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PEAK INFINITY XE 5041 Nitrogen Generator for LC-MS

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Brand PEAK
Origin United Kingdom
Manufacturer Type Original Equipment Manufacturer (OEM)
Import Status Imported
Model INFINITY XE 5041
Nitrogen Generation Principle Membrane Separation
Output Flow Rate 40–520 L/min
Output Pressure up to 135 psi
Nitrogen Purity up to 99.5%
Dew Point −40 °C
Inlet Pressure 60–145 psi
Input Voltage 100–230 VAC, 50/60 Hz
Dimensions (H×W×D) 500 × 500 × 995 mm

Overview

The PEAK INFINITY XE 5041 Nitrogen Generator is an engineered solution designed specifically to supply high-purity nitrogen gas to multiple liquid chromatography–mass spectrometry (LC-MS) systems within centralized laboratory environments. Utilizing proprietary hollow-fiber membrane separation technology, the system selectively permeates oxygen, water vapor, and other trace gases from compressed air feedstock—leaving behind a continuous stream of nitrogen with consistent purity up to 99.5% (v/v). Unlike pressure swing adsorption (PSA) systems, membrane-based generation operates without moving parts, eliminating mechanical wear, vibration, or audible operational noise. This architecture ensures long-term reliability, stable output under variable demand, and compliance with the stringent gas quality requirements of modern electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) sources. The INFINITY XE 5041 is intended for integration into laboratories that already maintain a clean, dry compressed air supply meeting ISO 8573-1:2010 Class 1.4.1 specifications (i.e., ≤0.1 µm particles, ≤0.01 mg/m³ oil content, dew point ≤−70 °C at pressure).

Key Features

  • Continuous nitrogen output across a wide flow range: 40–520 L/min—scalable to support two or more LC-MS instruments simultaneously without flow interruption or pressure drop.
  • Stable outlet pressure up to 135 psi (9.3 bar), compatible with standard LC-MS pneumatic interfaces and auxiliary gas modules (e.g., nebulizer, drying, and sheath gas lines).
  • Consistent nitrogen purity of ≥99.5% (v/v) at full rated flow, verified via on-board electrochemical sensor monitoring and traceable calibration protocols.
  • Dew point control to −40 °C (at atmospheric pressure), ensuring minimal moisture ingress into sensitive ion source components and reducing risk of oxidation or signal drift.
  • Zero-maintenance core design: no valves, compressors, or desiccant beds—only periodic inspection of inlet filtration and membrane integrity per manufacturer-recommended intervals.
  • Compact footprint (500 × 500 × 995 mm) optimized for placement in equipment rooms or adjacent to instrument racks; rear-access service layout simplifies utility routing.

Sample Compatibility & Compliance

The INFINITY XE 5041 does not process samples directly but serves as a critical utility subsystem for analytical instrumentation requiring inert, low-humidity carrier and auxiliary gases. It complies with ISO 8573-1:2010 Class 1.4.1 for inlet air quality and delivers output gas meeting ASTM D6352-22 (Standard Specification for Nitrogen Used in Analytical Instrumentation) for purity and moisture limits. When integrated into regulated environments—including those operating under GLP, GMP, or FDA 21 CFR Part 11 frameworks—the generator supports audit-ready documentation through optional digital I/O and Modbus RTU interface for remote status logging and alarm integration. PEAK provides factory-issued certificates of conformance, material declarations (RoHS/REACH), and validation support packages for IQ/OQ execution.

Software & Data Management

While the INFINITY XE 5041 operates autonomously without embedded firmware or touchscreen UI, it includes analog and digital outputs for real-time monitoring of key parameters: outlet pressure, flow rate, and nitrogen purity (via optional sensor module). Integration with laboratory building management systems (BMS) or centralized gas monitoring platforms is enabled via 4–20 mA analog signals and Modbus RTU over RS-485. PEAK supplies configuration templates and register maps for seamless incorporation into SCADA or LIMS environments. All operational data—including runtime hours, filter service alerts, and pressure deviation logs—can be archived externally for trend analysis, preventive maintenance scheduling, and regulatory review.

Applications

  • Primary nitrogen supply for multi-instrument LC-MS laboratories performing quantitative bioanalysis, metabolomics, proteomics, and environmental residue testing.
  • Auxiliary gas source for APCI and ESI ion sources, including nebulizing, drying, and curtain gas functions where consistent dew point and hydrocarbon-free composition are essential.
  • Carrier gas for GC-MS systems requiring non-reactive, low-moisture nitrogen—particularly in trace-level pesticide or volatile organic compound (VOC) analysis.
  • Blanketing and purging applications in sample preparation workflows involving light-sensitive or oxidation-prone analytes (e.g., lipidomics, redox metabolite profiling).
  • Support infrastructure for automated sample introduction systems (e.g., robotic autosamplers) requiring stable pneumatic actuation pressure.

FAQ

What compressed air quality is required for optimal performance?
The INFINITY XE 5041 requires inlet air compliant with ISO 8573-1:2010 Class 1.4.1: ≤0.1 µm particulates, ≤0.01 mg/m³ total oil content (including aerosol and vapor), and a pressure dew point ≤−70 °C at line pressure.
Can the system operate continuously 24/7?
Yes—designed for unattended, duty-cycle-independent operation with thermal overload protection, pressure relief valves, and fail-safe shut-off logic for inlet/outlet anomalies.
Is external cooling or ventilation required?
No active cooling is needed; ambient airflow around the unit (minimum 10 cm clearance on all sides) is sufficient for passive thermal dissipation.
How often must filters be replaced?
Pre-filtration stages (coalescing + activated carbon) require replacement every 6,000–8,000 operating hours depending on inlet air quality; PEAK provides condition-monitoring indicators and scheduled maintenance alerts via optional digital interface.
Does the system meet FDA 21 CFR Part 11 requirements?
The base unit is Part 11–ready when integrated with validated third-party data acquisition systems; PEAK offers electronic signature-capable validation documentation packages and audit trail configuration guidance upon request.

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