Effect of the loading amount and arrangement of iodine chains on the interfacial thermal transport of carbon nanotubes: a molecular dynamics study

Due to their excellent electrical and thermal conductivity properties, the nano-scale characteristics of carbon nanotubes (CNTs) are expected to be suitable for very large-scale integrated circuits and for next-generation micro interconnected devices. Consequently, CNT–metal composite materials have been widely researched, and have shown excellent performance in terms of thermal conductivity, electrical conductivity, thermal expansion, and adaptability to microelectronic devices. However, there are few studies on halogen–CNT composite materials with characteristics similar to CNT–metal composites, including regarding the remarkable electrical compatibility of the halogen and CNT and the large number of low-frequency phonons that are beneficial for thermal transport. In this work, iodine chains were considered to explore the halogen effect on CNTs. Variation of the interfacial thermal conductance of CNTs as a function of the iodine chains loading amount and arrangement was explored by a molecular dynamics method. The heat transfer mechanism was further analyzed based on the phonon state difference. This research is expected to provide a new pathway for the application of CNT composite materials in the field of next-generation microelectronics.

Study of the heat transfer enhancement mechanism of a CNTs'' interface by iodine particles loaded in different amounts and arrangements.     

Thermal conductivity and molecular heat transport of nanofluids

Fluid media such as water and ethylene glycol are usually quite poor conductors of heat. Nanoparticles can improve the thermal properties of fluids in a remarkable manner. Despite a plethora of experimental and theoretical studies, the underlying physics of heat transport in nanofluids is not yet well understood. Furthermore, the link between nanoscale energy transport and bulk properties of nanofluids is not fully established. This paper presents a thermal conductivity model, encapsulating solid–liquid interfacial thermal resistance, particle shape factor and the variation of thermal conductivity across a physisorbed fluidic layer on a nanoparticle surface. The developed model for thermal conductivity integrates the interfacial Kapitza resistance, the characteristics of a nanolayer, convective diffusion and surface energy with capillary condensation. In addition, the thickness of the nanolayer is predicted using the Brunauer–Emmett–Teller (BET) isotherms and micro/nano-menisci generated pressures of condensation. Such a comprehensive model for thermal conductivity of nanoparticles and systematic study has not hitherto been reported in the literature. The thermal conductivity model is evaluated using experimental data available in open literature.

The developed model for thermal conductivity of nanofluids integrates the interfacial Kapitza resistance, the characteristics of the nanolayer, convective diffusion and surface energy with capillary condensation.     

Ethylene glycol-based solar-thermal fluids dispersed with reduced graphene oxide

Direct absorption solar collectors, which use optical nanofluids to volumetrically absorb and convert sunlight into heat, have emerged as promising devices to harvest solar-thermal energy for many heat-related applications. Nanofluids, however, generally suffer from aggregation issues and the widely investigated water-based fluids only enable solar-thermal harvesting at relatively low temperatures. Herein, we report a facile way to prepare stably dispersed reduced graphene oxide-ethylene glycol (rGO-EG) fluids for solar-thermal energy harvesting at medium temperatures. Without the use of complex surface modification process, the homogeneous dispersion of rGO-EG fluids was achieved by utilizing the favorable interaction between the oxygen-containing groups on the rGO surfaces and EG molecules. The rGO-EG fluids were prepared by reducing the GO-EG fluids that are uniformly dispersed with ethanol-wetted GO through a single step of heating. The prepared rGO-EG fluids have suitable thermophysical properties for direct solar-thermal energy harvesting, such as broadband absorption of sunlight, high specific heat capacity and low viscosity. The rGO-EG fluids have shown stable uniform dispersion up to 120 °C and have demonstrated consistent solar-thermal energy harvesting performance during repeated solar radiation at ∼110 °C.

Ethylene glycol nanofluids uniformly dispersed with reduced graphene oxide were prepared for medium-temperature direct absorption-based solar-thermal energy harvesting.     

