• Title/Summary/Keyword: Micropores

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Multi-level Analysis of Prefinitely Strainely concrete materials (대변형률이 발생한 콘크리트 재료의 다수준 해석)

  • 최재혁;송하원;김장호;박상순;변근주
    • Proceedings of the Korea Concrete Institute Conference
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    • 2000.04a
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    • pp.405-410
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    • 2000
  • Multi-level (macro-level, meso-level, and micro-level) mechanism of prefinitely strained concrete materials os studied The multi-level analysis explains the additional quasibrittle concrete material ductility that comes from lateral confinement and their multi-level interaction mechanisms. The so-called "upgraded tube-squash test" is used to achieve 50% axial strain and over 70 degree of deviatoric strain of quasibrittle concrete materials under extremely high pressure without producing visible cracks. In the micro-level analysis, the variations of hydration rte, micropores, and hydrate phased are analyzed. In the meso-level analysis, mesocracks (the initial invisible cracks) at the interfaces between aggregates and cement paste matrices are studied. The high confining effect in the specimen on the meso-level cracks is also studied. In the macro-level analysis, the physical behavior of prefinitely strained concrete materials is studied. The co-relationships of the results from the three distinct levels of analyses based in various prestraining (0%, 15%, 35%, and 50%) are studied. For the extremely deformed or strained concrete problems, multi-level analysis will be used to explain the unclear and unstudied mechanism of concrete materials, The multi-level analysis can provide us with valuable insights that can explain the additional ductility and confining effect in concrete. concrete.

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Comparative studies of porous carbon nanofibers by various activation methods

  • Lee, Hye-Min;Kang, Hyo-Rang;An, Kay-Hyeok;Kim, Hong-Gun;Kim, Byung-Joo
    • Carbon letters
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    • v.14 no.3
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    • pp.180-185
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    • 2013
  • In this study, activated carbons nanofibers (ACNFs) were prepared from polyacrylonitrile-based nanofibers by physical ($H_2O$ and $CO_2$) and chemical (KOH) activation. The surface and structural characteristics of the porous carbon were observed by scanning electron microscopy and X-ray diffraction, respectively. Pore characteristics were investigated by $N_2$/77K adsorption isotherms. The specific surface area of the physically ACNFs was increased up to $2400m^2/g$ and the ACNFs were found to be mainly composed of micropore structures. Chemical activation using KOH produced ACNFs with high specific surface area (up to $2500m^2/g$), and the micropores were mainly found in the ACNFs. The physically and chemically ACNFs showed both mainly type I from the International Union of Pure and Applied Chemistry classification.

Partial Discharge Characteristics in LLDPE-Natural Rubber Blends: Correlating Electrical Quantities with Surface Degradation

  • Aulia, Aulia;Ahmad, Mohd Hafizi;Abdul-Malek, Zulkurnain;Arief, Yanuar Z.;Lau, KwanYiew;Novizon, Novizon
    • Journal of Electrical Engineering and Technology
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    • v.11 no.3
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    • pp.699-706
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    • 2016
  • Partial discharges (PD) lead to the degradation of high voltage cables and accessories. PD activities occur due to the existence of impurities, voids, contaminants, defects and protrusions during the manufacture and installation of power cables. Commonly, insulation failures occur at cable joints and terminations, caused by inhomogeneous electric field distributions. In this work, a blend of natural rubber (NR) and linear low density polyethylene (LLDPE) was investigated, and the optimal formulation of the blend that could resist PD was discussed. The experiments were conducted under a constant high voltage stress test of 6.5 kV AC and the magnitude of partial discharge activities was recorded using the CIGRE method II. Pattern analysis of PD signals was performed along with the interpretation of morphological changes. The results showed that the addition of 10 wt% of NR and 5 wt% of Alumina Trihydrate (ATH) provided promising results in resisting PD activities. However, as the NR content increased, more micropores existed, thus resulting in increased PD activities within the samples.

