GB/T 11213.2-2007 PDF English (GB/T 11213.2-1989: Older version)
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Sodium hydroxide for chemical fiber use - Determination of sodium chloride content - Spectrometric method
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| GB/T 11213.2-1989 | English | 199 |
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Sodium hydroxide for chemical fiber use--Determination of sodium chloride content--Spectrometric method
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GB/T 11213.2-2007: PDF in English (GBT 11213.2-2007) GB/T 11213.2-2007
GB
NATIONAL STANDARD OF THE
PEOPLE’S REPUBLIC OF CHINA
ICS 71.060.40
G 11
Replacing GB/T 11213.2-1989
Sodium Hydroxide for Chemical Fiber Use – Determination
of Sodium Chloride Content – Spectrometric Method
ISSUED ON: AUGUST 13, 2007
IMPLEMENTED ON: FEBRUARY 01, 2008
Issued by: General Administration of Quality Supervision, Inspection and
Quarantine;
Standardization Administration of the People’s Republic of China.
Table of Contents
Foreword ... 3
1 Scope ... 5
2 Normative References ... 5
3 Principle ... 5
4 Reagents and Materials ... 5
5 Apparatus ... 7
6 Analytical Procedures ... 7
7 Calculation of Results ... 8
8 Tolerance ... 8
9 Test Report ... 8
Appendix A (Informative) Methods of Waste Liquid Treatment ... 10
Foreword
GB/T 11213 Sodium Hydroxide for Chemical Fiber Use can be divided into the following parts:
--- Part 1: Sodium Hydroxide for Chemical Fiber Use – Determination of Sodium Hydroxide
Content;
--- Part 2: Sodium Hydroxide for Chemical Fiber Use – Determination of Sodium Chloride
Content – Spectrometric Method;
--- Part 3: Sodium Hydroxide for Chemical Fiber Use – Determination of the Calcium Mass
Fraction – EDTA Complexometric Method;
--- Part 4: Sodium Hydroxide for Chemical Fiber Use – Determination of Silicon Content –
Reduced Molybdosilicate Spectrophotometric Method;
--- Part 5: Sodium Hydroxide for Chemical Fiber Use – Determination of Sulphate Content;
--- Part 7: Sodium Hydroxide for Chemical Fiber Use – Determination of Copper Content –
Spectrometric Method.
This Part is Part 2 of GB/T 11213, which corresponds to the Japanese Standard JIS K 1200-3-
1:2000 Sodium Hydroxide for Industrial Use – Part 3: Determination of Chlorides Content –
Section 1: Mercury (II) Thiocyanate Photometry (Japanese Version). The consistency between
this Part and JIS K 1200-3-1:2000 is modified to use.
The major differences between this Part and Japanese Standard JIS K 1200-3-1:2000 are as
follows:
--- The applicable sodium chloride content range is different;
--- Add absolute ethanol to increase dissolution and stability when preparing mercury
thiocyanate solution, and improve color rendering effect;
--- Adjust the preparation operation method according to the range of sodium chloride
content in the specimen;
--- The representation method of sodium chloride standard solution is different;
--- The result calculation formula is changed;
--- The content of waste liquid treatment is given in the form of appendix.
This Part replaced GB/T 11213.2-1989 Sodium Hydroxide for Chemical Fiber Use –
Determiantion of Sodium Chloride Content – Spectrometric Method.
Compared with GB/T 11213.2-1989, the major changes of this Part are as follows:
Sodium Hydroxide for Chemical Fiber Use – Determination
of Sodium Chloride Content – Spectrometric Method
1 Scope
This Part of GB/T 11213 specifies the method for the determination of sodium chloride content
in sodium hydroxide for chemical fiber use.
This Part applies to products with a sodium chloride content of 0.0002% ~ 0.02% in sodium
hydroxide.
2 Normative References
The provisions in following documents become the provisions of this Part through reference in
this Part. For dated references, the subsequent amendments (excluding corrigendum) or
revisions do not apply to this Part, however, parties who reach an agreement based on this Part
are encouraged to study if the latest versions of these documents are applicable. For undated
references, the latest edition of the referenced document applies.
GB/T 603 Chemical Reagent – Preparations of Reagent Solution for Use in Test Methods
(GB/T 603-2002, ISO 6353-1:1982, NEQ)
GB/T 6682 Water for Laboratory Use – Specifications (GB/T 6682-1992, neq ISO
3696:1987)
3 Principle
Chloride ions (Cl-) in the specimen completely replace thiocyanate (SCN-) in mercury
thiocyanate; and the substituted thiocyanate (SCN-) reacts with ferric nitrate to form ferric
thiocyanate, which appears red; at the wavelength of 450 nm, the colored solution is
photometrically measured. The reaction formula is as follows:
4 Reagents and Materials
The reagents and water used in this method are all analytical reagents and third-grade water
specified in GB/T 6682 or water of corresponding purity. The standard solutions, preparations
and products required in the test shall be prepared according to the provisions of GB/T 603,
except those specified in this Part. The preparation, storage, sampling and determination of
reagents shall be carried out in an environment free of chlorine and hydrogen chloride.
