectively, were generally below 6% whereas limits of detection for each element were below 0.069 {mu}g g{sup -1}. In the presence of reciprocal interference the standard addition method considerably improved the resolution of the voltammetric technique, even for very high element concentration ratios. After being set up on the standard reference materials the analytical procedure was transferred and applied to commercial samples of meal and soil samples taken from sites devoted to agricultural practice. A critical comparison with graphite furnace atomic-absorption spectroscopy is also discussed. (orig.)

  17. Determination of platinum-group metals and lead in vegetable environmental bio-monitors by voltammetric and spectroscopic techniques: critical comparison.

    Science.gov (United States)

    Locatelli, Clinio; Melucci, Dora; Torsi, Giancarlo

    2005-08-01

    This paper reports voltammetric sequential determination of Pt(II), Pd(II), and Rh(III), by square-wave adsorption stripping voltammetry (SWAdSV), and Pb(II), by square-wave anodic stripping voltammetry (SWASV), in vegetable environmental matrices. Analytical procedures were verified by the analysis of the standard reference materials: Olive Leaves BCR-CRM 062 and Tomato Leaves NIST-SRM 1573a. Precision and accuracy, expressed as relative standard deviation and relative error, respectively, were always less than 6% and the limits of detection (LOD) for each element were below 0.096 mug g(-1). Once set up on the standard reference materials, the analytical procedure was transferred and applied to laurel leaves sampled in proximity to a superhighway and in the Po river mouth area. A critical comparison with spectroscopic measurements is discussed.

  18. Determination of nitrofurantoin drug in pharmaceutical formulation and biological fluids by square-wave cathodic adsorptive stripping voltammetry.

    Science.gov (United States)

    Hammam, Essam

    2002-10-15

    Nitrofurnation is an antibacterial drug. It is used in the treatment of initial or recurrent urinary tract infections caused by susceptible organisms. The cyclic voltammogram of the drug in Britton-Robinson buffers (pH 2-11) exhibited a single well-defined cathodic peak at the hanging mercury drop electrode, that due to the reduction of its nitro group to the amine stage. A fully validated, sensitive, and reproducible developed procedure was described for determination of the drug in bulk form, pharmaceutical formulation, human serum and human urine using, square-wave cathodic adsorptive stripping voltammetry. The optimal experimental parameters for the drug assay were: accumulation potential = -0.4 V (vs. Ag/AgCl/ KCl(s)), accumulation time = 40 s, frequency = 120 Hz, pulse amplitude = 50 mV and scan increment = 10 mV in Britton-Robinson buffer (pH 10). A mean percentage recovery of 100.68 +/- 0.17 (n = 5) and a detection limit of 1.32 x 10(-10) M of bulk drug were achieved. Applicability to assay of the drug in pharmaceutical formulation, human serum and human urine was studied and illustrated. The mean percentage recoveries were found as: 101.49 +/- 0.65, 103.94 +/- 0.73 and 101.98 +/- 0.52 (n = 5) in pharmaceutical formulation, human serum and human urine, respectively. Detection limits of 2.86 x 10(-10) M and 5.77 x 10(-10) M nitrofurantoin were achieved in human serum and urine, respectively. Copyright 2002 Elsevier Science B.V.

  19. Determination of tryptophan and histidine by adsorptive cathodic stripping voltammetry using H-point standard addition method.

    Science.gov (United States)

    Ensafi, Ali A; Hajian, R

    2006-11-24

    A sequential method is proposed for the determination of tryptophane and histidine by adsorptive cathodic stripping voltammetry using standard addition and H-point standard addition method (HPSAM). The complexes of copper(II) with the amino acids were accumulated onto the surface of a hanging mercury drop electrode for 60s. Then the preconcentrated complexes were reduced by square wave voltammetry and the peak currents were measured. The effect of various parameters such as pH, concentration of copper, accumulation potential, accumulation time and scan rate on the sensitivity were studied by one-at-a time and artificial neural network. Under the optimized conditions, the peak currents at about +0.05 to -0.30 V is proportional to the concentration of tryptophan and histidine over the concentration ranges of 5-220 and 100-1200 nM, respectively. Optimization of the parameters by one-at-a time showed that at accumulation potential of 0.10 V (versus Ag/AgCl reference electrode) the peak current is proportional only to the concentration of tryptophan and histidine does not have any contribution to the current. The optimization results by artificial neural network showed that at accumulation potential of -0.06 V (versus Ag/AgCl) the peak current is proportional to the both concentrations of tryptophan and histidine. Therefore, the method of H-point standard addition has been used for resolving overlap voltamograms for determination of histidine in the present of tryptophane. The method was successfully applied to the determination of tryptophan and histidine in synthetic and real samples.

  20. Determination of Sb(III) using an ex-situ bismuth screen-printed carbon electrode by adsorptive stripping voltammetry.

    Science.gov (United States)

    Rojas-Romo, Carlos; Serrano, Núria; Ariño, Cristina; Arancibia, Verónica; Díaz-Cruz, José Manuel; Esteban, Miquel

    2016-08-01

    The determination of Sb(III) on an ex-situ bismuth screen-printed carbon electrode (ex-situ BiSPCE) by means of adsorptive stripping voltammetry (AdSV) using quercetin-5'-sulfonic acid as chelating agent was optimized. The effect of different experimental parameters such pH, ligand concentration (CQSA), accumulation potential (Eacc) and accumulation time (tacc) were studied to obtain a wide linear range, the highest sensitivity and the lowest detection limit. Ex-situ BiSPCE was analytically compared with a sputtered bismuth screen-printed electrode (BispSPE) under optimal conditions. The obtained analytical parameters suggest that ex-situ BiSPCE behaves much better than BispSPE and the first was selected for this study. Optimal parameters were pH=4.6; CQSA=10.0 to 20.0×10(-6)molL(-1); Eacc=-0.5V and tacc=60s. Peak area is proportional to Sb(III) concentration up to 100.0μgL(-1) (tacc 60s) and 45.0μgL(-1) (tacc 120s) range, with detection limits of 1.2μgL(-)(1) (tacc 60s) and 0.8μgL(-1) (tacc 120s). The relative standard deviation for a Sb(III) solution (20.0μgL(-1)) was 3.9% for ten successive assays. Thus, the effect of various interfering metal ions was studied and the methodology was validated using a spiked groundwater reference material with very satisfactory results.

  1. Determination of picomolar levels of iron in seawater using catalytic cathodic stripping voltammetry.

    Science.gov (United States)

    Obata, H; van den Berg, C M

    2001-06-01

    A new procedure for the direct determination of picomolar levels of iron in seawater is presented. Cathodic stripping voltammetry (CSV) is preceded by adsorptive accumulation of the iron(III)-2,3-dihydroxynaphthalene (DHN) complex from seawater, containing 20 microM DHN at pH 8.0, onto a static mercury drop electrode, followed by reduction of the adsorbed species. The reduction current is catalytically enhanced by the presence of 20 mM bromate. Optimized conditions include a 60-s adsorption period at -0.1 V and a voltammetric scan using sampled dc modulation at 10 Hz. In these conditions, a detection limit of 13 pM iron in seawater was achieved which can be lowered further by extending the adsorption time to 300 s. The new catalytic CSV method is approximately 5 times more sensitive than existing CSV methods and was tested on samples from the Atlantic Ocean.

  2. Determination of mobile form contents of Zn, Cd, Pb and Cu in soil extracts by combined stripping voltammetry

    Energy Technology Data Exchange (ETDEWEB)

    Nedeltcheva, T. [Department of Analytical Chemistry, University of Chemical Technology and Metallurgy, 8 Kl. Ohridsi Blvd., 1756 Sofia (Bulgaria)]. E-mail: nedel@uctm.edu; Atanassova, M. [Department of Analytical Chemistry, University of Chemical Technology and Metallurgy, 8 Kl. Ohridsi Blvd., 1756 Sofia (Bulgaria); Dimitrov, J. [N. Pushkarov Institute of Soil Science and Agroecology, 7 Shosse Bankya St., 1080 Sofia (Bulgaria); Stanislavova, L. [N. Pushkarov Institute of Soil Science and Agroecology, 7 Shosse Bankya St., 1080 Sofia (Bulgaria)

    2005-01-10

    The amount of mobile forms of Zn, Pb, Cd and Cu in extracts obtained by treating soil samples with ammonium nitrate were determined by an appropriate combination of anodic and cathodic stripping voltammetry with hanging mercury drop electrode. Every analysis required three mercury drops: on the first one, zinc was determined; on the second, cadmium and lead; on the third, copper was determined. Zinc, lead and cadmium were determined by conventional differential-pulse anodic stripping voltammetry. For copper determination, adsorptive differential-pulse cathodic stripping voltammetry with amalgamation using chloride ions as a complexing agent was applied. The standard deviation of the results was from 1 to 10% depending on the metal content in the sample. Voltammetric results were in good agreement with the AAS analysis. No microwave digestion of soil extracts was necessary.

  3. Depletive stripping chronopotentiometry : a major step forward in electrochemical stripping techniques for metal ion speciation analysis

    NARCIS (Netherlands)

    Town, R.M.; Leeuwen, van H.P.

    2004-01-01

    A comparative evaluation of the utility of the various modes of stripping chronopotentiometry (SCP) for trace metal speciation analysis is presented in the broad context of stripping voltammetric techniques. The remarkable fundamental advantages of depletive SCP at scanned deposition potential (SSCP

  4. Aptasensors Based on Stripping Voltammetry

    Directory of Open Access Journals (Sweden)

    Wenjing Qi

    2016-07-01

    Full Text Available Aptasensors based on stripping voltammetry exhibit several advantages, such as high sensitivity and multi-target detection from stripping voltammetric technology, and high selectivity from the specific binding of apamers with targets. This review comprehensively discusses the recent accomplishments in signal amplification strategies based on nanomaterials, such as metal nanoparticles, semiconductor nanoparticles, and nanocomposite materials, which are detected by stripping voltammetry after suitable dissolution. Focus will be put in discussing multiple amplification strategies that are widely applied in aptasensors for small biomolecules, proteins, disease markers, and cancer cells.

  5. Kinetic and equilibrium studies for the adsorption process of cadmium(II) and copper(II) onto Pseudomonas aeruginosa using square wave anodic stripping voltammetry method

    Energy Technology Data Exchange (ETDEWEB)

    Kong Bo; Tang Biyu; Liu Xiaoying; Zeng Xiandong; Duan Haiyan [State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Hunan, Changsha 410082 (China); Luo Shenglian, E-mail: kongbo2136@163.com [State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Hunan, Changsha 410082 (China); Wei Wanzhi [State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Hunan, Changsha 410082 (China)

    2009-08-15

    A novel method for the simultaneous determination of cadmium(II) and copper(II) during the adsorption process onto Pseudomonas aeruginosa was developed. The concentration of the free metal ions was successfully detected by square wave anodic stripping voltammetry (SWASV) on the mercaptoethane sulfonate (MES) modified gold electrode, while the P. aeruginosa was efficiently avoided approaching to the electrode surface by the MES monolayer. And the anodic stripping peaks of Cd{sup 2+} and Cu{sup 2+} appear at -0.13 and 0.34 V respectively, at the concentration range of 5-50 {mu}M, the peak currents of SWASV present linear relationships with the concentrations of cadmium and copper respectively. As the determination of Cd{sup 2+} and Cu{sup 2+} was in real time and without pretreatment, the kinetic characteristics of the adsorption process were studied and all the corresponding regression parameters were obtained by fitting the electrochemical experimental data to the pseudo-second-order kinetic model. Moreover, Langmuir and Freundlich models well described the biosorption isotherms. And there were some differences in the amount of metal ion adsorbed at equilibrium (q{sub e}) and other kinetics parameters when the two ions coexisted were compared with the unaccompanied condition, which were also discussed in this paper. The proposed electrode system provides excellent platform for the simultaneous determination of trace metals in complex biosorption process.

  6. Detection of aniline at boron-doped diamond electrodes with cathodic stripping voltammetry.

    Science.gov (United States)

    Spătaru, Tanţa; Spătaru, Nicolae; Fujishima, Akira

    2007-09-15

    Boron-doped diamond (BDD) electrodes were used to investigate the possibility of detecting aniline by linear-sweep cathodic stripping voltammetry. It was found that the dimeric species (p-aminodiphenylamine and benzidine) formed by anodic oxidation of aniline during the accumulation period are involved in electrochemically reversible redox processes and, in acidic media, the shape of the stripping voltammetric response is suitable for aniline detection in the micromolar concentration range. The low background current of conductive diamond is an advantage compared to other electrode materials and allows a detection limit of 1muM. Weak adsorption properties and the extreme electrochemical stability are additional advantages of BDD and it was found that, even after long-time measurements, the electrode surface can regain its initial activity by an anodic polarization in the potential region of water decomposition.

  7. Adsorptive

    Directory of Open Access Journals (Sweden)

    Vinod Kumar Gupta

    2017-05-01

    Full Text Available This work explores the feasibility of natural fibers derived from Ficus carica plant as an alternative precursor for the preparation of activated carbon via microwave assisted H3PO4 activation. The properties of activated carbon were investigated by scanning electron microscope (SEM and Fourier transform spectroscopy (FTIR. The operational parameters, chemical impregnation ratio, microwave power and irradiation time on the carbon yield and adsorption capability were investigated. Adsorption performance of Cu(II and Ni(II onto activated carbon was investigated as a function of pH, contact time, initial metal ion concentration and temperature. The adsorption capacity of Cu(II and Ni(II onto the adsorbent was found to be 23.08 and 18.78 mg/g, respectively. Adsorption of metal ions followed second order kinetics with best fit for Fraundlich adsorption isotherm. The values of thermodynamic parameters such as enthalpy change (ΔH°, entropy change (ΔS° and free energy change (ΔG° were evaluated for the adsorption of both the metal ions. Adsorption of metal ions onto activated carbon was spontaneous and endothermic in nature. The results suggested that activated carbon developed from natural fibers successfully improved the metal ions adsorption capacity. On the basis of our findings, the adsorbent could be used as a detoxifying agent for better management of industrial effluents.

  8. Voltammetric detection of As(III) with Porphyridium cruentum based modified carbon paste electrode biosensor.

    Science.gov (United States)

    Zaib, M; Saeed, A; Hussain, I; Athar, M M; Iqbal, M

    2014-12-15

    A novel biosensor based on carbon paste electrode modified with Porphyridium cruentum biomass was developed for the determination of As(III) in contaminated water. As(III) was first biosorbed-accumulated on the electrode surface at open circuit potential and then stripped off by applying anodic scan range of -0.8 to +0.8 V using differential pulse anodic stripping voltammetric technique. The best result was obtained at pH 6.0 with 0.1M HNO3 solution as stripping medium, allowing biosorption-accumulation time of 8 min using 5% P. cruentum biomass in graphite-mineral oil paste. Linear range for As(III) detection with the modified electrode-biosensor was observed between 2.5 and 20 µg L(-1). The FTIR spectrum of P. cruentum biomass confirmed the presence of active functional groups that participate in the binding of As(III). Scanning Electron Microscopy (SEM) indulged the surface morphology of modified electrode-biosensor before and after As(III) adsorption. Similarly, Atomic Force Microscopy (AFM) showed that the average roughness of the modified electrode decreased indicating the successful incorporation of P. cruentum biomass. Efficiency of the biosensor in the presence of different interfering metal (Na(+), K(+), Ca(2+), and Mg(2+)) ions were also evaluated. The application of P. cruentum modified biosensor was successfully used for the detection of As(III) in the binary metal (Fe(3+), Mn(2+), Cd(2+), Cu(2+), Ni(2+), Hg(2+), and Pb(2+)) contaminated system. The accuracy of application of biosorption based biosensor for the detection of As(III) is as low as 2.5 µg L(-1).

  9. Simultaneous determination of textile dyes by Adsorptive Cathodic Stripping Voltammetry - doi: 10.4025/actascitechnol.v35i2.16595

    Directory of Open Access Journals (Sweden)

    Lidia Brizola Santos

    2013-04-01

    Full Text Available The Adsorptive Cathodic Stripping Voltammetry (ACSV - differential pulse proved to be an efficient method in the separation and quantification of two reactive textile dyes, Procion Yellow (PY and Procion Red (PR, each containing two azo groups as chromophores and two monochlorotriazine reactive groups, at nanomolar level. The linearity of the method obtained for each reactive dye was 30.15 – 633.15 nmol L-1 for PY in B-R buffer pH 8.0, and 62.56 – 982.291 nmol L-1 for PR in B-R buffer pH 8.0, using preconcentration at -0.1 V during 60 s.   

  10. Direct simultaneous determination of Co, Cu, Fe, Ni and V in pore waters by means of adsorptive cathodic stripping voltammetry with mixed ligands.

    Science.gov (United States)

    Santos-Echeandía, Juan

    2011-07-15

    An analytical procedure is proposed for the direct simultaneous determination in a single scan of Co, Cu, Fe, Ni and V in sediment pore waters by means of adsorptive cathodic stripping voltammetry (ACSV) with mixed ligands (DMG and catechol). Optimum conditions for the determination of these five elements were studied. Detection limits of the technique depended upon the reproducibility of the procedure blank, and were found to be 0.04 nM Co, 0.09 nM Cu, 1.29 nM Fe, 0.46 nM Ni and 2,52 nMV making the method suitable for the direct simultaneous determination of these five metals in pore waters, estuarine waters and probably coastal waters. Copyright © 2011 Elsevier B.V. All rights reserved.

  11. METHANOL REMOVAL FROM METHANOL-WATER MIXTURE USING ACTIVATED SLUDGE, AIR STRIPPING AND ADSORPTION PROCESS: COMPARATIVE STUDY

    Directory of Open Access Journals (Sweden)

    SALAM K. AL-DAWERY

    2015-12-01

    Full Text Available An experimental research has been carried out in order to examine the removal of methanol from methanol-water mixtures using three different methods; activated sludge; activated carbon and air stripping. The results showed that the methanol was totally consumed by the bacteria as quickly as the feed entered the activated sludge vessel. Air stripping process has a limited ability for removing of methanol due to strong intermolecular forces between methanol and water; however, the results showed that the percentage of methanol removed using air pressure at 0.5 bar was higher than that of using air pressure of 0.25 bar. Removal of methanol from the mixture with a methanol content of 5% using activated carbon was not successful due to the limited capacity of the of the activated carbon. Thus, the activated sludge process can be considered as the most suitable process for the treatment of methanol-water mixtures.

  12. Application of disorganized monolayer films on gold electrodes to the prevention of surfactant inhibition of the voltammetric detection of trace metals via anodic stripping of underpotential deposits: detection of copper.

    Science.gov (United States)

    Herzog, Grégoire; Arrigan, Damien W M

    2003-01-15

    Development of an approach to prevention of electrode surface fouling by surfactants in samples is demonstrated. Spontaneously adsorbed monolayer systems employing short alkyl chains and bulky end groups are used to form porous disorganized monolayers on gold electrodes. Detection of copper by stripping of underpotential deposits formed at electrodes modified with disorganized films of mercaptoethanesulfonate (MES), mercaptopropanesulfonate, mercaptoacetic acid, and mercaptopropanoic acid was possible, and to a much lesser extent at aminoethanethiol and L-cysteine films. Use of short deposition times in conjunction with linear sweep anodic stripping voltammetry allowed detection of Cu2+ ions down to 1 x 10(-6) M in sulfuric acid solution, using underpotential deposition as the deposition step of the procedure. Calibration graphs were linear in the concentration range (1-80) x 10(-6) M Cu2+ using 15-s deposition at 0.00 V versus Ag/AgCl. The surfactants Tween 20, Tween 80, and Triton X-100 were found to have no affect on detection of Cu2+ ions in the calibration curve concentration range using MES-modified gold electrodes, whereas at unmodified gold electrodes very severe attenuation of the detection capability was manifested. The average slope for all calibration curves at the MES-modified electrode in the absence and presence of the surfactants at two different concentration levels was 0.0710 +/- 0.0024 microA microM(-1); in contrast, the slope of the calibration line at uncoated gold electrodes in the presence of surfactant was 0.0268 microA microM(-1). These results indicate the excellent ability of a disorganized, porous monolayer for prevention of fouling of the electrode surface by the surfactants.

  13. Adsorption

    Directory of Open Access Journals (Sweden)

    Denis J.L. Guerra

    2016-09-01

    Full Text Available Nontronite is an important phyllosilicate with a high concentration of ferric iron in the octahedral layer. A new occurrence of Brazilian nontronite sample was used for the organofunctionalization process with 3-aminopropyltriethoxysilane. Due to the increment of basic centers attached to the pendant chains, the metal adsorption capability of the final chelating material, was found to be higher than its precursor. The ability of these materials to remove Pb2+, Mn2+, and Zn2+ from aqueous solutions was followed by a series of adsorption isotherms at room temperature and pH 6.0, in batch adsorption experiments in order to explain the adsorption mechanism. In order to evaluate the phyllosilicate samples as adsorbents in a dynamic system, a glass column was fulfilled with nontronite samples (1.5 g and it was fed with 2.1 mmol dm−3 divalent cations at pH 6.0. The energetic effects caused by metal cations adsorption were determined through calorimetric titrations. The effects of three divalent metals adsorption in the zero point of charge of each material were investigated.

  14. Determination of palladium(II) with alpha-(2-benzimidazolyl)-alpha',alpha''-(N-5-nitro-2-pyridylhydrazone)-toluene by adsorptive cathodic stripping voltammetry.

    Science.gov (United States)

    Kim, Sung-Ii; Cha, Ki-Won

    2002-06-10

    The determination of palladium(II) complexed with alpha-(2-benzimidazolyl)-alpha',alpha''-(N-5-nitro-2-pyridylhydrazone)-Toluene (BINPHT) was investigated by adsorptive cathodic stripping voltammetry using hanging mercury drop electrode. Palladium(II) in the sample solution can be determined in BINPHT and ethylenediaminetetraacetic acid (EDTA). Accumulation is achieved by adsorption of Pd(II)-BINPHT complex on a hanging mercury drop electrode. Optimal conditions were found to be: supporting electrolyte; 0.01 M sodium acetate buffer at pH 5.0, accumulation potential; -590 mV versus Ag/AgCl, accumulation time; 180 s, scan rate; 50 mV s(-1), concentration of BINPHT; 2x10(-5) M. The linear range of Pd(II) was observed over the concentration range 20-100 ng ml(-1) The detection limit (S/N=3) is 2 ng ml(-1). A good reproductivity shows RSD of 2.0% (n=7). This procedure offers high selectivity with the presence of EDTA masking some metallic ions. River water sample spiking with palladium was determined.

  15. Square wave anodic stripping voltammetric determination of Cd²⁺ and Pb²⁺ at bismuth-film electrode modified with electroreduced graphene oxide-supported thiolated thionine.

    Science.gov (United States)

    Li, Zou; Chen, Li; He, Fang; Bu, Lijuan; Qin, Xiaoli; Xie, Qingji; Yao, Shouzhuo; Tu, Xinman; Luo, Xubiao; Luo, Shenglian

    2014-05-01

    Graphene oxide (GO)-thionine (TH) nanocomposite was prepared by π-π stacking. The nanocomposite was cast-coated on a glassy carbon electrode (GCE) to prepare an electroreduced GO (ERGO)-TH/GCE, then 2-mercaptoethanesulfonate (MES) was covalently tethered to ERGO-TH by potentiostatic anodization to form an ERGO-TH-MES/GCE. The thiolation reaction was monitored by electrochemical quartz crystal microbalance (EQCM). Square wave anodic stripping voltammetry (SWASV) was used to determine Cd(2+) and Pb(2+) at the ERGO-TH-MES/GCE further modified with Nafion and Bi. Under the optimal conditions, the linear calibration curves for Cd(2+) and Pb(2+) are from 1 to 40 μg L(-1), with limits of detection (S/N=3) of 0.1 μg L(-1) for Cd(2+) and 0.05 μg L(-1) for Pb(2+), respectively. The electrode was used for the simultaneous analysis of Cd(2+) and Pb(2+) in water samples with satisfactory recovery.

  16. Determination of humic substances in natural waters by cathodic stripping voltammetry of their complexes with iron.

    Science.gov (United States)

    Laglera, Luis M; Battaglia, Gianluca; van den Berg, Constant M G

    2007-09-05

    A new voltammetric method is presented for the measurement of humic substances (HS) in natural waters. The method is based on catalytic cathodic stripping voltammetry (CSV) and makes use of adsorptive properties of iron-HS complexes on the mercury drop electrode at natural pH. A fulvic acid standard (IHSS) was used to confirm the voltammetric response (peak potential and sensitivity) for the HS for natural water samples. Optimized conditions included the linear-sweep mode, deposition at -0.1 V, pH buffered at 8 and a scan rate of 50 mV s(-1). At a deposition time of 240 s in the presence of 10 nM iron and 30 mM bromate, the detection limit was 5 microg L(-1) HS in seawater, which could be lowered further by an increase in the bromate concentration, or in the adsorption time. The method was used to determine HS in the Irish Sea which were found to occur at levels between 60 and 600 microg L(-1). The new method is sufficiently sensitive to detect the low HS content in oceanic samples and has implications to the study of iron speciation.

  17. Square wave adsorptive cathodic stripping voltammetry automated by sequential injection analysis Potentialities and limitations exemplified by the determination of methyl parathion in water samples.

    Science.gov (United States)

    dos Santos, Luciana B O; Masini, Jorge C

    2008-01-14

    This paper describes the development and evaluation of a sequential injection method to automate the determination of methyl parathion by square wave adsorptive cathodic stripping voltammetry exploiting the concept of monosegmented flow analysis to perform in-line sample conditioning and standard addition. Accumulation and stripping steps are made in the sample medium conditioned with 40 mmolL(-1) Britton-Robinson buffer (pH 10) in 0.25 molL(-1) NaNO3. The homogenized mixture is injected at a flow rate of 10 microLs(-1) toward the flow cell, which is adapted to the capillary of a hanging drop mercury electrode. After a suitable deposition time, the flow is stopped and the potential is scanned from -0.3 to -1.0V versus Ag/AgCl at frequency of 250 Hz and pulse height of 25 mV. The linear dynamic range is observed for methyl parathion concentrations between 0.010 and 0.50 mgL(-1), with detection and quantification limits of 2 and 7 microgL(-1), respectively. The sampling throughput is 25 h(-1) if the in line standard addition and sample conditioning protocols are followed, but this frequency can be increased up to 61 h(-1) if the sample is conditioned off-line and quantified using an external calibration curve. The method was applied for determination of methyl parathion in spiked water samples and the accuracy was evaluated either by comparison to high performance liquid chromatography with UV detection, or by the recovery percentages. Although no evidences of statistically significant differences were observed between the expected and obtained concentrations, because of the susceptibility of the method to interference by other pesticides (e.g., parathion, dichlorvos) and natural organic matter (e.g., fulvic and humic acids), isolation of the analyte may be required when more complex sample matrices are encountered.

  18. Square-wave anodic-stripping voltammetric determination of Cd, Pb, and Cu in a hydrofluoric acid solution of siliceous spicules of marine sponges (from the Ligurian Sea, Italy, and the Ross Sea, Antarctica)

    Energy Technology Data Exchange (ETDEWEB)

    Truzzi, C.; Annibaldi, A.; Illuminati, S.; Bassotti, E.; Scarponi, G. [Polytechnic University of Marche, Ancona (Italy). Department of Marine Science

    2008-09-15

    Square-wave anodic-stripping voltammetry (SWASV) was set up and optimized for simultaneous determination of cadmium, lead, and copper in siliceous spicules of marine sponges, directly in the hydrofluoric acid solution ({proportional_to}0.55 mol L{sup -1} HF, pH {proportional_to}1.9). A thin mercury-film electrode (TMFE) plated on to an HF-resistant epoxy-impregnated graphite rotating-disc support was used. The optimum experimental conditions, evaluated also in terms of the signal-to-noise ratio, were as follows: deposition potential -1100 mV vs. Ag/AgCl, KCl 3 mol L{sup -1}, deposition time 3-10 min, electrode rotation 3000 rpm, SW scan from -1100 mV to +100 mV, SW pulse amplitude 25 mV, frequency 100 Hz, {delta}E{sub step} 8 mV, t{sub step} 100 ms, t{sub wait} 60 ms, t{sub delay} 2 ms, t{sub meas} 3 ms. Under these conditions the metal peak potentials were Cd -654{+-}1 mV, Pb -458 {+-} 1 mV, Cu -198{+-}1 mV. The electrochemical behaviour was reversible for Pb, quasi-reversible for Cd, and kinetically controlled (possibly following chemical reaction) for Cu. The linearity of the response with concentration was verified up to {proportional_to}4 {mu}g L{sup -1} for Cd and Pb and {proportional_to}20 {mu}g L{sup -1} for Cu. The detection limits were 5.8 ng L{sup -1}, 3.6 ng L{sup -1}, and 4.3 ng L{sup -1} for Cd, Pb, and Cu, respectively, with t{sub d}=5 min. The method was applied for determination of the metals in spicules of two specimens of marine sponges (Demosponges) from the Portofino natural reserve (Ligurian Sea, Italy, Petrosia ficiformis) and Terra Nova Bay (Ross Sea, Antarctica, Sphaerotylus antarcticus). The metal contents varied from tens of ng g{sup -1} to {proportional_to}1 {mu}g g{sup -1}, depending on the metal considered and with significant differences between the two sponge species. (orig.)

  19. Adsorption

    Directory of Open Access Journals (Sweden)

    Sushmita Banerjee

    2017-05-01

    Full Text Available Application of saw dust for the removal of an anionic dye, tartrazine, from aqueous solutions has been investigated. The experiments were carried out in batch mode. Effect of the parameters such as pH, initial dye concentration and temperature on the removal of the dye was studied. Equilibrium was achieved in 70 min. Maximum adsorption of dye was achieved at pH 3. Removal percent was found to be dependent on the initial concentration of dye solution, and maximum removal was found to be 97% at 1 mg/L of tartrazine. The removal increases from 71% to 97% when the initial concentration of dye solution decreases from 15 mg/L to 1 mg/L. The equilibrium adsorption data were analyzed by Langmuir, Freundlich, Temkin and Dubinin–Radushkevich isotherm models. The (Langmuir adsorption capacity of the adsorbent is found to be 4.71 mg/g at 318 K. Kinetic modeling of the process of removal was carried out and the process of removal was found to follow a pseudo second order model and the value of rate constant for adsorption process was calculated as 2.7 × 10−3 g mg−1 min−1 at 318 K. The thermodynamic parameters such as change in free energy (ΔG°, enthalpy (ΔH° and entropy (ΔS° were determined and the negative values of ΔG° indicated that the process of removal was spontaneous at all values of temperatures. Further, the values of ΔH° indicated the endothermic nature of the process of removal.

  20. VOLTAMMETRIC DETERMINATION OF CHLORAMPHENICOL AT ...

    African Journals Online (AJOL)

    a

    A sensitive square wave voltammetric method for the determination of ... involve UV-spectroscopy and HPLC, but have limited selectivity and ore often subjected to ..... The effect of the preservative associated with CAP in its pure form and its ...

  1. Optimization Central Composite Design for The Simultaneous Determination of Cd(II Ions in Fruit and Vegetable Samples by Adsorptive Stripping Voltammetry

    Directory of Open Access Journals (Sweden)

    Deswati

    2016-06-01

    Full Text Available This work describes a procedure for the simultaneous determination of cadmium in fruit and vegetable samples using adsorptive stripping voltammetry of complexes with calcon at a hanging mercury drop electrode (HMDE has been optimized using central composite design (CCD. The selection of the experimental conditions was made using experimental of the influence of several parameters were studied : variations of calcon concentration, pH, accumulation potential and accumulation time. The design experiment was a central composite design with 4 factors/variables, 3 levels and 31 treatment combinations. From analysis of variance, it was decided to accept the second-order model and the independent variable, concluded that a significant effect on the response variable (peak current. Based on data analysis with central composite design, the determination of cadmium obtained optimum conditions were : calcon concentration 0.8435 mM, pH 8.0047, accumulation potential -0.6346 Volt and accumulation time 81.85 seconds with a maximum peak current 61.8146 nA. At the optimum condition were obtained relative standard deviation 0.84%, recovery 98.88%, the linear range up to 110 µg/L, limit of detection 1.009 µg/L and LOQ 3.363 µg/L. The procedure was successfully applied to the determination of cadmium in fruit and vegetable samples without prior treatment.

  2. Differential pulse anodic stripping voltammetry for detection of As (III) by Chitosan-Fe(OH)3 modified glassy carbon electrode: A new approach towards speciation of arsenic.

    Science.gov (United States)

    Saha, Suparna; Sarkar, Priyabrata

    2016-09-01

    An efficient electrochemical sensor for As(III) was developed based on adsorption of arsenic on a specially modified electrodes at some applied potential and subsequent i) stripping at a fixed potential by anodic stripping voltammetry ii) analysis by generating surface plasmon resonance (SPR). The working glassy carbon electrode was modified by Chitosan-Fe(OH)3 composite and a reducing agent L-cysteine. The composite enhanced adsorption of As(III) and subsequent reduction to As(O) moieties and measurement by anodic stripping. The surface property of modified electrode was characterized by SEM, AFM, FTIR, XPS and electrochemistry was analyzed by impedance spectroscopy (EIS). Surface Plasmon resonance (SPR) was also employed to investigate the As(III) binding capability of polymer matrix. Several optimum voltammetric parameters e.g supporting electrolyte; 0.1M acetate buffer (pH 5.2) deposition potential, -0.9V; deposition time, 100s were established for anodic stripping voltammetry (ASV). A linear correlation was obtained in the range of 2-100ppb for ASV (R(2) 0.974) with limit of detection 0.072ppb. A variety of common coexistent ions such as Mn, Zn, Pb, Cu, Cd in water samples showed no interferences on the As (III) determination. The method was applied successfully to real samples collected from arsenic affected areas of West Bengal, India.

  3. Modified solid electrodes for stripping voltammetric determination of tin

    Energy Technology Data Exchange (ETDEWEB)

    Faller, C. [Kaiserslautern Univ. (Germany). Fachbereich Chemie]|[Univ. Trier (Germany). Abt. Anorganische und Analytische Chemie; Henze, G. [Kaiserslautern Univ. (Germany). Fachbereich Chemie]|[Univ. Trier (Germany). Abt. Anorganische und Analytische Chemie; Stojko, N. [Ural State Economic University, 8th of March Street 62, 620219 Ekaterinburg (Russian Federation); Saraeva, S. [Ural State Economic University, 8th of March Street 62, 620219 Ekaterinburg (Russian Federation); Brainina, K. [Ural State Economic University, 8th of March Street 62, 620219 Ekaterinburg (Russian Federation)

    1997-07-01

    The paper describes the determination of tin by ASV using modified thick film electrodes. Three different types of electrodes were developed: One modified with a mixture of Nafion and mercury(II)acetate, one modified with diethyldithiocarbamate (DDC) or pyrrolidinedithiocarbamate (PDC) and mercury(II)acetate, and one modified with calomel. The analyte was accumulated on the electrode surface after special electrochemical pretreatment of the modified electrode. After recording the voltammogram the electrodes were electrochemically regenerated. By virtue of their lifetime and their measurement reproducibility, we preferred the DDC and PDC modified electrodes. They can be used for months without changing their chemical characteristics. The linear range for tin determination with these electrodes is between 1 and 100 {mu}g/L; the detection limit was calculated as 0.9 {mu}g/L. The electrodes were applied to the direct determination of tin in different canned fruit juices without special sample pretreatment. (orig.). With 10 figs., 4 tabs.

  4. Electrochemical reduction and cathodic stripping voltammetric determination of clotrimazole

    OpenAIRE

    Pereira, Francisco C.; Stradiotto,Nelson R.; Zanoni,Maria Valnice B.

    2001-01-01

    Clotrimazol é reduzido em eletrodo de mercúrio em tampão fosfato pH > 6 através de um processo reversível de um elétron. O processo eletródico apresenta forte efeito de adsorção, o qual pode ser minimizado na presença de Triton X-100. Clotrimazol pode ser determinado em níveis de 50 ng mL-1 quando pré-acumulado durante 3 min à -0,20 V. O método proposto foi aplicado para determinação do fármaco em formulação comercial. The reduction of clotrimazole at a mercury electrode, in phosphate buff...

  5. Simultaneous determination of cefotaxime and desacetylcefotaxime in real urine sample using voltammetric and high-performance liquid chromatographic methods.

    Science.gov (United States)

    Aleksić, Mara M; Kapetanović, Vera; Atanacković, Jasmina; Jocić, Biljana; Zecević, Mira

    2008-10-19

    Two rapid, accurate and sensitive methods are developed and validated for the quantitative simultaneous determination of cefotaxime (CFX) and its active metabolite desacetylcefotaxime (DCFX) in urine. Based on the previous results which showed the four electron reduction of CFX at approximately -0.5 V, and the new findings that DCFX reduction occurred at more positive potential (-0.23 V), the new adsorptive stripping differential pulse voltammetric (AdSDPV) method was developed for determination of CFX in the presence of DCFX. Linear responses were observed over a wide concentration range (0.07-0.52 microg/ml for CFX and 0.22-1.3 microg/ml for DCFX) in urine. The second assay involves subsequent separation on a reversed-phase HPLC column, with ultraviolet detection at 262 nm. Retention times were 4.057 and 1.960 min for CFX and DCFX, respectively. Linear responses were observed over a wide range, 0.55-6.60 microg/ml for CFX and 1.10-11.00 microg/ml for DCFX, in urine. The statistical evaluation for both methods was examined by means of within-day repeatability (n=5) and day-to-day precision (n=3) and was found to be satisfactory with high accuracy and precision.

  6. Development of a voltammetric procedure for assay of the antihistamine drug hydroxyzine at a glassy carbon electrode: Quantification and pharmacokinetic studies.

    Science.gov (United States)

    Beltagi, A M; Abdallah, O M; Ghoneim, M M

    2008-01-15

    An electrochemical study of hydroxyzine at a glassy carbon electrode was carried out in the Britton-Robinson universal buffer of pH 2-11. Hydroxyzine was oxidized in a single two-electron irreversible process controlled mainly by adsorption. A simple, sensitive and time-saving square-wave adsorptive anodic stripping voltammetric procedure has been developed for determination of hydroxyzine in its commercial tablets and human serum without prior extraction. The optimized procedural conditions were: frequency=120Hz, scan increment=10mV, pulse-amplitude=25mV, accumulation potential=-0.3V, accumulation time=90-300s and a Britton-Robinson universal buffer of pH 4 as a supporting electrolyte. Mean recoveries of 100.5+/-0.71 and 98.6+/-1.12% (n=5) were achieved for assay of hydroxyzine in Atarax 10 and 25mg dosage forms, respectively. Limit of detection of 1.5x10(-8)molL(-1) (5.624ngmL(-1)) and limit of quantitation of 5.0x10(-8)molL(-1) (18.746ngmL(-1)) were achieved in human serum with a mean recovery of 98.4+/-1.22%, without prior extraction of the drug. Moreover, the described procedure was applied for evaluating the pharmacokinetic parameters of hydroxyzine in plasma of two healthy volunteers after administration of a single oral dose (Atarax)-25mg).

  7. New approach to the determination of contaminants of emerging concern in natural water: study of alprazolam employing adsorptive cathodic stripping voltammetry.

    Science.gov (United States)

    Nunes, Chalder Nogueira; Pauluk, Lucas Ely; Dos Anjos, Vanessa Egéa; Lopes, Mauro Chierici; Quináia, Sueli Pércio

    2015-08-01

    Contaminants of emerging concern (CECs) are chemicals, including pharmaceutical and personal care products, not commonly monitored in the aquatic environment. Pharmaceuticals are nowadays considered as an important environmental contaminant. Chromatography methods which require expensive equipment and complicated sample pretreatment are used for detection of CECs in natural water. Thus, in this study we proposed a simple, fast, and low-cost voltammetric method as a screening tool for the determination of CECs in natural water prior to chromatography. A case study was conducted with alprazolam (benzodiazepine). The method was optimized and validated in-house. The limit of quantification was 0.4 μg L(-1) for a 120 s preconcentration time. The recoveries ranged from 93 to 120 % for accuracy tests. A further proposal aim was to determine for the first time the occurrence of alprazolam in Brazilian river water and to evaluate its potential use as a marker of contamination by wastewater.

  8. Thrombin-Binding Aptamer Quadruplex Formation: AFM and Voltammetric Characterization

    Directory of Open Access Journals (Sweden)

    Victor Constantin Diculescu

    2010-01-01

    Full Text Available The adsorption and the redox behaviour of thrombin-binding aptamer (TBA and extended TBA (eTBA were studied using atomic force microscopy and voltammetry at highly oriented pyrolytic graphite and glassy carbon. The different adsorption patterns and degree of surface coverage were correlated with the sequence base composition, presence/absence of K+, and voltammetric behaviour of TBA and eTBA. In the presence of K+, only a few single-stranded sequences present adsorption, while the majority of the molecules forms stable and rigid quadruplexes with no adsorption. Both TBA and eTBA are oxidized and the only anodic peak corresponds to guanine oxidation. Upon addition of K+ ions, TBA and eTBA fold into a quadruplex, causing the decrease of guanine oxidation peak and occurrence of a new peak at a higher potential due to the oxidation of G-quartets. The higher oxidation potential of G-quartets is due to the greater difficulty of electron transfer from the inside of the quadruplex to the electrode surface than electron transfer from the more flexible single strands.

  9. Determination of Trace Amounts of Gold in Environmental Samples by Adsorptive Stripping Voltammetry of Its Complex with Rhodamine Using Osc-Pls

    Directory of Open Access Journals (Sweden)

    A. Akrami

    2012-11-01

    Full Text Available The multivariate calibration method was applied for the determination of trace amounts of gold based on a hanging mercury drop electrode (HMDE in the presence of rhodanine, followed by reduction of adsorbed gold by voltammetric scan using differential pulse modulation The optimum experimental conditions are: rhodanine concentration of 0.20 mg mL-1, pH 5.0, accumulation potential of -600 mV versus Ag/AgCl, accumulation time of 100 sec, scan rate of 30 mV s-1 and pulse height of 100 mV. The calibration matrix for partial least squares (PLS regression was designed with 9 samples. Orthogonal signal correction (OSC is a preprocessing technique used for removing the information unrelated to the target variables based on constrained principal component analysis. OSC is a suitable preprocessing method for PLS calibration without loss of prediction capacity using electrochemical method. The RMSEP for gold determination with PLS and OSC-PLS were 8.51 and 1.94, respectively. This procedure allows the determination of gold in synthetic and real samples with good reliability of the determination. 

  10. Simultaneous determination of Mn(II), Cu(II) and Fe(III) as 2-(5'-bromo-2'-pyridylazo)-5-diethylaminophenol complexes by adsorptive cathodic stripping voltammetry at a carbon paste electrode.

    Science.gov (United States)

    Ghoneim, Enass M

    2010-07-15

    A simple and precise square-wave adsorptive cathodic stripping voltammetry (SW-AdCSV) method has been described for simultaneous determination of Mn(II), Cu(II) and Fe(III) in water samples using a carbon paste electrode. In 0.1 mol L(-1) acetate buffer (pH 5) containing 50 micromol L(-1) of 2-(5'-bromo-2'-pyridylazo)-5-diethylaminophenol (5-Br-PADAP), Mn(II), Cu(II) and Fe(III) were simultaneously determined as metal-complexes with 5-Br-PADAP following preconcentration onto the carbon paste electrode by adsorptive accumulation at +1.0V (vs. Ag/AgCl/3M KCl). Insignificant interference from various cations (K(+), Na(+), Mg(2+), Ca(2+), Al(3+), Bi(3+), Sb(3+), Se(4+), Zn(2+), Ni(2+), Co(2+), Cd(2+), Pb(2+), V(5+), Ti(4+) and NH(4)(+)), anions (HCO(3)(-), Cl(-), NO(3-), SO(4)(2-) and PO(4)(3-)) and ascorbic acid was noticed. Limits of detection of 0.066, 0.108 and 0.093 microg L(-1) and limits of quantitation of 0.22, 0.36 and 0.31 microg L(-1) Mn(II), Cu(II) and Fe(III), respectively, were achieved by the described method. The described stripping voltammetry method was successfully applied for simultaneous determination of Mn(II), Cu(II) and Fe(III) in ground, tap and bottled natural water samples. Copyright 2010 Elsevier B.V. All rights reserved.

  11. Square-Wave Voltammetric Determination of Sulpiride

    OpenAIRE

    1999-01-01

    The basic redox properties of sulpiride are investigated by means of cyclic voltammetry and square-wave voltammetryat a hanging mercury drop electrode. Sulpiride undergoes electrochemical reaction in basic media. The voltammetric response of sulpiride strongly depends on pH of the medium. A square-wave method for quantitative determination of sukpiride was developed.

  12. Ion-transfer voltammetric determination of folic acid at meso-liquid-liquid interface arrays.

    Science.gov (United States)

    Jiang, Xuheng; Gao, Kui; Hu, Daopan; Wang, Huanhuan; Bian, Shujuan; Chen, Yong

    2015-04-21

    Voltammetric studies on the simple ion transfer (IT) behaviors of an important water-soluble B-vitamin, folic acid (FA), at the liquid-liquid (L-L) interface were firstly performed and then applied as a novel detection method for FA under physiological conditions. Meso-water-1,6-dichlorohexane (W-DCH) and meso-water-organogel interface arrays were built by using a hybrid mesoporous silica membrane (HMSM) with a unique structure of pores-in-pores and employed as the new platforms for the IT voltammetric study. In view of the unique structure of the HMSM, the impact of the ionic surfactant cetyltrimethylammonium bromide (CTAB), self-assembled within the silica nanochannels of the HMSM, was investigated. In particular, its effect on the IT voltammetric behavior and detection of FA at meso-L-L interface arrays was systematically examined by cyclic voltammetry (CV), differential pulse voltammetry (DPV) and differential pulse stripping voltammetry (DPSV). It was found that all the voltammetric responses of CV, DPV, and DPSV and the corresponding detection limit of FA at such meso-L-L interface arrays are closely related to the CTAB in the HMSM. Significantly, the calculated detection limit of FA could be improved to 80 nM after the combination of the DPSV technique with the additional preconcentration of FA in the silica-CTAB nanochannels, achieved through an anion-exchange process between FA(-) and the bromide of CTAB in HMSM. This provides a new and attractive strategy for the detection of those biological anions.

  13. Determination of aluminium in water samples by adsorptive cathodic stripping voltammetry in the presence of pyrogallol red and a quaternary ammonium salt.

    Science.gov (United States)

    Arancibia, Verónica; Muñoz, Carolina

    2007-09-30

    A fast, sensitive and selective method for the determination of aluminium based on the reaction of the metal with pyrogallol red (PR) in the presence of tetrabutylammonium tetrafluoroborate (TBATFB) to form an Al(PR)(3)x9TBATFB complex which is adsorbed on the mercury electrode is presented. Under these conditions complexation of aluminium is rapid and no waiting period or heating of the sample is required. The reduction current of the accumulated complex is measured by scanning the potential in the cathodic direction. The variation of peak current with pH, adsorption time, adsorption potential, ligand and quaternary ammonium salt concentration, and some instrumental parameters, such as stirring rate in the accumulation stage, and step amplitude, pulse amplitude and step duration while obtaining the square wave voltamperograms were optimized. The best experimental parameters were pH 8.5, (NH(4)Ac-NH(3) buffer), C(PR)=25mumolL(-1), C(TBATFB) over 75mumolL(-1), t(ads)=60s, and E(ads)=-0.60V versus Ag/AgCl. A linear response is observed over the 0.0-30.0mugL(-1) concentration range, with a detection limit of 1.0mugL(-1). Reproducibility for 9.0mugL(-1) aluminium solution was 2.3% (n=6). Synthetic sea water and sea water reference material CRM-SW were used for validation measurements. Aluminium in urine samples of a volunteer who ingested 800mg of Al(OH)(3) was analyzed.

  14. Voltammetric behaviour and determination of clonazepam using a disposable screen-printed sensor and its determination in serum and wine

    OpenAIRE

    Honeychurch, K. C.; Brooks, J.; Hart, J. P.

    2016-01-01

    Clonazepam\\ud Screen-printed Carbon Electrodes\\ud Cyclic Voltammetry\\ud Gas chromatography mass spectrometry\\ud Adsorptive Stripping Voltammetry\\ud Sample Preparation and Analysis\\ud Conclusions

  15. Voltammetric behaviour and determination of clonazepam using a disposable screen-printed sensor and its determination in serum and wine

    OpenAIRE

    Honeychurch, K. C.; Brooks, J.; Hart, J. P.

