The Effect of Oxidation Temperature on Activating Commercial Viscose Rayon-Based Carbon Fibers to Make the Activated Carbon Fibers (ACFs)

2020 ◽  
Vol 985 ◽  
pp. 171-176
Author(s):  
Le Hoang Vu ◽  
Huu Son Nguyen ◽  
Quoc Khanh Dang ◽  
Van Cuong Pham ◽  
Thai Hung Le
Keyword(s):  
Carbon Dioxide ◽  
Activated Carbon ◽  
Surface Area ◽  
Carbon Fibers ◽  
Viscose Rayon ◽  
Bet Surface Area ◽  
Activated Carbon Fibers ◽  
Toxic Chemical ◽  
Viscose Fibers ◽  
Chemical Prevention

In this work, commercial Viscose (cellulosic based precursor) rayon-based carbon fibers were oxidized to make activated carbon fibers (ACFs). Carbon fibers were made from Viscose fibers in carbonization process at 1200°C. The ultimate carbon fibers possessed carbon content above 94 mass% and fiber dimension about 8 mm. These fibers were activated to make ACFs by oxidizing gas such as steam of carbon dioxide. The experiments were conducted at temperature ranged from 800°C to 900°C with carbonic steam’s flow of 3 l.min-1. The vaporous benzene adsorbability of activated carbon fibers was then measured by Mark Bell method. The adsorbability (a) and specific surface area (ABET) of ACFs were determined. The properties of the produced ACFs were investigated and analyzed by SEM and TEM imaging. The results showed that obtained fibers have maximum benzene adsorbability of 4.58 mmol.g-1 and BET surface area reached 1357 m2.g-1. These activated carbon fibers were able to use for toxic chemical prevention equipment.

scholarly journals Carbon Dioxide Adsorption on Porous and Functionalized Activated Carbon Fibers

2019 ◽  
Vol 9 (10) ◽  
pp. 1977 ◽  
Author(s):  
Yu-Chun Chiang ◽  
Cheng-Yu Yeh ◽  
Chih-Hsien Weng
Keyword(s):  
Carbon Dioxide ◽  
Activated Carbon ◽  
Surface Area ◽  
Carbon Fibers ◽  
Pore Volume ◽  
Co2 Adsorption ◽  
Physical Adsorption ◽  
Koh Activation ◽  
Co2 Uptake ◽  
Activated Carbon Fibers

Polyacrylonitrile-based activated carbon fibers (ACFs), modified using potassium hydroxide (KOH) or tetraethylenepentamine (TEPA), were investigated for carbon dioxide (CO2) adsorption, which is one of the promising alleviation approaches for global warming. The CO2 adsorption isotherms were measured, and the values of isosteric heat of adsorption were calculated. The results showed that the KOH-modified ACFs exhibited a great deal of pore volume, and a specific surface area of 1565 m2/g was obtained. KOH activation made nitrogen atoms easily able to escape from the surface of ACFs. On the other hand, the surface area and pore volume of ACFs modified with TEPA were significantly reduced, which can be attributed to the closing or blocking of micropores by the N-groups. The CO2 adsorption on the ACF samples was via exothermic reactions and was a type of physical adsorption, where the CO2 adsorption occurred on heterogeneous surfaces. The CO2 uptakes at 1 atm and 25 °C on KOH-activated ACFs reached 2.74 mmole/g. This study observed that microporosity and surface oxygen functionalities were highly associated with the CO2 uptake, implying the existence of O-C coordination, accompanied with physical adsorption. Well cyclability of the adsorbents for CO2 adsorption was observed, with a performance decay of less than 5% over up to ten adsorption-desorption cycles.

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 Photoconductivity of activated carbon fibers

1991 ◽  
Vol 6 (5) ◽  
pp. 1040-1047 ◽  
Author(s):  
K. Kuriyama ◽  
M.S. Dresselhaus
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Carbon Fibers ◽  
Low Temperatures ◽  
Room Temperature ◽  
High Surface ◽  
Localized States ◽  
Activated Carbon Fibers ◽  
Disordered Carbon ◽  
Increasing Temperature

The conductivity and photoconductivity are measured on a high-surface-area disordered carbon material, i.e., activated carbon fibers, to investigate their electronic properties. This material is a highly disordered carbon derived from a phenolic precursor, having a huge specific surface area of 1000–2000 m2/g. Our preliminary thermopower measurements show that the dominant carriers are holes at room temperature. The x-ray diffraction pattern reveals that the microstructure is amorphous-like with Lc ≃ 10 Å. The intrinsic electrical conductivity, on the order of 20 S/cm at room temperature, increases by a factor of several with increasing temperature in the range 30–290 K. In contrast, the photoconductivity in vacuum decreases with increasing temperature. The magnitude of the photoconductive signal was reduced by a factor of ten when the sample was exposed to air. The recombination kinetics changes from a monomolecular process at room temperature to a bimolecular process at low temperatures, indicative of an increase in the photocarrier density at low temperatures. The high density of localized states, which limits the motion of carriers and results in a slow recombination process, is responsible for the observed photoconductivity.

