Nuclear power plants use ion exchange resins to purify liquid radioactive waste generated while operating nuclear power plants. In the case of PHWR, ion exchange resins are used in heavy water and dehydration systems, liquid waste treatment systems, and heavy water washing systems, and the used ion exchange resins are stored in waste resin storage tanks. The C-14 radioactivity concentration in the waste resin currently stored at the Wolseong Nuclear Power Plant is 4.6×106 Bq/g, exceeding the low-level limit, and if all is disposed of, it is 1.48×1015 Bq, exceeding the total limit of 3.04×1014 Bq of C-14 in the first stage disposal facility. Therefore, disposal is not possible at domestic low/medium-level disposal facilities. In addition, since the heavy water reactor waste resin mixture is stored at a ratio of about 20% activated carbon and zeolite mixture and about 80% waste resin, mixture extraction and separation technology and C-14 desorption and adsorption technology are required. Accordingly, research and development has been conducted domestically on methods to treat heavy water waste resin, but the waste resin mixture separation method is complex and inefficient, and there are limitations in applying it to the field due to the scale of the equipment being large compared to the field work space. Therefore, we would like to introduce a resin treatment technology that complements the problems of previous research. Previously, the waste resin mixture was extracted from the upper manhole and inspection hole of the storage tank, but in order to improve limitations such as worker safety, cost, and increased work time, the SRHS, which was planned at the time of nuclear power plant design, is utilized. In addition, by capturing high-purity 14CO2 in a liquid state in a high-pressure container, it ensures safety for long-term storage and is easy to handle when necessary, maximizing management efficiency. In addition, the modularization of the waste resin separation and withdrawal process from the storage tank, C-14 desorption and monitoring process, high-concentration 14CO2 capture and storage process, and 14CO2 adsorption process enables separation of each process, making it applicable to narrow work spaces. When this technology is used to treat waste resin mixtures in PHWR, it is expected to demonstrate its value as customized, high-efficiency equipment that can secure field applicability and safety and reflect the diverse needs of consumers according to changes in the working environment.

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.

Ultra-violet (UV) light is one of abiotic stress factors and causes oxidative stress in plants, but a suitable level of UV radiation can be used to enhance the phytochemical content of plants. The accumulation of antioxidant phenolic compounds in UV-exposed plants may vary depending on the conditions of plant (species, cultivar, age, etc.) and UV (wavelength, energy, irradiation period, etc.). To date, however, little research has been conducted on how leaf thickness affects the pattern of phytochemical accumulation. In this study, we conducted an experiment to find out how the antioxidant phenolic content of kale (Brassica oleracea var. acephala) leaves with different thicknesses react to UV-A light. Kale seedlings were grown in a controlled growth chamber for four weeks under the following conditions: 20°C temperature, 60% relative humidity, 12-hour photoperiod, light source (fluorescent lamp), and photosynthetic photon flux density of 121±10 μmol m-2 s-1. The kale plants were then transferred to two chambers with different CO2 concentrations (382±3.2 and 1,027±11.7 μmol mol-1), and grown for 10 days. After then, each group of kale plants were subjected to UV-A LED (275+285 nm at peak wavelength) light of 25.4 W m-2 for 5 days. As a result, when kale plants with thickened leaves from treatment with high CO2 were exposed to UV-A, they had lower UV sensitivity than thinner leaves. The Fv/Fm (maximum quantum yield on photosystem II) in the leaves of kale exposed to UV-A in a low-concentration CO2 environment decreased abruptly and significantly immediately after UV treatment, but not in kale leaves exposed to UV-A in a high-concentration CO2 environment. The accumulation pattern of total phenolic content, antioxidant capacity and individual phenolic compounds varied according to leaf thickness. In conclusion, this experiment suggests that the UV intensity should vary based on the leaf thickness (age etc.) during UV treatment for phytochemical enhancement.

