State Key Laboratory of Forest and Soil Ecology, Institute of Applied Ecology, Chinese Academy of Sciences , Shenyang, Liaoning 110164, China.
Anal Chem. 2014 Apr 15;86(8):3787-92. doi: 10.1021/ac403756u. Epub 2014 Apr 2.
We report a new chemical method to determine the (15)N natural abundance (δ(15)N) for ammonium (NH4(+)) in freshwater (e.g., precipitation) and soil KCl extract. This method is based on the isotopic analysis of nitrous oxide (N2O). Ammonium is initially oxidized to nitrite (NO2(-)) by hypobromite (BrO(-)) using previously established procedures. NO2(-) is then quantitatively converted into N2O by hydroxylamine (NH2OH) under strongly acid conditions. The produced N2O 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(15)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 (15)N/(14)N analysis of NH4(+): (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 NH4(+) 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., HN3) and/or the use of specialized denitrifying bacterial cultures which may be impractical for many laboratories.
我们报告了一种新的化学方法,用于测定淡水(如降水)和土壤 KCl 浸提液中铵(NH4(+))的(15)N 天然丰度(δ(15)N)。该方法基于一氧化二氮(N2O)的同位素分析。铵最初通过次溴酸盐(BrO(-))氧化为亚硝酸盐(NO2(-)),采用先前建立的程序。在强酸条件下,NO2(-)被羟胺(NH2OH)定量转化为 N2O。生成的 N2O 用商业上可获得的吹扫和低温捕集系统通过同位素质谱仪(PT-IRMS)进行分析。基于典型的 4 毫升分析规模,δ(15)N 测量的标准偏差小于 0.3‰,通常优于 0.1‰(3 到 5 个重复)。与以前的方法相比,该技术具有几个优点,并有可能成为 NH4(+)的(15)N/(14)N 分析的常规方法:(1)与涉及扩散或蒸馏的方法相比,准备程序大大简化,准备时间大大缩短,因为所有反应都在同一个小瓶中进行,并且不需要从溶液中分离 NH4(+);(2)更适合于包括低氮浓度在内的低体积样品,空白大小为 0.6 至 2 nmol;(3)消除了使用剧毒试剂(例如 HN3)和/或使用可能对许多实验室不切实际的专门脱氮细菌培养物的必要性。