FATE OF POLYCYCLIC AROMATIC HYDROCARBONS DURING COMPOSTING OF OILY SLUDGE

2008 ◽  
Vol 29 (1) ◽  
pp. 43-53 ◽  
Author(s):  
M. Kriipsalu ◽  
M. Marques ◽  
W. Hogland ◽  
D. R. Nammari
2016 ◽  
Vol 35 (4) ◽  
pp. 437-444
Author(s):  
Shaoping Kuang ◽  
Wenjuan Yu ◽  
Yan Song ◽  
Yaqing Su ◽  
Huihui Wang ◽  
...  

2004 ◽  
Vol 70 (5) ◽  
pp. 3163-3166 ◽  
Author(s):  
Priyangshu Manab Sarma ◽  
Dhruva Bhattacharya ◽  
S. Krishnan ◽  
Banwari Lal

ABSTRACT A bacterial strain, PS4040, capable of degrading polycyclic aromatic hydrocarbons for use as the sole carbon source was isolated from oily-sludge-contaminated soil. The 16S rRNA gene showed 98.8% homology to that of Leclercia adecarboxylata. Comparative molecular typing with the clinical strain of L. adecarboxylata revealed that there were few comigrating and few distinct amplimers among them.


2019 ◽  
Vol 64 (1) ◽  
pp. 55-67
Author(s):  
Vlad Pӑnescu ◽  
◽  
Mihaela Cӑtӑlina Herghelegiu ◽  
Sorin Pop ◽  
Mircea Anton ◽  
...  

2019 ◽  
Author(s):  
Yachu Du ◽  
Kyle Plunkett

We show that polycyclic aromatic hydrocarbon (PAH) chromophores that are linked between two five-membered rings can access planarized structures with reduced optical gaps and redox potentials. Two aceanthrylene chromophores were connected into dimer model systems with the chromophores either projected outward (2,2’-biaceanthrylene) or inward (1,1’-biaceanthrylene) and the optical and electronic properties were compared. Only the planar 2,2’-biaceanthrylene system showed significant reductions of the optical gaps (1 eV) and redox potentials in relation to the aceanthrylene monomer.<br>


2019 ◽  
Author(s):  
Yachu Du ◽  
Kyle Plunkett

We show that polycyclic aromatic hydrocarbon (PAH) chromophores that are linked between two five-membered rings can access planarized structures with reduced optical gaps and redox potentials. Two aceanthrylene chromophores were connected into dimer model systems with the chromophores either projected outward (2,2’-biaceanthrylene) or inward (1,1’-biaceanthrylene) and the optical and electronic properties were compared. Only the planar 2,2’-biaceanthrylene system showed significant reductions of the optical gaps (1 eV) and redox potentials in relation to the aceanthrylene monomer.<br>


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