• 한국가스학회지
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• 제27권3호
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• pp.19-26
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• 2023

수소는 화석연료를 대체할 수 있는 COx-free 에너지원으로 사용량은 지속적으로 증가할 것이다. 수소는 단위 질량당 에너지 함량이 높으나, 낮은 저장 밀도와 장기 저장의 어려움으로 저장 및 운송에 한계가 존재한다. 반면, 암모니아는 단위 부피당 저장용량이 크고, 비교적 액화가 용이하여 대용량 수소를 저장 및 운송할 수 있는 수소 운반체로 주목받고 있다. 암모니아 분해를 통한 수소 생산 반응은 흡열반응으로 공정의 효율성 및 경제성을 위해 저온 활성이 우수한 촉매 개발이 요구된다. 본 연구에서는 활성금속 Ni의 고분산 담지를 위해 넓은 비표면적의 제올라이트를 지지체로 사용하였으며, 제올라이트 종류(5A, NaY, ZSM5)에 따른 특성(기공구조, 양이온, Si/Al-비)이 촉매 활성 및 반응 특성에 미치는 영향을 확인하였다. 5A 제올라이트는 표면, 기공, 구조체 내에 Ni 을 고분산 담지를 가능하게 하였으며, 낮은 Si/Al-비로 인한 풍부한 산점은 암모니아 흡착을 증가시켰다. 또한, 지지체에 포함된 Na과 Ca 양이온으로 인한 중간-염기점은 질소 탈착속도를 향상시켰다. 따라서, 15wt%Ni/5A 촉매는 강한 금속-지지체 상호작용과 중간-염기점을 통한 질소 탈착 속도 향상으로 가장 우수한 암모니아 전환율과 높은 수소 생성율 23.5 mmol/g_cat·min (30,000 mL/g_cat·h, 600 ℃)을 보였다.

• 한국응용과학기술학회지
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• 제22권2호
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• pp.168-174
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• 2005

Aluminum tri-butoxide was mixed with the water/ethanol solution and then chloroplatinic acid was added to the solution. The solution was dried at $100^{\circ}C$ for 15hrs to remove the solvent and water then it was calcined at $500^{\circ}C$. The catalyst was activated with a gas mixture. During the activation, the temperature was increased from $150^{\circ}C$ to $500^{\circ}C$. The necessary amount of urea was dissolved in 50mL water and injected. Aqueous urea solution was then mixed with the feed gas stream. At low temperatures, nitrogen containing compounds of urea decomposition are used as reductants in the reducton of $NO_X$. However at high temperatures the nitrogen containing compounds are oxidized to NO and $NO_2$ by oxygen instead of being used in the reduction. The activity of the catalyst was dependent on urea concentration in the feed stream when there was not adequate water vapor in the feed. The maximum conversion was shifted from $250^{\circ}C$ to $150^{\circ}C$ when water concentration was increased from 2 to 17%. It seems that the maximum temperature shifts to lower temperatures because the hydrolysis rate of HNCO increases with water, resulting in higher amounts of $NH_3$.

• 대한화학회지
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• 제7권1호
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• pp.1-5
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• 1963

The thermal decomposition process of ammonium paratungstate $5(NH_4)_2O{\cdot}12WO_3{\cdot}5H_2O$ was analysed by the methods of thermogravimetric analysis, differential thermal analysis, quantitative analysis of the ammonia which is released during heating and X-ray powder diffraction in air and in vacuo. There are several endothermic peaks which indicate release of ammonia and exothermic peaks which indicate crystal growth and oxidation of decomposed prodects in air. After water is driven off the ammonia is released at intervals corresponding to the endothermic peaks. The highest temperature at which ammonia is released is about $420^{\circ}C$ in air and $480^{\circ}C$ in vacuo. In air the crystal structure of paratungstate is conserved up to a temperature of $300^{\circ}C$ at which the remaining ammonia is about 4 mols. At $320^{\circ}C$ the remaining ammonia becomes less than 2 mols and the paratungstate structure changes into the amorphous state. After that ${\gamma}$ oxide is produced and is oxidized to ${\alpha}$ oxide in the temperature range of 400-$500^{\circ}C$ in air. In vacuo however the endothermic peaks and structural changes occur at lower temperatures and the structure of ${\gamma}$ oxide is conserved up to temperatures higher than $500^{\circ}C$.

