Conducting Cell Scaffold—Poly(3′-aminomethyl-2,2′:5′,2′′-terthiophene)

정의덕,황재영,이주운 대한화학회 2015 Bulletin of the Korean Chemical Society Vol.36 No.4

Electroactive biomaterials such as polythiophene (PT) are highly attractive scaffolds for tissue engineering applications. The introduction of reactive functionalities into the PT backbone structure is desired to enhance the biomaterial-tissue interface for desired tissue responses. Here, we present amino-functionalized conductive polyterthiophene, poly(3′-aminomethyl-2,2′:5′,2′′-terthiophene) (PTTh-NH2), which successfully demonstrates the potential to influence cellular activity. The chemical structure of monomeric 3′-aminomethyl-2,2′:5′,2′ ′ -terthiophene was confirmed by MS and the polymer characteristics of PTTh-NH2 were determined by AFM, XPS, profilometer and four-point probe. In vitro cell viability study with human umbilical vascular endothelial cells (HUVECs) indicates that the primary amine functionality grafted into polythiophene (PT) backbone improve the cell adhesion and proliferation compared to negative (−) control conventional PT. Thus, PTTh-NH2 could be useful in developing PT composites for various biomedical applications.

Metal-ion dependent band energetics in SrM0.5Ti0.5O3 (M =Ru, Rh, Ir, Pt, Pd) like structures for solar applications

정의덕,J. S. Jin,H. J. Kim,홍태은,조채용,K. T. Lim,김현규,P. H. Borse 한양대학교 세라믹연구소 2011 Journal of Ceramic Processing Research Vol.12 No.6

We present here a detailed comparative study of the theoretically-calculated electronic structures of the cubic Sr M0.5Ti0.5O3(M: Ru, Rh, Ir, Pt, Pd) type and SrTiO3 system. A their full potential linearized augmented plane wave (FP-LAPW) method was used to obtain its band structure within the framework of a density functional theory by using Wien97 code. The 4d orbitals of Ru, Rh and 5d orbitals of Ir, Pt respectively, contribute to the top of the valence band yielding a band gap narrowing of cubic SrTiO3. The computed tolerance factor for the SrTi0.5Pd0.5O3 perovskite structure indicates an unstable structural formation with Pd metal ion. The computation of the frequency-dependent absorption coefficient I(ω) of SrTi0.5M0.5O3indicates that Rh has a significant absorption efficiency for low energy (E ≤ 2ev) photons, whereas Ru and Ir display a very high absorption efficiency for photons with E > 2eV. Theoretical prediction validates that Rh can yield a better solar photoactive material than Ru and Ir in the SrTi0.5M0.5O3 (M:Ru, Rh, Ir) type system for low energy photon applications.

졸-겔 방법에 의한 LiMn₂O₄의 합성 및 전기화학적 거동

정의덕,문성욱,이학명,원미숙,윤장희,박덕수,심윤보,Jeong, Euh-Duck,Moon, Sung-Wook,Lee, Hak-Myoung,Won, Mi-Sook,Yoon, Jang-Hee,Park, Deog-Su,Shim, Yoon-Bo 한국전기화학회 2003 한국전기화학회지 Vol.6 No.4

리튬이온전지 양극재료로서 리튬막간계 산화물을 졸겔 방법으로 전구물질을 합성하여 $400^{\circ}C$와 $800^{\circ}C$에서 열처리하여 합성하였다. 출발물질로는 $(CH_3)_2CHOLi$와 $Mn(CH_3COO)_2\;{\cdot}4H_2O$를 사용하였다 열분석 측정을 통해 열처리 조건을 정하였다. 또한 합성된 물질은 X-선 회절분석으로 구조를 확인하였으며 형상 및 입자의 크기는 주사전자현미경으로 측정하였다. 전기화학적 특성은 1.0M $LiClO_4/propylene\;carbonate(PC)$ 전해액 조건에서 순환전압전류법, chronoamperometry, 교류 임피던스 법 및 정전류 충$\cdot$방전 특성을 조사하였다. 교류 임피던스 법으로 확산계수를 측정한 결과 $6.2\times10^{-10}cm^2s^{-1}$를 나타내었다. A precursor of lithium manganese oxide was synthesized by mixing $(CH_3)_2CHOLi\;with\;Mn(CH_3COO)_2{\cdot}4H_2O$ in ethanol using a sol-gel method, then heat-treated at $400^{\circ}C\;and\;800^{\circ}C$ in air atmosphere. The condition of heat treatment was determined by thermogravimetric analysis/differential thermogravimetric analysis (TGA/DTA). The characterization of the lithium manganese oxide was done by X-ray diffraction (XRD) spectra and scanning electron microscopy (SEM). The electrochemical characteristics of lithium manganese oxide electrode for lithium ion battery were measured by cyclic voltammetry (CV), chronoamperometry and AC impedance method using constant charge/discharge process. The electrochemical behaviors of the electrode have been investigated in a 1.0M $LiClO_4/propylene$ carbonate electrolyte solution. The diffusivity of lithium ions, $D^+\;_{Li}\;^+$, as determined by AC impedance technique was $6.2\times10^{-10}cm^2s^{-1}$.

