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Search results for: electrochemical performance

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class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Commenced</strong> in January 2007</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Frequency:</strong> Monthly</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Edition:</strong> International</div> </div> </div> <div class="col-sm-3"> <div class="card"> <div class="card-body"><strong>Paper Count:</strong> 13585</div> </div> </div> </div> <h1 class="mt-3 mb-3 text-center" style="font-size:1.6rem;">Search results for: electrochemical performance</h1> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13525</span> Fast Prototyping of Precise, Flexible, Multiplexed, Printed Electrochemical Enzyme-Linked Immunosorbent Assay Platform for Point-of-Care Biomarker Quantification</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zahrasadat%20Hosseini">Zahrasadat Hosseini</a>, <a href="https://publications.waset.org/abstracts/search?q=Jie%20Yuan"> Jie Yuan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Point-of-care (POC) diagnostic devices based on lab-on-a-chip (LOC) technology have the potential to revolutionize medical diagnostics. However, the development of an ideal microfluidic system based on LOC technology for diagnostics purposes requires overcoming several obstacles, such as improving sensitivity, selectivity, portability, cost-effectiveness, and prototyping methods. While numerous studies have introduced technologies and systems that advance these criteria, existing systems still have limitations. Electrochemical enzyme-linked immunosorbent assay (e-ELISA) in a LOC device offers numerous advantages, including enhanced sensitivity, decreased turnaround time, minimized sample and analyte consumption, reduced cost, disposability, and suitability for miniaturization, integration, and multiplexing. In this study, we present a novel design and fabrication method for a microfluidic diagnostic platform that integrates screen-printed electrochemical carbon/silver chloride electrodes on flexible printed circuit boards with flexible, multilayer, polydimethylsiloxane (PDMS) microfluidic networks to accurately manipulate and pre-immobilize analytes for performing electrochemical enzyme-linked immunosorbent assay (e-ELISA) for multiplexed quantification of blood serum biomarkers. We further demonstrate fast, cost-effective prototyping, as well as accurate and reliable detection performance of this device for quantification of interleukin-6-spiked samples through electrochemical analytics methods. We anticipate that our invention represents a significant step towards the development of user-friendly, portable, medical-grade POC diagnostic devices. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=lab-on-a-chip" title="lab-on-a-chip">lab-on-a-chip</a>, <a href="https://publications.waset.org/abstracts/search?q=point-of-care%20diagnostics" title=" point-of-care diagnostics"> point-of-care diagnostics</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20ELISA" title=" electrochemical ELISA"> electrochemical ELISA</a>, <a href="https://publications.waset.org/abstracts/search?q=biomarker%20quantification" title=" biomarker quantification"> biomarker quantification</a>, <a href="https://publications.waset.org/abstracts/search?q=fast%20prototyping" title=" fast prototyping"> fast prototyping</a> </p> <a href="https://publications.waset.org/abstracts/169508/fast-prototyping-of-precise-flexible-multiplexed-printed-electrochemical-enzyme-linked-immunosorbent-assay-platform-for-point-of-care-biomarker-quantification" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/169508.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">93</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13524</span> Photo-Electrochemical/Electro-Fenton Coupling Oxidation System with Fe/Co-Based Anode and Cathode Metal-Organic Frameworks Derivative Materials for Sulfamethoxazole Treatment</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Xin%20Chen">Xin Chen</a>, <a href="https://publications.waset.org/abstracts/search?q=Xinyong%20Li"> Xinyong Li</a>, <a href="https://publications.waset.org/abstracts/search?q=Qidong%20Zhao"> Qidong Zhao</a>, <a href="https://publications.waset.org/abstracts/search?q=Dong%20Wang"> Dong Wang</a> </p> <p class="card-text"><strong>Abstract:</strong></p> A new coupling system was constructed by combining photo-electrochemical cell with electro-fenton cell (PEC-EF). The electrode material in this system was derived from MnyFe₁₋yCo Prussian-Blue-Analog (PBA). Mn₀.₄Fe₀.₆Co₀.₆₇-N@C spin-coated on carbon paper behaved as the gas diffusion cathode and Mn₀.₄Fe₀.₆Co₀.₆₇O₂.₂ spin-coated on fluorine-tin oxide glass (FTO) as anode. The two separated cells could degrade Sulfamethoxazole (SMX) simultaneously and some coupling mechanisms by PEC and EF enhancing the degradation efficiency were investigated. The continuous on-site generation of H₂O₂ at cathode through an oxygen reduction reaction (ORR) was realized over rotating ring-disk electrode (RRDE). The electron transfer number (n) of the ORR with Mn₀.₄Fe₀.₆Co₀.₆₇-N@C was 2.5 in the selected potential and pH range. The photo-electrochemical properties of Mn₀.₄Fe₀.₆Co₀.₆₇O₂.₂ were systematically studied, which displayed good response towards visible light. The photoinduced electrons at anode can transfer to cathode for further use. Efficient photo-electro-catalytic performance was observed in degrading SMX. Almost 100% SMX removal was achieved in 120 min. This work not only provided a highly effective technique for antibiotic treatment but also revealed the synergic effect between PEC and EF. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=electro-fenton" title="electro-fenton">electro-fenton</a>, <a href="https://publications.waset.org/abstracts/search?q=photo-electrochemical" title=" photo-electrochemical"> photo-electrochemical</a>, <a href="https://publications.waset.org/abstracts/search?q=synergic%20effect" title=" synergic effect"> synergic effect</a>, <a href="https://publications.waset.org/abstracts/search?q=sulfamethoxazole" title=" sulfamethoxazole"> sulfamethoxazole</a> </p> <a href="https://publications.waset.org/abstracts/83517/photo-electrochemicalelectro-fenton-coupling-oxidation-system-with-feco-based-anode-and-cathode-metal-organic-frameworks-derivative-materials-for-sulfamethoxazole-treatment" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/83517.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">184</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13523</span> Application of Electrochemical Impedance Spectroscopy to Monitor the Steel/Soil Interface During Cathodic Protection of Steel in Simulated Soil Solution</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mandlenkosi%20George%20Robert%20Mahlobo">Mandlenkosi George Robert Mahlobo</a>, <a href="https://publications.waset.org/abstracts/search?q=Tumelo%20Seadira"> Tumelo Seadira</a>, <a href="https://publications.waset.org/abstracts/search?q=Major%20Melusi%20Mabuza"> Major Melusi Mabuza</a>, <a href="https://publications.waset.org/abstracts/search?q=Peter%20Apata%20Olubambi"> Peter Apata Olubambi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Cathodic protection (CP) has been widely considered a suitable technique for mitigating corrosion of buried metal structures. Plenty of efforts have been made in developing techniques, in particular non-destructive techniques, for monitoring and quantifying the effectiveness of CP to ensure the sustainability and performance of buried steel structures. The aim of this study was to investigate the evolution of the electrochemical processes at the steel/soil interface during the application of CP on steel in simulated soil. Carbon steel was subjected to electrochemical tests with NS4 solution used as simulated soil conditions for 4 days before applying CP for a further 11 days. A previously modified non-destructive voltammetry technique was applied before and after the application of CP to measure the corrosion rate. Electrochemical impedance spectroscopy (EIS), in combination with mathematical modeling through equivalent electric circuits, was applied to determine the electrochemical behavior at the steel/soil interface. The measured corrosion rate was found to have decreased from 410 µm/yr to 8 µm/yr between days 5 and 14 because of the applied CP. Equivalent electrical circuits were successfully constructed and used to adequately model the EIS results. The modeling of the obtained EIS results revealed the formation of corrosion products via a mixed activation-diffusion mechanism during the first 4 days, while the activation mechanism prevailed in the presence of CP, resulting in a protective film. The x-ray diffraction analysis confirmed the presence of corrosion products and the predominant protective film corresponding to the calcareous deposit. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=carbon%20steel" title="carbon steel">carbon steel</a>, <a href="https://publications.waset.org/abstracts/search?q=cathodic%20protection" title=" cathodic protection"> cathodic protection</a>, <a href="https://publications.waset.org/abstracts/search?q=NS4%20solution" title=" NS4 solution"> NS4 solution</a>, <a href="https://publications.waset.org/abstracts/search?q=voltammetry" title=" voltammetry"> voltammetry</a>, <a href="https://publications.waset.org/abstracts/search?q=EIS" title=" EIS"> EIS</a> </p> <a href="https://publications.waset.org/abstracts/182962/application-of-electrochemical-impedance-spectroscopy-to-monitor-the-steelsoil-interface-during-cathodic-protection-of-steel-in-simulated-soil-solution" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/182962.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">71</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13522</span> Improving Carbon Fiber Structural Battery Performance with Polymer Interface</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Kathleen%20Moyer">Kathleen Moyer</a>, <a href="https://publications.waset.org/abstracts/search?q=Nora%20Ait%20Boucherbil"> Nora Ait Boucherbil</a>, <a href="https://publications.waset.org/abstracts/search?q=Murtaza%20Zohair"> Murtaza Zohair</a>, <a href="https://publications.waset.org/abstracts/search?q=Janna%20Eaves-Rathert"> Janna Eaves-Rathert</a>, <a href="https://publications.waset.org/abstracts/search?q=Cary%20Pint"> Cary Pint</a> </p> <p class="card-text"><strong>Abstract:</strong></p> This study demonstrates the significance of interface engineering in the field of structural energy by being the first case where the performance of the system with the structural battery is greater than the performance of the same system with a battery separate from the system. The benefits of improving the interface in the structural battery were tested by creating carbon fiber composite batteries (and independent graphite electrodes and lithium iron phosphate electrodes) with and without an improved interface. Mechanical data on the structural batteries were collected using tensile tests and electrochemical data was collected using scanning electron microscopy equipment. The full-cell lithium-ion structural batteries had capacity retention of over 80% exceeding 100 cycles with an average energy density of 52 W h kg−1 and a maximum energy density of 58 W h kg−1. Most scientific developments in the field of structural energy have been done with supercapacitors. Most scientific developments with structural batteries have been done where batteries are simply incorporated into the structural element. That method has limited advantages and can create mechanical disadvantages. This study aims to show that a large improvement in structure energy research can be made by improving the interface between the structural device and the battery. