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Fluoride in the environment

So far only a few dozen organofluorine compounds have been isolated from living organisms, for example fluoroacetic acid, 4-fluorothreonine and rw-fluoro-oleic acid [244-246], The reason that nature has not invested in fluorine chemistry could be a combination of low availability of water-dissolved fluoride in the environment due to its tendency to form insoluble fluoride salts, and the low reactivity of water-solvated fluoride ion. However, in 2002, O Hagan and collaborators [247] published the discovery of a biochemical fluorination reaction in a bacterial protein extract from Streptomyces cattleya converting S-adenosyl-L-methionine (SAM) to 5 -fluoro-5 deoxyadenosine (5 -FDA). The same protein extract contained also the necessary enzymatic activity to convert 5 -FDA into fluoroacetic acid. In 2004, the same authors published the crystal structure of the enzyme and demonstrated a nucleophilic mechanism of fluorination [248,249]. [Pg.44]

A.W. Davison, L.H. Weinstein, Some problems relating to fluorides in the environment Effects on plants and animals, in A. Tressaud (Ed.), Advances in Fluorine Science, Vol. 1, Elsevier, Amsterdam, 2006, pp. 251-298. [Pg.540]

H.L. Weinstein, Fluorides in the Environment Effects on Plants and Animals, CABI, Cambridge, MA, USA, 2004. [Pg.117]

The aim of this section is to present a concise overview of separation, concentration and decomposition methods for sample pre-treatment and an overview of the analytical methods available for determining free inorganic fluoride and total fluorine in the environment (natural and drinking water, air and soil), biological and related materials, and fluoride supplements and dental products. [Pg.533]

P.S. Low, H. Bloom, Atmospheric deposition of fluoride in the lower Tamar Valley, Tasmania, Atmos. Environ. 22 (1988) 2049-2056. [Pg.540]

How can compounds be recognized as mutagenic This is an important question that is difficult to answer and which has led to many controversies. For example, how dangerous is formaldehyde in the environment 801 Butadiene 802 Dioxin 790,803 Is fluoride a carcinogen 804,805... [Pg.1589]

Aluminum occurs widely in nature in silicates such as micas and feldspars, complexed with sodium and fluorine as cryolite, and in bauxite rock, which is composed of hydrous aluminum oxides, aluminum hydroxides, and impurities such as free silica (Cotton and Wilkinson 1988). Because of its reactivity, aluminum is not found as a free metal in nature (Bodek et al. 1988). Aluminum exhibits only one oxidation state (+3) in its compounds and its behavior in the environment is strongly influenced by its coordination chemistry. Aluminum partitions between solid and liquid phases by reacting and complexing with water molecules and anions such as chloride, fluoride, sulfate, nitrate, phosphate, and negatively charged functional groups on humic materials and clay. [Pg.210]

Given the implications involved in fluoride contamination in the environment, the development of... [Pg.83]

Pasture grasses and small grains are symptom-free even at leaf concentrations of several hundred parts per million of fluoride. Thus, the absence of injury symptoms on a plant does not necessarily mean that this plant has not been exposed to a pollutant in the environment in which it is growing, and such a symptomless plant may actually contain high concentrations of a pollutant like F. The accumulated fluoride is not evenly distributed, but tends to accumulate in the leaf tips and margins (18, 23, 24). Tips of oat leaves may contain 10-100 times as much F as the basal portion (15). [Pg.34]

Recently, we can witness many discussions about the benefits and risks of the fluoride supplementation. Also the question of aluminum toxicity in men has been discussed. The understanding of the mechanisms of their synergistic action could allow us to explain numerous observations about the effects of increased load of fluoride and aluminum in the environment and to reevaluate their widespread use. Understanding the role of phosphate and G-proteins in cell signaling forces us to accept the fact that aluminum in the environment, water, and food chains followed by fluoride ions could evoke various and multiple pathological symptoms. [Pg.177]

Fluorine is not destroyed in the environment, but rather it combines with minerals to form salts, which remain in the soil. Hydrogen fluoride gas is absorbed into the atmosphere to form hydrofluoric acid, which eventually returns to earth in the form of precipitation. Fluorides form strong associations with sediment and soil particles, which eventually accumulate in plants and the bones and/or shells of animals. [Pg.1157]

