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D171058 Jen PDF
D171058 Jen PDF
D17 1058 / - - J
This document is to be considered as a whole, the parts of which shall not be separated.
"Seul le texte franais fait foi, les traductions ntant faites que pour en faciliter lemploi".
"The French text alone is valid. The translations are provided to assist the reader in understanding the standards".
RENAULT 2009.
No duplication permitted without the consent of the issuing department.
No circulation permitted without the consent of RENAULT.
CREATION
MODIFICATIONS
QUOTED DOCUMENTS
CONTENT
Page
2. PRINCIPLE 5
3.2. AIR 5
3.4. COLLECTORS 6
3.10. SUPPORTS 8
4. SALT SOLUTION 9
4.3. PREPARATION 9
7. PREPARATION OF SAMPLES 11
7.1. SAMPLING: 11
7.3. PROTECTION: 11
I7.4. MATURATION 11
7.5. STOVING : 12
9. OPERATING CONDITIONS 13
CONTENT (continued)
Page (continued)
10. QUOTATION OF SAMPLES DURING THE TEST 13
17. TRAINING 16
ANNEX 1: METHOD OF CHECK AND MONITORING THE AGGRESSIVITY 17
1. PERIODICITY 17
2. OPERATING CONDITIONS 17
2.4. SAVINGS 18
FOREWORD
This test method incorporates the results of work conducted in France by a working group comprising salt spray
test users of various sectors (CBBS):
- Automobile manufacturers,
- cabinet manufacturers,
- CETIM.
This method is applicable to laboratory specimens, parts or samplings of vehicle parts, elements that
we shall group together in this test method under the term "samples".
2. PRINCIPLE
The salt spray test consists in a corrosive attack accelerated by an artificial salt spray of defined
composition and pluviometry (quantity of salt solution sprayed), under precise conditions of
temperature and pressure.
Any change of appearance must be written in the final test report (cosmetic deterioration)
The water used for the preparation of the salt solution and for the filling of the saturator shall be
deionized with conductivity lower than 20 S / cm measured at 23C 2C.
3.2. AIR
The compressed air shall be oil-free and filtered to avoid the presence of particles. This air is qualified
as follows:
Metal or organic particles and stains lower than 0,2 mg / m and of diameter lower than 5 m.
Minimum purity of the sodium chloride: 99,8 % (w). The sodium chloride shall not contain, in the
anhydrous state, more than 0,2 % of impurities and more than 0,1 % of sodium iodide. It shall be free
of copper and nickel (less than 10mg / kg for each of these elements).
3.4. COLLECTORS
Use as collection devices smoother funnels of diameter 10 cm placed on graduated test tubes of a
sufficient volume to collect the quantity of condensates between two measures.
The constituent materials of the collection set shall be made from chemically inert material towards the
salt solution (glass, polymer).
The collectors are used for the daily checks of the pluviometry, the measures of the monthly and
annual aggressivity.
Daily check: 1 at least, in that case, please change the place of the collector after every
measure to verify the conformity of the pluviometry on all the testing area.
Measure of the monthly aggressivity: 1 collector placed near the reference plate.
Measure of the annual aggressivity: 3 collectors placed near every reference plates.
The materials of the equipment that are in contact with the salt solution shall be made from chemically
inert material towards the salt solution.
Volume in which the specifications in term of temperature, pluviometry and aggressivity are in
accordance with the requirements described in this test method. Thus, it is the volume in
which samples can be explained during the salt spray test.
Height
Front view
Top view
Depth
3
The chamber of spraying shall have a minimal capacity of 0,4 m . The fog must be distributed in a
uniform way, whatever is the load of the cabinet. The upper part of the chamber must be designed so
that the accumulated drops of solution, which stream on the surface, shall not run on the tested
samples. Walls and cover can be isolated if it is necessary for a good regulation of the temperature
and thus for the homogeneity of the size of the droplets of fog in all the volume of the cabinets.
The quantity of solution collected in every collector must be between 1 ml / hour and 2 ml / hour, for a
horizontal area of recovery of 78,5 cm (for a funnel 10 cm in diameter).
