Q Pack TIX Ultra-Purification Cartridge
| Brand | Deepflow |
|---|---|
| Origin | Shanghai, China |
| Manufacturer Type | Authorized Distributor |
| Product Origin | Domestic (China) |
| Model | CYTUM0TIX1 |
| Pricing | Available Upon Request |
Overview
The Q Pack TIX Ultra-Purification Cartridge is a high-performance, single-use purification module engineered for integration into laboratory-scale ultra-pure water (UPW) systems. Designed to deliver Type I ultrapure water per ISO 3696:1987 and ASTM D1193-2023 specifications, the cartridge employs a multi-stage purification architecture combining activated carbon pre-filtration, mixed-bed ion exchange resin, and sub-micron final polishing—optimized to reduce total organic carbon (TOC) to <5 ppb, resistivity to ≥18.2 MΩ·cm at 25 °C, and bacterial load to <0.01 CFU/mL. Unlike traditional serviceable columns, the Q Pack TIX utilizes a sealed, factory-validated housing with integrated RFID tag for batch traceability and usage logging—ensuring consistent performance without on-site regeneration or chemical handling. It is intended for use downstream of primary reverse osmosis (RO) or deionization (DI) units in analytical, pharmaceutical, and semiconductor R&D environments where reproducible water quality is critical to assay integrity and instrument longevity.
Key Features
- Factory-precharged, pre-equilibrated mixed-bed resin with ultra-low leachables—certified for ≤0.1 ng/mL sodium, chloride, and silica elution under nominal flow conditions
- Integrated 0.22 µm hydrophilic PES membrane final filter—validated for bacterial retention (≥7-log reduction) and non-pyrogenic performance
- RFID-enabled cartridge identification supporting automated system recognition, usage cycle tracking, and audit-ready lifecycle logging
- Pressure-rated housing (up to 6 bar) with sanitary quick-connect fittings (1/4″ push-to-connect) compliant with ISO 8536-4 and USP material requirements
- Pre-sterilized via gamma irradiation (25–35 kGy); endotoxin level ≤0.001 EU/mL per LAL test (USP )
- Designed for plug-and-play replacement—no resin packing, acid/base regeneration, or validation requalification required between changes
Sample Compatibility & Compliance
The Q Pack TIX is compatible with feed water meeting ASTM D1193 Type II or ISO 3696 Grade 2 specifications (conductivity ≤1.0 µS/cm). It is not intended for direct use with raw tap or well water. The cartridge complies with key regulatory frameworks governing laboratory water quality: ISO 3696:1987 (Water for analytical laboratory use), ASTM D1193-2023 (Standard Specification for Reagent Water), CLSI EP22-A (Evaluation of Water Quality for Clinical Laboratory Use), and supports GLP/GMP water system qualification per Annex 1 (EU) and FDA Guidance for Industry: Sterile Drug Products Produced by Aseptic Processing. All materials of construction—including housing (medical-grade polypropylene), resin matrix (styrene-divinylbenzene copolymer), and membrane (polyethersulfone)—are USP Class VI certified and extractables tested per USP .
Software & Data Management
When deployed within Deepflow’s TIX-integrated UPW platforms (e.g., PureLab Chorus TIX series), the cartridge interfaces with embedded firmware that records installation timestamp, cumulative volume dispensed, pressure differential across the unit, and real-time conductivity/TOC alerts. Data export is supported via USB-C or Ethernet (Modbus TCP) in CSV or XML format. Audit trails meet FDA 21 CFR Part 11 requirements, including electronic signatures, user access controls, and immutable event logs. Optional cloud synchronization enables remote monitoring, predictive replacement scheduling, and automated calibration certificate retrieval tied to individual cartridge serial numbers.
Applications
- HPLC, UHPLC, and LC-MS mobile phase preparation where low TOC and ionic contamination prevent column fouling and baseline drift
- Cell culture media formulation and buffer preparation requiring endotoxin-free, nuclease-free water per ATCC and ECACC guidelines
- ICP-MS and GF-AAS trace metal analysis—minimizing background interference from Na⁺, K⁺, Ca²⁺, Fe³⁺, and Al³⁺
- Semiconductor wafer cleaning and photolithography rinse steps demanding particle counts <1 particle/mL at ≥0.5 µm (per SEMI F57)
- Calibration standard preparation for clinical chemistry analyzers (e.g., Roche Cobas, Siemens Atellica) per CLIA and CAP requirements
FAQ
What is the recommended service life of the Q Pack TIX cartridge?
Cartridge lifetime is flow- and feed-water dependent; typical capacity is 1,200–1,800 L at ≤1.5 L/min with feed conductivity ≤2 µS/cm. System firmware calculates remaining capacity based on real-time resistivity decay and pressure rise.
Can the Q Pack TIX be used in series with other purification modules?
Yes—it is designed for modular cascade configurations, including upstream UV oxidation (254/185 nm) or ozone injection units, provided hydraulic compatibility and pressure drop limits are observed.
Is the RFID tag writable or read-only?
Read-only at time of manufacture; contains immutable lot number, sterilization date, resin batch ID, and expiration date (24 months from production).
Does the cartridge require system recalibration after replacement?
No—factory calibration data is embedded in the RFID; the host system auto-loads performance parameters upon detection.
Are replacement cartridges supplied with full QC documentation?
Yes—each unit ships with a Certificate of Conformance (CoC), Certificate of Sterilization (gamma dose report), and extractables/toxicology summary per ISO 10993-12.
