Hazardous Chemical Awareness Flashcards

1
Q

Hazard Communication Standard (HCS)

A

OSH Act addresses the protection of workers from chemicals in the workplace. HCS CFR 29 - 1910.1200 in 1983 and expanded it to overall workers in 1987. The HCS necessitates employers to evaluate chemical hazards in their facilities and to communicate the hazard information to their employees.

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2
Q

HCS Program

A
Steps for the HCSP HCP in writing
perform a chemical inventory
File Must have SDS for each chemical
Label all containers and storage areas containing chemicals
train employees
make the HCP available in writing
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3
Q

Safety Data Sheet

A
A written document for SDS written doc specific info on defined hazardoouse chemicals and effects
the united nations global harmonization standard GHS
16 sections
1. identification
2. Hazard identifications
3.Composition and ingredients
4 First aid measures
5 fire fighting measures
6. accidental release measures
7 handling and storage
8. Exposure controls
9 physical and chemical properties
10. stability and reactivity
11.  Toxicological information
12 ecological information
13 disposal information
14 transport information
15 Regulatory information
16 Other information
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4
Q

Additonal information

A

in addition the MSDS the HCS requires that every container of hazardous materials is labeled by the manurfacturer - the DOT places plackers on bulk packages alerting handlers of the contents. hazard warnings and the name and address of the manufacturer
labels must provide the chemical identiry of the hazardous material hazard warnings
the data helps employees
to ensure the safety of themselves and others in the workplace.

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5
Q

Labeling

A

Labeling and plackarding is often considered the quickest source of information
HCS requires to be labeled by the manufacturer
must contain chemical identity and or trade name of the hazardous material, Hazard warnings or warnings
name and address of the chemical manufacturer

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6
Q

Plackarding

A

is a system of hazard warning required by the DOT
are placed on bulk packages such as portable tanks and transportating vehicles carrying hazardous materials durieng transit
labels are smaller in size and are required on non bulk packages such as boxes and cannisters
many employers find the labels to be convenient for marking materials within their facilities

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7
Q

National Fire Protection System NFPA 704 singing system

A

Is designed to provide possible chemical risks to emergeny and first responders
Rating
1. health
2. Flammability
3. Reactivity
4th - Special Hazard
an area of the sign - any special hazard
Local fire codes require facilities to post on doors warning that dangerous chemicals are within.. In addition to package lables To post the signs on buildings and doors to warn that dangerous chemicals are within.
many employers add small adhesive labels using the NFPA design. these provide addition ways of warning employees

It is important to remember that the Hazard Communication Standard applies to hazardous chemicals that are being used in a facility, not to hazardous waste. Therefore, waste site workers use labels, placards, and signs as a source of information, not identification.

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8
Q

Chemical Names w/ Potential Hazards

A

terms can be very confusing and misleading.
Toxic or non-toxic compound. Spill response workers cannot assume the hazard of any chemical - verify all information
Name
Hazard must be verified

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9
Q

Verification

A
Verification can come from . . .
Label
SDS 
Refereence books
Technical Specialists

Chemist should be available to assist in spill Clean up if the hazards cannot be confirmed staff must us maximum protective equipment and caution.

name is looked at before the label or sds
the presence of certain elements in the chemical name suggests the presence of possible hazards.

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10
Q

Potentially Hazardous elements

A

Potential hazardous elements list - filed.

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11
Q

Names of Elements

A

The presence of certain words and word fragments can show possible hazards. Not every chemical compound that containg name or framents are that end
ite
ate
ade
ide
Not every word that contains that fragment is hazardous chemical.

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12
Q

Corrosive Health Hazards

A
sulfuric acid is the most common eg. - 2nd used transported hazardous materials. Only flamable liquids are more common.
corrosives are used in everything from batteriuas to disinfectants.  Must be able to identify corrosive class chemicals. Any liquid that can have severe a corrosive rate on steel.  
Because it can corrode steel it is possible to corrode other substances including human tissue.

2 types of corrosive materials that can corrode steel and human tissue.

acids of corrosives
bases or caustics

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13
Q

PH’s

A

PH is used when discussing acids or bases. PH is the negative log of the concentration of hydrogen in solution. When the concentration of hydrogen increase the PH #decreases. A PH of 11 is hydrogen ion concentration is very low.
Bases have very low hydrogen concentrations and high hydroxide concentrations. A liquid with a PH of 11 is a base.
PH can range from 0 to 14. Acids on the low end 0 to 7 and the Bases on the high end of 7 to 14.
Solutions with a PH of 7 are neutral.

