• 대한화학회지
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• 제18권3호
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• pp.153-156
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• 1974

황산산성에서의 히드라진과 요오드의 반응에 대하여, 기체발생속도를 측정하였다. 이미 보고된 요오등의 소비속도의 경우와 마찬가지로, 히드라진 및 요오드의 농도에 관하여는 1차 반응이며, 반응속도는 요오드화이온의 농도에 역비례한다. 그뿐만 아니라, 요오드으이 소비속도롸 기체 발생속도가 거의 같으므로, 수명이 긴 중간물이 생기지 않는다고 결론지을 수 있다

• Bulletin of the Korean Chemical Society
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• 제33권4호
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• pp.1231-1234
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• 2012

A one-pot efficient procedure for the synthesis of 2,4,5-triaryl-1H-imidazole derivatives in good to excellent yields by reaction between hexamethyldisilazane and arylaldehydes, benzyl alcohols, benzyl halides in the presence of molecular iodine has been developed. The remarkable advantages of this method are the simple workup procedure, high yields of products, and the availability of reagents.

• Bulletin of the Korean Chemical Society
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• 제1권2호
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• pp.62-68
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• 1980

Ultraviolet spectrophotometric investigations have been carried out the systems of monoalkylbenzene with iodine in carbon tetrachloride. The results reveal the formation of one to one molecular complexes. The equilibrium constants for these complexes of representative monosubstituted benzene reveal the following order of increasing stability: benzene < methyl- < ethyl- < n-propyl-benzene. The value of ${\Delta}H$, ${\Delta}G$, and ${\Delta}S$ for interaction of a number of monoalkyl substituted benzene with iodine has been determinated. In general, as ΛH becomes increasingly negative, corresponding decreases in ${\Delta}G$ and ${\Delta}S$ values are observed, and these variation are linear. The thermodynamic constants become increasingly negative with increasing monoalkyl substitution of the aromatic donor nucleus. The complex bond is therefore weak, and its formation is accompanied by relatively small entropy changes.

• 한국원자력학회:학술대회논문집
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• 한국원자력학회 2004년도 추계학술발표회 발표논문집
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• pp.461-462
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• 2004

• 한국원자력학회:학술대회논문집
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• 한국원자력학회 2005년도 추계학술발표회
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• pp.677-678
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• 2005

• 대한화학회지
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• 제25권4호
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• pp.228-235
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• 1981

피리딘, ${\beta}$-피코린 및 3,5-루티딘과 요오드사이에 형성되는 전하이동착물을 사염화탄소 용액에서 자외선분광광도법을 사용하여 연구한 결과 $C_5H_5N{\cdot}I_2$, ${\beta}-C_5H_4(CH_3)N{\cdot}I_2$ 및 3,5-$C_5H_3(CH_3)_2N{\cdot}I_2$ 형의 1:1 분자착물이 형성됨을 알았다. 이들 착물생성에 대한 흡수최대는 온도가 상승함에 따라 blue shift되므로 이를 고려하여 각 온도에서의 평형상수를 구했다. 이 값으로부터 이들 착물생성에 대한 ${\Delta}H$, ${\Delta}G$및 ${\Delta}S$ 이 열역학적 파라미터를 산출하였다. 이 결과 착물의 상대적 안정도가 다음 순서로 증가함을 알수가 있었다. Pyridine < ${\beta}$-Picoline < 3,5-Lutidine. 이러한 결과는 dipole moment, steric hindrance effect 및 positive inductive effect에 의한 electron density의 증가 때문인 것으로 설명할 수 있었다. 그리고 polymethylbenzene-iodine CT-complex와도 비교 검토하였다.