The solution sprayed during the test is evacuated at the lower point of the tank.
An appropriate device has to maintain the temperature in the range of 35 C 2 C in the useful
volume of the test chamber and its content. This is to avoid the phenomena of condensation of the fog
on the walls of the cabinet.
The spraying system consists of a supply of clean compressed air, under appropriate pressure and
humidity; one or several atomizers and an optional opaque tank made from chemically inert material
towards the salt solution.
The pressure of spraying must be in the range of 0,8 bar to 1,6 bar, according to the
recommendations of the manufacturer. A high pressure promotes a homogeneous distribution of the
fog in the test chamber.
The water inside the saturator has to be in accordance with the definition given in the present Test
method at the paragraph 3.1.
After going through the saturator, the compressed air must be saturated in water to prevent the rise of
chloride mass concentration in the fog: the air is moistened before being sprayed by passing through
the saturator containing water warmed to a temperature superior to that of the chamber (45 C -
47C). The equipment has to guarantee the saturatio n of the air with water. The filling and the
stabilization at a constant level of water in the bubble tower have to be made with some deionized
water. The saturator must be equipped with a thermometer to measure the temperature of the water
and an outlet that could permit to check the conductivity of the water.
IMPORTANT: Check the high level of water inside the bubble tower to be sure that water is not
sprayed with the salt solution (risk of dilution of chloride concentration in the fog) ; and collect in a
beaker the solution sprayed after the atomizer and to check the pH and the NaCl concentration of the
collected solution.
The temperature of the saturator must be in the range from 45C to 47C.
The air quality can be indirectly controlled by measuring the conductivity of the water in the saturator.
If the conductivity evolves beyond 20 S / cm, the saturator will be drained away, cleaned and it will be
necessary to check the air supply.
Recommendation: The temperature and the conductivity of the water in the saturator can be daily
recorded in a monitoring document dedicated to the cabinet.
Atomizers must be made from chemically inert material towards the salt solution. Their configuration
will be adapted to the cabinet; so that it can assure the uniformity of the distribution of the fog in the
whole useful volume of the chamber.
For the cabinet equipped with an internal tank of salt solution, the level of the solution in this tank
(placed inside or outside of the chamber of spraying) should remain constant to assure a regular
supply of fog during all the duration of the test.
3.10. SUPPORTS
Supports for samples must be made from chemically inert material towards the salt solution (for
example PVC).
Any water dropping on samples supports (resulting for example from water retention on the tubes
supplying salt solution and air) is not acceptable.
The tanks of preparation, of use and the agitators must be entirely made from chemically inert material
towards the salt solution. Tanks will be opaque to avoid the formation of algae and equipped with
filters.
4. SALT SOLUTION
The solution that is used to the spraying during this test is a solution of 5 % 0,5 % (50g / l 5g /
l) of NaCl of density between 1,025 and 1,040 and in a pH range from 6,0 to 7,5.
After prepared, the salt solution must not be stirred during the test.
4.3. PREPARATION
Do not prepare the salt solution in the tank of use during a test running, in order to eliminate any
risk of pollution of samples tested in case of error of preparation.
To avoid this risk a solution consists in using two tanks. The first one is dedicated to the
preparation of the salt solution: TANK OF PREPARATION and the other one is the TANK OF
USE ". The prepared salt solution can be transferred only when the solution is in compliance with
the requirements (cf. diagram below).
TANK OF
PREPARATION TANK OF USE
Filters
- Pour the quantity of deionized water wanted (conductivity less than 20 S / cm).
- Add the calculated quantity of salt (50g / l 5g / l).
- Stir the solution.
- When the salt is dissolved, check the concentration of the solution and adjust it if needed.
- Wait at least 4 hours by stirring.
- Measure the pH of the solution.
- If the pH is not correct: leave the solution another 4 hours under stirring and then re-measure
it. If after 2 x 4 hours of stabilization under stirring the pH does not fit the requirement,
the solution may not be used and shall be discarded. In that case, the purity of the salt
and the conductivity of the water must be verified.
The solution must be clear and limpid (visual observation); if necessary filter it. The solution prepared
is ready to be used after transfer it in the tank of use.
