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原煤与石油焦共气化反应特性 被引量:11
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作者 纪丽媛 黄胜 +2 位作者 吴诗勇 吴幼青 高晋生 《石油学报(石油加工)》 EI CAS CSCD 北大核心 2014年第3期493-500,共8页
采用固定床反应器,以水蒸气为气化介质,研究了金山石油焦和3种不同煤阶原煤(小龙潭褐煤、神府烟煤、高平无烟煤)的共气化反应特性,考察了不同煤阶原煤对煤-石油焦共气化反应活性和产物气组成的影响,以及含碳物料的气化反应活性与其CO... 采用固定床反应器,以水蒸气为气化介质,研究了金山石油焦和3种不同煤阶原煤(小龙潭褐煤、神府烟煤、高平无烟煤)的共气化反应特性,考察了不同煤阶原煤对煤-石油焦共气化反应活性和产物气组成的影响,以及含碳物料的气化反应活性与其CO2吸附量的关系.结果表明,向石油焦中添加一定量的原煤,可在一定程度上改善石油焦的气化反应活性,提高气体产物中H2含量,如小龙潭褐煤的添加量为40%时,其与石油焦共气化反应活性约为石油焦单独气化时的2~3倍,气体产物中H2含量提高了12%;煤与石油焦共气化的反应活性、气体产物中H2以及合成气(H2 +CO)含量均按小龙潭褐煤、神府烟煤、高平无烟煤的顺序依次降低;由于3种原煤中活性金属组分含量的不同,其对应的CO2吸附量表现出一定差异.此外,含碳物料的气化反应速率与CO2强吸附量呈线性关系,拟合强度范围为0.97~0.99,CO2吸附量可作为表征含碳物料气化反应活性大小的一项指标. 展开更多
关键词 石油焦 共气化 co2化学吸附
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Synthesis and evaluation as CO2 chemisorbent of the Li5(Al1-xFex)O4 solid solution materials:Effect of oxygen addition
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作者 Paulina Olavarría Elizabeth Vera +1 位作者 Enrique J.Lima Heriberto Pfeiffer 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2017年第5期948-955,共8页
Pentalithium aluminate(β-LiAlO) and the corresponding iron-containing solid solution(Li(AlFe)O)were synthetized by solid-state reaction. All the samples were characterized structural and microstructurally by X-ray ... Pentalithium aluminate(β-LiAlO) and the corresponding iron-containing solid solution(Li(AlFe)O)were synthetized by solid-state reaction. All the samples were characterized structural and microstructurally by X-ray diffraction, solid-state nuclear magnetic resonance, scanning electron microscopy, Nadsorption-desorption and temperature-programmed desorption of CO. Results showed that 30 mol% of iron can be incorporated into the β-LiAlOcrystalline structure at aluminum positions. Moreover, iron addition induced morphological and superficial reactivity variations. Li(AlFe)Osamples chemisorbed CObetween 200 and 700 °C, where the superficial chemisorption presented the highest enhancement,in comparison to β-LiAlO. Additionally, Li(AlFe)Osamples sintered at higher temperatures thanβ-LiAlO. Isothermal COchemisorption experiments of β-LiAlOand Li(AlFe)Owere fitted to a first order reaction model, corroborating that iron enhances the COchemisorption, kinetically. When oxygen was added to the gas flow, COchemisorption process was mainly enhanced between 400 and 600 °C for the Li(AlFe)Osample in comparison to β-LiAlO. Hence, Li(AlFe)Osolid solution presented an enhanced COchemisorption process, in the presence and absence of oxygen, in comparison to β-LiAlO. 展开更多
关键词 Lithium aluminate co2 chemisorption Solid solution THERMOGRAVIMETRY
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Structural evolution and reaction mechanism of lithium nickelate(LiNiO_(2))during the carbonation reaction
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作者 Daniela Gonzalez-Varela Brenda Alcantar-Vazquez Heriberto Pfeiffer 《Journal of Materiomics》 SCIE EI 2018年第1期56-61,共6页
Lithium nickelate(LiNiO_(2))was synthesized using the lithium excess method,and then characterized by X-ray diffraction,scanning electron microscopy and N_(2) adsorption-desorption.Finally,differential thermal and the... Lithium nickelate(LiNiO_(2))was synthesized using the lithium excess method,and then characterized by X-ray diffraction,scanning electron microscopy and N_(2) adsorption-desorption.Finally,differential thermal and thermogravimetric analyses were performed in CO_(2)presence,at high temperatures.Results show that LiNiO_(2)is able to react with CO_(2)through a complex structural evolution process,where lithium atoms are released to produce Li_(2)CO_(3),while some nickel atoms are rearranged on different Li_(1-x)Ni_(1+x)O_(2)crystalline phases.LiNiO_(2)-CO_(2)reaction kinetic parameters were determined assuming a first-order reaction,where kinetic constants tended to increase as a function of temperature.However,kinetic constant values did not follow a linear trend.This atypical behavior was attributed to LiNiO_(2)sintering and crystalline evolution performed as a function of temperature. 展开更多
关键词 Lithium nickelate co_(2)chemisorption Lithium diffusion coefficient Phase transition
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