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SERVISOL

ELECTUS DISTRIBUTION NA1000 ELECTRONIC FREEZER
SPRAY
ChemWatch Full Report (REVIEW)
CHEMWATCH 4509-24
Date of Issue: Fri 27-7-2007


DISTRIBUTOR

Electus Distribution Pty Ltd
100 Silverwater Road
Silverwater NSW 2128
Phone: 02 9741 8555 Fax: 02 9741 8535




STATEMENT OF HAZARDOUS NATURE

Not classified as hazardous according to Worksafe Australia criteria.


CHEMWATCH HAZARD RATINGS

Flammability: 0
Toxicity: 2
Body Contact: 0
Reactivity: 0
Chronic: 0
SCALE: Min/Nil=0 Low=1 Moderate=2 High=3 Extreme=4




PERSONAL PROTECTIVE EQUIPMENT FOR INDUSTRIAL/COMMERCIAL
ENVIRONMENTS

Short Gloves
Goggles
Overalls
Half Face Respirator


MATERIAL DETAILS
CAS RN No(s): None
NIOSH No: None
UN No: 1950
DANGEROUS G. CLASS: 2.2
SUB RISK: None
PACKING GROUP: None
POISONS SCHEDULE: None
EPG: 2D1
IERG: 49
IMO CLASS: 2.2
IMDG PAGE: 2102
HAZCHEM: 2Y
LABEL: Non-flamm.Comp.Gas[2]




SHIPPING NAME

AEROSOLS


USE

Used to Freeze electronic parts.


APPEARANCE

Clear, colourless liquefied gas with slight ethereal odour; does not mix
with water. Supplied in aerosol pack.


PHYSICAL PROPERTIES

Molecular Weight: Not applicable.
Boiling Range (掳C): -26
Melting Range (掳C): Not available.
Specific Gravity (water=1): 1.21
Solubility in water (g/L): Immiscible
pH (as supplied): Not applicable
pH (1% solution): Not applicable.
Vapour Pressure (kPa): Not available
Volatile Component (%vol): 100
Evaporation Rate: Fast
Relative Vapour Density (air=1): 3.5
Flash Point (掳C): Not applicable
Lower Explosive Limit (%): Not applicable
Upper Explosive Limit (%): Not applicable
Autoignition Temp (掳C): Not available
Decomposition Temp (掳C): Not available.
State: Liquid


INGREDIENTS
NAME CAS RN %
tetrafluoroethane 811-97-2 >60
NOTE: Manufacturer has supplied full ingredient
information to allow CHEMWATCH assessment.




SYNONYMS

dust remover tetrafluoroethane 1,1,1,2-terafluoroethane
R 134A Fluorocarbon 134a HFC 134a HFA 134a



HEALTH HAZARD



ACUTE HEALTH EFFECTS

SWALLOWED

Considered an unlikely route of entry in commercial/industrial environments
Overexposure is unlikely in this form.
The liquid is harmful if swallowed and is capable of causing severe cold burns


EYE

The vapour is non-irritating to the eyes
The liquid is capable of causing severe cold burns


SKIN

Vapourising liquid causes rapid cooling and contact may cause cold burns,
frostbite.


INHALED

Material is highly volatile and may quickly form a concentrated atmosphere in
confined or unventilated areas. Vapour is heavier than air and may displace and
replace air in breathing zone, acting as a simple asphyxiant. This may happen
with little warning of overexposure.
Symptoms of asphyxia (suffocation) may include headache, dizziness, shortness
of breath, muscular weakness, drowsiness and ringing in the ears. If the
asphyxia is allowed to progress, there may be nausea and vomiting, further
physical weakness and unconsciousness and, finally, convulsions, coma and
death. Significant concentrations of the non-toxic gas reduce the oxygen level
in the air. As the amount of oxygen is reduced from 21 to 14 volume %, the
pulse rate accelerates and the rate and volume of breathing increase. The
ability to maintain attention and think clearly is diminished and muscular
coordination is somewhat disturbed. As oxygen decreases from 14-10% judgement
becomes faulty; severe injuries may cause no pain. Muscular exertion leads to
rapid fatigue. Further reduction to 6% may produce nausea and vomiting and the
ability to move may be lost. Permanent brain damage may result even after
resuscitation at exposures to this lower oxygen level. Below 6% breathing is in
gasps and convulsions may occur. Inhalation of a mixture containing no oxygen
may result in unconsciousness from the first breath and death will follow in a
few minutes.
WARNING:Intentional misuse by concentrating/inhaling contents may be lethal.