${\iota}$ -Sparteine으로 변성된 Carbon Paste 전극을 사용한 Co(II) 이온의 펄스 차이 전압-전류법 정량

정의덕,원미숙,박덕수,심윤보,최성낙,Eu-Duck Jeong,Mi-Sook Won,Deog-Su Park,Yoon-Bo Shim,Sung-Nak Choi 대한화학회 1993 대한화학회지 Vol.37 No.10

코발트(II) 이온의 정량을 위해 ${\iota}$-sparteine(SP)으로 변성된 탄소 반죽 전극(carbon paste electrode : CPE)을 제작하였다. 수용액 중의 코발트 이온을 CPE에 처리시킨${\iota}$-sparteine과 반응시켜서 착화합물 상태로 전극표면에 석출시킨 후, 이 착물을 전압-전류법을 사용하여 정량하였다. 또한 변성된 CPE의 전극반응을 순환 전압-전류법을 사용하여 아세트산/아세트산염 완충용액에서 조사하였다. 한번 사용한 전극은 산용액으로 처리하여 5회 이상 재사용할 수 있었다. CPE에 흡착된 Co(II)-SP 착물의 산화환원 전위는 0.17V / 0.27V였으며 산화피이크는 0.17V의 환원피이크를 지나야 나타나는 피크이다. 이는 전극표면의 SP와 용액내의 Co(II)이온이 착물을 형성하여 흡착되고, 이 전극표면에 형성된 착물이 산화환원되어 나타나는 피이크이다. 펄스차이 전압-전류법을 사용할 경우 $2{\times}10^{-7}$M 농도까지 직선적으로 감응함을 알 수 있었으며, 그 때의 상대표준 편차는 ${\pm}$5.6%이었다. 이 경우 검출한계는 $1.0{\times}10^{-7}$M이었다. 리간드와 착물을 형성할 것으로 예상되는 여러 금속이온에 대한 방해작용을 조사하였다. A cobalt(II) ion-selective carbon-paste electrode (CPE) was constructed with ${\iota}$-sparteine. Cobalt(II) ion in aqueous solution was chemically deposited through the complexation with ${\iota}$-sparteine onto the CPE. The surface of CPEs were characterized by cyclic voltammetry and differential pulse voltammetry in an acetate buffer solution, separately. Exposure of the CPEs to an acid solution could regenerate surface to reuse it for the deposition. In more than 5 deposition / measurement / regeneration cycles, the response was reproducible and linear up to $5.0{\times}10^{-6}$M with linear sweep voltammetry. The peaks at 0.17V / 0.27V were correspond to the redox of Co(II)-SP complex deposited on CPE. The anodic peak of which appeared after scan over the cathodic peak of 0.17 V to more negative scan. In case of using the differencial pulse voltammetry (DPV), we have obtained the linear response $2.0{\times}10^{-7}$M with relative standard deviation ${\pm}5.6%$. The detection limit was $1.0{times}10^{-7}$M for 20 minutes of the deposition. We have also investigated the interference effect of various metal ions, which are expected to form the complex with the ligand on the electrode.