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=composite%20materials" title="composite materials">composite materials</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20performance" title=" electrochemical performance"> electrochemical performance</a>, <a href="https://publications.waset.org/abstracts/search?q=mechanical%20properties" title=" mechanical properties"> mechanical properties</a>, <a href="https://publications.waset.org/abstracts/search?q=polymer%20interface" title=" polymer interface"> polymer interface</a>, <a href="https://publications.waset.org/abstracts/search?q=structural%20batteries" title=" structural batteries"> structural batteries</a> </p> <a href="https://publications.waset.org/abstracts/153279/improving-carbon-fiber-structural-battery-performance-with-polymer-interface" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/153279.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">114</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13521</span> An Electrochemical DNA Biosensor Based on Oracet Blue as a Label for Detection of Helicobacter pylori </h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Saeedeh%20Hajihosseini">Saeedeh Hajihosseini</a>, <a href="https://publications.waset.org/abstracts/search?q=Zahra%20Aghili"> Zahra Aghili</a>, <a href="https://publications.waset.org/abstracts/search?q=Navid%20Nasirizadeh"> Navid Nasirizadeh</a> </p> <p class="card-text"><strong>Abstract:</strong></p> An innovative method of a DNA electrochemical biosensor based on Oracet Blue (OB) as an electroactive label and gold electrode (AuE) for detection of Helicobacter pylori, was offered. A single–stranded DNA probe with a thiol modification was covalently immobilized on the surface of the AuE by forming an Au–S bond. Differential pulse voltammetry (DPV) was used to monitor DNA hybridization by measuring the electrochemical signals of reduction of the OB binding to double– stranded DNA (ds–DNA). Our results showed that OB–based DNA biosensor has a decent potential for detection of single–base mismatch in target DNA. Selectivity of the proposed DNA biosensor was further confirmed in the presence of non–complementary and complementary DNA strands. Under optimum conditions, the electrochemical signal had a linear relationship with the concentration of the target DNA ranging from 0.3 nmol L-1 to 240.0 nmol L-1, and the detection limit was 0.17 nmol L-1, whit a promising reproducibility and repeatability. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=DNA%20biosensor" title="DNA biosensor">DNA biosensor</a>, <a href="https://publications.waset.org/abstracts/search?q=oracet%20blue" title=" oracet blue"> oracet blue</a>, <a href="https://publications.waset.org/abstracts/search?q=Helicobacter%20pylori" title=" Helicobacter pylori"> Helicobacter pylori</a>, <a href="https://publications.waset.org/abstracts/search?q=electrode%20%28AuE%29" title=" electrode (AuE)"> electrode (AuE)</a> </p> <a href="https://publications.waset.org/abstracts/53867/an-electrochemical-dna-biosensor-based-on-oracet-blue-as-a-label-for-detection-of-helicobacter-pylori" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/53867.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">271</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13520</span> An Electrode Material for Ultracapacitors: Hydrothermal Synthesis of Neodymium Oxide/Manganese Oxide/Nitrogen Doped Reduced Graphene Oxide Ternary Nanocomposites</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=K.%20Saravanan">K. Saravanan</a>, <a href="https://publications.waset.org/abstracts/search?q=K.%20A.Rameshkumar"> K. A.Rameshkumar</a>, <a href="https://publications.waset.org/abstracts/search?q=P.%20Maadeswaran"> P. Maadeswaran</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The depletion of fossil resources and the rise in global temperatures are two of the most important concerns we confront today. There are numerous renewable energy sources like solar power, tidal power, wind energy, radiant energy, hydroelectricity, geothermal energy, and biomass available to generate the needed energy demand. Engineers and scientists around the world are facing a massive barrier in the development of storage technologies for the energy developed from renewable energy sources. The development of electrochemical capacitors as a future energy storage technology is at the forefront of current research and development. This is due to the fact that the electrochemical capacitors have a significantly higher energy density, a faster charging-discharging rate, and a longer life span than capacitors, and they also have a higher power density than batteries, making them superior to both. In this research, electrochemical capacitors using the Nd2O3/Mn3O4/ N-rGO electrode material is chosen since the of hexagonal and tetragonal crystal structures of Nd2O3 and Mn3O4 and also has cycling stability of 68% over a long time at 50mVs-1 and a high coulombic efficiency of 99.64% at 5 Ag-1. This approach may also be used to create novel electrode materials with improved electrochemical and cyclic stability for high-performance supercapacitors. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Nd2O3%2FMn3O4%2FN-rGO" title="Nd2O3/Mn3O4/N-rGO">Nd2O3/Mn3O4/N-rGO</a>, <a href="https://publications.waset.org/abstracts/search?q=nanocomposites" title=" nanocomposites"> nanocomposites</a>, <a href="https://publications.waset.org/abstracts/search?q=hydrothermal%20method" title=" hydrothermal method"> hydrothermal method</a>, <a href="https://publications.waset.org/abstracts/search?q=electrode%20material" title=" electrode material"> electrode material</a>, <a href="https://publications.waset.org/abstracts/search?q=specific%20capacitance" title=" specific capacitance"> specific capacitance</a>, <a href="https://publications.waset.org/abstracts/search?q=use%20of%20supercapacitors" title=" use of supercapacitors"> use of supercapacitors</a> </p> <a href="https://publications.waset.org/abstracts/154498/an-electrode-material-for-ultracapacitors-hydrothermal-synthesis-of-neodymium-oxidemanganese-oxidenitrogen-doped-reduced-graphene-oxide-ternary-nanocomposites" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/154498.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">103</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13519</span> Iron Recovery from Red Mud as Zero-Valent Iron Metal Powder Using Direct Electrochemical Reduction Method</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Franky%20Michael%20Hamonangan%20Siagian">Franky Michael Hamonangan Siagian</a>, <a href="https://publications.waset.org/abstracts/search?q=Affan%20Maulana"> Affan Maulana</a>, <a href="https://publications.waset.org/abstracts/search?q=Himawan%20Tri%20Bayu%20Murti%20Petrus"> Himawan Tri Bayu Murti Petrus</a>, <a href="https://publications.waset.org/abstracts/search?q=Widi%20Astuti"> Widi Astuti</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, the feasibility of the direct electrowinning method was used to produce zero-valent iron from red mud. The bauxite residue sample came from the Tayan mine, Indonesia, which contains high hematite (Fe₂O₃). Before electrolysis, the samples were characterized by various analytical techniques (ICP-AES, SEM, XRD) to determine their chemical composition and mineralogy. The direct electrowinning method of red mud suspended in NaOH was introduced at low temperatures ranging from 30 - 110 °C. Variations of current density, red mud: NaOH ratio and temperature were carried out to determine the optimum operation of the direct electrowinning process. Cathode deposits and residues in electrochemical cells were analyzed using XRD, XRF, and SEM to determine the chemical composition and current recovery. The low-temperature electrolysis current efficiency on Redmud can reach 20% recovery at a current density of 920,945 A/m². The moderate performance of the process was investigated with red mud, which was attributed to the troublesome adsorption of red mud particles on the cathode, making the reduction far less efficient than that with hematite. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=red%20mud" title="red mud">red mud</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20reduction" title=" electrochemical reduction"> electrochemical reduction</a>, <a href="https://publications.waset.org/abstracts/search?q=Iron%20production" title=" Iron production"> Iron production</a>, <a href="https://publications.waset.org/abstracts/search?q=hematite" title=" hematite"> hematite</a> </p> <a href="https://publications.waset.org/abstracts/162125/iron-recovery-from-red-mud-as-zero-valent-iron-metal-powder-using-direct-electrochemical-reduction-method" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/162125.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">81</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13518</span> Evaluation of the Inhibitive Effect of Novel Quinoline Schiff Base on Corrosion of Mild Steel in HCl Solution</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Smita%20Jauhari">Smita Jauhari</a>, <a href="https://publications.waset.org/abstracts/search?q=Bhupendra%20Mistry"> Bhupendra Mistry</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Schiff base (E)-2-methyl-N-(tetrazolo[1,5-a]quinolin-4-ylmethylene)aniline (QMA) was synthesized, and its inhibitive effect for mild steel in 1M HCl solution was investigated by weight loss measurement and electrochemical tests.From the weight loss measurements and electrochemical tests, it was observed that the inhibition efficiency increases with the increase in the Schiff base concentration and reaches a maximum at the optimum concentration. This is further confirmed by the decrease in corrosion rate. It is found that the system follows Langmuir adsorption isotherm. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Schiff%20base" title="Schiff base">Schiff base</a>, <a href="https://publications.waset.org/abstracts/search?q=acid%20corrosion" title=" acid corrosion"> acid corrosion</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20impedance%20spectroscopy" title=" electrochemical impedance spectroscopy"> electrochemical impedance spectroscopy</a>, <a href="https://publications.waset.org/abstracts/search?q=polarization" title=" polarization "> polarization </a> </p> <a href="https://publications.waset.org/abstracts/2159/evaluation-of-the-inhibitive-effect-of-novel-quinoline-schiff-base-on-corrosion-of-mild-steel-in-hcl-solution" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/2159.