• 자원환경지질
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• 제52권5호
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• pp.323-336
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• 2019

한반도에서 중생대 화성활동은 주로 트라이아스기 후-충돌대형, 쥐라기 조산대형 그리고 후기 백악기 후-조산대형 화성활동으로 대표되며, 각 지질시대별 광화작용의 다양성은 마그마의 지화학적 특성과 함께 정치 심도의 차별성에서 유도된 서로 다른 지열수계로부터 발생하게 되었다. 백악기 금속광화작용은 후-조산대형 천부 화성활동과 관련된 약 115~45 Ma(주 광화기; 약 100~60 Ma)의 광범위한 기간에 걸쳐서 진행되었으며, 대부분 금속광상은 소규모 암주형 화강암체를 따라 집중되는 공간적 배태양상을 보인다. 경기육괴와 영남육괴에서 후기 백악기 금속광상은 전반적으로 공주-음성 단층계와 영동-광주 단층계 및 경상분지의 경계부를 따라 분포하며, 대부분 원지성 천열수~중열수 Au-Ag 맥상 광상 또는 점이성 중열수 Zn-Pb-Cu 맥상 광상으로 산출되고 있다. 반면에 태백산분지, 옥천대 및 경상분지에서는 스카른형, 탄산염교대형, 열수충진형 맥상, 반암형, 각력 파이프형, 칼린형 광상과 같은 다양한 광상 유형으로부터 상이한 금속종이 산출되고 있다. 후기 백악기 금속광화작용은 지역에 따라 광화유체의 유동성 차이뿐만 아니라, 관계 화강암의 근접성 차이에서 나타나는 침전 환경의 차별성으로부터 다양한 광상유형 및 광종이 유도되었다. 백악기 광상 유형의 다양성은 근본적으로 관계화성암의 분화도 및 산화도와 같은 지화학적 특성에 따라 좌우되지만, 광화유체는 전반적으로 중간황형~저황형(intermediate~low sulfidation) 열수의 진화 특성을 보인다.

• 한국정보전자통신기술학회논문지
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• 제14권3호
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• pp.201-207
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• 2021

머신러닝의 한 종류인 딥러닝은 각 학습 과정을 진행할 때, 가중치를 변경하면서 학습을 수행한다. 딥러닝을 수행할때 대표적으로 사용되는 Tensor Flow나 Keras의 경우 학습이 종료된 결과를 그래프 형태로 제공한다. 이에 과다학습으로 인한 퇴화 현상 또는 가중치의 잘못된 설정으로 인해 학습 결과에 오류가 발생하는 경우, 해당 학습 결과를 폐기해야한다. 이에 기존 기술은 학습 결과를 롤백하는 기능을 제공하고 있지만, 롤백 기능은 최대 5회 이내의 결과로 제한된다. 또한, 딥러닝의 모든 과정을 기록하고 있는 것이 아니기 때문에 값을 추적하기 어렵다. 이를 해결하기 위해 MLOps의 개념을 적용한 기술이 존재하지만. 해당 기술에서는 이전 시점으로 롤백하는 기능을 제공하지 않는다. 본 논문에서는 기존 기술의 문제점을 해결하기 위해 학습 과정의 중간 값을 블록체인으로 관리하여 학습 중간 과정을 기록하고, 오류가 발생할 경우 롤백할 수 있는 시스템을 구성한다. 블록체인의 기능 수행을 위해서 딥러닝 과정 및 학습 결과 롤백은 Smart Contract를 작성하여 동작하도록 설계하였다. 성능평가는 기존의 딥러닝 방식의 롤백 기능을 평가하였을 때, 제안방식은 100%의 복구율을 가지는 것에 비교하여 기존 기법에서는 6회 이후에 복구율이 감소되어 50회일 때 10%까지 감소하는 것을 확인하였다. 또한, 이더리움 블록체인의 Smart Contract를 사용할 때, 블록 1회 생성 시 157만원의 금액이 지속적으로 소모되는 것을 확인하였다.

