• 제목/요약/키워드: Material Decomposition

검색결과 634건 처리시간 0.035초

바이오디젤 혼합물의 함량변화에 따른 열적 특성에 대한 실험적인 연구 (Experimental Study on the Thermal Characteristics According to the Content Change of Biodiesel Mixture)

  • 김주석;고재선
    • 한국재난정보학회 논문집
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    • 제19권3호
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    • pp.532-544
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    • 2023
  • 연구목적: 신규로 사용되는 바이오연료를 기존 연료와 혼합하여 사용하는 경우 발생하는 위험성과 물성 변화를 열분석 방법(DSC, TGA)을 사용하여 화학 화재의 원인물질의 위험성을 확인하고, 평가할 방법과 그에 따른 물질의 위험성 관련 데이터를 확보함으로써 화재 원인 감식과 감정에 활용하기 위함이다. 연구방법: 본 실험에 사용된 연구 방법으로는 시차주사열량계(DSC : Differential Scanning Calorimeter)에 의하여 피크의 위치, 모양, 개수, 피크의 면적으로부터 열량 변화의 정량적인 정보를 통하여 열유속 차이(Difference in heat flux)를 측정하였고, 열중량분석(TGA : Analyzer)을 시행함으로써 특정한 온도에서 분해열 등에 의해 발생한 무게 변화를 연속적으로 측정하였다. 연구결과: 먼저 열 유속의 그래프에서 물질의 끓는점과 물질이 가지고 있는 고유 특성치 또는 분해에 필요한 에너지를 확인할 수 있다. 둘째 바이오디젤의 함량이 증가할수록 많은 피크를 확인 할 수 있었다. 셋째 비점이 낮은 물질들이 함유하고 있다는 것을 분석 결과로 확인할 수 있었다. 결론: 현재 새로운 에너지원으로 사용되고 있는 바이오디젤의 위험성을 다양한 물리·화학적 분석기법(DSC+TGA)을 통하여 사용함으로써 물질의 물적 위험성을 평가할 수 있음을 보여주었다. 아울러 본 연구의 시험방법별 차이의 비교와 실험에 대한 노하우를 축적하고 활용한다면 향후 위험물의 물성 연구와 물질 위험성 평가 연구에 있어 도움이 되리라 기대한다.

진공튜브 속에서 분해하는 리튬암모니아 솔루션의 열전효율 향상 (Thermoelectric Efficiency Improvement in Vacuum Tubes of Decomposing Liquid Lithium-Ammonia Solutions)

  • 이정윤;김미애;심규철;김지범;전준현
    • Korean Chemical Engineering Research
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    • 제51권3호
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    • pp.358-363
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    • 2013
  • 순수한 리튬-암모니아(Li-$NH_3$) 솔루션의 생성은 진공 상태에서 가능하지만, 고효율 열전전력을 얻기 위한 안정적이고 신뢰성 있는 분해에 대한 문제가 아직 남아있다. 본 논문은 Li-$NH_3$ 솔루션의 열전변환 효율을 향상시키기 위한 새로운 방법을 다루었다. 제안된 방법은 Li-$NH_3$ 솔루션의 합성과 분해를 위해 'U' 형태의 파이렉스 진공 튜브를 사용하였다. 튜브 상부에는 기존 'U' 형태의 파이렉스 진공 튜브의 두 다리를 연결하는 기체의 이동통로가 있는데, 이는 고온부(Hot side)에서 분해가 진행될 때 $NH_3$ 기화에 따른 양단의 내부압력 불균형을 방지하는 역할을 한다. 열전 실험결과, 'U' 형태 튜브 속에서 솔루션 반응은 기존 'U' 형태에 비해 매우 안정적이고 효율적으로 이루어졌으며, 결과적으로 열전변환 효율이 향상됨을 보였다. 또한, 제안 방식은 장시간에 걸친 고효율 열전 발전을 위해 튜브 속에서 합성과 분해가 순환되는 가역반응을 제공함이 입증되었다.

