연구에서는, 전기방사법을 이용하여 산화철-산화그래핀(Fe3O4/GO, metallic graphene oxide; MGO)이 도입된 PVdF/MGO 복합나노섬유(PMG)를 제조하였으며, 이를 활용하여 비소제거에 대한 특성 평가를 진행하였다. MGO의 경우 In-situ-wet chemical 방법으로 제조하였으며, FT-IR, XRD분석을 진행하여, 형태와 구조를 확인하였다. 나노섬유 분리막의 기 계적 강도 개선을 위하여 열처리과정을 진행하였으며, 제조된 분리막의 우수한 기계적 강도 개선 효과를 확인할 수 있었다. 그러나, PMG 막의 경우, 도입된 MGO의 함량이 증가할수록 기계적 강도가 감소되는 경향성을 보여주었으며, 기공크기 분석 결과로부터, 0.3~0.45 μm의 기공크기를 가진 다공성 분리막이 제조되었음을 확인할 수 있었다. 수처리용 분리막으로의 활용 가능성 조사를 위해, 수투과도 분석을 실시하였다. 특히, PMG2.0 샘플의 경우 0.3 bar 조건에서, PVdF 나노섬유막(91 kg/m2h)에 비해 약 70% 향상된 결과값(153 kg/m2h)을 나타내었다. 또한, 비소 흡착실험 결과로부터, PMG 막의 경우, 비소3 가와 5가에 최대 81%, 68%의 높은 제거율을 보여주었으며, 흡착등온선 분석으로부터, 제조된 PMG 막의 경우 비소3가, 5가 모두 Freundlich 흡착거동을 따른다는 것을 확인하였다. 위 모든 결과로부터, PVdF/MGO 복합 나노섬유 분리막은 비소제거 및 수처리용 분리막으로 충분히 활용할 수 있을 것으로 판단된다.

The uniform nanofibers of polyurethane with different contents of Juniperus Chinensis extracts were successfully prepared by electrospinning method. Polyurethane is widely used as functional polymers in the industrials, medical field as their properties can be tailor-made by adjusting their compositions. Juniperus Chinensis has been reported for anti-tumor, anti-bacterial, anti-fungal, and anti-viral activities. PU/Juniperus Chinensis extracts composite nanofibers were produced at different Juniperus Chinensis extracts concentrations (0.25, 0.5, 1, 1.5wt.%). The effects of the major parameters in electrospinning process such as tip to collector distance (TCD), voltage, polymer concentration on the average diameter of electrospun nanoweb were investigated. As results, 12wt% PU solution concentration, 8kV applied voltage and 15cm tip to collector distance were identified as optimum conditions for electrospinning the composite nanofibers. The diameter and morphology of the nanocomposite nanofibers were confirmed by a scanning electron microscopy (SEM). The resulting fibers exhibited a uniform diameter ranging from 435nm∼547nm. It has been found that the average diameters of fibers decreased by the adding of Juniperus Chinensis extracts. These nanowebs can be used for medical materials, protective clothing, and antimicrobial filters.

본 연구에서는, 전기방사를 위하여 알지네이트와 키토산을 이용하여 알지네이트/poly(ethylene oxide)(PEO)와 키 토산/PEO 용액을 준비하였다. 준비된 용액을 10 mL 플라스틱 주사기에 넣고 금속 노즐에 높은 전압을 공급하였다. 키토산과 알지네이트 용액은 고분자 농도, 온도, 상대습도, 인가전압, 노즐과의 거리, 그리고 용액 속도에 의해 컨트롤되었다. 제조된 나노섬유막은 전자주사현미경을 이용하여 모폴로지를 관찰하였다. 알지네이트 전기방사를 위한 나노 섬유막의 최적화된 조건 은 2 wt% 알지네이트, 2 wt% PEO, 60°C, 노즐과의 거리 15 cm, 20~24 kV, 8 μm/min이었으며, 키토산 섬유막의 최적화 조 건은 2 wt% 키토산, 2 wt% PEO, 25°C, 노즐과의 거리 15 cm, 24 kV, 8 μm/min이었다. 복합 나노섬유 제조조건은 노즐과의 거리 20 cm, 8 μm/min, 26 kV이었다.

Novel processable sulfur copolymer (poly(S-r-CEA)) was synthesized via facile inverse vulcanization of elemental sulfur with 2-carboxyethyl acrylate (CEA). This polysulfide was electrospun producing sulfur-rich nanofiber and tested for heavy metal sequestration. Adsorption experiments show very high and efficient Hg2+ adsorption. This work extends the novelty of inverse vulcanization chemistry by developing method for preparation of material based on inverse vulcanized polysulfide. Consequently, a new and cheap yet effective material was prepared for heavy metal sequestration from contaminated water. This work was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (2015R1A2A1A15055407) and by the Ministry of Education (No. 2009-0093816).

