• 한국재료학회지
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• 제26권6호
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• pp.298-305
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• 2016

In this work, recent progress on graphene/metal oxide composites as advanced materials for $HgCl_2$ and $CO_2$ capture was investigated. Density Functional Theory calculations were used to understand the effects of temperature on the adsorption ability of $HgCl_2$ and water vapor on $CO_2$ adsorption on CaO (001) with reinforced carbon-based nanostructures using B3LYP functional. Understanding the mechanism by which mercury and $CO_2$ adsorb on graphene/CaO (g-CaO) is crucial to the design and fabrication of effective capture technologies. The results obtained from the optimized geometries and frequencies of the proposed cluster site structures predicted that with respect to molecular binding the system possesses unusually large $HgCl_2$ ($0.1-0.4HgCl_2g/g$ sorbent) and $CO_2$ ($0.2-0.6CO_2g/g$ sorbent) uptake capacities. The $HgCl_2$ and $CO_2$ were found to be stable on the surface as a result of the topology and a strong interaction with the g-CaO system; these results strongly suggest the potential of CaO-doped carbon materials for $HgCl_2$ and $CO_2$ capture applications, the functional gives reliable answers compared to available experimental data.

• Nuclear Engineering and Technology
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• 제52권2호
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• pp.328-336
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• 2020

Cesium is a major product of uranium fission, which is the most commonly existed radionuclide in radioactive wastes. Various technologies have been applied to separate radioactive cesium from radioactive wastes, such as chemical precipitation, solvent extraction, membrane separation and adsorption. Crown ethers and calixarenes derivatives can selectively coordinate with cesium ions by ion-dipole interaction or cation-π interaction, which are promising extractants for cesium ions due to their promising coordinating structure. This review systematically summarized and analyzed the recent advances in the crown ethers and calixarenes derivatives for cesium separation, especially focusing on the adsorbents based on extractants for cesium removal from aqueous solution, such as the grafting coordinating groups (e.g. crown ether and calixarenes) and coordinating polymers (e.g. MOFs) due to their unique coordination ability and selectivity for cesium ions. These adsorbents combined the advantages of extraction and adsorption methods and showed high adsorption capacity for cesium ions, which are promising for cesium separation The key restraints for cesium separation, as well as the newest progress of the adsorbents for cesium separation were also discussed. Finally, some concluding remarks and suggestions for future researches were proposed.

• 대한화학회지
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• 제54권5호
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• pp.533-540
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• 2010

활성탄소를 가지고 수용액으로부터 전이금속이온을 제거 능력에 대해 시험했다. 탄소의 물리적, 화학적 그리고 액체-상 흡착 특징은 다음의 기준 절차로 수행하였다. Ni(II), Cu(II) 그리고 Fe(III)이온의 제거 연구는 흡착물질의 양, 금속이온 용액의 pH, 배치 모드에서 시간을 다양하게 하여 시도되었다. 평균 흡착 데이터는 Freundlich와 Langmuir로 맞춰졌고 등온 상수는 계산되었다. 다른 세가지 금속 이온의 평균 시간은 결정되었다. pH는 흡착에 있어서 중요한 역할을 하는 것을 발견했다. 이 과정은 흡열반응이었고, 열역학 인자는 계산되었다. 흡착 연구는 이온교환 메커니즘이 작용되는 것을 나타내고 있다.

• Journal of Electrochemical Science and Technology
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• 제10권1호
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• pp.69-81
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• 2019

The corrosion inhibiting mechanism of Vietnam orange peel essential oil (OPEO) for mild steel in 1 N HCl solution was investigated elaborately. Corrosion inhibition ability of OPEO was characterized by electrochemical polarization, electrochemical impedance spectroscopy (EIS), and weight loss method. In the corrosive solution, OPEO worked as a mixed inhibitor and the inhibition efficiency of OPEO increased with the increase of its concentration. High inhibition efficiencies over 90% were achieved for the concentration of 3 - 4 g/L OPEO, comparable to that of 3.5 g/L urotropine (URO), a commercial corrosion inhibitor for acid media used in industry. By using adsorption isotherm models (Langmuir, Temkin and Frumkin), thermodynamic parameters of adsorption were calculated. The obtained results indicated physical adsorption mechanism of OPEO on the steel surface. The components responsible for the corrosion inhibition activity of OPEO were not only D-limonene, but also other compounds, which contain C=O, C=C, O-H, C-O-C, -C=CH and C-H bonding groups in the molecules.

• 공업화학
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• 제33권2호
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• pp.133-144
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• 2022

Fast-paced industrial and agricultural development generates large quantities of hazardous heavy metals (HMs), which are extremely damaging to individuals and the environment. Research in both academia and industry has been spurred by the need for HMs to be removed from water bodies. Advanced materials are being developed to replace existing water purification technologies or to introduce cutting-edge solutions that solve challenges such as cost efficacy, easy production, diverse metal removal, and regenerability. Water treatment industries are increasingly interested in activated carbon because of its high adsorption capacity for HMs adsorption. Furthermore, because of its huge surface area, abundant functional groups on surface, and optimal pore diameter, the modified activated carbon has the potential to be used as an efficient adsorbent. Metal-organic frameworks (MOFs), a novel organic-inorganic hybrid porous materials, sparked an interest in the elimination of HMs via adsorption. This is due to the their highly porous nature, large surface area, abundance of exposed adsorptive sites, and post-synthetic modification (PSM) ability. This review introduces PSM methods for MOFs, chemical modification of activated carbons (ACs), and current advancements in the elimination of Pb²⁺, Hg²⁺, and Cd²⁺ ions from water using modified MOFs and ACs via adsorption.

