Abstract
Long-term creep (i.e., deformation under sustained load) is a significant material response that needs to be accounted for in concrete structural design. However, the nature and origin of concrete creep remain poorly understood and controversial. Here, we propose that concrete creep at relative humidity ≥ 50%, but fixed moisture content (i.e., basic creep), arises from a dissolution-precipitation mechanism, active at nanoscale grain contacts, as has been extensively observed in a geological context, e.g., when rocks are exposed to sustained loads, in liquid-bearing environments. Based on micro-indentation and vertical scanning interferometry data and molecular dynamics simulations carried out on calcium-silicate-hydrate (C-S-H), the major binding phase in concrete, of different compositions, we show that creep rates are correlated with dissolution rates - an observation which suggests a dissolution-precipitation mechanism as being at the origin of concrete creep. C-S-H compositions featuring high resistance to dissolution, and, hence, creep are identified. Analyses of the atomic networks of such C-S-H compositions using topological constraint theory indicate that these compositions present limited relaxation modes on account of their optimally connected (i.e., constrained) atomic networks.
Recommended Citation
I. Pignatelli et al., "A Dissolution-Precipitation Mechanism is at the Origin of Concrete Creep in Moist Environments," Journal of Chemical Physics, vol. 145, no. 5, American Institute of Physics (AIP), Aug 2016.
The definitive version is available at https://doi.org/10.1063/1.4955429
Department(s)
Materials Science and Engineering
Keywords and Phrases
Calcium silicate hydrate; Concrete structural designs; Dissolution precipitations; Material response; Moist environment; Molecular dynamics simulations; Topological constraints; Vertical scanning interferometries
International Standard Serial Number (ISSN)
0021-9606
Document Type
Article - Journal
Document Version
Final Version
File Type
text
Language(s)
English
Rights
© 2016 American Institute of Physics (AIP), All rights reserved.
Publication Date
01 Aug 2016