4.1 Nitric acid.
4.2 Iron nitrate [Fe(NO3)3 • 9H2O].
4.3 Hydrogen peroxide.
4.4 Ferric nitrate solution: 8g/L (calculated as Fe).
Choose one of the two preparation methods of ferric nitrate solution.
Method 1: In a 500mL conical flask, add about 4.0g of pure iron (purity >99.5%), accurate to
0.01g. Add 80mL of water; then carefully add 80mL of nitric acid (4.1); and slowly heat the
solution in the hood until it boils. After the reaction is complete and all the nitrous acid gas has
been driven off; add a few drops of hydrogen peroxide (4.3) to decolorize the solution. Continue
to boil for 2 min; stop heating; after cooling off, transfer all the solution into a 500mL
volumetric flask; dilute with water to the mark, and shake well.
Method 2: In a 500mL conical flask, add about 29.0g of ferric nitrate [Fe(NO3)3 • 9H2O],
accurate to 0.01g. Add 60mL of water; then carefully add 60mL of nitric acid (4.1); slowly heat
the solution in the hood until it boils. After the reaction is complete and all the nitrous acid gas
has been driven off; add a few drops of hydrogen peroxide (4.3) to decolorize the solution.
Continue to boil for 2 min; stop heating; after cooling off, transfer all the solution into a 500mL
volumetric flask; dilute with water to the mark, and shake well.
4.5 Mercury thiocyanate solution: 0.5g/L.
Weigh 0.1g of mercury thiocyanate [Hg(SCN)2], accurate to 0.001g. Put it in a 250mL beaker;
add 30mL of absolute ethanol; and add 150mL of warm water under constant stirring to dissolve
it. Then filter the solution into a 200mL volumetric flask; dilute to the mark with water; and
shake well.
4.6 Sodium chloride standard solution: 0.1mg/mL.
Weigh 0.1g of sodium chloride standard reagent that has been pre-burned at 500°C ~ 600°C to
constant weight, accurate to 0.0001g. Put it in a beaker; add a small amount of water to dissolve
it; and then transfer the entire solution into a 1000mL volumetric flask. Dilute to the mark with
water and shake well.
4.7 Sodium chloride standard solution: 0.01mg/mL.
Pipette 20.0mL of sodium chloride standard solution (4.6); place it in a 200mL volumetric flask;
dilute with water to the mark; and shake well.
4.8 Phenolphthalein indicator solution: 10g/L.
5 Apparatus
General laboratory instruments and spectrophotometers.
6 Analytical Procedures
6.1 Drawing of standard curve
6.1.1 Preparation of standard colorimetric solution
Pipette 0.0mL, 2.0mL, 4.0mL, 6.0mL, 8.0mL, 10.0mL, 12.0mL, 15.0mL of sodium chloride
standard solution (4.7) in sequence; respectively placed in 50mL volumetric flasks; then, in
each volumetric flask, add 5mL of nitric acid (4.1), 5mL of ferric nitrate solution (4.4) and
20mL of mercuric thiocyanate solution (4.5); dilute to the mark with water; shake well; let stand
for 30min to develop color.
6.1.2 Determination of absorbance of standard colorimetric solution
Use a spectrophotometer at a wavelength of 450nm; adjust the zero point of the
spectrophotometer with water; and use a 4cm or 5cm absorption cell to measure the absorbance.
6.1.3 Drawing of standard curve
Take the mass (mg) of sodium chloride in the 50mL of standard colorimetric solution as the
abscissa, and the corresponding absorbance as the ordinate, subtract the absorbance of the blank
solution; and draw the standard curve.
6.2 Preparation of specimen solution
6.2.1 Weigh a solid or liquid laboratory sample equivalent to 20g of sodium hydroxide, accurate
to 0.01g; dissolve it in a 200mL volumetric flask with water; and dilute to the mark; and shake
well.
6.2.2 When the mass of sodium chloride in the 50mL of standard colorimetric solution is greater
than 0.15mg, pipette the specimen solution in 6.2.1; dilute it by an appropriate multiple; and
perform the measurement according to 6.4. The calculation result is based on the dilution factor
of the specimen solution, and Formula (1) is multiplied by the corresponding dilution factor.
6.3 Blank test
The blank test is carried out at the same time as the specimen measurement; and the
measurement procedure and the used amount of reagent are the same as those for the specimen
......
Source: Above contents are excerpted from the PDF -- translated/reviewed by: www.chinesestandard.net / Wayne Zheng et al.
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