The time-dependent response of structural materials dominates our aging infrastructure’s life expectancy and has important resilience implications. For calcium-silicate-hydrates, the glue of cement, nanoscale mechanisms underlying time-dependent phenomena are complex and remain poorly understood. This complexity originates in part from the inherent difficulty in studying nanoscale longtime phenomena in atomistic simulations. Herein, we propose a three-staged incremental stress-marching technique to overcome such limitations. The first stage unravels a stretched exponential relaxation, which is ubiquitous in glassy systems. When fully relaxed, the material behaves viscoelastically upon further loading, which is described by the standard solid model. By progressively increasing the interlayer water, the time-dependent response of calcium-silicate-hydrates exhibits a transition from viscoelastic to logarithmic creep. These findings bridge the gap between atomistic simulations and nanomechanical experimental measurements and pave the way for the design of reduced aging construction materials and other disordered systems such as metallic and oxide glasses.
Like most engineering materials, concrete exhibits a time-dependent response, e.g. creep, when subjected to sustained external or internal load. This type of deformation not only impacts the life expectancy of our aging concrete infrastructure and the associated environmental footprint incurred for its rehabilitation, but also has important resilience implications. Although dislocation1 and shear transformation zones2,3 are at the heart of creep in crystalline materials and metallic glasses, the nanoscale mechanisms underlying time-dependent deformation in cementitious materials are complex and still the subject of intensive fundamental research4,5,6,7. For calcium-silicate-hydrates (C-S-H), the main binding phase in cementitious materials, this complexity can in parts be attributed to the presence of nanoconfined water, the material’s layered structure at the nanoscale8,9,10, its globular texture at the mesoscale11 and its multiscale porous structure12,13. These complexities further hinder the inherent difficulty in studying nanoscale longtime phenomena that arise from 18 orders of magnitude difference between characteristic time scales in atomic vibrations and creep deformation.
The majority of the literature focuses on continuum14,15, micromechanics16, and coupled microstructure-continuum models17 to predict creep in cementitious materials. Currently, a few phenomenological models are available that are calibrated with the goal of predicting a comprehensive database of experimental results18,19. These phenomenological models are critical in predicting long-term deformation of concrete structures, yet their link to fundamental materials physics remains to be understood. Also, the measurement of creep deformation in cementitious materials is further complicated owing to coexistence of long-term hydration process20 and the accompanying shrinkage deformation. The portion of creep deformation that is not owing to the hydration process, i.e., nonaging creep, constitutes a significant part of concrete’s overall time-dependent deformation and is the subject of this study. In an effort to address nonaging creep in C-S-H, microprestress solidification theory proposes the existence of frozen eigenstresses4 that relax over time following a power/logarithmic ε−t relation. Yet, the origins of C-S-H’s creep and its link to chemical composition and molecular structure of C-S-H cannot be explained by such phenomenological models and remain vastly unexplored. This calls for a molecular-level investigation of mechanisms behind C-S-H time-dependent phenomena.
Molecular dynamics (MD) simulation is the standard approach to explore atomic level processes that occur at the nanoscale. The first challenge in modeling cementitious materials is constructing an initial atomic structure for simulation purposes. Many studies have concluded that a structurally imperfect Tobermorite is a satisfactory model for C-S-H 9,21,22, which is the strategy adopted in the current paper. The next challenge is deriving accurate interatomic interactions such that reasonable agreement with a wide range of experimental observations is obtained from simulations. Several empirical force fields have been applied or developed for modeling C-S-H such as ClayFF23, CSH-FF24, CementFF25, and ReaxFF26. For details, the interested reader is referred to a recent comparative review on the subject27. Each of these force fields have their strengths and limitations. As elastic properties were included when parametrizing CSH-FF, it seems to be more suitable where mechanical properties are the focus of the study and hence it is the force field chosen for the current study. Availability of structures and force fields has spurred research in the cement and concrete community in areas such as free-energy calculations28, heat and mass transport properties29,30,31, polymer/C-S-H composites32, to just name a few.
Despite significant advances, with currently available technology, MD simulations remain constrained to small time scales on the order of microseconds33. As time-dependent phenomena such as creep occur on a time scale of hours, days and even years, a conventional MD simulation proves insufficient. From a probabilistic perspective, a phenomenon such as creep that occurs at longtime scales, can be viewed as a rare event process, the procession of a series of rare events34. In a non-equilibrium dynamic system such as a viscoelastic material under shear, the majority of the simulation time will be spent in a metastable basin. A jump to a more favorable basin by thermal activation would mean crossing an energy barrier, which requires a fluctuation with a low probability. This turns out to be the underlying cause of the disconnect between the macroscopic and nanoscopic time scales35. Biased molecular simulations, e.g., hyperdynamics36, metadynamics37, and Autonomous Basin Climbing35, are among the most noticeable time acceleration techniques. These approaches are limited to problems with small numbers of collective variables and fail for systems with soft modes. This makes their application to C-S-H rather irrelevant owing to the presence of many soft degrees of freedom in nanoconfined water molecules.
