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A novel technique to determine organic processes in pig wastes
Author(s) -
Hobbs Philip J,
Johnson Richard,
Chadwick David
Publication year - 1999
Publication title -
journal of the science of food and agriculture
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 142
eISSN - 1097-0010
pISSN - 0022-5142
DOI - 10.1002/(sici)1097-0010(199902)79:2<199::aid-jsfa158>3.0.co;2-3
Subject(s) - acetic acid , chemistry , phenol , methanogenesis , methane , carbon dioxide , ammonia , decomposition , organic acid , organic matter , phenols , environmental chemistry , organic chemistry
Complex processes concerning declining concentration of organic matter within pig wastes have been investigated using deuterated phenol ( d 5 ) and acetic acid ( d 4 ) over a ten day period. Decomposition rates of products responsible for odours and pollution were also quantified. These products included the volatile fatty acids, phenols and indoles as well as gaseous methane and carbon dioxide. The last two were quantified in the headspace flow to assess methanogenesis and the activity of bacteria. The relative rates of emission, production and bio‐decay were calculated as exponential curves showing that acetic acid was lost through emission and bio‐decay with half lives of 158 h and 95 h, respectively. Bio‐production of acetic acid was very low. The emission rate of methane was 4.0 g m −3 d −1 . The ratio of methane generated to the bio‐decay of acetic acid concentration was 1: 66. The decline of acetic acid in slurry was shown to be a concentration‐dependent process. Other volatile fatty acids demonstrated similar declining concentration characteristics but at a lesser rate. This was also the case for 4‐methyl phenol with a half life of 495 h. However phenol demonstrated different declining concentration and production characteristics with a maximum concentration of 85 mg l −1 at 175 h. Carbon dioxide was produced at a greater rate than acetic acid was lost from the slurry (a ratio of 1.88: 1.0). Ammonia was emitted at a rate of 4.7 g m −2 d −1 . © 1999 Society of Chemical Industry