CN113109332A - Rapid detection reagent and method for potassium iodate in salt - Google Patents

Rapid detection reagent and method for potassium iodate in salt Download PDF

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Publication number
CN113109332A
CN113109332A CN202110398160.6A CN202110398160A CN113109332A CN 113109332 A CN113109332 A CN 113109332A CN 202110398160 A CN202110398160 A CN 202110398160A CN 113109332 A CN113109332 A CN 113109332A
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parts
salt
potassium iodate
solution
reagent
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王树庆
潘洪民
范维江
姜薇薇
刘晓芳
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Shandong Institute of Commerce and Technology
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Shandong Institute of Commerce and Technology
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    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/75Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
    • G01N21/77Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
    • G01N21/78Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour

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Abstract

The invention belongs to the technical field of salt detection, and particularly relates to a method for rapidly detecting potassium iodate in salt. The reagent adopted in the method comprises the following raw materials in parts by weight: 10-50 parts of citric acid, 5-10 parts of potassium iodide, 20-30 parts of hydrazine sulfate, 20-30 parts of starch and 1-5 parts of ethylene diamine tetraacetic acid. The method of the invention comprises the following steps: adding water into salt to dissolve, adding detection reagent, observing the color change condition of the solution, and judging whether the salt contains potassium iodate according to the color change condition of the solution. The invention has the beneficial effects that: (1) by adopting the method, whether the potassium iodate exists in the salt can be conveniently and quickly judged, and the judgment result is high in accuracy; (2) the detection reagent provided by the invention is low in cost and easy to popularize and apply in large scale. (3) The method of the invention can solve the problem of interference of nitrite in the salt, especially in the crude salt.

