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The infrared spectra of two B type bands, ν2 and 2ν1, of 14N16O2 have been recorded under high resolution. Ground state combination differences from these bands have been combined with combination differences obtained in previous studies and eight pure rotational microwave transitions to yield improved ground state rotational constants. Upper state constants and band centers for the ν2 and 2ν1 bands are also reported. The 2ν1 band contains internal intensity anomalies believed to arise from a weak Coriolis interaction with the much stronger ν1 + ν3 band. Equilibrium rotational constants have been calculated. The equilibrium structure of the molecule is: rc = 1.1945 ± 0.0005 Å and Θc = 133.85 ± 0.10°. For the sake of comparison, effective, substitution, and average structures are also reported.

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The addition of gadolinium nitrate solution in the moderator of Hydro‐Québec's Gentilly 2 reactor led to an unexpected depletion of gadolinium (Gd) by precipitation. Analysis of moderator samples revealed that bicarbonate (HCO3−) was the main anionic impurity. A study of the complexing reactions of Gd in concentrated solutions (0.0509M) of Gd(NO3)3 showed that in the absence of HCO3− and at pH < 6, the species in equilibrium are distributed as follows: predominant: Gd3+, NO3− and [GdNO3]2+; and traces: [GdOH]2+ and [Gd(NO3)2]+. An increase in pH over 6.4 led to the formation of the solid phase: Gd2(OH)5.1(NO3)0.9. In the presence of bicarbonate, the solid phase Gd2(OH)5.0(NO3)1.0 is visually detected at a pH as low as 5.8. In other respects, analysis of dilute solutions (0.00065M) of Gd(NO3)3 containing bicarbonate allows the solid phase precipitating between pH 5.5 and 6.6 to be ascribed to the formula Gd2(OH)4CO3·3H2O. In the absence of HCO3−, no precipitation occurred up to pH 6.8. Finally, the loss of Gd from the moderator was established as being due to the formation of a hydroxide carbonate salt.