The photodissociation of 1-bromobutane is explored using pump-probe spectroscopy and time-of-flight mass spectrometry. Fragments of bromobutane are constructed computationally and theoretical energies are calculated using Gaussian 16 software. It is determined that the dissociation of bromine from the parent molecule is the most observed fragmentation pathway arising from the excitation of the ground state parent molecule to a dissociative A state using two 400 nm, 3.1 eV pump photons. The dissociation energy of this pathway is 2.91 eV, leaving 3.3 eV of energy that is redistributed into the product fragments as vibrational energy. C4H9 has the highest relative intensity in the mass spectrum with a relative intensity of 1.00. It is followed by C2H5 and C2H4 at relative intensities of 0.73 and 0.29 respectively. Because of the negative correlation between C4H9 and these two fragments at positive time delays, it is concluded that most of these smaller molecules are formed from the further dissociation of the fragment C4H9 rather than any alternative pathways from the parent molecule. Thermodynamic analysis of these pathways has displayed the power of thermodynamic prediction as well as its limitations as it fails to consider kinetic limitations in dissociation reactions.

Dielectrophoresis is an analytical technique which involves electroosmotic flow, electrophoresis, and dielectrophoretic force. These factors, when in correct proportions for a given analyte, allow for dielectrophoretic trapping, otherwise known as dielectrophoretic capture. Non-uniform electric fields are required for this phenomenon, and the device in this trial used to induce such an electric field was a gradient insulator-based design. Similar devices have been previously used to separate or identify a wide variety of analytes within solution. Much of the previous work has been focused on the differences in dielectrophoretic trapping between strains of bacteria, whereas this experiment focused on the differentiation of phenotypes within a single bacterial strain, Staphylococcus aureus isolate 35984. A control sample was tested, as well as a sample heated at 70oC for 15 minutes to induce phenotypic changes. The control sample was found to exhibit dielectrophoretic capture at a given gate at a potential of 800V and higher, whereas the heated sample was not observed to capture at any potential in this experiment, which reached a maximum of 1200V. Notably, neither of the samples were found to capture at or below 600V. The results of this experiment were encouraging, though it is worth noting that several experimental trials failed to produce any noteworthy results. As such, the procedure of this experiment should be refined to increase reproducibility of results.

This paper outlines the design and testing of a z-scan spectrometer capable of measuring the third order refraction index of liquids. The spectrometer underwent multiple redesigns, with each explored in this paper with their benefits and drawbacks discussed. The first design was capable of measuring the third order refraction index for glass, and found a value of 8.43 +- 0.392 x 10^(-16) cm^2/W for the glass sample, with the literature stating glass has a refraction index between 1-100 x 10^(-16) cm^2/W. The second design was capable of measuring the third order refraction index of liquids, and found values of 1.23 $\pm$ 0.121 $\e{-16}$ and 9.43 +- 1.00 x 10^(-17) cm^2/W for water and ethanol respectively, with literature values of 2.7 x 10^(-16) and 5.0 x 10^(-17) cm^2/W respectively. The third design gave inconclusive results due to extreme variability in testing, and and the fourth design outlined has not been tested yet due to time constraints.