GB 1886.62-2015 English PDF

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GB 1886.62-2015: National Food Safety Standard -- Food Additives -- Magnesium silicate
Status: Valid

Standard ID	USD	BUY PDF	Lead-Days	Standard Title (Description)	Status
GB 1886.62-2015	169	Add to Cart	3 days	National Food Safety Standard -- Food Additives -- Magnesium silicate	Valid

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Basic data

Standard ID: GB 1886.62-2015 (GB1886.62-2015)
Description (Translated English): National Food Safety Standard -- Food Additives -- Magnesium silicate
Sector / Industry: National Standard
Classification of Chinese Standard: X09
Word Count Estimation: 8,856
Date of Issue: 2015-09-22
Date of Implementation: 2016-03-22
Regulation (derived from): PRC National Health and Family Planning Commission 2015 No.8
Issuing agency(ies): National Health and Family Planning Commission of the People's Republic of China
Summary: This standard applies to sodium silicate and soluble magnesium salt by precipitation reaction of food additives produced magnesium silicate.

GB 1886.62-2015: National Food Safety Standard -- Food Additives -- Magnesium silicate

---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 magnesium silicate) National Standards of People's Republic of China National Food Safety Standard Food additive magnesium silicate Issued on. 2015-09-22 2016-03-22 implementation People's Republic of China National Health and Family Planning Commission released National Food Safety Standard Food additive magnesium silicate

1 Scope

This standard applies to the soluble sodium and magnesium salts precipitated the reaction of a food additive magnesium silicate.

2 Technical Requirements

2.1 Sensory requirements Sensory requirements shall comply with the requirements of Table 1. Table 1 Sensory requirements Project requires test methods Color White State powder Take the right amount of sample is placed in white porcelain dish, viewed in natural light Its color and status 2.2 Physical indicators Physical and chemical indicators should be consistent with the provisions of Table 2. Table 2. Physical and chemical indicators Item Index Test Method Magnesium oxide (MgO, with burning base count), w /% ≥ 15.0 Appendix A A.3 Silica (SiO2, with burning base count), w /% ≥ 67.0 Appendix A A.4 Loss on drying, w /% in line with GB 5009.3 claiming a direct drying Loss on ignition (dry basis), w /% in line with claims A.5 in Appendix A Soluble salts, w /% ≤ 3.0 A.6 in Appendix A The free base (NaOH in dollars), w /% ≤ 1.0 Appendix A A.7 Fluoride/(mg/kg) ≤ 10 Appendix A A.8 Lead (Pb)/(mg/kg) ≤ 5.0 GB 5009.75 a drying temperature of 105 ℃ ± 2 ℃, drying time is 2h.

