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.

In this research, synergetic and separate influence of nano-carbon black (C.Bn) and SiC on the microstructure and flexural strength of ZrB2 were investigated. So, ZrB2 and ZrB2- 30vol%-based composites containing 10 and 15 vol% C.Bn as well as ZrB2- 15 vol% SiC were fabricated via spark plasma sintering at 1850 °C for soaking time of 8 min under the applied pressure of 35 MPa. Relative density was measured by Archimedes method. Microstructural evaluation was carried out by applying the field emission electron microscopy (FESEM), and flexural strength was measured by three-point bending test. It was found the relative density improves in the presence of C.Bn and SiC especially in synergetic state so that the full densification was gained in Z30Si10C.Bn and Z30Si15C.Bn composites through their reactions with impurities at 1850 °C. In the monolithic ZrB2 system, the C.Bn addition improves the flexural strength slightly to 300 MPa and 315 MPa from 290 MPa. However, co-doped 10 vol% C.Bn with 30 vol% SiC resulted to achieve maximum flexural strength of 486 MPa in comparison with individually applying each of them (395 MPa for Z30Si and 300 MPa for Z10 C.Bn).

In this study, we successfully grafted chitosan (CS) onto multi-walled carbon nanotubes (MWCNTs) to enhance their properties and potential applications in the biomedical field. FTIR spectroscopy confirmed the successful covalent bonding of CS onto MWCNTs, indicated by the new absorption peak of the amide bond (–CONH–). Thermal analysis showed that the modified MWCNTs (MWCNT-CS) had significant weight loss around 260 °C, suggesting the decomposition of hydroxypropyl chitosan, and confirming its presence in the nanocomposite. SEM images revealed that CS grafting improved the dispersibility of MWCNTs, a property crucial for their use as nanofillers in polymers. Moreover, the micro-tensile bond strength of dentin surface increased with increasing MWCNT-CS concentrations, indicating the potential of MWCNT-CS as a pretreatment for dentin bonding. After simulated aging, the bond strength remained significantly higher for MWCNT-CS groups compared to those without pretreatment. In biocompatibility assessment using the MTT assay, MWCNT-CS showed higher cell viability than MWCNT, suggesting improved biocompatibility after CS modification. The results of this study suggest that CS-modified MWCNTs could be promising materials for applications in dentin bonding, dentin mineralization, bone scaffolding, implants, and drug delivery systems.

Flexible supercapacitors (FS) are ideal as power backups for upcoming stretchable electronics due to their high power density and good mechanical compliance. However, lacking technology for FS mass manufacturing is still a significant obstacle. The present study describes a novel method for preparing FS based on reduced graphene oxide (RGO) using the N+ plasma technique, in which N+ reduces graphene oxide on the surface of a cotton/polyester substrate. The effect of aloe vera (AV) as a natural reducing & capping agent and carbon nanotubes (CNT) as nanoconductors on the electrochemical performance of the electrodes is studied. FESEM and XPS were employed to investigate the electrodes' structural and chemical composition of electrodes. The galvanostatic charge–discharge curves of electrodes revealed the enhancement of the electrochemical activity of the as-prepared electrode upon additions of AV and CNT. The areal capacitance of the RGO, RGO/AV, and RGO/ AV/CNT supercapacitors at 5 mV/s was 511, 1244.5, and 1879 mF/cm2, respectively. The RGO electrode showed capacitive retention of 80.9% after 2000 cycles enhanced to 89.7% and 92% for RGO/AV and RGO/AV/CNT electrodes, respectively. The equivalent series resistance of the RGO electrode was 126.28 Ω, decreased to 56.62 and 40.06 Ω for RGO/AV and RGO/ AV/CNT electrodes, respectively.

