• 제목/요약/키워드: Carboxyl groups

검색결과 236건 처리시간 0.036초

Adsorption of $\textrm{Pb}_{2+}$ in the components of bacterial cell membrane

  • Kim, Mal-Nam
    • Journal of Microbiology
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    • 제33권4호
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    • pp.278-282
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    • 1995
  • S. epidermidis cell was fractionated into cell wall, cell membrane and cytoplasm. The cell membrane adsorbed the most abundant $\textrm{Pb}_{2+}$ per unit dry weight of the three fractions tested. Adsorption behavior of $\textrm{Pb}_{2+}$ in lipid and protein, which are the main components of the cell membrane, indicated that phosphatidylethanolamine and phosphatidylinositol having phosphoryl group and gangliosides containing carboxyl groups adsorbed much more $\textrm{Pb}_{2+}$ than triglycerides lacking any chargeable functional groups. Protein purified from cell membrane adsorbed larger amount of $\textrm{Pb}_{2+}$ than total native cell membrane or cell membrane lipid.

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Coverage Dependent Adsorption and Electronic Structure of Threonine on Ge (100) Surface

  • 이명진;김기정;이한길
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제43회 하계 정기 학술대회 초록집
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    • pp.212-212
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    • 2012
  • The Coverage dependent attachment of multifunctional groups included in threonine molecules adsorbed to Ge (100)$-2{\times}1$ surface was investigated using core-level photoemission spectroscopy (CLPES) and density functional theory (DFT) calculations. The core-level spectra at a low coverage indicated that the both carboxyl and amine groups participated in the bonding with the Ge (100) surface by "O-H dissociated and N-dative bonded structure". However, at high coverage level, additional adsorption geometry of "O-H dissociation bonded structure" appeared possibly to minimize the steric hindrance between adsorbed molecules. Moreover, the C 1s, N 1s, and O 1s core level spectra confirmed that the carboxyl oxygen is more competitive against the hydroxymethyl oxygen in the adsorption reaction. The adsorption energies calculated using DFT methods suggested that four of six adsorption structures were plausible. These structures were the "O-H dissociated-N dative bonded structure", the "O-H dissociation bonded structure", the "Om-H dissociated-N dative bonded structure", and the "Om-H dissociation bonded structure" (where Om indicates the hydroxymethyl oxygen). These structures are equally likely, according to the adsorption energies alone. Conclusively, we investigate in threonine on Ge (100) surface system that the "O-H dissociated-N dative bonded structure" and the "O-H dissociation bonded structure" are preferred at low coverage and high coverage.

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Improved adsorption performance of heavy metals by surface modification of polypropylene/polyethylene media through oxygen plasma and acrylic acid

  • Hong, Jeongmin;Lee, Seungwoo;Ko, Dongah;Gwon, Eunmi;Hwang, Yuhoon
    • Membrane and Water Treatment
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    • 제11권3호
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    • pp.231-235
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    • 2020
  • Industrialization and modern developments have led to an influx of toxic heavy metals into the aquatic environment, and the accumulation of heavy metals has serious adverse effects on humans. Among the various heavy metal treatment methods, adsorption is very useful and frequently used. Plastic materials, such as polypropylene and polyethylene, have been widely used as filter media due to their mechanical and chemical stability. However, the surface of plastic material is inert and therefore the adsorption capability of heavy metals is very limited. In this study, granular media and fiber media composed of polypropylene and polyethylene are used, and the surface modification was conducted in order to increase adsorption capability toward heavy metals. Oxygen plasma generated hydroxyl groups on the surface of the media to activate the surface, and then acrylic acid was synthesized on the surface. The grafted carboxyl group was confirmed by FT-IR and SEM. Heavy metal adsorption capability of pristine and surface modified adsorbents was also evaluated. Overall, heavy metal adsorption capability was increased by surface modification due to electrostatic interaction between the carboxyl groups and heavy metal ions. Fibrous PP/PE showed lower improvement compared to granular PP media because pore blockage occurred by the surface modification step, thereby inhibiting mass transfer.

