Aseptic blow fill system for beverage bottling

Designed for high-speed aseptic bottling, this system ensures sterility throughout the blow molding to capping process, enhancing product safety and shelf life for sensitive beverages.

Aseptically Sterilizes, Molds, Fills, and Caps Beverages

The GEA Aseptic Blow Fill System ABF 2.0 is an innovative solution for beverage and dairy producers aiming to boost production efficiency while maintaining aseptic integrity. This advanced system integrates blow molding, sterilization, filling, and capping within a single continuous operation, suited for both high and low acid beverages, including carbonated and still varieties.

With its patented dry hydrogen peroxide-based sterilization, the ABF 2.0 ensures a 6 log reduction in microbial contamination for preforms and caps. The system operates with an air recovery process that reduces energy consumption by up to 31%, maintaining environmental responsibility.

Capable of aseptic runs up to 165 hours, it handles diverse liquid products such as fruit juices, milk-based drinks, and protein shakes, ensuring flexibility and minimizing cleaning downtime to just three hours. Its fully automated PLC-controlled operations allow seamless integration into existing production lines and remote monitoring capabilities enhance operational oversight.

Constructed from chemical-resistant materials, the equipment supports rigorous sterilization protocols and meets stringent microbiological validation standards, including FDA approvals. Tailored customizable features and engineering support are available to fit specific production needs, ensuring optimal performance across various beverage processing applications.

Benefits

  • Enables extended aseptic production runs of up to 165 hours, minimizing operational pauses.
  • Lowers energy consumption with an air recovery system, cutting costs by up to 31%.
  • Ensures product safety with 6 log reduction in microbiological contamination.
  • Reduces labor intervention through fully automated sterilization processes.
  • Minimizes chemical residue with controlled vaporized hydrogen peroxide sterilization.

General


Applications
Carbonated beverages,Beverages,Milk-based drinks,Sensitive beverages,High acid beverages,Low acid beverages,Still beverages,Dairy products
End products
Lemonade,Non-dairy creamers,Milkshakes,Fruit smoothies,Tomato juice,Protein shakes,Almond milk,Iced tea,Soy milk,Sparkling water,Energy drinks,Cold brew coffee,Fermented milk drinks,Yogurt drinks,Probiotic beverages,Carbonated soft drinks,Fruit juices,Flavored water
Steps before
Preform heating,Preform sterilization,Vaporized hydrogen peroxide (VHP) treatment
Steps after
Aseptic filling,Aseptic capping,Bottle transfer
Input ingredients
preforms,caps,sterile air,hydrogen peroxide vapor
Output ingredients
high acid beverages,low acid beverages,sterilized bottles,aseptic beverages,carbonated beverages,still beverages
Market info
GEA is known for its expertise in engineering innovative and sustainable equipment and solutions, focusing on sectors such as food, beverages, pharmaceuticals, and energy, with a reputation for quality, efficiency, and advanced technological applications in industrial processing.

Technical Specifications


Shelf life compatibility
High and Low Acid Beverages
Sterilization technology
Dry Hydrogen Peroxide
Decontamination performance
6 Log Reduction
Production capacity
Continuous Runs of 165 Hours
Cleaning cycle downtime
3 Hours
Cap sterilization
Sterilcap VHP R
High reactivity and reliability
Patented Air Blowing Block

Operating Characteristics


Automation level
Full automation
Sterilization method
Hydrogen peroxide vapor (VHP)
Changeover time
Limited downtime (3 hours)
Resource efficiency
Energy consumption reduction up to 31%
Aseptic processing duration
165 hours continuous production
Microbiological validation
6 log decontamination performance
Cleaning method
Automated CIP/SIP
Cap and preform decontamination
Single sterilization phase
Flexibility
High and low acid beverage compatibility
Preform blowing process
Sterile air

Material Compatibility


Density/particle size
0.5–2.5 g/cm³ / 50–1000 µm


FDA compliance
Yes
FDA materials
Yes

Physical Characteristics


Machine footprint
Compact
Sterile zone size
Integrated sterile environment
Control panel type
Automated Control
Preform handling
Sterile neck transfer
Discharge method
Sterile transfer between modules

Custom Options


Control panel type
Touchscreen HMI
Integration possibilities
SCADA integration
Customization levels
Modular design
Automation level
Fully automated
Aseptic features
VHP sterilization
Resource-efficient technology
Air recovery system
Adjustability
Rapid changeovers
Cap sterilization options
Sterilcap VHP R