• 한국건설순환자원학회논문집
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• 제11권1호
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• pp.16-24
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• 2023

미연탄을 사용하는 화력발전소에서 발생되는 석탄재는 Si, Al, Fe 성분을 포함하고 있으며, 이들 성분은 시멘트 클링커에 제조에 필요한 주요성분이다. 특히 Al, Fe 성분은 시멘트 클링커의 간극상을 형성하는 성분으로 시멘트 클링커의 소성에 중요한 영향을 미친다. 본 연구에서는 시멘트 클링커의 원료로서 다량의 석탄재를 함량별로 적용하여, 석탄재를 적용한 시멘트 클링커의 소성온도별 광물형성 과정을 확인하고자 하였다. 석탄재를 다량 적용한 시멘트 클링커는 1050~1150 ℃의 소성온도 구간에서 중간상이 생성되는 것을 확인하였고, 이는 석탄재의 함량이 증가할수록 생성량이 증가하였다. 석탄재의 첨가로 생성된 상은 1350 ℃ 이상에서 칼슘실리케아트상과 간극상으로 전환되어 소멸되는 것으로 예상된다. 시멘트 클링커의 일반적인 소성온도인 1450 ℃에서는 다량의 석탄재를 적용한 시멘트 클링커는 순수원료를 사용하여 제조한 기준 시멘트 클링커와 동등수준의 잘 발달된 광물을 형성하였다.

• Natural Product Sciences
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• 제5권2호
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• pp.80-84
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• 1999

Peroxynitrite is a cytotoxic intermediate produced by the reaction between the superoxide anion radical and nitric oxide. Flavonoids (afzelin, quercitrin and quercetin 3-O-sambubioside), and chlorogenic acid and its methyl ester obtained from leaves of loquat (Eriobotrya japonica) have recently been shown to scavenge 1,1-diphenyl-2-picrylhydrazyl radical and to inhibit lipid peroxidation in mouse liver homogenate. The aim of this study is to investigate the inhibitory effects of the above components on peroxynitrite produced stimulated by 3-morpholinosydnonimine (SIN-1) to produce superoxide anion radical and nitric oxide at the same time. In addition, the present study tests whether or not the components directly scavenge peroxynitrite itself. The results showed that the components with the aromatic ortho-dihydroxyl groups (catechol) were more potent inhibitors of peroxynitrite formation by SIN-1. In particular, the methyl ester form of chlorogenic acid showed the most potent inhibition. At $5\;{\mu}M$ concentration, the order of minimizing peroxynitrite formation were : methyl chlorogenic acid > quercitrin > quercetin 3-O-sambubioside > chlorogenic acid > afzelin. Authentic peroxynitrite was directly scavenged by the components in a manner similar to peroxynitrite formation by SIN-1. In particular, when compared with penicillamine as a positive control, methyl chlorogenate was as effective in inhibiting peroxynitrite formation and approximately 2 times more effective in scavenging an authentic peroxynitrite. These results demonstrate therefore, that components extracted from the leaves of Eriobotrya japonica effectively scavenged peroxynitrite.

• Journal of Photoscience
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• 제9권2호
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• pp.311-313
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• 2002

X-ray structures of pharaonis phoborhodopsin (ppR) show the different direction of the side chain of Arg72 from that of the corresponding residue (Arg82) of bacteriorhodopsin, BR. For BR, this residue is considered to play an important role in the proton pumping. In order to investigate the role of Arg72 in ppR, we constructed Arg72 mutants of R72A, R72K and R72Q, and measured the photocycle and proton pumping activities. The pH-titration curves on the absorption maximum of the mutants were shifted to alkaline in comparison of that of the wild-type. This may imply the increase of pKa of D75, suggesting the presence of the (probably electric) interaction between D75 and Arg72. Rate constants of the M-decay were 3-7 times faster than that of the wild-type, and the time for the completion of the photocycling was also reduced. Using Sn0$_2$ electrode, the rate of transmembrane proton transport was measured upon illumination. The photo-induced proton pumping activities were estimated after the corrections that are the percentages of the associated form of D75 (which has no pumping activity) and the photocycling rates. R72A and R72Q showed the reduced activity while R72K did not reduce the activity.