This study was conducted to investigate the growth characteristics of cucumber (Cucumis sativus L. ‘Joeunbaekdadagi’) and tomato (Solanum lycopersicum L. ‘Dotaerang Dia’) seedlings by light intensities and CO2 concentrations in a closed-type plant production system (CPPS). Cucumber and tomato seeds were sown in 50-cell trays and germinated in CPPS at air temperature 25 ± 1°C and relative humidity 50 ± 10% for 4 days. After germination, the CO2 concentrations and light intensity treatment were treated at 500 (ambient), 1,000, and 1,500 μmol·mol-1 and 100, 200, and 300 μmol·m-2·s-1 photosynthetic photon flux density (PPFD), respectively. The leaf area of cucumber showed the highest value in CO2 1,500 μmol·mol-1. However, the leaf area of the tomato had no significant difference in CO2 concentrations and light intensities treatments. In cucumber and tomato both seedlings, the growth and quality such as compactness and leaf area rate were increased with the increase of light intensity, and there were highest in 300 μmol·m-2·s-1. The root surface and number of root tips of cucumber and tomato seedlings were significantly increased with the increase in light intensity. In conclusion, the regulation of the CO2 concentrations and light intensity can control the growth and quality of cucumber and tomato seedlings in CPPS, especially, increasing the light intensity can improve more significantly the growth and quality of seedlings.

한국의 목조건축문화유산은 상당수가 산림에 인접하여 흰개미에 의한 피해에 취약하다. 국내 흰개미 방제법은 살충제 접촉을 통한 화학적 방제법이 주로 이용되며, 방제 기간을 단축하기 위해서는 흰개미를 빠르게 약제까지 유인시킬 방법이 필요하다. 본 연구에서는 한국 서식 흰개미 에 대한 유인물질로 이산화탄소를 선정하여 유인여부 및 적절한 유인농도를 탐색하였으며, 지중 환경에서의 유인효력 기초평가를 진행하였다. 평가를 통해 흰개미에 대한 이산화탄소의 유인 효과를 확인하였으며, 이산화탄소 농도 10% 이하의 유효한 범위를 선정하였다. 또한 지중에서의 유인 효과를 확인함으로써 지중 환경에서의 적용 가능성을 파악하였다. 향후 현장에서 이산화탄소의 적용방안을 연구함으로써, 목조건축문화유 산의 흰개미 방제 시 개선된 방제 효과를 가질 수 있을 것으로 사료된다.

Photocatalytic CO2 reduction is a promising approach for reducing CO2 emissions and achieving the goal of carbon neutrality. In this work, selectively coupling Cu(OH)2 and CuO with amine-modified brookite TiO2 ( NH2–B–TiO2) has been achieved by a simple precipitation method. The results show that CuO is better than Cu(OH)2 as a co-catalyst to enhance the CO2 photoreduction capability of NH2– B–TiO2. The highest rates of CO2 conversion to CH4 and CO of NH2– B–TiO2–CuO composite reach 6.05 and 3.25 μmol h− 1 g− 1, respectively, which is higher than 8 times the yield of CH4 of NH2– B–TiO2. It is proposed that the NH2– B–TiO2–CuO composite offers an effective charge transfer through the formation of a p–n junction between NH2– B–TiO2 and CuO interfaces, while in the NH2– B–TiO2–Cu(OH)2 composite, the Cu(OH)2 dominantly serves as an electron sink to capture photo-induced electrons, promoting photo-induced carrier separation. This work provides an ingenious synthetic method for selectively anchoring Cu(OH)2 and CuO on semiconductors with different charge transfer routes for an efficient CO2 photoreduction.

