1007/2011 - Regulation (EU) No 1007/2011 of the European Parliament and of the Council of 27 September 2011 on textile fibre names and related labelling and marking of the fibre composition of textile products and repealing Council Directive 73/44/EEC and Directives 96/73/EC and 2008/121/EC of the European Parliament and of the Council

This document specifies methods of quantitative analysis of various ternary mixtures of fibres.
The field of application of each method for analysing mixtures, specified in the parts of ISO 1833, indicates the fibres to which the method is applicable.
This document is applicable to mixtures of fibres with more than three components provided that the combination of test methods leads back to simple cases of fibre mixtures. Table B.1 illustrates the typical ternary mixtures and their applied corresponding parts of the ISO 1833 series.

This document specifies a common method for the quantitative chemical analysis of various mixtures of fibres. This method and the methods described in the other parts of ISO 1833 are applicable, in general, to fibres in any textile form. Where certain textile forms are excepted, these are listed in the scope of the appropriate part.

This document specifies a method, using sulfuric acid, to determine the mass percentage of polyamide, after removal of non-fibrous matter, in textiles made of binary mixtures of
—     polyamide
with
—polypropylene/polyamide bicomponent.

This document specifies a method, using concentrated sulfuric acid, to determine the mass percentage of chlorofibres and certain other fibres, after removal of non-fibrous material, in textiles made of mixtures of
—     cotton, viscose, cupro, modal, lyocell, acetate, triacetate, polyamide, polyester, elastomultiester, certain acrylic and certain modacrylic fibres
with
—     chlorofibres (based on homopolymers of vinyl chloride), polypropylene, elastolefin, melamine and polypropylene/polyamide bicomponent.
The modacrylics concerned are those which give a clear solution when immersed in concentrated sulfuric acid.
This method can be used, particularly in place of the methods described in ISO 1833-12 and ISO 1833-13, in all cases where a preliminary test shows that the chlorofibres do not dissolve completely either in dimethylformamide or in the azeotropic mixture of carbon disulfide and acetone.

This document specifies a common method for the quantitative chemical analysis of various mixtures
of fibres. This method and the methods described in the other parts of ISO 1833 are applicable, in
general, to fibres in any textile form. Where certain textile forms are excepted, these are listed in the
scope of the appropriate part.

This document specifies methods of quantitative analysis of various ternary mixtures of fibres.
The field of application of each method for analysing mixtures, specified in the parts of ISO 1833,
indicates the fibres to which the method is applicable.
This document is applicable to mixtures of fibres with more than three components provided that
the combination of test methods leads back to simple cases of fibre mixtures. Table B.1 illustrates the
typical ternary mixtures and their applied corresponding parts of the ISO 1833 series.

This document describes a pneumatic pressure method for the determination of bursting strength and bursting distension of textile fabrics.
NOTE    ISO 13938-1 describes a method using hydraulic pressure.
The method is applicable to knitted, woven, nonwoven and laminated fabrics. It can be suitable for fabrics produced by other techniques. The test is suitable for test specimens in the conditioned or wet state.
From the available data there appears to be no significant difference in the bursting strength results achieved using hydraulic or pneumatic burst testers, for pressures up to 800 kPa. This pressure range covers the majority of performance levels expected of general apparel. For speciality textiles requiring high bursting pressures, the hydraulic apparatus is more suitable.

This document describes a hydraulic method for the determination of bursting strength and bursting distension of textile fabrics.
In this document, a hydraulic pressure is applied using a constant rate of pumping device.
NOTE    ISO 13938-2 describes a method using pneumatic pressure.
The method is applicable to knitted, woven, nonwoven and laminated fabrics. It can be suitable for fabrics produced by other techniques. The test is suitable for test specimens in the conditioned or wet state.
From the available data, there appears to be no significant difference in the bursting strength results achieved using hydraulic or pneumatic burst testers, for pressures up to 800 kPa. This pressure range covers the majority of performance levels expected of general apparel. For speciality textiles requiring high bursting pressures, the hydraulic apparatus is more suitable.