    2016-01-01

    Clonazepam\\ud Screen-printed Carbon Electrodes\\ud Cyclic Voltammetry\\ud Gas chromatography mass spectrometry\\ud Adsorptive Stripping Voltammetry\\ud Sample Preparation and Analysis\\ud Conclusions

  16. Voltammetric Investigation Of Hydrothermal Iron Speciation

    Directory of Open Access Journals (Sweden)

    Charlotte eKleint

    2016-05-01

    Full Text Available Hydrothermal vent fluids are highly enriched in iron (Fe compared to ambient seawater, and organic ligands may play a role in facilitating the transport of some hydrothermal Fe into the open ocean. This is important since Fe is a limiting micronutrient for primary production in large parts of the world`s surface ocean. We have investigated the concentration and speciation of Fe in several vent fluid and plume samples from the Nifonea vent field, Coriolis Troughs, New Hebrides Island Arc, South Pacific Ocean using competitive ligand exchange - adsorptive cathodic stripping voltammetry (CLE - AdCSV with salicylaldoxime (SA as the artificial ligand. Our results for total dissolved Fe (dFe in the buoyant hydrothermal plume samples showed concentrations up to 3.86 µM dFe with only a small fraction between 1.1% and 11.8% being chemically labile. Iron binding ligand concentrations ([L] were found in µM level with strong conditional stability constants up to log K[L],Fe3+ of 22.9. Within the non-buoyant hydrothermal plume above the Nifonea vent field, up to 84.7% of the available Fe is chemically labile and [L] concentrations up to 97 nM were measured. [L] was consistently in excess of Felab, indicating that all available Fe is being complexed, which in combination with high Felab values in the non-buoyant plume, signifies that a high fraction of hydrothermal dFe is potentially being transported away from the plume into the surrounding waters, contributing to the global oceanic Fe budget.

  17. Voltammetric Detection of Diquat at the Carbon Paste Electrode Containing a Ca10(PO46(OH2

    Directory of Open Access Journals (Sweden)

    Moulay Abderrahim EL MHAMMEDI

    2007-01-01

    Full Text Available We report a sensitive electrochemical voltammetric method for analyzing diquat (DQ ions using a carbon paste electrochemical (CPE modified by porous material, such as hydroxyapatite (HAP. Diquat strongly adsorbed on a HAP-CPE surface and provides facile electrochemical quantitative methods for electroactive DQ ions. Operational parameters have been optimized, and the stripping voltammetric performance has been studied using square wave voltammetry. The peaks current intensity are highly linear over the 7×10-7–3×10-4 mol L-1 diquat range examined (10-min accumulation time, with a good sensitivity. These findings can lead to a widespread use of electrochemical sensors to detect DQ contaminates.Scanning electron microscopy was used for morphology observation and in particular the X-ray diffraction analysis (XRD and Fourier transformed infrared spectroscopy (FTIR analysis for characterization of synthesis powder.

  18. A solid paraffin-based carbon paste electrode modified with 2-aminothiazole organofunctionalized silica for differential pulse adsorptive stripping analysis of nickel in ethanol fuel

    Energy Technology Data Exchange (ETDEWEB)

    Takeuchi, Regina M. [Departamento de Quimica Analitica, Instituto de Quimica, UNESP, CP 355, 14801-970 Araraquara, SP (Brazil)]. E-mail: takeuchi@iq.unesp.br; Santos, Andre L. [Departamento de Quimica Analitica, Instituto de Quimica, UNESP, CP 355, 14801-970 Araraquara, SP (Brazil); Padilha, Pedro M. [Departamento de Quimica e Bioquimica-IB/UNESP, CP 510, 18618-000 Botucatu, SP (Brazil); Stradiotto, Nelson R. [Departamento de Quimica Analitica, Instituto de Quimica, UNESP, CP 355, 14801-970 Araraquara, SP (Brazil)

    2007-02-19

    A solid paraffin-based carbon paste electrode modified with 2-aminothiazole organofunctionalized silica (SiAt-SPCPE) was applied to Ni{sup 2+} determination in commercial ethanol fuel samples. The proposed method comprised four steps: (1) Ni{sup 2+} preconcentration at open circuit potential directly in the ethanol fuel sample, (2) transference of the electrode to an electrochemical cell containing DMG, (3) differential pulse voltammogram registering and (4) surface regeneration by polishing the electrode. The proposed method combines the high Ni{sup 2+} adsorption capacity presented by 2-aminothiazole organofunctionalized silica with the electrochemical properties of the Ni(DMG){sub 2} complex, whose electrochemical reduction provides the analytical signal. All experimental parameters involved in the proposed method were optimized. Using a preconcentration time of 20 min, it was obtained a linear range from 7.5 x 10{sup -9} to 1.0 x 10{sup -6} mol L{sup -1} with detection limit of 2.0 x 10{sup -9} mol L{sup -1}. Recovery values between 96.5 and 102.4% were obtained for commercial samples spiked with 1.0 {mu}mol L{sup -1} Ni{sup 2+} and the developed electrode was totally stable in ethanolic solutions. The contents of Ni{sup 2+} found in the commercial samples using the proposed method were compared to those obtained by graphite furnace atomic absorption spectroscopy by using the F- and t-test. Neither the F- nor t-values exceeded the critical values at 95% confidence level, confirming that there are not statistical differences between the results obtained by both methods. These results indicate that the developed electrode can be successfully employed to reliable Ni{sup 2+} determination in commercial ethanol fuel samples without any sample pretreatment or dilution step.

  19. Quantification of iron in seawater at the low picomolar range based on optimization of bromate/ammonia/dihydroxynaphtalene system by catalytic adsorptive cathodic stripping voltammetry.

    Science.gov (United States)

    Laglera, Luis Miguel; Santos-Echeandía, Juan; Caprara, Salvatore; Monticelli, Damiano

    2013-02-19

    A new analytical protocol for the challenging analysis of total dissolved iron at the low picomolar level in oceanic waters suitable for onboard analysis is presented. The method is based on the revision of the adsorptive properties of the iron/2,3-dihydroxynaphthalene (Fe/DHN) complexes on the hanging mercury drop electrode with catalytic enhancement by bromate ions. Although it was based on a previously proposed reagent combination, we show here that the addition of an acidification/alkalinization step is essential in order to cancel any organic complexation, and that an extra increment of the pH to 8.6-8.8 leads to the definition of a preconcentration-free procedure with the lowest detection limit described up to now. For total dissolved iron analysis, samples were acidified to pH 2.0 in the presence of 30 μM DHN and left to equilibrate overnight. A 10 mL sample was subsequently buffered to a pH of ∼8.7 in the presence of 20 mM bromate: a 60 s deposition at 0 V led to a sensitivity of 34 nA nM(-1) min(-1), a 4-fold improvement over previous methods, that translated in a limit of detection of 5 pM (2-20 fold improvement). Several tests proved that a nonreversible reaction in the time scale of the analysis, triggered by the acidification/alkalinization step, was behind the signal magnification. The new method was validated onboard via the analysis of reference material and via intercalibration against flow injection analysis-chemiluminescence on Southern Ocean surface samples.

  20. Increased sensitivity of anodic stripping voltammetry at the hanging mercury drop electrode by ultracathodic deposition.

    Science.gov (United States)

    Rodrigues, José A; Rodrigues, Carlos M; Almeida, Paulo J; Valente, Inês M; Gonçalves, Luís M; Compton, Richard G; Barros, Aquiles A

    2011-09-09

    An improved approach to the anodic stripping voltammetric (ASV) determination of heavy metals, using the hanging mercury drop electrode (HMDE), is reported. It was discovered that using very cathodic accumulation potentials, at which the solvent reduction occurs (overpotential deposition), the voltammetric signals of zinc(II), cadmium(II), lead(II) and copper(II) increase. When compared with the classical methodology a 5 to 10-fold signal increase is obtained. This effect is likely due to both mercury drop oscillation at such cathodic potentials and added local convection at the mercury drop surface caused by the evolution of hydrogen bubbles. Copyright © 2011 Elsevier B.V. All rights reserved.

  1. General theory of cathodic and anodic stripping voltammetry at solid electrodes: mathematical modeling and numerical simulations.

    Science.gov (United States)

    Ward Jones, Sarah E; Chevallier, François G; Paddon, Christopher A; Compton, Richard G

    2007-06-01

    Theory is presented to describe the voltammetric signals associated with the stripping phase of stripping voltammetry at solid electrodes. Three mathematical models are considered, and the importance of the hemispherical diffusion associated with electrochemical dissolution of particles in the micrometer range is investigated. Model A considers a "monolayer" system where the coverage at a specific point cannot exceed a maximum value. Model B considers a thin layer of metal or metal oxide, but in contrast to model A, the maximum surface coverage is not restricted. Model C represents the stripping of a "thick layer" where the deposition is also unrestricted.

  2. Sensitive voltammetric determination of lead released from ceramic dishes by using of bismuth nanostructures anchored on biochar.

    Science.gov (United States)

    Agustini, Deonir; Mangrich, Antonio Salvio; Bergamini, Márcio F; Marcolino-Junior, Luiz Humberto

    2015-09-01

    A simple and sensitive electroanalytical method was developed for determination of nanomolar levels of Pb(II) based on the voltammetric stripping response at a carbon paste electrode modified with biochar (a special charcoal) and bismuth nanostructures (nBi-BchCPE). The proposed methodology was based on spontaneous interactions between the highly functionalized biochar surface and Pb(II) ions followed by reduction of these ions into bismuth nanodots which promote an improvement on the stripping anodic current. The experimental procedure could be summarized in three steps: including an open circuit pre-concentration, reduction of accumulated lead ions at the electrode surface and stripping step under differential pulse voltammetric conditions (DPAdSV). SEM images revealed dimensions of bismuth nanodots ranging from 20 nm to 70 nm. The effects of main parameters related to biochar, bismuth and operational parameters were examined in detail. Under the optimal conditions, the proposed sensor has exhibited linear range from 5.0 to 1000 nmol L(-1) and detection limit of 1.41 nmol L(-1) for Pb(II). The optimized method was successfully applied for determination of Pb(II) released from overglaze-decorated ceramic dishes. Results obtained were compared with those given by inductively coupled plasma optical emission spectroscopy (ICP-OES) and they are in agreement at 99% of confidence level. Copyright © 2015. Published by Elsevier B.V.

  3. Penicillamine-modified sensor for the voltammetric determination of Cd(II) and Pb(II) ions in natural samples.

    Science.gov (United States)

    Pérez-Ràfols, Clara; Serrano, Núria; Díaz-Cruz, José Manuel; Ariño, Cristina; Esteban, Miquel

    2015-11-01

    A new penicillamine-GCE was developed based on the immobilization of d-penicillamine on aryl diazonium salt monolayers anchored to the glassy carbon electrode (GCE) surface and it was applied for the first time to the simultaneous determination of Cd(II) and Pb(II) ions by stripping voltammetric techniques. The detection and quantification limits at levels of µg L(-1) suggest that the penicillamine-GCE could be fully suitable for the determination of the considered ions in natural samples.

  4. Microconcentric ring electrode/injector assembly for sensitive voltammetric analysis in single droplets of ultrasmall volumes.

    Science.gov (United States)

    Kai, Tianhan; Chen, Shu; Monterroso, Estuardo; Hailu, Amanuel; Zhou, Feimeng

    2014-08-19

    This paper describes the construction of a microring electrode concentric to an inner injection capillary for voltammetric determination of trace analytes in nanoliter- to picoliter-sized droplets. The gold microring is sandwiched between a pulled fused-silica capillary and borosilicate glass tubing. Compared to polymer-coated microring electrodes, the glass-encapsulated electrode is more robust and does not swell in organic solvents. Consequently, the microring electrode is suitable for voltammetric studies of redox-active species and their accompanying ion transfers between two immiscible solvents. Droplets of variable sizes can be conveniently dispensed from front-loaded sample plugs into an immiscible liquid, greatly simplifying the experimental procedure and facilitating analysis of samples of limited availability. The size of the microring and the volume of the droplet deduced from well-defined voltammograms correlate well with those estimated from their geometric dimensions. The thin-layer cell behavior can be attained with well-defined voltammetric peaks and small capacitive current. Exhaustive electrolysis in single droplets can be accomplished in short times (e.g., ∼85 s in a droplet of 1.42 nL at a microring of 11.4 μm in radius). Anodic stripping voltammetry of Ag deposited onto the microring electrode resulted in a detection limit of 0.13 fmol (14 fg) of Ag(+). The microring electrode/injector assembly can be polished repeatedly and is versatile for various applications (e.g., sample plugs can also be back-loaded via a rotary injection valve and an HPLC pump for flow injection analysis).

  5. Voltammetric determination of imidacloprid and thiamethoxam

    Directory of Open Access Journals (Sweden)

    SZILVIA N. ÖKRÉSZ

    2005-05-01

    Full Text Available A simple voltammetric method using a glassy carbon working electrode was developed for the determination of two members from the neonicotinoid group of insecticides: imidacloprid and thiamethoxam. The experiments showed that the voltammetric response depends on the mode of electrode surface pretreatment and the polarization mode. The response appeared to be linear in the range from 0.028 to 0.50 mg/cm3 for both analytes. The limit of detection was 0.0077 mg/cm3 for imidacloprid and 0.0085 mg/cm3 for thiamethoxam, the limit of quantitation was 0.026 mg/cm3 and 0.028 mg/cm3, respectively. The developed method was applied for the determination of these insecticides in potato samples sprayed with Confidor 200-SL or Actara 25-WG as well as commercial formulations of imidacloprid and thiamethoxam. Arecovery trial was performed to assess the accuracy of the results, the recovery values being between 95–102 % for both of neonicotinoids.

  6. TRACE LEVEL VOLTAMMETRIC DETERMINATION OF HEAVY METALS AND TOTAL MERCURY IN TEA MATRICES (Camellia sinensis).

    Science.gov (United States)

    Melucci, Dora; Locatelli, Marcello; Locatelli, Clinio

    2013-10-24

    An analytical procedure regarding the voltammetric determination of mercury(II), copper(II), lead(II), cadmium(II) and zinc(II) by square wave anodic stripping voltammetry (SWASV) in matrices involved in food chain is proposed. In particular, tea leaves were analysed as real samples. The digestion of each matrix was carried out using a concentrated HCl-HNO3-H2SO4 acidic attack mixture; 0.01 mol L(-1) EDTA-Na2 + 0.15 mol L(-1) NaCl + 0.5 mol L(-1) HCl was employed as the supporting electrolyte. The voltammetric measurements were carried out using a conventional three electrode cell, employing, as working electrodes, a gold electrode (GE) and a stationary hanging mercury drop electrode (HMDE). The analytical procedure has been verified on the standard reference materials Spinach Leaves NIST-SRM 1570a, Tomato Leaves NIST-SRM 1573a and Apple Leaves NIST-SRM 1515. For all the elements, the precision as repeatability, expressed as relative standard deviation (sr) was of the order of 3-5 %, while the trueness, expressed as relative error (e) was of the order of 3-7 %. Once set up on the standard reference materials, the analytical procedure was applied to commercial tea leaves samples. A critical comparison with spectroscopic measurements is also discussed.

  7. Evaluation of antimony microparticles supported on biochar for application in the voltammetric determination of paraquat.

    Science.gov (United States)

    Gevaerd, Ava; de Oliveira, Paulo R; Mangrich, Antonio S; Bergamini, Márcio F; Marcolino-Junior, Luiz H

    2016-05-01

    This work describes the construction and application of carbon paste electrodes modified with biochar and antimony microparticles (SbBCPE) for voltammetric determination of paraquat using a simple and sensitive procedure based on voltammetric stripping analysis. Some parameters such as amount of biochar and antimony used in the composition of the carbon paste and instrumental parameters were examined in detail. Under optimized conditions, an analytical curve was obtained for paraquat determination employing SbBCPE, which showed a linear response ranging from 0.2 to 2.9 μmol L(-1), with limit of detection and quantification of 34 nmol L(-1) and 113 nmol L(-1), respectively, after paraquat pre-concentration of 120 s. The repeatability study presented a RSD=2.0% for 10 consecutive measurements using the same electrode surface and the reproducibility study showed a RSD=2.7% for measurements with 10 different electrode surfaces. The proposed sensor was successfully applied for paraquat determination in tap water and citric fruit juice spiked samples and good recoveries were obtained without any sample pre-treatment, showing its promising analytical performance.

  8. Voltammetric copper(II) determination with a montmorillonite-modified carbon paste electrode

    Energy Technology Data Exchange (ETDEWEB)

    Kula, P. [Institute of Geonics, Academy of Sciences of Czech Republic, Studertska 1768, 708 00 Ostrava (Czech Republic); Navratilova, Z. [Institute of Geonics, Academy of Sciences of Czech Republic, Studertska 1768, 708 00 Ostrava (Czech Republic)

    1996-03-01

    The clay mineral montmorillonite has been tested as modifier for the carbon paste electrode with a novel electrode modification technique. The differential pulse voltammetric determination of copper(II) by means of this modified carbon paste electrode has been studied. A detection limit of 4 x 10{sup -8} mol/l has been achieved after 10 min preconcentration under open circuit conditions with subsequent anodic stripping voltammetry. The calibration curve for Cu(II) is linear in the range of 4 x 10{sup -8}-8 x 10{sup -7} mol/l. Pb interferes in a 10-fold molar and Cd and Hg in a 100-fold molar excess. The interference by humic ligands is significant. (orig.). With 5 figs., 1 tab.

  9. The Strip Module

    DEFF Research Database (Denmark)

    Pedersen, Tommy

    1996-01-01

    -ship code available at the department. It will be structured as a general preprocessor mainly to determine the hydrodynamic mass and damping. A strip processor including three different theories: A linear frequency domain strip theory, a quadratic strip theory and a nonlinear time domain strip theory...

  10. Voltammetric and theoretical studies of electrochemical behavior of cephalosporins at the mercury electrode

    Directory of Open Access Journals (Sweden)

    Nikolić Katarina

    2015-01-01

    Full Text Available Study of the adsorption and electroreduction behavior of cefpodoxime proxetil, cefotaxime, desacetylcefotaxime, cefetamet, ceftriaxone, ceftazidime, and cefuroxime axetile at the mercury electrode surface has been performed using Cyclic (CV, Differential Pulse (DPV, and Adsorptive Stripping Differential Pulse Voltammetry (AdSDPV. The Quantitative Structure Property Relationship (QSPR study of the seven cephalosporins adsorption at the mercury electrode has been based on the density functional theory DFT-B3LYP/6-31G (d,p calculations of molecular orbitals, partial charges and electron densities of analytes. The DFT-parameters and QSPR model explain well the process of adsorption of the examined cephalosporins. QSPR study defined that cefalosporins with lower charge of sulphur in the thiazine moiety, lower electron density on the nitrogen atom of the N-O bond, higher number of hydrogen bond accepting groups, and higher principal moment of inertia should express high adsorption on the mercury electrode. [Projekat Ministarstva nauke Republike Srbije, br. 172033

  11. Novel electrochemical biosensor based on PVP capped CoFe2O4@CdSe core-shell nanoparticles modified electrode for ultra-trace level determination of rifampicin by square wave adsorptive stripping voltammetry.

    Science.gov (United States)

    Asadpour-Zeynali, Karim; Mollarasouli, Fariba

    2017-06-15

    This work introduces a new electrochemical sensor based on polyvinyl pyrrolidone capped CoFe2O4@CdSe core-shell modified electrode for a rapid detection and highly sensitive determination of rifampicin (RIF) by square wave adsorptive stripping voltammetry. The new PVP capped CoFe2O4@CdSe with core-shell nanostructure was synthesized by a facile synthesis method for the first time. PVP can act as a capping and etching agent for protection of the outer surface nanoparticles and formation of a mesoporous shell, respectively. Another important feature of this work is the choice of the ligand (1,10-phenanthroline) for precursor cadmium complex that works as a chelating agent in order to increase optical and electrical properties and stability of prepared nanomaterial. The nanoparticles have been characterized by field emission scanning electron microscopy (FESEM), transmission electron microscope (TEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), UV-vis, photoluminescence (PL) spectroscopy, FT-IR, and cyclic voltammetry techniques. The PL spectroscopy study of CoFe2O4@CdSe has shown significant PL quenching by the formation of CoFe2O4 core inside CdSe, this shows that CoFe2O4 NPs are efficient electron acceptors with the CdSe. It is clearly observed that the biosensor can significantly enhance electrocatalytic activity towards the oxidation of RIF, under the optimal conditions. The novelty of this work arises from the new synthesis method for the core-shell of CoFe2O4@CdSe. Then, the novel electrochemical biosensor was fabricated for ultra-trace level determination of rifampicin with very low detection limit (4.55×10(-17)M) and a wide linear range from 1.0×10(-16) to 1.0×10(-7)M. The fabricated biosensor showed high sensitivity and selectivity, good reproducibility and stability. Therefore, it was successfully applied for the determination of ultra-trace RIF amounts in biological and pharmaceutical samples with satisfactory recovery data.

  12. Cyclic Voltammetric Responses of Nitrate Reductase on Chemical Modified Electrodes

    Institute of Scientific and Technical Information of China (English)

    YaRuSONG; HuiBoSHAO; 等

    2002-01-01

    Electrochemistry of nitrate reductases (NR) incorporated into 2-aminoethanethiol self-assembled on the gold electrode and polyacrylamide cast on the pyrolytic graphite electrode was examined. NR on chemical modified electrode showed electrochemical cyclic voltammetric responses in phosphate buffers.

  13. Voltammetric behaviour of oligonucleotide lipoplexes adsorbed onto glassy carbon electrodes

    OpenAIRE

    Piedade, J. A. P.; M. Mano; Lima, M. C. Pedroso de; Oretskaya, T S; Oliveira-Brett, A. M.

    2004-01-01

    The voltammetric behaviour of oligonucleotide lipoplexes (ODN-lipoplexes) prepared from short oligodeoxynucleotides (ODN), with different base compositions, and liposomes of the cationic lipid DOTAP, was studied by differential pulse voltammetry with a glassy carbon mini-electrode. It was found that the ODN base composition influences the ODN-lipoplex voltammetric response. Differential pulse voltammograms for ODN-lipoplexes of the ODN adenosine nucleotides present two different features when...

  14. Approximate strip exchanging.

    Science.gov (United States)

    Roy, Swapnoneel; Thakur, Ashok Kumar

    2008-01-01

    Genome rearrangements have been modelled by a variety of primitives such as reversals, transpositions, block moves and block interchanges. We consider such a genome rearrangement primitive Strip Exchanges. Given a permutation, the challenge is to sort it by using minimum number of strip exchanges. A strip exchanging move interchanges the positions of two chosen strips so that they merge with other strips. The strip exchange problem is to sort a permutation using minimum number of strip exchanges. We present here the first non-trivial 2-approximation algorithm to this problem. We also observe that sorting by strip-exchanges is fixed-parameter-tractable. Lastly we discuss the application of strip exchanges in a different area Optical Character Recognition (OCR) with an example.

  15. Cathodic stripping voltammetry of trace Mn(II) at carbon film electrodes

    OpenAIRE

    Filipe, Olga M. S.; Brett,Christopher M.A.

    2003-01-01

    A sensitive voltammetric method is presented for the determination of tract levels of Mn (II) using carbon film electrodes fabricated from carbon resistors of 2 [Omega]. Determination of manganese was made by square wave cathodic stripping voltammetry (CSV), with deposition of manganese as manganese dioxide. Chronoamperometric experiments were made to study MnO2 nucleation and growth. As a result, it was found to be necessary to perform electrode conditioning at a more positive potential to i...

  16. Voltammetric studies on the electrochemical determination of methylmercury in chloride medium at carbon microelectrodes

    Energy Technology Data Exchange (ETDEWEB)

    Ribeiro, F. [Centro de Electroquimica e Cinetica da Universidade de Lisboa, Departamento de Quimica e Bioquimica, Faculdade de Ciencias, Universidade de Lisboa, Campo Grande, Ed. C8, 1749-016 Lisbon (Portugal); Neto, M.M.M. [Centro de Electroquimica e Cinetica da Universidade de Lisboa, Departamento de Quimica e Bioquimica, Faculdade de Ciencias, Universidade de Lisboa, Campo Grande, Ed. C8, 1749-016 Lisbon (Portugal) and Departamento de Quimica Agricola e Ambiental, Instituto Superior de Agronomia, Tapada da Ajuda, 1349-017 Lisbon (Portugal)]. E-mail: mm.neto@netcabo.pt; Rocha, M.M. [Centro de Electroquimica e Cinetica da Universidade de Lisboa, Departamento de Quimica e Bioquimica, Faculdade de Ciencias, Universidade de Lisboa, Campo Grande, Ed. C8, 1749-016 Lisbon (Portugal); Fonseca, I.T.E. [Centro de Electroquimica e Cinetica da Universidade de Lisboa, Departamento de Quimica e Bioquimica, Faculdade de Ciencias, Universidade de Lisboa, Campo Grande, Ed. C8, 1749-016 Lisbon (Portugal)

    2006-10-10

    Electroanalytical techniques have been used to determine methylmercury at low levels in environmental matrices. The electrochemical behaviour of methylmercury at carbon microelectrodes in a hydrochloric acid medium using cyclic, square wave and fast-scan linear-sweep voltammetric techniques has been investigated. The analytical utility of the methylmercury reoxidation peak has been explored, but the recorded peak currents were found to be poorly reproducible. This is ascribed to two factors: the adsorption of insoluble chloromercury compounds on the electrode surface, which appears to be an important contribution to hinder the voltammetric signal of methylmercury; and the competition between the reoxidation of the methylmercury radical and its dimerization reaction, which limits the reproducibility of the methylmercury peak. These problems were successfully overcome by adopting the appropriate experimental conditions. Fast-scan rates were employed and an efficient electrochemical regeneration procedure of the electrode surface was achieved, under potentiostatic conditions in a mercury-free solution containing potassium thiocyanate-a strong complexing agent. The influence of chloride ion concentration was analysed. Interference by metals, such as lead and cadmium, was considered. Calibration plots were obtained in the micromolar and submicromolar concentration ranges, allowing the electrochemical determination of methylmercury in trace amounts. An estuarine water sample was analysed using the new method with a glassy carbon microelectrode.

  17. Voltammetric behaviour of drotaverine hydrochloride in surfactant media and its enhancement determination in Tween-20.

    Science.gov (United States)

    Jain, Rajeev; Vikas; Rather, Jahangir Ahmad

    2011-02-01

    Simple, sensitive and rapid adsorptive voltammetric behaviour of drotaverine hydrochloride onto the HMDE has been explored and validated in surfactant media by using cyclic, differential pulse and square-wave voltammetry. Addition of Tween-20 to the drotaverine hydrochloride containing electrolyte enhances the reduction current signal. The voltammograms of the drug with Tween-20 in phosphate buffers of pH 2.5-11.0 exhibit a single well defined reduction peak which may be due to the reduction of -CC- group. The cyclic voltammetric studies indicated the reduction of drotaverine hydrochloride at the electrode surface through two electron irreversible step and diffusion-controlled. The peak current showed a linear dependence with the drug concentration over the range 0.8-7.2μgmL(-1). The calculated LOD and LOQ are 1.8 and 6.0ngmL(-1) by SWCAdSV and 8.1 and 27.2ngmL(-1) by DPCAdSV, respectively. The procedure was applied to the assay of the drug in tablet form with mean percentage recoveries of 100.2% with SWCAdSV and 99.7% with DPCAdSV. The validity of the proposed methods was further assessed by applying a standard addition technique.

  18. The Strip Module

    DEFF Research Database (Denmark)

    Pedersen, Tommy

    1996-01-01

    When the behaviour of a ship in waves is to be predicted it is convenient to have a tool which includes different approaches to the problem.The aim of this project is to develop such a tool named the strip theory module. The strip theory module will consist of submodules dependent on the I......-ship code available at the department. It will be structured as a general preprocessor mainly to determine the hydrodynamic mass and damping. A strip processor including three different theories: A linear frequency domain strip theory, a quadratic strip theory and a nonlinear time domain strip theory...

  19. Square-wave stripping voltammetry for direct determination of eight heavy metals in soil and indoor-airborne particulate matter.

    Science.gov (United States)

    Farghaly, Othman A; Ghandour, M A

    2005-03-01

    The application of square-wave voltammetry (SWV) for the determination of eight elements viz. Cd(II), Pb(II), Cu(II), Zn(II), Co(II), Ni(II), Cr(VI), and Mo(VI) in soil and indoor-airborne particulate matter has been examined and optimized. The cathodic and anodic types of the SWV technique were examined for the detection of these metal ions. It was found that the square-wave anodic stripping voltammetry is the conventional technique for the determination of Zn(II), Cd(II), Pb(II), and Cu(II), but square-wave adsorptive cathodic stripping voltammetric method is used for the determination of Co(II), Ni(II), Mo(VI) and Cr(VI). Various experimental parameters, which influenced the response of the mercury film electrode to these metal ions, were optimized. The detection limits of these metal ions were 0.03, 0.4, 0.04, 0.1, 0.15, 0.05, 0.2, and 3.2 microg/kg for Cd(II), Pb(II), Cu(II), Zn(II), Co(II), Ni(II), Cr(VI), and Mo(VI), respectively, with very good accuracy (standard deviation is below 2%). Interference from coexisting ions was successfully investigated. A comparison of analytical data for analyzing real samples was carried out between the SWV method and the graphite furnace atomic absorption spectrophotometric (GFAAS) method. By the standard addition method, the recoveries were 96.6-104% with SD of 0.75-2.5%. The great advantage of SWV is the simplicity, selectivity, sensitivity, and shortening analysis time over the GFAAS method.

  20. Active voltammetric microsensors with neural signal processing.

    Energy Technology Data Exchange (ETDEWEB)

    Vogt, M. C.

    1998-12-11

    Many industrial and environmental processes, including bioremediation, would benefit from the feedback and control information provided by a local multi-analyte chemical sensor. For most processes, such a sensor would need to be rugged enough to be placed in situ for long-term remote monitoring, and inexpensive enough to be fielded in useful numbers. The multi-analyte capability is difficult to obtain from common passive sensors, but can be provided by an active device that produces a spectrum-type response. Such new active gas microsensor technology has been developed at Argonne National Laboratory. The technology couples an electrocatalytic ceramic-metallic (cermet) microsensor with a voltammetric measurement technique and advanced neural signal processing. It has been demonstrated to be flexible, rugged, and very economical to produce and deploy. Both narrow interest detectors and wide spectrum instruments have been developed around this technology. Much of this technology's strength lies in the active measurement technique employed. The technique involves applying voltammetry to a miniature electrocatalytic cell to produce unique chemical ''signatures'' from the analytes. These signatures are processed with neural pattern recognition algorithms to identify and quantify the components in the analyte. The neural signal processing allows for innovative sampling and analysis strategies to be employed with the microsensor. In most situations, the whole response signature from the voltammogram can be used to identify, classify, and quantify an analyte, without dissecting it into component parts. This allows an instrument to be calibrated once for a specific gas or mixture of gases by simple exposure to a multi-component standard rather than by a series of individual gases. The sampled unknown analytes can vary in composition or in concentration, the calibration, sensing, and processing methods of these active voltammetric microsensors can

  1. Varicose vein stripping

    Science.gov (United States)

    ... vein stripping; Venous reflux - vein stripping; Venous ulcer - veins Images Circulatory system References American Family Physician. Management of varicose veins. www.aafp.org/afp/2008/1201/p1289.html . ...

  2. Voltammetric Behavior of Sodium 7-Methoxyl-4'-hydroxylisoflavone-3'-sulfonate and Its Application

    Institute of Scientific and Technical Information of China (English)

    ZHANG Zun-Ting张尊听; DONG She-Ying董社英; ZHENG Jian-Bin郑建斌; ZHANG Hong-Fang张宏芳; GAO Hong高鸿

    2004-01-01

    Voltammetric behavior of sodium 7-methoxyl-4'-hydroxylisoflavone-3'-sulfonate (SMHS) in the aqueous solution from pH 1 to 5 was studied by linear sweep voltammetry, cyclic voltammetry and normal pulse voltammetry.SMHS caused only one reduction wave at -1.34 V (vs. saturated calomel electrode, SCE), which was an irreversible adsorptive wave of SMHS protonized involving one electron and one proton. The peak current of SMHS on synthetic samples. In addition, its scavenging effect on superoxide anion radical was studied by the auto-oxidation of pyrogallol in HCl-tris buffer solution (pH=8.2) in order to explain its peculiar biological effects. The experimental results proved that SMHS has antioxidant quality, and it is an efficient free radical scavenger of superoxide anion radical.

  3. Voltammetric methods for determination and speciation of inorganic arsenic in the environment-A review

    Energy Technology Data Exchange (ETDEWEB)

    Mays, Douglas E. [Centre for Clean Water and Sustainable Technologies, Department of Chemistry and Biochemistry, George Mason University, Fairfax, VA 20120 (United States); Hussam, Abul, E-mail: ahussam@gmu.edu [Centre for Clean Water and Sustainable Technologies, Department of Chemistry and Biochemistry, George Mason University, Fairfax, VA 20120 (United States)

    2009-07-30

    The measurement of inorganic arsenic in the environment has received considerable attention over the past 40+ years due to its toxicity and prevalence in drinking water. This paper provides an overview of voltammetric techniques used since 2001. More than fifty papers from refereed analytical chemistry journals on the speciation and measurement of inorganic arsenic (As(III) and As(V)) in practical and environmental samples are included. The present review shows that stripping voltammetry is a sensitive and inexpensive technique. The new approaches include development of novel measurement protocols through media variation, development and use of new boron doped diamond electrodes modified with metals, nano Au-modified electrodes on carbon or carbon nano-tubes, novel rotating disc and vibrating electrodes to enhance mass transfer, and modified Hg(l) and thin film Bi on carbon for cathodic stripping voltammetry are discussed. Although, majority of the papers were of exploratory in nature, the trend towards developing a commercial standalone instrument for field use is still in progress.

  4. STUDY OF ELECTROPOLIMERIZATION PROCESSES OF PYRROLE BY CYCLIC VOLTAMMETRIC TECHNIQUE

    Directory of Open Access Journals (Sweden)

    Adhitasari Suratman

    2010-06-01

    Full Text Available Electropolymerization processes and electrochemical properties of polypyrrole as electroactive polymer have been studied by cyclic voltammetric technique. Pyrrole was electropolymerized to form polypyrrole in water-based solvent containing sodium perchlorate as supporting electrolyte in several pH values. The pH of the solutions were varied by using Britton Robinson buffer. The results showed that oxidation potential limit of electropolymerization processes of pyrrole was 1220 mV vs Ag/AgCl reference electrode. It can be seen that cyclic voltammetric respon of polypyrrole membrane that was prepared by electropolymerization processes of pyrrole at the scanning rate of 100 mV/s was stable. While the processes of pyrrole electropolymerization carried out at the variation of pH showed that the best condition was at the pH range of 2 - 6.   Keywords: polypyrolle, electropolymer, voltammetric technique

  5. Microscopic and voltammetric properties of lustrous bismuth deposits

    OpenAIRE

    Krolicka, Agnieszka; Bobrowski, Andrzej; Pamuła, Elżbieta

    2010-01-01

    A comparison of lustrous bismuth films, plated at glassy carbon, platinum and gold supports, is presented. The voltammetric performance of preplated bismuth film electrodes was tested using 50 μg/L In(III) and 50 μg/L Pb(II) solutions in 0.1 M acetic buffer in square wave and differential pulse modes. The influence of support material, plating solution concentration and storing conditions on the voltammetric response of BiFEs is discussed. The results of microscopic examination...

  6. A novel voltammetric sensor for citalopram based on multiwall carbon nanotube/(poly(p-aminobenzene sulfonic acid)/β-cyclodextrin)

    Energy Technology Data Exchange (ETDEWEB)

    Gholivand, Mohammad-Bagher, E-mail: mbgholivand2013@gmail.com; Akbari, Arezoo

    2016-05-01

    Multi-walled carbon nanotube (MWCNTS) coated with poly p-aminobenzene sulfonic acid/β-cyclodextrin (p-ABSA/β-CD) film was used as an effective strategy for modification of the surface of glassy carbon electrode (GCE). Electrochemical study and determination of citalopram (CT) were investigated at the p (p-ABSA)/β-CD/MWCNT/GC using cyclic and differential pulse anodic stripping voltammetric techniques. The results indicate that the p (p-ABSA)/β-CD/MWCNT/GC significantly enhanced the oxidation peak current of CT. The modified electrode was characterized by electrochemical impedance spectroscopy (EIS), scanning electron microscopy(SEM) and cyclic voltammetry (CV).The fabricated electrochemical sensor exhibits a fast and reversible linear response toward CT within the concentration ranges of 90 nM–1 μM, 1–11 μM and 11–100 μM with correlation coefficients greater than 0.99 and detection limit of 44 nM. The resulting functionalized polymer film features interesting electrochemical properties such good recovery, reproducibility and selectivity toward CT. The applicability of the proposed sensor was tested by determination of CT in pharmaceutical combinations and human body fluids. - Highlights: • A novel voltammetric sensor for CT based on p (p-ABSA)/β-CD/MWCNT/GC • Electrochemical study of CT was investigated using CV and DPASV techniques. • This sensor is made easy with good sensitivity and reproducibility. • The method was developed in real sample in the presence of matrix effect.

  7. application of ascorbic acid 2-phosphate as a new voltammetric ...

    African Journals Online (AJOL)

    a

    acid 2-phosphate (AAP) as a new voltammetric substrate has been ... further applied to determine the ALP content in healthy human serum and the results were in ... substrates to produce phenol or p-aminophenol, which is electroactive and can be ... bovine serum, human serum and untreated human blood with the linear ...

  8. Elimination of interferences from surface active substances in voltammetric determination of trace amounts of titanium in environmental water samples

    Directory of Open Access Journals (Sweden)

    Grabarczyk M.

    2013-04-01

    Full Text Available A cathodic stripping voltammetric method for determination of Ti(IV in water samples containing high concentrations of surfactants is described. The linear calibration plot for Ti(IV was achieved in the simultaneous presence of 5 mg L-1 anionic, 1 mg L-1 cationic and 2 mg L-1 nonionic surfactants for an accumulation time of 30 s in the range 2.5 × 10-8 to 5 × 10-7 mol L-1, the detection limit for accumulation time of 30 s was about 8.4 × 10-9 mol L-1. The developed method was successfully applied to Ti(IV determination in environmental waters, such as river water (Bystrzyca, Czerniejówka, stagnant water (Lake Zemborzyce and rain water (collected from eastern areas of Poland with satisfactory results.

  9. Anatomy Comic Strips

    Science.gov (United States)

    Park, Jin Seo; Kim, Dae Hyun; Chung, Min Suk

    2011-01-01

    Comics are powerful visual messages that convey immediate visceral meaning in ways that conventional texts often cannot. This article's authors created comic strips to teach anatomy more interestingly and effectively. Four-frame comic strips were conceptualized from a set of anatomy-related humorous stories gathered from the authors' collective…

  10. Science Comic Strips

    Science.gov (United States)

    Kim, Dae Hyun; Jang, Hae Gwon; Shin, Dong Sun; Kim, Sun-Ja; Yoo, Chang Young; Chung, Min Suk

    2012-01-01

    Science comic strips entitled Dr. Scifun were planned to promote science jobs and studies among professionals (scientists, graduate and undergraduate students) and children. To this end, the authors collected intriguing science stories as the basis of scenarios, and drew four-cut comic strips, first on paper and subsequently as computer files.…

  11. Anatomy Comic Strips

    Science.gov (United States)

    Park, Jin Seo; Kim, Dae Hyun; Chung, Min Suk

    2011-01-01

    Comics are powerful visual messages that convey immediate visceral meaning in ways that conventional texts often cannot. This article's authors created comic strips to teach anatomy more interestingly and effectively. Four-frame comic strips were conceptualized from a set of anatomy-related humorous stories gathered from the authors' collective…

  12. ALICE silicon strip module

    CERN Multimedia

    Maximilien Brice

    2006-01-01

    This small silicon detector strip will be inserted into the inner tracking system (ITS) on the ALICE detector at CERN. This detector relies on state-of-the-art particle tracking techniques. These double-sided silicon strip modules have been designed to be as lightweight and delicate as possible as the ITS will eventually contain five square metres of these devices.

  13. Theoretical and experimental study of redox processes combined with adsorption phenomena under conditions of square-wave voltammetry

    OpenAIRE

    Gulaboski, Rubin

    2001-01-01

    Theoretical models of four electrode reactions coupled with adsorption phenomena under conditions of square-wave voltammetry are developed: simple surface redox reaction, surface catalytic reaction, cathodic stripping reaction of I order, and cathodic stripping reaction of II order.

  14. VOLTAMMETRIC BEHAVIOR OF DOPAMINE AT POLY(4-AMINOPYRIDINE) FILM MODIFIED ELECTRODE AND ITS DETERMINATION BY ADSORPTIVE STRIPPING VOLTAMMETRY%多巴胺在聚对氨基吡啶修饰电极上伏安行为及其溶出伏安法测定

    Institute of Scientific and Technical Information of China (English)

    汪振辉; 张岱; 张岩; 周漱萍

    2000-01-01

    目的大量抗坏血酸(AA)存在下,研究聚对氨基吡啶(POAP)化学修饰膜电极测定神经递质多巴胺(DA).方法用循环伏安和多阶半微分电化学方法研究对氨基吡啶在玻碳电极上的聚合和伏安行为.结果 POAP电极对DA有明显的分子识别和电催化作用.2 000倍AA存在下对DA测定无影响,检测限为4.2×10-11 mol·L-1(富集8 min).结论 POAP电极使用寿命至少长达3个月,DA与AA的氧化峰分开200 mV,可用于大量AA存在下测定神经递质DA.

  15. Fabrication of chitosan-magnetite nanocomposite strip for chromium removal

    Science.gov (United States)

    Sureshkumar, Vaishnavi; Kiruba Daniel, S. C. G.; Ruckmani, K.; Sivakumar, M.

    2016-02-01

    Environmental pollution caused by heavy metals is a serious threat. In the present work, removal of chromium was carried out using chitosan-magnetite nanocomposite strip. Magnetite nanoparticles (Fe3O4) were synthesized using chemical co-precipitation method at 80 °C. The nanoparticles were characterized using UV-visible spectroscopy, fourier transform infrared spectroscopy, X-ray diffraction spectrometer, atomic force microscope, dynamic light scattering and vibrating sample magnetometer, which confirm the size, shape, crystalline nature and magnetic behaviour of nanoparticles. Atomic force microscope revealed that the particle size was 15-30 nm and spherical in shape. The magnetite nanoparticles were mixed with chitosan solution to form hybrid nanocomposite. Chitosan strip was casted with and without nanoparticle. The affinity of hybrid nanocomposite for chromium was studied using K2Cr2O7 (potassium dichromate) solution as the heavy metal solution containing Cr(VI) ions. Adsorption tests were carried out using chitosan strip and hybrid nanocomposite strip at different time intervals. Amount of chromium adsorbed by chitosan strip and chitosan-magnetite nanocomposite strip from aqueous solution was evaluated using UV-visible spectroscopy. The results confirm that the heavy metal removal efficiency of chitosan-magnetite nanocomposite strip is 92.33 %, which is higher when compared to chitosan strip, which is 29.39 %.

  16. Centri-voltammetric study with amberlite XAD-7 resin as a carrier system.

    Science.gov (United States)

    Anik Kirgöz, Ulkü; Tural, Hüseyin; Nil Ertaş, F

    2005-01-15

    Centri-voltammetry is a novel method, which allows combining the advantages of centrifugation and voltammetry. The method offers a practical way for application of coprecipitation in trace analysis allowing direct voltammetric scan hence prevents the loss of the analyte, which usually is the case for other preconcentration techniques. The performance of the method was successfully tested using trace amounts of Pb(2+) ions in aqueous solution in a vessel specially designed to be compatible to both centrifugation and voltammetry. XAD-7 resin was used as the carrier material and the parameters related to the carrier material and medium characteristics as well as the centrifugation settings were investigated. The sensitivity of the method was found comparable to that of stripping techniques and the detection limit for lead ions was calculated as 5.2 x 10(-9)M with mercury coated gold sphere electrode. The precision of the method depends on the configuration of the working electrode and better reproducibility was obtained with mercury coated plate electrodes (R.S.D. 3.3%, n = 6).

  17. Stripping with dry ice

    Science.gov (United States)

    Malavallon, Olivier

    1995-04-01

    Mechanical-type stripping using dry ice (solid CO2) consists in blasting particles of dry ice onto the painted surface. This surface can be used alone or in duplex according to type of substrate to be treated. According to operating conditions, three physical mechanisms may be involved when blasting dry ice particles onto a paint system: thermal shock, differential thermal contraction, and mechanical shock. The blast nozzle, nozzle travel speed, blast angle, stripping distance, and compressed air pressure and media flow rate influence the stripping quality and the uniformity and efficiency obtained.

  18. Voltammetric behavior of ketoconazole and its determination in cosmetic preparation using a β-cyclodextrin modified glassy carbon electrode

    Directory of Open Access Journals (Sweden)

    M.A. El Ries

    2013-06-01

    Full Text Available A voltammetric determination of ketoconazole (KCZ at a beta-cyclo-dextrin modified glassy carbon (CDMGC is described. A large increase in the peak currents was observed in cyclic voltammetry (CV and differential pulse voltammetry (DPV of KCZ. This increase in the big current were attributed to the complex formation of the KCZ with β-cyclodextrin. CV studies indicate that the process is irreversible and adsorption-controlled. The effect of pH, scan rate, cyclodextrin concentration and stability of electrodes on the current responses of KCZ was studied. The linearity was obeyed over the concentration range (1–8 × 10−5 mole/l with a common correlation coefficient and limit of detection of 0.9996 and 10.54 × 10−8, respectively, in pH 9 Britton–Robinson (BR buffer. The modified electrode exhibited good sensitivity, and stability. The voltammetric method was successfully applied for the determination of KCZ in pure solution and in cosmetic preparation under batch condition.

  19. Voltammetric estimation of the content of antibiotics in veterinary preparations

    Directory of Open Access Journals (Sweden)

    Slepchenko Galina

    2016-01-01

    Full Text Available The voltammetric method for determination of tylosin tartrate, gentamicin sulfate, and cefalexin in veterinary preparations was for the first time developed. Electrochemical behavior of these antibiotics on the mercury film electrode was studied, and the working conditions (background electrolyte, deposition potential were defined for getting analytical signals using the voltammetry. The methods of real objects preparation for determination of tylosin tartrate, gentamicin sulfate, and cefalexin were offered. The techniques for the voltammetric determination of antibiotics in the veterinary preparations may be used in cefalexin ranging from 0.1 to 2.0 g/dm3, tylosin tartrate in the range from 0.1 to 1.7 g/dm3, and gentamicin sulfate from 0.1 to 1.5 g/dm3 (Sr is not more than 25 %

  20. Voltammetric estimation of the content of antibiotics in veterinary preparations

    OpenAIRE

    2016-01-01

    The voltammetric method for determination of tylosin tartrate, gentamicin sulfate, and cefalexin in veterinary preparations was for the first time developed. Electrochemical behavior of these antibiotics on the mercury film electrode was studied, and the working conditions (background electrolyte, deposition potential) were defined for getting analytical signals using the voltammetry. The methods of real objects preparation for determination of tylosin tartrate, gentamicin sulfate, and cefale...

  1. New molecular imprinted voltammetric sensor for determination of ochratoxin A

    Energy Technology Data Exchange (ETDEWEB)

    Yola, Mehmet Lütfi, E-mail: mehmetyola@gmail.com [Department of Metallurgical and Materials Engineering, Faculty of Engineering, Sinop University, Sinop (Turkey); Gupta, Vinod Kumar, E-mail: vinodfcy@iitr.ac.in [Indian Institute of Technology, Department of Chemistry, Roorkee, Roorkee 247667 (India); Department of Applied Chemistry, University of Johannesburg, Johannesburg (South Africa); Atar, Necip [Department of Chemical Engineering, Faculty of Engineering, Pamukkale University, Denizli (Turkey)

    2016-04-01

    In this report, a novel molecular imprinted voltammetric sensor based on silver nanoparticles (AgNPs) involved in a polyoxometalate (H{sub 3}PW{sub 12}O{sub 40}, POM) functionalized reduced graphene oxide (rGO) modified glassy carbon electrode (GCE) was presented for determination of ochrattoxin A (OCH). The developed surfaces were characterized using scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) method. OCH imprinted GCE was prepared via electropolymerization process of 100 mM phenol as monomer in the presence of phosphate buffer solution (pH 6.0) containing 25 mM OCH. The linearity range and the detection limit of the method were calculated as 5.0 × 10{sup −11} − 1.5 × 10{sup −9} M and 1.6 × 10{sup −11} M, respectively. The voltammetric sensor was applied to grape juice and wine samples with good selectivity and recovery. The stability of the voltammetric sensor was also reported. - Highlights: • Ochratoxin A-imprinted electrochemical sensor is developed for the sensitive detection of ochratoxin A • The nanomaterial and ochratoxin A-imprinted surfaces were characterized by several methods • Ochratoxin A-imprinted electrochemical sensor is sensitive and selective in analysis of food • Ochratoxin A-imprinted electrochemical sensor is preferred to the other methods.