Evaluating Soil Carbon Changes in Paddy Field based on Different Fraction of Soil Organic Matter

  • Seo, Myung-Chul;Cho, Hyeon-Suk;Kim, Jun-Hwan;Sang, Wan-Gyu;Shin, Pyeong;Lee, Geon Hwi
    • 한국토양비료학회지
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    • 제48권6호
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    • pp.736-743
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    • 2015
  • Organic matter plays important roles in soil ecosystem in terms of carbon and nitrogen cycles. Due to recent concerns on climate change, carbon sequestration in agricultural land has become one of the most interesting and debating issues. It is necessary to understand behavior of soil carbon for evaluating decomposition or sequestration of organic matter and analyzing potential carbon decomposition pattern about the kinds of organic matter sources to cope with well. In order to evaluate decomposition of soil carbon according to organic material during cultivating rice in paddy field, we treated organic material such as hairy vetch, rice straw, oil cake fertilizer, and manure compost at $50{\times}50{\times}20cm$ blocks made of wood board, and analyzed carbon contents of fulvic acid and humic acid fraction, and total carbon periodically in 2013 and 2014. Soil sampling was conducted on monthly basis. Four Kinds of organic matter were mixed with soil in treatment plots on 2 weeks before transplanting of rice. The treatment of animal compost showed the highest changes of total carbon, which showed $7.9gkg^{-1}$ in May 2013 to $11.6gkg^{-1}$ in October 2014. Fulvic acid fraction which is considered to easily decompose ranged from 1 to $2gkg^{-1}$. Humic acid fraction was changed between 1 to $3gkg^{-1}$ in all treatments until organic material had been applied in 2014. From May to August in the second year, the contents of humic acid fraction increased to about $4gkg^{-1}$. The average of humic fraction carbon at treatments of animal compost was recorded highest among treatments during two years, $2.1gkg^{-1}$. The treatment of animal compost has showed the lowest ratio of fulvic acid fraction, humic acid fraction compared with other treatments. The average ratio of fulvic fraction carbon in soil ranged from 16 to 20%, and humic fraction carbon ranged from 19 to 22%. In conclusion, animal compost including wood as bulking agent is superior in sequestrating carbon at agricultural land to other kinds of raw plant residue.

카바졸을 포함하는 청색 OLED 재료의 합성 (Synthesis and Characterization of Carbazole Derivate for Blue light Emitting Material)

  • 신민기;박현태;장상훈;고혜진;장재완;김윤희;권순기
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2010년도 하계학술대회 논문집
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    • pp.58-58
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    • 2010
  • We designed and synthesized DFPCE blue emitting materials by Mc Murry coupling reaction in order to improve the device efficiency and stability. The structure was confirmed by $^1H$-NMR. The physical properties were characterized by differential scanning calorimetry, thermogravimetric analysis, UV-vis, photoluminescence spectrum and cyclic voltammetry. The decomposition temperature of the material, which correspond to a 5% weight loss upon heating, is $513.58^{\circ}C$. The photoluminescence (PL) spectrum of DFPCE exhibited blue emission at 425 nm in chloroform solution and 462 nm in film.

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금속유기분해법으로 제조한 니켈 망가나이트 박막의 구조적 특성 (Structural Properties of Nickel Manganite Thin Films Fabricated by Metal Organic Decomposition)

  • 이귀웅;전창준;정영훈;윤지선;남중희;조정호;백종후;윤종원
    • 한국전기전자재료학회논문지
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    • 제27권4호
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    • pp.226-231
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    • 2014
  • Thin thermistor films of solutions with nickel and manganese oxides were prepared by metal-organic decomposition (MOD). The structural properties of the thin films were investigated as a function of annealing temperature. Field emission scanning electron microscope (FE-SEM) results indicated that the thin films had a thin thickness, smooth and dense surface. The crystallization temperature of $414.9^{\circ}C$ was confirmed from thermogavimetric-differential thermal analysis (TG-DTA) curve. A single phase of cubic spinel structure was obtained for the thin film annealed from $700^{\circ}C$ to $800^{\circ}C$, which was confirmed from the X-ray diffraction (XRD). From the selected area electron diffraction (SAED) in high resolution transmission electron microscope (HRTEM), the nano grains (2~3 nm) of spinel phase with (311) and (222) planes were detected for the thin film annealed at $500^{\circ}C$, which could be applicable to read-out integrated circuit (ROIC) substrate of the uncooled microbolometer with low processing temperature.