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14
Q

Acid Base Neutralization

A

when dealing with corrosive or caustic spills the usual response with a neuralization reaction. If an acid is spilled it will be neutralized with a base - caustic. If a caustic - base is spilled, it will be neutralized with an acid.
Reaction of an acid and base it creates a toxic atmosphere. .
Lessen the possibilites of an uncontrolled reaction and avoid harmful situatiations. It is important to uderstand the neutralization process.

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15
Q

Mixing chemicals

A

when mixing acids and bases - 3 general products are formed
salt
water
heat
Energy is always produced Controlling the amount of heat energy produced is very important.
An understend in g of the terms is essential

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16
Q

Strength vs Concentration

A

Strong acids or bases - refering the concentration of the acidic or basic solution. Strength is defined as the % of dissociation that occurs when an acid or base is mixed with water.
how much the material solid or liquid come apart, dissociate in water to form electricly charged particles positive or negative ions. Acids diassociate to produce hydrogen ions and bases to produce hydroxide ions.
the greater disassociation increasing hydrogen or hydroxide the greateer the strength of the resulting or the base solution.

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17
Q

Concentration

A

Is defined as the amount of material acid or base mixed with a certain amount of water expressed in terms of %, weight or volume.
The more water by % the more dilute the solution. the less water added the more concentrated the solution.
if one has concentrated hydrodgen chloride = the liquid material has the maximum amount of hydrogen chloride dissolved in that amount of water.
To add more hydrogen chloride gas to the solution - no more would or could dissolve, It would just bubble through the liquid and escape

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18
Q

50% dilution

A

50% concentration of hydrogen chloride = given amount of the concentrated solution with equal amount of water. Comparing concentration of the pure solution to the 50% solution has only 1/2 of the # of hydrogen ions as the concentrated portion .
% and malarity are expressions that identify the concentration . Remember the larger the number before the term, the more concentrated the solution.

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19
Q

Corrosive Health Hazards

A

Corrosives can destroy living tissue. Chemical Burns. Some acids and bases can cause severe damage even with momentary exposure to the skin because they are so corrosive.

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20
Q

Vapor Hazards

A

The most dangerous hazard. Fuming liquids can spontaneously produce vapor.
if a vapor cloud is created large scale evacuation is required.
Injuries from vapors can be mucus membranes - Eyes , throat and airway, and Irritation is to the respiratiory system.
Vapor pressure is a liquid propertery At room temperature and sea level there is one atmosphere of pressurethat pushes down on a liquin in the container the as it boils it overcomes the pressure of the atmosphere and it escapes in gas form or vapor.. Materials with vapor pressure less than 1 will boil at room temperature. greater than 1 will remain liquid at room temperature.
a materials vapor pressure is crucial when responding to a materials release.

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21
Q

Liquid Hazards

A

Must be handled carefully to avoid splashing. Skin damage can be caused by contact with a liquid corrosive.

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22
Q

Solid Hazards

A

Dusts from solid corrosives can create produce severere damage to external and internal injuries organs. Massive Exposure to dusts from corrosives Can be fatal within a matter of minutes

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23
Q

Protective Measures

A

Safer to handle corrosive material if is preventative measures are taken first. PPE equipment. Glove for hands. Goggles for eyes. Face Shiled or work behind a splash shield. if working with acids or bases dont wear Contact lenses because they can become welded to the eye leading to blindness.

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24
Q

Treatment for exposure

A

Stopping the chemical action = flushing to flush out and neutralize the material. After flushing victim should be treated with standard first aid practices.
the extent of injury is dependant on the concentration of the acid or base, - the quantity, body area affected and the duration of contact.

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25
Q

Hazardous Mixtures

A

Mixing of chemicals. more so with corrosives. Used in everything from flash lights to car batteries.. Possiblle complications that could arise if corrosives are mixed with various types of materials.

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26
Q

Corrosives and poisons

A

cynide or sulfide salts the primary concern is the possible toxic vapors that can be produced by the decomposition of the poision.. The vapors can be more toxic than corrosives.

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27
Q

Corrosives and ignitable materials

A

flammable or combustible material. there are many possible reactions with the exact type dependent on the specific corrosive and flamable and or combustible material - egs of the hazards are when a strong base or acid is mixed with a polar or water soluable flamable or combustible liquid heat can be generated or this can be seen when water is added to an acid.

