Polyisocyanate composition

A polyisocyanate and isocyanurate technology, applied in the direction of polyurea/polyurethane coatings, coatings, etc., can solve the problems of poor curing and achieve the effect of inhibiting coloration

Active Publication Date: 2014-12-31
ASAHI KASEI KK
View PDF5 Cites 15 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] However, polyisocyanate compositions obtained from 1,6-diisocyanatohexane have inferior curability compared to aromatic polyisocyanate compositions such as MDI (diphenylmethane diisocyanate) and TDI (toluene diisocyanate). this question

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Polyisocyanate composition
  • Polyisocyanate composition
  • Polyisocyanate composition

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0147] Hereinafter, the present invention will be described in more detail based on examples and comparative examples, but the present invention is not limited to the following examples.

[0148]

[0149] The viscosity was measured at 23° C. using an E-type viscometer (manufactured by Tokyo Keiki Co., Ltd.). In the measurement, a standard rotor (1°34'×R24) was used. The rotation speed is as follows.

[0150] 100rpm (less than 128mPa·s)

[0151] 50rpm (over 128mPa·s and less than 256mPa·s)

[0152] 20rpm (over 256mPa·s and less than 640mPa·s)

[0153] 10rpm (over 640mPa·s and less than 1280mPa·s)

[0154] 5rpm (over 1280mPa·s and less than 2560mPa·s)

[0155] In addition, the non-volatile content of the polyisocyanate composition produced in each Example and each comparative example mentioned later was investigated by the method described below, and when the value was 98 mass % or more, it measured it as it was. When it is less than 98% by mass, the concentration of the...

Synthetic example 1

[0250] (Synthesis Example 1: Synthesis of Catalyst)

[0251] Into a 500 mL eggplant-shaped flask replaced with nitrogen, 200 g (0.116 mol) of tetramethylammonium hydroxide (10% by mass methanol solution) (manufactured by Tokyo Chemical Industry Co., Ltd.) was charged at room temperature, and capric acid was added dropwise with a dropping funnel (manufactured by Tokyo Chemical Industry Co., Ltd.) 12.1 g (tetramethylammonium hydroxide / capric acid=1 / 1.1 (molar ratio)), and stirred at room temperature for 30 minutes. Thereafter, methanol was distilled off under conditions of 10 Torr, 50° C., and 30 minutes. 32 g of n-butanol was added thereto to obtain a 50% by mass butanol solution of tetramethylammonium caprate. Then, 40 g of n-butanol was further added to 10 g of the 50 mass % butanol solution of tetramethylammonium caprate, to obtain a 10 mass % butanol solution of tetramethylammonium caprate. Further, 15 g of n-butanol was further added to 10 g of this 10 mass % butanol sol...

Synthetic example 2

[0252] (Synthesis Example 2: Synthesis of Acrylic Polyol)

[0253] Into a four-necked flask equipped with a stirrer, a thermometer, and a condenser, 120.0 g of "SOLVESSO #150" (an aromatic solvent manufactured by Exxon Corporation Chemical Co., Ltd.) and 60.0 g of xylene were charged, and after the inside was replaced with nitrogen, the temperature was raised to 120°C. Thereafter, (meth)acrylic monomers (128.8 g of methyl methacrylate, 84.8 g of n-butyl acrylate, 80.0 g of cyclohexyl methacrylate, 74.4 g of 2-hydroxyethyl methacrylate) were added dropwise over 2 hours. g, styrene 32.0g) and benzoyl peroxide 8.0g, make it carry out stirring reaction. After completion of the dropwise addition, the reaction was further continued at 120° C. for 4 hours to obtain acrylic polyol Ac-1.

[0254] The obtained acrylic polyol Ac-1 had a non-volatile content of 70% by mass, a hydroxyl value of 80 mgKOH / g (value calculated from the feed ratio to the resin component, JIS K1557), and a gla...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
viscosityaaaaaaaaaa
viscosityaaaaaaaaaa
acid valueaaaaaaaaaa
Login to view more

Abstract

The invention provides a polyisocyanate composition which can restrain coloring even adding and storing compounds including tin. The polyisocyanate composition at least employes 1,6-diisocyanato and includes ppm chlorinated compounds with 1-100 mass of chlorine.

Description

technical field [0001] This invention relates to polyisocyanate compositions. Background technique [0002] Polyisocyanate compositions containing an isocyanurate structure obtained from 1,6-diisocyanatohexane (HDI; also called hexamethylene diisocyanate.) are known (for example, Patent Documents 1 to 3). Such a polyisocyanate composition having an isocyanurate structure is widely used. [0003] However, polyisocyanate compositions obtained from 1,6-diisocyanatohexane have inferior curability compared to aromatic polyisocyanate compositions such as MDI (diphenylmethane diisocyanate) and TDI (toluene diisocyanate). this problem. [0004] prior art literature [0005] patent documents [0006] Patent Document 1: Japanese Patent Application Publication No. 45-027982 [0007] Patent Document 2: Japanese Patent Application Laid-Open No. 55-038380 [0008] Patent Document 3: Japanese Patent Laid-Open No. 57-150677 Contents of the invention [0009] The problem to be sol...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C08G18/79C08G18/62C09D175/04
CPCC08G18/792C09D175/04
Inventor 山内理计
Owner ASAHI KASEI KK
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products