GB 1886.8-2015 English PDF

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GB 1886.8-2015: National Food Safety Standards -- Food additives -- Sodium sulfite
Status: Valid

Standard ID	USD	BUY PDF	Lead-Days	Standard Title (Description)	Status
GB 1886.8-2015	169	Add to Cart	3 days	National Food Safety Standards -- Food additives -- Sodium sulfite	Valid

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Basic data

Standard ID: GB 1886.8-2015 (GB1886.8-2015)
Description (Translated English): National Food Safety Standards -- Food additives -- Sodium sulfite
Sector / Industry: National Standard
Classification of Chinese Standard: X42
Word Count Estimation: 8,810
Date of Issue: 2015-11-13
Date of Implementation: 2016-05-13
Older Standard (superseded by this standard): GB 1894-2005
Regulation (derived from): National Health and Family Planning Commission Announcement No
Issuing agency(ies): National Health and Family Planning Commission of the People's Republic of China

GB 1886.8-2015: National Food Safety Standards -- Food additives -- Sodium sulfite

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
(National food safety standards for food additives sodium sulfite) National Standards of People's Republic of China National Food Safety Standard Food additive sodium sulfite Issued on. 2015-11-13 2016-05-13 implementation People's Republic of China National Health and Family Planning Commission released

Foreword

This standard replaces GB 1894-2005 "food additive anhydrous sodium sulphite." This standard compared with GB 1894-2005, the main changes are as follows. --- Standard name was changed to "national food safety standards for food additives sodium sulfite." National Food Safety Standard Food additive sodium sulfite

1 Scope

This standard applies to food additive sodium sulfite.

2 molecular formula and relative molecular mass

Formula 2.1 Na2SO3 2.2 relative molecular mass 126.05 (according to 2007 international relative atomic mass)

3 Technical requirements

3.1 Sensory requirements Sensory requirements shall comply with the requirements of Table 1. Table 1 Sensory requirements Project requires test methods Color White Status crystalline powder Take the right amount of sample is placed in 50mL beaker was observed under natural light Color and status 3.2 Physical and Chemical Indicators Physical and chemical indicators should be consistent with the provisions of Table 2. Table 2. Physical and chemical indicators Item Index Test Method Sodium sulfite (Na2SO3) content (dry basis), w /% ≥ 96.0 Appendix A A.4 Iron (Fe), w /% ≤ 0.01 Appendix A A.5 The free base (in Na2CO3 dollars), w /% ≤ 0.60 A.6 in Appendix A Heavy metals (Pb)/(mg/kg) ≤ 10.0 GB 5009.74 Arsenic (As)/(mg/kg) ≤ 2.0 GB 5009.76 Clarity through test A.7 in Appendix A

