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TITLE 30ENVIRONMENTAL QUALITY
PART 1TEXAS COMMISSION ON ENVIRONMENTAL QUALITY
CHAPTER 350TEXAS RISK REDUCTION PROGRAM
SUBCHAPTER DDEVELOPMENT OF PROTECTIVE CONCENTRATION LEVELS
RULE §350.76Approaches for Specific Chemicals of Concern to Determine Human Health Protective Concentration Levels

  (1) In demonstrating attainment of the critical PCL for TCDD, 2,3,7,8-(dioxin), the person shall apply the toxicity equivalency factor as shown in the figure in subsection (d)(2)(B) of this section to the measured concentrations in accordance with the following procedures.

    (A) When analytical data are only available for total dioxins/furans, the person shall assume that the mixture consists solely of 2,3,7,8-TCDD, and a toxicity equivalency factor value of 1.0 shall be applied to the measured concentration to yield the 2,3,7,8-TCDD toxicity equivalency quotient concentration for the sample.

    (B) When homologue-specific analytical data are available (e.g., tetrachlorodibenzodioxins), the person shall assume that each homologue class is comprised solely of 2,3,7,8-substituted congeners, and the toxicity equivalency factor specified for the 2, 3, 7, 8-substituted congeners in the homologue class shall be applied to the measured concentrations for that homologue class. A toxicity equivalency factor value of 0.5 should be used for the pentachlorodibenzofuran homologue class. The toxicity equivalency quotient concentrations for each homologue class shall be summed to obtain a total toxicity equivalency quotient concentration for the sample.

    (C) When congener-specific analytical data are available (e.g., 1, 2, 3, 4, 7, 8-hexachlorodibenzofuran), the person shall apply the toxicity equivalency factor for the 2, 3, 7, 8-substituted congeners to the measured concentrations. The toxicity equivalency quotient concentrations for each 2, 3, 7, 8-substituted congener shall then be summed to obtain a total toxicity equivalency quotient concentration for the sample.

  (2) The person shall then compare the total toxicity equivalency quotient concentration established in paragraph (1) of this subsection to the critical PCL for TCDD, 2, 3, 7, 8-(dioxins).

  (3) The critical soil PCL for residential properties for all three tiers is 1 part per billion (ppb) and for commercial/industrial properties for all three tiers is 5 ppb.

(f) Polycyclic Aromatic Hydrocarbons.

  (1) In calculating residential and commercial/industrial PCLs for all tiers, the person shall evaluate the following seven polycyclic aromatic hydrocarbons as carcinogens:

    (A) benzo {a} anthracene;

    (B) benzo {b} fluoranthene;

    (C) benzo {k} fluoranthene;

    (D) benzo {a} pyrene (B {a} P);

    (E) chrysene;

    (F) dibenzo {a, h} anthracene; and

    (G) indeno {1, 2, 3-c, d} pyrene.

  (2) The person shall use the relative potency factors outlined in the following figure to estimate cancer slope factors and unit risk estimates for each of the polycyclic aromatic hydrocarbons identified in paragraph (1) of this subsection for all exposure pathways (e.g., the soil ingestion, vegetable ingestion, inhalation, dermal contact with soil, and groundwater ingestion (in the absence of a primary MCL) exposure pathways):

Attached Graphic

  (3) The cancer slope factors and inhalation unit risk factors for the seven carcinogenic polycyclic aromatic hydrocarbons, shall be calculated according to the equations set forth in the following figure:

Attached Graphic

  (4) The person shall not apply the relative potency factor for any pathways when evaluating noncarcinogenic endpoints.

  (5) For class 1 or 2 groundwater, the person shall establish PCLs according to the procedures in subparagraphs (A) and (B) of this paragraph.

    (A) In evaluating residential and commercial/industrial exposures to class 1 and 2 groundwater for all tiers, the person shall use the most currently available primary MCL for benzo{a}pyrene as GW GWIng for benzo{a}pyrene.

    (B) In establishing GW GWIng for class 1 and 2 groundwater for the six remaining carcinogenic polycyclic aromatic hydrocarbons, the person shall use the higher of the calculated GW RBEL Ing or the primary MCL for B{a}P as GW GWIng for that specific polycyclic aromatic hydrocarbon. In the event that primary MCLs for the other carcinogenic polycyclic aromatic hydrocarbons become available, those MCLs would serve as GW GWIng for these compounds.

(g) Total Petroleum Hydrocarbons.

  (1) The person shall follow the methodology prescribed by this subsection to establish PCLs for total petroleum hydrocarbons, unless the executive director approves the use of an alternate method.

  (2) In order to establish PCLs for total petroleum hydrocarbons, the person shall establish PCLs for each of the aliphatic and aromatic hydrocarbon fractions listed in the following figure (e.g., aliphatic >C 6 -C8 ) for the mandatory and complete or reasonably anticipated to be completed exposure pathways as required in §350.71(c) of this title (relating to General Requirements):

Attached Graphic

  (3) The person shall use the specific toxicity factors for the specific surrogates as shown in the figure in paragraph (2) of this subsection for a hydrocarbon fraction. If a reference concentration is not available, then the person shall not be required to comply with §350.73(c) of this title (relating to Determination and Use of Human Toxicity Factors and Chemical Properties). The PCLs established under this subsection shall be based on noncarcinogenic effects.

  (4) The person shall ensure that the PCLs established for each hydrocarbon fraction comply with the hazard quotient criteria as set forth in §350.72 of this title (relating to Carcinogenic Risk Levels and Hazard Indices for Human Health Exposure Pathways).

  (5) The person shall ensure that the PCLs established for the total petroleum hydrocarbons comply with the hazard index criteria as set forth in §350.72 of this title considering only the hydrocarbon fractions as shown in the figure in paragraph (2) of this subsection. The person shall follow the methodology prescribed in §350.72(d) of this title to adjust the hydrocarbon fraction PCLs to meet the hazard index criteria for the total petroleum hydrocarbons.

  (6) The person shall use an analytical method approved by the executive director to determine the concentration of the hydrocarbon fractions at the affected property.

  (7) When the bulk total petroleum hydrocarbons composition can be assumed to be relatively consistent based on process knowledge, the person may establish mixture-specific (e.g., gasoline, diesel, transformer mineral oil, or other petroleum product) PCLs based on property-specific mixture compositions or mixture compositions considered to be representative of the mixture. The person shall comply with the other provisions of this subsection in the development of the mixture-specific PCLs, but the person shall be allowed to determine compliance with the mixture-specific total petroleum hydrocarbons PCL with a bulk total petroleum hydrocarbons analytical method acceptable to the executive director in lieu of analysis of the concentration of each hydrocarbon fraction.

  (8) The PCLs established for each individual aliphatic and aromatic hydrocarbon fraction used to establish the mixture specific PCLs shall not exceed a hazard quotient of 1 and the mixture-specific PCL shall not exceed a hazard index of 10.


Source Note: The provisions of this §350.76 adopted to be effective September 23, 1999, 24 TexReg 7436; amended to be effective March 19, 2007, 32 TexReg 1526

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