To validate the solution, the density or the concentration in salt is measured and recorded after every
preparation.
To control the reliability and the reproducibility of the results obtained in a cabinet or to compare the
results coming from various cabinets, it is necessary to check the aggressivity of the test chambers.
The method to assess the aggressivity of the test chamber is joined in Annex 1; it defines in particular
the parameters of reference plates:
- Number and position of agressivity plates and collector sets in the cabinet,
The VERIFICATION must be realized in an empty cabinet, at least once a year, and after
maintenance works or important repairs of the equipment.
The MONTHLY MONITORING must be realized according to the load inside the cabinet. In case of
impossibility to control, indicate it in the book of monitoring of the cabinet.
Parameters Requirements
pH 6,0 to 7,5
Aggressivity Note 2 or 3
7. PREPARATION OF SAMPLES
7.1.SAMPLING:
The number, the type, the shape and the dimension of samples must be chosen according to the
rules of specification of the material or the product tested. If there is no specification, validation
criteria have to be found between the involved people before the test.
Samples must not be cleaned before launch in test except opposite specification: case of samples
deliberately covered with greasy protector films (oil, greases) or samples presenting an important
pollution (oil, lubricant). In those cases, the method to use depends on the nature of the material,
on the surface and on the products that contaminated this surface. Abrasives and solvents which
could attack the surface of the sample shall not be used. Check visually all the samples before
the test.
7.3.PROTECTION:
If samples to be tested are cut from bigger coated parts, the cut has to be made carefully in order
not to damage the coating close to the cut. Except opposite specification, the edges of the cut must
be protected by an appropriate and inert protection, such as wax, paint or adhesive tape.
7.4.MATURATION
The salt spray test must be performed only after a minimum period of 24 hours following the
coating of the part.
7.5.STOVING :
If the samples to be tested have to undergo a stoving before corrosion test (case of certain motor
specifications), the conditions will be the following ones:
- The salt spray test can be made as soon as specimens and parts are back to room temperature.
Samples shall be placed in the useful volume of the chamber but not in the direct flux of the sprayed
fog.
The angle under which the surface is exposed in the chamber is very important. The sample must be
placed in the chamber of spraying with the tested side upward, by forming with the vertical line an
angle of 20 5. In the case of sample of irregular shape, we h ave to take into account, as possible,
this recommendation and limit the quotation to the correctly directed surface
Samples to be tested shall not be in contact with the walls of the cabinet. The surfaces to be tested
must be exposed to the free circulation of the fog. Samples can be placed at various levels of the
useful volume of the chamber, on the condition of no superimposing. The orientation of samples must
not be modified in the course of test. However, in every daily control, it is possible to switch samples.
Samples
Bar of
fixation
Runnings
Running
Sample to be tested (ex: screw)
Samples on
support
Suspended samples
The materials of the supports serving for exposing the samples must be made from chemically inert
material towards the salt solution. Samples must be fixed during all the duration of the test. In the
particular case of fasteners, it is recommended to fix parts by assembly on adapted plates support. In
that case the implanted zone of the screw in the support will be not taken into account during the
quotations.
9. OPERATING CONDITIONS
The test can only be performed in a cabinet in compliance with the requirements of the present test
method. The temperatures (chamber and saturator), pressure of air and pluviometry have to comply
with the specifications during all the duration of the test.
The recordings of the test conditions will be written in the DAILY MONITORING REPORT (Cf. Annex
8).
Date
Setting value of the cabinet during the check (Pressure of the air, Flow rate of the salt
solution)
Volume of condensates
Observations
Samples can be daily controlled but necessarily without rinsing. They will be dried either at ambient air
outdoors or with clean and cold air or with an inert gas (N2, Ar) or with an absorbent paper.
The duration of the quotation of samples has not to exceed one hour a day. This duration is not
deducted from the exposure time of samples.
At the end of the test, remove the samples from the chamber; eliminate carefully the residues of
sprayed solution deposited on the surface. We can, for that purpose, proceed by rinsing or by
immersion of the samples in tap water, at a temperature not exceeding 37 C. Dry them at once using
a cold and clean source of air or an inert gas (N2, Ar) or with an absorbent paper.
