Zhakiyeva, Zhanar
 
(2017)
Characterisation and speciation of particulate matter deposited on PTFE and quartz filters.
[Laurea magistrale], Università di Bologna, Corso di Studio in 
Chimica industriale [LM-DM270]
   
  
  
        
        
	
  
  
  
  
  
  
  
    
  
    
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      Abstract
      Respirable fractions of airborne ambient particulate matter have been identified over the years as potential health hazards. Due to chemical complexity, extremely small particle sizes, small sample size collected on filters, analysis of such samples is quite problematic. The technique that has a great potential for elemental speciation of fine PM inside the bulk of the filter is a synchrotron-based XAFS spectroscopy. This technique allows to identify the form of an occurrence of an element in the complex mixture, complementing compositional elemental data obtained by X-ray fluorescence and PIXE. Additionally, XAFS is non-destructive and sensitive to ppm concentration levels of many elements when the signals are detected in fluorescence mode. However, it is well known that chemical composition of airborne PM on the surface differs from that of the core. Moreover, many studies have shown that there is a good correlation between the surface composition of aerosol particles and their role in environmental processes, such as atmospheric scavenging and cloud condensation nuclei. Therefore, an XPS was employed to investigate the surface composition of PM. XPS is a non-destructive technique that requires minimum sample preparation. Furthermore, XANES K-edge spectra simulations using FDMNES code were performed in order to simulate lacking reference data. We went even further and performed FDMNES calculations for intermediate energy of sulphur K-edge. Previously such XAS simulations were done in solitary cases, therefore our interest was justified. Following the pre-edge and XANES analyses outcomes of the three investigated filters, and by considering the relative abundance of the metals in them, an EXAFS analysis at the Fe K-edge only was performed. It provided quantitative data of the selected metal core bonding, was performed. In particular the local atomic environment of the Fe site has been revealed, providing bond length referring mostly to the first coordination shell.
     
    
      Abstract
      Respirable fractions of airborne ambient particulate matter have been identified over the years as potential health hazards. Due to chemical complexity, extremely small particle sizes, small sample size collected on filters, analysis of such samples is quite problematic. The technique that has a great potential for elemental speciation of fine PM inside the bulk of the filter is a synchrotron-based XAFS spectroscopy. This technique allows to identify the form of an occurrence of an element in the complex mixture, complementing compositional elemental data obtained by X-ray fluorescence and PIXE. Additionally, XAFS is non-destructive and sensitive to ppm concentration levels of many elements when the signals are detected in fluorescence mode. However, it is well known that chemical composition of airborne PM on the surface differs from that of the core. Moreover, many studies have shown that there is a good correlation between the surface composition of aerosol particles and their role in environmental processes, such as atmospheric scavenging and cloud condensation nuclei. Therefore, an XPS was employed to investigate the surface composition of PM. XPS is a non-destructive technique that requires minimum sample preparation. Furthermore, XANES K-edge spectra simulations using FDMNES code were performed in order to simulate lacking reference data. We went even further and performed FDMNES calculations for intermediate energy of sulphur K-edge. Previously such XAS simulations were done in solitary cases, therefore our interest was justified. Following the pre-edge and XANES analyses outcomes of the three investigated filters, and by considering the relative abundance of the metals in them, an EXAFS analysis at the Fe K-edge only was performed. It provided quantitative data of the selected metal core bonding, was performed. In particular the local atomic environment of the Fe site has been revealed, providing bond length referring mostly to the first coordination shell.
     
  
  
    
    
      Tipologia del documento
      Tesi di laurea
(Laurea magistrale)
      
      
      
      
        
      
        
          Autore della tesi
          Zhakiyeva, Zhanar
          
        
      
        
          Relatore della tesi
          
          
        
      
        
          Correlatore della tesi
          
          
        
      
        
          Scuola
          
          
        
      
        
          Corso di studio
          
          
        
      
        
          Indirizzo
          Advanced Spectroscopy in Chemistry
          
        
      
        
      
        
          Ordinamento Cds
          DM270
          
        
      
        
          Parole chiave
          XAFS XPS FDMNES particulate matter
          
        
      
        
          Data di discussione della Tesi
          19 Luglio 2017
          
        
      
      URI
      
      
     
   
  
    Altri metadati
    
      Tipologia del documento
      Tesi di laurea
(NON SPECIFICATO)
      
      
      
      
        
      
        
          Autore della tesi
          Zhakiyeva, Zhanar
          
        
      
        
          Relatore della tesi
          
          
        
      
        
          Correlatore della tesi
          
          
        
      
        
          Scuola
          
          
        
      
        
          Corso di studio
          
          
        
      
        
          Indirizzo
          Advanced Spectroscopy in Chemistry
          
        
      
        
      
        
          Ordinamento Cds
          DM270
          
        
      
        
          Parole chiave
          XAFS XPS FDMNES particulate matter
          
        
      
        
          Data di discussione della Tesi
          19 Luglio 2017
          
        
      
      URI
      
      
     
   
  
  
  
  
  
    
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