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Journal articles on the topic 'Adsorptive stripping differential pulse voltammetry'

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Published: 4 June 2021

Last updated: 25 July 2025

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1

Karastogianni, Sophia, and Stella Girousi. "Electrochemical Behavior and Voltammetric Determination of a Manganese(II) Complex at a Carbon Paste Electrode." Analytical Chemistry Insights 11 (January 2016): ACI.S32150. http://dx.doi.org/10.4137/aci.s32150.

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Investigation of the electrochemical behavior using cyclic voltammetry and detection of [Mn2+(thiophenyl-2-carboxylic acid)2 (triethanolamine)] with adsorptive stripping differential pulse voltammetry. The electrochemical behavior of a manganese(II) complex [Mn2+(thiophenyl-2-carboxylic acid)2(triethanolamine)] (A) was investigated using cyclic and differential pulse voltammetry in an acetate buffer of pH 4.6 at a carbon paste electrode. Further, an oxidation-reduction mechanism was proposed. Meanwhile, an adsorptive stripping differential pulse voltammetric method was developed for the determ

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2

Shanmugam, Kumaran, Jiří Barek, and Jiří Zima. "Polarographic and Voltammetric Determination of Submicromolar Concentrations of Genotoxic 1,5-Dinitronaphthalene." Collection of Czechoslovak Chemical Communications 69, no. 11 (2004): 2021–35. http://dx.doi.org/10.1135/cccc20042021.

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Polarographic and voltammetric behavior of 1,5-dinitronaphthalene was investigated using tast polarography and differential pulse polarography at a classic dropping mercury electrode and differential pulse voltammetry and adsorptive stripping voltammetry at a hanging mercury drop electrode. Optimum conditions have been found for the determination of tested substance in the concentration range 2-10 μmol l-1 in tast polarography, 0.2-1 μmol l-1 in differential pulse polarography at a classic dropping mercury electrode or differential pulse voltammetry at a hanging mercury drop electrode, and 0.0

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3

Ghoneim, M. M., M. A. El-Attar, and S. A. Razeq. "Voltammetric quantitation at the mercury electrode of the anticholinergic drug flavoxate hydrochloride in bulk and in a pharmaceutical formulation." Open Chemistry 5, no. 2 (2007): 496–507. http://dx.doi.org/10.2478/s11532-007-0011-2.

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AbstractFlavoxate hydrochloride, 2-piperidinoethyl 3-methyl-4-oxo-2-phenyl-4-H-chromene-8-carboxylate, is a smooth muscle antispasmodic. Its electrochemical behavior was studied at the mercury electrode in buffered solutions containing 30% (v/v) methanol using dc-polarography, differential-pulse polarography, cyclic voltammetry, and linear sweep-and square-wave adsorptive stripping voltammetry. Sensitive and precise procedures were developed for determination of bulk flavoxate hydrochloride and in the pharmaceutical formulation Genurin® S.F, without sample pretreatment or extraction. Limits of

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4

Gratteri, P., S. Pinzauti, E. La Porta, G. Papeschi, V. Cavrini, and G. Santoni. "Differential-pulse adsorptive stripping voltammetry of chlorhexidine." Analyst 116, no. 7 (1991): 723. http://dx.doi.org/10.1039/an9911600723.

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5

MAHMOUD, A. GANDOUR, ENSAF-ABOUL-KASIM, H. AMRALLAH A., and A. FARGHALY O. "Differential Pulse Polarography and Adsorptive Stripping Voltammetric Determination of Uric Acid." Journal of Indian Chemical Society Vol. 69, Dec 1992 (1992): 813–18. https://doi.org/10.5281/zenodo.6101088.

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Chemistry Department, Faculty of Science, Atsiut, Egypt Chemistry Department, Faculty of Science, Aswan, Egypt <em>Manuscript received 15 June 1992, accepted 1 September 1992</em> The complex formation between uric acid and zinc, cadmium and lead ions bas been investigated using differential pulse polarography in 0.01 <em>M</em> NaNO<sub>3</sub>. The complexes formed by Cd<sup>II</sup> and Pb<sup>lI</sup> with uric acid have the stoichiometry of 1 : 2. Zn<sup>ll</sup> does not give any indication of complexation with uric acid. A sensitive voltammetric method is developed for the qua

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6

MAHMOUD, A. GANDOUR, ENSAF-ABOUL·KASIM, H. AMRALLAH A., and A. FARGHALY 0. "Differential Pulse Polarography and Adsorptive Stripping Voltammetric Determination of Uric Acid." Journal Of Indian Chemical Society Vol. 69, Dec 1992 (1992): 813–18. https://doi.org/10.5281/zenodo.6031636.

