유기농업자재 제조 원료가 되는 주요 식물인 제충국, 고삼, 데리스, 님 등은 대부분 수입에 의존하고 있는 실정 으로 제품수급, 효용성 및 안전성 등에 빈번한 문제가 발생되고 있다. 이러한 문제점을 해결하기 위하여 국내 자생식물을 추출물 원료로 이용하기 위한 연구를 수행하고 있다. 이중 마트린이 함유되어 살충제로 이용되고 있는 고삼에 흰가루병, 총채벌레, 줄붉은들명나방, 담배거세미나방, 거품벌레류가 발생하여 피해를 주었다. 특 히 줄붉은들명나방(Uresiphita prunipennis)은 7월 하순부터 9월 중순까지 발생하여 엽육을 갉아먹고 엽맥만 남기는 피해를 주었고, 피해주율은 11% 였다. 이를 방제하기 위해 18종의 유기농업자재의 살충효과를 조사한 결과 주성분이 마늘추출물 80%, 데리스추출물 70% 등인 자재 6종이 80% 이상의 살충률을 나타내었다.

Because Scotinophara lurida has the habit of living under the rice plant, an introduction of a method for efficient control when spraying eco-friendly organic materials is needed. In this study, we investigated the density of S. lurida in drained- and irrigated-paddy field after spraying an organic material containing garlic bulb extracts, which has high insecticidal activity in S. lurida in direct spraying test in glass tube. As a result, an irrigated rice paddy showed a control effect of 66.4% after 3 days of spraying and 86.2% after 7 days, while a drained rice paddy showed a control effect of 33.9% after spraying and 61.9% after 7 days. These results suggest that effective control can be achieved in irrigated rice fields if organic farming materials are evenly sprayed and reach to the body of S. lurida. It is remained to study how irrigated water do contribute to increase the insecticidal effect in the future.

참깨는 건전 유기 종자생산을 위해서는 Corynespora cassicola 등과 같은 종자전염 병원균의 감염을 최소화해 야 하므로 비가림하우스 내에서의 종자생산이 필수적이다. 그러나 비가림하우스 재배 시 진딧물의 대발생으로 참깨의 생산량 저하 되므로 본 연구에서는 참깨 비가림하우스 내 유기 재배 시, 진딧물에 대한 효과적인 유기농업 자재를 선발하고자 한다. 등록된 유기농업자재 8종 중 4종을 기내에서 선발하였으며 선발된 유기농업자재 4종을 참깨 재배기간 중 주 1회 처리한 결과, 처리 간 유의한 차이가 나타났다. 수확기인 8월 3일 기준 무처리구 대비 데리스추출물 70%와 데리스 20%+시트로넬라 30%+계피추출물 10%은 12.3%, 9.0%만이 고사하여 우수한 방제 효과를 나타냈다. 본 연구 결과는 참깨 재배 시 농림현장에서 발생하는 복숭아혹진딧물에 대한 유기농업자재 효과를 검정함으로써 유기재배 농가의 자재 선택에 대한 정보를 제공하고자 한다

본 연구에서는 영종도에 위치한 인천과학고등학교 주변에 서식하는 개미와 개미집 근권토양을 두 차례에 걸쳐 채취한 것을 활용하여 토양미생물 순수분리 및 동정을 진행하였다. 채취된 개미의 더듬이의 모양, 털의 위치 및 분포 등의 형태학적 동정 및 DNA extraction을 통한 분자생물학적 동정을 통하여 채취한 개미를 Camponotus japonicus으로 결론하였다. 토양미생물을 연속희석법을 이용하여 확인한 결과 채취한 개미집 세 곳에서 각각 12, 18, 10개의 종이 동정되었다. 개미집 근권토양의 비옥도가 상대적으로 높다는 선행연구를 바탕 으로 ‘분리한 토양미생물이 다양한 유기물 분해 효소활성을 보일 것’이라는 가설을 세웠고, 이를 확인하기 위해 분별배지를 제작하여 디스크 확산법을 진행하였다. 실험 결과 개미집 근권 토양에서 분리된 균주가 일반 토양에 서 분리된 균주에 비해 높은 효소활성을 보임을 확인하였으며 개미집 근권 토양 미생물의 불용성인산 가용화능 이 우수함을 확인하였다. 이후 위 실험들을 바탕으로 개미집 근권 토양 미생물이 식물 생장을 촉진시켜 미생물을 접종한 토양에서의 식물의 건조 질량이 증가하였음을 확인하였다.

