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Journal articles on the topic 'Anodic stripping voltammtry'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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1

Bertazzoli, R., M. Ballester Santos, and E. Bresciani. "Tinplate anodic stripping voltammetry." Electrochimica Acta 36, no. 9 (January 1991): 1501–3. http://dx.doi.org/10.1016/0013-4686(91)85340-d.

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2

Fernando, Angelo Ransirimal, and Byron Kratochvil. "Internal standards in differential pulse anodic stripping voltammetry." Canadian Journal of Chemistry 69, no. 4 (April 1, 1991): 755–58. http://dx.doi.org/10.1139/v91-111.

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The use of lead and cadmium as internal standards for each other in anodic stripping analysis was investigated. Although accuracy was not affected, precision was significantly improved. The surface active agents Triton-X 100 and starch affected the sensitivity of the anodic stripping procedure for lead and cadmium, leading to error if a calibration curve is used. Data for application of the procedure to the analysis of the marine biological reference material LUTS-1 and soil reference materials SO-2, SO-3, and SO-4 are provided. Key words: internal standard, anodic stripping voltammetry, calibration curve, standard addition, lead determination, cadmium determination.

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3

Mazerie, Isabelle, and Florence Geneste. "Coupling of Anodic Stripping Voltammetry with Sampled-Current Voltammetry on an Electrode Array: Application to Lead Detection." Sensors 20, no. 5 (February 29, 2020): 1327. http://dx.doi.org/10.3390/s20051327.

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Electrochemical detection systems are very promising for pollution monitoring owing to their easy miniaturization and low cost. For this purpose, we have recently developed a new concept of device based on Electrodes Array for Sampled-Current Voltammetry (EASCV), which is compatible with miniaturization and portability. In this work, to improve the sensitivity of the analytical method, we added a preconcentration step before EASCV analysis, combining sampled-current voltammetry with anodic stripping voltammetry. Lead was chosen as analyte for this probe of concept owing to its high toxicity. The conditions for electrodeposition of lead on gold were optimized by means of under potential deposition. Current intensities 300 times higher than with linear sweep anodic stripping voltammetry were obtained, showing the interest in the method. The value of the sampling time directly affected the sensitivity of the sensor given by the slope of the linear calibration curve. The sensor exhibited a limit of detection of 1.16 mg L−1, similar to those obtained with linear sweep anodic stripping voltammetry.

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4

Vicentebeckett, VA. "The Underpotential Adsorption/Deposition and Stripping of Mercury on Gold in Dilute Sulfuric Acid." Australian Journal of Chemistry 42, no. 12 (1989): 2107. http://dx.doi.org/10.1071/ch9892107.

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The underpotential deposition of mercury on gold was studied by potentiostatic techniques at a rotating gold ring-disc electrode. Underpotential mercury deposition occurred at potentials more positive than 680 mV (against a dynamic hydrogen electrode). Anodic stripping voltammetry at the disc with ring collection showed that a monolayer coverage of underpotential mercury was equivalent to approximately 370pc/cm2. The stripping process yielded several anodic peaks and produced largely HgII, at least 16% of which remained adsorbed on the bare gold electrode. Potential-step experiments at the disc and ring-shielding data indicated that the underpotential shift was about 500 mV and that the deposition process involved both adsorbed (35-47% of the theoretical monolayer coverage) and soluble mercury(II) species. The adsorbed mercury had a formal positive charge of 0.40-0.46. The most anodic stripping peak (at 1200 mV) of underpotential mercury may be used to determine nanomolar levels of mercury by anodic stripping voltammetry, by using an overvoltage of less than 100 mV for preelectrolysis.

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5

Irdhawati, Irdhawati, Liana Sari, and Ida Ayu Raka Astiti Asih. "TEKNIK VOLTAMETRI PELUCUTAN ANODIK GELOMBANG PERSEGI UNTUK PENENTUAN KADAR LOGAM Cu DALAM KANGKUNG AIR." Jurnal Kimia Riset 1, no. 2 (December 21, 2016): 122. http://dx.doi.org/10.20473/jkr.v1i2.3094.