유기산 추출에 의한 철 폐광산 오염토양의 복원

정의덕,강신원,백우현 한국환경과학회 2000 한국환경과학회지 Vol.9 No.1

A study on the remediation of heavily Fe ion contaminated soils from abandoned iron mine was carried out, using ex-situ extraction process. Also, oxalic acid as a complex agent was evaluated as a function of concentration, reaction time and mixing ratio of washing agent in order to evaluate Fe removability of the soil contaminated from the abandoned iron mine. Oxalic acid showed a better extraction performance than 0.1N-HCI, i.e., the concentrations of Fe ion extracted from the abandoned mine for the former at uncontrolled pH and the latter were 1,750 ppm and 1,079 ppm, respectively. The optimum washing condition of oxalic acid was in the ratio of 1:5 and 1:10 between soil and acid solution during 1 hr reaction. The total concentrations of Fe ion by oxalic acid and EDTA at three repeated extraction, were 4,554 ppm and 864 ppm, respectively. The recovery of Fe ions from washing solution was achieved, forming hydroxide precipitation and metal sulfide under excess of calcium hydroxide and sodium sulfide. In addition, the amounted of sodium sulfide and calcium hydroxide for the optimal recovery of Fe were 15g/ℓ and 5g/ℓ from the oxalic acid complexes, respectively.

L-Sparteine 수식전극을 사용한 Hg (II) 이온의 정량

정의덕,원미숙,심윤보,Euh Duck Jeong,Mi-Sook Won,Yoon-Bo Shim 대한화학회 1991 대한화학회지 Vol.35 No.5

A mercury ion-sensitive carbon-paste electrode (CPE) was constructed with l-sparteine. Mercury (II) ion was chemically deposited by the complexation with l-sparteine onto the CPE. The surface of CPEs was characterized by cyclic voltammetry and anodic stripping voltammetry in an acetate buffer solution, separately. Exposure of CPEs to acid solution could regenerate surface and reuse it for deposition. In 5 deposition/measurement/regeneration cycle, the response was reproducible and in licnear up to $2.0\;{\times}\;10^{-6}$ M with linear sweep voltammetry. In case of using the differential pulse technique, we have obtained the linear response up to $7.0 {\times}10^{-7}$ M with relative standard deviation of ${\pm}5.1$%. The detection limit was $5.0{\times}10^{-7}$ M for 20 minutes of the deposition. We have investigated the interference effect of various metal ions, which are expected to form the complex with ligand. Silver (I) ion of these has interfered with the analysis of Hg (II) ions. However, pretreatment of the silver (I) ion with potassium chloride led to no interference on the analysis of mercury ions in aqueous solution. 수은 이온의 정량을 위해 l-sparteine으로 처리한 carbon paste 전극(CPE)을 제작하였다. 수용액중의 수은 이온을 CPE에 수식 시킨 l-sparteine과 반응시켜 착화합물 상태로 전극표면에 석출시킨 후 이 착물을 벗김 전압-전류곡선법을 사용하여 정량하였다. 또한 수식된 CPE의 전극반응을 순환 전압 전류 곡선법을 사용하여 초산/초산염 완충용액에서 조사하였다. 한번 사용한 전극은 산 용액으로 처리하여 5회 이상 재사용할 수 있었다. 선형주사 전압전류법을 사용하였을 경우 $2.0{\times}10^{-6}$ M 농도까지 정량이 가능하였다. 시차펄스 전압전류법으로 실험할 경우 $7.0 {\times}10^{-7}$ M 농도까지 직선적으로 감응함을 알 수 있었으며 그 때의 상대 표준편차는 ${\pm}$5.1% 이었다. 이 경우 검출 한계는 $5.O{\times} 10^{-7}$ M이었다. 리간드와 착물을 형성할 것으로 예상되는 여러 금속이온에 대한 방해 작용을 조사하였다. 그 결과 은(I) 이온이 방해를 하지만 염화칼륨으로 사전 처리하여 방해작용을 제거할 수 있었다.