The disposal of organic pollutants is one of the important research topics. Some of the studies in this field are based on the degradation of organic pollutants with a catalytic agent. The cobalt tetraoxide/peroxymonosulfate system is an important catalytic system used for the radical degradation of organic pollutants. To increase the catalytic efficiency of such reactions, graphitization of activated carbon used as a support solid and nitrogen doping to the carbon structure are commonly used methods. In this study, cobalt tetraoxide production, N-doping and graphitization were carried out in a single step by heat treatment of activated carbon doped with the phthlocyanine cobalt (II) complex. The catalytic performance of the catalyst/ peroxymonosulfate system was investigated by changing the pH, catalyst, and PMS concentration parameters on rhodamine B and 1,3,5 trichlorophenol, which were used as models. It was seen that the catalysts had 97% activity on rhodamine B in 16 min and 100% on 1,3,5 trichlorophenol in 6 min. It was observed that the catalysts continued to show high catalytic activity for five cycles in reusability studies and had a very low cobalt leaching rate. These results are in good agreement with previously published studies. In line with these results, the synthesized N-doped graphitic carbon/Co3O4 catalyst can be used as an effective catalyst for wastewater treatments.

공유 유기 프레임워크(COF)는 분자 분리, 염료 분리, 가스 분리, 여과 및 담수화를 포함한 다양한 응용 분야에서 가능성을 보여주었습니다. COF를 막에 통합하면 투과성, 선택성 및 안정성이 향상되어 분리 공정이 향상됩니다. 단일 벽 탄 소 나노튜브(SWCNT)와 COF를 결합하면 염료 분리에 이상적인 높은 투과성과 안정성을 가진 나노 복합막을 생성합니다. COF를 폴리아미드(PA) 막에 통합하면 합성 계면 전략을 통해 투과성과 선택성이 향상됩니다. 혼합 매트릭스 막(MMM)의 3 차원 COF 필러는 CO2/CH4 분리를 향상시켜 바이오가스 업그레이드에 적합합니다. COF와 금속 유기 프레임워크(MOF) 막 을 결합한 모든 나노 다공성 복합재(ANC) 막은 투과성-선택성 트레이드오프를 극복하여 가스 투과성을 크게 향상시킵니다. 가상 COF (hypoCOF)를 사용한 계산 시뮬레이션은 CO2 분리 및 H2 정제와 관련하여 우수한 CO2 선택성과 작업 능력을 입 증합니다. 박막 복합재(TFC) 및 폴리술폰아미드(PSA) 막에 통합된 COF는 유기 오염물, 염 오염물 및 중금속 이온에 대한 거 부 성능을 향상시켜 분리 능력을 향상시킵니다. TpPa-SO3H/PAN 공유 유기 프레임워크 막(COFM)은 대전된 그룹을 활용하 여 정전기적 반발을 통해 효율적인 담수화를 가능하게 함으로써 기존의 폴리아미드 막에 비해 우수한 담수화 성능을 보여 이 온 및 분자 분리의 잠재력을 제시했습니다. 이러한 연구 결과는 투과성, 선택성 및 안정성을 향상시켜 향상된 분리 공정을 위 한 막 기술에서 COF의 잠재력을 강조합니다. 이 검토에서는 분리 공정에 적용된 COF에 대해 논의합니다.

