• 제목/요약/키워드: Colloid

검색결과 428건 처리시간 0.022초

우라닐 가수분해물의 용해도 연구 (Solubility Studies of Uranyl Hydrolysis Precipitates)

  • 박용준;표형렬;김원호;전관식
    • 대한화학회지
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    • 제40권9호
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    • pp.599-606
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    • 1996
  • 서로 다른 pH 조건에서 생성한 우라닐 가수분해물의 용해도에 미치는 지하수 성분의 영향을 측정하였다. 우라닐 가수분해 침전물 pH 6.4 및 9.7에서 제조하였다. 편마암 층에서 채취한 지하수로부터 무기 및 유기콜로이드를 제거한 분리지하수, 채취지하수의 분석성분과 동일한 조성을 가지는 합성지하수, 그리고 0.1 M NaCl 수용액에서의 용해도에 미치는 pH의 영향을 측정하였다. 또한 채취지하수에서 상대적으로 다량 존재하는 음이온 및 양이온의 영향을 측정하였다. 지하수에서의 우라닐 가수분해 침전물의 용해도는 0.1 M NaCl 용액에서보다 약 100배 정도 큰 것으로 나타났다. X-선 회절분석 결과는 높은 pH에서 제조한 우라닐 가수분해 침전물이 낮은 pH에서 제조한 것보다 낮은 결정화도와 높은 용해도를 보였다.

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Effect of citrate coated silver nanoparticles on biofilm degradation in drinking water PVC pipelines

  • Nookala, Supraja;Tollamadugu, Naga Venkata Krishna Vara Prasad;Thimmavajjula, Giridhara Krishna;Ernest, David
    • Advances in nano research
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    • 제3권2호
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    • pp.97-109
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    • 2015
  • Citrate ion is a commonly used reductant in metal colloid synthesis, undergoes strong surface interaction with silver nanocrystallites. The slow crystal growth observed as a result of the interaction between the silver surface and the citrate ion makes this reduction process unique compared to other chemical and radiolytic synthetic methods. The antimicrobial effects of silver (Ag) ion or salts are well known, but the effects of citrate coated Ag nanoparticles (CAgNPs) are scant. Herein, we have isolated biofilm causative bacteria and fungi from drinking water PVC pipe lines. Stable CAgNPs were prepared and the formation of CAgNPs was confirmed by UV-visible spectroscopic analysis and recorded the localized surface plasmon resonance of CAgNPs at 430 nm. Fourier transform infrared spectroscopic analysis revealed C=O and O-H bending vibrations due to organic capping of silver responsible for the reduction and stabilization of the CAgNPs. X-ray diffraction micrograph indicated the face centered cubic structure of the formed CAgNPs, and morphological studies including size (average size 50 nm) were carried out using transmission electron microscopy. The hydrodynamic diameter (60.7 nm) and zeta potential (-27.6 mV) were measured using the dynamic light scattering technique. The antimicrobial activity of CAgNPs was evaluated (in vitro) against the isolated fungi, Gram-negative and Gram-positive bacteria using disc diffusion method and results revealed that CAgNPs with 170ppm concentration are having significant antimicrobial effects against an array of microbes tested.

비닐아세테이트/알킬아크릴레이트계 에멀젼 공중합과 등온 열분해 특성 (Characteristics of Isothermal Analysis and Emulsion Copolymerization of Vinyl Acetate/Alkyl Acrylate)

  • 조대훈;최성일;설수덕
    • 접착 및 계면
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    • 제13권2호
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    • pp.64-72
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    • 2012
  • 비닐아세테이트와 알킬아크릴레이트계 에멀젼공중합에서 개시제인 ammonium persulfate (APS)의 농도, 보호 콜로이드인 poly(vinyl alcohol) (PVA)의 종류와 농도, 공단량체인 methyl acrylate (MA), ethyl acrylate (EA), n-butyl acrylate (BA)의 혼합비를 변화시켜 중합하였다. 제조된 poly(vinyl acetate-co-methyl acrylate) (PVAc/PMA), poly(vinyl acetate-co-ethyl acrylate) (PVAc/PEA), poly(vinyl acetate-co-n-butyl acrylate) (PVAc/PBA)에 대하여 다음과 같은 결론을 얻었다. 등온 열분해법으로 $100{\sim}200^{\circ}C$ 영역에서 구한 비닐아세테이트와 알킬아크릴레이트 공중합체에 대한 등온 열분해 활성화에너지는 PVAc/PMA > PVAc/PEA > PVAc/PBA이었으며, 플라스마 처리 전과 후의 접착박리강도는 PVAc/PMA > PVAc/PEA > PVAc/PBA의 순이었다.

