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GB/T 23274.3-2009Methods for chemical analysis of stannic oxide - Part 3: Determination of arsenic content - Molybdoantimonyarsenate blue spectrophotometric method (English PDF)

二氧化锡化学分析方法 第3部分:砷量的测定 砷锑钼蓝分光光度法

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Issued by

SAMR; SAC

Level / Type

National · Recommended

Issue date

January 5, 2009

Implementation date

November 1, 2009

Scope

GB/T 23274.3-2009 is the English-translated version of 二氧化锡化学分析方法 第3部分:砷量的测定 砷锑钼蓝分光光度法.

GB/T 23274.3-2009 is the Chinese standard "Methods for chemical analysis of stannic oxide - Part 3: Determination of arsenic content - Molybdoantimonyarsenate blue spectrophotometric method".

Its scope clause reads: This section GB/T 23274 specifies the determination of arsenic content of tin dioxide. This section applies to the determination of arsenic content in tin dioxide, measured in the range of 0.00020% to 0.050%. Its clauses include method summary; reagents and apparatus.

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Document preview — GB/T 23274.3-2009

National Standard of the People's Republic of China

ICS
71.040.40
Classification
G 10

Issued by: State Administration for Market Regulation; Standardization Administration of the PRC

Contents

  • 1 Scope
  • 2 Method summary
  • 3 Reagents and apparatus
  • 3.9 stannous chloride solution (400g/L)
  • 3.10 absorption solution (2g/L)
  • 3.11 ascorbic acid solution (30g/L)
  • 3.14 color solution
  • 3.15 arsenic standard stock solution
  • 3.16 Arsenic standard solution
  • 3.17 arsine occurred and absorption devices

1 Scope

This section GB/T 23274 specifies the determination of arsenic content of tin dioxide.

This section applies to the determination of arsenic content in tin dioxide, measured in the range of 0.00020% to 0.050%.

2 Method summary

The sample is dissolved in water, dilute sulfuric acid medium with stannous chloride, zinc metal arsenic is reduced to arsine gas, arsenic and antimony, molybdenum generate blue

Antimony molybdenum blue, the absorbance is measured in a spectrophotometer at a wavelength of 700nm.

3 Reagents and apparatus

Test water are a distilled water.

3.1

arsenic-free zinc particles (u00d83mm ~ u00d87mm).

3.2

potassium chlorate.

3.3

sulfate (rho1.84g/mL).

3.4

sulfate (1 + 1).

3.5

sulfate (1 + 6).

3.6

hydrochloride (rho1.19g/mL).

3.7

HCl (1 + 1).

3.8

tartaric acid solution (300g/L).

3.9 stannous chloride solution (400g/L)

Weigh 40g of stannous chloride (SnCl2 · 2H2O) in 200mL beaker, add 80mL hydrochloric acid (3.6), cover the dish table, micro heat of solution is completely clear, and cooled to room temperature, hydrochloric acid (3.7) diluted to 100mL, and mix.

3.10 absorption solution (2g/L)

Weigh 1g and 5g potassium iodine tablets mixed, dissolved in water and diluted to 500mL.

3.11 ascorbic acid solution (30g/L)

now with the current.

3.12

ammonium molybdate solution (40g/L).

3.13

antimony potassium tartrate solution (4.5g/L).

3.14 color solution

Take 50mL sulfuric acid (3.5), 25mL ascorbic acid solution (3.11), 20mL ammonium molybdate solution (3.12), 5mL

Antimony potassium tartrate solution (3.13) and mix. The time is now equipped with.

3.15 arsenic standard stock solution

Weigh 0.1320g trioxide (reference reagent, pre-drying to a constant weight at 105 °C ± 5 °C), put

150mL beaker, 10mL sodium hydroxide solution (200g/L) dissolved, 5mL of sulfuric acid (3.3), 0.5mL of hydrogen peroxide (30%),

Heated to boiling for 10min, cooled to room temperature. Moved into 1000mL volumetric flask, dilute with water to volume, and mix. This solution containing 1mL

100µg arsenic.

3.16 Arsenic standard solution

Pipette 25.00mL arsenic standard stock solution (3.15), placed in 500mL volumetric flask, dilute to the mark,

Mix well. This solution 1mL containing 5µg arsenic.

3.17 arsine occurred and absorption devices

Arsine occurred and absorbing device shown in Figure 1.

......
This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 15 pages — is available in the English PDF.

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