• 대한화학회지
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• 제26권2호
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• pp.88-94
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• 1982

요소공장의 굴뚝에서 방출되는 가스상 암모니아와 입자상 암모늄을 측정하여 대기중에서 암모니아가 암모늄으로 전환되는 속도를 추정하였다. 암모니아가 암모늄으로 전환되는 것은 대기중에서의 수송시간에 따라 2단계로 나누어진다. 수송 초기 15분동안의 전환속도는 3.2%ㅡmin$^{-1}$이고 그 후는 0.26%min$^{-1}$이었다. 수송 초기단계에서 전환속도가 빠른 것은 굴뚝에서 방출된 유출가스의 온도강하에 의하여 생성된 물방울에 암모니아가 용해하고, 또 이 알칼리성 물방울에서 요소가 분해반응을 일으킴으로써 암모늄의 농도가 급격히 증가하였기 때문인 것으로 추정되었다. 암모니아 가스의 반감기는 수송 초기단계에서 약 16분이고, 그 후는 192분이었다. 측정기간에 있어서 입자상 암모늄염과 대기온도, 상대습도, 이산화황, 질소산화물 및 부유분진 농도와의 사이에는 상관관계가 관찰되지 않았다.

• 한국세라믹학회지
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• 제35권1호
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• pp.5-10
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• 1998

Mullitization in a multicomponent oxide system(alumina-kaolin-quartz-feldspar-talc) was studied as a function of sintering temperature from 1200 to 1500$^{\circ}C$ based upon a quantitative X-ray diffraction analysis. In the present study mullite grew as wiskers and its formation reaction showed characteristic there stages as follows In the first stage(1255-1295$^{\circ}C$) an appreciable mullitization(nucleation) occurred while corun-dum dissolution into glass (increasing glass content ) limited the rate of the reaction. At 1295-1335$^{\circ}C$ (second state) the reaction was significantly enhanced with a considerable glass consumption and with no appreciable change in corundum content. Finally (above 1335$^{\circ}C$) the reaction rate was attenuated re-markably with an apparent decrease in glass consumption rate. The impingement of mullite whiskers by oth-er whiskers and crystals was speculated to cause mullite growth in thickness direction with a slow growth rate resulting in the diminished reaction rate in the final stage.

• 한국세라믹학회지
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• 제50권4호
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• pp.301-307
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• 2013

SiC hollow fiber was fabricated by curing, dissolution and sintering of Al-PCS fiber, which was melt spun the polyaluminocarbosilane. Al-PCS fiber was thermally oxidized and dissolved in toluene to remove the unoxidized area, the core of the cured fiber. The wall thickness ($t_{wall}$) of Al-PCS fiber was monotonically increased with an increasing oxidation curing time. The Al-PCS hollow fiber was heat-treated at the temperature between 1200 and $2000^{\circ}C$ to make a SiC hollow fibers having porous structure on the fiber wall. The pore size of the fiber wall was increased with the sintering temperature due to the decomposition of the amorphous $SiC_xO_y$ matrix and the growth of ${\beta}$-SiC in the matrix. At $1400^{\circ}C$, a nano porous wall with a high specific surface area was obtained. However, nano pores grew with the grain growth after the thermal decomposition of the amorphous matrix. This type of SiC hollow fibers are expected to be used as a substrate for a gas separation membrane.

• 한국물환경학회지
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• 제23권2호
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• pp.193-200
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• 2007

The AOPs research defined by creating a sufficient amount of OH radicals from the dissolution of organic materials through photoxidation and research for a complete elimination of residual organic materials by membrane are actively ongoing. This research focuses on the hybrid processing of AOPs and M/F membrane to dissolve and eliminate organic chemicals in drinking water which are suspected of carcinogens. For this purpose, underground water was used as a source of drinking water for the hybrid processing of AOPs oxidation and M/F membrane, and a pilot plant test device was installed indoor. Carcinogenic chemicals of VOCs and pesticide were artificially mixed with the drinking water, which was then diluted close to natural water in order to examine treatment efficiency and draw optimal operation conditions. The samples used for this experiment include four chemicals phenol, chloroform, in VOCs and parathion, carbaryl in pesticide. As a result of the experiments conducted with simple, and compound solutions, the conditions to sufficiently dissolve and eliminate carcinogenic chemicals from the hybrid processing of where carcinogens were artificially added are : (hydrogen peroxide) prescribed solution 100 mg/L under pH 5.5~6.0, and the temperature $12{\sim}16^{\circ}C$, at the normal temperature and pressure. $d-O_3$ volume of 5.0 ppm and above and 30-40 minutes of reaction time are most appropriate and using MF/UF for membrane was ideal.

