Examples of 'trimethoxysilane' in a sentence
Meaning of "trimethoxysilane"
trimethoxysilane: A chemical compound with the formula C3H10O3Si, commonly used in the synthesis of silicon-based materials. This term is used in the context of chemistry and materials science
Show more definitions
- The simple siloxane SiH(OCH₃)₃
How to use "trimethoxysilane" in a sentence
Basic
Advanced
trimethoxysilane
A most preferred primer is a trimethoxysilane containing resin.
An example acidic catalyzed silica is glycidoxypropyl trimethoxysilane.
Trimethoxysilane substantially prevented polymerization activity.
The most preferred silane is vinyl trimethoxysilane.
Trimethoxysilane is removed in the heavies stream.
The heavies stream contains trimethoxysilane and small amounts of tetramethoxysilane.
Trimethoxysilane and triethoxysilane are preferred.
Among preferred mercaptosilanes are mercapto propyl trimethoxysilane and mercapto propyl methyl dimethoxy silane.
Vinyl trimethoxysilane represents the particularly preferred silane for use with the fluorocarbon polymer.
A method according to any preceding Claim further characterised in that the alkoxysilane is methyl trimethoxysilane.
Aminopropyl trimethoxysilane is especially preferred.
Said monomer comprises a vinyl group such as trimethoxysilane vinyl ;.
Dimethylsilane, diethylsilane, trimethoxysilane or triethoxysilane can be cited as examples.
A preferred organoalkoxysilane for producing hybrid polymers is y-methacryloxypropyl trimethoxysilane.
Among these, vinyl trimethoxysilane or vinyl triethoxysilane is preferably used.
See also
A radial polymer as claimed in claim 1, wherein the trialkoxysilane is trimethoxysilane.
Preferred silane groups are trimethoxysilane groups, dimethoxymethylsilane groups or triethoxysilane groups.
More specific examples include dimethylsilane, diethylsilane, trimethoxysilane and triethoxysilane.
Reaction with aminopropyl trimethoxysilane would allow for moisture-curable materials.
A method according to claim 1 or claim 2 in which the silane is methyl trimethoxysilane.
However, for many subsequent applications using trimethoxysilane this additional refinement is not required.
A suitable coupling agent when silicaceous fillers are employed is - methacryloxypropyl trimethoxysilane.
Preferably, in this case, use will be made of a trimethoxysilane or trichlorosilane group.
The composition contains a sol-gel component and a reactive monomer including methacryloxypropyl trimethoxysilane.
Examples of such ethylenically unsaturated alkoxysilanes are vinyl trimethoxysilane, allyl trimethoxysilane and methylvinyl dimethoxysilane.
Preferably the organo-silicon compound used as external donor is n-propyl trimethoxysilane.
As the KEMAMINE ® level is dropped the ratio of trimethoxysilane to tetramethoxysilane has increased.
Examples of the vinyl-based compound include vinyl triethoxysilane and vinyl trimethoxysilane.
Example 6 Tridecafluorooctyl triethoxysilane and hexadecyl trimethoxysilane having varying weight ratios are mixed together.
Preferred examples are the corresponding trimethoxy - and triethoxysilane compounds, in particular the trimethoxysilane compounds.
Reactivity Profile Trimethoxysilane may accumulate static electricity ; hazardous polymerization may occur.
The method of claim 9 wherein the primer coating contains trimethoxysilane groups.
Among them, 3-mercaptopropyl trimethoxysilane and the like are preferable.
A further category of suitable coupling agents includes multifunctional coupling agents such as gamma-glycidoxypropyl trimethoxysilane.
Among them, 3-methacryloyloxypropyl trimethoxysilane is preferable.
Specific examples of these compounds include glycidyl methacrylate, glycidyl acrylate and Y-methacryloyloxypropyl trimethoxysilane.
Among them, 3-glycidoxypropyl trimethoxysilane and 3-glycidoxypropyl triethoxysilane are particularly preferable.
Another source material for hydrophobic coatings is an alkyl trimethoxysilane of the formula,.
Then 64 grams of vinyl trimethoxysilane was added to the reaction mixture over 5 minutes.
Moisture scavengers such as molecular sieves, oxazolidines and / or vinyl trimethoxysilane are often employed.
A process for producing trimethoxysilane according to Claim 1 comprising,.
A method as in claim 11, wherein said composition comprises a mixture of methyl trimethoxysilane and tetraethyl orthosilicate.
Of these compounds, vinyl trimethoxysilane, vinyl triethoxysilane, and Y-methacryloxypropyl trimethoxysilane are specifically preferred.
More particularly, a suitable group may be an alkoxysilane group, such as a trimethoxysilane group, a triethoxysilane group.
Next, 5.5g of vinyl trimethoxysilane was added as a moisture scavenger.
Particularly suitable examples include methyl cyclohexyl dimethoxysilane, isobutyl trimethoxysilane and diphenyl dimethoxysilane.
For comparison, 3-acryloylpropyl trimethoxysilane ( AcHA ) was also grafted to SiHA using the same procedure.
Other activated silanes for this purpose include triethoxysilane, trichlorosilane, trimethoxysilane or other trialkoxysilanes.
Examples of the chloro-based compound include 3-chloropropyl trimethoxysilane, 3-chloropropyl triethoxysilane, 2-chloroethyl trimethoxysilane and 2-chloroethyl triethoxysilane.
Another preferred organoalkoxysilane is Y-glycidoxypropyl trimethoxysilane.
