226300.pdf

Wichita KS VAMC May 22, 2020 VA Project No. 589-701 Bid Documents Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 1

SECTION 22 63 00

GAS SYSTEMS FOR LABORATORY AND HEALTHCARE FACILITIES

PART 1 - GENERAL

1.1 DESCRIPTION

A. Central Laboratory and Healthcare Gas Systems: Consisting of oxygen, nitrous oxide, nitrogen, and compressed air services; complete, ready for operation, including all necessary piping, fittings, valves, cabinets, station outlets, rough-ins, ceiling services, gages, alarms including low voltage wiring, nitrogen control panels, cylinder manifolds, air compressors, electric motors and starters, air dryers, filters, pressure regulators, dew point monitor, carbon monoxide monitor and all necessary parts, accessories, connections and equipment. Match existing station outlet and inlet terminal connections.

B. Laboratory and healthcare gas system alarm wiring from equipment to alarm panels.

C. A complete listing of all acronyms and abbreviations are included in

Section 22 05 11, COMMON WORK RESULTS FOR PLUMBING.

1.2 RELATED WORK

A. Section 01 00 00, GENERAL REQUIREMENTS.

B. Section 01 33 23, SHOP DRAWINGS, PRODUCT DATA, AND SAMPLES.

C. Section 01 81 13, SUSTAINABLE CONSTRUCTION REQUIREMENTS.

D. Section 01 91 00, GENERAL COMMISSIONING REQUIREMENTS.

E. Section 07 84 00, FIRESTOPPING: Sealing around pipe penetrations to maintain the integrity of time rated construction.

F. Section 07 92 00, JOINT SEALANTS: Sealing around pipe penetrations through the floor to prevent moisture migration.

G. Section 10 25 13, PATIENT BED SERVICE WALLS: Prefabricated bedside patient units (PBPU).

H. Section 13 05 41, SEISMIC RESTRAINT REQUIREMENTS FOR NON-STRUCTURAL

COMPONENTS: Seismic Restraint.

I. Section 22 05 11, COMMON WORK RESULTS FOR PLUMBING: General requirements and items common to more than one section of Division 22.

J. Section 22 05 12, GENERAL MOTOR REQUIREMENTS FOR PLUMBING EQUIPMENT:

Electric motors.

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 2

K. SECTION 22 08 00, COMMISSIONING OF PLUMBING SYSTEMS: Requirements for commissioning, systems readiness checklist, and training.

L. SECTION 22 62 00, VACUUM SYSTEMS FOR LABORATORY AND HEALTHCARE

FACILITIES: Vacuum Piping and Equipment.

M. Section 23 09 23, DIRECT-DIGITAL CONTROL SYSTEM FOR HVAC: Alarm interface with BAS.

N. Section 26 05 19, LOW-VOLTAGE ELECTRICAL POWER CONDUCTORS AND CABLES:

Control wiring.

O. Section 26 05 33, RACEWAY AND BOXES FOR ELECTRICAL SYSTEMS: Conduit.

P. Section 26 27 26, WIRING DEVICES: Electrical wiring and accessories.

Q. Section 26 29 11, MOTOR CONTROLLERS: Motor starters.

1.3 APPLICABLE PUBLICATIONS

A. The publications listed below form a part of this specification to the extent referenced. The publications are referenced in the text by the basic designation only.

B. American Society of Mechanical Engineers (ASME):

A13.1-2007 (R2013)......Scheme for the Identification of Piping Systems

B16.15-2013.............Cast Copper Alloy Threaded Fittings: Classes

125 and 250

B16.22-2013.............Wrought Copper and Copper Alloy Solder-Joint

Pressure Fittings

B16.50-2013.............Wrought Copper and Copper Alloy Braze-Joint

Pressure Fittings

B40.100-2013............Pressure Gauges and Gauge Attachments

ASME Boiler and Pressure Vessel Code -

BPVC Section VIII-2015..Rules for Construction of Pressure Vessels, Division I

BPVC Section IX-2015....Welding, Brazing, and Fusing Qualifications

C. American Society of Sanitary Engineers (ASSE):

6000 Series-2012........Professional Qualifications Standard for

Medical Gas Systems Personnel

D. American Society for Testing and Materials (ASTM):

B43-2014................Standard Specification for Seamless Red Brass

Pipe, Standard Sizes

B687-1999 (2011)........Standard Specification for Brass, Copper, and

Chromium-Plated Pipe Nipples

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 3

B819-2000 (R2011).......Standard Specification for Seamless Copper Tube for Medical Gas Systems

