
- •Air sampling and industrial hygiene engineering. Martha j. Boss & Dennis w. Day
- •4.1 Definitions
- •4.2 Example—outline of bulk sampling qa/qc procedure
- •4.3 Example—outline of the niosh 7400 qa procedure
- •4.3.1 Precision: Laboratory Uses a Precision of 0.45
- •4.3.2 Precision: Laboratory Uses a Precision sr that is Better Than 0.45
- •4.3.3 Records to Be Kept in a qa/qc System
- •4.3.4 Field Monitoring Procedures—Air Sample
- •4.3.5 Calibration
- •4.4 Sampling and analytical errors
- •95% Confident That the Employer Is in Compliance
- •95% Confident That the Employer Is not in Compliance
- •4.5 Sampling methods
- •4.5.1 Full-Period, Continuous Single Sampling
- •4.5.2 Full-Period, Consecutive Sampling
- •4.5.3 Grab Sampling
- •4.6 Calculations
- •4.6.1 Calculation Method for a Full-Period, Continuous Single Sample
- •4.6.2 Sample Calculation for a Full-Period, Continuous Single Sample
- •4.6.3 Calculation Method for a Full-Period Consecutive Sampling
- •4.7 Grab sampling
- •4.8 Saes—exposure to chemical mixtures
- •5.1 Baseline risk assessment
- •5.2 Conceptual site model
- •5.2.1 Source Areas
- •5.2.2 Possible Receptors
- •5.3 Chemicals of potential concern
- •5.4 Human health blra criteria
- •5.5 Toxicity assessment
- •5.6 Toxicological profiles
- •5.7 Uncertainties related to toxicity information
- •5.8 Potentially exposed populations
- •5.8.1 Exposure Pathways
- •5.8.2 Sources
- •5.9 Environmental fate and transport of copCs
- •5.10 Exposure points and exposure routes
- •5.11 Complete exposure pathways evaluated
- •5.12 Ecological risk assessment
- •5.13 Data evaluation and data gaps
- •5.14 Uncertainties
- •5.14.1 Uncertainties Related to Toxicity Information
- •5.14.2 Uncertainties in the Exposure Assessment
- •5.15 Risk characterization
- •5.16 Headspace monitoring—volatiles
- •5.18 Industrial monitoring—process safety management
- •5.19 Bulk samples
- •6.1 Fungi, molds, and risk
- •6.1.1 What Is the Difference between Molds, Fungi, and Yeasts?
- •6.1.2 How Would I Become Exposed to Fungi That Would Create a Health Effect?
- •6.1.3 What Types of Molds Are Commonly Found Indoors?
- •6.1.4 Are Mold Counts Helpful?
- •6.1.5 What Can Happen with Mold-Caused Health Disorders?
- •6.2 Biological agents and fungi types
- •6.2.1 Alternaria
- •6.3 Aspergillus
- •6.4 Penicillium
- •6.5 Fungi and disease
- •6.6 Fungi control
- •6.6.1 Ubiquitous Fungi
- •6.6.2 Infection
- •6.6.3 Immediate Worker Protection
- •6.6.4 Decontamination
- •6.6.5 Fungi and voCs
- •6.6.6 Controlling Fungi
- •6.7 Abatement
- •Indoor Air Quality and Environments
- •7.1 Ventilation design guide
- •7.2 Example design conditions guidance
- •7.2.1 Outside Design Conditions
- •7.2.2 Inside Design Conditions
- •7.3 Mechanical room layout requirements
- •7.4 Electrical equipment/panel coordination
- •7.5 General piping requirements
- •7.6 Roof-mounted equipment
- •7.7 Vibration isolation/equipment pads
- •7.8 Instrumentation
- •7.9 Redundancy
- •7.10 Exterior heat distribution system
- •7.10.1 Determination of Existing Heat Distribution Systems
- •7.10.2 Selection of Heat Distribution Systems
- •7.10.2.1 Ag Systems
- •7.10.2.2 Cst Systems
- •7.10.2.3 Buried Conduit (preapproved type)
- •7.10.2.4 Buried Conduit (not preapproved type)
- •7.11 Thermal insulation of mechanical systems
- •7.12 Plumbing system
- •7.12.1 Piping Run
- •7.13 Compressed air system
- •7.13.1 Compressor Selection and Analysis
- •7.13.2 Compressor Capacity
- •7.13.3 Compressor Location and Foundations
- •7.13.4 Makeup Air
- •7.13.5 Compressed Air Outlets
- •7.13.6 Refrigerated Dryer
- •7.14 Air supply and distribution system
- •7.14.1 Basic Design Principles
- •7.14.2 Temperature Settings
- •7.14.3 Air-Conditioning Loads
- •7.14.4 Infiltration
- •7.14.5 Outdoor Air Intakes
- •7.14.6 Filtration
- •7.14.7 Economizer Cycle
- •7.15 Ductwork design
- •7.15.3 Evaporative Cooling
- •7.16 Ventilation and exhaust systems
- •7.16.1 Supply and Exhaust Fans
- •7.17 Testing, adjusting, and balancing of hvac systems
- •7.18 Ventilation adequacy
- •7.19 Laboratory fume hood performance criteria
- •7.20 Flow hoods
- •7.21 Thermoanemometers
- •7.22 Other velometers
4.7 Grab sampling
If a series of grab samples (e.g., detector tubes) is used to determine compliance with either an 8-h TWA limit or a ceiling limit, consult with an industrial hygienist (ARA) regarding sampling strategy and the necessary statistical treatment of the results obtained.
