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Sample records for cationic surface modification

  1. Surface modification of cation exchange membranes by graft polymerization of PAA-co-PANI/MWCNTs nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Nemati, Mahsa; Hosseini, Sayed Mohsen; Bagheripour, Ehsan [Faculty of Engineering, Arak University, Arak (Iran, Islamic Republic of); Madaeni, Sayed Siavash [Faculty of Engineering, Razi University, Kermanshah (Iran, Islamic Republic of)

    2016-03-15

    Surface modification of polyvinylchloride based heterogeneous cation exchange membrane was performed by graft polymerization of PAA and PAA-co-PANI/MWCNTs nanoparticles. The ion exchange membranes were prepared by solution casting technique. Spectra analysis confirmed graft polymerization clearly. SEM images illustrated that graft polymerization covers the membranes by simple gel network entanglement. The membrane water content was decreased by graft polymerization of PAA-co-PANI/MWCNTs nanoparticles on membrane surface. Membrane transport number and selectivity declined initially by PAA graft polymerization and then began to increase by utilizing of composite nanoparticles in modifier solution. The sodium and barium flux was improved sharply by PAA and PAAco- 0.01%wt PANI/MWCNTs graft polymerization on membrane surface and then decreased again by more increase of PANI/MWCNTs nanoparticles content ratio in modifier solution. The electrodialysis experiment results in laboratory scale showed higher dialytic rate in heavy metals removal for grafted-PAA and grafted-PAA-co-PANI/MWCNTs modified membrane compared to pristine one. Membrane areal electrical resistance was also decreased by introducing graft polymerization of PAA and PAA-co-PANI/MWCNTs NPs on membrane surface.

  2. Cationic surface modification of PLG nanoparticles offers sustained gene delivery to pulmonary epithelial cells.

    Science.gov (United States)

    Baoum, Abdulgader; Dhillon, Navneet; Buch, Shilpa; Berkland, Cory

    2010-05-01

    Biodegradable polymeric nanoparticles are currently being explored as a nonviral gene delivery system; however, many obstacles impede the translation of these nanomaterials. For example, nanoparticles delivered systemically are inherently prone to adsorbing serum proteins and agglomerating as a result of their large surface/volume ratio. What is desired is a simple procedure to prepare nanoparticles that may be delivered locally and exhibit minimal toxicity while improving entry into cells for effectively delivering DNA. The objective of this study was to optimize the formulation of poly(D,L-lactide-co-glycolide) (PLG) nanoparticles for gene delivery performance to a model of the pulmonary epithelium. Using a simple solvent diffusion technique, the chemistry of the particle surface was varied by using different coating materials that adsorb to the particle surface during formation. A variety of cationic coating materials were studied and compared to more conventional surfactants used for PLG nanoparticle fabrication. Nanoparticles (approximately 200 nm) efficiently encapsulated plasmids encoding for luciferase (80-90%) and slowly released the same for 2 weeks. In A549 alveolar lung epithelial cells, high levels of gene expression appeared at day 5 for certain positively charged PLG particles and gene expression was maintained for at least 2 weeks. In contrast, PEI gene expression ended at day 5. PLG particles were also significantly less cytotoxic than PEI suggesting the use of these vehicles for localized, sustained gene delivery to the pulmonary epithelium.

  3. Modification of Nafion Membranes by IL-Cation Exchange: Chemical Surface, Electrical and Interfacial Study

    Directory of Open Access Journals (Sweden)

    V. Romero

    2012-01-01

    A study of time evolution of the impedance curves measured in the system “IL aqueous solution/Nafion-112 membrane/IL aqueous solution” was also performed. This study allows us monitoring the electrical changes associated to the IL-cation incorporation in both the membrane and the membrane/IL solution interface, and it provides supplementary information on the characteristic of the Nafion/DTA+ hybrid material. Moreover, the results also show the significant effect of water on the electrical resistance of the Nafion-112/IL-cation-modified membrane.

  4. Preparation and characterization of cationic Pluronic for surface modification and functionalization of polymeric drug delivery nanoparticles

    Directory of Open Access Journals (Sweden)

    G. Gyulai

    2016-03-01

    Full Text Available Biodegradable poly(lactic-co-glycolic acid copolymer, PLGA nanoparticles (NPs with a surface layer of poly (ethylene oxide-poly(propylene oxide-poly(ethylene oxide triblock copolymers, Pluronics, are promising drug carrier systems. With the aim to increase the potential of targeted drug delivery the end group derivative of Pluronics was synthesized in a straightforward way to obtain Pluronic-amines. The formation of functional amine groups was confirmed by fluorescamine method and NMR analysis of their N-(tert-Butoxycarbonyl-L-phenylalanine (Boc-Phe-OH and N-(9-Fluorenylmethoxycarbonyl-L-phenylalanine (Fmoc-Phe-OH conjugates. Pluronic and Pluronic-amine stabilized PLGA NPs prepared by nanoprecipitation were characterized by dynamic light scattering and zeta potential measurements. All of the systems showed high colloidal stability checked by electrolyte induced aggregation, although the presence of Pluronicamine on the surface decreased the zeta potential in some extent. The introduction of reactive primary amine groups into the surface layer of PLGA NPs while preserving the aggregation stability, provides a possibility for coupling of various ligands allowing targeted delivery and also contributes to the improved membrane affinity of NPs.

  5. Facile Use of Cationic Hydrogel Particles for Surface Modification of Planar Substrates Toward Multifunctional Neural Permissive Surfaces: An in Vitro Investigation.

    Science.gov (United States)

    Morin, Emily A; Tang, Shuangcheng; Rogers, Katie Lou; He, Wei

    2016-03-02

    Synthetic materials such as silicon have been commonly used for neural interfacing applications but are intrinsically noninteractive with neurons. Here, a facile approach has been developed to integrate both chemical and topographical cues to impart neural permissiveness for such materials. The approach simply exploits the basic phenomenon of electrostatically driven adsorption of colloidal particles onto a solid material and applies it to a cationic hydrogel particle system that we have developed recently based on "click" reaction of epoxide and amine. The particle adsorption process can be tuned by varying the adsorption time and the concentration of the original colloidal suspension, both of which directly control the surface densities of the adsorbed hydrogel particles. Using the PC12 cell line and primary cortical neurons derived from chick embryo, we demonstrate that the particle-adsorbed surface readily supports robust cell adhesion and differentiation. Although the extent of neural permissiveness exhibited by such particle-adsorbed surface was comparable to the cationic polyethylenimine-coated control surface, the adsorbed hydrogel particles offer a unique reservoir function to the modified surface that is unparalleled by the control. The successful loading of hydrophobic dye of nile red to the surface adsorbed hydrogel particles indicates that the modified surface not only provides physical support of neurons, but also can be explored in the future to exert localized therapeutic actions favorable for neural interfacing.

  6. Surface Modification of Multiwall Carbon Nanotubes with Cationic Conjugated Polyelectrolytes: Fundamental Interactions and Intercalation into Conductive Poly(methyl-methacrylate) Composites

    KAUST Repository

    Ezzeddine, Alaa

    2015-05-22

    This research investigates the modification and dispersion and of pristine multiwalled carbon nanotubes (MWCNTs) through a simple solution mixing technique based on noncovalent interactions between poly(phenylene ethynylene) based conjugated polyelectrolytes functionalized with cationic imidazolium solubilizing groups (PIM-2 and PIM-4) and MWCNTs. Spectroscopic studies demonstrated the ability of PIMs to strongly interact with and efficiently disperse MWCNTs in different solvents mainly due to π-interactions between the PIMs and MWCNTs. Transmission electron microscopy and atomic force microscopy revealed the coating of the polyelectrolytes on the walls of the nanotubes. Scanning electron microscopy (SEM) studies confirm the homogenous dispersion of PIM modified MWCNTs in poly(methyl methacrylate) (PMMA) matrix. The addition of 1 wt% PIM modified MWCNTs to the matrix has led to a significant decrease in DC resistivity of the composite (13 orders of magnitude). The increase in electrical conductivity and the improvement in thermal and mechanical properties of the membranes containing the PIM modified MWCNTs is ascribed to the formation of MWCNTs networks and cross-linking sites that provided channels for the electrons to move in throughout the matrix and reinforced the interface between MWCNTs and PMMA.

  7. Surface modification technology

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Wonbaek; Yu, Hyosin; Chung, Inwha; Rhee, Kang In; Choi, Good Sun; Lee, Chulkyung; Youn, In Ju; Chung, Jinki; Suh, Chang Youl; Yang, Dong Hyo [Korea Institute of Geology Mining and Materials, Taejon (Korea, Republic of)

    1997-12-01

    Domestic production of rare metals has not been achieved due to the low metal content in their ores in the nation. For these reasons, a strategy for the value addition of rare metal sponges by processes like vacuum melting should be seek to meet the growing domestic demand for titanium metals and alloys. However, current domestic market appears not to be sufficient enough for the large scale investment for the expensive vacuum-melting equipment. Besides, related ingot-processing technologies like rolling, extrusion, and forging of titanium should be prepared in advance. In the mean time, the attempt to recycle expensive titanium scraps produced in our nation would be worthwhile in view of the reduction of import from foreign countries and of saving valuable secondary resources. The objectives for this research is to develop a multipurpose inductively-coupled plasma enhanced-surface modification (ICPESM) process to upgrade powder products. Stable plasma was obtained by the impedance harmonization between plasma generator and matching networks maintaining the reflected power at near zero. The chamber vacuum went down to 10{sup -3} torr offering no difficulties to maintain 1.0 torr at which the present experiments were conducted. However, the fluidization in the chamber was unstable when operated in vacuum. The gas distributor and chamber design may need modifications. Argon plasma treatment on the titanium powders changed the surface morphology slightly even though the effect was not significant due possibly to the short treatment duration of 60 minutes. Oxygen plasma oxidized the surface of titanium powders to TiO{sub 2} as confirmed by XRD. The carbon black powders were clustered during oxidation treatment by the fluidization or surface activation by the high power of low temperature plasma. (author). 4 tabs., 15 figs.

  8. Surface modification of bioceramics

    Science.gov (United States)

    Monkawa, Akira

    Hydroxyapatite [Ca10(PO4)6(OH)2, HAp] is a major inorganic component of bone and teeth tissues and has the excellent biocompatibility and high osteoconductivity. The interactions between HAp and protein or cell have been studied. The HAp related bioceramics such as bone substitute, coating substance of metal implants, inorganic-polymer composites, and cell culture. We described two methods; (1) surface modification of HAp using organosilane; (2) fabrication of HAp ultra-thin layer on gold surface for protein adsorption analyzed with QCM-D technique. The interfacial interaction between collagen and HAp in a nano-region was controlled by depositing the organosilane of n-octadecyltrimethoxysilane (ODS: -CH3) or aminopropyltriethoxysilane (APTS: -NH2) with a chemical vapor deposition method. The morphologies of collagen adsorbed on the surfaces of HAp and HAp deposited with APTS were similar, however that of the surface with ODS was apparently different, due to the hydrophobic interaction between the organic head group of -CH3 and residual groups of collagen. We present a method for coating gold quartz crystal microbalance with dissipation (QCM-D) sensor with ultra-thin layer of hydroxyapatite nanocrystals evenly covering and tightly bound to the surface. The hydroxyapatite sensor operated in liquid with high stability and sensitivity. The in-situ adsorption mechanism and conformational change of fibrinogen on gold, titanium and hydroxyapatite surfaces were investigated by QCM-D technique and Fourier-transform infrared spectroscopy. The study indicates that the hydroxyapatite sensor is applicable for qualitative and conformational analysis of protein adsorption.

  9. Surface chemical modification of nanocrystals

    Energy Technology Data Exchange (ETDEWEB)

    Helms, Brett Anthony; Milliron, Delia Jane; Rosen, Evelyn Louise; Buonsanti, Raffaella; Llordes, Anna

    2017-03-14

    Nanocrystals comprising organic ligands at surfaces of the plurality of nanocrystals are provided. The organic ligands are removed from the surfaces of the nanocrystals using a solution comprising a trialkyloxonium salt in a polar aprotic solvent. The removal of the organic ligands causes the nanocrystals to become naked nanocrystals with cationic surfaces.

  10. Surface Modification of Intraocular Lenses

    Directory of Open Access Journals (Sweden)

    Qi Huang

    2016-01-01

    Full Text Available Objective: This paper aimed to review the current literature on the surface modification of intraocular lenses (IOLs. Data Sources: All articles about surface modification of IOLs published up to 2015 were identified through a literature search on both PubMed and ScienceDirect. Study Selection: The articles on the surface modification of IOLs were included, but those on design modification and surface coating were excluded. Results: Technology of surface modification included plasma, ion beam, layer-by-layer self-assembly, ultraviolet radiation, and ozone. The main molecules introduced into IOLs surface were poly (ethylene glycol, polyhedral oligomeric silsesquioxane, 2-methacryloyloxyethyl phosphorylcholine, TiO 2 , heparin, F-heparin, titanium, titanium nitride, vinyl pyrrolidone, and inhibitors of cytokines. The surface modification either resulted in a more hydrophobic lens, a more hydrophilic lens, or a lens with a hydrophilic anterior and hydrophobic posterior surface. Advances in research regarding surface modification of IOLs had led to a better biocompatibility in both in vitro and animal experiments. Conclusion: The surface modification is an efficient, convenient, economic and promising method to improve the biocompatibility of IOLs.

  11. Plasma surface modification of polymers

    Science.gov (United States)

    Hirotsu, T.

    1980-01-01

    Thin plasma polymerization films are discussed from the viewpoint of simplicity in production stages. The application of selective, absorbent films and films used in selective permeability was tested. The types of surface modification of polymers discussed are: (1) plasma etching, (2) surface coating by plasma polymerized thin films, and (3) plasma activation surface graft polymerization.

  12. Surface modification of cellulose nanocrystals

    Science.gov (United States)

    Eyley, Samuel; Thielemans, Wim

    2014-06-01

    Chemical modification of cellulose nanocrystals is an increasingly popular topic in the literature. This review analyses the type of cellulose nanocrystal modification reactions that have been published in the literature thus far and looks at the steps that have been taken towards analysing the products of the nanocrystal modifications. The main categories of reactions carried out on cellulose nanocrystals are oxidations, esterifications, amidations, carbamations and etherifications. More recently nucleophilic substitutions have been used to introduce more complex functionality to cellulose nanocrystals. Multi-step modifications are also considered. This review emphasizes quantification of modification at the nanocrystal surface in terms of degree of substitution and the validity of conclusions drawn from different analysis techniques in this area. The mechanisms of the modification reactions are presented and considered with respect to the effect on the outcome of the reactions. While great strides have been made in the quality of analytical data published in the field of cellulose nanocrystal modification, there is still vast scope for improvement, both in data quality and the quality of analysis of data. Given the difficulty of surface analysis, cross-checking of results from different analysis techniques is fundamental for the development of reliable cellulose nanocrystal modification techniques.

  13. Functionalised Polymers by Surface Modification

    Institute of Scientific and Technical Information of China (English)

    Jon-Paul Griffiths; M. G. Moloney

    2005-01-01

    @@ 1Introduction Surface-active polymers are of substantial importance in many diverse aspects of modern technology, with applications ranging from solid phase chemical synthesis related to drug discovery and chemical catalysis to biocompatible/bioactive medical implants and prostheses, and to surface-modified fabrics. Whilst there are a number of existing physical (e. g. corona or plasma discharge, ion beam irradiation[1] ) and chemical (e. g.silanisation, oxidation, chlorination, acylation and quaternisation[2-4]) methods for the surface modification of polymers, the frequent requirement for significant infrastructure, harsh reaction conditions, and limitation to specific polymer types (e. g. polybutadiene[5] ), which must possess suitable chemical functionality capable of direct modification, led us to consider alternative chemical methods. Desirable was an alternative that would be amenable to a large range of polymers, permitting direct chemical modification under mild conditions and using inexpensive reagents.

  14. Surface modification for corrosion resistance

    Energy Technology Data Exchange (ETDEWEB)

    Natesan, K.

    1993-06-01

    The raw gas environments that arise from coal gasification have chemical compositions that are low in pO{sub 2} and moderate-to-high in pS{sub 2}. Metallic materials for service in such an environment undergo predominantly sulfidation attack at temperatures of 400 to 700{degree}C. Modification of alloy compositions in bulk can alter the scaling processes and lead to improvements in corrosion resistance, but the benefits can only be attained at temperatures much higher than the service temperatures of the components. Modification of surfaces of structural components by several of the coating techniques examined in this study showed substantial benefit in corrosion resistance when tested in simulated coal gasification environments. The paper presents several examples of surface modification and their corrosion performance.

  15. Laser surface modification and adhesion

    CERN Document Server

    Mittal, K L

    2014-01-01

    The book provides a unique overview on laser techniques and applications for the purpose of improving adhesion by altering surface chemistry and topography/morphology of the substrate. It details laser surface modification techniques for a wide range of industrially relevant materials (plastics, metals, ceramics, composites) with the aim to improve and enhance their adhesion to other materials. The joining of different materials is of critical importance in the fabrication of many and varied products.

  16. Bordetella pertussis lipid A glucosamine modification confers resistance to cationic antimicrobial peptides and increases resistance to outer membrane perturbation.

    Science.gov (United States)

    Shah, Nita R; Hancock, Robert E W; Fernandez, Rachel C

    2014-08-01

    Bordetella pertussis, the causative agent of whooping cough, has many strategies for evading the human immune system. Lipopolysaccharide (LPS) is an important Gram-negative bacterial surface structure that activates the immune system via Toll-like receptor 4 and enables susceptibility to cationic antimicrobial peptides (CAMPs). We show modification of the lipid A region of LPS with glucosamine increased resistance to numerous CAMPs, including LL-37. Furthermore, we demonstrate that this glucosamine modification increased resistance to outer membrane perturbation.

  17. Energy conservation potential of surface modification technologies

    Energy Technology Data Exchange (ETDEWEB)

    Le, H.K.; Horne, D.M.; Silberglitt, R.S.

    1985-09-01

    This report assesses the energy conservation impact of surface modification technologies on the metalworking industries. The energy conservation impact of surface modification technologies on the metalworking industries is assessed by estimating their friction and wear tribological sinks and the subsequent reduction in these sinks when surface modified tools are used. Ion implantation, coatings, and laser and electron beam surface modifications are considered.

  18. Surface Modification for Microreactor Fabrication

    Directory of Open Access Journals (Sweden)

    Wladyslaw Torbicz

    2006-04-01

    Full Text Available In this paper, methods of surface modification of different supports, i.e. glass andpolymeric beads for enzyme immobilisation are described. The developed method ofenzyme immobilisation is based on Schiff’s base formation between the amino groups onthe enzyme surface and the aldehyde groups on the chemically modified surface of thesupports. The surface of silicon modified by APTS and GOPS with immobilised enzymewas characterised by atomic force microscopy (AFM, time-of-flight secondary ion massspectroscopy (ToF-SIMS and infrared spectroscopy (FTIR. The supports withimmobilised enzyme (urease were also tested in combination with microreactors fabricatedin silicon and Perspex, operating in a flow-through system. For microreactors filled withurease immobilised on glass beads (Sigma and on polymeric beads (PAN, a very high andstable signal (pH change was obtained. The developed method of urease immobilisationcan be stated to be very effective.

  19. Characterization of Surface Modification of Polyethersulfone Membrane

    Science.gov (United States)

    Surface modification of polyethersulfone (PES) membrane surface using UV/ozone-treated grafting and interfacial polymerization on membrane surface was investigated in order to improve the resistance of membrane surface to protein adsorption. These methods of surface modification were compared in te...

  20. Surface modification of cellulose nanocrystals

    Institute of Scientific and Technical Information of China (English)

    WANG Neng; DING Enyong; CHENG Rongshi

    2007-01-01

    In order to improve the dispersibility of cellulose nanocrystal(CNC) particles,three difierent grafted reactions of acetylation,hydroxyethylation and hydroxypropylation were introduced to modify the CNC surface.The main advantages of these methods were the simple and easily controlled reaction conditions,and the dispersibility of the resulting products was distinctly improved.The properties of the modified CNC were characterized by means of Fourier transform infrared spectroscopy(FT-IR),13 C nuclear magnetic resonance(NMR),transmission electron microscopy(TEM)and thermogravimetric analyses(TGA).The results indicated mat after desiccation,the modification products could be dispersed again in the proper solvents by ultrasonic treatments,and the diameter of their particles had no obvious changes.However,their thermal degradation behaviors were quite different.The initial decomposition temperature of the modified products via hydroxyethylation or hydroxypropylation was lower than that of modified products via acetylation.

  1. Surface modification using ionic liquid ion beams

    Energy Technology Data Exchange (ETDEWEB)

    Takaoka, Gikan H.; Hamaguchi, Takuya; Takeuchi, Mitsuaki; Ryuto, Hiromichi

    2014-12-15

    We developed an ionic liquid (IL) ion source using 1-butyl-3-methylimidazolium hexafluorophosphate (BMIM-PF{sub 6}) and produced IL ion beams by applying a high electric field between the tip and the extractor. Time-of-flight measurements showed that small cluster and fragment ions were contained in the positive and negative ion beams. The positive and negative cluster ions were deposited on Si(1 0 0) substrates. X-ray photoelectron spectroscopy measurements showed that the composition of the deposited layers was similar to that of an IL solvent. This suggests that a cation (A{sup +}) or an anion (B{sup −}) was attached to an IL cluster (AB){sub n}, resulting in the formation of positive cluster ions (AB){sub n}A{sup +} or negative cluster ions (AB){sub n}B{sup −}, respectively. The surfaces of the IL layers deposited on Si(1 0 0) substrates were flat at an atomic level for positive and negative cluster ion irradiation. Moreover, the contact angles of the deposited layers were similar to that of the IL solvent. Thus, surface modification of Si(1 0 0) substrates was successfully demonstrated with BMIM-PF{sub 6} cluster ion beams.

  2. Surface modification to prevent oxide scale spallation

    Science.gov (United States)

    Stephens, Elizabeth V; Sun, Xin; Liu, Wenning; Stevenson, Jeffry W; Surdoval, Wayne; Khaleel, Mohammad A

    2013-07-16

    A surface modification to prevent oxide scale spallation is disclosed. The surface modification includes a ferritic stainless steel substrate having a modified surface. A cross-section of the modified surface exhibits a periodic morphology. The periodic morphology does not exceed a critical buckling length, which is equivalent to the length of a wave attribute observed in the cross section periodic morphology. The modified surface can be created using at least one of the following processes: shot peening, surface blasting and surface grinding. A coating can be applied to the modified surface.

  3. Silica surfaces lubrication by hydrated cations adsorption from electrolyte solutions.

    Science.gov (United States)

    Donose, Bogdan C; Vakarelski, Ivan U; Higashitani, Ko

    2005-03-01

    Adsorption of hydrated cations on hydrophilic surfaces has been related to a variety of phenomena associated with the short-range interaction forces and mechanisms of the adhesive contact between the surfaces. Here we have investigated the effect of the adsorption of cations on the lateral interaction. Using lateral force microscopy (LFM), we have measured the friction force between a silica particle and silica wafer in pure water and in electrolyte solutions of LiCl, NaCl, and CsCl salts. A significant lubrication effect was demonstrated for solutions of high electrolyte concentrations. It was found that the adsorbed layers of smaller and more hydrated cations have a higher lubrication capacity than the layers of larger and less hydrated cations. Additionally, we have demonstrated a characteristic dependence of the friction force on the sliding velocity of surfaces. A mechanism for the observed phenomena based on the microstructures of the adsorbed layers is proposed.

  4. Modification of the cation exchange resin properties by impregnation in polyethyleneimine solutions: application to the separation of metallic ions.

    Science.gov (United States)

    Amara, Mourad; Kerdjoudj, Hacène

    2003-07-27

    A commercial cation exchange resin Amberlite 200 has been modified after immersion in solutions of polyethyleneimine (PEI). The kinetic of fixation of the metallic ions have been determined. The modification of the surface of the resin deals with a change in the order of the affinities of the resins towards cations. The retention is the function of the formation and the stability of the complex. The conditions of modification (pH, PEI concentration and time of immersion) have been examined and the modification was confirmed by the determination of the exchange capacities, the distribution coefficient (P) and the selectivity factors (S). The obtained results revealed the effect of PEI on the exchange properties of the resin. The pH range selected (6-8) permitted a good adherence of PEI onto the resin surface. The quantity of the adsorbed PEI was increased by raising the initial concentration and the immersion period. The exchange capacity for copper ion passed from 2.6 mmol g(-1), in the case of unmodified resin, to 3.9 mmol g(-1) for the modified one.

  5. Modulating macrophage polarization with divalent cations in nanostructured titanium implant surfaces

    Science.gov (United States)

    Lee, Chung-Ho; Kim, Youn-Jeong; Jang, Je-Hee; Park, Jin-Woo

    2016-02-01

    Nanoscale topographical modification and surface chemistry alteration using bioactive ions are centrally important processes in the current design of the surface of titanium (Ti) bone implants with enhanced bone healing capacity. Macrophages play a central role in the early tissue healing stage and their activity in response to the implant surface is known to affect the subsequent healing outcome. Thus, the positive modulation of macrophage phenotype polarization (i.e. towards the regenerative M2 rather than the inflammatory M1 phenotype) with a modified surface is essential for the osteogenesis funtion of Ti bone implants. However, relatively few advances have been made in terms of modulating the macrophage-centered early healing capacity in the surface design of Ti bone implants for the two important surface properties of nanotopography and and bioactive ion chemistry. We investigated whether surface bioactive ion modification exerts a definite beneficial effect on inducing regenerative M2 macrophage polarization when combined with the surface nanotopography of Ti. Our results indicate that nanoscale topographical modification and surface bioactive ion chemistry can positively modulate the macrophage phenotype in a Ti implant surface. To the best of our knowledge, this is the first demonstration that chemical surface modification using divalent cations (Ca and Sr) dramatically induces the regenerative M2 macrophage phenotype of J774.A1 cells in nanostructured Ti surfaces. In this study, divalent cation chemistry regulated the cell shape of adherent macrophages and markedly up-regulated M2 macrophage phenotype expression when combined with the nanostructured Ti surface. These results provide insight into the surface engineering of future Ti bone implants that are harmonized between the macrophage-governed early wound healing process and subsequent mesenchymal stem cell-centered osteogenesis function.

  6. Microscale surface modifications for heat transfer enhancement.

    Science.gov (United States)

    Bostanci, Huseyin; Singh, Virendra; Kizito, John P; Rini, Daniel P; Seal, Sudipta; Chow, Louis C

    2013-10-09

    In this experimental study, two surface modification techniques were investigated for their effect on heat transfer enhancement. One of the methods employed the particle (grit) blasting to create microscale indentations, while the other used plasma spray coating to create microscale protrusions on Al 6061 (aluminum alloy 6061) samples. The test surfaces were characterized using scanning electron microscopy (SEM) and confocal scanning laser microscopy. Because of the surface modifications, the actual surface area was increased up to 2.8× compared to the projected base area, and the arithmetic mean roughness value (Ra) was determined to vary from 0.3 μm for the reference smooth surface to 19.5 μm for the modified surfaces. Selected samples with modified surfaces along with the reference smooth surface were then evaluated for their heat transfer performance in spray cooling tests. The cooling system had vapor-atomizing nozzles and used anhydrous ammonia as the coolant in order to achieve heat fluxes up to 500 W/cm(2) representing a thermal management setting for high power systems. Experimental results showed that the microscale surface modifications enhanced heat transfer coefficients up to 76% at 500 W/cm(2) compared to the smooth surface and demonstrated the benefits of these practical surface modification techniques to enhance two-phase heat transfer process.

  7. Strong cation exchange chromatography in analysis of posttranslational modifications: innovations and perspectives.

    Science.gov (United States)

    Edelmann, Mariola J

    2011-01-01

    Strong cation exchange (SCX) chromatography has been utilized as an excellent separation technique that can be combined with reversed-phase (RP) chromatography, which is frequently used in peptide mass spectrometry. Although SCX is valuable as the second component of such two-dimensional separation methods, its application goes far beyond efficient fractionation of complex peptide mixtures. Here I describe how SCX facilitates mapping of the protein posttranslational modifications (PTMs), specifically phosphorylation and N-terminal acetylation. The SCX chromatography has been mainly used for enrichment of these two PTMs, but it might also be beneficial for high-throughput analysis of other modifications that alter the net charge of a peptide.

  8. Surface Modification of Catalytic Materials

    DEFF Research Database (Denmark)

    Nierhoff, Anders Ulrik Fregerslev

    aggregation techniques. With the use of two different filter mechanisms, the Quadrupole and the Lateral Time Of Flight, the nanoparticles were mass selected. This was done to correlate nanoparticle size with reactivity. Selected key findings can be summarized as: 1) CO induced surface changes of Pt based...

  9. Anionic and cationic Hofmeister effects on hydrophobic and hydrophilic surfaces.

    Science.gov (United States)

    Schwierz, Nadine; Horinek, Dominik; Netz, Roland R

    2013-02-26

    Using a two-step modeling approach, we address the full spectrum of direct, reversed, and altered ionic sequences as the charge of the ion, the charge of the surface, and the surface polarity are varied. From solvent-explicit molecular dynamics simulations, we extract single-ion surface interaction potentials for halide and alkali ions at hydrophilic and hydrophobic surfaces. These are used within Poisson-Boltzmann theory to calculate ion density and electrostatic potential distributions at mixed polar/unpolar surfaces for varying surface charge. The resulting interfacial tension increments agree quantitatively with experimental data and capture the Hofmeister series, especially the anomaly of lithium, which is difficult to obtain using continuum theory. Phase diagrams that feature different Hofmeister series as a function of surface charge, salt concentration, and surface polarity are constructed from the long-range force between two surfaces interacting across electrolyte solutions. Large anions such as iodide have a high hydrophobic surface affinity and increase the effective charge magnitude on negatively charged unpolar surfaces. Large cations such as cesium also have a large hydrophobic surface affinity and thereby compensate an external negative charge surface charge most efficiently, which explains the well-known asymmetry between cations and anions. On the hydrophilic surface, the size-dependence of the ion surface affinity is reversed, explaining the Hofmeister series reversal when comparing hydrophobic with hydrophilic surfaces.

  10. Solution Versus Gas-Phase Modification of Peptide Cations with NHS-Ester Reagents

    Science.gov (United States)

    Mentinova, Marija; Barefoot, Nathan Z.; McLuckey, Scott A.

    2012-02-01

    A comparison between solution and gas phase modification of primary amine sites in model peptide cations with N-hydroxysuccinimide (NHS) ester reagents is presented. In all peptides, the site of modification in solution was directed to the N-terminus by conducting reactions at pH = 5, whereas for the same peptides, a lysine residue was preferentially modified in the gas phase. The difference in pKa values of the N-terminus and ɛ-amino group of the lysine allows for a degree of control over sites of protonation of the peptides in aqueous solution. With removal of the dielectric and multiple charging of the peptide ions in the gas phase, the accommodation of excess charge can affect the preferred sites of reaction. Interaction of the lone pair of the primary nitrogen with a proton reduces its nucleophilicity and, as a result, its reactivity towards NHS-esters. While no evidence for reaction of the N-terminus with sulfo-NHS-acetate was noted in the model peptide cations, a charge inversion experiment using bis[sulfosuccinimidyl] suberate, a cross-linking reagent with two sulfo-NHS-ester functionalities, showed modification of the N-terminus. Hence, an unprotonated N-terminus can serve as a nucleophile to displace NHS, which suggests that its lack of reactivity with the peptide cations is likely due to the participation of the N-terminus in solvating excess charge.

  11. Gaseous phase coal surface modification

    Energy Technology Data Exchange (ETDEWEB)

    Okoh, J.M.; Pinion, J.; Thiensatit, S.

    1992-05-07

    In this report, we present an improved, feasible and potentially cost effective method of cleaning and beneficiating ultrafine coal. Increased mechanization of mining methods and the need towards depyritization, and demineralization have led to an increase in the quantity of coal fines generated in recent times. For example, the amount of {minus}100 mesh coal occurring in coal preparation plant feeds now typically varies from 5 to 25% of the total feed. Environmental constraints coupled with the greatly increased cost of coal have made it increasingly important to recover more of these fines. Our method chemically modifies the surface of such coals by a series of gaseous phase treatments employing Friedel-Crafts reactions. By using olefins (ethene, propene and butene) and hydrogen chloride catalyst at elevated temperature, the surface hydrophobicity of coal is enhanced. This increased hydrophobicity is manifest in surface phenomena which reflect conditions at the solid/liquid interphase (zeta potential) and those which reflect conditions at the solid/liquid/gas interphases (contact angle, wettability and floatability).

  12. Selective Surface Modification on Lubricant Retention

    Science.gov (United States)

    Jiang, Yu; Suvanto, Mika; Pakkanen, Tapani A.

    2016-11-01

    While surface patterns are effective in improving tribological properties, nevertheless they alter the surface wettability, which will in turn affect the surface-lubricant interactions. When there is a shortage of lubricant on a patterned surface, the lubricant stored inside the cavities will be extracted to compensate the surface lubricant dissipation. Additionally, the lubricant retention effect provided by the cavities is competing with the release of the lubricant. With weak surface-lubricant interaction, the retention is limited. Therefore, the lubrication will have a sudden failure, giving a dramatic transition to abrasive wear. To improve the performance of polar lubricants on hydrophobic polymer surfaces, both topographical and selective surface modifications were incorporated on injection molded polypropylene surfaces. Distinctive lubrication improvement was observed when the surface structure density for the lubricant storage was high, and the release of the lubricant was controlled by the interaction with the selectively modified surfaces.

  13. Surface Modification of Nanocellulose Substrates

    Science.gov (United States)

    Zoppe, Justin Orazio

    Cellulose fibers constitute an important renewable raw material that is utilized in many commercial applications in non-food, paper, textiles and composite materials. Chemical functionalization is an important approach for improving the properties of cellulose based materials. Different approaches are used to graft polymeric chains onto cellulose substrates, which can be classified by two principal routes, namely 'grafting onto' or 'grafting from' methods. Never-dried cellulose nanocrystals (CNCs) or nanowhiskers produced from sulfuric acid hydrolysis of ramie fibers were used as substrates for surface chemical functionalization with various macromolecules. In addition, the use of cellulose nanocrystals to reinforce poly(epsilon-caprolactone) (PCL) nanofibers was studied. Chemical grafting with low molecular weight polycaprolactone diol onto cellulose nanocrystals was carried out in an attempt to improve the interfacial adhesion with the fiber matrix. Significant improvements in the mechanical properties of the nanofibers after reinforcement with unmodified cellulose nanocrystals were confirmed. Fiber webs from PCL reinforced with 2.5% unmodified CNCs showed ca. 1.5-fold increase in Young's modulus and ultimate strength compared to PCL webs. The CNCs were also grafted with poly(N-isopropylacrylamide) (poly(NiPAAm)) brushes via surface-initiated single-electron transfer living radical polymerization (SI-SETLRP) under various conditions at room temperature. The grafting process depended on the initiator and/or monomer concentrations used. No observable damage occurred to the CNCs after grafting, as determined by X-ray diffraction. Size exclusion chromatography analyses of polymer chains cleaved from the cellulose nanocrystals indicated that a higher degree of polymerization was achieved by increasing initiator or monomer loading, most likely caused by local heterogeneities yielding higher rates of polymerization. In addition, the colloidal stability and thermo

  14. Surface property modification of silicon

    Science.gov (United States)

    Danyluk, S.

    1984-01-01

    The main emphasis of this work has been to determine the wear rate of silicon in fluid environments and the parameters that influence wear. Three tests were carried out on single crystal Czochralski silicon wafers: circular and linear multiple-scratch tests in fluids by a pyramidal diamond simulated fixed-particle abrasion; microhardness and three-point bend tests were used to determine the hardness and fracture toughness of abraded silicon and the extent of damage induced by abrasion. The wear rate of (100) and (111) n and p-type single crystal Cz silicon abraded by a pyramidal diamond in ethanol, methanol, acetone and de-ionized water was determined by measuring the cross-sectional areas of grooves of the circular and linear multiple-scratch tests. The wear rate depends on the loads on the diamond and is highest for ethanol and lowest for de-ionized water. The surface morphology of the grooves showed lateral and median cracks as well as a plastically deformed region. The hardness and fracture toughness are critical parameters that influence the wear rate. Microhardness tests were conducted to determine the hardness as influenced by fluids. Median cracks and the damage zone surrounding the indentations were also related to the fluid properties.

  15. Surface Modifications of Organic Fillers to Improve the Strength of Paperboard

    Directory of Open Access Journals (Sweden)

    Sun Young Kim

    2015-01-01

    Full Text Available In a previous study the authors determined that non-woody materials including brewers’ grain (BG and oil palm frond (OPF could be alternatives to wood powder as organic fillers. However, they have the disadvantage of deteriorating the strength of paperboard. If the strength of paperboard could be improved, then one would expect more production cost reductions and bulk improvements by increasing the addition of organic fillers. In this study, surface modification of organic fillers was used as a method to improve paperboard strength. The goal was to find the most effective condition for surface modifications. Surface modifications of BG and OPF fillers were carried out using cationic and oxidized starches, and the strengths and reductions in the drying energies of the sheets were measured. The zeta potentials of the modified organic fillers showed that the surface modifications were performed properly. Surface modification with starches improved the bulk and strength of the sheets simultaneously, and modification with the addition of a large amount of cationic starch was more effective in improving the strengths and the reductions in drying energies of the sheets than using cationic and oxidized starches together.

  16. Surface hopping investigation of the relaxation dynamics in radical cations

    Energy Technology Data Exchange (ETDEWEB)

    Assmann, Mariana; Matsika, Spiridoula, E-mail: smatsika@temple.edu [Department of Chemistry, Temple University, Philadelphia, Pennsylvania 19122 (United States); Weinacht, Thomas [Department of Physics, Stony Brook University, Stony Brook, New York 11794 (United States)

    2016-01-21

    Ionization processes can lead to the formation of radical cations with population in several ionic states. In this study, we examine the dynamics of three radical cations starting from an excited ionic state using trajectory surface hopping dynamics in combination with multiconfigurational electronic structure methods. The efficiency of relaxation to the ground state is examined in an effort to understand better whether fragmentation of cations is likely to occur directly on excited states or after relaxation to the ground state. The results on cyclohexadiene, hexatriene, and uracil indicate that relaxation to the ground ionic state is very fast in these systems, while fragmentation before relaxation is rare. Ultrafast relaxation is facilitated by the close proximity of electronic states and the presence of two- and three-state conical intersections. Examining the properties of the systems in the Franck-Condon region can give some insight into the subsequent dynamics.

  17. Mechanism of Surface Modification for Sericite

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Surface modification of sericite by wet method was conducted with the addition of 1.0% (w/w) silane. The resulting wetting contact angle and activity ratio of sericite were 130° and 98% respectively.Good pre-evaluation indexes of oil value (40.8%) and dispersivity (14.0 mL) were obtained. When 30% of sericite was filled into acrylonitrile butadiene styrene(ABS) plastic, the bending strength and tensile strength of the composite material were reduced by 7% and 14.3% in comparison to those of pure ABS plastic, while the rigidity was increased by 3 times, and the impact strength and breaking elongation were reduced significantly.The mechanism of surface modification was investigated and the configuration of silane coupling agent on the surface of sericite was given. Infrared (IR) spectroscopic analysis indicates that the adsorption of silane on the surface of sericite belongs to chemical adsorption.

  18. Carbon Surface Modification for Enhanced Corrosion Resistance

    Science.gov (United States)

    2008-01-01

    2 R. Rayne,1 and R.A. Bayles1 1Chemistry Division 2SAIC Introduction: Case hardening by carburization has long been recognized to produce wear... carburization technique has been developed for intro- ducing carbon into stainless steel surfaces without formation of carbides.1,2 This surface modification...Michal, F. Ernst, H. Kahn, Y. Cao, F. Oba, N. Agarwal, and A.H. Heuer, “Carbon Supersaturation due to Paraequilibrium Carburization : Stainless

  19. Inorganic Surface Modification of Nonwoven Polymeric Substrates

    Science.gov (United States)

    Halbur, Jonathan Chandler

    In this study, atomic layer deposition (ALD), a vapor phase inorganic thin film deposition technique, is used to modify the surface of a range of industrially relevant polymers to enhance surface properties or impart additional functionalities. Several unique demonstrations of polymer surface modification are presented including uniform nanomaterial photodeposition to the surface of nonowoven fabrics and the first application of photocatalytic thin film coated nonwovens for advanced filtration of heavy metals from solution. Recent advances in polymer synthesis and processing technologies have resulted in the production of novel polymer systems with unique chemistries and sub-micron scale dimensions. As a result, advanced fiber systems have received much attention for potential use in a wide range of industrially and medically important applications such as advanced and selective filtration, catalysis, flexible electronics, and tissue engineering. However, tailoring the surface properties of the polymer is still needed in order to realize the full range of advanced applications, which can be difficult given the high complexity and non-uniformity of nonwoven polymeric structures. Uniform and controllable inorganic surface modification of nonwovens allows the introduction or modification of many crucial polymer properties with a wide range of application methods.

  20. Graphite Surface Modification by Heterogeneous Nucleation Process

    Institute of Scientific and Technical Information of China (English)

    CAO Ran; LI Hongxia

    2006-01-01

    Flaky graphite particles were coated by ZrOCl2·8H2O as precursors by heterogeneous nucleation process.The effects of factors such as pH values (2.4-5.1),concentration of the precursor solution (0.005-0.1 mol·L-1 ) , mixing method of graphite and precursor solution on the surface modification of graphite were studied. Result shows that: 1) the preferable technical process for heterogeneous nucleation modified graphite is to mix the graphite suspension and precursor solution with concentration 0. 025 mol·L -1 and then drip ammonia water to adjust the pH value to 3.6; 2)By surface modification, the ZrO2 particles are evenly coated on graphite surface and therefore improve oxidation resistance and dispersion ability of graphite.

  1. MODIFICATION OF TRANSITION METAL CATIONS TO POLYMER- STABILIZED PLATINUM COLLOIDAL CLUSTERS IN ENANTIOSELECTIVE HYDROGENATION OF METHYL PYRUVATE

    Institute of Scientific and Technical Information of China (English)

    Xiao-ping Yan; Bao-lin He; Jie Zhang; Han-fan Liu

    2005-01-01

    Modification of transition metal cations to polymer-stabilized Pt colloidal clusters modified with cinchonidine was studied in enantioselective hydrogenation of methyl pyruvate. Compared to the enantiomeric excess (e.e.) value (71.4%)obtained without the presence of metal cations, obvious e.e. enhancement (up to 82.5%) was resulted from the addition of Zn2+ but with a certain decrease in activity. The reaction parameters in the presence of Zn2+ were also studied. It was found that the Pt colloidal catalysts in the presence of metal cations performed very differently from that in the absence of metal cations.

  2. Surface modification and functionalization of nanostructured carbons

    Directory of Open Access Journals (Sweden)

    A. Stanishevsky

    2009-12-01

    Full Text Available Purpose: Nanostructured carbon nanomaterials (e.g., nanocrystalline diamond films and particles, carbon nanotubes, carbon onions, fullerenes, etc. are being extensively explored for numerous biomedical applications in surgical implants, therapy, drug delivery, and biosensoring due to their interesting physical, chemical, and biological properties. Such applications of carbon nanomaterials often require specific surface functionality to be introduced for better integration of these materials with physiological environment. In the last decade, substantial progress has been made in the development of controllable surface modification methods and in the introduction of different functional groups on the surface of carbon nanomaterials.Design/methodology/approach: This paper briefly overviews the surface modification and functionalization approaches for various carbon nanomaterials, and it focuses on the plasma modification and functionalization of nanocrystalline diamond films, diamond nanoparticles, and carbon nanospheres. The results on the surface characterization using FTIR and XPS techniques, and the preliminary studies of cellular response to these modified carbon nanomaterials are presented and discussed.Findings: The results of surface modification of NCD films, detonation nanodiamonds, and carbon nanospheres, demonstrate the flexibility of nanocarbons to attain various surface functionality that can be adjusted for specific applications. It has been shown that neither of tested nanocarbon materials was cytotoxic in this study, although the attachement and proliferation of various cells was strongly affected by the specific type of surface functionalization.Research limitations/implications: At the present, it is not clear to what degree the available surface sites on NCD films or carbon nanoparticles can be occupied with functional groups. Furthermore, while there is clear selectivity of cellular response to H, O, and F surface

  3. Strong Cation Exchange Chromatography in Analysis of Posttranslational Modifications: Innovations and Perspectives

    Directory of Open Access Journals (Sweden)

    Mariola J. Edelmann

    2011-01-01

    Full Text Available Strong cation exchange (SCX chromatography has been utilized as an excellent separation technique that can be combined with reversed-phase (RP chromatography, which is frequently used in peptide mass spectrometry. Although SCX is valuable as the second component of such two-dimensional separation methods, its application goes far beyond efficient fractionation of complex peptide mixtures. Here I describe how SCX facilitates mapping of the protein posttranslational modifications (PTMs, specifically phosphorylation and N-terminal acetylation. The SCX chromatography has been mainly used for enrichment of these two PTMs, but it might also be beneficial for high-throughput analysis of other modifications that alter the net charge of a peptide.

  4. Surface modification: advantages, techniques, and applications

    Energy Technology Data Exchange (ETDEWEB)

    Natesan, K.

    2000-03-01

    Adequate performance of materials at elevated temperatures is a potential problem in many systems within the chemical, petroleum, process, and power-generating industries. Degradation of materials occurs because of interaction between the structural material and the exposure environment. These interactions are generally undesired chemical reactions that can lead to accelerated wastage and alter the functional requirements and/or structural integrity of the materials. Therefore, material selection for high-temperature applications must be based not only on a material strength properties but also on resistance to the complex environments prevalent in the anticipated exposure environment. As plants become larger, the satisfactory performance and reliability of components play a greater role in plant availability and economics. However, system designers are becoming increasingly concerned with finding the least expensive material that will satisfactorily perform the design function for the desired service life. This present paper addresses the benefits of surface modification and identified several criteria for selection and application of modified surfaces in the power sector. A brief review is presented on potential methods for modification of surfaces, with the emphasis on coatings. In the final section of the paper, several examples address the requirements of different energy systems and surface modification avenues that have been applied to resolve the issues.

  5. Effects of hydrochloric acid modification on the channel characteristics, composition, surface potential and cation exchange behavior of natural clinoptilolite%盐酸改性对天然斜发沸石孔道特征、成分、表面电位及阳离子交换性能的影响

    Institute of Scientific and Technical Information of China (English)

    霍汉鑫; 林海; 董颖博; 刘泉利; 曹丽霞; 程皝; 汪涵; 傅川

    2015-01-01

    采用不同浓度盐酸对天然斜发沸石进行改性,并系统地研究了改性沸石的孔道特征、化学成分、表面电位及阳离子交换性能的变化.盐酸改性后,沸石晶体结构破坏较小,表面变得疏松粗糙,K+、Na+、Ca2+和Mg2+元素含量均小幅下降;表面负电荷增加,阳离子交换容量减小;比表面积和总孔体积均有所提高,最高分别从原沸石的35.97 m2·g -1和0.0761 m3·g-1提高至64.46 m2·g-1和0.1156 m3·g-1.盐酸改性对沸石微孔、介孔和大孔的分布影响明显.从迟滞回线形状判断沸石孔道类型均为不均匀狭缝型孔道,盐酸改性不会改变沸石孔道类型.%ABSTRACT Natural clinoptilolite was modified by different concentrations of hydrochloric acid. Systemic investigations were performed on the channel characteristics, chemical composition, surface potential, and cation exchange behavior of the modified clinoptilolite. It is found that the surface of the modified clinoptilolite becomes loose and rough, the contents of K+, Na+, Ca2+, and Mg2+ slightly decrease, the surface negative charges increases, and the cation exchange capacity decreases to some extent. The specif-ic surface area and total pore volume are improved and the maximum values of them increase from 35.97 m2·g-1 and 0.0761 m3·g-1 to 64.46 m2·g-1 and 0.1156 m3·g-1 , respectively. The distribution of micropores, mesopores, and macropores is obviously impacted, and the type of zeolite cavities is determined to be uneven slits by the hysteresis loop shape, indicating that this acid modification cannot change zeolite cavities.

  6. Synthesis of Branch Fluorinated Cationic Surfactant and Surface Properties

    Directory of Open Access Journals (Sweden)

    Hongke Wu

    2014-01-01

    Full Text Available A novel fluorinated quaternary ammonium salt cationic surfactant N,N,N-trimethyl-2-[[4-[[3,4,4,4-tetrafluoro-2-[1,2,2,2-tetrafluoro-1-(trifluoromethylethyl]-1,3-bis(tri-fluoromethyl-1-buten-1-yl]oxy]-benzoyl]amino]-iodide (FQAS was synthesized successfully, and its structure was characterized by FTIR, 1H-NMR, 19F-NMR, and MS. The surface activities of FQAS and the effect of temperature, electrolyte, and combination with hydrocarbon surfactant were investigated. The results showed that FQAS exhibited excellent surface activity and combination with hydrocarbon surfactant.

  7. Surface modification of barite nanoparticles using stearate

    Institute of Scientific and Technical Information of China (English)

    LI Lin-lin; HANG Jian-zhong; SHI Li-yi

    2009-01-01

    In this study,the barite nanoparticles were successfully modified with stearate and the influence of stearate addition on the performance of barite nanoparticles was systematically investigated.The products were characterized by activating factor analysis,contact angle test,surface energy calculation,sedimentation rate calculation,rheological measurement,and FT-IR analysis,etc.As the quantity of added stearate increased,both the activating factor and contact angle of barite nanoparticles increased first then decreased.When the stearate content was 5% of the mass of barite nanoparticles,the activating factor and water contact angle of modified particles reached maximum value,97% and 126~ respectively.At this time,the sedimentation rate reached minimum,and so did the surface energy.The rheological test reveals that the viscosity of modified barite nanoparticles/ petronol system decreases greatly,indicating the surface performance of barite nanoparticles has changed from hydrophilicity to lipophilicity after modification.C=O and COO stretching vibration peaks were found in the FT-IR spectra,which proves that the stearate has combined onto the surface of barite nanoparticles.Finally,according to the zeta potential result of unmodified barite,the possible modification mechanism was provided.