Inspired by experimental procedures in characterizing fatigue38 and the compaction observed in granular media due to mechanical disturbance39, to explore time-dependent behavior of C-S-H, we propose a simulation scheme based on the early work of Lacks and Osborne40. They applied incrementally increasing shear strain on a binary Lennard–Jones glass and subsequently unloaded the system after reaching a certain strain value. They observed that if the strain limit is small, the system undergoes aging and the internal energy decreases. A single cycle takes the system to a more favorable local minimum in the energy landscape. This approach artificially accelerates thermal fluctuation induced aging phenomenon. If several of these cycles are successively exerted on the sample, the system progressively visits lower minima same as those visited during a phenomenon such as creep.
In this paper, an incremental stress-marching technique is utilized to study time-dependent behavior of C-S-H. First, the C-S-H sample is loaded by cyclic perturbations where a relaxation behavior is observed. Subsequently, unloading and reloading of the sample takes place were a viscoelastic behavior is observed. The simulations show that this simple approach is able to explore different time-dependent regimes of deformation in C-S-H, ranging from creep relaxation to viscoelastic deformation. We finally investigate the impact of water content on the time-dependent behavior of C-S-H and establish its relation to the experimentally observed logarithmic creep.
Exploring shear stress–strain relationship in C-S-H
To study time-dependent phenomenon, we create a representative structure of C-S-H. The details on constructing a realistic C-S-H model can be found in the Methods section, Supplementary Note 1 and Supplementary Figs. 1–3. The stress–strain behavior of our C-S-H models in shear return a value of 21.1 ± 2.1 GPa for the shear modulus, which compares well with a value of 21 GPa reported elsewhere41. Particular features are noticeable in C-S-H’s stress–strain behavior (Supplementary Figs. 4–5). First, at strains smaller than 6.5%, the shear stress–strain curve is jagged, while exhibiting a linear behavior on average. This jagged response is indicative of a rippled energy landscape with numerous local minima42. Upon unloading from these local minima, a small yet non-negligible residual strain appears that is in the order of 0.1%. This is indeed similar to Lacks and Osborn’s observations in binary Lennard–Jones systems40. Second, C-S-H exhibits a sudden increase in the residual strain in the order of 2%, if loaded beyond 1.5 GPa, which can be viewed as the yield limit. To guarantee that incremental stress marching technique (ISM) explores time-dependent phenomena rather than the failure process, we ensure that the shear stress level at all times remains below the yield limit, τ + Δτ < τ f (see Supplementary Fig. 6 for a sensitivity analysis).
Cyclic loading and unloading of the models in stages I and II
A complex system such as C-S-H has a rugged energy landscape40,43 and the core objective of the incremental stress marching technique (see Methods section for details) is to facilitate the evolution of the system to the low-lying minima from its current state using gradient-based energy optimization as shown in Fig. 1a. Supplementary Note 2 and Supplementary Figs. 7–10 should be consulted for a simplified demonstration that the stress marching technique is equivalent to an inaccessibly long MD simulation. We subject the molecular structure of C-S-H, prepared as described in the methods section, to cyclic loading with different mean stress levels (stage I in Fig. 1b, also see Supplementary Fig. 11). As shown in Fig. 2a, this causes the structure to experience an incremental increase in shear strain, whereas the energy of the system drops to an asymptotic value in a matter of roughly 1000 stress cycles. We observe that the decline in internal energy occurs even when the mean stress level is zero. Similar behavior is observed for axial stress perturbations (Supplementary Fig. 12). To understand this behavior, we note that metastability is a characteristic of non-equilibrium systems such as C-S-H at the nanoscale. Using energy optimization, we merely obtain a structure whose energy is at a “local” minimum. However, owing to the metastable nature of C-S-H, the system is still far from the metabasin’s minimum in the energy landscape. Reaching this low-lying minimum requires overcoming a series of large energy barriers (hence, a very long simulation time). The main objective of ISM is providing a way to reach such favorable minima by a technique other than MD. Hence, each cycle of ISM, pushes the system over an energy barrier and into a new local minimum, which is more favorable than the previous one and hence lower in energy. This clearly indicates that we can view stage I as creep relaxation in shear. We note that the strain values observed here are larger than what is measured in macroscopic experiments44. This is due to the fact that the shear is applied parallel to the interlayer spacing and the layers can slide over each other with reduced restriction. However, in mesoscopic length scales such free movements are limited by an interconnected network of C-S-H layers. A realistic mesoscopic model would be needed to investigate such effects.
The Kohlrausch–Williams–Watts relaxation function has been extensively used as a phenomenological model to predict relaxation behavior in glass systems45,46. This function can be derived by several models such as hierarchically constrained dynamics47 or diffusion-trap45 and exhibits a stretched exponential shear strain as a function of cycles:
where N is the number of cycles overtook, N0 can be thought of as a characteristic relaxation number, β is the stretching exponent and γ is the engineering shear strain. We find that this function is capable of accurately fitting our data. We also note that the Normalized Root Mean Squared Error (NRMSE) values lie in the interval (0.02, 0.16) for all the fitted curves in this paper. This stretched exponential relation was also proposed when modeling glass relaxation by infliction of axial tapping cyclic stress perturbations48.