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Chemistry Department, Faculty of Science, Assiut, Egypt Chemistry Department, Faculty of Science, Aswan, Egypt <em>Manuscript received 15 June 1992, accepted 1 September 1992</em> The complex formation between uric acid and zinc, cadmium and lead ions has been investigated using differential pulse polarography in 0.01 <em>M </em>NaNO<sub>3</sub>. The complexes formed by Cd<sup>II</sup> and Pb<sup>II</sup> with uric acid have the stoichiometry of 1 : 2. Zn<sup>II</sup> does not give any indication of complexation with uric acid. A sensitive voltammetric method is developed for the quantita

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7

Jemelková, Zuzana, Jiří Zima, and Jiří Barek. "Voltammetric and amperometric determination of doxorubicin using carbon paste electrodes." Collection of Czechoslovak Chemical Communications 74, no. 10 (2009): 1503–15. http://dx.doi.org/10.1135/cccc2009081.

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Direct current voltammetric (DCV) and differential pulse voltammetric (DPV) determination of antineoplastic agent doxorubicin (DOX) at a carbon paste electrode (CPE) was developed. Britton–Robinson buffer (pH 7.0) was used as a supporting electrolyte. The limits of detection are 8 × 10–7 mol l–1 (DCV) and 6 × 10–8 mol l–1 (DPV). The accumulation of DOX at the electrode surface was used to decrease the limits of detection down to 2.2 × 10–7 mol l–1 for adsorptive stripping DC voltammetry (DCAdSV) and 2.8 × 10–9 mol l–1 for adsorptive stripping differential pulse voltammetry (DPAdSV) at CPE. The

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8

Barek, Jiří, Jiří Zima, Josino C. Moreira, and Alexandr Muck. "Polarographic and Voltammetric Determination of 1-Nitropyrene." Collection of Czechoslovak Chemical Communications 65, no. 12 (2000): 1888–96. http://dx.doi.org/10.1135/cccc20001888.

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The polarographic behaviour of 1-nitropyrene was investigated by tast polarography, differential pulse polarography (both with a dropping mercury electrode), differential pulse voltammetry, and adsorptive stripping voltammetry (both with a hanging mercury drop electrode). Optimum conditions have been found for its determination by the given methods in the concentration ranges 2-100, 0.2-100, 0.1-10, and 0.001-0.01 μmol l-1, respectively.

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9

Thị Hue, Nguyen, Nguyen Van Hop, Hoang Thai Long, et al. "Determination of Chromium in Natural Water by Adsorptive Stripping Voltammetry Using In Situ Bismuth Film Electrode." Journal of Environmental and Public Health 2020 (May 14, 2020): 1–15. http://dx.doi.org/10.1155/2020/1347836.

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Development of adsorptive stripping voltammetry (AdSV) combined with in situ prepared bismuth film electrode (in situ BiFE) on glassy carbon disk surface using diethylenetriamine pentaacetic acid (DTPA) as a complexing agent and NO3− as a catalyst to determine the trace amount of chromium (VI) is demonstrated. According to this method, in the preconcentration step at Edep = −800 mV, the bismuth film is coated on the surface of glassy carbon electrodes simultaneously with the adsorption of complexes Cr(III)-DTPA. In addition to the influencing factors, the stripping voltammetry performance fact

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10

Kingsley, Mal Phebe, Pramod K. Kalambate, and Ashwini K. Srivastava. "Simultaneous determination of ciprofloxacin and paracetamol by adsorptive stripping voltammetry using copper zinc ferrite nanoparticles modified carbon paste electrode." RSC Advances 6, no. 18 (2016): 15101–11. http://dx.doi.org/10.1039/c5ra19861e.

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Development of copper zinc ferrite nanoparticles modified carbon paste electrode for the simultaneous determination of ciprofloxacin and paracetamol using adsorptive stripping differential pulse voltammetry.

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11

Amal, M. Abou Al Alamein Hassan A. M. Hendawy Nourhan O. ElABD* Maissa Y. Salem. "ELECTROCHEMICAL BEHAVIOUR OF TROMANTADINE HYDROCHLORIDE AT DIFFERENT ELECTRODES AND ITS ANALYTICAL APPLICATIONS." iajps,csk publications 03, no. 12 (2017): 1611–23. https://doi.org/10.5281/zenodo.260124.

