Farm-waste-derived recyclable photothermal evaporator

© The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Tian, Y., Liu, X., Li, J., Deng, Y., DeGiorgis, J. A., Zhou, S., Caratenuto, A., Minus, M. L., Wan, Y., Xiao, G., & Zheng, Y. Farm-waste-derived recyclable photothermal evaporator. Cell Reports Physical Science, 2(9), (2021): 100549, https://doi.org/10.1016./j.xcrp.2021.100549Interfacial solar steam generation is emerging as a promising technique for efficient desalination. Although increasing efforts have been made, challenges exist for achieving a balance among a plethora of performance indicators—for example, rapid evaporation, durability, low-cost deployment, and salt rejection. Here, we demonstrate that carbonized manure can convert 98% of sunlight into heat, and the strong capillarity of porous carbon fibers networks pumps sufficient water to evaporation interfaces. Salt diffusion within microchannels enables quick salt drainage to the bulk seawater to prevent salt accumulation. With these advantages, this biomass-derived evaporator is demonstrated to feature a high evaporation rate of 2.81 kg m−2 h−1 under 1 sun with broad robustness to acidity and alkalinity. These advantages, together with facial deployment, offer an approach for converting farm waste to energy with high efficiency and easy implementation, which is particularly well suited for developing regions.This project is supported by the National Science Foundation through grant no. CBET-1941743. This project is based upon work supported in part by the National Science Foundation under EPSCoR Cooperative Agreement no. OIA-1655221

Solid-State Spun Fibers from 1 mm Long Carbon Nanotube Forests Synthesized by Water-Assisted Chemical Vapor Deposition

In this work, we report continuous carbon nanotube fibers dry-drawn directly from water-assisted CVD grown forests with millimeter scale length. As-drawn nanotube fibers exist as aerogel and can be transformed into more compact fibers through twisting or densification with a volatile liquid. Nanotube fibers are characterized by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Raman microscopy and wide-angle X-ray diffraction (WAXD). Mechanical behavior and electrical conductivity of the post-treated nanotube fibers are investigated

Blending for Achieving Theoretical Mechanical and Electrical Property Enhancement in Polyacrylonitrile/SWNT Materials

Filtration based processing of nanotube and polymer-nanotube dispersions is used to create polymer and nano-filler hybrid materials. The composite morphology consists of two layers: (1) a region where polymer chains have direct matrix interaction with the nano-fillers and (2) a nano-filler rich region excluded from matrix interactions. The experimental work here demonstrates the processing of this hybrid material using polyacrylonitrile (PAN) and single-wall carbon nanotubes (SWNT) at various PAN/SWNT weight concentrations. Mechanical analyses were performed to evaluate effective contributions from the SWNT in each of the defined layers. The region of high matrix-filler interactions exhibits blending behavior with material properties following suit. As a result, mechanical performance is consistent and begins to exceed theoretical predictions derived from Halpin–Tsai calculations. Tensile strength and modulus reached values as high as 60 MPa and 7.7 GPa, respectively, surpassing the performance of neat nano-filler (36 MPa, 3.9 GPa) and neat polymer matrix (44 MPa, 2.0 GPa) films. Additionally, the measurement of electrical properties shows that the blended polymer-SWNT region exhibits conductivity comparable to the filler. The results of this work suggest that blending polymers and nano-fillers is possible and may facilitate the production of materials with comparatively high mechanical performance and electrical conductivities

Single wall carbon nanotube templated oriented crystallization of poly(vinyl alcohol)

Shearing of poly(vinyl alcohol) (PVA)/single wall carbon nanotube (SWNT) dispersions result in the formation of self-assembled oriented PVA/SWNT fibers or ribbons, while PVA solution results in the formation of unoriented fibers. Diameter/width and length of these self-assembled fibers was 5-45 ??m and 0.5-3 mm, respectively. High-resolution transmission electron micrographs showed well resolved PVA (200) lattice with molecules oriented parallel to the nanotube axis. Nanotube orientation in the self-assembled fibers was also determined from Raman spectroscopy. PVA fibers exhibited about 48% crystallinity, while crystallinity in PVA/SWNT fibers was 84% as determined by wide angle X-ray diffraction. PVA and carbon nanotubes were at an angle of 25-40?? to the self-assembled fiber axis. In comparison to PVA, PVA/SWNT samples exhibited significantly enhanced electron beam radiation resistance. This study shows that single wall carbon nanotubes not only nucleate polymer crystallization, but also act as a template for polymer orientation. ??? 2006 Elsevier Ltd. All rights reserved.close10711

