Browse
Submit Data
Databases
API
Help

Dataset Information

26 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Experimental data showing the influence of different boron nitride particles on the silica network, the butyl stearate and the porogens in shape-stabilized phase change materials.

ABSTRACT: Shape-stabilized phase change materials (ss-PCMs) based on silica and butyl stearate were thermally enhanced via the addition of different hexagonal boron nitride particles (BN) to the in situ sol-gel synthesis. The dataset is used in conjunction with the experimental data of the influence of the particle size and surface area of BN on the thermal and mechanical properties of ss-PCMs discussed in Marske et al. (2021). To study the effect of the different BN particles on the hydrolysis degree of the silica network and on the chemical nature of the porogens sodium dodecyl sulfate and poly(vinyl alcohol) used for the ss-PCM synthesis, the ss-PCM samples are measured via High Power Decoupling (HPDEC) Magic Angle Spinning (MAS) ²⁹Si NMR and attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy, respectively. Additionally, data of the influence of BN on the thermal properties is presented as thermogravimetric analysis (TG). The ²⁹Si MAS NMR spectra are referenced to tetramethylsilane and show the different silica species in ppm. The different value of wavenumber and intensity of each reference and ss-PCM sample is listed in the IR spectra. The decomposition points of the ss-PCMs are calculated from the TG data via OriginLab. The spectra and data can be used as a reference for other researchers and engineers to use in synthesizing ss-PCMs based on silica and other polymeric materials or as reference for pure BN, SDS, stabilized silica sol and PVA.

SUBMITTER: Marske F

PROVIDER: S-EPMC8487010 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Fabrication of covalently linked exfoliated boron nitride nanosheet/multi-walled carbon nanotube hybrid particles for thermal conductive composite materials.

Project description:Boron nitride nanosheet (BNNS)/multi-walled carbon nanotube (MWCNT) hybrid particles were synthesized for use as a conductive filler for epoxy and polyphenylene sulfide (PPS). BNNSs were prepared via the exfoliation of bulk boron nitride (BN) particles. Micrometer-sized BN particles were exfoliated to form nanosheets, and their surfaces were modified using 3-aminopropyltriethoxysilane (APTES). The amine groups on the BNNS surface were reacted with acid-treated MWCNTs, and covalently connected BNNS/MWCNT particles were synthesized. Moreover, a chemical reaction without agitation increased the particle connection during the hybrid particle preparation, resulting in a large number of MWCNTs being introduced onto the BNNSs. The BNNS/MWCNT hybrid particle composite had better thermal conductivity than BNNSs or a BNNS/MWCNT composite without chemical bonding based on the same filler contents and composition. This was because of the particle connections establishing three-dimensional heat conducting path in a matrix, which affected the thermal conductivity of the composite.

| S-EPMC9086474 | biostudies-literature

Magneto-Adaptive Surfactants Showing Anti-Curie Behavior and Tunable Surface Tension as Porogens for Mesoporous Particles with 12-Fold Symmetry.

Project description:Gaining external control over self-organization is of vital importance for future smart materials. Surfactants are extremely valuable for the synthesis of diverse nanomaterials. Their self-assembly is dictated by microphase separation, the hydrophobic effect, and head-group repulsion. It is desirable to supplement surfactants with an added mode of long-range and directional interaction. Magnetic forces are ideal, as they are not shielded in water. We report on surfactants with heads containing tightly bound transition-metal centers. The magnetic moment of the head was varied systematically while keeping shape and charge constant. Changes in the magnetic moment of the head led to notable differences in surface tension, aggregate size, and contact angle, which could also be altered by an external magnetic field. The most astonishing result was that the use of magnetic surfactants as structure-directing agents enabled the formation of porous solids with 12-fold rotational symmetry.

| S-EPMC5485036 | biostudies-literature

New 2D Structural Materials: Carbon-Gallium Nitride (CC-GaN) and Boron-Gallium Nitride (BN-GaN) Heterostructures-Materials Design Through Density Functional Theory.