  8. Non-Surface Activity of Cationic Amphiphilic Diblock Copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Nayak, Rati Ranjan; Yamada, Tasuku; Matsuoka, Hideki, E-mail: ratiranjan@immt.res.in, E-mail: matsuoka@star.polym.kyoto-u.ac.jp [Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Nishikyo-ku, Kyoto 615-8510 (Japan)

    2011-09-19

    Cationic amphiphilic diblock copolymers containing quaternized poly (2-vinylpyridine) chain as a hydrophilic segment (PIp-b-PNMe2VP) were synthesized by living anionic polymerization. By IR measurement, we confirmed the quaternization of the polymer (PIp-b-PNMe2VP), and determined the degree of quaternization by conductometric titration. The surface tension experiment showed that the polymers are non-surface active in nature. The foam formation of the polymer solutions was also investigated with or without added salt. Almost no foam formation behavior was observed without added salt, while a little foam was observed in the presence of 1M NaCl. The critical micelle concentration (cmc) of the diblock copolymers with 3 different chain lengths was measured by the static light scattering method. The cmc values obtained in this study were much lower than the values obtained for anionic non-surface active diblock polymers studied previously. The hydrodynamic radii of the polymer micelle increased slightly in the presence of 1 M NaCl. The transmission electron microscopic images revealed spherical micelles in pure water. In the presence of salt, the cmc values increased as was the case for anionic polymers, which is unlike conventional surfactant systems but consistent with non-surface active anionic block copolymers. The microviscosity of the micelle core was evaluated using Coumarin-153 as a fluorescent anisotropy probe using steady-sate fluorescence depolarization. Non-surface activity has been proved to be universal for ionic amphiphilic block copolymers both for anionic and cationic. Hence, the origin of non-surface activity is not the charged state of water surface itself, but should be an image charge repulsion at the air/water interface.

  9. Electric Field Induced Surface Modification of Au

    Energy Technology Data Exchange (ETDEWEB)

    Erchak, A.A.; Franklin, G.F.; Houston, J.E.; Mayer, T.M.; Michalske, T.A.

    1999-02-15

    We discuss the role of localized high electric fields in the modification of Au surfaces with a W probe using the Interfacial Force Microscope. Upon bringing a probe close to a Au surface, we measure both the interfacial force and the field emission current as a function of separation with a constant potential of 100 V between tip and sample. The current initially increases exponentially as the separation decreases. However, at a distance of less than {approximately} 500{angstrom} the current rises sharply as the surface begins to distort and rapidly close the gap. Retraction of the tip before contact is made reveals the formation of a mound on the surface. We propose a simple model, in which the localized high electric field under the tip assists the production of mobile Au adatoms by detachment from surface steps, and a radial field gradient causes a net flux of atoms toward the tip by surface diffusion. These processes give rise to an unstable surface deformation which, if left unchecked, results in a destructive mechanical contact. We discuss our findings with respect to earlier work using voltage pulses in the STM as a means of nanofabrication.

  10. Surface modification of polypropylene based particle foams

    Science.gov (United States)

    Schreier, P.; Trassl, C.; Altstädt, V.

    2014-05-01

    This paper deals with the modification of the surface properties of expanded polypropylene (EPP). EPP is a semi-hard to soft elastic thermoplastic foam. The characteristic surface of EPP shows process-related steam nozzle imprints and gussets. Therefore EPP does not satisfy the quality requirements for visible automotive applications. In order to meet these demands, plastic surfaces are usually enhanced with functional or decorative coatings, e.g. textiles, plastic films or paint. The coating of plastics with low surface energies such as PP often leads to adhesion problems by reason of the missing polar and functional groups. This paper gives an evaluation of activation and pre-treatment methods of EPP, with the aim to identify the most suitable pre-treatment method. For this purpose five typical surface treatment methods - flame treatment, corona, fluorination, atmospheric and low-pressure plasma - were performed on EPP samples. As a comparison criterion the maximum increase in the adhesion force between a polyurethane-based coating and the modified EPP substrate was selected. Moreover the influence of the selected pre-treatment method on the increase in the total surface energy and its polar component was investigated by the drop shape analysis method. The results showed that the contact angle measurement is a suitable method to determine the polar and disperse fractions of the surface tension of EPP. Furthermore, all performed methods increased the adhesion of EPP.

  11. Atmospheric pressure plasma for surface modification

    CERN Document Server

    Wolf, Rory A

    2012-01-01

    This Book's focus and intent is to impart an understanding of the practical application of atmospheric plasma for the advancement of a wide range of current and emerging technologies. The primary key feature of this book is the introduction of over thirteen years of practical experimental evidence of successful surface modifications by atmospheric plasma methods. It offers a handbook-based approach for leveraging and optimizing atmospheric plasma technologies which are currently in commercial use. It also offers a complete treatment of both basic plasma physics and industrial plasma process

  12. Femtosecond laser-induced surface wettability modification of polystyrene surface

    Science.gov (United States)

    Wang, Bing; Wang, XinCai; Zheng, HongYu; Lam, YeeCheong

    2016-12-01

    In this paper, we demonstrated a simple method to create either a hydrophilic or hydrophobic surface. With femtosecond laser irradiation at different laser parameters, the water contact angle (WCA) on polystyrene's surface can be modified to either 12.7° or 156.2° from its original WCA of 88.2°. With properly spaced micro-pits created, the surface became hydrophilic probably due to the spread of the water droplets into the micro-pits. While with properly spaced micro-grooves created, the surface became rough and more hydrophobic. We investigated the effect of laser parameters on WCAs and analyzed the laser-treated surface roughness, profiles and chemical bonds by surface profilometer, scanning electron microscope (SEM) and X-ray photoelectron spectroscopy (XPS). For the laser-treated surface with low roughness, the polar (such as C—O, C=O, and O—C=O bonds) and non-polar (such as C—C or C—H bonds) groups were found to be responsible for the wettability changes. While for a rough surface, the surface roughness or the surface topography structure played a more significant role in the changes of the surface WCA. The mechanisms involved in the laser surface wettability modification process were discussed.

  13. Surface modification of nano-apatite by grafting organic polymer

    NARCIS (Netherlands)

    Liu, Qing; Wijn, de Joost R.; Groot, de Klaas; Blitterswijk, van Clemens A.

    1998-01-01

    Since surface properties of hydroxyapatite (HA) play an important role in its performance, surface modification of HA has gained much attention from researchers. Silane coupling agents have been the focus of the research. In this study, an effective surface modification method was developed using he

  14. Covalent modification of a ten-residue cationic antimicrobial peptide with levofloxacin

    Directory of Open Access Journals (Sweden)

    Carlos Alberto Rodriguez

    2014-09-01

    Full Text Available The rampant spread of antibiotic resistant bacteria has spurred interest in alternative strategies for developing next-generation antibacterial therapies. As such, there has been growing interest in cationic antimicrobial peptides (CAMPs and their therapeutic applications. Modification of CAMPs via conjugation to auxiliary compounds, including small molecule drugs, is a new approach to developing effective, broad-spectrum antibacterial agents with novel physicochemical properties and versatile antibacterial mechanisms. Here, we’ve explored design parameters for engineering CAMPs conjugated to small molecules with favorable physicochemical and antibacterial properties by covalently affixing a fluoroquinolone antibiotic, levofloxacin, to the ten-residue CAMP Pep-4. Relative to the unmodified Pep-4, the conjugate was found to demonstrate substantially increased antibacterial potency under high salt concentrations. Historically, it has been observed that most CAMPs lose antibacterial effectiveness in such high ionic strength environments, a fact that has presented a challenge to their development as therapeutics. Physicochemical studies revealed that P4LC was more hydrophobic than Pep-4, while mechanistic findings indicated that the conjugate was more effective at disrupting bacterial membrane integrity. Although the inherent antibacterial effect of the incorporated levofloxacin molecules did not appear to be substantially realized in this conjugate, these findings nevertheless suggest that covalent attachment of small molecule antibiotics with favorable physicochemical properties to CAMPs could be a promising strategy for enhancing peptide performance and overall therapeutic potential. These results have broader applicability to the development of future CAMP-antibiotic conjugates for potential therapeutic applications.

  15. Surface modification of polyester biomaterials for tissue engineering.

    Science.gov (United States)

    Jiao, Yan-Peng; Cui, Fu-Zhai

    2007-12-01

    Surfaces play an important role in a biological system for most biological reactions occurring at surfaces and interfaces. The development of biomaterials for tissue engineering is to create perfect surfaces which can provoke specific cellular responses and direct new tissue regeneration. The improvement in biocompatibility of biomaterials for tissue engineering by directed surface modification is an important contribution to biomaterials development. Among many biomaterials used for tissue engineering, polyesters have been well documented for their excellent biodegradability, biocompatibility and nontoxicity. However, poor hydrophilicity and the lack of natural recognition sites on the surface of polyesters have greatly limited their further application in the tissue engineering field. Therefore, how to introduce functional groups or molecules to polyester surfaces, which ideally adjust cell/tissue biological functions, becomes more and more important. In this review, recent advances in polyester surface modification and their applications are reviewed. The development of new technologies or methods used to modify polyester surfaces for developing their biocompatibility is introduced. The results of polyester surface modifications by surface morphological modification, surface chemical group/charge modification, surface biomacromolecule modification and so on are reported in detail. Modified surface properties of polyesters directly related to in vitro/vivo biological performances are presented as well, such as protein adsorption, cell attachment and growth and tissue response. Lastly, the prospect of polyester surface modification is discussed, especially the current conception of biomimetic and molecular recognition.

  16. Modification of the functionality of soil biogeochemical interfaces: Impact of sorbed cation and temperature

    Science.gov (United States)

    Bachmann, Joerg; Woche, Susanne K.

    2010-05-01

    Soil as a porous 3-phase system is characterized by a tremendously high surface area to volume ratio. Complex interactions of physical, chemical and biological processes occur at biogeochemical interfaces generally formed in living media like soil. Along with electrostatic interactions, the interfacial properties (surface free energies) control wetting kinetics, physical status of adsorbed water films, flocculation, adsorption, and they are also a major contributor to the rheological properties of dispersions. To describe the surface properties in a mechanistic way it is crucial to understand complex biological, physical and hydraulical processes within a general mechanistic framework. Biogeochemical interfaces, on one hand, signicantly determine the relationship between the surface geochemistry of a pore domain and the micoorganism or plant life in that specific region. On the other hand, they determine additionally with the pore geometry (local pore diameter, turtuosity and connectivity) the hydraulic properties of the pore domain. However, until now no physically measurable surface property has been established to determine all aspects mentioned above with one set of parameters. One of the key physicochemical parameters for describing the interaction of water and colloids is the interfacial free energy which is basically measured through contact angle measurements. With respect to water repellency we will present approaches and problems related to the evaluation of soil wettability for a sandy topsoil and a peat soil. Hence, the first part of the study emphasizes a framework to determine the mixed hydrophilic-hydrophobic behavior of particle surfaces. Furthermore, the sensitivity of physical impact of frequently changing conditions in soil like cation composition of soil solution and temperature is analyzed. We conclude that the wettability of OM, quantified by the contact angle, links specifically the chemical structure of SOM with a bundle of physical soil

  17. A general strategy for the ultrafast surface modification of metals

    OpenAIRE

    Shen, Mingli; Zhu, Shenglong; Wang, Fuhui

    2016-01-01

    Surface modification is an essential step in engineering materials that can withstand the increasingly aggressive environments encountered in various modern energy-conversion systems and chemical processing industries. However, most traditional technologies exhibit disadvantages such as slow diffusion kinetics, processing difficulties or compatibility issues. Here, we present a general strategy for the ultrafast surface modification of metals inspired by electromigration, using aluminizing au...

  18. Theoretical Investigation on the Adsorption of Ag+ and Hydrated Ag+ Cations on Clean Si(111)Surface

    Institute of Scientific and Technical Information of China (English)

    SHENG Yong-Li; LI Meng-Hua; WANG Zhi-Guo; LIU Yong-Jun

    2008-01-01

    In this paper,the adsorption of Ag+ and hydrated Ag+ cations on clean Si(111)surface were investigated by using cluster(Gaussian 03)and periodic(DMol3)ab initio calculations.Si(111)surface was described with cluster models(Si14H17 and Si22H21)and a four-silicon layer slab with periodic boundary conditions.The effect of basis set superposition error(BSSE)was taken into account by applying the counterpoise correction.The calculated results indicated that the binding energies between hydrated Ag+ cations and clean Si(111)surface are large,suggesting a strong interaction between hydrated Ag+ cations and the semiconductor surface.With the increase of number,water molecules form hydrogen bond network with one another and only one water molecule binds directly to the Ag+ cation.The Ag+ cation in aqueous solution will safely attach to the clean Si(111)surface.

  19. Cationic starches on cellulose surfaces. A study of polyelectrolyte adsorption.

    OpenAIRE

    Steeg, van der, P.A.H.

    1992-01-01

    Cationic starches are used on a large scale in paper industry as wet-end additives. They improve dry strength. retention of fines and fillers, and drainage. Closure of the white water systems in the paper mills hase increased the concentration of detrimental substances. This might be the reason for the poor retention of cationic starches observed in the last few years.The purpose of the research described in this thesis was to obtain a better understanding of the adsorption of cationic starch...

  20. Reduction of Glass Surface Reflectance by Ion Beam Surface Modification

    Energy Technology Data Exchange (ETDEWEB)

    Mark Spitzer

    2011-03-11

    This is the final report for DOE contract DE-EE0000590. The purpose of this work was to determine the feasibility of the reduction of the reflection from the front of solar photovoltaic modules. Reflection accounts for a power loss of approximately 4%. A solar module having an area of one square meter with an energy conversion efficiency of 18% generates approximately 180 watts. If reflection loss can be eliminated, the power output can be increased to 187 watts. Since conventional thin-film anti-reflection coatings do not have sufficient environmental stability, we investigated the feasibility of ion beam modification of the glass surface to obtain reduction of reflectance. Our findings are generally applicable to all solar modules that use glass encapsulation, as well as commercial float glass used in windows and other applications. Ion implantation of argon, fluorine, and xenon into commercial low-iron soda lime float glass, standard float glass, and borosilicate glass was studied by implantation, annealing, and measurement of reflectance. The three ions all affected reflectance. The most significant change was obtained by argon implantation into both low-iron and standard soda-lime glass. In this way samples were formed with reflectance lower than can be obtained with a single-layer coatings of magnesium fluoride. Integrated reflectance was reduced from 4% to 1% in low-iron soda lime glass typical of the glass used in solar modules. The reduction of reflectance of borosilicate glass was not as large; however borosilicate glass is not typically used in flat plate solar modules. Unlike conventional semiconductor ion implantation doping, glass reflectance reduction was found to be tolerant to large variations in implant dose, meaning that the process does not require high dopant uniformity. Additionally, glass implantation does not require mass analysis. Simple, high current ion implantation equipment can be developed for this process; however, before the process

  1. Surface modifications of electrode materials for lithium ion batteries

    Science.gov (United States)

    Fu, L. J.; Liu, H.; Li, C.; Wu, Y. P.; Rahm, E.; Holze, R.; Wu, H. Q.

    2006-02-01

    electrolyte solution, suppress the phase transitions, improve the structural stability, and decrease the disorder of cations in the crystal sites. As a result, side reactions and the amount of the heat production during cycling are decreased. Simultaneously, other effects are observed such as: (1) suppression of the dissolution of Mn 2+, (2) higher conductivity, and (3) removal of HF from the electrolyte solution. Consequently, after the above-mentioned effective coating, marked improvements in the electrochemical performance of the electrode materials including the reversible capacity, the coulombic efficiency in the first cycle, the cycling behavior, and the high rate capability have been achieved. However, many surface science issues are still remaining open, e.g., mechanisms of these coatings and different actions of different coatings, and some further directions are suggested for the surface modification of the electrode materials.

  2. Chemical Modification Methods of Nanoparticles of Silicon Carbide Surface

    Directory of Open Access Journals (Sweden)

    Anton S. Yegorov

    2015-09-01

    Full Text Available silicon carbide exhibits exceptional properties: high durability, high thermal conductivity, good heat resistance, low thermal expansion factor and chemical inactivity. Reinforcement with silicon carbide nanoparticles increases polymer’s tensile strength and thermal stability.Chemical methods of modification of the silicon carbide surface by means of variety of reagents from ordinary molecules to macromolecular polymers are reviewed in the review.The structure of silicon carbide surface layer and the nature of modificator bonding with the surface of SiC particles are reviewed. General examples of surface modification methodologies and composite materials with the addition of modified SiC are given.

  3. Modification of potato peel waste with base hydrolysis and subsequent cationization.

    Science.gov (United States)

    Lappalainen, Katja; Kärkkäinen, Johanna; Joensuu, Päivi; Lajunen, Marja

    2015-11-01

    Potato peel waste (PW) is a starch containing biomaterial produced in large amounts by food processing industry. In this work, the treatment of PW by alkaline hydrolysis and cationization in the water phase is reported. In order to improve the cationization of starch, PW was hydrolyzed by heating with alkaline (NaOH) ethanol solution (80%) in a water bath. The impact of variable molar ratios of anhydroglucose unit (AGU):NaOH, heating temperatures and times was studied on the degradation of starch and the molecular size distribution of the product. The hydrolyzed PW was cationized subsequently in water by using glycidyltrimethylammonium chloride and catalyzed by NaOH under microwave irradiation or in an oil bath. The impact of the various reaction conditions on the cationization and degree of substitution of starch was studied. The degree of substitution of the cationized starch varied in the range of 0-0.35.

  4. The Progress on Laser Surface Modification Techniques of Titanium Alloy

    Institute of Scientific and Technical Information of China (English)

    LIANG Cheng; PAN Lin; Al Ding-fei; TAO Xi-qi; XIA Chun-huai; SONG Yan

    2004-01-01

    Titanium alloy is widely used in aviation, national defence, automobile, medicine and other fields because of their advantages in lower density, corrosion resistance, and fatigue resistance etc. As titanium alloy is higher friction coefficients, weak wear resistance, bad high temperature oxidation resistance and lower biocompatibility, its applications are restricted. Using laser surface modification techniques can significantly improve the surface properties of titanium alloy. a review is given for progress on laser surface modification techniques of titanium alloy in this paper.

  5. Surface modification of alumina nanoparticles with silane coupling agents

    Energy Technology Data Exchange (ETDEWEB)

    Prado, Luis A.S.A.; Sriyai, Montira; Ghislandi, Marcos; Schulte, Karl [Technische Universitaet Hamburg-Harburg, Hamburg (Germany). Inst. fuer Kunststoffe und Verbundwerkstoffe (M-11); Barros-Timmons, Ana [University of Aveiro (Portugal). Dept. of Chemistry. Centro de Investigacao em Materiais Ceramicos e Compositos (CICECO)

    2010-07-01

    In the present paper we describe the surface modification of alumina nanoparticles using epoxy-containing alkoxysilanes (silane coupling agents, SCA). The materials were characterized using infrared spectroscopy and solid-state nuclear magnetic resonance. Whereas, neat alumina nanoparticles could be expectedly modified with the afore mentioned SCA, as evidenced by {sup 13}C CPMAS NMR, the presence of arylsulphonates at the surface of alumina caused the ringopening polymerization of the epoxide. This polymerization reaction facilitated the surface modification of alumina by the SCA. X-ray powder diffraction and {sup 27}Al MAS NMR clearly demonstrated that in spite of the SCA polymerization, there were neither structural changes nor phase transitions in the alumina after the surface modification. The surface modification decreased the thermal stability of alumina, in comparison to pristine alumina nanoparticles. (author)

  6. Comparison of several innovative bridge cable surface modifications

    DEFF Research Database (Denmark)

    Kleissl, Kenneth; Georgakis, Christos T.

    Over the last two decades, several bridge cable manufacturers have introduced surface modifications on the high-density polyethylene (HDPE) sheathing that is installed for the protection of inner cable strands or wires. The modifications are based on research undertaken predominantly in Europe an...

  7. Cationic starches on cellulose surfaces. A study of polyelectrolyte adsorption.

    NARCIS (Netherlands)

    Steeg, van de H.G.M.

    1992-01-01

    Cationic starches are used on a large scale in paper industry as wet-end additives. They improve dry strength. retention of fines and fillers, and drainage. Closure of the white water systems in the paper mills hase increased the concentration of detrimental substances. This might be the reason for

  8. Surface modification of materials to encourage beneficial biofilm formation

    Directory of Open Access Journals (Sweden)

    Amreeta Sarjit

    2015-10-01

    Full Text Available Biofilms are communities of sessile microorganisms that grow and produce extrapolymeric substances on an abiotic or biotic surface. Although biofilms are often associated with negative impacts, the role of beneficial biofilms is wide and include applications in bioremediation, wastewater treatment and microbial fuel cells. Microbial adhesion to a surface, which is highly dependent on the physicochemical properties of the cells and surfaces, is an essential step in biofilm formation. Surface modification therefore represents an important way to modulate microbial attachment and ultimately biofilm formation by microorganisms. In this review different surface modification processes such as organosilane surface modification, plasma treatment, and chemical modification of carbon nanotubes, electro-oxidation and covalent-immobilization with neutral red and methylene blue molecules are outlined. The effectiveness of these modifications and their industrial applications are also discussed. There is inadequate literature on surface modification as a process to enhance beneficial biofilm formation. These methods need to be safe, economically viable, scalable and environmental friendly and their potential to fulfil these criteria for many applications has yet to be determined.

  9. Advances of Titanium Alloys and Its Biological Surface Modification

    Institute of Scientific and Technical Information of China (English)

    XU Ke-wei; HUANG Ping

    2004-01-01

    This paper reviews the past, present and future of surface modification of titanium alloy from the point of view of preparation of hard tissue replacement implants. The development of titanium alloy is also described.

  10. Impact of Dental Implant Surface Modifications on Osseointegration

    OpenAIRE

    Ralf Smeets; Bernd Stadlinger; Frank Schwarz; Benedicta Beck-Broichsitter; Ole Jung; Clarissa Precht; Frank Kloss; Alexander Gröbe; Max Heiland; Tobias Ebker

    2016-01-01

    Objective. The aim of this paper is to review different surface modifications of dental implants and their effect on osseointegration. Common marketed as well as experimental surface modifications are discussed. Discussion. The major challenge for contemporary dental implantologists is to provide oral rehabilitation to patients with healthy bone conditions asking for rapid loading protocols or to patients with quantitatively or qualitatively compromised bone. These charging conditions require...

  11. MICROWAVE-ASSISTED SURFACE MODIFICATION OF CALCIUM BICARBONATE

    Institute of Scientific and Technical Information of China (English)

    Jing Ye; Xiaofei Zhang

    2004-01-01

    Surface modification of calcium bicarbonate powder with isopropyl triisostearoyl titanate (TTS) by microwave-assisted heating was studied in the present work. The features of microwave treated powder show obvious superiority to those of powder samples treated by traditional surface modification method and of untreated calcium bicarbonate - in suspension turbidity, suction potential, contact angle with water, and mechanical properties of their composites with PVC resin.

  12. Modification of Cu surface with picosecond laser pulses

    NARCIS (Netherlands)

    Obona, J. Vincenc; Ocelik, V.; Rao, J. C.; Skolski, J. Z. P.; Romer, G. R. B. E.; in't Veld, A. J. Huis; de Hosson, Jeff

    2014-01-01

    High purity, mirror-polished polycrystalline Cu surface was treated with single picosecond laser pulses at fluence levels close to the single-pulse modification threshold. The induced surface topography and sub-surface changes were examined with scanning and transmission electron microscopy, respect

  13. Effect of Surface Modification on Behaviors of Cerium Oxide Nanopowders

    Institute of Scientific and Technical Information of China (English)

    Li Mei; Shi Zhenxue; Liu Zhaogang; Hu Yanhong; Wang Mitang; Li Hangquan

    2007-01-01

    Study was made on the effect of surface modification on the behaviors of cerium oxide nanopowders. A surfactant-sodium dodecyl sulfate(C12H25SO4Na) was used to modify the surface of CeO2 powder particles. The unmodified and modified CeO2 powders were characterized by using a powder comprehensive characteristic tester, laser particle size analyzer, specific surface area tester, X-ray diffraction tester, and a scanning electron microscope. The testing and analysis results showed that C12H25SO4Na surface modification might increase the flowability and dispersity, and decrease the specific surface area and agglomeration of CeO2 powders. The mechanism of the surface modification of CeO2 powder particles was also discussed.

  14. Polymer grafting modification of the surface of nano silicon dioxide

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Based on the composite modification technology of the surface of nano silicon dioxide by non-soap emulsion polymerization, it is verified that there are polymer grafted on the surface of nano silicon dioxide. The modification mechanism and the bonding status on the surface of nano silicon dioxide after modification were suggested via the results of the infrared spectrum, transmission electronic microscope photograph and X-ray photoelectron spectrum. The hydroxyl formed by hydrolyzing of silane coupling agent reacts with hydroxyl on the surface of nano silicon dioxide to form Si-O-Si bonds by losing water molecules and hence the double bonds are introduced onto the surface of nano silicon dioxide. The surface of nano silicon dioxide is grafted with polymer through free radical polymerization between the double bonds on the surface of nano silicon dioxide and styrene under the action of initiating agent. The dispersibility of nano silicon dioxide and the controllability of surface modification of nano silicon dioxide can be greatly improved by the modification process.

  15. Chemical Surface, Thermal and Electrical Characterization of Nafion Membranes Doped with IL-Cations

    Directory of Open Access Journals (Sweden)

    María del Valle Martínez de Yuso

    2014-04-01

    Full Text Available Surface and bulk changes in a Nafion membrane as a result of IL-cation doping (1-butyl-3-methylimidazolium tetrafluoroborate or BMIM+BF4 and phenyltrimethylammonium chloride or TMPA+Cl− were studied by X-ray photoelectron spectroscopy (XPS, contact angle, differential scanning calorimetry (DSC and impedance spectroscopy (IS measurements performed with dry samples after 24 h in contact with the IL-cations BMIM+ and TMPA+. IL-cations were selected due to their similar molecular weight and molar volume but different shape, which could facilitate/obstruct the cation incorporation in the Nafion membrane structure by proton/cation exchange mechanism. The surface coverage of the Nafion membrane by the IL-cations was confirmed by XPS analysis and contact angle, while the results obtained by the other two techniques (DSC and IS seem to indicate differences in thermal and electrical behaviour depending on the doping-cation, being less resistive the Nafion/BMIM+ membrane. For that reason, determination of the ion transport number was obtained for this membrane by measuring the membrane or concentration potential with the samples in contact with HCl solutions at different concentrations. The comparison of these results with those obtained for the original Nafion membrane provides information on the effect of IL-cation BMIM+ on the transport of H+ across wet Nafion/BMIM+ doped membranes.

  16. Surface modification of polymeric materials by cold atmospheric plasma jet

    Energy Technology Data Exchange (ETDEWEB)

    Kostov, K.G., E-mail: kostov@feg.unesp.br [Faculty of Engineering in Guaratinguetá–FEG, Universidade Estadual Paulista–UNESP Guaratiguetá, 12516-410, SP (Brazil); Nishime, T.M.C.; Castro, A.H.R. [Faculty of Engineering in Guaratinguetá–FEG, Universidade Estadual Paulista–UNESP Guaratiguetá, 12516-410, SP (Brazil); Toth, A. [Institute of Material and Environmental Chemistry, Hungarian Academy of Science P.O. Box 17, H-1525, Budapest (Hungary); Hein, L.R.O. [Faculty of Engineering in Guaratinguetá–FEG, Universidade Estadual Paulista–UNESP Guaratiguetá, 12516-410, SP (Brazil)

    2014-09-30

    Highlights: • We investigate polymer surface modification by atmospheric pressure plasma jet APPJ. • Jet operation conditions for uniform surface modification were determined. • The APPJ added O atoms to the polymer surface and also enhanced the roughness. • The degree of polymer surface modification by APPJ and DBD were compared. • The APPJ is more efficient in attaching O atoms and produces less polymer fragments. - Abstract: In this work we report the surface modification of different engineering polymers, such as, polyethylene terephthalate (PET), polyethylene (PE) and polypropylene (PP) by an atmospheric pressure plasma jet (APPJ). It was operated with Ar gas using 10 kV, 37 kHz, sine wave as an excitation source. The aim of this study is to determine the optimal treatment conditions and also to compare the polymer surface modification induced by plasma jet with the one obtained by another atmospheric pressure plasma source – the dielectric barrier discharge (DBD). The samples were exposed to the plasma jet effluent using a scanning procedure, which allowed achieving a uniform surface modification. The wettability assessments of all polymers reveal that the treatment leads to reduction of more than 40° in the water contact angle (WCA). Changes in surface composition and chemical bonding were analyzed by x-ray photoelectron spectroscopy (XPS) and Fourier-Transformed Infrared spectroscopy (FTIR) that both detected incorporation of oxygen-related functional groups. Surface morphology of polymer samples was investigated by Atomic Force Microscopy (AFM) and an increase of polymer roughness after the APPJ treatment was found. The plasma-treated polymers exhibited hydrophobic recovery expressed in reduction of the O-content of the surface upon rinsing with water. This process was caused by the dissolution of low molecular weight oxidized materials (LMWOMs) formed on the surface as a result of the plasma exposure.

  17. Enzymatic surface modification of Kevlar fibers

    Institute of Scientific and Technical Information of China (English)

    ZHAO; Jingchan; FAN; Guoning; GUO; Zhian; ZHANG; Yongke; W

    2005-01-01

    Horseradish peroxidase catalyzed grafting of acrylamide (AM) onto Kevlar fibers has been studied. The modified fiber has been characterized with scanning electron microscopy (SEM), elemental analysis and the grafting yield. From the SEM micrographs, the surface of the grafted Kevlar fiber is rougher than that of the untreated fiber, and the elemental analysis indicated that the nitrogen content of the treated fibers is higher than that of the untreated fiber. All the results suggested that AM must have been grafted onto the Kevlar surface through HRP-mediated radical initiated grafting reaction. The probably mechanism of HRP catalyzed grafting of AM onto Kevlar surface is proposed.

  18. Modification methods for poly(arylsulfone) membranes: A mini-review focusing on surface modification

    NARCIS (Netherlands)

    Nady, N.; Franssen, M.C.R.; Zuilhof, H.; Mohy Eldin, M.S.; Boom, R.M.; Schroën, C.G.P.H.

    2011-01-01

    Surface modification of membranes is thought to be equally important to the membrane industry as membrane material and process development; surface functionalization has already become a key technology, the major aims being performance improvement (flux and selectivity) by reduction of unwanted prot

  19. Practical applications of plasma surface modification

    Energy Technology Data Exchange (ETDEWEB)

    Smith, M.D.

    1993-12-01

    Radio frequency activated gas plasma is an environmentally conscious manufacturing process which provides surface treatments for improved product quality. Plasma processing offers significant potential for reducing the use of solvents and other wet processing chemicals now used in surface treatments such as cleaning, activation for bonding, and moisture removal. Plasma treatments are generally accomplished without creating hazardous waste streams to dispose of. Plasma process development and application is ongoing at Allied Signal Inc., Kansas City Division.

  20. Surface modification of solid state gas sensors

    Science.gov (United States)

    Morris, Ljuibov

    The phenomenon of electrical conductivity being controlled by the chemical state of a surface grafted reactive centre, resulting in a room temperature gas response, is demonstrated. The reactive centres can be chosen to be specific to a particular gas, providing a route to new types of gas detectors tailored for a particular application. Generalization of the phenomenon was verified. Surface grafting of Ti, Ru and Pt centres onto SnO2; Ti and Pt centres onto Ti02 ; and Pt centres onto BaSn0.97Sb0.03O3 resulted in a room temperature gas sensitivity specific to each system. Surface grafting of Ru centres onto SnO2 resulted in additional electronic states in the SnO2 band gap associated with surface Ru species, revealed by XPS and correlated with resistance increase of the material. An electronic interaction between grafted Ru centres and the SnO2 support was manifested in conductivity being controlled by the surface state of the Ru. Variations in the chemical state of the surface grafted Ru caused by gas chemisorption were revealed by XPS and this was correlated with conductivity change measured as gas response of the device at room temperature. The samples were characterized by EXAFS to confirm the structure of the surface Ru species, TPD, UV- visible spectroscopy, XPS and electrical measurements. DFT molecular cluster calculations were also performed to ascertain the origin of the gas response. The mechanism of the room temperature CO response of SnO2 decorated with small Pt particles was refined. In this case Pt was applied by common impregnation techniques. The conductivity was shown to be controlled by the surface state of the Pt. The CO response at room temperature was found to be specific to the presence of Pt(II) species. The mechanism was assigned to CO chemisorption onto Pt(II), resulting in charge transfer, measured as conductivity increase. The samples were characterized by XPS, TPD, SEM, mass spectrometry and electrical measurements. Comparison of the

  1. Nanoscale Surface Modification of Layered Materials

    Science.gov (United States)

    O'Shea, Aaron

    2011-11-01

    A scanning electron microscope can magnify a sample many times greater than a standard microscope, down to nanoscale dimensions. It can also be used to form patterns on the surfaces of certain materials, a technique used to create microchips. We have developed a technique that simplifies and expedites this process using an unmodified scanning electron microscope. Using this technique, we are able to alter the surface chemistry in a controlled pattern on a special class of materials called transition metal dichalcogenides. These materials have many useful applications: industrial lubricants; high strength nanocomposites; advanced solar cells; and next generation electronics. Altering the surface chemistry of these materials at the nanoscale results in unusual quantum behavior, which is useful in nanotechnology.

  2. A general strategy for the ultrafast surface modification of metals.

    Science.gov (United States)

    Shen, Mingli; Zhu, Shenglong; Wang, Fuhui

    2016-12-07

    Surface modification is an essential step in engineering materials that can withstand the increasingly aggressive environments encountered in various modern energy-conversion systems and chemical processing industries. However, most traditional technologies exhibit disadvantages such as slow diffusion kinetics, processing difficulties or compatibility issues. Here, we present a general strategy for the ultrafast surface modification of metals inspired by electromigration, using aluminizing austenitic stainless steel as an example. Our strategy facilitates the rapid formation of a favourable ductile surface layer composed of FeCrAl or β-FeAl within only 10 min compared with several hours in conventional processes. This result indicates that electromigration can be used to achieve the ultrafast surface modification of metals and can overcome the limitations of traditional technologies. This strategy could be used to aluminize ultra-supercritical steam tubing to withstand aggressive oxidizing environments.

  3. Magellan: initial analysis of venus surface modification.

    Science.gov (United States)

    Arvidson, R E; Baker, V R; Elachi, C; Saunders, R S; Wood, J A

    1991-04-12

    Initial Magellan observations reveal a planet with high dielectric constant materials exposed preferentially in elevated regions with high slopes, ejecta deposits extending up to 1000 kilometers to the west of several impact craters, windblown deposits and features in areas where there are both obstacles and a source of particulate material, and evidence for slow, steady degradation by atmosphere-surface interactions and mass movements.

  4. USE OF CATIONIC SURFACTANTS TO MODIFY SOIL SURFACES TO PROMOTE SORPTION AND RETARD MIGRATION OF HYDROPHOBIC ORGANIC COMPOUNDS

    Science.gov (United States)

    Cationic surfactants can be used to modify surfaces of soils and subsurface materials to promote adsorption of hydrophobic organic compounds (HOC). Batch and column experiments were performed to investigate this phenomenon with the cationic surfactant dodecylpyridinium (DP), a se...

  5. Modification of inorganic surface with 1-alkenes and 1-alkynes

    NARCIS (Netherlands)

    Maat, ter J.

    2012-01-01

    Surface modification is important because it allows the tuning of surface properties, thereby enabling new applications of a material. It can change physical properties such as wettability and friction, but can also introduce chemical functionalities and binding specificity. Several techniques are a

  6. Membrane surface modification via polymer grafting and interfacial polymerization

    Science.gov (United States)

    Membrane separation is an important technology for separating food ingredients and fractionating high-value substances from food processing by-products. Long-term uses of polymeric membranes in food protein processing are impeded by formation of fouled layers on the membrane surface. Surface modif...

  7. Surface modification of solid state gas sensors

    CERN Document Server

    Morris, L

    2000-01-01

    mechanism of the room temperature CO response of SnO sub 2 decorated with small Pt particles was refined. In this case Pt was applied by common impregnation techniques. The conductivity was shown to be controlled by the surface state of the Pt. The CO response at room temperature was found to be specific to the presence of Pt(ll) species. The mechanism was assigned to CO chemisorption onto Pt(ll), resulting in charge transfer, measured as conductivity increase. The samples were characterized by XPS, TPD, SEM, mass spectrometry and electrical measurements. Comparison of the results presented for Pt decorated BaSn sub 0 sub . sub 9 sub 7 Sb sub 0 sub . sub 0 sub 3 O sub 3 and BaFeO sub 3 demonstrated the phenomenon to be general providing that Pt particles act as surface traps, controlling the conductivity. The phenomenon of electrical conductivity being controlled by the chemical state of a surface grafted reactive centre, resulting in a room temperature gas response, is demonstrated. The reactive centres can ...

  8. Exchangeable cations-mediated photodegradation of polycyclic aromatic hydrocarbons (PAHs) on smectite surface under visible light

    Energy Technology Data Exchange (ETDEWEB)

    Jia, Hanzhong, E-mail: jiahz@ms.xjb.ac.cn [Laboratory of Environmental Sciences and Technology, Xinjiang Technical Institute of Physics & Chemistry, Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences, Urumqi 830011 (China); Li, Li [Laboratory of Environmental Sciences and Technology, Xinjiang Technical Institute of Physics & Chemistry, Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences, Urumqi 830011 (China); Chen, Hongxia; Zhao, Yue [Laboratory of Environmental Sciences and Technology, Xinjiang Technical Institute of Physics & Chemistry, Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences, Urumqi 830011 (China); School of Geology and Mining Engineering, Xinjiang University, Urumqi 830046 (China); Li, Xiyou [Laboratory of Environmental Sciences and Technology, Xinjiang Technical Institute of Physics & Chemistry, Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences, Urumqi 830011 (China); Wang, Chuanyi, E-mail: cywang@ms.xjb.ac.cn [Laboratory of Environmental Sciences and Technology, Xinjiang Technical Institute of Physics & Chemistry, Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences, Urumqi 830011 (China)

    2015-04-28

    Graphical abstract: Roles of exchangeable cations in PAHs photodegradation on clay surafces under visible light. - Highlights: • Photolysis rate are strongly dependent on the type of cations on clay surface. • The strength of “cation–π” interactions governs the photodegradation rate of PAHs. • Several exchangeable cations could cause a shift in the absorption spectrum of PAHs. • Exchangeable cations influence the type and amount of reactive intermediates. - Abstract: Clay minerals saturated with different exchangeable cations are expected to play various roles in photodegradation of polycyclic aromatic hydrocarbons (PAHs) via direct and/or indirect pathways on clay surfaces. In the present study, anthracene and phenanthrene were selected as molecule probes to investigate the roles of exchangeable cations on their photodegradation under visible light irradiation. For five types of cation-modified smectite clays, the photodegradation rate of anthracene and phenanthrene follows the order: Fe{sup 3+} > Al{sup 3+} > Cu{sup 2+} >> Ca{sup 2+} > K{sup +} > Na{sup +}, which is consistent with the binding energy of cation–π interactions between PAHs and exchangeable cations. The result suggests that PAHs photolysis rate depends on cation–π interactions on clay surfaces. Meanwhile, the deposition of anthracene at the Na{sup +}-smectite and K{sup +}-smectite surface favors solar light absorption, resulting in enhanced direct photodecomposition of PAHs. On the other hand, smectite clays saturated with Fe{sup 3+}, Al{sup 3+}, and Cu{sup 2+} are highly photoreactive and can act as potential catalysts giving rise to oxidative radicals such as O{sub 2}{sup −}· , which initiate the transformation of PAHs. The present work provides valuable insights into understanding the transformation and fate of PAHs in the natural soil environment and sheds light on the development of technologies for contaminated land remediation.

  9. Surface Modification Mechanism of Fine Coal by Electrochemical Methods

    Institute of Scientific and Technical Information of China (English)

    ZHU Hong; WANG Fang-hui; WANG Dian-zuo; OU Ze-shen

    2006-01-01

    In order to reveal the surface modification mechanism of fine coal by electrochemical methods, the structural changes of the coal surface before and after electrochemical modification were investigated by Fourier Transform Infrared Spectra (FTIR) and Raman Spectra. The results show that under certain electrochemical conditions, the oxygen-containing functional group in the coal structure and the oxygen content of absorption could be reduced and the floatability of coal improved. At the same time, the sulfur in the coal was reduced to the hydrophilic S2- which could be separated easily from coal. Thus electrochemical modification methods could be used to change the structure and functional group on the coal surface and to enhance the floatability of coal.

  10. Defining the Catechol-Cation Synergy for Enhanced Wet Adhesion to Mineral Surfaces.

    Science.gov (United States)

    Rapp, Michael V; Maier, Greg P; Dobbs, Howard A; Higdon, Nicholas J; Waite, J Herbert; Butler, Alison; Israelachvili, Jacob N

    2016-07-27

    Mussel foot proteins (Mfps) exhibit remarkably adaptive adhesion and bridging between polar surfaces in aqueous solution despite the strong hydration barriers at the solid-liquid interface. Recently, catechols and amines-two functionalities that account for >50 mol % of the amino acid side chains in surface-priming Mfps-were shown to cooperatively displace the interfacial hydration and mediate robust adhesion between mineral surfaces. Here we demonstrate that (1) synergy between catecholic and guanidinium side chains similarly promotes adhesion, (2) increasing the ratio of cationic amines to catechols in a molecule reduces adhesion, and (3) the catechol-cation synergy is greatest when both functionalities are present within the same molecule.

  11. Surface modification of titanium and titanium alloys by ion implantation.

    Science.gov (United States)

    Rautray, Tapash R; Narayanan, R; Kwon, Tae-Yub; Kim, Kyo-Han

    2010-05-01

    Titanium and titanium alloys are widely used in biomedical devices and components, especially as hard tissue replacements as well as in cardiac and cardiovascular applications, because of their desirable properties, such as relatively low modulus, good fatigue strength, formability, machinability, corrosion resistance, and biocompatibility. However, titanium and its alloys cannot meet all of the clinical requirements. Therefore, to improve the biological, chemical, and mechanical properties, surface modification is often performed. In view of this, the current review casts new light on surface modification of titanium and titanium alloys by ion beam implantation.

  12. A New Approach for the Modification of Paper Surface Properties Using Polyoxometalates

    Directory of Open Access Journals (Sweden)

    José L. Amaral

    2010-01-01

    Full Text Available A new approach for the chemical modification of the surface of paper based on the application of colloidal mixtures containing cationic starch and polyoxometalates on uncoated base paper is presented. Polyoxometalates with the Keggin-type structure and physical properties similar to those presented by coating pigments, namely H3PW12O40·23H2O, H4SiW12O40·24H2O, and K7PW11O39·9H2O, have been used in order to improve the quality of inkjet printing. The analysis of the different samples by FTIR-ATR spectroscopy showed the presence of the polyoxometalates (and the cationic starch on the top surface of the paper. In addition, the determination of surface energy parameters, namely the polar component (σsp and the dispersive component (σsd of the surface energy, by contact angle measurements revealed that, for the new samples, the polar component level was much higher than that of the uncoated base paper. The quality of inkjet printing, evaluated by parameters such as the gamut area and the optical density, was considerably improved by these surface treatments.

  13. Polydopamine-Assisted Surface Modification for Bone Biosubstitutes

    Science.gov (United States)

    Zhou, Xin

    2016-01-01

    Polydopamine (PDA) prepared in the form of a layer of polymerized dopamine (DA) in a weak alkaline solution has been used as a versatile biomimetic surface modifier as well as a broadly used immobilizing macromolecule. This review mainly discusses the progress of biomaterial surface modification inspired by the participation of PDA in bone tissue engineering. A comparison between PDA-assisted coating techniques and traditional surface modification applied to bone tissue engineering is first presented. Secondly, the chemical composition and the underlying formation mechanism of PDA coating layer as a unique surface modifier are interpreted and discussed. Furthermore, several typical examples are provided to evidence the importance of PDA-assisted coating techniques in the construction of bone biosubstitutes and the improvement of material biocompatibility. Nowadays, the application of PDA as a superior surface modifier in multifunctional biomaterials is drawing tremendous interests in bone tissue scaffolds to promote the osteointegration for bone regeneration. PMID:27595097

  14. The surface parameters modifications at nano scale for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Safonov, V; Zykova, A; Smolik, J; Rogovska, R; Donkov, N; Georgieva, V, E-mail: zykov@bi.com.u

    2010-11-01

    Functional coatings deposition is an effective way of surface modification with direct control of stoichiometry, impurity elements, functional groups and surface charges. Modified surface properties such as composition, roughness, wettability have effect on the most important processes at biomaterial interface. The aim of present study was the analysis of surface roughness and surface free energy parameters of oxide Al{sub 2}O{sub 3} and Ta{sub 2}O{sub 5} coatings and the possibility to separate the influence of such factors on the regularities and mechanisms of nano materials interactions with the biological objects.

  15. Impact of Dental Implant Surface Modifications on Osseointegration

    Science.gov (United States)

    Smeets, Ralf; Stadlinger, Bernd; Schwarz, Frank; Beck-Broichsitter, Benedicta; Jung, Ole; Precht, Clarissa; Kloss, Frank; Gröbe, Alexander; Heiland, Max

    2016-01-01

    Objective. The aim of this paper is to review different surface modifications of dental implants and their effect on osseointegration. Common marketed as well as experimental surface modifications are discussed. Discussion. The major challenge for contemporary dental implantologists is to provide oral rehabilitation to patients with healthy bone conditions asking for rapid loading protocols or to patients with quantitatively or qualitatively compromised bone. These charging conditions require advances in implant surface design. The elucidation of bone healing physiology has driven investigators to engineer implant surfaces that closely mimic natural bone characteristics. This paper provides a comprehensive overview of surface modifications that beneficially alter the topography, hydrophilicity, and outer coating of dental implants in order to enhance osseointegration in healthy as well as in compromised bone. In the first part, this paper discusses dental implants that have been successfully used for a number of years focusing on sandblasting, acid-etching, and hydrophilic surface textures. Hereafter, new techniques like Discrete Crystalline Deposition, laser ablation, and surface coatings with proteins, drugs, or growth factors are presented. Conclusion. Major advancements have been made in developing novel surfaces of dental implants. These innovations set the stage for rehabilitating patients with high success and predictable survival rates even in challenging conditions. PMID:27478833

  16. Impact of Dental Implant Surface Modifications on Osseointegration

    Directory of Open Access Journals (Sweden)

    Ralf Smeets

    2016-01-01

    Full Text Available Objective. The aim of this paper is to review different surface modifications of dental implants and their effect on osseointegration. Common marketed as well as experimental surface modifications are discussed. Discussion. The major challenge for contemporary dental implantologists is to provide oral rehabilitation to patients with healthy bone conditions asking for rapid loading protocols or to patients with quantitatively or qualitatively compromised bone. These charging conditions require advances in implant surface design. The elucidation of bone healing physiology has driven investigators to engineer implant surfaces that closely mimic natural bone characteristics. This paper provides a comprehensive overview of surface modifications that beneficially alter the topography, hydrophilicity, and outer coating of dental implants in order to enhance osseointegration in healthy as well as in compromised bone. In the first part, this paper discusses dental implants that have been successfully used for a number of years focusing on sandblasting, acid-etching, and hydrophilic surface textures. Hereafter, new techniques like Discrete Crystalline Deposition, laser ablation, and surface coatings with proteins, drugs, or growth factors are presented. Conclusion. Major advancements have been made in developing novel surfaces of dental implants. These innovations set the stage for rehabilitating patients with high success and predictable survival rates even in challenging conditions.

  17. Surface modification of magnesium hydroxide using vinyltriethoxysilane by dry process

    Science.gov (United States)

    Lan, Shengjie; Li, Lijuan; Xu, Defang; Zhu, Donghai; Liu, Zhiqi; Nie, Feng

    2016-09-01

    In order to improve the compatibility between magnesium hydroxide (MH) and polymer matrix, the surface of MH was modified using vinyltriethoxysilane (VTES) by dry process and the interfacial interaction between MH and VTES was also studied. Zeta potential measurements implied that the MH particles had better dispersion and less aggregation after modification. Sedimentation tests showed that the surface of MH was transformed from hydrophilic to hydrophobic, and the dispersibility and the compatibility of MH particles significantly improved in the organic phase. Scanning electronic microscopy (SEM), Transmission electron microscopy (TEM) and X-ray powder diffraction (XRD) analyses showed that a thin layer had formed on the surface of the modified MH, but did not alter the material's crystalline phase. Fourier transform infrared (FT-IR) spectra, X-ray photoelectron spectra (XPS) and Thermogravimetric analysis (TGA) showed that the VTES molecules bound strongly to the surface of MH after modification. Chemical bonds (Sisbnd Osbnd Mg) formed by the reaction between Si-OC2H5 and hydroxyl group of MH, also there have physical adsorption effect in the interface simultaneously. A modification mechanism of VTES on the MH surface by dry process was proposed, which different from the modification mechanism by wet process.

  18. Effects of Surface Modification on the Dispersion Property of VGCF

    Institute of Scientific and Technical Information of China (English)

    FU Yaqin; HAN Chunshao; NI Qingqing

    2009-01-01

    In view of the easy agglomeration issue of vapor grown carbon fiber (VGCF) and the poor interfacial adhesion between VGCF and matrix resin, two-step surface modification with hydrogen peroxide and concentrated nitric acid was performed on VGCF. The surface structure and dispersion of VGCF before and after modification were tested and analyzed by XRD, TGA, FTIR, UV-visible spectrum and SEM. Moreover, VGCF/SMPU composites were prepared via a solution mixing method taking shape memory polyurethane (SMPU) as matrix, and the mechanical properties of the composites were also tested. The graphite crystal structure of VGCF showed very little change af-ter modification, the concentration of oxygen-containing functional groups on the surface of VGCF was visibly in-creased, and the dispersion and dispersion stability of VGCF in organic solvent were also clearly improved. In the cross section of the VGCF/SMPU composites, the dispersion of VGCF in matrix and the VGCF-matrix interfacial adhesion observed through SEM were both enhanced to a certain extent after surface modification. The two-step surface modified VGCF had more obvious mechanical reinforcement effects on the composites than that of the pris-tine VGCF.