After reaching an asymptotic value of strain and energy in the first stage, we begin stage II by unloading the system and continuing the sequence of stress perturbations. We observe that in the course of the second stage, regardless of the stress history (the mean stress applied during the first stage) all systems reach a common value of energy minimum after 5000 cycles (Fig. 2b). As we are continuously relaxing box dimensions in our structural optimizations, it is in fact the enthalpy of the system that is minimized. The decreasing trend observed for all cases in Fig. 2c corroborates this assertion. The distinction between enthalpy and potential energy evolution proves more interesting for the third stage as described in the next section.
The results in Fig. 2a–b, can be understood in an enthalpy landscape framework, similar to the approach adopted to explain protein folding in biological systems49. A rugged enthalpy landscape can be envisioned for the system as seen by the schematic inset in Fig. 2b. Initially, the system resides in a metastable state, which is separated from the minimum of the basin by numerous small barriers. Application of external stress distorts the enthalpy landscape of the system and lowers the secondary barriers in the basin that would ultimately translate to higher transition rates50. Malandro and Lacks also showed that application of external shear strain causes the local minima of the potential energy surface to disappear, leading to mechanical instabilities that force the system into unexplored regions of the energy landscape. As seen from the inset of Fig. 2b, the landscape is transformed again upon unloading and the system is no longer in the minimum of the metabasin. Further cycling will again result in a drop in the internal energy to the lowest lying point in the metabasin, as observed in the inset.
To further understand the kinematic sources of relaxation in the C-S-H sample, Voronoi volume and the asphericity of the Voronoi cells were investigated for each atom. Asphericity is defined as the radius of the sphere with the same volume as the atom’s Voronoi cell51:
where A is the total area of the convex hull of the Voronoi cell and V is the Voronoi volume of the cell. At this stage, we distinguish between atoms in the defective intralayer calcium–silicate sheets and those forming the interlayer spacing. We observe a significant decrease in both the average asphericity and Voronoi volume of the interlayer constituents, interlayer calcium, hydroxide, and water molecules, whereas the values for the intralayer atoms remain constant (Fig. 2d). This can be regarded as evidence that the interlayer species are the main contributors to the time-dependent relaxation of C-S-H globules under constant stress.
Cyclic reloading of the models in stage III
If external stress is applied to the system at the end of the unloading stage, an instant increase in energy and shear strain is observed. Moreover, continued cyclic perturbations will cause the energy and strain of the system to further increase as shown in Fig. 3a–b. This form of cycle-dependent behavior is akin to that of viscoelastic behavior of solid materials. We verify that the final asymptotic strain scales linearly with the applied stress, see inset of Fig. 3a. Consequently, we use the phenomenological standard solid model to fit our data. This model, as shown in the inset of Fig. 3, is composed of two spring elements and a damper. Solving the differential equation governing this model under constant stress, τ0, leads to:
where G2 and G1 are the instantaneous stiffness and damping stiffness of the elastic components, λ = G2/μ0, and μ0 is proportional to the viscosity of the material. We obtain a value of G = 28.8 ± 1.3 GPa for the average of the resultant shear modulus. Although this has the same order of magnitude as those calculated in direct shear (21.1 ± 2.1 GPa), the discrepancy is non-negligible. This can in part be attributed to the approximate linear relationship that is assumed between time and number of cycles.
To further understand the observed viscoelastic phenomenon, rugged enthalpy and energy landscapes can be imagined for this complex system (inset of Fig. 3c). As the specimen is loaded, the system is seen climbing from the minimum of the basin to higher levels of potential energy. If we load a standard solid, we will observe the same behavior. This might seem counter-intuitive; however, a glance at the evolution of the system enthalpy (Fig. 3c) shows a decrease as stress perturbations continue. This means that with each cycle the system is moving to a more favorable minimum in the enthalpy landscape. Viscoelasticity also asserts that the system should recover the initial configuration and energy without any residual deformation. This is proven to be the case for C-S-H, as we note that in Fig. 3d the final energy state in stage I coincides with the final energy state in stage III.
Intraglobular to interglobar transition
The exponential viscoelastic behavior observed so far differs from the logarithmic creep observed in nanoindentation experiments carried out by Vandamme and Ulm52, where nanogranular behavior of C-S-H is cited as the origin of creep. According to nanogranular theory, C-S-H mesotxture can be viewed as the assembly of colloidal C-S-H nanoparticles of imperfect tobermorite-like minerals11. This theory was hypothesized on the basis of observations obtained from small angle X-ray and Neutron scattering as well as statistical nanoindentation experiments53,54,55. A simultaneous look at the experimental results and those obtained by atomistic simulations for models with different water content, raises the question: is creep caused by sliding of calcium–silicate layers over each other as envisioned by the Feldman–Sereda model10 or by the nanoglobular mesoscopic behavior. To address this question, we try to reproduce the sliding of C-S-H layers by investigating samples with different water content in the interlayer. In fact, inter and intraglobular behavior of C-S-H can be potentially explored by merely adjusting the number of interlayer water molecules as shown by the atomistic simulation boxes in Fig. 4a. Note that in the current study, intraglobular water and interlayer water denote the same constituents and can be used interchangeably. Here, we choose seven samples with varying water-to-silicon molar ratio (H/S), Fig. 4b. These samples are prepared simply by introducing more water molecules in the interlayers of the C-S-H model used for previous sections. We find that although the interlayer spacing increased linearly with water content, the density decreases linearly with it. We also investigate the behavior of amorphous ice, the structure of which can be obtained by quenching a thermal simulation box of water using structural optimization (infinitely fast). The amorphous ice sample can be regarded as the limiting case for the C-S-H water content (H/S → ∞).
