Isocyanate composition, method for producing isocyanate polymer and isocyanate polymer

Patent metadata

Field	Value
Publication number	US-11174337-B2
Application number	US-201716340633-A
Country	US
Kind code	B2
Filing date	Oct 13, 2017
Priority date	Oct 14, 2016
Publication date	Nov 16, 2021
Grant date	Nov 16, 2021

Abstract

The present invention provides an isocyanate composition including an isocyanate compound having an ethylenically unsaturated bond, a compound represented by formula (1) (in the formula, R1 represents an a-valent organic group, R2 represents a monovalent organic group, a represents an integer of 1 or 2), and/or a compound having a UV absorption in a spectral region of a decamer or higher isocyanate measured by gel permeation chromatography; and an isocyanate composition including an isocyanate compound having an ethylenically unsaturated bond, or a compound having at least one unsaturated bond other than an unsaturated bond constituting an aromatic ring or an inert compound such as a hydrocarbon compound or the like and having a carbon-carbon unsaturated bond other than an unsaturated bond constituting an aromatic ring; or the likeR1—(COO—R2)a  (1).

First claim

The invention claimed is:

1. An isocyanate composition, comprising
an isocyanate compound having an ethylenically unsaturated bond; and
1.0 to 1.0×10 4 ppm by mass of a compound represented by the following formula (1) which is different from the isocyanate compound with respect to a total mass of the isocyanate compound, and/or
1.0 to 1.0×10 4 ppm by mass of a compound having a UV absorption in a spectral region of a decamer or higher isocyanate measured by gel permeation chromatography with respect to a total mass of the isocyanate compound, and/or
1.0 to 1.0×10 4 ppm by mass of a compound having an isocyanurate group and/or a biuret group with respect to a total mass of the isocyanate compound,
R 1 —(COO—R 2 ) a   (1)

(in the formula, R 1 represents an a-valent aliphatic group having 2 to 10 carbon atoms or aromatic group having 6 to 10 carbon atoms, R 2 represents a monovalent aliphatic group having 2 to 10 carbon atoms or aromatic group having 6 to 25 carbon atoms, and a represents an integer of 1 or 2).

2. The isocyanate composition according to claim 1 , wherein the isocyanate composition further comprises, with respect to a total mass of the isocyanate compound,
1.0 to 2.0×10 4 ppm by mass of at least one inert compound selected from the group consisting of a hydrocarbon compound, an ether compound, a sulfide compound, a halogenated hydrocarbon compound, a silicon-containing hydrocarbon compound, a silicon-containing ether compound and a silicon-containing sulfide compound, the inert compound not having a carbon-carbon unsaturated bond and a carbon-oxygen double bond other than an unsaturated bond constituting an aromatic ring.

3. The isocyanate composition according to claim 1 , wherein the isocyanate composition further comprises 1.0 to 2.0×10 4 ppm by mass of a carbonic acid derivative with respect to a total mass of the isocyanate compound.

4. The isocyanate composition according to claim 1 , wherein the isocyanate composition further comprises, with respect to a total mass of the isocyanate compound,
1.0 to 1.0×10 2 ppm by mass of a sulfuric acid and/or a sulfuric ester, and/or
1.0 to 1.0×10 2 ppm by mass of a phosphoric acid and/or a phosphoric ester.

5. The isocyanate composition according to claim 1 , wherein the isocyanate composition further comprises, with respect to a total mass of the isocyanate compound,
1.0 to 1.0×10 4 ppm by mass of a basic amino compound, and/or a halogen ion, and/or a hydrolysable halogen compound.

6. An isocyanate composition, comprising
an isocyanate compound having an ethylenically unsaturated bond; and
with respect to a total mass of the isocyanate compound, 1.0 to 1.0×10 4 ppm by mass of a compound different from the isocyanate compound and having at least one unsaturated bond other than an unsaturated bond constituting an aromatic ring, or
with respect to a total mass of the isocyanate compound, 1.0 to 2.0×10 4 ppm by mass of an inert compound not having a carbon-carbon unsaturated bond other than an unsaturated bond constituting an aromatic ring, which is at least one selected from the group consisting of a hydrocarbon compound, an ether compound, a sulfide compound, a halogenated hydrocarbon compound, a silicon-containing hydrocarbon compound, a silicon-containing ether compound and a silicon-containing sulfide compound with respect to a total mass of the isocyanate compound, and/or 1.0 to 1.0×10 2 ppm by mass of a sulfuric acid and/or a sulfuric ester, and/or 1.0 to 1.0×10 2 ppm by mass of a phosphoric acid, and/or a phosphoric ester,
wherein the compound different from the isocyanate compound and having at least one unsaturated bond other than an unsaturated bond constituting an aromatic ring is at least one selected from the group consisting of the compounds represented by formulas (5), (6), (7) and (2),

