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Horizontal Flow MVR Evaporator With 316L Material and CIP System for Pharmaceutical Industry Steam Heating 120°C

Horizontal Flow MVR Evaporator With 316L Material and CIP System for Pharmaceutical Industry Steam Heating 120°C photo-1
Horizontal Flow MVR Evaporator With 316L Material and CIP System for Pharmaceutical Industry Steam Heating 120°C photo-2
Horizontal Flow MVR Evaporator With 316L Material and CIP System for Pharmaceutical Industry Steam Heating 120°C photo-3
Horizontal Flow MVR Evaporator With 316L Material and CIP System for Pharmaceutical Industry Steam Heating 120°C photo-4
Horizontal Flow MVR Evaporator With 316L Material and CIP System for Pharmaceutical Industry Steam Heating 120°C photo-5

Product Spotlights

Horizontal flow MVR evaporator with 316L material and CIP system for pharmaceutical steam heating at 120°C. Energy-saving design, low fouling, GMP-compliant. Customizable capacity (500-10,000 L/h). Integrated CIP reduces downtime. Backed by ISO-certified manufacturer with global export experience (US$10M-$50M/year).
US$ 8900 - 889000 MOQ: 3 Combos
Key Specifications
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Material:
Other, 316L Stainless Steel
Certification:
Other, ISO9001
Heating Method:
Steam Heating
Payment & Shipping
Payment Methods:
Port of Shipment:
Qingdao
Delivery Detail:
30 days
Material Other, 316L Stainless Steel
Certification Other, ISO9001
Heating Method Steam Heating
Operating Temperature 120°C
Flow Type Horizontal Flow
CIP System Integrated CIP System
Application Industry Pharmaceutical Industry
Evaporator Type Mechanical Vapor Recompression (MVR)

As a leading manufacturer specialized in environmental and pharmaceutical equipment, Qingdao Conqinphi Environmental Technology Group Co., Ltd. (established 2015, factory size 10,000-30,000 sqm) proudly presents the Horizontal Flow MVR Evaporator with 316L Material and CIP System. This advanced evaporation solution is designed for the pharmaceutical industry, utilizing steam heating at 120°C to efficiently concentrate heat-sensitive solutions while minimizing energy consumption. Our unit integrates a clean-in-place (CIP) system for hygienic operation, meeting the strictest demands of GMP and pharmaceutical manufacturing. With over 200 employees and annual export value exceeding US$10 million, we deliver reliable, high-performance equipment trusted by clients across North America, Europe, and Asia.

This evaporator combines mechanical vapor recompression (MVR) technology with a horizontal flow design, offering superior heat transfer and low fouling. The use of 316L stainless steel ensures excellent corrosion resistance and compatibility with pharmaceutical-grade liquids. The integrated CIP system allows efficient cleaning without disassembly, reducing downtime and ensuring batch-to-batch consistency. Below we detail the key features, technical specifications, and benefits.

Key Features & Advantages

  • Energy Efficiency: MVR technology recycles latent heat from vapor, cutting steam consumption by up to 90% compared to traditional single-effect evaporators.
  • 316L Material: Full wetted parts are made of 316L stainless steel, offering high resistance to chlorides, acids, and alkaline cleaning agents.
  • CIP System: Automatic clean-in-place with programmable cycles; no manual dismantling required, enhancing hygiene and reducing maintenance.
  • Horizontal Flow Design: Minimal product hold-up volume, shorter residence time, and lower temperature differentials – ideal for heat-sensitive pharmaceutical products.
  • Steam Heating at 120°C: Stable and controllable heating source; temperature can be precisely regulated for different concentration levels.
  • Compact Footprint: Horizontal configuration saves vertical space, suitable for cleanroom or limited-height installations.
  • GMP-Compliant Design: Smooth internal surfaces, no dead legs, full weld penetration, and easy validation support.

Technical Specifications

Parameter Value / Option
Model CQ-MVR-HF-316L series
Evaporation Capacity 500 – 10,000 L/h (customizable)
Operating Temperature Up to 120°C (steam heating)
Material of Construction 316L stainless steel (wetted parts)
Compressor Type Centrifugal / Roots (optional)
CIP System Integrated with spray balls and programmable logic controller
Heating Source Saturated steam (pressure adjustable)
Control System PLC + HMI touch screen, remote monitoring optional
Power Supply 380V / 50Hz (3-phase) or customized
Certifications ISO9001, ISO14000, OHSAS18001, HACCP, SA8000, and more

Beyond these specifications, the unit can be tailored with optional features such as automatic condensate recovery, vacuum operation for lower boiling points, and explosion-proof electrical components for solvent applications.

