• 한국환경과학회지
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• 제9권5호
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• pp.409-414
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• 2000

In order to examine the availability and effectiveness of crab shell for the removal of heavy metals in aqueous solution the crab shell was compared with cation exchange resin(CER), zeolite granular activated carbon (GAC) and powdered activated carbon(PAC) on aspects of heavy metal removal capacity rate and efficiency. In the removal of Pb, Cd and Cr, the heavy metal removal capacity of crab shell was higher than those of any other sorbents (CER, zeolite, GAC, PAC) and the order of heavy metal removal capacity was crab shell>CER>zeolite>PAC GAC. However in the removal of Cu, the result of crab shell was slightly lower than that of CER. The initial heavy metal removal rate was affected by the sorts of sorbents and metals. In all heavy metals the heavy metal removal rate of crab shell was higher than those of any other sorbents. Under the heavy metal concentration of 1.0 mmole/$\ell$ the heavy metal removal efficiency of crab shell was maintained as 93~100% which was much higher than those of any other sorbents.

• 한국재료학회지
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• 제14권3호
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• pp.229-234
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• 2004

All the applications of natural zeolites make use of one or more of their physical and chemical properties: adsorption, ion-exchange and related molecular sieve properties, dehydration and rehydration, and siliceous composition. Accordingly, the applications of zeolite have been carried out in the various aspects because of its large cation exchange capacity and adsorption properties. In this paper, the adsorption effect of heavy metal ions in wastewater on zeolite mineral by batch adsorption process is studied. The amounts of adsorbed ions were variable by original pH and ionic concentration, especially original pH of solution had an important effect on the adsorption. In case of low pH solution, e.g. below 3.0, clinoptilolite adsorbed $Pb^{2+}$ ,$ Cd ^{2+ }$ , $Cu^{2+}$ and $Zn^{ 2+}$ , but mordenite almost did not adsorb except $Pb^{2+}$ . Under the same conditions, these ions were more adsorbed on clinoptilolite than on mordenite mineral. The velocity of adsorption was relatively fast and it was confirmed by shaking test that the equilibrium of adsorption could be attained in about one hour. The species of exchangeable cation of zeolite had an effect on its removing ability and zeolite of the sodium-exchanged type was the best.

• 청정기술
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• 제22권3호
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• pp.161-167
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• 2016

여러 가지 금속이온이 치환된 제올라이트에서 벤젠의 촉매연소 반응에 대해 연구하였다. 사용한 제올라이트 중 Y(4.8)형 제올라이트가 가장 높은 활성을 보여주었고, Y(4.8)형 제올라이트에 치환된 금속 이온 중 구리이온이 가장 높은 활성을 보여주었다. 촉매의 활성은 산소 TPD에 의해 얻어진 흡착산소의 양에 비례하였다. Cu/Y(4.8) 촉매에서 Cu 이온의 농도가 커질수록 반응활성이 증가하였다. 벤젠의 연소반응의 전환율은 반응물 중 벤젠의 농도보다는 산소 농도의 영향을 많이 받았다. 또한, 반응물에 첨가된 물은 촉매 활성을 감소시켰다.

• Macromolecular Research
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• 제16권1호
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• pp.21-30
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• 2008

Based on the sheath-core bicomponent composite fibers with modified polystyrene (PS) and the modified polypropylene (PP), composite fibers obtained were further cross-linked and sulphonated with chlorosulphonic acid to produce strong acidic cation ion exchange fibers. The structures of the fibers obtained were characterized using Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC) etc. The optimal technology of the fibers obtained is discussed. The static absorption capacity of the sheath-core bicomponent composite cation exchange fibers for $Zn^{2+}$, $Cu^{2+}$ was determined. The absorption kinetics and major factors affecting the absorption capacities of $Zn^{2+}$, $Cu^{2+}$ were studied, and its chemical stability and regenerating properties were probed. The results suggest that cation exchange fibers with better mechanical properties and higher exchange capability were obtained. Moreover, this type of ion exchange fiber has good absorption properties and working stability to various metal ions. Hence, they have higher practicability.

• 대한화학회지
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• 제46권6호
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• pp.515-522
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• 2002

240$^{\circ}C$와 Ca/Si=2 몰 비율의 열수상태에서 합성된 고체 베타-디칼슘 실리케이트 하이드레이트($\beta-C_2$SH)는 Fe, Cu, Zn, Cd, 및 Pb와 같은 2가 금속 양이온에 대한 양이온 교환 성질을 보여준다. 그 고체에 희한 금속 양이온 흡인력은 $Fe^{2+}$〉$Cu^{2+}$〉$Zn^{2+}$〉$Cd^{2+}$ = $Pb^{2+}$의 순서로 됨이 밝혀졌다. 고체에 세슘 선택성은 $Li^+$, $Na^+$ 및 $K^+$와 같은 1가 양이온이나 $Ca^{++}$, $Mg^{++}$ 및 $Ba^{++}$와 같은 2가 양이온이 $Cs^+$보다 백배이상 진한 상태에서 나타내었다. $Cs^+$의 흡인력은 $Mg^{++}$의 존재하에서 최대치를 보여주었고, 반면에 $K^+$의 존재하에서 최소치를 보여주었다. 2가 금속이온에 대한 $\beta-C_2$SH의 다른 친화도는 이들 이온을 분리하는데 사용 할수 있다. 또한 $\beta-C_2$SH에 희한 금속 양이온 교환에 대한 반응경로 및 세슘 선택성이 연구되었다.

