• 한국식품과학회지
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• 제1권1호
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• pp.45-50
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• 1969

자외부흡광 스펙트럼의 변화와 티 비 에이(TBA) 반응으로 살필 때, 수용액의 송에서의 말론알데하이드(malonaldehyde)는 과장 $260m/{\mu}$ 부근의 자외선조명에 의하여 광화학적 변화를 받는다. 이 용액에 아프라톡신(aflatoxin) 을 가하면 파장 $360m/{\mu}$ 부근의 광선에 의해서 이와 같은 변화가 재빨리 일어나며, 또 보통 형광등을 이용한 실험실의 조명에 의해서도 비록 그 변화는 느려지지만 마찬가지로 일어난다. 이과 같은 변화는 비가역적이며, 이 반응에서 아프라톡신은 다만 감광제로서의 역할을 한다. 또 이 반응의 기작은 말론알데하이드 분자의 평행적 이중결합체 형성에 의한 것 같다.

• 한국재료학회지
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• 제33권7호
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• pp.315-322
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• 2023

In the present work, we address the new route for the green synthesis of manganese dioxide (MnO₂) by an innovative method named the solution plasma process (SPP). The reaction mechanism of both colloidal and nanostructured MnO₂ was investigated. Firstly, colloidal MnO₂ was synthesized by plasma discharging in KMnO₄ aqueous solution without any additives such as reducing agents, acids, or base chemicals. As a function of the discharge time, the purple color solution of MnO₄^- (oxidation state +7) was changed to the brown color of MnO₂ (oxidation state +4) and then light yellow of Mn²⁺ (oxidation state +2). Based on the UV-vis analysis we found the optimal discharging time for the synthesis of stable colloidal MnO₂ and also reaction mechanism was verified by optical emission spectroscopy (OES) analysis. Secondly, MnO₂ nanoparticles were synthesized by SPP with a small amount of reducing sugar. The precipitation of brown color was observed after 8 min of plasma discharge and then completely separated into colorless solution and precipitation. It was confirmed layered type of nanoporous birnessite-MnO₂ by X-ray powder diffraction (XRD), fourier-transform infrared spectroscopy (FT-IR), and electron microscopes. The most important merits of this approach are environmentally friendly process within a short time compared to the conventional method. Moreover, the morphology and the microstructure could be controllable by discharge conditions for the appropriate potential applications, such as secondary batteries, supercapacitors, adsorbents, and catalysts.

• 한국분말재료학회지
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• 제13권5호
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• pp.305-312
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• 2006

Amorphous carbon nanotubes were synthesized by a reaction of benzene, ferrocene and Na mixture in a small autoclave at temperatures as low as $400^{\circ}C$. The resulting carbon nanotubes were short and straight, but their inner hole was filled with residual products. The addition of quartz to the reacting mixture considerably promoted the formation of carbon nanotubes. A careful examination of powder structure suggested that the nanotubes in this process were mainly formed by surface diffusion of carbon atoms at the surface of solid catalytic particles, not by VLS(vapor-liquid-solid) mechanism.

• 한국수산과학회지
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• 제22권6호
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• pp.391-396
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• 1990

Changes in electric resistance was measured to carry out the kinetic analysis of milk gellation upon addition of rennet. Using pasteurized milk and commercial rennin, kinetic properties were investigated during milk gellation in terms of initial hydrolysis and coagulation steps. Specially designed reactor with two platinum electrodes was used throughout the experiments. As a function of either milk concentrations or reaction temperatures, gel time exhibited directly proportional relations: on the contrary, gel time was inversely pro-portional to enzyme concentration. Activation energies for enzymatic degradation and cogulation were 16.3, 4.6 and 34, 8.6 Kcal/mol, repectively. This simple analytical method proved to be very effective to characterize the mechanism of milk gellation. Moreover, unlike other methods, this method reguired simple apparatus and short time of analysis.

• 환경위생공학
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• 제13권3호
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• pp.141-147
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• 1998

Under high temperature and high pressure, cyanogen disinter gration distruction mechanism brought followings results through continuous plug flow reactor system. 1. The temperature was a important reacting factor in cyanogen disintegration. Over $612.8^{\cird}K$ high disintegration rate or 99.99% was shown even under $2000{\;}mg/{\ell}$ cyanogen density. 2. The conditions of cyanogen disintegration was gained through experimenting the supercrietical condition of water in basic. To gain 99.99% disintegration rate under $1000{\;}mg/{\ell}$ early cyanogen density, the pressure showed 52.8 seconds at $523^{\cird}K$ and 84.2 atm and gained $0.56{\;}mg/{\ell}$ operating density. 3. Here is the reaction velocity formula of cyanogen disintegration by hydrolysis: This formula indicates the high possibility of cyanogen disintegration within a short time. And it also implys the potential possibility on treating NBDICOD and the technology in developing the environment cleaning progress as small size automatic controlling equipment.

