This page explains how Vacuum Processing Chamber is classified within Computer, Electronic and Optical Product Manufacturing. Technical values and manufacturer relationships are research references; confirm the current specification and supplier evidence for each order.
A sealed enclosure designed to maintain a controlled vacuum environment for processing components within a medical imaging system production line.
Technical details and manufacturing context for Vacuum Processing Chamber
| Parameter | Typical range | Notes & selection driver |
|---|---|---|
| Chamber Volume | 50–200 L | Determines batch size for processing components. |
| Ultimate Pressure | 1e-3–1e-2 Pa | Lower pressure enables cleaner vacuum environment. |
| Leak Rate | ≤1e-9 Pa·m³/s | Critical for maintaining vacuum integrity.ISO 21360 |
| Operating Temperature | 15–40 °C | Affects material stability and process consistency. |
| Heating Rate | 5–10 °C/min | Controls thermal uniformity during processing. |
| Temperature Uniformity | ±5 °C | Ensures consistent processing across chamber. |
| Electrical Supply | 380–480 V AC | Three-phase power for heaters and pumps.IEC 60038 |
| Power Consumption | 5–15 kW | Affects operating cost and facility capacity. |
| Ingress Protection | IP54–IP65 | Protects against dust and water ingress.IEC 60529 |
| Chamber Material | 316L | Corrosion-resistant stainless steel for cleanroom use.ASTM A240 |
| Weight | 500–1500 kg | Consider floor loading and handling requirements. |
| Footprint | 1.5–3.0 m² | Space needed for installation and maintenance. |
Ranges are indicative industry figures for RFQ preparation, not a supplier commitment. Confirm every value and standard with the legal manufacturer before ordering.
| pressure: | 10^-6 Torr to 760 Torr (vacuum to atmospheric pressure) |
| flow rate: | 0-100 sccm (standard cubic centimeters per minute) for process gas introduction |
| temperature: | +15°C to +40°C |
| slurry concentration: | Not applicable - dry processing environment required |
Indicative industry ranges for design and RFQ preparation. Confirm the exact figures and applicable standard with the manufacturer before specifying.
Quoted from the published standard.
Manufacturer profiles associated with Vacuum Processing Chamber.
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A practical evidence checklist for RFQ preparation and supplier evaluation.
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It provides a controlled low-pressure environment for processes like thin-film deposition, degassing, or assembly of medical imaging components, ensuring contamination-free conditions.
Chamber volume (50-200 L), ultimate pressure (1e-3 to 1e-2 Pa), leak rate (≤1e-9 Pa·m³/s per ISO 21360), operating temperature (15-40 °C), and electrical supply (380-480 V AC). Always confirm with the manufacturer.
Through use of stainless steel 316L, high-vacuum compatible ceramics, and borosilicate glass viewports, plus a low leak rate as per ISO 21360. Regular leak testing is recommended.
The chamber weighs 500-1500 kg and has a footprint of 1.5-3.0 m². It requires a three-phase power supply and adequate floor loading capacity. Verify with the supplier.
Editorial classification, named public sources where available, and source-reviewed manufacturer records.
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