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Impact of Macroporosity on Catalytic Upgrading of Fast Pyrolysis Bio‐Oil by Esterification over Silica Sulfonic Acids

机译:大孔隙度对二氧化硅磺酸酯化快速热解生物油催化降解的影响

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摘要

Fast pyrolysis bio‐oils possess unfavorable physicochemical properties and poor stability, in large part, owing to the presence of carboxylic acids, which hinders their use as biofuels. Catalytic esterification offers an atom‐ and energy‐efficient route to upgrade pyrolysis bio‐oils. Propyl sulfonic acid (PrSO3H) silicas are active for carboxylic acid esterification but suffer mass‐transport limitations for bulky substrates. The incorporation of macropores (200 nm) enhances the activity of mesoporous SBA‐15 architectures (post‐functionalized by hydrothermal saline‐promoted grafting) for the esterification of linear carboxylic acids, with the magnitude of the turnover frequency (TOF) enhancement increasing with carboxylic acid chain length from 5 % (C3) to 110 % (C12). Macroporous–mesoporous PrSO3H/SBA‐15 also provides a two‐fold TOF enhancement over its mesoporous analogue for the esterification of a real, thermal fast‐pyrolysis bio‐oil derived from woodchips. The total acid number was reduced by 57 %, as determined by GC×GC–time‐of‐flight mass spectrometry (GC×GC–ToFMS), which indicated ester and ether formation accompanying the loss of acid, phenolic, aldehyde, and ketone components.
机译:快速热解生物油具有不利的理化性质和稳定性差,这在很大程度上是由于羧酸的存在,从而阻碍了其用作生物燃料。催化酯化提供了一种原子和能源高效的途径来升级热解生物油。丙基磺酸(PrSO3H)二氧化硅可用于羧酸酯化反应,但对于大体积的底物,其传质限制。大孔(200 nm)的引入增强了中孔SBA-15结构(通过热液盐水促进的接枝后功能化)对线性羧酸酯化的活性,周转频率(TOF)增强的幅度随羧酸的增加而增加酸链长度从5%(C3)到110%(C12)。大孔-中孔的PrSO3H / SBA-15还比其中孔类似物提供了两倍的TOF增强,可酯化来自木片的真实的热快速热解生物油。通过GC×GC-飞行时间质谱(GC×GC-ToFMS)测定,总酸值减少了57%,这表明酯和醚的形成伴随着酸,酚,醛和酮的损失组件。

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