• Carbon letters
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• v.16 no.1
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• pp.11-18
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• 2015

The process of oxidizing polyacrylonitrile (PAN)-based carbon fibers converts them into an infusible and non-flammable state prior to carbonization. This represents one of the most important stages in determining the mechanical properties of the final carbon fibers, but the most commonly used methods, such as thermal treatment ($200^{\circ}C$ to $300^{\circ}C$), tend to waste a great deal of process time, money, and energy. There is therefore a need to develop more advanced oxidation methods for PAN precursor fibers. In this review, we assess the viability of electron beam, gamma-ray, ultra-violet, and plasma treatments with a view to advancing these areas of research and their industrial application.

• Korean Journal of Materials Research
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• v.17 no.5
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• pp.278-282
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• 2007

Polyacrylonitrile nanofibers were fabricated by co-electrospinning technique and were characterized using scanning electron microscopy(SEM). We have evaluated systematically the effects of the important processing parameters affected on the morphology of the formed fibers; voltage, solution concentration and tip to collector distance. PAN nanofibers of about 200 nm${\sim}$2500 nm in diameter were well fabricated at the polymer concentration of 7.5 wt%${\sim}$15 wt%. It has been found that the average diameter of PAN nanofibers increased with increasing the concentration of PAN solution due to the reduction of whipping and splitting for the high viscosity solution. we also found an evidence that the applied voltage is strongly correlated with the distribution of nanofibers and the uniformed size of nanofibers were obtained at electrostatic value of 1 kV/cm.

• Macromolecular Research
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• v.14 no.3
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• pp.312-317
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• 2006

In the preparation of a polyacrylonitrile (PAN)/sodium montmorillonite (Na-MMT) nanocomposite via an in-situ polymerization method, macroazoinitiator (MAI) was intercalated in the gallery of Na-MMT to enhance the delamination of silicate layers by intergallery polymerization. The exfoliated fine dispersion observed by X-ray diffraction pattern and transmission electron microscopy, the enhanced tensile storage modulus and the thermal decomposition temperature showed that the intercalated MAI was effective in inducing intergallery polymerization and that a poly(ethylene glycol) block linked to a PAN block improved the dispersion of hydrophilic Na-MMT in the polymer matrix.

• Journal of the Korean Society for Heat Treatment
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• v.33 no.6
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• pp.290-295
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• 2020

In this study, Electro spinning was carried out using Cabon nanotube 0.1%-Polyacrylonitrile 3%-Dimethylformamide 17% agitation solution. It was investigated the solute and solvent correlations according to the electro spinning voltages ranging form 5 to 40 kV, based on the SEM image. Except voltage 25 kV, electro spinning was failed due to the lack of electro spinning (less than 60%). Voltage 25 kV was showed excellent properties, and was confirmed Cabon nanotube 58.1 nm and diameter of Cabon nanotube + Polyacrylonitrile 1.76 ㎛ as shown SEM image. Also, the tensile test results were showed that SK Chemical prepreg electro spinning angle of 0 and 90 degrees were 137 MPa and 60 MPa, respectively.

• Textile Coloration and Finishing
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• v.5 no.2
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• pp.144-148
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• 1993

To increase the moisture content and thereby to reduce the static charge of polyacrylonitrile (PAN), thin layer surface photografting of acylamide (AAm) onto PAN fabrics by using benzophenone as a initiator with a mixtured solvent was carried. The effects of reaction conditions such as monomer, initiator concentrations, UV irradiation time and immersion time of fabrics on grafting were investigated. The percent grafting slightly increased with increasing monomer concentration, benzophenone concentration up to limiting value and thereafter decreased or level offed. The percent grafting was significantly increased with increasing irradiation and immersion times. The moisture regain increased with increasing the percent grafting. The static charge decreased with increasing the percent grafting.

