Technical Resources

Hydrogen Evolution Control in Hot-Dip Galvanized Rebar: Maintaining Bond Strength in Concrete

3.15.2021
7 minutes
Scientific illustration showing colorful nanoparticles on a blue structured surface with floating bubbles, representing chemical reactions

Hot-dip galvanized reinforcing steel provides superior corrosion resistance in concrete applications, extending structure service life in chloride-contaminated environments. However, the initial electrochemical reaction between fresh zinc coating and alkaline concrete generates hydrogen gas at the steel-concrete interface, potentially compromising bond strength if left uncontrolled. Fortunately, well-established mitigation methods—chromate passivation treatments or adequate chromate content in cement—reliably suppress this reaction, ensuring galvanized rebar achieves bond strength equal to or exceeding both black steel and epoxy-coated alternatives.

The Zinc-Concrete Interface Reaction

When freshly galvanized rebar contacts wet concrete during placement, the zinc coating encounters a highly alkaline environment (pH typically 12.5-13.5) created by calcium hydroxide and alkali hydroxides in the cement paste. Under these conditions, zinc reacts to form a protective surface layer.

Primary reaction: Zinc + Calcium hydroxide (from concrete) → Calcium hydroxyzincate + Hydrogen gas

Chemical representation: Zn + Ca(OH)₂ + H₂O → CaZn₂(OH)₆·2H₂O + H₂↑

This reaction serves a protective function—calcium hydroxyzincate forms a stable, adherent barrier layer that passivates the zinc surface and prevents further corrosion. However, the concurrent hydrogen gas evolution creates concerns during concrete curing.

Hydrogen Evolution: Bond Strength Implications

Hydrogen gas generated at the rebar-concrete interface can accumulate in microscopic voids and interstices between the zinc coating and surrounding cement paste. This gas accumulation potentially reduces mechanical interlock and adhesion between rebar and concrete, diminishing bond strength below design requirements.

Potential consequences of uncontrolled hydrogen evolution:

  • Reduced pull-out resistance in tension members
  • Diminished development length effectiveness
  • Compromised load transfer from concrete to reinforcement
  • Non-compliance with structural design assumptions

The severity of bond strength reduction depends on:

  • Rate of hydrogen evolution (influenced by concrete alkalinity and temperature)
  • Duration of gas generation before concrete sets
  • Concrete mix characteristics and permeability
  • Rebar surface condition and deformation pattern

Effective Mitigation: Two Proven Methods

Decades of field experience and laboratory research demonstrate that controlling the zinc-concrete reaction through either surface passivation or cement chemistry modification reliably prevents bond strength degradation. When properly mitigated, galvanized rebar bond strength equals or exceeds black steel performance and significantly surpasses epoxy-coated rebar bond strength.

Method 1: Chromate Passivation Treatment

Chromate conversion coatings applied immediately after hot-dip galvanizing create a thin, chemically stable surface layer that moderates zinc reactivity during the critical concrete curing period.

Mechanism and Function

Chromate passivation forms a protective film—typically hexavalent chromium compounds—that:

  • Slows zinc dissolution in alkaline concrete
  • Reduces hydrogen evolution rate
  • Allows concrete to achieve initial set before significant gas generation
  • Gradually depletes during the curing period, allowing normal zinc passivation afterward

The coating does not prevent calcium hydroxyzincate formation entirely; rather, it delays and moderates the reaction until concrete develops sufficient strength and density to accommodate minimal gas generation without bond degradation.

Standard Requirements

ASTM A767/A767M (Standard Specification for Zinc-Coated [Galvanized] Steel Bars for Concrete Reinforcement) and ASTM A1094/A1094M (Standard Specification for Continuous Hot-Dip Galvanized Steel Bars for Concrete Reinforcement) require chromate passivation unless specifically waived by the purchaser.

This mandatory treatment reflects industry consensus that passivation represents the most reliable method for ensuring predictable bond performance across diverse concrete mix designs and placement conditions.

Passivation Coating Longevity

Research conducted by the American Galvanizers Association quantifies chromate passivation coating durability under typical storage and handling conditions:

Measured service life:

  • Minimum duration: 45 days (6.5 weeks)
  • Maximum duration: 98 days (over 3 months)
  • Typical performance: 60-75 days

Coating longevity depends on:

  • Storage environment (humidity, temperature, precipitation exposure)
  • Handling frequency and method
  • Atmospheric contamination levels
  • Rebar bundle configuration affecting drainage and air circulation

Application Timing Considerations

The finite durability of chromate passivation requires coordination between galvanizing, delivery, and concrete placement schedules.

Best practices for passivated rebar:

  • Ideal placement timeline: Within 4-8 weeks of galvanizing
  • Maximum recommended delay: 12 weeks if properly stored
  • Extended storage: Re-test for passivation presence; consider cement chromate addition if coating has degraded

For projects with uncertain placement schedules or extended site storage periods, specifiers should evaluate whether chromate passivation or cement chemistry control better suits project logistics.