D1785-2012..............Standard Specification for Poly (Vinyl

Chloride) (PVC) Plastic Pipe, Schedules 40, 80, and 120

E. American Welding Society (AWS):

A5.8M/A5.8-2011.........Specification for Filler Metals for Brazing and

Braze Welding

B2.2/B2.2M-2010.........Specification for Brazing Procedure and

Performance Qualification

F. Compressed Gas Association (CGA):

C-9-2013................Standard Color Marking of Compressed Gas

Containers for Medical Use

G-4.1-2009..............Cleaning Equipment for Oxygen Service

V-1-2013................Standard for Compressed Gas Cylinder Valve

Outlet and Inlet Connections

G. Manufacturing Standardization Society (MSS):

SP-72-2010a.............Ball Valves With Flanged or Butt-Welding Ends

For General Service

SP-110-2010.............Ball Valves Threaded, Socket-Welding, Solder

Joint, Grooved and Flared Ends

H. National Electrical Manufacturers Association (NEMA):

ICS 6-1993 (R2001, R2006) Industrial Control and Systems Enclosures

I. National Fire Protection Association (NFPA):

99-2015.................Health Care Facilities Code

1.4 SUBMITTALS

A. Submittals, including number of required copies, shall be submitted in accordance with Section 01 33 23, SHOP DRAWINGS, PRODUCT DATA, AND

SAMPLES.

B. Information and material submitted under this section shall be marked

“SUBMITTED UNDER SECTION 22 63 00, GAS SYSTEMS FOR LABORATORY AND

HEALTHCARE FACILITIES”, with applicable paragraph identification.

C. Manufacturer's Literature and Data including: Full item description and optional features and accessories. Include dimensions, weights, materials, applications, standard compliance, model numbers, size, and capacity.

1. Piping.

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 4

2. Valves.

3. Inlet and outlet cocks

4. Valve cabinets.

5. Gages.

6. Station outlets and rough-in assemblies.

8. Alarm controls and panels.

9. Pressure Switches.

D. Station Outlets: Submit letter from manufacturer stating that outlets are designed and manufactured to comply with NFPA 99. Outlet shall bear label of approval as an assembly, of Underwriters Laboratories, Inc., or Associated Factory Mutual Research Corporation.

E. Certification: The completed systems have been installed, tested, purged, analyzed and verified in accordance with the requirements of this specification. Certification shall be submitted to COR.

F. Completed System Readiness Checklist provided by the CxA and completed by the contractor, signed by a qualified technician and dated on the date of completion, in accordance with the requirements of Section 22

08 00, COMMISSIONING OF PLUMBING SYSTEMS.

G. Submit training plans and instructor qualifications in accordance with the requirements of Section 22 08 00, COMMISSIONING OF PLUMBING

SYSTEMS.

1.5 QUALITY ASSURANCE

A. Materials and Installation: In accordance with NFPA 99 and as specified.

B. Equipment Installer: Show technical qualifications and previous experience in installing laboratory and healthcare equipment on three similar projects. Submit names, phone numbers, and addresses of referenced projects. Installers shall meet the qualifications of ASSE

Standard Series 6000.

C. Equipment Supplier: Provide evidence of equivalent product installed at three installations similar to this project that has been in satisfactory and efficient operation for three years. Submit names, phone numbers, and addresses where the product is installed.

D. Laboratory and healthcare System Testing Organization: The testing shall be conducted by a party technically competent and experienced in the field of laboratory and healthcare pipeline testing. Testing and systems verification shall be performed by personnel meeting the

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 5 qualifications of ASSE Standard Series 6000. Such testing shall be performed by a party other than the installing contractor.

E. Provide the names of three projects where testing of medical or laboratory gases systems has been performed by the testing agency.

Include the name of the project, names of such persons at that project who supervised the work for the project owner, or who accepted the report for the project owner, and a written statement that the projects listed required work of similar scope to that set forth in this specification.

