Iso 3210 2010
Iso 3210 2010
Iso 3210 2010
STANDARD 3210
Third edition
2010-07-01
Reference number
ISO 3210:2010(E)
© ISO 2010
ISO 3210:2010(E)
PDF disclaimer
This PDF file may contain embedded typefaces. In accordance with Adobe's licensing policy, this file may be printed or viewed but
shall not be edited unless the typefaces which are embedded are licensed to and installed on the computer performing the editing. In
downloading this file, parties accept therein the responsibility of not infringing Adobe's licensing policy. The ISO Central Secretariat
accepts no liability in this area.
Adobe is a trademark of Adobe Systems Incorporated.
Details of the software products used to create this PDF file can be found in the General Info relative to the file; the PDF-creation
parameters were optimized for printing. Every care has been taken to ensure that the file is suitable for use by ISO member bodies. In
the unlikely event that a problem relating to it is found, please inform the Central Secretariat at the address given below.
Contents Page
Foreword ............................................................................................................................................................iv
1 Scope ......................................................................................................................................................1
2 Principle..................................................................................................................................................1
3 Reagents.................................................................................................................................................1
4 Apparatus ...............................................................................................................................................2
5 Preparation of test piece.......................................................................................................................2
6 Procedure ...............................................................................................................................................2
6.1 Method 1 .................................................................................................................................................2
6.2 Method 2 .................................................................................................................................................3
7 Expression of results ............................................................................................................................4
8 Test report ..............................................................................................................................................4
Annex A (normative) Method for the drying of samples.................................................................................5
Bibliography........................................................................................................................................................6
iTeh STANDARD PREVIEW
(standards.iteh.ai)
ISO 3210:2010
https://standards.iteh.ai/catalog/standards/sist/adef2cb5-6be4-4841-b077-
5b754718efde/iso-3210-2010
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies
(ISO member bodies). The work of preparing International Standards is normally carried out through ISO
technical committees. Each member body interested in a subject for which a technical committee has been
established has the right to be represented on that committee. International organizations, governmental and
non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the
International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2.
The main task of technical committees is to prepare International Standards. Draft International Standards
adopted by the technical committees are circulated to the member bodies for voting. Publication as an
International Standard requires approval by at least 75 % of the member bodies casting a vote.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. ISO shall not be held responsible for identifying any or all such patent rights.
ISO 3210 was prepared by Technical Committee ISO/TC 79, Light metals and their alloys, Subcommittee
SC 2, Organic and anodic oxidation coatings on aluminium.
iTeh STANDARD PREVIEW
This third edition cancels and replaces the second edition (ISO 3210:1983), which has been technically
revised. (standards.iteh.ai)
ISO 3210:2010
https://standards.iteh.ai/catalog/standards/sist/adef2cb5-6be4-4841-b077-
5b754718efde/iso-3210-2010
1 Scope
This International Standard specifies methods of assessing the quality of sealed anodic oxidation coatings on
aluminium and its alloys by measurement of the loss of mass after immersion in phosphoric acid/chromic acid
solution.
⎯ Method 1: assessment of quality of sealed anodic oxidation coatings by measurement of the loss of mass
after immersion in phosphoric acid/chromic acid solution, without prior acid treatment.
⎯
iTeh STANDARD PREVIEW
Method 2: assessment of quality of sealed anodic oxidation coatings by measurement of the loss of mass
(standards.iteh.ai)
after immersion in phosphoric acid/chromic acid solution with prior acid treatment.
Method 1 is applicable to anodic oxidation coatings intended for decorative or protective purposes or where
resistance to staining is important.
ISO 3210:2010
https://standards.iteh.ai/catalog/standards/sist/adef2cb5-6be4-4841-b077-
Method 2 is applicable to anodic oxidation 5b754718efde/iso-3210-2010
coatings intended for architectural purposes. For less severe
applications, Method 1 may be more suitable.
⎯ anodic oxidation coatings that have been sealed only in dichromate solutions;
⎯ anodic oxidation coatings that have undergone a treatment to render them hydrophobic.
NOTE The methods are destructive and can serve as reference methods in case of doubt or dispute regarding the
results of the test for loss of absorptive power (see ISO 2143[1]), or the measurement of admittance (ISO 2931[2]).
2 Principle
An unsealed anodic oxidation coating on aluminium is dissolved rapidly by acid media, whereas a well-sealed
coating will withstand long immersion without appreciable attack.
3 Reagents
Use only reagents of recognized analytical grade and distilled water or deionized water.
NOTE This solution can be obtained, for example, by diluting a 65 % nitric acid solution (ρ20 = 1,40 g/ml) with an
equal volume of water.
