首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Production of high carbon number hydrocarbon fuels from a lignin-derived α-O-4 phenolic dimer, benzyl phenyl ether, via isomerization of ether to alcohols on high-surface-area silica-alumina aerogel catalysts
【24h】

Production of high carbon number hydrocarbon fuels from a lignin-derived α-O-4 phenolic dimer, benzyl phenyl ether, via isomerization of ether to alcohols on high-surface-area silica-alumina aerogel catalysts

机译:通过木质素衍生的α-O-4酚二聚体,苄基苯基醚在高表面积二氧化硅-氧化铝气凝胶催化剂上将醚异构化成醇来生产高碳数烃燃料

获取原文
获取原文并翻译 | 示例
           

摘要

Two-step hydrodeoxygenation of benzyl phenyl ether (BPE), a lignin-derived phenolic dimer containing an α-O-4 linkage, was performed to produce high carbon number saturated hydrocarbons. The ether linkage of BPE was first isomerized to alcohols of benzylphenols on the solid acid catalysts of silica (SA), alumina (AA), and silica-alumina aerogels (SAAs), which were further hydrodeoxygenated to saturated cyclic hydrocarbons on a silica-alumina-supported Ru catalyst. During the isomerization of BPE, noble-metal-free catalysts suppressed the formation of phenyl monomers but produced the phenolic dimers. SA, AA, and SAA-73 (Al/(Si+Al)=0.73) exhibited negligible activity. However, SAA-38 and SAA-57 containing Al/(Si+Al) contents of 0.38 and 0.57, respectively, exhibited high catalytic activity among the prepared aerogel catalysts. The BPE conversion on SAA-38 reached 100% at a temperature range of 100-150 °C. The Bronsted acid sites appear to be catalytic active sites. On the basis of the predominant isomerization of phenyl ether to phenols over ether decomposition on the SAAs, the following second step of hydrodeoxygenation (HDO) after the first step of isomerization of BPE produced deoxygenated C13-19 cyclic hydrocarbons, as opposed to the saturated deoxygenated cyclic hydrocarbons produced trhough a one-step reaction process with silica-alumina-supported Ru catalysts, demonstrating this to be a promising process for producing high carbon number hydrocarbons from lignin dimers and oligomers.
机译:进行了苄基苯醚(BPE)(一种木质素衍生的含α-O-4键的酚二聚体)的两步加氢脱氧反应,以生产高碳数的饱和烃。首先,在二氧化硅(SA),氧化铝(AA)和二氧化硅-氧化铝气凝胶(SAA)的固体酸催化剂上,将BPE的醚键异构化为苄基酚的醇,再将其进一步加氢脱氧为二氧化硅-氧化铝上的饱和环状烃负载的Ru催化剂。在BPE的异构化过程中,不含贵金属的催化剂抑制了苯基单体的形成,但生成了酚二聚体。 SA,AA和SAA-73(Al /(Si + Al)= 0.73)的活性可忽略不计。然而,在所制备的气凝胶催化剂中,分别具有0.38和0.57的Al /(Si + Al)含量的SAA-38和SAA-57表现出高催化活性。在100-150°C的温度范围内,SAA-38上的BPE转化率达到100%。布朗斯台德酸位点似乎是催化活性位点。在SAA上苯醚在醚分解过程中主要异构化为苯酚,随后的第二步加氢脱氧(HDO)在BPE异构化的第一步之后生成了脱氧的C13-19环烃,与饱和的脱氧相反环状烃通过一步法与二氧化硅-氧化铝负载的Ru催化剂反应制得,证明这是一种从木质素二聚体和低聚物生产高碳数烃的有前途的方法。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号