2000
DOI: 10.1590/s0103-50532000000200011
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Criterious preparation and characterization of earthworm-composts in view of animal waste recycling. Part I. Correlation between chemical, thermal and FTIR spectroscopic analyses of four humic acids from earthworm-composted animal manure

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Cited by 23 publications
(24 citation statements)
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References 17 publications
(24 reference statements)
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“…The RAHAr sample spectrum was simulated starting from the assumption that the experimental spectrum is a sum of the spectra of Cu-4O and Cu-4N complexes, where the Cu-4O complex is present in a larger concentration than the Cu-4N complex ( Figure 5). This hypothesis is corroborated by the attributions of ν as (OCO) bands of carboxylate groups interacting with metals at ~ 1645 cm -1 in the FTIR spectra presented in part I of this study 3 10 atoms in the equatorial plane of an axial symmetry were more evident in the experimental spectra than the same parameters values for Cu-4N complexes. This fact can be indicative of the higher concentration of Cu-4O than Cu-4N complexes in the samples as considered above.…”
Section: Epr Spectroscopysupporting
confidence: 80%
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“…The RAHAr sample spectrum was simulated starting from the assumption that the experimental spectrum is a sum of the spectra of Cu-4O and Cu-4N complexes, where the Cu-4O complex is present in a larger concentration than the Cu-4N complex ( Figure 5). This hypothesis is corroborated by the attributions of ν as (OCO) bands of carboxylate groups interacting with metals at ~ 1645 cm -1 in the FTIR spectra presented in part I of this study 3 10 atoms in the equatorial plane of an axial symmetry were more evident in the experimental spectra than the same parameters values for Cu-4N complexes. This fact can be indicative of the higher concentration of Cu-4O than Cu-4N complexes in the samples as considered above.…”
Section: Epr Spectroscopysupporting
confidence: 80%
“…The doublet at δ 6.59 was tentatively assigned to aromatic hydrogens or biphenolic groups, although resonance of aromatic hydrogens of rings substituted with ortho or para amine groups can also appear in this region. Other weaker signals in the δ 7.1 to 6.2 range, more abundant in the COHA 1 H-NMR spectrum, can be due to the resonance of pyrrolic or indolic type heterocyclic hydrogens, in agreement with the high nitrogen content of the samples 3 . The presence of pyrrolic hydrogens is in agreement with the existence of porphyrin structures, as suggested by the EPR parameters for the Fe 3+ and Cu 2+ 16.0 Hz), these signals can be assigned to the resonance of trans hydrogens of conjugated double bonds of groups like C(=O)R (R = alkyl, ether), present in the pyrrolic structure 36 .…”
Section: H Nmr Spectroscopysupporting
confidence: 54%
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