Project description:New class of ternary nanohetrostructures have been proposed by mixing 2D gallium nitride (GaN) with graphene and 2D hexagonal boron nitride (BN) with an aim towards desgining innovative 2D materials for applications in electronics and other industries. The structural stability and electronic properties of these nanoheterostructures have been analyzed using first-principles based calculations done in the framework of density functional theory. Different structure patterns have been analyzed to identify the most stable structures. It is found to be more energetically favorable that the carbon atoms occupy the positions of the nitrogen atoms in a clustered pattern in CC-GaN heterostructures, whereas boron doping is preferred in the reverse order, where isolated BN and GaN layered configurations are preferred in BN-GaN heterostructures. These 2D nanoheterostructures are energetically favored materials with direct band gap and have potential application in nanoscale semiconducting and nanoscale optoelectronic devices.

| S-EPMC6647944 | biostudies-literature

Chemisorption of Hydroxide on 2D Materials from DFT Calculations: Graphene versus Hexagonal Boron Nitride.

Project description:Recent nanofluidic experiments revealed strongly different surface charge measurements for boron-nitride (BN) and graphitic nanotubes when in contact with saline and alkaline water (Nature 2013, 494, 455-458; Phys. Rev. Lett. 2016, 116, 154501). These observations contrast with the similar reactivity of a graphene layer and its BN counterpart, using density functional theory (DFT) framework, for intact and dissociative adsorption of gaseous water molecules. Here we investigate, by DFT in implicit water, single and multiple adsorption of anionic hydroxide on single layers. A differential adsorption strength is found in vacuum for the first ionic adsorption on the two materials-chemisorbed on BN while physisorbed on graphene. The effect of implicit solvation reduces all adsorption values, resulting in a favorable (nonfavorable) adsorption on BN (graphene). We also calculate a pKa ≃ 6 for BN in water, in good agreement with experiments. Comparatively, the unfavorable results for graphene in water echo the weaker surface charge measurements but point to an alternative scenario.

| S-EPMC5360233 | biostudies-literature

Liquid crystals of neat boron nitride nanotubes and their assembly into ordered macroscopic materials.

Project description:Boron nitride nanotubes (BNNTs) have attracted attention for their predicted extraordinary properties; yet, challenges in synthesis and processing have stifled progress on macroscopic materials. Recent advances have led to the production of highly pure BNNTs. Here we report that neat BNNTs dissolve in chlorosulfonic acid (CSA) and form birefringent liquid crystal domains at concentrations above 170 ppmw. These tactoidal domains merge into millimeter-sized regions upon light sonication in capillaries. Cryogenic electron microscopy directly shows nematic alignment of BNNTs in solution. BNNT liquid crystals can be processed into aligned films and extruded into neat BNNT fibers. This study of nematic liquid crystals of BNNTs demonstrates their ability to form macroscopic materials to be used in high-performance applications.

| S-EPMC9174261 | biostudies-literature

Porous Boron Nitride Materials: Influence of Structure, Chemistry and Stability on the Adsorption of Organics.

Project description:Porous boron nitride (BN) is structurally analogous to activated carbon. This material is gaining increasing attention for its potential in a range of adsorption and chemical separation applications, with a number of recent proof-of-concept studies on the removal of organics from water. Today though, the properties of porous BN-i.e., surface area, pore network, chemistry-that dictate adsorption of specific organics remain vastly unknown. Yet, they will need to be optimized to realize the full potential of the material in the envisioned applications. Here, a selection of porous BN materials with varied pore structures and chemistries were studied for the adsorption of different organic molecules, either directly, through vapor sorption analyses or as part of a water/organic mixture in the liquid phase. These separations are relevant to the industrial and environmental sectors and are envisioned to take advantage of the hydrophobic character of the BN sheets. The materials were tested and regenerated and their physical and chemical features were characterized before and after testing. This study allowed identifying the adsorption mechanisms, assessing the performance of porous BN compared to benchmarks in the field and outlining ways to improve the adsorption performance further.

| S-EPMC6443638 | biostudies-literature

Enhanced Thermal Conductivity of Epoxy Composites Filled with Al2O3/Boron Nitride Hybrids for Underfill Encapsulation Materials.

