Raypa VACUTERM Series Vacuum Drying Oven
| Brand | Raypa |
|---|---|
| Origin | Spain |
| Model | VACUTERM |
| Instrument Type | Vacuum Oven |
| Temperature Range | 35–200 °C |
| Temperature Uniformity | ±4 °C |
| Temperature Stability | ±1 °C |
| Temperature Display Accuracy | ±2 °C |
| Maximum Vacuum Level | 0.01 mbar |
| Chamber Dimensions (W×D×H) | 34 × 32 × 32 cm |
| External Dimensions (W×D×H) | 62 × 53 × 49 cm |
| Chamber Material | AISI 304 Stainless Steel |
| Door & Interior Trim | AISI 304 Stainless Steel |
| Shelving | 2 Perforated Aluminum Shelves (Epoxy-Coated) |
| Heating Method | Forced-Air Circulation |
| Safety Compliance | EN 61010-1, EN 61010-2-010 |
| Temperature Sensor | PT100 Platinum Resistance Thermometer |
| Controller | Digital Microprocessor-Based Time-Temperature Controller |
| Safety Features | Dual-Level Independent Temperature Limiter, Tempered Double-Glazed Safety Glass Door, Silicone Sealing Gasket |
Overview
The Raypa VACUTERM Series Vacuum Drying Oven is a precision-engineered laboratory instrument designed for controlled thermal processing under reduced pressure environments. Operating on the principle of vacuum-assisted moisture removal—where lowering ambient pressure reduces the boiling point of solvents and volatile compounds—the VACUTERM enables gentle, uniform drying of thermally sensitive, hygroscopic, or oxidation-prone samples without structural degradation. Unlike conventional forced-air ovens, vacuum drying minimizes oxidative damage, prevents surface hardening, and eliminates solvent residue carryover—critical for pharmaceutical active ingredient isolation, polymer characterization, catalyst regeneration, and analytical sample preparation. Engineered for reproducibility and regulatory traceability, the VACUTERM meets foundational safety and electromagnetic compatibility requirements per EN 61010-1 and EN 61010-2-010, making it suitable for GLP-compliant laboratories and ISO 17025-accredited testing facilities.
Key Features
- Forced-air circulation heating system ensures rapid thermal equilibration and consistent temperature distribution across the chamber volume
- Dual-stage independent temperature protection: primary PID-controlled microprocessor regulator plus secondary mechanical safety limiter (Class 2), preventing uncontrolled thermal excursion
- Tempered double-glazed safety glass door with silicone gasket seal provides visual monitoring while maintaining vacuum integrity and mitigating implosion risk
- AISI 304 stainless steel chamber, interior door panel, and shelf supports resist corrosion from acidic vapors, solvents, and repeated sterilization cycles
- PT100 platinum resistance thermometer delivers high-stability temperature feedback with long-term drift <0.1 °C/year under calibrated conditions
- Digital microprocessor-based time-temperature controller supports programmable ramp-hold profiles and real-time deviation logging
- Epoxy-coated external housing enhances durability in shared lab environments and resists chemical splashes and abrasion
- Integrated vacuum port compatible with standard rotary vane or diaphragm vacuum pumps (not included); achieves stable operation at ≤0.01 mbar
Sample Compatibility & Compliance
The VACUTERM accommodates a broad spectrum of sample types—including lyophilized biologicals, ceramic precursors, battery electrode slurries, chromatographic stationary phases, and residual solvent analysis standards—without cross-contamination or catalytic interference. Its inert stainless-steel construction complies with USP material compatibility guidelines for pharmaceutical contact surfaces. The vacuum chamber design conforms to ASTM E145-22 (Standard Specification for Gravity-Convection and Forced-Ventilation Ovens) and supports method validation per ICH Q5C (Quality of Biotechnological Products: Stability Testing). All electrical and thermal safety systems are certified to EN 61010-1 (General Safety Requirements for Electrical Equipment for Measurement, Control, and Laboratory Use) and EN 61010-2-010 (Particular Requirements for Laboratory Ovens), ensuring suitability for CE-marked installations in EU-regulated laboratories.
Software & Data Management
An optional PC interface module enables RS-232 or USB connectivity for remote parameter configuration, real-time data streaming, and automated report generation. When paired with Raypa’s proprietary control software (sold separately), users gain access to audit-trail-enabled operation logs compliant with FDA 21 CFR Part 11 requirements—including user authentication, electronic signatures, and immutable timestamped event records (e.g., setpoint changes, vacuum level deviations, door open/close events). Data export supports CSV and XML formats for integration into LIMS or ELN platforms. Firmware updates are delivered via secure signed packages, preserving system integrity during lifecycle maintenance.
Applications
- Pharmaceutical: Residual solvent removal from APIs and excipients prior to tablet compression; moisture content determination per USP
- Materials Science: Degassing of composite preforms, binder burnout in powder metallurgy, and thermal aging studies of polymeric films
- Food & Agriculture: Low-temperature dehydration of enzyme-rich botanical extracts and pesticide residue reference standards
- Environmental Testing: Preparation of soil and sediment samples for gravimetric water content analysis (ISO 11465)
- Academic Research: Solvent exchange protocols in MOF synthesis, vacuum annealing of thin-film photovoltaic layers, and stability screening of nanocarrier formulations
FAQ
What vacuum pump is recommended for optimal performance with the VACUTERM?
A two-stage rotary vane pump with ultimate vacuum ≤0.005 mbar and oil mist filter is recommended for continuous operation at 0.01 mbar. Diaphragm pumps may be used for intermittent low-load applications.
Can the VACUTERM be validated for GMP environments?
Yes—its microprocessor controller supports IQ/OQ documentation templates, and all critical parameters (temperature, vacuum, time) are digitally recorded with configurable sampling intervals. Full 3Q validation support documentation is available upon request.
Is over-temperature protection hardware-based or software-dependent?
It is fully hardware-redundant: a Class 2 mechanical safety thermostat operates independently of the main controller and cuts power to the heating elements if the chamber exceeds the user-defined safety threshold.
Are replacement shelves and gaskets available as spare parts?
Yes—AISI 304 stainless steel shelves, perforated aluminum shelves, and high-temperature silicone door gaskets are stocked and shipped globally with traceable part numbers.
Does the unit include a vacuum gauge?
Yes—a calibrated analog Bourdon-tube vacuum gauge (0–1000 mbar range) is integrated into the front panel for immediate visual verification of chamber pressure status.