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A simple, sensitive, rapid and precise method was developed using voltammetric techniques namely; cyclic voltammetry, differential pulse and square wave voltammetry for the determination of Tromantadine Hydrochloride (TH) at three different working electrodes namely; glassy carbon (GCE), carbon paste (CPE) and pencil graphite (PGE) electrodes. Firstly, we began with cyclic voltammetric analyses to optimize the voltammetric conditions. TH cyclic voltammogram revealed a well-defined irreversible anodic peak at about 0.751 V, 0.692 V and 0.784 V at GCE, CPE and PGE, respectively. The oxidation pr

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12

Billová, Sabina, René Kizek, and Emil Paleček. "Differential pulse adsorptive stripping voltammetry of osmium-modified peptides." Bioelectrochemistry 56, no. 1-2 (2002): 63–66. http://dx.doi.org/10.1016/s1567-5394(02)00008-7.

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13

Suciu, Pompilia, Marisol Vega, and Liviu Roman. "Determination of cadmium by differential pulse adsorptive stripping voltammetry." Journal of Pharmaceutical and Biomedical Analysis 23, no. 1 (2000): 99–106. http://dx.doi.org/10.1016/s0731-7085(00)00279-x.

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14

Ignjatović, Ljubiša M., Jiří Barek, Jiří Zima, and Milica C. Stević. "Adsorptive Stripping Voltammetric Determination of 1,1-Dimethyl-3-phenyltriazene." Collection of Czechoslovak Chemical Communications 73, no. 1 (2008): 97–106. http://dx.doi.org/10.1135/cccc20080097.

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The optimum conditions were found for the determination of 1,1-dimethyl-3-phenyltriazene in the concentration range from 1 × 10-4 to 1 × 10-7 mol l-1 by differential pulse voltammetry at a hanging mercury drop electrode. The sensitivity of the determination can be improved by preliminary adsorptive accumulation of the substance on the surface of the hanging mercury drop. Differential pulse adsorptive stripping voltammetry can be used for the purpose in the concentration range from 1 × 10-6 to 1 × 10-9 mol l-1. The determination limit is 1 × 10-9 mol l-1 for a deposition time of 10 min, the rel

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15

Hammam, E., H. S. El-Desoky, K. Y. El-Baradie, and A. M. Beltagi. "Three validated stripping voltammetric procedures for determination of the anti-prostate cancer drug flutamide in tablets and human serum at a mercury electrode." Canadian Journal of Chemistry 82, no. 9 (2004): 1386–92. http://dx.doi.org/10.1139/v04-104.

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Flutamide is a nonsteriodal anti-androgen drug, which is commonly used in the treatment of advanced prostate cancer. Based on the reduction of the nitro organic moiety of the drug molecule in acetate buffer of pH 5 at the hanging mercury drop electrode, three adsorptive cathodic stripping voltammetric procedures were optimized for determination of flutamide in bulk, tablets, and human serum applying linear-sweep, differential-pulse, and square-wave waveforms. The achieved limits of detection of the bulk drug were 1.9 × 107, 8.7 × 108, and 9.7 × 109 mol L1 by using the optimized differentia

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16

Ungureanu, Eleonora-Mihaela, Mariana Popescu (Apostoiu), Georgiana-Luiza Tatu (Arnold), et al. "Electrochemical Comparison on New (Z)-5-(Azulen-1-Ylmethylene)-2-Thioxo-Thiazolidin-4-Ones." Symmetry 13, no. 4 (2021): 588. http://dx.doi.org/10.3390/sym13040588.

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Three (Z)-5-(azulen-1-ylmethylene)-2-thioxo-thiazolidin-4-ones are electrochemically characterized by cyclic voltammetry, differential pulse voltammetry, and rotating disk electrode voltammetry. The electrochemical investigations revealed that the redox potential is influenced by the number and position of the alkyl groups, and the possible oxidation mechanism is proposed. These compounds, after their immobilization on glassy carbon electrodes during oxidative electropolymerization, were examined as complexing ligands for heavy metal ions from aqueous solutions through adsorptive stripping vol

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17

Pardi, Hilfi, and Nancy Willian. "Penentuan Logam Cr(VI) Menggunakan Metoda Differensial Pulse Adsorptive Stripping Voltammetry dengan Calconcarboxylic Acid Sebagai Pengomplek." Journal of The Indonesian Society of Integrated Chemistry 11, no. 2 (2019): 49–56. http://dx.doi.org/10.22437/jisic.v11i2.7858.