Verifying Passivation Coating Presence

ASTM B201 (Standard Practice for Testing Chromate Coatings on Zinc and Cadmium Surfaces) provides standardized methodology for confirming passivation coating integrity.

Test procedure summary:

  1. Apply test reagent to cleaned zinc surface
  2. Observe color development indicating chromate presence
  3. Compare color intensity to standard references
  4. Document coating condition for quality records

Testing before concrete placement verifies adequate protection remains present, particularly for rebar stored outdoors or in humid environments where passivation degradation accelerates.

When to test:

  • Rebar stored longer than 60 days post-galvanizing
  • Visual evidence of surface staining or discoloration
  • Project specifications requiring passivation verification
  • Concerns about storage condition adequacy
  • Using rebar from inventory with unknown galvanizing date

Method 2: Adequate Chromate Content in Cement Mixture

An alternative approach controls hydrogen evolution through chromate compounds naturally present or intentionally added to the concrete mix itself. Sufficient chromate concentration in the alkaline cement paste moderates zinc reactivity without requiring surface passivation treatments.

Mechanism and Chemistry

Chromate ions dissolved in concrete pore solution interact with the zinc surface, forming protective compounds that slow dissolution and hydrogen generation. This chemical inhibition allows concrete to achieve initial set and develop structural matrix before significant gas evolution compromises bond.

Unlike surface passivation that functions temporarily during early curing, cement-distributed chromates remain available throughout the hydration process, providing extended reaction control.

Natural Chromate Levels in Domestic Cement

Most cement produced in North America contains naturally occurring chromium compounds from raw materials (limestone, clay, iron ore, gypsum) and manufacturing processes.

Typical chromate concentrations in North American cement:

  • Range: 20-30 ppm total chromate in final concrete mix
  • Source: Chromium naturally present in cement clinker and supplementary cementitious materials
  • Adequacy: Sufficient for controlling zinc reactions in most applications

This natural chromate content explains widespread successful performance of galvanized rebar in North American precast and cast-in-place concrete—even when chromate passivation coatings are waived or have weathered away during storage.

International Cement Variations

Cement sourced from international suppliers, particularly from regions with stringent environmental restrictions on chromium content, may contain minimal or zero chromates.

Regions with low-chromate cement:

  • European Union (chromium reduction initiatives)
  • Certain Asian markets with environmental regulations
  • Suppliers specifically marketing "chromium-free" cement

When using international cement or domestic suppliers replicating low-chromate formulations, hydrogen evolution control requires either:

  • Maintaining chromate passivation on rebar until placement
  • Intentionally adding chromate compounds to achieve adequate concentration

Target Chromate Concentrations

When cement naturally lacks sufficient chromates or confirmation testing indicates low levels, supplemental addition achieves reliable hydrogen control.

Recommended chromate levels in cement paste:

  • Minimum acceptable: 50 ppm total chromate
  • Optimal range: 100+ ppm total chromate
  • Typical specification: 50-100 ppm (widely successful)

Higher concentrations provide greater safety margin but offer diminishing benefit beyond 100-150 ppm.

Chromate Addition Methods

Common chromate sources for concrete:

  • Sodium chromate (Na₂CrO₄): Water-soluble powder; easily dispersed in mix water
  • Calcium chromate (CaCrO₄): Alternative chromate salt
  • Dilute chromic acid (H₂CrO₄): Liquid addition; requires careful handling

Addition procedure:

  1. Calculate required chromate mass based on cement content and target concentration
  2. Dissolve chromate compound in mix water or add as dry admixture
  3. Ensure thorough distribution during concrete mixing
  4. Document addition rate and final concentration for quality records

Safety considerations: Hexavalent chromium compounds require appropriate handling protocols, personal protective equipment, and environmental controls per OSHA and EPA regulations.

Pre-Testing Cement Chromate Content

Proactive testing eliminates uncertainty about natural chromate levels in cement, enabling informed decisions about supplemental addition necessity.

Testing methodology:

  • Obtain representative cement samples from supplier
  • Chemical analysis quantifies total chromate concentration
  • Compare results against 20-30 ppm baseline for North American cement
  • Document findings for specification compliance and quality assurance

When testing is recommended:

  • First use of a new cement supplier
  • International cement sources
  • Suppliers advertising environmental certifications that may indicate chromate reduction
  • Projects specifying galvanized rebar without passivation
  • Precast operations establishing quality control protocols

Waiving Chromate Passivation Requirements

Both ASTM A767 and A1094 allow purchasers to waive the mandatory chromate passivation requirement when adequate chromate content in cement is verified.

