Posts Tagged ‘EPA Method TO-15’

Total Volatile Organic Compound (TVOC) Measurement for LEED/Green Building Evaluation

Wednesday, May 27th, 2009

LEED Testing

Background

Total Volatile Organic Compounds (TVOC) may be evaluated when building designers/managers are pursuing the Leadership in Energy and Environmental Design Green Building Rating System for New Construction (LEED-NC) EQ Credit 3.2. The latest LEED-NC guidance document specifies that the maximum allowed concentration of TVOC measured in a building (post construction, pre-occupancy) is 500 µg/m3; the guidance also mentions using the sampling/analytical methods in the US EPA Compendium of Methods for the Determination of Air Pollutants in Indoor Air. However, none of these sampling and analytical methods address TVOC in particular, and thus the existing methods must be modified. In addition, TVOC is not defined (in terms of boiling point range, etc.) in the latest LEED-NC guidance and therefore is left open for interpretation; historically, many definitions of “TVOC” exist in literature.

For TVOC measurement, the analytical technique used must always reference one compound for calibration purposes. All compounds detected are then assumed to have the same response factor as the calibration compound. For instance, handheld instruments are most often calibrated using isobutylene or methane, and laboratory-based methods may reference TVOC as hexane (C6), toluene, or some other chemical species.

In practice, indoor air quality practitioners may use several different techniques for evaluating TVOC in buildings. Each sampling & analytical method has its own benefits and drawbacks, cost implications, and applicability.

(more…)

Update to Massachusetts Air Petroleum Hydrocarbons (APH) Method

Thursday, April 16th, 2009

MassDEP APH MethodThe Massachusetts Department of Environmental Protection (MassDEP) recently updated and finalized their Air-Phase Petroleum Hydrocarbons (APH) analytical method. The APH method, which had been in draft format since February 2000, was completed last year by a MassDEP Workgroup and approved after a month long public comment period in December 2008. The committee was comprised of MassDEP personnel, laboratory experts and data users.

The most significant updates to the APH method include:

  • Analyte List Revisions - 2-Methylnaphthalene was removed from the target analyte list and is no longer considered an air-phase petroleum hydrocarbon. In addition, laboratories will no longer report the “unadjusted” hydrocarbon ranges.
  • Calibration Standards Revisions - Indene, hexylcyclohexane and 1-methynaphthalene were removed as hydrocarbon range calibration standards/retention time markers, due to poor performance and stability in the whole air matrix.
  • Standard Preparation – The newly revised method will only allow vapor phase standards to be used for calibration. (Previously, in the draft method, methanol based standards were allowed.)
  • Calibration & Quality Control Requirements, Holding Time and Performance Standards – Many small changes were made in order to make the APH method consistent with EPA Method TO-15.

The MassDEP APH method is currently the only existing method to look at vapor phase hydrocarbons in a risk based corrective action approach (i.e. with fractionated aliphatic and aromatic ranges). Going beyond EPA Method TO-15 or a traditional total petroleum hydrocarbons (TPH) approach, this method provides more specific information about the type of hydrocarbon contamination at a site.

As an example of the utility of the APH method, Figure 1 shows the total ion chromatogram for a soil gas sample collected at a site impacted by historical subsurface petroleum product contamination. For this example, all the APH target compounds (1,3-butadiene, benzene, toluene, ethylbenzene, xylenes, MTBE, and naphthalene) as well as several other petroleum indicator species (1,2,4-trimethylbenzene, 1,3,5-trimethylbenzene, n-nonane, n-decane, n-dodecane, n-undecane) were not present above the laboratory reporting limit. However, as is visually evident, there was still a strong weathered petroleum pattern present in the sample. The hydrocarbon ranges reported in the APH method were able to capture this information which otherwise might have been overlooked in a basic review of the numerical results.

Total Ion Chromatogram of Real-World APH Sample

Figure 1. - Total Ion Chromatogram of Real-World APH Sample

- - -

References (Current as of December 2008)

1. MassDEP Method for the Determination of Air-Phase Petroleum Hydrocarbons (APH), December 2008. Available at: http://www.mass.gov/dep/cleanup/laws/qaqcdocs.htm#IV

2. MassDEP Standard Operating Procedure for Indoor Air Contamination, SOP-BWSC-07-01, August 2007 (made available April 2008). Available at: http://www.mass.gov/dep/cleanup/laws/policies.htm#iasop

3. MassDEP Indoor Air Sampling & Evaluation Guide, WSC Policy #02-430, April 2002. Available at: http://www.mass.gov/dep/cleanup/laws/policies.htm#indair

- - -

View the APH method flyer (PDF file)

Read about testing for petroleum hydrocarbon contaminations

- - -

Analytical Considerations for Air Samples for Vapor Intrusion Investigations

Monday, February 5th, 2007

The term “vapor intrusion” refers to the migration of volatile chemicals from subsurface contaminated sources into overlying residential or commercial structures. “Historically, it was thought that vapor intrusion was only an issue where the source of the contaminants was very shallow and the magnitude of the contamination was very great. It is now known that the previous assumptions about the mechanisms that could lead to exposure to vapor intrusion were not complete (NYS DEC DER Vapor Intrusion Guidance).” For a growing number of federal, state and local agencies, as well as environmental consultants and laboratories, vapor intrusion could emerge as the next major environmental challenge.

