Search Results (11)

A huge challenge is how to prepare flexible silicone aerogel materials with good flame retardancy, thermal stability, and hydrophobic properties. In this paper, resorcinol–formaldehyde was introduced into the silicone network composed of methyltrimethoxysilane (MTMS), phenyltriethoxysilane (PTES), and dimethyldimethoxysilane (DMDMS). Flexible hybrid aerogels with excellent thermal insulation, flame retardant, and hydrophobic properties were prepared by the sol–gel method and ambient pressure drying (APD), and the preparation process does not require long-term solvent exchange, only about 3 h of soaking and washing of the wet gel. The results show that the prepared phenolic-silicone aerogel has low density (0.093 g/cm³), low thermal conductivity (0.041 W/m·K), high flexibility, and compression fatigue resistance. The phenolic microspheres are bonded to the silicone skeleton to maintain the original flexibility. After 50% compression deformation, it returns to the original size normally, and there is no significant change in the stress of the sample after 50 compression cycles. Compared with pure silicone aerogels, the hybrid aerogels doped with phenolic have better char yield (65.28%) and higher decomposition temperature (609 °C). The hybrid aerogel sample has good flame-retardant properties, which can withstand alcohol lamp burning without being ignited. The micron-sized phenolic beads give the hybrid aerogels better hydrophobic properties, showing a higher static water contact angle (152°). The excellent thermal and mechanical properties mean that the hybrid aerogels prepared in this paper have good application prospects for aerospace, outdoor equipment, and other fields. Full article

Gels, specifically hydrogels and aerogels, have emerged as versatile materials with profound implications in pharmaceutical sciences. This comprehensive review looks into detail at hydrogels and aerogels, providing a general introduction to gels as a foundation. The paper is then divided into distinct sections for hydrogels and aerogels, each delving into their unique formulations, advantages, disadvantages, and applications. In the realm of hydrogels, we scrutinize the intricacies of formulation, highlighting the versatile advantages they offer. Conversely, potential limitations are explored, paving the way for a detailed discussion on their applications, with a specific focus on their role in antimicrobial applications. Shifting focus to aerogels, a thorough overview is presented, followed by a detailed explanation of the complex formulation process involving sol–gel chemistry; aging; solvent exchange; and drying techniques, including freeze drying, supercritical drying, and ambient-pressure drying (APD). The intricacies of drug loading and release from aerogels are addressed, providing insights into their pharmaceutical potential. The advantages and disadvantages of aerogels are examined, accompanied by an exploration of their applications, with a specific emphasis on antimicrobial uses. The review culminates in a comparative analysis, juxtaposing the advantages and disadvantages of hydrogels and aerogels. Furthermore, the current research and development trends in the applications of these gels in pharmaceutical sciences are discussed, providing a holistic view of their potential and impact. This review serves as a comprehensive guide for researchers, practitioners, and enthusiasts, seeking a deeper understanding of the distinctive attributes and applications of hydrogels and aerogels in the ever-evolving research concerning pharmaceutical sciences. Full article

An ever-increasing number of applications of oxide aerogels places a high demand on wettability-tuning techniques. This work explores the possibility to cheaply prepare GeO₂ aerogels with controlled wettability by an ambient pressure drying (APD) method. GeO₂ aerogels are prepared via two synthetic routes. Surface modification is carried out by soaking the gels in a silylating agent solution; type and concentration of the modifier are optimized to achieve a large surface area. The aerogels have been characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, nitrogen adsorption and contact angle measurements. The effect of surface modification on the phase composition and particle size of the aerogels is described. In summary, the work provides a new cheap production method for the preparation of both hydrophobic and hydrophilic GeO₂ aerogels with contact angle varying from 30° to 141° and with surface area of 90–140 m²/g, which facilitates the expansion of their diverse applications. GeO₂ aerogel synthesis by APD is reported for the first time. Full article

