Examples of 'polyglycidyl' in a sentence
Meaning of "polyglycidyl"
Polyglycidyl is a chemical compound or substance that contains multiple glycidyl groups
How to use "polyglycidyl" in a sentence
Basic
Advanced
polyglycidyl
An advanced polyglycidyl amine composition prepared by reacting.
A second component for the gels is a polyglycidyl ether.
The polyglycidyl ether can be hydrophilic or hydrophobic.
Preferred polyepoxides are polyglycidyl ethers of cyclic polyols.
Polyglycidyl esters of polycarboxylic acids are mentioned below.
Preferred polyepoxides are polyglycidyl ethers and polyglycidyl esters.
Polyglycidyl ethers of polyhydroxy compounds are preferred.
The preferred polyepoxides are polyglycidyl ethers of aliphatic alcohols.
Polyglycidyl ethers of polyhydric alcohols are also suitable as epoxy resins.
It is also possible to use mixtures of said polyglycidyl compounds.
A preferred type of polyol polyglycidyl ether is a polyol triglycidyl ether.
Polyglycidyl esters of polyacids are also useful in the present invention.
Other suitable polyepoxides include polyglycidyl ethers of polyhydric alcohols.
Sorbitol polyglycidyl either is preferred since it forms a high quality finish.
Another class of polyepoxides are the polyglycidyl esters of polycarboxylic acids.
See also
Polyglycidyl azides comprising an acyloxy terminal group and an azide terminal group.
It is desirable that the polyglycidyl ether component is also hydrophilic.
The polyglycidyl ethers of the invention are prepared by glycidating a hydroxyalkyl carbamate compound.
Advantageously the epoxy resin is a polyglycidyl ether of a dihydric phenol.
Bisphenol polyglycidyl ethers are prepared conventionally by the reaction of bisphenols with epichlorohydrin.
Preferably the epoxy resin is a polyglycidyl ether of a polyhydric phenol.
A second component for the gels of the present invention is a polyglycidyl ether.
Further suitable epoxide prepolymers are polyglycidyl ethers of polyalcohols or diamines.
The use of polyglycidyl ethers of polyhydric alcohols as the polyepoxide is disclosed but discouraged.
Another class of epoxy resins are the polyglycidyl ethers of polyhydric alcohols.
Contacting the bioprosthetic material with a mixture containing at least two polyglycidyl ethers.
The inherent flow capacity of the polyglycidyl polyethers is substantially enhanced.
Aromatic epoxy resins include epoxy group containing aromatic polyglycidyl ethers.
Examples of such epoxides are polyglycidyl ethers of polyhydric phenols and of aliphatic alcohols.
Multifunctional carbonate compounds have traditionally been formed using polyglycidyl ethers as starting materials.
The preferred polyepoxides are polyglycidyl ethers of polyhydric alcohols such as cyclic polyols.
The epoxy resin compositions according to the invention especially comprise a liquid polyglycidyl ether or ester.
Further examples of such polyepoxides are polyglycidyl ethers of polyhydric phenols and of aliphatic alcohols.
Such polyglycidyl aromatic amines can be prepared by reacting the corresponding polyaromatic amine with epichlorohydrin.
Another class of epoxide resins are the polyglycidyl esters of polycarboxylic acids.
The above polyglycidyl compounds can be cured using either basic or acidic curing agents.
Examples of other suitable polyepoxides include polyglycidyl esters of polycarboxylic acids.
Contacting the bioprosthetic material with a mixture of ethylene glycol diglycidyl ether and glycerol polyglycidyl ether.
Other suitable polyepoxide resins include polyglycidyl ethers of polyhydric alcohols.
Polyglycidyl ethers of bisphenol A and glycidylamines are especially preferred.
Also useful are the polyepoxides which are polyglycidyl ethers of polycarboxylic acids.
In another embodiment component B comprises epoxy resin precursor a polyglycidyl.
Further polyepoxides suitable in principle are the polyglycidyl ethers of polyalcohols or diamines.
The preferred polyglycidyl ethers are polyglycidyl ethers of bisphenol A and similar polyphenols.
A particularly suitable epoxy resin is based on a polyglycidyl ether of a polyhydric phenol.
Polyglycidyl ethers of bisphenol A are especially preferred.
By way of example there may be mentioned the polyglycidyl ethers of polyhydroxylated compounds.
Polyglycidyl ethers of bisphenol A and polyglycidyl ethers of bisphenol F are especially preferred as component b.
Also useful are the epoxide resins which are polyglycidyl esters of polycarboxylic acids.
The preferred polyglycidyl ether is the diglycidyl ether of Bisphenol A.
