Synthesis of Lactide from <scp>L</scp> -Lactic Acid over the Phosphoric Acid Etched Zeolite Catalyst

Polylactic acid (PLA) is a promising biodegradable polymer. However, its large-scale production is hindered by the efficient synthesis of lactide (LT), a key intermediate. In this study, we develop a simple and effective strategy to enhance the catalytic performance of H-Beta zeolite in the one-step conversion of L-lactic acid (L-LA) to LT through phosphoric acid (H3PO4) etching. A series of acid-modified Beta zeolite catalysts were prepared by systematically varying the concentration of H3PO4 and the treatment duration. Among them, the modified H-Beta zeolite (2-Beta-P) exhibited the highest catalytic activity, obtaining an LA yield of 75%. This yield is significantly higher than that of the pristine H-Beta catalyst. Comprehensive characterization results reveal that the H3PO4 treatment can selectively remove the framework aluminum, optimize the ratio of Brønsted to Lewis acid sites, while preserving the intrinsic microporous structure, thereby facilitating molecular diffusion. Kinetic studies further demonstrated that 2-Beta-P reduced the apparent activation energy from 65.8 to 44.8, indicating that surface chemical processes primarily govern the reaction. These findings highlight phosphoric acid etching as a simple yet powerful modification strategy that can significantly enhance both the activity and selectivity of H-Beta zeolites, offering valuable insights for the sustainable and efficient production of lactide.

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Journal
Industrial & Engineering Chemistry Research
Published
2026-03-02
DOI
https://doi.org/10.1021/acs.iecr.5c04656
Primary Topic
biodegradable polymer synthesis and properties
Type
article
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article

Synthesis of Lactide from L -Lactic Acid over the Phosphoric Acid Etched Zeolite Catalyst

Xi Zhang, Xiuzheng Zhuang, Longlong Ma, Yubao Chen et al.
Industrial & Engineering Chemistry Research
biodegradable polymer synthesis and properties
article

Synthesis of Lactide from L -Lactic Acid over the Phosphoric Acid Etched Zeolite Catalyst

Xi Zhang, Xiuzheng Zhuang, Longlong Ma, Yubao Chen, Xiang Yang
article en

Abstract

Polylactic acid (PLA) is a promising biodegradable polymer. However, its large-scale production is hindered by the efficient synthesis of lactide (LT), a key intermediate. In this study, we develop a simple and effective strategy to enhance the catalytic performance of H-Beta zeolite in the one-step conversion of L-lactic acid (L-LA) to LT through phosphoric acid (H3PO4) etching. A series of acid-modified Beta zeolite catalysts were prepared by systematically varying the concentration of H3PO4 and the treatment duration. Among them, the modified H-Beta zeolite (2-Beta-P) exhibited the highest catalytic activity, obtaining an LA yield of 75%. This yield is significantly higher than that of the pristine H-Beta catalyst. Comprehensive characterization results reveal that the H3PO4 treatment can selectively remove the framework aluminum, optimize the ratio of Brønsted to Lewis acid sites, while preserving the intrinsic microporous structure, thereby facilitating molecular diffusion. Kinetic studies further demonstrated that 2-Beta-P reduced the apparent activation energy from 65.8 to 44.8, indicating that surface chemical processes primarily govern the reaction. These findings highlight phosphoric acid etching as a simple yet powerful modification strategy that can significantly enhance both the activity and selectivity of H-Beta zeolites, offering valuable insights for the sustainable and efficient production of lactide.

Industrial & Engineering Chemistry ResearchVol. 65(9)
Yunnan Normal University (CN), Ministry of Education (NZ), Ministry of Education (RO), Yunnan Provincial Department of Education (CN)
Responsible consumption and production
Openalex Percentile: Top 39%
biodegradable polymer synthesis and properties
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Synthesis of Lactide from <scp>L</scp> -Lactic Acid over the Phosphoric Acid Etched Zeolite Catalyst — Xi Zhang, Xiuzheng Zhuang, et al. · Industrial & Engineering Chemistry Research (2026) | TGRS Research Map | TGRS