Selenium (Se), a vital trace element found naturally, plays a pivotal role for human being in low concentrations. Notably, within the spectrum of essential elements, Se possesses the most restricted range between the dietary deficiency (< 40 μg day-1) and the acute toxicity (> 400 μg day-1). Therefore, it is of paramount importance to maintain bioavailable Se levels within permissible limits in our drinking water sources. Among the various Se species, inorganic variants such as selenite (SeO3 2-) and selenate (SeO4 2-) are highly water-soluble, with SeO3 2- being notably more toxic than SeO4 2-. Consequently, the primary focus lies in effectively sequestering SeO3 2- from aquatic environments. Numerous methods have been investigated for SeO3 2- adsorption, including the use of metal oxides and carbon-based materials. Especially, iron oxides have garnered extensive attention due to their water stability and environmentally friendly properties. Nevertheless, their limited surface area and insufficient adsorption sites impose constraints on their efficacy as materials for SeO3 2- removal. Recently, metal–organic frameworks (MOFs), composed of metal centers bridged by organic linkers have increasingly focused as promising adsorbents for SeO3 2- removal, offering significant advantages such as large surface areas, high porosities, and structural versatility. Furthermore, there is a growing interest in defective MOFs, where intentional defects are introduced into the MOF structure. This deliberate introduction of defects aims to enhance the adsorption capacity by increasing the number of available adsorption sites. In this context, herein, we present the Fe-BTC (BTC = 1,3,5-benzenetricarboxylic acid) synthesized via a post-synthetic metal-ion metathesis (PSMM) approach, which is one of the defect engineering methods applied to metal sites. We employ the well-established MOF, HKUST-1, known for its substantial surface area, as the pristine MOF. While the pristine MOF has a crystalline phase, during the PSMM process, Fe-BTC is transformed into an amorphous phase by allowing the introduction of numerous metal defect sites. These introduced metal defect sites serve as Lewis acidic sites, enhancing the adsorption capability for selenite. Furthermore, despite its amorphous nature, Fe-BTC exhibits a substantial surface area and porosity comparable to that of the crystalline pristine MOF. Consequently, Fe-BTC, distinguished by its numerous adsorption sites and its high porosity, demonstrates a remarkable capacity for selenite adsorption.

Owing to the rapid rise of global energy demands, the operation of nuclear power plants is still indispensable. However, following the nuclear accident at Fukushima-Daiichi in 2011, the secure sequestration of radioactive waste has become critical for ensuring safe operations. Among various forms of nuclear wastes, capturing radioactive organic iodide (ROIs, e.g., methyl iodide, ethyl iodide, and propyl iodide) as one of the important species in gas phase waste has been challenged owing to the insufficient sorbent materials. The environmental release of ROIs with high volatility can give rise to adverse effects, including the accumulation of these substances in the thyroid and the development of conditions such as hypothyroidism and thyroid cancer. Compared to an iodine molecule, ROIs exhibit low affinity for conventional sorbents such as Ag@mordenite zeolite and triethylenediamine-impregnated activated carbon (TED@AC), resulting in lower sorption rates and capacities. Furthermore, in conditions resembling practical adsorption environments with high humidity, the presence of H2O significantly impedes the adsorption process, leading to a nearly complete cessation of adsorption. To address these issues, metal-organic frameworks (MOFs) can be effective alternative sorbents owing to their high surface area and designable and tailorable pore properties. In addition, the wellfined crystalline structures of MOFs render in-depth study on the structure-properties relationship. However, there has been limited research on the adsorption of ROIs using MOFs, with the majority of adsorption processes relying on highly reversible physisorption. This type of ROIs adsorption not only exists in a precarious state that is susceptible to volatilization but also exhibits significantly reduced adsorption capabilities in humid environments. Thus, for the secure adsorption of the volatile ROIs, the development of sorbents capable of chemisorption is highly desirable. In this study, we focused on ROIs adsorption by electrophilic aromatic substitution with the electron-rich m-DOBDC4− (m-DOBDC4− = 4,6-dioxo-1,3-benzenedicarboxylate) present in Co2(m -DOBDC). The chemisorption of ROIs via electrophilic aromatic substitution not only leads to the formation of C-C bonds, ensuring stability but also triggers color changes in the crystal by interacting with open-metal sites and iodide ions. Leveraging these advantages, we developed an infrared radiation-based sensing method that demonstrates superior performance, exhibiting high adsorption capacities and rates, even under the challenging conditions of high-humidity practical environments.

