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Sample records for surface treated montmorillonite

  1. Probing the role of surface treated montmorillonite on the properties of semi-aromatic polyamide/clay nanocomposites

    NASA Astrophysics Data System (ADS)

    Zulfiqar, Sonia; Kausar, Ayesha; Rizwan, Muhammad; Sarwar, Muhammad Ilyas

    2008-12-01

    Semi-aromatic polyamide/organoclay nanocomposites were generated through solution blending technique. Surface modification of the montmorillonite clay was performed with p-amino benzoic acid for ample compatibilization with the polyamide matrix. The polymer chains were produced from the condensation of 4-aminophenyl sulfone with sebacoyl chloride. Interaction between the two phases was established by modifying the polymer chains with amine end groups using 1% surplus diamine near the completion of the reaction. The effect of clay dispersion and the interaction between clay and polyamide chains on the properties of nanocomposites were investigated using X-ray diffraction (XRD), transmission electron microscopy (TEM), tensile testing of thin films, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and water uptake measurements. The structural investigations confirmed the formation of delaminated nanostructures at low clay contents and disordered intercalated morphology at higher clay loadings. This morphology of the nanocomposites resulted in their enhanced mechanical and thermal properties. The tensile behavior and thermal stability significantly amplified while permeability decreased with increasing dispersibility of organoclay in the polyamide matrix.

  2. Interactions of aminomethylphosphonic acid and sarcosine with montmorillonite interlayer surfaces

    NASA Astrophysics Data System (ADS)

    Rennig, Amanda; Slutter, Annette; Tribe, Lorena

    The smectite clay, montmorillonite, can be found in many soils throughout the world. In addition to its importance in agriculture and soil remediation, montmorillonite has extensive applications in industry both in its natural form and as a component of composite materials. The adsorptive properties of montmorillonite have been explored in relation to its interactions with the common herbicide glyphosate. This herbicide, when exposed to microorganisms in the soil is degraded, forming two products: aminomethylphosphonic acid (AMPA) and sarcosine. The atomic-level interactions of these compounds with the montmorillonite interlayer surfaces are studied here using molecular mechanics. The final outcomes of these calculations are analyzed in terms of the proximity of the montmorillonite surface to the moieties of the degradation products. The phosphonate moiety was found to be the most important source of interactions for AMPA, while for sarcosine there was an even distribution between the amino and carboxylic moieties, and Na+ ion mediated surface complexes.0

  3. Monomers of cutin biopolymer: sorption and esterification on montmorillonite surfaces

    NASA Astrophysics Data System (ADS)

    Olshansky, Yaniv; Polubesova, Tamara; Chefetz, Benny

    2013-04-01

    One of the important precursors for soil organic matter is plant cuticle, a thin layer of predominantly lipids that cover all primary aerial surfaces of vascular plants. In most plant species cutin biopolymer is the major component of the cuticle (30-85% weight). Therefore cutin is the third most abundant plant biopolymer (after lignin and cellulose). Cutin is an insoluble, high molecular weight bio-polyester, which is constructed of inter-esterified cross linked hydroxy-fatty acids and hydroxyepoxy-fatty acids. The most common building blocks of the cutin are derivatives of palmitic acid, among them 9(10),16 dihydroxy palmitic acid (diHPA) is the main component. These fatty acids and their esters are commonly found in major organo-mineral soil fraction-humin. Hence, the complexes of cutin monomers with minerals may serve as model of humin. Both cutin and humin act as adsorption efficient domains for organic contaminants. However, only scarce information is available about the interactions of cutin with soil mineral surfaces, in particular with common soil mineral montmorillonite. The main hypothesize of the study is that adsorbed cutin monomers will be reconstituted on montmorillonite surface due to esterification and oligomerization, and that interactions of cutin monomers with montmorillonite will be affected by the type of exchangeable cation. Cutin monomers were obtained from the fruits of tomato (Lycopersicon esculentum). Adsorption of monomers was measured for crude Wyoming montmorillonites and montmorillonites saturated with Fe3+ and Ca2+. To understand the mechanism of monomer-clay interactions and to evaluate esterification on the clay surface, XRD and FTIR analyses of the montmorillonite-monomers complexes were performed. Our results demonstrated that the interactions of cutin monomers with montmorillonite are affected by the type of exchangeable cation. Isotherms of adsorption of cutin monomers on montmorillonites were fitted by a dual mode model of

  4. Adsorption of Crystal violet on raw and acid-treated montmorillonite, K10, in aqueous suspension.

    PubMed

    Sarma, Gautam Kumar; Sen Gupta, Susmita; Bhattacharyya, Krishna G

    2016-04-15

    Crystal violet is used as a dye in cotton and silk textiles, paints and printing ink. The dye is hazardous and exposure to it may cause permanent injury to the cornea and conjunctiva including permanent blindness, and in severe cases, may lead to respiratory and kidney failure. The present work describes removal of Crystal violet from aqueous solution by adsorption on raw and acid-treated montmorillonite, K10. The clay mineral was treated with 0.25 and 0.50 M sulfuric acid and the resulting materials were characterized by XRD, zeta potential, SEM, FTIR, cation exchange capacity, BET surface area and pore volume measurements. The influences of pH, interaction time, adsorbent amount, and temperature on adsorption were monitored and explained on the basis of physico-chemical characteristics of the materials. Basic pH generally favors adsorption but considerable removal was possible even under neutral conditions. Adsorption was very rapid and equilibrium could be attained in 180 min. The kinetics conformed to second order model. Langmuir monolayer adsorption capacity of raw montmorillonite K10 was 370.37 mg g(-1) whereas 0.25 M and 0.50 M acid treated montmorillonite K10 had capacities of 384.62 and 400.0 mg g(-1) respectively at 303 K. Adsorption was exothermic and decreased in the temperature range of 293-323 K. Thermodynamically, the process was spontaneous with Gibbs energy decreasing with rise in temperature. The results suggest that montmorillonite K10 and its acid treated forms would be suitable for removing Crystal violet from aqueous solution. PMID:26866669

  5. Ion exchange and surface charge on montmorillonite clay

    SciTech Connect

    Sperry, J.M.; Peirce, J.J.

    1999-05-01

    An ion-exchange model originally developed for pure oxides prepared in the laboratory is extended to study of ion exchange and surface charge on a naturally occurring montmorillonite clay. The range of surface charges measured for montmorillonite with various electrolyte solutions and clay pretreatments is within the range of those measured for a wide variety of oxides prepared in the laboratory, including MnO{sub 2}-IC1, MnO{sub 2}-IC12, MnO{sub 2}-IC22, titanium dioxide, ferric oxide, and aluminum oxide. In addition, fitted parameter values for lateral interaction constants and equilibrium constants for the acid sites that characterize ion exchange on montmorillonite are on the same order of magnitude as those obtained for pure oxides. Surface charge of montmorillonite in sodium nitrate solution is measured to be approximately 15 to 25% greater than that measured between a pH of 4 and 9 in calcium chloride solution. This difference is attributed to the greater charge on the calcium (2{sup +}) ion; thus, its stronger electrostatic attraction to the acid hydroxyl site. An order of magnitude change in solids concentration (C{sub p}) can lead to a difference in measured net surface charge density of the same oxide sample of several orders of magnitude. This difference increases at higher pH, indicating the importance of reporting the corresponding C{sub p} at which experiments are conducted.

  6. Silylation of montmorillonite surfaces: dependence on solvent nature.

    PubMed

    Su, Linna; Tao, Qi; He, Hongping; Zhu, Jianxi; Yuan, Peng; Zhu, Runliang

    2013-02-01

    Silylation of clay mineral surfaces has attracted much attention due to their extensive applications in materials science and environmental engineering. Silylation of montmorillonite surfaces with 3-aminopropyltriethoxysilane was carried out in polar-protic and nonpolar solvents. The swelling property of the silylated montmorillonites was investigated by intercalating with cetyltrimethylammonium bromide. Silylated montmorillonites prepared in nonpolar solvents showed a larger amount of loaded silane and a higher extent of condensation among different silane molecules, comparing with those prepared in polar-protic solvents with high dielectric constant. Meanwhile, the silylated montmorillonites prepared in nonpolar solvents displayed poor swelling property due to the linkage between silane oligomers and clay layers, that is, the neighboring clay layers were locked by the silane oligomers. The present study demonstrated that the polarity of the solvents used had an important influence on the extent of grafting, interlayer structure, and swelling property of the silylated products. This is of high importance for synthesis and application of silylated clay minerals. PMID:23123026

  7. Theoretical characterization of formamide on the inner surface of montmorillonite

    NASA Astrophysics Data System (ADS)

    Shi, Jing; Lou, Zhaoyang; Yang, Mingli; Zhang, Yao; Liu, Houbin; Meng, Yingfeng

    2014-06-01

    Density functional theory calculations were performed to characterize the low-lying structures of formamide (FA) and protonated formamide (FAH) in the interlayer space of montmorillonite (MMT). The interactions among FA/FAH, H2O, Na+, and the inner surface of MMT were systematically analyzed. The carbonyl-O of FA/FAH has strong coulomb interaction with Na+, while its amide-H forms hydrogen bonds (HBs) with water and MMT surface. The adsorption of FA is promoted by H2O, which exhibits a cooperative adsorption effect by enhancing the FA-Na+ coulomb interaction and by forming HBs with FA. Our study reveals the structural basis of FA/FAH as an intercalator for MMT splitting.

  8. First-principles study of water desorption from montmorillonite surface.

    PubMed

    Zhang, Yao; Meng, Yingfeng; Liu, Houbin; Yang, Mingli

    2016-05-01

    Knowledge about water desorption is important to give a full picture of water diffusion in montmorillonites (MMT), which is a driving factor in MMT swelling. The desorption paths and energetics of water molecules from the surface of MMT with trapped Li(+), Na(+) or K(+) counterions were studied using periodic density functional theory calculations. Two paths--surface and vacuum desorption--were designed for water desorption starting from a stationary structure in which water bonds with both the counterion and the MMT surface. Surface desorption is energetically more favorable than vacuum desorption due to water-surface hydrogen bonds that help stabilize the intermediate structure of water released from the counterion. The energy barriers of water desorption are in the order of Li(+) > Na(+) > K(+), which can be attributed to the short ionic radius of Li(+), which favors strong binding with the water molecule. The temperature dependence of water adsorption and desorption rates were compared based on the computed activation energies. Our calculations reveal that the water desorption on the MMT surface has a different mechanism from water adsorption, which results from surface effects favoring stabilization of water conformers during the desorption process. PMID:27083565

  9. Surface area of montmorillonite from the dynamic sorption of nitrogen and carbon dioxide

    USGS Publications Warehouse

    Thomas, J., Jr.; Bohor, B.F.

    1968-01-01

    Surface area determinations were made on a montmorillonite with various cations emplaced on the exchangeable sites, utilizing nitrogen and carbon dioxide as adsorbates at 77 ??K and 195 ??K, respectively, in a dynamic system. From the fraction of a Mississippi montmorillonite less than about 1 ?? in size, samples were prepared by replacing the original exchangeable cations with Li+, Na+, K+, Rb+, Cs+, Mg++, Ca++, Ba++, and NH4+, forming a series of homoionic montmorillonite species. Surface areas from 3-point B.E.T. plots (half-hour adsorption points), with nitrogen as the adsorbate, ranged from 61 m2/g for Li-montmorillonite to 138 m2/g for Cs-montmorillonite, thus reflecting a certain degree of nitrogen penetration between layers. Complete penetration should theoretically result in a surface area of over 300 m2/g for this clay with a nitrogen monolayer between each pair of platelets. The experimental data indicate that the extent of penetration is time-dependent and is also a function of the interlayer forces as governed by the size and charge of the replaceable cation. This finding negates the generally accepted concept that nitrogen at 77 ??K does not penetrate the layers and provides a measure only of the external surface of expandable clay minerals. A further measure of the variation of interlayer forces is provided by the adsorption of carbon dioxide at 195 ??K. Surface area values ranged from 99 m2/g for Li-montmorillonite to 315 m2/g for Csmontmorillonite. Although the carbon dioxide molecule is larger than the nitrogen molecule, its greater penetration apparently is a result of its being kinetically more energetic (with a larger diffusion coefficient) at its higher adsorption temperature. Similar differences have been found with both adsorbates in the study of microporous substances, such as coal, where activated diffusion is of considerable significance. ?? 1968.

  10. Influence of the intercalated cations on the surface energy of montmorillonites: consequences for the morphology and gas barrier properties of polyethylene/montmorillonites nanocomposites.

    PubMed

    Picard, E; Gauthier, H; Gérard, J-F; Espuche, E

    2007-03-15

    Organically modified montmorillonites obtained by cation exchange from the same natural layered silicate were studied. The surface properties of the pristine and a series of organically modified clays were determined by inverse gas chromatography and the water adsorption mechanisms were studied by a gravimetric technique coupled with a microcalorimeter. A significant increase of the specific surface area, a decrease of the water adsorption, and a decrease of the dispersive component of the surface energy were observed when the sodium cations of the natural montmorillonite were exchanged for a quaternary ammonium. Slighter differences in surface properties were observed, on the other hand, between the different types of organically modified montmorillonites. Indeed, similar dispersive components of the surface energy were determined on the organoclays. Nevertheless, the specific surface area increased in the range 48-80 m(2)/g with increasing d-spacing values and the presence of specific groups attached to the quaternary ammonium, such as phenyl rings or hydroxyl groups, led to some specific behaviors, i.e., a more pronounced base character and a higher water adsorption at high activity, respectively. Differences in interlayer cation chain organization, denoted as crystallinity, were also observed as a function of the nature of the chains borne by the quaternary ammonium. In a later step, polyethylene-based nanocomposites were prepared with those organically modified montmorillonites. The clay dispersion and the barrier properties of the nanocomposites were discussed as a function of the montmorillonite characteristics and of the matrix/montmorillonite interactions expected from surface energy characterization. PMID:17222420

  11. Surface properties and porous texture of montmorillonite-(Ce or Zr) phosphate cross-linked compounds

    NASA Astrophysics Data System (ADS)

    del Rey-Bueno, F.; García-Rodríguez, A.; Mata-Arjona, A.; del Rey-Pérez-Caballero, F. J.; Villafranca-Sánchez, E.

    1997-12-01

    In this work, pore texture characteristics of a series of Ce(IV) or Zr(IV) montmorillonite phosphate cross-linked compounds obtained by precipitation of cerium or zirconium phosphate with dilute H 3PO 4 on the micelles of an aqueous montmorillonite suspension, previously submitted to ion-exchange processes to replace its exchange ions with Ce(IV) or Zr(IV), are studied. Surface areas and pore volumes of the different materials prepared are determined by N 2 adsorption at 77 K and mercury porosimetry techniques. Analysis of the N 2 adsorption isotherms by the t-De Boer and Dubinin-Radushkevich methods, revealed the presence of a certain degree of microporosity in all the materials studied. Moreover, analysis of the Hg intrusion data permitted to determine the contribution of the macro- and mesopores to the total surface area and pore volume of the prepared compounds. The results reveal a greater specific surface area for these compounds than for montmorillonite and the evolution of this parameter with thermal treatment is related to the nature and content of phosphate in the different samples. However, the changes recorded in the Vp and S/ Vp parameters during the thermal process suggest that surface diffusion is the dominant transport mechanism in the sintering process.

  12. Reflectance spectroscopy of palagonite and iron-rich montmorillonite clay mixtures - Implications for the surface composition of Mars

    NASA Technical Reports Server (NTRS)

    Orenberg, James; Handy, Jonathan

    1992-01-01

    The diffuse reflectance spectra of Hawaiian palagonite mixtures with an Fe-rich montmorillonite have prompted their present use as spectral analogs of the Martian surface. Like the Mars spectrum and unlike clays, the 2.2-micron reflectance spectrum absorption band is not present in the palagonite sample; neither is the 2.2-micron Al-OH clay lattice band seen in palagonite-montmorillonite mixtures, where the latter component remains below 15 wt pct. Fe-rich montmorillonite clay may therefore be present in Mars, in combination with palagonite, while remaining undetected in remotely sensed spectra.

  13. FT-IR spectroscopic investigations of surface and intercalated 2-aminopyrimidine adsorbed on sepiolite and montmorillonite from Anatolia

    NASA Astrophysics Data System (ADS)

    Akyüz, S.; Akyüz, T.

    2003-06-01

    The adsorption of 2-amino pyrimidine (2APM) on sepiolite and montmorillonite has been investigated using FT-IR spectrometry. The intercalation of 2-amino pyrimidine within montmorillonite has been shown by X-ray diffraction to increase the interlayer spacings. 2APM interacted with montmorillonite by direct or indirect coordination (through water molecules) to the exchangeable cations. Adsorption on sepiolite was due to hydrogen bonding with surface Si-OH groups. It is concluded that endocyclic nitrogen is mainly involved in coordination. Moreover, amino group hydrogens may be involved in hydrogen bonding interaction with water molecules (NH…OH 2).

  14. Solid surface photochemistry of montmorillonite: mechanisms for the arsenite oxidation under UV-A irradiation.

    PubMed

    Yuan, Yanan; Wang, Yajie; Ding, Wei; Li, Jinjun; Wu, Feng

    2016-01-01

    Transformation of inorganic arsenic species has drawn great concern in recent decades because of worldwide and speciation-dependent pollution and the hazards that they pose to the environment and to human health. As(III) photooxidation in aquatic systems has received much attention, but little is known about photochemical transformation of arsenic species on top soil. As(III) photooxidation on natural montmorillonite under UV-A radiation was investigated by using a moisture- and temperature-controlled photochemical chamber with two black-light lamps. Initial As(III) concentration, pH, layer thickness, humic acid (HA) concentration, the presence of additional iron ions, and the contribution of reactive oxygen species (ROS) were examined. The results show that pH values of the clay layers greatly influenced As(III) photooxidation on montmorillonite. As(III) photooxidation followed the Langmuir-Hinshelwood model. HA and additional iron ions greatly promoted photooxidation, but excess Fe(II) competed with As(III) for oxidation by ROS. Scavenging experiments revealed that natural montmorillonite induced the conversion of As(III) to As(V) by generating ROS (mainly HO(•) and HO2(•)/O2(•-)) and that HO(•) radical was the predominant oxidant in this system. Our work demonstrates that photooxidation on the surface of natural clay minerals in top soil can be important to As(III) transformation. This allows understanding and predicting the speciation and behavior of arsenic on the soil surface. PMID:26194238

  15. Reflectance Spectroscopy of Palagonite and Iron-Rich Montmorillonite Clay Mixtures: Implications for the Surface Composition of Mars

    NASA Technical Reports Server (NTRS)

    Orenberg, James; Handy, Jonathan

    1992-01-01

    Mixtures of a Hawaiian palagonite and an iron-rich, montmorillonite clay (15.8 +/- 0.4 wt% Fe as Fe2O3) were evaluated as Mars surface spectral analogs from their diffuse reflectance spectra. The presence of the 2.2 microns absorption band in the reflectance spectrum of clays and its absence in the Mars spectrum have been interpreted as indicating that highly crystalline aluminous hydroxylated clays cannot be a major mineral component of the soil on Mars. The palagonite sample used in this study does not show this absorption feature in its spectrum. In mixtures of palagonite and iron-rich montmorillonite, the 2.2 microns Al-OH clay lattice band is not seen below 15 wt% montmorillonite. This suggests the possibility that iron-rich montmorillonite clay may be present in the soil of Mars at up to 15 wt% in combination with palagonite, and remain undetected in remotely sensed spectra of Mars.

  16. The electrophoretic mobility of montmorillonite. Zeta potential and surface conductivity effects.

    PubMed

    Leroy, Philippe; Tournassat, Christophe; Bernard, Olivier; Devau, Nicolas; Azaroual, Mohamed

    2015-08-01

    Clay minerals have remarkable adsorption properties because of their high specific surface area and surface charge density, which give rise to high electrochemical properties. These electrochemical properties cannot be directly measured, and models must be developed to estimate the electrostatic potential at the vicinity of clay mineral surfaces. In this context, an important model prediction is the zeta potential, which is thought to be representative of the electrostatic potential at the plane of shear. The zeta potential is usually deduced from electrophoretic measurements but for clay minerals, high surface conductivity decreases their mobility, thereby impeding straightforward interpretation of these measurements. By combining a surface complexation, conductivity and electrophoretic mobility model, we were able to reconcile zeta potential predictions with electrophoretic measurements on montmorillonite immersed in NaCl aqueous solutions. The electrochemical properties of the Stern and diffuse layers of the basal surfaces were computed by a triple-layer model. Computed zeta potentials have considerably higher amplitudes than measured zeta potentials calculated with the Smoluchowski equation. Our model successfully reproduced measured electrophoretic mobilities. This confirmed our assumptions that surface conductivity may be responsible for montmorillonite's low electrophoretic mobility and that the zeta potential may be located at the beginning of the diffuse layer. PMID:25875489

  17. Adsorption and characterization of MCPA on DDTMA- and raw-montmorillonite: Surface sites involved.

    PubMed

    Santiago, Cintia C; Fernández, Mariela A; Torres Sánchez, Rosa M

    2016-01-01

    The 4-chloro-2-methylphenoxy acid (MCPA) is an herbicide widely used in agriculture, which generates a great concern about contamination of surface water and serious consequences for human health and the environment. In this work, the adsorption of MCPA on an Argentine montmorillonite (MMT) and its organo-montmorillonite product (OMMT) with different dodecyl trimethyl ammonium loading was investigated. MCPA adsorption on OMMT increases at least 3 times, with respect to the amount determined for MMT. X-ray diffraction and zeta potential analyses indicated the inner (interlayer) and outer surface participate as adsorption sites. Changes in surface electric charge and also interlayer expansion suggest that dimethyl amine (MCPA counterion) was also surface-adsorbed. The larger aggregates of OMMT, without and with MCPA, obtained compared to those of MMT samples, generate an improvement in the coagulation efficiency. This property, particularly after MCPA retention, allows an easier separation of the solids from the solution and enables a simple technological process application. PMID:26786275

  18. Sol-gel network silica/modified montmorillonite clay hybrid nanocomposites for hydrophobic surface coatings.

    PubMed

    Meera, Kamal Mohamed Seeni; Sankar, Rajavelu Murali; Murali, Adhigan; Jaisankar, Sellamuthu N; Mandal, Asit Baran

    2012-02-01

    Sol-gel silica/nanoclay composites were prepared through sol-gel polymerization technique using tetraethylorthosilicate precursor and montmorillonite (MMT) clay in aqueous media. In this study, both montmorillonite-K(+) and organically modified MMT (OMMT) clays were used. The prepared composites were coated on glass substrate by making 1 wt% solution in ethyltrichlorosilane. The incorporation of nanoclay does not alter the intensity of characteristic Si-O-Si peak of silica network. Thermogravimetric studies show that increasing clay content increased the degradation temperature of the composites. Differential scanning calorimetry (DSC) results of organically modified MMT nanoclay incorporated composite show a shift in the melting behavior up to 38°C. From DSC thermograms, we observed that the ΔH value decreased with increasing clay loading. X-ray diffraction patterns prove the presence of nanoclay in the composite and increase in the concentration of organically modified nanoclay from 3 to 5 wt% increases the intensity of the peak at 2θ=8° corresponds to OMMT. Morphology of the control silica gel composite was greatly influenced by the incorporation of OMMT. The presence of nanoclay changed the surface of control silica gel composite into cleaved surface with brittle in nature. Contact angle measurements were done for the coatings to study their surface behavior. These hybrid coatings on glass substrate may have applications for hydrophobic coatings on leather substrate. PMID:22056084

  19. Reflectance spectroscopy of palagonite and iron-rich montmorillonite clay mixtures: Implications for the surface composition of Mars

    NASA Technical Reports Server (NTRS)

    Orenberg, J. B.; Handy, J.

    1991-01-01

    Because of the power of remote sensing reflectance spectroscopy in determining mineralogy, it was used as the major method of identifying possible mineral analogs of the Martian surface. A summary of proposed Martian surface compositions from reflectance spectroscopy before 1979 was presented. Since that time, iron-rich montmorillonite clay, nanocrystalline or nanophase hematite, and palagonite were suggested as Mars soil analog materials.

  20. Sonogashira couplings on the surface of montmorillonite-supported Pd/Cu nanoalloys.

    PubMed

    Xu, Wei; Sun, Huaming; Yu, Bo; Zhang, Guofang; Zhang, Weiqiang; Gao, Ziwei

    2014-11-26

    To explore the true identity of palladium-catalyzed Sonogashira coupling reaction, montmorillonite (MMT)-supported transition metal nanoparticles (MMT@M, M=Pd, Cu, Fe, and Ni) were prepared, characterized, and evaluated systematically. Among all MMT@M catalysts, MMT@Pd/Cu showed the highest activity, and it was successfully extended to 20 examples with 57%-97% yields. The morphology characterization of MMT@Pd/Cu revealed that the crystalline bimetallic particles were dispersed on a MMT layer as nanoalloy with diameters ranged from 10 to 11 nm. In situ IR analysis using CO as molecular probe and XPS characterization found that the surface of Pd/Cu particles consisted of both catalytic active sites of Pd(0) and Cu(I). The experiments on the catalytic activities of MMT@M found that Pd/Cu catalyst system exhibited high activity only in nanoalloy form. Therefore, the Pd/Cu nanoalloy was identified as catalyst, on which the interatom Pd/Cu transmetalation between surfaces was proposed to be responsible for its synergistic activity. PMID:25315209

  1. Structure modification of montmorillonite nanoclay by surface coating with soy protein.

    PubMed

    Jin, Minfeng; Zhong, Qixin

    2012-12-01

    To achieve exfoliated and/or intercalated structures, montmorillonite (MMT) was surface-coated by soy protein at 60 °C, at MMT/soy protein powder mass ratios of 49:1, 9:1, 4:1, and 2:1 and pH 2.0-10.0. The protein-coated MMT was triple-washed and lyophilized for characterization. Protein coating was observed at all pH conditions, based on data from X-ray diffraction, Fourier transform infrared spectroscopy, zeta potential, and quantification of protein remaining in the continuous phase and present in the triple-washed MMT. At a mass ratio of 4:1, >90% protein bound with MMT, with the largest d-spacing at pH 9.0. When the mass ratio was increased to 2:1, protein-coated MMT at pH 9.0 demonstrated the highest degree of intercalation/exfoliation, corresponding to disappearance of the diffraction peak characteristic of pristine MMT. This study thus demonstrated that intercalation/exfoliation of MMT can be easily achieved by coating with low-cost soy protein for manufacturing nanocomposite materials. PMID:23163488

  2. Selective removal and inactivation of bacteria by nanoparticle composites prepared by surface modification of montmorillonite with quaternary ammonium compounds.

    PubMed

    Khalil, Rowaida K S

    2013-10-01

    The purpose of the present study was to prepare new nanocomposites with antibacterial activities by surface modification of montmorillonite using quaternary ammonium compounds that are widely applied as disinfectants and antiseptics in food-processing environments. The intercalation of four quaternary ammonium compounds namely benzalkonium chloride, cetylpyridinium chloride monohydrate, hexadecyltrimethylammonium bromide, tetraethylammonium chloride hydrate into montmorillonite layers was confirmed by X-ray diffraction. The antibacterial influences of the modified clay variants against important foodborne pathogens differed based on modifiers quantities, microbial cell densities, and length of contact. Elution experiments through 0.1 g of the studied montmorillonite variants indicated that Staphylococcus aureus, Pseudomonas aeroginosa, and Listeria monocytogenes were the most sensitive strains. 1 g of hexadecyltrimethylammonium bromide intercalated montmorillonites demonstrated maximum inactivation of L. monocytogenes populations, with 4.5 log c.f.u./ml units of reduction. In adsorption experiments, 0.1 g of tetraethylammonium chloride hydrate montmorillonite variants significantly reduced the growth of Escherichia coli O157:H7, L. monocytogenes, and S. aureus populations by 5.77, 6.33, and 7.38 log units respectively. Growth of wide variety of microorganisms was strongly inhibited to undetectable levels (montmorillonite variants. This investigation highlights that reduction in counts of microbial populations adsorbed to the new nanocomposites was substantially different from that in elution experiments, where interactions of nanocomposites with bacteria were specific and more complex than simple ability to inactivate. Treatment columns packed with modified variants maintained their inactivation capacity to the growth of Salmonella Tennessee and S. aureus populations after 48 h of incubation

  3. Surface characteristics of thermally treated titanium surfaces

    PubMed Central

    Lee, Yang-Jin; Cui, De-Zhe; Jeon, Ha-Ra; Chung, Hyun-Ju; Park, Yeong-Joon; Kim, Ok-Su

    2012-01-01

    Purpose The characteristics of oxidized titanium (Ti) surfaces varied according to treatment conditions such as duration time and temperature. Thermal oxidation can change Ti surface characteristics, which affect many cellular responses such as cell adhesion, proliferation, and differentiation. Thus, this study was conducted to evaluate the surface characteristics and cell response of thermally treated Ti surfaces. Methods The samples were divided into 4 groups. Control: machined smooth titanium (Ti-S) was untreated. Group I: Ti-S was treated in a furnace at 300℃ for 30 minutes. Group II: Ti-S was treated at 500℃ for 30 minutes. Group III: Ti-S was treated at 750℃ for 30 minutes. A scanning electron microscope, atomic force microscope, and X-ray diffraction were used to assess surface characteristics and chemical composition. The water contact angle and surface energy were measured to assess physical properties. Results The titanium dioxide (TiO2) thickness increased as the treatment temperature increased. Additional peaks belonging to rutile TiO2 were only found in group III. The contact angle in group III was significantly lower than any of the other groups. The surface energy significantly increased as the treatment temperature increased, especially in group III. In the 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, after 24 hours of incubation, the assessment of cell viability showed that the optical density of the control had a higher tendency than any other group, but there was no significant difference. However, the alkaline phosphatase activity increased as the temperature increased, especially in group III. Conclusions Consequently, the surface characteristics and biocompatibility increased as the temperature increased. This indicates that surface modification by thermal treatment could be another useful method for medical and dental implants. PMID:22803009

  4. VERUCLAY – a new type of photo-adsorbent active in the visible light range: modification of montmorillonite surface with organic surfactant

    EPA Science Inventory

    Montmorillonite K10 was treated with VeruSOL-3, a biodegradable and food-grade surfactant mixture of coconut oil, castor oil and citrus extracts, to manufacture a benign catalytic adsorbent that is active in the visible light. Veruclay was characterized by SEM, XRD, TGA, UVDRS, a...

  5. Reflectance spectroscopy and GEX simulation of palagonite and iron-rich montmorillonite clay mixtures: Implications for the surface composition of Mars

    NASA Technical Reports Server (NTRS)

    Orenberg, J. B.; Handy, J.; Quinn, R.

    1992-01-01

    Because of the power of remote sensing reflectance spectroscopy in determining mineralogy, it has been used as the major method of identifying a possible mineral analogue of the martian surface. A summary of proposed martian surface compositions from reflectance spectroscopy before 1979 was presented by Singer et al. Since that time, iron-rich montmorillonite clay, nanocrystalline or nanophase hematite, and palagonite have been suggested as Mars soil analogue materials. Palagonite in petrological terms is best described as an amorphous, hydrated, ferric iron, silica gel. Montmorillonite is a member of the smectite clay group, and its structure is characterized by an octahedral sheet in coordination with two tetrahedral sheets in which oxygen atoms are shared. The crystal unity of montmorillonite is well defined in contrast to palagonite where it is considered amorphous or poorly crystalline at best. Because of the absence of the diagnostic strong 2.2-micron reflectance band characteristic of clays in the near-infrared (NIR) spectrum of Mars and palagonite and based upon a consideration of wide wavelength coverage (0.3-50 microns), Roush et al. concluded that palagonite is a more likely Mars surface analogue. In spite of the spectral agreement of palagonite and the Mars reflectance spectrum in the 2.2-micron region, palagonite shows poor correspondence with the results of the Viking LR experiment. In contrast, iron-rich montmorillonite clays show relatively good agreement with the results of the Viking LR experiment. This spectral study was undertaken to evaluate the spectral properties of mixtures of palagonite and Mars analogue iron-rich montmorillonite clay (16-18 wt. percent Fe as Fe2O3) as a Mars surface mineralogical model. Mixtures of minerals as Mars surface analogue materials have been studied before, but the mixtures were restricted to crystalline clays and iron oxides.

  6. Cadmium ion adsorption controls the growth of CdS nanoparticles on layered montmorillonite and calumit surfaces

    SciTech Connect

    Dekany, I.; Turi, L.; Galbacs, G.; Fendler, J.H.

    1999-05-15

    Adsorption isotherms have been determined for the intercalation of cadmium ions (Cd{sup 2+}) into layered hydrophobized montmorillonite (HDP-M) and calumit (DBS-C) sheets dispersed in ethanol (1)-cyclohexane (2) mixtures. The amount of Cd{sup 2+} adsorbed depended strongly on the composition of the binary liquid; at an ethanol mole fraction of 0.05 (x{sub 1} = 0.05), 95% of the added Cd{sup 2+} is located in the ethanolic nanoreactor at the HDP-M (or DBS-C) surface. CdS nanoparticles have been generated in situ in ethanolic nanoreactors at the HDP-M and DBS-C surfaces. Absorption spectrophotometric measurements provided information on the number of CdS nanoparticles formed and on their absorption edges, bandgaps, and mean diameters. Good correlations have been obtained between the adsorption isotherms and the size (and the amount) of the CdS formed. X-ray diffractometry established that CdS nanoparticles stretched the HDP-M and DBS-C lamellas unevenly upon intercalation.

  7. Np(V) and Pu(v) ion exchange and surface-mediated reduction mechanisms on montmorillonite.

    PubMed

    Zavarin, Mavrik; Powell, Brian A; Bourbin, Mathilde; Zhao, Pihong; Kersting, Annie B

    2012-03-01

    Due to their ubiquity and chemical reactivity, aluminosilicate clays play an important role in actinide retardation and colloid-facilitated transport in the environment. In this work, Pu(V) and Np(V) sorption to Na-montmorillonite was examined as a function of ionic strength, pH, and time. Np(V) sorption equilibrium was reached within 2 h. Sorption was relatively weak and showed a pH and ionic strength dependence. An approximate NpO(2)(+) → Na(+) Vanselow ion exchange coefficient (Kv) was determined on the basis of Np(V) sorption in 0.01 and 1.0 M NaCl solutions at pH < 5 (Kv ~ 0.3). In contrast to Np(V), Pu(V) sorption equilibrium was not achieved on the time-scale of weeks. Pu(V) sorption was much stronger than Np(V), and sorption rates exhibited both a pH and ionic strength dependence. Differences in Np(V) and Pu(V) sorption behavior are indicative of surface-mediated transformation of Pu(V) to Pu(IV) which has been reported for a number of redox-active and redox-inactive minerals. A model of the pH and ionic strength dependence of Pu(V) sorption rates suggests that H(+) exchangeable cations facilitate Pu(V) reduction. While surface complexation may play a dominant role in Pu sorption and colloid-facilitated transport under alkaline conditions, results from this study suggest that Pu(V) ion exchange and surface-mediated reduction to Pu(IV) can immobilize Pu or enhance its colloid-facilitated transport in the environment at neutral to mildly acidic pHs. PMID:22296270

  8. Adsorption of low molecular weight halocarbons by montmorillonite

    SciTech Connect

    Estes, T.J.; Shah, R.V.; Vilker, V.L. )

    1988-04-01

    Montmorillonite clay from Clay Spur, WY, was found to adsorb several low molecular weight, hydrophobic halocarbons from aqueous solution at sub-parts-per-million levels. The halocarbons studied were trichloroethylene, tetrachloroethylene, hexachloroethane, and dibromochloropropane. When the montmorillonite was treated with sodium citrate-bicarbonate-dithionite (CBD), it adsorbed higher levels of halocarbons than the untreated clay. In addition, the CBD-treated clay exhibited a maximum in halocarbon adsorption around pH 4, while untreated clay showed little variation in adsorption over the pH range 2-10. Adsorption of trichloroethylene was inhibited by low concentrations of sodium chloride (0.01 M or greater) in solution. Aging the CBD-treated clay in water decreased its capacity to adsorb trichloroethylene. Desorption studies showed that the sorption of tetrachloroethylene to CBD-treated clay is an irreversible process when compared to sorption by fumed silica. The ability of montmorillonite to adsorb halocarbons and the instability of the clay in water are postulated to involve changes in the oxide surface coating on the clay.

  9. Surface properties of in situ organo-montmorillonite modified wood flour and the influence on mechanical properties of composites with polypropylene

    NASA Astrophysics Data System (ADS)

    Liu, Ru; Sun, Wenjing; Cao, Jinzhen; Wang, Jiamin

    2016-01-01

    In this study, wood flours (WFs) were modified by sodium-montmorillonite (Na-MMT) and didecyl dimethyl ammonium chloride (DDAC) in two steps to form organo-montmorillonite (OMMT) inside WFs at different OMMT concentrations (0.25, 0.5, 0.75 and 1%, respectively). The surface properties of WFs were investigated as an approach to understand the compatibility of WF/polypropylene (PP) composites. The mechanical properties of the composites were also tested. The results showed that: (1) OMMT modification did not influence the surface morphologies of WFs; (2) owing to the covering of OMMT on WF surface, with increasing OMMT concentration, the surface free energies of WFs increased with both increases of dispersive and polar components, and the surface hydroxyl groups of WF decreased, suggesting good compatibility with non-polar PP; (3) the flexural and tensile strength were correlated with the dispersive component fraction. Significant improvements in flexural and tensile strength were found at OMMT concentration of 0.5%. With increase of OMMT concentration, the flexural and Young's modulus increased. However, the impact strength decreased.

  10. Perovskite LaFeO3/montmorillonite nanocomposites: synthesis, interface characteristics and enhanced photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Peng, Kang; Fu, Liangjie; Yang, Huaming; Ouyang, Jing

    2016-01-01

    Perovskite LaFeO3/montmorillonite nanocomposites (LaFeO3/MMT) have been successfully prepared via assembling LaFeO3 nanoparticles on the surface of montmorillonite with citric acid assisted sol-gel method. The results indicated that the uniform LaFeO3 nanoparticles were densely deposited onto the surface of montmorillonite, mainly ranging in diameter from 10 nm to 15 nm. The photocatalytic activity of LaFeO3/MMT was evaluated by the degradation of Rhodamine B (RhB) under visible light irradiation, indicating that LaFeO3/MMT exhibited remarkable adsorption efficiency and excellent photocatalytic activity with the overall removal rate of RhB up to 99.34% after visible light irradiation lasting for 90 min. The interface characteristic and possible degradation mechanism were explored. The interface characterization of LaFeO3/MMT suggested that LaFeO3 nanoparticles could be immobilized on the surface of montmorillonite with the Si-O-Fe bonds. The abundant hydroxyl groups of montmorillonite, semiconductor photocatalysis of LaFeO3 and Fenton-like reaction could enhance the photocatalytic degradation through a synergistic effect. Therefore, the LaFeO3/MMT is a very promising photocatalyst in future industrial application to treat effectively wastewater of dyes.

  11. Perovskite LaFeO3/montmorillonite nanocomposites: synthesis, interface characteristics and enhanced photocatalytic activity.

