• Title/Summary/Keyword: Mg particles

검색결과 738건 처리시간 0.034초

Lead-free inorganic metal perovskites beyond photovoltaics: Photon, charged particles and neutron shielding applications

  • Srilakshmi Prabhu;Dhanya Y. Bharadwaj;S.G. Bubbly;S.B. Gudennavar
    • Nuclear Engineering and Technology
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    • 제55권3호
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    • pp.1061-1070
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    • 2023
  • Over the last few years, lead-free inorganic metal perovskites have gained impressive ground in empowering satellites in space exploration owing to their material stability and performance evolution under extreme space environments. The present work has examined the versatility of eight such perovskites as space radiation shielding materials by computing their photon, charged particles and neutron interaction parameters. Photon interaction parameters were calculated for a wide energy range using PAGEX software. The ranges of heavy charged particles (H, He, C, N, O, Ne, Mg, Si and Fe ions) in these perovskites were estimated using SRIM software in the energy range 1 keV-10 GeV, and that of electrons was computed using ESTAR NIST software in the energy range 0.01 MeV-1 GeV. Further, the macroscopic fast neutron removal cross-sections were also calculated to estimate the neutron shielding efficiencies. The examined shielding parameters of the perovskites varied depending on the radiation type and energy. Among the selected perovskites, Cs2TiI6 and Ba2AgIO6 displayed superior photon attenuation properties. A 3.5 cm thick Ba2AgIO6-based shield could reduce the incident radiation intensity to half its initial value, a thickness even lesser than that of Pb-glass. Besides, CsSnBr3 and La0.8Ca0.2Ni0.5Ti0.5O3 displayed the highest and lowest range values, respectively, for all heavy charged particles. Ba2AgIO6 showed electron stopping power (on par with Kovar) better than that of other examined materials. Interestingly, La0.8Ca0.2Ni0.5Ti0.5O3 demonstrated neutron removal cross-section values greater than that of standard neutron shielding materials - aluminium and polyethylene. On the whole, the present study not only demonstrates the employment prospects of eco-friendly perovskites for shielding space radiations but also suggests future prospects for research in this direction.

적조생물의 구제 -1. IOSP에 의한 적조생물의 응집제거- (Removal of Red Tide Organisms -1. flocculation of Red Tide Organisms by Using IOSP-)

  • 김성재;조규대
    • 한국수산과학회지
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    • 제33권5호
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    • pp.448-454
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    • 2000
  • IOSP를 이용하여 적조생물입자에 대한 응집실험을 한 결과는 다음과 같다. 본 실험에 사용한 IOSP의 평균 지름은 $11.6{\mu}m$이고, 약$ 77{\%}$의 입자가 $5.0{\~}20.0{\mu}$의 범위에 속하며 변동계수는 $60.1{\%}$이었다. IOSP의 금속성분을 분석한 결과는 $98{\%}$가 칼슘으로서 생석회(CaO)와 같은 성분이었다. IOSP의 전자현미경 사진을 분석한 결과 표면이 매끈한 부정형의 입자로 되어 있었다. IOSP에 해수를 첨가하면 해수중의 $Mg^(+2)$ 이온과 급속하게 반응하여 입자의 표면 주위에 점질성의 $Mg(OH)_2$ 흡수층 (absorption layer)을 형성하여 응집 침전하고 해수의 pH를 10.0 정도까지 상승시켰다. IOSP는 $pH=6.2{\~}12.7$에서 $11.1{\~}50.1 mV$로서 IOSP의 입자가 완전히 용해될 때까지 positive zeta potential을 나타낸 반면 OSP는 pH=9.2, 11.9에서 각각 -42.5, -56.9mV로서 negative zeta potential을 나타내었다. $pNa=2.0{\~}4.0 (10^(-4){\~}10^(-2)M Na^+)$에서 IOSP, OSP의 zeta potential은 거의 일정한 값을 나타내었으나 $pNa=0.0 (1 M Na^+)$에서는 IOSP의 EDL이 매우 크게 압축되어 zeta potential은 거의 0.0mV를 나타내었고 OSP는 -25.4mV의 여전히 높은 negative zeta potential을 나타내었다. IOSP는 $Mg^(+2)$ 이온의 농도가 증가함에 따라 positive zeta potential이 증가하다가 $pMg=3.0 (10^(-3)M Mg^(+2))$에서 감소하는 결과를 나타내었다. 해수 중에서 IOSP는 4.8mV의 positive zeta potential을 나타내었고, OSP와 RTO는 각각 -30.7mV, -9.2mV의 negative zeta potential을 나타내었다. 해수중에서 IOSP의 $Mg(OH)_2$ 흡수층과 적조생물입자 사이에는 positive-negative EDL 반응이 일어나서 이들 둘 사이에는 항상 전기동력학적 인력이 작용하고, 동시에 $Mg(OH)_2$ 흡수층에 의한 전하중화로 인하여 입자 상호간의 응집반응은 극단적 인력이 작용하는 primary minimum에서 일어나고, DLVO 이론에 따라 응집반응은 비가역적아며 매우 신속하게 일어났다. 적조생물입자의 응집제거 효율은 IOSP의 농도 50mg/l까지 급격한 증가를 보이다가 IOSP의 농도가 계속 증가함에 따라서 점점 완만한 증가를 나타내었다. 즉 IOSP의 농도가 증가함에 따라서 지수함수적으로 증가하였다 ($Y=53.81{\times}X^(0.1); R^2=0.9868$).응집 침전은 IOSP 400mg/l 이상에서 거의 완전히 일어났다. IOSP $100mg/l$을 사용하고 G-value를 $1, 6, 29, 139 sec^(-1)$로 단계적으로 증가시키면서 응집 실험을 한 결과 적조생물입자의 응집제거 효율이 각각 $70.5, 70.5, 81.7, 85.3{\%}$로 증가하였다. 이는 응집 반응에서 입자간 충분한 충돌이 일어날 수 있도록 교반하는 것이 매우 중요함을 나타내 주는 것이다.

