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Frontier Lab Medium Pressure Flow controller - Optional accessory for Tandem and Single μ-Reactors

Brochures and specifications |  | Frontier LabInstrumentation
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Summary

Importance of the Topic


Accurate real‐time analysis of catalytic reactions under elevated pressures is essential for process optimization in research and industry. Conventional gas chromatography often exhibits shifting retention times when operating above atmospheric pressure, leading to reproducibility issues and complicating kinetic studies. The MP-3050FC medium pressure flow controller offers a solution by maintaining stable retention times up to 0.98 MPa, enabling direct online monitoring of reaction products without modifying existing chromatographic hardware.

Objectives and Study Overview


  • Demonstrate online GC analysis of catalytic reaction products under medium pressure (up to 1 MPa).
  • Verify that retention times remain constant across a range of pressures.
  • Illustrate compatibility with existing GC systems, columns, and detectors.
  • Showcase simple upgrade paths for Tandem and Single µ-Reactor setups.

Methodology and Instrumentation


  • Reaction system: Tandem/Singe µ-Reactors with H-ZSM-5 catalyst at 250 °C converting ethanol to ethylene.
  • Carrier gas: Helium at 100 mL/min; sample injection: 1 µL ethanol; split ratio: 1/100.
  • GC parameters: UA1-30M-2.0F column; oven program: 30 °C (4 min) to 230 °C at 20 °C/min; detector: FID.
  • Medium Pressure Flow Controller MP-3050FC features:
    • Pressure control range 0.3–0.98 MPa using the GC head pressure controller.
    • Digital display of column head pressure.
    • Compatible gases: He, H₂, N₂, etc.
    • Standard accessories: deactivated restrictor tube (0.15 φ × 4 m) and Open Split interface.
    • Power requirements: 100/240 VAC, 50 W.

Main Results and Discussion


  • Retention times of ethylene remained constant across pressures from 0.07 to 1 MPa, confirming pressure-independent separation.
  • Use of a deactivated restrictor tube and Open Split interface decouples pressure effects from the analytical column.
  • No hardware modifications needed for the existing GC, separation column, or detector, preserving established analytical protocols.

Benefits and Practical Applications of the Method


  • Enables direct online monitoring of catalytic processes under realistic pressure conditions.
  • Enhances reproducibility by eliminating retention time shifts due to pressure fluctuations.
  • Facilitates rapid screening of catalysts and reaction parameters without extensive instrument reconfiguration.
  • Compatible with both Tandem and Single µ-Reactor platforms, supporting flexible reaction studies.

Future Trends and Potential Applications


  • Integration with automated reaction screening platforms and high-throughput experimentation.
  • Extension to GC/MS workflows for comprehensive product identification under pressure.
  • Application to a broader range of catalytic systems, including gas-phase and liquid-phase conversions.
  • Development of higher-pressure controllers for kinetic studies at pressures above 1 MPa.

Conclusion


The MP-3050FC medium pressure flow controller provides a robust and user‐friendly solution for maintaining consistent GC retention times in catalytic reaction studies up to 0.98 MPa. Its plug‐and‐play compatibility with existing chromatographic setups and its ability to deliver real‐time analytical data significantly improve experimental efficiency and data reliability.

References


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