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28
Q

Increase in temperature

A

Because of the increase in temperature there will also be an increase in the amount of vapors generated by the liquid.
the liquid normally at the termp of the environment will be warmer than its environment.
eg. a liquid normally considered below its flashpoint. the temp at which enough vapor is produced for a fllash ignition to occur. May have been heated to a temperature above the flashpoint. THis means that if enought vapor is present and an ignition source is found a fire will result.

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29
Q

Corrosives and Metal

A

contact of Corrosive with a metal. Evident that one of the possible reactions is the destruction of the metal itself. ts is of great importance when the metal that it corrodes is in a container with the same metal that stores this chemical.

                                             The other type of reaction is the production of hydrogen gas.  THis can be expecially dangerous whey it occurs indoors.  Never charge a car battery indoors.
30
Q

Polychlorinated Biphenyls (PCBs)

A

Family 209 chlorinated isomers of Biphenyls. PCBs discovered in the late 19th Century - introduced into the US 1929 and in use since that time since this time in most industrial nations. they have chemical stability resistance to heat low flamability and high dialectic consistency.
Colorless viscous fluid is insoluable in water and can withstand high temps without degradation.
they are non bio degredable. The higher chlorinated isomers are not readily degraded.

31
Q

Additional info on PCB’s

A

transported in water. Are attracted to segments. uptake of PCB’s by plants. Poultry cattle and hogs - after the animals have eatenfeed contaminated with PCB’s . Detected in human fatty adipose tissues.

32
Q

Solvents

A

flammable liquid refers to any liquid having Flashpoint below 100oF or 37.8 Degree C

except any mixture having components with flashpoints of 100oF 37.8oC or higher
the total of which make up 99.9% or more of the total volume of the mixture.

The DOT and EPA define flammable liquid as a liquid with a flash point of less than 140oF.

33
Q

Flamable Solvents

A

have been in use for many years. The physical hazards to the workplace are in the form of Fire and explosion. Acetone, ether, hexane, toluene and ethanol, zylene are common flamable solvents.
Flammable solvents fire protection is a primary concern. The proper use of safety cans grounding and bonding and flamable storage cabinets is critical.

34
Q

Halogenated Solvents

A

Hydrocarbon solvents consist of 1 or more halogen atoms chlorene, Florene or Bromene
safety solvents used in the last 20 years
they do not flash or burn and have few acute health hazards and are at a Reasonable cost
Today the safety is being questioned.

35
Q

Flammabality

A

not a problem with halogenated solvents.
in a fire the bi products of decomposing halogenic solvents are deadly. chronic health problems due to inhalation and skin contact as well as an adverse effect on the environment. play a role in the depletion of the ozone layer and are listed as greenhouse gasses.
general halogenic solvents are the freon based solvents methalene chloride trichloroethylene and 111 trichloroethane

36
Q

Solvent Hazards

Explosion or Fire

A

the major hazard of flammable liquid solvents is the physical hazard of fire or explosion.

Flammability refers to the ability of a material to generate a high concentration of flammable vapors in an unconfined area under normal circumstances
3 factors necessary for a fire
1. fuel (something to burn)
2. an oxidizer to promote burning (oxygen source)
3. ignition source

37
Q

Flashpoint

A

the lowest temperature at which a liquid gives off enough vapor to form a flammable mixture with air.

flammable liquids OSHA and NFPA definition have a flashpoint below 100 o F Class 2 combuistible liquids are also hazardous - flashpoints are 100oF and 140oF.

DOT and EPA define flammable liquid as a liquid with a flashpoint below 140oF

38
Q

Ignition point

A

2 fuel oil 120oF high flash point and a lower ingition temperature of 650oF

the temperature that the vapor must reach in order to ignite.
There isn an inverse relationship between flashpoint adn the inigtion temperature. the higher the flashpoint the lower the ignition temp.
Gasoline has a low flashpoint -40oF and a high ignition temp. 850oF.

39
Q

LEL and UEL

A

minimum concentration of flammable liquid vapor in air necessary for a mixture to ignite is is called the lower explosive limit LEL anything below is too low to ignite.

the upper explosive limit UEL is the concentration of liquid vapor in the air that is too rich to ignite it will not burn because there is too little oxygen .

the vapor has displaced the oxygen and the oxygen concentration has dropped to less than 14%

the flammable or explosive range includes everything between the upper and lower explosive limits.

