The buffer was deoxygenated by purging with dry nitrogen gas.
All buffers were deoxygenated by bubbling with argon gas for at least 30 mins.
For studies of the reductive half reaction, the solution in the second syringe contained NADPH where the buffer was deoxygenated with Ar or N2 via bubbling.
Buffered solutions were deoxygenated by vigorous sparging with nitrogen for at least 2 h.
All solutions were deoxygenated by bubbling with N2 before the tests, and all electrochemical measurements were carried out in a water bath at 25 ± 1 °C.
Similarly, in La0.7Sr0.3MnO3 thin films, the MR increased from 55 to 85% when the thin films were deoxygenated by annealing in a reducing atmosphere [20].
The samples were deoxygenated by bubbling nitrogen during 10 min, and the gelation was performed in the 1 × 1 cm2 square-shaped holders (4 cm3 of volume) at 60°C in a heat bath.
Vials were deoxygenated by bubbling nitrogen prior to P540 addition and then transferred into a Bactron II (Shell laboratories).
Solutions were deoxygenated by adding an amount of 100 μL of glucose oxidase solution (c = 10 mg/mL) to 5 mL of glucose solution.
Water was deoxygenated by boiling, purging with ultrahigh-purity (UHP) N2 and storing in a 98% N2, 2% H2 anaerobic chamber (Coy Labs; industrial grade chamber gases were deoxygenated using a Pd catalyst).
Nitrogen was deoxygenated by filtering the moisture and oxygen through silica gel and titanium chips at 1, 000°C.
