The purpose of this study is to review the available literature on the effectiveness of fibers in preventing early-age shrinkage cracking on cementitious concrete. The overview describes the widely used ASTM C1579 (Standard Test Method for Evaluating Plastic Shrinkage Cracking of Restrained Fiber Reinforced Concrete (Using a Steel Form Insert) for plastic shrinkage cracking. The past literature used crack length, width, or area to describe and quantify cracks on concrete specimens. To keep things simple, this review expresses the length, width or area as a percentage of the control specimen. Finally, the study establishes a relationship between fiber volume and aspect ratio on plastic shrinkage and compressive strength of concrete. It was concluded that fiber is sufficient enough to mitigate plastic shrinkage cracking. An increase in fiber volume and aspect ratio reduces the early-age cracking of concrete but harm its compressive strength.

Cellulose has experienced a renaissance as a precursor for carbon fibers (CFs). However, cellulose possesses intrinsic challenges as precursor substrate such as typically low carbon yield. This study examines the interplay of strategies to increase the carbonization yield of (ligno-) cellulosic fibers manufactured via a coagulation process. Using Design of Experiments, this article assesses the individual and combined effects of diammonium hydrogen phosphate (DAP), lignin, and CO2 activation on the carbonization yield and properties of cellulose-based carbon fibers. Synergistic effects are identified using the response surface methodology. This paper evidences that DAP and lignin could affect cellulose pyrolysis positively in terms of carbonization yield. Nevertheless, DAP and lignin do not have an additive effect on increasing the yield. In fact, combined DAP and lignin can affect negatively the carbonization yield within a certain composition range. Further, the thermogravimetric CO2 adsorption of the respective CFs was measured, showing relatively high values (ca. 2 mmol/g) at unsaturated pressure conditions. The CFs were microporous materials with potential applications in gas separation membranes and CO2 storage systems.

To improve the thermophysical properties of Al alloy for thermal management materials, the Cu-coated carbon fibers (CFs) were used as reinforcement to improve the thermal conductivity (TC) and the coefficient of thermal expansion (CTE) of Al-12Si. The CFs reinforced Al matrix (CFs/Al) composites with different CFs contents were prepared by stir casting. The effects of the CFs volume fraction and Cu coating on the microstructure, component, TC and CTE of CFs/Al composites were investigated by scanning electron microscopy with EDS, X-ray diffraction, thermal dilatometer and thermal dilatometer. The results show that the Cu coating can effectively improve the interface between CFs and the Al-12Si matrix, and the Cu coating becomes Al2Cu with Al matrix after stir casting. The CFs/Al composites have a relative density greater than 95% when the volume fraction of CFs is less than 8% because the CFs uniform dispersion without agglomeration in the matrix can be achieved by stir casting. The TC and CTE of CFs/Al composites are further improved with the increased CFs volume fraction, respectively. When the volume fraction of CFs is 8%, the CFs/Al composite has the best thermophysical properties; the TC is 169.25 W/mK, and the CTE is 15.28 × 10– 6/K. The excellent thermophysical properties of CFs and good interface bonding are the main reasons for improving the thermophysical properties of composites. The research is expected to improve the application of Al matrix composites in heat dissipation neighborhoods and provide certain theoretical foundations.

본 연구에서는 PVA(Poly Vinyl Alcohol)섬유와 GO(Graphene Oxide)를 혼입한 섬유보강 콘크리트(FRC)의 역학적 특성 을 평가하고자 하였다. GO와 PVA 섬유를 동시에 혼입한 FRC 각각의 재료를 단일로 사용하였을 때보다 기대효과가 다소 미흡 하였지만, 각 재료의 하이브리드화로 인장강도가 개선되면서 PVA 섬유 혼입률 0.1∼0.3%과 GO 혼입률 0.025%에서 우수한 효 과를 얻을 수 있었다. 특히 PVA 섬유는 0.3%로 혼합하였을 때 부작용을 최소화하면서 최대의 효과를 보였지만, 적절한 GO 배 합비를 조절할 필요가 있으며 FRC내 GO와 PVA 섬유의 최적배합을 구하기 위한 추가적인 연구가 필요할 것으로 사료된다.