• Journal of Environmental Science International
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• v.25 no.12
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• pp.1613-1622
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• 2016

Zeolite (FZ), prepared from fly ash, was immobilized with polyacrylonitrile (PAN) to fabricate PAN/FZ beads. The prepared PAN/FZ beads were characterized by scanning electron microscopy, thermogravimetric analysis, and Fourier transform infrared spectroscopy. The optimum ratio to prepare PAN/FZ beads was 0.3 g of PAN to 0.3 g of FZ. The diameter of the prepared PAN/FZ beads was about 3 mm. Sr and Cu ion adsorption experiments were conducted with PAN/FZ beads. A pseudo-second-order model fit the kinetic data for Sr and Cu ion adsorption by PAN/FZ beads well. The equilibrium data fitted well with the Langmuir isotherm model, and the maximum adsorption capacities were 96.5 mg/g and 74.6 mg/g for the Sr and Cu ions, respectively. Additionally, the values of thermodynamic parameters such as Gibbs free energy (${\Delta}G^o$), enthalpy (${\Delta}H^o$) and entropy (${\Delta}S^o$) were determined. The positive values of ${\Delta}H^o$ revealed the endothermic nature of the adsorption process and the negative values of ${\Delta}G^o$ were indicative of the spontaneity of the adsorption process.

• Applied Chemistry for Engineering
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• v.34 no.2
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• pp.106-110
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• 2023

Lignin is compatible with various polymeric materials and useful as a carbon precursor. In this work, carbon monolith films were produced from polyacrylonitrile (PAN)@lignin precursor films by a controlled carbonization cycle. In addition, their morphological features, electrical properties, and adsorption behavior were analyzed and compared with those of carbonized PAN films. The successful formation of PAN@lignin precursor was confirmed by Fourier-transform infrared (FT-IR) spectroscopy. SEM was used to examine the morphology of precursor and carbonized films, revealing that both precursor and carbonized films retained structural stability following carbonization. A trace of lignin in the carbonized films was also found. The pore structure of the carbonized PAN@lignin film was measured using the BET method, indicating the formation of fairly uniform pores. The electrical properties were also analyzed to obtain the Ohmic relation, which demonstrated that the electrical signal was influenced by incoming materials. Finally, the carbonized PAN@lignin films were useful as adsorbents to remove metal ions. This study provides important information for future initiatives in relevant research fields.

• Carbon letters
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• v.12 no.3
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• pp.171-176
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• 2011

Polyacrylonitrile-based carbon nanofibers (CNFs) containing Ti and Mn were prepared by electrospinning. The effect of metal content on the hydrogen storage capacity of the nanofibers was evaluated. The nanofibers containing Ti and Mn exhibited maximum hydrogen adsorption capacities of 1.6 and 1.1 wt%, respectively, at 303 K and 9 MPa. Toward the development of an improved hydrogen storage system, the optimum conditions for the production of metalized CNFs were investigated by characterizing the specific surface areas, pore volumes, sizes, and shapes of the fibers. According to the results of Brunauer-Emmett-Teller analysis, the activation of the CNFs using potassium hydroxide resulted in a large pore volume and specific surface area in the samples. This is attributable to the optimized pore structure of the metal-containing polyacrylonitrile-based electrospun CNFs, which may provide better sites for hydrogen adsorption than do current adsorbates.

• Membrane Journal
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• v.27 no.3
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• pp.255-262
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• 2017

In this study, systematic integration of graphene oxide (GO) into polyacrylonitrile (PAN) nanofibers was accomplished by electrospinning to examine their mechanical properties. Exfoliated GO was initially prepared by the modified Hummer's method, and the surface of the GO was modified with an organic surfactant (e.g., cetyltrimetylammonium chloride) to improve its stability and dispersity. The overall mechanical property of the nanofiber composite membranes was highly improved. Particularly, the composite membranes with the modified GO exhibited much improved mechanical property, presumably due to the increased stability and dispersity of GO during electrospinning.

• Carbon letters
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• v.14 no.1
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• pp.45-50
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• 2013

Polyacrylonitrile (PAN) copolymers of different molecular weights were synthesized by a suspension polymerization and precipitation polymerization method. The rheology behaviors of the synthesized PAN copolymers were investigated in relation to their molecular weight, solid content and melting temperature. The influence of "historical effects" on the spinning solution of PAN was studied by analyzing the laws of viscosity considering the diversification time and temperature. The viscosity disciplines of each spinning solution conformed well to the rheological universal laws in a comparison of the suspension polymerization product with that of precipitation polymerization. Viscosity changes in the swelling process of dissolution were gentler in the suspension polymerization product; a small amount of water will quickly debase the solution viscosity, and high-speed mixing can greatly shorten the time required by the spinning solution to reach the final viscosity.