🧂 Salt spray corrosion test

Automotive PN-EN ISO 9227

Accelerated corrosion test in salt spray chamber. Three methods: NSS (neutral), AASS (acetic acid), and CASS (with copper chloride). Assessment of corrosion resistance of metals and protective coatings.

Overview

The salt spray test is one of the oldest and most widely used accelerated methods for assessing the corrosion resistance of metallic materials and protective coatings. ISO 9227 defines three test variants: NSS (Neutral Salt Spray), AASS (Acetic Acid Salt Spray), and CASS (Copper-Accelerated Acetic Acid Salt Spray).

In the automotive industry, the salt spray test is a standard qualification test for galvanic coatings (zinc, nickel, chromium), paint coatings, anodic oxide layers, and conversion protective coatings. OEMs (BMW, VW, Toyota, Stellantis) require suppliers to provide confirmed corrosion resistance of chassis, body, connector, and fastener elements.

The NSS method (5% NaCl, pH 6.5–7.2, 35°C) is most common and used for most metals and coatings. AASS (pH 3.1–3.3 with acetic acid) is more aggressive and intended for testing decorative Cu/Ni/Cr coatings. CASS (with CuCl₂ addition) is the fastest method — exposure usually does not exceed 48 hours, making it an economical alternative to long-term NSS tests.

Important: ISO 9227 defines only the apparatus, reagents, and procedure — it does not specify acceptance criteria, exposure time, or result evaluation method. These parameters are defined in product standards and OEM specifications (e.g., VW TL 211, BMW GS 90011).

Method principle

In a closed climate chamber, a controlled fog (aerosol) is generated from a sodium chloride (NaCl) solution. The solution is sprayed through pneumatic nozzles fed by compressed air, creating a uniform fog that settles on samples placed at an angle of 15–25° from vertical. Chamber temperature is maintained at 35±2°C (NSS and AASS) or 50±2°C (CASS). Condensing brine creates a thin electrolytic film on sample surfaces, which initiates and sustains electrochemical corrosion processes (formation of galvanic micro-cells). After a specified exposure time, samples are removed, rinsed, dried, and visually or instrumentally assessed for degree of corrosion, blistering, flaking, or coating adhesion loss.

Applications

Key parameters

ParameterValue
NaCl concentration (NSS/AASS)50 ± 5 g/L (5%)
NSS solution pH6.5–7.2 (at 25°C)
AASS solution pH3.1–3.3 (glacial acetic acid)
NSS/AASS chamber temperature35 ± 2°C
CASS chamber temperature50 ± 2°C
Fog settling rate1.0–2.0 mL/h per 80 cm² (horizontal collector)

Standard

Standard number
PN-EN ISO 9227:2017
Title (PL)
Badania korozyjne w sztucznych atmosferach — Badania w rozpylonej solance
Title (EN)
Corrosion tests in artificial atmospheres — Salt spray tests

Step-by-step procedure

1. Salt solution preparation

Dissolve 50±5 g NaCl in 950 mL deionized water. For AASS — add acetic acid to pH 3.1–3.3. For CASS — additionally 0.26 g/L CuCl₂·2H₂O.

⏱ Time: 30 min • 🌡 Temperature: 25°C

2. Solution pH check

Measure solution pH at temperature 25±2°C. NSS: 6.5–7.2, AASS: 3.1–3.3, CASS: 3.1–3.3. Correct with NaOH or HCl if necessary.

⏱ Time: 10 min • 🌡 Temperature: 25°C

3. Sample preparation

Clean samples of dirt and grease (do not remove coating!). Protect cut edges and areas not subject to testing with protective tape or wax.

⏱ Time: 15–30 min

4. Placing samples in chamber

Set samples at angle 15–25° from vertical. Do not allow mutual dripping. Place fog collectors.

⏱ Time: 10 min

5. Test start

Set chamber temperature (35°C NSS/AASS, 50°C CASS). Start spraying. Check fog settling rate (1–2 mL/h/80 cm²) after first 24 h.

⏱ Time: 15 min • 🌡 Temperature: 35°C or 50°C

6. Monitoring during test

Daily check solution level, temperature, and fog settling rate. Replenish solution. Do not open chamber without necessity.

⏱ Time: continuous

7. End of exposure

After required time (24 h, 48 h, 96 h, 240 h, 480 h, 720 h, 1000 h — according to specification) remove samples from chamber.

⏱ Time: per specification

8. Sample rinsing and drying

Gently rinse samples with running water (temperature <40°C) to remove salt deposits. Dry at room temperature.

⏱ Time: 15 min • 🌡 Temperature: <40°C

9. Result assessment

Assess degree of corrosion according to reference standards (ISO 10289, ISO 4628, ASTM D1654). Document: blistering, flaking, white/red rust, percentage of corroded surface.

⏱ Time: 30–60 min

10. Photographic documentation and report

Take photos of samples before and after test. Prepare report with test parameters, exposure time, visual assessment, and compliance result with requirements.

⏱ Time: 30 min

Required equipment and apparatus

EquipmentExampleIndicative price
Salt spray chamberAscott S450, Weiss Technik SC/KWT, Erichsen 606/608, Atlas CCX40 000–200 000 PLN
Air compressor with filtrationAtlas Copco, FIAC, pressure 0.7–1.4 bar, oil-free5 000–15 000 PLN
Laboratory pH meterMettler Toledo SevenCompact, WTW inoLab pH 73103 000–10 000 PLN
Analytical balanceMettler Toledo ME204, Sartorius Quintix 2245 000–15 000 PLN
Fog collectorsGlass funnels Ø80 mm with graduated cylinder, 2 pcs according to standard200–500 PLN/pc
Sample racks / holdersGlass or plastic (PP, PTFE), angle 15–25°500–2 000 PLN

Reagents, media and consumables

ReagentCASDetails
Sodium chloride NaCl analytical grade7647-14-5Purity ≥99.5%, without iodine addition, Cu content <0.3 ppm, NaI <0.1%, 25 kg
Deionized waterConductivity <20 µS/cm at 25°C, for salt solution preparation
Glacial acetic acid (AASS)64-19-7Purity ≥99.8%, for solution acidification to pH 3.1–3.3
Copper(II) chloride dihydrate (CASS)10125-13-0CuCl₂·2H₂O, concentration 0.26 ± 0.02 g/L in CASS solution
Sodium hydroxide 1 mol/L1310-73-2For pH correction (if too low)
Hydrochloric acid 1 mol/L7647-01-0For pH correction (if too high)

Health and safety (OHS)

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