Examples of 'monomers containing' in a sentence

Meaning of "monomers containing"

monomers containing: Refers to molecules or compounds that serve as the building blocks for larger polymer structures. This phrase is often used in chemistry or biochemistry contexts to describe smaller molecular units that can undergo polymerization to form larger chains or structures

How to use "monomers containing" in a sentence

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monomers containing
Monomers containing an allyl group are also preferred.
These polymers are made from monomers containing aromatic nuclei.
Monomers containing an allyl group have to be used.
The reactivity can be further influenced by incorporation of monomers containing chlorine or bromine.
Monomers containing acrylic or acrylamide bridges should be avoided.
The polymers may be made only from monomers containing perfluoro alkyl groups.
Monomers containing such associative groups are water insoluble.
Other examples of components of this class are unsaturated monomers containing sulfonic acid groups.
Monomers containing such chain extenders also produce polyureas.
Also included are those polymers which are prepared from monomers containing functional groups.
Multifunctional monomers containing one or more ionic groups may be used.
Hydroxyl functional monomers include ethylenically unsaturated monomers containing one or more hydroxyl groups.
An example are monomers containing one carboxyl group and two hydroxyl groups.
The expression cationic monomers denotes more particularly monomers containing a quaternary ammonium functional group.
Monomers containing unsulfonated aryl groups may also be present in copolymer compositions.

See also

Copolymer comprised of ethylenically unsaturated monomers containing hydroxyl groups and other vinyl monomers.
Preferred monomers containing epoxy groups are glycidyl acrylate and glycidyl methacrylate.
Copolymers or terpolymers may also include monomers containing sulfonic acid groups or salts thereof.
Monomers containing both epoxy and acrylic functionality are categorized herein as acrylate monomers.
Typical addition polymers are formed from monomers containing at least one ethylenically unsaturated bond.
Preferred monomers containing the anhydride functionality are itaconic anhydride and maleic anhydride.
But this invention does not specifically limit the classes of monomers containing the carboxyl radical.
Particular preferred monomers containing phosphonate groups are vinylphosphonic acid and its salts.
Preferably the acetoacetate groups are provided by copolymerising addition polymerisable monomers containing acetoacetate functional groups.
Monomers containing other functional groups such as hydroxyl or carboxyl groups may be used.
Do not disclose the use of the acrylic monomers containing carbamate functionality for adhesive compositions.
The monomers containing carboxylic functionality are chosen from carboxylic acids containing ethylenic unsaturation.
These polymers include copolymers of styrene or substituted styrenes with vinyl monomers containing carboxyl groups.
Siloxane monomers containing an acroyl group are particularly effective in providing the desired oxygen permeability.
Synthetic polymers of monomers containing amide groups ; and.
Monomers containing other functional groups such as hydroxyl or amino groups may also be used.
Method for grafting hydrophilic monomers containing double bonds onto formed bodies with polymer surfaces.
Monomers containing acidic-groups can also be grafted onto polymers.
The preemulsion of the acrylic monomers containing the functional monomer AEHDB is thus obtained.
Nonionic copolymers of hydrophilic ( meth ) acrylates and of hydrophobic monomers containing a fatty chain.
Thereby the polymerizable monomers containing ligand can be oligomerized or polymerized to form a multivalent conjugate.
Copolymers of vinylpyrrolidone and of hydrophobic monomers containing a fatty chain ;.
Exemplary unsaturated monomers containing carboxylic acid groups are acrylic acid and methacrylic acid.
Non-crosslinked homopolymers and copolymers of monomers containing an amide group ;.
In some embodiments, no monomers containing dicyclopentadienyl groups are copolymerized.
In certain embodiments, suitable polymerizable monomers include monomers containing vinyl or acryl groups.
Of one or more monomers containing a carbon-carbon double bond.
Copolymers of vinylpyrrolidone and of hydrophobic monomers containing a fatty chain such as,.
Of two or more monomers containing a carbon-carbon double bond.
Preferred olefin monomers may also include aromatic-group-containing monomers containing up to 30 carbon atoms.
These monomers containing ethylenic unsaturation may be chosen in particular from,.
Copolymers of crotonic acid and of monomers containing at least one fatty chain ;.
The monomers containing amine or quaternary ammonium functions and corresponding to the formula,.
The olefinically unsaturated monomers are preferably monomers containing acrylate and / or methacrylate groups.
Diene monomers containing from 4 to 8 carbon atoms are generally preferred for commercial purposes.

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Examples of using Monomers
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