Mametja, MB2010-09-292010-09-292008-11Mametja, MB. 2008. An investigation of the molecular properties of 1,1,1-trichloroethane using laser spectroscopy. Dissertation submitted in partial fulfilment of the requirements for the degree Master of Science at the Potchefstroom campus of the North-West Universityhttp://hdl.handle.net/10204/4407Copyright: 2008 North-West University. Dissertation submitted in partial fulfilment of the requirements for the degree Master of Science at the Potchefstroom campus of the North-West UniversityFT-IR and FT-Raman spectra of 1,1,1-trichlorethane (CH3CCl3) were recorded in the regions 400 – 3500 cm-1 and 200 – 3500 cm-1 respectively. The observed vibrational numbers were analysed and assigned to different normal modes of vibration of the molecule. Density functional calculations were performed to support wavenumber assignment of the observed bands. The equilibrium geometry and harmonic wavenumbers of TCE were calculated with the DFT B3LYP method [Spartan, 2004]. The vibrational wavenumbers were compared with IR experimental data. The discrepancies between the calculated and observed spectra is that the rotational energy levels cause splitting or broadening of infrared absorbance peaks and this refinement was not included in the calculations using Spartan [2004]. Ultravioletvisible absorption spectroscopy was used to determine the wavelength needed for excitation and ionization of TCE and it was confirmed that the absorption of energy by TCE is in the deep UV region. The time of flight mass spectra of ion products formed from TCE were recorded after excitation by nanosecond and femtosecond laser pulses at various wavelengths and at various different conditions. The mass spectra obtained at different conditions with both lasers were compared in order to find information about ionization and dissociation of the molecule. The parent ion was not detected in either nanosecond or femtosecond experiments, probably due to the molecule being dissociated easily. The main difference between nanosecond and femtosecond laser pulse ionization of TCE is that more larger fragments are observed when using femtosecond laser pulses, due to ladder climbing being dominant, while ladder switching is dominant in the nanosecond regime.enTrichloroethaneLaser spectroscopyVibrational wavenumbersNorth-West UniversityReportMametja, M. (2008). <i>An investigation of the molecular properties of 1,1,1-trichloroethane using laser spectroscopy</i> (Student Number). North-West University. Retrieved from http://hdl.handle.net/10204/4407Mametja, MB <i>An investigation of the molecular properties of 1,1,1-trichloroethane using laser spectroscopy.</i> Student Number. North-West University, 2008. http://hdl.handle.net/10204/4407Mametja M. An investigation of the molecular properties of 1,1,1-trichloroethane using laser spectroscopy. 2008 [cited yyyy month dd]. Available from: http://hdl.handle.net/10204/4407TY - Report AU - Mametja, MB AB - FT-IR and FT-Raman spectra of 1,1,1-trichlorethane (CH3CCl3) were recorded in the regions 400 – 3500 cm-1 and 200 – 3500 cm-1 respectively. The observed vibrational numbers were analysed and assigned to different normal modes of vibration of the molecule. Density functional calculations were performed to support wavenumber assignment of the observed bands. The equilibrium geometry and harmonic wavenumbers of TCE were calculated with the DFT B3LYP method [Spartan, 2004]. The vibrational wavenumbers were compared with IR experimental data. The discrepancies between the calculated and observed spectra is that the rotational energy levels cause splitting or broadening of infrared absorbance peaks and this refinement was not included in the calculations using Spartan [2004]. Ultravioletvisible absorption spectroscopy was used to determine the wavelength needed for excitation and ionization of TCE and it was confirmed that the absorption of energy by TCE is in the deep UV region. The time of flight mass spectra of ion products formed from TCE were recorded after excitation by nanosecond and femtosecond laser pulses at various wavelengths and at various different conditions. The mass spectra obtained at different conditions with both lasers were compared in order to find information about ionization and dissociation of the molecule. The parent ion was not detected in either nanosecond or femtosecond experiments, probably due to the molecule being dissociated easily. The main difference between nanosecond and femtosecond laser pulse ionization of TCE is that more larger fragments are observed when using femtosecond laser pulses, due to ladder climbing being dominant, while ladder switching is dominant in the nanosecond regime. DA - 2008-11 DB - ResearchSpace DP - CSIR KW - Trichloroethane KW - Laser spectroscopy KW - Vibrational wavenumbers KW - North-West University LK - https://researchspace.csir.co.za PY - 2008 T1 - An investigation of the molecular properties of 1,1,1-trichloroethane using laser spectroscopy TI - An investigation of the molecular properties of 1,1,1-trichloroethane using laser spectroscopy UR - http://hdl.handle.net/10204/4407 ER -