Preparation of Activated Carbon Fiber Adsorbent for Enhancement of CO2 Capture Capacity (이산화탄소 포집능 향상을 위한 활성탄소 섬유 흡착제 제조)

  • Hwang, Su-Hyun;Park, Hyun-Soo;Kim, Dong-woo;Jo, Young-Min
    • Journal of Korean Society for Atmospheric Environment
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    • v.31 no.6
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    • pp.538-547
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    • 2015
  • Test activated carbon fiber (ACF) was prepared from Polyacrylonirile (PAN) through oxidation and chemical activation. Immersion of ACF precursors in the aqueous KOH solution enhanced the surface structure, as examined by BET pore analysis. Specific surface area increased greatly from less than $70m^2/g$ to $1226m^2/g$ with 4 M KOH, and total pore volume also rose up to $0.483cm^3/g$. In particular, it was found that micropores favorable for $CO_2$ molecule capture occupied more than 95%. Maximum $CO_2$ adsorption capacity was 3.59 mmol/g at 298 K. Low depth of pores in the present ACF may facilitate the molecules' desorption for its regeneration.

Adsorption and Antibacterial Properties of Metal Ion Treated Activated Carbon Fiber (금속이온이 처리된 활성탄소섬유의 흡착과 항균성)

  • Oh, Won-Chun;Bang, Seong-Ho
    • Analytical Science and Technology
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    • v.13 no.2
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    • pp.131-135
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    • 2000
  • We studied adsorption isotherm, surface properties and antibacterial activity of Cu treated activated carbon fiber (ACF). The BET surface area of Cu treated ACF are distributed to $688.2-887.8m^2/g$. The adsorption results show that BET surface areas move gradually to lower value with increasing treated Cu mole concentration. Using t-method, the specific micropore volumes and average pore size were obtained. From the SEM study, it is also observed that many of micropores in activated carbon fiber are blocked surface after the treatment. And we also observed that the activity of E. coli in kind of colon bacillus increases gradually to larger range with increasing Cu mole ratio. From these results, we suggest the antibacterial mechanism for metal treated ACF.

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Adsorption Behavior of Primary amine on Activated carbon Rayon-fiber Surfaces as Induced by Oxygen Functional Complexes (Rayon계 ACF의 표면 산소관능기 도입과 Primary amine의 흡착 거동)

  • Kim, Byeoung-Ku;Shin, Hae-Geun;Seo, Jung-Kyu;Lee, Moon-Young;Ji, Sang-Un
    • Journal of the Korean Society of Tobacco Science
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    • v.31 no.1
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    • pp.9-17
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    • 2009
  • Activated carbon fiber (ACF) was surface modified by nitric acid to improve the adsorption efficiency of the propylamine. Functional groups and textural properties of modified ACF were investigated. The total surface acidity increased about 7 times to that of as-received ACF by modification with 1 M nitric acid solution, carboxylic and phenolic groups mainly increased. However, the specific surface areas and the total pore volumes of the modified ACFs were decreased by 5-8% due to the increased blocking (or demolition) of micropores in the presence of newly introduced complexes. Despite the decrease of textural properties, it was found that the amount of propylamine adsorbed by the modified ACFs was increased by approximately 17%. The oxygen and nitrogen contents on the modified ACF increased by 1.5 and 3 times compared with the as-received ACF. From the XPS results, it was observed that propylamine reacted with strong or weak acidic groups, such as -COOH or -OH on the ACF surfaces, resulting in the formation of pyrrolic-, pyridonic- or pyridine-like structures.

Effect of Fe Contents in Fe-AC/Tio2 Composites on Photodegradation Behaviors of Methylene Blue

  • Oh, Won-Chun;Chen, Ming-Liang;Zhang, Feng-Jun;Jang, Hyun-Tae
    • Journal of the Korean Ceramic Society
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    • v.45 no.6
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    • pp.324-330
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    • 2008
  • Activated carbon/$TiO_2$ (AC/$TiO_2$) composites modified with different concentrations of Fe were prepared. The $N_2$ adsorption data showed that the composites had decreased surface area compared with the pristine activated carbon. This indicated the blocking of the micropores on the surface of AC, which was further supported by observation via SEM. XRD results showed patterns for the composites and an anatase typed titanium dioxide structure with a small part of rutile in a higher Fe concentration (> 1.0 mol/L). EDX results showed the presence of C and, O, with Ti peaks on the composites of Fe-AC/$TiO_2$ with relatively lower Ti concentration, which may be due to the higher Fe concentration incorporated into the composites. Subsequently, the photocatalytic effects on methylene blue (MB) were investigated. The improved decomposition of MB showed the combined effects of adsorptions and photodegradation. Especially, the composites modified by Fe revealed enhanced photodegradation behaviors of MB.