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[Determination of Cr(VI) Metal Using Differential Pulse Adsorptive Stripping Voltametry Method with Calconcarboxylic Acid as Complexing] Penelitian ini menggunakan metode differential pulse adsorptive stripping voltammetry (DPAdSV) dengan elektroda merkuri tetesan gantung (HMDE) untuk menentukan logam Cr(VI) dengan Calconcarboxylic Acid (CCA) sebagai ligand dalam sampel air laut. Metode ini terjadi berdasarkan deposisi Logam-CCA pada elektroda merkuri pada periode waktu tertentu. Dengan menggunakan scan potensial kearah negatif dan voltammogram differential pulse akan menghasilkan voltam

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18

Attar, Tarik, Yahia Harek, and Lahcene Larabi. "Determination of copper in whole blood by differential pulse adsorptive stripping voltammetry." Mediterranean Journal of Chemistry 2, no. 6 (2014): 691–700. http://dx.doi.org/10.13171/mjc.2.6.2014.21.02.25.

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Â 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

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19

Navalón, A., R. Blanc, L. Reyes, N. Navas, and J. L. Vílchez. "Determination of the antibacterial enrofloxacin by differential-pulse adsorptive stripping voltammetry." Analytica Chimica Acta 454, no. 1 (2002): 83–91. http://dx.doi.org/10.1016/s0003-2670(01)01524-0.

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20

Vı́lchez, José Luis, Jalila Taoufiki, Lilia Araujo, and Alberto Navalón. "Determination of the antibacterial trovafloxacin by differential-pulse adsorptive stripping voltammetry." Journal of Pharmaceutical and Biomedical Analysis 31, no. 3 (2003): 465–71. http://dx.doi.org/10.1016/s0731-7085(02)00713-6.

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21

Hernandez, Lucas, Pedro Hernandez, Encarnacion Lorenzo, Claudio Gonzalez, and Inmaculada Gonzalez. "Determination of Bentazepam by differential pulse polarography and adsorptive stripping voltammetry." Fresenius' Journal of Analytical Chemistry 336, no. 3 (1990): 222–25. http://dx.doi.org/10.1007/bf00332257.

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22

Goicolea, M. A., J. F. Arranz, R. J. Barrio, and Z. Gómez de Balugera. "Differential-pulse adsorptive stripping voltammetry of the herbicides metamitron and isometiozine." Fresenius' Journal of Analytical Chemistry 339, no. 3 (1991): 166–68. http://dx.doi.org/10.1007/bf00324404.

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23

Jaber, A. M. Y., and A. Lounici. "Adsorptive differential-pulse stripping voltammetry of norfloxacin and its analytical application." Analyst 119, no. 11 (1994): 2351. http://dx.doi.org/10.1039/an9941902351.

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24

Preda, Daniel, Gabriel Lucian Radu, Emilia-Elena Iorgulescu, Mihaela-Carmen Cheregi, and Iulia Gabriela David. "Curcumin-Based Molecularly Imprinted Polymer Electropolymerized on Single-Use Graphite Electrode for Dipyridamole Analysis." Molecules 29, no. 19 (2024): 4630. http://dx.doi.org/10.3390/molecules29194630.

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A new molecularly imprinted polymer (MIP)-based disposable electrochemical sensor for dipyridamole (DIP) determination was obtained. The sensor was rapidly prepared by potentiodynamic electrochemical polymerization on a pencil graphite electrode (PGE) using curcumin (CUR) as a functional monomer and DIP as a template molecule. After the optimization of the conditions (pH, monomer–template ratio, scan rate, number of cyclic voltammetric cycles applied in the electro-polymerization process and extraction time of the template molecule) for MIP formation, DIP voltammetric behavior at the modified

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25

Agrahari, Sunil K., Sangita D. Kumar, and Ashwini K. Srivastava. "Development of a Carbon Paste Electrode Containing Benzo-15-Crown-5 for Trace Determination of the Uranyl Ion by Using a Voltammetric Technique." Journal of AOAC INTERNATIONAL 92, no. 1 (2009): 241–47. http://dx.doi.org/10.1093/jaoac/92.1.241.