F. Submit the testing agency's detailed procedure which shall be followed in the testing of this project. Include details of the testing sequence, procedures for cross connection tests, outlet function tests, alarm tests, purity tests, etc., as required by this specification. For purity test procedures, include data on test methods, types of equipment to be used, calibration sources and method references.

G. Certification: Provide COR documentation 10 working days prior to submitting request for final inspection to include all test results, the names of individuals performing work for the testing agency on this project, detailed procedures followed for all tests, and certification that all results of tests were within limits allowed by this specification.

H. “Hot taps” are prohibited for operating medical oxygen systems. Methods for connection and extension of active and pressurized medical gas systems without subsequent medical gas testing and verification are prohibited.

I. Bio-Based Materials: For products designated by the USDA’s Bio-

Preferred Program, provide products that meet or exceed USDA recommendations for bio-based content, so long as products meet all performance requirements in this specifications section. For more information regarding the product categories covered by the Bio-

Preferred Program, visit http://www.biopreferred.gov.

PART 2 - PRODUCTS

2.1 PIPING AND FITTINGS

A. Copper Tubing: Type "K", ASTM B819, seamless copper tube, hard drawn temper, with wrought copper fittings conforming to ASME B16.22 or brazing fittings complying with ASME B16.50. Size designated reflecting

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 6 nominal inside diameter. All tubing and fittings shall be labeled

"ACR/OXY", "OXY", "OXY/MED", "ACR/MED", or "MED".

B. Brazing Alloy: AWS A5.8M/A5.8, Classification BCuP, greater than 538 degrees C (1000 degrees F) melting temperature. Flux is strictly prohibited for copper-to-copper connections.

C. Threaded Joints: Polytetrafluoroethylene (Teflon) tape.

D. Underground Protective Pipe: Polyvinyl Chloride (PVC), ASTM D1785, Schedule 80.

E. Memory metal couplings: Temperature and pressure rating shall not be less than that of a brazed joint in accordance with NFPA 99, paragraph

5.1.10.6.1.

F. Apply piping identification labels at the time of installation in accordance with NFPA 99. Apply supplementary color identification in accordance with CGA Pamphlet C-9.

G. Special Fittings: The following special fittings shall be permitted to be used in lieu of brazed joints:

1. Memory-metal couplings having temperature and pressure ratings joints not less than that of a brazed joint.

2. Listed or approved metallic gas tube fittings that, when made up, provide a permanent joint having the mechanical, thermal, and sealing integrity of a brazed joint.

3. Dielectric fittings where required by the manufacturer of special medical equipment to electrically isolate the equipment from the piping distribution system.

4. Axially swaged, elastic strain preload fittings providing metal to metal seal having pressure and temperature ratings not less than that of a brazed joint and when complete are permanent and non-separable.

2.2 VALVES

A. Ball: In-line, other than zone valves in cabinets:

1. 75 mm (3 inches) and smaller: Bronze/ brass body, MSS SP-72, MSS

SP-110, Type II, Class 150, Style 1, with tubing extensions for brazed connections, full port, three-piece or double union end connections, Teflon seat seals, full flow, 4138 kPa (600 psig) WOG minimum working pressure, with locking type handle, cleaned for oxygen use and labeled for intended service.

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 7

2. 75 to 100 mm (3 to 4 inches): Bronze/ brass body, MSS SP-72 MSS

SP-110, Type II, Class 150, Style 1 with tubing extensions brazed to flanges, full port, three piece, double seal, Teflon seals, full flow, 4138 kPa (600 psig) WOG minimum working pressure, with locking type handle, cleaned for oxygen use and labeled for intended service.

B. Check:

1. 75 mm (3 inches) and smaller: Bronze/brass body, straight through design for minimum pressure drop, spring loaded, self-aligning with

Teflon cone seat, vibration free, silent operation, supplied NPT female threads at each end with flow direction arrow permanently cast into, cleaned for oxygen use and labeled for intended service, 2758 kPa (400 psig) WOG minimum working pressure.

2. 100 mm (4 inches) and larger: Iron body, bronze trim, swing type, vertical or horizontal installation, flange connection, with flow direction arrow permanently cast into, cleaned for oxygen use and labeled for intended service, 1035 kPa (150 psig) WSP.

