• Title/Summary/Keyword: ion composition

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Competition between ICME and crustal magnetic field on the loss of Mars atmosphere

  • Hwang, Junga;Jo, Gyeongbok;Kim, Roksoon;Jang, Soojeong;Cho, Kyungsuk;Lee, Jaejin;Yi, Yu
    • The Bulletin of The Korean Astronomical Society
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    • v.42 no.2
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    • pp.62.3-63
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    • 2017
  • The Mars Atmosphere and Volatile (MAVEN) mission has been providing valuable information on the atmospheric loss of Mars since its launch in November 2013. The Neutral Gass and Ion Mass Spectrometer (NGIMS) onboard MAVEN, was developed to analyze the composition of the Martian upper atmospheric neutrals and ions depending on various space weather conditions. We investigate a variation of upper atmospheric ion densities depending on the interplanetary coronal mass ejections (ICMEs). It is known that the Mars has a very weak global magnetic field, so upper atmosphere of Mars has been strongly affected by the solar activities. Meanwhile, a strong crustal magnetic field exists on local surfaces, so they also have a compensating effect on the upper atmospheric loss outside the Mars. The weak crustal field has an influence up to 200km altitude, but on a strong field region, especially east longitude of $180^{\circ}$ and latitude of $-50^{\circ}$, they have an influence over 1,400km altitude. In this paper, we investigated which is more dominant between the crustal field effect and the ICME effect to the atmospheric loss. At 400km altitude, the ion density over the strong crustal field region did not show a significant variation despite of ICME event. However, over the other areas, the variation associated with ICME event is far more overwhelming.

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Study of PSII-treated PMMA, PHEMA, and PHPMA ; Investigation of Their Surface Stabilities

  • Hyuneui Lim;Lee, Yeonhee;Seunghee Han;Jeonghee Cho;Moojin suh;Kem, Kang-Jin
    • Proceedings of the Korean Vacuum Society Conference
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    • 1999.07a
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    • pp.204-204
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    • 1999
  • The plasma source ion implantation(PSII) technique which is a method using high negative voltage pulse in plasma system has the potential to change the surface properties of polymer. PSII technique increase the surface free energy by introducing polar functional groups on the surface so that it improves reactivity, hydrophilicity, adhension, biocompatability, etc. However, the mobility of polymer chains enables the modified surface layers to adapt their composition to interfacial force. This hydrophobic recovery interrupts the stability of modified surfaces to keep for the long time. In this study, poly(methyl methacrylate)(PMMA), poly(2-hydroxyethyl methacrylate)(PHEMA), and polu(2-hydroxypropyl methacylate)(PHPMA) for contact lens application, were modified to improve the wettability with PSII technique and were investigated the surface stabilities. Polymer film was prepared with solution casting(3 wt.% solution) and was annealed at 11$0^{\circ}C$ under vacuum oven to remove solvent completely and to eliminate physical ageing. The thickness of the film measured by scanning electron microscopy (SEM) and surface profilometer was about 10${\mu}{\textrm}{m}$. Polymers were treated with different kinds of gases, pulse frequency, pulse with, pulse voltage, and treatment time. Even though PMMA, PHEMA, and PHPMA have similar repeat unit structure, the optimal treatment conditions and the tendency to hydrophobic recovery were different. PHPMA, more hydrophilic polymer than PMMA and PHEMA showd better wettability and stability after mild treatment. Surface tensions were obtained by water and diiodomethane contact angle measurements to monitor the relation between hydrophobic recovery and polymer structure. Different ion species in plasma change the polar component and dispersion component of polymer surface. For better wettability surface, the increase of polar component was a dominant factor. We also characterized modified polymer surfaces using x-ray photoelectron spectroscopy(XPS), secondary ion mass spectrometry(SIMS), Fourier Transform infrared spectroscopy(FT-IR), and SEM.

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Reactive ion etching of InP using $Cl_2/CH_4/H_2$ discharges ($Cl_2/CH_4/H_2$ 혼합기체를 이용한 InP 소재의 반응성 이온 에칭에 관한 연구)

  • 최익수;이병택;김동근;박종삼
    • Journal of the Korean Vacuum Society
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    • v.6 no.3
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    • pp.282-286
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    • 1997
  • Reactive ion etching (RIE) characteristics of InP in the $Cl_2$/ CH_4/H_2$ discharges was investigated, as a function of the rf power, substrate temperature and gas composition. It was observed that the etch rate increased as the rf power, sample temperature and/or $Cl_2$ gas concentration increased. Etch rate of about 0.9$\mu\textrm{m}$/min was obtained at the optimum condition of 150W rf power, $180^{\circ}C$ substrate temperature and $10Cl_2$ /$5CH_4/85H_2$ gas ratio. Polymer formation was completely suppressed by adding $Cl_2$ to the $CH_4$ /$H_2$ discharges.