포도과즙(葡萄果汁) 우유(牛乳) 혼합음료(混合飮料)의 시제(試製) (A Note on Preparation of Acid Milk Drink Containing Natural Grape Juice)

  • 하덕모
    • 한국식품과학회지
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    • 제7권4호
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    • pp.250-253
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    • 1975
  • 포도과즙(果汁), 산유(酸乳), 설탕을 주원료로하여 포도과즙(果汁) 혼합음료를 제조하고 동(同) 음료의 보존성을 검토하여 다음과 같은 결과를 얻었다. 1) 포도과즙(果汁) 산유(酸乳) 혼합음료는 과즙(果汁)중의 colloid와 유(乳)단백질의 결합에 의하여 응집 침전물을 형성하며 가열살균에 의하여 침전물의 형성이 촉진된다. 2) 원료과즙(果汁)의 pectin함량은 제품의 안전성에 직접적으로 관계되며 과즙(果汁)중의 pectin함량은 제품의 안전성에 직접적으로 관계되며 과즙(果汁)중의 pectin함량이 2.5mg% 이하일 때 과즙 $10{\sim}20%$ 혼합시에 있어서도 응집 침전물의 형성을 방지할 수 있다. 3) pectin분해효소로써 처리한 투명과즙(果汁)을 사용하여 제조한 혼합음료는 $85^{\circ}C$ 20분간의 가열살균으로 응집 침전물이 형성되지 않으면 장기간의 저장이 가능하다.

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지시약 적정법 및 분광광도법에 의한 양이온 고분자 전해질의 전해밀도 정량 (Charge Determination of Cationic Polyelectrolytes by Visual Titrimetry and Spectrophotometry)

  • 이민규;김상규
    • 한국환경과학회지
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    • 제14권6호
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    • pp.525-532
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    • 2005
  • Polyelectrolyte titration, which was called colloid titration is based on the stoichiometric reaction between oppositely charged polyelectrolytes, This can be used, for instance, to determine the charge density of a cationic polyelectrolyte, using an anionic polyelectrolyte of known charge density, such as potassium polyvinyl sulfate (PPVS). The technique requires a suitable method of end-point detection and there are several possibilities. In this work, two methods have been investigated: visual titrimetry based on the color change of a cationic dye (o-toluidine blue, o-Tb) and spectrophotometry based on the absorbance change corresponding to the color change of the same dye. These have been applied to several cationic polyelectrolytes with different charge density and molecular weight. In all cases, the cationic charge was due to quaternary nitrogen groups. In the case of cationic dye, it was shown that the sharpness depends on the charge density of cationic polyelectrolyte. With the polyelectrolytes of lower charge density, the binding to PPVS is weaker and binding of the dye to PPVS can occur before all of the polyelectrolyte charge has been neutralized. However, by carrying out titrations at several polyelectrolyte concentrations, good linear relationships were found, from which reliable charge density values could be derived. Effects of pH and ionic strength were also briefly investigated. For cationic polyelectrolytes (copolymers of acrylamide and dimethylaminoethy] acrylate), there was some loss of charge at higher pH values, probably as a result of hydrolysis. Increasing ionic strength causes a less distinct color change of o-Tb, as a result of weaker electrostatic interactions.