Client Benefits

  • Reduced Operating Costs: Energy savings of 60–80% compared to traditional evaporators; less steam consumption means lower utility bills.
  • Enhanced Product Quality: Gentle evaporation at low delta-T prevents thermal degradation of APIs and excipients.
  • Hygiene and Compliance: CIP system eliminates manual cleaning; 316L material resists corrosion and meets FDA/EU standards for pharmaceutical contact surfaces.
  • Scalability: We offer multiple capacity ranges to match batch sizes from pilot to full production; all units are fully tested before shipment.
  • Global Service: With a strong export track record (US$10M–US$50M/year), we provide installation guidance, spare parts, and online technical support.

Trust & Reliability

At Qingdao Conqinphi Environmental Technology Group, we have been manufacturing evaporation systems since 2015, occupying a 10,000–30,000 sqm factory with 201–300 skilled employees. Our products have been exported to all major global markets including North America, Europe, South America, and Asia. We are proud to hold multiple certifications: ISO9001, ISO14000, OHSAS18001, HACCP, TL900, QS9000, SA8000, and others that reflect our commitment to quality, environment, and social responsibility. Each Horizontal Flow MVR Evaporator is rigorously tested for leak-tightness, CIP functionality, and performance at 120°C steam heating. We offer a one-year warranty and fast after-sales response. Contact us today for a customized solution that fits your pharmaceutical concentration needs. Let our expertise help you achieve superior efficiency and compliance.

Frequently Asked Questions (FAQ)

  1. Q: What is the typical evaporation capacity of your Horizontal Flow MVR Evaporator for pharmaceutical use?
    A: Our standard models range from 500 L/h to 10,000 L/h. Capacity can be customized based on your feed volume and concentration requirements. Please provide your process parameters for a tailored quotation.
  2. Q: Can the evaporator handle solvents or flammable liquids?
    A: Yes, with optional explosion-proof design (EX-rated motors, sensors, and enclosures). We recommend discussing solvent handling needs with our engineers to ensure safe operation.
  3. Q: How does the CIP system work and what cleaning agents are recommended?
    A: The CIP system uses automatic spray balls to circulate cleaning solutions (e.g., 1–2% NaOH, then 0.5–1% HNO3, followed by rinse water). The cycles are programmable via PLC. We provide a standard cleaning protocol and can adapt to your SOPs.
  4. Q: What is the minimum operating temperature if I want to process heat-sensitive products?
    A: The steam heating system is designed for 120°C, but we can also integrate vacuum operation to lower boiling points (e.g., 50–80°C at reduced pressure). This is an available option for thermolabile substances.
  5. Q: Is the 316L material suitable for chloride-containing solutions (e.g., saline or buffers)?
    A: 316L offers good resistance to chlorides under typical pharmaceutical concentrations (e.g.,
  6. Q: Do you provide installation supervision or commissioning services?
    A: Yes, we offer on-site commissioning and training support for international clients. Our service team can travel to your facility, or we can guide you remotely via video calls. Spare parts are available from our Qingdao warehouse.
  7. Q: What certifications does your evaporator comply with?
    A: The unit is manufactured under ISO9001 quality management system, and we can provide material certificates (3.1), weld maps, FAT test reports, and other documentation required for pharmaceutical validation. Our company also holds ISO14000, OHSAS18001, HACCP, and other certifications.
  8. Q: How long is the lead time for a standard Horizontal Flow MVR Evaporator?
    A: Typically 45–60 days after order confirmation, depending on capacity and customizations. We can expedite for urgent projects upon request.
Product Tags: Horizontal Flow MVR Evaporator , 316L Steam Heated CIP Evaporator , Pharmaceutical MVR Evaporation System

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Gold Verified Supplier
1Yr
Verified Business License
Business Type
Manufacturer
Year Established
2015
Factory Size
10,000-30,000 square meters
Annual Export Value
US$10 Million - US$50 Million

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