z-logo
open-access-imgOpen Access
SrCrxFe12-xO19 nanoceramics as an effective catalyst for desulfurization of liquid fuels: Green sol-gel synthesis, characterization, magnetic and optical properties
Author(s) -
Samira Mandizadeh,
Faezeh Soofivand,
Samira Bagheri,
Masoud SalavatiNiasari
Publication year - 2017
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0162891
Subject(s) - flue gas desulfurization , nanoparticle , catalysis , materials science , adsorption , chemical engineering , combustion , sulfur , coercivity , nuclear chemistry , nanotechnology , chemistry , organic chemistry , metallurgy , engineering , physics , condensed matter physics
In this work, SrCr x Fe 12-x O 19 (x = 0.0, 0.5, 1.0, 1.5) nanostructures were successfully synthesized by sol-gel auto-combustion method, and different aminoacids were used as green reductants. Various analysis results show that SrCr x Fe 12-x O 19 nanoparticles synthesized successfully.The present study shows that SrCr x Fe 12-x O 19 nanoparticle could be used as adsorbent for the desulfurization of liquid fuels. Increasing of nanoparticles concentration was caused to increase the adsorption rate of sulfur contents of fuel. The adsorption rate of sulfur contents of fuel in various concentrations 4.5, 9.5, and 18.5 g. L -1 of SrCr x Fe 12-x O 19 nanoparticles in solution was estimated about 39, 50, and 62% for 30 min, respectively. The results of catalytic tests reveals that SrCr x Fe 12-x O 19 nanoparticles have the potential to be used as a new kind of semiconductor catalysts for the desulfurization of liquid fuels. Magnetic property of the final sample was measured at room temperature by a vibration sample magnetometer (VSM) and shown that the intrinsic coercivity of product is about 6000 Oe and it exhibits characteristics of single magnetic domains (M r / M s = 0.53).

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here