Stereolithography resin compositions and three-dimensional objects made therefrom
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examples 2 to 5
[0193]Curable liquid resin compositions were prepared in the same manner as in Example 1, except for using the compounds shown in Table 3 as component (F). Test specimens (cured products) were prepared from the resulting liquid resin compositions for evaluation. The evaluation method is the same as described above. The results are shown in Table 3.
TABLE 3Example 2Example 3Example 4Example 5Type of componentPB / GMA +PB / GMA +PB / alicyclicPB / OXMA +(F) (core / shell layer)PMMAPMMAepoxy + PMMAPMMAContent of2,4101,8102,4901,900functional group(g / eq)Diameter of100100100100component (F) (nm)Viscosity (mPa · s)1,2001,2101,2101,200[Evaluation]Bending modulus of2,1002,0002,1002,200elasticity (MPa)Izod impact value2.43.73.54.3(kJ / m2)PB: PolybutadieneGMA: Glycidyl methacrylate (monomer for epoxy modification)PMMA: Polymethyl methacrylateAlicyclic epoxy: Methacrylate having an alicyclic epoxy group (monomer for epoxy modification), “CYCLOMER M100” manufactured by Daicel Chemical Industries, Ltd.OXMA:...
example 6
[0194]The same experiment as in Example 2 was carried out except that the test specimen (cured product) was heated at 80° C. for two hours after molding.
example 7
[0195]The same experiment as in Example 3 was carried out except that the test specimen (cured product) was heated at 80° C. for two hours after molding.
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