CHRONIC HEALTH EFFECTS

Principal routes of exposure are usually by inhalation of vapour/spray mist and
skin contact / eye contact
As with any chemical product, contact with unprotected bare skin; inhalation of
vapour, mist or dust in work place atmosphere; or ingestion in any form, should
be avoided by observing good occupational work practice.


FIRST AID

SWALLOWED

If swallowed do NOT induce vomiting.
If vomiting occurs, lean patient forward or place on left side (head-down
position, if possible) to maintain open airway and prevent aspiration.
Observe the patient carefully.
Never give liquid to a person showing signs of being sleepy or with reduced
awareness; i.e. becoming unconscious.
Give water to rinse out mouth, then provide liquid slowly and as much as
casualty can comfortably drink.
Seek medical advice.


EYE

If this product comes in contact with the eyes:
Immediately hold eyelids apart and flush the eye continuously with running
water.
Ensure complete irrigation of the eye by keeping eyelids apart and away from
eye and moving the eyelids by occasionally lifting the upper and lower lids.
Continue flushing until advised to stop by the Poisons Information Centre or a
doctor, or for at least 15 minutes.
Transport to hospital or doctor without delay.
Removal of contact lenses after an eye injury should only be undertaken by
skilled personnel.


SKIN

If skin or hair contact occurs:
Flush skin and hair with running water (and soap if available).
Seek medical attention in event of irritation.
In case of cold burns (frost-bite):
Bathe the affected area immediately in cold water for 10 to 15 minutes,
immersing if possible and without rubbing.
DO NOT apply hot water or radiant heat.
Apply a clean, dry dressing.
Transport to hospital, or doctor.


INHALED

If fumes or combustion products are inhaled remove from contaminated area.
Lay patient down. Keep warm and rested.
Prostheses such as false teeth, which may block airway, should be removed,
where possible, prior to initiating first aid procedures.
Apply artificial respiration if not breathing, preferably with a demand valve
resuscitator, bag-valve mask device, or pocket mask as trained. Perform CPR if
necessary.
Transport to hospital, or doctor, without delay.


ADVICE TO DOCTOR

Treat symptomatically.




TOXICITY AND IRRITATION

No data for Zeus Dust Away.

TETRAFLUOROETHANE:
No significant acute toxicological data identified in literature search.




PRECAUTIONS FOR USE



EXPOSURE STANDARDS

No data for Zeus Dust Away.




EXPOSURE STANDARDS FOR MIXTURE

"Worst Case" computer-aided prediction of vapour components/concentrations:

Composite Exposure Standard for Mixture (TWA) (mg/m鲁): 4240 mg/m鲁
If the breathing zone concentration of ANY of the components listed below is
exceeded, "Worst Case" considerations deem the individual to be over
overexposed.
Component Breathing Zone ppm Breathing Zone mg/m鲁 Mixture Conc: (%)
tetrafluoroethane 1000 4240 100




INGREDIENT DATA

TETRAFLUOROETHANE:
ES TWA: 1000 ppm, 4240 mg/m鲁
OES TWA: 1000 ppm, 4240 mg/m鲁
Studies show that HFC 134a is practically nontoxic by inhalation. The
acute lethal effects occur at levels exceeding 500000 ppm whilst the
threshold for cardiac sensitisation occurs at about 75000 ppm. Repeated
exposures at 50000 ppm for 13 weeks did not produce significant toxicity
in animals. Limited studies have shown the substance not to be a
carcinogen, or to exhibit mutagenic effects. Exposures up to 300000 ppm
and 40000 ppm did not produce teratogenic effects in rats and rabbits
respectively. The workplace environmental exposure level (WEEL),
recommended by the AIHA, is thought to be protective against cardiac
sensitisation and systemic injury.