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Properties and Functions of Melanin Pigment from Klebsiella sp. GSK

  • Sajjan, Shrishailnath S.;Anjaneya, O;Kulkarni, Guruprasad B.;Nayak, Anand S.;Mashetty, Suresh B.;Karegoudar, T.B.
    • Microbiology and Biotechnology Letters
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    • v.41 no.1
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    • pp.60-69
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    • 2013
  • Purified melanin pigment from Klebsiella sp. GSK was characterized by thermogravimetric, differential thermal, X-ray diffraction and elemental analysis. This melanin pigment is structurally amorphous in nature. It is thermally stable up to $300^{\circ}C$ and emits a strong exothermic peak at $700^{\circ}C$. Its carbon, hydrogen and nitrogen composition is 47.9%, 6.9% and 12.0%, respectively. It was used to scavenge metal ions and free radicals. After immobilizing the pigment and using it to adsorb copper and lead ions, the metal ion adsorption capacity was evaluated by atomic absorption spectroscopy (AAS) and the identity of melanin functional groups involved in the binding of metal ions was determined by Fourier transform infrared (FT-IR) spectroscopy. Batch adsorption studies showed that 169 mg/g of copper and 280 mg/g of lead were adsorbed onto melanin-alginate beads. The metal ion adsorption capacity of the melanin-alginate beads was relatively significant compared to alginate beads. The metal ion desorption capacity of HCl was greater (81.5% and 99% for copper and lead, respectively) than that of EDTA (80% and 71% for copper and lead, respectively). The ability of the melanin pigment to scavenge free radicals was evaluated by inhibition of the oxidation of 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) and was shown to be about 74% and 98%, respectively, compared with standard antioxidants.

Decision of Interface and Depth Scale Calibration of Multilayer Films by SIMS Depth Profiling

  • Hwang, Hye-Hyun;Jang, Jong-Shik;Kang, Hee-Jae;Kim, Kyung-Joong
    • Proceedings of the Korean Vacuum Society Conference
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    • 2012.02a
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    • pp.274-274
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    • 2012
  • In-depth analysis by secondary ion mass spectrometry (SIMS) is very important for the development of electronic devices using multilayered structures, because the quantity and depth distribution of some elements are critical for the electronic properties. Correct determination of the interface locations is critical for the calibration of the depth scale in SIMS depth profiling analysis of multilayer films. However, the interface locations are distorted from real ones by the several effects due to sputtering with energetic ions. In this study, the determination of interface locations in SIMS depth profiling of multilayer films was investigated by Si/Ge and Ti/Si multilayer systems. The original SIMS depth profiles were converted into compositional depth profiles by the relative sensitivity factors (RSF) derived from the atomic compositions of Si-Ge and Si-Ti alloy reference films determined by Rutherford backscattering spectroscopy. The thicknesses of the Si/Ge and Ti/Si multilayer films measured by SIMS depth profiling with various impact energy ion beam were compared with those measured by TEM. There are two methods to determine the interface locations. The one is the feasibility of 50 atomic % definition in SIMS composition depth profiling. And another one is using a distribution of SiGe and SiTi dimer ions. This study showed that the layer thicknesses measured with low energy oxygen and Cs ion beam and, by extension, with method of 50 atomic % definition were well correlated with the real thicknesses determined by TEM.

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MWCNT, silver nanoparticles, CuBTC를 사용한 염소 이온 센서 합성

  • Gwak, Byeong-Gwan;Park, Su-Bin;Yu, Bong-Yeong
    • Proceedings of the Korean Institute of Surface Engineering Conference
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    • 2018.06a
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    • pp.101-101
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    • 2018
  • Quantitative measurement of chloride ion concentration has an important role in various fields of electrochemistry, medical science, biology, metallurgy, architecture, etc. Among them, its importance of architecture is ever-growing due to unexpected degradations of building structure. These situations are caused by corrosion of reinforced concrete (RC) structure of buildings. And chloride ions are the most powerful factors of RC structure corrosion. Therefore, precise inspection of chloride ion concentration must be required to increase the accuracy of durability monitoring. Multi-walled Carbon nanotubes (MWCNTs) have high chemical resistivity, large surface area and superior electrical property. Thus, it is suitable for the channels of electrical signals made by the sensor. Silver nanoparticles were added to giving the sensing property. CuBTC, one of the metal organic frameworks (MOFs), was employed as a material to improve the sensing property because of its hydrophilicity and high surface area to volume ratio. In this study, sensing element was synthesized by various chemical reaction procedures. At first, MWCNTs were functionalized with a mixture of sulfuric acid and nitric acid because of enhancement of solubility in solution and surface activation. And functionalized MWCNTs, silver nanoparticles, and CuBTC were synthesized on PTFE membrane, one by one. Electroless deposition process was performed to deposit the silver nanoparticles. CuBTC was produced by room temperature synthesis. Surface morphology and composition analysis were characterized by scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), respectively. X-ray photoelectron spectroscopy (XPS) was also performed to confirm the existence of sensing materials. The electrical properties of sensor were measured by semiconductor analyzer. The chloride ion sensing characteristics were confirmed with the variation of the resistance at 1 V.

