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GB 5009.18-2025 PDF English

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GB 5009.18-2025: National food safety standard - Determination of fluorine in foods
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GB 5009.18: Evolution and historical versions

Standard IDContents [version]USDSTEP2[PDF] deliveryName of Chinese StandardStatus
GB 5009.18-2025English140 Add to Cart 0-9 seconds. Auto-delivery National food safety standard - Determination of fluorine in foods Valid
GB/T 5009.18-2003English70 Add to Cart 0-9 seconds. Auto-delivery Determination of fluorine in foods Valid
GB/T 5009.18-1996English239 Add to Cart 2 days Method for determination of fluorine in foods Obsolete
GB 5009.18-1985English239 Add to Cart 2 days Method for determination of fluorine in foods Obsolete

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GB 5009.18-2025: National food safety standard - Determination of fluorine in foods

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GB NATIONAL STANDARD OF THE PEOPLE’S REPUBLIC OF CHINA National Food Safety Standard - Determination of Fluorine in Foods Issued on. MARCH 16, 2025 Implemented on. SEPTEMBER 16, 2025 Issued by. National Health Commission of the People’s Republic of China; State Administration for Market Regulation.

Table of Contents

Foreword... 3 1 Scope... 4 Method I - Ion Chromatography... 4 2 Principle... 4 3 Reagents and Materials... 4 4 Instruments and Equipment... 6 5 Analytical Steps... 6 6 Expression of Analytical Results... 8 7 Precision... 9 8 Others... 9 Method II - Fluoride Ion Selective Electrode Method... 9 9 Principle... 9 10 Reagents and Materials... 9 11 Instruments and Equipment... 11 12 Analytical Steps... 11 13 Expression of Analytical Results... 12 14 Precision... 12 15 Others... 12 Appendix A Ion Chromatograms... 13

Foreword

This Standard replaces GB/T 5009.18-2003 Determination of Fluorine in Foods. In comparison with GB/T 5009.18-2003, the main changes are as follows. ---The title of the Standard is modified into National Food Safety Standard - Determination of Fluorine in Foods; ---The scope of application of the Standard is modified; ---Method I - ion chromatography is added; ---The previous first method, diffusion-fluorine reagent colorimetric method, and the second method, ashing distillation-fluorine reagent colorimetric method, are deleted; ---The previous third method, fluoride ion selective electrode method is adjusted to the second method, the linear range of the method is modified, and the method quantitative limit is added. National Food Safety Standard - Determination of Fluorine in Foods

1 Scope

This Standard specifies the determination method for fluorine in foods. The first method of this Standard is applicable to the determination of fluoride content in foods other than table salt and brick tea, and the second method is applicable to the determination of fluoride content in brick tea. Method I - Ion Chromatography

2 Principle

The fluorine in the specimen is fixed with alkali, ashed at high temperature, and converted into the form of salt. Under neutral or weakly alkaline conditions, it is separated by ion exchange chromatography column, determined by electrical conductivity detector, and quantified by the external standard method.

3 Reagents and Materials

Unless otherwise specified, all reagents used in this Method are guaranteed reagents, the water is Grade-1 water specified in GB/T 6682, and all utensils used are made of plastic (polyethylene or polypropylene). 3.1 Reagents 3.1.1 Potassium hydroxide (KOH). 3.2 Preparation of Reagents 3.2.1 Eluent (sodium carbonate 8.0 mmol/L and sodium bicarbonate 0.25 mmol/L). weigh-take 0.848 g of sodium carbonate and 0.021 g of sodium bicarbonate, dissolve them in an appropriate amount of water, and reach a constant volume of 1,000 mL. 3.4 Preparation of Standard Solutions 3.4.1 Fluorine standard stock solution (1,000 mg/L). accurately weigh-take 0.2210 g (accurate to 0.0001 g) of sodium fluoride dried to constant weight at 95 C ~ 105 C into a beaker, use water to dissolve it, transfer it to a 100 mL volumetric flask, add water to a constant volume, and mix it well. At 0 C ~ 4 C, store it sealed and away from light, and it shall remain valid for 6 months. 3.4.2 Fluorine standard intermediate solution (10.0 mg/L). accurately transfer-take 1.00 mL of fluorine standard stock solution (1,000 mg/L) into a 100 mL volumetric flask, add water to a constant volume and mix it well. At 0 C ~ 4 C, store it sealed and away from light, and it shall remain valid for 1 month. 3.5 Materials 3.5.1 Strong acid cation exchange resin. H type (2.5 mL). 3.5.2 Syringe. 2.5 mL or 5.0 mL. 3.5.3 0.45 m aqueous membrane syringe filter.