We first fully relax these eight models by subjecting them to 104 stress cycles and subsequently reload them to monitor their behavior during stage III (Fig. 5a). For samples with low-water content, a purely exponential viscoelastic behavior is observed. However, as the water content increases, a logarithmic non-asymptotic component emerges. These results show a transition from a purely exponential viscoelastic behavior to a mixed exponential-logarithmic one. To capture this behavior quantitatively, we propose the following phenomenological function for samples with higher water content:
where 1/C and N0 are, respectively, creep compliance and characteristic number of stress perturbations. The exponential part of this equation is inspired by Eq. (3) and the logarithmic part can be interpreted according to experimental observations in nanoindentation tests52. The direct measurement of H/S at the mesoscale proves difficult. Here, we estimate H/S for experimental data based on the reported packing fraction, η, as follows:
where ρw and ρC-S-H are, respectively, the density of water and C-S-H. msim is the mass of the simulation box in g.mol−1, nSi-sim is the number of silicon atoms in the simulation box, and M w denotes the molecular weight of water in g.mol−1. We find that creep compliance measured for low and high density C-S-H in nanoindentation experiments is close to calculations from our atomistic simulations, Fig. 5b. The transition of behavior from purely exponential to a combined logarithmic-exponential brings us to the conclusion that each individual globule behaves viscoelastically. However, their sliding over each other, which is modeled by a larger separation of layers with interglobular water, introduces a logarithmic behavior. In other words, these results confirm the hypothesis that creep of hydrated cement originates from reconfiguration of C-S-H globules at the mesoscale rather than sliding of individual C-S-H sheets over each other.
To get a better understanding of the underlying cause of the transition of behavior from exponential to logarithmic, deformation profiles are plotted in Fig. 5c–d for specimens with different water content at several stages during the cycling process. It can be clearly observed that for the case with higher water content (H/S > 1.7), the layers can easily slide over each other and there is a negligible shear deformation in the solid part of the C-S-H layer and the deformation only arises from the interlayer constituents. For the case with lower water content (H/S < 1.7), a frictional interlocking exists between the motifs of the layers and larger energy barriers should be overcome for sliding to happen. This observation is in agreement with a decreasing trend observed previously for elastic constants as a function of H/S56. The energy barriers and their dependence on the interlayer spacing have been recently studied by Masoumi et al.57. Coordinate files for the initial structure before loading and after loading can be viewed as Supplementary Data 1 and 2, respectively. These data are for the case H/S ≈ 1.7.
In this paper, stress-induced time-dependent behavior of C-S-H was investigated by application of a chain of aging shear cycles at the nanoscale. We showed that if a C-S-H atomistic model is subjected to repeated aging/rejuvenation cycles under a constant shear stress, the potential energy of the system will decrease until an asymptotic value is reached. This is akin to relaxation in glassy systems and can be explained using stretched exponential hierarchically constrained dynamics model. Voronoi and asphericity analysis of the model during relaxation show that shear relaxation of C-S-H is rooted in reconfiguration of interlayer constituents. In addition, reloading the specimen after the relaxation stage will result in an increase in the potential energy of the system. We show that in spite of this increase, enthalpy still decreases, which means the system is moving to more favorable minima in the enthalpy landscape. We also demonstrate that this stage can be well described by a three-component standard solid model, akin to an exponential viscoelastic behavior. We observe a transition window, where the behavior changes from purely exponential to combined logarithmic-exponential behavior with increasing interlayer water content. A combined logarithmic-exponential function was also proposed for a phenomenological description of the observations. An in-depth analysis of shear deformation at the atomic level demonstrated the effectiveness of the shear locking mechanism as a potential venue to restrain non-asymptotic time-dependent behavior.
Despite the abovementioned striking observations using a rather simple approach, this work can benefit in many ways from future research at the intersection of cement and concrete science, molecular simulation, and statistical physics. Considering the complexity in modeling cementitious materials, we note that using a non-reactive classical force field limits our simulations to nonaging creep. Investigation of aging creep, i.e., creep associated with chemical reactions58 (breakage and formation of covalent bonds and deformation induced dissolution–precipitation mechanisms), can be conducted using a reactive potential in conjunction with the ISM. This could be computationally prohibitive, owing to the large number of enthalpy optimizations and the associated cost of employing reactive potentials. This motivates further research toward devising algorithms to reduce the cost of reaching a low-lying minimum. Furthermore, to truly test the observed intraglobular to interglobular transition behavior, prohibitively large atomistic models would be needed. This calls for realistic upscaling of C-S-H atomistic models through proper coarse-graining techniques and applying ISM to the model at the larger length scale. Regarding composition of C-S-H, one expects fewer bridging silicate tetrahedra to be present at higher calcium to silicon ratios (C/S). This means that the barriers owing to steric repulsion will be altered significantly and time-dependent behavior could possibly be affected. Moreover, previous research has shown that the number of hydrogen bonds increases with C/S, which alters the interlayer hydrogen bond network31. A separate study should be carried out to unravel the role played by composition.