Appendix A

Testing method A.1 Warning Reagents The test method used in toxic or corrosive, the operator should be careful. Such as water splashed on the skin should immediately Flushing, severe cases should be treated immediately. When using flammable, do not use open flame heating. A.2 General Provisions This standard reagents and water, did not indicate when the other requirements, refer to analytical reagent and third grade water GB/T 6682 regulations. Standard solutions used in the tests, impurity standard solution, preparations and products, did not indicate when the other requirements, according to GB/T 601, GB/T 602 And the provisions of GB/T 603 formulation. Solution was used in the tests did not indicate what is formulated with solvent, it refers to an aqueous solution. A.3 Identification Test A.3.1 Reagents and materials A.3.1.1 hydrochloric acid solution. 13. A.3.1.2 iodine solution (14g/L). Weigh 1.4g iodine dissolved 10mL360g/L potassium iodide solution, add 1 drop to 2 drops of hydrochloric acid, water Diluted to 100mL, stored in a brown bottle in the dark save. A.3.1.3 mercurous nitrate solution (150g/L). Weigh 15g mercurous nitrate, dissolved in 90mL water and 10mL nitric acid solution (19), the drop Add 1 drop of mercury, dark sealed. A.3.2 Identification method A.3.2.1 preparation of the sample solution Weigh 20.0g ± 0.1g sample was dissolved in 100mL of water, Extemporaneous. A.3.2.2 Identification sulfite A.3.2.2.1 test sample solution with pH paper, pH of about 9. A.3.2.2.2 Take 5mL sample solution is placed in a test tube, drip iodine solution, yellow fade. A.3.2.2.3 Take 5mL sample solution is placed in a test tube, drip hydrochloric acid, sulfur dioxide gas to escape. Mercurous nitrate wetted The filter paper test was black. A.3.2.3 Identification of sodium ions Hydrochloric acid infiltration of platinum wire in the first combustion flame colorless to colorless, then dipped a little in the sample solution is colorless combustion flame, the flame was bright yellow. A.4 Determination of sodium sulfite (Na2SO3) content (dry basis) of A.4.1 Method summary In weak acid solution, adding a certain excess iodine oxidation of sulfite. Starch as indicator, with an excess of sodium thiosulfate solution titrated Iodine. A.4.2 Reagents and materials A.4.2.1 hydrochloric acid solution. 11. A.4.2.2 iodine solution. c ( 2I2 ) = 0.1mol/L. A.4.2.3 sodium thiosulfate standard titration solution. c (Na2S2O3) = 0.1mol/L. A.4.2.4 starch indicator solution. 5g/L, use a period of two weeks. A.4.3 Analysis step Quickly weighed about 0.2g sample (accurate to 0.0002g), placed in a pre burette added 40.00mL iodine solution and 30mL ~ 50mL water 250mL iodine bottle, add 2mL hydrochloric acid solution, and immediately cover the cork, seal, after shaking slowly dissolve into the dark place Set 5min. When titrated with sodium thiosulfate standard solution titration to pale yellow solution, adding about 3mL starch indicator solution and continue titration to Blue is the end disappear. Make a blank test simultaneously. In addition to the blank test without the sample, the addition of reagents and other operations of the kind and amount (other than the standard titration solution) with the same Test. A.4.4 Calculation Results Sodium sulfite (Na2SO3) content (dry basis) w1, according to formula (A.1) Calculated. w1 = (V1-V2) × c1 × M1 m1 × 1000 × 100% (A.1) Where. Volume of sodium thiosulfate standard titration V1 --- titrate blank solution consumed solution in milliliters (mL); Volume of sodium thiosulfate standard titration V2 --- titration solution consumed by the sample solution, in milliliters (mL); Concentration c1 --- sodium thiosulfate standard titration solution, expressed in moles per liter (mol/L); --- Sodium sulfite molar mass Ml of units of grams per mole (g/mol), [M1 ( 2Na2SO3 ) = 63.02]; M1 --- the quality of the sample, in grams (g); 1000 --- conversion factor. The results parallel arithmetic mean of the measurement results shall prevail. Twice under the same condition of independent determination results obtained absolute difference Not more than 0.3%. A.5 Determination of iron (Fe) of A.5.1 Method summary Reduction with ascorbic acid in the sample solution of ferric ions into ferrous ions, at a pH of from 2 to 9.00, a divalent iron ions with phenanthroline Morpholino generated orange-red complex with a spectrophotometer measuring the absorbance at the maximum absorption wavelength at 510nm. A.5.2 Reagents and materials GB/T 3049-2006 in accordance with Chapter 4. A.5.3 Instruments and Equipment GB/T 3049-2006 in accordance with Chapter 5. A.5.4 Analysis step A.5.4.1 draw the curve GB T 3049-2006 according to the provisions of 6.3/use of 4cm or 5cm iron absorption cell and the corresponding standard solution, drawn work curve. A.5.4.2 Preparation of sample solution Weigh about 1g sample (accurate to 