Sulfur-containing polyorganosiloxane compositions and related aspects

Patent metadata

Field	Value
Publication number	US-10351704-B2
Application number	US-201515518332-A
Country	US
Kind code	B2
Filing date	Nov 6, 2015
Priority date	Nov 13, 2014
Publication date	Jul 16, 2019
Grant date	Jul 16, 2019

Abstract

Described are hydrosilylation-curable polyorganosiloxane compositions containing sulfur, including hydrosilylation-curable polyorganosiloxane prepolymers and hydrosilylation-cured polyorganosiloxane polymer products made therefrom, as well as methods of preparing and using the same, devices comprising or prepared from the same, and sulfur-functional organosiloxanes useful therein.

First claim

What is claimed is:

1. A degradation-inhibited hydrosilylation-curable composition comprising the following constituents:
(i) a hydrosilylation-curable polyorganosiloxane prepolymer,
(ii) a metal component of a hydrosilylation catalyst, and
(iii) a sulfur compound having a boiling point greater than 150 degrees Celsius (° C.);
wherein the atomic amount, in moles, of sulfur atoms of the sulfur compound is from 5 to 10,000 times greater than the atomic amount, in moles, of (ii) the metal component of a hydrosilylation catalyst; and
wherein the composition either has the hydrosilylation-curable polyorganosiloxane prepolymer, as described below, for constituent (i-a) or the composition has the sulfur compound, as described below, for constituent (iii-a) or the composition has both constituents (i-a) and (iii-a):
(i-a) the hydrosilylation-curable polyorganosiloxane prepolymer is a hydrosilylation-curable resin-linear organosiloxane block copolymer comprising:
40 to 90 mole percent D-type units of the formula [R 1 2 SiO 2/2 ],
10 to 60 mole percent T-type units of the formula [R 2 SiO 3/2 ],
0.5 to 35 mole percent silanol groups [Si—OH];
wherein each R 1 and R 2 independently is a (C 1 -C 30 )hydrocarbyl that has 0 aliphatic unsaturated bond or a (C 1 -C 30 )hydrocarbyl which comprises at least 1 aliphatic unsaturated bond, wherein the hydrosilylation-curable resin-linear organosiloxane block copolymer comprises from 0.5 to 5 mole percent of the (C 1 -C 30 )hydrocarbyl comprising at least one aliphatic unsaturated bond;
wherein the D-type units [R 1 2 SiO 2/2 ] are arranged in linear blocks having an average of from 100 to 300 D-type units [R 1 2 SiO 2/2 ] per linear block and the T-type units [R 2 SiO 3/2 ] are arranged in non-linear blocks having a molecular weight of at least 500 grams per mole (g/mol), wherein at least 30 mole percent of the non-linear blocks are crosslinked with each other and wherein each linear block is linked to at least one non-linear block via a divalent linker comprising a D-type or T-type siloxane unit; and
wherein the hydrosilylation-curable resin-linear organosiloxane block copolymer has a weight average molecular weight (Mw) of at least 20,000 g/mol; or
(iii-a) the sulfur compound is a sulfur-functional organosiloxane of formula (I): (R 3 R 4 R 5 SiO 1/2 ) a1 (R 3 R 4 SiO 2/2 ) b1 (R 3 SiO 3/2 ) c1 (O 3/2 Si—R 6 —S—(S) m —R 7 —SiO 3/2 ) d1 (SiO 4/2 ) e1 (I), wherein subscript m is 0, 1, 2, or 3; subscripts a1+b1+c1+d1+e1=1, a1 is from 0 to 0.5, b1 is from 0 to <1, c1 is from 0 to 1, d1 is from 0 to 1, and e1 is from 0 to 0.2;
wherein each of R 3 , R 4 , and R 5 independently is a (C 1 -C 30 )hydrocarbyl, a mercapto-functional ((HS)-functional) (C 1 -C 30 )hydrocarbyl, or a (C 1 -C 30 )heterohydrocarbyl containing a sulfide group, a disulfide group, a trisulfide group, or a tetrasulfide group; and
wherein each of R 6 and R 7 independently is a bond, a (C 1 -C 30 )hydrocarbylene, or a (C 1 -C 30 )heterohydrocarbylene containing a sulfide group, a disulfide group, a trisulfide group, or a tetrasulfide group; and
with the proviso that d1 is >0 or at least one of R 3 , R 4 , and R 5 independently is a mercapto-functional (C 1 -C 30 )hydrocarbyl or a (C 1 -C 30 )heterohydrocarbyl containing a sulfide group, a disulfide group, a trisulfide group, or a tetrasulfide group.

