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Heterogeneous selective oxidation catalysts based on coordination polymer MIL-101 and transition metal-substituted polyoxometalates

机译:基于配位聚合物MIL-101和过渡金属取代的多金属氧酸盐的多相选择性氧化催化剂

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Titanium- and cobalt- monosubstituted Keggin heteropolyanions, [PW11CoO39](5-) and [PW11TiO40](5-), were electrostatically bound to the chromium terephthalate polymer matrix MIL-101. The MIL-supported polyoxometalate (POM) catalysts were characterized by elemental analysis, XRD, N-2 adsorption, and FT-IR-spectroscopy. The catalytic performance of both MIL-101 and the novel composite materials M-POM/MIL-101 was assessed in the oxidation of three representative alkenes-alpha-pinene, caryophyllene, and cyclohexene-using molecular oxygen and aqueous hydrogen peroxide as oxidants. Ti-POM/MIL-101 demonstrated fairly good catalytic activity and selectivity in alpha-pinene allylic oxidation and caryophyllene epoxidation with hydrogen peroxide, whereas Co-POM/MIL-101 catalyzed alpha-pinene allylic oxidation by molecular oxygen. Both composite materials are stable to POM leaching, behave as true heterogeneous catalysts, and can be used repeatedly without sustaining a loss of activity and selectivity in oxidations with O-2 and H2O2, provided that rather mild reaction conditions (T < 50 degrees C, [H2O2] < 0.2 M) are used with the latter oxidant. (c) 2008 Elsevier Inc. Alt rights reserved.
机译:钛和钴单取代的Keggin杂聚阴离子[PW11CoO39](5-)和[PW11TiO40](5-)与对苯二甲酸铬聚合物基质MIL-101静电结合。 MIL负载的多金属氧酸盐(POM)催化剂通过元素分析,XRD,N-2吸附和FT-IR光谱进行了表征。 MIL-101和新型复合材料M-POM / MIL-101的催化性能都在使用分子氧和过氧化氢水溶液作为氧化剂对三种代表性烯烃-α-pine烯,石竹烯和环己烯的氧化反应中进行了评估。 Ti-POM / MIL-101在过氧化氢的α-pine烯烯丙基氧化和石竹烯环氧化中表现出相当好的催化活性和选择性,而Co-POM / MIL-101通过分子氧催化α-pine烯烯丙基氧化。两种复合材料均对POM浸出稳定,表现为真正的多相催化剂,并且可以重复使用,而不会因O-2和H2O2氧化而丧失活性和选择性,前提是反应条件温和(T <50摄氏度, [H2O2] <0.2 M)与后一种氧化剂一起使用。 (c)2008 Elsevier Inc.版权所有。

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