in which each of R 9 , R 10 , R 11 and R 12 independently represents an aliphatic group having 1 to 20 carbon atoms, an aliphatic group having 7 to 20 carbon atoms and substituted with an aromatic compound, an aromatic group having 6 to 20 carbon atoms or a hydrogen atom, a total number of carbon atoms constituting R 9 and R 11 is an integer of 0 to 20, and a total number of carbon atoms constituting R 10 and R 12 is an integer of 0 to 20,

in which R 13 represents an aliphatic group having 1 to 20 carbon atoms, an aliphatic group having 7 to 20 carbon atoms and substituted with an aromatic group, or an aromatic group having 6 to 20 carbon atoms.

in which each of R 14 and R 15 independently represents an aliphatic group having 1 to 20 carbon atoms, an aliphatic group having 7 to 20 carbon atoms and substituted with an aromatic group, an aromatic group having 6 to 20 carbon atoms,

in which R 3 represents a residue obtained by removing an isocyanate group from an isocyanate compound having an ethylenically unsaturated bond, and R 4 represents an organic group.

7. The isocyanate composition according to claim 6 , including
the isocyanate compound; and
the compound different from the isocyanate compound and having at least one unsaturated bond other than an unsaturated bond constituting an aromatic ring.

8. The isocyanate composition according to claim 6 , wherein
the carbonic acid derivative is at least one compound selected from the group consisting of a carbonic acid ester, N-unsubstituted carbamic acid ester, and N-substituted carbamic acid ester.

9. The isocyanate composition according to claim 8 , wherein
the N-substituted carbamic acid ester is a compound represented by the following formula (2)

[in formula (2), R 3 represents an isocyanate group-removed residue of the isocyanate compound, and R 4 represents an organic group].

10. The isocyanate composition according to claim 6 , including the isocyanate compound and the inert compound.

11. The isocyanate composition according to claim 6 , including the isocyanate compound, the compound different from the isocyanate compound and having at least one unsaturated bond other than an unsaturated bond constituting an aromatic ring, and the inert compound.

12. The isocyanate composition according to claim 11 , including the isocyanate compound, and the compound different from the isocyanate compound and having at least one unsaturated bond other than an unsaturated bond constituting an aromatic ring, wherein
the unsaturated bond other than an unsaturated bond constituting an aromatic ring is a double bond between carbon and oxygen.

13. The isocyanate composition according to claim 12 , wherein
the compound having at least one unsaturated bond other than an unsaturated bond constituting an aromatic ring is a carbonic acid derivative.

14. The isocyanate composition according to claim 13 , wherein
the carbonic acid derivative is at least one compound selected from the group consisting of a carbonic acid ester, an N-unsubstituted carbamic acid ester, and an N-substituted carbamic acid ester.

15. The isocyanate composition according to claim 1 , wherein
97% by mass or more of the isocyanate compound is included with res

Assignees

• Asahi Chemical Ind

Inventors

• Miyake Nobuhisa
• Shinohata Masaaki
• Ohkubo Atsushi
• Nakaoka Koichi
• Kosugi Yuji

Classifications

• C08G18/8116 Primary

  esters of acrylic or alkylacrylic acid having only one isocyanate or isothiocyanate group · CPC title

• C08K5/01

  Hydrocarbons {(C08K5/0091 takes precedence)} · CPC title

• C08G18/092

  oligomerisation to isocyanurate groups · CPC title

• C08G18/73

  acyclic · CPC title

• C08K5/205

  Compounds containing [IMAGE cpc-sch-C08K-1010.gif] groups, e.g. carbamates · CPC title