Search Results (14)

In order to cope with the emergence of energy conservation and consumption reduction initiatives, we used an acrylic emulsion (as the adhesive), combined with silica aerogel (SA) and hollow glass microsphere (HGM) fillers, to synthesize thermal insulation coatings, which were found to have low thermal conductivity and excellent thermal insulation properties. These waterborne coatings are environmentally friendly and were synthesized without organic solvents. Comprehensive testing verified that the coatings met practical requirements. Specifically, the addition of 18% SA resulted in minimal thermal conductivity (0.0433 W/m·K), the lowest density (0.177 g/cm³), as well as a reduced gross calorific value. At a heating surface temperature of 200 °C, the 5 mm coating’s cooling surface temperature was 108.7 °C, yielding a 91.3 °C temperature difference and demonstrating remarkable thermal insulation performance. Furthermore, the coatings showed favorable results in terms of water resistance, corrosion resistance, wear resistance, and adhesion, achieving satisfactory engineering standards. In this work, the influence of different contents of SA on various properties of the coating was studied, with the aim of providing a reference for the modulation of the comprehensive performance of SA thermal insulation coatings. Full article

To expand the applications of hydrophobic silica aerogels derived from rice husk ash (HSA) through simple traditional methods (without adding special materials or processes), this paper employs machine learning to establish mathematical models to identify optimal conditions for extracting water glass and investigates how preparation conditions and heat treatment temperatures affect properties such as the porosity and hydrophobicity of HSA. The results indicate that the decision tree regression model provides the most accurate predictions for the extraction rate and modulus of water glass. Notably, the water contact angle of HSA produced using nitric acid as a catalyst can reach as high as 159.5°, classifying it as a superhydrophobic material. Additionally, while moderately increasing the concentration of the hydrophobic modifier enhances HSA’s hydrophobicity, it concurrently reduces its porosity. The HSA maintained hydrophobicity until 500 °C. The pore structure of HSA collapsed gradually with the increase in heat temperature. After treatment at 700 °C, HSA lost its hydrophobicity and the porous structure was severely damaged. Compared with silica aerogel using traditional silicon sources, the damage to pore structure and the crystallization occurred at lower temperatures, but the hydrophobicity remained at higher temperatures. Full article

Due to their high surface area and low weight, silica aerogels are ideally suited for several uses, including drug delivery, catalysis, and insulation. Oil–water–oil (OWO) double emulsion is a simple and regulated technique for encasing a volatile oil phase in a silica shell to produce hollow silica (SiO₂) aerogel particles by using hydrophilic and hydrophobic emulsifiers. In this study, the oil–water–oil (OWO) double emulsion method was implemented to synthesize surface-modified hollow silica (SiO₂) aerogel particles in a facile and effective way. This investigation mainly focused on the influence of the N-hexane-to-water glass (OW) ratio (r) in the first emulsion, silica (water glass) content concentration (x), and surfactant concentration (s) variations. Furthermore, surface modification techniques were utilized to customize the aerogel’s characteristics. The X-ray diffraction (XRD) patterns showed no imprints of impurities except SiO₂. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images highlight the hollow microstructure of silica particles. Zeta potential was used to determine particle size analysis of hollow silica aerogel particles. The oil–water–oil (OWO) double emulsion approach was successfully employed to synthesize surface-modified hollow silica (SiO₂) aerogel particles, providing precise control over the particle characteristics. By the influence of the optimization condition, this approach improves the aerogel’s potential applications in drug delivery, catalysis, and insulation by enabling surface modifications. Full article

