Examples of 'glycidyl' in a sentence
Meaning of "glycidyl"
Glycidyl (noun): A chemical compound commonly used in the production of resins and plastics
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- The univalent radical derived from glycidol
How to use "glycidyl" in a sentence
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glycidyl
Glycidyl fatty acid esters expressed as glycidol.
Preference is given to glycidyl methacrylate as unsaturated epoxide.
Glycidyl acrylate and glycidyl methacrylate are preferred.
It is preferred to use glycidyl methacrylate as unsaturated epoxide.
Particularly preferred are resins of the glycidyl type.
Preferred is the glycidyl ester of neodecanoic acid.
Another useful class of monoepoxides are glycidyl ethers.
Examples are glycidyl adipate and glycidyl phthalate.
In particular the polyfunctional glycidyl ethers are useful.
Such glycidyl ethers are preferably monoepoxide compounds.
The resultant product is a glycidyl amine compound.
Methyl and glycidyl methacrylates are very particularly preferred.
The resultant product is a glycidyl ether compound.
Glycidyl functional silanes would be used in this case.
Another useful class of monoepoxides is glycidyl ethers.
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Use is preferably made of glycidyl methacrylate as unsaturated epoxide.
A preferred crosslinking monomer is allyl glycidyl ether.
No glycidyl species were detectable by gas chromatography.
Process for the preparation of glycidyl polyethers of polyphenols.
Glycidyl acrylate is the preferred reactant.
Bireactive monomers such as glycidyl methacrylate are also useful.
Allyl glycidyl ether is particularly preferred among them.
Particularly preferred compounds are glycidyl acrylate or glycidyl methacrylate.
Glycidyl acrylate and glycidyl methacrylate are particularly suitable.
Epoxy groups include glycidyl and glycidyloxy groups.
Glycidyl methacrylate is an epoxy base monomer.
The termonomer is preferably glycidyl methacrylate.
Amino or glycidyl functional silanes are preferred.
The comonomer is preferably glycidyl methacrylate.
Glycidyl methacrylate is preferred as ethylenic monomer bearing an epoxy function.
Preferred acrylates are hydroxypropyl acrylate and glycidyl methacrylate.
Preparation of glycidyl polyethers of polyphenols.
The epoxides that are especially preferred are glycidyl ethers.
Allyl glycidyl ether is preferred.
Of particular interest are glycidyl ethers of phenols.
Glycidyl acrylate and glycidyl methacrylate are used most often.
Another example is nonylphenyl glycidyl ether.
The glycidyl ethers of various phenolic compounds are particularly important.
Essentially quantitative conversion of glycidol to glycidyl acetoacetate was confirmed.
Glycidyl methacrylate is particularly suitable.
Alkylating groups of the crosslinkers are preferably glycidyl groups.
Preparation of glycidyl acrylate resin.
Manufacture of epoxyethyl ethers or glycidyl ethers.
It is preferred to use glycidyl compounds having two functional groups.
Glycidyl esters are also typically present as esters of fatty acids.
Most preferred is glycidyl methacrylate.
Glycidyl methacrylate is particularly preferred.
The contemplated epoxy resins are glycidyl ethers of polyhydroxy compounds.
Preferred reactive terminal ether portions include glycidyl ether.
The epoxide compound preferably is glycidyl methacrylate or glycidyl acrylate.