Typical waiver scenarios:

  • Precast concrete operations with established cement chemistry control
  • Projects using proven domestic cement with documented adequate chromate levels
  • Applications where environmental regulations prohibit chromate surface treatments
  • Long-term storage anticipated before concrete placement (passivation would degrade)

Waiver best practices:

  • Document cement supplier chromate content verification
  • Specify minimum acceptable chromate concentration in concrete specifications
  • Establish testing protocols for incoming cement shipments
  • Maintain quality records demonstrating adequate inhibitor presence

Method Selection Criteria

Choosing between chromate passivation and cement chemistry control depends on project-specific factors:

Chromate Passivation (Method 1) Preferred When:

  • Short timeline between galvanizing and placement (< 8 weeks)
  • Cement supplier or chromate content unknown at specification time
  • ASTM A767/A1094 compliance required without waiver
  • Multiple cement suppliers possible during construction
  • Simplicity and universal applicability valued over cement testing
  • Field conditions prevent reliable cement chemistry control

Cement Chromate Control (Method 2) Preferred When:

  • Chromate passivation degraded from extended storage (> 12 weeks)
  • Environmental regulations restrict chromate surface treatments
  • Precast operations with consistent, controlled cement sources
  • International cement documented to lack natural chromates
  • Specification explicitly waives passivation per ASTM A767/A1094
  • ASTM A123 galvanizing of rebar fabrications (passivation not standardized)

Combined Approach

Maximum assurance results from employing both methods:

  • Specify chromate passivation per ASTM A767/A1094
  • Verify adequate cement chromate content as backup protection
  • Provides redundancy if passivation degrades during storage

This conservative approach suits critical infrastructure, marine exposure structures, and projects where bond strength verification testing is impractical.

Bond Strength Performance Data

When hydrogen evolution is properly controlled through either method, galvanized rebar demonstrates excellent bond performance:

Comparative bond strength (properly mitigated galvanized rebar):

  • Equal to or greater than black steel rebar
  • Significantly exceeds epoxy-coated rebar bond strength
  • Meets or surpasses design assumptions in ACI 318 development length calculations

Research documenting this performance includes studies by:

  • American Galvanizers Association field trials
  • Federal Highway Administration corrosion research
  • Academic institutions conducting pull-out and beam tests
  • International precast concrete associations

The zinc coating's rough, crystalline surface texture—particularly the characteristic "spangle" pattern—provides excellent mechanical interlock with concrete once hydrogen evolution is controlled.

Practical Implementation Guidelines

For Specifiers and Engineers:

When specifying galvanized rebar:

  1. Default to ASTM A767 or A1094 with chromate passivation unless concrete chemistry is confirmed adequate
  2. If waiving passivation, explicitly specify minimum cement chromate content (50-100 ppm recommended)
  3. Require cement testing documentation from concrete supplier
  4. Consider placement timeline when evaluating passivation necessity
  5. Document rationale for method selection in project specifications

For Contractors and Rebar Fabricators:

Quality control procedures:

  1. Verify passivation coating presence if storage exceeds 60 days (ASTM B201 testing)
  2. Coordinate galvanizing schedule with anticipated placement timeline
  3. Store passivated rebar to minimize moisture exposure and coating degradation
  4. Communicate storage duration to concrete supplier if cement chromate addition may be needed
  5. Document galvanizing date and passivation application for traceability

For Concrete Suppliers:

Mix design considerations:

  1. Test cement chromate content, especially if using non-traditional sources
  2. Maintain documentation of natural chromate levels for customer verification
  3. Establish chromate addition protocols if supplementation becomes necessary
  4. Communicate cement chemistry to contractors placing galvanized rebar
  5. Consider standardizing adequate chromate content across all mixes for operational simplicity

Environmental and Regulatory Considerations

Hexavalent chromium compounds used in passivation treatments and cement additions face increasing regulatory scrutiny due to environmental and health concerns.

Current regulatory landscape:

  • Chromate passivation remains permitted in most jurisdictions for industrial applications
  • Proper handling, storage, and disposal protocols required per OSHA and EPA
  • Some regions restricting chromate use in consumer products (not affecting rebar applications)
  • Industry research ongoing into alternative hydrogen evolution inhibitors

Future outlook: Research continues into non-chromate alternatives including:

  • Trivalent chromium compounds (lower toxicity)
  • Organic corrosion inhibitors
  • Modified zinc bath chemistry reducing alkaline reactivity
  • Concrete admixtures providing alternative hydrogen control

Until alternatives achieve equivalent proven performance, chromate-based methods remain industry standard for ensuring reliable bond strength in galvanized rebar applications.

Hydrogen evolution at the zinc-concrete interface represents a manageable phenomenon with well-established mitigation strategies. Chromate passivation treatments applied immediately after hot-dip galvanizing provide reliable hydrogen control for projects with predictable placement schedules, while adequate chromate content in cement offers robust protection for precast operations and situations where surface treatments are impractical. Both methods deliver equivalent outcomes: galvanized rebar bond strength equal to or exceeding black steel performance while providing the superior corrosion protection that extends concrete structure service life in aggressive chloride environments. Proper method selection based on project logistics, cement chemistry verification, and coordination between galvanizers, concrete suppliers, and contractors ensures galvanized reinforcing steel achieves its full potential for maintenance-free, long-term structural performance. Learn more at the original AGA resource on Hydrogen Evolution Control in HDG Rebar.

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