Thermoelectric (TE) energy harvesting, which converts available thermal resources into electrical energy, is attracting significant attention, as it facilitates wireless and self-powered electronics. Recently, as demand for portable/wearable electronic devices and sensors increases, organic-inorganic TE films with polymeric matrix are being studied to realize flexible thermoelectric energy harvesters (f-TEHs). Here, we developed flexible organic-inorganic TE films with p-type Bi0.5Sb1.5Te3 powder and polymeric matrices such as poly(3,4-eethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and poly (vinylidene fluoride) (PVDF). The fabricated TE films with a PEDOT:PSS matrix and 1 wt% of multi-walled carbon nanotube (MWCNT) exhibited a power factor value of 3.96 μW ‧ m-1 ‧ K-2 which is about 2.8 times higher than that of PVDF-based TE film. We also fabricated f-TEHs using both types of TE films and investigated the TE output performance. The f-TEH made of PEDOT:PSS-based TE films harvested the maximum load voltage of 3.4 mV, with a load current of 17.4 μA, and output power of 15.7 nW at a temperature difference of 25 K, whereas the f-TEH with PVDF-based TE films generated values of 0.6 mV, 3.3 μA, and 0.54 nW. This study will broaden the fields of the research on methods to improve TE efficiency and the development of flexible organic-inorganic TE films and f-TEH.

The current research introduces a novel relationship between consumer attitudes toward time and consumer well-being, connected to organic food consumption based on the findings from 206 American consumers. Consumer motivations to seek nutritional information appears as a mediator impacting organic food purchase intentions. Practical and theoretical implications are discussed.

How to effectively deal with the polluted water by the pollutant of organic dyes is the world problem. It is of great significance if the organic dyes in the polluted water can be directly turned into the useful materials through a facile approach. Herein, the water which contains the common organic dye, Reactive red 2 (RR2), has been chosen to be the model to synthesize graphene quantum dots (GQDs) by a facile route. The comprehensive characterizations, including TEM (HRTEM), XPS, Raman, PL and UV–Vis. spectra, have been performed to confirm the structures and explore the properties of the synthesized GQDs. Meanwhile, the excellent PL properties and low biotoxicity of the GQDs confer them with the potential applications in the biological fields. When the GQDs are excited by the wavelength of 360 nm, the maximum emission is achieved at 428 nm. It is well demonstrated that the synthesized GQDs are able to detect the Al3+ which causes multiple diseases, such as Parkinson, Alzheimer, kidney disease, and even cancer. The detection range is from 90 to 800 μM, which is different from the reported kinds of the literature. Therefore, this work not only provides an economical and environmental route on solving the universal problem from organic dyes, but also facilitates to advancing the synthesis and application of GQDs.

Volatile organic compounds (VOCs) are a paramount factor in air pollution of the environment. VOCs are vastly present in the wastewater discharged by the pharmaceutical industries. As it is evaporative in nature, it enters the environment spontaneously and causes air pollution, global warming, acid rain and climate change. VOCs must be treated before discharging or any other aerobic methods using an efficient catalyst. As the catalytic oxidation in the liquid phase is facile compared to the gas phase, this study investigated on catalytic liquid-phase oxidation of VOCs in model and real pharmaceutical wastewater. The model compounds of toluene-, ethylbenzene- and chlorobenzene-contaminated waters were treated separately along with the VOCs present in real pharmaceutical wastewater using a tungsten-based carbon catalyst. The tungsten was impregnated on the low-cost activated carbon matrix as it has good selectivity and catalytic property toward VOCs for facile catalytic operations. The metal catalysts were characterised by Fourier transform infrared spectroscopy, X-ray diffraction studies, and scanning electron microscopy with elemental and mapping analysis. The treatability was monitored by total organic carbon, ultra-violet spectroscopy and high-pressure liquid chromatography analysis. The tungsten-impregnated activated carbon matrix (WACM) has a catalytic efficiency toward toluene by 85.45 ± 1.78%, ethylbenzene by 93.9 ± 1.16%, chlorobenzene by 85.9 ± 2.26% and pharmaceutical VOCs by 85.05 ± 1.73% in 20 treatment cycles. The results showed that WACM worked efficiently in VOCs treatment, preventing the environment from air pollution. Furthermore, liquid-phase oxidation could easily be implementable on an industrial scale.

