Abstract

To reduce the energy-intensity and carbon footprint of Portland cement (PC), the prevailing practice embraced by concrete technologists is to partially replace the PC in concrete with supplementary cementitious materials [SCMs: geological materials (e.g., limestone); industrial by-products (e.g., fly ash); and processed materials (e.g., calcined clay)]. Chemistry and content of the SCM profoundly affect PC hydration kinetics; which, in turn, dictates the evolutions of microstructure and properties of the [PC + SCM] binder. Owing to the substantial diversity in SCMs' compositions–plus the massive combinatorial spaces, and the highly nonlinear and mutually-interacting processes that arise from SCM-PC interactions–state-of-the-art computational models are unable to produce a priori predictions of hydration kinetics or properties of [PC + SCM] binders. In the past 2 decades, the combination of Big data and machine learning (ML)—commonly referred to as the fourth paradigm of science–has emerged as a promising approach to learn composition-property correlations in materials (e.g., concrete), and capitalize on such learnings to produce a priori predictions of properties of materials with new compositions. Notwithstanding these merits, widespread use of ML models is hindered because they: 1) Require Big data to learn composition-property correlations, and, in general, large databases for concrete are not publicly available; and 2) Function as black-boxes, thus providing little-to-no insights into the materials laws like theory-based analytical models do. This study presents a deep learning (DL) model capable of producing a priori, high-fidelity predictions of composition- and time-dependent hydration kinetics and phase assemblage development in [PC + SCM] pastes. The DL is coupled with: 1) A fast Fourier transformation algorithm that reduces the dimensionality of training datasets (e.g., kinetic datasets), thus allowing the model to learn intrinsic composition-property correlations from a small database; and 2) A thermodynamic model that constrains the model, thus ensuring that predictions do not violate fundamental materials laws. The training and outcomes of the DL are ultimately leveraged to develop a simple, easy-to-use, closed-form analytical model capable of predicting hydration kinetics and phase assemblage development in [PC + SCM] pastes, using their initial composition and mixture design as inputs.

Department(s)

Electrical and Computer Engineering

Second Department

Materials Science and Engineering

Comments

National Science Foundation, Grant 1661609

Keywords and Phrases

deep learning; hydration kinetic; prediction; sustaianability; thermodynamics

International Standard Serial Number (ISSN)

2296-8016

Document Type

Article - Journal

Document Version

Final Version

File Type

text

Language(s)

English

Rights

© 2023 The Authors, All rights reserved.

Creative Commons Licensing

Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.

Publication Date

04 Jan 2022

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