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Modified polyaspartic acid ester and curable resin composition

A technology of polyaspartic acid ester and curable resin, which is applied in the direction of polyurea/polyurethane adhesive, polyurea/polyurethane coating, adhesive type, etc. It can solve the problem that the cured product is easy to break, has not been found, and reduces brittleness and other issues, to achieve the effect of excellent toughness and appearance

Active Publication Date: 2017-08-18
KANEKA CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the cured product (polyurea resin) obtained from polyaspartic acid ester has the problem of being brittle and easily broken
In addition, there is also a demand in the market to reduce brittleness, that is, to improve toughness, but currently, an effective method for improving toughness without greatly affecting other physical properties (such as appearance) has not been found.

Method used

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  • Modified polyaspartic acid ester and curable resin composition
  • Modified polyaspartic acid ester and curable resin composition
  • Modified polyaspartic acid ester and curable resin composition

Examples

Experimental program
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Embodiment

[0222] Hereinafter, the present invention will be described in more detail through examples and comparative examples, but the present invention is not limited to them, and appropriate changes can be implemented within the range that can be adapted to the above-mentioned and following gist, and they are all included in the technical scope of the present invention. Inside. In addition, "part" and "%" in a following Example and a comparative example mean a weight part or weight%.

[0223] In addition, the measurement and test in the following manufacture example, an Example, and a comparative example were performed as follows.

[0224] [1] Measurement of average particle diameter of polymer particles

[0225] The volume average particle diameter (Mv) of the polymer particle dispersed in the aqueous latex was measured using Microtrac UPA150 (made by Nikkiso Co., Ltd.). As a measurement sample, polymer particles diluted with deionized water were used.

[0226] [2] Measurement of...

manufacture example 1-1

[0264] Production Example 1-1: Preparation of Polybutadiene Rubber Latex (R-1)

[0265] Put 200 parts of deionized water, 0.03 parts of tripotassium phosphate, 0.25 parts of potassium dihydrogen phosphate, 0.002 parts of disodium ethylenediaminetetraacetic acid (EDTA), 0.001 parts of ferrous sulfate into the pressure-resistant polymerizer. Heptahydrate salt (Fe) and 0.15 parts of sodium dodecylbenzenesulfonate (SDS), while stirring, fully carry out nitrogen replacement and remove oxygen, then drop 100 parts of butadiene (BD) into the system, and heat up to 45°C. Putting in 0.015 pairs of Alkane hydroperoxide (PHP), followed by adding 0.04 parts of sodium formaldehyde sulfoxylate (SFS), to start polymerization. At 4 hours from the start of the polymerization, 0.3 part of SDS, 0.01 part of PHP, 0.0015 part of EDTA and 0.001 part of Fe were charged. Furthermore, 0.4 part of SDS was injected|thrown-in at the 7th hour from the start of polymerization. At the 10th hour of the p...

manufacture example 1-2

[0266] Production Example 1-2: Preparation of Organosiloxane Rubber Latex (R-2)

[0267]251 parts of deionized water, 1.8 parts of dodecylbenzenesulfonic acid, 100 parts of octamethylcyclotetrasiloxane, 2 parts of tetraethoxysilane, 2 parts of γ-acryloyloxypropane The mixed solution of oxydimethoxymethylsilane was stirred at 10000 rpm for 5 minutes with a homomixer to prepare latex. This latex was passed twice through a high-pressure homogenizer set at a pressure of 30 MPa. The obtained latex was stirred, and put all at once into a 5-port glass container equipped with a reflux cooler, a nitrogen blowing port, an additional port for monomers and emulsifiers, and a thermometer. The system was heated up to 80° C. over about 40 minutes while stirring, and then reacted at 80° C. for 6 hours. Thereafter, after cooling to 25° C. and leaving for 20 hours, the pH of the system was returned to 6.8 with sodium hydroxide to terminate the polymerization, and a latex containing organosilo...

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Abstract

The present invention pertains to: a modified polyaspartic acid ester which includes polyaspartic acid ester (A) and polymer microparticles (B) having a volume-average particle diameter of 0.01-0.6 [mu]m, wherein the content of the polymer microparticles (B) is 0.5-70 wt%; and a curable resin composition which includes polyaspartic acid ester (A), polymer microparticles (B), and polyisocyanate (C), wherein the volume-average particle diameter of the polymer microparticles is 0.01-0.6 [mu]m.

Description

technical field [0001] The present invention relates to a modified polyaspartic ester and a curable resin composition suitable for coatings, castings, composite materials, etc. having excellent toughness and appearance. Background technique [0002] In recent years, polyurea coatings composed of polyamines and polyisocyanates have been widely used due to their rapid reactivity, excellent mechanical properties of cured products, chemical resistance, and the like. Among them, polyurea coatings using polyaspartic acid ester as a polyamine have attracted attention due to their moderate curing speed and the ability to thicken the coating film (such as non-patent document 1), and their usage in the market has also been increasing. Increase. In addition, polyurea resins obtained from polyaspartic esters are attracting attention for applications other than coatings because of their good mechanical properties. However, cured products (polyurea resins) obtained from polyaspartic aci...

Claims

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Application Information

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IPC IPC(8): C08L75/04C08G18/60C08L51/00C09D175/04C09J175/04
CPCC09D175/04C09J175/04C08L51/00C08L75/04C08F265/06C08F279/02C08F283/124C08L51/04C08L51/08C08L2207/53C08G18/60C08F230/085C08F212/08C08F220/14C08F220/20C08L77/04C08F220/1804C08F220/1808C08F220/40C08L51/003
Inventor 宫武信雄
Owner KANEKA CORP