个人信息Personal Information
教授
博士生导师
硕士生导师
主要任职:校长助理
其他任职:精细化工国家重点实验室副主任,辽宁省低碳资源高值化利用重点实验室主任
性别:男
毕业院校:中科院山西煤化所
学位:博士
所在单位:化工学院
学科:工业催化. 化学工艺. 能源化工
办公地点:大连市凌工路2号大连理工大学西部校区化工楼,邮编:116024
联系方式:0411-84986112
电子邮箱:anhuilu@dlut.edu.cn
磷化铁/石墨烯纳米复合物的制备及其在F-T合成反应中的应用
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发表时间:2013-01-01
发表刊物:化学学报
卷号:71
期号:10
页面范围:1365-1368
ISSN号:0567-7351
摘要:Graphene (G) is a huge open it-electron system with a unique electronic structure, which ignites diverse applications such as electronics, photovoltaics, batteries, supercapacitors and so on. Because of the larger surface area, G can be used as the catalyst or the advantageous carrier for the catalytic active components for hydrogenation, oxidation and carbon-carbon coupling reactions. In the present study, we exploited G as a support for iron phosphide nanoparticles (FeP/G) by calcination the precursor iron phosphate-graphene oxide nanocomposite (FePO/GO) under hydrogen atmosphere. In the same method, we also prepared the control pure iron phosphide (FeP) by H-2 calcination the precursor iron phosphate (FePO). The FePO of FePO/GO existed in the form of porous spherical and the particle size ranges from 100 nm to 300 nm. After transforming into FeP, the average particle size of FeP is about 10 mu while the particles were uniformly dispersed on the G and no obvious aggregation was observed. While, not only the pure FePO but also the pure FeP was powerful aggregation. That meant GO and G could regulate the microstructure and morphology of FePO and FeP, respectively. The as-prepared products were investigated by X-ray diffraction, transmission electron microscopy, field emission environment scanning electron microscopy and XPS spectroscopy. XPS spectra showed that the electron binding energy of Fe in FeP/G increased slightly. The Fischer-Tropsch Synthesis (FTS) reaction has been selected as model reaction for evaluating FeP/G. When the reaction conditions were 15 mg catalyst (reduced in H2 at 623 K for 2 h prior to FTS reaction), 2 MPa syngas (CO : H-2 : Ar=32 : 63 : 5), 5 mL.min(-1), 593 K, the remarkable catalytic discrepancies in FTS activity and product selectivity were observed. The activity toward the conversion of CO on FeP/G was about 70 times that of FeP. The result show that FeP/G catalysts are potential good catalysts for FTS.
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