• Environmental Engineering Research
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• 제22권1호
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• pp.95-107
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• 2017

Adsorption equilibrium and kinetic behavior of two toxic heavy metals hexavalent chromium [Cr(VI)] and mercury [Hg(II)] on mustard oil cake (MOC) was studied. Isotherm of total chromium was of concave type (S1 type) suggesting cooperative adsorption. Total chromium adsorption followed BET isotherm model. Isotherm of Hg(II) was of L3 type with monolayer followed by multilayer formation due to blockage of pores of MOC at lower concentration of Hg(II). Combined BET-Langmuir and BET-Freundlich models were appropriate to predict Hg(II) adsorption data on MOC. Boyd's model confirmed that external mass transfer was rate limiting step for both total chromium and Hg(II) adsorptions with average diffusivity of $1.09{\times}10^{-16}$ and $0.97m^2/sec$, respectively. Desorption was more than 60% with Hg(II), but poor with chromium. The optimum pH for adsorptions of total chromium and Hg(II) were 2-3 and 5, respectively. At strong acidic pH, Cr(VI) was adsorbed by ion exchange mechanism and after adsorption reduced to Cr(III) and remained on MOC surface. Hg(II) removal was achieved by complexation of $HgCl_2$ with deprotonated amine ($-NH_2$) and carboxyl (COO-) groups of MOC.

• Carbon letters
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• 제3권4호
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• pp.219-225
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• 2002

The two-step surface modifications of activated carbon was carried out to improve the adsorption capacity of toxic heavy metal ions in liquid phase. Physical and chemical properties of the as-received activated carbon (AC) and two kinds of surface-modified activated carbons ($1^{st}AC$ and $2^{nd}AC$) were evaluated through the BET analysis, surface acidity, and oxides measurements. Specific surface area and pore volume did not significantly change, but surface oxide-group remarkably increased by the surface modification. Equilibrium and batch adsorptions of the various metals, such as Pb, Cd, and Cr, using AC, $1^{st}AC$, and $2^{nd}AC$ were performed at initial pH 5. The adsorption capacity and rate of $2^{nd}AC$ were higher than those of AC and $1^{st}AC$. The carboxylic/sodium carboxylate complex groups were developed from the two-step surface modification of activated carbon, which strongly affected the adsorption of metal ions.

• 대한전자공학회논문지
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• 제27권12호
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• pp.1859-1864
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• 1990

The effect of H+ and OH- ion concentrations at doped Si semiconductor/pH buffer solution interfaces were investigated in terms of cyclic current-voltage characteristics. The effects of space charge on oppositely doped Si semiconductors, i.e., p-and n-Si semiconductors, can be effectively applied to study the pH effects and the slow surface states at the interfaces. The adsorptions of H+ and OH- inons on the doped Si semiconductor surfaces are physical adsorption rather than chemical adsorption. Adsorptive processes and charging effects of the slow surface states can be explained as the potential barrier variations and the related current-voltage characteristics at the interfaces. Under forward bias, the charged slow surface states on the p-and n-si semiconductor surface are donor and acceptor slow surface states, respectively. The effects of minority carriers on the slow surface states can be neglected at the doped Si semiconductor interfaces.

• 한국재료학회:학술대회논문집
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• 한국재료학회 1998년도 IUMRS-ICEM ABSTRACT BOOK
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• pp.141.4-141
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• 1998

• Bulletin of the Korean Chemical Society
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• 제30권8호
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• pp.1805-1810
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• 2009

The adsorptions of trimethygallium (TMG) and arsine (As$H_3$) on H/Si(100)-2x1 surface were theoretically investigated. In the case of TMG adsorption, methane loss reaction, surface methylation, hydrogen loss reaction and ring closing reaction channels were found. The mechanism of As$H_3$ adsorption on the surface was also identified. Among these, the methane loss reaction depositing –Ga(C$H_3)_2$ was found to be the major channel due to its low barrier height and the large exothermicity. The surface methylation reaction is the second most favorable channel. In contrast, arsine turned out to be less reactive on the surface, implying that Arsine surface reaction would be the rate limiting step in the overall ALD process.