40
Q

Spills of flammable liquids

A

Spills on hot surfaces in a quantity that can reach the flammable range. management and er services should be notified. 1 or more gallons should bring this response.
Specific conditions may call for assistance with smaller spills.
A spill of flammable liquid into a sump or pit. Less than a gallon can create a afire hazard in a confined space.
You can detect their hazardous vapors by their smell.

41
Q

Safety Containers

A

Basic rules that we have a tendancy of pouring or mixing flamable materials in a close proximity to sparks or flammablehigh temperature areas. Theis is the worst possible situation - go out to a site and notice gas cans that are intended for personal and private use sat your home.
field and gas tanks - plastic containers are not appropriatae uel storage cans.

Should not be used to store flamable liquids.
Sturdy metal and long filter devise insitde the container that will prevent the fire into the container creating an explosion. A
Flame arrester used to stop the flamed

A spring loaded top - allows the air to escape reducing the pressure inside.
in another container
Also keep s the

42
Q

Static electricity and Ignightable

A

Flammable liquids can be ignited by sparks, matches, open flames other sources of ignition including static electricity.

Static electricity generated by contact and separation of dissimilar material. EG fluid flows thru a pipe or an orifice into a tank.

A point of danger from a static spark is the palce where flammable liquid or vapor may be present in the air. At a delivery hose nozzle into a container.

When the right vapor mixed with the right amount of air one little spark can cause an explosion with flammable liquids.

43
Q

Reducing Risk of Explosion

Bonding and Grounding

A

Bonding and Grounding.
Ground the container to a good ground or earth. A solid bare copper wire or other approved conductor going to a metal water pipe.

A good conductor wire would be placed so that there is a metal to metal connection and not to a painted surface and then the other end of the wire would placed on the other container metal to metal connection.
Any static electricity would then be dissipated to the grounding bonding wires to ground reducing the risk of static sparking.
Why don’t we have to do this when we fill our gas tanks at gas stations? because there is adequate bonding and grounding.

44
Q

Additional Safety Tips

A

Well Ventilated Storage areas - fumes and vaporsfrom flammables can create an explosion hazard. Accidental mixtures can create a hazard. Prevent.
Home heating fules cannot be mixed
Flammable liquids are more easily ignightable than combustible liquids.
Each liquid has specific uses it is import to read and understand everything that you use.. if you read the labels on the chemmicals you purchase for home use.
Pressureized spray paint can be hazardous if not used properly.
read understand and follow instructions on all chemicals because they can be hazardous when not used properly.
Take care of health and safety when using storing chemicals

45
Q

Flammable Liquid Vapors

A

Toxic below detection limit. explosive gas meters detect flammable liquids. Meters are not sensitive to all gasses. Any indication of flammable gas should be a concern.
Flammable ranges are in %s.
1% = 10,000 parts/million An explosive gasmeter cannot be used to detect gases at PEL levels concentrations are generally less than 1000 ppm or 0.1% of the total atmosphere.

The resulting hazard of flammable solvents and the primary hazard of other solvents are the health effects.

46
Q

Solvents Do’s and Donts

A
  1. Do use only approved and labeled containers for storing and transportation
  2. do make sure ther eis proper ventilation
  3. Do keep flammables away from heat and ignition sources
  4. Do check that containers and hoses are in proper working conditions.
  5. Ground, bond yourself and your work to avaoidtrnsfer of charge
  6. Dont mix solvents
  7. follow instructions & double check
  8. Don’t smoke eat or drink around hazardoun
  9. dont wear contact lenses around hazardous substances
  10. Dont track hazardous materials from one location to the next.
47
Q

Treatment for Solvent Exposure

A
  • Immediately call for help
  • move victim for fresh air and give cpr if necessary.
  • do not attempt to rescue if ther eis a chance that it is a solvent vapor without proper PPE
  • have a standby observer present
  • make sure the victim gets medical help
  • dont become part of the problem
  • never attempt rescue in a confined spave unless properly trained, equiped etc otherwise you can be come part of the problem
48
Q

Oxidizers

A

Any material that will gain electrons during a chemical reaction that stimulates the combustion of organic materials.
primary hazards are similar to those of oxidizing elements
they include:
intensification of combustion
spontaneous ignition
explosion
toxic fume production

49
Q

Hazards with oxidizing compounds

A

are similiar to oxidizing elements. Include
intensification of combustion
spontaneous ignition
explosion
and production of toxic fumes.
of these 4 hazards
spontaneous ignition is a causative hazard. Explosions may be causative or subsequent meaning they follow the cause of the cause of the incident.

