• 소성∙가공
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• 제15권9호
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• pp.667-672
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• 2006

Agglutination is one of the most commonly employed reactions in clinical diagnosis. In this paper, we have designed and fabricated nickel mold insert for injection molding of a microfluidic lab-on-a-chip for the purpose of the efficient detection of agglutination. In the presented microfluidic lab-on-a-chip, two inlets for sample blood and reagent, flow guiding microchannels, improved serpentine laminating micromixer(ISLM) and reaction microwells are fully integrated. The ISLM, recently developed by our group, can highly improve mixing of the sample blood and reagent in the microchannel, thereby enhancing reaction of agglutinogens and agglutinins. The reaction microwell was designed to contain large volume of about $25{\mu}l$ of the mixture of sample blood and reagent. The result of agglutination in the reaction microwell could be determined by means of the level of the light transmission. To achieve the cost-effectiveness, the microfluidic lab-on-a-chip was realized by the injection molding of COC(cyclic olefin copolymer) and thermal bonding of two injection molded COC substrates. To define microfeatures in the microfluidic lab-on-a-chip precisely, the nickel mold inserts of lab-on-a-chip for the injection molding were fabricated by combining the UV photolithography with a negative photoresist SU-8 and the nickel electroplating process. The microfluidic lab-on-a-chip developed in this study could be applied to various clinical diagnosis based on agglutination.

• 대한화학회지
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• 제40권1호
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• pp.11-19
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• 1996

에너지기인 azido기($-CH_2N_3$), nitrato기($-CH_2ONO_2$)로 치환된 옥세탄의 단량체를 $BF_3$촉매하의 공중합에 관해서 반경험적인 MINDO/3, MNDO, AM1 그리고 HF/3-21G 방법 등을 사용하여 이론적으로 고찰하였다. 옥세탄 치환제와 $BF_3$ 이분자 착물의 입체적, 정전기적 구조를 이론적으로 설명할 수 있다. 옥세탄의 공중합 성장단계에서 반응성은 옥세탄의 반응중심 탄소의 양전하 크기와 옥세탄 성장단계의 친전자체의 낮은 LUMO에너지에 좌우됨이 예측된다. 옥세탄의 공중합 반응성비는 계산치와 실험값이 일치하는 랜덤 공중합 반응이다. 평형상태의 고리형 oxonium 이온과 열린 carbenium 이온의 농도 크기가 반응 메카니즘의 결정단계이며, 형태와 계산을 기초로하여 빠른 평형을 예상하여 볼 때 선폴리머 성장단계에서 $S_N1$ 메카니즘이 $S_N2$ 메카니즘보다 빠르게 반응할 것으로 예측된다.

• Bulletin of the Korean Chemical Society
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• 제26권4호
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• pp.641-644
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• 2005

Nucleophilic addition reactions of benzylamines $(XC_6H_4CH_2NH_2)\;to\;{\beta}$-cyanostilbenes ($YC_6H_4CH=C(CN)C_6H_4$Y’) have been studied in acetonitrile at 30.0 oC. A greater degree of N-$C_{\alpha}$ bond formation (larger ${\beta}_X$) is obtained with a stronger electron-withdrawing substituent in either ${\alpha}-\;(\delta\sigma_Y\;{\gt}\;0)\;or\;{\beta}-ring\;(\delta\sigma_{Y'}\;{\gt}$ 0). A stronger charge development is observed in the TS on $C_{\beta}\;(\rho_{Y'}$= 1.06 for X=Y=H) rather than on $C_{\alpha}\;(\rho_{Y}$ = 0.62 for X=Y’H) indicating the lag in the resonance development into the activating group (CN) on $C_{\beta}$ in the transition state. Similarly, the magnitude of $\rho$$_{XY'}$(−0.72) is greater than $\rho_{XY}$ (−0.66) due to a stronger interaction of the nucleophile with $\beta$-ring than $\alpha$-ring. The positive sign of $\rho_{YY'}$correctly reflects $\pi$ bond cleavage between the two rings in the TS. Relatively large kinetic isotope effects ($k_H/k_D\;{\geq}$ 2.0) involving deuterated nucleophiles ($XC_6H_4CH_2ND_2$) suggest a four-membered cyclic TS in which concurrent N-C$_{\alpha}$ and H(D)-C$_{\beta}$ bond formation occurs.

