• The Journal of Korean Academy of Prosthodontics
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• v.43 no.3
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• pp.363-378
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• 2005

Statement of problem. Hydroxyapatite(HA) coated titanium surfaces have not yet showed the reliable osseointegration in various conditions. Purpose. This study was aimed to investigate microstructures, chemical composition, and surface roughness of the surface coated by the hydrothermal method and to evaluate the effect of hydrothermal coating on the cell attachment, as well as cell proliferation. Material and Methods. Commercially pure(c.p.) titanium discs were used as substrates. The HA coating on c.p. titanium discs by hydrothermal method was performed in 0.12M HCl solution mixed with HA(group I) and 0.1M NaOH solution mixed with HA(group II). GroupⅠ was heated at 180 $^{\circ}C$ for 24, 48, and 72 hours. GroupⅡ was heated at 180 $^{\circ}C$ for 12, 24, and 36 hours. And the treated surfaces were evaluated by Scanning electron microscopy(SEM), Energy dispersive X-ray spectroscopy(EDS), X-ray photoelectron spectroscopy(XPS), X-ray diffraction method(XRD), Confocal laser scanning microscopy(CLSM). And SEM of fibroblast and 3-(4,5- dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide(MTT) assay were used for cellular responses of the treated surfaces. Results. The color of surface changed in both groups after the hydrothermal process. SEM images showed that coating pattern was homogeneous in group II, while inhomogeneous in group I. H72 had rosette-like precipitates. The crystalline structure grew gradually in group II, according to extending treatment period. The long needle-like crystals were prominent in N36. Calcium(Ca) and phosphorus(P) were not detected in H24 and H48 in EDS. In all specimens of group II and H72, Ca was found. Ca and P were identified in all treated groups through the analysis of XPS, but they were amorphous. Surface roughness did not increase in both groups after hydrothermal treatment. The values of surface roughness were not significantly different between groups I and II. According to the SEM images of fibroblasts, cell attachments were oriented and spread well in both treated groups, while they were not in the control group. However, no substantial amount of difference was found between groups I and II. Conclusions. In this study during the hydrothermal process procedure, coating characteristics, including the HA precipitates, crystal growth, and crystalline phases, were more satisfactory in NaOH treated group than in HCl treated group. Still, the biological responses of the modified surface by this method were not fully understood for the two tested groups did not differ significantly. Therefore, more continuous research on the relationship between the surface features and cellular responses seems to be in need.

• Korean Journal of Materials Research
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• v.20 no.5
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• pp.262-266
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• 2010

ZnO nanostructures were grown on an Au seed layer by a hydrothermal method. The Au seed layer was deposited by ion sputter on a Si (100) substrate, and then the ZnO nanostructures were grown with different precursor concentrations ranging from 0.01 M to 0.3M at $150^{\circ}C$ and different growth temperatures ranging from $100^{\circ}C$ to $250^{\circ}C$ with 0.3 M of precursor concentration. FE-SEM (field-emission scanning electron microscopy), XRD (X-ray diffraction), and PL (photoluminescence) were carried out to investigate the structural and optical properties of the ZnO nanostructures. The different morphologies are shown with different growth conditions by FE-SEM images. The density of the ZnO nanostructures changed significantly as the growth conditions changed. The density increased as the precursor concentration increased. The ZnO nanostructures are barely grown at $100^{\circ}C$ and the ZnO nanostructure grown at $150^{\circ}C$ has the highest density. The XRD pattern shows the ZnO (100), ZnO (002), ZnO (101) peaks, which indicated the ZnO structure has a wurtzite structure. The higher intensity and lower FWHM (full width at half maximum) of the ZnO peaks were observed at a growth temperature of $150^{\circ}C$, which indicated higher crystal quality. A near band edge emission (NBE) and a deep level emission (DLE) were observed at the PL spectra and the intensity of the DLE increased as the density of the ZnO nanostructures increased.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.30 no.3
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• pp.91-95
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• 2020

In this study, we report a hydrothermal synthesis in which BaTiO₃ nanoparticles (NPs) with enhanced size uniformity and dispersibility are synthesized by increased time and temperature, increasing nucleation and diffusion rates. The formation process of an uniform size of 20 nm BaTiO₃ NPs, which has not been extensively researched, was optimized through hydrothermal synthesis at 180℃. Simultaneous increase in the nucleation rate of TiO₂ and diffusion length of Ba²⁺ ions, resulting from a higher temperature, allowed for the synthesis of BaTiO₃ NPs (20 nm) with significantly enhanced size-uniformity. The size and crystallinity of BaTiO₃ NPs which exhibit excellent dispersibility in hexane solvent were investigated using transmission electron microscopy and X-ray diffraction. The results presented herein provide insights into improving the size uniformity and dispersibility of BaTiO₃ NPs by hydrothermal synthesis for applications to variety of electronic devices.