  19. Adsorption of Cationic Peptides to Solid Surfaces of Glass and Plastic

    DEFF Research Database (Denmark)

    Kristensen, Kasper; Henriksen, Jonas Rosager; Andresen, Thomas Lars

    2015-01-01

    Cationic membrane-active peptides have been studied for years in the hope of developing them into novel types of therapeutics. In this article, we investigate an effect that might have significant experimental implications for investigators who wish to study these peptides, namely, that the pepti......Cationic membrane-active peptides have been studied for years in the hope of developing them into novel types of therapeutics. In this article, we investigate an effect that might have significant experimental implications for investigators who wish to study these peptides, namely......, that the peptides adsorb to solid surfaces of glass and plastic. Specifically, we use analytical HPLC to systematically quantify the adsorption of the three cationic membraneactive peptides mastoparan X, melittin, and magainin 2 to the walls of commonly used glass and plastic sample containers. Our results show...... experiments on cationic membrane-active peptides. We conclude the article by discussing different strategies for reducing the experimental impact of these adsorption effects....

  20. Surface Modification of Hydroxyapatite by Using γ-aminopropyl Silane

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Surface modification of hydroxyapatite(HA) powder was performed with r-aminopropyl silane in toluent solvent. The modification effects were characterized by using XPS and FT-IR methods. The results indicated that the P2p electron binding energy of the modified HA decreases 0.4eV compared to that of HA. Furthermore, a new peak, 998cm-1 absorption appeared in IR differential spectra of modified HA and HA, which is due to a stretching vibration of structure P-O-Si, meaning that a direct covalent bonding between hydroxyl group on HA surface and the organic silane molecule was realized after modification, and the chemical bonding type was P-O-Si. The formation of the above structure suggested that the more effective interfacial adhesion between the modified HA and polymer matrix could be carried out.

  1. Grafting modification on the surface of titanium dioxide by polystyrene

    Institute of Scientific and Technical Information of China (English)

    Wei Wu; Shouci Lu; Jianfeng Chen; Lei Shao; CheeKing Tan

    2003-01-01

    Based on the technology of titanium dioxide grafting modification with polystyrene (PS), the modification mechanisms are studied and the polystyrene-grafting states on the surface of titanium dioxide have been set up. Under the synergistic actions of mechanical force, chemistry and heat, macromolecular free radicals of PS are created, at the same time, the O-O bonds of titanium dioxide are broken and the oxide free radicals produced, and the numbers of oxygen atom are increased and crystal lattice defects rich electrons are formed on the surface of titanium dioxide. The radical polymerization is the main reaction between PS and titanium dioxide and C-O bonds form in the process of modification. Multi-sites chemical adsorption also exists besides grafting between PS and titanium dioxide.

  2. Hydrophobically-associating cationic polymers as micro-bubble surface modifiers in dissolved air flotation for cyanobacteria cell separation.

    Science.gov (United States)

    Yap, R K L; Whittaker, M; Diao, M; Stuetz, R M; Jefferson, B; Bulmus, V; Peirson, W L; Nguyen, A V; Henderson, R K

    2014-09-15

    Dissolved air flotation (DAF), an effective treatment method for clarifying algae/cyanobacteria-laden water, is highly dependent on coagulation-flocculation. Treatment of algae can be problematic due to unpredictable coagulant demand during blooms. To eliminate the need for coagulation-flocculation, the use of commercial polymers or surfactants to alter bubble charge in DAF has shown potential, termed the PosiDAF process. When using surfactants, poor removal was obtained but good bubble adherence was observed. Conversely, when using polymers, effective cell removal was obtained, attributed to polymer bridging, but polymers did not adhere well to the bubble surface, resulting in a cationic clarified effluent that was indicative of high polymer concentrations. In order to combine the attributes of both polymers (bridging ability) and surfactants (hydrophobicity), in this study, a commercially-available cationic polymer, poly(dimethylaminoethyl methacrylate) (polyDMAEMA), was functionalised with hydrophobic pendant groups of various carbon chain lengths to improve adherence of polymer to a bubble surface. Its performance in PosiDAF was contrasted against commercially-available poly(diallyl dimethyl ammonium chloride) (polyDADMAC). All synthesised polymers used for bubble surface modification were found to produce positively charged bubbles. When applying these cationic micro-bubbles in PosiDAF, in the absence of coagulation-flocculation, cell removals in excess of 90% were obtained, reaching a maximum of 99% cell removal and thus demonstrating process viability. Of the synthesised polymers, the polymer containing the largest hydrophobic functionality resulted in highly anionic treated effluent, suggesting stronger adherence of polymers to bubble surfaces and reduced residual polymer concentrations.

  3. Surface modification of polymeric materials by cold atmospheric plasma jet

    Science.gov (United States)

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

    2014-09-01

    In this work we report the surface modification of different engineering polymers, such as, polyethylene terephthalate (PET), polyethylene (PE) and polypropylene (PP) by an atmospheric pressure plasma jet (APPJ). It was operated with Ar gas using 10 kV, 37 kHz, sine wave as an excitation source. The aim of this study is to determine the optimal treatment conditions and also to compare the polymer surface modification induced by plasma jet with the one obtained by another atmospheric pressure plasma source - the dielectric barrier discharge (DBD). The samples were exposed to the plasma jet effluent using a scanning procedure, which allowed achieving a uniform surface modification. The wettability assessments of all polymers reveal that the treatment leads to reduction of more than 40° in the water contact angle (WCA). Changes in surface composition and chemical bonding were analyzed by x-ray photoelectron spectroscopy (XPS) and Fourier-Transformed Infrared spectroscopy (FTIR) that both detected incorporation of oxygen-related functional groups. Surface morphology of polymer samples was investigated by Atomic Force Microscopy (AFM) and an increase of polymer roughness after the APPJ treatment was found. The plasma-treated polymers exhibited hydrophobic recovery expressed in reduction of the O-content of the surface upon rinsing with water. This process was caused by the dissolution of low molecular weight oxidized materials (LMWOMs) formed on the surface as a result of the plasma exposure.

  4. Modifications in structural, cation distribution and magnetic properties of {sup 60}Co gamma irradiated Li-ferrite

    Energy Technology Data Exchange (ETDEWEB)

    Mane, Maheshkumar L. [Department of Physics, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.) 431 004 (India); Shirsath, Sagar E., E-mail: shirsathsagar@hotmail.com [Department of Physics, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.) 431 004 (India); Dhage, Vinod N.; Jadhav, K.M. [Department of Physics, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad (M.S.) 431 004 (India)

    2011-09-15

    Highlights: {yields} Gamma irradiation induced defects in lithium ferrite. {yields} Modifications in structural and magnetic properties. {yields} Fe{sup 3+} changes to Fe{sup 2+} after gamma irradiation. - Abstract: Polycrystalline samples of Li{sub 0.5}Fe{sub 2.5}O{sub 4} ferrite precursor were prepared by conventional standard double sintering ceramic technique and then irradiated with three different doses of {sup 60}Co gamma rays. The crystal structure and phase orientation of the irradiated and unirradiated samples of Li{sub 0.5}Fe{sub 2.5}O{sub 4} ferrite was done by using X-ray diffraction technique at room temperature. The lattice parameter of the studied samples increased due to the formation of Fe{sup 2+} ions under the ionizing effect of gamma radiation. The strain in the materials due to the irradiation was calculated from XRD data. Scanning electron microscope (SEM) studies indicate that the irradiation causes amorphization, especially at the grain boundaries. The cation distribution was calculated from XRD data analysis. By using cation distribution structural parameters such as theoretical lattice constant, ionic radii of available sites and the oxygen parameter 'u' have been calculated. The estimated cation distribution and other structural parameters shows strong influence of gamma rays on polycrystalline Li-ferrite. The magnetic properties of irradiated and unirradiated lithium ferrite were performed by using pulse field hysteresis loop technique at room temperature. Electrical properties such as diffusion coefficient and dielectric properties were carried out with the influence of gamma irradiation. Activation energy of diffusion process decreased after irradiation. The increase of diffusion coefficient with increasing dose rate of gamma irradiation was reinforced by the increase of Fe{sup 2+} ions and the displacement of metal ions from its original sites under the effect of gamma irradiation.

  5. SURFACE-MODIFICATION OF FINE RED IRON OXIDE PIGMENT

    Institute of Scientific and Technical Information of China (English)

    Shuilin Zheng; Qinghui Zhang

    2003-01-01

    Surface-modification of fine red iron oxide pigment was carried out in an aqueous solution of sodium polyacrylate. The sedimentation time of modified samples in water increased from 1.05 to 264.4 hours while the particle size (d50) decreased from 1.09 to 0.85 μm, and the tinting strength increased from 100 to 115. The surface-modification as well as the dispersing and stabilizing mechanisms in aqueous solution of the samples were studied by means of IR,Thermal analysis and Zeta potential. The results showed that the modifier molecules acted on the surface of the particles by chemical and physical adsorption, and after the particles were dispersed in aqueous solution, endowing the particle surface with a relatively high negative Zeta potential, thus enhancing electrostatic and steric repulsion between particles for their effective stabilization.

  6. Advancing Sustainable Catalysis with Magnetite Surface Modification and Synthetic Applications

    Science.gov (United States)

    This article surveys the recent developments in the synthesis, surface modification, and synthetic applications of magnetitenanoparticles. The emergence of iron(II,III) oxide (triiron tetraoxide or magnetite; Fe3O4, or FeO•Fe2O3) nanoparticles as a sustainable support in heteroge...

  7. Ion-Induced Surface Modification of Magnetically Operated Contacts

    Directory of Open Access Journals (Sweden)

    Karen Arushanov

    2012-02-01

    Full Text Available A study has been made of permalloy (iron-nickel contacts of reed switches before and after ion-induced surface modification using atomic force and optical microscopy, Auger electron and X-ray photoelectron spectroscopy. It has been found that the formation of surface nitride layers enhances corrosion and erosion resistance of contacts. We proposed to produce such layers directly into sealed reed switches by means of pulsing glow-discharge nitrogen plasma.

  8. Chemical Modification Methods of Nanoparticles of Silicon Carbide Surface

    OpenAIRE

    Anton S. Yegorov; Vitaly S. Ivanov; Alexey V. Antipov; Alyona I. Wozniak; Kseniia V. Tcarkova.

    2015-01-01

    silicon carbide exhibits exceptional properties: high durability, high thermal conductivity, good heat resistance, low thermal expansion factor and chemical inactivity. Reinforcement with silicon carbide nanoparticles increases polymer’s tensile strength and thermal stability.Chemical methods of modification of the silicon carbide surface by means of variety of reagents from ordinary molecules to macromolecular polymers are reviewed in the review.The structure of silicon carbide surface layer...

  9. Surface modification for interaction study with bacteria and preosteoblast cells

    Science.gov (United States)

    Song, Qing

    Surface modification plays a pivotal role in bioengineering. Polymer coatings can provide biocompatibility and biofunctionalities to biomaterials through surface modification. In this dissertation, initiated chemical vapor deposition (iCVD) was utilized to coat two-dimensional (2D) and three-dimensional (3D) substrates with differently charged polyelectrolytes in order to generate antimicrobial and osteocompatible biomaterials. ICVD is a modified CVD technique that enables surface modification in an all-dry condition without substrate damage and solvent contamination. The free-radical polymerization allows the vinyl polymers to conformally coat on various micro- and nano-structured substrates and maintains the delicate structure of the functional groups. The vapor deposition of polycations provided antimicrobial activity to planar and porous substrates through destroying the negatively charged bacterial membrane and brought about high contact-killing efficiency (99.99%) against Gram-positive Bacillus subtilis and Gram-negative Escherichia coli. Additionally, the polyampholytes synthesized by iCVD exhibited excellent antifouling performance against the adhesion of Gram-positive Listeria innocua and Gram-negative E. coli in phosphate buffered saline (PBS). Their antifouling activities were attributed to the electrostatic interaction and hydration layers that served as physical and energetic barriers to prevent bacterial adhesion. The contact-killing and antifouling polymers synthesized by iCVD can be applied to surface modification of food processing equipment and medical devices with the aim of reducing foodborne diseases and medical infections. Moreover, the charged polyelectrolyte modified 2D polystyrene surfaces displayed good osteocompatibility and enhanced osteogenesis of preosteoblast cells than the un-modified polystyrene surface. In order to promote osteoinduction of hydroxyapatite (HA) scaffolds, bioinspired polymer-controlled mineralization was conducted

  10. Improved LWR Cladding Performance by EPD Surface Modification Technique

    Energy Technology Data Exchange (ETDEWEB)

    Corradini, Michael; Sridharan, Kumar

    2012-11-26

    This project will utilize the electro-phoretic deposition technique (EPD) in conjunction with nanofluids to deposit oxide coatings on prototypic zirconium alloy cladding surfaces. After demonstrating that this surface modification is reproducible and robust, the team will subject the modified surface to boiling and corrosion tests to characterize the improved nucleate boiling behavior and superior corrosion performance. The scope of work consists of the following three tasks: The first task will employ the EPD surface modification technique to coat the surface of a prototypic set of zirconium alloy cladding tube materials (e.g. Zircaloy and advanced alloys such as M5) with a micron-thick layer of zirconium oxide nanoparticles. The team will characterize the modified surface for uniformity using optical microscopy and scanning-electron microscopy, and for robustness using standard hardness measurements. After zirconium alloy cladding samples have been prepared and characterized using the EPD technique, the team will begin a set of boiling experiments to measure the heat transfer coefficient and critical heat flux (CHF) limit for each prepared sample and its control sample. This work will provide a relative comparison of the heat transfer performance for each alloy and the surface modification technique employed. As the boiling heat transfer experiments begin, the team will also begin corrosion tests for these zirconium alloy samples using a water corrosion test loop that can mimic light water reactor (LWR) operational environments. They will perform extended corrosion tests on the surface-modified zirconium alloy samples and control samples to examine the robustness of the modified surface, as well as the effect on surface oxidation

  11. Natural bone-like biomimetic surface modification of titanium

    Science.gov (United States)

    Yoon, Il-Kyu; Hwang, Ji-Young; Jang, Won-Cheoul; Kim, Hae-Won; Shin, Ueon Sang

    2014-05-01

    An implantable metallic surface consisting of titanium (Ti) was modified with natural bone-mimicking CNT-Gelatin-HA nanohybrids to create a new surface with similar properties to the surrounding bone tissue in terms of the chemical constitution, nanotopography, wettability, and biocompatibility. The biomimetic surface modification was achieved through the covalent immobilization of carbon nanotubes (CNTs) onto the Ti surface, the covalent tethering of gelatin molecules onto the CNT surface, and then the deposition of hydroxyl apatite (HA) crystals onto the gelatin-tethered CNTs in SBF solution. The SEM microscopic images demonstrated that the modified Ti surface continually maintained a fibrous structure of CNTs, but that the CNT fibers were hybridized with gelatin and HA in a multi-core-shell structure of similar constitution to that of the collagen fibers of natural bone. The new surface of the Ti substrates showed significantly higher mechanical properties and favorable wettability and biocompatibility.

  12. SDS-PAGE and IR spectroscopy to evaluate modifications in the viral protein profile induced by a cationic porphyrinic photosensitizer.

    Science.gov (United States)

    Costa, Liliana; Esteves, Ana Cristina; Correia, António; Moreirinha, Catarina; Delgadillo, Ivonne; Cunha, Ângela; Neves, Maria G P S; Faustino, Maria A F; Almeida, Adelaide

    2014-12-01

    Reactive oxygen species can be responsible for microbial photodynamic inactivation due to its toxic effects, which include severe damage to proteins, lipids and nucleic acids. In this study, the photo-oxidative modifications of the proteins of a non-enveloped T4-like bacteriophage, induced by the cationic porphyrin 5,10,15-tris(1-methylpyridinium-4-yl)-20-(pentafluorophenyl)porphyrin tri-iodide were evaluated. Two methods were used: sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and infrared spectroscopy. SDS-PAGE analysis showed that the phage protein profile was considerably altered after photodynamic treatment. Seven protein bands putatively corresponding to capsid and tail tube proteins were attenuated and two other were enhanced. Infrared spectroscopy confirmed the time-dependent alteration on the phage protein profile detected by SDS-PAGE, indicative of a response to oxidative damage. Infrared analysis showed to be a promising and rapid screening approach for the analysis of the modifications induced on viral proteins by photosensitization. In fact, one single infrared spectrum can highlight the changes induced to all viral molecular structures, overcoming the delays and complex protocols of the conventional methods, in a much simple and cost effective way.

  13. Surface modification on silicon with chitosan and biological research

    Energy Technology Data Exchange (ETDEWEB)

    Lue Xiaoying; Cui Wei; Huang Yan; Zhao Yi [State Key Laboratory of Bioelectronics, Southeast University, Nanjing, 210096 (China); Wang Zhigong, E-mail: luxy@seu.edu.c [Institute of RF- and OE-ICs, Southeast University, Nanjing, 210096 (China)

    2009-08-15

    The aim of the present study was to investigate the effect of chitosan modification of silicon (Si) on protein adsorption, cell adhesion and cell proliferation. Chitosan was first immobilized on the Si surface through a (3-aminopropyl)triethoxysilane (APTES) bridge. The surface was then characterized by contact angle measurement, atomic force microscopy (AFM), x-ray photoelectron spectroscopy (XPS) and energy dispersive x-ray spectroscopy (EDX). The amount of protein adsorbed on the native Si and chitosan-modified Si surface was evaluated by a modified Coomassie brilliant blue (CBB) protein assay. The adhesion and proliferation behavior of L-929 and pc12 cells were then assessed by microscopy and methylthiazoltetrazolium (MTT) tests. The results showed that the chitosan modification could resist protein adsorption and inhibit the adhesion and proliferation of two kinds of cells on Si.

  14. Effect of surface modification on semiconductor nanocrystal fluorescence lifetime.

    Science.gov (United States)

    Ruedas-Rama, Maria J; Orte, Angel; Hall, Elizabeth A H; Alvarez-Pez, Jose M; Talavera, Eva M

    2011-04-04

    Semiconductor nanocrystals, namely, quantum dots (QDs), present a set of unique photoluminescence properties, which has led to increased interest in using them as advantageous alternatives to conventional organic dyes. Many applications of QDs involve surface modification to enhance the solubility or biocompatibility of the QDs. One of the least exploited properties of QDs is the very long photoluminescence lifetime that usually has complex kinetics owing to the effect of quantum confinement. Herein, we describe the effect of different surface modifications on the photoluminescence decay kinetics of QDs. The different surface modifications were carefully chosen to provide lipophilic or water-soluble QDs with either positive or negative surface net charges. We also survey the effect on the QD lifetime of several ligands that interact with the QD surface, such as organic chromophores or fluorescent proteins. The results obtained demonstrate that time-resolved fluorescence is a useful tool for QD-based sensing to set the basis for the development of time-resolved-based nanosensors.

  15. Inhibition of biofouling by modification of forward osmosis membrane using quaternary ammonium cation.

    Science.gov (United States)

    Park, Kang-Hee; Yu, Sang-Hyun; Kim, Han-Shin; Park, Hee-Deung

    2015-01-01

    In the operation of the forward osmosis (FO) process, biofouling of the membrane is a potentially serious problem. Development of an FO membrane with antibacterial properties could contribute to a reduction in biofouling. In this study, quaternary ammonium cation (QAC), a widely used biocidal material, was conjugated with a silane coupling agent (3-(trimethoxysilyl)-propyldimethyloctadecyl ammonium chloride) and used to modify an FO membrane to confer antibacterial properties. Fourier transform infrared spectroscopy (FT-IR) demonstrated that the conjugated QAC was successfully immobilized on the FO membrane via covalent bonding. Bacterial viability on the QAC-modified membrane was confirmed via colony count method and visualized via bacterial viability assay. The QAC membrane decreased the viability of Escherichia coli to 62% and Staphylococcus aureus to 77% versus the control membrane. Inhibition of biofilm formation on the QAC modified membrane was confirmed via anti-biofilm tests using the drip-flow reactor and FO unit, resulting in 64% and 68% inhibition in the QAC-modified membrane against the control membrane, respectively. The results demonstrate the effectiveness of the modified membrane in reducing bacterial viability and inhibiting biofilm formation, indicating the potential of QAC-modified membranes to decrease operation costs incurred by biofouling.

  16. Experimental Study on Material Surface Modification of Tool Steel

    Institute of Scientific and Technical Information of China (English)

    沈丽如; 童洪辉; 王珂; 铁军; 孙爱萍

    2002-01-01

    This paper presents the surface temperature behavior of M42 high-speed tool steel samples during N+ implantation in an industrialized GLZ-100 metal-ion implantation machine. A detail study has been made on the parameters ofN+ implantation. Optimized technical parameters have been presented. The microhardness of the sample surface implanted under these parameters has been increased by a factor of 2.3, and the wear-resistance has been improved by about 5.4 times.The research on the mechanism of surface modification of M42 steel by nitrogen ion implantation has also been made.

  17. Effects of aluminium surface morphology and chemical modification on wettability

    DEFF Research Database (Denmark)

    Rahimi, Maral; Fojan, Peter; Gurevich, Leonid;

    2014-01-01

    Aluminium alloys are some of the predominant metals in industrial applications such as production of heat exchangers, heat pumps. They have high heat conductivity coupled with a low specific weight. In cold working conditions, there is a risk of frost formation on the surface of aluminium...... in the presence of water vapour, which can lead to the deterioration of equipment performance. This work addresses the methods of surface modification of aluminium and their effect of the underlying surface morphology and wettability, which are the important parameters for frost formation. Three groups of real...

  18. Design and Application of Surface Modification at Molecular Scale

    Institute of Scientific and Technical Information of China (English)

    CHEN Miao; XUE Qun-Ji; ZHOU Feng; GUAN Fei; LIU Wei-Min

    2004-01-01

    The structuring of surfaces on a nanoscale level-both chemically and topographically has become an increasingly relevant field of research in nanotechnology with widespread application potential in various fields of science ( e. g.surface engineering, electronics, biotechnology, optics). Two examples on surface modification at molecular scale with self-assembly monolayers are shown: ( 1 ) Chemically attaching ultra-thin polymer films through the self-assembly of silane fictionalized copolymer have been approved in this article. (2) The patterned films with microstructures on different substrates have been prepared through micro-contact printing technique and electro polymerization.

  19. Modification of Textile Materials' Surface Properties Using Chemical Softener

    Directory of Open Access Journals (Sweden)

    Jurgita KOŽENIAUSKIENĖ

    2011-03-01

    Full Text Available In the present study the effect of technological treatment involving the processes of washing or washing and softening with chemical cationic softener "Surcase" produced in Great Britain on the surface properties of cellulosic textile materials manufactured from cotton, bamboo and viscose spun yarns was investigated. The changes in textile materials surface properties were evaluated using KTU-Griff-Tester device and FEI Quanta 200 FEG scanning electron microscope (SEM. It was observed that the worst hand properties and the higher surface roughness are observed of cotton materials if compared with those of bamboo and viscose materials. Also, it was shown that depending on the material structure the handle parameters of knitted materials are the better than the ones of woven fabrics.http://dx.doi.org/10.5755/j01.ms.17.1.249

  20. Induction of surface modification of polytetrafluoroethylene with proton ion beams

    Energy Technology Data Exchange (ETDEWEB)

    Noh, I. S.; Kim, H. R.; Choi, Y. J.; Park, H. S. [Seoul National Univ. of Technology, Seoul (Korea, Republic of)

    2007-04-15

    Cardiovascular disease is one of the leading causes of the death in the USA and developed countries. More than 570,000 artery bypass graft surgeries per USA are performed each year, though percutaneous devices have abounded in extreme cases. Based on the surgery follow-ups, large diameter expanded polytetrafluoroethylene (ePTFE) (>5 mm) are clinically employed with good results but its clinical applications in smaller vessels is still problematic due to thrombosis and neointima formation. Achievement of high patency grafts has been to some extent achieved by numerous methods of surface modification techniques, but its results are less than its initial hopes. As examples, endothelial cells coated on the luminal surface of ePTFE has demonstrated limited success after recirculation. Surface modifications of PTFE film with either argon ion beam or UV light from Xe-excimer lamp were reported to increase its interaction with vascular endothelial cell. Surface modification of poly(lactide-co-glycolide)[PLGA] is also very important in tissue engineering, in where induction of its initial high cellular adhesion and spreading is a critical step for development of tissue engineering medical products. We previously reported tissue engineering of the hybrid ePTFE scaffold by seeding smooth muscle cells and subsequently evaluation of its tissue regeneration behaviors and stabilities with circulation of pulsatile flow. To improve its tissue engineering more quickly, we here performed surface modification of ePTFE and porous PLGA scaffold and evaluated its subsequent chemical and biological properties after treating its surface with low energy ion beams. The porous ePTFE was prepared in a round shape (diameter = 1 cm) and dried after organic solvent extraction for ion beam treatment. Another porous PLGA layers (d = 1 cm, t = 1 cm with approximately 92% porosity) were fabricated and treated its surface by irradiating low energy either nitrogen or argon ion beams (1 keV, 1x1015 ions

  1. Surface modification of g-Al2O3 by sodium ions

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    1H/23Na double resonance NMR techniques were employed to study the modification of surface hydroxyls on g-Al2O3 by sodium ions. 1H→23Na cross polarization (CP) experiment can resolve three kinds of sodium cations that are closely associated with surface hydroxyl groups, while the signal of deposited salt-Na2CO3, which is not connected to surface hydroxyl groups, is completely suppressed. 1H{23Na} spin echo double resonance experiments reveal the surface modification in more detail. At low Na+ coverage (5%, 10%), the acidic hydroxyl groups are preferentially coordinated with sodium ions, while both the acidic and the basic hydroxyl groups are accessible for sodium ions at high coordination that causes proton of the OH groups to be easily dissolved, which is evidenced by the fact that with calcination temperature of the catalysts increasing, the acidic hydroxyl groups are preferentially removed and only the basic hydroxyl groups remain when the calcination temperature is raised to 600℃.

  2. Tribological effects of polymer surface modification through plastic deformation

    Indian Academy of Sciences (India)

    K O Low; K J Wong

    2011-12-01

    The efficacy of using polymers in cylindrical applications depends closely on its surface friction and wear characteristics. In this regard, a surface modification technique through plastic deformation has been implemented. Roller burnishing is commonly used to improve the surface quality of non-ferrous surfaces, but no work showed concern about roller burnishing as a polymer surface treatment process. The objective of the present work is to investigate the influence of burnishing force and burnishing speed on the friction and wear performance of acetal homopolymer and polyurethane under dry and lubricated sliding conditions. The results reveal that the coefficient of friction and wear rate decreased to a minimum value and then increased as higher burnishing force and speed were applied. It was shown that roller burnishing had favourable prospective to be utilized as a valuable polymer surface treatment technique.

  3. Surface Modification of Nitinol by Chemical and Electrochemical Etching

    Science.gov (United States)

    Yang, Zhendi; Wei, Xiaojin; Cao, Peng; Gao, Wei

    2013-07-01

    In this paper, Nitinol, an equiatomic binary alloy of nickel and titanium, was surface modified for its potential biomedical applications by chemical and electrochemical etching. The main objective of the surface modification is to reduce the nickel content on the surface of Nitinol and simultaneously to a rough surface microstructure. As a result, better biocompatibility and better cell attachment would be achieved. The effect of the etching parameters was investigated, using scanning electron microscopy (SEM) equipped with energy dispersive X-ray spectrometry (EDX) and X-ray photoelectron spectrometry (XPS). The corrosion property of modified Nitinol surfaces was investigated by electrochemical work station. After etching, the Ni content in the surface layer has been reduced and the oxidation of Ti has been enhanced.

  4. Surface modification of promising cerium oxide nanoparticles for nanomedicine applications

    KAUST Repository

    Nanda, Himansu Sekhar

    2016-11-14

    Cerium oxide nanoparticles (CNPs) or nanoceria have emerged as a potential nanomedicine for the treatment of several diseases such as cancer. CNPs have a natural tendency to aggregate or agglomerate in their bare state, which leads to sedimentation in a biological environment. Since the natural biological environment is essentially aqueous, nanoparticle surface modification using suitable biocompatible hydrophilic chemical moieties is highly desirable to create effective aqueous dispersions. In this report, (6-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-hexyl)triethoxysilane was used as a functional, biocompatible organosilane to modify the surface of CNPs to produce promising nanoparticles which open substantial therapeutic avenues. The surface modified nanoparticles were produced in situ via an ammonia-induced ethylene glycol-assisted precipitation method and were characterized using complimentary characterization techniques. The interaction between the functional moiety and the nanoparticle was studied using powerful cross polarization/magic angle sample spinning solid state nuclear magnetic resonance spectroscopy. The surface-modified nanoparticles were extremely small and demonstrated a significant improvement in aqueous dispersibility. Moreover, the existence of a strong ionic coordination between the functional moiety and the surface of the nanoparticle was realised, indicating that the surface modified nanoceria are stable and that the nanoparticles should demonstrate an enhanced circulation time in a biological environment. The surface modification approach should be promising for the production of CNPs for nanomedicine applications. © The Royal Society of Chemistry.

  5. Improved chemical and electrochemical stability of perovskite oxides with less reducible cations at the surface

    Science.gov (United States)

    Tsvetkov, Nikolai; Lu, Qiyang; Sun, Lixin; Crumlin, Ethan J.; Yildiz, Bilge

    2016-09-01

    Segregation and phase separation of aliovalent dopants on perovskite oxide (ABO3) surfaces are detrimental to the performance of energy conversion systems such as solid oxide fuel/electrolysis cells and catalysts for thermochemical H2O and CO2 splitting. One key reason behind the instability of perovskite oxide surfaces is the electrostatic attraction of the negatively charged A-site dopants (for example, ) by the positively charged oxygen vacancies () enriched at the surface. Here we show that reducing the surface concentration improves the oxygen surface exchange kinetics and stability significantly, albeit contrary to the well-established understanding that surface oxygen vacancies facilitate reactions with O2 molecules. We take La0.8Sr0.2CoO3 (LSC) as a model perovskite oxide, and modify its surface with additive cations that are more and less reducible than Co on the B-site of LSC. By using ambient-pressure X-ray absorption and photoelectron spectroscopy, we proved that the dominant role of the less reducible cations is to suppress the enrichment and phase separation of Sr while reducing the concentration of and making the LSC more oxidized at its surface. Consequently, we found that these less reducible cations significantly improve stability, with up to 30 times faster oxygen exchange kinetics after 54 h in air at 530 °C achieved by Hf addition onto LSC. Finally, the results revealed a `volcano' relation between the oxygen exchange kinetics and the oxygen vacancy formation enthalpy of the binary oxides of the additive cations. This volcano relation highlights the existence of an optimum surface oxygen vacancy concentration that balances the gain in oxygen exchange kinetics and the chemical stability loss.

  6. Contribution of hydrophobic/hydrophilic modification on cationic chains of poly(ε-caprolactone)-graft-poly(dimethylamino ethylmethacrylate) amphiphilic co-polymer in gene delivery.

    Science.gov (United States)

    Han, Shangcong; Wan, Haiying; Lin, Daoshu; Guo, Shutao; Dong, Hongxu; Zhang, Jianhua; Deng, Liandong; Liu, Ruming; Tang, Hua; Dong, Anjie

    2014-02-01

    Nanoparticles (NPs) assembled from amphiphilic polycations have been certified as potential carriers for gene delivery. Structural modification of polycation moieties may be an efficient route to further enhance gene delivery efficiency. In this study two electroneutral monomers with different hydrophobicities, 2-hydroxyethyl methacrylate (HEMA) and 2-hydroxyethyl acrylate (HEA), were incorporated into the cationic poly(dimethylamino ethyl methacrylate) (PDMAEMA) side-chains of amphiphilic poly(ε-caprolactone)-graft-poly(dimethylamino ethylmethacrylate) (PCD) by random co-polymerization, to obtain poly(ε-caprolactone)-graft-poly(dimethylamino ethyl methacrylate-co-2-hydroxyethyl methacrylate) (PCD-HEMA) and poly(ε-caprolactone)-graft-poly(dimethylamino ethyl methacrylate-co-2-hydroxyethyl acrylate) (PCD-HEA). Minimal HEA or HEMA moieties in PDMAEMA do not lead to statistically significant changes in particle size, zeta potential, DNA condensation properties and buffering capacity of the naked NPs. However, the incorporation of HEMA and HEA lead to reductions and increases, respectively, in the surface hydrophilicity of the naked NPs and NPs/DNA complexes, which was confirmed by water contact angle assay. These simple modifications of PDMAEMA with HEA and HEMA moieties significantly affect the gene transfection efficiency on HeLa cells in vitro: PCD-HEMA NP/DNA complexes show a much higher transfection efficiency than PCD NPs/DNA complexes, while PCD-HEA NPs/DNA complexes show a lower transfection efficiency than PCD NP/DNA complexes. Fluorescence activated cell sorter and confocal laser scanning microscope results indicate that the incorporation of hydrophobic HEMA moieties facilitates an enhancement in both cellular uptake and endosomal/lysosomal escape, leading to a higher transfection efficiency. Moreover, the process of endosomal/lysosomal escape confirmed in our research that PCD and its derivatives do not just rely on the proton sponge mechanism, but also

  7. A REVIEW OF OXYGEN-CONTAINING SURFACE GROUPS AND SURFACE MODIFICATION OF ACTIVATED CARBON

    Institute of Scientific and Technical Information of China (English)

    WU Yongwen; LI Zhong; XI Hongxia; XIA Qibin

    2004-01-01

    This review focused on the recent reports related to the function, characterization and modification of oxygen-containing surface groups of activated carbon (AC). The Oxygen-containing surface groups were briefly described, and the most frequently used techniques for characterization of the oxygen-containing surface groups on ACs were also briefly stated. A detailed discussion of the effects of the oxygen-containing surface groups on the adsorptive capacity of AC was given. The recent progresses in modification of the oxygen-containing surface groups of AC were also reviewed.

  8. Surface chemical modification of fullerene by mechanochemical treatment

    Science.gov (United States)

    Todorović Marković, B.; Jokanović, V.; Jovanović, S.; Kleut, D.; Dramićanin, M.; Marković, Z.

    2009-06-01

    In this study different encapsulating agents have been used for chemical modification of fullerenes. Fullerenes have reacted with tetrahydrofuran, sodium dodecyl sulfate, sodium dodecylbenzene sulfonate and ethylene vinyl acetate-ethylene vinyl versatate at room temperature under mechanical milling. The obtained powder has been dispersed in water by ultrasonication. The fullerene based colloids have been characterized by UV-vis, FTIR, Raman spectroscopy and atomic force microscopy. FTIR and Raman analysis have shown the presence of C 60 after surface functionalization.

  9. Surface modification of poly(dimethylsiloxane) for microfluidic assay applications

    Energy Technology Data Exchange (ETDEWEB)

    Seguin, Christine; McLachlan, Jessica M.; Norton, Peter R. [Department of Chemistry, University of Western Ontario, 1151 Richmond St., London, ON, N6A 5B7 (Canada); Lagugne-Labarthet, Francois, E-mail: flagugne@uwo.ca [Department of Chemistry, University of Western Ontario, 1151 Richmond St., London, ON, N6A 5B7 (Canada)

    2010-02-01

    The surface of a poly(dimethylsiloxane) (PDMS) film was imparted with patterned functionalities at the micron-scale level. Arrays of circles with diameters of 180 and 230 {mu}m were functionalized using plasma oxidation coupled with aluminum deposition, followed by silanization with solutions of 3-aminopropyltrimethoxy silane (3-APTMS) and 3-mercaptopropyltrimethoxy silane (3-MPTMS), to obtain patterned amine and thiol functionalities, respectively. The modification of the samples was confirmed using X-ray photoelectron spectroscopy (XPS), gold nanoparticle adhesion coupled with optical microscopy, as well as by derivatization with fluorescent dyes. To further exploit the novel surface chemistry of the modified PDMS, samples with surface amine functionalities were used to develop a protein assay as well as an array capable of cellular capture and patterning. The modified substrate was shown to successfully selectively immobilize fluorescently labeled immunoglobulin G (IgG) by tethering Protein A to the surface, and, for the cellular arrays, C2C12 rat endothelial cells were captured. Finally, this novel method of patterning chemical functionalities onto PDMS has been incorporated into microfluidic channels. Finally, we demonstrate the in situ chemical modification of the protected PDMS oxidized surface within a microfluidic device. This emphasizes the potential of our method for applications involving micron-scale assays since the aluminum protective layer permits to functionalize the oxidized PDMS surface several weeks after plasma treatment simply after etching away the metallic thin film.

  10. The effect of substrate modification on microbial growth on surfaces

    CERN Document Server

    Brown, A A

    1998-01-01

    The principle aim of the program was to produce a novel, non-leaching antimicrobial surface for commercial development and future use in the liquid food packaging industry. Antimicrobial surfaces which exist presently have been produced to combat the growth of prokaryotic organisms and usually function as slow release systems. A system which could inhibit eukaryotic growth without contaminating the surrounding 'environment' with the inhibitor was considered of great commercial importance. The remit of this study was concerned with creating a surface which could control the growth of eukaryotic organisms found in fruit juice with particular interest in the yeast, Saccharomyces cerevisiae. Putative antimicrobial surfaces were created by the chemical modification of the test substrate polymers; nylon and ethylvinyl alcohol (EVOH). Surfaces were chemically modified by the covalent coupling of antimicrobial agents known to be active against the yeast Saccharomyces cerevisiae as ascertained by the screening process...

  11. Ultrasound enhanced plasma surface modification at atmospheric pressure

    DEFF Research Database (Denmark)

    Kusano, Yukihiro; Singh, Shailendra Vikram; Norrman, Kion

    Atmospheric pressure plasma treatment can be highly enhanced by simultaneous high-power ultrasonic irradiation onto the treating surface. It is because ultrasonic waves with a sound pressure level (SPL) above approximately 140 dB can reduce the thickness of a boundary gas layer between the plasma...... and the material surface, and thus many reactive species generated in the plasma can reach the surface before inactivated, and be efficiently utilized for surface modification. In the present work polyester plates are treated using a dielectric barrier discharge (DBD) and a gliding arc at atmospheric pressure...... irradiation, the water contact angle dropped markedly, and tended to decrease furthermore at higher power. The ultrasonic irradiation during the plasma treatment consistently improved the wettability. Oxygen containing polar functional groups were introduced at the surface by the plasma treatment...

  12. Role of water in polymer surface modification using organosilanes

    Science.gov (United States)

    Thallapalle, Pradeep Kumar; Zhang Newby, Bi-Min

    2002-03-01

    In general, polymers exhibit excellent bulk properties but may not possess specific surface properties for successful applications in biomaterials and nanotechnology. Surface modification of polymers with the self-assembled monolayers (SAMs) of organosilanes - ‘Silanization’ - is an attractive approach to alter surface properties without altering the polymer’s desired bulk properties. However, a pretreatment such as exposure to UV/O or plasma is normally required to generate active surface groups prior to silanization. These pretreatments cause undesirable surface changes such as severe surface roughening and excessive surface damage. Recent studies in silanization suggest that the presence of water or OH groups on the surface is essential to form SAMs. In this study we investigated the importance of surface water layer and OH groups in the formation of SAMs for a variety of polymers. The pre and post-modified polymers were examined using fourier transform infrared spectrometry, scanning probe microscopy and contact angle measurements. The results show that organosilanes can be grafted to a polymer surface as long as a water layer can be physisorbed to the surface or the polymer itself contains OH groups. However the monolayers formed are less organized compared to those formed on silicon wafers due to the amorphous nature of the polymers.

  13. Hemocompatible surface of electrospun nanofibrous scaffolds by ATRP modification

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Wenjie [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Feng, Yakai, E-mail: yakaifeng@hotmail.com [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Key Laboratory of Systems Bioengineering of Ministry of Education, Tianjin University, Tianjin 300072 (China); Tianjin University-Helmholtz-Zentrum Geesthacht, Joint Laboratory for Biomaterials and Regenerative Medicine, Weijin Road 92, 300072 Tianjin (China); Wang, Heyun [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); School of Chemistry and Chemical Engineering, Shihezi University, Shihezi 832002 (China); Yang, Dazhi [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); An, Bo [Department of Orthopedics, Affiliated Hospital of Logistics University of Chinese People' s Armed Police Force, Tianjin 300162 (China); Zhang, Wencheng [Department of Physiology and Pathophysiology, Logistics University of Chinese People' s Armed Police Force, Tianjin 300162 (China); Khan, Musammir [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Guo, Jintang [School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Tianjin University-Helmholtz-Zentrum Geesthacht, Joint Laboratory for Biomaterials and Regenerative Medicine, Weijin Road 92, 300072 Tianjin (China)

    2013-10-15

    The electrospun scaffolds are potential application in vascular tissue engineering since they can mimic the nano-sized dimension of natural extracellular matrix (ECM). We prepared a fibrous scaffold from polycarbonateurethane (PCU) by electrospinning technology. In order to improve the hydrophilicity and hemocompatibility of the fibrous scaffold, poly(ethylene glycol) methacrylate (PEGMA) was grafted onto the fiber surface by surface-initiated atom transfer radical polymerization (SI-ATRP) method. Although SI-ATRP has been developed and used for surface modification for many years, there are only few studies about the modification of electrospun fiber by this method. The modified fibrous scaffolds were characterized by SEM, Fourier transform infrared (FTIR), and X-ray photoelectron spectroscopy (XPS). The scaffold morphology showed no significant difference when PEGMA was grafted onto the scaffold surface. Based on the water contact angle measurement, the surface hydrophilicity of the scaffold surface was improved significantly after grafting hydrophilic PEGMA (P = 0.0012). The modified surface showed effective resistance for platelet adhesion compared with the unmodified surface. Activated partial thromboplastin time (APTT) of the PCU-g-PEGMA scaffold was much longer than that of the unmodified PCU scaffold. The cyto-compatibility of electrospun nanofibrous scaffolds was tested by human umbilical vein endothelial cells (HUVECs). The images of 7-day cultured cells on the scaffold surface were observed by SEM. The modified scaffolds showed high tendency to induce cell adhesion. Moreover, the cells reached out pseudopodia along the fibrous direction and formed a continuous monolayer. Hemolysis test showed that the grafted chains of PEGMA reduced blood coagulation. These results indicated that the modified electrospun nanofibrous scaffolds were potential application as artificial blood vessels. Highlights: • Electrospun nanofibrous scaffolds were successfully

  14. Reduction-induced surface modification of human hair.

    Science.gov (United States)

    Kamath, Yash K; Ruetsch, Sigrid B

    2010-01-01

    A microfluorometric method has been developed to characterize lipid removal or "delipidation" of the human hair cuticula during light exposure and chemical grooming processes such as oxidation (bleaching) and reduction. In the case of photochemical and chemical oxidation, lipid removal ("delipidation" of the F-layer or lipid-layer) from the outer beta-layer of the exposed scale faces and generation of cysteic acid groups occurs. This "delipidation," which ultimately results in "acidification" of the scale faces, leading to a change in surface chemistry from hydrophobic to hydrophilic, can be detected and quantified by microfluorometry by tagging, e.g., with the cationic fluorochrome Rhodamine B. In the case of reduction, similar tagging of the acid sites on the scale faces is possible, but this time, Rhodamine B reacts with the mixed disulfide containing a carboxyl group that will be ionized above a pH of about 4. In addition to this, we have shown by microfluorometric scanning that the negative charges generated in the cuticle surface can be used to bind low-molecular-weight quaternary conditioners. This process can be considered as "relipidation" or "refatting" of the scale faces. We have shown in earlier studies (1) that this entire process of oxidation-induced "delipidation" and subsequent "relipidation" of the acidic scale faces with a cationic conditioning molecule can also be reliably quantified by X-ray photoelectron spectroscopy (XPS). Furthermore, single-fiber wettability scanning using the Wilhelmy technique, which is highly sensitive to any changes in surface chemistry, is well-suited to detect and characterize treatment-induced changes in the chemical nature of the hair surface from hydrophobic to hydrophilic.

  15. Self-Assembled Fluorinated Organogelators for Surface Modification

    Directory of Open Access Journals (Sweden)

    Anilkumar Raghavanpillai

    2012-03-01

    Full Text Available A new class of alkyl- and perfluoroalkyl-containing urea and amide derivatives was synthesized from amino acid derivatives. Most of these compounds showed excellent gelation behavior in organic solvents at low concentrations. A few organogelators selected from the initial screening were used for surface modification of fibrous substrates to create hydrophobic and oleophobic composites. The hydrophobic and oleophobic behaviors of these composites were ascribed to a combination of increased surface roughness and the alkyl/fluorinated functionalities present in the gelator backbone.

  16. Surface Modification of Textured Dielectrics and Their Wetting Behavior

    Science.gov (United States)

    Kumar, Vijay; Dhillon, Ajaypal Singh; Sharma, Niti Nipun

    2017-02-01

    Controlling the wettability on dielectric materials is a classical topic in surface engineering. Surface texturing and deposition of self-assembled monolayers (SAMs) are major approaches to achieve lower or higher water contact angle ( θ c) and thereby making surface less or more wettable (more hydrophobic). Dielectric surfaces wetting has been engineered by surface modification and has been shown to achieve θ c to a maximum of 120° ± 5°. Further improvement in θ c to an extent greater than 150° ± 5° is desired to render the surface superhydrophobic. We report in this work an achievement of θ c > 150° ± 5° by combining the plasma-treated surface and octadecyltrichlorosilane (OTS) SAMs deposition on dielectrics, and this had been shown on dielectric ranging from low- k to high- k values. The improvement in wetting behavior and quality of dielectric surface with monolayer on plasma-treated surfaces are (is) investigated and characterized using atomic-force microscope (AFM), scanning electron microscope (SEM), contact angle goniometer, and Raman spectroscopy and x-ray photoelectron spectroscopy (XPS) and are compared with untreated dielectric surface with OTS monolayers.

  17. Surface Modification of Textured Dielectrics and Their Wetting Behavior

    Science.gov (United States)

    Kumar, Vijay; Dhillon, Ajaypal Singh; Sharma, Niti Nipun

    2017-01-01

    Controlling the wettability on dielectric materials is a classical topic in surface engineering. Surface texturing and deposition of self-assembled monolayers (SAMs) are major approaches to achieve lower or higher water contact angle (θ c) and thereby making surface less or more wettable (more hydrophobic). Dielectric surfaces wetting has been engineered by surface modification and has been shown to achieve θ c to a maximum of 120° ± 5°. Further improvement in θ c to an extent greater than 150° ± 5° is desired to render the surface superhydrophobic. We report in this work an achievement of θ c > 150° ± 5° by combining the plasma-treated surface and octadecyltrichlorosilane (OTS) SAMs deposition on dielectrics, and this had been shown on dielectric ranging from low-k to high-k values. The improvement in wetting behavior and quality of dielectric surface with monolayer on plasma-treated surfaces are (is) investigated and characterized using atomic-force microscope (AFM), scanning electron microscope (SEM), contact angle goniometer, and Raman spectroscopy and x-ray photoelectron spectroscopy (XPS) and are compared with untreated dielectric surface with OTS monolayers.

  18. Hemocompatible surface of electrospun nanofibrous scaffolds by ATRP modification.

    Science.gov (United States)

    Yuan, Wenjie; Feng, Yakai; Wang, Heyun; Yang, Dazhi; An, Bo; Zhang, Wencheng; Khan, Musammir; Guo, Jintang

    2013-10-01

    The electrospun scaffolds are potential application in vascular tissue engineering since they can mimic the nano-sized dimension of natural extracellular matrix (ECM). We prepared a fibrous scaffold from polycarbonateurethane (PCU) by electrospinning technology. In order to improve the hydrophilicity and hemocompatibility of the fibrous scaffold, poly(ethylene glycol) methacrylate (PEGMA) was grafted onto the fiber surface by surface-initiated atom transfer radical polymerization (SI-ATRP) method. Although SI-ATRP has been developed and used for surface modification for many years, there are only few studies about the modification of electrospun fiber by this method. The modified fibrous scaffolds were characterized by SEM, Fourier transform infrared (FTIR), and X-ray photoelectron spectroscopy (XPS). The scaffold morphology showed no significant difference when PEGMA was grafted onto the scaffold surface. Based on the water contact angle measurement, the surface hydrophilicity of the scaffold surface was improved significantly after grafting hydrophilic PEGMA (P=0.0012). The modified surface showed effective resistance for platelet adhesion compared with the unmodified surface. Activated partial thromboplastin time (APTT) of the PCU-g-PEGMA scaffold was much longer than that of the unmodified PCU scaffold. The cyto-compatibility of electrospun nanofibrous scaffolds was tested by human umbilical vein endothelial cells (HUVECs). The images of 7-day cultured cells on the scaffold surface were observed by SEM. The modified scaffolds showed high tendency to induce cell adhesion. Moreover, the cells reached out pseudopodia along the fibrous direction and formed a continuous monolayer. Hemolysis test showed that the grafted chains of PEGMA reduced blood coagulation. These results indicated that the modified electrospun nanofibrous scaffolds were potential application as artificial blood vessels.

  19. Surface characteristics of nanocrystalline apatites: effect of mg surface enrichment on morphology, surface hydration species, and cationic environments.

    Science.gov (United States)

    Bertinetti, Luca; Drouet, Christophe; Combes, Christele; Rey, Christian; Tampieri, Anna; Coluccia, Salvatore; Martra, Gianmario

    2009-05-19

    The incorporation of foreign ions, such as Mg2+, exhibiting a biological activity for bone regeneration is presently considered as a promising route for increasing the bioactivity of bone-engineering scaffolds. In this work, the morphology, structure, and surface hydration of biomimetic nanocrystalline apatites were investigated before and after surface exchange with such Mg2+ ions, by combining chemical alterations (ion exchange, H2O-D2O exchanges) and physical examinations (Fourier transform infrared spectroscopy (FTIR) and high-resolution transmission electron microscopy (HRTEM)). HRTEM data suggested that the Mg2+/Ca2+ exchange process did not affect the morphology and surface topology of the apatite nanocrystals significantly, while a new phase, likely a hydrated calcium and/or magnesium phosphate, was formed in small amount for high Mg concentrations. Near-infrared (NIR) and medium-infrared (MIR) spectroscopies indicated that the samples enriched with Mg2+ were found to retain more water at their surface than the Mg-free sample, both at the level of H2O coordinated to cations and adsorbed in the form of multilayers. Additionally, the H-bonding network in defective subsurface layers was also noticeably modified, indicating that the Mg2+/Ca2+ exchange involved was not limited to the surface. This work is intended to widen the present knowledge on Mg-enriched calcium phosphate-based bioactive materials intended for bone repair applications.

