首页> 外文期刊>ACS Sustainable Chemistry & Engineering >Matching the Activity of Homogeneous Sulfonic Acids: The Fructose-to-HMF Conversion Catalyzed by Hierarchically Porous Sulfonic-Acid-Functionalized Porous Organic Polymer (POP) Catalysts
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Matching the Activity of Homogeneous Sulfonic Acids: The Fructose-to-HMF Conversion Catalyzed by Hierarchically Porous Sulfonic-Acid-Functionalized Porous Organic Polymer (POP) Catalysts

机译:匹配均相磺酸的活性:由分层磺酸磺酸官能化多孔有机聚合物(POP)催化剂催化的果糖 - HMF转化

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摘要

Three HO3S-functionalized porous organic polymers (HO3S-POPs) with high surface areas (500-700 m(2)/g) and a broad range of porosity profiles were synthesized and tested against homogeneous-acid analogs and commercially available acid resins to evaluate their relative catalytic activities in the acid-catalyzed conversion of fructose to HMF. Comparison of fructose conversions and HMF yields demonstrates that the sulfonated POPs with hierarchical porosity can achieve catalytic activities that rival those of their homogeneous counterparts. The associated HMF selectivities represent optimized values that increase with higher temperature and faster heating, both of which can reduce the reaction time and limit product decomposition. Due to their intrinsically high mesoporosity and number of accessible acid sites, these HO3S-POPs also outperform the commercially available Amberlyst 15 resin catalyst and its crushed variant.
机译:合成具有高表面积(500-700μm(2)/ g)的三个HO3s官能化的多孔有机聚合物(HO3S-POP)和宽范围的孔隙率谱并针对均匀酸类似物和市售的酸树脂进行评估 它们在酸催化的果糖转化为HMF中的相对催化活性。 果糖转化和HMF产率的比较表明,具有等级孔隙率的磺化POP可以实现竞争活性的伴随其均匀对应物的催化活性。 相关的HMF选择性表示随着较高温度和更快的加热增加而增加的优化值,两者都可以降低反应时间和限制产品分解。 由于它们本质上高的介体和可偏转的酸位点,这些HO3S-POP也优于商业上可获得的AMBERLYST 15树脂催化剂及其碎变体。

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