Silica Composites Research Articles

Methane Valorization through Direct Conversion to Methanol Using Catalysts Based on Copper-Modified Natural Clays

Introduction: A series of Cu-montmorillonite clay composites (MtCs), prepared through cation exchange and wet impregnation with varying amounts of copper, have been tested for the direct oxidation of methane to methanol. Methods: The catalysts were characterized using several analytical techniques, including surface area BET, X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Ammonia Temperature-Programmed Desorption (NH3-TPD), and pyridine desorption, followed by Fourier Transform Infrared (FTIR) spectroscopy. Catalytic tests were conducted at various temperatures and pressures using hydrogen peroxide as the oxidizing agent. Results: The characterization results indicated the incorporation of copper species to not significantly modify the clay composite morphology. The TEM images of the samples with low copper content (0.8 Cu wt.%) showed the copper particles to be uniformly distributed. Conversely, for the higher copper content samples (3.5 Cu wt.%) prepared by wet impregnation, the copper particles distributed around the montmorillonite clay composites. It has been observed that silica (MtC-Si) and aluminum (MtC-SiAl) montmorillonite clay composites have exhibited notable differences in acid site strength and distribution, influencing the dispersion and type of copper species being active for direct oxidation of methane to methanol. Conclusion: The findings have indicated the well-dispersed copper species, favored by the structure MtCs, to resulted in enhanced catalytic activity for methane’s oxidation to methanol.

Utilization of Silica from Palm Ash Waste as an Abrasive Material in Brake Friction Composite

The silica element in palm ash has the potential to be an alternative source of silica material to replace mineral silica, making it more environmentally friendly and reducing production costs. This research aims to utilize silica from palm ash waste as an abrasive material in brake friction composites. The silica from palm ash was isolated by a leaching process using 1 M HCl solution at a temperature of 70 °C for 90 minutes. Isolated silica was then characterized by X-ray fluorescence (XRF). The composition of silica was varied by volume fraction (0, 2, 4, and 6%). The mixing process of the powder mixture was conducted using a chopper mixer for 5 minutes, The powder mixture is then hot compressed using uniaxial hot pressing at a pressure of 47 MPa and a temperature of 165 °C for 15 minutes. Post-curing of the samples was carried out at a temperature of 165 °C for 10 hours. The samples were characterized by density, porosity, hardness R-scale, friction coefficient, and specific wear rate. The research results showed that the palm ash was successfully purified with a silica content of 27.3% to 57.2%. Increasing volume fraction of palm ash silica decreases in density and hardness, while porosity increases. The sample with 4% volume of palm ash silica exhibited better friction performance and a lower specific wear rate. Palm ash silica has the potential to replace the silica mineral for brake friction composites.

Hybrid Alumina-Silica Filler for Thermally Conductive Epoxidized Natural Rubber.

Thermally conductive composites were prepared based on epoxidized natural rubber (ENR) filled with alumina, silica, and hybrid alumina and silica. The thermal conductivity and mechanical properties were assessed. It was observed that the interactions of polar functional groups in the fillers and epoxy group in ENR supported a fine dispersion of filler in the ENR matrix. The mechanical properties were improved with alumina, silica, and hybrid alumina/silica loadings. The ENR/Silica composite at 50 phr of silica provided the highest 60 shore A hardness, a maximum 100% modulus up to 0.37 MPa, and the highest tensile strength of 27.3 MPa, while ENR/Alumina with 50 phr alumina gave the best thermal conductivity. The hybrid alumina/silica filler at 25/25 phr significantly improved the mechanical properties and thermal conductivity in an ENR composite. That is, the thermal conductivity of the ENR/Hybrid filler was 2.23 W/mK, much higher than that of gum ENR (1.16 W/mK). The experimental results were further analyzed using ANOVA and it was found that the ENR/Hybrid filler showed significant increases in mechanical and thermal properties compared to gum ENR. Moreover, silica in the hybrid composites contributed to higher strength when compared to both gum ENR and ENR/Alumina composites. The hybrid filler system also favors process ability with energy savings. As a result, ENR filled with hybrid alumina/silica is an alternative thermally conductive elastomeric material to expensive silicone rubber, and it could have commercial applications in the fabrication of electronic devices, solar energy conversion, rechargeable batteries, and sensors.