Bisphenol-A, also known as BPA, is commonly used as a building block for epoxy and polycarbonate plastics. However, it has been recently identified as a major source of water pollution due to its release into the water from plastic products. BPA-based resins can also contaminate the water with high concentrations of BPA, which can enter the water bodies through production units and wastewater discharge. Photocatalysis, particularly the photo-Fenton process, is an effective method for wastewater treatment and degrading pollutants. Titanium dioxide (TiO2) is usually chosen based on its high photocatalytic properties and high performance. However, its wide band gap energy is a major issue for the photocatalytic process. This means that the catalyst can only exhibit high photocatalytic performance under UV-light irradiation and usually requires an acidic pH, which limits its use. In order to address the aforementioned issues, a visible-light photoactive photo-Fenton reaction has been successfully developed to degrade bisphenol A at natural pH using H2O2. The process was highly efficient, achieving complete degradation of phenol in just three hours of visible light irradiation with Cu-MOF. This environmentally friendly Fenton process has the advantage of occurring at natural pH levels with the presence of H2O2, providing a new perspective for efficient degradation. The photocatalyst was characterized using single X-ray diffraction (SC-XRD), powder X-ray diffraction (PXRD), Fourier Transform Infrared Spectroscopy (FTIR), and UV–vis diffuse reflectance spectroscopy (DRS).

The nuclear facilities at Korea Atomic Energy Research Institute (KAERI) have generated a variety of organic liquid radwaste and radiation levels are also varied. At KAERI, the organic liquid radwaste has been stored at Radioactive Waste Treatment Facility (RWTF) temporarily due to the absence of the recognized treatment technique while inorganic liquid radwaste can be treated by evaporation, bituminization, and solar evaporation process. The organic liquid radioactive waste such as spent oil, cutting oil, acetone, ethanol, etc. was generated from the nuclear facilities at KAERI. Among the organic liquid radioactive wastes, spent oil is particularly significant. According to the nuclear safety act, radioactive waste can be cleared by incineration and landfilling if it meets the criteria of less than 10 μSv/h for individual dose and 1 person – Sv/y for collective dose. Dose assessment was performed on some organic liquid radioactive waste with a very low possibility of radioactive contamination stored in RWTF at KAERI. As a result, it was confirmed that some wastes met the regulatory clearance standards. Based on this, it was approved by the regulatory body, and this became the first case in Korea and KAERI for permission for regulatory clearance of organic liquid radioactive waste by landfill after incineration.

