Professional Documents
Culture Documents
Scope of work
Technical Specification
Liquid oxygen will be the primary(main) supply source and the oxygen manifold
will work as stand by. In case of failure in liquid oxygen supply, it should automatically
switch over to oxygen manifold.
The unit shall consist of a double walled vertical vessel(made of stainless steel and
carbon steel) for out door installation capacity 10,000 liter.
It should be fitted with standard accessosries as minimum and should have undergone
standard Inspection requirement. A certificate to that effect has to be submitted.
2. Oxygen Manifold
The manifold should be so designed that it shall suit easy cylinder changing and
positioning. The system should have non-return valves for easy changing of cylinders
without closing the bank.
The cylinder should be placed with the help of cylinder brackets and fixing chains which
should zinc plated.
The Oxygen Control Panel will be of Digital Type, fully Automatic and shall switch
from “Bank in U to “Reserve Bank” without fluctuation in delivery line pressure and
without the need for external electrical power. After the switch- over, the “Reserve
Bank” shall become the “Bank in Use” shall become the “Reserve Bank”. The Control
Panel will be powered by a microprocessor located behind the front door panel.
The Control Panel will have 3 large, red, illuminated LED displays, for the Left Bank, the
Right Bank and for Delivery Pressure. The control panel will also have Six LED’s, two
Green for “Bank in Use”, two Amber for “Bank Ready” and two red for “Bank Empty”.
All components inside the Control Panel like Pressure Regulators, piping and control
switching equipment shall be cleaned for Oxygen Service and installed inside the
cxabinet to minimize tampering with the regulators or switch settings.
The Control Panel shall include two pressure relief valves, one high pressure 200 psi and
one low pressure 75 psi.
The Control Panel will be made to provide Heavy Duty and have a Flow Capacity of over 2000
LPM.
The Vacuum Pump station should be stalk mounted with 4 identical pumps of > 2000
cfm capacity (oil seated rotary vein cooled vacuum pumps) with on line starter and pump
protection filters. Each Vacuum Pump will be complete with Base Plate, Belt Guard, V
Belts, Motor and Starter. The system should be of Automatic Start and Stop Type with
standard filter.
The pumps should have integral, fully recirculating oil supply with sight to indicate oil
level. The oil separation system shall consist of no less than four stages of internally
installed oil and smoke eliminators. This system shall be capable of removing 99.9 % of
oil and smoke particles from the exhaust.
Provide audible and visual local alarm (complete with indicating lights) for vacuum
pump thermal malfunction and reserve vacuum pump in use.
The Pumps should be connected to common vertical receiver of 4000 liters capacity. The
receiver shall have a drain valve at the bottom and indigenous.
5. Air Compressors.
The package shall include Tripex oil-less air compressors and associated
equipment one vertical ASME tank and one dupex control panel. The entire
system including the receiver shall be mounted on a common structural steel stack
base. All components shall be completely pre-piped and pre- wired to single –
point service connections. An interconnecting piping and wiring shall be
completed and operationally tested prior to shipment.
The medical air compressor shall be of the totally oil –less reciprocating air-
cooled design. Connecting rod and bearing shall be packed with lifetime
lubrication and sealed
The system shall include individual compressor inline filters, discharge check
valve of bronze construction, safety relief valves, bronze intake and discharge
flexible connectors solenoid unloaders, isolation valves, air cooled after coolers
for each compressor, high discharge temperature shut down switches on each
cylinder, pressure control switches, as well as copper tubing with shut- of cock for
gauge and switches.
The storage tank shall be equipped with a pressure gauge, safety relief valve, 3-
way by-pass; gauge glass and automatic electronic tank drain with manual
override. The inside of the tank shall be coated for rust protection.
Dual desiccant air dryers, dual 0.5 micron pre- filters, dual 0.5 micron after-
filters, line pressure regulating valves, dew point monitor, CO monitor and other
accessories required to meet and exceed the current code requirements shall be
mounted on the compressor system base. All components shall be completely pre-
paid and pre- wired to single- point service connections as per latest NFPA/
international standards.
