General purpose siloxane release coatings

Claim 2

A coated sheet material comprising: (a) a flexible sheet; and (b) a release coating covering at least a portion of one major surface of said flexible sheet wherein said release coating comprises a block copolymer having a formula selected from the group consisting of AB and ABA, wherein A comprises at least one vinyl polymeric block, wherein each polymeric block consists essentially of polymerized free radically polymerizable monomer, wherein each polymeric block has a T g or T m above about -20° C. and wherein A comprises at least about 40 weight percent of said block copolymer, wherein B is a siloxane polymeric block having a number average molecular weight above about 1000, and wherein the weight percent of the siloxane polymeric block is great enough to provide said block copolymer with a surface release value not greater than about 50 Newtons/dm; wherein said block polymer has the formula ##STR44## and is made by the utilization of an iniferter represented by the formula ##STR45## wherein:

Claim 3

T and X are organic groups selected so that the T-X bond is capable of dissociating upon being subject to a radiant energy source to form a terminator free radical of the formula T. and an initiator free radical of the formula ##STR46## said initiator free radical being sufficiently reactive to initiate free radical polymerization of free radically polymerizable monomer and said terminator free radical being insufficiently capable of initiating free radical polymerization of free radically polymerizable monomer but capable of rejoining with said initiator free radically or a free radical polymer segment free radically polymerized with said initiator free radical; R 1 , R 2 , R 5 and R 6 are monovalent moieties selected from the group consisting of hydrogen, C 1-4 alkyl, C 1-4 alkoxy and aryl which can be the same or are different; R 3 and R 4 are monovalent moieties which can be the same or different selected from the group consisting of C 1-4 alkyl, C 1-4 fluoroalkyl including at least one fluorine atom and aryl; R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are selected so that they do not prevent said initiator free radical from initiating free radical polymerization or the combining of said terminator free radical with said initiator free radical or a polymer free radical segment including said initiator free radical; Y is selected from the group consisting of --X--T and --Z wherein X and T are defined above and Z is an organic moiety that will not dissociate to form free radicals when subjected to said energy source; L is selected from the group consisting of --X--A--T and --Z wherein X and T are defined above and Z is an organic moiety that will not dissociate to form free radicals when subjected to said energy source; Y 1 is selected from the group consisting of -X. and Z; and m is an integer of at least 10.

Claim 4

T and X are organic groups selected so that the T-X bond is capable of dissociating upon being subject to a radiant energy source to form a terminator free radical of the formula T. and an initiator free radical of the formula ##STR46## said initiator free radical being sufficiently reactive to initiate free radical polymerization of free radically polymerizable monomer and said terminator free radical being insufficiently capable of initiating free radical polymerization of free radically polymerizable monomer but capable of rejoining with said initiator free radically or a free radical polymer segment free radically polymerized with said initiator free radical; R 1 , R 2 , R 5 and R 6 are monovalent moieties selected from the group consisting of hydrogen, C 1-4 alkyl, C 1-4 alkoxy and aryl which can be the same or are different; R 3 and R 4 are monovalent moieties which can be the same or different selected from the group consisting of C 1-4 alkyl, C 1-4 fluoroalkyl including at least one fluorine atom and aryl; R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are selected so that they do not prevent said initiator free radical from initiating free radical polymerization or the combining of said terminator free radical with said initiator free radical or a polymer free radical segment including said initiator free radical; Y is selected from the group consisting of --X--T and --Z wherein X and T are defined above and Z is an organic moiety that will not dissociate to form free radicals when subjected to said energy source; L is selected from the group consisting of --X--A--T and --Z wherein X and T are defined above and Z is an organic moiety that will not dissociate to form free radicals when subjected to said energy source; Y 1 is selected from the group consisting of -X. and Z; and m is an integer of at least 10.

Claim 5

The coated sheet material of claim 1 wherein the siloxane polymeric block has a number average molecular weight of about 1000 to about 15,000.

Claim 6

The coated sheet material of claim 1 wherein the siloxane polymeric block has a number average molecular weight of about 2,000 to about 10,000.

Claim 7

The coated sheet material of claim 1 wherein the siloxane polymeric block is present at a weight percent of about 2 to about 60 percent of said block polymer.

Claim 8

The coated sheet material of claim 1 wherein said vinyl polymer block or blocks comprising A are formed from monomers selected from the group consisting of methyl acrylate, acrylic acid, vinyl acetate, methyl methacrylate, N-vinyl pyrrolidone, hydroxypropyl acrylate, hydroxyethyl acrylate, styrene, 2-ethoxyethyl acrylate, and mixtures thereof.

Claim 9

The coated sheet material of claim 1 wherein said vinyl polymeric block or blocks possess ionic functionality of less than about 15% by weight of said copolymer.

Claim 10

The coated sheet material of claim 6 wherein said ionic content comprises above 2% by weight of said copolymer.

Claim 11

The coated sheet material of claim 6 wherein said ionic content comprises above 4% by weight of said copolymer.

Claim 12

The coated sheet material of claim 1 wherein said vinyl polymeric block A has a hydrated Tg between -15° C. and ±35° C. and the temperature difference between the hydrated Tg and actual Tg is at least 20° C. and wherein a coating of said release coating has a receding contact angle with water of less than 25° such that said release coating is capable of being written on effectively with both solvent based ink and water based ink.

Claim 13

The coated sheet material of claim 1 wherein the release agent is on one side of the sheet and an adhesive is on the other side.

Claim 14

The coated sheet material of claim 10 wherein the adhesive is a normally tacky and pressure-sensitive adhesive.

Claim 15

A stack of superimposed sheets of the coated sheet material of claim 11, the pressure-sensitive adhesive on each sheet being in contact with the release agent on an immediately adjacent sheet.

Claim 16

The coated sheet material of claim 11 wound convolutely on itself about a core to form a roll.

Claim 17

The coated sheet material of claim 1 wherein A comprises polymer block A' which consists essentially of a polymerized free radically polymerizable first monomer charge and polymer block A" which consists essentially of a polymerized free radically polymerizable second monomer charge.

Claim 18

The coated sheet material of claim 1 wherein A comprises a copolymer block which consists essentially of methyl acrylate and acrylic acid.

Claim 19

The coated sheet material of claim 1 wherein said release coating further comprises a compatible copolymer or homopolymer blended with said block copolymer.