4.6 Article

Phase Formation and Evolution in Mg(OH)2-Zeolite Cements

Journal

INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
Volume 57, Issue 6, Pages 2105-2113

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.7b04201

Keywords

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Funding

  1. Engineering and Physical Sciences Research Council (EPSRC) through the University of Sheffield/University of Manchester Doctoral Training Centre Nuclear FiRST [EP/G037140/1]
  2. Engineering and Physical Sciences Research Council (EPSRC) through Nuclear Decommissioning Authority CASE award
  3. EPSRC
  4. BBSRC
  5. University of Warwick
  6. Birmingham Science City Advanced Materials Projects by Advantage West Midlands (AWM) [1, 2]
  7. European Regional Development Fund (ERDF)
  8. Department of Energy and Climate Change

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The mineralogy and structure of cements in the system Mg(OH)(2)-NaAlO2-SiO2-H2O are investigated, with a view toward potential application in the immobilization of Mg(OH)(2)-rich Magnox sludges resulting from historic United Kingdom nuclear operations. The reaction process leading to the formation of these aluminosilicate binders is strongly exothermic, initially forming zeolite NaA (LTA structure), which is metastable in low SiO2/Al2O3 binders, slowly evolving into the more stable sodalite and faujasite framework types. Notable chemical reaction of Mg(OH)2 was only identified in the formulation with SiO2/Al2O3 = 1.3 (the lowest molar ratio among those tested) after extended curing times. In this case, some of the Mg(OH)(2) reacted to form an Mg Al OH layered double hydroxide. These results demonstrate that encapsulation of Magnox sludge waste streams could be carried out in these alternative binders but that the binders would encapsulate rather than chemically incorporate the Mg(OH)(2) into the wasteform unless low SiO2/Al2O3 ratios are used.

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