Polycyclic aromatic hydrocarbons in milk and dairy products

2018 ◽  
Vol 72 (1) ◽  
pp. 120-131 ◽  
Author(s):  
Shabboo Amirdivani ◽  
Nasim Khorshidian ◽  
Maryam Ghobadi Dana ◽  
Reza Mohammadi ◽  
Amir M Mortazavian ◽  
...  
1968 ◽  
Vol 51 (1) ◽  
pp. 122-129 ◽  
Author(s):  
John W Howard ◽  
Thomas Fazio ◽  
Richard H White ◽  
Barbara A Klimeck

Abstract A general method for polycyclic aromatic hydrocarbons and a specific procedure for benzo(a)pyrene in various total diet composites (dairy products; oils, fats, and shortenings; beverages; meat, fish, and poultry; and root vegetables) have been developed. Recoveries ranged from 75 to 100% at the 2 ppb level. Pyrene and fluoranthene were found to be present in all of the total diet samples analyzed. Trace quantities of benzo ( a ) pyrene, benzo(k)- fluoranthene, benzo ( b ) fluoranthene, and other hydrocarbons were isolated from various lots of the oils, fats, and shortenings composites.


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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