탄소섬유 강화 플라스틱 (Carbon fiber reinforced plastics, CFRP)은 고함량의 탄소섬유 (Carbon fiber, CF)와 고분자로 이루어진 복합재료로서, 뛰어난 기계적 성능으로 항공우주, 자동차, 토목 등 다 양한 산업 분야에서 사용되고 있다. 하지만 사용량 증가에 따른 폐기물의 환경문제와 추출한 재활용 탄소섬유 (Recycled carbon fiber, rCF)의 적용 가능 분야의 한계로 인해 재활용이 제한적인 실정이 다. 본 연구에서는 rCF와 CF 혼입 시멘트계 전자파 복합재를 제작하여 그 성능을 비교 분석하기 위 한 실험을 수행하였다. 구성재료는 시멘트, 잔골재, 고성능 감수제를 사용하였으며, 비교 분석을 위해 CF와 rCF를 각각 6 mm, 12 mm 길이를 0.1, 0.3, 0.5, 1.0 wt.% 함량으로 사용하였다. 전자파 복합 재의 흡수 성능 향상을 위해 각각 다른 함량의 다층 구조를 형성하였으며, 전자파 투과를 낮은 함량에 서 높은 함량 방향이 되도록 측정을 진행하였다. 전자파 차폐성능은 재령 28일 이후 네트워크 분석기 를 사용하여 자유 공간에서 측정하였으며, C-band (4~8 GHz)와 X-band (8~12 GHz) 주파수 영역 에서의 반사율과 투과율을 각각 측정하였다.

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 research, reduced graphene oxide/polypyrrole (rGO/PPy) particles were synthesized and used to measure the amount of dopamine (DA) electrochemically. The obtained rGO/PPy particle was characterized by Fourier Transform Infrared Spectrophotometer (FTIR), UV–Visible Spectrophotometer (UV–Vis), and X-Ray Diffraction Diffractometry (XRD). To investigate the DA sensor performance, cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used to acquire electrochemical measurements of the sensor. Current values of 1.65 and 5.9 mA were observed in the CV at 0.2 mM and 1.2 mM concentrations of target molecule, respectively. Under optimized conditions, the linear calibration plots were found to exhibit significant sensitivity in the linear range of 0.2 and 1.2 mM, with a corresponding detection limit of 0.061 μM for DA. The results obtained were similar to the sensor results of DA made using precious metals. This work was a demonstration of the feasibility of high-sensitivity electrochemical analysis with conductive carbon materials without the use of precious metals. It was also observed that the cost-effective rGO/PPy exhibited a very high potential for DA detection.

Energy storage for sustainable development and progress of power production industries is vitally important. The energy storage devices are under extensive research from last three decades to ensure the hand-on-hand coordination with power supply phenomenon and to reduce the energy loses in lines. The cost-effective materials are still highly demanding as an electrode material for energy storage devices. Biomass-derived carbon materials are best candidates due to their low cost, relatively high abundance, pollution-free nature. Here, we are reporting a facile two-step green approach to convert Himalayan horse chestnuts (HHCNs) into activated carbon materials. In first step, grinding and pyrolysis of the HHCNs were carried out, and then activation was performed using KOH to enhance the pore density and surface area. HHCNs-derived carbon was utilized as an electrode in electrical double-layer capacitors (EDLCs) with 1 M H2SO4 as an electrolyte. The macroporous structure along with hierarchical porous network acts as an efficient source of transportation of charges across the electrode and separator. Cyclic voltammetry test was taken from 10 to 100 mV/s current and within a range of 0–1 V applied potential; approximately rectangular CV shown mirror response towards current and shown typical EDLCs properties. The proximate analysis confirms the presence of heteroatoms like sulfur, oxygen, and nitrogen which act as carbon dopants. The wettability of HHCNs-derived carbon enhanced due to the various types of oxygen functionalities inherited from the lignin skeletal part. The nitrogen content is primarily responsible for the pseudo-capacitive behavior of HHCNs-codoped carbon. HHCNs-derived activated carbon materials has emerged as a promising electrode material for energy storage applications.