Project description:In this study, a thermal conductivity of 0.22 W·m-1·K-1 was obtained for pristine epoxy (EP), and the impact of a hybrid filler composed of two-dimensional (2D) flake-like boron nitride (BN) and zero-dimensional (0D) spherical micro-sized aluminum oxide (Al2O3) on the thermal conductivity of epoxy resin was investigated. With 80 wt.% hybrid Al2O3-BN filler contents, the thermal conductivity of the EP composite reached 1.72 W·m-1·K-1, increasing approximately 7.8-fold with respect to the pure epoxy matrix. Furthermore, different important properties for the application were analyzed, such as Fourier-transform infrared (FTIR) spectra, viscosity, morphology, coefficient of thermal expansion (CTE), glass transition temperature (Tg), decomposition temperature (Td), dielectric properties, and thermal infrared images. The obtained thermal performance is suitable for specific electronic applications such as flip-chip underfill packaging.

| S-EPMC7795928 | biostudies-literature

Boron Nitride-Doped Polyphenylenic Organogels.

Project description:Herein, we describe the synthesis of the first boron nitride-doped polyphenylenic material obtained through a [4 + 2] cycloaddition reaction between a triethynyl borazine unit and a biscyclopentadienone derivative, which undergoes organogel formation in chlorinated solvents (the critical jellification concentration is 4% w/w in CHCl3). The polymer has been characterized extensively by Fourier-transform infrared spectroscopy, solid-state 13C NMR, solid-state 11B NMR, and by comparison with the isolated monomeric unit. Furthermore, the polymer gels formed in chlorinated solvents have been thoroughly characterized and studied, showing rheological properties comparable to those of polyacrylamide gels with a low crosslinker percentage. Given the thermal and chemical stability, the material was studied as a potential support for solid-state electrolytes. showing properties comparable to those of polyethylene glycol-based electrolytes, thus presenting great potential for the application of this new class of material in lithium-ion batteries.

| S-EPMC9753561 | biostudies-literature

Polymorphism of bulk boron nitride.

Project description:Boron nitride (BN) is a material with outstanding technological promise due to its exceptional thermochemical stability, structural, electronic, and thermal conductivity properties, and extreme hardness. Yet, the relative thermodynamic stability of its most common polymorphs (diamond-like cubic and graphite-like hexagonal) has not been resolved satisfactorily because of the crucial role played by kinetic factors in the formation of BN phases at high temperatures and pressures (experiments) and by competing bonding and electrostatic and many-body dispersion forces in BN cohesion (theory). This lack of understanding hampers the development of potential technological applications and challenges the boundaries of fundamental science. Here, we use high-level first-principles theories that correctly reproduce all important electronic interactions (the adiabatic-connection fluctuation-dissipation theorem in the random phase approximation) to estimate with unprecedented accuracy the energy differences between BN polymorphs and thus overcome the accuracy hurdle that hindered previous theoretical studies. We show that the ground-state phase of BN is cubic and that the frequently observed hexagonal polymorph becomes entropically stabilized over the cubic at temperatures slightly above ambient conditions (T c→h = 335 ± 30 K). We also reveal a low-symmetry monoclinic phase that is extremely competitive with the other low-energy polymorphs and that could explain the origins of the experimentally observed "compressed h-BN" phase. Our theoretical findings therefore should stimulate new experimental efforts in bulk BN and promote the use of high-level theories in modeling of technologically relevant van der Waals materials.

| S-EPMC6357755 | biostudies-literature

Toxicity evaluation of boron nitride nanospheres and water-soluble boron nitride in <i>Caenorhabditis elegans</i>.

Project description:Boron nitride (BN) nanomaterials have been increasingly explored for potential biological applications. However, their toxicity remains poorly understood. Using Caenorhabditis elegans as a whole-animal model for toxicity analysis of two representative types of BN nanomaterials - BN nanospheres (BNNSs) and highly water-soluble BN nanomaterial (named BN-800-2) - we found that BNNSs overall toxicity was less than soluble BN-800-2 with irregular shapes. The concentration thresholds for BNNSs and BN-800-2 were 100 µg·mL-1 and 10 µg·mL-1, respectively. Above this concentration, both delayed growth, decreased life span, reduced progeny, retarded locomotion behavior, and changed the expression of phenotype-related genes to various extents. BNNSs and BN-800-2 increased oxidative stress levels in C. elegans by promoting reactive oxygen species production. Our results further showed that oxidative stress response and MAPK signaling-related genes, such as GAS1, SOD2, SOD3, MEK1, and PMK1, might be key factors for reactive oxygen species production and toxic responses to BNNSs and BN-800-2 exposure. Together, our results suggest that when concentrations are lower than 10 µg·mL-1, BNNSs are more biocompatible than BN-800-2 and are potentially biocompatible material.

| S-EPMC5571844 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data