To produce a three-dimensional micro/nanocarbon structure, a manufacturing design technique for sub-10 nm carbon fiber arrays on three-dimensional carbon micropillars has been developed; the method involves initiating electrostatic jetting, forming submicron-to-nanoscale PAN-based fibers, and maximizing the shrinkage from polyacrylonitrile (PAN)-based fibers to carbon fibers. Nanoforming and nanodepositing methods for polyacrylonitrile-based jet fibers as precursors of carbon fibers are proposed for the processing design of electrostatic jet initiation and for the forming design of submicron-to-nanoscale PAN-based fibers by establishing and analyzing mathematical models that include the diameter and tensile stress values of jet fibers and the electric field intensity values on the surfaces of carbon micropillars. In accordance with these methods, an array of jet fibers with diameters of ~80 nm is experimentally formed based on the thinning of the electrospinning fluid on top of a dispensing needle, the poking of drum into an electrospinning droplet, and the controlling of the needle-drum distance. When converting thin PAN-based jet fibers to carbon fibers, a pyrolysis method consisting of the suspension of jet nanofibers between carbon micropillars, the bond between the fibers and the surface of the carbon micropillar, and the control of micropillar spacing, stabilization temperature, and carbonation rate is presented to maximize the shrinkage from PAN-based fibers to carbon fibers and to form sub-10 nm carbon fiber arrays between three-dimensional carbon micropillars. The manufacturing design of a three-dimensional micro/nanocarbon structure can produce thin PAN-based jet nanofibers and nanofiber arrays aligned on micropillar surfaces, obtain shrinkage levels reaching 96% and incorporate sub-10 nm carbon fibers into three-dimensional carbon micropillars; these actions provide new research opportunities for correlated three-dimensional micro/nanocarbon structures that have not previously been technically possible.
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http://dx.doi.org/10.1038/s41378-023-00604-1 | DOI Listing |
Acc Mater Res
December 2024
The Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia 30332, United States.
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View Article and Find Full Text PDFUltrason Sonochem
December 2024
Department of Family and Consumer Sciences, North Carolina A&T State University, Greensboro, NC 27411, USA. Electronic address:
Sweet potatoes are a rich source of nutrients and bioactive compounds, but their quality can be impacted by the drying process. This study investigates the impact of slot jet reattachment (SJR) nozzle and ultrasound (US) combined drying (SJR + US) on sweet potato quality, compared to freeze-drying (FD), SJR drying, and hot air drying (HAD). SJR + US drying at 50 °C closely resembled FD in enhancing quality attributes and outperformed HAD and SJR in key areas such as rehydration, shrinkage ratios, and nutritional composition.
View Article and Find Full Text PDFSensors (Basel)
December 2024
Sensor Systems Group, School of Electrical & Electronic Engineering, The University of Sheffield, Portobello Centre, Pitt Street, Sheffield S1 4ET, UK.
This study introduces a novel approach to analysing the combustion process using a high-speed, non-contact, optical fibre-coupled Si avalanche photodiode (APD)-based infrared radiation thermometer (IRT). The Si APD-IRT, combined with an optimised field-programmable gate array (FPGA)-based digital design, achieves a response time of 1 µs, faster than commercially available instruments. Our instrument captures the entire ignition and reignition cycle of a Jet A kerosene droplet with high temporal precision within a combustion chamber, a feat impossible with traditional thermocouples.
View Article and Find Full Text PDFPolymers (Basel)
December 2024
School of Chemical Engineering, Pusan National University, Busan 46241, Republic of Korea.
In this study, a transient viscosity adjustment method using a coaxial nozzle was explored to fabricate nanofibers from non-spinnable -poly(hydroxyamide) (-PHA). Unlike conventional electrospinning methods that often require additives to induce fiber formation, this approach relies on a sheath-core configuration, introducing tetrahydrofuran (THF) to the sheath to temporarily adjust solution viscosity. The diffusion of THF into the core -PHA solution resulted in momentary solidification at the interface, promoting nanofiber formation without compromising polymer solubility.
View Article and Find Full Text PDFSmall
November 2024
Department of Materials, University of Oxford, Parks Road, Oxford, OX1 3PH, UK.
Nanofibrous active layers offer hierarchical control over molecular structure, and the size and distribution of electron donor:acceptor domains, beyond conventional organic photovoltaic architectures. This structure is created by forming donor pathways via electrospinning nanofibers of semiconducting polymer, then infiltrating with an electron acceptor. Electrospinning induces chain and crystallite alignment, resulting in enhanced light-harvesting and charge transport.
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