• 자원리싸이클링
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• 제17권1호
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• pp.66-72
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• 2008

폐알칼리망간전지로부터 침출과 공침반응을 이용하여 Mn-Zn ferrite 분말을 제조하기 위한 기초실험을 수행하였다. 100g/L 광액 농도 3.0M $H_2SO_4$, $60^{\circ}C$ 및 교반속도 200 rpm의 조건에서 과산화수소 30ml를 첨가하여 얻어진 아연과 망간의 침출율은 각각 97.9%, 93.9% 이상이었으며, 침출용액을 가지고 반응시간, 반응온도, $O_2$ 가스량을 조절하며 공침반응을 진행하였다. 공침반응 결과 pH 12, $80^{\circ}C$, $O_2$ 1.3L/min, 교반속도 400 rpm의 조건에서 Mn-Zn ferrite를 저온 합성할 수 있었다. 합성된 Mn-Zn ferrite분말은 $0.143{\mu}m$의 구형 ferrite로서 80 emu/g의 포화자화값을 가지고 있었다.

• 자원리싸이클링
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• 제17권1호
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• pp.38-42
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• 2008

암모니아 용액중에서 바나듐(V)의 침출 시 바나듐의 용해와 후공정에서 $NH_4VO_3$로 침전 회수를 위한 조건에 관한 기초연구를 수행하였다. 침출공점에서 바나듐의 용해도를 높이기 위해서는 높은 온도가 필요하며 $(NH_4)_2CO_3$ 20g/L와 $NH_4OH$ 2.5M의 혼합 용액에서 반응온도가 $90^{\circ}C$일 때 용액 중 바나듐 농도가 16.8g/L이다. 한편 용해된 바나듐을 침전물 형태로 회수하기 위해서는 $25^{\circ}C$에서 $NH_4Cl$을 20g/L를 첨가하고 72시간 정치했을 때 용액에 잔류 바나듐의 농도를 0.0268g/L까지 낮출 수 있었으며 이 경우 바나듐의 회수율은 99.8%이었다.

• 한국정보전자통신기술학회논문지
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• 제12권1호
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• pp.72-77
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• 2019

정보전달 매체 중 시각을 통하여 우리에게 정보를 제공해 주는 디스플레이는 직관적으로 정보를 전달해 줌으로써 매우 중요한 정보전달 수단이라고 할 수 있으며 액정표시장치는 디스플레이 중에서 가장 많이 보급되어 있는 정보전달기기라고 할 수 있다. 본 논문에서는 액정디스플레이 제작을 위하여 필수적인 러빙 기반 액정 배향 공정을 대체할 수 있는 공정으로서 solvent assisted micromolding을 연구하였으며 가장 일반적인 액정 배향막인 polyimide에 나노구조를 형성함으로써 균일하게 액정 배향을 달성하고자 하였다. Polyimide 나노구조 형성 시 공정 온도에 따라 용매에 의한 고분자 용해효과와 몰드의 나노구조 안으로 polyimide 분자의 모세관 효과 사이의 상보적 상관관계가 존재하였으며 최적온도 도출을 통해 높은 단차를 갖는 나노구조를 형성할 수 있었다. 이러한 나노구조는 액정 분자를 균일하게 배향할 수 있었으며 일정한 선경사각을 형성할 수 있음을 증명하였다.

