Cross-linked silicone gels; products containing the same; and methods of manufacture thereof

• US 6,936,686 B2
• Filed: 08/22/2003
• Issued: 08/30/2005
• Est. Priority Date: 12/11/2002
• Status: Active Grant

• Current Assignee: Alzo International, Inc.
• Original Assignee: Nutech Corp.
• Inventors: Awad, Nagi M.
• Primary Examiner(s): Moore, Margaret G.
• Assistant Examiner(s): Zimmer, Marc S
• Application Number:
  US10/646,122
• Publication Number:
  US 20040138376A1
• Time in Patent Office: 739 Days
• Field of Search: 424/486, 524266-268, 524/379, 524/588, 528/31, 528/32, 528/502.F, 528/15, 428/447
• US Class Current: 528/502.00F
• CPC Class Codes: A61K 8/042 Gels
• CPC Class Codes: A61K 8/895 containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
• CPC Class Codes: A61Q 15/00 Anti-perspirants or body deodorants deodorisation of air A61L9/00
• CPC Class Codes: A61Q 17/04 Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
• CPC Class Codes: A61Q 19/00 Preparations for care of the skin
• CPC Class Codes: C08G 77/12 containing silicon bound to hydrogen C08G77/045 takes precedence
• CPC Class Codes: C08G 77/20 containing silicon bound to unsaturated aliphatic groups C08G77/045 takes precedence
• CPC Class Codes: C08J 2383/04 Polysiloxanes
• CPC Class Codes: C08J 3/09 in organic liquids
• CPC Class Codes: C08L 83/00 Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
• CPC Class Codes: C08L 83/04 Polysiloxanes

Abstract

A polymerization product of an polyorganohydrosiloxane having a molecular weight of about 3500 to about 4000 and 6-7 Si—H bonds per molecule with a lower alkylene terminated polydimethylsiloxane having a molecular weight of about 20,000 to about 25,000 in the presence of a medium selected from low viscosity silicone oils, hydrocarbon oils typically with the aid of a hydrosilylation catalyst, where the amounts of the siloxanes are chosen such that the reaction product constitutes about 3% to about 15% of the cross-linked polymer and about 97 to about 85% of the reaction medium. The resultant gel is milled in a colloid mill, and if desired, diluted to a concentration of about 3% to about 8% with a diluent selected from the group consisting of low viscosity silicone oil, hydrocarbon oil, lower alkanol, or mixtures thereof. The so produced gel is useable as is or can be formulated into more complex cosmetic formulations having about 65% to about 99.9% of the gel, about 0.1% to about 30% of other non-diluent cosmetic materials (materials that are not low viscosity silicone oil, hydrocarbon oil, or lower alkanol), and up to about 5% lower alkanol.

Claims

1. A cross-linked silicone gel substantially free of SiO₂ groups, substantially free of SiO_1.5 groups, and substantially free of polyalkyleneoxide groups, comprising a cross-linked polymerization product of

(A) (i) an α

,ω

-di loweralkenyl terminated polyorganosiloxane of formula I

 

having a molecular weight of about 20,000 to about 25,000 with n being about 265 to about 340 and each R1 being independently H, or an alkyl group of 1 or 3 carbons and

(ii) optionally an α

,ω

-di ethylene terminated polydiphenyldimethylorganosiloxane; and

(B) a polyorganohydosiloxane of formula II

 

where the molecular weight of reactant II is about 3500 to 4000;

q is about 5 to about 9;

p is about 40 to about 50, and each R2 is independently an alkyl of 1-3 carbon atoms;

said polymerization product being polymerized in the presence of a medium selected from the group consisting of hydrocarbon oils, and mixtures thereof; and

(C) said medium

wherein said polymerization takes place initially with mixing and said mixing is halted when gelling is visibly seen.

2. The silicone gel of claim 1 wherein after said polymerization, said gel is subjected to milling, said milling being conducted while said gel is in the swollen state.

3. The silicone gel of claim 2 wherein said milling is conducted in a colloid mill.

4. The silicone gel of claim 1 comprising about 3% to about 15% of said polymer and about 97% to about 85% of said medium.

5. The silicone gel of claim 1 which is further diluted with a diluent selected from the group consisting of hydrocarbon oils, lower alkanols, and mixtures thereof.

6. A cosmetic formulation comprising about 65% to about 99.9% of the silicone gel of claim 1, about 0.1% to about 30% of at least one cosmetically acceptable ingredient which cosmetic ingredient is not a low viscosity silicone oil, a hydrocarbon oil, or a lower alkanol, or mixtures thereof;

and up to about 10% of a diluent selected from the group consisting of low viscosity silicone oils, hydrocarbon oils, and lower alkanols.

21. A cosmetic composition incorporating said silicone gel of claim 1.

26. The silicone gel of claim 1 which is substantially clear.

28. A method of use of the silicone gel of claim 1 comprising applying said gel to a rubber or rubber-like surface.

29. The method of claim 28 wherein said rubber or rubber-like surface is a member selected from the group consisting of tires, sealing rings, gaskets, weatherstripping, and caulking.

