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Effects of decalcification on the microstructure and surface area of cement and tricalcium silicate pastes
Authors:Jeffrey J Thomas  Jeffrey J Chen  Andrew J Allen  Hamlin M Jennings  
Affiliation:

a Department of Civil and Environmental Engineering, Northwestern University, Evanston, IL 60208, USA

b Department of Materials Science and Engineering, Northwestern University, Evanston, IL 60208, USA

c Materials Science and Engineering Laboratory, National Institute of Standards and Technology, Gaithersburg, MD 20899, USA

Abstract:Thin coupons of white portland cement (WPC) and tricalcium silicate paste were decalcified by leaching in concentrated ammonium nitrate solutions, resulting in calcium-to-silicon molar ratios (C/S) ranging from 3.0 (control) down to 0.3. The microstructure and surface area were measured using both small-angle neutron scattering (SANS) and nitrogen gas sorption. The intensity in the SANS data regime corresponding to the volume fractal C-S-H gel phase increased significantly on leaching, and the total surface area per unit specimen volume measured by SANS doubled on leaching from C/S=3.0 to near C/S=1.0. The nitrogen BET surface area of the WPC pastes, expressed in the same units, increased on decalcification as well, although not as sharply. The primary cause of these changes is a transformation of the high-density “inner product” C-S-H gel, which normally has a low specific surface area as measured by SANS and nitrogen gas sorption, into a morphology with a high specific surface area. The volume fractal exponent corresponding to the C-S-H gel phase decreased with decalcification from 2.3 to 2.0, indicating that the equiaxed 5 nm C-S-H globule building blocks that form the volume fractal microstructure of normal, unleached cement paste are transformed by decalcification into sheetlike structures of increasing thickness.
Keywords:Calcium silicate hydrate (C-S-H)  Microstructure  Small-angle neutron scattering  Surface area  Degradation
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