제조공정에 따른 MnO2산화물 전극의 전기화학적 특성 (Electrochemical Characteristics of MnO2 Electrodes as a function of Manufacturing Process)

  • 김현식;이해연;허정섭;이동윤
    • 한국전기전자재료학회논문지
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    • 제17권5호
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    • pp.486-491
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    • 2004
  • Dimensionally stable anode(DSA) can be used for the hydro-metallurgy of non-ferrous metals like as Zn, and the electrolysis of sea water. MnO$_2$ electrode satisfies the requirements of DSA, and has a good cycle life and a low overpotential for oxygen evolution. MnO$_2$ electrodes based on Ti matrix were prepared by using thermal decomposition method and also MnO$_2$ was coated on Ti and Pb matrix with DMF and PVDF compositions. The MnO$_2$ electrodes prepared by thermal decomposition method had very weak adhesive strength onto Ti matrix and MnO$_2$ layer was removed out so that electrochemical properties for MnO$_2$ were not investigated. The viscosity of solvent used as a binder of MnO$_2$ Powder increased with the increasing PVDF contents. The thickness of the MnO$_2$ layer on Pb matrix in DSA, which was prepared with 5 times dipping at the solution mixed with PVDF : DMF = 1 : 9, was 150${\mu}{\textrm}{m}$. When the ratio of PVDF to MnO$_2$ was lower than 1 : 6, the Pb electrode didn't show any reaction irrespective of the concentrations of DMF. However, When the ratio of PVDF to MnO$_2$ was higher than 1: 6, the Pb electrode showed constant current reactions and homogeneous cyclic voltammetry even though at a high cycle. The reason for the high current and homogeneous cyclic voltammetry is the good catalytic reactions of MnO$_2$ powder in electrode.

Modeling and numerical simulation of electrostrictive materials and structures

  • Pechstein, Astrid;Krommer, Michael;Humer, Alexander
    • Smart Structures and Systems
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    • 제30권3호
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    • pp.221-237
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    • 2022
  • This paper is concerned with nonlinear modeling and efficient numerical simulation of electrostrictive materials and structures. Two types of such materials are considered: relaxor ferroelectric ceramics and electrostrictive polymers. For ceramics, a geometrically linear formulation is developed, whereas polymers are studied in a geometrically nonlinear regime. In the paper, we focus on constitutive modeling first. For the reversible constitutive response under consideration, we introduce the augmented Helmholtz free energy, which is composed of a purely elastic part, a dielectric part and an augmentation term. For the elastic part, we involve an additive decomposition of the strain tensor into an elastic strain and an electrostrictive eigenstrain, which depends on the polarization of the material. In the geometrically nonlinear case, a corresponding multiplicative decomposition of the deformation gradient tensor replaces the additive strain decomposition used in the geometrically linear formulation. For the dielectric part, we first introduce the internal energy, to which a Legendre transformation is applied to compute the free energy. The augmentation term accounts for the contribution from vacuum to the energy. In our formulation, the augmented free energy depends not only on the strain and the electric field, but also on the polarization and an internal polarization; the latter two are internal variables. With the constitutive framework established, a Finite Element implementation is briefly discussed. We use high-order elements for the discretization of the independent variables, which include also the internal variables and, in case the material is assumed incompressible, the hydrostatic pressure, which is introduced as a Lagrange multiplier. The elements are implemented in the open source code Netgen/NGSolve. Finally, example problems are solved for both, relaxor ferroelectric ceramics and electrostrictive polymers. We focus on thin plate-type structures to show the efficiency of the numerical scheme and its applicability to thin electrostrictive structures.