Activated carbon (AC) is used for filtering organic and radioactive particles, in liquid and ventilation systems, respectively. Spent ACs (SACs) are stored till decaying to clearance level before disposal, but some SACs are found to contain C-14, a radioactive isotopes 5,730 years halflife, at a concentration greater than clearance level concentration, 1 Bq/g. However, without waste acceptance criteria (WAC) regarding SACs, SACs are not delivered for disposal at current situation. Therefore, this paper aims to perform a preliminary disposal safety examination to provide fundamental data to establish WAC regarding SACs SACs are inorganic ash composed mostly of carbon (~88%) with few other elements (S, H, O, etc.). Some of these SACs produced from NPPs are found to contain C-14 at concentration up to very-low level waste (VLLW) criteria, and few up to low-level waste (LLW) criteria. As SACs are in form of bead or pellets, dispersion may become a concern, thus requiring conditioning to be indispersible, and considering VLL soils can be disposed by packaging into soft-bags, VLL SACs can also be disposed in the same way, provided SACs are dried to meet free water requirement. But, further analysis is required to evaluate radioactive inventory before disposal. Disposability of SACs is examined based on domestic WAC’s requirement on physical and chemical characteristics. Firstly, particulate regulation would be satisfied, as commonly used ACs in filters are in size greater than 0.3 mm, which is greater than regulated particle size of 0.2 mm and below. Secondly, chelating content regulation would be satisfied, as SACs do not contain chelating chemicals. Also, cellulose, which is known to produce chelating agent (ISA), would be degraded and removed as ACs are produced by pyrolysis at 1,000°C, while thermal degradation of cellulose occurs around 350~600°C. Thirdly, ignitability regulation would be satisfied because as per 40 CFR 261.21, ignitable material is defined with ignition point below 60°C, but SACs has ignition point above 350°C. Lastly, gas generation regulation would be satisfied, as SACs being inorganic, they would be targeted for biological degradation, which is one of the main mechanism of gas generation. Therefore, SACs would be suitable to be disposed at domestic repositories, provided they are securely packaged. Further analysis would be required before disposal to determine detailed radioactive inventories and chemical contents, which also would be used to produce fundamental data to establish WAC.

Refined structured tin dioxide gets the amount of attraction because of its low cost and stability. The C@SnO2 nanospheres with mesoporous structures were produced using the hard template method in this work. The C@SnO2 is primarily gained attributed to the dehydration condensation of C6H12O6 and the hydrolysis of SnCl4 ·5H2O. The morphology of the C@SnO2 was analyzed by physical characterization and the diameter of the obtained C@SnO2 was around 138 nm. When C@SnO2 was applied to lithium-ion batteries as anode material, it performed outstanding electrochemical properties, with a capacity of 735 and 539 mA h g− 1 maintained at 1000 and 2000 mA g− 1, respectively. Furthermore, it exhibits favorable discharge/ charge cycle stability. This is probably because of the more chemically redox active sites provided by C@SnO2 nanocomposites and it also allows fast ion diffusion and electron migration.

The study used the whole-life carbon assessment method to conduct a thorough carbon-neutral evaluation of a standard steel structure. To further assess carbon emissions, 11 design-changed models were evaluated, with changes made to the span between beams and columns. The results of the carbon emission assessment showed savings of approximately 13.1% by implementing the stage of the beyond life cycle. Additionally, the evaluation of carbon emissions through design changes revealed a difference of up to 42.2%. These findings confirmed that recycling and structural design changes can significantly reduce carbon emissions by up to 48.6%, making it an effective means of achieving carbon neutrality. It is therefore necessary to apply the stage of beyond life cycle and structural change to reduce carbon emissions.

The development of functional carbon materials using waste biomass as raw materials is one of the research hotspots of lithium-sulfur batteries in recent years. In this work, used a natural high-quality carbon source—coffee grounds, which contain more than 58% carbon and less than 1% ash. Honeycomb-like S and N dual-doped graded porous carbon (SNHPC) was successfully prepared by hydrothermal carbonization and chemical activation, and the amount of thiourea used in the activation process was investigated. The prepared SNHPC showed excellent electrochemical energy storage characteristics. For example, SNHPC-2 has a large pore volume (1.85 cm3·g− 1), a high mesoporous ratio (36.76%), and a synergistic effect (S, N interaction). As the cathode material of lithium-sulfur batteries, SNHPC-2/S (sulfur content is 71.61%) has the highest specific capacity. Its initial discharge-specific capacity at 0.2 C is 1106.7 mAh·g−1, and its discharge-specific capacity after 200 cycles is still as high as 636.5 mAh·g−1.

For the commercialization of hydrogen energy, a technology enabling safe storage and the transport of large amounts of hydrogen is needed. Porous materials are attracting attention as hydrogen storage material; however, their gravimetric hydrogen storage capacity (GHSC) at room temperature (RT) is insufficient for actual use. In an effort to overcome this limitation, we present a N-doped microporous carbon that contains large proportion of micropores with diameters below 1 nm and small amounts of N elements imparted by the nitrogen plasma treatment. The N-doped microporous carbon exhibits the highest total GHSC (1.59 wt%) at RT, and we compare the hydrogen storage capacities of our sample with those of metal alloys, showing their advantages and disadvantages as hydrogen storage materials.