Largely enhanced thermal conductivity and thermal stability of ultra high molecular weight polyethylene composites via BN/CNT synergy

In recent years, thermally conductive polymer-based composites have garnered significant attention due to their light weight and easy formation process. In this work, the thermal conductivity of ultra high molecular weight polyethylene (UPE) composites was improved through construction of a hybrid filler network of boron nitride sheets (BNs) and carbon nanotubes (CNTs) in the matrix via hot compression. The morphology, UPE aggregate structure, thermal conductivity, heat dissipation capacity and thermal stability of the UPE composites were investigated. The thermal conduction mechanism of the UPE composites was explored through simulations with Agari''s semi-empirical formula. The results showed that the thermal conductivity of the UPE composite with 40 wt% BNs and 7 wt% CNTs was 2.38 W m⁻¹ K⁻¹, which was 495% higher than that of pure UPE, showing a synergistic effect between BNs and CNTs. The simulations with Agari''s semi-empirical simulation suggested that increasing the CNT content contributed to synergistically assist BNs to form a better continuous and effective hybrid filler thermal network, thereby reducing phonon scattering and thermal resistance between BNs. In addition, UPE composites doped with BNs and CNTs presented better heat dissipation capacity and higher thermal stability as compared to that of pure UPE.

The carbon nanotubes (CNTs) synergistically assist boron nitride microsheets (BNs) to form a more continuous and effective thermal conduction path.     

Ethylene glycol nanofluids dispersed with monolayer graphene oxide nanosheet for high-performance subzero cold thermal energy storage

Ethylene glycol (EG) nanofluids have been intensively explored as one of the most promising solid–liquid phase change materials for subzero cold thermal energy storage (CTES). However, the prepared nanofluids usually suffer from a large supercooling degree, a long freezing period, reduced storage capacity and poor dispersion stability. Herein, we overcome these issues by developing stable EG nanofluids that are uniformly dispersed with low concentrations of monolayer ethanol-wetted graphene oxide nanosheets. The homogeneously dispersed monolayer sheet not only improves the thermal conductivity of the nanofluids (12.1%) but also provides the heterogeneous nucleation sites to trigger the crystal formation, thereby shortening the freezing time and reducing the supercooling degree. Compared with the base fluid, the nanofluids have reduced the supercooling degree by 87.2%, shortened the freezing time by 78.2% and maintained 98.5% of the latent heat. Moreover, the EG nanofluids have retained their initial stable homogeneous dispersion after repeated freezing/melting for 50 cycles, which ensures consistent CTES behavior during long-period operations. The facile preparation process, low loading requirement and consistent superior thermophysical properties would make the EG nanofluids loaded with monolayer graphene oxide sheets promising coolants for high-performance phase change-based CTES.

Homogeneously dispersed monolayer graphene oxide sheet in ethylene glycol solution enable a high-performance cold thermal energy storage.     

A supramolecular approach towards strong and tough polymer nanocomposite fibers

Polymer nanocomposite fibers are important one-dimensional nanomaterials that hold promising potential in a broad range of technological applications. It is, however, challenging to organize advanced polymer nanocomposite fibers with sufficient mechanical properties and flexibility. Here, we demonstrate that strong, tough and flexible polymer nanocomposite fibers can be approached by electrospinning of a supramolecular ensemble of dissimilar and complementary components including flexible multiwalled carbon nanotubes (CNT), and stiff cellulose nanocrystals (CNC) in an aqueous poly(vinyl alcohol) (PVA) system. CNT and CNC are bridged by a water-soluble aggregation-induced-emission (AIE) molecule that forms π–π stacking with CNT via its conjugated chains, and electrostatic attraction with CNC through its positive charges leading to a soluble CNT–AIE–CNC ensemble, which further assembles with PVA through hydrogen bonds. A high level of ordering of the nanoscale building blocks combined with hydrogen bonding leads to a more efficient stress transfer path between the reinforcing unit and the polymer. The nanocomposite fiber mat is capable of selective detection of nitroaromatic explosives.

Strong, tough and flexible polymer nanocomposite fibers can be approached by electrospinning of supramolecular ensemble of CNT–AIE–CNC/PVA in an aqueous system, which could be used for sensing.     

Investigating the effects of adding hybrid nanoparticles,graphene and boron nitride nanosheets,to octadecane on its thermal properties

Octadecane is an alkane that is used to store thermal energy at ambient temperature as a phase change material. A molecular dynamics study was conducted to investigate the effects of adding graphene and a boron nitride nanosheet on the thermal and structural properties of octadecane paraffin. The PCFF force field for paraffin, AIREBO potential for graphene, Tersoff potential for the boron nitride nanosheet, and Lennard-Jones potential for the van der Waals interaction between the nanoparticles and n-alkanes were used. Equilibrium and nonequilibrium molecular dynamics simulations were used to study the nano-enhanced phase change material properties. Results showed that the nanocomposite had a lower density change, more heat capacity (except at 300 K), more thermal conductivity, and a lower diffusion coefficient in comparison with pure paraffin. Additionally, the nanocomposite had a higher melting point, higher phonon density of state and radial distribution function peaks.

