The hybridization of graphene with magnetic nanoparticles has endowed graphene with increasing interest as the adsorbent for wastewater treatment. However, its fabrication often involves a multi-stepped chemical synthesis process. In this work, we demonstrate a facile, one-step, and solvent-free approach to fabricate Fe3O4 nanoparticle-anchored Laser-Induced Graphene ( Fe3O4@LIG) as an efficient adsorbent by direct laser irradiation on a ferric acetylacetonate containing polybenzoxazine film. Raman and X-ray diffraction analysis confirm the graphene component in the adsorbent, and the morphology characterizations show that Fe3O4 nanoparticles are distributed uniformly on LIG with hierarchical meso- and macro-porous structures. Adsorption experiments indicate that Fe3O4@ LIG can adsorb methylene blue (MB) from aqueous solutions in a fast and effective manner, with a maximum adsorption capacity up to 350.9 mg/g. The adsorption kinetics and isotherms are also investigated, which are well-described by the pseudo-second-order model and Langmuir model, respectively. Additionally, Fe3O4@ LIG is also demonstrated with the efficient removal of a variety of organic solvents from water. The favorable adsorption behavior of Fe3O4@ LIG is attributed to its unique porous structure and the molecular interactions with adsorbates. On the other hand, Fe3O4@ LIG has high magnetic property, and therefore, it could be easily recovered from water and well regenerated for repeated use. With the efficient adsorption of organic pollutants, magnetic separability, and good

Activated carbon fibers (ACFs) were treated by electroless plating of CuO to improve their removal performance for volatile organic compounds (VOCs). The properties of these samples(CuO@ACFs) were evaluated by X-ray photoelectron spectroscopy (XPS), BET and N2O chemisorption to determine the area and dispersion of metallic CuO. The removal efficiency for benzene was investigated by gas chromatography (GC). The breakthrough time of CuO@ACFs increased by approximately 120% compared to that of untreated ACFs at benzene of 100 ppm. CuO@ACFs removed 100% of the benzene in 20 h, indicating this material can be used as a removal technology for VOCs.

본 연구는 스파티필름의 수분 스트레스 정도에 따라 실내 공간 내 오염물질 제거 효율을 구명하고자 수행하였다. 식물이 없는 공간을 대조구, 정상적인 스파티필름과 수분 스트레스를 받은 스파티필름을 각각의 처리구로 하였다. 스파티필름의 수분 스트레스 유무에 따른 chamber 내 온도를 조사한 결과 대조구와 처리구 모두 식물의 생육 적정 범위인 23±1℃를 유지하였으며, 처리 간의 0.7℃의 차이를 보였다. 습도의 경우 대조구와 처리구는 유의차 있게 나타났으며, 처리 간의 유의 차는 없는 것으로 나타났다. 수분 스트레스에 따른 실내 오염 물질을 조사한 결과, 포름알데히드(Formaldehyde) 경우 대조구는 0.30mg･m-3, 정상적인 스파티필름은 0.05mg･m-3 , 수분 스트레스를 받은 스파티필름은 0.09mg･m-3으로 대조구와 처리구는 통계적으로 유의차를 보였으며, 식물 내 수분 스트레스에 따른 처리구간에는 유의차가 없었다. TVOC(Total Volatile Organic Compound)조사 결과, 정상적인 스파티필름의 TVOC는 5시간 후 0.00mg･m-3 으로 모두 제거 된 반면, 수분 스트레스를 받은 스파티필름은 0.34mg･m-3으로 다소 남아 있었으며, 대조구는 1.25mg･m-3으로 세 처리 모두 통계적으로 유의차 있게 나타났다. 또한 이산화탄소 변화량 조사결과, 대조구는 459ppm, 정상 스파티필름은 446ppm으로 통계적으로 유의한 차이는 없으며, 수분 스트레스를 받은 스파티 필름이 대조구보다 이산화탄소 함량이 다소 높았다. 기공변화율 조사 결과, 정상 스파티필름의 변화율은 높게 나타났으며, 수분 스트레스를 받은 스파티필름은 변화율이 낮은 것으로 조사되었다. 따라서, 스파티필름이 배치되어있지 않은 공간보다 배치된 공간이 공기정화에 효과적이며, 수분 스트레스를 받은 스파티필름은 실내오염물질 제거에 있어서 기공 변화율 및 이산화탄소 흡수능력이 저하되므로 스파티필름을 이용하여 효과적으로 실내오염물질을 제거하기 위해서는 적절한 수분 관리가 필요한 것으로 판단된다.