Along with the development of the automobile industry, the materials and processing technology of parts have also developed. In particular, various materials have been developed and applied to automobile bumpers, which are directly related to crash safety. In particular, the application of composite materials is expanding for weight reduction. In this study, a new composite material made of a mixture of carbon fiber and aramid fiber was developed and the possibility of application to an automobile bumper was reviewed, and significant results were obtained.

In this study, soybean oil, which is used in a large variety of processed foods, is used as a carbon source. Soybean oil is successfully coated onto the surface of LiNi1/ 3Co1/3Mn1/3O2 (NCM) by a simple method. The physical and electrochemical properties of NCM/C hybrid materials are determined. As a result, a 5 nm thickness carbon coating layer is formed on the surface of the NCM, resulting in improved capability and cyclic performance in the battery. The NCM/C battery shows an initial discharge capacity of 159 mAh g−1 and 95% capacity retention after 100 cycles (a discharge capacity of 120 mAh g−1 and 94% retention are observed after 100 cycles for the NCM cathode).

Low thermal conductivity carbon fibers from polyacrylonitrile (PAN) are currently being explored as an alternative for traditional rayon-based carbon fibers with a thermal conductivity of 4 W/m K. Compared to multiple component electrospinning, this research demonstrated another feasible way to make low thermal conductivity carbon fibrous material by electrospinning PAN followed by carbonization and alkali activation. The effects of activation condition on microstructure, pore formation, and thermal conductivity of the resultant carbon nanofibrous material were investigated. The processing-structure-thermal conductivity relationship was revealed and mechanism of thermal conductivity reduction was discussed. The overall thermal conductivity of the prepared carbon nanofibrous material is a result of combined effects from factors of carbon structure and number of pores rather than volume of pores or specific surface area. The activated carbon nanofibrous materials showed thermal conductivity as low as 0.12 W/m K, which is a reduction of ~ 99% when compared to that of solid carbon film and a reduction of ~ 95% when compared to that of carbon nanofibrous material before activation.

본 연구에서는 “이온젤” 이라고 불리는 고분자 기반의 PVA(polyvinyl alcohol) 기반의 고체 전 해질에 이온성 액체 BMIMBF4 (1-buthyl-3-methylimidazolium tetrafluoroborate)를 첨가하여 제조한 전 고체 전해질과 활성탄소와 금속유기골격체 복합재료 기반의 전극 재료를 이용하여 슈퍼커패시터를 제작 하였으며, 유기골격체의 유 무에 따른 전기화학적 특성을 분석하여 보았다. 슈퍼커패시터의 전기화학적 특 성은 순환전압전류법(CV), 전기화학적 임피던스 분광법(EIS) 및 전정류 충·방전법(GCD)을 통하여 비교 및 분석하여 보았다. 그 결과로, 금속유기골격체가 함유되지 않은 슈퍼커패시터의 전기용량값은 380 F/g 으로 확인 할 수 있었고, 이 값은 금속유기골격체를 첨가하였을 때 340 F/g로 감소하는 현상을 확인할 수 있었 다. 이러한 결과로 1 wt%의 금속유기골격체의 함유량은 전기화학적 특성 감소에 영향을 주는 것으로 사료 되며 이러한 결과를 바탕으로 금속유기골격체의 첨가량을 최적화 할 필요가 있다고 판단된다

Spherical Li3V2(PO4)3 (LVP) and carbon-coated LVP with a monoclinic phase for the cathode materials are synthesized by a hydrothermal method using N2H4 as the reducing agent and saccharose as the carbon source. The results show that single phase monoclinic LVP without impurity phases such as LiV(P2O7), Li(VO)(PO4) and Li3(PO4) can be obtained after calcination at 800 oC for 4 h. SEM and TEM images show that the particle sizes are 0.5~2 μm and the thickness of the amorphous carbon layer is approximately 3~4 nm. CV curves for the test cell are recorded in the potential ranges of 3.0~4.3 V and 3.0~4.8 V at a scan rate of 0.01 mV s–1 and at room temperature. At potentials between 3.0 and 4.8 V, the third Li+ ions from the carbon-coated LVP can be completely extracted, at voltages close to 4.51 V. The carbon-coated LVP exhibits an initial specific discharge capacity of 118 mAh g–1 in the voltage region of 3.0 to 4.3 V at a current rate of 0.2 C. The results indicate that the reducing agent and carbon source can affect the crystal structure and electrochemical properties of the cathode materials.