50
Q

Intensification of Combustion

A

Oxidizer is the oxidizer intensifying combustion.
Rate of combustion increases as well as the heat of combustion. there is more fuel being oxidied than under normal conditions. The oxygen produced is greatly dependent on the heat exposure the greater the rate of the oxygen production this in turn produces more cpmmbustion and heat production.

51
Q

Spontaneous ignition

A

standard rules No longer apply in the presence of oxidiers. A material normally difficult to ignite may burst into flanes in an oxidizer enriched atmosphere.
because the flammable range and flashpoints used to measure the potential flamablaity are greatly modified

the oxidizer widens the material’s flammable range in an environment with 4 X the oxygen, the LEL is 4 times lower and UEL 4 times higher.

Oxidizer enriched atmosphere may contain oxygen, flourine, chlorene, or other oxidizers. Oxidizers do not burn but support and intensify combustion.

52
Q

Explosion

A

When oxygen is mixed with flammable materials such as solvents or gasoline. There is a serious fire or explosion as the decomposition accelerates additional heat is generated which helps the . decomposition rate.

The same for peroxides - pure peroxides are often explosive

53
Q

Toxic Fume Productin

A

The effect that inhalation of vapors and smoke have on the respiratory system. Both vapors and smoke dissolve in the mucus lining of the respiratory trat. and produce corrosive liquid that will damage the tissues of the respiratory tract.

It is important to examine the effect of various common extinguishing agents in fighting oxidizers fires because of the way oxidizers behave when involved in fire.
the best extinguishing agent is water there are hazards involved in using water -impregnation of combustibles, runoff and possible water reactivity of the oxidizer.

54
Q

Extinguishing agents for Oxidizers

A
The best extinguishing agent is water
Hazards involved are:
Impregnation of the combustibles
Runoff
Possible reactivity of the oxidizer
55
Q

Control and Stabalization

A

Water is a primary tool used in many er situation. Workers must refrain from using on water reactive materials.

Workers must refrain from using actions that will make a situation worse than better.
Large fires with water reactive it is best in most situatins to Reduce human exposure and let a fire burn

56
Q

Unstable materials

A

Substanstes that will spontaneously decompose polymerize or self react under shock temperature or pressure are called unstable materials.
A reactive hazardous material needs outside stimulus to react.
Unstable materials does not need outside stimilus to react.
Treat unstable materials as explosives unless otherwise proven. do not move or handle a material until its stability can be verified.

57
Q

Characteristics of Unstable Materials

A

Unstable Hazardous materials exist as liquids crystals or solids. Molecules with 2 or more atoms bonded together chemically of unstable materials it is found that Many of these share electrons in order to form molequeles or compounds the sharing of electrons between atoms is called covelant bonding forming or breaking bonds is easy.

Many unstable materials have bonds that are easy to form or break therefore it doesnt take much to set them off
Two groups unstable materials
Organic Peroxides
Monymers

58
Q

Control and Stabilization

A

treat unstable materials as explosives until proven otherwise. Do not move or handle material until its stability can be verified.
if you stumble accorss jars with chemicals or sealed 55 gal drums - walk lightly as these materials can be unstable.

some materials such as pitric acid can have unstable salts.
simply tapping on the container or using tools to open it can be extremely dangerous.

59
Q

Explosives

A

chemical compounds or mixtures of various compounds that are cabpable of undergoing rapid chemical changes with the simultaneous
large quantities of heat and gasses. this release of high heat causes the gasses to expand rapidly
the rapid expansion exerts the pressure causes shockwaves and a velocity that can exceed the speed of sound

60
Q

Explosive trains

A

a variety of shapes or forms. It may be a liquid,in a glass black powder in a pipe, a gel, a plastic. A rolled up cord, detonative cord, etc.
An explosive device contains fuel an oxidizer and a detonative device.
an explosive train
can be very complex and includes a number of variables and factors:
A primer
an igniter
a detonater
a booster charge
A main charge

61
Q

Safety fuse

A

A safety fuse attached to a blasting cap that is attached to a high explosive is an explosive train.

safety fuse is a textile cord that acts as an ignigter.
wrapped around the textile cord is black powder primes the balsting cap at the other end.

the blasting cap in turn detonates the main charge or the high explosive that is difficult to detonate.

booster is also a high explosive but is much more sensitive than the main charge.

