US2005054759A1PendingUtilityA1

Thermoplastic elastomer compositions containing a phase change solvent and selected processing oils

Assignee: PROCTER & GAMBLEPriority: Jul 31, 2002Filed: Sep 7, 2004Published: Mar 10, 2005
Est. expiryJul 31, 2022(expired)· nominal 20-yr term from priority
C08G 64/22C08G 18/282C07C 69/82C08J 3/091C08G 18/0852C07C 69/76C08K 5/0016C08G 71/00C08K 5/12C08G 63/18C07C 67/14C08G 18/3206
42
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Claims

Abstract

Novel elastomeric compositions which contain at least one thermoplastic elastomer and at least one phase change solvent and at least one processing oil. The presence of particular processing oils, e.g., poly(alphaolefins), provide a means to increase mechanical properties compared to commercially available mineral oils. The oils of the present invention are chosen as to minimize the depression of glass transition temperature of the hard-block of the thermoplastic elastomer. The phase change behavior of these materials produce elastomeric compositions that exhibit lowered viscosity and lowered processing temperature without substantially compromising the mechanical properties of the elastomeric composition.

Claims

exact text as granted — not AI-modified
1 . A composition comprising: 
 a) from about 1 to about 98 wt % a thermoplastic elastomer, which is a block copolymer having at least one soft block and at least one hard block;    b) from about 1 to about 70 wt % a phase change solvent having the general formula:        R ′- P   y -( Q - P   x ) n−1 - Q - P   y - R   (I);    R ′- P   y -( Q - P   x ) n - R   (II);    R ′-( Q - P   x ) n - R   (III);    R ′-( Q - P   x ) n−1 - Q - P   y - R   (IV);    R ′-( Q - P   x ) n−1 - Q - R   (V); or  a mixture thereof;       wherein Q is a substituted or unsubstituted difunctional aromatic moiety; P is CH 2 ; R and R′ are the same or different and are independently selected from H, CH 3 , COOH, CONHR 1 , CONR 1 R 2 , NHR 3 , NR 3 R 4 , hydroxy, or C 1 -C 30  alkoxy; wherein R 1 , R 2 , R 3  and R 4  are the same or different and are independently selected from H or linear or branched alkyl from C 1 -C30; x is an integer from 1 to 30; y is an integer from 1 to 30; and n is an integer from 2 to 7; and    c) from about 1 to about 70 wt % of a processing oil producing a glass transition temperature of greater than about 85° C. for a polystyrene homopolymer.    
     
     
         2 . The composition of  claim 1  wherein the processing oil producing a glass transition temperature of greater than about 87° C. for a polystyrene homopolymer.  
     
     
         3 . The composition of  claim 1  wherein the processing oil producing a glass transition temperature of greater than about 90° C. for a polystyrene homopolymer.  
     
     
         4 . The composition of  claim 1  wherein the processing oil is selected from the group consisting of poly (alpha olefins),olefinic oligomers, mineral oils, paraffinic oils, isoparaffinic oils, naphthenic oils, petrolatum, waxes, or mixtures thereof.  
     
     
         5 . The composition of  claim 1  wherein the synthetic processing oil is a poly (alpha olefin).  
     
     
         6 . The composition of  claim 5  wherein the poly(alpha olefin) is selected from the group consisting of polydodecenes, polydecenes, polyoctenes, polybutylenes, polybutenes, and mixtures thereof.  
     
     
         7 . The composition of  claim 5  wherein the poly(alpha olefin) is selected from the group consisting of poly(1-decene), poly(1-dodecene), poly(1-octene), and mixtures thereof.  
     
     
         8 . The composition of  claim 1  wherein the processing oil is a mixture of a synthetic oil and a natural oil.  
     
     
         9 . The composition of  claim 8  wherein the synthetic oil comprises at least about 40% of the processing oil mixture.  
     
     
         10 . The composition of  claim 1  wherein the processing oil has a molecular weight in the range of from about 500 to about 3000 g/mol.  
     
     
         11 . The composition of  claim 1  additionally comprising from about 0.1 to about 50 wt % a nucleating agent.  
     
     
         12 . The composition of  claim 1  additionally comprising from about 1 to about 50 wt % a thermoplastic polymer.  
     
     
         13 . The composition of  claim 1  wherein the composition has a shear viscosity of about 0.1 to about 3000 Pa·s at 190° C. and 1 sec −1 .  
     
     
         14 . A composition comprising: 
 a) from about 1 to about 99 wt % a thermoplastic elastomer, which is a block copolymer having at least one soft block and at least one hard block;    d) from about 1 to about 70 wt % a phase change solvent having the general formula:        R ′- P   y -( Q - P   x ) n−1 - Q - P   y - R   (I);    R ′- P   y -( Q - P   x ) n - R   (II);    R ′-( Q - P   x ) n - R   (III);    R ′-( Q - P   x ) n−1 - Q - P   y - R   (IV);    R ′-( Q - P   x ) n−1 - Q - R   (V); or  a mixture thereof;       wherein Q is a substituted or unsubstituted difunctional aromatic moiety; P is CH 2 ; R and R′ are the same or different and are independently selected from H, CH 3 , COOH, CONHR 1 , CONR 1 R 2 , NHR 3 , NR 3 R 4 , hydroxy, or C1-C30 alkoxy; wherein R 1 , R 2 , R 3  and R 4  are the same or different and are independently selected from H or linear or branched alkyl from C1-C30; x is an integer from 1 to 30; y is an integer from 1 to 30; and n is an integer from 2 to 7; and c) from about 1 to about 70 wt % of a processing oil composition comprising a synthetic oil and a natural oil and producing a glass transition temperature of greater than about 85° C. for a polystyrene homopolymer.    
     
     
         15 . A method of lowering the viscosity and improving the processability of a thermoplastic elastomer, the method comprising the step of: 
 blending from about 1 to about 99 wt % of the thermoplastic elastomer, which is a block copolymer having at least soft block and at least one hard block, from about 1 to about 70 wt % of a phase change solvent having the general formula (1) - (V) of  claim 1 , or a mixture thereof, and from about 1 to about 70 wt % of a processing oil producing a glass transition temperature of greater than about 85° C. for a polystyrene homopolymer to form an elastomeric composition;    wherein the shear viscosity of the elastomeric composition is lower than the shear viscosity of the thermoplastic elastomer when measured at 190° C. and 1 sec −1 .    
     
     
         16 . The method of  claim 15  wherein the elastomeric composition has a shear viscosity of about 0.1 to about 3000 Pa·s at 190° C. and 1 sec −1 .  
     
     
         17 . The method of  claim 15  further comprising blending one or more additional ingredient with the thermoplastic elastomer, the phase change solvent, and processing oil, wherein the additional ingredient is selected from the group consisting of: 
 from about 0.1 to about 50 wt % of a nucleating agent;    from about 1 to about 50 wt % of a thermoplastic polymer; and    mixtures thereof.    
     
     
         18 . The method of  claim 15  wherein the processing oil has a molecular weight in the range of from about 500 to about 3000 g/mol  
     
     
         19 . The method of  claim 15  wherein the processing oil comprises 50% of a mineral oil and 50% of a synthetic oil.  
     
     
         20 . The method of  claim 19  wherein the synthetic oil is a poly (alpha olefin).

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