    PubMed

    Peng, Kang; Fu, Liangjie; Yang, Huaming; Ouyang, Jing

    2016-01-01

    Perovskite LaFeO3/montmorillonite nanocomposites (LaFeO3/MMT) have been successfully prepared via assembling LaFeO3 nanoparticles on the surface of montmorillonite with citric acid assisted sol-gel method. The results indicated that the uniform LaFeO3 nanoparticles were densely deposited onto the surface of montmorillonite, mainly ranging in diameter from 10 nm to 15 nm. The photocatalytic activity of LaFeO3/MMT was evaluated by the degradation of Rhodamine B (RhB) under visible light irradiation, indicating that LaFeO3/MMT exhibited remarkable adsorption efficiency and excellent photocatalytic activity with the overall removal rate of RhB up to 99.34% after visible light irradiation lasting for 90 min. The interface characteristic and possible degradation mechanism were explored. The interface characterization of LaFeO3/MMT suggested that LaFeO3 nanoparticles could be immobilized on the surface of montmorillonite with the Si-O-Fe bonds. The abundant hydroxyl groups of montmorillonite, semiconductor photocatalysis of LaFeO3 and Fenton-like reaction could enhance the photocatalytic degradation through a synergistic effect. Therefore, the LaFeO3/MMT is a very promising photocatalyst in future industrial application to treat effectively wastewater of dyes. PMID:26778180

  12. Perovskite LaFeO3/montmorillonite nanocomposites: synthesis, interface characteristics and enhanced photocatalytic activity

    PubMed Central

    Peng, Kang; Fu, Liangjie; Yang, Huaming; Ouyang, Jing

    2016-01-01

    Perovskite LaFeO3/montmorillonite nanocomposites (LaFeO3/MMT) have been successfully prepared via assembling LaFeO3 nanoparticles on the surface of montmorillonite with citric acid assisted sol-gel method. The results indicated that the uniform LaFeO3 nanoparticles were densely deposited onto the surface of montmorillonite, mainly ranging in diameter from 10 nm to 15 nm. The photocatalytic activity of LaFeO3/MMT was evaluated by the degradation of Rhodamine B (RhB) under visible light irradiation, indicating that LaFeO3/MMT exhibited remarkable adsorption efficiency and excellent photocatalytic activity with the overall removal rate of RhB up to 99.34% after visible light irradiation lasting for 90 min. The interface characteristic and possible degradation mechanism were explored. The interface characterization of LaFeO3/MMT suggested that LaFeO3 nanoparticles could be immobilized on the surface of montmorillonite with the Si-O-Fe bonds. The abundant hydroxyl groups of montmorillonite, semiconductor photocatalysis of LaFeO3 and Fenton-like reaction could enhance the photocatalytic degradation through a synergistic effect. Therefore, the LaFeO3/MMT is a very promising photocatalyst in future industrial application to treat effectively wastewater of dyes. PMID:26778180

  13. Elaboration et caracterisation de nanocomposites polyethylene/montmorillonite

    NASA Astrophysics Data System (ADS)

    Stoeffler, Karen

    This research project consists in preparing polyethylene/montmorillonite nanocomposites for film packaging applications. Montmorillonite is a natural clay with an exceptional aspect ratio. In recent years, its incorporation in polymer matrices has attracted great interest. The pioneer work from Toyota on polyamide-6/montmorillonite composites has shown that it was possible to disperse the clay at a nanometric scale. Such a structure, so-called exfoliated, leads to a significant increase in mechanical, barrier and fire retardant properties, even at low volumetric fractions of clay. This allows a valorization of the polymeric material at moderate cost. Due to its high polarity, montmorilloite exfoliation in polymeric matrices is problematic. In the particular case of polyolefin matrices, the platelets dispersion remains limited: most frequently, the composites obtained exhibit conventional structures (microcomposites) or intercalated structures. To solve this problem, two techniques are commonly employed: the surface treatment of the clay, which allows the expansion of the interfoliar gallery while increasing the affinity between the clay and the polymer, and the use of a polar compatibilizing agent (grafted polyolefin). The first part of this thesis deals with the preparation and the characterization of highly thermally stable organophilic montmorillonites. Commercial organophilic montmorillonites are treated with quaternary ammonium intercalating agents. However, those intercalating agents present a poor thermal stability and are susceptible to decompose upon processing, thus affecting the clay dispersion and the final properties of the nanocomposites. In this work, it was proposed to modify the clay with alkyl pyridinium, alkyl imidazolium and alkyl phosphonium intercalating agents, which are more stable than ammonium based cations. Organophilic montmorillonites with enhanced thermal stabilites compared to commercial organoclays (+20°C to +70°C) were prepared

  14. NANOFILTRATION FOULANTS FROM A TREATED SURFACE WATER

    EPA Science Inventory

    The foulant from pilot nanofiltration membrane elements fed conventionally-treated surface water for 15 months was analyzed for organic, inorganic, and biological parameters. The foulant responsible for flux loss was shown to be a film layer 20 to 80 um thick with the greatest de...

  15. Reflectance spectroscopy of ferric sulfate-bearing montmorillonites as Mars soil analog materials

    NASA Technical Reports Server (NTRS)

    Bishop, J. L.; Pieters, C. M.; Burns, R. G.; Edwards, J. O.; Mancinelli, R. L.; Froschl, H.

    1995-01-01

    Spectroscopic analyses have shown that smectites enhanced in the laboratory with additional ferric species exhibit important similarities to those of the soils on Mars. Ferrihydrite in these chemically treated smectites has features in the visible to near-infrared region that resemble the energies and band strengths of features in reflectance spectra observed for several bright regions on Mars. New samples have been prepared with sulfate as well, because S was found by Viking to be a major component in the surface material on Mars. A suite of ferrihydrite-bearing and ferric sulfate-bearing montmorillonites, prepared with variable Fe3+ and S concentrations and variable pH conditions, has been analyzed using reflectance spectroscopy in the visible and infrared regions, Mossbauer spectroscopy at room temperature and 4 K, differential thermal analysis, and X-ray diffraction. These analyses support the formation of ferrihydrite of variable crystallinity in the ferrihydrite-bearing montmorillonites and a combination of schwertmannite and ferrihydrite in the ferric sulfate-bearing montmorillonites. Small quantities of poorly crystalline or nanophase forms of other ferric materials may also be present in these samples. The chemical formation conditions of the ferrihydrite-bearing and ferric sulfate-bearing montmorillonites influence the character of the low temperature Mossbauer sextets and the visible reflectance spectra. An absorption minimum is observed at 0.88-0.89 micrometers in spectra of the ferric sulfate-bearing samples, and at 0.89-0.92 micrometers in spectra of the ferrihydrate-bearing montmorillonites. Mossbauer spectra of the ferric sulfate-bearing montmorillonites indicate variable concentrations of ferrihydrite and schwertmannite in the interlaminar spaces and along grain surfaces. Dehydration under reduced atmospheric pressure conditions induces a greater effect on the adsorbed and interlayer water in ferrihydrite-bearing montmorillonite than on the water

  16. Sorption of trivalent lanthanides and actinides onto montmorillonite: Macroscopic, thermodynamic and structural evidence for ternary hydroxo and carbonato surface complexes on multiple sorption sites.

    PubMed

    Fernandes, M Marques; Scheinost, A C; Baeyens, B

    2016-08-01

    The credibility of long-term safety assessments of radioactive waste repositories may be greatly enhanced by a molecular level understanding of the sorption processes onto individual minerals present in the near- and far-fields. In this study we couple macroscopic sorption experiments to surface complexation modelling and spectroscopic investigations, including extended X-ray absorption fine structure (EXAFS) and time-resolved laser fluorescence spectroscopies (TRLFS), to elucidate the uptake mechanism of trivalent lanthanides and actinides (Ln/An(III)) by montmorillonite in the absence and presence of dissolved carbonate. Based on the experimental sorption isotherms for the carbonate-free system, the previously developed 2 site protolysis non electrostatic surface complexation and cation exchange (2SPNE SC/CE) model needed to be complemented with an additional surface complexation reaction onto weak sites. The fitting of sorption isotherms in the presence of carbonate required refinement of the previously published model by reducing the strong site capacity and by adding the formation of Ln/An(III)-carbonato complexes both on strong and weak sites. EXAFS spectra of selected Am samples and TRLFS spectra of selected Cm samples corroborate the model assumptions by showing the existence of different surface complexation sites and evidencing the formation of Ln/An(III) carbonate surface complexes. In the absence of carbonate and at low loadings, Ln/An(III) form strong inner-sphere complexes through binding to three Al(O,OH)6 octahedra, most likely by occupying vacant sites in the octahedral layers of montmorillonite, which are exposed on {010} and {110} edge faces. At higher loadings, Ln/An(III) binds to only one Al octahedron, forming a weaker, edge-sharing surface complex. In the presence of carbonate, we identified a ternary mono- or dicarbonato Ln/An(III) complex binding directly to one Al(O,OH)6 octahedron, revealing that type-A ternary complexes form with the one

  17. Surface modification of montmorillonite on surface Acid-base characteristics of clay and thermal stability of epoxy/clay nanocomposites.

    PubMed

    Park, Soo-Jin; Seo, Dong-Il; Lee, Jae-Rock

    2002-07-01

    In this work, the effect of surface treatments on smectitic clay was investigated in surface energetics and thermal behaviors of epoxy/clay nanocomposites. The pH values, X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FT-IR) were used to analyze the effect of cation exchange on clay surface and the exfoliation phenomenon of clay interlayer. The surface energetics of clay and thermal properties of epoxy/clay nanocomposites were investigated in contact angles and thermogravimetric analysis (TGA), respectively. From the experimental results, the surface modification of clay by dodecylammonium chloride led to the increases in both distance between silicate layers of about 8 A and surface acid values, as well as in the electron acceptor component (gamma(+)(s)) of surface free energy, resulting in improved interfacial adhesion between basic (or electron donor) epoxy resins and acidic (electron acceptor) clay interlayers. Also, the thermal stability of nanocomposites was highly superior to pure epoxy resin due to the presence of the well-dispersed clay nanolayer, which has a barrier property in a composite system. PMID:16290714

  18. Ferric sulfate montmorillonites as Mars soil analogs

    NASA Technical Reports Server (NTRS)

    Bishop, J. L.; Pieters, C. M.; Burns, R. G.

    1993-01-01

    Spectroscopic analyses have shown that Fe(3+)-doped smectites prepared in the laboratory exhibit important similarities to the soils on Mars. Ferrihydrite in these smectites has features in the visible to near-infrared region that resemble the energies and band-strengths of features in reflectance spectra observed for several bright regions on Mars. Ferric - sulfate - montmorillonite samples have been prepared more recently because they are a good compositional match with the surface material on Mars as measured by Viking. Reflectance spectra of montmorillonite doped with ferric sulfate in the interlayer regions include a strong 3 micron band that persists under dry conditions. This is in contrast to spectra of similarly prepared ferric-doped montmorillonites, which exhibit a relatively weaker 3 micron band under comparable dry environmental conditions. Presented here are reflectance spectra of a suite of ferric-sulfate exchanged montmorillonites prepared with variable ferric sulfate concentrations and variable pH conditions.

  19. Surface characterizations of variously treated titanium materials.

    PubMed

    Lim, Y J; Oshida, Y; Andres, C J; Barco, M T

    2001-01-01

    The attachment of cells to titanium surfaces is an important phenomenon in the area of clinical implant dentistry. A major consideration in designing implants has been to produce surfaces that promote desirable responses in the cells and tissues. To achieve these requirements, the titanium implant surface can be modified in various ways. This research was designed to elucidate the relationship between surface roughness (Ra) and contact angle (theta) of various engineered titanium surfaces of commercially pure titanium, titanium-aluminum-vanadium alloy (Ti-6Al-4V), and titanium-nickel (TiNi) alloy. The contact angle was measured using distilled water, 1% sodium chloride solution, human neutrophils, and osteoblast-like cells. Surface oxide crystallography was identified by transmission electron diffraction. It was found that: (1) there were no significant differences in contact angles among the 4 media; (2) for commercially pure titanium, a combined treatment (hydrofluoric acid/nitric acid/water --> sodium hydroxide --> oxidation) showed the lowest theta (10.51 degrees in water), while the surface treated with sulfuric acid showed the highest value (72.99 degrees in water); (3) for all commercially pure titanium samples, when theta is greater than 45 degrees, the contact angle increases linearly with Ra (hydrophobic nature) and the surface is covered with rutile-type oxide only, while the contact angle decreases linearly with Ra when theta is less than 45 degrees (hydrophilic nature) and the surface is covered with a mixture of rutile and anatase oxides; and (4) a similar trend was found on Ti-6Al-4V and TiNi surfaces. PMID:11432653

  20. Dispersibility of Amphibious Montmorillonite

    NASA Astrophysics Data System (ADS)

    Yeh, Meng-Heng; Hwang, Weng-Sing; Kuo, Wuei-Jueng

    2005-09-01

    The objective of this study is to develop a suitable method to convert hydrophilic montmorillonite into amphibious montmorillonite by replacing the sodium ions normally found in clay with poly(oxyethylene) (POE)-amide chlorite cations. Amphibious montmorillonite has a high d-spacing and good dispersion characteristics in many different types of solutions, including those having an intermediate hydrophilic lipophilic balance (HLB) value. Four different modifying cations are tested and X-ray diffraction analysis is performed to measure the resulting changes in the d-spacing of the MMT. Scanning electron microscopy is employed to investigate the morphology of the modified clays. A laser-doppler particle analyzer is used to measure the particle size of the clays in various solutions. Dobrat’s method is applied to calculate the dispersibility of each clay and Stoke’s law is used to evaluate the settling rate. The results indicate that the d-spacing of the POE-amide chlorite cation modified montmorillonite increases from 1.28 to 3.51 nm. The amphibious montmorillonite demonstrates good dispersion characteristics in eight commonly employed coating solutions with intermediate HLB values.

  1. Peptide Therapeutics for Treating Ocular Surface Infections

    PubMed Central

    2014-01-01

    Abstract Microbial pathogens—bacteria, viruses, fungi, and parasites—are significant causes of blindness, particularly in developing countries. For bacterial and some viral infections a number of antimicrobial drugs are available for therapy but there are fewer available for use in treating fungal and parasitic keratitis. There are also problems with current antimicrobials, such as limited efficacy and the presence of drug-resistant microbes. Thus, there is a need to develop additional drugs. Nature has given us an example of 1 potential source of new antimicrobials: antimicrobial peptides and proteins that are either present in bodily fluids and tissues constitutively or are induced upon infection. Given the nature of peptides, topical applications are the most likely use to be successful and this is ideal for treating keratitis. Such peptides would also be active against drug-resistant pathogens and might act synergistically if used in combination therapy. Hundreds of peptides with antimicrobial properties have been isolated or synthesized but only a handful have been tested against ocular pathogens and even fewer have been tested in animal models. This review summarizes the currently available information on the use of peptides to treat keratitis, outlines some of the problems that have been identified, and discusses future studies that will be needed. Most of the peptides that have been tested have shown activity at concentrations that do not warrant further development, but 1 or 2 have promising activity raising the possibility that peptides can be developed to treat keratitis. PMID:25250986

  2. Treating Surfaces To Obtain Narrowband Thermal Emission

    NASA Technical Reports Server (NTRS)

    Burger, Dale R.; Ong, Tiong P.

    1993-01-01

    Surfaces emitting electromagnetic radiation predominantly in desired narrow spectral bands when heated made more durable, and fabricated less expensively, according to proposal. Narrowband thermal emitters made by polishing metal substrates to specularity, then coating specular surfaces with films of rare-earth oxides approximately less than 1 micrometer thick. Metal substrates inherently resistant to mechanical shock. Resistance to thermal shock achieved by choosing metals and rare-earth oxides having equal or nearly equal coefficients of thermal expansion.

  3. Modeling the Adsorption of Oxalate onto Montmorillonite.

    PubMed

    Ramos, M Elena; Emiroglu, Caglayan; García, David; Sainz-Díaz, C Ignacio; Huertas, F Javier

    2015-11-01

    In this work, a multiscale modeling of the interaction of oxalate with clay mineral surfaces from macroscale thermodynamic equilibria simulations to atomistic calculations is presented. Previous results from macroscopic adsorption data of oxalate on montmorillonite in 0.01 M KNO3 media at 25 °C within the pH range from 2.5 to 9 have been used to develop a surface complexation model. The experimental adsorption edge data were fitted using the triple-layer model (TLM) with the aid of the FITEQL 4.0 computer program. Surface complexation of oxalate is described by two reactions: >AlOH + Ox(2-) + 2H(+) = >AlOxH + H2O (log K = 14.39) and >AlOH + Ox(2-) + H(+) = >AlOx(-) + H2O (log K = 10.39). The monodentate complex >AlOxH dominated adsorption below pH 4, and the bidentate complex >AlOx(-) was predominant at higher pH values. Both of the proposed inner-sphere oxalate species are qualitatively consistent with previously published diffuse reflectance FTIR spectroscopic results for oxalate on montmorillonite edge surface (Chem. Geol. 2014, 363, 283-292). Atomistic computational studies have been performed to understand the interactions at the molecular level between adsorbates and mineral surface, showing the atomic structures and IR frequency shifts of the adsorption complexes of oxalate with the edge surface of a periodic montmorillonite model. PMID:26444928

  4. Montmorillonite Dissolution in Simulated Lung Fluids

    NASA Astrophysics Data System (ADS)

    Schmidt, M.; Wendlandt, R. F.

    2008-12-01

    Because lung fluids" first interaction is with the surface of inhaled grains, the surface properties of inhaled mineral dusts may have a generally mitigating effect on cytotoxicity and carcinogenicity. Wendlandt et al. (Appl. Geochem. 22, 2007) investigated the surface properties of respirable-sized quartz grains in bentonites and recognized pervasive montmorillonite surface coatings on silica grains. The purpose of this study was to determine the dissolution rate and biodurability of montmorillonite in simulated lung fluids and to assess its potential to mitigate silica cytotoxicity. Modified batch reaction experiments were conducted on purified and size fractionated calcic (SAz-2; 0.4-5 μm) and sodic (DC-2; 0.4-2 μm) montmorillonites for 120 to 160 days of reaction time at 37°C in both simulated extracellular lung fluid (Lu) and simulated lysosomal fluid (Ly). Modified batch experiments simulated a flow-through setup and minimized sample handling difficulties. Reacted Lu and Ly fluid was analyzed for Mg, Al, and Si on an ICP-OE spectrometer. Steady state dissolution was reached 90-100 days after the start of the experiment and maintained for 40-60 days. Measured montmorillonite dissolution rates based on BET surface areas and Si steady state release range from 4.1x10-15 mol/m2/s at the slowest to 1.0x10-14 mol/m2/s at the fastest with relative uncertainties of less than 10%. Samples reacting in Ly (pH = 4.55) dissolved faster than those in Lu (pH = 7.40), and DC-2 dissolved faster than SAz-2. The measured range of biodurabilities was 1,300 to 3,400 years for a 1 μm grain assuming a spherical volume and a molar volume equal to that of illite. The difference in salinities of the two fluids was too slight to draw conclusions about the relationship of ionic strength to dissolution rate. Results indicate that montmorillonite dissolution is incongruent and edge controlled. Dissolution rates for DC- 2 and SAz-2 clays were comparable to those reported in the

  5. Material, Mechanical, and Tribological Characterization of Laser-Treated Surfaces

    NASA Astrophysics Data System (ADS)

    Yilbas, Bekir Sami; Kumar, Aditya; Bhushan, Bharat; Aleem, B. J. Abdul

    2014-10-01

    Laser treatment under nitrogen assisting gas environment of cobalt-nickel-chromium-tungsten-based superalloy and high-velocity oxygen-fuel thermal spray coating of nickel-chromium-based superalloy on carbon steel was carried out to improve mechanical and tribological properties. Superalloy surface was preprepared to include B4C particles at the surface prior to the laser treatment process. Material and morphological changes in the laser-treated samples were examined using scanning electron microscopy, energy-dispersive spectroscopy, and x-ray diffraction (XRD) analysis. Residual stresses present at the surface region of the laser-treated layer were determined from the XRD data. The microhardness of the laser-treated surface was measured by indentation tests. Fracture toughness of the coating surfaces before and after laser treatment were also measured using overload indentation tests. Macrowear and macrofriction characterization were carried out using pin-on-disk tests.

  6. Sol-gel hybrid films based on organosilane and montmorillonite for corrosion inhibition of AA2024.

    PubMed

    Dalmoro, V; dos Santos, J H Z; Armelin, E; Alemán, C; Azambuja, D S

    2014-07-15

    The present work reports the production of films on AA2024-T3 composed of vinyltrimethoxysilane (VTMS)/tetraethylorthosilicate (TEOS) with incorporation of montmorillonite (sodium montmorillonite and montmorillonite modified with quaternary ammonium salt, abbreviated Na and 30B, respectively), generated by the sol-gel process. According to FT-IR analyses the incorporation of montmorillonite does not affect silica network. Electrochemical characterization was performed by electrochemical impedance spectroscopy measurement in 0.05 mol L(-1) NaCl solution. Results indicate that montmorillonite incorporation improves the corrosion protection compared to the non-modified system. Scanning electron microscopy micrographs reveal that high concentrations of montmorillonite provide agglomerations on the metallic surface, which is in detriment of the anticorrosive performance. The VTMS/TEOS/30B films with the lowest concentration (22 mg L(-1)) of embedded clay provide the highest corrosion protection. PMID:24863798

  7. Analysis of peptides synthesized in the presence of SAz-1 montmorillonite and Cu(2+) exchanged hectorite.

    PubMed

    Porter, T L; Eastman, M P; Bain, E; Begay, S

    2001-07-01

    We have investigated the synthesis of oligopeptides containing glycine and tyrosine in the presence of the clay minerals montmorillonite (non-exchanged, SAz-1) and Cu(2+) exchanged hectorite. In both cases, homopolymers of the two amino acids are formed, as are mixed peptides. In the case of Cu(2+) hectorite, mixed oligopeptides up to trimers are detected in small amounts. For montmorillonite, heterogeneous oligopeptides up to hexamers are detected. Our experiments indicate montmorillonite is more effective in promoting oligopeptide formation than Cu(2+) hectorite. Analysis of the oligopeptide sequences formed on the montmorillonite surfaces indicates preferential synthesis of certain Gly-Tyr sequences over others. PMID:11429201

  8. Aflatoxin Toxicity Reduction in Feed by Enhanced Binding to Surface-Modified Clay Additives

    PubMed Central

    Jaynes, William F.; Zartman, Richard E.

    2011-01-01

    Animal feeding studies have demonstrated that clay additives, such as bentonites, can bind aflatoxins in ingested feed and reduce or eliminate the toxicity. Bentonite deposits are found throughout the world and mostly consist of expandable smectite minerals, such as montmorillonite. The surfaces of smectite minerals can be treated with organic compounds to create surface-modified clays that more readily bind some contaminants than the untreated clay. Montmorillonites treated with organic cations, such as hexadecyltrimethylammonium (HDTMA) and phenyltrimethylammonium (PTMA), more effectively remove organic contaminants, such as benzene and toluene, from water than untreated clay. Similarly, montmorillonite treated with PTMA (Kd = 24,100) retained more aflatoxin B1 (AfB1) from aqueous corn flour than untreated montmorillonite (Kd = 944). Feed additives that reduced aflatoxin toxicity in animal feeding studies adsorbed more AfB1 from aqueous corn flour than feed additives that were less effective. The organic cations HDTMA and PTMA are considered toxic and would not be suitable for clay additives used in feed or food, but other non-toxic or nutrient compounds can be used to prepare surface-modified clays. Montmorillonite (SWy) treated with choline (Kd = 13,800) and carnitine (Kd = 3960) adsorbed much more AfB1 from aqueous corn flour than the untreated clay (Kd = 944). A choline-treated clay prepared from a reduced-charge, high-charge montmorillonite (Kd = 20,100) adsorbed more AfB1 than the choline-treated high-charge montmorillonite (Kd = 1340) or the untreated montmorillonite (Kd = 293). Surface-modified clay additives prepared using low-charge smectites and nutrient or non-toxic organic compounds might be used to more effectively bind aflatoxins in contaminated feed or food and prevent toxicity. PMID:22069725

  9. Surface treated polypropylene (PP) fibres for reinforced concrete

    SciTech Connect

    López-Buendía, Angel M.; Romero-Sánchez, María Dolores; Climent, Verónica

    2013-12-15

    Surface treatments on a polypropylene (PP) fibre have contributed to the improvement of fibre/concrete adhesion in fibre-reinforced concrete. The treatments to the PP fibre were characterized by contact angle measurements, ATR-IR and XPS to analyse chemical alterations. The surface topography and fibre/concrete interaction were analysed by several microscopic techniques, namely optical petrographic, and scanning electron microscopy. Treatment modified the surface chemistry and topography of the fibre by introducing sodium moieties and created additional fibre surface roughness. Modifications in the fibre surface led to an increase in the adhesion properties between the treated fibres and concrete and an improvement in the mechanical properties of the fibre-reinforced concrete composite as compared to the concrete containing untreated PP fibres. Compatibility with the concrete and increased roughness and mineral surface was also improved by nucleated portlandite and ettringite mineral association anchored on the alkaline PP fibre surface, which is induced during treatment.

  10. Biocompatibility Evaluation of Nanosecond Laser Treated Titanium Surfaces

    NASA Astrophysics Data System (ADS)

    Honda, Ryo; Mizutani, Masayoshi; Ohmori, Hitoshi; Komotori, Jun

    We developed surface modification technologies for dental implants in this study. The study contributes to shortening the time required for adhesion between alveolar bone and fixtures which consist of dental implants. A Nd:YVO4 nanosecond laser was used to modify the surfaces of commercially pure titanium (CP Ti) disks, and their biocompatibility was evaluated cytocompatibility and bioactivity. First, rows of 200 µm spaced rectilinear laser treatments were performed on surfaces of CP Ti disks. Osteoblasts derived from rat mesenchymal stem cells were then cultured on the treated surfaces. Cytocompatibility on the laser treated area was evaluated by observing adhesion behavior of cells on these surfaces. The results indicated that the micro-order structure formed by the laser treatment promoted adhesion of osteoblasts and that traces of laser treatment without microstucture didn't affect the adhesion. Second, surfaces of CP Ti disks were completely covered by traces of laser treatment, which created complex microstructures of titania whose crystal structure is rutile and anatase. This phenomenon allowed the creation of hydroxyapatite on the surface of the disks in 1.5-times simulated body fluid (1.5SBF) while no hydroxyapatite was observed on conventional polished surfaces in the same conditions. This result indicates that bioactivity was enabled on CP Ti by the laser treatment. From these two results, laser treatment for CP Ti surfaces is an effective method for enhancing adhesion of osteoblasts and promoting bioactivity, which are highly appreciated properties for dental implants.

  11. Adsorption of ferrous ions onto montmorillonites

    NASA Astrophysics Data System (ADS)

    Qin, Dawei; Niu, Xia; Qiao, Min; Liu, Gang; Li, Hongxin; Meng, Zhenxiao

    2015-04-01

    The adsorption of Fe (II) onto montmorillonites was investigated through initial concentration, contact time, pH and temperature. During the whole adsorption process, the ascorbic acid (Vitamin C) was added as a kind of antioxidant, at the same time, deionized water (after boiling) and nitrogen protection were also used to avoid oxidation. The Fe2+/Fetotal ratio of the iron exists in the Fe-montmorillonites was found more than 95%. Two kinetic models, including pseudo-first-order and pseudo-second-order model, were used to analyze the adsorption process of Fe (II) on montmorillonites. The results of our study showed that adsorption process fitted with pseudo-second-order well. Adsorption isotherms showed that Langmuir model was better than Freundlich model. The thermodynamic parameters ΔG0 and ΔH0 were 3.696 kJ/mol and 6.689 kJ/mol (we just gave the values at 298 K), respectively. The positive values at different temperatures showed that the adsorption process was non-spontaneous and endothermic. The characteristics of materials were determined by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Surface area and porosity analyzer, Thermogravimetric analysis (TGA), Differential scanning calorimeter (DSC) and Zeta potential distribution.

  12. [Adsorptive Stabilization of Soil Cr (VI) Using HDTMA Modified Montmorillonite].

    PubMed

    2016-03-15

    A series of organo-montomorillonites were prepared using Na-montomorillonite and hexadecyl trimethyl ammonium bromide (HDTMA). The organo-montomorillonites were then investigated for the remediation of Cr(VI) contaminated soils. FT-IR, XRD, SEM and N2 -BET, CEC, Zeta potential measurement were conducted to understand the structural changes of montmorillonites as different amounts of HDTMAs were added as modifier. The characterization results indicated that the clay interlayer spacing distance increased from 1. 25 nm to 2. 13 nm, the clay surface roughness decreased, the clay surface area reduced from 38.91 m² · g⁻¹ to 0.42 m² · g⁻¹, the clay exchangeable cation amount reduced from 62 cmol · kg⁻¹ to 9.9 cmol · kg⁻¹ and the clay surface charge changed from -29.1 mV to 5.59 mV as the dosage of HDTMA in montmorillonite was increased. The TCLP (toxicity characteristic leaching procedure) was used to evaluate the leachate toxicity of Cr(VI). The effects of the initial soil Cr(VI) concentration, montmorillonites dosage, reaction time and HDTMA modification amount were investigated, respectively. The results revealed that modification of montmorillonites would manifest an attenuated physical adsorptive effect and an enhanced electrostatic adsorptive effect on Cr(VI), suggesting electrostatic effect was the major force that resulted in improved Cr(VI) adsorption onto HDTMA modified montmorillonites. PMID:27337898

  13. Surface characterization of plasma-treated polypropylene fibers

    SciTech Connect

    Wei, Q.F

    2004-06-15

    Plasma treatment is increasingly being used for surface modification of different materials in many industries. In this study, different techniques were employed to characterize the surface properties of plasma treated polypropylene fibers. The chemical nature of the fiber sufaces has been investigated by X-ray photoelectron spectroscopy (XPS). The XPS examination indicated the presence of oxygen-containing functional groups on fiber surfaces after plasma treatment. The Atomic Force Microscopy (AFM) scans revealed the evolution of surface morphology under different experimental conditions. A Philips Environmental Scanning Electron Microscopy (ESEM) was also used to study the wetting behavior of the fibers. In the ESEM, relative humidity can be raised to 100% to facilitate the water condensation onto fiber surfaces for wetting observation. The ESEM observation revealed that the plasma treatment significantly altered the surface wettability of polypropylene fibers.

  14. Utilization of surface-treated rubber particles from waste tires

    SciTech Connect

    Smith, F.G. |

    1994-12-01

    During a 12-month program, the author successfully demonstrated commercial applications for surface-treated rubber particles in two major markets: footwear (shoe soles and components) and urethane-foam carpet underlay (padding). In these markets, he has clearly demonstrated the ease of using R-4080 and R-4030 surface-treated rubber particles in existing manufacturing plants and processes and have shown that the material meets or exceeds existing standards for performance, quality, and cost-effectiveness. To produce R-4080 and R-4030, vulcanized rubber, whole-tire material is finely ground to particles of nominal 80 and mesh size respectively. Surface treatment is achieved by reacting these rubber particles with chlorine gas. In this report, the author describes the actual test and evaluations of the participant companies, and identifies other potential end uses.

  15. Biodegradable nanocomposites from toughened polyhydroxybutyrate and titanate-modified montmorillonite clay

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Montmorillonite clay treated with neopentyl (diallyl)oxy tri( dioctyl) pyrophosphato-titanate was used as a reinforcement for toughened bacterial bioplastic, Polyhydroxybutyrate (PHB) in order to develop novel biodegradable nanocomposites. The modified clay, PHB, toughening partner and specific comp...

  16. Induced hydrophobic recovery of oxygen plasma-treated surfaces

    PubMed Central

    Guckenberger, David J.; Berthier, Erwin; Young, Edmond W. K.; Beebe, David J.

    2014-01-01

    Plasma treatment is a widely used method in microfabrication laboratories and the plasticware industry to functionalize surfaces for device bonding and preparation for mammalian cell culture. However, spatial control of plasma treatment is challenging because it typically requires a tedious masking step that is prone to alignment errors. Currently, there are no available methods to actively revert a surface from a treated hydrophilic state to its original hydrophobic state. Here, we describe a method that relies on physical contact treatment (PCT) to actively induce hydrophobic recovery of plasma-treated surfaces. PCT involves applying brushing and peeling processes with common wipers and tapes to reverse the wettability of hydrophilized surfaces while simultaneously preserving hydrophilicity of non-contacted surfaces. We demonstrate that PCT is a user-friendly method that allows 2D and 3D surface patterning of hydrophobic regions, and the protection of hydrophilic surfaces from unwanted PCT-induced recovery. This method will be useful in academic and industrial settings where plasma treatment is frequently used. PMID:22592853

  17. Preparation and characterization of zwitterionic surfactant-modified montmorillonites.

    PubMed

    Zhu, Jianxi; Qing, Yanhong; Wang, Tong; Zhu, Runliang; Wei, Jingming; Tao, Qi; Yuan, Peng; He, Hongping

    2011-08-15

    A series of zwitterionic surfactant-modified montmorillonites (ZSMMs) were synthesized using montmorillonite and three zwitterionic surfactants with different alkyl chain lengths at different concentrations [0.2-4.0 cation exchange capacity (CEC)]. These ZSMMs were characterized by X-ray diffraction (XRD), thermo-gravimetric analysis and differential thermo-gravimetric (TG/DTG) analyses. The zwitterionic surfactant could be intercalated into the interlayer spaces of montmorillonites and causing interlayer space-swelling. From XRD measurements, the amount of the surfactants loaded and the basal spacing increased with surfactant concentration and alkyl chain length. One endothermic DTG peak occurred at ~390 °C, which was assigned to the decomposition of the zwitterionic surfactant on the organo-montmorillonites from 0.2 to 0.6 CEC. When the surfactant loading was increased, a new endothermic peak appeared at ~340 °C. From the microstructures of these ZSMMs, the mechanism of zwitterionic surfactant adsorption was proposed. At relatively low loadings of the zwitterionic surfactant, most of surfactants enter the spacing by an ion-exchange mechanism and are adsorbed onto the interlayer cation sites. When the concentration of the zwitterionic surfactant exceeds the CEC of montmorillonite, the surfactant molecules then adhere to the surface-adsorbed surfactant. Some surfactants enter the interlayers, whereas the others are attached to the clay surface. When the concentration of surfactant increases further beyond 2.0 CEC, the surfactants may occupy the inter-particle space within the house-of-cards aggregate structure. PMID:21575956

  18. Adsorption of ammonia on treated stainless steel and polymer surfaces

    NASA Astrophysics Data System (ADS)

    Vaittinen, O.; Metsälä, M.; Persijn, S.; Vainio, M.; Halonen, L.

    2014-05-01

    Adsorption of dynamically diluted ammonia at part-per-billion to low part-per-million concentrations in dry nitrogen was studied with treated and non-treated stainless steel and polymer test tubes. The treatments included electropolishing and two types of coatings based on amorphous silicon. Cavity ring-down spectroscopy with an external cavity diode laser operating in the near-infrared wavelength range was used to monitor the adsorption process in real time in continuous-flow conditions to obtain quantitative assessment of the adsorptive properties of the studied surfaces. The investigated polymers were all less adsorptive than any of the treated or non-treated stainless steel surfaces. Some of the commercial coatings reduced the adsorption loss of stainless steel by a factor of ten or more. Polyvinylidene fluoride was found to be superior (less adsorption) to the four other studied polymer coatings. The number of adsorbed ammonia molecules per surface area obtained at different ammonia gas phase concentrations was modeled with Langmuir and Freundlich isotherms. The time behavior of the adsorption-desorption process occurring in the time scale of seconds and minutes was simulated with a simple kinetic model.

  19. Stability of plasma treated superhydrophobic surfaces under different ambient conditions.

    PubMed

    Chen, Faze; Liu, Jiyu; Cui, Yao; Huang, Shuai; Song, Jinlong; Sun, Jing; Xu, Wenji; Liu, Xin

    2016-05-15

    Plasma hydrophilizing of superhydrophobic substrates has become an important area of research, for example, superhydrophobic-(super)hydrophilic patterned surfaces have significant practical applications such as lab-on-chip systems, cell adhesion, and control of liquid transport. However, the stability of plasma-induced hydrophilicity is always considered as a key issue since the wettability tends to revert back to the untreated state (i.e. aging behavior). This paper focuses on the stability of plasma treated superhydrophobic surface under different ambient conditions (e.g. temperature and relative humidity). Water contact angle measurement and X-ray photoelectron spectroscopy are used to monitor the aging process. Results show that low temperature and low relative humidity are favorable to retard the aging process and that pre-storage at low temperature (-10°C) disables the treated surface to recover superhydrophobicity. When the aging is performed in water, a long-lasting hydropholicity is obtained. As the stability of plasma-induced hydrophilcity over a desired period of time is a very important issue, this work will contribute to the optimization of storage conditions of plasma treated superhydrophobic surfaces. PMID:26945118

  20. Treating ocular surface disease: new agents in development

    PubMed Central

    Fahmy, Ahmad M; Hardten, David R

    2011-01-01

    This paper reviews recent advances and investigation in the treatment of ocular surface pathology. There is significant investment in this area, paralleling the growing demand for more effective alternatives to current treatments. Clinicians are becoming more aware of surface pathology, yet the ability to treat the most common forms of ocular pathology are still limited to the few medications approved by the US Food and Drug Administration. Medicines and devices currently under investigation are very promising. It is absolutely critical to understand the emerging options and think of their role in the treatment paradigm. PMID:21573093

  1. Surface characterization of silica glass substrates treated by atomic hydrogen

    SciTech Connect

    Inoue, Hiroyuki; Masuno, Atsunobu; Ishibashi, Keiji; Tawarayama, Hiromasa; Zhang, Yingjiu; Utsuno, Futoshi; Koya, Kazuo; Fujinoki, Akira; Kawazoe, Hiroshi

    2013-12-15

    Silica glass substrates with very flat surfaces were exposed to atomic hydrogen at different temperatures and durations. An atomic force microscope was used to measure root-mean-square (RMS) roughness and two-dimensional power spectral density (PSD). In the treatment with atomic hydrogen up to 900 °C, there was no significant change in the surface. By the treatment at 1000 °C, the changes in the RMS roughness and the PSD curves were observed. It was suggested that these changes were caused by etching due to reactions of atomic hydrogen with surface silica. By analysis based on the k-correlation model, it was found that the spatial frequency of the asperities became higher with an increase of the treatment time. Furthermore, the data showed that atomic hydrogen can flatten silica glass surfaces by controlling heat-treatment conditions. - Highlights: • Silica glass surface was treated by atomic hydrogen at various temperatures. • Surface roughness was measured by an atomic force microscope. • Roughness data were analyzed by two-dimensional power spectral density. • Atomic hydrogen can flatten silica glass surfaces.

  2. Alkylammonium montmorillonites as adsorbents for organic vapors from air

    SciTech Connect

    Harper, M.; Purnell, C.J. )

    1990-01-01

    Montmorillonite clays may be modified by the exchange of the inorganic interlayer cations with alkylammonium ions, resulting in a fixed internal porosity. The pore size and shape depend on the nature of the alkylammonium ion. A number of different ions were used to prepare adsorbents with varying properties, and these were examined for their potential application to sampling organic vapors in air. Characterization involved determination of nitrogen and water contents, surface area, interlayer spacing, thermal stability, and breakthrough volumes of organic vapors. The adsorbent that showed the most promise (tetramethylammonium montmorillonite (TMA)) was further evaluated for use as an adsorbent in both thermal- and solvent-desorable sampling systems.

  3. Flame retardant polypropylene nanocomposites reinforced with surface treated carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Guleria, Abhishant

    Polypropylene nanocomposites are prepared by reinforcing carbon nanotubes by ex-situ solution mixing method. Interfacial dispersion of carbon nanotubes in polypropylene have been improved by surface modification of CNTs and adding surfactants. Polypropylene nanocomposites fabrication was done after treating CNTs. Firstly, oxidation of CNTs followed by silanization for addition of functionalized groups on the surface of CNTs. Maleic anhydride grafted PPs were used as surfactants. Maleic anhydrides with two different molecular weights were LAMPP and HMAPP. Successful oxidation of CNTs by nitric acid and functionalized CNTs by 3-Aminopropyltriethoxysilane was confirmed by attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) with evidence of absorption peak at 1700 and 1100-1000 cm-1. Scanning electron microscopy (SEM) micrographs revealed that the CNTs dispersion quality was improved by directly adding LMAPP/HMAPP into PP/CNTs system and the PP-CNTs adhesion was enhanced through both the CNTs surface treatment and the addition of surfactant. Thermal gravimetric analysis (TGA) revealed an enhanced thermal stability in the PP/CNTs and PP/CNTs/MAPP. Differential scanning calorimetry (DSC) characterization demonstrated that the crystalline temperature, fusion heat and crystalline fraction of hosting PP were decreased with the introduction of CNTs and surface treated CNTs; however, melting temperature was only slightly changed. Melting rheological behaviors including complex viscosity, storage modulus, and loss modulus indicated significant changes in the PP/MAPP/CNTs system before and after functionalization of CNTs, and the mechanism were also discussed in details.

  4. The mechanism of montmorillonite catalysis in RNA synthesis

    NASA Astrophysics Data System (ADS)

    Joshi, Prakash

    montmorillonite as reaction occurs. The application of the Scherer equation to the X-ray diffraction data showed differences in domain size. Modeling of the size of the activated nucleotide monomers and the charge on the montmorillonite surface provided an interpretation of how these factors influence adsorption. This research provides a basis for further understanding of the physical processes in the mechanism of this catalysis in prebiotic reactions. This research was supported by NASA Astrobiology Institute Grant NNA09DA80A. References: Aldersley, M.F., Joshi, P.C., Price, J.D., Ferris, J.P. The role of montmorillonite in its catalysis of RNA synthesis. Appl. Clay Sci. 54,1-14, 2011. Bishop, J.L., Dobrea, E.J.N., Mckeown, N.K., Parenta, M. Phyllos- ilicate diversity and past aqueous activity revealed at Mawrth Vallis, Mars. Science 321, 830-833, 2008. Joshi, P.C., Aldersley, M.F., Delano, J.W., Ferris, J.P., Mechanism of montmorillonite catalysis in the formation of RNA oligomers, J. Am. Chem. Soc., 131, 13369-13374, 2009.

