• 한국구조물진단유지관리공학회 논문집
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• 제16권4호
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• pp.122-129
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• 2012

이 연구에서는 시멘트계 광물로 제조된 그라우트의 사용에 의해 발생되는 환경문제인 pH의 증가와 중금속오염을 MC계와 킬레이트고분자를 이용하여 평가하고자 하였다. 그라우트 재료로 보통포틀랜드시멘트와 슬래그시멘트를 사용하였고 급결재로 칼슘알루미네이트계 급결성재료의 혼합물을 사용하였으며, 중금속과 pH의 발생을 방지하기 위해 증점제를 사용하였다. 측정결과, 킬레이트고분자를 사용할 경우에 그라우트에 의한 pH의 증가가 최소화되었으며 중금속($Cr^{6+}$)은 용출되지 않았다. 그 이외의 경우에는 pH의 증가와 중금속 용출이 뚜렷이 증가하였다. 또한, 재령에 따른 중금속 발생량은 용출시험 1일에서 전 용출량의 약 97% 이상이 용출되었고 이후는 추가 발생되지 않는 것으로 나타났다. 이 연구의 결과로부터 pH의 증가와 $Cr^{6+}$과 같은 중금속의 용출을 제어하기 위해서 BSC와 킬레이트고분자를 사용하는 것이 아주 유용함을 알 수 있었다.

• 한국결정성장학회지
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• 제23권2호
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• pp.114-118
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• 2013

최근 금속자원 재활용과 환경보호에 대한 기술적 필요성에 의해 구리(Cu)를 주성분으로 하는 동합금으로부터 니켈, 주석 등의 유가금속 분리/회수에 대한 관심이 높아지고 있다. 본 연구에서는 동합금에 포함된 유가금속들을 분리/회수하는 기초연구중 하나로서, 킬레이트 수지를 이용하여 동합금 제련시 발생하는 부산물에 포함되어 있는 대표적인 유가금속인 니켈(Ni)을 분리/추출할 수 있는 농축 공정의 가능성에 대해 검토하였다. 킬레이트 수지는 원자량이 높은 $Cu^{2+}$ 이온을 $Ni^{2+}$ 이온보다 선택적으로 흡수하였으며, 이러한 과정을 수차례 반복함으로써 실제 동합금 부산물 샘플의 $Ni^{2+}$ 및 $Cu^{2+}$ 이온을 농축할 수 있었으며, XRF 분석을 통하여 각각 70 % 및 99 %의 농도로 분리할 수 있음을 확인하였다.

• 한국재료학회지
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• 제9권12호
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• pp.1176-1180
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• 1999

Polyetherimide와 실리콘 사이의 RIE 처리 및 알루미늄 킬레이트 계열의 adhesion promoter 처리에 따른 접착력과 고온고습환경에서의 신뢰성 변화를 연구하였다. 실험 방법으로는 180$^{\circ}$ 필 테스트 및 <85$^{\circ}C$ 85%> 테스트, SEM, AFM, 증류수 접촉각 실험이 수행되었다. $^O_2$ RIE 실험 결과 초기 접착력은 RIE 처리시간에 따라 약간의 변화를 가져왔으나 고온고습 환경에서의 저항성은 급격히 떨어지는 것이 관찰되었고 이것은 표면 거칠기의 영향이 아닌 표면의 친수성 정도에 따른 것으로 나타났다. Al-chelate adhesion promoter의 경우 초기 접착력에는 변화가 없으나 고온 고습환경에서의 저항성이 크게 증가하였는데 이것은 표면이 소수성으로 변한 데 따른 것으로 나타났다.