C. Zone Valve in Cabinet: Ball valve, bronze/ brass body, double seal, three piece or double union end connections, replaceable Teflon seat seals, Teflon stem seal, 4138 kPa (600 psig) WOG, cold, non-shock gas working pressure service to 100 kPa (29 inches Hg), cleaned for oxygen use and labeled for intended service, blowout proof stem, one quarter turn of handle to completely open or close. Provide tubing extensions factory brazed, and pressure tested. Provide 3.2 mm (1/8 inch) NPT gauge port for a 50 mm (2 inch) diameter monitoring gauge downstream of the shut off valve. Zone valves shall be securely attached to the cabinet and provided with type “K” copper tube extensions for making connection to system piping outside the cabinet. Zone valves shall be products of one manufacturer, and uniform throughout in pattern, overall size and appearance. Trim with color coded plastic inserts or color coded stick-on labels. Install valves in cabinets such that cover window cannot be in place when any valve is in the closed position.

Color coding for identification plates and labels is as follows:

SERVICE LABEL IDENTIFICATION COLORS MFG. STD.

CLR.

OXYGEN White letters on green background GREEN

MEDICAL AIR Black letters on yellow background YELLOW

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 8

2.3 VALVE CABINETS

A. Flush mounted commercially available item for use with laboratory and healthcare services, not lighter than 1.3 mm (18 gage) steel or 1.9 mm

(14 gage) extruded aluminum, rigidly assembled, of adequate size to accommodate valve(s) and fittings. Punch or drill sides to receive tubing. Provide anchors to secure cabinet to wall construction. Seal openings in cabinet to be dust tight. Locate bottom of cabinet 1375 mm

(4 feet 6 inches) above finished floor.

B. Mount engraved rigid plastic identification plate on wall above or adjacent to cabinet. Color code identification plate to match gas identification colors as indicated above. Identification plate shall be clearly visible at all times. Provide inscriptions on plate to read in substance: "VALVE CONTROL SUPPLY TO ROOMS."

C. Cover plate: Fabricate from 1.3 mm (18 gage) sheet metal with satin chromed finish, extruded anodized aluminum, or 0.85 mm (22 gage) stainless steel. Provide cover window of replaceable plastic, with a corrosion resistant device or lever secured to window for emergency window removal. Permanently paint or stencil on window: CAUTION-CLOSE

ONLY IN EMERGENCY, SHUT-OFF VALVES FOR PIPED GASES", or equivalent wording. Configure such that it is not possible to install window with any valve in the closed position. Each valve shall have gauge upstream of valve inside valve box.

D. Cabinets and isolation valves shall be located and piped as shown on drawings, and at a minimum, so as to allow the isolation of each smoke compartment separately. No cabinet shall serve more than one smoke compartment.

2.4 GAGES

A. Pressure Gages: Includes gages temporarily supplied for testing purposes.

1. For line pressure use adjacent to source equipment: ASME B40.1, pressure gage, single, size 115 mm (4-1/2 inches), for compressed air, nitrogen and oxygen, accurate to within 2 percent, with metal case. Range shall be two times operating pressure. Dial graduations and figures shall be black on a white background, or white on a black background. Gage shall be cleaned for oxygen use, labeled for

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 9 appropriate service, and marked "USE NO OIL". Install with gage cock.

2. For all services downstream of main shutoff valve: Manufactured for oxygen use, labeled for the appropriate service and marked "USE NO

OIL", 40 mm (1-1/2 inch) diameter gage with dial range 1 to 690 kPa

(1 to 100 psig) for air service .

2.5 STATION OUTLETS

A. For all services : For designated service, consisting of a quick coupler and inlet supply tube. Provide coupler that is non-interchangeable with other services, and leak proof under three times the normal working pressure. Equip each station outlet with an automatic valve and a secondary check valve to conform with NFPA 99.

