首页|Al、Ti或Zr改性对包埋式Ni@SiO2催化剂甲烷部分氧化制合成气性能的影响

Al、Ti或Zr改性对包埋式Ni@SiO2催化剂甲烷部分氧化制合成气性能的影响

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包埋式结构催化剂能够有效地阻止活性组分的高温烧结,实现甲烷部分氧化(POM)反应高效制合成气。采用Stöber法制备了包埋式Ni@SiO2催化剂,并引入Al、Ti或Zr对其进行改性制得相应的改性催化剂。采用X射线衍射(XRD)、透射电镜(TEM)和N2吸/脱附等对催化剂的晶相结构、形貌和织构性质等进行了表征,并研究了改性对催化剂在POM反应制合成气(原料气组成:V(CH4)∶V(O2)∶V(N2)为2∶1∶3、流量为60 mL/min、压力为0。1 MPa、空速为7。2 L/(g·h)和反应时间为22 h)中催化性能的影响。结果表明,与Ni@SiO2相比,Ni@Al-SiO2可促进甲烷的活化,其催化性能明显提升,Ni@Ti-SiO2和Ni@Zr-SiO2因活性位点的阻碍而催化性能降低。在700 ℃下,反应稳定后,Ni@SiO2和Ni@Al-SiO2的CH4转化率分别为86%和80%,CO选择性均为90%左右,H2选择性分别为93%和88%。经8 h稳定性测试后,与Ni@SiO2相比,Ni@Ti-SiO2和Ni@Zr-SiO2的CH4转化率、CO选择性和H2选择性均明显降低。活性位点的减少和积炭是导致催化剂失活的主要原因,积炭未造成活性位点的完全覆盖,催化剂仍能保持稳定的POM催化性能。
Effects of Al,Ti or Zr modification on performances of embedded Ni@SiO2 catalysts for partial oxidation of methane to syngas
The embedded catalysts can effectively prevent the sintering behavior,and realize the high activity in partial oxidation of methane(POM)reaction.The embedded Ni@SiO2 catalysts were prepared by Stöber method,and the Al,Ti or Zr were used to modify them.Various characterizations,such as X-ray diffraction(XRD),transmission electron microscope(TEM)and N2 adsorption/desorption,were employed to the characterizations of crystalline phase structures,morphologies and texture parameters of catalysts.The effects of modification of catalysts on the catalytic POM performance were further investigated under the feed gases compositions of V(CH4)∶V(O2)∶V(N2)of 2∶1∶3,gas flow rate of 60 mL/min,pressure of 0.1 MPa,space velocity of 7.2 L/(g·h)and reaction time of 22 h.The results show that compared with Ni@SiO2 catalyst,the Ni@Al-SiO2 catalyst can promote the activation of methane and its catalytic performance is improved.However,the Ni@Ti-SiO2 and Ni@Zr-SiO2 catalysts show the decreased catalytic performances because of the obstruction of active sites.At 700 ℃,the CH4 conversation rates of Ni@Al-SiO2 and Ni@SiO2 are 86%and 80%,the CO selectivities are both about 90%,and the H2 selectivities are 93%and 88%,respectively.However,compared with Ni@SiO2catalyst,the CH4 conversion rates,CO selectivities and H2 selectivities of Ni@Ti-SiO2 and Ni@Zr-SiO2 are significantly reduced.It reveals that the catalyst deactivation can be mainly ascribed to the loss of active sites and carbon deposit.But the active sites are not completely covered by deposited carbon,and the catalyst still maintain robust catalytic POM performance.

Ni@SiO2 catalystsembedded structurecatalyst modificationpartial oxidation of methanecarbon deposit

邵景玲、李杰、费兆阳、李雷

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盐城工学院 化学化工学院,江苏 盐城 224051

南京工业大学材料化学工程国家重点实验室,江苏南京 211816

Ni@SiO2催化剂 包埋式结构 催化剂改性 甲烷部分氧化 积炭

材料化学工程国家重点实验室自主课题

SKL-MCE-22B06

2024

天然气化工—C1化学与化工
西南化工研究设计院有限公司 全国天然气化工与碳一化工信息中心

天然气化工—C1化学与化工

CSTPCD北大核心
影响因子:0.814
ISSN:1001-9219
年,卷(期):2024.49(8)