scholarly journals CCCM SPECIFIC SURFACE ESTIMATION IN PROCESS OF LOW-TEMPERATURE OXIDATION

2020 ◽  
Vol 17 (34) ◽  
pp. 793-802
Author(s):  
Veniamin A POGODIN ◽  
Alexey N ASTAPOV ◽  
Lev N RABINSKIY
Keyword(s):  
Low Temperature ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Fibers ◽  
Density Functional ◽  
Functional Model ◽  
Contact Boundary ◽  
Low Temperature Oxidation ◽  
Temperature Oxidation

The low-temperature oxidation process of carbon-carbon composite materials (CCCM) with a pyrocarbon matrix has been examined. Oxidation at temperatures of 450 to 700 °C is characterized by internal burnout of the carbon phase without a noticeable change in the experimental samples external volume. Oxidation resistance analysis of CCCM structural components was performed. CCCM and carbon fibers specific surface area were estimated by the low-temperature adsorption of nitrogen and krypton using the Brunauer-Emmett-Teller model and the theory of density functional model. Pore size distribution was calculated by the semi-empirical Horvath-Kawazoe method. A significant increase (about 10-15 times) in specific surface area of the composite material, together with a rise in free volume ~5%, was accompanied by total weight loss of about 5%. Specific surface area changes occur as a result of anisotropic etching of carbon fibers surface with the formation of micropores with 0.5–2.0 nm diameter range. Although macropores are formed mainly due to the oxidation of thermosetting binder pyrolysis residue, they do not contribute to the specific surface increase but solely provide access to micropores. Microporosity evolution leads to an increase of structural discontinuity degree and, ultimately, to the loss of matrix-filler contact boundary. As a result, an overall weakening of material mechanical characteristics is to be noted. Thus, oxidative degradation is closely related to the increase in void space. A follow-up study is on-going. In fact, an open question remains, namely whether the oxidative process occurs differently in the micropores of diameter less than 2 nm and how it may contribute to the oxidative stress resistance behavior of CCCM.

scholarly journals Characterization of Activated Carbon Fibers

1990 ◽  
Vol 209 ◽  
Author(s):  
A. W. P. Fung ◽  
A. M. Rao ◽  
K. Kuriyama ◽  
M. S. Dresselhaus ◽  
G. Dresseliiaus ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Low Temperature ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Fibers ◽  
Disordered Systems ◽  
Activated Carbon Fibers ◽  
Characterization Of Activated Carbon

AbstractLow-temperature electrical conductivity and Raman scattering are studied as characterization tools for activated carbon fibers, which have a high density of defects and a huge specific surface area. The transport mechanism at low temperature is governed by variablerange hopping, as in other strongly disordered systems. From the Raman spectra obtained, we deduce that the long phenolic fibers are more disordered than the acrylic fibers and that increased specific surface area corresponds to increased disorder. The average in-plane microcrystallite size is about 20–30 Å.

scholarly journals Time-Resolved X-ray Operando Observations of Lithiation Gradients across the Cathode Matrix and Individual Oxide Particles during Fast Cycling of a Li-Ion Cell

2021 ◽  
Author(s):  
Tianlong Zheng ◽  
Jing He ◽  
Pingwei Cai ◽  
Xi Liu ◽  
Duojie Wu ◽  
...  
Keyword(s):  
Electronic Structure ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
High Performance ◽  
Density Functional ◽  
Density Functional Theory Calculations ◽  
Carbon Paper ◽  
Free Energy Barrier ◽  
Active Components

Abstract Self-supporting three-dimensional (3D) transition metal electrodes have been considered for designing high-performance non-noble metal oxygen evolution reaction (OER) catalysts owing to their advantages such as binder-free, good mass transfer, and large specific surface area. However, the poor conductivity of ((oxy)hydr)oxides and the difficulty in adjusting their electronic structure limit their application. As an alternative strategy, instead of constituting the array electrode by the active components themselves, we herein report 3D Co(OH)2@MnO2 heterostructure decorated carbon nanoarrays grown directly on carbon paper (Co(OH)2@MnO2-CNAs). This unique structure can not only enhance electrical conductivity but also provide a larger specific surface area, and facilitate electrolyte diffusion and ion transport. The core-shell heterostructured Co(OH)2@MnO2 formed via incorporation with MnO2 facilitates the transition of CoII to CoIII in Co(OH)2 and it increases the storage of oxidative charge in the catalyst, leading to an OER activity with benchmark RuO2 and good stability. Density functional theory calculations suggest that the improved OER performance can be attributed to the formation of the heterojunction structure, resulting in the modulation of the electronic structure of Co atoms and the reduction of the free energy barrier of the rate-determining step for the OER.