Octadecane is an alkane that is used to store thermal energy at ambient temperature as a phase change material.     

Self-healing microcapsules encapsulated with carbon nanotubes for improved thermal and electrical properties

Microcapsules are widely used by researchers in self-healing composites. In this study, multi-walled carbon nanotubes (CNT) were incorporated into the core of the microcapsules, along with the self-healing agent. Dicyclopentadiene (DCPD) and urea-formaldehyde (UF) were chosen as the core and shell materials respectively, and DCPD–CNT–UF based dual core microcapsules were synthesized. Two types of microcapsules, namely, DCPD–UF and DCPD–CNT–UF were successfully synthesized by the in situ polymerization technique. The novelty of this work is the development of dual core microcapsules with DCPD–CNT–UF combination. Surface morphology characterization and elemental analysis of the microcapsules were carried out using a scanning electron microscope (SEM-EDX). TGA and DSC analysis show that DCPD–CNT–UF microcapsules have better thermal stability than DCPD–UF microcapsules. These novel DCPD–CNT–UF microcapsules were found to be compatible with epoxy base resin for making resin castings. The presence of CNT is found to improve the mechanical, thermal and electrical properties of the resin cast specimens without compromising on self-healing efficiency.

Carbon nanotubes incorporated microcapsules based self-heating composites.     

Synthesis of highly stable γ-Fe2O3 ferrofluid dispersed in liquid paraffin,motor oil and sunflower oil for heat transfer applications

This article aims at the synthesis of highly stable γ-Fe₂O₃ magnetic nanoparticles and their ferrofluids using different base liquids such as liquid paraffin, motor oil and sunflower oil for heat transfer applications. Phase and morphology of the synthesized nanoparticles were probed using XRD, SEM and FTIR spectroscopy. The average nanoparticle size of γ-Fe₂O₃ magnetic nanoparticles was found to be 13 nm. Stability of the ferrofluids was monitored by visually observing the aggregation nature of the nanoparticles for 180 days. The ferrofluid prepared using motor oil as a base fluid exhibited high stability (for more than 1 year) and a mean enhancement of 77% in thermal conductivity at 1.5 vol% nanoparticles was observed as compared to base fluid. The viscosity of the ferrofluids was also measured and found to be 18, 38 and 8 cP at 27 °C for the liquid paraffin based, motor oil based and sunflower oil based ferrofluid, respectively.

Highly stable ferrofluid for greater enhancement of thermal conductivity.     

Characteristic analysis of three-ecofriendly reduced graphene oxides (rGOs) and their application in water–ethanol-based fluids with different volume ratios

In this paper, three-ecofriendly reduced graphene oxides (rGOs) were obtained by using three green reducing agents (beer, wine and cocoa) to reduce the graphene oxide (GO), and were labeled as B-rGO, W-rGO and C-rGO. Meanwhile, rGO nanofluids with different water–ethanol volume ratios (25 : 75, 50 : 50, 75 : 25) were prepared based on three-ecofriendly rGOs. The structure properties of the three-ecofriendly rGOs were investigated by XRD, FR-IT, Raman spectroscopy and XPS analysis. Meanwhile, the thermophysical properties of rGO nanofluids were analyzed. Experimental results indicated that the stability and thermophysical properties of rGO nanofluids were slightly different, indicating that the properties of the nanofluids are dependent on the type of base fluids and nanoparticles. When the water–ethanol volume ratio was maintained at 25 : 75, the stability experiment results showed that W-rGO nanofluids presented excellent stability, which indirectly confirmed their excellent thermal conductivity. Furthermore, the contact angle experiment indicated that the contact angles of rGO nanofluids decreased with the increase of temperature. In a word, these three rGOs and their nanofluids exhibited preferable properties that make them promising in the field of heat transfer.

Three ecofriendly reduced graphene oxides (rGOs) and rGO nanofluids with different water–ethanol volume ratios were prepared. The microstructure of rGO and the stability, thermal conductivity and contact angle of rGO nanofluids were investigated.     