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해양차량 경량화용 마그네슘합금의 마찰용접 및 AE 특성 (Friction Welding and AE Characteristics of Magnesium Alloy for Lightweight Ocean Vehicle)

  • 공유식;이진경;강대민
    • 한국해양공학회지
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    • 제25권6호
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    • pp.91-96
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    • 2011
  • In this paper, friction welded joints were constructed to investigate the mechanical properties of welded 15-mm diameter solid bars of Mg alloy (AZ31B). The main friction welding parameters were selected to endure reliable quality welds on the basis of visual examination, tensile tests, impact energy test, Vickers hardness surveys of the bonds in the area and heat affected zone (HAZ), and macrostructure investigations. The study reached the following conclusions. The tensile strength of the friction welded materials (271 MPa) was increased to about 100% of the AZ31B base metal (274 MPa) under the condition of a heating time of 1 s. The metal loss increased lineally with an increase in the heating time. The following optimal friction welding conditions were determined: rotating speed (n) = 2000 rpm, heating pressure (HP) = 35 MPa, upsetting pressure (UP) = 70 MPa, heating time (HT) = 1 s, and upsetting time (UT) = 5 s, for a metal loss (Mo) of 10.2 mm. The hardness distribution of the base metal (BM) showed HV55. All of the BM parts showed levels of hardness that were approximately similar to friction welded materials. The weld interface of the friction welded parts was strongly mixed, which showed a well-combined structure of macro-particles without particle growth or any defects. In addition, an acoustic emission (AE) technique was applied to derive the optimum condition for friction welding the Mg alloy nondestructively. The AE count and energy parameters were useful for evaluating the relationship between the tensile strength and AE parameters based on the friction welding conditions.

남양호 퇴적물에서 영양염류 용출 특성 분석 (Sediment Release Rate of Nutrients from Namyang Reservoir)

