The significance of this study lies in addressing critical issues prevalent in the worldwide construction sector, particularly concerning the durability and sustainability of cement-based materials. Plain cement composites commonly suffer from deficiencies in tensile strength and strain capacity, resulting in the formation of nano-cracks under relatively low tensile loads. These nano- cracks pose a significant challenge to the longevity and resilience of cement matrices, contributing to structural degradation and reduced service life of infrastructure. To mitigate these challenges, the integration of cellulose nanofibers (CNF) as reinforcements in cement composites presents a promising solution. CNF, renowned for their exceptional material properties including high stiffness, tensile strength, and corrosion resistance, offer the potential to significantly enhance the mechanical performance and durability of cement-based materials. Through systematic experimentation, this study investigates the effects of CNF reinforcement on the mechanical properties of cement composites. By leveraging ultrasonically dispersion techniques, CNF extracted from bamboo, broad leaf, and kenaf are uniformly dispersed within the cement matrix at varying concentrations. Compressive and flexural tests are subsequently conducted to evaluate the impact of CNF on the strength characteristics of the cement composites. By elucidating the efficacy of CNF reinforcement through rigorous experimentation, this study aims to provide valuable insights into the development of construction materials with improved durability and sustainability. Ultimately, this research contributes to addressing critical challenges in the construction industry, offering potential solutions to enhance the performance and longevity of cement-based infrastructure.

Carbon nanofibers (CNFs) are promising materials for the construction of energy devices, particularly organic solar cells. In the electrospinning process, polyacrylonitrile (PAN) has been utilized to generate nanofibers, which is the simplest and most popular method of creating carbon nanofibers (CNFs) followed by carbonization. The CNFs are coated on stainless steel (SS) plates and involve an electropolymerization process. The prepared Cu, CNF, CNF–Cu, PANI, PANI–Cu, CNF–PANI, and CNF–PANI–Cu electrode materials’ electrical conductivity was evaluated using cyclic voltammetry (CV) technique in 1 M H2SO4 electrolyte solution. Compared to others, the CNF–PANI–Cu electrode has higher conductivity that range is 3.0 mA. Moreover, the PANI, CNF–PANI, and CNF–PANI–Cu are coated on FTO plates and characterized for their optical properties (absorbance, transmittance, and emission) and electrical properties (CV and Impedance) for organic solar cell application. The functional groups, and morphology-average roughness of the electrode materials found by FT–IR, XRD, XPS, SEM, and TGA exhibit a strong correlation with each other. Finally, the electrode materials that have been characterized serve to support and act as the nature of the hole transport for organic solar cells.

In this study, a milled carbon nanofiber-reinforced composite paint was prepared to enhance the anti-corrosive properties of concrete structures. Shorter-length (40 μm) milled carbon fibers (MCFs) showed an increased viscosity relative to longer MCFs (120 μm) owing to their 2 weeks (the decrease was especially strong in the acid solution). A carbon nanotube (CNT)- reinforced composite paint showed similar results in uniform distribution in the epoxy resin. The latter showed a decrease in viscosity owing to agglomerative movement in the epoxy resin. The surface hardness and tensile strength of the composite paint linearly increased as the carbon nanofiber loading was increased by up to 7.2 wt% in the epoxy resin, and slowly decreased after soaking in a sulfuric acid or sodium hydroxide solution for to those of the MCFs, whereas CNTs dispersed in isopropyl alcohol (IPA) in advance and mixed with resin showed lower hardness values than those without dispersion in IPA at the same loading. The mechanical properties such as the Shore D hardness and tensile strength of the MCF-reinforced composite paint increased significantly, resulting in a slower surface degradation of the composite paint concrete in a sulfuric acid and sodium hydroxide solution.

