Accelerated diffusion methods for inorganic-nitrogen analysis of soil extracts and water

被引:88
作者
Khan, SA [1 ]
Mulvaney, RL [1 ]
Mulvaney, CS [1 ]
机构
[1] UNIV ILLINOIS,DEPT NAT RESOURCES & ENVIRONM SCI,URBANA,IL 61801
关键词
D O I
10.2136/sssaj1997.03615995006100030032x
中图分类号
S15 [土壤学];
学科分类号
0903 ; 090301 ;
摘要
The major limitation of diffusion methods for N analysis is the time required to obtain the results - typically from one to several days. Methods were developed that involve a much shorter period for diffusion. In these methods, 10- to 100-mL samples of 2 or 4 M KCI soil extract or water were treated with MgO, or MgO plus Devarda's alloy, in a 473-mL (I-pint) wide-mouth Mason jar to liberate NH4-N, NO3-N, and/or NO2-N as NH3. The jar was placed on an electric griddle maintained at 45 to 50 degrees C. Gaseous NH3 was collected in 5 mt of H3BO3 indicator solution in a petri dish attached to the Mason jar lid, for quantitative determination by acidimetric titration. Complete recovery of 4 mg of N was achieved from 10 or 20 mt in 1.5 to 5 h. Recovery from 50 or 100 mt was complete in 5 to 8.5 h with 1 to 2 mg of N. The methods permit N-15 analysis of the diffused NH3-N. Isotopic analyses of labeled soil extracts were accurate to within 3%, as determined by isotope-dilution calculations. Diffusions from 10 to 50 mt were subject to very little, if any, interference from decomposition of alkali-labile organic-N compounds.
引用
收藏
页码:936 / 942
页数:7
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