• 한국강구조학회 논문집
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• 제28권6호
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• pp.415-425
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• 2016

스틸스터드 내력벽 시스템은 국외에서 중고층형 모듈러 건축에 널리 사용되는 구조형식이다. 국내의 중고층형 모듈러 시스템에 스틸 스터드 벽체를 적용하기 위해서는 내진성능 확보가 필수적이다. 본 연구에서는 스트랩브레이스를 갖는 모듈러 건축 스틸스터드 내력벽 시스템의 횡력저항성능 및 유효강성을 제안하였다. 스트랩 브레이스와 수직외측스터드의 사양을 달리하는 2개의 실물 실험체에 대해 주기하중에 대한 실험을 실시하여 제안된 설계식을 검증하였다. 수직외측스터드의 휨거동을 고려할 수 있는 설계식을 통해 실험체의 공칭강도, 탄성강성, 항복변위 등을 예측하고 실험을 통해 검증하였다. 실험에 의한 최대강도는 예측식 대비 1.11~1.18배 수준으로 평가되었다. 박판의 스트랩 브레이스를 갖는 스트랩 스터드패널은 일반적으로 에너지소산능력이 매우 낮은 것으로 평가되나, 본 연구에서 제안한 수직외측스터드의 유효높이를 줄이고 브레이스의 각도를 낮춘 시스템의 경우 등가점성감쇠비가 최대 9.42% 수준으로 충분한 에너지소산능력이 확보될 수 있음을 확인하였다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2004년도 추계학술대회 논문집 Vol.17
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• pp.452-455
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• 2004

In this paper, investigations of the SAMs(self-assembled monolayers) of a thiol-fuctionalized viologen derivatives, $V_8SH$ and $SH_8V_8SH$, where, V is N,N'-dialkylbipyridinium (i.e. a viologen group), have been carried out by elucidate voltammetry date. The redox reactions are highly reversible and can be cycled many times without significant side reaction, which has been known as a nano-gram order mass detector through resonant frequency change self-assembly process of the viologen has been investigated with $QCM({\Delta}F)$. The assembling process of the $V_8SH$ and $SH_8V_8SH$ monolayers can be finished completely in about 1 hour. The measured frequency shift for $V_8SH$ and $SH_8V_8SH$ were about 351 and 172 Hz, respectively. From these values, we calculated that the mass adsorbed $V_8SH$ and $SH_8V_8SH$ were about 375 and 183 ng. We believe that this mass loss is caused by the simultaneous loss of the anions present within the monolayer for charge compensation of the viologen dications and some solvent.

• 전기화학회지
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• 제10권2호
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• pp.150-154
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• 2007

본 연구에서는 8족 금속 원소인 오스뮴을 중심금속으로 일차아민을 포함하고 있는 피리딘 (pyridine) 화합물을 배위시켜 착화합물을 합성하였다. 합성된 오스뮴 착화합물은 $[Os(dme-bpy)_2(ap-im)Cl]^{+/2+}$을 순환전압전류법을 포함한 다양한 전기화학분석법을 이용하여 전기적인 성질을 조사하였다. 또한 합성된 일차 아민을 갖는 오스뮴 착화합물을 이용하여 당 측정용 바이오센서를 제작하기 위하여 금 나노입자(Cold nano-particles)를 전기적 흡착방법을 이용하여 스크린 인쇄방법으로 만든 탄소반죽 전극 (Screen Printed Carbon Electrodes, SPEs) 위에 고정화를 시켰다. 당과 당 분해효소(Glucose Oxidase, GOx)를 혼합하여 발생하는 산화촉매전류를 확인하였고, 당 농도에 따라 변화하는 산화촉매전류의 양도 확인하였다. 새롭게 만들어진 바이오센서는 1 mM 과 같은 낮은 농도에서 감응할 수 있는 바이오센서에 응용할 수 있음을 확인하였다.