Various types of solidifying materials are used to stabilize and solidify low and intermediatelevel radioactive dispersible waste. Portland cement is generally used to solidify various radioactive wastes because its facilities and processes are simple, less dangerous, and it has excellent compressive strength after curing compared to other materials. However, it is difficult to use Portland cement in radioactive waste containing highly water-soluble harmful substances such as sodium fluoride because it is prone to leaching harmful ingredients in immersion tests due to its low water resistance. In this study, solidification was achieved using an organic-inorganic hybrid solidifying binders consisting of inorganic binders such as Portland cement, blast furnace slag powder, silica fume, and organic binders such as epoxy resin. This material was then compared with a solidification material made of Portland cement alone. The mixing ratio of inorganic binders, water, and organic binders to simulated waste is 35%, 20%, and 25%, respectively. The mixing ratio of inorganic binders and water when using only Portland cement for simulated waste is 100% and 80%, respectively. The mixed paste was poured into a cylinder mold (Φ 5 × 10 cm) to seal the upper part, cured at room temperature for 28 days to produce a solidification specimen, and then subjected to various tests were performed, including compressive strength, immersion compressive strength, hydration peak temperature, length change, and immersion weight change. The compressive strength of the organic-inorganic hybrid solidification test was 13-17 MPa, the immersion compressive strength was 15-18 MPa, the hydration peak temperature was 33-36°C, the length change rate was -0.086%, and the immersion weight change rate was –2.359%. The compressive strength of the Inorganic solidification test using only Portland cement was 16-18 MPa, the immersion compressive strength was 20-21 MPa, the hydration peak temperature was 23-25°C, the length change rate was -0.150%, and the immersion weight change rate was -5.213%. The compressive strength and immersion compressive strength of the organic-inorganic hybrid solidification materials were slightly lower compared to those of Portland cement solidification materials, they still met the compressive strength standard of 7-12 MPa, taking into consideration the strength reduce and economic feasibility of the core drill process. Furthermore, it indicates that the rates of change in length and immersion weight decreased to about 1% and 5%, suggesting an improvement in water resistance. The above results suggest that applying the organic-inorganic hybrid solidification method to radioactive waste treatment can effectively improve water resistance and help secure long-term stability.

This work describes Ni–Ce–Cu metallic–organic framework (MOF) for the detection of non-essential amino acid l-cysteine. The tri-metallic Ni–Ce–Cu MOF was synthesized via a solvothermal method. The cyclic voltammetry and the differential pulse voltammetry techniques were used to examine the electrochemical detection of l-cysteine. The Ni–Ce–Cu MOF shows an oxidation peak in PB solution at pH 3.0 between the potential range of 0.0 and 0.7 V and strong electro-catalytic activity toward the oxidation of l-cysteine across a wide linear range of 0.1 to 250 nM and low detection limit (LOD) was calculated of 1.56 nM. The analysis of l-cysteine in milk and egg yolk samples showed with recovery range of 96.75–103.5% and 97.78–99.43% with RSD% of 2.3–3.2% and 2.7–7.2%, respectively. These results show the Ni–Ce–Cu MOF has high selectivity for l-cysteine detection in milk and egg samples.

In recent years, supercapacitors have attracted extensive attention due to their advantages such as fast charge and discharge rate, high power density and long cycle life. Because of its unique porous structure and excellent electrochemical properties, heteroatom-doped porous carbon (HPC) is deemed as a promising electrode material for supercapacitors. However, it is a great challenge to synthesize electrode materials with large surface area, ultra-high porosity and good electrochemical performance. In this work, two-dimensional conjugated microporous polymers (CMPs) containing ketones were synthesized by a simple one-step coupling reaction and used as carbon precursors. A series of samples (CMP-Ts) were prepared with the procedures of coupling reaction and carbonization. The optimized carbon material has high specific surface area (up to 2229.85 m2 g− 1), porous structure, high specific capacitance (375 F g− 1 at 0.5 A g− 1), and good cycling stability (capacitance retention of 98.8% after 1000 cycles at 5 A g− 1). Further, the supercapacitor has an energy density of 28.8 Wh kg− 1 at a power density of 5000 W kg− 1. This work lays a foundation for the preparation of carbon materials using microporous polymer as a precursor system, provides a new way of thinking, and demonstrates a great potential of high-performance supercapacitors.

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.

Bioreactors are devices used by sewage treatment plants to process sewage and which produce active sludge, and sediments separated by solid-liquid are treated in anaerobic digestion tanks. In anaerobic digestion tanks, the volume of active sludge deposits is reduced and biogas is produced. After dehydrating the digestive sludge generated after anaerobic digestion, anaerobic digested wastewater, which features a high concentration of organic matters, is generated. In this study, the decomposition of organic carbon and nitrogen was studied by advanced oxidation process. Ozone-microbubble flotation process was used for oxidation pretreatment. During ozonation, the TOC decreased by 11.6%. After ozone treatment, the TOC decreased and the removal rate reached 80.4% as a result of the Ultra Violet-Advanced Oxidation Process (UV-AOP). The results with regard to organic substances before and after treatment differed depending on the organic carbon index, such as CODMn, CODCr, and TOC. Those indexes did not change significantly in ozone treatment, but decreased significantly after the UV-AOP process as the linkage treatment, and were removed by up to 39.1%, 15.2%, and 80.4%, respectively. It was confirmed that biodegradability was improved according to the ratio of CODMn to TOC. As for the nitrogen component, the ammonia nitrogen component showed a level of 3.2×102 mg/L or more, and the content was maintained at 80% even after treatment. Since most of the contaminants are removed from the treated water and its transparency is high, this water can be utilized as a resource that contains high concentrations of nitrogen.