Fluorides emitted into the atmosphere from different sources include both gaseous and particulate forms. Historically, most of the F pollution problems occurred as a result of emissions from anthropogenic sources. Such emissions occasionally resulted in the presence of harmful levels of F compounds in the environment as well as in body tissues. The forms of F emitted from these sources include hydrogen fluoride, cryolite, fluorspar, and silicon tetrafluo-ride (SiF4). The anthropogenic sources also contribute F to surface waters. [Pg.205]

Ekstrand J, Oliveby A Fluoride in the oral environment. Acta Odontol Scand 1999 57 330-333. Fejerskov O, Thylstrup A, Larsen MJ Rational use of fluorides in caries prevention. A concept based on possible cariostatic mechanisms. Acta Odontol Scand 1981 39 241-249. [Pg.147]

One of the crucial problems in the chemistry of potassium hexafluorotitanate, K2Tip6, is its stability in the environment of different alkali metal fluorides and/or chlorides, since these compounds are usually used as complementary electrolyte components. The cryoscopic measurements in a system containing alkali metal halides and K2Tip6 make it possible to determine the dissociation scheme of K2TiPe, or other reactions taking place between alkali metal halides and K2TiPe. The study of some systems of this type can be found in the literature. [Pg.43]

Xenobiotics enter in the bloodstream, following one of the described absorption routes, are distributed into the body and undertaken by different organs. It is possible that a part of the xenobiotics distributed into the body may be stored in tissues or even in the blood. A word commonly used to refer to storage of a pollutant at higher levels than those found in the environment is bioaccumulation, for example, PAHs, PCBs, dioxins and some organometallic forms of metals bioaccumulate in fat, fluoride and lead in bones etc. Sometimes biomagnification takes place, as a bioaccumulation process within the trophic chain, in indirect relationship with biota. [Pg.258]

Clinical manifestations of fluorosis often occur in the hard tissues of animals, such as bones and teeth, as a result of long-term intake of elevated levels of fluoride, mainly due to industrial fluoride pollution. Evidence also indicates harmful effects of fluoride on soft tissues such as lung, kidney, testis, fiver and brain. Generally, fluorine, in the form of the fluoride ion (F ), is present in soil and water in low concentrations, but it may cause a threat to public and occupational health when its presence in the environment increases due to natural or anthropogenic sources. Excessive intake of F via drinking water is an endemic problem in a number of countries including China, India,... [Pg.643]

Because fluorides are found naturally in the environment, we cannot avoid being exposed to them. [Pg.189]

B. Pharmacokinetics. Fluoride is a weak acid (pKa 3.4) that is passively absorbed from the stomach and small intestine. In an acidic environment more fluoride is present as HF, which is more rapidly absorbed. Fasting peak absorption occurs in 30-60 minutes. The volume of distribution is 0.5-0.7 Ukg. Fluoride Is not protein bound, but binds readily to magnesium and calcium in blood, tissues, and bone (most fluoride in the body is bound to bone). The elimination half-life is 2.4-4.3 hours and is prolonged in patients with renal failure. [Pg.200]

Polyacid-modified composite resins have undergone considerable development since they first appeared. The very limited nature of the acid-base reaction means that they have had to have the fluoride-releasing capability augmented, for example, through the inclusion of extra ytterbium fluoride in the formulation [38]. There has also been concern that the abihty to draw in water from the environment might also lead to staining and softening, and reformulation has partly been driven by the need to minimize any such moisture uptake, so as to preserve the physical properties of the composite. [Pg.27]


See other pages where Fluoride in the environment is mentioned: [Pg.11]    [Pg.492]    [Pg.140]    [Pg.167]    [Pg.1155]    [Pg.2]    [Pg.11]    [Pg.492]    [Pg.140]    [Pg.167]    [Pg.1155]    [Pg.2]    [Pg.36]    [Pg.780]    [Pg.116]    [Pg.166]    [Pg.217]    [Pg.82]    [Pg.184]    [Pg.167]    [Pg.418]    [Pg.290]    [Pg.28]    [Pg.1155]    [Pg.2579]    [Pg.127]    [Pg.110]    [Pg.94]    [Pg.1416]    [Pg.527]    [Pg.417]    [Pg.270]    [Pg.138]    [Pg.26]   
See also in sourсe #XX -- [ Pg.490 , Pg.491 , Pg.492 ]




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