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GB 1258-2008 English PDF

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GB 1258-2008: Working chemical -- Potassium iodate
Status: Valid

GB 1258: Historical versions

Standard IDUSDBUY PDFLead-DaysStandard Title (Description)Status
GB 1258-2008169 Add to Cart 3 days Working chemical -- Potassium iodate Valid
GB 1258-1990239 Add to Cart 2 days Working chemical--Potassium iodate Obsolete

Similar standards

HG/T 3489   GB/T 1282   HG/T 3484   GB 1260   GB 6853   GB 1256   

Basic data

Standard ID: GB 1258-2008 (GB1258-2008)
Description (Translated English): Working chemical -- Potassium iodate
Sector / Industry: National Standard
Classification of Chinese Standard: G61
Classification of International Standard: 71.040.30
Word Count Estimation: 7,783
Date of Issue: 2008-06-18
Date of Implementation: 2009-06-01
Older Standard (superseded by this standard): GB 1258-1990
Regulation (derived from): Announcement of Newly Approved National Standards No. 10 of 2008 (total 123)
Issuing agency(ies): General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China, Standardization Administration of the People's Republic of China
Summary: This Chinese standard specifies the Working chemical properties of potassium iodate, specifications, testing, inspection and marking and packaging rules. This standard applies to Working chemical titration with potassium iodate test.

GB 1258-2008: Working chemical -- Potassium iodate

---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.
Working chemical.Potassium iodate ICS 71.040.30 G61 National Standards of People's Republic of China Replacing GB 1258-1990 Working Standard reagent potassium iodate Posted 2008-06-18 2009-06-01 implementation Administration of Quality Supervision, Inspection and Quarantine of People's Republic of China Standardization Administration of China released

Foreword

The standard Chapter 4, 5.2.1 and 5.2.2 are mandatory, other provisions are recommended. This standard replaces GB 1258-1990 "work reference reagent (capacity) of potassium iodate," compared with GB 1258-1990, major changes as follows. --- Standard name to "work reference reagent potassium iodate"; --- Modify the Content Measurement (1990 version 4.1, this version 5.3). The standard proposed by China Petroleum and Chemical Industry Association. This standard by the National Standardization Technical Committee Chemistry Chemicals Branch (SAC/TC63/SC3) centralized. This standard is drafted by. Beijing Institute of chemical reagents. The main drafters of this standard. Han Baoying, strong Jing Lin. This standard replaces the standards previously issued as follows. --- GB 1258-1977, GB 1258-1990. Working Standard reagent potassium iodate Warning. some of the test procedure specified in this standard can lead to dangerous situations, the user has the responsibility to take appropriate safety and health practices. Molecular formula. KIO3 Molecular weight. 214.00 (according to 2005 international relative atomic mass).

1 Scope

This standard specifies the reference reagent potassium iodate work traits, specifications, testing, packaging and inspection rules and signs. This standard applies to titration analysis work reference reagent potassium iodate test.

2 Normative references

The following documents contain provisions which, through reference in this standard and become the standard terms. For dated references, subsequent Amendments (not including errata content) or revisions do not apply to this standard, however, encourage the parties to the agreement are based on research Whether the latest versions of these documents. For undated reference documents, the latest versions apply to this standard. Preparation of GB/T 601 chemical reagent standard titration solution GB/T 602 Determination of impurities in chemical reagents prepared standard solution (GB/T 602-2002, ISO 6353-1. 1982, NEQ) with GB/T 603 chemical reagent test method Preparations of articles (GB/T 603-2002, ISO 6353-1 with. 1982, NEQ) GB/T 609 chemical reagent - General method for determination of total nitrogen (GB/T 609-2006, ISO 6353-1. 1982, NEQ) GB/T 6682 analytical laboratory use specifications and test methods (GB/T 6682-2008, ISO 3696. 1987, MOD) GB/T 9724 General rule for determination of pH chemical reagent (GB/T 9724-2007, ISO 6353-1. 1982, NEQ) GB/T 9728 General method for determination of chemical reagents sulfate (GB/T 9728-2007, ISO 6353-1. 1982, NEQ) GB/T 9739 General method for determination of iron chemical reagents (GB/T 9739-2006, ISO 6353-1. 1982, NEQ) Determination of working reference reagent content GB 10737 General Weighing potentiometric titration GB 15258 rules for preparation of chemical safety labels GB 15346 chemical reagent packaging and marking HG/T 3484 standard chemical reagents glass emulsion and clarity standards HG/T 3921 Chemicals sampling and acceptance rules

3 Characters

This reagent is a white crystalline powder, soluble in water, soluble in ethanol.

