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Measurement and Analysis
To identify and quantify chemical health

    hazards
    Health effects can be acute or chronic, so there

    are different types of measurement to account
    for this:
      Long-term measurements to assess average
    
      exposure over a given time period
     Continuous measurements that can detect short-
      term acute exposure to high concentrations of
      contaminants
     Spot readings to measure acute exposure if the exact
      point in time exposure is known
2 types of sampling:

        Static sampling
    
         Primary aim is to assess effectiveness of engineering
          controls or measure plant emissions into work
          environment
         Levels should be set well below personal exposure
          limits
        Personal sampling
    
         Assess individual exposure
Factors influencing airborne concentrations:

      No. of sources of contaminant
    
     Rates of release from each source
     Type and position of each source
     Dispersion or mixing of contaminants
     Ambient conditions e.g. wind speed, air temp.
Before devising sampling strategy, carry out

    initial appraisal. Info. required:
      Substances which occur in workplace
    
     Airborne nature of substances
     Hazardous properties of substances
     Synergistic effects
     Possible exposure by inhalation, ingestion, skin
      contact?
     During which processes/tasks will exposure occur?
     Groups/individuals at risk
     Likely pattern and duration of exposure
Initial Appraisal:

        Simple qualitative tests can be carried out:
    
         Dust lamps
         Smoke tubes
         Stain tubes
Strategies:

      First level for basic surveys
    
     Second level for more detailed surveys
     Third Level for surveys needing high degree of
      sophistication
First level strategies:

      Used where crude quantitative information is
    
      required so that decisions can be taken as to whether
      problem actually exists, prior to conducting detailed
      survey
     Divide population into groups in relation to work or
      degree of exposure
     High risk groups can be studied in detail
     Personal sampling, especially at peak periods
Second level strategies:

      Appropriate for most detailed surveys and for
    
      routine monitoring
     Emphasis on accurate measurement of average
      exposures and relating them to OEL’s
     Entire period of exposure should be covered
Third level strategies:

        Occasionally high degree of sophistication required
    
        E.g. if all reasonably practicable steps have been
    
        taken and exposure is still close to OEL; or
        Where OEL is very low so small changes in exposure
    
        are significant
Consideration of results should always lead to

    answers to 5 questions:
        Is immediate action necessary to eliminate or reduce
    
        exposure?
        Is immediate action necessary to re-establish
    
        adequate control?
        Is a programme of planned improvements
    
        necessary?
        Is a more detailed survey required?
    
        Should routine monitoring be implemented or
    
        continued?
Series of detailed descriptions of analytical

    methods approved by HSE
    Provide reliable and consistent methods


    Covers sampling AND analysis

2 Fractions:

        Inhalable fraction:
    
         Total particles inhaled through nose and mouth
        Respirable fraction
    
         Less than 10 microns
         Able to penetrate the respiratory system as far as the
          alveolar region
    Fibrous particles:

        Shape is as important as size
    
        Long thin fibres more dangerous
    
Components:

        Sampling head
    
        Size selection
    
         Cyclones to separate respirable fraction
        Filters
    
         Used to collect sample before assessment
         Wide range depending on contaminant
        Pumps
    
         Must be able to be worn on body if personal sampling
          required
         Flow meter required
Static sampling:

        Complete assembly includes filter, pump and flow
    
        meter
        Left unattended in workplace
    
        Use cyclones to remove larger particles
    

    Personal sampling:

      Preferred technique - more realistic measurement of
    
      exposure
     Cyclones used to remove larger particles
Direct Reading Instruments:

        Gives instantaneous result
    
        Can be:
    
         Light scattering
         Beta particle attenuation
         Oscillating micro-balance (quartz crystal oscillation
         changes with build up of dust)
Measured volume of air drawn through filter


    Mass of dust collected is determined by weighing filter

    before and after sampling
    Size selection devices can be used to measure respirable

    dust
    Volume of air passing through filter is calculated by

    multiplying flow rate (cubic m per minute) by
    sampling time (minutes)
    Weight gain of filter (mg), divided by the volume

    sampled, gives average dust concentration in mg per
    cubic meter of air (mg/m3)
Similar to dust, except:

      Open faced filter holder
    
     Membrane filters which can be rendered transparent
      to allow fibre counting by phase contrast microscopy
     Flow rate is specified and measurement must be over
      4 hour period
     Fibres are counted on membrane filter
     Concentration is calculated by dividing total no. of
      fibres collected on filter by total volume of air to give
      fibres per millilitre (f/ml)
Grab Sampling:

        Sample taken in flask, bottle bag etc.
    