  5. Montmorillonite-Alginate Composites as a Drug delivery System: Intercalation and In vitro Release of Diclofenac sodium

    PubMed Central

    Kevadiya, B. D.; Patel, H. A.; Joshi, G. V.; Abdi, S. H. R.; Bajaj, H. C.

    2010-01-01

    Diclofenac sodium and alginate was intercalated into montmorillonite to form uniform sized beads by gelation method. The structure and surface morphology of the synthesized composite beads were characterized by powdered X-ray diffraction, Fourier transform infrared spectroscopy, thermo gravimetric analysis and scanning electron microscopy. Diclofenac release kinetics of the composite in simulated intestinal fluid medium (pH 7.4) and effect of montmorillonite content on the in vitro release of diclofenac from diclofenac-montmorillonite-alginate composites bead was investigated by UV/Vis spectrophotometer. Diclofenac encapsulation efficiency in the montmorillonite-alginate composites bead increases with an increase in the montmorillonite content. The control release of diclofenac from diclofenac-montmorillonite-alginate composites beads was observed to be better as compared to diclofenac-alginate beads. PMID:21969745

  6. Surface energy increase of oxygen-plasma-treated PET

    SciTech Connect

    Cioffi, M.O.H.; Voorwald, H.J.C.; Mota, R.P

    2003-03-15

    Prosthetic composite is a widely used biomaterial that satisfies the criteria for application as an organic implant without adverse reactions. Polyethylene therephthalate (PET) fiber-reinforced composites have been used because of the excellent cell adhesion, biodegradability and biocompatibility. The chemical inertness and low surface energy of PET in general are associated with inadequate bonds for polymer reinforcements. It is recognized that the high strength of composites, which results from the interaction between the constituents, is directly related to the interfacial condition or to the interphase. A radio frequency plasma reactor using oxygen was used to treat PET fibers for 5, 20, 30 and 100 s. The treatment conditions were 13.56 MHz, 50 W, 40 Pa and 3.33x10{sup -7} m{sup 3}/s. A Rame-Hart goniometer was used to measure the contact angle and surface energy variation of fibers treated for different times. The experimental results showed contact angle values from 47 deg. to 13 deg. and surface energies from 6.4x10{sup -6} to 8.3x10{sup -6} J for the range of 5 to 100 s, respectively. These results were confirmed by the average ultimate tensile strength of the PET fiber/ polymethylmethacrylate (PMMA) matrix composite tested in tensile mode and by scanning electron microscopy.

  7. Molecular dynamics simulation of the intercalation behaviors of methane hydrate in montmorillonite.

    PubMed

    Yan, KeFeng; Li, XiaoSen; Xu, ChunGang; Lv, QiuNan; Ruan, XuKe

    2014-06-01

    The formation and mechanism of CH4 hydrate intercalated in montmorillonite are investigated by molecular dynamics (MD) simulation. The formation process of CH4 hydrate in montmorillonite with 1 ~ 8 H2O layers is observed. In the montmorillonite, the "surface H2O" constructs the network by hydrogen bonds with the surface Si-O ring of clay, forming the surface cage. The "interlayer H2O" constructs the network by hydrogen bonds, forming the interlayer cage. CH4 molecules and their surrounding H2O molecules form clathrate hydrates. The cation of montmorillonite has a steric effect on constructing the network and destroying the balance of hydrogen bonds between the H2O molecules, distorting the cage of hydrate in clay. Therefore, the cages are irregular, which is unlike the ideal CH4 clathrate hydrates cage. The pore size of montmorillonite is another impact factor to the hydrate formation. It is quite easier to form CH4 hydrate nucleation in montmorillonite with large pore size than in montmorillonite with small pore. The MD work provides the constructive information to the investigation of the reservoir formation for natural gas hydrate (NGH) in sediments. PMID:24906646

  8. Transformation of montmorillonite to kaolinite during weathering

    USGS Publications Warehouse

    Altschuler, Z.S.; Dwornik, E.J.; Kramer, H.

    1963-01-01

    Extensive deposits of kaolinite in Florida are formed by transformation of montmorillonite during low-temperature supergene weathering. The transformation occurs by intracrystalline leaching of interlayer cations and tetrahedral silica layers. Interposition of stripped layers within montmorillonite creates a regular 1:1 mixed-layered montmorillonite-kaolinite, a new clay structure. Kaolin-like layers are nourished by lateral epitaxy, as the iron-rich montmorillonite decomposes. Hexagonal outgrowths of new kaolinite develop at the edges of montmorillonite flakes and nucleate new vertical growth. Kaolinitic sands impregnated with goethite are ultimately formed, and the released silica enriches groundwater and forms secondary chert.

  9. The adsorption and reaction of adenine nucleotides on montmorillonite.

    PubMed

    Ferris, J P; Hagan, W J

    1986-01-01

    The binding of AMP to Zn(2+)-montmorillonite was investigated in the presence of buffers and salts. Good's buffers, piperazine-N,N'-bis(2-ethanesulfonate) [PIPES] and morpholine-N-2-ethanesulfonate [MES], perturbed the exchangeable cations to a lesser extent (only 9% of Zn2+ displaced by 0.2 M buffer) than was observed with imidazole and lutidine buffers or NaCl and KCl salts (up to 80% of Zn2+ displaced). AMP adsorption isotherms measured in the presence of 0.2 M PIPES, MES, or Na2SO4 exhibited normal Langmuir-type behavior. The adsorption coefficient, KL, is 3-fold greater in the presence of HEPES or PIPES than it is in the absence of buffers. Basal spacings measured by X-ray diffraction for Zn(2+)-montmorillonite are 13 and 15 angstroms in the presence of PIPES, while a value of 12.8 angstroms was determined in the absence of PIPES. These data are interpreted in a model in which the adsorption of AMP is mediated by a Zn2+ complex of PIPES in different orientations in the interlamellar region of the montmorillonite. The type of exchangeable cation does not affect the ability of the lattice-bound Fe3+ in the montmorillonite to oxidize diaminomaleonitrile (DAMN). Exchangeable Cu2+ oxidizes DAMN, but exchangeable Fe3+ is nearly ineffective as an oxidant. The addition of DISN to 3'-AMP bound to Zn(2+)-montmorillonite in the presence of 0.2 M PIPES resulted in a higher yield of 2',3'-cAMP than is observed with a comparable concentration of Zn2+, a result which inplicates surface catalysis by the montmorillonite. PMID:11540864

  10. Sorption of sodium dodecylbenzene sulfonate by montmorillonite.

    PubMed

    Yang, Kun; Zhu, Lizhong; Xing, Baoshan

    2007-01-01

    Sorption of linear alkylbenzene sulfonates by soils and sediments is an important process that may affect their fate, transport, toxicity and their application in remediation of contaminated soil and groundwater. In this study, batch experiments were conducted to elucidate the sorption of a widely used anionic surfactant, sodium dodecylbenzene sulfonate (SDBS), by montmorillonite. It was observed that: (i) SDBS was sorbed significantly by montmorillonite saturated with Ca(2+), but little by Na-saturated montmorillonite; (ii) the amount of SDBS sorbed by Ca(2+)-montmorillonite was enhanced by NaCl; and (iii) no significant intercalation of SDBS into Ca(2+)-montmorillonite was observed by X-ray diffraction (XRD) analysis. These results indicate that the removal of SDBS by Ca(2+)-montmorillonite was primarily attributed to the precipitation between DBS(-) and Ca(2+) in solution which was released from montmorillonite via cation exchange. These results will help us to understand the sorption behavior and environmental effects of anionic surfactants. PMID:16759775

  11. Development of Surface Complexation Models of Cr(VI) Adsorption on Soils, Sediments and Model Mixtures of Kaolinite, Montmorillonite, γ-Alumina, Hydrous Manganese and Ferric Oxides and Goethite

    SciTech Connect

    Koretsky, Carla

    2013-11-29

    Hexavalent chromium is a highly toxic contaminant that has been introduced into aquifers and shallow sediments and soils via many anthropogenic activities. Hexavalent chromium contamination is a problem or potential problem in the shallow subsurface at several DOE sites, including Hanford, Idaho National Laboratory, Los Alamos National Laboratory and the Oak Ridge Reservation (DOE, 2008). To accurately quantify the fate and transport of hexavalent chromium at DOE and other contaminated sites, robust geochemical models, capable of correctly predicting changes in chromium chemical form resulting from chemical reactions occurring in subsurface environments are needed. One important chemical reaction that may greatly impact the bioavailability and mobility of hexavalent chromium in the subsurface is chemical binding to the surfaces of particulates, termed adsorption or surface complexation. Quantitative thermodynamic surface complexation models have been derived that can correctly calculate hexavalent chromium adsorption on well-characterized materials over ranges in subsurface conditions, such pH and salinity. However, models have not yet been developed for hexavalent chromium adsorption on many important constituents of natural soils and sediments, such as clay minerals. Furthermore, most of the existing thermodynamic models have been developed for relatively simple, single solid systems and have rarely been tested for the complex mixtures of solids present in real sediments and soils. In this study, the adsorption of hexavalent chromium was measured as a function of pH (3-10), salinity (0.001 to 0.1 M NaNO3), and partial pressure of carbon dioxide(0-5%) on a suite of naturally-occurring solids including goethite (FeOOH), hydrous manganese oxide (MnOOH), hydrous ferric oxide (Fe(OH)3), γ-alumina (Al2O3), kaolinite (Al2Si2O5(OH)4), and montmorillonite (Na3(Al, Mg)2Si4O10(OH)2-nH2O). The results show that all of these materials can bind substantial quantities of

  12. Electrolyte diffusion in compacted montmorillonite engineered barriers

    SciTech Connect

    Jahnke, F.M.; Radke, C.J.

    1985-09-01

    The bentonite-based engineered barrier or packing is a proposed component of several designs conceived to dispose of high-level nuclear waste in geologic repositories. Once radionuclides escape the waste package, they must first diffuse through the highly impermeable clay-rich barrier before they reach the host repository. To determine the effectiveness of the packing as a sorption barrier in the transient release period and as a mass-transfer barrier in the steady release period over the geologic time scales involved in nuclear waste disposal, a fundamental understanding of the diffusion of electrolytes in compacted clays is required. We present, and compare with laboratory data, a model quantifying the diffusion rates of cationic cesium and uncharged tritium in compacted montmorillonite clay. Neutral tritium characterizes the geometry (i.e., tortuosity) of the particulate gel. After accounting for cation exchange, we find that surface diffusion is the dominant mechanism of cation transport, with an approximate surface diffusion coefficient of 2 x 10 W cmS/s for cesium. This value increases slightly with increasing background ionic strength. The implications of this work for the packing as a migration barrier are twofold. During the transient release period, K/sub d/ values are of little importance in retarding ion migration. This is because sorption also gives rise to a surface diffusion path, and it is surface diffusion which controls the diffusion rate of highly sorbing cations in compacted montmorillonite. During the steady release period, the presence of surface diffusion leads to a flux through the packing which is greatly enhanced. In either case, if surface diffusion is neglected, the appropriate diffusion coefficient of ions in compacted packing will be in considerable error relative to current design recommendations. 11 refs., 4 figs., 1 tab.

  13. Cotransport of bismerthiazol and montmorillonite colloids in saturated porous media

    NASA Astrophysics Data System (ADS)

    Shen, Chongyang; Wang, Hong; Lazouskaya, Volha; Du, Yichun; Lu, Weilan; Wu, Junxue; Zhang, Hongyan; Huang, Yuanfang

    2015-06-01

    While bismerthiazol [N,N‧-methylene-bis-(2-amino-5-mercapto-1,3,4-thiadiazole)] is one of the most widely used bactericides, the transport of bismerthiazol in subsurface environments is unclear to date. Moreover, natural colloids are ubiquitous in the subsurface environments. The cotransport of bismerthiazol and natural colloids has not been investigated. This study conducted laboratory column experiments to examine the transport of bismerthiazol in saturated sand porous media both in the absence and presence of montmorillonite colloids. Results show that a fraction of bismerthiazol was retained in sand and the retention was higher at pH 7 than at pH 4 and 10. The retention did not change with ionic strength. The retention was attributed to the complex of bismerthiazol with metals/metal oxides on sand surfaces through ligand exchange. The transport of bismerthiazol was enhanced with montmorillonite colloids copresent in the solutions and, concurrently, the transport of montmorillonite colloids was facilitated by the bismerthiazol. The transport of montmorillonite colloids was enhanced likely because the bismerthiazol and the colloids competed for the attachment/adsorption sites on collector surfaces and the presence of bismerthiazol changed the Derjaguin-Landau-Verwey-Overbeek (DLVO) interaction energies between colloids and collectors. The transport of bismerthiazol was inhibited if montmorillonite colloids were pre-deposited in sand because bismerthiazol could adsorb onto the colloid surfaces. The adsorbed bismerthiazol could be co-remobilized with the colloids from primary minima by decreasing ionic strength. Whereas colloid-facilitated transport of pesticides has been emphasized, our study implies that transport of colloids could also be facilitated by the presence of pesticides.

  14. Surface analysis of polymers treated by remote atmospheric pressure plasma.

    PubMed

    Gonzalez, Eleazar; Hicks, Robert F

    2010-03-01

    The surfaces of high-density polyethylene (HDPE), poly(methyl methacrylate) (PMMA), and polyethersulfone (PES) were treated with a low-temperature, atmospheric pressure oxygen and helium plasma. The polymers were exposed to the downstream afterglow of the plasma, which contained primarily oxygen atoms and metastable oxygen molecules ((1)Delta(g) O(2)), and no ions or electrons. X-ray photoelectron spectroscopy (XPS) of HDPE revealed that 20% of the carbon atoms were converted into oxidized functional groups, with about half of these being carboxylic acids. Attenuated total reflection infrared spectroscopy of all three polymers was obtained in order to determine the types of functional groups formed by atmospheric plasma exposure. It was found that the polymers were rapidly oxidized with addition of alcohols, ketones, and carboxylic acids to the carbon backbone. Chain scission occurred on HDPE and PMMA, while on PES the aromatic groups underwent ring-opening and insertion of carboxylic acid. PMID:19950952

  15. Montmorillonite enhanced ciprofloxacin transport in saturated porous media with sorbed ciprofloxacin showing antibiotic activity

    NASA Astrophysics Data System (ADS)

    Chen, Hao; Gao, Bin; Yang, Liu-Yan; Ma, Lena Q.

    2015-02-01

    Antibiotic ciprofloxacin (CIP) is immobile in the subsurface but it has been frequently detected in the aquatic system. Therefore it is important to investigate the factors impacting CIP's mobilization in aquifer. Laboratory columns packed with sand were used to test colloid-facilitated CIP transport by 1) using kaolinite or montmorillonite to mobilize presorbed-CIP in a column or 2) co-transporting with CIP by pre-mixing them before transport. The Langmuir model showed that CIP sorption by montmorillonite (23 g kg- 1) was 100 times more effective than sand or kaolinite. Even with strong CIP complexation ability to Fe/Al coating on sand surface, montmorillonite promoted CIP transport, but not kaolinite. All presorbed-CIP by sand was mobilized by montmorillonite after 3 pore volumes through co-transporting of CIP with montmorillonite. The majority of CIP was fixed onto the montmorillonite interlayer but still showed inhibition of bacteria growth. Our results suggested that montmorillonite with high CIP sorption ability can act as a carrier to enhance CIP's mobility in aquifer.

  16. Laser-ultrasonic surface wave dispersion measurements on surface-treated metals.

    PubMed

    Ruiz, Alberto; Nagy, Peter B

    2004-04-01

    Surface acoustic wave (SAW) velocity spectroscopy has been long considered to be one of the leading candidates for nondestructive characterization of surface-treated metals because of its ability to probe the material properties at different penetration depths depending on the inspection frequency. We developed a high-precision laser-ultrasonic technique to study the feasibility of SAW dispersion spectroscopy for residual stress assessment on shot-peened metals. This technique is capable of measuring SAW dispersion with a relative error of 0.1% over a frequency range from 2 to 15 MHz. Our experimental results obtained from shot-peened aluminum 2024-T351 samples indicate that the dispersion of the surface wave is a superposition of different effects of surface treatment in the material, including surface roughness, compressive residual stress, and cold work. Although the surface roughness induced component is often the dominating part of the overall dispersion, the experimental results also indicate that it is feasible to observe a perceivable change in the dispersion of the SAW when the specimen is heat-treated at different temperatures, which has no perceivable effect on the surface roughness. The part of the dispersion, which changes during annealing via thermal relaxation, is due to near-surface residual stresses and the decay of texture, although at high frequencies nonuniform grain coarsening could also play a significant role. PMID:15047364

  17. Chitosan-Montmorillonite microspheres: A sustainable fertilizer delivery system.

    PubMed

    dos Santos, Bruna Rodrigues; Bacalhau, Fabiana Britti; Pereira, Tamires dos Santos; Souza, Claudinei Fonseca; Faez, Roselena

    2015-08-20

    Controlled release fertilizers are efficient tools that increase the sustainability of agricultural practices. However, the biodegradability of the matrices and the determination of the release into soil still require some investigation. This paper describes the preparation of potassium-containing microspheres based on chitosan and montmorillonite clay and the in situ soil release. The chitosan-montmorillonite microspheres were prepared using a coagulation method and different proportions of montmorillonite. The structural, thermal and morphological properties as well the water swelling and fertilizer sorption capacity were evaluated. The best formulations were applied in soil, and the fertilizer release was monitored using time-domain reflectometry (TDR). Montmorillonite clay provides better sorption properties than the chitosan microspheres because of the rough and porous surface. Due to these properties, high levels of fertilizer were sorbed onto the material. ChMMT33-containing potassium shows two specific periods of fertilizer release: the first one lasted approximately three days and was assigned to the external fertilizer on the microspheres. The second was assigned to the internal fertilizer. TDR is an important and fast tool and was used to determine the fertilizer release and the ion movement in the soil. PMID:25965492

  18. 40 CFR 721.10222 - Styrenyl surface treated manganese ferrite (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Styrenyl surface treated manganese... Specific Chemical Substances § 721.10222 Styrenyl surface treated manganese ferrite (generic). (a) Chemical... as styrenyl surface treated manganese ferrite (PMN P-09-581) is subject to reporting under...

  19. 40 CFR 721.10222 - Styrenyl surface treated manganese ferrite (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Styrenyl surface treated manganese... Specific Chemical Substances § 721.10222 Styrenyl surface treated manganese ferrite (generic). (a) Chemical... as styrenyl surface treated manganese ferrite (PMN P-09-581) is subject to reporting under...

  20. 40 CFR 721.10222 - Styrenyl surface treated manganese ferrite (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Styrenyl surface treated manganese... Specific Chemical Substances § 721.10222 Styrenyl surface treated manganese ferrite (generic). (a) Chemical... as styrenyl surface treated manganese ferrite (PMN P-09-581) is subject to reporting under...

  1. Comparison of removal torques between laser-treated and SLA-treated implant surfaces in rabbit tibiae

    PubMed Central

    Kang, Nam-Seok; Li, Lin-Jie

    2014-01-01

    PURPOSE The purpose of this study was to compare removal torques and surface topography between laser treated and sandblasted, large-grit, acid-etched (SLA) treated implants. MATERIALS AND METHODS Laser-treated implants (experimental group) and SLA-treated implants (control group) 8 mm in length and 3.4 mm in diameter were inserted into both sides of the tibiae of 12 rabbits. Surface analysis was accomplished using a field emission scanning electron microscope (FE-SEM; Hitachi S-4800; Japan) under ×25, ×150 and ×1,000 magnification. Surface components were analyzed using energy dispersive spectroscopy (EDS). Rabbits were sacrificed after a 6-week healing period. The removal torque was measured using the MGT-12 digital torque meter (Mark-10 Co., Copiague, NY, USA). RESULTS In the experimental group, the surface analysis showed uniform porous structures under ×25, ×150 and ×1,000 magnification. Pore sizes in the experimental group were 20-40 mm and consisted of numerous small pores, whereas pore sizes in the control group were 0.5-2.0 mm. EDS analysis showed no significant difference between the two groups. The mean removal torque in the laser-treated and the SLA-treated implant groups were 79.4 Ncm (SD = 20.4; range 34.6-104.3 Ncm) and 52.7 Ncm (SD = 17.2; range 18.7-73.8 Ncm), respectively. The removal torque in the laser-treated surface implant group was significantly higher than that in the control group (P=.004). CONCLUSION In this study, removal torque values were significantly higher for laser-treated surface implants than for SLA-treated surface implants. PMID:25177474

  2. Exfoliation and intercalation of montmorillonite by small peptides

    PubMed Central

    Block, Karin A.; Trusiak, Adrianna; Katz, Al; Alimova, Alexandra; Wei, Hui; Gottlieb, Paul; Steiner, Jeffrey C.

    2015-01-01

    Understanding structural changes in clay minerals induced by complexation with organic matter is relevant to soil science and agricultural applications. In this study, the effect of peptide storage in montmorillonite and the thermal stability of peptide-clay complexes was examined through characterization by X-ray diffraction (XRD), electron microscopy, UV absorption, and thermogravimetric analysis (TGA). XRD analysis of small peptide-montmorillonite clay complexes produced profiles consisting of reflections associated with the smectite 001 reflection and related peaks similar to that produced by a mixed layer clay mineral structure. Shifts in higher order diffraction maxima were attributed to disorder caused by the intercalation with the peptides. Increasing peptide concentrations resulted in greater shifts towards smaller 2θ from 6.37° (1.39 nm) to 5.45° (1.62 nm) as the interlayer space expanded. The expansion was accompanied by broadening of the 001 reflection (FWHM increases from 0.51 to 1.22° 2θ). The XRD line broadening was interpreted as caused by poorer crystallinity resulting from intercalation and tactoid exfoliation. SEM images revealed montmorillonite platelets with upwardly rolled edges that tend toward cylindrical structures with the production of tubules. High-resolution TEM images revealed bending of montmorillonite platelets, confirming exfoliation. The distribution of basal spacings in the micrographs was determined from the spatial frequencies obtained by Fourier analysis of density profiles. The distribution indicated the presence of discrete coherent crystallite domains. XRD and TGA results indicated that higher peptide concentrations resulted in a greater fraction of intercalated peptides and that surface adsorption of peptides mediated intercalation. Therefore, higher peptide concentration led to more stable organoclay complexes. However, UV absorption and TGA found that peptide adsorption onto montmorillonite had a finite limit at

  3. Method and system for treating an interior surface of a workpiece using a charged particle beam

    DOEpatents

    Swenson, David Richard

    2007-05-23

    A method and system of treating an interior surface on an internal cavity of a workpiece using a charged particle beam. A beam deflector surface of a beam deflector is placed within the internal cavity of the workpiece and is used to redirect the charged particle beam toward the interior surface to treat the interior surface.

  4. Structural properties of reduced Upton montmorillonite

    NASA Astrophysics Data System (ADS)

    Gates, W. P.; Stucki, J. W.; Kirkpatrick, R. J.

    1996-12-01

    Reduction of octahedral Fe in the crystalline structure of smectites influences, possibly controls, surface-sensitive physical and chemical properties. The purpose of this study was to investigate if reduction of structural Fe by Na-dithionite or bacteria affects the chemical environment of constituent cations in montmorillonite, employing solid state multinuclear (29Si and 27Al) magic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy. Reduction of structural Fe resulted in a positive (down field) chemical shift of the main Si Q3 (Q3(0Al)) site which was strongly correlated with Fe(II) content and inferred that distortions in Si-OT (T=Si, Al) bond angles and Si-O bond lengths occur with increasing layer charge. The line width (W) of the 29Si Q3 signal also increased with increasing levels of reduction. No change occurred in the position of the peak maximum for the octahedral Al (27AlVI) signal; however, an increased W was observed for this peak with increasing Fe(II) content. These results are attributed to decreases in Si-O-T bond angles and Si-O bond distances, corresponding to a better fit between the tetrahedral and octahedral sheets brought about by the presence of Fe(II) in the clay structure. The increased 27AlVI signal width (W) may also be due to a lessening of the paramagnetic influence of Fe(III) nuclei and enhancement of 27AlVI signals with different quadrupole coupling constants (QCC). Multinuclear MAS NMR analyses of dithioniteand microbially-reduced montmorillonite indicate that reduction of structural Fe caused reversible changes in the smectite structure, at least as far as this method could discern.

  5. Controllable surface morphology and properties via mist polymerization on a plasma-treated polymethyl methacrylate surface.

    PubMed

    Wan, S J; Wang, L; Xu, X J; Zhao, C H; Liu, X D

    2014-02-14

    Surface modification by grafting polymers on solid materials is an important strategy used to improve surface properties. This article reports that under appropriate conditions, very thin layers with desired morphologies may be constructed on a plasma-treated substrate by feeding a small quantity of a monomer with a mist stream carrying droplets produced from monomer solutions. We investigate the effects of process parameters that affect layer morphology, including exposure time to the mist stream, concentration of the monomer solution, and solvent selectivity. For a methyl methacrylate solution in ethanol, nanoparticles are uniformly grown with increasing monomer concentration or exposure time and finally form a porous layer at 3.65 mol L(-1) for 30 min. Decreasing solvent polarity not only affects surface morphology, but also increases hydrophobicity of the resulting surface. With 2,2,3,4,4,4-hexafluorobutyl methacrylate as the monomer, SEM and AFM micrographs indicated that mist polymerization results in numerous microspheres on the activated surface. These experimental results were interpreted by a mechanism in terms of an in situ polymerization accompanied by a phase transformation of the resulting polymer. Specifically, plasma treatment provides highly active cations and radicals to initiate very rapid polymerization, and the resulting polymers are consequently deposited from the liquid onto the surface under phase transition mechanisms. PMID:24835436

  6. 40 CFR 721.10223 - Styrenyl surface treated manganese ferrite with acrylic ester polymer (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Styrenyl surface treated manganese... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10223 Styrenyl surface treated... subject to reporting. (1) The chemical substance identified generically as styrenyl surface...

  7. 40 CFR 721.10223 - Styrenyl surface treated manganese ferrite with acrylic ester polymer (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Styrenyl surface treated manganese... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10223 Styrenyl surface treated... subject to reporting. (1) The chemical substance identified generically as styrenyl surface...

  8. Influence of the organic complex concentration on adsorption of herbicide in organic modified montmorillonite

    NASA Astrophysics Data System (ADS)

    Kaludjerovic, Lazar; Tomic, Zorica; Djurovic, Rada; Milosevic, Maja

    2016-04-01

    Pesticides are recognized as an important source of potential pollution to soil and water due to their mobility and degradation in soils. Results presented in this paper show impact of the organic complex concentration on the adsorption of herbicides (acetochlor) at the surface of the organic modified montmorillonite. In this work, natural montmorillonite from Bogovina, located near Boljevac municipality, was used for organic modification. Cation-exchange capacity of this montmorillonite was determined by extraction with ammonium acetate (86 mmol/100g of clay). Montmorillonite have been modified first with NaCl and than with two organic complexes, hexadecyltrimethylammonium bromide (HDTMA) and phenyltrimethylammonium chloride (PTMA). For both organic complexes, three saturation concentrations were selected for monitoring of the herbicide adsorption (43 mmol/100g of clay (0.5 CEC), 86 mmol/100g of clay (1 CEC) and 129 mmol/100g of clay (1.5 CEC)). Changes in the properties of the inorganic and organic bentonite have been examined using the X-ray powder diffraction (XRPD) and batch equilibrium method. Increase in basal spacing (d) of montmorillonites saturated with 1.5 CEC of organic cation indicate that sorption of PTMA and HDTMA can exceed the saturation of 1 CEC. Both organic montmorillonites have shown higher uptake of the herbicide, compared to the inorganic montmorillonite. Comparing the values Freundlich coefficients in batch equilibrium method, (presented in the form of log Kf and 1/n), it can be seen that the sorption decreases in the series: 0.5CEC> 1CEC> 1.5CEC> NaM, for both organic montmorillonites.

  9. On the surface topography of ultrashort laser pulse treated steel surfaces

    NASA Astrophysics Data System (ADS)

    Vincenc Obona, J.; Ocelík, V.; Skolski, J. Z. P.; Mitko, V. S.; Römer, G. R. B. E.; Huis in't Veld, A. J.; De Hosson, J. Th. M.

    2011-12-01

    This paper concentrates on observations of the surface topography by scanning electron microscopy (SEM) on alloyed and stainless steels samples treated by ultrashort laser pulses with duration of 210 fs and 6.7 ps. Globular-like and jet-like objects were found depending on the various levels of the fluence applied. It is shown that these features appear due to solid-liquid and liquid-gas transitions within surface layer irradiated by intense laser light. The observations are confronted to the theory of short-pulsed laser light-matter interactions, including interference, excitation of electrons, electron-phonon coupling as well as subsequent ablation. It is shown that the orientation of small ripples does not always depend on the direction of the polarization of laser light.

  10. Spectroscopic ellipsometry studies of HF treated Si (100) surfaces

    NASA Technical Reports Server (NTRS)

    Yao, Huade; Woollam, John A.; Alterovitz, Samuel A.

    1993-01-01

    Both ex situ and in situ spectroscopic ellipsometry (SE) measurements were employed to investigate the effects of HF cleaning on Si surfaces. The hydrogen-terminated (H-terminated) Si surface was modeled as an equivalent dielectric layer, and monitored in real time by SE measurements. The SE analyses indicate that after a 20-s 9:1 HF dip without rinse, the Si(100) surface was passivated by the hydrogen termination and remained chemically stable. Roughness of the HF-etched bare Si(100) surface was observed, in an ultrahigh vacuum (UHV) chamber, and analyzed by the in situ SE. Evidence for desorption of the H-terminated Si surface-layer, after being heated to approximately 550 C in the UHV chamber, is presented and discussed. This is the first use of an ex situ and in situ real-time, nondestructive technique capable of showing state of passivation, the rate of reoxidation, and the surface roughness of the H-terminated Si surfaces.

  11. Spectroscopic ellipsometry studies of HF treated Si (100) surfaces

    NASA Technical Reports Server (NTRS)

    Yao, Huade; Woollam, John A.; Alterovitz, Samuel A.

    1993-01-01

    Both ex situ and in situ spectroscopic ellipsometry (SE) measurements were employed to investigate the effect of HF cleaning on Si surfaces. The hydrogen-terminated (H-terminated) Si surface was modeled as an equivalent dielectric layer, and monitored in real time by SE measurements. The SE analyses indicate that, after a 20-sec 9:1 HF dip without rinse, the Si (100) surface was passivated by the hydrogen termination and remained chemically stable. Roughness of the HF-etched bare Si (100) surface was observed, in an ultrahigh vacuum chamber (UHV), and analyzed by the in situ SE. Evidence for desorption of the H-terminated Si surface layer, after being heated to about 550 C in the UHV chamber, is presented and discussed. This is the first use of an ex situ and in situ real-time, nondestructive technique capable of showing state of passivation, the rate of reoxidation, and the surface roughness of the H-terminated Si surfaces.

  12. Spectroscopic ellipsometry studies of HF treated Si (100) surfaces

    NASA Astrophysics Data System (ADS)

    Yao, Huade; Woollam, John A.; Alterovitz, Samuel A.

    1993-08-01

    Both ex situ and in situ spectroscopic ellipsometry (SE) measurements were employed to investigate the effects of HF cleaning on Si surfaces. The hydrogen-terminated (H-terminated) Si surface was modeled as an equivalent dielectric layer, and monitored in real time by SE measurements. The SE analyses indicate that after a 20-s 9:1 HF dip without rinse, the Si(100) surface was passivated by the hydrogen termination and remained chemically stable. Roughness of the HF-etched bare Si(100) surface was observed, in an ultrahigh vacuum (UHV) chamber, and analyzed by the in situ SE. Evidence for desorption of the H-terminated Si surface-layer, after being heated to approximately 550 C in the UHV chamber, is presented and discussed. This is the first use of an ex situ and in situ real-time, nondestructive technique capable of showing state of passivation, the rate of reoxidation, and the surface roughness of the H-terminated Si surfaces.

  13. Spectroscopic ellipsometry studies of HF treated Si (100) surfaces

    NASA Astrophysics Data System (ADS)

    Yao, Huade; Woollam, John A.; Alterovitz, Samuel A.

    1993-06-01

    Both ex situ and in situ spectroscopic ellipsometry (SE) measurements were employed to investigate the effect of HF cleaning on Si surfaces. The hydrogen-terminated (H-terminated) Si surface was modeled as an equivalent dielectric layer, and monitored in real time by SE measurements. The SE analyses indicate that, after a 20-sec 9:1 HF dip without rinse, the Si (100) surface was passivated by the hydrogen termination and remained chemically stable. Roughness of the HF-etched bare Si (100) surface was observed, in an ultrahigh vacuum chamber (UHV), and analyzed by the in situ SE. Evidence for desorption of the H-terminated Si surface layer, after being heated to about 550 C in the UHV chamber, is presented and discussed. This is the first use of an ex situ and in situ real-time, nondestructive technique capable of showing state of passivation, the rate of reoxidation, and the surface roughness of the H-terminated Si surfaces.

  14. Electrical and optical characteristics of surface treated ZnO nanotubes

    SciTech Connect

    Ranjusha, R.; Sreeja, R.; Mini, P.A.; Subramanian, K.R.V.; Nair, Shantikumar V.; Balakrishnan, Avinash

    2012-08-15

    Highlights: ► ZnO nanotubes were formed onto an ITO glass and were surface treated. ► Photoluminescence and fluorescence imaging for ZnO nanotubes showed blue emission. ► Surface treated samples that showed green emissions. ► Lifetime measurements showed higher excitonic times in surface treated samples. ► Conductance measurements showed significant improvement for the treated samples. -- Abstract: Vertical ZnO nanotubes were electrochemically deposited onto an indium doped tin oxide glass substrate. These nanotubes were surface treated with zinc acetate and annealed at 450 °C, resulting in a nanotubes/nanoparticles composite layer. Scanning electron microscopy of the surface treated samples showed nanoparticles been dispersed uniformly along the ZnO tubular matrix, which was confirmed by X-ray diffractrometry. Photoluminescence and fluorescence microscopy showed untreated ZnO nanotubes exhibiting blue emission, while the treated samples exhibited green emissions. Ultra-violet spectroscopy of treated samples revealed lower band gap values compare to their untreated counterparts. Lifetime measurements showed higher excitonic lifetimes in treated samples. Conductance studies using atomic force microscopy showed significant improvement in the conductance values for the treated samples. A significant increase in photocurrent was observed in treated samples when used as photo-anodes in dye sensitized solar cells.

  15. Magnetic properties of pure and surface-treated vanadium

    SciTech Connect

    DeSchutter, F.; Bruynseraede, Y.; Gilabert, A.

    1983-05-01

    The very high surface pinning present in superconductors strongly hinders the analysis of fission fragment irradiation experiments which produce heavy damage in a surface layer of approximately 10 ..mu..m. In order to decrease this pinning effect, different treatments such as coating with a normal metal or oxygen diffusion can be used. In this paper we show that oxygen doping lowers the critical temperature T /SUB c/ of Vanadium and surface oxidation reduces drastically the irreversibility of magnetization curves. The authors show that the dependence of T /SUB c/ on the oxygen concentration combined with the measurement of the oxygen concentration gradient (obeying Fick's diffusion law) can explain their magnetic permeability data.

  16. Controlled Release of Agrochemicals Intercalated into Montmorillonite Interlayer Space

    PubMed Central

    2014-01-01

    Periodic application of agrochemicals has led to high cost of production and serious environmental pollution. In this study, the ability of montmorillonite (MMT) clay to act as a controlled release carrier for model agrochemical molecules has been investigated. Urea was loaded into MMT by a simple immersion technique while loading of metalaxyl was achieved by a rotary evaporation method. The successful incorporation of the agrochemicals into the interlayer space of MMT was confirmed by several techniques, such as, significant expansion of the interlayer space, reduction of Barrett-Joyner-Halenda (BJH) pore volumes and Brunauer-Emmett-Teller (BET) surface areas, and appearance of urea and metalaxyl characteristic bands on the Fourier-transform infrared spectra of the urea loaded montmorillonite (UMMT) and metalaxyl loaded montmorillonite (RMMT) complexes. Controlled release of the trapped molecules from the matrix was done in water and in the soil. The results reveal slow and sustained release behaviour for UMMT for a period of 10 days in soil. For a period of 30 days, MMT delayed the release of metalaxyl in soil by more than 6 times. It is evident that MMT could be used to improve the efficiency of urea and metalaxyl delivery in the soil. PMID:24696655

  17. FT-IR spectroscopic investigation of adsorption of 3-aminopyridine on sepiolite and montmorillonite from Anatolia

    NASA Astrophysics Data System (ADS)

    Akyüz, S.; Akyüz, T.; Yakar, A. E.

    2001-05-01

    The adsorption of 3-aminopyridine by natural sepiolite and montmorillonite from Eskisehir (Anatolia) was investigated in the temperature range from 20 to 125°C by infrared spectrometry using a variable temperature unit. The spectroscopic results indicate that the 3-aminopyridine molecules adsorbed on sepiolite are coordinated to Lewis acidic sites and/or surface hydroxyls by H-bonding interaction through pyridine ring nitrogen lone pairs. Surface Bronsted acid strength of sepiolite is weak and 3-aminopyridinium is not detected under the conditions applied in this study. It must be noted that the adsorption of aminopyridine affected the hydroxyl group vibrations of sepiolite. The intercalation of 3-aminopyridine within montmorillonite has been shown by X-ray diffraction to increase the interlayer spacing. IR spectroscopy indicates that sorbed 3-aminopyridine molecules by montmorillonite are mostly coordinated to exchangeable cations directly or indirectly through water bridges. The formation of 3-aminopyridinium cation is also detected at elevated temperatures.

  18. Surface chemical composition analysis of heat-treated bamboo

    NASA Astrophysics Data System (ADS)

    Meng, Fan-dan; Yu, Yang-lun; Zhang, Ya-mei; Yu, Wen-ji; Gao, Jian-min

    2016-05-01

    In this study, the effect of heat treatment on the chemical composition of bamboo slivers was studied. The chemical properties of the samples were examined by chemical analysis. Results showed a decrease in the contents of holocellulose and α-cellulose, as well as an increase in the contents of lignin and extractives. Changes in the chemical structure of bamboo components were analyzed by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). FTIR spectroscopy results indicated that hemicellulose contents decrease, whereas lignin contents increase after heat treatment. Ester formation linked to lignin decreased the hygroscopicity of the bamboo samples and consequently improved their dimensional stability and durability. XPS spectroscopy results showed that hemicelluloses and celluloses are relatively more sensitive to the heating process than lignin. As a consequence, hemicellulose and cellulose contents decreased, whereas lignin contents increased during heat treatment. The results obtained in this study provide useful information for the future utilization of heat-treated bamboo.

  19. Bone regeneration performance of surface-treated porous titanium.

    PubMed

    Amin Yavari, Saber; van der Stok, Johan; Chai, Yoke Chin; Wauthle, Ruben; Tahmasebi Birgani, Zeinab; Habibovic, Pamela; Mulier, Michiel; Schrooten, Jan; Weinans, Harrie; Zadpoor, Amir Abbas

    2014-08-01

    The large surface area of highly porous titanium structures produced by additive manufacturing can be modified using biofunctionalizing surface treatments to improve the bone regeneration performance of these otherwise bioinert biomaterials. In this longitudinal study, we applied and compared three types of biofunctionalizing surface treatments, namely acid-alkali (AcAl), alkali-acid-heat treatment (AlAcH), and anodizing-heat treatment (AnH). The effects of treatments on apatite forming ability, cell attachment, cell proliferation, osteogenic gene expression, bone regeneration, biomechanical stability, and bone-biomaterial contact were evaluated using apatite forming ability test, cell culture assays, and animal experiments. It was found that AcAl and AnH work through completely different routes. While AcAl improved the apatite forming ability of as-manufactured (AsM) specimens, it did not have any positive effect on cell attachment, cell proliferation, and osteogenic gene expression. In contrast, AnH did not improve the apatite forming ability of AsM specimens but showed significantly better cell attachment, cell proliferation, and expression of osteogenic markers. The performance of AlAcH in terms of apatite forming ability and cell response was in between both extremes of AnH and AsM. AcAl resulted in significantly larger volumes of newly formed bone within the pores of the scaffold as compared to AnH. Interestingly, larger volumes of regenerated bone did not translate into improved biomechanical stability as AnH exhibited significantly better biomechanical stability as compared to AcAl suggesting that the beneficial effects of cell-nanotopography modulations somehow surpassed the benefits of improved apatite forming ability. In conclusion, the applied surface treatments have considerable effects on apatite forming ability, cell attachment, cell proliferation, and bone ingrowth of the studied biomaterials. The relationship between these properties and the bone

  20. Surface Treated Natural Fibres as Filler in Biocomposites

    NASA Astrophysics Data System (ADS)

    Schwarzova, I.; Stevulova, N.; Singovszka, E.; Terpakova, E.

