Tailorable thermal expansion in leucite-pollucite materials derived from geopolymers for environmental barrier coatings

The K[AlSi₂O₆]-Cs[AlSi₂O₆] pseudo-binary system was synthesized by geopolymer crystallization. The thermal expansion properties of these materials were studied by in situ high-temperature X-ray diffraction to characterize thermal expansion behavior for potential application as environmental barrier coatings. Tailorable thermal expansion through changing cation stoichiometry allowed reduced thermal expansion mismatch with SiC_f/SiC composites compared to rare-earth-based coatings.     

Ion Channels and Electroosmosis in Porous Geopolymers: A Novel Category of Low-Cost Memristors

Memristors are electric components that emulate the memory and computational properties of biological synapses by remembering the current that flows through them. Here, for the first time, the memristive properties of geopolymers, inexpensive ceramic materials manufactured at room temperature from alkaline activation of amorphous aluminosilicate precursors, are presented. It is demonstrated that geopolymers present all the fingerprints of memristors, and a physics-based model is proposed, which demonstrates that electroosmosis in the bulk geopolymer pores induces ion channels that foster change in the overall conductance of the bulk material, contributing to the observed memristive behavior. This model opens the door to a new category of porous electroosmosis-based bulk memristors. Synaptic functions such as short-term plasticity and long-term plasticity, as well as endurance and retention capabilities are also demonstrated. The reported findings pave the way to the use of geopolymers for low-cost applications in neuromorphic computing.     

Setting and nanostructural evolution of metakaolin geopolymer

The nanostructural evolution during formation of geopolymers and its correlation with setting have not been well understood. In this study, penetration resistance and ultrasonic wave reflection tests were conducted to measure setting, and solid‐state ²⁷Al NMR and liquid‐state ²⁹Si NMR were used to examine nanostructural changes in a metakaolin geopolymer as a function of time. Aluminum was released rapidly during the first 10 hour after mixing and immediately condensed with silicate species in solution to form larger sized aluminosilicate oligomers, which then condensed to form large structural units. Our evidence suggests these units form near metakaolin particle surface. Smaller sized silicate ions in the sol phase then attach to these units to form a gel with a more interconnected network structure. The initial stage of this attaching process was seen to be associated with set, which in this mixture occurred at 15 hour.     

Porous,Sintered Glass‐Ceramics from Inorganic Polymers Based on Fayalite Slag

The present paper deals with the synthesis of porous, sintered glass‐ceramics obtained at temperatures below 1150°C, originating from inorganic polymers based on fayalite slag. Firing led to the evaporation of water, dehydroxylation, and oxidation of Fe²⁺ above 345°C. For heating >700°C, the Si–O stretching band shifted from the 1160 and 750 cm^?1 to the 1255 and 830 cm^?1 region, due to a structural reorganization of the amorphous phase, whereas Fe–O bands appeared at 550 cm^?1. The final microstructure consisted predominantly of an amorphous phase, hematite, and franklinite. The open porosity and compressive strength decreased and increased, respectively, as the firing temperature increased. The final values suggest properties comparable to that of structural lightweight concrete, still, the materials synthesized herein, are lighter, and made primarily from secondary resources.     

Bio-derived sodium silicate for the manufacture of alkali-activated binders: Use of bamboo leaf ash as silicate source

Alkali activated binders are a promising alternative to the use of Portland cement in the manufacture of concrete for curbing CO₂ emissions. Novel sources of silicates have been investigated in recent years for reducing cost and environmental impacts associated with the use of chemical activators. This study describes the production of solid sodium silicate (SS) activating powder from bamboo leaf ash (BLA). Bamboo leaves were calcined at 550–800°C, mixed with NaOH pellets, and heated in an oven at 300°C. The obtained silicate powder was used for activating blended fly ash/slag samples. Mechanical and microstructural properties of BLA-based samples were compared to those of samples made with commercially available chemicals. The strength of BLA-activated mortars matched the commercially-sourced activators, being 25–30 MPa at 7 days and exceeding 40 MPa at 28 days. The microstructural analysis suggested that BLA-based SS showed a lesser degree of dissolution of precursors at 7 days, but the quality of the matrix was higher than that of NaOH-activated samples. These results confirmed that the reactivity of BLA-silicate powder was similar to that of commercial SS solutions, and show the potential valorization of future biomass renewable waste in the production of low carbon, alkali-activated concretes.     