Ambient pressure drying (APD) of silica aerogels has emerged as an attractive method adapting to large-scale production. Spring-back is a unique phenomenon during APD of silica aerogels with volume expansion after its shrinkage under capillary force. We attribute the intense spring-back at elevated drying temperatures to a dense structure formed on the surface and the formation of positive internal pressure. Furthermore, an APD-assisted foaming method with an in situ introduction of NH₄HCO₃ was proposed. NH₄HCO₃ decomposing at drying temperatures hastened the emergence of positive pressure, thereby increasing the expansion volume. Compared to the previous method, the porosity of silica aerogel increased from 82.2% to 92.6%, and mesopore volume from 1.79 cm³ g⁻¹ to 4.54 cm³ g⁻¹. By adjusting the amount of the silicon source, silica aerogels prepared by the APD-assisted foaming method generated higher volume expansion and lower thermal conductivity. After calcination to remove undecomposed ammonium salts, the hydrophobic silica aerogel with a density of 0.112 g cm⁻³ reached a mesopore volume of 5.07 cm³ g⁻¹ and a thermal conductivity of 18.9 mW m⁻¹·K⁻¹. This strategy not only improves the thermal insulation properties, but also offers a significant advancement in tailoring silica aerogels with specific porosity and mesopore volume for various applications. Full article

This paper presents the effect of drying control agents on the physicochemical and thermal properties of hydrophobic silica aerogels derived via the ambient pressure drying (APD) method by a surface silylation using a TMCS/n-hexane mixture. The structural and physicochemical properties of synthesized DMF-modified and unmodified hydrophobic silica aerogels were characterized using Brunauer–Emmett–Teller (BET) analysis, thermo-gravimetric analysis, FT-IR, and Raman spectroscopic techniques. Based on the obtained results, the differences in structure between samples before and after a surface silylation and the effect of drying control agents were documented. The structural measurements confirmed the efficient silylation process (TMCS/n-hexane), as well as the presence of DMF residues of hydrogen bonded with unreacted Si-OH silanol groups within the silica backbone after surface modification. Based on TG analysis, it was found that DMF addition improves thermal resistance (up to 320 °C) and hydrophobic character of prepared aerogel. Modification of the silica aerogel synthesis process by DMF also resulted in a significant increase in BET—the specific surface area, for the unmodified aerogel was ~828 m²/g, and for the DMF-modified aerogel more than 1200 m²/g—much higher than the value of silica aerogels available on the market. Full article

Dye wastewater has caused great harm to the environment, which is an urgent problem to be solved. As typical three-dimensional porous materials, aerogels have attracted great interest in dye wastewater treatment. In this work, spherical attapulgite/silica (ATP/SiO₂) gels were initially prepared by easily scalable sol-gel dripping methods and then dried to aerogels with three drying techniques, namely, supercritical CO₂ drying (SCD), freeze-drying (FD), and ambient pressure drying (APD). The effect of the drying techniques and heat-treated temperature on the physical characteristic, morphological properties, microstructure, and chemical structure of the spherical ATP/SiO₂ aerogels were investigated. The macroscopic morphology of the spherical ATP/SiO₂ aerogels was homogeneous and integrated without local cracking. The average pore diameter and specific surface area of the spherical ATP/SiO₂ aerogels prepared by the three drying techniques were in the range of 6.8–8.6 nm and 218.5–267.4 m²/g, respectively. The heat treatment temperature had a significant effect on the pore structure and the wetting properties of the aerogels. The 600 °C heat-treated aerogels were subjected to adsorption tests in methylene blue (MB) solution (60 mg/g, 100 mL), which exhibited a great adsorption capacity of 102.50 mg/g. Therefore, the resulting spherical ATP/SiO₂ aerogels possessed multipath preparation and exhibited an efficient adsorption performance, with the potential to be applied as an adsorbent for dye wastewater. Full article