CNT–TiO2 core–shell structure: synthesis and photoelectrochemical characterization

Porous composite coatings, made of a carbon nanotube (CNT)–TiO₂ core–shell structure, were synthesized by the hybrid CVD-ALD process. The resulting TiO₂ shell features an anatase crystalline structure that covers uniformly the surface of the CNTs. These composite coatings were investigated as photoanodes for the photo-electrochemical (PEC) water splitting reaction. The CNT–TiO₂ core–shell configuration outperforms the bare TiO₂ films obtained using the same process regardless of the deposited anatase thickness. The improvement factor, exceeding 400% in photocurrent featuring a core–shell structure, was attributed to the enhancement of the interface area with the electrolyte and the electrons fast withdrawal. The estimation of the photo-electrochemically effective surface area reveals that the strong absorption properties of CNT severely limit the light penetration depth in the CNT–TiO₂ system.

CNT–TiO₂ core–shell nanostructured coatings were made using a hybrid CVD/ALD process. The evaluation of these films as photoanodes for the photoelectrochemical water splitting reaction reveals a clear benefit from the involvement of CNTs.     

Preparation of PVDF/FMBO composite electrospun nanofiber for effective arsenate removal from water

In this study, novel electrospun nanofibers (NFs) composed of organic polyvinylidine fluoride (PVDF) and inorganic Fe–Mn binary oxide (FMBO) nanoparticles were fabricated using an electrospinning technique for adsorptive decontamination of As(v) from polluted water. The NFs were prepared with doped solutions consisting of different weight ratios of PVDF/FMBO, in a NF matrix, ranging from 0 to 0.5. SEM, XRD, FTIR and TEM then characterized the NFs and FMBO particles. The XRD analysis indicated successful impregnation of FMBO nanoparticles in the NF matrix of the NFs investigated. An As(v) adsorption capacity as high as around 21.32 mg g⁻¹ was obtained using the NF containing the highest amount of FMBO nanoparticles (designated as PVDF/FMBO 0.5). Furthermore, the adsorptive performance of the PVDF/FMBO 0.5 nanofiber could be easily regenerated using diluted alkaline solution (NaOH and NaOCl).

In this study, novel electrospun nanofibers composed of organic polyvinylidine fluoride and inorganic Fe–Mn binary oxide nanoparticles were fabricated using an electrospinning technique for adsorptive removal of As(v) from polluted water.     

Enhancement of thermal and mechanical properties of silicone rubber with γ-ray irradiation-induced polysilane-modified graphene oxide/carbon nanotube hybrid fillers

In this study, a polysilane-modified graphene oxide (GO) and carbon nanotube (CNT) nanocomposite (GO/CNTs-Si) was prepared as a thermal conductive nanofiller to enhance the thermal and mechanical properties of silicone rubber composites. By γ-ray-radiation 3-methacryloxypropyltrimethoxy silane (MPTMS) was polymerized on the surface of GO and CNTs to improve the interfacial interaction between the GO/CNTs-Si and SR matrix. FTIR characterization results demonstrated that polysilane modified the GO/CNTs successfully. The pristine GO/CNTs and resultant GO/CNTs-Si were individually incorporated into α,ω-dihydroxypolydimethylsiloxane to vulcanize SR composites. Compared with SR–GO/CNTs, SR–GO/CNT-Si exhibited better mechanical and thermal performance. Moreover, the time-dependent complex modulus of SR–GO/CNTs-Si was much higher than that of SR–GO/CNTs, which indicates longer service time and more stable performance. In terms of electronic packaging, SR–GO/CNTs exhibited better performance than the 1180B counterpart. The low value of warpage of chip packaged by SR–GO/CNTs implied that SR–GO/CNTs-Si could have potential application as the thermal interface electronic packaging material.

In this work, functionalized silicon rubber with hybrid nanocarbon filler was prepared. The composites with good resistance ability to stress relaxation can be used as underfill to improve the thermo-mechanical reliability of flip-chips.     

Self-dispersible graphene quantum dots in ethylene glycol for direct absorption-based medium-temperature solar-thermal harvesting

Poor dispersion stability of carbon nanofluids is one of the key issues limiting their solar-thermal applications especially under medium-to-high temperatures. Herein, this work reported a facile way to prepare stably dispersed graphene quantum dot-ethylene glycol (GQD-EG) medium-temperature solar-thermal nanofluids. The hydroxyl-terminated GQDs were synthesized by a scalable hydrothermal approach. The obtained GQDs have a small particle size, narrow particle size distribution and are self-dispersible within EG fluids. The GQD-EG nanofluids maintained their uniform dispersion after continuous heating at 180 °C for 7 days. The hydrogen bonding between the hydroxyl group on the surface of GQDs and the EG molecules helped achieve homogenous dispersion of GQDs in the nanofluids, and the small particle size and low density of GQDs helped mitigate the sedimentation tendency. The dispersed GQD-EG nanofluids have demonstrated broadband absorption of sunlight, high specific heat capacity and low viscosity, which are all desired for high-performance direct absorption-based solar-thermal energy. The prepared GQD-EG nanofluids have exhibited consistent volumetric harvesting of solar-thermal energy under concentrated solar illumination with a heating temperature up to 170 °C.

