1983
DOI: 10.1016/0022-3093(83)90417-9
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IR-spectral study of vanadate vitreous systems

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Cited by 194 publications
(88 citation statements)
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“…The infrared spectrum of the sample containing 0.5 tool % Fe203, heat treated for 0.5 h, the band at 1320 cm-1 is due to BO4 vibration [93. The band at 1000 cm -~ is due to the terminal V-O stretching modes [14,15], and indicates the formation of isolated bonds and the presence of the symmetric V20 4-and VO 3-groups [16,17]. The band at 860cm -1 is due to V-O-V stretching vibration [14,18], whilst that at 600 cm-1 is assigned to bending modes of the PO4 group [19].…”
Section: Resultsmentioning
confidence: 99%
“…The infrared spectrum of the sample containing 0.5 tool % Fe203, heat treated for 0.5 h, the band at 1320 cm-1 is due to BO4 vibration [93. The band at 1000 cm -~ is due to the terminal V-O stretching modes [14,15], and indicates the formation of isolated bonds and the presence of the symmetric V20 4-and VO 3-groups [16,17]. The band at 860cm -1 is due to V-O-V stretching vibration [14,18], whilst that at 600 cm-1 is assigned to bending modes of the PO4 group [19].…”
Section: Resultsmentioning
confidence: 99%
“…This is assigned to VO 4 3− stretching mode. Dimitriev et al [13] reported that the band at~1,000 cm −1 in Ag 2 O-V 2 O 5 glassy system is due to bonding of Ag + ions with the unbridged double-bonded oxygen.…”
Section: Methodsmentioning
confidence: 98%
“…The band at position 920 cm −1 is assigned to VO 3 terminal stretching of the pyrovanadate ions. The intensity and position of this band start increasing slightly with [20]. The band at 1,020 cm −1 is related to the vibrations of the non-bridging V=O of the VO 5 groups [21].…”
Section: Dscmentioning
confidence: 93%