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">372</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13517</span> Iron Recovery from Red Mud As Zero-Valent Iron Metal Powder Using Direct Electrochemical Reduction Method</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Franky%20Michael%20Hamonangan%20Siagian">Franky Michael Hamonangan Siagian</a>, <a href="https://publications.waset.org/abstracts/search?q=Affan%20Maulana"> Affan Maulana</a>, <a href="https://publications.waset.org/abstracts/search?q=Himawan%20Tri%20Bayu%20Murti%20Petrus"> Himawan Tri Bayu Murti Petrus</a>, <a href="https://publications.waset.org/abstracts/search?q=Panut%20Mulyono"> Panut Mulyono</a>, <a href="https://publications.waset.org/abstracts/search?q=Widi%20Astuti"> Widi Astuti</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, the feasibility of the direct electrowinning method was used to produce zero-valent iron from red mud. The bauxite residue sample came from the Tayan mine, Indonesia, which contains high hematite (Fe₂O₃). Before electrolysis, the samples were characterized by various analytical techniques (ICP-AES, SEM, XRD) to determine their chemical composition and mineralogy. The direct electrowinning method of red mud suspended in NaOH was introduced at low temperatures ranging from 30 - 110 °C. Variations of current density, red mud: NaOH ratio and temperature were carried out to determine the optimum operation of the direct electrowinning process. Cathode deposits and residues in electrochemical cells were analyzed using XRD, XRF, and SEM to determine the chemical composition and current recovery. The low-temperature electrolysis current efficiency on Redmud can reach 20% recovery at a current density of 920,945 A/m². The moderate performance of the process was investigated with red mud, which was attributed to the troublesome adsorption of red mud particles on the cathode, making the reduction far less efficient than that with hematite. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=alumina" title="alumina">alumina</a>, <a href="https://publications.waset.org/abstracts/search?q=red%20mud" title=" red mud"> red mud</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20reduction" title=" electrochemical reduction"> electrochemical reduction</a>, <a href="https://publications.waset.org/abstracts/search?q=iron%20production" title=" iron production"> iron production</a> </p> <a href="https://publications.waset.org/abstracts/162943/iron-recovery-from-red-mud-as-zero-valent-iron-metal-powder-using-direct-electrochemical-reduction-method" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/162943.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">86</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13516</span> Hard Carbon Derived From Dextrose as High-Performance Anode Material for Sodium-Ion Batteries</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Rupan%20Das%20Chakraborty">Rupan Das Chakraborty</a>, <a href="https://publications.waset.org/abstracts/search?q=Surendra%20K.%20Martha"> Surendra K. Martha</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Hard carbons (HCs) are extensively used as anode materials for sodium-ion batteries due to their availability, low cost, and ease of synthesis. It possesses the ability to store Na ion between stacked sp2 carbon layers and micropores. In this work, hard carbons are synthesized from different concentrations (0.5M to 5M) of dextrose solutions by hydrothermal synthesis followed by high-temperature calcination at 1100 ⁰C in an inert atmosphere. Dextrose has been chosen as a precursor material as it is a eco-friendly and renewable source. Among all hard carbon derived from different concentrations of dextrose solutions, hard carbon derived from 3M dextrose solution delivers superior electrochemical performance compared to other hard carbons. Hard carbon derived from 3M dextrose solution (Dextrose derived Hard Carbon-3M) provides an initial reversible capacity of 257 mAh g-1 with a capacity retention of 83 % at the end of 100 cycles at 30 mA g-1). The carbons obtained from different dextrose concentration show very similar Cyclic Voltammetry and chargedischarging behavior at a scan rate of 0.05 mV s-1 the Cyclic Voltammetry curve indicate that solvent reduction and the solid electrolyte interface (SEI) formation start at E < 1.2 V (vs Na/Na+). Among all 3M dextrose derived electrode indicate as a promising anode material for Sodium-ion batteries (SIBs). <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=dextrose%20derived%20hard%20carbon" title="dextrose derived hard carbon">dextrose derived hard carbon</a>, <a href="https://publications.waset.org/abstracts/search?q=anode" title=" anode"> anode</a>, <a href="https://publications.waset.org/abstracts/search?q=sodium-ion%20battery" title=" sodium-ion battery"> sodium-ion battery</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20performance" title=" electrochemical performance"> electrochemical performance</a> </p> <a href="https://publications.waset.org/abstracts/167132/hard-carbon-derived-from-dextrose-as-high-performance-anode-material-for-sodium-ion-batteries" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/167132.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">124</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13515</span> Microfluidic Paper-Based Electrochemical Biosensor</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ahmad%20Manbohi">Ahmad Manbohi</a>, <a href="https://publications.waset.org/abstracts/search?q=Seyyed%20Hamid%20Ahmadi"> Seyyed Hamid Ahmadi </a> </p> <p class="card-text"><strong>Abstract:</strong></p> A low-cost paper-based microfluidic device (PAD) for the multiplex electrochemical determination of glucose, uric acid, and dopamine in biological fluids was developed. Using wax printing, PAD containing a central zone, six channels, and six detection zones was fabricated, and the electrodes were printed on detection zones using pre-made electrodes template. For each analyte, two detection zones were used. The carbon working electrode was coated with chitosan-BSA (and enzymes for glucose and uric acid). To detect glucose and uric acid, enzymatic reactions were employed. These reactions involve enzyme-catalyzed redox reactions of the analytes and produce free electrons for electrochemical measurement. Calibration curves were linear (R<sup>&sup2;</sup> &gt; 0.980) in the range of 0-80 mM for glucose, 0.09&ndash;0.9 mM for dopamine, and 0&ndash;50 mM for uric acid, respectively. Blood samples were successfully analyzed by the proposed method. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biological%20fluids" title="biological fluids">biological fluids</a>, <a href="https://publications.waset.org/abstracts/search?q=biomarkers" title=" biomarkers"> biomarkers</a>, <a href="https://publications.waset.org/abstracts/search?q=microfluidic%20paper-based%20electrochemical%20biosensors" title="microfluidic paper-based electrochemical biosensors">microfluidic paper-based electrochemical biosensors</a>, <a href="https://publications.waset.org/abstracts/search?q=Multiplex" title=" Multiplex"> Multiplex</a> </p> <a href="https://publications.waset.org/abstracts/77212/microfluidic-paper-based-electrochemical-biosensor" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/77212.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">286</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13514</span> Electrochemical Study of Ti-O Modified Electrode towards Tyrosinase Catalytic Activity</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Riya%20Thomas">Riya Thomas</a>, <a href="https://publications.waset.org/abstracts/search?q=Denis%20Music"> Denis Music</a>, <a href="https://publications.waset.org/abstracts/search?q=Tautgirdas%20Ruzgas"> Tautgirdas Ruzgas</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The detection of tyrosinase holds considerable interest in the domains of food nutrition and human health due to its significant role in causing a detrimental effect on the colour, flavour, and nutritional value of food as well as in the synthesis of melanin causing skin melanoma. Compared to other conventional analytical techniques, electrochemical (EC) sensors are highly promising owing to their quick response, great sensitivity, ease of use, and low cost. Particularly, titania nanoparticle-based electrochemical sensors have drawn special attention in identifying several biomolecules including enzymes, antibodies, and receptors, owing to their enhanced electrocatalytic activity and electron-accepting properties. In this study, Ti-O film-modified electrode is fabricated using reactive magnetron sputtering, and its affinity towards tyrosinase is examined via electrochemical methods. To comprehend the physiochemical and surface properties-governed electrocatalytic activity of modified electrodes, Ti-O films are grown under various compositional ranges and deposition temperature, and their corresponding electrochemical activity towards tyrosinase is studied. Further, to understand the underlying atomistic mechanisms and electronic-scale electrochemical characteristics, density functional theory (DFT) is employed. The main goal of the current work is to determine the correlation between macroscopic measurements and the underlying atomic properties to improve the tyrosinase activity on Ti-O surfaces. Moreover, this work offers an intriguing new perspective on the use of Ti-O-modified electrodes to detect tyrosinase in the areas of clinical diagnosis, skincare, and food science. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=density%20functional%20theory" title="density functional theory">density functional theory</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20sensor" title=" electrochemical sensor"> electrochemical sensor</a>, <a href="https://publications.waset.org/abstracts/search?q=Ti-O%20film" title=" Ti-O film"> Ti-O film</a>, <a href="https://publications.waset.org/abstracts/search?q=tyrosinase" title=" tyrosinase"> tyrosinase</a> </p> <a href="https://publications.waset.org/abstracts/192153/electrochemical-study-of-ti-o-modified-electrode-towards-tyrosinase-catalytic-activity" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/192153.