32007L0004•Commission Directive 2007/4/EC of 2 February 2007 amending, for the purposes of its adaptation to technical progress, Annex II to Directive 96/73/EC of the European Parliament and of the Council on certain methods for quantitative analysis of binary textile fibre mixtures (Text with EEA relevance )
32007L0004DirectiveFeb 23, 2007
of 2 February 2007
amending, for the purposes of its adaptation to technical progress, Annex II to Directive 96/73/EC of the European Parliament and of the Council on certain methods for quantitative analysis of binary textile fibre mixtures
(Text with EEA relevance)
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Directive 96/73/EC of the European Parliament and of the Council of 16 December 1996 on certain methods for quantitative analysis of binary textile fibre mixtures 1 , and in particular Article 5(2) thereof,
Whereas:
(1) Directive 96/74/EC of the European Parliament and the Council of 16 December 1996 on textile names 2 requires labelling to indicate the fibre composition of textile products, with checks being carried out by analysis on the conformity of these products with indications given on the label.
(2) Uniform methods for quantitative analysis of binary textile fibre mixtures are provided for in Directive 96/73/EC.
(3) On the basis of recent findings by the technical working group, Directive 96/74/EC was adapted to technical progress, by adding the fibre elastolefin to the list of fibres set out in Annexes I and II to that Directive.
(4) It is therefore, necessary to define uniform test methods for elastolefin.
(5) Directive 96/73/EC should therefore be amended accordingly.
(6) The measures provided for in this Directive are in accordance with the opinion of the Committee for Directives relating to Textile Names and Labelling,
HAS ADOPTED THIS DIRECTIVE:
Annex II to Directive 96/73/EC is amended in accordance with the Annex to this Directive.
1. Member States shall bring into force the laws, regulations and administrative provisions necessary to comply with this Directive by 2 February 2008 at the latest. They shall forthwith communicate to the Commission the text of those provisions and a correlation table between those provisions and this Directive. When Member States adopt those provisions, they shall contain a reference to this Directive or be accompanied by such a reference on the occasion of their official publication. Member States shall determine how such reference is to be made.
2. Member States shall communicate to the Commission the text of the main provisions of national law which they adopt in the field covered by this Directive.
This Directive shall enter into force on the 20th day following its publication in the Official Journal of the European Union .
This Directive is addressed to the Members States.
Done at Brussels, 2 February 2007. For the Commission Günter VERHEUGEN Vice-President
1 OJ L 32, 3.2.1997, p. 1 . Directive as last amended by Commission Directive 2006/2/EC ( OJ L 5, 10.1.2006, p. 10 ).
2 OJ L 32, 3.2.1997, p. 38 . Directive as last amended by Commission Directive 2006/3/EC ( OJ L 5, 10.1.2006, p. 14 ).
Annex II to Directive 96/73/EC is amended as follows:
| 1. | (a): In point I.3 ‘materials and equipment’ the following entries are inserted: ‘I.3.2.4 Acetone I.3.2.5 Orthophosphoric acid I.3.2.6 Urea I.3.2.7 Sodium bicarbonate’. — ‘I.3.2.4 — Acetone — I.3.2.5 — Orthophosphoric acid — I.3.2.6 — Urea — I.3.2.7 — Sodium bicarbonate’. ‘I.3.2.4: Acetone I.3.2.5: Orthophosphoric acid I.3.2.6: Urea I.3.2.7: Sodium bicarbonate’. | (a) | ‘I.3.2.4: Acetone | ‘I.3.2.4 | Acetone | I.3.2.5 | Orthophosphoric acid | I.3.2.6 | Urea | I.3.2.7 | Sodium bicarbonate’. | (b) | Point I.6 ‘Pre-treatment of laboratory test sample’ is replaced by the following: ‘Where a substance not to be taken into account in the percentage calculations (see Article 12(3) of Directive 96/74/EC of the European Parliament and of the Council of 16 December 1996 on textile names) is present, it should first be removed by a suitable method that does not affect any of the fibre constituents. For this purpose, non-fibrous matter which can be extracted with light petroleum and water is removed by treating the air-dry test sample in a Soxhlet extractor with light petroleum for one hour at a minimum rate of six cycles per hour. Allow the light petroleum to evaporate from the sample, which is then extracted by direct treatment consisting in soaking the specimen in water at room temperature for one hour and