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ABSTRAK Analisis logam berat Cu(II) dilakukan dengan metode voltametri pelucutan anodik gelombang persegi. Penelitian ini bertujuan untuk mengetahui validitas metode voltametri pelucutan anodik yang digunakan dalam pengukuran kadar logam Cu(II) dalam sampel kangkung air di muara sungai Badung. Elektroda glassy carbon digunakan sebagai elektroda kerja, Ag/AgCl sebagai elektroda pembanding, dan kawat platina sebagai elektroda pembantu. Parameter yang dioptimasi meliputi waktu deposisi dan laju pindai dalam larutan standar Cu(II) 500 ppb. Validasi metode ditentukan dengan menentukan rentang konsentrasi linier, limit deteksi, keberulangan pengukuran, dan persen perolehan kembali. Teknik voltametri pelucutan anodik kemudian digunakan untuk mengukur kadar logam Cu(II) pada sampel kangkung air.Hasil optimasi pengukuran kadar logam Cu(II) yaitu waktu deposisi optimum 60 detik dan laju pindai optimum 10 mV/detik. Pengukuran validitas larutan standar logam Cu(II), rentang konsentrasi linier larutan 50 ~500 ppb dan memiliki nilai koefisien korelasi 0,9983. Limit deteksi 35 ppb, keberulangan pengukuran memiliki rasio Horwitz kurang dari 2, dan persen perolehan kembali 99,35% ± 0,4526. Hasil pengukuran sampel tanaman kangkung memiliki kandungan logam Cu(II) sebesar 4,0 ppm. Berdasarkan Keputusan Direktur Jenderal Pengawasan Obat dan Makanan batas maksimum cemaran logam dalam makanan untuk logam Cu(II) adalah 5,0 ppm. Oleh karena itu dapat diketahui bahwa kandungan logam Cu(II) tidak melebihi kadar maksimum yang diperkenankan. Kata Kunci : logam berat, voltametri pelucutan anodik gelombang persegi, kangkung airABSTRACTHeavy metal analysis of Cu(II) was measured by square wave anodic stripping voltammetry method. The aim of this research is to know the validity of square wave anodic stripping voltammetry method for determination of Cu(II) in water spinach from the estuary of Badung river. Glassy carbon, Ag/AgCl, and Pt wire electrodes were used as working electrode, reference electrode and counter electrode, respectively. Optimized parameter involved the deposition time and scan rate in standard solution Cu(II) 500 ppb. Furthermore, the validation method was examined by determination of linear concentration range, limit of detection, repetition of measurement, and percent of recovery. Moreover, the result of validation was used for observing of heavy metal Cu(II) content in water spinach. The result of optimum deposition time is 60 s. Meanwhile, the scan rate optimum is 10 mV/s. Measurement for standard solution 50 ~ 500 ppb on linear concentration range, with correlation coefficient 0,9983. Limit of detection is 35 ppb, repetition of measurement for metal has Horwitz ratio less than 2, and percent recovery of Cu(II) measurement is 99,35% ± 0,4526. The measurement of Cu(II) content in the water spinach sample contain Cu(II) 4,0 ppm. Based on Decree of Directorate General for Drug and Food Control, the treshold line for Cu(II) contamination for food is 5,0 ppm. Therefore, the water spinach sample contain Cu(II) is less than accepted value. Keyword : Heavy metal, square wave anodic stripping voltammetry, water spinach

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6

Navrátil, Tomáš, Jiří Barek, and Miloslav Kopanica. "Anodic stripping voltammetry using graphite composite solid electrode." Collection of Czechoslovak Chemical Communications 74, no. 11-12 (2009): 1807–26. http://dx.doi.org/10.1135/cccc2009107.

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A graphite (carbon) composite solid electrode, prepared from graphite powder and epoxy resin, was used as a working electrode for anodic stripping voltammetry. The underpotential deposition effect, which appears at metallic electrodes, was clearly observed on this type of electrode as well. In the case of a simultaneous deposition of two metals on the surface of the composite solid electrode, the anodic dissolution of the metal, which is anodically dissolved at more negative potentials, is substantially influenced by the presence of the other deposited metal. This effect was exploited for the determination of lead in the presence of other metals by differential pulse anodic stripping voltammetry. The article presents possible applicability of such a type of very simple composite electrode to studies of the underpotential deposition effect as well as for analytical purposes.

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7

Bezerra dos Santos, Vagner, Elson Luiz Fava, Osmundo Dantas Pessoa-Neto, Silmara Rossana Bianchi, Ronaldo Censi Faria, and Orlando Fatibello-Filho. "A versatile and robust electrochemical flow cell with a boron-doped diamond electrode for simultaneous determination of Zn2+ and Pb2+ ions in water samples." Anal. Methods 6, no. 21 (2014): 8526–34. http://dx.doi.org/10.1039/c4ay01811g.