The emission of off-gas streams from used fuel recycling is a concern in nuclear energy usage as they contain radioactive compounds, such as, 3H, 14C, 85Kr, 131I, and 129I that can be harmful to human health and environment. Radioactive iodine, 129I, is particularly troublesome as it has a half-life of more than 15 million years and is prone to accumulate in human thyroid glands. Organic iodides are hazardous even at very low concentrations, and hence the capture of 129I is extremely important. Dynamic adsorption experiments were conducted to determine the efficiency of sodium mordenite, partially exchanged silver mordenite, and fully exchanged silver mordenite for the removal of methyl iodide present at parts per billion concentrations in a simulated off-gas stream. Kinetic analysis of the system was conducted incorporating the effects of diffusion and mass transfer. The possible reaction mechanism is postulated and the order of the reaction and the values of the rate constants were determined from the experimental data. Adsorbent characterization is performed to investigate the nature of the adsorbent before and after iodine loading. This paper will offer a comprehensive understanding of the methyl iodide behavior when in contact with the mordenites.

We used the measurement data derived from a proton transfer reaction time-offlight mass spectrometry (PTR-ToF-MS) to ascertain the source profile of volatile organic compounds (VOCs) from 4 major industrial classifications which showed the highest emissions from a total of 26 industrial classifications of A industrial complex. Methanol (MOH) was indicated as the highest VOC in the industrial classification of fabricated metal manufacture, and it was followed by dichloromethane (DM), ethanol (EN) and acetaldehyde (AAE). In the industrial classification of printing and recording media, the emission of ethylacetate (EA) and toluene (TOL) were the highest, and were followed by acetone (ACT), ethanol (EN) and acetic acid (AA). TOL, MOH, 2-butanol (MEK) and AAE were measured at high concentrations in the classification of rubber and plastic manufacture. In the classification of sewage, wastewater and manure treatment, TOL was the highest, and it was followed by MOH, H2S, and ethylbenzene (EBZ). In future studies, the source profiles for various industrial classifications which can provide scientific evidence must be completed, and then specified mitigation plans of VOCs for each industrial classification should be established.

Polymeric carbon nitride (p-C3N4) is a promising platform as a metal-free photo-catalyst for various reactions. The p-C3N4 can be produced by thermal poly-condensation of organic precursors. Their morphological and chemical structures depend on reaction conditions during the poly-condensation. In this study, two p-C3N4 materials are produced by heat treatment of urea under different gaseous conditions with air (urea-derived carbon nitride under air, UCN-A) and N2 (UCN-N), respectively. UCN-A and UCN-N samples are mesoporous materials and show excellent photocatalytic activities for degrading rhodamine B, an organic pollutant, under the irradiation of visible light. The UCN-A shows the better photocatalytic activity than UCN-N. Various characterizations reveal that more porous structures and larger surface areas of UCN-A are reasons for the better photocatalytic performance.

The organic complexing agents such as ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), and isosaccharinic acid (ISA) can enhance the radionuclides’ solubility and have the potential to induce the acceleration of radionuclides’ mobility to a far-field from the radioactive waste repository. Hence, it is essential to evaluate the effect of organic complexing agents on radionuclide solubility through experimental analysis under similar conditions to those at the radioactive waste disposal site. In this study, five radionuclides (cesium, cobalt, strontium, iodine, and uranium) and three organic complexing agents (EDTA, NTA, and ISA) were selected as model substances. To simulate environmental conditions, the groundwater was collected near the repository and applied for solubility experiments. The solubility experiments were carried out under various ranges of pHs (7, 9, 11, and 13), temperatures (10°C, 20°C, and 40°C), and concentrations of organic complexing agents (0, 10-5, 10-4, 10-3, and 10-2 M). Experimental results showed that the presence of organic complexing agents significantly increased the solubility of the radionuclides. Cobalt and strontium had high solubility enhancement factors, even at low concentrations of organic complexing agents. We also developed a support vector machine (SVM) model using some of the experimental data and validated it using the rest of the solubility data. The root mean square error (RMSE) in the training and validation sets was 0.012 and 0.016, respectively. The SVM model allowed us to estimate the solubility value under untested conditions (e.g., pH 12, temperature 30°C, ISA 5×10-4 M). Therefore, our experimental solubility data and the SVM model can be used to predict radionuclide solubility and solubility enhancement by organic complexing agents under various conditions.