scholarly journals Carbon fibers derived from pure alkali lignin fibers through electrospinning with carbonization

BioResources ◽  
2020 ◽  
Vol 15 (2) ◽  
pp. 2412-2427
Author(s):  
Tunnapat Worarutariyachai ◽  
Surawut Chuangchote
Keyword(s):  
Electrical Conductivity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Fibers ◽  
Smooth Surface ◽  
Synthetic Polymer ◽  
Inorganic Salts ◽  
Alkali Lignin ◽  
Surface Tension Reduction

Alkali lignin (AL) fibers with a smooth surface and fine morphological appearance were successfully produced via electrospinning using a simple heated single spinneret system, instead of typical electrospinning of lignin with added synthetic polymer blends or conventional co-axial electrospinning. To reduce the size of the fibers, glycerol was added to the spinning solution as a co-solvent for surface tension reduction and electrospinnability improvement. After electrospinning, stabilization and carbonization were subsequently performed to convert AL fibers to carbon fibers (CFs). The obtained CFs displayed rough and uneven surfaces. However, the CFs derived from glycerol-added solution showed greater electrical conductivity, specific surface area, and porosity compared with those from pure AL solution. Furthermore, the results indicated that the inorganic salts on the rough surface of CFs were successfully removed by sulfuric acid (H2SO4) washing. After H2SO4 washing, the CFs revealed a smoother surface and higher electrical conductivity, specific surface area, and porosity.

Modified polyacrylonitrile-based activated carbon fibers applied in supercapacitor

2016 ◽  
Vol 45 (3) ◽  
pp. 164-171 ◽  
Author(s):  
Linjie Su ◽  
Bohong Li ◽  
Dongyu Zhao ◽  
Chuanli Qin ◽  
Zheng Jin
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Specific Capacitance ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Fibers ◽  
Electrode Material ◽  
High Specific Capacitance ◽  
Activated Carbon Fibers ◽  
Content Type

Purpose The purpose of this paper is to prepare a new modified activated carbon fibers (ACFs) of high specific capacitance used for electrode material of supercapacitor. Design/methodology/approach In this study, the specific capacitance of ACF was significantly increased by using the phenolic resin microspheres and melamine as modifiers to prepare modified PAN-based activated carbon fibers (MACFs) via electrospinning, pre-oxidation and carbonization. The symmetrical supercapacitor (using MACF as electrode) and hybrid supercapacitor (using MACF and activated carbon as electrodes) were tested in term of electrochemical properties by cyclic voltammetry, AC impedance and cycle stability test. Findings It was found that the specific capacitance value of the modified fibers were increased to 167 Fg-1 by adding modifiers (i.e. 20 wt.% microspheres and 15 wt.% melamine) compared to that of unmodified fibers (86.17 Fg-1). Specific capacitance of modified electrode material had little degradation over 10,000 cycles. This result can be attributed to that the modifiers embedded into the fibers changed the original morphology and enhanced the specific surface area of the fibers. Originality/value The modified ACFs in our study had high specific surface area and significantly high specific capacitance, which can be applied as efficient and environmental absorbent, and advanced electrode material of supercapacitor.

scholarly journals Low-Temperature Synthesis of Monolithic Titanium Carbide/Carbon Composite Aerogel

Nanomaterials ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 2527
Author(s):  
Tingting Niu ◽  
Bin Zhou ◽  
Zehui Zhang ◽  
Xiujie Ji ◽  
Jianming Yang ◽  
...  
Keyword(s):  
Titanium Dioxide ◽  
Electron Microscope ◽  
Low Temperature ◽  
Titanium Carbide ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Composite ◽  
Composite Aerogel ◽  
X Ray

Resorcinol-formaldehyde/titanium dioxide composite (RF/TiO2) gel was prepared simultaneously by acid catalysis and then dried to aerogel with supercritical fluid CO2. The carbon/titanium dioxide aerogel was obtained by carbonization and then converted to nanoporous titanium carbide/carbon composite aerogel via 800 °C magnesiothermic catalysis. Meanwhile, the evolution of the samples in different stages was characterized by X-ray diffraction (XRD), an energy-dispersive X-ray (EDX) spectrometer, a scanning electron microscope (SEM), a transmission electron microscope (TEM) and specific surface area analysis (BET). The results showed that the final product was nanoporous TiC/C composite aerogel with a low apparent density of 339.5 mg/cm3 and a high specific surface area of 459.5 m2/g. Comparing to C aerogel, it could also be considered as one type of highly potential material with efficient photothermal conversion. The idea of converting oxide–carbon composite into titanium carbide via the confining template and low-temperature magnesiothermic catalysis may provide new sight to the synthesis of novel nanoscale carbide materials.

