Examples of 'carbonylation reaction' in a sentence
Meaning of "carbonylation reaction"
carbonylation reaction - A chemical reaction in which a carbonyl group is introduced into a compound
How to use "carbonylation reaction" in a sentence
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carbonylation reaction
The results of the carbonylation reaction were identical.
A mechanism is proposed for the reductive carbonylation reaction.
The carbonylation reaction requires the presence of a catalytic system.
It is also possible to perform this carbonylation reaction electrochemically.
The carbonylation reaction is conveniently carried out at moderate temperatures.
This catalyst was used directly in the above carbonylation reaction.
The liquid carbonylation reaction composition may comprise water.
These volatile components may be recycled to the carbonylation reaction.
The carbonylation reaction is carried out in the vapor phase.
Any catalyst system effective in the carbonylation reaction may be employed.
The exothermic carbonylation reaction of the present invention is preferably catalysed.
These other compounds may be recycled to the carbonylation reaction zone.
The carbonylation reaction is preferably carried out continuously in a gas phase.
Hydrogen may be added to the carbonylation reaction to improve reaction rate.
The carbonylation reaction produces hydrogen by a reaction of carbon monoxide with water.
See also
A water balance then remains within the carbonylation reaction system.
The carbonylation reaction of the invention is also carried out in the presence of water.
A particularly preferred carboxylic acid is the acid product of the carbonylation reaction.
The primary reaction product of the carbonylation reaction may also be used as a solvent.
A number of catalyst systems are at present known which promote the carbonylation reaction.
The quantity of acid used in the carbonylation reaction may vary within ranges.
The presence of small amounts of hydrogen is generally not detrimental to the carbonylation reaction.
The carbonylation reaction according to the invention is carried out at moderate temperatures and pressures.
The carboxylic acid may serve as the solvent of the carbonylation reaction.
The carbonylation reaction system may further include hydrogen in the carbon monoxide feed.
The reaction conditions for the above carbonylation reaction can vary to a certain extent.
The carbonylation reaction proceeds as methanol and carbon monoxide are continuously fed to the reactor.
A variant consists in adding these group VIb corrosion metals to the carbonylation reaction medium.
Catalysts usually employed in the carbonylation reaction comprise a rhodium compound promoted with methyl iodide.
The inventive process solves a problem associated with low water carbonylation reaction systems.
The carbonylation reaction for Example XIII was carried out as follows.
Halide containing liquids include liquid or vaporous organic materials such as carbonylation reaction products.
The carbonylation reaction is carried out as follows,.
Recycling the said homogeneous liquid obtained into the medium subjected to the carbonylation reaction.
In general, the carbonylation reaction requires a rather complex catalyst.
The iodides may also originate from corrosive metals appearing during the carbonylation reaction.
Finally, the carbonylation reaction is carried out in the presence of a solvent.
The low water conditions makes it difficult to remove corrosion metals from the carbonylation reaction.
A carbonylation reaction was carried out using the following amounts of reactants,.
Another disadvantage of this process is that the multidentate phosphines decompose during the carbonylation reaction.
A carbonylation reaction was carried out on a pressure flow reactor unit comprising 16 reactors.
Multidentate phosphine ligands may, if desired, be present during the carbonylation reaction.
More preferably, the carbonylation reaction is conducted under low water conditions.
Furthermore, the reaction pressure is too low to conduct an efficient carbonylation reaction.
A separate carbonylation reaction using phosgene, ethyl chloroformate or some similar reagent is avoided.
However, the use of zeolites to catalyse the carbonylation reaction is not exemplified.
The carbonylation reaction described in Example 1 was carried out in the presence of,.
In step ( a ) of the process of the invention the actual carbonylation reaction takes place.
Conveniently, however, the carbonylation reaction may be carried out in the additional presence of a solvent.
More particularly, it relates to the improvement of diaryl carbonate yield in the carbonylation reaction.
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