  20. Modification of polymeric substrates using surface-grafted nanoscaffolds

    Science.gov (United States)

    Thompson, Kimberlee Fay

    Surface grafting and modification of poly(acrylic acid) (PAA) were performed on nylon 6,6 carpet fibers to achieve permanent stain and soil resistance. PAA was grafted to nylon and modified with 1H, 1H-pentadecafluorooctyl amine (PDFOA) using an amidation agent, 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMTMM). The first goal was to optimize acrylamide modification of PAA in solution. Aqueous reactions with taurine, hydroxyethyl amine, and butyl amine progressed ˜100%, while PDFOA reactions in MeOH progressed ˜80%. Reaction products precipitated at 77% butyl or 52% PDFOA acrylamide contents. The second goal was to optimize the PAA grafting process. First, PAA was adsorbed onto nylon 6,6 films. Next, DMTMM initiated grafting of adsorbed PAA. PAA surface coverage was ˜78%, determined by contact angle analysis of the top 0.1--1 nm and x-ray photoelectron spectroscopy (XPS) analysis of the top 3--10 nm. The third goal was to modify PAA grafted nylon films with butyl amine and PDFOA. Randomly methylated beta-cyclodextrin (RAMEB) solubilized PDFOA in water. Contact angle detected ˜100% surface reaction for each amine, while XPS detected ˜77% butyl amine (H2O) and ˜50% for PDFOA (MeOH or H2O pH = 7) reactions. In H2O pH = 12, the PDFOA reaction progressed ˜89%, perhaps due to greater efficiency, access and solubility. The fourth goal was to perform surface depth profiling via angle-resolved XPS analysis (ARXPS). The PAA surface coverage from contact angle and XPS was confirmed. Further, adsorbed PAA was thicker than grafted PAA, supporting the theory that PAA adsorption occurs in thick layers onto nylon followed by DMTMM-activated spreading and grafting of thinner PAA layers across the surface. The PDFOA reaction in McOH produced a highly fluorinated but thin exterior and an unreacted PAA interior. The PDFOA reaction in H 2O pH = 12 produced a completely fluorinated exterior and highly fluorinated interior. Thus surface modification levels

  1. Surface modification of fluorocarbon polymers by synchrotron radiation

    CERN Document Server

    Kanda, K; Matsui, S; Ideta, T; Ishigaki, H

    2003-01-01

    The surface modification of a poly (tetrafluoroethylene) sheet was carried out by synchrotron radiation in the soft X-ray region. The poly (tetrafluoroethylene) substrate was exposed to synchrotron radiation while varying the substrate temperature from room temperature to 200degC. The contact angle of the modified surfaces with a water drop decreased from 96deg to 72deg by the irradiation at room temperature, while the contact angle increased to 143deg by the irradiation at the substrate temperature of 200degC. Scanning electron microscopy suggested that this repellence was ascribable to the microstructure of the poly (tetrafluoroethylene) surface. We succeeded in controlling the wettability of the poly (tetrafluoroethylene) surface from hydrophobic to hydrophilic by irradiation of the soft X-ray light. (author)

  2. Surface modification and characterization of aramid fibers with hybrid coating

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jianrui; Zhu, Yaofeng; Ni, Qingqing; Fu, Yaqin, E-mail: fyq01@zstu.edu.cn; Fu, Xiang

    2014-12-01

    Graphical abstract: - Highlights: • Aramid fibers modification sizing synthesized by sol–gel in the absence of water. • The strength and interfacial adhesion property of modified fibers were improved. • Modified fibers show a special surface structure. • The mechanism explains the function of structure. - Abstract: Aramid fibers were modified through solution dip-coating and interfacial in situ polymerization using a newly synthesized SiO{sub 2}/shape memory polyurethane (SiO{sub 2}/SMPU) hybrid. Fourier transform infrared and X-ray photoelectron spectroscopy indicated that the synthesized SiO{sub 2}/SMPU hybrid successfully coated the fiber surface. The surface morphology of the aramid fibers and the single fiber tensile strength and interfacial shear strength (IFSS) of the composites were determined. The IFSS of the fiber coated with the hybrid improved by 45%, which benefited from a special “pizza-like” structure on the fiber surface.

  3. Surface modification of PE film by DBD plasma in air

    Energy Technology Data Exchange (ETDEWEB)

    Ren, C.-S. [State Key Laboratory of Material Modification by Electron, Ion and Laser Beams, Dalian University of Technology, Dalian 116023 (China)], E-mail: rchsh@dlut.edu.cn; Wang, K.; Nie, Q.-Y.; Wang, D.-Z.; Guo, S.-H. [State Key Laboratory of Material Modification by Electron, Ion and Laser Beams, Dalian University of Technology, Dalian 116023 (China)

    2008-12-30

    In this paper, surface modification of polyethylene (PE) films is studied by dielectric barrier discharge plasma treatment in air. The treated samples were examined by water contact angle measurement, calculation of surface free energy, Fourier transform infrared attenuated total reflection spectroscopy (FTIR-ATR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The water contact angle changes from the original value of 93.2{sup o} to the minimum value of 53.3{sup o} and surface free energy increases from 27.3 to 51.89 J/m{sup 2} after treatment time of 50 s. Both ATR and XPS show some oxidized species are introduced into the sample surface by the plasma treatment and that the change tendencies of the water contact angle and surface free energy with the treatment time are the same as that of the oxygen concentration on the treated sample surface. Cu films were deposited on the treated and untreated PE surfaces. The peel adhesive strength between the Cu film and the treated sample is 1.5 MPa, whereas the value is only 0.8 MPa between the Cu film and the untreated PE. SEM pictures show that the Cu film deposited on the plasma treated PE surface is smooth and the crystal grain is smaller, contrarily the Cu film on the untreated PE surface is rough and the crystal grain is larger.

  4. Wettability of a quartz surface in the presence of four cationic surfactants.

    Science.gov (United States)

    Zhang, Lei; Wang, Zeng-Lin; Li, Zhen-Quan; Zhang, Lu; Xu, Zhi-Cheng; Zhao, Sui; Yu, Jia-Yong

    2010-12-21

    Advancing contact angle (θ) measurements were carried out for aqueous solutions of four cationic surfactants, hexadecanol glycidyl ether ammonium chloride (C(16)PC), guerbet alcohol hexadecyl glycidyl ether ammonium chloride (C(16)GPC), hexadecanol polyoxyethylene(3) glycidyl ether ammonium chloride (C(16)(EO)(3)PC), and guerbet alcohol hexadecyl polyoxyethylene(3) glycidyl ether ammonium chloride (C(16)G(EO)(3)PC), on the quartz surface using the sessile drop analysis. The influences of surfactant type and bulk concentration on contact angle were expounded, and the changes in adhesional tension and adhesion work were discussed. The contact angle increases up to a maximum with the increasing concentration for all cationic surfactants. Surfactants with branched chain have more hydrophobic group density on the quartz surface, which results in higher values of maxima in contact angle curves. When ethylene oxide groups CH(2)CH(2)O were incorporated in the hydrophobic group, the decrease in contact angle maximum was observed for C(16)(EO)(3)PC and C(16)G(EO)(3)PC. Moreover, an increase in quartz-water interfacial free energy (γ(SL)) has been observed due to the adsorption of four cationic surfactants. The four cationic surfactants can form a monolayer with alignment structure on the quartz surface through electrostatic interaction and then form the bilayer with increasing bulk concentration. In contrast with literature, the maximal contact angles may not necessarily correspond to the beginning of the formation of bilayer for cationic surfactants at the quartz-water interface. Moreover, the concentrations corresponding to maximal contact angles for C(16)PC and C(16)(EO)(3)PC were much lower than their CMC. The contact angle passes through a maximum at a concentration obviously higher than CMC for C(16)G(EO)(3)PC.

  5. The use Na, Li, K cations for modification of ZSM-5 zewolite to control hydrocarbon cold-start emission

    Energy Technology Data Exchange (ETDEWEB)

    Golubeva V.; Rohatgi U.; Korableva, A.; Anischenko, O.; Kustov, L.; Nissenbaum, V; Viola, M.B.

    2012-08-29

    This paper addresses the problem of controlling hydrocarbon emissions from cold-start of engines by investigating the adsorbents which could adsorb the hydrocarbons at cold temperatures and hold them to 250-300 ?. The materials, that has been studied, are based on the modification of ZSM-5 (SiO{sub 2}/Al{sub 2}O{sub 3} = 35) zeolite with Li, K, Na cations. It has been shown that the introduction of Li, Na and K in an amount that is equivalent to the content of Al in zeolite results in occurrence of toluene temperature desorption peaks at high-temperatures. The toluene temperature desorption curves for 5%Li-ZSM-5 and 2.3%Na-ZSM-5 zeolites are identical and have peak toluene desorption rate between 200 to 400 ?. Upon analysis of toluene adsorption isotherms for 2.3%Na-ZSM-5 and 5%Li-ZSM-5, it was concluded that the toluene diffusion inside of the modified zeolites channels is extremely slow and the sorption capacity of 2.3%Na-ZSM-5 is higher than with 5%Li-ZSM-5. The 2.3%Na-ZSM-5 didn't change toluene temperature programmed desorption (TPD) rate of curve after the treatment in environment with 10% ?{sub 2}? at 750-800 ? for about 28 h. The 2.3%Na-ZSM-5 zeolite is very promising as adsorbent to control the cold-start hydrocarbon emissions.

  6. Molecular modeling of organic corrosion inhibitors: why bare metal cations are not appropriate models of oxidized metal surfaces and solvated metal cations.

    Science.gov (United States)

    Kokalj, Anton

    2014-01-01

    The applicability of various models of oxidized metal surfaces - bare metal cations, clusters of various size, and extended (periodic) slabs - that are used in the field of quantum-chemical modeling of corrosion inhibitors is examined and discussed. As representative model systems imidazole inhibitor, MgO surface, and solvated Mg(2+) ion are considered by means of density-functional-theory calculations. Although the results of cluster models are prone to cluster size and shape effects, the clusters of moderate size seem useful at least for qualitative purposes. In contrast, the bare metal cations are useless not only as models of oxidized surfaces but also as models of solvated cations, because they bind molecules several times stronger than the more appropriate models. In particular, bare Mg(2+) binds imidazole by 5.9 eV, while the slab model of MgO(001) by only 0.35 eV. Such binding is even stronger for 3+ cations, e.g., bare Al(3+) binds imidazole by 17.9 eV. The reasons for these fantastically strong binding energies are discussed and it is shown that the strong bonding is predominantly due to electron charge transfer from molecule to metal cation, which stems from differences between molecular and metal ionization potentials.

  7. PREFACE Surface Modifications and Functionalization of Materials for Biomedical Applications

    Science.gov (United States)

    Endrino, Jose Luis; Puértolas, Jose A.; Albella, Jose M.

    2010-11-01

    Conference photograph This special issue contains selected papers which were presented as invited and contributed communications at the workshop entitled 'Surface modification and functionalization of materials for biomedical applications' (BIO-COAT 2010) which was held on 24 June 2010 in Zaragoza (Spain). The surface of a material plays a major role in its interaction with the biological medium. Processes related to the mechanical stability of articular devices in contact, osseointegration, thrombogenicity, corrosion and leaching, or the inflammatory response of rejection of a material, are clearly conditioned by the surface properties. Therefore, the modification or functionalization of surfaces can have an important impact on these issues. New techniques for functionalization by thin film deposition or surface treatments help to improve superficial properties, while understanding the interaction of the surface-biological medium is critical for their application in new devices. Jointly organized by the Spanish Materials Research Society, BIO-COAT 2010 provided an open forum to discuss the progress and latest developments in thin film processing and the engineering of biomaterials. Invited lectures were particularly aimed at providing overviews on scientific topics and were given by recognized world-class scientists. Two of them have contributed with a proceedings article to this selected collection (articles 012001 and 012008). The contributed communications were focused on particular cutting-edge aspects of thin film science and functionalization technologies for biomaterials, showing the major scientific push of Spanish research groups in the field. The 2010 BIO-COAT conference was organized along four main topics: (1) functionalization and texture on surfaces, (2) tribology and corrosion, (3) the surface modification of biomaterials, and (4) surface-biological environment interactions. The papers published in this volume were accepted for publication after

  8. Coatings and surface modifications imparting antimicrobial activity to orthopedic implants.

    Science.gov (United States)

    Kargupta, Roli; Bok, Sangho; Darr, Charles M; Crist, Brett D; Gangopadhyay, Keshab; Gangopadhyay, Shubhra; Sengupta, Shramik

    2014-01-01

    Bacterial colonization and biofilm formation on an orthopedic implant surface is one of the worst possible outcomes of orthopedic intervention in terms of both patient prognosis and healthcare costs. Making the problem even more vexing is the fact that infections are often caused by events beyond the control of the operating surgeon and may manifest weeks to months after the initial surgery. Herein, we review the costs and consequences of implant infection as well as the methods of prevention and management. In particular, we focus on coatings and other forms of implant surface modification in a manner that imparts some antimicrobial benefit to the implant device. Such coatings can be classified generally based on their mode of action: surface adhesion prevention, bactericidal, antimicrobial-eluting, osseointegration promotion, and combinations of the above. Despite several advances in the efficacy of these antimicrobial methods, a remaining major challenge is ensuring retention of the antimicrobial activity over a period of months to years postoperation, an issue that has so far been inadequately addressed. Finally, we provide an overview of additional figures of merit that will determine whether a given antimicrobial surface modification warrants adoption for clinical use.

  9. Surface modification by alkali and heat treatments in titanium alloys.

    Science.gov (United States)

    Lee, Baek-Hee; Do Kim, Young; Shin, Ji Hoon; Hwan Lee, Kyu

    2002-09-01

    Pure titanium and titanium alloys are normally used for orthopedic and dental prostheses. Nevertheless, their chemical, biological, and mechanical properties still can be improved by the development of new preparation technologies. This has been the limiting factor for these metals to show low affinity to living bone. The purpose of this study is to improve the bone-bonding ability between titanium alloys and living bone through a chemically activated process and a thermally activated one. Two kinds of titanium alloys, a newly designed Ti-In-Nb-Ta alloy and a commercially available Ti-6Al-4V ELI alloy, were used in this study. In this study, surface modification of the titanium alloys by alkali and heat treatments (AHT), alkali treated in 5.0M NaOH solution, and heat treated in vacuum furnace at 600 degrees C, is reported. After AHT, the effects of the AHT on the bone integration property were evaluated in vitro. Surface morphologies of AHT were observed by optical microscopy (OM) and scanning electron microscopy (SEM). Chemical compositional surface changes were investigated by X-ray diffractometry (XRD), energy dispersive spectroscopy (EDS), and auger electron spectroscopy (AES). Titanium alloys with surface modification by AHT showed improved bioactive behavior, and the Ti-In-Nb-Ta alloy had better bioactivity than the Ti-6Al-4V ELI alloy in vitro.

  10. Silane surface modification for improved bioadhesion of esophageal stents

    Science.gov (United States)

    Karakoy, Mert; Gultepe, Evin; Pandey, Shivendra; Khashab, Mouen A.; Gracias, David H.

    2014-08-01

    Stent migration occurs in 10-40% of patients who undergo placement of esophageal stents, with higher migration rates seen in those treated for benign esophageal disorders. This remains a major drawback of esophageal stent therapy. In this paper, we propose a new surface modification method to increase the adhesion between self-expandable metallic stents (SEMS) and tissue while preserving their removability. Taking advantage of the well-known affinity between epoxide and amine terminated silane coupling agents with amine and carboxyl groups that are abundant in proteins and related molecules in the human body; we modified the surfaces of silicone coated esophageal SEMS with these adhesive self-assembled monolayers (SAMs). We utilized vapor phase silanization to modify the surfaces of different substrates including PDMS strips and SEMS, and measured the force required to slide these substrates on a tissue piece. Our results suggest that surface modification of esophageal SEMS via covalent attachment of protein-binding coupling agents improves adhesion to tissue and could offer a solution to reduce SEMS migration while preserving their removability.

  11. Surface chemical modification for exceptional wear life of MEMS materials

    Directory of Open Access Journals (Sweden)

    R. Arvind Singh

    2011-12-01

    Full Text Available Micro-Electro-Mechanical-Systems (MEMS are built at micro/nano-scales. At these scales, the interfacial forces are extremely strong. These forces adversely affect the smooth operation and cause wear resulting in the drastic reduction in wear life (useful operating lifetime of actuator-based devices. In this paper, we present a surface chemical modification method that reduces friction and significantly extends the wear life of the two most popular MEMS structural materials namely, silicon and SU-8 polymer. The method includes surface chemical treatment using ethanolamine-sodium phosphate buffer, followed by coating of perfluoropolyether (PFPE nanolubricant on (i silicon coated with SU-8 thin films (500 nm and (ii MEMS process treated SU-8 thick films (50 μm. After the surface chemical modification, it was observed that the steady-state coefficient of friction of the materials reduced by 4 to 5 times and simultaneously their wear durability increased by more than three orders of magnitude (> 1000 times. The significant reduction in the friction coefficients is due to the lubrication effect of PFPE nanolubricant, while the exceptional increase in their wear life is attributed to the bonding between the -OH functional group of ethanolamine treated SU-8 thin/thick films and the -OH functional group of PFPE. The surface chemical modification method acts as a common route to enhance the performance of both silicon and SU-8 polymer. It is time-effective (process time ≤ 11 min, cost-effective and can be readily integrated into MEMS fabrication/assembly processes. It can also work for any kind of structural material from which the miniaturized devices are/can be made.

  12. Surface modification on PMMA : PVDF polyblend: hardening under chemical environment

    Indian Academy of Sciences (India)

    R Bajpai; V Mishra; Pragyesh Agrawal; S C Datt

    2002-02-01

    The influence of chemical environment on polymers include the surface alteration as well as other deep modifications in surface layers. The surface hardening, as an effect of organic liquids on poly(methyl methacrylate): poly(vinylidene fluoride) (PMMA: PVDF), which is one of the few known miscible blends, has been detected using microhardness testing. Organic liquids like acetone, toluene, xylene and benzene were introduced on the surface of blend specimens for different durations. Vickers microhardness (v) was measured for treated and untreated specimens. The study reveals both hardening and plasticization of specimens at different exposure times. The degree of surface hardening is maximum under acetone treatment. All the specimens exhibit surface hardening at an exposure time of 1 h with all the four liquids. This feature is prominent with longer exposures for specimens with increasing content of PVDF. However, the degree of hardening decreases with the time of exposure in the respective environments. In general, acetone and toluene impart surface hardening, whereas, xylene and benzene soften the specimen. PMMA: PVDF (83 : 17) blend exhibits surface hardening under all the four treatments when compared with the respective untreated specimens.

  13. Surface-orientation-dependent distribution of subsurface cation-exchange defects in olivine-phosphate nanocrystals.

    Science.gov (United States)

    Chung, Sung-Yoon; Choi, Si-Young; Kim, Tae-Hwan; Lee, Seongsu

    2015-01-27

    Atomic-scale exchange between two different cations of similar size in crystalline oxides is one of the major types of point defects when multiple cations in oxygen interstitials are arrayed in an ordered manner. Although a number of studies have been performed on a variety of Li-intercalation olivine phosphates to determine the distribution of exchange defects in bulk, understanding of the thermodynamic stability of the defects in subsurface regions and its dependency on the crystallographic orientation at the surface has remained elusive. Through a combination of small-angle neutron scattering, atomic-scale direct probing with scanning transmission electron microscopy, and theoretical ab initio calculations, we directly demonstrate that the antisite exchange defects are distributed in a highly anisotropic manner near the surfaces of LiFePO4 crystals. Moreover, a substantial amount of cation exchanges between Li and Fe sites is identified as an energetically favorable configuration in some surface regions, showing excellent agreement with the calculation results of negative defect formation energies. The findings in this study provide insight into developing better ways to avoid degradation of lithium mobility through the surface as well as scientifically notable features regarding the distribution of exchange defects in olivine phosphates.

  14. Cationic modification and pigment exhaust dyeing of silk fabric%真丝织物阳离子改性及其涂料浸染工艺

    Institute of Scientific and Technical Information of China (English)

    关晋平; 陈国强; 于洋; 张梦甜; 付翰辉

    2012-01-01

    Cationic modification are carried out on silk fabric with cationic modifier S-PD01, and followed by pigment dyeing with pigment pink 118, The parameters of cationic modification and pigment dyeing are discussed. The optimum processes are modification at 70 ℃ for 40 min with S-PD01 7%(omf) and pH value 9-10, and exhaust dyeing at 60 ℃ for 30 min with pigment 6% (omf). The pigment dyeings of silk with cationic modification have obvious improved K/S value compared with those without modification. The color fastness of the dyeings are poor, but can be improved with fixation.%采用阳离子改性剂S-PD01对真丝织物进行阳离子改性处理,然后采用涂料桃红118染色,通过考察真丝阳离子化改性和染色的工艺参数,以优化工艺.优化的真丝改性工艺条件为:阳离子改性剂S-PD017%(omf),pH值9~10,70℃反应40min;涂料染色的优化工艺条件为:涂料6%(omf),60℃染色30min.结果表明,与未经阳离子处理的真丝织物涂料染色试样相比,改性试样染色K/S值显著提高.真丝织物涂料染色的牢度较差,经固色剂处理后有所改善.

  15. Surface modification of glass beads with glutaraldehyde: Characterization and their adsorption property for metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Ozmen, Mustafa; Can, Keziban; Akin, Ilker; Arslan, Gulsin [Department of Chemistry, Selcuk University, 42031, Konya (Turkey); Tor, Ali, E-mail: ali.alitor@gmail.com [Department of Environmental Engineering, Selcuk University, Engineering Faculty, Campus, 42031, Konya (Turkey); Cengeloglu, Yunus; Ersoz, Mustafa [Department of Chemistry, Selcuk University, 42031, Konya (Turkey)

    2009-11-15

    In this study, a new material that adsorbs the metal ions was prepared by modification of the glass beads surfaces with glutaraldehyde. First, the glass beads were etched with 4 M NaOH solution. Then, they were reacted with 3-aminopropyl-triethoxysilane (APTES). Finally, silanized glass beads were treated with 25% of glutaraldehyde solution. The characterization studies by using Fourier Transform Infrared Spectroscopy (FT-IR), Thermal Gravimetric Analysis (TGA), elemental analysis and Scanning Electron Microscopy (SEM) indicated that modification of the glass bead surfaces was successfully performed. The adsorption studies exhibited that the modified glass beads could be efficiently used for the removal of the metal cations and anion (chromate ion) from aqueous solutions via chelation and ion-exchange mechanisms. For both Pb(II) and Cr(VI), selected as model ions, the adsorption equilibrium was achieved in 60 min and adsorption of both ions followed the second-order kinetic model. It was found that the sorption data was better represented by the Freundlich isotherm in comparison to the Langmuir and Redlich-Peterson isotherm models. The maximum adsorption capacities for Pb(II) and Cr(VI) were 9.947 and 11.571 mg/g, respectively. The regeneration studies also showed that modified glass beads could be re-used for the adsorption of Pb(II) and Cr(VI) from aqueous solutions over three cycles.

  16. Fluorescent Magnetic Bioprobes by Surface Modification of Magnetite Nanoparticles

    Directory of Open Access Journals (Sweden)

    Tito Trindade

    2013-07-01

    Full Text Available Bimodal nanoprobes comprising both magnetic and optical functionalities have been prepared via a sequential two-step process. Firstly, magnetite nanoparticles (MNPs with well-defined cubic shape and an average dimension of 80 nm were produced by hydrolysis of iron sulfate and were then surface modified with silica shells by using the sol-gel method. The Fe3O4@SiO2 particles were then functionalized with the fluorophore, fluorescein isothiocyanate (FITC, mediated by assembled shells of the cationic polyelectrolyte, polyethyleneimine (PEI. The Fe3O4 functionalized particles were then preliminary evaluated as fluorescent and magnetic probes by performing studies in which neuroblast cells have been contacted with these nanomaterials.

  17. An Unusual Variation of Surface Tension with Concentration of.Mixed Cationic-anionic Surfactants

    Institute of Scientific and Technical Information of China (English)

    肖进新; 暴艳霞

    2001-01-01

    There are two platforms in the surface tension vs. concentration curve (γ-lgC curve) of cationic-anionic surfactant mixtures. The first platform is the same as that of common surfactant solution, and the cross point is the CMC. After the CMC, the mixtures form precipitate. At higher concentration, the mixtures form homogeneous sloution.When the mixtures form homogeneous solution at high concentration. surface tension increases with concentration, the becomes constant.So the γ-lgC curve exhibits the second platform. The surface tension at the second platform increases by increasing molar ratio of two surfactants and polar group size of surfactants, and decreases with adding inorganic salts.

  18. Surface Organic Modification of Fe3O4 Magnetic Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    CUI Sheng; SHEN Xiaodong; LIN Benlan; JIANG Guodong; ZHANG Weihua

    2008-01-01

    The surface organic modification of Fe3O4 nanoparticles with silane coupling reagent KH570 was studied.The modified and unmodified nanoparticles were characterized by FT-IR,XPS and TEM.The spectra of FT-IR and XPS revealed that KH570 was coated onto the surface of Fe3O4 nanoparticles to get Fe-O-Si bond and an organic coating layer also was formed.Fe3O4 nanoparticles were spheres partly with mean size of 18.8 nm studied by TEM,which was consistent with the result 17.9 nm calculated by Scherrer'S equation.KH570 was adsorbed on surface and formed chemistry bond to be steric hindrance repulsion which prevented nanoparticles from reuniting.Then glycol-based Fe3O4 magnetic liquids dispersed stably was gained.

  19. Surface Modification of SnO2 with Phosphonic Acids

    Directory of Open Access Journals (Sweden)

    Ramona Gheonea

    2017-01-01

    Full Text Available The aim of the present work was the study of phosphonic acids grafting on the surface of SnO2 at different molar ratios. In this paper we describe the functionalization of SnO2 surfaces with phosphonic acids RPO(OH2. The surface modification process was achieved by using phenyl-phosphonic acid (PPA and vinyl-phosphonic acid (VPA. The synthesized materials were investigated by using FT-IR, TGA (in air and in nitrogen, EDX, ESEM, and TEM methods. This synthetic approach has many advantages: films with optical quality and controlled thickness can be obtained using low temperatures and cheap raw materials, by using “green chemistry” synthetic routes. The hybrid materials have structures diversity and fascinating applications, attracting attention for a long time, due to their potential.

  20. Effective modification of particle surface properties using ultrasonic water mist

    DEFF Research Database (Denmark)

    Genina, Natalja; Räikkönen, Heikki; Heinämäki, Jyrki

    2009-01-01

    The goal of the present study was to design a new technique to modify particle surface properties and, through that, to improve flowability of poorly flowing drug thiamine hydrochloride and pharmaceutical sugar lactose monohydrate of two different grades. The powdered particles were supplied...... properties. It was found that rapid exposition of pharmaceutical materials by water mist resulted in the improvement of powder technical properties. The evident changes in flowability of coarser lactose were obviously due to smoothing of particle surface and decreasing in the level of fines with very slight...... increment in particle size. The changes in thiamine powder flow were mainly due to narrowing in particle size distribution where the tendency for better flow of finer lactose was related to surface and size modifications. The aqueous mist application did not cause any alteration of the crystal structures...

  1. [Surface grafting modification and stabilization of Kevlar fiber].

    Science.gov (United States)

    Zheng, Yu-ying; Fu, Ming-lian; Wang, Can-yao; Wang, Liang-en

    2005-11-01

    Chemical disposal was used to bring the activity group onto the surface of Kevlar fiber for the purpose of surface grafting modification. The interfacial constitution of the grafting of toluene-2,4-diisocyanate (TDI) onto Kevlar fiber was determined by Fourier transform infrared spectroscopy. In the mean time, hexyl-lactam stabilization and poly-glycol (400, PEG) stabilization on the grafted product were also studied. The effects of different nTDI:nPEG ratios on the production's interfacial constitution was analysed. It is concluded that the stabilization took place on the surface. The intensity of the bands relented at about 3300 cm(-1) and was reinforced at about 1700-1720 cm(-1) when the ratio of nTDI:nPEG = 1:3, but when the ratio is 1:1 and 1:2, the bands at about 3 300 and 1700-1720 cm(-1) are almost the same.

  2. The study of UHMWPEF surface modification with plasma- induced polymerization

    Science.gov (United States)

    Zhang, Yu-Fang; Jia, Qing-Xiu; Wang, Xin; Zhang, Pei-Ran

    2015-07-01

    In order to improve the surface activity levels of the ultrahigh molecular weight polyethylene fiber (UHMWPEF), as well as enhancing the interface strength of the UHMWPEF based composite materials, the method of plasma-induced polymerization was applied to modify the UHMWPEF surface. In this study, the plasma's power, time, pressure and the grafting monomer concentration were introduced. Also, through a well-conducted comparison and analysis of the grafting rate, fabric surface functional groups and the microcosmic morphology, the most suitable plasma modification process was discovered and determined. The mechanics performance of hybrid composites with the modified UHMWPEF and unidirectional carbon fiber cloth (CF) was tested to reveal that, compared with the unmodified composites, the tensile strength and the laminar shear strength could be improved.

  3. Plasma Processing of Large Curved Surfaces for SRF Cavity Modification

    CERN Document Server

    Upadhyay, J; Popović, S; Valente-Feliciano, A -M; Phillips, L; Vušković, L

    2014-01-01

    Plasma based surface modification of niobium is a promising alternative to wet etching of superconducting radio frequency (SRF) cavities. The development of the technology based on Cl2/Ar plasma etching has to address several crucial parameters which influence the etching rate and surface roughness, and eventually, determine cavity performance. This includes dependence of the process on the frequency of the RF generator, gas pressure, power level, the driven (inner) electrode configuration, and the chlorine concentration in the gas mixture during plasma processing. To demonstrate surface layer removal in the asymmetric non-planar geometry, we are using a simple cylindrical cavity with 8 ports symmetrically distributed over the cylinder. The ports are used for diagnosing the plasma parameters and as holders for the samples to be etched. The etching rate is highly correlated with the shape of the inner electrode, radio-frequency (RF) circuit elements, chlorine concentration in the Cl2/Ar gas mixtures, residence...

  4. Surface modification of ceramic matrix composites induced by laser treatment

    Science.gov (United States)

    Costil, S.; Lukat, S.; Langlade, C.; Coddet, C.

    2008-12-01

    Ceramics or ceramic composites present many advantages (hardness, chemical resistance, low density, etc.) which induce some more and more important applications particularly from the industrial point of view. The evolution of technology can also be beneficial to enlarge their global application areas. This is particularly the aim of this work which consists in applying a laser beam on the ceramic in order to clean its surface. A Nd:YAG laser has been used to study the basic mechanism roughening the surface of silicon carbide composite (ceramic matrix composite (CMC)). Investigations on different surfaces (two chemical compositions) show a strong influence of the nature of the material on the development of a characteristic conic structure. Microscopic studies (SEM) and elementary analyses (EDS and RMS) demonstrated the formation of a regular cone-like structure with a kinetic and a chemical modification specific to each material.

  5. Surface modification of multilayer graphene using Ga ion irradiation

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Quan, E-mail: wangq@mail.ujs.edu.cn [School of Mechanical Engineering, Jiangsu University, Zhenjiang 212013 (China); State Key Laboratory of Transducer Technology, Chinese Academy of Sciences, Shanghai 200050 (China); Shao, Ying; Ge, Daohan; Ren, Naifei [School of Mechanical Engineering, Jiangsu University, Zhenjiang 212013 (China); Yang, Qizhi [School of Mechanical Engineering, Jiangsu University, Zhenjiang 212013 (China); State key laboratory of Robotics, Chinese Academy of Sciences, Shengyang 110000 (China)

    2015-04-28

    The effect of Ga ion irradiation intensity on the surface of multilayer graphene was examined. Using Raman spectroscopy, we determined that the irradiation caused defects in the crystal structure of graphene. The density of defects increased with the increase in dwell times. Furthermore, the strain induced by the irradiation changed the crystallite size and the distance between defects. These defects had the effect of doping the multilayer graphene and increasing its work function. The increase in work function was determined using contact potential difference measurements. The surface morphology of the multilayer graphene changed following irradiation as determined by atomic force microscopy. Additionally, the adhesion between the atomic force microscopy tip and sample increased further indicating that the irradiation had caused surface modification, important for devices that incorporate graphene.

  6. Photochemical surface modification of PET by excimer UV lamp irradiation

    Science.gov (United States)

    Gao, S. L.; Häßler, R.; Mäder, E.; Bahners, T.; Opwis, K.; Schollmeyer, E.

    2005-09-01

    UV irradiation has interesting potential for the photochemical modification of polymers. In order to study cross-linking effects and/or thin-layer deposition following a treatment in the presence of bi-functional media or in inert atmosphere, irradiation of PET in various atmospheres was performed using a KrCl excimer lamp. Surface properties were investigated by atomic force microscopy, nanoindentation, micro-thermal analysis, and X-ray photo-electron spectroscopy. The studies reveal that surface chemical composition, morphology, adhesion, thermomechanics, and stiffness/modulus are strongly affected by UV irradiation in the presence of bi-functional media. Films treated in octadiene and argon show an increase of surface modulus, much less expansion, and lower soft/melt temperatures, which is an indication of the surface cross-linking effect and a decrease of crystallinity within the near-surface layer. In the case of a diallylphthalate-treated film, depending on the local structure, either a strong decrease of melting temperature or no melting point is found, which is attributed to the irregular cross linking and thickness of the modified layer associated with a decrease of surface modulus. A significant increase of the alkali resistance is found after irradiation, as a result of both wetting and cross-linking effects on the polymer surface.

  7. Surface modification of substrates for bacteria and cell culture.

    Science.gov (United States)

    Baede, Tom; Sladek, Raymond; Stoffels, Eva

    2006-10-01

    The plasma needle is a medical device that consists of a tungsten wire placed in a tube through which helium flows. A RF voltage frequency of 13.05 MHz is applied to the wire to produce the plasma. The device has a non-thermal effect and is therefore suited for both organic and inorganic surfaces. It was designed to manipulate tissues, but can also be used to modify the bacterial adhesion properties of material surfaces. The surface modification has a number of applications, most notably cell culture and the preventive treatment of caries. The research consists of two sets of experiments. In the first experiments the effect of the plasma treatment on the wettability was studied by means of contact angle measurements. The wettability quantifies the hydrophilic behavior of a surface. Plasma treatment with the plasma needle significantly increased the wettability of the studied materials. The persistence of the wettability change was also examined. For some materials the effect was only temporary. Bacteria are very particular about the surfaces they adhere to and the wettability of the surface plays an important role in their preference. The next set of experiments dealt with the effect of plasma treatment on bacterial adhesion. This effect was measured by comparing the growth rates of E. coli and S. mutans bacteria that were cultured on both plasma and non-treated surfaces. The effect appears to be species specific.

  8. Surface modification of polycarbonate in homogeneous atmospheric pressure discharge

    Energy Technology Data Exchange (ETDEWEB)

    SIra, M; Trunec, D; St' ahel, P; BursIkova, V; Navratil, Z [Department of Physical Electronics, Faculty of Science, Masaryk University, Kotlarska 2, 611 37 Brno (Czech Republic)

    2008-01-07

    A homogeneous atmospheric pressure dielectric barrier discharge was used for the surface modification of polycarbonate (PC). The discharge was generated between two planar metal electrodes, the top electrode was covered by glass and the bottom electrode was covered by a polymer sample. The discharge burned in pure nitrogen or in a mixture of nitrogen and hydrogen. The surface properties of both treated and untreated polymers were characterized by atomic force microscopy, surface free energy (SFE) measurements and x-ray photoelectron spectroscopy. The influence of the treatment time and power input to the discharge on the surface properties of polymers was studied. The ageing of treated samples was also investigated. The treatment of polymers in the homogeneous atmospheric pressure discharge was homogeneous and the polymer surfaces showed a smaller degree of roughness in comparison with the polymer surfaces treated in a filamentary discharge. The SFE of the treated PC obtained at optimum conditions was 53 mJ m{sup -2} and the corresponding contact angle of water was 38{sup 0}. The maximum decrease in the SFE during ageing was about 13%. The analysis of the chemical composition showed an increase in the nitrogen concentration in the surface layer, but almost a zero increase in the oxygen concentration. This result was discussed concerning the measured values of the SFE measurement.

  9. Microwave absorption by nanoresonator vibrations tuned with surface modification

    Science.gov (United States)

    Krivosudský, Ondrej; Cifra, Michal

    2016-08-01

    Elucidating the physical and chemical parameters that govern viscous damping of nanoresonator vibrations and their coupling to electromagnetic radiation is important for understanding the behavior of matter at the nanoscale. Here we develop an analytical model of microwave absorption of a longitudinally oscillating and electrically polar rod-like nanoresonator embedded in a viscoelastic fluid. We show that the slip length, which can be tuned via surface modifications, controls the quality factor and coupling of nanoresonator vibration modes to microwave radiation. We demonstrate that the larger slip length brings the sharper frequency response of the nanoresonator vibration and electromagnetic absorption. Our findings contribute to design guidelines of fluid embedded nanoresonator devices.

  10. Nonadiabatic nuclear dynamics of the ammonia cation studied by surface hopping classical trajectory calculations

    Science.gov (United States)

    Belyaev, Andrey K.; Domcke, Wolfgang; Lasser, Caroline; Trigila, Giulio

    2015-03-01

    The Landau-Zener (LZ) type classical-trajectory surface-hopping algorithm is applied to the nonadiabatic nuclear dynamics of the ammonia cation after photoionization of the ground-state neutral molecule to the excited states of the cation. The algorithm employs a recently proposed formula for nonadiabatic LZ transition probabilities derived from the adiabatic potential energy surfaces. The evolution of the populations of the ground state and the two lowest excited adiabatic states is calculated up to 200 fs. The results agree well with quantum simulations available for the first 100 fs based on the same potential energy surfaces. Three different time scales are detected for the nuclear dynamics: Ultrafast Jahn-Teller dynamics between the excited states on a 5 fs time scale; fast transitions between the excited state and the ground state within a time scale of 20 fs; and relatively slow partial conversion of a first-excited-state population to the ground state within a time scale of 100 fs. Beyond 100 fs, the adiabatic electronic populations are nearly constant due to a dynamic equilibrium between the three states. The ultrafast nonradiative decay of the excited-state populations provides a qualitative explanation of the experimental evidence that the ammonia cation is nonfluorescent.

  11. Multifunctional Indium Tin Oxide Electrode Generated by Unusual Surface Modification

    Science.gov (United States)

    Bouden, Sarra; Dahi, Antoine; Hauquier, Fanny; Randriamahazaka, Hyacinthe; Ghilane, Jalal

    2016-11-01

    The indium tin oxide (ITO) material has been widely used in various scientific fields and has been successfully implemented in several devices. Herein, the electrochemical reduction of ITO electrode in an organic electrolytic solution containing alkali metal, NaI, or redox molecule, N-(ferrocenylmethyl) imidazolium iodide, was investigated. The reduced ITO surfaces were investigated by X-ray photoelectron spectroscopy and grazing incident XRD demonstrating the presence of the electrolyte cation inside the material. Reversibility of this process after re-oxidation was evidenced by XPS. Using a redox molecule based ionic liquid as supporting electrolyte leads to fellow electrochemically the intercalation process. As a result, modified ITO containing ferrocenyl imidazolium was easily generated. This reduction process occurs at mild reducing potential around -1.8 V and causes for higher reducing potential a drastic morphological change accompanied with a decrease of the electrode conductivity at the macroscopic scale. Finally, the self-reducing power of the reduced ITO phase was used to initiate the spontaneous reduction of silver ions leading to the growth of Ag nanoparticles. As a result, transparent and multifunctional active ITO surfaces were generated bearing redox active molecules inside the material and Ag nanoparticles onto the surface.

  12. Preparation of bactericidal cationic PDMS surfaces using a facile and efficient approach

    Science.gov (United States)

    Kébir, Nasreddine; Kriegel, Irène; Estève, Marc; Semetey, Vincent

    2016-01-01

    Two cationic polymers containing vinyl and quaternary ammonium groups were successfully grafted on silicone surfaces containing Sisbnd H groups. The reaction was carried out by straightforward hydrosilylation reaction in water without using exogenous catalyst and without doping the surface with Sisbnd H groups. The Sisbnd H content was varied by changing the curing time or the ratio between silicone components. The surfaces obtained exhibited quaternary ammonium densities ranging from 1.8 ÿ 1014 to 2.8 ÿ 1015 charge/cm2 and higher polarity and hydrophilicity in comparison with non grafted surfaces. Bactericidal effects of these surfaces against Escherichia coli and Staphylococcus epidermidis were evidenced. This study have evidenced also the fouling of the poly(quaternary ammonium) (PQA) surfaces by contact with plasmatic proteins probably limiting their use in some biomedical field (e.g. implantable medical devices).

  13. Surface Modification on Acoustic Wave Biosensors for Enhanced Specificity

    Directory of Open Access Journals (Sweden)

    Nathan D. Gallant

    2012-09-01

    Full Text Available Changes in mass loading on the surface of acoustic biosensors result in output frequency shifts which provide precise measurements of analytes. Therefore, to detect a particular biomarker, the sensor delay path must be judiciously designed to maximize sensitivity and specificity. B-cell lymphoma 2 protein (Bcl-2 found in urine is under investigation as a biomarker for non-invasive early detection of ovarian cancer. In this study, surface chemistry and biofunctionalization approaches were evaluated for their effectiveness in presenting antibodies for Bcl-2 capture while minimizing non-specific protein adsorption. The optimal combination of sequentially adsorbing protein A/G, anti-Bcl-2 IgG and Pluronic F127 onto a hydrophobic surface provided the greatest signal-to-noise ratio and enabled the reliable detection of Bcl-2 concentrations below that previously identified for early stage ovarian cancer as characterized by a modified ELISA method. Finally, the optimal surface modification was applied to a prototype acoustic device and the frequency shift for a range of Bcl-2 concentration was quantified to demonstrate the effectiveness in surface acoustic wave (SAW-based detection applications. The surface functionalization approaches demonstrated here to specifically and sensitively detect Bcl-2 in a working ultrasonic MEMS biosensor prototype can easily be modified to detect additional biomarkers and enhance other acoustic biosensors.

  14. Development of Methods for Surface Modification of Nanostructured Materials

    Science.gov (United States)

    Marsh, David A.

    The surfaces of a material become increasingly more influential when the dimensions are reduced, because a larger percentage of the atoms are exposed on the surface. The surface environment of nanostructured materials dictates both physical properties and function, but is synthetically challenging to control. Although the desired functionality is commonly introduced via post-synthetic modification, it would be advantageous to minimize the number of synthetic steps by having specific function installed in the precursor. This work describes efforts to investigate new precursor complexes for the synthesis of nanoparticles, in addition to electrochemical studies on single monolayer films for electrocatalysis. Chapter 2 focuses on the preparation of magnetic nanoaparticles, and the synthesis of a polymerizable surfactant, stacac, to be used to generate composite materials. Although an iron complex of stacac could be used as a precursor for magnetic nanoparticles, favorable composite materials could only be produced by introduction of stacac after isolation of magnetic nanoparticles. Chapter 3 describes the synthesis of Au(I) complexes with various thiourea-based ligands, to be used as precursors for gold nanoparticles. The experimental conditions were varied and parameters were found where addition of a reducing agent generated solution-stable gold nanoparticles in a reproducible manner. It was determined that only aggregated gold nanoparticles were produced when Au(I) complexes were generated in situ and the use of crystalline precursors resulted in soluble gold nanoparticles. Chapter 4 discusses the preparation of electrocatalysts for the oxidation of water with a focus on accurately determining the active surface area. A monolayer of cobalt was prepared on a gold electrode by underpotential deposition and used as an electrocatalyst for water oxidation. Because the surface area of gold can be measured directly, deposition of a single monolayer produced negligible

  15. Surface assessment and modification of concrete using abrasive blasting

    Science.gov (United States)

    Millman, Lauren R.

    Composite systems are applied to concrete substrates to strengthen and extend the service life. Successful restoration or rehabilitation requires surface preparation prior to the application of the overlay. Surface coatings, waterproofing systems, and other external surface applications also require surface preparation prior to application. Abrasive blast media is often used to clean and uniformly roughen the substrate. The appropriate surface roughness is necessary to facilitate a strong bond between the existing substrate and overlay. Thus, surface modification using abrasive blast media (sand and dry ice), their respective environmental effects, surface roughness characterization prior to and after blasting, and the adhesion between the substrate and overlay are the focus of this dissertation. This dissertation is comprised of an introduction, a literature review, and four chapters, the first of which addresses the environmental effects due to abrasive blasting using sand, water, and dry ice. The assessment considered four response variables: carbon dioxide (CO2) emissions, fuel and energy consumption, and project duration. The results indicated that for sand blasting and water jetting, the primary factor contributing to environmental detriment was CO22 emissions from vehicular traffic near the construction site. The second chapter is an analysis of the International Concrete Repair Institute's (ICRI) concrete surface profiles (CSPs) using 3-D optical profilometry. The primary objective was to evaluate the suitability of approximating the 3-D surface (areal) parameters with those extracted from 2-D (linear) profiles. Four profile directions were considered: two diagonals, and lines parallel and transverse to the longitudinal direction of the mold. For any CSP mold, the estimation of the 3-D surface roughness using a 2-D linear profile resulted in underestimation and overestimation errors exceeding 50%, demonstrating the inadequacy of 2-D linear profiles to

  16. Surface functionalized SiO2 nanoparticles with cationic polymers via the combination of mussel inspired chemistry and surface initiated atom transfer radical polymerization: Characterization and enhanced removal of organic dye.

    Science.gov (United States)

    Huang, Qiang; Liu, Meiying; Mao, Liucheng; Xu, Dazhuang; Zeng, Guangjian; Huang, Hongye; Jiang, Ruming; Deng, Fengjie; Zhang, Xiaoyong; Wei, Yen

    2017-03-28

    Monodispersed SiO2 particles functionalized with cationic polymers poly-((3-acrylamidopropyl)trimethylammonium chloride) (PAPTCl) were prepared using mussel inspired surface modification strategy and surface initiated atom transfer radical polymerization (SI-ATRP). Fourier transform infrared spectroscopy, transmission electron microscope, thermogravimetric analysis, X-ray photoelectron spectroscopy, and zeta potential were employed to characterize these SiO2 samples. The adsorption performance of the functionalized SiO2 (donated as SiO2-PDA-PAPTCl) towards anionic organic dye Congo red (CR) was investigated to evaluate their potential environmental applications. We demonstrated that the surface of SiO2 particles can be successfully functionalized with cationic PAPTCl. The adsorption capability of as-prepared SiO2 was found to increases from 28.70 and 106.65mg/g after surface grafted with cationic polymers. The significant enhancement in the adsorption capability of SiO2-PDA-PAPTCl is mainly attributed to the introduction of cationic polymers. More importantly, this strategy is expected to be promising for fabrication of many other functional polymer nanocomposites for environmental applications due to the universality of mussel inspired chemistry and well designability and good monomer adaptability of SI-ATRP.

  17. Surface Modification of Medical Polyurethane by Plasma Treatment

    Science.gov (United States)

    Li, Dejun; Zhao, Jie; Gu, Hanqing; Lu, Mozhu; Ding, Fuqing; Hu, Jianfang

    1992-02-01

    The wettability and surface structure of plasma treatment on medical polyurethane were studied. Two kinds of gas, N2, Ar, were used to create the low-temperature plasma under low pressure. The wettability was investigated by means of the sessile drop method using water, the results show that the contact angle of water decreases from 78.8° to 61.9° as the treatment time increases. The results of electron spectroscopy for chemical analysis indicate that original chemical bonds were broken up after plasma treatment, which was the main reason for the surface modification. At same time, the results of electron spinning resonance show that the amounts of radicals did not increase significantly after treatment, which is advantageous to clinical practice of polyurethane.

  18. Surface Modification of Biomaterials in Hard Tissue Applications

    Institute of Scientific and Technical Information of China (English)

    LIU Xuan-yong; DING Chuan-xian; CHU Paul K

    2004-01-01

    Surface modification technologies are quite common in the biomedical field to improve the mechanical,chemical, physical and biological properties of implants such as artificial joint and cardiovascular devices. In this paper, recent progress in the investigation of the bioactivity and biocompatibility enhancement of implants using plasma spraying and plasmabased ion implantation (PIII) is described. Plasma sprayed hydroxyapatite (HA) coatings are commonly used as bioactive coatings but the relatively poor adhesion between the coatings and titanium is one of main disadvantages which have limited their biomedical applications. In our recent studies, novel bioactive coatings, such as wollastonite and dicalcium silicate, were deposited onto titanium to enhance the surfaces bioactivity and biocompatibility. Our results indicate that plasma sprayed wollastonite and dicalcium silicate coatings possess excellent bioactivity as well as relatively high bonding strength. Plasma immersion ion implantation was also employed to improve the anti-corrosion and biological properties of implants.

  19. Atmospheric Microplasma Application for Surface Modification of Biomaterials

    Science.gov (United States)

    Shimizu, Kazuo; Fukunaga, Hodaka; Tatematsu, Shigeki; Blajan, Marius

    2012-11-01

    Atmospheric microplasma has been intensively studied for applications in various fields, since in this technology the generated field is only 1 kV (approx) under atmospheric pressure and a dielectric barrier discharge gap of 10 to 100 µm. A low discharge voltage atmospheric plasma process is an economical and effective solution for various applications such as indoor air control including sterilization, odor removal, and surface treatment, and would be suitable for medical applications in the field of plasma life sciences. In this paper, we present the application of microplasma for the surface treatment of materials used in medical fields. Moreover, a biomaterial composed of L-lactic acid is used in experiments, which can be biodecomposed in the human body after medical operations. The surface modification process was carried out with active species generated between the microplasma electrodes, which were observed by emission spectrometry. Microplasma treatment of a polymer sheet using Ar as the process gas decreased the contact angle of a water droplet at the surface of the polymer from 78.3 to 45.6° in 10 s, indicating improved surface adhesive characteristics.