Effect of pH on Swelling Property of Hyaluronic Acid Hydrogels for Smart Drug Delivery Systems

  • Kim, Jin-Tae;Lee, Deuk-Yong;Kim, Young-Hun;Lee, In-Kyu;Song, Yo-Seung
    • 센서학회지
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    • 제21권4호
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    • pp.256-262
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    • 2012
  • Hyaluronic acid(HA) hydrogels were synthesized by immersing HA microbeads in phosphate buffered saline solutions having different pH levels to assess the effect of pH on the swelling ratio of HA hydrogels for smart drug delivery systems. No beads were formed when the HA solution(below pH 9) was crosslinked with divinyl sulfone(DVS) because DVS is a basic solution. The variation regarding the size of the microbead was not significant, suggesting that the bead size is not a function of pH(10 ~ 14). However, the pore size of the microbeads decreased with increasing pH from 10 to 14, leading to the surface smoothness and dense network as a result of higher crosslinking. The swelling ratio of hydrogels increased when the pH rose from 2(acidic) to 6(neutral). Afterwards, it decreased with further increasing pH(basic). The lower swelling ratio may be due to the lack of ionization of the carboxyl groups. On the other hand, a higher swelling ratio is likely due to the increased electrostatic repulsions between negatively charged carboxyl groups on different chains. Experimental results suggested that pH-responsive HA hydrogels can be applicable to the controlled drug delivery systems.

Mono-sodium ethylene glycolate 처리에 의한 Poly(ethylene terephthalate) Film의 물성에 관한 연구 (Study on Properties of Poly (ethylene terephthalate) Films Treated with Mono-sodium ethylene glycolate)

  • 조환;허만우;조인술;이광우;조규민
    • 한국염색가공학회지
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    • 제2권4호
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    • pp.223-230
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    • 1990
  • This study was carried out with the view of fundamental investigating to improve the tactile and the hygroscopicity of Poly (ethylene terephthalate) (PET) fibers. Mono-sodium ethylene glycolate in ethylene glycol (MSEG-EG) solution was prepared and PET films were treated with it. The following conclusions were obtained. 1. The tensile strength decreased with increasing decomposition ratio while density, crystallinity and crystallite size increased with increasing decomposition ratio when PET films were treated with MSEG-EG solution. 2. Number of carboxyl end groups was increased until 10-20% decomposition ratio when PET films were treated with MSEG-EG solution. However, the decomposition ratio became more than 20%, the number of carboxyl end groups had tendency to decreased. 3. The surface tension of PET films increased for treating with MSEC-EG solution. Hydrogen bonding force and poler force among the components of surface tension increased while dispersion force among those decreased. 4. The moisture region of PET films increased with increasing decomposition ratio when PET films were treated with MSEG-EG solution.

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Orientation Control of Polyoxometalate Nanoparticles in Organic- Inorganic Hybrid LB Films

  • Lee, Burm-Jong;Kim, Hee-Sang;Park, Dong-Ho;Nam, Sang-Hee;Yunghee Oh
    • KIEE International Transactions on Electrophysics and Applications
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    • 제4C권1호
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    • pp.26-30
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    • 2004
  • Orientation control of a polyoxometalate (POM) nanoparticle in its two-dimensional arrangement was attempted by Langmuir-Blodgett (LB) technique. For their uniorientation, two carboxyl groups were introduced on one side of the POM particle, and hydrophobic long chains were attached by esterification with the carboxyl groups (C18-POM). The C18-POM layer spread on water surface showed stability against surface pressure up to 60 mN/m. The pattern of the C18-POM isotherm was quite different from stearyl alcohol (C18-OH), while the POM itself did not show any development of surface pressure on water surface. The AFM images of C18-POM LB films showed some microcrystalline structures that were noticed as dot structures by Brewster angle microscopy. The microimages for C18-POM did not completely spread out as a monolayer on the water surface. The XPS spectra indicated the presence of POM structures and stearyl ester bonds formed from about 65% of the total carboxyls. The XRD spectra showed that the unioriented POMs were not positioned with the same lattice distance but rather in a wavy surface state.

Molecular Design for the Formation of Two-dimensional Molecular Networks: STM Study of ${\gamma}$-phenylalanine on Au(111)

  • Jeon, A-Ram;Youn, Young-Sang;Lee, Hee-Seung;Kim, Se-Hun
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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    • pp.205-205
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    • 2011
  • The self-assembly of ${\gamma}$-phenylalanine on Au(111) at 150 K was investigated using scanning tunneling microscopy (STM). Phenylalanine can potentially form two-dimensional (2D) molecular networks through hydrogen bonding (through the carboxyl and amino groups) and ${\pi}-{\pi}$ stacking interactions (via aromatic rings). We found that ${\gamma}$-phenylalanine molecules self-assembled on Au(111) surfaces into well-ordered structures such as ring-shaped clusters (at low and intermediate coverages) and 2D molecular domains (intermediate and monolayer coverages), whereas ${\alpha}$-phenylalanine molecules formed less-ordered structure on Au(111). The self-assembly of ${\gamma}$- but not ${\alpha}$-phenylalanine may be related to the flexibility of the carboxyl and amino groups in the molecule. Moreover, as expected, the 2D molecular network of ${\gamma}$-phenylalanine on Au(111) was mediated by a combination of hydrogen bonding and ${\pi}-{\pi}$ stacking interactions.

