Selective Chemical Conversion of Sugars in Aqueous Solutions without Alkali to Lactic Acid Over a Zn-Sn-Beta Lewis Acid-Base Catalyst

Sci Rep. 2016 May 25:6:26713. doi: 10.1038/srep26713.

Abstract

Lactic acid is an important platform molecule in the synthesis of a wide range of chemicals. However, in aqueous solutions without alkali, its efficient preparation via the direct catalysis of sugars is hindered by a side dehydration reaction to 5-hydroxymethylfurfural due to Brønsted acid, which originates from organic acids. Herein, we report that a previously unappreciated combination of common two metal mixed catalyst (Zn-Sn-Beta) prepared via solid-state ion exchange synergistically promoted this reaction. In water without a base, a conversion exceeding 99% for sucrose with a lactic acid yield of 54% was achieved within 2 hours at 190 °C under ambient air pressure. Studies of the acid and base properties of the Zn-Sn-Beta zeolite suggest that the introduction of Zn into the Sn-Beta zeolite sequentially enhanced both the Lewis acid and base sites, and the base sites inhibited a series of side reactions related to fructose dehydration to 5-hydroxymethylfurfural and its subsequent decomposition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Lactic Acid / chemical synthesis*
  • Lactic Acid / chemistry*
  • Sugars / chemistry*
  • Tin / chemistry*
  • Zeolites / chemistry*
  • Zinc / chemistry*

Substances

  • Sugars
  • Zeolites
  • Lactic Acid
  • Tin
  • Zinc