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2,3,7,8-TCDD

The ubiquitous environmental contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) accumulates in animal fat and plant tissues. The food [Pg.146]


Dioxin and Furan Emissions. The emissions of polychlorinated dibenzo-/)-dioxins (PCDD) and polychlorinated dibenzo-furans (PCDF) from incinerators (4) are of interest to the pubHc, scientists, and engineers. The U.S. EPA classifies 2,3,7,8-tetrachlorodibenzo-/)-dioxin (2,3,7,8-TCDD) as the most potent carcinogenic compound it has evaluated. It is also Hsted as the agency s most potent reproductive toxin (4). [Pg.53]

Some hquid defoamers are preemulsified relatives of paste defoamers. In addition to the fatty components mentioned above, kerosene [8008-20-6] or an organic cosolvent such as 2-propanol have been used to enhance stabiUty of the oil—water emulsion and the solubiUty of the defoamer s active ingredients. These cosolvents are used less frequently as concerns increase about volatile organic emissions (VOCs) from the paper machine. Additionally, the use of ultrapure mineral oil in defoamers has become commonplace. Concern about the creation of 2,3,7,8-tetrachlorodibenzodioxin (TCDD) and 2,3,7,8-tetrachlorodibenzofuran (TCDF) in the pulping process has led to the discovery of unchlorinated precursor molecules, especially in recycled mineral oil and other organic cosolvents used in defoamer formulations (28). In 1995 the mineral oil that is used is essentially free of dibenzodioxin and dibenzofuran. In addition, owing to both the concern about these oils and the fluctuating cost of raw materials, the trend in paper machine defoamers is toward water-based defoamers (29). [Pg.16]

In the United States, the Clean Air Act of 1990 requires plants to reduce emissions of 189 toxic and carcinogenic substances such as chlorine, chloroform, and 2,3,7,8-TCDD (dioxin) by 90% over the 1990s. The U.S. Environmental Protection Agency is working to develop standards based on maximum achievable control technologies and the industry has invested bUHons of doUars in capital investments to retrofit or rebuUd plant equipment to meet these measures. [Pg.283]

More subtle modes of action are also possible since the response to hormone receptor binding is complex and could be affected by chemical interference with receptor-related proteins, DNA methylation or histone acetylation. Dioxin (TCDD), for example, reduces the ability of the oestrogen-receptor complex to bind to the oestrogen response element of DNA, reducing gene transcription. ... [Pg.12]

The responsiveness of a tissue to a hormone depends on the density of receptors within its component cells. The number of receptors is determined by their rate of synthesis and catabolism, which is itself controlled by complex feedback mechanisms involving hormone action. Some chemicals are known to interfere with this regulation. For example, TCDD can act to increase or decrease the expression of the oestrogen receptor. ... [Pg.13]

Poteney of eompound relative to 17/ -estradiol (oestrogenieity) or TCDD (anti-oestrogenieity) determined from eell eulture assays. [Pg.20]

Daily exposure in dose equivalents, using 17/ -estradiol aetivity for oestrogenieity (EQ) and TCDD for anti-oestrogenie aetivity (TEQ). [Pg.20]

When the steam was shut off and, 15 minutes later, the agitator was switched off, heat transferred from the hot wall above the liquid level to the top part of the liquid, which became hot enough for a runaway reaction to start. This resulted in a release of TCDD (dioxin), which killed a number of nearby animals, caused dermatitis (chloracne) in about 250 people, damaged vegetation near the site, and required the evacuation of about 600 people (Kletz 1994). [Pg.44]

Dioxin (2,3,7,8-TCDD) zero 0.00000003 Reproductive difficulties increased risk of cancer Emissions from waste incineration and other combustion discharge from chemical factories... [Pg.21]

The plant s product was hexachlorophene, a bactericide, with trichlorophenol produced ns an intermediate. During normal operation, a very small amount of TCDD (2,3,7,8 telrachlomdib zoparadioxin) is produced in the reactor as an undesirable side product. TCDD is perhaps the most ]in(enl toxin known to man. Studies have shown TCDD to be fatal in doses as small as lE-9 times die body weight, it insolubility in water makes decontamination very difficult. Nonlethal doses of TCDD result in chloracne, an acne-like disea.se that can persist for several years. [Pg.251]

A similar rclea.se occurred in Duphar, India in 1963, after which the plant was disassembled brick by brick, encased in concrete and dumped into the ocean. Less than 200 grams of TCDD w ere released at Duphar, and the contamination was confined to the plant. Fifty men did the clean nn four eventually died from the exposure. [Pg.251]

There are even receptors that are known to become activated only due to interaction with a synthetic chemical, and no physiological agonist for such a receptor has been characterized. A model receptor in this class is the so-called Ah receptor complex that becomes activated subsequent to its exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxiu (TCDD). Activation of the. Ah receptor... [Pg.279]

Chemical Acne Many chemical compounds induce skin lesions that are similar to acne. Oils, tar, creosote, and several cosmetic products induce chemical acne. These compounds induce keratinization of the sebaceous glands of the skin, obstruction of the glands, and formation of acne. Chloracne is a specific skin lesion that is induced by chemical compounds that are structurally similar to 2,5,7,8-tet-rachloro dibenzo-p-dioxin (TCDD). Chloracne is slow to heal and difficult to... [Pg.307]