        Useful for peak concentration or when
    
        concentrations are constant
    Continuous or Long-Term Sampling:

        Sample removed from air over measured time
    
        period and concentrated by passage through solid or
        liquid sorbent
        Useful if:
    
         Concentration varies time with time
         Concentration is low
         TWA exposure is required
Evacuated flasks

        Atmosphere drawn in
    

    Gas/Liquid displacement container

        Flask connected to a pump
    

    Flexible plastic containers

        Plastic bags
    

    Hypodermic syringes

Liquid sorbents


    Cold traps


    Plastic sampling bags


    Solid sorbents

        Charcoal or Silica gel
    
Sampling equipment:

        Pump
    
         Adjustable flow rate
         Able to be worn if personal sampling required
        Flow measurement
    
         Important to know flow rate to calculate exposure
Diffusive samplers

        Badge or tube type
    
        Factors affecting performance:
    
         Temperature and pressure
         Humidity
         Concentration variations
         Sorbent efficiency
         Face velocity
Sample positioning:

      General working atmosphere (grab sample)
    
     Operator’s breathing zone (TWA sample)
     Close to contaminant generation (continuous
      monitored sample)
    Sampling frequency:

        Statutory in some cases (asbestos every 4 hours)
    
        Depends on level of risk
    
Most involved subjecting substance to burst of energy and

    examining way substance responds
    Response is characteristic of substance and can be used as

    “fingerprint”
    Magnitude of response can be used to estimate how much of

    agent is present
    Techniques:

        Gas Chromatography
    
        Atomic Absorption Spectroscopy
    
        Infra Red Spectroscopy
    
        X-Ray Diffraction
    
        Optical Microscopy
    
Chemical is carried down an absorbent column

    by a carrier gas
    The length of time the sample takes to travel

    down the column is unique to the substance
    Size of spectrum peak indicates quantity of

    substance
    Mixed substance can be separated

Used for metallic substances


    If certain metals are heated to high temperatures

    in a flame, electronic changes in the metal atom
    cause a change in colour to the flame
    Sample is injected into an air-acetylene flame

    and resultant spectrum is analysed by an atomic
    absorption spectrometer
    Both identity and quantity of substance can be

    determined
Based on principle that chemical bonds that

    connect atoms into molecules are continuously
    vibrating and the energy of this vibration falls
    within the infra-red wavelength range
    Infra-red radiation is passed through the

    sample and the absorption spectrum gives a
    characteristic fingerprint of the substance
    Identifies and quantifies substance

Used for solid analysis


    X-rays passed through a sample are diffracted

    in a characteristic fashion, which depends on
    the crystal structure and spacing between
    atoms
    Gives characteristic fingerprint of substance

Mostly widely used for fibrous dust


    Dust is collected on membrane filter, then

    counted under optical microscope
    As sampling time and flow rate are know,

    fibres per unit volume can be calculated
    Where it is necessary to determine type of

    asbestos, polarised light microscopy is used
    Different types of fibre show different colours

    under polarised light

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Measurement and Analysis of Chemical Health Hazards