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The Influence of Functionalization of the Fe3O4 Nanoparticle on its Dispersion Property

  • Han, Jin Soon;An, Gye Seok;Park, Bong Geun;Choi, Sung-Churl
    • 한국세라믹학회지
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    • 제55권1호
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    • pp.80-84
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    • 2018
  • In this study, to improve the dispersity of $Fe_3O_4$ nanoparticles, dispersion properties were considered with various types of functionalization of $Fe_3O_4$ nanoparticles. Due to its high surface area, the electrically neutral state of its surfaces, and its magnetic momentum, $Fe_3O_4$ nanoparticles are easily aggregated in solution. In order to prevent aggregation, $Fe_3O_4$ nanoparticles were functionalized with carboxyl and amine groups in the form of a polymer compound. Carboxyl and amine groups were attached to the surface of $Fe_3O_4$ nanoparticles and the absolute value of the zeta potential was found to be enhanced by nearly 40 eV. Furthermore, the morphology and the magnetic property were analyzed for the application of $Fe_3O_4$ nanoparticles as a magnetic fluid.

보호된 이소시아네이트기와 불소화 알킬기를 가지는 아크릴계 고분자의 합성과 특성 (Synthesis and Characterization of Polyacrylate Derivatives Baying Protected Isocyanate Groups and fluorinated Alkyl Groups)

  • 김우식;김민우;정은천;백창훈;박이순;강인규;박수영
    • 폴리머
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    • 제27권4호
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    • pp.364-369
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    • 2003
  • 보호된 이소시아네이트기를 가지는 발수성 아크릴계 고분자를 합성하기 위해 개시제로 $\alpha$,$\alpha$'-아조비스이소부틸로니트릴을 사용하여 2-fluorohexylethyl acrylate (FA)와 2-(o-(1'-methylpropylidenamino)carboxyl amino)ethyl methacrylate(MEM)를 몰비를 변화시키면서 메틸 에틸 케톤 중에서 공중합하였다. 합성한 공중합체중의 MEM과 FA의 함량을 NMR로 분석하였다. 이 결과를 이용하여 Kelen-Tudos 플로트에 의해 MEM (1)과 FA (2)의 단량체 반응성비를 구하였다. 그 결과 r$_{1}$=1.59였고 r$_{2}$=0.50였다. 이들 고분자의 수평균분자량은 39400에서 72400사이에 있었고 다분산 지수는 대략 1.5정도였다. 그 고분자중의 보호된 이소시아네이트기는 15$0^{\circ}C$ 이상의 온도에서 이소시아네이트기로 재생되었다. FA를 65 ㏖% 함유하는 고분자의 물에 대한 접촉각은 95$^{\circ}$정도였다.

Sewage Sludge를 시용(施用)한 토양(土壤)에서 추출(抽出)한 수용성유기물(水溶性有機物)의 화학구조적(化學構造的) 특성(特性) (Characterization of the Water Soluble Organic Fraction Extracted from a Sewage Sludge Amended Soil)

  • 임형식
    • 한국토양비료학회지
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    • 제18권1호
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    • pp.38-49
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    • 1985
  • Sewage sludge를 시용하지 않은 토양(W), 6년간 시용한 토양($WS_6$), Swedge sludge와 토양의 혼합물을 1 주일동안 incubation한 토양( $WS_1$), 그리고 Sewage sludge (SS)로부터 각각 수용성 유기물을 추출, 정제하고 원소분석, 작용기분석을 함과 동시에 IR, UV-VIS, NMR spectroscopy에 의하여 구조적 특성을 조사하였다. SS는 W보다 H, N, P 함량이 많아서 높은 H/C비와 낮은 C/N비로 특징지워 졌으며 total acidity, carboxyl group, phenolic hydroxyl group 함량의 경우 일반적으로 SS가 가장 높았고 그 다음이 $WS_6$, $WS_1$, 그리고 W가 가장 낮았다. Aromatic character나 aromatic carboxyl group 함량은 W가 가장 크고 SS가 가장 적었으며, Aliphatic proton, aliphatic carboxyl group 함량은 SS가 가장 많고 W가 가장 적었다. 단백질 분해산물은 SS에서 풍부했고 W에서는 검출되지 않았다. NMR spectra는 SS의 수소가 W보다 다양한 functional group에 결합되어 있다는 것을 보여 주었으며 aromatic proton의 구조적 주변환경도 SS가 가장 복잡하고 그 다음이 $WS_1$, $WS_6$, 그리고 W가 비교적 단순함을 보여 주었다.

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