Abstract:Glasses with composition (ZnO)30(MgO) x (P2O5)70−x (x = 5, 8, 10, 13, 15, 18, and 20 mol.%) have been successfully prepared by the melt-quenching technique. Degradation study has been carried out by means of measuring their chemical durability against buffer solutions with initial pH values of 4.01, 7.00, and 10.01 at an ambient temperature for up to 30 days. The dissolution rate (D R) was obtained by calculating the measured weight loss of the glasses per unit surface area per unit immersion time. The results… Show more
“…This is due to the expected strong ionic cross-linking in the phosphate network structure from the inclusion of Mg 2+ , Zn 2+ and Ca 2+ cations and their respective charge-to-size ratios (0.0232, 0.0227 and 0.0175). The network structure would then be more capable of suppressing the onset of crystallisation in line with previous results [ 20 , 33 , 36 , 37 ]. However, previous studies have also shown that increased network stability is associated with a higher T g due to the increased energy required to fracture the structural bonds that contradicts the comparatively low T g found in these results.…”
Section: Discussionsupporting
confidence: 89%
“…However, previous studies have also shown that increased network stability is associated with a higher T g due to the increased energy required to fracture the structural bonds that contradicts the comparatively low T g found in these results. However, this could be accounted for by the general decrease in T g found in ultraphosphate glasses compared to metaphosphate compositions as reported by Ahmed et al [ 12 , 20 , 34 , 37 ]. Based on previous metaphosphate glass compositions studied by Morikawa et al [ 34 ], the large PW may also be attributed to a mixed cation effect between the Mg 2+ and Ca 2+ ions.…”
Section: Discussionmentioning
confidence: 87%
“…Such compounds would correlate with the ionic constituents of the CorGlaes ® Pure 107 composition and have been previously reported to precipitate during PG dissolution [37, 63]. These phases are expected to form via hydrolysis mechanisms with the observed decrease in media pH over the immersion period resulting from the phosphoric acid (H 3 PO 4 ) dissolution by-product [37, 63]. However, the precise identification of each amorphous phase from the available FTIR/Raman spectra is restricted due to the similar IR signals of these salts and associated band overlapping.…”
A degradable ultraphosphate (55 mol % P2O5) quinternary phosphate glass composition has been characterised in terms of its chemical, mechanical and degradation properties both as a bulk material and after drawing into fibres. This glass formulation displayed a large processing window simplifying fibre drawing. The fibres displayed stiffness and strength of 65.5 ± 20.8 GPa and 426±143 MPa. While amorphous discs of the glass displayed a linear dissolution rate of 0.004 mg cm−2 h−1 at 37 °C, in a static solution with a reduction in media pH. Once drawn into fibres, the dissolution process dropped the pH to <2 in distilled water, phosphate buffer saline and corrected-simulated body fluid, displaying an autocatalytic effect with >90 % mass loss in 4 days, about seven times faster than anticipated for this solution rate. Only cell culture media was able to buffer the pH taking over a week for full fibre dissolution, however, still four times faster dissolution rate than as a bulk material. However, at early times the development of a HCA layer was seen indicating potential bioactivity. Thus, although initial analysis indicated potential orthopaedic implant applications, autocatalysis leads to accelerating degradation in vitro.