본 연구에서는 탄소나노튜브/화이버/폴리머 복합소재 구조에 대한 재료 물성 및 강성 추정을 다룬다. 수정된 Halpin-Tsai 모델을 적용한 멀티 스케일 해석은 탄소나노튜브의 함유량 비율, CNT 두께-길이 비율, 화이버 부피 함유량, 그리고 화이버 보강각도 변화에 따라서 수행되었다. 본 연구에서 제시한 멀티-스케일 접근방법은 기존 모델을 적용하여 얻은 결과와 비교하여 검증하였다. 매개변수 해석을 통하여 CNT의 적절한 함유량은 적층된 CNTFPC 구조의 구조성능의 향상시킬 수 있는 중요한 특성을 규명하였다.

This research is conducted to create a functional hydrogel ophthalmic lens containing nanoparticles. Carbon nanoparticles and PEGMEMA are used as additives for the basic combination of HEMA, MA, and MMA, and the materials are copolymerized with EGDMA as the cross-linking agent and AIBN as the thermal initiator. The hydrogel lens is produced using a cast-mold method, and the materials are thermally polymerized at 100 oC for an hour. The polymerized lens sample is hydrated in a 0.9% saline solution for 24 hours before the optical and physical characteristics of the lens are measured. The refractive index, water content, contact angle, light transmittance, and tensile strength are measured to evaluate the physical and optical characteristics of the hydrogel lens. The refractive index, water content, contact angle, UV-B light transmittance, UVA light transmittance, visible light transmittance, tensile strength and breaking strength of the hydrogel lens polymer are 1.4019~1.4281, 43.05~51.18 %, 31.95~68.61o, 21.69~58.11 %, 35.59~84.26 %, 45.85~88.06 %, 0.1075~0.1649 kgf and 0.1520~0.2250 kgf, respectively. The results demonstrate an increase in refractive index, tensile strength and breaking strength and a decrease in contact angle and light transmittance. Furthermore, the visible light transmissibility is significantly increased at PEG 10 %. It is clear that this material can be used for high-performance ophthalmic lenses with wettability, ultraviolet ray blocking effect, and tensile strength.

한국의 도시산림을 대표하는 남산에 대표군락인 소나무 군락의 물질생산과 탄소분포의 특성을 밝히고자 2009년부 터 2017년까지 현존량, 순생산량, 식물체 유기탄소 분포량, 낙엽생산량, 낙엽의 유기탄소량, 임상낙엽량, 임상낙엽의 유기탄소량 그리고 토양의 깊이별 유기탄소 축적량을 조사 하였다. 교목층의 현존량은 측정한 흉고직경을 상대생장식 에 대입하여 매년 산출하였다. 2009년부터 2017년까지 교 목층의 현존량은 각각 153.96, 160.05, 160.55, 166.46, 170.21, 167.68, 174.25, 180.71 그리고 184.65 ton/ha 이었 다. 순생산량은 2009년부터 2016년까지 각각 7.01, 4.17, 2.88, 5.52, 4.68, 3.53, 2.62 그리고 6.74 ton/ha이었다. 식물 체의 유기탄소 분포량은 2009년부터 2017년까지 각각 69.28 72.02, 72.25, 74.91, 76.6, 75.45, 78.41, 81.32 그리 고 83.1ton/ha이었다. 낙엽생산량은 2009넌부터 2017년까 지 각각 7.23, 5.95, 2.58, 5.84, 6.26, 1.93, 1.43, 5.17그리고 4.89 ton/ha이었다. 낙엽생산을 통해 임상으로 유입되는 낙 엽의 유기탄소량은 2009년부터 2017년까지 각각 0.26, 0.21, 0.09, 0.21 0.23, 0.07, 0.05, 0.19 그리고 0.18 ton C/ha 이었다. 임상낙엽량은 2010년부터 2013년, 2016년 그리고 2017년에 각각 9.21, 8.84, 10.01, 9.34, 6.72 그리고 9.78 ton/ha이었다. 임상낙엽의 유기탄소량은 2010년부터 2013 년, 2016년 그리고 2017년에 각각 4.14, 3.98, 4.5, 4.2, 3.02 그리고 4.4 ton C/ha이었다. 토양의 깊이별 유기탄소 축적 량은 2009년부터 2012년, 2014년, 2016년 그리고 2017년 에 10cm, 20cm, 30cm, 40cm 그리고 50cm 깊이에서 각각 평균 37.60, 37.29, 36.42, 31.42 그리고 31.12 ton C/ha이었 다. 2014년 식물체의 탄소분포량이 가장 낮았는데, 이는 교목층 줄기의 현존량 증가율이 가장 적었기 때문이다. 또한, 2015년 순일차생산량이 다른 해보다 낮았는데, 이는 생육 기인 봄철(3~5월) 강수량이 평년보다 약 100mm 적었기 때문으로 해석된다.