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">30</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13513</span> Mesocarbon Microbeads Modification of Stainless-Steel Current Collector to Stabilize Lithium Deposition and Improve the Electrochemical Performance of Anode Solid-State Lithium Hybrid Battery</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Abebe%20Taye">Abebe Taye</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The interest in enhancing the performance of all-solid-state batteries featuring lithium metal anodes as a potential alternative to traditional lithium-ion batteries has prompted exploration into new avenues. A promising strategy involves transforming lithium-ion batteries into hybrid configurations by integrating lithium-ion and lithium-metal solid-state components. This study is focused on achieving stable lithium deposition and advancing the electrochemical capabilities of solid-state lithium hybrid batteries with anodes by incorporating mesocarbon microbeads (MCMBs) blended with silver nanoparticles. To achieve this, mesocarbon microbeads (MCMBs) blended with silver nanoparticles are coated on stainless-steel current collectors. These samples undergo a battery of analyses employing diverse techniques. Surface morphology is studied through scanning electron microscopy (SEM). The electrochemical behavior of the coated samples is evaluated in both half-cell and full-cell setups utilizing an argyrodite-type sulfide electrolyte. The stability of MCMBs in the electrolyte is assessed using electrochemical impedance spectroscopy (EIS). Additional insights into the composition are gleaned through X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and energy-dispersive X-ray spectroscopy (EDS). At an ultra-low N/P ratio of 0.26, stability is upheld for over 100 charge/discharge cycles in half-cells. When applied in a full-cell configuration, the hybrid anode preserves 60.1% of its capacity after 80 cycles at 0.3 C under a low N/P ratio of 0.45. In sharp contrast, the capacity retention of the cell using untreated MCMBs declines to 20.2% after a mere 60 cycles. The introduction of mesocarbon microbeads (MCMBs) combined with silver nanoparticles into the hybrid anode of solid-state lithium batteries substantially elevates their stability and electrochemical performance. This approach ensures consistent lithium deposition and removal, mitigating dendrite growth and the accumulation of inactive lithium. The findings from this investigation hold significant value in elevating the reversibility and energy density of lithium-ion batteries, thereby making noteworthy contributions to the advancement of more efficient energy storage systems. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=MCMB" title="MCMB">MCMB</a>, <a href="https://publications.waset.org/abstracts/search?q=lithium%20metal" title=" lithium metal"> lithium metal</a>, <a href="https://publications.waset.org/abstracts/search?q=hybrid%20anode" title=" hybrid anode"> hybrid anode</a>, <a href="https://publications.waset.org/abstracts/search?q=silver%20nanoparticle" title=" silver nanoparticle"> silver nanoparticle</a>, <a href="https://publications.waset.org/abstracts/search?q=cycling%20stability" title=" cycling stability"> cycling stability</a> </p> <a href="https://publications.waset.org/abstracts/171703/mesocarbon-microbeads-modification-of-stainless-steel-current-collector-to-stabilize-lithium-deposition-and-improve-the-electrochemical-performance-of-anode-solid-state-lithium-hybrid-battery" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/171703.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">81</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13512</span> Estimation and Removal of Chlorophenolic Compounds from Paper Mill Waste Water by Electrochemical Treatment</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=R.%20Sharma">R. Sharma</a>, <a href="https://publications.waset.org/abstracts/search?q=S.%20Kumar"> S. Kumar</a>, <a href="https://publications.waset.org/abstracts/search?q=C.%20Sharma"> C. Sharma</a> </p> <p class="card-text"><strong>Abstract:</strong></p> A number of toxic chlorophenolic compounds are formed during pulp bleaching. The nature and concentration of these chlorophenolic compounds largely depends upon the amount and nature of bleaching chemicals used. These compounds are highly recalcitrant and difficult to remove but are partially removed by the biochemical treatment processes adopted by the paper industry. Identification and estimation of these chlorophenolic compounds has been carried out in the primary and secondary clarified effluents from the paper mill by GCMS. Twenty-six chorophenolic compounds have been identified and estimated in paper mill waste waters. Electrochemical treatment is an efficient method for oxidation of pollutants and has successfully been used to treat textile and oil waste water. Electrochemical treatment using less expensive anode material, stainless steel electrodes has been tried to study their removal. The electrochemical assembly comprised a DC power supply, a magnetic stirrer and stainless steel (316 L) electrode. The optimization of operating conditions has been carried out and treatment has been performed under optimized treatment conditions. Results indicate that 68.7% and 83.8% of cholorphenolic compounds are removed during 2 h of electrochemical treatment from primary and secondary clarified effluent respectively. Further, there is a reduction of 65.1, 60 and 92.6% of COD, AOX and color, respectively for primary clarified and 83.8%, 75.9% and 96.8% of COD, AOX and color, respectively for secondary clarified effluent. EC treatment has also been found to increase significantly the biodegradability index of wastewater because of conversion of non- biodegradable fraction into biodegradable fraction. Thus, electrochemical treatment is an efficient method for the degradation of cholorophenolic compounds, removal of color, AOX and other recalcitrant organic matter present in paper mill waste water. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=chlorophenolics" title="chlorophenolics">chlorophenolics</a>, <a href="https://publications.waset.org/abstracts/search?q=effluent" title=" effluent"> effluent</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20treatment" title=" electrochemical treatment"> electrochemical treatment</a>, <a href="https://publications.waset.org/abstracts/search?q=wastewater" title=" wastewater"> wastewater</a> </p> <a href="https://publications.waset.org/abstracts/38459/estimation-and-removal-of-chlorophenolic-compounds-from-paper-mill-waste-water-by-electrochemical-treatment" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/38459.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">392</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13511</span> Biosensors for Parathion Based on Au-Pd Nanoparticles Modified Electrodes</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Tian-Fang%20Kang">Tian-Fang Kang</a>, <a href="https://publications.waset.org/abstracts/search?q=Chao-Nan%20Ge"> Chao-Nan Ge</a>, <a href="https://publications.waset.org/abstracts/search?q=Rui%20Li"> Rui Li</a> </p> <p class="card-text"><strong>Abstract:</strong></p> An electrochemical biosensor for the determination of organophosphorus pesticides was developed based on electrochemical co-deposition of Au and Pd nanoparticles on glassy carbon electrode (GCE). Energy disperse spectroscopy (EDS) analysis was used for characterization of the surface structure. Scanning electron micrograph (SEM) demonstrates that the films are uniform and the nanoclusters are homogeneously distributed on the GCE surface. Acetylcholinesterase (AChE) was immobilized on the Au and Pd nanoparticle modified electrode (Au-Pd/GCE) by cross-linking with glutaraldehyde. The electrochemical behavior of thiocholine at the biosensor (AChE/Au-Pd/GCE) was studied. The biosensors exhibited substantial electrocatalytic effect on the oxidation of thiocholine. The peak current of linear scan voltammetry (LSV) of thiocholine at the biosensor is proportional to the concentration of acetylthiocholine chloride (ATCl) over the range of 2.5 × 10-6 to 2.5 × 10-4 M in 0.1 M phosphate buffer solution (pH 7.0). The percent inhibition of acetylcholinesterase was proportional to the logarithm of parathion concentration in the range of 4.0 × 10-9 to 1.0 × 10-6 M. The detection limit of parathion was 2.6 × 10-9 M. The proposed method exhibited high sensitivity and good reproducibility. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=acetylcholinesterase" title="acetylcholinesterase">acetylcholinesterase</a>, <a href="https://publications.waset.org/abstracts/search?q=Au-Pd%20nanoparticles" title=" Au-Pd nanoparticles"> Au-Pd nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20biosensors" title=" electrochemical biosensors"> electrochemical biosensors</a>, <a href="https://publications.waset.org/abstracts/search?q=parathion" title=" parathion "> parathion </a> </p> <a href="https://publications.waset.org/abstracts/17756/biosensors-for-parathion-based-on-au-pd-nanoparticles-modified-electrodes" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/17756.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">411</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13510</span> Current Approach in Biodosimetry: Electrochemical Detection of DNA Damage</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Marcela%20Jelicova">Marcela Jelicova</a>, <a href="https://publications.waset.org/abstracts/search?q=Anna%20Lierova"> Anna Lierova</a>, <a href="https://publications.waset.org/abstracts/search?q=Zuzana%20Sinkorova"> Zuzana Sinkorova</a>, <a href="https://publications.waset.org/abstracts/search?q=Radovan%20Metelka"> Radovan Metelka</a> </p> <p class="card-text"><strong>Abstract:</strong></p> At present, electrochemical methods are used in various research fields, especially for analysis of biological molecules. The fact offers the possibility of using the detection of oxidative damage induced indirectly by γ rays in DNA in biodosimentry. The main goal of our study is to optimize the detection of 8-hydroxyguanine by differential pulse voltammetry. The level of this stable and specific indicator of DNA damage could be determined in DNA isolated from peripheral blood lymphocytes, plasma or urine of irradiated individuals. Screen-printed carbon electrodes modified with carboxy-functionalized multi-walled carbon nanotubes were utilized for highly sensitive electrochemical detection of 8-hydroxyguanine. Electrochemical oxidation of 8-hydroxoguanine monitored by differential pulse voltammetry was found pH-dependent and the most intensive signal was recorded at pH 7. After recalculating the current density, several times higher sensitivity was attained in comparison with already published results, which were obtained using screen-printed carbon electrodes with unmodified carbon ink. Subsequently, the modified electrochemical technique was used for the detection of 8-hydroxoguanine in calf thymus DNA samples irradiated by 60Co gamma source in the dose range from 0.5 to 20 Gy using by various types of sample pretreatment and measurement conditions. This method could serve for fast retrospective quantification of absorbed dose in cases of accidental exposure to ionizing radiation and may play an important role in biodosimetry. