This study investigates the hydration, microstructure, autogenous shrinkage, electrical resistivity, and mechanical properties of Portland cement pastes modified with PEG-PPG triblock copolymers with varied molecular weights. The early age properties including setting time and hydration heat were examined using the Vicat test and isothermal calorimetry. The hydration products and pore size distribution were analyzed using thermogravimetric analysis (TGA) and nitrogen adsorption, respectively. Mechanical properties and electrical resistivity were evaluated using the compressive strength test and electrochemical impedance spectroscopy (EIS). It was shown that the addition of the copolymers reduced the surface tension of the cement paste pore solution due to the presence of a hydrophobic block (PPG) in the molecular structure of the copolymers. The setting time and hydration heat were relatively similar in the control paste as well as the pastes modified with the copolymers. The results showed that copolymers were able to reduce the autogenous shrinkage in the paste due primarily to a reduction in pore solution surface tension. TGA showed a slight increase in the hydration degree of the paste modified with the copolymers. The compressive strength was reduced in the pastes modified with the copolymers that showed an increased volume of air voids. The addition of copolymers did not affect the electrical resistivity of the pastes except in the case where there was a large volume of air voids, which acted as electrical insulators.
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Evolution of the pore structure during the early stages of the alkali-activation reaction: an in situ small-angle neutron scattering investigation
The long-term durability of cement-based materials is influenced by the pore structure and associated permeability at the sub-micrometre length scale. With the emergence of new types of sustainable cements in recent decades, there is a pressing need to be able to predict the durability of these new materials, and therefore nondestructive experimental techniques capable of characterizing the evolution of the pore structure are increasingly crucial for investigating cement durability. Here, small-angle neutron scattering is used to analyze the evolution of the pore structure in alkali-activated materials over the initial 24 h of reaction in order to assess the characteristic pore sizes that emerge during these short time scales. By using a unified fitting approach for data modeling, information on the pore size and surface roughness is obtained for a variety of precursor chemistries and morphologies (metakaolin- and slag-based pastes). Furthermore, the impact of activator chemistry is elucidated via the analysis of pastes synthesized using hydroxide- and silicate-based activators. It is found that the main aspect influencing the size of pores that are accessible using small-angle neutron scattering analysis (approximately 10–500 Å in diameter) is the availability of free silica in the activating solution, which leads to a more refined pore structure with smaller average pore size. Moreover, as the reaction progresses the gel pores visible using this scattering technique are seen to increase in size.
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- Award ID(s):
- 1362039
- PAR ID:
- 10301629
- Date Published:
- Journal Name:
- Journal of Applied Crystallography
- Volume:
- 50
- Issue:
- 1
- ISSN:
- 1600-5767
- Page Range / eLocation ID:
- 61 to 75
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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