then soaking it in water at 65 ± 5 °C for a further hour, agitating the liquor from time to time. Use a liquor:specimen ratio of 100:1. Remove the excess water from the sample by squeezing, suction or centrifuging and then allow the sample to become air-dry. In the case of elastolefin or fibre mixtures containing elastolefin and other fibres (wool, animal hair, silk, cotton, flax, true hemp, jute, abaca, alfa, coir, broom, ramie, sisal, cupro, modal, protein, viscose, acrylic, polyamide or nylon, polyester, elastomultiester) the procedure just described should be slightly modified, in fact light petroleum ether should be replaced by acetone. In the case of binary mixtures containing elastolefin and acetate the following procedure shall apply as pre-treatment. Extract the specimen for 10 minutes at 80 °C with a solution containing 25 g/l of 50 % orthophosphoric acid and 50 g/l of urea. Use a liquor:specimen ratio of 100:1. Wash the specimen in water, then drain and wash it in a 0,1 % sodium bicarbonate solution, finally wash it carefully in water. Where non-fibrous matter cannot be extracted with light petroleum and water, it should be removed by substituting for the water method described above a suitable method that does not substantially alter any of the fibre constituents. However, for some unbleached, natural vegetable fibres (e.g. jute, coir) it is to be noted that normal pre-treatment with light petroleum and water does not remove all the natural non-fibrous substances; nevertheless additional pre-treatment is not applied unless the sample does contain finishes insoluble in both light petroleum and water. Analysis reports shall include full details of the methods of pre-treatment used.’ |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| (a) | ‘I.3.2.4: Acetone | ‘I.3.2.4 | Acetone | I.3.2.5 | Orthophosphoric acid | I.3.2.6 | Urea | I.3.2.7 | Sodium bicarbonate’. | ||||
| ‘I.3.2.4 | Acetone | ||||||||||||
| I.3.2.5 | Orthophosphoric acid | ||||||||||||
| I.3.2.6 | Urea | ||||||||||||
| I.3.2.7 | Sodium bicarbonate’. | ||||||||||||
| (b) | Point I.6 ‘Pre-treatment of laboratory test sample’ is replaced by the following: ‘Where a substance not to be taken into account in the percentage calculations (see Article 12(3) of Directive 96/74/EC of the European Parliament and of the Council of 16 December 1996 on textile names) is present, it should first be removed by a suitable method that does not affect any of the fibre constituents. For this purpose, non-fibrous matter which can be extracted with light petroleum and water is removed by treating the air-dry test sample in a Soxhlet extractor with light petroleum for one hour at a minimum rate of six cycles per hour. Allow the light petroleum to evaporate from the sample, which is then extracted by direct treatment consisting in soaking the specimen in water at room temperature for one hour and then soaking it in water at 65 ± 5 °C for a further hour, agitating the liquor from time to time. Use a liquor:specimen ratio of 100:1. Remove the excess water from the sample by squeezing, suction or centrifuging and then allow the sample to become air-dry. In the case of elastolefin or fibre mixtures containing elastolefin and other fibres (wool, animal hair, silk, cotton, flax, true hemp, jute, abaca, alfa, coir, broom, ramie, sisal, cupro, modal, protein, viscose, acrylic, polyamide or nylon, polyester, elastomultiester) the procedure just described should be slightly modified, in fact light petroleum ether should be replaced by acetone. In the case of binary mixtures containing elastolefin and acetate the following procedure shall apply as pre-treatment. Extract the specimen for 10 minutes at 80 °C with a solution containing 25 g/l of 50 % orthophosphoric acid and 50 g/l of urea. Use a liquor:specimen ratio of 100:1. Wash the specimen in water, then drain and wash it in a 0,1 % sodium bicarbonate solution, finally wash it carefully in water. Where non-fibrous matter cannot be extracted with light petroleum and water, it should be removed by substituting for the water method described above a suitable method that does not substantially alter any of the fibre constituents. However, for some unbleached, natural vegetable fibres (e.g. jute, coir) it is to be noted that normal pre-treatment with light petroleum and water does not remove all the natural non-fibrous substances; nevertheless additional pre-treatment is not applied unless the sample does contain finishes insoluble in both light petroleum and water. Analysis reports shall include full details of the methods of pre-treatment used.’ |
