• Clean Technology
• /
• v.26 no.4
• /
• pp.311-320
• /
• 2020

In this study, the photocatalytic degradation of rhodamine B (RhB), methyl orange (MO) and methylene blue (MB) was carried out under visible light irradiation using CdS and CdZnS/ZnO photocatalysts prepared by a simple precipitation method. This study focused on examining the effect of physicochemical properties of dye and photocatalyst on the reaction pathway of photocatalytic degradation. The prepared photocatalysts were characterized by XRD, UV-vis DRS and XPS. Both the CdS and CdZnS/ZnO photocatalysts exhibit an excellent absorption in the visible light and the UV light regions. It was observed that the photocatalytic degradation of MO proceeds via the same reaction mechanism on both the CdS and CdZnS/ZnO photocatalysts. However, the photocatalytic degradation of RhB and MB was found to proceed through a different reaction pathway on the CdS and CdZnS/ZnO catalysts. It is interesting to note that MB dimer was formed on the CdS catalyst at the beginning of the photocatalytic reaction, while the MB monomer was degraded during the overall photocatalytic reaction on CdZnS/ZnO. The above results may be mainly ascribed to the difference of band edge potential of the conduction band in the CdS and CdZnS/ZnO semiconductors and the adsorption property of dye on the catalysts.

• KSCE Journal of Civil and Environmental Engineering Research
• /
• v.29 no.1A
• /
• pp.75-84
• /
• 2009

The present study assesses the chloride threshold level for corrosion of steel in concrete by examining the properties of four different binders used for blended concrete in terms of chloride binding, buffering of cement matrix to a pH fall and the corrosion behaviour. As binders, ordinary Portland cement (OPC), 30% pulverised fuel ash (PFA), 60% ground granulated blast furnace slag (GGBS) and 10% silica fume (SF) were used in a concrete mix. Testing for chloride binding was carried out using the water extraction method, the buffering of cement matrix was assessed by measuring the resistance to an artificial acidification of nitric acid, and the corrosion rate of steel in mortar with chlorides in cast was measured at 28 days using an anodic polarisation technique. Results show that the chloride binding capacity was much affected by $C_{3}A$ content and physical adsorption, and its order was 60% GGBS>30% PFA>OPC>10% SF. The buffering of cement matrix to a pH fall was varied with binder type and given values of the pH. From the result of corrosion test, it was found that the chloride threshold ranged 1.03, 0.65, 0.45 and 0.98% by weight of cement for OPC, 30% PFA, 60% GGBS and 10% SF respectively, assuming that corrosion starts at the corrosion rate of $0.1-0.2{\mu}A/cm^{2}$. The mole ratio of [$Cl^{-}$]:[$H^{+}$], as a new presentation of the chloride threshold, indicated the value of 0.008-0.009, irrespective of binder, which would be indicative of the inhibitive characteristic of binder.

• Applied Chemistry for Engineering
• /
• v.21 no.2
• /
• pp.183-187
• /
• 2010

Activated carbons (ACs) have been prepared from pitch by the combination of a chemical oxidation with different $H_2O_2$ concentrations i.e., 5, 15, and 25 wt% and a chemical activation with KOH at a constant KOH/pitch ratio of 3/1. The influence of $H_2O_2$ solution on the microporous properties of the pitch and the final activated carbons were invested using XRD, FT-IR, XPS, $N_2$-adsorption, and SEM. XRD indicated that the value of interplanar distance $d_{002}$ increased by chemical oxidation. FT-IR and XPS results showed that the chemical oxidation promoted the formation of surface oxygen functionalities. Also, the specific surface area of the resulting ACs was increased with increasing the concentration of $H_2O_2$ chemical oxidation and showed a maximum value of $2111m^2/g$ at 25 wt% $H_2O_2$ concentration.

• Applied Chemistry for Engineering
• /
• v.31 no.1
• /
• pp.108-114
• /
• 2020

In this study, NH₃-selective catalytic oxidation (SCO) efficiencies according to calcination/reduction conditions were compared when preparing various Ru[1]/TiO₂ catalysts. The Ru[1]/TiO₂ red catalyst had better NH₃ conversion and NH₃ to N₂ conversion than those of Ru[1]/TiO₂ cal. Physico-chemical properties of Ru[1]/TiO₂ catalysts were confirmed by Brunauer Emmett Teller (BET), X-ray diffraction (XRD), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS) and temperature programmed reduction (H₂-TPR) analyses, and the properties were shown to affect the dispersion and surface adsorption oxygen species (O_β) ratio of the active metal.

• Journal of Soil and Groundwater Environment
• /
• v.22 no.1
• /
• pp.27-32
• /
• 2017

Cesium (Cs) generated by nuclear accidents is one of the most hazardous radionuclides because of its gamma radiation and long half-life. Especially, when Cs is exposed on the soil environments, Cs is mainly adsorbed on the topsoil and is strongly combined with tiny soil particle including clay minerals. The adsorption of Cs onto soil can vary depending on various physicochemical properties of soil. In this study, the adsorption characteristics between soil and Cs were investigated according to various physicochemical properties of soil including organic matter contents, cation exchange capacity (CEC), soil particle size, and the types of clay minerals. Soil organic matter inhibited the adsorption of Cs onto the soil because organic matter was blocking the soil surface. In addition, it was estimated that the CEC of the soil influenced the adsorption of Cs onto the soil. Moreover, more Cs was adsorbed as the soil particles size decreased. It was estimated that Cs was mostly adsorbed onto the topsoil, this is related to the clay mineral. Therefore, soil organic matter, CEC, soil particle size, and clay minerals are considered the key factors that can influence the adsorption characteristics between soil and Cs.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
• /
• 2008.11a
• /
• pp.281-281
• /
• 2008

