Chemical Method for Nitrogen Isotopic Analysis of
Ammonium at Natural Abundance
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Abstract
We report a new chemical method to
determine the <sup>15</sup>N
natural abundance (δ<sup>15</sup>N) for ammonium (NH<sub>4</sub><sup>+</sup>) in freshwater (e.g., precipitation) and soil KCl extract.
This method is based on the isotopic analysis of nitrous oxide (N<sub>2</sub>O). Ammonium is initially oxidized to nitrite (NO<sub>2</sub><sup>–</sup>) by hypobromite (BrO<sup>–</sup>) using
previously established procedures. NO<sub>2</sub><sup>–</sup> is then quantitatively converted into N<sub>2</sub>O by hydroxylamine
(NH<sub>2</sub>OH) under strongly acid conditions. The produced N<sub>2</sub>O is analyzed by a commercially available purge and cryogenic
trap system coupled to an isotope ratio mass spectrometer (PT-IRMS).
On the basis of a typical analysis size of 4 mL, the standard deviation
of δ<sup>15</sup>N measurements is less than 0.3‰ and
often better than 0.1‰ (3 to 5 replicates). Compared to previous
methods, the technique here has several advantages and the potential
to be used as a routine method for <sup>15</sup>N/<sup>14</sup>N analysis
of NH<sub>4</sub><sup>+</sup>: (1) substantially simplified preparation
procedures and reduced preparation time particularly compared to the
methods in which diffusion or distillation is involved since all reactions
occur in the same vial and separation of NH<sub>4</sub><sup>+</sup> from solution is not required; (2) more suitability for low volume
samples including those with low N concentration, having a blank size
of 0.6 to 2 nmol; (3) elimination of the use of extremely toxic reagents
(e.g., HN<sub>3</sub>) and/or the use of specialized denitrifying
bacterial cultures which may be impractical for many laboratories