Alkali Silicate Research Articles

Monitoring of historical structural materials with computed tomography

AbstractComputed tomography (CT) is an excellent tool to solve certain engineering problems connected to material science (such as sulfate swelling, internal degradation due to freezing, and alkali silicate swelling) and to understand specific processes (frost peeling, acid action). Albeit borne and mostly used in the medical domain, CT is increasingly used in the examination of the internal structure of building materials, where degradation processes occur to the detriment of their mechanical performance and durability. This paper presents five engineering problems concerning concrete freezing and thawing, concrete at high temperatures, timber charring, spalling in asbestos‐cement pipes, and deterioration in prestressed concrete pipes due to the corrosion of metallic inserts. In each case, the degradation processes are monitored via CT, something that may be crucial in the renovation and preservation of historical structures.

Effect of alkali dosage and silicate modulus on the deterioration of alkali-activated concrete properties subjected to sodium chloride attack and freeze thaw cycles

The deterioration mechanism of alkali-activated slag-fly ash-steel slag concrete (AAC) under sodium chloride attack and freeze-thaw (SF-T) cycles was investigated through a multi-scale methodology. Results showed that appropriate water glass modulus and higher Na2O dosage increased the compressive strength and salt-frost resistance of AAC. The mass loss in AAC was concentrated in the first 100 SF-T cycles, but PCC increases linearly with the SF-T cycles. The salt-frost resistance of PCC was similar to that of AAC samples Na2O dosage of 5 %. Higher Na2O dosage reduces the amount of unreacted precursor, thus reducing the porosity and improving the pore structure of concrete. However, increasing Na2O dosage has not limited the crack development, and the crack width in AAC was greater than in PCC after SF-T cycles. The porosity and average pore size of the concrete increased after SF-T cycles. Friedel's salt was only present in PCC, and NaCl crystals were observed in AAC.

Hybrid Organic-Inorganic Blast Furnace Slag Binders Activated with Alkali Acetates.

Hybrid organic-inorganic binders based on blast furnace slag were produced using sodium (NaAc) or potassium (KAc) acetate as the sole activator, and their properties were compared with those of sodium- or potassium hydroxide-activated slag pastes. The acetate-activated binders showed significantly lower cumulative heat release and extended setting time (∼230 h) than the hydroxide-activated binders. The main reaction products forming in all binders were calcium aluminosilicate hydrate-type gels and a hydrotalcite-like phase, independently of the activator type used. Compressive strengths of the acetate-activated pastes (∼40 MPa at 180 days) were lower than those of the hydroxide-activated binders (∼80 MPa at 180 days). However, the acetate-based binders exhibited superior impermeability and reduced wettability at 28 days, likely due to hydrophobic acetate groups. It is hypothesized that acetates dissociate in water, forming calcium acetate and alkali silicates via a reaction with species dissolving from the slag. This study demonstrates alkali acetates are effective activators for creating hybrid slag-based binders with reduced permeability.

Alkali Silicates Codoped with NIR-Emitting RE (Nd3+ and Yb3+) Ions for Thermometry Applications.

In the present study, the synthesis of BaSrSiO4 co-doped Yb3+ and Nd3+ nanophosphors (NPs) was successfully achieved through the conventional sol-gel method, as confirmed by X-ray diffraction and SEM analysis, verifying the formation of pure NPs. The FTIR and Raman spectra analysis confirm the formation of silicates, as different modes and vibrations of Si-O and Si-O-Si were seen at 800-1000cm-1. The energy transfer (ET) mechanism between Nd3+ and Yb3+ ions was seen as the emission spectra showed a rise in intensity of one over another. PLE emission spectra showed transitions at 2F7/2-2F5/2 for Yb3+ and from 4F3/2 to (4I9/2, 4I11/2, and 4I13/2) for Nd3+ when excited at 785nm. All the samples record low activation energy, which shows that the rate of reaction will be higher in all the samples, and it will be highest for 1mol% Nd3+ and 1mol% Yb3+. An increasing value of τ was seen with increasing Yb3+ concentration, which confirms the increase in the population of trap centers. The positron annihilation lifetime (PAL) curve showed that 1mol% Yb3+ and 2mol Nd3+ have single vacancies or shallower positron traps, whereas 3mol% Yb3+ and 2mol% Nd3+ have larger defects like surface oxygen vacancy clusters. The other two samples have balance vacancies, which makes them best for thermometry applications. The fluorescence intensity ratio (FIR) was calculated to get sensitivity for thermometry application. 2.13% K-1 sensitivity achieved at 303-333K temperature.

