280L Horizontal Cylindrical Autoclave HCPS-D280

280L Horizontal Cylindrical Autoclave HCPS-D280

Features:

• Implements gravity exchange principle to create pure steam environment by eliminating residual cold air.
• Automated temperature-based steam control ensures precise sterilization conditions throughout each cycle.
• Suitable for diverse applications including medical device sterilization and laboratory media processing.
• Simplified automated operation with programmable drying function for post-sterilization preparation.
• Comprehensive safety package: automatic over-limit protection, water deficiency detection with alarm shutdown.
• Mechanical pressure interlock prevents door access above 0.027MPa and requires proper sealing for startup.
• Pressure relief valve automatically opens at 0.24MPa, directing excess steam to integrated water tank.
• All-stainless steel construction with integrated documentation printer for quality assurance compliance.

Specifications

Introduction about autoclave

The term "autoclave" is synonymous with reliable sterilization in professional settings. This device operates on the principle that moist heat under pressure is microbicidal. By creating an environment of saturated steam at temperatures like 121°C or 134°C, it achieves what dry heat cannot at equivalent temperatures: rapid and deep penetration. The sterilization cycle is methodical.

First, the removal of air is critical; any residual air creates cold spots and prevents steam contact. Second, the exposure phase delivers the lethal conditions. Third, exhaust returns the chamber to ambient pressure, often aided by a vacuum to dry contents. This process is vital for sterilizing heat-resistant surgical tools, dental equipment, and a wide range of laboratory supplies. Laboratories depend on it to prepare culture media and decontaminate waste. Its use even spans into industrial sectors for materials processing. The rationale for its universal adoption is clear: it offers a non-toxic, rapid, and highly effective means of achieving sterility assurance, capable of inactivating the most persistent biological agents, which is why it remains the benchmark against which other methods are measured.