

Solvent Recovery Vacuum Drying Oven
溶剂回收真空干燥箱
- SKU VAO-0004
- Vacuum Ovens
- CE (to be confirmed)
- ISO 9001 manufacturing (to be confirmed)
- RoHS (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Chamber volume | 20–100 L |
|---|---|
| Temperature range | RT+10 to 200 C |
| Ultimate vacuum | ≤133 Pa |
| Trap temperature | -40 to -80 C |
| Recovery vessel | 1–5 L glass or steel |
| Gasket material | Fluororubber or PTFE |
By Lab Manufacturers China Technical TeamLast reviewed Standards: IEC 61010-1, IEC 61010-2-010, DIN 12880
What is the Solvent Recovery Vacuum Drying Oven?
A solvent recovery vacuum drying oven captures evaporated solvent in a cold trap or condenser instead of releasing it to the pump. It is selected when samples contain flammable or valuable solvents that must be recovered safely.
What is the Solvent Recovery Vacuum Drying Oven?
A solvent recovery vacuum drying oven captures evaporated solvent in a cold trap or condenser instead of releasing it to the pump. It is selected when samples contain flammable or valuable solvents that must be recovered safely.
Overview
This vacuum oven is built around solvent handling. A cold trap or condenser sits between the chamber and the pump, condensing vapour so that pump oil, seals and the environment are protected. Recovery vessels collect the condensate for reuse or disposal. The chamber, gasket and piping use solvent-resistant materials, often fluororubber or PTFE seals and stainless steel wetted parts. An inert-gas purge can be added to lower oxygen before drying, and explosion-proof configurations are available where solvent loads are high. Temperature reaches 200 C, and vacuum is typically 133 Pa or better. Vented exhaust and solvent-resistant pumps complete the system, making it suitable for chemical, pharmaceutical and battery materials work.
How does it work?
A vacuum oven removes air from a sealed chamber with a pump, lowering the boiling point of water and solvents so evaporation proceeds quickly at moderate temperature. The chamber is a thick-walled vessel, usually stainless steel, with a reinforced door, silicone or fluororubber gasket and a transparent window. Heating comes from elements in the walls, a water or oil jacket, or heated shelves, so most heat reaches the sample by conduction and radiation rather than convection. A Pt100 sensor and PID controller hold the setpoint, while a vacuum gauge or sensor displays chamber pressure. Cold traps, solvent recovery units and inert-gas purge connections can be added for solvent-laden samples. The mild cycle protects thermolabile and easily oxidized materials.
What are the key features?
- Cold trap or condenser rated for solvent condensation
- Solvent-resistant gasket, piping and stainless steel wetted parts
- Recovery vessel for condensate collection
- Optional inert-gas purge and explosion-proof configuration
- Vented exhaust and solvent-resistant pump compatibility
- Digital PID controller with vacuum gauge
What are the technical specifications?
A typical solvent recovery vacuum drying oven configuration offers chamber volume of 20–100 L, temperature range of RT+10 to 200 C, ultimate vacuum of ≤133 Pa, trap temperature of -40 to -80 C, recovery vessel of 1–5 L glass or steel and gasket material of Fluororubber or PTFE. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Solvent Recovery Vacuum Drying Oven is used in drying solvent-wet powders, battery and electronic materials processing, pharmaceutical intermediate drying, chemical sample preparation and recovery of costly solvents. Across the wider Vacuum Ovens class, laboratories also deploy it for heat-sensitive powder drying, degassing of liquids and resins and drying electronic and optical components.
Which standards and certifications apply?
Relevant standards and methods include IEC 61010-1, IEC 61010-2-010, DIN 12880, ISO 9001 and GB/T 30435. Certification candidates for this model are CE, ISO 9001 manufacturing and RoHS; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Vacuum ovens need a compatible pump, usually a rotary-vane or dry pump, and for solvent work a cold trap to protect the pump and recover vapour. Never use a vacuum oven as a pressure vessel, and never open the door until the chamber is vented to atmosphere. Place the oven on a stable surface with pump clearance and route exhaust safely. Calibrate temperature and verify vacuum tightness periodically, checking the door gasket for wear and replacing it as needed. Clean shelves and chamber after solvent use, and keep a log of pump oil changes or dry-pump service.
How do I select the right Solvent Recovery Vacuum Drying Oven?
Select a solvent recovery oven whenever the sample carries flammable or valuable solvent, or when local rules restrict vapour release. Standard vacuum ovens are unsuitable for these loads. In the RFQ, specify solvent type and volume, trap temperature, recovery vessel size, purge gas and whether an explosion-proof build is needed.
How does it compare with other Vacuum Ovens variants?
Choose a vacuum oven when the sample degrades at the drying temperature, oxidizes in air, or contains a solvent that must be recovered. Start with chamber volume and shelf area against batch size, then set temperature range, usually up to 200 or 250 C, and the required ultimate vacuum, from about 133 Pa for general drying to below 10 Pa for demanding work. Decide whether you need heated shelves for better conduction or a jacket-heated chamber. Check the gasket and window material if aggressive solvents are used, and specify a cold trap or solvent recovery unit. Confirm pump compatibility, controller profile, safety interlocks and electrical supply.
Full specifications
| Chamber volume | 20–100 L |
|---|---|
| Temperature range | RT+10 to 200 C |
| Ultimate vacuum | ≤133 Pa |
| Trap temperature | -40 to -80 C |
| Recovery vessel | 1–5 L glass or steel |
| Gasket material | Fluororubber or PTFE |
| Purge gas | Nitrogen or argon |
| Temperature uniformity | ±2–4 C |
| Heating power | 1–2.5 kW |
| Power supply | 220 V, 50/60 Hz |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Drying solvent-wet powders
- Battery and electronic materials processing
- Pharmaceutical intermediate drying
- Chemical sample preparation
- Recovery of costly solvents
Key features
- Cold trap or condenser rated for solvent condensation
- Solvent-resistant gasket, piping and stainless steel wetted parts
- Recovery vessel for condensate collection
- Optional inert-gas purge and explosion-proof configuration
- Vented exhaust and solvent-resistant pump compatibility
- Digital PID controller with vacuum gauge
Frequently asked questions about Solvent Recovery Vacuum Drying Oven
Evaporated solvent passes through a cold trap or condenser held well below its dew point, where it liquefies and drains into a recovery vessel. This protects the vacuum pump and allows the solvent to be reused or disposed of properly.
Not automatically. Explosion protection depends on the build, including motor and electrical ratings and purge design. Where flammable vapour concentrations can occur, an explosion-proof configuration with inert-gas purge and safe venting is required and must be verified for the site.
A trap at -40 to -80 C condenses most common solvents such as ethanol, acetone, methanol and hexane. Very volatile solvents may need a colder trap or a two-stage condenser. Trap temperature must stay well below the solvent dew point at the working vacuum.
Under vacuum, water and solvents boil at lower temperature, so samples dry faster and at lower heat, with less oxidation. This protects thermolabile, oxygen-sensitive and reactive materials that would degrade in a conventional oven.
Typical chambers reach about 133 Pa with a rotary-vane pump, and below 10 Pa with a two-stage pump and good seals. Practical working pressure also depends on the vapour load, so drying usually occurs at a few hundred to a few thousand pascals.
A cold trap is recommended whenever solvents or large amounts of water are evaporated. It condenses vapour before it reaches the pump, protecting pump oil and seals and allowing solvent recovery. It is less critical for dry, low-vapour samples.
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