IP Library Granted Patent US 7,084,183
Granted Patent B2
US 7,084,183 · App. 10/494,593 · Granted Aug 1, 2006

Difunctional photoinitiators

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Quick Facts
Patent No.
US 7,084,183
App. No.
10/494,593
Granted
Aug 1, 2006
Kind
B2
Abstract

The invention relates to α-hydroxy ketones of formula I or IIa; or mixtures of compounds of formula I and II; or mixtures of compounds of formulae Ia and IIa

Claims (31)

1. A crystalline isomeric mixture of α-hydroxy ketone compounds of formulae Ia and IIa

where the water content is from 2 to 8% by weight.

2. An isomeric mixture according to claim 1 , having a content of para-para compound of from 99.9 to 25% by weight and having a content of meta-para compound of from 0.1 to 75% by weight.

3. A process for the preparation of a crystalline isomeric mixture of compounds of formulae Ia and IIa according to claim 1 ,

which process comprises reacting diphenylmethane with isobutyric acid halide in the presence of a Friedel-Crafts catalyst, and chlorinating and hydrolysing the resulting isomeric mixture consisting of bis[4-(2-methyl-propionyl)-phenyl]-methane and [3-(2-methyl-propionyl)-phenyl]-[4-(2-methyl-propionyl)-phenyl]methane, hydrolysis of the isomeric mixture yielding an aqueous phase and an organic phase that comprises the hydrolysis product; wherein further processing of the hydrolysis product comprises the following steps

a) addition of from 3 to 20% by weight of water to the organic phase, crystallisation and isolation of the water containing isomeric mixture of formulae Ia and IIa and

b) where appropriate, drying of the isomeric mixture obtained in step a) to remove excess water and obtain a crystalline isomeric mixture.

4. A composition comprising

(A) at least one ethylenically unsaturated compound,

(B) an isomeric mixture of compounds of formulae Ia and IIa according to claim 1 ,

(C) optionally a film-forming binder based on a thermoplastic or thermocurable resin;

(D) optionally, further additives,

(E) optionally, further photoinitiators and coinitiators.

5. A process for the production of a scratch-resistant durable surface, wherein

(1) a composition according to claim 4 is prepared;

(2) the formulation is applied to a support; and

(3) curing of the formulation is carried out either only by means of irradiation with electromagnetic radiation having a wavelength of from 200 nm to within the IR range, or by irradiation with electromagnetic radiation and prior, simultaneous and/or subsequent action of heat.

6. A process according to claim 5 for the production of pigmented and non-pigmented surface coatings, overprint coatings, powder coatings, printing inks, gel coats, composite materials or glass fibre coatings.

7. A coated substrate which is coated on at least one surface with a cured composition according to claim 4 .

8. A composition comprising

(A) an ethylenically unsaturated compound containing at least one aminoacrylate,

(B) an isomeric mixture of compounds of formulae Ia and IIa according to claim 1 ,

(C) optionally a film-forming binder based on a thermoplastic or thermocurable resin;

(D) optionally, further additives,

(E) optionally, further photoinitiators and coinitiators.

9. A process for the production of a scratch-resistant durable surface, wherein

(1) a composition according to claim 8 is prepared;

(2) the formulation is applied to a support; and

(3) curing of the formulation is carried out either only by means of irradiation with electromagnetic radiation having a wavelength of from 200 nm to within the IR range, or by irradiation with electromagnetic radiation and prior, simultaneous and/or subsequent action of heat.

10. A process according to claim 9 for the production of pigmented and non-pigmented surface coatings, overprint coatings, powder coatings, printing inks, gel coats, composite materials or glass fibre coatings.

11. A coated substrate which is coated on at least one surface with a cured composition according to claim 8 .

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2020
From: BASF SE
To: IGM GROUP B.V.
Reel/Frame 052450/0001 →
CHANGE OF NAME Recorded Apr 20, 2020
From: CIBA SPECIALTY CHEMICALS CORPORATION
To: CIBA CORPORATION
Reel/Frame 052444/0657 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2020
From: CIBA CORPORATION
To: BASF SE
Reel/Frame 052446/0891 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2004
From: FUCHS, ANDRE; HUSLER, RINALDO; SCHREGENBERGER, CHRISTIAN; KUNZ, MARTIN
To: CIBA SPECIALTY CHEMICALS CORP.
Reel/Frame 015857/0735 →