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Effect of gold addition by the recharge method on silver supported catalysts in the catalytic wet air oxidation (CWAO) of phenol

机译:苯酚催化湿空气氧化(Cwao)中银负载催化剂对金加入的影响

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摘要

Catalysts Ag/ZrO2-CeO2 and Au/ZrO2-CeO2 were synthesized by a deposition-precipitation method and Ag-Au/ZrO2-CeO2 was prepared using a recharge method for the second metal (Au). The materials were characterized by physisorption of N-2, XRD, ICP, UV-vis RDS, H2-TPR, XPS and TEM. The results obtained show that the specific areas for monometallic materials were 29-37 m(2) g(-1) and 27-74 m(2) g(-1) for bimetallics. The tetragonal crystal phase of ZrO2 stabilizes when CeO2 quantity increases. Using XPS an increment in Ce3+ species abundance was determined for bimetallic catalysts in contrast to the monometallic ones; according to the Ag 3d region, this metal oxidation was observed when augmenting the content of CeO2 in the materials, and with Au the opposite effect was produced. It was determined by TEM, that the average size of the metallic particles was smaller at bimetallic catalysts due the preparation method. Catalytic activity was evaluated by CWAO of phenol, the Ag-Au/ZrO2-CeO2 catalyst with 20% wt of cerium reached a degradation of 100% within an hour, being the most active catalyst. Maleic, formic and oxalic acid were identified as reaction intermediates; and at the end of the reaction acetic acid was identified as the main by-product, because it is the most refractory and the conditions for oxidation must be more severe.
机译:通过沉淀沉淀法合成催化剂Ag / ZrO2-CeO 2和Au / ZrO2-CeO 2,使用用于第二金属(Au)的再充电方法制备Ag-Au / ZrO2-CeO 2。通过N-2,XRD,ICP,UV-VIS RDS,H2-TPR,XPS和TEM的理由表征所述材料。得到的结果表明,对于二微金属,单金属材料的特定区域为29-37m(2)克(-1)和27-74m(2)g(-1)。当CEO2量增加时,ZrO2的四方结晶相稳定。使用XPS在CE3 +物种中的增量与单金属催化剂相比,测定与单金属催化剂相比过敏的催化剂;根据Ag 3D区域,在增强材料中CeO 2的含量和Au产生相反的效果时,观察到这种金属氧化。它由TEM确定,由于制备方法,金属颗粒的平均尺寸较小。苯酚的Cwao评估催化活性,具有20%wt的Ag-Au / ZrO2-CeO2催化剂在一个小时内达到100%的降解,是最活性的催化剂。将马来酸,甲状腺和草酸被鉴定为反应中间体;并且在反应结束时鉴定乙酸作为主要副产物,因为它是最难治性的,氧化条件必须更严重。

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  • 来源
    《RSC Advances》 |2019年第20期|共12页
  • 作者单位

    Univ Juarez Autonoma Tabasco Lab Nanomat Catalit Aplicados Desarrollo Fuentes CICTAT DACB Km 1 Carretera Cunduacan Jalpa de Mendez Ap 24 Cunduacan 86690 Tabasco Mexico;

    Univ Juarez Autonoma Tabasco Lab Nanomat Catalit Aplicados Desarrollo Fuentes CICTAT DACB Km 1 Carretera Cunduacan Jalpa de Mendez Ap 24 Cunduacan 86690 Tabasco Mexico;

    Univ Juarez Autonoma Tabasco Lab Nanomat Catalit Aplicados Desarrollo Fuentes CICTAT DACB Km 1 Carretera Cunduacan Jalpa de Mendez Ap 24 Cunduacan 86690 Tabasco Mexico;

    Univ Juarez Autonoma Tabasco Lab Nanomat Catalit Aplicados Desarrollo Fuentes CICTAT DACB Km 1 Carretera Cunduacan Jalpa de Mendez Ap 24 Cunduacan 86690 Tabasco Mexico;

    Univ Juarez Autonoma Tabasco Lab Nanomat Catalit Aplicados Desarrollo Fuentes CICTAT DACB Km 1 Carretera Cunduacan Jalpa de Mendez Ap 24 Cunduacan 86690 Tabasco Mexico;

    Univ Juarez Autonoma Tabasco Lab Nanomat Catalit Aplicados Desarrollo Fuentes CICTAT DACB Km 1 Carretera Cunduacan Jalpa de Mendez Ap 24 Cunduacan 86690 Tabasco Mexico;

    Univ Juarez Autonoma Tabasco Lab Nanomat Catalit Aplicados Desarrollo Fuentes CICTAT DACB Km 1 Carretera Cunduacan Jalpa de Mendez Ap 24 Cunduacan 86690 Tabasco Mexico;

    Univ Queensland ARC Ctr Excellence Funct Nanomat AIBN St Lucia Qld 4072 Australia;

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  • 正文语种 eng
  • 中图分类 化学;
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