Electrically conductive material and method for producing same
A technology of conductive materials and manufacturing methods, applied in metal material coating process, coating, liquid chemical plating, etc., can solve problems such as can not be called a sufficient solution, poor electroplating, and non-uniformity of plating
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[0115] The following examples are given to illustrate the present invention in more detail, but the present invention is not limited to these examples. In addition, unless otherwise specified, "%" means "mass %".
[0116] The equipment used in the present invention is as follows.
[0117] 1 H-NMR: manufactured by JEOL Ltd., AL300, 300Hz
[0118] TEM observation: manufactured by JEOL Ltd., JEM-2200FS
[0119] SEM observation: Super-resolution field emission scanning electron microscope S-800 manufactured by Hitachi, or VE-9800 manufactured by KEYENCE CORPORATION
[0120] TGA measurement: manufactured by SII NanoTechnology Inc., TG / DTA6300
[0121] Plasma absorption spectrum: manufactured by Hitachi, Ltd., UV-3500
[0122] Dynamic light scattering particle size measuring device: FPAR-1000 manufactured by Otsuka Electronics Co., Ltd.
[0123] Surface resistance value measurement: manufactured by Mitsubishi Chemical Corporation, low resistivity meter Loresta EP (4-terminal m...
Synthetic example 1
[0128] Synthesis Example 1 [Synthesis of compound (P1-1) having polyethylene glycol (PEG)-branched polyethyleneimine (PEI) structure]
[0129] 1-1[Synthesis of Tosylated Polyethylene Glycol]
[0130] Prepared by mixing 150 g (30 mmol) of single-terminal methoxylated polyethylene glycol (hereinafter referred to as PEGM) [number average molecular weight (Mn) 5000] (manufactured by Aldrich) and 24 g (300 mmol) of pyridine in 150 ml of chloroform, respectively. solution, and a solution obtained by uniformly mixing 29 g (150 mmol) of toluenesulfonyl chloride and 30 ml of chloroform.
[0131] While stirring the mixed solution of PEGM and pyridine at 20°C, a toluene solution of toluenesulfonyl chloride was added dropwise thereto. After completion of the dropwise addition, it was reacted at 40° C. for 2 hours. After completion of the reaction, 150 ml of chloroform was added for dilution, and after washing with 250 ml (340 mmol) of 5% aqueous HCl solution, it was washed with saturate...
Synthetic example 2
[0134] Synthesis Example 2 [Synthesis of Compound (P1-2) Having PEG-Branched PEI-Bisphenol A Type Epoxy Resin Structure]
[0135] 2-1 [Modification of epoxy resin]
[0136] After dissolving 37.4 g (20 mmol) of bisphenol A type epoxy resin EPICLON AM-040-P (manufactured by DIC Corporation) and 2.72 g (16 mmol) of 4-phenylphenol in 100 ml of DMA, add 65% ethyl triphenyl acetate 0.52 ml of phosphonium ethanol solution was reacted at 120° C. for 6 hours under a nitrogen atmosphere. After standing to cool, it was added dropwise to a large amount of water, and the obtained precipitate was further washed with a large amount of water. The reprecipitated purified product was filtered and then dried under reduced pressure to obtain a modified bisphenol A epoxy resin. The yield of the product obtained was 100%.
[0137] conduct 1 H-NMR measurement was used to examine the integral ratio of epoxy groups. As a result, 0.95 epoxy rings remained in 1 molecule of bisphenol A epoxy resin, a...
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