유기산을 이용한 납 요염토양의 복원에 관한 연구

정의덕,강신원,박덕수,신학기,백우현 한국환경과학회 2000 한국환경과학회지 Vol.9 No.5

A study on the removal of Pb ion from Pb-contaminated soil was carried out, using ex-situ extraction process. Tartaric acid (TA) and iminodiacetic acid sodium salt (IDA) as a washing agent were evaluated as a function of concentration, reaction time, mixing ratio of washing agent and recycling of washing agent. TA showed a better extraction performance than IDA. The optimum washing condition of TA and IDA were in the ratio of 1 : 15 and 1 : 20 between soil and acid solution during 1 hr reaction. The total concentrations of Pb ion by TA and IDA at three repeated extraction, were 368.8 ppm and 267.5 ppm, respectively. The recovery of Pb ion from washing solution was achieved by adding calcium hydroxide and sodium sulfide, form the precipitation of lead hydroxide and lead sulfide, and optimum amounts of sodium sulfide and calcium hydroxide were 7 g/ℓ for the TA washing solution and 4 g/ℓ , 5 g/ℓ for the IDA washing solution, respectively. The efficiency of recycle for TA and IDA washing solution were 78.8%, 95.1% and 89.2%, 96.6%, at third extractions under Na_2S and Ca(OH)_2, respectively.

황토의 물리적 특성 및 수용액중의 중금속 이온의 흡착 특성에 관한 연구

정의덕,김호성,박경원,백우현 한국환경과학회 1999 한국환경과학회지 Vol.8 No.4

Removal of Cu(Ⅱ), Cr(Ⅱ) and Pb(Ⅲ) ions from aqueous solutions using the adsorption process on the loesses has been investigated. Variations of contact time, pH, adsorption isotherms and selectivity of coexisting ions were experimental parameters. pH of KJ and YIK samples diluted to 1% solution, was rearly the same with each value of pH 5.58 and 5.49, and both samples showed weak acidic properties. From chemical analysis, both samples contain remarkably different amounts of SiO_2, Al_2O_3 and Fe_2O_3. From XRD measurement, quartz was mainly observed in both samples. Kaolinite was also observed, also in both samples, but Feldspar was only observed in KJ sample. Adsorption of metal ions on the loesses were reached at equilibrium by shaking for about 30min. The adsorption of Cr(Ⅲ) ion was higher than that of Cu(Ⅱ) and Pb(Ⅱ) ions. The order of amount adsorbed among the investigated ions was Cr(Ⅲ)>Pb(Ⅱ)>Cu(Ⅱ). In acidic solution, the adsorptivity of loesses was increased as pH increased. The adsorption of Cr(Ⅲ) ion on the loesses were fitted to the Freundlich isotherms. Freundlich constants(l/n) of KJ and YIK loesses were 0.54 and 0.55, respectively.

국내산 황토를 이용한 수용액의 Pb(II), Cu(II), Cr(III) 및 Zn(II) 이온의 흡착 특성

정의덕,김호성,원미숙,윤장희,박경원,백우현 한국환경과학회 1999 한국환경과학회지 Vol.8 No.4

Removal of Pb(Ⅱ), Cu(Ⅱ), Cr(Ⅲ) and Zn(Ⅱ) ions from aqueous solutions using the adsorption process on domestic loess minerals has been investigated. Variations of contact time, pH, adsorption isotherms and selectivity of coexisting ions and leachate were experimental parameters. YDI, YPT and KRT samples diluted in 1% aquous solution which was adjusted pH 10.8, 8.0 and 6.50, respectively. The result of XRD measurement, Quartz was mainly observed in all samples. In the case of KRT sample, Kaolinite, Feldspar, Chlorite consisting of clay minerals shows almost same pattern with YPT samples. Different properties showed from the YDI sample containing Iillite, remarkably.For all the metals, maximum adsorption was observed at 30min ∼ 60min. Adsorption of metal ions on loess minerals were reached an equilibrium by shaking the solution for about 30min. Removal efficiency of Pb(Ⅱ) ion for KRT, YPT and YDI were 84.7%, 92% and 100%, respectively. The Cu(Ⅱ) and Zn(Ⅱ) adsorptivity on KRT showed the low in various pH solution However, those on YPT and YDI were high than 90% except for the pH 2 solution. The orders of adsorptivities for domestic loess minerals showed as following : YPT>KRT>YDI. The adsorption isotherms of Cu(Ⅱ) and Zn(Ⅱ) ions on clay minerals were fitted to a Freundlich's. Freundlich constants(1/n) of KRT and YPT domestic loess minerals were 0.63, 0.97 and 0.36, 0.25, respectively.

리튬 이온 2차전지의 전극재료의 개발 동향 및 특성

정의덕,박덕수,심윤보 한국에너지학회 1994 에너지공학 Vol.3 No.2