Universidade Federal da Bahia, Instituto de Química, Grupo de Pesquisa em Química e Quimiometria, Campus Ondina, 40170-115 Salvador, Bahia, Brazil; Instituto Nacional de Ciência e Tecnologia, INCT, de Energia e Ambiente, Universidade Federal da Bahia, 40170-115 Salvador, Bahia, Brazil.
Instituto Nacional de Ciência e Tecnologia, INCT, de Energia e Ambiente, Universidade Federal da Bahia, 40170-115 Salvador, Bahia, Brazil; Universidade do Estado da Bahia, Departamento de Ciências Exatas e da Terra, 41150-000 Salvador, Bahia, Brazil.
Talanta. 2018 Mar 1;179:810-815. doi: 10.1016/j.talanta.2017.11.070. Epub 2017 Dec 5.
This work proposes a method for the determination of free and total sulfur(IV) compounds in coconut water samples, using the high-resolution continuum source molecular absorption spectrometry. It is based on the measurement of the absorbance signal of the SO gas generate, which is resultant of the addition of hydrochloric acid solution on the sample containing the sulfating agent. The sulfite bound to the organic compounds is released by the addition of sodium hydroxide solution, before the generation of the SO gas. The optimization step was performed using multivariate methodology involving volume, concentration and flow rate of hydrochloric acid. This method was established by the sum of the absorbances obtained in the three lines of molecular absorption of the SO gas. This strategy allowed a procedure for the determination of sulfite with limits of detection and quantification of 0.36 and 1.21mgL (for a sample volume of 10mL) and precision expressed as relative standard deviation of 5.4% and 6.4% for a coconut water sample containing 38.13 and 54.58mgL of free and total sulfite, respectively. The method was applied for analyzing five coconut water samples from Salvador city, Brazil. The average contents varied from 13.0 to 55.4mgL for free sulfite and from 24.7 to 66.9mgL for total sulfur(IV) compounds. The samples were also analyzed employing the Ripper´s procedure, which is a reference method for the quantification of this additive. A statistical test at 95% confidence level demonstrated that there is no significant difference between the results obtained by the two methods.
本工作提出了一种利用高分辨率连续光源分子吸收光谱法测定椰子水中游离和总(IV)硫化合物的方法。该方法基于测量添加盐酸溶液后生成的 SO 气体的吸光度信号,该信号是含硫酸化剂样品中 SO 的结果。在生成 SO 气体之前,通过添加氢氧化钠溶液将与有机化合物结合的亚硫酸盐释放出来。优化步骤采用涉及盐酸体积、浓度和流量的多元方法进行。该方法通过在 SO 气体的三条分子吸收线中获得的吸光度总和来建立。该策略允许采用一种程序来测定亚硫酸盐,其检出限和定量限分别为 0.36 和 1.21mgL(对于 10mL 样品体积),精度表示为 5.4%和 6.4%的相对标准偏差,用于测定含有 38.13 和 54.58mgL 的游离和总亚硫酸盐的椰子水样品。该方法用于分析来自巴西萨尔瓦多市的五个椰子水样品。游离亚硫酸盐的平均含量从 13.0 到 55.4mgL 不等,总(IV)硫化合物的平均含量从 24.7 到 66.9mgL 不等。这些样品还采用 Ripper 法进行分析,该方法是定量这种添加剂的参考方法。在 95%置信水平下进行的统计检验表明,两种方法的结果无显著差异。