이 연구는 팬데믹(pandemic) 전후 국제항공여객 운송시장을 대상으로 항공편 운항에 의한 CO2 배출 특성과 변화를 체계적으 로 파악하는 것을 주요 목적으로 한다. 이를 위해 2019년과 2021년 2분기 전 세계 국제여객 항공편 스케줄 데이터를 기반으로 ICAO(International Civil Aviation Organization)의 CERT(CO2 Estimation and Reporting Tool) 인벤토리를 이용하여 노선 단위의 CO2 배출량을 추정한 후, 노선의 대권 거리와 항공기의 크기를 기준으로 구분된 하부시장에 따른 CO2 배출량과 배출 효율성의 분포와 변화를 비교분석하였다. 주요 분석 결과는 다음과 같다. 첫째, 2021년 2분기 전 세계 국제항공여객 운송시장의 CO2 배출량은 약 31.6백만 톤으로 추정되었으며. 2019년 동 분기(117.95백만 톤) 대비 약 73.21% 감소하였다. 두 시기 모두 5,000km 이상의 장거리 시장, 그리고 100~400석 항공기 운용 시장에서의 배출량 비중이 높게 나타났다. 다만 팬데믹 기간에는 5,000km 이상, 그리고 400석 이상 항공기 시장에서 CO2 배출량의 감소가 두드러지게 나타났다. 둘째, 2021년 2분기 시장의 CO2 배출 효율성은 2019년 동 분기 대비 약 4% 향상되었다. 두 시기 모두 노선의 대권 거리와 항공기의 크기가 증가할수록 배출 효율성이 감소하는 경향이 존재하였으며, 팬데믹 기간 중 일부 하부시장에서는 구형 및 초대형 기종들의 운항 감축(혹은 중단)이 두드러짐에 따라 배출 효율성이 향상되기도 하였다. 마지막으로 팬데믹 전후 주요 국제노선들의 CO2 배출 효율성 변화를 탐색한 결과, 글로벌 허브 공항들을 연결하는 대륙 간 장거리 노선들을 중심으로 효율성이 낮게 나타난 반면, 차상위 계층 공항들과 연결된 일부 노선들, 그리고 동남아･동북아의 주요 공항들을 연결하는 역내 노선들은 상대적으로 효율성이 높게 나타났다. 본 연구는 팬데믹 전후 전 세계 국제항공여객 운송시장의 운영 실적과 CO2 배출에 대한 세부 특성과 변화를 실증적으로 분석했다는 점에서 의의가 있다.

Physicochemical properties and storage stability of plant-based alternative meat prepared with low-fat soybean powder (LPAM) treated by supercritical-CO2 and those of full-fat soybean powder (FPAM) were compared. Ash and crude protein contents were higher in LPAM than in FRAM. Water absorption capacity and oil absorption capacity were significantly higher in LPAM than in FPAM. Water binding capacity was higher in LPAM than in FPAM during a 20 days storage period at 5℃ and pH was significantly lower in LPAM than in FPAM after a 5~10 days storage period. Hardness, gumminess and chewiness significantly increased with the increase in the storage period, and the three were significantly higher in LPAM than in FPAM after 10 days and 20 days of storage. The acid value showed no remarkable difference according to the storage period in LPAM; however, it was significantly higher in FPAM than in LPAM after 20 days of storage. The peroxide value and TBA value were significantly increased according to the storage period, and were significantly lower iin LPAM than in FPAM during all the storage periods. Therefore, the use of low-fat soybean powder may be effective in improving oxidative stability during storage in the production of plant-based alternative meat.

‘갑주백목’ (Diospyros kaki Thunb cv. Hachiya) 감은 현재 홍시 또는 건시로만 식용되고 있는데 탈삽된 생과로서의 활용이 기대된다. CO2 및 ethanol 탈삽 처리와 동시에 1-methylcyclopropene (1-MCP)를 처리하여 탈삽과 연화억제에 대한 효과를 보고자 본 연구를 수행하였다. CO2 탈삽은 20L 아크릴 용기를 이용하여 95% CO2를 24시간, ethanol 탈삽은 PE 필름(85.0cm×63.5cm)을 이용하여 99.9% ethanol 20ml를 3일간 상온(23℃)에서 처리하였다. 1-MCP는 탈삽 처리와 동시에 1μL･L-1을 처리하였다. 탈삽 처리 후 상온 모의유통과 3주 저온저장 후 상온 모의유통의 두 가지 조건에서 과실의 품질을 조사하였다. CO2는 처리 종료 후 2일에 ethanol은 5일에 식용이 가능한 상태로 탈삽 되었으며 탈삽이 완료되지 않은 과실은 3주간의 저온 저장에서 완전히 탈삽되었다. 1-MCP는 탈삽속도에는 큰 영향을 미치지 않았으며 CO2와 ethanol 탈삽 모두에서 우수한 연화억제 효과를 나타내었다. 특히, 3주 저온 저장 후 상온 유통에서 1-MCP의 연화억제 효과는 더욱 크게 나타났다. 이상의 결과로 볼 때 1-MCP는 감의 탈삽에 있어 별도의 처리시간을 필요로 하지 않는 효과적인 연화억제 수단으로 판단되며, 이러한 ‘갑주백목’ 탈삽 생과는 향후 국내 유통 및 해외 수출이 기대된다.