4 Specification

Potassium iodate as shown in Table 1. Table 1 Name reference work Content (KIO3), /% 99.95 ~ 100.05 pH value (50g/L, 25 ℃) 5.0 ~ 8.0 Clarity test, number ≤2 Table 1 (continued) Name reference work Loss on drying, /% ≤0.1 Chloride and chlorate (as Cl dollars), /% ≤0.005 Iodide (I), /% ≤0.001 Sulphate (SO4), /% ≤0.003 Total nitrogen (N), /% ≤0.002 Iron (Fe), /% ≤0.0002 Heavy metals (Pb), /% ≤0.0005

5 Test

5.1 General provisions Unless specified otherwise in this chapter, the use of standard titration solution, standard solution, preparations and products, according to GB/T 601, GB/T 602, Regulations preparation, test water should be consistent with GB/T 6682 specifications in three water samples according to precise weighing 0.01g, the use of GB/T 603's Solution "%" are represented by the mass fraction. 5.2 Content Measured according to the provisions of GB 10737. 5.2.1 standard titration with sodium thiosulfate solution titration standard potassium iodate Weigh 0.1g has 180 ℃ ± 2 ℃ constant weight standard substance potassium iodate, accurate to 0.00001g, placed in a reaction flask, is dissolved 25mL water, add 3g of potassium iodide and 5mL hydrochloric acid solution (20%), shaken, placed in the dark for 10min, add 150mL water (not to exceed 10 ℃), with 213 platinum electrode as the indicator electrode with a 212-type saturated calomel electrode as reference electrode, according to the provisions of GB 10737, with thiosulfate Sulfate standard titration solution [Ba (NaS2O3) = 0.1mol/L] titrated to the end point. Weighing sodium thiosulfate standard titration solution, to be precise 0.0001g. Determination 5.2.2 Content 5.2.1 Determination of the same, with the measurement sample instead of the standard material loss after drying. The mass fraction of potassium iodate, the value in the "%" means, according to equation (1). (1) Where. B --- material content standard potassium iodate (mass fraction), the value to "%" means; Measured according to the provisions of GB 9724. 5.4 Clarity test Clarity Standard No. 2 Weigh 5g sample was dissolved in 100mL of water, turbidity is not greater than HG/T 3484 stipulated. 5.5 Loss on drying Weigh 1.5g sample, accurate to 0.0001g, has been placed in the weighing bottle at 180 ℃ ± 2 ℃ constant, the electricity in the 180 ℃ ± 2 ℃ Oven dried to constant weight. Samples retained after drying for constant determination. Loss on drying mass fraction of 1, "%" means, according to equation (2). 100 (2) Where. 5.6 Chloride and chlorate Weigh 1g sample was dissolved in 15mL of warm water, constantly shaking dropwise sulfuric acid (about 20mL) to clarify the solution, heat and cook slowly Boiling, excess sulfur dioxide to escape, cooling, 5mL and 10mL of ammonia water, was added dropwise with stirring 15mL silver nitrate solution (50g/L), Filtered, washed, and the filtrate and washings were combined, diluted to 100mL. Take 20mL, plus 5mL nitric acid solution (25%), shake for 10min. The turbidity of the solution was not greater than the standard turbidity solution. Standard preparation turbid solution is to take the ratio of 0.01mg containing chloride (Cl) standard solution, add 15mL water, 1mL ammonia, 5mL nitric acid Solution (25%) and 1mL silver nitrate solution (50g/L), was diluted to 25mL, and the same volume of test solution placed simultaneously turbidimetric 10min. 5.7 iodide 5g samples were weighed, dissolved in 75mL of water heating, cooling, 0.5mL sulfuric acid solution (20%), extracted with 10mL chloroform, Still stratification. The organic layer is red it can not be deeper than the standard colorimetric solution. Preparation of standard color solution than 0.1g sample is taken and containing 0.05mg iodide (I) standard solution, and treated in the same sample at the same time. 5.8 sulfate Weigh 0.5g sample was added 5mL hydrochloric acid, evaporated on a water bath, add 2mL of hydrochloric acid, and then evaporated to dryness. Repeat process to white residue, residue Residue was dissolved in 15mL of water (filtered if necessary), measured according to GB 9728 regulations. The turbidity of the solution was not greater than the standard turbidity solution. Standard preparation turbid solution is to take the ratio of 0.015mg containing sulfate (SO4) standard solution, and treated in the same sample at the same time. 5.9 total nitrogen content Weigh 1g sample was dissolved in water and diluted to 140mL, determined according to the provisions of GB/T 609's. The yellow solution can not be deeper than the standard ratio Color solution. Preparation of the standard developing solution containing 0.02mg ratio is taken of nitrogen (N) standard solution, the same treatment simultaneously with the sample. 5.10 Iron Weigh 1g sample, add 2 drops of sulfuric acid and hydrochloric acid 10mL, on the steam bath to near dryness, treated with 10mL of hydrochloric acid to the residue was repeatedly changed White, soluble in water (filtered if necessary), diluted to 15mL, with aqueous ammonia solution (10%) and the solution was adjusted to pH 2, according to GB/T 9739 regulations Determination. The red solution should not be deeper than the standard colorimetric solution. Preparation of the standard solution is to take the colorimetric containing 0.002mg of iron (Fe) standard solution, the same treatment simultaneously with the sample. 5.11 Heavy Metal Weigh 4g sample plus 20mL hydrochloric acid, evaporated on a water bath, repeat the process with 10mL of hydrochloric acid to white residue. The residue was dissolved in water, With aqueous ammonia solution (10%) and the solution was adjusted to pH 4, diluted to 40mL, take 30mL, add 0.2mL acetic acid solution (30%) and 10mL Freshly prepared saturated hydrogen sulphide water, shake, place 10min. The solution was dark can not be deeper than the standard colorimetric solution. Preparation of standard color solution is to take over the remaining 10mL test solution containing 0.01mg and lead (Pb) standard solution was diluted to 30mL, and With the same volume of the test solution treated simultaneously.

6 Inspection rules

According to the provisions of HG/T 3921 is sampled and acceptance.

7 Packaging and marking

According to GB 15346 requirements for packaging, storage and transportation, and flags are given, including.
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