In this study, an evaluation system that can be used to evaluate the feasibility of developing and supplying hydrothermal energy for the operation of large-scale complex facilities was developed. To this end, this study derived factors to be considered when selecting a location for the use of hydrothermal energy using raw water from multi-purpose dams and regional water supply systems through literature survey and expert interviews. The evaluation indicators derived from this study are divided into four sectors: hydrothermal energy utilization factors, location factors, planning factors, and disaster safety factors, and are composed of 10 mid-level indicators and 34 detailed planning indicators. The relative importance of all factors was derived using the Analytic Hierarchy Process (AHP) technique, and the developed evaluation indicators and relative importance were applied to four multi-purpose dam regions in the country. As a result, it was found that in the development and use of hydrothermal energy utilizing regional raw water supply line the urban planning conditions of the supply site can have a greater impact on the location selection results than the hydrothermal energy development itself. Due to the characteristics of the evaluation indicators developed in this study and their nature as comprehensive indicators, it is believed that the results should be applied to determine the overall adequacy of site selection in the early stages of hydrothermal energy development. In the future, it is believed that it will be necessary to analyze the problems in supplying and operating hydrothermal energy using raw water from multi-purpose dams and regional water resources. Based on the analysis the evaluation system developed in this study is expected to be improved and supplemented.

Nano-sized Zinc selenide (ZnSe) powder was successfully synthesized using Zn and Se precursors in a hydrothermal process. Temperature for the synthesis was varied from 95 oC to 180 oC to evaluate its influence on the microstructural properties of the synthetic particles. ZnSe powder thus fabricated was characterized using various analytical tools such as SEM, XRD, TEM and UV-Vis methods. Two types of ZnSe particles, that is, the precipitated particle and the colloidal particles, were identified in the analysis. The precipitated particles were around 100 nm in average size, whereas the average size of the colloidal particles was around 20 nm. The precipitated particles made at 150 oC and 180 oC were found to be a single phase of ZnSe; however, an inhomogeneous phase was obtained at the lower synthesis temperature of 95 oC, suggesting that the temperature for the synthesis should be over 100 oC. The precipitated particles were inactive in the UV-Vis absorption investigation, whereas the colloidal particles showed that absorptions occurred at 380 nm in the UV-Vis spectrum.

Fe doped TiO2 nanoparticles were prepared under high temperature and pressure conditions by mixture of metal nitrate solution and TiO2 sol. Fe doped TiO2 particles were reacted in the temperature range of 170 to 200˚C for 6 h. The microstructure and phase of the synthesized Fe doped TiO2 nanoparticles were studied by SEM (FE-SEM), TEM, and XRD. Thermal properties of the synthesized Fe doped TiO2 nanoparticles were studied by TG-DTA analysis. TEM and X-ray diffraction pattern shows that the synthesized Fe doped TiO2 nanoparticles were crystalline. The average size and distribution of the synthesized Fe doped TiO2 nanoparticles were about 10 nm and narrow, respectively. The average size of the synthesized Fe doped TiO2 nanoparticles increased as the reaction temperature increased. The overall reduction in weight of Fe doped TiO2 nanoparticles was about 16% up to ~700˚C; water of crystallization was dehydrated at 271˚C. The transition of Fe doped TiO2 nanoparticle phase from anatase to rutile occurred at almost 561˚C. The amount of rutile phase of the synthesized Fe doped TiO2 nanoparticles increased with decreasing Fe concentration. The effects of synthesis parameters, such as the concentration of the starting solution and the reaction temperature, are discussed.

1-D ZnO nanowires have been attractive for their peculiar properties and easy growth at relatively low temperature. The length, diameter, and density of ZnO nanowires were determined by the several synthetic parameters, such as PEI concentration, growth time, temperature, and zinc salt concentration. The ZnO nanowires were grown on the<001> oriented seed layer using the hydrothermal process with zinc nitrate and HMTA (hexamethylenetetramine) and their structure and optical properties were characterized. The morphology, length and diameter of the nanowires were strongly affected by the relative and/or absolute concentration of Zn2+ and OH-1 and the hydrothermal temperature. When the concentrations of the zinc nitrate HMTA were the same as 0.015 M, the length and diameter of the nanowires were 1.97μm and 0.07μm, respectively, and the aspect ratio was 28.1 with the preferred orientation along the<001> direction. XRD and TEM results showed a high crystallinity of the ZnO nanowires. Optical measurement revealed that ZnO nanowires emitted intensive stimulated UV at 376 nm without showing visible emission related to oxygen defects.

ZnO nanorods for gas sensors were prepared by a hydrothermal method. The ZnO gas sensors were fabricated on alumina substrates by a screen printing method. The gas-sensing properties of the ZnO nanorods were investigated for CH4 gas. The effects of growth time on the structural and morphological properties of the ZnO nanorods were investigated by X-ray diffraction and scanning electron microscope. The XRD patterns of the nanocrystallized ZnO nanorods showed a wurtzite structure with the (002) predominant orientation. The diameter and length of the ZnO nanorods increased in proportion to the growth time. The sensitivity of the ZnO sensors to 5 ppm CH4 gas was investigated for various growth times. The ZnO sensors exhibited good sensitivity and rapid response-recovery characteristics to CH4 gas, and both traits were dependent on the growth time. The highest sensitivity of the ZnO sensors to CH4 gas was observed with the growth time of 7 h. The response and recovery times were 13 s and 6 s, respectively.

Hydrothermal carbonization (HTC) is a highly effective technique for treating lignocellulosic biomass and organic waste of various shapes and moisture content. The solid product of HTC is friable, hydrophobic, and increased in mass and energy densification compared to the raw biomass. also solid product is similar regardless of the type of biomass used. A liquid solution of five carbon and six carbon sugars, along with various organic acids and 5-HMF, is also produced from HTC of lignocellulosic biomass. The gaseous phase product consists mostly of CO2. Solid product has the similar characteristics to low rank coal. The solid fuel characteristics of feedstock was increased with reaction temperature and time via HTC process. However, mass yield was decreased with increasing temperature and time. Therefore, it is necessary to optimize the reaction temperature and time for HTC. The HTC process produces the solid product and a large amount of water. Thus the reuse or treatment techniques of liquid product is necessary. Therefore, potential of biological treatment of HTC liquid product was evaluated.