journal article·2005-04

Formation of metaphosphate hydrogels and their proton conductivities

Takafumi Akamatsu, Toshihiro Kasuga, Masayuki Nogami

Journal of Non-Crystalline Solids· Volume 351· Issue 8-9
Publisher page

Abstract

Abstract Fine-sized magnesium metaphosphate or calcium metaphosphate glass powders were reacted with water and hydration immediately occurred, resulting in the formation of hydrogels with high viscosity. 31P MAS-NMR spectra showed that the hydrogels contain orthophosphates and long-chain phosphates coordinated to H+ or M2+ (M = Mg, Ca) ions. The hydrogel derived from calcium metaphosphate glass (CP gel) contained a larger amount of orthophosphate group than that derived from magnesium metaphosphate glass (MP gel); the long-chain phosphates in the CP gel are easier to be broken by the hydration than those in the MP gel. No hydrogels were derived from barium metaphosphate or strontium metaphosphate glass powders. The hydrogel formation was suggested to be influenced by the bonding strength between the bivalent metal ions (M2+) and non-bridging oxygens in the phosphates. The CP gel and MP gel showed high electrical conductivities (e.g., 5 and 0.7 mS/cm, respectively, at 30 °C).The conductivities were suggested to originate from proton conduction due to coexistence with large amounts of acidic P–OH groups and water molecules. They were related to the proton amount in the hydrogel; the amount in the CP gel was suggested to be larger than that in the MP gel.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Glass properties and applications · Luminescence Properties of Advanced Materials · Layered Double Hydroxides Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (24)

Show source-provided references
1. Yamashita · Chem. Mater. · 1996 · 8 · 269710.1021/cm9602858 ↗
2. Kobayashi · J. Biomed. Mater. Res. · 2001 · 57 · 47710.1002/1097-4636(20011215)57:4<477::AID-JBM1193>3.0.CO;2-5 ↗
3. Nakamura · J. Biomed. Mater. Res. · 2001 · 61 · 59310.1002/jbm.10224 ↗
4. Yamashita · Mater. Sci. Forum · 2003 · 426–432 · 323710.4028/www.scientific.net/MSF.426-432.3237 ↗
5. Kasuga · Chem. Lett. · 2001 · 30 · 82010.1246/cl.2001.820 ↗
6. Kasuga · J. Ceram. Soc. Jpn. · 2004 · 112 · S800
7. Kasuga · Adv. Mater. · 2002 · 14 · 149010.1002/1521-4095(20021016)14:20<1490::AID-ADMA1490>3.0.CO;2-M ↗
8. Colomban · 1992 · 38
9. Tatsumisago · J. Am. Ceram. Soc. · 1989 · 72 · 48410.1111/j.1151-2916.1989.tb06159.x ↗
10. Abe · J. Electrochem. Soc. · 1996 · 143 · 14410.1149/1.1836399 ↗
11. Nogami · J. Electrochem. Soc. · 1997 · 144 · 217510.1149/1.1837760 ↗
12. Nogami · J. Am. Ceram. Soc. · 2001 · 84 · 255310.1111/j.1151-2916.2001.tb01052.x ↗
13. Nogami · J. Phys. Chem. B · 2001 · 105 · 465310.1021/jp010611t ↗
14. Tatsumisago · Solid State Ionics · 1992 · 50 · 17210.1016/0167-2738(92)90229-I ↗
15. Matsuda · J. Ceram. Soc. Jpn. · 2000 · 108 · 4510.2109/jcersj.108.45 ↗
16. Park · Trans. Mater. Res. Soc. Jpn. · 2001 · 26 · 71
17. Umegaki · Bull. Chem. Soc. Jpn. · 1975 · 48 · 145210.1246/bcsj.48.1452 ↗
18. Brow · J. Non-Cryst. Solids · 2000 · 263&264 · 110.1016/S0022-3093(99)00620-1 ↗
19. Lippmaa · J. Am. Chem. Soc. · 1980 · 102 · 488910.1021/ja00535a008 ↗
20. Bunker · J. Non-Cryst. Solids · 1984 · 64 · 29110.1016/0022-3093(84)90184-4 ↗
21. Minami · J. Am. Ceram. Soc. · 1977 · 60 · 23210.1111/j.1151-2916.1977.tb14113.x ↗
22. Montagne · J. Non-Cryst. Solids · 1998 · 223 · 4310.1016/S0022-3093(97)00444-4 ↗
23. Dietzel · Z. Electrochem. · 1942 · 48 · 9
24. Vogal · 1985 · 37