본 연구에서는 중공사형 지지체막을 폴리술폰(polysulfone, PSf) 고분자를 이용하여 비용매 상분리법(non solvent induced phase separation, NIPS)에 의해 제조하였다. 제조된 중공사 지지체막을 PDMS와 Pebax를 코팅하여 중공사형 복합막 을 제조하고 CO2, H2, O2 그리고 N2에 대한 순수 투과도(permeance)와 선택도를 측정하였다. 제조된 복합막 모듈 중에서 선 택도(CO2/H2)가 가장 높은 모듈을 선정하여 모사가스를 사용하여 스테이지컷(stage cut, SC)의 변화에 따라 분리성능을 측정 하였다. 이때 사용된 모사가스는 PSA에서 버려지는 off gas의 농도인 CO2 70% : H2 30%인 것을 사용하였다. 1단 실험에서 는 H2 농도 약 60%, H2 회수율 12%의 값을 얻을 수 있었다. 낮은 H2 농도와 회수율을 극복하기 위해 2단 직렬 테스트를 수 행하였으며, 이를 통해 H2 농도 약 70%, H2 회수율 70%를 달성할 수 있었으며, 이를 통해 CO2/H2 분리에 대하여 분리 공정 구성을 도출할 수 있었다.

In this work, subabul wood biomass was used to prepare carbon adsorbents by physical and chemical activation methods at various carbonization temperatures. The properties of the carbon adsorbents were estimated through characterization techniques such as X-ray diffraction, Fourier transform infrared spectroscopy, X–ray photo electron spectroscopy, laser Raman spectroscopy, scanning electron microscopy, CHNS-elemental analysis and N2 adsorption studies. Subabul-derived carbon adsorbents were used for CO2 capture in the temperature range of 25–70 °C. A detailed adsorption kinetic study was also carried out. The characterization results indicated that these carbons contain high surface area with microporosity. Surface properties were depended on treatment method and carbonization temperature. Among the carbons, the carbon prepared after treatment of H3PO4 and carbonization at 800 °C exhibited high adsorption capacity of 4.52 m.mol/g at 25 °C. The reason for high adsorption capacity of the adsorbents was explained based on their physicochemical characteristics. The adsorbents showed easy desorption and recyclability up to ten cycle with consistent activity.

In recent years, people are increasingly interested in CO2 hydrogenation to produce value-added chemicals and fuels ( CH4, CH3OH, etc.). In the quest for an efficient treatment in CO2 methanation and methanolization, several technologies have been practiced, and DBD plasma technology gain attention due to its easily handling, mild operating conditions, strong activation ability, and high product selectivity. In addition, its reaction mechanism and the effect of packing materials and reaction parameters are still controversial. To address these problems efficiently, a summary of the reaction mechanism is presented. A discussion on plasma-catalyzed CO2 hydrogenation including packing materials, reaction parameters, and optimizing methods is addressed. In this review, the overall status and recent findings in DBD plasma-catalyzed CO2 hydrogenation are presented, and the possible directions of future development are discussed.

1,3-다이옥솔란은 용매, 전해질 및 시약으로서 화학, 페인트 및 제약 산업에서 광범위한 관심을 받고 있는 화합물 이다. 1,3-dioxolane은 주로 독성, 발암성, 폭발성, 자동 인화성이 없으며 다기능성을 가지고 있어, 대부분의 유기 및 수성 용 매 조건에서 우수한 용해성을 가져 고분자 전구체로서 사용된다. 최근 몇 년 동안 이 물질은 배가스 및 천연 가스 혼합물에 서 CO2를 분리하기 위한 CO2 선택적 고분자 전구체로서 점점 더 많은 관심을 받고 있다. Poly(1,3-dioxolane) (PDXL)은 폴 리에틸렌 옥사이드(PEO)보다 높은 에테르 산소 함량을 가지고 있으며, 이는 극성 에테르 산소 그룹이 CO2에 대해 강한 친화 력을 나타내기 때문에 우수한 막 CO2/N2 분리 특성을 보인다. 따라서 PDXL 기반 분리막은 비극성(N2, H2 및 CH4) 가스에 대해 탁월한 CO2 용해도 선택성을 보인다. 그러나 PEO와 마찬가지로 PDXL의 극성기는 고분자 사슬의 밀집도를 증가시키고 고분자 결정화를 유발하여 기체 투과도를 감소시켜 이에 대한 개선이 필요하다. 이 논문에서는 기체 분리 응용 분야에서 PDXL기반 고분자막의 최근 발전과 한계에 대해 알아보고자 한다. 또한 CO2 분리 공정에서 1,3-dioxolane 기반 고분자의 한 계를 극복하기 위한 몇 가지 분자 설계방안에 대해 다루어 보기로 한다.

