US2018298192A1PendingUtilityA1

Methods of manufacture of thermoplastic polymers

Assignee: SABIC GLOBAL TECHNOLOGIES BVPriority: Oct 14, 2015Filed: Oct 14, 2016Published: Oct 18, 2018
Est. expiryOct 14, 2035(~9.2 yrs left)· nominal 20-yr term from priority
C08L 81/06C08G 65/40C08G 75/23C08K 5/13C08K 5/3417C08G 75/00C08L 2207/04C08K 5/08C08L 81/00
58
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

A method of manufacture of a polyetherimide copolymer composition includes contacting a substituted phthalic anhydride and an organic diamine in the presence of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing solvents at a temperature of greater than 130° C. to provide a bis(phthalimide) composition comprising diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing solvents and a bis(phthalimide); and copolymerizing the bis(phthalimide), a substituted aromatic compound, and an alkali metal salt of a dihydroxy aromatic compound in the presence of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing to form a polyetherimide copolymer. The method does not require any catalyst either for the imidization or the polymerization.

Claims

exact text as granted — not AI-modified
1 . A method for the manufacture of a poly(arylene ether-sulfone), a poly(arylene ketone), or a copolymer thereof, the method comprising:
 polymerizing a substituted aromatic compound of the formula   
       
         
           
           
               
               
           
         
         and an alkali metal salt of a dihydroxy aromatic compound of the formula
   MO—Z—OM
 
 
       
       in the presence of diphenyl sulfone or sulfolane or a combination comprising at least one of the foregoing solvents to form a poly(arylene ether-sulfone), a poly(arylene ketone), or a copolymer thereof comprising structural units of the formula 
       
         
           
           
               
               
           
         
       
       wherein in the foregoing formulas
 X 1  and X 2  are each independently fluoro, chloro, bromo, iodo, nitro, or a combination comprising at least one of the foregoing; 
 M is an alkali metal; 
 Z is an aromatic C 6-24  monocyclic or polycyclic moiety optionally substituted with 1 to 6 C 1-8  alkyl groups, 1 to 8 halogen atoms, or a combination comprising at least one of the foregoing; 
 G is —C(O)— or —SO 2 —; and 
 m is 1 or 2. 
 
     
     
         2 . A method for the manufacture of a polyetherimide copolymer composition, the method comprising
 contacting a substituted phthalic anhydride and an organic diamine in the presence of diphenyl sulfone or sulfolane or a combination comprising at least one of the foregoing solvents at a temperature of greater than 130° C.,   wherein the substituted phthalic anhydride has a formula   
       
         
           
           
               
               
           
         
       
       and
 the organic diamine has a formula
   H 2 N—R—NH 2  
 
 
 
       to provide a bis(phthalimide) composition comprising diphenyl sulfone or sulfolane or a combination comprising at least one of the foregoing solvent and a bis(phthalimide) of the formula 
       
         
           
           
               
               
           
         
       
       and
 copolymerizing the bis(phthalimide), a substituted aromatic compound of the formula 
 
       
         
           
           
               
               
           
         
         and an alkali metal salt of a dihydroxy aromatic compound of the formula
   MO—Z—OM
 
 
       
       in the presence of diphenyl sulfone or sulfolane or a combination comprising at least one of the foregoing solvents to form a polyetherimide copolymer comprising structural units of the formulas 
       
         
           
           
               
               
           
         
       
       wherein in the foregoing formulae
 X, X 1 , and X 2  are each independently fluoro, chloro, bromo, iodo, nitro, or a combination comprising at least one of the foregoing; 
 R is an aromatic hydrocarbon group having 6 to 27 carbon atoms, a halogenated derivative thereof, a straight or branched chain alkylene group having 2 to 10 carbon atoms, a halogenated derivative thereof, a cycloalkylene group having 3 to 20 carbon atoms, a halogenated derivative thereof, —(C 6 H 10 ) z — wherein z is an integer from 1 to 4, an aromatic hydrocarbyl moiety having from 1 to 6 aromatic groups, and a divalent group of the formula 
 
       
         
           
           
               
               
           
         
         
           wherein Q 1  is —O—, —S—, —C(O)—, —SO—, —C y H 2y — wherein y is an integer from 1 to 5, or a combination comprising at least one of the foregoing; 
         
         M is an alkali metal; 
         Z is an aromatic C 6-24  monocyclic or polycyclic moiety optionally substituted with 1 to 6 C 1-8  alkyl groups, 1 to 8 halogen atoms, or a combination comprising at least one of the foregoing; 
         G is —C(O)— or —SO 2 —; and 
         m is 1 or 2. 
       
