DETERMINATION OF NITRATE CONTENT IN PRODUCTS FROM STORES IN NORILSK

Author(s):  
Alexey A. Cheremisin ◽  
Tatiana I. Vakulenko ◽  
Rimma K. Rahimova ◽  
Anton V. Kaverzin
Keyword(s):  
1975 ◽  
Vol 58 (5) ◽  
pp. 915-919 ◽  
Author(s):  
Sandra L Pfeiffer ◽  
Jean Smith

Abstract The nitrate electrode has been utilized in the determination of nitrate content in food products. The AOAC xylenol method was employed for comparative results. A reasonable correlation (r = 0.91) was found between the 2 methods in the analysis of 49 samples containing 30–350 ppm nitrate. At the average nitrate content (100 ppm) of these foods, the standard error was 4.3 ppm. The electrode responds directly to the ionic activity of the nitrate ion. It has a linear concentration range of 1–6000 ppm nitrate and can be used over a wide pH range. The electrode does respond to some extent to anions other than nitrate, and some interferences do occur. These interferences are easily controlled by the use of cation exchange resins. The Corning known addition (spiking) method is used on all samples to insure correct electrode response in solutions containing variable background ionic composition. The electrode has the advantage of simplicity, speed, reproducibility, and accuracy. Work time saved using the electrode as opposed to the xylenol method is about 7 hr for the analysis of 20 samples. Error, and the need for repeating analysis, is much less frequent.


2006 ◽  
Vol 89 (3) ◽  
pp. 712-719 ◽  
Author(s):  
Giovanna Saccani ◽  
Enrica Tanzi ◽  
Silvano Cavalli ◽  
Jeff Rohrer

Abstract The endogenous nitrate concentration in fresh meat and the residual nitrate and nitrite contents after curing are related to food quality and safety. Most ion chromatography (IC) methods suffer from interferences, especially in fresh meat samples, in which the endogenous nitrate content is low, and in cured meat products, in which other nitrogenous compounds can interfere with the separation of inorganic anions. One of the major classes of interfering compounds in fresh meat are sugar phosphates, which originate from glycolysis during the conversion of muscle glycogen to lactic acid. Nitrate can be separated from interfering compounds with a high-capacity anion-exchange column that was manufactured for use with hydroxide eluents (i.e., hydroxide-selective). This column has a different selectivity than traditional IC columns that use carbonate eluents and facilitates the determination of nitrate in both fresh and cured meats. Nitrate was detected by both suppressed conductivity measurement and mass spectrometry (MS). The identifications of nitrate and glucose-6-phosphate were confirmed by MS detection. The described IC/MS method is robust, sensitive to nitrate concentrations as low as 0.10 mg/kg, and can determine sugar phosphates that are useful for monitoring meat freshness. We successfully used this method to determine nitrate in nearly 100 muscle tissues and cured meat samples.


2006 ◽  
Vol 94 (4) ◽  
pp. 505-515 ◽  
Author(s):  
B.R. Jahn ◽  
R. Linker ◽  
S.K. Upadhyaya ◽  
A. Shaviv ◽  
D.C. Slaughter ◽  
...  

1939 ◽  
Vol 17d (6) ◽  
pp. 125-136 ◽  
Author(s):  
W. H. White

An extract suitable for the quantitative determination of nitrite, nitrate, and chloride in cured meat was prepared by freezing and thawing the sample, followed by extraction with hot water. The sulphanilic acid-α-naphthylamine hydrochloride method, applied to the photoelectric colorimeter, was suitable for the determination of nitrite in meat extract and curing pickle. A number of factors that affect this reaction were investigated. The nitrate content of cured meat and curing pickle was determined by the phenoldisulphonic acid method, slightly modified and applied to the photoelectric colorimeter. The chloride content of meat extract was determined, either by direct titration with potassium chromate as indicator, or by Volhard's procedure, after the removal of protein by ignition or wet oxidation. The latter method should be used if accuracy within 5% is desired. Direct titration was satisfactory for the determination of chloride in curing pickle.The precision of the above methods is illustrated by the following average deviations of individual determinations from their means, as computed from 25 or more duplicate determinations, and expressed as a percentage of the amount present, for meat and pickle respectively: chloride, ±0.20% and ±0.02%; nitrate ±0.70% and ±0.30%; nitrite, ±1.7% and ±0.1%.


