Pressure-sensitive adhesives for bonding flexible printing plates

Patent metadata

Field	Value
Publication number	US-10072188-B2
Application number	US-201715647893-A
Country	US
Kind code	B2
Filing date	Jul 12, 2017
Priority date	Jul 19, 2016
Publication date	Sep 11, 2018
Grant date	Sep 11, 2018

Abstract

A pressure-sensitive adhesive comprising at least one adhesive component comprising at least one polymer component based on a monomer mixture comprising at least one of the following monomers:
at least one acrylic ester at least one methacrylic ester acrylic acid methacrylic acid

is particularly suitable for the bonding of printing plates, particularly to printing cylinders and/or printing sleeves, if the pressure-sensitive adhesive further comprises 1 to 25 wt %, preferably 2 to 20 wt %, based in each case on the overall blend of the at least one adhesive component without solvent, of at least one compound selected from the group consisting of stearyl alcohol, aliphatic and aromatic dicarboxylic esters, acetylated polyols and ethoxylated fatty acid amines.

First claim

The invention claimed is:

1. Method for the bonding of printing plates to printing cylinders and/or printing sleeves with a pressure-sensitive adhesive comprising at least one adhesive component comprising at least one polymer component based on a monomer mixture comprising at least one of the following monomers:
at least one acrylic ester
at least one methacrylic ester
acrylic acid
methacrylic acid

wherein the pressure-sensitive adhesive further comprises
1 to 25 wt %, based on the overall blend of the at least one adhesive component without solvent, of at least one compound selected from the group consisting of stearyl alcohol, aliphatic dicarboxylic esters, acetylated polyols and ethoxylated fatty acid amines.

2. Method according to claim 1 , wherein the at least one compound is selected from the group consisting of polyethylene(15)cocosamine, ethoxylated(15)N-tallow-1,3-diaminopropane, oleylamine oxethylate, benzyl-2-ethylhexyl adipate, di-n-butyl adipate, di-2-ethylhexyl adipate, glycerol acetate, dibutyl sebacate and di-(2-ethylhexyl)-sebacate.

3. Method according to claim 1 , wherein the at least one compound is stearyl alcohol and is present in an amount of 1 to 15 wt %, based on the overall blend of the at least one adhesive component without solvent.

4. Method according to claim 1 , wherein the monomer mixture comprises at least the following monomers:
a) 20 to 99.5 wt % of at least one acrylic ester and/or methacrylic ester whose homopolymer has a static glass transition temperature of <0° C.;
b) 0 to 40 wt % of at least one acrylic ester and/or methacrylic ester whose homopolymer has a static glass transition temperature of >0° C.;
c) 0.5 to 20 wt % of acrylic acid and/or methacrylic acid;
d) 0 to 25 wt % of further copolymerizable monomers, the quantity figures being based in each case on the monomer mixture.

5. Method according to claim 4 , wherein the polymer component or polymer components based on monomer mixtures comprising the monomers a) to d) or i.a) to i.d) or ii.a) to ii.c) or iii.a) to iii.d) make(s) up at least 90 wt % of the adhesive component or components.

6. Method according to claim 1 , wherein the monomer mixture comprises at least the following monomers:
i.a) 50-99.5 wt % of at least one acrylic ester and/or methacrylic ester having the following formula:
CH 2 ═C(R 1 )(COOR 2 ), where

R 1 ═H and R 2 is a linear alkyl radical having 2 to 10 carbon atoms or is a branched, non-cyclic alkyl radical having at least 4 carbon atoms, and/or
R 1 ═CH 3 and R 2 is a linear alkyl radical having 8 to 10 carbon atoms or is a branched, non-cyclic alkyl radical having at least 10 carbon atoms;

i.b) 0 to 40 wt % of at least one acrylic ester and/or methacrylic ester having the following formula:
CH 2 ═C(R 3 )(COOR 4 ), where

R 3 ═H or CH 3 and R 4 is a linear alkyl radical having at least 12 carbon atoms;

i.c) 0.5-20 wt % of acrylic acid and/or methacrylic acid;
i.d) 0-25 wt % of at least one N-alkyl-substituted acrylamide, where the quantity figures are based in each case on the monomer mixture.

7. Method according to claim 1 , wherein the monomer mixture comprises at least the following monomers:
ii.a) 49.5-89.5 wt % of at least one acrylic ester and/or methacrylic ester and/or their free acids, having the following formula:
CH 2 ═C(R 5 )(COOR 6 ), where

R 5 ═H or CH 3 and R 6 is an alkyl radical having 1 to 10 carbon atoms or H and the homopolymer has a static glass transition temperature of <−30° C.;

ii.b) 10 to 40 wt % of at least one acrylic ester and/or methacrylic ester having the following formula:
CH 2 ═C(R 7 )(COOR 6 ), where

R 7 ═H or CH 3 and R 8 is a cyclic alkyl radical having at least 8 carbon atoms or is a linear alkyl radical having at least 12 carbon atoms and the homopolymer has a static glass transition temperature T g of at least 30° C.;

ii.c) 0.5 to 10 wt % of at least one acrylic ester and/or methacrylic ester and/or their free acids, having the following formula:
CH 2 ═C(R 9 )(COOR 10 ), where

R 9 ═H or CH 3 and R 10 ═H or an aliphatic radical having a functional group X, where X comprises COOH, OH, —NH(R 11 ), SH, SO 3 H, where R 11 ═H or a linear or branched alkyl radical having up to 10 carbon atoms, and the homopolymer has a static glass transition temperature T g of at least 30° C.,

where the quantity figures are based in each case on the monomer mixture.

8. Method according to claim 1 , wherein the monomer mixture comprises at least the following monomers:
iii.a) 25 to 82 wt % of linear acrylic esters having 2 to 10 carbon atoms in the alkyl radical;
iii.b) 10 to 40 wt % of branched, non-cyclic acrylic esters having a static glass transition temperature T g of not more than 0° C.;
iii.c) 8 to 15 wt % of acrylic acid, based on the total amount of monomers to be polymerized;
iii.d) optionally up to 10 wt % of further copolymerizable monomers, based on the total amount of monomers to be polymerized,

where the ratio of the linear acrylic esters to the branched acrylic esters is in the range from 1:6 to 10:1 mass fractions.

9. Method according to claim 1 , wherein the pressure-sensitive adhesive is in crosslinked form.

10. Method according to claim 1 , wherein the pressure-sensitive adhesive is provided in the form of an adhesive tape.

Assignees

• Tesa Se

Inventors

• Kerber Kristin
• Ellringmann Kai

Classifications

• C08K5/07

  Aldehydes; Ketones · CPC title

• B41N6/02 Primary

  Chemical means for fastening printing formes on mounting boards · CPC title

• C08K5/17

  Amines; Quaternary ammonium compounds · CPC title

• C09J5/00

  Adhesive processes in general; Adhesive processes not provided for elsewhere, e.g. relating to primers · CPC title

• C09J11/06

  organic · CPC title