• Korean Journal of Microbiology
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• v.48 no.1
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• pp.42-47
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• 2012

Hydrothermal vents (HTV) provide special environments for evolution of lives independent on solar energy. HTV samples were gained from Tofua arc trench in Tonga, South Pacific. We investigated archaeal diversity enriched using combinations of various electron donors (yeast extract and $H_2$) and electron acceptors [Iron (III), elemental sulfur ($S^0$) and nitrate. PCR amplification was performed to detect archaeal 16S rRNA genes after the cultures were incubated $65^{\circ}C$ and $80^{\circ}C$ for 2 weeks. The cultures showing archaeal growth were transferred using the dilution-to-extinction method. 16S rRNA gene PCR-Denaturing Gradient Gel Electrophoresis was used to identify the enriched archaea in the highest dilutions where archaeal growth was observed. Most of cultured archaea belonged to genus of Thermococcus (T. alcaliphilius, T. litoralis, T. celer, T. barossii, T. thoreducens, T. coalescens) with 98-99% 16S rRNA gene similarities. Interestingly, archaeal growth was observed in the cultures with Iron (III) and nitrate as an electron acceptor. It was supposed that archaea might use the elemental sulfur generated from oxidation of the reducing agent, sulfide. To cultivate diverse archaea excluding Thermococcus, it would be required to use other reducing agents instead of sulfide.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2009.11a
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• pp.238-238
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• 2009

In this work, we investigated the effect of the Zn complex concentration and growth temperature on the growth of ZnO nanorod by hydrothermal method. The ZnO nanorods were performed at condition of the various Zn complex concentration and growth temperature, 0.02 ~ 0.08 M and 60 ~ 80 $^{\circ}C$, respectably. We found from the SEM results that the diameter and length of ZnO nanorods were with increasing the growth temperature and Zn complex concentration. However, the growth condition in the two parameters wasmore than sensitive compared to Zn complex concentration on increasing the growth rate. From photoluminescence(PL) analysis, the strong band-edge emission for ZnO nanorod grown at 80 $^{\circ}C$ with 0.08 M indicated the fine crystallinity. Therefore, the diameter and length of ZnO nanorods have been able to control through the control of front growth parameters. Also, these ZnO nanorods grown low temperature will be available as building block for transparence flexible device applications.

• Proceedings of the Korean Ceranic Society Conference
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• 2003.10a
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• pp.28.2-28
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• 2003

• Proceedings of the Korean Ceranic Society Conference
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• 2003.10a
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• pp.91.2-91
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• 2003

• Applied Chemistry for Engineering
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• v.10 no.4
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• pp.509-514
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• 1999

In Preparing $BaTiO_3$ powder under hydrothermal conditions, effects of reaction period feedstock concentration and mixing rate on crystallinity, mean size and size distribution of particles were studied. Experimental results showed that the particle size became smaller with its narrow distribution as the reaction period and mixing rate increased, but feedstock concentration decreased in contrast with the results based on the classical nucleation-growth model. From these results, $BaTiO_3$ particles seem to be prepared hydrothermally through a multiple reaction procedure that includes dissolution, precipitation, hydrolysis-condensation, aggregation, diffusion and transformation.

• Bulletin of the Korean Chemical Society
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• v.25 no.9
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• pp.1341-1345
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• 2004

We developed a novel synthesis strategy of titania nanowire arrays by employing simple hydrothermal reaction and ion-exchange reaction techniques. Hydrothermal reactions of metallic titanium powder with $H_2O_2$ in a 10 M NaOH solution produced a new sodium titanate compound, $Na_2Ti_6O_{13}{\cdot}xH_2O$ (x~4.2), as arrays of nanowires of lengths up to 1 mm. Acid-treatment followed by calcination of this material produced arrays of highly crystalline anatase nanowires as evidenced by x-ray diffraction, Raman spectroscopy, and transmission electron microscopy studies. In both cases of sodium titanate and anatase, the nanowires have exceptionally large aspect ratios of 10,000 or higher, and they form arrays over a large area of $1.5 {\times} 3 cm^2$. Observations on the reaction products with varied conditions indicate that the array formation requires simultaneously controlled formation and crystal growth rates of the $Na_2Ti_6O_{13}{\cdot}xH_2O$ phase.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.8 no.1
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• pp.42-48
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• 1998

Synthesis of PLT($Pb_{1-X}La_{2X/3}TiO_3$, x=0.1~0.3) powders was carried out by hydrothermal method. Optimal conditions for synthesis were $250^{\circ}C$ of reaction temperature, 8M-KOH solution of hydrothermal solvent and 12 hrs reaction time, and the monolithic $Pb_{1-X}La_{2X/3}TiO_3$ particles were obtained with the composition of x$\leq$0.2. The tetragonality(c/a) and the phase transition temperature were decreased by the increment of the $La_2O_3$ contents in PLT solid solutions, and the Curie temperature of the $Pb_{1-X}La_{2X/3}TiO_3$(x=0.2) was $400^{\circ}C$. The shape of the synthesized particles were nearly spherical and the size was in the 20~200 nm range.