• Title/Summary/Keyword: thermal pyrolysis

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The Effect of Pyrolysis Pressure on Combustion Reactivity of Coal Char (열분해 압력이 석탄 촤의 연소반응성에 미치는 영향)

  • Park Ho Young;Kim Young Ju;Kim Tae Hyung;Seo Sang Il
    • Journal of Energy Engineering
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    • v.14 no.1
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    • pp.1-10
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    • 2005
  • The combustion reactivity of char depending on the pyrolysis pressure was investigated with Pressurized Thermogravimetric Analyser. The amounts of volatiles released at pyrolysis pressure of 1, 8 and 15 atm were, first, measured with Alaska, Adaro and Denisovsky coals. Reactivities of chars produced at var-ious pyrolysis pressure were evaluated at atmospheric pressure and 500℃, and analysed in terms of char crystal structure, surface area, pore characteristics and chemical composition of char. Finally, the combustion reactivities of three chars were examined at pressure of 1 atm, 8 atm and 15 atm. From this study, it was recognized that the amount of volatiles released decreases with increase in pyrolysis pressure, and reaction rate of char produced at higher pyrolysis pressure was lower than that at lower pyrolysis pressure. It might be resulted from the difference in char surface area and pore characteristics rather than char crystal structure and chemical characteristics. At 15 atm, kinetic parameters of Alaska char were obtained with the grain model, and these were 56.8 KJ/mole for activation energy and 222.34 (1/min) for frequency factor.

Full Scale Study on The Optimum Conditions for Disposal of Sewage Sludge Cake by Using Continual Thermal Wind Dryer and Pyrolysis (연속적 열풍건조/열분해 Full Scale 장치를 이용한 하수슬러지 케익 처분을 위한 최적조건 연구)

  • Ha, Sang-An
    • Journal of the Korea Organic Resources Recycling Association
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    • v.16 no.3
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    • pp.29-37
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    • 2008
  • The objective of this research is to evaluate the optimum treatment methods for disposal sludge cake at different temperatures and periods of time. The disposal dehydrated sewage cake used in this study was obtained from N wastewater treatment plant in the P City. This system consists of continuous conveyer thermal dryer and pyrolysis. The continual conveyer thermal dryer was operated to evaluate the optimum conditions with temperature settings, ranges from 130 to $180^{\circ}C$, loading rates of 650~750 kg/hr and operating times of 110~120 minutes. The continual pyrolysis was also operated to evaluate the optimum conditions with temperature settings, ranges from 650 to $750^{\circ}C$, loading rates of 100~158 kg/hr and operating times of 20~40 minutes. The sewage sludge cake has a moisture content of 78~80% (wt) which decreased up to 1~3%(wt) resulted in breaking of cell wall after operating the continuous conveyer thermal dryer and pyrolysis. Important parameters which were operating times, moisture contents, loading rates, conveyer velocities and rotary velocities effects on the thermal kinetics and dynamics were investigated to evaluate the optimum conditions for the continual thermal dryer and pyrolysis.

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COMBUSTION CHARACTERISTICS OF WASTE-PYROLYSIS GASES IN AN INTERNAL COMBUSTION ENGINE

  • Shudo, T.;Nagano, T.;Kobayashi, M.
    • International Journal of Automotive Technology
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    • v.4 no.1
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    • pp.1-8
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    • 2003
  • Wastes such as shredder dust of disposed vehicles can be decomposed into low calorific flammable gases by Pyrolysis gasification. A stationary electric Power generation using an internal combustion engine fuelled with the waste-pyrolysis gas is an effective way to ease both waste management and energy saving issues. The waste-pyrolysis gas mainly consists of H$_2$, CO, $CO_2$ and $N_2$. The composition and heating value of the gas generated depend on the conversion process and the property of the initial waste. This research analyzed the characteristics of the combustion and the exhaust emissions in a premixed charge spark ignition engine fuelled with several kinds of model gases, which were selected to simulate the pyrolysis-gases of automobile shredder dusts. The influences of the heating value and composition of the fuel were analyzed parametrically. Furthermore, optical analyses of the combustion flame were made to study the influence of the fuel's inert gas on the flame propagation.

