2019
DOI: 10.1016/j.radphyschem.2019.03.014
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Does the gelation temperature or the sulfuric acid concentration influence the dosimetric properties of radiochromic PVA-GTA Xylenol Orange Fricke gels?

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Cited by 28 publications
(17 citation statements)
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“…PVA-GTA Fricke gels have an R 1 -dose sensitivity around 0.025 s −1 .Gy −1 , approximately double that of standard agarose Fricke gels independent of the temperature during irradiation [ 128 ]. The R 1 -dose sensitivity increases further with another factor of 3 after addition of xylenol orange [ 129 , 130 , 131 ]. No significant changes in the dose sensitivity or ion diffusion coefficient were found for xylenol orange PVA-GTA Fricke gels prepared at different gelation temperatures between 6 °C and 42 °C.…”
Section: Fricke Gel Dosimetersmentioning
confidence: 99%
“…PVA-GTA Fricke gels have an R 1 -dose sensitivity around 0.025 s −1 .Gy −1 , approximately double that of standard agarose Fricke gels independent of the temperature during irradiation [ 128 ]. The R 1 -dose sensitivity increases further with another factor of 3 after addition of xylenol orange [ 129 , 130 , 131 ]. No significant changes in the dose sensitivity or ion diffusion coefficient were found for xylenol orange PVA-GTA Fricke gels prepared at different gelation temperatures between 6 °C and 42 °C.…”
Section: Fricke Gel Dosimetersmentioning
confidence: 99%
“…One of the most relevant matrix modifications may be the crosslinking of polyvinyl alcohol with glutaraldehyde for Fricke-based dosimetry [ 119 ]; in this case, the main motivation was simplifying the gelling process of PVA by using a similar approach consistent with that used in glutaraldehyde and gelatin. Moreover, the influence of gelling temperature on this type of matrix was studied by Gallo et al [ 26 , 120 ]. An extensive and complete revision of these types of dosimeters can be found elsewhere [ 12 ].…”
Section: Chemical and Physical Interactions Present In Gel Dosimetrymentioning
confidence: 99%
“…Indeed, GTA-PVA gel is a well-known matrix able to mimic efficiently the physiological thermal properties of tissues [19]. The procedure used for the hydrogel preparation, described in detail elsewhere [20,21], is here briefly summarized. PVA-GTA hydrogel was prepared by mixing a PVA solution with a GTA solution.…”
Section: Phantomsmentioning
confidence: 99%