30. The method of claim 29 wherein said rubber or rubber-like surface is an automotive tire.

31. A composition comprising the silicone gel of claim 1 along with components suitable for application to rubber or rubber-like surfaces.

7. A method of making a clear silicone gel comprising

(A) (i) polymerizing in the presence of a hydrosilylation polymerization catalyst and a medium selected from the group consisting of hydrocarbon oils, and mixtures thereof

(1) an α

,ω

-di lower alkenyl terminated polyorganosiloxane of formula I

 

having a molecular weight of about 20,000 to about 25,000 with n being about 265 to about 340 and each R1 being independently H, or an alkyl group of 1 or 3 carbons and

(ii) optionally an α

,ω

-di ethylene terminated polydiphenyldimethylorganosiloxane and

(2) a polyorganohydrosiloxane of formula II

 

where the molecular weight of reactant II is about 3500 to 4000;

q is about 5 to about 9;

p is about 40 to about 50; and

each R2 is independently an alkyl having 1-3 carbon atoms resulting in a swollen gel;

(B) milling said swollen gel; and

(C) optionally diluting the result of step (B) with a diluent selected from the group consisting of low viscosity silicone oils, hydrocarbon oils, and lower alkanols;

wherein said polymerization takes place initially with mixing and said mixing is halted when gelling is visibly seen.

8. The process of claim 7 wherein said milling said swollen gel step takes place in a colloid mill.

9. The process of claim 7 wherein said hydrosilylation catalyst is zero valent platinum divinyl complex.

10. The process of claim 7 wherein said polymerization reaction takes place at about 20°

C. to about 50°

C.

11. The process of claim 7 wherein said reaction is permitted to proceed for at least 2 hours.

12. The process of claim 7 wherein said reaction is permitted to proceed for at least 3 hours.

13. The process of claim 7 wherein said reaction is permitted to proceed for at least 4 hours.

14. The process of claim 7 wherein said polymerization reaction is permitted to take place in the substantial absence of shearing forces.

15. The process of claim 7 further comprising adjusting the viscosity of gel by diluting said gel with a diluent selected from the group consisting of low viscosity silicone oils, hydrocarbon oils, and lower alkanols to result in a diluted gel.

16. The process of claim 15 further comprising passing said diluted gel through a colloid mill.

17. The silicone gel resulting from the process of claim 7, provided that when said optional dilution step (C) of claim 7 is utilized, said diluent is selected from the group consisting of hydrocarbon oils and lower alkanols.

18. The silicone gel of claim 17 wherein said milling said swollen gel step takes place in a colloid mill.

19. The silicone gel of claim 17 further comprising adjusting the viscosity of said gel by diluting said gel with a diluent selected from the group consisting of hydrocarbon oils, and lower alkanols to result in a diluted gel.

20. The silicone gel of claim 19 further comprising passing said diluted gel through a colloid mill.

22. A cosmetic composition incorporating the silicone gel of claim 17.

23. A cosmetic composition incorporating the silicone gel of claim 18.

24. A cosmetic composition incorporating the silicone gel of claim 19.

25. A cosmetic composition incorporating the silicone gel of claim 20.

27. The silicone gel of claim 20 which is substantially clear.

32. A cross-linked silicone gel substantially free of SiO₂ groups, substantially free of SiO_1.5 groups, and substantially free of polyalkyleneoxide groups, comprising a cross-linked polymerization product of

(A) (i) an α

,ω

-di lower alkenyl terminated polyorganosiloxane of formula I

 

having a molecular weight of about 20,000 to about 25,000 with n being about 265 to about 340 and each R1 being independently H, or an alkyl group of 1 or 3 carbons and

(ii) optionally an α

,ω

-di ethylene terminated polydiphenyldimethylorganosiloxane; and

(B) a polyorganohydrosiloxane of formula II

 

where the molecular weight of reactant II is about 3500 to 4000;

q is about 5 to about 9;

p is about 40 to about 50, and each R2 is independently an alkyl of 1-3 carbon atoms;

said polymerization product being polymerized in the presence of a medium selected from the group consisting of hydrocarbon oils, and mixtures thereof, and

(C) said medium

wherein said polymerization reaction is permitted to take place in a manner in which a substantial portion of the reaction mass is not subject to substantial shearing forces.

34. The silicone gel of claim 32 wherein said polymerization reaction is permitted to take place in the substantial absence of shearing forces.