There shall be two identical banks of air treatment equipment, piped in parallel
and provided with valves to by-pass either filter set for element replacement,
maintenance and repair work on one of the sets while still treating medical
compressed air through the other set without any sacrifice in air quantity. Each
bank should consist of three stages of treatment.
The first stage is a prime efficiency coaleser with particle removal down to 0.5
micron with 99.9999% retention. This filter removes aerosol and solid particles.
The filter is equipped with electron drain and element change indicator.
The second stage is a desiccant heatless air dryer, equipped with purge control.
Built-in purge saver control will automatically minimize and adjust the amount of
purge air to match the variable airflow. The dry compressed air is discharged
from “on line” tower into the third stage.
The third stage is a prime efficiency particulate after filter with particle removal down to 0.5
micron. The after filter element is provides high retention, low-pressure drop and long
element life.
Downstream pressure regulators will maintain constant discharge pressure of 55 PSIG (field
adjustable).
Digital dew point and CO monitors with alarm set points at +39 º F and 10 PPM are
provided with dry contacts for connection to remote alarm panels. A “demand check” for
maintenance should as per current code requirements of latest NFPA/ international standards.
6. Distribution piping
Copper pipes should be solid drawn, seamless, deoxidized, non arsenical, half hard, tempered
and degreased copper pipe conforming to standards BS EN 1057. All copper pipes should be
degreased & delivered capped at both ends. The pipes should be accompanied with
manufacturers test certificate for the physical properties & chemical composition. Copper
pipe will also have reputed third party inspection certificate (eg. Lloyd’s).
Fittings shall be made of copper and suitable for a steam working Pressure of 17 bar and
especially made for brazed socket type connectors.
The isolation Valves will be made of Chromium plated brass and Non Lubricated Ball type.
All Valves shall be pneumatically tested for twice the working pressure and Factory
Degreased for medical gas service.
Installation of piping shall be carried out with utmost cleanliness. Only pipes, fittings and
valves that have been degreased and fittings brought in polythene sealed bags shall be used at
site. Pipe fixing clamps shall be of nonferrous or non-deteriorating plastic suitable for all
diameter of the pipe.
All pipe joints shall be made using flux less brazing method. All joints shall be made of copper-
to copper and brazed by silver brazing filler material without flux.
Adequate supports shall be provided while laying pipelines to ensure that the pipes do not sag.
Suitable sleeves shall be provided wherever pipes cross through walls/ slabs. All pipe clamps
shall be non- reactive to copper.
After erection, the pipes will be flushed with dry nitrogen gas and then pressure tested with dry
nitrogen at a pressure equal to twice the working pressure or 150 psig, whichever is higher for a
period of not more than 24 hours.
All the piping system shall be tested in the presence of the site-engineer or his authorized
representative.
Painting
All exposed pipes should be painted with two coats of synthetic enamel paint and color
codification should be as per IS: 2379 of 1963.
Valve boxes
The valve box shall be constructed of 18 gauge complete with baked off finish.
The doorframe assembly shall be constructed of anodized aluminum and shall mounted
to the back box assembly by screws as provided. The removable front consist of a clear
window with a pullout ring pre- mounted to the centre of the window.
Each recessed zone valve box shall consist of the following components. A steel box
which can house single or multiple shut-off ball valves with tube extension. A piece
design Valve, an aluminum frame, and a pull-out removable window.
Valves shall be a 4- bolt design, bronze body, double seal, union ball-type, with (TFE)
seats and Viton seals, “O” ring packing, and ball which seals in both direction blow-out
proof stem, with a pressure rating of 2760 kPa (400 psig). Valves shall operated by a
lever –type handle requiring only a quarter turn from a fully open position a fully
closed stub extension of sufficient length to protrude beyond the sides of the box.
