Search Results (38)

Hexagonal boron nitride (h-BN) and boron nitride nanotubes (BNNTs) are emerging advanced nanomaterials with analogous structures to graphene and carbon nanotubes, respectively. However, little is known about what effect replacing carbon atoms with boron and nitrogen will have on the materials’ safety profile. This study’s aim was to first identify if multi-walled nanotubes of BN could produce a hazard profile similar to that evidenced already for multi-walled carbon nanotubes (MWCNTs) and secondly if the material when present in a sheet-like structure increases or decreases the hazard profile. Fish are aquatic organisms sensitive to boron compounds; however, the potential hazard following exposure to BN and especially when present in such nanostructures has not yet been investigated. An in vitro testing platform consisting of multiple cell lines of the rainbow trout, Oncorhynchus mykiss (RTH-149, RTG-2, RTL-W1 and RTgill-W1), was used in a first-hazard screening approach for cytotoxicity and to gain information on material–cellular interaction. Clear differences were evidenced in material uptake, leading to plasma membrane disruption accompanied with a loss in metabolic activity for BNNTs at lower exposure concentrations compared to h-BN. As in the case of carbon nanotubes, close attention must be given to potential interferences with assays based on optical readouts. Full article

Boron nitride nanotubes (BNNTs) are predicted to be promising one-dimensional nonlinear optical materials, but to date, only one experimental observation has been made using individual nanotubes. In this work, second harmonic generation (SHG) was achieved from free-standing bulk BNNT sheets and BNNT coatings on silica substrates. Focusing femtosecond infrared (fs-IR) laser pulses with a wavelength of 800 nm onto the BNNT assemblies resulted in strong SHG at a wavelength of 400 nm. It was observed that due to the thickness variation of the BNNT assemblies and orientational alignment of BNNTs in the assemblies, the intensity of the second-harmonic (SH) radiation changed dramatically when different locations on the samples were investigated. Among all the BNNT assemblies tested, the localized SH response and its dependence on the polarization of the excitation fs-IR pulses were the strongest in BNNT coatings produced by a dip-coating process. By measuring the SH response, the uniformity, reproducibility, and efficiency of BNNT deposition processes could be assessed. For applications requiring a high SH response from BNNT assemblies, the process of dip coating is preferred. Full article

Since epoxy resin has excellent mechanical and insulating qualities, it is frequently utilized in dry transformers. Low thermal conductivity, however, has prevented it from be developed further in high-frequency and large-capacity dry transformers. This study describes the preparation of sheet boron nitride (BN)/epoxy resin composites with superior electrical, thermal, and mechanical properties through the application of varying strengths of high-frequency alternating-current (AC) electric fields. Using an optical microscope, the orienting process of BN in epoxy resin under an electric field was studied. In parallel, tests were conducted on the BN/epoxy resin composites made with varying electric field strengths. The findings indicate that the preparation using a high-frequency AC electric field decreases BN agglomeration and improves the composite’s properties. The overall performance is comparatively ideal when the applied electric field strength is 30 V/mm, the tensile strength is 48.3 MPa, the breakdown field strength is 37.65 kV/mm, and the thermal conductivity of the BN/epoxy resin composite is 0.95 W/(m·K). The thermal conductivity greatly increased and BN was organized into chains when the electric field approached 60 V/mm. The tensile strength and breakdown field strength, on the other hand, declined. Full article

Recent findings have demonstrated that the desalination and purification of contaminated water and the separation of ions and gases, besides solutions to other related issues, may all be achieved with the use of membranes based on artificial nanoporous materials. Before the expensive stages of production and experimental testing, the optimum size and form of membrane nanopores could be determined using computer-aided modeling. The notion that rectangular nanopores created in a multilayered hexagonal boron nitride (h-BN) membrane in a way that results in different inner lining atoms would exhibit unique properties in terms of the water penetration rate is put forth and examined in the current study. Nanopores in boron nitride sheets can be generated with the inner lining of boron atoms (B-edged), nitrogen atoms (N-edged), or both boron and nitrogen atoms (BN-edged). In this study, we compared the three different inner-lined nanopores of boron nitride nanosheets to a comparable-sized graphene nanopore and evaluated the water conduction. Full article