  2. Estudo voltamétrico do complexo de cobre(II com o ligante vermelho de alizarina S, adsorvido na superfície do eletrodo de grafite pirolítico Voltammetric study of complex of copper (II with alizarin red S ligand, absorbed on surface of pyrolytic graphite electrode

    Directory of Open Access Journals (Sweden)

    Victor E. Mouchrek Filho

    1999-06-01

    Full Text Available The alizarin red S (ARS has been used as a spectrophotometric reagent of several metals for a long time. Now this alizarin has been used as modifier agent of electrodes, for voltammetric analyses. In this work cyclic voltammetry experiments was accomplished on closed circuit, with the objective of studying the voltammetric behavior of alizarin red S adsorbed and of its copper complex, on the surface of the pyrolytic graphite electrode. These studies showed that ARS strongly adsorbs on the surface of this electrode. This adsorption was used to immobilize ions copper(II from the solution.

  3. Electrodeposited apatite coating for solid-phase microextraction and sensitive indirect voltammetric determination of fluoride ions.

    Science.gov (United States)

    Mao, Yuehong; Chen, Yufei; Chu, Lin; Zhang, Xiaoli

    2013-10-15

    Electrodeposition was used to prepare a new solid phase microextraction (SPME) coatings. Two apatite SPME coatings, dicalcium phosphate dihydrate (DCPD or brushite) and hydroxyapatite (HAP) were validly and homogeneously one-step electrodeposited on glassy carbon electrode (GCE) under different conditions. The coatings were characterized by XRD, FTIR, SEM, CV and EIS. The apatite SPME coatings showed excellent and selective adsorbability to fluoride ions. A novel indirect voltammetric strategy for sensitive detection of fluoride was proposed using K3Fe(CN)6 as indicating probe. The detection principle of fluoride ions was based on the increment of steric hindrance after fluoride adsorption, which resulting in the decrease of the amperometric signal to Fe(CN)6(3-). The liner ranges were 0.5-20.0 μmol/L for n-DCPD/GCE with the limit of detection of 0.14 μmol/L and 0.1-50.0 μmol/L for n-HAP/GCE with the limit of detection of 0.069 μmol/L, respectively. The developed method was applied to the analysis of water samples (lake, spring and tap water) and the recovery values were found to be in the range of 90-106%.

  4. Electrochemical Investigation of Catechol at Poly(niacinamide Modified Carbon Paste Electrode: A Voltammetric Study

    Directory of Open Access Journals (Sweden)

    A. B. Teradale

    2016-01-01

    Full Text Available A polymeric thin film modified electrode, that is, poly(niacinamide modified carbon paste electrode (MCPE, was developed for the electrochemical determination of catechol (CC by using cyclic voltammetric technique. Compared to bare carbon paste electrode (BCPE, the poly(niacinamide MCPE shows good electrocatalytic activity towards the oxidation of catechol in phosphate buffer solution (PBS of physiological pH 7.4. All experimental parameters were optimized. Poly(niacinamide modified carbon paste electrode gave a linear response between concentration of CC and its anodic peak current in the range within 20.6–229.0 μM. The limit of detection (3S/M and limit of quantification (10S/M were 1.497 μM and 4.99 μM, respectively. From the study of scan rate variation, the electrode process was found to be adsorption-controlled. The involvement of protons and electrons in the oxidation of CC was found to be equal. The probable electropolymerisation mechanism of niacinamide was proposed. Finally, this method can be used in development of a sensor for sensitive determination of CC.

  5. Improvement of the ultra-trace voltammetric determination of Rh in environmental samples using signal transformation.

    Science.gov (United States)

    Almécija, C; Cobelo-García, A; Santos-Echeandía, J

    2016-01-01

    Rhodium (Rh) is present at the Earth's surface at ultra-trace concentrations (0.06 ng g(-1)); however, its use in catalytic converters has increased its deposition nearby traffic pressure and therefore the interest in analytical techniques for Rh determination has raised in the recent years. In this study we propose an improvement of Rh measurement by adsorptive voltammetry applying second-derivative signal transformation. The optimization of experimental parameters affecting the voltammetric analysis were carried out using sediment samples; these include the amount of sample digest used, the hydrochloric acid and formaldehyde concentrations, deposition potential and equilibration time. The use of the second derivative transformation provided well-defined peaks due to the minimization of background interferences, leading to a significant decrease in the detection limits. Accordingly, a detection limit of 200 fM Rh in the cell was obtained, which corresponds to 14 pg g(-1) of Rh for 200mg of sediments. The optimized methodology was applied to the analysis of Rh in a sediment core collected close to a motorway bridge from Tagus Estuary (Lisbon, Portugal). Here, Rh concentrations ranged from 0.06 to 0.47 ng g(-1), showing a surface Rh-enrichment linked to traffic, which was consistent with a Pt superficial peak. Reference materials were also analyzed, including road dust (BCR-723) and river sediment (JSD-2), and values obtained were in agreement with certified concentrations and previously values reported in the literature. Copyright © 2015 Elsevier B.V. All rights reserved.

  6. Biochar prepared from castor oil cake at different temperatures: A voltammetric study applied for Pb(2+), Cd(2+) and Cu(2+) ions preconcentration.

    Science.gov (United States)

    Kalinke, Cristiane; Mangrich, Antonio Sálvio; Marcolino-Junior, Luiz H; Bergamini, Márcio F

    2016-11-15

    Biochar is a carbonaceous material similar produced by pyrolysis of biomass under oxygen-limited conditions. Pyrolysis temperature is an important parameter that can alters biochar characteristics (e.g. surface area, pore size distribution and surface functional groups) and affects it efficacy for adsorption of several probes. In this work, biochar samples have been prepared from castor oil cake using different temperatures of pyrolysis (200-600°C). For the first time, a voltammetric procedure based on carbon paste modified electrode (CPME) was used to investigate the effect of temperature of pyrolysis on the adsorptive characteristics of biochar for Pb(II), Cd(II) and Cu(II) ions. Besides the electrochemical techniques, several characterizations have been performed to evaluate the physicochemical properties of biochar in function of the increase of the pyrolysis temperature. Results suggest that biochar pyrolized at 400°C (BC400) showed a better potential for ions adsorption. The CPME modified with BC400 showed better relative current signal with adsorption affinity: Pb(II)>Cd(II)>Cu(II). Kinetic studies revealed that the pseudo-second order model describes more accurately the adsorption process suggesting that the surface reactions control the adsorption rate. Values found for amount adsorbed were 15.94±0.09; 4.29±0.13 and 2.38±0.39μgg(-1) for Pb(II), Cd(II) and Cu(II) ions, respectively.

  7. Increased sensitivity of anodic stripping voltammetry at the hanging mercury drop electrode by ultracathodic deposition

    Energy Technology Data Exchange (ETDEWEB)

    Rodrigues, Jose A.; Rodrigues, Carlos M.; Almeida, Paulo J.; Valente, Ines M.; Goncalves, Luis M. [Requimte - Departamento de Quimica e Bioquimica, Faculdade de Ciencias, Universidade do Porto, Rua do Campo Alegre, no. 687, 4169-007 Porto (Portugal); Compton, Richard G. [Department of Chemistry, Physical and Theoretical Chemistry Laboratory, Oxford University, South Parks Road, Oxford OX1 3QZ (United Kingdom); Barros, Aquiles A., E-mail: ajbarros@fc.up.pt [Requimte - Departamento de Quimica e Bioquimica, Faculdade de Ciencias, Universidade do Porto, Rua do Campo Alegre, no. 687, 4169-007 Porto (Portugal)

    2011-09-09

    Highlights: {yields} At very cathodic accumulation potentials (overpotential deposition) the voltammetric signals of Zn{sup 2+}, Cd{sup 2+}, Pb{sup 2+} and Cu{sup 2+} increase. {yields} 5 to 10-fold signal increase is obtained. {yields} This effect is likely due to mercury drop oscillation at such cathodic potentials. {yields} This effect is also likely due to added local convection at the mercury drop surface caused by the evolution of hydrogen bubbles. - Abstract: An improved approach to the anodic stripping voltammetric (ASV) determination of heavy metals, using the hanging mercury drop electrode (HMDE), is reported. It was discovered that using very cathodic accumulation potentials, at which the solvent reduction occurs (overpotential deposition), the voltammetric signals of zinc(II), cadmium(II), lead(II) and copper(II) increase. When compared with the classical methodology a 5 to 10-fold signal increase is obtained. This effect is likely due to both mercury drop oscillation at such cathodic potentials and added local convection at the mercury drop surface caused by the evolution of hydrogen bubbles.

  8. micro strip gas chamber

    CERN Multimedia

    1998-01-01

    About 16 000 Micro Strip Gas Chambers like this one will be used in the CMS tracking detector. They will measure the tracks of charged particles to a hundredth of a millimetre precision in the region near the collision point where the density of particles is very high. Each chamber is filled with a gas mixture of argon and dimethyl ether. Charged particles passing through ionise the gas, knocking out electrons which are collected on the aluminium strips visible under the microscope. Such detectors are being used in radiography. They give higher resolution imaging and reduce the required dose of radiation.

  9. [Post-stripping telangiectasis].

    Science.gov (United States)

    Hutinel, B; Maraval, M

    1985-01-01

    These telangiectasia appear between one and six months after the operation, especially in cases of capillary fragility. The most common localizations are the antero-internal and external sides of the thighs and knees. Unnecessary strippings, of continent saphenous veins, are the most frequent cause of these. Their prevention consists of the least possible traumatising stripping, using a fine stripper, a very rigorous post-operative support, and the wearing of light varicose stockings or tights for between one and three months. The treatment using microsclerosis, often delicate, should not be undertaken before six months.

  10. Electrochemical Quartz Crystal Microbalance Monitoring of the Cyclic Voltammetric Deposition of Polyaniline

    Science.gov (United States)

    Xie, Qingji; Li, Zhili; Deng, Chunyan; Liu, Meiling; Zhang, Youyu; Ma, Ming; Xia, Shaoxi; Xiao, Xiaoming; Yin, Dulin; Yao, Shouzhuo

    2007-01-01

    A real-time, labeled-free and nanogram-sensitive mass sensor, electrochemical quartz crystal microbalance (EQCM) is used to monitor a cyclic voltammetric deposition of polyaniline (PANI). The results determined that the efficiency for PANI deposition and the anion-doping ratio is calculated in one single cyclic voltammetric.

  11. Resistance to oxidation of white wines assessed by voltammetric means.

    Science.gov (United States)

    Rodrigues, Astride; Silva Ferreira, A C; Guedes de Pinho, Paula; Bento, Fátima; Geraldo, Dulce

    2007-12-26

    This work concerns the development of a methodology suited to measure the resistance to oxidation of white wines by cyclic voltammetry. The voltammetric responses of several white wines of different origin and age were analyzed in the oxidation potential range (0.2-1.2 V vs SCE). Currents measured at fixed potentials were correlated to the concentration of ascorbic acid, SO2, and total phenolics. A forced degradation study was monitored by cyclic voltammetry; from plots of current versus time, the consumption rates of oxidizable species in wine were estimated.

  12. ALICE Silicon Strip Detector

    CERN Multimedia

    Nooren, G

    2013-01-01

    The Silicon Strip Detector (SSD) constitutes the two outermost layers of the Inner Tracking System (ITS) of the ALICE Experiment. The SSD plays a crucial role in the tracking of the particles produced in the collisions connecting the tracks from the external detectors (Time Projection Chamber) to the ITS. The SSD also contributes to the particle identification through the measurement of their energy loss.

  13. Voltammetric detection of biological molecules using chopped carbon fiber.

    Science.gov (United States)

    Sugawara, Kazuharu; Yugami, Asako; Kojima, Akira

    2010-01-01

    Voltammetric detection of biological molecules was carried out using chopped carbon fibers produced from carbon fiber reinforced plastics that are biocompatible and inexpensive. Because chopped carbon fibers normally are covered with a sizing agent, they are difficult to use as an electrode. However, when the surface of a chopped carbon fiber was treated with ethanol and hydrochloric acid, it became conductive. To evaluate the functioning of chopped carbon fibers, voltammetric measurements of [Fe(CN)(6)](3-) were carried out. Redoxes of FAD, ascorbic acid and NADH as biomolecules were recorded using cyclic voltammetry. The sizing agents used to bundle the fibers were epoxy, polyamide and polyurethane resins. The peak currents were the greatest when using the chopped carbon fibers that were created with epoxy resins. When the electrode response of the chopped carbon fibers was compared with that of a glassy carbon electrode, the peak currents and the reversibility of the electrode reaction were sufficient. Therefore, the chopped carbon fibers will be useful as disposable electrodes for the sensing of biomolecules.

  14. Sono-cathodic stripping voltammetry of manganese at a polished boron-doped diamond electrode: application to the determination of manganese in instant tea.

    Science.gov (United States)

    Saterlay, A J; Foord, J S; Compton, R G

    1999-12-01

    Ultrasonically assisted cathodic stripping voltammetry at a boron-doped diamond electrode was developed for the detection of manganese. Differential-pulse voltammetry was used to give the analytical signal from a cathodic strip of electrodeposited MnO2; linearity was observed from 10(-11) M to at least 3 x 10(-7) M, with 10(-11) M being the detection limit for a 2 min deposition. The procedure involves both ultrasonic-anodic deposition of MnO2 and ultrasonic-cathodic stripping. This novel analytical tool is robust, reproducible, mercury free, oxygen insensitive and highly specific towards manganese. The differential-pulse sono-cathodic stripping voltammetric technique was used to determine successfully the manganese content of two instant tea samples, giving excellent agreement with independent AAS analyses.

  15. Anodic Stripping Voltammetry with Pencil Graphite Electrode for Determination of Chromium (III)

    Science.gov (United States)

    Wyantuti, S.; Hafidza, R. A.; Ishmayana, S.; Hartati, Y. W.

    2017-02-01

    Chromium is required as micronutrient that has roles in insulin metabolism and blood glucose level regulation. Chromium (III) deficiency can cause hyperglycemia and glycosuria. However, a high amount of chromium in body can cause allergic reaction, organ damage, and even death because of its toxicity. Chromium is commonly used in steel industries. Simultaneously with the development of industry, the waste disposal that can endanger environment also increased. Therefore, a sensitive and specific analysis method for chromium detection is required. Stripping voltammetry is one of the voltammetric methods that is commonly used for heavy metal analysis due to the very low limit of detection (sub ppb). The present study was conducted to develop an analysis method for chromium (III) determination using pencil graphite electrode. Quantitative determination was performed for chromium (III) which measured at -0.8 to +1.0 V with deposition time for 60 s and 50 mV/s scan rate. Stripping voltammetric analysis of chromium (III) using pencil graphite electrode gave linear range at 12.5 to 75 ppm with limit of detection of 0.31 ppm.

  16. Parabolic Strip Telescope

    CERN Document Server

    Chadzitaskos, Goce

    2013-01-01

    We present a proposal of a new type of telescopes using a rotating parabolic strip as the primary mirror. It is the most principal modification of the design of telescopes from the times of Galileo and Newton. In order to demonstrate the basic idea, the image of an artificial constellation observed by this kind of telescope was reconstructed using the techniques described in this article. As a working model of this new telescope, we have used an assembly of the primary mirror---a strip of acrylic glass parabolic mirror 40 cm long and 10 cm wid shaped as a parabolic cylinder of focal length 1 m---and an artificial constellation, a set of 5 apertures in a distance of 5 m illuminated from behind. In order to reconstruct the image, we made a series of snaps, each after a rotation of the constellation by 15 degrees. Using Matlab we reconstructed the image of the artificial constellation.

  17. Investigation on Voltammetric Behavior of Camptothecin and Its Analytical Application

    Institute of Scientific and Technical Information of China (English)

    ZHENG, Jian-Bin; MENG, Zu-Chao; LIU, Bo; ZHANG, Hong-Fang

    2006-01-01

    The voltammetric behavior of camptothecin (CPT) in Britton-Robinson (B-R) buffer solutions (pH 2.09-9.07)was studied by the means of linear sweep voltammetry (LSV), cyclic voltammetry (CV) and normal pulse voltammetry (NPV) at a hanging mercury drop electrode. In different pH range of B-R buffer solutions, CPT could cause three reduction waves. In B-R buffer solutions (pH 2.09-5.46), wave P1 yielded by CPT was a two-electron wave.Between pH 6.01 and 9.07, CPT could yield two reduction waves P2 and P3. In addition, the pure CPT obtained from camptotheca acumina grown only in China was determined by NPV, and a linear response was observed in the tion limit for CPT.

  18. XCII. A Low-Cost Voltammetric Signal Generator for the Electroanalytical Chemistry Laboratory

    Science.gov (United States)

    Ewing, Galen W., Ed

    1977-01-01

    Describes the construction of a versatile signal generator suitable for use in cyclic voltammetric experiments, which can also be adapted to a conventional dc polarograph by replacing its ramp source. (MLH)

  19. Voltammetric scanning electrochemical cell microscopy: dynamic imaging of hydrazine electro-oxidation on platinum electrodes

    NARCIS (Netherlands)

    Chen, C.-H.; Jacobse, L.; McKelvey, K.; Lai, S.C.S.; Koper, M.T.M.; Unwin, P.R.

    2015-01-01

    Voltammetric scanning electrochemical cell microscopy (SECCM) incorporates cyclic voltammetry measurements in the SECCM imaging protocol, by recording electrochemical currents in a wide potential window at each pixel in a map. This provides much more information compared to traditional fixed potenti

  20. Spray Rolling Aluminum Strip

    Energy Technology Data Exchange (ETDEWEB)

    Lavernia, E.J.; Delplanque, J-P; McHugh, K.M.

    2006-05-10

    Spray forming is a competitive low-cost alternative to ingot metallurgy for manufacturing ferrous and non-ferrous alloy shapes. It produces materials with a reduced number of processing steps, while maintaining materials properties, with the possibility of near-net-shape manufacturing. However, there are several hurdles to large-scale commercial adoption of spray forming: 1) ensuring strip is consistently flat, 2) eliminating porosity, particularly at the deposit/substrate interface, and 3) improving material yield. Through this program, a new strip/sheet casting process, termed spray rolling, has been developed, which is an innovative manufacturing technique to produce aluminum net-shape products. Spray rolling combines the benefits of twin-roll casting and conventional spray forming, showing a promising potential to overcome the above hurdles associated with spray forming. Spray rolling requires less energy and generates less scrap than conventional processes and, consequently, enables the development of materials with lower environmental impacts in both processing and final products. Spray Rolling was developed as a collaborative project between the University of California-Davis, the Colorado School of Mines, the Idaho National Engineering and Environmental Laboratory, and an industry team. The following objectives of this project were achieved: (1) Demonstration of the feasibility of the spray rolling process at the bench-scale level and evaluation of the materials properties of spray rolled aluminum strip alloys; and (2) Demonstration of 2X scalability of the process and documentation of technical hurdles to further scale up and initiate technology transfer to industry for eventual commercialization of the process.

  1. Mesoporous film of WO3-the "sunlight" assisted decomposition of surfactant in wastewater for voltammetric determination of Pb

    Science.gov (United States)

    Krasnodębska-Ostręga, Beata; Bielecka, Agnieszka; Biaduń, Ewa; Miecznikowski, Krzysztof

    2016-12-01

    In this paper we present the application of "sunlight" assisted digestion in the presence of WO3 to the decomposition of dissolved organic matter, using the anionic surfactant sodium dodecyl sulfate (SDS) and the nonionic surfactant (1,1,3,3-tetramethylbutyl)phenyl-polyethylene glycol (Triton™X-114) in natural water samples, prior to the determination of traces residues of lead by stripping voltammetry methods. The results of the study showed firstly that the preparation of reproducible WO3 layers characterized by high mechanical and chemical resistance was possible, and secondly that it was also possible to obtain a high efficiency of decomposition, equal in efficiency to that of the reference method, which was the hydrogen peroxide oxidation assisted by UV, with evaporation nearly to dryness. The developed procedure is suggested to be a no-reagents method for the decomposition of added SDS, leading to 100% recovery of added Pb (II). The anodic stripping voltammetric curves recorded in solution after 4 h irradiation with UV assisted by WO3 were repeatable and increased linearly with standard additions, but the data finally obtained were incorrect. The curves recorded in solution after "sunlight" assisted digestion in the presence of WO3 were repeatable, and increased linearly with an increasing of concentration of standard additions (100% recovery of Pb). In the case of a nonionic surfactant, the decomposition time is at least 6 h. The advantage of the proposed method is the fact that the digestion process does not need the addition of any chemicals for the complete decomposition of organic matter.

  2. Discrimination of Rice with Different Pretreatment Methods by Using a Voltammetric Electronic Tongue

    OpenAIRE

    2015-01-01

    In this study, an application of a voltammetric electronic tongue for discrimination and prediction of different varieties of rice was investigated. Different pretreatment methods were selected, which were subsequently used for the discrimination of different varieties of rice and prediction of unknown rice samples. To this aim, a voltammetric array of sensors based on metallic electrodes was used as the sensing part. The different samples were analyzed by cyclic voltammetry with two sample-p...

  3. Voltammetric behavior, biocidal effect and synthesis of some new nanomeric fused cyclic thiosemicarbazones and their mercuric(II salts

    Directory of Open Access Journals (Sweden)

    M.S.T. Makki

    2014-11-01

    Full Text Available New nanomeric 3-thioxo-5-methoxy-4,5-dihydro-6-methyl-9-unsubstituted/substituted-1,2,4-triazino[5,6-b]indoles (2a–c and 3-thioxo-5-methoxy-4,5-dihydro-6,7-dihydroxy-1,2,4-triaino[5,6]-cyclobut-6-ene (3 were prepared via reaction of thiosemicarbazide with 5-unsubstitutedand/substituted-indol-2,3-diones and/or 3,4-dihydroxycyclobutane-1,2-dione in methanol–concentrated HCl at room temperature. A series of mercury(II–ligand salts e.g. compound 4b and Hg(II complexes 5a,b and 6 of cyclic Schiff base were prepared. Structures of these compounds were established by elemental analysis and spectral measurements. The redox characteristics of selected compounds were studied for use as chelating agents for stripping voltammetric determination of mercuric(II ions in aqueous media. The compounds were also screened for their use as molluscicidal agents against Biomophalaria Alexandrina Snails responsible for Bilhariziasis.

  4. Sensitive voltammetric determination of tryptophan using an acetylene black paste electrode modified with a Schiff's base derivative of chitosan.

    Science.gov (United States)

    Deng, Peihong; Fei, Junjie; Feng, Yonglan

    2011-12-21

    Chitosan was modified by salicylaldehyde via Schiff's base reaction and the resulting product was modified on the surface of an acetylene black paste electrode (ABPE) by the drop-coating method. In 0.5 mol L(-1) acetate buffer (pH 4.2), a substantial increase in the anodic stripping peak current of tryptophan (Trp) (compared to conventional bare carbon paste electrode (CPE) and bare ABPE) is observed at the Schiff's base chitosan-modified electrode. The parameters influencing voltammetric determination of Trp have been optimized. Under the selected conditions, the linearity between the anodic peak currents and concentrations of Trp demonstrated a wide range of 6.0 × 10(-8) mol L(-1) to 2.0 × 10(-6) mol L(-1), 2.0 × 10(-6) mol L(-1) to 4.0 × 10(-5) mol L(-1) and 4.0 × 10(-5) mol L(-1) to 1.0 × 10(-4) mol L(-1), a low detection limit of 2.0 × 10(-9) mol L(-1) was obtained after a 60 s accumulation. In addition, the developed electrochemical sensor has been successfully applied for the determination of Trp in pharmaceutical and biological samples with satisfactory assay results.

  5. Strip shape control capability of hot wide strip rolling mills

    Institute of Scientific and Technical Information of China (English)

    Renzhong Wang; Quan Yang; Anrui He; Jian Shao; Haitao Bian

    2008-01-01

    The elasticity deformation of rolls was analyzed by means of two-dimensional f'mite element method (FEM) with vari-able thickness. Three typical mills were used as objects for analysis. A thorough study was done on the control capabilities of these mills on the strip shape. Then the strip shape control capabilities of the three mills was compared synthetically.

  6. Lateral interactions and enhanced adsorption

    Science.gov (United States)

    Rikvold, Per Arne; Deakin, Mark R.

    1991-06-01

    We extend earlier work on the effects of lateral adsorbate-adsorbate interactions in systems with two different adsorbate species to consider in detail enhanced adsorption phenomena. We give a detailed explanation of the enhancement mechanism for a lattice-gas model in thermodynamic equilibrium, and provide explicit quantitative criteria which must be satisfied by the effective lateral interactions in systems exhibiting strong, intermediate, or weak enhancement behavior. It is the examination and understanding of the topological details of the ground-state and phase diagrams of the model that allow the formulation of these criteria. The theoretically obtained criteria are supported by precise numerical calculations (transfer-matrix with strip width six) of adsorption isotherms for a three-state lattice-gas model with nearest-neighbor interactions on a triangular lattice. The applicability of this theoretical framework is illustrated by an analysis of experimental adsorption isotherms for the electrochemical adsorption of naphthalene on copper and n-decylamine on nickel, previously obtained by Bockris et al. As suggested by Damaskin et al. we attribute the potential dependence of the organic coverage to the influence of coadsorbed hydrogen. We find that nonlinear least-squares fits of numerical lattice-gas isotherms to the experimental data produce good agreement between the experimental and numerical adsorption isotherms, as well as effective lattice-gas interaction energies consistent with independent estimates from the literature.

  7. Electrochemical studies of 1,5-dihydroxynaphthalene as substrate for voltammetric enzyme immunoassay

    Institute of Scientific and Technical Information of China (English)

    JIAO Kui; YAO Hong; XU Jin; ZHANG Shusheng

    2004-01-01

    A sensitive voltammetric enzyme immunoanalytical method is described for assay of horseradish peroxidase (HRP), labelled-HRP and antigen:antibody:labelled-HRP conjugate (Ag︰AB︰IgG-HRP) using 1,5-dihydroxynaphthalene (1,5-DHN) as substrate. 1,5-DHN is an electrochemical inactive substance, but it may be oxidized by O2 in air to 5-hydroxy-1,4-naphtho- quinone in basic solution, which produces a well-defined voltammetric reduction peak. After adding H2O2 and HRP, HRP catalyzes H2O2 oxidizing 5-hydroxy-1,4-naphthoquinone to 3-hydroxyphthalic acid, leading to the decrease of the voltammetric reduction peak, with which the activity of HRP and the labelled-HRP, further the antigen and antibody may be determined. The mechanism of this voltammetric enzyme-linked immunoassay system is different from the previous reports, in which there are no voltammetric reduction peaks before the addition of H2O2 and HRP, and the reduction peaks appear after the addition of H2O2 and HRP. The height of the voltammetric peak is directly proportional to the concentration of HRP in the previous systems, while the decrease of the voltammetric peak is linear with the concentration of HRP in this system. This new electrochemical method is combined with an indirect enzyme immunoassay using direct antigen-coating format for the detection of the purified tobacco mosaic virus (TMV) with a linear range from 25.0 to 340.0 ng/mL, and a detection limit 25.0 ng/mL.

  8. Anodic stripping voltammetry at in situ bismuth-plated carbon and gold microdisc electrodes in variable electrolyte content unstirred solutions.

    Science.gov (United States)

    Baldrianova, L; Svancara, I; Economou, A; Sotiropoulos, S

    2006-10-27

    Carbon and gold microdisc electrodes (30 and 10 microm, respectively) have been tested as substrates for in situ bismuth film plating from unstirred solutions of variable acetate buffer content and were subsequently used in the anodic stripping voltammetry determination of Pb(II) and Cd(II) ions. The effects of Bi(III) concentration, analyte accumulation time, stirring as well as supporting electrolyte content have been studied. Under optimal conditions good voltammetric responses were obtained by means of square wave anodic stripping voltammetry in unstirred analyte solutions of 5 x 10(-8) to 10(-6)M, even in the absence of added buffer. In an indicative application, Pb(II) ion levels were determined in tap water using bismuth-plated carbon microdisc electrodes.

  9. Electropolymerized supramolecular tetraruthenated porphyrins applied as a voltammetric sensor

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Monize M. da; Ribeiro, Gabriel H.; Faria, Anizio M. de; Bogado, Andre L.; Dinelli, Luis R., E-mail: dinelli@pontal.ufu.br [Universidade Federal de Uberlandia (UFU), Ituiutaba, MG (Brazil). Faculdade de Ciencias Integradas do Pontal; Batista, Alzir A. [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil). Departamento de Quimica

    2013-11-15

    Porphyrin 5,10,15,20-Tetra(4-pyridyl)manganese(III), [Mn-TPyP(H{sub 2}O){sub 2}]PF{sub 6}, and electropolymerized supramolecular porphyrins (ESP), {l_brace}Mn-TPyP(H{sub 2}O){sub 2}[RuCl{sub 3}(dppb)]{sub 4}{r_brace}PF{sub 6} (dppb = 1,4-bis(diphenylphosphine)butane), were synthesized and characterized. A thin solid film of ESP was obtained on a glass carbon electrode surface by a cyclic voltammetry method. The peak current increased with the number of voltammetric cycles, which shows a typical behavior of the species being adsorbed on the surface of the electrode. Cyclic voltammetry was also employed for acetaminophen quantification using an ESP modified electrode. The modified electrode shows a linear relationship between the anodic peak current and the concentration of acetaminophen (in the rage 0.05 to 0.7 mmol L{sup -1}. The performance of the modified electrode was verified by the determination of acetaminophen in a commercial pharmaceutical product and the results were in good agreement with those obtained by a control HPLC method. (author)

  10. Differential pulse voltammetric assay of lercanidipine in tablets.

    Science.gov (United States)

    Alvarez-Lueje, Alejandro; Pujol, Sara; Núñez-Vergara, Luis J; Squella, Juan A

    2002-01-01

    Lercanidipine in ethanol-0.04M Britton-Robinson buffer (20 + 80) gives an irreversible anodic response on a glassy carbon electrode in a broad pH range (2-12) that depends on pH. This signal can be attributed to oxidation of the 1,4-dihydropyridine ring to give the corresponding pyridine derivative. For analytical purposes, differential pulse voltammetry at pH 4 was selected. Under these conditions, good values of both within- and interday reproducibility were obtained, with coefficient of variation (CV) values of 1.56 and 1.70%, respectively, for 10 successive runs. For quantitation, the calibration curve method was used for lercanidipine concentrations ranging from 1 x 10(-5) to 1 x 10(-4) M. The detection and quantitation limits were 1.39 x 10(-5) and 1.49 x 10(-5), respectively. A liquid chromatographic method with electrochemical detection was used for comparison. The voltammetric method showed good selectivity with respect to both excipients and degradation products. The recovery study exhibited a CV of 0.94% and an average recovery of 98.3%, and it was not necessary to treat the sample before the analysis. The method was successfully applied to the individual tablet assay of lercanidipine in commercial tablets.

  11. Analysis/design of strip reinforced random composites (strip hybrids)

    Science.gov (United States)

    Chamis, C. C.; Sinclair, J. H.

    1978-01-01

    Advanced analysis methods and composite mechanics were applied to a strip-reinforced random composite square panel with fixed ends to illustrate the use of these methods for the a priori assessment of the composite panel when subjected to complex loading conditions. The panel was assumed to be of E-glass random composite. The strips were assumed to be of three advanced unidirectional composites to cover a range of low, intermediate, and high modulus stiffness. The panels were assumed to be subjected to complex loadings to assess their adequacy as load-carrying members in auto body, aircraft engine nacelle and windmill blade applications. The results show that strip hybrid panels can be several times more structurally efficient than the random composite base materials. Some of the results are presented in graphical form and procedures are described for use of these graphs as guides for preliminary design of strip hybrids.

  12. Analysis/design of strip reinforced random composites /strip hybrids/

    Science.gov (United States)

    Chamis, C. C.; Sinclair, J. H.

    1978-01-01

    Results are described which were obtained by applying advanced analysis methods and composite mechanics to a strip-reinforced random composite square panel with fixed ends. This was done in order to illustrate the use of these methods for the apriori assessment of the composite panel when subjected to complex loading conditions. The panel was assumed to be of E-Glass/Random Composite. The strips were assumed to be of three advanced unidirectional composites to cover a range of low, intermediate, and high modulus stiffness. The panels were assumed to be subjected to complex loadings to assess their adequacy as load-carrying members in auto body, aircraft engine nacelle, and windmill blade applications. The results show that strip hybrid panels can be several times more structurally efficient than the random composite base materials. Some of the results are presented in graphical form and procedures are described for use of these graphs as guides for preliminary design of strip hybrids.

  13. Application of renewable silver amalgam annular band electrode to voltammetric determination of vitamins C, B1 and B2.

    Science.gov (United States)

    Baś, Bogusław; Jakubowska, Małgorzata; Górski, Łukasz

    2011-05-30

    In this work, the design and results of applying silver liquid amalgam film-modified silver solid amalgam annular band electrode (AgLAF-AgSAE), refreshed before each measurement, to voltammetric determination of vitamins C (VC), B(1) (VB1) and B(2) (VB2) are presented. The method is based on adsorptive accumulation of analytes at the AgLAF-AgSAE in a phosphate buffer (VB1), phosphate buffer with Triton X-100 (VB2) and an alkaline borate buffer with Triton X-100 (VC). The analytical parameters and procedure of electrode activation were optimized. The calibration graphs obtained for vitamins C, B(1) and B(2) are linear, respectively, for concentration range 0.05-12, 0.01-0.1 and 0.05-3 mg L(-1). The detection limits were calculated and equaled 0.02, 0.003 and 0.009 mg L(-1), while repeatability of the peak current was 2%, 1% and 3%, respectively. These results are comparable with results obtained for polarographic determination of the same vitamins using mercury electrodes. Finally, the AgLAF-AgSAE was applied to the determination of vitamins in pharmaceutical samples and fruit juices with satisfactory results.

  14. Voltammetric studies of Azathioprine on the surface of graphite electrode modified with graphene nanosheets decorated with Ag nanoparticles.

    Science.gov (United States)

    Asadian, Elham; Iraji Zad, Azam; Shahrokhian, Saeed

    2016-01-01

    By using graphene nanosheets decorated with Ag nanoparticles (AgNPs-G) as an effective approach for the surface modification of pyrolytic graphite electrode (PGE), a sensing platform was fabricated for the sensitive voltammetric determination of Azathioprine (Aza). The prepared AgNPs-G nanosheets were characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), UV-vis and Raman spectroscopy techniques. The electrochemical behavior of Aza was investigated by means of cyclic voltammetry. Comparing to the bare PGE, a remarkable enhancement was observed in the response characteristics of Aza on the surface of the modified electrode (AgNPs-G/PGE) as well as a noticeable decrease in its reduction overpotential. These results can be attributed to the incredible enlargement in the microscopic surface area of the electrode due to the presence of graphene nanosheets together with strong adsorption of Aza on its surface. The effect of experimental parameters such as accumulation time, the amount of modifier suspension and pH of the supporting electrolyte were also optimized toward obtaining the maximum sensitivity. Under the optimum conditions, the calibration curve studies demonstrated that the peak current increased linearly with Aza concentrations in the range of 7 × 10(-7) to 1 × 10(-4)mol L(-1) with the detection limit of 68 nM. Further experiments revealed that the modified electrode can be successfully applied for the accurate determination of Aza in pharmaceutical preparations.

  15. Differential Pulse Anodic Stripping Voltammetry for Mercury Determination

    Directory of Open Access Journals (Sweden)

    Vereștiuc Paul C.

    2015-07-01

    Full Text Available In the present work voltammetric investigations have been performed on HgCl2 aqueous solutions prepared from a Cz 9024 reagent. Carbon paste electrode (CPE, eriochrome black T modified carbon paste electrode (MCPE/EBT and KCl 1M as background electrolyte, were involved within the experimental procedures. Cyclic voltammetry (CV has been performed in order to compare the behaviour of the two electrodes in both K3[Fe(CN6] and mercury calibration aqueous solution. Differential pulse anodic stripping voltammetry (DPASV was used to determine the most suitable parameters for mercury determination. All experiments were performed at 25 ± 1 ℃, using an electrochemical cell with three-electrodes connected to an Autolab PG STAT 302N (Metrohm-Autolab potentiostat that is equipped with Nova 1.11 software. The measured potential values were generated by using the silver chloride electrode (AgClE as reference and a platinum wire electrode as auxiliary. A series of time depending equations for the pre-concentration and concentration steps were established, with the observation that a higher sensitivity can be obtained while increasing the pre-concentration time. DPASV were drawn using the CPE in 11.16 % coriander, as mercury complex, the voltamograms signals indicating mercury oxidation, with signal intensity increasing in time.

  16. Microtube strip heat exchanger

    Science.gov (United States)

    Doty, F. D.

    1991-04-01

    During the last quarter, Doty Scientific, Inc. (DSI) continued to make progress on the microtube strip (MTS) heat exchangers. The team has begun a heat exchanger stress analysis; however, they have been concentrating the bulk of their analytical energies on a computational fluid dynmaics (CFD) model to determine the location and magnitude of shell-side flow maldistribution which decreases heat exchanger effectiveness. DSI received 120 fineblanked tubestrips from Southern Fineblanking (SFB) for manufacturing process development. Both SFB and NIST provided inspection reports of the tubestrips. DSI completed the tooling required to encapsulate a tube array and press tubestrips on the array. Pressing the tubestrips on tube arrays showed design deficiencies both in the tubestrip design and the tooling design. DSI has a number of revisions in process to correct these deficiencies. The research effort has identified a more economical fusible alloy for encapsulating the tube array, and determined the parameters required to successfully encapsulate the tube array with the new alloy. A more compact MTS heat exchanger bank was designed.

  17. Nanocomposite electrodes made of carbon nanofibers and black wax. Anodic stripping voltammetry of zinc and lead.

    Science.gov (United States)

    van Dijk, N; Fletcher, S; Madden, C E; Marken, F

    2001-11-01

    Nanocomposite electrodes offer exciting new possibilities in electroanalytical chemistry. In this preliminary study, nanocomposite electrodes made of carbon nanofibers and black wax were characterized and investigated as novel substrates for metal deposition and stripping processes. Carbon nanofibers were grown from ethylene-hydrogen gas mixtures over Fe-Ni-Cu (85:10:5) nanoparticle catalysts at 600 degrees C and then embedded in Apiezon black wax under vacuum at 140 degrees C. The resulting nanocomposite electrodes showed (i) good conductivity, (ii) a wide potential window in aqueous solutions, (iii) low background currents, (iv) near steady state voltammetric responses with substantial Faradaic currents and (v) sharply peaked fast scan metal stripping responses. Zinc is a notoriously difficult metal to determine in aqueous solutions, because its deposition and stripping are accompanied by hydrogen evolution at extreme negative potentials. It therefore provided a challenging test for our new nanocomposite electrode. Although numerous complications associated with the hydrogen evolution process could not be eliminated, remarkably clear voltammograms could be obtained even at scan rates of 40 V s(-1).

  18. Magnetic stripping studies for SPL

    CERN Document Server

    Posocco, P; CERN. Geneva. BE Department

    2010-01-01

    Magnetic stripping of H- can seriously enhance the beam losses along the SPL machine. These losses depend on the beam energy, on the beam transverse distribution and on the intensity of the magnetic field. For radioprotection issues the losses must be limited to 1 W/m. In this paper we will concentrate on the stripping phenomena inside the quadrupole magnets with the aim of defining the quadrupole range for the design phase of SPL.

  19. Improved lower bound for online strip packing

    NARCIS (Netherlands)

    Harren, Rolf; Kern, Walter

    2012-01-01

    In the two-dimensional strip packing problem a number of rectangles have to be packed without rotation or overlap into a strip such that the height of the strip used is minimal. The width of the rectangles is bounded by 1 and the strip has width 1 and infinite height. We study the online version of

  20. The Dark Side of the Moebius Strip.

    Science.gov (United States)

    Schwarz, Gideon E.

    1990-01-01

    Discussed are various models proposed for the Moebius strip. Included are a discussion of a smooth flat model and two smooth flat algebraic models, some results concerning the shortest Moebius strip, the Moebius strip of least elastic energy, and some observations on real-world Moebius strips. (KR)

  1. Thick-film voltammetric pH-sensors with internal indicator and reference species

    DEFF Research Database (Denmark)

    Musa, Arnaud Emmanuel; Alonso-Lomillo, María Asunción; del Campo, Francisco Javier

    2012-01-01

    The following paper describes the development of a screen-printed voltammetric pH-sensor based on graphite electrodes incorporating both internal indicator (i.e., phenanthraquinone) and reference species (i.e., dimethylferrocene). The key advantages of this type of system stem from its simplicity......, low cost and ease of fabrication. More importantly, as opposed to conventional voltammetric systems where the height of the voltammetric peaks is taken into account to quantify the amount of a species of interest, here, the difference between the peak potential of the indicator species and the peak...... potential of the reference species is used. Thus, this measurement principle makes the electrochemical system presented here less dependent on the potential of the reference electrode (RE), as is often the case in other electrochemical systems. The developed system displays very promising performances...

  2. Cathodic stripping voltammetry of trace Mn(II) at carbon film electrodes.

    Science.gov (United States)

    Filipe, Olga M S; Brett, Christopher M A

    2003-12-04

    A sensitive voltammetric method is presented for the determination of tract levels of Mn (II) using carbon film electrodes fabricated from carbon resistors of 2 Omega. Determination of manganese was made by square wave cathodic stripping voltammetry (CSV), with deposition of manganese as manganese dioxide. Chronoamperometric experiments were made to study MnO(2) nucleation and growth. As a result, it was found to be necessary to perform electrode conditioning at a more positive potential to initiate MnO(2) nucleation. Under optimised conditions the detection limit obtained was 4 nM and the relative standard deviation for eight measurements of 0.22 nM was 5.3%. Interferences from various metal ions on the response CSV of Mn(II) were investigated, namely Cd(II), Ni(II), Cu(II), Cr(VI), Pb(II), Zn(II) and Fe(II). Application to environmental samples was demonstrated.

  3. Lead migration from toys by anodic stripping voltammetry using a bismuth film electrode.

    Science.gov (United States)

    Leal, M Fernanda C; Catarino, Rita I L; Pimenta, Adriana M; Souto, M Renata S; Afonso, Christelle S; Fernandes, Ana F Q

    2016-09-02

    Metals may be released from toys via saliva during mouthing, via sweat during dermal contact, or via gastric and intestinal fluids after partial or whole ingestion. In this study, we determined the lead migration from toys bought on the Portuguese market for children below 3 years of age. The lead migration was performed according to the European Committee for Standardization EN 71-3, which proposes a 2-hour migration test that simulates human gastric conditions. The voltammetric determination of migrated lead was performed by anodic stripping voltammetry (ASV) at a bismuth film electrode (BiFE). For all the analyzed toys, the values of migrated lead did not exceed the limits imposed by the European Committee for Standardization EN 71-3 (90 mg kg(-1)) and by the EU Directive 2009/48/EC (13.5 mg kg(-1)) on the safety of toys.

  4. Inorganic arsenic speciation by differential pulse anodic stripping voltammetry using thoria nanoparticles-carbon paste electrodes.

    Science.gov (United States)

    Pereira, F J; Vázquez, M D; Debán, L; Aller, A J

    2016-05-15

    Two novel thoria (ThO2) nanoparticles-carbon paste electrodes were used to evaluate an anodic stripping voltammetric method for the direct determination of arsenite and total inorganic arsenic (arsenite plus arsenate) in water samples. The effect of Ag((I)), Cu((II)), Hg((II)), Sb((III)) and Se((IV)) ions on the electrochemical response of arsenic was assayed. The developed electroanalytical method offers a rapid procedure with improved analytical characteristics including good repeatability (3.4%) at low As((III)) concentrations, high selectivity, lower detection limit (0.1 μg L(-1)) and high sensitivity (0.54 μA μg(-1) L). The analytical capability of the optimized method was demonstrated by the determination of arsenic in certified reference materials (trace elements in natural water, trace elements in water and coal fly ash).

  5. Avaliação da influência de sulfetos solúveis na complexação do cobre em águas superficiais empregando métodos voltamétricos Influence of dissolved sulfides on copper complexation in surface waters using voltammetric methods

    Directory of Open Access Journals (Sweden)

    Elizabeth W. O. Scheffer

    2010-01-01

    Full Text Available In this work a sulfide quantification protocol using voltammetric methods was developed to evaluate the effect of dissolved sulfides on copper complexation. On the basis of pH, sulfide release from the dissociation of specific metal sulfide complexes can be electrochemically measured and then removed (as H2S by a N2 purge. Cathodic stripping square wave voltammetry (CSSWV was conducted to quantify Cu sulfides complexes which dissociate at pH < 5.0 during the process of acid titration.

  6. Especiação analítica de compostos de arsênio empregando métodos voltamétricos e polarográficos: uma revisão comparativa de suas principais vantagens e aplicações Speciation analysis of arsenic compounds by voltammetric and polarographic methods: a comparative review of their main advantages and applications

    Directory of Open Access Journals (Sweden)

    Leandro Machado de Carvalho

    2004-04-01

    Full Text Available This paper provides a review on voltammetric and polarographic methods for the speciation analysis of inorganic and organic arsenic compounds in different matrices. A discussion on the main advantages of electroanalytical methods in comparison with other analytical methods employed for arsenic speciation is presented. The mechanistic aspects of the most relevant techniques employing cathodic and anodic stripping voltammetry as well as polarographic methods published in the last twenty five years are summarized and discussed. The bibliographic references cited in this work were selected from the Web of Science (published by the ISI and the main journals of analytical chemistry.

  7. Discrimination of Rice with Different Pretreatment Methods by Using a Voltammetric Electronic Tongue

    Directory of Open Access Journals (Sweden)

    Li Wang

    2015-07-01

    Full Text Available In this study, an application of a voltammetric electronic tongue for discrimination and prediction of different varieties of rice was investigated. Different pretreatment methods were selected, which were subsequently used for the discrimination of different varieties of rice and prediction of unknown rice samples. To this aim, a voltammetric array of sensors based on metallic electrodes was used as the sensing part. The different samples were analyzed by cyclic voltammetry with two sample-pretreatment methods. Discriminant Factorial Analysis was used to visualize the different categories of rice samples; however, radial basis function (RBF artificial neural network with leave-one-out cross-validation method was employed for prediction modeling. The collected signal data were first compressed employing fast Fourier transform (FFT and then significant features were extracted from the voltammetric signals. The experimental results indicated that the sample solutions obtained by the non-crushed pretreatment method could efficiently meet the effect of discrimination and recognition. The satisfactory prediction results of voltammetric electronic tongue based on RBF artificial neural network were obtained with less than five-fold dilution of the sample solution. The main objective of this study was to develop primary research on the application of an electronic tongue system for the discrimination and prediction of solid foods and provide an objective assessment tool for the food industry.

  8. Discrimination of Rice with Different Pretreatment Methods by Using a Voltammetric Electronic Tongue.

    Science.gov (United States)

    Wang, Li; Niu, Qunfeng; Hui, Yanbo; Jin, Huali

    2015-07-22

    In this study, an application of a voltammetric electronic tongue for discrimination and prediction of different varieties of rice was investigated. Different pretreatment methods were selected, which were subsequently used for the discrimination of different varieties of rice and prediction of unknown rice samples. To this aim, a voltammetric array of sensors based on metallic electrodes was used as the sensing part. The different samples were analyzed by cyclic voltammetry with two sample-pretreatment methods. Discriminant Factorial Analysis was used to visualize the different categories of rice samples; however, radial basis function (RBF) artificial neural network with leave-one-out cross-validation method was employed for prediction modeling. The collected signal data were first compressed employing fast Fourier transform (FFT) and then significant features were extracted from the voltammetric signals. The experimental results indicated that the sample solutions obtained by the non-crushed pretreatment method could efficiently meet the effect of discrimination and recognition. The satisfactory prediction results of voltammetric electronic tongue based on RBF artificial neural network were obtained with less than five-fold dilution of the sample solution. The main objective of this study was to develop primary research on the application of an electronic tongue system for the discrimination and prediction of solid foods and provide an objective assessment tool for the food industry.

