Examples of 'perfluoroalkyl' in a sentence
Meaning of "perfluoroalkyl"
perfluoroalkyl (noun) - A type of synthetic chemical compound that contains fluorine atoms and carbon atoms fully saturated with fluorine. These compounds are used in a variety of industrial applications
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- Any perfluoro derivative of an alkyl group.
How to use "perfluoroalkyl" in a sentence
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perfluoroalkyl
Also suitable are perfluoroalkyl acrylates and methacrylates.
Substituted polymers advantageously comprise perfluoroalkyl chains.
Is chosen from perfluoroalkyl radicals and perfluoroaryl radicals.
Process for the preparation of perfluoroalkyl ketones.
Examples of perfluoroalkyl groups are pentafluoroethyl or trifluoromethyl.
The aforesaid fluoroalkyl groups are preferably perfluoroalkyl groups.
The perfluoroalkyl alkyl silanes are preferably applied in solution.
Perfluoropolyethers having perfluoroalkyl end groups.
Perfluoroalkyl betaine gives good quality and stable foams.
The fluoroalkyl groups are most preferably perfluoroalkyl groups.
Classes of perfluoroalkyl sulfonate substances.
The aliphatic group is highly preferably alkyl or perfluoroalkyl.
Manufacture of solid perfluoroalkyl bromides.
Perfluoroalkyl groups are particularly preferred.
Process for the preparation of iodoalcohols having a perfluoroalkyl chain.
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Silicone or perfluoroalkyl derivatives are particularly effective in deactivating skin adhesives.
A common characteristic of perfluoropolyethers is the presence of perfluoroalkyl ether moieties.
By perfluoroalkyl group is meant a saturated branched or linear carbon chain.
Describes fluorinated paper sizes which are copolymers of perfluoroalkyl acrylate.
Examples of perfluoroalkyl as used herein include trifluoromethyl and pentafluoroethyl.
Rf group is preferably a perfluoroalkyl group.
Most preferably the perfluoroalkyl group is a perfluorobutylethyl group or the like.
It is present in an amount suitable to stabilize the perfluoroalkyl alkyl ketone.
Synthesis of perfluoroalkyl bromides.
The perfluoroalkyl group includes trifluoromethyl group and pentafluoroethyl group.
Trifluoropropyl groups or perfluoroalkyl groups.
Perfluoroalkyl thiols useful herein are well documented in the prior art.
Structures contain a hydrophobic perfluoroalkyl backbone and a hydrophillic end group.
Perfluoroalkyl thiols useful herein as well documented in the prior art.
Synthesis of perfluoroalkyl iodides.
Conventional iodine chain transfer agents include alkyl or perfluoroalkyl iodides.
The subject perfluoroalkyl oxetanes are readily isolated in high yield and purity.
The surfactant of choice in the synthesis of fluoropolymers is generally a perfluoroalkyl surfactant.
With perfluoroalkyl groups it is meant alkyl groups fully substituted by fluorine atoms.
The present invention relates to the stabilization of perfluoroalkyl alkyl ketones.
Other perfluoroalkyl acids with shorter or longer alkyl chain do have similar properties.
The telomer thus formed consists of a perfluoroalkyl chain having a terminal iodine group.
Examples of perfluoroalkyl radicals that may be mentioned include trifluoromethyl and pentafluoroethyl radicals.
The fluorocarbon is preferably a block copolymer of a perfluoroalkyl acrylate and a polyethylene substituted acrylate.
It also includes perfluoroalkyl in which every substitutable hydrogen on alkyl is substituted with fluorine.
The process of the invention concerns the preparation of iodoalcohols having a perfluoroalkyl chain.
Perfluoroalkyl sugars are known for their surfactant properties and their capacity to transport oxygen.
The compositions according to the invention comprise one or more urethane perfluoroalkyl esters.
Haloalkyl can also include perfluoroalkyl wherein all hydrogens of a loweralkyl group are replaced with fluorides.
The fluoroalkyl portion of the fluoroalkylating agent refers to a partially fluorinated or perfluoroalkyl group.
A perfluoroalkyl group is an alkyl group in which all H have been replaced with fluorine.
The organic polymer preferably contains at least one of a perfluoroalkyl group and a silicone group.
R F is a perfluoroalkyl group comprising between one and eight carbon atoms.
The polymerization is perferably carried out in the presence of perfluoropolyethers having perfluoroalkyl end groups.
Increasing perfluorooctanoate PFOA a perfluoroalkyl substance concentrations were also associated with fewer autistic behaviors.