• 제목/요약/키워드: Adsorption/Removal

검색결과 1,335건 처리시간 0.029초

광산산성폐수에 함유된 중금속 처리를 위한 Chemical Fixation과 Bentonite의 흡착 (Chemical Fixation and Sorption of Bentonite for the Removal of Heavy Metals in Acid Mine Drainage (AMD))

  • 장암;김인수
    • 한국토양환경학회지
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    • 제5권2호
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    • pp.33-43
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    • 2000
  • 적절한 조치 없이 방치되어온 폐광재가 폐광산 근교 및 멀리 떨어진 지역의 유휴지 혹은 농경지까지 다양한 경로를 통해 영향을 주고 있다. 중금속은 일반적인 방법으로 더 이상 분해되지 않는 원소 상태로 존재하고, 단순 매립할 경우 처분후에도 계속적인 용출과정이 일어날 수 있으므로 물리 화학적으로 보다 안정된 상태로 고정화시켜야 한다. 본 연구에서 화학적 고정화 첨가제로 사용된 CaO, $Na_2$Sㆍ$5H_2$O, $CaCO_3$순으로 각 중금속에 대해 높은 고정화 Capacity (q)와 효율 (k)을 나타냈으며 bentonite가 다른 토양보다 물리 화학적 특성과 고정화능이 우수하여 이들이 ADM를 고정화하는 좋은 첨가제라고 사료된다. bentonite 50g에 흡착된 각 중금속에 대하여 Freundlich 등온식을 적용해서 Freundlich등온식의 상수인 n과 k값을 나타내었다.

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악취물질인 유기산 제거를 위한 DBD 플라즈마 촉매 복합공정의 적용 (Application of DBD Plasma Catalysis Hybrid Process to remove Organic Acids in Odors)

  • 홍은기;서정민;최금찬
    • 한국환경과학회지
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    • 제23권9호
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    • pp.1627-1634
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    • 2014
  • Odor control technology include absorption, adsorption, incineration and biological treatments. But, most of processes have some problems such as secondary organic acids discharge at the final odor treatment facility. In order to solve the problems for effective treatment of organic acids in odor, it is necessary to develop a new type advanced odor control technology. Some of the technology are plasma only process and plasma hybrid process as key process of the advanced technology. In this study, odor removal performance was compared DBD(Dielectric Barrier Discharge)plasma process with PCHP(plasma catalysis hybrid process) by gaseous ammonia, formaldehyde and acetic acid. Plasma only process by acetic acid obtained higher treatment efficiency above 90%, and PCHP reached its efficiency up to 96%. Acetic acid is relatively easy pollutant to control its concentration other than sulfur and nitrogen odor compounds, because it has tendency to react with water quickly. To test of the performance of DBD plasma process by applied voltage, the tests were conducted to find the dependence of experimental conditions of the applied voltage at 13 kV and 15 kV separately. With an applied voltage at 15 kV, the treatment efficiency was achieved to more higher than 13 kV from 83% to 99% on ammonia, formaldehyde and acetic acid. It seems to the odor treatment efficiency depends on the applied voltage, temperature, humidity and chemical bonding of odors.

고수부지활용 수질정화 자유수면 인공습지의 초기처리수준 (Treatment Efficiency of a Surface - Flow Wetland System Constructed on Floodplain)

  • 양홍모
    • 한국환경농학회지
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    • 제20권4호
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    • pp.277-283
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    • 2001
  • This paper presents treatment efficiency and plant growth of a surface-flow constructed wetland system (30 meter in length and 10 meter in width) over one year after its establishment on a floodplain of a stream. Cattails (Typha angustiflora) grown on pots were transplanted on one half of its area from inlets and reeds (Phragmites australis) on another half from an outlet. Effluent discharged from a secondary-level treatment plant was funneled into the system. The stems of cattails and reeds emerging in April 2001 grew up to 165.9 cm and 95.3 cm, respectively until July 2001. The number of stems of cattails arid reeds in July 2001 increased by 65% and 100%, respectively, compared with that just after their planting. The growth of cattails was better than that of reeds during study period. The removal rates for SS, $BOD_5$, T-N and T-P was 33%, 43%, 31%, and 51%, respectively. The system was inundated seven times by storms over the monitoring period, which disturbed its environment and led to its lower treatment rates. The increase of SS concentration in effluent after inundation of the system was attributed to the falls of soil particles onto its water surface, which had been attached to the emergent plants by floods. Purification rates for T-N were relatively low for the period of late fall through winter until early spring due to lower water temperature which may have retarded microbial nitrification and denitrification mechanisms. Reduction in T-P concentration during fall and winter was relatively higher than that during summer and spring, which may have resulted from no system perturbations by floods and heavy storms during fall and winter.

