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UIC KD10 Short-Path Molecular Distillation System

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Brand UIC GmbH
Origin Germany
Model KD10
Feed Rate 8–15 kg/h
Effective Evaporation Area 10 dm²
Evaporator Internal Diameter 20 cm
Condenser Area 15 dm²
Collecting Flasks 2
Construction Material ASTM A240 UNS S31603 (1.4571) Stainless Steel
Max Evaporation Temperature 350 °C
Min Operating Pressure 1 mbar
Heating Method Thermostatic Oil Bath
Independent Zone Heating Evaporator Surface, Feed Line, Distillate Outlet

Overview

The UIC KD10 Short-Path Molecular Distillation System is a precision-engineered laboratory-scale purification platform designed for thermal-sensitive, high-boiling-point, and viscous compounds under ultra-high vacuum conditions. Based on the physical principle of molecular distillation—where separation occurs when the mean free path of vapor molecules exceeds the distance between evaporator and condenser surfaces—the KD10 enables efficient fractionation without bulk boiling or prolonged thermal exposure. Its short-path geometry (typically <50 mm gap), combined with a dynamic self-cleaning roller film mechanism, ensures minimal residence time (<30 seconds), high surface renewal rates, and exceptional thermal stability control. The system is purpose-built for applications requiring high-purity isolates from natural extracts, pharmaceutical intermediates, polymer additives, and specialty chemicals—particularly where conventional vacuum distillation induces decomposition or oxidative degradation.

Key Features

  • Self-cleaning roller film evaporator with precise speed control (0.1–120 rpm), ensuring uniform thin-film formation and preventing fouling or localized overheating
  • Independent thermostatic heating zones for evaporator wall, feed preheater, and distillate outlet—each regulated to ±0.5 °C via integrated Pt100 sensors and PID controllers
  • High-integrity vacuum architecture rated for continuous operation down to 0.5 mbar (absolute), compatible with dual-stage rotary vane pumps and optional cold traps
  • Evaporator constructed from ASTM A240 UNS S31603 (1.4571) stainless steel—electropolished to Ra ≤ 0.4 µm and passivated per ASTM A967—ensuring corrosion resistance and compliance with FDA-relevant surface finish standards
  • Modular design supporting optional upgrades: integrated digital pressure transducer with real-time logging, motorized fraction collector with programmable timed switching, and inert gas purging interface (N₂ or Ar)
  • CE-marked mechanical assembly with integrated safety interlocks, overtemperature cutoffs, and vacuum loss shutdown protocols aligned with EN 61000-6-2/6-4 EMC directives

Sample Compatibility & Compliance

The KD10 accommodates feedstocks ranging from low-viscosity oils (e.g., fish oil ethyl esters, ~50 cSt at 40 °C) to highly viscous materials (e.g., squalene, tocopherol concentrates, or polymer oligomers up to 5,000 cSt). Feed introduction is gravity-fed or pump-assisted via calibrated peristaltic or diaphragm metering systems (not included), with inlet temperature independently controlled to prevent premature crystallization or polymerization. All wetted surfaces comply with USP Class VI biocompatibility requirements. The system supports documentation workflows aligned with GLP (OECD 174) and GMP Annex 15 traceability standards; audit trails for temperature, pressure, and runtime are exportable in CSV format for regulatory submission.

Software & Data Management

The KD10 operates via a dedicated UIC Control Panel (UCP) interface—a touchscreen HMI running embedded Linux with deterministic real-time I/O handling. Process parameters (evaporator temp, condenser temp, feed rate setpoint, vacuum level) are logged at 1 Hz resolution with timestamped metadata. Data files conform to ISO/IEC 17025-compliant naming conventions and include checksum validation. Optional UIC DataLink software (Windows-based) enables remote monitoring, multi-unit fleet synchronization, and automated report generation compliant with FDA 21 CFR Part 11—featuring electronic signatures, role-based access control, and immutable audit logs with user action timestamps.

Applications

  • Purification of thermolabile nutraceuticals: removal of PCBs, dioxins, and heavy metals from omega-3 concentrates while preserving EPA/DHA integrity
  • Isolation of active pharmaceutical ingredients (APIs): separation of cannabinoid fractions (CBD, CBG, Δ9-THC) from crude hemp extract with >98% recovery yield
  • Refinement of synthetic lubricant base stocks: deodorization and monomer removal from polyalphaolefins (PAOs) under <1 mbar
  • Recovery of high-value fragrance compounds: selective isolation of ionones and damascones from rose oil distillates without thermal rearrangement
  • Recycling of spent catalysts: extraction of residual metal complexes (e.g., Rh, Pd) from reaction residues prior to incineration

FAQ

What vacuum level is required for optimal performance of the KD10?

The system is engineered for stable operation at 0.5–5 mbar absolute; for molecular distillation of high-molecular-weight lipids (e.g., triglycerides), pressures ≤1 mbar are recommended to maximize mean free path and minimize back-migration.
Can the KD10 be integrated into an existing lab vacuum infrastructure?

Yes—the unit features standardized KF-40 vacuum flanges and accepts standard DN25/NPT 1/2″ vacuum line connections; compatibility with existing pumps, gauges, and cold traps must be verified per ISO 2859-1 sampling plans.
Is validation support available for GMP environments?

UIC provides IQ/OQ documentation templates, calibration certificates traceable to DKD/DAkkS standards, and on-site protocol execution support—subject to site-specific risk assessment per ICH Q9.
What maintenance intervals are recommended for the roller film mechanism?

Roller bearings and scraper blades require inspection every 500 operational hours; full lubrication and torque verification per DIN 33200 is advised annually or after 2,000 h—whichever occurs first.

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