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GB/T 19719-2005Jewellery -- Determination of the release of nickel -- Method of spectrometry (English PDF)

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Issued by

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

Level / Type

National · Recommended

Issue date

March 23, 2005

Implementation date

September 1, 2005

Scope

GB/T 19719-2005 (Jewellery -- Determination of the release of nickel -- Method of spectrometry) is available as an English-translated PDF.

GB/T 19719-2005 - This Standard specifies a method for simulating the release of nickel from jewellery, in order to determine whether the item releases nickel at a rate greater than 0.5 µg/(cm2·week).

This Standard is applicable to the determination of the release of nickel from jewellery, as well as the products intended to come into direct and prolonged contact with the skin (see

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Document preview — GB/T 19719-2005

National Standard of the People's Republic of China

ICS
39.060
Classification
Y 88

Issued by: General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

Contents

  • Foreword...3
  • 1 Scope...4
  • 2 Normative References...4
  • 3 Principle...4
  • 4 Reagents...4
  • 5 Apparatus...5
  • 6 Samples...6
  • 7 Procedure...7
  • 8 Calculations...8
  • 9 Test Report...9
  • Appendix A...10
  • Appendix B...12
  • Appendix C...14
  • Appendix D...15
  • Appendix E...16
  • Appendix F...17

Foreword

This Standard is modified in relation to European Standard EN 1811.1998 "Reference Test

Method for Release of Nickel from Products Intended to Come into Direct and Prolonged

Contact with the Skin" (English edition).

In order to be convenient for application, this Standard makes the following editorial changes.

a) "This European Standard" was changed into "this Standard";

b) The comma "," served as decimal point is replaced by the decimal point ".";

c) "cm3" is replaced by "mL";

d) The Foreword of the international standard was deleted;

e) Add Appendix E (Informative) for guidance.

Appendixes A, B, C, D, E and F of this Standard are informative.

This Standard was proposed by China National Light Industry Council.

This standard shall be under the jurisdiction of National Technical Committee on Jewellery of

Standardization Administration of China (SAC/TC 256).

Drafting organizations of this Standard. National Jewellery Quality Supervision and

Inspection Center, National Center of Quality Supervision & Inspection on Gold-Silver

Products (Nanjing), and National Center of Quality Supervision & Inspection on Gold-Silver

Products (Shanghai).

Chief drafting staffs of this Standard. Li Wujun, Wang Donghui, Fang Mingxu, Fan Jifang, Li

Yukun, and Li Suqing.

Jewellery - Determination of the Release of

Nickel - Method of Spectrometry

1 Scope

This Standard specifies a method for simulating the release of nickel from jewellery, in order

to determine whether the item releases nickel at a rate greater than 0.5 µg/(cm2·week).

This Standard is applicable to the determination of the release of nickel from jewellery, as

well as the products intended to come into direct and prolonged contact with the skin (see

4.3.2 of GB 11887-2002).

2 Normative References

The following normative documents contain provisions which, through reference in this text,

constitute provisions of this Standard. For dated references, subsequent amendments to, or

revisions of, any of these publications do not apply. However, parties to agreements based on

this Standard are encouraged to investigate the possibility of applying the most recent editions

of the normative documents indicated below. For undated references, the latest edition of the

normative document referred to applies.

GB 11887-2002 Jewellery - Fineness of Precious Metal Alloys and Designation (ISO

9202.1991, NEQ)

3 Principle

The item to be tested for nickel release is placed in an artificial sweat test solution for one

week. The concentration of dissolved nickel in the solution is determined by atomic

absorption spectrometry, inductively-coupled plasma spectrometry or other appropriate

analytical method. The nickel release is expressed in micrograms per square centimetre per

week [µg/(cm2·week)].

4 Reagents

Except where indicated, all reagents, distilled water or deionized water or equivalent shall be

of recognized analytical pure grade.

4.1 Sodium chloride.

4.2 Urea.

4.6 Nitric acid. 65 % (m/m), rho = 1.40 g/mL..

4.7 Dilute ammonia solution. 1%(m/m). Transfer 10 mL of ammonia solution (4.5) into a

250 mL beaker containing 100 mL of deionized water. Stir and cool to room temperature.

