Examples of 'olefins can' in a sentence
Meaning of "olefins can"
olefins can: Likely incomplete phrase, but 'olefins' refer to a group of unsaturated hydrocarbons
How to use "olefins can" in a sentence
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olefins can
The olefins can be linear or branched olefins.
Mixtures of two or more olefins can also be polymerized.
The olefins can be aliphatic or alicyclic.
A good overview of the general state of hydroformylation of olefins can be found in.
These alpha olefins can be linear or branched.
After 1 hour no acetylenes and no olefins can be found.
Olefins can be produced by dehydration of the corresponding alcohol.
Mixtures of olefins can be used.
Olefins can also be produced in fluid catalytic cracking process units.
One or two or more olefins can be used for the polymerization.
Olefins can be unstable compounds that result in the formation of tars in petroleum products.
A wide range of fluorinated olefins can be used in the practice of this invention.
The olefins can be used together in the process, giving modified homopolymers or copolymers.
It is known that one or more olefins can be polymerized in a gaseous phase reaction.
For example, homopolymerization of propene or copolymerization between propene and other olefins can be adopted.
See also
A wide range of olefins can be used for the prepolymerization.
After 2 hours no acetylenes and no olefins can be found.
One way in which olefins can be made is by catalytic conversion.
Of course, also mixture constituted by a plurality of olefins can be hydroformylated as well.
A wide range of olefins can be used for the polymerization.
After 30 min no acetylenes and no olefins can be found.
Suitable olefins can in general be obtained from any source.
By the aldehyde addition of phosphoryl group-substituting carbanions, olefins can be obtained through a Wittig-like mechanism.
Other alpha olefins can be polymerized with the ethylene also.
After 35 min no acetylenes and traces of olefins can be found.
Higher olefins can be used but have no additional advantages per se.
The second key point is that alpha olefins can be a major product of F-T chemistry.
Said olefins can come from non-fossil resources such as biomass.
As well as the conjugated diene, smaller quantities of C2-C5 olefins can also be present.
Internal olefins can be reacted with ethene to produce smaller olefins.
Any of the isomeric olefins can be used, alone or as mixtures.
Use of cyclic olefins can result in the formation ofpolymers having narrow molecular weight distributions.
The above-mentioned other olefins can be employed singly or in combination.
The olefins can undergo allylic oxidation with chromium or preferably selenium reagents see Rabjohn, Org.
In this oxygenate conversion process, olefins can generally be produced at a wide range of temperatures.
The olefins can for this reason be classified into two distinct categories,.
Very pure non-branched linear alpha olefins can be obtained by multiple passes through the process.
The olefins can also be cyclic in structure, the ring comprising 3 to 20 carbon atoms.
Geometric isomers of olefins can also be present in the compounds described herein.
These branched olefins can be converted into branched alcohols and subsequently into surfactant sulphates.
In some cases blends of olefins can be used to prepare mixed dialkyl magnesium.
These olefins can be aliphatic, aromatic, cyclic or other olefins.
More generally, the olefins can be linear branched or cyclic.
The unreacted olefins can be separated by means of the conventional methods, and recycled.
The resulting olefins can then be hydroborated e . g.
Before the raw olefins can be used, they usually must be separated from these mixtures.
Dienes and cyclic olefins can also be homo - or copolymerized.
In general, those olefins can be classified for that reason into two distinct categories,.
Generally, the blend of alpha olefins can be a blend of any alpha olefin described herein.
For this reason, olefins can be classified into two separate categories,.
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