Appendix A

Testing method A.1 General Provisions Unless otherwise specified in this standard, the use of reagents were of analytical grade purity, the standard titration solution, impurity measurement standard solution preparation And products, should be GB/T 601, GB/T 602 and GB/T 603 provisions of preparation, the test water should comply with GB/T 6682 in three water Provisions. Solution was used in the tests did not indicate what is formulated with solvent, it refers to an aqueous solution. A.2 Identification Test A.2.1 pH test Weighed amount of sample preparation with water to 100g/L slurry solution, pH 7.0 to 11.0. A.2.2 Identification of magnesium A.2.2.1 Reagents and materials A.2.2.1.1 hydrochloric acid solution. 19. A.2.2.1.2 ammonia solution. 19. A.2.2.1.3 ammonium carbonate solution. 20g of ammonium carbonate dissolved in ammonia solution 20mL, diluted with water to 100mL. A.2.2.1.4 sodium phosphate. disodium hydrogen phosphate (NaH2PO4 · 7H2O) were dissolved in water to prepare a solution of 120g L /. A.2.2.2 Identification of Weigh a sample of about 0.5g, and hydrochloric acid mixed solution of 10mL, filtered, and the filtrate was collected. With ammonia solution and filtrate to litmus paper Neutral solution of ammonium carbonate was added 5mL, stir, this time should not precipitate. 5mL was added a solution of sodium phosphate, were observed as white The precipitate crystals, 10mL aqueous ammonia solution was added, a white insoluble precipitate crystals. Identification A.2.3 silicate Platinum wire ring dipped in sodium ammonium phosphate crystallization number of tablets, pellets melted after the colorless flame, hot dipped in the sample, and then melted silica i.e. Floating on the surface of the ball, let cool, reticular structure opaque pellets. A.3 Determination of magnesium oxide (MgO, with burning basis) of A.3.1 Reagents and materials A.3.1.1 sulfuric acid standard titration solution. c 12H2SO4 ÷ = 1mol/L. A.3.1.2 sodium hydroxide standard titration solution. c (NaOH) = 1mol/L. A.3.1.3 methyl orange indicator solution. 1g/L. A.3.2 Analysis step Weigh a sample of about 1.5g, accurate to 0.0001g, placed in 250mL Erlenmeyer flask with a pipette 50.0mL sulfuric acid standard titration The solution was heated on a steam bath for 1h, cooled to room temperature, add a few drops of methyl orange indicator solution, titration with sodium hydroxide standard solution titration of excess Acid, titrated to a solution from red to orange, 30s without recovery is the primary endpoint of the titration. A.3.3 Calculation Results Magnesium oxide (MgO, with burning basis) mass fraction w1, according to equation (A.1) Calculated. w1 = (V0 × c0-V × c) × M m × (1-w0) × (1-w3) × 1000 × 2 × 100% (A.1) Where. V0 --- volume of sulfuric acid standard titration solution (V0 = 50), in milliliters (mL); Concentration c0 --- sulfuric acid standard titration solution, expressed in moles per liter (mol/L); Volume V --- sample consumption of sodium hydroxide standard titration solution, in milliliters (mL); C --- concentration of sodium hydroxide standard titration solution, expressed in moles per liter (mol/L); --- The M molar mass of magnesium oxide in grams per mole (g/mol), [M (MgO) = 40.3]; M --- the quality of the sample, in grams (g); w0 --- Loss on drying of the sample mass fraction,%; w3 --- sample mass fraction of loss on ignition,%; 1000 --- volume conversion factor; 2 --- molar conversion coefficient. 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 1.0%. A.4 silicon dioxide (SiO2, with burning basis) Determination A.4.1 Reagents and materials A.4.1.1 hydrofluoric acid. A.4.1.2 sulfuric acid. A.4.1.3 sulfuric acid solution. c 12H2SO4 ÷ = 1mol/L. A.4.2 Instruments and Equipment A.4.2.1 platinum crucible. 50mL. A.4.2.2 high-temperature furnace. temperature can be controlled to 900 ℃ ± 50 ℃. A.4.3 Analysis step Weigh the sample 0.7g, accurate to 0.0001g, placed in a 150mL beaker, pipetted into 20mL sulfuric acid solution in distilled Gas heating bath on 1.5h, filter ash-free filter paper. With about 100mL60 ℃ ~ 80 ℃ hot water residue was washed three times. The filter paper and a residue Shall be transferred to a platinum crucible in an electric furnace heated slowly drying, ashing, and then on the 900 ℃ high temperature furnace burning strong 30min, after cooling, said Weight (m1). The residue was moistened with water, and add 3 drops of sulfuric acid and hydrofluoric acid 6mL, on a hot plate was slowly evaporated to dryness at 900 ℃ high temperature furnace on Burning 5min, cooled, weighed (m2). SiO2 were weighed twice difference is quality. A.4.4 Calculation Results Silica (SiO2, with burning basis) mass fraction w2, according to equation (A.2) Calculated. w2 = m1-m2 m × (1-w0) × (1-w3) × 100% (A.2) Where. After m1 --- burning crucible together with residue mass in grams (g); After m2 --- acid residue burning crucible together with the mass in grams (g); M --- the quality of the sample, in grams (g); w0 --- Loss on drying of the sample mass fraction,%; w3 --- sample mass fraction of loss on ignition,%. 