• Nuclear Engineering and Technology
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• 제56권6호
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• pp.2079-2091
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• 2024

In this paper, a model is developed for calculating pH in the presence of organic impurities due to dissolution of paint and/or continuous injection of organic impurities in the sump. The model is implemented in the AnCheBi code for the analysis of chemical behaviors of the iodine in the containment when the pH changes during a severe accident. Validation of the model is performed with P10T2 and P11T1 experiments carried out by AECL in Canada under the BIP project. Importance analyses of the pH calculation model in the AnCheBi code are then performed with the aforementioned experimental data via Latin hypercube sampling on the reaction coefficients, sensitivity analyses of AnCheBi, and calculation of the correlation coefficients between the reaction coefficients and figure of merits (the pH and the concentrations of the various iodine species). From the importance analyses, we provide the sensitivity of the pH calculation model to the change of pH and the concentrations of the various iodine species and the reaction coefficients related with the dominant phenomena underlying the change of pH and the concentrations of the species.

• 한국수소및신에너지학회논문집
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• 제21권4호
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• pp.278-285
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• 2010

The Sulfur-Iodine (SI) thermochemical hydrogen production process of a closed cycle consists of three sections, which are so called the Bunsen reaction section, the $H_2SO_4$ decomposition section and the HI decomposition section. To identify the role of oxygen that can be supplied to the Bunsen reaction section via the $H_2SO_4$ decomposition section, Bunsen reactions with a $SO_2,\;SO_2-O_2$ mixture and $SO_2-N_2$ mixture as feed gases were carried out using a stirred reactor in the presence of $I_2/H_2O$ mixture. As the results, the amounts of $I_2$ unreacted under the feed of mixture gases were higher than those under the feed of $SO_2$ gas only, and the amount of HI produced was relatively decreased. The results of Bunsen reaction using $SO_2-O_2$ mixture were similar to those using $SO_2-N_2$ mixture. It may be concluded that an oxygen in $SO_2-O_2$ mixture has a role as a carrier gas like a nitrogen in $SO_2-N_2$ mixture. The effects of oxygen were decreased with increasing temperature and decreasing oxygen content in $SO_2-O_2$ mixture.

• 한국수소및신에너지학회논문집
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• 제19권6호
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• pp.490-497
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• 2008

For continuous operation of the sulfur-iodine(SI) thermochemical cycle, which is expected practical method for massive hydrogen production, suggesting operation conditions at steady state is very important. Especially, in the Bunsen reaction section, the Bunsen reaction as well as side reactions is occurring simultaneously. Therefore, we studied on the relation between the variation of compositions in product solution and side reactions. The experiments for Bunsen reaction were carried out in the temperature range, from 268 to 353 K, and in the $I_2/H_2O$ molar ratio of $0.094{\sim}0.297$ under a continuous flow of $SO_2$ gas. As the result, sulfur formed predominantly with increasing temperature and decreasing $I_2/H_2O$ molar ratios. The molar ratios of $H_2O/H_2SO_4$ and $HI/H_2SO_4$ in global system were decreased as the more side reaction occurred. A side reactions did not appear at $I_2/H_2O$ molar ratios, saturated with $I_2$, irrespective of the temperature change. We concluded that it caused by the increasing stability of an $I_{2x}H^+$ complex and a steric hindrance with increasing $I_2/HI$ molar ratios.

• 대한화학회지
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• 제37권10호
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• pp.855-860
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• 1993

SDS(sodium dodecyl sulfate) 존재하에서 NP-40EO[nonylphenol-(ethylene oxide)40]와 요오드와의 상호작용에 따른 $Ca^{2+}$의 영향을 UV-visible spectrophotometer를 이용하여 수용액 중에서 조사하였다. SDS 부재시보다 상호작용 피크의 흡광도는 줄어들었으며, CMC 이상에서 $Ca^{2+}$ 첨가에 따른 상호작용 피크의 강도는 크게 증가하였다. 상호작용 피크의 감소는 SDS 삽입에 따른 혼합미셀 단위 표면적당 요오드와 상호작용할 수 있는 EO 수의 감소에 기인하며, 상호작용 피크 강도의 증가는 $Ca^{2+}$ 존재하에서 미셀 구조가 더욱 조밀해진데 따른 전자주게-받게 겹침 증가로 불 수 있다. 이러한 현상들은 수용액 중에서 상대적으로 자유로운 배향을 갖는 선형 EO 사슬이 유사 크라운 에테르 구조를 형성하여 $Ca^{2+}$ 이온과 착물을 형성할 수 있는 가능성을 보여준다.