• Corrosion Science and Technology
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• 제21권5호
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• pp.381-389
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• 2022

Cyclic Voltammetry and weight loss measurements were used to investigate corrosion prevention of tin in a 0.5M citric acid solution containing Anthocyanins extracted from grapes at various concentrations and temperatures. Results showed that the investigated chemicals, Anthocyanins extracted from grapes, performed well as tin corrosion inhibitors in 0.5M citric acid. Increasing the concentration of Anthocyanins increased their corrosion inhibition efficiencies. When the temperature dropped, their inhibition efficiencies, increased indicating that higher temperature tin dissolution predominated the adsorption of Anthocyanins at the surface of tin metal. When inhibitor concentrations were increased, their inhibition efficiencies were also increased. These results revealed that corrosion of tin metal was inhibited by a mixed type of adsorption on the metal surface. The adsorption isotherm of Langmuir governed the adsorption of Anthocyanins. Thermodynamic parameters such as the enthalpy of adsorption, the entropy of adsorption, and Gibbs free energy and kinetic parameters such as activation energy, enthalpy of activation, and entropy of activation were computed and discussed in this study.

• 청정기술
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• 제28권2호
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• pp.147-154
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• 2022

Titanate nanotubes (TNTs) were synthesized via alkaline hydrothermal treatment using commercial TiO₂ nanoparticles (P25). The TNTs were prepared at various TiO₂/NaOH ratios, hydrothermal temperatures, and hydrothermal times. The synthesized catalysts were characterized by X-ray diffraction, field-emission scanning electron microscopy, N₂ adsorption-desorption isotherms, field-emission transmission electron microscopy, and ultraviolet-visible spectroscopy. TNTs were generated upon a decrease in the TiO₂/NaOH ratio due to the dissolution of TiO₂ in the alkaline solution and the generation of new Ti-O-Ti bonds to form titanate nanoplates and nanotubes. The hydrothermal treatment temperature and time were important factors for promoting the nucleation and growth of TNTs. The TNT catalyst with the largest surface area (389.32 m² g^-1) was obtained with a TiO₂/NaOH ratio of 0.25, a hydrothermal treatment temperature of 130 ℃, and a hydrothermal treatment time of 36 h. Additionally, we investigated the photocatalytic activity of methyl violet 2B (MV) over the TNT catalysts under UV irradiation and found that the degradation efficiencies of the TNTs were higher than that of P25. Among the TNT catalysts, the TNT catalyst that was hydrothermally synthesized for 36 h (TNT 36 h) exhibited a 96.9% degradation efficiency and a degradation rate constant that was 4.8 times higher than P25 due to its large surface area, which allowed for more contact between the MV molecules and TNT surfaces and facilitated rapid electron transfer. Finally, these results were correlated with the specific surface area.

• 대한환경공학회지
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• 제28권1호
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• pp.54-60
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• 2006

주문진사 및 석영사를 담체로 사용하여 코팅온도, 코팅시간, 및 초기 망간용액 주입농도를 변화시키면서 망간(IV)을 코팅시킨 모래흡착제($MnO_2$-Coated Sand, MCS)를 제조하였으며 As(III)의 산화효율을 비교하였다. MCS 제조의 최적조건은 코팅효율 및 As(III) 산화능으로 부터 선정하였다. 망간 코팅효율은 코팅시간에는 크게 영향을 받지 않았지만 코팅온도가 증가함에 따라 증가하였다. 반면 As(III)의 산화능은 코팅온도가 증가됨에 따라 크게 감소하여 나타났다. 이러한 결과들을 고려하여 MCS의 최적 코팅 조건을 $150^{\circ}C$ 온도조건과 1시간의 가열시간으로 선정할 수 있었다. Mn(II) 주입농도가 늘어남에 따라 망간 코팅효율은 뚜렷이 증가하였지만 As(III)의 산화능은 0.8 Mn(II) mol/kg sand 조건에서 최대값을 보여주었다. MCS로 부터의 망간의 용출은 pH가 감소함에 따라 크게 증가하여 나타났다. 최적 조건에서 제조한 MCS를 사용하여 As(III)의 산화반응 특성을 회분식 실험을 통하여 조사한 결과, MCS의 As(III) 산화특성은 MCS의 농도에 대하여 비례적인 반응속도를 보여주었으며 pH가 감소할수록 As(III)의 산화속도가 증가하였다.