This document specifies a method, by determining the nitrogen content, to calculate the proportion of each component, after the removal of non-fibrous matter, in textiles made of mixtures of
—     jute
with
—     animal fibres.
The animal-fibre component can consist solely of hair or wool, or of any mixtures of the two.
This document is not applicable to products in which dyestuffs or finishes contain nitrogen.
NOTE    Because this method differs in principle from the general method based on selective solubility set out in ISO 1833-1, it is given in a form that is complete in itself.

This document specifies a method, using carbon disulfide/acetone, to determine the mass percentage of chlorofibre, after removal of non-fibrous matter, in textiles made of mixtures of
—          certain chlorofibres,
with
—     wool, animal hair, silk, cotton, viscose, cupro, modal, lyocell, polyamide, polyester, elastomultiester, acrylic, melamine, polypropylene, polypropylene/polyamide bicomponent, polyacrylate and glass fibres.
It is also possible to analyse mixtures containing chlorofibres by using the test methods described in ISO 1833-17 or ISO 1833-21.

This document specifies a method, using glacial acetic acid, to determine the mass percentage of acetate, after removal of non-fibrous matter, in textiles made of mixtures of
—     acetate
with
—     certain chlorofibres or after-chlorinated chlorofibres.
It is also possible to analyse mixtures containing acetate by using the test methods described in ISO 1833-3 or ISO 1833-9.

This document specifies a method, using benzyl alcohol, to determine the mass percentage of acetate, after removal of non-fibrous matter, in textiles made of mixtures of
—     acetate
with
—          triacetate, polypropylene, elastolefin, melamine, polypropylene/polyamide bicomponent and polyacrylate fibres.

EN-ISO 1833-17 specifies a method, using concentrated sulfuric acid, to determinethe mass percentage of chlorofibres and certain other fibres, after removal ofnon-fibrous material, in textiles made of mixtures of - cotton, viscose, cupro,modal, lyocell, acetate, triacetate, polyamide, polyester, elastomultiester,certain acrylic and certain modacrylic fibres with - chlorofibres (based onhomopolymers of vinyl chloride), polypropylene, elastolefin, melamine andpolypropylene/polyamide bicomponent. The modacrylics concerned are those whichgive a clear solution when immersed in concentrated sulfuric acid. This methodcan be used, particularly in place of the methods described in ISO 1833-12 andISO 1833-13, in all cases where a preliminary test shows that the chlorofibresdo not dissolve completely either in dimethylformamide or in the azeotropicmixture of carbon disulfide and acetone.

This document specifies a method, using xylene, to determine the mass percentage of polypropylene, after removal of non-fibrous matter, in textiles made of mixtures of
—          polypropylene fibres
with
—          wool, animal hair, silk, cotton, viscose, cupro, modal, lyocell, acetate, triacetate, polyamide, polyester, acrylic, glass fibres, elastomultiester, melamine and polyacrylate.

This Standard describes a pneumatic pressure method for the determination of bursting strength and bursting distension of textile fabrics. The method is applicable to knitted, woven, nonwoven and laminated fabrics. It can be suitable for fabrics produced by other techniques. The test is suitable for test specimens in the conditioned or wet state. From the available data there appears to be no significant difference in the bursting strength results achieved using hydraulic or pneumatic burst testers, for pressures up to 800 kPa. This pressure range covers the majority of performance levels expected of general apparel.

This Standard describes a hydraulic method for the determination of bursting strength and bursting distension of textile fabrics. In this document, a hydraulic pressure is applied using a constant rate of pumping device. The method is applicable to knitted, woven, nonwoven and laminated fabrics. It can be suitable for fabrics produced by other techniques. The test is suitable for test specimens in the conditioned or wet state. From the available data, there appears to be no significant difference in the bursting strength results achieved using hydraulic or pneumatic burst testers, for pressures up to 800 kPa. This pressure range covers the majority of performance levels expected of general apparel. For speciality textiles requiring high bursting pressures, the hydraulic apparatus is more suitable.

This standard specifies a method, by determining the nitrogen content, to calculate the proportion of each component, after the removal of non-fibrous matter, in textiles made of mixtures of - jute with - animal fibres. The animal-fibre component can consist solely of hair or wool, or of any mixtures of the two. This document is not applicable to products in which dyestuffs or finishes contain nitrogen.