    2015-11-01

    Biocomposites based on natural fibres as organic filler have been studied for several years because traditional building materials such as concrete are increasingly being replaced by advanced composite materials. Natural fibres are a potential replacement of glass fibres in composite materials. Inherent advantages such as low density, biodegradability and comparable specific mechanical properties make natural fibres an attractive option. However, limitations such as poor thermal stability, moisture absorption and poor compatibility with matrix are challenges that need to be resolved. The primary objective of this research was to study the effect of surface treatment on properties of hemp hurds like a natural lignocellulosic material and composites made thereof. Industrial hemp fibre is the one of the most suitable fibres for use in composite materials because of its good specific properties, as well as it being biologically degradable and CO2 neutral. Improving interfacial bonding between fibres and matrix is an important factor in using hemp fibres as reinforcement in composites. In order to improve interfacial bonding, modifications can be made to the hemp fibres to remove non- cellulosic compounds, separate hemp fibres from their bundles, and modify the fibre surface. This paper contains the comparison of FTIR spectra caused by combination of physical and chemical treatment of hemp material with unmodified sample. Modification of hemp hurds was carried out by NaOH solution and by ultrasonic treatment (deionized water and NaOH solution were used as the cleaning mediums).

  1. Exfoliation of montmorillonite in protein solutions.

    PubMed

    Kolman, Krzysztof; Steffen, Werner; Bugla-Płoskońska, Gabriela; Skwara, Aleksandra; Pigłowski, Jacek; Butt, Hans-Jürgen; Kiersnowski, Adam

    2012-05-15

    In the study we demonstrate a method to obtain stable, exfoliated montmorillonite-protein complexes by adsorption of the proteins extracted from hen-egg albumen. Analysis of the process by means of sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) revealed that the complexes are formed by sequential adsorption of ovotransferrin, ovalbumins, ovomucoid and lysozyme on the surface of the silicate. Structural studies performed by X-ray diffraction (XRD) and transmission electron microscopy (TEM) indicated that the adsorption of ovotransferrin and albumins is accompanied by disintegration of clay stacks into discrete platelets. Further analysis by dynamic light scattering (DLS) revealed that at protein to silicate weight ratios exceeding 20, the synergistic adsorption of albumen components leads to reaggregation of silicate platelets into disordered, microgel-like particles. By means of DLS it was found that exfoliation predominantly leads to formation of particles with average hydrodynamic radii (R(h)) of 0.19 μm while their aggregation causes formation of particles having R(h) in of approx. 0.5 μm and larger. PMID:22405581

  2. Montmorillonite nanodevices for the colon metronidazole delivery.

    PubMed

    Calabrese, Ilaria; Cavallaro, Gennara; Scialabba, Cinzia; Licciardi, Mariano; Merli, Marcello; Sciascia, Luciana; Turco Liveri, Maria Liria

    2013-11-30

    The adsorption profiles of the antibiotic metronidazole (MNE) into the K10-montmorillonite (MMT-K10) clay and the subsequent release have been investigated as a function of pH and MNE/MMT-K10 ratio, in order to evaluate the potential of the MNE/MMT-K10 hybrids as controlled drug delivery system. The adsorption mechanism has been first elucidated by performing complementary equilibrium and kinetic studies and through the X-ray diffractometry (XRD) characterization of the obtained composite materials. The gathered results allowed us to propose a mechanism consisting of a multi-step pathway involving the neutral and the cationic form of the drug, which interact with different sites of the clay surfaces, i.e. the interlayer region and the faces of the lamella. In a second step the drug release kinetics has been studied under physiological pH mimicking conditions simulating the oral drug administration and delivery. For the sake of comparison the commercial formulation has also been employed for the release studies. The investigation of the release profiles and the comparison with the commercial formulation of the drug reveal that the new-tailor made formulation could be fruitful exploited for successfully prolonged the action of drug in the desired site. PMID:24076230

  3. A study of purified montmorillonite intercalated with 5-fluorouracil as drug carrier.

    PubMed

    Lin, F H; Lee, Y H; Jian, C H; Wong, Jau-Min; Shieh, Ming-Jium; Wang, Cheng-Yi

    2002-05-01

    Since its introduction over 40 years ago, 5-fluorouracil (5-FU) has remained the only effective chemotherapy option available for the treatment of colorectal cancer (CRC). However, this cytotoxic anticancer drug often causes severe side effects because it does not act selectively on the tumor. It has been reported that the 5-FU showed considerable toxicity when administered by intravenous injections or via alimentary tract. Although, many materials have been developed for carrying 5-FU, there has been no clinically acceptable carrier for 5-FU till now. Montmorillonite, one of the clay minerals, consists of hydrated aluminum silicates with fine grains and large spaces between the layers. Isomorphous substitution of cations is common. In the study, we attempt to intercalate 5-FU into interlayers of montmorillonite through ion exchange. Montmorillonite was purified from crude clays of bentonite in Tai-dong, Taiwan by filtration and sedimentation. Solutions of 5-FU with different concentrations were prepared by dissolving various amounts of 5-FU into 10 ml NaOH solution. Purified montmorillonite powder was soaked in 5-FU solution for a period of time with different pH values and temperatures. In this study, we try to intercalate 5-FU into interlayers of montmorillonite to find out optimum conditions, such as soaking time, temperature, pH value, initial 5-FU concentration, etc., to prepare composites of 5-FU and montmorillonite (5-FU/mont). UV, SDT, FTIR, XRD are used to characterize the 5-FU/mont composite. From the results. 5-FU was successfully intercalated into the interlayer of montmorillonite both by free surface absorption and OH replacement. The optimum condition for 5-FU/mont preparations is 1.185 wt% of 5-FU as initial concentration under a pH value of 11.6 at a temperature of 80 degrees C and a soaking time of 2 h. The total amount of 5-FU in montmorillonite is about 87.5 mg for each gram of montmorillonite, which can be proved by thermal gravimetric analysis

  4. Fractionation of humic acids upon adsorption on montmorillonite and palygorskite

    NASA Astrophysics Data System (ADS)

    Alekseeva, T. V.; Zolotareva, B. N.

    2013-06-01

    The adsorption of three humic acid (HA) preparations by clays—montmorillonite (Wyoming, USA) and palygorskite (Kolomenskoe district, Moscow oblast)—has been studied. The HA preparations were isolated from samples of the humus-accumulative horizons of a leached chernozem (Voronezh) and a chestnut soil (Volgograd), and a commercial preparation of sodium humate (Aldrich) was also used. The solid-state 13C NMR spectroscopy and IR spectroscopy revealed the selective adsorption of structural HA fragments (alkyls, O-alkyls (carbohydrates), and acetal groups) on these minerals. As a result, the aromaticity of the organic matter (OM) in the organic-mineral complexes (OMCs) and the degree of its humification have been found to be lower compared to the original HA preparations. The fractionation of HAs is controlled by the properties of the mineral surfaces. The predominant enrichment of OMCs with alkyls has been observed for montmorillonite, as well as an enrichment with O-alkyls (carbohydrates) for palygorskite. A decrease in the C : N ratio has been noted in the elemental composition of the OM in complexes, which reflected its more aromatic nature and (or) predominant sorption of N-containing structural components of HA molecules. The adsorption of HA preparations by montmorillonite predominantly occurs on the external surface of mineral particles, and the interaction of nonpolar alkyl groups of HAs with this mineral belongs to weak (van der Waals, hydrophobic) interactions. The adsorption of HA preparations by palygorskite is at least partly of chemical nature: Si-OH groups of minerals are involved in the adsorption process. The formation of strong bonds between the OM and palygorskite explains the long-term (over 300 million years) retention of fossil fulvate-type OM in its complex with palygorskite, which we revealed previously.

  5. Investigation on surface structure of potassium permanganate/nitric acid treated poly(tetrafluoroethylene)

    NASA Astrophysics Data System (ADS)

    Fu, Congli; Liu, Shuling; Gong, Tianlong; Gu, Aiqun; Yu, Zili

    2014-10-01

    In the previous articles concerning the treatment of poly(tetrafluoroethylene) (PTFE) with potassium permanganate/nitric acid mixture, the conversion of a hydrophobic to a hydrophilic surface was partially assigned to the defluorination of PTFE and then the introduction of carbonyl and hydroxyl groups into the defluorinated sites. In the present work, PTFE sheets were treated with potassium permanganate/nitric acid, and the surfaces before and after treatment were comparatively characterized by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The surface sediments of the treated PTFE were also determined by atomic absorption spectroscopy (AAS). The results indicate that the conversion of the hydrophobicity to the hydrophilicity on the modified PTFE surface is mainly due to the deposition of hydrophilic manganese oxides which covered the fluorocarbon surface, and no detectable chemical reactions of PTFE occur in the treating process.

  6. MALDI analysis of oligonucleotides directly from montmorillonite.

    PubMed

    Zagorevskii, Dmitri V; Aldersley, Michael F; Ferris, James P

    2006-09-01

    Oligonucleotides synthesized on a montmorillonite catalyst were analyzed directly. By mixing the catalyst with a matrix (2,4,6-trihydroxyacetophenone or 6-aza-2-thiothymine) and dibasic ammonium citrate, higher molecular weight products were detected compared with "classical" methods such as gel electrophoresis and HPLC with UV as a detector. The oligomers (30-mers and higher) were detected by mass spectrometry even though their concentration was less than 10(-4)% of the total content of the RNA. This method is different from the (MALDI) analysis of the eluates from montmorillonite, which otherwise requires desalting. Placing reaction mixtures with a high concentration of buffers on homoionic, preferably Li-containing, montmorillonite does not require desalting. PMID:16809045

  7. Amino acid conjugated self assembling molecules for enhancing surface wettability of fiber laser treated titanium surfaces

    NASA Astrophysics Data System (ADS)

    Akkan, Cagri K.; Hür, Deniz; Uzun, Lokman; Garipcan, Bora

    2016-03-01

    Surface wetting properties of implants are one of the most critical parameter, which determine the interaction of proteins and cells with the implant surface. In this regards, acid etching and sand blasting are the mostly used methods at surface modification of Titanium (Ti) for enhanced surface wettability. Besides, these kinds of modifications may cause a conflict whether the surface wettability is influenced by the process related surface contaminations or by the surface roughness. In contrast, lasers might be an option for the alteration of surface wetting properties via supporting micro and/or nano surface topographies while preventing surface chemical contaminations. In this work, we focused on two steps of surface processing approaches of Ti surface: physical and chemical modifications. Herein, we hierarchically structured Ti surfaces by using microsecond modulated pulsed fiber laser. Subsequently, laser structured and non-structured Ti surfaces were further modified with novel histidine and leucine Amino Acid conjugated Self-Assembled Molecules (His1-SAMs2 and Leu3-SAMs) to alter the surface wettability by introducing biologically hydrophilic and hydrophobic groups. Modification of Ti surfaces with His-SAMs and Leu-SAMs ended up with stable wetting properties when compared to non-modified surfaces after 7 days which may enhances the cell-surface interaction.

  8. Self-Cleaning Features of Plasma-Treated Surfaces with Self-Assembled Monolayer Coating

    NASA Astrophysics Data System (ADS)

    Lee, Sang‑Joon; Paik, Bu‑Geun; Kim, Guk‑Bae; Jang, Young‑Gil

    2006-02-01

    A biomimic surface was coated onto a poly(tetrafluoroethylene) (PTFE) substrate. The coated PTFE surface was found to have nanoscale roughness and high hydrophobicity. In the first preparation step, the PTFE surface was modified by plasma etching. A self-assembled monolayer (SAM) of octadecyltrichlorosilane (ODTS) was then deposited onto the modified surface with a thickness of a 2-3 nm. This surface was found to have self-cleaning features similar to those of a lotus leaf. The self-cleaning features were confirmed by comparing the contact and sliding angles of the original PTFE surface, a PTFE surface plasma treated, and a PTFE surface plasma treated and SAM coated. The PTFE surface treated with plasma and SAM coated had an increased contact angle and a decreased sliding angle compared with the other surfaces. It also exhibited increased stability and slow aging. The quantity of oxygen-containing groups that can be greatly influenced by plasma treatment, SAM coating, and aging, seems to play an important role in surface modification.

  9. 40 CFR 721.10573 - Magnesium hydroxide surface treated with substituted alkoxysilanes (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Magnesium hydroxide surface treated... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10573 Magnesium hydroxide surface... to reporting. (1) The chemical substance identified generically as magnesium hydroxide...

  10. 40 CFR 721.10573 - Magnesium hydroxide surface treated with substituted alkoxysilanes (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Magnesium hydroxide surface treated... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10573 Magnesium hydroxide surface... to reporting. (1) The chemical substance identified generically as magnesium hydroxide...

  11. Extending a transonic small disturbance code to treat swept vertical surfaces

    NASA Technical Reports Server (NTRS)

    Gibbons, Michael D.

    1992-01-01

    A flexible-swept vertical surface capability has been developed and implemented within the CAP-TSD transonic small disturbance (TSD) code. The new capability required a modification to the TSD equation and a grid transformation for swept vertical surfaces. Modifications to the vertical surface boundary conditions allow it to be treated as a flexible surface. The new capability extends the range of problems which the code can treat. In order to assess the accuracy of the modifications, calculations were performed for a rectangular T-tail configuration and an AGARD T-tail configuration. Unsteady forces and moments are presented for the rectangular T-tail oscillating in yaw for a range of reduced frequencies. Comparisons are presented with linear theory and experiment. Steady and unsteady surface pressures are presented for the AGARD T-tail along with generalized aerodynamic forces. Comparisons are made with linear theory. The comparisons demonstrate the accuracy of the vertical surface modifications.

  12. Synthesis and Characterization of the Hybrid Clay- Based Material Montmorillonite-Melanoidin: A Potential Soil Model

    SciTech Connect

    V Vilas; B Matthiasch; J Huth; J Kratz; S Rubert de la Rosa; P Michel; T Schäfer

    2011-12-31

    The study of the interactions among metals, minerals, and humic substances is essential in understanding the migration of inorganic pollutants in the geosphere. A considerable amount of organic matter in the environment is associated with clay minerals. To understand the role of organic matter in the environment and its association with clay minerals, a hybrid clay-based material (HCM), montmorillonite (STx-1)-melanoidin, was prepared from L-tyrosine and L-glutamic acid by the Maillard reaction. The HCM was characterized by elemental analysis, nuclear magnetic resonance, x-ray photoelectron spectroscopy (XPS), scanning transmission x-ray microscopy (STXM), and thermal analysis. The presence of organic materials on the surface was confirmed by XPS and STXM. The STXM results showed the presence of organic spots on the surface of the STx-1 and the characterization of the functional groups present in those spots. Thermal analysis confirmed the existence of organic materials in the montmorillonite interlayer, indicating the formation of a composite of melanoidin and montmorillonite. The melanoidin appeared to be located partially between the layers of montmorillonite and partially at the surface, forming a structure that resembles the way a cork sits on the top of a champagne bottle.

  13. Pu(V) and Pu(IV) sorption to montmorillonite.

    PubMed

    Begg, James D; Zavarin, Mavrik; Zhao, Pihong; Tumey, Scott J; Powell, Brian; Kersting, Annie B

    2013-05-21

    Plutonium (Pu) adsorption to and desorption from mineral phases plays a key role in controlling the environmental mobility of Pu. Here we assess whether the adsorption behavior of Pu at concentrations used in typical laboratory studies (≥10(-10) [Pu] ≤ 10(-6) M) are representative of adsorption behavior at concentrations measured in natural subsurface waters (generally <10(-12) M). Pu(V) sorption to Na-montmorillonite was examined over a wide range of initial Pu concentrations (10(-6)-10(-16) M). Pu(V) adsorption after 30 days was linear over the wide range of concentrations studied, indicating that Pu sorption behavior from laboratory studies at higher concentrations can be extrapolated to sorption behavior at low, environmentally relevant concentrations. Pu(IV) sorption to montmorillonite was studied at initial concentrations of 10(-6)-10(-11) M and was much faster than Pu(V) sorption over the 30 day equilibration period. However, after one year of equilibration, the extent of Pu(V) adsorption was similar to that observed for Pu(IV) after 30 days. The continued uptake of Pu(V) is attributed to a slow, surface-mediated reduction of Pu(V) to Pu(IV). Comparison between rates of adsorption of Pu(V) to montmorillonite and a range of other minerals (hematite, goethite, magnetite, groutite, corundum, diaspore, and quartz) found that minerals containing significant Fe and Mn (hematite, goethite, magnetite, and groutite) adsorbed Pu(V) faster than those which did not, highlighting the potential importance of minerals with redox couples in increasing the rate of Pu(V) removal from solution. PMID:23614502

  14. Mouse embryonic fibroblasts accumulate differentially on titanium surfaces treated with nanosecond laser pulses.

    PubMed

    Radmanesh, Mitra; Ektesabi, Amin M; Wyatt, Rachael A; Crawford, Bryan D; Kiani, Amirkianoosh

    2016-01-01

    Biomaterial engineering, specifically in bone implant and osseointegration, is currently facing a critical challenge regarding the response of cells to foreign objects and general biocompatibility of the materials used in the production of these implants. Using the developing technology of the laser surface treatment, this study investigates the effects of the laser repetition rate (frequency) on cell distribution across the surface of the titanium substrates. The main objective of this research is building a fundamental understanding of how cells interact with treated titanium and how different treatments affect cell accumulation. Cells respond differently to surfaces treated with different frequency lasers. The results of this research identify the influence of frequency on surface topography properties and oxidation of titanium, and their subsequent effects on the pattern of cell accumulation on its surface. Despite increased oxidation in laser-treated regions, the authors observe that fibroblast cells prefer untreated titanium to laser-treated regions, except the regions treated with 25 kHz pulses, which become preferentially colonized after 72 h. PMID:27581527

  15. Staphylococcus epidermidis adhesion on surface-treated open-cell Ti6Al4V foams.

    PubMed

    Türkan, Uğur; Güden, Mustafa; Sudağıdan, Mert

    2016-06-01

    The effect of alkali and nitric acid surface treatments on the adhesion of Staphylococcus epidermidis to the surface of 60% porous open-cell Ti6Al4V foam was investigated. The resultant surface roughness of foam particles was determined from the ground flat surfaces of thin foam specimens. Alkali treatment formed a porous, rough Na2Ti5O11 surface layer on Ti6Al4V particles, while nitric acid treatment increased the number of undulations on foam flat and particle surfaces, leading to the development of finer surface topographical features. Both surface treatments increased the nanometric-scale surface roughness of particles and the number of bacteria adhering to the surface, while the adhesion was found to be significantly higher in alkali-treated foam sample. The significant increase in the number of bacterial attachment on the alkali-treated sample was attributed to the formation of a highly porous and nanorough Na2Ti5O11 surface layer. PMID:26057214

  16. Characterization of the surface and the interphase of PVC-copper amine-treated wood composites

    NASA Astrophysics Data System (ADS)

    Jiang, Haihong; Kamdem, D. Pascal

    2010-05-01

    Contact angles and surface energy of wood, as well as interfacial shear strength between wood and polyvinyl chloride (PVC) were investigated and used to monitor the modifications generated on the surfaces of wood treated with a copper ethanolamine solution. An increase in surface energy of wood after treatments promotes wetting of PVC on wood surfaces. Improved interfacial shear strength between treated wood and PVC matrix can be attributed to the formation of a stronger wood-PVC interphase. This suggests that treatment may be used to improve the adhesion between wood surface and PVC in the formulation of wood fiber composites to yield products with enhanced mechanical properties and better biological and physical performance against decay and insect destroying wood.

  17. Surface characteristics analysis of polypropylene treated by dielectric barrier discharge at atmospheric pressure

    NASA Astrophysics Data System (ADS)

    Nishime, T. M. C.; Toth, A.; Hein, L. R. O.; Kostov, K. G.

    2012-06-01

    Polypropylene (PP) samples were treated by Dielectric Barrier Discharge (DBD) in order to modify their surface characteristics. The XPS analysis reveals that the DBD treatment added oxygen atoms to the PP surface. These polar groups cause increase in the wettability as shown by water contact angle measurements. The formation of low-molecular-weight oxidized materials (LMWOMs) in the form of small nodules on the PP surface was observed by atomic force microscopy (AFM). The presence of oxygen polar groups on the PP surface was also confirmed by infrared spectroscopy (FTIR). All analysis were performed before and after rinsing the treated samples in water and showed that the LMWOM can be removed from the surface by polar solvents.

  18. Surface characterization of alkali- and heat-treated Ti with or without prior acid etching

    NASA Astrophysics Data System (ADS)

    An, Sang-Hyun; Matsumoto, Takuya; Miyajima, Hiroyuki; Sasaki, Jun-Ichi; Narayanan, Ramaswamy; Kim, Kyo-Han

    2012-03-01

    Titanium and its alloys are used as implant materials in dental and orthopaedic applications. The material affinities to host bone tissue greatly concern with the recovery period and good prognosis. To obtain a material surface having excellent affinity to bone, acid etching prior to alkali- and heat-treatment of Ti was conducted. The surface characteristics of the prepared sample indicated that the roughness as well as the wettability increased by pre-etching. Bone-like apatite was formed on pre-etched, alkali- and heat-treated Ti surface in simulated body fluid (SBF) within 3 days, while it takes 5 days on the solely alkali- and heat-treated surface. Osteoblastic cells showed better compatibility on the per-etched surface compared to the pure Ti surface or alkali- and heat-treated surface. Moreover, the pre-etched surface showed better pull-off tensile adhesion strength against the deposited apatite. Thus, acid etching prior to alkali- and heat-treatment would be a promising method for enhancing the affinity of Ti to host bone tissue.

  19. Surface modification of argon/oxygen plasma treated vulcanized ethylene propylene diene polymethylene surfaces for improved adhesion with natural rubber

    NASA Astrophysics Data System (ADS)

    Basak, Ganesh C.; Bandyopadhyay, Abhijit; Neogi, Sudarsan; Bhowmick, Anil K.

    2011-01-01

    Vulcanized ethylene propylene diene polymethylene (EPDM) rubber surface was treated in a radio frequency capacitatively coupled low pressure argon/oxygen plasma to improve adhesion with compounded natural rubber (NR) during co-vulcanization. The plasma modified surfaces were analyzed by means of contact angle measurement, surface energy, attenuated total reflection-infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, energy dispersive X-ray sulfur mapping and atomic force microscopy. Several experimental variables such as plasma power, length of exposure time and composition of the argon-oxygen gas mixture were considered. It was delineated that plasma treatment changed both surface composition and roughness, and consequently increased peel strength. The change in surface composition was mainly ascribed to the formation of C-O and -Cdbnd O functional groups on the vulcanized surfaces. A maximum of 98% improvement in peel strength was observed after plasma treatment.

  20. Immobilization of Bone Morphogenetic Protein on DOPA- or Dopamine-Treated Titanium Surfaces to Enhance Osseointegration

    PubMed Central

    Kang, Jeonghwa; Tada, Seiichi; Kitajima, Takashi; Son, Tae Il; Aigaki, Toshiro; Ito, Yoshihiro

    2013-01-01

    Titanium was treated with 3,4-dihydroxy-L-phenylalanine (DOPA) or dopamine to immobilize bone morphogenetic protein-2 (BMP2), a biomolecule. DOPA and dopamine solutions turned into suspensions, and precipitates were produced at high pH. Both treatments produced a brown surface on titanium that was thicker at high pH than low pH. Dopamine produced a thicker layer than DOPA. The hydrophobicity of the surfaces increased after treatment with dopamine independent of pH. Furthermore, there were more amino groups in the layers formed at pH 8.5 than pH 4.5 in both treatments. Dopamine treatment produced more amino groups in the layer than DOPA. BMP2 was immobilized on the treated surfaces via a coupling reaction using carbodiimide. More BMP2 was immobilized on surfaces treated at pH 8.5 than pH 4.5 in both treatments. The immobilized BMP induced specific signal transduction and alkali phosphatase, a differentiation marker. Thus, the present study demonstrates that titanium treated with DOPA or dopamine can become bioactive via the surface immobilization of BMP2, which induces specific signal transduction. PMID:24459666

  1. Cellular Performance Comparison of Biomimetic Calcium Phosphate Coating and Alkaline-Treated Titanium Surface

    PubMed Central

    Wei, Mei

    2013-01-01

    The influence of biomimetic calcium phosphate coating on osteoblasts behavior in vitro is not well established yet. In this study, we investigated the behavior of osteoblastic rat osteosarcoma 17/2.8 cells (ROS17/2.8) on two groups of biomaterial surfaces: alkaline-treated titanium surface (ATT) and biomimetic calcium phosphate coated ATT (CaP). The cell attachment, proliferation, differentiation, and morphology on these surfaces were extensively evaluated to reveal the impact of substrate surface on osteoblastic cell responses. It was found that the ROS17/2.8 cells cultured on the ATT surface had higher attachment and proliferation rates compared to those on the CaP surface. Our results also showed that the calcium phosphate coatings generated in this work have an inhibiting effect on osteoblast adhesion and further influenced the proliferation and differentiation of osteoblast compared to the ATT surface in vitro. Cells on the ATT surface also exhibited a higher alkaline phosphatase activity than on the CaP surface after two weeks of culture. Immunofluorescence staining and scanning electron microscopy results showed that the cells adhered and spread faster on the ATT surface than on the CaP surface. These results collectively suggested that substrate surface properties directly influence cell adhesion on different biomaterials, which would result in further influence on the cell proliferation and differentiation. PMID:24455730

  2. Montmorillonite, Oligonucleotides, RNA and Origin of Life

    NASA Astrophysics Data System (ADS)

    Ertem, Gözen

    2004-12-01

    Na-montmorillonite prepared from Volclay by the titration method facilitates the self-condensation of ImpA, the 5'-phosphorimidazolide derivative of adenosine. As was shown by AE-HPLC analysis and selective enzymatic hydrolysis of products, oligo(A)s formed in this reaction are 10 monomer units long and contain 67% 3',5'-phosphodiester bonds (Ferris and Ertem, 1992a). Under the same reaction conditions, 5'-phosphorimidazolide derivatives of cytidine, uridine and guanosine also undergo self-condensation producing oligomers containing up to 12-14 monomer units for oligo(C)s to 6 monomer units for oligo(G)s. In oligo(C)s and oligo(U)s, 75-80% of the monomers are linked by 2',5'-phosphodiester bonds. Hexamer and higher oligomers isolated from synthetic oligo(C)s formed by montmorillonite catalysis, which contain both 3',5'- and 2',5'-linkages, serve as catalysts for the non-enzymatic template directed synthesis of oligo(G)s from activated monomer 2-MeImpG, guanosine 5'-phospho-2-methylimidazolide (Ertem and Ferris, 1996). Pentamer and higher oligomers containing exclusively 2',5'-linkages, which were isolated from the synthetic oligo(C)s, also serve as templates and produce oligo(G)s with both 2',5'- and 3',5'-phosphodiester bonds. Kinetic studies on montmorillonite catalyzed elongation rates of oligomers using the computer program SIMFIT demonstrated that the rate constants for the formation of oligo(A)s increased in the order of 2-mer <3-mer <4-mer ... <7-mer (Kawamura and Ferris, 1994). A decameric primer, dA(pdA)8pA bound to montmorillonite was elongated to contain up to 50 monomer units by daily addition of activated monomer ImpA to the reaction mixture (Ferris, Hill and Orgel, 1996). Analysis of dimer fractions formed in the montmorillonite catalyzed reaction of binary and quaternary mixtures of ImpA, ImpC, 2-MeImpG and ImpU suggested that only a limited number of oligomers could have formed on the primitive Earth rather than equal amounts of all possible isomers

  3. Montmorillonite, oligonucleotides, RNA and origin of life

    NASA Technical Reports Server (NTRS)

    Ertem, Gozen

    2004-01-01

    Na-montmorillonite prepared from Volclay by the titration method facilitates the self-condensation of ImpA, the 5'-phosphorimidazolide derivative of adenosine. As was shown by AE-HPLC analysis and selective enzymatic hydrolysis of products, oligo(A)s formed in this reaction are 10 monomer units long and contain 67% 3',5'-phosphodiester bonds (Ferris and Ertem, 1992a). Under the same reaction conditions, 5'-phosphorimidazolide derivatives of cytidine, uridine and guanosine also undergo self-condensation producing oligomers containing up to 12-14 monomer units for oligo(C)s to 6 monomer units for oligo(G)s. In oligo(C)s and oligo(U)s, 75-80% of the monomers are linked by 2',5'-phosphodiester bonds. Hexamer and higher oligomers isolated from synthetic oligo(C)s formed by montmorillonite catalysis, which contain both 3',5'- and 2',5'-linkages, serve as catalysts for the non-enzymatic template directed synthesis of oligo(G)s from activated monomer 2-MeImpG, guanosine 5'-phospho-2-methylimidazolide (Ertem and Ferris, 1996). Pentamer and higher oligomers containing exclusively 2',5'-linkages, which were isolated from the synthetic oligo(C)s, also serve as templates and produce oligo(G)s with both 2',5'- and 3',5'-phosphodiester bonds. Kinetic studies on montmorillonite catalyzed elongation rates of oligomers using the computer program SIMFIT demonstrated that the rate constants for the formation of oligo(A)s increased in the order of 2-mer < 3-mer < 4-mer ... < 7-mer (Kawamura and Ferris, 1994). A decameric primer, dA(pdA)8pA bound to montmorillonite was elongated to contain up to 50 monomer units by daily addition of activated monomer ImpA to the reaction mixture (Ferris, Hill and Orgel, 1996). Analysis of dimer fractions formed in the montmorillonite catalyzed reaction of binary and quaternary mixtures of ImpA, ImpC, 2-MeImpG and ImpU suggested that only a limited number of oligomers could have formed on the primitive Earth rather than equal amounts of all possible

  4. 40 CFR 721.10223 - Styrenyl surface treated manganese ferrite with acrylic ester polymer (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC SUBSTANCES CONTROL ACT SIGNIFICANT NEW USES OF CHEMICAL SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10223 Styrenyl surface treated manganese ferrite with acrylic ester polymer (generic). (a) Chemical substance and significant new...

  5. Study on the surface properties of wood/polyethylene composites treated under plasma

    NASA Astrophysics Data System (ADS)

    Liu, Yang; Tao, Yan; Lv, Xinying; Zhang, Yanhua; Di, Mingwei

    2010-11-01

    Wood/polyethylene (PE) composites are widely used in many fields for its excellent properties, but they are hard to adhere for the surface lacking of polarity. So low-pressure glow discharge of air plasma was used to improve the adhesion properties of wood/PE composites. The composites were treated by plasma under different discharge power. And the changes on the surface properties of the treated and untreated composites were studied by contact angle, Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), atomic force microscope (AFM) and X-ray photoelectron spectroscopy (XPS) analysis. The measurement showed that the contact angle decreased after plasma treatment, and the contact angle decreased gradually with the increasing of discharge power. The FTIR analysis results showed that the polar groups such as hydroxyl, carbonyl and carboxyl were formed on the surface of the composites treated under plasma. SEM and AFM results showed that the roughness of plasma treated samples increased. XPS analysis results indicated that the content of carbon element decreased while the content of oxygen element in the composition of wood/PE composites surface element increased and it reached a balance in a higher power, meanwhile a lot of carboxyl groups were formed. The newly formed polar groups are benefit for the adhesion of composites. The shear bonding strength test showed that the adhesion properties of wood/PE composites improved effectively after plasma treatment.

  6. Preparation and characterization of antibacterial silver/vermiculites and silver/montmorillonites

    NASA Astrophysics Data System (ADS)

    Valášková, Marta; Hundáková, Marianna; Kutláková, Kateřina Mamulová; Seidlerová, Jana; Čapková, Pavla; Pazdziora, Erich; Matějová, Kateřina; Heřmánek, Martin; Klemm, Volker; Rafaja, David

    2010-11-01

    The reason for the preparation and characterization of the novel antibacterial silver/vermiculites (Ag/V) together with the silver/montmorillonites (Ag/M) was that the information on the vermiculite structure change and stability of Ag/V in water as well as its effect on bacteria are sporadic. The vermiculite (V), (Si 3.02Al 0.98) IV (Mg 2.27Al 0.12Fe0.283+Fe0.052+Ti 0.07) VI O 10(OH) 2 Ca 0.09Na 0.21K 0.50 from West China and montmorillonite (M), (Si 3.96Al 0.04) IV (Al 1.20Fe0.343+Mg 0.42Ti 0.02) VI O 10 (OH) 2Ca 0.15Na 0.14K 0.08 from Ivančice (Czech Republic), fraction <0.4 μm were the starting clay materials for sample preparation. The samples V1 and M1 were prepared via reaction of the V and M with the 0.01 mol L -1 AgNO 3 aqueous solution. The samples V2 and M2 were treated with the aqueous solution of AgNO 3 for two times. The cation exchange and reduced metallic silver on M1 and V1 evoked the specific surface area (SSA) diminution, the mean particle-size diameter extension and appearance of micropores with radius (<0.4 nm). Repeated silver cation exchange in M2 and V2 reduced particle size, increased slightly SSA and micropores with radius of 0.4-0.5 nm. Samples Ag/V and Ag/M showed higher content of pores with radius 0.5-1.0 nm than original V and M. The Ag concentration was found higher in Ag/V than in Ag/M and higher in repeatedly treated samples: 0.9 wt.% Ag in V1, 1.4 wt.% Ag in V2, 0.6 wt.% Ag in M1 and 1.0 wt.% Ag in M2. Vermiculite structure consisting of the hydrated interstratified phases and the mica-like phase changed to the cation-one-zero layer hydrate interstratification structure in V1 and to the random of two-one layer hydrate interstratifications in V2. Infrared and Mössbauer spectroscopy revealed no changes in the structure of the clay minerals that could be related directly to the sorption and crystallization of silver. Transmission electron microscopy showed that the silver nanoparticles size distribution was much narrower for the

  7. Further work on sodium montmorillonite as catalyst for the polymerization of activated amino acids

    NASA Technical Reports Server (NTRS)

    Eirich, F. R.; Paecht-Horowitz, M.

    1986-01-01

    When the polycondensation of amino acid acylates was catalyzed with Na-montmorillonite, the polypeptides were consistently found to exhibit a distribution of discrete molecular weights, for as yet undiscovered reasons. One possible explanation was connected to the stepwise mode of monomer addition. New experiments have eliminated this possibility, so that there is the general assumption that this discreteness is the result of a preference of shorter oligomers to add to others of the same length, a feature that could be attributed to some structure of the platelet aggregates of the montmorillonite. The production of optical stereoisomers is anticipated when D,L-amino acids are polymerized on montmorillonite. Having used an optically active surface, the essence of the results lies not only in the occurrence of optically active oligomers and polymers, but also in the fact that the latter exhibit the same molecular weight characteristics as the D,L-polymers. Preparatory to work contemplated on a parallel synthesis of amino acid and nucleotide oligomers, studies were continued on the co-adsorption of amino acids, nucleotides, and amino acid-nucleotides on montmorillonite.

  8. XPS investigation on vacuum thermal desorption of UV/ozone treated GaAs(100) surfaces

    NASA Astrophysics Data System (ADS)

    Cossu, G.; Ingo, G. M.; Mattogno, G.; Padeletti, G.; Proietti, G. M.

    In order to prepare suitable surfaces for molecular beam epitaxy (MBE), sacrificial thin oxide layers on HCl etched GaAs(100) surfaces were grown by both air and UV/ozone exposure. Passive films were subsequently removed by vacuum thermal desorption to achieve surfaces that were smooth and clean on an atomic scale. The evolution of the surface chemical composition, as a function of vacuum desorption temperature, has been studied by means of X-ray photoelectron spectroscopy (XPS). XPS results have evidenced for air and UV/ozone exposed GaAs(100) surfaces a relationship between desorption temperature and surface chemical composition; indeed, the oxide removal is temperature dependent and sequentially selective as follows: As 2O 3. AsO and Ga 2O 3. Furthermore, XPS results have shown that air-grown films have a chemical composition and thermal desorption behaviour different from UV/ozone treated materials. Indeed, these latter have an As 2O 3/Ga 2O 3 and an unoxidized As/Ga ratio close to unity for as grown and thermal treated at 580°C surfaces, respectively. By contrast, air-exposed GaAs(100) materials are Ga 2O 3-enriched and after vacuum thermal desorption treatments have never a stoichiometric composition(As (GaAs)/Ga (GaAs)= 1). Furthermore UV/ozone treated GaAs(100) surfaces subjected to a vacuum thermal treatment at 580°C, have a troublesome organic contamination level below XPS detectability, whereas from air-exposed surfaces, carbon is not completely thermally removable

  9. Preparation and Characterization of Novel Montmorillonite Nanocomposites

    NASA Astrophysics Data System (ADS)

    Mansa, Rola

    Clay minerals have historically played a consequential role in human health. While the beginnings were rooted in geophagy, a primitive act of consuming earth, the health-related uses of clay minerals have evolved and diversified over time.. As excipients in pharmaceutical formulations, clay minerals can attribute novel properties onto intercalated compounds. Intercalating oxybenzone, a UV filter, within the interlamellar space of montmorillonite is desirable in order to minimize direct contact with skin. Intercalating resveratrol, a compound known for attributing beneficial effects onto human health, may be advantageous since this compound is susceptible to cis-trans isomerisation. The strategy of using alkylammonium--modified clay was undertaken and proved successful for the intercalation of oxybenzone. The field of biopolymer/layered silicate nanocomposites is heavily researched for use in a multitude of applications. Novel montmorillonite nanocomposites were prepared with neutral guar gum and cationic guar gum, using an environmentally friendly process and are fully characterized.