4 Instruments and Equipment

4.1 Ion chromatograph. equipped with electrical conductivity detector and suppressor. 4.2 Balance. the division value is respectively 0.0001 g and 0.001 g. 4.5 Muffle furnace. 4.6 High-speed pulverizer. 4.7 Homogenizer.

5 Analytical Steps

NOTE. all plastic utensils and nickel crucibles need to be soaked in sodium hydroxide solution (100 g/L) overnight, repeatedly rinsed with tap water, and finally rinsed with water. 5.1 Preparation of Specimens 5.1.1 Solid specimens 5.2 Specimen Pre-treatment 5.2.1 Specimen extraction Accurately weigh-take 0.5 g ~ 1.0 g (accurate to 0.001 g) of solid, semi-solid or solid-liquid mixed specimen or accurately transfer-take 1.00 mL ~ 2.00 mL of liquid specimen and place it in a nickel crucible, 5.3 Instrument Reference Conditions 5.3.1 Hydroxide elution system 5.3.1.1 Chromatographic columns. analytical column (250 mm  4 mm, particle size 5 m) and guard column (50 mm  4 mm, particle size 5 m), with quaternary ammonium polystyrene resin as the filler or others with equivalent performance. 5.3.2.3 Flow rate. 0.7 mL/min. 5.3.2.4 Detection cell temperature. 35 C. 5.3.2.5 Column oven temperature. 45 C. 5.3.2.6 Injection volume. 20 L. 5.4 Preparation of Standard Curve Respectively inject the standard series working solutions into the ion chromatograph, determine the corresponding fluoride ion peak height or peak area, and with the fluoride ion concentration of the standard working solution as the horizontal axis and the fluoride ion peak height or peak area as the vertical axis, draw a standard curve. 5.5 Determination of Specimen Solution Inject the specimen solution into the ion chromatograph to obtain the corresponding fluoride ion peak height or peak area. In accordance with the standard curve, obtain the fluoride ion concentration in the specimen solution.

6 Expression of Analytical Results

The fluorine content in the specimen is calculated in accordance with Formula (1).

7 Precision

The absolute difference between two independent determination results obtained under repeatability conditions must not exceed 10% of the arithmetic mean.

8 Others

When the sampling size is 0.5 g (or 1 mL) and the constant volume is 50 mL, the detection limit of the Method is 0.2 mg/kg (or 0.1 mg/L) and the quantification limit is 0.5 mg/kg (or 0.25 mg/L).

9 Principle

The fluoride in the specimen is extracted with water and determined with a fluoride ion selective electrode under a certain total ionic strength.

10 Reagents and Materials

Unless otherwise specified, all reagents used in this Method are analytically pure, the water is Grade-3 water specified in GB/T 6682, and all utensils used are made of plastic (polyethylene or polypropylene). 10.1 Reagents 10.2 Preparation of Reagents 10.2.1 Sodium acetate solution (3 mol/L). weigh-take 204 g of sodium acetate and dissolve it in 300 mL of water. Add acetic acid (1 mol/L) to adjust the pH to 7.0 and add water to a constant volume of 500 mL. 10.3 Standard Substance Same as 3.3. 10.4 Preparation of Standard Solutions 10.4.1 Fluoride standard stock solution (1,000 mg/L). see 3.4.1. 10.4.2 Fluorine standard intermediate solution (50.0 mg/L). accurately transfer-take 5.00 mL of fluorine standard stock solution (1,000 mg/L) into a 100 mL volumetric flask, add water to reach a constant volume and mix it well. At 0 C ~4 C, store it sealed and away from light, and it shall remain valid for 2 months. ......
Source: Above contents are excerpted from the full-copy PDF -- translated/reviewed by: www.ChineseStandard.net / Wayne Zheng et al.


      

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