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  • 7/29/2019 1-s2.0-S0008622312010214-main

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    aCollege of Materials Science and Engineering, Taiyuan University of

    Technology, Taiyuan 030024, ChinabSecond Hospital of Shanxi Medical University, Taiyuan 030001, ChinacGeneral Hospital of Yangquan Coal Industry Group Co., Ltd, Yangquan

    045000, ChinadShanxi Academy of medical Sciences, Shanxi Da Yi Hospital, Taiyuan

    030032, China

    Diethylenetriaminepentaacetic acid-functionalized multi-wall

    carbon nanotubes (MWCNT-DTPA) were labeled by 99mTc and

    intravenously administered to rabbits, the radioactivity in differ-

    ent organs was scanned by single photon emission computed

    tomography and a well-type c counter. Results showed that the

    administered MWCNT-DTPA-99mTc was mainly distributed in

    heart, liver, spleen and kidney. Centrifugate from urine was sub-

    jected to transmission electron microscopy analysis which

    showed that MWCNTs could be excreted through the urinary

    system.

    [New Carbon Materials 2012, 27(6): 421426]

    Synergetic effect of conductive additives on the performance of

    high power lithium ion batteries

    Qi Wanga,b, Fang-yuan Suc, Zhi-yuan Tanga, Guo-wei Linga,

    Quan-hong Yanga,c

    aSchool of Chemical Engineering and Technology, Tianjin University,

    Tianjin 300072, ChinabEighteen Research Institute of China Electronics Technology Group

    Corporation, Tianjin 300381, ChinacEngineering Laboratory for Functionalized Carbon Materials, Graduate

    School at Shenzhen, Tsinghua University, Shenzhen 518055, China

    Two commercial conductive additives, carbon black (super P,

    SP) and vapor grown carbon fibers (VGCFs), were used to con-

    struct an effective conducting network in the cathode of commer-

    cial LiFePO4 lithium ion batteries (LIBs). Results suggest that the

    LIB with SP possesses a higher discharge capacity than that with

    VGCFs with the same mass fraction of the additives. The high-

    rate capacity of LIB with SP is much higher than that with VGCFs.

    Furthermore, the LIB with a mixture of these two additives has an

    apparently improved performance in low and high rate discharge

    capacity compared with the LIBs with a single component addi-

    tive with the same mass fraction due to the synergetic effect.

    The same conclusion can be reached for the larger-capacity bat-

    teries (10 Ah or 50 Ah packs). Therefore, the use of two different

    fillers is important for the high power LIBs used in the electric

    vehicle and mass energy-storage industry.

    [New Carbon Materials 2012, 27(6): 427432]

    Preparation of a direct methanol fuel cell tubular cathode support

    from mesocarbon microbeads and graphite

    Hong-jun Nia, Dong Tangb, Ming-qiang Yina,b, Xing-xing Wanga,

    Ping Liaoa, Ming-yu Huanga, Yu Zhua

    aSchool of Mechanical Engineering, Nantong University, Nantong,

    Jiangsu 226019, China

    b School of Automobile and Traffic Engineering, Jiangsu University,

    Zhenjiang, Jiangsu 212013, China

    A tubular cathode support green body for tubular direct meth-

    anol fuel cell was prepared by a gel casting molding method using

    a mixture of mesocarbon microbeads and natural graphite pow-

    der with a mass ratio of 3:2 as carbon precursor. It was sintered

    at 1000 C for 5 h in a graphite boat covered by graphite powder.

    Subsequently, a tubular cathode and a planar anode were

    obtained by coating the supports with slurry containing a catalyst

    and a Nafion membrane in a PTFE suspension. The catalysts for

    the cathode and anode are Pt/C and PtRu/C, respectively. Results

    show that the surface of the tubular cathode support is smooth

    with no distortion. Both the gas diffusion layer and catalyst layer

    of the cathode show a similar porous structure with most of the

    holes in the sub-micron scale, which is favorable for decreasing

    mass transfer resistance and improving catalytic efficiency. A sin-

    gle cell performance test indicates that the sintered cathode

    bodies from the mixture of mesocarbon microbeads and graphite

    can be used as a special-shaped cathode support.

    [New Carbon Materials 2012, 27(6): 433439]

    Preparation and characterization of activated carbons from spirit

    lees by physical activation

    Qiang Lia,b, Yin Wanga, Jian Yua, Bin Yic, Jun Yangc, Guang-wen

    Xua

    a National Key Laboratory of Multiphase Complex System, Institute of

    Process Engineering, Chinese Academy of Sciences, Beijing 100190,

    Chinab CNOOC New Energy Investment Co., Ltd., Beijing 100016, Chinac Luzhou Laojiao Group, Luzhou, Sichuan 646000, China

    Spirit lees was carbonized and then activated by steam and

    CO2 to prepare activated carbons. The effect of carbonization

    temperature, type and amount of activator, activation tempera-

    ture and time on the pore structure, and the adsorption of meth-

    ylene blue and iodine were investigated. The gas products during

    activation were analyzed online to reveal the activation mecha-

    nism. Results showed that steam activation was rather more

    active than CO2. Regardless of the activation agent, a low carbon-

    ization temperature of 450 C and a medium activation tempera-

    ture of 800 C favored the iodine adsorption. For the methylene

    blue adsorption, the same low carbonization temperature of450 C, however, medium/high activation temperatures (850

    900 C) are favorable. The best activated carbon was prepared

    with a steam activator using a carbonization temperature of

    450 C and an activation temperature of 800 C, which had a sur-

    face area and pore volume of 371.6 m2/g and 0.34 cm3/g, and

    iodine and methylene blue adsorption capacities of 580 mg/g

    and 90 mg/g respectively. O- and H-containing functional groups

    in the carbonized spirit lees reacted with the activation regent

    (steam or CO2) to form the initial pores, then the accessible active

    sites reacted with the activation regent to generate secondary

    pores.

    [New Carbon Materials 2012, 27(6): 440447]

    376 CARBON 55 (2013) 375378