• Applied Chemistry for Engineering
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• v.24 no.4
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• pp.337-343
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• 2013

Membrane reactors have been showing a promising future and attracted increasing attention in the scientific community as they possess advantages in terms of enhanced catalytic activity and selectivity, combination of processes (reaction and separation), simplicity in process design, and safety in operation. In particular, solid electrolyte membrane reactor principles are realized in fuel cells, electrolyzers and reactors for hydrogenation of carbon dioxide and other economically viable reactions. In this review, as a young generation of ion conducting materials, high temperature proton conductors are discussed in terms of the current status of material development and their various applications.

• Journal of the Korean Chemical Society
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• v.63 no.3
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• pp.216-219
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• 2019

• Proceedings of the Mineralogical Society of Korea Conference
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• 2001.06a
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• pp.7-7
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• 2001

다량의 점토 퇴적물로 구성된 연약지반은 대단히 큰 압축성과 낮은 강도, 높은 함수량등의 물리·역학적 특성을 갖는다. 이러한 기초지반으로서의 불리한 특성 때문에 이를 대상으로 하는 각종 토목건설공사에서는 지반개량이나 안정처리가 반드시 선행되어야 할 과제이다. 이를 위해 종래에는 샌드드레인, 페이퍼드레인 등의 물리적인 공법에 의한 지반개량이 주류를 이루었으나, 최근에는 생석회나 시멘트계 고화재를 이용한 화학적 안정 처리공법이 크게 주목을 받고 있어 이에 대한 연구가 활발한 상황이다. 본 연구는 연약 지반 안정처리에 대한 방안을 모색하기 위하여 김해 지역에 분포하는 점토 퇴적물을 대상으로 각종 광물재료를 이용한 반응실험을 통하여 반응생성물 조사와 압축강도시험 등을 행하여 그 결과를 검토하였다. 우선 연약지반의 고화에 이용 가능한 생석회, 석고, 플라이에쉬, 고분자폴리머, 시멘트 등을 사용하여 점토와 혼합한 고화실험을 행하였으며, 이에 대한 물성 및 반응생성물을 검토하였다. 이러한 각 재료를 점토에 혼합한 후 PVC관에 모울딩하여 양생시켜 실험하였다. 그 결과, 석고 및 소석회에 비하여 생석회의 경우가 비교적 큰 압축강도를 나타내고, 균열발생 빈도도 낮았다. 생석회의 경우에 Gehlenite, Hillebrandite 등의 생성물질이 검출되었다. 그러나 포틀란트 시멘트와 혼합한 경우가 강도가 가장 크게 나타났다. 반면에 고분자폴리머만 사용한 경우는 강도가 매우 낮았다. 따라서 시멘트를 일정 비율로 배합한 다른 재료를 첨가한 실험을 행하여 그 물성을 검토하였다 물질의 화학적인 특성을 고려하여 포졸란반응이 잘 일어날 수 있을 것으로 생각되는 여러 재료를 선정하여 많은 조합에 대한 실험을 행하였다. 생석회, 석고, 고령토, 규조토, 제올라이트 등의 여러 재료를 여러 조합으로 첨가하여 실험한 결과, 시멘트와 석고를 혼합한 것이 비교적으로 높은 압축강도를 나타내었다. 그리고 이러한 연구 결과를 바탕으로 연약점도의 고화에 최적인 조합과 배합비를 위한 실험을 재차 실시하였으며, 실험 후의 물성과 함께 반응생성물에 대한 검토도 행하여 그 결과를 발표하고자 한다.

• Applied Chemistry for Engineering
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• v.19 no.5
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• pp.526-532
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• 2008

The proposed $CO_2$ storage technology in the present study is a one-step sequestration process that stabilizes $CO_2$ in a reactor with Serpentine. The advantage of this technology is associated with its high stability of final product so that the entire system is recognized as permanent environment-friendly $CO_2$ removal method. Since the sequestration reaction mechanisms are generally understood that carbonation reaction proceeds with very slow rate, so that pretreatment method to increases reaction rate of $CO_2$ carbonation reaction should be developed. To increase the reactivity of Serpentine with $CO_2$, two different methods of pretreatment are carried out in the present investigation. One is heat-treatment, the other is chemical pretreatment. In this study, only chemical pretreatment is considered leaching method of magnesium from Serpentine using sulfuric acid at the various reaction temperatures, times, and acid concentrations. Experimental results illustrated that pretreatment by sulfuric acid increases surface area of serpentine from $11.1209m^2/g$ to $98.7903m^2/g$ and extracts magnesium compounds. Single variable experiment demonstrated the enhancements of magnesium extraction with increased reaction temperature and time. Amount of magnesium extraction is obtained by using the data of ICP-AES as maximum extraction condition of magnesium is 2 M acid solution, $75^{\circ}C$ and 1hr. After performing chemical pretreatment, carbonation yield increased from 23.24% to 46.30% of weight.

