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Rahmatollah Rahimi

Researcher at Iran University of Science and Technology

Publications -  173
Citations -  2846

Rahmatollah Rahimi is an academic researcher from Iran University of Science and Technology. The author has contributed to research in topics: Photocatalysis & Porphyrin. The author has an hindex of 26, co-authored 158 publications receiving 2139 citations. Previous affiliations of Rahmatollah Rahimi include University of Washington.

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Investigation of the catalytic activity of nano-sized CuO, Co3O4 and CuCo2O4 powders on thermal decomposition of ammonium perchlorate

TL;DR: In this article, nano-sized CuO, Co 3 O 4 and CuCo 2 O 4 powders were prepared via different methods such as co-precipitation, thermal decomposition of oxalate precursor and sol-gel and their catalytic activities towards thermal deformation of ammonium perchlorate.
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Synthesis, characterization and adsorbing properties of hollow Zn-Fe2O4 nanospheres on removal of Congo red from aqueous solution

TL;DR: In this paper, a facile solvothermal method using ultrasonic waves was used to synthesize hollow zinc ferrite nanosphere for removal of Congo Red (CR) in the wastewater treatment.
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Visible light photocatalytic disinfection of E. coli with TiO 2 -graphene nanocomposite sensitized with tetrakis(4-carboxyphenyl)porphyrin

TL;DR: In this article, the authors developed a new heterogeneous photocatalysis system for disinfection of bacteria from wastewater by using TiO2-graphene (TG) nanocomposite sensitized with tetrakis(4-carboxyphenyl)porphyrin (TCPP).
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Efficient oxidation and epoxidation using a chromium(VI)-based magnetic nanocomposite

TL;DR: In this paper, a hybrid chromium-VI-based magnetic nanocomposite catalyst by co-precipitation was used for the oxidation of alcohols and alkenes to aldehydes, ketones and epoxides.
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Steric and inductive effects on the basicity of porphyrins and on the site of protonation of porphyrin dianions: radiolytic reduction of porphyrins and metalloporphyrins to chlorins or phlorins

TL;DR: A series of sulfonated, water-soluble, phenyl-substituted porphyrins has been prepared, containing halogen or alkyl groups in the ortho, di-ortho or para positions as discussed by the authors.