Description

Rapid detection reagent and method for potassium iodate in salt
Technical Field
The invention belongs to the technical field of salt detection, and particularly relates to a method for rapidly detecting potassium iodate in salt.
Background
The severity and consequences of global malnutrition have been increasingly recognized over the past decade. More than one third of the world's population is severely deficient in micronutrients, particularly iodine. In less developed countries, these defects can have serious consequences for public health, particularly for women and children.
Iodine deficiency in soil and water and food can lead to iodine deficiency. Inadequate iodine intake in the diet can lead to cretinism. Deaf-mute, goiter, leading to developmental delay, malformations, and infant and neonatal mortality. These diseases are collectively referred to as iodine deficiency (IDD), which is easily prevented by ingestion of sufficient iodine. The average daily requirement for iodine was 150 micrograms.
Iodine has particular biological significance since it is a component of the thyroid hormone thyroxine. Iodine plays a role in controlling the metabolism of the body. These hormones are also essential for normal physical growth and mental development in children.
Iodine is the most abundant in nature in the ocean, it is present in the original development stage of the earth, but a large amount of water is leached from surface soil by glaciers, snow and rain, and is washed into the sea by wind and seawater. Thus, plateau populations tend to be more iodine deficient, and the incidence of iodine deficiency is generally higher.
Fortification of commonly used foods is an important component of the strategy for the prevention and treatment of micronutrient malnutrition. Salt is an ideal carrier for micronutrients, and in particular in developing countries, common salt has proven to be an ideal carrier against micronutrient deficiencies, because of its low price, its consumption is generally uniform throughout the population class, independent of socio-economic status, and the possibility of excessive intake is low. In developed countries, iodine salts or iodized salts are already present, while in north america and most european countries, the iodine deficiency problem has been substantially eliminated. However, since the severity and severity of iodine deficiency has not been widely recognized until recently, most affected countries have only begun to take steps to popularize iodization of common salt in the last few years. Iodination programs have been enacted in many developing countries and they have begun to dramatically reduce iodine deficiency.
The salt can be potassium iodide (KI) or iodate(KIO3) The former is stable in refined dry salt and the latter shows better stability in poor salt with poor package.
The method for measuring the iodide ions in the potassium iodate salt is generally carried out according to a direct titration method in GB/T13025.7-1999 determination of iodide ions in the general test method of salt manufacturing industry, wherein in the measuring process of the method, a potassium iodate standard solution is prepared, then a sodium thiosulfate standard solution is calibrated, the titer of the sodium thiosulfate standard solution on the iodide ions is calculated, and then the sodium thiosulfate standard use solution is used for titrating the salt. Because the concentration of the titrated sodium thiosulfate is about 0.002 mol/L and is low, the titration needs to be carried out again before each batch of samples are measured, and the operation process is time-consuming. The method can only be carried out in a laboratory, and cannot meet the aim of rapid field detection.
At present, the principle for rapidly detecting potassium iodate in salt is that under an acidic condition, potassium iodate reacts with potassium iodide to quantitatively separate out iodine, the iodine and starch generate colors, the color depth is in direct proportion to the iodine content, and the iodine content can be determined by comparing the colors with a standard colorimetric card. However, this method has a fatal drawback that nitrite contained in common salt, even in a very small amount, causes a false positive result. GB 15198-. Nitrite reacts with iodide in an acidic environment, even in trace amounts, to form nitric oxide, iodine and water, and the reaction equation is as follows:
2NO2 - + 2I- + 4H+ = 2NO + I2 +2H2O
the nitrogen monoxide produced in the reaction can be oxidized into nitrite by oxygen in the air, the nitrite further reacts with iodide to generate more iodine and nitrogen monoxide, the reaction can be circulated indefinitely, and false positive results are caused. Therefore, only elimination of nitrite can avoid the generation of false positive results.
Therefore, the present invention is needed to improve the above-mentioned drawbacks and to provide a reagent and a method for rapidly detecting potassium iodate in common salt, which can remove the nitrite in common salt to avoid the occurrence of false positive result.
Disclosure of Invention
In order to solve the technical problems, the invention avoids the occurrence of false positive results by removing nitrite in the salt, thereby providing a rapid detection reagent for potassium iodate in the salt, which has high accuracy, low detection cost and short detection time;
the invention provides a rapid detection reagent for potassium iodate in salt, which comprises the following raw materials in parts by weight:
the quick detection reagent for potassium iodate in salt comprises the following raw materials in parts by weight:
10-50 parts of citric acid, 5-10 parts of potassium iodide, 20-30 parts of hydrazine sulfate, 20-30 parts of starch and 1-5 parts of ethylene diamine tetraacetic acid.
The reagent comprises the following raw materials in parts by weight:
10-40 parts of citric acid, 5-8 parts of potassium iodide, 22-28 parts of hydrazine sulfate, 22-28 parts of starch and 1-5 parts of ethylene diamine tetraacetic acid.
The reagent comprises the following raw materials in parts by weight:
25 parts of citric acid, 7 parts of potassium iodide, 25 parts of hydrazine sulfate, 25 parts of starch and 3 parts of ethylenediamine tetraacetic acid.
Preferably, the method for rapidly detecting potassium iodate in salt comprises the following steps:
s1: taking salt, pouring into a test tube, and adding water to dissolve the salt to obtain a salt solution;
s2: preparing a reagent:
