• 한국수소및신에너지학회논문집
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• 제22권6호
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• pp.780-786
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• 2011

Mg hydride had high hydrogen capacity (7.6%), lightweight and low cost materials and it was promising hydrogen storage material at high temperature. However, commercial applications of the Mg hydride are currently hindered by its high absorption/desorption temperature, and very slow reaction kinetics. one of the approaches to improve the kinetic is $MgH_x$ intermixed with carbon. And it shows that carbon and carbon allotropes have a beneficial effect on hydrogen sorption in Mg. The graphene is a kind of carbon allotropes which is easily desorbed reaction at low temperatures because its reaction is exothermic. In this work, the effect of graphene concentration on the kinetics of Mg hydrogen absorption reaction was investigated. The $MgH_x$-Graphene composites has been prepared by hydrogen induced mechanical alloy (HIMA). The synthesized powder was characterized by XRD and simultaneous TG, DSC analysis. The hydrogenation behaviors were evaluated by using a sievert's type automatic PCT apparatus. In this research, results of kinetic profiles exhibit hydrogen absorption rate of $MgH_x$-5wt.% and 10wt.% graphene composite, as 1.25wt.%/ms, 10.33wt.%/ms against 0.88wt.%/ms for $MgH_x$ alone at 473K.

• 대한토목학회논문집
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• 제29권1B호
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• pp.91-96
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• 2009

LDH(Layered double hydroxide) 물질을 제조하고 이를 이용하여 비소를 흡착시키는 실험을 수행하였다. TEM을 이용하여 제조한 LDH 물질의 형상을 살펴본 결과 열처리를 거친 시료는 나노크기의 결정화된 구조를 가지고 있고 열처리를 거치지 않은 시료는 아직 결정화가 완전히 이루어지지 않았으며 크기도 마이크로 범위에서 나타났다. X선 회절분석 결과를 보면 이 같은 결과가 뚜렷이 나타났으며, 열처리를 거친 경우는 뚜렷한 결정화를 보이고 있었다. $N_2$ 흡착 및 탈착 결과를 통해 LDH가 mesoporous한 공극 형태를 가지고 있다는 것을 알 수 있었다. 비표면적은 열처리를 거친 시료가 열처리를 거치지 않은 시료보다 2배 이상 크게 나타났다. 흡착 등온 실험 결과에서도 두 시료는 비슷한 흡착량을 보이며 기존 철산화 물에 못지않은 흡착능을 나타내고 있다. 금번에 합성한 Mg Fe-LDH 물질을 이용하여 토양 및 지하수의 비소 제거 공정에 적용할 수 있음을 확인하였다.

• 자원리싸이클링
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• 제25권4호
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• pp.60-67
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• 2016

본 연구에서는 P507을 포함하고 있는 추출수지를 사용하여 중희토류 원소인 Gd, Tb, Dy의 흡 탈착 반응 메커니즘을 고찰하고 분리를 위한 최적 크로마토그래피법의 반응조건을 도출하였다. 흡 탈착 반응 메커니즘은 흡착등온식인 Langmuir, Freundlich 흡착등온식과, 흡착속도모델인 유사 1차, 2차 반응속도식을 적용하여 고찰하였다. 중희토류 원소의 흡착반응은 단분자층으로 일어난다고 가정하여 흡착등온식을 적용하였고, 잘 일치하여 흡착반응이 단분자층으로 이루어짐을 추측할 수 있었다. 시간별 실험을 진행하여 유사 1차, 2차 반응속도식에 적용한 결과 유사 2차 반응속도식이 추출수지의 중희토류 흡착 메커니즘을 더 잘 표현하였고, 평형흡착량의 실험값은 이론값에 부합하였다. 크로마토그래피법을 이용하여 용리액 HCl 0.25 M 농도조건에서 ${\alpha}^{Tb}_{Gd}=1.24$, ${\alpha}^{Dy}_{Tb}=1.03$으로 분리계수 1이상의 높은 분리조건을 확인하였다. HCl 용리액을 사용하였을 때, 용리액의 농도가 높을수록 분리도는 감소하고 용출구간은 줄어드는 경향을 확인하였다.