From statistical physics standpoint, presence of small energy barriers59 in a complex system such as C-S-H limits the applicability of existing accelerated dynamics techniques. A future progress in this field can potentially unlock the true dynamic trajectory of long-term time-dependent response of structural materials. Assuming that the transition state theory is applicable for studying C-S-H time-dependent behavior60, the height of barriers separating two inherent structures, i.e., local minima, governs transition rates. Measuring the energy barriers for C-S-H, using methods such as Nudged Elastic Band61, proves futile due to the presence of many soft modes in nanoconfined water. This means that establishing a link between time and number of cycles in ISM would only be qualitative at best. Supplementary Note 2 and Supplementary Figs. 7–10 discuss a derivation using a simplified 1D synthetic energy landscape. However, similar results can be obtained more rigorously using higher dimensional SELs such as NK or transition matrix models62.
Altogether, the results of this work shed more light on various aspects of fundamental mechanisms that cause time-dependent behavior in C-S-H. Furthermore, acceleration techniques such as the proposed ISM would bridge the existing gap between time scales in atomistic simulations and nanomechanical testing of condensed phases, which would ultimately pave the way for rational design of construction materials, and other glassy systems such as oxide and metallic glasses with reduced aging characteristics.
C-S-H, the hydration product that is responsible for cement’s strength and durability, is a quasi-glassy material with an average C/S around 1.78,63. In this paper, we use a slightly modified version of the model proposed by Abdolhosseini Qomi et al.64, as it closely captures several key experimental observations such as density, basal spacing and XRD patterns (Supplementary Fig. 2)54,64,65. Similar atomic models of C-S-H can be constructed by following different procedures as carried out, for instance by Kumar et al.66 or Kovačević et al.67. For more simulation details, Supplementary Note 1 and Supplementary Figs. 1–3 should be consulted. Herein, the atomic structure of C-S-H is rationalized through structural modifications of Hamid’s 11 Å tobermorite68, a crystalline mineral with a layered structure composed of infinite dreierketten silicate chains with C/S = 1. To construct realistic molecular models of C-S-H akin to those observed in modern hydrated Portland cement, we randomly remove bridging and (occasionally) pairing sites from tobermorite’s infinite silicate chains. This method of constructing the molecular structure of C-S-H is shown to provide models that are in close agreements with 29Si NMR69, Inelastic Neutron Scattering54,70, normal and high-pressure X-Ray diffraction measurements55. The final composition reached is Ca1.7Si1.0O2.5(OH)1.7(H2O)0.9. Note that to study intraglobular to interglobular behavior, the amount of water in this formula is varied to observe different regimes of time-dependent behavior. The literature can be consulted for further detail on model construction9,64,65.
Force field and simulation details
Here, we use transferable CSH-FF potential24 designed particularly for cement hydrates. This ClayFF-based force field23 is shown to reproduce characteristics of C-S-H ranging from mechanical to thermal properties30,31. ReaxFF (a bond-order based potential) is an alternative force field for cementitious materials that possesses the ability to capture bond breakage/froming during deformation41. However, its high computational cost makes it impractical for the current study. We use LAMMPS simulation package for all computations71. All models in our numerical experiments are initially relaxed in the NPT ensemble using Nose-Hoover thermostat72 at 300 K and Parinello-Rahman barostat73 at 1 atm for 2 ns and time steps of 1 fs. After proper volumetric relaxation by inflicting 1000 cycles of volumetric stress perturbation of 0.1 GPa, we confirm a density of 2.59 g/cm3 in close agreements with SANS measurements54. Also we repeated the simulations for a system twice as large to observe the impact of size effects (Supplementary Fig. 3).
Incremental stress marching technique
Here, we envision a three-stage cyclic scheme that applies successive stress perturbations with varying average stress levels, which are kept within the elastic limits of the material. A complex system such as C-S-H has a rugged energy landscape40,43 as discussed in the results section and the core objective of this technique is to facilitate the evolution of the system to the low-lying minima from its current state using gradient-based energy optimization as demonstrated in Fig. 1a. Supplementary Note 2 and Supplementary Figs. 7–10 should be consulted for a simplified demonstration that the stress marching technique is equivalent to an inaccessibly long MD simulation.
Our approach continuously monitors the internal energy, enthalpy, stress, strain, and atomic trajectory in molecular models during loading (stage I), unloading (stage II), and reloading (stage III) phases, as demonstrated schematically in Fig. 1b. Strain is calculated as explained in Supplementary Note 3. In each individual stress cycle, the stress is perturbed about the mean value with increments of 0.01 GPa and an enthalpy minimization is carried out at the end of each increment. This is justified owing to the negligible effect of the entropic term in Gibbs free energy for a solid system such as C-S-H (G = H − TS where G, H and S are the Gibbs free energy, enthalpy and entropy of the system, also see Supplementary Note 4).
A threshold of ± 0.1 GPa is defined around the mean value and the loading direction is reversed when the limits of the envelope are reached. We use a total of 3 × 104 stress cycles in our ISM framework, which would ultimately lead to about 2 × 106 minimization steps. This staggering number of enthalpy minimizations signifies the infeasibility of eigenvalue-based minimizers that ensure convergence to a local minimum. However, unlike stress tapping approach74, our incremental updated Lagrangian method resolves an artifact of gradient-based minimizers, i.e., the possibility of converging to a saddle point. We note that the ISM technique is computationally expensive due to millions of enthalpy minimizations required in the process.