A pilot-scale biocover was installed at a sanitary landfill for municipal waste, and the removal of volatile organic compounds (VOCs) by the biocover was evaluated for a long period of 550 days. The biocover (2.5 m W × 5 m L × 1 m H) was constructed with the mixture of soil, perlite, earthworm cast and compost (6:2:1:1, v/v). The total VOCs concentration of the inlet gas into the biocover was 820.3 ppb~7,217.9 ppb, and the total VOCs concentration of the outlet gas from the surface of the biocover was 12.6 ppb~1,270.1 ppb. The average removal efficiency of total VOCs was 87.6 ± 11.0% (60.5% for minimum and 98.5% for maximum). Toluene concentration was the highest among the inlet VOCs, followed by ethylbenzene, m, p-xylene and o-xylene. These aromatic VOCs accounted for more than 50% of the total VOCs concentration. Other than these aromatic VOCs, hexane, cyclohexane, heptane, benzene, and acetone were major VOCs among the inlet VOCs. Compared with the VOC profiles in the inlet gas, the relative contribution of dichloromethane to the outlet VOCs emitted from the biocover layer increased from 0.1% to 15.3%. The average removal efficiencies of BTEX in the biocover were over 84% during the operation period of 550 days. The average removal efficiencies of hexane, cyclohexane and heptane in the biocover were 86.0 ± 18.9%, 85.4 ± 20.4% and 97.1 ± 4.0%, respectively. The removal efficiency of VOCs in the biocover decreased not only when the ambient temperature had fallen below 5oC, but also when the ambient temperature had risen above 23oC. Information on the VOCs removal characteristics of the biocover installed in the landfill field can be useful for commercializing the biocover technology for the treatment of VOCs.

In this study, volatile organic compounds (VOCs) emitted from printing industries were analyzed, and an inorganic adsorbent, γ-alumina, was selected for the effective control of the VOC emissions. Printing processes commonly require inks, thinners, and cleaners, and they were mixed organic solvents containing aromatic compounds, ketones, and alcohols. Therefore, toluene, methyl ethyl ketone (MEK), and isopropyl alcohol (IPA) were selected as model compounds for this study. The adsorptive properties using γ-alumina were determined for the model compounds. Both batch isotherm and continuous flow column tests demonstrated that the adsorption capacity of MEK and IPA was 3~4 times higher than that of toluene. The column test performed at an inlet toluene concentration of 100 ppm showed that an 80% breakthrough for toluene was observed after 3 hours, but both MEK and IPA were continuously adsorbed during the same time period. A numerical model simulated that the γ-alumina could remove toluene at a loading rate of 0.4 mg/min only for a 4-hour period, which might be too short of a duration for real applications. Consequently, lifetime enhancement for γ-alumina must be implemented, and ozone oxidation and regeneration would be feasible options.

To abate the problem of odor from restaurants, a hybrid adsorbent consisting of organic and inorganic materials was developed and evaluated using acetaldehyde as a model compound was deveioped and evaluated. Powders of activated carbon, bentonite, and calcium hydroxide were mixed and calcinated to form adsorbent structure. The surface area of the hybrid adsorbent was smaller than that of high-quality activated carbon, but its microscopic image showed that contours and pores were developed on its surface. To determine its adsorption capacity, both batch isotherm and continuous flow column experiments were performed, and these results were compared with those using commercially available activated carbon. The isotherm tests showed that the hybrid adsorbent had a capacity 40 times higher than that of the activated carbon. In addition, the column experiments revealed that breakthrough time of the hybrid adsorbent was 2.5 times longer than that of the activated carbon. These experimental results were fitted to numerical simulations by using a homogeneous surface diffusion model (HSDM); the model estimated that the hybrid adsorbent might be able to remove acetaldehyde at a concentration of 40 ppm for a 5-month period. Since various odor compounds are commonly emitted as a mixture when meat is barbecued, it is necessary to conduct a series of experiments and HSDM simulations under various conditions to obtain design parameters for a full-scale device using the hybrid adsorbent.