  20. Surface modification of piezoelectric aluminum nitride with functionalizable organosilane adlayers

    Science.gov (United States)

    Chan, Edmund; Jackson, Nathan; Mathewson, Alan; Galvin, Paul; Alamin Dow, Ali B.; Kherani, Nazir P.; Blaszykowski, Christophe; Thompson, Michael

    2013-10-01

    The world of biosensors is expanding at a rapid pace with an ever-increasing demand for more sensitive miniaturized devices. Acoustic wave biosensors are not spared from this trend. In this domain, the search for enhanced sensitivity is increasingly oriented toward the rational design of new piezoelectric materials with superior properties to substitute for prevalent quartz. With respect to surface chemistry, construction of the biorecognition element, more often than not, requires the use of bifunctional molecules that can spontaneously assemble on the substrate and form organic surfaces readily biofunctionalizable in a subsequent, ideally single step. In this context, we present herein the surface modification of aluminum nitride (AlN) with alkyltrichlorosilane cross-linking molecules bearing a functionalizable benzenethiosulfonate moiety. This latter feature is next demonstrated through the straightforward, preactivation-free immobilization of thiolated biotin probes. To date, AlN has only received little attention in the field of piezoelectric biosensors despite its many attractive properties and the perspective to operate devices at ultra-high frequencies (GHz) with unprecedented sensitivity. To our knowledge, this work describes one of the first examples of direct surface derivatization of AlN with bifunctional trichlorosilane molecules. It also constitutes a first step toward the development of electrodeless GHz piezoelectric biosensing platforms based on AlN and trichlorosilane surface chemistry.

  1. Green aqueous surface modification of polypropylene for novel polymer nanocomposites.

    Science.gov (United States)

    Thakur, Vijay Kumar; Vennerberg, Danny; Kessler, Michael R

    2014-06-25

    Polypropylene is one of the most widely used commercial commodity polymers; among many other applications, it is used for electronic and structural applications. Despite its commercial importance, the hydrophobic nature of polypropylene limits its successful application in some fields, in particular for the preparation of polymer nanocomposites. Here, a facile, plasma-assisted, biomimetic, environmentally friendly method was developed to enhance the interfacial interactions in polymer nanocomposites by modifying the surface of polypropylene. Plasma treated polypropylene was surface-modified with polydopamine (PDA) in an aqueous medium without employing other chemicals. The surface modification strategy used here was based on the easy self-polymerization and strong adhesion characteristics of dopamine (DA) under ambient laboratory conditions. The changes in surface characteristics of polypropylene were investigated using FTIR, TGA, and Raman spectroscopy. Subsequently, the surface modified polypropylene was used as the matrix to prepare SiO2-reinforced polymer nanocomposites. These nanocomposites demonstrated superior properties compared to nanocomposites prepared using pristine polypropylene. This simple, environmentally friendly, green method of modifying polypropylene indicated that polydopamine-functionalized polypropylene is a promising material for various high-performance applications.

  2. Cationic poly(ɛ-caprolactone) surface functionalized mesoporous silica nanoparticles and their application in drug delivery

    Science.gov (United States)

    Zhang, Yan; Wang, Zhaojun; Zhou, Weimin; Min, Guoquan; Lang, Meidong

    2013-07-01

    Cationic poly(ɛ-caprolactone) modified hollow mesoporous silica (HMSNs) was achieved by a post graft method via covalent linkage between the silanols on the surface of silica and the trimethoxysilane groups at the end of the poly(γ-(carbamic acid benzyl ester)-ɛ-caprolactone). The trimethoxysilane groups were introduced to poly(γ-(carbamic acid benzyl ester)-ɛ-caprolactone) by ring opening polymerization of γ-(carbamic acid benzyl ester)-ɛ-caprolactone (γCABɛCL) with 3-aminopropyl trimethoxysilane as initiator. Subsequently, the polymer was grafted to the HMSNs and the protected groups of Cbz were removed, thus the amino groups were obtained accordingly. The structure of the polymer was confirmed by 1H NMR. In addition, the TEM and SEM demonstrated that the HMSNs were spherical and the polymer was well coated on the spheres. FTIR, TGA and N2 adsorption results proved that the modified processes were effective and the structure of the HMSNs was well reserved. The cationic surface was further confirmed by zeta potential. Moreover, the potential application of the HMSNs in drug delivery was studied with ammonium glycyrrhizinate (AMG) as model drug. Results showed that the cationic HMSNs could be an efficient AMG carrier.

  3. Modeling the Interaction between Integrin-Binding Peptide (RGD) and Rutile Surface: The Effect of Cation Mediation on Asp Adsorption

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Chunya [Harbin Institute of Technology; Skelton, Adam [Vanderbilt University; Chen, Mingjun [Harbin Institute of Technology; Vlcek, Lukas [ORNL; Cummings, Peter T [ORNL

    2012-01-01

    The binding of a negatively charged residue, aspartic acid (Asp) in tripeptide arginine-glycine-aspartic acid, onto a negatively charged hydroxylated rutile (110) surface in aqueous solution, containing divalent (Mg{sup 2+}, Ca{sup 2+}, or Sr{sup 2+}) or monovalent (Na{sup +}, K{sup +}, or Rb{sup +}) cations, was studied by molecular dynamics (MD) simulations. The results indicate that ionic radii and charges will significantly affect the hydration, adsorption geometry, and distance of cations from the rutile surface, thereby regulating the Asp/rutile binding mode. The adsorption strength of monovalent cations on the rutile surface in the order Na{sup +} > K{sup +} > Rb{sup +} shows a 'reverse' lyotropic trend, while the divalent cations on the same surface exhibit a 'regular' lyotropic behavior with decreasing crystallographic radii (the adsorption strength of divalent cations: Sr{sup 2+} > Ca{sup 2+} > Mg{sup 2+}). The Asp side chain in NaCl, KCl, and RbCl solutions remains stably H-bonded to the surface hydroxyls and the inner-sphere adsorbed compensating monovalent cations act as a bridge between the COO{sup -} group and the rutile, helping to 'trap' the negatively charged Asp side chain on the negatively charged surface. In contrast, the mediating divalent cations actively participate in linking the COO{sup -} group to the rutile surface; thus the Asp side chain can remain stably on the rutile (110) surface, even if it is not involved in any hydrogen bonds with the surface hydroxyls. Inner- and outer-sphere geometries are all possible mediation modes for divalent cations in bridging the peptide to the rutile surface.

  4. Cationic schiff base amphiphiles and their metal complexes: Surface and biocidal activities against bacteria and fungi.

    Science.gov (United States)

    Negm, N A; Zaki, M F; Salem, M A I

    2010-05-01

    A series of cationic surfactants containing schiff base groups was synthesized by condensation of four fatty amines namely: dodecyl, tetradecyl, hexadecyl and octadecyl amine and 4-diethyl aminobenzaldehyde (1-4), as well as their metal complexes with divalent transition metal ions including Co, Cu and Mn (5-16). The surface activities of the synthesized surfactants were influenced by their chemical structures and the type of the transition metals. The biological activity measurements of the parent cationic schiff bases showed high efficacy against Gram positive and Gram negative bacterial strains and fungi. While on complexation, the biocidal activity was increased remarkably. The biocidal activity of the tested compounds against sulfur reducing bacteria showed promising results in the field of biocide applications.

  5. Arsenic and major cation hydrogeochemistry of the Central Victorian (Australia) surface waters

    Institute of Scientific and Technical Information of China (English)

    Khawar SULTAN; Kim DOWLING

    2006-01-01

    This paper reports on the major cations(Ca, Mg, Na and K) and arsenic(As) compositions of surface waters collected from major creeks, rivers and lakes in Central Victoria (Australia). The surface waters were found to be neutral to alkaline (pH 6.7-9.4),oxidised (average redox potential (Eh) about 130 mV) and showed variable concentrations of dissolved ions (EC, about 51-4386 μS/cm). The concen- trations of dissolved major cations in surface waters were found to be in the order of Na>>Mg>Ca>K and in soils the contents of metals followed an order of abundance as: Ca>Mg>>K>Na. While Na was the least abundant in soils, it registered the highest dissolved cation in surface waters. Of the four major cations, the average concentration ofNa(98.7 mg/L) was attributed to the weathering of feldspars and atmospheric input. Relatively highly dissolved concentrations of Na and Mg compared with the world average values of rivers reflected the weathering of rock and soil minerals within the catchments.The As soil level is naturally high(linked to lithology) as reflected by high background soil values and mining operations are also considered to be a contributory factor. Under relatively alkaline-oxidative conditions low mobility of dissolved As (average about 7.9 μg/L) was observed in most of the surface waters with a few higher values(>15 μg/L) around a sewage disposal site and mine tailings.Arsenic in soils is slowly released into water under alkaline and/or lower Eh conditions. The efficient sink of Fe, Al and Mn oxides acts as a barrier against the As release under near neutral-oxidising conditions. High As content (average about 28.3 mg/kg) in soils was found to be associated with Fe-hydroxides as revealed by XRD and SEM analysis. The dissolved As concentration was found to be below the recommended maximum levels for recreational water in all surface waters(lakes and rivers) in the study area. Catchment lithology exerted the fundamental control on surface water chemistry

  6. Surface modification of closed plastic bags for adherent cell cultivation

    Science.gov (United States)

    Lachmann, K.; Dohse, A.; Thomas, M.; Pohl, S.; Meyring, W.; Dittmar, K. E. J.; Lindenmeier, W.; Klages, C.-P.

    2011-07-01

    In modern medicine human mesenchymal stem cells are becoming increasingly important. However, a successful cultivation of this type of cells is only possible under very specific conditions. Of great importance, for instance, are the absence of contaminants such as foreign microbiological organisms, i.e., sterility, and the chemical functionalization of the ground on which the cells are grown. As cultivation of these cells makes high demands, a new procedure for cell cultivation has been developed in which closed plastic bags are used. For adherent cell growth chemical functional groups have to be introduced on the inner surface of the plastic bag. This can be achieved by a new, atmospheric-pressure plasma-based method presented in this paper. The method which was developed jointly by the Fraunhofer IST and the Helmholtz HZI can be implemented in automated equipment as is also shown in this contribution. Plasma process gases used include helium or helium-based gas mixtures (He + N2 + H2) and vapors of suitable film-forming agents or precursors such as APTMS, DACH, and TMOS in helium. The effect of plasma treatment is investigated by FTIR-ATR spectroscopy as well as surface tension determination based on contact angle measurements and XPS. Plasma treatment in nominally pure helium increases the surface tension of the polymer foil due to the presence of oxygen traces in the gas and oxygen diffusing through the gas-permeable foil, respectively, reacting with surface radical centers formed during contact with the discharge. Primary amino groups are obtained on the inner surface by treatment in mixtures with nitrogen and hydrogen albeit their amount is comparably small due to diffusion of oxygen through the gas-permeable bag, interfering with the plasma-amination process. Surface modifications introducing amino groups on the inner surface turned out to be most efficient in the promotion of cell growth.

  7. MODIFICATION OF SURFACE LAYERS FOR SILICATE GLASSES BY ELECTRON IRRADIATION

    Directory of Open Access Journals (Sweden)

    V. S. Brunov

    2014-05-01

    Full Text Available Experimental research results of silicate glass surface layers modification by the influence of electron beams with 5-50 keV energies and 20-50 mC/cm2 doses are presented. It is shown that during the glasses exposure to an electron beam with 20-50 keV electron energies, a gradient optical waveguide with increased refractive index on waveguide axis Δn = 0.01-0.04 is formed in the surface layer. Сhemical etching rate is increased in the exposed area by up to two times which is related to glass grid destruction. Depending on irradiation dose thin film or silver nanoparticles with the size less than 20nm are formed on the surface of the silver containing glasses for electron energies less than 10 keV. Silver films drawn on the surface of the glass are dissolved into the glass bulk for electron energies 20-50 keV and 20-50 mC/cm2 dose. Basic mechanisms causing these effects are: chemical bonds breaking of spatial glass grid by high energy electrons, formation of negative volume charge inside the glass and field migration of positive metal ions into the volume charge region. Achieved results can be used in photonics, integral optics and nanoplasmonics device fabrication.

  8. Surface modification of multiwall carbon nanotubes by sulfonitric treatment

    Science.gov (United States)

    Gómez, Sofía; Rendtorff, Nicolás M.; Aglietti, Esteban F.; Sakka, Yoshio; Suárez, Gustavo

    2016-08-01

    Carbon nanotubes are widely used for electronic, mechanical, and optical devices due to their unique structural and quantum characteristics. The species generated by oxidation on the surface of these materials permit binding new reaction chains, which improves the dispersibility, processing and compatibility with other materials. Even though different acid treatments and applications of these CNT have been reported, relatively few research studies have focused on the relationship between the acid treatment and the formation of nanodefects, specific oxidized species or CNT surface defects. In this work, multiwall carbon nanotube (MWCNT) oxidation at 90 °C was characterized in order to determine the acid treatment effect on the surface. It was found that oxidized species are already present in MWCNT without an acid treatment, but there are not enough to cause water-based dispersion. The species were identified and quantified by infrared spectroscopy and X-ray photoelectron spectroscopy. Also, transmission electron microscopy observations showed not only modifications of the oxidized species, but also morphological damage on the surfaces of MWCNT after being subjected to the acid treatment. This effect was also confirmed by Raman spectroscopy. The acid treatment generates higher oxidized species, decreasing the zeta potential in the whole pH range.

  9. Nanoscale Surface Modification of Lithium-Rich Layered-Oxide Composite Cathodes for Suppressing Voltage Fade.

    Science.gov (United States)

    Zheng, Fenghua; Yang, Chenghao; Xiong, Xunhui; Xiong, Jiawen; Hu, Renzong; Chen, Yu; Liu, Meilin

    2015-10-26

    Lithium-rich layered oxides are promising cathode materials for lithium-ion batteries and exhibit a high reversible capacity exceeding 250 mAh g(-1) . However, voltage fade is the major problem that needs to be overcome before they can find practical applications. Here, Li1.2 Mn0.54 Ni0.13 Co0.13 O2 (LLMO) oxides are subjected to nanoscale LiFePO4 (LFP) surface modification. The resulting materials combine the advantages of both bulk doping and surface coating as the LLMO crystal structure is stabilized through cationic doping, and the LLMO cathode materials are protected from corrosion induced by organic electrolytes. An LLMO cathode modified with 5 wt % LFP (LLMO-LFP5) demonstrated suppressed voltage fade and a discharge capacity of 282.8 mAh g(-1) at 0.1 C with a capacity retention of 98.1 % after 120 cycles. Moreover, the nanoscale LFP layers incorporated into the LLMO surfaces can effectively maintain the lithium-ion and charge transport channels, and the LLMO-LFP5 cathode demonstrated an excellent rate capacity.

  10. Surface modification of multiwall carbon nanotubes by sulfonitric treatment

    Energy Technology Data Exchange (ETDEWEB)

    Gómez, Sofía, E-mail: sofiagomez@cetmic.unlp.edu.ar [Centro de Tecnología de Recursos Minerales y Cerámica (CETMIC), Camino Centenario y 506, C.C.49, M.B. Gonnet B1897ZCA (Argentina); Rendtorff, Nicolás M., E-mail: rendtorff@cetmic.unlp.edu.ar [Centro de Tecnología de Recursos Minerales y Cerámica (CETMIC), Camino Centenario y 506, C.C.49, M.B. Gonnet B1897ZCA (Argentina); Departamento de Química, Facultad de Ciencias Exactas—UNLP, Calle 115 y 47, La Plata 1900 (Argentina); Aglietti, Esteban F., E-mail: eaglietti@cetmic.unlp.edu.ar [Centro de Tecnología de Recursos Minerales y Cerámica (CETMIC), Camino Centenario y 506, C.C.49, M.B. Gonnet B1897ZCA (Argentina); Departamento de Química, Facultad de Ciencias Exactas—UNLP, Calle 115 y 47, La Plata 1900 (Argentina); Sakka, Yoshio, E-mail: SAKKA.Yoshio@nims.go.jp [National Institute for Materials Science, Tsukuba, Ibaraki 305-0047 (Japan); Suárez, Gustavo, E-mail: gsuarez@cetmic.unlp.edu.ar [Centro de Tecnología de Recursos Minerales y Cerámica (CETMIC), Camino Centenario y 506, C.C.49, M.B. Gonnet B1897ZCA (Argentina); Departamento de Química, Facultad de Ciencias Exactas—UNLP, Calle 115 y 47, La Plata 1900 (Argentina)

    2016-08-30

    Highlights: • After the acid treatment highly increase the amount carbonyl and carboxylic groups. • The oxidation of MWCNT generates a high negative charge of it in all the pH range. • It could achieve a good dispersion of the MWCNT in water-based suspension. • There is morphological damage on the surfaces of MWCNT after the acid treatment. • Some surface defects but no shortening were observed by TEM images. - Abstract: Carbon nanotubes are widely used for electronic, mechanical, and optical devices due to their unique structural and quantum characteristics. The species generated by oxidation on the surface of these materials permit binding new reaction chains, which improves the dispersibility, processing and compatibility with other materials. Even though different acid treatments and applications of these CNT have been reported, relatively few research studies have focused on the relationship between the acid treatment and the formation of nanodefects, specific oxidized species or CNT surface defects. In this work, multiwall carbon nanotube (MWCNT) oxidation at 90 °C was characterized in order to determine the acid treatment effect on the surface. It was found that oxidized species are already present in MWCNT without an acid treatment, but there are not enough to cause water-based dispersion. The species were identified and quantified by infrared spectroscopy and X-ray photoelectron spectroscopy. Also, transmission electron microscopy observations showed not only modifications of the oxidized species, but also morphological damage on the surfaces of MWCNT after being subjected to the acid treatment. This effect was also confirmed by Raman spectroscopy. The acid treatment generates higher oxidized species, decreasing the zeta potential in the whole pH range.

  11. A bioinspired strategy for surface modification of silica nanoparticles

    Science.gov (United States)

    Tian, Jianwen; Zhang, Haoxuan; Liu, Meiying; Deng, Fengjie; Huang, Hongye; Wan, Qing; Li, Zhen; Wang, Ke; He, Xiaohui; Zhang, Xiaoyong; Wei, Yen

    2015-12-01

    Silica nanoparticles have become one of the most promising nanomaterials for a vast of applications. In this work, a novel strategy for surface modification of silica nanoparticles has been developed for the first time via combination of mussel inspired chemistry and Michael addition reaction. In this procedure, thin polydopamine (PDA) films were first coated on the bare silica nanoparticles via self-polymerization of dopamine in alkaline condition. And then amino-containing polymers were introduced onto the PDA coated silica nanoparticles through Michael addition reaction, that are synthesized from free radical polymerization using poly(ethylene glycol) methyl methacrylate (PEGMA) and N-(3-aminopropyl) methacrylamide (NAPAM) as monomers and ammonium persulfate as the initiator. The successful modification of silica nanoparticles was evidenced by a series of characterization techniques. As compared with the bare silica nanoparticles, the polymers modified silica nanoparticles showed remarkable enhanced dispersibility in both aqueous and organic solution. This strategy is rather simple, effective and versatile. Therefore, it should be of specific importance for further applications of silica nanoparticles and will spark great research attention of scientists from different fields.

  12. The influence of clay surface modification with berberine on the sorption of anthocyanins

    Science.gov (United States)

    Chulkov, A. N.; Deineka, V. I.; Tikhova, A. A.; Vesentzev, A. I.; Deineka, L. A.

    2012-03-01

    The influence of preliminary sorption of berberine on the sorption of anthocyanins by bentonite clay was studied. The cation exchange sorption mechanism was found to be replaced by hydrophobic sorption of these compounds after clay modification with berberine. The enthalpy of sorption along the initial isotherm part changed from endothermic to exothermic.

  13. CHEMICAL MODIFICATION OF THE SURFACE OF CALCIUM ALGINATE GEL BEADS

    Institute of Scientific and Technical Information of China (English)

    Cong-ming Xiao; Li-chun Zhou

    2004-01-01

    The chemical modification of the surface of calcium alginate gel beads (CAGB) via grafting copolymerization with vinyl acetate (VAc) was studied. The optimum reaction conditions with activation and graft copolymerization two steps were explored. First, 5 grams CAGB with 2.5 mm initial diameter was initiated with 0.0493 mol/L K2S2O8 at 51 ℃ for 30 min in 15 mL 1% PVA/H2O. Then 4.34 mol/L VAc was added dropwise and the reaction was allowed to proce at 48 ℃ for 3 h. The grafting efficiency could come up to 30%. It was found the stability of modified CAGB in the air and in electrolyte solutions was greatly improved.

  14. Module for dielectric surfaces modification by fast neutral particles beams

    Science.gov (United States)

    Barchenko, V. T.; Lisenkov, A. A.; Babinov, N. A.

    2014-11-01

    In this paper, we describe the module for dielectric and wide-gap semiconductor surfaces modification by fast neutral beam. The module can be used for cleaning, etching or assisting of films deposition. The surface proceeding by neutral beam can prevent an accumulation of surface charge without using current compensation by inserting electrons to the beam or RF power supply. The module beside cathode and anode contains an electrode with floating potential. Insertion of the additional electrode causes electron retention in an electrostatic trap resulting the reducing of the module operating pressure. Moreover, the electrode with floating potential allows increasing the current efficient of the module. An important feature of the module is that neutralization of the ions extracted from the plasma occurs in the cathode potential well. Thereby ions that have not neutralized cannot leave nearcathode region and there are no fast ions in the output beam. Module does not contain sources of the magnetic fields or elements heated by external sources. Module operates with free cooling. Thus, the module does not need water cooling and can be freely moved in the vacuum chamber.

  15. Surface modification of polypropylene membrane by polyethylene glycol graft polymerization.

    Science.gov (United States)

    Abednejad, Atiye Sadat; Amoabediny, Ghasem; Ghaee, Azadeh

    2014-09-01

    Polypropylene hollow fiber microporous membranes have been used in a wide range of applications, including blood oxygenator. The hydrophobic feature of the polypropylene surface causes membrane fouling. To minimize fouling, a modification consisting of three steps: surface activation in H2 and O2 plasma, membrane immersion in polyethylene glycol (PEG) and plasma graft polymerization was performed. The membranes were characterized by contact angle measurement, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), tensile test, scanning electron microscopy (SEM) and atomic force microscopy (AFM). Oxygen transfer of modified membranes was also tested. The stability of grafted PEG was measured in water and in phosphate buffer saline (PBS) at 37°C. Blood compatibility of modified surfaces was evaluated by the platelet adhesion method. Water contact angel reduction from 110° to 72° demonstrates the enhanced hydrophilicity, and XPS results verify the presence of oxygenated functional groups due to the peak existence in 286 eV as a result of PEG grafting. The results clearly indicate that plasma graft-polymerization of PEG is an effective way for antifouling improvement of polypropylene membranes. Also, the results show that oxygen transfer changes in PEG grafted membranes are not significant.

  16. Surface modification by plasma polymerization: film deposition, tailoring of surface properties and biocompatibility

    NARCIS (Netherlands)

    Os, van Menno Thomas

    2000-01-01

    The work described in this thesis concerns the surface modification of materials by thin film deposition in a plasma reactor. In particular, thin polymeric films bearing amine functionalities were synthesized by plasma polymerization of amino group containing monomers. In addition to the synthesis,

  17. Modification of polyamide-CdS-CdSe composite material films with Ag using a cation–cation exchange reaction

    Energy Technology Data Exchange (ETDEWEB)

    Krylova, V.; Žalenkienė, S.; Dukstienė, N. [Department of Physical and Inorganic Chemistry, Kaunas University of Technology, Radvilenu st. 19, LT-50254, Kaunas (Lithuania); Baltrusaitis, J., E-mail: job314@lehigh.edu [Department of Chemical and Biomolecular Engineering, Lehigh University, B336 Iacocca Hall, 111 Research Drive, Bethlehem, PA 18015 (United States)

    2015-10-01

    Highlights: • We investigated deposition of a mixed CdSe-CdS-Ag{sub 2}Se-Ag{sub 2}S on polyamide. • A single chalcogen precursor – K{sub 2}SeS{sub 2}O{sub 6} – was used. • AAS showed five- to ten-fold excess of chalcogens diffused into PA. • Addition of AgNO{sub 3} resulted in subsurface Ag{sub 2}Se–Ag{sub 2}S formation. - Abstract: Thin mixed CdSe-CdS-Ag{sub 2}Se-Ag{sub 2}S films were deposited on a polyamide 6 (PA) surface by successfully using a cation-exchange reaction between Cd{sup 2+} and Ag{sup +} to convert CdSe-CdS into Ag{sub 2}Se-Ag{sub 2}S. These were deposited using a K{sub 2}SeS{sub 2}O{sub 6} precursor solution at 60 °C followed by cadmium acetate (Cd(CH{sub 3}COO){sub 2}). An aqueous AgNO{sub 3} solution was used as the Ag source. XRD patterns showed a complex PA-Cd-S-Se-Ag film crystalline composition with CdS, CdSe, Ag{sub 2}S and Ag{sub 2}Se peaks. Calculated dislocation density ranged within 5–15 × 10{sup 13} lines·m{sup −2} indicating high quality atomic layers. Atomic Absorption Spectroscopy (AAS) showed five- to ten-fold excess of chalcogens to metals in the thin films formed. No chalcogenides were observed on the sample surface during XPS analysis after Ag exchange due to the desorption of CdS and CdSe layers, not diffused into the bulk of the polymer suggesting that silver chalcogenides were located subsurface, as opposed to the outermost layer, likely comprised of Ag{sub 2}O.

  18. Surface modification of polypropylene membrane by polyethylene glycol graft polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Abednejad, Atiye Sadat, E-mail: atiyeabednejad@gmail.com [Department of Biomedical Engineering, Faculty of New Sciences and Technologies, University of Tehran, P.O. Box 14395-1561, Tehran (Iran, Islamic Republic of); Amoabediny, Ghasem [Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, P.O. Box 14395-1561, Tehran (Iran, Islamic Republic of); Research Center for New Technologies in Life Science Engineering, University of Tehran, P.O. Box 63894-14179, Tehran (Iran, Islamic Republic of); Ghaee, Azadeh [Department of Biomedical Engineering, Faculty of New Sciences and Technologies, University of Tehran, P.O. Box 14395-1561, Tehran (Iran, Islamic Republic of)

    2014-09-01

    Polypropylene hollow fiber microporous membranes have been used in a wide range of applications, including blood oxygenator. The hydrophobic feature of the polypropylene surface causes membrane fouling. To minimize fouling, a modification consisting of three steps: surface activation in H{sub 2} and O{sub 2} plasma, membrane immersion in polyethylene glycol (PEG) and plasma graft polymerization was performed. The membranes were characterized by contact angle measurement, Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), tensile test, scanning electron microscopy (SEM) and atomic force microscopy (AFM). Oxygen transfer of modified membranes was also tested. The stability of grafted PEG was measured in water and in phosphate buffer saline (PBS) at 37 °C. Blood compatibility of modified surfaces was evaluated by the platelet adhesion method. Water contact angel reduction from 110° to 72° demonstrates the enhanced hydrophilicity, and XPS results verify the presence of oxygenated functional groups due to the peak existence in 286 eV as a result of PEG grafting. The results clearly indicate that plasma graft-polymerization of PEG is an effective way for antifouling improvement of polypropylene membranes. Also, the results show that oxygen transfer changes in PEG grafted membranes are not significant. - Highlights: • H{sub 2} and O{sub 2} plasma graft polymerization of PEG on polypropylene membrane was carried out. • Changes in surface properties were investigated by FTIR, XPS, SEM, and AFM. • Surface wettability enhanced as a result of poly ethylene glycol grafting. • PEG grafting degree increase causes reduction of fouling and adhesion.

  19. Polyamide desalination membrane characterization and surface modification to enhance fouling resistance.

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Mukul M. (Univeristy of Texas at Austin, Austin, TX); Freeman, Benny D. (Univeristy of Texas at Austin, Austin, TX); Van Wagner, Elizabeth M. (Univeristy of Texas at Austin, Austin, TX); Hickner, Michael A. (Pennsylvania State University, University Park, PA); Altman, Susan Jeanne

    2010-08-01

    The market for polyamide desalination membranes is expected to continue to grow during the coming decades. Purification of alternative water sources will also be necessary to meet growing water demands. Purification of produced water, a byproduct of oil and gas production, is of interest due to its dual potential to provide water for beneficial use as well as to reduce wastewater disposal costs. However, current polyamide membranes are prone to fouling, which decreases water flux and shortens membrane lifetime. This research explored surface modification using poly(ethylene glycol) diglycidyl ether (PEGDE) to improve the fouling resistance of commercial polyamide membranes. Characterization of commercial polyamide membrane performance was a necessary first step before undertaking surface modification studies. Membrane performance was found to be sensitive to crossflow testing conditions. Concentration polarization and feed pH strongly influenced NaCl rejection, and the use of continuous feed filtration led to higher water flux and lower NaCl rejection than was observed for similar tests performed using unfiltered feed. Two commercial polyamide membranes, including one reverse osmosis and one nanofiltration membrane, were modified by grafting PEGDE to their surfaces. Two different PEG molecular weights (200 and 1000) and treatment concentrations (1% (w/w) and 15% (w/w)) were studied. Water flux decreased and NaCl rejection increased with PEGDE graft density ({micro}g/cm{sup 2}), although the largest changes were observed for low PEGDE graft densities. Surface properties including hydrophilicity, roughness and charge were minimally affected by surface modification. The fouling resistance of modified and unmodified membranes was compared in crossflow filtration studies using model foulant solutions consisting of either a charged surfactant or an oil in water emulsion containing n-decane and a charged surfactant. Several PEGDE-modified membranes demonstrated improved

  20. Protein adsorption to graphene surfaces controlled by chemical modification of the substrate surfaces.

    Science.gov (United States)

    Kamiya, Yasutaka; Yamazaki, Kenji; Ogino, Toshio

    2014-10-01

    We have investigated effects of the support substrate surfaces on properties of the attached graphene flakes by observing protein adsorption to the graphene surfaces on SiO2/Si substrates that are modified with self-assembled monolayers to control their hydrophilicity. Using atomic force microscopy operated in aqueous environment, we found that high-density clusters of agglomerated avidin molecules form on the graphene flakes in the areas supported by a hydrophobic substrate surface, whereas very low density of large avidin clusters form at the edge of graphene flakes in the area supported by a hydrophilic surface. These results demonstrate that hydrophilicity of the support surface affects hydrophilicity of the graphene surface also in aqueous environment and that surface modification of the support substrate is a useful technique to control protein adsorption phenomena on graphene surfaces for realization of high sensitive graphene biosensors.

  1. Surface modification by plasma polymerization: film deposition, tailoring of surface properties and biocompatibility

    OpenAIRE

    Os, van, J.

    2000-01-01

    The work described in this thesis concerns the surface modification of materials by thin film deposition in a plasma reactor. In particular, thin polymeric films bearing amine functionalities were synthesized by plasma polymerization of amino group containing monomers. In addition to the synthesis, attention was directed towards the characterization of these films, and the tailoring of their surface properties on a molecular level. Finally, the amino groups introduced by plasma polymerization...

  2. A comparative study of biomolecule and polymer surface modifications by a surface microdischarge

    Science.gov (United States)

    Bartis, Elliot A. J.; Luan, Pingshan; Knoll, Andrew J.; Graves, David B.; Seog, Joonil; Oehrlein, Gottlieb S.

    2016-02-01

    Cold atmospheric plasma (CAP) sources are attractive sources of reactive species with promising industrial and biomedical applications, but an understanding of underlying surface mechanisms is lacking. A kHz-powered surface microdischarge (SMD) operating with N2/O2 mixtures was used to study the biological deactivation of two immune-stimulating biomolecules: lipopolysaccharide (LPS) and peptidoglycan (PGN), found in bacteria such as Escherichia coli and Staphylococcus aureus, respectively. Model polymers were also studied to isolate specific functional groups. Changes in the surface chemistry were measured to understand which plasma-generated species and surface modifications are important for biological deactivation. The overall goal of this work is to determine which effects of CAP treatment are generic and which bonds are susceptible to attack. CAP treatment deactivated biomolecules, oxidized surfaces, and introduced surface bound NO3. These effects can be controlled by the N2 fraction in O2 and applied voltage and vary among different target surfaces. The SMD was compared with an Ar/O2/N2-fed kHz-powered atmospheric pressure plasma jet and showed much higher surface modifications and surface chemistry tunability compared to the jet. Possible mechanisms are discussed and findings are compared with recent computational investigations. Our results demonstrate the importance of long-lived plasma-generated species and advance an atomistic understanding of CAP-surface interactions.

  3. Nonadiabatic nuclear dynamics of the ammonia cation studied by surface hopping classical trajectory calculations

    CERN Document Server

    Belyaev, Andrey K; Lasser, Caroline; Trigila, Giulio

    2014-01-01

    The Landau--Zener (LZ) type classical-trajectory surface-hopping algorithm is applied to the nonadiabatic nuclear dynamics of the ammonia cation after photoionization of the ground-state neutral molecule to the excited states of the cation. The algorithm employs the recently proposed formula for nonadiabatic LZ transition probabilities derived from the adiabatic potential energy surfaces. The evolution of the populations of the ground state and the two lowest excited adiabatic states is calculated up to 200 fs. The results agree well with quantum simulations available for the first 100 fs based on the same potential energy surfaces. Four different time scales are detected for the nuclear dynamics: Ultrafast Jahn--Teller dynamics between the excited states on a 5 fs time scale; fast transitions between the excited state and the ground state within a time scale of 20 fs; relatively slow partial conversion of a first-excited-state population to the ground state within a time scale of 100 fs; and nearly constant ...

  4. Biological and surface-active properties of double-chain cationic amino acid-based surfactants.

    Science.gov (United States)

    Greber, Katarzyna E; Dawgul, Małgorzata; Kamysz, Wojciech; Sawicki, Wiesław; Łukasiak, Jerzy

    2014-08-01

    Cationic amino acid-based surfactants were synthesized via solid phase peptide synthesis and terminal acylation of their α and ε positions with saturated fatty acids. Five new lipopeptides, N-α-acyl-N-ε-acyl lysine analogues, were obtained. Minimum inhibitory concentration and minimum bactericidal (fungicidal) concentration were determined on reference strains of bacteria and fungi to evaluate the antimicrobial activity of the lipopeptides. Toxicity to eukaryotic cells was examined via determination of the haemolytic activities. The surface-active properties of these compounds were evaluated by measuring the surface tension and formation of micelles as a function of concentration in aqueous solution. The cationic surfactants demonstrated diverse antibacterial activities dependent on the length of the fatty acid chain. Gram-negative bacteria and fungi showed a higher resistance than Gram-positive bacterial strains. It was found that the haemolytic activities were also chain length-dependent values. The surface-active properties showed a linear correlation between the alkyl chain length and the critical micelle concentration.

  5. Nanoscale surface modification of Mt. Etna volcanic ashes

    Science.gov (United States)

    Barone, G.; Mazzoleni, P.; Corsaro, R. A.; Costagliola, P.; Di Benedetto, F.; Ciliberto, E.; Gimeno, D.; Bongiorno, C.; Spinella, C.

    2016-02-01

    Ashes emitted during volcanic explosive activity present peculiar surface chemical and mineralogical features related in literature to the interaction in the plume of solid particles with gases and aerosols. The compositional differences of magmas and gases, the magnitude, intensity and duration of the emission and the physical condition during the eruption, strongly influence the results of the modification processes. Here we report the characterization of the products emitted during the 2013 paroxysmal activity of Mt. Etna. The surface features of the ash particles were investigated through X-ray photoelectron spectroscopy (XPS) and Transmission electron microscopy (TEM) allowing the analysis at nanometer scale. TEM images showed on the surface the presence of composite structures formed by Ca, Mg and Na sulphates and halides and of droplets and crystals of chlorides; nanometric magnesioferrite and metallic iron dendrites are observable directly below the surface. From the chemical point of view, the most external layer of the volcanic glassy particles (XPS, presents depletion in Si, Mg, Ca, Na and K and strong enrichment in volatile elements especially F and S, with respect to the inner zone, which represents the unaltered counterpart. Below this external layer, a transition glassy shell (thick 50-100 nm) is characterized by Fe, Mg and Ca enrichments with respect to the inner zone. We propose that the ash particle surface composition is the result of a sequence of events which start at shallow depth, above the exsolution surface, where gas bubbles nucleate and the interfaces between bubbles and melt represent proto-surfaces of future ash particles. Enrichment of Ca, Mg and Fe and halides may be due to the early partition of F and Cl in the gas phase and their interaction with the melt layer located close to the bubbles. Furthermore the formation of volatile SiF4 and KF explain the observed depletion of Si and K. The F enrichment in the external ∼50 nm thick

  6. Effect of chitosan and cationic starch on the surface chemistry properties of bagasse paper.

    Science.gov (United States)

    Ashori, Alireza; Cordeiro, Nereida; Faria, Marisa; Hamzeh, Yahya

    2013-07-01

    The use of non-wood fibers in the paper industry has been an economical and environmental necessity. The application of dry-strength agents has been a successful method to enhance the strength properties of paper. The experimental results evidencing the potential of chitosan and cationic starch utilization in bagasse paper subjected to hot water pre-extraction has been presented in this paper. The research analyzes the surface properties alterations due to these dry-strength agents. Inverse gas chromatography was used to evaluate the properties of surface chemistry of the papers namely the surface energy, active sites, surface area as well as the acidic/basic character. The results of the study revealed that the handsheets process causes surface arrangement and orientation of chemical groups, which induce a more hydrophobic and basic surface. The acid-base surface characteristics after the addition of dry-strength agents were the same as the bagasse handsheets with and without hot water pre-extraction. The results showed that the dry-strength agent acts as a protecting film or glaze on the surfaces of bagasse paper handsheets.

  7. Surface modification of titanium dioxide for electrophoretic particles

    Institute of Scientific and Technical Information of China (English)

    PENG Xuhui; LE Yuan; BIAN Shuguang; LI Woyuan; WU Wei; DAI Haitao; CHEN Jianfeng

    2007-01-01

    To prepare stable electrophoretic ink (E Ink)needs color particles to be uniformly dispersed in the organic medium.Thus,t-he modification of inorganic particle surface is required.In this paper,Titanium dioxide modified by alumina has been studied.The surface composition and structures of modified particles have been characterized by X-ray photoelectron spectrometer (XPS),X-ray diffractometer (XRD) and Fourier transform infrared spectrometer (FT-IR).The dispersibility and electrophoretic mobility of these particles in tetrachloroethylene (TCE) have been investigated by laser particle size analyzer,static sedimentation and electrophoretic instrument.Effects of temperature,pH value and stirring rate on the dispersibility and the charge property of samples have been discussed.The results indicate the settle time of modified TiO2 can last 120 h with the response time of 35 s under the optimized modifying conditions,in which temperature is 85℃-90℃,pH is 8-9 and stirring rate is have been significantly improved,which means that the modified TiO2 is suitable for electrophoretic ink particles.

  8. Surface modification of halloysite nanotubes with dopamine for enzyme immobilization.

    Science.gov (United States)

    Chao, Cong; Liu, Jindun; Wang, Jingtao; Zhang, Yanwu; Zhang, Bing; Zhang, Yatao; Xiang, Xu; Chen, Rongfeng

    2013-11-13

    Halloysite nanotubes (HNTs) have been proposed as a potential support to immobilize enzymes. Improving enzyme loading on HNTs is critical to their practical applications. Herein, we reported a simple method on the preparation of high-enzyme-loading support by modification with dopamine on the surface of HNTs. The modified HNTs were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy analyses. The results showed that dopamine could self-polymerize to adhere to the surface of HNTs and form a thin active coating. While the prepared hybrid nanotubes were used to immobilize enzyme of laccase, they exhibited high loading ability of 168.8 mg/g support, which was greatly higher than that on the pristine HNTs (11.6 mg/g support). The immobilized laccase could retain more than 90% initial activity after 30 days of storage and the free laccase only 32%. The immobilized laccase could also maintain more than 90% initial activity after five repeated uses. In addition, the immobilized laccase exhibited a rapid degradation rate and high degradation efficiency for removal of phenol compounds. These advantages indicated that the new hybrid material can be used as a low-cost and effective support to immobilize enzymes.

  9. Adsorption of sodium ions and hydrated sodium ions on a hydrophobic graphite surface via cation-π interactions

    Institute of Scientific and Technical Information of China (English)

    Shi Guo-Sheng; Wang Zhi-Gang; Zhao Ji-Jun; Hu Jun; Fang Hai-Ping

    2011-01-01

    Using density functional theory computation, we show that sodium ions and hydrated sodium ions can be strongly adsorbed onto a hydrophobic graphite surface via cation-π interactions. The key to this cation-π interaction is the coupling of the delocalized π states of graphite and the empty orbitals of sodium ions. This finding implies that the property of the graphite surface is extremely dependent on the existence of the ions on the surface, suggesting that the hydrophobic property of the graphite surface may be affected by the existence of the sodium ions.

  10. Surface membrane traffic in guinea pig basophils exposed to cationic ferritin.

    Science.gov (United States)

    Dvorak, A M; Dvorak, H F; Galli, S J

    1985-01-01

    Surface membrane traffic patterns can be influenced by a number of factors, including the functional state of the cell. We used transmission electron microscopy to investigate the fate of surface membrane in guinea pig basophils exposed to cationized ferritin (CF) in vitro. CF bound to the plasma membrane and was internalized on the membranes of vesicles and vacuoles, a process that was particularly prominent at the uropod of basophils exhibiting a polarized ('motile') configuration. The vesicles/vacuoles moved to the Golgi area, or, in the case of degranulating basophils, were observed in continuity with the degranulation sac, a structure formed largely by the fusion of individual cytoplasmic granule membranes. However, CF-positive vesicles were never observed to fuse directly with the membranes of intact cytoplasmic granules.

  11. Surface modifications of the Sima de los Huesos fossil humans.

    Science.gov (United States)

    Andrews, P; Fernandez Jalvo, Y

    1997-01-01

    The sample of fossil human bones from the Sima de los Huesos, Atapuerca, has been analysed to trace parts of its taphonomic history. The work reported here is restricted to analysis of the skeletal elements preserved and their surface modifications. Preliminary plans of specimen distribution published 6 years ago indicate that the skeletal elements are dispersed within the cave, but more recent data are not yet available. Most of the fossils are broken, with some breakage when the bone was fresh and some when already partly mineralized, both types showing some rounding. There are few longitudinal breaks on shafts of long bones and so very few bone splinters. All skeletal elements are preserved but in unequal proportions, with elements like femora, humeri and mandibles and teeth with greater structural density being best represented. There is no evidence of weathering or of human damage such as cut marks on any of the human assemblage, but trampling damage is present on most bones. Carnivore damage is also common, with some present on more than half the sample, but it is mostly superficial, either on the surfaces of shafts and articular ends or on the edges of spiral breaks. The sizes and distribution of the carnivore pits indicate extensive canid activity, and this is interpreted as scavenging of the bones in place in the cave. Indications of tooth marks from a larger carnivore indicate the activity possibly of a large felid: the marks are too large to be produced by small canids, with the larger marks concentrated on spiral breaks on the more robust bones, and there is no evidence of bone crushing and splintering in the manner of hyaenas. The nature of the SH human assemblage is also consistent with accumulation by humans, the evidence for this being the lack of other animals, especially the lack of herbivorous animals, associated with the humans, and the high number of individuals preserved.

  12. NafionTM膜表面改性用等离子体聚合方法提高膜的阳离子选择性%Surface Modification of Ion Exchange Membrane(NafionTM) The Enhancement of Cation Selectivity by Plasma Polymerization Process

    Institute of Scientific and Technical Information of China (English)

    曾蓉; 朱鹤孙; 庞志成; 弋峰

    2001-01-01

    An ultra-thin anionic exchange layer containing —NH2 and —CONH2 was deposited on the surface of NafionTM membrane. This layer was deposited from ethylene and ammonia using a glow-discharge plasma polymerization technique. The SEM, ATR(attenuated total reflection) spectra and XPS(X-ray photoelectron spectroscopy) showed that the resulted plasma polymers containing —NH2 and —CONH2 was about 0.5 μm thick. The proton perm-selectivity of plasma-modified NafionTM membrane was expressed by tCu, the transference number of the Cu2+ ion through the membrane which was determined by using NafionTM membrane as the separator in a typical two-compartment cell(0.25 mol/L CuCl2-0.5mol/L HCl|plasma-modified NafionTM membrane|1 mol/L HCl). Pretreatment of the NafionTM membrane by oxygen sputtering enhanced the adhesion of plasma polymer onto its surface. The plasma-treated membrane exhibited a high perm-selectivity and its resistance in 1 mol/L HCl was only a little bit higher than NafionTM membrane(<0.5 Ω*cm2).%采用辉光放电等离子体聚合方法, 以C2H4和NH3为单体, 在NafionTM膜表面沉积一层含氨基及酰氨基的类聚乙烯阴离子交换膜, 提高了NafionTM膜对阳离子的选择性, 同时不显著增加膜电阻. 由SEM确定该等离子体聚合膜厚约0.5 μm, 用红外光谱及X光电子能谱表征膜结构. 采用四电极法测量膜电阻, 膜对质子的选择性由Cu2+的迁移数tCu表征, 用二室隔膜装置(0.25 mol/L CuCl2-0.5 mol/L HCl|等离子体处理膜|1 mol/L HCl)测量tCu. O2等离子体预处理NafionTM膜有利于沉积膜在NafionTM膜上的沉积并与NafionTM膜紧密结合. 经改性后的NafionTM膜电阻值仍然很小, 在1 mol/L HCl溶液中电阻小于0.5 Ω*cm2.

  13. Surface and antitumor activity of some novel metal-based cationic surfactants

    Directory of Open Access Journals (Sweden)

    Badawi A

    2007-01-01

    Full Text Available The development of anticancer metal-based drugs was attempted by reacting dodecyl amine with selenious acid to produce a quaternary ammonium salt which was then converted to copper and cobalt cationic complexes via complexing the first compounds with copper (II or cobalt (II ions. The surface properties of these surfactants were investigated. The surface properties studied included critical micelle concentration (CMC, maximum surface excess (Γmax , and minimum surface area (Amin . Free energy of micellization (∆G o mic and adsorption (∆Go ads were calculated. Antitumor activity was tested by using Ehrlich ascites carcinoma (EAC as a model system of mice cell tumor. The compounds were also tested in vitro on five human monolayer tumor cell lines: MCF 7 (breast carcinoma, HEPG 2 (liver carcinoma, U 251 (brain tumor, HCT116 (colon carcinoma, and H460 (lung carcinoma. FTIR spectra, elemental analysis, and H 1 NMR spectra were performed to insure the purity of the prepared compounds.

  14. Determination of anionic surface active agents using silica coated magnetite nanoparticles modified with cationic surfactant aggregates.

    Science.gov (United States)

    Pena-Pereira, Francisco; Duarte, Regina M B O; Trindade, Tito; Duarte, Armando C

    2013-07-19

    The development of a novel methodology for extraction and preconcentration of the most commonly used anionic surface active agents (SAAs), linear alkylbenzene sulfonates (LAS), is presented herein. The present method, based on the use of silica-magnetite nanoparticles modified with cationic surfactant aggregates, was developed for determination of C10-C13 LAS homologues. The proposed methodology allowed quantitative recoveries of C10-C13 LAS homologues by using a reduced amount of magnetic nanoparticles. Limits of detection were in the range 0.8-1.9μgL(-1) for C10-C13 LAS homologues, while the repeatability, expressed as relative standard deviation (RSD), ranged from 2.0 to 3.9% (N=6). Finally, the proposed method was successfully applied to the analysis of a variety of natural water samples.

  15. Studies on polyurethane adhesives and surface modification of hydrophobic substrates

    Science.gov (United States)

    Krishnamoorthy, Jayaraman

    studies involved making functionalized, thickness-controlled, wettability-controlled multilayers on hydrophobic substrates and the adsorption of carboxylic acid-terminated poly(styrene-b-isoprene) on alumina/silica substrates. Poly(vinyl alcohol) has been shown to adsorb onto hydrophobic surfaces irreversibly due to hydrophobic interactions. This thin semicrystalline coating is chemically modified using acid chlorides, butyl isocyanate and butanal to form thicker and hydrophobic coatings. The products of the modification reactions allow adsorption of a subsequent layer of poly(vinyl alcohol) that could subsequently be hydrophobized. This 2-step (adsorption/chemical modification) allows layer-by-layer deposition to prepare coatings with thickness, chemical structure and wettability control on any hydrophobic surface. Research on adsorption characteristics of carboxylic acid-terminated poly(styrene-b-isoprene) involved syntheses of block copolymers with the functional group present at specific ends. Comparative adsorption studies for carboxylic acid-terminated and hydrogen-terminated block copolymers was carried out on alumina and silica substrates.

  16. Plasma Polymerization Surface Modification of Carbon Black and its Effect in Elastomers

    NARCIS (Netherlands)

    Mathew, T.; Datta, R.N.; Dierkes, W.K.; Talma, A.G.; Ooij, van W.J.; Noordermeer, J.W.M.