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=biodosimetry" title="biodosimetry">biodosimetry</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20detection" title=" electrochemical detection"> electrochemical detection</a>, <a href="https://publications.waset.org/abstracts/search?q=voltametry" title=" voltametry"> voltametry</a>, <a href="https://publications.waset.org/abstracts/search?q=8-hydroxyguanine" title=" 8-hydroxyguanine"> 8-hydroxyguanine</a> </p> <a href="https://publications.waset.org/abstracts/97358/current-approach-in-biodosimetry-electrochemical-detection-of-dna-damage" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/97358.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">277</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13509</span> Electrochemical Performance of Femtosecond Laser Structured Commercial Solid Oxide Fuel Cells Electrolyte</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Mohamed%20A.%20Baba">Mohamed A. Baba</a>, <a href="https://publications.waset.org/abstracts/search?q=Gazy%20Rodowan"> Gazy Rodowan</a>, <a href="https://publications.waset.org/abstracts/search?q=Brigita%20Abakevi%C4%8Dien%C4%97"> Brigita Abakevičienė</a>, <a href="https://publications.waset.org/abstracts/search?q=Sigitas%20Tamulevi%C4%8Dius"> Sigitas Tamulevičius</a>, <a href="https://publications.waset.org/abstracts/search?q=Bartlomiej%20Lemieszek"> Bartlomiej Lemieszek</a>, <a href="https://publications.waset.org/abstracts/search?q=Sebastian%20Molin"> Sebastian Molin</a>, <a href="https://publications.waset.org/abstracts/search?q=Tomas%20Tamulevi%C4%8Dius"> Tomas Tamulevičius</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Solid oxide fuel cells (SOFC) efficiently convert hydrogen to energy without producing any disturbances or contaminants. The core of the cell is electrolyte. For improving the performance of electrolyte-supported cells, it is desirable to extend the available exchange surface area by micro-structuring of the electrolyte with laser-based micromachining. This study investigated the electrochemical performance of cells micro machined using a femtosecond laser. Commercial ceramic SOFC (Elcogen, AS) with a total thickness of 400 μm was structured by 1030 nm wavelength Yb: KGW fs-laser Pharos (Light Conversion) using 100 kHz repetition frequency and 290 fs pulse length light by scanning with the galvanometer scanner (ScanLab) and focused with a f-Theta telecentric lens (SillOptics). The sample height was positioned using a motorized z-stage. The microstructures were formed using a laser spiral trepanning in Ni/YSZ anode supported membrane at the central part of the ceramic piece of 5.5 mm diameter at active area of the cell. All surface was drilled with 275 µm diameter holes spaced by 275 µm. The machining processes were carried out under ambient conditions. The microstructural effects of the femtosecond laser treatment on the electrolyte surface were investigated prior to the electrochemical characterisation using a scanning electron microscope (SEM) Quanta 200 FEG (FEI). The Novo control Alpha-A was used for electrochemical impedance spectroscopy on a symmetrical cell configuration with an excitation amplitude of 25 mV and a frequency range of 1 MHz to 0.1 Hz. The fuel cell characterization of the cell was examined on open flanges test setup by Fiaxell. Using nickel mesh on the anode side and au mesh on the cathode side, the cell was electrically linked. The cell was placed in a Kittec furnace with a Process IDentifier temperature controller. The wires were connected to a Solartron 1260/1287 frequency analyzer for the impedance and current-voltage characterization. In order to determine the impact of the anode's microstructure on the performance of the commercial cells, the acquired results were compared to cells with unstructured anode. Geometrical studies verified that the depth of the -holes increased linearly according to laser energy and scanning times. On the other hand, it reduced as the scanning speed increased. The electrochemical analysis demonstrates that the open circuit voltage OCV values of the two cells are equal. Further, the modified cell's initial slope reduces to 0.209 from 0.253 of the unmodified cell, revealing that the surface modification considerably decreases energy loss. Plus, the maximum power density for the cell with the microstructure and the reference cell respectively, are 1.45 and 1.16 Wcm⁻². <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20performance" title="electrochemical performance">electrochemical performance</a>, <a href="https://publications.waset.org/abstracts/search?q=electrolyte-supported%20cells" title=" electrolyte-supported cells"> electrolyte-supported cells</a>, <a href="https://publications.waset.org/abstracts/search?q=laser%20micro-structuring" title=" laser micro-structuring"> laser micro-structuring</a>, <a href="https://publications.waset.org/abstracts/search?q=solid%20oxide%20fuel%20cells" title=" solid oxide fuel cells"> solid oxide fuel cells</a> </p> <a href="https://publications.waset.org/abstracts/173757/electrochemical-performance-of-femtosecond-laser-structured-commercial-solid-oxide-fuel-cells-electrolyte" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/173757.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">74</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13508</span> Generation of Value-Added Products from Potato Peels</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Jarina%20Joshi">Jarina Joshi</a>, <a href="https://publications.waset.org/abstracts/search?q=Sarbesh%20Das%20Dangol"> Sarbesh Das Dangol</a>, <a href="https://publications.waset.org/abstracts/search?q=Puja%20Bhatt"> Puja Bhatt</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Potatoes are highly consumed in the country like Nepal. A huge amount of potato peels accumulated daily in households, restaurants and industries. Production of value-added products by degrading waste is a key work in the context of the country where the gross domestic product (GDP) of people is very low. In this study, potato peels are efficiently degraded into various value-added products by electrochemical fermentation of Aspergillus niger (amylase and pectinase-producing strain) which can be a sustainable and economic strategy for solid waste management and product generation. The highest OCV observed in the electrochemical cell using KMnO₄ in catholyte was 1586 ± 63 mV/m³ with anode graphite electrode-coated multi-walled carbon nanotubules. The system in fed-batch mode was found to enhance the performance by adding 10% of the liquid sample every 24 hours. The power density observed with 100-ohm and 1000-ohm external resistors was 119 ± 7 W/m3 and 42 ± 9 W/m³, respectively. From the operation at an optimized condition removal rate of COD, ammoniacal-nitrogen, reducing sugar, and TSS were 37.69%, 67.72%, 72.64%, and 65.95%, respectively. Various value-added products were found to be generated from waste samples, i.e., citric acid, succinic acid, glucose, fructose, propionic acid, etc, with electricity as alternative energy. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=OCV" title="OCV">OCV</a>, <a href="https://publications.waset.org/abstracts/search?q=potato%20peels" title=" potato peels"> potato peels</a>, <a href="https://publications.waset.org/abstracts/search?q=value%20added%20products" title=" value added products"> value added products</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical" title=" electrochemical"> electrochemical</a> </p> <a href="https://publications.waset.org/abstracts/197268/generation-of-value-added-products-from-potato-peels" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/197268.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">12</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13507</span> Dairy Wastewater Remediation Using Electrochemical Oxidation on Boron Doped Diamond (BDD) Anode</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Arwa%20Abdelhay">Arwa Abdelhay</a>, <a href="https://publications.waset.org/abstracts/search?q=Inshad%20Jum%E2%80%99h"> Inshad Jum’h</a>, <a href="https://publications.waset.org/abstracts/search?q=Abeer%20Albsoul"> Abeer Albsoul</a>, <a href="https://publications.waset.org/abstracts/search?q=Khalideh%20Alrawashdeh"> Khalideh Alrawashdeh</a>, <a href="https://publications.waset.org/abstracts/search?q=Dina%20Al%20Tarazi"> Dina Al Tarazi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Treated wastewater reuse has been considered recently as one of the successful management strategies to overcome water shortage in countries suffering from water scarcity. The non-readily biodegradable and recalcitrant pollutants in wastewater cannot be destructed by conventional treatment methods. This paper deals with the electrochemical treatment of dairy wastewater using a promising non-conventional Boron-Doped Diamond (BDD) anode. During the electrochemical process, different operating parameters were investigated, such as electrolysis time, current density, supporting electrolyte, chemical oxygen demand (COD), turbidity as well as absorbance/color. The experimental work revealed that electrochemical oxidation carried out with no added electrolyte has significantly reduced the COD, turbidity, and color (absorbance) by 72%, 76%, and 78% respectively. Results also showed that raising the current density from 5.1 mA/cm² to 7.7 mA/cm² has boosted COD, and color removal to 82.5%, and 83% respectively. However, the current density did not show any significant effect on the turbidity. Interestingly, it was observed that adding Na₂SO₄ and FeCl₃ as supporting electrolytes brought the COD removal to 91% and 97% respectively. Likewise, turbidity and color removal has been enhanced by the addition of the same supporting electrolytes. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=boron%20doped-diamond%20anode" title="boron doped-diamond anode">boron doped-diamond anode</a>, <a href="https://publications.waset.org/abstracts/search?q=dairy%20wastewater" title=" dairy wastewater"> dairy wastewater</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20oxidation" title=" electrochemical oxidation"> electrochemical oxidation</a>, <a href="https://publications.waset.org/abstracts/search?q=supporting%20electrolytes" title=" supporting electrolytes"> supporting electrolytes</a> </p> <a href="https://publications.waset.org/abstracts/92414/dairy-wastewater-remediation-using-electrochemical-oxidation-on-boron-doped-diamond-bdd-anode" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/92414.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">163</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13506</span> Electrochemical Detection of Polycyclic Aromatic Hydrocarbons in Urban Air by Exfoliated Graphite Based Electrode</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=A.%20Sacko">A. Sacko</a>, <a href="https://publications.waset.org/abstracts/search?q=H.%20Nyoni"> H. Nyoni</a>, <a href="https://publications.waset.org/abstracts/search?q=T.%20A.%20M.%20Msagati"> T. A. M. Msagati</a>, <a href="https://publications.waset.org/abstracts/search?q=B.