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염산 및 불산처리 모더나이트의 산특성과 촉매활성 (Acid Property and Catalytic Activity on Mordenites Treated by Hydrochloric Acid and Hydrofluoric Acid)

  • 한영택;하백현
    • 공업화학
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    • 제2권1호
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    • pp.77-85
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    • 1991
  • 염산 및 불산으로 모더나이트를 처리하여 실리카/알루미나 비가 다른 일련의 시료를 만들었다. 이러한 시료에 대하여 암모니아 TPD와 피리딘 흡착으로 IR을 이용하여 산성도를 측정하고 o-xylene 반응의 활성과 이성화반응에 대한 선택성을 측정하였다. 그 결과 염산처리 시료는 실리카/알루미나 비가 증가할수록 구조알루미늄이 추출되어 산량이 감소하였으며 실리카/알루미나 비가 22인 시료가 다른 시료들보다 활성이 좋았다. 불산처리 시료는 불산처리 시 불소가 구조 중 규소원자와 결합하였으며 처리시간이 증가함에 따라 결합된 불소는 증가하였다. 이 경우의 활성은 염산처리와는 달리 알루미늄의 추출과 함께 모더나이트의 수산기가 불소로 치환되어 이로 인하여 산점이 줄어 활성이 감소하나 불산은 규소도 추출하므로 표면을 파고들어 새로운 면이 노출되어 산점이 형성되고 이 산점은 증가된 결합불소의 영향을 받아 강해지면서 활성이 다소 증가하였다.

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트리페닐메탄계와 아조계 색소를 탈색할 수 있는 Klebsiella pneumoniae WL-5의 분리 및 특성 (Isolation and Characterization of Klebsiella pneumoniae WL-5 Capable of Decolorizing Triphenylmethane and Azo Dyes)

  • 우징;이영춘
    • 생명과학회지
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    • 제18권10호
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    • pp.1331-1335
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    • 2008
  • 여러 가지 난분해성 색소에 대하여 탈색능을 나타내는 Klebsiella pneumoniae WL-5이 염색폐수처리장의 활성슬러지로부터 분리되었다. 이 세균은 정치배양과 at pH 6-8 및 $30-35^{\circ}C$에서 높은 탈색능을 나타내었다. Congo Red색소에 대해서는 $200\;{\mu}M$ 농도에서 12시간 배양하였을 때 90% 이상이 탈색되었고, Malachite Green, Brilliant Green, Reactive Black-5에 대해서는 $10\;{\mu}M$ 농도에서 80% 이상이 탈색되었지만, Reactive Red-120, Reactive Orange-16, Crystal Violet에 대해서는 $10\;{\mu}M$ 농도에서 각각 46%, 25%, 13%의 비교적 낮은 탈색능을 나타내었다. 트리페닐메탄계 색소는 세포표면에의 흡착에 의한 탈색을 나타내었고, 아조계 색소는 지금까지 알려져 있지 않는 새로운 효소반응계에 의해서 탈색된다는 것을 제시하였다.

One-pot 합성 방법을 이용한 나노 철입자가 담지된 폐목재 기반 하이드로차의 제조 및 특성 평가 (Preparation of Iron Nanoparticles Impregnated Hydrochar from Lignocellulosic Waste using One-pot Synthetic Method and Its Characteristics)