$MoSi_2$/SiC Ceramic Composites Prepared by Polymer Pyrolysis (고분자 열분해에 의한 $MoSi_2$/SiC 세라믹 복합체)

  • 김범섭;김득중;김동표
    • Journal of the Korean Ceramic Society
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    • v.37 no.8
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    • pp.805-810
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    • 2000
  • The formation, microstructure and properties of MoSi2/SiC ceramic composites by polymer pyrolysis were investigated for the application of heating element material. Polymethylsiloxanes were mixed with Si, SiC, MoSi2 as filler and ceramic composites prepared by pyrolysis in N2 atmosphere at 1320~145$0^{\circ}C$ were studied. Dimensional change, density variation and phases were analyzed and correlated to the resulting material properties. Microstructures of ceramic composite prepared by polymer pyrolysis were composed of MoSi2, SiC and silicon oxycarbide glass matrix. Depending on the pyrolysis conditions, ceramic composites with a density of 86~90 TD%, a fracture strength of 213~284 MPa, a thermal expansion coefficient of 4~7$\times$10-6 were obtained. The electrical resistivity of the specimen decreased with increasing of temperature up to 50$0^{\circ}C$.

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Formation of Tetra-Chlorinated Dibenzo-p-dioxins and Their Thermal Decomposition Products from Pyrolysis Reaction of Tri-Chlorophenates

  • 홍종기;박종세;김강진
    • Bulletin of the Korean Chemical Society
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    • v.17 no.4
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    • pp.334-338
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    • 1996
  • Tetra-chlorodibenzo-p-dioxins (tetra-CDDs) were prepared by microscale pyrolysis of trichlorophenates. During the pyrolysis reaction, tri-, di-, and mono-CDDs were also formed by the thermolysis of tetra-CDDs. The dechlorination pathways of tetra-CDDs were suggested for this reaction. The identification of these products was performed with capillary column gas chromatography-mass spectrometry.

Simulation of Physical Chemistry Phenomena Inside a Naturally Smoldering Cigarette (자연 연소중인 궐련내에서 일어나는 물리화학적 현상의 시뮬레이션)

  • 오인혁;김기환;정경락
    • Journal of the Korean Society of Tobacco Science
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    • v.20 no.1
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    • pp.87-94
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    • 1998
  • After we made the computer source code with mathematical model of Muramatsu et al. that was expressed by the set of simultaneous first-order ordinary differential equations in evaporation-pyrolysis zone of cigarette, we simulated the distribution profiles of temperature and density of flue-cured tobacco. Those equations were solved numerically with the Runge-Kutta-Gill algorithm assuming step size of 0.025mm by Muramatsu at at,, but in this study the advanced algorithm of Runge-Kutta 4th Order assuming step size of 0.0005mm. The initial conditions and physical parameters of Muramatsu et at. were used for solving them. The calculated values corresponded well with results of Muramatsu et al., especially the gradient of the temperature profile increased with smoldering speed and the thickness of the evaporation-pyrolysis zone decreased with increasing of smoldering speed. On the other hand, the temperature gradient decreased with increasing of the effective thermal-conductivity value and the thickness of the evaporation-pyrolysis zone increased with the effective thermal-conductivity value.

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Effect of pyrolysis temperature on the thermal energy storage performance of sesame plant biochar (참깨 바이오차의 열분해 온도가 열에너지 저장 성능에 미치는 영향 평가)

  • Soumen Mandal;Lee, Han-Seung
    • Proceedings of the Korean Institute of Building Construction Conference
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    • 2023.11a
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    • pp.65-66
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    • 2023
  • This study is aimed to understand the effect of pyrolysis temperature on the biochar synthesis for shape stabilizing the Lauric acid (LA). Three different temperatures (350, 500, and 650 ℃) have been chosen with a soaking time of 1h for synthesizing biochars form sesame plants (SP). The structural characterizations indicate the formation of amorphous biochar at 350 ℃ whereas, a stain of graphene formation has been observed for the biochar synthesized at 500 ℃. Formation of a substantial amount of graphene has been found for the sample, synthesized at 650 ℃. Energy storage performances of the PCMs which are shape stabilized by these three biochars have been discussed in this paper.

