6-prop-2-enoyloxyhexyl prop-2-enoate

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Using the compositions obtained in Examples 2 to 5 and 7, the following mixture was prepared. That is, the mixture of 100 g (content of fine polymer particles: 5 g) in total, composed of the composition of 7.7 g of Example 2, isobornyl acrylate of 56.35 g, the composition of 5 g of Example 3, tetrahydrofurfuryl acrylate of 0.5 g, the composition of 2 g of Example 4, hydroxyethyl methacrylate of 8 g, the composition of 5 g of Example 5, 1,6-hexanediol diacrylate of 5.25 g, the composition of 5 g of Example 7 and trimethylolpropane triacrylate of 5.2 g was prepared. obtained in Examples 2 to 5 and 7 the following mixture was prepared the mixture of 100 g (content of fine polymer particles: 5 g) in total

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Using the compositions obtained in Examples 2 to 5 and 7, the following mixture was prepared. That is, the mixture of 100 g (content of fine polymer particles: 5 g) in total, composed of the composition of 7.7 g of Example 2, isobornyl acrylate of 56.35 g, the composition of 5 g of Example 3, tetrahydrofurfuryl acrylate of 0.5 g, the composition of 2 g of Example 4, hydroxyethyl methacrylate of 8 g, the composition of 5 g of Example 5, 1,6-hexanediol diacrylate of 5.25 g, the composition of 5 g of Example 7 and trimethylolpropane triacrylate of 5.2 g was prepared. obtained in Examples 2 to 5 and 7 the following mixture was prepared the mixture of 100 g (content of fine polymer particles: 5 g) in total

Conditions: temp:60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: An aqueous mixture of 751 g deionized water, 101 g Ludox SM-30 (a colloidal silica dispersion, available from E.I. duPont de Nemours & Co.), and 5.5 g of a 50% solution of diethanol-adipic acid condensate (as promoter) was stirred in a glass jar and the mixture was adjusted to a pH of 4 by addition of 10% sulfuric acid. A monomer solution of 88.4 g caprolactone acrylate obtained from Sartomer Co. (Exton, Pa.), 354 g 1,6-hexandiol diacrylate, and 2.1 g VAZO 64 initiator (2,2'-azobis(isobutyronitrile)), available from E.I. duPont de Nemours & Co. was prepared separately. The aqueous mixture and the monomer solution were poured into a 5-liter split resin flask equipped with a marine-propeller type stirrer and mixed at about 1500 rpm (revolutions per minute) for 2 minutes. The mixture was then poured out of the flask and passed through a Manton-Gaulin Homogenizer available from the APV Gaulin Inc. (Everett, Mass.) at 700-900 psi (pounds per square inch, 4.8×106 -6.2×106Pascals) three times. The homogenized suspension was returned to the resin flask. The content was heated with infrared lamps to 60° C. under a nitrogen blanket and agitated at about 500 rpm (revolutions per minute) for 15 hours. A stable suspension of polymer particles was obtained. Analysis with Coulter N4 submicron particle size analyzer, available from Coulter Electronic Inc. (Hinleah, Fla.) showed an average particle size of 1.1 microns. The suspension was filtered with Whatmann #54 filter paper on a 24-cm Buchner funnel and washed several times with deionized water to give a wet cake. The wet cake was placed on glass trays and dried at ambient condition for several days. The dry cake was put in a gallon glass jar along with glass marbles and placed on a roller for several days to give free-flowing powder (average particle size=1.1 microns). An aqueous mixture of 751 g was prepared separately The aqueous mixture and the monomer solution were poured into a 5-liter split resin flask equipped with a marine-propeller type stirrer mixed at about 1500 rpm (revolutions per minute) for 2 minutes The mixture was then poured out of the flask A stable suspension of polymer particles was obtained The suspension was filtered with Whatmann #54 filter paper on a 24-cm Buchner funnel washed several times with deionized water to give a wet cake dried at ambient condition for several days placed on a roller for several days to give free-flowing powder (average particle size=1.1 microns)

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: Using the compositions obtained in Examples 2 to 5 and 7, the following mixture was prepared. That is, the mixture of 100 g (content of fine polymer particles: 5 g) in total, composed of the composition of 7.7 g of Example 2, isobornyl acrylate of 56.35 g, the composition of 5 g of Example 3, tetrahydrofurfuryl acrylate of 0.5 g, the composition of 2 g of Example 4, hydroxyethyl methacrylate of 8 g, the composition of 5 g of Example 5, 1,6-hexanediol diacrylate of 5.25 g, the composition of 5 g of Example 7 and trimethylolpropane triacrylate of 5.2 g was prepared. obtained in Examples 2 to 5 and 7 the following mixture was prepared the mixture of 100 g (content of fine polymer particles: 5 g) in total