2023
DOI: 10.1039/d3re00354j
|View full text |Cite
|
Sign up to set email alerts
|

Operational parameters relevant to the examination of phosgene synthesis catalysis

Rory Hughes,
Giovanni E. Rossi,
David Lennon

Abstract: Large-scale phosgene synthesis, as encountered within isocyanate manufacturing chains, is typically performed by the reaction of carbon monoxide and dichlorine over an activated carbon catalyst. A modified micro-reactor arrangement is...

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 40 publications
0
1
0
Order By: Relevance
“…CO 2 is a renewable, nonflammable, nontoxic, and readily available C1 source. , Over the years, CO 2 has been captured and utilized in a variety of ways such as conventional capture, oxyfuel capture, precombustion capture, postcombustion capture, and cryogenic CO 2 capture. In addition, CO 2 was used in the CO 2 -philes, which were further used to develop surfactants and chelating agents. Furthermore, CO 2 is an efficient C1 feedstock in the synthesis of various chemicals such as formic acid, urea, methanol, cyclic carbonates, oxazolidine, urethanes, polycarbonates, benzimidazole, quinazoline, etc. Previously, phosgene methods were used for the synthesis of benzimidazole and quinazoline, but there were so many limitations that this method is now replaced by the catalytic process. The biggest hurdle for CO 2 fixation in value-added products is kinetic inertness and thermodynamic stability. Furthermore, kinetic inertness and catalytic pathways such as homogeneous, heterogeneous, photochemical, radiochemical, electrochemical, thermochemical, and biochemical pathways have been used. Thiols, halohydrocarbons, olefins, and amines are nucleophilic and N-heterocyclic compounds that are biocompatible and used in the medical industry. In addition, they are also used in plant growth regulators. Benzimidazole and quinazoline are important N-heterocyclic compounds that are widely used as the intermediate substrates for which C–N, C–S, C–C, and C–O bonds are formed via CO 2 .…”
Section: Introductionmentioning
confidence: 99%
“…CO 2 is a renewable, nonflammable, nontoxic, and readily available C1 source. , Over the years, CO 2 has been captured and utilized in a variety of ways such as conventional capture, oxyfuel capture, precombustion capture, postcombustion capture, and cryogenic CO 2 capture. In addition, CO 2 was used in the CO 2 -philes, which were further used to develop surfactants and chelating agents. Furthermore, CO 2 is an efficient C1 feedstock in the synthesis of various chemicals such as formic acid, urea, methanol, cyclic carbonates, oxazolidine, urethanes, polycarbonates, benzimidazole, quinazoline, etc. Previously, phosgene methods were used for the synthesis of benzimidazole and quinazoline, but there were so many limitations that this method is now replaced by the catalytic process. The biggest hurdle for CO 2 fixation in value-added products is kinetic inertness and thermodynamic stability. Furthermore, kinetic inertness and catalytic pathways such as homogeneous, heterogeneous, photochemical, radiochemical, electrochemical, thermochemical, and biochemical pathways have been used. Thiols, halohydrocarbons, olefins, and amines are nucleophilic and N-heterocyclic compounds that are biocompatible and used in the medical industry. In addition, they are also used in plant growth regulators. Benzimidazole and quinazoline are important N-heterocyclic compounds that are widely used as the intermediate substrates for which C–N, C–S, C–C, and C–O bonds are formed via CO 2 .…”
Section: Introductionmentioning
confidence: 99%