Electrospun flexible lignin/polyacrylonitrile-based carbon nanofiber and its application in electrode materials for supercapacitors

2021 ◽  
pp. 004051752110371
Author(s):  
Hong Wu ◽  
Chengkun Liu ◽  
Zhiwei Jiang ◽  
Zhi Yang ◽  
Xue Mao ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Electrode Materials ◽  
Carbon Nanofiber ◽  
Electrochemical Impedance ◽  
Nickel Foam ◽  
Average Diameter ◽  
Raw Material ◽  
Equivalent Series Resistance

In this study, a lignin/polyacrylonitrile (PAN) composite nanofiber membrane is prepared by electrospinning and used as the precursor to prepare flexible carbon nanofibers (CNFs) through pre-oxidation and carbonization. The micromorphology, crystal structure, pore size distribution and specific surface area of the CNFs are characterized by field emission scanning electron microscopy, X-ray diffraction, Raman spectroscopy and specific surface adsorption analysis, respectively. The electrochemical properties of the CNF membrane are also investigated by cyclic voltammetry, galvanostatic charge–discharge and electrochemical impedance spectroscopy due to its potential application in binder-free electrode materials for supercapacitors. We successfully prepared flexible CNFs with an average diameter of about 539 nm and a specific surface area of 1053.78 m2/g when the mass ratio of lignin to PAN was 9:1 in a solution concentration of 28 wt%. The CNFs are loaded onto nickel foam to prepare the electrode materials for supercapacitors without a binder. When the current density is 0.5 A/g, the specific capacitance could be up to 201.27 F/g and the equivalent series resistance is only 0.57 Ω, which shows an excellent electrochemical performance. This study not only provides a theoretical basis for the high-value utilization of lignin and the preparation of flexible lignin/PAN-based CNFs, but also provides a new type of environmentally friendly raw material for the electrodes of supercapacitors and could be helpful to alleviate the energy crisis and environmental pollution.

scholarly journals Hydrothermal Synthesis of Co-Doped NiSe2 Nanowire for High-Performance Asymmetric Supercapacitors

Materials ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 1468 ◽  
Author(s):  
Yun Gu ◽  
Le-Qing Fan ◽  
Jian-Ling Huang ◽  
Cheng-Long Geng ◽  
Jian-Ming Lin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Energy Density ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Electrode Materials ◽  
Nickel Foam ◽  
High Energy ◽  
High Energy Density ◽  
Asymmetric Supercapacitor

Co@NiSe2 electrode materials were synthesized via a simple hydrothermal method by using nickel foam in situ as the backbone and subsequently characterized by scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and a specific surface area analyzer. Results show that the Co@NiSe2 electrode exhibits a nanowire structure and grows uniformly on the nickel foam base. These features make the electrode show a relatively high specific surface area and electrical conductivity, and thus exhibit excellent electrochemical performance. The obtained electrode has a high specific capacitance of 3167.6 F·g−1 at a current density of 1 A·g−1. To enlarge the potential window and increase the energy density, an asymmetric supercapacitor was assembled by using a Co@NiSe2 electrode and activated carbon acting as positive and negative electrodes, respectively. The prepared asymmetrical supercapacitor functions stably under the potential window of 0–1.6 V. The asymmetric supercapacitor can deliver a high energy density of 50.0 Wh·kg−1 at a power density of 779.0 W·kg−1. Moreover, the prepared asymmetric supercapacitor exhibits a good rate performance and cycle stability.

scholarly journals New Electrodes Prepared from Mineral and Plant Raw Materials of Kazakhstan

2016 ◽  
Vol 18 (2) ◽  
pp. 141 ◽  
Author(s):  
A.A. Atchabarova ◽  
R.R. Tokpayev ◽  
A.T. Kabulov ◽  
S.V. Nechipurenko ◽  
R.A. Nurmanova ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Electrode Materials ◽  
Raw Materials ◽  
Hydrothermal Carbonization ◽  
Walnut Shell ◽  
High Background ◽  
Plant Raw Materials ◽  
Developed Surface