  9. Development of a rapid and simple voltammetric method to determine total antioxidative capacity of edible oils.

    Science.gov (United States)

    Gulaboski, Rubin; Mirčeski, Valentin; Mitrev, Saša

    2013-05-01

    In this work we report on a new, rapid and simple voltammetric method to determine the total antioxidant capacity (TAC) of the edible oils. The method explores the ABTS radical (2,2'-azinobis(3-ethylbenzothiazoline-6-sulphonic acid)) assay as a redox probe and it relays on measuring catalytic voltammetric currents. The electrocatalysis comprises redox regeneration of the electrochemically created ABTS(+) radical either by Trolox (6-hydroxy-2,5,7,8-tetramethychroman-2-carboxylic acid) or by antioxidants present in studied oils. The detection limit of the method is determined to be 0.5 mg/L of Trolox equivalent, being a slightly lower than the corresponding UV-VIS spectrophotometric method. Applying the proposed voltammetric method the total antioxidant capacity of three types of commercially available cold-pressed edible oils are determined, and the results are found to be in a very good agreement with those obtained by UV-VIS spectrophotometry. The reported voltammetric method is cheap, rapid and simple, and it can be used as a sustainable alternative to the UV-VIS methods for the determination of total antioxidant capacitance of oils and other liquid lipophilic nutrients. Potent antioxidant capacity of studied oils was also confirmed by electron paramagnetic resonance spectroscopy of superoxide anion produced by macrophages.

  10. VOLTAMMETRIC BEHAVIOR OF SOME STEELS IN AQUEOUS SOLUTIONS OF HNO3

    Directory of Open Access Journals (Sweden)

    Gheorghe Nemtoi

    2011-06-01

    Full Text Available The corrosion process of some steels immersed in HNO3 solutions of different concentrations by means of voltammetric measurements was investigated. For different values of the corrosion potential, or of the contact time: solid steel-aggressive medium, several equations of the type: I = f (E were proposed, only for linear domains of the voltammograms.

  11. Restitution of enamel after interdental stripping.

    Science.gov (United States)

    Lundgren, T; Milleding, P; Mohlin, B; Nannmark, U

    1993-01-01

    This paper studies the effect of interdental stripping on the enamel surface and evaluates methods to restitute the treated surface. Extracted teeth mounted in a semielastic material were subjected to stripping by different kinds of steel strips. The treated enamel surfaces were then polished in several different ways. The effects were studied by SEM and profilometry. It was concluded that the coarsest strips produced irregularities of such a magnitude that polishing had very limited effect. Polishing starting with coarse polishing strips followed by gradually finer gave the best result. An increase in number of strokes and use of all grades of polishing strips slightly improved the result.

  12. Modified electrode voltammetric sensors for trace metals in environmental samples

    Directory of Open Access Journals (Sweden)

    Brett Christopher M.A.

    2000-01-01

    Full Text Available Nafion-modified mercury thin film electrodes have been investigated for the analysis of trace metals in environmental samples of waters and effluent by batch injection analysis with square wave anodic stripping voltammetry. The method, involving injection over the detector electrode of untreated samples of volume of the order of 50 microlitres has fast response, blocking and fouling of the electrode is minimum as shown by studies with surface-active components. Comparison is made between glassy carbon substrate electrodes and carbon fibre microelectrode array substrates, the latter leading to a small sensitivity enhancement. Application to analysis of river water and industrial effluent for labile zinc, cadmium, lead and copper ions is demonstrated in collected samples and after acid digestion.

  13. The voltammetric responses of nanometer-sized electrodes in weakly supported electrolyte: A theoretical study

    Energy Technology Data Exchange (ETDEWEB)

    Liu Yuwen; Zhang Qianfan [Hubei Electrochemical Power Sources Key Laboratory, Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072 (China); Chen Shengli, E-mail: slchen@whu.edu.c [Hubei Electrochemical Power Sources Key Laboratory, Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072 (China)

    2010-11-30

    The effect of the supporting electrolyte concentration on the interfacial profiles and voltammetric responses of nanometer-sized disk electrodes have been investigated theoretically by combining the Poisson-Nernst-Planck (PNP) theory and Butler-Volmer (BV) equation. The PNP-theory is used to treat the nonlinear couplings of electric field, concentration field and dielectric field at electrochemical interface without the electroneutrality assumption that has been long adopted in various voltammetric theories for macro/microelectrodes. The BV equation is modified by using the Frumkin correction to account for the effect of the diffuse double layer potential on interfacial electron-transfer (ET) rate and by including a distance-dependent ET probability in the expression of rate constant to describe the radial heterogeneity of the ET rate constant at nanometer-sized disk electrodes. The computed voltammetric responses for disk electrodes larger than 200 nm in radii in the absence of the excess of the supporting electrolyte using the present theoretical scheme show reasonable agreements with the predications of the conventional microelectrode voltammetric theory which uses the combined Nernst-Planck equation and electroneutrality equation to describe the mixed electromigration-diffusion mass transport without including the possible effects of the diffuse double layer (Amatore et al. ). For electrodes smaller than 200 nm, however, the voltammetric responses predicated by the present theory exhibit significant deviation from the microelectrode theory. It is shown that the deviations are mainly resulted from the overlap between the diffuse double layer and the concentration depletion layer (CDL) at nanoscale electrochemical interfaces in weakly supported media, which will result in the invalidation of the electroneutrality condition in CDL, and from the radial inhomogeneity of ET probability at nanometer-sized disk electrodes.

  14. Hardy spaces for the strip

    Science.gov (United States)

    Bakan, Andrew; Kaijser, Sten

    2007-09-01

    In this paper we shall study Hardy spaces of analytic functions in a strip . Our main result is on one hand an intrinsic characterization of the spaces and on the second that polynomials are dense. We also present an orthogonal (in ) basis of polynomials.

  15. Adsorption Rate Models for Multicomponent Adsorption Systems

    Institute of Scientific and Technical Information of China (English)

    姚春才

    2004-01-01

    Three adsorption rate models are derived for multicomponent adsorption systems under either pore diffusion or surface diffusion control. The linear driving force (LDF) model is obtained by assuming a parabolic intraparticle concentration profile. Models I and Ⅱ are obtained from the parabolic concentration layer approximation. Examples are presented to demonstrate the usage and accuracy of these models. It is shown that Model I is suitable for batch adsorption calculations and Model Ⅱ provides a good approximation in fixed-bed adsorption processes while the LDF model should not be used in batch adsorption and may be considered acceptable in fixed-bed adsorption where the parameter Ti is relatively large.

  16. Intraply Hybrid Composites Would Contain Control Strips

    Science.gov (United States)

    Chamis, Christos C.; Shiao, Chi-Yu

    1996-01-01

    "Smart" structural components with sensors and/or actuators distributed throughout their volumes made of intraply hybrid composite materials, according to proposal. Strips of hybrid control material interspersed with strips of ordinary (passive) composite material in some layers, providing distributed control capability. For example, near and far edges of plate bent upward by commanding bottom control strips to expand and simultaneously commanding upper control strips to contract.

  17. Adsorption and wetting.

    NARCIS (Netherlands)

    Schlangen, L.J.M.

    1995-01-01

    Adsorption and wetting are related phenomena. In order to improve knowledge of both and their relations, experiments, thermodynamics and a theoretical interpretation have been connected, starring n-alkanes.Starting from the Gibbs adsorption equation thermodynamic relations between vapour adsorption

  18. Using Comic Strips in Language Classes

    Science.gov (United States)

    Csabay, Noémi

    2006-01-01

    The author believes that using comic strips in language-learning classes has three main benefits. First, comic strips motivate younger learners. Second, they provide a context and logically connected sentences to help language learning. Third, their visual information is helpful for comprehension. The author argues that comic strips can be used in…

  19. Voltammetric studies of Azathioprine on the surface of graphite electrode modified with graphene nanosheets decorated with Ag nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Asadian, Elham [Institute for Nanoscience and Nanotechnology (INST), Sharif University of Technology, Tehran (Iran, Islamic Republic of); Iraji zad, Azam [Institute for Nanoscience and Nanotechnology (INST), Sharif University of Technology, Tehran (Iran, Islamic Republic of); Department of Physics, Sharif University of Technology, Tehran 14588-89694 (Iran, Islamic Republic of); Shahrokhian, Saeed, E-mail: shahrokhian@sharif.edu [Institute for Nanoscience and Nanotechnology (INST), Sharif University of Technology, Tehran (Iran, Islamic Republic of); Department of Chemistry, Sharif University of Technology, Tehran 11155-9516 (Iran, Islamic Republic of)

    2016-01-01

    By using graphene nanosheets decorated with Ag nanoparticles (AgNPs-G) as an effective approach for the surface modification of pyrolytic graphite electrode (PGE), a sensing platform was fabricated for the sensitive voltammetric determination of Azathioprine (Aza). The prepared AgNPs-G nanosheets were characterized using transmission electron microscopy (TEM), X-ray diffraction (XRD), UV–vis and Raman spectroscopy techniques. The electrochemical behavior of Aza was investigated by means of cyclic voltammetry. Comparing to the bare PGE, a remarkable enhancement was observed in the response characteristics of Aza on the surface of the modified electrode (AgNPs-G/PGE) as well as a noticeable decrease in its reduction overpotential. These results can be attributed to the incredible enlargement in the microscopic surface area of the electrode due to the presence of graphene nanosheets together with strong adsorption of Aza on its surface. The effect of experimental parameters such as accumulation time, the amount of modifier suspension and pH of the supporting electrolyte were also optimized toward obtaining the maximum sensitivity. Under the optimum conditions, the calibration curve studies demonstrated that the peak current increased linearly with Aza concentrations in the range of 7 × 10{sup −7} to 1 × 10{sup −4} mol L{sup −1} with the detection limit of 68 nM. Further experiments revealed that the modified electrode can be successfully applied for the accurate determination of Aza in pharmaceutical preparations. - Highlights: • A novel electrochemical sensing platform based on graphene nanosheets decorated with Ag nanoparticles was constructed for determination of Azathioprine. • The prepared modified electrode showed an efficient catalytic role toward the electro-reduction of Azathioprine. • The prepared modified electrode shows a wide linear dynamic range and a nanomolar detection limit for Azathioprine. • The modification procedure provides a

  20. Cheap in situ voltammetric copper determination from freshwater samples

    Directory of Open Access Journals (Sweden)

    David I. G.

    2013-04-01

    Full Text Available Detection of low concentrations of heavy metals in environmental samples is of particular interest because most of them represent persistent, highly toxic pollutants. Cu2+ detection in environmental samples is important because it is typical heavy metal, being an essential element for human beings but at higher concentrations it can create health risks. Due to the accumulation steps involved, anodic stripping voltammetry (ASV is one of the most sensitive techniques used for the detection of low concentrations of metal ions form different environmental samples. In order to minimize sample loss during sample collection, storage and transportation it is of particular interest to perform in situ rapid and reliable routine analysis. In the present paper we describe the use of a simple, disposable pencil graphite electrode (PGE for the determination of Cu from river water samples by mercury film anodic stripping voltammetry. The investigated water samples were collected during a period of 3 years (2009-2011, from six sampling points situated along the lower part of the Prut River (Romania. ASV measurements were performed in the presence of Hg2+ in 0.1 M HNO3 at a carbon pencil graphite working electrode. Standard addition method was applied for the quantification of Cu2+. The Cu2+ content of the most river water samples analysed exceeded 2 ⎧g/L (MEWM, 2006, the maximum admitted concentration for surface waters, and these could be due to the anthropogenic activities in the region (e.g. the largest steel factory in Romania is located in the vicinity of the sampling area. Samples show an additional importance as the region is included in a protected area, Lower Prut Floodplain Natural Park, and trace elements transfer along the aquatic food chain has been previously documented (Matache et. al, 2012. The results obtained by ASV on PGE agreed well with those obtained by inductively coupled plasma atomic emission spectrometry (ICP-AES using the Romanian

  1. Metrological characteristics of the flat voltammetric electrode in time domain with a reversible electrochemical reaction running on the surface

    Science.gov (United States)

    Suchocki, Krzysztof

    2016-11-01

    The study deals with metrological characteristics of the flat voltammetric electrode used for determination of ions concentration by the DC voltammetric method, where a reversible reaction of electrochemical oxidation/reduction takes place on the surface. The analysis shows that such voltammetric electrode acts as a transducer of the first order, where the input signal is a concentration of marked ions in tested solution and the output signal is the current associated with a reversible reaction of oxidation / reduction. Metrological characteristics of such electrode in the time domain are determined by its sensitivity and time constant. The values of these parameters are defined by measurements of characteristics of the voltammetric electrode, polarization voltage and marked ions. To determine the effect of a particular volume of each of these parameters several numerical simulations are presented.

  2. Simple and rapid determination of trace iodide by cathodic stripping voltammetry.

    Science.gov (United States)

    Yang, Lingxi; Zou, Lina; Li, Gaiping; Ye, Baoxian

    2016-01-15

    This work establishes a highly sensitive and simple stripping voltammetric method for the direct determination of trace iodide. In the presence of abounding bromide and appropriate amount of cetylpyridine bromide (CPB), the iodine was accumulated on the glassy carbon electrode surface as ion association complex (CPBI2Br). After accumulation for a period of time, a linear sweep potential with negative scanning was applied and the I2 in CPBI2Br was reduced again into the solution. Under the optimization conditions, the stripping signals (peak current) were linear relationship with iodide concentration in range of 3.81×10(-3)µg/mL to 0.114 μg/mL and 0.127μg/mL to 2.54μg/mL, with a detection limit of 1.02ng/mL (S/N=3) for a accumulation time of 180s. Determination of trace iodine in pharmaceutical sample, kelp and table salt were performed with high accuracy and satisfactory recovery results. Copyright © 2015 Elsevier B.V. All rights reserved.

  3. Determination of Norfloxacin by square-wave adsorptive voltammetry on a glassy carbon electrode.

    Science.gov (United States)

    Ghoneim, M M; Radi, A; Beltagi, A M

    2001-05-01

    The adsorptive and electrochemical behavior of norfloxacin on a glassy carbon electrode were investigated by cyclic and square-wave voltammetry. Cyclic voltammetric studies indicated that the process was irreversible and fundamentally controlled by adsorption. To obtain a good sensitivity, the solution conditions and instrumental parameters were studied using square-wave voltammetry. In acetate buffer of pH 5.0, norfloxacin gave a sensitive adsorptive oxidative peak at 0.920 V (versus Ag-AgCl). Applicability to measurement of norfloxacin at submicromolar levels in urine samples was illustrated. The peak current was linear with the norfloxacin concentration in the range 5-50 microg ml(-1) urine. The detection limit was 1.1 microg ml(-1) urine.

  4. Simultaneous voltammetric determination of paracetamol and ascorbic acid using a boron-doped diamond electrode modified with Nafion and lead films.

    Science.gov (United States)

    Tyszczuk-Rotko, Katarzyna; Bęczkowska, Ilona; Wójciak-Kosior, Magdalena; Sowa, Ireneusz

    2014-11-01

    The paper describes the fabrication and application of a novel sensor (a boron-doped diamond electrode modified with Nafion and lead films) for the simultaneous determination of paracetamol and ascorbic acid by differential pulse voltammetry. The main advantage of the lead film and polymer covered boron-doped diamond electrode is that the sensitivity of the stripping responses is increased and the separation of paracetamol and ascorbic acid signals is improved due to the modification of the boron-doped diamond surface by the lead layer. Additionally, the repeatability of paracetamol and ascorbic acid signals is improved by the application of the Nafion film coating. In the presence of oxygen, linear calibration curves were obtained in a wide concentration range from 5×10(-7) to 2×10(-4) mol L(-1) for paracetamol and from 1×10(-6) to 5×10(-4) mol L(-1) for ascorbic acid. The analytical utility of the differential pulse voltammetric method elaborated was tested in the assay of paracetamol and ascorbic acid in commercially available pharmaceutical formulations and the method was validated by high performance liquid chromatography coupled with diode array detector.

  5. Ion-transfer voltammetric determination of the beta-blocker propranolol in a physiological matrix at silicon membrane-based liquid|liquid microinterface arrays.

    Science.gov (United States)

    Collins, Courtney J; Arrigan, Damien W M

    2009-03-15

    In this work, the ion-transfer voltammetric detection of the protonated beta-blocker propranolol in artificial saliva is presented. Cyclic voltammetry, differential pulse voltammetry, and differential pulse stripping voltammetry (DPSV) were employed in the detection of the cationic drug based on ion-transfer voltammetry across arrays of microinterfaces between artificial saliva and an organogel phase. It was found that the artificial saliva matrix decreased the available potential window for ion-transfer voltammetry at this liquid|liquid interface but transfer of protonated propranolol was still achieved. The DPSV method employed a preconditioning step as well as a preconcentration step followed by analytical signal generation based on the back-transfer of the drug across the array of microinterfaces. The DPSV peak current response was linear with drug concentration in the artificial saliva matrix over the concentration range of 0.05-1 microM (i(p) = -8.13 (nA microM(-1))(concentration) + 0.07 (nA), R = 0.9929, n = 7), and the calculated detection limit (3s(b)) was 0.02 microM. These results demonstrate that DPSV at arrays of liquid|liquid microinterfaces is a viable analytical approach for pharmaceutical determinations in biomimetic matrixes.

  6. Voltammetric determination of Se(IV) and Se(VI) in saline samples-Studies with seawater, hydrothermal and hemodialysis fluids

    Energy Technology Data Exchange (ETDEWEB)

    Nascimento, Paulo C. do, E-mail: npaulo@quimica.ufsm.br [Departamento de Quimica, Universidade Federal de Santa Maria, C.P. 5051, 97105-970 Santa Maria, RS (Brazil); Jost, Cristiane L.; Carvalho, Leandro M. de; Bohrer, Denise [Departamento de Quimica, Universidade Federal de Santa Maria, C.P. 5051, 97105-970 Santa Maria, RS (Brazil); Koschinsky, Andrea [School of Engineering and Science, Geosciences and Astrophysics, Jacobs University Bremen GmbH, P.O. Box 750561, D-28725 Bremen (Germany)

    2009-08-26

    Determination of Se(IV) and Se(VI) in high saline media was investigated by cathodic stripping voltammetry (CSV). The voltammetric method was applied to assay selenium in seawater, hydrothermal and hemodialysis fluids. The influence of ionic strength on selenium determination is discussed. The CSV method was based on the co-electrodeposition of Se(IV) with Cu(II) ions and Se(VI) determined by difference after sample UV-irradiation for photolytic selenium reduction. UV-irradiation was also used as sample pre-treatment for organic matter decomposition. Detection limit of 0.030 {mu}g L{sup -1} (240 s deposition time) and relative standard deviation (RSD) of 6.19% (n = 5) for 5.0 {mu}g L{sup -1} of Se(IV) were calculated. Linear calibration range for selenium was observed from 1.0 to 100.0 {mu}g L{sup -1}. Concerning the pre-treatment step, best results were obtained by using 60 min UV-irradiation interval in H{sub 2}O{sub 2}/HCl medium. Se(VI) was reduced to the Se(IV) electroactive species with recoveries between 91.7% and 112.9%. Interferents were also investigated.

  7. Fast variation method for elastic strip calculation.

    Science.gov (United States)

    Biryukov, Sergey V

    2002-05-01

    A new, fast, variation method (FVM) for determining an elastic strip response to stresses arbitrarily distributed on the flat side of the strip is proposed. The remaining surface of the strip may have an arbitrary form, and it is free of stresses. The FVM, as well as the well-known finite element method (FEM), starts with the variational principle. However, it does not use the meshing of the strip. A comparison of FVM results with the exact analytical solution in the special case of shear stresses and a rectangular strip demonstrates an excellent agreement.

  8. The Voltammetric Analysis of Selenium Electrodeposition from H2SeO3 Solution on Gold Electrode

    Directory of Open Access Journals (Sweden)

    Kowalik R.

    2015-04-01

    Full Text Available The different voltammetry techniques were applied to understand the process of selenium deposition from sulfate solution on gold polycrystalline electrode. By applying the cycling voltammetry with different scan limits as well as the chronoamper-ometry combined with the cathodic and anodic linear stripping voltammetry, the different stages of the deposition of selenium were revealed. It was found that the process of reduction of selenous acid on gold surface exhibits a multistage character. The cyclic voltammetry results showed four cathodic peaks which are related to the surface limited phenomena and which coincide with the bulk deposition process. The fifth cathodic peak is related to the reduction of bulk deposited Se0 to Se-2 ions. Furthermore, the connection of anodic peaks with cathodic ones confirmed the surface limited process of selenium deposition, bulk deposition and reduction to Se-2. Additionally, the cathodic linear stripping voltammetry confirms the process of H2SeO3 adsorption on gold surface. The experiments confirmed that classical voltammetry technique proved to be a very powerful tool for analyzing the electrochemical processes related with interfacial phenomena and electrodeposition.

  9. Antenna structure with distributed strip

    Science.gov (United States)

    Rodenbeck, Christopher T.

    2008-03-18

    An antenna comprises electrical conductors arranged to form a radiating element including a folded line configuration and a distributed strip configuration, where the radiating element is in proximity to a ground conductor. The folded line and the distributed strip can be electrically interconnected and substantially coplanar. The ground conductor can be spaced from, and coplanar to, the radiating element, or can alternatively lie in a plane set at an angle to the radiating element. Embodiments of the antenna include conductor patterns formed on a printed wiring board, having a ground plane, spacedly adjacent to and coplanar with the radiating element. Other embodiments of the antenna comprise a ground plane and radiating element on opposed sides of a printed wiring board. Other embodiments of the antenna comprise conductors that can be arranged as free standing "foils". Other embodiments include antennas that are encapsulated into a package containing the antenna.

  10. Application of anodic stripping voltammetry for zinc, copper, and cadmium quantification in the aqueous humor: implications of pseudoexfoliation syndrome.

    Science.gov (United States)

    Panteli, Vassiliki S; Kanellopoulou, Dimitra G; Gartaganis, Sotirios P; Koutsoukos, Petros G

    2009-12-01

    Anodic stripping voltammetric (ASV) procedure, using mercury film electrode, was optimized and applied to determine the concentrations of zinc, cadmium, and copper in the aqueous humor. Concentration levels as low as 1 ppb of the test metals was possible to be detected using short electrolysis times (120 s) and microquantities of aqueous humor (up to 35 μL). As a first application of the voltammetric analysis of trace metals in the aqueous humor, the role of the three selected trace elements in the pseudoexfoliation (PEX) syndrome was examined. Samples from aqueous humor were collected during cataract extraction from patients with and without PEX. The zinc and copper concentration levels in the aqueous humor did not show statistically significant difference in the study and control group. Cadmium was detected in a small number of samples, without however statistical differences between the two groups. ASV proved to be a highly precise and sensitive tool for the quantification of heavy metal ions in aqueous humor. Further studies may lead to useful conclusions for the role of zinc, copper, or cadmium in PEX syndrome.

  11. Thermodynamic analysis of (bi)sulphate adsorption on a Pt(1 1 1) electrode as a function of pH

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Araez, Nuria; Climent, Victor; Rodriguez, Paramaconi; Feliu, Juan M. [Instituto de Electroquimica, Universidad de Alicante, Apt. 99, E-03080 Alicante (Spain)

    2008-10-01

    A complete thermodynamic study of (bi)sulphate adsorption on Pt(1 1 1) electrodes from solutions at four different pHs (pH 0.43, 2.1, 3.1 and 4.1) is reported. The effect of pH on the sum of the Gibbs excesses of sulphate and bisulphate species, standard Gibbs energies of adsorption and formal partial charge numbers is analyzed. The results provide relevant information on the nature of species involved in the different voltammetric features. The experiments at pH 0.43 were performed in a higher base electrolyte concentration (0.5 M), that allows the study of (bi)sulphate adsorption in a broader range of concentrations. Under these conditions, two adsorption steps are clearly defined, associated to two different voltammetric features, between 0.30 and 0.60 V and between 0.65 and 0.90 V (standard hydrogen scale, SHE). Once the pH is increased, a marked decrease in absolute value of the (bi)sulphate adsorption Gibbs energy is observed, concomitant with an increasing amount of OH co-adsorption. (author)

  12. A rapid cyclic voltammetric method for studying cement factors affecting the corrosion of reinforced concrete

    Energy Technology Data Exchange (ETDEWEB)

    Foulkes, F.R.; McGrath, P. (Univ. of Toronto, Ontario (Canada))

    1999-06-01

    A rapid cyclic voltammetric method for studying the influence of cement factors on the corrosion of embedded iron and steel in hardened cement paste is described. The technique employs a cement electrode'' consisting of an iron or steel wire embedded in a miniature cylinder of hardened cement paste. The rapid cyclic voltammetric method is fast, reproducible, and provides information on the corrosiveness of the pore solution environment surrounding the embedded metal. The usefulness of the method is demonstrated by showing how it can be used to evaluate the threshold chloride content of hardened ordinary portland cement paste at which corrosion begins and by using it to evaluate the relative efficacy of several admixed corrosion inhibitors.

  13. A zeolite modified carbon paste electrode as useful sensor for voltammetric determination of acetaminophen.

    Science.gov (United States)

    Ahmadpour-Mobarakeh, Leila; Nezamzadeh-Ejhieh, Alireza

    2015-04-01

    The voltammetric behavior of a carbon paste electrode modified with Co(II)-exchanged zeolite A (Co(II)-A/ZMCPE) for determination of acetaminophen was studied. The proposed electrode showed a diffusion controlled reaction with the electron transfer rate constant (Ks) of 0.44s(-1) and charge transfer coefficient of 0.73 in the absence of acetaminophen. A linear voltammetric response was obtained in the range of 0.1 to 190μmolL(-1) of acetaminophen [r(2)=0.9979, r=0.9989 (n=10)] with a detection limit of 0.04μmolL(-1). The method was successfully applied to the analysis of acetaminophen in some drugs.

  14. Differential pulse voltammetric determination of tin in the presence of noble metals

    Energy Technology Data Exchange (ETDEWEB)

    Monticelli, Damiano; Pozzi, Andrea; Dossi, Carlo; Recchia, Sandro [Universita degli Studi dell' Insubria, Dipartimento di Scienze Chimiche e Ambientali, Como (Italy); Psaro, Rinaldo [CNR Institute ' ' ISTM' ' , Milano (Italy)

    2005-09-01

    A voltammetric method for the determination of tin is proposed to minimise interferences from noble metals that are commonly encountered with other analytical techniques. Strong distortions of voltammetric peaks are observed in the presence of platinum. On the basis of a full investigation, the formation of an intermediate Sn(II)-Pt mixed chloro-complex at the electrode surface is identified as being responsible for the platinum interference, as it competes with the normal Sn(IV){yields}Sn(0){sub Hg} reduction. The use of a higher scan rate prevents the relatively low reaction kinetics and thus gets rid of this interference. No problems are encountered with other noble metals such as Pd, Ir, Re, Rh and Ru when using the modified method, although a baseline subtraction is necessary for the latter one. The proposed method is validated with real Pt-Sn catalysts. (orig.)

  15. Voltammetric Studies of the Interaction of Tris (1, 10-phenanthroline) Cobalt (Ⅲ) with Bovine Serum Albumin

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The voltammetric methods were used to prove the interaction of metal complex Co(phen)33+ with bovine serum albumin (BSA). The interaction of BSA with Co(phen)33+ molecules using BSA-modified electrode is described. Information of the binding ratio and interaction mode can be obtained from their electrochemical behavior and electrochemical data. Furthermore, attenuated total reflection infrared experiment was performed to prove the interaction between complexes and BSA.

  16. Mesoporous carbon-containing voltammetric biosensor for determination of tyramine in food products

    OpenAIRE

    Kochana, Jolanta; Wapiennik, Karolina; Knihnicki, Paweł; Pollap, Aleksandra; Janus, Paula; Oszajca, Marcin; Kuśtrowski, Piotr

    2016-01-01

    A voltammetric biosensor based on tyrosinase (TYR) was developed for determination of tyramine. Carbon material (multi-walled carbon nanotubes or mesoporous carbon CMK-3-type), polycationic polymer—i.e., poly(diallyldimethylammonium chloride) (PDDA), and Nafion were incorporated into titania dioxide sol (TiO2) to create an immobilization matrix. The features of the formed matrix were studied by scanning electron microscopy (SEM) and cyclic voltammetry (CV). The analytical performance of the d...

  17. A voltammetric and mathematical analysis of histaminergic modulation of serotonin in the mouse hypothalamus.

    Science.gov (United States)

    Samaranayake, Srimal; Abdalla, Aya; Robke, Rhiannon; Nijhout, H Frederik; Reed, Michael C; Best, Janet; Hashemi, Parastoo

    2016-08-01

    Histamine and serotonin are neuromodulators which facilitate numerous, diverse neurological functions. Being co-localized in many brain regions, these two neurotransmitters are thought to modulate one another's chemistry and are often implicated in the etiology of disease. Thus, it is desirable to interpret the in vivo chemistry underlying neurotransmission of these two molecules to better define their roles in health and disease. In this work, we describe a voltammetric approach to monitoring serotonin and histamine simultaneously in real time. Via electrical stimulation of the axonal bundles in the medial forebrain bundle, histamine release was evoked in the mouse premammillary nucleus. We found that histamine release was accompanied by a rapid, potent inhibition of serotonin in a concentration-dependent manner. We developed mathematical models to capture the experimental time courses of histamine and serotonin, which necessitated incorporation of an inhibitory receptor on serotonin neurons. We employed pharmacological experiments to verify that this serotonin inhibition was mediated by H3 receptors. Our novel approach provides fundamental mechanistic insights that can be used to examine the full extent of interconnectivity between histamine and serotonin in the brain. Histamine and serotonin are co-implicated in many of the brain's functions. In this paper, we develop a novel voltammetric method for simultaneous real-time monitoring of histamine and serotonin in the mouse premammillary nucleus. Electrical stimulation of the medial forebrain bundle evokes histamine and inhibits serotonin release. We show voltammetrically, mathematically, and pharmacologically that this serotonin inhibition is H3 receptor mediated.

  18. Voltammetric determination of Δ9-THC in glassy carbon electrode: An important contribution to forensic electroanalysis.

    Science.gov (United States)

    Balbino, Marco Antonio; de Menezes, Matheus Manoel Teles; Eleotério, Izabel Cristina; Saczk, Adelir Aparecida; Okumura, Leonardo Luiz; Tristão, Heloísa Maria; de Oliveira, Marcelo Firmino

    2012-09-10

    A new voltammetric method for the determination of Δ(9)-tetrahydrocannabinol (Δ(9)-THC) is described. The voltammetric experiments were accomplished in N-N dimethylformamide/water (9:1, v/v), using tetrabutylammonium tetrafluoroborate (TBATFB) 0.1mol/L as supporting electrolyte and a glassy carbon disk electrode as the working electrode. The anodic peak current was observed at 0.0V (vs. Ag/AgCl) after a 30s pre-concentration step under an applied potential of -1.2V (vs. Ag/AgCl). A linear dependence of Δ(9)-THC detection was obtained in the concentration range 2.4-11.3ng/mL, with a linear correlation coefficient of 0.999 and a detection limit of 0.34ng/mL. The voltammetric method was used to measure the content of Δ(9)-THC in samples (hemp and hashish) confiscated by the police. The elimination of chemical interferences from the samples was promptly achieved through prior purification using the TLC technique, by employing methanol/water (4:1, v/v) as the mobile phase. The results showed excellent correlation with results attained by HPLC.

  19. A zeolite modified carbon paste electrode as useful sensor for voltammetric determination of acetaminophen

    Energy Technology Data Exchange (ETDEWEB)

    Ahmadpour-Mobarakeh, Leila; Nezamzadeh-Ejhieh, Alireza, E-mail: arnezamzadeh@iaush.ac.ir

    2015-04-01

    The voltammetric behavior of a carbon paste electrode modified with Co(II)-exchanged zeolite A (Co(II)-A/ZMCPE) for determination of acetaminophen was studied. The proposed electrode showed a diffusion controlled reaction with the electron transfer rate constant (K{sub s}) of 0.44 s{sup −1} and charge transfer coefficient of 0.73 in the absence of acetaminophen. A linear voltammetric response was obtained in the range of 0.1 to 190 μmol L{sup −1} of acetaminophen [r{sup 2} = 0.9979, r = 0.9989 (n = 10)] with a detection limit of 0.04 μmol L{sup −1}. The method was successfully applied to the analysis of acetaminophen in some drugs. - Highlights: • Modified carbon paste electrode with Co(II)-zeolite A improved the voltammetric current in determination of acetaminophen. • Modified electrode is applicable for acetaminophen in real samples. • The proposed method has good reproducibility and repeatability.

  20. Buffer strips in composites at elevated temperature

    Science.gov (United States)

    Bigelow, C. A.

    1983-01-01

    The composite material 'buffer strip' concept is presently investigated at elevated temperatures for the case of graphite/polyimide buffer strip panels using a (45/0/45/90)2S layup, where the buffer strip material was 0-deg S-glass/polyimide. Each panel was loaded in tension until it failed, and radiographs and crack opening displacements were recorded during the tests to determine fracture onset, fracture arrest, and the extent of damage in the buffer strip after crack arrest. At 177 + or - 3 C, the buffer strips increased the panel strength by at least 40 percent in comparison with panels without buffer strips. Compared to similar panels tested at room temperature, those tested at elevated temperature had lower residual strengths, but higher failure strains.

  1. Stripping, Sex, and Popular Culture

    OpenAIRE

    Roach, Catherine M.

    2007-01-01

    At the heart of Stripping, Sex, and Popular Culture lies a very personal story, of author Catherine Roach's response to the decision of her life-long best friend to become an exotic dancer. Catherine and Marie grew up together in Canada and moved to the USA to enroll in PhD programs at prestigious universities. For various reasons, Marie left her program and instead chose to work as a stripper. The author, at first troubled and yet fascinated by her friend's decision, follows Marie's journey ...

  2. 3D silicon strip detectors

    Energy Technology Data Exchange (ETDEWEB)

    Parzefall, Ulrich [Physikalisches Institut, Universitaet Freiburg, Hermann-Herder-Str. 3, D-79104 Freiburg (Germany)], E-mail: ulrich.parzefall@physik.uni-freiburg.de; Bates, Richard [University of Glasgow, Department of Physics and Astronomy, Glasgow G12 8QQ (United Kingdom); Boscardin, Maurizio [FBK-irst, Center for Materials and Microsystems, via Sommarive 18, 38050 Povo di Trento (Italy); Dalla Betta, Gian-Franco [INFN and Universita' di Trento, via Sommarive 14, 38050 Povo di Trento (Italy); Eckert, Simon [Physikalisches Institut, Universitaet Freiburg, Hermann-Herder-Str. 3, D-79104 Freiburg (Germany); Eklund, Lars; Fleta, Celeste [University of Glasgow, Department of Physics and Astronomy, Glasgow G12 8QQ (United Kingdom); Jakobs, Karl; Kuehn, Susanne [Physikalisches Institut, Universitaet Freiburg, Hermann-Herder-Str. 3, D-79104 Freiburg (Germany); Lozano, Manuel [Instituto de Microelectronica de Barcelona, IMB-CNM, CSIC, Barcelona (Spain); Pahn, Gregor [Physikalisches Institut, Universitaet Freiburg, Hermann-Herder-Str. 3, D-79104 Freiburg (Germany); Parkes, Chris [University of Glasgow, Department of Physics and Astronomy, Glasgow G12 8QQ (United Kingdom); Pellegrini, Giulio [Instituto de Microelectronica de Barcelona, IMB-CNM, CSIC, Barcelona (Spain); Pennicard, David [University of Glasgow, Department of Physics and Astronomy, Glasgow G12 8QQ (United Kingdom); Piemonte, Claudio; Ronchin, Sabina [FBK-irst, Center for Materials and Microsystems, via Sommarive 18, 38050 Povo di Trento (Italy); Szumlak, Tomasz [University of Glasgow, Department of Physics and Astronomy, Glasgow G12 8QQ (United Kingdom); Zoboli, Andrea [INFN and Universita' di Trento, via Sommarive 14, 38050 Povo di Trento (Italy); Zorzi, Nicola [FBK-irst, Center for Materials and Microsystems, via Sommarive 18, 38050 Povo di Trento (Italy)

    2009-06-01

    While the Large Hadron Collider (LHC) at CERN has started operation in autumn 2008, plans for a luminosity upgrade to the Super-LHC (sLHC) have already been developed for several years. This projected luminosity increase by an order of magnitude gives rise to a challenging radiation environment for tracking detectors at the LHC experiments. Significant improvements in radiation hardness are required with respect to the LHC. Using a strawman layout for the new tracker of the ATLAS experiment as an example, silicon strip detectors (SSDs) with short strips of 2-3 cm length are foreseen to cover the region from 28 to 60 cm distance to the beam. These SSD will be exposed to radiation levels up to 10{sup 15}N{sub eq}/cm{sup 2}, which makes radiation resistance a major concern for the upgraded ATLAS tracker. Several approaches to increasing the radiation hardness of silicon detectors exist. In this article, it is proposed to combine the radiation hard 3D-design originally conceived for pixel-style applications with the benefits of the established planar technology for strip detectors by using SSDs that have regularly spaced doped columns extending into the silicon bulk under the detector strips. The first 3D SSDs to become available for testing were made in the Single Type Column (STC) design, a technological simplification of the original 3D design. With such 3D SSDs, a small number of prototype sLHC detector modules with LHC-speed front-end electronics as used in the semiconductor tracking systems of present LHC experiments were built. Modules were tested before and after irradiation to fluences of 10{sup 15}N{sub eq}/cm{sup 2}. The tests were performed with three systems: a highly focused IR-laser with 5{mu}m spot size to make position-resolved scans of the charge collection efficiency, an Sr{sup 90}{beta}-source set-up to measure the signal levels for a minimum ionizing particle (MIP), and a beam test with 180 GeV pions at CERN. This article gives a brief overview of

  3. Optimizing the Stripping Procedure for LHCb

    CERN Document Server

    Richardson, Rachel

    2017-01-01

    The LHCb experiment faces a major challenge from the large amounts of data received while the LHC is running. The ability to sort this information in a useful manner is important for working groups to perform physics analyses. Both hardware and software triggers are used to decrease the data rate and then the stripping process is used to sort the data into streams and further into stripping lines. This project studies the hundreds of stripping lines to look for overlaps between them in order to make the stripping process more efficient.

  4. Studies of Heterogeneous Hydrothermal Stripping from Iron-loaded Naphthenic Acid-Alcohol-Kerosen

    Institute of Scientific and Technical Information of China (English)

    王兴尧; 康晓红; 谢慧琴; 卢立柱

    2003-01-01

    The technique of hydrothermal stripping from mixed aqueous-organic systems is a promising method for synthesizing oxide ceramic powders for high-performance applications. Some factors influencing heterogeneous hydrothermal stripping with water from iron-loaded organic phase of naphthenic acid-isooctyl alcohol-kerosene, such as initial concentrations of iron and naphthenic acid, concentration of Fe2O3 "seed", temperature and time, were investigated. Based on the experimental results, the rate equation was established. Nano-ferric oxide powders were obtained by the technique of hydrothermal stripping from the iron-loaded organic phase. The results suggest that the heterogeneous hydrothermal stripping proceeds in 3 steps: adsorption of naphthenic acid dimers and naphthenic complex of iron onto the surface of "seed", hydrolysis of adsorbed complex of iron, and condensation of hydrolyzed complex. The process activation energy is 115 kJ/mol and the heterogeneous hydrothermal stripping is controlled by a chemical reaction(the hydrolysis of naphthenic complex of iron).

  5. Solidification Structure of Low Carbon Steel Strips with Different Phosphorus Contents Produced by Strip Casting

    Institute of Scientific and Technical Information of China (English)

    Na LI; Zhenyu LIU; Yiqing QIU; Zhaosen LIN; Xianghua LIU; Guodong WANG

    2006-01-01

    In the present paper, low carbon steel strips with different phosphorus contents were produced using a twin roll strip casting process. The solidification structure was studied and its features were analyzed in detail. It was found that the strips possessed a fine microstructure compared with the mould cast steels. With increasing phosphorus content more ferrite has been formed with finer grains.

  6. Arsenic speciation in natural waters by cathodic stripping voltammetry.

    Science.gov (United States)

    Gibbon-Walsh, Kristoff; Salaün, Pascal; van den Berg, Constant M G

    2010-03-03

    Contamination of groundwater with arsenic (As) is a major health risk through contamination of drinking and irrigation water supplies. In geochemically reducing conditions As is mostly present as As(III), its most toxic species. Various methods exist to determine As in water but these are not suitable for monitoring arsenic speciation at its original pH and without preparation. We present a method that uses cathodic stripping voltammetry (CSV) to determine reactive As(III) at a vibrating, gold, microwire electrode. The As(III) is detected after adsorptive deposition of As(OH)(3)(0), followed by a potential scan to measure the reduction current from As(III) to As(0). The method is suitable for waters of pH 7-12, has an analytical range of 1 nM to 100 microM As (0.07-7500 ppb) and a limit of detection of 0.5 nM with a 60 s deposition time. The As speciation protocol involves measuring reactive As(III) by CSV at the original pH and acidification to pH 1 to determine inorganic As(III)+As(V) by anodic stripping voltammetry (ASV) using the same electrode. Total dissolved As is determined by ASV after UV-digestion at pH 1. The method was successfully tested on various raw groundwater samples from boreholes in the UK and West Bengal. Copyright 2010 Elsevier B.V. All rights reserved.

  7. Hardy inequalities in strips on ruled surfaces

    Directory of Open Access Journals (Sweden)

    2006-01-01

    Full Text Available We consider the Dirichlet Laplacian in infinite two-dimensional strips defined as uniform tubular neighbourhoods of curves on ruled surfaces. We show that the negative Gauss curvature of the ambient surface gives rise to a Hardy inequality and we use this to prove certain stability of spectrum in the case of asymptotically straight strips about mildly perturbed geodesics.

  8. Tactual Strip Maps as Navigational Aids.

    Science.gov (United States)

    Golledge, R. G.

    1991-01-01

    This article reviews the history and use of tactual maps by blind and visually impaired travelers. It discusses textual patterns, symbols, and graphics; differences between conventional geographic-cartographic maps and strip maps used as navigational aids; and current advances, including disposable, quick-to-produce, and easy-to-update strip maps.…

  9. 33 CFR 157.128 - Stripping system.

    Science.gov (United States)

    2010-07-01

    ... of the following devices for stripping oil from each cargo tank: (1) A positive displacement pump. (2) A self-priming centrifugal pump. (3) An eductor (4) Any other device accepted by the Commandant. (d... positive displacement pump or a self-priming centrifugal pump, the stripping system must have the...

  10. Water problems in Gaza Strip,Palestine

    Institute of Scientific and Technical Information of China (English)

    Ismail ALGHALBAN

    2001-01-01

    The only source for water in Gaza strip, southern Palestine, is the groundwater aquifer. The Pliocene - Pleistocene aquifer has two serious problems: quantity and quality. This study is an attempt to identify the problems and to suggest solutions for water problems in Gaza strip. In addition, some rules for rehabilitation of the aquifers were suggested.

  11. 7 CFR 29.6041 - Strips.

    Science.gov (United States)

    2010-01-01

    ... 7 Agriculture 2 2010-01-01 2010-01-01 false Strips. 29.6041 Section 29.6041 Agriculture Regulations of the Department of Agriculture AGRICULTURAL MARKETING SERVICE (Standards, Inspections, Marketing... INSPECTION Standards Definitions § 29.6041 Strips. The sides of a tobacco leaf from which the stem has...

  12. A direct in situ fingerprinting method for acid rock drainage using voltammetric techniques with a single renewable gold microelectrode.

    Science.gov (United States)

    Nuzzio, Donald B; Zettler, Erik R; Aguilera, Angeles; Amaral-Zettler, Linda A

    2011-04-15

    Electrochemistry allows for rapid identification of multiple metals and other chemical complexes common in acid rock drainage (ARD) systems. Voltammetric scans using a single gold microelectrode of water samples from geochemically distinct areas of the Río Tinto (RT) in southwestern Spain were clearly recognizable in the field and in samples stored at room temperature for over 6 months. Major voltammetric peaks of iron(III) and copper(II) were identified on a single constantly renewable gold microelectrode. Confirmation of these peaks was performed by spiking with standard metal solutions in the laboratory. This voltammetric technique is a rapid, direct and inexpensive in situ method for identification of water sources and their chemical characteristics, as well as an economical way to monitor environmental changes and remediation efforts.

  13. Fusion of Potentiometric & Voltammetric Electronic Tongue for Classification of Black Tea Taste based on Theaflavins (TF) Content

    Science.gov (United States)

    Bhattacharyya, Nabarun; Legin, Andrey; Papieva, Irina; Sarkar, Subrata; Kirsanov, Dmitry; Kartsova, Anna; Ghosh, Arunangshu; Bandyopadhyay, Rajib

    2011-09-01

    Black tea is an extensively consumed beverage worldwide with an expanding market. The final quality of black tea depends upon number of chemical compounds present in the tea. Out of these compounds, theaflavins (TF), which is responsible for astringency in black tea, plays an important role in determining the final taste of the finished black tea. The present paper reports our effort to correlate the theaflavins contents with the voltammetric and potentiometric electronic tongue (e-tongue) data. Noble metal-based electrode array has been used for collecting data though voltammetric electronic tongue where as liquid filled membrane based electrodes have been used for potentiometric electronic tongue. Black tea samples with tea taster score and biochemical results have been collected from Tea Research Association, Tocklai, India for the analysis purpose. In this paper, voltammetric and potentiometric e-tongue responses are combined to demonstrate improvement of cluster formation among tea samples with different ranges of TF values.

  14. Determination of total polyphenol index in wines employing a voltammetric electronic tongue

    Energy Technology Data Exchange (ETDEWEB)

    Ceto, Xavier [Sensors and Biosensors Group, Department of Chemistry, Universitat Autonoma de Barcelona, Edifici Cn, 08193 Bellaterra (Spain); Gutierrez, Juan Manuel [Bioelectronics Section, Department of Electrical Engineering, CINVESTAV, 07360 Mexico D.F. (Mexico); Gutierrez, Manuel [Instituto de Microelectronica de Barcelona (IMB-CNM), CSIC, 08193 Bellaterra (Spain); Cespedes, Francisco [Sensors and Biosensors Group, Department of Chemistry, Universitat Autonoma de Barcelona, Edifici Cn, 08193 Bellaterra (Spain); Capdevila, Josefina; Minguez, Santiago [Estacio de Viticultura i Enologia, INCAVI, Vilafranca del Penedes (Spain); Jimenez-Jorquera, Cecilia [Instituto de Microelectronica de Barcelona (IMB-CNM), CSIC, 08193 Bellaterra (Spain); Valle, Manel del, E-mail: manel.delvalle@uab.cat [Sensors and Biosensors Group, Department of Chemistry, Universitat Autonoma de Barcelona, Edifici Cn, 08193 Bellaterra (Spain)

    2012-06-30

    Highlights: Black-Right-Pointing-Pointer Array of voltammetric sensors modified with nanoparticles or conducting polymers. Black-Right-Pointing-Pointer It has been applied in wine analysis to predict polyphenol content index. Black-Right-Pointing-Pointer Uses data processing tools such as discrete wavelet transform and artificial neural network. Black-Right-Pointing-Pointer Identification of phenolics like gallic acid, catechin, caffeic acid, catechol. Black-Right-Pointing-Pointer Predicted polyphenol index agrees with Folin-Ciocalteau method and I{sub 280} index. - Abstract: This work reports the application of a voltammetric electronic tongue system (ET) made from an array of modified graphite-epoxy composites plus a gold microelectrode in the qualitative and quantitative analysis of polyphenols found in wine. Wine samples were analyzed using cyclic voltammetry without any sample pretreatment. The obtained responses were preprocessed employing discrete wavelet transform (DWT) in order to compress and extract significant features from the voltammetric signals, and the obtained approximation coefficients fed a multivariate calibration method (artificial neural network-ANN-or partial least squares-PLS-) which accomplished the quantification of total polyphenol content. External test subset samples results were compared with the ones obtained with the Folin-Ciocalteu (FC) method and UV absorbance polyphenol index (I{sub 280}) as reference values, with highly significant correlation coefficients of 0.979 and 0.963 in the range from 50 to 2400 mg L{sup -1} gallic acid equivalents, respectively. In a separate experiment, qualitative discrimination of different polyphenols found in wine was also assessed by principal component analysis (PCA).