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Thermal Degradation of High Molecular Components Obtained from Pyrolysis of Mixed Waste Plastics (혼합폐플라스틱의 열분해로부터 생성된 고분자성분의 열적분해)

  • Oh, Sea Cheon;Ryu, Jae Hun;Kwak, Hyun;Bae, Seong-Youl;Lee, Kyong-Hwan
    • Applied Chemistry for Engineering
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    • v.19 no.2
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    • pp.191-198
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    • 2008
  • The thermal degradation characteristics of high molecular components obtained from pyrolysis of mixed waste plastics have been studied by thermogravimetric analysis (TGA) and gas chromatography spectrometry (GC-MS). The kinetics of thermal degradation has been studied by a conventional nonisothermal thermogravimetric technique at several heating rates between 10 and $50^{\circ}C/min$. The dynamic thermogravimetric analysis curve and its derivative have been analyzed using a variety of analytical methods reported in the literature to obtain information on the kinetic parameters such as activation energies and reaction orders. The yields of liquid products have been monitored by batch pyrolysis reactor under various reaction temperatures and reaction times. And the characteristic of liquid products with the increase in reaction temperature has been performed by GC-MS.

Combustible gas production from waste tire pyrolysis process by thermal plasma (열플라즈마에 의한 폐타이어의 열분해 공정에서 가연성 가스 생성)

  • Choi, Kyung-Soo;Park, Dong-Wha
    • Clean Technology
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    • v.5 no.1
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    • pp.42-48
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    • 1999
  • Waste tires have both sides which are contamination and reuse concern with environmental problems. In this study, tire pyrolysis was conducted to convert combustible gases using thermal plasma. Production of combustible gases was found by gas chromatography after thermal plasma pyrolysis of waste tires without oxygen. The combustible gases consist of low molecular hydrocarbons such as $CH_4$, $C_2H_2$, $C_4H_{10}$ etc. As tire feed rate increased, the composition of $CH_4$ in the gases was increased. As plasma power increased, the composition of $C_2H_2$ was increased. $C_2H_2$ and $C_4H_{10}$ were dominant and had the ratio over 70% in the gases. On the other hand the trends of pyrolysis was characterized in the thermal plasma from the results of TG analysis which shows the currents of decomposition of the char according to the temperature.

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Pyrolytic Behavior of Propylene Glycol and glycerine (Propylene Glycol과 glycerine의 열본해 특성)

  • Lee Jae-Gon;Lee Chang-Gook;Baek Shin;Jang Hee-Jin;Kwag Jae-Jin;Lee Dong-Wook
    • Journal of the Korean Society of Tobacco Science
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    • v.27 no.1 s.53
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    • pp.31-39
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    • 2005
  • This study was conducted to evaluate the characterization of the pyrolysis products of propylene glycol(PG) and glycerine alone and together with tobacco. The weight change of the samples during the pyrolysis was measured by a thermal analyzer(STD-2960). The pyrolysis products were determined by GC/MS after pyrolysis using a curie-point pyrolyzer(CPP, $220^{\circ}C,\;420^{\circ}C,\;650^{\circ}C,\;and\;920^{\circ}C$) and a double-shot pyrolyzer(DSP, $220^{\circ}C,\;420^{\circ}C,\;650^{\circ}C,\;and\;800^{\circ}C$), respectively. The pyrolysis products from tobacco with and without the addition of PG($2\%$) and glycerine($2\%$ were assayed for its pyrolytic behavior. The results showed that a dramatic change in weight of PG and glycerine was observed at $175^{\circ}C\;and\;249^{\circ}C$, respectively. PG and glycerine showed different patterns for their pyrolysis products according to the method of pyrolysis. Namely, the change rate in pyrolysis with DSP was much higher than that of CPP at above $650^{\circ}C$. The major pyrolysis products of PG were propene, acetaldehyde, propanal, and acetol; the major pyrolysis products of glycerine were 2-propenal, 2-propenol, acetol, and acetic acid. In the pyrolysis experiments of tobacco added PG and glycerine, the pyrolysis products of PG and glycerine weren't detected additionally, except for diethyleneglycol diacetate. From these results, it can be concluded that the PG and glycerine added to tobacco would not be expected to pyrolyse extensively during smoking.