Examples of 'acrylates and methacrylates' in a sentence
Meaning of "acrylates and methacrylates"
Acrylates and methacrylates refer to compounds that contain acrylic acid or methacrylic acid. These compounds are commonly used in the production of various plastics, adhesives, and paints due to their ability to polymerize easily
How to use "acrylates and methacrylates" in a sentence
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acrylates and methacrylates
Also suitable are perfluoroalkyl acrylates and methacrylates.
Acrylates and methacrylates.
The term acrylate encompasses acrylates and methacrylates.
Most acrylates and methacrylates have similarly high glass transition temperatures.
Other suitable compounds are melamine acrylates and methacrylates.
Combinations of acrylates and methacrylates can also be used.
Desired ethylenically unsaturated monomers include acrylates and methacrylates.
Preferred alkyl acrylates and methacrylates are listed above.
The term acrylate is meant to encompass acrylates and methacrylates.
Examples of acrylates and methacrylates include trimethylpropane triacrylate and pentaerythritol tetraacrylate.
Useful amino functional monomers include aminoalkyl acrylates and methacrylates.
These acrylates and methacrylates excepting methyl methacrylate may be used alone or in admixture thereof.
Useful free radical polymerizable components include acrylates and methacrylates.
Preferred monomers include alkyl acrylates and methacrylates with methyl methacrylate being particularly preferred.
The term acrylate is used here to encompass both acrylates and methacrylates.
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Examples of such monomers include acrylates and methacrylates such as trimethylolpropane trimethacrylate or trimethylolpropane triacrylate.
Examples given of these ethylenically unsaturated monomers are alkyl acrylates and methacrylates.
Suitable monomers may include the acrylates and methacrylates substituted in any desired manner.
Also hydroxy functional adducts of caprolactone and hydroxyalkyl acrylates and methacrylates.
This is especially the case for the acrylates and methacrylates used in the present invention.
Examples of other unsaturated esters which can be copolymerised are the alkyl acrylates and methacrylates.
Aryl acrylates and methacrylates such as benzyl acrylate and benzyl methacrylate also can be used.
Examples of unsaturated esters wherein the acid moiety is unsaturated include acrylates and methacrylates.
Examples of aryl acrylates and methacrylates are phenyl acrylate, phenyl methacrylate, etc.
The present invention relates to a new process for the synthesis of alkylimidazolidone acrylates and methacrylates.
However, different higher alkyl acrylates and methacrylates were used.
Acrylates and methacrylates are preferably obtainable from alcohols having from 1 to 8 carbon atoms.
Summary of the final screening assessment of six substances in the Acrylates and Methacrylates Group.
The alkyl acrylates and methacrylates generally have an alkyl group comprising from 1 to 8 carbon atoms.
Preferred examples are monofunctional, bifunctional or polyfunctional acrylates and methacrylates.
Among the more preferred acrylates and methacrylates are the methylacrylate, ethylacrylate and methylmethacrylate esters.
Examples of non-silicon hydrophobic materials include alkyl acrylates and methacrylates.
The use of acrylates and methacrylates allows for transesterification reactions with hydroxy-containing modifying agents.
Examples of non-silicone hydrophobic materials include alkyl acrylates and methacrylates.
Suitable comonomers are unsaturated acrylates and methacrylates of from 4 to 12 carbon atoms.
One is an optimized mixture of di - and tri-functional monomers and acrylates and methacrylates.
The acrylates and methacrylates are preferably esters with alcohols of 1-8 carbon atoms.
Also dodecyl, tetradecyl, hexadecyl and octadecyl acrylates and methacrylates are particularly suitable.
PEROXAN AZDN is used for the ( co ) polymerization of styrene, vinylchloride, vinylidenechloride, acrylonitrile, acrylates and methacrylates.
Examples of suitable alkyl acrylates and methacrylates are lauryl methacrylate, 2-ethylhexyl methacrylate and n-butyl acrylate.
Plasticizing agents may be esters such, for example, as alkyl acrylates and methacrylates.
Preferably, these urethane acrylates and methacrylates have a molecular weight of less than 5,000.
Suitable acrylic monomers include functional and non-functional acrylates and methacrylates.
The term " acrylate " includes acrylates and methacrylates.
PEROXAN AIVN-PG is used for the ( co ) polymerization of styrene, vinylchloride, vinylidenechloride, acrylonitrile, acrylates and methacrylates.
Specific examples of suitable diluent monomers include the alkyl acrylates and methacrylates e . g methyl methacrylate.
Description of Embodiments In the present invention, the term " ( meth ) acrylate " includes both acrylates and methacrylates.
Herein an overview on the possible polymerization pathways for ethene, acrylates and methacrylates is presented.
The term " ( meth ) acrylate " is defined here as acrylates, methacrylates or combinations of acrylates and methacrylates.
For example, ( meth ) acrylate refers to acrylates and methacrylates.
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Examples of using Methacrylates
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Acrylate functional groups are preferred over methacrylates
Methyl and glycidyl methacrylates are very particularly preferred
Also suitable are perfluoroalkyl acrylates and methacrylates
Examples of using Acrylates
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Aromatic type urethane acrylates are less preferred
Acrylates are notoriously toxic and tend to shrink
They can also comprise polyesters acrylates
