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Reactions of Ammonia and Urea Hydrolysis Products with Soil
Author(s) -
Kissel D. E.,
Cabrera M. L.,
Ferguson R. B.
Publication year - 1988
Publication title -
soil science society of america journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.836
H-Index - 168
eISSN - 1435-0661
pISSN - 0361-5995
DOI - 10.2136/sssaj1988.03615995005200060050x
Subject(s) - urea , ammonia volatilization from urea , chemistry , ammonia , hydrolysis , fertilizer , titration , soil ph , urease , inorganic chemistry , soil water , biochemistry , soil science , organic chemistry , environmental science
A quantitative description of pH changes in N fertilizer application zones is needed to predict the degree of NH 3 formation in the soil solution. In particular, the pH changes following surface application of urea determine in part the degree of NH 3 formation and possible loss by volatilization. The objectives of our study were to compare the rise in soil pH following addition of urea and NH 4 OH to soil, and evaluate the importance of inorganic C reactions to any differences in the rise in pH caused by the two respective N sources. Titration curves with urea or NH 4 OH as a base were used to determine differences in the patterns of pH change. Up to pH 8.2, soil pH was raised identically by NH 4 OH and urea that had been completely hydrolyzed. Above pH 8.2, urea was less effective than NH 4 OH in raising soil pH. The lower effectiveness of urea was due in part to the urea‐C not forming CO 2 but remaining as HCO − 3 and CO 2− 3 in the soil solution. Part of the CO 2− 3 precipitated as CaCO 3 when enough urea was added to raise soil pH to 8.8. At a lower application rate of urea, which resulted in a soil pH of 7.15, no CaCO 3 was detected. These results demonstrate the importance of inorganic C from urea hydrolysis in providing resistance to a pH increase above pH 8.2 in concentrated fertilizer application zones.