  10. Surface composition XPS analysis of a plasma treated polystyrene: Evolution over long storage periods.

    PubMed

    Ba, Ousmane M; Marmey, Pascal; Anselme, Karine; Duncan, Anthony C; Ponche, Arnaud

    2016-09-01

    A polystyrene surface (PS) was initially treated by cold nitrogen and oxygen plasma in order to incorporate in particular amine and hydroxyl functions, respectively. The evolution of the chemical nature of the surface was further monitored over a long time period (580 days) by chemical assay, XPS and contact angle measurements. Surface density quantification of primary amine groups was performed using three chemical amine assays: 4-nitrobenzaldehyde (4-NBZ), Sulfo succinimidyl 6-[3'(2 pyridyldithio)-pionamido] hexanoate (Sulfo-LC-SPDP) and iminothiolane (ITL). The results showed amine densities were in the range of 2 per square nanometer (comparable to the results described in the literature) after 5min of nitrogen plasma treatment. Over the time period investigated, chemical assays, XPS and contact angles suggest a drastic significant evolution of the chemical nature of the surface within the first two weeks. Beyond that time period and up to almost two years, nitrogen plasma modified substrates exhibits a slow and continuous oxidation whereas oxygen plasma modifed polystyrene surface is chemically stable after two weeks of storage. The latter appeared to "ease of" showing relatively mild changes within the one year period. Our results suggest that it may be preferable to wait for a chemical "stabilization" period of two weeks before subsequent covalent immobilization of proteins onto the surface. The originality of this work resides in the study of the plasma treated surface chemistry evolution over long periods of storage time (580 days) considerably exceeding those described in the literature. PMID:27131091

  11. In vitro attachment of osteoblasts on contaminated rough titanium surfaces treated by Er:YAG laser.

    PubMed

    Friedmann, Anton; Antic, Lilly; Bernimoulin, Jean-Pierre; Purucker, Peter

    2006-10-01

    Microbial contamination of implant surfaces inhibits formation of new osseous tissues. Biocompatibility of sandblasted large grid (SLA) surface, after previous in vitro cocultivation with Porphyromonas gingivalis and concomitant Er:YAG laser irradiation of microorganisms, was tested by attachment of newly cultured osteoblasts. A total of 36 customized titanium cubes with SLA surface were placed into human osteoblast culture for 14 days. After removal of 1 control cube, 35 other cubes were contaminated with precultured P. gingivalis (ATCC33277) and incubated in broth medium for 1 week. Ablation was carried out on 32 cubes. Each side was treated for 23.5 s with a pulsed, water-cooled laser beam. After irradiation, cubes were again placed into fresh osteoblast culture for 2 weeks. One randomly selected single side per cube was analyzed by scanning electron microscope in 22 cubes. On other 10 cubes, vitality of attached cells was tested with ethidiumbromide staining by fluorescence microscopy. Three negative controls revealed constantly adherent P. gingivalis, and no osteoblasts were detectable after P. gingivalis contamination on the surfaces. Laser-treated specimens showed newly attached osteoblasts, extending over 50-80% of the surface. Positive control cube (without bacterial contamination) showed over 80% cell coverage of the surface. Vitality of widely stretched osteoblasts was confirmed by FITC staining. Our results indicate that Er:YAG laser was effective in removing P. gingivalis and cell compounds, offering an acceptable surface for new osteoblast attachment. PMID:16758451

  12. Electric birefringence spectroscopy of montmorillonite particles.

    PubMed

    Arenas-Guerrero, Paloma; Iglesias, Guillermo R; Delgado, Ángel V; Jiménez, María L

    2016-06-14

    Electric birefringence (EB) of suspensions of anisotropic particles can be considered an electrokinetic phenomenon in a wide sense, as both liquid motions and polarization of the electrical double layer (EDL) of the particles participate in the process of particle orientation under the applied field. The EB spectrum can be exploited for obtaining information on the dimensions, average value and anisotropy of the surface conductivity of the particles, and the concentration and Maxwell-Wagner polarization of the EDLs. It is thus a highly informative technique, applicable to non-spherical particles. In this paper, we investigate the birefringent response of plate-like montmorillonite particles as a function of the frequency and amplitude of the applied AC electric field, for different compositions (pH, ionic strength, particle concentration) of the suspensions. The transient electric birefringence (i.e., the decay of the refractive index anisotropy with time when the field is switched off) is used for estimating the average dimensions of the particle axes, by modeling it as an oblate spheroid. The obtained values are very similar to those deduced from electron microscopy determinations. The frequency spectra show a very distinct behaviour at low (on the order of a few Hz) and high (up to several MHz) frequencies: the α and Maxwell-Wagner-O'Konski relaxations, characteristic of EDLs, are detected at frequencies above 10 kHz, and they can be well explained using electrokinetic models for the polarization of EDLs. At low frequencies, in contrast, the birefringence changes to negative, an anomalous response meaning that the particles tend to orient with their symmetry axis parallel to the field. This anomaly is weaker at basic pH values, high ionic strengths and low concentrations. The results can be explained by considering the polydispersity of real samples: the fastest particles redistribute around the slowest ones, inducing a hydrodynamic torque opposite to that of

  13. Adsorption of aniline and toluidines on montmorillonite

    SciTech Connect

    Essington, M.E. )

    1994-09-01

    Bentonite clay liners are commonly employed to mitigate the movement of contaminants from waste disposal sites. In order to assess the ability of clay liner material to restrict the mobility of amine compounds under a variety of chemical conditions and to further elucidate amine adsorption characteristics, the adsorption of aniline and o-, m-, and p-toluidine on Ca[sup 2+]- and K[sup +]-saturated Wyoming bentonite (SWy-1) was investigated. Adsorption experiments were performed under conditions of varied pH and ionic environment. Amine adsorption on montmorillonite is pH dependent. Maximum amine adsorption occurs when solution pH is approximately equal to the pK[sub a] of the anilinium ion deprotonation reaction (pH 4.45-5.08). An amine adsorption envelope results from the combined influence of increasing anilinium ion and anilinium-aniline complex formation (as pH decreases to the pK[sub a]) and amine competition with H[sup +] for surface sites, decreasing anilinium-aniline complex concentration, and decreasing aniline available for water bridging with exchangeable Ca[sup 2+] and K[sup +] (as solution pH decreases below the pK[sub a]). For any given amine, maximum adsorption increases with decreasing ionic strength. Maximum amine adsorption is greater in the Ca[sup 2+] systems than in the K[sup +] systems at equivalent cation charge and reflects the formation of an amine water bridge with the exchangeable Ca[sup 2+]. Amine adsorption is also greater in chloride systems compared with sulfate systems at comparable cation concentrations, possibly due to the formation of aqueous anilinium-sulfate complexes. The amine compounds are retained mainly by bentonite through a cation exchange process, the capacity of the clay to adsorb the amine compounds being a significant percentage of the exchange capacity at the pK[sub a]. However, amine retention decreases with increasing pH and is minimal at solution pH values greater than 7. 19 refs., 6 figs.

  14. Structural analysis of heat-treated birch (Betule papyrifera) surface during artificial weathering

    NASA Astrophysics Data System (ADS)

    Huang, Xianai; Kocaefe, Duygu; Kocaefe, Yasar; Boluk, Yaman; Krause, Cornélia

    2013-01-01

    Effect of artificial weathering on the surface structural changes of birch (Betule papyrifera) wood, heat-treated to different temperatures, was studied using the fluorescence microscopy and the scanning electron microscopy (SEM). Changes in the chemical structure of wood components were analyzed by FTIR in order to understand the mechanism of degradation taking place due to heat treatment and artificial weathering. The results are compared with those of the untreated (kiln-dried) birch. The SEM analysis results show that the effect of weathering on the cell wall of the untreated birch surface is more than that of heat-treated samples. The FTIR spectroscopy results indicate that lignin is the most sensitive component of heat-treated birch to the weathering degradation process. Elimination of the amorphous and highly crystallised cellulose is observed for both heat-treated and untreated wood during weathering. It is also observed that heat treatment increases the lignin and crystallised cellulose contents, which to some extent protects heat-treated birch against degradation due to weathering.

  15. Laser restoring the glass surface treated with acid-based paint

    NASA Astrophysics Data System (ADS)

    Strusevich, Anastasia V.; Poltaev, Yuriy A.; Sinev, Dmitrii A.

    2013-11-01

    The modern city facilities are often being attacked by graffiti artists, and increasingly vandals leave "tags" using paints, which compound based on acids, hydrofluoric or acetic commonly. These paints not only ink the surface, but also increase the surface roughness, and such impact can not be corrected by conventional cleaning. Thus, it was requested to develop technology that would not only clean the surface, but also to restore its structure by smoothing out irregularities and roughness formed after exposure in acid. In this work we investigated the effect of restoring the surface of the glass, spoiled by acid-based paint and then treated with CO2-laser. During the experiments, it was found that it is real to create the single-step laser surface restoring technology.

  16. X-ray photoelectron spectroscopic studies of carbon fiber surfaces. 22. Comparison between surface treatment of untreated and previously surface-treated fibers

    SciTech Connect

    Wang, Y.Q.; Viswanathan, H.; Audi, A.A.; Sherwood, P.M.A.

    2000-04-01

    IM7 PAN-based carbon fibers, with a proprietary surface treatment applied by the manufacturer, were analyzed by X-ray photoelectron spectroscopy (XPS). The surface treatment applied by the manufacturer was removed by heating in a vacuum. The fibers detreated in this manner were then subjected to electrochemical treatment. The electrochemical behavior of the as-received fibers and detreated fibers were measured and analyzed. When the same electrochemical treatment was applied to the as-received fibers with their commercial surface treatment intact, a different surface chemistry was observed for the detreated fibers. This study shows that the surface chemistry of treated fibers depends closely on the initial surface chemistry of the fibers and its detreatment. This work shows the importance of using untreated or detreated fibers as precursors for applying reproducible surface treatment so that one can understand and control the surface chemistry of fibers and their interfacial interaction in composites.

  17. Chemical surface modification of calcium carbonate particles with stearic acid using different treating methods

    NASA Astrophysics Data System (ADS)

    Cao, Zhi; Daly, Michael; Clémence, Lopez; Geever, Luke M.; Major, Ian; Higginbotham, Clement L.; Devine, Declan M.

    2016-08-01

    Calcium carbonate (CaCO3) is often treated with stearic acid (SA) to decrease its polarity. However, the method of application of the SA treatments has a strong influence on CaCO3 thermoplastic composite's interfacial structure and distribution. Several of papers describe the promising effects of SA surface treatment, but few compare the treatment process and its effect on the properties of the final thermoplastic composite. In the current study, we assessed a new SA treatment method, namely, complex treatment for polymer composite fabrication with HDPE. Subsequently, a comparative study was performed between the "complex" process and the other existing methods. The composites were assessed using different experiments included scanning electron microscopy (SEM), void content, density, wettability, differential scanning calorimetry (DSC), and tensile tests. It was observed that the "complex" surface treatment yielded composites with a significantly lower voids content and higher density compared to other surface treatments. This indicates that after the "complex" treatment process, the CaCO3 particles and HDPE matrix are more tightly packed than other methods. DSC and wettability results suggest that the "wet" and "complex" treated CaCO3 composites had a significantly higher heat of fusion and moisture resistance compared to the "dry" treated CaCO3 composites. Furthermore, "wet" and "complex" treated CaCO3 composites have a significantly higher tensile strength than the composites containing untreated and "dry" treated CaCO3. This is mainly because the "wet" and "complex" treatment processes have increased adsorption density of stearate, which enhances the interfacial interaction between matrix and filler. These results confirm that the chemical adsorption of the surfactant ions at the solid-liquid interface is higher than at other interface. From this study, it was concluded that the utilization of the "complex" method minimised the negative effects of void

  18. Surface roughness and color characteristics of wood treated with preservatives after accelerated weathering test

    NASA Astrophysics Data System (ADS)

    Temiz, Ali; Yildiz, Umit C.; Aydin, Ismail; Eikenes, Morten; Alfredsen, Gry; Çolakoglu, Gürsel

    2005-08-01

    Wood samples treated with ammonium copper quat (ACQ 1900 and ACQ 2200), chromated copper arsenate (CCA), Tanalith E 3491 and Wolmanit CX-8 have been studied in accelerated weathering experiments. The weathering experiment was performed by cycles of 2 h UV-light irradiation followed by water spray for 18 min. The changes on the surface of the weathered samples were characterized by roughness and color measurements on the samples with 0, 200, 400 and 600 h of total weathering. The objective of this study was to investigate the changes created by weathering on impregnated wood with several different wood preservatives. This study was performed on the accelerated weathering test cycle, using UV irradiation and water spray in order to simulate natural weathering. Surface roughness and color measurement was used to investigate the changes after several intervals (0-200-400-600 h) in artificial weathering of treated and untreated wood.

  19. Neptunium(V) sorption behavior on clinoptilolite, quartz and montmorillonite

    SciTech Connect

    Bertetti, F.P.; Pabalan, R.T.; Turner, D.R.; Almendarez, M.G.

    1996-08-01

    Performance assessment models have identified {sup 237}Np as a radionuclide of concern in meeting release limits established for the geologic disposal of high-level nuclear waste at the proposed repository at Yucca Mountain, Nevada. In this study, quartz, clinoptilolite, and montmorillonite, which are minerals representative of phases that occur both in the rock matrix and as fracture coatings at Yucca Mountain, were reacted with {sup 237}Np-bearing solutions to characterize the sorption behavior of Np(V) on these minerals. Batch experiments were conducted over a wide range of conditions in which pH of solution, surface loading, sorbent surface area, initial concentration of Np(V), and partial pressure of CO{sub 2} were varied. Initial Np(V) concentrations were between 1 {times} 10{sup {minus}7} and 1 {times} 10{sup {minus}6} M in electrolyte solutions of 0.1 or 0.01 M NaNO{sub 3}. The oxidation state of Np in solution was verified with NIR spectroscopy and by solvent extraction. Prior to the start of experiments, minerals were pretreated to eliminate impurities, and the clinoptilolite and montmorillonite were converted to Na-form by ion exchange with NaCl solutions. Results indicate that, for all three minerals, Np(V) sorption begins at pH values coincident with the start of hydrolysis in solution ({approximately}7). For solutions undersaturated with respect to atmospheric CO{sub 2}, sorption increases continuously with increasing pH. Under equilibrium with atmospheric CO{sub 2}, Np(V) sorption is important in the pH range (7--9.5) where NpO{sub 2}(OH){sup 0}(aq) is significant, whereas sorption is inhibited at higher pH where neptunyl carbonate complexes are the predominant species.

  20. Deposition of cobalt on surface-treated stainless steel under PWR conditions

    SciTech Connect

    Lister, D.H.; Anderson, P.G.; Barry, B.J.; Lavoie, R.G. . Chalk River Nuclear Labs.)

    1989-10-01

    As part of an on-going program aimed at reducing radiation exposures in light water reactors, the modification of surfaces to minimize their propensity to pick up radioactivity under reactor conditions has been studied. This report describes how stainless steel specimens, surface-treated with a variety of processes, picked up Co-60 from high-temperature water under PWR conditions in a high-pressure loop. The build-up of activity was monitored on-line with a movable gamma spectrometer. Off-line counting at the end of the experiment established the absolute activity levels, and selective examinations with SEM and metallography characterized the surface condition of the exceptional specimens. The effectiveness of the surface treatments was gauged by fitting simple parabolae to the activity build-up data and comparing the coefficients with those obtained from untreated control specimens. 10 refs., 23 figs., 4 tabs.

  1. Roughness modification of surfaces treated by a pulsed dielectric barrier discharge

    NASA Astrophysics Data System (ADS)

    Dumitrascu, N.; Borcia, G.; Apetroaei, N.; Popa, G.

    2002-05-01

    Local modifications of surface roughness are very important in many applications, as this surface property is able to generate new mechano-physical characteristics of a large category of materials. Roughness is one of the most important parameters used to characterize and control the surface morphology, and techniques that allow modifying and controlling the surface roughness present increasing interest. In this respect we propose the dielectric barrier discharge (DBD) as a simple and low cost method that can be used to induce controlled roughness on various surfaces in the nanoscale range. DBD is produced in helium, at atmospheric pressure, by a pulsed high voltage, 28 kV peak to peak, 13.5 kHz frequency and 40 W power. This type of discharge is a source of energy capable of modifying the physico-chemical properties of the surfaces without affecting their bulk properties. The discharge is characterized by means of electrical probes and, in order to analyse the heat transfer rate from the discharge to the treated surface, measurements of temperature distribution on the surface are performed. Influence of DBD on the roughness of surfaces with various properties, a semiconductor (tin oxide), a dielectric (polyvinylchloride) and a metallic (silver) surface, respectively, are investigated. Modifications of the surface morphology are detected by atomic force microscopy images, statistic roughness parameters and contact angle measurements. Results show an important increase of roughness and porosity of the thin films after DBD treatment, depending on the type of the material (semiconductor, dielectric and metallic). In the case of dielectric surfaces, this new morphology is correlated with adhesion work estimations. DBD treatments should be a convenient tool to induce a controlled roughness of various types of materials.

  2. Effectiveness of activated carbon and Egyptian montmorillonite in the protection against deoxynivalenol-induced cytotoxicity and genotoxicity in rats.

    PubMed

    Abdel-Wahhab, Mosaad A; El-Kady, Ahmed A; Hassan, Aziza M; Abd El-Moneim, Omaima M; Abdel-Aziem, Sekena H

    2015-09-01

    This study was conducted to prepare and characterize activated carbon (AC) and to evaluate its protective effect against deoxynivalenol (DON) toxicity in rats compared to Egyptian montmorillonite (EM). AC was prepared using a single-step chemical activation with phosphoric acid (H3PO4). The resulted AC has a high surface area and a high total pore volume. Male Sprague-Dawley rats were divided into 6 groups (n = 10) and treated for 3 weeks as follow: the control group, the groups fed AC or EM-supplemented diet (0.5% w/w), the group treated orally with DON (5 mg/kg b.w.) and the groups fed AC or EM-supplemented diet and treated with DON. Blood and liver samples were collected for different analyses. Treatment with DON increased liver function enzymes, lipid peroxidation, tumor necrosis factor α, DNA fragmentation, decreased hepatic glutathione content, up regulating mRNA Fas and TNF-α genes expression and increased micronucleated polychromatic erythrocytes and normochromatic erythrocytes in bone marrow. Co-treatment of DON plus AC or EM succeeded to normalize the levels of the biochemical parameters, reduced the cytotoxicity of bone marrow and ameliorated the hepatic genotoxicity. Moreover, AC was more effective than EM and has a high affinity to adsorb DON and to reduce its cytotoxicity and genotoxicity. PMID:26115597

  3. The long-term management of patients with tooth surface loss treated using removable appliances.

    PubMed

    Packer, M E; Davis, D M

    2000-11-01

    The causes of tooth surface loss are multi-factorial and hence can be difficult to eradicate. This paper identifies the problems that may be anticipated during the long-term management of patients where tooth surface loss has been treated using removable appliances, where the number of teeth is often reduced. Wear and tear are inevitable and patients should therefore be made fully aware of the possibility of the gradual deterioration and failure of restorative work. Treatments should be planned, which would enable the dentist to recover the situation, with minimal inconvenience to the patient. PMID:11218599

  4. Dislodgeable copper, chromium and arsenic from CCA-treated wood surfaces.

    PubMed

    Stilwell, David; Toner, Michael; Sawhney, Brij

    2003-08-01

    Chromated copper arsenate (CCA) is commonly used to preserve wood, but its use poses risk of arsenic exposure. In order to evaluate the extent of exposure to As from physical contact with CCA-treated wood, dislodgeable As from treated wood surfaces (as well as Cu and Cr) was determined as a function of weathering time using dampened polyester wipe materials. Six sets of 2.5-m-long CCA-treated boards, three-four boards per set, were purchased from lumber yards and cut into 30- or 60-cm coupons. A total of 44 such coupons were placed outdoors and the dislodgeable CCA components from the surfaces of the wooden coupons were periodically determined over a 1- or 2-year period by a systematic wipe method followed by nitric acid extraction of the CCA components from the cloth. In all 316 samples, appreciable amounts of the three elements, Cu, Cr and As, were detected. The amounts of surface-dislodgeable As, the most potentially hazardous element and the one of major concern in this study, varied from 5 to 122 microg/100 cm(2) with an average value of 37+/-22 microg/100 cm(2). There was considerable variation in As dislodged among coupons, boards, sets and time. Test coupons that tended to release relatively higher (or lower amounts) over time initially, continued to do so over time. However, the amounts of arsenic dislodged over time did not follow a simple pattern. While the As dislodged tended to decrease with time during the first year, it approached the initial value or increased somewhat during the second year, presumably due to surface rejuvenation effects caused by erosion and weathering. When all the data were normalized to the initial values, no trend emerged, as indicated by the average normalized value of 1.0+/-0.4 for As dislodged over time. Apparently, on installations constructed with CCA-treated wood, arsenic may remain available for a number of years. PMID:12873405

  5. Preparation and characterization of microporous SiO{sub 2}-ZrO{sub 2} pillared montmorillonite

    SciTech Connect

    Han, Yang-Su . E-mail: yshan@inanospace.com; Yamanaka, Shoji

    2006-04-15

    SiO{sub 2}-ZrO{sub 2} pillared montmorillonite (SZM) was prepared by the reaction of Na-montmorillonite with colloidal silica-zirconia particles which were prepared by depositing zirconium hydroxy cations on silica particles. By pillaring with the colloidal particles, the basal spacing of montmorillonite was expanded to ca. 45 A and the calcined SZM samples showed large specific surface areas up to 320 m{sup 2}/g at 400 deg. C. In spite of large interlayer separation, adsorption results indicated the presence of micropores generated between the colloidal particles. The microporous structure was maintained at least up to 600 deg. C and exhibited specific shape selectivity for the adsorption of large organic molecules, especially between toluene and mesitylene. According to the temperature-programmed-desorption (TPD) spectra of ammonia, the calcined SZM showed weakly acidic sites.

  6. Constructing covalent interface in rubber/clay nanocomposite by combining structural modification and interlamellar silylation of montmorillonite.

    PubMed

    Zha, Chao; Wang, Wencai; Lu, Yonglai; Zhang, Liqun

    2014-11-12

    Strong interfacial interaction and nanodispersion are necessary for polymer nanocomposites with expectations on mechanical performance. In this work, montmorillonite (MMT) was first structurally modified by acid treatment to produce more silanol groups on the layer surface. This was followed by chemical modification of γ-methacryloxy propyl trimethoxysilane molecule (KH570) through covalent grafting with the silanol groups. (29)Si and (27)Al magic angle spinning (MAS) NMR results revealed the microstructural changes of MMT after acid treatment and confirmed the increase of silanol groups on acid-treated MMT surfaces. Thermogravimetric analysis indicated an increase in the grafted amount of organosilane on the MMT surface. X-ray diffraction (XRD) showed that the functionalization process changed the highly ordered stacking structure of the MMT mineral into a highly disordered structure, indicating successful grafting of organosilane to the interlayer surface of the crystalline sheets. The styrene-butadiene rubber (SBR)/MMT nanocomposites were further prepared by co-coagulating with SBR latex and grafted-MMT aqueous suspension. During vulcanization, a covalent interface between modified MMT and rubber was established through peroxide-radical-initiated reactions, and layer aggregation was effectively prevented. The SBR/MMT nanocomposites had highly and uniformly dispersed MMT layers, and the covalent interfacial interaction was finally achieved and exhibited high performance. PMID:25322875

  7. Influence of montmorillonites exchange capacity on the basal spacing of cation–anion organo-montmorillonites

    SciTech Connect

    Sanqin, Wu; Zepeng, Zhang; Yunhua, Wang; Libing, Liao; Jiansheng, Zhang

    2014-11-15

    Graphical abstract: This picture shows the distribution of organic modifier (CTAB and SDS) in Mt interlayer and the basal spacing changes of Mt modified by CTAB and SDS. Organic modifier molecule in Mt interlayer is more and more orderly. The basal spacing of Mt is from 1.5 nm to 5 nm as modifier added. - Highlights: • The d{sub 001} of Ca-Mt, R-Na-Mt, Na-Mt modified by CTAB and SDS can reach 5 nm. • It is easier to get cation–anion OMt with greater d{sub 001} if CEC is lower. • The organic molecules distribution in cation–anion OMt was analyzed. • The influence mechanism of Ca-Mt CEC on the d{sub 001} was discussed. - Abstract: With cationic and anionic surfactants cetyltrimethylammonium bromide (CTAB) and sodium dodecylsulfonate (SDS) as modifiers, Ca-montmorillonites (Ca-Mt), artificial Na-montmorillonites (R-Na-Mt) and natural Na-montmorillonites (Na-Mt) with different cation exchange capacity (CEC) were modified by solution intercalation method, respectively. Then cation–anion organo-montmorillonites (OMt) were prepared. The influence of CEC on the basal spacing of cation–anion OMt and the influence mechanism were discussed by X-ray diffraction (XRD) and zeta potential testing. The results indicate that the basal spacing of cation–anion OMt is related to CEC. For the same type montmorillonites, the basal spacing of cation–anion OMt decreases with the increase of CEC and it is easier to get cation–anion OMt with greater basal spacing when CEC is lower. Moreover, the CEC of Na-Mt has the greatest influence on the basal spacing of cation–anion OMt.

  8. Corrosion behavior of Al-surface-treated steels in liquid Pb?Bi in a pot

    NASA Astrophysics Data System (ADS)

    Kurata, Y.; Futakawa, M.; Saito, S.

    2004-12-01

    Corrosion tests were performed in oxygen-saturated liquid Pb-Bi at 450 °C and 550 °C in a pot for 3000 h for Al-surface-treated steels containing various levels of Cr contents. The Al surface treatments were achieved using a gas diffusion method and a melt dipping method. Al2O3, FeAl2 and AlCr2 produced by the gas diffusion method exhibited corrosion resistance to liquid Pb-Bi, while the surface layer produced by the melt dipping method suffered a severe corrosion attack. Fe4Al13 and Fe2Al5 produced by the melt dipping method disappeared during the corrosion test at 550 °C and only FeAl remained.

  9. Tribological Properties of Aluminum Alloy treated by Fine Particle Peening/DLC Hybrid Surface Modification

    NASA Astrophysics Data System (ADS)

    Amano, Y.; Nanbu, H.; Kameyama, Y.; Komotori, J.

    2010-06-01

    In order to improve the adhesiveness of the DLC coating, Fine Particle Peening (FPP) treatment was employed as pre-treatment of the DLC coating process. FPP treatment was performed using SiC shot particles, and then AA6061-T6 aluminum alloy was DLC-coated. A SiC-rich layer was formed around the surface of the aluminum alloy by the FPP treatment because small chips of shot particles were embedded into the substrate surface. Reciprocating sliding tests were conducted to measure the friction coefficients. While the DLC coated specimen without FPP treatment showed a sudden increase in friction coefficient at the early stage of the wear cycles, the FPP/DLC hybrid treated specimen maintained a low friction coefficient value during the test period. Further investigation revealed that the tribological properties of the substrate after the DLC coating were improved with an increase in the amount of Si at the surface.

  10. Prebiotic RNA Synthesis by Montmorillonite Catalysis

    NASA Astrophysics Data System (ADS)

    Jheeta, Sohan; Joshi, Prakash C.

    2014-08-01

    This review summarizes our recent findings on the role of mineral salts in prebiotic RNA synthesis, which is catalyzed by montmorillonite clay minerals. The clay minerals not only catalyze the synthesis of RNA but also facilitate homochiral selection. Preliminary data of these findings have been presented at the "Horizontal Gene Transfer and the Last Universal Common Ancestor (LUCA)" conference at the Open University, Milton Keynes, UK, 5-6 September 2013. The objective of this meeting was to recognize the significance of RNA in LUCA. We believe that the prebiotic RNA synthesis from its monomers must have been a simple process. As a first step, it may have required activation of the 5'-end of the mononucleotide with a leaving group, e.g., imidazole in our model reaction (Figure 1). Wide ranges of activating groups are produced from HCN under plausible prebiotic Earth conditions. The final step is clay mineral catalysis in the presence of mineral salts to facilitate selective production of functional RNA. Both the clay minerals and mineral salts would have been abundant on early Earth. We have demonstrated that while montmorillonite (pH 7) produced only dimers from its monomers in water, addition of sodium chloride (1 M) enhanced the chain length multifold, as detected by HPLC. The effect of monovalent cations on RNA synthesis was of the following order: Li+ > Na+ > K+. A similar effect was observed with the anions, enhancing catalysis in the following order: Cl- > Br- > I-. The montmorillonite-catalyzed RNA synthesis was not affected by hydrophobic or hydrophilic interactions. We thus show that prebiotic synthesis of RNA from its monomers was a simple process requiring only clay minerals and a small amount of salt.

  11. Prebiotic RNA Synthesis by Montmorillonite Catalysis

    PubMed Central

    Jheeta, Sohan; Joshi, Prakash C.

    2014-01-01

    This review summarizes our recent findings on the role of mineral salts in prebiotic RNA synthesis, which is catalyzed by montmorillonite clay minerals. The clay minerals not only catalyze the synthesis of RNA but also facilitate homochiral selection. Preliminary data of these findings have been presented at the “Horizontal Gene Transfer and the Last Universal Common Ancestor (LUCA)” conference at the Open University, Milton Keynes, UK, 5–6 September 2013. The objective of this meeting was to recognize the significance of RNA in LUCA. We believe that the prebiotic RNA synthesis from its monomers must have been a simple process. As a first step, it may have required activation of the 5'-end of the mononucleotide with a leaving group, e.g., imidazole in our model reaction (Figure 1). Wide ranges of activating groups are produced from HCN under plausible prebiotic Earth conditions. The final step is clay mineral catalysis in the presence of mineral salts to facilitate selective production of functional RNA. Both the clay minerals and mineral salts would have been abundant on early Earth. We have demonstrated that while montmorillonite (pH 7) produced only dimers from its monomers in water, addition of sodium chloride (1 M) enhanced the chain length multifold, as detected by HPLC. The effect of monovalent cations on RNA synthesis was of the following order: Li+ > Na+ > K+. A similar effect was observed with the anions, enhancing catalysis in the following order: Cl− > Br− > I−. The montmorillonite-catalyzed RNA synthesis was not affected by hydrophobic or hydrophilic interactions. We thus show that prebiotic synthesis of RNA from its monomers was a simple process requiring only clay minerals and a small amount of salt. PMID:25370375

  12. Surface properties of low alloy steel treated by plasma nitrocarburizing prior to laser quenching process

    NASA Astrophysics Data System (ADS)

    Wang, Y. X.; Yan, M. F.; Li, B.; Guo, L. X.; Zhang, C. S.; Zhang, Y. X.; Bai, B.; Chen, L.; Long, Z.; Li, R. W.

    2015-04-01

    Laser quenching (LQ) technique is used as a part of duplex treatments to improve the thickness and hardness of the surface layers of steels. The present study is to investigate the surface properties of low alloy steel treated by plasma nitrocarburizing (PNC) prior to a laser quenching process (PNC+LQ). The microstructure and properties of PNC+LQ layer determined are compared with those obtained by PNC and LQ processes. OM, XRD, SEM and EDS analyses are utilized for microstructure observation, phases identification, morphology observation and chemical composition detection, respectively. Microhardness tester and pin-on-disc tribometer are used to investigate the mechanical properties of the modified layers. Laser quenching of plasma nitrocarburized (PNC+LQ) steel results in much improved thickness and hardness of the modified layer in comparison with the PNC or LQ treated specimens. The mechanism is that the introduction of trace of nitrogen decreases the eutectoid point, that is, the transformation hardened region is enlarged under the same temperature distribution. Moreover, the layer treated by PNC+LQ process exhibits enhanced wear resistance, due to the lubrication effect and optimized impact toughness, which is contributed to the formation of oxide film consisting of low nitrogen compound (FeN0.076) and iron oxidation (mainly of Fe3O4).

  13. Effects of surface treating methods of high-strength carbon fibers on interfacial properties of epoxy resin matrix composite

    NASA Astrophysics Data System (ADS)

    Ma, Quansheng; Gu, Yizhuo; Li, Min; Wang, Shaokai; Zhang, Zuoguang

    2016-08-01

    This paper aims to study the effects of surface treating methods, including electrolysis of anodic oxidation, sizing and heat treatment at 200 °C, on physical and chemical properties of T700 grade high-strength carbon fiber GQ4522. The fiber surface roughness, surface energy and chemical properties were analyzed for different treated carbon fibers, using atom force microscopy, contact angle, Fourier transformed infrared and X-ray photoelectron spectroscopy, respectively. The results show that the adopted surface treating methods significantly affect surface roughness, surface energy and active chemical groups of the studied carbon fibers. Electrolysis and sizing can increase the roughness, surface energy and chemical groups on surface, while heat treatment leads to decreases in surface energy and chemical groups due to chemical reaction of sizing. Then, unidirectional epoxy 5228 matrix composite laminates were prepared using different treated GQ4522 fibers, and interlaminar shear strength and flexural property were measured. It is revealed that the composite using electrolysis and sizing-fiber has the strongest interfacial bonding strength, indicating the important roles of the two treating processes on interfacial adhesion. Moreover, the composite using heat-treating fiber has lower mechanical properties, which is attributed to the decrease of chemical bonding between fiber surface and matrix after high temperature treatment of fiber.

  14. Hepatitis B surface antigen clearance in inactive hepatitis B surface antigen carriers treated with peginterferon alfa-2a

    PubMed Central

    Li, Ming-Hui; Xie, Yao; Zhang, Lu; Lu, Yao; Shen, Ge; Wu, Shu-Ling; Chang, Min; Mu, Cai-Qin; Hu, Lei-Ping; Hua, Wen-Hao; Song, Shu-Jing; Zhang, Shu-Feng; Cheng, Jun; Xu, Dao-Zhen

    2016-01-01

    AIM: To examine the association between interferon (IFN) therapy and loss of hepatitis B surface antigen (HBsAg) in inactive HBsAg carriers. METHODS: This was a retrospective cohort study in inactive HBsAg carriers, who were treatment-naive, with a serum HBsAg level < 100 IU/mL and an undetectable hepatitis B virus (HBV) DNA level (< 100 IU/mL). All the 20 treated patients received subcutaneous PEG-IFN alfa-2a 180 μg/wk for 72 wk and were then followed for 24 wk. There were 40 untreated controls matched with 96 wk of observation. Serum HBsAg, HBV DNA, and alanine aminotransferases were monitored every 3 mo in the treatment group and every 3-6 mo in the control group. RESULTS: Thirteen (65.0%) of 20 treated patients achieved HBsAg loss, 12 of whom achieved HBsAg seroconversion. Mean HBsAg level in treated patients decreased to 6.69 ± 13.04 IU/mL after 24 wk of treatment from a baseline level of 26.22 ± 33.00 IU/mL. Serum HBV DNA level remained undetectable (< 100 IU/mL) in all treated patients during the study. HBsAg level of the control group decreased from 25.72 ± 25.58 IU/mL at baseline to 17.11 ± 21.62 IU/mL at week 96 (P = 0.108). In the control group, no patient experienced HBsAg loss/seroconversion, and two (5.0%) developed HBV reactivation. CONCLUSION: IFN treatment results in HBsAg loss and seroconversion in a considerable proportion of inactive HBsAg carriers with low HBsAg concentrations. PMID:27239256

  15. Pedogenic formation of montmorillonite from a 2:1-2:2 intergrade clay mineral

    USGS Publications Warehouse

    Malcolm, R.L.; Nettleton, W.D.; McCracken, R.J.

    1969-01-01

    Montmorillonite was found to be the dominant clay mineral in surface horizons of certain soils of the North Carolina Coastal Plain whereas a 2:1-2:2 intergrade clay mineral was dominant in subjacent horizons. In all soils where this clay mineral sequence was found, the surface horizon was low in pH (below 4??5) and high in organic matter content. In contrast, data from studies of other soils of this region (Weed and Nelson, 1962) show that: (1) montmorillonite occurs infrequently; (2) maximum accumulation of the 2:1-2:2 intergrade normally occurs in the surface horizon and decreases with depth in the profile; (3) organic matter contents are low; and (4) pH values are only moderately acid (pH 5-6). It is theorized that the montmorillonite in the surface horizon of the soils studied originated by pedogenic weathering of the 2:1-2:2 intergrade clay mineral. The combined effects of low pH (below 4??5) and high organic matter content in surface horizons are believed to be the agents responsible for this mineral transformation. The protonation and solubilization (reverse of hydrolysis) of Al-polymers in the interlayer of expansible clay minerals will occur at or below pH 4??5 depending on the charge and steric effects of the interlayer. A low pH alone may cause this solubilization and thus mineral transformation, but in the soils studied the organic matter is believed to facilitate and accelerage the transformation. The intermediates of organic matter decomposition provide an acid environment, a source of protons, and a source of watersoluble mobile organic substances (principally fulvic acids) which have the ability to complex the solubilized aluminum and move it down the profile. This continuous removal of solubilized aluminum would provide for a favorable gradient for aluminum solubilization. The drainage class or position in a catena is believed to be less important than the chemical factors in formation of montmorillonite from 2:1-2:2 intergrade, because

  16. Characterization of Surface Treated Aero Engine Alloys by Rayleigh Wave Velocity Dispersion

    NASA Astrophysics Data System (ADS)

    Köhler, B.; Barth, M.; Schubert, F.; Bamberg, J.; Baron, H.-U.

    2010-02-01

    In aero engines mechanically high stressed components made of high-strength alloys like IN718 and Ti6Al4V are usually surface treated by shot-peening. Other methods, e.g. laser-peening, deep rolling and low plasticity burnishing are also available. All methods introduce compres-sive residual stress desired for minimize sensitivity to fatigue or stress corrosion failure mechanisms, resulting in improved performance and increased lifetime of components. Beside that, also cold work is introduced in an amount varying from method to method. To determine the remaining life time of critical aero engine components like compressor and turbine discs, a quantitative non-destructive determination of compressive stresses is required. The opportunity to estimate residual stress in surface treated aero engine alloys by SAW phase velocity measurements has been re-examined. For that original engine relevant material IN718 has been used. Contrary to other publications a significant effect of the surface treatment to the sound velocity was observed which disappeared after thermal treatment. Also preliminary measurements of the acousto-elastic coefficient fit into this picture.

  17. Osteoclasts but not osteoblasts are affected by a calcified surface treated with zoledronic acid in vitro

    SciTech Connect

    Schindeler, Aaron . E-mail: AaronS@chw.edu.au; Little, David G.

    2005-12-16

    Bisphosphonates are potent inhibitors of osteoclast-mediated bone resorption. Recent interest has centered on the effects of bisphosphonates on osteoblasts. Chronic dosing of osteoblasts with solubilized bisphosphonates has been reported to enhance osteogenesis and mineralization in vitro. However, this methodology poorly reflects the in vivo situation, where free bisphosphonate becomes rapidly bound to mineralized bone surfaces. To establish a more clinically relevant cell culture model, we cultured bone cells on calcium phosphate coated quartz discs pre-treated with the potent nitrogen-containing bisphosphonate, zoledronic acid (ZA). Binding studies utilizing [{sup 14}C]-labeled ZA confirmed that the bisphosphonate bound in a concentration-dependent manner over the 1-50 {mu}M dose range. When grown on ZA-treated discs, the viability of bone-marrow derived osteoclasts was greatly reduced, while the viability and mineralization of the osteoblastic MC3T3-E1 cell line were largely unaffected. This suggests that only bone resorbing cells are affected by bound bisphosphonate. However, this system does not account for transient exposure to unbound bisphosphonate in the hours following a clinical dosing. To model this event, we transiently treated osteoblasts with ZA in the absence of a calcified surface. Osteoblasts proved highly resistant to all transitory treatment regimes, even when utilizing ZA concentrations that prevented mineralization and/or induced cell death when dosed chronically. This study represents a pharmacologically more relevant approach to modeling bisphosphonate treatment on cultured bone cells and implies that bisphosphonate therapies may not directly affect osteoblasts at bone surfaces.

  18. Sorption/Desorption Interactions of Plutonium with Montmorillonite

    NASA Astrophysics Data System (ADS)

    Begg, J.; Zavarin, M.; Zhao, P.; Kersting, A. B.

    2012-12-01

    Plutonium (Pu) release to the environment through nuclear weapon development and the nuclear fuel cycle is an unfortunate legacy of the nuclear age. In part due to public health concerns over the risk of Pu contamination of drinking water, predicting the behavior of Pu in both surface and sub-surface water is a topic of continued interest. Typically it was assumed that Pu mobility in groundwater would be severely restricted, as laboratory adsorption studies commonly show that naturally occurring minerals can effectively remove plutonium from solution. However, evidence for the transport of Pu over significant distances at field sites highlights a relative lack of understanding of the fundamental processes controlling plutonium behavior in natural systems. At several field locations, enhanced mobility is due to Pu association with colloidal particles that serve to increase the transport of sorbed contaminants (Kersting et al., 1999; Santschi et al., 2002, Novikov et al., 2006). The ability for mineral colloids to transport Pu is in part controlled by its oxidation state and the rate of plutonium adsorption to, and desorption from, the mineral surface. Previously we have investigated the adsorption affinity of Pu for montmorillonite colloids, finding affinities to be similar over a wide range of Pu concentrations. In the present study we examine the stability of adsorbed Pu on the mineral surface. Pu(IV) at an initial concentration of 10-10 M was pre-equilibrated with montmorillonite in a background electrolyte at pH values of 4, 6 and 8. Following equilibration, aliquots of the suspensions were placed in a flow cell and Pu-free background electrolyte at the relevant pH was passed through the system. Flow rates were varied in order to investigate the kinetics of desorption and hence gain a mechanistic understanding of the desorption process. The flow cell experiments demonstrate that desorption of Pu from the montmorillonite surface cannot be modeled as a simple

  19. Effects of pH on dielectric relaxation of montmorillonite, allophane, and imogolite suspensions

    SciTech Connect

    Ishida, Tomoyuki; Makino, Tomoyuki

    1999-04-01

    Dielectric measurements were performed on montmorillonite, allophane, and imogolite suspensions under various pH conditions, using time domain reflectometry over the frequency range 10 kHz--20 GHz. A dielectric relaxation peak due to bound water could be observed for all the clays. Allophane has two peaks, indicating that its peaks are very similar to those of silica-alumina gels. Although imogolite has a similar chemical composition, only one peak was found. The relaxation strength of montmorillonite is greater than that of the other two clays. For all the clays, the relaxation strength depended on the pH. A change in the relaxation strength according to a change in pH is explained in terms of the different network structures of the clay particles. It is suggested that bound water influences the network structure formation. In montmorillonite, a great relaxation process detected at low frequency is caused by surface polarization of counterions. The change in measure of the structural unit with the pH, identified from Schwartz`s theory, has a tendency similar to that postulated by other experimental techniques, and surface charge densities identified are close to those estimated from CEC.