Selective diesterase-like activity of bioinspired FeIIINiII and FeIIIZnII complexes and their 3-aminopropyl silica composites: A homo- and heterogeneous catalytic study

In this study, the preparation and characterization of two new mixed-valence heterodinuclear complexes [FeIIINiII(BPPAMFF)(μ-OAc)2(H2O)]ClO4 (1) and [FeIIIZnII(BPPAMFF)(μ-OAc)2(H2O)]ClO4 (2) with the bioinspired ligand 2-[(N-benzyl-N-2-pyridylmethylamine)]-4-methyl-6-[N-(2-pyridylmethyl)aminomethyl)])-4-methyl-6-formylphenol (H2BPPAMFF) are reported. These compounds were immobilized in 3-aminopropyl silica (APS) to afford composites APS-1 and APS-2 successfully. The aldehyde-containing ligand provided a reactive functional group, which could serve as a cross-linking group to bind the complexes to the directly amino-modified SiO2 surface. The complexes’ chemical integrity on the APS inorganic platform were probed by spectroscopical techniques, such as FTIR, UV–Vis and EPR. Potentiometric and spectrophotometric titrations allowed the chemical species present in solution to be rationalized, and identified which of them were potentially active in the hydrolytic cleavage of phosphodiester 2,4-BDNPP. Kinetic studies showed that FeIIINiII species (1 and APS-1) presented higher catalytic efficiency (E = kcat/KM) than FeIIIZnII species (2 and APS-2). Catalytic mechanisms were proposed based on a series of kinetic experiments, in which all the catalysts tested behaved as selective phosphodiesterases. In addition, it was also demonstrated that the hydrolase activity of the immobilized catalytic centers, APS-1 and APS-2, was better than the homogeneous processes, where second coordination sphere effects may be involved in directing and stabilizing the transition state.

FUNCTIONAL OPTICAL MATERIALS BASED ON AEROGELS

Sol-chemistry is an efficient physico-chemical method for the preparation of porous glassy or nanocrystalline materials with tailored electrical, thermal or optical properties. This paper focuses on the dependence preparation–structure-properties of hydrophobic silica aerogel granules, powders and composites with a potential application as optical materials. Using the technique of subcritical preparation of silica aerogel powders, multicolour emitting composites containing Eu(phen)2(NO3 )3 or Tb(phen)2(NO3 )3 nanocrystals are obtained and characterized with luminescence spectroscopy, quantum yield determination and texture measurements. A dependence of the luminescence quantum yield on the degree of hydrophobicity α of the silica aerogel powders is described.

The effect of burning on the dissolution behaviour and silicon and oxygen isotope composition of phytolith silica

The δ30Si and δ18O values of opal-A precipitated in plants (silica phytoliths) have been shown to be useful for paleoenvironmental reconstructions. Here, the effects of burning and partial dissolution of phytoliths on their isotopic compositions and dissolution behaviour were examined. Phytoliths were heated to 700 °C and then dissolution experiments were conducted in batch reactors under a range of pH (4–8) and temperature (4–19 °C) conditions. Heating caused a −2.6 ‰ shift in phytolith δ18O values. NMR results suggest that heating reduces the number of surface vicinal silanols, which likely results in the formation of strained SiOSi bonds which incorporate oxygen from 18O-depleted hydroxyl groups. During dissolution, the δ18O of burned phytoliths increased by up to 3.5 ‰ (average 1.8 ‰) until 15–45 % saturation was reached, and then adsorption of silica on the surface of the solid began to reduce the δ18O value of solid silica despite a net dissolution. The maximum increase in δ18O during dissolution of burned phytoliths is 1.8 ‰ smaller than previously observed for unburned silica subjected to partial dissolution under the same conditions. Heating did not cause a significant change in δ30Si values, and partial dissolution of burned phytoliths caused a slight increase in δ30Si values that was smaller in magnitude than for unburned phytoliths. Dissolution of burned phytoliths progressed more slowly than dissolution of fresh phytoliths in low pH and temperature conditions, but was faster than the dissolution of fresh phytoliths when pH > 6 and temperature = 19 °C. We propose that because fewer hydrolysis sites exist on the surface of burned phytoliths that the isolated silanols that remain after heating are difficult to deprotonate at low pH resulting in slower dissolution. However, at higher pH the breakage of strained SiOSi bonds in burned phytoliths may explain their higher dissolution rate relative to fresh phytoliths. We recommend caution in using the δ18O values of soil phytoliths in paleoclimate reconstructions as they can be altered during both heating and partial dissolution. For phytolith assemblages collected from archaeological hearths or grasslands prone to wildfires, the shift towards lower δ18O values caused by heating would result in overestimations of temperature using paleothermometer equations. Care must be taken to identify alteration by dissolution or burning, which may not always be visually evident.