  • 조영철;정세웅
    • 대한환경공학회지
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    • 제29권12호
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    • pp.1345-1352
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    • 2007
  • 퇴적물로부터 용출되는 영양염류가 인공호수인 남양호의 수질에 미치는 영향을 예측하기 위하여, 실험실에서 퇴적물의 조건을 호기 및 혐기조건으로 설정한 후 영양염류의 용출속도를 측정하였다. 퇴적물로부터 유기물과 질소의 용출은 일어나지 않는 것으로 판단된다. 인산염 인과 총인의 경우 수체 내 산소조건에 따라 용출 양상이 달랐는데, 혐기조건에서는 인이 용출되지 않은 반면, 호기 조건에서는 많은 양의 인이 용출되었다. 실험 결과를 기초로 호기조건에서 인의 용출 속도를 계산한 결과 인산염 인의 경우 $1.01\sim2.48$ mg-P/$m^2$/day이며, 총인의 경우는 $2.14\sim3.54$ mg-P/$m^2$/day로 나타났다. 상류에서 채집한 퇴적물에서 인의 용출 속도가 가장 빨랐는데, 이는 유입수에 쉽게 분해 가능한 유기물이 다량 포함되어 있기 때문으로 사료된다. 남양호의 경우 가장 깊은 하류의 수심이 $7\sim14$ m로 성층화가 이루어지지 않기 때문에, 대부분의 퇴적물 환경이 호기성 상태이다. 본 연구의 결과 남양호 퇴적물 중에 포함된 인이 호기성 상태에서 다량 용출되고 있기 때문에 인의 용출에 의한 수질 오염 문제에 대한 적절한 대책이 필요할 것으로 판단된다.

은행나무 잎을 혼합하여 제조한 파티클보드의 물리.기계적 성질과 포름알데히드 저감효과 (Physico-Mechanical Properties and Formaldehyde Abatement of Particleboard Mixed with Gingko Tree Leaves)

  • 박상범
    • 임산에너지
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    • 제25권2호
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    • pp.28-33
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    • 2006
  • 본 연구에서는 대기오염에 대한 저항성과 내충성, 항균성 등이 강하여 가로수로 많이 심어진 은행나무에 있어서, 그 잎의 파티클보드 제조 원료로서의 가능성을 모색하고자 하였다. 이를 위해 은행나무 잎을 분쇄한 다음 목재 파티클에 소량 혼합하여 파티클보드를 제조하였다. 은행나무 잎을 혼합하여 제조한 파티클보드의 물리, 기계적 성질을 조사하고 포름알데히드 방출량의 저감효과에 대해 검토하였다. 목재 파티클에 대하여 은행나무 잎을 $1{\sim}5%$ 첨가하여 제조한 파티클보드는 은행나무 잎을 첨가하지 않은 대조구에 비해 밀도, 함수율, 흡수두께팽창률 등 물리적 성질과 휨강도, 박리강도와 같은 기계적 성질은 크게 감소하지 않았으며 모두 KS 파티클보드의 기준을 만족하였다. 은행나무 잎의 혼합량에 따라 포름알데히드 방출량은 점차 감소하였으며, 특히 은행나무 잎이 3% 첨가된 파티클보드의 포름알데히드 방출량은 $2.81mg/{\ell}$에서 $1.66mg/{\ell}$로 대조구에 비해 약 40% 감소하였다. 은행나무 잎이 지닌 고유한 항균성에 덧붙여 본 연구로부터 얻어진 결과는 낙엽으로 폐기되는 은행나무 잎을 원료로 포름알데히드 방출량이 낮은 기능성 파티클보드를 제조할 수 있다는 새로운 사실을 보여주고 있다.

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$TiO_2$ 광촉매를 처리한 Diazinon의 광분해에 관한 연구 (The study for photodegradation of diazinon using $TiO_2$ photocatalyst)

  • 류성필;오윤근
    • 한국환경과학회지
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    • 제9권2호
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    • pp.151-158
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    • 2000
  • Considerable interest has been shown in recent years towards utilizing $TiO_2$ particles as a photocatalyst in the degradation of harmful organic contaminants. In this study, photocatalytic degradation of diazinon which is extensively used as a pesticide in the agriculture field, has been investigated with UV-illuminated $TiO_2$ weight, UV wavelength, pH of the solution. Photodegradation rate increased with decreasing initial concentration of diazinon and with increasing pH of the solution. Photodegradation rate increased with increasing $TiO_2$ weight, but was nearly the same at $TiO_2$ weight of 1g/$\ell$, 2 g/$\ell$, i.e., for initial diazinon concentratin of 5 mg/$\ell$. UV wavelength affecting on the degradation rate of diazinon decreased in the order of 254 nm>312 nm> 365 nm. For $TiO_2$ weight of 1 g/$\ell$and initial diazinon concentration of 5 mg/$\ell$, the photodegradation removal of diazinon was 100% after 130 min in the case of 254 nm, but 95% in the case of 312 nm, and 84% in the case of 365nm, after 180 min. The photodegradation of diazinon followed a first order or a pseudo - first order reaction rate. For initial diazinon concentration of 5 mg/$\ell$, the rate constants(k) in UV and $TiO_2$(1 g/$\ell$)/UV system were $0.006 min^{-1} and 0.0252 min^{-1} at 254 nm, 0.0055 min^{-1} and 0.0104 min^{-1} at 312 nm, and 0.004 min^{-1}$ at 365 nm respectively.

