甲醇间接氧化羰基化制碳酸二甲酯的钼促进钯/镍催化剂

IF 15.7 1区 化学 Q1 CHEMISTRY, APPLIED
Ke Huang , Shicheng Yuan , Rongyan Mei , Ge Yang , Peng Bai , Hailing Guo , Chunzheng Wang , Svetlana Mintova
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引用次数: 0

摘要

我们制备了一种由钯修饰的沸石 Y 催化剂(Pd/NaY)组成的无氯催化剂,并将其用于甲醇间接氧化羰基化制备碳酸二甲酯(DMC)。通过自上而下的方法在 Pd/NaY 中引入钼(Pd-Mo/NaY 催化剂),进一步提高了催化剂的活性和稳定性。与 Pd/NaY 催化剂相比,Pd-Mo/NaY 催化剂表现出更高的稳定性。在 30 小时的催化测试中,Pd-Mo/NaY 的 CO 转化率高达 97%,DMC 选择性高达 80%。此外,在 Pd-Mo/NaY 催化剂中,钼的加入可部分修复硅烷醇,并阻碍钯的聚集。Mo 和 Pd 之间的相互作用增加了活性 Pd2+ 物种的数量,并增强了 Pd-Mo/NaY 催化剂对 CO 反应物的吸附。原位漫反射红外傅立叶变换光谱捕捉到了 COOCH3* 的关键反应中间体。活性 Pd2+ 物种的稳定有助于提高 Pd-Mo/NaY 催化剂在甲醇间接氧化羰基化成 DMC 反应中的催化活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mo-promoted Pd/NaY catalyst for indirect oxidative carbonylation of methanol to dimethyl carbonate

A chlorine-free catalyst consisting of zeolite Y modified with Pd (Pd/NaY) catalyst has been prepared and used in the indirect oxidative carbonylation of methanol to dimethyl carbonate (DMC). The activity and stability of the catalyst were further improved by introducing molybdenum into Pd/NaY using a top-down approach (Pd-Mo/NaY catalyst). The Pd-Mo/NaY catalyst exhibited higher stability compared to the Pd/NaY. A high CO conversion of 97% and DMC selectivity of 80% during a 30-hour catalytic test for the Pd-Mo/NaY were obtained. Furthermore, the incorporation of Mo was found to partially heal the silanols and hinder the aggregation of Pd in the Pd-Mo/NaY catalyst. The interactions between Mo and Pd increased the amount of active Pd2+ species and enhanced the adsorption of CO reactant on the Pd-Mo/NaY catalyst. The key reaction intermediate of COOCH3* was captured by in situ diffuse reflectance infrared Fourier transform spectroscopy. The stabilization of active Pd2+ species contributed to the enhanced catalytic activity of the Pd-Mo/NaY catalyst in the indirect oxidative carbonylation of methanol to DMC reaction.

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来源期刊
Chinese Journal of Catalysis
Chinese Journal of Catalysis 工程技术-工程:化工
CiteScore
25.80
自引率
10.30%
发文量
235
审稿时长
1.2 months
期刊介绍: The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.
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