taking the following raw materials in parts by weight: 10-50 parts of citric acid, 5-10 parts of potassium iodide, 20-30 parts of hydrazine sulfate, 20-30 parts of starch and 1-5 parts of ethylene diamine tetraacetic acid, and uniformly mixing;
s3: adding the reagent in the S2 into the salt solution of the S1, shaking up, and observing the color change condition of the solution;
s4: observing the mixed solution in the S3, and if the solution is bluish purple, judging that the salt contains potassium iodate; if the color of the solution is not changed, the salt is judged to have no potassium iodate.
Preferably, S1: taking salt, adding water to dissolve the salt, wherein the mass volume ratio of the salt to the water is 1g/3 mL.
The method for rapidly detecting the potassium iodate in the salt comprises the following steps:
s1: taking salt, adding water to dissolve the salt, wherein the mass volume ratio of the salt to the water is 1g/3 mL;
s2: preparing a reagent:
taking the following raw materials in parts by weight: 10-50 parts of citric acid, 5-10 parts of potassium iodide, 20-30 parts of hydrazine sulfate, 20-30 parts of starch and 1-5 parts of ethylene diamine tetraacetic acid, and uniformly mixing;
s3: adding the reagent in the S2 into the salt solution of the S1, shaking up, and observing the color change condition of the solution;
s4: observing the mixed solution in the S3, and if the solution is bluish purple, judging that the salt contains potassium iodate; if the color of the solution is not changed, the salt is judged to have no potassium iodate.
The invention has the beneficial effects that:
(1) by adopting the method, whether the potassium iodate exists in the salt can be conveniently and quickly judged, and the judgment result is high in accuracy;
(2) the detection reagent has low cost and is easy to popularize and apply in large scale;
(3) the method of the invention can solve the interference problem of nitrite in salt, especially in crude salt.
Drawings
FIG. 1 is a photograph of starch discoloration caused by reaction of nitrite with potassium iodide under acidic conditions;
FIG. 2 is a photograph of the discoloration of starch by the reaction of potassium iodate with potassium iodide under acidic conditions.
Detailed Description
The present invention will now be further described with reference to specific embodiments in order to enable those skilled in the art to better understand the present invention.
Example 1
The quick detection reagent for potassium iodate in salt is prepared by the following steps: taking the following raw materials in parts by weight:
25 parts of citric acid, 7 parts of potassium iodide, 25 parts of hydrazine sulfate, 25 parts of starch and 3 parts of ethylene diamine tetraacetic acid, and uniformly mixing to obtain the detection reagent.
Example 2
The quick detection reagent for potassium iodate in salt is prepared by the following steps: taking the following raw materials in parts by weight:
15 parts of citric acid, 10 parts of potassium iodide, 20 parts of hydrazine sulfate, 20 parts of starch and 1 part of ethylene diamine tetraacetic acid, and uniformly mixing to obtain the detection reagent.
Example 3
The quick detection reagent for potassium iodate in salt is prepared by the following steps: taking the following raw materials in parts by weight:
50 parts of citric acid, 5 parts of potassium iodide, 30 parts of hydrazine sulfate, 30 parts of starch and 5 parts of ethylene diamine tetraacetic acid, and uniformly mixing to obtain the detection reagent.
Example 4
The method for rapidly detecting the potassium iodate in the salt comprises the following steps:
s1: 1g of salt is taken and poured into a test tube, and 3mL of water is added to dissolve the salt to obtain a sample 1 to be detected; then preparing the same samples 2 and 3 according to the method;
s2: 0.1g of the reagents prepared in the examples 1, 2 and 3 are respectively added into three salt sample solutions of S1, shaken up and the color change of the solutions is observed;
s3: observing the mixed solution in S3, and if the solution is bluish purple, indicating that the salt contains potassium iodate; if the color of the solution is not changed, the salt is said to have no potassium iodate.
Example 5
Influence of nitrite on the assay results
In the potassium iodide solution, nitrite with different concentrations was added, then hydrochloric acid with 0.1N concentration was used to adjust the acidity of the solution, and then the reaction of trace amount of nitrite with iodide in the solution was observed, and the results are shown in table 1.
TABLE 1 influence of nitrite on the results
NO2 -(M) I-(M) H+(M) Color change condition
4.1×10-6 1.1×10-2 0 Discolouring after 1hr
8.5×10-6 1.1×10-2 0 Discolouring after 1hr
0 1.1×10-2 0.6 Color change in about 4 minutes
4.1×10-6 1.1×10-2 0.6 Discolouration after 1 second
8.5×10-6 1.1×10-2 0.6 Discolouration after 1 second
As can be seen from table 1, under acidic conditions, nitrite also reacts rapidly with iodide, thereby discoloring starch, indicating that the presence of trace amounts of nitrite inevitably affects the detection of potassium iodide under acidic conditions.
Example 6
Determination of Potassium iodate
The specific method comprises the following steps:
s1: three portions of analytically pure sodium chloride solid are taken as base materials, 30mg/kg of potassium iodate is added into the first portion, and the first portion is marked as a sample A; the second portion was added with 5mg/kg of sodium nitrite and was designated sample B; the third portion was designated as C as a control.
S2: respectively taking A, B, C samples of 1g, dissolving with 3mL of water to obtain a salt solution to be detected;
s3: adding the reagents prepared in example 1 into the common salt solution to be detected respectively, observing the color change condition of the solution, wherein the mass ratio of the added amount of the reagents to the common salt is 1: 10; the results of the color change of the solution are shown in Table 2.
TABLE 2 color change of saline solution for different treatments
Sample (I) Treatment of Color change of solution
Sample A Potassium iodate and sodium chloride Blue color
Sample B Nitrite + sodium chloride No color change
Sample C Sodium chloride No color change
As can be seen from Table 2, in the combined potassium iodate and sodium chloride solution, the color of the solution appeared blue; in the solution of the nitrite and sodium chloride combination, the solution has no color change; in the sodium chloride solution in sample C, the solution did not change color. This shows that the method of the present invention completely eliminates the interference of nitrite during the determination of potassium iodate.