2. The composition of claim 1 wherein the composition has the hydrosilylation-curable polyorganosiloxane prepolymer described as constituent (i-a); wherein the hydrosilylation-curable resin-linear organosiloxane block copolymer comprises 1 to 35 mole percent silanol groups; or the hydrosilylation-curable resin-linear organosiloxane block copolymer comprises 12 to 22 mole percent silanol groups; or the hydrosilylation-curable resin-linear organosiloxane block copolymer has a M w of 40,000 g/mol to 250,000 g/mol; or the hydrosilylation-curable resin-linear organosiloxane block copolymer comprises 30 to 60 mole percent T-type units of the formula [R 2 SiO 3/2 ]; or the hydrosilylation-curable resin-linear organosiloxane block copolymer comprises from 0.5 to 4.5 mole percent of the (C 1 -C 30 )hydrocarbyl comprising at least one aliphatic unsaturated bond; or the hydrosilylation-curable resin-linear organosiloxane block copolymer comprises 12 to 22 mole percent silanol groups; the hydrosilylation-curable resin-linear organosiloxane block copolymer has a Mw of 40,000 g/mol to 250,000 g/mol; the hydrosilylation-curable resin-linear organosiloxane block copolymer comprises 30 to 60 mole percent T-type units of the formula [R 2 SiO 3/2 ]; and the hydrosilylation-curable resin-linear organosiloxane block copolymer comprises from 0.5 to 4.5 mole percent of the (C 1 -C 30 )hydrocarbyl comprising at least one aliphatic unsaturated bond.

3. The composition of claim 2 wherein the sulfur compound is a diorgano polysulfide of formula (II): R a —S—(S) n —R b (II), wherein subscript n is 1, 2, or 3, each of R a and R b independently is an unsubstituted (C 2 -C 30 )hydrocarbyl or a (C 1 -C 30 )hydrocarbyl substituted with 1 or more substituents R C , wherein each R C independently is halogen, —NH 2 , —NHR, —NR 2 , —NO 2 , —OH, —OR, oxo (═O), —C≡N, —C(═O)—R, —OC(═O)R, —C(═O)OH, —C(═O)OR, —SH, —SR, —SSH, —SSR, —SC(═O)R, —SO 2 R, —OSO 2 R, —SiR 3 , or —Si(OR) 3 ; wherein each R independently is an unsubstituted (C 1 -C 30 )hydrocarbyl.

4. The composition of claim 1 wherein the composition has the sulfur compound described as constituent (iii-a); wherein the sulfur compound is a sulfur-functional organosiloxane of formula (I-a): (R 3 R 4 SiO 2/2 ) b (O 3/2 Si—R 6 —S—(S) m —R 7 —SiO 3/2 ) d (I a), wherein b is from <1.00 to 0.80, d is from >0 to 0.20, each R 3 independently is (C 1 -C 6 )alkyl, and each R 4 independently is a (C 1 -C 6 )alkyl, phenyl, (C 2 -C 6 )alkenyl, or (C 2 -C 6 )alkynyl; m is 0, 1, 2, or 3; and each of R 6 and R 7 independently is a bond or a (C 1 -C 10 )hydrocarbylene.

5. The composition of claim 4 wherein in formula (I-a) each R 3 independently is (C 1 -C 3 )alkyl and each R 4 independently is (C 1 -C 3 )alkyl or phenyl, with the proviso that on average, per molecule, at least one R 4 is phenyl; or in formula (I-a) m is 1; and each of R 6 and R 7 is a bond; or in formula (I-a) each R 3 independently is (C 1 -C 3 )alkyl and each R 4 independently is (C 1 -C 3 )alkyl or phenyl, with the proviso that on average, per molecule, at least one R 4 is phenyl; m is 1; and each of R 6 and R 7 is a bond.

6. The composition of claim 1 , wherein when the composition has constituent (i-a), the sulfur compound is dihexyl disulfide; dioctadecyl disulfide; dioctadecyl trisulfide; dioctadecyl tetrasulfide; bis(2-butoxy-ethyl) disulfide; or 1 docosanethiol, or a combination of any two or more thereof; and when the composition has constituent (iii-a), the sulfur compound is a sulfur-functional organosiloxane of formula (T C3H6S— ) 0.090 T Ph 0.910 .

7. The composition of claim 1 wherein: (a) the atomic amount of (ii) the metal component of a hydrosilylation catalyst is from greater than 0 to 100 ppm; or (b) (ii) the metal component of a hydrosilylation catalyst is palladium, platinum, rhodium, ruthenium, or a combination of any two or more thereof; or (c) (ii) the metal component of a hydrosilylation catalyst is platinum or rhodium; or (d) (ii) the metal component of a hydrosilylation catalyst is platinum, and the atomic amount of platinum is from 0.1 to 5 ppm of the composition.

8. The composition of claim 1 being substantially solvent free.

9. An optical and/or electronic device comprising the composition of claim 1 or a hydrosilylation cured product made therefrom.

10. A thermally aged hydrosilylation-cured p

Assignees

• Dow Corning

Inventors

• Nishida Fumito
• Swier Steven
• Wei Yanhu

Classifications

• C08L83/10

  Block- or graft-copolymers containing polysiloxane sequences (obtained by polymerising a compound having a carbon-to-carbon double bond on to a polysiloxane C08L51/08, C08L53/00) · CPC title

• C08L83/08 Primary

  containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen · CPC title

• C08L83/00

  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 title

• C08K5/36 Primary

  Sulfur-, selenium-, or tellurium-containing compounds {(C08K5/0091 takes precedence)} · CPC title

• C08G77/28

  sulfur-containing groups · CPC title