• Membrane and Water Treatment
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• 제8권4호
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• pp.311-321
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• 2017

Hydrophilic and high modulus PPTA molecules were incorporated into PVDF matrix via the in situ polymerization of PPD and TPC in PVDF solution. PPTA/PVDF/NWF blend membrane was prepared through the immersion precipitation phase inversion method and nonwoven coating technique. The membrane integrated technology including PPTA/PVDF/NWF blend membrane and reverse osmosis (RO) membrane was employed to treat the polyester/viscose spunlace nonwoven process wastewater. During the consecutive running of six months, the effects of membrane integrated technology on the COD, ammonia nitrogen, suspended substance and pH value of water were studied. The results showed that the removal rate of COD, ammonia nitrogen and suspended substance filtered by PPTA/PVDF blend membrane was kept above 90%. The pH value of the permeate water was about 7.1 and the relative water flux of blend membrane remained above 90%. After the deep treatment of RO membrane, the permeate water quality can meet the water circulation requirement of spunlace process.

• 대한설비공학회:학술대회논문집
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• 대한설비공학회 2006년도 하계학술발표대회 논문집
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• pp.52-57
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• 2006

This study investigates the distribution stability of binary nanofluids where binary mixtures such as $NH_3/H_2O$ and $H_2O/LiBr$ solution are used as a base fluid. When a little amount of certain nanosized particles is added into a basefluid, the thermal conductivity of that mixture increases greatly. Such mixtures are named 'nanofluids' where nano-particles should be distributed stably and uniformly so the distribution stability of nanoparticles in nanofluids is one of the most important factors for nanofluid application. Therefore, binary nanofluids in which binary mixtures are applied as the basefluids are considered as working fluids. The kind and the concentration of nanoparticles, and the concentration of ammonia are considered as the key parameters. The objectives of this paper are to visualize the dispersed status of particles in binary nanofluids and to find the effect of key parameters on the distribution stability in the ammonia absorption system.

• 대한환경공학회지
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• 제30권12호
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• pp.1287-1293
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• 2008

기존의 연구에서 널리 사용된 흡수제 2-amino-2-methyl-1-propanol (AMP)의 성능 개선을 위해 carbon dioxide (CO$_2$) 및 nitrogen dioxide (NO$_2$)의 흡수율이 우수한 ammonia (NH$_3$)를 첨가하여 평면교반조에서 CO$_2$, NO$_2$ 및 CO$_2$/NO$_2$의 흡수속도실험을 수행함으로써 반응속도상수를 AMP 단일흡수제와 비교하였다. 30 wt.% AMP에 1, 3, 5 wt.%의 NH$_3$ 첨가에 따라 흡수속도는 대표적으로 303 K, 1 kPa NO$_2$ 분압에서 12.6$\sim$32.6% 증가되므로 NH$_3$의 첨가로 반응속도를 향상시켜 공정 효율의 증가를 기대할 수 있을 것으로 예상된다. 또한 30 wt.% AMP에 3 wt.% NH$_3$ 첨가 수용액의 NO$_2$ 분압 1 kPa과 CO$_2$ 분압 15 kPa에서 CO$_2$/NO$_2$ 동시 흡수속도는 5.50$\sim$6.40$\times$10$^{-6}$ kmol m$^{-2}$ s$^{-1}$로 NH$_3$의 CO$_2$ 및 NO$_2$에 대한 높은 부하능 및 추가 반응에 기인하여 AMP 단일수용액에 비해 48.2$\sim$41.6% 증가하였다. 또한, 화력발전소에서 배출되는 연소배가스 조성과 같이 CO$_2$ 15 kPa 및 NO$_2$의 비교적 낮은 분압(1 kPa) 조건에서 NO$_2$는 AMP에 NH$_3$ 첨가에 따라 약 2배의 빠른 반응으로 CO$_2$의 흡수에 큰 영향 없이 NO$_2$를 동시에 흡수할 수 있을 것으로 기대된다.