ENGINEERING CONTROLS

Use in a well-ventilated area
General exhaust is adequate under normal operating conditions. If risk of
overexposure exists, wear SAA approved respirator. Correct fit is essential to
obtain adequate protection. Provide adequate ventilation in warehouse or closed
storage areas. Air contaminants generated in the workplace possess varying
"escape" velocities which, in turn, determine the "capture velocities" of fresh
circulating air required to effectively remove the contaminant.

Type of Contaminant: Air Speed:
solvent, vapours, degreasing etc., 0.25-0.5 m/s (50-100 f/min)
evaporating from tank (in still air)
aerosols, fumes from pouring 0.5-1 m/s (100-200 f/min.)
operations, intermittent container
filling, low speed conveyer transfers,
welding, spray drift, plating acid
fumes, pickling (released at low
velocity into zone of active
generation)
direct spray, spray painting in 1-2.5 m/s (200-500 f/min)
shallow booths, drum filling, conveyer
loading, crusher dusts, gas discharge
(active generation into zone of rapid
air motion)
grinding, abrasive blasting, tumbling, 2.5-10 m/s (500-2000 f/min.)
high speed wheel generated dusts
(released at high initial velocity
into zone of very high rapid air
motion).

Within each range the appropriate value depends on:

Lower end of the range Upper end of the range
1: Room air currents minimal or 1: Disturbing room air currents
favourable to capture
2: Contaminants of low toxicity or of 2: Contaminants of high toxicity
nuisance value only
3: Intermittent, low production. 3: High production, heavy use
4: Large hood or large air mass in 4: Small hood - local control only
motion

Simple theory shows that air velocity falls rapidly with distance away from the
opening of a simple extraction pipe. Velocity generally decreases with the
square of distance from the extraction point (in simple cases). Therefore the
air speed at the extraction point should be adjusted, accordingly, after
reference to distance from the contaminating source. The air velocity at the
extraction fan, for example, should be a minimum of 1-2 m/s (200-400 f/min.)
for extraction of solvents generated in a tank 2 meters distant from the
extraction point. Other mechanical considerations, producing performance
deficits within the extraction apparatus, make it essential that theoretical
air velocities are multiplied by factors of 10 or more when extraction systems
are installed or used.




PERSONAL PROTECTION



EYE

No special equipment for minor exposure i.e. when handling small quantities.
OTHERWISE: Safety glasses with side shields.
Contact lenses pose a special hazard; soft lenses may absorb irritants and all
lenses concentrate them.




HANDS/FEET

No special equipment needed when handling small quantities.
OTHERWISE: Wear general protective gloves, eg. light weight rubber gloves. Or
as required: Wear chemical protective gloves, eg. PVC. Wear safety footwear.




OTHER

No special equipment needed when handling small quantities.
OTHERWISE:
Overalls.
Barrier cream.
Eyewash unit.
DO NOT spray on hot surfaces.




RESPIRATOR

Respiratory protection may be required when ANY "Worst Case" vapour-phase
concentration is exceeded (see Computer Prediction in "Exposure Standards").

Protection Factor Half-Face Respirator Full-Face Respirator
5 x ES Air-line* AX-2
- AX-PAPR-2
10 x ES - AX-3
10+ x ES - Air-line**
* - Continuous Flow; ** - Continuous-flow or positive pressure demand
^ - Full-face

The local concentration of material, quantity and conditions of use determine
the type of personal protective equipment required. For further information
consult site specific CHEMWATCH data (if available), or your Occupational
Health and Safety Advisor.




