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Interface 1000 electrochemical workstation

Manufactured by Gamry
Sourced in United States

The Interface 1000 is an electrochemical workstation designed for fundamental electrochemical measurements. It provides potentiostatic and galvanostatic control for a wide range of electrochemical techniques.

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4 protocols using interface 1000 electrochemical workstation

1

Potentiometric Measurements and Thermal Expansion of Glass-Ceramic Composites

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All potentiometric measurements were performed in stirred solutions at room temperature (25 °C) with an eight-channel electrode-computer interface (Nico2000 Ltd, UK) controlled by Nico-2000 software. A free flow single-junction Ag/AgCl reference electrode purchased from Thermo-Fisher (USA) was used as an external reference electrode. The pH measurements were performed using EDWA (Romania) combined glass electrode. Thermal expansion coefficients were measured using optical dilatometry (Misura® HSM ODHT 1400, Italy). Milling was performed using laboratory fast mill Mod Speedy from Nannetti (Italy). All impedance measurements were performed using an interface-1000 electrochemical workstation from Gamry (USA). The impedance of the porous frits was determined by impedance spectroscopy using two-electrode system measurement using Gamry-1000 potentiostat (USA). Morphological analysis of the prepared glass–ceramic composite-based frits was performed using a field emission scanning electron microscope (FESEM) (FEI Quanta 250 FEG model).
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2

Electrochemical Corrosion Analysis of Steel and Ni-based Alloy

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An Interface 1000 electrochemical workstation (Gamry Instruments, Warminster, PA, USA) was used for electrochemical measurements. A three-electrode electrochemical cell was used with a platinum plate as a counter electrode and a saturated calomel electrode (SCE) as a reference electrode. BG90SS steel and the Ni-based alloy coating specimens were respectively employed as the working electrode (WE). After the WE was immersed in the solution for 30 min to obtain a stable open circuit potential (OCP), the potentiodynamic polarization curve was carried out in a range of −500 mV–1000 mV with respect to the corrosion potential, and with a scan rate of 0.5 mV/s. All the potentials in this study referred to this reference electrode.
The test solution to simulate the formation water from a gas condensate field in China was made up of analytical grade reagents and deionized water. The chemical composition of the test solution is listed in Table 2. Prior to the tests, the solution was purged with N2 (99.99%) for at least 4 h, and then the test solution was saturated with H2S/CO2 mixed gases at a speed of 200 mL/min for 1 h. Afterwards, the WE was immersed in the solution, and the H2S/CO2 mixed gases were then bubbled through the solution at a low flow rate of 20 mL/min. The tests were performed under static conditions at 25 °C and atmospheric pressure (H2S/CO2 pressure was 0.1 MPa).
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3

Electrochemical Characterization of t-CN@Cu Anode

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The electrochemical
characterizations
were conducted using the Biologic MPG-2 Battery Testing System at
room temperature. Galvanostatic cycling tests were measured in two-electrode
cells, first discharged-charged at a constant current density of 0.1
mA cm–2 within a voltage window of 2.0 to 0.0 V
(vs Li+/Li) for five initial formation cycles and then
discharged at a certain content current density (i.e., 0.2, 0.5, 1.0,
or 2.0 mA cm–2) under constant capacity conditions
(i.e., 0.5, 1.0, 2.0, or 5.0 mAh cm–2) in subsequent
cycles. The electrochemical impedance spectroscopy (EIS) was recorded
by using three-electrode cells in a frequency range from 100 mHz to
100 kHz. The ex situ EIS curves of the t-CN@Cu electrode were collected
at various selected SOCs during the first formation cycle. The galvanostatic
intermittent titration technique (GITT) was measured with a polarization
process consisting of a current pulse of 0.1 mA cm–2 for 10 min followed by an open circuit stand process for 60 min
to relax to quasiequilibrium potential. The detailed calculation of
Li+ chemical diffusion coefficients is shown in Supporting Information. The Tafel plots were
obtained on a Gamry Interface 1000 electrochemical workstation at
a scan rate of 0.1 mV s–1 between −0.3 and
0.3 V (vs Li+/Li).
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4

Homocoupling of 2-Phenyl-Indole Using Oxidized Activated Carbons

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All reactions with AC were carried out in a Teflon capped vial equipped with a magnetic stirring bar under O2 atmosphere. Reactions were monitored with thin layer chromatography (TLC) with SiO2 on aluminium coated plates. Mixtures of EtOAc and n‐hexane (from 1:4 to 1:1) were used as eluents. All oAC‐catalysts were prepared from the same batch (Lot. H2430) of AC (100 mesh) obtained from Fluka. The catalytic activity of oACs was tested with the homocoupling reaction of 2‐phenyl‐indole as a standard (Table S1) to control the possible batch variability. NMR yields were measured with a Bruker 500 spectrometer using 1,3,5‐trimethoxybenzene dissolved in [D6]DMSO in a sealed capillary as an external standard. The crude products were dissolved in a measured amount of solvent and analysed with proton spectra. All the other NMR spectra were recorded on Varian 300, Bruker 400, and Bruker 500 spectrometers. High resolution mass spectra (EI+) were measured with MS JEOL JMS‐700. Electrochemical tests were performed at room temperature using an Interface 1000 electrochemical workstation (Gamry Instruments). The set‐up cell used for the experiments was a three‐electrode system consisting of a platinum coil as the counter electrode, a Pt wire as pseudo‐reference electrode with Fc/Fc+ as an internal standard and a glassy carbon electrode as a working electrode.
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