• 제목/요약/키워드: activation volume

검색결과 396건 처리시간 0.021초

물리적 활성화에 의한 PAN계 활성탄소섬유의 제조 (Preparation of PAN-based Activated Carbon Fibers by Physical Activation)

  • 임연수;김기원;정승훈;김기덕;정윤중
    • 한국세라믹학회지
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    • 제36권10호
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    • pp.1016-1021
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    • 1999
  • 활상탄소섬유는 입상 활성탄에 비해 빠른 흡 · 탈착 속도와 높은 흡착량을 갖기 때문에 흡착재, 촉매, 분자체와 같은 환경 신소재로서 큰 주목을 받고 있다. 본 연구에서는 안정화 PAN계 탄소섬유를 수증기와 CO2를 이용한 물리적 활성화에 의해 여러 등급의 활성탄소섬유를 제조하였고, 비표면적, 요오드 흡착량, 세공구조 등을 측정하였다. 수증기 활성화에서 77%의 burn-off에서 비표면적이 1019 m2/g을 나타내었고, 반면에 CO2 활성화에서는 52%의 burn-off에서 7168m2/g의 비표면적을 갖는 활성탄소섬유가 제조되었다 그러나, 비슷한 burn-off에서는 CO2로 활성화한 경우에서 세공용적이 0.37 cc/g이고, 요오드 흡착량이 1589 mg/g으로서 수증기 활성화보다 더 큰 세공용적과 요오드 흡착량을 나타내었다. 또한 제조된 활성탄소섬유의 질소 흡착등온선들은 Brunaner-Deming-Deming-Teller의 분류에 따르면 모두 type I으로 주로 미세공들로 이루어져 있음을 알 수가 있었다.

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수중기 활성화법으로 제조된 영월 석탄계 활성탄의 특성 연구 (Characterisitcs of steam activated carbon made from Youngwall coal)

  • 이송우;권태훈;나영수;최동훈;류동춘;송승구
    • 한국환경과학회지
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    • 제9권4호
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    • pp.339-343
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    • 2000
  • Activated carbons were prepared from Youngwall coal by steam activation in this study. The feasibility of the Youngwall coal to commercial activated carbon was examined. The variation of pore structures and the development of porosity in activated carbons were investigated by changing activation conditions in batch type apparatus. The values of BET surface area and adsorption capacity of iodine and methylene blue of the resulting activated carbons were obtained as high as 1,000$m^2$m^2$$/g, 900mg/g, 150$m\ell$/g, respectively. Youngwall activated carbon prepared in this study showed much higher pore volume in pore diameter over 10 than that of commercial reference activated carbon(Ningxia Taihua ZJ-15C) produced from China anthracite.

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Mg-Al 복합 황산염 수화물의 열분해 속도 (Kinetics of the Thermal Decomposition of Mg-Al Sulfate Hydrate)

  • 박홍채;오기동
    • 한국세라믹학회지
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    • 제24권5호
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    • pp.417-422
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    • 1987
  • Kinetic studies were made on the thermal decomposition of hydrated magnesium aluminum double sulfate by a nonisothermal TG method. Thermal analyses of the dehydration of tricosahydrate showed that the reaction proceeded via decahydrate to the anhydrous MgAl2(SO4)4 in the range 50$^{\circ}$to 400$^{\circ}C$. Decomposition of MgAl2(SO4)4 occurred as the two-step between 650$^{\circ}$ and 970$^{\circ}C$. Dehydration of MgAl2(SO4)4$.$23H2O and a 2D diffusion controlled with an activation energy of 16.6kcal/mole, respectively. MgAl2(SO4)4 fitted the contracting volume model with an activation energy of 10.5kcal/mole, and MgSO4 fitted a contracting area model with an activation of 4.5kcal/mole.

