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.
아미노글리코사이드계 항생제(Aminoglycosides, AGs) 는 그람음성균과 양성균에 광범위하게 작용하는 동물용 의약품으로, 최근 배양육에 사용된다고 알려져 있어, 안 전성 관리를 위한 분석법 마련이 반드시 필요하다. AGs 는 고극성 화합물로 성분 간의 분리를 위해 이온쌍 시 약(ion-pairing reagent, IPR)을 사용하고 있으나 IPR을 이동상에 첨가하는 기존 분석방법의 경우 용매가 흐르 는 동안 질량분석기로 주입되는 IPR로 인해 기기적인 문 제가 발생할 가능성이 높아, IPR를 바이알에 직접 첨가 하는 분석방법을 검토하였다. 본 연구에서 10종 AGs 성 분에 대한 분석방법을 확인하고 유효성을 검증하였다. 검출한계와 정량한계는 각각 0.0001-0.0038 mg/kg 와 0.004-0.011 mg/kg의 범위로 나타났으며, 0.01-0.5 mg/ kg 범위 내의 직선성(R2)은 0.99 이상이었다. AGs의 시 료 회수율을 확인하고자 소고기와 세포배양배지(cell culture medium) 매질에서 회수율과 상대표준편차로 나 타낸 정밀도를 확인한 결과 각각 70.7-120.6% 및 0.2 to 24.7%로 나타났다. 기존의 이동상에 IP 첨가 방법과 비 교하였을 때 유사한 수준으로 양호하였다. 검증된 AGs 분석법은 국내 유통되는 닭고기, 소고기, 돼지고기 15품 목과 배양육 배지 첨가제 6품목에 적용해보았다. 그 결 과 국내 유통되는 육류 15품목 모두 AGs 성분이 검출 되지 않았으나, 세포배양배지에서 streptomycin은 695.85- 1152.71 mg/kg, dehydrostreptomyci은 6.35-11.11 mg/kg 로 검출되었다. 따라서 IRR을 바이알에 직접 첨가하는 LC-MS/MS 방식은 육류, 세포배양배지, 배지첨가제 중 AGs 분석 및 안전성 평가를 위한 기초자료로 활용될 것 으로 기대된다.
막 축전식 탈염 공정(membrane capacitive deionization, MCDI)은 이온교환막을 다공성 전극과 함께 사용하여 탈 염 효율을 향상시킬 수 있는 CDI 공정의 변형이다. 이온교환막은 MCDI의 성능에 큰 영향을 미치는 핵심 구성요소이다. 본 연구에서는 MCDI의 탈염 효율을 크게 향상시킬 수 있는 이온교환막의 최적 제조 인자를 도출하고자 하였다. 이를 위해 PE 다공성 필름의 세공에 단량체를 충진하고 in-situ 광중합을 진행하여 세공충진 이온교환막(pore-filled ion-exchange membranes, PFIEMs)을 제조하였다. 실험 결과, 제조된 PFIEMs은 다양한 탈염 및 에너지 변환 공정에 적용할 수 있는 수준의 우 수한 전기화학적 특성을 나타내었다. 또한, MCDI 성능과 막 특성 인자와의 상관성 분석을 통해 막의 가교도를 제어하여 막 의 전기적 저항이 충분히 낮은 범위에서 이온 선택 투과성을 최대화하는 것이 MCDI의 성능 향상을 위해 가장 바람직한 막 제조 조건이라는 결론을 얻었다.
최근 우리는 Hg2+에 대한 높은 선택성을 가지며 Hg2+와 결합하여 밝은 녹색 형광을 보이는 tetraphenylethylene-bis(thiophen-2-ylmethyl)amine (TPE-BTA)의 착화합물(TPE-BTA-2Hg2+)의 구조를 밝혀내기 위해 시 간 의존적(time-dependent, TD) 밀도 함수 이론(DFT)을 이용하였다. 그러나 우리는 이 과정 속에서 Hg2+ 이온에 대한 모든 전자(all electron, AE) basis set인 x2c-TZVPPall만이 실험 스펙트럼에 가까운 흡수 및 형광 스펙트럼을 성공적으 로 재현한다는 것을 발견했다. 많이 알려져 있는 effective core potential (ECP) 기반인 LANL2DZ는 형광스펙트럼 계산 과 관련된 들뜬 상태의 구조 최적화 계산을 모두 실패했으며 또한, LANL2DZ는 첫 번째 들뜬 상태의 최적화 과정에서 너무 작은 형광 에너지를 제공했다. 이때 LANL2DZ는 리간드와 Hg2+ 사이의 거리가 증가함에 따라 빠르게 감소하는 HOMO-LUMO gap을 제공하는 반면, x2c-TZVPPall은 점진적으로 감소하는 안정적인 HOMO-LUMO gap을 보여줬다. 우리는 적어도 Hg2+ 이온을 포함하는 착화합물 시스템에서 ECP에서 발생하는 기하학적 문제들을 피하기 위해서는 모 든 전자 기본 세트를 사용하거나 새로운 ECP를 만들어야 된다고 조심스럽게 제안한다.