“…This is due to the expected strong ionic cross-linking in the phosphate network structure from the inclusion of Mg 2+ , Zn 2+ and Ca 2+ cations and their respective charge-to-size ratios (0.0232, 0.0227 and 0.0175). The network structure would then be more capable of suppressing the onset of crystallisation in line with previous results [ 20 , 33 , 36 , 37 ]. However, previous studies have also shown that increased network stability is associated with a higher T g due to the increased energy required to fracture the structural bonds that contradicts the comparatively low T g found in these results.…”
Section: Discussionsupporting
confidence: 89%
“…However, previous studies have also shown that increased network stability is associated with a higher T g due to the increased energy required to fracture the structural bonds that contradicts the comparatively low T g found in these results. However, this could be accounted for by the general decrease in T g found in ultraphosphate glasses compared to metaphosphate compositions as reported by Ahmed et al [ 12 , 20 , 34 , 37 ]. Based on previous metaphosphate glass compositions studied by Morikawa et al [ 34 ], the large PW may also be attributed to a mixed cation effect between the Mg 2+ and Ca 2+ ions.…”
Section: Discussionmentioning
confidence: 87%
“…Such compounds would correlate with the ionic constituents of the CorGlaes ® Pure 107 composition and have been previously reported to precipitate during PG dissolution [37, 63]. These phases are expected to form via hydrolysis mechanisms with the observed decrease in media pH over the immersion period resulting from the phosphoric acid (H 3 PO 4 ) dissolution by-product [37, 63]. However, the precise identification of each amorphous phase from the available FTIR/Raman spectra is restricted due to the similar IR signals of these salts and associated band overlapping.…”
A degradable ultraphosphate (55 mol % P2O5) quinternary phosphate glass composition has been characterised in terms of its chemical, mechanical and degradation properties both as a bulk material and after drawing into fibres. This glass formulation displayed a large processing window simplifying fibre drawing. The fibres displayed stiffness and strength of 65.5 ± 20.8 GPa and 426±143 MPa. While amorphous discs of the glass displayed a linear dissolution rate of 0.004 mg cm−2 h−1 at 37 °C, in a static solution with a reduction in media pH. Once drawn into fibres, the dissolution process dropped the pH to <2 in distilled water, phosphate buffer saline and corrected-simulated body fluid, displaying an autocatalytic effect with >90 % mass loss in 4 days, about seven times faster than anticipated for this solution rate. Only cell culture media was able to buffer the pH taking over a week for full fibre dissolution, however, still four times faster dissolution rate than as a bulk material. However, at early times the development of a HCA layer was seen indicating potential bioactivity. Thus, although initial analysis indicated potential orthopaedic implant applications, autocatalysis leads to accelerating degradation in vitro.
“…Franks et al 15) and Lee et al 18) reported that the dissolution rate of MgOCaO Na 2 OP 2 O 5 glasses within the metaphosphate region decreased with increasing the MgO content. Smith et al 20) and Khor et al 17) reported that the chemical durability of MgOZnOP 2 O 5 glasses in near the metaphospate region was improved by increasing the MgO content in the glasses. In our previous work, the chemical durability of CaOP 2 O 5 TiO 2 metaphosphate glasses improved with the addition of MgO, while that of the invert glasses decreased when CaO was substituted by MgO.…”
Magnesium phosphate glasses exhibit unusual properties and were classified as 'anomalous phosphate glasses', because magnesium is attributed to a variation of the oxygen coordination number from 6 to 4. Magnesium in phosphate glasses acts as an intermediate oxide and its role was determined, relating to the phosphate chain length. In the present work, MgOP 2 O 5 TiO 2 / Nb 2 O 5 glasses with Mg/P ratio between 1.00 and 1.36 were successfully prepared by a meltquenching method. Magnesium in the glasses worked as a network former to form POMg bonds, which are cross-linked short phosphate chains that improved the glass-forming ability. Intermediate oxides (i.e., TiO 2 and Nb 2 O 5 ) in the glasses also cross-linked short phosphate chains to form P OTi/Nb bonds. The chemical durability of the glasses decreased with an increase in the Mg/P ratio, because magnesium, which entered the phosphate network, weakened the glass network to induce hydrolysis. The dissolution rate of Ti 4+ and Nb 5+ ions showed a decreasing tendency with an increase in the Mg/P ratio. The surfaces of the glasses were considered to be covered with gel-like oxide layers containing titanium or niobium and phosphate.
“…However, the introduction of another divalent oxide as MgO has been shown to reduce corrosion rates in aqueous solutions on zinc phosphate glasses [9]. This behavior has been related to some reasons such as the formation of more chemically resistant P-O-Mg bond, or to the decrease of P 2 O 5 content or to the introduction of dual two divalent oxides which can form MO 4 groups and block the pathway for the progress of the process corrosion [10,11].…”
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