• 한국대기환경학회:학술대회논문집
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• 한국대기환경학회 2001년도 추계학술대회 논문집
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• pp.295-296
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• 2001

동물 축사, 폐수 및 하수처리장, 피혁공장, 생선처리시설 등에서 주로 발생하는 암모니아(NH$_3$) 및 트리메틸아민(($CH_3$)$_3$N)과 같은 악취 물질 제거에 대한 많은 연구가 진행되고 있다. 악취 물질에 대한 처리 기술에는 직접 산화법, 고온 연소법, 효소분해법, 흡착법, 촉매 산화법, 플라즈마 제거법 등과 같은 악취 물질을 분해 제거하는 방법과 단순히 악취를 은폐시키는 마스킹법이 있다. (중략)

• 한국농공학회지
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• 제43권6호
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• pp.143-153
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• 2001

Hog manure amended with sawdust (moisture 56~60% wet basis, C/N 19-21) was composted in pilot-scale vessels using continuous aeration(CA) and intermittent aeration(IA) for 3 and 4 weeks. In two subsequent runs of the same duration, composts resulting from each of the first runs were used as a biofilter on the exhaust gas from newly composting material. Conditions between each of these paired sets appeared to be similar. Ammonia was released from the biofilter material during the first week of stabilization while the compost produced ammonia after the first week of composting. In both cases substantial absorption, 61~96 %, of ammonia production from the composting raw material was achieved in the stabilizing material during the final weeks of operation and indicates the use of the stabilizing hog manure/sawdust compost as a biofilter can reduce ammonia emissions. Total $NH_3-N$ emissions during run 2 in IA was less than 2/3 of those in CA. Dry solids loss for the stabilized compost (6~8 weeks) was 19~46%.

• 공업화학
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• 제8권3호
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• pp.430-437
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• 1997

핵연료 분말제조 공정에서 발생하는 여액중의 미량 우라늄과 과산화수소 용액을 반응시켜 uranyl-peroxide 화합물을 제조하였다. 여액에 $CO_3{^{2-}}$가 공존할 경우에는 용해되어 있는 $UO_2{^{2+}}$가 침전되지 않기 때문에, 여액을 $98^{\circ}C$로 가열하여 $CO_3{^{2-}}$를 우선 제거하였다. Uranyl-peroxide 화합물 제조시 최적조건으로는 암모니아 가스로 여액의 pH를 9.5로 조절한 후 과량의 과산화수소 용액을 10ml/lit.-filtrate로 첨가하여 1시간 ageing시킬 때이며, 처리후 여액중의 우라늄농도는 3ppm 이하로 나타났다. 제조된 uranyl-peroxide 화합물을 FT-IR, X-ray, TG 및 화학분석 등을 통해 분석한 결과 화합물의 조성은 $UO_4{\cdot}2NH_4F$로 나타났으며, 초기 생성된 $1{\sim}2{\mu}m$의 $UO_4{\cdot}2NH_4F$ 입자들은 반응온도 $60^{\circ}C$ 및 pH 9.5에서 약 $4{{\mu}m}$로 성장하였다. 최적조건에서 제조된 입자들의 고/액 분리효율은 pH의 증가 및 반응온도의 상승에 따라 증가하는 경향으로 나타났다. 한편, 제조된 입자들의 결정형태는 SEM 및 XRD에 의한 분석결과 octahedral 형태로 나타났으며, 이 분말을 공기분위기에서 $650^{\circ}C$까지 열분해한 결과 $U_3O_8$으로 판명되어 핵연료 분말제조 공정으로 재순환이 가능하였다.

• Korean Chemical Engineering Research
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• 제60권1호
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• pp.159-168
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• 2022

MoO₃ 비율을 10-50 중량비로 변화하여 제조한 Mo-Al 복합 산화물 상에서 소성 후 승온 질화반응을 통하여 얻은 Mo-Al 질화물 상에서 암모니아 분해반응에서의 촉매 활성을 검토하였다. 제조된 촉매의 물리·화학적 특성을 알아보기 위하여 N₂ 흡착분석, X-선 회절분석(XRD), X-선 광전자분석법(XPS), 수소 승온환원(H₂-TPR), 투과전자현미경(TEM) 분석을 수행하였다. 600 ℃에서 소성 후 Mo-Al 복합산화물은 γ-Al₂O₃와 Al₂(MoO₄)₃ 결정상을 나타냈으며 질화반응 후의 질화물은 비정형 형태를 보여주었다. 질화반응 후의 비표면적은 MoO₃의 위상전환반응에 의해 Mo 질화물 형성으로 인해 증가하였으며, Mo 질화물이 γ-Al₂O₃에 담지된 형태를 보여주었다. 암모니아 분해반응에서의 촉매 활성은 40 wt% MoO₃가 가장 좋은 활성을 보여주었고, 질화반응 시간이 증가함에 따라 활성이 증가하였으며 이에 따라 활성화에너지 감소 효과를 나타냈다.