• 한국자동차공학회논문집
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• 제20권4호
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• pp.125-132
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• 2012

Urea-SCR system, which converts nitrogen oxides to nitrogen and water in the presence of a reducing agent, usually AdBlue urea solution, is known as one of the powerful NOx reduction systems for mobile as well as stationary applications. For its consistent and reliable operation in mobile applications, such various problems as transient injection, ammonia slip, and freezing in cold weather have to be resolved. In this work, therefore, numerical study on three-dimensional unsteady heating problems were analyzed to understand the melting and heat transfer characteristics such as urea liquid volume fraction, temperature profiles and generated natural convection behavior in urea solution by using the commercial software Fluent 6.3. After validating by comparing numerical and experimental data with pure gallium melting phenomena, numerical experiment for urea melting is conducted with three different coolant heating models named CH1, 2, and 3, respectively. Finally, it can be found that the CH3 model, in which more coolant is concentrated on the lower part of the urea tank, has relatively better melting capability than others in terms of urea quantity of $1{\ell}$ for start-up schedule.

• 설비공학논문집
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• 제21권8호
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• pp.433-438
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• 2009

Experimental results for performance characteristics of small $NH_3$ absorption chiller/ heater are presented. The apparatus consists of 7RT water-cooled absorption system, solution pump, boiler, cooling tower and peripheral devices. The effect of experimental parameters, such as refrigerant mass flow rate, solution mass flow rate and cooling water temperature have been investigated in view of the system performance. The capacity of each heat exchanger increased as refrigerant mass flow rate increased in cooling mode. Also, a cooling capacity increased as a strong solution mass flow rate increased. The cooling and heating COP show 0.5, 1.5 regardless of refrigerant mass flow rate, respectively. The results focus on the evaluation for performance characteristics of system with respect to variation of refrigerant mass flow rate under standard design conditions.

• 접착 및 계면
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• 제3권3호
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• pp.7-14
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• 2002

Poly(ethylene-co-methylacrylate)(PEMA)를 KOH, 암모니아 수용액으로 가수분해, ammonolysis 시켜서 측기에 -COOK, $-CONH_2$, -COOH를 갖는 수분산 형태의 변성 폴리에틸렌(m-PE)을 제조하였다. Infrared spectroscopy, 원소 분석 및 atomic absorption 분석 등을 통하여 m-PE 측기의 종류 및 조성비를 조사하였으며 수분산액의 고형분 함량에 따른 점도 및 표면장력을 측정하였다. 제조된 수분산액은 측기의 조성에 따라 안정도, 투명도 등이 변화하였다. 측기 중에서 -COOK가 수분산에 가장 큰 영향을 주었으며 -COOK 조성비가 20 mol% 이상이 되어야 안정한 분산을 얻을 수 있었고 또한 -COOK 조성비가 높을수록 수분산액은 투명하였다. 동일 -COOK 조성비에서는 아마이드의 농도가 높을수록 탁도가 증가하여 친수성이 떨어짐을 알 수 있었다. 분산액의 고형분 함량에 따른 점도를 측정하면 -COOK 조성비가 클 경우 낮은 고형분 함량에서 급격한 점도 증가가 일어나 고분자 사슬사이의 얽힘이 쉽게 일어남을 알 수 있으며 표면장력은 -COOK 조성비가 클 경우 작은 값을 나타내었다.

• 한국분말재료학회지
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• 제20권3호
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• pp.180-185
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• 2013

The iron oxides nanoparticles and iron oxide with other compounds are of importance in fields including biomedicine, clinical and bio-sensing applications, corrosion resistance, and magnetic properties of materials, catalyst, and geochemical processes etc. In this work we describe the preparation and investigation of the properties of coated magnetic nanoparticles consisting of the iron oxide core and organic modification of the residue. These fine iron oxide nanoparticles were prepared in air environment by the co-precipitation method using of $Fe^{2+}$: $Fe^{3+}$ where chemical precipitation was achieved by adding ammonia aqueous solution with vigorous stirring. During the synthesis of nanoparticles with a narrow size distribution, the techniques of separation and powdering of nanoparticles into rather monodisperse fractions are observed. This is done using controlled precipitation of particles from surfactant stabilized solutions in the form organic components. It is desirable to maintain the particle size within pH range, temperature, solution ratio wherein the particle growth is held at a minimum. The iron oxide nanoparticles can be well dispersed in an aqueous solution were prepared by the mentioned co-precipitation method. Besides the iron oxide nanowires were prepared by using similar method. These iron oxide nanoparticles and nanowires have controlled average size and the obtained products were investigated by X-ray diffraction, FESEM and other methods.

