• Advances in environmental research
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• 제2권4호
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• pp.309-321
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• 2013

High AA new high capacity sorbent for preconcentration and determination of nickel in environmental samples was synthesized. The sorbent was synthesized by copolymerization of allyl glaycidyl ether / imminodiacetic acid with N,N-dimethylacrylamide as functional monomers in the presence of N,N-bismethylenacryl amid as cross linker and characterized by Fourier transform infra red spectroscopy, elemental analysis, thermogravimetric analysis and scanning electron microscopy. A recovery of 93.6% was obtained for the metal ion with 0.1 M, sulfuric acid as the eluting agent. The sorption capacity of the functionalized sorbent was 55.9 $mgg^{-1}$. The equilibrium sorption data of Ni(II) on polymeric sorbent were analyzed using Langmuir, Freundlich, Temkin and Redlich.Peterson models. Based on equilibrium adsorption data the Langmuir, Freundlich and Temkin constants were determined 0.87 (L mg-1), 25.87 ($mgg^{-1}$) $(Lmg^{-1})^{1/n}$ and 171.4 ($Jmol^{-1}$) respectively at pH 4.5 and $20^{\circ}C$.

• Journal of Radiation Protection and Research
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• 제17권2호
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• pp.49-59
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• 1992

이온 또는 착화된 상태의 방사성핵종의 이동에 대한 착화제의 영향을 조사하기 위하여 새로운 모델이 제시되었다. 착화된 방사성핵종의 이동거동은 착화제와 착화된 방사성핵종의 열화를 포함하는 대류-확산 이동방정식에 의해 해석되었다. 이 수학적 모델은 해석적인 방법 에 의해 구해졌으며 지연요소를 조사함으로써 분석되었다. 계산결과들은 감소된 지연요소에 의해 착화된 방사성핵종의 이동속도가 이온형태의 방사성핵종보다 매우 빠름을 보여주었다. 따라서 원자력발전소로부터의 착화제의 발생과 환경으로의 유출을 감소시킬 수 있는 새로운 구제책이 필요하다고 하겠다.

• 한국철도학회:학술대회논문집
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• 한국철도학회 2006년도 추계학술대회 논문집
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• pp.1385-1390
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• 2006

Concrete structure can be deteriorated by ingress of moisture and aggressive agents. To maintain the sound performance of concrete structure during the service life, it needs to protect concrete from ingress of moisture and aggressive agents before arising deterioration of concrete. Protection of concrete is possible by surface treatment. In this study, durability of the functional nano composite inorganic activated carbon based coatings which can provide a barrier against the ingress of moisture or aggressive ions to concrete is discussed. For the durability evaluation of the coatings, fine void structure evaluation test, chloride penetration acceleration test, accelerated carbonation test, freezing and thawing test, and the accelerated test of chemical erosion are conducted. As the result of this study, the functional nano composite inorganic activated carbon based coatings which became one formed complex compound with adsorption and porosity on concrete surface, had an effect on the function of far infrared radiation, antimicrobial action, air cleaning, airing assurance, and the interception of moisture of deterioration factor, chloride ion, carbon dioxide, sulfate, and so on.

• 한국미생물·생명공학회지
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• 제18권4호
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• pp.338-343
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• 1990

Streptomyces sp. DMCJ-49 균주의 배양액으로부터 분리된 $\alpha$-amylase 저해물질 MB4-03은 구조상 질소원자와 methyl기를 포함하는 일종의 직선형 Alpha(1-4) 결합으로 연결된 glucose의 변형된 oligomer 형태로서 구성 단당류는 12 정도로 추정된다.

• Bulletin of the Korean Chemical Society
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• 제5권3호
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• pp.108-112
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• 1984

Interactions between metal ions and chitosan in solution were studied by spectroscopic and viscometric measurements. $Cu^{++}$-chitosan complex exhibited an absorption band at 265 nm, whereas D-glucosamine complex showed one at 245 nm. The difference in ${\lambda}_{max}$ was attributed to the different amine to $Cu^{2+}$ ratios of the complexes, that is, 2 : 1 for chitosan and 1 : 1 for D-glucosamine. The molar absorptivities and binding constants of the complexes were evaluatatled. The binding of $Cu^{2+}$ to chitosan was cooperative near pH 5, and both intra- and intermolecular chelations depending on chitosan and $Cu^{2+}$concentrations were observed, The intermolecular chelation was stabilized by addition of salts. The cooperative intermolecular chelation of $Ni^{++}$ was also observed at pH 6.2. No significant binding of other divalent ions was observed. The reported high adsorption abilities of chitosan particles for these ions were attributed to the deposition of metal hydroxide aggregates in pores of chitosan particles rather than chelation to amine groups.

• 한국환경과학회지
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• 제27권11호
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• pp.975-982
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• 2018

In this study, zeolite (Z-C1) was synthesized using a fusion/hydrothermal method from coal fly ash. The morphological structures of Z-C1 were confirmed to be highly crystalline with a cubic crystal structure. Exchange capacities of $Ca^{2+}$ and $Mg^{2+}$ ions in a single and a mixed solution reached equilibrium within 120 min. The exchange kinetics of these ions were well predicted by the pseudo-second-order rate equation. The exchange isotherms of the $Ca^{2+}$ and $Mg^{2+}$ ions matched the Langmuir isotherm better than the Freundlich isotherm. The maximum cation exchange capacities ($q_m$) obtained by the Langmuir isotherm model were 2.11 mmol/g (84.52 mg/L) and 1.13 mmol/g (27.39 mg/L) for the $Ca^{2+}$ and $Mg^{2+}$ ions, respectively.

