Zhang Lin, Altabet Mark A, Wu Taixing, Hadas Ora
School for Marine Science and Technology, University of Massachusetts Dartmouth, New Bedford, Massachusetts 02744, USA.
Anal Chem. 2007 Jul 15;79(14):5297-303. doi: 10.1021/ac070106d. Epub 2007 Jun 14.
We report a new method for determining the 15N/14N of NH4+ at natural abundance level in both freshwater and seawater. NH4+ is first quantitatively oxidized to NO2- by hypobromite (BrO-) at pH approximately 12. After the addition of sodium arsenite to consume excess BrO-, yield is verified by colorimetric NO2- determination. NO2- is further reduced to N2O using a 1:1 sodium azide and acetic acid buffer solution using previously established procedures. The product N2O is then analyzed for isotopic composition using a continuous flow purge and cryogenic trap system coupled to an isotope ratio mass spectrometer. Reliable delta 15N values (standard deviation is 0.3 per thousand or better) are obtained over an NH4+ concentration range of 0.5-10 microM using 20 mL volumes of either freshwater or seawater samples. Higher concentration samples are readily diluted to lower concentration. Preexisting NO2- is removed by treatment with sulfanilic acid. There is no interference from any of the nitrogen-containing compounds tested except short-chain aliphatic amino acids (i.e., glycine) which typically are present at very low environmental concentrations. As compared to published methods, our approach is more robust, readily applicable at low concentrations and small sample volumes, and requires less time for preparation and analysis.
我们报告了一种在淡水和海水中测定天然丰度水平下NH₄⁺的¹⁵N/¹⁴N的新方法。NH₄⁺首先在pH约为12的条件下被次溴酸盐(BrO⁻)定量氧化为NO₂⁻。加入亚砷酸钠以消耗过量的BrO⁻后,通过比色法测定NO₂⁻来验证产率。使用先前建立的程序,用1:1的叠氮化钠和乙酸缓冲溶液将NO₂⁻进一步还原为N₂O。然后使用与同位素比率质谱仪联用的连续流动吹扫和低温捕集系统分析产物N₂O的同位素组成。使用20 mL体积的淡水或海水样品,在0.5 - 10 microM的NH₄⁺浓度范围内可获得可靠的δ¹⁵N值(标准偏差为千分之0.3或更好)。较高浓度的样品可轻松稀释至较低浓度。通过用磺胺酸处理可去除预先存在的NO₂⁻。除了短链脂肪族氨基酸(即甘氨酸)外,所测试的任何含氮化合物均无干扰,而短链脂肪族氨基酸在环境中的浓度通常非常低。与已发表的方法相比,我们的方法更稳健,易于应用于低浓度和小体积样品,并且制备和分析所需时间更少。