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Simple and green route for preparation of tin phosphate catalysts by solid-state grinding for dehydration of glucose to 5-hydroxymethylfurfural (HMF)

机译:通过固态研磨制备磷酸锡催化剂的简单和绿色途径,用于葡萄糖脱水至5-羟甲基糠醛(HMF)

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摘要

This work demonstrated a simple and green method for the synthesis of tin phosphate (SnP) catalysts for glucose to HMF transformation. In this process, SnP catalysts with various P/Sn mole ratios were prepared by solid-state grinding of a mixture of SnCl4 center dot 5H(2)O and NaH2PO4 center dot 2H(2)O at room temperature, followed by drying with or without calcination. Physicochemical properties of the obtained SnP catalysts were investigated using N-2-physisorption, XRD, FT-IR, Py-IR, NH3-TPD, and XPS techniques. The characterization studies showed that varying P/Sn ratio affected the textural and surface acid properties of the SnP catalysts. The activity of these catalysts was evaluated for dehydration of glucose for HMF production in water using recyclable low boiling point organic solvent THF as HMF extracting solvent. The experimental results revealed that the catalytic activity of SnP catalysts depended on the P/Sn ratio. Under the optimized reaction conditions, 98% glucose conversion, and 61% HMF yield were achieved over as-synthesized SnP-1 catalyst with P/Sn mole ratio of 1.0. The high catalytic activity of the SnP-1 catalyst can be attributed to its high acidity and the presence of water tolerant Bronsted and Lewis acid sites. Furthermore, the catalytic activity of SnP-1 catalyst is retained even after four cycles indicating its good catalytic stability.
机译:这项工作证明了一种简单而绿色的方法,用于合成磷酸锡(SNP)催化剂以葡萄糖转化为HMF转化。在该方法中,通过在室温下的SnCl4中心点5h(2)O和NaH2PO4中心点2H(2)O的混合物的固态研磨,然后用或干燥,通过固态研磨来制备具有各种P / Sn摩尔比的SNP催化剂。没有煅烧。使用N-2物质,XRD,FT-IR,Py-IR,NH3-TPD和XPS技术研究了所得SNP催化剂的物理化学性质。表征研究表明,不同的p / sn比对SNP催化剂的纹理和表面酸性能影响。评价这些催化剂的活性用于使用可回收的低沸点有机溶剂THF作为HMF萃取溶剂在水中脱水以进行HMF生产的葡萄糖。实验结果表明,SNP催化剂的催化活性依赖于P / Sn比。在优化的反应条件下,通过P / Sn摩尔比为1.0的合成的SNP-1催化剂,实现了98%的葡萄糖转化率和61%HMF产率。 SNP-1催化剂的高催化活性可归因于其高酸度和耐水性富棱镜和路易斯酸的存在。此外,即使在四个循环后,SNP-1催化剂的催化活性也被保留,表明其良好的催化稳定性。

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