Two-dimensional (2D) hexagonal boron carbon nitride (h-B_xC_yN_z) has garnered a lot of interest in the last two decades because of its remarkable physical and chemical characteristics. Because of the carbon atoms, it has a smaller gap than its cousin, boron nitride, and is hence more appropriate for a wider range of applications. In the frame of density functional theory, we discuss the structural, electronic, and magnetic properties of mono Ti-doped and Co-doped BC₆N (Ti/Co-BC₆N) at different sites of substitutional doping (Ti/Co) in the BC₆N monolayer. The mono substitutional doping at the B (Ti_B/Co_B), N (Ti_N/Co_N), and two different C (C1 (Ti_C1/Co_C1), C2 (Ti_C2/Co_C2)) sites, are investigated. The position of the Ti/Co dopant is an important parameter that changes the electronic state, magnetic moment, and adsorption activity of the pristine BC₆N nanosheet. We find that the adsorption of the gases NO, NO₂, CO₂, NH₃, N₂, and O₂ is significantly improved on the doped sheet at all doped positions compared to the adsorption on the pristine structure. The Ti/Co-BC₆N can adsorb NO and NO₂ better than CO₂ and NH₃. Ti_C1-BC₆N and Ti_B-BC₆N are the best doped sheets for adsorbing NO and NO₂, respectively. The CO₂ and the N₂ molecules are moderately adsorbed at all doped positions as compared to the other adsorbed molecules. Ti-doped sheets can adsorb the CO₂, NH₃, and O₂ better than the corresponding Co-doped sheets. We also study the adsorption of molecular hydrogen on our single-atom Ti/Co-doped systems, as well as on 4-atom Ti and Co clusters embedded in the BC₆N sheets. We show that the cluster-embedded sheets can adsorb up to four H₂ molecules. These novel findings are important for many applications of BC₆N, including spintronics, gas filtration, molecular sensing, and hydrogen storage. Full article

The stacking of two-dimensional atomic-level thickness materials onto hexagonal boron nitride (h-BN) and graphene (Gr) not only significantly enhances their properties, but also exhibits a multitude of exceptional characteristics, promising widespread applications across various fields. Clay minerals hold profound significance in scientific research not only because of their abundance but also because of their application in geology, environmental science, materials science, and biotechnology. We present a study that uses density functional theory (DFT) to analyze the effect on the mechanical properties of lizardite slab-reinforced Gr or h-BN monolayers. In addition to the reference lizardite slab (Liza-2D), six composites were studied: a monolayer of Gr (h-BN) over the octahedral face of a pristine lizardite slab (Liza-Gr1 (Liza-BN1)), a monolayer of Gr (h-BN) under the tetrahedral face of a pristine lizardite slab (Liza-Gr2(Liza-BN2)), and a pristine lizardite slab sandwiched between two Gr (h-BN) monolayers (Liza-Gr3(Liza-BN3)). We observed that reinforcement by Gr or h-BN significantly increased the bulk, Young’s and shear moduli of the composites. Taking into account that the Gr and h-BN sheets interact weakly by van der Waals interactions with the lizardite slab surface, we estimated the Young’s and shear moduli of the composites by the Rule of Mixtures and obtained a reasonable agreement with those from DFT calculations. Full article

Using the first-principles calculation, two doping two-dimensional (2D) BN (boron nitride) polymorphs are constructed in this work. The two doping 2D BN polymorphs B₅N₆Al and B₅N₆C sheets are thermally stable under 500 K. All the B₆N₆, B₅N₆Al, and B₅N₆C sheets are semiconductor materials with indirect band gaps on the basis of a hybrid functional. The anisotropic calculation results indicate that Young’s modulus (E) and Poisson’s ratio (v) of the B₆N₆, B₅N₆Al, and B₅N₆C sheets are anisotropic in the xy plane. In addition, the magnetic properties of the B₆N₆, B₅N₆Al, and B₅N₆C sheets have also been investigated. According to the calculation of the magnetic properties, B₆N₆ sheet does not exhibit magnetism, while it shows weak magnetism after doping carbon atom to the BN sheet. This paper explores the influence mechanism of doping different atoms on the basic physical properties of two-dimensional BN sheets. It not only constructs a relationship between structure and performance but also provides theoretical support for the performance regulation of BN materials. Full article

