The relative reactivities of branched and linear polycarbonates were investigated by measuring unreacted chloroformate concentration. It was found that the polymerization for the branched polymer proceeded ca. 10 times faster than that for the linear polymers. The effect of catalyst on a condensation step was studied by changing the amount of TEA (triethylamine) at t0 and t60 with keeping constant amount of TEA. The viscosity average molecular weight for the obtained branched polycarbonates were measured and compared with those of linear polycarbonates. It was found that the viscosity molecular weights of the obtained polymers decreased nonlinearly as wt % of added oligomer increased. The solution viscosities in methylenechloride for linear and branched polycarbonate increased nonlinearly as the content of polymer increased.

Diazotization of STA synthesized by the indirect diazotization method. The effect of catalyst and agitation (rpm) about STA and H-acid reaction were examined and the optimum conditions were investigated experimentally. The yields and characteristics of 1.st coupling and diazotization synthesis were identified by HPLC and FT-IR analysis. 1.st condensation of CNC and mPDSA were synthesized at 5℃ and pH=6.5. The conditions of alkaly coupling of H-acid were synthesized at 5℃ and pH=8. The condensation of products was identified by U. V. analysis. From this results, It was obtained to reactive dyestuffs of bi-functional reactivity with high fastness and high adsorption.

The metal complexes containing amino acidic ligands were prepared by using 11 kinds of amino acids as ligands and Ni, Cu, Co, Zn, Fe as a central metal. The starting was continued for 4hrs at room temperature. But Bis(D,L-Serine)Ni (II), and (D,L-Serine)Co (II) were prepared by heating method(80℃). In order to investigated reaction activity of Bis(D,L-Aspartato) Metal(II), stirring time was varied and Bis(D,L-Tyrosine ) Metal(II) used different divalent metal salts. We anticipate getting a great value from these prepared complexes as a monomer and a catalyst of polymerization which has peculier characteristics.

This study is on a seismic analysis of ab50rber rod in KMRR Reactivity Control Mechanism. The model being studied is two coaxial tubes(control absorber rod and flow tube) immersed in the water and partially coupled(overlap) by water gap. The hydrodynamic mass effects by the water in 않ch surrounding conditions are considered in the model. The natural frequencies, stresses and displacements of the system due to Safe Shutdown Earthquake are computed in the cases of in-phase m여es and out-of-phase modes of two coaxial tubes. The results show that maximum stresses are well below the allowable limit but the maximum displacements at the ends of both tu∞s are 50 much that the ab50rber rcxi contacts with the flow tube(or surrounding wall).

대표적인 유기인계 살충성 0,0-diethylphenylphosphate 유도체의 양자 약리학적 특성에 대한 이해를 도모하기 위하여 EHT와 CNDO/2분자궤도 함수 계산방법으로 0,0-diethylphenylphosphate 분자의 형태와 에너지성분 및 반응성을 검토하였다. 형태이성체들에 대한 전체에너지()와 쌍극자 능율값()을 계산한 바, 보다 인 형태가 와 및 만큼 작은 값을 나타낼뿐만 아니라, steric factor도 작아지므로 형태가 가장 알짜 안정화된 형태이었으며 형태에 대한 HOMO, LUMO에너지, 알짜 전하, overlap population, AO계수 등을 계산하였다. Hammett식에 적용하며 치환기 효과를 검토한 결과, 전자를 끄는 치환기에 의하여 P원자의 양하전이 증가하는 coulomb term 효과와 LUMO에너지가 낮아지는 frontier orbital term 효과가 같은 경향으로 이루어저 charge-control-led reaction과 orbital-controlled reaction이 일어나는 형의 반응성을 갖는다는 사실을 알았다.

In this study, the applicability of reduction-oxidation-linked treatment was evaluated for nitrobenzene and a by-product by analyzing the reaction kinetics. Nitrobenzene showed very low reactivity to persulfate that was activated using various methods. Nitrobenzene effectively reacted through the reduction process using Zero-Valent Iron (ZVI). However, aniline, a toxic substance, was produced as a by-product. Reduction-oxidation-linked treatment is a method that can allow the oxidative degradation of aniline after reducing nitrobenzene to aniline. The experimental results show improved reactivity and complete decomposition of the by-product. Improved reactivity and decomposition of the by-product were observed even under conditions in which the reduction-oxidation reaction was induced simultaneously. No activator was injected for persulfate activation in the process of reducing oxidant linkage, and the activation reaction was induced by ferrous iron eluted from the ZVI. This indicates that this method can be implemented relatively simply.

본 연구에서는 콘크리트내로 침투하는 염소이온을 모니터링하기 위하여, 스크린프리트 기법으로 염소이온 반응형 부식센서를 개발하고, 센서의 세선 수가 부식반응도 및 민감도에 미치는 영향을 실험을 통하여 정량적으로 분석하였다. 개발된 부식센서를 이용하여 염소이온량에 따라 부식 반응도을 확인하였으며, 센서의 파괴정도에 따른 저항변화에서는 단선형 센서보다 다선형 센서에서 큰 저항 변화를 나타내었다. 또한, 부식센서는 NaCl 수용액의 농도가 높은 만큼 센서의 저항변화가 크고, 콘크리트 내에서 센서 종류에 따른 부식저항은 단선형보다 다선형에서 민감도가 높게 나타났으며, 센서의 매설깊이가 클수록 저항변화 사이클 (cycle)은 증가하였다. 이상의 결과로, 본 연구에서 개발된 부식센서는 염분에 대한 부식반응과 민감도, 저항의 변화를 감지할 수 있었으며, 특히 7세선이 우수한 결과를 나타내어, 염분의 침투정도를 모니터링 하는데 가장 적합하다고 판단된다.

많은 미생물들이 수용성 망간이온(Mn2+)을 불용성인 산화망간(Mn4+) 광물로 산화 침전시키는데, 이와 같은 생물학적 산화반응은 비생물학적 산화반응보다 훨씬 빠르게 일어난다. 이처럼 미생물에 의해 생성된 바이오 산화망간 광물은 표면의 강한 흡착성과 산화환원 반응을 통해 생지구화학 순환과 환경오염물질의 생물흡수도에 큰 역할을 한다. 본 논평은 양자역학의 밀도범함수 이론에 바탕을 둔 전산모사를 이용하여 산화망간 광물 표면의 독성금속 흡착의 자세한 기작과 망간원자 빈자리의 광화학적 역할을 새롭게 밝힌 최근 연구결과를 소개한다.