原材料及工艺参数对土壤聚合物性能的影响

采用正交试验方法,全面研究了硅酸钠溶液模数、浓度,高岭土煅烧温度、煅烧时间以及液固比对土壤聚合物抗压强度、净浆扩展度和凝结时间的影响,并对土聚反应产物进行了初步探讨.研究结果表明:(1)各因素对土壤聚合物3 d抗压强度均有特别显著的影响;除了硅酸钠溶液模数外,其他因素都对土壤聚合物7 d抗压强度有特别显著的影响;只有液固比对土壤聚合物28 d抗压强度有特别显著的影响.(2)硅酸钠溶液浓度和液固比对土壤聚合物净浆扩展度的影响特别显著.(3)各因素对土壤聚合物凝结时间的影响不显著.(4)土聚反应生成的产物是无定形的,它可能是单硅铝酸土壤聚合物(PS)和双硅铝酸土壤聚合物(PSS)的复合物.     

From bulk to porous structures: Tailoring monoclinic SrAl2Si2O8 ceramic by geopolymer precursor technique

In this paper, monoclinic SrAl₂Si₂O₈ ceramics with porous structures were prepared based on ion-exchanged geopolymer precursor technique. Micron-level pores with a homogeneous pore-size distribution were introduced into the inorganic framework using foaming agents. The results demonstrated that the apparent density, pore-size distribution and specific surface area of porous geopolymer precursors can be well-engineered via tailoring the category and concentration of the foaming agent. After being treated at 900°C, hexagonal SrAl₂Si₂O₈ first-crystallized from the amorphous geopolymer matrix and then gradually converted into monoclinic SrAl₂Si₂O₈ between 1100°C and 1200°C. The resulting monoclinic SrAl₂Si₂O₈ ceramics maintained the porous structures during high-temperature treatments and exhibited high porosity, specific surface area, and compressive strength. The aforementioned strategy not only achieves monoclinic SrAl₂Si₂O₈ ceramics with well-defined and robust microstructures, but also provides an alternative route to prepare other porous ceramics, with potential applications in fields of high-temperature filters, adsorbents, and heterogeneous catalysis.     

Temperature stability of a pure metakaolin based K-geopolymer: Part 2. Variations in the mesoporous network and its rehydration stability

The thermal behavior of a model MK-based K-geopolymer was investigated between room temperature and 1400°C in order to evaluate its potentiality for high-temperature applications. The purpose of our study was to monitor the behavior of a geopolymer during a temperature rise in order to better understand its variations with respect to temperature. The works from the present paper focus only changes in the porous network; it follows a first part devoted to variations in the mineral matrix. The results obtained here show that the geopolymer material preserves its porous integrity up to 800°C, while maintaining the reversibility of water exchanges corresponding to about 25 weight percent. Together with the results of part 1, the findings of this study allow us to affirm that geopolymer materials are only very little affected by temperatures up to 800°C, or even 900°C (keeping its mesoporous amorphous structure).     

Rheology evolution of a geopolymer precursor aqueous suspension during aging

Geopolymer-based glass-ceramic matrix composites can be processed at room temperature and a heat treatment below 100°C leads to matrix hardening thanks to the geopolymerization mechanisms. The stabilization of the matrix into glass-ceramics is achieved via a post-curing at high temperature. This paves the way of the utilization of cost-effective liquid composite molding processes, for which all the necessary equipment is already available for processing temperature ranges related to polymer matrix composites, provided that the rheological behavior of the precursor is suitable to conveniently permeate the fibrous preform. The paper describes the thixotropic rheological behavior of a reference suspension at processing temperature (10°C-20°C) and its evolution along aging at −18°C. The changes are interpreted in terms of geopolymerization mechanisms (dissolution and polycondensation) and suspension rheology (predominance of hydrodynamic effects at high shear rate). On this basis, a phenomenological modeling framework, combining two Krieger-Dougherty equations, is proposed to build a relationship between the effective viscosity of the suspension and the phenomena involved during aging (dissolution of aluminosilicate particles) and shearing (microstructure scalar variable).