Claims (7)

1. The reagent for rapidly detecting potassium iodate in table salt is characterized by comprising the following raw materials in parts by weight:
10-50 parts of citric acid, 5-10 parts of potassium iodide, 20-30 parts of hydrazine sulfate, 20-30 parts of starch and 1-5 parts of ethylene diamine tetraacetic acid.
2. The reagent for rapidly detecting potassium iodate in common salt as claimed in claim 1, wherein the reagent comprises the following raw materials by weight:
10-40 parts of citric acid, 5-8 parts of potassium iodide, 22-28 parts of hydrazine sulfate, 22-28 parts of starch and 1-5 parts of ethylene diamine tetraacetic acid.
3. The reagent for rapidly detecting potassium iodate in common salt as claimed in claim 1, wherein the reagent comprises the following raw materials by weight:
25 parts of citric acid, 7 parts of potassium iodide, 25 parts of hydrazine sulfate, 25 parts of starch and 3 parts of ethylenediamine tetraacetic acid.
4. The method for rapidly detecting potassium iodate in common salt as claimed in claim 1, comprising the steps of:
s1: taking salt, pouring into a test tube, and adding water to dissolve the salt to obtain a salt solution;
s2: preparing a reagent:
taking the following raw materials in parts by weight: 10-50 parts of citric acid, 5-10 parts of potassium iodide, 20-30 parts of hydrazine sulfate, 20-30 parts of starch and 1-5 parts of ethylene diamine tetraacetic acid, and uniformly mixing;
s3: adding the reagent in the S2 into the salt solution of the S1, shaking up, and observing the color change condition of the solution;
s4: observing the mixed solution in the S3, and if the solution is bluish purple, judging that the salt contains potassium iodate; if the color of the solution is not changed, the salt is judged to have no potassium iodate.
5. The method for rapidly detecting potassium iodate in common salt as claimed in claim 1, wherein the reaction mixture is a mixture of potassium iodate and sodium chloride,
s1: taking salt, adding water to dissolve the salt, wherein the mass volume ratio of the salt to the water is 1g/3 mL.
6. The method for rapidly detecting potassium iodate in common salt as claimed in claim 1, wherein the reaction mixture is a mixture of potassium iodate and sodium chloride,
in S3, the mass ratio of the reagent in S2 to the common salt in S1 is 1: 10.
7. the method for rapidly detecting potassium iodate in common salt as claimed in claim 1, comprising the steps of:
s1: taking salt, adding water to dissolve the salt, wherein the mass volume ratio of the salt to the water is 1g/3 mL;
s2: preparing a reagent:
taking the following raw materials in parts by weight: 10-50 parts of citric acid, 5-10 parts of potassium iodide, 20-30 parts of hydrazine sulfate, 20-30 parts of starch and 1-5 parts of ethylene diamine tetraacetic acid, and uniformly mixing;
s3: adding the reagent in the S2 into the salt solution of the S1, shaking up, and observing the color change condition of the solution; the mass ratio of the reagent in the S2 to the common salt in the S1 is 1: 10;
s4: observing the mixed solution in the S3, and if the solution is bluish purple, judging that the salt contains potassium iodate; if the color of the solution is not changed, the salt is judged to have no potassium iodate.
CN202110398160.6A 2021-04-14 2021-04-14 Rapid detection reagent and method for potassium iodate in salt Pending CN113109332A (en)

