Simultaneous Detection and Quantification of Organic Acids and Furans in Lignocellulosic Biomass Hydrolysate Through High-Performance Liquid Chromatography With Diode Array Detector
Patrizia Casella, Raffaele Loffredo, Maria Antonietta Rao, Federico Liuzzi, Isabella De Bari, Antonio Molino
{"title":"Simultaneous Detection and Quantification of Organic Acids and Furans in Lignocellulosic Biomass Hydrolysate Through High-Performance Liquid Chromatography With Diode Array Detector","authors":"Patrizia Casella, Raffaele Loffredo, Maria Antonietta Rao, Federico Liuzzi, Isabella De Bari, Antonio Molino","doi":"10.1002/jssc.70216","DOIUrl":null,"url":null,"abstract":"<p>Lignocellulosic biomass is gaining attention as low-cost renewable resources for sugars for fermentation and as a source of energy. Pretreatments and fermentation of these biomasses can generate organic acids and furans. Many liquid chromatography protocols have been developed for the analysis of these compounds. Organic acids are typically detected and quantified using diode array detector, while furans can be analyzed by using refractive index or ultraviolet detectors. In this work, the identification of succinic, lactic, formic, and acetic acids and two furans (5-hydroxymethylfurfural and furfural) was performed by ultra-high-performance liquid chromatography coupled with diode array detector and ion chromatography columns. Different chromatographic conditions were tested by varying the column temperature and the flow rate of sulfuric acid 5 mM. Calibration curves, peak resolution, limit of detection, and limit of quantification were calculated using analytical standards at known concentrations for each compound. The accuracy was evaluated by the recovery of the compounds in wheat straw hydrolysate. For succinic acid, the best condition was at a flow rate of 0.6 mL/min and a column temperature of 60°C while formic and lactic acids and furans were better recovered at 1.0 mL/min and 60°C.</p>","PeriodicalId":17098,"journal":{"name":"Journal of separation science","volume":"48 7","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jssc.70216","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of separation science","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jssc.70216","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Lignocellulosic biomass is gaining attention as low-cost renewable resources for sugars for fermentation and as a source of energy. Pretreatments and fermentation of these biomasses can generate organic acids and furans. Many liquid chromatography protocols have been developed for the analysis of these compounds. Organic acids are typically detected and quantified using diode array detector, while furans can be analyzed by using refractive index or ultraviolet detectors. In this work, the identification of succinic, lactic, formic, and acetic acids and two furans (5-hydroxymethylfurfural and furfural) was performed by ultra-high-performance liquid chromatography coupled with diode array detector and ion chromatography columns. Different chromatographic conditions were tested by varying the column temperature and the flow rate of sulfuric acid 5 mM. Calibration curves, peak resolution, limit of detection, and limit of quantification were calculated using analytical standards at known concentrations for each compound. The accuracy was evaluated by the recovery of the compounds in wheat straw hydrolysate. For succinic acid, the best condition was at a flow rate of 0.6 mL/min and a column temperature of 60°C while formic and lactic acids and furans were better recovered at 1.0 mL/min and 60°C.
期刊介绍:
The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.