  15. Voltammetric sensor for vanillylmandelic acid based on molecularly imprinted polymer-modified electrodes.

    Science.gov (United States)

    Blanco-López, M C; Lobo-Castañón, M J; Miranda-Ordieres, A J; Tuñón-Blanco, P

    2003-04-01

    Despite the increasing number of applications of molecularly imprinted polymers (MIPs) in analytical chemistry, the construction of a biomimetic voltammetric sensor remains still challenging. This work investigates the development of a voltammetric sensor for vanillylmandelic acid (VMA) based on acrylic MIP-modified electrodes. Thin layers of MIPs for VMA have been prepared by spin coating the surface of a glassy carbon electrode with the monomers mixture (template, methacrylic acid, a cross-linking agent and solvent), followed by in situ photopolymerisation. After extraction of the template molecule, the peak current recorded with the imprinted sensor after rebinding was linear with VMA concentration in the range 19-350 microg ml(-1), whereas the response of the control electrode is independent of incubation concentration, and was about one-tenth of the value recorded with the imprinted sensor at the maximum concentration tested. Under the conditions used, the sensor is able to differentiate between VMA and other closely structural-related compounds, such as 3-methoxy-4-hydroxyphenylethylene glycol (not detected), or 3,4- and 2,5-dihydroxyphenilacetic acids, which are adsorbed on the bare electrode surface but not at the polymer layer. Homovanillic acid was detected with the imprinted sensors after incubation, indicating that the presence of both methoxy and carboxylic groups in the same position as in VMA is necessary for effective binding in the imprinted sites. Nevertheless, both species can be differentiated by the oxidation potential. It can be concluded that MIP-based voltammetric electrodes are very promising analytical tool for the development of highly selective analytical sensors.

  16. Study on the adsorptive catalytic voltammetry of aloe-emodin at a carbon paste electrode

    Institute of Scientific and Technical Information of China (English)

    LI; Ju'nan; GAO; Peng; LI; Xiangling; YAN; Zhihong; MAO; Xu

    2005-01-01

    A new catalytic voltammetric method for the determination of anthraqunone medicines at a carbon paste electrode (CPE) was described for the first time. The mechanism of the catalytic reaction was investigated by using linear sweep voltammetry, cyclic voltammetry, constant potential electrolysis and so on. The experiment results indicate that aloe-emodin was efficiently accumulated at a CPE by adsorption. In the following potential scan, aloe-emodin was reduced to homologous anthrahydroquinone compound, then the compound was immediately oxidized to aloe-emodin by the dissolved oxygen, and the aloe-emodin was again reduced at the CPE. As a result, a cyclic catalytic reaction was established. But a reversible redox reaction of aloe-emodin can only be observed at a mercury electrode, no catalytic reaction occurs there. A sensitive catalytic voltammetric peak of aloe-emodin was obtained at about -0.60 V (vs. SCE) in 0.56 mol/L NH3-NH4Cl buffer (pH 8.9). The proposed method was applied to the determination of aloe-emodin in the Radix Rhei with satisfactory results. The determination results were in good agreement with reference values obtained by the HPLC. The adsorptive catalytic voltammetry for the determination of organic compound at CPE, chemically modified electrode and other solid electrodes could be significant in the studies on pharmacology, pharmacodynamics, toxicity of medicine, clinical medicine and biochemistry.

  17. A New Voltammetric Enzyme Immunoassay System for the Detection of Alkaline Phosphatase

    Institute of Scientific and Technical Information of China (English)

    KuiJIAO; WeiSUN; 等

    2002-01-01

    A new voltammetric enzyme immunoassay system was invesigated based on p-nitrophenyl phosphate (PNPP) as the subsrate for alkaline phosphatase (ALP). PNPP is enzymatically hydrolyzed and the product p-nitrophenol (PNP) is detected by differential pulse voltammetry (DPV), which can be oxidized at +1.02 V(vs.Ag/AgCl) on bare glass carbon electrode (GCE). The conditions for enzymatic reaction and electrochemical detection were studied. According to this method,ALP can be detected with a detection limit of 2.8×102 mU/L and a linear range of 4.0×102-1.0×106mU/L.

  18. A New Voltammetric Enzyme Immunoassay System for the Detection of Alkaline Phosphatase

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A new voltammetric enzyme immunoassay system was investigated based on p-nitrophenyl phosphate (PNPP) as the substrate for alkaline phosphatase (ALP). PNPP is enzymatically hydrolyzed and the product p-nitrophenol (PNP) is detected by differential pulse voltammetry (DPV), which can be oxidized at +1.02 V (vs. Ag/AgCl) on bare glass carbon electrode (GCE). The conditions for enzymatic reaction and electrochemical detection were studied. According to this method, ALP can be detected with a detection limit of 2.8′102 mU/L and a linear range of 4.0′102 ~ 1.0′106 mU/L.

  19. Adsorption,Oxdation and Complexation of Water—So—Luble Organic Substances in Soils

    Institute of Scientific and Technical Information of China (English)

    DINGCHANG-PU

    1995-01-01

    A greater part of water-soluble organic substances,accounting for 60-70% of the total,could be adsorbed by soils,which included strongly and weekly reducing substances,positively and negatively charged substances and substances containing amido.There existed a tendency of decrease in adsorption of the negatively charged organic substances by the soil from South China to North China,with expression as Coulombian adsorption.A simulatneous reduction of iron and manganese appeared with clear voltammertric behaviours upon oxidation of water-soluble organic substances,Complexation of organic ligands with ferrous iron and manganous manganee was proved by differential pulse voltammetric method,with disappearance of oxidation peaks of ferrous iron and manganous manganese at 0.00 V and 0.35 V and occurrence of Fe2+-complex and Mn2+-complex at 0l75 V and 1.2V respectively,whose peak potentials shifted backward.

  20. Circuit realization microwave antennas-oscillator on strip antennas

    OpenAIRE

    Golynskyy, V. D.; Prudyus, I. N.

    2009-01-01

    Showing special feature of development circuitries microwave transistors antennasoscillator on strip dielectric-resonator-antennas. Showing circuitries and technical characteristics of developed microwave antennasoscillator on strip.

  1. Analytical procedure for the simultaneous voltammetric determination of trace metals in food and environmental matrices. Critical comparison with atomic absorption spectroscopic measurements.

    Science.gov (United States)

    Melucci, Dora; Torsi, Giancarlo; Locatelli, Clinio

    2007-01-01

    An analytical procedure fit for the simultaneous determination of copper (II), chromium(VI), thallium(I), lead(II), tin(II), antimony(III), and zinc(II) by square wave anodic stripping voltammetry (SWASV) in three interdependent environmental matrices involved in foods and food chain as meals, cereal plants and soils is described. The digestion of each matrix was carried out using a concentrated HCl-HNO3-H2SO4 (meals and cereal plants) and HCl-HNO3 (soils) acidic attack mixtures. 0.1 mol/L dibasic ammonium citrate pH 8.5 was employed as the supporting electrolyte. The voltammetric measurements were carried out using, as working electrode, a stationary hanging mercury drop electrode (HMDE) and a platinum electrode and an Ag/AgCl/KClsat electrode as auxiliary and reference electrodes, respectively. The analytical procedure was verified by the analyses of the standard reference materials: Wholemeal BCR-CRM 189, Tomato Leaves NIST-SRM 1573a and Montana Soil Moderately Elevated Traces NIST-SRM 2711. For all the elements in the certified matrix, the precision as repeatability, expressed as relative standard deviation (Sr %) was lower than 5%. The accuracy, expressed as percentage relative error (e %) was of the order of 3-7%, while the detection limits were in the range 0.015-0.103 microg/g. Once set up on the standard reference materials, the analytical procedure was transferred and applied to commercial meal samples, cereal plants and soils samples drawn in sites devoted to agricultural practice. A critical comparison with spectroscopic measurements is also discussed.

  2. Transfusion and blood donation in comic strips.

    Science.gov (United States)

    Lefrère, Jean-Jacques; Danic, Bruno

    2013-07-01

    The representation of blood transfusion and donation of blood in the comic strip has never been studied. The comic strip, which is a relatively recent art, emerged in the 19th century before becoming a mass medium during the 20th century. We have sought, by calling on collectors and using the resources of Internet, comic strips devoted, wholly or in part, to the themes of transfusion and blood donation. We present some of them here in chronologic order, indicating the title, country of origin, year of publication, and names of authors. The theme of the superhero using transfusion to transmit his virtues or his powers is repeated throughout the 20th century in North American comic strips. More recently, comic strips have been conceived from the outset with a promotional aim. They perpetuate positive images and are directed toward a young readership, wielding humor to reduce the fear of venipuncture. Few comic strips denounce the abuse of the commercialization of products derived from the human body. The image of transfusion and blood donation given by the comic strips is not to be underestimated because their readership is primarily children, some of whom will become blood donors. Furthermore, if some readers are transfused during their lives, the impact of a memory more or less conscious of these childhood readings may resurface, both in hopes and in fears.

  3. A Strip Cell in Pyroelectric Devices

    Directory of Open Access Journals (Sweden)

    An-Shen Siao

    2016-03-01

    Full Text Available The pyroelectric effect affords the opportunity to convert temporal temperature fluctuations into usable electrical energy in order to develop abundantly available waste heat. A strip pyroelectric cell, used to enhance temperature variation rates by lateral temperature gradients and to reduce cell capacitance to further promote the induced voltage, is described as a means of improving pyroelectric energy transformation. A precision dicing saw was successfully applied in fabricating the pyroelectric cell with a strip form. The strip pyroelectric cell with a high-narrow cross section is able to greatly absorb thermal energy via the side walls of the strips, thereby inducing lateral temperature gradients and increasing temperature variation rates in a thicker pyroelectric cell. Both simulation and experimentation show that the strip pyroelectric cell improves the electrical outputs of pyroelectric cells and enhances the efficiency of pyroelectric harvesters. The strip-type pyroelectric cell has a larger temperature variation when compared to the trenched electrode and the original type, by about 1.9 and 2.4 times, respectively. The measured electrical output of the strip type demonstrates a conspicuous increase in stored energy as compared to the trenched electrode and the original type, by of about 15.6 and 19.8 times, respectively.

  4. Differential pulse voltammetric determination of acyclovir in pharmaceutical preparations using a pencil graphite electrode.

    Science.gov (United States)

    Dilgin, Didem Giray; Karakaya, Serkan

    2016-06-01

    In this study, a new selective and sensitive voltammetric procedure for determination of acyclovir (ACV) was proposed using a disposable electrode, pencil graphite electrode (PGE). Cyclic and differential pulse voltammograms of ACV were recorded in Britton-Robinson buffer solution containing 0.10 M KCl with pH of 4.0 at PGE. The PGE displayed a very good electrochemical behavior with significant enhancement of the peak current compared to a glassy carbon electrode (GCE). Under experimental conditions, the PGE had a linear response range from 1.0 μM to 100.0 μM ACV with a detection limit of 0.3 μM (based on 3 Sb). Relative standard deviations of 4.8 and 3.6% were obtained for five successive determinations of 10.0 and 50.0 μM ACV, respectively, which indicate acceptable repeatability. This voltammetric method was successfully applied to the direct determination of ACV in real pharmaceutical samples. The effect of various interfering compounds on the ACV peak current was studied.

  5. Sensitive voltammetric detection of yeast RNA based on its interaction with Victoria Blue B

    Directory of Open Access Journals (Sweden)

    WEI SUN

    2009-12-01

    Full Text Available Voltammetric studies of the interaction of yeast RNA (y-RNA with Victoria Blue B (VBB are described in this paper. Furthermore, a linear sweep voltammetric method for the detection of y-RNA was established. The reaction conditions, such as acidity and amount of buffer solution, the concentration of VBB, the reaction time and temperature, etc., were carefully investigated by second order derivative linear sweep voltammetry. Under the optimal conditions, the reduction peak current of VBB at –0.75 V decreased greatly after the addition of y-RNA to the solution without any shift of the reduction peak potential. Based on the decrease of the peak current, a new quantitative method for the determination of y-RNA was developed. The effects of co-existing substances on the determination were carefully investigated and three synthetic samples were determined with satisfactory results. The stoichiometry of the VBB–y-RNA complex was calculated by linear sweep voltammetry and the interaction mechanism is discussed.

  6. Determination of total polyphenol index in wines employing a voltammetric electronic tongue.

    Science.gov (United States)

    Cetó, Xavier; Gutiérrez, Juan Manuel; Gutiérrez, Manuel; Céspedes, Francisco; Capdevila, Josefina; Mínguez, Santiago; Jiménez-Jorquera, Cecilia; del Valle, Manel

    2012-06-30

    This work reports the application of a voltammetric electronic tongue system (ET) made from an array of modified graphite-epoxy composites plus a gold microelectrode in the qualitative and quantitative analysis of polyphenols found in wine. Wine samples were analyzed using cyclic voltammetry without any sample pretreatment. The obtained responses were preprocessed employing discrete wavelet transform (DWT) in order to compress and extract significant features from the voltammetric signals, and the obtained approximation coefficients fed a multivariate calibration method (artificial neural network-ANN-or partial least squares-PLS-) which accomplished the quantification of total polyphenol content. External test subset samples results were compared with the ones obtained with the Folin-Ciocalteu (FC) method and UV absorbance polyphenol index (I(280)) as reference values, with highly significant correlation coefficients of 0.979 and 0.963 in the range from 50 to 2400 mg L(-1) gallic acid equivalents, respectively. In a separate experiment, qualitative discrimination of different polyphenols found in wine was also assessed by principal component analysis (PCA).

  7. Voltammetric behavior of nitrofurazone and its hydroxymethyl prodrug with potential anti-Chagas activity

    Energy Technology Data Exchange (ETDEWEB)

    La-Scalea, Mauro Aquiles [Sao Paulo Univ., SP (Brazil). Faculdade de Ciencias Farmaceuticas; Sao Paulo Univ., SP (Brazil). Inst. de Quimica]. E-mail: scalea@usp.br; Menezes, Carla Maria de Souza; Ferreira, Elizabeth Igne [Sao Paulo Univ., SP (Brazil). Faculdade de Ciencias Farmaceuticas; Juliao, Murilo Sergio da Silva [Sao Paulo Univ., SP (Brazil). Inst. de Quimica; Universidade Estadual Vale do Acaraju, Fortaleza, CE (Brazil). Centro de Ciencias Exatas e Tecnologicas; Man Chin Chung [UNESP, Araraquara, SP (Brazil). Faculdade de Ciencias Farmaceuticas; Serrano, Silvia Helena Pires [Sao Paulo Univ., SP (Brazil). Inst. de Quimica

    2005-07-15

    Chagas' disease is a serious health problem for Latin America. The situation is worsened by the lack of efficient chemotherapy. The two available commercial drugs, benznidazole and nifurtimox, are more effective in the acute phase of the disease. Nitrofurazone is active against Trypanosoma cruzi, however its high toxicity precludes its current use in parasitosis. Hydroxymethyl nitrofurazone is a prodrug of nitrofurazone. It is more active against Trypanosoma cruzi than nitrofurazone, besides being less toxic. This work shows the voltammetric behavior of nitrofurazone and a comparison with those of metronidazole and chloramphenicol using cyclic, linear sweep and differential pulse voltammetries. For these drugs also the prediction of the diffusion coefficients using Wilke-Chang equation was performed. The reduction of nitrofurazone is pH-dependent and in acidic medium the hydroxylamine derivative, involving four electrons, is the principal product formed. In aqueous-alkaline medium and with a glassy carbon electrode pre-treatment the reduction of nitrofurazone occurs in two steps, the first involving one electron to form the nitro-radical anion and the second corresponding to the hydroxylamine derivative formation. Hydroxymethyl nitrofurazone presented the same voltammetric behavior and electroactivity, indicating that the molecular modification performed in nitrofurazone did not change its capacity to be reduced. A brief discussion regarding the differences in biological activity between the two compounds is also presented. (author)

  8. Copper(II) complexes of prion protein PEG11-tetraoctarepeat fragment: spectroscopic and voltammetric studies.

    Science.gov (United States)

    Bonomo, Raffaele P; Di Natale, Giuseppe; Rizzarelli, Enrico; Tabbì, Giovanni; Vagliasindi, Laura I

    2009-04-14

    Spectroscopic (UV-Vis and EPR) and voltammetric studies have been carried out on the copper(II) complexes with the Ac-PEG11-(PHGGGWGQ)4-NH2 (L) polypeptide. In the ratios Cu : L 3 : 1 and 4 : 1, the two [Cu3(L)H(-6)] and [Cu4(L)H(-8)] complex species have been characterized at neutral pH values. All the copper atoms occupy similar coordination sites formed by imidazole, peptidic nitrogen atoms and carbonyl oxygen atoms in a square base pyramidal geometry. Voltammetric measurements on these systems point out the cooperativity in the electron transfer processes among the copper(II) sites during their reduction. NO interaction with these polynuclear copper species is characterized by the reduction of the copper sites through the formation of two different intermediate complex species. When an excess of the Ac-PEG11-(PHGGGWGQ)4-NH2 ligand is considered, frozen solution EPR parameters and UV-Vis spectroscopic data identify the [Cu(N(im))4]2+ chromophore, which does not interact with NO.

  9. Manganese dioxide-graphene nanocomposite film modified electrode as a sensitive voltammetric sensor of indomethacin detection

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yuxia; Zhang, Zhenfa; Zhang, Cuizong; Huang, Wei; Liang, Caiyun; Peng, Jinyun [Guangxi Normal University for Nationalities, Chongzuo (China)

    2016-08-15

    Excess amount of analgesic and anti-inflammatory drug, such as indomethacin, often leads to serious gastrointestinal complications; therefore, amount of such active compound should be regulated in commercial drugs. This study proposes an efficient analytical technique to detect indomethacin selectively. We prepared and investigated electrochemical properties of a manganese dioxide-graphene nanocomposite film modified glassy carbon electrode (MnO{sub 2}-Gr/GCE). The behavior of the modified electrode as electrocatalyst towards indomethacin oxidation was also examined. The cyclic voltammetric results reveal that the electrocatalytic activity for the oxidation of indomethacin can significantly be enhanced on the MnO{sub 2}-Gr/GCE. Indomethacin exhibited a sensitive anodic peak at about 0.90 V at MnO{sub 2}-Gr/GCE. The data obtained from differential pulse voltammetry showed that the anodic peak currents were linearly dependent on the indomethacin concentrations in the range of 1.0 X 10{sup -7} to 2.5 X 10{sup -5} mol/L with a detection limit of 3.2 X 10{sup -8} mol/L (S/N = 3). Most importantly, the proposed method shows efficient and selective sensing of indomethacin in commercial harmaceutical formulations. This is the first report of a voltammetric sensor for indomethacin using MnO{sub 2}-Gr/GCE. We believe that this new method can be commercialized for routine applications in laboratories.

  10. Microgravimetric and voltammetric study of Zn underpotential deposition on platinum in alkaline medium

    Science.gov (United States)

    Calegaro, M. L.; Santos, M. C.; Miwa, D. W.; Machado, S. A. S.

    2005-03-01

    The microgravimetric and voltammetric responses of a polycrystalline Pt electrode in 0.1 mol L -1 NaOH solution in the presence and the absence of 1.6 × 10 -4 Zn 2+, at 0.1 V s -1 were analyzed. During the positive potential sweep, the water molecules are progressively substituted by OH - ions, prior to PtO formation. The voltammetric charges obtained under the Zn ads dissolution peaks suggest that 0.7 monolayers are deposited, with each Zn ad-atom occupying one active site and transferring two electrons. The total loss of mass due to the dissolution of the Zn ad-layer was 136.6 ng cm -2 and the mass increase due to PtO formation was found to be only 12 ng cm -2 less than the theoretical ones, 157.5 and 37.4 ng cm -2, respectively, indicating that both processes are overlapped. In this way it is proposed that an adsorbed by-layer of Zn and OH - ions is formed.

  11. Vapor permeation-stepwise injection simultaneous determination of methanol and ethanol in biodiesel with voltammetric detection.

    Science.gov (United States)

    Shishov, Andrey; Penkova, Anastasia; Zabrodin, Andrey; Nikolaev, Konstantin; Dmitrenko, Maria; Ermakov, Sergey; Bulatov, Andrey

    2016-02-01

    A novel vapor permeation-stepwise injection (VP-SWI) method for the determination of methanol and ethanol in biodiesel samples is discussed. In the current study, stepwise injection analysis was successfully combined with voltammetric detection and vapor permeation. This method is based on the separation of methanol and ethanol from a sample using a vapor permeation module (VPM) with a selective polymer membrane based on poly(phenylene isophtalamide) (PA) containing high amounts of a residual solvent. After the evaporation into the headspace of the VPM, methanol and ethanol were transported, by gas bubbling, through a PA membrane to a mixing chamber equipped with a voltammetric detector. Ethanol was selectively detected at +0.19 V, and both compounds were detected at +1.20 V. Current subtractions (using a correction factor) were used for the selective determination of methanol. A linear range between 0.05 and 0.5% (m/m) was established for each analyte. The limits of detection were estimated at 0.02% (m/m) for ethanol and methanol. The sample throughput was 5 samples h(-1). The method was successfully applied to the analysis of biodiesel samples.

  12. High energy H- ion transport and stripping

    Energy Technology Data Exchange (ETDEWEB)

    Chou, W.; /Fermilab

    2005-05-01

    During the Proton Driver design study based on an 8 GeV superconducting RF H{sup -} linac, a major concern is the feasibility of transport and injection of high energy H{sup -} ions because the energy of H{sup -} beam would be an order of magnitude higher than the existing ones. This paper will focus on two key technical issues: (1) stripping losses during transport (including stripping by blackbody radiation, magnetic field and residual gases); (2) stripping efficiency of carbon foil during injection.

  13. THE DEVELOPMENT OF FCC STRIPPING TECHNOLOGY

    Institute of Scientific and Technical Information of China (English)

    ZHANGZhen-qian

    2003-01-01

    This article briefly describes the major patents domestic and the abroad,and the current situation and achievements of FCC stripping technology in China.The develping trend of FCC stripping technology is presented,including further developments of FCC stripper to improve unit performance,combination of the stripper and pre-stripper within disengager to from a complete high-efficiency FCC stripping system.In addition to high efficiency,simple structure and easiness of installation and maintenance for a new FCC stripper are all of consideration.

  14. Saving Energy Through Advanced Power Strips (Poster)

    Energy Technology Data Exchange (ETDEWEB)

    Christensen, D.

    2013-10-01

    Advanced Power Strips (APS) look just like ordinary power strips, except that they have built-in features that are designed to reduce the amount of energy used by many consumer electronics. There are several different types of APSs on the market, but they all operate on the same basic principle of shutting off the supply power to devices that are not in use. By replacing your standard power strip with an APS, you can signifcantly cut the amount of electricity used by your home office and entertainment center devices, and save money on your electric bill. This illustration summarizes the different options.

  15. Inapproximability of maximal strip recovery

    CERN Document Server

    Jiang, Minghui

    2009-01-01

    In comparative genomic, the first step of sequence analysis is usually to decompose two or more genomes into syntenic blocks that are segments of homologous chromosomes. For the reliable recovery of syntenic blocks, noise and ambiguities in the genomic maps need to be removed first. Maximal Strip Recovery (MSR) is an optimization problem proposed by Zheng, Zhu, and Sankoff for reliably recovering syntenic blocks from genomic maps in the midst of noise and ambiguities. Given $d$ genomic maps as sequences of gene markers, the objective of \\msr{d} is to find $d$ subsequences, one subsequence of each genomic map, such that the total length of syntenic blocks in these subsequences is maximized. For any constant $d \\ge 2$, a polynomial-time 2d-approximation for \\msr{d} was previously known. In this paper, we show that for any $d \\ge 2$, \\msr{d} is APX-hard, even for the most basic version of the problem in which all gene markers are distinct and appear in positive orientation in each genomic map. Moreover, we provi...

  16. A video strip chart program

    Energy Technology Data Exchange (ETDEWEB)

    Jones, N.L. [Oak Ridge National Lab., TN (United States). Accelerator-Based Atomic Physics

    1994-12-31

    A strip chart recorder has been utilized for trend analysis of the Oak Ridge National Laboratory EN tandem since 1987. At the EN, the author could not afford the nice eight channel thermal pen recorder that was used at the 25 URC. He had to suffice with two channel fiber tip or capillary pen type recorders retrieved from salvage and maintained with parts from other salvaged recorders. After cycling through several machines that eventually became completely unserviceable, a search for a new thermal recorder was begun. As much as he hates to write computer code, he decided to try his hand at getting an old data acquisition unit, that had been retrieved several years ago from salvage, to meet his needs. A BASIC language compiler was used because time was not available to learn a more advanced language. While attempting to increase acquisition and scroll speed on the 6 MHz 80286 that the code was first developed on, it became apparent that scrolling only the first small portion of the screen at high speed and then averaging that region and histogramming the average provided both the speed necessary for capturing fairly short duration events, and a trend record without use of back scrolling and disk storage routines. This turned out to be quite sufficient.

  17. Determination of mercury in hair by square-wave anodic stripping voltammetry at a rotating gold disk electrode after microwave digestion.

    Science.gov (United States)

    East, Gaston A; Marinho, Epitácio P

    2005-03-01

    A simple and reliable method for the determination of mercury in hair on a rotating gold disk electrode using subtractive anodic stripping voltammetry without removal of oxygen is reported. Voltammetric and microwave parameters were optimized to obtain the best analytical results. Parameters such as supporting electrolyte concentration, influence of chloride in the Hg peak, deposition potential, scan rate, accumulation time, rotation rate, square-wave amplitude, and electrode conditioning were studied. Pressurized microwave-assisted digestion of hair, suitable for the accurate voltammetric determination of Hg, was evaluated using six acid mixtures and several time-power programs. Under the optimized conditions, no interference by copper, cadmium, lead, nickel, manganese, iron, or zinc was found at concentrations corresponding to their occurrence in normal hair. A calibration plot between 6,67 and 46,69 microg/L was linear, with r(2) better than 0.999. The detection limit for a deposition time of 60 s at 254 g was calculated as 1.92 nM (3omega). Validation of the method was demonstrated with the use of a certified reference sample of hair. Eight real samples of hair (four unexposed children and four exposed persons) were also analyzed.

  18. Anodic voltammetric behavior and determination of rosiglitazone in pharmaceutical dosage forms and biological fluids on solid electrode.

    Science.gov (United States)

    Dogan-Topal, Burcu; Tuncel, Secil; Ozkan, Sibel A

    2010-09-01

    The anodic voltammetric behavior and electroanalytical determination of rosiglitazone was studied using cyclic, linear sweep, differential pulse and square wave voltammetric techniques on glassy carbon electrode. The oxidation of rosiglitazone was irreversible and exhibited diffusion controlled process depending on pH. Different parameters were tested to optimize the conditions for the determination of the oxidation mechanism of rosiglitazone. The dependence of current intensities and potentials on pH, concentration, scan rate, nature of the buffer was also investigated. According to the linear relationship between the peak current and the concentration, differential pulse and square wave voltammetric methods for rosiglitazone assay in pharmaceutical dosage forms and biological fluids were developed. A linear response was obtained within the range of 1x10-6M - 6x10-5M in 0.1 M H2SO4 and acetate buffer at pH 5.70 for both voltammetric methods in human serum samples. The practical analytical value of the method is demonstrated by quantitative determination of rosiglitazon in pharmaceutical formulation and human serum, without the need for separation or complex sample preparation, since there was no interference from the excipients and endogenous substances. The methods were fully validated and successfully applied to the high throughput determination of the drug in tablets and human serum with good recoveries.

  19. Cathodic Voltammetric Behavior of Pillar[5]quinone in Nonaqueous Media. Symmetry Effects on the Electron Uptake Sequence.

    Science.gov (United States)

    Cheng, Beijun; Kaifer, Angel E

    2015-08-12

    The cathodic voltammetric behavior of pillar[5]quinone was investigated in dichloromethane solution. Our data show that the symmetry of the macrocycle has a pronounced effect on the electron uptake sequence. The uptake of the first five electrons follows a 2-1-2 pattern, and only a total of eight electrons could be injected into the macrocycle under our experimental conditions.

  20. Interfacial adsorption of insulin - Conformational changes and reversibility of adsorption

    NARCIS (Netherlands)

    Mollmann, SH; Jorgensen, L; Bukrinsky, JT; Elofsson, U; Norde, W; Frokjaer, S

    2006-01-01

    The adsorption of human insulin to Teflon particles was studied with respect to conformational changes and the reversibility of adsorption was examined by total internal reflection fluorescence (TIRF). Adsorption isotherms for the adsorption of human insulin indicated high affinity adsorption, even

  1. Interfacial adsorption of insulin. Conformational changes and reversibility of adsorption

    NARCIS (Netherlands)

    Mollmann, S.H.; Bukrinsky, J.T.; Elofsson, U.; Norde, W.; Frokjaer, S.

    2006-01-01

    The adsorption of human insulin to Teflon particles was studied with respect to conformational changes and the reversibility of adsorption was examined by total internal reflection fluorescence (TIRF). Adsorption isotherms for the adsorption of human insulin indicated high affinity adsorption, even

  2. Plaque accumulations caused by interdental stripping.

    Science.gov (United States)

    Radlanski, R J; Jäger, A; Schwestka, R; Bertzbach, F

    1988-11-01

    Human enamel surfaces were stripped with orthodontic grinding and finishing materials, and evaluated with the scanning electron microscope (SEM). Even under in vitro conditions with the finest finishing strips, it was not possible to produce an enamel surface free of the furrows that result from the initial abrasion caused by the coarse strip. Enamel surfaces stripped gradually from coarse to superfine were left in the mouths of patients for 12 weeks and evaluated with the SEM. The edges of the furrows were found to be smoother but the furrows remained wide and deep enough to facilitate more plaque accumulations than those on untreated surfaces. The use of dental floss did not result in prevention of plaque accumulations along the bottom of the furrows.

  3. Finite element modeling of corneal strip extensometry

    CSIR Research Space (South Africa)

    Botha, N

    2012-12-01

    Full Text Available numerically modelled in several studies, this study focusses on accurately modelling the strip extensiometry test. Two methods were considered to simulate the experimental conditions namely, a single phase and a two phase method. A finite element model...

  4. Catalytic hydrogen evolution in cathodic stripping voltammetry on a mercury electrode in the presence of cobalt(II) ion and phenylthiourea or thiourea.

    Science.gov (United States)

    Spătaru, N; Bănica, F G

    2001-11-01

    The system Co(II)-phenylthiourea (PTU)-borax buffer was investigated by cathodic stripping voltammetry (CSV) at a hanging mercury drop electrode. The results of the voltammetric measurements showed that the presence of both PTU and Co(II) gives rise to a new irreversible peak at about -1.5 V. Based upon our previous results obtained in the study of other sulfur compounds and the sulfide ion itself, the peak was ascribed to the catalytic hydrogen evolution superimposed on the reduction of the coordinated Co(II) ion. The catalyst itself is a Co(II) complex with the sulfide ion produced by the decomposition of the analyte during the deposition step. The influence of PTU and cobalt concentration, accumulation conditions and stripping parameters was investigated and complementary data on thiourea are included. The results showed that the measurement of the catalytic hydrogen evolution peak current can be used as a basis for a simple, accurate and rapid method for the determination of PTU within the concentration range 10-100 nM. The catalytic method is relatively free of interferences and could be a suitable alternative for cases in which the stripping peak due to mercury ion reduction in the accumulated mercury compound is disturbed by some interference.

  5. Strip Casting of High Performance Structural Alloys

    Institute of Scientific and Technical Information of China (English)

    S S Park; J G Lee; Nack J Kim

    2004-01-01

    There exists a great need for the development of high performance alloys due to increasing demands for energy conservation and environmental protection. Application of strip casting shows a strong potential for the improvement of properties of existing alloys and also for the development of novel alloy systems with superior properties. The present paper reviews our Center's activities in the development of high performance alloys by strip casting. Examples include (1) Al alloys, (2) wrought Mg alloys, and (3) bulk metallic glass (BMG) alloys.

  6. Speed Control and Coiling Temperature Control of Strip

    Institute of Scientific and Technical Information of China (English)

    CAI Xiao-hui; ZHANG Dian-hua; WANG Guo-dong; LIU Xiang-hua; FAN Lei

    2004-01-01

    Considering the strip speed during controlled laminar cooling on Baosteel 1580 hot strip mill in China, the influence of strip speed fluctuation on coiling temperature control for the tail and "neck" of the strip was analyzed. The optimization strategies were put forward and proved effective in operation.

  7. Excess Production Capacity Squeezes Profits of Brass Strip Enterprises

    Institute of Scientific and Technical Information of China (English)

    2012-01-01

    <正>Between 2003 and 2006,under the backdrop of rapid growth of domestic demand for brass strip and soaring copper price,brass strip manufacturers made a fortune.And brass strip manufacturers mushroomed in Zhejiang,Anhui and Jiangsu.Large brass strip manufacturers

  8. Process development of thin strip steel casting

    Energy Technology Data Exchange (ETDEWEB)

    Sussman, R.C.; Williams, R.S.

    1990-12-01

    An important new frontier is being opened in steel processing with the emergence of thin strip casting. Casting steel directly to thin strip has enormous benefits in energy savings by potentially eliminating the need for hot reduction in a hot strip mill. This has been the driving force for numerous current research efforts into the direct strip casting of steel. The US Department of Energy initiated a program to evaluate the development of thin strip casting in the steel industry. In earlier phases of this program, planar flow casting on an experimental caster was studied by a team of engineers from Westinghouse Electric corporation and Armco Inc. A subsequent research program was designed as a fundamental and developmental study of both planar and melt overflow casting processes. This study was arranged as several separate and distinct tasks which were often completed by different teams of researchers. An early task was to design and build a water model to study fluid flow through different designs of planar flow casting nozzles. Another important task was mathematically modeling of melt overflow casting process. A mathematical solidification model for the formation of the strip in the melt overflow process was written. A study of the material and conditioning of casting substrates was made on the small wheel caster using the melt overflow casting process. This report discusses work on the development of thin steel casting.

  9. Process development of thin strip steel casting

    Energy Technology Data Exchange (ETDEWEB)

    Sussman, R.C.; Williams, R.S.

    1990-12-01

    An important new frontier is being opened in steel processing with the emergence of thin strip casting. Casting steel directly to thin strip has enormous benefits in energy savings by potentially eliminating the need for hot reduction in a hot strip mill. This has been the driving force for numerous current research efforts into the direct strip casting of steel. The US Department of Energy initiated a program to evaluate the development of thin strip casting in the steel industry. In earlier phases of this program, planar flow casting on an experimental caster was studied by a team of engineers from Westinghouse Electric corporation and Armco Inc. A subsequent research program was designed as a fundamental and developmental study of both planar and melt overflow casting processes. This study was arranged as several separate and distinct tasks which were often completed by different teams of researchers. An early task was to design and build a water model to study fluid flow through different designs of planar flow casting nozzles. Another important task was mathematically modeling of melt overflow casting process. A mathematical solidification model for the formation of the strip in the melt overflow process was written. A study of the material and conditioning of casting substrates was made on the small wheel caster using the melt overflow casting process. This report discusses work on the development of thin steel casting.

  10. Activated Carbon Preparation and Modification for Adsorption

    Science.gov (United States)

    Cao, Yuhe

    Butanol is considered a promising, infrastructure-compatible biofuel. Butanol has a higher energy content than ethanol and can be used in conventional gas engines without modifications. Unfortunately, the fermentation pathway for butanol production is restricted by its toxicity to the microbial strains used in the process. Butanol is toxic to the microbes, and this can slow fermentation rates and reduce butanol yields. Gas stripping technology can efficiently remove butanol from the fermentation broth as it is produced, thereby decreasing its inhibitory effects. Traditional butanol separation heavily depends on the energy intensive distillation method. One of the main issues in acetone-butanol-ethanol fermentation is that butanol concentrations in the fermentation broth are low, ranging from 1 to 1.2 percent in weight, because of its toxicity to the microorganisms. Therefore distillation of butanol is even worse than distillation of corn ethanol. Even new separation methods, such as solid- extraction methods involve adding substances, such as polymer resin and zeolite or activated carbon, to biobutanol fermentatioon broth did not achieve energy efficient separation of butanol due to low adsorption selectivity and fouling in broth. Gas-stripping - condensation is another new butanol recovery method, however, the butanol in gas-stripping stream is too low to be condensed without using expensive and energy intensive liquid nitrogen. Adsorption can then be used to recover butanol from the vapor phase. Activated carbon (AC) samples and zeolite were investigated for their butanol vapor adsorption capacities. Commercial activated carbon was modified via hydrothermal H2O2 treatment, and the specific surface area and oxygen-containing functional groups of activated carbon were tested before and after treatment. Hydrothermal H2O 2 modification increased the surface oxygen content, Brunauer-Emmett-Teller surface area, micropore volume, and total pore volume of active carbon

  11. Determination of brilliant blue FCF in the presence and absence of erythrosine and quinoline yellow food colours by cathodic stripping voltammetry.

    Science.gov (United States)

    Florian, M; Yamanaka, H; Carneiro, P A; Zanoni, M Valnice Boldrin

    2002-09-01

    A study of the voltammetric behaviour of the food colours brilliant blue FCF (C.I. 42090), erythrosine (C.I. 45430) and quinoline yellow (C.I. 47005) in the pH range 2-10 have been carried out by cathodic#10; stripping voltammetry. At pH 4.5 (acetate buffer) with an accumulation potential of 0 V and accumulation time of 30s, the voltammograms presented well-defined reduction peaks at potential - 0.76 V for brilliant blue FCF, - 0.85 V for quinoline yellow and - 0.54 V for erythrosine. Linear calibration graphs were obtained from 8 to 80 microg l(-1) brilliant blue, from 4 to 43 microg l(-1) quinoline yellow and from 10 to 70 microg l(-1) erythrosine. The method has been successfully applied to identify and quantify binary mixtures of these dyes and applied for determining brilliant blue FCF in commercial food products.

  12. Novel photoresist stripping technology using steam-water mixture*

    Institute of Scientific and Technical Information of China (English)

    Wang Lei; Hui Yu; Gao Chaoqun; Jing Yupeng

    2011-01-01

    A novel wet vapor photoresist stripping technology is developed as an alternative to dry plasma ashing and wet stripping. Experiments using this technology to strip hard baked SU-8 photoresist, aurum and chromium film are carried out. Then the images of stripping results are shown and the mechanism is analyzed and discussed.The most striking result of this experiment is that the spraying mixture of steam and water droplets can strip photoresist and even metal film with ease.

  13. Regeneration of poly-L-lysine modified carbon electrodes in the accumulation and cathodic stripping voltammetric determination of the cromoglycate anion.

    Science.gov (United States)

    Pereira, F C; Fogg, A G; Zanoni, M V B

    2003-07-27

    Cromoglycate is accumulated on a poly-L-lysine (PLL) modified carbon electrode best from pH 4 solution, where it is anionic and the PLL is cationic, and at which pH the cromoglycate gives a good reduction peak at -0.82 V. The PLL film can be regenerated readily by washing the electrode with 3 M sodium hydroxide solution, in which the PLL is deprotonated. Regeneration of the film is not required as frequently when larger amounts of PLL are incorporated into it. This allows standard addition procedures to be carried out without regenerating the electrode. Linear calibration graphs have been obtained typically in the range 0.1-1.5 microg ml(-1). Detection limits have been calculated to be 10 ng ml(-1). The standard addition method has been applied satisfactorily to diluted urine solutions.

  14. The contents of sesamol and related lignans in sesame, tahina and halva as determined by a newly developed polarographic and stripping voltammetric analysis

    Energy Technology Data Exchange (ETDEWEB)

    Tokusoglu, O.; Kocak, S.; Aycan, S.

    2009-07-01

    The contents of antioxidant lignans (Sesamol) in sesame, commercial formulations of tahina and halva, which are processed tahina foods, were determined by Differential Pulse Polarography (DPP) with a capillary hanging mercury drop electrode (HMDE). A platinum wire was used as the counter electrode and Ag/AgCl was the reference electrode. Samples have been analyzed by standard addition procedures and found to be quantitative (p<0.01). Due to the fact that sesamol is an oil-soluble phenolic compound , it was found in the oil levels of sesame, tahina and halvas. Sesame samples contained 51.05-56.46 % in oil whereas tahina samples contained 52.12-53.79 % in oil. The oil percentage of plain halva was found to be 28.79 - 30.13 % (p<0.01). Phenolic lignans sesamol in sesame was 0.26-0.32 mg/100g oil, whereas the sesamol in tahina was 10.98-12.33 mg/100g oil. The sesamol in commercial plain halva samples and the open marketed plain halva samples contained 8.24-9.12 mg/100g oil and 4.97 mg sesamol /100g oil, respectively (R{sup 2}=0.9999) (p<0.01). The proposed Differential Pulse Polarographic (DPP) method is a rapid, reproducible procedure for the simultaneous determination of phenolic lignans in sesame and food products with sesame. It provides an adequate, sensitive, quantitative detection of these nutraceuticals in the commercial food industry. (Author) 26 refs.

  15. The contents of sesamol and related lignans in sesame, tahina and halva as determined by a newly developed polarographic and stripping voltammetric analysis

    Directory of Open Access Journals (Sweden)

    2009-06-01

    Full Text Available The contents of antioxidant lignans (Sesamol in sesame, commercial formulations of tahina and halva, which are processed tahina foods, were determined by Differential Pulse Polarography (DPP with a capillary hanging mercury drop electrode (HMDE. A platinum wire was used as the counter electrode and Ag/AgCl was the reference electrode. Samples have been analyzed by standard addition procedures and found to be quantitative (p2=0.9999 (pSe determinó el contenido del lignano antioxidante (Sesamol en sésamo, formulaciones comerciales de tahina y halva, que es el producto procesado de tahina, por polarografía de pulsos diferencial (DPP con un capilar conteniendo un electrodo de gota de mercurio (HMDE. Un hilo de platino fué usado como el electrodo contador y Ag/AgCl como electrodo de referencia. Las muestras fueron analizadas por procedimientos de adición de patrones y se encontró que wl procedimiento era cuantitativo (p2= 0.9999 (p< 0.01. El método polarográfico propuesto (DPP es un método rápido y reproducible para la determinación simultánea de lignanos fenólicos en sésamo y otros productos alimentarios que contienen sésamo. Éste proporciona una detección cuantitativa adecuada y sensible de este compuesto nutraceútico en alimentos comerciales.

  16. A self-polishing platinum ring voltammetric sensor and its application to complex media.

    Science.gov (United States)

    Cavanillas, Santiago; Winquist, Fredrik; Eriksson, Mats

    2015-02-15

    A self-polishing voltammetric sensor was recently developed and has been applied to samples of urea, milk and sewage water. The polishing device continuously grinds a platinum ring electrode, offering a reproducible and clean electrode surface. Principal component analysis (PCA) and partial least squares (PLS) techniques were applied to interpret the data and to build prediction models. In an evaluation of samples with different urea concentrations, the grinding step allows for repeatable measurements, similar to those after electrochemical cleaning. Furthermore, for the determination of sewage water concentrations in drinking water and for the evaluation of different fat contents in milk samples, the polishing eliminates sensor drift produced by electrode fouling. The results show that the application of a self-polishing unit offers a promising tool for electrochemical studies of difficult analytes and complex media. Copyright © 2014 Elsevier B.V. All rights reserved.

  17. Differential Pulse Voltammetric Determination of Fulvestrant in Pharmaceutical Dosage Forms and Serum Samples

    Directory of Open Access Journals (Sweden)

    Dilek Kul

    2011-01-01

    Full Text Available The electrooxidation behavior and determination of fulvestrant at a glassy carbon electrode were investigated. The voltammetric study of the model compounds allowed elucidating the possible oxidation mechanism of fulvestrant. The dependence of the peak current and peak potentials on pH, concentration, nature of the buffer, and scan rate was determined. The oxidation of fulvestrant showed a single and irreversible peak at glassy carbon electrode, and the process was found diffusion controlled. Linear responses were obtained for the concentrations between 4×10−6 M and 6×10−5 M in standard samples and between 2×10−5 M and 1×10−4 M in serum samples. The repeatability of the method was found 0.93 RSD%. The repeatability, reproducibility, precision, and accuracy of proposed method were investigated.

  18. Detection of Adulteration in Argan Oil by Using an Electronic Nose and a Voltammetric Electronic Tongue

    Directory of Open Access Journals (Sweden)

    Madiha Bougrini

    2014-01-01

    Full Text Available Adulteration detection of argan oil is one of the main aspects of its quality control. Following recent fraud scandals, it is mandatory to ensure product quality and customer protection. The aim of this study is to detect the percentages of adulteration of argan oil with sunflower oil by using the combination of a voltammetric e-tongue and an e-nose based on metal oxide semiconductor sensors and pattern recognition techniques. Data analysis is performed by three pattern recognition methods: principal component analysis (PCA, discriminant factor analysis (DFA, and support vector machines (SVMs. Excellent results were obtained in the differentiation between unadulterated and adulterated argan oil with sunflower one. To the best of our knowledge, this is the first attempt to demonstrate whether the combined e-nose and e-tongue technologies could be successfully applied to the detection of adulteration of argan oil.

  19. Rapid screening and guided extraction of antioxidants from microalgae using voltammetric methods.

    Science.gov (United States)

    Goiris, Koen; De Vreese, Peter; De Cooman, Luc; Muylaert, Koenraad

    2012-08-01

    Currently, microalgae draw much attention as a promising source of natural antioxidants to replace synthetic antioxidants for food applications. In this paper, the use of voltammetric techniques as a fast alternative for chemical assays to determine the antioxidant power of microalgal biomass is discussed. It was found that antioxidant activities determined by square wave voltammetry correlate well with the results from other established antioxidant assays, such as Trolox equivalent antioxidant capacity (R(2) = 0.737), ferric reducing antioxidant potential (R(2) = 0.729), and AAPH-induced oxidation of linoleic acid (R(2) = 0.566). Besides yielding quantitative data on the antioxidant activity, square wave voltammetry provides additional information on the antioxidant profile of microalgal biomass as the peak potentials of antioxidant components are determined. Consequently, square wave voltammetry can be used as a tool for optimizing the extraction processes to recover antioxidant components from microalgae.

  20. Spectrophotometric and Voltammetric Studies on the Interaction of Heparin with Phenosafranine

    Institute of Scientific and Technical Information of China (English)

    Wei SUN; Ya Qin DING; Kui JIAO

    2005-01-01

    The interaction of phenosafranine (PSF) with a glycosaminoglycans of heparin (Hep) in aqueous solution has been characterized by UV-Vis absorption spectrophotometry and cyclic voltammetry in pH 1.5 Britton-Robinson (B-R) buffer solution. The addition of Hep caused decrease of the absorbance of PSF at 532 nm and the redox peak current of PSF. The study showed that an supramolecular complex of PSF-Hep was formed because of the electrostatic attraction of negatively charged Hep with the positively charged PSF, which resulted in the decrease of the equilibrium concentration of PSF in solutions, and the decrease of the absorbance or the Peak current of PSF. The stoichiometry of the Hep/PSF complex was further calculated by voltammetric data with the result of 1:1 complex.

  1. Voltammetric Determination of Estrogens Based on the Enhancement Effect of Surfactant at Carbon Paste Electrode

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Highly sensitive voltammetric method for the determination of estrogens, based on the enhancement effect of cetyltrimethylammonium bromide (CTAB) has been described. In the presence of CTAB, the oxidation peak currents of estrogens (estradiol, estrone, estriol, estradiol valerate and diethylstilbestrol) at the carbon paste electrode (CPE) increased significantly after open-circuit accumulation. The peak current was proportional to the concentration of estradiol over the range from 5×10-9 to 2.5×10-6 mol\\5L-1. The detection limit was 8×10-10 mol\\5L-1 at 6 min of accumulation. The total amounts of estrogens in the blood serums were determined and the average recovery was 104.92%. Under the conditions used, the electrode process of estradiol was examined and the mechanism for peak current enhancement was also discussed.

  2. Detection of iron(III)-binding ligands originating from marine phytoplankton using cathodic stripping voltammetry.

    Science.gov (United States)

    Hasegawa, Hiroshi; Maki, Teruya; Asano, Kohnosuke; Ueda, Kentaro; Ueda, Kazumasa

    2004-01-01

    The sample preparation and analytical methodology are described for detecting biologically produced iron(III)-binding ligands in laboratory cultures of coastal marine phytoplankton. The iron(III)-binding ligands from the culture media were purified by passage through a column packing with a hydrophobic absorbent. The concentrations and stability constants of the ligands were determined by adsorptive cathodic stripping voltammetry with competitive ligand equilibration. The analytical results of the cultivated cultures suggest that eukaryotic phytoplankton would produce iron(III)-binding ligands in analogy with other microorganisms.

