Coordination unsaturated structure of titanium sulfate promoting the carbon chain growth for dimethyl ether oxidation

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Abstract

Polyoxymethylene dimethyl ethers (DMMx, CH3O(CH2O)xCH3, x = 1–8) are appealing oxygenated chemicals with potential applications mainly used as sustainable fuels and solvents. The growth of longer C-O chain for direct oxidation of dimethyl ether (DME) to DMMx is especially important, but the construction of the acid sites with different strengths and matched redox sites faces great difficulties. Herein, the gradient acidity and enhanced oxidizability have been successfully created by regulating coordination structure of titanium sulfate (Ti(SO4)x). The formation of a higher proportion of weak-medium acid sites and appropriate redox sites over a Ti(SO4)x/activated carbon (AC) catalyst with nitrogen treatment significantly promotes the synthesis of larger molecules, with DMM2–3 selectivity up to 42.2%. Combined with the characterizations, designed experiments and theoretical calculations, the configurations of Ti(SO4)x and their local chemical environment are revealed. The different distortions of Ti(SO4)x structure in nitrogen atmosphere result in the various coordination unsaturated Ti atoms located at the center of polyhedral, which is the main reason for the gradient acidity distribution and enhanced oxidative property.

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硫酸钛的配位不饱和结构促进二甲醚氧化的碳链增长
聚氧亚甲基二甲醚(DMMx,CH3O(CH2O)xCH3,x = 1-8)是一种极具吸引力的含氧化学品,主要用作可持续燃料和溶剂。在二甲醚(DME)直接氧化成 DMMx 的过程中,增加较长的 C-O 链尤为重要,但构建不同强度的酸性位点和匹配的氧化还原位点面临很大困难。在这里,通过调节硫酸钛(Ti(SO4)x)的配位结构,成功地创造了梯度酸性并增强了氧化性。在氮处理的 Ti(SO4)x/activated carbon (AC) 催化剂上形成较高比例的弱中酸性位点和适当的氧化还原位点,大大促进了大分子的合成,DMM2-3 的选择性高达 42.2%。结合表征、设计实验和理论计算,揭示了 Ti(SO4)x 的构型及其局部化学环境。在氮气氛中,Ti(SO4)x 结构的不同畸变导致位于多面体中心的各种配位不饱和 Ti 原子,这是造成梯度酸性分布和氧化性增强的主要原因。
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