200 Ton Air Cooled Chiller 66-260 kW Cooling Capacity for Industrial Cooling Needs

Product Overview

Chiller

1. 1. 1. Maintain a constant temperature and humidity environment in the cleanroom to meet the stringent requirements of ISO cleanroom classification and process production for temperature and humidity (e.g., electronic chip workshops, biopharmaceutical cleanrooms);
      2. Provide process cooling for process equipment (e.g., lithography machines, fermentation tanks) to prevent equipment overheating from affecting precision or product quality;
      3. Cooperate with the HVAC system to achieve heat balance, reduce cleanroom energy consumption and improve system operation efficiency.

Features at a Glance

• Precise Regulation of Cleanroom Temperature and Humidity
• Targeted Cooling for Process Equipment
• Ensuring Stability of Cleanroom Pressure Differential
• System Energy Consumption Optimization and Energy-saving Operation
• Dual Protection for Processes and Environment

Typical Applications

• Pharmaceutical Cleanrooms
  Meets the needs of GMP-compliant HVAC systems.
• Electronics Manufacturing
  Supplies a stable environment for manufacturing.
• Medical Device Production
  Aids in maintaining controlled process environments.
• Laboratory Facilities
  Serves temperature-sensitive research operations.
• Cosmetic Production Areas
  Used within controlled manufacturing workshops.

Technical Specifications

Main Specification for Chiller

Cleanrooms typically require multiple, independent water systems with precise temperature control.

Note:A single chiller may serve one loop,or dual-temperature chillers may supply both chilled and reheat water simultaneously.

HVAC System Integration

It can be integrated with the following cleanroom systems:

• Air Handling Units (AHU)
• Fan Filter Units (FFU)
• Ducting Systems
• Air Distribution Networks
• Building Management Systems (BMS)
• Temperature and Humidity Control Systems

This helps establish stable environmental control for cleanroom facilities.

Engineering Process

SHP supplies engineering support through all phases of the project lifecycle:

• Requirement Analysis
  Check cooling load and cleanroom requirements.
• System Design
  Engineer HVAC cooling solutions based on the given project specifications.
• Equipment Manufacturing
  Manufacture and inspect equipment ahead of shipment.
• Installation Support
  Aid on-site installation and commissioning activities.
• Performance Verification
  Contribute to system testing and operational verification.

Related Cleanroom Projects

Related Project Track Record

Pharmaceutical Cleanroom Project – Mauritius

Scope: HVAC system design, chilled water loop integration and installation support.

Electronics Manufacturing Cleanroom

Scope: Cooling system design, integration of AHUs and environmental control support.

Validation & Testing

System Test & Verification

Prior to shipment, equipment may be tested through:

• Functional Testing
• Cooling Capacity Verification
• Electrical Safety Inspection
• Control System Testing
• Factory Acceptance Testing (FAT)

Actual testing procedures may vary to suit project requirements.

Certifications

Certifications

• ISO 9001:2015
• CE Certificates (if applicable)
• Cleanroom Related Testing Reports

Company Profile

Suzhou Huajing Air-Condition Purification Engineering Installation Co., Ltd. (SHP) provides cleanroom engineering, HVAC and environmental-control solutions for pharmaceutical, electronics, medical, laboratory and other controlled manufacturing facilities. The company was established in 2003 and provides design, manufacturing, installation, commissioning and validation support for cleanroom projects.

SHP reports more than 20 years of cleanroom engineering experience, 2,100+ completed projects and project delivery experience in more than 40 countries.

Our Certification

Why SHP

• More Than 20 Years of Cleanroom Engineering Experience
• 2,100+ Cleanroom Projects Finished
• Installations in Over 40 Countries
• Complete Design, Manufacturing, Installation and Validation Services
• Backing Pharmaceutical, Electronics, Laboratory and Medical Device Facilities

FAQ

Q1: Where is your company?

A1:Our company is located in Suzhou City, close to Shanghai. It's a 1.5-hour drive from PVG Airport.

Q2: Are you a manufacturer or a trading company? What can I buy from you?
A2: We are manufacturers. We focus on cleanroom projects, air showers, FFUs, through boxes, dosing rooms, laminar flow hoods and benches, AHUs, and sealed doors and Windows. 

Q3:When is your delivery time? 
A3: If your cleanroom project includes AHU, the delivery time is 35 days. If you purchase goods without an AHU, the delivery time is 10 days. 

Q4: How long is your warranty period? What kind of after-sales service can you offer?
A4: Our warranty period is two years after the completion of the project. During the warranty period, if there are any problems, we will replace it. If you can't handle it, we will send an engineer to solve it for free.

Q5:Can you conduct cleanroom validation? 
A5: Yes. We can provide DQ, IQ, OQ and PQ documentation, FAT/SAT reports, operation manuals, maintenance guides and complete cleanroom drawings according to project requirements. 

Q6:What are your advantages?
A6: We have a complete technical team consisting of 12 senior cleanroom and HVAC engineers to provide you with technical support. We have completed over 2,100 cleanroom projects in China and overseas. Such as Japan, Indonesia, Thailand, Bangladesh, India, North Macedonia, Saudi Arabia, Yemen, Russia, Moldova, Switzerland, Norway, the United Kingdom, Spain, France, Belgium, Kuwait, Tunisia, Mauritius, Sri Lanka, Mongolia, Philippines, Nepal, Sudan, Somaliland, Australia, New Zealand, Canada, Algeria, Egypt, Singapore, and the United States.