Polyether polymer composition
A polymer and composition technology, applied in polyether coatings, conductive coatings, coatings, etc., can solve the problems of insufficient electrical conductivity, thermal conductivity, conductive paste, etc., and achieve excellent long-term stability.
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[0084] Hereinafter, the present invention will be further described based on detailed examples, but the present invention is not limited to these examples. In addition, in the following, "parts" are based on weight unless otherwise specified. In addition, tests and evaluations are as follows.
[0085] (1) Number of repeating units, number-average molecular weight (Mn), and molecular weight distribution (Mw / Mn) of polyether-based polymers
[0086] The number-average molecular weight (Mn) and molecular weight distribution (Mw / Mn) of a polyether-based polymer not containing a cationic group can be obtained as poly The number-average molecular weight (Mn) and molecular weight distribution (Mw / Mn) of the polyether-based polymer were measured using styrene conversion values. In addition, HLC-8320 (manufactured by Tosoh Corporation) was used as a measuring device, a column in which two TSKgelα-M (manufactured by Tosoh Corporation) were connected in series was used as a column, and ...
manufacture example 1
[0104] (Synthesis of polyether polymer A)
[0105] Into a glass reactor with a stirrer replaced with argon, 3.22 g of tetra-n-butylammonium bromide and 100 ml of toluene were added, and the mixture was cooled to 0°C. Next, what dissolved 1.370 g of triethylaluminum (1.2 equivalents with respect to tetra-n-butylammonium bromide) in 10 ml of n-hexane was added, and it was made to react for 15 minutes, and the catalyst composition was obtained. 35.0 g of epichlorohydrin was added to the obtained catalyst composition, and the polymerization reaction was performed at 0 degreeC. After the polymerization reaction is initiated, the viscosity of the solution increases slowly. After reacting for 12 hours, a small amount of water was injected into the polymerization reaction solution to terminate the reaction. The obtained polymerization reaction solution was washed with 0.1N hydrochloric acid aqueous solution to deash the catalyst residue, and after washing with ion-exchanged water, t...
manufacture example 2
[0107] (Synthesis of polyether-based polymer B containing imidazolium structure)
[0108] 5.0 g of the polyether-based polymer A obtained in Production Example 1, 6.1 g of 1-methylimidazole, and 10.0 g of acetonitrile were added to a glass reactor with a stirrer replaced with argon, and heated to 80°C. After reacting at 80° C. for 48 hours, it was cooled to room temperature to terminate the reaction. After washing the obtained reactant with an equal weight mixed solution of toluene / methanol / water, the organic phase containing 1-methylimidazole and toluene was removed, and the aqueous phase was dried under reduced pressure at 50° C. for 12 hours to obtain 6.35 g of light red solid. to the solid 1 H-NMR measurement and elemental analysis, the results identified as: polyether polymer A (polyepichlorohydrin) of the starting material, part of the chlorine group in the repeating unit was 1- with chloride ion as a counter anion A methylimidazolium-containing polymer having a halid...
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