Mechanical Vapor Recompression (MVR) evaporators, with their outstanding advantages such as high efficiency, energy saving, precise temperature control, and stable operation, have become essential equipment in key processes of the pharmaceutical industry, including solution concentration, solvent recovery, and wastewater treatment. The following systematically reviews the basic applications, key technologies, and practical cases of MVR evaporators in the pharmaceutical industry.
I. Main Application Scenarios
1. Pharmaceutical Mother Liquor Concentration and Product Recovery
Used for concentrating fermentation broths or synthetic liquids of antibiotics, amino acids, organic acids, vitamins, etc., increasing the concentration of target products, reducing subsequent drying load, and improving yield.
Low-temperature evaporation protects heat-sensitive substances and reduces activity loss.
2. Solvent Recovery and Reuse
Evaporation and recovery of organic solvents such as ethanol, acetone, and methanol used in large quantities in pharmaceutical production, achieving resource recycling and reducing production costs and environmental risks.
Recovered solvents have high purity and can be directly reused in production processes.
3. Pharmaceutical High-Salinity Wastewater/Organic Wastewater Treatment
Targeting pharmaceutical wastewater with high salt content, high COD, and complex composition, achieving wastewater reduction, salt crystallization, and "zero discharge" treatment.
Effectively removes harmful substances from wastewater; distilled water can be reused or discharged in compliance with standards.
4. Intermediate and Fine Chemical Concentration and Purification
Highly concentrated and crystallized pharmaceutical intermediates or fine chemical solutions, improving product purity and market value.
II. Key Application Technologies
Low-Temperature Evaporation and Thermosensitive Protection: Pharmaceutical materials are often thermosensitive. MVR (Mechanical Vapor Retention) enables low-temperature evaporation (adjusted according to the material's boiling point), effectively preventing the decomposition or inactivation of active ingredients.
Falling film evaporators and rising film evaporators are commonly used for thermosensitive materials, ensuring gentle and efficient evaporation.
Materials and Hygienic Design: Most contact parts of the equipment are made of sanitary-grade stainless steel (e.g., 316L), meeting GMP standards and preventing contamination and cross-contamination.
High surface finish and few dead corners facilitate CIP/SIP cleaning and sterilization.
Automation and Precise Control: Equipped with a PLC/DCS system, it automatically adjusts key parameters such as temperature, pressure, liquid level, and flow rate, ensuring process stability and batch consistency.
Online Monitoring and Remote Maintenance: Improves production management efficiency.
Cleaning and Cross-Contamination Prevention Strategies: Online cleaning (CIP) systems, including regular acid washing, alkaline washing, and passivation, effectively prevent residues and cross-contamination.
For multi-product production, measures such as clear/turbid water separation and segmented isolation are designed.
Energy Saving and Environmental Benefits: Primarily electricity consumption, requiring no large amounts of fresh steam; energy consumption is only 1/3 to 1/2 of traditional evaporation methods.
Highly efficient solvent recovery reduces hazardous waste disposal costs; wastewater evaporation achieves zero discharge, reducing environmental pressure.
III. Typical Application Process Analysis
Fermentation Broth Concentration Process: Fermentation broth → Pretreatment (filtration/impurity removal) → MVR low-temperature evaporation and concentration → Concentrated liquid (semi-finished product) → Dried finished product. Effectively retains active substances, improving yield.
Ethanol Recovery Process: Waste ethanol solution → Preheating → MVR evaporation → Ethanol vapor condensation → Recovery of high-purity ethanol. Ethanol recovery rate can reach over 90%, significantly reducing raw material costs.
High-Salinity Wastewater Zero Discharge Process: Pharmaceutical wastewater → Pretreatment (softening/oxidation/filtration) → MVR evaporation and concentration → Crystallization separation → Drying and salt extraction, distilled water reuse. Salt recovery, near-zero wastewater discharge, meeting the strictest environmental protection requirements.
IV. Case Studies and Results
Antibiotic Manufacturers: Using MVR evaporators to concentrate yeast broth reduces active ingredient loss by 50%, lowers operating costs by 40%, and significantly improves product yield.
Chemical Pharmaceutical Plants: Using MVR to recover ethanol generates millions of yuan in annual recovery value, with a payback period of 2-3 years.
Industrial Park Pharmaceutical Wastewater Treatment Plant: Achieves "zero discharge" of wastewater, with a distilled water reuse rate exceeding 95%, significantly reducing sewage discharge fees and environmental risks.
V. Application Challenges and Countermeasures
High Boiling Point Rise/High Viscosity Materials: Utilize forced circulation evaporators and optimize heat exchange design to avoid scaling and clogging.
Cross-contamination of Complex Components: Enhanced cleaning and separate treatment, employing dedicated equipment or isolated processes.
High Initial Investment: Conduct a comprehensive economic evaluation considering long-term operating costs, resource recovery benefits, and policy subsidies.
VI. Development Trends
Integration of Intelligent and Digital Factories: Remote monitoring, adaptive control, and big data-driven optimized operation.
Green Pharmaceuticals and Circular Economy: Strengthen resource recovery and zero emissions to contribute to sustainable development.
Modular and customized equipment: rapid delivery and flexible expansion meet the diverse needs of pharmaceutical companies.
Conclusion: MVR evaporators have fundamental and crucial application value in solution concentration, solvent recovery, and wastewater treatment in the pharmaceutical industry. Through scientific selection, process optimization, and intelligent operation and maintenance, they can significantly improve production efficiency, product quality, and environmental protection levels, providing solid technical support for pharmaceutical companies to reduce costs, increase efficiency, and achieve green transformation.
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