Eutrophication-induced regime shifts reduced sediment burial ability for polycyclic aromatic hydrocarbons: Evidence from Lake Taihu in China

Chemosphere ◽  
2021 ◽  
Vol 271 ◽  
pp. 129709
Author(s):  
Yuqiang Tao
2011 ◽  
Vol 184 (11) ◽  
pp. 6815-6825 ◽  
Author(s):  
Guanghui Guo ◽  
Fengchang Wu ◽  
Hongping He ◽  
Ruiqing Zhang ◽  
Chenglian Feng ◽  
...  

2015 ◽  
Vol 17 (6) ◽  
pp. 1150-1156 ◽  
Author(s):  
Zhonghua Zhao ◽  
Lu Zhang ◽  
Jianming Deng ◽  
Jinglu Wu

Seasonal distribution of organochlorine pesticides (OCPs) and polycyclic aromatic hydrocarbons (PAHs) and their possible interactions with phytoplankton species in water from Lake Taihu were investigated.


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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