HANDLING PROCEDURES
Avoid all personal contact, including inhalation.

Wear protective clothing when risk of exposure occurs.

Use in a well-ventilated area.

Prevent concentration in hollows and sumps.

DO NOT enter confined spaces until atmosphere has been checked.

Avoid smoking, naked lights or ignition sources.

Avoid contact with incompatible materials.

When handling, DO NOT eat, drink or smoke.

DO NOT incinerate or puncture aerosol cans.

DO NOT spray directly on humans, exposed food or food utensils.

Avoid physical damage to containers.

Always wash hands with soap and water after handling.

Work clothes should be laundered separately.

Use good occupational work practice.

Observe manufacturer's storing and handling recommendations.

Atmosphere should be regularly checked against established exposure standards

to ensure safe working conditions are maintained.




CONDITION CONTRIBUTING TO INSTABILITY
Elevated temperatures.

Presence of open flame.

Product is considered stable.

Hazardous polymerisation will not occur.
SAFE HANDLING



STORAGE

SUITABLE CONTAINER

Aerosol dispenser. Check that containers are clearly labelled.




STORAGE INCOMPATIBILITY

Avoid reaction with alkali metals, magnesium and magnesium alloys, zinc,

aluminium alloys ( > 2% magnesium).

Avoid contact with plastics such as methacrylate polymers, polyethylene and

polystyrene.




STORAGE REQUIREMENTS

Store in original containers.

Store in an upright position.

DO NOT store in pits, depressions, basements or areas where vapours may be

trapped.

No smoking, naked lights, heat or ignition sources.

Keep containers securely sealed.

Contents under pressure.

Store in a cool, dry, well ventilated area; away from incompatible materials.

Avoid storage at temperatures higher than 40 deg C.

Protect containers against physical damage.

Check regularly for leaks.

Observe manufacturer's storing and handling recommendations.




TRANSPORTATION
Class 2.2 - Non-flammable gases shall not be loaded in the same vehicle or
packed in the same freight container with:

Class 1 - Explosives;

Class 4.2 - Spontaneously combustible substances;

Class 5.2 - Organic peroxides.




SPILLS

MINOR SPILLS

Clean up all spills immediately.

Avoid breathing vapours and contact with skin and eyes.

Wear protective clothing, impervious gloves and safety glasses.

Shut off all possible sources of ignition and increase ventilation.

Wipe up.

If safe, damaged cans should be placed in a container outdoors, away from all

ignition sources, until pressure has dissipated.

Undamaged cans should be gathered and stowed safely.




MAJOR SPILLS

Clear area of personnel and move upwind.

Alert Fire Brigade and tell them location and nature of hazard.

May be violently or explosively reactive.

Wear breathing apparatus plus protective gloves.

Prevent, by any means available, spillage from entering drains or water courses

No smoking, naked lights or ignition sources.

Increase ventilation.

Stop leak if safe to do so.

Water spray or fog may be used to disperse / absorb vapour.

Absorb or cover spill with sand, earth, inert materials or vermiculite.

If safe, damaged cans should be placed in a container outdoors, away from

ignition sources, until pressure has dissipated.

Undamaged cans should be gathered and stowed safely.
Collect residues and seal in labelled drums for disposal.




PROTECTIVE ACTIONS FOR SPILL


>From IERG (Canada/Australia)
Isolation Distance -
Downwind Protection Distance 8 metres