  • 최유림;김동수;;안혜영;박광진;양재규;장윤영
    • 한국지하수토양환경학회지:지하수토양환경
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    • 제25권1호
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    • pp.95-105
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    • 2020
  • In this study, iron nanoparticles impregnated hydrochar (FeNPs@HC) was synthesized using lignocellulosic waste and simple one-pot synthetic method. During hydrothermal carbonization (HTC) process, the mixture of lignocellulosic waste and ferric nitrate (0.1~0.5 M) as a precursor of iron nanoparticles was added and heated to 220℃ for 3 h in a teflon sealed autoclave, followed by calcination at 600℃ in N2 atmosphere for 1 h. For the characterization of the as-prepared materials, X-ray diffraction (XRD), cation exchange capacity (CEC), fourier transform infrared spectrometer (FT-IR), Brunauer-Emmett-Teller (BET), transmission electron microscope (TEM), Energy Dispersive X-ray Spectroscopy (EDS) were used. The change of Fe(III) concentration in the feedstock influenced characteristics of produced FeNPs@HC and removal efficiency towards As(V) and Pb(II). According to the Langmuir isotherm test, maximum As(V) and Pb(II) adsorption capacity of Fe0.25NPs@HC were found to be 11.81 and 116.28 mg/g respectively. The results of this study suggest that FeNPs@HC can be potentially used as an adsorbent or soil amendment for remediation of groundwater or soil contaminated with arsenic and cation heavy metals.

소성된 Mg-Al Layered Double Hydroxide에 의한 비소(V)의 흡착 (Sorption of Arsenate by the Calcined Mg-Al Layered Double Hydroxide)

  • 서영진;강윤주;최정;김준형;박만
    • 한국토양비료학회지
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    • 제41권6호
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    • pp.369-373
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    • 2008
  • Mg-Al LDH를 이용하여 수용액중 비소와의 반응특성을 규명하고 비소 제거제로서 활용가능성을 규명하기 위하여 비소의 흡착특성, 제거효율 및 제거기작에 대한 조사를 하였다. Mg-Al LDH는 소성(calcination)에 의한 탈수로 Mg oxide 형태를 나타내었고 비소를 흡착시킨 결과 반응 22시간 이후에 흡착평형에 도달하였으며 흡착량은 약 530 mmol/kg정도였다. 반응농도별 LDH의 등온흡착은 L-type의 흡착반응을 나타내었다. 소성된 Mg-Al LDH는 용액중에서 재수화(rehydration) 될 때 비소가 LDH의 구조의 복구과정(reconstruction)에서 이온교환 반응에 의해 층간삽입이 일어나는 것으로 나타났다. LDH에 대한 arsenate와 phosphate, arsenate와 sulfate의 경쟁흡착 결과 arsenate와 phosphate의 선택성은 비슷한 편이었고, arsenate는 sulfate에 비해 선택성이 우수하였다. 따라서 calcined Mg-Al LDH는 비교적 높은 비소 제거효율을 나타내므로 비소 제거제로서 사용 가능성이 매우 높은 것으로 판단된다.

광촉매(光觸媒) 산화(酸化) 반응(反應)을 이용한 클로로페놀 분해(分解)에 관한 연구(硏究) (A Study on the Removal of Chloro-Phenols by Photocatalytic Oxidation)

  • 이상협;박주석;박중현
    • 상하수도학회지
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    • 제9권4호
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    • pp.87-96
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    • 1995
  • The Electron/Hole Pair is generated when the activation energy produced by ultraviolet ray illuminates to the semiconductor and OH- ion produced by water photocleavage reacts with positive Hole. As a results, OH radical acting as strong oxidant is generated and then Photocatalytic oxidation reaction occurs. The photocatalytic oxidation can oxidate the non-degradable and hazardous organic substances such as pesticides and aromatic materials easier, safer and shorter than conventional water treatment process. So in this study, many factors influencing the oxidation of chlorophenols, such as inorganic electrolytes addition, change of oxygen and nitrogen atmosphere, temperature, pH, oxygen concentration, chlorophenol concentration, were throughly examined. According to the experiments observations, it is founded that the rate of chlorophenol oxidation follows a first-order reaction and the modified Langmuir-Hinshelwood relationship. And the photocatalytic oxidation occurs only when activation energy acting as Electron/Hole generation, oxygen acting as electron acceptor to prevent Electron/Hole recombination, $TiO_2$ powder acting as photocatalyst are present. The effects of variation of dissolved oxygen concentration, temperature and inorganic electrolytes concentration on 2-chlorophenol oxidation are negligible. And the lower the organic concentration, the higher the oxidation efficiency becomes. Therefore, the photocatalytic oxidation is much effective to oxidation of hazardous substances at very low concentration. The oxidation is effective in the range of 0.1 g/L-10 g/L of $TiO_2$. Finally when the ultra-violet ray is illuminated to $TiO_2$, the surface characteristics of $TiO_2$ change and Adsorption/Desorption reaction on $TiO_2$ surface occurs.