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화학적 활성화에 따른 Ni 담지된 흑연나노섬유의 전기화학적 거동 (Effect of Chemical Activation on Electrochemical behaviors of Ni-loaded Graphite Nanofibers)

  • 유혜민;박수진
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2011년도 춘계학술대회 초록집
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    • pp.159.2-159.2
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    • 2011
  • In this study, we prepared the activated graphite nanofibers (A-GNFs) via chemical activation with KOH reagent. The effect of A-GNFs on the surface and textural properties of Ni-loaded graphite nanofibers (Ni/GNFs) was investigated by X-ray diffraction (XRD), transmission electron microscope (TEM), and Brunauer-Emmett-Teller (BET). The textural properties of samples were investigated by $N_2$/77K adsorption isotherms. The electrochemical performances were investigated by cyclic voltammetry. As a results, the electrochemical performances of Ni/GNFs were improved with usage of A-GNFs. This could be interpreted by the high specific surface area and large total pore volume of the A-GNFs.

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Preparation and Characterization of Activated Henequen Fiber

  • Jeong, Jong-Seon;Lee, Young-Seak;Yang, Xiao Ping;Ryu, Seung-Kon
    • Carbon letters
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    • 제10권4호
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    • pp.339-344
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    • 2009
  • Henequen fiber was air-stabilized, carbonized, and steam-activated to obtain high surface area activated henequen fiber (AHF). Thermal behavior of henequen fibers has been studied by TGA. The structural morphology and characteristics were observed by SEM and BET surface area measurement. The yield of AHF from natural henequen was in the range of 20~25 wt%. Mesopores (2~2.5 nm) were developed on the AHF as the activation temperature was raised up to $700^{\circ}C$, and the band of mesopore size distribution moved to 15~30 nm when the activation were carried out at $900^{\circ}C$ for 30 min. The specific surface area and the total pore volume were about $1394\;m^2/g$ and $1.30\;cm^3/g$, respectively at this activation conditions.

The investigation of Magnetohydrodynamic nanofluid flow with Arrhenius energy activation

  • Sharif, Humaira;Khadimallah, Mohamed A.;Naeem, Muhammad Nawaz;Hussain, Muzamal;Mahmoud, S.R.;Al-Basyouni, K.S.;Tounsi, Abdelouahed
    • Advances in nano research
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    • 제10권5호
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    • pp.437-448
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    • 2021
  • In this article, an analytically and numerically 3D nanoliquid flow by a porous rotatable disk is presented in the presence of gyrotactic microorganisms. The mathematical model in the form of partial differential system is transmuted into dimensionless form by utilizing the appropriate transformation. The homotopy analysis approach is applied to attain the analytic solution of the problem. The effect of promising parameters on velocity distribution, temperature profile, nanoparticles volume fraction and motile microorganism distribution field are evaluated through graphs and in tabular form. The existence of Brownian motion and thermophoresis impacts are more proficient for heat transfer enhancement. Further the unique features like heat absorption/generation and energy activation are also examined for the present flow problem. The obtained results are compared with the earliear investigation to check the accuracy of present model.

Chemical Activation Characteristics of Pitch-Based Carbon Fibers by KOH

  • Jang, Jeen-Seok;Lee, Young-Seak;Kim, In-Ki;Yim, Going
    • Carbon letters
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    • 제1권2호
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    • pp.69-75
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    • 2000
  • Naphtha cracking bottom oil was reformed with heat treatment and then spun at $310^{\circ}C$. These pitch-based carbon fibers were carbonized at $1000^{\circ}C$ after oxidation at $280^{\circ}C$, for 90 min. These fibers were chemically activated with molar ratio of KOH/CF (1 : 1) at different temperatures ($250{\sim}900^{\circ}C$) for 1 hr. The process of activation was characterized with DTA, TGA, BET surface area and pore size distribution. The activation of fibers by KOH was performed by several process. One is the reduction process that carbon fiber was reacted with $K_2O$ produced from dehydration process above $400^{\circ}C$. The other is the process that $K_2CO_3$ was directly reacted with carbon fiber. At $800^{\circ}C$, the activation was performed by catalyzed mechanism that $K_2O$ was obtained from the reaction of metal potassium with $CO_2$, then was changed to $K_2CO_3$. At $870^{\circ}C$, the activation was also observed that activation mechanism was promoted by metal catalyst with $CO_2$ from decomposition of $K_2CO_3$. The specific surface area of prepared activated carbon fibers was dependent on the activation mechanism. The specific surface area was in the range of $1519{\sim}2000\;cm^3/g$ and was the largest prepared at $870^{\circ}C$. The pores developed were mostly micropores which was very narrow and uniform. The total pore volume was $0.58{\sim}0.77\;cm^3/g$.