• Journal of the Korean Chemical Society
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• v.35 no.2
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• pp.165-171
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• 1991

The electrochemical reduction of carbon-6-dibromo groups on 6,6-dibromo penicillanic acid 1,1-oxide(DBPA) was investigated by direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The irreversible two electrons transfer on the reductive debromination of each bromo group proceeded by EC,EC mechanism at the two electrode reduction steps(-0.48, -1.62 volts). The 6-bromo-PA and 6,6-dihydro-PA was synthesized by controlled potential electrolysis. Upon the basis of results on the products analysis and interpretation of polarograms obtained at various pH, electrochemical reaction mechanism was suggested.

• Korean Chemical Engineering Research
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• v.46 no.5
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• pp.1013-1016
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• 2008

Nitrogen in the form of nitrate was electrochemically reduced with different cathode materials including Fe, Ni, Cu, and Zn. Zn cathode shows the greatest electrocatalytic activity on the transformation of nitrate ions into ammonia and the $NO_3^-$ removal efficiency has highest value at pH 8.5. Nitrogen in the form of nitrate was initially reduced into nitrite and sequentially, converted into nitrogen inside $NH_3$. Nitrogen in the form of ammonia was completely removed by the reaction with HOCl.

• Journal of the Korean Chemical Society
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• v.38 no.1
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• pp.61-68
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• 1994

The intramolecular formal iron-catalyzed [4+2] cycloaddition reaction of acetylenic dienes to produce bicyclic products has been investigated. These reactions proceeded, competing via intramolecular carbocyclization and bimolecular cycloaddition. However, the iron-catalyzed bicyclic carbocyclization of 4,4-dimethyl-3-(tert-butyldimethylsiloxy)-1-phenyl-6,8-decadien-1-yne(11) yielded exclusively bicyclic diene product(yield 78.1%). From this result, we found that the substrate containing a dimethyl substitutent at the 4,4-position helped to promote the intramolecular reaction, which is stable to the iron catalyzed conditions.

• 한국신재생에너지학회:학술대회논문집
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• 2009.11a
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• pp.199-202
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• 2009

본 연구에서는 내부 개질반응에서 사용되는 고함량의 니켈촉매(Ni/Al2O3계열 촉매)제조를 위해, 요소(urea)를 이용한 균일용액 침전법을 이용하여 니켈이 고분산된 52wt% Ni/$Al_2O_3$ 촉매를 제조하였다. 제조 촉매는 BET 표면적, 니켈분산도, 니켈표면적 등 물리.화학적 물성 모두 우수하였으며, 환원 패턴은 상용촉매와 비슷하게 나타났다. 실제 반응온도인 $650^{\circ}C$에서 소성하여 화학흡착을 비교한 결과,상용촉매는 니켈분산도 및 니켈표면적이 감소한 반면 균일용액 침전법으로 제조한 촉매는 거의 변화가 없었다. 개질 성능 또한 상용촉매보다 우수하였는데, 이것은 균일용액 침전법으로 제조한 촉매는 활성점(니켈)이 지지체에 나노사이즈로 고르게 잘 분산되었기 때문이라고 판단하였다. 또한 합성온도 조절을 통해, $650^{\circ}C$ 소성 후에 물성변화를 살펴보았고 합성온도 $85^{\circ}C$에서 고분산 니켈 촉매 제조가 가능하였다.

• Journal of the Korean Chemical Society
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• v.35 no.6
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• pp.707-712
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• 1991

N'-phenyl-N-(2-chloroethyl)-N-aminourea has been prepared from N'-phenyl-N-(2-chloroethyl)-N-nitrosourea by means of the electrochemical reduction with the mercury pool electrolytic cell. In order to find out the optimum condition of the reaction, the voltammetric behaviors for N'-aryl-N-(2-chloroethyl)-N-nitrosourea derivatives have been investigated by the cyclic voltammetry and polarography. The peak potentials was shifted to the negative direction as the pH value of the solution decrease. The substituent effects of phenyl ring on the peak potential were not observed in this case. (5:3) EtOH/4 N-HCl mixed solution was employed for the electrolysis. The applied potential was -0.7 V vs. Ag/AgCl/4 N-HCl electrode. The number of electrons participated to the reduction process was 4, respectively. The product was identified by FT-IR, NMR, mass and/or elemental analysis data.

• Journal of the Korean Chemical Society
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• v.54 no.4
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• pp.419-428
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• 2010

Here we describe a fast and rapid technique for preparation of amino acid hydrazide as well as peptide hydrazide derivatives using diisopropylcarbodiimide (DIC)/1-hydroxybenzotriazoles (HOXt) (X = A or B) under microwave irradiation employing a multimode reactor (Synthos 3000 Aton Paar, GmbH, 1400 W maximum magnetron). A comparison between conventional and microwave irradiation was described. The microwave methodology is rapid, convenient, proceeds under mild conditions. Diisopropylcarbodiimide (DIC)/7-aza-1-hydroxybenzotriazole (HOAt) always gave much better yield (95 - 98%) and purity than diisopropylcarbodiimide (DIC)/1-hydroxybenzotriazole (HOBt).