Method for measuring nonprotein nitrogen content in plants and plant products

A method of determination and technology of plant products, applied in the field of nitrogen analysis and determination, can solve the problems of incomplete and thorough digestion products, low recovery rate of non-protein nitrogen, inaccurate measurement results, etc., achieve simple steps, simple operation, and improved detection efficiency effect

Inactive Publication Date: 2012-06-27
CHINA TOBACCO GUANGDONG IND
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] High-pressure digestion is better for inorganic nitrogen in non-protein nitrogen, but for plant alkaloids and amino acid non-protein nitrogen, such as nicotine, theophylline, leucine, etc., due to its complex structure, high-pressure digestion is used Sometimes there is incomplete and incomplete digestion, which leads to low recovery rate of non-protein nitrogen determination and inaccurate measurement results
Especially for plants and plant products, most of their non-protein nitrogen belongs to plant alkaloids or amino acids, and plants and plant products also contain reducing components, such as sugars, and these reducing components will react with oxidants, thereby affecting the The digestion of nitrogen-containing components results in incomplete and incomplete digestion. When the above method is used to measure the non-protein nitrogen content, the digestion products obtained are not complete and thorough, resulting in inaccurate measurement results.

Method used

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  • Method for measuring nonprotein nitrogen content in plants and plant products
  • Method for measuring nonprotein nitrogen content in plants and plant products
  • Method for measuring nonprotein nitrogen content in plants and plant products

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0071]11 g of sodium nitrate was dissolved in 100 mL of distilled water to obtain a sodium nitrate stock solution with a mass concentration of 10.0%. Accurately pipette 1.0mL, 2.0mL, 4.0mL, 6.0mL, 8.0mL, and 10.0mL of the standard stock solution, and use 0.5% acetic acid solution to make up the volume to 100mL respectively to obtain a series of sodium nitrate standards to be tested solution. Take 2 mL of the standard solution to be tested respectively, and pour it into the sample tube of the continuous flow analyzer for three parallel measurements. In the continuous flow analyzer, the sample injection volume is 0.1mL / min, the injection time is 100s, and the flushing time is 120s. First at 90°C, add 2mL of potassium persulfate solution with a molar concentration of 0.3mol / L in the standard solution to be tested, the injection volume of potassium persulfate solution is 0.8mL / min, then the mixed solution obtained at 90 Under the acidic conditions provided by hydrochloric acid, ...

Embodiment 2~3

[0077] 3.2446g of nicotine was dissolved with distilled water and the volume was adjusted to 200mL to obtain a nicotine stock solution with a mass concentration of 1.60%. Pipette 16.0 mL and 32.0 mL of the nicotine stock solution, and dilute to 100 mL with 0.5% acetic acid solution by volume to obtain a nicotine solution to be tested. Pipette 2.0 mL of the two different concentrations of nicotine to be tested, and pour them into the sample tubes of the flow analyzer for three parallel measurements. In the continuous flow analyzer, the sample injection volume is 0.1mL / min, the injection time is 100s, and the flushing time is 120s. First at 90°C, 2mL of potassium persulfate solution with a molar concentration of 0.3mol / L was added to the nicotine solution to be tested, and the injection volume of the potassium persulfate solution was 0.8mL / min, and then the mixed solution obtained was Under the acidic conditions provided by hydrochloric acid at 90°C, UV lamps were irradiated fo...

Embodiment 4

[0086] 3.6032g of theophylline was dissolved in distilled water and adjusted to 100mL to obtain a stock solution of theophylline with a mass concentration of 3.48%. Pipette 5 mL of the theophylline stock solution, and dilute to 100 mL with 0.5% acetic acid solution by volume fraction to obtain the theophylline solution to be tested. Pipette 2.0 mL of the theophylline solution to be tested and pour it into the sample tube of the flow analyzer for three parallel measurements. The detection process is the same as that in Examples 2 to 3 to obtain the ultraviolet spectrum of theophylline.

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Abstract

The invention provides a method for measuring nonprotein nitrogen content in plants and plant products, which includes the following steps: separating protein nitrogen from a plant and a plant product to obtain a to-be-measured sample containing nonprotein nitrogen; adding potassium persulfate into the to-be-measured sample to obtain a mixed solution under the heating condition; performing ultraviolet catalysis and high-temperature heating to the mixed solution sequentially, so as to obtain a digestion product; detecting the digestion product to obtain ultraviolet spectrum data; and obtaining the nonprotein nitrogen content in the plant and the plant product as per the ultraviolet spectrum data and a predetermined standard curve. The method provided by the invention has excellent digestion effect, the digestion of the nonprotein nitrogen ingredient as well as the digestion of the reductive ingredient in the to-be-measured sample can be realized, the reductive function of the to-be-measured sample is lost, the interference in the nonprotein nitrogen ingredient digestion is reduced, so that the digestion effect becomes more uniform, the recovery rate of the nonprotein nitrogen measurement is improved, and the accuracy of the measurement result is improved.

Description

technical field [0001] The invention relates to the technical field of nitrogen analysis and determination, in particular to a method for determining the content of non-protein nitrogen in plants and plant products. Background technique [0002] Nitrogen is an indispensable nutrient element for plant growth and development, known as the element of life, and nitrogen metabolism plays a dominant role in plant metabolism. Nitrogen in plants can be divided into protein nitrogen and non-protein nitrogen. Protein nitrogen is the nitrogen content that plants are using; non-protein nitrogen mainly includes amino acids, alkaloids, nitrates, nitrites and ammonia salts, etc., which is a storage form nitrogen; total nitrogen represents the total nitrogen uptake by plants. The content of nitrogen in plants changes with its physiological status and environmental conditions, so measuring the content of different forms of nitrogen is very important for studying the nitrogen absorption, tra...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N21/33G01N1/44
Inventor 孔浩辉程志颖张心颖
Owner CHINA TOBACCO GUANGDONG IND
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