Each valve shall be supplied with an identification bracket bolted directly onto the
body for the purpose of applying an approved medical gas identification label. A pack
of labels shall be supplied with each valve box assembly for application by the
installation.
Valves shall be available with line pressure gauges, as required. Gauges shall be (2”)
diameter, with metal case and ring.
Pressure gauge shall read 0-700 kPa (0-100 psig) for all except nitrogen, which shall
read 0-2000 kPa (0-3000 psig), and vacuum, which shall read -100-0 kPa (o-30” Hg.
7. Alarm System
The alarm will be of modular construction and Digital Type and consist of master alarm and area
alarms at various locations.
The alarms shall be microprocessor based with individual microprocessors on each display and
sensor board. The sensors shall be capable of local or remote mounting. Each sensor and display
units shall be specific, with an error message display for an incorrect connection.
The alarms shall be field expandable with the addition of extra modules. Up to six services can
be accommodated per standard box.
Each specific service shall be provided with an LED digital readout comprising of 0-250 psi for
positive pressure and 0-30 inch Hg for Vacuum. The digital readout shall provide a constant
indication of each service being measured. A bar graph trend indicator shall be provided for each
service indicating a green “NORMAL”. Yellow “CAUTION” and a red “HIGH” or “LOW”
alarm condition. Under normal operation the bar graph display shall move up and down in the
green range depending on service usage. If an alarm occurs, the “RED” alarm light will flash and
the audible alarm will sound. Pushing the “ALARM SILENCE” button will cancel the audible
alarm, but the unit will remain in the alarm condition until the problem is rectified.
The default set points shall be +/- 20 % variation from normal condition.
In addition “PUSH TO TEST” & “ALARM SILENCE” buttons shall be easily accessible to
operate and test the unit.
Combination master/ area alarms shall have no moving parts and shall require no maintenance
after initial installation.
8. Pendants
The single arm ceiling pendant with movable arm up to 330º shall be of pneumatically /
electrically operated type.
The pendant shall be at a height of 180 cm from the floor at its lowest position after
installing.
All electric and medical gas services shall be provided to the lower section by means of
flexible hoses and cables. All threaded connections will comply with NFPA
recommendations preventing interchange of connections.
Some OT’s like cardiac and neuro OT should have surgeons pendants as well with
additional facility like
º Electrocautery
º selves
The ICU pendant should be of single arm with Horizontal movement up to 300º
with shelves for ventilator and monitor
Provision for 5 gas outlets, 8 electrical outlets, selves with drawer system and side
rails,
Examination lamp and basket for suction catheters and monitor cables.
Quadruple infusion management system
The Bed Head Panel shall be constructed out of extruded aluminum profiles
with power coating. The Bed Head Panel shall house gas outlets and electrical sockets &
switches.
Segregation of Services i.e. electrical and medical gases shall be maintained throughout
as per standard.
• Gas Outlets:
Outlets shall be manufactured with a 165 mm long Copper inlet pipe stub which is silver brazed
to the outlet body. The inlet pipe stub should be capable of swiveling by 360 degrees. Body
shall be 33 mm diameter one-piece brass construction.
For positive pressure gas services, the outlet shall be equipped with a primary and secondary
check valve and the secondary check valve shall be rated at minimum 200 psl in the event the
primary cjeck valve is removed for maintenance.
Outlet bodies shall be gas specific by indexing each gas service to a gas specific dual pin
indexing arrangement on the respective identification modula.
A large colour-coded front plate shall be used for ease of gas identification and aesthetic appeal.
With the back bow mounted the outlet shall adjust up to 19 mm variation in mounting palte
thickness.
The latch valve assembly should accept only corresponding gas specific adaptors.
All outlets shall be cleaned and degreased for medical gas service, factory assembled and tested.
Back Pressure Compensated flow meter will be of accurate gas flow measurement with
following features:
Ward Vacuum Unit will be of light weight and compact. The unit will consist of
A regulator,