  3. Discrimination of Apple Liqueurs (Nalewka Using a Voltammetric Electronic Tongue, UV-Vis and Raman Spectroscopy

    Directory of Open Access Journals (Sweden)

    Magdalena Śliwińska

    2016-10-01

    Full Text Available The capability of a phthalocyanine-based voltammetric electronic tongue to analyze strong alcoholic beverages has been evaluated and compared with the performance of spectroscopic techniques coupled to chemometrics. Nalewka Polish liqueurs prepared from five apple varieties have been used as a model of strong liqueurs. Principal Component Analysis has demonstrated that the best discrimination between liqueurs prepared from different apple varieties is achieved using the e-tongue and UV-Vis spectroscopy. Raman spectra coupled to chemometrics have not been efficient in discriminating liqueurs. The calculated Euclidean distances and the k-Nearest Neighbors algorithm (kNN confirmed these results. The main advantage of the e-tongue is that, using PLS-1, good correlations have been found simultaneously with the phenolic content measured by the Folin–Ciocalteu method (R2 of 0.97 in calibration and R2 of 0.93 in validation and also with the density, a marker of the alcoholic content method (R2 of 0.93 in calibration and R2 of 0.88 in validation. UV-Vis coupled with chemometrics has shown good correlations only with the phenolic content (R2 of 0.99 in calibration and R2 of 0.99 in validation but correlations with the alcoholic content were low. Raman coupled with chemometrics has shown good correlations only with density (R2 of 0.96 in calibration and R2 of 0.85 in validation. In summary, from the three holistic methods evaluated to analyze strong alcoholic liqueurs, the voltammetric electronic tongue using phthalocyanines as sensing elements is superior to Raman or UV-Vis techniques because it shows an excellent discrimination capability and remarkable correlations with both antioxidant capacity and alcoholic content—the most important parameters to be measured in this type of liqueurs.

  4. Voltammetric Behaviour of Sulfamethoxazole on Electropolymerized-Molecularly Imprinted Overoxidized Polypyrrole

    Directory of Open Access Journals (Sweden)

    Yücel Sahin

    2008-12-01

    Full Text Available In this work, preparation of a molecularly imprinted polymer (MIP film and its recognition properties for sulfamethoxazolewere investigated. The overoxidized polypyrrole (OPPy film was prepared by the cyclic voltammetric deposition of pyrrole (Py in the presence of supporting electrolyte (tetrabutylammonium perchlorate-TBAP with and without a template molecule (sulfamethoxazole on a pencil graphite electrode (PGE. The voltammetric behaviour of sulfamethoxazole on imprinted and non-imprinted (NIP films was investigated by differential pulse voltammetry (DPV in Britton-Robinson (BR buffer solutions prepared in different ratio of acetonitrile-water binary mixture, between the pH 1.5 and 7.0. The effect of the acetonitrile-water ratio and pH, monomer and template concentrations, electropolymerization cycles on the performance of the MIP electrode was investigated and optimized. The MIP electrode exhibited the best reproducibility and highest sensitivity. The results showed that changing acetonitrile-water ratio and pH of BR buffer solution changes the oxidation peak current values. The highest anodic signal of sulfamethoxazole was obtained in BR buffer solution prepared in 50% (v/v acetonitrile-water at pH 2.5. The calibration curve for sulfamethoxazole at MIP electrode has linear region for a concentration range of 25.10-3 to 0.75 mM (R2=0.9993. The detection limit of sulfamethoxazole was found as 3.59.10-4 mM (S/N=3. The same method was also applied to determination of sulfamethoxazole in commercial pharmaceutical samples. Method precision (RSD87% were satisfactory. The proposed method is simple and quick. The polypyrrole (PPy electrodes have low response time, good mechanical stability and are disposable simple to construct.

  5. Discrimination of Apple Liqueurs (Nalewka) Using a Voltammetric Electronic Tongue, UV-Vis and Raman Spectroscopy.

    Science.gov (United States)

    Śliwińska, Magdalena; Garcia-Hernandez, Celia; Kościński, Mikołaj; Dymerski, Tomasz; Wardencki, Waldemar; Namieśnik, Jacek; Śliwińska-Bartkowiak, Małgorzata; Jurga, Stefan; Garcia-Cabezon, Cristina; Rodriguez-Mendez, Maria Luz

    2016-10-09

    The capability of a phthalocyanine-based voltammetric electronic tongue to analyze strong alcoholic beverages has been evaluated and compared with the performance of spectroscopic techniques coupled to chemometrics. Nalewka Polish liqueurs prepared from five apple varieties have been used as a model of strong liqueurs. Principal Component Analysis has demonstrated that the best discrimination between liqueurs prepared from different apple varieties is achieved using the e-tongue and UV-Vis spectroscopy. Raman spectra coupled to chemometrics have not been efficient in discriminating liqueurs. The calculated Euclidean distances and the k-Nearest Neighbors algorithm (kNN) confirmed these results. The main advantage of the e-tongue is that, using PLS-1, good correlations have been found simultaneously with the phenolic content measured by the Folin-Ciocalteu method (R² of 0.97 in calibration and R² of 0.93 in validation) and also with the density, a marker of the alcoholic content method (R² of 0.93 in calibration and R² of 0.88 in validation). UV-Vis coupled with chemometrics has shown good correlations only with the phenolic content (R² of 0.99 in calibration and R² of 0.99 in validation) but correlations with the alcoholic content were low. Raman coupled with chemometrics has shown good correlations only with density (R² of 0.96 in calibration and R² of 0.85 in validation). In summary, from the three holistic methods evaluated to analyze strong alcoholic liqueurs, the voltammetric electronic tongue using phthalocyanines as sensing elements is superior to Raman or UV-Vis techniques because it shows an excellent discrimination capability and remarkable correlations with both antioxidant capacity and alcoholic content-the most important parameters to be measured in this type of liqueurs.

  6. Structure sensitivity in adsorption

    DEFF Research Database (Denmark)

    Hammer, Bjørk; Nielsen, Ole Holm; Nørskov, Jens Kehlet

    1997-01-01

    The structure sensitivity of CO adsorption on different flat, stepped, kinked and reconstructed Pt surfaces is studied using large-scale density-functional calculations. We find an extremely strong structure sensitivity in the adsorption energy with variations up to 1 eV (or 100%) from one...

  7. A Simple Adsorption Experiment

    Science.gov (United States)

    Guirado, Gonzalo; Ayllon, Jose A.

    2011-01-01

    The study of adsorption phenomenon is one of the most relevant and traditional physical chemistry experiments performed by chemistry undergraduate students in laboratory courses. In this article, we describe an easy, inexpensive, and straightforward way to experimentally determine adsorption isotherms using pieces of filter paper as the adsorbent…

  8. Effect of Load Distribution on Strip Crown in Hot Strip Rolling

    Institute of Scientific and Technical Information of China (English)

    Hongshuang DI; Jianzhong XU; Dianyao GONG; Xianghua LIU; Guodong WANG; Xiaoming HE; Liying BA

    2004-01-01

    In order to establish precision model, a software to calculate the strip crown of four-high hot rolling mill was developed by using affecting function method according to the strip crown calculation theory. The effect of work roll diameter, unit width rolling load, roll bending force, work roll crown, initial strip crown and reduction, etc, on load distribution effect rate was simulated by using the software. The results show that the load distribution effect rate increases with the increase of strip width, work roll diameter, unit width rolling load, roll bending force, work roll crown, initial strip crown and reduction. Based on the simulation results, base value of load distribution effect rate and fitting coefficients of six power polynomial of load distribution effect rate modification coefficient were determined considering all of the above parameters. A simplified mathematical model for calculating load distribution effect rate was established.

  9. Anodic stripping voltammetry of silver nanoparticles: aggregation leads to incomplete stripping.

    Science.gov (United States)

    Cloake, Samantha J; Toh, Her Shuang; Lee, Patricia T; Salter, Chris; Johnston, Colin; Compton, Richard G

    2015-02-01

    The influence of nanoparticle aggregation on anodic stripping voltammetry is reported. Dopamine-capped silver nanoparticles were chosen as a model system, and melamine was used to induce aggregation in the nanoparticles. Through the anodic stripping of the silver nanoparticles that were aggregated to different extents, it was found that the peak area of the oxidative signal corresponding to the stripping of silver to silver(I) ions decreases with increasing aggregation. Aggregation causes incomplete stripping of the silver nanoparticles. Two possible mechanisms of 'partial oxidation' and 'inactivation' of the nanoparticles are proposed to account for this finding. Aggregation effects must be considered when anodic stripping voltammetry is used for nanoparticle detection and quantification. Hence, drop casting, which is known to lead to aggregation, is not encouraged for preparing electrodes for analytical purposes.

  10. Development of floating strip micromegas detectors

    Energy Technology Data Exchange (ETDEWEB)

    Bortfeldt, Jonathan

    2014-04-28

    Micromegas are high-rate capable, high-resolution micro-pattern gaseous detectors. Square meter sized resistive strip Micromegas are foreseen as replacement of the currently used precision tracking detectors in the Small Wheel, which is part of the forward region of the ATLAS muon spectrometer. The replacement is necessary to ensure tracking and triggering performance of the muon spectrometer after the luminosity increase of the Large Hadron Collider beyond its design value of 10{sup 34} cm{sup -2}s{sup -1} around 2020. In this thesis a novel discharge tolerant floating strip Micromegas detector is presented and described. By individually powering copper anode strips, the effects of a discharge are confined to a small region of the detector. This reduces the impact of discharges on the efficiency by three orders of magnitude, compared to a standard Micromegas. The physics of the detector is studied and discussed in detail. Several detectors are developed: A 6.4 x 6.4 cm{sup 2} floating strip Micromegas with exchangeable SMD capacitors and resistors allows for an optimization of the floating strip principle. The discharge behavior is investigated on this device in depth. The microscopic structure of discharges is quantitatively explained by a detailed detector simulation. A 48 x 50 cm{sup 2} floating strip Micromegas is studied in high energy pion beams. Its homogeneity with respect to pulse height, efficiency and spatial resolution is investigated. The good performance in high-rate background environments is demonstrated in cosmic muon tracking measurements with a 6.4 x 6.4 cm{sup 2} floating strip Micromegas under lateral irradiation with 550 kHz 20 MeV proton beams. A floating strip Micromegas doublet with low material budget is developed for ion tracking without limitations from multiple scattering in imaging applications during medical ion therapy. Highly efficient tracking of 20 MeV protons at particle rates of 550 kHz is possible. The reconstruction of the

  11. Area specific stripping factors for AGS. A method for extracting stripping factors from survey data

    Energy Technology Data Exchange (ETDEWEB)

    Aage, H.K.; Korsbech, U. [Technical Univ. of Denmark (Denmark)

    2006-04-15

    In order to use Airborne Gamma-ray Spectrometry (AGS) for contamination mapping, for source search etc. one must to be able to eliminate the contribution to the spectra from natural radioactivity. This in general is done by a stripping technique. The parameters for performing a stripping have until recently been measured by recording gamma spectra at special calibration sites (pads). This may be cumbersome and the parameters may not be correct when used at low gamma energies for environmental spectra. During 2000-2001 DTU tested with success a new technique for Carborne Gamma-ray Spectrometry (CGS) where the spectra from the surveyed area (or from a similar area) were used for calculating the stripping parameters. It was possible to calculate usable stripping ratios for a number of low energy windows - and weak source signals not detectable by other means were discovered with the ASS technique. In this report it is shown that the ASS technique also works for AGS data, and it has been used for recent Danish AGS tests with point sources. (Check of calibration of AGS parameters.) By using the ASS technique with the Boden data (Barents Rescue) an exercise source was detected that has not been detected by any of the teams during the exercise. The ASS technique therefore seems to be better for search for radiation anomalies than any other method known presently. The experiences also tell that although the stripping can be performed correctly at any altitude there is a variation of the stripping parameters with altitude that has not yet been quite understood. However, even with the oddly variations the stripping worked as expected. It was also observed that one might calculate a single common set of usable stripping factors for all altitudes from the entire data set i.e. some average a, b and c values. When those stripping factors were used the stripping technique still worked well. (au)

  12. Modeling of continuous strip production by rheocasting

    Science.gov (United States)

    Matsumiya, T.; Flemings, M. C.

    1981-03-01

    A process was experimentally and mathematically modeled for continuous and direct production of metal strip from its molten state by the use of Rheocasting. The process comprises 1) continuous production of a Rheocast semisolid alloy, and 2) direct shaping of the semisolid into strip. Sn-15 pct Pb was used as the modeling alloy. Crack formation and surface quality of the strip produced depend on fraction solid and deformation force. Continuous, sound strip could be obtained with good surface quality when fraction solid was between 0.50 and 0.70 and deformation force did not exceed a given maximum. Sheet thickness depends on deformation force, fraction solid, rotor rate of Rheocaster and production line speed. At constant deformation force, sheet thickness increases as fraction solid increases, rotor rate decreases and line speed is reduced. Sheet thickness is larger in the center than in the edge, but the difference is reduced by applying edgers. Some segregation of lead toward the edges is observed, and the segregation increases as amount of deformation is increased. A mathematical model for heat flow, solidification and deformation was constructed. The model predicts the point of completion of solidification in the strip and sheet thickness as a function of deformation force and line speed. Calculations are in good agreement with experimental results.

  13. Modeling of continuous strip production by rheocasting

    Energy Technology Data Exchange (ETDEWEB)

    Matsumiya, T.; Flemings, M.C.

    1981-03-01

    A process was experimentally and mathematically modeled for continuous and direct production of metal strip from its molten state by the use of Rheocasting. The process comprises 1) continuous production of a Rheocast semisolid alloy, and 2) direct shaping of the semisolid into strip. Sn-15 pct Pb was used as the modeling alloy. Crack formation and surface quality of the strip produced depend on fraction solid and deformation force. Continuous, sound strip could be obtained with good surface quality when fraction solid was between 0.50 and 0.70 and deformation force did not exceed a given maximum. Sheet thickness depends on deformation force, fraction solid, rotor rate of Rheocaster and production line speed. At constant deformation force, sheet thickness increases as fraction solid increases, rotor rate decreases and line speed is reduced. Sheet thickness is larger in the center than in the edge, but the difference is reduced by applying edgers. Some segregation of lead toward the edges is observed, ad the segregation increases as amount of deformation is increased. A mathematical model for heat flow, solidification and deformation was constructed. The model predicts the point of completion of solidification in the strip and sheet thickness as a function of deformation force and line speed. Calculations are in good agreement with experimental results.

  14. Beam stripping extraction from the VINCY cyclotron

    Directory of Open Access Journals (Sweden)

    Ristić-Đurović Jasna L.

    2006-01-01

    Full Text Available The extraction system of a cyclotron guides an ion beam from a spiral acceleration orbit, through an extraction trajectory, into a high energy transport line. The two methods commonly used to direct an ion into the extraction path are deflection, by the electric field of an electrostatic deflector, and ion stripping, by a thin carbon foil. Compared to the electrostatic deflector system, the stripping extraction provides a fast and easy change of the extracted ion energy and is easier to manufacture operate, and maintain. However, the extraction trajectory and dynamics of an ion beam after stripping are highly dependant on the ion energy and specific charge. Thus, when a multipurpose machine such as the VINCY Cyclotron is concerned, it is far from easy to deliver a variety of ion beams into the same high energy transport line and at the same time preserve a reasonable compactness of the extraction system. The front side stripping extraction system of the VINCY Cyclotron provides high (~70 MeV and mid (~30 MeV energy protons, as well as a number of heavy ions in broad energy ranges. The back side stripping extraction system extracts low energy protons (~18 MeV and enables their simultaneous use with high energy protons at the front side of the machine.

  15. Effect of Initial Crown on Shape of Hot Rolled Strip

    Institute of Scientific and Technical Information of China (English)

    HU Yu; GONG Dian-yao; JIANG Zheng-yi; XU Jian-zhong; ZHANG Dian-hua; LIU Xiang-hua

    2009-01-01

    Based on the influence coefficient method, the effect of entry strip crown on the shape of hot rolled strip was analyzed using the software of roll elastic deformation simulation. According to the practical condition of a domestic hot roiled strip plant, the unit strip crown change from the first stand to the last stand was calculated when the entry crown of hot strip varies. The calculated result shows that the entry strip crown does not significantly affect the target strip crown at the exit of the last finishing stand in respect to a fixed strip shape control reference (such as bending force). The calculation was analyzed, and the research is helpful in modeling strip shape setup and shape control.

  16. An electroanalytical approach for evaluation of biochar adsorption characteristics and its application for lead and cadmium determination.

    Science.gov (United States)

    Suguihiro, Talita Mayumi; de Oliveira, Paulo Roberto; de Rezende, Edivaltrys Inayve Pissinati; Mangrich, Antonio Sálvio; Marcolino, Luiz Humberto; Bergamini, Márcio F

    2013-09-01

    This work describes for first time the use of electroanalytical techniques for evaluation of adsorptive proprieties of biochar using it as electrode modifier and its application for preconcentration and determination of Lead(II) and Cadmium(II) under differential pulse adsorptive voltammetric conditions (DPAdSV). Samples of biochars were obtained from castor oil cake using a predefined set of experimental conditions varying the heating rate (V), final temperature (T) and warm-up period (P) and subsequently used for carbon paste modified electrode (CPME) preparation. The proposed method was applied for Lead(II) and Cadmium(II) determination in spiked simulated industrial effluents and the limit of detection obtained for both metals were adequated for determination of these evaluated ions taking into account the limits established by Brazilian legislation. For all samples analyzed, recoveries ranged from 95% to 104% were obtained and no significative interferences were observed for common cations in water samples.

  17. Ram pressure stripping of tilted galaxies

    CERN Document Server

    Jachym, P; Palous, J; Combes, F

    2009-01-01

    Ram pressure stripping of galaxies in clusters can yield gas deficient disks. Previous numerical simulations based on various approaches suggested that, except for near edge-on disk orientations, the amount of stripping depends very little on the inclination angle. Following our previous study of face-on stripping, we extend the set of parameters with the disk tilt angle and explore in detail the effects of the ram pressure on the interstellar content (ISM) of tilted galaxies that orbit in various environments of clusters, with compact or extended distributions of the intra-cluster medium (ICM). We further study how results of numerical simulations could be estimated analytically. A grid of numerical simulations with varying parameters is produced using the tree/SPH code GADGET with a modified method for calculating the ISM-ICM interaction. These SPH calculations extend the set of existing results obtained from different codes using various numerical techniques. The simulations confirm the general trend of le...

  18. Asset Stripping in a Mature Market Economy

    DEFF Research Database (Denmark)

    Klarskov Jeppesen, Kim; Møller, Ulrik Gorm

    2011-01-01

    indicates that asset stripping may take place in mature market economies to the extent that perpetrators are able to circumvent the corporate governance system by giving lawyers, public accountants and banks incentives to act less critically towards dubious business transactions. Research limitations......Purpose – The purpose of this paper is to document a Danish fraud scheme, in which a large number of limited companies were stripped of their assets leaving them with nothing but tax debt, eventually causing the Danish Tax and Customs Administration to lose large sums. Furthermore, the purpose...... is to analyse why the asset-stripping schemes occurred in a mature market economy with a strong corporate governance system and a low level of corruption. Design/methodology/approach – The research is conducted as a longitudinal single case study based on documentary research. Findings – The Danish case...

  19. Rapid diagnosis of meningitis using reagent strips

    Directory of Open Access Journals (Sweden)

    Parmar Ramesh

    2004-02-01

    Full Text Available OBJECTIVES: Identification of causative agent with estimation of cerebrospinal fluid (CSF glucose, protein, cells is necessary for accurate diagnosis of meningitis. Unfortunately, even these facilities are not available in many areas. Reagent strips that measure glucose and protein in blood and urine can serve this task but have been used with varying results in the past. This study was carried out to evaluate the utility and efficacy of Combur 10 strips in the diagnosis of meningitis. DESIGN, SETTINGS AND METHODS: A prospective clinical single blinded study of 63 children suspected to have meningitis undergoing CSF analysis. Each CSF sample was divided in to two and was utilised for reagent strip analysis in addition to standard laboratory evaluation and a correlation analysis were made. Statistical Method used: Results were analysed using standard statistical tests. Accuracy of the reagent strips as a screening tool was established using Godyn′s test. RESULTS: The sensitivity, specificity of the reagent strips for the diagnosis of meningitis was 97.14%, 96.42%. The sensitivity, specificity for tuberculous meningitis and bacterial meningitis were 100%, and 96.55%. That for the aseptic meningitis was 70% and 96.55%. Accuracy for the diagnosis of meningitis as a whole, bacterial meningitis, tuberculous meningitis, and aseptic meningitis were 96.78%, 98.2%, 98.27% and 83.0% respectively. CONCLUSION: Combur10 strips thus can be used for the rapid CSF analysis and screening with good accuracy. In situations where facilities of routine laboratory testing are not available this can be of an immense help.

  20. Removal of Trichloroethylene from Water by Adsorption on to Multiwall Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    S. Nasseri

    2011-10-01

    Full Text Available Groundwater recourses may be contaminated with trichloroethylene (TCE which is used in electronic, electric, dry cleaning and other similar industries and often treated by air stripping, which TCE in its vapor form is stripped from groundwater by air and is emitted into the atmosphere without any additional treatments. Carbon nanotubes are expected to play an important role in sensing, pollution treatment and separation techniques. In this study adsorption of trichloroethylene on multiwall carbon nanotubes has been investigated. The effect of contact time, pH, initial concentration of trichloroethylene and temperature on its adsorption were investigated. Adsorption isotherms and related constants were also determined. Results showed that contact times to reach equilibrium changed from 30 min (for 150 μg/L initial concentration to 10 min (for 600 μg/L concentrations at 25 °C; the equilibrium times in 40°C were 40 min and 15 min, respectively. Multi-wall carbon nanotubes showed to act as a good adsorbent for TCE in a wide range of pH=(3-9. For pH>9, adsorption decreased due to ionization of oxygen-containing groups. Adsorption test results revealed that TCE adsorption on the studied adsorbents could be better described by Freundlich isotherm.

  1. Lubrication in strip cold rolling process

    Institute of Scientific and Technical Information of China (English)

    Jianlin Sun; Yonglin Kang; Tianguo Xiao; Jianze Wang

    2004-01-01

    A lubrication model was developed for explaining how to form an oil film in the deformation zone, predicting the film thickness and determining the characteristics of lubrication in the strip rolling process, combined with the knowledge of hydrodythicknesses in the strip cold rolling. Results from the experiment and calculation show that the oil film forming in hydrodynamic lubrication is up to the bit angle and a higher rolling speed or a higher rolling oil viscosity. The mechanism of mechanical entrainment always affects the film thickness that increases with the rolling oil viscosity increasing or the reduction rate decreasing in rolling.

  2. Potential profile in a conducting polymer strip

    DEFF Research Database (Denmark)

    Bay, Lasse; West, Keld; Vlachopoulos, Nikolaos

    2002-01-01

    and complicate measurements on free-standing films. A model of the potential profile in a free-standing strip is derived. It is found that the active length (the length with a given potential change) of the polymer will scale as square root (d sigma /i/sub d/). (d is the thickness, sigma the conductivity...... of the film, and i/sub d/ the diffusion limited current density for oxygen reduction). The active length is typically of the order of millimeters. The model is compared with measurements on a strip of polypyrrole doped with dodecylbenzene sulfonate...

  3. Validation of the Hot Strip Mill Model

    Energy Technology Data Exchange (ETDEWEB)

    Richard Shulkosky; David Rosberg; Jerrud Chapman

    2005-03-30

    The Hot Strip Mill Model (HSMM) is an off-line, PC based software originally developed by the University of British Columbia (UBC) and the National Institute of Standards and Technology (NIST) under the AISI/DOE Advanced Process Control Program. The HSMM was developed to predict the temperatures, deformations, microstructure evolution and mechanical properties of steel strip or plate rolled in a hot mill. INTEG process group inc. undertook the current task of enhancing and validating the technology. With the support of 5 North American steel producers, INTEG process group tested and validated the model using actual operating data from the steel plants and enhanced the model to improve prediction results.

  4. Multi-twist optical Mobius strips

    CERN Document Server

    Freund, Isaac

    2009-01-01

    Circularly polarized Gauss-Laguerre GL(0,0) and GL(0,1) laser beams that cross at their waists at a small angle are shown to generate a quasi-paraxial field that contains an axial line of circular polarization, a C line, surrounded by polarization ellipses whose major and minor axes generate multi-twist Mobius strips with twist numbers that increase with distance from the C point. These Mobius strips are interpreted in terms of Berry's phase for parallel transport of the ellipse axes around the C point.

  5. slice of LEP beamtube with getter strip

    CERN Multimedia

    1989-01-01

    A section of the LEP beam pipe. This is the chamber in which LEP's counter-rotating electron and positron beams travel. It is made of lead-clad aluminium. The beams circulate in the oval cross-section part of the chamber. In the rectangular cross-section part, LEP's innovative getter-strip vacuum pump is installed. After heating to purify the surface of the getter, the strip acts like molecular sticky tape, trapping any stray molecules left behind after the accelerator's traditional vacuum pumps have done their job.

  6. Wokker. Notes on a Surrealist comic strip

    Directory of Open Access Journals (Sweden)

    Roger Sabin

    2012-05-01

    Full Text Available This essay explores the creation and development of a British comic strip, Wokker (1971-1999, and its connections with the surrealist movement. Although the strip is remarkable for its content and formalist properties, it remains obscure both because of its publishing circumstances, and because it does not fit easily into a history of comics. Rather it can be argued that its conceptual roots can be traced to the artistic ferment that happened in Paris in the 1920s (with Breton as a key reference point, and that it represents a very English, and late-flowering, example of the surrealist idea.

  7. Stage- vs. Channel-strip Metaphor

    DEFF Research Database (Denmark)

    Gelineck, Steven; Korsgaard, Dannie Michael; Büchert, Morten

    2015-01-01

    This study compares the stage metaphor and the channel strip metaphor in terms of performance. Traditionally, music mixing consoles employ a channels strip control metaphor for adjusting parameters such as volume and panning of each track. An alternative control metaphor, the so-called stage...... metaphor lets the user adjust volume and panning by positioning tracks relative to a virtual listening position. In this study test participants are given the task to adjust volume and panning of one channel (in mixes consisting of three channels) in order to replicate a series of simple pre-rendered mixes...

  8. Competitive Protein Adsorption - Multilayer Adsorption and Surface Induced Protein Aggregation

    DEFF Research Database (Denmark)

    Holmberg, Maria; Hou, Xiaolin

    2009-01-01

    In this study, competitive adsorption of albumin and IgG (immunoglobulin G) from human serum solutions and protein mixtures onto polymer surfaces is studied by means of radioactive labeling. By using two different radiolabels (125I and 131I), albumin and IgG adsorption to polymer surfaces...... is monitored simultaneously and the influence from the presence of other human serum proteins on albumin and IgG adsorption, as well as their mutual influence during adsorption processes, is investigated. Exploring protein adsorption by combining analysis of competitive adsorption from complex solutions...... of high concentration with investigation of single protein adsorption and interdependent adsorption between two specific proteins enables us to map protein adsorption sequences during competitive protein adsorption. Our study shows that proteins can adsorb in a multilayer fashion onto the polymer surfaces...

  9. Application of voltammetric techniques at microelectrodes to the study of the chemical stability of highly reactive species.

    Science.gov (United States)

    Laborda, Eduardo; Olmos, José-Manuel; Torralba, Encarnación; Molina, Angela

    2015-02-03

    The application of voltammetric techniques to the study of chemical speciation and stability is addressed both theoretically and experimentally in this work. In such systems, electrode reactions are coupled to homogeneous chemical equilibria (complexations, protonations, ion associations, ...) that can be studied in a simple, economical, and accurate way by means of electrochemical methods. These are of particular interest when some of the participating species are unstable given that the generation and characterization of the species are performed in situ and on a short time scale. With the above aim, simple explicit solutions are presented in this article for quantitative characterization with any voltammetric technique and with the most common electrode geometries. From the theoretical results obtained, it is pointed out that the use of square-wave voltammetry in combination with microelectrodes is very suitable. Finally, the theory is applied to the investigation of the ion association between the anthraquinone radical monoanion and the tetrabutylammonium cation in acetonitrile medium.

  10. Selective Voltammetric Determination of Uric Acid in the Presence of Ascorbic Acid at Ordered Mesoporous Carbon Modified Electrodes

    Institute of Scientific and Technical Information of China (English)

    WEN,Yan-Li; JIA,Neng-Qin; WANG,Zhi-Yong; SHEN,He-Bai

    2008-01-01

    A novel chemically modified electrode was fabricated by immobilizing ordered mesoporous carbon (OMC)onto a glassy carbon (GC) electrode.The electrocatalytic behavior of the OMC modified electrode towards the oxidation of uric acid (UA) and ascorbic acid (AA) was studied.Compared to a glassy carbon electrode,the OMC modified electrode showed a faster electron transfer rate and reduced the overpotentials greatly.Furthermore,the OMC modified electrode resolved the overlapping voltammetric responses of UA and AA into two well-defined voltammetric peaks with peak separation of ca.0.38 V.All results show that the OMC modified electrode has a good electrocatalytic ability to UA and AA,and has an excellent response towards UA even in the presence of high concentration AA.

  11. Influence of melatonin or its antagonism on alcohol consumption in ethanol drinking rats: a behavioral and in vivo voltammetric study.

    Science.gov (United States)

    Crespi, Francesco

    2012-05-03

    Melatonin, an indoleamine hormone synthesized in the pinealocytes, has been implicated as influencing the intake of alcohol in rats. It has been shown that this hormone is voltammetrically electroactive at the surface of pretreated carbon fiber microelectrodes in vitro and in vivo, in rat cerebral melatonergic regions such the pineal gland. The aim of this work consisted in the study of the influence of melatonin on spontaneously ethanol drinking or ethanol avoiding rats selected throughout a free choice two bottle test. It appeared that only the water preferring rats were affected by treatment with the hormone and that in vivo voltammetric related levels of melatonin were higher in the pineal gland of ethanol drinking rats versus water preferring rats. In addition, when treated with the melatonin antagonist GR128107 ethanol drinking rats significantly reduced the spontaneous consumption of alcohol.

  12. Voltammetric Study and Determination of Phenylephrine Hydrochloride at INP-Nafion-Modified CPE Sensor Employing Differential Pulse Voltammetry

    Directory of Open Access Journals (Sweden)

    Zeinab Pourghobadi

    2014-03-01

    Full Text Available In this study, describes the voltammetric oxidation and determination of phenylephrine (PHE hydrochloride at a new chemically modified electrode. Iron nanoparticle (INPs was dispersed in Nafion solution to obtain a INP-Nafion-modified CPE for the voltammetric analysis of PHE .The electrochemical behaviour of PHE on INP-Nafion-modified CPE was studied, using cyclic voltammetry as a diagnostic technique. The effects of amount of INPs-Nafion dispersion, pH, and scan rate on the response of modified electrode for the oxidation of PHE were investigated. Using differential pulse voltammetry (DPV, the modified electrode indicated a dynamic linear range for quantitative determination of PHE in the range of 5 μM−130 μM, and the detection limit was estimated to be 0.76 μM. The method was developed for the determination of PHE in pharmaceutical samples with satisfactory results.

  13. Investigation of voltammetric enzyme-linked immunoassay based on new system of ODA-H2O2-HRP

    Institute of Scientific and Technical Information of China (English)

    焦奎; 张书圣; 韦璐

    1996-01-01

    A voltammetric enzyme-linked immunoassay based on a new system of ODA-H2O2-HRP has first been developed and used in the detection of HRP and labelled HRP. By this method, the enzyme-catalyzing reaction of H2O2 oxidizing odianisidine (ODA) couples the electrode-reduction reaction of the oxidizing product of odianisidine, which produces a sensitive polarographic wave at potential of -0.56V (SCE) in Britton-Robinson buffer solution. In using this polarographic wave, a detection limit to HRP is 3.7×10-12g/mL and a linear range 1.0×10-11-2.0×10-9g/mL. And the mechanisms of the coupling reaction and the process of electro-reduction in the ODA-H2O2-HRP voltammetric enzyme-linked immunoassay system have also been carefully studied.

  14. Investigation of Mercury Reduction in Gold Stripping Process at Elevated Temperature

    Science.gov (United States)

    Pramudya, Irawan

    Mercury is present in many gold ores. By processing these ores, there is a potential of emitting mercury to the environment. Carbon regeneration kiln stacks have been observed as one of the primary source of mercury emission into the atmosphere. Before it is recycled back into the carbon in leach (CIL) or carbon in columns (CIC), carbon used in the gold extraction process needs to be reactivated thermally. Emission of mercury can be minimized by keeping the mercury left in the carbon low before it goes to the carbon regeneration kiln stacks. The objective of this study is establishing the optimum elution conditions of mercury cyanide from loaded carbon (which includes the eluent, concentration, temperature and elution time) with respect to gold stripping. Several methods such as acid washing (UNR-100, HCl or ethanol/UNR-100) were investigated prior to the stripping process. Furthermore, conventional pressurized Zadra and modified Zadra were also studied with regards to mercury concentration in the solution and vapor state as well as maximizing the gold stripping from industrial loaded carbon. 7% UNR-100 acid washing of loaded carbon at 80°C was able to wash out approximately 90% of mercury while maintaining the gold adsorption on the carbon (selective washing). The addition of alcohol in the UNR-100 acid washing solution was able to enhance mercury washing from 90% to 97%. Furthermore, mercury stripping using conventional pressurized (cyanide-alkaline) Zadra was best performed at 80°C (minimal amount of mercury reduced and volatilized) whereas using the same process only 40% of gold was stripped, which makes this process not viable. When alcohol was added to the stripping solution, at 80°C, 95% of gold was detected in the solution while keeping the reduction and volatilization of mercury low. The outcome of this study provides a better understanding of mercury behavior during the acid washing and stripping processes so that the risk of mercury exposure and

  15. Non-conductive nanomaterial enhanced electrochemical response in stripping voltammetry: The use of nanostructured magnesium silicate hollow spheres for heavy metal ions detection.

    Science.gov (United States)

    Xu, Ren-Xia; Yu, Xin-Yao; Gao, Chao; Jiang, Yu-Jing; Han, Dong-Dong; Liu, Jin-Huai; Huang, Xing-Jiu

    2013-08-06

    Nanostructured magnesium silicate hollow spheres, one kind of non-conductive nanomaterials, were used in heavy metal ions (HMIs) detection with enhanced performance for the first time. The detailed study of the enhancing electrochemical response in stripping voltammetry for simultaneous detection of ultratrace Cd(2+), Pb(2+), Cu(2+) and Hg(2+) was described. Electrochemical properties of modified electrodes were characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The operational parameters which have influence on the deposition and stripping of metal ions, such as supporting electrolytes, pH value, and deposition time were carefully studied. The anodic stripping voltammetric performance toward HMIs was evaluated using square wave anodic stripping voltammetry (SWASV) analysis. The detection limits achieved (0.186nM, 0.247nM, 0.169nM and 0.375nM for Cd(2+), Pb(2+), Cu(2+) and Hg(2+)) are much lower than the guideline values in drinking water given by the World Health Organization (WHO). In addition, the interference and stability of the modified electrode were also investigated under the optimized conditions. An interesting phenomenon of mutual interference between different metal ions was observed. Most importantly, the sensitivity of Pb(2+) increased in the presence of certain concentrations of other metal ions, such as Cd(2+), Cu(2+) and Hg(2+) both individually and simultaneously. The proposed electrochemical sensing method is thus expected to open new opportunities to broaden the use of SWASV in analysis for detecting HMIs in the environment. Copyright © 2013 Elsevier B.V. All rights reserved.

  16. A Rapid and Sensitive Diagnosis of Typhoid Fever Based On Nested PCR-Voltammetric DNA Biosensor Using Flagellin Gene Fragment

    Directory of Open Access Journals (Sweden)

    Yeni Wahyuni Hartati

    2016-03-01

    Full Text Available Typhoid fever caused by Salmonella typhi is an important issue for public health in the world. Laboratory methods for rapid and sensitive diagnosis are very important for disease management. The purpose of this study was to determine the performance of nested PCR–voltammetric DNA biosensor using flagellin gene (fla of S. typhi as a marker. The differential pulse voltammetry using pencil graphite electrode was applied to measure the guanine oxidation signal of probes vs synthetic target stDNA and probes vs fla PCR product hybridizations. The probe DNA selectivity was examined by hybridized probes vs non-complementary sequence. The result showed that the first round nested PCR product can not be visualized by agarose electrophoresis, whereas using the voltammetric biosensor methods can be detected both for the first or second round nested PCR product. The average peak current of hybridized probe vs first and second round of PCR product was 2.32 and 1.47 μA respectively, at 0.9 V. Detection of the DNA sequences of the infectious diseases from PCR amplified real sample was also carried out using this voltammetric DNA biosensor methods.

  17. Utility of Activated Glassy Carbon and Pencil Graphite Electrodes for Voltammetric Determination of Nalbuphine Hydrochloride in Pharmaceutical and Biological Fluids

    Directory of Open Access Journals (Sweden)

    Hoda M. Elqudaby

    2016-01-01

    Full Text Available This work compares voltammetric response of nalbuphine hydrochloride (NP·HCl at both activated glassy carbon and pencil graphite electrodes. The electrochemical oxidation of the drug was studied using cyclic voltammetry (CV, differential pulse voltammetry (DPV, and square wave voltammetry (SWV techniques. For analytical purpose a well-resolved irreversible diffusion controlled voltammetric peak was established in Britton-Robinson (B-R buffer solution of pH 6.00 using pencil graphite electrode (PGE. Using activated glassy carbon electrode (GCE a well-resolved irreversible diffusion controlled voltammetric peak was obtained at pH 7.00 using the same buffer solution. According to the linear relationship between the peak current and NP·HCl concentration, DPV and SWV methods were developed for their quantitative determination in pharmaceutical and human biological fluids. The linear response was obtained in the range from 1.6×10-5 to 1.5×10-4 mol L−1 using PGE and from 12.5×10-6 to 13.75×10-5 mol L−1 using a GC electrode, respectively. Precision and accuracy of the developed method were checked by recovery studies.

  18. Spectrometric and Voltammetric Analysis of Urease – Nickel Nanoelectrode as an Electrochemical Sensor

    Directory of Open Access Journals (Sweden)

    Rene Kizek

    2007-07-01

    Full Text Available Urease is the enzyme catalyzing the hydrolysis of urea into carbon dioxide andammonia. This enzyme is substrate-specific, which means that the enzyme catalyzes thehydrolysis of urea only. This feature is a basic diagnostic criterion used in thedetermination of many bacteria species. Most of the methods utilized for detection ofurease are based on analysis of its enzyme activity – the hydrolysis of urea. The aim of thiswork was to detect urease indirectly by spectrometric method and directly by voltammetricmethods. As spectrometric method we used is called indophenol assay. The sensitivity ofdetection itself is not sufficient to analyse the samples without pre-concentration steps.Therefore we utilized adsorptive transfer stripping technique coupled with differential pulse voltammetry to detect urease. The influence of accumulation time, pH of supporting electrolyte and concentration of urease on the enzyme peak height was investigated. Under the optimized experimental conditions (0.2 M acetate buffer pH 4.6 and accumulation time of 120 s the detection limit of urease evaluated as 3 S/N was 200 ng/ml. The activity of urease enzyme depends on the presence of nickel. Thus the influence of nickel(II ions on electrochemical response of the enzyme was studied. Based on the results obtained the interaction of nickel(II ions and urease can be determined using electrochemical methods. Therefore we prepared Ni nanoelectrodes to measure urease. The Ni nanoelectrodes was analysed after the template dissolution by scanning electron microscopy. The results shown vertically aligned Ni nanopillars almost covered the electrode surface, whereas the defect places are minor and insignificant in comparison with total electrode surface. We were able to not only detect urease itself but also to distinguish its native and denatured form.

  19. Hybrid adsorptive membrane reactor

    Science.gov (United States)

    Tsotsis, Theodore T. (Inventor); Sahimi, Muhammad (Inventor); Fayyaz-Najafi, Babak (Inventor); Harale, Aadesh (Inventor); Park, Byoung-Gi (Inventor); Liu, Paul K. T. (Inventor)

    2011-01-01

    A hybrid adsorbent-membrane reactor in which the chemical reaction, membrane separation, and product adsorption are coupled. Also disclosed are a dual-reactor apparatus and a process using the reactor or the apparatus.

  20. Hybrid adsorptive membrane reactor

    Science.gov (United States)

    Tsotsis, Theodore T.; Sahimi, Muhammad; Fayyaz-Najafi, Babak; Harale, Aadesh; Park, Byoung-Gi; Liu, Paul K. T.

    2011-03-01

    A hybrid adsorbent-membrane reactor in which the chemical reaction, membrane separation, and product adsorption are coupled. Also disclosed are a dual-reactor apparatus and a process using the reactor or the apparatus.

  1. Butanol production from wood pulping hydrolysate in an integrated fermentation-gas stripping process

    Energy Technology Data Exchange (ETDEWEB)

    Lu, CC; Dong, J; Yang, ST

    2013-09-01

    Wood pulping hydrolysate (WPH) containing mainly xylose and glucose as a potential substrate for acetone-butanol-ethanol (ABE) fermentation was studied. Due to the inhibitors present in the hydrolysate, several dilution levels and detoxification treatments, including overliming, activated charcoal adsorption, and resin adsorption, were evaluated for their effectiveness in relieving the inhibition on fermentation. Detoxification using resin and evaporation was found to be the most effective method in reducing the toxicity of WPH. ABE production in batch fermentation by Clostridium beijerinckii increased 68%, from 6.73 g/L in the non-treated and non-diluted WPH to 11.35 g/L in the resin treated WPH. With gas stripping for in situ product removal, ABE production from WPH increased to 17.73 g/L, demonstrating that gas stripping was effective in alleviating butanol toxicity by selectively separating butanol from the fermentation broth, which greatly improved solvents production and sugar conversion in the fermentation. (C) 2013 Elsevier Ltd. All rights reserved.

  2. Comparative evaluation of scanned stripping techniques: SSCP vs. SSV

    NARCIS (Netherlands)

    Town, R.M.; Leeuwen, van H.P.

    2006-01-01

    The characteristic features of scanned deposition potential curves constructed from stripping chronopotentiometry (SSCP) and various modes of stripping voltammetry (SSV) are critically evaluated. The strengths and weaknesses of each method for identification of metal ion speciation features and susc

  3. Topics in Chemical Instrumentation: CII. Automated Anodic Stripping Voltammetry.

    Science.gov (United States)

    Stock, John T.; Ewing, Galen W., Ed.

    1980-01-01

    Presents details of anodic stripping analysis (ASV) in college chemistry laboratory experiments. Provides block diagrams of the analyzer system, circuitry and power supplies of the automated stripping analyzer, and instructions for implementing microcomputer control of the ASV. (CS)

  4. Propulsion by Helical Strips in Circular Channels

    Science.gov (United States)

    Yesilyurt, Serhat; Demir, Ebru

    2016-11-01

    Progress in manufacturing techniques avails the production of artificial micro swimmers (AMS) in various shapes and sizes. There are numerous studies on the generation of efficient locomotion by means of helical tails with circular cross-sections. This work focuses on locomotion with helical strips in circular channels. A CFD model is used to analyze the effects of geometric parameters and the radius of the channel on swimming velocity of infinite helical-strips in circular channels. Results show that there is an optimum wavelength that depends on thickness to channel radius ratio, suggesting that these parameters need to be optimized simultaneously. With constant torque, thinner strips swim faster, whereas under constant angular velocity application, thicker strips (in radial direction) prevail. As width approaches the wavelength, velocity decreases under both conditions, unless a magnetically coated tail is simulated, for which width has an optimum value. Increasing channel radius to helix amplitude ratio increases the velocity up to a maximum and after a slight drop, saturation occurs as bulk swimming conditions are approached.

  5. Nanoscale Test Strips for Multiplexed Blood Analysis

    Science.gov (United States)

    Chan, Eugene

    2015-01-01

    A critical component of the DNA Medicine Institute's Reusable Handheld Electrolyte and Lab Technology for Humans (rHEALTH) sensor are nanoscale test strips, or nanostrips, that enable multiplexed blood analysis. Nanostrips are conceptually similar to the standard urinalysis test strip, but the strips are shrunk down a billionfold to the microscale. Each nanostrip can have several sensor pads that fluoresce in response to different targets in a sample. The strips carry identification tags that permit differentiation of a specific panel from hundreds of other nanostrip panels during a single measurement session. In Phase I of the project, the company fabricated, tested, and demonstrated functional parathyroid hormone and vitamin D nanostrips for bone metabolism, and thrombin aptamer and immunoglobulin G antibody nanostrips. In Phase II, numerous nanostrips were developed to address key space flight-based medical needs: assessment of bone metabolism, immune response, cardiac status, liver metabolism, and lipid profiles. This unique approach holds genuine promise for space-based portable biodiagnostics and for point-of-care (POC) health monitoring and diagnostics here on Earth.

  6. Comic Strips to Accompany Science Museum Exhibits

    Science.gov (United States)

    Chung, Beom Sun; Park, Eun-mi; Kim, Sang-Hee; Cho, Sook-kyoung; Chung, Min Suk

    2016-01-01

    Science museums make the effort to create exhibits with amusing explanations. However, existing explanation signs with lengthy text are not appealing, and as such, visitors do not pay attention to them. In contrast, conspicuous comic strips composed of simple drawings and humors can attract science museum visitors. This study attempted to reveal…

  7. Improved Lower Bound for Online Strip Packing

    NARCIS (Netherlands)

    Harren, Rolf; Kern, Walter

    We study the online strip packing problem and derive an improved lower bound of Ͽ ≥ 2.589... for the competitive ratio of this problem. The construction is based on modified “Brown-Baker-Katseff sequences‿ (Brown et al. in Acta Inform. 18:207–225, 1982) using only two types of rectangles. In

  8. Polymer Inclusion Membranes with Strip Dispersion

    Directory of Open Access Journals (Sweden)

    Yueh-Hsien Li

    2017-06-01

    Full Text Available The present work investigated the permeation of indium ions through a polymer inclusion membrane (PIM, prepared with cellulose triacetate (CTA as the base polymer, tris(2-butoxyethyl phosphate (TBEP as the plasticizer and di-(2-ethylhexylphosphoric acid (D2EHPA as the extractant. With 5 M HCl aqueous solution as the strip solution, we observed an initial indium permeability of 2.4 × 10−4 m/min. However, the permeability decreases with time, dropping to about 3.4 × 10−5 m/min after 200 min of operation. Evidence was obtained showing that hydrolysis of CTA occurred, causing a dramatic decrease in the feed pH (protons transported from strip to feed solutions and a loss of extractant and plasticizer from the membrane, and then leading to the loss of indium permeability. To alleviate the problem of hydrolysis, we proposed an operation scheme called polymer inclusion membranes with strip dispersion: dispersing the strip solution in extractant-containing oil and then bringing the dispersion to contact with the polymer membrane. Since the strong acid was dispersed in oil, the membrane did not directly contact the strong acid at all times, and membrane hydrolysis was thus alleviated and the loss of indium permeability was effectively prevented. With the proposed scheme, a stable indium permeability of 2.5 × 10−4 m/min was obtained during the whole time period of the permeation experiment.

  9. Inadvertent femoral artery "stripping": surgical management.

    Science.gov (United States)

    Liddicoat, J E; Bekassy, S M; Daniell, M B; De Bakey, M E

    1975-02-01

    Following "vein stripping" for varicosities, two patients were referred to our service for evaluation of arterial insufficiency of the lower extremities. Both patients had had surgical interruption of the femoral arterial system which required reconstruction. This paper emphasizes the importance of understanding surgical anatomy and presents the techniques of successful surgical management of both cases.

  10. ME1/1 Cathode Strip Chambers

    CERN Document Server

    Erchov, Yu V; Kamenev, Alexey; Karjavin, Vladimir; Khabarov, Serguei; Moissenz, P V; Moissenz, K P; Movchan, Sergey; Perelygin, Victor; Vassiliev, S E; Zarubin, Anatoli; Tchekhovski, V A

    2008-01-01

    The 76 innermost ME1/1 cathode strip chambers (CSC) of the CMS Experiment were designed and produced in Dubna. The chambers have been installed in the detector and commissioning has been completed. This paper describes the design of the CSCs, their main mechanical parameters and read-out electronics, and the results of tests with cosmic-ray muons.

  11. Cardiac Muscle Studies with Rat Ventricular Strips

    Science.gov (United States)

    Whitten, Bert K.; Faleschini, Richard J.

    1977-01-01

    Details undergraduate physiology laboratory experiments that demonstrate mechanical properties of cardiac muscle, using strips from the ventricle of a rat heart. Includes procedures for obtaining length-tension curves, demonstrating the role of calcium in excitation-contraction coupling, and showing effects of several cardiovascular drugs…

  12. Anodic Stripping Voltammetry: An Instrumental Analysis Experiment.

    Science.gov (United States)

    Wang, Joseph

    1983-01-01

    Describes an experiment designed to acquaint students with the theory and applications of anodic stripping voltammetry (ASV) as well as such ASV problems as contamination associated with trace analysis. The experimental procedure, instrumentation, and materials discussed are designed to minimize cost and keep procedures as simple as possible. (JM)

  13. Hardness of approximation for strip packing

    DEFF Research Database (Denmark)

    Adamaszek, Anna Maria; Kociumaka, Tomasz; Pilipczuk, Marcin

    2017-01-01

    [SODA 2016] have recently proposed a (1.4 + ϵ)-approximation algorithm for this variant, thus showing that strip packing with polynomially bounded data can be approximated better than when exponentially large values are allowed in the input. Their result has subsequently been improved to a (4/3 + ϵ...