전기방사를 사용하여 제조된 나노섬유의 활용은 필터분야, 보호 의류 분야, 에너지 저장기능분야 등 다양한 분야가 있다. 이에 본 연구에서는 우수한 물성을 가지는 polybenzimidazole을 이용하여 방사 용액의 농도, 인가 전압, 방사 거리, collector speed에 따라 방사를 진행하였고, 후처리 과정까지 연구해보았다. 각각의 변수에 따라 nanofiber의 형태, sheet의 기계적 물성 등의 특성을 평가하였으며, 분리막 분야에 적용 가능한 적합한 방사조건에 대하여 연구하였다.

생체적합성과 흡습 특성이 있는 polyamide6 (PA6)를 혈액투석용 분리막으로 사용하기 위해 16 wt% PA6 고분자 용액을 전기방사하여 제조하였다. 제조된 PA6 nanofiber membrane은 직경(fiber diameter), 표면특성, 기공의 크기 분석을 통해 혈액투석용 분리막으로 최적화하였다. PA6 nanofiber membrane는 제 올라이트가 첨가된 친수성 고분자 용액으로 개질하여 혈액 속 노폐물인 creatinine 흡착 제거용 분리막으로 사용하고, creatine의 흡착효과는 UV-visible 분석으로 확인하였다.

The development of glucose biosensors has been attracting much attention because of their importance in monitoring glucose in the human body; such sensors are used to diagnose diabetes and related human diseases. Thanks to the high selectivity, sensitivity to glucose detection, and relatively low-cost fabrication of enzyme-immobilized electrochemical glucose sensors, these devices are recognized as one of the most intensively investigated glucose sensor types. In this work, ZnO nanofibers were synthesized using an electrospinning method with polyvinyl alcohol zinc acetate as precursor material. Using the synthesized ZnO nanofibers, we fabricated glucose biosensors in which glucose oxidase was immobilized on the ZnO nanofibers. The sensors were used to detect a wide range of glucose from 10 to 700 M with a sensitivity of 10.01 nA/cm2- μM, indicating that the ZnO nanofiber-based glucose sensor can be used for the detection of glucose in the human body. The control of nanograins in terms of the size and crystalline quality of the individual nanofibers is required for improving the glucose-sensing abilities of the nanofibers.

Zein/Poria cocos extract nanofibers were prepared based on the electrospinning of aqueous solutions with different Poria cocos extract concentrations (0, 5, 10, and 15 wt.%). The electrospinning parameters, including the polymer contents, voltage, and tip-to-collector distance (TCD), were optimized for the fabrication process. The resulting electrospun materials were all characterized using field-emission scanningelectron microscopy (FE-SEM). The diameters of the electrospun zein nanofibers were found to increase when increasing the zein concentration.

Membrane distillation (MD) has emerged as a next generation of desalination technique to resolve the limitation of RO process. In this study, Polybenzoxazoles(PBO) membrane via thermally rearrangement of polyimide containing hydroxyl groups was prepared [1]. The effect of operating conditions such as feed temperature, Reynolds number of feed flow and salt concentration of feed were investigated. TR polymer membranes were characterized by SEM, AFM and contact angle. Thermally rearranged polymers showed a potential to MD process with advantages of high flux and long-term stability during operation.

본 연구에서는 백혈구 친화 흡착 및 분리 가능한 기능성 필터를 개발하기 위해, 직경이 3μm이하를 가지는 부직포 표면에 전기 방사법을 이용하여 평막형태의 혈액분리용 필터를 제조하였다. 전기방사는 고분자 농도, 유량, 인가전압, 에어갭 등의 변수를 조절하여 나노/마이크로 구조를 최적화하였다. 분리막의 단면과 표면 모폴로지는 전계방출형주사현미경(FE-SEM)을 이용하여 관찰하였다. 화학적 표면처리를 통해 친수성을 증가시켰으며, 혈액적합성 평가결과 우수한 것을 확인 할 수 있었다.

Sb-doped SnO2(ATO) thin films were prepared using electrospinning. To investigate the optimum properties of the electrospun ATO thin films, the deposition numbers of the ATO nanofibers(NFs) were controlled to levels of 1, 2, 4, and 6. Together with the different levels of deposition number, the structural, chemical, morphological, electrical, and optical properties of the nanofibers were investigated. As the deposition number of the ATO NFs increased, the thickness of the ATO thin films increased and the film surfaces were gradually densified, which affected the electrical properties of the ATO thin films. 6 levels of the ATO thin film exhibited superior electrical properties due to the improved carrier concentration and Hall mobility resulting from the increased thickness and surface densification. Also, the thickness of the samples had an effect on the optical properties of the ATO thin films. The ATO thin films with 6 deposited levels displayed the lowest transmittance and highest haze. Therefore, the figure of merit(FOM) considering the electrical and optical properties showed the best value for ATO thin films with 4 deposited levels.

