• 한국결정성장학회지
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• 제13권1호
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• pp.24-30
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• 2003

The preparation of $PbTiO_3$ powder was carried out using the oxide starting material by hydrothermal method. The powder of a crystalline phase with perovskite structure was synthesized. The optimum conditions for the preparation of powder were as follows; hydrothermal solvent; 8M-KOH or 8M-NaOH, reaction temperature; 250~$270^{\circ}C$, run time; 10 h. The ,shape of synthesized powders were well developed crystalline faces with specific surface area of about 2.3 $\textrm m^2$/g in KOH solution and about 5.0 $\textrm m^2$/g in NaOH solution. The cell parameters of powder were a = 3.90$\AA$, c = 4.14 $\AA$ and cell volume was 57.30 $\AA^3$. The cell ratio (c/a) of powder was the same as the theoretical ratio with c/a = 1.06 and the phase transition temperature(Tc) of the powders was about $470^{\circ}C$.

• Carbon letters
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• 제8권1호
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• pp.30-36
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• 2007

Oxidized PAN (OXI-PAN) fibers were used for the precursors of activated carbon fiber in study. How drying temperature affected the properties of carbon fibers on activating process of carbon fibers was investigated. The specific surface areas of activated carbon fibers have been determined on a series of chemically activated carbons with KOH and NaOH. The experimental data showed variations in specific surface area, iodine and silver adsorptions by the activated carbon fibers. The amount of iodine adsorption increases with increasing specific surface areas in both activation methods. This was because the ionic radius of iodine was smaller than the interior micropore size of activated carbon fibers. Silver adsorbed well in NaOH activated carbon fibers rather than KOH activated carbon fibers in this study.

• 약학회지
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• 제46권6호
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• pp.369-374
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• 2002

Dilithiation of 4-(pivaloylamino)pyridine (5) followed by reaction with tetraisopropylthiuram disulfide(TITD) gave rise to 3-(diisopropyldithiocarbamato)-4-(pivaloylamino)pyridine (6). 3-Mercapto-4H-pyrrolopyridine(2) was synthesized from compound 6 by two methods. The first method was that compound 6 was treated with 5M-HCl to form 2-t-butylthiazolo[5,4-c]pyridine (7) and hydrolysed in refluxing 10％ NaOH and solid NaOH to prepare bis(4-amino-3-pyridyl)disulfide (8). And compound 8 was reacted with 2,5-dimethoxytetrahydrofuran and NaBH$_4$ to afford compound 2. The second method was that compound 6 was hydrolysed with 10％ NaOH and followed to react with 2,5-dimethoxytetrahydrofuran to form compound 11. And then compound 11 was treated with 20％ ethanolic KOH solution to synthesize compound 2.

• 열처리공학회지
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• 제37권1호
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• pp.16-22
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• 2024

The conventional degreasing process involves removing oil and contaminants at temperatures above 80℃, resulting in excessive energy consumption, increased process costs, and environmental issues. In this study, we aimed to find the optimal degreasing conditions for the pre-treatment process of electro-galvanizing cold-rolled steel sheets, conducted efficiently at room temperature without the need for a separate heating device. To achieve this, we developed a room temperature degreasing solution and a brush-type degreasing tool, aiming to reduce energy consumption and normalize the decrease in degreasing efficiency caused by temperature reduction. Alkaline degreasing solution were prepared using KOH, SiO₂, NaOH, Na₂CO₃, and Sodium Lauryl Sulfate, with KOH and NaOH as the main components. To enhance the degreasing performance at room temperature, we manufactured additives including sodium oleate, sodium stearate, sodium palmitate, sodium lauryl sulfate, ammonium lauryl sulfate, silicone emulsion, and EDTA-Na. Room temperature additives were added to the alkaline degreasing solution in quantities ranging from 0.1 to 20 wt.%, and the uniformity of degreasing and the adhesion of the galvanized layer were evaluated through Dyne Test, T-bending Test, OM, SEM, and EDS analyses. The results indicated that the optimal degreasing solution composition consisted of NaOH (30 g/L), Na₂CO₃ (30 g/L), SLS (6 g/L), and room temperature additives (≤1 wt%).

• 한국재료학회지
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• 제23권11호
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• pp.643-648
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• 2013

Activated carbon (AC) was synthesized from rice husks using the chemical activation method with KOH, NaOH, a combination of (NaOH + $Na_2CO_3$), and a combination of (KOH + $K_2CO_3$) as the chemical activating reagents. The activated carbon with the highest surface area (around $2000m^2/g$) and high porosity, which allows the absorption of a large number of ions, was applied as electrode material in electric double layer capacitors (EDLCs). The AC for EDLC electrodes is required to have a high surface area and an optimal pore size distribution; these are important to attain high specific capacitance of the EDLC electrodes. The electrodes were fabricated by compounding the rice husk activated carbons with super-P and mixed with polyvinylidene difluoride (PVDF) at a weight ratio of 83:10:7. AC electrodes and nickel foams were assembled with potassium hydroxide (KOH) solution as the electrolyte. Electrochemical measurements were carried out with a three electrode cell using 6 M KOH as electrolyte and Hg/HgO as the reference electrode. The specific capacitance strongly depends on the pore structure; the highest specific capacitance was 179 F/g, obtained for the AC with the highest specific surface area. Additionally, different activation times, levels of heating, and chemical reagents were used to compare and determine the optimal parameters for obtaining high surface area of the activated carbon.