    2011-01-01

    Surface modification of carbon black by plasma polymerization was aimed to reduce its surface energy in order to compatibilize the filler with various elastomers. A fullerenic carbon black was used for the modification process. Thermogravimetric analysis, wetting behavior with liquids of known surfa

  17. Statistical Modification Analysis of Helical Planetary Gears based on Response Surface Method and Monte Carlo Simulation

    Institute of Scientific and Technical Information of China (English)

    ZHANG Jun; GUO Fan

    2015-01-01

    Tooth modification technique is widely used in gear industry to improve the meshing performance of gearings. However, few of the present studies on tooth modification considers the influence of inevitable random errors on gear modification effects. In order to investigate the uncertainties of tooth modification amount variations on system’s dynamic behaviors of a helical planetary gears, an analytical dynamic model including tooth modification parameters is proposed to carry out a deterministic analysis on the dynamics of a helical planetary gear. The dynamic meshing forces as well as the dynamic transmission errors of the sun-planet 1 gear pair with and without tooth modifications are computed and compared to show the effectiveness of tooth modifications on gear dynamics enhancement. By using response surface method, a fitted regression model for the dynamic transmission error(DTE) fluctuations is established to quantify the relationship between modification amounts and DTE fluctuations. By shifting the inevitable random errors arousing from manufacturing and installing process to tooth modification amount variations, a statistical tooth modification model is developed and a methodology combining Monte Carlo simulation and response surface method is presented for uncertainty analysis of tooth modifications. The uncertainly analysis reveals that the system’s dynamic behaviors do not obey the normal distribution rule even though the design variables are normally distributed. In addition, a deterministic modification amount will not definitely achieve an optimal result for both static and dynamic transmission error fluctuation reduction simultaneously.

  18. Cationic and anionic modifications of oil palm empty fruit bunch fibers for the removal of dyes from aqueous solutions.

    Science.gov (United States)

    Sajab, Mohd Shaiful; Chia, Chin Hua; Zakaria, Sarani; Khiew, Poi Sim

    2013-01-01

    Oil palm empty fruit bunch (EFB) fibers were employed to remove dyes from aqueous solutions via adsorption approaches. The EFB fibers were modified using citric acid (CA) and polyethylenimine (PEI) to produce anionic and cationic adsorbents, respectively. The CA modified EFB fibers (CA-EFB) and PEI-modified EFB fibers (PEI-EFB) were used to study the efficiency in removing cationic methylene blue (MB) and anionic phenol red (PR) from aqueous solutions, respectively, at different pHs, temperatures and initial dye concentrations. The adsorption data for MB on the CA-EFB fitted the Langmuir isotherm, while the adsorption of PR on the PEI-EFB fitted the Freundlich isotherm, suggesting a monolayer and heterogeneous adsorption behavior of the adsorption processes, respectively. Both modified fibers can be regenerated up to seven adsorption/desorption cycles while still providing as least 70% of the initial adsorption capacity.

  19. Modification of an Iranian clinoptilolite nano-particles by hexadecyltrimethyl ammonium cationic surfactant and dithizone for removal of Pb(II) from aqueous solution.

    Science.gov (United States)

    Anari-Anaraki, Mostafa; Nezamzadeh-Ejhieh, Alireza

    2015-02-15

    Natural clinoptilolite tuff was mechanically converted to micro (MCP) and nano (NCP) particles. The MCP and NCP powders were respectively modified with hexadecyltrimethyl ammonium bromide (HDTMA) and dithizone (DTZ). The raw and modified samples were characterized by X-ray diffraction (XRD), Fourier transformation infra red (FT-IR), scanning electron microscope (SEM), transmission electron microscope (TEM) and thermogravimetry (TG) and used for the removal of Pb(II) from aqueous solution. The results confirm that both ion exchange and complexation processes are responsible for removal of Pb(II) cations in the modified samples, while Pb(II) cations were only removed via an ion exchange process by the raw clinoptilolite. In this sorbent, the anionic removal property of surfactant modified zeolites (SMZs) changed to cationic removal property by an additional modification step. The best removal efficiency was observed by NCP-HDTMA-DTZ at the following experimental conditions: C(Pb(II)): 800 mg L(-1), HDTMA dosage: 0.2 mol L(-1), DTZ dosage: 5 mmol L(-1), contact time of DTZ with NCP-HDTMA: 1800 min and contact time of the sorbent with Pb(II): 360 min. The NCP-HDTMA-DTZ sorbent showed good efficiency for the removal of lead in the presence of different multivalent cations. Adsorption isotherms of Pb(II) ions obey the Langmuir equation that indicate the monolayer sorption of Pb(II). The adsorption kinetics based on the pseudo-second-order rate equation indicates that the rate limiting step involving a chemical reaction. The negative ΔH and ΔG indicate an exothermic and spontaneous process.

  20. Application of plasma surface modification techniques to improve hemocompatibility of vascular grafts: A review.

    Science.gov (United States)

    Solouk, Atefeh; Cousins, Brian G; Mirzadeh, Hamid; Seifalian, Alexander M

    2011-01-01

    Surface modification using plasma processing can significantly change the chemical and physical characteristics of biomaterial surfaces. When used in combination with additional modification techniques such as direct chemical or biochemical methods, it can produce novel biomaterial surfaces, which are anticoagulant, bioactive, and biomimetic in nature. This article reviews recent advances in improving hemocompatibility of biomaterials by plasma surface modification (PSM). The focus of this review is on PSM of the most commonly used polymers for vascular prostheses such as expanded polytetrafluoroethylene (PTFE), polyethylene terephthalate (Dacron(®) ), and next generation of biomaterials, including polyhedral oligomeric silsesquioxane nanocomposite.

  1. Attenuating the surface Urban Heat Island within the Local Thermal Zones through land surface modification.

    Science.gov (United States)

    Wang, Jiong; Ouyang, Wanlu

    2017-02-01

    Inefficient mitigation of excessive heat is attributed to the discrepancy between the scope of climate research and conventional planning practice. This study approaches this problem at both domains. Generally, the study, on one hand, claims that the climate research of the temperature phenomenon should be at local scale, where implementation of planning and design strategies can be more feasible. On the other hand, the study suggests that the land surface factors should be organized into zones or patches, which conforms to the urban planning and design manner. Thus in each zone, the land surface composition of those excessively hot places can be compared to the zonal standard. The comparison gives guidance to the modification of the land surface factors at the target places. Specifically, this study concerns the Land Surface Temperature (LST) in Wuhan, China. The land surface is classified into Local Thermal Zones (LTZ). The specifications of temperature sensitive land surface factors are relative homogeneous in each zone and so is the variation of the LST. By extending the city scale analysis of Urban Heat Island into local scale, the Local Surface Urban Heat Islands (LSUHIs) are extracted. Those places in each zone that constantly maintain as LSUHI and exceed the homogenous LST variation are considered as target places or hotspots with higher mitigation or adaptation priority. The operation is equivalent to attenuate the abnormal LST variation in each zone. The framework is practical in the form of prioritization and zoning, and mitigation strategies are essentially operated locally.

  2. CATION-EXCHANGE MEMBRANES WITH POLYANILINE SURFACE LAYER FOR WATER TREATMENT

    Directory of Open Access Journals (Sweden)

    Dinar Dilshatovich Fazullin

    2014-01-01

    Full Text Available Ion-exchange membranes are widely used in modern technologies, particularly in the field of water treatment and make it possible to considerably reduce expenses for wastewater treatment and ensure high degree of purification. Currently, perfluorinated sulfated proton-conducting membranes are often used, such as NAFION and its Russian analogue, MF-4SK based on co-polymerization product of a perfluorinated vinyl ether with tetrafluoroethylene. However, with development of the industry, materials with improved properties and lower cost are required. The aim is to obtain ion-exchange membranes for water treatment from metal ions and to study physico-chemical properties of obtained membranes. In this study, cation exchange composite membranes with modified polyaniline surface layer on nylon and PTFE substrate have been obtained. Changes in the structure of membranes were recorded using a microscope. Throughput capacity of the membranes was determined by passing a certain volume of distilled water through the membrane. The experiment intended to determine electivity of membranes was performed by passing a certain volume of metal salt solutions of a known concentration, after which the filtrate was collected. Concentrations of the studied metal ions in the original solution and in the filtrate were determined by the method of atomic adsorptive spectrometry with electro thermal atomization "Quantum Z.ETA". Prepared highly selective ion exchange membranes. Properties of modified membranes, such as selective permeability and ion-exchange capacity have been determined. The membranes feature high selectivity for heavy metal ions. Moisture-retaining power and swelling ability of the membranes have been studied. Selectivity of the membrane to heavy metal ions is between 70 and 99%. Ion-exchange capacity of the obtained nylon polyaniline membrane is not inferior to some commercially available cation-exchange membranes. Use of the modified membranes in the

  3. Surface chemical and physical modification in stent technology for the treatment of coronary artery disease.

    Science.gov (United States)

    Nazneen, Feroze; Herzog, Grégoire; Arrigan, Damien W M; Caplice, Noel; Benvenuto, Pasquale; Galvin, Paul; Thompson, Michael

    2012-10-01

    Coronary artery disease (CAD) kills millions of people every year. It results from a narrowing of the arteries (stenosis) supplying blood to the heart. This review discusses the merits and limitations of balloon angioplasty and stent implantation, the most common treatment options for CAD, and the pathophysiology associated with these treatments. The focus of the review is heavily placed on research efforts geared toward the modification of stent surfaces for the improvement of stent-vascular compatibility and the reduction in the occurrence of related pathophysiologies. Such modifications may be chemical or physical, both of which are surveyed here. Chemical modifications may be passive or active, while physical modification of stent surfaces can also provide suitable substrates to manipulate the responses of vascular cells (endothelial, smooth muscle, and fibroblast). The influence of micro- and nanostructured surfaces on the in vitro cell response is discussed. Finally, future perspectives on the combination of chemical and physical modifications of stent surfaces are also presented.

  4. Surface Modifications of Support Partitions for Stabilizing Biomimetic Membrane Arrays

    DEFF Research Database (Denmark)

    Perry, Mark; Hansen, Jesper Schmidt; Jensen, Karin Bagger Stibius;

    2011-01-01

    Black lipid membrane (BLM) formation across apertures in an ethylene tetra-fluoroethylene (ETFE) partition separating two aqueous compartments is an established technique for the creation of biomimetic membranes. Recently multi-aperture BLM arrays have attracted interest and in order to increase...... modified partitions were similar and significantly lower than for arrays formed using untreated ETFE partitions. For single side n-hexene modification average membrane array lifetimes were not significantly changed compared to untreated ETFE. Double-sided n-hexene modification greatly improved average...... membrane array lifetimes compared to membrane arrays formed across untreated ETFE partitions. n-hexene modifications resulted in BLM membrane arrays which over time developed significantly lower conductance (Gm) and higher capacitance (Cm) values compared to the other membranes with the strongest effect...

  5. Surface modification and characterization for dispersion stability of inorganic nanometer-scaled particles in liquid media

    Directory of Open Access Journals (Sweden)

    Hidehiro Kamiya and Motoyuki Iijima

    2010-01-01

    Full Text Available Inorganic nanoparticles are indispensable for science and technology as materials, pigments and cosmetics products. Improving the dispersion stability of nanoparticles in various liquids is essential for those applications. In this review, we discuss why it is difficult to control the stability of nanoparticles in liquids. We also overview the role of surface interaction between nanoparticles in their dispersion and characterization, e.g. by colloid probe atomic force microscopy (CP-AFM. Two types of surface modification concepts, post-synthesis and in situ modification, were investigated in many previous studies. Here, we focus on post-synthesis modification using adsorption of various kinds of polymer dispersants and surfactants on the particle surface, as well as surface chemical reactions of silane coupling agents. We discuss CP-AFM as a technique to analyze the surface interaction between nanoparticles and the effect of surface modification on the nanoparticle dispersion in liquids.

  6. Surface modification and characterization for dispersion stability of inorganic nanometer-scaled particles in liquid media

    Energy Technology Data Exchange (ETDEWEB)

    Kamiya, Hidehiro; Iijima, Motoyuki, E-mail: kamiya@cc.tuat.ac.j [Institute of Engineering, Tokyo University of Agriculture and Technology, Koganei, Tokyo 184-8588 (Japan)

    2010-08-15

    Inorganic nanoparticles are indispensable for science and technology as materials, pigments and cosmetics products. Improving the dispersion stability of nanoparticles in various liquids is essential for those applications. In this review, we discuss why it is difficult to control the stability of nanoparticles in liquids. We also overview the role of surface interaction between nanoparticles in their dispersion and characterization, e.g. by colloid probe atomic force microscopy (CP-AFM). Two types of surface modification concepts, post-synthesis and in situ modification, were investigated in many previous studies. Here, we focus on post-synthesis modification using adsorption of various kinds of polymer dispersants and surfactants on the particle surface, as well as surface chemical reactions of silane coupling agents. We discuss CP-AFM as a technique to analyze the surface interaction between nanoparticles and the effect of surface modification on the nanoparticle dispersion in liquids. (topical review)

  7. A novel liposome surface modification agent that prolongs blood circulation and retains surface ligand reactivity.

    Science.gov (United States)

    Ishihara, Atsushi; Yamauchi, Masahiro; Tsuchiya, Tomoko; Mimura, Yukiteru; Tomoda, Yutaka; Katagiri, Ayato; Kamiya, Masaaki; Nemoto, Hisao; Suzawa, Toshiyuki; Yamasaki, Motoo

    2012-01-01

    Liposomes are recognized as potentially useful drug carriers but many problems preclude practical medical application. Liposomes bind with serum proteins (opsonization) and are captured by the reticuloendothelial system cells in the liver and spleen, which limits their ability to deliver drugs to other target sites. Modification of lipids with flexible, hydrophilic polymers such as poly(ethylene glycol) (PEG) to yield sterically stabilized liposomes is one approach to improve liposome blood circulation and tissue distribution properties. In this study, we examined liposomes prepared using lipids modified with a new branched oligoglycerol (BGL) moiety for steric stabilization. This novel BGL comprised 14 glycerol units (termed BGL014) connected with flexible ether linkages, resulting in a branched cascade-like structure that is highly expanded in aqueous solution. BGL014 was coupled to 1,2-distearoylphosphatidylethanolamine to yield BGL014-modified lipids. Incorporation of BGL014 into liposomes (BGL014L) resulted in long blood circulation times, despite a much thinner fixed aqueous layer thickness compared to PEG formulations. BGL014 produced a liposome surface coating that appears to function through steric inhibition of non-specific protein binding without strong interference of specific protein-binding reactions. Liposome structure and functionality was maintained following BGL014-modification, as the incorporation ratio of drug remained high. These results suggest that the BGL014 modification of liposomes is a promising approach to produce stable and long circulating drug carriers capable of selective binding to specific proteins.

  8. PET表面改性研究进展%Research progress in PET surface modification

    Institute of Scientific and Technical Information of China (English)

    王甜甜; 王晓春; 赵国樑

    2011-01-01

    The research progress in polyethylene terephthalate ( PET) surface modification was reviewed in China and abroad. The PET surface modification technologies included chemical grafting modification, ultraviolet irradiation grafting modification, high energy irradiation grafting modification, plasma grafting modification and ozone oxidizing modification. The surface modification could improve the hydrophilicity, antistatic behavior, adhesion and biocompatibility of PET. The application of modified PET was introduced in the related fields. It was pointed out that the key scientific and technical problems in PET surface modification should be solved.%综述了国内外聚对苯二甲酸乙二醇酯(PET)的表面改性研究进展.PET表面改性方法主要有:化学接枝改性、紫外光辐照接枝改性、高能射线辐照接枝改性、等离子体处理接枝改性以及臭氧氧化改性等;通过PET表面改性,可以改善PET的亲水性、抗静电性、粘附性和生物相容性等性能;介绍了改性PET在相关领域中的应用;指出PET的表面改性技术尚有许多关键科学问题和技术难题需解决.

  9. Synthesis and surface modification of magnetic particles for application in biotechnology and biomedicine

    Institute of Scientific and Technical Information of China (English)

    Zhiya; Ma; Huizhou; Liu

    2007-01-01

    Magnetic particles have numerous applications in biotechnology and biomedicine. In this paper we reviewed the synthesis, surface modification and some applications of magnetic particles with focus on their synthesis and surface modification. Various methods have been developed for the production of magnetic particles (magnetic nanoparticles and magnetic composite particles). For future application magnetic particles must be modified to obtain stability and surface functional groups. Finally, the application of magnetic particles in magnetic separation, drug delivery,hyperthermia, and magnetic resonance imaging are discussed.

  10. Stability studies of plasma modification effects of polylactide and polycaprolactone surface layers

    Energy Technology Data Exchange (ETDEWEB)

    Moraczewski, Krzysztof, E-mail: kmm@ukw.edu.pl [Kazimierz Wielki University, Chodkiewicza 30, 85-064 Bydgoszcz (Poland); Stepczyńska, Magdalena [Kazimierz Wielki University, Chodkiewicza 30, 85-064 Bydgoszcz (Poland); Malinowski, Rafał [Institute for Engineering of Polymer Materials and Dyes, Marii Skłodowskiej-Curie 55, 87‐100 Toruń (Poland); Rytlewski, Piotr; Jagodziński, Bartłomiej; Żenkiewicz, Marian [Kazimierz Wielki University, Chodkiewicza 30, 85-064 Bydgoszcz (Poland)

    2016-07-30

    Highlights: • Plasma modification affects surface roughness, wettability and surface energy. • Polylactide and polycaprolactone aging causes decay of the modification effects. • Changes in the surface characteristic and wettability deterioration were observed. • The decay occurs due to migration of low molecular weight molecules to the surface. • Plasma modification effect lasts longer in the case of polycaprolactone. - Abstract: The article presents results of research on the stability of oxygen plasma modification effects of polylactide and polycaprolactone surface layers. The modified samples were aged for three, six or nine weeks. The studies were carried out using scanning electron microscopy, goniometry and Fourier transform infrared spectroscopy. Studies have shown that the plasma modification has significant impact on the geometric structure and chemical composition of the surface, wettability and surface energy of tested polymers. The modification effects are not permanent. It has been observed that over time the effects of plasma modification fade. Studies have shown that modifying effect lasts longer in the case of polycaprolactone.

  11. Mechano-activated surface modification of calcium carbonate in wet stirred mill and its properties

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Surface modification of calcium carbonate particles using sodium stearate(SDS) as a modification agent incorporated with the simultaneous wet ultra-fine grinding in the laboratory stirred mill was investigated. The physical properties and application properties of modified calcium carbonate were measured and evaluated. The action mechanism between SDS and calcium carbonate in the modification was studied by infrared spectrometry(IR) and X-ray photoelectron energy spectroscopy(XPS). The results indicate that the crushing mechanic force intensity can obviously influence the modification effect of calcium carbonate because of mechano-chemical effect. The hydrophilic surface of calcium carbonate is turned into hydrophobic after modification. The properties of polyethylene(PE) filled by modified calcium carbonate powder is markedly improved. And the adsorption of SDS could occur by chemical reaction with calcium carbonate surface.

  12. Formation of ZnSe/Bi2Se3 QDs by surface cation exchange and high photothermal conversion

    Directory of Open Access Journals (Sweden)

    Guozhi Jia

    2015-08-01

    Full Text Available Water-dispersed core/shell structure ZnSe/Bi2Se3 quantum dots were synthesized by ultrasonicwave-assisted cation exchange reaction. Only surface Zn ion can be replaced by Bi ion in ZnSe quantum dots, which lead to the ultrathin Bi2Se3 shell layer formed. It is significance to find to change the crystal of QDs due to the acting of ultrasonicwave. Cation exchange mechanism and excellent photothermal conversion properties are discussed in detail.

  13. Structure of DNA-Cationic Surfactant Complexes at Hydrophobically Modified and Hydrophilic Silica Surfaces as Revealed by Neutron Reflectometry

    DEFF Research Database (Denmark)

    Cardenas Gomez, Marite; Wacklin, Hanna; Campbell, Richard A.;

    2011-01-01

    layer structure (the location, coverage, and conformation the e DNA and surfactant molecules). Neutron reflectometry is the technique of choice for revealing the surface layer structure by means of selective deuteration. We start by studying the interfacial complexation of DNA...... with dodecyltrimethylammonium bromide (DTAB) and hexadecyltrimethylammonium bromide (CTAB) on hydrophobic surfaces, where we show that DNA molecules are located on top of a self-assembled surfactant monolayer, with the thickness of the DNA layer and the surfactant DNA ratio determined by the surface coverage of the underlying...... cationic layer. The surface coverages of surfactant and DNA are determined by the bulk concentration of the surfactant relative to its critical micelle concentration (cmc). The structure of the interfacial layer is not affected by the choice of cationic surfactant studied. However, to obtain similar...

  14. Cation-induced monolayer collapse at lower surface pressure follows specific headgroup percolation

    Science.gov (United States)

    Das, Kaushik; Sah, Bijay Kumar; Kundu, Sarathi

    2017-02-01

    A Langmuir monolayer can be considered as a two-dimensional (2D) sheet at higher surface pressure which structurally deform with mechanical compression depending upon the elastic nature of the monolayer. The deformed structures formed after a certain elastic limit are called collapsed structures. To explore monolayer collapses at lower surface pressure and to see the effect of ions on such monolayer collapses, out-of-plane structures and in-plane morphologies of stearic acid Langmuir monolayers have been studied both at lower (≈6.8) and higher (≈9.5) subphase p H in the presence of M g2 +,C a2 +,Z n2 +,C d2 + , and B a2 + ions. At lower subphase p H and in the presence of all cations, the stearic acid monolayer remains as a monolayer before collapse, which generally takes place at higher surface pressure (πc>50 mN /m ). However, at higher subphase p H , structural changes of stearic acid monolayers occur at relatively lower surface pressure depending upon the specific dissolved ions. Among the same group elements of M g2 +,C a2 + , and B a2 + , only for B a2 + ions does monolayer to multilayer transition take place from a much lower surface pressure of the monolayer, remaining, however, as a monolayer for M g2 + and C a2 + ions. For another same group elements of Z n2 + and C d2 + ions, a less covered bilayer structure forms on top of the monolayer structure at lower surface pressure, which is evidenced from both x-ray reflectometry and atomic force microscopy. Fourier transform infrared spectroscopy confirms the presence of two coexisting conformations formed by the two different metal-headgroup coordinations and the monolayer to trilayer or multilayer transformation takes place when the coverage ratio of the two molecular conformations changes from the critical value (pc) of ≈0.66 . Such ion-specific monolayer collapses are correlated with the 2D lattice percolation model.

  15. Controlling electron beam-induced structure modifications and cation exchange in cadmium sulfide–copper sulfide heterostructured nanorods

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Haimei [Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States); Sadtler, Bryce; Habenicht, Carsten [Department of Chemistry, University of California, Berkeley, CA 94720 (United States); Freitag, Bert [FEI Company, P.O. Box 80066, KA 5600 Eindhoven (Netherlands); Alivisatos, A. Paul [Materials Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States); Department of Chemistry, University of California, Berkeley, CA 94720 (United States); Kisielowski, Christian, E-mail: CFKisielowski@lbl.gov [National Center for Electron Microcopy, Lawrence Berkeley National Laboratory, Berkeley, CA 94720 (United States); Joint Center for Artificial Photosynthesis, Berkeley, CA 94720 (United States)

    2013-11-15

    The atomic structure and interfaces of CdS/Cu{sub 2}S heterostructured nanorods are investigated with the aberration-corrected TEAM 0.5 electron microscope operated at 80 kV and 300 kV applying in-line holography and complementary techniques. Cu{sub 2}S exhibits a low-chalcocite structure in pristine CdS/Cu{sub 2}S nanorods. Under electron beam irradiation the Cu{sub 2}S phase transforms into a high-chalcocite phase while the CdS phase maintains its wurtzite structure. Time-resolved experiments reveal that Cu{sup +}–Cd{sup 2+} cation exchange at the CdS/Cu{sub 2}S interfaces is stimulated by the electron beam and proceeds within an undisturbed and coherent sulfur sub-lattice. A variation of the electron beam current provides an efficient way to control and exploit such irreversible solid-state chemical processes that provide unique information about system dynamics at the atomic scale. Specifically, we show that the electron beam-induced copper–cadmium exchange is site specific and anisotropic. A resulting displacement of the CdS/Cu{sub 2}S interfaces caused by beam-induced cation interdiffusion equals within a factor of 3–10 previously reported Cu diffusion length measurements in heterostructured CdS/Cu{sub 2}S thin film solar cells with an activation energy of 0.96 eV. - Highlights: • Heterostructured nanorods were investigated at atomic resolution showing that they are free of extended defects. • Beam–sample interactions are controlled by current and voltage variations to provide pristine crystal structures. • Beam-induced migration of heterointerfaces are measured time-resolved and compared with Cu diffusion coefficients. • Beam–sample interaction overwrite possible signal improvements that can be expected by sample cooling.

  16. Surface Modification of Exfoliated Graphite Nano-Reinforcements Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Phase I results showed that two surface treatments, oxidative plasma and reactive finishes, are effective means of modifying the surface chemistry of exfoliated...

  17. Study of surface modification of uranium and UFe{sub 2} by various surface analysis techniques

    Energy Technology Data Exchange (ETDEWEB)

    Bonino, O.; Dugne, O.; Merlet, C. E-mail: merlet@dstu.univ-montp2.fr; Gat, E.; Holliger, Ph.; Lahaye, M

    2001-04-01

    The surface modification of U, UFe{sub 2} by exposition in air at room temperature and at 63 deg. C was studied by secondary ion mass spectroscopy (SIMS), time of flight-secondary ion mass spectroscopy (ToF-SIMS), Auger electron spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS) with variable detection angle. For the two systems, a first layer of carbon contamination, followed by complex oxide layer constitutes the surface. For U, the oxide layer is composed of a mixture of UO{sub 2} and UO{sub 2+x} with x maximal at the surface. In UFe{sub 2}, the oxide layer is composed of a mixture of UO{sub 2} and UO{sub 2+x}, oxidised iron in Fe2+ and Fe3+ chemical states (more probably FeO), a few percent of a ternary oxide UFeO{sub 4}, and less than 1% of uranium carbide. A surface segregation of uranium is shown in UFe{sub 2}.

  18. Simultaneous Sterilization With Surface Modification Of Plastic Bottle By Plasma-Based Ion Implantation

    Science.gov (United States)

    Sakudo, N.; Ikenaga, N.; Ikeda, F.; Nakayama, Y.; Kishi, Y.; Yajima, Z.

    2011-01-01

    Dry sterilization of polymeric material is developed. The technique utilizes the plasma-based ion implantation which is same as for surface modification of polymers. Experimental data for sterilization are obtained by using spores of Bacillus subtilis as samples. On the other hand we previously showed that the surface modification enhanced the gas barrier characteristics of plastic bottles. Comparing the implantation conditions for the sterilization experiment with those for the surface modification, we find that both sterilization and surface modification are simultaneously performed in a certain range of implantation conditions. This implies that the present bottling system for plastic vessels will be simplified and streamlined by excluding the toxic peroxide water that has been used in the traditional sterilization processes.

  19. AGD Surface Modification on Nanofibers to Improve Dispersion and Interfacial Bonding

    Science.gov (United States)

    2007-05-26

    1091. [9] V. Bruse, M. Heintze, W. Brandl, G. Marginean, H. Bubert, “ Surface modification of carbon nanofibers in low temperature plasmas”, Science direct , Diamond and related materials, (2004), p. 1177 – 1181.

  20. Cation coordination reactions on nanocrystals: surface/interface, doping control and advanced photocatalysis applications (Conference Presentation)

    Science.gov (United States)

    Zhang, Jiatao

    2016-10-01

    Abstract: Including the shape and size effect, the controllable doping, hetero-composite and surface/interface are the prerequisite of colloidal nanocrystals for exploring their optoelectronic properties, such as fluorescence, plasmon-exciton coupling, efficient electron/hole separation, and enhanced photocatalysis applications. By controlling soft acid-base coordination reactions between cation molecular complexes and colloidal nanocrystals, we showed that chemical thermodynamics could drive nanoscale monocrystalline growth of the semiconductor shell on metal nano-substrates and the substitutional heterovalent doping in semiconductor nanocrystals. We have demonstrated evolution of relative position of Au and II-VI semiconductor in Au-Semi from symmetric to asymmetric configuration, different phosphines initiated morphology engineering, oriented attachment of quantum dots into micrometer nanosheets with synergistic control of surface/interface and doing, which can further lead to fine tuning of plasmon-exciton coupling. Therefore, different hydrogen photocatalytic performance, Plasmon enhanced photocatalysis properties have been achieved further which lead to the fine tuning of plasmon-exciton coupling. Substitutional heterovalent doping here enables the tailoring of optical, electronic properties and photocatalysis applications of semiconductor nanocrystals because of electronic impurities (p-, n-type doping) control. References: (1) J. Gui, J. Zhang*, et al. Angew. Chem. Int. Ed. 2015, 54, 3683. (2) Q. Zhao, J. Zhang*, etc., Adv. Mater. 2014, 26, 1387. (3) J. Liu, Q. Zhao, S. G. Wang*, J. Zhang*, etc., Adv. Mater. 2015, 27-2753-2761. (4) H. Qian, J. Zhang*, etc., NPG Asia Mater. (2015) 7, e152. (5) M. Ji, M. Xu, etc., J. Zhang*, Adv. Mater. 2016, in proof. (6) S. Yu, J. T. Zhang, Y. Tang, M. Ouyang*, Nano Lett. 2015, 15, 6282-6288. (7) J. Zhang, Y. Tang, K. Lee and M. Ouyang*, Science 2010, 327, 1634. (8) J. Zhang, Y. Tang, K. Lee, M. Ouyang*, Nature 2010, 466

  1. Surface Modifications and Their Effects on Titanium Dental Implants

    Directory of Open Access Journals (Sweden)

    A. Jemat

    2015-01-01

    Full Text Available This review covers several basic methodologies of surface treatment and their effects on titanium (Ti implants. The importance of each treatment and its effects will be discussed in detail in order to compare their effectiveness in promoting osseointegration. Published literature for the last 18 years was selected with the use of keywords like titanium dental implant, surface roughness, coating, and osseointegration. Significant surface roughness played an important role in providing effective surface for bone implant contact, cell proliferation, and removal torque, despite having good mechanical properties. Overall, published studies indicated that an acid etched surface-modified and a coating application on commercial pure titanium implant was most preferable in producing the good surface roughness. Thus, a combination of a good surface roughness and mechanical properties of titanium could lead to successful dental implants.

  2. Surface Modifications and Their Effects on Titanium Dental Implants.

    Science.gov (United States)

    Jemat, A; Ghazali, M J; Razali, M; Otsuka, Y

    2015-01-01

    This review covers several basic methodologies of surface treatment and their effects on titanium (Ti) implants. The importance of each treatment and its effects will be discussed in detail in order to compare their effectiveness in promoting osseointegration. Published literature for the last 18 years was selected with the use of keywords like titanium dental implant, surface roughness, coating, and osseointegration. Significant surface roughness played an important role in providing effective surface for bone implant contact, cell proliferation, and removal torque, despite having good mechanical properties. Overall, published studies indicated that an acid etched surface-modified and a coating application on commercial pure titanium implant was most preferable in producing the good surface roughness. Thus, a combination of a good surface roughness and mechanical properties of titanium could lead to successful dental implants.

  3. Towards Enhanced Performance Thin-film Composite Membranes via Surface Plasma Modification

    OpenAIRE

    Rackel Reis; Dumée, Ludovic F.; Tardy, Blaise L.; Raymond Dagastine; John D. Orbell; Jürg A. Schutz; Duke, Mikel C.

    2016-01-01

    Advancing the design of thin-film composite membrane surfaces is one of the most promising pathways to deal with treating varying water qualities and increase their long-term stability and permeability. Although plasma technologies have been explored for surface modification of bulk micro and ultrafiltration membrane materials, the modification of thin film composite membranes is yet to be systematically investigated. Here, the performance of commercial thin-film composite desalination membra...

  4. Surface Modification of a PCB Substrate for Better Adhesion of Inkjet Printed Circuit Structures

    OpenAIRE

    Sridhar, A.; Dijk, van, JMF Jan; Akkerman, R.

    2009-01-01

    The robustness and service life of inkjet printed electronic circuit structures are highly influenced by the state of the interface between these structures and the substrate. In the case of polymeric substrate materials, surface modification is necessary to realise a favourable interface, as these materials are generally not very receptive to chemical bond formation with the deposited ink. This paper deals with the surface modification of a high frequency laminate (substrate) using two diffe...

  5. The Aging Study on Polyethylene Terephthalate with Surface Modification by Water Vapor Plasma

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The aging effects of the contact angle and surface energy on polyethylene tereph thalate (PET) have been investigated with surface modification by water vapor plasma. The experimental results show that the contact angle of water and PET decreases obviously and sur face energy increases. However, with the increase of the aging time, the contact angle and surface energy change back gradually to original state.

  6. Microwave plasma surface modification of silicone elastomer with allylamine for improvement of biocompatibility.

    Science.gov (United States)

    Ren, T B; Weigel, Th; Groth, Th; Lendlein, A

    2008-07-01

    The microwave plasma surface modification of silicone elastomer with allylamine was studied to improve the biocompatibility of the material. An effort was made to clarify the relationships among plasma conditions and surface chemical composition, physical surface properties and biocompatibility of material, as well as the stability of plasma deposited layers. ATR-IR, XPS, Ellipsometry measurements, and contact angle measurements were used to investigate the changes of surface. The stability of plasma-treated silicone surfaces were also studied. The results demonstrated that the temperature and pressure had a strong influence on the chemical composition and structure of surface-deposited layer. The layer was nearly completely crosslinking when the modification was carried out at 60 degrees C. The polymerization speed decreased linearly with temperature. The XPS analysis results showed that the nitrogen element content in the surface layer was very high, especially under low pressure. The nitrogen/carbon ratio in the layer even greatly surpassed that of the allylamine monomer. The wettability of the silicone surface was greatly improved after plasma modification, and increased with the quantities of amine groups. The plasma-treated surfaces have good storage stability in air up to 3 months. The wettability of the surfaces decreased incipiently and then it dramatically increased with further time. The human skin fibroblasts were used to evaluate biocompatibility of plasma-treated silicone elastomer. The surface biocompatibility was greatly improved after modification; human skin fibroblasts adhered quickly and grew well on the modified silicone surface.

  7. Surface Modification of Elastomeric Stamps for Microcontact Printing of Polar Inks

    NARCIS (Netherlands)

    Sadhu, Veera Bhadraiah; Perl, András; Peter, Mária; Rozkiewicz, Dorota I.; Engbers, Gerard; Ravoo, Bart Jan; Reinhoudt, David N.; Huskens, Jurriaan

    2007-01-01

    Chemical modification of the surface of a stamp used for microcontact printing (uCP) is interesting for controling the surface properties, such as the hydrophilicity. To print polar inks, plasma polymerization of allylamine (PPAA) was employed to render the surface of poly(dimethylsiloxane) (PDMS),

  8. Chemical modification of a plant origin biomass using cationic surfactant ABDAC and the biosorptive decolorization of RR45 containing solutions.

    Science.gov (United States)

    Akar, Tamer; Ozkara, Esra; Celik, Sema; Turkyilmaz, Serpil; Akar, Sibel Tunali

    2013-01-01

    This study focused on the improvement of the decolorization potential of biomass derived from Pyracantha coccinea. Alkyl benyzldimethyl ammonium chloride (ABDAC) was used as modification agent. Batch mode decolorization potential of modified biosorbent was explored at different operating conditions. ABDAC modification significantly increased the biosorption yield to 97.27%, which was 3.88 times higher than that of natural biomass. The prepared biosorbent was effectively used for the decolorization of Reactive Red 45 contaminated solutions after the optimization of biosorption conditions. The non-linear regression analysis was used to evaluate the isotherm and kinetic model parameters. Process followed the Langmuir isotherm model and the highest monolayer capacity of 152.49 mg g(-1) was obtained with a small amount of modified biosorbent. Kinetic studies indicated fast decolorization rate of the process following the pseudo-first-order model. Biosorption performance of the prepared biosorbent was tested in RR45 containing real wastewater sample. The possible dye biosorbent interactions in the biosorption process were explored by zeta potential, scanning electron microscobe and FTIR analysis.

  9. Superhydrophobic alumina surface based on stearic acid modification

    Energy Technology Data Exchange (ETDEWEB)

    Feng Libang, E-mail: lepond@hotmail.com [School of Mechatronic Engineering, Lanzhou Jiaotong University, Lanzhou 730070 (China); Zhang Hongxia; Mao Pengzhi; Wang Yanping; Ge Yang [School of Mechatronic Engineering, Lanzhou Jiaotong University, Lanzhou 730070 (China)

    2011-02-15

    A novel superhydrophobic alumina surface is fabricated by grafting stearic acid layer onto the porous and roughened aluminum film. The chemical and phase structure, morphology, and the chemical state of the atoms at the superhydrophobic surface were investigated by techniques as FTIR, XRD, FE-SEM, and XPS, respectively. Results show that a super water-repellent surface with a contact angle of 154.2{sup o} is generated. The superhydrophobic alumina surface takes on an uneven flowerlike structure with many nanometer-scale hollows distribute in the nipple-shaped protrusions, and which is composed of boehmite crystal and {gamma}-Al{sub 2}O{sub 3}. Furthermore, the roughened and porous alumina surface is coated with a layer of hydrophobic alkyl chains which come from stearic acid molecules. Therefore, both the roughened structure and the hydrophobic layer endue the alumina surface with the superhydrophobic behavior.

  10. Surface Modification of Titanium Dental Implants by Excimer Laser

    OpenAIRE

    Radnai, M; Bereznai, M.; Pelseczi, I.; Z. Toth; Turzo, K.; Bor, Z.; Fazekas, A

    2002-01-01

    The perfect osseointegration process of the dental implants depends among other factors on the surfact characteristics of the titanium. In this study enlarged mechanical roughness was produced by a laser-based technique, in order to decrease the healing period of the implant. There are different ways of forming laser induced surface structures. In the case of mask projection techniques the surface can be modified in larger areas and surface patterns. An ArF nanosecond excimer laser was use...

  11. Ammonia modification of oxide-free Si(111) surfaces

    Science.gov (United States)

    Chopra, Tatiana Peixoto; Longo, Roberto C.; Cho, Kyeongjae; Chabal, Yves J.

    2016-08-01

    Amination of surfaces is useful in a variety of fields, ranging from device manufacturing to biological applications. Previous studies of ammonia reaction on silicon surfaces have concentrated on vapor phase rather than wet chemical processes, and mostly on clean Si surfaces. In this work, the interaction of liquid and vapor-phase ammonia is examined on three types of oxide-free surfaces - passivated by hydrogen, fluorine (1/3 monolayer) or chlorine - combining infrared absorption spectroscopy, X-ray photoelectron spectroscopy, and first-principles calculations. The resulting chemical composition highly depends on the starting surface; there is a stronger reaction on both F- and Cl-terminated than on the H-terminated Si surfaces, as evidenced by the formation of Si-NH2. Side reactions can also occur, such as solvent reaction with surfaces, formation of ammonium salt by-products (in the case of 0.2 M ammonia in dioxane solution), and nitridation of silicon (in the case of neat and gas-phase ammonia reactions for instance). Unexpectedly, there is formation of Si-H bonds on hydrogen-free Cl-terminated Si(111) surfaces in all cases, whether vapor phase of neat liquid ammonia is used. The first-principles modeling of this complex system suggests that step-edge surface defects may play a key role in enabling the reaction under certain circumstances, despite the endothermic nature for Si-H bond formation.

  12. A Survey of Surface Modification Techniques for Next-Generation Shape Memory Polymer Stent Devices

    Directory of Open Access Journals (Sweden)

    Tina Govindarajan

    2014-08-01

    Full Text Available The search for a single material with ideal surface properties and necessary mechanical properties is on-going, especially with regard to cardiovascular stent materials. Since the majority of stent problems arise from surface issues rather than bulk material deficiencies, surface optimization of a material that already contains the necessary bulk properties is an active area of research. Polymers can be surface-modified using a variety of methods to increase hemocompatibilty by reducing either late-stage restenosis or acute thrombogenicity, or both. These modification methods can be extended to shape memory polymers (SMPs, in an effort to make these materials more surface compatible, based on the application. This review focuses on the role of surface modification of materials, mainly polymers, to improve the hemocompatibility of stent materials; additional discussion of other materials commonly used in stents is also provided. Although shape memory polymers are not yet extensively used for stents, they offer numerous benefits that may make them good candidates for next-generation stents. Surface modification techniques discussed here include roughening, patterning, chemical modification, and surface modification for biomolecule and drug delivery.

  13. Surface modification of tube inner wall by transferred atmospheric pressure plasma

    Science.gov (United States)

    Chen, Faze; Liu, Shuo; Liu, Jiyu; Huang, Shuai; Xia, Guangqing; Song, Jinlong; Xu, Wenji; Sun, Jing; Liu, Xin

    2016-12-01

    Tubes are indispensable in our daily life, mechanical engineering and biomedical fields. However, the practical applications of tubes are sometimes limited by their poor wettability. Reported herein is hydrophilization of the tube inner wall by transferred atmospheric pressure plasma (TAPP). An Ar atmospheric pressure plasma jet (APPJ) is used to induce He TAPP inside polytetrafluoroethylene (PTFE) tube to perform inner wall surface modification. Optical emission spectrum (OES) is used to investigate the distribution of active species, which are known as enablers for surface modification, along the TAPP. Tubes' surface properties demonstrate that after TAPP treatment, the wettability of the tube inner wall is well improved due to the decrease of surface roughness, the removal of surface fluorine and introduction of oxygen. Notably, a deep surface modification can significantly retard the aging of the obtained hydrophilicity. The results presented here clearly demonstrate the great potential of TAPP for surface modification of the inner wall of tube or other hollow bodies, and thus a uniform, effective and long-lasting surface modification of tube with any length can be easily realized by moving the tube along its axis.

  14. Surface modification of magnesium hydroxide by γ-aminopropyltriethoxysilane

    Institute of Scientific and Technical Information of China (English)

    LUO Wei; FENG Qi-ming; OU Le-ming; LIU Kun

    2008-01-01

    Magnesium hydroxide (MH), which is commonly used as a halogen-free flame retardant filler in composite materials, was modified by silanization reaction with γ-aminopropyltriethoxysilane (γ-APS) in aqueous solution at different pH values (pH range from 8.0 to 12.0). The surface properties of grafted γ-APS on MH surface as a function of solution pH value were studied using elemental analysis, Fourier transform infrared spectroscopy and zeta potential measurement. The results show that hydrolysis and condensation of γ-APS are activated in alkaline solution and lead to multilayer adsorption of γ-APS molecules on the surface of MH. The type of adsorption orientation of γ-APS on MH surface is a function of coverage density that is altered by changing solution pH value. At low coverage density (e.g.55nm-2), γ-APS molecules are preferentially adsorbed to the surface with the silicon moiety towards the surface, and increasing coverage density (e.g.90nm-2) leads to parallel orientation. At an even higher coverage density(e.g.115nm-2), γ-APS molecules bond to the surface with the amino moiety towards the surface.

  15. Titanium Alloy Surface Modification by a Spatio-Temporal Atmospheric Pressure DBD Afterglow

    Institute of Scientific and Technical Information of China (English)

    E.PANOUSIS; F.CLEMENT; J.F.LOISEAU; N.SPYROU; B.HELD1; J.LARRIEU; F.GUERTON

    2007-01-01

    The experimental work reported here is devoted to the study of the modifications inflicted on the surface of titanium alloy specimens by an atmospheric pressure dielectric barrier discharge(DBD) reactor in both spatial and temporal afterglow conditions.A commercially available (AcXys Technologies) modified reactor system was used for the surface treatment of the TiA6V4 titanium alloy that is widely used in the aeronautical industry.Wettability surface characterisation and XPS analyses are performed to give a macroscopic and microscopic insight to the surface modifications.Best operating conditions,at constant input energy,were obtained for a duty cycle equal to 10%.

  16. Atomic and molecular layer deposition for surface modification

    Science.gov (United States)

    Vähä-Nissi, Mika; Sievänen, Jenni; Salo, Erkki; Heikkilä, Pirjo; Kenttä, Eija; Johansson, Leena-Sisko; Koskinen, Jorma T.; Harlin, Ali

    2014-06-01

    Atomic and molecular layer deposition (ALD and MLD, respectively) techniques are based on repeated cycles of gas-solid surface reactions. A partial monolayer of atoms or molecules is deposited to the surface during a single deposition cycle, enabling tailored film composition in principle down to molecular resolution on ideal surfaces. Typically ALD/MLD has been used for applications where uniform and pinhole free thin film is a necessity even on 3D surfaces. However, thin - even non-uniform - atomic and molecular deposited layers can also be used to tailor the surface characteristics of different non-ideal substrates. For example, print quality of inkjet printing on polymer films and penetration of water into porous nonwovens can be adjusted with low-temperature deposited metal oxide. In addition, adhesion of extrusion coated biopolymer to inorganic oxides can be improved with a hybrid layer based on lactic acid.

  17. Tailoring radiation damage in ZnO by surface modification

    Science.gov (United States)

    Myers, M. T.; Charnvanichborikarn, S.; Myers, M. A.; Lee, J. H.; Wang, H.; Biener, M. M.; Shao, L.; Kucheyev, S. O.

    2013-07-01

    Heavy-ion irradiation of (0 0 0 1) ZnO crystals results in unusual damage buildup, including an additional (intermediate) peak in damage-depth profiles measured by ion channeling, the formation of near-surface nanocavities, and stoichiometric imbalance. All these effects are thought to be associated with the influence of the sample surface on dynamic annealing processes. Here, by using ion channeling and transmission electron microscopy, we find that placing an ~7 nm thick AlO(OH) layer on the (0 0 0 1) ZnO surface results in (i) suppression of cavity formation, (ii) a reduced intermediate defect peak intensity, and (iii) a decreased level of disorder extending up to ~100 nm from the ZnO surface for room-temperature bombardment with 500 keV Xe ions. Our results demonstrate the potential to control radiation damage in ZnO by surface manipulation.

  18. Identification of Posttranslational Modification-Dependent Protein Interactions Using Yeast Surface Displayed Human Proteome Libraries.

    Science.gov (United States)

    Bidlingmaier, Scott; Liu, Bin

    2015-01-01

    The identification of proteins that interact specifically with posttranslational modifications such as phosphorylation is often necessary to understand cellular signaling pathways. Numerous methods for identifying proteins that interact with posttranslational modifications have been utilized, including affinity-based purification and analysis, protein microarrays, phage display, and tethered catalysis. Although these techniques have been used successfully, each has limitations. Recently, yeast surface-displayed human proteome libraries have been utilized to identify protein fragments with affinity for various target molecules, including phosphorylated peptides. When coupled with fluorescently activated cell sorting and high throughput methods for the analysis of selection outputs, yeast surface-displayed human proteome libraries can rapidly and efficiently identify protein fragments with affinity for any soluble ligand that can be fluorescently detected, including posttranslational modifications. In this review we compare the use of yeast surface display libraries to other methods for the identification of interactions between proteins and posttranslational modifications and discuss future applications of the technology.

  19. Effect of plasma surface modification on the biocompatibility of UHMWPE

    Energy Technology Data Exchange (ETDEWEB)

    Kaklamani, G; Chen, J; Dong, H; Stamboulis, A [School of Metallurgy and Materials, College of Engineering and Physical Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom); Mehrban, N; Bowen, J; Grover, L, E-mail: a.stamboulis@bham.ac.u [School of Chemical Engineering, College of Engineering and Physical Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom)

    2010-10-01

    In this paper active screen plasma nitriding (ASPN) is used to chemically modify the surface of UHMWPE. This is an unexplored and new area of research. ASPN allows the homogeneous treatment of any shape or surface at low temperature; therefore, it was thought that ASPN would be an effective technique to modify organic polymer surfaces. ASPN experiments were carried out at 120 {sup 0}C using a dc plasma nitriding unit with a 25% N{sub 2} and 75% H{sub 2} atmosphere at 2.5 mbar of pressure. UHMWPE samples treated for different time periods were characterized by nanoindentation, FTIR, XPS, interferometry and SEM. A 3T3 fibroblast cell line was used for in vitro cell culture experiments. Nanoindentation of UHMWPE showed that hardness and elastic modulus increased with ASPN treatment compared to the untreated material. FTIR spectra did not show significant differences between the untreated and treated samples; however, some changes were observed at 30 min of treatment in the range of 1500-1700 cm{sup -1} associated mainly with the presence of N-H groups. XPS studies showed that nitrogen was present on the surface and its amount increased with treatment time. Interferometry showed that no significant changes were observed on the surfaces after the treatment. Finally, cell culture experiments and SEM showed that fibroblasts attached and proliferated to a greater extent on the plasma-treated surfaces leading to the conclusion that ASPN surface treatment can potentially significantly improve the biocompatibility behaviour of polymeric materials.

  20. The impact of surface chemistry modification on macrophage polarisation.

    Science.gov (United States)

    Rostam, Hassan M; Singh, Sonali; Salazar, Fabian; Magennis, Peter; Hook, Andrew; Singh, Taranjit; Vrana, Nihal E; Alexander, Morgan R; Ghaemmaghami, Amir M

    2016-11-01

    Macrophages are innate immune cells that have a central role in combating infection and maintaining tissue homeostasis. They exhibit remarkable plasticity in response to environmental cues. At either end of a broad activation spectrum are pro-inflammatory (M1) and anti-inflammatory (M2) macrophages with distinct functional and phenotypical characteristics. Macrophages also play a crucial role in orchestrating immune responses to biomaterials used in the fabrication of implantable devices and drug delivery systems. To assess the impact of different surface chemistries on macrophage polarisation, human monocytes were cultured for 6 days on untreated hydrophobic polystyrene (PS) and hydrophilic O2 plasma-etched polystyrene (O2-PS40) surfaces. Our data clearly show that monocytes cultured on the hydrophilic O2-PS40 surface are polarised towards an M1-like phenotype, as evidenced by significantly higher expression of the pro-inflammatory transcription factors STAT1 and IRF5. By comparison, monocytes cultured on the hydrophobic PS surface exhibited an M2-like phenotype with high expression of mannose receptor (MR) and production of the anti-inflammatory cytokines IL-10 and CCL18. While the molecular basis of such different patterns of cell differentiation is yet to be fully elucidated, we hypothesise that it is due to the adsorption of different biomolecules on these surface chemistries. Indeed our surface characterisation data show quantitative and qualitative differences between the protein layers on the O2-PS40 surface compared to PS surface which could be responsible for the observed differential macrophage polarisation on each surface.