In this study, we have fabricated the phenolic resin (PR)/polyacrylonitrile (PAN) blend-derived core-sheath nanostructured carbon nanofibers (CNFs) via one-pot solution electrospinning. The obtained core-sheath nanostructured carbon nanofibers were further treated by mixed salt activation process to develop the activated porous CNFs (CNF-A). Compared to pure PAN-based CNFs, the activated PR/PAN blend with PR 20% (CNF28-A)-derived core-sheath nanostructured CNFs showed enhanced specific capacitance of ~ 223 F g− 1 under a three-electrode configuration. Besides, the assembled symmetric CNF28-A//CNF28-A device possessed a specific capacitance of 76.7 F g− 1 at a current density of 1 A g− 1 and exhibited good stability of 111% after 5,000 galvanostatic charge/discharge (GCD) cycles, which verifies the outstanding long-term cycle stability of the device. Moreover, the fabricated supercapacitor device delivered an energy density of 8.63 Wh kg− 1 at a power density of 450 W kg− 1.

Energy storage systems should address issues such as power fluctuations and rapid charge-discharge; to meet this requirement, CoFe2O4 (CFO) spinel nanoparticles with a suitable electrical conductivity and various redox states are synthesized and used as electrode materials for supercapacitors. In particular, CFO electrodes combined with carbon nanofibers (CNFs) can provide long-term cycling stability by fabricating binder-free three-dimensional electrodes. In this study, CFO-decorated CNFs are prepared by electrospinning and a low-cost hydrothermal method. The effects of heat treatment, such as the activation of CNFs (ACNFs) and calcination of CFO-decorated CNFs (C-CFO/ACNFs), are investigated. The C-CFO/ACNF electrode exhibits a high specific capacitance of 142.9 F/g at a scan rate of 5 mV/s and superior rate capability of 77.6% capacitance retention at a high scan rate of 500 mV/s. This electrode also achieves the lowest charge transfer resistance of 0.0063 Ω and excellent cycling stability (93.5% retention after 5,000 cycles) because of the improved ion conductivity by pathway formation and structural stability. The results of our work are expected to open a new route for manufacturing hybrid capacitor electrodes containing the C-CFO/ACNF electrode that can be easily prepared with a low-cost and simple process with enhanced electrochemical performance.

본 연구에서는 polyketone (PK)을 이용하여 전기방사 조건에 따른 섬유 형상의 특성 변화와 유수분리 가능성을 확인해 보았다. 고습과 저습 조건에서는 마이크론 직경의 섬유가 형성되었으며, 특히 고습에서는 섬유의 표면이 거칠게 변한 것이 확인되었다. 섬유 직경을 micro에서 nano로 변경하기 위하여 방사용액에 염을 추가하였으며, 그 결과 섬유 직경이 약 90% 감소하는 것을 확인할 수 있었다. 제조된 rPK-LNC와 PK-H로 유수분리 특성을 확인하기 위해 oil/water 에멀션으로 중 력 조건에서 유수분리를 진행하였으며 total organic carbon (TOC)와 탁도를 측정하여 특성을 분석하였다. 제거율 확인결과 탁도가 TOC와 동일한 경향성을 나타내는 것이 확인되었다. 따라서 본 연구에서는 고분자의 방사조건과 염의 유무에 따른 분리막의 섬유 형상과 물리적 특성변화와 이를 이용한 유수분리 특성에 대해 연구하였다.

급격한 산업화와 인구수 증가로 인한 환경 수질 오염이 발생하고 있다. 더불어 날씨 패턴의 변화로 인해 빗물이 부족해지자, 폐수를 깨끗한 물로 재활용하기 위한 요구가 나날이 늘어나고 있다. 색변화를 이용한 수중 속 중금속 검출은 아주 간단하고 효과적인 기술이다. 본 논문에는 멤브레인을 이용한 수은 이온 색검출에 대해 자세하게 논의되어 있다. 셀룰로 스, 폴리카프로락톤, 키토산, 폴리설폰 등의 멤브레인이 금속 이온 검출을 지지체로서 사용되었다. 지지체로서 사용된 멤브레 인들은 나노 섬유를 기반으로 하며 표면적이 크며, 중금속 검출의 활성 부위로 사용하기에 탁월하다. 나노 섬유를 기반으로 한 재료는 에너지, 환경, 그리고 바이오메디컬 연구에서 다양하게 응용될 수 있다. 나노 섬유로 이루어진 멤브레인들은 폴리머에 있는 적용기를 많이 받아들일 수 있으며, 표면적이 넓고 다공성이라는 장점이 있다. 이로 인해 멤브레인의 표면 구조를 변화시키거나 리간드를 섬유 표면에 부착해 나노 입자 결합을 더 쉽게 해준다.

