<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ananthanarayanan, A.</style></author><author><style face="normal" font="default" size="100%">Ambashta, R. D.</style></author><author><style face="normal" font="default" size="100%">Sudarsan, V.</style></author><author><style face="normal" font="default" size="100%">Ajithkumar, T.</style></author><author><style face="normal" font="default" size="100%">Sen, D.</style></author><author><style face="normal" font="default" size="100%">Mazumder, S.</style></author><author><style face="normal" font="default" size="100%">Wattal, P. K.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Structure and short time degradation studies of sodium zirconium phosphate ceramics loaded with simulated fast breeder (FBR) waste</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Nuclear Materials</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">APR</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">487  </style></volume><pages><style face="normal" font="default" size="100%">5-12</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Sodium zirconium phosphate (NZP) ceramics have been prepared using conventional sintering and hot isostatic pressing (HIP) routes. The structure of NZP ceramics, prepared using the HIP route, has been compared with conventionally sintered NZP using a combination of X-ray diffraction (XRD) and (P-31 and Na-23) nuclear magnetic resonance (NMR) spectroscopy techniques. It is observed that NZP with no waste loading is aggressive toward the steel HIP -can during hot isostatic compaction and significant fraction of cations from the steel enter the ceramic material. Waste loaded NZP samples (10 wt% simulated FBR waste) show significantly low can -interaction and primary NZP phase is evident in this material. Upon exposure of can -interacted and waste loaded NZP to boiling water and steam, P-31 NMR does not detect any major modifications in the network structure. However, the Na-23 NMR spectra indicate migration of Na+ ions from the surface and possible re -crystallization. This is corroborated by Small -Angle Neutron Scattering (SANS) data and Scanning Electron Microscopy (SEM) measurements carried out on these samples.</style></abstract><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">2.447</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Nadol, Athulya</style></author><author><style face="normal" font="default" size="100%">Ajithkumar, T. G.</style></author><author><style face="normal" font="default" size="100%">Singla, Rashmi</style></author><author><style face="normal" font="default" size="100%">Alex, T. C.</style></author><author><style face="normal" font="default" size="100%">Kumar, Sanjay</style></author><author><style face="normal" font="default" size="100%">Bhatt, Himal</style></author><author><style face="normal" font="default" size="100%">Deo, M. N.</style></author><author><style face="normal" font="default" size="100%">Sen, Debasis</style></author><author><style face="normal" font="default" size="100%">Ambashta, R. D.</style></author><author><style face="normal" font="default" size="100%">Bajpai, R. K.</style></author><author><style face="normal" font="default" size="100%">Shivakumar, Y. C.</style></author><author><style face="normal" font="default" size="100%">Manohar, S.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Fly-ash-based geopolymers: leachability and solid-state NMR investigations</style></title><secondary-title><style face="normal" font="default" size="100%">Bulletin of Materials Science</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">aluminosilicate network</style></keyword><keyword><style  face="normal" font="default" size="100%">Fly ash</style></keyword><keyword><style  face="normal" font="default" size="100%">Geopolymers</style></keyword><keyword><style  face="normal" font="default" size="100%">leaching</style></keyword><keyword><style  face="normal" font="default" size="100%">Solid-state NMR</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2026</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAR</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">49</style></volume><pages><style face="normal" font="default" size="100%">54</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	This study aims to explore how leaching impacts the microstructure of a selected fly ash-derived geopolymer and evaluate its potential for near-surface disposal of radioactive waste. The uniqueness of this geopolymer formulation is its ability to form an aluminosilicate network that remains resistant to structural changes upon contact with water. The leach index of base elements such as Ca, Al, Na and Si was between 11 and 13, suggesting that the formulation is superior to Portland cement or conventional hydraulic cement. Solid-state NMR reveals that the water-interacted specimen has no contamination of the zeolite phase and all the Na is incorporated into the aluminosilicate geopolymer gel network, which also confirms that the glassy network of the geopolymer is responsible for imparting low leachability of base elements from its structure, and there is no labile sodium available for exchange as in zeolites.&lt;/p&gt;
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	Foreign&lt;/p&gt;
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	2.1&lt;/p&gt;
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