Emergent heat transfer and thermal management applications require polymer composites with enhanced thermal conductivity (κ). Composites filled with non-spherical fillers, such as hexagonal boron nitride (hBN) and Graphite (Gr), suffer from processing-induced filler orientations, resulting in anisotropic κ, commonly low in the through-plane direction. Here, the effects of extrusion and compression molding-induced orientations on κ of hBN- and Gr-filled polyethylene composites were investigated. The effect of extrusion on the hBN orientation was studied using dies of various shapes. The shaped extrudates exhibited hBN orientations parallel to the extrusion flow direction, which prompted additional hBN orientation during compression molding. κ of the composites produced with shaped extrudates varied from 0.95 to 1.67 W m⁻¹ K⁻¹. Pelletizing and crushing the extrudates improved κ, by exploiting and eliminating the effect of extrusion-induced hBN orientations. Gr-filled composites showed better κ than hBN composites due to the higher intrinsic conductivity and bigger particle sizes. A maximum κ of 5.1 and 11.8 W m⁻¹ K⁻¹ was achieved in composites with oriented hBN and Gr through a thin rectangular die and stacking the sheets to fabricate composites with highly oriented fillers. Full article

With the rapid development of the electronics industry, there is a growing demand for packaging materials that possess both high thermal conductivity (TC) and low electrical conductivity (EC). However, traditional insulating fillers such as boron nitride, aluminum nitride, and alumina (Al₂O₃) have relatively low intrinsic TC. When graphene, which exhibits both superhigh TC and EC, is used as a filler to fill epoxy resin, the TC of blends can be much higher than that of blends containing more traditional fillers. However, the high EC of graphene limits its application in cases where electrical insulation is required. To address this challenge, a method for coating graphene sheets with an in situ grown Al₂O₃ layer has been proposed for the fabrication of epoxy-based composites with both high TC and low EC. In the presence of a cationic surfactant, a dense Al₂O₃ layer with a network structure can be formed on the surface of graphene sheets. When the total content of Al₂O₃ and graphene mixed filler reached 30 wt%, the TC of the epoxy composite reached 0.97 W m⁻¹ K⁻¹, while the EC remained above 10¹¹ Ω·cm. Finite element simulations accurately predicted TC and EC values in accordance with experimental results. This material, with its combination of high TC and good insulation properties, exhibits excellent potential for microelectronic packaging applications. Full article

This study investigates the effect of adding stearic acid (SA) on the thermal conductivity of polyamide 6 (PA6)/boron nitride (BN) composites. The composites were prepared by melt blending, and the mass ratio of PA6 to BN was fixed at 50:50. The results show that when the SA content is less than 5 phr, some SA is distributed at the interface between BN sheets and PA6, which improves the interface adhesion of the two phases. This improves the force transfer from the matrix to BN sheets, promoting the exfoliation and dispersion of BN sheets. However, when the SA content was greater than 5 phr, SA tends to aggregate and form separate domains rather than being dispersed at the interface between PA6 and BN. Additionally, the well-dispersed BN sheets act as a heterogeneous nucleation agent, significantly improving the crystallinity of the PA6 matrix. The combination of good interface adhesion, excellent orientation, and high crystallinity of the matrix leads to efficient phonon propagation, resulting in a significant improvement in the thermal conductivity of the composite. The highest thermal conductivity of the composite is achieved when the SA content is 5 phr, which is 3.59 W m⁻¹ K⁻¹. The utilization of a composite material consisting of 5phr SA as the thermal interface material displays the highest thermal conductivity, and the composite also demonstrates satisfactory mechanical properties. This study proposes a promising strategy for the preparation of composites with high thermal conductivity. Full article

With the improvement of the conversion efficiency of LED chip and fluorescent material and the increasing demand for high-brightness light sources, LED technology has begun to move toward the direction of high-power. However, there is a huge problem that high-power LED must face with a large amount of heat generated by high power causing a high temperature thermal decay or even thermal quenching of the fluorescent material in the device, resulting in a reduction of the luminous efficiency, color coordinates, color rendering index, light uniformity, and service life of LED. In order to solve this problem, fluorescent materials with high thermal stability and better heat dissipation were prepared to enhance their performance in high-power LED environments. A variety of boron nitride nanomaterials were prepared by the solid phase-gas phase method. By adjusting the ratio of boric acid to urea in the raw material, different BN nanoparticles and nanosheets were obtained. Moreover, the control of catalyst amount and synthesis temperature can be used to synthesize boron nitride nanotubes with various morphologies. By adding different morphologies and quantities of BN material in PiG (phosphor in glass), the mechanical strength, heat dissipation, and luminescent properties of the sheet can be effectively controlled. PiG prepared by adding the right number of nanotubes and nanosheets has higher quantum efficiency and better heat dissipation after being excited by high power LED. Full article

