280L Horizontal Cylindrical Autoclave HCPS-C280
280L Horizontal Cylindrical Autoclave HCPS-C280
Features:
- Gravity exchange technology ensures a complete pure steam environment by efficiently purging cold air.
- Automated control system optimizes steam flow dynamically based on chamber temperature feedback.
- Designed for the sterilization needs of healthcare facilities and research institutions.
- Offers easy, automated control and a practical drying cycle for post-sterilization processing.
- Equipped with a thermal printer for automatic documentation, aiding in compliance and quality control.
- Robust safety features include auto-protection against over-temperature/pressure and water shortage with alarm.
- Mechanical door lock ensures it cannot be opened above 0.027MPa and verifies seal integrity before operation.
- Pressure relief valve set at 0.24MPa automatically vents steam to maintain safe operating limits.
- The sterilizing chamber is manufactured from premium stainless steel for durability and hygiene.
Specifications
| Model | HCPS-C280 |
| Chamber volume | 280L |
| Chamber size | φ600*1000mm |
| Working pressure | 0.22 MPa |
| Working temperature | 134℃ |
| Adjustment of temperature | 40℃ - 134℃ |
| Sterilization time | 0-99 min |
| Drying time | 0-99 min |
| Heat average | ≤± 2℃ |
| Power | 12KW/380V 50Hz |
| Dimensions | 1520*910*1900 |
| Packing size | 1680*1080*2100 |
| G.W/N.W(Kg) | 570/462 KG |
Introduction about autoclave
The autoclave process is a meticulously engineered procedure for achieving sterility. At its core, the device is a pressure vessel that heats water to generate saturated steam. Under pressure, this steam reaches temperatures lethal to microorganisms, typically 121°C or higher. The lethal effect occurs through protein denaturation and enzyme inactivation. A complete cycle involves three distinct stages: the removal of air from the chamber, the maintenance of sterilizing conditions, and the safe release of pressure and moisture. This technology is indispensable across sectors.
In medicine, it ensures reusable devices are safe for patient contact. In dentistry, it is central to instrument reprocessing protocols. In scientific research, it provides the foundation for uncontaminated experiments by sterilizing equipment and growth media. It also plays a crucial safety role in decontaminating infectious waste. Furthermore, its principles are applied industrially in processes like rubber vulcanization. The rationale for its use is compelling: it offers a reliable, repeatable, and non-residue-leaving method that is effective against the broadest range of pathogens, outperforming many chemical and dry heat alternatives in penetration and speed for most materials.
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