The aim of this study was to determine whether resonance frequency analysis can be integrated into the routine clinical evaluation of the initial healing of dental implants. In addition, this study was designed to verify whether there was a correlation between implant stability quotient (ISQ) values, maximum insertion torque values, angular momentum and energy, and to evaluate the importance of different clinical factors in the determination of ISQ values and maximum insertion torque values at implant insertion. Two different implant designs of 81 dental implants in 41 patients were evaluated using ISQ values. Maximum insertion torque values were obtained during the placement procedure. Two new methods were used to calculate the angular momentum developed due to implant installation as well as the energy absorbed by the bone. A linear correlation between ISQ values and maximum insertion torque values at the initial implant surgery was found (P < 0·01). There was a correlation between ISQ values and angular momentum (P < 0·05), although ISQ values and energy did not show a significant linear correlation at the initial surgery (P > 0·05). There was a correlation between maximum insertion torque values, each part's angular momentum, and their energies during installation (P < 0·01). The sequence of the variables that influenced ISQ values was implant location, design, diameter, and gender of the patient. The results of this experiment suggest that both ISQ values and new methods to calculate angular momentum and energy can help to predict implant stability.

This study was undertaken to examine the degradation of TNT, RDX and HMX in a circular photocatalytic reactor with TiO2 as a photocatalyst. We examined the impact of parameters such as the initial concentration, initial pH of solution on rates of photocatalized transformation, and the mineralization. The results showed that photocatalysis is an effective process for the degradation of TNT, RDX and HMX. They could be comoletely degraded in 150 min with 1.0 g/L TiO2 at pH 7. An increase in the photocatalytic degradation of HMX was noticed with decreasing initial HMX. The rates of RDX and HMX degradation were greater in neutral pH than in acidic and alkaline conditions. In case of TNT degradation, the rate of degradation was the fastest at pH 11. Approximately 82% TOC decrease in the TNT degradation was achieved after 150 min, whereas TOC decrease in RDX and HMX was 24% and 59%, respectively. Nitrate, nitrite, and ammonium ions were detected as the nitrogen byproducts from the photocatalysis, and more than 50% of the total nitrogen was recovered as nitrate ion in every explosives.

An activated carbon adsorption model was developed to predict final permeate concentrations of a target trace organic compound (o-dichlorobenzene, DCB) under the variable influent concentration in powdered activated carbon-ultrafiltration (PAC-UF) system for drinking water production. The results were then compared with experimental DCB concentrations both in bulk and permeate. In the adsorption period, the DCB concentrations both in bulk and permeate were always lower than the predicted ones while the permeate concentrations were lower than the bulk ones regardless of membrane materials used and PAC doses. On the other hand, during the desorption period, the experimental values were higher or lower than the predicted ones depending on PAC dose and membrane used. The competitive adsorption and/or desorption of DCB between PAC and membrane itself resulted in this discrepancy, and this trend was more pronounced in a hydrophobic membrane.

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