  20. Biocompatible, smooth, plasma-treated nickel-titanium surface--an adequate platform for cell growth.

    PubMed

    Chrzanowski, W; Szade, J; Hart, A D; Knowles, J C; Dalby, M J

    2012-02-01

    High nickel content is believed to reduce the number of biomedical applications of nickel-titanium alloy due to the reported toxicity of nickel. The reduction in nickel release and minimized exposure of the cell to nickel can optimize the biocompatibility of the alloy and increase its use in the application where its shape memory effects and pseudoelasticity are particularly useful, e.g., spinal implants. Many treatments have been tried to improve the biocompatibility of Ni-Ti, and results suggest that a native, smooth surface could provide sufficient tolerance, biologically. We hypothesized that the native surface of nickel-titanium supports cell differentiation and insures good biocompatibility. Three types of surface modifications were investigated: thermal oxidation, alkali treatment, and plasma sputtering, and compared with smooth, ground surface. Thermal oxidation caused a drop in surface nickel content, while negligible chemistry changes were observed for plasma-modified samples when compared with control ground samples. In contrast, alkali treatment caused significant increase in surface nickel concentration and accelerated nickel release. Nickel release was also accelerated in thermally oxidized samples at 600 °C, while in other samples it remained at low level. Both thermal oxidation and alkali treatment increased the roughness of the surface, but mean roughness R(a) was significantly greater for the alkali-treated ones. Ground and plasma-modified samples had 'smooth' surfaces with R(a)=4 nm. Deformability tests showed that the adhesion of the surface layers on samples oxidized at 600 °C and alkali treatment samples was not sufficient; the layer delaminated upon deformation. It was observed that the cell cytoskeletons on the samples with a high nickel content or release were less developed, suggesting some negative effects of nickel on cell growth. These effects were observed primarily during initial cell contact with the surface. The most favorable

  1. Microtensile bond strength and micromorphologic analysis of surface-treated resin nanoceramics

    PubMed Central

    Park, Joon-Ho

    2016-01-01

    PURPOSE The aim of this study was to evaluate the influence of different surface treatment methods on the microtensile bond strength of resin cement to resin nanoceramic (RNC). MATERIALS AND METHODS RNC onlays (Lava Ultimate) (n=30) were treated using air abrasion with and without a universal adhesive, or HF etching followed by a universal adhesive with and without a silane coupling agent, or tribological silica coating with and without a universal adhesive, and divided into 6 groups. Onlays were luted with resin cement to dentin surfaces. A microtensile bond strength test was performed and evaluated by one-way ANOVA and Tukey HSD test (α=.05). A nanoscratch test, field emission scanning electron microscopy, and energy dispersive X-ray spectroscopy were used for micromorphologic analysis (α=.05). The roughness and elemental proportion were evaluated by Kruskal–Wallis test and Mann–Whitney U test. RESULTS Tribological silica coating showed the highest roughness, followed by air abrasion and HF etching. After HF etching, the RNC surface presented a decrease in oxygen, silicon, and zirconium ratio with increasing carbon ratio. Air abrasion with universal adhesive showed the highest bond strength followed by tribological silica coating with universal adhesive. HF etching with universal adhesive showed the lowest bond strength. CONCLUSION An improved understanding of the effect of surface treatment of RNC could enhance the durability of resin bonding when used for indirect restorations. When using RNC for restoration, effective and systemic surface roughening methods and an appropriate adhesive are required. PMID:27555896

  2. Adhesion strength measurements of excimer-laser-treated PTFE surfaces using liquid photoreagents

    NASA Astrophysics Data System (ADS)

    Hopp, Bela; Smausz, Tomi; Kresz, Norbert; Ignacz, Ferenc

    2003-04-01

    The most known feature of polytetrafluoroethylene (PTFE) is its adhesion behavior: it is hydrophobic and oleophobic at the same time. This can cause serious problems and obstacles during the surface treatment and fixing of PTFE objects. During our experiments Teflon films were irradiated by an ArF excimer laser beam in presence of liquid photoreagents containing amine groups (aminoethanol, 1,2-diaminoethane, triethylene-tetramine). In consequence of the treatment the adhesion of the modified surfaces significantly increased, the samples could be glued and moistened. The adhesion strength of the glued surfaces was measured in the function of the applied laser fluence. The adhesion strength increased drastically between 0 - 1 mJ/cm2 and showed saturation above 1 mJ/cm2 at approximately 5 - 9 MPa values depending on the applied photoreagents. On the basis of our experiments it was found that the treatment with triethylene-tetramine was the most effective. The surface chemical modifications of the treated Teflon samples can be due to the incorporation of amine groups into the surface layer.

  3. Modification of the Steel Surface Treated by a Volume Discharge Plasma in Nitrogen at Atmospheric Pressure

    NASA Astrophysics Data System (ADS)

    Erofeev, M. V.; Shulepov, M. A.; Ivanov, Yu. F.; Oskomov, K. V.; Tarasenko, V. F.

    2016-03-01

    Effect of volume discharge plasma initiated by an avalanche electron beam on the composition, structure, and properties of the surface steel layer is investigated. Voltage pulses with incident wave amplitude up to 30 kV, full width at half maximum of about 4 ns, and wave front of about 2.5 ns were applied to the gap with an inhomogeneous electric field. Changes indicating the hardening effect of the volume discharge initiated by an avalanche electron beam are revealed in St3-grade steel specimens treated by the discharge of this type.

  4. Study of the influence of surface carbon on the tribological properties of ion-treated steels

    NASA Astrophysics Data System (ADS)

    Benyagoub, Abdenacer; Faussemagne, Arielle

    1999-01-01

    Samples of 100Cr6 steel were treated by different ion beams in order to study the evolution of their tribological properties. A strong correlation was found between the amount of surface carbon, whatever its origin (contamination, direct C implantation or ion-beam mixing of a deposited carbon layer), and the reduction of the friction coefficient as well as the improvement of the wear resistance. These results are discussed in the framework of a recent statistical model founded on the asperity concept and describing the tribological behaviour of bilayer systems.

  5. Aggregation of montmorillonite and organic matter in aqueous media containing artificial seawater

    PubMed Central

    2009-01-01

    Background The dispersion-aggregation behaviors of suspended colloids in rivers and estuaries are affected by the compositions of suspended materials (i.e., clay minerals vs. organic macromolecules) and salinity. Laboratory experiments were conducted to investigate the dispersion and aggregation mechanisms of suspended particles under simulated river and estuarine conditions. The average hydrodynamic diameters of suspended particles (representing degree of aggregation) and zeta potential (representing the electrokinetic properties of suspended colloids and aggregates) were determined for systems containing suspended montmorillonite, humic acid, and/or chitin at the circumneutral pH over a range of salinity (0 – 7.2 psu). Results The montmorillonite-only system increased the degree of aggregation with salinity increase, as would be expected for suspended colloids whose dispersion-aggregation behavior is largely controlled by the surface electrostatic properties and van der Waals forces. When montmorillonite is combined with humic acid or chitin, the aggregation of montmorillonite was effectively inhibited. The surface interaction energy model calculations reveal that the steric repulsion, rather than the increase in electronegativity, is the primary cause for the inhibition of aggregation by the addition of humic acid or chitin. Conclusion These results help explain the range of dispersion-aggregation behaviors observed in natural river and estuarine systems. It is postulated that the composition of suspended particles, specifically the availability of steric polymers such as those contained in humic acid, determine whether the river suspension is rapidly aggregated and settled or remains dispersed in suspension when it encounters increasingly saline environments of estuaries and oceans. PMID:19166595

  6. Surface and crystalline analysis of aluminum oxide single crystal treated by quasistationary compression plasma flow

    SciTech Connect

    Maletic, S.; Popovic, D.M.; Cubrovic, V.; Zekic, A.A.; Dojcilovic, J.

    2012-04-15

    Highlights: Black-Right-Pointing-Pointer The effects of treatment of Al{sub 2}O{sub 3} (0001) surface by CPF are analyzed. Black-Right-Pointing-Pointer Oriented low-dimensional structures are occurred for the treated Al{sub 2}O{sub 3} crystal. Black-Right-Pointing-Pointer The dimension of these ripples are 1 {mu}m and the distance between them is about 10 {mu}m. Black-Right-Pointing-Pointer The ripple-shaped structures contain a higher percentage of oxygen than the surroundings. Black-Right-Pointing-Pointer Results could promote CPF as a tool for producing organized oxygen-rich structures. -- Abstract: Material such as aluminum oxide (Al{sub 2}O{sub 3}) is important in electronics industry. On the other hand, plasma is one of the most efficient and sophisticated tools for materials processing. In this work a treatment of Al{sub 2}O{sub 3} (0001) surface by quasistationary compression plasma flow (CPF) is analyzed in detail. Offline metrology was performed using dielectric measurements, X-ray diffraction (XRD), scanning electron microscopy (SEM) equipped with energy-dispersive X-ray spectroscopy (EDX) and atomic force microscopy (AFM). Oriented low-dimensional periodic structures are occurred for the plasma treated Al{sub 2}O{sub 3} single crystal. In the paper is reported that these oriented ripple-shaped structures contain a higher percentage of oxygen than the surrounding crystal surface. This could be the framework for usage of CPF as a tool in manufacturing of surfaces containing the highly organized oxygen-rich structures.

  7. Adhesive forces and surface properties of cold gas plasma treated UHMWPE

    PubMed Central

    Preedy, Emily Callard; Brousseau, Emmanuel; Evans, Sam L.; Perni, Stefano; Prokopovich, Polina

    2014-01-01

    Cold atmospheric plasma (CAP) treatment was used on ultra-high molecular weight polyethylene (UHMWPE), a common articulating counter material employed in hip and knee replacements. UHMWPE is a biocompatible polymer with low friction coefficient, yet does not have robust wear characteristics. CAP effectively cross-links the polymer chains of the UHMWPE improving wear performance (Perni et al., Acta Biomater. 8(3) (2012) 1357). In this work, interactions between CAP treated UHMWPE and spherical borosilicate sphere (representing model material for bone) were considered employing AFM technique. Adhesive forces increased, in the presence of PBS, after treatment with helium and helium/oxygen cold gas plasmas. Furthermore, a more hydrophilic surface of UHMWPE was observed after both treatments, determined through a reduction of up to a third in the contact angles of water. On the other hand, the asperity density also decreased by half, yet the asperity height had a three-fold decrease. This work shows that CAP treatment can be a very effective technique at enhancing the adhesion between bone and UHMWPE implant material as aided by the increased adhesion forces. Moreover, the hydrophilicity of the CAP treated UHMWPE can lead to proteins and cells adhesion to the surface of the implant stimulating osseointegration process. PMID:25431523

  8. Adhesive forces and surface properties of cold gas plasma treated UHMWPE.

    PubMed

    Preedy, Emily Callard; Brousseau, Emmanuel; Evans, Sam L; Perni, Stefano; Prokopovich, Polina

    2014-10-20

    Cold atmospheric plasma (CAP) treatment was used on ultra-high molecular weight polyethylene (UHMWPE), a common articulating counter material employed in hip and knee replacements. UHMWPE is a biocompatible polymer with low friction coefficient, yet does not have robust wear characteristics. CAP effectively cross-links the polymer chains of the UHMWPE improving wear performance (Perni et al., Acta Biomater. 8(3) (2012) 1357). In this work, interactions between CAP treated UHMWPE and spherical borosilicate sphere (representing model material for bone) were considered employing AFM technique. Adhesive forces increased, in the presence of PBS, after treatment with helium and helium/oxygen cold gas plasmas. Furthermore, a more hydrophilic surface of UHMWPE was observed after both treatments, determined through a reduction of up to a third in the contact angles of water. On the other hand, the asperity density also decreased by half, yet the asperity height had a three-fold decrease. This work shows that CAP treatment can be a very effective technique at enhancing the adhesion between bone and UHMWPE implant material as aided by the increased adhesion forces. Moreover, the hydrophilicity of the CAP treated UHMWPE can lead to proteins and cells adhesion to the surface of the implant stimulating osseointegration process. PMID:25431523

  9. Effect of Surface Treated Silicon Dioxide Nanoparticles on Some Mechanical Properties of Maxillofacial Silicone Elastomer

    PubMed Central

    Zayed, Sara M.; Alshimy, Ahmad M.; Fahmy, Amal E.

    2014-01-01

    Current materials used for maxillofacial prostheses are far from ideal and there is a need for novel improved materials which mimic as close as possible the natural behavior of facial soft tissues. This study aimed to evaluate the effect of adding different concentrations of surface treated silicon dioxide nanoparticles (SiO2) on clinically important mechanical properties of a maxillofacial silicone elastomer. 147 specimens of the silicone elastomer were prepared and divided into seven groups (n = 21). One control group was prepared without nanoparticles and six study groups with different concentrations of nanoparticles, from 0.5% to 3% by weight. Specimens were tested for tear strength (ASTM D624), tensile strength (ASTM D412), percent elongation, and shore A hardness. SEM was used to assess the dispersion of nano-SiO2 within the elastomer matrix. Data were analyzed by one-way ANOVA and Scheffe test (α = 0.05). Results revealed significant improvement in all mechanical properties tested, as the concentration of the nanoparticles increased. This was supported by the results of the SEM. Hence, it can be concluded that the incorporation of surface treated SiO2 nanoparticles at concentration of 3% enhanced the overall mechanical properties of A-2186 silicone elastomer. PMID:25574170

  10. In vitro screening procedure for characterization of thrombogenic properties of plasma treated surfaces.

    PubMed

    Modic, Martina; Mozetič, Miran

    2016-01-01

    Estimation of thrombogenic surface properties is an important aspect of hemocompatibility studies. To improve our understanding of interaction between blood and biomaterial surfaces, there is a need to employ standardized methods that are both effective and efficient. This contribution details a systematic approach for the in vitro analysis of plasma modified polymer surfaces and human blood platelet interaction, following the recently introduced ISO 10933-4 guidelines. A holistic multistep process is presented that considers all aspects of testing procedure, including blood collection, platelet function testing, and incubation parameters, right through to a comparison and evaluation of the different methods and analysis available. In terms of detection and analysis, confocal light microscopy is shown to offer many advantages over the widely used scanning electron microscopy technique; this includes simpler, less-invasive sample preparation, and less time-consuming analysis procedure. On the other hand, as an alternative to microscopy techniques, toxicology sulforhodamine B based assay (TOX assay) was also evaluated. It has been shown that the assay could be used for rapid estimation of relative concentration of blood platelets on the surface of plasma treated materials, especially when samples do not allow the implementation of microscopy techniques. PMID:27154919

  11. Polymerization of serine guanylate in the presence of montmorillonite

    NASA Technical Reports Server (NTRS)

    Paecht-Horowitz, M.

    1981-01-01

    Serine guanylate was prepared and its polymerization studied in the presence of montmorillonite and in its absence. In water, without clay, serine guanylate polymerizes in the same way as does serine adenylate. In the presence of montmorillonite, serine guanylate polymerizes to a lesser extent and produces also lower degrees of polymerization than does serine adenylate. It is postulated that the reason for this difference in behavior might lie in the fact that guanylic acid is much more acidic than adenylic acid; hence would bind much more strongly to the edges of montmorillonite and thus, by blocking these sites, would inhibit the catalytic activity of the clay.

  12. Carbonate formation in Wyoming montmorillonite under high pressure carbon dioxide

    SciTech Connect

    Hur, Tae-Bong; Baltrus, John P.; Howard, Bret H.; Harbert, William P.; Romanov, Vyacheslav N.

    2013-03-01

    Carbonation reaction with silicate minerals that are common components of the host rock and cap rock within geological storage reservoirs and the associated structural deformation were investigated for better understanding of the geochemical reactions associated with geologic CO2 storage. Exposure of a model expanding clay, Wyoming montmorillonite, SWy-2, to high-pressure CO2 resulted in the formation of a mineral carbonate phase via dry CO2–clay mineral interactions at two different temperatures. The experimental evidence suggests that the properties of CO2 fluid at 70 °C provide more favorable conditions for carbonate formation at the clay surface less accessible to CO2 at 22 °C. The carbonation reaction occurred predominantly within the first couple of days of exposure to the fluid and then proceeded slower with continuing exposure. As compared to the as-received clay under the same ambient conditions, the (0 0 1) basal spacing of the clay bearing carbonates (after the CO2 exposure) was slightly expanded at a relative humidity (RH) level of 12% but it was slightly collapsed at the RH level of 40%. Finally, experimental observations suggest that the carbonation reaction occurs at the external surface as well as internal surface (interlayer) of the clay particles.

  13. Behavior of codling moth (Lepidoptera: Tortricidae) neonate larvae on surfaces treated with microencapsulated pear ester.

    PubMed

    Light, Douglas M; Beck, John J

    2012-06-01

    Codling moth, Cydia pomonella (L.), larvae cause severe internal feeding damage to apples, pears, and walnuts worldwide. Research has demonstrated that codling moth neonate first instar larvae are attracted to a pear-derived kairomone, ethyl (2E,4Z)-2,4-decadienoate, the pear ester (PE). Reported here are the behavioral activities of neonate codling moth larvae to microencapsulated pear ester (MEC-PE) applied in aqueous solutions to both filter paper and apple leaf surfaces that were evaluated over a period of up to 20 d of aging. In dual-choice tests the MEC-PE treatment elicited attraction to and longer time spent on treated zones of filter papers relative to water-treated control zones for up to 14 d of aging. A higher concentration of MEC-PE caused no preferential response to the treated zone for the first 5 d of aging followed by significant responses through day 20 of aging, suggesting sensory adaptation as an initial concentration factor. Estimated emission levels of PE from treated filter papers were experimentally calculated for the observed behavioral thresholds evident over the aging period. When applied to apple leaves, MEC-PE changed neonate walking behavior by eliciting more frequent and longer time periods of arrestment and affected their ability to find the leaf base and stem or petiole. Effects of MEC-PE on extended walking time and arrestment by codling moth larvae would increase temporal and spatial exposure of neonates while on leaves; thereby potentially disrupting fruit or nut finding and enhancing mortality by increasing the exposure to insecticides, predation, and abiotic factors. PMID:22732619

  14. High-Power Diode Laser Surface Treated HVOF Coating to Combat High Energy Particle Impact Wear

    NASA Astrophysics Data System (ADS)

    Mann, B. S.; Arya, Vivek; Pant, B. K.

    2013-07-01

    High-velocity oxy-fuel (HVOF)-sprayed coatings have performed exceptionally well in low-energy particle impact wear and are accepted worldwide. However, their application for high-energy particle impact wear (HEPIW) requires a different approach and more efforts. HVOF-coating systems typically use WC-Co, WC-Co-Cr, WC-Ni-Cr, and FeCrAlY-Cr3C2 powders. WC-Co-Cr powders are preferred when there is a high demand for corrosion resistance. WC-10Co-4Cr coating powder has been selected in the current study. To improve coating properties such as microhardness, fracture toughness, and HEPIW resistance, a new approach of surface treatment with robotically controlled high-power diode laser (HPDL) is attempted. The robotically controlled HVOF-coating deposition and laser surface treatment were monitored using real-time diagnostic control. The HPDL-treated coating has been compared with "as-sprayed" HVOF coating for HEPIW resistance, fracture toughness, microhardness and microstructure. The coating characteristics and properties after laser surface treatment have improved many times compared with "as-sprayed" HVOF coating. This is due to the elimination of pores in the coating and formation of a metallurgical bond between coating and substrate. This new development opens up a possibility of using such laser treatments in specialized areas where HEPIW damages are acute. The fracture toughness and HEPIW resistance along with optical micrographs of HPDL-treated and untreated HVOF coatings are discussed and reported in this article. HEPIW resistance is observed to be proportional to the product of fracture toughness and microhardness of the HVOF coating.

  15. Study of antibacterial activity of Ag and Ag2CO3 nanoparticles stabilized over montmorillonite

    NASA Astrophysics Data System (ADS)

    Sohrabnezhad, Sh.; Pourahmad, A.; Mehdipour Moghaddam, M. J.; Sadeghi, A.

    2015-02-01

    Silver carbonate and silver nanoparticles (NPs) over of stabilizer montmorillonite (MMT) have been synthesized in aqueous and polyol solvent, respectively. Dispersions of silver nanoparticles have been prepared by the reduction of silver nitrate over of MMT in presence and absence of Na2CO3 compound in ethylene glycol. It was observed that montmorillonite was capable of stabilizing formed Ag nanoparticles through the reduction of Ag+ ions in ethylene glycol. Na2CO3 was used as carbonate source in synthesis of Ag2CO3 NPs in water solvent and also for controlling of Ag nanoparticles size in ethylene glycol medium. The samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and ultraviolet-visible diffuse reflectance spectroscopy (DRS). The TEM images showed that Ag NPs size in presence Na2CO3 salts was smaller than without that. The results indicated intercalation of Ag and Ag2CO3 nanoparticles into the montmorillonite clay layers. The diffuse reflectance spectra exhibited a strong surface plasmon resonance (SPR) adsorption peak in the visible region, resulting from Ag nanoparticles. The antibacterial testing results showed that the Ag2CO3-MMT nanocomposite exhibited an antibacterial activity higher than Ag-MMT sample against Escherichia coli.

  16. Molecular dynamics simulation of diffusion and electrical conductivity in montmorillonite interlayers

    DOE PAGESBeta

    Greathouse, Jeffery A.; Cygan, Randall T.; Fredrich, Joanne T.; Jerauld, Gary R.

    2016-01-20

    In this study, the diffusion of water and ions in the interlayer region of smectite clay minerals represents a direct probe of the type and strength of clay–fluid interactions. Interlayer diffusion also represents an important link between molecular simulation and macroscopic experiments. Here we use molecular dynamics simulation to investigate trends in cation and water diffusion in montmorillonite interlayers, looking specifically at the effects of layer charge, interlayer cation and cation charge (sodium or calcium), water content, and temperature. For Na-montmorillonite, the largest increase in ion and water diffusion coefficients occurs between the one-layer and two-layer hydrates, corresponding to themore » transition from inner-sphere to outer-sphere surface complexes. Calculated activation energies for ion and water diffusion in Na-montmorillonite are similar to each other and to the water hydrogen bond energy, suggesting the breaking of water–water and water–clay hydrogen bonds as a likely mechanism for interlayer diffusion. A comparison of interlayer diffusion with that of bulk electrolyte solutions reveals a clear trend of decreasing diffusion coefficient with increasing electrolyte concentration, and in most cases the interlayer diffusion results are nearly coincident with the corresponding bulk solutions. Trends in electrical conductivities computed from the ion diffusion coefficients are also compared.« less

  17. Analysis of Oligonucleotide DNA Binding and Sedimentation Properties of Montmorillonite Clay Using Ultraviolet Light Spectroscopy

    PubMed Central

    Beall, Gary W.; Sowersby, Drew S.; Roberts, Rachel D.; Robson, Michael H.; Lewis, L. Kevin

    2009-01-01

    Smectite clays such as montmorillonite form complexes with a variety of biomolecules, including the nucleic acids DNA and RNA. Most previous studies of DNA adsorption onto clay have relied upon spectrophotometric analysis after separation of free nucleic acids from bound complexes by centrifugation. In the current work we demonstrate that such studies produce a consistent error due to (a) incomplete sedimentation of montmorillonite and (b) strong absorbance of the remaining clay at 260 nm. Clay sedimentation efficiency was strongly dependent upon cation concentration (Na+ or Mg2+) and on the level of dispersion of the original suspension. An improved clay:DNA adsorption assay was developed and utilized to assess the impact of metal counterions on binding of single-stranded DNA to montmorillonite. X-ray diffraction demonstrated, for the first time, formation of intercalated structures consistent with orientation of the DNA strands parallel to the clay surface. Observed gallery spacings were found to closely match values calculated utilizing atomistic modeling techniques. PMID:19061334

  18. Treatment of an automobile effluent from heavy metals contamination by an eco-friendly montmorillonite

    PubMed Central

    Akpomie, Kovo G.; Dawodu, Folasegun A.

    2014-01-01

    Unmodified montmorillonite clay was utilized as a low cost adsorbent for the removal of heavy metals from a contaminated automobile effluent. Fourier transform infrared spectroscopy, X-ray diffraction and scanning electron microscopy were used to characterize the adsorbent. Batch sorption experiments were performed at an optimum effluent pH of 6.5, adsorbent dose of 0.1 g, particle size of 100 μm and equilibrium contact time of 180 min. Thermodynamic analysis was also conducted. Equilibrium data were analyzed by the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich models. A heterogeneous surface of the adsorbent was indicated by the Freundlich model. The Langmuir maximum adsorption capacity of the montmorillonite for metals was found in the following order: Zn (5.7 mg/g) > Cu (1.58 mg/g) > Mn (0.59 mg/g) > Cd (0.33 mg/g) > Pb (0.10 mg/g) ≡ Ni (0.10 mg/g). This was directly related to the concentration of the metal ions in solution. The pseudo-first order, pseudo-second order, intraparticle diffusion and liquid film diffusion models were applied for kinetic analysis. The mechanism of sorption was found to be dominated by the film diffusion mechanism. The results of this study revealed the potential of the montmorillonite for treatment of heavy metal contaminated effluents. PMID:26644939

  19. Fe(II) uptake on natural montmorillonites. I. Macroscopic and spectroscopic characterization.

    PubMed

    Soltermann, Daniela; Marques Fernandes, Maria; Baeyens, Bart; Dähn, Rainer; Joshi, Prachi A; Scheinost, Andreas C; Gorski, Christopher A

    2014-01-01

    Iron is an important redox-active element that is ubiquitous in both engineered and natural environments. In this study, the retention mechanism of Fe(II) on clay minerals was investigated using macroscopic sorption experiments combined with Mössbauer and extended X-ray absorption fine structure (EXAFS) spectroscopy. Sorption edges and isotherms were measured under anoxic conditions on natural Fe-bearing montmorillonites (STx, SWy, and SWa) having different structural Fe contents ranging from 0.5 to 15.4 wt % and different initial Fe redox states. Batch experiments indicated that, in the case of low Fe-bearing (STx) and dithionite-reduced clays, the Fe(II) uptake follows the sorption behavior of other divalent transition metals, whereas Fe(II) sorption increased by up to 2 orders of magnitude on the unreduced, Fe(III)-rich montmorillonites (SWy and SWa). Mössbauer spectroscopy analysis revealed that nearly all the sorbed Fe(II) was oxidized to surface-bound Fe(III) and secondary Fe(III) precipitates were formed on the Fe(III)-rich montmorillonite, while sorbed Fe is predominantly present as Fe(II) on Fe-low and dithionite-reduced clays. The results provide compelling evidence that Fe(II) uptake characteristics on clay minerals are strongly correlated to the redox properties of the structural Fe(III). The improved understanding of the interfacial redox interactions between sorbed Fe(II) and clay minerals gained in this study is essential for future studies developing Fe(II) sorption models on natural montmorillonites. PMID:24930689

  20. Estimating Dermal Transfer of Copper Particles from the Surfaces of Pressure-Treated Lumber and Implications for Exposure

    EPA Science Inventory

    Lumber pressure-treated with micronized copper was examined for the release of copper and copper micro/nanoparticles using a surface wipe method to simulate dermal transfer. In 2003, the wood industry began replacing CCA treated lumber products for residential use with copper ba...

  1. Cuprous Ion Conducting Montmorillonite- Polypyrrole Nanocomposites

    NASA Astrophysics Data System (ADS)

    Krishantha, D. M. M.; Rajapakse, R. M. G.; Tennakoon, D. T. B.; Bandara, W. M. A. T.; Thilakarathna, P. N. L.

    2006-06-01

    Solid state polymer-Silicate nanocomposite based on Polypyrrole-Cu+-montmorilonite were prepared and electrical properties were investigated. In this preparation, Na-montmorillonite (Na+-MMT) was purified by repeated washing with distilled water and the intergallery cations were exchanged for Cu(II). The cupric ions exchanged-MMT(Cu(II)-- MMT) was again exposed to pyrrole in aqueous acidic solution to yield polypyrrole-Cu+-MMT nanocomposite. DC polarization test and AC impedance measurement reveal that the materials are mixed conductors. The ionic conductivity is due to the motion of cuprous ions which is facilitated by microstructure of polypyrrrole present in the intergalleries. An electrochemical cell was fabricated using the materials which can be represented by Cu(s)/ Cu+-PPY-MMT/Cu2SO4 (s)/Na2SO4(S)-Na2S2O8(s)/ and gave a 1.00 V. The cell is rechargeable.

  2. Pillared montmorillonite catalysts for coal liquefaction

    SciTech Connect

    Sharma, R.K.; Olson, E.S.

    1994-12-31

    Pillared clays contain large micropores and have considerable potential for catalytic hydrogenation and cleavage of coal macromolecules. Pillared montmorillonite-supported catalysts were prepared by the intercalation of polynuclear hydroxychromium cations and subsequent impregnation of nickel and molybdenum. Infrared and thermogravimetric studies of pyridine-adsorbed catalysts indicated the presence of both Lewis and Bronsted acid sites. Thus, the catalysts have both acidic properties that can aid in hydrocracking and cleavage of carbon-heteroatom bonds as well as hydrogen-activating bimetallic sites. These catalysts were applied to the hydrodesulfurization and liquefaction of coal-derived intermediates. The reactions of model organosulfur compounds and coal liquids were carried out at 300{degrees}-400{degrees}C for 3 hours in the presence of 1000 psi of molecular hydrogen. Reaction products were analyzed by GC/FT-IR/MS/AED. The catalysts have been found to be very effective in removing sulfur from model compounds as well as liquefaction products.

  3. Nontronite and Montmorillonite as Nutrient Sources for Life on Mars

    NASA Astrophysics Data System (ADS)

    Mickol, R. L.; Craig, P. I.; Kral, T. A.

    2016-05-01

    Methanogens were grown in media containing bicarbonate buffer, nontronite or montmorillonite clay, and hydrogen gas. No other nutrients were added. These results suggest that martian clays may provide adequate nutrients to support organism growth.

  4. Dissolution of alkaline earth sulfates in the presence of montmorillonite

    USGS Publications Warehouse

    Eberl, D.D.; Landa, E.R.

    1985-01-01

    In a study of the effect of montmorillonite on the dissolution of BaSO4 (barite), SrSO4 (celestite), and 226Ra from U mill tailings, it was found that: (1) More of these substances dissolve in an aqueous system that contains montmorillonite than dissolve in a similar system without clay, due to the ion exchange properties of the clay; (2) Na-montmorillonite is more effective in aiding dissolution than is Ca-montmorillonite; (3) the amount of Ra that moves from mill tailings to an exchanger increases as solution sulfate activity decreases. Leaching experiments suggest that 226Ra from H2SO4-circuit U mill tailings from Edgemont, South Dakota, is not present as pure Ra sulfate or as an impurity in anhydrite or gypsum; it is less soluble, and probably occurs as a trace constituent in barite.

  5. Insights into tetracycline adsorption onto kaolinite and montmorillonite: experiments and modeling.

    PubMed

    Zhao, Yanping; Gu, Xueyuan; Li, Shiyin; Han, Ruiming; Wang, Guoxiang

    2015-11-01

    Adsorption of tetracycline (TC) on kaolinite and montmorillonite was investigated using batch adsorption experiments with different pH, ionic strength, and surface coverage. As a result, pH and ionic strength-dependent adsorption of TC was observed for the two clay minerals. The adsorption of TC decreased with the increase of pH and ionic strength, and high initial TC concentration had high adsorption. In addition, a triple-layer model was used to predict the adsorption and surface speciation of TC on the two minerals. As a result, four complex species on kaolinite (≡X(-)∙H3TC(+), ≡X(-)∙H2TC(±), ≡SOH(0)∙H2TC(±), and ≡SOH(0)∙HTC(-)) and three species on montmorillonite (≡X(-)∙H3TC(+), ≡X(-)∙H2TC(±), and ≡SOH(0)∙HTC(-)) were structurally constrained by spectroscopy, and these species were also successfully fitted to the adsorption edges of TC. Three functional groups of TC were involved in these adsorption reactions, including the positively charged dimethylamino group, the C=O amide I group, and the C=O group at the C ring. Combining adsorption experiments and model in this study, the adsorption of TC on kaolinite and montmorillonite was mainly attributed to cation exchange on the surface sites (≡X(-)) compared to surface complexation on the edge sites (≡SOH) at natural soil pH condition. Moreover, the surface adsorption species, the corresponding adsorption modes, and the binding constants for the surface reactions were also estimated. PMID:26122570

  6. Montmorillonite-induced Bacteriophage φ6 Disassembly

    NASA Astrophysics Data System (ADS)

    Trusiak, A.; Gottlieb, P.; Katz, A.; Alimova, A.; Steiner, J. C.; Block, K. A.

    2012-12-01

    It is estimated that there are 1031 virus particles on Earth making viruses an order of magnitude more prevalent in number than prokaryotes with the vast majority of viruses being bacteriophages. Clays are a major component of soils and aquatic sediments and can react with RNA, proteins and bacterial biofilms. The clays in soils serve as an important moderator between phage and their host bacteria, helping to preserve the evolutionary balance. Studies on the effects of clays on viral infectivity have given somewhat contradictory results; possibly a consequence of clay-virus interactions being dependent on the unique structure of particular viruses. In this work, the interaction between montmorillonite and the bacteriophage φ6 is investigated. φ6 is a member of the cystovirus family that infects Pseudomonas syringe, a common plant pathogen. As a member of the cystovirus family with an enveloped structure, φ6 serves as a model for reoviruses, a human pathogen. Experiments were conducted with φ6 suspended in dilute, purified homoionic commercial-grade montmorillonite over a range of virus:clay ratios. At a 1:100000 virus:clay ratio, the clay reduced viral infectivity by 99%. The minimum clay to virus ratio which results in a measurable reduction of P. syringae infection is 1:1. Electron microscopy demonstrates that mixed suspensions of smectite and virus co-aggregate to form flocs encompassing virions within the smectite. Both free viral particles as well as those imbedded in the flocs are seen in the micrographs to be missing the envelope- leaving only the nucleocapsid (NC) intact; indicating that smectite inactivates the virus by envelope disassembly. These results have strong implications in the evolution of both the φ6 virus and its P. syringae host cells. TEM of aggregate showing several disassembled NCs.

  7. Montmorillonite-levan nanocomposites with improved thermal and mechanical properties.

    PubMed

    Chen, Xiaoming; Gao, Hongsheng; Ploehn, Harry J

    2014-01-30

    This work reports on the structure and properties of novel nanocomposites composed of exfoliated montmorillonite clay blended with levan, a polysaccharide produced by Bacillus sp. Dry levan is very brittle, making it difficult to obtain stand-alone films. MMT-levan composites were prepared by solution blending in water, coating on plastic surfaces, partial drying at 50°C, and conditioning in air at 50-60% relative humidity. This process results in freestanding, transparent, and flexible films of pure levan and MMT-levan composites plasticized by 10-15 wt% water. XRD patterns from levan-MMT composites indicate an MMT interlayer spacing 0.62 nm greater than that of the starting MMT, suggesting re-stacking of MMT platelets coated by adsorbed, uncoiled levan molecules. FTIR results suggest that levan adheres to MMT via water-mediated hydrogen bonding between the levan's hydroxyl groups and MMT surface oxygens. MMT-levan composites have improved thermal stability and a well-defined glass transition temperature that increases with MMT loading. The tensile moduli of levan-MMT composites increase by as much as 480% relative to pure levan. The XRD and mechanical property results suggest that MMT reinforces levan through a filler network structure composed of MMT platelets bridged by adsorbed levan molecules, enhanced when the MMT loading becomes high enough (5-10wt% MMT) to induce an isotropic-nematic transition in MMT platelet orientation. PMID:24299812

  8. Disassembly of the cystovirus ϕ6 envelope by montmorillonite clay.

    PubMed

    Block, Karin A; Trusiak, Adrianna; Katz, Al; Gottlieb, Paul; Alimova, Alexandra; Wei, Hui; Morales, Jorge; Rice, William J; Steiner, Jeffrey C

    2014-02-01

    Prior studies of clay-virus interactions have focused on the stability and infectivity of nonenveloped viruses, yielding contradictory results. We hypothesize that the surface charge distribution of the clay and virus envelope dictates how the components react and affect aggregation, viral stability, and infectivity. The bacteriophage Cystoviridae species φ6 used in this study is a good model for enveloped pathogens. The interaction between φ6 and montmorillonite (MMT) clay (the primary component of bentonite) is explored by transmission electron microscopy. The analyses show that MMT-φ6 mixtures undergo heteroaggregation, forming structures in which virtually all the virions are either sequestered between MMT platelet layers or attached to platelet edges. The virions swell and undergo disassembly resulting in partial or total envelope loss. Edge-attached viral envelopes distort to increase contact area with the positively charged platelet edges indicating that the virion surface is negatively charged. The nucleocapsid (NCs) remaining after envelope removal also exhibit distortion, in contrast to detergent-produced NCs which exhibit no distortion. This visually discernible disassembly is a mechanism for loss of infectivity previously unreported by studies of nonenveloped viruses. The MMT-mediated sequestration and disassembly result in reduced infectivity, suggesting that clays may reduce infectivity of enveloped pathogenic viruses in soils and sediments. PMID:24357622

  9. Disassembly of the cystovirus ϕ6 envelope by montmorillonite clay

    PubMed Central

    Block, Karin A; Trusiak, Adrianna; Katz, Al; Gottlieb, Paul; Alimova, Alexandra; Wei, Hui; Morales, Jorge; Rice, William J; Steiner, Jeffrey C

    2014-01-01

    Prior studies of clay–virus interactions have focused on the stability and infectivity of nonenveloped viruses, yielding contradictory results. We hypothesize that the surface charge distribution of the clay and virus envelope dictates how the components react and affect aggregation, viral stability, and infectivity. The bacteriophage Cystoviridae species φ6 used in this study is a good model for enveloped pathogens. The interaction between φ6 and montmorillonite (MMT) clay (the primary component of bentonite) is explored by transmission electron microscopy. The analyses show that MMT–φ6 mixtures undergo heteroaggregation, forming structures in which virtually all the virions are either sequestered between MMT platelet layers or attached to platelet edges. The virions swell and undergo disassembly resulting in partial or total envelope loss. Edge-attached viral envelopes distort to increase contact area with the positively charged platelet edges indicating that the virion surface is negatively charged. The nucleocapsid (NCs) remaining after envelope removal also exhibit distortion, in contrast to detergent-produced NCs which exhibit no distortion. This visually discernible disassembly is a mechanism for loss of infectivity previously unreported by studies of nonenveloped viruses. The MMT-mediated sequestration and disassembly result in reduced infectivity, suggesting that clays may reduce infectivity of enveloped pathogenic viruses in soils and sediments. PMID:24357622

  10. Physiochemical Changes and Optimization of Phosphate-Treated Shrimp (Litopenaeus vannamei ) Using Response Surface Methodology

    PubMed Central

    Omar, Saiah Djebbour; Yang, Je-Eun; Oh, Sang-Cheol; Kim, Dae-Wook; Lee, Yang-Bong

    2016-01-01

    The objective of this study was to determine the factors responsible for the changed physiochemical properties of unpeeled shrimp treated in cold phosphate solution (2~4°C) with the intervention of 4 factors: phosphate concentration, dipping time, rotation speed, and volume of brine solution. Response surface analysis was used to characterize the effect of the phosphate treatment on shrimps by running 33 treatments for optimizing the experiment. For each treatment, phosphate amount, moisture content, and weight gain were measured. The results showed that phosphate concentration is the most important factor than other factors for facilitating phosphate penetration in the meat of the shrimp and for getting the best result. The optimum condition of phosphate-treated shrimp in this study was 110 to 120 min dipping time, 500 to 550 mL brine solution for 100 g shrimp sample, and 190 to 210 rpm agitation speed. The studied conditions can be applied in fisheries and other food industries for good phosphate treatments. PMID:27069905

  11. Optimization of electrocoagulation process to treat grey wastewater in batch mode using response surface methodology

    PubMed Central

    2014-01-01

    Background Discharge of grey wastewater into the ecological system causes the negative impact effect on receiving water bodies. Methods In this present study, electrocoagulation process (EC) was investigated to treat grey wastewater under different operating conditions such as initial pH (4–8), current density (10–30 mA/cm2), electrode distance (4–6 cm) and electrolysis time (5–25 min) by using stainless steel (SS) anode in batch mode. Four factors with five levels Box-Behnken response surface design (BBD) was employed to optimize and investigate the effect of process variables on the responses such as total solids (TS), chemical oxygen demand (COD) and fecal coliform (FC) removal. Results The process variables showed significant effect on the electrocoagulation treatment process. The results were analyzed by Pareto analysis of variance (ANOVA) and second order polynomial models were developed in order to study the electrocoagulation process statistically. The optimal operating conditions were found to be: initial pH of 7, current density of 20 mA/cm2, electrode distance of 5 cm and electrolysis time of 20 min. Conclusion These results indicated that EC process can be scale up in large scale level to treat grey wastewater with high removal efficiency of TS, COD and FC. PMID:24410752

  12. Physiochemical Changes and Optimization of Phosphate-Treated Shrimp (Litopenaeus vannamei ) Using Response Surface Methodology.

