Fluorotelomer Ethoxylate
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Fluorotelomers are
fluorocarbon Fluorocarbons are chemical compounds with carbon-fluorine bonds. Compounds that contain many C-F bonds often have distinctive properties, e.g., enhanced stability, volatility, and hydrophobicity. Several fluorocarbons and their derivatives are ...
-based
oligomers In chemistry and biochemistry, an oligomer () is a molecule that consists of a few repeating units which could be derived, actually or conceptually, from smaller molecules, monomers.Quote: ''Oligomer molecule: A molecule of intermediate relativ ...
, or telomers, synthesized by telomerization. Some fluorotelomers and fluorotelomer-based compounds are a source of environmentally persistent perfluorinated carboxylic acids such as
PFOA Perfluorooctanoic acid (PFOA; conjugate base perfluorooctanoate; also known colloquially as C8, from its chemical formula C8HF15O2) is a perfluorinated carboxylic acid produced and used worldwide as an industrial surfactant in chemical process ...
and
PFNA Perfluorononanoic acid, or PFNA, is a synthetic perfluorinated carboxylic acid and fluorosurfactant that is also a persistent organic pollutant. Chemistry and properties In acidic form it is a highly reactive strong acid. In its conjugate base for ...
, while others are under extended investigation.


Types

There are many broad categories of fluorotelomers: * Fluorotelomer alcohols (FTOH) * Fluorotelomer ethoxylates (FTEO) * Fluorotelomer fumarates * Fluorotelomer methacrylates (FTMAC) * Fluorotelomer sulphonates (FTS)


Production

In the radical telomerization of fluorotelomer
molecule A molecule is a group of two or more atoms that are held together by Force, attractive forces known as chemical bonds; depending on context, the term may or may not include ions that satisfy this criterion. In quantum physics, organic chemi ...
s, a variety of fluorinated
alkenes In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond. The double bond may be internal or at the terminal position. Terminal alkenes are also known as Alpha-olefin, α-olefins. The Internationa ...
can serve as unsaturated taxogens including
tetrafluoroethylene Tetrafluoroethylene (TFE) is a fluorocarbon with the chemical formula . It is a colorless gas. Its structure is . It is used primarily in the industrial preparation of fluoropolymers. It is the simplest perfluorinated alkene. It was first repor ...
, vinylidene fluoride, chlorotrifluoroethylene, and hexafluoropropene. However, many fluorotelomers, such as fluorotelomer alcohols, are
fluorocarbon Fluorocarbons are chemical compounds with carbon-fluorine bonds. Compounds that contain many C-F bonds often have distinctive properties, e.g., enhanced stability, volatility, and hydrophobicity. Several fluorocarbons and their derivatives are ...
-based because they are synthesized from tetrafluoroethylene. In addition to alcohols, synthetic products include fluorotelomer iodides, olefins, and
acrylate Acrylates (IUPAC: prop-2-enoates) are the salts, esters, and conjugate bases of acrylic acid. The acrylate ion is the anion . Often, acrylate refers to esters of acrylic acid, the most common member being methyl acrylate. These acrylates contain ...
monomer A monomer ( ; ''mono-'', "one" + '' -mer'', "part") is a molecule that can react together with other monomer molecules to form a larger polymer chain or two- or three-dimensional network in a process called polymerization. Classification Chemis ...
.
Polymer A polymer () is a chemical substance, substance or material that consists of very large molecules, or macromolecules, that are constituted by many repeat unit, repeating subunits derived from one or more species of monomers. Due to their br ...
ized acrylate from iodide and alcohol monomers represent >80% of the global manufacture and use of fluorotelomer-based products.


Applications

Fluorotelomers are used in fire-fighting foams, grease-resistant food packaging, leather protectants and stain-resistant carpeting, textiles, anti-fogging sprays and wipes. Fluorotelomers are applied to food contact papers for their
lipophobicity Lipophobicity, also sometimes called lipophobia (from the Greek λιποφοβία from λίπος ''lipos'' "fat" and φόβος ''phobos'' "fear"), is a chemical property of chemical compounds which means " fat rejection", literally "fear of fa ...
, making paper resistant to absorbing oil from fatty foods. Fluorotelomer coatings are used in microwave popcorn bags, fast food wrappers, candy wrappers, and pizza box liners.


Environmental and health concerns

Fluorotelomers that contain PFOA precursors can be metabolized into, and degrade to, PFOA, a persistent global contaminant found in people in the low-
parts per billion In science and engineering, the parts-per notation is a set of pseudo-units to describe the small values of miscellaneous dimensionless quantities, e.g. mole fraction or mass fraction. Since these fractions are quantity-per-quantity measur ...
range. Toxicologists estimate microwave popcorn, because of the high heat and coated bag, could account for about 20% of the PFOA levels measured in an individual consuming 10 bags a year if 1% of the fluorotelomers are metabolized to PFOA. PFOA is also formed as an unintended byproduct in the production of fluorotelomers, and is thus present in finished goods treated with fluorotelomers, including those intended for food contact. In a U.S. Food and Drug Administration (USFDA) study, fluorotelomer-based paper coatings (which can be applied to food contact paper in the concentration range of 0.4%) were found to contain 88,000–160,000
parts per billion In science and engineering, the parts-per notation is a set of pseudo-units to describe the small values of miscellaneous dimensionless quantities, e.g. mole fraction or mass fraction. Since these fractions are quantity-per-quantity measur ...
PFOA, while microwave popcorn bags contained 6–290 parts per billion PFOA.


Industry and government actions

In 2002
Burger King Burger King Corporation (BK, stylized in all caps) is an American multinational chain store, chain of hamburger fast food restaurants. Headquartered in Miami-Dade County, Florida, the company was founded in 1953 as Insta-Burger King, a Jacks ...
stopped using fluorotelomer coated boxes. After more than a year of negotiating with " telomer makers Asahi Glass, Clariant, Daikin America, and DuPont to perform degradation studies on 13 of their products", the U.S. Environmental Protection Agency (USEPA) and companies were not able to agree on terms. Thus, in late June 2004 the USEPA announced it would perform the degradation studies itself, with an expected time to complete the studies of 1 year. However, in a December 2005 deal with the USEPA over alleged withholdings, DuPont agreed to test nine of its fluorotelomer-based products' potential to break down into PFOA by 27 December 2008. Yet, in late December 2008, the USEPA and DuPont filed a joint motion stating that DuPont needed additional time to purify the products. USEPA lawyers extended the deadline by three years, to 27 December 2011, in the last month of the Bush administration. In 2009 a 546-day USEPA study was published that estimated a degradation half-life for a fluorotelomer-based polymer in the range of 10–17 years. This estimate was much shorter than the half-life estimated by a DuPont study. Given this discrepancy, the USEPA undertook an extensive effort to develop methods for testing the degradation rate of commercial fluorotelomer-based polymers. The USEPA then carried out studies with two DuPont polymers in four soils and water using these methods. These new studies reported half-life ranges for these commercial fluorotelomer-based polymers of 33 to 112 years, roughly consistent with EPA's 2009 estimate.


References

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External links


Perfluorooctanoic Acid (PFOA); Fluorinated Telomers enforceable consent agreement development
Organofluorides Oligomers