Oriented and exfoliated single wall carbon nanotubes in polyacrylonitrile

Polyacrylonitrile (PAN)/single wall carbon nanotubes (SWNT) fibers were gel spun at 0, 0.5, and 1 wt% SWNT content to a draw ratio of 51. Structure, morphology, and mechanical and dynamic mechanical properties of these fibers have been studied. PAN/SWNT composite exhibited much higher electron beam radiation resistance than PAN. As a result, PAN lattice images could be easily observed in the composite fiber by high resolution transmission electron microscopy. The PAN/SWNT composite fiber also exhibited higher solvent resistance than the control PAN fiber. UV-vis spectroscopy of highly drawn fiber exhibited van Hove transitions, suggesting SWNT exfoliation upon drawing. SWNT exfoliation was also confirmed by high resolution transmission electron microscopy (HRTEM). At 1 wt% SWNT loading, fiber storage modulus (at 1 Hz) increased by 13.9, 6.6, and 0.2 GPa at -75, 25, and 150 ??C, respectively. This suggests that the load transfer ability and hence interfacial strength is increasing with decreasing temperature, even below the polymer's ?? transition temperature. ??? 2006 Elsevier Ltd. All rights reserved.close9310

Blending for Achieving Theoretical Mechanical and Electrical Property Enhancement in Polyacrylonitrile/SWNT Materials

Filtration based processing of nanotube and polymer-nanotube dispersions is used to create polymer and nano-filler hybrid materials. The composite morphology consists of two layers: (1) a region where polymer chains have direct matrix interaction with the nano-fillers and (2) a nano-filler rich region excluded from matrix interactions. The experimental work here demonstrates the processing of this hybrid material using polyacrylonitrile (PAN) and single-wall carbon nanotubes (SWNT) at various PAN/SWNT weight concentrations. Mechanical analyses were performed to evaluate effective contributions from the SWNT in each of the defined layers. The region of high matrix-filler interactions exhibits blending behavior with material properties following suit. As a result, mechanical performance is consistent and begins to exceed theoretical predictions derived from Halpin–Tsai calculations. Tensile strength and modulus reached values as high as 60 MPa and 7.7 GPa, respectively, surpassing the performance of neat nano-filler (36 MPa, 3.9 GPa) and neat polymer matrix (44 MPa, 2.0 GPa) films. Additionally, the measurement of electrical properties shows that the blended polymer-SWNT region exhibits conductivity comparable to the filler. The results of this work suggest that blending polymers and nano-fillers is possible and may facilitate the production of materials with comparatively high mechanical performance and electrical conductivities

Carbon nanotube reinforced small diameter polyacrylonitrile based carbon fiber

Polyacrylonitrile (PAN) and PAN/carbon nanotube (CNT) composite (99/1) based carbon fibers with an effective diameter of about 1 ??m have been processed using island-in-a-sea bi-component cross-sectional geometry and gel spinning. PAN/CNT (99/1) based carbon fibers processed using this approach exhibited a tensile strength of 4.5 GPa (2.5 N/tex) and tensile modulus of 463 GPa (257 N/tex), while these values for the control PAN-based carbon fiber processed under the similar conditions were 3.2 GPa (1.8 N/tex) and 337 GPa (187 N/tex), respectively. Properties of these 1 ??m diameter carbon fibers have been compared to the properties of the larger diameter (>6 ??m) PAN and PAN/CNT based carbon fibers. ??? 2008 Elsevier Ltd.close566

Carbon nanotube dispersion and exfoliation in polypropylene and structure and properties of the resulting composites

Nitric acid treated single and multi wall carbon nanotubes (SWNT and MWNT) have been dispersed in polypropylene using maleic anhydride grafted polypropylene (MA-g-PP) and butanol/xylene solvent mixture. SWNT exfoliation was characterized by Raman and UV-vis-NIR spectroscopies. Evidence for hydrogen bonding between maleic anhydride grafted polypropylene and nitric acid treated nanotubes was obtained using infrared spectroscopy. Polypropylene/carbon nanotube composites were melt-spun into fibers. Dynamic mechanical studies show that for fibers containing 0.1 wt% SWNT, storage modulus increased by 5 GPa at -140 ??C and by about 1 GPa at 100 ??C, suggesting temperature dependent interfacial strength. The crystallization behavior has been monitored using differential scanning calorimetry and optical microscopy. Control fibers exhibited 27% shrinkage at 160 ??C, while the shrinkage in the composite fibers was less than 5%. Fibers heat-treated to 170 ??C show very narrow polypropylene melting peak (peak width about 1 ??C). ??? 2008 Elsevier Ltd. All rights reserved.close778

Structural Polymer-Based Carbon Nanotube Composite Fibers: Understanding the Processing–Structure–Performance Relationship

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