EP0802222A1

Method of adhesion improvement for silicone compositions

Abstract

A method is disclosed for adhesion improvement of a room temperature vulcanizable (RTV) silicone composition to substrates. This is accomplished by adding a monoketoester, such as ethylacetoacetate, to an RTV silicone composition which is comprised of an alkoxy ended polydiorganosiloxane, a crosslinker having silicon-bonded methoxy or ethoxy group, a filler and a titanate catalyst. Then by applying this composition to a substrate to form intimate contact between the substrate and uncured composition. Thereafter, the composition is exposed to atmospheric moisture for a sufficient time to obtain a cured material. When tested, the bond between the cured material and the substrate surprisingly exhibits cohesive failure.

EP0802222A1, drawing sheet 1
Sheet 1 of 11

Term

Term ended

Projected expiry passed 11 April 2017, 9.5 years ago.

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10 claims: 5 independent, 5 dependent

  1. 1
    A method of improving the adhesion of a room temperature vulcanizable silicone composition to substrates comprising (I) adding a monoketoester to a room temperature vulcanizable silicone composition comprising a polydiorganosiloxane having endgroups containing for each terminal silicon atom at least two silicon-bonded methoxy, ethoxy, propoxy or butoxy groups;a crosslinker having at least two silicon-bonded methoxy or ethoxy groups per molecule;filler;and titanium catalyst;characterized by the presence of 0.25 to 3 moles of monoketoester per one mole of titanium atom in the titanium catalyst;(II) applying the resulting silicone composition from (I) to a substrate surface, (III) exposing the silicone composition to atmospheric moisture for a sufficient time to obtain a cured material bonded to the substrate.
  2. 2
    The method in accordance with claim 1 in which the silicone composition has as the polydiorganosiloxane, a polydiorganosiloxane of the formula where R 1 is methyl or ethyl; R 2 is methyl, ethyl, vinyl, or phenyl; R 3 is methyl, ethyl, or phenyl; n is 2 or 3:p is at least 200;and Z is selected from a divalent hydrocarbon radical free of aliphatic unsaturation of 2 to 18 carbon atoms or a divalent group of the general formula where R 3 is defined above, G is a divalent hydrocarbon radical free of aliphatic unsaturation of 2 to 18 carbon atoms, and c is from 1 to 6 inclusive.
  3. 4
    The method in accordance with any of claims 1 to 3 in which the crosslinker is selected from dimethyldimethoxysilane or methyltrimethoxysilane.
  4. 5
    The method in accordance with any of claims 1 to 4 in which the titanium catalyst is a tetraalkyl titanate of the formula Ti(OR) 4 where R is ethyl, propyl, butyl or amyl.
  5. 6
    The method in accordance with any of claims 1 to 4 in which the titanium catalyst is dialkoxy-bis-ethylacetoacetate titanium and the ethylacetoacetate ligand of said titanium catalyst is at least a portion of the required monoketoester.
  6. 7
    The method in accordance with claim 6 in which the alkoxy group in the dialkoxy-bis-ethylacetoacetate titanium is isopropoxy.
  7. 8
    The method in accordance with any of claims 1 to 7 in which the substrate is a plastic or metal substrate.
  8. 9
    The method in accordance with claim 8 in which the plastic substrate is acrylic.
  9. 10
    The method in accordance with claim 8 in which the metal substrate is anodized aluminum.