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HHitech Pilot-1600 Integrated Ultra-Pure Water System

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Brand HHitech
Origin Shanghai, China
Manufacturer Type Direct Manufacturer
Model Pilot-1600
Pure Water Grade Type I (ASTM D1193-20)
Resistivity 18.2 MΩ·cm at 25°C
Heavy Metals & Soluble Silica <0.01 ppb
Total Organic Carbon (TOC) <3 ppb
Microbial Count <0.01 CFU/mL
Endotoxin <0.001 EU/mL
Particles (>0.1 � m): <1 particle/mL
RO Output Capacity 250 L/h at 25°C
Footprint 0.5 m²
Power Supply 220 VAC, 50 Hz, 480 W
Safety Voltage DC24V control circuitry (<DC36V safety threshold)
RO Membrane Dual independent 800 GPD Dow FilmTec™ ultra-low-pressure elements (operating pressure <70 psi / 4.9 bar)
UV System Dual-wavelength (185 nm & 254 nm) germicidal lamp (imported quartz sleeve)
UF Module MWCO 5000 Da polyethersulfone (PES) ultrafilter
Final Filtration 0.2 μm PES terminal filter
Storage Integrated dual 15 L NSF-certified pressurized tanks
Compliance GLP-compliant architecture, NSF/ANSI Standard 58 & 61 certified tubing and fittings
Data Logging Optional RS232/USB interface with 1-year timestamped audit trail (21 CFR Part 11–ready configuration available)

Overview

The HHitech Pilot-1600 is an integrated, floor-standing ultra-pure water system engineered for centralized laboratory supply and mid-scale process applications requiring continuous, high-reliability Type I water per ASTM D1193-20 and ISO 3696 Class 1 specifications. It employs a multi-stage purification architecture combining prefiltration, dual parallel ultra-low-pressure reverse osmosis (RO), dual-wavelength ultraviolet photo-oxidation, ultrafiltration (UF), and nuclear-grade ion exchange to achieve consistent 18.2 MΩ·cm resistivity, <3 ppb TOC, <0.001 EU/mL endotoxin, and <0.01 CFU/mL microbial content. Unlike conventional high-pressure RO systems operating above 225 psi — which introduce mechanical stress, energy inefficiency, and electrical safety concerns — the Pilot-1600 utilizes two independent 800 GPD Dow FilmTec™ RO modules rated for <70 psi operation, enabling DC24V low-voltage control logic that complies with IEC 61000-1-2 safety thresholds. Its compact 0.5 m² footprint supports dense lab layouts while maintaining full service accessibility and modular expandability — including optional external distribution loops for building-wide feed.

Key Features

  • Dual-redundant ultra-low-pressure RO architecture: Two physically isolated 800 GPD Dow FilmTec™ membrane assemblies operate in parallel; if one fails, the other maintains >50% nominal output (≥125 L/h) without system shutdown.
  • GLP-embedded microprocessor control: Full-color backlit LCD (240×128 pixels) with real-time animated flow-path visualization and multilevel password protection (factory + user tiers).
  • Triple-point online water quality monitoring: Simultaneous resistivity, TOC, and endotoxin-capable sensors track feedwater, RO permeate, and final UP water — all with configurable alarm thresholds and automatic data logging.
  • Intelligent consumables management: Predictive lifetime modeling for prefilter, RO membranes, UV lamps, UF cartridges, and mixed-bed resin columns — with remaining service time displayed and auto-notifications triggered at ≥90% utilization.
  • NSF/ANSI 58 & 61 certified fluid path: All wetted materials — including PES ultrafilters, 0.2 μm terminal filters, and pressurized storage tanks — meet North American potable water safety standards.
  • Modular scalability: Internal cavity预留 space accommodates recirculation pumps, UV recirculation loops, or integration with external 100–1000 L reservoirs for extended batch delivery or central plant interfacing.

Sample Compatibility & Compliance

The Pilot-1600 delivers water suitable for critical analytical, biopharmaceutical, and cell culture workflows where trace contaminants compromise assay integrity. Its <0.001 EU/mL endotoxin level — achieved via MWCO 5000 Da PES ultrafiltration — meets USP and EP 2.6.14 requirements for parenteral-grade water used in IVF, monoclonal antibody production, and primary neuronal culture. The <3 ppb TOC specification (with dual-wavelength UV) satisfies ASTM D5127-21 for HPLC mobile phase preparation and ICH Q5C stability testing. All electronic logging functions support 21 CFR Part 11 compliance when configured with audit-trail-enabled firmware and role-based access controls. System design adheres to ISO 14644-1 Class 8 cleanroom-compatible housing standards, and stainless steel powder-coated chassis ensures corrosion resistance under routine disinfection protocols.

Software & Data Management

The embedded control firmware records timestamped conductivity, TOC, UV intensity, pressure differentials, and consumables status continuously for up to 12 months. Data export is supported via optional RS232 or USB interfaces in CSV format — compatible with LIMS platforms such as LabWare, STARLIMS, and Thermo Fisher SampleManager. Audit trails include operator ID, parameter changes, alarm events, and maintenance logs — all cryptographically signed and immutable post-generation. Firmware updates are performed via secure authenticated channels; configuration backups can be exported to external drives for disaster recovery. Remote diagnostics capability enables OEM-assisted troubleshooting without physical access.

Applications

  • High-performance liquid chromatography (HPLC), UHPLC, and LC-MS mobile phase and blank preparation.
  • Cell culture media formulation, stem cell expansion, and embryology-grade water for assisted reproductive technologies.
  • Atomic absorption spectroscopy (AAS), inductively coupled plasma mass spectrometry (ICP-MS), and trace metal analysis requiring sub-ppt contaminant levels.
  • Pharmaceutical QC testing per USP , EP 2.2.43, and JP 17 standards for Water for Injection (WFI)-adjacent purity.
  • Genomics applications including next-generation sequencing (NGS) library prep and qPCR master mix dilution.
  • Centralized feed for multiple benchtop instruments across core facilities or GMP pilot labs.

FAQ

What is the minimum feedwater quality required for stable 18.2 MΩ·cm output?
Feedwater must meet municipal potable standards per WHO guidelines: TDS ≤200 ppm, temperature 5–45°C, pressure 1.0–4.0 kgf/cm². For TDS >200 ppm, external softening or antiscalant dosing is recommended to prevent RO scaling.
Can the Pilot-1600 be validated per IQ/OQ/PQ protocols?
Yes — full validation documentation packages (including test scripts, acceptance criteria, and raw data templates) are provided. Installation Qualification covers electrical, plumbing, and environmental checks; Operational Qualification verifies alarm response, sensor accuracy, and flow calibration; Performance Qualification confirms sustained 18.2 MΩ·cm, <3 ppb TOC, and <0.001 EU/mL over 72-hour challenge testing.
Is the system compatible with third-party water distribution loops?
Yes — the internal loop interface supports connection to external stainless steel or PVDF recirculation manifolds. Optional booster pump kits and loop-mounted UV reactors are available for closed-loop installations.
How often must the ultrafiltration cartridge be replaced?
Under typical lab usage (200 L/day), the MWCO 5000 Da PES UF module requires replacement every 6–12 months, depending on feedwater endotoxin load. The system tracks cumulative flow and triggers alerts at 90% of rated throughput (10,000 L).
Does the Pilot-1600 support remote monitoring via Ethernet or Wi-Fi?
Standard configuration includes RS232/USB only. Ethernet or Wi-Fi connectivity is available as a factory-installed option with Modbus TCP or HTTP API support for integration into building management systems (BMS) or enterprise SCADA networks.

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