0.01g), placed in 150mL beaker, dissolved in 10mL water, was added 5mL of hydrochloric acid, in a water bath On evaporated to dryness. After the residue was dissolved in water, all transferred to 100mL volumetric flask and set aside. A.5.4.3 Preparation of blank solution Except that no sample addition, the same amount of reagent preparation to join the other with the sample solution and simultaneously. A.5.4.4 sample measurement In the flask containing the sample solution and the blank solution, add water to 60mL, with ammonia solution or hydrochloric acid solution to adjust the pH to 2, with fine Dense dipstick test pH. The test solution quantitatively transferred to 100mL volumetric flask, add 1mL ascorbic acid solution, then add 20mL buffer 10mL1,10- phenanthroline solution and the solution diluted with water to the mark. For not less than 15min. Determination of two test solution absorbance. A.5.4.1 selection and specification in the same absorption cell (4cm or 5cm absorption cell), according to GB/T 3049-2006 measured as specified in 6.4 Absorbance, find out the quality of the sample solution and blank solution of iron from the working curve. A.5.5 Calculation Results Iron (Fe) mass fraction w2, according to equation (A.2) Calculated. w2 = m2-m3 m4 × 1000 × 100% (A.2) Where. m2 --- Richard from the working curve of the sample solution in iron mass, in milligrams (mg); m3 --- Richard from the working curve of the blank solution iron mass, in milligrams (mg); M4 --- the quality of the sample, in grams (g); 1000 --- conversion factor. The results parallel arithmetic mean of the measurement results shall prevail. Twice under the same condition of independent determination results obtained absolute difference Not more than 0.0005%. A.6 Determination of the free base (in Na2CO3 basis) A.6.1 Method summary Sample addition of hydrogen peroxide, sulfite oxidation, titration with hydrochloric acid standard solution titration sample of the free base. A.6.2 Reagents and materials A.6.2.1 hydrogen peroxide solution. mass fraction of 20%. Methyl red indicator solution with sodium hydroxide solution [c (NaOH) = 0.1mol/L] neutralize. A.6.2.2 hydrochloric acid standard titration solution. c (HCl) = 0.1mol/L. A.6.2.3 methyl red indicator solution. 1g/L. A.6.3 Instruments and Equipment Microburette. indexing is 0.02mL. A.6.4 Analysis step Weigh about 2g sample (accurate to 0.01g), placed in 250mL conical flask, dissolved in 20mL of water was added 5mL of hydrogen peroxide solution Liquid, shake. In the water bath solution was evaporated to about 1/2 of its original volume, cooling, 10mL of water was added, dropping 1 drop of methyl red indicator solution, so that Using a micro burette, titrate with hydrochloric acid standard titration solution until the solution changed from yellow to red is the end. A.6.5 Calculation Results The free base (in Na2CO3 meter) mass fraction w3, according to equation (A.3) Calculated. w3 = V3 × c2 × M2 m5 × 1000 × 100% (A.3) Where. Volume V3 --- hydrochloric acid standard titration solution consumed in the titration sample solution, in milliliters (mL); c2 --- hydrochloric acid standard titration solution concentration, in units of moles per liter (mol/L); The M2 --- sodium carbonate molar mass in grams per mole (g/mol), [M2 ( 2Na2CO3 ) = 52.99]; M5 --- the quality of the sample, in grams (g); 1000 --- conversion factor. The results parallel arithmetic mean of the measurement results shall prevail. Twice under the same condition of independent determination results obtained absolute difference Not more than 0.02%. Determination A.7 of clarity A.7.1 Reagents and materials A.7.1.1 nitric acid solution. 13. A.7.1.2 silver nitrate solution. 20g/L. A.7.1.3 dextrin solution. 20g/L. A.7.1.4 chloride standard solution. 1mL solution containing chlorine (Cl) 0.01mg, Extemporaneous. Pipette pipette 10mL chloride Standard solution, placed in 100mL flask, diluted with water to the mark. A.7.2 Analysis step A.7.2.1 turbidity standard solution preparation Pipette Pipette 0.5mL chloride standard solution, placed in 25mL colorimetric tube, add water to about 20mL, nitric acid solution is added 1mL Solution, 0.2mL dextrin solution, 1mL nitrate solution, add water to the mark, shake, place 15min sunshine at avoiding direct. A.7.2.2 turbidity comparison Weigh 1.25g ± 0.01g sample was placed in 100mL beaker, all dissolved in water transferred to 25mL colorimetric tube, add water to the mark Degree, shake, is the sample solution. The comparison with the standard sample solution turbidity solution, avoid direct sunlight, when viewed from above and the side, the sample Turbidity of the solution is not more than the standard shown nephelometric turbidity of the solution, the solution could barely see the floats and other foreign substances, namely through tests. ......

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