Carbon Nanofibers Grown In Situ on Porous Glass

2017 ◽  
Vol 50 ◽  
pp. 1-17
Author(s):  
M. Alejandra Mazo ◽  
Javier Sanguino ◽  
Aitana Tamayo ◽  
Juan Rubio

Carbon nanofibers (CNFs) were grown in situ on porous glass at different temperatures and times using a Ni acetate catalyst and CH4/N2 as a carbon source. The porous glass was obtained by acid leaching of phase separated borosilicate glass, which generates a broad size distribution of mesopores (≈20 nm). Subsequent impregnation with Ni acetate reduces the pore size to ≈ 4 nm but also creates new micropores, thus increasing the surface area. During thermal treatment the surface area decreases as temperature rises, mainly due to shrinkage of the glassy matrix; however new pores are created at ≈ 70 nm (mainly at 600 oC) associated to the generation of CNFs on the glass surface, indicating this temperature offers the best conditions. The CNFs grow inside and fill in the micro-mesopores in the porous glass. They do not grow at 500 oC as the Ni acetate is not transformed into metallic Ni. Ni deactivation occurs at temperatures over 700 oC, thus reducing the formation of CNFs. At 1000 oC the degradation of CH4 leads to a thickening of the CNFs. The thermal degradation of the CNFs occurs in two steps, the first (360-416oC) corresponding to CNFs grown on the glass surface and the second (518-649oC) to CNFs grown inside the glass pores. Treatment times over 2 h lead to the deactivation of Ni, pore shrinkage and hence lower CNF yields.

RSC Advances ◽  
2019 ◽  
Vol 9 (57) ◽  
pp. 33539-33548
Author(s):  
Hua Liu ◽  
Weiguo Song ◽  
Aihua Xing

K2S was found to be an excellent in situ activation agent for the fabrication of electrospun carbon nanofibers with large surface area (835.0 m2 g−1) and hierarchical meso/microporous structures.


Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 82 ◽  
Author(s):  
Sayaka Yanagida ◽  
Kentaro Hirayama ◽  
Kenichiro Iwasaki ◽  
Atsuo Yasumori

Combinations of TiO2 photocatalysts and various adsorbents have been extensively investigated for eliminating volatile organic compounds (VOCs) at low concentrations. Herein, TiO2 and porous glass cloth composites were prepared by acid leaching and subsequent TiO2 dip-coating of the electrically applied glass (E-glass) cloth, and its adsorption and photocatalytic ability were investigated. Acid leaching increased the specific surface area of the E-glass cloth from 1 to 430 m2/g while maintaining sufficient mechanical strength for supporting TiO2. Further, the specific surface area remained large (290 m2/g) after TiO2 coating. In the photocatalytic decomposition of gaseous 2-propanol, the TiO2-coated porous glass cloth exhibited higher adsorption and photocatalytic decomposition ability than those exhibited by the TiO2-coated, non-porous glass cloth. The porous composite limited desorption of acetone, which is a decomposition intermediate of 2-propanol, until 2-propanol was completely decomposed to CO2. The CO2 generation rate was affected by the temperature condition (15 or 35 °C) and the water content (2 or 18 mg/L); the latter also influenced 2-propanol adsorption in photocatalytic decomposition. Both the conditions may change the diffusion and adsorption behavior of 2-propanol in the porous composite. As demonstrated by its high adsorption and photocatalytic ability, the composite (TiO2 and porous glass cloth) effectively eliminates VOCs, while decreasing the emission of harmful intermediates.


1996 ◽  
Vol 465 ◽  
Author(s):  
J. Wei ◽  
P. Van Iseghem

ABSTRACTDuring the reaction of HLW glass with interstitial clay water at different temperatures with various ratios of glass surface area to solution volume (SA/V) and durations, Eu released from the glass forms predominantly Eu-humate colloids (organic colloids) by a complexation reaction. The size distribution and stability of Eu-humate colloids have been characterized. It is likely that inorganic colloids which are mainly composed of Si, Al and Ca are generated from the corrosion of waste glass by a nucleation reaction.