With increasing heat accumulation in advanced modern electronic devices, dielectric materials with high thermal conductivity (λ) and excellent electrical insulation have attracted extensive attention in recent years. Inspired by mussel, hexagonal boron nitride (hBN) and graphene oxide (GO) are assembled to construct mhBN@GO hybrids with the assistance of poly(catechol-polyamine). Then, mhBN@GO hybrids are dispersed in carboxy nitrile rubber (XNBR) latex via emulsion coprecipitation to form elastomer composites with a high λ and satisfactory insulating properties. Thanks to the uniform dispersion of mhBN@GO hybrids, the continuous heat conduction pathways exert a significant effect on enhancing the λ and decreasing the interface thermal resistance of XNBR composites. In particular, the λ value of 30 vol% mhBN@GO/XNBR composite reaches 0.4348 W/(m·K), which is 2.7 times that of the neat XNBR (0.1623 W/(m·K)). Meanwhile, the insulating hBN platelets hinder the electron transfer between adjacent GO sheets, leading to satisfactory electrical insulation in XNBR composites, whose AC conductivity is as low as 10⁻¹⁰ S/cm below 100 Hz. This strategy opens up new prospects in the assembly of ceramic and carbonaceous fillers to prepare dielectric elastomer composites with high λ and satisfactory electrical insulation, making them promising for modern electrical systems. Full article

Thermal transport simulations were performed to investigate the important factors affecting the thermal conductivity based on the structure of semi-crystalline polyetheretherketone (PEEK), and the addition of boron nitride (BN) sheets. The molecular-level structural analysis facilitated the prediction of the thermal conductivity of the optimal structure of PEEK reflecting the best parameter value of the length of amorphous chains, and the ratio of linkage conformations, such as loops, tails, and bridges. It was found that the long heat transfer paths of polymer chains were induced by the addition of BN sheets, which led to the improvement of the thermal conductivities of the PEEK/BN composites. In addition, the convergence of the thermal conductivities of the PEEK/BN composites in relation to BN sheet size was verified by the disconnection of the heat transfer path due to aggregation of the BN sheets. Full article

Despite the availability of nano and submicron-sized additive materials, the controlled incorporation and utilization of these additives remain challenging due to their difficult handling ability and agglomeration-prone properties. The formation of composite granules exhibiting unique microstructure with desired additives distribution and good handling ability has been reported using the electrostatic integrated granulation method. This study demonstrates the feasible controlled incorporation of two-dimensional hexagonal boron nitride (hBN) sheets with alumina (Al₂O₃) particles, forming Al₂O₃–hBN core–shell composite granules. The sintered artifacts obtained using Al₂O₃–hBN core–shell composite granules exhibited an approximately 28% higher thermal conductivity than those obtained using homogeneously hBN-incorporated Al₂O₃ composite granules. The findings from this study would be beneficial for developing microstructurally controlled composite granules with the potential for scalable fabrication via powder-metallurgy inspired methods. Full article

Aramid, chemically known as para phenylene terephthalamide or PPD-T, has been widely used in the reinforcement of telecommunication cables, rubber materials (transmission belts, pneumatic belts), ballistic clothing, and frictional materials primarily due to their high tensile resistance, high elastic modulus, and excellent thermal stability (−80–200 °C). These unique properties of aramid originate from its chemical structure, which consists of relatively rigid polymer chains linked by benzene rings and amide bonds (-CO-NH-). Here, in this work inspired by these properties, a heat spreader called Thermal Interface Material (TIM) is developed by synthesizing a resin from scrap aramid fibers. When hexagonal boron nitride (h-BN) as filler is introduced into the as-synthesized aramid resin to form a thin film of thermal sheet (50 μm), an in-plane thermal conductivity as high as 32.973 W/mK is achieved due to the firmly stacked and symmetric arrangement of the h-BN in the resin matrix. Moreover, the influence of h-BN platelet size is studied by fabricating thermal sheets with three different sizes of h-BN (6–7.5 μm, 15–21 μm, and 30–35 μm) in the aramid resin. The results of the study show that as platelet size increases, thermal conductivity increases significantly. Since the resin reported herein is developed out of scrap aramid fibers, the cost involved in the manufacture of the thermal sheet will be greatly lower. As the thermal sheet is designed with h-BN rather than graphene or carbonaceous materials, this high heat spreading sheet can be employed for 5G antenna modules where properties like a low dielectric constant and high electrical insulation are mandated. Full article