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TQC C&W Corrosion Test Chamber

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Origin Netherlands
Manufacturer Type Authorized Distributor
Origin Category Imported
Model C&W
Spray Method Air-Atomized Nozzle System
Fog Deposition Rate 1.0–2.0 mL/80 cm²/h (adjustable per ASTM B117 & ISO 9227)
Nozzle Pressure 0.7–1.0 bar (regulated)
De-misting Method Compressed Air Blow-Off + Thermal Drying Cycle
Temperature Range Ambient to 50 °C (±0.5 °C uniformity)
Humidity Control Range 10–98% RH (±2% RH accuracy)
Chamber Capacities 100 L, 200 L, 450 L, 750 L

Overview

The TQC C&W Corrosion Test Chamber is an engineered environmental test system designed for accelerated corrosion evaluation of metallic substrates, protective coatings, and finished components under standardized salt spray, cyclic humidity, and combined climate stress conditions. Based on the fundamental principles of electrochemical corrosion acceleration—where controlled chloride ion exposure, temperature elevation, and humidity cycling simulate decades of real-world degradation in weeks—the C&W chamber delivers repeatable, traceable, and auditable test environments compliant with internationally recognized protocols including ASTM B117 (neutral salt spray), ASTM G85 (modified salt spray cycles), ISO 9227, ISO 16701 (cyclic corrosion testing), and VDA 621-415 (automotive cyclic tests). Its modular architecture supports both static salt fog exposure and dynamic multi-phase test sequences—including dry-off, humid soak, salt spray, and condensation phases—enabling laboratories to replicate service-life environmental profiles across automotive, aerospace, marine, electronics, and industrial coating applications.

Key Features

  • Robust stainless steel 316L chamber construction with reinforced insulation and double-wall design for thermal stability and long-term chemical resistance
  • Precision-engineered air-atomized spray nozzles with pressure-regulated delivery (0.7–1.0 bar), ensuring uniform fog distribution and compliance with ASTM B117 fog deposition specifications (1.0–2.0 mL/80 cm²/h)
  • Integrated de-misting system combining compressed-air blow-off and programmable thermal drying cycles to prevent residual salt carryover between test phases
  • Independent high-accuracy temperature control (ambient to 50 °C, ±0.5 °C uniformity) and humidity regulation (10–98% RH, ±2% RH accuracy) via PID-controlled steam humidification and refrigerated dehumidification
  • Four standard chamber volumes (100 L, 200 L, 450 L, 750 L) with fully documented internal dimensions, all validated for spatial uniformity per IEC 60068-3-5 and ISO 16701 Annex A
  • Front-access door with magnetic seal and viewing window; removable sample racks with adjustable spacing for flexible fixture configuration

Sample Compatibility & Compliance

The C&W chamber accommodates flat test panels (up to 150 × 70 mm), cylindrical specimens, assembled subassemblies, and coated fasteners without requiring custom tooling. All models meet CE marking requirements and are designed for integration into GLP- and GMP-compliant quality systems. Test data generated using this chamber satisfies regulatory expectations for material qualification under ISO/IEC 17025-accredited laboratories. The system supports full traceability through configurable audit trails, user access levels, and electronic signature capability—aligning with FDA 21 CFR Part 11 requirements when paired with validated software configurations. Calibration certificates for temperature, humidity, and fog deposition rate are provided with each unit and conform to ISO/IEC 17025 calibration intervals.

Software & Data Management

The C&W chamber operates via a dedicated touchscreen HMI with embedded controller firmware supporting up to 99 programmable test cycles, each comprising up to 100 individual steps (spray, dry, humid, condense, rest). Real-time logging records temperature, relative humidity, spray status, and elapsed time at user-defined intervals (minimum 1-minute resolution). Exportable CSV logs include timestamps, setpoints, actual readings, and alarm events. Optional PC-based software enables remote monitoring, report generation (PDF/Excel), deviation alerts, and integration with LIMS platforms via Modbus TCP or OPC UA. All software modules undergo version-controlled validation documentation per IQ/OQ protocols.

Applications

  • Automotive OEMs and Tier-1 suppliers validating paint systems, galvanized steel, aluminum alloys, and brake components per VDA 621-415 and GMW14872
  • Coating manufacturers assessing primer-surfacer-topcoat performance under ISO 12944 C5-I/C5-M severity classes
  • Aerospace component testing per ASTM D1654 and SAE AMS 2700 for corrosion resistance of fasteners, housings, and composite substrates
  • Electronics enclosure qualification under IEC 60068-2-11 (salt mist) and IEC 60068-2-30 (damp heat cycling)
  • Marine and offshore equipment certification per ISO 20340 and NORSOK M-501
  • Academic and industrial R&D labs conducting comparative corrosion kinetics studies and inhibitor efficacy screening

FAQ

What standards does the C&W chamber support out-of-the-box?
ASTM B117, ASTM G85 Annex A1–A5, ISO 9227, ISO 16701, VDA 621-415, and DIN 50021—all supported via preloaded test templates and validated hardware parameters.
Is the fog deposition rate independently verified and adjustable?
Yes. Each chamber undergoes factory verification using standardized collection funnels per ASTM B117 Section 7.2. Rate is continuously adjustable within 1.0–2.0 mL/80 cm²/h via nozzle pressure and solution flow control.
Can the chamber perform fully automated cyclic tests without manual intervention?
Yes. All four chamber sizes support unattended operation of multi-phase cycles (e.g., 4-hr salt spray → 4-hr dry → 4-hr humid soak → 4-hr condensation) for up to 99 consecutive days.
What maintenance is required for long-term reliability?
Routine tasks include weekly distilled water reservoir refill, monthly nozzle inspection/cleaning, quarterly calibration verification, and annual preventive maintenance by TQC-certified service engineers.
Does the system provide audit-ready documentation for ISO 17025 or FDA audits?
Yes. With optional software licensing, the system generates 21 CFR Part 11–compliant electronic records, including user logins, parameter changes, alarm history, and calibration metadata—with immutable timestamps and digital signatures.

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