Curable organosiloxane oligomer compositions

• US 10,370,499 B2
• Filed: 12/22/2014
• Issued: 08/06/2019
• Est. Priority Date: 12/31/2013
• Status: Active Grant

• Current Assignee: 3M Innovative Properties Company (3M Company)
• Original Assignee: 3M Innovative Properties Company (3M Company)
• Inventors: Kumar, Kanta, Wolter, James T.
• Primary Examiner(s): Peng, Kuo Liang
• Application Number:
  US15/108,827
• Publication Number:
  US 20160319081A1
• Time in Patent Office: 1,688 Days
• CPC Class Codes: C08G 77/08 characterised by the catalysts used
• CPC Class Codes: C08G 77/24 halogen-containing groups
• CPC Class Codes: C08G 77/44 containing only polysiloxane sequences
• CPC Class Codes: C08K 5/31 Guanidine; Derivatives thereof
• CPC Class Codes: C08K 5/5399 Phosphorus bound to nitrogen
• 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 83/08 containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
• CPC Class Codes: C09D 183/10 Block or graft copolymers containing polysiloxane sequences obtained by polymerising a compound having a carbon-to-carbon double bond on to a polysiloxane C09D151/08, C09D153/00
• CPC Class Codes: C09J 2301/302 the adhesive being pressure-sensitive, i.e. tacky at temperatures inferior to 30°C
• CPC Class Codes: C09J 2483/005 in the release coating
• CPC Class Codes: C09J 7/401 characterised by the release coating composition

Abstract

A curable composition including (a) at least one organosiloxane compound, fluorinated organosiloxane compound, or combination thereof having reactive silane functionality including at least two hydroxysilyl moieties; (b) at least one organosiloxane oligomer, fluorinated organosiloxane oligomer, or combination thereof having reactive silane functionality including at least two hydrosilyl moieties; and (c) a catalyst composition including (1) at least one base selected from amidines, guanidines, phosphazenes, proazaphosphatranes, and combinations thereof, and (2) at least one Lewis acid. At least one of the components (a) and (b) has an average reactive silane functionality of at least three, and the composition is substantially free of organic solvent(s). An alkoxysilane compound may be optionally included in the curable composition. A process for coating the composition to prepare articles having the cross-linked composition on at least a portion of at least one major substrate surface is also disclosed.

Claims

1. A composition comprising the following components:

(a) at least one organosiloxane compound, fluorinated organosiloxane compound, or a combination thereof, comprising reactive silane functionality comprising at least two hydroxysilyl moieties;

(b) at least one organosiloxane oligomer, fluorinated organosiloxane oligomer, or a combination thereof, comprising reactive silane functionality comprising at least two hydrosilyl moieties; and

(c) a catalyst composition comprising (1) at least one base selected from amidines, guanidines, phosphazenes, proazaphosphatranes, and combinations thereof, and (2) at least one Lewis acid;

wherein at least one of said components (a) and (b) has an average reactive silane functionality of at least three, the composition is substantially free of an organic solvent, and the composition further comprises

(R″

O)_p—

Si(R′

)_3-p[G-Si(R′

)₂]_t—

(W)_s—

[(R′

)₂SiO]_q—

[Si(R′

)₂-G]_t—

Si(R′

)_3-p—

(OR″

)_p;

wherein;

G and W are oxy;

each R′

is independently selected from alkyl, alkylene, fluoroalkyl, aryl, fluoroaryl, cycloalkyl, fluorocycloalkyl, hetroalkyl, hetrofluoroalkyl, hetroaryl, hetrofluoroaryl, hetrocycloalkyl, hetrofluorocycloalkyl, oxyalkyl, oxyfluoroalkyl, oxyaryl, oxyfluoroaryl, oxycycloalkyl, oxyfluorocycloalkyl, oxyhetroalkyl, oxyhetrofluoroalkyl, oxyhetroaryl, oxyhetrofluoroaryl, oxyhetrocycloalkyl, and oxyhetrofluorocycloalkyl;

each R″

is independently selected from alkyl;

P is an integer selected from 1, 2 or 3;

each q is independently selected as an integer of 0-150, inclusive;

s is selected as an integer of 0-40, inclusive; and

each t is independently selected as an integer of 0 or 1.