RSC Advances ◽  
2014 ◽  
Vol 4 (88) ◽  
pp. 47414-47420 ◽  
Author(s):  
Zi Ping Wu ◽  
Man Zhao ◽  
Jing Wei Hu ◽  
Wei Bo Zhang ◽  
Yan Hong Yin ◽  
...  

H2WO4 sheets approximately 50 nm long and 20 nm wide were prepared using a DWCNT template, and WC nanosheets with large surface areas were obtained when the H2WO4 was carbonized at a low temperature using a liquid carbon source.


2019 ◽  
Vol 33 (14n15) ◽  
pp. 1940016 ◽  
Author(s):  
Rounak R. Atram ◽  
Bhawana A. Manekar ◽  
Subhash B. Kondawar ◽  
Ramdas G. Atram ◽  
Pankaj Koinkar

Novel unique fabrication of ZnO nanoparticles decorated graphene beaded carbon nanofibers (G-CNF) encapsulated by polyaniline (PANI) nanocomposites through three steps by electrospinning, hydrothermal and in-situ polymerization is reported. As-synthesized G-CNF/ZnO/PANI and CNF/ZnO/PANI nanocomposites were comparatively studied by scanning electron microscopy and electrochemical characterizations for supercapacitor application. Electrochemical measurements of G-CNF/ZnO/PANI electrode revealed the maximum specific capacitance, discharge time, energy density and power density as compared to that of CNF/ZnO/PANI indicating the increase in surface area due to graphene incorporation in electrospinning of carbon nanofibers. The combination of electric double layer charge (EDLC) capacitance from high surface area of G-CNF and pseudo-capacitance from PANI and ZnO nanoparticles facilitates the synergistic effect of ternary components to enhance the electrochemical performance of G-CNF/ZnO/PANI nanocomposite.


Author(s):  
K. Fukushima ◽  
N. Kohyama ◽  
A. Fukami

A film-sealed high resolution environmental cell(E.C) for observing hydrated materials had been developed by us(l). Main specification of the E.C. is as follows: 1) Accelerated voltage; 100 kV. 2) Gas in the E.C.; saturated water vapour with carrier gas of 50 Torr. 3) Thickness of gas layer; 50 μm. 4) Sealing film; evaporated carbon film(20 nm thick) with plastic microgrid. 5) Resolving power; 1 nm. 6) Transmittance of electron beam; 60% at 100 kV. The E.C. had been successfully applied to the study of hydrated halloysite(2) (3). Kaolin minerals have no interlayer water and are basically non-expandable but form intercalation compounds with some specific chemicals such as hydrazine, formamide and etc. Because of these compounds being mostly changed in vacuum, we tried to reveal the structure changes between in wet air and in vacuum of kaolin minerals intercalated with hydrazine and of hydrated state of montmori1lonite using the E.C. developed by us.


Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1885
Author(s):  
Xinyu Wu ◽  
Feng Yang ◽  
Jian Gan ◽  
Zhangqian Kong ◽  
Yan Wu

The silver particles were grown in situ on the surface of wood by the silver mirror method and modified with stearic acid to acquire a surface with superhydrophobic and antibacterial properties. Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and X-ray energy spectroscopy (XPS) were used to analyze the reaction mechanism of the modification process. Scanning electron microscopy (SEM) and contact angle tests were used to characterize the wettability and surface morphology. A coating with a micro rough structure was successfully constructed by the modification of stearic acid, which imparted superhydrophobicity and antibacterial activity to poplar wood. The stability tests were performed to discuss the stability of its hydrophobic performance. The results showed that it has good mechanical properties, acid and alkali resistance, and UV stability. The durability tests demonstrated that the coating has the function of water resistance and fouling resistance and can maintain the stability of its hydrophobic properties under different temperatures of heat treatment.


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