The Utilisation of Rice Husk Ash Leachates for The Synthesis of Eco-Friendly Geopolymers

Geopolymers are inorganic polymers projected as feasible alternatives to Portland cement due to their lower CO2 emissions and high mechanical properties. In recent times, however, their impact on other environmental indices such as abiotic depletion, freshwater toxicity, marine ecotoxicity, terrestrial ecotoxicity, acidification, and human toxicity has become questionable, thus the need to investigate alternative eco-friendly precursors and activators. This work aims to manufacture an eco-efficient geopolymer by utilising biomass ash leachate as an alternative to the conventional alkali silicate solution. The leachate was obtained by soaking the rice husk ash (RHA) in a 10 M concentration of NaOH solution and filtering to obtain a clear solution. The effects of the calcination temperature of the kaolin and the RHA content in the alkaline solution were investigated, and a factorial design of experiments was developed considering three levels of calcination temperature (700°C, 800°C, and 900°C) and five levels of RHA content (0 g, 5 g, 10 g, 15 g, and 20 g). Physical and mechanical tests were performed on the synthesised geopolymer pastes, and chemical analysis was performed using X-ray diffraction and X-ray spectroscopy. The impacts of replacing the synthetic alkali silicates with rice husk ash-based activators were compared. The results showed that the calcination temperature of the kaolin and the content of the RHA both contributed significantly to the flexural and compressive strength at the 0.01 level of significance. A compressive strength of 10.4 MPa was obtained for the MK915 binders, which showed a 100% increase from samples without RHA content. This research proves that utilising RHA-based activators in metakaolin-based geopolymers can be feasible for less critical applications where a very high compressive strength will not be required.Keywords: alkaline activators, biomass, geopolymers, leachates, rice husk ash

The distribution and generation of carbonatites

The physio-chemical framework that generates carbonatites and, ultimately, the associated rare earth element deposits remains contentious. This primarily reflects the diverse tectonic settings in which carbonatites occur: large igneous provinces, continental rifts and major extensional terranes, syn- to post-collisional settings, or ocean islands. There is, however, a broad consensus that carbonatites (or their parental melts) originate in the mantle. These exotic melts have small volumes that make them ideal probes of conditions in their underlying source regions. We combine the carbonatite locations with global maps of lithospheric thickness, derived from seismic tomography, and show that post-Neoproterozoic carbonatites occur preferentially above the margins of thick cratonic lithosphere (e.g., adjacent to the South Atlantic and Indian Oceans or in North America, Greenland, and Asia) and where once thick lithosphere has undergone stretching (e.g., eastern Asia). Our thermal modeling reveals that lateral and vertical heat conduction on rifted craton margins, or rapid stretching of cratonic lithosphere, can mobilize carbonated peridotite at the temperatures (950−1250 °C) and pressures (2−3 GPa) required to form primary carbonatites or their parental alkali silicate melts. Importantly, our models show that heat conduction from upwelling mantle plumes or ambient mantle on rifted cratonic margins may sufficiently modify the temperature of the lithospheric mantle to cause melting of carbonated peridotite, settling the long-standing debate on the role of rifting and heating in the generation of carbonatites.

Nundorite: a geological oddity of critical minerals significance from the Mount Arrowsmith Volcanics, northwestern NSW