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함산소불소화 효과에 의한 전기방사 활성탄소나노섬유의 $CO_2$ 저장 (Effect of oxyfluorination on activated electrospun carbon nanofibers for $CO_2$ storage)

  • 배병철;김종구;임지선;이영석
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2011년도 춘계학술대회 초록집
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    • pp.219.2-219.2
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    • 2011
  • The oxyfluorination effects of electrospun carbon nanofibers (OFACFs) were investigated for $CO_2$ storage. Carbon nanofibers were prepared form poly acrylonitrile / N,N-dimethylformamide solution through electrospinning method and heat treatment. Chemical activation of carbon nanofibers were carried out in order to improve the pore structure. And the surface modification of activated carbon nanofibers was conducted by oxyfluorination to improve the $CO_2$ storage on effect of introduced functional groups. The samples were labeled CF (electrospun carbon nanofiber), ACF (activated carbon nanofibers), OFACF-1 ($F_2:O_2$ = 3:7), OFACF-2 ($F_2:O_2$ = 5:5) and OFACF-3 ($F_2:O_2$ = 7:3). The functional group of OFACFs was investigated by x-ray photoelectron spectroscopy analysis. The specific surface area, pore volume and pore size of OFACFs were calculated and pore shape was estimated by the BET equation. Through the adsorption isotherm, the specific surface area and pore volume significantly decreased by oxyfluorination.

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1-Heptene, 2-Heptene 및 3-Heptene의 발화특성에 관한 연구 (A Study on Autoignition Characteristics of 1-Heptene, 2-Heptene and 3-Heptene.)

  • 최재욱;목연수;김상렬
    • 한국안전학회지
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    • 제5권2호
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    • pp.17-23
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    • 1990
  • This study was performed by experiments with ASTM's apparatus for determination of autoignition temperature to obtain autoignition characteristics of 1-Heptene, 2-Heptene and 3-Heptene, respectively. As results, minimum autoignition temperatures (MAIT) of 1-Heptene, 2-Heptene and 3-Heptene were 246$^{\circ}C$, 248$^{\circ}C$ and 254$^{\circ}C$, respectively and each dropping volume of these temperatures was 0.25$m\ell$, 0.20$m\ell$ and 0.20$m\ell$. Instantaneous ignition temperatures measured at each dropping volume of Heptene were 371$^{\circ}C$, 357$^{\circ}C$ and 342$^{\circ}C$, respectively. Relation ignition delay time with ignition temperature at minimum autoignition temperature agreed well with Semenov's equation, and the values of apparent activation energy from this equation were 47Kca1/mo1 for 1-Heptene, 35Kca1/mo1 for 2-Heptene and 29Kca1/mo1 for 3-Heptene. It was found that the values of apparent activation energy decreased as the position of double bond changed from end to center in C-C chain.

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저농도 이산화탄소 포집용 활성탄소섬유 흡착제의 질소작용기 함침연구 (Impregnation of Nitrogen Functionalities on Activated Carbon Fiber Adsorbents for Low-level CO2 Capture)

  • 황수현;김동우;정동원;조영민
    • 한국대기환경학회지
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    • 제32권2호
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    • pp.176-183
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    • 2016
  • Activated carbon fibers (ACFs) for $CO_2$ adsorption were prepared from polyacrylonitrile (PAN) fiber through the systematic processes such as oxidation, activation and amination with the focus on the formation of nitration functional groups. Textural analysis of test samples revealed the decrease of specific surface area and pore volume by chemical activation including amination. The ratio of micropores to the total volume was 0.85 to 0.91, which was high enough with the pore size of 1.57 to 1.77 nm. Nitrogen compounds such as imine, pyridine and pyrrole presenting favorable interforces to $CO_2$ molecules were formed throughout the whole preparation steps. The aminated ACF adsorbent showed the enhanced adsorption capacity, 0.40 mmol/g for low-level $CO_2$ flow (3000 ppm) at room temperature. Selectivity of $CO_2$ against dry air ($O_2$ & $N_2$) also increased from 1.00 to 4.66 by amination.