  14. Refuges, flower strips, biodiversity and agronomic interest.

    Science.gov (United States)

    Roy, Grégory; Wateau, Karine; Legrand, Mickaël; Oste, Sandrine

    2008-01-01

    Several arthropods are natural predators of pests, and they are able to reduce and control their population development. FREDON Nord Pas-de-Calais (Federation Regionate de Defense contre les Organismes Nuisibles = Regional Federation for Pest Control) has begun for a long time to form farmers to the recognition of beneficial arthropods and to show them their usefulness. These beneficial insects or arachnids are present everywhere, in orchards and even in fields which are areas relatively poor in biodiversity. Adults feed in the flower strips instead larvae and some adults feed on preys such as aphids or caterpillars. Most of the time, beneficial insects can regulate pest but sometimes, in agricultural area, they can't make it early enough and efficiently. Their action begin too late and there biodiversity and number are too low. It's possible to enhance their action by manipulating the ecological infrastructures, like sewing flower strips or installing refuges. Flower strips increase the density of natural enemies and make them be present earlier in the field in order to control pests. Refuges permit beneficial's to spend winter on the spot. So they're able to be active and to grow in number earlier. From 2004 to 2007, on the one hand, FREDON Nord Pas-de-Calais has developed a research program. Its purpose was to inventory practices and also tools and means available and to judge the advisability of using such or such beneficial refuge in orchards. On the second hand, it studied the impact in orchard of refuges on population of beneficial's and the difference there were between manufactured refuges and homemade refuges. Interesting prospects were obtained with some of them. Otherwise, since 2003, FREDON has studied flower strips influence on beneficial population and their impact on pest control. In cabbage fields, results of trials have shown that flower strips lead to a reduction of aphid number under acceptable economic level, up to 50 meters from flower strips

  15. Dual Strip-Excited Dielectric Resonator Antenna with Parasitic Strips for Radiation Pattern Reconfigurability

    Directory of Open Access Journals (Sweden)

    M. Kamran Saleem

    2014-01-01

    Full Text Available A novel pattern reconfigurable antenna concept utilizing rectangular dielectric resonator antenna (DRA placed over dielectric substrate backed by a ground plane is presented. A dual strip excitation scheme is utilized and both excitation strips are connected together by means of a 50 Ω microstrip feed network placed over the substrate. The four vertical metallic parasitic strips are placed at corner of DRA each having a corresponding ground pad to provide a short/open circuit between the parasitic strip and antenna ground plane, through which a shift of 90° in antenna radiation pattern in elevation plane is achieved. A fractional bandwidth of approximately 40% at center frequency of 1.6 GHz is achieved. The DRA peak realized gain in whole frequency band of operation is found to be above 4 dB. The antenna configuration along with simulation and measured results are presented.

  16. Strip reduction testing of lubricants developed during ENFORM project

    DEFF Research Database (Denmark)

    Gazvoda, S.; Andreasen, Jan Lasson; Olsson, David Dam

    Strip reduction testing of lubricants developed during ENFORM project. Experiments were conducted with the strip reduction test [1] in order to classify experimental lubricants, developed during concerned project. One reference lubricant was used during testing.......Strip reduction testing of lubricants developed during ENFORM project. Experiments were conducted with the strip reduction test [1] in order to classify experimental lubricants, developed during concerned project. One reference lubricant was used during testing....

  17. Electrochemical Studies of Adsorption of Paraquat onto Ca10(PO46(OH2 from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Moulay Abderrahim EL MHAMMEDI

    2008-06-01

    Full Text Available Paraquat is one of the most widely used herbicides in the world. It has had a tarnished reputation because of its acute oral toxicity and ill-health associated with operators - particularly in the plantation sectors of many developing countries. Paraquat binds rapidly and tightly to clay materials in soils, and when adsorbed it is biologically inactive. It also binds to humus and other organic material: this results in no, or very low soil residues or leaching into water sources. This article presents a studies of kinetic of adsorption onto hydroxyapatite phosphocalcique Ca10(PO46(OH2 (HAP from aqueous solution. Measurements are performed by electrochemical methods using the cyclic voltammetric, chronoamperometry and square wave voltammetry at carbon paste electrode (CPE.

  18. Study on the sensitive and selective adsorption voltammetry of vanadium with antipyrylazo III (APA III)

    Energy Technology Data Exchange (ETDEWEB)

    Zhou Jinkui (Mainz Univ. (Germany). Inst. fuer Anorganische Chemie und Analytische Chemie); Neeb, R. (Mainz Univ. (Germany). Inst. fuer Anorganische Chemie und Analytische Chemie)

    1994-07-01

    The sensitive and selective adsorption voltammetric determination of the vanadium(V)-antipyrylazoIII complex in HAc-NaAc solution is investigated. The V-complex is strongly adsorbed onto a stationary Hg-electrode and is reduced at a potential more negative than that corresponding to the reduction of its ligand. The conditions for determining vanadium are investigated and the mechanism of the reduction peak of the vanadium complex is discussed, as also the influence of foreign ions on the determination of vanadium. And at least 20-fold excess of foreign ions does not cause any interference. The detection limit is 4 x 10[sup -10] mol/l V with 3 min enrichment time. (orig.)

  19. TOMOGRAPHIC MEASUREMENT OF LONGITUDINAL EMITTANCE GROWTH DUE TO STRIPPING FOILS.

    Energy Technology Data Exchange (ETDEWEB)

    MONTAG, C.; AHRENS, L.; THIEBERGER, P.

    2005-05-16

    During beam acceleration in the Brookhaven accelerator complex, heavy ions are stripped of their electrons in several steps. Depending on the properties of the stripping foils, this process results in an increased energy spread and longitudinal emittance growth. A tomographic phase space reconstruction technique has been applied to measure the associated emittance growth for different stripping foil materials.

  20. New insights into the chemistry of Coenzyme Q-0: A voltammetric and spectroscopic study.

    Science.gov (United States)

    Gulaboski, Rubin; Bogeski, Ivan; Kokoskarova, Pavlinka; Haeri, Haleh H; Mitrev, Sasa; Stefova, Marina; Stanoeva, Jasmina Petreska; Markovski, Velo; Mirčeski, Valentin; Hoth, Markus; Kappl, Reinhard

    2016-10-01

    Coenzyme Q-0 (CoQ-0) is the only Coenzyme Q lacking an isoprenoid group on the quinoid ring, a feature important for its physico-chemical properties. Here, the redox behavior of CoQ-0 in buffered and non-buffered aqueous media was examined. In buffered aqueous media CoQ-0 redox chemistry can be described by a 2-electron-2-proton redox scheme, characteristic for all benzoquinones. In non-buffered media the number of electrons involved in the electrode reaction of CoQ-0 is still 2; however, the number of protons involved varies between 0 and 2. This results in two additional voltammetric signals, attributed to 2-electrons-1H(+) and 2-electrons-0H(+) redox processes, in which mono- and di-anionic compounds of CoQ-0 are formed. In addition, CoQ-0 exhibits a complex chemistry in strong alkaline environment. The reaction of CoQ-0 and OH(-) anions generates several hydroxyl derivatives as products. Their structures were identified with HPLC/MS. The prevailing radical reaction mechanism was analyzed by electron paramagnetic resonance spectroscopy. The hydroxyl derivatives of CoQ-0 have a strong antioxidative potential and form stable complexes with Ca(2+) ions. In summary, our results allow mechanistic insights into the redox properties of CoQ-0 and its hydroxylated derivatives and provide hints on possible applications. Copyright © 2016 Elsevier B.V. All rights reserved.

  1. Enzyme-catalyzed reaction of voltammetric enzyme-linked immunoassay system based on OAP as substrate

    Institute of Scientific and Technical Information of China (English)

    张书圣; 陈洪渊; 焦奎

    1999-01-01

    The o-aminophenol (OAP)-H2O2-horseradish peroxidase (HRP) voltammetric enzyme-linked immunoassay new system has extremely high sensitivity. HRP can be measured with a detection limit of 6.0×10-(10) g/L and a linear range of 1.0×10-9—4.0×10-6 g/L. The pure product of H2O2 oxidizing OAP catalyzed by HRP was prepared with chemical method. The enzyme-catalyzed reaction has been investigated with electroanalytical chemistry, UV/Vis spectrum, IR spectrum, 13C NMR, 1H NMR, mass spectrum, elemental analysis, etc. Under the selected enzyme-catalyzed reaction conditions, the oxidation product of OAP with H2O2 catalyzed by HRP is 2-aminophe-noxazine-3-one. The processes of the enzyme-catalyzed reaction and the electroreduction of the product of the enzymecatalyzed reaction have been described.

  2. Voltammetric Determination of Paraquat Using Graphite Pencil Electrode Modified with Doped Polypyrrole

    CERN Document Server

    Sayyahmanesh, Maryam; Meibodi, Azam S Emami; Ahooyi, Taha Mohseni

    2016-01-01

    Recognition and determination of paraquat (PQ) using graphite pencil electrode (GPE) modified with polypyrrole (Ppy) doped with Eriochrome blue-black B (EBB) is reported. To that end, a thin film of Ppy was deposited onto the electrode surface by electropolymerization in the presence of a functional doping ion, EBB. The Ppy/EBB-coated electrode was templated by PQ ion and then the performance of the molecularly imprinted EBB/Ppy/GPE was evaluated by voltammetric technique. The prepared electrode exhibited considerable increase in electroactivity of the sensor toward this herbicide compared to the non-imprinted electrode. To enhance the detection capability of the prepared system, the factors controlling its response were investigated and optimized using differential pulse voltammetry. The proposed analytical procedure was proved to be applicable in the concentration range of 5 to 50 {\\mu}M (R^2 = 0.9939) and detection limit of (3{\\sigma}) 0.22 {\\mu}M. Ultimately, the proposed analytical methodology was applie...

  3. Voltammetric determination of antioxidant character in Berberis lycium Royel, Zanthoxylum armatum and Morus nigra Linn plants.

    Science.gov (United States)

    Ahmed, Safeer; Shakeel, Faria

    2012-07-01

    The antioxidant activity potential of three different plant extracts was investigated against superoxide anion radical while employing cyclic voltammetry technique. The plants Berberis lyceum Royle, Morus nigra Linn and Zanthoxylum armatum were selected because of their potential use in the traditional medicine. The voltammetric response of the electrochemically generated superoxide anion radial in DMSO was monitored in the absence and presence of the plat extracts. The decrease in the current was interpreted in terms of antiradical activity of the added extract. The thermodynamic feasibility of the radical scavenging by extracts was accounted in terms of antioxidant activity coefficient (K(ao)) and standard Gibbs free energy (ΔG(o)). The values of K(ao) and ΔG(o) ranged from 1.0 x 102 to 57 x 102 L(-1) and -18 to -27 kJmol(-1), respectively. The possible mechanism of the antioxidant reaction was regarded as E(r)C(i) mechanism i.e. reversible electron transfer followed by hydrogen atom transfer- an irreversible chemical reaction.

  4. Classification and prediction of rice wines with different marked ages by using a voltammetric electronic tongue.

    Science.gov (United States)

    Wei, Zhenbo; Wang, Jun; Ye, Linshuang

    2011-08-15

    A voltammetric electronic tongue (VE-tongue) was developed to discriminate the difference between Chinese rice wines in this research. Three types of Chinese rice wine with different marked ages (1, 3, and 5 years) were classified by the VE-tongue by principal component analysis (PCA) and cluster analysis (CA). The VE-tongue consisted of six working electrodes (gold, silver, platinum, palladium, tungsten, and titanium) in a standard three-electrode configuration. The multi-frequency large amplitude pulse voltammetry (MLAPV), which consisted of four segments of 1 Hz, 10 Hz, 100 Hz, and 1000 Hz, was applied as the potential waveform. The three types of Chinese rice wine could be classified accurately by PCA and CA, and some interesting regularity is shown in the score plots with the help of PCA. Two regression models, partial least squares (PLS) and back-error propagation-artificial neural network (BP-ANN), were used for wine age prediction. The regression results showed that the marked ages of the three types of Chinese rice wine were successfully predicted using PLS and BP-ANN.

  5. Detection of antibiotic residues in bovine milk by a voltammetric electronic tongue system.

    Science.gov (United States)

    Wei, Zhenbo; Wang, Jun

    2011-05-23

    A voltammetric electronic tongue (VE-tongue) was developed to detect antibiotic residues in bovine milk. Six antibiotics (Chloramphenicol, Erythromycin, Kanamycin sulfate, Neomycin sulfate, Streptomycin sulfate and Tetracycline HCl) spiked at four different concentration levels (0.5, 1, 1.5 and 2 maximum residue limits (MRLs)) were classified based on VE-tongue by two pattern recognition methods: principal component analysis (PCA) and discriminant function analysis (DFA). The VE-tongue was composed of five working electrodes (gold, silver, platinum, palladium, and titanium) positioned in a standard three-electrode configuration. The Multi-frequency large amplitude pulse voltammetry (MLAPV) which consisted of four segments (1 Hz, 10 Hz, 100 Hz and 1000 Hz) was applied as potential waveform. The six antibiotics at the MRLs could not be separated from bovine milk completely by PCA, but all the samples were demarcated clearly by DFA. Three regression models: Principal Component Regression Analysis (PCR), Partial Least Squares Regression (PLSR), and Least Squares-Support Vector Machines (LS-SVM) were used for concentrations of antibiotics prediction. All the regression models performed well, and PCR had the most stable results.

  6. Detection of antibiotic residues in bovine milk by a voltammetric electronic tongue system

    Energy Technology Data Exchange (ETDEWEB)

    Wei Zhenbo [Zhejiang University, Department of Bio-Systems Engineering, 268 Kaixuan Road, Hangzhou, Zhejiang 310029 (China); Wang Jun, E-mail: jwang@zju.edu.cn [Zhejiang University, Department of Bio-Systems Engineering, 268 Kaixuan Road, Hangzhou, Zhejiang 310029 (China)

    2011-05-23

    A voltammetric electronic tongue (VE-tongue) was developed to detect antibiotic residues in bovine milk. Six antibiotics (Chloramphenicol, Erythromycin, Kanamycin sulfate, Neomycin sulfate, Streptomycin sulfate and Tetracycline HCl) spiked at four different concentration levels (0.5, 1, 1.5 and 2 maximum residue limits (MRLs)) were classified based on VE-tongue by two pattern recognition methods: principal component analysis (PCA) and discriminant function analysis (DFA). The VE-tongue was composed of five working electrodes (gold, silver, platinum, palladium, and titanium) positioned in a standard three-electrode configuration. The Multi-frequency large amplitude pulse voltammetry (MLAPV) which consisted of four segments (1 Hz, 10 Hz, 100 Hz and 1000 Hz) was applied as potential waveform. The six antibiotics at the MRLs could not be separated from bovine milk completely by PCA, but all the samples were demarcated clearly by DFA. Three regression models: Principal Component Regression Analysis (PCR), Partial Least Squares Regression (PLSR), and Least Squares-Support Vector Machines (LS-SVM) were used for concentrations of antibiotics prediction. All the regression models performed well, and PCR had the most stable results.

  7. Voltammetric and mathematical evidence for dual transport mediation of serotonin clearance in vivo.

    Science.gov (United States)

    Wood, Kevin M; Zeqja, Anisa; Nijhout, H Frederik; Reed, Michael C; Best, Janet; Hashemi, Parastoo

    2014-08-01

    The neurotransmitter serotonin underlies many of the brain's functions. Understanding serotonin neurochemistry is important for improving treatments for neuropsychiatric disorders such as depression. Antidepressants commonly target serotonin clearance via serotonin transporters and have variable clinical effects. Adjunctive therapies, targeting other systems including serotonin autoreceptors, also vary clinically and carry adverse consequences. Fast scan cyclic voltammetry is particularly well suited for studying antidepressant effects on serotonin clearance and autoreceptors by providing real-time chemical information on serotonin kinetics in vivo. However, the complex nature of in vivo serotonin responses makes it difficult to interpret experimental data with established kinetic models. Here, we electrically stimulated the mouse medial forebrain bundle to provoke and detect terminal serotonin in the substantia nigra reticulata. In response to medial forebrain bundle stimulation we found three dynamically distinct serotonin signals. To interpret these signals we developed a computational model that supports two independent serotonin reuptake mechanisms (high affinity, low efficiency reuptake mechanism, and low affinity, high efficiency reuptake system) and bolsters an important inhibitory role for the serotonin autoreceptors. Our data and analysis, afforded by the powerful combination of voltammetric and theoretical methods, gives new understanding of the chemical heterogeneity of serotonin dynamics in the brain. This diverse serotonergic matrix likely contributes to clinical variability of antidepressants. © 2014 International Society for Neurochemistry.

  8. Mesoporous carbon-containing voltammetric biosensor for determination of tyramine in food products.

    Science.gov (United States)

    Kochana, Jolanta; Wapiennik, Karolina; Knihnicki, Paweł; Pollap, Aleksandra; Janus, Paula; Oszajca, Marcin; Kuśtrowski, Piotr

    2016-07-01

    A voltammetric biosensor based on tyrosinase (TYR) was developed for determination of tyramine. Carbon material (multi-walled carbon nanotubes or mesoporous carbon CMK-3-type), polycationic polymer-i.e., poly(diallyldimethylammonium chloride) (PDDA), and Nafion were incorporated into titania dioxide sol (TiO2) to create an immobilization matrix. The features of the formed matrix were studied by scanning electron microscopy (SEM) and cyclic voltammetry (CV). The analytical performance of the developed biosensor was evaluated with respect to linear range, sensitivity, limit of detection, long-term stability, repeatability, and reproducibility. The biosensor exhibited electrocatalytic activity toward tyramine oxidation within a linear range from 6 to 130 μM, high sensitivity of 486 μA mM(-1) cm(-2), and limit of detection of 1.5 μM. The apparent Michaelis-Menten constant was calculated to be 66.0 μM indicating a high biological affinity of the developed biosensor for tyramine. Furthermore, its usefulness in determination of tyramine in food product samples was also verified. Graphical abstract Different food samples were analyzed to determine tyramine using biosensor based on tyrosinase.

  9. On the Nature of Voltammetric Signals Originating from Hydrogen Electrosorption into Palladium-Noble Metal Alloys

    Science.gov (United States)

    Łukaszewski, Mariusz; Hubkowska, Katarzyna; Koss, Urszula; Czerwiński, Andrzej

    2013-01-01

    Hydrogen sorption/desorption signals observed on cyclic voltammograms in experiments on hydrogen electrosorption into Pd-noble metal alloys (Pd-Au, Pd-Pt, Pd-Rh, Pd-Ru, Pd-Pt-Rh, Pd-Pt-Au) were characterized. The influence of electrosorption potential, scan rate and alloy bulk composition on the features of the hydrogen peaks was investigated. The experimental results were compared with those obtained on the basis of a model taken from the literature. It was confirmed that the rate of the α-β phase transition controls the overall rate of the process of hydrogen absorption/desorption into/from thin Pd-based electrodes. It was demonstrated that from the analysis of the changes of the hydrogen oxidation peak potential with the hydrogen electrosorption potential in cyclic voltammetric experiments it is possible to determine the limiting Pd bulk content, below which the β-phase in the alloy-hydrogen system is not formed. PMID:28788362

  10. Simultaneous Voltammetric/Amperometric Determination of Sulfide and Nitrite in Water at BDD Electrode

    Directory of Open Access Journals (Sweden)

    Anamaria Baciu

    2015-06-01

    Full Text Available This work reported new voltammetric/amperometric-based protocols using a commercial boron-doped diamond (BDD electrode for simple and fast simultaneous detection of sulfide and nitrite from water. Square-wave voltammetry operated under the optimized working conditions of 0.01 V step potential, 0.5 V modulation amplitude and 10 Hz frequency allowed achieving the best electroanalytical parameters for the simultaneous detection of nitrite and sulfide. For practical in-field detection applications, the multiple-pulsed amperometry technique was operated under optimized conditions, i.e., −0.5 V/SCE for a duration of 0.3 s as conditioning step, +0.85 V/SCE for a duration of 3 s that assure the sulfide oxidation and +1.25 V/SCE for a duration of 0.3 s, where the nitrite oxidation occurred, which allowed the simultaneously detection of sulfide and nitrite without interference between them. Good accuracy was found for this protocol in comparison with standardized methods for each anion. Also, no interference effect was found for the cation and anion species, which are common in the water matrix.

  11. Simultaneous Voltammetric/Amperometric Determination of Sulfide and Nitrite in Water at BDD Electrode

    Science.gov (United States)

    Baciu, Anamaria; Ardelean, Magdalena; Pop, Aniela; Pode, Rodica; Manea, Florica

    2015-01-01

    This work reported new voltammetric/amperometric-based protocols using a commercial boron-doped diamond (BDD) electrode for simple and fast simultaneous detection of sulfide and nitrite from water. Square-wave voltammetry operated under the optimized working conditions of 0.01 V step potential, 0.5 V modulation amplitude and 10 Hz frequency allowed achieving the best electroanalytical parameters for the simultaneous detection of nitrite and sulfide. For practical in-field detection applications, the multiple-pulsed amperometry technique was operated under optimized conditions, i.e., −0.5 V/SCE for a duration of 0.3 s as conditioning step, +0.85 V/SCE for a duration of 3 s that assure the sulfide oxidation and +1.25 V/SCE for a duration of 0.3 s, where the nitrite oxidation occurred, which allowed the simultaneously detection of sulfide and nitrite without interference between them. Good accuracy was found for this protocol in comparison with standardized methods for each anion. Also, no interference effect was found for the cation and anion species, which are common in the water matrix. PMID:26102487

  12. Gold nanoparticles modified carbon paste electrode for differential pulse voltammetric determination of eugenol.

    Science.gov (United States)

    Afzali, Daryoush; Zarei, Somaye; Fathirad, Fariba; Mostafavi, Ali

    2014-10-01

    In the present study, a carbon paste electrode chemically modified with gold nanoparticles was used as a sensitive electrochemical sensor for determination of eugenol. The differential pulse voltammetric method was employed to study the behavior of eugenol on this modified electrode. The effect of variables such as percent of gold nanoparticles, pH of solution, accumulation potential and time on voltammogram peak current were optimized. The proposed electrode showed good oxidation response for eugenol in 0.1 mol L(-1) phosphate buffer solution (pH8) and the peak potential was about +285 mV (vs. Ag/AgCl). The peak current increased linearly with the eugenol concentration in the range of 5-250 μmol L(-1). The detection limit was found to be 2.0 μmol L(-1) and the relative standard deviation was 1.2% (n=7). The effect of interferences on the eugenol peak current was studied. The method has been applied to the determination of eugenol in different real samples, spiked recoveries were in the range of 96%-99%.

  13. Differential pulse voltammetric determination of eugenol at a pencil graphite electrode.

    Science.gov (United States)

    Sağlam, Özlem; Dilgin, Didem Giray; Ertek, Bensu; Dilgin, Yusuf

    2016-03-01

    In this study, the electrochemical behavior of eugenol, a widely used herbal drug, was investigated at a pencil graphite electrode (PGE). A low-cost, disposable, sensitive and selective electrochemical sensor is proposed for the determination of eugenol by recording its differential pulse voltammograms in Britton-Robinson buffer solution containing 0.1 M KCl with pH of 2.0 at the PGE. The PGE displayed a very good electrochemical behavior with significant enhancement of the peak current compared to a glassy carbon electrode. Under experimental conditions, the PGE had a linear response range from 0.3 μM to 50.0 μM eugenol with a detection limit of 0.085 μM (based on 3S(b)). Relative standard deviations of 2.4 and 4.8% were obtained for five successive determinations of 30.0 and 5.0 μM eugenol, respectively, which indicate acceptable repeatability. This voltammetric method was successfully applied for the direct determination of eugenol in real samples. The effect of various interfering compounds on the eugenol peak current was also studied.

  14. Maize tassel-modified carbon paste electrode for voltammetric determination of Cu(II).

    Science.gov (United States)

    Moyo, Mambo; Okonkwo, Jonathan O; Agyei, Nana M

    2014-08-01

    The preparation and application of a practical electrochemical sensor for environmental monitoring and assessment of heavy metal ions in samples is a subject of considerable interest. In this paper, a carbon paste electrode modified with maize tassel for the determination of Cu(II) has been proposed. Scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) were used to study morphology and identify the functional groups on the modified electrode, respectively. First, Cu(II) was adsorbed on the carbon paste electrode surface at open circuit and voltammetric techniques were used to investigate the electrochemical performances of the sensor. The electrochemical sensor showed an excellent electrocatalytic activity towards Cu(II) at pH 5.0 and by increasing the amount of maize tassel biomass, a maximum response at 1:2.5 (maize tassel:carbon paste; w/w) was obtained. The electrocatalytic redox current of Cu(II) showed a linear response in the range (1.23 μM to 0.4 mM) with the correlation coefficient of 0.9980. The limit of detection and current-concentration sensitivity were calculated to be 0.13 (±0.01) μM and 0.012 (±0.001) μA/μM, respectively. The sensor gave good recovery of Cu(II) in the range from 96.0 to 98.0 % when applied to water samples.

  15. Relative reactivity of dihydropyridine derivatives to electrogenerated superoxide ion in DMSO solutions: a voltammetric approach.

    Science.gov (United States)

    Oriz, María Eugenia; Núñez-Vergara, Luis Joaquin; Squella, Juan Arturo

    2003-02-01

    To evaluate the reaction of a large series of pharmacologically significant 1,4-dihydropyridine (1,4-DHP) compounds with superoxide (O2.-) in dimethylsulfoxide using differential pulse voltammetry and controlled potential electrolysis. Differential pulse voltammetry was used to track the consumption of O2.-, and controlled potential electrolysis was used to electrogenerate O2.-. With the addition of 1,4-DHP, the oxidation peak current of O2.- decreased concentration dependently, suggesting that 1,4-DHP reacts with O2.-, that is, 1,4-DHP scavenges O2.- in dimethylsulfoxide. very easy and direct voltammetric procedure to study the relative reactivity of different 1,4-DHP with O2.- is proposed. Using the proposed method we have found that all commercial 1,4-DHP reacts with O2.-. The following order of rates was obtained: felodipine > or = vitamin E > isradipine > nimodipine > furnidipine > nitrendipine > nisoldipine > nifedipine. Furthermore, it was demonstrated that the hydrogen at the N-position of 1,4-DHP compounds could be released as a proton in the presence of O2.-, thus the electrogenerated O2.- worked as a proton acceptor to 1,4-DHP.

  16. Voltammetric Electronic Tongue for Discrimination of Milk Adulterated with Urea, Formaldehyde and Melamine

    Directory of Open Access Journals (Sweden)

    Lígia Bueno

    2014-11-01

    Full Text Available We report the fabrication of a voltammetric electronic tongue for the detection and discrimination of harmful substances intentionally added to milk to increase its shelf life or imitate protein content. The electronic tongue consisted of three working electrodes composed of platinum, gold, and copper. The measurement principles involved the extraction of information from cyclic voltammograms recorded in unadulterated and adulterated milk. The extracted data were analysed using principal component analysis and the contaminants were successfully differentiated from one another in a score plot. Electrochemical quartz crystal microbalance analysis was used to investigate the electrode response in order to understand the mechanism by which the tongue could discriminate between the samples. It was found that the electrochemical formation and dissolution of platinum and gold oxides, and the reduction of a copper-melamine ionic pair formed at the surface of the copper electrode were the main factors responsible for discrimination. In addition, the electronic tongue was capable of identifying adulterations in different types of milk (whole, skimmed, and semi-skimmed and milk from different brands. The lowest concentration of adulterant that resulted in a good discrimination was 10.0, 4.16, and 0.95 mmol·L−1 for formaldehyde, urea, and melamine, respectively.

  17. Simultaneous Voltammetric/Amperometric Determination of Sulfide and Nitrite in Water at BDD Electrode.

    Science.gov (United States)

    Baciu, Anamaria; Ardelean, Magdalena; Pop, Aniela; Pode, Rodica; Manea, Florica

    2015-06-19

    This work reported new voltammetric/amperometric-based protocols using a commercial boron-doped diamond (BDD) electrode for simple and fast simultaneous detection of sulfide and nitrite from water. Square-wave voltammetry operated under the optimized working conditions of 0.01 V step potential, 0.5 V modulation amplitude and 10 Hz frequency allowed achieving the best electroanalytical parameters for the simultaneous detection of nitrite and sulfide. For practical in-field detection applications, the multiple-pulsed amperometry technique was operated under optimized conditions, i.e., -0.5 V/SCE for a duration of 0.3 s as conditioning step, +0.85 V/SCE for a duration of 3 s that assure the sulfide oxidation and +1.25 V/SCE for a duration of 0.3 s, where the nitrite oxidation occurred, which allowed the simultaneously detection of sulfide and nitrite without interference between them. Good accuracy was found for this protocol in comparison with standardized methods for each anion. Also, no interference effect was found for the cation and anion species, which are common in the water matrix.

  18. Synthesis, characterization and cyclic voltammetric study of copper(II) and nickel(II) polymer chelates.

    Science.gov (United States)

    Azmeera, Venkanna; Rastogi, Pankaj Kumar; Adhikary, Pubali; Ganesan, Vellaichamy; Krishnamoorthi, S

    2014-09-22

    Graft copolymers based on dextran (Dx) and 2-acrylamido-2-methyl-1-propane sulphonic acid (AMPS) were synthesized by free radical initiated solution polymerization technique using ceric ammonium nitrate as initiator. These graft copolymers were used to prepare Cu(II) and Ni(II) chelates by reactions with Cu(II) and Ni(II) metal ions respectively. Graft copolymer and metal chelates were characterized by elemental analysis, intrinsic viscosity, FT-IR, scanning electron microscopy (SEM), atomic force microscopy (AFM), thermogravimetric analysis (TGA) and powder X-ray diffraction (XRD). Elemental analysis, intrinsic viscosity and FT-IR studies revealed the incorporation of metal ions to form metal chelates. SEM studies showed the change in morphology due to metal incorporation. From AFM studies it was observed that there was increase in Root mean square (RMS) roughness values in case of metal complexes. Metal chelates were observed to be thermally more stable than graft copolymer from TGA. UV-vis spectroscopy study revealed increase in absorbance values and cyclic voltammetric (CV) studies showed more than tenfold increase in redox current due to formation of Cu(II) and Ni(II) metal chelates. The binding constants of each complex determined by using UV-visible spectroscopy revealed that Cu(II) has more binding ability than Ni(II).

  19. Bird community response to filter strips in Maryland

    Science.gov (United States)

    Blank, P.J.; Dively, G.P.; Gill, D.E.; Rewa, C.A.

    2011-01-01

    Filter strips are strips of herbaceous vegetation planted along agricultural field margins adjacent to streams or wetlands and are designed to intercept sediment, nutrients, and agrichemicals. Roughly 16,000 ha of filter strips have been established in Maryland through the United States Department of Agriculture's Conservation Reserve Enhancement Program. Filter strips often represent the only uncultivated herbaceous areas on farmland in Maryland and therefore may be important habitat for early-successional bird species. Most filter strips in Maryland are planted to either native warm-season grasses or cool-season grasses and range in width from 10.7 m to 91.4 m. From 2004 to 2007 we studied the breeding and wintering bird communities in filter strips adjacent to wooded edges and non-buffered field edges and the effect that grass type and width of filter strips had on bird community composition. We used 5 bird community metrics (total bird density, species richness, scrub-shrub bird density, grassland bird density, and total avian conservation value), species-specific densities, nest densities, and nest survival estimates to assess the habitat value of filter strips for birds. Breeding and wintering bird community metrics were greater in filter strips than in non-buffered field edges but did not differ between cool-season and warm-season grass filter strips. Most breeding bird community metrics were negatively related to the percent cover of orchardgrass (Dactylis glomerata) in ???1 yr. Breeding bird density was greater in narrow (60 m) filter strips. Our results suggest that narrow filter strips adjacent to wooded edges can provide habitat for many bird species but that wide filter strips provide better habitat for grassland birds, particularly obligate grassland species. If bird conservation is an objective, avoid planting orchardgrass in filter strips and reduce or eliminate orchardgrass from filter strips through management practices. Copyright ?? 2011 The

  20. Improving Thin Strip Profile Using Work Roll Cross and Work Roll Shifting Methods in Cold Strip Rolling

    Directory of Open Access Journals (Sweden)

    Hasan Tibar

    2017-01-01

    Full Text Available The optimization of rolling parameters in order to achieve better strip shape and to reduce rolling force is a challenge in rolling practice. In this paper, thin strip asymmetrical rolling of aluminum at various speed ratios under lubricated condition has been investigated at various combinations of work rolls cross (WRC angles and work rolls shifting (WRS values. The effects of strip width, reduction, and rolling speed on strip shape taking WRC and WRS into consideration are discussed. Results show that strip profile improves significantly when the WRC angle is increased from 0° to 1°, with an associated reduction in rolling force. Increasing WRS value from 0 to 8 mm improves the strip profile as well but not as significantly as when WRC angle is increased. No significant improvement was found in strip shape when the strip width was increased. At higher reduction, the strip shape was improved; a decrease in the rolling force was also observed. A higher speed ratio was found to be effective only at a higher WRC angle. The effect of lubrication on the strip profile was significant. Results indicate that an optimum combination of WRC, WRS, reduction, width, and speed ratio under lubricated conditions can ensure an improved exit strip profile, reduce rolling force, and obtain a better quality strip.

  1. Shape Setup System for 1700 Hot Strip Mill

    Institute of Scientific and Technical Information of China (English)

    GUO Zhong-feng; XU Jian-zhong; LI Chang-sheng; LIU Xiang-hua

    2007-01-01

    Shape setup (SSU) system is the core technology for hot strip mill (HSM). A precise SSU system was used to improve the strip quality for HSM. The function of SSU, setup, and feedback was introduced. The main mathematical models of roll gap profile and longitudinal strain difference are set up. Strip profile allocation strategy was researched according to the SSU system of a domestic 1 700 mm HSM. The SSU system was put into practical use and the measurement results showed that strip flatness variation and strip profile variation could be controlled in target scope.

  2. The Formation and Evolution of Stripped Dark Matter Halos

    Science.gov (United States)

    Zhu, Jessica; Tuan, Austin Zong; Lee, Christoph; Primack, Joel R.

    2016-01-01

    We implement a model to describe the density profiles of stripped dark matter halos. Our model generalizes the Navarro-Frenk-White (NFW) distribution to allow for more flexibility in the slope of the outer halo. We find that the density distributions of stripped halos tend to have outer slopes steeper than assumed by the NFW distribution. We also examine the relationship between severity of stripping and halo shape, spin parameter and concentration, and find that highly stripped halos are more spheroidal, have lower spin parameters, and have higher concentrations compared to less stripped halos.

  3. Direct in situ measurement of dissolved zinc in the presence of zinc oxide nanoparticles using anodic stripping voltammetry.

    Science.gov (United States)

    Jiang, Chuanjia; Hsu-Kim, Heileen

    2014-11-01

    The wide use of metal-based nanomaterials such as zinc oxide (ZnO) nanoparticles (NPs) has generated concerns regarding their environmental and health risks. For ZnO NPs, their toxicity in aquatic systems often depends on the release of dissolved zinc species, and the rate of dissolution is influenced by water chemistry, including the presence of zinc-chelating ligands. A challenge, however, remains in quantifying the dissolution of ZnO NPs, particularly for time scales that are short enough to determine rates. This paper reports the application of anodic stripping voltammetry (ASV) with a hanging mercury drop electrode to directly measure the concentration of dissolved zinc in ZnO NP suspensions, without separation of the ZnO NPs from the aqueous phase. The effects of the deposition time and the electrochemical potential scan rate on the ASV measurement were consistent with expectations for dissolved phase measurements. The dissolved zinc concentration measured by ASV ([Zn]ASV) was compared with that measured by inductively coupled plasma mass spectrometry (ICP-MS) after ultracentrifugation ([Zn]ICP-MS), for four types of ZnO NPs with different coatings and primary particle diameters. For small ZnO NPs (4-5 nm), [Zn]ASV was 20% higher than [Zn]ICP-MS, suggesting that these small NPs contributed to the voltammetric measurement. For larger ZnO NPs (approximately 20 nm), [Zn]ASV was (79 ± 19)% of [Zn]ICP-MS, despite the high concentrations of ZnO NPs in suspension. Using ASV, the dissolution of ZnO NPs was studied, with or without Suwannee River Fulvic Acid (SRFA). Although SRFA diminished the ASV stripping current, dissolution of 20 nm ZnO NPs was significantly promoted at high fulvic acid to ZnO NP ratios. The ASV method described in this paper provides a useful tool for studying the dissolution kinetics of ZnO NPs in complex environmental matrices.

  4. Mechanics of Thin Strip Steering in Hot Rolling

    Science.gov (United States)

    Jiang, Zhengyi; Tieu, Kiet A.

    2004-06-01

    The hot rolling of thin strip can result in several problems in hot rolling, for instance, the control of strip steering, strip shape and flatness and surface roughness etc. Therefore, the hot rolling of thin strip brings out a requirement of innovative technologies such as the extended control of shape and flatness, steering control and reduction of load by roll gap lubrication. In this paper, the authors focus on the analysis of thin strip snaking movement, as well as solve the related problems such as the shape and flatness due to a larger reduction applied when the strip is thinner. A finite element method was used to simulate this nonsymmetricity rolling considering the non-uniform reduction along the strip width. The calculated spread is compared with the measured values obtained from the rolling mill in laboratory and the friction effect is also discussed.

  5. Antenna with distributed strip and integrated electronic components

    Science.gov (United States)

    Rodenbeck, Christopher T.; Payne, Jason A.; Ottesen, Cory W.

    2008-08-05

    An antenna comprises electrical conductors arranged to form a radiating element including a folded line configuration and a distributed strip configuration, where the radiating element can be in proximity to a ground conductor and/or arranged as a dipole. Embodiments of the antenna include conductor patterns formed on a printed wiring board, having a ground plane, spacedly adjacent to and coplanar with the radiating element. An antenna can comprise a distributed strip patterned on a printed wiring board, integrated with electronic components mounted on top of or below the distributed strip, and substantially within the extents of the distributed strip. Mounting of electronic components on top of or below the distributed strip has little effect on the performance of the antenna, and allows for realizing the combination of the antenna and integrated components in a compact form. An embodiment of the invention comprises an antenna including a distributed strip, integrated with a battery mounted on the distributed strip.

  6. PRESUPPOSITIONS AND IMPLICATURES IN COMIC STRIPS

    Directory of Open Access Journals (Sweden)

    Ienneke Indra Dewi

    2008-05-01

    Full Text Available Article aimed to find out the role of presuppositions, implicatures, as well as to see the maxims violated or flouted in the comic strips i.e. to whether there is a miscommunication among the characters in the comic strips. Data were taken from the three comics, those are Peanuts, Andy, and Tintin, and were analysed based on the pattern that the sender made a presupposition before transferring information and the receiver would try to get the implied message. The results show that presuppositions and implicatures are much influenced by the background knowledge. The more the speaker and hearer know each other’s background, the better presuppositions and implicatures they make and finally, the less miscommunication occurred.

  7. Operation of a Batch Stripping Distillation Column

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A stripping batch distillation column is preferred when the amount of the light component in the feed is small and the products are to be recovered at high purity. The operation modes of a batch stripping are believed to be the same as those of a rectifier. However, the control system of a stripper is different. In this paper, we explore three different control methods with Hysys (Hyprotech Ltd. 1997) for a batch stripper. The main difference is the control scheme for reboiler liquid level: (a) controlled by reflux flow; (b) controlled by reboiler heat duty; (c) controlled by bottom product flow. The main characteristics of operating a batch stripper with different control scheme are presented in this paper. Guidelines are provided for the startup of a batch stripper, the effects of somecontrol tuning parameters on the column performance are discussed.

  8. L-strip proximity fed ga

    Directory of Open Access Journals (Sweden)

    Ashish Singh

    2014-03-01

    Full Text Available In this article, the analysis of dualband L-strip fed compact semi-circular disk microstrip patch antenna has been presented using circuit theory concept. The antenna parameters such as return loss, VSWR and radiation pattern are calculated. The effect of geometric dimensions of the proposed antenna such as length of vertical and horizontal portion of L-strip is investigated. It is found that antenna resonate at two distinct modes i.e. 1.3 GHz and 6.13 GHz for lower and upper resonance frequencies respectively. The bandwidth of the proposed antenna at lower resonance frequency is 6.61% (simulated and 10.64% (theoretical whereas at upper resonance frequency, it is 6.02% (simulated and 9.06 % (theoretical. The theoretical results are compared with IE3D simulation results as well as experimental results and they are in close agreement.

  9. Frequency dependent magnetization of superconductor strip

    Energy Technology Data Exchange (ETDEWEB)

    Thakur, Kailash Prasad [Landcare Research, Palmerston North (New Zealand); Raj, Ashish [Computer Science in Radiology, Weill Medical College, Cornell University, NY (United States); Brandt, Ernst Helmut [Max-Planck-Institut fuer Metallforschung, POB 800665, D-70506 Stuttgart (Germany); Sastry, Pamidi V P S S, E-mail: thakurk@landcareresearch.co.nz, E-mail: asr2004@med.cornell.edu, E-mail: ehb@mf.mpg.de, E-mail: pamidi@caps.fsu.edu [Center for Advanced Power Systems, Florida State University, Tallahassee, FL 32310 (United States)

    2011-04-15

    The frequency dependence of magnetic ac loss of thin superconductor strip subjected to an ac magnetic field perpendicular to the surface of the strip is investigated by incorporating a flux creep model into the critical state model of Brandt and Indenbom. It is found that the reduced ac loss exhibits a maximum value at a frequency f{sub m}, which is a rapidly varying function of the applied ac magnetic field. At low magnetic field, f{sub m} becomes zero, and ac loss decreases with frequency as a power law ({approx}f{sup -2/n}). Whereas at high magnetic field f{sub m} becomes infinite and ac loss increases with frequency, still following the power law ({approx}f{sup 1/n}). The analytical results are substantiated with experimental data and the results of a 2D finite element simulation.

  10. The Extent of the Stop Coannihilation Strip

    CERN Document Server

    Ellis, John; Zheng, Jiaming

    2014-01-01

    Many supersymmetric models such as the CMSSM feature a strip in parameter space where the lightest neutralino \\chi is identified as the lightest supersymmetric particle (LSP), the lighter stop squark \\tilde t_1 is the next-to-lightest supersymmetric particle (NLSP), and the relic \\chi cold dark matter density is brought into the range allowed by astrophysics and cosmology by coannihilation with the lighter stop squark \\tilde t_1 NLSP. We calculate the stop coannihilation strip in the CMSSM, incorporating Sommerfeld enhancement effects, and explore the relevant phenomenological constraints and phenomenological signatures. In particular, we show that the \\tilde t_1 may weigh several TeV, and its lifetime may be in the nanosecond range, features that are more general than the specific CMSSM scenarios that we study in this paper.

  11. Coiling Temperature Control in Hot Strip Mill

    Science.gov (United States)

    Imanari, Hiroyuki; Fujiyama, Hiroaki

    Coiling temperature is one of the most significant factors in products of hot strip mill to determine material properties such as strength, toughness of steel, so it is very important to achieve accurate coiling temperature control (CTC). Usually there are a few pyrometers on the run out table in hot strip mill, therefore temperature model and its adapting system have large influences on the accuracy of CTC. Also unscheduled change of rolling speed has a bad effect to keep coiling temperature as its target. Newly developed CTC system is able to get very accurate coiling temperature against uncertain factors and disturbances by adopting easily identified temperature model, learning method and dynamic set up function. The features of the CTC system are discussed with actual data, and the effectiveness of the system is shown by actual control results.

  12. ITCS Test Strip Development and Certification

    Science.gov (United States)

    Carrigan, Caitlin; Adam, Niklas; Pickering, Karen; Gazda, Daniel; Piowaty, Hailey

    2011-01-01

    Internal coolant loops used for International Space Station thermal control must be periodically monitored for system health, including pH, biocide levels and any indication of ammonia. The presence of ammonia, possible via a microleak in the interface between the internal and external thermal control systems, could be a danger to the crew. The Internal Thermal Control System (ITCS) Sampling Kit uses test strips as a colorimetric indicator of pH and concentrations of biocide and free ammonia. This paper describes the challenges in designing an ammonia colorimetric indicator in a variable pH environment, as well as lessons learned, ultimately resulting in a robust test strip to indicate a hazardous ammonia leak.

  13. Energy-efficient recovery of butanol from model solutions and fermentation broth by adsorption.

    Science.gov (United States)

    Qureshi, N; Hughes, S; Maddox, I S; Cotta, M A

    2005-07-01

    This article discusses the separation of butanol from aqueous solutions and/or fermentation broth by adsorption. Butanol fermentation is also known as acetone butanol ethanol (ABE) or solvent fermentation. Adsorbents such as silicalite, resins (XAD-2, XAD-4, XAD-7, XAD-8, XAD-16), bone charcoal, activated charcoal, bonopore, and polyvinylpyridine have been studied. Use of silicalite appears to be the more attractive as it can be used to concentrate butanol from dilute solutions (5 to 790-810 g L(-1)) and results in complete desorption of butanol (or ABE). In addition, silicalite can be regenerated by heat treatment. The energy requirement for butanol recovery by adsorption-desorption processes has been calculated to be 1,948 kcal kg(-1) butanol as compared to 5,789 kcal kg(-1) butanol by steam stripping distillation. Other techniques such as gas stripping and pervaporation require 5,220 and 3,295 kcal kg(-1) butanol, respectively.

  14. A Spinning Particle in a Mobius Strip

    CERN Document Server

    Nieto, J A

    2011-01-01

    We develop the classical and quantum theory of a spinning particle moving in a Mobius strip. We first propose a Lagrangian for such a system and then we proceed to quantize the system via the constraint Hamiltonian system formalism. Our results may be of particular interest in several physical scenarios, including solid state physics and optics. In fact, the present work may shed some new light on the recent discoveries on condensed matter concerning topological insulators.

  15. Hot Strip Laminar Cooling Control Model

    Institute of Scientific and Technical Information of China (English)

    WANG Jun; WANG Guo-dong; LIU Xiang-hua

    2004-01-01

    The control model of laminar cooling system for hot strip, including air-cooling model, water-cooling model, temperature distribution model along thickness direction, feedforward control model, feedback control model and self-learning model, was introduced. PID arithmetic and Smith predictor controller were applied to feedback control. The sample of model parameter classification was given. The calculation process was shown by flow chart. The model has been proved to be simple, effective and of high precision.

  16. Mastering Interproximal Stripping: With Innovations in Slenderization

    OpenAIRE

    Sharma, Narendra Shriram; Shrivastav, Sunita S; Hazarey, Pushpa V

    2012-01-01

    ABSTRACT Crowding and irregularity remain a consistent problem for children. Management of space problems continues to play an important role in a dental practice. It also represents an area of major interaction between the primary provider and the specialists. Proximal stripping is routinely carried out to avoid extraction in borderline cases where space discrepancy is less and in cases where there is a discrepancy between the mesio- distal width of maxillary and mandibular teeth to satisfy ...

  17. Development of Silicon Multi-strip Detector

    Institute of Scientific and Technical Information of China (English)

    TanJilian; JinGenming; WangHongwei; YuanXiaohua; DuanLiming; LiSonglin; LuZiwei; XuHushan; NingBaojun; TianDayu; WangWei; ZhangLu

    2003-01-01

    Position sensitive detector is very important for nuclear physics experiment. There several techniques can be used to fabricate position sensitive detector, for example, Si-surface barrier method, diffusion method, ion implantation and planar process etc. Among all the techniques mentioned above planar process is the best one. We have developed batch of position sensitive detector -- silicon multi-strip detector by using planar process.

  18. Multitwist optical Möbius strips.

    Science.gov (United States)

    Freund, Isaac

    2010-01-15

    Circularly polarized Gauss-Laguerre GL00 and GL01 laser beams that cross at their waists at a small angle are shown to generate a quasi-paraxial field that contains a line of circular polarization, a C line, surrounded by polarization ellipses whose major and minor axes generate multitwist Möbius strips with twist numbers that increase with the distance from the C point.

  19. Sustainable Water and Energy in Gaza Strip

    Science.gov (United States)

    Hamdan, L.; Zarei, M.; Chianelli, R.; Gardner, E.

