Pharma extraction clarifier

Achieve superior purity in pharma extraction with efficient separation of solids and liquids, seamlessly integrating into your production line while ensuring high yield and low solvent use.

Clarifies and Separates Liquid-Solid Suspensions

GEA’s Hydrohermetic Pharmaceutical Clarifier excels in liquid-solid extraction processes, especially for the pharmaceutical and biotechnological sectors. Designed with a patented hydrohermetic feed system, it minimizes shear forces, enhancing gentle handling and reducing contamination risks. The clarifier supports fully automatic, continuous operations, making it ideal for separating active pharmaceutical ingredients (APIs), monoclonal antibodies, and essential oils. Operating on the co-current, counter-current, or cross-current principles, it optimizes phase separation efficiency. With CIP capability, it ensures thorough cleaning without process disruption. Additionally, it delivers significant savings with lower solvent requirements and reduced operating costs, while high stage efficiency minimizes investment by requiring fewer stages. Constructed to meet GMP standards, it is available in corrosion-resistant materials to maintain chemical integrity.

Benefits

  • Enhances product purity with low shear forces, minimizing contamination risks.
  • Reduces operating and solvent costs with efficient phase separation processes.
  • Maximizes yield and throughput with optimized space utilization.
  • Ensures process compliance and safety with GMP-compliant construction.
  • Simplifies maintenance and cleaning through fully integrated CIP systems.

General


Applications
Liquid formulations,Fine chemicals,Nutraceuticals,Biopharmaceuticals,Pharmaceuticals
End products
High-purity enzymes,Active pharmaceutical ingredients (apis),Monoclonal antibodies,Solvent-based drug formulations,Herbal extracts,Natural flavor extracts,Nutrient-infused liquid solutions,Liquid supplements,Biotechnological vaccines,Essential oils
Steps before
Suspension Preparation
Steps after
CIP (Cleaning-In-Place),Quality Control,Packing
Input ingredients
suspensions with low solid contents,solid-liquid mixtures,pharmaceutical suspensions
Output ingredients
clarified liquids,reduced solid content,pharmaceutical extracts
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


Solid Content
Up to 7% by vol.
Automation
Fully automatic cleaning-in-place (CIP)
Control System
Controlled partial ejections
Stage Efficiency
High stage efficiency
Contact Time
Short contact times
Throughput Capacity
Optimum throughput capacity
Shear Forces
Low shear forces

Operating Characteristics


Working mechanism
Centrifugal separation
Integrated steps
Controlled partial ejections
CIP Principles
Fully automatic CIP
Batch vs. continuous operation
Continuous
Automation level
Fully automated
Feed system
Hydrohermetic feed
Stage operation
Co-current,counter-current,cross-current principles
Solvent requirement
Low
Space requirement
Minimum
Process security
High
Yield quality
Higher yield

Material Compatibility


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

Physical Characteristics


Tank shape and size
Designed for low solid content (up to approx. 7% by vol.)
Feed method
Hydrohermetic feed system
Discharge method
Partial ejections
Compact footprint
Optimized for minimum space requirement

Custom Options


Control System
PLC / SCADA
Feed System
Hydrohermetic
Ejection System
Controlled Partial Ejection
Cleaning Method
Fully Automatic CIP