• Bulletin of the Korean Chemical Society
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• 제17권11호
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• pp.1023-1031
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• 1996

A new synthetic route for the lanthanum β-diketonate compounds via in-situ formed lanthanum alkyl complexes was developed in the process for the development of suitable MOCVD (metal-organic chemical vapor deposition) precursors of PLT, one of the promising material for the ferroelectric film. A series of lanthanum β-diketonate compounds were successfully synthesized by this method. This new method is found to have some merits; versatile method for almost every β-diketone, β-hydroxyketone, and β-hydroxyaldehyde, short reaction time, easy purification for high purity, moderate to high yield, and easy access to anhydrous compounds. In some cases, anhydrous oligomeric products fail to show the higher volatility. On the other hand, some lanthanum β-diketonates with aromatic groups such as La(1,3-biphenyl-l,3-propandione)3 are found to have favorable properties for a precursor of lanthanum oxide, one of major components of PLT, such as low melting point, and much higher decomposition temperature. A plausible pyrolysis mechanism is proposed by the TGA, where consecutive dissociation of R, CO, CH, C, and O fragments occurs.

• 한국광학회지
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• 제2권4호
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• pp.227-232
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• 1991

The possibility for the high intensity and energy possessing a short pulse in the HF chemical laser system which contained fluoride molecules (RF) was demonstrated theoretically through the numerical model simulation. The calculation was accomplished by assuming that the thermal branched chain mechanism of RF was occurred in the initiation step of $H_2+F_2$ chain reaction. Variations of the major chemicals and the temperature in the system were calculated as a function of time. An analysis was also performed to evaluate output pulse profile through parametric studies.

• 한국연소학회지
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• 제18권4호
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• pp.29-36
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• 2013

Numerical study was conducted to clarify effects of added $CO_2$ for the downstream interaction between $H_2$-air and CO-air premixed flames in counterflow configuration. The reaction mechanism adopted was Davis model which had been known to be well in agreement with reliable experimental data. The results showed that both lean and rich flammable limits were reduced. The most discernible difference between the two with and without having $CO_2$ addition into $H_2$-air and CO-air premixtures was two flammable islands for the former and one island for the latter at high strain flame conditions. Even a small amount of $H_2$, in which $H_2$-air premixed flame cannot be sustained by itself, participates in CO oxidation, thereby altering the CO-oxidation reaction path from the main reaction route $CO+O_2{\rightarrow}CO_2+O$ with a very long chemical time in CO-air flame to the (H, O, OH)-related reaction routes including $CO+OH{\rightarrow}CO_2+H$ with relatively short chemical times. This intrinsic nature alters flame stability maps appreciably. The results also showed that chemical effects of added $CO_2$ suppressed flame stabilization. Particularly this phenomenon was appreciable at flame conditions which lean and rich extinction boundary was merged. The detailed discussion of chemical effects of added $CO_2$ was addressed to the present downstream interaction.

• 한국연소학회지
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• 제20권1호
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• pp.6-14
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• 2015

Numerical study was conducted to clarify effects of added $H_2O$ for the downstream interaction between $H_2$-air and CO-air premixed flames in counterflow configuration. The reaction mechanism adopted was Davis model which had been known to be well in agreement with reliable experimental data. The results showed that both lean and rich flammable limits were reduced in increase of strain rate. The most discernible difference between the two with and without having $H_2O$ and/or $H_2$ addition into $H_2$-air and CO-air premixtures was two flammable islands for the former and one island for the latter at high strain flame conditions. Even a small amount of $H_2$, in which $H_2$-air premixed flame cannot be sustained by itself, participates in CO oxidation, thereby altering the CO-oxidation reaction path from the main reaction route $CO+O_2{\rightarrow}CO_2+O$ with a very long chemical time in CO-air flame to the OH-related reaction routes including $CO+OH{\rightarrow}CO_2+H$ with very short chemical times. This intrinsic nature alters flame stability maps appreciably. The results also showed that chemical effects of added $H_2O$ help lean flames at relatively low strain rate be sustained, and suppress the flame stabilization at high strain rates.

• 한국결정성장학회지
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• 제32권2호
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• pp.68-76
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• 2022

본 연구는 오토클레이브에서 양생된 시편들을 침지했을 때 시편의 압축강도 변화 메커니즘(mechanism) 규명을 위해 수행되었다. 침지는 3일, 7일, 21일간 진행되었으며, 침지 용액은 증류수, 2M, 8M, 14M 알칼리용액에서 진행되었다. 단기간동안 침지한 시편들의 압축강도 변화는 크지 않았으나, 21일 동안 증류수 및 8M 알칼리 용액에 침지한 시편들의 압축강도는 추가적인 지오폴리머 반응에 의해 침지전 시편에 비해 2배 이상 증가하였다. 하지만, 일정농도 이상으로 알칼리를 공급해주면 알칼리 골재 반응에 의해 압축강도가 감소하였다. 따라서 오토클레이브에서 양생한 시편들의 압축강도 증진을 위해서는 증류수 및 8M 알칼리용액에서 21일 이상 장기간 침지하는 것이 바람직한 것으로 판단되었다.