We synthesized Fe-doped TiO2/α-Fe2O3 core-shell nanowires(NWs) by means of a co-electrospinning method anddemonstrated their magnetic properties. To investigate the structural, morphological, chemical, and magnetic properties of thesamples, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectronspectroscopy were used, as was a vibrating sample magnetometer. The morphology of the nanostructures obtained aftercalcination at 500oC exhibited core/shell NWs consisting of TiO2 in the core region and α-Fe2O3 in the shell region. In addition,the XPS results confirmed the formation of Fe-doped TiO2 by the doping effect of Fe3+ ions into the TiO2 lattice, which canaffect the ferromagnetic properties in the core region. For comparison, pure α-Fe2O3 NWs were also fabricated using anelectrospinning method. With regard to the magnetic properties, the Fe-doped TiO2/α-Fe2O3 core-shell NWs exhibited improvedsaturation magnetization(Ms) of approximately ~2.96emu/g, which is approximately 6.1 times larger than that of pure α-Fe2O3NWs. The performance enhancement can be explained by three main mechanisms: the doping effect of Fe ions into the TiO2lattice, the size effect of the Fe2O3 nanoparticles, and the structural effect of the core-shell nanostructures.

Spinnable pitch for melt-electrospinning was obtained from pyrolized fuel oil by electron beam (E-beam) radiation treatment. The modifiedpitch was characterized by measuring its elemental composition, softening point, viscosity, molecular weight, and spinnability. The softening point and viscosity properties of the modifiedpitch were influencedby reforming types (heat or E-beam radiation treatment) and the use of a catalyst. The softening point and molecular weight were increased in proportion to absorbed doses of E-beam radiation and added AlCl3 due to the formation of pitch by free radical polymerization. The range of the molecular weight distribution of the modifiedpitch becomes narrow with better spinning owing to the generated aromatic compounds with similar molecular weight. The diameter of melt-electrospun pitch fibersunder applied power of 20 kV decreased 53% (4.7 ± 0.9 μm) compared to that of melt-spun pitch fibers(10.2 ± 2.8 μm). It is found that E-beam treatment for reforming could be a promising method in terms of time-savings and cost-effectiveness, and the melt-electrospinning method is suitable for the preparation of thinner fibersthan those obtained with the conventional melt-spinning method.

Flake-like LiCoO2 nanopowders were fabricated using electrospinning. To investigate their formation mech-anism, field-emssion scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy were carriedout. Among various parameters of electrospinning, we controlled the molar concentration of the precursor and the PVPpolymer. When the molar concentration of lithium and cobalt was 0.45 M, the morphology of LiCoO2 nanopowders wasirregular and round. For 1.27 M molar concentration, the LiCoO2 nanopowders formed with flake-like morphology. Forthe PVP polymer, the molar concentration was set to 0.011 mM, 0.026 mM, and 0.043 mM. Irregular LiCoO2 nanop-owders were formed at low concentration (0.011 mM), while flake-like LiCoO2 were formed at high concentration(0.026 mM and 0.043 mM). Thus, optimized molar concentration of the precursor and the PVP polymer may be relatedto the successful formation of flake-like LiCoO2 nanopowders. As a results, the synthesized LiCoO2 nanopowder can beused as the electrode material of Li-ion batteries.

Carbon nanofibers (CNFs) with diameters in the submicron and nanometer range exhibit high specific surface area, hierarchically porous structure, flexibility, and super strength which allow them to be used in the electrode materials of energy storage devices, and as hybrid-type filler in carbon fiber reinforced plastics and bone tissue scaffold. Unlike catalytic synthesis and other methods, electrospinning of various polymeric precursors followed by stabilization and carbonization has become a straightforward and convenient way to fabricate continuous CNFs. This paper is a comprehensive and brief review on the latest advances made in the development of electrospun CNFs with major focus on the promising applications accomplished by appropriately regulating the microstructural, mechanical, and electrical properties of as-spun CNFs. Additionally, the article describes the various strategies to make a variety of carbon CNFs for energy conversion and storage, catalysis, sensor, adsorption/separation, and biomedical applications. It is envisioned that electrospun CNFs will be the key materials of green science and technology through close collaborations with carbon fibers and carbon nanotubes.