    PubMed

    Omar, Saiah Djebbour; Yang, Je-Eun; Oh, Sang-Cheol; Kim, Dae-Wook; Lee, Yang-Bong

    2016-03-01

    The objective of this study was to determine the factors responsible for the changed physiochemical properties of unpeeled shrimp treated in cold phosphate solution (2~4°C) with the intervention of 4 factors: phosphate concentration, dipping time, rotation speed, and volume of brine solution. Response surface analysis was used to characterize the effect of the phosphate treatment on shrimps by running 33 treatments for optimizing the experiment. For each treatment, phosphate amount, moisture content, and weight gain were measured. The results showed that phosphate concentration is the most important factor than other factors for facilitating phosphate penetration in the meat of the shrimp and for getting the best result. The optimum condition of phosphate-treated shrimp in this study was 110 to 120 min dipping time, 500 to 550 mL brine solution for 100 g shrimp sample, and 190 to 210 rpm agitation speed. The studied conditions can be applied in fisheries and other food industries for good phosphate treatments. PMID:27069905

  13. Influence of montmorillonite on antimicrobial activity of tetracycline and ciprofloxacin

    NASA Astrophysics Data System (ADS)

    Lv, Guocheng; Pearce, Cody W.; Gleason, Andrea; Liao, Libing; MacWilliams, Maria P.; Li, Zhaohui

    2013-11-01

    Antibiotics are used not only to fight infections and inhibit bacterial growth, but also as growth promotants in farm livestock. Farm runoff and other farm-linked waste have led to increased antibiotic levels present in the environment, the impact of which is not completely understood. Soil, more specifically clays, that the antibiotic contacts may alter its effectiveness against bacteria. In this study a swelling clay mineral montmorillonite was preloaded with antibiotics tetracycline and ciprofloxacin at varying concentrations and bioassays were conducted to examine whether the antibiotics still inhibited bacterial growth in the presence of montmorillonite. Escherichia coli was incubated with montmorillonite or antibiotic-adsorbed montmorillonite, and then the number of viable bacteria per mL was determined. The antimicrobial activity of tetracycline was affected in the presence of montmorillonite, as the growth of non-resistant bacteria was still found even when extremely high TC doses were used. Conversely, in the presence of montmorillonite, ciprofloxacin did inhibit E. coli bacterial growth at high concentrations. These results suggest that the effectiveness of antimicrobial agents in clayey soils depends on the amount of antibiotic substance present, and on the interactions between the antibiotic and the clays in the soil, as well.

  14. Biocompatibility evaluation of surface-treated AISI 316L austenitic stainless steel in human cell cultures.

    PubMed

    Martinesi, M; Bruni, S; Stio, M; Treves, C; Bacci, T; Borgioli, F

    2007-01-01

    The effects of AISI 316L austenitic stainless steel, tested in untreated state or subjected to glow-discharge nitriding (at 10 or 20 hPa) and nitriding + post-oxidizing treatments, on human umbilical vein endothelial cells (HUVEC) and on peripheral blood mononuclear cells (PBMC) were evaluated. All the treated samples showed a better corrosion resistance in PBS and higher surface hardness in comparison with the untreated alloy. In HUVEC put in contact for 72 h with the sample types, proliferation and apoptosis decreased and increased, respectively, in the presence of the nitrided + post-oxidized samples, while only slight differences in cytokine (TNF-alpha, IL-6, and TGF-beta1) release were registered. Intercellular adhesion molecule-1 (ICAM-1) increased in HUVEC incubated with all the treated samples, while vascular cell adhesion molecule-1 (VCAM-1) and E-selectin increased in the presence of all the sample types. PBMC incubated for 48 h with the samples showed a decrease in proliferation and an increase in apoptosis in the presence of the untreated samples and the nitrided + post-oxidized ones. All the sample types induced a remarkable increase in TNF-alpha and IL-6 release in PBMC culture medium, while only the untreated sample and the nitrided at 10 hPa induced an increase in ICAM-1 expression. In HUVEC cocultured with PBMC, previously put in contact with the treated AISI 316L samples, increased levels of ICAM-1 were detected. In HUVEC coincubated with the culture medium of PBMC, previously put in contact with the samples under study, a noteworthy increase in ICAM-1, VCAM-1, and E-selectin levels was always registered, with the exception of VCAM-1, which was not affected by the untreated sample. In conclusion, even if the treated samples do not show a marked increase in biocompatibility in comparison with the untreated alloy, their higher corrosion resistance may suggest a better performance as the contact with physiological environment becomes longer. PMID

  15. LiBr treated porous silicon used for efficient surface passivation of crystalline silicon solar cells

    NASA Astrophysics Data System (ADS)

    Zarroug, Ahmed; Haddadi, Ikbel; Derbali, Lotfi; Ezzaouia, Hatem

    2015-04-01

    A simple but effective passivation method of both front and rear surfaces using porous silicon (PS) has been developed. This paper investigates the effect of LiBr on the passivation of PS. The immersion of as-etched PS in dilute LiBr solution followed by an annealing in an infrared furnace, under a controlled atmosphere at different temperatures, led to the passivation of the PS layer and the improvement of the electronic properties of the crystalline silicon substrates. The influence of substrate temperature was investigated, since the processed wafers were found to be sensitive to heat, which in turn was optimized to have a gettering effect. The bromide of lithium can effectively saturate dangling bonds and hence contributed to the formation of a stable passivation film, at both front and back surfaces. Such a reaction was found to have a beneficial effect on the passivation process of the PS layer grown on both sides. The obtained results exhibited a significant improvement of the minority carrier lifetime, which is an important parameter that defines the quality of crystalline silicon substrates, and an apparent enhancement of its photoluminescence (PL). The internal quantum efficiency was investigated and found to be significantly improved. The qualitative effect of the above-mentioned procedure proved a significant enhancement of the electronic quality of the treated substrates.

  16. [Joint prostheses components of warm-forged and surface treated Ti-6Al-7Nb alloy].

    PubMed

    Semlitsch, M; Weber, H; Streicher, R M; Schön, R

    1991-05-01

    In 1978 development of a TiAl alloy with the inert alloying element niobium was initiated. In 1984, the optimal composition was found to be Ti-6Al-7Nb (Protasul-100). This custom-made alloy for implants has the same alpha/beta micro-structure and equally good mechanical properties as Ti-6Al-4V. The corrosion resistance of Ti-6Al-7Nb is better than that of pure titanium and Ti-6Al-4V, due to the very dense and stable passive layer. Since 1985, highly stressed anchoring stems of various hip prosthesis designs have been manufactured from hot-forged Ti-6Al-7Nb/Protasul-100. Polished surfaces of hip, knee or wrist joints made of Ti-6Al-7Nb intended to articulate with polyethylene are surface-treated by the application of a very hard, 3-5 microns thick titanium nitride coating (Tribosul-TiN), or by oxygen diffusion hardening (Tribosul-ODH) to a depth of 30 microns. PMID:1859861

  17. Wastewater effects on montmorillonite suspensions and hydraulic properties of sandy soils

    SciTech Connect

    Tarchitzky, J.; Golobati, Y.; Keren, R.; Chen, Y.

    1999-06-01

    Recycled wastewater effluent is an important source of irrigation water in arid and semiarid regions. In these regions, however, irrigation water quality is one of the main factors limiting plant growth. Wastewater effluents generally contain high concentrations of suspended and dissolved solids, both organic and inorganic. Inorganic dissolved solids are only minimally removed from the effluent during conventional sewage treatment. As a result, most of the salts added during domestic and industrial usage remain in the irrigation water and may eventually reach the soil. A number of researchers have reported reduced hydraulic conductivity for soils to which treated wastewater has been applied. In this research, the influence of dissolved organic matter (DOM) contained in reclaimed wastewater effluents on the flocculation of montmorillonite and on the hydraulic properties of soils was studied. Flocculation values (FVs) for Na-montmorillonite increased with increasing concentrations of DOM at all pH levels analyzed. Maximum FV levels were exhibited for Na-montmorillonite at the highest DOM concentrations. The effect of DOM on FV can be explained by the mechanisms of edge-charge reversal and mutual flocculation. The hydraulic conductivity (HC) of a sandy soil was determined in the laboratory by leaching columns with an electrolyte solution chemically similar to that of the wastewater effluent (but without DOM). In columns treated with wastewater effluent, the HC exhibited a sharp decrease to only 20% of its initial value. The adverse effect of DOM on HC was evident for this soil despite a relatively low exchangeable sodium percentage (ESP). The reduction in HC is likely to be the result of decreases soil pore-size, which reflects two processes: (1) retention of part of the DOM during water percolation; and (2) a change in pore-size distribution due to swelling and dispersion of clay particles. The latter may result from a higher percentage of adsorbed sodium combined

  18. Preparation of ZrO2/Al2O3-montmorillonite composite as catalyst for phenol hydroxylation

    PubMed Central

    Fatimah, Is

    2013-01-01

    Zirconium dispersed in aluminum-pillared montmorillonite was prepared as a catalyst for phenol hydroxylation. The effects of varying the Zr content on the catalyst’s physicochemical character and activity were studied with XRD, BET surface area analysis, surface acidity measurements and scanning electron microscopy before investigating the performance for phenol conversion. The zirconia dispersion significantly affects the specific surface area, the total surface acidity and surface acidity distribution related to the formation of porous zirconia particles on the surface. The prepared samples exhibited excellent catalytic activity during phenol hydroxylation. PMID:25685535

  19. The Effect of Surface Treated Nanoparticles on Single and Multi-Phase Flow in Porous Media

    NASA Astrophysics Data System (ADS)

    DiCarlo, D. A.; Aminzadeh, B.; Chung, D.; Zhang, X.; Wung, R.; Huh, C.; Bryant, S. L.

    2013-12-01

    Surface treated nanoparticles have been suggested to be an additive to CO2 storage scenarios. This is because 1) the nanoparticles have been shown to freely transport through permeable media, and 2) the nanoparticles can stabilize a CO2 in water foam by adhering to the surface of CO2 bubbles/droplets preventing their coalescence. In terms of storage, The formation of CO2 foam will limit the CO2 mobility which can potentially help limit the CO2 leakage. Here, we will show how nanoparticles in porous media can have many interesting properties in single and multi-phase flow. For multi-phase CO2, we have performed experiments where high pressure liquid CO2 displaces brine and vice versa with and without nanoparticles in the brine. We measure the displacement pattern and in-situ CO2 saturation using CT scanning and measure the pressure drop using pressure transducers. We find that the flow is less preferential and the pressure drop is greater than when nanoparticles are present. This suggest the formation of in-situ foam/emulsion. We also show that on a brine chase, the residual saturation of CO2 is greater in the presence of nanoparticles. In terms of nanoparticle transport, it is observed that nanoparticles accumulate at the front of a brine/octane displacement. We hypothesize that this occurs due to the nanoparticles being size excluded from portions of the pore-space. To determine if this occurs in single phase flow, we have also performed experiments single-phase flow with the nanoparticles and tracer. We find that the nanoparticles arrive roughly 5% faster than the tracer. This also has implications for the positioning of nanoparticles in the pore space and how this can change the effective viscosity of the nanoparticle suspension.

  20. Properties of thermo-chemically surface treated carbon fibers and of their epoxy and vinyl ester composites

    SciTech Connect

    Vautard, Frederic; Ozcan, Soydan; Meyer III, Harry M

    2012-01-01

    High strength carbon fibers were surface treated by a continuous gas phase thermo-chemical surface treatment. The surface and the mechanical properties of the fibers were investigated before and after treatment and compared to the properties obtained with a conventional industrial electro-chemical surface treatment. An increase of the oxygen atomic content from 3 % to 20 % with a preferential generation of carboxylic acid functionalities and hydroxyl groups was highlighted after the thermo-chemical surface treatment, compared to an oxygen atomic content of 7 % and a wide variety of oxygen moieties with the electro-chemical surface treatment. The tensile strength of the fibers increased slightly after the thermo-chemical surface treatment and remained the same after the electro-chemical surface treatment. Short beam shear and 90 flexural tests of composites revealed that the improvement of interfacial adhesion with a vinyl ester matrix was limited, revealing that oxidation of the carbon fiber surface alone cannot tremendously improve the mechanical properties of carbon fiber-vinyl ester composites. Atomic force microscopy showed that the creation of roughness with both surface treatments at a nanometric scale. Although the surface is slightly rougher after the electro-chemical surface treatment and is expected to lead to higher adhesion due to mechanical interlocking between the fiber surface and the matrix, the effect of covalent bonding coming from the high concentration of chemical groups on the surface results in higher adhesion strength, as obtained with the thermo-chemical surface treatment.

  1. Effects of exchanged cation on the microporosity of montmorillonite

    USGS Publications Warehouse

    Rutherford, D.W.; Chiou, C.T.; Eberl, D.D.

    1997-01-01

    The micropore volumes of 2 montmorillonites (SAz- 1 and SWy-1), each exchanged with Ca, Na, K, Cs and tetramethylammonium (TMA) ions, were calculated from the measured vapor adsorption data of N2 and neo-hexane by use of t- and ??s-plots. The corresponding surface areas of the exchanged clays were determined from Brunauer-Emmett-Teller (BET) plots of N2 adsorption data. Micropore volumes and surface areas of the samples increased with the size of exchanged cation: TMA > Cs > K> Ca > Na. The SAz-1 exchanged clays showed generally greater micropore volumes and surface areas than the corresponding SWy-1 clays. The vapor adsorption data and d(001) measurements for dry clay samples were used together to evaluate the likely locations and accessibility of clay micropores, especially the relative accessibility of their interlayer spacing. For both source clays exchanged with Na, Ca and K ions, the interlayer spacing appeared to be too small to admit nonpolar gases and the accessible micropores appeared to have dimensions greater than 5.0 A??, the limiting molecular dimension of neo -hexane. In these systems, there was a good consistency of micropore volumes detected by N2 and neo-hexane. When the clays were intercalated with relatively large cations (TMA and possibly Cs), the large layer expansion created additional microporosity, which was more readily accessible to small N2 than to relatively large neo-hexane. Hence, the micropore volume as detected by N2 was greater than that detected by neo-hexane. The micropore volumes with pore dimensions greater than 5 A?? determined for clays exchanged with Na, Ca and K likely resulted from the pores on particle edges and void created by overlap regions of layers. The increase in micropore volumes with pore dimensions less than 5 A?? determined for clays exchanged with TMA and possibly Cs could be caused by opening of the interlayer region by the intercalation of these large cations.

  2. Surface chemical changes of atmospheric pressure plasma treated rabbit fibres important for felting process

    NASA Astrophysics Data System (ADS)

    Štěpánová, Vlasta; Slavíček, Pavel; Stupavská, Monika; Jurmanová, Jana; Černák, Mirko

    2015-11-01

    We introduce the atmospheric pressure plasma treatment as a suitable procedure for in-line industrial application of rabbit fibres pre-treatment. Changes of rabbit fibre properties due to the plasma treatment were studied in order to develop new technology of plasma-based treatment before felting. Diffuse Coplanar Surface Barrier Discharge (DCSBD) in ambient air at atmospheric pressure was used for plasma treatment. Scanning electron microscopy was used for determination of the fibres morphology before and after plasma treatment. X-ray photoelectron spectroscopy and attenuated total reflectance-Fourier transform infrared spectroscopy were used for evaluation of reactive groups. The concentration of carbon decreased and conversely the concentration of nitrogen and oxygen increased after plasma treatment. Aging effect of plasma treated fibres was also investigated. Using Washburn method the significant increase of fibres wettability was observed after plasma treatment. New approach of pre-treatment of fibres before felting using plasma was developed. Plasma treatment of fibres at atmospheric pressure can replace the chemical method which consists of application of strong acids on fibres.

  3. Fungistatic activity of heat-treated flaxseed determined by response surface methodology.

    PubMed

    Xu, Y; Hall, C; Wolf-Hall, C

    2008-08-01

    The objective of this study was to evaluate the effect of heat treatment on the fungistatic activity of flaxseed (Linum usitatissimum) in potato dextrose agar (PDA) medium and a fresh noodle system. The radial growth of Penicilliumn chrysogenum, Aspergillus flavus, and a Penicillium sp. isolated from moldy noodles, as well as the mold count of fresh noodle enriched with heat treated flaxseed, were used to assess antifungal activity. A central composite design in the response surface methodology was used to predict the effect of heating temperature and time on antifungal activity of flaxseed flour (FF). Statistical analysis determined that the linear terms of both variables (that is, heating temperature and time) and the quadratic terms of the heating temperature had significant (P<0.05) effects on the radial growth of all 3 test fungi and the mold count log-cycle reduction of fresh noodle. The interactions between the temperature and time were significant for all dependent variables (P<0.05). Significant reductions in antifungal activities were found when FF was subjected to high temperatures, regardless of heating time. In contrast, prolonging the heating time did not substantially affect the antifungal activities of FF at low temperature. However, 60% of the antifungal activity was retained after FF was heated at 100 degrees C for 15 min, which suggests a potential use of FF as an antifungal additive in food products subjected to low to mild heat treatments. PMID:19241553

  4. Purification ability and carbon dioxide flux from surface flow constructed wetlands treating sewage treatment plant effluent.

    PubMed

    Wu, Haiming; Lin, Li; Zhang, Jian; Guo, Wenshan; Liang, Shuang; Liu, Hai

    2016-11-01

    In this study, a two-year experiment was carried out to investigate variation of carbon dioxide (CO2) flux from free water surface constructed wetlands (FWS CW) systems treating sewage treatment plant effluent, and treatment performance was also evaluated. The better 74.6-76.6% COD, 92.7-94.4% NH4(+)-N, 60.1-84.7% TN and 49.3-70.7% TP removal efficiencies were achieved in planted CW systems compared with unplanted systems. The planted CW was a net CO2 sink, while the unplanted CW was a net CO2 source in the entire study period. An obvious annual and seasonal variability of CO2 fluxes from different wetland systems was also presented with the average CO2 flux ranging from -592.83mgm(-2)h(-1) to 553.91mgm(-2)h(-1) during 2012-2013. In addition, the net exchange of CO2 between CW systems and the atmosphere was significantly affected by air temperature, and the presence of plants also had the significant effect on total CO2 emissions. PMID:27544264

  5. The origin of the pozzolanic activity of calcined clay minerals: A comparison between kaolinite, illite and montmorillonite

    SciTech Connect

    Fernandez, Rodrigo; Martirena, Fernando; Scrivener, Karen L.

    2011-01-15

    This paper investigates the decomposition of three clayey structures (kaolinite, illite and montmorillonite) when thermally treated at 600 {sup o}C and 800 {sup o}C and the effect of this treatment on their pozzolanic activity in cementitious materials. Raw and calcined clay minerals were characterized by the XRF, XRD, {sup 27}Al NMR, DTG and BET techniques. Cement pastes and mortars were produced with a 30% substitution by calcined clay minerals. The pozzolanic activity and the degree of hydration of the clinker component were monitored on pastes using DTG and BSE-IA, respectively. Compressive strength and sorptivity properties were assessed on standard mortars. It was shown that kaolinite, due to the amount and location of OH groups in its structure, has a different decomposition process than illite or montmorillonite, which results in an important loss of crystallinity. This explains its enhanced pozzolanic activity compared to other calcined clay-cement blends.

  6. Measuring the isoelectric point of the edges of clay mineral particles: the case of montmorillonite.

    PubMed

    Pecini, Eliana M; Avena, Marcelo J

    2013-12-01

    The isoelectric point (IEP) of the edge surface of a montmorillonite sample was determined by using electrophoretic mobility measurements. This parameter, which is fundamental for the understanding of the charging behavior of clay mineral surfaces, was never measured so far because of the presence of permanent negative charges within the montmorillonite structure, charges that mask the electrokinetic behavior of the edges. The strategy was to block or neutralize the structural charges with two different cations, methylene blue (MB(+)) and tetraethylenepentaminecopper(II) ([Cu(tetren)](2+)), so that the charging behavior of the particles becomes that of the edge surfaces. Adsorption isotherms of MB(+) and [Cu(tetren)](2+) at different ionic strengths (NaCl) were performed to establish the uptakes that neutralize the cation exchange capacity (CEC, 0.96 meq g(-1)) of the sample. At high adsorptive concentrations, there was a superequivalent adsorption of MB(+) (adsorption exceeding the CEC) and an equivalent adsorption of [Cu(tetren)](2+) (adsorption reaching the CEC). In both cases, structural charges were neutralized at uptakes very close to the CEC. Zeta potential (ζ) vs pH data at different ionic strengths of montmorillonite with adsorbed MB(+) allowed to estimate an upper limit of the edge's IEP, 5.3 ± 0.2. The same kind of data obtained with adsorbed [Cu(tetren)](2+) provided a lower limit of the IEP, 4.0 ± 0.2. These values are in agreement with previously informed IEP and point of zero charge of pyrophyllite, which is structurally analogous to montmorillonite but carries no permanent charges. The importance of knowing the IEP of the edge surface of clay minerals is discussed. This value characterizes the intrinsic reactivity of edges, that is, the protonating capacity of edge groups in absence of any electric field generated by structural charges. It also allows us to correct relative edge charge vs pH curves obtained by potentiometric titrations and to

  7. Surface chemistry and optical property of TiO{sub 2} thin films treated by low-pressure plasma

    SciTech Connect

    Dhayal, Marshal Jun, Jin; Gu, Hal Bon; Hee Park, Kyung

    2007-10-15

    The low temperature RF plasma treatment was used to control the surface chemistry and optical property of TiO{sub 2} thin films deposited by RF magnetron sputtering with a very good uniformity at 300 deg. C substrate heating temperature. The XRD pattern indicates the crystalline structure of the film could be associated to amorphous structure of TiO{sub 2} in thin film. The plasma treatment of TiO{sub 2} film can increase the proportion of Ti{sup 3+} in Ti2p and decrease in carbon atoms as alcohol/ether group in C1s at the surface. The optical transmittance of the film was enhanced by 50% after the plasma treatment. The surface structure and morphology remain the same for untreated and low-pressure plasma-treated films. Therefore, increase in the optical transmission could be due to change in surface chemistry and surface cleaning by plasma treatment. - Graphical abstract: The surface chemistry and surface states of TiO{sub 2} films was modified using low-pressure RF plasma treatment. The surface roughness and crystalline structure remain unchanged for low-pressure plasma-treated films. There was an increase in the Ti{sup 3+} surface states of Ti2p at the surface and this can be useful to increase the photocatalytic activities of TiO{sub 2} films. The proportion of carbon atoms as carboxyl group in C1s was also increased after plasma treatment. All the plasma-treated films show a higher optical transmittance when untreated and it was increased when the power was increased. The increase in the optical transmission could be due to surface cleaning of films by plasma treatment and possibly due to change in the surface chemistry.

  8. Efficient Removal of Co2+ from Aqueous Solution by 3-Aminopropyltriethoxysilane Functionalized Montmorillonite with Enhanced Adsorption Capacity.

    PubMed

    Huang, Zhujian; Wu, Pingxiao; Gong, Beini; Dai, Yaping; Chiang, Pen-Chi; Lai, Xiaolin; Yu, Guangwei

    2016-01-01

    To achieve a satisfactory removal efficiency of heavy metal ions from wastewater, silane-functionalized montmorillonite with abundant ligand-binding sites (-NH2) was synthesized as an efficient adsorbent. Ca-montmorillonite (Ca-Mt) was functionalized with 3-aminopropyl triethoxysilane (APTES) to obtain the APTES-Mt products (APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt, APTES4.0CEC-Mt) with enhanced adsorption capacity for Co2+. The physico-chemical properties of the synthesized adsorbents were characterized by spectroscopic and microscopic methods, and the results demonstrated that APTES was successfully intercalated into the gallery of Ca-Mt or grafted onto the surface of Ca-Mt through Si-O bonds. The effect of solution pH, ionic strength, temperature, initial concentrations and contact time on adsorption of Co2+ by APTES-Mt was evaluated. The results indicated that adsorption of Co2+ onto Ca-Mt, APTES1.0CEC-Mt and APTES2.0CEC-Mt can be considered to be a pseudo-second-order process. In contrast, adsorption of Co2+ onto APTES3.0CEC-Mt and APTES4.0CEC-Mt fitted well with the pseudo-first-order kinetics. The adsorption isotherms were described by the Langmuir model, and the maximum adsorption capacities of APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt and APTES4.0CEC-Mt were 25.1, 33.8, 61.6, and 61.9 mg·g-1, respectively. In addition, reaction temperature had no impact on the adsorption capacity, while both the pH and ionic strength significantly affected the adsorption process. A synergistic effect of ion exchange and coordination interactions on adsorption was observed, thereby leading to a significant enhancement of Co2+ adsorption by the composites. Thus, APTES-Mt could be a cost-effective and environmental-friendly adsorbent, with potential for treating Co2+-rich wastewater. PMID:27448094

  9. Efficient Removal of Co2+ from Aqueous Solution by 3-Aminopropyltriethoxysilane Functionalized Montmorillonite with Enhanced Adsorption Capacity

    PubMed Central

    Huang, Zhujian; Gong, Beini; Dai, Yaping; Chiang, Pen-Chi; Lai, Xiaolin; Yu, Guangwei

    2016-01-01

    To achieve a satisfactory removal efficiency of heavy metal ions from wastewater, silane-functionalized montmorillonite with abundant ligand-binding sites (-NH2) was synthesized as an efficient adsorbent. Ca-montmorillonite (Ca-Mt) was functionalized with 3-aminopropyl triethoxysilane (APTES) to obtain the APTES-Mt products (APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt, APTES4.0CEC-Mt) with enhanced adsorption capacity for Co2+. The physico-chemical properties of the synthesized adsorbents were characterized by spectroscopic and microscopic methods, and the results demonstrated that APTES was successfully intercalated into the gallery of Ca-Mt or grafted onto the surface of Ca-Mt through Si-O bonds. The effect of solution pH, ionic strength, temperature, initial concentrations and contact time on adsorption of Co2+ by APTES-Mt was evaluated. The results indicated that adsorption of Co2+ onto Ca-Mt, APTES1.0CEC-Mt and APTES2.0CEC-Mt can be considered to be a pseudo-second-order process. In contrast, adsorption of Co2+ onto APTES3.0CEC-Mt and APTES4.0CEC-Mt fitted well with the pseudo-first-order kinetics. The adsorption isotherms were described by the Langmuir model, and the maximum adsorption capacities of APTES1.0CEC-Mt, APTES2.0CEC-Mt, APTES3.0CEC-Mt and APTES4.0CEC-Mt were 25.1, 33.8, 61.6, and 61.9 mg·g-1, respectively. In addition, reaction temperature had no impact on the adsorption capacity, while both the pH and ionic strength significantly affected the adsorption process. A synergistic effect of ion exchange and coordination interactions on adsorption was observed, thereby leading to a significant enhancement of Co2+ adsorption by the composites. Thus, APTES-Mt could be a cost-effective and environmental-friendly adsorbent, with potential for treating Co2+-rich wastewater. PMID:27448094

  10. Polymerization of alanine in the presence of a non-swelling montmorillonite

    NASA Technical Reports Server (NTRS)

    Paecht-Horowitz, M.; Lahav, N.

    1977-01-01

    Alanine, starting from alanine-adenylate, has been polymerized in the presence of non-swelling Al-montmorillonite. The yield of polymerization is much lower than that obtained in the presence of swelling Na-montmorillonite. The possibility that the changing interlayer spacing in Na-montmorillonite might be responsible for its catalytic properties, is discussed.

  11. Commenting on the effects of surface treated- and non-surface treated TiO2 in the Caco-2 cell model

    PubMed Central

    2012-01-01

    In a recent work published in Particle and Fibre Toxicology by Fisichella and coworkers investigating surface-modified TiO2 nanoparticle exposure in a model human intestinal epithelium (Caco-2), albeit degraded to mimic conditions in the gut and exposure to natural sunlight, purportedly resulted in no toxic effects. The authors (Fisichella et al.) claim to have confirmed the results of a 2010 report by Koeneman et al. However, the study by Koeneman and colleagues revealed significant effects of unmodified TiO2 nanoparticles. These contradicting data warrant further investigation into the possible effects of aluminum hydroxide, as these nanoparticles appear to have resulted in an abnormal apical surface in Caco-2 cells. This is a comment on http://www.particleandfibretoxicology.com/content/pdf/1743-8977-9-18.pdf. PMID:23146628

  12. The extraction of {sup 137}Cs and {sup 89}Sr from waste simulants using pillared montmorillonite

    SciTech Connect

    Sylvester, P.; Clearfield, A.

    1998-08-01

    Two samples of a silica-pillared montmorillonite produced using 3-aminopropyltrimethoxy silane and an alumina-pillared montmorillonite were evaluated for the removal of {sup 137}Cs and {sup 89}Sr from a simulated nuclear waste solution and a simulated groundwater, and the results were compared to the parent montmorillonite and two zeolites, AW500 (chabazite) and clinoptilolite. The parent and pillared clays were characterized using x-ray powder diffraction and surface area analysis by nitrogen adsorption/desorption studies. The pillared clays exhibited d-spacings of between 17.43 and 18.32 {angstrom} after calcination, and surface areas ranging from 71.3 to 264.4 m{sup 2}/g. Both of the silica-pillared clays and the alumina-pillared clay exhibited excellent K{sub d}s for {sup 137}Cs from simulated groundwater with values of 23,650, 23,260 and 144,570 mL/g, respectively. These were far better than the K{sub d}s obtained by clinoptilolite and AW500 which had K{sub d}s of only 14,560 and 9,650 mL/g, respectively. None of the pillared clays showed a high selectivity for {sup 89}Sr from groundwater or {sup 137}Cs from simulated alkaline tank waste. They did, however, show a slight selectivity for {sup 89}Sr in the simulated Hanford tank wastes, but this is thought to be due to a precipitation mechanism rather than to ion exchange.

  13. Comparison of alkaline phosphatase activity of MC3T3-E1 cells cultured on different Ti surfaces: modified sandblasted with large grit and acid-etched (MSLA), laser-treated, and laser and acid-treated Ti surfaces

    PubMed Central

    Li, Lin-Jie; Kim, So-Nam

    2016-01-01

    PURPOSE In this study, the aim of this study was to evaluate the effect of implant surface treatment on cell differentiation of osteoblast cells. For this purpose, three surfaces were compared: (1) a modified SLA (MSLA: sand-blasted with large grit, acid-etched, and immersed in 0.9% NaCl), (2) a laser treatment (LT: laser treatment) titanium surface and (3) a laser and acid-treated (LAT: laser treatment, acid-etched) titanium surface. MATERIALS AND METHODS The MSLA surfaces were considered as the control group, and LT and LAT surfaces as test groups. Alkaline phosphatase expression (ALP) was used to quantify osteoblastic differentiation of MC3T3-E1 cell. Surface roughness was evaluated by a contact profilometer (URFPAK-SV; Mitutoyo, Kawasaki, Japan) and characterized by two parameters: mean roughness (Ra) and maximum peak-to-valley height (Rt). RESULTS Scanning electron microscope revealed that MSLA (control group) surface was not as rough as LT, LAT surface (test groups). Alkaline phosphatase expression, the measure of osteoblastic differentiation, and total ALP expression by surface-adherent cells were found to be highest at 21 days for all three surfaces tested (P<.05). Furthermore, ALP expression levels of MSLA and LAT surfaces were significantly higher than expression levels of LT surface-adherent cells at 7, 14, and 21 days, respectively (P<.05). However, ALP expression levels between MSLA and LAT surface were equal at 7, 14, and 21 days (P>.05). CONCLUSION This study suggested that MSLA and LAT surfaces exhibited more favorable environment for osteoblast differentiation when compared with LT surface, the results that are important for implant surface modification studies. PMID:27350860

  14. Retention of gases by hexadecyltrimethylammonium-montmorillonite clays.

    PubMed

    Volzone, C; Rinaldi, J O; Ortiga, J

    2006-05-01

    Intercalated montmorillonite clays with different amounts of organic hexadecyltrimethylammonium (HDTMA) cations were studied to analyse their CO, CH(4), and SO(2) gas retentions. Equilibrium adsorption was measured by using a standard volumetric apparatus at 25 degrees C and 0.1 MPa. The solids were characterised by X-ray diffraction. The levels of adsorption of SO(2) by organo-montmorillonites (0.3595-1.6403 mmol/g) were higher than those of CO (up to 0.0202 mmol/g) and CH(4) (up to 0.0273 mmol/g) gases. HDTMA montmorillonites may be effective adsorbents for removing SO(2) and for its potential separation in the presence of CO and/or CH(4) molecules, which can be present in contaminated air. PMID:16182436

  15. Speciation of uranium(VI) sorption complexes on montmorillonite

    SciTech Connect

    Chisholm-Brause, C.J.; Morris, D.E.; Richard, R.E.

    1992-05-01

    Environmental contaminant releases that contain uranium are among the most serious problems that must be confronted by restoration programs. To facilitate restoration, information concerning the speciation of uranium is needed. Under oxidizing conditions, dissolved uranium is predominantly in the U(VI) (uranyl) form and is quite mobile in the environment, however sorption onto soils may retard its movement. In this study, we have investigated the effects of changes in solution speciation on the nature of uranyl sorption complexes on montmorillonite, a common soil constituent. Aqueous U(VI) solutions between pH 3 to 7 were batch-equilibrated with montmorillonite for several days; specific pH values were selected such that the solutions consisted of dominantly monomeric, oligomeric, or a mix of monomeric and oligomeric aqueous uranyl species. Emission spectroscopy was used to investigate the nature of U(VI) sorbed to montmorillonite.

  16. Formation of RNA oligomers on montmorillonite: site of catalysis

    NASA Technical Reports Server (NTRS)

    Ertem, G.; Ferris, J. P.

    1998-01-01

    Certain montmorillonites catalyze the self condensation of the 5'-phosphorimidazolide of nucleosides in pH 8 aqueous electrolyte solutions at ambient temperatures leading to formation of RNA oligomers. In order to establish the nature of the sites on montmorillonite responsible for this catalytic activity, oligomerization reactions were run with montmorillonites which had been selectively modified (I) at the edges by (a) fluoride treatment, (b) silylation, (c) metaphosphate treatment of the anion exchange sites (II) in the interlayer by (a) saturation with quaternary alkylammonium ions of increasing size, (b) aluminum polyoxo cations. High pressure liquid chromatography, HPLC, analysis of condensation products for their chain lengths and yields indicated that modification at the edges did not affect the catalytic activity to a significant extent, while blocking the interlayer strongly inhibited product formation.

  17. Hybrid collagen-based hydrogels with embedded montmorillonite nanoparticles.

    PubMed

    Nistor, Manuela Tatiana; Vasile, Cornelia; Chiriac, Aurica P

    2015-08-01

    Montmorillonite nanoparticles have been physically incorporated within a crosslinked collagen/poly(N-isopropyl acrylamide) network in order to adjust the properties of the stimuli-responsive hybrid systems. The research underlines both the influence of hydrogel composition and nanoparticle type on hybrid hydrogel properties. The dispersion of the montmorillonite nanoparticles in polymeric matrix have been visualized by SEM, TEM and AFM techniques and quantitatively and qualitatively estimated using near infrared chemical imaging. The electrical charge of the nanoparticles influenced the polymeric chain arrangement and the pore size. The morphologies of the nanoparticulated layers are partially exfoliated or intercalated and uniformly dispersed through the polymeric semi-interpenetrated network based on collagen and poly(N-isopropyl acrylamide). The hybrid hydrogels exhibit pseudoplastic behavior and the addition of nanoparticles has resulted in the increase of the complex viscosity. The adhesion capacity was affected mainly by the presence of organically modified montmorillonites. PMID:26042709

  18. Immobilization of self-assembled pre-dispersed nano-TiO2 onto montmorillonite and its photocatalytic activity.

    PubMed

    Zhang, Tingting; Luo, Yuan; Jia, Bing; Li, Yan; Yuan, Lingling; Yu, Jiang

    2015-06-01

    The immobilization of pre-dispersed TiO2 colloids onto the external surface of the clay mineral montmorillonite (Mt) was accomplished and regulated via a self-assembly method employing the cationic surfactant cetyltrimethylammonium bromide (CTAB). The role of CTAB in the synthesis process was investigated by preparing a series of TiO2-CTAB-Mt composites (TCM) with various CTAB doses. The results indicated that a uniform and continuous TiO2 film was deposited on the external surface of montmorillonite in the composite synthesized with 0.1 wt.% of CTAB, and the TCM nano-composites showed much higher values for specific surface area, average pore size and pore volume than the raw montmorillonite clay. Then, the formed TCM materials were applied in photocatalytic degradation of 2,4-dichlorophenol (2,4-DCP) in aqueous solution. The degradation efficiency reached as high as 94.7%. Based on the degradation intermediates benezoquinone, fumaric acid and oxalic acid identified by LC-MS analysis, a mechanism for the photocatalytic oxidation of 2,4-DCP on TiO2/Mt nano-composites is proposed. PMID:26040737

  19. Arsenate adsorption and desorption kinetics on a Fe(III)-modified montmorillonite.

    PubMed

    Luengo, Carina; Puccia, Virginia; Avena, Marcelo

    2011-02-28

    The adsorption-desorption kinetics of arsenate on a Fe(III)-modified montmorillonite (Fe-M) was studied at different arsenate concentrations, pH and stirring rates. The synthesized solid was a porous sample with Fe(III) present as a mix of monomeric and polymeric Fe(III) species in the interlayer and on the external surface. Adsorption took place in a two-step mechanism, with an initial fast binding of arsenate to Fe(III) species at the external surface (half-lives of 1 min or shorter) followed by a slower binding to less accessible Fe(III) species in pores and the interlayer (half-lives of around 1 h). Desorption kinetics also reflected the presence of externally and internally adsorbed arsenate. At pH 6 the maximum adsorbed arsenate was 52 μmol/g, a value that is low as compared to adsorption on ferrihydrite (700 μmol/g) and goethite (192-220 μmol/g). However, since the Fe(III) content of Fe-M is much lower than that of ferrihydrite and goethite, Fe(III) species in Fe-M are more efficient in binding arsenate than in ferrihydrite or goethite (one As atom is attached every 8.95 iron atoms). This high binding efficiency indicates that Fe(III) species are well spread on montmorillonite, forming small oligomeric species or surface clusters containing just a few iron atoms. PMID:21242027

  20. Five year water and nitrogen balance for a constructed surface flow wetland treating agricultural drainage waters.

    PubMed

    Borin, Maurizio; Tocchetto, Davide

    2007-07-15

    The performance of a constructed surface flow wetland in reducing diffuse N pollution coming from croplands is being investigated in an ongoing experiment, begun in 1998 in NE Italy. The 0.32 ha wetland is vegetated with Phragmites australis (Cav.) Trin. and Typha latifolia (L.). It receives drainage water from 6 ha of land managed for an experiment on drainage systems, where maize, sugarbeet, winter wheat and soybean are cultivated. During the period 1998-2002, the wetland received from 4698 to 8412 mm of water per year (on average, about 9 times the environmental rainfall); its water regimen was discontinuous and flooding occurred on a variable number of days per year (from 13 to 126). Nitric nitrogen was the most important form of element load. Its concentration in the inflow water over time was rather discontinuous, with median values ranging from 0.2 (in 2001) to 4.5 (in 2000) mg L(-1). Inflow nitric N concentrations were occasionally in the 5-15 mg L(-1) range. Concentrations reduced passing through the wetland, with a more evident effect in the last year. Over 5 years, the wetland received slightly more than 2000 kg ha(-1) of nitrogen, 87% in nitric form mostly from farmland drainage. The remaining 13% of N was applied as organic slurry directly onto the wetland, with 5 distributions during 1998 to assess wetland performance in treating occasional organic loads. Field drainage loads had a discontinuous time pattern and occurred mostly during autumn-winter, with the exception of the 2001-2002 season which was a very dry. The wetland discharged 206 kg ha(-1) of N, over the 5-year period, with an apparent removal efficiency of about 90%. The disappearance was mostly due to plant uptake (1110 kg ha(-1)) and soil accumulation (570 kg ha(-1)), with the contribution of denitrification being estimated at around 7%. PMID:17270250

  1. Effect of reactive species on surface crosslinking of plasma-treated polymers investigated by surface force microscopy

    SciTech Connect

    Tajima, S.; Komvopoulos, K.