• Food Science and Biotechnology
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• 제16권5호
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• pp.771-777
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• 2007

Sliced and whole root of rehmannia were dehydrated in a laboratory dryer at 40, 60, 80, and $100^{\circ}C$ to evaluate the kinetic parameters for dehydration of rehmannia. The drying curves of both samples were characterized by a falling-rate drying period only. Sliced rehmannia dried 1.1 to 3.1 times faster than whole root of rehmannia depending on drying temperature. Equilibrium moisture content (EMC) of rehmannia samples at the drying temperature tested were 0.069-0.078 g water/g dry solid, which was coincided with the monolayer moisture content (0.06 and 0.07 g water/g dry solid) evaluated from desorption isotherms using GAB (Guggenheim-Anderson-de Boer) model. A logarithmic model for thin layer drying was applied to evaluate the drying time to reach EMC ($t_{EMC}$) and drying constant (k). The effect of temperature on $1/t_{EMC}$ and k was described by the Arrhenius model with activation energy values of 32.56 and 47.14 kJ/mol determined using the former parameter, and 34.27 and 38.26 kJ/mol determined using the latter parameter for sliced and whole root of rehmannia, respectively.

• 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.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2011년도 제40회 동계학술대회 초록집
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• pp.338-338
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• 2011

The behavior of hydroxide ions on water-ice films was studied by using $Cs^+$ reactive ion scattering (RIS), low energy sputtering (LES) and temperature-programmed desorption (TPD). A $Cs^+$ beam of a low kinetic energy (<100 eV) from $Cs^+$ ion gun was scattered at the film surface, and then $Cs^+$ projectiles pick up the neutral molecules on the surface as $Cs^+$-molecule clusters form (RIS process). In LES process, the preexisting ions on the surface are desorbed by the $Cs^+$ beam impact. The water-ice films made of a thick (>50 BL) $H_2$O layer and a thin $D_2O$ overlayer were controlled in temperatures 90~140K. We prepared hydroxide ions by using Na atoms which proceeded hydrolysis reaction either on the ice film surface or at the interface of the $H_2O$ and $D_2O$ layers.[1] The migration of hydroxide ions from the $H_2O/D_2O$ interface to the top of the film was examined as afunction of time. From this experiment, we show that hydroxide ions tend to reside at the water-ice surface. We also investigated the H/D exchange reactions of $H_2O$ and $D_2O$ molecules mediated by hydroxide ions to reveal the mechanism of migration of hydroxide to the ice surface.

• 한국수소및신에너지학회논문집
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• 제23권5호
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• pp.429-436
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• 2012

Mg and Mg-based alloys are regarded as strong candidate hydrogen storage materials since their hydrogen capacity exceeds that of known metal hydrides. One of the approaches to improve kinetic is addition of metal oxide. In this paper, we tried to improve the hydrogenation properties of Mg-based hydrogen storage composites. The effect of transition metal oxides, such as $Nb_2O_5$ on the kinetics of the Magnesium hydrogen absorption kinetics was investigated. $MgH_x$-5wt.% $Nb_2O_5$ composites have been synthesized by hydrogen induced mechanical alloying. The powder fabricated was characterized by X-ray diffraction (XRD), Field Emission-Scanning Electron Microscopy (Fe-SEM), Energy Dispersive X-ray (EDX), BET and simultaneous Thermo Gravimetric Analysis / Differential Scanning Calorimetry (TG/DSC) analysis. The Absorption / desorption kinetics of $MgH_x$-5wt.% $Nb_2O_5$ (type I and II) are determined at 423, 473, 523, 573 and 623 K.

