Oil resistant silicone sealants

• US 6,114,438 A
• Filed: 09/08/1995
• Issued: 09/05/2000
• Est. Priority Date: 09/08/1995
• Status: Expired due to Fees

• Current Assignee: Dow, Inc.
• Original Assignee: Dow, Inc.
• Inventors: Lower, Loren Dale
• Primary Examiner(s): DAWSON, ROBERT A
• Application Number:
  US08/524,661
• Time in Patent Office: 1,824 Days
• Field of Search: 524/731, 524/788, 528/17, 528/33, 528/34, 528/901
• US Class Current: 524/788
• CPC Class Codes: C08G 77/16 to hydroxyl groups
• CPC Class Codes: C08K 3/26 Carbonates; Bicarbonates
• CPC Class Codes: C08L 2666/44 Silicon-containing compounds
• CPC Class Codes: C08L 2666/54 Inorganic substances
• 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
• CPC Class Codes: Y10S 528/901 Room temperature curable silicon-containing polymer

Abstract

An oxime curable silicone sealant composition with good oil resistance can be formulated, using calcium carbonate filler with higher water content than previously known to be useful. The sealant formulation is adjusted to accommodate higher water content by adjusting the ketoximosilane crosslinker level. The correct amount of crosslinker is determined by the hydroxy content present from both the silanol on the base polymer and the water content of the filler.

Claims

1. A room temperature curing silicone sealant composition utilizing high moisture fillers, formed by combining, based on the weight of the silicone sealant composition:

25 to 75% diorganosiloxane base polymer of viscosity 1.0 Pa.s to 300 Pa.s, in which the terminal groups are selected from the group consisting of silanol and triorganosilyl groups, provided that at least 60% of the terminal groups are silanol groups;

0 to 25% triorganosilyl endblocked polydiorganosiloxane fluid of viscosity 0.1 Pa.s to 10 Pa.s;

17 to 65% calcium carbonate filler, where the filler contains greater than 0.25% water by weight;

0.01 to 2% tin catalyst;

0 to 2.0% of an epoxy-functional alkoxysilane; and

an amount of a ketoximosilane of the formula ##STR3## where R¹, R², and R³ are monovalent hydrocarbons which may be the same or different from each other, and a is 0 or 1, and R⁴ is an alkoxy, and b is 0 to 2, inclusive, said amount being calculated so that there are greater than 1.3 moles ketoximosilane per silanol equivalent in the diorganosiloxane base polymer and the calcium carbonate filler.

2. The composition of claim 1 in which the diorganosiloxane base polymer is polydimethylsiloxane of viscosity 10 Pa.s to 20 Pa. s, in which 10 to 20% of the endgroups are capped with triorganosilyl endblocker, and 80 to 90% of the endgroups are silanol.

3. The composition of claim 1 in which the diorganosiloxane plasiticizer is polydimethylsiloxane with viscosity of about 1 to 5 Pa.s.

4. The composition of claim 1 in which the R¹ and R² on the ketoximosilane are methyl, ethyl, amyl or isobutyl.

5. The composition of claim 1 in which R³ on the ketoximosilane is methyl, ethyl, butyl, or vinyl.

6. The composition of claim 1 in which R⁴ is a methoxy group.

7. The composition of claim 1, in which 0.3 to 1.0% of an epoxy-functional alkoxysilane is added.

8. The composition of claim 7 where the epoxy-functional alkoxysilane is gamma-glycidoxypropyl trimethoxysilane.

9. The composition of claim 1 where the calcium carbonate filler of water content greater that 0.25% is a treated precipitated calcium carbonate.

10. The composition of claim 1 where the amount of ketoximosilane is 1.3 to 2.5 moles per mole of total silanol equivalent from the base polymer and the filler.

11. A method of making a room temperature curing silicone sealant composition utilizing high moisture fillers, the method comprising combining, based on the weight of the silicone sealant composition:

25 to 75% diorganosiloxane base polymer of viscosity 1.0 Pa.s to 300 Pa.s, in which the terminal groups are selected from the group consisting of silanol and triorganosilyl groups, provided that at least 60% of the terminal groups are silanol groups;

0 to 25% triorganosilyl endblocked polydiorganosiloxane fluid of viscosity 0.1 Pa.s to 10 Pa.s;

17 to 65% calcium carbonate filler, where the filler contains greater than 0.25% water by weight;

0.01 to 2% tin catalyst;

0 to 2.0% of an epoxy-functional alkoxysilane; and

an amount of a ketoximosilane of the formula ##STR4## where R¹, R²,, and R³ are monovalent hydrocarbons which may be the same or different from each other, and a is 0 or 1, and R⁴ is an alkoxy, and b is 0 to 2, inclusive, said amount being calculated so that there are greater than 1.3 moles ketoximosilane per silanol equivalent in the diorganosiloxane base polymer and the calcium carbonate filler.

12. The method of claim 11 in which the diorganosiloxane base polymer is polydimethylsiloxane of viscosity 10 Pa.s to 20 Pa.s, in which 10 to 20% of the endgroups are capped with triorganosilyl endblocker, and 80 to 90% of the endgroups are silanol.

13. The method of claim 11 in which the diorganosiloxane plasiticizer is polydimethylsiloxane with viscosity of about 1 to 5 Pa.s.

14. The method of claim 11 in which the R¹ and R² on the ketoximosilane are methyl, ethyl, amyl or isobutyl.

15. The method of claim 11 in which R³ on the ketoximosilane is methyl, ethyl, butyl, or vinyl.

16. The method of claim 11 in which R⁴ is a methoxy group.

17. The method of claim 11, in which 0.3 to 1.0% of an epoxy-functional alkoxysilane is added.

18. The method of claim 17 where the epoxy-functional alkoxysilane is gamma-glycidoxypropyl trimethoxysilane.

19. The method of claim 11 where the calcium carbonate filler of water content greater that 0.25% is a treated precipitated calcium carbonate.

20. The method of claim 11 where the amount of ketoximosilane is 1.3 to 2.5 moles per mole of total silanol equivalent from the base polymer and the filler.