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Dioxin equivalents, measuring toxicity

Concern has been expressed about the possible formation of dioxins and furans. However, measurements during experiments indicated that the emissions of dioxins and furans were not significantly elevated. Dioxin emissions with or without plastic input appeared to be about a factor of 100 below the standard of 0.1 ng/Nm TEQ TCCD (toxicity equivalent in relation to the toxic dioxin TCCD) (a.7). This might be due to the benefit of the strongly reducing atmosphere and the high temperature of 2100 °C. In total, until now the conclusion has been that at current PVC levels in MSW, pretreatment for chlorine removal is unnecessary. [Pg.9]

Ah-receptor-mediated toxicity is particularly associated with the highly toxic compound 2,3,7,8-tetrachloro-dibenzo-p-dioxin (TCDD), commonly referred to as dioxin. TCDD, and the concept of toxicity equivalency factors (TEFs) based on TCDDs, will be dealt with in Chapter 7. The main point to make at this juncture is that the toxicity of each individual coplanar congener in a mixture can be expressed in terms of a toxic equivalent calculated relative to the toxicity of dioxin. Summation of the toxic equivalents of the individual coplanar PCBs gives a measure of the toxicity of the whole mixture, as expressed through the Ah receptor mechanism. [Pg.144]

Toxic equivalency factors (TEFs) are estimated relative to 2,3,7,8-TCDD, which is assigned a value of 1. They are measures of the toxicity of individual compounds relative to that of 2,3,7,8-TCDD. A variety of toxic indices, measured in vivo or in vitro, have been used to estimate TEFs, including reproductive effects (e.g., embryo toxicity in birds), immunotoxicity, and effects on organ weights. The degree of induction of P450 lAl is another measure from which estimations of TEF values have been made. The usual approach is to compare a dose-response curve for a test compound with that of the reference compound, 2,3,7,8-TCDD, and thereby establish the concentrations (or doses) that are required to elicit a standard response. The ratio of concentration of 2,3,7,8-TCDD to concentration of test chemical when both compounds produce the same degree of response is the TEF. Once determined, a TEF can be used to convert a concentration of a dioxin-like chemical found in an environmental sample to a toxic equivalent (TEQ). [Pg.155]

PCDDs and PCDEs, together with coplanar PCBs, can express Ah-receptor-mediated toxicity. TCDD (dioxin) is used as a reference compound in the determination of TEFs, which can be used to estimate TEQs (toxic equivalents) for residues of PHAHs found in wildlife samples. Biomarker assays for Ah-receptor-mediated toxicity have been based on the induction of P450 lAl. TEQs measured in field samples have sometimes been related to toxic effects upon individuals and associated ecological effects (e.g., reproductive success). [Pg.160]

To control the emission of organics, these units must comply with similar DRE requirements to the other hazardous waste combustion units. Owners or operators of MACT combustion units must select POHCs and demonstrate a DRE of 99.99% for each POHC in the hazardous wastestream. Sources that bum hazardous waste have a required DRE of 99.9999% for each POHC designated. Additionally, for dioxins and furans, U.S. EPA promulgated more stringent standards under MACT. For example, MACT incinerators and cement kilns that bum waste with dioxins and furans must not exceed an emission limitation of either 0.2 ng of toxicity equivalence per dry standard cubic meter (TEQ/m3) or 0.4 ng TEQ/m3 at the inlet to the dry particulate matter control device. This unit of measure is based on a method for assessing risks associated with exposures to dioxins and furans. [Pg.463]

Commercial PCB mixtures frequently contain impurities that may contribute to the 2,3,7,8-TCDD toxic equivalency factor. These impurities may include other PCBs, dioxins, dibenzofurans, naphthalenes, diphenyl ethers and toluenes, phenoxy and biphenyl anisoles, xanthenes, xanthones, anthracenes, and fluorenes (Jones etal. 1993). PCB concentrations in avian tissues sometimes correlate positively with DDE concentrations (Mora et al. 1993). Eggs of peregrine falcons (Falco peregrinus) from California, for example, contained measurable quantities of various organochlorine compounds, including dioxins, dibenzofurans, mirex, hexachlorobenzene, and / ,//-DDE at 7.1 to 26.0 mg/kg FW PCB 126 accounted for 83% of the 2,3,7,8-TCDD equivalents, but its interaction with other detectable organochlorine compounds is largely unknown (Jarman et al. 1993). [Pg.1286]

Schecter, A. J., Piskac, A. L. (2001) PCBs, dioxins, and dibenzofiuans measured levels and toxic equivalents in blood, milk and food from various countries. PCBs Recent Advances in Environmental Toxicology and Health Effects, 2001 161-168. [Pg.268]

Usually in the context of environmental remediation, human potential hazard, or/and comparison of dioxin-like compounds, DLC, an estimation of the toxic potency of the whole sample is desired, rather than the concentrations of the sample s components. One such measure, the toxic equivalents, TEQ, is obtained from the analytical data by using Toxic Equivalency Factors, TEFs, relating the potency of DLC X to the potency of TCDD, taken as a reference toxicant (TEF = 1). In this TEF scheme, the toxicity of any PCDD or PCDF congener is related, using animal data, to the amount ofTCDD that would have equal toxicity (Table 3). [Pg.375]

Advantages of the Process. The formation of dioxins is prevented by the high oxidation temperature (1200 °C), the residence time of 2 s in the reactor, the mainly homogeneous temperature profile in the oxidation chamber, and the quench cooling of the reaction gases from 1200 to 85 °C. Measured concentrations are <0.1ng/m toxicity equivalents dioxins and furans. [Pg.44]

Sum of measured dioxin and furan congener concentrations converted to the toxic equivalent concentration of 2,3,7,8-tetrachlorodibenzodioxin (T4CDD). [Pg.5]


See other pages where Dioxin equivalents, measuring toxicity is mentioned: [Pg.146]    [Pg.244]    [Pg.409]    [Pg.84]    [Pg.168]    [Pg.1029]    [Pg.24]    [Pg.39]    [Pg.1029]    [Pg.37]    [Pg.9]    [Pg.268]    [Pg.276]    [Pg.311]    [Pg.935]    [Pg.206]    [Pg.94]    [Pg.46]    [Pg.233]    [Pg.631]    [Pg.498]    [Pg.625]    [Pg.125]    [Pg.496]    [Pg.32]   


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