Dried Fruits Stability, Modified Direct Colorimetric Method for Determination of Sulfur Dioxide in Dried Fruits

1959 ◽  
Vol 7 (5) ◽  
pp. 351-353 ◽  
Author(s):  
F. S. Nury ◽  
D. H. Taylor ◽  
J. E. Brekke
1965 ◽  
Vol 48 (4) ◽  
pp. 796-801
Author(s):  
F S Nury ◽  
H R Bolin

Abstract Sulfur dioxide analysis by official (Monier-Williams) methods was compared with a new colorimetric procedure for dried fruits. Dried peaches, pears, apples and golden raisins were the test materials. The colorimetric method was found to be neither more nor less variable than two official methods except in analysis of dried pears, took less time and was easier to perform than the official methods, and yielded satisfactory recovery of sulfur dioxide.


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.


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.


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

1986 ◽  
Vol 51 (10) ◽  
pp. 2077-2082 ◽  
Author(s):  
Jan Langmaier ◽  
František Opekar

Gold porous membrane electrode has been used for the potentiometric determination of small amounts of sulfur dioxide absorbed in the solutions of sodium tetrachloromercurate or sodium hydroxide. Sulfur dioxide is released by the reaction with an acid into a stream of nitrogen and led to the electrode immersed into the solution of iodine monochloride. Part of SO2 penetrates through the membrane pores into the solution where it is oxidized. The electrode redox potential change is a measure of the SO2 concentration in the absorption solution. In the solution of 1 . 10-5 M[ICl2]- in 0.02 M-HClO4 the limit of quantitation was found to be 0.07 ng SO2 . ml-1. The relative standard deviations of 1.4% and 2.5% were found for the determinations of 10 ng and 0.5 ng of SO2, respectively. Higher concentrations of H2S interfere only in the hydroxide solution. About 10 samples can be analyzed per one hour.


1990 ◽  
Vol 10 (1) ◽  
pp. 89-92 ◽  
Author(s):  
Liliane Larpent ◽  
Christian Verger

The fate of the peritoneal membrane on continuous ambulatory peritoneal dialysis (CAPD) is usually evaluated through the modification of its permeability to various solutes as glucose, creatinine, and urea. Therefore, the accuracy of the methods used for measurements of creatinine is of great importance. A particular problem does exist for creatinine determination as it may be influenced by the presence of glucose. We studied a new enzymatic colorimetric method for creatinine determination in peritoneal dialysis solutions which contain high dextrose concentrations. Creatinine was measured in plasma, urine, and dialysate from 18 patients on CAPD and in pure dextrose solutions, with an enzymatic test (Boehringer Mannheim) and with Jaffe's reaction on two different analyzers: Astra (Beckman) and Eris (Merck). Creatinine results were similar with both assays (Jaffe's reaction and enzymatic test) when measured in blood and urine. However the Jaffe's reaction gave higher creatinine results than the enzymatic test (p < 0.001), when assays were performed in peritoneal dialysis solutions and in pure glucose solutions. In addition, it appeared that other components of dialysis solutions, mainly calcium chloride, influenced unpredictably the results of creatinine with the Jaffe's reaction. We conclude that specific enzymatic test is a more accurate and reliable method to evaluate creatinine kinetics through the peritoneal membrane when determined in CAPD solutions.


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