음식물쓰레기 퇴비화에서 혼합물 특성이 퇴비화에 미치는 영향 (An Influence of Mixing Material Characteristics on the Composting of Food Waste)

  • 정준오;권혁구;이장훈
    • 한국환경보건학회지
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    • 제28권5호
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    • pp.22-27
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    • 2002
  • The composting practice has been recognized as the most popular way of controlling food waste and many attempt have been made in the field to establish more efficient and economical process. Some of the efforts are mixing cured compost with sawdust as alternative bulking agent, seeding commercially produced microorganism and/or combination of above. However, verification of such efforts is often restricted because of either the lack of engineering consideration on the limitation of composting facility scales. In this study, the effect of mixing materials in food waste composting was investigated by controlling the combination and the mixing ratio of them. When the cured compost was mixed with saw dust. the decomposition of organic material was proven to be more active by observing the compost temperature, the oxygen (O$_2$) consumption, and the cumulative carbon dioxide ($CO_2$) profile. However, the quantity of compost mix-ing seemed not to influence the reaction as long as the minimum required amount was mixed. The feeding of com-mercially produced microorganism had a tendency to prolong the thermophilic stage, which helped to increase the decomposition but it resulted in composting period. Regardless of the composting condition, bacteria and actinomycetes increased in population as the reaction approached to the end. The population of bacteria and actinomycetes were rel-atively higher than those of fungi and yeast throughout the reaction.

대기 중 휘발성 유기화합물의 광산화 공정 및 광촉매산화 공정의 처리효율 비교 (A Study on the Photolytic and Photocatalytic Oxidation of VOCs in Air)

  • 서정민;정창훈;최금찬
    • 한국대기환경학회지
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    • 제18권2호
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    • pp.139-148
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    • 2002
  • Both UV Photolysis and Phtocatalytic Oxidation Processing are an emerging technology for the abatemant of Volatile Organic Compounds (VOCs) in atmospheric -pressure air streams. However, each process has some drawbacks of their own. The former is little known as an application for air pollution treatment, so it has been a rare choice in the field. Therefore we have to do more experiment and study for its application for treatment of VOCs. Although the latter has been used in the industrial fields, it still has a difficulty in decomposing high concentrations of VOCs. To solute these problems, we have been studying simultaneous application of those two technologies. We have studied the effects of background gas composition and gas temperature on the decomposition chemistry. It has shown that concentration of TCE and B.T.X., diameter of reactor, and wavelength of lamp have effects on decomposition efficiency. When using Photolysis Process only, the rates of fractional conversion of each material are found at TCE 79%, Benzene 65%, Toluene 68%, Xylene 76%. In case of Photocatalytic Oxidation Process only, the rates of fractional conversion decreased drastically above 30 ppm. When there two methods were combined, the rates of fractional conversion of each material are enhanced such as TCE 93%, Benzene 75%, Toluene 81%, Xylene 90%. Therefore, we conclude that the combination of Photolysis-Photocatalytic Oxidation process is more efficient than each individual process.

Study on Reactive Non-thermal Plasma Process combined with Metal Oxide Catalyst for Removal of Dilute Trichloroethylene

  • Han Sang-Bo;Oda Tetsuji;Park Jae-Youn;Park Sang-Hyun;Koh Hee-Seok
    • 한국전기전자재료학회논문지
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    • 제19권3호
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    • pp.292-300
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    • 2006
  • In order to improve energy efficiency in the dilute trichloroethylene removal using the nonthermal plasma process, the barrier discharge treatment combined with manganese dioxide was experimentally studied. Reaction kinetics in this process was studied on the basis of final byproducts distribution. Decomposition efficiency was improved to about $99\;\%$ at the specific energy of 40 J/L with passing through manganese dioxide. C=C ${\pi}$ bond cleavage of TCE substances gave DCAC, which has the single bond of C-C through oxidation reaction during the barrier discharge plasma treatment. Those DCAC were broken easily in the subsequent catalytic reaction due to the weak bonding energy about $3{\sim}4\;eV$ compared with the double bonding energy in TCE molecules. Oxidation byproducts of DCAC and TCAA from TCE decomposition are generated from the barrier discharge plasma treatment and catalytic surface chemical reaction, respectively. Complete oxidation of TCE into COx is required to about 400 J/L, but $CO_2$ selectivity remains about $60\;\%$.