Empowering Scientific Discovery

Drick DRK311 Gas Permeability Analyzer

Add to wishlistAdded to wishlistRemoved from wishlist 0
Add to compare
Brand Drick
Origin Shandong, China
Manufacturer Type Original Equipment Manufacturer (OEM)
Country of Manufacture China
Model DRK311
Price USD 7,000 (FOB Qingdao)
Measurement Principle Constant-Volume/Variable-Pressure (Manometric) Method
Standards Compliance GB/T 1038, ASTM D1434, ISO 2556, ISO 15105-1, JIS K7126-A, YBB 00082003
Test Gases O₂, N₂, CO₂
Permeation Range 0.01–55,000 cm³/(m²·24h·0.1 MPa)
Vacuum Resolution 0.1 Pa
Base Vacuum <10 Pa
Vacuum Capacity 0–1333 Pa
Temperature Range 15–50 °C
Temp. Control Accuracy ±0.05 °C
Test Chambers 3 independent
Sample Size Standard 97 cm² (Ø111 mm)
Power Supply AC 220 V, 50 Hz
Power Consumption <1000 W
Dimensions (W×D×H) 680 × 380 × 280 mm
Net Weight 65 kg
Gas Supply Pressure 0.4–0.6 MPa
Test Pressure Range 0–0.15 MPa

Overview

The Drick DRK311 Gas Permeability Analyzer is a manometric, constant-volume/variable-pressure instrument engineered for precise quantification of gas transmission rates through polymeric films, laminates, and rigid sheet materials. It operates on the fundamental principle of measuring pressure rise in a sealed test chamber resulting from gas permeation across a conditioned specimen under controlled temperature and differential partial pressure. This method—standardized in ISO 15105-1 and ASTM D1434—ensures traceable, reproducible determination of oxygen transmission rate (OTR), nitrogen transmission rate (NTR), carbon dioxide transmission rate (CO₂TR), as well as derived material parameters including diffusion coefficient (D), solubility coefficient (S), and permeability coefficient (P = D × S). Designed for packaging R&D laboratories, quality control departments, and regulatory-compliant production facilities, the DRK311 delivers metrological rigor aligned with global pharmacopoeial and food-contact material requirements.

Key Features

  • Triple independent test chambers enable parallel evaluation of up to three specimens—identical or dissimilar—under identical environmental conditions, improving throughput without compromising inter-chamber isolation.
  • High-stability vacuum transducers (imported, calibrated to NIST-traceable standards) provide 0.1 Pa resolution and sustained base vacuum <10 Pa, minimizing baseline drift and enhancing low-flux measurement fidelity.
  • Patented mechanical sealing architecture—including torque-controlled clamping via dedicated calibration wrench—ensures uniform compressive load (±2% repeatability) across all test heads, eliminating operator-induced variability in gasket deformation and leak path formation.
  • Dual-mode test logic: configurable proportional control and fuzzy-logic-based endpoint detection adapt dynamically to material permeation kinetics, optimizing test duration while maintaining statistical confidence in endpoint determination.
  • Integrated industrial-grade computing platform (embedded x86 motherboard, real-time OS) executes full automation—from vacuum evacuation and degassing cycles to permeation monitoring and data interpolation—without external PC dependency.
  • Proprietary lubricant application system ensures consistent, contamination-free seal interface preparation; eliminates manual grease variability and supports cleanroom-compatible operation per ISO 14644 Class 8 protocols.
  • Modular pneumatic manifold with stainless-steel solenoid valves and PTFE-lined tubing guarantees long-term integrity against gas adsorption/desorption hysteresis, critical for high-accuracy O₂ and CO₂ measurements.

Sample Compatibility & Compliance

The DRK311 accommodates flat, non-porous specimens up to 1 mm thickness, including mono-layer plastics (e.g., PET, PE, PP), metallized films, AlOx/SiOx-coated substrates, pharmaceutical blister lidding, and multilayer barrier laminates. All test fixtures conform to ISO 2556-defined sample mounting geometry (97 cm² effective area, Ø111 mm aperture). The system meets full technical alignment with GB/T 1038–2000, ASTM D1434–2013 (Method A), ISO 15105-1:2007, JIS K7126-A:2019, and YBB 00082003–2015 (Chinese Pharmacopoeia packaging guidance). Its software architecture implements ALCOA+ data integrity principles and satisfies FDA 21 CFR Part 11 requirements for electronic records and signatures—including role-based access control, audit trail logging (immutable timestamped entries), and electronic signature workflows.

Software & Data Management

The embedded analytical suite features a modular, client-server-capable architecture supporting local operation and networked deployment. It includes automated report generation (PDF/CSV/XLSX), customizable templates compliant with GLP/GMP documentation standards, and real-time remote diagnostics via secure TLS-encrypted SSH tunneling. Data export adheres to ASTM E2500-17 guidelines for analytical instrument data interchange. Audit trails record all user actions—including method edits, parameter overrides, and result approvals—with cryptographic hashing to prevent tampering. System validation packages (IQ/OQ/PQ protocols) are available upon request to support regulated environments.

Applications

  • Barrier performance benchmarking of flexible packaging for pharmaceutical blister cards, medical device pouches, and sterile barrier systems.
  • Accelerated shelf-life modeling via Arrhenius-based temperature-dependent permeability analysis (15–50 °C range).
  • Validation of coating efficacy (e.g., SiOₓ, AlOₓ, PVDC) on PET and CPP substrates for food packaging applications.
  • QC release testing of incoming film rolls against contractual OTR specifications per ISO 11607–1:2019.
  • Diffusion-solubility decoupling studies for polymer blend development and nanocomposite barrier optimization.
  • Regulatory submission support for FDA 510(k), CE marking, and PMDA dossier preparation requiring ISO 15105-compliant permeation data.

FAQ

What gases can be tested on the DRK311?
O₂, N₂, and CO₂ are fully supported; other permanent gases (e.g., He, Ar) may be evaluated subject to sensor calibration and gas compatibility verification.
Is the system compliant with 21 CFR Part 11?
Yes—the software implements full electronic signature functionality, audit trail retention (>10 years), and role-based permission tiers meeting FDA requirements for regulated laboratories.
Can test data be exported to LIMS?
Yes, via standardized CSV/XML output and optional OPC UA server integration for seamless LIMS connectivity.
What maintenance is required for long-term accuracy?
Annual recalibration of vacuum sensors and temperature probes is recommended; seal gaskets should be replaced every 12 months or after 500 test cycles.
Does the DRK311 support custom test methods?
Yes—users may define non-standard temperature profiles, pressure ramp rates, and endpoint criteria within the method editor, with version-controlled method archiving.

InstrumentHive
Logo
Compare items
  • Total (0)
Compare
0