Optimization of polishing fluid composition for single crystal silicon carbide by ultrasonic assisted chemical-mechanical polishing

Silicon carbide (SiC) is renowned for its exceptional hardness, thermal conductivity, chemical stability, and wear resistance. However, the existing process is difficult to meet the high standards of uniform corrosion in its polishing process and surface roughness and flatness after polishing, new polishing fluids and technique optimization are crucial for development. The study optimized and validated the composition of the polishing fluid used in ultrasonic-assisted chemical-mechanical polishing (UACMP). Abrasives significantly influenced the material removal rate (MRR) and surface roughness (Ra), contributing 67.63% and 56.43%, respectively. Organic bases and pH buffers significantly affected Ra, accounting for 19.66% and 21.44%, respectively. The optimum composition was determined, consisting of triethylamine (3wt%), potassium hydrogen phthalate (1wt%), a composite of silica and alumina abrasive particles (5wt%), and hydrogen peroxide (6wt%), which reduced the Ra from 95 nm to 3 nm. The MRR achieved 25.96 nm/min. In comparison to the 7 nm minimum roughness from the orthogonal test, the optimal scheme’s Ra was reduced by 57.14%, leading to a significant enhancement in overall surface quality. In this paper, a new type of additive is added to prepare the polishing liquid, which provides a new idea for the UACMP of SiC and has a great impact.

Highly efficient green-synthesized sucrose-derived graphene silica and carbonate sand composites for copper (II) ions removal

Highly efficient green-synthesized sucrose-derived graphene silica and carbonate sand composites for copper (II) ions removal

ZnO Impregnated Graphene Silica Composite to Enhance Cr(VI) Adsorption: Batch Studies

Abstract Hexavalent chromium [Cr(VI)] is a profoundly poisonous heavy metal due to its significant mobility across cell membranes as HCrO4 − and CrO4 2- ions. There is a limited amount of research on the effectiveness of metal oxide impregnated graphene silica composite (GSC) as adsorbents for treating [Cr(VI)]. However, the existing studies indicate that these composites are very efficient. The project involved synthesizing a new type of adsorbent by impregnating zinc oxide (ZnO) particles onto a composite material of graphene and silica. This was achieved using the co-precipitation method. The findings revealed that the highest level of Cr (VI) removal (97%) is achieved at basic, a contact period of 45 minutes. The Langmuir isotherm had the highest degree of fit, suggesting a uniform and chemical adsorption process with the highest possible adsorption capacity of 142 mg/g. The application of ZnO on GSC improves the motion of Cr(VI) in the composite, resulting in an increase in both the adsorption capacity and adsorption kinetics. The findings of this investigation show that the ZnO/GSC composite is a very effective and versatile adsorbent for treating wastewater, highlighting its new and reusable properties.

Determination of adsorption capacity, regeneration ability, and aggregation tendency toward inorganic and organic pollutants of metal-doped carbon–silica composites in multicomponent systems

Abstract The main aim of the study was to develop a method for determining the adsorption capacity, regeneration ability, and aggregation tendency of metal-doped carbon–silica composites (iron-doped, C/Fe/SiO2, and manganese-doped, C/Mn/SiO2) against heavy metals and selected organic substances. The properties of these composites were compared with those of metal-free silica–carbon composite (C/SiO2). Inductively coupled plasma–optical emission spectrometry (ICP–OES) and high-pressure liquid chromatography were used to determine the adsorbed amounts and the desorption degree of organic/inorganic pollutants. Potentiometric titrations and electrophoretic mobility measurements were conducted to understand the mechanisms that were driving adsorption and particle aggregation. The size of the aggregates formed in the systems as well as the stability of the examined suspension were estimated by using ultraviolet-visible spectrophotometry. The performed experiments showed that the selected combination of methods is appropriate to determine the potential of metal-doped carbon–silica composites as adsorbents as well as the ease of their removal with adsorbed contaminants from aqueous solutions by sedimentation.