     
     
         3 . The method of  claim 2 , wherein the stoichiometric ratio of the substituted phthalic anhydride to the organic diamine is 1.95:1 to 2.05:1. 
     
     
         4 . The method of  claim 2 , wherein 
       
         
           
             
               
                 
                   weight 
                    
                   
                       
                   
                    
                   of 
                    
                   
                       
                   
                    
                   bis 
                    
                   
                       
                   
                    
                   
                     ( 
                     phthalimide 
                     ) 
                   
                 
                 
                   
                     
                       
                         
                           weight 
                            
                           
                               
                           
                            
                           of 
                            
                           
                               
                           
                            
                           bis 
                            
                           
                               
                           
                            
                           
                             ( 
                             phthalimide 
                             ) 
                           
                         
                         + 
                       
                     
                   
                   
                     
                       
                         weight 
                          
                         
                             
                         
                          
                         of 
                          
                         
                             
                         
                          
                         diphenyl 
                          
                         
                             
                         
                          
                         sulphone 
                          
                         
                             
                         
                          
                         of 
                          
                         
                             
                         
                          
                         sulfolane 
                       
                     
                   
                 
               
                
               
                 ( 
                 100 
                 ) 
               
             
           
         
       
       is 1 to 30%, specifically 15 to 25%, preferably 18 to 22%. 
     
     
         5 . The method of  claim 2 , comprising copolymerizing the bis(phthalimide), the substituted aromatic compound, and the alkali metal salt in the presence of an endcapping agent. 
     
     
         6 . The method of any  claim 2 , further comprising heating the diphenyl sulfone to a temperature of greater than 130° C., and combining the substituted phthalic anhydride and the organic diamine with the heated diphenyl sulfone. 
     
     
         7 . The method of  claim 2 , further comprising adding a monofunctional reactant to the substituted phthalic anhydride, the organic diamine, the diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing. 
     
     
         8 . The method of  claim 2 , wherein the contacting is conducted at a temperature of 130° C. to 250° C. 
     
     
         9 . The method of  claim 2 , wherein the contacting is conducted in the absence of an imidization catalyst. 
     
     
         10 . The method of  claim 2 , wherein the polymerization or copolymerization is conducted in the absence of a polymerization catalyst. 
     
     
         11 . The method of  claim 2 , wherein the polymerization or copolymerization is conducted in the presence of a polymerization catalyst. 
     
     
         12 . The method of  claim 2 , wherein the polymerization or copolymerization is conducted at a temperature of 130° C. to 250° C. 
     
     
         13 . The method of  claim 2 , wherein X is chloro, X 1  and X 2  are each independently chloro or fluoro, m is 1, and R is m-phenylene, p-phenylene, an arylene ether, a diarylsulfone, a group of the formula 
       
         
           
           
               
               
           
         
       
       wherein Q 1 - is a single bond, —O—, —S—, —C(O)—, —SO 2 —, —SO—, —C y H 2y  wherein y is an integer from 1 to 5, or a combination comprising at least one of the foregoing, preferably wherein R is m-phenylene, p-phenylene, para, para-diphenyl ether, 4,4-diphenylsulfone, or a combination comprising at least one of the foregoing. 
     
     
         14 . The method of  claim 2 , wherein the dihydroxy aromatic compound comprises bisphenol A, hydroquinone, biphenol, resorcinol, or a combination comprising at least one of the foregoing. 
     
     
         15 . The method of  claim 2 , wherein the substituted aromatic compound is 4,4′-difluorobenzophenone, 4,4′-dichlorodiphenylsulfone, or a combination comprising at least one of the foregoing. 
     