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Abstract The interaction of macrocyclic compounds like crown ethers and UO22+ has been studied by electrochemical methods. A modified carbon paste electrode incorporating benzo-15-crown-5 (B15C5) was used to evaluate the electron transfer reaction of UO22+ by cyclic voltammetry, differential pulse voltammetry, and electrochemical impedance spectroscopy. Electrochemical impedance studies showed that charge transfer resistance was less for the B15C5-modified electrode than for the plain carbon paste electrode (PCPE). On the basis of these observations, a UO22+-sensitive crown ether chemically mo

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26

Němcová, Lenka, Jiří Zima, and Jiří Barek. "Determination of 5-amino-6-nitroquinoline at a carbon paste electrode." Collection of Czechoslovak Chemical Communications 74, no. 10 (2009): 1477–88. http://dx.doi.org/10.1135/cccc2009065.

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Differential pulse voltammetry, direct current voltammetry, adsorptive stripping voltammetry and HPLC with electrochemical detection were used for the determination of 5-amino-6-nitroquinoline at a carbon paste electrode. The methods are based either on anodic oxidation or cathodic reduction of this substance, whose electrochemical behavior at carbon paste electrode was further studied by cyclic voltammetry. Practical applicability of these methods was demonstrated on the determination of 5-amino-6-nitroquinoline in model samples of drinking and river water. The detection limit was 2.0 × 10–6

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27

Saini, Ram Lal, Seema Parveen, Rajni Bais, Om Prakash, and Anurag Choudhary. "Cyclic Voltammetric determination of an antidepressant drug (Duloxetine hydrochloride) by using glassy carbon electrodes in bulk form and human biological fluids." Research Journal of Chemistry and Environment 26, no. 6 (2022): 48–64. http://dx.doi.org/10.25303/2606rjce048064.

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Duloxetine hydrochloride was measured by employing Differential Pulse Cathodic Adsorptive Stripping Voltammetry (DP-CAdSV) and Square Wave Cathodic Adsorptive Stripping Voltammetry at the glassy carbon electrode (GCE) in bulk form and human biological fluids. Duloxetine hydrochloride exhibited one distinct and well-defined cathodic peak in the potential range -0.80 to -0.85 V v/s Ag/AgCl/KCl reference electrode. Cyclic Voltammetry, DP-CAdSV and SW-CAdSV showed one reduction wave with peak potential -0.85 V at pH 7. The proposed method's excellent sensitivity was demonstrated by the obtained LO

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28

David, Iulia Gabriela, Nimet Numan, Mihaela Buleandră, et al. "Rapid Voltammetric Screening Method for the Assessment of Bioflavonoid Content Using the Disposable Bare Pencil Graphite Electrode." Chemosensors 9, no. 11 (2021): 323. http://dx.doi.org/10.3390/chemosensors9110323.

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Hesperidin (HESP) is a plant bioflavonoid found in various nutritional and medicinal products. Many of its multiple health benefits rely on the compound’s antioxidant ability, which is due to the presence of oxidizable hydroxyl groups in its structure. Therefore, the present study aimed to investigate the electrochemical behavior of HESP at a cheap, disposable pencil graphite electrode (PGE) in order to develop rapid and simple voltammetric methods for its quantification. Cyclic voltammetric investigations emphasized a complex electrochemical behavior of HESP. The influence of the electrode ma

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29

Alonso, Rosa M., Rosa M. Jimenez, and Arnold G. Fogg. "Differential-pulse adsorptive stripping voltammetry of the psychotropic drugs triazolam and clotiazepam." Analyst 113, no. 1 (1988): 27. http://dx.doi.org/10.1039/an9881300027.

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30

Altinoz, Sacide, Aytekin Temizer, and Sinan Beksac. "Determination of ceftriaxone in biological material by differential-pulse adsorptive stripping voltammetry." Analyst 115, no. 6 (1990): 873. http://dx.doi.org/10.1039/an9901500873.

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31

Nikolic, Katarina, Mara Aleksic, Vera Kapetanovic, and Danica Agbaba. "Voltammetric and theoretical studies of electrochemical behavior of cephalosporins at the mercury electrode." Journal of the Serbian Chemical Society 80, no. 8 (2015): 1035–49. http://dx.doi.org/10.2298/jsc150129019n.

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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 dens

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32

Lorenzetti, Anabela S., Tania Sierra, Claudia E. Domini, Adriana G. Lista, Agustin G. Crevillen, and Alberto Escarpa. "Electrochemically Reduced Graphene Oxide-Based Screen-Printed Electrodes for Total Tetracycline Determination by Adsorptive Transfer Stripping Differential Pulse Voltammetry." Sensors 20, no. 1 (2019): 76. http://dx.doi.org/10.3390/s20010076.

