首页> 外文期刊>Microporous and mesoporous materials: The offical journal of the International Zeolite Association >Alpha-pinene isomerization over Ti-SBA-15 catalysts obtained by the direct method: The influence of titanium content, temperature, catalyst amount and reaction time
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Alpha-pinene isomerization over Ti-SBA-15 catalysts obtained by the direct method: The influence of titanium content, temperature, catalyst amount and reaction time

机译:通过直接方法获得的Ti-SBA-15催化剂上的α-叉烯异构化:钛含量,温度,催化剂量和反应时间的影响

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This work presents the studies on the isomerization of alpha-pinene in the presence of Ti-SBA-15 catalysts with different titanium contents: 0.75, 0.90, 1.10, and 3.10 wt%, as established by the EDX method, and 0.60, 0.76, 1.08, and 2.53 wt%, as measured by the ICP-AES method. These catalysts were prepared by the hydrothermal method and were characterized by the followed instrumental techniques: XRD, UV-Vis, FT-IR. SEM, ICP-AES, EDX, TEM, and AFM. Additionally, textural parameters were determined by N-2 adsorption/desorption. Preliminary studies showed that the most active catalyst was the material prepared from the crystallization gel with the molar ratio of Si:Ti = 20:1. This catalyst was further used for the detailed studies on a-pinene isomerization according to the following parameters: temperature range of 20-200 degrees C, 0.5-20 wt% catalyst content, and reaction times from 15 min to 24 h. The optimal conditions for alpha-pinene isomerization were determined on the basis of its conversion and the selectivity of the produced camphene. This study also showed that the process of alpha-pinene isomerization is complex because subsequent reactions occurred during the process. (C) 2017 Elsevier Inc. All rights reserved.
机译:该工作介绍了在Ti-SBA-15催化剂存在下α-PinENE的异构化的研究:0.75,0.90,1.10和3.10wt%,由EDX方法建立,0.60,0.76, 1.08和2.53wt%,通过ICP-AES方法测量。通过水热法制备这些催化剂,其特征在于效应技术:XRD,UV-Vis,FT-IR。 SEM,ICP-AES,EDX,TEM和AFM。另外,通过N-2吸附/解吸确定纹理参数。初步研究表明,最活性催化剂是由摩尔比的结晶凝胶制备的材料,Si:Ti = 20:1。该催化剂进一步用于根据以下参数对A-Pine烯异构化的详细研究:温度范围为20-200℃,0.5-20重量%的催化剂含量,反应时间为15分钟至24小时。基于其转化率和产生的樟烯的选择性来确定α-突烯异构化的最佳条件。本研究还表明,α-突烯异构化的过程是复杂的,因为在该过程中发生后续反应。 (c)2017年Elsevier Inc.保留所有权利。

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