Small-film-type ion sensors are garnering considerable interest in the fields of wearable healthcare and home-based monitoring systems. The performance of these sensors primarily relies on electrode capacitance, often employing nanocomposite materials composed of nano- and sub-micrometer particles. Traditional techniques for enhancing capacitance involve the creation of nanoparticles on film electrodes, which require cost-intensive and complex chemical synthesis processes, followed by additional coating optimization. In this study, we introduce a simple one-step electrochemical method for fabricating gold nanoparticles on a carbon nanotube (Au NP–CNT) electrode surface through cyclic voltammetry deposition. Furthermore, we assess the improvement in capacitance by distinguishing between the electrical double-layer capacitance and diffusion-controlled capacitance, thereby clarifying the principles underpinning the material design. The Au NP–CNT electrode maintains its stability and sensitivity for up to 50 d, signifying its potential for advanced ion sensing. Additionally, integration with a mobile wireless data system highlights the versatility of the sensor for health applications.
In this study, we investigate the opportunity of using waste tire char as a cathode material for lithium-ion primary batteries (LPBs). The char obtained by carbonizing waste tires was washed with acid and thermally fluorinated to produce CFX. The structural and chemical properties of the char and CFX were analyzed to evaluate the effect of thermal fluorination. The carbon structure of the char was increasingly converted to CFX structure as the fluorination temperature increased. In addition, the manufactured CFX- based LPBs were evaluated through electrochemical analysis. The discharge capacity of the CFX reached a maximum of 800 mAh/g, which is comparable to that of CFX- based LPBs manufactured from other carbon sources. On the basis of these results, the use of waste tire char-based CFX as a cathode material for LPBs is presented as a new opportunity in the field of waste tire recycling.
본 연구에서는 현탁중합을 통해 이온교환입자를 합성하였다. 또한 음이온 교환막을 제조하기 위해 brominated poly(phenylene oxide) (Br-PPO)로 교환막 합성을 진행하였으며, 합성한 이온교환입자를 Br-PPO에 첨가하여 음이온 교환막 에 성능을 향상시키고자 하였고, 이를 적용하여 음이온 교환막 연료전지 시스템의 성능 평가를 진행했다. 이온교환입자는 FT-IR, TGA 및 UTM을 통해 구조 분석, 열적 기계적 특성을 평가하였다. Br-PPO는 NMR을 통해 화학적 구조 분석 및 합성 여부를 확인하였고, 음이온 교환막 연료 전지 셀 테스트를 진행하기 전 이온전도도와 이온교환용량, 팽윤도 및 수분함수율을 측정해 연구되고 있는 다른 음이온 교환막들과 비교를 통해 성능을 평가했다. 최종적으로 가장 성능이 우수했던 이온교환입 자를 0.7 wt%를 첨가한 Br-PPO-TMA- SDV 음이온 교환막을 연료전지 시스템에 도입하여 상용 막인 FAA-3-50과 성능을 비 교했다.
전고체 전지는 전기 자동차의 안정성을 향상시키기 위해 기존의 리튬 이온 전지를 대체할 주요 후보로 간주되고 있 습니다. 그러나 전고체 전지에 사용되는 황화물계 고체 전해질은 산화 환원 안정성이 부족하며 양극복합전극과 표면 에서 부반응을 이르켜 문제를 야기시킵니다. 때문에 양극 표면 코팅법이 제안되었고 이는 충방전 사이클 안정성 및 속도 특성의 개선에 유용한 효과를 나타낼 수 있습니다. 본 논문에서는 결정학적 분석을 통하여 신규 Li-Zr-O 조성 탐색을 하였고, 다양한 양극 소재 코팅소재 후보군 중 리튬 이온 전도체인 Li6Zr2O7 구조가 매우 유망하다는 연구 결 과를 확인했습니다. 본 논문은 기존에 사용되는 LiNbO3, Li4Ti5O12가 아닌 새로운 다양한 구조 및 조성의 양극 코팅 소 재개발에 대한 필요성 및 가능성을 시사합니다.
Measurement of oxide ion (O2-) concentration is a basic technology required in molten salt fields, from energy storage systems to electrolytic reduction of rare earth elements or spent nuclear fuels. In a molten salt reactor, O2- ions react with actinide elements to form their oxides or oxy-chlorides to induce actinide precipitation, and promote metal corrosion to cause a failure of structural material. For these reasons, removal of O2- ions and monitoring of the O2- concentration in molten salt reactors are essential. In this study, methods using chemical and electrochemical methods were investigated for measuring the concentration of O2- ions in a molten salts. The acid-base neutralization reaction was used as a chemical analysis method. And electrochemical methods using the O2- diffusion limit current and YSZ (yttria stabilized zirconia) indicator electrode were used for measuring the O2- concentration. Finally, a modified method using porous membrane electrode was applied to monitor the O2- concentration. The O2- concentration was measured up to about 2wt% of Li2O by the method using the O2- diffusion current, up to about 4wt% by the YSZ indicator electrode, and about 6wt% by the porous membrane electrode in LiCl molten salts.