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 1.0%. A.5 Determination of loss on ignition (dry basis) of A.5.1 Analysis step The sample was dried reduction assay reserved in a hot oven at 900 ℃ ~ 1000 ℃ burning 20min. A.5.2 Calculation Results Loss on ignition (dry basis) of the mass fraction w3, according to equation (A.3) Calculated. w3 = m3-m4 m × 100% (A.3) Where. M3 --- Loss on drying specimens retained along with the determination of the total mass of the crucible, in grams (g); m4 --- Residue on ignition crucible together with mass, in grams (g); Determination of mass m --- Loss on drying retained sample in grams (g). 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 0.5%. A.6 Determination of soluble salts A.6.1 Preparation of sample solution Weigh 10g sample, accurate to 0.01g, placed in a beaker, was added 150mL of water on a hot plate heated to boiling 15min. Cooled to room Temperature, add water to make up to the original volume. The mixture was allowed to stand for 15min, the filtrate was filtered to clarification. The filtrate 20mL reserved for the free base Determination. A.6.2 Determination Take 75mL sample solution was added 25mL of water and shake. 50mL take the mixed solution (equivalent to 2.5g sample), was placed in a constant weight Crucible, evaporated to dryness on a steam bath and then calcined in an electric furnace and then slowly to constant weight. The quality of the residue should not exceed 75mg, that is soluble The salt content of not more than 3.0%. A.7 Determination of the free base (with NaOH basis) A.7.1 Reagents and materials A.7.1.1 hydrochloric acid standard titration solution. c (HCl) = 0.1mol/L. A.7.1.2 phenolphthalein indicator solution. 10g/L. A.7.2 Analysis step Take 20mL sample solution (A.6.1.) (Equivalent to 1g sample), 2 drops of phenolphthalein indicator solution. If pink, then with hydrochloric acid Standard Volumetric titration to a colorless solution, hydrochloric acid standard titration solution consumed should not exceed 2.5mL, namely the free base (NaOH in dollars) of quality Volume fraction of less than 1%. A.8 Determination of fluoride A.8.1 Reagents and materials A.8.1.1 disodium edetate. A.8.1.2 Tris. A.8.1.3 sodium fluoride. A.8.1.4 sodium hydroxide solution. 5mol/L. A.8.1.5 hydrochloric acid solution. 1mol/L. A.8.1.6 Water. GB/T 6682-2008 in two water regulations. A.8.2 Instruments and Equipment A.8.2.1 Potentiometer. accuracy of ± 0.2mV. A.8.2.2 electrodes. indicator electrode is a suitable fluoride ion selective electrode; a reference electrode is a saturated calomel electrode. A.8.2.3 beaker. polytetrafluoroethylene material. A.8.3 Analysis step A.8.3.1 Disodium edetate - Preparation of Tris solution The disodium edetate and 18.6g 6.05g Tris placed in a 250mL beaker was added 200mL hot Water and stirred until dissolved. The solution was adjusted with 5mol/L sodium hydroxide solution to pH 7.5 to 7.6, cooled, treated with 5mol/L sodium hydroxide solution The solution was adjusted to pH 8.0. The solution was transferred to 250mL volumetric flask, dilute with water to volume, mix and stored in plastic containers. A.8.3.2 Preparation of standard stock solution Weigh 2.210g sodium fluoride, dissolved in 50mL water. The solution is transferred to 1000mL volumetric flask, dilute with water to volume, and mix, as A concentrated standard solution. Draw this solution 10mL, placed in 100mL volumetric flask, dilute to the mark with water, mix, diluting as standard Stock solution. Final dilution of stock standard solution of fluoride concentration of 100mg/kg. Note. All concentrated and diluted fluoride standard solution should be stored in plastic containers. This standard solution and sample solution should be in the following day of use preparation. A.8.3.3 Preparation of standard solutions Draw stock standard solution 10mL and 1mL, were placed in 100mL flask, diluted with water to the mark. Two standard solutions stars Do fluorine 10mg/kg and 1mg/kg. A.8.3.4 Preparation of sample solution The 5.0g sample is placed in 150mL beaker, add 40mL of water and 20mL hydrochloric acid solution under constant stirring and heated to a boil 1min. In an ice bath to cool, transferred to a 100mL volumetric flask, diluted with water to the mark. After standing the supernatant as a sample solution. A.8.3.5 Drawing standard curve Draw two standard solution of 20mL, 100mL were placed in a beaker. EDTA was added 10mL in each beaker Disodium - Tris solution. Potentiometric measuring device (potentiometer connected to the electrode) were measured potential of the standard solution. To refer to It shows electrode potential (mV) for the vertical axis, with the fluoride ion concentration (mg/kg) as the abscissa, the standard curve. A.8.3.6 Determination 20mL draw sample solution, placed in 100mL beaker, disodium edetate was added 10mL - Tris solution Solution, the sample solution potential (mV) and measured according to the method described in A.8.3.5. Against a standard curve by the sample solution measured electrical Bit computing a fluoride content (mg/kg). 5102- 26􀏕 6881 ......

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