Porous carbons are considered promising for CO2 capture due to their high-pressure capture performance, high chemical/ thermal stability, and low humidity sensitivity. But, their low-pressure capture performance, selectivity toward CO2 over N2, and adsorption kinetics need further improvement for practical applications. Herein, we report a novel dual-templating strategy based on molten salts (LiBr/KBr) and hydrogen-bonded triazine molecules (melamine–cyanuric acid complex, MCA) to prepare high-performance porous carbon adsorbents for low-pressure CO2. The comprehensive investigations of pore structure, microstructure, and chemical structure, as well as their correlation with CO2 capture performance, reveal that the dual template plays the role of porogen for multi-hierarchical porous structure based on supermicro-/micro-/meso-/ macro-pores and reactant for high N/O insertion into the carbon framework. Furthermore, they exert a synergistic but independent effect on the carbonization procedure of glucose, avoiding the counter-balance between porous structure and hetero-atom insertion. This enables the preferred formation of pyrrolic N/carboxylic acid functional groups and supermicropores of ~ 0.8 nm, while retaining the micro-/meso-/macro-pores (> 1 nm) more than 60% of the total pore volume. As a result, the dual-templated porous carbon adsorbent (MG-Br-600) simultaneously achieves a high CO2 capture capacity of 3.95 mmol g− 1 at 850 Torr and 0 °C, a CO2/ N2 (15:85) selectivity factor of 31 at 0 °C, and a high intra-particle diffusivity of 0.23 mmol g− 1 min− 0.5 without performance degradation over repeated use. With the molecular scale structure tunability and the large-scale production capability, the dual-templating strategy will offer versatile tools for designing high-performance carbon-based adsorbents for CO2 capture.

Here, we report the preparation of microporous-activated carbons from a Brazilian natural lignocellulosic agricultural waste, cupuassu shell, by pyrolysis at 500 ºC and KOH activation under different experimental conditions and their subsequent application as adsorbent for CO2 capture. The effect of the KOH:precursor ratio (wt/wt%) and the activation temperature on the porous texture of activated carbons have been studied. The values of specific surface area ranged from 1132 to 2486 m2/ g, and the overall micropore volume ranged from 0.73 to 1.02 cm3/ g. Carbons activated with 2:1 ratio of KOH and activation temperature of 700 ºC presented a CO2 adsorption at 1 bar of 7.8 and 4.4 mmol/g at 0 °C and 25 ºC, respectively. The isosteric heat of adsorption, Qst , was calculated for all samples by applying the Clausius–Clapeyron approach to CO2 adsorption isotherms at both temperatures. The values of CO2 adsorption capacities are among the highest reported in the literature, especially for activated carbons produced from biomass.

Removing CO2 gas to address the global climate crisis is one of the most urgent agendas. To improve the CO2 adsorption ability of activated carbon, nitrogen plasma surface treatment was conducted. The effect of nitrogen plasma treatment on the surface chemistry and pore geometry of activated carbon was extensively analyzed. The porosity and surface groups of the activated carbon varied with the plasma treatment time. By plasma treatment for a few minutes, the microporosity and surface functionality could be simultaneously controlled. The changed microporosity and nitrogen groups affected the CO2 adsorption capacity and CO2 adsorption selectivity over N2. This simultaneous surface etching and functionalization effect could be achieved with a short operating time and low energy consumption.