Modification of poly(ethylene glycol) on the microstructure and mechanical properties of calcium silicate hydrates. (January 2019)

• Record Type: Journal Article
• Authors: Zhou, Yang; Orozco, Carlos A.; Duque-Redondo, Eduardo; Manzano, Hegoi; Geng, Guoqing; Feng, Pan; Monteiro, Paulo J.M.; Miao, Changwen
• Is Part Of: Cement and concrete research. Volume 115(2019)
• Page Start: 20
• Page End: 30
• Publication Date: 2019-01
• Subjects: Calcium-silicate-hydrate -- Microstructure -- Mechanical properties -- High-pressure X-ray diffraction -- Composite; Cement -- Periodicals; Cement -- Research -- Periodicals; Concrete -- Periodicals; Concrete -- Research -- Periodicals; Ciment -- Périodiques; Béton -- Périodiques; Cement; Concrete; Periodicals; 620.135
• DOI: 10.1016/j.cemconres.2018.10.001
• Languages: English
• ISSNs: 0008-8846

Abstract

Abstract: With the aim of creating more sustainable building materials, calcium silicate hydrate (C-S-H), the primary binding phase in modern concrete, was integrated with poly(ethylene glycol) (PEG). At the crystal lattice scale, synchrotron radiation-based high-pressure X-ray diffraction (HP-XRD) reveals that the incorporation of PEG increases the ab-planar stiffness of C-S-H leading to a higher bulk modulus, while molecular simulation results indicate polymers are not likely intercalated into the interlayer region. At a higher length scale, nanoindentation measurements show the introduction of PEG lowers the packing density of C-S-H particles and, thus, decreases the indentation modulus. However, a high creep resistance of the C-S-H/PEG sample is still maintained, which suggests a meso-composite may form to restrict the rapid translation between neighboring calcium silicate sheets. Furthermore, 29 Si nuclear magnetic resonance (NMR) shows that the presence of PEG shortens the mean chain length of C-S-H, making dimer the predominant structure.