     
         16 . The method of  claim 2 , wherein the dihydroxy aromatic compound is dispersed in a solvent comprising ortho-dichlorobenzene, xylenes, toluene, diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing. 
     
     
         17 . The method of  claim 2 , the method comprising:
 contacting a substituted phthalic anhydride and an organic diamine in the presence of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing solvents at a temperature of 130° C. to 250° C.,   wherein the substituted phthalic anhydride has a formula   
       
         
           
           
               
               
           
         
       
       and
 the organic diamine has a formula
   H 2 N—R—NH 2  
 
 
 
       to provide a bis(phthalimide) composition comprising diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing solvents and a bis(phthalimide) of the formula 
       
         
           
           
               
               
           
         
       
       and
 copolymerizing the bis(phthalimide), a substituted aromatic compound of the formula 
 
       
         
           
           
               
               
           
         
         and a disodium salt or a dipotassium salt of bisphenol A in the presence of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing solvents to form a polyetherimide copolymer comprising structural units of the formulas 
       
       
         
           
           
               
               
           
         
       
       wherein in the foregoing formulae
 X is chloro; 
 X 1  and X 2  are each independently chloro, fluoro, bromo, iodo, or nitro; 
 R is m-phenylene, p-phenylene, p,p-diphenylether, or 4,4′-diphenylsulfone; 
 Z is 
 
       
         
           
           
               
               
           
         
       
       and
 G is —C(O)— or —SO 2 —. 
 
     
     
         18 . A polymer composition manufactured by a method of  claim 1 . 
     
     
         19 . The composition of  claim 18 , wherein the composition comprises a poly(arylene ether-sulfone), a poly(arylene ketone), or a copolymer thereof comprising structural units of the formula 
       
         
           
           
               
               
           
         
       
       wherein
 Z is an aromatic C 6-24  monocyclic or polycyclic moiety optionally substituted with 1 to 6 C 1-8  alkyl groups, 1 to 8 halogen atoms, or a combination comprising at least one of the foregoing; 
 each occurrence of G is independently —C(O)— or —SO 2 —; and 
 m is 1 or 2; and 
 
       wherein
 the composition comprises one or more of 
 greater than 0.1 parts per million of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing, or 
 greater than 1 part per million of sodium or potassium, or a yellowness index of less than 300. 
 
     
     
         20 . A polyetherimide copolymer composition wherein the polyetherimide copolymer comprises structural units of the formulas 
       
         
           
           
               
               
           
         
       
       wherein
 R is an aromatic hydrocarbon group having 6 to 27 carbon atoms, a halogenated derivative thereof, a straight or branched chain alkylene group having 2 to 10 carbon atoms, a halogenated derivative thereof, a cycloalkylene group having 3 to 20 carbon atoms, a halogenated derivative thereof, —(C 6 H 10 ) z — wherein z is an integer from 1 to 4, an aromatic hydrocarbyl moiety having from 1 to 6 aromatic groups, and a divalent group of the formula 
 
       
         
           
           
               
               
           
         
       
       wherein Q 1  is —O—, —S—, —C(O)—, —SO 2 —, —SO—, —C y H 2y — wherein y is an integer from 1 to 5, or a combination comprising at least one of the foregoing; and
 Z is an aromatic C 6-24  monocyclic or polycyclic moiety optionally substituted with 1 to 6 C 1-8  alkyl groups, 1 to 8 halogen atoms, or a combination comprising at least one of the foregoing; 
 G is —C(O)— or —SO 2 —; and 
 m is 1 or 2; 
 
       preferably wherein
 R is m-phenylene, p-phenylene, p,p-diphenylether, or 4,4′-diphenylsulfone; 
 Z is 
 
       
         
           
           
               
               
           
         
       
       and
 m is 1; and 
 
       wherein
 the composition comprises one or more of 
 greater than 0.1 parts per million of diphenyl sulfone, sulfolane, or a combination comprising at least one of the foregoing, or 
 greater than 1 part per million of sodium or potassium, or a yellowness index of less than 300.

Join the waitlist — get patent alerts

Track US2018298192A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.