• Bulletin of the Korean Chemical Society
• /
• 제23권3호
• /
• pp.395-399
• /
• 2002

The voltammetric behavior of spontaneously adsorbing Mo layers on Pt(111) and Pt(100) electrodes has been studied to estimate the number of electrons involved in the electrochemical processes of spontaneously adsorbed Mo and the number of the bloc ked Pt sites for hydrogen adsorption. On Pt(111) and Pt(100) surfaces, the spontaneously adsorbed Mo layers showed redox peaks at 0.10 V and 0.15 V, respectively, and continuous current-potential waves in the conventional hydrogen region. Since the potential range of the Mo redox processes on both surfaces overlapped partially with the potential range of hydrogen adsorption, the variation in the ratio of the total charge of Mo and H ($Q_H$ +$Q_{MO}$) to the hydrogen charge of clean Pt electrode ($Q_H^0$) was analyzed. From the analysis, six electrons were estimated to be involved in the electrochemical processes of the spontaneously adsorbed Mo, and four Pt sites for hydrogen adsorption were calculated to be blocked by one adsorbed Mo atom. Based on these figures and the pH dependence of the Mo redox processes, we have proposed an electrochemical equation for the spontaneously adsorbed Mo. This electrochemical equation led us to conclude that the saturation coverage of the spontaneously adsorbed Mo is 0.25. The coverage of Mo less than 0.25, however, could not be determined voltammetrically due to the convolution of the charges of Mo and H.

• 콘크리트학회논문집
• /
• 제18권2호
• /
• pp.213-218
• /
• 2006

시멘트페이스트 공극 내 확장 메니스커스 영역을 초승달 영역, 박막 영역, 흡착 영역으로 구분하고 공극 크기에 따른 액막 두께, 흡착층 두께, 모세관 압력, 분리 압력을 압력 평형 방정식을 이용하여 산정하였다. 그 결과 공극 크기와 흡착층 두께와의 연관식을 도출할 수 있었으며, 공극 크기 $1nm{\sim}1{\mu}m$에 따른 흡착층 두께는 $0.299{\sim}2.700nm$로 나타났고 특히 10nm이하의 공극에서 흡착층 두께 감소에 따른 분리압력의 증가효과가 크게 나타났다. 따라서 시멘트페이스트의 자기 수축은 10nm이하의 공극이 생성되면서 크게 증가하는 것으로 판단된다. 이러한 분리 압력과 모세관 압력을 수축 구동력으로 적용한 자기 수축 예측치는 실험값에 비하여 재령 $1{\sim}4$일까지는 작게 이후부터는 큰 결과를 나타내었다. 이는 초기재령에서의 공극측정시 공극 손상과 이에 따른 수축구동력 과소평가와 불포화 개별공극 가정에 따른 수축구동력 과대평가의 상호작용으로 판단되므로 추후 이에 대한 보완점으로 수화도등의 공극 대체 모델과 불포화공극에 대한 고려사항이 필요할 것으로 판단된다.

• 대한의용생체공학회:의공학회지
• /
• 제14권4호
• /
• pp.307-314
• /
• 1993

Plasma protein adsorption is the first event in the blood-material interaction and influenc- es subsequent platelet adhesion towards thlㅈombus formation. Thiㅈomboembolic events are strongly influenced by surface characteristics of materials and fluid dynamics inside the blood pump. In vitro flow visualizaion and an amimal experiment with the moving actuator type TAH were Performed in order to investigate fluid dynamic effects on the protein adsorption. The diffel'encl level, j of shear rate inside the ventricle Lvere determined by consid- ering the direction of the major opening of four healt valves in the implanted TAH and the visualized flow patterns as well. Each ventricle of the explanted TAH was sectionalized into 12 segments according to the shear rate level. The adsorbed protein on each segment was quantified using the ELISA method after soaking in 2% (wye)SDS/PBS for two days. Adsorbed protein layer thicknesses Itvere measured by the Immunogotd method under TEM. The SEM observation show that right ventricle (RV) , immobilized with albumin, displayed different degrees of platelet adhesion on each segment, whereas the left ventricle (LV), grafted by PEO-sulronate, indicated nearly , iame platelet adhesion behavior, regardless of shear rates. The surface concentrations of adsorbed proteins in the low shear rate region are hlghel'than those in the high region, which was confirmed statistically. A modified adsorption model of plasma protein onto polyurethane surface was suggested by considering the effect of the fluid dynamic characteristics.