Development of multi-layered three-dimensional printed scaffold for sequential delivery of biomolecules

Spatiotemporal control of exogenous growth factors plays a crucial role in the sequential repair of damaged tissues. However, traditional therapeutic trials have mostly relied on the delivery of a single molecule because of the limitations of rapid diffusion and the instability of biomolecules. In this study, we developed a novel strategy using a composite of gelatin and silica as an alternative for the stable and sequential release of biomolecules. Two biomolecules, basic fibroblast growth factor and bone morphogenetic protein-2, were incorporated into two separate composites and sequentially layered onto the activated polymer surface. Each molecule was sequentially released from each layer of the scaffold and the silica composite prevented rapid diffusion owing to its nano-porous structure. The adhesion, proliferation, and osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells were significantly enhanced in the double-layered group containing separately delivered dual molecules compared with the control or single groups. Our developed gelatin–silica composite was successfully placed in double layers on polymer scaffolds, and cellular responses were promoted in this manner. These results demonstrated that our scaffolding system has potential as a therapeutic strategy for the delivery of dual or multiple biomolecules in regenerative medicine.  

Preparation of High-Temperature Resistant Aerogels by Incorporating Aluminum Sol into Composite Silica Sources Using Ambient Pressure Drying.

To reduce production costs and enhance the high-temperature resistance of SiO2 aerogels, an aluminum-doped silica aerogel (ASA) was successfully prepared using the sol-gel method and atmospheric drying method. The composite silica sources included TEOS and inexpensive acidic silica sol, while the aluminum source was aluminum sol. The study investigated the influence of the molar ratio of acidic silica sol to TEOS, Al/Si, and calcination temperature on the composition, structure, and high-temperature resistance of the ASA. The results indicate that a sample with an acidic silica sol to TEOS molar ratio of 0.8 achieved a specific surface area of 683.204 m2·g-1. The Al/Si molar ratio significantly impacted the high-temperature resistance of the ASA, with the sample having a molar ratio of 0.02 Al/Si displaying the highest specific surface area of 705.956 m2·g-1 at 600 °C. Moreover, this surface area remained at 273.099 m2·g-1 after calcination at 1000 °C, notably higher than the sample without aluminum sol (16.082 m2·g-1). Mechanism analysis indicated that the addition of aluminum sol to the SiO2 aerogel inhibited phase transitions, and both acidic silica sol and aluminum sol particles enhanced the aerogel structure, contributing to a marked improvement in high-temperature resistance.

Composite silica aerogel based on HNTs-modified APP with enhanced thermal insulation and flame retardancy performance for organosilicon resin

Efficient thermal insulation and flame-retardant materials are crucial in reducing energy consumption and minimizing fire hazards. This work presents a novel method for preparing a composite aerogel: a silane coupling agent was used as a chemical bridge to synthesize a new flame retardant AKH (modified APP with HNTs). AKH was incorporated into the silica sol to fabricate the SA-AKH composite aerogel. SA-AKH features a dense three-dimensional network skeletal structure, excellent thermal stability, and a high specific surface area. When integrated into organosilicon resin, SA-AKH significantly enhances the flame resistance of composite materials. During cone calorimetry testing (CCT), SSAKH4 exhibited a peak heat release rate (PHRR) of 281.88 kW/m2 and total smoke production (TSP) of 5.52 m2, representing a decrease of 30.8 % and 4.5 %, respectively, compared to SSA4. The composite material, derived from the unique mesoporous structure of aerogel combined with the flame retardant and hollow characterization of AKH, demonstrates exceptional flame retardancy and smoke suppression. SA-AKH is expected to make novel advancements in the field of high-efficiency insulation and flame-resistant composites.

Cost-effective preparation of pre-oxygenated PAN fiber composite SiO2 aerogel felt with excellent mechanical and thermal insulation properties

Silica aerogel is an attractive thermal insulation material due to its low thermal conductivity, light weight and non-combustible inorganic properties, but its inherent brittleness and high production cost hinder its practical application on a large scale. Herein, the high-performance pre-oxidized polyacrylonitrile fiber composite silica aerogel felt (PPAF-SiO2) was successfully prepared by a cost-effective combustion drying technique for the first time. The results show that the PPAF-SiO2 has the feature of lightweight, good flexibility, and its heat resistance, hydrophobicity, and specific surface area are significantly improved. Due to the further polymerization of fiber structure molecules caused by combustion, the tensile strength of the PPAF-SiO2 is increased by 81.9 % to 1.71 MPa. More importantly, due to the high proportion of silica aerogel in felt, its thermal conductivity can be reduced to 0.02 W/(m·K), which is lower than most aerogel composite materials. Moreover, the thermal insulation performance of the PPAF-SiO2 was further confirmed by the infrared thermal imager from room temperature to 300 ℃. In addition, the innovative drying mechanism based on the combustion flame model was proposed. Finally, compared with traditional physical drying technologies in terms of drying time and drying conditions, the combustion drying technology shows great advantages in drying efficiency, energy consumption and equipment investment, which greatly reduces production costs. The combustion drying technology opens up a promisingly method for high efficiency, low energy consumption, and low cost preparation of silica aerogel composites.