    2006-09-18

    Polymer surface modification by ions, uncharged particles, and photons of inductively coupled Ar plasma was investigated with a surface force microscope. Optical windows consisting of crystals with different cutoff wavelengths and a metal shield were used to deconvolute the effects of the various plasma species on the modification of the surface nanomechanical properties of polyethylene. The extent of surface crosslinking was related to the frictional energy dissipated during nanoscratching. It is shown that surface crosslinking is primarily due to the simultaneous effects of uncharged particles and vacuum ultraviolet photons, while the ion bombardment effect is secondary.

  2. Modified montmorillonite as vector for gene delivery.

    PubMed

    Lin, Feng-Huei; Chen, Chia-Hao; Cheng, Winston T K; Kuo, Tzang-Fu

    2006-06-01

    Currently, gene delivery systems can be divided into two parts: viral or non-viral vectors. In general, viral vectors have a higher efficiency on gene delivery. However, they may sometimes provoke mutagenesis and carcinogenesis once re-activating in human body. Lots of non-viral vectors have been developed that tried to solve the problems happened on viral vectors. Unfortunately, most of non-viral vectors showed relatively lower transfection rate. The aim of this study is to develop a non-viral vector for gene delivery system. Montmorillonite (MMT) is one of clay minerals that consist of hydrated aluminum with Si-O tetrahedrons on the bottom of the layer and Al-O(OH)2 octahedrons on the top. The inter-layer space is about 12 A. The room is not enough to accommodate DNA for gene delivery. In the study, the cationic hexadecyltrimethylammonium (HDTMA) will be intercalated into the interlayer of MMT as a layer expander to expand the layer space for DNA accommodation. The optimal condition for the preparation of DNA-HDTMA-MMT is as follows: 1 mg of 1.5CEC HDTMA-MMT was prepared under pH value of 10.7 and with soaking time for 2 h. The DNA molecules can be protected from nuclease degradation, which can be proven by the electrophoresis analysis. DNA was successfully transfected into the nucleus of human dermal fibroblast and expressed enhanced green fluorescent protein (EGFP) gene with green fluorescence emission. The HDTMA-MMT has a great potential as a vector for gene delivery in the future. PMID:16488006

  3. Mechanisms of CO2 Interaction with Montmorillonite

    NASA Astrophysics Data System (ADS)

    Romanov, V.; Myshakin, E. M.; Howard, B.; Guthrie, G.

    2013-12-01

    Improved understanding of basic fluid-rock interactions can lead to more accurate models of the coupled fluid-flow and geomechanics in engineered geological systems. We studied carbon dioxide (CO2) interaction with source clay samples from The Clay Minerals Society. The manometric, infrared (IR) and X-ray diffraction (XRD) data indicated that montmorillonite can permanently trap CO2 molecules in its interlayer, after dynamic exposure to supercritical CO2. Such trapping is quite secure and appears to result in partial carbonate formation. Molecular dynamics simulations were carried out to investigate CO2 intercalation into the interlayer and its interaction with interlayer species. Previously reported results of simulations using simplified smectite models suggested that the experimentally observed red shift of the asymmetric-stretch vibrational mode for the trapped carbon dioxide can be attributed to induced polarization of the CO2 molecule by the interlayer water molecules. Modified smectite models were designed to account for the naturally occurring structural disorder that allows guest molecules to occupy localized interlamellar voids. In such models, energy dependences and structural rearrangements of the interlayer species are governed by rotational misalignment in turbostratically disordered clay. CO2 invasion in the interlayer disrupts the long-range ordering of water molecules and cations thus forcing the system to adopt energetically unfavorable configurations. New findings indicate that interaction between intercalated CO2 and H2O is limited and, with the increasing interlayer hydration, CO2 preferentially accumulates in interlamellar voids. The vibrational spectra produced by the new model, assuming that clay systems can exist in fractional hydration states, show either a combination of undisturbed and red-shifted asymmetric-stretch modes or a broad peak consistent with the multiple smeared peaks, which explain the multi-mode features that have appeared

  4. Surface wettability and energy effects on the biological performance of poly-3-hydroxybutyrate films treated with RF plasma.

    PubMed

    Syromotina, D S; Surmenev, R A; Surmeneva, M A; Boyandin, A N; Nikolaeva, E D; Prymak, O; Epple, M; Ulbricht, M; Oehr, C; Volova, T G

    2016-05-01

    The surface properties of poly-3-hydroxybutyrate (P3HB) membranes were modified using oxygen and an ammonia radio-frequency (RF, 13.56MHz) plasma. The plasma treatment procedures used in the study only affected the surface properties, including surface topography, without inducing any significant changes in the crystalline structure of the polymer, with the exception being a power level of 250W. The wettability of the modified P3HB surfaces was significantly increased after the plasma treatment, irrespective of the treatment procedure used. It was revealed that both surface chemistry and surface roughness changes caused by the plasma treatment affected surface wettability. A treatment-induced surface aging effect was observed and resulted in an increase in the water contact angle and a decrease in the surface free energy. However, the difference in the water contact angle between the polymers that had been treated for 4weeks and the untreated polymer surfaces was still significant. A dependence between cell adhesion and proliferation and the polar component of the surface energy was revealed. The increase in the polar component after the ammonia plasma modification significantly increased cell adhesion and proliferation on biodegradable polymer surfaces compared to the untreated P3HB and the P3HB modified using an oxygen plasma. PMID:26952446

  5. The characteristics of treated zone processed by pulsed Nd-YAG laser surface remelting on hot work steel

    NASA Astrophysics Data System (ADS)

    Zhang, Zhihui; Lin, Pengyu; Cong, Dalong; Kong, Shuhua; Zhou, Hong; Ren, Luquan

    2014-12-01

    In this study, the surface of H13 steel was treated using laser surface remelting. Some important characteristics of the treated zone (biomimetic strengthening units) were investigated, e.g. size, cross-sectional morphology, microstructure and hardness as functions of average peak power density and effective peak power density. The results indicate that different combinations of average peak power density and effective peak power density could vary the appearance of cross-sectional morphology, microstructure and hardness. An appropriate range of EPPD for preparing the treated zone was acquired: 595-1448 W/mm2. In this range, the depth/width ratio of 0.31-0.47 and microhardness of 559-667 HV were obtained.

  6. Possible selective adsorption of enantiomers by Na-montmorillonite

    NASA Technical Reports Server (NTRS)

    Friebele, E.; Shimoyama, A.; Ponnamperuma, C.

    1981-01-01

    Racemic amino acids including (D,L) alpha-alamine, (D,L) alpha-aminobutyric acid, (D,L) valine, and (D,L) norvaline were incubated with Na-montmorillonite at 100% CEC at three hydrogen ion concentrations, and amino acid adsorption was determined by ion exchange chromatography. Enantiomers were analyzed by gas chromatography. Differences in the quantities of D and L enantiomers in any of the fractions was no larger than a few percent. Although a large difference in the adsorption of the amino acid enantiomers was not observed, the analysis may indicate a small preferential adsorption (0.5-2%) of L-amino acids by Na-montmorillonite.

  7. [In vivo study of bacterial invasion in root planed and citric acid treated radicular surfaces of periodontally involved human teeth].

    PubMed

    Ito, K; Arai, N; Otogoto, J; Murai, S

    1989-06-01

    The purpose of this study was to investigate whether plaque bacteria invade the exposed radicular dentin after root planing or chemical root treatment in vivo. Eighteen caries-free human periodontally involved teeth with hopeless prognoses were studied. Fourteen teeth were scaled and root planed with hand curette type scalers. The proximal surface of each treated tooth was designated as the RP surface. The remaining half of the proximal surface was treated with citric acid (pH 1.0) for 3 minutes and was designated as the CA surface. Four untreated teeth served as controls. After 4 weeks, the teeth were extracted, and were processed for light microscopy and for scanning electron microscopy concerning bacterial invasion into the supragingival radicular dentin. The following results were obtained. 1. Radicular cementum was present on most untreated tooth surfaces. However, bacteria were never seen in the dentinal tubules. 2. Bacterial invasion into the dentinal tubules was observed in five of the 10 proximal surfaces (50% of the RP surfaces) and in nine of the 10 proximal surfaces (90% of the CA surfaces). 3. The depth (9.5 +/- 24.1 microns vs 84.6 +/- 136.3 microns) and percentage (0.8 +/- 2.1% vs 20.3 +/- 17.3%) of bacterial invasion in the dentinal tubules of the RP surfaces was lower than that of the CA surfaces. 4. Cocci and short rods were present in the supragingival dentinal tubules. 5. Since CA surfaces may accelerate bacterial invasion the citric acid treatment might be harmful in patients with inadequate plaque control. PMID:2700200

  8. Study of Np(V) Sorption by Ionic Exchange on Na, K, Ca and Mg-Montmorillonite

    NASA Astrophysics Data System (ADS)

    Benedicto, A.; Begg, J.; Zhao, P.; Kersting, A. B.; Zavarin, M.

    2012-12-01

    The transport behavior of actinides in soil and ground water are highly influenced by clay minerals due to their ubiquity in the environment, reactivity and colloidal properties. Neptunium(V) has been introduced in the environment as a result of nuclear weapons testing [e.g. 1, 2] and is a radionuclide of potential interest for safety assessment of high level radioactive waste disposal because its long half-life and high toxicity [3]. Surface complexation and ionic exchange have been identified as Np(V) sorption mechanisms onto montmorillonite. At pH below 5, Np(V) sorption is mainly attributed to ionic exchange. This study examines Np(V) ion exchange on Na, K, Ca and Mg forms of montmorillonite. Experiments were carried out using 237Np concentrations between 2 x 10-8 M and 5 x 10-6 M at three different ionic strengths 0.1, 0.01 and 0.001M. The pH was maintained at 4.5. Np(V) sorption to montmorillonite homoionized with monovalent cations (Na and K) demonstrated a markedly different behavior to that observed for montmorillonite homoionized with divalent cations (Ca and Mg). Np sorption to Na and K-montmorillonite was greater than Np sorption to Ca and Mg-montmorillonite. Isotherms with Na and K-montmorillonite showed a strong dependence on ionic strength: the percentage of Np adsorbed was near zero at 0.1M ionic strength, but increased to 30% at 0.001 M ionic strength. This suggests ionic exchange is the main Np adsorption mechanism under the experimental conditions investigated. Dependence on ionic strength was not observed in the Np sorption isotherms for Ca and Mg-montmorillonite indicating a low exchange capacity between Np and divalent cations. Modeling of the sorption experimental data will allow determination of the Na+↔NpO2+ and K+↔NpO2+ ionic exchange constants on montmorillonite. References: [1] A. R. Felmy; K. J. Cantrell; S. D. Conradson, Phys. Chem. Earth 2010, 35, 292-297 [2] D. K. Smith; D. L. Finnegan; S. M. Bowen, J. Environ. Radioact. 2003, 67

  9. A comparative study and evaluation of sulfamethoxazole adsorption onto organo-montmorillonites.

    PubMed

    Lu, Laifu; Gao, Manglai; Gu, Zheng; Yang, Senfeng; Liu, Yuening

    2014-12-01

    Three organo-montmorillonites were prepared using surfactants, and their adsorption behaviors toward sulfamethoxazole (SMX) were investigated. The surfactants used were cetyltrimethyl ammonium bromide (CTMAB), 3-(N,N-dimethylhexadecylammonio) propane sulfonate (HDAPS) and 1,3-bis(hexadecyldimethylammonio)-propane dibromide (BHDAP). The properties of the organo-montmorillonites were characterized by X-ray diffraction, scanning electron microscopy and N2 adsorption-desorption isotherm measurements. Results showed that the interlayer spacing of montmorillonite was increased and the surface area as well as the morphology were changed. Batch adsorption experiments showed that the surfactant loading amount had a great effect on the adsorption of SMX. The adsorption process was pH dependent and the maximum adsorption capacity was obtained at pH3 for HDAPS-Mt, while CTMAB-Mt and BHDAP-Mt showed a high removal efficiency at 3-11. The adsorption capacity increased with the initial SMX concentration and contact time but decreased with increasing solution ionic strength. Kinetic data were best described by the pseudo second-order model. Equilibrium data were best represented by the Langmuir model, and the Freundlich constant (n) indicated a favorable adsorption process. The maximum adsorption capacity of SMX was 235.29 mg/g for CTMAB-Mt, 155.28 mg/g for HDAPS-Mt and 242.72 mg/g for BHDAP-Mt. Thermodynamic parameters were calculated to evaluate the spontaneity and endothermic or exothermic nature. The adsorption mechanism was found to be dominated by electrostatic interaction, while hydrophobic interaction played a secondary role. PMID:25499502

  10. Uranium uptake by hectorite and montmorillonite: a solution chemistry and polarized EXAFS study.

    PubMed

    Schlegel, Michel L; Descostes, Michael

    2009-11-15

    The mechanism of U(VI) retention on montmorillonite and hectorite at high ionic strength (0.5 M NaCl) was investigated by solution chemistry and, at near-neutral pH, polarized EXAFS spectroscopy. Uranium(VI) sorption increases from pH 3 to 7 on the two clays, but with a steeper edge for hectorite. Uranium(VI) is no longer retained at pH > 9, presumably owing to the formation of soluble anionic complexes. Polarized EXAFS showed that U(VI) retains its uranyl conformation on montmorillonite (U_mont) and hectorite (U_hect), with uranyl O at 1.79(2) A for U_mont and 1.82(2) A for U_hect, and split equatorial O shells at 2.29(2) and 2.47(2) A (U_mont), or 2.35(2) and 2.53(2) A (U_hect). An additional atomic shell of approximately 0.5 Al/Si at 3.3 A is detected for U_mont, but neither the oxygen nor the cationic shell exhibit clear angular dependence. These results indicate the formation of mononuclear complexes at the edges of montmorillonite platelets, with the orientation of the uranyl axis equal to the magic angle, as constrained by the edges' structural properties. In contrast to U_mont, the U-O signal varies with the polarization angle in U_hect, and the cationic Mg/Si contribution at 3.2 A is weak. The structure of this surface complex is not completely elucidated; it may correspond either to sorption on silanol sites, or to coprecipitation. These results lay out the fundamental molecular-scale basis to understand U retention by neoformed clay layers of nuclear glasses. PMID:20028057

  11. Effect of phosphate on U(VI) sorption to montmorillonite: Ternary complexation and precipitation barriers

    NASA Astrophysics Data System (ADS)

    Troyer, Lyndsay D.; Maillot, Fabien; Wang, Zheming; Wang, Zimeng; Mehta, Vrajesh S.; Giammar, Daniel E.; Catalano, Jeffrey G.

    2016-02-01

    Phosphate addition is a potential treatment method to lower the solubility of U(VI) in soil and groundwater systems by causing U(VI) phosphate precipitation as well as enhancing adsorption. Previous work has shown that iron oxide surfaces may facilitate the nucleation of U(VI) phosphate minerals and, that under weakly acidic conditions, phosphate also enhances U(VI) adsorption to such phases. Like iron oxides, clays are important reactive phases in the subsurface but little is known about the interaction of U(VI) and phosphate with these minerals. The effect of aqueous phosphate on U(VI) binding to Wyoming montmorillonite (SWy-2) in air-equilibrated systems was investigated. Equilibrium U(VI) uptake to montmorillonite was determined at pH 4, 6 and 8 at discrete initial phosphate concentrations between 0 and 100 μM. The observed behavior of U(VI) indicates a transition from adsorption to precipitation with increasing total uranium and phosphate concentrations at all pH values. At the highest phosphate concentration examined at each pH value, a barrier to U(VI) phosphate nucleation is observed. At lower concentrations, phosphate has no effect on macroscopic U(VI) adsorption. To assess the mechanisms of U(VI)-phosphate interactions on smectite surfaces, U(VI) speciation was investigated under selected conditions using laser-induced fluorescence spectroscopy (LIFS) and extended X-ray absorption fine-structure (EXAFS) spectroscopy. Samples above the precipitation threshold display EXAFS and LIFS spectral signatures consistent with the autunite family of U(VI) phosphate minerals. However, at lower U(VI) concentrations, changes in LIFS spectra upon phosphate addition suggest that U(VI)-phosphate ternary surface complexes form on the montmorillonite surface at pH 4 and 6 despite the lack of a macroscopic effect on adsorption. The speciation of solid-associated U(VI) below the precipitation threshold at pH 8 is dominated by U(VI)-carbonate surface complexes. This work

  12. Mechanical properties of the sodium montmorillonite interlayer intercalated with amino acids.

    PubMed

    Katti, Dinesh R; Ghosh, Pijush; Schmidt, Steven; Katti, Kalpana S

    2005-01-01

    Nanosized montmorillonite clay dispersed in small amounts in polymer results in polymer nanocomposites having superior engineering properties compared to those of the native polymer. These nanoinclusions are created by treating clay with an organic modifier which makes clay organophilic and results in intercalation or exfoliation of the montmorillonite. The modifiers used are usually long carbon chains with alkylammonium or alkylphosphonium cations. In this work, we have investigated the use of some alternative molecules which can act as modifiers for clay composites using clay for reinforcing a matrix of biopeptides or proteins. Such composites have potential applications in the fields of biomedical engineering and pharmaceutical science. In this work, the amino acids arginine and lysine are used as modifiers. The intercalation and mechanical behavior of the interlayer spacing with these amino acids as inclusions under compression and tension are studied using molecular dynamics simulations. Significant differences in the responses are observed. This work also provides an insight into the orientation and interaction of amino acids in the interlayer under different stress paths. PMID:16283756

  13. Hexadimethrine-montmorillonite nanocomposite: Characterization and application as a pesticide adsorbent

    NASA Astrophysics Data System (ADS)

    Gámiz, B.; Hermosín, M. C.; Cornejo, J.; Celis, R.

    2015-03-01

    The goal of this work was to prepare and characterize a novel functional material by the modification of SAz-1 montmorillonite with the cationic polymer hexadimethrine (SA-HEXAD), and to explore the potential use of this nanocomposite as a pesticide adsorbent. Comparative preparation and characterization with the well-known hexadecyltrimethylammonium-modified SAz-1 montmorillonite (SA-HDTMA) was also assessed. The characterization was performed by elemental analysis, X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), physisorption of N2, scanning electron microscopy (SEM) and Z potential measurements. The characterization and adsorption experiments showed that the extent of pesticide adsorption was markedly subjected to the structure and features of the surface of each organo-clay and also to the nature of the considered pesticide. SA-HEXAD displayed a high affinity for anionic pesticides which, presumably, were adsorbed by electrostatic attraction on positively-charged ammonium groups of the polymer not directly interacting with the clay. In contrast, SA-HDTMA displayed great adsorption of both uncharged and anionic pesticides with predominance of hydrophobic interactions. This work provided information about the surface properties of a new organic-inorganic nanohybrid material, SA-HEXAD, and its potential as an adsorbent for the removal of anionic organic pollutants from aqueous solutions.

  14. Synergistic effect of cationic and anionic surfactants for the modification of Ca-montmorillonite

    SciTech Connect

    Zhang, Zepeng; Zhang, Jichu; Liao, Libing; Xia, Zhiguo

    2013-05-15

    Highlights: ► The basal spacing of MMT–CTAB–SDS reaches 5.30 nm. ► MMT–CTAB–SDS shows perfect dispersion property and excellent heat resistance. ► SDS helped to improve the heat resistance and decrease the surface energy of the MMT–CTAB–SDS particles. - Abstract: The synergistic effect of cationic surfactant (CTAB) and anionic surfactant (SDS) for the modification of Ca-montmorillonite (Ca-MMT) has been developed, and the novel cation–anion modified organomontmorillonite (MMT–CTAB–SDS) was prepared. X-ray diffraction (XRD) analysis indicates that the interlayer spacing of montmorillonite was well expanded by the intercalation of CTAB and SDS and the basal spacing increased from 1.54 nm (Ca-MMT) to 5.30 nm (MMT–CTAB–SDS). Thermogravimetric analysis (TG) showed that the MMT–CTAB–SDS displayed excellent heat resistance. Scanning electron microscopy (SEM) analysis proved that the MMT–CTAB–SDS exhibited excellent dispersion property and the plates with few silicate layers can be observed. Contact angle tests indicated that the hydrophilicity of MMT–CTAB–SDS was lower than that of Ca-MMT and higher than that of MMT–CTAB. It was verified that SDS contributed to expanding the interlayer space, further improved the heat resistance of the MMT–CTAB and decreased the surface energy of the MMT–CTAB–SDS particles.

  15. PARAMETERS OF TREATED STAINLESS STEEL SURFACES IMPORTANT FOR RESISTANCE TO BACTERIAL CONTAMINATION

    EPA Science Inventory

    Use of materials that are resistant to bacterial contamination could enhance food safety during processing. Common finishing treatments of stainless steel surfaces used for components of poultry processing equipment were tested for resistance to bacterial attachment. Surface char...

  16. Influence of Ca2+ on tetracycline adsorption on montmorillonite.

    PubMed

    Parolo, M Eugenia; Avena, Marcelo J; Pettinari, Gisela R; Baschini, Miria T

    2012-02-15

    The adsorption of tetracycline (TC) on montmorillonite was studied as a function of pH and Ca(2+) concentration using a batch technique complemented with X-ray diffraction and transmission electron microscopy. In the absence of Ca(2+), TC adsorption was high at low pH and decreased as the pH increased. In the presence of Ca(2+), at least two different adsorption processes took place in the studied systems, i.e., cation exchange and Ca-bridging. Cation exchange was the prevailing process at pH<5, and thus, TC adsorption decreased by increasing total Ca(2+) concentration. On the contrary, Ca-bridging was the prevailing process at pH>5, and thus, TC adsorption increased by increasing Ca(2+) concentration. The pH 5 represents an isoadsorption pH where both adsorption processes compensate each other. TC adsorption became independent of Ca(2+) concentration at this pH. For TC adsorption on Ca(2+)-montmorillonite in 0.01 M NaCl experiments, the ratio adsorbed TC/retained Ca(2+) was close to 1 in the pH range of 5-9, indicating an important participation of Ca(2+) in the binding of TC to montmorillonite. X-ray diffraction and transmission electron microscopy showed that TC adsorption induced intercalation between montmorillonite layers forming a multiphase system with stacking of layers with and without intercalated TC. PMID:22189389

  17. Modeling of alkyl quaternary ammonium cations intercalated into montmorillonite lattice

    SciTech Connect

    Daoudi, El Mehdi; Boughaleb, Yahia; El Gaini, Layla; Meghea, Irina; Bakasse, Mina

    2013-05-15

    Highlights: ► The modification of montmorillonites by three surfactants increases the basal spacing. ► The model proposed show a bilayer conformation for the surfactant ODTMA. ► The DODMA and TOMA surfactants adopt a paraffin type arrangement. ► Behavior of surfactants in interlayer space was confirmed by TGA and ATR analysis. - Abstract: The objective of this work was to study the conformation of the quaternary ammonium cations viz., octadecyl trimethyl ammonium (ODTMA), dioctadecyl dimethyl ammonium (DMDOA) and trioctadecyl methyl ammonium (TOMA) intercalated within montmorillonite. The modified montmorillonite was characterized by X-ray diffraction in small angle (SAXS), thermal analysis (TGA) and infrared spectroscopy of attenuated total reflection (ATR). The modification of organophilic montmorillonites by the three surfactants ODTMA, DMDOA and TOMA increases the basal spacing from their respective intercalated distances of 1.9 nm, 2.6 nm and 3.4 nm respectively. The increase in the spacing due to the basic organic modification was confirmed by the results of thermal analysis (TGA) and infrared spectroscopy (ATR), and also supported by theoretical calculations of longitudinal and transversal chain sizes of these alkyl quaternary ammonium cations.

  18. Effect of adsorbed iron on thermoluminescence and electron spin resonance spectra of Ca-Fe-exchanged montmorillonite

    NASA Technical Reports Server (NTRS)

    Coyne, Lelia M.; Banin, Amos

    1986-01-01

    The ESR spectra and the natural and gamma-induced thermoluminescence (TL) glow curves of a series of variably cation-exchanged Fe-Ca-clays prepared from SWy-1 montmorillonite were examined. The ESR signal intensity associated with surface Fe increased linearly with surface Fe content up to a nominal concentration of 50 percent exchangeable Fe. At above 50 percent exchangeable Fe, no appreciable increase in the signal was noted. The TL intensity decreased linearly with increasing surface Fe up to 50 percent nominal exchangeable Fe. At above 50 percent, the signal was not appreciably further diminished. Possible effects of Fe on quenching of TL are considered.

  19. Characteristics of TiO2 Thin Film Surfaces Treated by Helium and Air Dielectric Barrier Discharge Plasmas

    NASA Astrophysics Data System (ADS)

    Kawakami, Retsuo; Niibe, Masahito; Takeichi, Atsushi; Mori, Yuta; Konishi, Masashi; Kotaka, Takuya; Matsunaga, Fumihiko; Takasaki, Toshihide; Kitano, Takanori; Miyazaki, Takahiro; Inaoka, Takeshi; Tominaga, Kikuo

    2012-08-01

    The characteristics of TiO2 thin film surfaces treated with He and air dielectric barrier discharge (DBD) plasmas at different gas pressures are investigated. There is a difference between the two DBD plasma characteristics: for He-DBD, which is an atmospheric pressure glow discharge (APGD), the breakdown voltage and discharge current hardly change with increasing gas pressure, whereas for air-DBD, which is basically a filamentary discharge, they increase with increasing gas pressure. There is also a difference between the characteristics of TiO2 surfaces treated with the two DBDs. The surface roughness for He-DBD is lower than the roughness of the as-grown surface, whereas that for air-DBD is higher. The surface hydrophilicity for He-DBD is more enhanced than the hydrophilicity of the as-grown surface regardless of UV irradiation. The hydrophilicity for air-DBD is dependent on UV irradiation. It is more enhanced with UV irradiation; it is not improved adequately without UV irradiation.

  20. Morphology and Structure of Amino-fatty Acid Intercalated Montmorillonite

    NASA Astrophysics Data System (ADS)

    Reyes, Larry; Sumera, Florentino

    2015-04-01

    Natural clays and its modified forms have been studied for their wide range of applications, including polymer-layered silicate, catalysts and adsorbents. For nanocomposite production, montmorillonite (MMT) clays are often modified with organic surfactants to favor its intermixing with the polymer matrix. In the present study, Na+-montmorillonite (Na+-MMT) was subjected to organo-modification with a protonated 12-aminolauric acid (12-ALA). The amount of amino fatty acid surfactants loaded was 25, 50, 100 and 200% the cation exchange capacity (CEC) of Na+-MMT (25CEC-AMMT, 50CEC-AMMT, 100CEC-AMMT and 200CEC-AMMT). Fatty acid-derived surfactants are an attractive resource of intercalating agents for clays due to their renewability and abundance. X-ray diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FTIR) were performed to determine the occurrence of intercalation of 12-ALA and their molecular structure in the clay's silicates. XRD analysis revealed that the interlayer spacing between the alumino-silicate layers increased from 1.25 nm to 1.82 nm with increasing ALA content. The amino fatty acid chains were considered to be in a flat monolayer structure at low surfactant loading, and a bilayered to a pseudotrilayered structure at high surfactant loading. On the other hand, FTIR revealed that the alkyl chains adopt a gauche conformation, indicating their disordered state based on their CH2symmetric and asymmetric vibrations. Thermogravimetric analyses (TGA) allows the determination of the moisture and organic content in clays. Here, TGA revealed that the surfactant in the clay was thermally stable, with Td ranging from 353° C to 417° C. The difference in the melting behavior of the pristine amino fatty acids and confined fatty acids in the interlayer galleries of the clay were evaluated by Differential Scanning Calorimerty (DSC). The melting temperatures (Tm) of the amino fatty acid in the clay were initially found to be higher than those of the free

  1. A comparative study of the acidity toward the aqueous phase and adsorptive properties of Al{sub 13}-pillared montmorillonite and Al{sub 13}-pillared saponite

    SciTech Connect

    Bergaoui, L.; Mrad, I.; Ghorbel, A.; Lambert, J.F.

    1999-04-15

    The selectivity of an Al{sub 13}-pillared saponite and an Al{sub 13}-pillared montmorillonite for Cd{sup 2+} and Cu{sup 2+} adsorption was studied. The quantity of metal adsorbed on both pillared clays depends on the pH of the solution and the pillars density. Adsorption equilibria are regulated by the protonation equilibria of the amphoteric sites on the pillars. Pillared clays adsorb more cadmium and copper than classic aluminum hydroxides which is simply attributable to a higher density of surface aluminum groups. Significant differences in behavior are observed between pillared montmorillonite and pillared saponite. Pillared montmorillonite appears to be more acidic, which is correlated with a more advanced degree of structural modification of the pillars on calcination. The authors propose a tentative, partial structural model of pillar transformation compatible with these differences. At the same time, both pillared clays have similar affinities for cadmium II at low pH (5--6), but pillared montmorillonite seems to be a more efficient cadmium trap at pH = 8 when its surface groups are negatively ionized. Thus, the nature of the clay layers conditions the structural modifications of the intercalated [Al{sub 13}] polycations, which in turn determine adsorptive behavior.

  2. Characterization of wet-chemically treated silicon interfaces by surface photovoltage measurements.

    PubMed

    Angermann, H

    2002-10-01

    A non-destructive and surface-sensitive surface photovoltage (SPV) technique was employed to investigate the influence of important wet-chemical treatments on the electronic surface properties. The preparation-induced surface roughness as well as the hydrogen and oxide coverage were additionally determined by spectroscopic ellipsometry (SE). High values of interface charge and a high density of rechargeable interface states were observed on atomically rough surfaces and interfaces after HF-treatment and conventional wet-chemical oxidation. Both interface charge and density of rechargeable interface states could be reduced significantly by preparing an atomically flat Si surface and a well-ordered silicon/silicon oxide interface by applying special H-termination and hot-water oxidation procedures. PMID:12397491

  3. The effects of oil on As(V) adsorption on illite, kaolinite, montmorillonite and chlorite

    NASA Astrophysics Data System (ADS)

    Wainipee, Wimolporn; Cuadros, Javier; Sephton, Mark A.; Unsworth, Catherine; Gill, Martin G.; Strekopytov, Stanislav; Weiss, Dominik J.

    2013-11-01

    The effect of oil on As(V) adsorption on clay minerals has been investigated using batch experiments at low and high pH, NaCl concentration and oil contents. Four clay minerals were chosen because of their abundance in sediments and their different crystal chemistry: illite, kaolinite, montmorillonite, and chlorite. The values for pH were 4 and 8 and salt concentrations were 0.001 and 0.7 M NaCl to appreciate the effects of changing salinity, e.g. from fresh water to seawater conditions. For the coating experiments, a well-characterised oil was used to survey the main effects of complex organic mixtures on adsorption and oil to clay mineral (w/w) ratios were 0.0325 and 0.3250. As(V) adsorption increased with increasing NaCl concentration, suggesting that the mechanisms of As(V) adsorption are related to the formation of surface complexes in which Na+ ions act as bridges between the clay surface and the As(V) anions. Cation bridging is also indicated by zeta potential measurements which show that higher NaCl concentrations along with the presence of As(V) can cause the clay particles and adsorbed ions to have a more negative overall charge. Adsorption is lower at higher pH due to the reduced number of positively charged sites on the edge of clay mineral layers. Oil coating reduces As(V) adsorption by decreasing the available surface area of clay minerals, except in the case of oil-coated montmorillonite, where surface area following dispersion in water is increased. The main variables controlling As(V) adsorption are surface area and surface charge density, as confirmed by a simplified quantitative model. These findings advance our ability to predict the effects of complex pollution events in various freshwater and marine settings.

  4. Monte Carlo study of the adsorption and aggregation of alkyltrimethylammonium chloride on the montmorillonite-water interface.

    PubMed

    Klebow, Birthe; Meleshyn, Artur

    2012-09-18

    Organically modified clays exhibit adsorption capacities for cations, anions, and nonpolar organic compounds, which make them valuable for various environmental technical applications. To improve the understanding of the adsorption processes, the molecular-scale characterization of the structures of organic aggregates assembled on the external basal surfaces of clay particles is essential. The focus of this Monte Carlo simulation study was on the effects of the surface coverage and the alkyl chain length n on the structures of alkyltrimethylammonium chloride ((C(n)TMA)Cl) aggregates assembled on the montmorillonite-water interface. We found that the amount of adsorbed C(n)TMA(+) ions is independent of the alkyl chain length and increases with the C(n)TMA(+) surface coverage. The C(n)TMA(+) ions predominantly adsorb as inner-sphere complexes; the fraction of outer-sphere adsorbed ions equals only about 10%. The conformational order of the C(n)TMA(+) alkyl chains substantially decreases with decreasing alkyl chain length. In agreement with previous experiments, the amount of C(n)TMA(+) ions that are aggregated at the mineral surface increases with increasing chain length. The maximum value of 0.66 C(n)TMA(+) adsorption complex per unit cell area of the clay surface considerably exceeds the amount of cations required to compensate the negative charge of the montmorillonite surface. Furthermore, in most of the studied systems, fractions of Na(+) surface cations remain adsorbed on montmorillonite. The resulting interfacial positive charge excess is counterbalanced by coadsorbed chloride ions forming ion pairs with both C(n)TMA(+) and Na(+). PMID:22894657

  5. Evidence for a strong correlation between the amount of surface carbon and the tribological behaviour of ion-treated steels

    NASA Astrophysics Data System (ADS)

    Faussemagne, A.; Benyagoub, A.

    1998-02-01

    Samples of 100Cr6-bearing steel were treated by different ion beams in order to study the evolution of their tribological properties. Complementary physico-chemical characterisation techniques give evidence for a strong correlation between the amount of surface carbon, whatever its origin (contamination, direct C implantation or ion beam mixing of a deposited carbon layer), and the reduction of the friction coefficient as well as the increase of the wear resistance. It is found that the friction coefficient is improved by a factor 5 and the wear volume by two orders of magnitude when the amount of surface carbon exceeds 1017 C cm-2.

  6. Nonequilibrium structural condition in the medical TiNi-based alloy surface layer treated by electron beam

    SciTech Connect

    Neiman, Aleksei A. Lotkov, Aleksandr I.; Meisner, Ludmila L. Semin, Viktor O.; Koval, Nikolai N.; Teresov, Anton D.

    2014-11-14

    The research is devoted to study the structural condition and their evolution from the surface to the depth of TiNi specimens treated by low-energy high-current electron beams with surface melting at a beam energy density E = 10 J/cm{sup 2}, number of pulses N = 10, and pulse duration τ = 50 μs. Determined thickness of the remelted layer, found that it has a layered structure in which each layer differs in phase composition and structural phase state. Refinement B2 phase lattice parameters in local areas showed the presence of strong inhomogeneous lattice strain.

  7. Sorption of chlorimuron-ethyl on montmorillonite clays: effects of exchangeable cations, pH, and ionic strength.

    PubMed

    Ren, Wenjie; Teng, Ying; Zhou, Qixing; Paschke, Albrecht; Schüürmann, Gerrit

    2014-10-01

    Sorption interaction of chlorimuron-ethyl with montmorillonite clays was investigated under varied types of exchangeable cation, pH, and ionic strength conditions. Chlorimuron-ethyl sorption on bentonites exhibited pronounced cation dependency, and the sorption ability increased as the sequence Ca(2+)- < Na(+)- < Al(3+)- < Fe(3+)-bentonite, due to different sorption mechanisms, whereas the cation dependency was influenced by the clay type and much weaker for montmorillonites. The decrease of pH at the range of 4.0-6.0 prominently increased sorption of chlorimuron-ethyl on all cation-exchanged montmorillonite clays, and nearly a neglected sorption (about 2 %) can be observed at pH over 7.0. In the presence of CaCl2, sorption of chlorimuron-ethyl on Fe(3+)-bentonite was promoted because of complexion of Ca(2+) and the surface of Fe(3+)-bentonite. However, as the concentration of CaCl2 increased, chlorimuron-ethyl sorption on Ca(2+)- and Fe(3+)-exchanged bentonite decreased, suggesting that Ca bridging was not the prevailing mechanism for sorption of chlorimuron-ethyl on these clays. Furthermore, chlorimuron-ethyl sorption was relatively sensitive to pH, and the change of pH may obscure effect of other factors on the sorption, so it was quite necessary to control pH at a constant value when the effect of other factor was being studied. PMID:25028319

  8. Adsorption and degradation of model volatile organic compounds by a combined titania-montmorillonite-silica photocatalyst.

    PubMed

    Chen, Jiangyao; Li, Guiying; He, Zhigui; An, Taicheng

    2011-06-15

    A series of adsorptive photocatalysts, combined titania-montmorillonite-silica were synthesized. The resultant photocatalysts consisted of more and more spherically agglomerated TiO(2) particles with increasing of TiO(2) content, and anatase was the only crystalline phase with nano-scale TiO(2) particles. With increasing of the cation exchange capacity to TiO(2) molar ratio, specific surface area and pore volume increased very slightly. In a fluidized bed photocatalytic reactor by choosing toluene, ethyl acetate and ethanethiol as model pollutants, all catalysts had relatively high adsorption capacities and preferred to adsorb higher polarity pollutants. Langmuir isotherm model better described equilibrium data compared to Freundlich model. Competitive adsorptions were observed for the mixed pollutants on the catalysts, leading to decrease adsorption capacity for each pollutant. The combined titania-montmorillonite-silica photocatalyst exhibited excellent photocatalytic removal ability to model pollutants of various components. Almost 100% of degradation efficiency was achieved within 120 min for each pollutant with about 500 ppb initial concentration, though the efficiencies of multi-component compounds slightly decreased. All photocatalytic reactions followed the Langmuir-Hinshelwood model. Degradation rate constants of multi-component systems were lower than those for single systems, following the order of toluene

  9. Morphological and surface studies of ultrasonically treated Raney nickel hydrogen-deuterium exchange catalysts

    SciTech Connect

    Cioffi, E.A. ); Willis, W.S.; Suib, S.L. )

    1990-02-01

    Previous surface studies of ultrasonicated Raney nickel catalysts have shown that ultrasonication leads to reduction of surface Ni species to the metallic state. Surface impurities that may poison the Raney nickel catalyst have also been removed during ultrasonication. Negligible increases in surface area are observed after ultrasound treatment of the catalysts even though their activities and selectivities in {sup 2}H incorporation into carbohydrates and glycosphingolipids are markedly improved. The surface and morphological changes taking place during ultrasonic treatment are the focus of this paper. Cr{sup 3+}- and Mo{sup 6+}-doped Raney Ni catalysts have been studied before and after ultrasonciation with scanning electron microscopy, X-ray photoelectron spectroscopy, and secondary ion mass spectrometry.

  10. Influence of laser surface treated on the characterization and corrosion behavior of Al-Fe aerospace alloys

    NASA Astrophysics Data System (ADS)

    Pariona, Moisés Meza; Teleginski, Viviane; dos Santos, Kelly; de Lima, Angela A. O. C.; Zara, Alfredo J.; Micene, Katieli Tives; Riva, Rudimar

    2013-07-01

    In this research laser surface remelting without protective coating with a 2 kW Yb-fiber laser (IPG YLR-2000S) was applied in the Al-1.5 wt.%Fe alloy in order to investigate the layer treated with different techniques of superficial characterization, thereby, the technique of optical microscopy, atomic force microscopy and low-angle X-ray diffraction were used. The present work mainly focuses on the corrosion study by diverse techniques in aggressive environment of the laser-treated area and the substrate material was carried out, thereby, at open circuit potential testing, the results have shown a displacement to more anodic values in the corrosion potential for the laser-treated specimen when compared to the untreated specimen; in potentiodynamic polarization tests have shown that as a result of the laser treatment, the corrosion current can be reduced by as much as ten times, and a passive region was obtained, which served as an effective barrier for reducing anodic dissolution and finally, the result in cyclic polarization curves of the untreated sample there was a greater area of the hysteresis loop, implying that it is more susceptible to corrosion. This study was complemented by other techniques mentioned above in order to elucidate this study. Laser surface remelting process has definitely modified the surface film, which results in higher corrosion resistance, a large range of passivation and a lower area of the hysteresis loop.