
Weldcoa’s Medical CO₂ Purification System is designed to support customers who want to purify beverage/industrial-grade CO₂ into USP-grade CO₂ using a controlled phase-change (distillation/condensation) process.
Instead of relying solely on inline filtration, this system uses a batch purification approach that allows customers to strengthen supply continuity, reduce dependence on external suppliers, maintain control over USP CO₂ production and validate product quality using their own procedures. This is a modular, engineered solution built to integrate into real-world operations — not a one-size-fits-all package.
USP CO₂ is medical-grade carbon dioxide commonly used in healthcare and laboratory applications. While final product qualification is the customer’s responsibility, typical industry characteristics include:
Typical Characteristics
Common Medical Uses
Final product compliance is determined by the customer’s own testing and procedures.
This batch-based process provides structure, traceability, and control.

Many systems attempt to improve CO₂ quality using inline filtration alone. Weldcoa’s system leverages phase-change purification, where separation occurs during condensation.
The Theory of Operation is as follows:
The purification system operates based on controlled phase transition and selective impurity removal. The heavy impurities remain in the liquid phase of the Beverage Grade tank and only the CO2 vapor is transferred to the USP tank. When CO2 vapor is cooled and condensed back into a liquid, impurities that do not condense at the same temperature are separated and left behind. This method is significantly more effective than inline filtration because it eliminates contaminants at the liquid phase, ensuring only high-purity CO2 is retained. The process leverages automated controls and monitoring to optimize efficiency and maintain compliance with USP standards.
This proven approach supports true purification — not just filtration.
Superior Impurity Removal: Unlike inline purification systems that rely on carbon filtration (which may not remove all harmful impurities), this method effectively traps contaminants in the liquid phase, preventing them from reaching the medical-grade supply.
Scalability: The system can accommodate different bulk tank sizes, allowing flexibility based on production demands.
Automated Operation: The HMI touchscreen interface simplifies control and monitoring, reducing manual intervention.
Regulatory Compliance: System operation supports FDA and USP validation requirements, streamlining compliance processes for customers.
Compliance and Validation Support: Customers can leverage third-party expertise (such as Asterisk) to assist with FDA documentation, validation, and qualification procedures.
Ideal for:
Not ideal for:
Because every site is different, Weldcoa offers a modular solution tailored to the facility.
Common scenarios include:
Each system is engineered around the customer’s equipment and goals.
Depending on configuration, Weldcoa typically provides:
Commissioning focuses on:
Successful USP CO₂ programs require customer participation. Customers are responsible for:
This keeps ownership of compliance with the customer while Weldcoa focuses on equipment integrity.
Because every facility is different, the next step is a conversation.
Our team will review:
Contact Weldcoa at solutions@weldcoa.com today to begin the evaluation.
HAve a special application?For any questions on what is offered or if you have a specialty application, please feel free to contact us at (630) 806-2000 or email us at solution@weldcoa.com.


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Located in Aurora, IL, Weldcoa is an innovative US manufacturer of products that store, transport, fill, supply and/or analyze compressed gas, cryogenic liquids, high pressure liquids and supercritical fluid. Our cross-disciplinary team of experts bring an in-depth knowledge of gases to every project. You can count on their passion and commitment to make your project a success.
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