A truly sanitary CIP-capable heat exchanger must be engineered from the start with polished surfaces, full drainability, no dead legs, and cleanable connections — allowing automated cleaning cycles to achieve complete soil and microbial removal.
Sanitary CIP heat exchangers are specifically constructed to withstand aggressive cleaning chemicals and high-velocity flow while achieving log reductions in bacteria — ensuring food safety and regulatory compliance in hygienic processes.
True sanitary CIP goes beyond basic cleaning — it requires equipment designed to be cleaned in place effectively every time. This means polished surfaces, drainable geometry, and turbulence-capable flow paths that remove soil and kill microbes consistently.
Properly designed units support validated cleaning protocols required by FDA, USDA, and PMO standards.
All product-contact surfaces must be 316L stainless steel with Ra less than or equal to 32 microinch mechanical polish (20 microinch electropolished preferred). No pits, cracks, or discoloration allowed.
Heat exchangers must drain completely when shut down. No horizontal tubes, no trapped areas. All ports and branches follow less than or equal to 2D rule to prevent stagnant zones.
Designed for greater than 5 ft/s (1.5 m/s) velocity during CIP to achieve Reynolds numbers greater than 4,000 — creating mechanical scrubbing action essential for soil removal.
Only sanitary clamp or permanent weld connections. Elastomers must be FDA/3-A compliant and fully encapsulated or flush-mounted to prevent entrapment.
Riboflavin coverage testing proves 100% wetting. Microbial challenge tests and ATP swabbing confirm sanitary condition post-CIP. Documentation included with every unit.
In food and pharma, ineffective cleaning leads to recalls, spoilage, or contamination. Sanitary CIP-capable heat exchangers eliminate risk and ensure consistent product safety.
It means the heat exchanger is specifically designed and constructed to be fully cleaned and sanitized in place using automated CIP — achieving hygienic condition without disassembly.
No — only units built with polished sanitary surfaces, drainable design, and no dead zones can be reliably cleaned in place.
Minimum Ra less than or equal to 32 microinch (0.8 micrometer) mechanical polish; 15-20 microinch electropolished preferred for pharma and high-risk foods.
Residual product or cleaning solution left in pockets becomes a microbial growth site and prevents proper sanitization.
Yes — due to higher-grade materials, precision fabrication, and certification — but they save significantly on labor, downtime, and risk.
Through riboflavin coverage testing (100% wetting), ATP swabbing, and microbial plate counts after validated CIP cycles.