콜로이드 계면화학을 이용한 저온형 고체전해질용 $CeO_2$계 복합 산화물의 소결체 제조 (The Preparation for Sintered Body of $CeO_2$ Based Complex Oxide in Low Temperature Solid Oxide Fuel Cells Using Colloidal Surface Chemistry)

  • 황용신;최성철
    • 한국세라믹학회지
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    • 제37권7호
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    • pp.705-712
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    • 2000
  • In this study, the dispersion stability of CeO2 based complex oxide was studied, and density, porosity, and microstructure of green body were investigated using colloid surface chemistry to manufacture the Gd2O3 doped CeO2 solid electrolyte in an aqueous system. To prepare the stable slurry for slip casting, the dispersion stability was examined as a function of pH using ESA(electrokinetic sonic anplitude) analysis. The dynamic mobility of particles was enhanced with anionic and cationic dispersant were added the amount of 0.5wt% respectively, but pH value in slurries didn't move to below 6.0 because of the influence of dopants. This phenomenon also appeared in the CeO2-Y2O3 and CeO2-Sm2O3 systems, so it could be inferred that rare earth dopants such as Gd2O3, Sm2O3 and Y2O3 not only have the similar motion with changing pH in an aqueous system but also can be dissolved in the range of pH 6.0∼6.5. In CeO2-Gd2O3 system, when the anionic dispersant was added the amount of 0.5wt% and pH value in slurries was fixed at 9.5, the green body density was 4.07g/㎤, and the relative density of sintered body was 95.2%. It could be inferred from XRD analysis that Gd3+ substituted into Ce4+ site because there was no free Gd2O3 peak.

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ZnO와 TiO2 함유 복합나노섬유의 제조와 유해물질분해 성능 평가 (Fabrication of ZnO and TiO2 Nanocomposite Fibers and Their Photocatalytic Decomposition of Harmful Gases)

  • 허윤선;이승신
    • 한국의류학회지
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    • 제35권11호
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    • pp.1297-1308
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    • 2011
  • This research investigates the application of ZnO (zinc oxide) nanoparticles and $TiO_2$ (titanium dioxide) nanoparticles to polypropylene nonwoven fabrics via an electrospinning technique for the development of textile materials that can decompose harmful gases. To fabricate uniform ZnO nanocomposite fibers, two types of ZnO nanoparticles were applied. Colloidal $TiO_2$ nanoparticles were chosen to fabricate $TiO_2$ nano- composite fibers. ZnO/poly(vinyl alcohol) (PVA) and $TiO_2$/PVA nanocomposite fibers were electrospun under a variety of conditions that include various feed rates, electric voltages, and capillary diameters. The morphology of electrospun nanocomposite fibers was examined with a field-emission scanning electron micro- scope and a transmission electron microscope. Decomposition efficiency of gaseous materials (formaldehyde, ammonia, toluene, benzene, nitrogen dioxide, sulfur dioxide) by nanocomposite fiber webs with 3wt% nano-particles (ZnO or $TiO_2$) and 7$g/m^2$ web area density was assessed. This study shows that ZnO nanoparticles in colloid were more suitable for fabricating nanocomposite fibers in which nanoparticles are evenly dispersed than in powder. A heat treatment was applied to water-soluble PVA nanofiber webs in order to stabilize the electrospun nanocomposite fibrous structure against dissolution in water. ZnO/PVA and $TiO_2$/PVA nanofiber webs exhibited a range of degradation efficiency for different types of gases. For nitrogen dioxide, the degradation efficiency was 92.2% for ZnO nanocomposite fiber web and 87% for $TiO_2$ nanocomposite fiber web after 20 hours of UV light irradiation. The results indicate that ZnO/PVA and $TiO_2$/PVA nano- composite fiber webs have possible uses in functional textiles that can decompose harmful gases.

Au/TiO2 core-shell 나노입자의 합성에 있어서 Au 나노입자의 분산특성에 미치는 Mercaptoundecanoic acid (MUA)의 피복 효과 (The Effect of Mercaptoundecanoic Acid (MUA) Coating on Dispersion Property of Au Nanoparticles in Synthesis of Au/TiO2 Core-shell Nanoparticles)