33. A method of making a clear silicone gel comprising

(A) polymerizing in the presence of a hydrosilylation polymerization catalyst and a medium selected from the group consisting of hydrocarbon oils, and mixtures thereof

(1) (a) an α

,ω

-di lower alkenyl terminated polyorganosiloxafle of formula I

 

having a molecular weight of about 20,000 to about 25,000 with n being about 265 to about 340 and each R1 being independently H, or an alkyl group of 1 or 3 carbons and

(b) optionally an α

,ω

-di ethylene terminated polydiphenyldimethylorganosiloxane; and

(2) a polyorganohydrosiloxane of formula II

 

where the molecular weight of reactant II is about 3500 to 4000;

q is about 5 to about 9;

p is about 40 to about 50; and

each R2 is independently an alkyl having 1-3 carbon atoms resulting in a swollen gel;

(B) milling said swollen gel; and

(C) optionally diluting the result of step (B) with a diluent selected from the group consisting of low viscosity silicone oils, hydrocarbon oils, and lower alkanols;

wherein said polymerization reaction is pennitted to take place in a manner in which a substantial portion of the reaction mass is not subject to substantial shearing forces.

35. The method of claim 33 wherein said polymerization reaction is permitted to take place in the substantial absence of shearing forces.

36. A cross-linked silicone gel substantially free of SiO₂ groups, substantially free of SiO_1.5 groups, and substantially free of polyalkyleneoxide groups, comprising a cross-linked polymerization product of

(A) (1) an α

,ω

-di lower alkenyl terminated polyorganosiloxane of formula I

 

having a molecular weight of about 20,000 to about 25,000 with n being about 265 to about 340 and each R1 being independently H, or an alkyl group of 1 or 3 carbons;

(2) a member selected from the group consisting of mono-α

-olefin, a polyalkoxylated mono-α

-olefin, hydroxyl-terminated-α

-olefin, and mixtures thereof; and

(3) optionally an α

,ω

-di ethylene terminated polydiphenyldimethylorganosiloxane and

(B) a polyorganohydrosiloxane of formula II

 

where the molecular weight of reactant II is about 3500 to 4000;

q is about 5 to about 9;

p is about 40 to about 50, and each R2 is independently an alkyl of 1-3 carbon atoms;

said polymerization product being polymerized in the presence of a medium selected from the group consisting of low viscosity silicone oils;

hydrocarbon oils, and mixtures thereof; and

(C) said medium

wherein (1) said polymerization takes place initially with mixing and said mixing is halted when gelling is visibly seen or (2) said polymerization reaction is permitted to take place in a manner in which a substantial portion of the reaction mass is not subject to substantial shearing forces.

37. The silicone gel of claim 36 which is further diluted with a diluent selected from the group consisting of low viscosity silicone oils, hydrocarbon oils, lower alkanols, and mixtures thereof.

38. A cosmetic formulation comprising about 65% to about 99.9% of the silicone gel of claim 36 about 0.1% to about 30% of at least one cosmetically acceptable ingredient which cosmetic ingredient is not a low viscosity silicone oil, a hydrocarbon oil, or a lower alkanol, or mixtures thereof;

and up to about 10% of a diluent selected from the group consisting of low viscosity silicone oils, hydrocarbon oils, and lower alkanols.

39. A method of making a clear silicone gel comprising

(A) polymerizing in the presence of a hydrosilylation polymerization catalyst and a medium selected from the group consisting of low viscosity silicone oil, hydrocarbon oil, and mixtures thereof

(1) (a) an α

,ω

-di lower alkenyl terminated polyorganosiloxane of formula I

 

having a molecular weight of about 20,000 to about 25,000 with n being about 265 to about 340 and each R 1 being independently H, or an alkyl group of 1 or 3 carbons;

(b) a member selected from the group consisting of mono-α

-olefin, a polyalkoxylated mono-α

-olefin, hydroxyl-terminated-α

-olefin, and mixtures thereof; and

(c) optionally an α

,ω

-di ethylene terminated polydiphenyldimethylorganosiloxane and

(2) a polyorganohydrosiloxane of formula II

 

where the molecular weight of reactant II is about 3500 to 4000;

q is about 5 to about 9;

p is about 40 to about 50; and

each R2 is independently an alkyl having 1-3 carbon atoms resulting in the swollen gel of claim 38;

(B) milling said swollen gel; and

(C) optionally diluting the result of step (B) with a diluent selected from the group consisting of low viscosity silicone oils, hydrocarbon oils, and lower alkanols;

wherein (1) said polymerization takes place initially with mixing and said mixing is halted when gelling is visibly seen or (2) said polymerization reaction is permitted to take place in a manner in which a substantial portion of the reaction mass is not subject to substantial shearing forces.

40. The process of claim 39 further comprising adjusting the viscosity of gel by diluting said gel with a diluent selected from the group consisting of low viscosity silicone oils, hydrocarbon oils, and lower alkanols to result in a diluted gel.

41. The silicone gel resulting from the process of claim 39.

42. The silicone gel resulting from the process of claim 40.

43. A cosmetic composition incorporating said silicone gel of claim 36.

44. A cosmetic composition incorporating the silicone gel resulting from the process of claim 39.

45. A cosmetic composition incorporating the silicone gel resulting from the process of claim 40.

46. The silicone gel of claim 36 which is substantially clear.

47. A method of use of the silicone gel of claim 36 comprising applying said gel to a rubber or rubber-like surface.

48. A composition comprising the silicone gel of claim 36 along with components suitable for application to rubber or rubber-like surfaces.