Nundorite is a unique and enigmatic rock type, known only from its type locality within the Koonenberry Belt of western NSW. The rock is highly anomalous in geochemical composition being peralkaline, with low silica and high alumina, but enriched in rare metals such as Zr, Nb and rare earth elements. This study presents a comprehensive mineralogical and geochemical study of nundorite to resolve its origins and its potential to inform on the geological processes that lead to critical metal concentration in the crust. Nundorite is found only at a single outcrop but shows a progression of alteration and deformation over ∼250 m from the northwest to southeast. The least deformed varieties consist of coarse aegirine grains within a matrix composed predominantly of natrolite and microcline with minor albite, nepheline and schizolite. With increasing deformation, the proportion of albite and aegirine decreases, the primary zeolite changes from natrolite to analcime, and the pyroxene and schizolite shift towards the aegirine and serandite (Mn-rich) endmember compositions, respectively. These transitions can be related to progressive hydration and recrystallisation of the rock in response to hydrothermal alteration associated with deformation. Nundorite also contains a diverse suite of accessory rare metal phases such as zircon, monazite, cerite-group minerals, fergusonite, fersmite, natroniobite, galgenbergite, epidote–allanite and a range of Zr alkali silicate minerals. Samarium–Nd isotopic compositions of nundorite (εNd ∼+5.5 at 585 Ma) are comparable with mafic volcanic rocks of the surrounding Mount Arrowsmith Volcanics and are consistent with derivation from a mantle source. These data, together with the uniform peralkaline composition, depletion in Ti and P, and enrichment in incompatible elements, are consistent with an origin as highly fractionated phonolite. Phonolites of similar composition are rare but have been reported from continental rift and intraplate alkaline provinces worldwide. Nundorite, therefore is not just a geological oddity, but also provides reaffirmation of the continental rift setting for the Mount Arrowsmith Volcanics and highlights the critical mineral resource potential of the region, as extensive crystal fractionation is a key mechanism to produce ore grade levels of rare metals in alkaline magmatic systems.

Preparation of Geopolymeric Materials from Industrial Kaolins, with Variable Kaolinite Content and Alkali Silicates Precursors.

In the present work, the development of geopolymeric materials with Na or K based on industrial kaolin samples, with variable kaolinite content and alkaline silicates, is studied. XRF, XRD, FTIR and SEM-EDS have been used as characterization techniques. Three ceramic kaolin samples, two from Algeria and one from Charente (France), have been considered. In particular, chemical and mineralogical characterization revealed elements distinct of Si and Al, and the content of pure kaolinite and secondary minerals. Metakaolinite was obtained by grinding and sieving raw kaolin at 80 μm and then by thermal activation at 750 °C for 1 h. This metakaolinite has been used as a base raw material to obtain geopolymers, using for this purpose different formulations of alkaline silicates with NaOH or KOH and variable Si/K molar ratios. The formation of geopolymeric materials by hydroxylation and polycondensation characterized with different Si/Al molar ratios, depending on the original metakaolinite content, has been demonstrated. Sodium carbonates have been detected by XRD and FTIR, and confirmed by SEM-EDS, in two of these geopolymer materials being products of NaOH carbonation.

Alkali-silica reaction of ferronickel slag fine aggregate in Portland cement and alkali-activated slag mortars: Pessimum effect investigation

Ferronickel slag (FNS) with dense and hard nature exhibits great potential to be utilized as recycled aggregate in concrete production. This study investigated the alkali-silica reaction (ASR) and the pessimum proportion of FNS fine aggregate in Portland cement (PC) and alkali-activated ground granulated bast furnace slag (AAS) mortars as a substitute for river sand. Over a 120-day period, the accelerated mortar bar test revealed that the addition of FNS fine aggregate in both cases resulted in harmless ASR expansion. In PC mortars, the ASR expansion consistently decreased from 0.569 % to 0.114 % as the FNS content increased. In comparison, AAS mortars with higher pore solution alkalinity had the pessimum proportion of 30 % FNS. The ASR expansion values initially increased from 0.472 % to 0.554 % with an increase in FNS content from 0 % to 30 %, but then decreased to 0.146 % as the FNS content was further raised to 100 %. The amorphous ASR gel was identified as a hydrated alkali silicate gel and present within the existing veins in the river sand grain. The ASR reaction of FNS fine aggregate exhibited a self-mitigating effect on the deleterious expansion through its pessimum behavior. Additionally, the addition of FNS fine aggregate yielded a beneficial outcome by reducing the cumulative pore volume in the mortars, and thus enhanced the compressive strengths.

Improvements in Hydrolytic Stability of Alkali-Activated Mine Tailings via Addition of Sodium Silicate Activator.

Over 14 billion tons of mine tailings are produced throughout the world each year, and this type of waste is generally stored onsite indefinitely. Alkali activation is a promising strategy for the reuse of mine tailings to produce construction materials, converting this waste stream into a value-added product. One major problem with alkali-activated mine tailings is their low durability in water (i.e., low hydrolytic stability). In this article, the influence of a mixed sodium hydroxide/sodium silicate alkali activator on the compressive strength, hydrolytic stability, and microstructure of alkali-activated materials (AAMs) were systematically investigated. XRD, FTIR, NMR, and NAD were used to investigate microstructural changes, and a water immersion test was used to show improvements in hydrolytic stability. For gold mine tailings activated with pure sodium hydroxide, the compressive strength was 15 MPa and a seven-day water immersion test caused a strength loss of 70%. With an addition of 1 M sodium silicate in the activator, the AAMs achieved a compressive strength of over 30 MPa and strength loss of only 45%. This paper proposes a mechanism explaining why the strength and hydrolytic stability of AAMs are dependent on the dosage of soluble silicate. A high dosage of sodium silicate inhibits the depolymerization of the source material, which results in a sample with less amorphous aluminosilicate gel and, therefore, lower hydrolytic stability.

