Temperature Effect on Colorimetric Determination of Sulfur Dioxide in Dried Fruits

1961 ◽  
Vol 44 (4) ◽  
pp. 641-642
Author(s):  
D H Taylor ◽  
M W Miller ◽  
F S Nury ◽  
J E Brekke
2013 ◽  
Vol 96 (5) ◽  
pp. 1103-1108 ◽  
Author(s):  
Benjamin S Liao ◽  
Jacqueline C Sram ◽  
Darin J Files

Abstract A simple and effective anion ion chromatography (IC) method with anion exchange column and conductivity detector has been developed to determine free sulfites (SO3–2) in dried fruits processed with sulfur dioxide. No oxidation agent, such as hydrogen peroxide, is used to convert sulfites to sulfates for IC analysis. In addition, no stabilizing agent, such as formaldehyde, fructose or EDTA, is required during the sample extraction. This method uses aqueous 0.2 N NaOH as the solvent for standard preparation and sample extraction. The sulfites, either prepared from standard sodium sulfite powder or extracted from food samples, are presumed to be unbound SO3–2 in aqueous 0.2 N NaOH (pH > 13), because the bound sulfites in the sample matrix are released at pH > 10. In this study, sulfites in the standard solutions were stable at room temperature (i.e., 15–25°C) for up to 12 days. The lowest standard of the linear calibration curve is set at 1.59 μg/mL SO3–2 (equivalent to 6.36 μg/g sample with no dilution) for analysis of processed dried fruits that would contain high levels (>1000 μg/g) of sulfites. As a consequence, this method typically requires significant dilution of the sample extract. Samples are prepared with a simple procedure of sample compositing, extraction with aqueous 0.2 N NaOH, centrifugation, dilution as needed, and filtration prior to IC. The sulfites in these sample extracts are stable at room temperature for up to 20 h. Using anion IC, the sulfites are eluted under isocratic conditions with 10 mM aqueous sodium carbonate solution as the mobile phase passing through an anion exchange column. The sulfites are easily separated, with an analysis run time of 18 min, regardless of the dried fruit matrix. Recoveries from samples spiked with sodium sulfites were demonstrated to be between 81 and 105% for five different fruit matrixes (apricot, golden grape, white peach, fig, and mango). Overall, this method is simple to perform and effective for the determination of high levels of sulfites in dried fruits.


1999 ◽  
Vol 62 (2) ◽  
pp. 273-281 ◽  
Author(s):  
Márcio Raimundo Milani ◽  
José Anchieta Gomes Neto ◽  
Arnaldo Alves Cardoso

1980 ◽  
Vol 63 (6) ◽  
pp. 1314-1316 ◽  
Author(s):  
Krishan L Bajaj

Abstract A simple and accurate colorimetric method has been developed for quantitative determination of capsaicin in capsicum fruits. The method does not involve prior isolation of capsaicin from green capsicum fruits, and interference due to pigments is accounted for by determining a blank. Interfering substances are removed from red capsicum fruits by column chromatography using basic alumina as adsorbent. Capsaicin from the ethyl acetate extract of dried fruits is determined by developing a yellow complex with sodium nitrite–sodium molybdate reagent, which is read at 430 nm. Lambert-Beer’s law is obeyed in the concentration range 1.5–33.5 μg capsaicin/mL. The method is reproducible and is applicable to the rapid determination of capsaicin content.


1959 ◽  
Vol 36 (2) ◽  
pp. 193-201 ◽  
Author(s):  
Julius A. Goldbarg ◽  
Esteban P. Pineda ◽  
Benjamin M. Banks ◽  
Alexander M. Rutenburg

1917 ◽  
Vol 9 (12) ◽  
pp. 1148-1148
Author(s):  
James Withrow
Keyword(s):  

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