  1. Polymer surface modification and characterization of particulate calcium carbonate fillers

    Energy Technology Data Exchange (ETDEWEB)

    Shui Miao

    2003-12-30

    The efficacy of the surface treatment of particulate fillers depends on the chemical character of the components, on the method and conditions of the treatment, and on the amount of the treating agent. Here, the ultra-fine calcium carbonate is surface treated with 1, 2, 3 and 4 wt.% polyacrylic acid (PAA) synthesized by ourselves, which has strong ionic interaction and is an efficient surface modifier. The PAA coated filler is submitted to the measurement of the surface bonded amount, bonding efficacy, X-ray photoelectron spectroscopy (XPS) and inverse gas chromatography. Maximum efficacy is expected at the monolayer coverage of the surface, which is about 0.6 wt.% according to the calculation based on the way they are aligned and is basically in agreement with the 'substrate overlayer' model based on the mole ratio of C{sup 286} and C{sup 290} taking no account of the possible underestimation because of the inaccuracy or because of the CH{sub x} contamination present originally on the CaCO{sub 3}. The initial decrease of the mole ratio of C{sup 290}/O and C{sup 290}/Ca with the surface bonded PAA may indicate that the bonding interaction between the polymer and the filler surface is the leaving of one molecular carbon dioxide. The IGC measurement shows that there is a considerable surface tension falling in the case of the PAA modified filler compared with the reference. An abnormal high surface energy in the case of filler treated with 4% PAA is observed.

  2. Enhanced photocatalytic activity of TiO2 by surface fluorination in degradation of organic cationic compound

    Institute of Scientific and Technical Information of China (English)

    YANG Shi-ying; CHEN You-yuan; ZHENG Jian-guo; CUI Ying-jie

    2007-01-01

    Experiments were carried out to investigate the influence of TiO2 surface fluorination on the photodegradation of a representative organic cationic compound, Methylene Blue (MB). The electropositive MB shows poor adsorption on TiO2 surface; its degradation performs a HO· radical-mediated mechanism. In the F-modified system, the kinetic reaction rate enlarged more than 2.5 fold that was attributed mainly to the accumulating adsorption of MB and the increased photogenerated hole available on the F-modified TiO2 surface.

  3. Surface modification of magnesium hydroxide sulfate hydrate whiskers using a silane coupling agent by dry process

    Science.gov (United States)

    Zhu, Donghai; Nai, Xueying; Lan, Shengjie; Bian, Shaoju; Liu, Xin; Li, Wu

    2016-12-01

    In order to improve the compatibility of magnesium hydroxide sulfate hydrate (MHSH) whiskers with polymers, the surface of MHSH whiskers was modified using vinyltriethoxysilane (VTES) by dry process. The possible mechanism of the surface modification and the interfacial interactions between MHSH whiskers and VTES, as well as the effect of surface modification, were studied. Scanning electronic microscopy (SEM), transmission electron microscopy (TEM) and X-ray powder diffraction (XRD) analyses showed that the agglomerations were effectively separated and a thin layer was formed on the surface of the whiskers after modification. Fourier transform infrared (FT-IR) spectroscopy and X-ray photoelectron spectroscopy (XPS) analyses showed that the VTES molecules were bound to the surface of MHSH whiskers after modification. Chemical bonds (Sisbnd Osbnd Mg) were formed by the reaction between Sisbnd OC2H5 or Sisbnd OH and the hydroxyl group of MHSH whiskers. The effect of surface modification was evaluated by sedimentation tests, contact angle measurements and thermogravimetric analysis (TGA). The results showed that the surface of MHSH whiskers was transformed from hydrophilic to hydrophobic, and the dispersibility and the compatibility of MHSH whiskers were significantly improved in the organic phase. Additionally, the thermal stability of the VTES-modified MHSH whiskers was improved significantly.

  4. Surface Modification of Fire-retardant Asphalt with Silane Coupling Agent

    Institute of Scientific and Technical Information of China (English)

    CHEN Huiqiang; TANG Boming

    2012-01-01

    The theory and approach of the surface modified of asphalt fire-retardant with silane coupling agent were introduced,The optimum silane dosage was determined,and the structure and properties of the asphalt fire-retardant before and after the surface modification were characterized by infrared spectrum and thermo gravimetric analysis.The dispersion effect of asphalt fire-retardant was studied.The influence of the surface modification on the hydrophilicity and lipophilicity of the asphalt fire-retardant was analyzed.The experimental results showed that there were physical and chemical interactions between the silane coupling agent and the asphalt fire-retardant,which reduced the surface polarity of the asphalt fire retardant.The optimum silane coupling agent dosage was 0.95% of the asphalt fire retardant.The surface modification improved the thermal stability,dispersibility and lipophilicity of the asphalt fire retardant,which enhanced the compatibility between asphalt fire retardant and asphalt.

  5. Laser and chemical surface modifications of titanium grade 2 for medical application

    Energy Technology Data Exchange (ETDEWEB)

    Kwaśniak, P. [Faculty of Materials Science and Engineering, Warsaw University of Technology, Warsaw (Poland); Pura, J., E-mail: jaroslawpura@gmail.com [Faculty of Materials Science and Engineering, Warsaw University of Technology, Warsaw (Poland); Zwolińska, M.; Wieciński, P. [Faculty of Materials Science and Engineering, Warsaw University of Technology, Warsaw (Poland); Skarżyński, H.; Olszewski, L. [Institute of Physiology and Pathology of Hearing, Warsaw (Poland); World Hearing Center, Kajetany (Poland); Marczak, J. [Military University of Technology, Institute of Optoelectronics, Warsaw (Poland); Garbacz, H.; Kurzydłowski, K.J. [Faculty of Materials Science and Engineering, Warsaw University of Technology, Warsaw (Poland)

    2015-05-01

    Highlights: • DLIL technique and etching were used for functionalization of Ti grade 2 surface. • Modification was performed on semi-finished flat and curved Ti surfaces. • Modification results in periodic multimodal (micro and nano-size) Ti topography. - Abstract: The article presents combined, chemical and physical approach to titanium surface functionalization designed for biomedical applications. The topography modification has been obtained by employing the double laser beam interference technique and chemical etching. In the outcome, clean and smooth Ti surface as well as periodic striated topography with the roughness range from nano- to micrometers were created. The obtained structures were characterized in terms of shape, roughness, chemical composition, mechanical properties and microstructures. In order to achieve all information, numerous of research methods have been used: scanning electron microscopy, atomic force microscopy, optical profilometry and microhardness measurements. Demonstrated methodology can be used as an effective tool for manufacturing controlled surface structures improving the bone–implants interactions.

  6. Study on the mechanism of surface modification of magnesium oxysulfate whisker

    Science.gov (United States)

    Dang, Li; Nai, Xueying; Zhu, Donghai; Jing, Yanwei; Liu, Xin; Dong, Yaping; Li, Wu

    2014-10-01

    Hydrophobic-lipophilic magnesium oxysulfate whisker (MOSw) was prepared by surface modification with lauric acid and the surface morphology of MOSw was examined with field emission scanning electron microscope (FESEM). X-ray powder diffraction (XRD) was used to characterize the crystalline degree of MOSw and modified MOSw (MOSw-LA). Both FESEM and XRD suggested that modification occurred on the surface of MOSw exclusively. The inexistence of physisorbed lauric acid was proved by Fouier transform infrared (FT-IR) spectroscopy. Thermogravimetric analyses ruled out the possibility that magnesium laurate (LA-Mg) physisorbed on the surface of MOSw-LA. Solid state 13C nuclear magnetic resonance (13C NMR) further verified the formation of COO-Mglauric acid was chemical adsorption taken place between lauric acid and Mgacid-base neutralization". This research provides a detailed explanation for a kind of surface modification, which may be further used in the performance of whisker/polymer matrix composites.

  7. Enhancing the formation and shear resistance of nitrifying biofilms on membranes by surface modification

    DEFF Research Database (Denmark)

    Lackner, Susanne; Holmberg, Maria; Terada, Akihiko;

    2009-01-01

    Polypropylene (PP) membranes and polyethylene (PE) surfaces were modified to enhance formation and shear resistance of nitrifying biofilms for wastewater treatment applications. A combination of plasma polymerization and wet chemistry was employed to ultimately introduce poly(ethyleneglycol) (PEG...... similar trends: biofilms on -PEG-NH2 modified surfaces were much stronger compared to the other modifications and the unmodified reference surfaces. Electrostatic interactions between the protonated amino group and negatively charged bacteria as well as PEG chain density which can affect the surface...... structure might be possible explanations of the superiority of the -PEG-NH2 modification. The success of the-PEG-NH2 modification was independent of the original surface and might, therefore, be used in wastewater treatment bioreactors to improve reactor performance by making biofilm formation more stable...

  8. Surface modification of UHMWPE with infrared femtosecond laser

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez-Pradas, J.M., E-mail: jmfernandez@ub.edu [Departament de Fisica Aplicada i Optica, Universitat de Barcelona Marti i Franques 1, E-08028 Barcelona (Spain); Naranjo-Leon, S.; Morenza, J.L.; Serra, P. [Departament de Fisica Aplicada i Optica, Universitat de Barcelona Marti i Franques 1, E-08028 Barcelona (Spain)

    2012-09-15

    Highlights: Black-Right-Pointing-Pointer Ultra High Molecular Weight Polyethylene surface was modified with femtosecond laser pulses at 1027 nm wavelength. Black-Right-Pointing-Pointer Surface roughness is increased. Black-Right-Pointing-Pointer Ablation efficiency is maximum for 6 {mu}J pulses. Black-Right-Pointing-Pointer Irradiated surfaces remain almost chemically unaltered. - Abstract: Ultra-high-molecular-weight polyethylene (UHMWPE) is a polymer with mechanical and corrosion properties, which make it appropriate for using in biomedical devices such as hip and knee prostheses. The surface morphology and chemistry of UHMWPE influence its biocompatibility. A laser with wavelength at 1027 nm delivering 450 fs pulses at a repetition rate of 1 kHz is used to modify the surface of UHMWPE samples with 0.45 {mu}m root mean square surface roughness. Micrometric resolution is achieved with the use of a focusing lens of 0.25 NA and pulse energies of few microjoules. The study focuses in the influence of different pulse energies and pulse overlaps on the laser-induced surface roughness and ablation yield. Confocal microscopy is used to characterize changes in the morphology of the irradiated surfaces, and their chemical structure is analyzed by attenuated total reflectance infrared and Raman spectroscopies. The roughness increases as the pulse energy increases until it reaches a maximum. The ablation yield increases with the pulse energy and pulse overlap. However, the ablation yield per pulse is lower for higher pulse overlap. Pulses of 6 {mu}J have the highest ablation efficiency. Infrared and Raman spectra of samples irradiated with low energy pulses are similar to those of the pristine sample. However, some C=C and C=O bonds can be detected after irradiation with the highest pulse energies.

  9. Surface modification of pure titanium by pulsed electron beam

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, X.D. [Key Laboratory of Materials Modification and School of Materials Science and Engineering, Dalian University of Technology, Dalian 116024 (China); Laboratoired' Etude des Microstructures et de Mecanique des Materiaux (LEM3), CNRS UMR 7239, Universite Paul Verlaine - Metz, Ile du Saulcy, 57045 Metz (France); Hao, S.Z., E-mail: ebeam@dlut.edu.cn [Key Laboratory of Materials Modification and School of Materials Science and Engineering, Dalian University of Technology, Dalian 116024 (China); Li, X.N. [Key Laboratory of Materials Modification and School of Materials Science and Engineering, Dalian University of Technology, Dalian 116024 (China); Dong, C., E-mail: dong@dlut.edu.cn [Key Laboratory of Materials Modification and School of Materials Science and Engineering, Dalian University of Technology, Dalian 116024 (China); Grosdidier, T., E-mail: Thierry.grosdidier@univ-metz.fr [Laboratoired' Etude des Microstructures et de Mecanique des Materiaux (LEM3), CNRS UMR 7239, Universite Paul Verlaine - Metz, Ile du Saulcy, 57045 Metz (France)

    2011-04-15

    The microstructure, hardness and corrosion resistance of commercially pure Ti treated by low energy high current pulsed electron beam (LEHCPEB) have been investigated. The thin near-surface melted layer rapidly solidified into {beta} and subsequently transformed into ultrafine {alpha}' martensite. This has led to a drastic improvement of the corrosion properties and a significant increase (more than 60%) in hardness of the top surface.

  10. Synthesis, chemical modification, and surface assembly of carbon nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Amma, A.; St. Angelo, S.K.; Mallouk, T.E. [Department of Chemistry, The Pennsylvania State University, University Park, PA 16802 (United States); Razavi, B.; Mayer, T.S. [Electrical Engineering, The Pennsylvania State University, University Park, PA 16802 (United States)

    2003-05-01

    Carbon nanotubules and nanowires were synthesized by pyrolysis of polymer precursors in the pores of alumina membranes. The nanowires were released by dissolving the membranes, and were then made hydrophobic or hydrophilic by chemical surface derivatization. These nanowires could be placed into lithographically defined wells on surfaces by means of electrostatic interactions with monolayers at the bottoms of the wells. (Abstract Copyright [2003], Wiley Periodicals, Inc.)

  11. Laser surface modification of 316L stainless steel.

    Science.gov (United States)

    Balla, Vamsi Krishna; Dey, Sangeetha; Muthuchamy, Adiyen A; Janaki Ram, G D; Das, Mitun; Bandyopadhyay, Amit

    2017-02-28

    Medical grade 316L stainless steel was laser surface melted (LSM) using continuous wave Nd-YAG laser in argon atmosphere at 1 and 5 mm/s. The treated surfaces were characterized using electron backscatter diffraction to study the influence of top surface crystallographic orientation and type of grain boundaries on corrosion resistance, wettability, and biocompatibility. The laser scan velocity was found to have a marginal influence on the surface roughness and the type of grain boundaries. However, the crystal orientation density was found to be relatively high in 1 mm/s samples. The LSM samples showed a higher concentration of {101} and {123} planes parallel to the sample surface as well as a higher fraction of low-angle grain boundaries. The LSM samples were found to exhibit better surface wettability and enhanced the viability and proliferation of human fetal osteoblast cells in vitro when compared to the untreated samples. Further, the corrosion protection efficiency of 316L stainless steel was improved up to 70% by LSM in as-processed condition. The increased concentration of {101} and {123} planes on surfaces of LSM samples increases their surface energy, which is believed to be responsible for the improved in vitro cell proliferation. Further, the increased lattice spacing of these planes and high concentration of low-energy grain boundaries in LSM samples would have contributed to the better in vitro corrosion resistance than untreated 316L stainless steel. Our results indicate that LSM can be a potential treatment option for 316L stainless steel-based biomedical devices to improve biocompatibility and corrosion resistance. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2017.

  12. Surface modification of titanium carbide with carbyne-containing nanocoatings.

    Science.gov (United States)

    Demyashev, G M; Taube, A L; Siores, E

    2002-04-01

    The aim of this research is to investigate a novel approach to surface engineering of biomaterials that are based on transition metals of the groups IVA-VIA. The approach taken relies on the fact that, during the electropolishing of TiC surfaces, the removal of Ti atoms from the TiC surface surpasses that of C atoms. This leads to enrichment of the TiC surface with carbon. Transmission electron microscopic investigation showed that carbon-based films contain carbynes in the form of nanorod-like clusters with lengths in the range of 5-100 nm. This carbyne-containing layer is 50-100 nm thick. It was generalized that carbyne-containing nanofilms are formed on the carbide surface of transition metals of groups IVA-VIA during electropolishing. Since carbynes, being one-dimensional chain-like structures [(-C identical to C-)n/(=C=C=)n] with sp1 carbon-carbon hybridization, have the highest degree of biocompatibility because of their biological activity, the development of such surface bioengineering with carbynes extends applications of biomaterials based on transition metals of the groups IVA-VIA.

  13. Surface Modification by Atmospheric Pressure Plasma for Improved Bonding

    Science.gov (United States)

    Williams, Thomas Scott

    An atmospheric pressure plasma source operating at temperatures below 150?C and fed with 1.0-3.0 volume% oxygen in helium was used to activate the surfaces of the native oxide on silicon, carbon-fiber reinforced epoxy composite, stainless steel type 410, and aluminum alloy 2024. Helium and oxygen were passed through the plasma source, whereby ionization occurred and ˜10 16 cm-3 oxygen atoms, ˜1015 cm -3 ozone molecules and ˜1016 cm-3 metastable oxygen molecules (O21Deltag) were generated. The plasma afterglow was directed onto the substrate material located 4 mm downstream. Surface properties of the plasma treated materials have been investigated using water contact angle (WCA), atomic force microscopy (AFM), infrared spectroscopy (IR), and x-ray photoelectron spectroscopy (XPS). The work presented herein establishes atmospheric-pressure plasma as a surface preparation technique that is well suited for surface activation and enhanced adhesive bond strength in a variety of materials. Atmospheric plasma activation presents an environmentally friendly alternative to wet chemical and abrasive methods of surface preparation. Attenuated total internal reflection infrared spectroscopy was used to study the aging mechanism of the native oxide on silicon. During storage at ambient conditions, the water contact angle of a clean surface increased from composite, stainless steel type 410, and aluminum alloy 2024 was demonstrated with the atmospheric pressure helium-oxygen plasma. All surfaces studied were converted from a hydrophobic state with a water contact angle of 65° to 80° into a hydrophilic state with a water contact angle between 20° and 40° within 5 seconds of plasma exposure. X-ray photoelectron spectroscopy confirmed that the carbon atoms on the carbon-fiber/epoxy composite were oxidized, yielding 17 atom% carboxylic acid groups, 10% ketones or aldehydes and 9% alcohols. Analysis of stainless steel and aluminum by XPS illustrate oxidation of the metal

  14. Effects of Weak Surface Modification on Co/SiO2 Catalyst for Fischer-Tropsch Reaction.

    Directory of Open Access Journals (Sweden)

    Wensheng Ning

    Full Text Available A weak surface modification is applied to Co/SiO2 catalyst by hydrothermal treatment at 180°C for 5 h. Aluminum is introduced to Co/SiO2 catalysts during the surface modification. The effects of surface modification on Co/SiO2 catalyst are studied by changing the operating sequences of surface modification and cobalt impregnation in the catalyst preparation. Surface modification before cobalt impregnation makes Co3O4 particle small and dispersed into the deep part of enlarged pore in SiO2, while surface modification after cobalt impregnation does not obviously change the particle size of Co3O4. The improved amplitude of catalytic activity is similar for the two kinds of catalysts, but they are benefited from different factors. The content of iso-hydrocarbons in the products is increased by the surface modifications.

  15. Atomic and molecular layer deposition for surface modification

    Energy Technology Data Exchange (ETDEWEB)

    Vähä-Nissi, Mika, E-mail: mika.vaha-nissi@vtt.fi [VTT Technical Research Centre of Finland, PO Box 1000, FI‐02044 VTT (Finland); Sievänen, Jenni; Salo, Erkki; Heikkilä, Pirjo; Kenttä, Eija [VTT Technical Research Centre of Finland, PO Box 1000, FI‐02044 VTT (Finland); Johansson, Leena-Sisko, E-mail: leena-sisko.johansson@aalto.fi [Aalto University, School of Chemical Technology, Department of Forest Products Technology, PO Box 16100, FI‐00076 AALTO (Finland); Koskinen, Jorma T.; Harlin, Ali [VTT Technical Research Centre of Finland, PO Box 1000, FI‐02044 VTT (Finland)

    2014-06-01

    Atomic and molecular layer deposition (ALD and MLD, respectively) techniques are based on repeated cycles of gas–solid surface reactions. A partial monolayer of atoms or molecules is deposited to the surface during a single deposition cycle, enabling tailored film composition in principle down to molecular resolution on ideal surfaces. Typically ALD/MLD has been used for applications where uniform and pinhole free thin film is a necessity even on 3D surfaces. However, thin – even non-uniform – atomic and molecular deposited layers can also be used to tailor the surface characteristics of different non-ideal substrates. For example, print quality of inkjet printing on polymer films and penetration of water into porous nonwovens can be adjusted with low-temperature deposited metal oxide. In addition, adhesion of extrusion coated biopolymer to inorganic oxides can be improved with a hybrid layer based on lactic acid. - Graphical abstract: Print quality of a polylactide film surface modified with atomic layer deposition prior to inkjet printing (360 dpi) with an aqueous ink. Number of printed dots illustrated as a function of 0, 5, 15 and 25 deposition cycles of trimethylaluminum and water. - Highlights: • ALD/MLD can be used to adjust surface characteristics of films and fiber materials. • Hydrophobicity after few deposition cycles of Al{sub 2}O{sub 3} due to e.g. complex formation. • Same effect on cellulosic fabrics observed with low temperature deposited TiO{sub 2}. • Different film growth and oxidation potential with different precursors. • Hybrid layer on inorganic layer can be used to improve adhesion of polymer melt.

  16. Surface Modification Using Photo-Crosslinkable Random Copolymers

    Science.gov (United States)

    Bae, Joonwon; Bang, Joona; Lowenhielm, Peter; Spiessberger, Christian; Russell, Thomas P.; Hawker, Craig J.

    2006-03-01

    We recently reported that poly(styrene-r-methyl methacrylate) (PS-r-PMMA) random copolymers containing benzocyclobutene (BCB) group can be used to modify the surface effectively by thermal crosslinking. It was demonstrated that this method is simple, rapid, and robust, and can be applied to various surfaces. However, it requires the large amount of heat for processing, and the BCB monomer itself involves a hard chemistry. An alternative way that can replace BCB with easier chemistry and lower cost, if possible, is highly desirable. We introduce the new functional group, azide group, which can be crosslinked simply by UV irradiation, for this purpose. PS-r-PMMA random copolymers, containing various amounts of azide groups, were synthesized via controlled living-radical polymerization. It was demonstrated that even after 1 minute of the UV irradiation can crosslink the materials effectively, so that they can be used as crosslinked random copolymer mat to control the surface energy. However, it was observed that the longer irradiation time causes the damages on the surface due to the other side reactions. Depending on the UV intensity, the UV irradiation time, and the amount of azide group, the effective processing window that leads to the crosslinking without any surface damages was optimized.

  17. Surface complexation of heavy metal cations on clay edges: insights from first principles molecular dynamics simulation of Ni(II)

    Science.gov (United States)

    Zhang, Chi; Liu, Xiandong; Lu, Xiancai; He, Mengjia; Jan Meijer, Evert; Wang, Rucheng

    2017-04-01

    Aiming at an atomistic mechanism of heavy metal cation complexing on clay surfaces, we carried out systematic first principles molecular dynamics (FPMD) simulations to investigate the structures, free energies and acidity constants of Ni(II) complexes formed on edge surfaces of 2:1 phyllosilicates. Three representative complexes were studied, including monodentate complex on the tbnd SiO site, bidentate complex on the tbnd Al(OH)2 site, and tetradentate complex on the octahedral vacancy where Ni(II) fits well into the lattice. The complexes structures were characterized in detail. Computed free energy values indicate that the tetradentate complex is significantly more stable than the other two. The calculated acidity constants indicate that the tetradentate complex can get deprotonated (pKa = 8.4) at the ambient conditions whereas the other two hardly deprotonate due to extremely high pKa values. By comparing with the 2 Site Protolysis Non Electrostatic Surface Complexation and Cation Exchange (2SPNE SC/CE) model, the vacant site has been assigned to the strong site and the other two to the weak site, respectively. Thus a link has been built between atomistic simulations and macroscopic experiments and it is deduced that this should also apply to other heavy metal cations based on additional simulations of Co(II) and Cu(II) and previous simulations of Fe(II) and Cd(II)). This study forms a physical basis for understanding the transport and fixation of heavy metal elements in many geologic environments.

  18. Surface Modification of Ceramic Materials Using Excimer Laser

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Changes of surface morphology following XeCl excimer laser irradiation were investigated for three engineering ceramic materials (Al2O3, Al2O3-SiC nanocomposite and Si3N4). Al2O3 and Al2O3-SiC nanocomposite samples exhibit a smooth rapid melt layer on the surface, and the formation of the metastable γ-Al2O3 was observed. A silicon-rich layer on the surface was formed after laser irradiation of Si3N4. The toughness K1c of the materials was measured by the indentation fracture method. After laser irradiation, the toughness of Al2O3, Al2O3-SiC nanocomposite and Si3N4 was improved to various degrees: Al2O3-SiC nanocomposite, 60% (max.); Al2O3, 40% (max.); Si3N4, 12% (max.).

  19. Surface Modification of a MCFC Anode by Electrochemical Alloying

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    Considering the properties of the valve metal alloys with specific corrosion resistance and electrocatalytic ac tivity, an investigation was made to examine if nickel-niobium alloy could serve as the anode material for molten carbo nate fuel cell (MCFC). An attempt was made to produce nickel-niobium surface alloy by an electrochemical process in the molten fluorides and to testify its performance required by the MCFC anode. Experimental results indicated that the corrosion resistance as well as polarization performance of the nickel electrode was improved by the surface alloying.As far as the corrosion resistance and polarization performance is concerned, the nickel-niobium surface alloy can be considered as a candidate material for the anode of MCFC.

  20. Surface Modification of Polyethylene by Heparin for Improvement of Antithrombogenicity

    Institute of Scientific and Technical Information of China (English)

    ZHAO Guowei; CHEN Yashao; DONG Tao; WANG Xiaoli

    2007-01-01

    The purpose of this paper was to enhance blood compatibility of polyethylene (PE)film.PE film pretreated by argon plasma was subjected to ultraviolet (UV) -induced graft polymerization with Acrylic acid(AAc) (AAc-grafted PE films,PE-g-PAAc) without photo-initiator,then heparin was covalently immobilized on the PE surface (PE-g-HPAAc).The surface properties and microstructure of PE-g-PAAc and PE-g-HPAAc were studied by static contact angle measurement,atomic force microscope (AFM),X-ray photoelectron spectroscopy (XPS) and Attenuated total reflectance Fourier transfer infrared spectroscopy (ATR-FTIR).It was confirmed that AAc and heparin were successfully immobilized onto the surface of PE film.Results of platelet adhesion experiments indicated that the antithrombogenicity of the modified PE film was remarkably improved.

  1. Biomolecular modification of zirconia surfaces for enhanced biocompatibility

    Energy Technology Data Exchange (ETDEWEB)

    Hsu, Shih-Kuang; Hsu, Hsueh-Chuan [Department of Dental Technology and Materials Science, Central Taiwan University of Science and Technology, Taichung 40601, Taiwan, ROC (China); Ho, Wen-Fu [Department of Chemical and Materials Engineering, National University of Kaohsiung, Taiwan, ROC (China); Yao, Chun-Hsu [Department of Biomedical Imaging and Radiological Science, China Medical University, Taichung 40402, Taiwan, ROC (China); Chang, Pai-Ling [Taoyuan General Hospital, Taoyuan 33004, Taiwan, ROC (China); Wu, Shih-Ching, E-mail: scwu@ctust.edu.tw [Department of Dental Technology and Materials Science, Central Taiwan University of Science and Technology, Taichung 40601, Taiwan, ROC (China)

    2014-12-01

    Yttria-tetragonal zirconia polycrystal (Y-TZP) is a preferred biomaterial due to its good mechanical properties. In order to improve the biocompatibility of zirconia, RGD-peptide derived from extracellular matrix proteins was employed to modify the surface of Y-TZP to promote cell adhesion in this study. The surface of Y-TZP specimens was first modified using a hydrothermal method for different lengths of time. The topographies of modified Y-TZP specimens were analyzed by contact angle, XRD, FTIR, AFM, and FE-SEM. The mechanical properties were evaluated using Vickers hardness and three point bending strength. Then, the RGD-peptide was immobilized on the surface of the Y-TZP by chemical treatment. These RGD-peptide immobilized Y-TZP specimens were characterized by FTIR and AFM, and then were cocultured with MG-63 osteoblast cells for biocompatibility assay. The cell morphology and proliferation were evaluated by SEM, WST-1, and ALP activity assay. The XRD results indicated that the phase transition, from tetragonal phase to monoclinic phase, was increased with a longer incubation time of hydrothermal treatment. However, there were no significant differences in mechanical strengths after RGD-peptide was successfully grafted onto the Y-TZP surface. The SEM images showed that the MG-63 cells appeared polygonal, spindle-shaped, and attached on the RGD-peptide immobilized Y-TZP. The proliferation and cellular activities of MG-63 cells on the RGD-peptide immobilized Y-TZP were better than that on the unmodified Y-TZP. From the above results, the RGD-peptide can be successfully grafted onto the hydrothermal modified Y-TZP surface. The RGD-peptide immobilized Y-TZP can increase cell adhesion, and thus, improve the biocompatibility of Y-TZP. - Highlights: • Covalent bonding between peptide and Y-TZP was proposed. • Stable biomimetic structures produced on the surface of zirconia. • The biocompatibility was improved.

  2. Laser surface modification of Ti implants to improve osseointegration

    Energy Technology Data Exchange (ETDEWEB)

    Marticorena, M [Laboratorio de Ablacion Laser, Facultad de Ingenieria, Universidad de Buenos Aires, Paseo Colon 850, 1063 Buenos Aires (Argentina); Corti, G [Laboratorio de Ablacion Laser, Facultad de Ingenieria, Universidad de Buenos Aires, Paseo Colon 850, 1063 Buenos Aires (Argentina); Olmedo, D [Catedra de Anatomia Patologica, Facultad de Odontologia, Universidad de Buenos Aires. Marcelo T. de Alvear 2142, 2 piso Sector ' A' , 1122 Buenos Aires (Argentina); Guglielmotti, M B [Catedra de Anatomia Patologica, Facultad de Odontologia, Universidad de Buenos Aires. Marcelo T. de Alvear 2142, 2 piso Sector ' A' , 1122 Buenos Aires (Argentina); Duhalde, S [Laboratorio de Ablacion Laser, Facultad de Ingenieria, Universidad de Buenos Aires, Paseo Colon 850, 1063 Buenos Aires (Argentina)

    2007-04-15

    Commercially Pure Titanium foils, were irradiated using a pulsed Nd:YAG laser under ambient air, in order to produce and characterize a well controlled surface texture (roughness and waviness) that enhances osseointegration. To study the 'peri-implant' reparative process response, the laser treated Ti foils were implanted in the tibia of 10 male Wistar rats. At 14 days post-implantation, the histological analysis showed a tendency to more bone formation compared to the untreated control implants. The formation of a layer of TiN on the surface and the obtained roughness, have been demonstrated to improve bone response.

  3. Crack path and fracture surface modifications in cement composites

    Directory of Open Access Journals (Sweden)

    Sajjad Ahmad

    2015-10-01

    Full Text Available There is a tremendous increase in the use of high strength and high performance self-consolidating cementitious composites due to their superior workability and mechanical strengths. Cement composites are quasi-brittle in nature and possess extremely low tensile strength as compared to their compressive strength. Due to the low tensile strength capacity, cracks develop in cementitious composites due to the drying shrinkage, plastic settlements and/or stress concentrations (due to external restrains and/or applied stresses etc. These cracks developed at the nanoscale may grow rapidly due to the applied stresses and join together to form micro and macro cracks. The growth of cracks from nanoscale to micro and macro scale is very rapid and may lead to sudden failure of the cement composites. The present paper reports the modifications in the crack growth pattern of the high performance cement composites to achieve enhanced ductility and toughness. The objective was accomplished by the incorporation of the micro sized inert particulates in the cement composite matrix. The results indicate that the incorporation of micro sized inert particles acted as the obstacles in the growth of the cracks thus improving the ductility and the energy absorption capacity of the self-consolidating cementitious composites.

  4. Biomimetic surface modification of polypropylene by surface chain transfer reaction based on mussel-inspired adhesion technology and thiol chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Niu, Zhijun; Zhao, Yang; Sun, Wei; Shi, Suqing, E-mail: shisq@nwu.edu.cn; Gong, Yongkuan

    2016-11-15

    Highlights: • Biomimetic surface modification of PP was successfully conducted by integrating mussel-inspired technology, thiol chemistry and cell outer membranes-like structures. • The resultant biomimetic surface exhibits good interface and surface stability. • The obvious suppression of protein adsorption and platelet adhesion is also achieved. • The residue thoil groups on the surface could be further functionalized. - Abstract: Biomimetic surface modification of polypropylene (PP) is conducted by surface chain transfer reaction based on the mussel-inspired versatile adhesion technology and thiol chemistry, using 2-methacryloyloxyethylphosphorylcholine (MPC) as a hydrophilic monomer mimicking the cell outer membrane structure and 2,2-azobisisobutyronitrile (AIBN) as initiator in ethanol. A layer of polydopamine (PDA) is firstly deposited onto PP surface, which not only offers good interfacial adhesion with PP, but also supplies secondary reaction sites (-NH{sub 2}) to covalently anchor thiol groups onto PP surface. Then the radical chain transfer to surface-bonded thiol groups and surface re-initiated polymerization of MPC lead to the formation of a thin layer of polymer brush (PMPC) with cell outer membrane mimetic structure on PP surface. X-ray photoelectron spectrophotometer (XPS), atomic force microscopy (AFM) and water contact angle measurements are used to characterize the PP surfaces before and after modification. The protein adsorption and platelet adhesion experiments are also employed to evaluate the interactions of PP surface with biomolecules. The results show that PMPC is successfully grafted onto PP surface. In comparison with bare PP, the resultant PP-PMPC surface exhibits greatly improved protein and platelet resistance performance, which is the contribution of both increased surface hydrophilicity and zwitterionic structure. More importantly, the residue thiol groups on PP-PMPC surface create a new pathway to further functionalize such

  5. On-line monitoring of poly dimethylsiloxane surface modification using the photothermal deflection technique

    Energy Technology Data Exchange (ETDEWEB)

    Najmoddin, Najmeh, E-mail: najmoddin@iust.ac.ir; Khosroshahi, Mohammad E.

    2015-02-21

    Over the last decade, there has been particular interest in surface modification of biomaterials with regard to understanding the importance of surface characterization. This paper reports the use of photothermal deflection (PTD) technique to monitor modifications in poly dimethylsiloxane (PDMS) surface induced following laser treatments. The FTIR results are in agreement with PTD results, indicating that no structural changes occurred using Argon laser up to 180 s and 200 mW at 454, 488 and 514 nm wavelengths. However, with CO{sub 2} laser some physical and chemical changes occurred which are monitored by PTD technique and proved by SEM images.

  6. Biofouling behavior and performance of forward osmosis membranes with bioinspired surface modification in osmotic membrane bioreactor.

    Science.gov (United States)

    Li, Fang; Cheng, Qianxun; Tian, Qing; Yang, Bo; Chen, Qianyuan

    2016-07-01

    Forward osmosis (FO) has received considerable interest for water and energy related applications in recent years. Biofouling behavior and performance of cellulose triacetate (CTA) forward osmosis membranes with bioinspired surface modification via polydopamine (PD) coating and poly (ethylene glycol) (PEG) grafting (PD-g-PEG) in a submerged osmotic membrane bioreactor (OMBR) were investigated in this work. The modified membranes exhibited lower flux decline than the pristine one in OMBR, confirming that the bioinspired surface modification improved the antifouling ability of the CTA FO membrane. The result showed that the decline of membrane flux related to the increase of the salinity and MLSS concentration of the mixed liquid. It was concluded that the antifouling ability of modified membranes ascribed to the change of surface morphology in addition to the improvement of membrane hydrophilicity. The bioinspired surface modifications might improve the anti-adhesion for the biopolymers and biocake.

  7. Surface charging, discharging and chemical modification at a sliding contact

    DEFF Research Database (Denmark)

    Singh, Shailendra Vikram; Kusano, Yukihiro; Morgen, Per

    2012-01-01

    -ray photoelectron spectroscopy (XPS). The experiments were performed on the disk surface of a ball-on-rotating-disk apparatus; using a glass disk and a Teflon (polytetrafluoroethylene) ball arrangement, and a polyester disks and a diamondlike carbon (DLC) coated steel ball arrangement. The capacitive probe...

  8. Atmospheric pressure plasma surface modification of carbon fibres

    DEFF Research Database (Denmark)

    Kusano, Yukihiro; Løgstrup Andersen, Tom; Michelsen, Poul

    2008-01-01

    Carbon fibres are continuously treated with dielectric barrier discharge plasma at atmospheric pressure in various gas conditions for adhesion improvement in mind. An x-ray photoelectron spectroscopic analysis indicated that oxygen is effectively introduced onto the carbon fibre surfaces by He, He...

  9. Mapping physicochemical surface modifications of flame-treated polypropylene

    Directory of Open Access Journals (Sweden)

    S. Farris

    2014-04-01

    Full Text Available The aim of this work was to investigate how the surface morphology of polypropylene (PP is influenced by the surface activation mediated by a flame obtained using a mixture of air and propane under fuel-lean (equivalence ratio φ = 0.98 conditions. Morphological changes observed on flamed samples with smooth (S, medium (M, and high (H degree of surface roughness were attributed to the combined effect of a chemical mechanism (agglomeration and ordering of partially oxidized intermediate-molecular-weight material with a physical mechanism (flattening of the original roughness by the flame’s high temperature. After two treatments, the different behavior of the samples in terms of wettability was totally reset, which made an impressive surface energy of ~43 mJ•m–2 possible, which is typical of more hydrophilic polymers (e.g., polyethylene terephthalate – PET. In particular, the polar component was increased from 1.21, 0.08, and 0.32 mJ•m–2 (untreated samples to 10.95, 11.20, and 11.17 mJ•m–2 for the flamed samples S, M, and H, respectively, an increase attributed to the insertion of polar functional groups (hydroxyl and carbonyl on the C–C backbone, as demonstrated by the X-ray photoelectron spectroscopy results.

  10. Friction Surface Modification by Nanodiamonds of Denotational Synthesis

    Science.gov (United States)

    Davidov, S. V.; Gorlenko, A. O.

    2016-04-01

    The paper deals with the technology and equipment for making a hardened antifriction surface layer of machine elements on the basis of using carbon nanomaterials in order to improve wear resistance. The paper presents the results of tribotechnical tests of pins according to standard techniques using an automated system for research.

  11. Surface modification of layered zirconium phosphate with PNIPAM.

    Science.gov (United States)

    Wang, Xuezhen; Zhao, Di; Medina, Ilse B Nava; Diaz, Agustin; Wang, Huiliang; Clearfield, Abraham; Mannan, M Sam; Cheng, Zhengdong

    2016-04-04

    A new method was reported to modify layered zirconium phosphate (ZrP) with thermoresponsive polymer PNIPAM (poly N-isopropylacrylamide). PNIPAM was proved to be covalently grafted onto ZrP. (60)Co γ-rays irradiation produced peroxide groups on the surface which, upon heating, initiated free radical polymerization and subsequent attachment of PNIPAM.

  12. Nonlinear Effects of Laser Surface Modification of Ore Minerals

    Directory of Open Access Journals (Sweden)

    N.A. Leonenko

    2015-12-01

    Full Text Available The effect of continuous laser radiation on complex ore minerals objects containing gold, not extracted by monerd methods was investigated. It was established the formation of different structural surfaces of gold, revealed general patterns of sintering and concentration of sub-micron gold.

  13. Surface parameters modification by multilayer coatings deposition for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Zykova, A [Institute of Surface Engineering, 4 Zalutinskaya Str., Kharkov (Ukraine); Safonov, V [National Science Center, Kharkov Institute of Physics and Technology, 1 Akademicheskaja Str., 61108 Kharkov (Ukraine); Virva, O; Luk' yanchenko, V [Institute of Spine and Joint Pathologies, 80 Pushkinskaya Str., 61024 Kharkov (Ukraine); Walkowich, J; Rogowska, R [Institute for Sustainable Technologies, National Research Institute, 6/10 K. Pulaskiego Str., Radom (Poland); Yakovin, S [Department of Physical Technologies, Kharkov National University, 31 Kurchatov Ave., Kharkov (Ukraine)], E-mail: zykov@bi.com.ua

    2008-05-01

    Studies are presented of the surface parameters of various multilayer coatings, namely, TiN, CrN, (Ti, Cr)N, TiN/TiC{sub 10}N{sub 90}, TiN/TiC{sub 20}N{sub 80} deposited by means of Arc-PVD on stainless steel (1H18N9), as well as of the same coatings with an additional Al{sub 2}O{sub 3} film deposited by reactive magnetron sputtering (RMS). The surface thickness, roughness and topography are estimated. Other parameters, such as the surface free energy (SFE) and fractional polarity are determined by means of the Wu and the Owens-Wendt-Rabel-Kaelble methods. Experiments are carried out on the in vitro cell/material interaction (in a fibroblasts culture) in order to determine the materials biomedical response. The results show some correlation between the surface properties and cell adhesion. The best biological response parameters (cell number, proliferation function, morphology) are obtained in the case of coatings with the highest values of the polar part component of the SFE and the fractional polarity, such as TiN, TiN/TiC{sub 10}N{sub 90} and oxide coatings.

  14. Local solid-state modification of nanopore surface charges

    CERN Document Server

    Kox, Ronald; Chen, Chang; Arjmandi, Nima; Lagae, Liesbet; Borghs, Gustaaf; 10.1088/0957-4484/21/33/335703

    2012-01-01

    The last decade, nanopores have emerged as a new and interesting tool for the study of biological macromolecules like proteins and DNA. While biological pores, especially alpha-hemolysin, have been promising for the detection of DNA, their poor chemical stability limits their use. For this reason, researchers are trying to mimic their behaviour using more stable, solid-state nanopores. The most successful tools to fabricate such nanopores use high energy electron or ions beams to drill or reshape holes in very thin membranes. While the resolution of these methods can be very good, they require tools that are not commonly available and tend to damage and charge the nanopore surface. In this work, we show nanopores that have been fabricated using standard micromachning techniques together with EBID, and present a simple model that is used to estimate the surface charge. The results show that EBID with a silicon oxide precursor can be used to tune the nanopore surface and that the surface charge is stable over a...

  15. Ion beam induced optical and surface modification in plasmonic nanostructures

    Energy Technology Data Exchange (ETDEWEB)

    Singh, Udai B., E-mail: udaibhansingh123@gmail.com; Gautam, Subodh K.; Kumar, Sunil; Hooda, Sonu; Ojha, Sunil; Singh, Fouran

    2016-07-15

    In present work, ion irradiation induced nanostructuring has been exploited as an efficient and effective tool for synthesis of coupled plasmonics nanostructures by using 1.2 MeV Xe ions on Au/ZnO/Au system deposited on glass substrate. The results are correlated on the basis of their optical absorption, surface morphologies and enhanced sensitivity of evolved phonon modes by using UV Visible spectroscopy, scanning electron microscopy (SEM), and Raman spectroscopy (RS), respectively. Optical absorbance spectra of plasmonic nanostructures (NSs) show a decrease in band gap, which may be ascribed to the formation of defects with ion irradiation. The surface morphology reveals the formation of percolated NSs upon ion irradiation and Rutherford backscattering spectrometry (RBS) study clearly shows the formation of multilayer system. Furthermore, RS measurements on samples are studied to understand the enhanced sensitivity of ion irradiation induced phonon mode at 573 cm{sup −1} along with other modes. As compared to pristine sample, a stronger and pronounced evolution of these phonon modes is observed with further ion irradiation, which indicates localized surface plasmon results with enhanced intensity of phonon modes of Zinc oxide (ZnO) material. Thus, such plasmonic NSs can be used as surface enhanced Raman scattering (SERS) substrates.

  16. Modification of silicon nitride surfaces with GOPES and APTES for antibody immobilization: computational and experimental studies

    Science.gov (United States)

    Dien To, Thien; Nguyen, Anh Tuan; Nhat Thanh Phan, Khoa; Thu Thi Truong, An; Doan, Tin Chanh Duc; Mau Dang, Chien

    2015-12-01

    Chemical modification of silicon nitride (SiN) surfaces by silanization has been widely studied especially with 3-(aminopropyl)triethoxysilane (APTES) and 3-(glycidyloxypropyl) dimethylethoxysilane (GOPES). However few reports performed the experimental and computational studies together. In this study, surface modification of SiN surfaces with GOPES and APTES covalently bound with glutaraldehyde (GTA) was investigated for antibody immobilization. The monoclonal anti-cytokeratin-FITC (MACF) antibody was immobilized on the modified SiN surfaces. The modified surfaces were characterized by water contact angle measurements, atomic force microscopy and fluorescence microscopy. The FITC-fluorescent label indicated the existence of MACF antibody on the SiN surfaces and the efficiency of the silanization reaction. Absorption of APTES and GOPES on the oxidized SiN surfaces was computationally modeled and calculated by Materials Studio software. The computational and experimental results showed that modification of the SiN surfaces with APTES and GTA was more effective than the modification with GOPES.

  17. [Research development of surface hydrophilicity and lubrication modification of interventional guide wire].

    Science.gov (United States)

    Zhao, Bing; Liu, Xiaohong; Yuan, Ting

    2015-01-01

    Surface lubricity is one of the important performance criteria for interventional guide wire. In this paper, a review of the methods of surface hydrophilicity and lubrication modification of interventional guide wire is presented, including their fundamental principles, effects and some relative applications. These methods all have their own advantages and disadvantages, therefore, limitations of experimental conditions need to be taken into account.

  18. Modification of platinum surfaces by spontaneous deposition: Methanol oxidation electrocatalysis

    Energy Technology Data Exchange (ETDEWEB)

    MacDonald, J.P.; Gualtieri, B.; Runga, N.; Teliz, E.; Zinola, C.F. [Fundamental Electrochemistry Laboratory, School of Sciences, Universidad de la Republica, Igua Street No. 4225, CP 11400, Montevideo (Uruguay)

    2008-12-15

    The presence of a second metal on platinum surfaces affects the performance of methanol oxidation. However, most of the electrocatalytic reactions are studied by using electrochemically deposited platinum alloys, but in the case of spontaneous deposition the situation is not so clear since the surface distribution, stability and morphology are usually not well documented. The formation of surface decorated samples on mono- and poly-crystalline platinum is followed by electrochemical and spectroscopic techniques and analysis of their performance towards methanol adsorption and oxidation compared with that on pure platinum. Pt/Sn and Pt/Ru are of special interest because of their well-known performance in methanol fuel cells. Methanol oxidation on Pt(111)/Ru, Pt(111)/Sn and Pt(111) shows that ruthenium is the only one able to promote the reaction since the simultaneous dissolution of tin occurs and competes with the process of interest. The in situ infrared spectroscopy is used to compare methanol oxidation on Pt(111)/Ru and Pt(111) in acid media using p-polarized light. The formation of bridge bound carbon monoxide is inhibited in the presence of ruthenium ad-species, whereas on Pt(111) the three adsorption configurations are observed. Linear sweep polarization curves and Tafel slopes (calculated from steady state potentiostatic plots) for methanol oxidation are compared on polycrystalline surfaces modified by tin or ruthenium at different coverages. There is almost no change in the Tafel slopes due to the presence of the foreign metal except for Pt/Ru, where a 0.09 V decade{sup -1} slope was calculated below 0.55 V due to hydroxyl adsorbates on ruthenium islands. The anodic stripping of methanol residues on the three surfaces indicates a lower amount of carbon monoxide-type adsorbates on Pt/Ru, and the simultaneous tin dissolution process leading to residues oxidation on Pt/Sn electrodes. (author)

  19. Surface modification of poly (vinyl chloride) by long-distance and direct argon RF plasma

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    This paper reports the effects of long- distance and direct argon radio frequency (RF) plasma surface treatment on polyvinyl chloride (PVC) films in terms of changes in surface wettability and surface chemistry. The surface properties are characterized by the water contact angle measurement, X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The mechanism is further analyzed and the role of all kinds of active species, e.g. electrons, ions and free radicals involved in plasma surface modification is further evaluated. Results show that the long-distance and direct RF plasma treatments modify the PVC surface in morphology and composition, and both modifications cause surface oxidation of PVC films, in the forming of functional groups enhancing polymer wettability. The effect of the long-distance argon RF plasma is more notable. This suggests that long-distance argon RF plasma could restrain the ion and electron eroding effect and enhance free radical reaction.

  20. Surface modification of ultra-high molecular weight polyethylene for joint prosthesis and sports applications

    Institute of Scientific and Technical Information of China (English)

    H.Dong

    2004-01-01

    The recent progresses in the surfaee modification of ultra high molecular weight polyethylene (UHMWPE) using such advanced surface modification technologies as conventional ion implantation (CⅡ), new plasma immersion ion implantation (PⅢ) and novel active screen plasma (ASP), were all reported. Significantly improved wear resistance was achieved, which has great potential for extending the life-span of joint replacement prostheses and enhancing the performance of such sports equipment as skis and snowboards.

  1. PES Surface Modification Using Green Chemistry: New Generation of Antifouling Membranes.

    Science.gov (United States)

    Nady, Norhan

    2016-04-18

    A major limitation in using membrane-based separation processes is the loss of performance due to membrane fouling. This drawback can be addressed thanks to surface modification treatments. A new and promising surface modification using green chemistry has been recently investigated. This modification is carried out at room temperature and in aqueous medium using green catalyst (enzyme) and nontoxic modifier, which can be safely labelled "green surface modification". This modification can be considered as a nucleus of new generation of antifouling membranes and surfaces. In the current research, ferulic acid modifier and laccase bio-catalyst were used to make poly(ethersulfone) (PES) membrane less vulnerable to protein adsorption. The blank and modified PES membranes are evaluated based on e.g., their flux and protein repellence. Both the blank and the modified PES membranes (or laminated PES on silicon dioxide surface) are characterized using many techniques e.g., SEM, EDX, XPS and SPM, etc. The pure water flux of the most modified membranes was reduced by 10% on average relative to the blank membrane, and around a 94% reduction in protein adsorption was determined. In the conclusions section, a comparison between three modifiers-ferulic acid, and two other previously used modifiers (4-hydroxybenzoic acid and gallic acid)-is presented.