Author(s):  
М. М. Харитонов ◽  
О. М. Лазарєва ◽  
С. М. Лемішко

Метою роботи є кількісне визначення вмісту ніт-ратів в овочевій і плодово-ягідній продукції після про-ведення польових дослідів у Дніпропетровській облас-ті. Наведено результати визначення нітратів в ово-чах, плодах і ягодах, що найчастіше використовуютьу раціоні харчування людини. Контроль вмісту ніт-ратів здійснювався потенціометричним методом звикористанням іоноселективного електроду. У ре-зультаті проведених досліджень встановлено найбіль-ше перевищення ГДК в таких овочах: редис, буряк,морква і кабачки – із 6 проб 5 перевищують ГДК. Підчас визначення вмісту нітратів у картоплі 12 проб із46 перевищували ГДК, у капусті – 2 проби з 12, а уперці – 2 проби з 9 перевищували ГДК. За вмістомнітратів вивчені в нашій роботі фрукти та ягодивідносяться до групи за малою концентрацією – до100 мг/кг. Найменший вміст нітратів знайдено у зе-леному горошку. The aim of this work is the ecological assessment of quantitative determination of nitrate in vegetable and fruit production after conducting field experiments in Dnipropetrovsk region. The results of the determination of nitrates in vegetables, fruits and berries, which are most often used in the human diet are presented. Control of nitrate content was carried out by potentiometric method using an ion-selective electrode. The results of the research showed the greatest exceedance in such vegetables: radishes, beets, carrots and pumpkin – in 6 samples 5 exceed MPC. In the determination of nitrate content in potato 12 samples from 46 exceed the MCL, in cabbage – 2 samples of 12, and pepper – in 2 samples from 9 exceed the MPC. The fruits and berries studied in our work on the nitrate concentration belong to the group of low concentration (up to 100 mg/kg). The lowest nitrate content was found in green peas.


2013 ◽  
Vol 4 (2) ◽  
pp. 47-51
Author(s):  
I.I. Mykaylo ◽  
M.V. Kryvtsova ◽  
V.I. Nikolaichuk

The aim of our research was to conduct a monitoring study of nitrate content in plant products of Uzhgorod district and to accomplish comparative analysis of the survey results in different periods of crop ripening. Selection of vegetable samples was carried out in Uzhgorod district in the early spring and summer periods. Determination of the nitrate content was performed using an ion-selective method at the Chemical and Toxicological Department of the Regional State Veterinary Medicine Laboratory in the Transcarpathian region of Ukraine. Vegetables were tested for nitrate content using the ion-selective method with the laboratory ion meter AI-123. Core investigation samples were crushed and homogenized. A 10.0 g weight of the investigated product, which was prepared according to MIR № 5048-89, was placed in a flat-bottomed or a conical flask, which was then filled with 50 cm3 potassium alumens solution and shaken in a shaking-machine for 5 minutes and then transferred into a measuring glass. The nitrate weight fraction in milligrams per kilogram was obtained together with the weight concentration value of nitrate ions in solution. For our study we selected vegetables grown in both public and private gardens of Uzhgorod district, namely: common onions, radishes, garden parsley, cucumbers, tomatoes, bell peppers, white cabbages, carrots and table beets. 25 samples were selected for each type of vegetable. Nitrate content was determined in the early spring growing period (from February 9 to May 27, 2011) and in the summer growing period (from June 3 to September 28, 2011), because in these particular periods we recorded the most frequent cases of food poisoning from nitrates among the population of the region. A clear trend has been traced towards increasing the nitrate content in food plant production, at levels which exceed the maximum permissible concentration (MPC). The results of our research demonstrate that the nitrate content exceeded the maximum permissible concentration in 9 kinds of vegetables out of the 11 selected for the investigation, which composes 82% of total production. In particular, among the selected vegetables an excess of nitrate content, above MPC was recorded in 100% of cucumbers, 92% of carrots, 40% samples of green onions, 40% of radishes, 40% of tomatoes, 28% bell peppers, and 16% of early white cabbages. However, the most significant nitrate excess, which was more than double the MPC, was observed in 56% of cucumbers, 20% of tomatoes, 8% of radishes in the early spring period and 4% of tomatoes in the summer period. Consequently, it has been established that the consumption of early vegetable production contributes to the ingestion by humans of significant amounts of nitrates. The application of an agrochemical system based upon sound measurement of the nitrate content would allow us to solve the task of increasing soil fertility and to form a deficit-free and positive balance of biogenic elements and humus in the "soil – plant – fertilizer" system and develop a system of crop production which is balanced in its chemical composition and nutritional value. To sum up, detailed determination of the factors that lead to the accumulation of nitrates in vegetable crops and the development of methods to reduce nitrate concentrations in crop production require further investigation.


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