• 전기화학회지
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• 제12권1호
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• pp.54-60
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• 2009

The redox characteristics of 2-arylaldehydehydrazono-3-phenyl-5-substituted-2, 3-dihydro-1, 3, 4-thiadiazoles (1a-h) have been investigated in nonaqueous solvents such as 1, 2-dichloroethane (DCE), dichloromethane (DCM), acetonitrile (AN), Tetrahydrofuran (THF), and dimethylsulfoxide (DMSO) at platinum electrode. Through controlled potential electrolysis, the oxidation and reduction products of the investigated compounds had been separated and indentified. The redox mechanism had been suggested and proved. It had been found that all the investigated compounds were oxidized in two irreversible one-electron processes following the well-known pattern of The EC-mechanism; the first electron loss gives the corresponding cation-radical which is followed by proton removal from the ortho-position in the N-phenyl ring forming the radical. The obtained radical undergoes a second electron uptake from the nitrogen in the N = C group forming the unstable intermediate (di-radical cation) which undergoes ring closure forming the corresponding cation. The formed cation was stabilized in solution through its combination with a perchlorate anion from the medium. On the other hand, these compounds are reduced in a single two-electron process or in a successive two one-electron processes following the well known pattern of the EEC-mechanism according to the nature of the substituent; the first one gives the anion-radical followed by a second electron reduction to give the dianion which is basic enough to abstract protons from the media to saturate the (C = O) bond.

• 한국수소및신에너지학회논문집
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• 제21권1호
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• pp.50-57
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• 2010

Stepwise production of syn-gas and hydrogen from methane on ferrite based media added with yttria-stabilized zirconia (YSZ) was carried out using a fixed bed infrared reactor. In this study, all M-ferrite (M=Co, Cu, Mn and Ni) media were prepared by co-precipitation method, and there the YSZ was added as a binder to improve thermal stability, reactivity, and resistance against carbon deposition. Most of the ferrite media containing YSZ showed the good redox property for temperature programmed reduction/oxidation (TPR/O) tests. Notably, the Cu-substituted ferrite medium with YSZ showed the great resistance against carbon deposition as well as the good reactivity for the stepwise production of syngas and hydrogen. Furthermore, it also showed the good durability without significant deactivation during five repeated cyclic tests.

• 분석과학
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• 제15권4호
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• pp.388-391
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• 2002

전기화학적 방법으로 콩기름의 산패에 대한 연구를 하였다. 콩기름은 비가역적 전극반응을 하였다. 주사속도를 빠르게 함에 따라, 콩기름의 산화봉우리전위는 음의 방향으로 이동하였고, 그 봉우리전류는 증가했다. 42일까지 대기중의 실내온도에서 방치한 콩기름의 봉우리전위는 거의 변화를 보이지 않았고, 그 이상 방치 후에는 봉우리전위가 큰 폭으로 음의 방향으로 이동했다. 42일까지 방치한 콩기름의 산화봉우리전류는 점차 감소하다가, 그 이상 방치 후에는 봉우리전류가 갑작스럽게 증가했다. 42일 이상 방치 후의 봉우리전류의 증가는 콩기름의 산패에 따른 카보닐작용기의 형성 때문이다.

• 한국수정란이식학회지
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• 제27권3호
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• pp.163-169
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• 2012

The 3-isobutyl-1-methylxanthine (IBMX) is non-selective phosphodiesterase and is able to prevent resumption of meiosis by maintaining elevated cyclic AMP (cAMP) concentrations in the oocyte. The present study was conducted to analyze: (1) nuclear maturation (examined by the Hoechst staining), (2) whether cytoplasmic maturation (examined by the intracellular glutathione (GSH) concentration) of porcine oocytes is improved during meiotic arrest after prematuration (22 h) with IBMX. Before in vitro maturation (IVM), oocytes were treated with 1 mM IBMX for 22 h. After 22 h of pre-maturation, the higher rate of IBMX treated group oocytes were arrested at the germinal vesicle (GV) stage (42.3%) than control IVM oocytes (10.1%). It appears that the effect of IBMX on the resumption of meiosis has shown clearly. In the end of IVM, the reversibility of the IBMX effect on the nuclear maturation has been corroborated in this study by the high proportions of MII stage oocytes (72.5%) reached after 44 h of IVM following the 22 h of inhibition. However, intracellular GSH concentrations were lower in the oocytes treated with IBMX than the control oocytes (6.78 and 12.94 pmol/oocyte, respectively). These results demonstrate that cytoplasmic maturation in porcine oocytes pre-treated with IBMX for 22 h did not equal that of control oocytes in the current IVM system. These results indicate that pre-maturation with IBMX for 22 h may not be beneficial in porcine IVM system.