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8

Xue, Huifeng, Jinwen Zheng, Qiaoyun Chen, Qingshui Wang, Yao Lin, and Jianchui Chen. "Ag+-coordinated oligonucleotides on gold nanoparticles for anodic-stripping voltammetric immunoassay of cancer antigen 125 for cervical carcinoma." Analytical Methods 11, no. 23 (2019): 2976–82. http://dx.doi.org/10.1039/c9ay00875f.

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9

Motkosky, Norine, Angelo Ransirimal Fernando, and Byron Kratochvil. "Elemental analysis of the marine biological reference material LUTS-1 by instrumental neutron activation, graphite furnace atomic absorption spectroscopy, and anodic stripping voltammetry." Canadian Journal of Chemistry 68, no. 5 (May 1, 1990): 735–40. http://dx.doi.org/10.1139/v90-116.

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Marine biological reference material LUTS-1, lobster heptopancreas, was analyzed for elemental homogeneity using graphite furnace atomic absorption, anodic stripping voltammetry, and neutron activation analysis. Analysis of samples taken from 12 bottles of LUTS-1 bottled on two different days showed no statistical differences at the 95% confidence level for within-bottle variance for a large number of elements. Differences were observed for between-day variances for aluminum, iron, cobalt, sodium, chlorine, bromine, and iodine, but not at a level sufficient to affect utility as a reference material. Keywords: neutron activation analysis, graphite furnace atomic absorportion spectroscopy, anodic stripping voltammetry, elemental analysis, marine biological reference material.

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10

Ustinova, Elvira M., Eduard Gorchakov, and Alina V. Melkova. "Monitoring the Palladium Contents in the Tailings Using Stripping Voltammetry." Key Engineering Materials 712 (September 2016): 328–31. http://dx.doi.org/10.4028/www.scientific.net/kem.712.328.

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Anodic stripping voltammetry, a classical electroanalytical method has been optimized to analyze trace Pd (II) in tailings. The authors identified the registration conditions in the determination of the analytical signal Pd (II): the composition of background electrolyte and the electrolysis potential. The electroanalytical approaches with an unmodified carbon electrode were used. The use of stripping voltammetry applied to the assessment of the palladium content in geological objects was demonstrated.

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11

Bu, Lijuan, Qingji Xie, and Hai Ming. "Simultaneous sensitive analysis of Cd(ii), Pb(ii) and As(iii) using a dual-channel anodic stripping voltammetry approach." New Journal of Chemistry 44, no. 15 (2020): 5739–45. http://dx.doi.org/10.1039/d0nj00545b.

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12

Wehmeyer, Kenneth R., and R. Mark Wightman. "Cyclic voltammetry and anodic stripping voltammetry with mercury ultramicroelectrodes." Analytical Chemistry 57, no. 9 (August 1985): 1989–93. http://dx.doi.org/10.1021/ac00286a046.

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13

Jaiswal, A. K., Srinita Das, Vinod Kumar, Madhuri Gupta, and N. Singh. "Simultaneous Determination of Zinc (Zn), Cadmium (Cd), Lead (Pb) and Copper (Cu) in Blood Using Differential- Pulse Anodic-Stripping Voltammetry." International Journal of Engineering Research 4, no. 5 (May 1, 2015): 235–39. http://dx.doi.org/10.17950/ijer/v4s5/505.

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14

Luong, John H. T., Edmond Lam, and Keith B. Male. "Recent advances in electrochemical detection of arsenic in drinking and ground waters." Anal. Methods 6, no. 16 (2014): 6157–69. http://dx.doi.org/10.1039/c4ay00817k.

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Anodic stripping voltammetry (ASV) using noble electrodes is based on the reduction of As³⁺ to As⁰, followed by its stripping or oxidation to As³⁺ or As⁵⁺ species, the two predominant forms of arsenic in water.

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15

Kowalik, R. "The Voltammetric Analysis of Selenium Electrodeposition from H2SeO3 Solution on Gold Electrode." Archives of Metallurgy and Materials 60, no. 1 (April 1, 2015): 57–63. http://dx.doi.org/10.1515/amm-2015-0009.

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Abstract 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.

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16

Borrill, Alexandra J., Nicole E. Reily, and Julie V. Macpherson. "Addressing the practicalities of anodic stripping voltammetry for heavy metal detection: a tutorial review." Analyst 144, no. 23 (2019): 6834–49. http://dx.doi.org/10.1039/c9an01437c.

