Filtration System
| Brand | New Biolink |
|---|---|
| Origin | Beijing, China |
| Manufacturer Type | Authorized Distributor |
| Country of Origin | China |
| Model | Filtration System |
| Sample Processing | Waste Water Treatment |
| Filter Types Supported | Activated Carbon Filter, Catalyst Filter, Bag Filter, High-Voltage Insulating Oil Filter, Depth Filter, Sterile Filter, Corrosion-Resistant Filter |
Overview
The New Biolink Filtration System is an engineered modular platform designed for reliable, scalable, and standards-compliant liquid purification in laboratory, pilot-scale, and industrial support environments. It operates on the principle of physical separation—utilizing differential pore size, adsorption (e.g., activated carbon), depth retention, or surface capture—to remove suspended solids, colloids, organic contaminants, catalyst residues, and microorganisms from aqueous waste streams. Unlike single-purpose benchtop units, this system integrates configurable filter housings, pressure-rated manifolds, and standardized flange interfaces (compatible with DIN 2501, ASME B16.5, and GB/T 9113), enabling seamless integration into existing lab wastewater collection loops or closed-loop recycling circuits. Its architecture supports both batch and semi-continuous operation, with maximum working pressure rated per component specification (typically up to 10 bar for stainless steel housings), and temperature tolerance aligned with standard EPDM or PTFE seal options.
Key Features
- Modular filter housing design accommodating industry-standard cartridges, bags, and depth media—enabling rapid reconfiguration for varying contaminant profiles (e.g., switching from coarse particulate removal to sterile-grade filtration).
- Corrosion-resistant construction using 304 or optional 316L stainless steel housings, validated for compatibility with acidic, alkaline, and solvent-laden waste streams per ASTM A240 and ISO 15156-3 guidelines.
- Integrated pressure monitoring ports and differential pressure gauges (0–10 bar range) to track filter loading and optimize maintenance intervals in accordance with ISO 4406 and ISO 16889 particle counting protocols.
- OEM-certified manufacturing traceability: All filter elements are produced under a documented quality management system compliant with ISO 9001:2015, with full material certifications (MTRs), dimensional inspection reports, and functional test records available upon request.
- Standardized mounting interfaces (DIN 2501 flanges, ISO 228 threads) ensure mechanical and sealing interoperability with third-party pumps, flow meters, and control valves commonly deployed in GLP-aligned lab infrastructure.
Sample Compatibility & Compliance
This filtration platform is validated for use with non-hazardous and low-to-moderate hazard aqueous effluents generated during chemical synthesis, bioprocessing, catalyst recovery, and analytical sample preparation. It accommodates feed streams with turbidity up to 500 NTU, total suspended solids (TSS) ≤ 500 mg/L, and pH ranges from 2.0 to 12.0—subject to selected filter media and gasket material compatibility. The system conforms to key international design and safety references: ASME BPVC Section VIII Div. 1 for pressure boundary components; GB/T 14472 (China National Standard) for electrical safety in auxiliary control panels; and ISO 14644-1 Class 8 cleanroom-compatible assembly practices for sterile filtration configurations. While not certified as medical device-grade (ISO 13485), its sterile filter modules meet ISO 13408-1 requirements for bacterial retention (≥ log 7 reduction of Brevundimonas diminuta) when operated within specified flow and pressure parameters.
Software & Data Management
The Filtration System operates as a hardware-integrated unit without embedded firmware or proprietary software. However, it is fully compatible with third-party SCADA and LIMS platforms via analog 4–20 mA pressure and flow output signals (optional transducer integration). All OEM documentation—including filter element specifications, validation protocols (e.g., integrity test procedures per ASTM F838), and maintenance logs—adheres to ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, Available) for audit readiness. For GMP-regulated labs, New Biolink provides customizable IQ/OQ documentation packages supporting FDA 21 CFR Part 11 compliance when paired with validated electronic record systems.
Applications
- Post-synthesis wastewater polishing prior to municipal discharge or on-site reuse.
- Catalyst recovery and recycle loops in homogeneous catalysis workflows.
- Pre-filtration for reverse osmosis or ion exchange systems in lab water purification trains.
- Removal of mycelial debris or cell lysates in upstream bioprocessing support labs.
- Conditioning of insulating oil used in high-voltage testing equipment (per IEC 60296 and ASTM D877).
- Dechlorination and VOC abatement in environmental analysis lab exhaust scrubber effluents.
FAQ
Is this system suitable for filtering organic solvents?
Yes—when configured with fluoropolymer-sealed housings and chemically resistant filter media (e.g., PTFE membranes or activated carbon with solvent-stable binder), subject to compatibility verification using the provided chemical resistance chart.
Can I validate filter integrity in-house?
Absolutely. All sterile and hydrophobic filters supplied with this system support standard forward-flow, bubble point, and diffusion tests per ASTM F838 and EU Annex 1 guidelines.
Does New Biolink provide installation support or commissioning services?
Yes—authorized distributors offer site-specific piping layout review, pressure decay testing, and operator training aligned with ISO/IEC 17025 competency requirements.
Are replacement filter elements traceable to lot-specific test data?
Yes—each batch carries a Certificate of Conformance including particulate challenge results, extractables profile, and endotoxin levels (where applicable).
