IP Library Granted Patent US 9,334,435
Granted Patent B2
US 9,334,435 · App. 14/443,325 · Granted May 10, 2016

Abradable silicone elastomer compound and use thereof

Inventor: Andreas Koellnberger (Kirchdorf, DE)
Assignee: WACKER CHEMIE AG
C09J183/04C08G77/12C08L83/04G02B1/04H01L24/01
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,334,435
App. No.
14/443,325
Granted
May 10, 2016
Kind
B2
Abstract

Addition curing silicone elastomers of high Shore D hardness are grindable and polishable, and are particularly useful as temporary adhesives in the processing of semiconductor wafers.

Claims (20)

1. An addition-crosslinkable silicone elastomer composition comprising:

(A1) 1-10% by weight of at least one linear organopolysiloxane containing at least 2 SiC-bonded radicals having aliphatic carbon-carbon multiple bonds, wherein the mean molar mass of (A1) is not more than 15,000 g/mol,

(A2) 1-20% by weight of at least one linear organopolysiloxane containing at least 2 SiC-bonded radicals having aliphatic carbon-carbon multiple bonds, wherein the mean molar mass of (A2) is at least 40,000 g/mol,

(B) 1-40% by weight of at least one organopolysiloxane containing at least three Si-bonded hydrogen atoms per molecule, having a content of Si-bonded hydrogen of from 0.04 to 1.7% by weight and a mean molar mass of not more than 20,000 g/mol,

(D) 1-100 ppm (based on the metal) of a hydrosilylation catalyst,

(E) 50-99% by weight of at least one branched silicone resin of the general empirical formula (I)

(R 3 3 SiO 1/2 ) l (R 4 R 3 2 SiO 1/2 ) t (R 4 R 3 SiO) u (R 3 2 SiO) p (R 4 SiO 3/2 ) q (R 3 SiO 3/2 ) r (SiO 4/2 ) s   (I),

wherein

R 3 denotes a linear aliphatic radical,

R 4 denotes an aliphatically unsaturated radical having a terminal C═C double bond,

l, t, u, p, q, r and s denote integers,

wherein the following apply:

l≧0, t≧0, u≧0, p≧0, q≧0, r≧0 and s≧0; and

the content of aliphatically unsaturated groups in (E) is between 0.2 and 10 mmol/g; and

(E) has a mean molar mass of not more than 10 5 g/mol,

with the proviso that the ratio of the Si—H groups provided by component (B) to the aliphatically unsaturated groups provided by components (A1), (A2) and (E) is between 0.5 and 5 and the ratio of the dynamic viscosity of the silicone elastomer composition at shear rates of 1 s −1 and 100 s −1 and a temperature of 20° C. is not more than 1.2 and after crosslinking exhibits a Shore D hardness of at least 25.

2. A process for the preparation of a silicone elastomer compositions of claim 1 , wherein all the components are mixed together.

3. A molding, adhesive bond or optical component, comprising a cured silicone elastomer of claim 1 .

4. The adhesive bond of claim 3 , which is a temporary adhesive bond.

5. In the processing of a semiconductor wafer wherein an adhesive is used to bond the wafer to a substrate in temporary fashion, the improvement comprising employing an adhesive which is a curable silicone elastomer composition of claim 1 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2019
From: WACKER CHEMIE AG
To: NISSAN CHEMICAL CORPORATION
Reel/Frame 049834/0681 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2015
From: KÖLLNBERGER, ANDREAS
To: WACKER CHEMIE AG
Reel/Frame 035739/0369 →
Priority Claims (1)
DE 10 2012 220 954 · Nov 16, 2012 · national
Continuity (1)
Related Publication 20150299533A1 · Oct 22, 2015