Current-density maps as probes of aromaticity: Global and Clar π ring currents in totally resonant polycyclic aromatic hydrocarbons

2007 ◽  
Vol 135 ◽  
pp. 309-323 ◽  
Author(s):  
Erich Steiner ◽  
Patrick W. Fowler ◽  
Alessandro Soncini ◽  
Leonardus W. Jenneskens
2008 ◽  
Vol 14 (10) ◽  
pp. 3093-3099 ◽  
Author(s):  
Stijn Fias ◽  
Patrick W. Fowler ◽  
Juan Luis Delgado ◽  
Uwe Hahn ◽  
Patrick Bultinck

2003 ◽  
Vol 9 (13) ◽  
pp. 2974-2981 ◽  
Author(s):  
Alessandro Soncini ◽  
Erich Steiner ◽  
Patrick W. Fowler ◽  
Remco W. A. Havenith ◽  
Leonardus W. Jenneskens

2017 ◽  
Vol 24 (3) ◽  
pp. 397-404 ◽  
Author(s):  
Asim Yaqub ◽  
Mohamed Hasnain Isa ◽  
Huma Ajab ◽  
Shamsul Rahman Kutty ◽  
Ezerie H. Ezechi

Abstract Produced water is actually the wastewater separated from petroleum crude oil. Electrochemical-oxidation experiments was conducted for degradation of 16 priority polycyclic aromatic hydrocarbons (PAHs) using DSA type Ti/IrO2 anode. Laboratory scale batch reactor was used for degradation studies. To get the maximum PAHs removal electrochemical process optimized on three independent variable current density, pH and electrolysis time. The response surface modelling (RSM) based on a Box-Behnken design was applied to get appropriate experimental design. X1, X2 and X3 are the coded factors of independent variables such as the current density, pH and electrolysis time, respectively. Maximum removal was 95.29% at optimized conditions such as current density of 9 mA/cm2, pH 3 and electrolysis time 3.7 h. Quadratic model was suggested best fit model. The results of the Analysis of Variances (ANOVA) for PAHs demonstrated that the model was highly significant.


2019 ◽  
Vol 21 (22) ◽  
pp. 11564-11568 ◽  
Author(s):  
Guglielmo Monaco ◽  
Riccardo Zanasi

The anisotropy of the magnetically induced current density tensor can be computed by its original formulation, known in the literature as ACID, or by its revised definition, AACID, which takes into account the asymmetric nature of the tensor. In polycyclic aromatic hydrocarbons, the excess of the integrated value of AACID over that computed for isolated ethylenes correlate with the Hückel delocalization energy.


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