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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1178322A (en) * 1996-09-27 1998-04-08 李全水 Simple and rapid field monitoring method for iodine content of potassium iodate-added salt
CN101413894A (en) * 2008-11-24 2009-04-22 张质毅 Iodine content on site rapid quantitative detection reagent in common salt added with iodine and preparation process thereof
CN202159014U (en) * 2011-08-03 2012-03-07 吴娅 Illegal cooking oil verification device
CN103472057A (en) * 2013-09-25 2013-12-25 哈尔滨医科大学 Rapid iodized salt detection liquid
CN106536481A (en) * 2014-06-19 2017-03-22 梅里亚股份有限公司 Parasiticidal compositions comprising indole derivatives, methods and uses thereof
CN108007927A (en) * 2017-12-12 2018-05-08 江苏盐城环保科技城重金属防治研究中心 A kind of method that manganese content in manganese slag is detected using EDTA proportion optimization designs
CN110044891A (en) * 2019-05-13 2019-07-23 山东省食品药品检验研究院 A kind of detection method of amino acid iodine content of iodine

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1178322A (en) * 1996-09-27 1998-04-08 李全水 Simple and rapid field monitoring method for iodine content of potassium iodate-added salt
CN101413894A (en) * 2008-11-24 2009-04-22 张质毅 Iodine content on site rapid quantitative detection reagent in common salt added with iodine and preparation process thereof
CN202159014U (en) * 2011-08-03 2012-03-07 吴娅 Illegal cooking oil verification device
CN103472057A (en) * 2013-09-25 2013-12-25 哈尔滨医科大学 Rapid iodized salt detection liquid
CN106536481A (en) * 2014-06-19 2017-03-22 梅里亚股份有限公司 Parasiticidal compositions comprising indole derivatives, methods and uses thereof
CN108007927A (en) * 2017-12-12 2018-05-08 江苏盐城环保科技城重金属防治研究中心 A kind of method that manganese content in manganese slag is detected using EDTA proportion optimization designs
CN110044891A (en) * 2019-05-13 2019-07-23 山东省食品药品检验研究院 A kind of detection method of amino acid iodine content of iodine

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
仇厚芳: "碘盐湿法加工中碘酸钾溶液配制实验研究", 《安徽预防医学杂志》 *
宋悦等: "影响食盐中碘含量检测结果准确性的主要因素", 《农产品加工》 *
朱珮珣等: "淀粉作显色剂吸光光度法测食盐中碘酸钾", 《理化检验》 *
梁红,周清主编: "《工业分析 修订版》", 28 February 2010, 北京:中国环境科学出版社 *
赵河清等: "一种碘盐半定量检测包应用实验研究", 《地方病通报》 *
陈启丰: "碘酸钾加碘盐简介", 《广东卫生防疫》 *
马卫兴: "快速比色法测定食盐中的碘酸钾", 《检验技术》 *

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Application publication date: 20210713