US2020331767A1PendingUtilityA1
Method for producing aerogels
Est. expiryOct 2, 2034(~8.2 yrs left)· nominal 20-yr term from priority
G02F 1/133634C01B 33/1546C01B 33/1585C01B 33/16C01B 33/1435G02F 1/133502
46
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Claims
Abstract
The invention relates to a method for producing aerogels, in particular silica aerogels, by way of a sol-gel process.
Claims
exact text as granted — not AI-modified1 . A hydrophobic silica aerogel,
characterized in that the aerogel has absolute sizes of 0.01 to 10 mm for a particle, has a bulk density of 0.05 to 0.30 g/cm 3 and has a contact angle with water of 130 to 165°.
2 . The hydrophobic silica aerogel according to claim 1 , characterized in that the aerogel has absolute sizes of 0.1 to 8 mm for a particle.
3 . The hydrophobic silica aerogel according to claim 1 , characterized in that the aerogel has a bulk density of 0.08 to 0.25 g/cm 3 .
4 . The hydrophobic silica aerogel according to claim 1 , characterized in that the aerogel has an average pore diameter of less than 300 nm.
5 . The hydrophobic silica aerogel according to claim 1 , characterized in that the aerogel has a contact angle with water of 140 to 165°.
6 . The hydrophobic silica aerogel according to claim 1 , characterized in that the aerogel is produced via a sol-gel process.
7 . The hydrophobic silica aerogel according to claim 6 , characterized in that the sol-gel process involves an in situ hydrophobicization of the gel carried out as it is formed.
8 . The method as claimed in claim 6 , characterized in that the gel is formed in the presence of at least one hydrophobicizing agent.
9 . The method as claimed in claim 8 , characterized in that the hydrophocizing agent is selected from the group consisting of phosphonates, sulfonates, substituted amines, silanes, polysiloxanes, siliconates, carboxylic acid derivatives, ethoxylates, polyethers, and mixtures thereof.
10 . The method as claimed in claim 9 , characterized in that the method utilizes a polysiloxane having reactive functional groups.
11 . The method as claimed in claim 10 , characterized in that the method utilizes a polysiloxane having reactive functional entities selected from the group consisting of hydroxyl groups, amine groups and carboxyl groups.
12 . The method as claimed in claim 10 , characterized in that the method utilizes a polysiloxane having a weight-average molar mass M w in the range from 250 to 50 000 g/mol.
13 . The method as claimed in claim 9 , characterized in that the method utilizes a silane of general formula I
R 1 n SiR 2 4-n (I)
where
n=1 to 3;
R 1 =a substituent selected from the group consisting of C 1 - to C 30 -alkyl and C 6 - to C + -aryl; and
R 2 =a substituent selected from the group consisting of a halide, and OX where X=hydrogen, alkyl, aryl, polyether and a carboxylic acid derivative.
14 . The method as claimed in claim 6 , characterized in that it utilizes a siliconate of general formula II
HO—[Si(R)(OM)—O—] n H (II)
where
n=1 to 6;
R=a substituent selected from the group consisting of C 1 - to C 10 -alkyl and C 6 - to C 15 -aryl; and
M=monovalent metal.
15 . The method as claimed claim 6 , carried out in a medium selected from the group consisting of only one dissolving medium and only one dispersing medium.
16 . The method as claimed in claim 13 , characterized in that the medium selected is a polar medium.
17 . The method as claimed in claim 13 , characterized in that the medium selected is a polar protic medium.
18 . The method as claimed in claim 13 , characterized in that the medium is selected from the group consisting of alcohols, amines and water.
19 . The method as claimed in claim 13 , characterized in that the medium is selected from the group consisting of a C 1 - to C 8 -alcohols.
20 . The method as claimed in claim 12 , characterized in that the medium is selected from the group consisting of methanol, ethanol, propanol and water.Join the waitlist — get patent alerts
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