Empowering Scientific Discovery

Beifen Sanpu LAHS-20A Plus Fully Automated Headspace Sampler

Add to wishlistAdded to wishlistRemoved from wishlist 0
Add to compare
[Brand Beifen Sanpu
Origin Beijing, China
Manufacturer Type Direct Manufacturer
Model LAHS-20A Plus
Sample Positions 20
Heating Range (Sample/Valve/Transfer Line) 40–220 °C (optional to 300 °C)
Temperature Accuracy ±0.5 °C
Temperature Stability < ±0.5 °C
Pressure Control Range 0–0.25 MPa (continuously adjustable)
Quantitative Loop Volume 1 mL (customizable: 0.5/2/5 mL)
Vial Capacity 10 mL or 20 mL (customizable: 50/100 mL)
Sampling Time 0–30 min
Injection Time 0–999 s
Pressurization Time 0–999 s
Purge/Flush Time 0–30 min
Minimum Time Resolution 1 ms
Carrier Gas Flow Control EPC-compatible (optional)
RSD < 1.0% (for 100 ppm ethanol in water)
Interface USB
Sample Path Materials Deactivated fused-silica and high-inertness stainless-steel tubing
Valve Configuration Heated 6-port switching valve with integrated quantitative loop]

Overview

The Beifen Sanpu LAHS-20A Plus Fully Automated Headspace Sampler is an engineered solution for reproducible, unattended volatile organic compound (VOC) analysis in compliance-critical laboratories. Designed around the fundamental principle of equilibrium headspace sampling—where volatile analytes partition between a solid or liquid sample matrix and its overlying gas phase—the LAHS-20A Plus enables precise, pressure-controlled transfer of the equilibrated vapor into a gas chromatograph (GC) without liquid-phase carryover. Its architecture supports both static and pressurized headspace injection, delivering robust performance for environmental testing, pharmaceutical residual solvent analysis (per USP & ICH Q2(R2)), food flavor profiling, forensic toxicology, and polymer outgassing studies. The system operates under ISO/IEC 17025-aligned workflows and integrates seamlessly into GLP/GMP environments requiring audit-ready parameter logging and hardware-level traceability.

Key Features

  • 20-position autosampler carousel with automatic vial detection and intelligent position skipping—avoids mechanical collision during operation even if vials are missing or misloaded.
  • Triple-zone independent temperature control: sample oven (40–220 °C), valve block (40–220 °C), and transfer line (40–220 °C), all configurable up to 300 °C upon request; stability maintained at < ±0.5 °C for analytical repeatability.
  • Heated 6-port valve with integrated 1 mL quantitative loop (optionally 0.5/2/5 mL); valve and loop housed entirely within the thermal zone to eliminate cold spots and ensure analyte integrity during transfer.
  • Positive-pressure sampling mechanism—enables direct analysis of liquids and solids without derivatization or extraction; eliminates baseline drift associated with split/splitless GC inlet overloading.
  • Fully deactivated flow path using imported high-inertness tubing and silanized components—minimizes adsorption, carryover, and cross-contamination; validated RSD < 1.0% (n = 6) for 100 ppm ethanol in aqueous matrix.
  • Motor-driven actuation—no external compressed air or nitrogen required; reduces facility dependency and improves operational safety in confined lab spaces.
  • 7-inch full-color TFT LCD interface with animated workflow guidance; supports standalone operation or full remote control via USB-connected PC running vendor-neutral software.
  • Configurable timing resolution down to 1 ms; programmable pressurization, equilibration, sampling, injection, and purge cycles—supports ASTM D7217, EPA Method 502.2, and ISO 11843-2 compliant protocols.

Sample Compatibility & Compliance

The LAHS-20A Plus accommodates standard 10 mL and 20 mL crimp-top headspace vials (also compatible with 50 mL and 100 mL custom formats). It handles heterogeneous matrices including aqueous solutions, soil slurries, polymers, pharmaceutical tablets, beverages, and biological tissues. All wetted surfaces meet USP Class VI biocompatibility requirements. The instrument supports 21 CFR Part 11-compliant data integrity when paired with validated chromatography data systems (CDS), offering electronic signatures, audit trails, and user-access-level permissions. Firmware includes self-diagnostics: automatic carousel homing, real-time heater fault detection, pressure sensor validation, and communication handshake verification—critical for regulated QC/QA labs undergoing FDA or NMPA inspections.

Software & Data Management

Control and method development are performed via a dedicated Windows-based application supporting multi-method scheduling, sequence queueing, and real-time status monitoring. All parameters—including temperature ramps, pressure profiles, timing events, and GC trigger logic—are stored as encrypted XML files with timestamped revision history. Raw method files include metadata fields for analyst ID, instrument serial number, and calibration certificate references. Export options include CSV and PDF reports compliant with ISO/IEC 17025 documentation standards. Optional EPC (Electronic Pressure Control) module enables closed-loop carrier gas regulation synchronized with headspace pressurization—enhancing retention time stability across long unattended runs.

Applications

  • Residual solvent quantification in active pharmaceutical ingredients (APIs) per ICH Q3C guidelines.
  • VOC screening in drinking water per EPA Method 524.4 and ISO 15681-2.
  • Flavor compound profiling in dairy, wine, and fermented products.
  • Automotive interior material emissions testing (VDA 278, ISO 12219-4).
  • Forensic blood alcohol and volatile toxin analysis (e.g., acetone, isopropanol, methanol).
  • Quality control of packaging materials for leachable organics (e.g., ethylene oxide, formaldehyde).

FAQ

Does the LAHS-20A Plus support regulatory-compliant audit trails?
Yes—when operated with validated CDS software, it logs all parameter changes, run start/stop events, and system errors with immutable timestamps and user attribution.
Can it be integrated with third-party GC systems?
Yes—it provides TTL-level GC start triggers, analog/digital I/O ports, and USB HID emulation for plug-and-play compatibility with Agilent, Thermo Fisher, Shimadzu, PerkinElmer, and国产 GC platforms.
Is method transfer between LAHS-20A Plus units straightforward?
Absolutely—method files are portable across instruments of the same firmware version; calibration constants (e.g., pressure sensor offsets) are stored separately to preserve inter-unit comparability.
What maintenance intervals are recommended for routine operation?
Valve maintenance every 6 months or 2,000 injections; quantitative loop cleaning after every 500 injections; annual verification of temperature accuracy per ISO 17025 clause 6.4.10.
How does the system handle vial sealing integrity verification?
It monitors real-time pressure rise during pressurization; deviations beyond ±5% of setpoint trigger automatic abort and error logging—preventing false-negative results from leaky crimps.

InstrumentHive
Logo
Compare items
  • Total (0)
Compare
0