Direct-to-plate flexographic printing plate precursor

Details Direct-to-plate flexographic printing plate precursor Direct-to-plate flexographic printing plate precursor

2001-03-16

2003-04-22

Hamilton, Cynthia (Department: 1752)

Radiation imagery chemistry: process, composition, or product th

Imaging affecting physical property of radiation sensitive...

Radiation sensitive composition or product or process of making

C430S005000, C430S306000, C430S309000

Reexamination Certificate

active

06551759

ABSTRACT:

DESCRIPTION
1. Field of the Invention
The present invention relates to a direct-to-plate flexographic printing plate precursor, more specifically to a flexographic printing plate precursor that can be developed thermally without the use of aqueous or organic processing solutions.
Furthermore the present invention relates to a method for making a direct-to-plate flexographic printing plate.
2. Background of the Invention
Flexographic printing plates are used for printing on soft and deformable surfaces such as plastic films, cardboard etc. Flexographic printing plate precursors typically contain a photopolymerizable layer comprising an elastomeric binder, a monomer and a photoinitiator. Conventionally, a photosensitive negative or positive of the desired image is used as a contact mask for the flood exposure of the photopolymerizable layer. In computer-to-plate technology, the conventional contact mask is replaced by a mask that is integrated within the printing plate precursor. Such an integrated mask can be provided by printing with an ink jet printer on the photopolymeric plate or by providing the polymeric plate with an ablatable image-recording layer that is substantially opaque to actinic radiation. This material may be called a direct-to-plate flexographic printing plate precursor.
Direct-to-plate flexographic printing plate precursors have been described in e.g. EP-A n° 99113770.4, WO-A-96 16356, EP-A-767 407, WO-A-94 03838 and WO-A-94 03839. These patents describe flexographic printing plate precursors comprising on a support a photopolymerizable layer and an IR-sensitive image-recording layer. Flexographic printing plates are produced by image-wise laser exposure inducing ablative removal to form a mask, UV flood exposure through the mask and development with an aqueous or organic solution. Such developing steps are time consuming and therefor expensive. In addition, potentially toxic waste products are produced.
In EP-A-468 745, EP-A-468 667 and U.S. Pat. No. 5,215,859 conventional flexographic printing plate precursors are described comprising photopolymerizable polyurethane resins that can be developed thermally without requiring the use of aqueous or organic developing solutions as described in EP-A-469 735. This patent discloses a device to produce flexographic printing plates wherein the image-wise exposed photopolymerizable layer of the flexographic printing plate precursor is heated for a time and to a temperature sufficient to cause the unexposed areas to liquefy. Then the photopolymerizable layer is contacted with an absorbent material at a pressure sufficient for a portion of the liquefied areas to be absorbed. This step is repeated several times to clean up the unexposed areas.
However, when the above described prior art direct-to-plate flexographic printing plate precursors are applied in such a device problems arise since the integrated mask can not be thermally liquefied sufficiently. This prevents the removal of the integrated mask together with the unexposed, liquefied areas of the photopolymerizable layer.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a material for making a direct-to-plate flexographic printing plate precursor that can be developed without the use of aqueous or organic processing solutions.
It is a further object of the present invention to provide a method for making a direct-to-plate flexographic printing plate precursor.
The above mentioned objects are realized by the material and the method as defined by the independent claims.
A material for making a direct-to-plate flexographic printing plate precursor that can be developed thermally without the use of aqueous or organic processing solutions is obtained by providing an image recording layer and a photopolymerizable layer that each can be liquefied so that they can be penetrated to a depth of at least 5% at a temperature of 110° C. by a ballpoint probe having a diameter of 3 mm, which is subjected to a force of 0.1N. Upon imaging and flood exposure the image-recording layer and the photopolymerizable layer are liquefied by heating. Thereafter the image-recording layer is removed together with the unexposed areas of the photopolymerizable layer by using an absorbent material.
DETAILED DESCRIPTION OF THE INVENTION
It has been found that, according to the present invention, a direct-to-plate flexographic printing plate precursor can be obtained that can be developed thermally without the use of aqueous or organic processing solutions. Hereto a thermoplastic binder with a glass transition temperature preferably below 65° C. is incorporated in the image recording layer and the photopolymerizable layer so that each can be penetrated to a depth of at least 5% at a temperature of 110° C. by a ballpoint probe. Penetration depths were measured with a Mettler TMA40 thermo mechanical analyzer. Thereto a 100 &mgr;m thick image recording layer or photopolymerizable layer was coated on a glass support and dried. A quartz ballpoint probe having a diameter of 3 mm was positioned on the surface of the image recording layer or photopolymerizable layer. A force of 0.1 N was applied onto the ballpoint probe while heating the material and the probe in an oven from 30° C. to 160° C. at a speed of 10° C./min. The penetration depth (%) is determined as follows at a temperature of 110°:
Relative penetration depth=[absolute depth (&mgr;m)/absolute thickness of the image recording layer (&mgr;m)]×100
Preferred thermoplastic binders for use in the image recording layer are polyesters, poly(meth)acrylates, polyvinylacetates or copolymers thereof or elastomeric polyurethane resins. Suitable commercially available binders are Dynapol S1404 (from Huls A. G.), Carboset 525 (from Goodrich), Mowilith CT5 (from Hoechst), Vitel VPE5545 (from Goodyear) and Vinnapas B100 (from Wacker Chemie).
According to the present invention the image recording layer is preferably a laser ablatable layer that further comprises a light absorbing compound. Preferred light absorbing compounds are IR-absorbing dyes such as phthalocyanines or derivatives, cyanine dyes, merocyanine dyes and polymethine dyes or inorganic pigments such as carbon black, graphite, iron oxide or chromium oxide. Preferably carbon black is used. Furthermore carbon black renders the ablatable layer opaque to UV radiation, so there is no need to add an additional UV-absorbing dye. It is particularly preferred to use fine-grained carbon black with a mean particle size below 30 nm which is commercially available as Printex® U, Printex® L6, Specialschwarz 4 or Specialschwarz 250 (all trademarks from Degussa).
Suitable supports for the imaging material of the present invention are flexible but dimensionally stable materials such as films of polyethylene therephthalate, cellulose triacetate, polyethylene naphthalate, polybutylene terephthalate or polycarbonate that have a sufficiently high modulus. Also metal supports can be used.
A photopolymerizable layer containing an elastomeric binder is provided onto the support. A preferred elastomeric binder is a photopolymerizable polyurethane resin derived from polymer forming reactions of (a) 10-50% by weight of at least one diisocyanate, (b) 0.5-20% by weight of a first chain extension agent having at least two free hydrogen groups and having at least one ethylenically unsaturated addition polymerizable group per molecule (optionally, a second chain extension agent may be present having at least two free hydrogen groups (0.5-20% by weight)) and (c) 10-70% by weight of an organic polyol having a molecular weight of at least 500 and containing at least two free hydrogen groups per molecule. The polyurethane resins used in the present invention have a molecular weight of at least 10.000 and a glass transition temperature of less than 65° C. The polyurethane resins belong to a class of polymers known as segmented copolymers or multiphase polymers. The elastomeric properties of these polymers result from phase separation between so called ‘hard’ segment domains and ‘soft’ s

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