Aqueous solution containing per litre, 35 ml of phosphoric acid (ρ20 = 1,7 g/ml) and 20 g of chromium(VI)
oxide.
WARNING — Chromium(VI) is toxic and shall be handled properly. Chromium(VI) solutions are
hazardous to the environment and severely hazardous to waters.
4 Apparatus
Usual laboratory apparatus and glassware, together with the following.
6 Procedure
6.1 Method 1
6.1.1 Measure the total coated area of the test piece (excluding cut edges and other uncoated surfaces).
NOTE The test solution does not attack bare metal and it is not necessary to take uncoated surfaces into account.
Remove any surface bloom from the test piece by rubbing with a dry cloth.
6.1.2 Degrease the test piece in an organic solvent, e.g. acetone or ethanol (96 %), at room temperature
according to the method specified in A.1.
6.1.3 Dry the test piece thoroughly in accordance with A.1 and A.2 and weigh immediately to the nearest
0,1 mg (mass m1).
6.1.4 Immerse the test piece completely, standing upright, in the test solution (see 3.2) and leave it for
exactly 15 min at a constant temperature of 38 °C ± 1 °C.
Uniformity of temperature within the test solution is very important; this can be achieved by using a water-bath
and stirring continuously.
Do not use the test solution after more than 4,5 g of anodic oxidation coating have been dissolved per litre of
solution.
Do not use the test solution which has been in contact with materials other than anodized aluminium or its
alloys.
6.1.5 Take the test piece from the test solution and rinse thoroughly, first under running water and then in
distilled water or deionized water. Dry the test piece as specified in Annex A and weigh immediately to the
nearest 0,1 mg (mass m2).
6.1.6 During the operations described in 6.1.2 to 6.1.5, avoid touching the test piece with bare hands.
Take extreme care that the two drying operations required in 6.1.3 and 6.1.5 are carried out in the same
reproducible way and avoid heating to temperatures above 60 °C.
6.2 Method 2
6.2.1 Measure the total coated area of the test piece (excluding cut edges and other uncoated surfaces).
NOTE The predip and test solution do not attack bare metal and it is not necessary to take uncoated surfaces into
account.
6.2.2 Degrease the test piece in an organic solvent, e.g. acetone or ethanol (96 %), at room temperature
according to the method specified in A.1.
6.2.6 Immerse the test piece completely, standing it upright, in the test solution (see 3.2) and leave for
exactly 15 min at a constant temperature of 38 °C ± 1 °C.
NOTE Uniformity of temperature within the test solution is very important; this can be achieved by using a water-bath
and stirring continuously.
Do not use the test solution after more than 4,5 g of anodic oxidation coating have been dissolved per litre of
solution.
Do not use the test solution which has been in contact with materials other than anodized aluminium or its
alloys.
6.2.7 Take the test piece from the test solution and rinse it thoroughly, first under running water and then in
distilled water or deionized water. Dry the test piece as specified in Annex A and weigh immediately to the
nearest 0,1 mg (mass m2).
6.2.8 During the operations described in 6.2.2 to 6.2.7, avoid touching the test piece with bare hands.
Take extreme care that the two drying operations required in 6.2.3 and 6.2.7 are carried out in the same
reproducible way and avoid heating to temperatures above 60 °C.
7 Expression of results
Calculate the loss in mass of surface δA, in milligrams per square decimetre, using Equation (1):
m1 − m 2
δA = (1)
A
where
m1 is the mass, in milligrams, of the test piece before immersion in the (predip and) test solution;
m2 is the mass, in milligrams, of the test piece after immersion in the (predip and) test solution;
A is the coated surface area of the test piece, in square decimetres, in contact with the (predip and)
test solution.
8 Test report
The test report shall include at least the following information:
NOTE Acceptance levels will normally be specified in the relevant product specification.
Annex A
(normative)
A.1 Degrease the test piece by gentle agitation for 30 s in a organic solvent, e.g. acetone or ethanol (96 %),
at room temperature, remove, leave for 5 min in the ambient atmosphere (pre-drying), place in a drying oven
preheated to 60 °C and leave for exactly 15 min with the coated surfaces standing upright.
WARNING — Where organic solvents are used, carry out the degreasing operation and the pre-drying
in a well-ventilated area to minimize exposure to solvent vapour.
A.2 Allow the test piece to cool for 30 min over silica gel in a closed desiccator.
A.3 After the acid treatment and rinsing (see 6.1.5 and 6.2.7), repeat operations A.1 and A.2, omitting the
use of organic solvent.