Laboratory Vacuum Freeze-Drying Equipment

Laboratory Vacuum Freeze-Drying Equipment

Laboratory vacuum freeze-drying equipment executes sublimation under controlled vacuum and low-temperature conditions. This process removes solvents or water from heat-sensitive biological, pharmaceutical, and chemical samples while preserving molecular structure and biological activity.
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Description
Technical Parameters

Laboratory vacuum freeze-drying equipment executes sublimation under controlled vacuum and low-temperature conditions. This process removes solvents or water from heat-sensitive biological, pharmaceutical, and chemical samples while preserving molecular structure and biological activity.


Standard configurations integrate a hermetic refrigeration circuit, a 316L stainless steel drying chamber, a precision vacuum module, and a PLC automation terminal. Operational parameters-including shelf thermal gradients, condenser cooling curves, and chamber vacuum thresholds-are programmable to match specific eutectic point requirements. Manufactured systems comply with ISO 9001 quality standards and hold CE safety certification.

 

Product Range

 

 

Model Series

Configuration Type

Condenser Temperature

Condenser Capacity

Shelf Area

Primary Application

FD-10B

Benchtop (Top Press)

-50 deg C

3 kg / 24h

0.12 m2

Routine biological sample prep, peptides

FD-50T

Floor Standing (Manifold/Stoppering)

-80 deg C

5 kg / 24h

0.20 m2

Pharmaceutical R&D, heat-sensitive enzymes

FD-100P

Pilot Scale (External Condenser)

-80 deg C

10 kg / 24h

0.50 m2

Clinical trial batch production, scale-up

 

Technical Specifications

 

 

Specification

Details

Condenser Lowest Temperature

-50 deg C, -80 deg C (Cascade system; R404A/R23 CFC-free refrigerants).

Ultimate Vacuum Pressure

Less than 5 Pa (Unloaded, Pirani gauge; holding leak rate less than 10 Pa*L/s).

Shelf Temperature Range

-55 deg C to +70 deg C (Control precision: +/- 1 deg C; thermal uniformity less than or equal to +/- 1.5 deg C).

Defrost Mechanism

Integrated electric heating coil for rapid defrosting.

Chamber Material

316L pharmaceutical-grade stainless steel (Mirror finish: Ra less than or equal to 0.4 um).

Control Architecture

Siemens S7-1200 PLC with 7-inch industrial touch panel; supports 36 programs (40 thermal segments per program).

Data Compliance

USB/Ethernet data export conforming to 21 CFR Part 11 audit trail requirements.

Power Configuration

220V/50Hz or 110V/60Hz options available.

 

Applications

 

 

Pharmaceutical Formulation: Lyophilization of vaccines, antibiotics, monoclonal antibodies, and diagnostic reagents.


Biological Sample Processing: Preservation of live bacteria, viruses, blood plasma, and tissue samples.


Material Science: Preparation of aerogels, nanoparticles, and porous ceramic precursors.


Botanical Research: Stabilization of temperature-sensitive antioxidants and plant extracts.

 

Selection Guide

 

 

★Calculate Moisture Load: Determine maximum liquid volume per batch (kg). Condenser capacity must exceed water load by greater than or equal to 30% to prevent endpoint overloading.

 

★Determine Condenser Temperature:
50 deg C: Aqueous solutions with eutectic points above -40 deg C.
80 deg C: Formulations containing low-boiling organic solvents, carbohydrates, or low glass transition temperatures (Tg').

 

★Select Stoppering Mechanism:
Manifold Type:
Bulk flasks, ampoules, and serum bottles without in-vial sealing.
Stoppering Type: Pneumatic hydraulic sealing of rubber stoppers inside the chamber under vacuum.

 

Customization Options

 

 

01/

Vacuum Pump Integration: Edwards/Leybold oil-sealed rotary vane pumps or oil-free scroll dry vacuum pumps.

02/

Eutectic Point Sensor: Built-in resistance probe for real-time monitoring of freezing and collapse points.

03/

Cleanroom Integration: Through-wall configuration with front-loading chambers and sterile barrier flanges.

04/

Electrical Standards: Panels built for regional electrical compliance (UL/CSA certification options).

 

Quality Control & Validation

 

 

Leak Detection: Chamber assemblies tested via helium mass spectrometry down to 1 x 10^-9 Pa*m3/s.


Thermal Mapping: 9-point shelf temperature validation using calibrated thermocouple arrays. Individual test reports ship with units.


Electrical Safety: Insulation resistance (greater than or equal to 20Mohm) and dielectric withstand voltage testing executed per IEC 61010-1.


Material Traceability: 3.1 mill test certificates for 316L stainless components archived for 10 years.

 

Packaging & International Shipping

 

 

Crate Structure: Fumigation-free plywood crate lined with moisture-barrier vacuum foil and high-density EPE foam.


Accessory Kit: Vacuum oil, silicone gaskets, calibration certificates, and matching connection flanges included.


Logistics Compliance: Optimized for standard air freight pallets and 20-foot containers. Hazardous material declarations handled for refrigeration compressors.

 

Technical Support & After-Sales Service

 

 

Documentation Package: Delivered with English user manuals, electrical schematics, PLC program logic lists, and IQ/OQ protocols.


Installation: Remote video engineering support; on-site commissioning available upon contract agreement.


Warranty: 12-month standard warranty on mechanical/electrical parts; 3-year factory warranty on compressor units.


Spare Parts: Critical components (solenoid valves, vacuum gauges, door seals) stocked locally for 48-hour dispatch.

 

Frequently Asked Questions

 

 

Q: How do I choose between a -50 deg C and -80 deg C condenser?

A: Sample eutectic points dictate the requirement. Simple salt/water solutions tolerate -50 deg C. Formulations with high sugar, polymer content, or low glass transition temperatures (Tg') require -80 deg C to maintain complete solidification.

Q: Are oil-free vacuum options available?

A: Yes. While standard units use direct-drive oil-sealed rotary pumps with mist filters, oil-free scroll vacuum pumps can be specified to eliminate hydrocarbon backstreaming risks.

Q: What validation documentation is provided?

A: Factory calibration sheets and material certificates ship standard. Comprehensive IQ/OQ/PQ protocol documentation packages are available for regulated environments.

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