현장에 적용하는 콘크리트 강도가 증가함에 따라 초고성능 콘크리트의 적용 분야가 넓어지고 있다. 초고성능 콘크리 트에는 강섬유를 일반적으로 사용하고 있지만, 이를 대체하기 위해 다양한 섬유를 연구에 적용하고 있다. 대표적으로 슈퍼섬유 라고 알려진 아라미드 섬유가 있다. 본 연구에서는 초고성능 콘크리트의 특성이 구조물 보수보강 및 내진보강에 적용하기에 적 합하다고 판단하여, 슈퍼섬유 중 하나인 파라아리미드 섬유와 조합한 복합섬유를 혼입한 초고성능 콘크리트를 보-기둥 접합부에 내진보강재로 활용하여 특성을 분석하였다. 초고성능 콘크리트의 내진보강 효과를 확인하였으며 내진상세를 적용한 실험체와 유사한 거동을 확인하였다. 초고성능 콘크리트의 높은 강도로 인해 기존 콘크리트가 파괴되는 양상이 나타나 초고성능 콘크리 트의 보수보강 효과를 모두 발휘하지 못하고 있어 추가 연구를 통해 최적의 보강단면을 설정한다면 내진보강재료로 활용할 수 있을 것으로 판단된다.

This paper investigates the effects of aspect ratio and volume fraction of hooked-end normal-strength steel fibers on the compressive and flexural properties of high-strength concrete with specified compressive strength of 60 MPa. Three types of hooked-end steel fibers with aspect ratios of 64, 67 and 80 were considered and three volume fractions of 0.25%, 0.50% and 0.75% for each steel fiber were respectively added into each high-strength concrete mixture. The test results indicated that the addition of normal-strength steel fibers is effective to improve compressive and flexural properties of high-strength concrete but fiber aspect ratio had little effect on the modulus of elasticity and compressive strength. As steel fiber content and aspect ratio increased, flexural beahvior of notched high-strength concrete beams was effectively improved.

With a strive to develop light-weight material for automotive and aerospace applications, aluminum-based hybrid nanocomposites (AHNCs) were manufactured utilizing the compocasting approach in this study. Chopped carbon fibers (CFs) are reinforced along with different weight fractions of nanoclay (1–5%) in the matrix of AA6026 forming AHNCs. The AHNCs specimens were examined by microstructural analysis, mechanical characterization, fatigue, and corrosion strength as per ASTM guidelines. Electroless plating method is adopted for coating CFs with copper to improve the wettability with matrix. SEM pictures of manufactured composites reveal thin inter-dendritic aluminum grains with precipitate particle of eutectic at intergranular junctions, as well as nanoclay particles that have precipitated in the matrix. Tensile strength (TS) rises with inclusion of nanoclay up to a maximum of 212.46 MPa for 3% nanoclay reinforcement, after which the TS is reduced due to non-homogeneity in distribution, agglomeration and de-bonding of nanoparticles. Similarly, micro-hardness increases with addition of 3% nanoclay after which it decreases. Higher energy absorption was achieved with 3% nanoclay reinforced hybrid and a significant improvement in flexural strength was obtained. With addition of both CFs and nanoclay, the fatigue strength of the hybrid composite tends to increase due to flexible CFs and high surface area nanoclays which strengthen the grain boundaries until 3% addition. Addition of nanoclay lowers the corrosion rate with nanoclays filling the crevices and voids in the matrix.

The evolvement in the microstructure and electrical properties of PAN-based carbon fibers during high-temperature carbonization were investigated. The study showed that as the heat treatment temperature increases, the change of carbon fiber resistivity around 1100 °C can be divided into two stages. In the first stage, the carbon content of the fiber increased rapidly, and small molecules such as nitrogen were gradually released to form a turbostratic of carbon crystal structure. The resistivity dropped rapidly from 3.19 × 10− 5 Ω·m to 2.12 × 10− 5 Ω·m. In the second stage, the carbon microcrystalline structure gradually became regular, and the electron movement area gradually became larger. At this time, the resistivity further decreases, from 2.12 × 10− 5 Ω·m to 1.59 × 10− 5 Ω·m. During carbonization, the tensile strength of carbon fiber first increased and then decreased. This is because the irregular and disordered graphite structure is formed first. As the temperature rose, the graphite layer spacing decreased and the grain thickness gradually increases. The modulus also gradually increased.

Thermal protection systems (TPS) are a group of materials that are indispensable for protecting spacecraft from the aerodynamic heating occurring during entry into an atmosphere. Among candidate materials for TPS, ceramic insulation materials are usually considered for reusable TPS. In this study, ceramic insulation materials, such as alumina enhanced thermal barrier (AETB), are fabricated via typical ceramic processing from ceramic fiber and additives. Mixtures of silica and alumina fibers are used as raw materials, with the addition of B4C to bind fibers together. Reaction-cured glass is also added on top of AETB to induce water-proof functionality or high emissivity. Some issues, such as the elimination of clumps in the AETB, and processing difficulties in the production of reusable surface insulation are reported as well.

