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The Raman data showed that the nanocomposite coatings started to oxidize at 800 °C as compared to TiN, which have been oxidized even at 500 °C.
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AuNPs employed in this study persist in their atomic status without being oxidized, even after they were aerosolized in air or heated at 500 °C.
Investigations by surface-enhanced infrared absorption spectroscopy (SEIRAS) simultaneously with electrochemical measurement clarify that, for formic acid oxidation, adsorbed CO is not oxidized even at 1.4 V due to the absence of water, and thus practically no current is produced.
It means that in air condition, the Co core nanoparticles were partially oxidized even at room temperature and then were gradually oxidized to Co3O4 with the temperature rising to 800°C.
Because MAsIII and DMAsIII are rapidly oxidized even at temperatures < 0°C (Del Razo et al. 2001; Gong et al. 2001), these studies probably underestimated the concentrations of these metabolites.
Although H2O2 detoxification enzymes, like GPxs, Prxs and catalase, are more abundantly expressed than proteins involved in the redox signaling [ 28], cysteine residues of the ubiquitously expressed Prxs are prone to be oxidized at even relatively low H2O2 levels [ 29– 31].
A separation of surface and subsurface/bulk oxidation of NiAlOx and Ni/γ-Al2O3, both of which are readily oxidized even under mild conditions, is only achievable at temperatures between 190 and 195 K.
In contrast, the neutral semiquinonediimine radicals are oxidized at the same or even a lower potential than the parent phenylenediamines.
A few samples were oxidized at several oxidation levels.
However, because of its active chemical property, NaHS can be easily oxidized, even spontaneously ignited in the open air.
The catalysts were oxidized at 773 K and reduced at 673 K prior to the experiment.
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