• 자원리싸이클링
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• 제13권5호
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• pp.45-50
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• 2004

탄화철을 합성하는 공정을 수소($H_2$) 환원과 $CO-H_2$ 혼합가스에 의한 탄화의 2단계 과정으로 나누어서 수행했다. 환원종료 후 미량의 암모니아 가스를 첨가하여 환원철의 표면을 개질한 후, 탄화시간 경과별 탄화상태를 C/S 분석기(Low C/S determinator), 뫼스바우어 분광 분석기(Mossbauer spectroscopy), XRD(X-ray diffraction patterns), SEM(Scanning electron microscopy), TEM(Transmission electron microscopy), XPS(Photoelectron spectroscopy), 및 라만분광기 (Raman spectroscopy)를 사용하여 조사하였다. 연구결과, 미량의 암모니아가스로 환원철 표면을 개질함으로써 탄화철의 분해 및 유리탄소의 석출을 방지할 수 있을 뿐만아니라 6.68wt% 이상 10wt% 까지 탄소가 과고용된 상태에서도 분해되거나 유리탄소를 석출하지 않고 안정상태를 유지하였다. 이러한 결과로부터 철(Fe)과 세멘타이트(cementite, $Fe_3C$)가 혼합되지 않고 고탄화철(SIC, super iron carbide)인 Fe5C2 상태의 안정한 단일상을 얻는데 성공하였다.

• Journal of the Korean Wood Science and Technology
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• 제52권3호
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• pp.205-220
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• 2024

Various polylactic acid (PLA) blends were reinforced with untreated or silane-treated micro-sized cellulose fiber (MCF), successfully prepared as 3D printing filaments and then printed using a fused filament fabrication (FFF) 3D printer. In this study, we focused on developing 3D-printed MCF/PLA composites through silane treatment of MCF and investigating the effect of silane treatment on the various properties of FFF 3D-printed composites. Fourier transform infrared spectra confirmed the increase in hydrophobic properties of silane-treated MCF by showing the new absorption peaks at 1,100 cm^-1, 1,030 cm^-1, and 815 cm^-1 representing C-NH₂, Si-O-Si, and Si-CH₂ bonds, respectively. In scanning electron microscope images of silane-treated MCF filled PLA composites, the improved interfacial adhesion between MCF and PLA matrix was observed. The mechanical properties of the 3D-printed MCF/PLA composites with silane-treated MCF were improved compared to those of the 3D-printed MCF/PLA composites with untreated MCF. In particular, the highest tensile and flexural modulus values were observed for S-MCF10 (5,784.77 MPa) and S-MCF5 (2,441.67 MPa), respectively. The thermal stability of silane-treated MCF was enhanced by delaying the initial thermal decomposition temperature compared to untreated MCF. The thermal decomposition temperature difference at T₉₅ was around 26℃. This study suggests that the effect of silane treatment on the 3D-printed MCF/PLA composites is effective and promising.

• 한국세라믹학회지
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• 제28권9호
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• pp.667-674
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• 1991

In this study, Kaolin was carbonized at 1300~175$0^{\circ}C$ and its constituent mineral change was investigated. Carbonized kaolin at 1$650^{\circ}C$ was mixed with metallic silicon, formed and nitrified at 135$0^{\circ}C$ in N2-NH3 atmosphere. Properties of this product such as porosity, bulk density, MOR, nitrization rate and oxidation resistence were measured, and its mineralogical changes were investigated by XRD. The results were as follows; 1) $\beta$-SiC was initially synthesized at 150$0^{\circ}C$, and its amount was continuously increased with reaction temperature to 1$700^{\circ}C$. 2) At 1$600^{\circ}C$, mullite was rapidly decomposed and the amounts of $\beta$-SiC and $\alpha$-Al2O3 were increased simultaneously. 3) By adding alkali to kaolin, the decomposition temperature of mullite was dropped approximately 10$0^{\circ}C$, but the amount of $\alpha$-SiC was increased. 4) The highest values of their nitrization rate and MOR were obtained at the specimen of 35 wt% metallic silicon in nitrization reaction. 5) It seems that increment of $\alpha$-Si3N4 and $\alpha$-Al2O3 phase during nitrization was due to the decomposition of Al4SiC4 existed in carbonized kaolin. 6) Si3N4 bonded SiC-Al2O3 composite were fabricated from kaolin at relatively low temperature (135$0^{\circ}C$).