US2012045624A1PendingUtilityA1

Aqueous laser-sensitive composition for marking substrates

Assignee: CAMPBELL JONATHANPriority: Oct 27, 2008Filed: Oct 16, 2009Published: Feb 23, 2012
Est. expiryOct 27, 2028(~2.3 yrs left)· nominal 20-yr term from priority
B41M 5/3275B41M 5/3372B41M 5/26C09D 133/02B41M 5/3336Y10T428/24802C08K 5/1535C08F 220/12B41M 2205/04
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Claims

Abstract

Aqueous composition comprising a colour former, a developer, and a binder, wherein (a) the weight ratio between the developer and the colour former is in the range of from 1 to 5; (b) the binder comprises an acrylate binder, comprising acrylic acid and styrene, and at least one additional monomer selected from the group consisting of α-methyl styrene, ethyl acrylate and 2-ethylhexyl acrylate; and (c) the colour former and/or the developer are present in an un-encapsulated form; a process for the preparation of these compositions, substrates coated with this composition and a process for its preparation, and a process for preparing a marked substrate using this composition.

Claims

exact text as granted — not AI-modified
1 . An aqueous composition comprising a colour former, a developer, and a binder, wherein
 (a) the weight ratio between the developer and the colour former is in the range of from 1 to 5;   (b) the binder comprises an acrylate binder, comprising acrylic acid and styrene, and at least one additional monomer selected from the group consisting of α-methyl styrene, ethyl acrylate and 2-ethylhexyl acrylate; and   (c) the colour former and/or the developer are present in an un-encapsulated form.   
     
     
         2 . Composition according to  claim 1 , wherein the colour former is a fluoran. 
     
     
         3 . Composition according to  claim 2 , wherein the fluoran is at least one selected from the group consisting of 3-dibutylamino-6-methyl-7-anilinofluoran, 3-diethylamino-6-methyl-7-anilinofluoran, 3-(N-ethyl-N-isoamylamino)-6-methyl-7-anilinofluoran, 3-dipentylamino-6-methyl-7-anilinofluoran, and 3-(N-ethyl-N-p-tolylamino)-6-methyl-7-anilinofluoran. 
     
     
         4 . Composition according  claim 1 , wherein the developer is selected from the group consisting of sulfonylurea derivatives, 4,4′-bis(p-toluenesulphonylaminocarbonylamino)diphenylmethane), 4,4′-bisphenol sulfone, 2,4′-dihydroxydiphenylsulfone, 4-hydroxy-4′-isopropoxydiphenylsulfone, 4-hydroxybenzoate derivative of a polypentaerythritol compound with CAS number 378244-93-0; phenol, 4,4′-sulfonylbis-polymer with 1,1′-oxobis(2-chloroethane); N,N′-[sulfonylbis[4,1-phenylene iminocarbonylimino(methylphenylene)]]bis-, C,C′-diphenyl ester; ZnCl 2 , octylammonium stearate and ammonium stearate. 
     
     
         5 . Composition according to  claim 4 , wherein the developer is N-(p-toluenesulfonyl)-N′-3-(ptoluenesulfonyloxyphenyl)urea or phenol, 4,4′-sulfonylbis-polymer with 1,1′-oxobis(2-chloroethane). 
     
     
         6 . Composition according  claim 1 , wherein the weight ratio between the developer and the colour forming compound is in the range of from 1.5 to 3. 
     
     
         7 . A process for preparing the composition of  claim 1 , which comprises the step of mixing a colour former and a developer in a weight ratio in the range of from 1 to 5; a binder comprising an acrylate binder, comprising acrylic acid and styrene, and at least one additional monomer selected from the group consisting of α-methyl styrene, ethyl acrylate and 2-ethylhexyl acrylate; and wherein the colour former and/or the developer are present in an un-encapsulated form. 
     
     
         8 . A substrate coated with the composition of  claim 1 . 
     
     
         9 . A process for preparing a coated substrate, which comprises the step of coating a substrate with the composition of  claim 1 . 
     
     
         10 . A process for preparing a marked substrate, which comprises the steps of i) coating a substrate with the composition of  claim 1 , and ii) exposing those parts of the coated substrate, where a marking is intended, to energy in order to generate a marking. 
     
     
         11 . The process of  claim 10 , wherein the energy is selected from the group consisting of UV, IR, visible and microwave irradiation. 
     
     
         12 . A marked substrate, which is obtained by the process of  claim 10 . 
     
     
         13 . A substrate coated with the composition of  claim 2 . 
     
     
         14 . A process for preparing a coated substrate, which comprises the step of coating a substrate with the composition of  claim 2 . 
     
     
         15 . A process for preparing a marked substrate, which comprises the steps of i) coating a substrate with the composition of  claim 2 , and ii) exposing those parts of the coated substrate, where a marking is intended, to energy in order to generate a marking.

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