The first anodic scanning gives two oxidation peaks that are stably centered at 0.78 and 1.33 V, resulting from the de-alloying reaction (reverse reaction of Eq. 4) and conversion reaction (reverse reaction of Eq. 3), respectively [15, 55].
The anodic peaks that are centered at 1.1, 1.4, and 1.9 V are related to the de-alloying reaction (reverse reaction of Eq. 2) and the formation of Sb2S3 (reverse reaction of Eq. 1) [15, 15].
By combining forward and reverse reaction rates, a significant gain in computational efficiency is achieved.
In a buffered media, both the forward and reverse reactions are pseudo-first order.
Sequence forward and reverse reactions were run on a 3100 automated Capillary DNA Sequencer (PE Applied Biosystems).
Both forward and reverse reactions were performed to verify results.
All carbon tracking reactions are broken into elementary forward and reverse reactions.
PfaE3 was found to be catalytically active in both forward and reverse reactions (Table 1).
The forward and reverse reactions were run on a Rapid Cycler Instrument 2 (Idoha Technology Inc).
To each reaction corresponds a reverse reaction.
In the discharge process, reverse reaction occurs.