• Bulletin of the Korean Chemical Society
• /
• 제35권9호
• /
• pp.2749-2752
• /
• 2014

Recent studies have shown that single-stranded DNA adsorbed onto graphene oxide is protected from DNase I cleavage. However, double-stranded DNA bound to graphene oxide and could be digested by DNase I. To elucidate whether single-stranded DNA is protect from DNase I in the presence of graphene oxide, this study conducted DNase I digestion using single-stranded DNA and single-stranded DNA containing the duplex region in the presence of graphene oxide. Addition of DNase I resulted in restoration of the fluorescence emission that had been quenched when DNA was adsorbed to graphene oxide. It indicates that DNase I cleaved the adsorbed single-stranded DNA onto graphene oxide, which was sufficient for the detection of DNase I activity.

• 대한화학회지
• /
• 제22권5호
• /
• pp.289-294
• /
• 1978

흑연과 산화알루미늄(Alucer) 표면에 흡착된 벤젠이나 p-크실렌분자가 submonolayer 영역에서 어떤 흡착상태를 이루고 있는가를 이론적으로 살펴보기 위하여, 이들 흡착질 분자를 2차원 기체와 조화진동자의 두가지 모형으로 가정하고 통계열역학적으로 흡착엔트로피를 계산하여 실험치와 비교하였다. 그 결과 벤젠은 흑연표면에서 조화진동 운동을 하며, 산화알루미늄 표면에서는 비편재된 상태에 있다는 것을 알게 되었다. 흡착제 표면에서 흡착된 분자가 조화진동 운동을 한다고 가정할 경우 조절가능한 파라미터로 도입된 분자진동수는 $10^{11}\;sec^{-1}$로서 대단히 합리적인 값을 얻었다. p-크실렌분자가 흑연이나 산화알루미늄 표면에 흡착될 때는 단분자층이 이루어지기 훨씬 전에 비정상적인 값들이 나타난다.

• 한국진공학회지
• /
• 제15권2호
• /
• pp.139-144
• /
• 2006

Scanning tunneling microscopy (STM)를 이용하여 Si(111)$4{\times}1$-In 표면에의 수소원자 흡착의 영향을 고찰하였다. STM 이미지에서 수소원자는 $4{\times}1$-In chain의 한 쪽 줄에 있는 두개의 연속된 밝은 부분 사이에 위치한다. 이 H 원자는 두 줄의 zigzag subchain 중의 한 쪽에만 선택적으로 흡착되는 경향성을 보이며 이는 수소원자의 흡착에 표면 밑의 구조가 영향을 미침을 시사한다. 표면에 흡착된 수소원자는 흡착위치 주위의 국소적 변형 뿐 만 아니라 chain 방향으로 멀리 떨어진 곳에도 영향을 미쳐서 STM 이미지에 두 배 주기의 modulation이 나타나게 한다. 수소흡착에 의해 유도되는 두 배 주기의 modulation은 기존에 보고된 Na 원자 흡착에 의해 유도되는 상과 다름을 확인하였다.