First, we note that the results presented in this paper, have been obtained based on a model prepared via a similar procedure as explained in Abdolhosseini Qomi et al.9. However, there are other more ordered models available in the literature such as those proposed by Kumar et al.66 and Kovačević et al.75. We have applied ISM to these models and also a completely crystalline sample of tombermorite and a similar behavior as the model used herein was observed (Supplementary Figs. 13–17 and Supplementary Note 5). This points to the fact that the layered structure and interlayer spacing can be taken as the main contributors to the time-dependent behavior of C-S-H and other minor structural modifications do not change the overall behavior.
The authors declare that the main data supporting the findings of this study are available within the article and its Supplementary Information files. Extra data are available from the corresponding author upon request.
Kassner, M. E. & Perez-Prado, M.-T. Fundamentals of creep in metals and alloys. (Elsevier, 2004).
Homer, E. R., Rodney, D. & Schuh, C. A. Kinetic Monte Carlo study of activated states and correlated shear-transformation-zone activity during the deformation of an amorphous metal. Phys. Rev. B 81, 64204 (2010).
Sha, Z. et al. Atomistic origin of size effects in fatigue behavior of metallic glasses. J. Mech. Phys. Solids 104, 84–95 (2017).
Bažant, Z. P. & Prasannan, S. Solidification theory for concrete creep. I: formulation. J. Eng. Mech. 115, 1691–1703 (1989).
Dönmez, A. & Bažant, Z. P. Shape factors for concrete shrinkage and drying creep in model B4 refined by nonlinear diffusion analysis. Mater. Struct. 49, 4779–4784 (2016).
Sinko, R., Vandamme, M., Bažant, Z. P. & Keten, S. Transient effects of drying creep in nanoporous solids: understanding the effects of nanoscale energy barriers. Proc. R. Soc. A 472, 20160490 (2016).
Vandamme, M. & Ulm, F. J. Nanoindentation investigation of creep properties of calcium silicate hydrates. Cem. Concr. Res. 52, 38–52 (2013).
Richardson, I. G. The calcium silicate hydrates. Cem. Concr. Res. 38, 137–158 (2008).
Pellenq, R. J.-M. et al. A realistic molecular model of cement hydrates. Proc. Natl. Acad. Sci. 106, 16102–16107 (2009).
Feldman, R. F. & Sereda, P. J. A new model for hydrated portland cement and its practical implications. Eng. J. 53, 53–59 (1970).
Jennings, H. M. Refinements to colloid model of C-S-H in cement: CM-II. Cem. Concr. Res. 38, 275–289 (2008).
Ioannidou, K. et al. Mesoscale texture of cement hydrates. Proc. Natl. Acad. Sci. 113, 2029–2034 (2016).
Ye, H. Creep mechanisms of calcium–silicate–hydrate: An overview of recent advances and challenges. Int. J. Concr. Struct. Mater. 9, 453–462 (2015).
Bažant, Z. P. & Osman, E. Double power law for basic creep of concrete. Mater. Constr. 9, 3–11 (1976).
Baweja, S. Creep and shrinkage prediction model for analysis and design of concrete structures— model B3. Mater. Struct. 28, 357–365 (1995).
Shahidi, M., Pichler, B. & Hellmich, C. Viscous interfaces as source for material creep: a continuum micromechanics approach. Eur. J. Mech. A/Solids 45, 41–58 (2014).
Li, X., Grasley, Z. C., Garboczi, E. J. & Bullard, J. W. Modeling the apparent and intrinsic viscoelastic relaxation of hydrating cement paste. Cem. Concr. Compos. 55, 322–330 (2015).
Baweja, S. Creep and shrinkage prediction model for analysis and design of concrete structures: Model B3, in ACI Concrete International. 83, 38–39 (2001).
Hubler, M. H., Wendner, R. & Bažant, Z. P. Comprehensive database for concrete creep and shrinkage: analysis and recommendations for testing and recording. Acids Mater. J. 112, 547–558 (2015).
Rahimi-Aghdam, S., Bažant, Z. P. & Abdolhosseini Qomi, M. J. Cement hydration from hours to centuries controlled by diffusion through barrier shells of C-S-H. J. Mech. Phys. Solids 99, 211–224 (2017).
Taylor, H. F. W. Nanostructure of CSH: current status. Adv. Cem. Based Mater. 1, 38–46 (1993).
Skinner, L. B., Chae, S. R., Benmore, C. J., Wenk, H. R. & Monteiro, P. J. M. Nanostructure of calcium silicate hydrates in cements. Phys. Rev. Lett. 104, 195502 (2010).
Cygan, R. T., Liang, J.-J. & Kalinichev, A. G. Molecular models of hydroxide, oxyhydroxide, and clay phases and the development of a general force field. J. Phys. Chem. B. 108, 1255–1266 (2004).
Shahsavari, R., Pellenq, R. J.-M. & Ulm, F.-J. Empirical force fields for complex hydrated calcio-silicate layered materials. Phys. Chem. Chem. Phys. 13, 1002–1011 (2011).