Synergistic protection of borate and silicate salts composite for controlling the chloride-induced pitting and uniform corrosion of steel reinforcement bars embedded in mortars

In this study, the efficacy of the combined effect of borate and silicate alkali metal salts added to mortars for controlling the chloride-induced uniform and localized corrosion of embedded steel rebars is examined. The individually added salts in mortars are found to have insignificant effects in terms of reducing the uniform corrosion rate and localized damage. However, their combination (0.50% sodium tetra borate + 0.10% sodium silicate added with respect to the weight of the binder) provides complete protection to reinforcements tested for long durations under wet/dry treatments with mortars in saline water and laboratory atmospheres. Electrochemical impedance spectroscopy, direct current cyclic polarization, polarization resistance, and visual observations are used for quantitative and qualitative evaluations of the protective effects of the tested additives. X-ray diffraction analysis, scanning electron microscopy, and energy-dispersive X-ray spectroscopy analysis of the corrosion products formed on the embedded steel surfaces help explain the possible mechanisms behind the considerable improvement in the inhibitive effects of a mixed composition of borate and silicate. This combination also improves the compressive strength and workability of the mixed concrete. The results reveal that the synergistic protection provided by a mixture of borate and silicate can be attributed to the co-deposition of an iron-boron + ferrosilicate + cortensitite (an iron-silicon phase) film on the rebar surface.

Research of the New Laboratory Methodology for Measuring the Disintegration of Mixtures with Inorganic Binders Hardened by Dehydration

The paper deals with the possibilities of using alkali silicate based inorganic binders for automotive industry aluminium castings production. In recent years, inorganic binders are coming back to the foreground and their manufacturers are developing new processes, which are starting to progressively supersede organic binder systems. Paper describes known knowledge about classic alkali silicate binders with focus on hardening processes and on improving their technological properties. Trends from the area of development and the use new alkali silicate based inorganic binders are also shortly described. As part of the experimental work, specific methods of producing samples were developed, with the help of which properties such as disintegration were subsequently evaluated by measuring abrasion and residual strengths. Characteristics such as residual compressive strength or shear strength at different thermal loads were also evaluated. When comparing the laboratory results with the results of de-coring in real conditions, a high degree of correlation was achieved, which makes it possible to determine the optimal recipe/procedure for the production of geometrically complex cores.

Geopolymers made using organic bases. Part I: Synthesis and atomic structure

AbstractGeopolymers can act as a facile forming route to aluminosilicate ceramic composites due to being processed as fluids rather than as powders. However, the compositions available via typical alkali geopolymers are limited by the presence of alkali cations, introduced by the alkali silicate solution precursors. In order to expand the ceramic compositions that are accessible by geopolymer processing, this study explored the use of three strong organic bases (guanidine, tetramethylguanidine [TMG], and tetramethylammonium hydroxide [TMAOH]) as alternatives to inorganic alkali hydroxides in geopolymer synthesis. Silicate solutions were able to be produced with all three bases and favorable silica speciation was identified in the guanidine and TMG silicate solutions. Monolithic bodies were produced using guanidine and TMAOH, while no TMG samples hardened. By 27Al and 29Si nuclear magnetic resonance spectroscopy and powder X‐ray diffraction, the guanidine samples were determined to be structurally similar to those made using sodium hydroxide and hence can be called geopolymers, while the solids made with TMAOH were not structurally similar to sodium geopolymers and contained one or more unknown phases. This study has demonstrated that geopolymers can be made using organic bases rather than alkali hydroxides and that the speciation of dissolved silica alone does not indicate that an organic base silicate solution will be reactive.