The performance of CO2 reduction by dielectric barrier discharge plasma coupled Cu-Ni binary silicon-based composites

As a major greenhouse gas, the rational conversion and utilization of CO2 can help reduce carbon emissions and mitigate the greenhouse effect. In this study, mesoporous SiO2 as a carrier, with CuO and NiO employed to construct a binary metal composite silica-based catalyst, coupled with dielectric barrier discharge (DBD) plasma, for the conversion of CO2. Physicochemical analysis confirmed the successful introduction of CuO into the mesoporous SiO2. NiO and CuO bimetals were dispersed on SiO2 surfaces with large specific surface areas, ensuring an optimal distribution of metal oxide. Gas chromatography was utilized to investigate the performance of DBD-coupled x%CuO-3 %NiO/Si for CO2 conversion. The results indicated that the CuO-NiO binary composite silica catalysts significantly improved CO2 conversion, CO yield, and energy efficiency compared to the monometallic 3 %NiO/Si materials. Further microstructural analysis of the 9 %CuO-3 %NiO/Si catalyst revealed near-elliptic particles with dimensions of 200 by 500 nm and a large number of irregular fine particles attached to the surface. When the CuO loading reached an optimal level and the input power was set at 30 W, the energy efficiency of the 9 %CuO-3 %NiO/Si catalyst increased by 119.6 %. The CuO-NiO binary composite Si-based catalyst developed in this study boasts simple operation and environmental friendliness, making it highly significant for CO2 treatment.

Hierarchical Silica Composites for Enhanced Water Adsorption at Low Humidity.

To combat water scarcity in remote areas around the world, adsorption-based atmospheric water harvesting (AWH) has been proposed as a technology that can be used alongside existing water production capabilities. However, commonly used adsorbents either have low water adsorption loadings or are difficult to regenerate. In this work, we developed two novel hierarchical silica-salt composites that both exhibit high water adsorption loadings under dry and humid conditions. The total water vapor loading, kinetics, and heats of water adsorption for both silica-salt composites were investigated. As hierarchical silicas have tunable pores and large pore volumes, these materials serve as effective host matrixes for the hygroscopic salt LiCl. Our results suggest that hierarchical pores play a significant role in water adsorption: micropores and some smaller mesopores act as "storage" sites for hygroscopic salt, whereas larger mesopores and macropores increase the accessibility of water vapor into the silica. Using this mix of pores, we achieved greater than 0.4 g H2O/g composite at 10% RH and 27 °C. Additionally, we found that the salt-impregnated silica and bare silica had the same heat of adsorption: 80-90 kJ/mol. The results suggest that the H-bond interactions are similar for both systems and that the primary mechanism at play here is water cluster adsorption/desorption. Despite the similar energies, the LiCl-containing materials exhibited considerably slower kinetics than bare silica materials. Of equal importance to the adsorption capacity and kinetics of these composites is their mechanical stability. To assess their mechanical stability, high-energy ball milling of silica was conducted to create more uniform particle sizes. However, reduced particle sizes came at a cost─the BET surface areas and pore volumes were drastically decreased after more than 1 h of ball milling. Findings from this study suggest that short-term ball milling may be a viable large-scale option to reduce particle size in silica materials without sacrificing significant performance.

Vibration isolation performance of silica aerogel blankets and boards, fumed silica, polymer aerogel and nanofoams

Buildings are often constructed on a continuous layer of vibration isolation to reduce vibrations and structure-borne noise. There are many vibration isolation products (rubber mats, textiles, polymer foams), but none fulfils all requirements in terms of load-bearing capacity, performance, and cost. In previous work, we have shown that silica aerogel particle beds display a low resonance frequency and correspondingly high vibration isolation performance. Loose silica aerogel granules are not a practical vibration isolation solution. In order to guide the future development of dedicated vibration isolation products based on aerogels, we determine the vibro-acoustic properties of a variety of existing commercial and R&D stage mesoporous composites, that have been developed for thermal insulation applications. The sample set includes monolithic aerogels (polyurethane), silica aerogel composites (aerogel – fibers, aerogel impregnated foams, aerogel bound with polymer foam), glued fumed silica-fiber boards, and nanoporous polymer foam composite boards. The silica aerogel and fumed silica composites display low resonance frequencies (down to 8 Hz for 40 mm, strongly dependent on composite type) and a low dynamic stiffness and loss factor over a wide range of static loads. The polymer aerogel, nanoporous foam and polymer-bound silica aerogel granule board all display higher resonance frequencies, consistent with their higher static stiffness. Although optimized for thermal insulation rather than vibration isolation, many of the tested silica aerogel and fumed silica composites are competitive with the best vibration isolation products on the market in terms of vibration isolation performance. The diversity of materials tested informs on which approaches, materials, and materials combinations are most promising to target vibration isolation.

