Sealing agent for organic electroluminescence display device
A technology for electroluminescence display and display components, which is applied in the direction of electroluminescence light sources, electrical components, electric light sources, etc., can solve problems such as degradation and reduction of luminous characteristics, and achieve the effect of excellent wettability and good efficiency
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Embodiment 1
[0230] 100 parts by mass of trifluoromethyl methacrylate (manufactured by Tokyo Chemical Industry Co., Ltd.) and 5 parts by mass of 2,4,6-trimethylbenzoyldiphenylphosphine oxide (TPO) (manufactured by BASF Japan Co., Ltd.) were mixed , to prepare the sealant. In addition, content of a fluorine atom with respect to the total amount of a monomer component was 32 mass %. The obtained sealing compound was evaluated by the evaluation method shown below. In addition, the obtained sealing compound was cured under the photocuring conditions shown below to form a cured body, and the water vapor transmission rate of the cured body was evaluated by the method shown below.
[0231] [Surface Tension]
[0232] The static surface tension of the sealant was measured by the pendant drop method in an atmosphere of 23° C. using (DM500 manufactured by Kyowa Interface Science Co., Ltd.). The measurement results are shown in Table 1.
[0233] [wettability]
[0234] On a 70 mm x 70 mm x 0.7 mmt...
Embodiment 2
[0244] Except for using 100 parts by mass of pentafluorobenzyl methacrylate (manufactured by Tokyo Chemical Industry Co., Ltd.) instead of trifluoromethyl methacrylate, it was carried out in the same manner as in Example 1, and a sealant and its cured body were produced and evaluated. . Table 1 shows the evaluation results. In addition, content of a fluorine atom with respect to the total amount of a monomer component was 34 mass %.
Embodiment 3
[0246] A sealant was produced in the same manner as in Example 1 except that 100 parts by mass of 2,2,3,3-tetrafluoropropyl acrylate (manufactured by Osaka Organic Chemical Industry Co., Ltd.) was used instead of trifluoromethyl methacrylate. and its cured body and evaluated. Table 1 shows the evaluation results. In addition, content of a fluorine atom with respect to the total amount of a monomer component was 39 mass %.
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