• Journal of Microbiology and Biotechnology
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• 제18권3호
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• pp.552-559
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• 2008

Ethyl (S)-4-chloro-3-hydroxybutyrate is an intermediate for the synthesis of Atorvastatin, a chiral drug used for hypercholesterolemia. A Rhodococcus erythropolisstrain (No.7) able to convert 4-chloro-3-hydroxybutyronitrile into 4-chloro-3-hydroxybutyric acid has recently been isolated from soil. This activity has been regarded as having been caused by the successive actions of the nitrile hydratase and amidase. In this instance, the corresponding amidase gene was cloned from the R. erythropolis strain and expressed in Escherichia coli cells. A soluble active form of amidase enzyme was obtained at $18^{\circ}C$. The Ni column-purified recombinant amidase was found to have a specific activity of 3.89 U/mg toward the substrate isobutyramide. The amidase was found to exhibit a higher degree of activity when used with mid-chain substrates than with short-chain ones. Put differently, amongst the various amides tested, isobutyramide and butyramide were found to be hydrolyzed the most rapidly. In addition to amidase activity, the enzyme was found to exhibit acyltransferase activity when hydroxyl amine was present. This dual activity has also been observed in other enzymes belonging to the same amidase group (E.C. 3.5.1.4). Moreover, the purified enzyme was proven to be able to enantioselectively hydrolyze 4-chloro-3-hydroxybutyramide into the corresponding acid. The e.e. value was measured to be 52% when the conversion yield was 57%. Although this e.e. value is low for direct commercial use, molecular evolution could eventually result in this amidase being used as a biocatalyst for the production of ethyl (S)-4-chloro-3-hydroxybutyrate.

• 대한화학회지
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• 제20권1호
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• pp.48-55
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• 1976

N-(2,4-dinitrophenyl)-benzimidoyl chloride의 여러가지 유도체의 가수분해 속도상수를 측정하여 넓은 pH 범위에서 잘 맞는 반응속도식을 구하였다. 이 식에 의하면 아직 잘 알려져 있지 않은 산성과 염기성 용액속에서 가수분해 반응메카니즘을 정량적으로 잘 설명할 수 있었다. 즉 pH 7.0 이하에서는 carbonium ion 중간체를 거쳐 반응이 진행되는 $S_n1$ 반응과정이며, pH 8.5 이상에서는 hydroxide ion과 imidoyl chloride 농도에 비례하는 $S_n2$ 반응메카니즘에 의해 가수분해가 진행되며, pH 7.0∼8.5 사이에서는 이 두 반응이 경쟁적으로 일어남을 알았다.

• 자원환경지질
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• 제27권2호
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• pp.161-170
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• 1994

Jindong Granites are plotted mainly in the region of granodiorite~diorite of the Streckeisen's diagram, while Yucheon-Eonyang Granites and Onjonri Granites in the region of monzo-granite and monzo-granite~granodiorite, respectively. Jindong Granites show a differenciation trend of calc-alkaline magma, and its magmatic evolution from intermediate to acidic rocks, which might form mineralizing solution, is consistant with the general path of the Cretaceous granitic rocks including Yucheon-Eonyang Granites and Onjongri Granites. The differenciation index (D.I.) is 35~80 for Jindong Granites, which is lower than 85~95 of Yucheon-Eonyang Granites and is partly overlapped by 67~84 of Onjongri Granites. There is clear difference in content of some major and trace elements between Jindong Granites of Cu province and the other granitic rocks of Pb-Zn and Mo provinces. Between these metallogenic provicnes, Cu content is high in Jindong Granites near Haman-Gunbuk mineralized zone, while Pb and Zn are relatively abundant in Yucheon-Eonyang Granites and Mo in Onjongri Granites. Therefore, Jindong Granites of the Cu province are distinguishable by chemical compositions and their related geochemical characteristics from the other Cretaceous granitic rocks of Pb-Zn and Mo provinces. However, the content of Cu and Cl in biotite is applicable to distinguish a productive phase from a barren phase of Jindong Granites, because Cu and Cl show a trend to be concentrated in biotite of Jindong Gratites in the Haman-Gunbuk mineralized zone.