In the automotive industry, there has been considerable focus on developing various sensors for engine oil monitoring. However, when it comes to monitoring the condition of brake fluid, which is crucial for ensuring safety, there has been a lack of a secure online method for this monitoring. This study addresses this gap by developing a hybrid silica nanofiber mat, or an aerogel integrated with an optical fiber sensor, to monitor brake fluid condition. The incorporation of silica nanofibers in this hybrid enhances the sensitivity of the optical fiber glass surface by at least 3.75 times. Furthermore, creating an air gap between the glass surface of the optical fiber and the nanofibers boosts sensitivity by at least 5 times, achieving a better correlation coefficient (R² = 0.98). In the case of silica aerogel, the sensitivity is enhanced by 10 times, but this enhancement relies on the presence of the established air gap. The air gap was adjusted to range from 0.5 mm to 1 mm, without any significant change in the measurement within this range. The response time of the developed sensor is a minimum of 15 min. The sensing material is irreversible and has a diameter of 2.5 mm, making it easily replaceable. Overall, the sensor demonstrates strong repeatability, with approximately 90% consistency, and maintains uncertainty levels below 5% across specific ranges: from 3% to 6% for silica aerogel and from 5% to 6% for silica nanofibers in the presence of an air gap. These findings hold promise for integrating such an optical fiber sensor into a car’s electronic system, enabling the direct online monitoring of brake fluid quality. Additionally, the study elucidates the effect of water absorption on the refractive index of brake fluid, as well as on the silica nanomaterials. Full article

The aim of this study is to reduce the manufacturing cost of a hydrophobic and heat-insulating silica aerogel and promote its industrial application in the field of thermal insulation. Silica aerogels with hydrophobicity and thermal-insulation capabilities were synthesized by using water-glass as the silicon source and supercritical drying. The effectiveness of acid and alkali catalysis is compared in the formation of the sol. The introduction of sodium methyl silicate for the copolymerization enhances the hydrophobicity of the aerogel. The resultant silica aerogel has high hydrophobicity and a mesoporous structure with a pore volume exceeding 4.0 cm³·g⁻¹ and a specific surface area exceeding 950 m²·g⁻¹. The obtained silica aerogel/fiber-glass-mat composite has high thermal insulation, with a thermal conductivity of less than 0.020 W·m⁻¹·K⁻¹. The cost-effective process is promising for applications in the industrial preparation of silica aerogel thermal-insulating material. Full article

With the rapid development of industry and the acceleration of urbanization, oil pollution has caused serious damage to water, and its treatment has always been a research hotspot. Compared with traditional adsorption materials, aerogel has the advantages of light weight, large adsorption capacity and high selective adsorption, features that render it ideal as a high-performance sorbent for water treatment. The objective of this research was to develop novel hydrophobic polymer-reinforced silica aerogel microspheres (RSAMs) with water glass as the precursor, aminopropyltriethoxysilane as the modifier, and styrene as the crosslinker for oil removal from water. The effects of drying method and polymerization time on the structure and oil adsorption capacity were investigated. The drying method influenced the microstructure and pore structure in a noteworthy manner, and it also significantly depended on the polymerization time. More crosslinking time led to more volume shrinkage, thus resulting in a larger apparent density, lower pore volume, narrower pore size distribution and more compact network. Notably, the hydrophobicity increased with the increase in crosslinking time. After polymerization for 24 h, the RSAMs possessed the highest water contact angle of 126°. Owing to their excellent hydrophobicity, the RSAMs via supercritical CO₂ drying exhibited significant oil and organic liquid adsorption capabilities ranging from 6.3 to 18.6 g/g, higher than their state-of-the-art counterparts. Moreover, their robust mechanical properties ensured excellent reusability and recyclability, allowing for multiple adsorption–desorption cycles without significant degradation in performance. The novel sorbent preparation method is facile and inspiring, and the resulting RSAMs are exceptional in capacity, efficiency, stability and regenerability. Full article

Regarding the preparation of aerogels by the co-precursor method, the skeleton collapse caused by its low strength is one of the key problems that needs to be solved urgently. In this study, vinyl-functionalized silica aerogel was prepared under atmospheric drying conditions (APD) with vinyltriethoxysilane (V) and water glass (W) as co-precursors. The performance of aerogels varied with the components of co-precursors. When the V:W ratio was 0.8, the aerogel had excellent properties of low thermal conductivity (0.0254 W/(m·K)), super hydrophobicity (hydrophobic angle of 160°), high specific surface area (890.76 m²/g), high porosity (96.82%), and low density (0.087 g/cm³). Test results of SEM and BET showed that the V:W ratio affected the pore structure. When the V:W ratio was around 0.8, the aerogel had a dual modal pore structure composed of both small (6–8 nm) and large (20–30 nm) mesopores, which could contribute to enhance the skeleton strength of the aerogel. On the other hand, the addition of vinyltriethoxysilane promoted the skeleton stability by reducing the capillary force. The vinyltriethoxysilane and water glass as novel co-precursor combinations can provide guidance for the preparation of aerogels under APD conditions. Full article