  • 2. To identify and quantify chemical health  hazards Health effects can be acute or chronic, so there  are different types of measurement to account for this: Long-term measurements to assess average  exposure over a given time period  Continuous measurements that can detect short- term acute exposure to high concentrations of contaminants  Spot readings to measure acute exposure if the exact point in time exposure is known
  • 3. 2 types of sampling:  Static sampling   Primary aim is to assess effectiveness of engineering controls or measure plant emissions into work environment  Levels should be set well below personal exposure limits Personal sampling   Assess individual exposure
  • 4. Factors influencing airborne concentrations:  No. of sources of contaminant   Rates of release from each source  Type and position of each source  Dispersion or mixing of contaminants  Ambient conditions e.g. wind speed, air temp.
  • 5. Before devising sampling strategy, carry out  initial appraisal. Info. required: Substances which occur in workplace   Airborne nature of substances  Hazardous properties of substances  Synergistic effects  Possible exposure by inhalation, ingestion, skin contact?  During which processes/tasks will exposure occur?  Groups/individuals at risk  Likely pattern and duration of exposure
  • 6. Initial Appraisal:  Simple qualitative tests can be carried out:   Dust lamps  Smoke tubes  Stain tubes
  • 7. Strategies:  First level for basic surveys   Second level for more detailed surveys  Third Level for surveys needing high degree of sophistication
  • 8. First level strategies:  Used where crude quantitative information is  required so that decisions can be taken as to whether problem actually exists, prior to conducting detailed survey  Divide population into groups in relation to work or degree of exposure  High risk groups can be studied in detail  Personal sampling, especially at peak periods
  • 9. Second level strategies:  Appropriate for most detailed surveys and for  routine monitoring  Emphasis on accurate measurement of average exposures and relating them to OEL’s  Entire period of exposure should be covered
  • 10. Third level strategies:  Occasionally high degree of sophistication required  E.g. if all reasonably practicable steps have been  taken and exposure is still close to OEL; or Where OEL is very low so small changes in exposure  are significant
  • 11. Consideration of results should always lead to  answers to 5 questions: Is immediate action necessary to eliminate or reduce  exposure? Is immediate action necessary to re-establish  adequate control? Is a programme of planned improvements  necessary? Is a more detailed survey required?  Should routine monitoring be implemented or  continued?
  • 12. Series of detailed descriptions of analytical  methods approved by HSE Provide reliable and consistent methods  Covers sampling AND analysis 
  • 13. 2 Fractions:  Inhalable fraction:   Total particles inhaled through nose and mouth Respirable fraction   Less than 10 microns  Able to penetrate the respiratory system as far as the alveolar region Fibrous particles:  Shape is as important as size  Long thin fibres more dangerous 
  • 14. Components:  Sampling head  Size selection   Cyclones to separate respirable fraction Filters   Used to collect sample before assessment  Wide range depending on contaminant Pumps   Must be able to be worn on body if personal sampling required  Flow meter required
  • 15. Static sampling:  Complete assembly includes filter, pump and flow  meter Left unattended in workplace  Use cyclones to remove larger particles  Personal sampling:  Preferred technique - more realistic measurement of  exposure  Cyclones used to remove larger particles
  • 16. Direct Reading Instruments:  Gives instantaneous result  Can be:   Light scattering  Beta particle attenuation  Oscillating micro-balance (quartz crystal oscillation changes with build up of dust)
  • 17. Measured volume of air drawn through filter  Mass of dust collected is determined by weighing filter  before and after sampling Size selection devices can be used to measure respirable  dust Volume of air passing through filter is calculated by  multiplying flow rate (cubic m per minute) by sampling time (minutes) Weight gain of filter (mg), divided by the volume  sampled, gives average dust concentration in mg per cubic meter of air (mg/m3)
  • 18. Similar to dust, except:  Open faced filter holder   Membrane filters which can be rendered transparent to allow fibre counting by phase contrast microscopy  Flow rate is specified and measurement must be over 4 hour period  Fibres are counted on membrane filter  Concentration is calculated by dividing total no. of fibres collected on filter by total volume of air to give fibres per millilitre (f/ml)
  • 19. Grab Sampling:  Sample taken in flask, bottle bag etc.  Useful for peak concentration or when  concentrations are constant Continuous or Long-Term Sampling:  Sample removed from air over measured time  period and concentrated by passage through solid or liquid sorbent Useful if:   Concentration varies time with time  Concentration is low  TWA exposure is required
  • 20. Evacuated flasks  Atmosphere drawn in  Gas/Liquid displacement container  Flask connected to a pump  Flexible plastic containers  Plastic bags  Hypodermic syringes 
  • 21. Liquid sorbents  Cold traps  Plastic sampling bags  Solid sorbents  Charcoal or Silica gel 
  • 22. Sampling equipment:  Pump   Adjustable flow rate  Able to be worn if personal sampling required Flow measurement   Important to know flow rate to calculate exposure
  • 23. Diffusive samplers  Badge or tube type  Factors affecting performance:   Temperature and pressure  Humidity  Concentration variations  Sorbent efficiency  Face velocity
  • 24. Sample positioning:  General working atmosphere (grab sample)   Operator’s breathing zone (TWA sample)  Close to contaminant generation (continuous monitored sample) Sampling frequency:  Statutory in some cases (asbestos every 4 hours)  Depends on level of risk 
  • 25. Most involved subjecting substance to burst of energy and  examining way substance responds Response is characteristic of substance and can be used as  “fingerprint” Magnitude of response can be used to estimate how much of  agent is present Techniques:  Gas Chromatography  Atomic Absorption Spectroscopy  Infra Red Spectroscopy  X-Ray Diffraction  Optical Microscopy 
  • 26. Chemical is carried down an absorbent column  by a carrier gas The length of time the sample takes to travel  down the column is unique to the substance Size of spectrum peak indicates quantity of  substance Mixed substance can be separated 
  • 27. Used for metallic substances  If certain metals are heated to high temperatures  in a flame, electronic changes in the metal atom cause a change in colour to the flame Sample is injected into an air-acetylene flame  and resultant spectrum is analysed by an atomic absorption spectrometer Both identity and quantity of substance can be  determined
  • 28. Based on principle that chemical bonds that  connect atoms into molecules are continuously vibrating and the energy of this vibration falls within the infra-red wavelength range Infra-red radiation is passed through the  sample and the absorption spectrum gives a characteristic fingerprint of the substance Identifies and quantifies substance 
  • 29. Used for solid analysis  X-rays passed through a sample are diffracted  in a characteristic fashion, which depends on the crystal structure and spacing between atoms Gives characteristic fingerprint of substance 
  • 30. Mostly widely used for fibrous dust  Dust is collected on membrane filter, then  counted under optical microscope As sampling time and flow rate are know,  fibres per unit volume can be calculated Where it is necessary to determine type of  asbestos, polarised light microscopy is used Different types of fibre show different colours  under polarised light