Search

In the original publication [...]

Nanoparticle additives increase the thermal conductivity of conventional heat transfer fluids at low concentrations, which leads to improved heat transfer fluids and processes. This study investigates lignin-coated magnetic nanocomposites (lignin@Fe3O4) as a novel bio-based magnetic nanoparticle additive to enhance the thermal conductivity of aqueous-based fluids. Kraft lignin was used to encapsulate the Fe3O4 nanoparticles to prevent agglomeration and oxidation of the magnetic nanoparticles. Lignin@Fe3O4 nanoparticles were prepared using a pH-driven co-precipitation method with a 3:1 lignin to magnetite ratio and characterized by X-ray diffraction, FT-IR, thermogravimetric analysis, and transmission electron microscopy. The magnetic properties were characterized using a vibrating sample magnetometer. Once fully characterized, lignin@Fe3O4 nanoparticles were dispersed in aqueous 0.1% w/v agar–water solutions at five different concentrations, from 0.001% w/v to 0.005% w/v. Thermal conductivity measurements were performed using the transient line heat source method at various temperatures. A maximum enhancement of 10% in thermal conductivity was achieved after adding 0.005% w/v lignin@Fe3O4 to the agar-based aqueous suspension at 45 °C. At room temperature (25 °C), the thermal conductivity of lignin@Fe3O4 and uncoated Fe3O4 agar-based suspensions was characterized at varying magnetic fields from 0 to 0.04 T, which were generated using a permanent magnet. For this analysis, the thermal conductivity of lignin magnetic nanosuspensions initially increased, showing a 5% maximum peak increase after applying a 0.02 T magnetic field, followed by a decreasing thermal conductivity at higher magnetic fields up to 0.04 T. This result is attributed to induced magnetic nanoparticle aggregation under external applied magnetic fields. Overall, this work demonstrates that lignin-coated Fe3O4 nanosuspension at low concentrations slightly increases the thermal conductivity of agar aqueous-based solutions, using a simple permanent magnet at room temperature or by adjusting temperature without any externally applied magnetic field.

Abstract A novel route to fabricating hybrid ceramic matrix composites has been developed. The fabrication is based on the unique combination of additive manufacturing (AM), a preceramic polymer, and a chopped carbon fiber precursor. After introducing the photoinitiator to the preceramic polymer formulation, a photosensitive resin was introduced. The resulting resin was loaded with distinct weight percentages of stabilized polyacrylonitrile nanofiber—the carbon fiber precursor. These formulations were 3D printed, cured, and converted to ceramic phases using a pyrolysis cycle. The end objective of the pyrolysis cycle is the conversion of the polycarbosilane resin into a silicon carbide matrix and the transformation of the PAN polymer into reinforcing carbon nanofibers within one cycle. The results of this work showed that ceramic matrix composite components can be successfully fabricated using a suitable combination of 3D printing, resin formulation, and processing cycle. The pyrolyzed ceramic hybrid composite was fully dense with nearly linear shrinkage and a shiny, smooth surface. Approximately 60% retained weight after pyrolysis to 1350°C was confirmed by thermogravimetric analysis. In terms of crystallography, the ceramic matrix composite displayed three coexisting phases including silicon carbide, silicon oxycarbide, and turbostratic carbon. The results showed this combination of material and processes has a high potential for fabricating hybrid composites with high‐temperature performance and improved mechanical properties combined with complex geometries.

Smart and mechanically flexible energy harvesting/storage devices are attractive for the immensely growing electronic, automobile, medical, and aerospace markets. The leading challenges with current devices are their limitations regarding installation on curvy design, high-manufacturing cost, and lower production rate. Therefore, new design strategies in terms of new materials, cost, and ability to scale up fabrication are imperative to meet the contemporary and future demands of these fast-growing markets. Flexographic printing is one of the newest technologies that promises cost-effective energy devices with better energy harvesting and high storage performance. Current knowledge, selection of suitable materials, and methods of flexographic printing for solar cell and battery construction are reviewed and summarized in this paper in comparison to existing printing technologies. The main purpose of this review is to provide a comprehensive idea of flexographic printing for energy devices.

Lignin macromolecules are potential precursor materials for producing electrospun nanofibers for composite applications. However, little is known about the effect of lignin type and blend ratios with synthetic polymers. This study analyzed blends of poly(acrylonitrile-co-methyl acrylate) (PAN-MA) with two types of commercially available lignin, low sulfonate (LSL) and alkali, kraft lignin (AL), in DMF solvent. The electrospinning and polymer blend solution conditions were optimized to produce thermally stable, smooth lignin-based nanofibers with total polymer content of up to 20 wt % in solution and a 50/50 blend weight ratio. Microscopy studies revealed that AL blends possess good solubility, miscibility, and dispersibility compared to LSL blends. Despite the lignin content or type, rheological studies demonstrated that PAN-MA concentration in solution dictated the blend’s viscosity. Smooth electrospun nanofibers were fabricated using AL depending upon the total polymer content and blend ratio. AL’s addition to PAN-MA did not affect the glass transition or degradation temperatures of the nanofibers compared to neat PAN-MA. We confirmed the presence of each lignin type within PAN-MA nanofibers through infrared spectroscopy. PAN-MA/AL nanofibers possessed similar morphological and thermal properties as PAN-MA; thus, these lignin-based nanofibers can replace PAN in future applications, including production of carbon fibers and supercapacitors.