This paper presents the use of hydrophobic silica aerogel (HSA) and hydrophilic fly ash cenosphere (FCS) aggregates for improvements in the thermal insulating and mechanical properties of 100- and 250 °C-autoclaved calcium aluminate phosphate (CaP) cement composites reinforced with micro-glass (MGF) and micro-carbon (MCF) fibers for deployment in medium- (100 °C) and high-temperature (250 °C) reservoir thermal energy storage systems. The following six factors were assessed: (1) Hydrothermal stability of HSA; (2) Pozzolanic activity of the two aggregates and MGF in an alkali cement environment; (3) CaP cement slurry heat release during hydration and chemical reactions; (4) Composite phase compositions and phase transitions; (5) Mechanical behavior; (6) Thermal shock (TS) resistance at temperature gradients of 150 and 225 °C. The results showed that hydrophobic trimethylsilyl groups in trimethylsiloxy-linked silica aerogel structure were susceptible to hydrothermal degradation at 250 °C. This degradation was followed by pozzolanic reactions (PR) of HSA, its dissolution, and the formation of a porous microstructure that caused a major loss in the compressive strength of the composites at 250 °C. The pozzolanic activities of FCS and MGF were moderate, and they offered improved interfacial bonding at cement-FCS and cement-MGF joints through a bridging effect by PR products. Despite the PR of MGF, both MGF and MCF played an essential role in minimizing the considerable losses in compressive strength, particularly in toughness, engendered by incorporating weak HSA. As a result, a FCS/HSA ratio of 90/10 in the CaP composite system was identified as the most effective hybrid insulating aggregate composition, with a persistent compressive strength of more than 7 MPa after three TS tests at a 150 °C temperature gradient. This composite displayed thermal conductivity of 0.28 and 0.35 W/mK after TS with 225 and 150 °C thermal gradients, respectively. These values, below the TC of water (TC water = 0.6 W/mK), were measured under water-saturated conditions for applications in underground reservoirs. However, considering the hydrothermal disintegration of HSA at 250 °C, these CaP composites have potential applications for use in thermally insulating, thermal shock-resistant well cement in a mid-temperature range (100 to 175 °C) reservoir thermal energy storage system. Full article

We report an experimental study on the gain of the Raman signal of aqueous mixtures and liquid water when confined in aerogel-lined capillaries of various lengths of up to 20 cm and various internal diameters between 530 and 1000 µm. The lining was made of hydrophobised silica aerogel, and the carrier capillary body consisted of fused silica or borosilicate glass. Compared to the Raman signal detected from bulk liquid water with the same Raman probe, a Raman signal 27 times as large was detected when the liquid water was confined in a 20 cm-long capillary with an internal diameter of 700 µm. In comparison with silver-lined capillaries of the same length and same internal diameter, the aerogel-lined capillaries featured a superior Raman signal gain and a longer gain stability when exposed to mixtures of water, sugar, ethanol and acetic acid. Full article

A spherical silica aerogel powder with hydrophobic surfaces displaying a water contact angle of 147° was synthesized from a water glass-in-hexane emulsion through ambient pressure drying. Water glass droplets containing acetic acid and ethyl alcohol were stabilized in n-hexane with a surfactant. Gelation was performed by heating the droplets, followed by solvent exchange and surface modification using a hexamethyldisilazane (HMDS)/n-hexane solution. The pH of the silicic acid solution was crucial in obtaining a highly porous silica aerogel powder with a spherical morphology. The thermal conductivity, tapped density, pore volume, and BET surface area of the silica aerogel powder were 22.4 mW·m⁻¹K⁻¹, 0.07 g·cm⁻³, 4.64 cm³·g⁻¹, and 989 m²·g⁻¹, respectively. Fourier transform infrared (FT–IR) spectroscopy analysis showed that the silica granule surface was modified by Si-CH₃ groups, producing a hydrophobic aerogel. Full article

