Method for producing metal powder-containing composition
A metal powder, manufacturing method technology, applied in metal processing equipment, overvoltage arresters using spark gaps, nanotechnology for materials and surface science, etc. Settling, composition curing and other problems, to achieve the effect of suppressing poor dispersion and excellent stability over time
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[0114] Hereinafter, the present invention will be more specifically described based on examples, but the present invention is not limited to these examples at all.
[0115] The properties of the metal powder-containing compositions obtained in Examples and Comparative Examples were evaluated as follows.
[0116]
[0117] About 50 g of the metal powder-containing composition was put into an airtight container, and the state of the composition after leaving it to stand for 2 days or more in a thermostat set at 50° C. was confirmed with a medicine spoon. Stability over time was evaluated by the following criteria.
[0118] (benchmark)
[0119] A: Not cured.
[0120] B: A small amount of curing was observed at the bottom.
[0121] C: Overall curing.
[0122]
[0123] About 50 g of the metal powder-containing composition was put into an airtight container, and the state of the composition after leaving it to stand for 12 hours or more in a thermostat set at 50° C. was check...
Synthetic example 1
[0130]In a reaction vessel equipped with a stirring device, a thermometer, and a condenser, C-1015N (polycarbonate diol manufactured by Kuraray Co., Ltd., raw material diol molar ratio: 1,9-nonanediol: 2-methyl-1,8-octanediol=15:85, molecular weight: 964) 718.2 g, 2,2-dimethylol butyric acid (manufactured by Nippon Chemical Co., Ltd.), which is a dihydroxy compound having a carboxyl group, 136.6 g. 1293 g of diethylene glycol ethyl ether acetate (manufactured by Daicel Chemical Co., Ltd.) as a solvent, and all the raw materials were dissolved at 90°C.
[0131] The temperature of the liquid in which the raw material was dissolved was lowered to 70° C., and methylene bis(4-cyclohexyl isocyanate) (manufactured by Sumika Bayer Uretan Co., Ltd., trade name "デスモジュール-W") 237.5g.
[0132] After completion of the dropwise addition, the reaction was carried out at 80°C for 1 hour, at 90°C for 1 hour, and at 100°C for 1.5 hours. After confirming that the isocyanate had almost disappeare...
Synthetic example 2
[0135] In a 5-liter four-necked flask equipped with a stirrer, a cooling tube with an oil-water separator, a nitrogen introduction tube, and a thermometer, PLACCEL CD-220 (1,6-hexanediol-based polycarbonate produced by Daicel Chemical Co., Ltd. 1000.0 g (0.50 mol) of ester diol), 250.27 g (1.00 mol) of 4,4'-diphenylmethane diisocyanate, and 833.51 g of γ-butyrolactone were heated up to 140°C. It reacted at 140 degreeC for 5 hours, and obtained the 2nd diisocyanate. 288.20 g (1.50 mol) of trimellitic anhydride, 125.14 g (0.50 mol) of 4,4′-diphenylmethane diisocyanate and 1361.14 g of γ-butyrolactone, which are polycarboxylic acids having acid anhydride groups, were charged in the reaction liquid, After raising the temperature to 160° C., it was reacted for 6 hours to obtain an acid anhydride group-containing thermosetting polyurethane resin having a number average molecular weight of 18,000 (hereinafter referred to as “thermosetting polyurethane resin 2”). The obtained thermos...
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