Activated Carbon Fibers from Chemically Modified Coal Tar Pitches

  • Ryu, S.K.;Shim, J.W.;Yang, K.S.;Mochida, I.
    • Carbon letters
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    • v.1 no.1
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    • pp.6-11
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    • 2000
  • Coal tar pitch was chemically modified with 10 wt% benzoquinone (BQ) to raise the softening point of isotropic pitch precursor and the precursor was melt-spun into pitch fibers, stabilized, carbonized and activated with steam at $900^{\circ}C$. The weight loss of carbon fiber-benzoquinone (CF-BQ) increased with the increase of activation time like other fibers, but was lower than those of Kureha fiber at the same activation time in spite of larger geometric surface area. Those adsorption isotherms fitted into 'Type I' according to Brunauer, Deming, Deming and Teller classification. However, there was very thin low-pressure hysteresis that lower closure points of the hysteresis are about 0.42-0.45. From the pore size distribution curves, there might be some micropores having narrow-necked bottle; a series of interconnected pore is more likely than discrete bottles. FT-IR studies showed that the functional groups such as carboxyl, quinone, and phenol were introduced to ACFs-BQ surface after steam activation. Methylene blue decolorization and iodine adsorption capacity of ACF-BQ increased linearly with the increase of specific surface area and was larger than that of ACF-Kureha at the same specific surface area.

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Patterned Surfaces in Self-Organized Block Copolymer Films with Hexagonally Ordered Microporous Structures

  • Hayakawa Teruaki;Kouketsu Takayuki;Kakimoto Masa-alki;Yokoyama Hideaki;Horiuchi Shin
    • Macromolecular Research
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    • v.14 no.1
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    • pp.52-58
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    • 2006
  • A novel fabrication of the patterned surfaces in the polymer films was demonstrated by using the self-organizing character of the block copolymers of polystyrene-b-oligothiophenes and polystyrene-b-aromatic amide dendron. Hexagonally arranged open pores with a micrometer-size were spontaneously formed by casting the polymer solutions under a moist air flow. The amphiphilic character of the block copolymers played the crucial role as a surfactant to stabilize the inverse emulsion of water in the organic solvent, and subsequently the aggregated structure of the hydrophilic oligothiophene or aromatic amide dendron segments remained on the interiors of the micropores. The chemical composition on the top of the surface of the microporous films was characterized by energy-filtering transmission electron microscopy (EFTEM) or a time-of-flight secondary ion mass spectrometer (ToF-SIMS). The characterizations clearly indicated that the patterned surfaces in the self-organized block copolymer films with the hexagonally ordered microporous structures were fabricated in a single step.

Investigation of Narrow Pore Size Distribution on Carbon Dioxide Capture of Nanoporous Carbons

  • Meng, Long-Yue;Park, Soo-Jin
    • Bulletin of the Korean Chemical Society
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    • v.33 no.11
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    • pp.3749-3754
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    • 2012
  • Nanoporous carbons with a high specific surface area were prepared directly from thermoplastic acrylic resin as carbon precursor and MgO powder as template by carbonization over the temperature range, $500-1000^{\circ}C$. The effect of the carbonization temperature on the pore structure and $CO_2$ adsorption capacity of the obtained porous carbon was examined. The textural properties and morphology of the porous carbon materials were analyzed by $N_2/-196^{\circ}C$ and $CO_2/0^{\circ}C$ adsorption/desorption isotherms, SEM and TEM. The $CO_2$ adsorption capacity of the prepared porous carbon was measured at $25^{\circ}C$ and 1 bar and 30 bar. The specific surface area increased from 237 to $1251m^2/g$, and the total pore volumes increased from 0.242 to $0.763cm^3/g$ with increasing the carbonization temperature. The carbonization temperature acts mainly by generating large narrow micropores and mesopores with an average pore size dependent on the level of carbonization of the MgO-templated nanoporous carbons. The results showed that the MgO-templated nanoporous carbons at $900^{\circ}C$ exhibited the best $CO_2$ adsorption value of 194 mg/g at 1 bar.