Equip each station inlet with an automatic valve to conform with NFPA

99. Place valves in the assembly to provide easy access after installation for servicing and replacement, and to facilitate line blow-out, purging, and testing. Fasten each outlet and inlet securely to rough-in to prevent floating and provide each with a capped stub length of 6 mm (1/4-inch) (10 mm outside diameter) (3/8-inch outside diameter) tubing for connection to supply. Identification of each gas service shall be permanently cast into the back plate and shall be visible through a transparent plastic guard. Label stub tubing for appropriate service. Rough-in kits and test plugs for PBPU are furnished under this specification but installed by manufacturer of

PBPU before initial test specified herein. Install completion kits

(valve body and face plate) for the remainder of required tests.

2.6 STATION OUTLETS

A. For all services: Brass, stainless steel or chromed metal non-interchangeable DISS connections for appropriate service to conform with CGA V-5. Equip each station outlet with an automatic valve and a secondary check valve to conform with NFPA 99. Equip each station inlet with an automatic valve to conform with NFPA 99. Place valves in the assembly to provide easy access after installation, for servicing and replacement, and to facilitate line blow-out, purging, and testing.

Fasten each outlet securely to outlet rough-in to prevent floating, and provide each outlet with a capped stub length of 6 mm (1/4-inch) (10 mm

(3/8-inch) outside diameter) tubing for connection to supply. Label stub tubing for appropriate service. Adjustable to compensate for

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 10 variations in plaster or cover thickness. Rough-in kits and test plugs for PBPU are furnished under this specification but installed by manufacturer of PBPU before initial tests specified herein. Install outlet completion kits (valve body and face plate) for the remainder of required tests.

2.7 STATION OUTLET ROUGH-IN

A. Anchor flush mounted rough-in securely to unit or wall construction.

B. Modular Cover Plate: Die cast back plate, two-piece 0.85 mm (22 gage) stainless steel or 1.6 mm (16 gage) chromium plated metal, with mounting flanges on all four sides, secured to rough-in with stainless steel or chromium plated countersunk screws.

C. Cover Plate for PBPU: One-piece with construction and material as indicated for modular cover plate.

D. Provide permanent, metal or plastic, identification plates securely fastened at each outlet and inlet opening, with inscription for appropriate service using color coded letters and background. Metal plates shall have letters embossed on baked-on enamel background. Color coding for identification plates is as follows:

SERVICE LABEL IDENTIFICATION PLATE COLORS

OXYGEN White letters on green background and vice versa

MEDICAL AIR Black letters on yellow

2.8 ALARMS

A. Alarm Panels:

1. General: Modular design, easily serviced and maintained; alarms operate on alternating current (AC) low voltage control circuit;

provide required number of transformers for efficient functioning of complete system. Alarm panels shall be integral units, reporting oxygen, compressed air and vacuum services, as required.

2. Box: Flush mounted, sectional or one piece, corrosion resistant.

Size box to accommodate required number of service functions for each location, and for one audible signal in each box. Anchor box securely. Provide spare capacity to accommodate 50 percent of the number of provided alarm points.

3. Cover plate: Designed to accommodate required number of signals, visual and audible, for each location, and containing adequate

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 11 operating instructions within the operator's view. Bezel shall be extruded aluminum, chromium plated metal, or plastic. Secure to the box with chromium plated or stainless steel countersunk screws.

4. Service indicator lights: Red translucent plastic or LED with proper service identification inscribed thereon. Number of lights and service instruction shall be as required for each location. Provide each panel with a green test button of the same material, inscribed with "PUSH TO TEST" or similar message.

5. Audible signal: Provide one in each alarm panel and connect electrically with all service indicator light functions.

6. Controls:

a. Visual signal: When the condition occurs which any individual service indicator light is to report, button for particular service shall give a lighted visual signal which cannot be canceled until such condition is corrected.

b. Audible signal: Alarm shall give an audible signal upon circuit energization of any visual signal. Audible signal shall be continuous until silenced by pushing a button. This shall cancel and reset audible only, and not affect the visual signal. After silencing, subsequent alarms shall reactivate the audible alarm.

c. Signal tester: Test button or separate normal light shall be continuously lighted to indicate electrical circuit serving each individual alarm is energized. Pushing test button shall temporarily activate all visual signals and sound audible signal, thereby providing desired indications of status of system.