  • 유연태;김병규
    • 한국재료학회지
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    • 제16권12호
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    • pp.754-760
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    • 2006
  • Mercaptoundecanoic acid (MUA) has been used to enhance the dispersity of Au nanoparticles in organic solvent and the affinity between the Au nanoparticles surface and titanium dioxide shell in the synthesis of $Au/TiO_2$ core-shell composite nanoparticles. The dispersity of the MUA-coated Au nanoparticles in ethanol aqueous solution with different concentration of $H_2O$ was investigated by UV-Vis. absorption spectrum and the coating amount of MUA was varied from 0.02 mM to 1.0 mM. The MUA-coated Au nanoparticles were highly dispersed in pure $H_2O$ in the wide range of the coating amount of MUA. On the contrary, the MUAcoated Au nanoparticles showed an enhanced stability in the ethanol/$H_2O$=8/2 mixed solution only when the coating amount of MUA was 0.05 mM, and in the ethanol/$H_2O$=7/3 mixed solution when the coating amount of MUA was in the range from 0.02 mM to 0.17 mM. From this systematic study, it can be inferred that the stability and the dispersibility of Au nanoparticles in organic solvents are highly sensitive towards the amount of MUA coating.

하이퍼써미아 응용을 위한 하이브리드 에어로젤 내 분산된 마그네타이트 나노입자 (Magnetite Nanoparticles Dispersed in Hybrid Aerogel for Hyperthermia Application)

  • 이은희;좌용호;김창열
    • 한국재료학회지
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    • 제22권7호
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    • pp.362-367
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    • 2012
  • Magnetite nanoparticles(NPs) have been the subject of much interest by researchers owing to their potential use as magnetic carriers in drug targeting and as a tumor treatment in cases of hyperthermia. However, magnetite nanoparticles with 10 nm in diameter easily aggregate and thus create large secondary particles. To disperse magnetite nanoparticles, this study proposes the infiltration of magnetite nanoparticles into hybrid silica aerogels. The feasible dispersion of magnetite is necessary to target tumor cells and to treat hyperthermia. Magnetite NPs have been synthesized by coprecipitation, hydrothermal and thermal decomposition methods. In particular, monodisperse magnetite NPs are known to be produced by the thermal decomposition of iron oleate. In this study, we thermally decomposed iron acetylacetonate in the presence of oleic acid, oleylamine and 1,2 hexadecanediol. We also attempted to disperse magnetite NPs within a mesoporous aerogels. Methyltriethoxysilicate(MTEOS)-based hybrid silica aerogels were synthesized by a supercritical drying method. To incorporate the magnetite nanoparticles into the hybrid aerogels, we devised two methods: adding the synthesized aerogel into a magnetite precursor solution followed by nucleation and crystal growth within the pores of the aerogels, and the infiltration of magnetite nanoparticles synthesized beforehand into aerogel matrices by immersing the aerogels in a magnetite nanoparticle colloid solution. An analysis using a vibrating sample magnetometer showed that approximately 20% of the magnetite nanoparticles were well dispersed in the aerogels. The composite samples showed that heating under an inductive magnetic field to a temperature of $45^{\circ}C$ is possible.

간(肝)스캔상(上) 체위변동(體位變動)에 따른 간형태(肝形態) 변화(變化)에 대(對)한 고찰(考察) (A Study on the Effects of Position Change on the Liver Shape on Radioisotope Scan)

  • 홍기석;최두혁;양영태;고창순
    • 대한핵의학회지
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    • 제16권1호
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    • pp.49-54
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    • 1982
  • For this study, the authors obtained and examined anterior views of the liver and spleen in two different positions, upright and supine, of 39 normal subjects and 20 patients with hepaticpathology by means of $^{99m}Tc-colloid$ and gamma camera. This examination confirms the following findings. In general, it is shown, left lobe of the liver in upright position becomes longer in height than in supine position, while the distance between lateral margin of the liver and that of the spleen becomes father in with in supine position than in upright position. The upper margin of liver moves more downward in upright position than in supine. It is noticeable that as for 5 cases with severe chronic liver disease, there is minimal alteration of the liver shape between in two positions. The comparison of the both positions for the better liver scan shows the following finding. Prominent caudate and/or left lobe are marked in the upright position in 16 cases out of the total 59, while none is found in the supine. The false cold area in lower part of the liver disappears in 7 cases in the upright position, while only one shows the disappeance of the false cold area in the supine. Left liver margin due to close contact of spleen is blurred in 3 cases in the upright position. In total 23 cases out of 59 support that the upright position is better for the liver scan, while only 4 cases support the supine position is better. These findings support two assumptions. One is that upright view can bo expected more improved resoluton than supine view for liver scan. Second is that minimal change of the liver shape in both views indicate the serious abnormality in the liver.

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