US2014224424A1PendingUtilityA1

Inhibitor combination, resin mixture containing same and use of same

Assignee: HILTI AGPriority: Jun 9, 2011Filed: Apr 21, 2014Published: Aug 14, 2014
Est. expiryJun 9, 2031(~4.9 yrs left)· nominal 20-yr term from priority
Y10T428/13C04B 40/065C04B 24/02C04B 40/0039C04B 28/06C08L 33/10C04B 24/128B65D 25/00C04B 26/02C04B 40/0658C04B 2111/00715C09K 15/30
47
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Claims

Abstract

The use of a mixture of 5-pyrimidinol derivatives with sterically hindered phenol derivatives for adjusting the reactivity and the gel time of resin mixtures and reactive resin mortars based on radically polymerizable compounds is described. Furthermore, a resin mixture containing the inhibitor combination, a reactive resin mortar containing this resin mixture and two-component mortar systems with the reactive resin mortar according to the invention and a hardener with improved stability in storage and good low-temperature hardening properties are also described. The resin mixture according to the invention is suitable in particular for chemical fastening of construction elements in boreholes in various substrates.

Claims

exact text as granted — not AI-modified
1 . A method of adjusting the reactivity and the gel time of resin mixtures based on radically polymerizable compounds, comprising adding a combination of a compound of general formula (I): 
       
         
           
           
               
               
           
         
       
       wherein R 1  and R 2  independently of one another denote hydrogen or a branched or unbranched C 1 -C 20  alkyl group, X is —OR 3  or —NR 3   2 , where R 3  is a branched or unbranched C 1 -C 20  alkyl group or a C 2 -C 4  polyalkylene oxide group, with a compound of general formula (II) 
       
         
           
           
               
               
           
         
       
       wherein R denotes hydrogen, a branched or unbranched C 1 -C 18  alkyl group or —OR 3  or —NR 3   2 , where R 3  denotes a branched or unbranched C 1 -C 20  alkyl group, R′ is hydrogen, a branched or unbranched C 1 -C 18  alkyl group and R″ is a branched or unbranched C 1 -C 18  alkyl group, for adjusting the reactivity and the gel time of resin mixtures based on radically polymerizable compounds. 
     
     
         2 . The method according to  claim 1 , wherein R 1  and R 2  in formula (I), independently of one another, are hydrogen or a branched or unbranched C 1 -C 8  alkyl group. 
     
     
         3 . The method according to  claim 2 , wherein R 1  and R 2  in formula (I), independently of one another are hydrogen or methyl. 
     
     
         4 . The method according to  claim 3 , wherein the compound of formula (I) is 2-(dimethylamino)pyrimidin-5-ol, 2-(dimethylamino)-4,6-dimethylpyrimidin-5 -ol or 4,6-dimethyl-2-(octyloxy)pyrimidin-5-ol. 
     
     
         5 . The method according to  claim 1 , wherein the compound of formula (II) is 2,6-di-tert-butyl-4-methylphenol or 2,6-di-tert-butyl-4-hydroxyanisole. 
     
     
         6 . (canceled) 
     
     
         7 . The method according to  claim 1 , wherein the molar ratio of the component of formula (I) to the compound of formula (II) is 1:1 to 1:10. 
     
     
         8 . A resin mixture comprising at least one radically polymerizable compound, optionally a reactive diluent and an agent for adjusting the reactivity and the gel time, wherein the agent for adjusting the reactivity and the gel time is a combination of a compound of general formula (I) 
       
         
           
           
               
               
           
         
       
       wherein R 1  and R 2  independently of one another denote hydrogen or a branched or unbranched C 1 -C 20  alkyl group, and X is —OR 3  or —NR 3   2 , where R 3  is a branched or unbranched C 1 -C 20  alkyl group or a C 2 -C 4  polyalkylene oxide group, with a compound of general formula (II) 
       
         
           
           
               
               
           
         
       
       wherein R denotes hydrogen, a branched or unbranched C 1 -C 18  alkyl group or —OR 3  or —NR 3   2 , where R 3  denotes a branched or unbranched C 1 -C 20  alkyl group, R′ is hydrogen, a branched or unbranched C 1 -C 18  alkyl group and R″ is a branched or unbranched C 1 -C 18  alkyl group. 
     
     
         9 . The resin mixture according to  claim 8 , wherein R 1  and R 2  in formula (I) independently of one another are hydrogen or a branched or unbranched C 1 -C 8  alkyl group. 
     
     
         10 . The resin mixture according to  claim 9 , wherein R 1  and R 2  in formula (I) independently of one another are hydrogen or methyl. 
     
     
         11 . The resin mixture according to  claim 10 , wherein an agent (c) for adjusting the reactivity and the gel time is 2-(dimethylamino)pyrimidin-5-ol, 2-(dimethylamino)-4,6-dimethylpyrimidin-5-ol or 4,6-dimethyl-2-(octyloxy)pyrimidin-5-ol. 
     
     
         12 . The resin mixture according to  claim 8 , wherein the compound of formula (II) is 2,6-di-tert-butyl-4-methylphenol or 2,6-di-tert-butyl-4-hydroxyanisole. 
     
     
         13 . (canceled) 
     
     
         14 . The resin mixture according to  claim 8 , wherein the molar ratio of the component of formula (I) to the compound of formula (II) is 1:1 to 1:10. 
     
     
         15 . The resin mixture according to  claim 8 , wherein the resin mixture also contains an accelerator for the curing agent. 
     
     
         16 . A reactive resin mortar, comprising the resin mixture according to  claim 8  and inorganic additives. 
     
     
         17 . A two-component mortar system, comprising the reactive resin mortar according to  claim 16  as component A and a hardener arranged separately to inhibit reaction as component B. 
     
     
         18 . The two-component mortar system according to  claim 17 , wherein the hardener contains an organic or inorganic peroxide as the curing agent. 
     
     
         19 . The two-component mortar system according to  claim 17 , wherein the hardener also contains inorganic additives. 
     
     
         20 . The two-component mortar system according to  claim 17 , wherein component A additionally contains a hydraulically setting or polycondensable inorganic compound in addition to the reactor resin mortar and component B additionally contains water in addition to the curing agent. 
     
     
         21 . A method of chemical fastening comprising applying the two-component mortar system according to  claim 17  for chemical fastening. 
     
     
         22 . A shell, cartridge or film bag containing a two-component mortar system according to  claim 17  comprising two or more separate chambers in which the reactive resin mortar and/or hardener is/are arranged. 
     
     
         23 . The resin mixture of  claim 8  wherein the resin mixture further comprises a reactive diluents and an agent for adjusting the reactivity and the gel time.

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