This document specifies a method, using dichloromethane, to determine the mass percentage of triacetate or polylactide, after removal of non-fibrous matter, in textiles made of mixtures of
—          triacetate or polylactide
with
—          wool or other animal hair, silk, protein, cotton, viscose, cupro, modal,lyocell, polyamide, polyester, acrylic, elastomultiester, polypropylene, elastolefin, melamine, polypropylene/polyamide bicomponent,polyacrylate and glass fibres.
Triacetate fibres which have been partially hydrolysed (i.e. saponification) cease to be completely soluble in the reagent. In such cases, this method is not applicable.

This document specifies a method, using cyclohexanone, to determine the mass percentage of chlorofibre, modacrylic, elastane, acetate and triacetate, after removal of non-fibrous matter, in textiles made of mixtures of
—          acetate, triacetate, chlorofibre, certain modacrylics, certain elastanes
with
—                                      wool, animal hair, silk, cotton, cupro, modal, viscose, lyocell, polyamide, acrylic, melamine, polyacrylate and glass fibres.
It is also possible to analyse mixtures containing chlorofibres by using the test methods described in ISO 1833-13 or ISO 1833-17.

This document specifies a method, using glacial acetic acid, to determine the mass percentage of acetate, after removal of non-fibrous matter, in textiles made of mixtures of - acetate with - certain chlorofibres or after-chlorinated chlorofibres. It is also possible to analyse mixtures containing acetate by using the test methods described in ISO 1833-3 or ISO 1833-9.

This document specifies a method, using carbon disulfide/acetone, to determine the mass percentage of chlorofibre, after removal of non-fibrous matter, in textiles made of mixtures of - certain chlorofibres, with - wool, animal hair, silk, cotton, viscose, cupro, modal, lyocell, polyamide, polyester, elastomultiester, acrylic, melamine, polypropylene, polypropylene/polyamide bicomponent, polyacrylate and glass fibres. It is also possible to analyse mixtures containing chlorofibres by using the test methods described in ISO 1833-17 or ISO 1833-21.

This document specifies a method, using benzyl alcohol, to determine the mass percentage of acetate, after removal of non-fibrous matter, in textiles made of mixtures of - acetate with - triacetate, polypropylene, elastolefin, melamine, polypropylene/polyamide bicomponent and polyacrylate fibres.

This document specifies a method, using a mixture of formic acid and zinc chloride, to determine the mass percentage of viscose, certain types of cupro, modal or lyocell, after removal of nonfibrous matter, in textiles made of mixtures of
—          viscose, certain types of cupro, modal or lyocell,
with
—          cotton.
This document has been initially specifically established for mixtures of viscose, certain types of cupro, modal or lyocell with cotton, it is also applicable to mixtures with polypropylene, elastolefin and melamine.
IMPORTANT — If a cupro or modal or lyocell fibre is found to be present, a preliminary test is carried out to see whether it is soluble in the reagent.
The method is not applicable to mixtures in which the cotton has suffered extensive chemical degradation. It is not applicable when the viscose, cupro, modal or lyocell fibre is rendered incompletely soluble by the presence of certain permanent finishes or reactive dyes that cannot be removed completely.

This document specifies a method using dimethylacetamide to determine the mass percentage of elastane, after removal of non-fibrous matter, in textiles made of mixtures of:
—          certain elastane fibres
with
—          cotton, viscose, cupro, modal, lyocell, polyamide, polyester or wool fibres.
This method is not applicable when acrylic fibres are present.
It is also possible to analyse mixtures containing certain elastane fibres by using the test methods described in ISO 1833-12 or ISO 1833-21.

This document specifies a method, using dichloromethane, to determine the mass percentage of
triacetate or polylactide, after removal of non-fibrous matter, in textiles made of mixtures of
— triacetate or polylactide
with
— wool or other animal hair, silk, protein, cotton, viscose, cupro, modal,lyocell, polyamide, polyester,
acrylic, elastomultiester, polypropylene, elastolefin, melamine, polypropylene/polyamide
bicomponent,polyacrylate and glass fibres.
Triacetate fibres which have been partially hydrolysed (i.e. saponification) cease to be completely
soluble in the reagent. In such cases, this method is not applicable.