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Disposable electrochemically reduced graphene oxide-based (ERGO) screen-printed electrodes (SPE) were developed for the determination of total tetracyclines as a sample screening approach. To this end, a selective adsorption-detection approach relied on adsorptive transfer stripping differential pulse voltammetry (AdTDPV) was devised, where the high adsorption capacity and the electrochemical properties of ERGO were simultaneously exploited. The approach was very simple, fast (6 min.), highly selective by combining the adsorptive and the electrochemical features of tetracyclines, and it used j

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33

Hoang, Vu Dang, Dao Thi Huyen, and Phan Hong Phuc. "Adsorptive Cathodic Stripping Voltammetric Determination of Cefoperazone in Bulk Powder, Pharmaceutical Dosage Forms, and Human Urine." Journal of Analytical Methods in Chemistry 2013 (2013): 1–8. http://dx.doi.org/10.1155/2013/367914.

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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

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34

Piech, Robert, Ewa Niewiara, Beata Paczosa-Bator, and Marek Szlósarczyk. "The determination of molybdenum in selected mushrooms by stripping voltammetry." Open Chemistry 9, no. 2 (2011): 352–56. http://dx.doi.org/10.2478/s11532-011-0011-0.

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AbstractThe highly sensitive method of adsorptive stripping voltammetry (AdSV), with differential pulse steps, was performed at a mercury film electrode and has been applied here for the determination of trace molybdenum content in selected wild mushrooms. Fruiting body caps of 12 selected macrofungi species from Basidiomycetes have been investigated. Molybdenum content of investigated samples was determined in the range of 0.006 to 0.38 mg kg−1 of dry matter. The highest value of molybdenum content was found in Leccinum rufum and the lowest in Lactarius deliciosus.

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35

Preda, Daniel, Maria Lorena Jinga, Iulia Gabriela David, and Gabriel Lucian Radu. "Determination of Dipyridamole Using a MIP-Modified Disposable Pencil Graphite Electrode." Chemosensors 11, no. 7 (2023): 400. http://dx.doi.org/10.3390/chemosensors11070400.

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A new method for the determination of the antiplatelet drug dipyridamole (DIP) in pharmaceuticals using a molecularly imprinted polymer (MIP)-modified pencil graphite electrode (PGE) is proposed. The modified electrode was prepared simply and rapidly by electropolymerization of caffeic acid (CA) in the presence of DIP and subsequent DIP extraction with ethanol, resulting in a cost-effective, eco-friendly disposable modified electrode (MIP_PGE). Several working conditions (monomer and template concentration, number of voltametric cycles, scan rate extraction time, and solvent) for the MIP_PGE p

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36

Valarmathi, Munirathinam, Anandhan Gomathi, and Paramasivam Manisankar. "Development of Multiwalled Carbon Nanotube Based Electrochemical Sensor for Reactive Azo Dyes." Advanced Materials Research 678 (March 2013): 321–25. http://dx.doi.org/10.4028/www.scientific.net/amr.678.321.

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Two reactive azo dyes Reactive yellow 84 (RY84) and Reactive Red 120 (RR120) were investigated voltammetrically using plain glassy carbon electrode (GCE) and multiwalled carbon nanotube modified GCE (MWCNT/GCE). Influence of pH, scan rate and concentration on voltammograms were studied. The irreversible oxidation process observed for both dyes was adsorption controlled. The surface characterization of the modified electrode in the absence and presence of dyes was done using scanning electron microscopy (SEM). A systematic study of the experimental parameters that affects differential pulse str

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37

Barek, Jiří, Jaroslav Matějka, and Jiří Zima. "Determination of Acridine, Benz[c]acridine and Dibenz[a,h]acridine by Fast Scan Differential Pulse Voltammetry and Adsorptive Stripping Voltammetry." Collection of Czechoslovak Chemical Communications 59, no. 2 (1994): 294–308. http://dx.doi.org/10.1135/cccc19940294.

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The behaviour of the title compounds in fast scan differential pulse voltammetry and adsorptive stripping voltammetry was studied and the optimum conditions were found for their determination by FS DPV over the concentration region of (2 - 100) .10-7 mol l-1 and by AdSV over the concentration regions of (2 - 10) .10-8 mol l-1 for acridine and dibenz[a,h]acridine and (2 - 100) .10-9 mol l-1 for benz[c]acridine. Practical applicability of the methods to the monitoring of the chemical efficiency of destruction of the carcinogens with potassium permanganate was tested.