• Bulletin of the Korean Chemical Society
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• 제15권11호
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• pp.990-996
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• 1994

New ferrocene-based chelate amines, $Fe[C_5H_4CH(Me)NMe_2]_2\;(3), \;Fe[C_5H-3(CH(Me)NMe_2)(PPh_2)-1,2]_2\;(4),\;(C_5H_5)Fe(C_5H_3(CH_2NMe_2)(CH(CN)NMe_2-1,2)\;(6),\;and\;(C_5H_5)Fe(C_5H_3(CH_2NMe_2)(CH(Me)NMe_2-1,2)$ (7) have been prepared. The reaction and the coordination chemistry of 4 and other related compounds (S,R)-(1-N,N-dimethylaminoethyl)-2-dicyclohexylphosphino)ferrocene (CPFA) and 1,1'-bis-(diphenylphosphino)ferrocene (BPPF) with $Rh_2(OAc)_4(MeOH)_2$ were investigated. The reaction of the chiral ligand (S,R)-CPFA forms a complex of the type (${\eta}^1$-(S,R)-CPFA-P)$_2Rh_2(OAc)_4$ (8) in which the ligand is coordinated to both rhodium centers in a monodentate fashion through phosphorus. In contrast, the bisphosphine analogues such as BPPF and 4 afford chelate complexes of the type (${\eta}^2-PP)Rh_2(OAc)_4$ (9 & 10) where both ligands act as a chelate bidentate to a single rhodium atom. All these complexes were characterized by microanalytical and spectroscopic techniques. In one case, the structure of 8 was determined by X-ray crystallography. Crystals are monoclinic, space group C2 (No. 5), with a=26.389 (3), b=12.942 (1), c=11.825 (1) A, ${\beta}$=111.22(1)$^{\circ}$, V=3964.7 (8) $A^3$, Z=4, and $D_{calc}$=1.58 g $cm^{-3}$. Two Rh(II) centers are bridged by four $AcO^-$ groups in the ${\eta}^1$ : ${\eta}^1$ mode across a Rh-Rh single bond, and octahedral coordination at Rh(1) and Rh(1') is completed by axially coordinating (S,R)-CPFA and a briding $AcO^-$, respectively.

• Bulletin of the Korean Chemical Society
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• 제31권5호
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• pp.1177-1181
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• 2010

The synthesis and characterization of gold nanoparticles coated by Gd-chelate (GdL@Au) is described, where L is a conjugate of DTPA (DTPA = diethylenetriamine-N,N,N',N",N"-pentaacetic acid) and 4-aminothiophenol. These particles are obtained by the replacement of citrate from the gold nanoparticle surfaces with gadolinium chelate (GdL). The average size of GdL@Au is 12 nm with a loading of GdL reaching up to $1.4{\times}10^3$ per particles, and they demonstrate very high r1 relaxivity (${\sim}10^4mM^{-1}s^{-1}$) and the r1 relaxivity per [Gd] is as high as $10mM^{-1}s{-1}$. Here, we also describe the use of bimodality of this contrast agent (CA) as a highly efficient CT contrast agent based on gold nanoparticles (GNPs) that overcome the limitations of iodine based contrast agent. The MTT assay performed on this CAs reveals the cytotoxicity as low as that for Omniscan$^{(R)}$ in the concentration range required to obtain intensity enhancement in the in vivo MRI study.

• 펄프종이기술
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• 제47권4호
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• pp.81-87
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• 2015

Soda-AQ pulp made from sugarcane bagasse (SCB) were bleached in element chlorine free (ECF) sequence. To reduce chlorine dioxide use, final peroxide bleaching was introduced. Prior to peroxide bleaching, different chelating chemicals were applied for comparative analysis in ISO brightness and viscosity. When using equal total chlorine dioxide usage (4.5%), bleached SCB pulp using chelate and hydrogen peroxide (DEDQP) was reached 86.8% (DTPA), 86.4% (EDTA) ISO brightness, whereas bleached pulp using only hydrogen peroxide (DEDP) reached at 81.2% ISO brightness. Viscosity of DEDQP bleached pulp was 25.6 cPs (DTPA), 25.2 cPs (EDTA), And DEDP bleached pulp was shown 18.0 cPs viscosity. Decreasing of transition metal by chelate process led to improvements in final brightness along with higher viscosity. Due to EDTA is 5-7 times cheaper than DTPA, EDTA is recommended as chelating chemical prior to peroxide bleaching.