Transfer the solution to a 250 mL volumetric flask and make up to the volume with deionized

water.

4.8 Dilute nitric acid. approximately 5 % (m/m). Transfer 15 mL of nitric acid (4.6) into a

500 mL beaker containing 100 mL of deionized water (4.3). Stir and cool to room temperature.

Transfer the solution to a 250 mL volumetric flask and make up to the volume with deionized

water.

5 Apparatus

5.1 A pH-meter, accurate to ±0.02 pH.

5.2 An analytical spectrometer. The instrument shall, after optimization, meet the

performance criteria given in 5.2.1 and 5.2.2.It is recommended that either an

inductively-coupled plasma-optical emission spectrometer or an electrothermal excitation

atomic absorption spectrometer is used.

5.2.1 Minimum precision. The standard deviation of 10 measurements of the absorption of a

full matrix calibration solution containing 0.05 mg nickel per litre shall not exceed 10 %.

5.3 Thermostatically controlled water-bath or oven, capable of maintaining a temperature of

(30 ± 2) °C.

5.4 A vessel with lid, both composed of a non-metallic, nickel-free and nitric-acid-resistant

material, such as glass and/or polypropylene and/or polytetrafluoroethylene and/or

polystyrene.

6 Samples

6.1 Sample area

6.1.1 Definition of sample area

Only the surfaces of an item that comes into direct and prolonged contact with the skin shall

be analyzed. In this standard such surfaces are defined as "sample area".

6.2 Sample preparation

Gently swirl the sample for 2 min in degreasing solution (4.9) at room temperature. Rinse

thoroughly with deionized water and dry. After degreasing, items should be handled with

plastic forceps or clean protective gloves.

6.3 Reference disc

As a quality control check, the nickel release from a reference disc may be determined (see

Appendix B).

7 Procedure

7.1 Preparation of test solution

7.1.1 Preparation of deionized and aerated water

Fill a tall-form 2 L beaker with deionized water (4.3), saturate with air by attaching a gas

distribution tube to a cork and positioning the lower end of the tube on the bottom of the

beaker.

7.1.2 Preparation of artificial sweat

The artificial sweat consists of deionized and aerated water containing.

7.2 Release procedure

7.2.1 Place the sample, suspended by its holder, in the test vessel (5.4). Add an amount of

test solution corresponding to approximately 1 mL per cm2 sample area. The suspended

sample shall be totally immersed. However, it is not essential to immerse areas which are

completely protected by wax or lacquer.

7.3 Determination of nickel

Determine the nickel content of the test solution using an analytical spectrometer (see 5.2).

7.4 Number of replicates

Whenever possible, the determination shall be carried out on at least two identical samples.

8 Calculations

8.1 Nickel release

The nickel release of a sample, d, expressed in micrograms per square centimetre per week

[µg/(cm2·week)], is given by the equation.

8.2 Interpretation of results

Multiply the result, d, established in 8.1 by 0.1 to obtain an adjusted analytical figure. A

sample shall be deemed to have a nickel release of more than 0.5 µg/(cm2·week) if the

adjusted figure is greater than 0.5 µg/(cm2·week).

9 Test Report

- identification of the sample including source, date of receipt, form;

- reference standard (include issued or published year);

- for each replicate, the nickel release and its adjusted figure, which can be calculated

according to the requirement of Chapter 8;

- if relevant, details of any deviations from this standard method;

- any unusual features observed during the determination;

- date of test;

- identification of laboratory carrying out the analysis;

- signature of laboratory manager and operator.

Appendix A

(Informative)

Statistical Uncertainty of the Test Procedure and Interpretation of Results

Most chemical test methods are designed to measure the total amount of a substance in a

material. This usually makes it possible to obtain an accurate result with close statistical

agreement between laboratories because there is an absolute or true value. The test method in

this Standard measures the rate of soluble nickel release from an item. With this type of

chemical test the result is dependent upon the specified conditions of test, and there is no

absolute or true value. Consequently, it is more difficult to obtain close statistical agreement

between laboratories when performing such migration (or release) tests.

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This preview omits tables, figures, formulas and parts of the technical clauses. The complete document — 17 pages — is available in the English PDF.

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