2. The composition of claim 1, wherein said components (a) and (b) each comprise an organosiloxane oligomer having a weight average molecular weight no greater than 5,000 Da, optionally wherein each organosiloxane oligomer is a dimethylsiloxane oligomer.

3. The composition of claim 1, wherein said component (a) is hydroxyl-endblocked.

4. The composition of claim 1, wherein said component (a) is represented by:

(HO)_p—

Si(R′

)_3-p—

[G-Si(R′

)₂]_t—

O—

[(R′

)₂SiO]_q—

[Si(R′

)₂-G]_t—

Si(R′

)_3-p—

(OH)_p

wherein each G is independently a divalent linking group;

each R′

is independently selected from alkyl, fluoroalkyl, aryl, fluoroaryl, cycloalkyl, fluorocycloalkyl, heteroalkyl, heterofluoroalkyl, heteroaryl, heterofluoroaryl, heterocycloalkyl, heterofluorocycloalkyl;

each p is independently an integer of 1, 2, or 3;

q is an integer of 0 to 150; and

each t is independently an integer of 0 or 1.

5. The composition of claim 1, wherein said component (a) comprises a mixture of (1) at least one polyorganosiloxane, fluorinated polyorganosiloxane, or combination thereof having a weight average molecular weight in the range of 10,000 to 1,000,000 and (2) at least one organosiloxane oligomer, fluorinated organosiloxane oligomer, or combination thereof having a weight average molecular weight in the range of about 150 to about 5,000 Da.

6. The composition of claim 1, wherein said component (b) is represented by the following general formula:

R′

₂R″

SiO(R′

₂SiO)_r(HR′

SiO)_sSiR″

R′

₂

wherein each R′

is independently selected from H, alkyl, alkenyl, fluoroalkyl, aryl, fluoroaryl, cycloalkyl, fluorocycloalkyl, heteroalkyl, heterofluoroalkyl, heteroaryl, heterofluoroaryl, heterocycloalkyl, heterofluorocycloalkyl;

each R″

is independently H or R′

;

r is an integer of 0 to 150, inclusive; and

s is an integer of 2 to 150, inclusive.

7. The composition of claim 1, wherein the base of component (c) is selected from:

(1) amidine compounds that are represented by the following general formula;

8. The composition of claim 7, wherein the base is selected to include at least two amidine compounds, guanidine compounds, phosphazene compounds, or combinations thereof, and further wherein any two or more of R1, R2, R3, R4, R5, R6, and R7 of said at least two amidine, guanidine, and phosphazene compounds are bonded together to form at least one ring structure.

9. The composition of claim 1, wherein said Lewis acid is selected from metal salts, trialkylborates, triarylborates, and combinations thereof.

10. The composition of claim 1, further comprising at least one carboxylic acid, at least one carboxylic acid anhydride, or a combination thereof.

11. The composition of claim 1, wherein said composition is substantially free of a tin catalyst.

12. The composition of claim 1 wherein the catalyst composition (1) comprises at least one base selected from 1,2-dimethyl-1,4,5,6-tetrahydropyrimidine, 1,8-diazabicyclo[5.4.0]-7-undecene (DBU), 1,5-diazabicyclo[4.3.0]-5-nonene (DBN), 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD), 7-methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (MTBD), 2-tert-butyl-1,1,3,3-tetramethylguanidine, and combinations thereof.

13. The composition of claim 1, wherein at least one of said component (a) or said component (b) is a fluorinated organosiloxane oligomer.

14. The composition of claim 1, wherein said Lewis acid is a zinc(II) salt that is used in a 1:

1 molar ratio with said base.

15. A process comprising

(a) applying the composition according to claim 1 to at least a portion of a substrate;

and

(b) at least partially curing said composition to form a cross-linked coating on the substrate.

16. An article comprising the cross-linked coating prepared by the process of claim 15, wherein the at least a portion of the substrate is at least one major surface of the substrate, optionally wherein the cross-linked coating contacts the at least one major surface of the substrate.

17. The article of claim 16, wherein said article further comprises a layer of a pressure-sensitive adhesive prepared by application of a photopolymerizable composition to said cross-linked coating, followed by irradiation of said photopolymerizable composition to effect photopolymerization thereof.