The article presents the synthesis of silica aerogel from a much cheaper precursor of water glass that was reinforced with short pitch carbon fiber by way of ambient pressure drying. Before being added to the silica gel, the carbon fibers were surface modified to increase adhesion at the interfacial border. We were able to obtain stable structures of the composite with the amount of fibers above 10% by volume. The presence of fibers in the silica matrix resulted in lower synthesis time of the composite, improved adhesion of fibers to the aerogel nanostructure, and increased mechanical and structural parameters. An additional effect of the presence of fibers in excess of 10% by volume was a new function of the nanocomposite—the ability to conduct electric current. The most optimal parameters of the composite, however, were obtained for silica aerogel reinforced with 10 vol.% of carbon fibers. This material indicated relatively low density and good physical parameters. The paper also analyzes the results on the synthesis of fiber-reinforced silica aerogels that have appeared in recent years and compares these to the results gained in presented work. Full article

Silica aerogels have attracted much attention owing to their excellent thermal insulation properties. However, the conventional synthesis of silica aerogels involves the use of expensive and toxic alkoxide precursors and surface modifiers such as trimethylchlorosilane. In this study, cost-effective water-glass silica aerogels were synthesized using an eco-friendly catechol derivative surface modifier instead of trimethylchlorosilane. Polydopamine was introduced to increase adhesion to the SiO₂ surface. The addition of 4-tert-butyl catechol and hexylamine imparted hydrophobicity to the surface and suppressed the polymerization of the polydopamine. After an ambient pressure drying process, catechol-modified aerogel exhibited a specific surface area of 377 m²/g and an average pore diameter of approximately 21 nm. To investigate their thermal conductivities, glass wool sheets were impregnated with catechol-modified aerogel. The thermal conductivity was 40.4 mWm⁻¹K⁻¹, which is lower than that of xerogel at 48.7 mWm⁻¹K⁻¹. Thus, by precisely controlling the catechol coating in the mesoporous framework, an eco-friendly synthetic method for aerogel preparation is proposed. Full article

Ultra-high exfoliation in water of a nanosized graphite (HSAG) was obtained thanks to the synergy between a graphene layer edge functionalized with hydroxy groups and a polymer such as chitosan (CS). The edge functionalization of graphene layers was performed with a serinol derivative containing a pyrrole ring, serinol pyrrole (SP). The adduct between CS and HSAG functionalized with SP was formed simply with a mortar and pestle, then preparing water dispersions stable for months in the presence of acetic acid. Simple casting of such dispersions on a glass support led to carbon papers. Aerogels were prepared through the freeze-dry procedure. Exfoliation was observed in both these families of composites and ultra-high exfoliation was documented in aerogels swollen in water. Carbon papers and aerogels were stable for months in solvents in a wide range of solubility parameter and in a pretty wide range of pH. By considering that a moderately functionalized nanographite was straightforwardly exfoliated in water in the presence of one of the most abundant biobased polymers, the obtained results pave the way for the simple and sustainable preparation of graphene-based nanocomposites. HSAG–SP/CS adducts were characterized by wide angle X-ray diffraction (WAXD), scanning and transmission electron microscopy (SEM, TEM and HRTEM), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. Thermal stability of the composites was studied by thermogravimetric analysis (TGA) and their direct electrical conductivity with the four-point probe method. Full article

Sets of silica gels: aerogels, xerogels and sintered aerogels, have been studied in the objective to understand the mechanical behavior of these highly porous solids. The mechanical behaviour of gels is described in terms of elastic and brittle materials, like glasses or ceramics. The magnitude of the elastic and rupture modulus is several orders of magnitude lower compared to dense glass. The mechanical behaviours (elastic and brittle) are related to the same kinds of gel characteristics: pore volume, silanol content and pore size. Elastic modulus depends strongly on the volume fraction of pores and on the condensation reaction between silanols. Concerning the brittleness features: rupture modulus and toughness, it is shown that pores size plays an important role. Pores can be considered as flaws in the terms of fracture mechanics and the flaw size is related to the pore size. Weibull’s theory is used to show the statistical nature of flaw. Moreover, stress corrosion behaviour is studied as a function of environmental conditions (water and alcoholic atmosphere) and temperature. Full article