← Water Treatment Applications

Pharmaceutical & Purified Water Treatment

Purified-water systems require control of both water quality and the distribution environment. Ozone may be considered for a validated sanitisation strategy where the equipment and points of use support that approach.

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The Treatment Challenge

Microbial growth can develop in storage, circulation loops and poorly managed stagnant areas. Sanitisation must be coordinated with water production and use, because an acceptable treatment stage does not automatically establish acceptable water at every outlet.

How Ozone Helps

Ozone can contribute to microbial control in compatible storage and distribution arrangements. It does not remove dissolved salts or replace purification, and microbiological suitability must be established through the system’s validation and monitoring programme.

Process engineering

Technical Treatment Approach

A prepared oxygen feed and generator supply a controlled injection point in the water loop. Flow, mixing and ozone residual are reviewed at relevant locations. Vent off-gas requires treatment, and residual removal must be verified before uses that cannot tolerate ozone.

Key Benefits

  • Supports a defined loop-sanitisation strategy
  • Can be monitored at selected storage and return points
  • Allows coordination between sanitisation and production modes

System Integration

RO, deionisation and other purification equipment address their respective contaminants. UV may be used for validated ozone destruction, while hygienic piping, drainage and circulation design remain essential to the overall water system.

Engineering & Automation

PLC and HMI options can separate production, sanitisation and release-to-use sequences. Residual sensors, alarm records, interlocks and remote supervision may support traceability without replacing authorised water-release decisions.

Available depending on system configuration and project requirements.

Important Design Considerations

Water chemistry, recirculation flow, microbial load and intended use govern dose, contact time, transfer efficiency and demonstrated performance. Confirm materials compatibility, residual removal and validation requirements; no pharmaceutical approval is implied by ozone use alone.

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