The homogeneity of radioactive spent ion exchange resins (IERs) distribution inside waste form is one of the important characteristics for acceptance of waste forms in long-term storage because heterogenous immobilization can lead to the poor structural stability of waste form. In this study, the homogeneity of metakaolin-based geopolymer waste form containing simulant IERs was evaluated using a laser-induced breakdown spectroscopy (LIBS) and statistical approach. The cation-anion mixed IERs (IRN150) were used to prepare the simulant spent IERs contaminated by non-radioactive Cs, Fe, Cr, Mn, Ni, Co, and Sr (0.44, 8.03, 6.22, 4.21, 4.66, 0.48, and 0.90 mg/g-dried IER, respectively). The K2SiO3 solution to metakaolin ratio was kept constant at 1.2 and spent IERs loading was 5wt%. For the synthesis of homogeneous geopolymer waste form, spent IERs were mixed with K2SiO3 solution and metakaolin first, and then the fresh mixture slurry was poured into plastic molds (diameter: 2.9 cm and height: 6.0 cm). The heterogeneous geopolymer waste form was also fabricated by stacking two kinds of mixtures (8wt% IERs loading in bottom and 2wt% in top) in one mold. Geopolymers were cured for 7d (1d at room temperature and 6d at 60°C). The hardened geopolymers were cut into top, middle, and bottom parts. The LIBS spectra and intensities for Cs were obtained from the top and bottom of each part. Cs was selected for target nuclide because of its good sensitivity for measurement. Shapiro-Wilk test was performed to determine the normality of LIBS data, and it revealed that data from the homogeneous sample is normal distribution (p-value = 0.9246, if p-value is higher than 0.05, it is considered as normal distribution). However, data from the heterogeneous sample showed abnormal distribution (p-value = 7.765×10-8). The coefficient of variation (CoV) was also calculated to examine the dispersion of data. It was 31.3% and 51.8% from homogeneous and heterogeneous samples, respectively. These results suggest that LIBS analysis and statistical approaches can be used to evaluate the homogeneity of waste forms for the acceptance criterion in repositories.
Mixed-bed ion exchange resin consist of anion exchange resin and cation exchange resin is used to treat liquid radioactive waste in nuclear power plants. C-14 from heavy water reactors (HWR) is adsorbed on the anion exchange resin and is considered intermediate-level radioactive waste. The total amount of radioactivity of C-14 in spent ion exchange resin exceeds the activity limits for the disposal facility. Therefore, it is necessary to reduce the radioactivity through pre-treatment. There are thermal and non-thermal methods for the treatment of spent ion exchange resin. However, destructive methods have the problem of emitting off-gas containing radionuclides. To solve this challenge, various methods have been developed such as acid stripping, PLO process, activity stripping, thermal treatment and others. In this study, spent ion exchange resin (spent resin) was treated using microwave. The reaction characteristics of the resin to microwave were used to selectively remove the C-14 on the functional groups. Simulated spent anion exchange resin and spent resin from Wolseong NPP were treated with the microwave method, and the desorption rate was over 95%. An integrated process system of 1 kg/batch was built to produce operating data. After the operation of the process, characterization and evaluation of post-treatment for condensate water and adsorbent used in the process were performed. When the process system was applied to treat simulated spent resin and real spent resin, both showed a desorption rated of more than 97%. It means that the C-14 was successfully removed from the radioactive spent resin.
In concrete structures exposed to chloride environments such as seashore structures, chloride ions penetrate into the concrete. Chlorine ions in concrete react with cement hydrates to form Friedel’s salt and change the microstructure. Changes in the microstructure of concrete affect the mechanical performance, and the effect varies depending on the concentration of chloride ions that have penetrated. However, research on the mechanical performance of concrete by chloride ion penetration is lacking. In this study, the effect of chloride ion penetration on the mechanical performance of dry cask concrete exposed to the marine environment was investigated. The mixture proportion of self-compacting concrete is used to produce concrete specimens. CaCl2 was used to add chlorine ions, and 0, 1, 2, and 4% of the binder in weight were added. To evaluate the mechanical performance of concrete, a compressive strength test, and a splitting tensile strength test were performed. The compressive strength test was conducted through displacement control to obtain a stress-strain curve, and the loading speed was set to 10 με/sec, which is the speed of the quasi-static level. The splitting tensile strength test was performed according to KS F 2423. As a result of the experiment, the compressive strength increased when the chloride ion concentration was 1%, and the compressive strength decreased when the chlorine ion concentration was 4%. The effect of the chloride ion concentration on the peak strain was not shown. In order to present a stress-strain curve model according to the chloride ion concentration, the existing concrete compressive stress-strain models were reviewed, and it was confirmed that the experimental results could be simulated through the Popovics model.