    2007-12-01

    Shortage of fresh water is a common problem in different areas of the world including the Middle East. Desalination of seawater and brackish water is the cheapest way to obtain fresh water in many regions. This research focuses on the situation in Gaza Strip where there is a severe shortage in the energy and water supply. The depletion of fresh water supplies and lack of wastewater treatments result in environmental problems. A solar powered cogeneration plant producing water and energy is proposed to be a suitable solution for Gaza Strip. Solar energy, using Concentrating Solar thermal Power (CSP) technologies, is used to produce electricity by a steam cycle power plant. Then the steam is directed to a desalination plant where it is used to heat the seawater to obtain freshwater. The main objective of this research is to outline a solution for the water problems in Gaza Strip, which includes a cogeneration (power and water) solar powered plant. The research includes four specific objectives: 1- an environmental and economic comparison between solar and fossil fuel energies; 2- technical details for the cogeneration plant; 3- cost and funding, 4- the benefits.

  20. High-Rate Capable Floating Strip Micromegas

    CERN Document Server

    Bortfeldt, Jonathan; Biebel, Otmar; Danger, Helge; Flierl, Bernhard; Hertenberger, Ralf; Lösel, Philipp; Moll, Samuel; Parodi, Katia; Rinaldi, Ilaria; Ruschke, Alexander; Zibell, André

    2015-01-01

    We report on the optimization of discharge insensitive floating strip Micromegas (MICRO-MEsh GASeous) detectors, fit for use in high-energy muon spectrometers. The suitability of these detectors for particle tracking is shown in high-background environments and at very high particle fluxes up to 60MHz/cm$^2$. Measurement and simulation of the microscopic discharge behavior have demonstrated the excellent discharge tolerance. A floating strip Micromegas with an active area of 48cm$\\times$50cm with 1920 copper anode strips exhibits in 120GeV pion beams a spatial resolution of 50$\\mu$m at detection efficiencies above 95%. Pulse height, spatial resolution and detection efficiency are homogeneous over the detector. Reconstruction of particle track inclination in a single detector plane is discussed, optimum angular resolutions below $5^\\circ$ are observed. Systematic deviations of this $\\mu$TPC-method are fully understood. The reconstruction capabilities for minimum ionizing muons are investigated in a 6.4cm$\\time...

  1. Wakes of ram pressure stripped disc galaxies

    CERN Document Server

    Roediger, E; Hoeft, M

    2006-01-01

    Spiral galaxies that move through the intracluster medium lose a substantial amount of their gas discs due to ram pressure stripping. The recent observations of NGC 4388 by Oosterloo & van Gorkom 2005 reveal a tail of stripped gas of ~ 100 kpc behind the source galaxy. We present first 3D hydrodynamical simulations of the evolution of such ram pressure stripped tails. We find that if the ICM wind does not vary significantly over a period of a few 100 Myr, subsonic galaxies produce a tail with regular features similar to a von-Karman vortex street. In this case, the tail widens systematically by about 45 kpc per 100 kpc distance behind the source galaxy. The widening rate is independent of the galaxy's inclination for a large range of inclinations. For supersonic galaxies, the tail is more irregular than for subsonic ones. The tail observed for NGC 4388 is narrower than the tails in our simulations. Reasons for this difference may be additional physical processes such as heat conduction or viscosity. In ad...

  2. Anodic stripping voltammetry enhancement by redox magnetohydrodynamics.

    Science.gov (United States)

    Clark, Emily A; Fritsch, Ingrid

    2004-04-15

    The effect of an external magnetic field on linear scan anodic stripping voltammetry (ASV) in solutions of 10(-6)-10(-7) M concentrations of lead, cadmium, and copper at mercury films on glassy carbon electrodes has been investigated. A high concentration of Hg(2+) was added to the analyte solution to induce a large cathodic current during the deposition step. Therefore, a large Lorentz force from the net flux of charge through the magnetic field resulted in convection due to magnetohydrodynamics. The faster delivery of analytes to the mercury film electrode during deposition caused an increase in the anodic stripping peaks. The effect of varying Hg(2+) concentrations (0-60 mM) and magnetic field strengths (0-1.77 T) on the enhancement of the stripping peaks was investigated. Enhancements as large as 129% for peak currents and 167% for peak areas were observed. An enhancement of approximately 100% was observed when 60 mM Fe(3+) replaced high concentrations of Hg(2+). This method of convection exhibits promise for small-volume ASV analysis with possible improved limits of detection and decreased preconcentration times.

  3. Regenerative adsorption distillation system

    KAUST Repository

    Ng, Kim Choon

    2013-12-26

    There is provided a regenerative adsorption distillation system comprising a train of distillation effects in fluid communication with each other. The train of distillation effects comprises at least one intermediate effect between the first and last distillation effects of the train, each effect comprising a vessel and a condensing tube for flow of a fluid therein. The system further comprises a pair of adsorption-desorption beds in vapour communication with the last effect and at least one intermediate effect, wherein the beds contain an adsorbent that adsorbs vapour from the last effect and transmits desorbed vapour into at least one of the intermediate effect.

  4. Controlled functionalisation of single-walled carbon nanotube network electrodes for the enhanced voltammetric detection of dopamine.

    Science.gov (United States)

    E, Sharel P; Miller, Thomas S; Macpherson, Julie V; Unwin, Patrick R

    2015-10-21

    Voltammetric studies of dopamine (DA) oxidation on pristine and acid-treated single-walled carbon nanotube (SWNT) network electrodes were undertaken in order to investigate both the effect of network density and acid treatment times on the voltammetric characteristics for DA oxidation and the susceptibility of the electrodes to fouling. Through careful control of catalysed chemical vapour deposition growth parameters, multiply interconnected and randomly oriented SWNT networks of two significantly different densities were grown (high density, HD, coverage ≫10 μm length of SWNT per μm(-2) and low density, LD, coverage = 5 (±1) μmSWNTμm(-2)). Acid treatment was performed to provide materials with different electrochemical properties and SWNT coverage, as determined by field emission-scanning electron microscopy, atomic force microscopy and micro-Raman spectroscopy. A high concentration of DA (100 μM) was deliberately employed to accelerate the fouling phenomenon associated with DA oxidation in order to evaluate the lifetime of the electrodes. HD pristine SWNT networks were found to promote more facile electron transfer (ET) and were less susceptible to blocking, compared to LD pristine SWNT networks. Acid treatment resulted in both a further enhancement of the ET rate and a reduction in susceptibility towards electrode fouling. However, lengthy acid treatment detrimentally affected ET, due to a decrease in network density and significant damage to the SWNT network structure. These studies highlight the subtle interplay between SWNT coverage and degree of acid functionalisation when seeking to achieve the optimal SWNT electrode for the voltammetric detection of DA.

  5. Indirect differential pulse voltammetric determination of aluminum by a pyrocatechol violet-modified electrode

    Energy Technology Data Exchange (ETDEWEB)

    Chen, G.; Bi, S.; Dai, L.; Cao, M.; Chen, Y. Wang, X. [Nanjing Univ. (China)

    1999-03-01

    Aluminum is one of the abundant elements in the earth`s crust. It has been considered to be a causative agent for various neurological disorders such as Alzheimer Senile, presenile dementia and amyotrophic lateral sclerosis. It is also very harmful to plants and aquatic organisms. Therefore, the determination of Al is very important. A Pyrocatechol Violet (PCV) modified electrode for the voltammetric determination of aluminum is reported. The modified electrode is simply prepared by dip-coating a pyrolytic graphite electrode in a NaAc-HAc buffer solution of PCV. Optimum experimental conditions for aluminum determination include a 0.2 mol/L NaAc-HAc buffer solution of pH 4.8, a PCV concentration of 0.02 mol/L used to modify the electrode and the use of differential-pulse mode for measurement. The peak currents of differential pulse voltammograms (DPV) decrease with the addition of Al into the buffer solution while the peak potentials remain the same. The decreasing value of peak current {Delta}i{sub p} is linear with Al concentration in the range of 1{times}10{sup {minus}8} to 1{times}10{sup {minus}7} mol/L and 1{times}10{sup {minus}7} to 1{times}10{sup {minus}6} mol/L. The detection limit is 5{times}10{sup {minus}9} mol/L and the relative standard deviation for 4{times}10{sup {minus}8} mol/L Al is 2.9% (n=8). The stability of this electrode is satisfactory. No serious interference is found. This method has been applied to determine Al in drinking water samples.

  6. Glyphosate Detection by Means of a Voltammetric Electronic Tongue and Discrimination of Potential Interferents

    Science.gov (United States)

    Bataller, Román; Campos, Inmaculada; Laguarda-Miro, Nicolas; Alcañiz, Miguel; Soto, Juan; Martínez-Máñez, Ramón; Gil, Luís; García-Breijo, Eduardo; Ibáñez-Civera, Javier

    2012-01-01

    A new electronic tongue to monitor the presence of glyphosate (a non-selective systemic herbicide) has been developed. It is based on pulse voltammetry and consists in an array of three working electrodes (Pt, Co and Cu) encapsulated on a methacrylate cylinder. The electrochemical response of the sensing array was characteristic of the presence of glyphosate in buffered water (phosphate buffer 0.1 mol·dm−3, pH 6.7). Rotating disc electrode (RDE) studies were carried out with Pt, Co and Cu electrodes in water at room temperature and at pH 6.7 using 0.1 mol·dm−3 of phosphate as a buffer. In the presence of glyphosate, the corrosion current of the Cu and Co electrodes increased significantly, probably due to the formation of Cu2+ or Co2+ complexes. The pulse array waveform for the voltammetric tongue was designed by taking into account some of the redox processes observed in the electrochemical studies. The PCA statistical analysis required four dimensions to explain 95% of variance. Moreover, a two-dimensional representation of the two principal components differentiated the water mixtures containing glyphosate. Furthermore, the PLS statistical analyses allowed the creation of a model to correlate the electrochemical response of the electrodes with glyphosate concentrations, even in the presence of potential interferents such as humic acids and Ca2+. The system offers a PLS prediction model for glyphosate detection with values of 098, −2.3 × 10−5 and 0.94 for the slope, the intercept and the regression coefficient, respectively, which is in agreement with the good fit between the predicted and measured concentrations. The results suggest the feasibility of this system to help develop electronic tongues for glyphosate detection. PMID:23250277

  7. Simultaneous voltammetric determination of tramadol and acetaminophen using carbon nanoparticles modified glassy carbon electrode

    Energy Technology Data Exchange (ETDEWEB)

    Ghorbani-Bidkorbeh, Fatemeh [Department of Chemistry, Sharif University of Technology, Tehran 11155-9516 (Iran, Islamic Republic of); Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Shahrokhian, Saeed, E-mail: shahrokhian@sharif.ed [Department of Chemistry, Sharif University of Technology, Tehran 11155-9516 (Iran, Islamic Republic of); Institute for Nanoscience and Technology, Sharif University of Technology, Tehran (Iran, Islamic Republic of); Mohammadi, Ali [Department of Drug and Food Control, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Dinarvand, Rassoul [Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of); Nanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, P.O. Box 14155-6451, Tehran (Iran, Islamic Republic of)

    2010-03-01

    A sensitive and selective electrochemical sensor was fabricated via the drop-casting of carbon nanoparticles (CNPs) suspension onto a glassy carbon electrode (GCE). The application of this sensor was investigated in simultaneous determination of acetaminophen (ACE) and tramadol (TRA) drugs in pharmaceutical dosage form and ACE determination in human plasma. In order to study the electrochemical behaviors of the drugs, cyclic and differential pulse voltammetric studies of ACE and TRA were carried out at the surfaces of the modified GCE (MGCE) and the bare GCE. The dependence of peak currents and potentials on pH, concentration and the potential scan rate were investigated for these compounds at the surface of MGCE. Atomic force microscopy (AFM) was used for the characterization of the film modifier and its morphology on the surface of GCE. The results of the electrochemical investigations showed that CNPs, via a thin layer model based on the diffusion within a porous layer, enhanced the electroactive surface area and caused a remarkable increase in the peak currents. The thin layer of the modifier showed a catalytic effect and accelerated the rate of the electron transfer process. Application of the MGCE resulted in a sensitivity enhancement and a considerable decrease in the anodic overpotential, leading to negative shifts in peak potentials. An optimum electrochemical response was obtained for the sensor in the buffered solution of pH 7.0 and using 2 muL CNPs suspension cast on the surface of GCE. Using differential pulse voltammetry, the prepared sensor showed good sensitivity and selectivity for the determination of ACE and TRA in wide linear ranges of 0.1-100 and 10-1000 muM, respectively. The resulted detection limits for ACE and TRA was 0.05 and 1 muM, respectively. The CNPs modified GCE was successfully applied for ACE and TRA determinations in pharmaceutical dosage forms and also for the determination of ACE in human plasma.

  8. Striatal dopamine terminals release serotonin after 5-HTP pretreatment: in vivo voltammetric data.

    Science.gov (United States)

    Stamford, J A; Kruk, Z L; Millar, J

    1990-05-07

    Peripheral administration of 5-hydroxytryptophan (5-HTP) to rats causes 'wet dog' shakes and a parallel elevation of brain serotonin (5-HT) levels. The increase in 5-HT concentration does not, however, correlate with the endogenous 5-HT innervation raising the possibility that some 5-HTP is decarboxylated in non-serotonergic cells. In the present study we used in vivo voltammetry to establish whether 5-HTP treatment led to formation of 5-HT as a 'false transmitter' in striatal dopamine (DA) neurons. Fast cyclic voltammetry at carbon fibre microelectrodes (CFMs) was used to monitor striatal monoamine release following electrical stimulation of the median forebrain bundle (MFB). In the absence of any pretreatment DA was the sole compound released by stimulation. However, when DA release was abolished with alpha-methyl-p-tyrosine (AMPT), 5-HTP administration (after peripheral decarboxylase inhibition) caused a dose-dependent release of 5-HT, confirmed by the voltammetric characteristics. Central decarboxylase inhibition prevented release indicating that 5-HTP itself was not released. By monitoring reduction peaks it was possible to record DA and 5-HT release simultaneously at a single CFM. While DA and 5-HT oxidised at the same potential their reduction peaks were separated by approximately 450 mV. It was shown, using this means, that 5-HT was still detectable even when DA release was not abolished by AMPT. DA and 5-HT release showed a significant positive correlation suggesting that they were released from the same nerves. We conclude that, after 5-HTP treatment, 5-HT can be released as a false transmitter from striatal DA neurones.

  9. Study of the voltammetric behaviour of metam and its application to an amperometric flow system.

    Science.gov (United States)

    Barroso, M Fátima; Paíga, Paula; Vaz, M Carmo V F; Delerue-Matos, Cristina

    2005-11-01

    The electrochemical behaviour of the pesticide metam (MT) at a glassy carbon working electrode (GCE) and at a hanging mercury drop electrode (HMDE) was investigated. Different voltammetric techniques, including cyclic voltammetry (CV) and square wave voltammetry (SWV), were used. An anodic peak (independent of pH) at +1.46 V vs AgCl/Ag was observed in MT aqueous solution using the GCE. SWV calibration curves were plotted under optimized conditions (pH 2.5 and frequency 50 Hz), which showed a linear response for 17-29 mg L(-1). Electrochemical reduction was also explored, using the HMDE. A well defined cathodic peak was recorded at -0.72 V vs AgCl/Ag, dependent on pH. After optimizing the operating conditions (pH 10.1, frequency 150 Hz, potential deposition -0.20 V for 10 s), calibration curves was measured in the concentration range 2.5 x 10(-1) to 1.0 mg L(-1) using SWV. The electrochemical behaviour of this compound facilitated the development of a flow injection analysis (FIA) system with amperometric detection for the quantification of MT in commercial formulations and spiked water samples. An assessment of the optimal FIA conditions indicated that the best analytical results were obtained at a potential of +1.30 V, an injection volume of 207 muL and an overall flow rate of 2.4 ml min(-1). Real samples were analysed via calibration curves over the concentration range 1.3 x 10(-2) to 1.3 mg L(-1). Recoveries from the real samples (spiked waters and commercial formulations) were between 97.4 and 105.5%. The precision of the proposed method was evaluated by assessing the relative standard deviation (RSD %) of ten consecutive determinations of one sample (1.0 mg L(-1)), and the value obtained was 1.5%.

  10. Voltammetric Determination of Prochlorperazine and Ethopropazine Using a Gold Electrode Modified with Decanethiol SAM

    Directory of Open Access Journals (Sweden)

    Baizhao Zeng

    2003-12-01

    Full Text Available The voltammetric behavior of prochlorperazine and ethopropazine at a decanethiol (DEC self-assembled monolayer (SAM modified gold electrode (DEC/Au has been studied. It was observed that prochlorperazine exhibited an anodic peak at about 0.60 V (vs SCE, while ethopropazine exhibited two anodic peaks at about 0.49 V and 0.58 V on DEC/Au in pH 10 sodium carbonate buffer. This was due to their different electrochemical oxidation mechanisms. In this case, the oxidation of prochlorperazine and ethopropazine included one 2e step and two 1e steps, respectively. In the presence of some reductants such as ascorbic acid, the oxidation products of them can catalyze the oxidation of the reductants and thus make the peaks grow. In addition, it was found that the SAM structure became not so compact when prochlorperazine and ethopropazine were present, resulting from their permeating in the SAM. Various conditions were optimized for their determination. Under the selected conditions (i.e. 0.080 M pH 10 sodium carbonate buffer; scan rate: 100 mV/s; accumulation potential: –0.4 V or 0 V; accumulation time: 60 s, the peak currents were linear to prochlorperazine concentration in the ranges of 0.1~2.0 μM and 5.0~50 μM, and linear with ethopropazine in the ranges of 10 nM~0.1 μM and 0.5~20 μM. The RSD was 4.28% for 8 successive measurements of 1.0 μM prochlorperazine. The influence of some coexistents was examined.

  11. Effect of boron on hot strips of low carbon steel produced by compact strip production

    Institute of Scientific and Technical Information of China (English)

    Hao Yu; Yonglin Kang

    2008-01-01

    The effect of boron on hot strips of low carbon steel produced by compact strip production (CSP) to reduce the strength to a certain degree was investigated, which is quite different from that of high-strength low alloy steel. The mechanical properties and microstructural evolution of the hot strip were studied using optical microscopy and tensile tests. By means of an electrolytic disso- lution technique and Thermo-Cal calculation, the precipitates containing boron were analyzed and detected. From the electron back- scattered diffraction analysis, it can be deciphered whether the microstructure has recrystallized or not. Furthermore, the effect of boron segregation on the recrystallization or non-recrystallization conditions can be distinguished. The segregation behavior of boron was investigated in boron-containing steel. The nonequilibrium segregation of boron during processing was discussed on the basis of the forming complexes with vacancies that migrate to the boundaries prior to annihilation, which was confirmed by the subsequent cold rolling with annealing experiments.

  12. Differential Pulse Anodic Stripping Voltammetry for Mercury Determination

    OpenAIRE

    2015-01-01

    In the present work voltammetric investigations have been performed on HgCl2 aqueous solutions prepared from a Cz 9024 reagent. Carbon paste electrode (CPE), eriochrome black T modified carbon paste electrode (MCPE/EBT) and KCl 1M as background electrolyte, were involved within the experimental procedures. Cyclic voltammetry (CV) has been performed in order to compare the behaviour of the two electrodes in both K3[Fe(CN)6] and mercury calibration aqueous solution. Differential pulse anodic st...

  13. A STUDY ON ADSORPTION AND DESORPTION BEHAVIORS OF 14C FROM A MIXED BED RESIN

    Directory of Open Access Journals (Sweden)

    SEUNG-CHUL PARK

    2014-12-01

    Full Text Available Spent resin waste containing a high concentration of 14C radionuclide cannot be disposed of directly. A fundamental study on selective 14C stripping, especially from the IRN-150 mixed bed resin, was carried out. In single ion-exchange equilibrium isotherm experiments, the ion adsorption capacity of the fresh resin for non-radioactive HCO3− ion, as the chemical form of 14C, was evaluated as 11mg-C/g-resin. Adsorption affinity of anions to the resin was derived in order of NO3− > HCO3− ≥ H2PO4−. Thus the competitive adsorption affinity of NO3− ion in binary systems appeared far higher than that of HCO3− or H2PO4−, and the selective desorption of HCO3− from the resin was very effective. On one hand, the affinity of Co2+ and Cs+ for the resin remained relatively higher than that of other cations in the same stripping solution. Desorption of Cs+ was minimized when the summation of the metal ions in the spent resin and the other cations in solution was near saturation and the pH value was maintained above 4.5. Among the various solutions tested, from the view-point of the simple second waste process, NH4H2PO4 solution was preferable for the stripping of 14C from the spent resin.

  14. Polarographic and Voltammetric Behavior of Cadmium(Ⅱ)-meso-tetrakis (p-sulfophenyl)porphyrin Complex%镉(Ⅱ)-meso(4-磺基苯)卟啉络合物的极谱伏安行为

    Institute of Scientific and Technical Information of China (English)

    王小萍; 张勇; 潘景浩

    2001-01-01

    The Polarographic and voltammetric behavior of Cd (Ⅱ)-meso-tetrakis(p-sulfophenyl)prophyrin (TPPS4) complex was defined and the cyclic voltammetric peak was obtained at 1.200 V (vs. SCE) in 0.3 mol/L NaoH solution. The characteristics of the peak have been examined in detail and the experimental results prove that the peak has adsorption properties. In addition to the number of electrons transferred in the reaction and the complex ratio, the stability const ant (β=1.19×107) was calculated. The peak current was proportional to the concentration of Cd (Ⅱ) over the rang 3×10-7~1×10-5 mol/L and the limit of detection was 6×10-8 mol/L. Furthermore a possible mechanism was proposed for the reduction of the complex.%用紫外分光光度法和循环伏安法考察了镉与meso(4-磺基苯)卟啉在强碱性溶液中形成的络合物的特性。结果表明,加入Cd(Ⅱ)后该卟啉的索瑞特(Soret)吸收带发生发红移,循环伏安图上出现了新的还原峰,峰电位为-1.20V(vs.SCE),络合物的络合比为1∶1,稳定常数β=1.19×107。本文还用多种电化学技术证明了络合物的还原峰电流具有吸附特征;用示波极谱法二阶导数波测试了峰电流与镉离子浓度的关系,结果表明镉离子在3×10-7~1×10-5mol/L的浓度范围内与络合物峰电流有良好的线性关系;并求得了电极反应的电子转移数为2。此外本文还对络合物的电极反应机理进行了探讨

  15. Evaluation of vermicompost as a raw natural adsorbent for adsorption of pesticide methylparathion.

    Science.gov (United States)

    Mendes, Camila Bitencourt; Lima, Giovana de Fátima; Alves, Vanessa Nunes; Coelho, Nívia Maria Melo; Dragunski, Douglas Cardoso; Tarley, César Ricardo Teixeira

    2012-01-01

    The assessment of vermicompost (VC) as a low-cost and alternative adsorbent for the removal of the pesticide methylparathion (MP) from an aqueous medium has been investigated by batch and column experiments. Parameters related to MP adsorption, i.e. equilibrium time (61.5 min) and adsorption pH (6.8) were optimized by using Doehlert design. The initial and final MP concentrations after adsorption assays were determined by square-wave adsorptive cathodic stripping voltammetry using an electrode composed of a multiwalled carbon nanotube dispersed in mineral oil. Batch adsorption experimental data were fitted to the Langmuir and Freundlich isotherm adsorptions, and a very good fit to the Langmuir linear model, giving a maximum adsorption capacity (MAC) of 0.17 mg g(-1). This result was very similar to that obtained with the column experiments. In order to evaluate the MP desorption from column packed VC, 100.0 ml of nitric acid solution (pH 3.0) has been percolated through material. No leaching of MP was observed, thus confirming the strong interaction between MP and VC. The satisfactory MAC obtained and low cost makes the VC a reliable natural material for the removal of MP from aqueous effluents.

  16. Improved voltammetric method for simultaneous determination of Pt and Rh using second derivative signal transformation - application to environmental samples.

    Science.gov (United States)

    Monteiro, Carlos E; Cobelo-Garcia, Antonio; Caetano, Miguel; Correia Dos Santos, Margarida M

    2017-12-01

    The determination of Platinum-group elements (PGE) in relevant environmental matrices is a challenging task. Sensitive and accurate analytical procedures for simultaneous determination of Pt and Rh are still needed. In this study, we report for the first time on the use of second derivative signal transformation to the ultra-trace simultaneous determination of Pt and Rh by Adsorptive Cathodic Stripping Voltammetry (AdCSV). With that step, the ill-defined peaks typically observed in the original voltammograms are transformed into well-shaped peaks, resulting in accurate detection. The experimental conditions were investigated and optimised: a suitable electrolyte for both elements, with less reagents consumption, (0.25M H2SO4, 0.05M HCl, 0.01M FA and 0.5mM HZ), deposition time (td) and deposition potential (Ed). For td = 120s and Ed = -0.75V, linear relationships r > 0.999 were obtained in the concentration range up to 5.8ngL(-1) (27 pM) for Pt and up to 3.4ngL(-1) (34 pM) for Rh. Limits of detection were 0.2ngL(-1) for Pt and 0.08ngL(-1) for Rh. Lower values can be achieved by increasing the deposition time. Limits of quantification, LOQ, calculated as 3 times LOD, were 0.5ngL(-1) for Pt and 0.2ngL(-1) for Rh. The sensitivity of Pt was affected by elevated Zn concentrations, whereas a minor effect was observed for Rh. However, Pt and Rh determinations were not influenced using the standard addition method. Precision as intermediate precision and expressed as relative standard deviation, based on Pt and Rh spiked solutions and digested road dust CRM BCR-723 was 17% and 20% for Pt and Rh, respectively. Recoveries of CRM were around 90% for both elements. The method was successfully applied in the simultaneous determination of Pt and Rh in sediments from Tagus estuary and, for the first time, dissolved Rh was determined in water samples of a waste water treatment plant. Application of this technique in a multidisciplinary approach will be a relevant contribution to

  17. Simultaneous Voltammetric Determination of Three Herbicides in Food and Water Samples with the Aid of Chemometrics

    Institute of Scientific and Technical Information of China (English)

    NI Yong-nian; WANG Lin; KOKOT Serge

    2009-01-01

    Differential pulse stripping voltammetry method(DPSV) was applied to the determination of three herbicides,ametryn,cyanatryn,and dimethametryn.It was found that their voltammograms overlapped strongly,and it is difficult to determine these compounds individually from their mixtures.With the aid of chemometrics,classical least squares(CLS),principal component regression(PCR) and partial least squares(PLS),voltammogram resolution and quantitative analysis of the synthetic mixtures of the three compounds were successfully performed.The proposed method was also applied to the analysis of some real samples with satisfactory results.

  18. Adsorption of organic layers over electrodeposited magnetite (Fe{sub 3}O{sub 4}) thin films

    Energy Technology Data Exchange (ETDEWEB)

    Cortes, M., E-mail: m.cortes@ub.ed [Electrodep, Departament de Quimica Fisica and Institut de Nanociencia i Nanotecnologia (IN2UB), Universitat de Barcelona, Marti i Franques 1, 08028 Barcelona (Spain); Gomez, E. [Electrodep, Departament de Quimica Fisica and Institut de Nanociencia i Nanotecnologia (IN2UB), Universitat de Barcelona, Marti i Franques 1, 08028 Barcelona (Spain); Sadler, J. [H.H. Wills Physics Laboratory, Royal Fort, Tyndall Avenue, Bristol BS8 1TL (United Kingdom); Valles, E. [Electrodep, Departament de Quimica Fisica and Institut de Nanociencia i Nanotecnologia (IN2UB), Universitat de Barcelona, Marti i Franques 1, 08028 Barcelona (Spain)

    2011-04-15

    Research highlights: {yields} Adherent low roughness magnetite films ranging from 80 nm to 3.75 {mu}m-thick were electrodeposited on Au/glass substrates under galvanostatic control. {yields} X-ray diffraction and magnetic measurements corroborates the purity of the electrodeposited magnetite. {yields} Both dodecanethiol and oleic acid are shown to adsorb on the magnetite prepared at low temperature, significantly inducing the hydrophobicity of the surface. {yields} Contact angle and voltammetric measurements, as well as XPS confirm the monolayers formation. - Abstract: The formation of monolayers of two organic compounds (oleic acid and dodecanethiol) over magnetite films was studied. Magnetite films ranging from 80 nm to 3.75 {mu}m-thick were electrodeposited on Au on glass substrates under galvanostatic control, with deposition parameters optimized for minimum surface roughness. Films were characterised by SEM and AFM, showing granular deposits with a low rms roughness of 5-40 nm measured over an area of 1 {mu}m{sup 2}. The growth rate was estimated by measuring cross-sections of the thin films. Pure magnetite with an fcc structure is observed in XRD diffractograms. The adsorption of both oleic acid and dodecanethiol on the magnetite films was tested by immersing them in ethanol solutions containing the organic molecules, for different deposition time, temperature and cleaning procedure. Monolayer formation in both cases was studied by contact angle and voltammetric measurements, as well as XPS.

  19. Carbonaceous materials for adsorptive refrigerators

    Science.gov (United States)

    Buczek, B.; Wolak, E.

    2012-06-01

    Carbon monoliths prepared from hard coal precursors were obtained. The porous structure of the monoliths was evaluated on the basis of nitrogen adsorption — desorption equilibrium data. The investigated monoliths have a well-developed microporous structure with significant specific surface area (S BET ). Equilibrium studies of methanol vapour adsorption were used to characterize the methanol adsorptive capacity that was determined using a volumetric method. The heat of wetting by methanol was determined in order to estimate the energetic effects of the adsorption process. The results of the investigations show that all monoliths exhibit high adsorption capacity and high heat of wetting with methanol.

  20. Electrochemical sensor for organophosphate pesticides and nerve agents using zirconia nanoparticles as selective sorbents.

    Science.gov (United States)

    Liu, Guodong; Lin, Yuehe

    2005-09-15

    An electrochemical sensor for detection of organophosphate (OP) pesticides and nerve agents using zirconia (ZrO2) nanoparticles as selective sorbents is presented. Zirconia nanoparticles were electrodynamically deposited onto the polycrystalline gold electrode by cyclic voltammetry. Because of the strong affinity of zirconia for the phosphoric group, nitroaromatic OPs strongly bind to the ZrO2 nanoparticle surface. The electrochemical characterization and anodic stripping voltammetric performance of bound OPs were evaluated using cyclic voltammetric and square-wave voltammetric (SWV) analysis. SWV was used to monitor the amount of bound OPs and provide simple, fast, and facile quantitative methods for nitroaromatic OP compounds. The sensor surface can be regenerated by successively running SWV scanning. Operational parameters, including the amount of nanoparticles, adsorption time, and pH of the reaction medium have been optimized. The stripping voltammetric response is highly linear over the 5-100 ng/mL (ppb) methyl parathion range examined (2-min adsorption), with a detection limit of 3 ng/mL and good precision (RSD = 5.3%, n = 10). The detection limit was improved to 1 ng/mL by using 10-min adsorption time. The promising stripping voltammetric performances open new opportunities for fast, simple, and sensitive analysis of OPs in environmental and biological samples. These findings can lead to a widespread use of electrochemical sensors to detect OP contaminates.

  1. Uranium stripping from tributyl phosphate by urea solutions

    Science.gov (United States)

    Skripchenko, S. Yu.; Titova, S. M.; Smirnov, A. L.; Rychkov, V. N.

    2016-09-01

    The process of uranium stripping from tri-n-butyl phosphate in kerosene by urea solutions was investigated at the volume ratio of the organic and aqueous phases of (1-10) : 1 in the temperature range of 20-60 °C. The stripping of uranium from a loaded organic phase increased with increasing urea content in the solution and with increasing temperature. Maximum recovery of uranium from tributyl phosphate was obtained using a solution that contained 8-12 mol/l of urea. The application of a urea solution for uranium stripping resulted in the strip product solution containing 200-240 g/L of uranium. The process of uranium stripping by dilute nitric acid was also investigated. Results of uranium stripping by the two methods are compared and discussed.

  2. High pressure water jet cutting and stripping

    Science.gov (United States)

    Hoppe, David T.; Babai, Majid K.

    1991-01-01

    High pressure water cutting techniques have a wide range of applications to the American space effort. Hydroblasting techniques are commonly used during the refurbishment of the reusable solid rocket motors. The process can be controlled to strip a thermal protective ablator without incurring any damage to the painted surface underneath by using a variation of possible parameters. Hydroblasting is a technique which is easily automated. Automation removes personnel from the hostile environment of the high pressure water. Computer controlled robots can perform the same task in a fraction of the time that would be required by manual operation.

  3. Fermilab silicon strip readout chip for BTev

    Energy Technology Data Exchange (ETDEWEB)

    Yarema, Raymond; Hoff, Jim; Mekkaoui, Abderrezak; Manghisoni, Massimo; Re, Valerio; Angeleri, Valentina; Manfredi, Pier Francesco; Ratti, Lodovico; Speziali, Valeria; /Fermilab /Bergamo U. /INFN, Pavia /Pavia U.

    2005-05-01

    A chip has been developed for reading out the silicon strip detectors in the new BTeV colliding beam experiment at Fermilab. The chip has been designed in a 0.25 {micro}m CMOS technology for high radiation tolerance. Numerous programmable features have been added to the chip, such as setup for operation at different beam crossing intervals. A full size chip has been fabricated and successfully tested. The design philosophy, circuit features, and test results are presented in this paper.

  4. Intelligent Control on Hot Strip Coiling Temperature

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    A new intelligent control scheme for hot strip coiling temperature is presented. In this scheme, the prediction model of finishing temperature and the presetting model of main cooling zone are establish based on BP neural network, the feed-forward open-loop control model of main cooling zone is constructed based on T-S fuzzy neural network, a new improved structure of T-S fuzzy neural network is developed, and the feedback close-loop control model of precision cooling zone is obtained based on fuzzy control. The effectiveness of the proposed scheme has been demonstrated by computer simulation with a satisfactory result.

  5. Gas Stripping in the Simulated Pegasus Galaxy

    Science.gov (United States)

    Mercado, Francisco Javier; Samaniego, Alejandro; Wheeler, Coral; Bullock, James

    2017-01-01

    We utilize the hydrodynamic simulation code GIZMO to construct a non-cosmological idealized dwarf galaxy built to match the parameters of the observed Pegasus dwarf galaxy. This simulated galaxy will be used in a series of tests in which we will implement different methods of removing the dwarf’s gas in order to emulate the ram pressure stripping mechanism encountered by dwarf galaxies as they fall into more massive companion galaxies. These scenarios will be analyzed in order to determine the role that the removal of gas plays in rotational vs. dispersion support (Vrot/σ) of our galaxy.

  6. Beam Test Results for MSGC's with Thick Metal Strips.

    CERN Document Server

    Beaumont, W; Bernier, K; Bouhali, O; Boulogne, I; Daubie, Evelyne; De Troy, J G; Delentdecker, G; Devroede, O; Gregoire,,; Iacopi, F; Udo, Fred; Van Doninck, W K; Van Dyck, C; Van Lancker, L; Van der Velde, C; Verbeure, F; Zhukov, V

    1999-01-01

    Micro Strip Gas Counters with robust gold strips have been developed at IMEC, the Interuniversity Microelectronics Center at Leuven, in Belgium. The electroless plating technology was used, allowing to achieve a strip thickness of up to 1.6 mu m on 10 X 10 cm**2 substrates. Results on signal to noise ratio, spark rate, resulting damages and detector occupancy are presented for counters exposed to various intensities of heavily ionizing particles.

  7. Study on Production of Rubber Sealing Strips with Steel Bones

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Rubber sealing strips with steel bones are used in car manufacturing that produced in large quantities. Cutting processes, such as milling and punching, are needed when the strips are produced. Accuracy, smoothness and flatness of the machined surface have to be guaranteed in the cutting process; moreover, deformation of the steel bone and peeling-off of the rubber must be avoided. Therefore cutting action of rubber/steel strips differs from that of rubber or metal workpiece separately. In this paper, milli...

  8. Time domain non linear strip theory for ship motions

    OpenAIRE

    Fan, Y.T.; Wilson, P. A.

    2004-01-01

    A new implementation of strip theory is proposed based on the strip theory by Salvesen, et al. [1] and early work by Westlake and Wilson [2]. Compared with traditional strip theory, the main difference is that the calculation is carried out in the time domain. This makes it possible to cope with relatively large-amplitude motions and non-constant forward speed problems. At each time step, the exact underwater sections are extracted; the velocity potential is required to satisfyt...

  9. Factors Influencing Bonding Strength of Laminated Bamboo Strips Lumber

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Factors influencing bonding strength of laminated bamboo strips lumber (LBSL) were investigated in this paper. In order to find an optimized technology, this paper investigated how the thickness of bamboo strips, the assembly orientation of bamboo curtain, the type of adhesives, as well as coupling agent treatment of bamboo curtain affected the bonding strength. The following conclusions were drawn: 1)The thinner the thickness of the bamboo strips, the bigger the bonding strength of LBSL; 2) The assembly or...

  10. Terminal Strip Facilitates Printed-Circuit Board Changes

    Science.gov (United States)

    Pinto, E. A.; Mcosker, C. E.

    1983-01-01

    Laminanted copper and polyimide terminal strip makes it easy to modify printed-circuit (PC) board, after board has been fabricated. When epoxied over conductors or insulating portion of PC board, strip provides series of solder-coated copper conductor pads to which integrated-circuit leads are soldered for functional changes. Terminal strips accommodate leads on dual inline IC package or as staggered single or multiple leads on planar mounted flatpacks.

  11. Space Vehicle Heat Shield Having Edgewise Strips of Ablative Material

    Science.gov (United States)

    Blosser, Max L. (Inventor); Poteet, Carl C. (Inventor); Bouslog, Stan A. (Inventor)

    2015-01-01

    A heat shield for a space vehicle comprises a plurality of phenolic impregnated carbon ablator (PICA) blocks secured to a surface of the space vehicle and arranged in a pattern with gaps therebetween. The heat shield further comprises a plurality of PICA strips disposed in the gaps between the PICA blocks. The PICA strips are mounted edgewise, such that the structural orientation of the PICA strips is substantially perpendicular to the structural orientation of the PICA blocks.

  12. Quantification of the Vasoactive Agent Buflomedil HCl in Pharmaceutical Formulation and Human Serum by Stripping Voltammetry and Liquid Chromatography.

    Science.gov (United States)

    El-Desoky, Hanaa S; Ghoneim, Mohamed M; Abdel-Galeil, Mohamed M

    2010-06-01

    Buflomedil HCl, was reduced at the mercury electrode in buffered solutions of various pH values (2-11) via a single 2-electron irreversible step corresponding to reduction of its C=O double bond. Buflomedil HCl has interfacial adsorptive behavior onto the mercury electrode surface and a monolayer surface coverage of 2.37 × 10-10 mol cm-2 was estimated. Each adsorbed buflomedil HCl molecule was found to occupy an area of 0.69 nm2 onto the HMDE surface. Differential-pulse (DP), liner-sweep (LS) and square-wave (SW) adsorptive cathodic stripping voltammetry (AdCSV) methods were described for its determination in the bulk form. The sensitivity of the described electro-analytical methods increases in the direction: DP-AdCSV voltammetry method is much more sensitive than the described chromatographic one. However the described chromatographic method is substantially simpler, faster and more sensitive than the previously reported HPLC methods.

  13. Clad strip casting by a twin roll caster

    OpenAIRE

    T. Haga; Nakamura, R; S. Kumai; H. Watari

    2009-01-01

    Purpose: Of this paper is to realize the casting of the clad strip by only one process. Therefore, the investigation of the ability of the casting of the clad strip by a vertical type twin roll caster was operated. The aim of the use of the twin roll caster to make clad strip was in the reduction of the production-energy of the clad strip.Design/methodology/approach: Used in the present study was a vertical type twin roll caster with the scriber. The scriber was used to prevent the mixture of...

  14. Three-Dimensional Model for Strip Hot Rolling

    Institute of Scientific and Technical Information of China (English)

    ZHANG Guo-min; XIAO Hong; WANG Chun-hua

    2006-01-01

    A three-dimensional model for strip hot rolling was developed, in which the plastic deformation of strip, the thermal crown of rolls, roll deflection and flattening were calculated by rigid-plastic finite element method, finite difference method, influential function method and elastic finite element method respectively. The roll wear was taken into consideration. The model can provide detailed information such as rolling pressure distribution, contact pressure distribution between backup rolls and work rolls, deflection and flattening of work rolls, lateral distribution of strip thickness, and lateral distribution of front and back tensions. The finish rolling on a 1 450 mm hot strip mill was simulated.

  15. Linear sweep voltammetric studies on the supramolecular complex of alizarin red S with lysozyme and determination of lysozyme

    Indian Academy of Sciences (India)

    Wei Sun; Na Zhao; Xueliang Niu; Yan Wang; Kui Jiao

    2009-03-01

    An electrochemical method for the determination of lysozyme (LYS) based on its interaction with alizarin red S (ARS) was established by linear sweep voltammetry in this paper. The electrochemical behaviour of ARS with LYS was investigated on a dropping mercury working electrode in 0.2 mol/L pH 4.8 Britton-Robinson (B-R) buffer solution. ARS showed a sensitive second order derivative linear sweep voltammetric reductive peak at -0.42 V (vs SCE). After the addition of LYS, the reductive peak current of ARS decreased without the shift of the reductive peak potential and no new waves appeared, which was due to the formation of a supramolecular complex of ARS with LYS in the solution. The stoichiometry of the ARS-LYS complex was further calculated by the electrochemical data with the results of the binding ratio as 3 : 1 and the binding constant as 2.82 × 1014. Under the selected conditions, the decrease of the second order derivative linear sweep voltammetric reductive peak current of ARS was in proportion to the LYS concentration in the range from 0.8 to 35.0 mg/L and the detection limit of LYS was calculated as 0.52 mg/L (3). Different kinds of LYS samples were detected satisfactorily with this method.

  16. Electroanalytical characteristics of piribedil and its differential pulse and square wave voltammetric determination in pharmaceuticals and human serum.

    Science.gov (United States)

    Uslu, Bengi; Ozkan, Sibel A

    2003-03-10

    The electrochemical oxidative behavior of piribedil (PR) was described. It was investigated by cyclic, linear sweep, differential pulse (DPV) and square wave (SWV) voltammetric techniques. The redox behavior of PR was found irreversible. Different parameters were tested to optimize the conditions for the determination of PR. The dependence of intensities of currents and potential on pH, concentration, scan rate, nature of the buffer was investigated. Two sensitive methods for the measurement of PR were described. For analytical purposes, a very well resolved diffusion controlled voltammetric peak was obtained in 0.1 M H(2)SO(4) and pH 5.7 acetate buffer. The determination peaks are obtained at 1.27 and 0.95 V for differential pulse and 1.29 and 0.97 V for SWV in 0.1 M H(2)SO(4) and pH 5.7 acetate buffer, respectively. The linear response was obtained in the ranges of 2 x 10(-6)-1 x 10(-3) M in 0.1 M H(2)SO(4) and 2 x 10(-6)-8 x 10(-4) M in pH 5.7 acetate buffer for both techniques. The proposed techniques were successfully applied to the determination of PR in tablet dosage forms and human serum. Excipients did not interfere in the determination. The necessary statistical validation reveals that the proposed methods are free from significant systematic errors.

  17. Voltammetric reduction of 4-nitroimidazole derivatives: Influence of the N-1 substitution in protic and aprotic media

    Energy Technology Data Exchange (ETDEWEB)

    Bollo, S.; Jara-Ulloa, P.; Zapata-Torres, G.; Cutino, E.; Sturm, J.C.; Nunez-Vergara, L.J. [Bioelectrochemistry Laboratory, Chemical and Pharmaceutical Sciences Faculty, University of Chile, Postal Code 838492 Santiago (Chile); Squella, J.A., E-mail: asquella@ciq.uchile.c [Bioelectrochemistry Laboratory, Chemical and Pharmaceutical Sciences Faculty, University of Chile, Postal Code 838492 Santiago (Chile)

    2010-06-01

    The voltammetric reduction of 1-methyl- and 1-H- 4-nitroimidazole derivatives was studied in different protic and aprotic media to investigate the influence of the N-1 substitution in the mechanism of reduction, the susceptibility of the nitro group to reduction, and the stability of the nitro radical anion. The elucidation of their voltammetric behavior was carried out using differential pulse polarography and cyclic voltammetry with two different mixed media (Britton-Robinson/ethanol: 70/30 and DMF/citrate: 60/40) and an aprotic media (DMF) at the mercury electrode. In addition, we used UV-vis spectroscopy for the study of their chemistry in solution and quantum-chemical calculations to evaluate LUMO energies, HOMO and LUMO energy gaps, dipole moments and electron affinity, using water and DMF as solvents. The mechanism of reduction was strongly dependent on both the substitution at the N-1 position and the nature of the media. In all media, the methyl-substituted derivative (M-4-NImOH) was always more easily reduced than the demethylated species (H-4-NImOH). On the other hand, the nitro radical anion from M-4-NImOH was more stable than the nitro radical anion from H-4-NImOH.

  18. Electrooxidative decarboxylation of vanillylmandelic acid: voltammetric differentiation between the structurally related compounds homovanillic acid and vanillylmandelic acid.

    Science.gov (United States)

    Li, Qian; Batchelor-McAuley, Christopher; Compton, Richard G

    2010-07-29

    Vanillylmandelic acid (VMA) and homovanillic acid (HVA) are the major end products of catecholamine metabolism. Abnoramally high levels in both plasma and urine may be indicative of a number of diseases including neuroblastoma and phaeochromocytoma. Commonly the VMA:HVA ratio is used as a disease marker, so that any measurement techniques need to be able to differentiate between these two structurally similar compounds. Electrochemistry is often limited in selectivity due to many organic molecules being oxidized or reduced at similar potentials. This work investigates the electrochemical oxidation mechanism of VMA at an edge-plane pyrolytic graphite electrode and highlights how, although structurally similar to HVA, their voltammetric responses may be differentiated through appropriate selection of the electrode material. The oxidation of VMA exhibits two clear peaks and the mechanism is shown to proceed through the decarboxylation of VMA to form vanillin, which is further oxidized resulting in the second peak. Modification of the electrode with a porous layer of multiwalled carbon nanotubes so as to change the mass transport to that of a thin layer system causes the voltammetric resolution between the two species to be enhanced. Differential pulse voltammetry is used to measure the limits of detection for VMA on an edge-plane pyrolytic graphite electrode and on commercially available multiwalled carbon nanotube screen printed electrode, with limits of detection of 1.7 and 1.0 microM, respectively. These limits of detection are well within the range of sensitivity required for clinical sample measurement.

  19. Stripped elliptical galaxies as probes of ICM physics: I. Tails, wakes, and flow patterns in and around stripped ellipticals

    CERN Document Server

    Roediger, E; Nulsen, P E J; Forman, W R; Machacek, M; Randall, S; Jones, C; Churazov, E; Kokotanekova, R

    2014-01-01

    (abridged) Elliptical cluster galaxies are successively stripped of their gaseous atmospheres due to their motion through the ICM. The stripped galactic gas forms a 'tail' in the galaxy's wake. Deep X-ray observations reveal the fine-structure of the gas tail and of the interface between galactic gas and ICM. This fine-structure depends on dynamic conditions (galaxy potential, initial gas contents, orbit in the host cluster), stripping stage (early infall, pre-/post-pericenter passage), and on the still ill-constrained ICM plasma properties (thermal conductivity, viscosity, magnetic field structure). In a series of papers, we aim at disentangling dynamic and plasma effects in order to use observed stripped ellipticals as probes of the ICM plasma properties. This first paper determines flow phases and flow patterns of successive gas stripping by means of hydrodynamical simulations. During quasi-steady stripping, the flow of ICM around the remnant atmosphere is similar to the flow around solid bodies, including...

  20. Therapeutic surfactant-stripped frozen micelles

    Science.gov (United States)

    Zhang, Yumiao; Song, Wentao; Geng, Jumin; Chitgupi, Upendra; Unsal, Hande; Federizon, Jasmin; Rzayev, Javid; Sukumaran, Dinesh K.; Alexandridis, Paschalis; Lovell, Jonathan F.

    2016-05-01

    Injectable hydrophobic drugs are typically dissolved in surfactants and non-aqueous solvents which can induce negative side-effects. Alternatives like `top-down' fine milling of excipient-free injectable drug suspensions are not yet clinically viable and `bottom-up' self-assembled delivery systems usually substitute one solubilizing excipient for another, bringing new issues to consider. Here, we show that Pluronic (Poloxamer) block copolymers are amenable to low-temperature processing to strip away all free and loosely bound surfactant, leaving behind concentrated, kinetically frozen drug micelles containing minimal solubilizing excipient. This approach was validated for phylloquinone, cyclosporine, testosterone undecanoate, cabazitaxel and seven other bioactive molecules, achieving sizes between 45 and 160 nm and drug to solubilizer molar ratios 2-3 orders of magnitude higher than current formulations. Hypertonic saline or co-loaded cargo was found to prevent aggregation in some cases. Use of surfactant-stripped micelles avoided potential risks associated with other injectable formulations. Mechanistic insights are elucidated and therapeutic dose responses are demonstrated.