Sulfur and nitrogen co-doped carbon dots (NSCDs) were quickly synthesized by the microwave-assisted method from triammonium citrate and thiourea. NSCDs showed a quantum yield of 11.5% with excitation and emission bands at 355 and 432 nm, respectively. Also, a fluorescence quenching was observed in the presence of Pb(II) ions, and the as-synthesized CDs were used as a sensitive probe for detecting Pb(II) in water and food samples. The results showed the optimal conditions for Pb(II) determination were CDs concentration of 0.02 mg mL− 1 at pH 6.0–7.0 and an incubation time of 20 min. The relative fluorescence intensity of NSCDs was proportional to Pb(II) concentrations in the range of 0.029–2.40 and 2.40–14.4 μmol L− 1 with a correlation coefficient (R2) of 0.998 and 0.955, respectively, and a detection limit of 9.2 × 10– 3 μmol L− 1. Responses were highly repeatable, with a standard deviation below 3.5%. The suggested method demonstrates the potential of a green, fast, and low-cost approach for Pb(II) determination in water, tea, and rice samples with satisfying results.

Nitrogen and phosphorous dual-doped carbon nanotubes (N,P/CNT) have been grown in a single-step direct synthesis process by CVD method using iron-loaded mesoporous SBA-15 support, as an electrode material for the energy storage device. For comparison, pristine nanotubes, nitrogen and phosphorous individually doped nanotubes were also prepared. The basic characterization studies clarify the formation of nanotubes and the elemental mapping tells about the presence of the dopant. Under three-electrode investigations, N,P/CNT produced a maximum specific capacitance of about 358.2 F/g at 0.5 A/g current density. The electrochemical performance of N,P/CNT was further extended by fabricating as a symmetric supercapacitor device, which delivers 108.6 F/g of specific capacitance for 0.5 A/g with 15 Wh/kg energy density and 250 W/kg power density. The observed energy efficiency of the device was 92.3%. The capacitance retention and coulombic efficiency were 96.2% and 90.6%, respectively, calculated over 5000 charge–discharge cycles.

This study presents the synthesis, characterization, and utilization of marine macroalgae-derived bio-carbon catalysts (BC and KOH-AC) for the efficient conversion of waste cooking oil (WCO) into biodiesel. The biochar (BC) was produced through slow pyrolysis of macroalgal biomass, which was subsequently activated with potassium hydroxide (KOH) to produce a KOH-modified activated carbon (KOH-AC) catalyst. Advanced characterization techniques, including SEM, EDX, XRD, FTIR, and TGA, were used to examine the physicochemical characteristics of the catalysts. The synthesized catalysts were utilized to produce biodiesel from WCO, and the results revealed that the highest biodiesel yields, 98.96%, and 47.54%, were obtained using KOH-AC and BC catalysts, respectively, under optimal reaction conditions of 66 °C temperature, 12.3 M/O molar ratio, 130 min time, and 3.08 wt.% catalyst loading via RSM optimization. The kinetic and thermodynamic parameters, such as k, Ea, ΔH, ΔS, and ΔG, were determined to be 0.0346 min− 1, 43.31 kJ mol− 1, 38.98 kJ mol− 1, − 158.38 J K− 1 mol− 1, and 92.58 kJ mol− 1, respectively. The KOH-AC catalyst was recycled up to five times, with a significant biodiesel yield of 80.37%. The fuel properties of the biodiesel met ASTM (D6751) specifications, ensuring that it has excellent fuel characteristics and can be used as an alternative fuel.

Proton exchange membrane fuel cells (PEMFCs) are an auspicious energy conversion technology with the potential to address rising energy demands while reducing greenhouse gas emissions. The stack’s performance, durability, and economy scale are greatly influenced by the materials used for the PEMFC, viz., the membrane electrocatalyst assembly (MEA) and bipolar flow plates (BPPs). Despite extensive study, carbon-based materials have outstanding physicochemical, electrical, and structural attributes crucial to stack performance, making them an excellent choice for PEMFC manufacturers. Carbon materials substantially impact the cost, performance, and durability of PEMFCs since they are prevalently sought for and widely employed in the construction of BPPs and gas diffusion layers (GDLs)) and in electrocatalysts as a support material. Consequently, it is essential to assemble a review that centers on utilizing such material potential, focusing on its research development, applications, problems, and future possibilities. The prime focus of this assessment is to offer a clear understanding of the potential roles of carbon and its allotropes in PEMFC applications. Consequently, this article comprehensively evaluates the applicability, functionality, recent advancements, and ambiguous concerns associated with carbonbased materials in PEMFCs.