최근 높은 비표면적, 우수한 결정성, 나노스케일의 크기 등 다양한 물리 화학적 특성을 지닌 1차원 나노구조체를 이용한 가스센서 연구가 활발히 진행되고 있다. 가스센서는 네트워크 된 나노선들 이용하여 벌크, 박막 보다 극대화된 비표면적으로 가스 감도와 반응 속도를 향상시킬 수 있었다. 촉매 첨가를 위해 Acetylacetone 용액 7 ml에 10 mM이 되도록 Pt 분말을 첨가하여 촉매용액을 제조하였다. 마이크로피펫을 이용하여 미량을 센서의 감응체 부문에 뿌려 대기 중에서 건조한 후 센서의 감도를 측정하였다. 측정은 $250^{\circ}C$에서 일산화탄소 가스 500 ppm의 가스농도로 촉정하였을 때 촉매가 첨가된 센서가 70% 이상의 개선된 감도를 나타내었다. 이는 나노선에 분산된 촉매에 주입되는 가스가 흡착되고 다시 표면의 산소와 반응하여 전기전도도를 변화시키는 것으로 보인다. 첨가된 촉매에 대한 영향을 분석하기 위해 AES, XRD, FT-IR, TEM 등의 분석을 실시하였다.

• Journal of Korean Society of Water and Wastewater
• /
• v.22 no.4
• /
• pp.467-473
• /
• 2008

Natural organic matter (NOM) removal by physico-chemical adsorption and biological oxidation was investigated in five slow sand filters with different media depths. Non-purgeable dissolved organic carbon(NPDOC) and $UV_{254}$ absorbance were measured to evaluate the characteristics of NOM removal at different filter depths. Removal efficiency of NOM was in the range of 10-40% throughout the operation time. At start-up of the filters packed with clean sand media, NOM was probably removed by physico-chemical adsorption on the surface of sand through the overall layer of filter bed. However, when Schumutzdecke layer was built up after 30 days operation, the major portion of NPDOC was removed by biological oxidation and/or bio-sorption in lower depth above 50 mm. NOM removal rate in the upper 50 mm filter bed was $0.82hr^{-1}$. It was about 20 times of the rate($0.04hr^{-1}$) in the deeper filter bed. Small portion of NPDOC could be removed in the deeper filter bed by both bio-sorption and biodegradation. SEM analysis and VSS measurement clearly showed the growth of biofilm in the deeper filter bed below 500 mm, which possibly played an important role in the NOM removal by biological activity besides the physco-chemical adsorption mechanism

• Journal of Korean Society on Water Environment
• /
• v.33 no.6
• /
• pp.689-695
• /
• 2017

This study was carried out to investigate the physicochemical and adsorptive characteristics of black carbon (BC) materials for cesium in case of severe nuclear accidents. The BC was prepared with a xylem of oak and pine trees incompletely combusted with different ramp rate and final temperature. Carbon (C), hydrogen (H) and oxygen (O) atomic ratios, BET, pore structure, and zeta potential were characterized for the produced BC. A low cesium concentration ($C_w{\approx}10^{-7}M$) was used for sorption batch experiments. The H/C and O/C ratios of BC decreased with the increase of final temperature, which indicates a carbonization of the wood materials regardless of ramp rate and tree species. However, SEM images showed different pore structures depending on tree species such as steric and plate-like for oak-BC and pine-BC, respectively. The greatest sorption distribution coefficients of $K_{d,Cs}{\approx}1,200{\sim}1,800L\;kg^{-1}$ were observed for the oak-BC produced at $400^{\circ}C$, while comparatively low $K_{d,Cs}$ < $100L\;kg^{-1}$ for pine-BC. In addition, the sorption capabilities of BC declined with the increase of combustion temperature up to $600^{\circ}C$, because high temperature destroyed surface functionalities with the rise of ash components in the BC. Therefore, the sorption processes of BC for radioactive cesium are predominantly controlled by final production temperature of BC as well as raw materials (e.g., tree species).

• Journal of Korean Society of Environmental Engineers
• /
• v.37 no.5
• /
• pp.285-292
• /
• 2015

In this study, we were clearly identify the behaviour characteristics on particle size distribution of a condensing species by injection condition of HMDS (Hexa Methyl Di-Silazane, silica precursor that is one of liquid adsorbents) to remove condensing gaseous species as using pyroligneous liquor generated during carbonization process of biomass as precursor of condensing gaseous species. When using HMDS to remove the condensing gaseous species by growth machanism of particles, we could be controlled properly particles size such as amount of adsorbent injection, residence time, heating temperature and MFC flux. Especially, in case of using the silica precursor, in consideration of the physical and chemical properties of the boiling point, the specific gravity and the molecular weight, we found that the condensing species could be effectively controlled by particles granulation.

• Journal of the Korean Applied Science and Technology
• /
• v.33 no.1
• /
• pp.129-135
• /
• 2016

CO oxidation was performed with Cu-Mn and Cu-Zn co-precipitated catalysts as differential precipitant, metal ratio and calcination temperature. The effects of differential metal mole ratio and calcination temperature in mixed metal oxide catalyst were investigated with CO oxidation reaction. Physiochemical properties were studied by XRD, $N_2$ sorption and SEM. 2Cu-1Mn with $Na_2CO_3$ catalyst calcined at $270^{\circ}C$ has a large surface area $43m^2/g$ and the best activity for CO oxidation. $Cu_{0.5}Mn_{2.5}O_4$ in XRD peak shows the lower activity than others. The catalytic activity over the catalyst calcined $270^{\circ}C$ displayed the highest conversion, and it was better activity comparing with Pt catalysts CO conversion.