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A Study on the friction and Wear Characteristics of C-N Coated SCM415 Steel (C-N코팅 SCM415강의 마찰$\cdot$마모 특성에 관한 연구)

  • Lyu Sung-ki;Lu Long;Jin Tai-yu;Lian Zhe-Man;Cao Xing-Jin;Cho Sung-Min
    • Journal of the Korean Society of Safety
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    • v.20 no.1 s.69
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    • pp.18-23
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    • 2005
  • This study deals with the friction and wear characteristics of C-N coated SCM415 steel. The PSII(plasma source ion implantation) apparatus was built and a SCM415 test piece with steel substrate was treated with carbon nitrogen by this apparatus. The composition and structure of the surface layer were analyzed and compared with that of PVD(physical vapor decomposition) coated TiN layer. It was found that both of friction coefficient of C-N coating and TiN coating decreased with increasing load, however, C-N coating showed relatively lower faction coefficient than that of TiN coating. The micro-vickers hardness of C-N film is 3200 Hv, which is $32\~43\%$ higher than that of TiN film. The critical load of C-N film is 52N, which is $25\%$ higher than that of TiN film. The hardness of C-N film fabricated by Plasma ion implantation is $61\~70\%$ higher than that of base material, and faction coefficient is $14\~50\%$ lower than that of base material. It is also interesting to note that the friction was changed from adhesive wear mode to light oxidizing wear mode.

Electrochemical Property of CNT/Co3O4 Nanocomposite for Anode of Lithium Batteries (리튬 이차전지 음극용 CNT/Co3O4 나노복합체의 전기화학적 특성)

  • Yoon, Dae Ho;Park, Yong Joon
    • Journal of the Korean Electrochemical Society
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    • v.17 no.3
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    • pp.187-192
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    • 2014
  • In this article, we report the fabrication and characterization of $CNT/Co_3O_4$ nanocomposite for lithium ion batteries. We expected that the composition with CNT is effective method to compensate for the low electronic conductivity of $Co_3O_4$ and suppress the stress from phase transition of $Co_3O_4$ during cycling. $CNT/Co_3O_4$ nanocomposites were composed of nano-sized $Co_3O_4$ particles, which were homogeneously distributed on the surface of CNTs. The $CNT/Co_3O_4$ electrode presented higher capacity than commercial graphite, good rate capability and stable cyclic performance. This implies that the $CNT/Co_3O_4$ could be a promising anode material for lithium ion batteries.

Synthesis of Sulfonated Hollow PP-g-Styrene Fibrous Ion-exchange Membrane and Separation of BSA Protein (술폰화 PP-g-Styrene 중공사 이온교환막의 합성과 BSA 단백질 분리에 관한 연구)

  • 황택성;이진혁
    • Polymer(Korea)
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    • v.26 no.4
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    • pp.415-421
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    • 2002
  • A sulfonated PP-g-styrene ion-exchange hollow fiber membrane was prepared by pre-irradiation method with E-beam followed by sulfonation reaction. Degree of grafting increased with the increase of styrene monomer concentration and showed the maximum value of 128% at 80% of styrene monomer composition. Sulfonation yield increased with the degree of grafting. At 100% degree of grafting, sulfonation yield showed the maximum value of 13.4%. Ion exchange capacity of sulfonated HPP-g-styrene of 3.42 meq/g was attained, resulting in the remarkable increase of adsorption ability BET analysis proved that the surface area of sulfonated HPP-g-styrene was 62.54 $m^2/g$ and the mean pore size was 25 $\AA$. From the BSA adsorption experiments, the adsorption amount of BSA was increased with sulfonation. At 13.4% sulfonation yield the adsorption amount of BSA was maximum as 3.8 mg/g. Sulfonated HPP-g-styrene was synthesized successfully and suitable for the adsorption and separation of BSA.

Preparation and Ion-Conducting Properties of New Double Comb-like Acrylonitrile Copolymers Containing Itaconate Units (이타코네이트 단위를 포함하는 새로운 이중 측쇄 아크릴로니트릴 공중합체의 제조 및 이온전도 특성 조사)

  • Lee, Chil-Won;Seol, Wan-Ho;Choi, Byung-Ku;Gong, Myoung-Seon
    • Polymer(Korea)
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    • v.25 no.4
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    • pp.602-607
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    • 2001
  • Bis(2-methoxyethyl)itaconate (bis(ME)I) was prepared for a new gel electrolyte containing double comb-like itaconate unit by esterification reaction of 2-methoxyethanol with itaconic acid. The copolymers were composed of AN/bis(ME)I = 9/1 ~ 1/1. The optimum mechanical properties and conductivity were obtained from the composition of AN/bis(ME)I = 5/1 and 6/1(25 ~ 35 wt%), LiClO4$_4$(15 wt%) and plasticizer (EC/PC = 1/1) (40 ~ 50 wt%). They showed a tough film and maintained a mechanical stability as a free standing film. The plasticized polymer gel electrolytes obtained from them showed ion conductivity of 8.12 ${\times}$ 10$_{-4}$ ~ 1.87 ${\times}$ 10$_{-3}$ S/cm. The maximum conductivity value obtained from our study was one order of magnitude higher than that of other PEO-based polymer electrolyte at ambient temperature.

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