• KSBB Journal
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• 제11권2호
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• pp.159-164
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• 1996

폐식용유와 알코올의 에스테르화 반응에 의한 바이오 디젤유 제조 실험을 하였다. 실험 조건은 폐식용유 대 얄코올의 흔합 몰비0:3, 1:5, 1:7), 촉매 의 양(0.5, 1.0, 1.5wt.% , 촉매종류(sodium meth-oxide, NaOH, KOH), 반응온도(30, 45, $50^{\circ}C$), 알코올 종류(메탄올, 에탄올, 부탄올) 등이다. 폐식용유 대 알코올 혼합 몰비가 증가하면 할수록 전환율 은 증가하였고, sodium methoxide, NaOH, KOH 촉매 종류의 영향은 크지 않았다. 반응 온도(30, 45, $50^{\circ}C$), 의 영향에서 반응 온도가 증가할수록 전환율은 증가하였고, 메탄융,에탄융,부탄올 중 메탄올 사용시 전환율이 가장 높았다. 에스테르반응 후 경 유와 물성을 비교하여 보면 점도가 다소 높게 나타 났으나,전체적무로 폐식용유의 물성이 개선되어 연료로서의 사용성이 개선되었다.

• 한국결정성장학회지
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• 제12권3호
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• pp.126-132
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• 2002

$ZrOCl_2{\cdot}8H_2O$ 수용액과 KOH 수용액의 반응으로부터 얻은 침전물을 $100^{\circ}C$에서 24 시간 동안 숙성시켜 정방정상 지르코니아를 제조한 후 수열합성 조건을 변화시킴으로써 비등방성 형상의 나노 결정형 지르코니아 분말을 합성하였다. 수열합성 시 반응온도와 반응시간이 증가할수록 정방정상인 구형 입자는 감소하고 상대적으로 단사정상 spindle-like 입자와 막대상 입자가 증가하였다. NaOH 용액의 농도가 증가함에 따라 입성장과 함께 정방정상에서 단사정상으로의 상전이가 촉진되었으며, 저온에서 반응시간이 짧은 경우 합성한 분말들은 반응초기에 응집된 입자들이 NaOH 용액에 부분적으로 용해되면서 응집입자 및 결정입자 크기가 감소되어 비표면적이 증가하였다가 반응시간이 길어지고 반응온도가 높아짐에 따라 입성장에 의하여 점차 비표면적이 감소하였다.

• 자원리싸이클링
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• 제14권1호
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• pp.47-54
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• 2005

본 연구에서는 농산물 폐기물인 국산 포도씨를 원료로 사용하여 roasting, cabonization, chemical activation 과정을 각각 거쳐 활성탄을 제조하였다. 화학적 활성화는 NaOH, KOH, ZnCl$_2$를 활성화제로 사용하였다. 100-300wt%의 중량비율로 활성화하여 제조된 활성탄의 N$_2$-BET 비표면적은 44.09~121.33 m$^2$/g으로 측정되었다. 포도씨 활성탄에 메틸렌 블루를 흡착 시킨 후 UV spectrometer를 사용하여 투광도를 측정하였으며, 투광도 측정 시 메틸렌 블루의 최대 흡광파장은 660 nm로 설정하였다. 그 결과 메틸렌블루의 흡착은 NaOH 활성화제를 사용하여 제조한 활성탄에서 가장 잘 이루어졌으며, 평형 흡착 시간은 60분인 것으로 나타났다.

• 유기물자원화
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• 제16권4호
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• pp.50-56
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• 2008

본 연구는 볏짚, 보리짚, 밀짚 및 유채대를 이용한 액화공정을 적용하여 중유를 생산할 때 그 생산량을 비교하였다. 촉매제로 $K_2CO_3$, NaOH 및 KOH와 같은 촉매제를 사용하여 반응온도 $320^{\circ}C$에서 10분간 반응시켰다. 액화공정 시스템은 외부전기화로, 교반기 및 5,000ml 반응기로 구성되어 있다, 반응기에 식물체 잔사 160g, 증류수 2,000ml 및 촉매제를 혼합하였으며, 촉매제량은 식물체 잔사량의 10%(wt/wt)를 투입하였다. KOH 촉매제를 사용하며, 보릿짚을 이용할 경우 바이오매스 투입량과 비교하여 최고 중유 생산량은 29%였다. 바이오매스 발열량과 비교하여 식물체 잔사로부터 전환된 중유의 발열량은 55~66% 범위이었다. 밀짚으로부터 전환된 중유의 발열량은 약 6190 kcal/kg으로 가장 높게 관측되었다.

• Bulletin of the Korean Chemical Society
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• 제33권12호
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• pp.4227-4230
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• 2012