The pitch-based activated carbon fibers (ACFs) were prepared from ethylene tar-derived pitches containing nickelocene (CNi) or nickel nitrate (NiN). The effects of different anions and contents of metal salts on the microstructure and surface chemical properties of fibers were investigated. The results revealed that Ni2+ from CNi mainly remained its pristine molecule in the organometal salt-derived pitch (OP-xCNi), while Ni2+ from NiN occurred complexation reaction with polycyclic aromatic hydrocarbons (PAHs) in the inorganic metal salt-derived pitch (IP-xNiN) due to the weaker binding ability between anions and Ni2+ of CNi than CNi. The XRD and SEM results confirmed that IP-3NiN-ACF contained Ni, NiO, Ni2O3 nanoparticles with different size distributions, while OP-3CNi-ACF only contained more uniformly distributed Ni nanoparticles with small size. Furthermore, OP-3.0CNi-ACF presented higher specific surface area of 1862 m2/ g and a pore volume of 1.69 cm3/ g than those of IP-3.0NiN-ACF due to the formation of pore structure during the in-situ catalytic activation of different metal nanoparticles. Therefore, this work further pointed out that the desired pore structure and surface chemistry of pitch-based ACFs could be obtained through regulating and controlling the interaction of anion species, metal cations and PAHs during the synthesis of pitch precursors.

To address the need for a suitable thermoplastic resin-based sizing agent for accommodating the increasing demands of carbon fiber-reinforced plastic, in this work, alcohol-soluble polyamide 6 (PA6) and silane were chemically combined in a certain ratio to improve the mechanical interface properties of the carbon fiber/PA6 composite, and the enhancement in the mechanical interface strength of the final composite according to the treatment time was confirmed. Carbon fiber surface properties were analyzed through ultrahigh-resolution field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy, and Fourier transform infrared spectrometry. The tensile strength of carbon fibers before and after hybrid sizing treatment and the mechanical interfacial shear strength of the final composite were analyzed using tensile and universal testing machines, respectively. After the hybrid sizing treatment, the introduction of the sizing agent to the carbon fiber surface was confirmed through FE-SEM, and a simultaneous increase in the surface roughness was observed. Moreover, the interfacial adhesion was confirmed to increase significantly, as compared to that of the desized carbon fiber. Therefore, this modified sizing agent treatment serves as an effective method for improving the mechanical interfacial adhesion between the carbon fiber and the PA6 matrix.

Glass wool, the primary material of insulation, is composed of glass fibers and is used to insulate the temperature of steam generators and pipes in nuclear power plants. Glass fiber is widely adopted as a substitute for asbestos classified as a carcinogen. The insulations used in nuclear power plants are classified as radioactive waste and most of the insulation is Very Low-Level Waste (VLLW). It is packaged in a 200 L drum the same as a Dry Active Waste (DAW). In the case of the insulations, it is packaged in a vinyl bag and then charged into the drum for securing additional safety because of the fine particle size of the fiberglass. A safety assessment of the disposal facility should be considered to dispose of radioactive waste. As a result of analyzing overseas Waste Acceptance Criteria (WAC), there is no case that has a separate limitation for glass fiber. Also, in order to confirm that glass fibers can be treated in the same manner as DAW, research related to the diffusion of glass fibers into the environment was conducted in this paper. It was confirmed that the glass fiber was precipitated due to the low flow velocity of groundwater in the Gyeongju radioactive waste repository and did not spread to the surrounding environment due to the effect of the engineering barrier. Therefore, the glass fiber has no special issue and can be treated in the same way as a DAW. In addition, it can be disposed of in the disposal facility by securing sufficient radiological safety as VLLW.