Photoelectrochemical cells have been used in photolysis of water to generate hydrogen as a clean energy source. A high efficiency electrode for photoelectrochemical cell systems was realized using a ZnO hierarchical nanostructure. A ZnO nanofiber mat structure was fabricated by electrospinning of Zn solution on the substrate, followed by oxidation; on this substrate, hydrothermal synthesis of ZnO nanorods on the ZnO nanofibers was carried out to form a ZnO hierarchical structure. The thickness of the nanofiber mat and the thermal annealing temperature were determined as the parameters for optimization. The morphology of the structures was examined by field-emission scanning electron microscopy, transmission electron microscopy, and X-ray diffraction. The performance of the ZnO nanofiber mat and the potential of the ZnO hierarchical structures as photoelectrochemical cell electrodes were evaluated by measurement of the photoelectron conversion efficiencies under UV light. The highest photoconversion efficiency observed was 63 % with a ZnO hierarchical structure annealed at 400˚C in air. The morphology and the crystalline quality of the electrode materials greatly influenced the electrode performance. Therefore, the combination of the two fabrication methods, electrospinning and hydrothermal synthesis, was successfully applied to fabricate a high performance photoelectrochemical cell electrode.

To investigate the effects of co-solvents on the morphology of nano-scale zein materials, zein solutions were electrospun with different co-solvent ratios of EtOH/H2O. Different zein solution concentrations were used to study the effects of the zein content on the electrospun materials. The resulting electrospun materials were all characterized using field-emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). The diameters of the electrospun nanoparticles and nanofibers were found to increase when increasing the EtOH ratio at certain zein concentrations. Furthermore, increasing the zein content changed the morphology of the electrospun materials from nanoparticles to nanofibers.

Well-distributed SnO2-Sn-Ag3Sn nanoparticles embedded in carbon nanofibers were fabricated using a co-electrospinning method, which is set up with two coaxial capillaries. Their formation mechanisms were successfully demonstrated. The structural, morphological, and chemical compositional properties were investigated by field-emission scanning electron spectroscopy (FESEM), bright-field transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). In particular, to obtain well-distributed SnO2 and Sn and Ag3Sn nanoparticles in carbon nanofibers, the relative molar ratios of the Ag precursor to the Sn precursor including 7 wt% polyacrylonitrile (PAN) were controlled at 0.1, 0.2, and 0.3. The FESEM, bright-field TEM, XRD, and XPS results show that the nanoparticles consisting of SnO2-Sn-Ag3Sn phases were in the range of ~4 nm-6 nm for sample A, ~5 nm-15 nm for sample B, ~9 nm-22 nm for sample C. In particular, for sample A, the nanoparticles were uniformly grown in the carbon nanofibers. Furthermore, when the amount of the Ag precursor and the Sn precursor was increased, the inorganic nanofibers consisting of the SnO2-Sn-Ag3Sn nanoparticles were formed due to the decreased amount of the carbon nanofibers. Thus, well-distributed nanoparticles embedded in the carbon nanofibers were successfully synthesized at the optimum molar ratio (0.1) of the Ag precursor to the Sn precursor after calcination of 800˚C.

Metal nanowires can be coated on various substrates to create transparent conducting films that can potentially replace the dominant transparent conductor, indium tin oxide, in displays, solar cells, organic light-emitting diodes, and electrochromic windows. One issue with these metal nanowire based transparent conductive films is that the resistance between the nanowires is still high because of their low aspect ratio. Here, we demonstrate high-performance transparent conductive films with silver nanofiber networks synthesized by a low-cost and scalable electrospinning process followed by two-step sequential thermal treatments. First, the PVP/AgNO3 precursor nanofibers, which have an average diameter of 208 nm and are several thousands of micrometers in length, were synthesized by the electrospinning process. The thermal behavior and the phase and morphology evolution in the thermal treatment processes were systematically investigated to determine the thermal treatment atmosphere and temperature. PVP/AgNO3 nanofibers were transformed stepwise into PVP/Ag and Ag nanofibers by two-step sequential thermal treatments (i.e., 150˚C in H2 for 0.5 h and 300˚C in Ar for 3 h); however, the fibrous shape was perfectly maintained. The silver nanofibers have ultrahigh aspect ratios of up to 10000 and a small average diameter of 142 nm; they also have fused crossing points with ultra-low junction resistances, which result in high transmittance at low sheet resistance.

nanotubes were successfully synthesized using an electrospinning technique followed by calcination in air. The nanotubes were the single phase nature of and consisted of approximately 14 nm nanocrystals. SEM and TEM characterizations demonstrated that uniform hollow fibers with an average outer diameter of around 124 nm and wall thickness of around 25 nm were successfully obtained. As anode materials for lithium ion batteries, the nanotubes exhibited excellent cyclability and reversible capacity of up to 25 cycles at as compared to nanoparticles with a capacity of . Such excellent performance of the nanotube was related to the one-dimensional hollow structure which acted as a buffer zone during the volume contraction and expansion of Sn.