The need for high-performance environmental remediation has increased due to the environment’s ongoing degradation in the form of significant growth in industrialization and urbanization. Therefore, the toxic heavy metals can easily enter into environmental as well as foods and thus the search of clean water for drinking, household and irrigation purposes is of crucial importance. To meet this challenge, microelectrodes are flexible, low-cost and easier for fabrication has become the strong role in the detection of heavy metals with high sensitivity towards higher adsorption of heavy metals from contaminated water. To improve the sensitivity of the microelectrodes, carbon-based microelectrodes decorated with nanomaterials have been explored for the detection of metal ions thereby their presence in trace levels can be estimated. The aim of the present review is to summarize the recent developments in carbon-based microelectrodes for the electrochemical determination of heavy metals. It is followed by the various nanomaterials decorated on the carbon microelectrodes for detection of heavy metals was systematically discussed. Finally, the application and the future perspectives in the development of smart electrochemical sensing is provided. This short review will provide the useful information for the recent development in microelectrodes and also guide the pathway for the detection of heavy metals.

Tomatoes in greenhouse are a widely cultivated horticultural crop worldwide, accounting for high production and production value. When greenhouse ventilation is minimized during low temperature periods, CO2 enrichment is often used to increase tomato photosynthetic rate and yield. Plant-induced electrical signal (PIES) can be used as a technology to monitor changes in the biological response of crops due to environmental changes by using the principle of measuring the resistance value, or impedance, within the crop. This study was conducted to investigate the relationship between tomato growth data, vital response, and PIES resulting from CO2 enrichment in greenhouse tomatoes. The growth of tomato treated with CO2 enrichment in the morning was significantly better in all items except stem diameter compared to the control, and PIES values were also higher. The growth of tomato continuously applied with CO2 was better in the treatment groups than control, and there was no significant difference in chlorophyll fluorescence and photosynthesis. However, PIES and SPAD values were higher in the CO2 treatment group than control. CO2 enrichment have a direct relationship with PIES, growth increased, and transpiration increased due to the increased leaf area, resulting in increased water absorption, which appears to be reflected in PIES, which measures vascular impedance. Through this, this study suggests that PIES can be used to monitor crops due to environmental changes, and that PIES is a useful method for non-destructively and continuously monitoring changes of crops.

In this study, we synthesized pH-controlled resorcinol-formaldehyde (RF) gels through the polymerization of two starting materials: resorcinol and formaldehyde. The prepared RF gels were dried using an acetone substitution method, and they were subsequently carbonized under nitrogen atmosphere to obtain carbon xerogels (CX_Y) prepared at different pH (Y). The carbon xerogels were utilized as active materials for coin-type organic supercapacitor electrodes to investigate the influence of pH on the electrochemical properties of the carbon xerogels. The carbon xerogels prepared at lower pH (CX_9.5 and CX_10) exhibited sufficient particle growth, with a three-dimensional network of particles during the RF gel formation, resulting in the development of abundant mesopores. Conversely, the carbon xerogels prepared at higher pH (CX_11 and CX_12) retained densely packed structures of small particles, leading to pore collapse and low specific surface areas. Consequently, CX_9.5 and CX_10 showed high specific surface areas, and provided ample adsorption sites for the formation of electric double layers with electrolyte ions. Moreover, the three-dimensional particle network in CX_9.5 and CX_10 significantly enhanced electrical conductivity. The presence of well-developed mesopores in these materials further facilitated the effective transport of electrolyte ions, contributing to their superior performance as organic supercapacitor electrodes. This study confirmed that pH-controlled carbon xerogels are one of the promising active materials for organic supercapacitor electrodes. Furthermore, we concluded that pH during RF gel formation is a crucial factor determining the electrode performance of the carbon xerogels, highlighting the need for precise pH control to obtain high-performance carbon xerogel electrodes.