PART 3 - EXECUTION

3.1 INSTALLATION

A. Open ends of tube shall be capped or plugged at all times or otherwise sealed until final assembly to prevent infiltration of any foreign matter.

B. Cut piping square and accurately with a tube cutter (sawing is prohibited) to measurements determined at place of installation. Ream tube to remove burrs, being careful not to expand tube, and so no chips of copper remain in the tube. Work into place without springing or forcing. Bottom tube in socket so there are no gaps between tube and fitting. Exercise care in handling equipment and tools used in cutting or reaming of tube to prevent oil or grease being introduced into

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 12 tubing. Where contamination has occurred, material is no longer suitable for oxygen service.

C. Spacing of hangers: NFPA 99.

D. Rigidly support valves and other equipment to prevent strain on tube or joints.

E. While being brazed, joints shall be continuously purged with oil free nitrogen. The flow of purged gas shall be maintained until joint is cool to touch.

F. Do not bend tubing. Use fittings.

G. Support ceiling column assembly from heavy sub-mounting castings furnished with the unit as part of roughing-in. Anchor with 15 mm

(1/2-inch) diameter bolts attached to angle iron frame supported from structural ceiling, unless otherwise indicated.

H. Provide two 25 mm (1 inch) minimum conduits from ceiling column assembly to adjacent corridor, one for mass spectrometer tubing and wiring and one for monitor wiring, for connection to signal cabling network.

I. Install pressure switches, transmitter and gauges to be easily accessed, and provide access panel where installed above plaster ceiling. Install pressure switch and sensors with orifice nipple between the pipe line and switches/sensors.

J. Apply pipe labeling during installation process and not after installation is completed. Size of legend letters shall be in accordance with ASME A13.1.

K. Pipe compressor intake to a source of clean ambient air as indicated in

NFPA 99.

L. After initial leakage testing is completed, allow piping to remain pressurized with testing gas until testing agency performs final tests.

M. Penetrations:

1. Fire Stopping: Where pipes pass through fire partitions, fire walls, smoked partitions, or floors, install a fire stop that provides an effective barrier against the spread of fire, smoke and gases as specified in Section 07 84 00, FIRESTOPPING, with intumescent materials only. Completely fill and seal clearances between raceways and openings with the fire stopping material.

2. Waterproofing: At floor penetrations, completely seal clearances around the pipe and make watertight with sealant as specified in

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 13

Section 07 92 00, JOINT SEALANTS. Bio-based materials shall be utilized when possible.

N. Provide 40 mm (1-1/2 inch) diameter line pressure gage downstream of zone valve in cabinets.

O. Provide zone valves in cabinets where indicated and outside each

Operating Room and a minimum one zone valve assembly for each 18 outlet set.

3.2 STARTUP AND TESTING

A. Initial Tests: Blow down and high and low pressure leakage tests as required by NFPA 99 with documentation.

B. Laboratory and/or healthcare testing agency shall perform the following:

1. Perform and document all cross connection tests, labeling verification, supply system operation, and valve and alarm operation tests as required by, and in accordance with NFPA 99 and the procedures set forth in pre-qualification documentation.

2. Verify that the systems, as installed, meet or exceed the requirements of NFPA 99, this specification, and that the systems operate as required.

3. Piping purge test: For each positive pressure gas system, verify cleanliness of piping system. Filter a minimum of 1000 liters (35 cubic feet) of gas through a clean white 0.45 micron filter at a minimum velocity of 100 liters per minute (3.5 SCFM). Filter shall show no discoloration, and shall accrue no more than 0.1 mg

(0.0000035 ounces) of matter. Test each zone at the outlet most remote from the source. Perform test with the use of an inert gas as described in CGA P-9.

4. Piping purity test: For each positive pressure system, verify purity of piping system. Test each zone at the most remote outlet for dew point, carbon monoxide, total hydrocarbons (as methane), and halogenated hydrocarbons, and compare with source gas. The two tests shall in no case exceed variation as specified in paragraph, “Maximum Allowable Variation”. Perform test with the use of an inert gas as described in CGA P-9.

5. Outlet and inlet flow test:

a. Test all outlets for flow. Perform test with the use of an inert gas as described in CGA P-9.

