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Hydroisomerization of n-decane over the Pd/ZSM-22 bifunctional catalysts: The effects of dynamic and static crystallization to the zeolite
Microporous and Mesoporous Materials ( IF 5.2 ) Pub Date : 2018-07-09 , DOI: 10.1016/j.micromeso.2018.07.012
Zhaolu Feng , Wei Wang , Yu Wang , Xuefeng Bai , Xiaofang Su , Lan Yang , Wei Wu

Two series of pure nanosized ZSM-22 zeolites (Z-22 (xD) and Z-22 (xS)) with different SiO2/Al2O3 molar ratios are synthesized with 1,6-diaminohexane (DAH) template by the hydrothermal method under dynamic and static crystallization conditions, respectively. The effects of crystallization conditions on the characteristic properties of ZSM-22 zeolites are investigated by XRD, SEM, HR-TEM, N2 adsorption, 29Si and 27Al MAS NMR, NH3-TPD, Py-IR and H2 chemisorption measurements. The results show that Z-22 (xD) samples reveal smaller crystal size, larger mesoporosity, weaker Brønsted acid strength and lower Brønsted acid density compared with Z-22 (xS) samples. The Pd/Z-22 (xD) and Pd/Z-22 (xS) bifunctional catalysts are prepared by loading 0.5 wt% Pd on the corresponding zeolite samples, respectively, and the catalytic performance over all bifunctional catalysts is tested in the hydroisomerization of n-decane. The catalytic test results indicate that the Pd/Z-22 (xD) catalysts show higher selectivity for both mono-branched and multi-branched iso-decanes than those of Pd/Z-22 (xS) catalysts, because of the smaller crystal size and lower Brønsted acidity. Therefore, the dynamic hydrothermal crystallization is an effective way to synthesize ZSM-22 zeolites with improved catalytic behaviors for the n-alkane hydroisomerization.



中文翻译:

Pd / ZSM-22双功能催化剂上癸烷的加氢异构化:动态和静态结晶对沸石的影响

用1,6-二氨基己烷(DAH)模板合成了具有不同SiO 2 / Al 2 O 3摩尔比的两个系列的纯纳米ZSM-22沸石(Z-22(x D)和Z-22(x S))。分别在动态和静态结晶条件下进行水热法。通过XRD,SEM,HR-TEM,N 2吸附,29 Si和27 Al MAS NMR,NH 3 -TPD,Py-IR和H 2化学吸附测量研究了结晶条件对ZSM-22沸石特征性能的影响。。结果表明Z-22(xD)样品与Z-22(x S)样品相比,具有较小的晶体尺寸,较大的介孔率,较弱的Brønsted酸强度和较低的Brønsted酸密度。Pd / Z-22(x D)和Pd / Z-22(x S)双功能催化剂是通过分别在相应的沸石样品上负载0.5 wt%的Pd制备的,并且在该催化剂中测试了所有双功能催化剂的催化性能。癸烷的加氢异构化。催化测试结果表明,Pd / Z-22(x D)催化剂对单支和多支癸烷的选择性均高于Pd / Z-22(xS)催化剂,因为较小的晶体尺寸和较低的布朗斯台德酸度。因此,动态水热结晶法是合成具有改进的正链烷烃加氢异构化催化行为的ZSM-22沸石的有效方法。

更新日期:2018-07-09
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