Perchlorate reduction using electrochemically induced pitting corrosion of zero-valent titanium

Perchlorate is a threat to public health through water but also food. However, there is no effective chemical treatment process which can destroy perchlorate found in groundwater and surface water. Thus, there is growing interest in developing effective technologies, especially chemical treatments, to completely destroy trace levels of perchlorate present in drinking and groundwater. The research on perchlorate reduction by zero-valent titanium (Ti(0)) showed that perchlorate was effectively reduced to chloride using electrochemically developed pitting corrosion on Ti(0). Perchlorate reduction was believed to be caused by an active reductant (dissolved Ti(II)) during the pitting corrosion of Ti(0). The rate of perchlorate reduction was independent on the imposed potential as long as the potential was maintained above the pitting potential of Ti(0), but it was proportional to the applied current. The perchlorate reduction on the pitting developed Ti(0) was inhibited by the presence of chloride and bromide. Inhibition mechanism of perchlorate reduction inhibition was believed to be caused either by competitive adsorption of aggressive anions on bare Ti(0) surface or Ti(II) consumption by electrochemically produced chlorine. Kinetic models were developed based surface coverage of aggressive anions on bare Ti(0) and Ti(II) oxidation by chlorine. These kinetic models supported the perchlorate concentration change in the solution, but Ti(II) consumption model was not able to predict chloride concentration due to insufficient information describing complex nature of pitting on Ti(0). These results shown in this research demonstrate that pitting corrosion developed Ti(0) has the capability to chemically reduce perchlorate present in natural water and engineered systems as well as possible problems associated with electric input. This research may be a starting point for development of a new treatment process that applies titanium or titanium metal ions as a chemical reductant to abate contaminants present in natural and engineering systems. Further developments can be achieved by alloying titanium metal with other metals such as iron and aluminum, and finding a methodology producing stable Ti(II) in ambient conditions

The application of eccentric rotating cylinder apparatus for the improved study of particle coagulation

Concentric rotating cylinder and turbulent mixing devices have been frequently used in studying mixing and particle coagulation. However, these apparatus develop simple laminar flow (concentric rotating cylinders) or do not have well-defined flow (turbulent mixing devices). In this work, the eccentric rotating cylinder apparatus was investigated to find applicability for the improved study of coagulation based on the modified analytical solution of Ballal and Rivlin. Various eccentricity ratios, rotation speeds and viscosities were simulated to obtain optimum operating conditions. Inertial forces working on the fluid increased as the eccentricity ratio and rotation speed increase. As inertial forces increase, the eddy developed in wide clearance was more skewed in the direction of rotation. Both root-mean-square velocity gradient and average principal strain-rate, were increased by increasing eccentricity ratio. avaerage principal strain-rate were linearly increased as rotation speed increases, which suggested that average prinipal strain-rate can properly represent mixing intensity. Comparison of average principal strain-rate and RMS velocity gradient revealed that RMS velocity gradient overestimated mixing intensity and its error increased as eccentricity ratio increases. This study showed that the eccentric rotating cylinder apparatus has a non-uniform velocity distribution with well-defined fluid dynamics. Therefore, the eccentric rotating cylinder apparatus can be applicable as a model flocculator. However, in order to achieve reliable model predictability, the fluid Reynolds number must be below 200

SYSTEMATICS OF RYDBERG SERIES OF DIATOMIC MOLECULES AND CORRELATION DIAGRAMS

Rydberg states are studied for H$_{2}$, Li$_{2}$, HeH, LiH and BeH using the multi-reference configuration interaction (MRCI) method. The systematics and regularities of the physical properties such as potential energies curves (PECs), quantum defect curves, permanent dipole moment and transition dipole moment curves of the Rydberg series are studied. They are explained using united atom perturbation theory by Bingel and Byers-Brown, Fermi model, Stark theory, and Mulliken's theory. Interesting mirror relationships of the dipole moments are observed between $l$-mixed Rydberg series, indicating that the members of the $l$-mixed Rydberg series have dipole moments with opposite directions, which are related to the reversal of the polarity of a dipole moment at the avoided crossing points. The assignment of highly excited states is difficult because of the usual absence of the knowledge on the behaviors of potential energy curves at small internuclear separation whereby the correlation between the united atom limit and separated atoms limit cannot be given. All electron MRCI calculations of PECs are performed to obtain the correlation diagrams between Rydberg orbitals at the united-atom and separated atoms limits