• 한국수산과학회지
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• 제34권5호
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• pp.473-477
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• 2001

Chitosan의 탈아세틸화도와 분자량 등을 달리하여 chitosan의 제조조건에 따른 수용성 단백질에 대한 흡착율 및 흡착에 영향을 미치는 인자에 대해 검토하였다. Chitosan의 탈아세틸화 조건을 $60\%,\;70\%,\;80\%$로 달리 하여 albumin, hemoglobin, albumin-myoglobin 혼합용액에 적용했을 때 chitosan의 탈아세틸화도가 높을 수록 chitosan과 수용성 단백질 사이의 흡착율은 높게 나타났다. 초음파 처리에 의하여 chitosan의 분자량을 변화시켰을 때 chitosan의 분자량이 작을수록 chitosan과 수용성 단백질 사이의 홉착율은 높게 나타났다 pH 변화에 따른 chitosan과 수용성 단백질의 흡착율은 albumin 및 albumin-myoglobin 혼합용액에서는 pH 4에서, hemoglobin 용액에서는 pH 7에서 홉착율이 높게 나타났다. Chitosan과 수용성단백질과의 흡착에서 반응시간은 albumin 및 albumin-myoglobin 혼합용액에서는 4시간, hemoglobin 용액에서는 3시간까지 흡착을이 증가하였고, 그 이상의 시간을 반응시켜도 흡착율의 증가는 거의 나타나지 않았다. 수용성 단백질 용액에 NaCl 농도를 0.1에서 1.0M로 증가시켜 첨가했을 때 염의 농도가 높을수록 chitosan과 수용성 단백질 사이의 흡착이 잘 일어나지 않았다.

• 한국토양환경학회지
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• 제1권1호
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• pp.11-17
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• 1996

본 실험은 산업 현장에서 광범위하게 사용하고 있는 유기용제인 Trichloroethylene (TCE)이 저장탱크누출, 작업장에서의 취급 부주의, 매립지 침출수 유출 등을 통해 토양과 지하수를 오염시킬 우려가 있는 물질이므로 토양내에서의 TCE의 흡착성향을 파악하기 위하여 본 연구를 수행하였다. 이를위해 토양의 유기물 함량과 석회 시용량을 달리하여 TCE에 대한 Freundlich 등온흡착식 상수 k와 n을 결정하였다. 유기물함량은 sewage sludge cake을 0ton/ha, 50ton/ha, 100ton/ha 수준으로 처리하고 S1, S2, S3라 명명하였다. 석회는 2ton/ha, 4ton/ha, 6ton/ha, 10ton/ha. 수준으로 처리하였다. sewage sludge cake을 수준별로 처리한 실험에서 구한 Freundlich 등온흡착식은 다음과 같다. (단, TCE 처리 농도범위가 0.5~2.5ng/g soil 일 경우임) S1 : x/m = 0.393 $C^2$, S2 : x/m = 0.436 $C^2$, S3 : x/m = 0.636 $C^2$위 식에서 보듯이 k값이 sewage sludge cake 처리수준이 증가할수록 0.393, 0.436, 0.636으로 증가하므로 TCE 처리농도가 같다면 sewage sludge cake 처리수준이 높은 토양일수록 TCE에 대한 흡착효율이 좋았다. 반면 석회시용 수준이 증가할수록 토양의 pH는 증가하였고 TCE 흡착능력은 감소하였다.

• 한국영양학회:학술대회논문집
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• 한국영양학회 2003년도 연합학술대회
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• pp.248.2-248.2
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• 2003

• 공업화학
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• 제26권4호
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• pp.432-438
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• 2015

본 연구에서는 활성탄소섬유(ACFs)에 함산소불화 표면처리를 수행하여 수용액상에 존재하는 저농도 $Cr^{6+}$ 이온의 흡착특성을 조사하였다. ACFs의 기공구조와 표면특성은 BET와 X선 광전자 분광기(XPS)를 통해 각각 확인하였다. ACFs의 함산소불화 처리는 ACFs의 표면에 중금속 흡착 능력에 영향을 미치는 C-O 결합의 비율을 크게 증가시켰으며, 그 결과 $Cr^{6+}$ 흡착이 10 min 이내에 빠르게 평형에 도달할 수 있었다. 또한 초기 $Cr^{6+}$ 농도 20 ppm에서 최대 $Cr^{6+}$ 제거효율은 미처리 ACFs와 비교하여 약 100% 증가하였다. 이러한 결과로부터 ACFs의 함산소불화 반응은 저농도 $Cr^{6+}$의 흡착을 위한 표면처리법으로 응용될 수 있을 것이다.

• Journal of Applied Biological Chemistry
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• 제51권1호
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• pp.28-35
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• 2008

The physico-chemical properties of kapok fibers were altered via the combination processes of chlorite-periodate oxidation, in order to assess their efficacy as a heavy metal adsorbent. The chemically-oxidized kapok fibers were found to harbor a certain amount of polysaccharides, together with lowered lignin content. This alteration in lignin characteristics was clearly confirmed via FTIR and NBO yield. Moreover, chemically oxidized kapok fibers retained their hollow tube shape, although some changes were noted. The chemically oxidized kapok fibers evidenced elevated ability to adsorb heavy metal ions with the best fit for the Langmuir adsorption isotherm model. Three cycles of adsorption-desorption were conducted with in-between regeneration steps. Our experimental results indicated that chemically oxidized kapok fibers possessed excellent adsorption characteristics, and the modified kapok fibers could be completely regenerated with almost equimolar diluted sodium hydroxide. Pb, Cu, Cd and Zn ions evidenced adsorption rates of 93.55%, 91.83%, 89.75%, and 92.85% on the chemically oxidized kapok fibers. The regeneration efficiency showed 73.58% of Pb, 71.55% of Cu, 66.87% of Cd, and 75.00% of Zn for 3rd cycle with 0.0125N NaOH.