62
Q

Primary and Secondary explosives

A

Primary are extremely sensitive to heat and shock . 2ndary high explosives are more stable. A small amount of primary explosive is used to detonate the larger amount of 2ndary in some devised.
A primary system employed by DOT

63
Q

DOT Classifications

A

Class 1
1.1 explosives with mass explosion hazard
1.2 with a projection hazard
1.3 a fire hazard
1.4 no significant blast hazard
1.5 vary insensitive
1.6 extremely insensitive explosive articles
Forbidden explosives are not allowed to be shipped by common carrier one additonal classification is for blasting agents which are a mixture of oxidizers + fuels and are insensitive to heat and shock.

64
Q

Purging

A

the removal of standing water surrounding a well in order to take proper sampling. Standard sop s will provided a nuber of well volumes that must be pruged out prior to sample collection to refresh the well. Then, the water level must be checked to ensure that the well has reharged and is full prior to sampling.

The purged water should be containerized and stored until samples are analyzed. If the samples indicate that the well water is contaminaed, the site-specific project plan should specify the method of handling or disposal.

65
Q

Gas Pressure displacement system.

A

In a gas pressure displacement system, the water is displaced up the discharge tube by the incresed gas pressure above the water level. It is particularly useful when the well depth is beyond the lifting capacity of a peristatltic pump. However , the portn3etial fo rincreased gas diffusion into the water makes this system unsuitable when sampling for volatile (vapourous) organic compoumds or for most ph factors.

66
Q

Pumps

Submersible Pumps

A

Submersible pumps are portable and have relatively high pumping rates. However, they are heavy, awkward, expensive and difficult to decontaminate in the field. Sometimes a dedicated submersible pump will be left at each well.

67
Q

Peristaltic Pumps

A

they are limited in their lifting capacity; however, they have an advantage in that the same system can be used not only for purging but also for sample collection.

68
Q

Sample collection

A

a peristaltic pump is usefule when relatrively large samples are needed. However, a pump system can strip volatile components as a result of the vacuum created by lifting. Therefore, volatile organic analysis samples should be collected using a bailer.

When collecting a sample with a peristaltic pump, the following guidelins should be followed:

  • install clean medical-grade silicon tubing in the pump head.
  • attache the pump to the required length of teflon sucction line and lower it to the mid-point of the well screen or slightly below the existing water level.
  • the first liter of liquid collected is considered a system purge
  • fill sample bottles, letting the discharge flow gently down the side of the bottle with a minimum of turbulence (disturbance)
  • Preserve the sample (if directed by EPA sampling guidelines) check the Teflon liner in the cap and then secure the cap.
  • Complete the label, the chain-of-custody form, and the log entry.
  • Place the sample bottle in a carrying container at 4 degrees celcius
  • Allow the system to drain, disassemble, and return tubing for decontamination.
69
Q

Bailers

A

Bailers are useful when samples must be taken from depths beyond a pump’s lifting capacity and when volatile component stripping is a concern. A bailer allows samples to be recovered with a minimum of aeration (ie mixing with air). This is accomplished by slowly lowering the bailer until it contacts the water and then, allowing the bailer to sink as it fills. The disadvantage of using bailers is that they are time-consuming because of their limited sample volume. In addition, transfer of the sample to the collection jar can cause aeration. Pouring the water slowly down the side of the sample bottle limits aeration, by avaiding turbulence.

70
Q

Con tainer sample opening

A

Drums are usually opened and sampled in place during site investigations. However, remedial and emergency operations may require a separate drum opening area. Provedures for opening drums are the same, regardless of there the drums are opened.

71
Q

Remote-controlled opening

A

Use the following remote-controlled devices for opening drums:

Pneumatically operated impact wrench to remove bungs

  • Hydraulically or pneumatically operated drum piercers.
  • Backhoes equipped with bronze spikes for penetrating drum tops in large-scale operations.
72
Q

Selection of Sampling Equipment

A

selection of sampling equipment is dependent on the material and contacinre. Scoops, triers, corers, sludge judges or a grain theif can be used for collection.

When testing containerized liquids, the selection of sampling equipment isd dependednt on the material and the container. A device that is commonly used is a drum theif. These glass tubes are inexpensive and can be disposed of instead of decontaminated. One drawback is that if the liquid has a low viscosity it can be difficult to maintain the cavuum in the tube and the sample can dribble from the tube as it is withdrawn from the drum. Also, glass tubing should not be used with materials acontaining hydroflouric acid or strong alkali solutions.