2001
DOI: 10.1039/b005666i
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Bone mineral: evidence for hydroxy groups by inelastic neutron scattering

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Cited by 54 publications
(53 citation statements)
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“…Hydroxyl bands disappeared in the spectrum of fluorine substituted HA, which is why some researchers have neglected the existence of hydroxyl groups for mineral bone, [53] while others subscribe to the view that in poor crystalline apatite, hydroxyl groups are simply not resolved. [54] The results of the present study indicate that there was enough coupling to the fluoride to mask the characteristic hydroxyl band. There is also no evidence of bands that could be attributed to the OH…..F…..HO groups in all spectra.…”
Section: E Fourier Transform Infrared Analysismentioning
confidence: 85%
“…Hydroxyl bands disappeared in the spectrum of fluorine substituted HA, which is why some researchers have neglected the existence of hydroxyl groups for mineral bone, [53] while others subscribe to the view that in poor crystalline apatite, hydroxyl groups are simply not resolved. [54] The results of the present study indicate that there was enough coupling to the fluoride to mask the characteristic hydroxyl band. There is also no evidence of bands that could be attributed to the OH…..F…..HO groups in all spectra.…”
Section: E Fourier Transform Infrared Analysismentioning
confidence: 85%
“…Por comparação direta entre o espectro infravermelho do material fóssil e o do padrão de fosfato de cálcio do SDBS, foi possível concluir que as bandas localizadas em torno de 600 e 1050 cm -1 são associadas a grupos atômicos comuns aos dois materiais. Em particular, estas bandas podem ser atribuídas a vibrações do grupo fosfato 9,10 . Já as bandas localizadas em torno de 3500 cm -1 no espectro do fóssil podem ser atribuídas a vibrações do grupo OH 10 , uma vez que o fosfato de cálcio hidróxido, Ca 5 (PO 4 ) 3 (OH), foi identificado, através da técni-ca de difração de raios-X, como uma fase cristalina secundária.…”
Section: Resultsunclassified
“…As shown in the FT-IR spectra in Fig. 3, the IR absorptions due to OH − and PO4 3− in a typical HAp structure 17,18) were observed in all of the HAp nanoparticles prepared under different conditions. In brief, the peaks at 3,573 and 632 cm −1 were attributed to O-H stretching vibrations in the HAp lattice, respectively, and the characteristic peaks due to PO 4 3− absorptions were found at 1092/1045 (ν3PO4 3− ), 963 (ν1PO4 3− ), 603/572 (ν4PO4 3− ), and 474 (ν2PO4 3− ) cm −1 .…”
Section: Preparation Of Hap Nanoparticlesmentioning
confidence: 89%