본 실험에서는 실제 원수와 모사 원수를 이용하여 유기막(PES, PVDF 및 PTFE)을 이용하여 재질에 따른 막오염 특성을 분석하고자 하였다. 먼저 원수를 운전압력 1kgf/cm2로 여과하였다. 재질별 소요된 여과 시간은 약 5분, 약 13분, 약 17분으로 각각 나타났다. 또한 모사 원수 실험을 진행하였고, 원수 실험과 동일한 결과를 나타냈다. Jucker 와 Clark(1994)에 따르면 소수성 재질의 막이 유기물 흡착에 의한 Flux 감소가 크다고 보고하였고, 본 실험에서도 소수성 재질의 막이 높은 Flux 감소율을 나타났다. 실험 결과를 통해 막 재질 특성이 조류 유입에 따른 Flux 감소율에 영향을 미치는 것을 확인하였다. 본 연구는 환경부의 “환경정책기반공공기술개발사업”으로 지원받은 과제입니다.

Prussian blue is known as a superior material for selective adsorption of radioactive cesium ions; however, the separation of Prussian blue from aqueous suspension, due to particle size of around several tens of nanometers, is a hurdle that must be overcome. Therefore, this study aims to develop granule type adsorbent material containing Prussian blue in order to selectively adsorb and remove radioactive cesium in water. The surface of granular activated carbon was grafted using a covalent organic polymer (COP-19) in order to enhance Prussian blue immobilization. To maximize the degree of immobilization and minimize subsequent detachment of Prussian blue, several immobilization pathways were evaluated. As a result, the highest cesium adsorption performance was achieved when Prussian blue was synthesized in-situ without solid-liquid separation step during synthesis. The sample obtained under optimal conditions was further analyzed by scanning electron microscope-energy dispersive spectrometry, and it was confirmed that Prussian blue, which is about 9.7% of the total weight, was fixed on the surface of the activated carbon; this level of fixing represented a two-fold improvement compared to before COP-19 modification. In addition, an elution test was carried out to evaluate the stability of Prussian blue. Leaching of Prussian blue and cesium decreased by 1/2 and 1/3, respectively, compared to those levels before modification, showing increased stability due to COP-19 grafting. The Prussian blue based adsorbent material developed in this study is expected to be useful as a decontamination material to mitigate the release of radioactive materials.

대형저서동물에서 우점하고 있는 갯지렁이류는 퇴적층의 유기물 섭취를 통하여 저질환경개선 에 중요한 역할을 한다. 본 연구에서는 최근 양식기술이 개발된 바위털갯지렁이를 이용하여 갯 벌 퇴적층의 유기물 제거효과를 검토하였다. 이를 위하여 입자특성이 다른 세종류의 저질환경 (S1: 강사질, S2: 해사질, S3: 니사질)에서 해수 및 퇴적층의 TOC를 측정하였다. 바위털갯지렁이 는 세종류의 입자특성에서 모두 유기물 제거효과를 나타내었으며, 입자가 클수록 제거율이 높 았다. 유기물 정화능력을 정량적으로 평가한 결과 바위털갯지렁이는 각 저질별로 강사질에서 3.9856 ppm g-1d-1, 해사질에서 2.8021 ppm g-1d-1, 그리고 니사질에서 28.1142 ppm g-1d-1의 제거능력을 나타내었다. 본 연구결과는 바위털갯지렁이가 다양한 저질에서 유기물 제거에 기 여하고 있음을 보여 주었다.

It is necessary to develop a mobile water production system in order to provide stable water supply in case of disasters such as floods or earthquakes. In this study, we developed a modular mobile water production system capable of producing water for various uses such as domestic water and drinking water while improving applicability in various raw water sources. The water production system consists of three stages of filtration (sand filtration - activated carbon filtration - pressure filtration) to produce domestic water and an additional reverse osmosis process to produce drinking water. In laboratory and field experiments, the domestic water production system showed excellent treatment efficiency for particulate matter, but showed limitations in the treatment of dissolved substances such as dissolved organic matter. In addition, ultraviolet irradiation was considered as additional disinfection step, because it does not form precipitates of manganese oxides after disinfection. Reverse osmosis process was added to increase the removal efficiency of dissolved substances and the treated water satisfied drinking water quality standards. Fluorescence analysis of dissolved organic matter showed that the fulvic acid-like substances in raw water was successfully removed in the reverse osmosis process. The mobile water production system developed in this study is expected to be used not only in water supply in case of disaster, but also widely used in islands and rural area.