Vapor intrusion is not a new phenomenon— for some environmental experts, it has been recognized as a potential pathway of contamination for almost 20 years. In the late 1980s, the first vapor intrusion studies were carried out to evaluate potential health effects from chronic exposure to volatile organic compounds. Presently, vapor intrusion is of growing concern to the environmental community due to a number of factors, such as increased recognition of it as a potential pathway for exposure and the risks associated with that exposure, as well as the location and the number of potential sites for investigation and remediation. With this increased focus comes ongoing debate regarding the mechanism of the exposure pathway, compliance concentrations of contaminants, identification of sites, sampling approaches, analytical methodology, use and validity of current models, screening approaches, and risk assessment, among other topics.

What this has meant for many laboratories specializing in air analyses is an upward trend in the number of ambient air, indoor air, soil gas and sub-slab samples submitted each year for volatile organic compound (VOC) analyses. The primary compounds of concern are often chlorinated VOCs. Trichloroethene (TCE) and tetrachloroethene (PCE), in particular, are common targets of the investigations due to the health risks associated with these compounds and their breakdown products.

In instances where the project specific objectives of the vapor intrusion investigation call for sampling, several kinds of air samples can be collected: soil vapor, ambient (outdoor) air, indoor air and sub-slab vapor. The timing of the collection, as well as the number, placement and combination of samples will all vary depending on the client-defined sampling protocol, which ultimately relies on local, state or federal requirements.

So, keeping in mind the client’s project-specific objectives and the underlying regulatory requirements, here are some of the factors to be taken into consideration for the analytical portion of a vapor intrusion investigation:

Analytical Method

EPA Method TO-15 is the most frequently requested method for the analysis of VOCs for the range of air samples associated with vapor intrusion investigations. The method uses gas chromatography (GC) to achieve sample separation and a mass spectrometer (MS) for identification and quantitation.

TO-15 was a new method added to the Second Edition of the Compendium of Methods for the Determination of Toxic Organic Compounds in Ambient Air in January 1999. Although very similar to EPA Method TO-14A, EPA Method TO-15 is larger in scope and better defined for the analysis of VOCs in air and other gaseous matrices than TO-14A (which is a revised and updated version of the former Method TO-14).

Compound List

A wide range of compounds may be analyzed by EPA TO-15 including alkanes, alkenes, aromatics, halogenated VOCs, ketones, esters and some alcohols. Some aldehydes and sulfides may also be evaluated using this method.

EPA TO-15 does not specify a target compound list in the method. As a result, there is some variation among commercial environmental laboratories in the compound lists that are available for VOCs. Target compound lists may include anywhere from 40 to 60 compounds or more, and may provide results in μg/m3, ppbV, or both.

Compound lists can usually be tailored to meet project-specific objectives. This is true especially in the case of indoor air, which typically involves a subset of the laboratory’s standard target compound list.

Method Reporting Limits

Target method reporting limits (MRLs) will vary depending on the data quality objectives of the investigation, which should take into account any state or federal regulatory documents or guidances that may apply.

For soil gas or sub-slab samples, it is usually sufficient to analyze the samples in the normal operating mode of the GC/MS (SCAN), which yields MRLs from sub-parts per billion up to parts per million levels.

For indoor or ambient air analyses, investigators are often considering the potential risk to human health, so they are typically interested in lower MRLs, down to the single digit part per trillion levels. Indoor air and ambient air analyses are frequently performed by GC/MS in Selective Ion Monitoring (SIM) mode to achieve these ultra-low level MRLs.

The risk-based levels for the contaminants of concern are, in many cases, less than the typical or observed background levels in the indoor or outdoor environment, creating a challenge for many vapor intrusion investigations. The best approach for assessing and dealing with this issue continues to be discussed and debated by experts in the field.

Sampling Media

For soil gas determinations, samples may be collected using either passivated stainless steel canisters (such as Summa canisters) or Tedlar bags. Each sampling medium has its advantages and disadvantages, as summarized in the table below.

For soil gas sampling, 1L Summa canisters can offer certain benefits over the larger 6L canisters. They fill faster, reducing time in the field for the investigators. They are smaller and lighter, so they are easier to transport, handle and ship. The smaller volume reduces the likelihood of ambient air intrusion, especially when sampling more densely packed soils. The trade off is that a smaller sample portion can be withdrawn from the canister for the analysis, which results in higher MRLs than those achievable from samples collected in a larger canister, typically 3 to 5 times higher.

For indoor air or ambient air sampling, 6L Summa canisters are the recommended sampling medium. Canisters may be either batch certified clean or individually certified clean—the selection depends, again, on the data quality objectives of the project and on any regulatory specifications. In situations where it may be valuable to have documentation for every canister, (e.g. potential litigation, risk assessment), then individual certification can be requested. In either case, the canisters will be cleaned and certified below the target MRLs.

Columbia Analytical’s Air Quality Laboratory has extensive experience performing analyses of indoor and ambient air, as well as sub-slab and soil gas samples. Specializing in the analysis of volatile and semi-volatile organic compounds, sulfur compounds and other hazardous substances in a wide variety of air and vapor matrices since 1988, the lab has performed tens of thousands of analyses from its southern California location near Los Angeles, and it successfully serves clients in all 50 states and around the globe.