• 대한의용생체공학회:의공학회지
• /
• 제15권1호
• /
• pp.19-26
• /
• 1994

Sulfonated poly (ethyleneoxide)-grafted polyurethane (PU-PEO-$SO_3$) prepared by bulk modification was coated on a blood sac for electrohydraulic left ventricular assist device (ELVAD) implanted in dogs and its in vivo blood compatibility on shear stress was studied as compared with untreated Po. The effect of the wall shear stress on the protein adsorption unlike platelet adhesion is dependent on the surface characteristics of the material, although less proteins seem to be adsorbed in the region of the high shear stress. The thickness of total proteins adsorbed on PU-PEO-SOJ (400 ${\AA}$) by trans¬mission electron microscopy(TEM) was considerably lower than that of untreated PU(l,000~1,600 ${\AA}$), but PU-PEO-$SO_3$ showed high albumin adsorption, low fibrinogen and IgG adsorption, and low platelet adhesion as compared with untreated PU, suggesting that PU-PEO-$SO_3$ is more in vivo blood compatible. Therefore, it appears that such a blood compatible PU-PEO-$SO_3$ is useful for blood contacting biomaterials including artificial organs.

• 자원환경지질
• /
• 제36권1호
• /
• pp.17-25
• /
• 2003

동명광산을 경유하는 수계의 pH는 5.9∼7.1의 변화를 보여 약산성 내지는 중성의 환경을 보인다. 하천수 중 중금속 원소함량의 분포는 자원소의 지구화학적 특성에 따라 다양한 분포 양상을 보이나 전반적으로 폐광산 주변에서 증가하는 경향을 보인다. 동명광산 지역의 광미, 폐석적치장토양, 농경지토양에 대한 성분분석 결과 농경지토양에는 중금속의 총 농토가 광미나 폐석적치장의 토양보다 훨씬 낮았을 뿐 아니라 총 중금속 농도 중 adsorbed, carbonate, reducible fraction들이 차지하는 비율이 낮아 이들이 농작물이나 주변 수계에 큰 영향을 미치지 못할 것으로 생각된다. 그러나 하천수중 중금속 원소함량 분포가 전반적으로 광산지역에서 증가하는 경향을 보이며, 광미나 폐석적치장 토양에서도 중금속의 총 농도가 매우 높았을 뿐 아니라 adsorbed, carbonate, reducible fractions들이 차지하는 비율이 농경지 보다 상대적으로 높았기 때문에 이들이 유실되거나 또는 산성우, 산성인 광산폐수의 유입 등으로 인해 화학적 환경변화가 발생할 경우 중금속 오염의 확산이 우려되므로 이에 대한 오염방지대책이 필요하다고 생각된다.

• Bulletin of the Korean Chemical Society
• /
• 제13권1호
• /
• pp.30-32
• /
• 1992

The apparent depth of space charge region on the ZnO $(10{\bar{1}}0)$ surface in chemisorption of oxygen has been estimated from the capacitance of two contacting faces. When the sample (donor concentration: $2.4{\times}10^{22}\;m^{-3}$) was evacuated at 773 K for 1 hr the depth reached to 40-100 ${\AA}$ depending on sample assembly. Admission of oxygen to the sample resulted in an increase of the depth to 3600 ${\AA}$ where the increment was greater at higher oxygen pressure between 6.6-1600 $N/m^2$. Admission of CO to the sample previously exposed to oxygen yields a decrease in the depth. The results of the measurement support that oxygen is adsorbed as an acceptor on ZnO $(10{\bar{1}}0)$.

• Bulletin of the Korean Chemical Society
• /
• 제19권7호
• /
• pp.754-760
• /
• 1998

It was found that the adsorption of a cobalt(III) complex with a macrocyclic ligand, C-meso-5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane (hmc), was induced on a glassy carbon electrode by heavily oxidizing the electrode surface. Adsorption properties are discussed. The glassy carbon electrode with the adsorbed complex was employed to see the catalytic activities for the electro-reduction of O2. In the presence of oxygen, reduction of (hmc)Co3+ showed two cathodic waves in cyclic voltammetry. Compared to the edge plane graphite electrode at which two cathodic waves were also observed in a previous study, catalytic reduction of O2 occurred in the potential region of the first wave while it happened in the second wave region with the other electrode. A rotating disk electrode after the same treatment was employed to study the mechanism of the O2 reduction and two-electron reduction of O2 was observed. The difference from the previous results was explained by the different reactivity of the (hmc)CoOOH2+ intermediate, which is produced after the two electron reduction of (hmc)Co3+ in the presence of O2.