Composite hydrogels samples consisting of poly(methyl methacrylate/butyl acrylate/2-hydroxyethylmethacrylate) (poly-OH) and up to 60% reduced graphene oxide (rGO) containing rGO were synthesized. The method of coupled thermally induced self-assembly of graphene oxide (GO) platelets within a polymer matrix and in situ chemical reduction of GO was applied. The synthesized hydrogels were dried using the ambient pressure drying (APD) and freeze-drying (FD) methods. The effects of the weight fraction of rGO in the composites and the drying method on the textural, morphological, thermal, and rheological properties were examined for the dried samples. The obtained results indicate that APD leads to the formation of non-porous xerogels (X) of high bulk density (D), while FD results in the formation of highly porous aerogels (A) with low D. An increase in the weight fraction of rGO in the composite xerogels leads to an increase in D, specific surface area (SA), pore volume (Vp), average pore diameter (dp), and porosity (P). With an increase in the weight fraction of rGO in A-composites, the D values increase while the values of SP, Vp, dp, and P decrease. Thermo-degradation (TD) of both X and A composites takes place through three distinct steps: dehydration, decomposition of residual oxygen functional group, and polymer chain degradation. The thermal stabilities (TS) of the X-composites and X-rGO are higher than those of the A-composites and A-rGO. The values of the storage modulus (E’) and the loss modulus (E”) of the A-composites increase with the increase in their weight fraction of rGO. Full article

Ambient pressure drying (APD) can prospectively reduce the costs of aerogel fabrication and processing. APD relies solely on preventing shrinkage or making it reversible. The latter, i.e., the aerogel re-expansion after drying (so-called springback effect—SBE), needs to be controlled for reproducible aerogel fabrication by APD. This can be achieved by an appropriate surface functionalization of aerogel materials (e.g., SiO₂). This work addresses the fabrication of monolithic SiO₂ aerogels and xerogels by APD. The effect of several silylation agents, i.e., trimethylchlorosilane, triethylchlorosilane, and hexamethyldisilazane on the SBE is studied in detail, applying several complementary experimental techniques, allowing the evaluation of the macroscopic and microscopic morphology as well as the composition of SiO₂ aerogels. Here, we show that some physical properties, e.g., the bulk density, the macroscopic structure, and pore sizes/volumes, were significantly affected by the re-expansion. However, silylation did not necessarily lead to full re-expansion. Therefore, similarities in the molecular composition could not be equated to similarities in the SBE. The influences of steric hindrance and reactivity are discussed. The impact of silylation is crucial in tailoring the SBE and, as a result, the APD of monolithic aerogels. Full article

To further reduce the manufacturing cost and improve safety, silica aerogel composites (SAC) with low density and low thermal conductivity synthesized via ambient pressure drying (APD) technology have gradually become one of the most focused research areas. As a solvent, ethanol is flammable and needs to be replaced by other low surface tension solvents, which is dangerous and time-consuming. Therefore, the key steps of solvent replacement and surface modification in the APD process need to be simplified. Here, we demonstrate a facile strategy for preparing high strength mullite fiber reinforced SAC, which is synthesized by APD using water as a solvent, rather than using surface modification or solvent replacement. The effects of the fiber density on the physical properties, mechanical properties, and thermal conductivities of SAC are discussed in detail. The results show that when the fiber density of SAC is 0.24 g/cm³, the thermal conductivity at 1100 °C is 0.127 W/m·K, and the compressive strength at 10% strain is 1.348 MPa. Because of the simple synthesis process and excellent thermal-mechanical performance, the SAC is expected to be used as an efficient and economical insulation material. 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

Owing to their ultra-low thermal conductivity, silica aerogels are promising thermal insulators; however, their extensive application is limited by their high production cost. Thus, scientists have started to explore low-cost and easy preparation processes of silica aerogels. In this work, a low-cost method was proposed to prepare silica aerogels with industrial silica hydrosol and a subsequent ambient pressure drying (APD) process. Various surfactants (cationic, amphoteric, or anionic) were added to avoid solvent exchange and surface modification during the APD process. The effects of various surfactants on the microstructure, thermal conductivity, and thermal stability of the silica aerogels were studied. The results showed that the silica aerogels prepared with a cationic or anionic surfactant have better thermal stability than that prepared with an amphoteric surfactant. After being heated at 600 °C, the silica aerogel prepared with a cationic surfactant showed the highest specific surface area of 131 m²∙g⁻¹ and the lowest thermal conductivity of 0.038 W∙m⁻¹∙K⁻¹. The obtained low-cost silica aerogel with low thermal conductivity could be widely applied as a thermal insulator for building and industrial energy-saving applications. Full article