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38

Hao, Zhang, J.-C. Vire, G. J. Patriarche, and R. Wollast. "Determination of Cobalt Ions in Natural Waters Using Differential Pulse Adsorptive Stripping Voltammetry." Analytical Letters 21, no. 8 (1988): 1409–24. http://dx.doi.org/10.1080/00032718808059873.

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39

Alonso, Rosa M., Blanca Gallo, and Arnold G. Fogg. "Differential-pulse adsorptive stripping voltammetry of 3-(4,5-dimethyl-2-thiazolylazo)-2,6-diaminopyridine." Analyst 112, no. 11 (1987): 1611. http://dx.doi.org/10.1039/an9871201611.

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40

Ashournia, Mehdi, and Alireza Aliakbar. "Determination of selenium in natural waters by adsorptive differential pulse cathodic stripping voltammetry." Journal of Hazardous Materials 168, no. 1 (2009): 542–47. http://dx.doi.org/10.1016/j.jhazmat.2009.02.070.

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41

Passamonti, P., V. Bartocci, and F. Pucciarelli. "Determination of Captropril using adsorptive cathodic differential pulse stripping voltammetry with the HMDE." Journal of Electroanalytical Chemistry and Interfacial Electrochemistry 230, no. 1-2 (1987): 99–108. http://dx.doi.org/10.1016/0022-0728(87)80135-3.

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42

Rao, K. Sreenivasa, M. M. Palrecha, and R. G. Dhaneshwar. "Determination of trace vanadium in various waters by differential pulse adsorptive stripping voltammetry." Electroanalysis 9, no. 10 (1997): 804–6. http://dx.doi.org/10.1002/elan.1140091015.

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43

Radi, Abd-Elgawad, and Hassan El-samboskany. "Anodic Adsorptive Stripping Voltammetric Determination of Rafoxanide on Glassy Carbon Electrode." Combinatorial Chemistry & High Throughput Screening 23, no. 10 (2020): 1002–9. http://dx.doi.org/10.2174/1386207323666200422083339.

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Background: Rafoxanide (RFX) is an active agent against Fasciola hepatica, but it is prohibited for treatment of dairy animals whose milk is provided for human consumption. Objective: A reliable, fast, and simple method needs to be developed to monitor RFX residues in milk samples before distribution to consumers. Methods: In this work, the electrochemical oxidation of RFX was studied at glassy carbon electrodes (GCE) in Britton-Robinson buffer (BR) solutions over the pH range 2.0-12.0 using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The oxidation of the drug was accompl

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44

Hájková, Andrea, Vlastimil Vyskočil, Aleš Daňhel, Joseph Wang, and Jiří Barek. "Polarographic and voltammetric determination of genotoxic 2-aminofluoren-9-one at mercury electrodes." Collection of Czechoslovak Chemical Communications 76, no. 12 (2011): 1775–90. http://dx.doi.org/10.1135/cccc2011142.

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Electrochemical behavior of genotoxic 2-aminofluoren-9-one (2-AFN) was investigated by DC tast polarography (DCTP) and differential pulse polarography (DPP), both at a classical dropping mercury electrode (DME), and by DC voltammetry (DCV), differential pulse voltammetry (DPV), and adsorptive stripping differential pulse voltammetry (AdSDPV), all at a miniaturized hanging mercury drop minielectrode (HMDmE), in buffered aqueous-methanolic solutions. Optimum conditions were found for the determination of 2-AFN by DCTP at DME in the concentration range from 1 × 10–6to 1 × 10–4mol l–1(with a limit

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45

Eskiköy, Dilek, Zehra Durmuş, and Esma Kiliç. "Electrochemical oxidation of atorvastatin and its adsorptive stripping determination in pharmaceutical dosage forms and biological fluids." Collection of Czechoslovak Chemical Communications 76, no. 12 (2011): 1633–49. http://dx.doi.org/10.1135/cccc2011117.

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Electrochemical behavior of atorvastatin (AT) and optimum conditions to its quantitative determination were investigated using voltammetric methods. Some electrochemical parameters such as diffusion coefficient, surface coverage of adsorbed molecules, electron transfer coefficient, standard rate constant and number of electrons were calculated using the results of cyclic voltammetry. A tentative mechanism for the oxidation for AT has been suggested. The oxidation signal of AT molecule was used to develop fully validated, new, rapid, selective and simple square-wave anodic adsorptive stripping

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46

Liu, Benzhi, and Min Wang. "Selective Determination of Iron(III) in Sea Water by Gold Nanoparticles Self-assembled with N-carboxyl- L-cysteine." Journal of New Materials for Electrochemical Systems 17, no. 1 (2014): 001–4. http://dx.doi.org/10.14447/jnmes.v17i1.274.