<p>Electrode materials were prepared from activated carbonizates of walnut shell, apricot pits and shungite rock from “Bakyrchik” deposit, East Kazakhstan. Physicochemical characteristics of the obtained samples were studied by the Brunauer-Emett-Taylor method, scanning electron microscopy, Raman spectroscopy and other methods. Electrochemical properties of the obtained materials were studied by the method of cyclic voltammetry. It was found that the samples have an amorphous structure. Samples based on plant raw materials after hydrothermal carbonization at 240 °С during 24 h, have more homogeneous and developed surface. Specific surface area of carbon containing materials based on apricot pits is 1300 m<sup>2</sup>/g, for those on the based on mineral raw material, it is 153 m<sup>2</sup>/g. It was shown that materials after hydrothermal carbonization can be used for catalytic purposes and electrodes after thermal carbonization for analytical and electrocatalytic purposes. Electrode obtained by HTC have electrocatalytic activity. CSC 240 has high background current (slope i/Е is 43 mА V<sup>–1</sup> cm<sup>–2</sup>), low potential of the hydrogen electroreduction (more positive by ~ 0.5 V than samples based on plant raw materials). The reaction of DA determination is more pronounced on the electrodes obtained by HTC 240 °C, 24 h, due to the nature, carbon structure and high specific surface area of obtained samples.</p>

scholarly journals Preparation of Zirconia Nanofibers by Electrospinning and Calcination with Zirconium Acetylacetonate as Precursor

Polymers ◽  
2019 ◽  
Vol 11 (6) ◽  
pp. 1067 ◽  
Author(s):  
Vyacheslav V. Rodaev ◽  
Svetlana S. Razlivalova ◽  
Andrey O. Zhigachev ◽  
Vladimir M. Vasyukov ◽  
Yuri I. Golovin
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Heterogeneous Catalysts ◽  
Tetragonal Zirconia ◽  
Nitrogen Adsorption ◽  
Average Diameter ◽  
High Specific Surface Area ◽  
X Ray ◽  
Adsorption Analysis

For the first time, zirconia nanofibers with an average diameter of about 75 nm have been fabricated by calcination of electrospun zirconium acetylacetonate/polyacrylonitrile fibers in the range of 500–1100 °C. Composite and ceramic filaments have been characterized by scanning electron microscopy, thermogravimetric analysis, nitrogen adsorption analysis, energy-dispersive X-ray spectroscopy, and X-ray diffractometry. The stages of the transition of zirconium acetylacetonate to zirconia have been revealed. It has been found out that a rise in calcination temperature from 500 to 1100 °C induces transformation of mesoporous tetragonal zirconia nanofibers with a high specific surface area (102.3 m2/g) to non-porous monoclinic zirconia nanofibers of almost the same diameter with a low value of specific surface area (8.3 m2/g). The tetragonal zirconia nanofibers with high specific surface area prepared at 500 °C can be considered, for instance, as promising supports for heterogeneous catalysts, enhancing their activity.

Study on Nano-Hydroxyapatite Assisted Preparing by Ionic Liquids

2014 ◽  
Vol 1015 ◽  
pp. 501-504 ◽  
Author(s):  
Yong Guang Bi ◽  
Xu Si Xu
Keyword(s):  
Grain Size ◽  
Ionic Liquids ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Large Scale ◽  
Preparation Method ◽  
Raw Material ◽  
Large Scale Preparation ◽  
Scale Preparation

Papers with Ca (NO3)2• 4H2O and (NH4)2HPO4as raw material, prepared by ionic liquids assisted nanoHAP, resulting hexagonal nanoHAP are crystal grain size are 10-20nm level, are smaller nanometer range ; specific surface area, the findings show that ionic liquids have the technology to promote the significance of the preparation method can provide a reference for large-scale preparation of biomedical nanomaterials.

Synthesis and Thermal Stability of HfO2 Nanoparticles

2010 ◽  
Vol 1256 ◽  
Author(s):  
Girija Shankar Chaubey ◽  
Yuan Yao ◽  
Julien Pierre Amelie Makongo Mangan ◽  
Pranati Sahoo ◽  
Pierre F. P. Poudeu ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Large Scale ◽  
Average Diameter ◽  
Scale Production ◽  
Simple Method ◽  
Good Thermal Stability ◽  
Large Scale Production

AbstractA simple method is reported for the synthesis of monodispersed HfO2 nanoparticles by the ammonia catalyzed hydrolysis and condensation of hafnium (IV) tert-butoxide in the presence of surfactants at room temperature. Transmission electron microscopy shows faceted nanoparticles with an average diameter of 3-4 nm. As-synthesized nanoparticles are amorphous in nature and crystallize upon moderate heat treatment. The HfO2 nanoparticles have a narrow size distribution, large specific surface area and good thermal stability. Specific surface area was about 239 m2/g on as-prepared nanoparticle samples while those annealed at 500 °C have specific surface area of 221 m2/g indicating that there was no significant increase in particle size. This result was further confirmed by TEM images of nanoparticles annealed at 300 °C and 500 °C. X-ray diffraction studies of the crystallized nanoparticles revealed that HfO2 nanoparticles were monoclinic in structure. The synthetic procedure used in this work can be readily modified for large scale production of monodispersed HfO2 nanoparticles.