• 한국표면공학회지
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• 제52권6호
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• pp.334-341
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• 2019

Organometal halide perovskite materials have attracted much attention in the photovoltaic and light emitting devices due to the compositional flexibility with AMX₃ formula (A is an organic amine cation; M is a metal ion; X is a halogen atom). The addition of homovalent or heterovalent metal cations to the bulk organohalide perovskites has been performed to modify their energy band structure and the relevant optoelectronic properties by ligand-assisted ball milling. Here, we report CH₃NH₃Pb_1-xM_xBr₃ nanocrystals substituted by metallic cations (M is Sn²⁺, In³⁺, Bi³⁺; x = 0, 0.01, 0.02, 0.05, 0.1, 0.2). Photoluminescence and quantum yield was significantly reduced with increasing metallic cations content. These quenching effect could be resulted from the metal cations that behave as a non-radiative recombination center.

• 공업화학
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• 제16권6호
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• pp.857-864
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• 2005

탈알루미늄 및 알칼리/알칼리토금속 양이온으로 치환한 Y형 및 ZSM-5 제올라이트 촉매를 제조하였다. 전처리 후 Y형 및 ZSM-5 제올라이트의 Si/Al비는 증가하였고, bulk보다는 표면에서의 Si/Al비가 더 큰 것을 알 수 있었다. 전처리에 의해 제조된 Y형 및 ZSM-5 제올라이트의 골격구조 파괴는 주로 탈알루미늄 처리과정에서 Al 이온의 탈리에 의한 것이며, framework이 감소하고 non-framework이 증가하였다. 이러한 현상은 스팀처리 시간이 많아질수록 증가하였고, 양이온으로 치환함에 따라 더욱 심화되었음을 알 수 있었다. NO-TPD 실험결과, 전처리된 Y형 및 ZSM-5 제올라이트는 탈착봉우리가 저온으로 이동하였다. 또한 스팀처리 시간이 많은 촉매물질일수록 탈착온도가 더 낮은 온도로 이동하였다. 촉매의 활성은 치환된 양이온, Si/Al 함량비 및 탈알루미늄으로 변화된 골격구조에서 framework과 non-framework의 비율에 의존하였다.

• Journal of Electrochemical Science and Technology
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• 제2권3호
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• pp.143-145
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• 2011

Metal-binding antibiotics are very attractive choices as cation selective ionophores. The ability of tetracycline (TC) antibiotics to bind to metal ions has obtained much attention. TCs exhibit the potentiometric performance changes for various cations dependant on several experiment conditions. In this report, we investigated the potentiometric performance changes of TC as the modification of TC's possible metal binding site. We found that the selectivity alter with the blocking main binding site of ionophores for cations. And, additionally it is possible to control the selectivity of sensors with chemical modification of ionophores.

• Bulletin of the Korean Chemical Society
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• 제4권2호
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• pp.76-79
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• 1983

The elution behaviors of a series of metal complexes, such as $Co(gly)_{3}$, $[Ni(en)_{3}]^{2+}$, $[Ni(phen)_3]^{2+}$, $[Fe(phen)_3]^{2+}$, $[Co(phen)_3]^3+$, $[Co(tn)_3]^3+$, $[Co(en)_3]^3+$ and $[Co(NH_3)_6]^3+$ (where gly; glycine, phen; phenanthroline, tn; trimethylenediamine, en; ethylenediamine), were studied in aqueous solution by measuring the retention volumes (v values) on SP-Sephadex C-25, cation exchange resin. It was found that the elution behaviors of metal complexes were apparently affected by salt concentrations, kinds of cations in eluent and kinds of anions in eluent, and according to the degrees of their effects coulombic forces, ion exchange capacities, the 'solvent effect' of resin backbone, hydrophobicity and hydrophilicity were applied to explain the elution mechanism.

• Bulletin of the Korean Chemical Society
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• 제19권2호
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• pp.207-211
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• 1998

Potentiometric characteristics of DOS plasticized PVC-based membranes containing upper-rim calix[4]crown neutral carrier to various metal cations and protonated alkylamines have been examined. Although the calix[4]crown-based membrane electrodes exhibited substantial emf responses to alkali and alkaline earth metal cations, their high detection limits (- log[Cs+]=4.5) and sub-Nernstian response slopes (48 mV/pCs+) to the most selective cation, cesium, indicate that the metal cation complexing ability of calix[4]crown is much weaker than that of macrocyclic crown ethers. However, the calix[4]crown-based membrane electrodes exhibited near-Nernstian response slopes (56 mV/decade for hexylNH3+) with low detection limits (log[hexylNH3+]= - 6.7) to most alkylammonium ions compared to those of blank (DOS plasticized PVC membrane with no ionophore) or crown ether-based membranes. While the selectivity patterns of blank and crown ether-based membranes are determined primarily by the lipophilicity of alkylammonium ions, the membranes doped with calix[4]crown ionophore could effectively discriminate the steric shapes of nonpolar alkyl groups of alkylammonium ions.