Activated carbon fiber from liquefied wood and polyvinyl butyral as an additive for production of flexible all-carbon yarn supercapacitors

Holzforschung ◽  
2018 ◽  
Vol 72 (5) ◽  
pp. 367-374 ◽  
Author(s):  
Yuxiang Huang ◽  
Wenji Yu ◽  
Guangjie Zhao
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Carbon Fibers ◽  
High Surface ◽  
High Surface Area ◽  
Polyvinyl Butyral ◽  
Activated Carbon Fiber ◽  
Bet Surface Area ◽  
Liquefied Wood ◽  
New Material

AbstractA novel way to prepare mesoporous activated carbon fibers (ACFs-P) has been developed, while the ACFs-P with high surface area were obtained from liquefied wood by combining polyvinyl butyral (PVB) blending and steam activation. The porosity properties of the new material was investigated by N2adsorption and the Brunauer–Emmett–Teller (BET) surface area was found to be 2710 m2g−1and a pore volume of 1.540 cm3g−1, of which 58.2% was mesoporous with diameters between 3 and 6 nm. ACFs-P had a higher methylene blue (MB) adsorption capacity (962 mg/g) than the PVB-added carbon fibers (CFs-P) and ACFs-P without PVB (ACFs-C). Flexible all-carbon yarn supercapacitors can be produced from ACFs-P as powder or fiber. The fiber approach led to yarn supercapacitors with a less favorable electrochemical performance than the powder based production owing to the poor strength of the fibers. A 10 cm long yarn supercapacitor from the powdered ACFs exhibited a high specific length capacitance of 43 mF cm−1at 2 mV s−1. Yarn supercapacitors showed an excellent mechanical flexibility and its capacitor properties were not diminished after bending or crumpling.

SURFACE PROPERTIES AND CATALYTIC PERFORMANCE OF ACTIVATED CARBON FIBERS SUPPORTED TiO2 PHOTOCATALYST

2008 ◽  
Vol 15 (04) ◽  
pp. 337-344 ◽  
Author(s):  
HUIFEN YANG ◽  
PINGFENG FU
Keyword(s):  
Activated Carbon ◽  
Carbon Fibers ◽  
Uv Light ◽  
Three Dimensional ◽  
Catalytic Performance ◽  
Dip Coating ◽  
Bet Surface Area ◽  
Activated Carbon Fibers ◽  
Organic Silicon ◽  
Acrylate Copolymer

Activated carbon fibers supported TiO 2 photocatalyst ( TiO 2/ACF) in felt-form was successfully prepared with a dip-coating process using organic silicon modified acrylate copolymer as a binder followed by calcination at 500°C in a stream of Ar gas. The photocatalyst was characterized by SEM, XRD, XPS, FTIR, and BET surface area. Most of carbon fibers were coated with uniformly distributed TiO 2 clusters of nearly 100 nm. The loaded TiO 2 layer was particulate for the organic binder in the compact film was carbonized. According to XPS and FTIR analysis, amorphous silica in carbon grains was synthesized after carbonizing organic silicon groups, and the Ti – O – Si bond was formed between the interface of loaded TiO 2 and silica. Additionally, the space between adjacent carbon fibers still remained unfilled after TiO 2 coating, into which both UV light and polluted solutions could penetrate to form a three-dimensional environment for photocatalytic reactions. While loaded TiO 2 amount increased to 456 mg TiO 2/1 g ACF, the TiO 2/ACF catalyst showed its highest photocatalytic activity, and this activity only dropped about 10% after 12 successive runs, exhibiting its high fixing stability of coated TiO 2.

Preparation and Characterization of Fibrous Cerium Oxide Templated from Activated Carbon Fibers

2005 ◽  
Vol 876 ◽  
Author(s):  
Mark Crocker ◽  
Uschi M. Graham ◽  
Rolando Gonzalez ◽  
Erin Morris ◽  
Gary Jacobs ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Cerium Oxide ◽  
Carbon Fibers ◽  
High Surface ◽  
Nitrate Solution ◽  
High Surface Area ◽  
Cerium Nitrate ◽  
Activated Carbon Fibers ◽  
Templating Method

AbstractHigh surface area cerium oxide has been prepared using a carbon templating method. Impregnation of a highly mesoporous activated carbon (Darco KB-B) with an aqueous solution of cerium nitrate, followed by carbon burn off, afforded ceria with surface area of up to 148 m2/g. According to thermogravimetric studies, ceria formation proceeds via decomposition of cerium nitrate at ca. 410 K; oxidation of the carbon template commences at the same temperature, being facilitated by the release of NO2 from the Ce compound. Use of activated carbon fibers (ACFs) as template was found to provide a simple route to fibrous cerium oxide. The lower surface areas (3 - 59 m2/g) of the resulting ceria fibers reflect the largely microporous nature of the ACFs; evidently the Ce nitrate solution is unable to penetrate their micropores. Consequently, the surface area of the ceria product is found to increase with increasing mesoporosity of the ACF template. Electron microscopy reveals that the ceria fibers are composed of highly crystalline primary particles of 5-10 nm diameter; further, the fibers display a number of interesting morphological features at the macro- and nano-scales.

Fabrication of Activated Carbon Fibers from Stabilized PAN-Based Fibers by KOH

2004 ◽  
Vol 449-452 ◽  
pp. 217-220 ◽  
Author(s):  
Young Jae Lee ◽  
Jae Hyung Kim ◽  
Jang Soon Kim ◽  
Dong Bok Lee ◽  
Jae Chun Lee ◽  
...  
Keyword(s):  
Experimental Data ◽  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Fibers ◽  
Potassium Hydroxide ◽  
Chemical Activation ◽  
Activated Carbon Fibers ◽  
High Concentration

Activated carbon fibers were prepared from stabilized PAN-based fibers by chemical activation using potassium hydroxide at different concentration. The experimental data showed variations in specific surface area, microstructure by the activated carbon fibers. Specific surface area of about 2545 m2/g was obtained in the KOH/stabilized PAN-based fiber ratio of 1:1 at 800°. An abrupt reduction of specific surface area was observed in the experiments with the ratio of 3:1 of OH/stabilized PAN-based fiber, being dissimilar with the result of KOH/fiber ratios of 1:1 and 2:1 in the similar experiments. The high concentration of KOH led to the destruction of micropore walls instead of forming mesopores.

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