Galmarini, S., Kunhi Mohamed, A. & Bowen, P. Atomistic simulations of silicate species interaction with portlandite surfaces. J. Phys. Chem. C. 120, 22407–22413 (2016).
Durgun, E., Manzano, H., Pellenq, R. J. M. & Grossman, J. C. Understanding and controlling the reactivity of the calcium silicate phases from first principles. Chem. Mater. 24, 1262–1267 (2012).
Mishra, R. K. et al. cemff: A force field database for cementitious materials including validations, applications and opportunities. Cem. Concr. Res. 102, 68–89 (2017).
Masoumi, S., Valipour, H. & Abdolhosseini Qomi, M. J. Intermolecular forces between nanolayers of crystalline calcium-silicate-hydrates in aqueous medium. J. Phys. Chem. C. 121, 5565–5572 (2017).
Zhou, Y., Morshedifard, A., Lee, J. & Abdolhosseini Qomi, M. J. The contribution of propagons and diffusons in heat transport through calcium-silicate-hydrates. Appl. Phys. Lett. 110, 43104 (2017).
Abdolhosseini Qomi, M. J., Ulm, F.-J. & Pellenq, R. J.-M. Physical origins of thermal properties of cement paste. Phys. Rev. Appl. 3, 64010 (2015).
Qomi, M. J. A., Bauchy, M., Ulm, F. J. & Pellenq, R. J. M. Anomalous composition-dependent dynamics of nanoconfined water in the interlayer of disordered calcium-silicates. J. Chem. Phys. 140, 054515 (2014).
Shalchy, F. & Rahbar, N. Nanostructural characteristics and interfacial properties of polymer fibers in cement matrix. ACS Appl. Mater. Interfaces 7, (17278–17286 (2015).
Freddolino, P. L., Liu, F., Gruebele, M. & Schulten, K. Ten-microsecond molecular dynamics simulation of a fast-folding WW domain. Biophys. J. 94, L75–L77 (2008).
Peters, B. Reaction rate theory and rare events. (Elsevier Science, 2017).
Kushima, A., Eapen, J., Li, J., Yip, S. & Zhu, T. Time scale bridging in atomistic simulation of slow dynamics: Viscous relaxation and defect activation. Eur. Phys. J. B 82, 271–293 (2011).
Voter, A. F. Hyperdynamics: accelerated molecular dynamics of infrequent events. Phys. Rev. Lett. 78, 3908–3911 (1997).
Barducci, A., Bonomi, M. & Parrinello, M. Metadynamics. Wiley Interdiscip. Rev. Comput. Mol. Sci. 1, 826–843 (2011).
Lee, M. K. & Barr, B. I. G. An overview of the fatigue behaviour of plain and fibre reinforced concrete. Cem. Concr. Compos. 26, 299–305 (2004).
Richard, P., Nicodemi, M., Delannay, R., Ribière, P. & Bideau, D. Slow relaxation and compaction of granular systems. Nat. Mater. 4, 121–128 (2005).
Lacks, D. J. & Osborne, M. J. Energy landscape picture of overaging and rejuvenation in a sheared glass. Phys. Rev. Lett. 93, 1–4 (2004).
Manzano, H., Masoero, E., Lopez-Arbeloa, I. & Jennings, H. M. Shear deformations in calcium silicate hydrates. Soft Matter 9, 7333 (2013).
Malandro, D. L. & Lacks, D. J. Relationships of shear-induced changes in the potential energy landscape to the mechanical properties of ductile glasses. J. Chem. Phys. 110, 4593–4601 (1999).
Isner, B. A. & Lacks, D. J. Generic rugged landscapes under strain and the possibility of rejuvenation in glasses. Phys. Rev. Lett. 96, 1–4 (2006).
Königsberger, M., Irfan-ul-Hassan, M., Pichler, B. & Hellmich, C. Downscaling based identification of nonaging power-law creep of cement hydrates. J. Eng. Mech. 142, 4016106 (2016).
Phillips, J. C. Stretched exponential relaxation in molecular and electronic glasses. Rep. Prog. Phys. 59, 1133–1207 (1996).
Wu, J. H. & Jia, Q. The heterogeneous energy landscape expression of KWW relaxation. Sci. Rep. 6, 20506 (2016).
Palmer, R. G., Stein, D. L., Abrahams, E. & Anderson, P. W. Models of hierarchically constrained dynamics for glassy relaxation. Phys. Rev. Lett. 53, 958–961 (1984).
Yu, Y. et al. Stretched exponential relaxation of glasses at low temperature. Phys. Rev. Lett. 115, 1–5 (2015).
Liu, S. et al. Protein folding, binding and energy landscape: a synthesis. Protein. Eng. 207–252 (2012).
Zhu, T., Li, J. & Yip, S. Atomistic reaction pathway sampling: the nudged elastic band method and nanomechanics applications. in Nano and Cell Mechanics: Fundamentals and Frontiers 1st edn, 311–338 (John Wiley & Sons, Ltd, 2012).
Shih, J., Sheu, S. & Mou, C. A Voronoi polyhedra analysis of structures of liquid water. J. Chem. Phys. 100, 2202–2212 (1994).
Vandamme, M. & Ulm, F.-J. Nanogranular origin of concrete creep. Proc. Natl. Acad. Sci. 106, 10552–10557 (2009).