Low- and intermediate-level radioactive waste for permanent disposal often contains organic complexing agents, so-called chelating agents. Organic complexing agents, which are polycarboxylic acids, can increase the mobility of radionuclides into the environment by forming water-soluble complexes with most heavy metals. Therefore, analyzing the complexing agents in radioactive waste is crucial for comprehensive management of nuclear wastes. According to regulatory guidelines, specifically Notice No. 2021-16 issued by the Nuclear Safety and Security Commission, the determination of chelating agent content in radioactive waste materials is required to ensure proper management and safe disposal. However, only a few methods are available to analyze the chelators in various matrices such as concrete, metals, soil, and mixed solid wastes like plastics, vinyl, and rubber. Recently, we found a UV-Vis method based on an enzymatic reaction is inadequate for analyzing citric acid in radioactive waste with a complex matrix like concrete. To address this, we developed a method to determine the contents of EDTA and NTA using a UV-Vis spectrophotometer and citric acid using ion chromatography. The results showed good validity and reliability to determine the chelating agents in various radioactive wastes.

The removal of aqueous pollutants, including dye molecules from wastewater remains one of the pressing problems in the world. Because of chemical stability and conjugated structure, dye molecules cannot be easy decomposed by heat with oxidizing reagents such as H2O2 and light. The most common representative of widespread organic pollutant is methylene blue (MB) with molecular formula C16H18ClN3S, which is important colorant and used in various chemical and biological production industries and causes serious environment problems. Porous materials, including MOFs (metal-organic frameworks) have been applied for efficient MB photocatalytic degradation. However, one of the main barriers to using most MOFs to break down aromatic organics is wide band gap energy, which means that the catalyst can exhibit high photocatalytic performance only under UVlight irradiation. Moreover, most MOFs usually show the poor water stability of frameworks, which tend to dissolve in water with total destruction. In this work we report about two new copper based MOFs with high photocatalytic properties for efficient MB degradation from wastewater under UV-light and natural sunlight. Time, required for 100% MB degradation, equals 7 minutes under UV (source 4 W 254 nm VL-4.LC UV-lamp) and 60 minutes under natural sunlight irradiation in the presence of H2O2. Crystal structure information is provided using single crystal X-ray diffraction data. The composition and comparative characteristics of MOFs are given using powder X-ray diffraction, UV–visible diffuse reflectance spectroscopy, UVvisible spectroscopy and Fourier-transform infrared spectroscopy.

Radioactive products generated by long-term operation at NPP can become deposited on the surfaces of the system and equipment, leading to radiation exposure for workers during the decommissioning process. Chemical decontamination is one of the methods to reduce radiation exposure of workers, and there are HP CORD UV, CITROX, CAN-DECON. In the chemical decontamination process, organic acids are generally used, and representative organic acids include oxalic acid and citric acid. There are various methods for removing residual organic acid in decontamination liquid waste, such as using an oxidizing agent and an ion exchange methods. However, there is a problem in that oxidizing agent is used excessively or secondary wastes are generated in excess during organic waste treatment. However, when organic acid is decomposed using a UV lamp, the amount of secondary waste is reduced because it tis decomposed into CO2 and H2O. In this study, organic acid decomposition was evaluated as the contact time of the UV lamp. The experimental equipment consists of a UV reactor, a mixing tank, a circulation pump. The experimental conditions involved preparing 60 L of organic liquid waste containing oxalic acid, hydrogen peroxide and iron chloride. Test A was conducted using one UV reactor, and Test B was performed by connecting two UV reactors in series. As a result of the experiment, a decomposition rate of over 95% was shown after one hour for oxalic acid, and it was confirmed that the initial decomposition rate was faster as the contact time increases. Therefore, in order to increase the initial decomposition rate, it is necessary to increase the contact time of the UV lamp by connecting the UV reactors in series.