• Korean Journal of Chemical Engineering
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• 제35권11호
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• pp.2198-2206
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• 2018

We addressed the development of a novel, low-cost, and high-efficient material from hybrid materials, known as microcapsules. Microcapsules are a composite adsorbent made of a mixture of tannin, sericite and chitosan. The FT-IR analysis showed that the microcapsules contain hydroxyl, carboxyl, carbonyl, and amino groups, which play an important role in the adsorption of heavy metals. The microcapsules were able to remove 99% of Pb(II) in 30 min, and obtained a removal efficiency of more than (13-50)%, compared with the single adsorbents of tannin, chitosan, and sericite. In adsorption kinetic analysis, pseudo-second-order adsorption was more suitable than pseudo-first-order adsorption, and chemical adsorption did not limit the adsorption rate of Pb(II) ion. In isothermal adsorption, Langmuir adsorption was more suitable than Freundlich adsorption, and the maximum Langmuir adsorption capacity was 167.82 (mg/g). Furthermore, desorption and reusability studies, as well as the applicability of the material for wastewater treatment, demonstrated that microcapsules offer a promising hybrid material for the efficient removal of significant water pollutants, i.e., Pb(II) from aqueous solutions.

• 대한환경공학회지
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• 제31권8호
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• pp.663-672
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• 2009

본 연구는 조류 Chlorella pyrenoidosa에 의한 Pb 흡착시 고정화 방법이 흡착특성에 미치는 영향에 관한 것으로, 고정화는 Ca-alginate, K-carrageenan, and polyacrylamide를 이용하여 실시하였다. 연구결과, 고정화에 따라 흡착평형 도달시간의 지연이 나타났으며, Pb의 최대 흡착능(mg/g)은 중금속 농도와 pH가 높을수록, 고정체 투입량이 적을수록 높게 나타났다. 고정화 방법별 흡착능은 Ca-alginate로 고정화한 경우 가장 높은 흡착능을 나타낸 반면, 흡착량이 pH에 가장 민감하게 영향을 받았다. Pb 흡착현상은 Freundlich 등온흡착식에 의해 잘 해석되었고, 흡착속도는 2차 모형식을 따르는 것으로 나타났다. FT-IR분석으로 Chlorella pyrenoidosa에 의한 Pb의 생물흡착 메커니즘이 주로 carbo-acid와 amide 그룹에 Pb가 결합되어 일어남을 알 수 있었다. 흡착된 Pb의 탈착은 탈착제 농도가 높을수록 탈착 효율도 높았다. 실험에 사용되어진 여러 탈착제(NTA, HCl, EDTA, $H_2SO_4,\;Na_2CO_3$)중 Ca-alginate과 K-carrageenan로 고정화한 경우 NTA가 가장 높게 나타났으며, polyacrylamide로 고정한 경우 EDTA를 사용한 경우 가장 효과적인 것으로 나타났다. 고정화 방법별 최대 탈착효율은 각각 90.0, 83.0, 80.0% 이었다.

• 청정기술
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• 제21권3호
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• pp.164-170
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• 2015

본 연구에서는 polysulfone과 Escherichia coli biomass의 현탁액을 방사하여 입상화한 PS-E. coli biomass composite fiber (PSBF)와 PSBF에 존재하는 아민기를 메틸화시킨 amine-methylated PSBF (AM-PSBF)를 제조하였다. PSBF와 AM-PSBF에 의한 염기성 염료 Basic Blue 3 (BB3)의 흡착특성을 비교함으로써 아민기의 메틸화가 BB3의 흡착에 미치는 영향을 확인하였다. pH edge 실험에서는 두 흡착제 모두 pH가 증가할수록 BB3 흡착량이 증가하는 경향을 보였고, 동일 pH에서 AM-PSBF가 PSBF보다 높은 흡착량을 나타내었다. PSBF와 AM-PSBF 모두 흡착평형은 5시간 이내에 도달하였으며, 흡착속도론 실험 데이터는 유사 1차 속도 모델식으로 잘 묘사되었다. 그리고 Langmuir 모델에 따르면, pH 8에서 AM-PSBF의 최대흡착량은 28.9 mg/g로 PSBF의 최대흡착량인 20.7 mg/g보다 약 1.4배 증가하였다. 이 결과로부터 PSBF에서 아민기의 메틸화는 염기성 염료의 흡착을 향상시키는 효과가 있음을 알 수 있다. 또한, 탈착실험 결과는 AM-PSBF가 반복적으로 재사용 될 수 있음을 보여주었다.