• Bulletin of the Korean Chemical Society
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• 제33권8호
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• pp.2719-2723
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• 2012

A kinetic study is reported for nucleophilic substitution reactions of benzyl 4-pyridyl carbonate 6 with a series of alicyclic secondary amines in MeCN. The plot of pseudo-first-order rate constant ($k_{obsd}$) vs. [amine] curves upward, which is typical for reactions reported previously to proceed through a stepwise mechanism with two intermediates (i.e., a zwitterionic tetrahedral intermediate $T^{\pm}$ and its deprotonated form $T^-$). Dissection of $k_{obsd}$ into the second- and third-order rate constants (i.e., $Kk_2$ and $Kk_3$, respectively) reveals that $Kk_3$ is significantly larger than $Kk_2$, indicating that the reactions proceed mainly through the deprotonation pathway (i.e., the $k_3$ process) in a high [amine] region. This contrasts to the recent report that the corresponding aminolysis of benzyl 2-pyridyl carbonate 5 proceeds through a forced concerted mechanism. An intramolecular H-bonding interaction was suggested to force the reactions of 5 to proceed through a concerted mechanism, since it could accelerate the rate of leaving-group expulsion (i.e., an increase in $k_2$). However, such H-bonding interaction, which could increase $k_2$, is structurally impossible for the reactions of 6. Thus, presence or absence of an intramolecular H-bonding interaction has been suggested to be responsible for the contrasting reaction mechanisms (i.e., a forced concerted mechanism for the reaction of 5 vs. a stepwise mechanism with $T^{\pm}$ and $T^-$ as intermediates for that of 6).

• Bulletin of the Korean Chemical Society
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• 제33권9호
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• pp.2971-2975
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• 2012

Second-order rate constants $k_N$ have been measured spectrophotometrically for nucleophilic substitution reactions of t-butyl 4-pyridyl carbonate 8 with a series of alicyclic secondary amines in $H_2O$ at $25.0{\pm}0.1^{\circ}C$. The Br${\emptyset}$nsted-type plot for the reactions of 8 is linear with ${\beta}_{nuc}$ = 0.84. The ${\beta}_{nuc}$ value obtained for the reactions of 8 is much larger than that reported for the corresponding reactions of t-butyl 2-pyridyl carbonate 6 (i.e., ${\beta}_{nuc}$ = 0.44), which was proposed to proceed through a forced concerted mechanism. Thus, the aminolysis of 8 has been concluded to proceed through a stepwise mechanism with a zwitterionic tetrahedral intermediate $T^{\pm}$, in which expulsion of the leaving-group from $T^{\pm}$ occurs at the rate-determining step (RDS). In contrast, aminolysis of benzyl 4-pyridyl carbonate 7 has been reported to proceed through two intermediates, $T^{\pm}$ and its deprotonated form $T^-$ on the basis of the fact that the plots of pseudo-first-order rate constant $k_{obsd}$ vs. amine concentration curve upward. The current study has demonstrated convincingly that the nature of the leaving and nonleaving groups governs the reaction mechanism. The contrasting reaction mechanisms have been rationalized in terms of an intramolecular H-bonding interaction, steric acceleration, and steric inhibition.