Current densities were calculated using the electrodes’ geometric area of 2 cm2. Linear sweep voltammograms were recorded in a 1 M NaOH solution and always deaerated by argon (Ar) for 20 min prior to measurements. HER polarization curves were recorded from the open circuit potential (OCP) to −0.42 V (vs. RHE) at a polarization rate of 10 mV·s−1. Polarization curves were recorded at several temperatures from 25 to 75 °C, and temperatures were set with a water jacket connected to a LAUDA Alpha RA 8 thermostat. Stability was studied by recording chronoamperometry (CA) curves for HER at a potential of −0.22 V (vs. RHE) for half an hour. All electrochemical measurements were performed with a Metrohm Autolab potentiostat (PGSTAT302, Utrecht, The Netherlands) using the Electrochemical Software (Nova 2.1.4).
Alpha ra 8
The Alpha RA 8 is a laboratory equipment designed for precise and reliable analysis. It functions as a high-performance analytical instrument, providing accurate and consistent measurements. The core purpose of the Alpha RA 8 is to facilitate scientific research and testing across various industries.
Lab products found in correlation
7 protocols using alpha ra 8
Electrochemical Characterization of NiMo/Ti Catalysts
Current densities were calculated using the electrodes’ geometric area of 2 cm2. Linear sweep voltammograms were recorded in a 1 M NaOH solution and always deaerated by argon (Ar) for 20 min prior to measurements. HER polarization curves were recorded from the open circuit potential (OCP) to −0.42 V (vs. RHE) at a polarization rate of 10 mV·s−1. Polarization curves were recorded at several temperatures from 25 to 75 °C, and temperatures were set with a water jacket connected to a LAUDA Alpha RA 8 thermostat. Stability was studied by recording chronoamperometry (CA) curves for HER at a potential of −0.22 V (vs. RHE) for half an hour. All electrochemical measurements were performed with a Metrohm Autolab potentiostat (PGSTAT302, Utrecht, The Netherlands) using the Electrochemical Software (Nova 2.1.4).
Ultrasonic Processing of Pomegranate Juice
Carbon Steel Corrosion in CO2 Environment
All tests in this study were conducted in a system consisting of three double-walled glass cells connected to a cooling system (Alpha RA8, Lauda, Lauda-Königshofen, Germany) to maintain the temperature at 278 K (5 °C). Each cell has 4 ports to purge the CO2 gas (purity > 99.995%, Linde AG, Germany) (50–60 mL/min) and to insert working, counter, and Ag/AgCl reference electrodes. In the case of exposure test, the coupon was hanged on the Teflon wire, while in the electrochemical test, the coupons were weld to a stick made of high-alloyed material. Before each test, 500 mL condensate was used and purged strongly with Ar (purity > 99.998%, Linde) for 30 min, then 1 h with CO2 to reach the saturation state and stable pH (≈1.9).
Time-resolved Transient Absorption Spectroscopy
Specific Conductance Measurement Protocol
Freezing and Melting Dynamics of Ice
Fluorescent Compound Analysis via HPLC
HPLC was carried out on an Agilent 1200 liquid chromatograph (Agilent Technologies, Waldbronn, Germany) equipped with a quaternary pump operating at 0.7 mL min À 1 and a fluorescence detector irradiating at 225 nm and measuring at 306 nm.
A Rheodyne injector with a 20.0 μL loop was employed to spread the sample onto a Poroshell 120 EC C18 column (2.7 μm average particle size, 100 mm  4.6 mm i.d.).
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