• 제목/요약/키워드: Carbon oxidation

검색결과 1,102건 처리시간 0.023초

Improvement of Oxidation Resistance by Coating on C/BN Composites

  • Kim, Dong-Pyo;Park, Hee-Dong;Lee, Jae-Do
    • The Korean Journal of Ceramics
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    • 제1권3호
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    • pp.155-159
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    • 1995
  • Borosilicate, $B_2O_3$ and BN derived from liquid precursors have been tested as shielding materials for the long period of oxidation resistance of C/BN composites at $650^{\circ}C$. Borosilicate coating displayed excellent oxidation resistance and low moisture absorbance, while $B_2O_3$ and BN were less effective in elevating the oxidation resistance. The enhancement of the oxidation resistance was explained as self-healing effect by viscous flow of the borosilicate glass over Tg, resulting in the reduction of the exposed carbon fibers in a BN matrix.

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리싸이클 CFRP 적용 C/C 복합재료 제조 및 특성 연구 (Study of Manufacturing Process and Properties of C/C Composites with Recycled Carbon Fiber Reinforced Plastics)

  • 김세영;한인섭;방형준;김수현;성영훈;이슬희
    • Composites Research
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    • 제35권4호
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    • pp.242-247
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    • 2022
  • 본 연구는 기존의 폐CFRP를 재활용하여 얻은 재생 탄소섬유를 다시 CFRP 제조에 활용하는 대신 탄소를 모재로 구성하는 탄소/탄소 (Carbon/Carbon, C/C) 복합소재를 제조하는 원료로 활용하기 위한 것이다. 먼저 일반적으로 많이 활용되는 에폭시수지 복합재료의 열분해 공정에 산화-불활성 분위기 변환 기술을 적용하여 1~2% 수준의 잔탄률을 19%까지 향상시켰으며, 이를 통해 에폭시수지 활용 C/C 복합재료 제조 가능성을 확인하였다. 다만, 산화-불활성 분위기 제어를 통한 열분해 공정으로 얻은 탄소의 경우 산소결합도가 높아 추후 개선 연구가 필요한 것으로 나타났다. 또한, 폐CFRP를 열분해 열처리 후 파쇄 및 해쇄 공정을 통해 단섬유 C/C 복합재료 시험편을 제조하였으며 이에 대한 기계적 물성 평가를 통해 최적 공정 조건을 도출하였다.

Effect of H2O2 modification of H3PW12O40@carbon for m-xylene oxidation to isophthalic acid

  • Fang, Zhou-wen;Wen, Di;Wang, Zhi-hao;Long, Xiang-li
    • Korean Journal of Chemical Engineering
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    • 제35권11호
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    • pp.2172-2184
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    • 2018
  • The production of isophthalic acid (IPA) from the oxidation of m-xylene (MX) by air is catalyzed by $H_3PW_{12}O_{40}$ (HPW) loaded on carbon and cobalt. We used $H_2O_2$ solution to oxidize the carbon to improve the catalytic activity of HPW@C catalyst. Experiments reveal that the best carbon sample is obtained by calcining the carbon at $700^{\circ}C$ for 4 h after being impregnated in the 3.75% $H_2O_2$ solution at $40^{\circ}C$ for 7 h. The surface characterization displays that the $H_2O_2$ modification leads to an increase in the acidic groups and a reduction in the basic groups on the carbon surface. The catalytic capability of the HPW@C catalyst depends on its surface chemical characteristics and physical property. The acidic groups play a more important part than the physical property. The MX conversion after 180 min reaction acquired by the HPW@C catalysts prepared from the activated carbon modified in the best condition is 3.81% over that obtained by the HPW@C catalysts prepared from the original carbon. The IPA produced by the former is 46.2% over that produced by the latter.

Oxidation of Fe-(5.3-29.8)%Mn-(1.1-1.9)%Al-0.45%C Alloys at 550-650 ℃

  • Park, Soon Yong;Xiao, Xiao;Kim, Min Ji;Lee, Geun Taek;Hwang, Dae Ho;Woo, Young Ho;Lee, Dong Bok
    • Corrosion Science and Technology
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    • 제21권1호
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    • pp.53-61
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    • 2022
  • Alloys of Fe-(5.3-29.8)%Mn-(1.1-1.9)%Al-(0.4-0.5)%C were oxidized at 550 ℃ to 650 ℃ for 20 h to understand effects of alloying elements on oxidation. Their oxidation resistance increased with increasing Mn level to a small extent. Their oxidation kinetics changed from parabolic to linear when Mn content was decreased and temperature was increasing. Oxide scales primarily consisted of Fe2O3, Mn2O3, and MnFe2O4 without any protective Al-bearing oxides. During oxidation, Fe, Mn, and a lesser amount of Al diffused outward, while oxygen diffused inward to form internal oxides. Both oxide scales and internal oxides consisted of Fe, Mn, and a small amount of Al. The oxidation of Mn and carbon transformed γ-matrix to α-matrix in the subscale. The oxidation led to the formation of relatively thick oxide scales due to inherently inferior oxidation resistance of alloys and the formation of voids and cracks due to evaporation of manganese, decarburization, and outward diffusion of cations across oxides.

