Examples of 'aliphatic diols' in a sentence
Meaning of "aliphatic diols"
aliphatic diols: organic compounds with two hydroxyl groups attached to aliphatic carbon chains
How to use "aliphatic diols" in a sentence
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aliphatic diols
Aliphatic diols are preferred in one embodiment.
Examples of further aliphatic diols are linear or branched diols.
Aliphatic diols and glycol ether solvents are most preferred solvents.
A mixture of cycloaliphatic and aliphatic diols can also be used.
These aliphatic diols may be used individually or in combination.
Suitable polyols include long chain aliphatic diols and polyoxyalkylene ethers.
Aliphatic diols and triols are believed to impart flexibility to the final copolymer.
The preferred polyols are aliphatic diols and especially polypropylene glycol.
The polymer is obtained by copolymerization with a monomer chosen from aliphatic diols and oligomeric ethers.
Advantageously, the aliphatic diols are linear saturated diols.
Suitable alcohols, reactable with carboxylic acids to obtain a polyester include aliphatic diols.
The aliphatic diols and diacids may be linear, branched or cyclic.
Representative of the preferred chain extenders are aliphatic diols and aromatic diamines.
Aliphatic diols are used as the alcohol component of the biomass-derived polymerization raw material.
Process for the co-production of aliphatic diols and cyclic ethers.
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Typical saturated aliphatic diols preferably include the lower alkane-diols such as ethylene glycol.
Further, the alcohol components may include cycloaliphatic diols and aliphatic diols.
Aliphatic diols having from about 2 to about 12 carbon atoms are preferred.
Preferred first alcohols include aliphatic diols having an aliphatic side-chain substituent.
The biodegradable aliphatic polyesters from diacid-diol comprise aliphatic diacids and aliphatic diols.
Especially preferred are aliphatic diols containing 2-8 carbon atoms.
Useful alcohols, reactable with the carboxylic acids to obtain the polyester include aliphatic diols.
Particular preference is given to aliphatic diols having 2-8 carbon atoms.
The first alcohol can be selected from aliphatic and aromatic diols, preferably aliphatic diols.
Particularly preferred are aliphatic diols containing from 2 to 8 carbon atoms.
The crystallinity and melting point characteristics are modified utilizing alkanolamines, aliphatic diols and cycloaliphatic diols.
Especially preferred aliphatic diols are those that have 2 to 6 carbon atoms.
In another embodiment, the compounds ( 4 ) are aliphatic diols.
In addition, aliphatic diols or triols with 2 to 6 carbon atoms are also preferred.
The preferred compounds ( 4 ) are aliphatic diols.
The aliphatic diols for producing the prepolymers of ( 2 ) and ( 4 ) are not particularly limited.
Particularly preferred are aliphatic diols having 2-54 carbon atoms.
In at least one embodiment, the compounds ( 4 ) are aliphatic diols.
The diols include branched, unbranched, and cyclic aliphatic diols having from 2 to 12 carbon atoms.
Ethylene glycol and 1,4-butanediol are the preferred aliphatic diols.
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Such chiral diols are important in organic synthesis
Preparation of perfluoropolyether diols with high functionality
Saturated diols can be produced by different methods
Examples of using Aliphatic
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Halogenated derivatives of the aliphatic or alicyclic hydrocarbons
Various aliphatic and aromatic hydrocarbon peaks
It consists predominantly of aliphatic hydrocarbons having and
