Oliveira Sara M, Lopes Teresa I M S, Tóth Ildikó V, Rangel António O S S
CBQF/Escola Superior de Biotecnologia, Universidade Católica Portuguesa, Porto, Portugal.
J Agric Food Chem. 2009 May 13;57(9):3415-22. doi: 10.1021/jf803639n.
A flow system based on the multicommutation concept was developed for the determination of free and total sulfur dioxide in table wines, exploiting gas diffusion separation and spectrophotometric detection. The system allowed the comparison of malachite green and pararosaniline chemistries, using the same manifold configuration. Free and total SO(2) were determined within the ranges 1.00-40.0 and 25.0-250 mg L(-1), at determination throughputs of 25 and 23 h(-1), respectively. Employing the malachite green reaction, detection limits of 0.3 and 0.8 mg L(-1) were attained for free and total SO(2), respectively. Pararosaniline chemistry provided detection limits of 0.6 mg L(-1) for free SO(2) and 0.8 mg L(-1) for total SO(2). Relative standard deviations better than 1.8 and 1.4% were obtained by the malachite green and pararosaniline reactions, respectively. With regard to the two tested chemistries, 18 wines were analyzed and the results achieved by the pararosaniline reaction compared better with those furnished by the recommended procedure.
基于多通道进样概念开发了一种流动系统,用于利用气体扩散分离和分光光度检测法测定餐酒中的游离二氧化硫和总二氧化硫。该系统使用相同的流路配置,可对孔雀石绿法和副品红法进行比较。游离二氧化硫和总二氧化硫的测定范围分别为1.00 - 40.0和25.0 - 250 mg L⁻¹,测定通量分别为25和23 h⁻¹。采用孔雀石绿反应时,游离二氧化硫和总二氧化硫的检测限分别为0.3和0.8 mg L⁻¹。副品红法中游离二氧化硫和总二氧化硫的检测限分别为0.6 mg L⁻¹和0.8 mg L⁻¹。孔雀石绿法和副品红法分别获得了优于1.8%和1.4%的相对标准偏差。对于两种测试方法,分析了18种葡萄酒,副品红反应得到的结果与推荐方法提供的结果相比更优。