Preparation of Adsorbent from Blue Coke Powder and its Application in Coking Wastewater

2011 ◽  
Vol 695 ◽  
pp. 553-556
Author(s):  
Yu Hong Tian ◽  
Xin Zhe Lan ◽  
Qiu Li Zhang ◽  
Juan Qin Xue ◽  
Yong Hui Song ◽  
...  
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Removal Rate ◽  
Nitrogen Concentration ◽  
Ammonia Nitrogen ◽  
Raw Material ◽  
Coking Wastewater ◽  
Adsorption Time ◽  
Coke Powder

The low-cost blue coke industrial by-product, blue coke powder was used as raw material for the production of porous carbons adsorbent by steam activating at temperature of 800°C under the atmosphere of N2 for 60 minutes. The specific surface area and pore properties of the adsorbent were characterized by using N2 adsorption-desorption isotherms. Furthermore, the adsorption effects of the adsorbent for ammonia nitrogen in coking wastewater were investigated in terms of particle size, dosage of absorbent and adsorption time. The results show that the specific surface area is 620.94m2/g, the total pore volume is 0.4442cm3/g and the average mesopore size is 4.5808nm, the adsorbent possesses predominant mesoporous structures. In aeration, the removal rate of ammonia nitrogen can reach to 39.5% under the conditions of the ammonia nitrogen concentration of 625mg/L, the dosage of adsorbent 10g/L at the adsorption time of 60 minutes.

BCN nanosheets templated by g-C3N4 for high performance capacitive deionization

2018 ◽  
Vol 6 (30) ◽  
pp. 14644-14650 ◽  
Author(s):  
Shiyong Wang ◽  
Gang Wang ◽  
Tingting Wu ◽  
Yunqi Zhang ◽  
Fei Zhan ◽  
...  
Keyword(s):  
Specific Surface ◽  
Pore Structure ◽  
Surface Area ◽  
Specific Surface Area ◽  
High Performance ◽  
Electrode Materials ◽  
High Specific Surface Area ◽  
Capacitive Deionization ◽  
First Time

BCN nanosheets show a pore structure with a high specific surface area and are investigated as CDI electrode materials for the first time.

scholarly journals Properties of materials for advanced technology of joint utilization of man-made waste

2019 ◽  
Vol 58 (6) ◽  
pp. 97-103
Author(s):  
Igor N. Tanutrov ◽  
◽  
Marina N. Sviridova ◽  
Sergey A. Lyamkin ◽  
Yury A. Chesnokov ◽  
...  
Keyword(s):  
Particle Size ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Granulometric Composition ◽  
Average Diameter ◽  
Water Soluble ◽  
Advanced Technology ◽  
Particle Sizes ◽  
Main Components

With the aim of improving the technology of co-processing of red mud (RM) and oily mill scale free (OMS) using co-temporal methods and apparatus, including using equipment of the center «Ural-M», studied the physico-chemical properties of industrial wastes. The main components of RM are: Fe (35.7%) in the form of hematite and complex hydroalumination, Ca (11.0%) in the form of calcite and hydro-aluminosilicates, Al (6.8%) and Si (4.7%) in the composition of hydroalumination, Na (2.8%) in the form of hydroalumination, carbonate and hydroxide, Ti (2.5%) in the form of rutile. The sludge moisture content was 11.9%. The main components of the OMS are: Fe (71%) in the form of magnetite, wustite and hematite with a very small amount of fayalite. The contents of Si (in the form of quartz), Al and P (non-forming phases) are within 1-3%. Humidity OMS – 16.3%, the content of indelible organic matter – 4.0%. Granulometric composition of RM is characterized by high dispersion. With an average diameter of 1.6 µm, all particle sizes are in the range of 0.5-12 µm. Granulometric composition of OMS is characterized by complexity. With an average diameter of 8.6 µm, maxima of 0.9 µm and 15 µm and a minimum of about 1.2 µm are observed in the particle size distribution. The specific surface area of the materials is equal to RM 23.7 m2/g, and OMS – 1.9 m2/g. The change of waste properties after exposure to aqueous solutions of alkalis and acids neutralizing the effect of organic (OMS) and alkaline (RM) surface compounds was studied. Neutralization of aqueous sus¬pension with HCl solution leads to removal of alkaline film from the surface. As a result of the impact of reagents, there is a decrease in the content of water-soluble components in the processing products. At the same time, the average particle sizes of RM and OMS increase to 2 and 14 µm, respectively, and the specific surface area to 25.7 and 2.3 m2/g. The distribution of particle size of RM is almost constant, and the OMS is approximately 5 and 10% of the smoothed maximum and minimum in the area of at least 0.5 and 15 µm.

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