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17

Sahoo, S., A. K. Satpati, and A. V. R. Reddy. "Electrodeposited Bi-Au nanocomposite modified carbon paste electrode for the simultaneous determination of copper and mercury." RSC Advances 5, no. 33 (2015): 25794–800. http://dx.doi.org/10.1039/c5ra02977e.

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18

Jiang, Chuanjia, and Heileen Hsu-Kim. "Direct in situ measurement of dissolved zinc in the presence of zinc oxide nanoparticles using anodic stripping voltammetry." Environ. Sci.: Processes Impacts 16, no. 11 (2014): 2536–44. http://dx.doi.org/10.1039/c4em00278d.

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19

Peña, Roselyn C., Lorena Cornejo, Mauro Bertotti, and Christopher M. A. Brett. "Electrochemical determination of Cd(ii) and Pb(ii) in mining effluents using a bismuth-coated carbon fiber microelectrode." Analytical Methods 10, no. 29 (2018): 3624–30. http://dx.doi.org/10.1039/c8ay00949j.

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20

Wechter, Carolyn, Neal Sleszynski, John J. O'Dea, and Jane Osteryoung. "Anodic stripping voltammetry with flow injection analysis." Analytica Chimica Acta 175 (1985): 45–53. http://dx.doi.org/10.1016/s0003-2670(00)82716-6.

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21

Clark, Emily A., and Ingrid Fritsch. "Anodic Stripping Voltammetry Enhancement by Redox Magnetohydrodynamics." Analytical Chemistry 76, no. 8 (April 2004): 2415–18. http://dx.doi.org/10.1021/ac0354490.

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22

Florence, T. Mark. "Trace element speciation by anodic stripping voltammetry." Analyst 117, no. 3 (1992): 551. http://dx.doi.org/10.1039/an9921700551.

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23

Wang, Joseph. "Anodic stripping voltammetry as an analytical tool." Environmental Science & Technology 29, no. 2 (February 1995): 104A—109A. http://dx.doi.org/10.1021/es00002a724.

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24

Chapman, Conrad S, and Constant M G. van den Berg. "Anodic Stripping Voltammetry Using a Vibrating Electrode." Electroanalysis 19, no. 13 (July 2007): 1347–55. http://dx.doi.org/10.1002/elan.200703873.

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25

Deaver, Emily, and John H. Rodgers. "Measuring bioavailable copper using anodic stripping voltammetry." Environmental Toxicology and Chemistry 15, no. 11 (November 1996): 1925–30. http://dx.doi.org/10.1002/etc.5620151110.

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26

Clark, Emily A. "Anodic Stripping Voltammetry Enhancement by Redox Magnetohydrodynamics." Electrochemical Society Interface 12, no. 4 (December 1, 2003): 67–68. http://dx.doi.org/10.1149/2.f12034if.

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27

Hashemi, Farzaneh, Ali Reza Zanganeh, Farid Naeimi, and Maryam Tayebani. "Fabrication of an electrochemical sensor based on metal–organic framework ZIF-8 for quantitation of silver ions: optimizing experimental conditions using central composite design (CCD)." Analytical Methods 12, no. 23 (2020): 3045–55. http://dx.doi.org/10.1039/d0ay00843e.

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ZIF-8 was synthesized and carbon paste electrodes (CPEs) modified with this metal–organic framework were utilized for quantitation of silver(i) by the differential pulse anodic stripping voltammetry (DPASV) technique.

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28

Wang, Yangjuan, Yuanping Peng, Yifu Chen, Kejing Du, Yijun Li, and Xiwen He. "Sensitive determination of lead by differential pulse anodic stripping voltammetry on silver-based coordination complex modified electrodes." Analytical Methods 8, no. 8 (2016): 1935–41. http://dx.doi.org/10.1039/c5ay03148f.

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A silver-based coordination complex was synthesized from melamine (MA), terephthalic acid (TPA) and silver nitrate for the determination of Pb²⁺ at the trace level by differential pulse anodic stripping voltammetry (DPASV).

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29

Stojanović, Zorica, Zuzana Koudelkova, Eliska Sedlackova, David Hynek, Lukas Richtera, and Vojtech Adam. "Determination of chromium(vi) by anodic stripping voltammetry using a silver-plated glassy carbon electrode." Analytical Methods 10, no. 24 (2018): 2917–23. http://dx.doi.org/10.1039/c8ay01047a.

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In this work, differential pulse anodic stripping voltammetry (DP-ASV) for the determination of trace amounts of hexavalent chromium (Cr(vi)) at a silver plated glassy carbon electrode (Ag plated-GCE) is described in detail.