This study was aimed to determine the changes in CO2 concentration according to the temperatures of daytime and nighttime in the CO2 supplemental greenhouse, and to compare calculated supplementary CO2 concentration during winter and spring cultivation seasons. CO2 concentrations in experimental greenhouses were analyzed by selecting representative days with different average temperatures due to differences in integrated solar radiation at the growth stage of leaf area index (LAI) 2.0 during the winter season of 2022 and 2023 years. The CO2 concentration was 459, 299, 275, and 239 μmol·mol-1, respectively at 1, 2, 3, and 4 p.m. after the CO2 supplementary time (10:00-13:00) under the higher temperature (HT, > 18°C daytime temp. avg. 31.7, 26.8, 23.8, and 22.4°C, respectively), while it was 500, 368, 366, 364 μmol·mol-1, respectively under the lower temperature (LT, < 18°C daytime temp. avg. 22.0, 18.9, 15.0, and 13.7°C, respectively), indicating the CO2 reduction was significantly higher in the HT than that of LT. During the nighttime, the concentration of CO2 gradually increased from 6 p.m. (346 μmol·mol-1) to 3 a.m. (454 μmol·mol-1) in the HT with a rate of 11 μmol·mol-1 per hour (240 tomatoes, leaf area 330m2), while the increase was very lesser under the LT. During the spring season, the CO2 concentration measured just before the start of CO2 fertilization (7:30 a.m.) in the CO2 enrichment greenhouse was 3-4 times higher in the HT (>15°C nighttime temperature avg.) than that of LT (< 15°C nighttime temperature avg.), and the calculated amount of CO2 fertilization on the day was also lower in HT. All the integrated results indicate that CO2 concentrations during the nighttime varies depending on the temperature, and the increased CO2 is a major source of CO2 for photosynthesis after sunrise, and it is necessary to develop a model formula for CO2 supplement considering the nighttime CO2 concentration.

Transition metal chalcogenides are promising cathode materials for next-generation battery systems, particularly sodium-ion batteries. Ni3Co6S8-pitch-derived carbon composite microspheres with a yolk-shell structure (Ni3Co6S8@C-YS) were synthesized through a three-step process: spray pyrolysis, pitch coating, and post-heat treatment process. Ni3Co6S8@C-YS exhibited an impressive reversible capacity of 525.2 mA h g-1 at a current density of 0.5 A g-1 over 50 cycles when employed as an anode material for sodium-ion batteries. However, Ni3Co6S8 yolk shell nanopowder (Ni3Co6S8-YS) without pitch-derived carbon demonstrated a continuous decrease in capacity during charging and discharging. The superior sodium-ion storage properties of Ni3Co6S8@C-YS were attributed to the pitchderived carbon, which effectively adjusted the size and distribution of nanocrystals. The carbon-coated yolk-shell microspheres proposed here hold potential for various metal chalcogenide compounds and can be applied to various fields, including the energy storage field.

가스 분리 방법 중에서도, 멤브레인을 이용한 CO2 포집 및 분리는 지속적으로 개발되고 있는 꾸준히 성장하는 분 야이다. 이온성 액체(IL) 기반 복합 막은 CO2를 분리하는 데 있어 우수한 성능값을 보여준다. 유사하게, 다양한 공중합체/IL 복합막 또한 향상된 성능을 보여준다. 이러한 공중합체/IL 복합만에 산화그래핀과 같은 필러를 첨가하면 IL과 유기 필러 사 이에서 발생하는 강한 상호작용으로 인해 필러의 효과가 더욱 향상되며, 이는 결과적으로 CO2의 친화도, 선택도 및 흡착과 같은 요소를 향상시킨다. 금속-유기 구조체(MOF)를 사용하는 공중합체/IL 복합 막은 향상된 CO2 투과도를 보여주었다. 이 총설에서는 이온성 액체와 공중합체복합막의 다양한 조합에 따른 이산화탄소분리성능에 대한 상관관계를 논의한다.

