Technical Data & Downloads

Salt Spray Hours

Salt spray testing, also known as salt fog testing or salt spray corrosion testing, is a widely used method for evaluating the corrosion resistance of applied materials and coatings

PASSIVATION OVER 10 µm ZINCHOURS BEFORE WHITE RUSTHOURS BEFORE RED RUST
Hexavalent Blue24-28100-200
Hexavalent Yellow96-175250-500
Hexavalent Green / Olive Drab150-225400-750
Hexavalent Black72-96250-270
TRI-valent EnviroPassTM200-400500-750
MegaZinc®400-600500-900
MegaZinc® Black250300-500

Note:

This is on an average micron thickness of 10um, in a neutral salt spray test to less than 5%


MegaZinc® has 3 different Classes.


See our MegaZinc® page for more information

Environmental Corrosion Rates

Measuring environmental corrosion rates is crucial for assessing the durability and reliability of metallic materials for specific applications

Spec: ISO 9223

CORROSION
CLASS
CATAGORYENVIRONMENT
(INTERIOR)
ENVIRONMENT
(EXTERIOR)
CORROSION
(ZINC)
GUIDE DURABILITY OF CHROMATE
====(Average)(MIN-MAX)
0None0(0-0)um/YEAR
C1insignificant – Very LowHeated buildings with clean atmospheres, such as offices, shops, schools, and hotels=0.5(0-1)um/YEAR
C2LowUnheated buildings where condensation can occur, such as depots, and sports halls.Atmosphere with low level of pollution: mostly rural areas1.5(1-2)um/YEAR
C3MediumProduction rooms with high humidity and some air pollution; such as food processing plants, laundries, breweriesUrban and industrial atmosphere, moderate sulfur dioxide pollution; coastal areas with low salinity3(2-5)um/YEAR
C4HighChemical plants, swimming pools, coastal ships, and boatyards.Industrial areas and coastal areas with moderate salinity==
C5V. HighBuildings or areas with almost permanent condensation with high pollutionIndustrial areas with high humidity and aggressive atmosphere and coastal areas with high salinity==
CXExtremely HighIndustrial areas with extreme humidity and aggressive atmosphereOffshore areas with high salinity industrial areas with extreme humidity and aggressive atmosphere and subtropical and tropical atmospheres==

Understanding environmental corrosion rates helps engineers and materials scientists select appropriate materials, coatings, and corrosion protection strategies to mitigate degradation and ensure the long-term performance of structures, equipment, and components exposed to challenging environmental conditions

ROHS: Max Allowed PPM

ComponentSymbolMax PPM
LeadPb1000
MercuryHg1000
Hexavalent ChromiumCr1000
Polybrominated DiphenylethersPBB1000
Decabromodiphenyl EthersDECA-BDE1000
CadmiumCd100

ROHS, which stands for Restriction of Hazardous Substances, sets limits on the maximum concentration of certain hazardous substances in electrical and electronic equipment.

The maximum concentration is usually measured in parts per million (PPM). For example, under the ROHS directive, certain hazardous substances such as lead (Pb), mercury (Hg), cadmium (Cd), hexavalent chromium (Cr6+), polybrominated biphenyls (PBB), and polybrominated diphenyl ethers (PBDE) must not exceed specified maximum concentrations, typically measured in PPM, in electronic products placed on the market within the European Union (EU).

Typical Rust timeline

Description of StageTypical Visual SignsApproximate Time-frame*Environmental/accelerating factors
Bare ferrous metal (iron or steel) newly exposed or stripped of coating. No major corrosion products yet.Clean steel surface, possibly light surface oxidation film but no visible rust.Hours to daysHigh humidity, salt spray, pollutants, condensation will speed next stage.
If zinc-coated (electroplated or galvanised), zinc reacts with O₂ and CO₂ to form a stable zinc-carbonate/hydroxide patina (especially with wet/dry cycles). (American Galvanizers Association)Zinc coating remains intact; surface may dull to a matte grey as patina forms.Weeks to months (e.g., 1-12 months) depending on environment and coating thicknessFrequent wet/dry cycles (good), ventilation, clean environment help proper patina formation. Trapped moisture, poor ventilation hamper it.
On zinc-coated parts stored or exposed to moisture/poor ventilation, a white‐powdery deposit forms (zinc oxide/hydroxide/carbonate) rather than a dense protective film. (Conklin Metal)Whitish, chalky, waxy deposit on coated parts (especially in overlapping/stacked areas)Days to weeks under adverse conditionsHigh humidity, standing water or droplets trapped between parts, lack of airflow/CO₂, chlorides or pollutants accelerate it. (American Galvanizers Association)
The zinc layer has been consumed or compromised (via white rust, mechanical damage, scratches), base ferrous metal is exposed.Bare steel exposure, small rust spots beginning.Months to years depending on coating thickness & environmentSalt spray, industrial atmosphere, acid/alkali exposure, mechanical damage, micro-galvanic effects.
Iron reacts with water + oxygen to form iron (hydr)oxides (ferric oxide etc.). The familiar red/brown rust that eats into steel. (Engineering-Edge)Reddish-brown flaky rust, loss of material, pitting, surface roughness.Months to many years (depending on environment & coating thickness)Marine atmosphere, high salt content (chlorides), high humidity, acid rain, lack of maintenance all accelerate.
Extensive red rust, loss of section thickness, possible failure of part.Large rust flakes, holes, severe pitting, possible structural failure.Years to decades depending on severitySevere exposures, cyclic loading, neglected maintenance, combined chemical attack (e.g., chlorides + acid) lead to this fastest.

How White Rust Forms vs How Red Rust Forms

White rust:

  • Occurs primarily on zinc‐coated surfaces (galvanised or zinc-plated) when the normal protective zinc patina cannot form properly because of lack of airflow, trapped moisture, and/or insufficient CO₂ access.
  • The white deposit is a porous/gelatinous mixture of zinc hydroxides, oxides and carbonates that does not provide a dense protective barrier the way a proper patina does.
  • Because the coating is compromised, the zinc layer may be consumed quickly, eventually exposing the steel substrate.
  • Prevention: Ensure good ventilation, avoid stacking/trapping moisture, apply passivation and top-coats.

Red rust:

Accelerated by salt (chlorides), acid/alkali environments, high humidity, and mechanical damage to coatings.

Occurs on iron or steel when the protective barrier (zinc coating or paint) is breached and the steel is exposed to moisture and oxygen.

The iron oxidises to iron (III) oxides (ferric oxide etc).

Red rust is destructive — it actually corrodes the base metal, leading to section loss and structural issues.

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