FOOTNOTES
1 PROTECTIVE ACTION ZONE is defined as the area in which people are at risk
of harmful exposure. This zone assumes that random changes in wind direction
confines the vapour plume to an area within 30 degrees on either side of the
predominant wind direction, resulting in a crosswind protective action distance
equal to the downwind protective action distance.
2 PROTECTIVE ACTIONS should be initiated to the extent possible, beginning with
those closest to the spill and working away from the site in the downwind
direction. Within the protective action zone a level of vapour concentration
may exist resulting in nearly all unprotected persons becoming incapacitated
and unable to take protective action and/or incurring serious or irreversible
health effects.
3 INITIAL ISOLATION ZONE is determined as an area, including upwind of the
incident, within which a high probability of localised wind reversal may
expose nearly all persons without appropriate protection to life-threatening
concentrations of the material.
4 SMALL SPILLS involve a leaking package of 200 litres (55 US gallons) or less,
such as a drum (jerrican or box with inner containers). Larger packages leaking
less than 200 litres and compressed gas leaking from a small cylinder are also
considered "small spills".
LARGE SPILLS involve many small leaking packages or a leaking package of
greater than 200 litres, such as a cargo tank, portable tank or a "one-tonne"
compressed gas cylinder.
5 Guide 126 is taken from the US DOT emergency response guide book.
6 IERG information is derived from CANUTEC - Transport Canada.




DISPOSAL
Consult State Land Waste Management Authority for disposal.

Discharge contents of damaged aerosol cans at an approved site.

Allow small quantities to evaporate.

DO NOT incinerate or puncture aerosol cans.

Bury residues and emptied aerosol cans at an approved site.
FIRE FIGHTERS' REPORT




EXTINGUISHING MEDIA

Water spray or fog.

Foam.

Dry chemical powder.

BCF (where regulations permit).

Carbon dioxide.




FIRE FIGHTING

Alert Fire Brigade and tell them location and nature of hazard.

May be violently or explosively reactive.

Wear breathing apparatus plus protective gloves.

Prevent, by any means available, spillage from entering drains or water

courses.

Use fire fighting procedures suitable for surrounding area.

DO NOT approach containers suspected to be hot.

Cool fire exposed containers with water spray from a protected location.

If safe to do so, remove containers from path of fire.

Equipment should be thoroughly decontaminated after use.

When any large container (including road and rail tankers) is involved in a fire,

consider evacuation by 100 metres in all directions.




FIRE/EXPLOSION HAZARD

Non combustible.

Not considered to be a significant fire risk.

Heating may cause expansion or decomposition leading to violent rupture of

containers.

Aerosol cans may explode on exposure to naked flames.
Rupturing containers may rocket and scatter burning materials.

Hazards may not be restricted to pressure effects.

May emit acrid, poisonous or corrosive fumes.

Decomposes on heating and may emit toxic fumes of carbon monoxide (CO).

If involved in fire emits toxic fumes of fluorides




FIRE INCOMPATIBILITY

Avoid reaction with alkali metals, magnesium and magnesium alloys,

zinc, aluminium alloys ( > 2% magnesium).




ENVIRONMENTAL
No data for Freezer Spray.

Refer to data for ingredients, which follows:



TETRAFLUOROETHANE:



Persistence and Degradation:

Decomposed comparatively rapidly in the lower atmosphere (troposphere).

Atmospheric lifetime is 15.6 years. Products of decomposition will be

highly dispersed and hence will have a very low concentration. Does not

influence photochemical smog (i.e. is not a VOC under the terms of the

UNECE agreement). Does not deplete ozone.

Effect on Effluent Treatment:

Discharges of the product will enter the atmosphere and will not result in

long term aqueous contamination. [ICI]




CONTACT POINT
AUSTRALIAN POISONS INFORMATION CENTRE
24 HOUR SERVICE: 13 11 26
POLICE, FIRE BRIGADE OR AMBULANCE: 000
NEW ZEALAND POISONS INFORMATION CENTRE
24 HOUR SERVICE: (03) 4747 000
NZ EMERGENCY SERVICES: 111




End of Report



Issue Date: Fri 27-7-07



Print Date: Fri 27-7-07



This document is copyright. Apart from any fair dealing for the purposes of

private study, research, review or criticism, as permitted under the Copyright

Act, no part may be reproduced by any process without written permission from

CHEMWATCH. TEL (+61 3) 9572 4700.

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