SECTION 22 61 19 Compressed-Air Equipment For Laboratory and Healthcare Facilities
SECTION 22 61 19 Compressed-Air Equipment For Laboratory and Healthcare Facilities
SECTION 22 61 19 Compressed-Air Equipment For Laboratory and Healthcare Facilities
SECTION 22 61 19
PART 1 - GENERAL
A. Drawings and general provisions of the Contract, including General and Supplementary
Conditions and Division 01 Specification Sections, apply to this Section.
1.2 SUMMARY
A. Section Includes:
1.3 DEFINITIONS
A. Actual Air: Air delivered at air-compressor outlet. Flow rate is compressed air delivered and
measured in acfm.
C. Low Voltage: As defined in NFPA 70 for circuits and equipment operating at less than 50 V or
for remote-control, signaling power-limited circuits.
D. Medical Air Equipment: Compressed-air equipment and accessories for healthcare facilities.
E. Standard Air: Free air at 68 deg F and 1 atmosphere before compression or expansion and
measured in scfm.
1.5 SUBMITTALS
A. Product Data: For each type of product indicated. Include rated capacities, operating
characteristics, electrical characteristics, and furnished specialties and accessories.
E. Operation and Maintenance Data: For compressed-air equipment to include in operation and
maintenance manuals.
A. Installer Qualifications:
B. Testing Agency Qualifications: An independent testing agency, with the experience and
capability to conduct the compressed-air equipment testing indicated, that is a member of the
Medical Gas Professional Healthcare Organization or is an NRTL and that is acceptable to
authorities having jurisdiction.
1. Qualify testing personnel according to ASSE 6020 for inspectors and ASSE 6030 for
verifiers.
C. Electrical Components, Devices, and Accessories: Listed and labeled as defined in NFPA 70,
by a qualified testing agency, and marked for intended location and application.
D. ASME Compliance: Fabricate and label receivers to comply with ASME Boiler and Pressure
Vessel Code.
E. Comply with NFPA 99, "Health Care Facilities," for compressed-air equipment and accessories
for medical air systems.
F. Comply with UL 544, "Medical and Dental Equipment," for medical compressed-air equipment.
1.7 COORDINATION
PART 2 - PRODUCTS
B. Control Panels: Automatic control station with load control and protection functions. Comply
with NEMA ICS 2 and UL 508.
C. Receivers: Steel tank constructed according to ASME Boiler and Pressure Vessel Code:
Section VIII, Division 1.
C. Air Compressor(s): Single-stage, oil-free, rotary, helical-screw type with nonlubricated helical
screws and lubricated gearbox, and of construction that prohibits oil from entering compression
chamber.
4. Capacity Control: Capacity modulation between 0 and 100 percent air delivery, with
operating pressures between 50 and 100 psig . Include necessary control to hold
constant pressure. When air demand is zero, unload compressor by using pressure
switch and blowdown valve.
5. Mounting: Freestanding.
D. Sound-attenuation enclosure.
E. Capacities and Characteristics: See Medical Air Compressor Schedule on the drawings.
B. Description: Twin-tower unit with purge system, mufflers, and capability to deliver plus 10
deg F 100-psig air at dew point. Include dew point controlled purge, step-down transformers,
disconnect switches, inlet and outlet pressure gages, thermometers, automatic controls, and
filters.
2.4 MOTORS
A. Comply with NEMA designation, temperature rating, service factor, enclosure type, and
efficiency requirements for motors specified in Division 22 Section "Common Motor
Requirements for Plumbing Equipment."
1. Motor Sizes: Minimum size as indicated. If not indicated, large enough so driven load
will not require motor to operate in service factor range above 1.0.
2. Controllers, Electrical Devices, and Wiring: Comply with requirements for electrical
devices and connections specified in Division 26 Sections.
A. Description:
1. Wall mounting.
2. Welded steel with white-enamel finish.
3. Gasketed door.
4. Grounding device.
5. Factory-installed signal circuit boards.
6. Power transformer.
7. Circuit breaker.
8. Wiring terminal board.
9. Internal wiring capable of interfacing 20 alarm signals.
PART 3 - EXECUTION
3.1 PREPARATION
A. Clean compressed-air equipment, accessories, and components that have not been cleaned for
oxygen service and sealed or that are furnished unsuitable for medical air applications,
according to CGA G-4.1, "Cleaning Equipment for Oxygen Service."
3.3 CONNECTIONS
A. Comply with requirements for water-supply piping specified in Division 22 Section "Domestic
Water Piping." Drawings indicate general arrangement of piping, fittings, and specialties.
B. Comply with requirements for drain piping specified in Division 22 Section "Sanitary Waste and
Vent Piping." Drawings indicate general arrangement of piping, fittings, and specialties.
F. Connect water supply to compressed-air equipment that requires water. Include backflow
preventer. Backflow preventers are specified in Division 22 Section "Domestic Water Piping
Specialties."
3.4 IDENTIFICATION
B. Identify medical compressed-air equipment system components. Comply with requirements for
identification specified in Division 22 Section "Identification for Plumbing Piping and Equipment."
and comply with NFPA 99.
3. Equipment Verification: Comply with requirements in ASSE 6020, ASSE 6030, and
NFPA 99 for verification of medical compressed-air equipment.
4. Replace damaged and malfunctioning controls and equipment.
5. Testing Certification: Certify that specified tests, inspections, and procedures have been
performed and certify report results. Include the following:
a. Inspections performed.
b. Procedures, materials, and gases used.
c. Test methods used.
d. Results of tests.
C. Components will be considered defective if they do not pass tests and inspections.
3.7 DEMONSTRATION
END OF SECTION 22 61 19