The test performance can be appraised through different criteria, according to the particular
requirements written in the specifications of the material or of the tested product:
- Presence of white oxidation (products of corrosion: zinc, zinc alloys, coatings on zinc base,
aluminum, magnesium ),
- Runnings,
- Visual quotation of the corroded surface or the density of pitting / unity of surface,
The test report has to record the information on the following points:
- The date of the last annual and\or monthly measurement of the aggressivity and the date of the
next one,
- The duration of the test and the results of the possible intermediary controls,
- The average result obtained on all the samples of the tested batch,
The test report has to mention all the deviations with regard to the present test method as well as
all the incidents during the test.
14.1. PERIODICITY
These verifications must be made every 12 weeks if the occupation rate of the means allows it
and at least twice a year. They are performed with an empty cabinet.
14.2. VERIFICATION
Verification of the temperature of regulation inside the chamber and if possible of the
temperature inside the saturator after a minimum of 4 hours of stabilization (cf. Annex 7).
Verification of the pluviometry in the net volume of the cabinet (cf. annex 6).
The volume of condensate inside at least one collector placed the day before inside the
cabinet.
The temperature of regulation of the chamber. In the absence of indicator on the cabinet,
place a temperature sensor (Pt100) in the chamber and make a measurement after one hour
minimum of stabilization. In that case the measurement of the temperature has to be made at
a minimal distance of 100 mm from walls and as high as the tested samples. The sensor can
be placed in a PVC tube to avoid its deterioration. A continuous monitoring by a sensor
independent from the regulation system is recommended.
The value of the density or the concentration of salt in the salt solution.
IMPORTANT: The control of the pH and the concentration of NaCl must be necessarily
performed in the solution taken in the tank of use. It can be sensible to control the pH of the
solution sprayed to be sure that water from saturator is not sprayed with the salt solution, that
could cause a dilution of the salt concentration.
Write these values on the daily monitoring report of the cabinet (see example in annex 8) and
compare with the cabinet verification settings.
In case of drift of one or some of the initial parameters make the adjustments and\or the necessary
modifications.
If possible, transfer the samples in another cabinet certified for the salt spray test. If the
duration of the breakdown is more than 48 hours, realize a quotation of the samples then rinse
them in deionized water, dry them and place them in desiccators.
Under this condition, samples can be kept 7 days. After this deadline the samples shall be
discarded.
Before the restart of the test, it is advised to make a new quotation of the samples to be sure
that there was no evolution of the oxidation.
In every case, every incident and\or breakdowns as well as an evolution of the oxidation must be
indicated in the final test report.
17. TRAINING
The users of cabinets must have received an internal training including in particular an information
about the various standards, the functioning principle of a cabinet, the preparation of the salt solution,
the measurement of pH, the maintenance and the verification of the cabinet, the verification and the
monitoring of the aggressivity of the cabinet, the method of evaluation of the result, the writing of the
test reports. The training report will be formalized and archived.
ANNEX 1
INTRODUCTION
This protocol has for objective to verify the aggressivity of a salt spray chamber. It fixes the
parameters identified as critics in the studies led within the framework of the CBBS. It fixes the
conditions in which the cabinet or its settings are considered in agreement with the test method and
establishes an aggressivity level. This one will be expressed in the form of a note and written on the
test report.
1. PERIODICITY
The ANNUAL VERIFICATION OF THE AGGRESSIVITY aims at controlling the cabinet on the totality
of the useful volume and independently of any test on any part. It is thus performed with an empty
cabinet.
The MONITORING OF THE AGGRESSIVITY is performed every month if the occupation rate of the
cabinet allows it, and at least 4 times a year, for measuring the performances of the cabinet. It can be
performed in a cabinet with a test running.
- to the results of the tests performed within the framework of the CBBS,
NOTE: Reference plates used in this method are not linked with a chain of calibration.
2. OPERATING CONDITIONS
Reference plates are steel DC 04 according to the NF EN 10338 standard, coated with a zinc layer
obtained by hot galvanization on continuous line.
The zinc thickness is 10 m 1 m. Plates can be covered with a film of oil, in order to insure a better
preservation.
