2007Journal of Anhui Science and Technology UniversityRequires access

Analysis of Organic Acids in Grape by Reversed Phase High Performance Liquid Chromatography

Tan Zhi-jing

Open publisher page 0 citations

Abstract

A quantitative reversed-phase high performance liquid chromatography method using diode array detector has been developed for the determination of tartaric acid,fumarate citric acid and malic acid in grape.A Hibar column was used with phosphate buffer solution(ph=2.5)as the mobile phase at a flow rate of 1.0mL/min.The column temperature was 30℃ and the UV detection wavelength was 214 nm.The calibration curve for citric acid and malic acid was in good linearity in the range of 15.0-63.4μg with the regression equation Y=1064.5X+3.58,r=0.9952,and 10-46.8μg,Y=1066.3X-4.31,r=0.9997,respectively.The average recoveries of three concentration levels for citric acid and malic acid in grape were 95.5%-96.5%and 100.2%-103.8%,respectively.RSD were 0.11%-0.38%and 0.41%-2.53%,respectively.The detection limits for citric acid and malic acid were 0.2μg and 0.1μg(S/N=3),respectively.The results indicate that this method is fast,sensitive,reproducible and practical for the routine analysis of organic acids in grape.

About this research paper

What this paper is about

A quantitative reversed-phase high performance liquid chromatography method using diode array detector has been developed for the determination of tartaric acid,fumarate citric acid and malic acid in grape.A Hibar column was used with phosphate buffer solution(ph=2.5)as the mobile phase at a flow rate of 1.0mL/min.The column temperature was 30℃ and the UV detection wavelength was 214 nm.The calibration curve for citric acid and malic acid was in good linearity in the range of 15.0-63.4μg with the regression equation Y=1064.5X+3.58,r=0.9952,and 10-46.8μg,Y=1066.3X-4.31,r=0.9997,respectively.The average recoveries of three concentration levels for citric acid and malic acid in grape were 95.5%-96.5%and 100.2%-103.8%,respectively.RSD were 0.11%-0.38%and 0.41%-2.53%,respectively.The detection limits for citric acid and malic acid were 0.2μg and 0.1μg(S/N=3),respectively.The results indicate that this method is fast,sensitive,reproducible and practical for the routine analysis of organic acids in grape.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

A quantitative reversed-phase high performance liquid chromatography method using diode array detector has been developed for the determination of tartaric acid,fumarate citric acid and malic acid in grape.A Hibar column was used with phosphate buffer solution(ph=2.5)as the mobile phase at a flow rate of 1.0mL/min.The column temperature was 30℃ and the UV detection wavelength was 214 nm.The calibration curve for citric acid and malic acid was in good linearity in the range of 15.0-63.4μg with the regression equation Y=1064.5X+3.58,r=0.9952,and 10-46.8μg,Y=1066.3X-4.31,r=0.9997,respectively.The average recoveries of three concentration levels for citric acid and malic acid in grape were 95.5%-96.5%and 100.2%-103.8%,respectively.RSD were 0.11%-0.38%and 0.41%-2.53%,respectively.The detection limits for citric acid and malic acid were 0.2μg and 0.1μg(S/N=3),respectively.The results indicate that this method is fast,sensitive,reproducible and practical for the routine analysis of organic acids in grape.

Key concepts: Citric acid, Malic acid, Tartaric acid, Calibration curve, Chromatography, High-performance liquid chromatography, Chemistry, Detection limit

Related papers

Back to paper searchBrowse research topicsOriginal source
Analysis of Organic Acids in Grape by Reversed Phase High Performance Liquid Chromatography — Research Paper | ScholarLens