이 연구는 코르크보드를 보강하여 건축부재 및 놀이기구의 안전부재 등으로 폭넓게 활용할 것을 목적으로 코르크보드의 중층에 금속, 유리섬유, 탄소섬유를 삽입하여 보강한 3종의 코르크복합보드를 제조하였고, 코르크복합보드의 수분흡수에 따른 치수안정성 및 접착층 박리성능을 조사하였다. 코르크복합보드의 흡수율은 0.37% - 0.45%의 범위에 있었고, 코르크보드에 비해 0.61배 - 0.74배의 낮은 값을 나타내었다. 코르크복합보드의 두께팽창률은 0.92% - 1.58%의 범위에 있었고, 코르크보드 보다 1.4 - 2.4배의 높은 값을 나타내었다. 그러나 이 값들은 일반 목질보드보다 현저히 낮았고, KS규격의 12%이하를 하회하는 것이 확인되었다. 코르크복합보드의 준내수 및 내수침지박리시험후의 접착층박리율은 0%로 전혀 접착층의 박리가 일어나지 않아 우수한 내수성을 나타내었고, 흡수율과 흡수두께팽창률은 상온침지에 비해 다소 증가하였으나, 목질보드에 관한 KS규격을 하회하는 우수한 치수안정성을 나타내는 것이 확인되었다.

본 연구는 난대상록수종인 종가시나무에 대한 수간곡선식의 도출과 재적표의 작성 및 탄소배출계수를 이용하여 탄소저장, 흡수량을 추정하고자 수행하였다. 분석에 사용된 공시목은 전남, 경남, 제주 등에서 수집된 468본이며, 수간형태를 도출하기 위하여 적용한 수간곡선 모형은 Kozak 모델이다. 이 모델의 적합도는 0.9452, 편의는 0.0807, 추정치 표준오차의 백분율은 1.7145, 평균절대편차는 1.2655로 각각 나타났다. 종가시나무의 개체목 재적은 Kozak 수간곡선 모델에 Smalian 재적식을 적용시켜 산출하였으며, 수고와 흉고직경급별로 재적표를 작성하였다. 그리고 붉가시나무 재적표와 이번에 만든 종가시나무 재적표를 서로 비교한 결과(t-test), 통계적으로 두 집단 간에 차이가 없는 것으로 나타났다. 따라서 이들 재적표는 두 수종 중 하나만 이용하거나, 둘을 하나로 통합하여도 문제가 없을 것으로 판단된다. 한편 종가시나무림의 탄소저장 및 흡수량은 산림바이오소재연 구소 시험림의 조사구를 대상으로 하였다. 이들 조사구를 대상으로 탄소저장 및 흡수량을 계산한 결과, 생육상태가 양호한 시험구(A)에서 탄소저장량 은 93.17 C ton/ha, 그리고 탄소흡수량은 13.14 CO2 ton/ha/yr 인 것으로 나타났다. 반면에 생육이 저조한 시험구(B)의 탄소 저장 및 흡수량은 양호한 시험구보다 약 1/3 정도 낮게 나타났다.

기후변화 위기에 대응하기 위하여 대한민국은 2030년까지 신재생연료 혼합비율(Renewable Fuel Standard, RFS)을 3.5%에서 8%까지 상향하기로 결정하였다. 국내에서 제조되는 신재생연료의 원료가 되는 바이오매스의 60%이상이 해외에서 수입하는 실정이며, 2030 탄소중립 및 RE100과 같은 바이오연료 사용증가 정책의 확대로 인하여 국내에서 제조되어 활용가능한 바이오매스의 확보가 절실하게 필요하다. 곤충은 높은 비율의 단백질과 지질을 체내에 저장하는 특징을 가지고 있으며, 곤충의 대량사육을 통하여 지질의 대량생산이 가능할 것으로 판단된다. 본 연구에서는 곤충의 대량사육환경에서 제조되는 지질을 원료로 하여 기후변화에 대응할 수 있는 바이오연료로의 전환 제조가능성을 확인하고자 하였으며, 이를 위하여 촉매공정을 통하여 디젤과 혼합하여 사용할 수 있는 수첨바이오디젤을 제조하여 그 특성을 분석하였다. 그 결과 곤충지질을 활용하여 수첨바이오디 젤로 전환가능함을 확인하였다.