ANNEX 1 (NEXT)
. Temperature 45 C ( 2 C)
The lifetime of this solution is 36 months in opaque packaging and in storage conditions from 0C to
40C. The solution of degreasing must be stocked in a closed package when it is not used. One liter of
solution can degrease up to 5 plates.
3. After ultrasound degreasing, take out the plate by means of tongs, rinse it under water then in the
ethanol and let it dry in the air.
2.4. SAVINGS
The degreased plates will be manipulated with gloves. The borders of plates as well as the back can
be protected with a typical adhesive tape: Havane 100 mm x 38 mm, according to annex 2.
The support must be realized in chemically inert material. It will allow to position plates according to
the appropriate angle (20 5 with regard to th e vertical line). The center of the plate will be situated
at the height at the atomizer. The number and the position of plates vary according to the test and the
design of the cabinet (Cf. Annex 5 and 5 suite):
- At least 3 plates during the ANNUAL VERIFICATION. They will be positioned in a quarter, one half
and three quarters of the distance between the atomizer and the most distant wall, the side to be
corroded facing the atomizer,
- At least 1 plate during the MONTHLY MONITORING, the plate will be positioned halfway between
the atomizer and the most distant wall of the cabinet.
ANNEX 1 (NEXT)
Orientation of plates:
Plates
Support
The collectors are positioned near the reference plates. (Cf. Annex 4 and 4 next)
The recommendations above in term of number of plates and positioning are to be adapted
according to the useful area of the cabinet.
During the ANNUAL VERIFICATION, the cabinet has to contain only reference plates.
During the MONTHLY MONITORING, the test is performed in the conditions of filling required by the
in-going test. The other exposed samples shall not hide the reference plates (no recovering).
Reproduce on a transparency the mask of measure given in Annex 2. Put the mask on the reference
plate and count the number of oxidized squares. Consider a square as oxidized as soon as it presents
at least one point of red oxidation, included a running from another square (Cf. Annex 3).
The first control will be made visually, necessarily between 70 and 72 hours and then every 24
hours on not rinsed, wet plate.
In the case of the annual verification, the opening of the cabinet shall not last more than 30 min every
day.
In the case of the monthly monitoring, every quotation of the samples has not to exceed 1 hour a day.
This time is not deducted from the exposure time.
ANNEX 1 (NEXT)
We indicate by TRO (Time of Red Oxidation) the time before the first observation of a red level of
oxidation upper to 5 %, which are 6 squares at least.
The typical report given in Annex 4 must be filled in its totality by indicating necessarily: the note of the
aggressivity, the percentage of oxidation and the exposure time of plates for every quotation.
ANNEX 2
20
5 5
10
ANNEX 3
Top of Plate
=
Top of Mask 4 3
7 8
10 9 Mask of
control
11
15 14 13 12
18
16 17
20 19
26 25
27 22 21
30 29 28 24 23
33 31
32
35 34
ANNEX 4
AGRESSIVITY REPORT OF THE TEST CHAMBER
pH =
Concentration of NaCl:
The measures are to be made on the salt solution in the tank of use and not in the collectors.
(*): Volume of the condensates in every collector divided by the total duration of the test (included time of
opening)
(**): The reference number of the collector corresponds to the number of the tested reference plate.
Remarks
ANNEX 5
Atomizer
Atomizer
3/4 L
L L
Note: L = Distance between the atomizer and the most distant wall.
ANNEX 5 (suite)
Plate 3 Collector 3
1/2 L
Plate 2
Atomizer Atomizer
3/4 L 1/2 L
1/4 L
Collector 1
Collector 2 Collector
Plate 1
L L
Note: L = Distance between the atomizer and the most distant wall.
ANNEX 6
C1 100 C3
C2
=
100 100
=
C6 C4
C5
100
C1 to C6 : collectors
Dimension in mm
ANNEX 7
Front view
Side view
Sensor n1
Height
Sensor n2
Sensor n3
Top view
Sensors 1, 2 et 3 Depth
Lenght
The number of temperature sensors shall be adapted to the useful volume of the
cabinet
ANNEX 8