Removal of toxic hydroquinone: Comparative studies on use of iron impregnated granular activated carbon as an adsorbent and catalyst

  • Tyagi, Ankit;Das, Susmita;Srivastava, Vimal Chandra
    • Environmental Engineering Research
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    • 제24권3호
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    • pp.474-483
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    • 2019
  • In this study, iron (Fe) impregnated granular activated carbon (Fe-GAC) has been synthesized and characterized for various properties. Comparative studies have been performed for use of Fe-GAC as an adsorbent as well as a catalyst during catalytic oxidation of hydroquinone (HQ). In the batch adsorption study, effect of process parameter like initial HQ concentration ($C_o=25-1,000mg/L$), pH (2-10), contact time (t: 0-24 h), temperature (T: $15-45^{\circ}C$) and adsorbent dose (w: 5-50 g/L) have been studied. Maximum HQ adsorption efficiency of 75% was obtained at optimum parametric condition of: pH = 4, w = 40 g/L and t = 14 h. Pseudo-second order model best-fitted the HQ adsorption kinetics whereas Langmuir model best-represented the isothermal equilibrium behavior. During oxidation studies, effect of various process parameters like initial HQ concentration ($C_o:20-100mg/L$), pH (4-8), oxidant dose ($C_{H2O2}:0.4-1.6mL/L$) and catalyst dose (m: 0.5-1.5 g/L) have been optimized using Taguchi experimental design matrix. Maximum HQ removal efficiency of 83.56% was obtained at optimum condition of $C_o=100mg/L$, pH = 6, $C_{H2O2}=0.4mL/L,$ and m = 1 g/L. Overall use of Fe-GAC during catalytic oxidation seems to be a better as compared to its use an adsorbent for treatment of HQ bearing wastewater.

한중콘크리트 개선을 위한 철가루와 활성탄 혼입 경화체 기초연구 (Properties of Iron Powder and Activated Carbon mixed Matrix for the Improvement of Cold Weather Concrete)

  • 김원종;김원식;김규용;이상수
    • 한국건축시공학회:학술대회논문집
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    • 한국건축시공학회 2022년도 가을 학술논문 발표대회
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    • pp.175-176
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    • 2022
  • By studying the characteristics of matrix insulated through heat generated through oxidation of iron powder, the basic research results on the possibility of buffering and applicability of Cold weather concrete as a curing method are presented. In order to prevent freezing due to a sharp decrease in temperature in the initial stage of curing, iron powder (Fe), powder activated carbon, which is a small amount of porous carbonaceous adsorbent, and salt (NaCl) as an oxidizing agent are replaced with iron powder admixture. As the curing temperature increases, the strength tends to increase, and when replacing the admixture at the same curing temperature, the strength slightly decreases. This is determined as a result of generating iron oxide through an oxidation reaction of iron powder, activated carbon, and NaCl generating a large amount of pores in the matrix. In addition, the internal temperature tends to increase as the mixing substitution rate increases, and it is judged that the oxidation heat of the iron powder mixture affects the increase of the internal temperature during curing. The higher the replacement rate of the iron powder mixture, the slightly lower the strength, but it is determined that freezing and melting that may occur in the early stage of curing can be prevented due to an increase in the initial internal temperature.

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탄소-탄소 복합재의 내삭마 내산화 코팅을 위한 초고온 세라믹스의 적용 (Application of ultra-high-temperature ceramics to oxidation-resistant and anti-ablation coatings for carbon-carbon composite)

  • 김현미;최성철;조남춘;이형익;최균
    • 한국결정성장학회지
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    • 제29권6호
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    • pp.283-293
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    • 2019
  • 우주공간, 고에너지 플라즈마, 방사선 조사 환경과 같은 극한환경에서의 응용 분야가 증가함에 따라 더 높은 용융점 및 기계적 강도, 열전도도의 향상을 필요로 하는 재료에 대한 수요가 계속적으로 증가하고 있다. 이에 따라 대표적인 내열 소재인 탄소-탄소 복합체의 내산화/내삭마 특성을 개선하기 위하여 초고온 세라믹스를 이용하는 방법에 대하여 리뷰하였다. 초고온 세라믹스를 합성하는 가장 간단한 방법인 CVD 코팅법과 다른 코팅법인 pack cementation, 용사법의 장단점을 서로 비교하였다. 복잡한 형상의 C/C 복합체에 CVD 코팅법을 적용하기 위한 방법으로 열역학 계산 및 CFD 시뮬레이션의 활용 가능성을 제안하였다. 또한 이런 방법을 통하여 제작한 TaC/SiC 이중 층 코팅과 TaC/SiC 다중 층 코팅의 내산화 특성을 비교한 결과, 다중 층 코팅을 적용하였을 때 더 뛰어난 내산화성을 보이는 것을 확인하였다.