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Flavohemoglobin acts by either catalyzing an O2-dependent denitrosylase reaction converting NO to a nitrate ion or N2O, or an anoxic reductive reaction forming NO−.
This means that plants will encounter amino acids half as often as they encounter nitrate ions, but each encounter with an amino acid yields twice as many nitrogen atoms as an encounter with a nitrate ion.
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In the second step, a standard solution of lanthanum nitrate (0.1 mol L−1, confirmed by measurement with a nitrate ion-selective electrode) is added stepwise, forming LaF3 with the freed fluoride ions.
A free nitrate ion, NO3−, is the primary form of stored NOx on the potassium phase at all temperatures, but there was significant nitrite formation observed below 200 °C during short adsorption times.
A wide and strong band at 1,379 cm−1 strongly indicates that the nitrate ion is a counter ion.
Also, Hamoudi et al. (2007a) modified MCM-48 with ammonium groups and used as an adsorbent for removing nitrate ion from aqueous solution.
It was clearly shown with the three methods that an increase in the nitrate ion concentration activates the reduction of the Ag+ ions; the overvoltage of the reaction decreases markedly.
Thus in TlNO3 where the nitrate ion has an anion bonding strength of −0.11 vu, Tl+ behaves like Rb+, adopting an undistorted environment of nine Tl−O bonds of 0.11 vu each.
To protect against methemoglobinemia, the SDWA has established an MCL of 45 mg/L as nitrate ion (NO3) or 10 mg/L as nitrate-nitrogen in drinking water (U.S. EPA 2010a).
Depending on the reaction, this may be due to the Pb2+(aq) ion, which has a standard reduction potential (E0) of −0.125 V, or the nitrate ion, which under acidic conditions has an E0 of +0.956 V.
In compound 1, the nitrate ion is coordinated as a chelating ligand and essentially both the O atoms of the nitrate occupy one axial site.
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