유기농 생태농업단지 논에서 출현하는 수서곤충의 생태자원 분포 특성을 비교하고자 유기농 단지 논에 둠벙 이 있는 조건과 둠벙이 없는 조건에서의 수서곤충상을 조사하여 관행 논의 분포 특성을 비교하였다. 수서곤충 출현은 둠벙이 있는 유기농 논 5목 15과 26종 413개체, 둠벙이 없는 유기농 논 5목 14과 22종 236개체, 관행 논 5목 11과 16종 155개체로 유기농 논에서 관행 논에 비해 수서곤충의 출현 과, 종 및 출현 개체수가 많았고, 유기농 논에서도 둠벙이 있는 조건에서 종수 및 개체수가 많음을 확인하였다. 특히 잠자리목의 경우 유기농 논 4과 8종 134개체, 둠벙이 없는 유기농 논 3과 5종 35개체, 관행 논 2과 4종 12개체로 전체 출현 종의 발생특성과 유사한 경향을 보였는데, 유기농 재배의 특성상 농약의 피해로부터 수서곤충에 안전한 환경이 조성된 점과 둠벙의 담수 및 다양한 수서생물의 발생으로 수서곤충의 서식조건에 유리하게 작용되었다고 보인다. 반면 파리목에서는 둠벙이 있는 유기농 논 3과 3종 18개체, 둠벙이 없는 유기농 논 3과 3종 25개체로 관행 논 2과 2종 24개체보다 발생양상이 다른 수서곤충에 비해 상대적으로 낮고, 관행 논보다 깔다구류의 개체수 19개체보다 각각 6개체, 12개체로 적게 출현한 점에서 유기농 재배유형과 둠벙의 서식처 제공이 수서곤충의 출현 및 분포에 건전성을 조장하는 방안이라고 판단된다.

유기농 논이용 콩-밀 생산체계에서 재배유형별 밀 파종 전 경운여부에 따라 경운/무경운 처리, 콩 재배시 비닐 피복 여부에 따라 피복/무피복 처리, 논의 생태적 개선 여부에 따라 개선/대조구 처리로 시험구를 조성하여 밀 재배 중 곤충자원의 출현 및 분포특성을 조사 비교하였다. 출현 곤충의 총 종수는 20종으로 경운 14종, 무경운 14종으로 차이는 없었고 피복 14종, 무피복 16종이었으며 개선구 18종, 대조구 13종으로 개선처리에서 곤충 출현 종수가 많았다. 출현 곤충의 총개체수는 경운 124개체, 무경운 76개체로 경운처리에서 많았고, 피복 100개체, 무피복 100개체로 차이가 없었으며 경운-무피복-개선에서 40개체로 가장 많았다. 유기농 밀에 피해를 주는 해충 으로 노린재류는 갈색날개노린재가 가장 많이 발생하였고, 메추리노린재, 시골가시허리노린재도 출현하였으 며 재배유형별 발생 개체수는 경운 81마리, 무경운 39마리로 경운에서 많았고, 무경운-피복-대조(7) = 무경운-무 피복-대조(7) < 무경운-무피복-개선(9) < 경운-피복-개선(12) < 경운-무피복-대조(13) < 무경운-피복-개선(16) < 경운-피복-대조(27) < 경운-무피복-개선(29) 순으로 발생하였다.