(13.58.121.214)
Users online: 12807     
Ijournet
Email id
 

Research Journal of Engineering and Technology
Year : 2010, Volume : 1, Issue : 1
First page : ( 24) Last page : ( 26)
Print ISSN : 0976-2973.

Synthesis and characterization of some Cobalt Phthalocyanine Carboxylamide used in the Merox Process

Choudhary Rumi1,*, Chaudhari PK1, Keshav Amit1, Singh RK2

1Department of Chemical Engineering, National Institute of Technology (NIT), Raipur

2Indian Institute of Petroleum, Dehradun

*Corresponding Author E-mail: rumi.chem@gmail.com, rumi28@rediffmail.com

Online published on 7 March, 2013.

Abstract

Phthalocyanines (Pc) are widely used as catalysts in the process of removal of mercaptans in petroleum refining industries. Conventional separation processes using organic solvents could not be used in the above process as many Pc compounds have intermolecular interactions with macrocycles and the complexes are practically insoluble in these solvents. Considerable efforts have been made to generate new Pc derivatives possessing enhanced solubility characteristics. It has been found that Pc compounds bearing liophilic/hydrophilic substituents on the periphery such as different metals modulate the catalytic activity to a great extent. In the present paper, new Pc catalysts were synthesized [cobalt phthalocyanine tetra-carboxylamide (CoPc(CONH2)4) and cobalt phthalocyanine di-carboxylamide (CoPc(CONH2)2] using facile synthetic route and characterized by C,H,N,MS,UV-Vis and IR. The activity of the generated catalysts could be further compared with the simple un-substituted metal phthalocyanine and some commercial catalysts.

Top

Keywords

Phthalocyanines, catalyst, catalytic activity, solubility, derivatives.

Top

 
║ Site map ║ Privacy Policy ║ Copyright ║ Terms & Conditions ║ Page Rank Tool
747,498,423 visitor(s) since 30th May, 2005.
All rights reserved. Site designed and maintained by DIVA ENTERPRISES PVT. LTD..
Note: Please use Internet Explorer (6.0 or above). Some functionalities may not work in other browsers.