Examples of 'caprolactone' in a sentence
Meaning of "caprolactone"
Caprolactone is a cyclic ester compound used in polymer synthesis and various industrial applications
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- A cyclic ester with the chemical formula C₆H₁₀O₂
How to use "caprolactone" in a sentence
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caprolactone
Another useful reactive monomer may be caprolactone.
The major use of caprolactone is the production of polycaprolactones.
An example of a cyclic ester that may be used is caprolactone.
Caprolactone can be cited as an example of a lactone.
Other hydroxyalkylacrylates such as caprolactone acrylate are mentioned.
Caprolactone oligomers may be also used.
Lactams and lactones are in particular caprolactam and caprolactone.
Epsilon caprolactone is particularly preferred.
The larger peak belongs to the caprolactone segment.
Caprolactone is amongst others a useful product to prepare caprolactam from.
The minor component comprises copolymers containing caprolactone.
Caprolactam can be prepared from caprolactone in a manner known per se.
The caprolactone was not redistilled.
The product then can be converted into caprolactone.
Caprolactone is advantageously used.
See also
Examples are caprolactame and caprolactone.
Copolymers of lactide and caprolactone yield less acidic degradation products.
Particularly useful synthetic bioabsorbable polymers contain caprolactone linkages.
Hydroxyl terminated polycaprolactones can be formed by reaction of a caprolactone with a glycol.
Specific examples of suitable lactones include caprolactone and valerolactone.
Caprolactone and hydroxypivalic acid are also useful if good weather resistance is desired.
The flask was shaken to dissolve the catalyst in the caprolactone.
Also hydroxy functional adducts of caprolactone and hydroxyalkyl acrylates and methacrylates.
Caprolactone is preferred.
Gas chromatography showed that all the caprolactone had been consumed.
The epsilon caprolactone employed in accordance with the present invention is commercially available.
Preference is given to caprolactone.
Caprolactone and hydropivalic acid can also be used if good weather resistance is required.
Monoacid functional polyesters of lauric acid and caprolactone can be used.
The use of caprolactone oligomer polyols derived from acyclic polyols has been recommended.
Polyesters derived from cyclic esters such as caprolactone are also suitable.
Some polyester polyols employ caprolactone or dimerized unsaturated fatty acids in their manufacture.
One can also use selected hydroxyalkylcarboxylic acids or a lactone such as caprolactone.
By using a slightly higher percentage of caprolactone in the formulation the open time has improved.
Alternatively polyesters can be prepared from ring opening polymerizations of lactones such as caprolactone.
Some polyester polyols also employ caprolactone and dimerized unsaturated fatty acids in their manufacture.
The polymer stent is preferably formed of two polymers comprising a lactide and a caprolactone.
One part of a caprolactone segment can react with four parts of a lactic acid polycondensate segment.
The minor component may include copolymers containing biodegradable monomers such as caprolactone.
Complete reaction between the caprolactone segments and the lactic acid polycondensate segments was assumed.
Recently a wide range of catalysts for the ring opening polymerization of caprolactone have been reviewed.
Caprolactone provides divalent pentyl radical having two free valencies connected to a divalent internal ester group.
The block copolymer has one or more blocks manufactured from the monomer caprolactone.
The polycaprolactone polymers utilized herein are typically derived from linear polyester diols derived from caprolactone.
The latter product is a linear polyester with a high molecular weight derived from a caprolactone monomer.
Another process for the homopolymerization of caprolactone has been described by Maigorzata Basko et al.
A bioabsorbable coating for a surgical article comprises a polymer manufactured from at least the monomer caprolactone.
These polyadducts comprising caprolactone and dioxane are abbreviated PDC in the following.
Component D used in particular preference is epsilon caprolactone.
Polyesters on the basis of e - caprolactone are also suitable.
