首页> 外文期刊>Catalysts >Aqueous Dehydration, Hydrogenation, and Hydrodeoxygenation Reactions of Bio-Based Mucic Acid over Ni, NiMo, Pt, Rh, and Ru on Neutral or Acidic Catalyst Supports
【24h】

Aqueous Dehydration, Hydrogenation, and Hydrodeoxygenation Reactions of Bio-Based Mucic Acid over Ni, NiMo, Pt, Rh, and Ru on Neutral or Acidic Catalyst Supports

机译:中性或酸性催化剂载体上Ni,NiMo,Pt,Rh和Ru上生物基硫酸的水基脱水,加氢和加氢脱氧反应

获取原文
           

摘要

Hydrotreatment of mucic acid (also known as galactaric acid, an glucaric acid enantiomer), one of the most promising bio-based platform chemicals, was systematically investigated in aqueous media over alumina, silica, or carbon-supported transition (nickel and nickel-molybdenum) or noble (platinum, ruthenium and rhodium) metals. Mucic acid was only converted into mucic-1,4-lactone under non-catalytic reaction conditions in N 2 atmosphere, while the 5 MPa gaseous H 2 addition triggers hydrogenation in the bulk phase, resulting in formation of galacturonic and galactonic acid. However, dehydroxylation, hydrogenation, decarbonylation, decarboxylation, and cyclization occurred during catalytic hydrotreatment, forming various partially and completely deoxygenated products with a chain length of 3–6 C atoms. Characterization results of tested catalysts were correlated with their activity and selectivity. Insufficient pore diameter of microporous supports completely hindered the mass transfer of reactants to the active sites, resulting in negligible conversion of mucic acid. A comprehensive reaction pathway network was proposed and several industrially interesting compounds were formed, including levulinic acid, furoic acid, and adipic acid. However, selectivity towards adipic acid, a bio-based nylon 6,6 precursor, was low (up to 5 mol%) in aqueous media and elevated temperatures.
机译:粘液酸(也称为半乳糖酸,一种葡糖二酸对映体)的加氢处理是最有前途的生物基平台化学品之一,已在氧化铝,二氧化硅或碳负载的过渡态(镍和镍-钼)上的水性介质中进行了系统的研究。 )或贵金属(铂,钌和铑)。在非催化反应条件下,在N 2气氛中,仅将Mucic酸转化为mucic-1,4-lactone,而5 MPa气态H 2的添加会触发本体相中的氢化,从而形成半乳糖醛酸和半乳糖醛酸。但是,在催化加氢处理过程中发生了脱羟基,氢化,脱羰基,脱羧和环化反应,形成了链长为3-6个碳原子的各种部分和完全脱氧的产物。被测催化剂的表征结果与其活性和选择性相关。微孔载体的孔径不足完全阻碍了反应物向活性位的传质,导致粘酸的转化率可忽略不计。提出了一个全面的反应途径网络,并形成了几种工业上有意义的化合物,包括乙酰丙酸,糠酸和己二酸。但是,在水性介质和升高的温度下,对己二酸(一种生物基尼龙6,6前体)的选择性很低(最高为5 mol%)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 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