Effects of the alkali metal oxides and bed material compositions on agglomeration phenomena in CFB boiler

Circulating fluidized bed boiler is environmentally friendly technology in power generation. However, agglomeration related operational standard has not been established yet. As a basis of establishing standard, the fixed bed agglomeration mechanism of bed inventory was investigated. The melting temperature reduction occurred with induced change of alkali metal compositions. The melting temperature reduction result in viscous surface on particles and ease of being agglomerated. The temperature reduction appeared more clearly in silica sand than bottom ash. This was caused by the high SiO2 composition of the sand and alkali silica reaction occurred because activated alkali compositions were reacted with SiO2 forming alkali silicates. Further analyses of agglomerates produced in bubbling fluidized bed reactor were conducted. The expected agglomeration effect has similar trend with melting temperature reduction. And the agglomeration effect appeared more in silica sand because of high SiO2 composition and sodium was more effective in forming agglomerates than potassium. Therefore, bottom ash can replace silica sand as bed material in CFB boiler. And sodium composition must be managed more strictly than potassium composition.

Inorganic intumescing alkali silicate particles

New generation intumescent coatings apply self-intumescing particles to induce expansion in a controlled manner. Various studies have investigated alkali silicate-based coatings due to their inherent expansion with the release of H2O. The presented work investigated the self-intumescing concept of alkali silicates as particles. A thorough study of inorganic alkali silicate particles as potential intumescent ingredients in passive fire protection systems was carried out by applying HSDM, TGA, FTIR, XRD, and SEM. Herein, particles of lithium-, sodium-, and potassium silicates were synthesized with varying silica-to-alkali oxide molar ratios and curing humidity. Subsequently, the hydration chemistry and thermal behavior were examined. The results revealed increased expansion potential with decreasing SiO2/M2O molar ratio (M = Na, Li, or K) in the range 3.1–7.4 and increasing curing humidity in the range 35, 50, and 90% RH. Previous studies have emphasized the effect of solid-bound H2O to induce intumescence. In this study, the influence of the softening of the silicate matrix and H2O release is highlighted to allow increased expansion potential. Here, the coupling of thermal analysis with microscopy suggests an intumescence mechanism in the order of 1) initial shrinkage due to loss of free and physical bound H2O, 2) sphere formation to minimize surface energy, 3) expansion as a result of H2O evolution and viscoelastic melt formation, and 4) second shrinkage due to sintering before 5) melting. The sodium alkali silicate particles with a SiO2/M2O molar ratio of 3.4 exhibited a timely softening of the silicate matrix from about 155 °C to provide a distinct spherical particle followed by ionic H2O evolution. As a result, hereof, hollow, spherical particles with relative solid expansions of up to 550% were obtained and maintained until a second shrinkage at 650 °C with a subsequent melting at 950 °C. In comparison, the imbalance in viscoelastic melt formation and H2O release of lithium- and potassium silicate particles resulted in less expansion. Considering the expansion potential and thermal behavior of the alkali silicate particles, it is suggested as a possible, sustainable intumescence ingredient.

An Experimental Study on Performance of Two-Part Geopolymer Concrete Using Natural Binders and Activators

The study investigates the characteristics of geopolymer concrete, employing sodium silicate and sodium hydroxide as activators instead of cement. In conventional construction practices, binders like fly ash, ground granulated blast furnace slag (GGBS) are commonly combined with alkali solutions. The manufacturing process of geopolymer relies on various alkaline activators. In this research, GGBS is replaced with sodium hydroxide and sodium silicate as activators. GGBS is recognized for its ability to enhance the workability and strength of geopolymer concrete, exhibiting favorable mechanical properties, resistance to chemicals, minimal shrinkage, environmental friendliness and exceptional durability. Furthermore, there are still certain drawbacks to geopolymer concrete, such as the fact that alkaline solutions are difficult to handle and apply because they are viscous, corrosive, difficult to transport, as well as challenging to store in huge quantities. A two part geopolymer concrete consists of two main components. An activator solution and a binder solution. The activator solution typically contains alkali metal hydroxides or silicates, while the binder solution contains aluminosilicate material such as fly ash or metakaolin. When mixed together, these solutions undergo a chemical reaction that forms a solid and durable geopolymer material.

Designed functions of oxide/hydroxide nanosheets via elemental replacement/doping.