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30

Gonzalez, Camila, Olimpo García-Beltrán, and Edgar Nagles. "A new and simple electroanalytical method to detect thiomersal in vaccines on a screen-printed electrode modified with chitosan." Analytical Methods 10, no. 10 (2018): 1196–202. http://dx.doi.org/10.1039/c8ay00161h.

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The use of a screen-printed electrode modified with chitosan (Cs) to determine thiomersal (TMS) through the oxidation of thiosalicylic acid by linear sweep anodic stripping voltammetry is reported for the first time in this work.

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31

Wang, Haofan, Yin Guo, and Hongcheng Pan. "Determination of selenium and copper in water and food by hierarchical dendritic nano-gold modified glassy carbon electrodes." Analyst 146, no. 13 (2021): 4384–90. http://dx.doi.org/10.1039/d1an00658d.

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Hierarchical dendritic gold nanostructured films were electrodeposited on a GCE at a potential of −0.6 V and used for square-wave anodic stripping voltammetry to determine nanomolar levels of Se and Cu in water and food.

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32

Li, Chao, Xiaole Zhao, and Xiaojun Han. "Simultaneous determination of trace Cd2+ and Pb2+ using GR/l-cysteine/Bi modified screen-printed electrodes." Analytical Methods 10, no. 40 (2018): 4945–50. http://dx.doi.org/10.1039/c8ay01676c.

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A GR/l-cys/Bi/SPE (reduced graphene oxide/l-cysteine/Bi/screen-printed electrode) was prepared to simultaneously determine Cd²⁺ and Pb²⁺ ions by using SWASV (square wave anodic stripping voltammetry).

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33

Wang, Yangjuan, Kejing Du, Yifu Chen, Yijun Li, and Xiwen He. "Electrochemical determination of lead based on metal–organic framework MIL-101(Cr) by differential pulse anodic stripping voltammetry." Analytical Methods 8, no. 15 (2016): 3263–69. http://dx.doi.org/10.1039/c6ay00183a.

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Green octahedral crystals of MIL-101(Cr) were synthesized and used for the determination of Pb²⁺ at the trace level by differential pulse anodic stripping voltammetry (DPASV) because of their good adsorption capability for Pb²⁺.

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34

Cao, Qiang, Yushi Xiao, Rong Huang, Na Liu, Hai Chi, Cheng-Te Lin, Chi-Hsien Huang, Gang Han, and Lidong Wu. "Thiolated poly(aspartic acid)-functionalized two-dimensional MoS2, chitosan and bismuth film as a sensor platform for cadmium ion detection." RSC Advances 10, no. 62 (2020): 37989–94. http://dx.doi.org/10.1039/d0ra06197b.

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In this work, a sensitive electrochemical platform for determination of cadmium ions (Cd²⁺) is obtained using thiolated poly(aspartic acid) (TPA)-functionalized MoS₂ as a sensor platform by differential pulse anodic stripping voltammetry (DPASV).

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35

Cloake, Samantha J., Her Shuang Toh, Patricia T. Lee, Chris Salter, Colin Johnston, and Richard G. Compton. "Anodic Stripping Voltammetry of Silver Nanoparticles: Aggregation Leads to Incomplete Stripping." ChemistryOpen 4, no. 1 (October 13, 2014): 22–26. http://dx.doi.org/10.1002/open.201402050.

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36

Silva, Iasmin B., Danyelle Medeiros de Araújo, Marco Vocciante, Sergio Ferro, Carlos A. Martínez-Huitle, and Elisama V. Dos Santos. "Electrochemical Determination of Lead Using A Composite Sensor Obtained from Low-Cost Green Materials:Graphite/Cork." Applied Sciences 11, no. 5 (March 6, 2021): 2355. http://dx.doi.org/10.3390/app11052355.

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The purpose of this study was to develop an inexpensive, simple, and highly selective cork-modified carbon paste electrode for the determination of Pb(II) by differential pulse anodic stripping voltammetry (DPASV) and square-wave anodic stripping voltammetry (SWASV). Among the cork–graphite electrodes investigated, the one containing 70% w/w carbon showed the highest sensitivity for the determination of Pb(II) in aqueous solutions. Under SWASV conditions, its linear range and relative standard deviation are equal to 1–25 µM and 1.4%, respectively; the limit of detection complies with the value recommended by the World Health Organization. To optimize the operating conditions, the selectivity and accuracy of the analysis were further investigated by SWASV in acidic media. Finally, the electrode was successfully applied for the determination of Pb(II) in natural water samples, proving to be a sensitive electrochemical sensor that meets the stringent environmental control requirements.

