Examples of 'internal olefins' in a sentence
Meaning of "internal olefins"
internal olefins: Unsaturated hydrocarbons that contain a double bond within the carbon chain structure, often used in chemical reactions and industrial processes
How to use "internal olefins" in a sentence
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internal olefins
The process applies in particular to internal olefins.
A mixture of internal olefins may be used.
Process for the oligomerization of internal olefins.
Internal olefins can be reacted with ethene to produce smaller olefins.
A further hydrophobe source is from internal olefins.
The amount of branched internal olefins in the feed stream is not limited.
The major impurity was vinylidene olefinic isomer and some internal olefins.
The sulphonation of the internal olefins is preferably carried out with sulphur trioxide.
These olefins may be branched or linear olefins and either terminal or internal olefins.
Process for the isomerization of external olefins to internal olefins concomitantly with diolefin hydrogenation.
Internal olefins and terminal olefins are suitable as well as linear and branched olefins.
The present invention relates to a process for separating functionalized alpha olefins from functionalized internal olefins.
A process for sulfonating internal olefins comprising,.
These catalyst systems facilitate isomerization of a-olefins to internal olefins.
In many industrial streams, internal olefins frequently are also found as well as terminal alkenes.
See also
These olefins are alpha-olefins that have been converted to internal olefins.
These internal olefins may be linear or branched, but are preferably linear or lightly branched.
Isomerized alpha-olefins are alpha-olefins that have been converted to internal olefins.
The odd carbon internal olefins were a result of double bond migration, followed by cross metathesis.
The non-aqueous fluids used in brazil are based on n-paraffin and internal olefins.
Representative example for the synthesis of internal olefins from the self-metathesis of alpha olefins.
The present invention relates to a process for producing sulfonated detergent-range internal olefins.
Synthesis of methyl substituted internal olefins from the self-metathesis of methyl substituted alpha olefins.
Although mainly alpha-olefins are produced, some vinylidene and internal olefins also result.
Less than 4.3 % internal olefins resulting from isomerization were present.
In another embodiment, the host cell has OleBCD activity for the production of internal olefins.
Similarly, the trimer fraction predominantly contained four internal olefins having a single branched alkyl chain.
The prior art phosphite ( Ligand C ) shows much lower activity when starting from internal olefins.
Preferred are internal olefins having from 4 to 24 carbon atoms, or mixtures thereof.
The alpha-olefins are readily separated from the corresponding branched and internal olefins by this method.
The di-substituted internal olefins include beta internal olefins having the chemical formula R-CH=CH-CH3.
For ASA-production a-olefins need to be isomerized to form internal olefins.
The olefin may also include C4-C9 internal olefins.
More preferably, at least 75 wt % of the olefin feed is comprised of internal olefins.
Preferred olefins also include C4-C9 internal olefins.
Useful olefinic compounds may be terminal olefins, i.e., olefins having a group, or internal olefins.
A further hydrophobe source for formula ( II ) is from internal olefins.
In fact, the feed stream may contain as little as 1 wt. % of internal olefins.
The distillate cuts were predominantly C6-9-carbon chain internal olefins.
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