Emissions of polycyclic aromatic hydrocarbons from fluidized and fixed bed incinerators disposing petrochemical industrial biological sludge

2009 ◽  
Vol 168 (1) ◽  
pp. 438-444 ◽  
Author(s):  
Lin-Chi Wang ◽  
Long-Full Lin ◽  
Soon-Onn Lai
2020 ◽  
Vol 71 (6) ◽  
pp. 346-354
Author(s):  
Ioana Alexandra Ionescu ◽  
Viorel Patroescu ◽  
Mihai Stefanescu ◽  
Vasile Iancu ◽  
Florentina Laura Chiriac ◽  
...  

This paper shows the influence of certain biological sludge disintegration processes over the concentrations of emerging pollutants, including classes of structurally different compounds such as pharmaceuticals, hormones and polycyclic aromatic hydrocarbons from anaerobic stabilized sludge. Three processes for sludge disintegration were tested: ultrasonic, ultrasonic + electrokinetic and ultrasonic + electrokinetic + microbubble generation. Activated sludge from an urban wastewater treatment plant was used in the experiments. Both pharmaceuticals from the analgesic and antipyretic classes, as well as the identified hormones (estrone) and polycyclic aromatic hydrocarbons (PAHs), were sensitive to the disintegration processes applied, the experimental results showing the decrease of their concentration correlated with the increase of the disintegration energy.


Author(s):  
M. Tian ◽  
B. S. Liu ◽  
M. Hammonds ◽  
N. Wang ◽  
P. J. Sarre ◽  
...  

Polycyclic aromatic hydrocarbons (PAHs) are known to be present in many astrophysical objects and environments, but our understanding of their formation mechanism(s) is far from satisfactory. In this paper, we describe an investigation of the catalytic conversion reaction of acetylene gas to PAHs over pyroxene and alumina. Crystalline silicates such as pyroxenes (with general formula [Mg, Fe]SiO 3 ) and alumina (Al 2 O 3 ) are observed astrophysically through their infrared spectra and are likely to promote grain surface chemical reactions. In the experiments reported here, gas-phase PAHs were produced by the catalytic reaction of acetylene over crystalline silicates and alumina using a pulsed jet expansion technique and the gaseous products detected using time-of-flight mass spectrometry. In a separate experiment, the catalytic formation of PAHs from acetylene was further confirmed with acetylene gas at atmospheric pressure flowing continuously through a fixed-bed reactor. The gas effluent and carbonaceous compounds deposited on the catalysts were dissolved separately in dichloromethane and analysed using gas chromatography–mass spectrometry. Among the samples studied, alumina showed higher activity than the pyroxene-type grains for the acetylene reaction. It is proposed that formation of the PAHs relies on the Mg 2+ ions in the pyroxenes and Al 3+ ions in alumina, where these ions act as Lewis acid sites. X-ray diffraction, Fourier transform infrared and high-resolution transmission electron microscopy techniques were used to characterize the structure and physical properties of the pyroxene and alumina samples.


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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