This study investigates the preparation of activated carbon fiber derived from waste cotton fabric for economical and ecofriendly recycling as well as its application to water purification. The activated carbon fiber was prepared by physical activation using steam and the adsorption property was then evaluated using methylene blue. When the activation temperature increased, the specific surface area and mesopore volume of the activated carbon fiber increased up to 2562 m2/ g and 0.214 cm3/ g, resulting in the increased adsorption of methylene blue. The results of the adsorption experiment for the activated carbon fiber were analyzed using the Langmuir and Freundlich equations. The Langmuir equation was more suitable than the Freundlich equation to explain the adsorption equilibrium. The maximum adsorption amount of methylene blue was 161.1–731.5 mg/g for fiber samples activated at temperatures ranging from 750 to 950 °C with sample labeled 750SA to 900SA according to the Langmuir equation. The kinetics of methylene blue adsorption by the activated carbon fiber were analyzed using non-linear pseudo-first-order and pseudo-second-order. Sample 750SA was suitable for the pseudo-first-order and 800SA, 850SA, and 900SA sample were suitable for the pseudo-second-order. Therefore, waste cotton fabric has the potential to be the precursor for activated carbon fiber with excellent adsorption properties.

This study assessed the changes in the fiber properties of virgin and recovered fibers from lab-scale and pilot-scale depolymerization reactors based on the thermal air oxidation-resistance characteristics. Lab-scale and pilot-scale depolymerization reactors had different depolymerization volumes. Results showed that the lab-scale and pilot-scale peak solvent temperatures were 185 °C and 151 °C, respectively. The lab-scale had highest solvent temperature rate increase because of the small depolymerization volume and the dominant role of the cavitation volume. The structural properties of the recovered and virgin fibers were intact even after the depolymerization and after the pretreatment and oxidation-resistance test. We observed 1.213%, 1.027% and 0.842% weight loss for the recovered (lab-scale), the recovered (pilot-scale) and virgin fibers because of the removal of impurities from the surface and chemisorbed gases. Further, we observed 0.8% mass loss of the recovered fibers (lab-scale) after the oxidative-onset temperature because of the “cavitation erosion effect” from the dominant of the cavitation bubbles. The “cavitation erosion effect” was subdued because of the increased depolymerization volume in the pilot-scale reactor. Therefore, negligible impact of the pilot-scale mechanochemical recycling process on the structure and surface characteristics of the fibers and the possibility of reusing the recovered fibers recycling process were characteristic. Representative functional groups were affected by the thermal oxidation process. We conducted HPLC, HT-XRD, TGA– DSC, XPS, SEM, and AFM analysis and provided an extensive discussion of the test thereof. This study highlighted how misleading and insufficient small-lab-scale results could be in developing viable CFRP depolymerization process.

The electrochemical capacitive properties of biomass-derived activated carbons are closely dependent on their microscopic structures. Here, activated carbon fibers (ACFs) were prepared from natural cattail fibers by carbonization and further chemical activation. The activation temperature affected on the microscopic structures and electrochemical properties of the activated carbon fibers. The results show that the optimum activation temperature is 800 °C. And the as-prepared ACF- 800 possesses high micropore specific surface area of 710.4 m2 g− 1 and micropore volume of 0.313 cm3 g− 1, respectively. For supercapacitor applications, the ACF-800 displays a high specific capacitance of 249 F g− 1 at a current density of 0.05 A g− 1, excellent rate performance and cycle stability in a three-electrode system. The excellent electrochemical performance indicated that the obtained activated carbon fibers could be a promising electrode material in supercapacitor.

To thoroughly analyze the mechanical properties and surface conditions of HF50S carbon fibers, the tensile properties, surface morphology, surface chemical element, surface energy, sizing agent properties, and Naval Ordnance Laboratory (NOL) ring of their composites were characterized. Furthermore, the aforementioned properties were exhaustively compared with those of T1000G carbon fibers. The results showed that the tensile strength, modulus, and elongation of the HF50S carbon fibers were 6638 MPa, 297 GPa, and 2.2%, respectively, thus demonstrating that the mechanical properties of the HF50S carbon fibers were on par with those of the T1000G carbon fibers, in addition, the coefficient of variation (Cv) indices of HF50S carbon fiber were below 3%, indicating good stability. The HF50S carbon fibers have a smooth surface without grooves, which is analogous to that of the T1000G carbon fibers prepared by the typical dry jet–wet spinning process. The main component of the sizing agent of the HF50S carbon fibers is an epoxy resin, which is also used for the preparation of epoxy matrix composites. Because the HF50S carbon fiber surface has greater O and N contents than the T1000G carbon fiber surface, the HF50S carbon fibers have more active functional groups and higher surface activity. The surface energy of the HF50S carbon fibers is 30.13 mJ/m2, which is higher than that of the T1000G carbon fibers (28.42 mJ/m2). Owing to the higher strength and surface activity of the HF50S carbon fibers than those of the T1000G carbon fibers, the strength and strength conversion of NOL ring based on the former are slightly higher than those of that prepared using the latter.