RESUMO
Cement and concrete are rapidly growing in demand and pose many unresolved chemistry questions at particle interfaces, during hydration reactions, regarding the role of electrolytes and organic additives. Solutions through developing greener, more sustainable formulations are needed to reduce the high carbon footprint that amounts to 11% of global CO2 emissions. Cement is a multiphase material composed of calcium silicates, aluminates, and other mineral phases, produced from natural and low-cost industrial sources, which undergoes complex hydration reactions. This perspective highlights current research challenges and opportunities for new chemistry insight, including intriguing colloid and interface science problems that involve mineral surfaces, electrolytes, polymers, and hydration reactions. Specifically, we discuss (1) characteristics of cement phases, supplementary cementitious materials, and other constituents, (2) hydration reactions and the characterization by imaging and NMR spectroscopy, (3) the structure of hydrated cement phases including calcium-silicate-hydrates at different scales, (4) quantitative simulation techniques from the atomic scale to microscale kinetic models, and (5) the function of organic additives. Focusing on new directions, we explain the benefits of integrating knowledge from inorganic chemistry, acid-base chemistry, polymer chemistry, reaction mechanisms, and theory to describe mesoscale cement properties and bulk properties upon manufacturing.
RESUMO
Three series of well-defined norbornene imide-based polymers with different pendant groups were synthesized to investigate the effect of the pendant group on the polymer conformation in solution and bulk melt properties. Each of these three series was examined by analyzing the polymers' bulk z-average radius of gyration via static light scattering and the polymers' melt viscoelastic properties via oscillatory measurements and differential scanning calorimetry. Sterically bulky pendant wedge groups modestly increase the rodlike conformation of the norbornene-imide polymer, however, the inherent rigidity of the polymer main-chain can still be observed with less bulky substituents. In stark contrast, the different side groups significantly impacted the bulk viscoelastic and thermal properties. By increasing the pendant group size, the chain diameter of the polymer increases and lowers the entanglement modulus. Finally, as the wedge pendant group size increases, the segmental relaxation time and the fragility index of these norbornene-based polymers are decreased.