Ulm, F.-J. et al. Statistical indentation techniques for hydrated nanocomposites: concrete, bone, and shale. J. Am. Ceram. Soc. 90, 2677–2692 (2007).
Allen, A. J., Thomas, J. J. & Jennings, H. M. Composition and density of nanoscale calcium–silicate–hydrate in cement. Nat. Mater. 6, 311–316 (2007).
Soyer-Uzun, S., Chae, S. R., Benmore, C. J., Wenk, H.-R. & Monteiro, P. J. M. Compositional evolution of calcium silicate hydrate (C–S–H) structures by total X-ray scattering. J. Am. Ceram. Soc. 95, 793–798 (2012).
Dharmawardhana, C., Bakare, M., Misra, A., Ching, W. Y. & Bullard, J. Nature of interatomic bonding in controlling the mechanical properties of calcium silicate hydrates. J. Am. Ceram. Soc. 99, 2120–2130 (2016).
Masoumi, S., Valipour, H. & Abdolhosseini Qomi, M. J. Interparticle interactions in colloidal systems: toward a comprehensive mesoscale model. ACS Appl. Mater. Interfaces 9, (27338–27349 (2017).
Alizadeh, R., Beaudoin, J. J. & Raki, L. Viscoelastic nature of calcium silicate hydrate. Cem. Concr. Compos. 32, 369–376 (2010).
Miron, R. A. & Fichthorn, K. A. Multiple-time scale accelerated molecular dynamics: addressing the small-barrier problem. Phys. Rev. Lett. 93, 1–4 (2004).
Eyring, H. The activated complex in chemical reactions. J. Chem. Phys. 3, 107–115 (1935).
Jonsson, H., Mills, G. & Jacobsen, K. W. Nudged elastic band method for finding minimum energy paths of transitions. in Classical and Quantum Dynamics in Condensed Phase Simulations 385–404 (World Scientific,1998).
Fiocco, D., Foffi, G. & Sastry, S. Memory effects in schematic models of glasses subjected to oscillatory deformation. J. Phys. Condens. Matter 27, 194130 (2015).
Krakowiak, J. et al. Inference of the phase-to-mechanical property link via coupled X-ray spectrometry and indentation analysis: Application to cement-based materials. Cem. Concr. Res. 67, 271–285 (2015).
Abdolhosseini Qomi, M. J. et al. Combinatorial molecular optimization of cement hydrates. Nat. Commun. 5, 4960 (2014).
Geng, G., Myers, R. J., Qomi, M. J. A. & Monteiro, P. J. M. Densification of the interlayer spacing governs the nanomechanical properties of calcium-silicate-hydrate. Sci. Rep. 7, 10986 (2017).
Kumar, A. et al. The atomic-level structure of cementitious calcium silicate hydrate. J. Phys. Chem. C. 121, 17188–17196 (2017).
Kovačević, G., Persson, B., Nicoleau, L., Nonat, A. & Veryazov, V. Atomistic modeling of crystal structure of Ca1.67SiHx. Cem. Concr. Res. 67, 197–203 (2015).
Hamid, S. A. The crystal structure of the 11 A natural tobermorite. Z. Kristallogr. - New Cryst. Struct. 154, 189–198 (1981).
Beaudoin, J. J., Raki, L. & Alizadeh, R. A 29Si MAS NMR study of modified C-S-H nanostructures. Cem. Concr. Compos. 31, 585–590 (2009).
Chiang, W. S., Fratini, E., Baglioni, P., Liu, D. & Chen, S. H. Microstructure determination of calcium-silicate-hydrate globules by small-angle neutron scattering. J. Phys. Chem. C. 116, 5055–5061 (2012).
Plimpton, S. Fast parallel algorithms for short-range molecular dynamics. J. Comput. Phys. 117, 1–19 (1995).
Hoover, W. G. Canonical dynamics: equilibrium phase-space distributions. Phys. Rev. A. 31, 1695–1697 (1985).
Parrinello, M. & Rahman, A. Crystal structure and pair potentials: a molecular-dynamics study. Phys. Rev. Lett. 45, 1196–1199 (1980).
Bauchy, M. et al. Topological control on the structural relaxation of atomic networks under stress. Phys. Rev. Lett. 119, 1–5 (2017).
Kovačević, G., Nicoleau, L., Nonat, A. & Veryazov, V. Revised atomistic models of the crystal structure of C-S-H with high C/S ratio. Z. fur Phys. Chem. 230, 1411–1424 (2016).
M.J.A.Q. acknowledges startup funding from University of California, Irvine. The resources provided by the High Performance Computing (HPC) center at UCI are gratefully acknowledged. We are thankful to Dr. Matthieu Vandamme for his insightful comments on our work. We also note that the software VMD was developed by the Theoretical and Computational Biophysics Group in the Beckman Institute for Advanced Science and Technology at the University of Illinois at Urbana-Champaign.
The authors declare no competing interests.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Morshedifard, A., Masoumi, S. & Abdolhosseini Qomi, M.J. Nanoscale origins of creep in calcium silicate hydrates. Nat Commun 9, 1785 (2018). https://doi.org/10.1038/s41467-018-04174-z
This article is cited by
Communications Materials (2021)