4.8 Saes—exposure to chemical mixtures
Often an employee is simultaneously exposed to a variety of chemical substances in the workplace. Synergistic toxic effects on a target organ are common for such exposures in many construction and manufacturing processes. This type of exposure can also occur when impurities are present in single chemical operations. New PELs for mixtures, such as the recent welding fume standard (5 mg/m3), addresses the complex problem of synergistic exposures and their health effects. In addition 29 CFR 1910.1000 contains a computational approach to assess exposure to a mixture. This calculation should be used when components in the mixture pose a synergistic threat to worker health.
Whether using a single standard or the mixture calculation, the SAE of the individual constituents must be considered before arriving at a final compliance decision. These SAEs can be pooled and weighted to give a control limit for the synergistic mixture. To illustrate this control limit, the following example using the mixture calculation is shown. The mixture calculation is expressed as:
Em = (Q/L, + C2/L2) + . . . Q/LJ where
Em = equivalent exposure for a mixture (Em should be < 1 for compliance)
С = concentration of a particular substance
L = PEL
For example, to calculate exposure to three different, but synergistic substances:
Material 8-h exposure 8-h TWA PEL (ppm) SAE
Substance 1 500 1000 0.089
Substance 2 80 200 0.11
Substance 3 70 200 0.18
Using Equation I: Em = 500/1000 + 80/200 + 70/200 = 1.25
Since Em > 1, an overexposure appears to have occurred; however, the SAE for each substance also needs to be considered:
Exposure ratio (for each substance): Yn = Cn/LK
Ratio to total exposure: Rj = Yj/Eml. . . Rn = Yn/Em
The SAEs (95% confidence) of the substance comprising the mixture can be pooled by:
(RSt2) = [(R*) (SAE^) + (R22) (SAE22) + . . . (Rn2) (SAEn2)]
The mixture control limit (CL) is equivalent to 1 + RSt.
—If Em < CLj, then an overexposure has not been established at the 95% confidence level; further sampling may be necessary. —If Em > 1 and Em > CLj, then an overexposure has occurred (95% confidence).
Using the mixture data above:
= 80/200 |
Y3 = 70/200 |
= 0.4 |
Y3 = 0.35 |
= 0.32 |
R, = 0.28 |
Y, = 500/1000 Y, = 0.5
(RSt)2 = (0.42)(0.0892) + (0.322)(0.112) + (0.282)(0.182)
RSt = [(RSt)2)](l/2) = 0.071
CL = 1 + RSt = 1.071
Em = 1.25
Therefore Em > CL and an overexposure has occurred within 95% confidence limits. This calculation is also used when considering a standard such as the one for total welding fumes.
CHAPTER 5
Chemical Risk Assessment
Real-world examples portray the decision logic needed to conduct chemical sampling when assessing risk. This chapter includes a troubleshooting section/checklist to assist samplers in either choosing a consultant or appraising in-house sampling methodology.
Chemical risk assessment is a twofold process. One part occurs off-site as known chemical information is assessed and calculations based on accepted formulas are done. The EPA baseline risk assessments (BLRAs), screening assessments, and remedial investigation studies rely on a body of knowledge accumulated over the last 20 years. Decisions about supportive air monitoring and actual on-site monitoring required during sampling events should also be made at this time.
The second stage is the actual accumulation of data during which workers must be protected against airborne hazards, including those resulting from their sampling efforts, including disturbance of the on-site medium (soil, water). Decision-making concerning personal protection and engineering controls may require air monitoring of personnel, area of influence, and the site perimeter.
In order to understand the context under which air monitoring protocols are developed, an understanding of chemical risk assessment for these sites is necessary. Keep in mind that the term site is an all inclusive one for this section and may include active industrial and/or construction sites.