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 14

b. Oxygen, nitrous oxide and air outlets shall deliver 100 Lpm (3.5

SCFM) with a pressure drop of no more than 34 kPa (5 psig), and static pressure of 345 kPa (50 psig).

c. Nitrogen outlets shall deliver 565 Lpm (20 SCFM) with a pressure drop of no more than 34 kPa (5 psig), and static pressure of 1448 kPa (210 psig).

d. Needle valve air outlets shall deliver 1.5 SCFM with a pressure drop of no more than five psig, and static pressure of 345 kPa

(50 psig).

6. Source Contamination Test: Analyze each pressure gas source for concentration of contaminants, by volume. Take samples for air system test at the intake and at a point immediately downstream of the final filter outlet. The compared tests shall in no case exceed variation as specified in paragraph “Maximum Allowable Variation”.

Allowable concentrations are below the following:

Dew point, air 4 degrees C (40 degrees F) pressure dew point at 690 kPa (100 psig)

Carbon monoxide, air 10 mg/L (ppm)

Carbon dioxide, air 500 mg/L (ppm)

Gaseous hydrocarbons as methane, air

25 mg/L (ppm)

Halogenated hydrocarbons, air

2 mg/L (ppm)

7. Analysis Test:

a. Analyze each pressure gas source and outlet for concentration of gas, by volume.

b. Make analysis with instruments designed to measure the specific gas dispensed.

c. Allowable concentrations are within the following:

1) Laboratory air 19.5 percent to 23.5 percent oxygen.

Oxygen >=97% plus oxygen

Medical air 19.5% to 23.5% oxygen

8. Maximum Allowable Variation: Between comparative test results required are as follows:

Dew point 2 degrees C (35 degrees F)

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 15

Carbon monoxide 2 mg/L (ppm)

Total hydrocarbons as methane

1 mg/L (ppm)

Halogenated hydrocarbons

2 mg/L (ppm)

C. The CxA will observe startup and contractor testing of selected equipment. Coordinate the startup and contractor testing schedules with the COR and CxA. Contractor shall provide a minimum of 10 working days prior to startup and testing.

3.3 CONNECTION TO EXISTING LABORATORY GAS SYSTEM:

A. Contactor shall test the existing system for hydrocarbons, dew point, etc. per NFPA 99. If problems are present, the COR would notify the facility of the results. The facility would then make the necessary repairs and/or maintenance prior to connecting to new system.

B. Install shut-off valve at the connection of new line to existing line.

C. Time for shutdown of the existing laboratory and healthcare system shall be coordinated at least 10 work days prior to shutdown with the

COR and VA Medical Center.

D. Shut off all oxygen zone valves and gas riser valves if the section to be connected cannot be totally isolated from the remainder of the system.

E. Prior to any work being done, check the new pipeline for particulate or other forms of contamination per NFPA 99.

F. Ensure that the correct type of pipe tubing and fittings are being used.

G. Make a spot check of the existing pipelines in the facility to determine the level of cleanness present.

H. Reduce the pressure to zero and make the tie-in as quickly as possible.

A nitrogen purge is not required since this would require another opening in the pipe.

I. After the tie-in is made and allowed to cool, slowly bleed the source gas back into the pipeline. Test the work area for leaks with soapy water and repair any leaks.

J. After all leaks, if any, are repaired and the line is fully recharged, perform blow down and testing. Open the zone that is closest to the main to the system, access the closest outlet to the work, and blow the

Construct & Renovate Med/Surg Beds for Patient Privacy VKMR19

09-01-15

22 63 00 - 16 main through the outlet. After the outlet blows clear into a white cloth, make an additional check at a zone most distant from the work.

Perform all required NFPA 99 tests after connection.

3.4 COMMISSIONING

A. Provide commissioning documentation in accordance with the requirements of Section 22 08 00, COMMISSIONING OF PLUMBING SYSTEMS.

B. Components provided under this section of the specification will be tested as part of a larger system.

3.5 DEMONSTRATION AND TRAINING

A. Provide services of manufacturer’s technical representative for four hours to instruct VA Personnel in operation and maintenance of units.

B. Submit training plans and instructor qualifications in accordance with the requirements of Section 22 08 00, COMMISSIONING OF PLUMBING

SYSTEMS.

- - - E N D - - -