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Adsorption of methylene blue from an aqueous dyeing solution by use of santa barbara amorphous-15 nanostructure: Kinetic and isotherm studies

  • Alizadeh, Reza;Zeidi, Amir
    • Advances in environmental research
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    • 제6권2호
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    • pp.113-125
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    • 2017
  • Santa Barbara Amorphous-15(SBA-15) nanoparticles were utilized as the inexpensive and effective adsorbents to remove methylene blue dye from the aqueous solution.SBA-15 was created by Zhao et al method. Infrared spectroscopy, X-ray diffraction and scanning electron microscopy (SEM) were used for the evaluated physical properties of SBA-15. The results of diffraction X-ray indicated that was the crystalline structure for it. Also IR spectroscopy indicated was a silica the whole structure of the groups and SEM image verify the structure of relatively identical particles size of SBA-15. Factors affecting adsorption including the amounts of adsorbent, pH and contact time were investigated by a SBA-15 nanomaterial design. The extent of dye removal enhanced with increasing initial dye concentration and pH from 4 to 10. The higher percentage adsorption were obtained under optimum conditions of variables (sorbent dose of 200 mg/liter, initial MB concentration 10 mg/liter, initial pH of 10 and temperature of $25^{\circ}C$). Maximum adsorption happened after the 2 hour and the kinetic processes of the dyes adsorption were described by applying the pseudo-first-order and the pseudo-second-order and the relatively High correlation with the kinetic Ellovich models. It was found that the pseudo-second-order models kinetic equation described the data of dye adsorption with a good correlation (R2>0.999) which indicated chemisorption mechanism. Freundlich and Langmuir adsorption models were investigated in conditions of variables (adsorbent dose 0.01 gr/liter, MB concentration 10, 20, 30 mg/liter, pH of 4, 7, 10, contact time 90 min and temperature of $27^{\circ}C$). The adsorption data were represented by Langmuir isotherm model. These values are higher than the adsorption capacities of some other adsorbents that have recently been published in the literature.

$Bi_2O_3{\cdot}3TiO_2$의 첨가량에 따른 $(SrPb)(CaMg)TiO_3$ 세라믹의 전기적 특성 (The Electrical Properties of $(SrPb)(CaMg)TiO_3$ Ceramics with Contents of $Bi_2O_3{\cdot}3TiO_2$)

  • 김충혁
    • 한국전기전자재료학회논문지
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    • 제11권2호
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    • pp.111-120
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    • 1998
  • In this paper, the $(SrPb)(CaMg)TiO_3$ ceramics with paraelectric properties were fabricated by the mixed oxide method. It was investigated that which the variation of contents of $Bi_2O_3{\cdot}3TiO_2$ effects on structural, dielectrical and electrical properties of specimens. As a result, the grain size were grown with increasing the contents of $Bi_2O_3{\cdot}3TiO_2$. The relative dielectric constants were increased up to 4[mol%] of $Bi_2O_3{\cdot}3TiO_2$, and decreased more or less at a low temperature in the specimens which had more than. But the temperature coefficient. of capacitance were showed ${\pm}25$[%]. The dielectric loss were less than 0.05 in all specimens which had more than 4[mol%] of $Bi_2O_3{\cdot}3TiO_2$. In order to investigate the behavior of charged particles, the characteristics of electrical conduction were measured. As a result, the conduction current was divided into the three steps as a function of DC electric field. The first step was Ohmic region due to ionic conduction, below 15[kV/cm]. The second step was showed a saturation which seems to be related to a depolarizing field occuring in field-enforced ferroelectric phase, between 15[kV/cm] and 40[kV/cm]. The third step was attributed to Child's law related to space charge which injected from electrode, above 40[kV/cm].