• 대한전자공학회논문지
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• 제27권7호
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• pp.1042-1048
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• 1990

The approximations of charge relationships at normally doped semiconductor interfaces were qualitatively derived basis on electrical neutrality conditions. Effects of ion adsorptions, activation processes, interfacial structures, rectifying phenomena, and effects of surface potential barriers at the p- and n-Si/CsNO3 aqueous electrolytes, and the p-Si/(1HF:3HNO3:6H2O) electrolyte solutions were investigated using a cyclic voltammetric method. The space charge acts the most important role for the pn junction structures, the rectifying phenomena, and the activation processes. The Current-Voltage (I-V) characteristics curves significantly depend on developing of the Helmholtz double layers and charging of the show surface states during the activation processes. A linear Current-Voltage characteristics region was observed at the p-Si/(1HF:3HNO3: 6H2O) electrolyte solution interface.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2012년도 춘계학술발표회 논문집
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• pp.216-217
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• 2012

QM/MM 혼성 이론 방법인 ONIOM 계산을 통해, $CO_2$가 $B_N$-BNNT 벽면에서의 흡착 반응과 $H_2CO_3$로의 전환 반응 메커니즘을 규명함으로써 $B_N$-BNNT가 효과적인 $CO_2$ 흡착제와 $H_2CO_3$ 생성 반응 촉매로 개발 가능함을 확인하였다.

• KSBB Journal
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• 제15권5호
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• pp.444-451
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• 2000

Nonliving methanotrophic biomass was used as biosorbent to remove lead which is one of representative pollutants in metal-bearing wastewater. Solution pH, maximum uptake, biosorbent dose and ionic strength were considered as major factors for adsorption experiments. The optimum pH range for lead removal was increased 3.8∼11.0 for methanotrophic biomass compared to biosorbent-free control, pH of 8.4∼11.2. Removal efficiency of lead by methanotrophic biomass was pH dependent, but less sensitive than that of control. In isotherm experiments with 0.2g biosorbent/L at initial solution pH 5.0, methanotrophic biomass took up lead from aqueous solutions to the extent of 1085 mg/g biomass. Removal amount of lead increased with an increase of biomass dose. According to biomass dose for initial 1000 mg Pb/L at initial pH 5.0, the optimum amount of biomass for maximum lead removal per unit methanotrophic biomass was 0.2 g biomass/L. As a result of scanning electron microscope (SEM) micrographs equipped with energy dispersive spectroscopy (EDS), lead removal by methanotrophic biomass seemed to be through adsorptions on the surface of methanotrophic biomass and exopolymers around the biomass. EDS spectra confirmed that lead adsorption appeared on the biomass and exopolymers that may be effective to lead removal comparing before and after contact with lead. Removal efficiency of lead was slightly affected by ionic strength up to 2.0 M of NaCl and NaNO$_3$respectively.

• 한국식품영양학회지
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• 제9권3호
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• pp.299-306
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• 1996

The study was performed under the various conditions, such as the edible parts and particle sizes of Allium. The concentrations, the temperartures, and the pH of heavy metal solutions to investigated their adsorption capacity of heavy metals by genus Allium. The adsorption amount of Pb by Allium in the aqueous soluton was apparently higher than that of Ni and Cu by them. The larger the particle sloe of welsh onion and shallot was, the higher the adsorption of Cu was. The adsorptlons of Cu, Ni and sorption ratio was not different. As the temperature increased, the amount of heavy metal adsorption increased in general, but the adsorption of Ni by welsh onion and wild garlic and leek, Cu by shallot, wild garlic and leek decreased. Adsorption of Pb to Allium was not affected by the different values of pH, and adsorptions of Ni and Cu were greatly affected by those of pH. Especially, the higher the pH was, the greater the Ni adsorption to Allium was, and the lower the pH was, the higher the Cu adsorption was. The correlation between the amount of components in edible parts of Allium and that of adsorption of heavy metals was significantly high In amino acids containing sulfhydryl group(-SH) and vitamin B2.

• 상하수도학회지
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• 제26권2호
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• pp.275-283
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• 2012

MCM-41(Mobil's Composition of Matter-41) and expanded graphite(EG) were investigated as potential adsorbents for heavy metal ions including Pb(II), Cu(II) and Ni(II) in various aqueous chemistries. MCM-41 showed shorter equilibrium times and higher adsorption capacities for all three heavy metal ions compared to expanded graphite. The adsorption of three heavy metal ions was significantly affected by the solution pH due to the competition with $H_{3}O^{+}$ at lower pH and precipitation at neutral or higher pH. Adsorptions of heavy metal ions onto MCM-41 and expanded graphite were successfully described with the pseudo-second-order model. During the competitive adsorption of three heavy metal ions, the selectivity of Pb(II) was highest and almost same selectivity was observed with Cu(II) and Ni(II) when MCM-41 was used as an adsorbent, while the expanded graphite exhibited the highest selectivity to Pb(II), followed by Ni(II) and Cu(II).