Bismuth vanadate (BiVO4) is considered a potentially attractive candidate for the visible-light-driven photodegradation of organic pollutants. In an effort to enhance their photocatalytic activities, BiVO4 nanofibers with controlled microstructures, grain sizes, and crystallinities are successfully prepared by electrospinning followed by a precisely controlled heat treatment. The structural features, morphologies, and photo-absorption performances of the asprepared samples are systematically investigated and can be readily controlled by varying the calcination temperature. From the physicochemical analysis results of the synthesized nanofiber, it is found that the nanofiber calcines at a lower temperature, shows a smaller crystallite size, and lower crystallinity. The photocatalytic degradation of rhodamine-B (RhB) reveals that the photocatalytic activity of the BiVO4 nanofibers can be improved by a thermal treatment at a relatively low temperature because of the optimization of the conflicting characteristics, crystallinity, crystallite size, and microstructure. The photocatalytic activity of the nanofiber calcined at 350oC for the degradation of RhB under visible-light irradiation exhibits a greater photocatalytic activity than the nanofibers synthesized at 400oC and 450oC.

To meet the current demand in the fields of permanent magnets for achieving a high energy density, it is imperative to prepare nano-to-microscale rare-earth-based magnets with well-defined microstructures, controlled homogeneity, and magnetic characteristics via a bottom-up approach. Here, on the basis of a microstructural study and qualitative magnetic measurements, optimized reduction conditions for the preparation of nanostructured Sm-Co magnets are proposed, and the elucidation of the reduction-diffusion behavior in the binary phase system is clearly manifested. In addition, we have investigated the microstructural, crystallographic, and magnetic properties of the Sm-Co magnets prepared under different reduction conditions, that is, H2 gas, calcium, and calcium hydride. This work provides a potential approach to prepare high-quality Sm-Co-based nanofibers, and moreover, it can be extended to the experimental design of other magnetic alloys.

This study focused on the development of Fe–Co/kaolin catalyst by a wet impregnation method. Response surface methodology was used to study the influence of operating variables such as drying temperature, drying time, mass of support and stirring speed on the yield of the catalyst. The catalyst composite at best synthesis conditions was then calcined in an oven at varied temperature and time using 22 factorial design of experiment. The catalyst with optimum surface area was then utilized to grow carbon nanofiber (CNF) in a chemical vapour deposition (CVD) reactor. Both the catalyst and CNF were characterized using high-resolution scanning electron microscopy, high-resolution transmission electron microscopy, thermogravimetric analysis (TGA), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy. On the influence of operating variables on the yield of catalyst, the results showed that an optimum yield of 96.51% catalyst was obtained at the following operating conditions: drying time (10 h), drying temperature (110 °C), stirring speed (100 rpm) and mass of support (9 g). Statistical analysis revealed the existence of significant interactive effects of the variables on the yield of the catalyst. The HRSEM/XRD/BET/TGA analysis revealed that the particles are well dispersed on the support, with high surface area (376.5 m2/g) and thermally stable (330.88 °C). The influence of operating parameters on the yield of CNF was also investigated and the results revealed an optimum yield of 348% CNF at the following operating conditions: reaction temperature (600 °C), reaction time (40 min), argon flow rate (1416 mL/min) and acetylene/hydrogen flow rate (1416 mL/ min). It was found from statistical analysis that the reaction temperature and acetylene/hydrogen flow rates exerted significant effect on the CNF yield than the other factors. The contour and surface plots bi-factor interaction indicated functional relationship between the response and the experimental factors. The characterization results showed that the synthesized CNF is thermally stable, twisted and highly crystalline and contain surface functional groups. It can be inferred from the results of various analyses that the developed catalyst is suitable for CNF growth in a CVD reactor.