%20Ntsendwana"> B. Ntsendwana</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Carbon based materials to target environmental pollutants have become increasingly recognized in science. Electrochemical methods using carbon based materials are notable methods for high sensitive detection of organic pollutants in air. It is therefore in this light that exfoliated graphite electrode was fabricated for electrochemical analysis of PAHs in urban atmospheric air. The electrochemical properties of the graphite electrode were studied using CV and EIS in the presence of acetate buffer supporting electrolyte with 2 Mm ferricyanide as a redox probe. The graphite electrode showed enhanced current response which confirms facile kinetics and enhanced sensitivity. However, the peak to peak (DE) separation increased as a function of scan rate. The EIS showed a high charger transfer resistance. The detection phenanthrene on the exfoliated graphite was studied in the presence of acetate buffer solution at PH 3.5 using DPV. The oxidation peak of phenanthrene was observed at 0.4 V. Under optimized conditions (supporting electrolyte, pH, deposition time, etc.). The detection limit observed was at 5x 10⁻⁸ M. Thus the results demonstrate with further optimization and modification lower concentration detection can be achieved. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20detection" title="electrochemical detection">electrochemical detection</a>, <a href="https://publications.waset.org/abstracts/search?q=exfoliated%20graphite" title=" exfoliated graphite"> exfoliated graphite</a>, <a href="https://publications.waset.org/abstracts/search?q=PAHs%20%28polycyclic%20aromatic%20hydrocarbons%29" title=" PAHs (polycyclic aromatic hydrocarbons)"> PAHs (polycyclic aromatic hydrocarbons)</a>, <a href="https://publications.waset.org/abstracts/search?q=urban%20air" title=" urban air"> urban air</a> </p> <a href="https://publications.waset.org/abstracts/78454/electrochemical-detection-of-polycyclic-aromatic-hydrocarbons-in-urban-air-by-exfoliated-graphite-based-electrode" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/78454.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">213</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13505</span> Emulsified Oil Removal in Produced Water by Graphite-Based Adsorbents Using Adsorption Coupled with Electrochemical Regeneration</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zohreh%20Fallah">Zohreh Fallah</a>, <a href="https://publications.waset.org/abstracts/search?q=Edward%20P.%20L.%20Roberts"> Edward P. L. Roberts</a> </p> <p class="card-text"><strong>Abstract:</strong></p> One of the big challenges for produced water treatment is removing oil from water in the form of emulsified droplets which are not easily separated. An attractive approach is adsorption, as it is a simple and effective process. However, adsorbents must be regenerated in order to make the process cost effective. Several sorbents have been tested for treating oily wastewater. However, some issues such as high energy consumption for activated carbon thermal regeneration have been reported. Due to their significant electrical conductivity, Graphite Intercalation Compounds (GIC) were found to be suitable to be regenerated electrochemically. They are non-porous materials with low surface area and fast adsorptive capacity which are useful for removal of low concentration of organics. An innovative adsorption/regeneration process has been developed at the University of Manchester in which adsorption of organics are done by using a patented GIC adsorbent coupled with subsequent electrochemical regeneration. The oxidation of adsorbed organics enables 100% regeneration so that the adsorbent can be reused over multiple adsorption cycles. GIC adsorbents are capable of removing a wide range of organics and pollutants; however, no comparable report is available for removal of emulsified oil in produced water using abovementioned process. In this study the performance of this technology for the removal of emulsified oil in wastewater was evaluated. Batch experiments were carried out to determine the adsorption kinetics and equilibrium isotherm for both real produced water and model emulsions. The amount of oil in wastewater was measured by using the toluene extraction/fluorescence analysis before and after adsorption and electrochemical regeneration cycles. It was found that oil in water emulsion could be successfully treated by the treatment process and More than 70% of oil was removed. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=adsorption" title="adsorption">adsorption</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20regeneration" title=" electrochemical regeneration"> electrochemical regeneration</a>, <a href="https://publications.waset.org/abstracts/search?q=emulsified%20oil" title=" emulsified oil"> emulsified oil</a>, <a href="https://publications.waset.org/abstracts/search?q=produced%20water" title=" produced water"> produced water</a> </p> <a href="https://publications.waset.org/abstracts/29358/emulsified-oil-removal-in-produced-water-by-graphite-based-adsorbents-using-adsorption-coupled-with-electrochemical-regeneration" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/29358.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">586</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13504</span> Green Electrochemical Nitration of Bioactive Compounds: Biological Evaluation with Molecular Modelling</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Sara%20Torabi">Sara Torabi</a>, <a href="https://publications.waset.org/abstracts/search?q=Sadegh%20Khazalpour"> Sadegh Khazalpour</a>, <a href="https://publications.waset.org/abstracts/search?q=Mahdi%20Jamshidi"> Mahdi Jamshidi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Nitro aromatic compounds are valuable materials because of their applications in the preparation of chemical intermediates for the synthesis of dyes, plastics, perfumes, energetic materials, and pharmaceuticals. Chemical and electrochemical procedures are reported for nitration of aromatic compounds. Flavonoid derivatives are present in many vegetables and fruits and are constituent of many common pharmaceuticals and dietary supplements. Electrochemistry provides very versatile means for the electrosynthesis, mechanistic and kinetic studies. To the best of our knowledge, and despite the importance of these compounds in numerous scientific fields, there are no reports on the electrochemical nitration of Quercetin derivatives. Herein, we describe a green electrochemical synthesis of a nitro compound. In this work, electrochemical oxidation of Quercetin has been studied in the presence of nitrite ion as a nucleophile in acetate buffer solution (c = 0.2 M, pH = 6.0), by means of cyclic voltammetry and controlled-potential coulometry. The results indicate the participation of produced o-benzoquinones in Michael reaction with nitrite ion (in the divided cell) to form the corresponding nitro diol (EC mechanism). The purity of product and characterization was done using ¹H NMR, ¹³C NMR, FTIR spectroscopic techniques. The presented strategies use a water/ethanol mixture as solvent. Ethanol as cosolvent was also used in the previous studies because of its low cost, safety, easy availability, recyclability, bioproductability, and biodegradability. These strategies represent a one-pot and facile process for the synthesis of nitro compound in high yield and purity under green conditions. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20synthesis" title="electrochemical synthesis">electrochemical synthesis</a>, <a href="https://publications.waset.org/abstracts/search?q=green%20chemistry" title=" green chemistry"> green chemistry</a>, <a href="https://publications.waset.org/abstracts/search?q=cyclic%20voltammetry" title=" cyclic voltammetry"> cyclic voltammetry</a>, <a href="https://publications.waset.org/abstracts/search?q=molecular%20docking" title=" molecular docking"> molecular docking</a> </p> <a href="https://publications.waset.org/abstracts/133449/green-electrochemical-nitration-of-bioactive-compounds-biological-evaluation-with-molecular-modelling" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/133449.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">148</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13503</span> Designing Nickel Coated Activated Carbon (Ni/AC) Based Electrode Material for Supercapacitor Applications</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Zahid%20Ali%20Ghazi">Zahid Ali Ghazi</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Supercapacitors (SCs) have emerged as auspicious energy storage devices because of their fast charge-discharge characteristics and high power densities. In the current study, a simple approach is used to coat activated carbon (AC) with a thin layer of nickel (Ni) by an electroless deposition process to enhance the electrochemical performance of the SC. The synergistic combination of large surface area and high electrical conductivity of the AC, as well as the pseudocapacitive behavior of the metallic Ni, has shown great potential to overcome the limitations of traditional SC materials. First, the materials were characterized using X-ray diffraction (XRD) for crystallography, scanning electron microscopy (SEM) for surface morphology and energy dispersion X-ray (EDX) for elemental analysis. The electrochemical performance of the nickel-coated activated carbon (Ni-AC) is systematically evaluated through various techniques, including galvanostatic charge-discharge (GCD), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). The GCD results revealed that Ni/AC has a higher specific capacitance (1559 F/g) than bare AC (222 F/g) at 1 A/g current density in a 2 M KOH electrolyte. Even at a higher current density of 20 A/g, the Ni/AC showed a high capacitance of 944 F/g as compared to 77 F/g by AC. The specific capacitance (1318 F/g) calculated from CV measurements for Ni-AC at 10mV/sec was in close agreement with GCD data. Furthermore, the bare AC exhibited a low energy of 15 Wh/kg at a power density of 356 W/kg whereas, an energy density of 111 Wh/kg at a power density of 360 W/kg was achieved by Ni/AC-850 electrode and demonstrated a long life cycle with 94% capacitance retention over 50000 charge/discharge cycles at 10 A/g. In addition, the EIS study disclosed that the Rs and Rct values of Ni/AC electrodes were much lower than those of bare AC. The superior performance of Ni/AC is mainly attributed to the presence of excessive redox active sites, large electroactive surface area and corrosive resistance properties of Ni. We believe that this study will provide new insights into the controlled coating of ACs and other porous materials with metals for developing high-performance SCs and other energy storage devices. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=supercapacitor" title="supercapacitor">supercapacitor</a>, <a href="https://publications.waset.org/abstracts/search?q=cyclic%20voltammetry" title=" cyclic voltammetry"> cyclic voltammetry</a>, <a href="https://publications.waset.org/abstracts/search?q=coating" title=" coating"> coating</a>, <a href="https://publications.waset.org/abstracts/search?q=energy%20density" title=" energy density"> energy density</a>, <a href="https://publications.waset.org/abstracts/search?q=activated%20carbon" title=" activated carbon"> activated carbon</a> </p> <a href="https://publications.waset.org/abstracts/175609/designing-nickel-coated-activated-carbon-niac-based-electrode-material-for-supercapacitor-applications" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/175609.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">70</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13502</span> Effective Doping Engineering of Na₃V₂(PO₄)₂F₃ as a High-Performance Cathode Material for Sodium-Ion Batteries</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ramon%20Alberto%20Paredes%20Camacho">Ramon Alberto Paredes Camacho</a>, <a href="https://publications.waset.org/abstracts/search?q=Li%20Lu"> Li Lu</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Sustainable batteries are possible through the development of cheaper and greener alternatives whose most feasible option is epitomized by Sodium-Ion Batteries (SIB). Na₃V₂(PO₄)₂F₃ (NVPF) an important member of the Na-superionic-conductor (NASICON) materials, has recently been in the spotlight due to its interesting electrochemical properties when used as cathode namely, high specific capacity of 128 mA h g-¹, high energy density of 507 W h Kg-¹, increased working potential at which vanadium redox couples can be activated (with an average value around 3.9 V), and small volume variation of less than 2%. These traits grant NVPF an excellent perspective as a cathode material for the next generation of sodium batteries. Unfortunately, because of its low inherent electrical conductivity and a high energy barrier that impedes the mobilization of all the available Na ions per formula, the overall electrochemical performance suffers substantial degradation, finally obstructing its industrial use. Many approaches have been developed to remediate these issues where nanostructural design, carbon coating, and ion doping are the most effective ones. This investigation is focused on enhancing the electrochemical response of NVPF by doping metal ions in the crystal lattice, substituting vanadium atoms. A facile sol-gel process is employed, with citric acid as the chelator and the carbon source. The optimized conditions circumvent fluorine sublimation, ratifying the material’s purity. One of the reasons behind the large ionic improvement is the attraction of extra Na ions into the crystalline structure due to a charge imbalance produced by the valence of the doped ions (+2), which is lower than the one of vanadium (+3). Superior stability (higher than 90% at a current density of 20C) and capacity retention at an extremely high current density of 50C are demonstrated by our doped NVPF. This material continues to retain high capacity values at low and high temperatures. In addition, full cell NVPF//Hard Carbon shows capacity values and high stability at -20 and 60ºC. Our doping strategy proves to significantly increase the ionic and electronic conductivity of NVPF even at extreme conditions, delivering outstanding electrochemical performance and paving the way for advanced high-potential cathode materials. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=sodium-ion%20batteries" title="sodium-ion batteries">sodium-ion batteries</a>, <a href="https://publications.waset.org/abstracts/search?q=cathode%20materials" title=" cathode materials"> cathode materials</a>, <a href="https://publications.waset.org/abstracts/search?q=NASICON" title=" NASICON"> NASICON</a>, <a href="https://publications.waset.org/abstracts/search?q=Na3V2%28PO4%292F3" title=" Na3V2(PO4)2F3"> Na3V2(PO4)2F3</a>, <a href="https://publications.waset.org/abstracts/search?q=Ion%20doping" title=" Ion doping"> Ion doping</a> </p> <a href="https://publications.waset.org/abstracts/178243/effective-doping-engineering-of-na3v2po42f3-as-a-high-performance-cathode-material-for-sodium-ion-batteries" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/178243.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">62</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13501</span> Combination of Electrochemical Impedance Spectroscopy and Electromembrane Extraction for the Determination of Zolpidem Using Modified Screen-Printed Electrode</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Ali%20Naeemy">Ali Naeemy</a>, <a href="https://publications.waset.org/abstracts/search?q=Mir%20Ghasem%20Hoseini"> Mir Ghasem Hoseini</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, for the first time, an analytical method developed and validated by combining electrochemical impedance spectroscopy and electromembrane extraction (EIS-EME) by Vulcan/poly pyrrole nanocomposite modified screen-printed electrode (PPY–VU/SPE) for accurately quantifying zolpidem. EME parameters optimized, including solvent composition, voltage, pH adjustments and extraction time. Zolpidem was transferred from a donor solution (pH 5) to an acceptor solution (pH 13) using a hollow fiber in 1-octanol as a membrane, driven by a 60 V voltage for 25 minutes, ensuring precise and selective extraction. In comparison with SPE, VU/SPE and PPY/SPE, the PPY–VU/SPE was much more efficient for ZP oxidation. Calibration curves with good linearity were obtained in the concentration range of 2-75 µmol L-1 using the EIS-EME with the detection limit of 0.5 µmol L-1 . Finally, the EIS-EME by using the PPY– VU/SPE was successfully used to determine ZP in tablet dosage form, urine and plasma samples. Keywords: Electrochemical impedance spectroscopy, Electromembrane extraction, Zolpidem, Vulcan, poly pyrrole, Screen printed electrode <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20impedance%20spectroscopy" title="electrochemical impedance spectroscopy">electrochemical impedance spectroscopy</a>, <a href="https://publications.waset.org/abstracts/search?q=electromembrane%20extraction" title=" electromembrane extraction"> electromembrane extraction</a>, <a href="https://publications.waset.org/abstracts/search?q=screen%20printed%20electrode" title=" screen printed electrode"> screen printed electrode</a>, <a href="https://publications.waset.org/abstracts/search?q=zolpidem" title=" zolpidem"> zolpidem</a> </p> <a href="https://publications.waset.org/abstracts/186746/combination-of-electrochemical-impedance-spectroscopy-and-electromembrane-extraction-for-the-determination-of-zolpidem-using-modified-screen-printed-electrode" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/186746.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">47</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13500</span> Hybrid Graphene Based Nanomaterial as Highly Efficient Catalyst for the Electrochemical Determination of Ciprofloxacin</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Tien%20S.%20H.%20Pham">Tien S. H. Pham</a>, <a href="https://publications.waset.org/abstracts/search?q=Peter%20J.%20Mahon"> Peter J. Mahon</a>, <a href="https://publications.waset.org/abstracts/search?q=Aimin%20Yu"> Aimin Yu</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The detection of drug molecules by voltammetry has attracted great interest over the past years. However, many drug molecules exhibit poor electrochemical signals at common electrodes which result in low sensitivity in detection. An efficient way to overcome this problem is to modify electrodes with functional materials. Since discovered in 2004, graphene (or reduced graphene oxide) has emerged as one of the most studied two-dimensional carbon materials in condensed matter physics, electrochemistry, and so on due to its exceptional physicochemical properties. Additionally, the continuous development of technology has opened the new window for the successful fabrications of many novel graphene-based nanomaterials to serve in electrochemical analysis. This research aims to synthesize and characterize gold nanoparticle coated beta-cyclodextrin functionalized reduced graphene oxide (Au NP–β-CD–RGO) nanocomposites with highly conductive and strongly electro-catalytic properties as well as excellent supramolecular recognition abilities for the modification of electrodes. The electrochemical responses of ciprofloxacin at the as-prepared nanocomposite modified electrode was effectively amplified was much higher in comparison with that at the bare electrode. The linear concentration range was from 0.01 to 120 µM, with a detection limit of 2.7 nM using differential pulse voltammetry. Thus, Au NP–β-CD–RGO nanocomposite has great potential as an ideal material to construct sensitive sensors for the electrochemical determination of ciprofloxacin or similar antibacterial drugs in the future based on its excellent stability, selectivity, and reproducibility. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=Au%20nanoparticles" title="Au nanoparticles">Au nanoparticles</a>, <a href="https://publications.waset.org/abstracts/search?q=%CE%B2-CD" title=" β-CD"> β-CD</a>, <a href="https://publications.waset.org/abstracts/search?q=ciprofloxacin" title=" ciprofloxacin"> ciprofloxacin</a>, <a href="https://publications.waset.org/abstracts/search?q=electrochemical%20determination" title=" electrochemical determination"> electrochemical determination</a>, <a href="https://publications.waset.org/abstracts/search?q=graphene%20based%20nanomaterials" title=" graphene based nanomaterials"> graphene based nanomaterials</a> </p> <a href="https://publications.waset.org/abstracts/73614/hybrid-graphene-based-nanomaterial-as-highly-efficient-catalyst-for-the-electrochemical-determination-of-ciprofloxacin" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/73614.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">191</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13499</span> Polypyrrole Integrated MnCo2O4 Nanorods Hybrid as Electrode Material for High Performance Supercapacitor</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Santimoy%20Khilari">Santimoy Khilari</a>, <a href="https://publications.waset.org/abstracts/search?q=Debabrata%20Pradhan"> Debabrata Pradhan</a> </p> <p class="card-text"><strong>Abstract:</strong></p> Ever−increasing energy demand and growing energy crisis along with environmental issues emphasize the research on sustainable energy conversion and storage systems. Recently, supercapacitors or electrochemical capacitors emerge as a promising energy storage technology for future generation. The activity of supercapacitors generally depends on the efficiency of its electrode materials. So, the development of cost−effective efficient electrode materials for supercapacitors is one of the challenges to the scientific community. Transition metal oxides with spinel crystal structure receive much attention for different electrochemical applications in energy storage/conversion devices because of their improved performance as compared to simple oxides. In the present study, we have synthesized polypyrrole (PPy) supported manganese cobaltite nanorods (MnCo2O4 NRs) hybrid electrode material for supercapacitor application. The MnCo2O4 NRs were synthesized by a simple hydrothermal and calcination approach. The MnCo2O4 NRs/PPy hybrid was prepared by in situ impregnation of MnCo2O4 NRs during polymerization of pyrrole. The surface morphology and microstructure of as−synthesized samples was characterized by scanning electron microscopy and transmission electron microscopy, respectively. The crystallographic phase of MnCo2O4 NRs, PPy and hybrid was determined by X-ray diffraction. Electrochemical charge storage activity of MnCo2O4 NRs, PPy and MnCo2O4 NRs/PPy hybrid was evaluated from cyclic voltammetry, chronopotentiometry and electrochemical impedance spectroscopy. Significant improvement of specific capacitance was achieved in MnCo2O4 NRs/PPy hybrid as compared to the individual components. Furthermore, the mechanically mixed MnCo2O4 NRs, and PPy shows lower specific capacitance as compared to MnCo2O4 NRs/PPy hybrid suggesting the importance of in situ hybrid preparation. The stability of as prepared electrode materials was tested by cyclic charge-discharge measurement for 1000 cycles. Maximum 94% capacitance was retained with MnCo2O4 NRs/PPy hybrid electrode. This study suggests that MnCo2O4 NRs/PPy hybrid can be used as a low cost electrode material for charge storage in supercapacitors. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=supercapacitors" title="supercapacitors">supercapacitors</a>, <a href="https://publications.waset.org/abstracts/search?q=nanorods" title=" nanorods"> nanorods</a>, <a href="https://publications.waset.org/abstracts/search?q=spinel" title=" spinel"> spinel</a>, <a href="https://publications.waset.org/abstracts/search?q=MnCo2O4" title=" MnCo2O4"> MnCo2O4</a>, <a href="https://publications.waset.org/abstracts/search?q=polypyrrole" title=" polypyrrole"> polypyrrole</a> </p> <a href="https://publications.waset.org/abstracts/14163/polypyrrole-integrated-mnco2o4-nanorods-hybrid-as-electrode-material-for-high-performance-supercapacitor" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/14163.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">345</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13498</span> Carbon-Based Electrochemical Detection of Pharmaceuticals from Water</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=M.%20Ardelean">M. Ardelean</a>, <a href="https://publications.waset.org/abstracts/search?q=F.%20Manea"> F. Manea</a>, <a href="https://publications.waset.org/abstracts/search?q=A.%20Pop"> A. Pop</a>, <a href="https://publications.waset.org/abstracts/search?q=J.%20Schoonman"> J. Schoonman</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The presence of pharmaceuticals in the environment and especially in water has gained increasing attention. They are included in emerging class of pollutants, and for most of them, legal limits have not been set-up due to their impact on human health and ecosystem was not determined and/or there is not the advanced analytical method for their quantification. In this context, the development of various advanced analytical methods for the quantification of pharmaceuticals in water is required. The electrochemical methods are known to exhibit the great potential for high-performance analytical methods but their performance is in direct relation to the electrode material and the operating techniques. In this study, two types of carbon-based electrodes materials, i.e., boron-doped diamond (BDD) and carbon nanofiber (CNF)-epoxy composite electrodes have been investigated through voltammetric techniques for the detection of naproxen in water. The comparative electrochemical behavior of naproxen (NPX) on both BDD and CNF electrodes was studied by cyclic voltammetry, and the well-defined peak corresponding to NPX oxidation was found for each electrode. NPX oxidation occurred on BDD electrode at the potential value of about +1.4 V/SCE (saturated calomel electrode) and at about +1.2 V/SCE for CNF electrode. The sensitivities for NPX detection were similar for both carbon-based electrode and thus, CNF electrode exhibited superiority in relation to the detection potential. Differential-pulsed voltammetry (DPV) and square-wave voltammetry (SWV) techniques were exploited to improve the electroanalytical performance for the NPX detection, and the best results related to the sensitivity of 9.959 &micro;A&middot;&micro;M<sup>-1</sup> were achieved using DPV. In addition, the simultaneous detection of NPX and fluoxetine -a very common antidepressive drug, also present in water, was studied using CNF electrode and very good results were obtained. The detection potential values that allowed a good separation of the detection signals together with the good sensitivities were appropriate for the simultaneous detection of both tested pharmaceuticals. These results reclaim CNF electrode as a valuable tool for the individual/simultaneous detection of pharmaceuticals in water. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=boron-doped%20diamond%20electrode" title="boron-doped diamond electrode">boron-doped diamond electrode</a>, <a href="https://publications.waset.org/abstracts/search?q=carbon%20nanofiber-epoxy%20composite%20electrode" title=" carbon nanofiber-epoxy composite electrode"> carbon nanofiber-epoxy composite electrode</a>, <a href="https://publications.waset.org/abstracts/search?q=emerging%20pollutans" title=" emerging pollutans"> emerging pollutans</a>, <a href="https://publications.waset.org/abstracts/search?q=pharmaceuticals" title=" pharmaceuticals"> pharmaceuticals</a> </p> <a href="https://publications.waset.org/abstracts/50194/carbon-based-electrochemical-detection-of-pharmaceuticals-from-water" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/50194.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">284</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13497</span> Electrochemical Treatment and Chemical Analyses of Tannery Wastewater Using Sacrificial Aluminum Electrode, Ethiopia</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Dessie%20Tibebe">Dessie Tibebe</a>, <a href="https://publications.waset.org/abstracts/search?q=Muluken%20Asmare"> Muluken Asmare</a>, <a href="https://publications.waset.org/abstracts/search?q=Marye%20Mulugeta"> Marye Mulugeta</a>, <a href="https://publications.waset.org/abstracts/search?q=Yezbie%20Kassa"> Yezbie Kassa</a>, <a href="https://publications.waset.org/abstracts/search?q=Zerubabel%20Moges"> Zerubabel Moges</a>, <a href="https://publications.waset.org/abstracts/search?q=Dereje%20Yenealem"> Dereje Yenealem</a>, <a href="https://publications.waset.org/abstracts/search?q=Tarekegn%20Fentie"> Tarekegn Fentie</a>, <a href="https://publications.waset.org/abstracts/search?q=Agmas%20Amare"> Agmas Amare</a> </p> <p class="card-text"><strong>Abstract:</strong></p> The performance of electrocoagulation (EC) using Aluminium electrodes for the treatment of effluent-containing chromium metal using a fixed bed electrochemical batch reactor was studied. In the present work, the efficiency evaluation of EC in removing physicochemical and heavy metals from real industrial tannery wastewater in the Amhara region, collected from Bahirdar, Debre Brihan, and Haik, was investigated. The treated and untreated samples were determined by AAS and ICP OES spectrophotometers. The results indicated that selected heavy metals were removed in all experiments with high removal percentages. The optimal results were obtained regarding both cost and electrocoagulation efficiency with initial pH = 3, initial concentration = 40 mg/L, electrolysis time = 30 min, current density = 40 mA/cm2, and temperature = 25oC favored metal removal. The maximum removal percentages of selected metals obtained were 84.42% for Haik, 92.64% for Bahir Dar and 94.90% for Debre Brihan. The sacrificial electrode and sludge were characterized by FT-IR, SEM and XRD. After treatment, some metals like chromium will be used again as a tanning agent in leather processing to promote a circular economy. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=electrochemical" title="electrochemical">electrochemical</a>, <a href="https://publications.waset.org/abstracts/search?q=treatment" title=" treatment"> treatment</a>, <a href="https://publications.waset.org/abstracts/search?q=aluminum" title=" aluminum"> aluminum</a>, <a href="https://publications.waset.org/abstracts/search?q=tannery%20effluent" title=" tannery effluent"> tannery effluent</a> </p> <a href="https://publications.waset.org/abstracts/174363/electrochemical-treatment-and-chemical-analyses-of-tannery-wastewater-using-sacrificial-aluminum-electrode-ethiopia" class="btn btn-primary btn-sm">Procedia</a> <a href="https://publications.waset.org/abstracts/174363.pdf" target="_blank" class="btn btn-primary btn-sm">PDF</a> <span class="bg-info text-light px-1 py-1 float-right rounded"> Downloads <span class="badge badge-light">124</span> </span> </div> </div> <div class="card paper-listing mb-3 mt-3"> <h5 class="card-header" style="font-size:.9rem"><span class="badge badge-info">13496</span> CuFeOx-Based Nano-Rose Electrocatalysts for Oxygen Evolution Reaction</h5> <div class="card-body"> <p class="card-text"><strong>Authors:</strong> <a href="https://publications.waset.org/abstracts/search?q=Hamad%20Almohamadi">Hamad Almohamadi</a>, <a href="https://publications.waset.org/abstracts/search?q=Nabeel%20H.%20Alharthi"> Nabeel H. Alharthi</a>, <a href="https://publications.waset.org/abstracts/search?q=Abdulrahman%20Aljabri"> Abdulrahman Aljabri</a> </p> <p class="card-text"><strong>Abstract:</strong></p> In this study, two-dimensional CuFeOx is deposited on nickel foam for the fabrication of electrocatalyst for oxygen evolution reaction (OER). The in-situ hydrothermal synthesis of CuFeOx in presence of aloe vera extract was found to yield unique nano-rose-like morphology which aided to improve the electrochemical surface area of the electrode. The phytochemical assisted synthesis of CuFeOx using 75% aloe vera extract resulted in improved OER electrocatalytic performance by attaining the overpotential of 310 mV for 50 mA cm−2 and 410 mV for 100 mA cm−2. The electrode also sustained robust stability throughout the 50 h of chronopotentiometry studies under alkaline electrolyte conditions, thus proving to be prospective electrode material for efficient OER in electrochemical water splitting. <p class="card-text"><strong>Keywords:</strong> <a href="https://publications.waset.org/abstracts/search?q=water%20splitting" title="water splitting">water splitting</a>, <a href="https://publications.waset.org/abstracts/search?q=phytochemicals" title=" phytochemicals"> phytochemicals</a>, <a href="https://publications.waset.org/abstracts/search?q=oxygen%20evaluation%20reaction" title=" oxygen evaluation reaction"> oxygen evaluation reaction</a>, <a href="https://publications.waset.org/abstracts/search?q=Tafel%27s%20slope" title=" Tafel&#039;s slope"> Tafel&#039;s slope</a>, <a href="https://publications.waset.org/abstracts/search?q=stability" title=" stability"> stability</a> </p> <a 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