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Alkali-activated materials (AAMs) are candidates for high-strength lunar construction materials via in- situ resource utilization (ISRU) of aluminosilicate lunar regolith. To inform processing strategies for lunar AAMs, the shear-dependent rheological properties of a model AAM comprised of a sodium silicate activated metakaolin are measured from synthesis through gelation along with the compressive strength at longer reaction times. A combination of steady-shear, small amplitude oscillatory shear (SAOS), and Optimally Windowed Chirp (OWCh) techniques characterize the viscosity and shear moduli from initial slurry through the critical gel time. The critical gel point defines the processing time window regardless of the applied shear duration. Shearing prior to the critical gel point does not affect the critical gel time or viscoelastic properties of the material after the set point, or the 7-day compressive strength. However, the dynamic moduli prior to the critical gel time vary significantly based on the shear duration, and the critical gel exponent (n) increases with the duration of applied shear. These results demonstrate how to process without compromising final material properties. Metakaolin geopolymers exposed to low earth orbit (LEO) conditions on the Multi-purpose International Space Station Experiment Flight Facility (MISSE-FF) test station on the International Space Station (ISS) for six months of durability testing retain their compressive strength, furthering the technology readiness of aluminosilicate-derived construction material for future lunar construction. This study provides practical guidance for AAM processing protocols and insight into the effect of shear on the binder structural network valuable for both terrestrial and lunar ISRU 

Predicting the response of complex fluids to different flow conditions has been the focal point of rheology and is generally done via constitutive relations. There are, nonetheless, scenarios in which not much is known from the material mathematically, while data collection from samples is elusive, resource-intensive, or both. In such cases, meta-modeling of observables using a parametric surrogate model called multi-fidelity neural networks (MFNNs) may obviate the constitutive equation development step by leveraging only a handful of high-fidelity (Hi-Fi) data collected from experiments (or high-resolution simulations) and an abundance of low-fidelity (Lo-Fi) data generated synthetically to compensate for Hi-Fi data scarcity. To this end, MFNNs are employed to meta-model the material responses of a thermo-viscoelastic (TVE) fluid, consumer product Johnson’s® Baby Shampoo, under four flow protocols: steady shear, step growth, oscillatory, and small/large amplitude oscillatory shear (S/LAOS). In addition, the time–temperature superposition (TTS) of the material response and MFNN predictions are explored. By applying simple linear regression (without induction of any constitutive equation) on log-spaced Hi-Fi data, a series of Lo-Fi data were generated and found sufficient to obtain accurate material response recovery in terms of either interpolation or extrapolation for all flow protocols except for S/LAOS. This insufficiency is resolved by informing the MFNN platform with a linear constitutive model (Maxwell viscoelastic) resulting in simultaneous interpolation and extrapolation capabilities in S/LAOS material response recovery. The roles of data volume, flow type, and deformation range are discussed in detail, providing a practical pathway to multifidelity meta-modeling of different complex fluids. 

Electron transport in complex fluids, biology, and soft matter is a valuable characteristic in processes ranging from redox reactions to electrochemical energy storage. These processes often employ conductor–insulator composites in which electron transport properties are fundamentally linked to the microstructure and dynamics of the conductive phase. While microstructure and dynamics are well recognized as key determinants of the electrical properties, a unified description of their effect has yet to be determined, especially under flowing conditions. In this work, the conductivity and shear viscosity are measured for conductive colloidal suspensions to build a unified description by exploiting both recent quantification of the effect of flow-induced dynamics on electron transport and well-established relationships between electrical properties, microstructure, and flow. These model suspensions consist of conductive carbon black (CB) particles dispersed in fluids of varying viscosities and dielectric constants. In a stable, well-characterized shear rate regime where all suspensions undergo self-similar agglomerate breakup, competing relationships between conductivity and shear rate were observed. To account for the role of variable agglomerate size, equivalent microstructural states were identified using a dimensionless fluid Mason number, ${\mathit{Mn}}_f$, which allowed for isolation of the role of dynamics on the flow-induced electron transport rate. At equivalent microstructural states, shear-enhanced particle–particle collisions are found to dominate the electron transport rate. This work rationalizes seemingly contradictory experimental observations in literature concerning the shear-dependent electrical properties of CB suspensions and can be extended to other flowing composite systems.