Self-dispersible graphene quantum dots in ethylene glycol enable stable nanofluidic solar-thermal energy harvesting at medium temperatures.     

Enhanced thermal conductivity of nanocomposites with MOF-derived encapsulated magnetic oriented carbon nanotube-grafted graphene polyhedra

It remains a challenge to develop highly polymer-based nanocomposite thermal interface materials, which can effectively remove heat developed during the miniaturization of electronic instruments. It has been reported that a large number of graphene-based nanocomposites exhibit excellent performance. However, it is still an issue to construct thermal conductive pathways by orientation arrangements with a low filler volume fraction. Herein, a high-thermal conductivity filler of magnetic carbon nanotube-grafted graphene polyhedra (Co@Co₃O₄-G) was exploited via the annealing of metal–organic frameworks (ZIF-67). Co@Co₃O₄-G can improve the thermal conductivity of nanocomposites obviously by forming oriented pathways for phonon transport in an external magnetic field. Therefore, the resulting nanocomposite displayed a high thermal conductivity of 2.11 W m⁻¹ K⁻¹ for only 8.7 vol%, which is 10 times higher than that of the pure epoxy resin. Core-shell magnetic cobalt oxide (Co@Co₃O₄) was encapsulated in situ in the nanoarchitecture to avoid falling off. Moreover, the equilibrium molecular dynamics (EMD) simulation verifies that Co@Co₃O₄-G had high thermal conductivity to effectively improve the heat dissipation of nanocomposites. This strategy provides an approach for developing high-performance thermal management materials and opens up the possibility for the pioneering applications of encapsulated magnetic-oriented thermal conductive fillers.

A high-thermal conductivity filler of magnetic carbon nanotube-grafted graphene polyhedra is exploited via annealing of a metal–organic framework (ZIF-67).     

Rapid preparation of ZnO nanocomposite hydrogels by frontal polymerization of a ternary DES and performance study

A deep eutectic solvent (DES) was synthesized from urea (U), acrylamide (AM), and choline chloride (ChCl). ZnO was dispersed in the DES as a filler, and nanocomposite hydrogels (ZnO/P(U-AM-ChCl)) were successfully prepared by frontal polymerization (FP). The hydrogels were verified by Fourier infrared spectroscopy to contain ZnO nanoparticles (ZnO-NPs). The swelling behaviour, conductivity, and antibacterial properties of the ZnO nanocomposite hydrogels were investigated. The results showed that the ZnO/P(U-AM-ChCl) hydrogels had excellent antibacterial properties and exhibited super high inhibition rates of 81.87% and 88.42% against two basic colonies of Gram-negative and Gram-positive bacteria, respectively. The equilibrium swelling of the hydrogels was found to increase significantly from 9.30 to 12.29 with the addition of ZnO, while the ZnO/P(U-AM-ChCl) hydrogel conductivity exhibited good UV sensitivity. This study provides a rapid and low-energy method for the preparation of nanocomposite hydrogels with excellent antibacterial properties.

This study provides a rapid and low-energy method for the preparation of nanocomposite hydrogels with excellent antibacterial properties.     

Synthesis of surfactant free stable nanofluids based on barium hexaferrite by pulsed laser ablation in liquid

Barium hexaferrite nanofluids based on five different solvents have been prepared by employing Pulsed Laser Ablation in Liquid (PLAL) at two different wavelengths of 532 nm and 1064 nm. They were then characterized using Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), X-ray Photoelectron Spectroscopy (XPS), UV-Vis spectroscopy, and Vibrating Sample Magnetometry (VSM). The chemical states of the ablated nanoparticles were identified from XPS analysis and found to be matching with that of the target. The crystallinity of the nanoparticles were confirmed from high resolution TEM (HRTEM) images and SAED patterns. It is found that different liquid environments lead to the formation of barium ferrite nanoparticles with different particle diameters. The plausible mechanism involved in this process is discussed. This study can pave way for the synthesis of stable magnetic nanofluids of permanent magnets. Further, this technique could be utilized for tailoring the morphology of nanoparticles with a judicious choice of the solvents and other ablation parameters.