CVD Synthesis of Multi-Walled Carbon Nanotubes onto Different Catalysts at Low Temperature

NANO ◽  
2018 ◽  
Vol 13 (04) ◽  
pp. 1850036 ◽  
Author(s):  
Guiqiang Diao ◽  
Hao Li ◽  
Hao Liang ◽  
Iryna Ivanenko ◽  
Tetiana Dontsova ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
Low Temperature ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Sol Gel ◽  
Lithium Ion ◽  
Multi Walled Carbon Nanotubes ◽  
Walled Carbon Nanotubes

Multi-walled carbon nanotubes (MWCNTs) were synthesized onto a series of individual and bimetallic catalysts by the chemical vapor deposition (CVD) of acetylene at low temperature (600[Formula: see text]C). The catalysts were prepared by two methods, i.e., precipitation and sol–gel, with two different carriers – MgO and Al2O3. The catalysts were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermal gravimetric (TG) analysis, low-temperature adsorption of nitrogen. The yield of the MWCNTs was calculated in two ways, while the highest yield of 800% was achieved onto the two-component NiO/Co2O3/MgO catalyst, SEM and transmission electron microscopy (TEM) results confirm that uniform tube-like structure MWCNTs with the yield of 410% were obtained onto Co2O3/Al2O3 catalyst. These MWCNTs are smooth and pointing in the same direction. Their tube diameter is about 20[Formula: see text]nm, which is the smallest around all observed MWCNTs. Moreover, nonuniform curved bamboo-like MWCNTs with nozzles in the yield of 760% were obtained onto NiO/V2O3/MgO catalyst. Their diameter ranges from 25[Formula: see text]nm to 50[Formula: see text]nm. Results show that single-component catalyst promotes the growth of uniform and smaller nanotubes. Among the as-grown nanotubes, their specific surface area increases and average pores diameter reduces after the treatment with concentrated nitric acid at reflux and washing condition. The largest specific surface area (305[Formula: see text]m2/g) and average pores diameter (26[Formula: see text]m2/g) are processed to MWCNTs grown onto the NiO/Co2O3/MgO catalyst. MWCNTs with such large structural adsorption characteristics and purity of more than 99% obtained with yield 800% show potential use for preparation of nanocomposites as anode materials in lithium ion batteries.

scholarly journals Carbonate-Based Lanthanum Strontium Cobalt Ferrite (LSCF)–Samarium-Doped Ceria (SDC) Composite Cathode for Low-Temperature Solid Oxide Fuel Cells

2020 ◽  
Vol 10 (11) ◽  
pp. 3761
Author(s):  
Muhammed Ali S.A. ◽  
Jarot Raharjo ◽  
Mustafa Anwar ◽  
Deni Shidqi Khaerudini ◽  
Andanastuti Muchtar ◽  
...  
Keyword(s):  
Fuel Cells ◽  
Low Temperature ◽  
Solid Oxide Fuel Cells ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Composite Cathode ◽  
Solid Oxide ◽  
Oxide Fuel ◽  
Composite Electrolyte

Perovskite-based composite cathodes, La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF)–Ce0.8Sm0.2O1.9-carbonate (SDCC), were investigated as cathode materials for low-temperature solid-oxide fuel cells. The LSCF was mixed with the SDC–carbonate (SDCC) composite electrolyte at different weight percentages (i.e., 30, 40, and 50 wt %) to prepare the LSCF–SDCC composite cathode. The effect of SDCC composite electrolyte content on the diffraction pattern, microstructure, specific surface area, and electrochemical performances of the LSCF–SDCC composite cathode were evaluated. The XRD pattern revealed that the SDCC phase diffraction peaks vary according to its increasing addition to the system. The introduction of SDCCs within the composite cathode did not change the LSCF phase structure and its specific surface area. However, the electrical performance of the realized cell drastically changed with the increase of the SDCC content in the LSCF microstructure. This drastic change can be ascribed to the poor in-plane electronic conduction at the surface of the LSCF cathode layer due to the presence of the insulating phase of SDC and molten carbonate. Among the cathodes investigated, LSCF–30SDCC showed the best cell performance, exhibiting a power density value of 60.3–75.4 mW/cm2 at 600 °C to 650 °C.

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