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37

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 mol l–1 for anodic differential pulse voltammetry in a mixture of Britton–Robinson buffer (pH 11)–methanol 1:1 (v/v) and 1.6 × 10–7 mol l–1 for HPLC with electrochemical detection (E = +1.2 V) in a mobile phase Britton–Robinson buffer (pH 7)–methanol 1:9 (v/v).

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38

Lintern, Melvyn, Alan Mann, and Dale Longman. "The determination of gold by anodic stripping voltammetry." Analytica Chimica Acta 209 (1988): 193–203. http://dx.doi.org/10.1016/s0003-2670(00)84562-6.

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39

Jasinski, M., A. Kirbs, M. Schmehl, and P. Gründler. "Heated mercury film electrode for anodic stripping voltammetry." Electrochemistry Communications 1, no. 1 (January 1999): 26–28. http://dx.doi.org/10.1016/s1388-2481(98)00008-3.

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40

Wang, Joseph, Jianmin Lu, Samo B. Hocevar, Percio A. M. Farias, and Bozidar Ogorevc. "Bismuth-Coated Carbon Electrodes for Anodic Stripping Voltammetry." Analytical Chemistry 72, no. 14 (July 2000): 3218–22. http://dx.doi.org/10.1021/ac000108x.

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41

Tay, Eddie Boon-Tat, Soo-Beng Khoo, and Siau-Gek Ang. "Oxygen removal in flow injection anodic stripping voltammetry." Analyst 114, no. 10 (1989): 1271. http://dx.doi.org/10.1039/an9891401271.

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42

Guanghan, Lu, Jin Hong, and Song Dandan. "Determination of trace nitrite by anodic stripping voltammetry." Food Chemistry 59, no. 4 (August 1997): 583–87. http://dx.doi.org/10.1016/s0308-8146(96)00290-7.

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43

Vandaveer and Ingrid Fritsch. "Measurement of Ultrasmall Volumes Using Anodic Stripping Voltammetry." Analytical Chemistry 74, no. 14 (July 2002): 3575–78. http://dx.doi.org/10.1021/ac011036s.

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44

Caruana, Daren J., and Joseph Giglio. "Electrochemical detection of halothane by anodic stripping voltammetry." Journal of the Chemical Society, Faraday Transactions 92, no. 19 (1996): 3669. http://dx.doi.org/10.1039/ft9969203669.

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45

Zlatev, Roumen K., Margarita S. Stoytcheva, Benjamin S. Valdez, Jean-Pierre Magnin, and Zdravka Velkova. "Anodic Stripping Differential Alternative Pulses Voltammetry and Applications." ECS Transactions 13, no. 15 (December 18, 2019): 57–63. http://dx.doi.org/10.1149/1.3002808.

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46

Félix, Luis Tomás, Sergio Miguel Durón, Verónica Ávila, Hans Christian Correa, and Miguel Mauricio Aguilera. "Determination of Pb inBrickellia Veronicifoliafor Anodic Stripping Voltammetry." ECS Transactions 84, no. 1 (January 31, 2018): 297–304. http://dx.doi.org/10.1149/08401.0297ecst.

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Surmann, Peter, and Hanan Channaa. "Anodic Stripping Voltammetry with Galinstan as Working Electrode." Electroanalysis 27, no. 7 (April 29, 2015): 1726–32. http://dx.doi.org/10.1002/elan.201400752.

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Hull, Ewa, Robert Piech, and Władysław W Kubiak. "Iridium Oxide Film Electrodes for Anodic Stripping Voltammetry." Electroanalysis 20, no. 19 (October 2008): 2070–75. http://dx.doi.org/10.1002/elan.200804295.

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Omanović, D., Ž. Peharec, T. Magjer, M. Lovrić, and M. Branica. "Wall-Jet electrode system for anodic stripping voltammetry." Electroanalysis 6, no. 11-12 (November 1994): 1029–33. http://dx.doi.org/10.1002/elan.1140061119.

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Malakhova, Natalia A., Galina N. Popkova, Gertrud Wittmann, Liubov N. Kalnichevskaia, and Khjena Z. Brainina. "Anodic stripping voltammetry of tungsten at graphite electrodes." Electroanalysis 8, no. 4 (April 1996): 375–80. http://dx.doi.org/10.1002/elan.1140080414.

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