• 한국재료학회지
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• 제18권2호
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• pp.69-72
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• 2008

A sensor element array for combinatorial solution deposition research was fabricated using LTCC (Low-temperature Co-fired Ceramics). The designed LTCC was co-fired at $800^{\circ}C$ for 1 hour after lamination at $70^{\circ}C$ under 3000 psi for 30 minutes. $SnO_2$ sol was prepared by a hydrothermal method at $200^{\circ}C$ for 3 hours. Tin chloride and ammonium carbonate were used as raw materials and the ammonia solution was added to a Teflon jar. 20 droplets of $SnO_2$ sol were deposited onto a LTCC sensor element and this was heat treated at $600^{\circ}C$ for 5 hours. The gas sensitivity ($S\;=\;R_a/R_g$) values of the $SnO_2$ sensor and 0.04 wt% Pd-added $SnO_2$ sensor were measured. The 0.04 wt% Pd-added $SnO_2$ sensor showed higher sensitivity (S = 8.1) compared to the $SnO_2$ sensor (S = 5.95) to 200 ppm $CH_3COCH_3$ at $400^{\circ}C$.

• 대한환경공학회지
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• 제27권1호
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• pp.36-42
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• 2005

2실 구조의 바이폴라막 전기투석(EDBM) 공정을 이용하여 황산암모늄으로부터 황산과 암모니아수를 제조하기 위한 연구를 수행하였다. 황산암모늄 농도가 20 wt%인 용액에 대해 전류밀도 및 농축조에서의 황산 농도를 변화시켜 가면서 전기투석을 실시하였다. 전류밀도를 $25{\sim}100\;mA/cm^2$의 범위에서 운전한 결과 전류밀도가 증가할수록 전류효율은 증가하였다. 그러나 농축조의 황산이 음이온교환막을 통해 희석조로 확산됨으로써 일반적인 탈염용 전기투석 공정에 비해 효율이 크게 떨어지는 것으로 나타났다. 또한 농축조의 황산농도가 증가할수록 음이온교환막에서 황산의 확산속도가 증가하여 전류효율은 급격히 감소하였다. 한편 전류밀도가 증가할수록 스택의 전기저항은 감소하였는데 이는 바이폴라막의 전이영역에서 높은 전기장하에서 물이 분해되면서 발생하는 주울열에 기인하는 것으로 해석된다. 실험 결과 2실 구조의 EDBM 공정을 통해 황산암모늄으로부터 황산과 암모니아수를 생산하기 위해서는 전류효율과 전기저항 측면에서 높은 전류밀도로 운전하는 것이 효과적인 것으로 나타났다. 그러나 실제 공정에 적용되기 위해서는 전류효율을 높이면서 농축조의 황산농도를 높일 수 있는 연구가 추가적으로 진행되어야 할 것으로 판단되었다.

• Journal of Applied Biological Chemistry
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• 제43권2호
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• pp.86-93
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• 2000

An experiment was conducted to obtain the quantitative data on the transformation and loss of applied urea-N in waterlogged soil columns. The soil columns were pre-incubated for 35 days to develop oxidized and reduced soil conditions prior to urea application. After urea application at the rate of $150kg\;N\;ha^{-1}$(29.5 mg N), the amounts of nitrogen which were volatilized, leached, and remained in soil column were measured during 38 days of incubation period. On 2 and 4 days of incubation, 54.1%(15.9 mg N) and 98.4%(29.0mg N) of the applied urea was hydrolyzed, respectively. Most of the applied urea was completely hydrolyzed within 6 days. After urea application, the rates of ammonia volatilization were increased with the floodwater pH when the floodwater pH were higher than 7.0. The maximum rate of ammonia volatilization was $0.3mg\;d^{-1}$ when pH of the floodwater showed maximum value of 7.6. The total amount of volatilized nitrogen was 6.1% (1.8mg N) of the applied urea-N. A 63.2 % (18.6mg N) of the applied urea was remained in soil as $NH_4{^+}-N$ and 28.0% (8.2mg N) of the applied urea was leached as $NH_4{^+}-N$ at the end of the incubation. Amount of $NO_3{^-}-N$ in soil was smaller than 2.0 mg throughout the incubation period. The total amount of $NO_3{^-}-N$ leached was very small, which value was 1.8 mg. It suggested that nitrification process was not significant in waterlogged soil column of this study due to high infiltration rate of urea solution applied to the soil column. Therefore only small amount of $NO_3{^-}-N$ was lost by denitrification and leaching process.