부영양화 호소수에 대한 국내 서식 펄조개(A. woodiana)의 유기물 제어 실험 결과, 펄조개 30개체를 대상으로 패각 크기 4.3~15.5 cm (평균 9.54 cm)에 따른 유기물 여과율은 0.08∼0.86L g-1 h-1, 단위 건중량당 펄조개의 여과율은 0.09L g-1 h-1를 나타내었다. 펄조개의 배설물 생산량 (PF)은 0.00∼11.10mg g-1 h-1, 단위 건 중량당 배설물 생산량은 0.37mg g-1 h-1를 나타내었다. 또한, 클로로필-a와 부유물질 제거율(RA, %)은 느린 유속에서 82.1%, 71.0% 빠른 유속에서는 65.4%, 57.5%의 제거율을 나타냈고, 반응표면분석 결과, 패각 크기는 14.3~15.6 cm, 유속은 22∼30Lh-1 구간에서 여과율 6.21L mussel-1 d-1의 최적값을 나타내었다. 또한, 배설물 생산능은 패각 크기는 14.3~16.3 cm, 유속은 36∼44Lh-1 구간에서 배설물 생산이 4.2mg g-1 d-1의 최적값을 나타내었다.

Ultrapure water (UPW) is water containing nothing but water molecule (H2O). The use of UPW is increasing in many industries such as the thermal and nuclear power plants, petrochemical plants, and semiconductor manufacturers. In order to produce UPW, several unit processes such as ion exchange, reverse osmosis (RO), ultraviolet (UV) oxidation should be efficiently arranged. In particular, RO process should remove not only ions but also low molecular weight (LMW) organic matters in UPW production system. But, the LMW organic matter removal data of RO membranes provided by manufacturers does not seem to be reasonable because they tested the removal in high concentration conditions like 1,000 ppm of isopropyl alcohol (IPA, MW=60.1). In this study, bench-scale experiments were carried out using 4-inches RO modules. IPA was used as a model LMW organic matter with low concentration conditions less than 1 ppm as total organic carbon (TOC). As a result, the IPA removal data by manufacturers turned out to be trustable because the effect of feed concentration on the IPA removal was negligble while the IPA removal efficiency became higher at higher permeate flux.

도시지역 합류식 하수배제 설비인 우수받이 및 하수관거, 정화조 등에는 유기성 고형 물이 퇴적되기 쉬우며, 유기성 퇴적물이 부패되는 과정에서 고농도의 황계열 악취물질이 발생한다. 본 연구에서는 전기산화방식을 이용하여 유기성 퇴적물 내에 용존된 악취물질 및 전구물질을 저감시켜, 하수관거에서 기상으로 배출되는 악취 문제를 해결하고자 하였다. 실험실 규모의 밀폐된 회분식 반응기에 하수슬러지(COD 기준 8,000 ~ 28,000 mg·L-1)를 투입하고, 발생되는 악취물질 농도와 악취발생특성을 조사하였다. 여기에 전기산화시스템 을 적용하여 황계열 악취물질과 전체 유기물의 산화 및 분해실험을 진행하였다. 전기산 화 실험을 진행한 결과, 밀폐된 반응기의 기상에서 450 ppm의 고농도로 발생한 황화수 소가 반응 30분 이내에 검출한계 이하까지 제거되었으며, 메틸머켑탄과 디메틸설파이드 는 85% 이상 제거되었다. 투입된 전기에너지당 황계열 악취물질의 제거율은 최대 0.33 mg-S·kJ-1로 나타났다. 또한 1시간의 반응기간 동안 회분식 반응기 내에서 황계열 악취물 질 뿐만 아니라 고농도 퇴적물에 함유된 전체 유기물 농도가 56% 감소하여, 전기산화시 스템이 악취를 유발하는 유기성 전구물질을 동시에 저감하는 효과를 나타내었다. 결과적 으로 최소한의 전기에너지를 이용하여 하수관거 퇴적 유기물에 의한 악취문제를 해결할 수 있을 것으로 기대된다