| 2. | (a): The Special Methods – Summary Table is replaced by the following: ‘2. SPECIAL METHODS — SUMMARY TABLE Methods Field of application Reagent Soluble component Insoluble component No 1 Acetate Certain other fibres Acetone No 2 Certain protein fibres Certain other fibres Hypochlorite No 3 Viscose, cupro or certain types of modal Cotton or elastolefin Formic acid and zinc chloride No 4 Polyamide or nylon Certain other fibres Formic acid, 80 % m/m No 5 Acetate Triacetate or elastolefin Benzyl alcohol No 6 Triacetate or polylactide Certain other fibres Dichloromethane No 7 Certain cellulose fibres Polyester, elastomultiester or elastolefin Sulphuric acid, 75 % m/m No 8 Acrylics, certain modacrylics or certain chlorofibres Certain other fibres Dimethylformamide No 9 Certain chlorofibres Certain other fibres Carbon disulphide/acetone, 55,5/44,5 v/v No 10 Acetate Certain chlorofibres or elastolefin Glacial acetic acid No 11 Silk Wool, hair or elastolefin Sulphuric acid, 75 % m/m No 12 Jute Certain animal fibres Nitrogen content method No 13 Polypropylene Certain other fibres Xylene No 14 Certain other fibres Chlorofibres (homopolymers of vinyl chloride) or elastolefin Concentrated sulphuric acid method No 15 Chlorofibres, certain modacrylics, certain elastanes, acetates, triacetates Certain other fibres Cyclohexanone’ — Methods — Field of application — Reagent — Soluble component — Insoluble component — No 1 — Acetate — Certain other fibres — Acetone — No 2 — Certain protein fibres — Certain other fibres — Hypochlorite — No 3 — Viscose, cupro or certain types of modal — Cotton or elastolefin — Formic acid and zinc chloride — No 4 — Polyamide or nylon — Certain other fibres — Formic acid, 80 % m/m — No 5 — Acetate — Triacetate or elastolefin — Benzyl alcohol — No 6 — Triacetate or polylactide — Certain other fibres — Dichloromethane — No 7 — Certain cellulose fibres — Polyester, elastomultiester or elastolefin — Sulphuric acid, 75 % m/m — No 8 — Acrylics, certain modacrylics or certain chlorofibres — Certain other fibres — Dimethylformamide — No 9 — Certain chlorofibres — Certain other fibres — Carbon disulphide/acetone, 55,5/44,5 v/v — No 10 — Acetate — Certain chlorofibres or elastolefin — Glacial acetic acid — No 11 — Silk — Wool, hair or elastolefin — Sulphuric acid, 75 % m/m — No 12 — Jute — Certain animal fibres — Nitrogen content method — No 13 — Polypropylene — Certain other fibres — Xylene — No 14 — Certain other fibres — Chlorofibres (homopolymers of vinyl chloride) or elastolefin — Concentrated sulphuric acid method — No 15 — Chlorofibres, certain modacrylics, certain elastanes, acetates, triacetates — Certain other fibres — Cyclohexanone’ Methods: Field of application — Reagent Soluble component: Insoluble component No 1: Acetate — Certain other fibres — Acetone No 2: Certain protein fibres — Certain other fibres — Hypochlorite No 3: Viscose, cupro or certain types of modal — Cotton or elastolefin — Formic acid and zinc chloride No 4: Polyamide or nylon — Certain other fibres — Formic acid, 80 % m/m No 5: Acetate — Triacetate or elastolefin — Benzyl alcohol No 6: Triacetate or polylactide — Certain other fibres — Dichloromethane No 7: Certain cellulose fibres — Polyester, elastomultiester or elastolefin — Sulphuric acid, 75 % m/m No 8: Acrylics, certain modacrylics or certain chlorofibres — Certain other fibres — Dimethylformamide No 9: Certain chlorofibres — Certain other fibres — Carbon disulphide/acetone, 55,5/44,5 v/v No 10: Acetate — Certain chlorofibres or elastolefin — Glacial acetic acid No 11: Silk — Wool, hair or elastolefin — Sulphuric acid, 75 % m/m No 12: Jute — Certain animal fibres — Nitrogen content method No 13: Polypropylene — Certain other fibres — Xylene No 14: Certain other fibres — Chlorofibres (homopolymers of vinyl chloride) or elastolefin — Concentrated sulphuric acid method No 15: Chlorofibres, certain modacrylics, certain elastanes, acetates, triacetates — Certain other fibres — Cyclohexanone’ |
|---|
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"title": "Commission Directive 2007/4/EC of 2 February 2007 amending, for the purposes of its adaptation to technical progress, Annex II to Directive 96/73/EC of the European Parliament and of the Council on certain methods for quantitative analysis of binary textile fibre mixtures (Text with EEA relevance )",
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