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Application of gold nanoparticles self-assembled with N-carboxyl- L-cysteine for the determination of iron(III) was investigated. Differential pulse adsorptive stripping voltammetry was used to detect iron(III). Various operational parameters were investigated and discussed in terms of their effects on the measurement signals. A linear range from 0.1 nM to 1.8 nM with a detection limit of 0.03 nMwas obtained under optimized conditions. The applicability of the method was successfully tested by determination of iron(III) in sea water samples.

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47

Ahmadi, Farhad, Sahar Ghasemi, and Mehdi Rahimi-Nasrabadi. "Adsorptive cathodic stripping determination of minoxidil in pharmaceutical, cream and shampoo products." Collection of Czechoslovak Chemical Communications 76, no. 5 (2011): 371–82. http://dx.doi.org/10.1135/cccc2011001.

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The cyclic voltammetric behavior of minoxidil was studied in a buffer with pH 3. Contradictory to that mentioned in a previously published work, the cyclic voltammogram of minoxidil exhibited a single 2-electron irreversible reduction wave in a buffer with pH 3. This wave was attributed to the reduction of the N→O bond. The cathodic differential pulse wave height decreased on the increase of pH till it disappeared in solution with pH 7.2. The quantitative trace determination of minoxidil was studied at a hanging mercury drop electrode by adsorptive cathodic stripping voltammetry. A fully valid

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48

Nida, Aydoğdu, Demir Ersin, SARIKURKCU Cengiz, and Burak ACIKGUL M. "Developing and Analytical Application of Modified Electrode for the Electrochemical Determination of RFX Veterinary Drug." International Bulletin of Electrochemical Methodology 2022, no. 1 (2022): 1–11. https://doi.org/10.2022/INTBECM.7413294.

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Rafoxanide (RFX) drug substance, belongs to the salicylanilide group of anthelmintic drugs. In this work, Electrochemical behaviour and analytical applications of RFX were investigated by the cyclic voltammetry (CV), adsorptive stripping square-wave voltammetry (AdSSWV), and adsorptive stripping differential pulse voltammetry (AdSDPV) on modified titanium dioxide/multi-walled carbon paste electrode (TiO<sub>2</sub>/MWCNTPE). The RFX showed a well-defined anodic signal, and has an irreversible electrode reaction, at approximately 0.45 V in the optimum pH 6.0 Britton Robinson (BR) buffer solutio

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49

Macikova, Pavla, Vladimir Halouzka, Jan Hrbac, Petr Bartak, and Jana Skopalova. "Electrochemical Behavior and Determination of Rutin on Modified Carbon Paste Electrodes." Scientific World Journal 2012 (2012): 1–9. http://dx.doi.org/10.1100/2012/394756.

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The performances of ionic liquid (1-hexyl-3-methylimidazolium-bis(trifluoromethylsulfonyl)imide, IL/CPE) and iron phthalocyanine (IP/CPE) modified carbon paste electrodes in electroanalytical determinations of rutin were evaluated and compared to the performance of unmodified carbon paste electrode (CPE). Cyclic voltammetry (CV), differential pulse voltammetry (DPV), differential pulse adsorptive stripping voltammetry (DPAdSV), and amperometry were used for rutin analysis. The best current responses of rutin were obtained at pH 4.0 for all tested techniques. IL/CPE electrode was found to perfo

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Kočmíd, Václav, Miroslav Podolák, Jiří Čoupek, and Oskar Andrýsek. "Possibility of determination of some derivatives of pterin important in the diagnostics of malignant tumours by using differential pulse polarography." Collection of Czechoslovak Chemical Communications 51, no. 1 (1986): 34–44. http://dx.doi.org/10.1135/cccc19860034.

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The polarographic behaviour of 6,7-dimethylpterin, xanthopterin, 6-pterinaldehyde, neopterin and 6-hydroxymethylpterin was investigated. These compounds are suitably determined by employing differential pulse polarography; some results suggest the possibility of their determination by cathodic stripping voltammetry with adsorptive accumulation. For all compounds, the effect of pH on polarographic reduction was examined. Under optimal conditions, the calibration curve of all compounds under investigation was linear in the range 2 . 10-6 - 1 . 10-7 mol/l and the detection limit was below 1 . 10-

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