Partial replacement of one structural element in a solid with another of a similar size was conducted to impart functionality to the solids and modify their properties. This phenomenon is found in nature in coloured gemstones and clay minerals and is used in materials chemistry and physics, endowing materials with useful properties that can be controlled by incorporated heteroelements and their amounts. Depending on the area of research (or expected functions), the replacement is referred to as "isomorphous substitution", "doping", etc. Herein, elemental replacement in two-dimensional (2D) oxides and hydroxides (nanosheets or layered materials) is summarised with emphasis on the uniqueness of their preparation, characterisation and application compared with those of the corresponding bulk materials. Among the 2D materials (graphene, metallenes, transition metal chalcogenides, metal phosphate/phosphonates, MXenes, etc.), 2D oxides and hydroxides are characterised by their presence in nature, facile synthesis and storage under ambient conditions, and possible structural variation from atomic-level nanosheets to thicker nanosheets composed of multilayered structures. The heteroelements to be doped were selected depending on the target application objectively; however, there are structural and synthetic limitations in the doping of heteroelements. In the case of layered double hydroxides (single layer) and layered alkali silicates (from single layer to multiple layers), including layered clay minerals (2 : 1 layer), the replacement (commonly called isomorphous substitution) is discussed to understand/design characteristics such as catalytic, adsorptive (including ion exchange), and swelling properties. Due to the variation in their main components, the design of layered transition metal oxide/hydroxide materials via isomorphous substitution is more versatile; in this case, tuning their band structure, doping both holes and electrons, and creating impurity levels are examined by the elemental replacement of the main components. As typical examples, material design for the photocatalytic function of an ion-exchangeable layered titanate (lepidocrocite-type titanate) and a perovskite niobate (KCa2Nb3O10) is discussed, where elemental replacement is effective in designing their multiple functions.

Temperature Dependence and Prediction of Density of Alkali Silicate Slag Melts

Temperature Dependence and Prediction of Density of Alkali Silicate Slag Melts

Structure and chemical durability improvement of alkali silicate glass by zirconium dioxide and erbium oxide addition

Glass structure tailoring of alkali silicate glasses by addition of ZrO2 and Er2O3 is found to enhance the chemical durability of glasses. ZrO2 (x ranged between 5 mol% to 15 mol%) and Er2O3 (y ranged between 0.5 mol% to 1.5 mol%) were used to replace SiO2 and Na2O, respectively, in the glasses with the nominal composition of 10Li2O-(15-y)Na2O-10CaO-(65-x)SiO2-xZrO2-y Er2O3. The samples were prepared by conventional melt quenching technique. The structures of produced glasses were examined by X-ray absorption spectroscopy (XAS) and Raman spectroscopy. XAS spectra demonstrated that the oxidation numbers of Zr and Er ions were +4 and +3, respectively. The chemical environment around both cations was six-fold coordination. In addition, Raman spectra demonstrated that the Zr4+ ions formed the Q4(Zr) structure, which caused the reduction of non-bridging oxygen. In case of the Er3+ ions, the formation of the Si-O-Er bonds was explained from the Raman study. The chemical durability of glass was determined from Na+ ions leaching values. In pH 7 solution, the leached Na+ ions reduced from 25.67% to 21.43% and from 22.50% to 20.49% as a function of concentration of ZrO2 (x = 5 mol% to 15 mol%) and Er2O3 (y = 0.5 mol% to 1.5 mol%), respectively. As the results, the chemical durability of the ZrO2-containing and Er2O3-containing glasses were significantly improved due to charge compensated mechanism and enhancing network rigidity by increasing cation field strength. Moreover, the micro-hardness (580 HV to 837 HV) and density (2.54 g⸳cm-3 to 2.82 g⸳cm-3) also displayed an increased tendency with larger concentration of ZrO2 and Er2O3.

Evidence for Complex Dynamics in Glassy Fast Ion Conductors: The Case of Sodium Thiosilicates.

Classical molecular dynamics is used to study the dynamics of alkali ions in a promising fast ion conductor glass system, i.e., Na2S-SiS2. Diffusion in such thiosilicates is found to display various salient features of alkali silicates, i.e., channel-like diffusion with typical length scales emerging as the temperature is decreased to the glassy state, and Arrhenius behavior for both Na ion diffusivity and calculated conductivity. The dynamics appears, however, to be largely heterogeneous as manifested by fast and slow Na ion motion at intermediate times, both in the high-temperature liquid and in the glassy state. In the former, a diffusion-limited regime is found due to the increased motion of the network-forming species that limits the Na ion dynamics, whereas at low temperatures, the typical dynamical heterogeneities are recovered as observed close to the glass transition.