• Bulletin of the Korean Chemical Society
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• 제20권3호
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• pp.285-290
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• 1999

In the present paper, we report a molecular dynamics (MD) simulation study for the structure and dynamics of H+ ions in non-rigid dehydrated H12-A zeolite framework at 298.15 K, using the same method we used in our previous studies of rigid and non-rigid zeolite-A frameworks. It is found that two different structures appear, depending on the choice of the Lennard-Jones parameter (σ) for the H+ ion, as is also observed in the study of rigid dehydrated H12-A zeolite framework, but the ranges of σ are different for the two structures. It is also found that some of the H+ ions exchanged their sites without changing the number of H+ ions at each site. The agreement between experimental and calculated structural parameters for non-rigid dehydrated H12-A zeolite is generally quite good. The calculated IR spectrum by Fourier transform of the total dipole moment auto-correlation function shows two major peaks, one around 2700 cm-1 and the other around 7000 cm-1. The former appears in the calculated IR spectra of non-rigid zeolite-A framework only system and the latter remains unexplained except, perhaps, as an indication of a new formation of a vibrational mode of the framework due to the adsorption of the H+ ions.

• 대한금속재료학회지
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• 제49권5호
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• pp.400-405
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• 2011

ZnO nanotube arrays were synthesized by a two-step process: electrodeposition and selective dissolution. In the first step, ZnO nanorod arrays were grown on an Au/Si substrate by using a homemade electrodeposition system. ZnO nanorod arrays were then selectively dissolved in an etching solution composed of 0.125 M NaOH, resulting in hollow ZnO nanotube arrays. It is suggested that the formation mechanism of the ZnO nanotube arrays might be attributed to the preferred surface adsorption of hydroxide ion ($OH^{-1}$) on a positive polar surface followed by selective dissolution of the metastable Zn-terminated ZnO (0001) polar surface caused by the difference in the surface energy per unit area between the ZnO nanorod and nanotube.

• Corrosion Science and Technology
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• 제19권6호
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• pp.281-287
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• 2020

Chloride ion is one of the most important corrosive agents in atmospheric corrosion, especially in marine environments. It has high adsorption rate and increases the conductivity of electrolytes. Since chloride ions affect the protective properties and the surface composition of the corrosion product, they increase the corrosion rate. A low level of chloride ions leads to uniform corrosion, whereas a high level of chloride ions may induce localized corrosion. However, higher solution temperatures tend to increase the corrosion rate by enhancing the migration of oxygen in the solution. This work focused on the effect of NaCl concentration and temperature on galvanic corrosion between A516Gr.55 carbon steel and AA7075T6 aluminum alloys. When AA7075T6 aluminum alloy was galvanically coupled to A516Gr.55 carbon steel, AA7075T6 was severely corroded regardless of NaCl concentration and solution temperature, unlike the corrosion properties of single specimen. The combined effect of surface treatment involving carbon steel and aluminum alloy on corrosion behavior was also discussed.

• 한국토양비료학회지
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• 제40권4호
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• pp.311-325
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• 2007

오늘날 중금속으로 오염된 토양의 위해도 평가 및 오염토양 복원을 위한 기술의 적용에 있어서 점차 중금속의 생물유효도(bioavailability)가 총함량보다 중요하게 생각되고 있다. 그 결과 많은 연구자들은 토양과 토양수 내의 생물에 유효한 중금속의 함량을 조사함과 더불어 이 유효도에 영향을 미치는 주요 토양환경인자를 연구하고 있다. 따라서 본 총설은 일반적으로 유효도 평가에 이용되는 기존의 여러 방법들을 비교평가하고 중금속 유효도의 중요성을 이에 영향을 미치는 토양 인자와 함께기술하였다. 현재까지 다양한 유효도 측정 방법이 개발되어 많은 연구에 적용되고 있는데, 이에는 화학적 침출 방법 (chemical based extraction)과 이온 선택성 전극 (ion selective electrode, ISE) 및 확산구배막(diffusive gradient in the thin film, DGT)을 이용한 중금속 화학종 분리방법 등을 들 수 있다. 그러나 이와 같이 개발된 다양한 기술이 유효도 측정에 있어서 괄목할 만한 성과를 내고 있음에도 아직 국제적으로 인증되고 있는 기술이 있는 것은 아니다. 게다가 토양 중 중금속의 유효도는 토양의 종류 및 특성 그리고 측정 대상인 중금속의 종류에 따라 매우 다양한 양상을 보여준다. 토양 중 중금속의 유효도 변화는 주로 토양과 토양수 사이에서 일어나는 이온교환 반응을 통한 중금속 흡착(adsorption)과 탈착(desorption)에 의하여 일어나며 이 반응은 토양 pH, 유기물, 토양수 중 유기탄소(dissolved organic carbon, DOC), 유기산(low-molecular weight organic acids, LMWOAs) 및 주요 양이온과 같은 토양환경인자의 변화에 영향을 받는다. 예를들어 토양 pH의 증가는 탈수소화(deprotonation) 작용을 통해서 토양표면의 중금속 흡착능력을 높여 결과적으로 유효도를 감소시킨다. 토양중 유기물은 중금속 유효도를 감소시킴과 동시에 유기탄소 및 유기산의 원천으로서 유효도를 증가시키기도 한다. 즉, 유기물은 주로 음으로 하전된 표면을 가지고 있어 중금속을 고상으로 흡착시켜 유효도를 감소시킨다. 반면에 유기물에서 녹아 나온 토양수중 유기탄소 및 유기산은 강한 킬레이트(chelate)로서 토양표면으로부터 중금속을 떨어져 나오게 하여 유효한 중금속 함량을 높여준다. 이와 같은 중금속 이온과 토양인자 사이의 상호반응은 토양의 종류 및 중금속의 종류에 따라 매우 다양하다.