Examples of 'diglycidyl' in a sentence
Meaning of "diglycidyl"
diglycidyl (noun): Diglycidyl refers to a chemical compound containing two epoxide groups, commonly used in the production of epoxy resins
How to use "diglycidyl" in a sentence
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diglycidyl
Neopentyl diglycidyl ether was used as the epoxy.
A currently preferred crosslinker is ethyleneglycol diglycidyl ether.
Diglycidyl esters of organic dicarboxylic acids are furthermore suitable.
Preferred diepoxides are diglycidyl ethers and diglycidyl esters.
Diglycidyl compounds having aromatic structures are mainly used.
Examples of bisphenol epoxies include bisphenol diglycidyl ethers.
Use is predominantly made of diglycidyl compounds having aromatic groups.
More preferred alkyl epoxides include hexanediol diglycidyl ether.
The diglycidyl ethers are preferred.
Epoxy tetrahydrophthalate and diglycidyl hexahydrophthalate.
The diglycidyl ether is a monotropic liquid crystal with a nematic texture.
Suitable polyepoxides also include a diglycidyl ether of dihydric bisphenol.
The diglycidyl ethers of dihydric phenols represent a kn class of epoxy resins.
Polypropylene glycol diglycidyl ether.
Diglycidyl ether is a chemical compound used as a reactive diluent for epoxy resin.
See also
Predominant use is made of diglycidyl compounds containing aromatic structures.
Successive oxidation of the second alkene would produce diglycidyl ether.
Resorcinol diglycidyl ether.
Certain more preferred alkyl epoxides comprise hexanediol diglycidyl ether.
This includes difunctional amine to a diglycidyl ether compound to produce a modified amine.
Diglycidyl esters of dicarboxylic acids are also useful in preparing the invention polymers.
A representative example of an aliphatic epoxy resin is diglycidyl ether of a polyoxyalkylene glycol.
These diglycidyl ethers provide curable resins and have low viscosity.
A preferred glycidyl ether of a cycloalkylene glycol is the diglycidyl ether of cyclohexane diol.
The reaction products of diglycidyl ethers with bisphenols are commonly referred to as upstaged resins.
The curable compositions also contain a condensation product of a bisphenol diglycidyl ether with a tetrabromo bisphenol.
Such diglycidyl ethers are made by reacting epichlorohydrin and a dihydric phenol with caustic.
Typical epoxy resins that are used are the diglycidyl ethers of a polyhydroxy phenol.
The diglycidyl esters of di and polycarboxylic acids are also useful for the present invention.
They can also be prepared by contacting a diglycidyl ether or an epihalohydrin with a difunctional amine.
The diglycidyl ether thus obtained was completely liberated from solvent by heating under reduced pressure.
Commercially available examples include butanediol diglycidyl diacrylate and hexanediol diglycidyl diacrylate.
The diglycidyl ether of bisphenol A is particularly useful.
This example illustrates the preparation of the diglycidyl ether component of the invention composition.
Bisphenol A diglycidyl ether or epoxycresol novolaks are particularly preferred.
Contacting the bioprosthetic material with a mixture of ethylene glycol diglycidyl ether and glycerol polyglycidyl ether.
The syntheses of the diglycidyl ether compounds follow procedures known in the art.
Step of crosslinking the mixture obtained by adding a bisphenol A diglycidyl ether type epoxy resin.
Graft polymer of ethylene glycol diglycidyl ether modified polyallylamine and diallyl dimethyl ammonium chloride.
Not dissolved Polyethylene glycol diglycidyl ether.
Typical difunctional diglycidyl ethers are bisphenol A diglycidyl ether.
The preferred epoxy resin for this invention is a diglycidyl ether of bisphenol A.
A much preferred diglycidyl ether is diglycidyl ether of bisphenol A.
The preferred polyglycidyl ether is the diglycidyl ether of Bisphenol A.
The diglycidyl ethers of bisphenol A are a common form of epoxy resin.
More preferably the polyepoxide is a diglycidyl ether of bishphenol A.
Of these, diglycidyl ether compounds are particularly suitable.
The most widely used epoxy resins are diglycidyl ethers of bisphenol A.
Diglycidyl ethers of bisphenol-A are particularly preferred.
A preferred resin is a diglycidyl ether of Bisphenol A.