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Preparation and Analysis of Yeast Cell Wall Mannoproteins, Immune Enhancing Materials, from Cell Wall Mutant Saccharomyces cerevisiae

  • Ha Chang-Hoon;Yun Cheol-Won;Paik Hyun-Dong;Kim Seung-Wook;Kang Chang-Won;Hwang Han-Joon;Chang Hyo-Ihl
    • Journal of Microbiology and Biotechnology
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    • 제16권2호
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    • pp.247-255
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    • 2006
  • Yeast cell wall matrix particles are composed entirely of mannoprotein and ${\beta}-glucan$. The mannoproteins of yeast cell wall can systemically enhance the immune system. We previously purified and analyzed alkali-soluble ${\beta}-glucans$ [${\beta}$-(1,3)- and ${\beta}$-(1,6)-glucans] [10]. In the present study, a wild-type strain was first mutagenized with ultraviolet light, and the cell wall mutants were then selected by treatment with 1.0 mg/ml laminarinase (endo-${\beta}$-(1,3)-D-glucanase). Mannoproteins of Saccharomyces cerevisiae were released by laminarinase, purified by concanavalin-A affinity and ion-exchange chromatography. The results indicated that the mutants yielded 3-fold more mannoprotein than the wild-type. The mannoprotein mass of mutant K48L3 was 2.25 mg/100 mg of yeast cell dry mass. Carbohydrate analysis revealed that they contained mannose, glucose, and N-acetylglucosamine. Saccharomyces cerevisiae cell wall components, mannoproteins, are known to interact with macrophages through receptors, thereby inducing release of tumor necrosis factor alpha ($TNF-{\alpha}$) and nitric oxide. Mannoprotein tractions in the present study had a higher macrophage activity of secretion of $TNF-{\alpha}$ and nitric oxide and direct phagocytosis than positive control ($1{\mu}g$ of lipopolysaccharide). In particular, F1 and F3 fractions in mannoproteins of K48L3 enhanced and upregulated the activity of nitric oxide secretion and macrophage phagocytosis by approximately two- and four-fold, respectively.

충남대학교 대덕캠퍼스내 상수도 물의 수리지구화학적 특성 (Hydrogeochemistry of Supply Water in the Daedeok Campus of Chungnam National University, Korea)

  • 이찬희
    • 자원환경지질
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    • 제33권3호
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    • pp.181-193
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    • 2000
  • This study was undertaken to evaluate the drinking water quality based on physicochemical properties and chemical compositions of the supply water in the Daedeok Campus, and to verify the analytical reliabilities of ICP-MS and IC equipped in the Central Research Facilities at Chungnam National University , Korea. The supply water belongs to $Ca^{2+}-({HCO_3}^-+{SO_4}^{2-})$type, whereas the original water from the Daecheong lake belongs to $(Ca^{2+}-(Mg^{2+})-{HCO_3}^-$ type. Generally, temperature (14.1$^{\circ}C$), pH (6.95), Eh (0 mV), electrical conductivity (117${\mu}$S/cm) and TDS (86.975mg/l) of supply water were higher than those of original lake water . Results using WATEQ4F revealed that potentially toxic ions of the supply water might exist mainly as free metals ($M^{2+}$) and a small amount as ${CO_3}^{2-}$ and $OH^-$ complexes. Also, the water composition belongs to the kaolinite field. Calculated average enrichment indies of the supply water normalized to lake water for anions, mamor cations, toxic cations and total ions are 1.05 , 1.56, 13.05 and 1.17 , respectively. Those values of the ground water in the Daedeok Campus showed 1.71, 4.78, 5.71 and 2.49 , respectively. However , contents of all constituents of these water are within the drinking water standard. All samples were filtered before the chemical analysis. Pale yellow or yellowish brown colored materials of colloidal particles coated the filter paper to thickness of 0.02 to 0.2mm. these are mainly Fe-Cy-Zn compounds with traces of Ni and Pb, the net weights of which compounds range from 0.01to 3.20mg/l. Most elements did not show any conceivable filtering effect of Cu, Fe and Zn. Especially, mean concentration of total Fe decreased considerably from 168.52${\mu}g$/lto 42.58${\mu}g$/l by filtering .

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