• Bulletin of the Korean Chemical Society
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• 제25권4호
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• pp.545-548
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• 2004

A sensitive, selective and rapid method for the determination of nickel based on the rapid reaction of nickel(II) with QADMAA and the solid phase extraction of the Ni(II)-QADMAA chelate with $C_{18}$ membrane disks has been developed. In the presence of pH 6.0 buffer solution and sodium dodecyl sulfonate (SDS) medium, QADMAA reacts with nickel to form a violet complex of a molar ratio of 1 : 2 (nickel to QADMAA). This chelate was enriched by solid phase extraction with $C_{18}$ membrane disks. An enrichment factor of 50 was obtained by elution of the chelates form the disks with the minimal amount of isopentyl alcohol. The molar absorptivity of the chelate was $1.32{\times}10^5L\;mol^{-1}cm^{- 1}$ at 590 nm in the measured solution. Beer's law was obeyed in the range of 0.01-0.6 ${\mu}$g/mL. This method was applied to the determination of nickel in water and biological samples with good results.

• 대한화학회지
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• 제29권4호
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• pp.372-381
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• 1985

치환 8-퀴놀린올의 옥소몰리브덴(V)착물을 합성하고 착물의 원소분석, 자외선스펙트럼, 전자스펙트럼 및 전도도를 측정하였고 옥소몰리브덴(VI)착물과 함께 질량분석을 행하여 비교 검토하였다. 옥소몰리브덴(V) 착물은 비전해질이고 몰리브덴-산소의 신축진동은 $940cm^{-1}$ 부근에서 강한 흡수띠가 나타나고 결정장전이와 전하이동 전이가 일어났다. 질량분석 결과로 Mo(V, VI)착물에서 몰리브덴과 리간드의 조성이 1:2임을 확인할 수 있었고 옥소몰리브덴(VI)착물에서는 1:1조성의 착물의 질량수가 나타나지만 옥소몰리브덴(V)에서는 일부만 확인되었다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2007년도 춘계학술대회
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• pp.804-807
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• 2007

The acid gas removal (AGR) system was designed and installed to remove $H_2S$ in coal syngas in the pilot-scale coal gasification system for producing chemicals like Dimethyl Ether(DME). The syngas from the coal gasification at the rate of $100{\sim120$ $Nm^3$/hr included pollutants such as fly ash. $H_2S$, COS, $NH_3$, etc. The designed temperature and pressure of the AGR system are below 50oC and 8 kg/$cm^2$. Fe-chelate was used as an absorbent. $H_2S$ was stably removed below 0.5 ppm in the AGR system when the concentration of $H_2S$ was $150{\sim}450$ ppm. The pH of Fe-chelate solution was also stably maintained between $8{\sim}9$. FeMgO absorbent was also tested to remove $H_2S$ in the lab-scale AGR system and $H_2S$ was also removed below 0.5 ppm in the initial operation.

• 한국응용과학기술학회지
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• 제18권4호
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• pp.254-260
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• 2001

The Mo(V) $di-{\mu}-oxo$ type [$Mo_{2}O_{4}(H_{2}O)_{2}L_{2}$] $SO_{4}$ complexes(L: 2,2'-dipyridyl,4,4'-ethylenedianlline) have been prepared by the reaction of $[Mo_{2}O_{4}(H_{2}O)_{6}]SO_{4}$ with a series of chelate ligands. These complexes are completed by two terminal oxygens arranged trans to one another and each ligand forms a chelate types. In $Mo_{2}O_{4}(H_{2}O)_{2}L_{2}$, two $H_{2}O$ coordinated at trans site of terminal oxygens. The prepared complexes have been characterized by elemental analysis, infrared spectra, $^{1}H$ nuclear magnetic resonance spectra, and thermal analysis(TG-DTA). In the potential range -0.00V to -1.00V at a scan rate of $50mVs^{-1}$, a cathodic peak at -0.81V ${\sim}$ -0.87V (vs SCE) and an anodic peak at -0.61V ${\sim}$ -0.63V (vs SCE) have been observed in aquous solution. We infer these redox are irreversible reaction.