US2017190874A1PendingUtilityA1

Stabilizer Compounds

54
Assignee: SOLVAY SPECIALTY POLYMERS USAPriority: May 21, 2014Filed: May 20, 2015Published: Jul 6, 2017
Est. expiryMay 21, 2034(~7.9 yrs left)· nominal 20-yr term from priority
C08K 5/3435C07D 211/46C08K 5/43
54
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

A piperidine-based stabilizer compound of formula (I) or (II) that imparts UV, thermal, and/or thermo-oxidative stability to polymer compositions and more specifically to aromatic polymers and polymer compositions thereof.

Claims

exact text as granted — not AI-modified
1 - 16 : (canceled) 
     
     
         17 . A stabilizer compound (SC) of formula (I) or formula (II): 
       
         
           
           
               
               
           
         
         wherein R J  is selected from the group consisting of —H, aliphatic groups and alkoxy groups, and 
         wherein each of R K , equal or different from each other and from R J , is selected from aliphatic groups, and 
         wherein R L  is a monovalent substituent selected from the group consisting of:
 a group of formula (Y-I): 
 
       
       
         
           
           
               
               
           
         
       
       and
   a group of formula (Y-II):   
 
       
         
           
           
               
               
           
         
         wherein Ri and Rm are the same or different from each other and are independently selected from the group consisting of —H, —CF 3 , —CN, —C(═O)NH 2 , —NO 2 , alkyl groups, perfluorinated groups, aryl groups, aryl amine groups, aryl ether groups, aryl sulfone groups, aryl thioether groups, fused aryl ring systems, sulfonic acids, carboxylic acids, phosphonic acids, sulfonic acid salts, carboxylic acid salts, and phosphonic acid salts, and 
         wherein Ri is either in an ortho, meta or para position, and 
         wherein Rm is either in an ortho or meta position, and 
         wherein Q is selected from the group consisting of a bond, and —SO 2 —, and 
         wherein G is —C(═O)NH 2 , 
         wherein R N  is a divalent substituent of formula (Z-I): 
       
       
         
           
           
               
               
           
         
         wherein Ri and Rm are the same or different from each other and are independently selected from the group consisting of —H, —CF 3 , —C(═O)NH 2 , —NO 2 , alkyl groups, perfluorinated groups, aryl groups, aryl amine groups, aryl ether groups, aryl sulfone groups, aryl thioether groups, fused aryl ring systems, sulfonic acids, carboxylic acids, phosphonic acids, sulfonic acid salts, carboxylic acid salts, and phosphonic acid salts, 
         wherein Ri and Rm are independently either in an ortho or meta position, and 
         wherein Q is selected from the group consisting of a bond, and —SO 2 —. 
       
     
     
         18 . The stabilizer compound (SC) of formula (I) of  claim 17 , wherein the stabilizer compound (SC) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
     
     
         19 . The stabilizer compound (SC) of formula (II) of  claim 17 , wherein the stabilizer compound (SC) is selected from the group consisting of: 
       
         
           
           
               
               
           
         
       
     
     
         20 . The stabilizer compound (SC) according to  claim 17 , wherein Rm is —H. 
     
     
         21 . A method for making the stabilizer compound of formula (I) of  claim 17 , comprising the step of reacting compounds of formulae (III) and (IV) together in the presence of a base; 
       
         
           
           
               
               
           
         
         wherein Xi is a halogen selected from the group consisting of chlorine, fluorine, bromine, and iodine, and 
         wherein R J , R K , R L  are as defined in  claim 17  for formula (I). 
       
     
     
         22 . A method for making the stabilizer compound of formula (II) of  claim 17 , comprising the step of reacting compounds of formulae (III) and (IV) together in the presence of a base; 
       
         
           
           
               
               
           
         
         wherein Xi or Xj are the same or independently selected halogens from the group consisting of chlorine, fluorine, bromine, and iodine, and 
         wherein R J , R K , R N  are as defined in  claim 17  for formula (II). 
       
     
     
         23 . The method of  claim 21 , wherein the reaction is carried out in a polar aprotic solvent. 
     
     
         24 . The method of  claim 23 , wherein the polar aprotic solvent is tetrahydrofuran and the reaction is carried out at a temperature of between 25° C. and 66° C. 
     
     
         25 . The method of  claim 23 , wherein the polar aprotic solvent is N-methylpyrrolidone and the reaction is carried out at a temperature of between 25° C. and 204° C. 
     
     
         26 . A polymer composition (P), comprising at least one stabilizer compound (SC) of  claim 17 , and at least one polymer selected from the group consisting of polyketones, poly(etherketone)s, poly(ethersulfone)s, and mixtures thereof. 
     
     
         27 . The polymer composition (P) of  claim 26 , wherein the polymer composition (P) further comprises at least another ingredient selected from the group consisting of dyes, pigments, fillers, UV stabilizers, light stabilizers, optical brighteners, and mixtures thereof. 
     
     
         28 . A method for stabilizing a polymer comprising adding at least one stabilizing compound (SC) of  claim 17  to at least one polymer. 
     
     
         29 . The method of  claim 28 , where the at least one stabilizing compound (SC) acts as an acid scavenger for the at least one polymer. 
     
     
         30 . An article comprising the polymer composition (P) of  claim 26 . 
     
     
         31 . The method of  claim 22 , wherein the reaction is carried out in a polar aprotic solvent. 
     
     
         32 . The method of  claim 31 , wherein the polar aprotic solvent is tetrahydrofuran and the reaction is carried out at a temperature of between 25° C. and 66° C. 
     
     
         33 . The method of  claim 31 , wherein the polar aprotic solvent is N-methylpyrrolidone and the reaction is carried out at a temperature of between 25° C. and 204° C.

Cited by (0)

No later patents cite this yet.

References (0)

No backward citations on record.