• Bulletin of the Korean Chemical Society
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• v.26 no.4
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• pp.563-568
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• 2005

The Pt/C and Pd/C catalysts were prepared from conventional chloride precursors by adsorption or precipitation-deposition methods. Their activities for hydrogenation reactions of cyclohexene and acetophenone were compared with those of commercial catalysts. The Pt/C and Pd/C catalysts obtained from the adsorption procedure reveal higher hydrogenation activity than commercial catalysts and the catalysts prepared by the precipitation-deposition method. Their improved performances are attributed to the decreased metal crystallite sizes of Pt or Pd formed on the active carbon support upon the adsorption of the precursors probably due to the same negative charges of the chloride precursor and the carbon support. Under the preparation conditions studied, the reduction of the supported catalysts using borohydrides in liquid phase is superior to a gas phase reduction by using hydrogen in the viewpoint of particle size, hydrogenation activity and convenience.

• Advances in nano research
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• v.6 no.1
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• pp.1-19
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• 2018

Iron oxide nanoparticles excite researcher interest in biomedical applications due to their low cost, biocompatibility and superparamagnetism properties. Magnetic iron oxide especially magnetite ($Fe_3O_4$) possessed a superparamagnetic behaviour at certain nanosize which beneficial for drug and gene delivery, diagnosis and imaging. The properties of nanoparticles mainly depend on their synthesis procedure. There has been a massive effort in developing the best synthetic strategies to yield appropriate physico-chemical properties namely co-precipitation, thermal decomposition, microemulsions, hydrothermal and sol-gel. In this review, it is discovered that magnetite nanoparticles are best yielded by co-precipitation method owing to their simplicity and large production. However, its magnetic saturation is within range of 70-80 emu/g which is lower than thermal decomposition and hydrothermal methods (80-90 emu/g) at 100 nm. Dimension wise, less than 100 nm is produced by co-precipitation method at $70^{\circ}C-80^{\circ}C$ while thermal decomposition and hydrothermal methods could produce less than 50 nm but at very high temperature ranging between $200^{\circ}C$ and $300^{\circ}C$. Thus, co-precipitation is the optimum method for pre-compliance magnetite nanoparticles preparation (e.g., 100 nm is fit enough for biomedical applications) since thermal decomposition and hydrothermal required more sophisticated facilities.

• Journal of Korean Society for Atmospheric Environment
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• v.14 no.6
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• pp.589-598
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• 1998

This study was conducted to investigate the chemical characteristics of Precipitation at Seoul, Yangpyong, Hongchon and Inje in the central part of Korean peninsula during the period from March 1994 to November 1997. The precipitation samples were collected by automatic wet-only sampler. The samples were analyzed for major anions (SO42-, NO3-, Cl-, F-) and cations(NH4+, Ca2+, Mg+, Na+, K+), in addition to acidity and electrical conductivity. The analytical instrument for water soluble ionic components was ion chromatography. The volume - weighted mean PH were 4.73, 4.87, 4.89 and 4.81 at Seoul, Yangpyong, Hongchon and Inje, respectively. The sums of cation concentrations was slightly greater than the sums of anion concentrations. Also, the highest ion component was SO42- in anions and NH4+ in cations. The mean equivalent ratios of SO42- to NO3- were found by 2.96, 2.71, 2.43 and 2.25 at Seoul, Yangpyong, Hongchon and Inje, respectively. The factor analysis was conducted in order to make the large and diverse data set as manageable levels and to qualitatively examine the relationship between the variables. It showed that major sources of pollutants in precipitation were from the anthropogenic in Seoul, the natural in Hongchon, and the anthropogenic and natural in Yangpyong and Inje.

• Microbiology and Biotechnology Letters
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• v.40 no.2
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• pp.157-162
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• 2012

In this study, we have for the first time applied increased surface area fractional precipitation in order to decrease the particle size of the anticancer agent paclitaxel from plant cell cultures. When compared with the case where no surface area increasing material was employed, the addition of ion exchange resin as a surface area increasing material resulted in a considerable decrease in the size of the paclitaxel precipitate. When ion exchange resin was used, the paclitaxel particles were four to five times smaller, having less than a 20 ${\mu}m$ radius, than those obtained in the absence of ion exchange resin. This is presumably because the growth of paclitaxel particles was impeded by the addition of ion exchange resin. The size of the paclitaxel precipitate also depended on the material used to increase the surface area, a result considered to be due to differences in the affinity between the particular ion exchange resin used and the paclitaxel particles. The yield of paclitaxel was significantly improved when ion exchange resin was used as a material to increase surface area. Paclitaxel, with a reduced particle size due to the addition of a surface area increasing material during the fractional precipitation process, is believed to be particularly useful for practical applications of the drug.

• Korean Journal of Materials Research
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• v.12 no.12
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• pp.947-954
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• 2002

HCl concentration and reaction time are the decisive factors in determining the structure of precipitates in the process of synthesis of $TiO_2$ particles from aqueous $TiOCl_2$ solution by precipitation and the volumetric proportion of brookite phase in $TiO_2$ particles can be controlled by these two factors. As reaction rate increases with increase of reaction temperature, the reaction time, at which maximum volumetric proportion of brookite phase in $TiO_2$ particles was obtained, was reduced. The brookite was transformed directly to rutile phase with only increase of reaction time. And precipitation was delayed with increase of HCl concentration because the amount of $H_2$O, which is necessary source of oxygen for conversion of $Ti^{+4}$ to $TiO_2$, was relatively reduced with increase of that. Brookite in the mixture phase powder was finally transformed to rutile phase via anatase through heat-treatment.

• Bulletin of the Korean Chemical Society
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• v.25 no.8
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• pp.1156-1160
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• 2004

The technique of an on-line preconcentration by the direct sulfide precipitation has been developed. Sn was homogeneously precipitated by sulfide, which was generated in situ from the hydrolysis of thioaceteamide. Precipitate was collected on a filter in the line and dissolved out instantaneously by KOH to be sent to an ICP. The enrichment factor was 4 with the sampling speed of 15/hr for 1.0 mL of sample. It was increased to more than 40 times when the sampling volume was increased to 10 mL with the sampling speed of 5/hr. $Sn^{2+}/Sn^{4+}$ could be separately determined with the on-line precipitation technique. The method was applied to the analysis of NIST SRM 1566 Oyster sample and yielded good agreement with the certified value.

• Journal of Korean Society for Atmospheric Environment
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• v.10 no.3
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• pp.159-169
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• 1994

This paper describes the process of acidic precipitation from the atmosphere to the ground water, The net deposition of wet precipitation to the ground surface is obtained by subtracting the interception loss due to plant leaves and evaporation from the amount of total precipitation. As the water immerses through the vegetation and the different soil layers the various chemical reactions take place. The relationship between the acidic precipitation by increasing industrial emissions and the soil acidification mechanism is discussed. The report focuses on the buffering action that involves the proton budget in soil and rocks. Based on the soil constituents, the six buffer ranges of the soil are classified and each buffering process is illustrated. In addition, the Possibility of the contamination of drinking-water reservoirs by continuous acid burden is emphasized.

• 한국생물공학회:학술대회논문집
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• 2005.10a
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• pp.560-561
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• 2005

• 한국생물공학회:학술대회논문집
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• 2005.10a
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• pp.539-540
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• 2005

• Bulletin of the Korean Chemical Society
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• v.28 no.5
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• pp.721-722
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• 2007