Barium hexaferrite nanofluids based on five different solvents are prepared using pulsed laser ablation in liquid, the different solvents resulting in different particle diameters. This study paves the way for the synthesis of stable magnetic nanofluids of permanent magnets.     

Tailoring the reducibility and catalytic activity of CuO nanoparticles for low temperature CO oxidation

Copper oxide (CuO) nanoparticles have received considerable interest as active and inexpensive catalysts for various gas–solid reactions. The CuO reducibility and surface reactivity are of crucial importance for the high catalytic activity. Herein, we demonstrate that the reducibility and stability of CuO nanoparticles can be controlled and tailored for the high catalytic activity of CO oxidation. The synthesized CuO nanoparticles possessed enhanced reducibility in CO atmosphere at lower reduction temperature of 126 °C compared to 284 °C for that of reference CuO particles. Moreover, the CuO catalysts with tailored reducibility demonstrated a reaction rate of 35 μmol s⁻¹ g⁻¹ and an apparent activation energy of 75 kJ mol⁻¹. Furthermore, the tailored catalysts exhibited excellent long-term stability for CO oxidation for up to 48 h on stream. These readily-reducible CuO nanoparticles could serve as efficient, inexpensive and durable catalysts for CO oxidation at low temperatures.

Copper oxide (CuO) nanoparticles of tailored reducibility could be used as inexpensive, efficient and durable catalysts for CO oxidation at low temperature.     

Polyhedral oligosilsesquioxane-modified boron nitride enhances the mechanical properties of polyimide nanocomposites

A novel high-strength polyimide (PI) nanocomposite film was designed and constructed by the copolymerization of epoxidized polyhedral oligomeric silsesquioxane-modified hexagonal boron nitride and polyamic acid (PAA). The composite filler (EPPOSS@Gh-BN) was composed of silane coupling agent KH550 modified hexagonal boron nitride (Gh-BN) and epoxidized polyhedral oligomeric silsesquioxanes (EPPOSS), which improved not only the dispersion of the h-BN but also the effective interfacial stress transfer, leading to an enhanced mechanical strength of the resultant PI nanocomposite film of 114 MPa even with a slight EPPOSS@Gh-BN loading of 0.30 wt%, and the storage modulus was increased by more than 30% to 4 GPa compared to pure PI. Meanwhile, the PI/EPPOSS@Gh-BN nanocomposite has better heat transfer performance, higher hydrophobicity, lower dielectric properties, and higher heat stability than pure PI, and is therefore expected to provide an ideal platform for the development of highly flexible electronics in the future.

A novel high-strength polyimide nanocomposite film was obtained by the copolymerization of epoxidized polyhedral oligomeric silsesquioxane-modified hexagonal boron nitride and polyamic acid.     

The influence of covalent and non-covalent functionalization of GNP based nanofluids on its thermophysical,rheological and suspension stability properties

Covalent functionalization (CF-GNPs) and non-covalent functionalization (NCF-GNPs) approaches were applied to prepare graphene nanoplatelets (GNPs). The impact of using four surfactants (SDS, CTAB, Tween-80, and Triton X-100) was studied with four test times (15, 30, 60, and 90 min) and four weight concentrations. The stable thermal conductivity and viscosity were measured as a function of temperature. Fourier transform infrared spectroscopy (FTIR), thermo-gravimetric analysis (TGA), X-ray diffraction (XRD) and Raman spectroscopy verified the fundamental efficient and stable CF. Several techniques, such as dispersion of particle size, FESEM, FETEM, EDX, zeta potential, and UV-vis spectrophotometry, were employed to characterize both the dispersion stability and morphology of functionalized materials. At ultrasonic test time, the highest stability of nanofluids was achieved at 60 min. As a result, the thermal conductivity displayed by CF-GNPs was higher than NCF-GNPs and distilled water. In conclusion, the improvement in thermal conductivity and stability displayed by CF-GNPs was higher than those of NCF-GNPs, while the lowest viscosity was 8% higher than distilled water, and the best thermal conductivity improvement was recorded at 29.2%.

Covalent functionalization (CF-GNPs) and non-covalent functionalization (NCF-GNPs) approaches were applied to prepare graphene nanoplatelets (GNPs).