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Database: 365,228(8 Aug 2026)
analysis methods calcium oxide chemical analysis potassium oxide sodium oxide standard coal sample acoustics audiometric test methods caramel candy introductionthis standard establishes specifications
GB/T 15343-2012 in English

GB/T 15343-2012 in English

SUPERSEDED

Methods for chemical analysis of talc

  • Issued on:2012-12-31
  • Implemented on:2013-08-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $550.00
$534.00
Standard No: GB/T 15343-2012
Document status: SUPERSEDED
Superseded by: GB/T 15343-2020 Methods for chemical analysis of talc
Superseded on: 2021-04-01
Title in English: Methods for chemical analysis of talc
Title in Chinese: 滑石化学分析方法
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 1~3 business days
Issued on: 2012-12-31
Implemented on: 2013-08-01
Superseding: GB/T 15343-1994 Methods for chemical analysis of talc
ICS Classification: 73.080-Non-metalliferous minerals
Chinese Classification: Q64-Talcum material
Professional Classification: GB-National Standard
Related Keywords: analysis methods
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《GB/T 15343-2012滑石化学分析方法》由609(中国建筑材料联合会)归口,主管部门为中国建筑材料联合会。


1 Scope

This standard specifies the ignition loss of talc product, the content and acidity/alkalinity of silicon dioxide, total iron, aluminum oxide, titanium dioxide, calcium oxide, magnesium oxide, potassium oxide, sodium oxide, hydrochloric acid insoluble substance, acid-soluble iron, acid-soluble calcium, manganese, copper, acid-soluble substance and hydrotrope as well as the analysis methods for chemical constituents like ferric salt, arsenic, heavy metal and lead.
This standard is applicable to the constituent analysis of talc lump and talc powder.

2 Normative References

The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the normative document (including any amendments) applies.
GB/T 8170 Rules of Rounding Off for Numerical Values & Expression and Judgment of Limiting Values
GB/T 15341 Talc Lumps
GB/T 15342 Talc Powder

3 General Provisions

3.1 Except for moisture determination, the specimen shall be dried for 2h under 105~110℃, and then cooled to room temperature in dryer before being weighed.
3.2 Unless otherwise specified, the weighing of specimen shall be accurate to 0.1mg. The constant mass in this method refers to that the difference between 2 weighing is not greater than 0.3mg.
3.3 Unless otherwise specified, only the water recognized as distilled or deionized water or water with equivalent purity is adopted for analysis in this method. All solutions, unless otherwise indicated, refer to water solutions.
3.4 The concentration of solution is the molar concentration or the mass of solute contained in 1L solution (g/L). (1+1), (1+2), (m+n) refer to the ratio of solute volume to water volume.
3.5 Unless otherwise specified, only the reagent recognized as analytical reagent or guaranteed reagent is adopted for analysis, while only the reagent recognized as reference reagent or spectral pure/high-purity reagent is adopted for calibration. Unless otherwise specified, only the acid and ammonia water recognized as concentrated acid or stronger ammonia water are adopted for analysis.
3.6 Except for determination of ignition loss, blank test shall be carried out simultaneously for other determinations, and the determined results shall be calibrated.
3.7 Unless otherwise specified, the value of analysis result (%) shall be rounded off to two decimal places according to GB/T 8170.

4 Specimen

4.1 Sampling
4.1.1 Sampling of talc lump specimen is carried out according to GB/T 15341.
4.1.2 Sampling of talc lump specimen is carried out according to GB/T 15342.
4.2 Specimen Preparation
Pulverize the sample delivered to the laboratory to make it pass through the 1μm sieve; the mass of sample shall not be less than 1kg; reduce the mass to 1000g with quartering or divider; then grind the sample until it completely passes through the 180μm sieve, and reduce the mass to 100g with quartering or divider; regrind the sample until it completely passes through the 75μm sieve, and reduce the mass to 50g with quartering or divider; gather and remove the scrap iron brought by crushed sample with magnet; sufficiently mix it for standby.

Foreword I
1 Scope
2 Normative References
3 General Provisions
4 Specimen
4.1 Sampling
4.2 Specimen Preparation
5 Analysis Methods
5.1 Determination of Ignition Loss
5.2 Determination of Silicon Dioxide
5.3 Determination of Total Iron
5.4 Determination of Aluminium Oxide
5.5 Determination of Titanium Dioxide
5.6 Determination of Magnesium Oxide and Calcium Oxide
5.7 Determination of Potassium Oxide and Sodium Oxide (Flame Photometry)
5.8 Determination of HCl Insoluble
5.9 Determination of Acid-soluble Iron
5.10 Determination of Acid-soluble Calcium
5.11 Determination of Manganese
5.12 Determination of Copper
5.13 Determination of Acid-soluble Substance
5.14 Determination of Hydrotrope and Acid-base Property
5.15 Determination of Ferric Salt
5.16 Determination of Arsenic
5.17 Determination of Heavy Metals
5.18 Determination of Lead
5.19 Determination of Potassium Oxide, Sodium Oxide, Calcium Oxide and Total Iron (Atomic Absorption Spectrometry)

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