Defluidization conditions for a fluidized bed of iron oxide-, nickel oxide-, and manganese oxide-containing oxygen carriers for chemical-looping combustion
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Cho, P
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机构:Chalmers Univ Technol, Dept Energy & Environm, S-41296 Gothenburg, Sweden
Cho, P
Mattisson, T
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Chalmers Univ Technol, Dept Energy & Environm, S-41296 Gothenburg, SwedenChalmers Univ Technol, Dept Energy & Environm, S-41296 Gothenburg, Sweden
Mattisson, T
[1
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Lyngfelt, A
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机构:Chalmers Univ Technol, Dept Energy & Environm, S-41296 Gothenburg, Sweden
Lyngfelt, A
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[1] Chalmers Univ Technol, Dept Energy & Environm, S-41296 Gothenburg, Sweden
For combustion with CO2 capture, chemical-looping combustion with inherent separation Of CO2 is a promising technology. Chemical-looping combustion uses oxygen carriers that are composed of metal oxide to transfer oxygen from the combustion air to the fuel. The defluidization of oxygen-carrier particles was investigated to improve the understanding of when particle agglomeration may occur. The study was made in a laboratory fluidized-bed reactor at 950 degrees C, simulating a chemical-looping combustion system by exposing the sample to reducing and oxidizing conditions in an alternating manner. The oxygen-carrier particles used were based on oxides of iron, nickel, and manganese and produced by freeze granulation. For iron oxide particles, there was no defluidization of the bed when the content of available oxygen in the particle was high. The defluidization occurred during the oxidation period after long reduction periods, in which a significant reduction of the magnetite to wustite occurred. This is an important observation, because the reduction to wustite is not expected in chemical-looping combustion with high fuel conversion. Thus, laboratory experiments with iron oxide performed with long reduction times may give an unduly exaggerated impression of the risks of agglomeration. For nickel oxide, the defluidization was dependent on the sintering temperature with no defluidization in experiments conducted with particles sintered at 1300 and 1400 degrees C. The nickel oxide particles that were sintered at 1500 degrees C only defluidized once in a total of 49 cycles, whereas the particles that were sintered at 1600 degrees C defluidized already in the first cycle. For the nickel oxide particles, it was not possible to see any effect of the length of the reducing period on the defluidization. There was no defluidization of the manganese oxide particles. The defluidization of the bed leads to agglomeration for the iron oxide particles, but not for the particles of nickel oxide, where the bed was still loosely packed. Carbon was formed on the particles based on nickel oxide and manganese oxide.
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US DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USAUS DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USA
Siriwardane, Ranjani
Tian, Hanjing
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US DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USA
Parsons, Pittsburgh, PA 15129 USAUS DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USA
Tian, Hanjing
Richards, George
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US DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USAUS DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USA
Richards, George
Simonyi, Thomas
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US DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USA
Parsons, Pittsburgh, PA 15129 USAUS DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USA
Simonyi, Thomas
Poston, James
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US DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USAUS DOE, Natl Energy Technol Lab, Morgantown, WV 26507 USA
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Yeungnam Univ, Dept Chem, Coll Nat Sci, Gyongsan 38541, Gyeongbuk, South KoreaYeungnam Univ, Dept Chem, Coll Nat Sci, Gyongsan 38541, Gyeongbuk, South Korea
Kwak, Byeong Sub
Park, No-Kuk
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Yeungnam Univ, Sch Chem Engn, Gyongsan 38541, Gyeongbuk, South KoreaYeungnam Univ, Dept Chem, Coll Nat Sci, Gyongsan 38541, Gyeongbuk, South Korea
Park, No-Kuk
Ryu, Ho-Jung
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Korea Inst Energy Res, 152 Gajeong Ro, Daejeon 34129, South KoreaYeungnam Univ, Dept Chem, Coll Nat Sci, Gyongsan 38541, Gyeongbuk, South Korea
Ryu, Ho-Jung
Baek, Jeom-In
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Korea Elect Power Corp, Res Inst, 105 Munji Ro, Daejeon 34056, South KoreaYeungnam Univ, Dept Chem, Coll Nat Sci, Gyongsan 38541, Gyeongbuk, South Korea
Baek, Jeom-In
Kang, Misook
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Yeungnam Univ, Dept Chem, Coll Nat Sci, Gyongsan 38541, Gyeongbuk, South KoreaYeungnam Univ, Dept Chem, Coll Nat Sci, Gyongsan 38541, Gyeongbuk, South Korea
机构:
Southeast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R ChinaSoutheast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R China
Shen, Laihong
Wu, Jiahua
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Southeast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R ChinaSoutheast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R China
Wu, Jiahua
Xiao, Jun
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Southeast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R ChinaSoutheast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R China
Xiao, Jun
Song, Qilei
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Southeast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R ChinaSoutheast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R China
Song, Qilei
Xiao, Rui
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Southeast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R ChinaSoutheast Univ, Thermoenergy Engn Res Inst, Nanjing 210096, Peoples R China