TCDD is the most potent inducer of chloracne. This has been well known since the accident in Seveso, Italy, in 1976 in which large amounts of TCDD were distributed in the environment subsequent to an explosion in a factory that produced a chlorophenoxy herbicide, 2,4,5-T. TCDD is an impurity produced during the production of 2,4,5-T. The most common long-term effect of TCDD exposure was chloracne. Exposed individuals also suffered increased excretion of porphyrins, hyper-pigmentation, central nervous system effects, and liver damage and increased risk of cancer was a long-term consequence of the exposure. In addition to TCDD, polychlorinated biphenyls (PCBs), polychlorinated dibenzofurans, and polychloronaphthalens cause chloracne as well as other effects typical of TCDD. 7i... [Pg.309]

FAS is normally characterized by growth retardation, anomalies of the head and face, and psychomotor dysfunctions. Excessive consumption of ethyl alcohol may lead to malformations of the heart, extremities, and kidneys. Since consumption of ethyl alcohol is socially acceptable and prevalent even in pregnant women, the risks associated with the use of ethyl alcohol are remarkable. However, it should be kept in mind that there are several chemical compounds in tlie occupational environment that may also cause malformations even at low doses. The oc-cupationally-important known human teratogens include methyl mercury, ethyl alcohol, PCB compounds, tobacco smoke, lead, TCDD, 2,4,5- F, carbon monoxide, nitrogen dioxide, gasoline, and fluoride. [Pg.316]

As shown by several investigations [91], the bromine-rich polybromide phase by itself is hardly flammable and fireextinguishing properties have been reported occasionally. The formation of polybrominated dibenzo-dioxins (PBrDD) and furans (PBrDF) due to the plastic-containing housing of a zinc-flow battery cannot be totally neglected in the case of a fire, but their concentrations are far away from the tetrachloro dibenzodioxine (TCDD) toxic equivalents even in a worst-case scenario. [Pg.191]


See other pages where 2,3,7,8-TCDD is mentioned: [Pg.963]    [Pg.963]    [Pg.963]    [Pg.971]    [Pg.971]    [Pg.238]    [Pg.280]    [Pg.241]    [Pg.421]    [Pg.223]    [Pg.65]    [Pg.66]    [Pg.66]    [Pg.2211]    [Pg.189]    [Pg.19]    [Pg.20]    [Pg.20]    [Pg.6]    [Pg.6]    [Pg.8]    [Pg.111]    [Pg.148]    [Pg.251]    [Pg.280]    [Pg.281]    [Pg.324]    [Pg.46]    [Pg.49]    [Pg.51]    [Pg.51]    [Pg.52]    [Pg.52]    [Pg.53]    [Pg.604]   
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2,3,7,8-Tetrachlorodibenzo-p-dioxin TCDD)

2,3,7,8-Tetrachlorodibenzo-para-dioxin 2,3,7,8-TCDD)

2,3,7,8-Tetrachlorodibenzodioxin TCDD)

2,3,7,8-tetrachIorodibenzo-p-dioxin TCDD)

2,3,7,8-tetrachlorodibenzo-/>-dioxin TCDD)

2.3.7.8- TCDD compounds

2.3.7.8- Tetrachloro TCDD

Acceptable daily intake 2 ,3,7 ,8-TCDD

Adipose tissue 2,3,7,8-TCDD levels

Arkansas 2.3.7.8- TCDD contamination

Aryl hydrocarbon hydroxylase 2,3,7,8-TCDD

Aryl hydrocarbon hydroxylase induction, 2,3,7,8-TCDD

Aryl hydrocarbon receptor, TCDD

Bioaccumulation TCDD study

Bioavailability 2 ,3,7,8-TCDD from contaminated

Bioconcentration of 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD)

Bone marrow, TCDD

Concentration, 2,3,7,8-TCDD

Concentration, 2,3,7,8-TCDD plants

Conjugation TCDD metabolism

Dioxins/TCDD

Dioxins/TCDD bioassays

Dioxins/TCDD endocrine disruption

Dioxins/TCDD environmental fate

Dioxins/TCDD enzyme induction

Dioxins/TCDD formation

Dioxins/TCDD herbicide contaminants

Dioxins/TCDD metabolism

Dioxins/TCDD reductive

Ecological Effects Related to TEQs for 2,3,7,8-TCDD

Exposure, TCDD

Exposures to TCDD

Fish, 2,3,7,8-TCDD contamination

Guinea pigs, 2,3,7,8-TCDD

Guinea pigs, 2,3,7,8-TCDD toxicity

Hamster, 2,3,7,8-TCDD

Hamster, 2,3,7,8-TCDD toxicity

Human 2,3,7,8-TCDD

Human TCDD analysis

Human health effects 2.3.7.8- TCDD

Humans TCDD exposure

Indicator approach, 2,3,7,8-TCDD

Metabolism of TCDD

Mobility, 2,3,7,8-TCDD

Oxidation, 2,3,7,8-TCDD

Phenoxy acids, TCDD

Photodegradation, 2,3,7,8-TCDD

Plants 2,3,7,8-TCDD

Polychlorinated dibenzodioxins 2 ,3 ,7,8-TCDD

Proteins TCDD complex

Recovery, TCDD

Soil-water partition 2,3,7,8-TCDD

Species differences TCDD toxicity

Species, 2,3,7,8-TCDD toxicity

Superfund sites TCDDs

TCDD (2,4,7,8-tetrachlorodibenzo

TCDD contamination

TCDD equivalent quantity

TCDD receptor

TCDDs

Tetra-chlorodibenzo-p-dioxin TCDD)

Thymus, TCDD

Toxic equivalency factors TCDDs

Toxicity of 2,3,7,8-TCDD

Transport processes 2,3,7,8-TCDD

Vapor pressure 2,3,7,8-TCDD

Volatilization, 2,3,7,8-TCDD

Water solubility 2.3.7.8- TCDD

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