Duo photoprotective effect via silica-coated zinc oxide nanoparticles and Vitamin C nanovesicles composites

ObjectiveZinc Oxide nanoparticles (ZnO NPs) are used widely in nowadays personal care products, especially sunscreens, as a protector against UV irradiation. Yet, they have some reports of potential toxicity. Silica is widely used to cage ZnO NPs to reduce their potential toxicity. Vitamin C derivative, Magnesium Ascorpyl Phosphate (MAP), is a potent antioxidant that can efficiently protect human skin from harmful impacts of UV irradiation and oxidative stress. The combination of silica coated ZnO NPs and MAP nanovesicles could have potential synergistic protective effect against skin photodamage.MethodsSilica coated ZnO NPs and MAP nanovesicles (ethosomes and niosomes) were synthesized, formulated, and evaluated as topical gels. These gel formulations were evaluated in mice for their photoprotective effect against UV irradiation through histopathology and immuno-histochemistry study. Split-face clinical study was conducted to compare the effect of application of silica coated ZnO NPs either alone or combined with MAP nanovesicles. Their photoprotective action was evaluated, using Antera 3D® camera, for melanin level, roughness index and wrinkles depth.ResultsSilica coated ZnO NPs when combined with MAP nanovesicles protected mice skin from UV irradiation and decreased the expression of the proinflammatory cytokines, NF-κB. Clinically, silica coated ZnO NPs, alone or combined with MAP nanovesicles, could have significant effect to decrease melanin level, roughness index and wrinkles depth with higher effect for the combination.ConclusionA composite of silica coated ZnO NPs and MAP nanovesicles could be a promising cosmetic formulation for skin protection against photodamage signs such as hyperpigmentation, roughness, and wrinkles.Graphical

Research on the influence of microsilica on the strength of concrete used in the composition of a two-component modified additive

In modern construction, considerable attention is paid to the search for environmentally safe and cost-effective methods to improve the performance of concrete. This paper investigates the potential of a complex admixture developed on the basis of industrial wastes, in particular microsilica, phosphogypsum, soapstock and post-alcoholic bard for concrete modification. The aim of the study is to evaluate the effect of each component of the admixture on the transformation processes of concrete, especially on its strength characteristics. Laboratory tests were carried out on specimens with different microsilica content and the results showed that the maximum strength increase was achieved at a microsilica content of 20 % in relation to the cement mass. Further analysis revealed a decrease in strength performance when the microsilica content increased above 20 %, which may be due to the overabundance of silica in the binder composition.

Dual role of two-dimensional graphene in silica aerogel composite: Thermal resistance and heat node

Incorporating two-dimensional graphene sheets, known for their high in-plane thermal conductivity, into silica aerogel enhances both the thermal insulation and mechanical properties of the composite. This work delves into the impact of graphene doping on the solid thermal conductivity of silica composites and their mechanical characteristics, employing molecular dynamics simulations that encompass both amorphous silica bulk and porous silica aerogel structures. Our findings reveal that graphene–silica interface thermal resistance notably restricts heat conduction in graphene doped silica aerogel, with the most pronounced effect occurring when graphene aligns vertically with the heat flux. Within porous silica aerogel, graphene serves as a “heat node”, bridging and connecting adjacent pores. A notable “trade-off” emerges: high weight percentages of graphene sheets augment heat transfer through the “heat node effect”, whereas the interfacial thermal resistance between graphene and aerogel reduces solid heat transfer, leading to decreased thermal conductivity. Additionally, while the inclusion of graphene sheets offers limited mechanical property enhancements, their two-dimensional structure can cause detachment and slipping from the silica matrix, leading to localized improvements in mechanical strength. This work sets the stage for advancing graphene-based aerogel composites characterized by low thermal conductivity and enhanced mechanical properties.