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Thermo-responsive antifouling study of commercial PolyCera® membranes for POME treatment

  • Haan, Teow Yeit;Chean, Loh Wei;Mohammad, Abdul Wahab
    • Membrane and Water Treatment
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    • 제11권2호
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    • pp.97-109
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    • 2020
  • Membrane fouling is the main drawback of membrane technology. Frequent membrane cleaning and membrane replacement are, therefore, required to reduce membrane fouling that causes permeate flux reduction, lower rejection, or higher operating pressure. Studies have proved that the alteration of membrane properties is the key controlling factor in lessening membrane fouling. Among stimuli-responsive membranes, thermo-responsive membrane is the most popular, with a drastic phase transition and swelling-shrinking behavior caused by the temperature change. In this study, the thermo-responsive ability of two commercial membranes, PolyCera® Titan membrane and PolyCera® Hydro membrane, at different temperatures was studied on the antifouling function of the membrane in palm oil mill effluent (POME) treatment. The evaluation of the membrane's thermo-responsive ability was done through three cycles of adsorption (fouling) and desorption (defouling) processes in a membrane filtration process. The experimental result depicted that PolyCera® Hydro membrane had a higher membrane permeability of 67.869 L/㎡.h.bar than PolyCera® Titan membrane at 46.011 L/㎡.h.bar. However, the high membrane permeability of PolyCera® Hydro membrane was compensated with low removal efficiency. PolyCera® Titan membrane with a smaller mean pore size had better rejection performance than PolyCera® Hydro membrane for all tested parameters. On the other hand, PolyCera® Titan membrane had a better hydrodynamic cleaning efficiency than PolyCera® Hydro membrane regardless of the hydrodynamic cleaning temperature. The best hydrodynamic cleaning performed by PolyCera® Titan membrane was at 35℃ with the flux recovery ratio (FRR) of 99.17 ± 1.43%. The excellent thermo-responsive properties of the PolyCera® Titan membrane could eventually reduce the frequency of membrane replacement and lessen the use of chemicals for membrane cleaning. This outstanding exploration helps to provide a solution to the chemical industry and membrane technology bottleneck, which is the membrane fouling, thus reducing the operating cost incurred by the membrane fouling.

아민화 GMA-DVB 공중합체의 합성과 질소 성분에 대한 흡착 특성 (Synthesis of Aminated GMA-DVB Copolymer and Their Adsorption Properties for Nitrate)

  • 황택성;이선아;이면주
    • 폴리머
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    • 제25권3호
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    • pp.311-317
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    • 2001
  • 본 연구에서는 반응성이 큰 친수성 단량체인 glycidylmethacrylate (GMA)를 이용하여 현탁중합법으로 bead type의 GMA-DVB 공중합체를 제조하고, 이들 공중합체를 trimethyl-ammonium chloride로 아민화하여 trimethylammonium기를 갖는 거대망상형 음이온 교환수지를 합성하였다. 여기서 지하수에 공존하는 음이온 중 $NO_3^-$ 제거에 가장 방해가 되는 $SO_4^{2-}$ 이 입체적으로 크다는 것에 착안하여 가교제인 divinylbenzene (DVB)의 양을 변화시켜 가교도에 따른 음이온에 대한 선택능을 확인하였고, 각각의 수지에 대한 물성과 $NO_3^-$ 에 대한 흡착능을 고찰하였다. 또한 FT-IR을 통하여 공중합체의 합성여부를 확인하였고, 또한 아민화 수율, 이온교환 용량 및 팽윤율을 평가하여 가교도에 따른 영향을 조사하였다. 여기서 DVB의 함량이 4wt%일 때 아민화 수율은 384.3%, 이온교환용량은 3.25 meq/g, 팽윤율은 77.1%로 가장 최적으로 나타났다.

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