This document specifies a method, using cyclohexanone, to determine the mass percentage of
chlorofibre, modacrylic, elastane, acetate and triacetate, after removal of non-fibrous matter, in textiles
made of mixtures of
— acetate, triacetate, chlorofibre, certain modacrylics, certain elastanes
with
— wool, animal hair, silk, cotton, cupro, modal, viscose, lyocell, polyamide, acrylic, melamine,
polyacrylate and glass fibres.
It is also possible to analyse mixtures containing chlorofibres by using the test methods described in
ISO 1833-13 or ISO 1833-17.

ISO 1833-11:2017 specifies a method, using sulfuric acid, to determine the mass percentage of cellulose fibres, after removal of non-fibrous matter, in textiles made of mixtures of
-      natural and man-made cellulose fibres, such as cotton, flax, hemp, ramie, viscose, cupro, modal, lyocell
with
-      polyester, polypropylene, elastomultiester, elastolefin and polypropylene/polyamide bicomponent.

ISO 1833-7:2017 specifies a method, using formic acid, to determine the mass percentage of polyamide fibre, after removal of non-fibrous matter, in textiles made of mixtures of
-      polyamide
with
-      cotton, viscose, cupro, modal, lyocell, polyester, polypropylene, chlorofibre, acrylic, glass fibre, elastomultiester, elastolefin and melamine, or
-      wool (if the wool content is less than or equal to 25 %), or animal hair fibres.
ISO 1833-7:2017 does not apply when the wool content exceeds 25 %; ISO 1833-4 applies.

ISO 1833-4:2017 specifies a method, using hypochlorite, to determine the mass percentage of protein fibre, after removal of non-fibrous matter, in textiles made of mixtures of certain non-protein fibres and certain protein fibres, as follows:
-      wool, other animal-hair (such as cashmere, mohair), silk, protein,
with
-      cotton, cupro, viscose, modal, acrylic, chlorofibres, polyamide, polyester, polypropylene, glass, elastane, elastomultiester, elastolefin, melamine and polypropylene/polyamide bicomponent.

This document specifies a method, using acetone, to determine the mass percentage of acetate, after removal of non-fibrous matter, in textiles made of mixtures of
— acetate with
— wool, animal hair, silk, regenerated protein, cotton (scoured, kiered, or bleached), flax (or linen), hemp, jute, abaca, alfa, coir, broom, ramie, cupro, viscose, modal, polyamide, polyester, acrylic, elastolefin, elastomultiester, melamine, polypropylene/polyamide bicomponent, polyacrylate and glass fibres.
It is not applicable to mixtures containing modacrylic fibres, nor to mixtures containing acetate fibres that have been deacetylated on the surface.

This document specifies a method, using acetone, to determine the mass percentage of acetate, after removal of non-fibrous matter, in textiles made of mixtures of
— acetate
with
— wool, animal hair, silk, regenerated protein, cotton (scoured, kiered, or bleached), flax (or linen), hemp, jute, abaca, alfa, coir, broom, ramie, cupro, viscose, modal, polyamide, polyester, acrylic, elastolefin, elastomultiester, melamine, polypropylene/polyamide bicomponent, polyacrylate and glass fibres.
It is not applicable to mixtures containing modacrylic fibres, nor to mixtures containing acetate fibres that have been deacetylated on the surface.

This document specifies a method, using dimethylformamide, to determine the mass percentage of acrylic, modacrylic, chlorofibre or elastane, after removal of non-fibrous matter, in textiles made of mixtures of
— acrylic, certain modacrylics, certain chlorofibres, certain elastane fibres
with
— wool, animal hair, silk, cotton, viscose, cupro, modal, lyocell, polyamide, polyester, elastomultiester, elastolefin, melamine, polyacrylate or glass fibres.
It is not applicable to animal hair, wool and silk dyed with chromium based mordant dyes.
NOTE Dyestuff identification is described in ISO 16373-1[3].

This document specifies a method, using sulfuric acid, to determine the mass percentage of silk, after removal of non-fibrous matter, in textiles made of binary mixtures of
— silk
with
— other protein fibres (e.g. wool or animal hair).