  2. Improvement of β-TCP/PLLA biodegradable material by surface modification with stearic acid.

    Science.gov (United States)

    Ma, Fengcang; Chen, Sai; Liu, Ping; Geng, Fang; Li, Wei; Liu, Xinkuan; He, Daihua; Pan, Deng

    2016-05-01

    Poly-L-lactide (PLLA) is a biodegradable polymer and used widely. Incorporation of beta tricalcium phosphate (β-TCP) into PLLA can enhance its osteoinductive properties. But the interfacial layer between β-TCP particles with PLLA matrix is easy to be destroyed due to inferior interfacial compatibility of the organic/inorganic material. In this work, a method of β-TCP surface modification with stearic acid was investigated to improve the β-TCP/PLLA biomaterial. The effects of surface modification on the β-TCP were investigated by FTIR, XPS, TGA and CA. It was found that the stearic acid reacted with β-TCP and oxhydryl was formed during the surface modification. Hydrophilicity of untreated or modified β-TCP/PLLA composite was increased by the addition of 10 wt.% β-TCP, but it decreased as the addition amount increased from 10 wt.% to 20 wt.%. Two models were suggested to describe the effect of β-TCP concentration on CA of the composites. Mechanical properties of β-TCP/PLLA composites were tested by bending and tensile tests. Fractures of the composites after mechanical test were observed by SEM. It was found that surface modification with stearic acid improved bending and tensile strengths of the β-TCP/PLLA composites obviously. The SEM results indicated that surface modification decreased the probability of interface debonding between fillers and matrix under load.

  3. Inexpensive laser-induced surface modification in bismuth thin films

    Energy Technology Data Exchange (ETDEWEB)

    Contreras, A. Reyes [Facultad de Ciencias, Universidad Autónoma del Estado de México, Carretera Toluca, Ixtlahuaca Kilómetro 15.5, C.P. 50200 Edo. de México (Mexico); Hautefeuille, M., E-mail: mathieu_h@ciencias.unam.mx [Facultad de Ciencias, Universidad Nacional Autónoma de México, Avenida Universidad 3000, Circuito Exterior S/N, Coyoacán, Ciudad Universitaria, C.P. 04510 D.F. Mexico (Mexico); García, A. Esparza [Fotofísica y Películas Delgadas, Departamento de Tecnociencias, CCADET-UNAM, Circuito exterior s/n C.P. 04510 Cd. Universitaria, D.F. Mexico (Mexico); Mejia, O. Olea [Centro Conjunto de Investigación en Química Sustentable UAEM-UNAM, Carretera Toluca-Atlacomulco, Km 14.5, Unidad El Rosedal, 50200 San Cayetano, Estado de México (Mexico); López, M.A. Camacho [Facultad de Química, Universidad Autónoma del Estado de México, Tollocan s/n, esq. Paseo Colón, Toluca, Estado de México 50110 (Mexico)

    2015-05-01

    Highlights: • Laser-induced microbumps were formed on bismuth films using a simple, low-cost, laser setup. • The patterns, similar to those typically obtained with high-power lasers, were characterized. • Control of laser ablation conditions is critical in the fabrication of surface microbumps. - Abstract: In this work, we present results on texturing a 500 nm thick bismuth film, deposited by sputtering onto a glass slide using a low-cost homemade, near-infrared pulsed laser platform. A 785 nm laser diode of a CD–DVD pickup head was precisely focused on the sample mounted on a motorized two-axis translation stage to generate localized surface microbumps on the bismuth films. This simple method successfully transferred desired micropatterns on the films in a computer-numerical control fashion. Irradiated zones were characterized by atomic force microscopy and scanning electron microscopy. It was observed that final results are strongly dependent on irradiation parameters.

  4. Mitigating irreversible capacity losses from carbon agents via surface modification

    Science.gov (United States)

    Molina Piper, Daniela; Son, Seoung-Bum; Travis, Jonathan J.; Lee, Younghee; Han, Sang Sub; Kim, Seul Cham; Oh, Kyu Hwan; George, Steven M.; Lee, Se-Hee; Ban, Chunmei

    2015-02-01

    Greatly improved cycling performance has been demonstrated with conformally coated lithium-ion electrodes by atomic layer deposition (ALD) and molecular layer deposition (MLD) techniques. This paper reports the impact of coating on the electrode additives towards mitigating undesired parasitic reactions during cycling. The ALD and MLD coatings with conformality and atomic scale thickness control effectively stabilize the surface of the electrode components, and the current collector, resulting in the increase of coulombic efficiency throughout cycling. The organic fragment integrated into the recently developed MLD process allows the coating to possess excellent mechanical properties and enhanced ionic conductivity, which significantly reduces cell polarizations throughout cycling. This work validates the importance of ALD and MLD as surface modifiers and further demonstrates their versatility and compatibility with lithium-ion battery technology.

  5. Surface modification of UHMWPE for use in total joint replacements.

    Science.gov (United States)

    Zhang, Min; James, Susan P; King, Richard; Beauregard, Guy

    2004-01-01

    To create a hydrophilic, lubricious, more wear-resistant UHMWPE bearing, a novel hyaluronan (HA) derivative and novel UHMWPE-hyaluronan composite were developed. HA was silylated to increase its hydrophobicity and compatibility with UHMWPE. The sily1 HA rapidly diffused into the connected pores of UHMWPE preforms in xylenes solution, and fixed within UHMWPE and on its surface after crosslinking. A micro-composite was obtained after hot-pressing the porous preform. The presence of HA film on the composite surface has been demonstrated through X-Ray photoelectron spectroscopy (XPS) analysis and Toluidine Blue O (TBO) dye assay. The aqueous contact angles of micro-composite samples were significantly lower compared with UHMWPE control samples, and the samples processed with hydrolysis prior to final molding were superior to those processed with hydrolysis after molding.

  6. Surface Modification of ZnO Nanorods with Hamilton Receptors

    Directory of Open Access Journals (Sweden)

    Lukas Zeininger

    2015-04-01

    Full Text Available A new prototype of a Hamilton receptor suitable for the functionalization of inorganic nanoparticles was synthesized and characterized. The hydrogen bonding receptor was coupled to a catechol moiety, which served as anchor group for the functionalization of metal oxides, in particular zinc oxide. Synthesized zinc oxide nanorods [ZnO] were used for surface functionalization. The wet-chemical functionalization procedure towards monolayer-grafted particles [ZnO-HR] is described and a detailed characterization study is presented. In addition, the detection of specific cyanurate molecules is demonstrated. The hybrid structures [ZnO-HR-CA] were stable towards agglomeration and exhibited enhanced dispersability in apolar solvents. This observation, in combination with several spectroscopic experiments gave evidence of the highly directional supramolecular recognition at the surface of nanoparticles.

  7. The effect of polymer surface modification on polymer-protein interaction via interfacial polymerization and hydrophilic polymer grafting

    Science.gov (United States)

    Protein membrane separation is prone to fouling on the membrane surface resulting from protein adsorption onto the surface. Surface modification of synthetic membranes is one way to reduce fouling. We investigated surface modification of polyethersulfone (PES) as a way of improving hydrophilicity ...

  8. Modification of the dentin surface by using carbon nanotubes.

    OpenAIRE

    Akasaka, Tsukasa; Nakata, Keiko; Uo, Motohiro; WATARI, Fumio

    2009-01-01

    Recent studies have shown that carbon nanotubes (CNTs) can be used as biomedical materials because of their unique properties. CNTs effect nucleation of hydroxyapatite, because of which considerable interest has been generated regarding the use of CNTs in dentistry. However, there are only a few reports on the use of CNTs as dental materials. In this study, we investigated the changes induced in the surfaces of tooth slices by the application of a coating of CNTs by observing CNT-coated tooth...

  9. Modification of Fluoropolymer Surfaces with Electronically Conductive Polymers

    Science.gov (United States)

    1993-06-01

    CI0 4)3. Polyaniline was synthesized by mixing equal volumes of a solution that was 0.25 M in ammonium persulfate and a solution that was 0.5 M in...31 Conductive polymers, polypyrrole , lithography 16. PRICE CODE 17. SECURITY CLASSIFICATION 18. SECURITY CLASSIFICATION 19. SECURITY CLASSIFICATION...surface. Fortunately, conductive polymers such as polypyrrole adhere quite well to many substrates, including nylon, polycarbonate, cellulosics

  10. Synthesis and Surface Modification of CdTe Nanocrystals

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    CdTe nanocrystals were prepared in aqueous solution via the reaction between Cd2+ and NaHTe in the presence of mercaptoacetic acid. Interactions between CdTe nanocrystals and phenylalanine were formed via electrostatic/coordinate self-assembly. The photoluminescence intensity of CdTe nanocrystals was improved obviously. The interaction mechanism was discussed and was considered to be surface passivation.

  11. Electronic structure tuning via surface modification in semimetallic nanowires

    Science.gov (United States)

    Sanchez-Soares, Alfonso; O'Donnell, Conor; Greer, James C.

    2016-12-01

    Electronic structure properties of nanowires (NWs) with diameters of 1.5 and 3 nm based on semimetallic α -Sn are investigated by employing density functional theory and perturbative GW methods. We explore the dependence of electron affinity, band structure, and band-gap values with crystallographic orientation, NW cross-sectional size, and surface passivants of varying electronegativity. We consider four chemical terminations in our study: methyl (CH3), hydrogen (H ), hydroxyl (OH ), and fluorine (F ). Results suggest a high degree of elasticity of Sn-Sn bonds within the Sn NWs' cores with no significant structural variations for nanowires with different surface passivants. Direct band gaps at Brillouin-zone centers are found for most studied structures with quasiparticle corrected band-gap magnitudes ranging from 0.25 to 3.54 eV in 1.5-nm-diameter structures, indicating an exceptional range of properties for semimetal NWs below the semimetal-to-semiconductor transition. Band-gap variations induced by changes in surface passivants indicate the possibility of realizing semimetal-semiconductor interfaces in NWs with constant cross-section and crystallographic orientation, allowing the design of novel dopant-free NW-based electronic devices.

  12. Biomimetic surface modification of polyurethane with phospholipids grafted carbon nanotubes.

    Science.gov (United States)

    Tan, Dongsheng; Liu, Liuxu; Li, Zhen; Fu, Qiang

    2015-08-01

    To improve blood compatibility of polyurethane (PU), phospholipids grafted carbon nanotubes (CNTs) were prepared through zwitterion-mediated cycloaddition reaction and amide condensation, and then were added to the PU as fillers via solution mixing to form biomimetic surface. The properties of phospholipids grafted CNTs (CNT-PC) were investigated by thermal gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and proton nuclear magnetic resonance ((1) H NMR). The results indicated that the phospholipids were grafted onto CNTs in high efficiency, and the hydrophilicity and dispersibility of the modified CNTs were improved effectively. The structures and properties of composites containing CNT-PC were investigated by optical microscope, XPS, and water contact angles. The results indicated that phospholipids were enriched on the surface with addition of 0.1 wt % of CNT-PC, which significantly reduced protein adsorption and platelet adhesion. The method of carrying phospholipids on the nanofiller to modify polymers has provided a promising way of constructing biomimetic phospholipid membrane on the surface to improve blood compatibility.

  13. Modification of the dentin surface by using carbon nanotubes.

    Science.gov (United States)

    Akasaka, Tsukasa; Nakata, Keiko; Uo, Motohiro; Watari, Fumio

    2009-01-01

    Recent studies have shown that carbon nanotubes (CNTs) can be used as biomedical materials because of their unique properties. CNTs effect nucleation of hydroxyapatite, because of which considerable interest has been generated regarding the use of CNTs in dentistry. However, there are only a few reports on the use of CNTs as dental materials. In this study, we investigated the changes induced in the surfaces of tooth slices by the application of a coating of CNTs by observing CNT-coated tooth slices both macroscopically as well as under a scanning electron microscope. Further, we investigated the effect of CNT coating on the tensile bond strength of dentin adhesives. CNTs adhered easily to the tooth surfaces when tooth slices were suspended in a CNT-dispersed solution. Interestingly, it was observed that CNTs selectively adhered to the surfaces of dentin and cementum, possibly by adhering to their exposed collagen fibers. In addition, the CNT coating did not affect the tensile bond strength of dentin adhesives. These results indicate that coating of the teeth with CNTs can be a possible application of CNTs as dental materials.

  14. Chemical surface modification of porous silicon with palladium and characterizations

    Energy Technology Data Exchange (ETDEWEB)

    Kanungo, J.; Maji, S.; Saha, H. [IC Design and Fabrication Centre, Department of Electronics and Telecommunication Engineering, Jadavpur University, Kolkata 700032 (India); Basu, S., E-mail: sukumar_basu@yahoo.co.u [IC Design and Fabrication Centre, Department of Electronics and Telecommunication Engineering, Jadavpur University, Kolkata 700032 (India)

    2010-03-15

    Porous silicon (PS) was formed on p-type crystalline silicon of (1 0 0) orientation and 2-5 OMEGA cm resistivity by the electrochemical anodization method using HF and ethanol as the electrolyte. Adjusting the current density and the HF concentration in the electrolyte the porosity of the samples were varied from 40% to 60%. The porous silicon surface was modified with PdCl{sub 2} solution by a low cost chemical method. Both the unmodified and the modified PS were thoroughly characterized by the EDAX analysis, the digital X-ray image mapping and the XPS study. Electrical characteristics were performed by the I-V measurements for both the lateral and the sandwich structures using Al metal contact. The I-V characteristics of the modified PS for all the porosity were more reproducible compared to the unmodified PS surfaces. It was further observed that the conductivity increased with the increasing porosity for the Pd-modified surfaces whereas it decreased for the unmodified PS.

  15. Surface modification of nanoporous alumina membranes by plasma polymerization.

    Science.gov (United States)

    Losic, Dusan; Cole, Martin A; Dollmann, Björn; Vasilev, Krasimir; Griesser, Hans J

    2008-06-18

    The deposition of plasma polymer coatings onto porous alumina (PA) membranes was investigated with the aim of adjusting the surface chemistry and the pore size of the membranes. PA membranes from commercial sources with a range of pore diameters (20, 100 and 200 nm) were used and modified by plasma polymerization using n-heptylamine (HA) monomer, which resulted in a chemically reactive polymer surface with amino groups. Heptylamine plasma polymer (HAPP) layers with a thickness less than the pore diameter do not span the pores but reduce their diameter. Accordingly, by adjusting the deposition time and thus the thickness of the plasma polymer coating, it is feasible to produce any desired pore diameter. The structural and chemical properties of modified membranes were studied by scanning electron microscopy (SEM), atomic force microscopy (AFM) and x-ray electron spectroscopy (XPS). The resultant PA membranes with specific surface chemistry and controlled pore size are applicable for molecular separation, cell culture, bioreactors, biosensing, drug delivery, and engineering complex composite membranes.

  16. SURFACE MODIFICATION OF POLYPROPYLENE MICROPOROUS MEMBRANE BY TETHERING POLYPEPTIDES

    Institute of Scientific and Technical Information of China (English)

    Zhen-mei Liu; Zhi-kang Xu; Mathias Ulbricht

    2006-01-01

    Two kinds of polypeptides were tethered onto the surface of polypropylene microporous membrane (PPMM)through a ring opening polymerization of L-glutamate N-carboxyanhydride initiated by amino groups which were introduced by ammonia plasma and γ-aminopropyl triethanoxysilane treatments. X-ray photoelectron spectroscopy (XPS), attenuated total reflectance Fourier transform infrared spectroscopy (FT-IR/ATR), scanning electron microscopy (SEM), together with water contact angle measurements were used to characterize the modified membranes. XPS analyses and FT-IR/ATR spectra demonstrated that polypeptides are actually grafted onto the membrane surface. The wettability of the membrane surface increases at first and then decreases with the increase in grafting degrees of polypeptide. Platelet adhesion and murine macrophage attachment experiments reveal an enhanced hemocompatibility for the polypeptide modified PPMMs. All these results give evidence that polypeptide grafting can simultaneously improve the hemocompatibility as well as reserve the hydrophobicity for the membrane, which will provide a potential approach to improve the performance of polypropylene hollow fiber microporous membrane used in artificial oxygenator.

  17. Gaseous phase coal surface modification. Final technical report

    Energy Technology Data Exchange (ETDEWEB)

    Okoh, J.M.; Pinion, J.; Thiensatit, S.

    1992-05-07

    In this report, we present an improved, feasible and potentially cost effective method of cleaning and beneficiating ultrafine coal. Increased mechanization of mining methods and the need towards depyritization, and demineralization have led to an increase in the quantity of coal fines generated in recent times. For example, the amount of {minus}100 mesh coal occurring in coal preparation plant feeds now typically varies from 5 to 25% of the total feed. Environmental constraints coupled with the greatly increased cost of coal have made it increasingly important to recover more of these fines. Our method chemically modifies the surface of such coals by a series of gaseous phase treatments employing Friedel-Crafts reactions. By using olefins (ethene, propene and butene) and hydrogen chloride catalyst at elevated temperature, the surface hydrophobicity of coal is enhanced. This increased hydrophobicity is manifest in surface phenomena which reflect conditions at the solid/liquid interphase (zeta potential) and those which reflect conditions at the solid/liquid/gas interphases (contact angle, wettability and floatability).

  18. Biomimetic surface modification of polypropylene by surface chain transfer reaction based on mussel-inspired adhesion technology and thiol chemistry

    Science.gov (United States)

    Niu, Zhijun; Zhao, Yang; Sun, Wei; Shi, Suqing; Gong, Yongkuan

    2016-11-01

    Biomimetic surface modification of polypropylene (PP) is conducted by surface chain transfer reaction based on the mussel-inspired versatile adhesion technology and thiol chemistry, using 2-methacryloyloxyethylphosphorylcholine (MPC) as a hydrophilic monomer mimicking the cell outer membrane structure and 2,2-azobisisobutyronitrile (AIBN) as initiator in ethanol. A layer of polydopamine (PDA) is firstly deposited onto PP surface, which not only offers good interfacial adhesion with PP, but also supplies secondary reaction sites (-NH2) to covalently anchor thiol groups onto PP surface. Then the radical chain transfer to surface-bonded thiol groups and surface re-initiated polymerization of MPC lead to the formation of a thin layer of polymer brush (PMPC) with cell outer membrane mimetic structure on PP surface. X-ray photoelectron spectrophotometer (XPS), atomic force microscopy (AFM) and water contact angle measurements are used to characterize the PP surfaces before and after modification. The protein adsorption and platelet adhesion experiments are also employed to evaluate the interactions of PP surface with biomolecules. The results show that PMPC is successfully grafted onto PP surface. In comparison with bare PP, the resultant PP-PMPC surface exhibits greatly improved protein and platelet resistance performance, which is the contribution of both increased surface hydrophilicity and zwitterionic structure. More importantly, the residue thiol groups on PP-PMPC surface create a new pathway to further functionalize such zwitterion modified PP surface.

  19. Plasma Surface Modification of Polyaramid Fibers for Protective Clothing

    Science.gov (United States)

    Widodo, Mohamad

    2011-12-01

    The purpose of this research was to develop a novel process that would achieve biocidal properties on Kevlar fabric via atmospheric pressure plasma jet (APPJ) induced-graft polymerization of monomers. In the course of the study, experiments were carried out to understand plasma-monomer-substrate interactions, particularly, how each of the main parameters in the plasma processing affects the formation of surface radicals and eventually the degree of graft polymerization of monomers. The study also served to explore the possibility of developing plasma-initiated and plasma-controlled graft polymerization for continuous operation. In this regards, three methods of processing were studied, which included two-step plasma graft-polymerization with immersion, two-step and one-step plasma graft-polymerization with pad-dry. In general, plasma treatment did not cause visible damage to the surface of Kevlar fibers, except for the appearance of tiny globules distributed almost uniformly indicating a minor effect of plasma treatment to the surface morphology of the polymer. From the examination of SEM images, however, it was found that a very localized surface etching seemed to have taken place, especially at high RF power (800 W) and long time of exposure (60 s), even in plasma downstream mode of operation. It was suggested that a small amount of charged particles might have escaped and reached the substrate surface. High density of surface radicals, which is the prerequisite for high graft density and high antimicrobial activity, was achieved by the combination of high RF power and short exposure time or low RF power and long time of exposure. This was a clear indication that the formation of surface radicals is a function of amount of the dissipated energy, which also explained the two-factor interaction between the two process parameters. XPS results showed that hydrolysis of the anilide bond of PPTA chains took place to some extent on the surface of Kevlar, leading to the

  20. Nanoscale surface modifications to control capillary flow characteristics in PMMA microfluidic devices

    Directory of Open Access Journals (Sweden)

    Mukhopadhyay Subhadeep

    2011-01-01

    Full Text Available Abstract Polymethylmethacrylate (PMMA microfluidic devices have been fabricated using a hot embossing technique to incorporate micro-pillar features on the bottom wall of the device which when combined with either a plasma treatment or the coating of a diamond-like carbon (DLC film presents a range of surface modification profiles. Experimental results presented in detail the surface modifications in the form of distinct changes in the static water contact angle across a range from 44.3 to 81.2 when compared to pristine PMMA surfaces. Additionally, capillary flow of water (dyed to aid visualization through the microfluidic devices was recorded and analyzed to provide comparison data between filling time of a microfluidic chamber and surface modification characteristics, including the effects of surface energy and surface roughness on the microfluidic flow. We have experimentally demonstrated that fluid flow and thus filling time for the microfluidic device was significantly faster for the device with surface modifications that resulted in a lower static contact angle, and also that the incorporation of micro-pillars into a fluidic device increases the filling time when compared to comparative devices.

  1. Ion beam modification of surfaces for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Sommerfeld, Jana

    2014-07-15

    Human life expectancy increased significantly within the last century. Hence, medical care must ever be improved. Optimizing artificial replacements such as hip joints or stents etc. is of special interest. For this purpose, new materials are constantly developed or known ones modified. This work focused on the possibility to change the chemistry and topography of biomedically relevant materials such as diamond-like carbon (DLC) and titanium dioxide (TiO{sub 2}) by means of ion beam irradiation. Mass-separated ion beam deposition was used in order to synthesize DLC layers with a high sp{sup 3} content (> 70%), a sufficiently smooth surface (RMS<1 nm) and a manageable film thickness (50 nm). The chemistry of the DLC layers was changed by ion beam doping with different ion species (Ag,Ti) and concentrations. Additionally, the surface topography of silicon and titanium dioxide was altered by ion beam irradiation under non-perpendicular angle of incidence. The created periodic wave structures (so-called ripples) were characterized and their dependency on the ion energy was investigated. Moreover, ripples on silicon were covered with a thin DLC layer in order to create DLC ripples. The biocompatibility of all samples was investigated by adsorption experiments. For this purpose, human plasma fibrinogen (HPF) was used due to its ambiphilic character, which allows the protein to assume different conformations on materials with different hydrophilicities. Moreover, HPF is a crucial factor in the blood coagulation process. This work comes to the conclusion that the interaction of both, the surface chemistry and topography, has a strong influence on the adsorption behavior of HPF and thus the biocompatibility of a material. Both factors can be specifically tuned by means of ion beam irradiation.

  2. STUDY OF SURFACE MODIFIED POLYMERS IN THE MODIFICATION OF NANOMATERIALS

    Directory of Open Access Journals (Sweden)

    G. V. Popov

    2014-01-01

    Full Text Available The comparative study of change of surface tension of solutions of some commercial rubbers before and after thermal ageing technique du-Nui, analyzed the features of change of surface tension of solutions of various rubbers in the presence of a mixture of fullerenes. Calculations of the Gibbs energy and the analysis of the obtained data to predict the behavior of polymer systems when changes are made to mix of fullerenes in a wide concentration range. When comparing the results of changes in Gibbs energy and the surface tension in fluids rubbers shown that mentioned above in solutions of elastomers aged, than the control. This fact confirms the initial chapeau of physic-chemical interactions of molecules fullerenes by segments of the Kuna and end groups of the polymer chains, as it is known that when thermal-oxidative degradation of rubbers, respectively the number of segments of the Kuna and branched loose ends of macromolecules that are free to react with fullerenes in solution, free from spatial constraints. A comparative analysis of the interaction of rubbers with different chemical composition with double branches has shown that it is easier to just react and has minimum energy polibutadien interaction that has to do with lack of branching and no radicals in its structure and in the backbone chain. The maximum energy of interaction with Fullerenes have SBS rubber because it has large styrene blocks in the main polymer chain that causes the spatial constraints to direct contact with fullerene molecules, you can assume that the interaction is only low-molecular fraction of Fullerenes mixture, possessing the necessary dimensions. As a result of the study shows that the application of the method of separation ring (Du-Nui allows you to predict the properties of rubber with modified nanomaterial’s with minimal labor costs.

  3. Surface modification of poly(L-lactic acid) with biomolecules to promote endothelialization.

    Science.gov (United States)

    Xia, Yun; Boey, Freddy; Venkatraman, Subbu S

    2010-09-01

    Rapid endothelialization is important for biodegradable blood-contacting devices not only to prevent thrombosis but also to prevent degradation debris from entering the bloodstream and causing further complications. Here the authors report a three-step surface modification method, by which biomolecules, such as gelatin and chitosan, are covalently immobilized on the surface of plasma-treated poly(L-lactic acid) (PLLA) via -COOH groups introduced by acrylic acid grafting polymerization. Surface characterization techniques, including x-ray photoelectron spectroscopy, contact angle measurement, and colorimetric methods for surface density of functional groups, proved the feasibility and stability of this surface modification method. Surface wettability was increased by biomolecules immobilization. The -COOH surface density was measured to be 4.17±0.15 μmol/cm(2), the and amount of gelatin immobilized was 4.8 μg/cm(2). Human umbilical vein endothelial cell was used during in vitro study at seeding density of 10(4) cells/cm(2). PLLA-gAA-gelatin surface was found to enhance cell adhesion, spreading, focal adhesion formation, and proliferation significantly. Chitosan-modified PLLA shows marginally improvement in cell adhesion and proliferation. Endothelialization was achieved within 7 days on both modified PLLA surfaces. In conclusion, this work demonstrates the feasibility of the surface modification method, and its ability to promote complete endothelialization for cardiovascular applications.

  4. Surface property modification of coatings via self-stratification

    Science.gov (United States)

    Pieper, Robert Joseph

    Biological fouling occurs everywhere in the marine environment and is a significant problem for marine vessels. Anti-fouling coatings have been used effectively to prevent fouling; however, these coatings harm non-targeted sea-life. Fouling-release coatings (FRC) appear to be an alternative way to combat fouling. FRC do not necessarily prevent the settlement of marine organisms but rather allow their easy removal with application of shear to the coatings surface. These coatings must be non-toxic, non-leaching, have low surface energy, low modulus, and durability to provide easy removal of marine organisms. Here the goal is to develop FRC based on thermosetting siloxane-polyurethane, amphiphilic polyurethane, and zwitterionic/amphiphilic polyurethane systems. A combinatorial high-throughput approach has been taken in order to explore the variables that may affect the performance of the final coatings. Libraries of acrylic polyols were synthesized using combinatorial high-throughput techniques by either batch or semi-batch processes. The design of the experiments for the batch and semi-batch processes were done combinatorially to explore a range of compositions and various reaction process variables that cannot be accomplished or are not suitable for single reaction experiments. Characterization of Rapid-GPC, high-throughput DSC, and gravimetrically calculated percent solids verified the effects of different reaction conditions on the MW, glass transition temperatures, and percent conversion of the different compositions of acrylic polyols. Coatings were characterized for their surface energy, pseudobarnacle pull-off adhesion, and were subjected to bioassays including marine bacteria, algae, and barnacles. From the performance properties results the acrylic polyol containing 20% hydroxyethyl acrylate and 80% butyl acrylate was selected for further siloxane-polyurethane formulations and were subjected to the same physical, mechanical, and performance testing

  5. Organic synthesis - applications in enzymatic studies, catalysis and surface modification

    DEFF Research Database (Denmark)

    Viart, Helene Marie-France

    as liposomes and the enzymatic activity was studied. Hydrolysis (or absence of hydrolysis) was monitored by MALDI-TOF-MS. The results observedin these experiments are compared to MD predictions and confirm them. The second chapter deals with surface functionalization of liposomes. The copper mediated [3...... and a functionality covalently linked to a coupling partner (such as small molecule, peptide, etc.), we investigated the efficiency of the reaction depending on the position of the functional groups (whether on the liposome or on the coupling partner). Our results indicate that the reaction is most efficient when...

  6. Ultrasound enhanced plasma surface modification at atmospheric pressure

    DEFF Research Database (Denmark)

    Kusano, Yukihiro; Singh, Shailendra Vikram; Norrman, Kion

    2012-01-01

    Efficiency of atmospheric pressure plasma treatment can be highly enhanced by simultaneous high power ultrasonic irradiation onto the treating surface. It is because ultrasonic waves with a sound pressure level (SPL) above ∼140 dB can reduce the thickness of a boundary gas layer between the plasma...... arc at atmospheric pressure to study adhesion improvement. The effect of ultrasonic irradiation with the frequency diapason between 20 and 40 kHz at the SPL of ∼150 dB was investigated. After the plasma treatment without ultrasonic irradiation, the wettability was significantly improved...

  7. Surface modification of investment cast-316L implants: microstructure effects.

    Science.gov (United States)

    El-Hadad, Shimaa; Khalifa, Waleed; Nofal, Adel

    2015-03-01

    Artificial femur stem of 316L stainless steel was fabricated by investment casting using vacuum induction melting. Different surface treatments: mechanical polishing, thermal oxidation and immersion in alkaline solution were applied. Thicker hydroxyapatite (HAP) layer was formed in the furnace-oxidized samples as compared to the mechanically polished ones. The alkaline treatment enhanced the precipitation of HAP on the samples. It was also observed that the HAP precipitation responded differently to the different phases of the microstructure. The austenite phase was observed to have more homogeneous and smoother layer of HAP. In addition, the growth of HAP was sometimes favored on the austenite phase rather than on ferrite phase.

  8. A Chemical-Adsorption Strategy to Enhance the Reaction Kinetics of Lithium-Rich Layered Cathodes via Double-Shell Surface Modification.

    Science.gov (United States)

    Guo, Lichao; Li, Jiajun; Cao, Tingting; Wang, Huayu; Zhao, Naiqin; He, Fang; Shi, Chunsheng; He, Chunnian; Liu, Enzuo

    2016-09-21

    Sluggish surface reaction kinetics hinders the power density of Li-ion battery. Thus, various surface modification techniques have been applied to enhance the electronic/ionic transfer kinetics. However, it is challenging to obtain a continuous and uniform surface modification layer on the prime particles with structure integration at the interface. Instead of classic physical-adsorption/deposition techniques, we propose a novel chemical-adsorption strategy to synthesize double-shell modified lithium-rich layered cathodes with enhanced mass transfer kinetics. On the basis of experimental measurement and first-principles calculation, MoO2S2 ions are proved to joint the layered phase via chemical bonding. Specifically, the Mo-O or Mo-S bonds can flexibly rotate to bond with the cations in the layered phase, leading to the good compatibility between the thiomolybdate adsorption layer and layered cathode. Followed by annealing treatment, the lithium-excess-spinel inner shell forms under the thiomolybdate adsorption layer and functions as favorable pathways for lithium and electron. Meanwhile, the nanothick MoO3-x(SO4)x outer shell protects the transition metal from dissolution and restrains electrolyte decomposition. The double-shell modified sample delivers an enhanced discharge capacity almost twice as much as that of the unmodified one at 1 A g(-1) after 100 cycles, demonstrating the superiority of the surface modification based on chemical adsorption.

  9. Effect of Surface Modification on Microbiol Polyhydroxyalkanoate Films on Biocompatibility

    Institute of Scientific and Technical Information of China (English)

    杨霰霜; 赵锴; 陈金春; 夏彩虹; 陈国强

    2001-01-01

    The purpose of this study was to investigate in vitro biocompatibility of a new type of polymer, polyhydroxybutyrate-co-hexanoate (PHBHHx). The hydrophilicity and biocompatibility were studied with two kinds of enzymes, amylase BAN480L and lipase Novozym388. The degree of hydrophilicity was observed using contact angle measurements. In vitro biocompatibility evaluations were carried out by direct incubation of mouse fibroblast cell line L929 on the polyhydroxyalkanoate (PHA) films. The samples treated with BAN480L showed that the PHA biocompatibility increased while the hydrophilicity decreased. Relative to untreated samples, the number of cells on the Novozym388 modified PHBHHx significant decrease as the hydrophilicity also decreased. The results indicated that other surface characteristics besides hydrophilicity influence the biocompatibility of PHBHHx films.

  10. Surface modification of commercial tin coatings by carbon ion implantation

    Energy Technology Data Exchange (ETDEWEB)

    Liu, L.J.; Sood, D.K.; Manory, R.R. [Royal Melbourne Inst. of Tech., VIC (Australia)

    1993-12-31

    Commercial TiN coatings of about 2 {mu}m thickness on high speed steel substrates were implanted at room temperature with 95 keV carbon ions at nominal doses between 1 x 10{sup 17} - 8x10{sup 17} ions cm{sup -2}. Carbon ion implantation induced a significant improvement in ultramicrohardness, friction coefficient and wear properties. The surface microhardness increases monotonically by up to 115% until a critical dose is reached. Beyond this dose the hardness decreases, but remains higher than that of unimplanted sample. A lower friction coefficient and a longer transition period towards a steady state condition were obtained by carbon ion implantation. The changes in tribomechanical properties are discussed in terms of radiation damage and possible formation of a second phase rich in carbon. 6 refs., 3 figs.

  11. Surface modification for polystyrene colloidal particles with controlled charge densities.

    Science.gov (United States)

    Lee, Jongman; Kwon, Oh-Sun; Shin, Kwanwoo; Song, Ju-Myung; Kim, Joon-Seop; Seo, Young-Soo; Tael, Giyoong; Jon, Sangyong

    2007-11-01

    A significant amount of polystyrene sulfonated acid (PSSA) and poly(styrene-ran-acrylic acid) (PSAA) random copolymer can be adsorbed by dispersion of PS particles via a swelling-quenching process. A THF-water mixed solvent was used in the swelling process and a large amount of pure water was used, to give a low concentration of THF% in quenching process. Our results showed that functional PSSA groups were randomly and tightly adsorbed to the PS particles. When the mol.% of charged segments was increased, the progressive adsorption of PSSA chains to the PS particles leads to an increase in the electrophoretic mobility and zeta-potential of aqueous dispersions. Thus, we were able to obtain well-distributed surface charge density on the PS particles.

  12. SURFACE MODIFICATION AND DISPERSION OF NANODIAMOND IN CLEAN OIL

    Institute of Scientific and Technical Information of China (English)

    Yongwei Zhu; Xiangyang Xu; Baichun Wang; Zhijing Feng

    2004-01-01

    The effect of different kinds of surfactants on the size distribution of nanodiamond particles in clean oil was studied. Results show that the dispersing stability of nanodiamond modified with surfactants YS-1 and SB-18 simultaneously is much better than those modified with either of them because of synergism of the surfactants. And the particle size distribution in the system can be improved remarkably after the adoption of hyperdispersants such as SA-E and SA-F. Anchoring groups of those hyperdispersants can be bonded with the particle surface by chemical and/or hydrogen bonding and their soluble chains are well compatible with the dispersion media. As a result, the particles are uniformly distributed in the system owing to the steric stabilization. A very stable clean-oil based nanodiamond suspension with an average particle size of around 53.2 nm was prepared.

  13. Surface modification of polymers for biocompatibility via exposure to extreme ultraviolet radiation.

    Science.gov (United States)

    Inam Ul Ahad; Bartnik, Andrzej; Fiedorowicz, Henryk; Kostecki, Jerzy; Korczyc, Barbara; Ciach, Tomasz; Brabazon, Dermot

    2014-09-01

    Polymeric biomaterials are being widely used for the treatment of various traumata, diseases and defects in human beings due to ease in their synthesis. As biomaterials have direct interaction with the extracellular environment in the biological world, biocompatibility is a topic of great significance. The introduction or enhancement of biocompatibility in certain polymers is still a challenge to overcome. Polymer biocompatibility can be controlled by surface modification. Various physical and chemical methods (e.g., chemical and plasma treatment, ion implantation, and ultraviolet irradiation etc.) are in use or being developed for the modification of polymer surfaces. However an important limitation in their employment is the alteration of bulk material. Different surface and bulk properties of biomaterials are often desirable for biomedical applications. Because extreme ultraviolet (EUV) radiation penetration is quite limited even in low density mediums, it could be possible to use it for surface modification without influencing the bulk material. This article reviews the degree of biocompatibility of different polymeric biomaterials being currently employed in various biomedical applications, the surface properties required to be modified for biocompatibility control, plasma and laser ablation based surface modification techniques, and research studies indicating possible use of EUV for enhancing biocompatibility.

  14. Surface modification of silicon-containing fluorocarbon films prepared by plasma-enhanced chemical vapor deposition

    Science.gov (United States)

    Jin, Yoonyoung; Desta, Yohannes; Goettert, Jost; Lee, G. S.; Ajmera, P. K.

    2005-07-01

    Surface modification of silicon-containing fluorocarbon (SiCF) films achieved by wet chemical treatments and through x-ray irradiation is examined. The SiCF films were prepared by plasma-enhanced chemical vapor deposition, using gas precursors of tetrafluoromethane and disilane. As-deposited SiCF film composition was analyzed by x-ray photoelectron spectroscopy. Surface modification of SiCF films utilizing n-lithiodiaminoethane wet chemical treatment is discussed. Sessile water-drop contact angle changed from 95°+/-2° before treatment to 32°+/-2° after treatment, indicating a change in the film surface characteristics from hydrophobic to hydrophilic. For x-ray irradiation on the SiCF film with a dose of 27.4 kJ/cm3, the contact angle of the sessile water drop changed from 95°+/-2° before radiation to 39°+/-3° after x-ray exposure. The effect of x-ray exposure on chemical bond structure of SiCF films is studied using Fourier transform infrared measurements. Electroless Cu deposition was performed to test the applicability of the surface modified films. The x-ray irradiation method offers a unique advantage in making possible surface modification in a localized area of high-aspect-ratio microstructures. Fabrication of a Ti-membrane x-ray mask is introduced here for selective surface modification using x-ray irradiation.

  15. Drag reduction in reservoir rock surface: Hydrophobic modification by SiO2 nanofluids

    Science.gov (United States)

    Yan, Yong-Li; Cui, Ming-Yue; Jiang, Wei-Dong; He, An-Le; Liang, Chong

    2017-02-01

    Based on the adsorption behavior of modified silica nanoparticles in the sandstone core surface, the hydrophobic surface was constructed, which consists of micro-nanoscale hierarchical structure. This modified core surface presents a property of drag reduction and meets the challenge of high injection pressure and low injection rate in low or ultra-low permeability reservoir. The modification effects on the surface of silica nanoparticles and reservoir cores, mainly concerning hydrophobicity and fine structure, were determined by measurements of contact angle and scanning electron microscopy. Experimental results indicate that after successful modification, the contact angle of silica nanoparticles varies from 19.5° to 141.7°, exhibiting remarkable hydrophobic properties. These modified hydrophobic silica nanoparticles display a good adsorption behavior at the core surface to form micro-nanobinary structure. As for the wettability of these modified core surfaces, a reversal has happened from hydrophilic into hydrophobic and its contact angle increases from 59.1° to 105.9°. The core displacement experiments show that the relative permeability for water has significantly increased by an average of 40.3% via core surface modification, with the effects of reducing injection pressure and improving injection performance of water flooding. Meanwhile, the mechanisms of drag reduction and improving water injection operation induced from the modified core surface were uncovered. The present study will establish a fundamental understanding on the drag reduction at the core surface modified by nanofluids and its applications in more industries.

  16. Study on the mechanism of surface modification of magnesium oxysulfate whisker

    Energy Technology Data Exchange (ETDEWEB)

    Dang, Li [Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Nai, Xueying; Zhu, Donghai [Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008 (China); Jing, Yanwei [Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Liu, Xin; Dong, Yaping [Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008 (China); Li, Wu, E-mail: driverlaoli@163.com [Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008 (China)

    2014-10-30

    Graphical abstract: - Highlights: • Physisorbed lauric acid was ruled out by FT-IR spectroscopy. • The inexistence of physisorbed magnesium laurate was proved by DSC analyses. • {sup 13}C NMR further verified the formation of COO–Mg< bonds on the surface of MOSw. • “Acid-base neutralization” was proved by the pH meter monitoring synchronously. • The type of surface modification of MOSw was proved to be chemical adsorption only. - Abstract: Hydrophobic-lipophilic magnesium oxysulfate whisker (MOSw) was prepared by surface modification with lauric acid and the surface morphology of MOSw was examined with field emission scanning electron microscope (FESEM). X-ray powder diffraction (XRD) was used to characterize the crystalline degree of MOSw and modified MOSw (MOSw-LA). Both FESEM and XRD suggested that modification occurred on the surface of MOSw exclusively. The inexistence of physisorbed lauric acid was proved by Fouier transform infrared (FT-IR) spectroscopy. Thermogravimetric analyses ruled out the possibility that magnesium laurate (LA-Mg) physisorbed on the surface of MOSw-LA. Solid state {sup 13}C nuclear magnetic resonance ({sup 13}C NMR) further verified the formation of COO–Mg< bonds based on the significant changes of chemical shift and decrease in intensity. Hence, we confirmed that the type of surface modification of MOSw with lauric acid was chemical adsorption taken place between lauric acid and Mg<. In order to study the dynamic state approach of this reaction, a pH meter was employed to monitor the reaction process synchronously, and then we proposed a reaction mechanism which was similar to the “acid-base neutralization”. This research provides a detailed explanation for a kind of surface modification, which may be further used in the performance of whisker/polymer matrix composites.

  17. Recent advances in synthesis and surface modification of superparamagnetic iron oxide nanoparticles with silica

    Science.gov (United States)

    Sodipo, Bashiru Kayode; Aziz, Azlan Abdul

    2016-10-01

    Research on synthesis of superparamagnetic iron oxide nanoparticles (SPION) and its surface modification for biomedical applications is of intense interest. Due to superparamagnetic property of SPION, the nanoparticles have large magnetic susceptibility, single magnetic domain and controllable magnetic behaviour. However, owing to easy agglomeration of SPION, surface modification of the magnetic particles with biocompatible materials such as silica nanoparticle has gained much attention in the last decade. In this review, we present recent advances in synthesis of SPION and various routes of producing silica coated SPION.

  18. Surface modification of graphene nanopores for protein translocation

    Science.gov (United States)

    Shan, Y. P.; Tiwari, P. B.; Krishnakumar, P.; Vlassiouk, I.; Li, W.Z.; Wang, X.W.; Darici, Y.; Lindsay, S.M.; Wang, H. D.; Smirnov, S.; He, J.

    2014-01-01

    Studies of DNA translocation through graphene nanopores have revealed their potential for DNA sequencing. Here we report a study of protein translocation through chemically modified graphene nanopores. A transmission electron microscope (TEM) was used to cut nanopores with diameters between 5-20 nm in multilayer graphene prepared by chemical vapor deposition (CVD). After oxygen plasma treatment, the dependence of the measured ionic current on salt concentration and pH was consistent with a small surface charge induced by the formation of carboxyl groups. While translocation of gold nanoparticles (10 nm) was readily detected through such treated pores of a larger diameter, translocation of protein ferritin was not observed either for oxygen plasma treated pores, or for pores modified with mercaptohexadecanoic acid. Ferritin translocation events were reliably observed after the pores were modified with the phospholipid-PEG (DPPE-PEG750) amphiphile. The ion current signature of translocation events was complex, suggesting that a series of interactions between the protein and pore occur during the process. PMID:24231385

  19. Surface modification of adamantane-terminated gold nanoclusters using cyclodextrins.

    Science.gov (United States)

    Yan, Chunyang; Liu, Chao; Abroshan, Hadi; Li, Zhimin; Qiu, Renhua; Li, Gao

    2016-08-17

    The surface functionality of Au38S2(SAdm)20 nanoclusters (-SAdm = adamantanethiolate) in the presence of α-, β-, and γ-cyclodextrins (CDs) is studied. The supramolecular chemistry and host-guest interactions of CDs and the protecting ligands of nanoclusters are investigated using UV-vis and NMR spectroscopies, MALDI mass spectrometry, and molecular dynamics simulations. In contrast to α- and γ-CDs, the results show that β-CDs are capable of efficiently chemisorbing onto the Au38S2(SAdm)20 nanoclusters to yield Au38S2(SAdm)20-(β-CD)2 conjugates. MD simulations revealed that two -SAdm ligands of the nanoparticle with the least steric hindrance are capable to selectively be accommodated into hydrophobic cavity of β-CDs, as furthermore confirmed by NMR spectroscopy. The conjugates largely improve the stability of the nanoclusters in the presence of strong oxidants (e.g., TBHP). Further, the electrochemical properties of Au38S2(SAdm)20 nanoclusters and Au38S2(SAdm)20-(β-CD)2 conjugates are compared. The charge transfer to the redox probe molecules (e.g., K3Fe(CN)6) in solution was monitored by cyclic voltammetry. It is found that β-CDs act as an umbrella to cover the fragile metal cores of the nanoclusters, thereby blocking direct interaction with destabilizing agents and hence quenching the charge transfer process.

  20. The Quest for Nonthrombotic Surface Modifications to Achieve Hemocompatibility of Implantable Devices.

    Science.gov (United States)

    Tchouta, Lise Nadine; Bonde, Pramod Narayan

    2015-01-01

    The use of blood-contacting implantable devices is limited by surface-induced thrombosis, which has led to the development of thromboresistant surfaces. Multidisciplinary efforts have promoted the development of surface modifications to minimize thrombosis by targeting surface-induced coagulation. To this date, no material has been identified that remains irrevocably hemocompatible with time but many options are now available with their own limitations. Essential to this review is the understanding of some of the challenges in this field and newer opportunities for hemocompatibility research. This report will also briefly review many of the achievements in the development of hemocompatible biomaterial coating, including surface modifications against protein adsorption and platelet adhesion, biomimetism, and endothelialization.

  1. Effect of plasticizer on surface of free films prepared from aqueous solutions of salts of cationic polymers with different plasticizers

    Science.gov (United States)

    Bajdik, János; Fehér, Máté; Pintye-Hódi, Klára

    2007-06-01

    Acquisition of a more detailed understanding of all technological processes is currently a relevant tendency in pharmaceutical technology and hence in industry. A knowledge of film formation from dispersion of polymers is very important during the coating of solid dosage forms. This process and the structure of the film can be influenced by different additives. In the present study, taste-masking films were prepared from aqueous citric acid solutions of a cationic polymer (Eudragit ® E PO) with various hydrophilic plasticizers (glycerol, propylene glycol and different poly(ethylene glycols)). The mechanical properties, film thickness, wetting properties and surface free energy of the free films were studied. The aim was to evaluate the properties of surface of free films to predict the arrangement of macromolecules in films formed from aqueous solutions of salts of cationic polymers. A high molecular weight of the plasticizer decreased the work of deformation. The surface free energy and the polarity were highest for the film without plasticizer; the hydrophilic additives decreased these parameters. The direction of the change in polarity (a hydrophilic component caused a decrease in the polarity) was unexpected. It can be explained by the change in orientation of the macromolecules, a hydrophobic surface being formed. Examination of the mechanical properties and film thickness can furnish additional results towards a knowledge of film formation by this not frequently applied type of polymer from aqueous solution.

  2. Acute in vivo toxicity mitigation of PEI-coated maghemite nanoparticles using controlled oxidation and surface modifications toward siRNA delivery.

    Science.gov (United States)

    Israel, Liron Limor; Lellouche, Emmanuel; Ostrovsky, Stella; Yarmiayev, Valeria; Bechor, Moshe; Michaeli, Shulamit; Lellouche, Jean-Paul Moshe

    2015-07-22

    A ceric ammonium nitrate (CAN)-based doping step was used for the fabrication of core maghemite nanoparticles (NPs) that enabled the obtainment of colloid particles with a view to a high-level nanoparticle (NP) surface doping by Ce(III/IV). Such doping of Ce(III/IV) cations enables one to exploit their quite rich coordination chemistry for ligand coordinative binding. In fact, they were shown to act as powerful Lewis acid centers for attaching any organic (Lewis base) ligand such as a 25 kDa branched PEI polymer. Resulting conPEI25-CAN-γ-Fe2O3 NPs have been fully characterized before a successful implementation of siRNA loading and cell delivery/gene silencing using a well-known dual luciferase system. This attractive result emphasized their significant potential as an NP platform technology toward additional MRI and/or drug delivery (peptide)-relating end applications. However, due to their high positive charge, PEI polymers can cause severe in vivo toxicity due to their interaction with negatively charged red blood cells (RBC), resulting in RBC aggregation and lysis, leading to thrombosis and, finally, to animal death. In order to mitigate these acute toxic effects, two different types of surface modifications were performed. One modification included the controlled oxidation of 0.1-5% of the PEI amines before or after conjugation to the NPs, using hydrogen peroxide or potassium persulfate. The other type of modification was the addition of a second biocompatible polyanionic polymer to the PEI grafted NPs, based on the concept of a layer-by-layer (LbL) technique. This modification is based on the coordination of another polyanionic polymer on the NPs surface in order to create a combined hybrid PEI and polyanionic polymer nanosystem. In both cases, the surface modification successfully mitigated the NP acute in vivo toxicity, without compromising the silencing efficiency.

  3. Preparing cationic cotton linter cellulose with high substitution degree by ultrasonic treatment.

    Science.gov (United States)

    Zhang, Fulong; Pang, Zhiqiang; Dong, Cuihua; Liu, Zong

    2015-11-05

    As an important cellulose derivative, cationic cellulose has becoming an attractive material. However, it remains challenging to produce cationic cellulose with high substitute degree. In this paper, we successfully increased the substitute degree of cationic cellulose by introducing ultrasonic treatment, which efficiently breaks hydrogen bonds of the chemical structure of cationic cellulose. Properties of cationic cellulose were studied by scanning electron spectroscope (SEM), contact angle, X-ray diffraction (XRD) and thermogravimetric analysis (TGA). Experimental results show that the cationic cellulose has rougher surface and lower crystallinity degree as compared to the original sample. TGA analysis verifies that the thermostability of CLC decreases after the cationic modification. The residual of the cationic cellulose (25 wt%) after pyrolysis increases significantly as compared to that of the original cellulose (15 wt%).

  4. Surface morphological modification of crosslinked hydrophilic co-polymers by nanosecond pulsed laser irradiation

    Science.gov (United States)

    Primo, Gastón A.; Alvarez Igarzabal, Cecilia I.; Pino, Gustavo A.; Ferrero, Juan C.; Rossa, Maximiliano

    2016-04-01

    This work reports an investigation of the surface modifications induced by irradiation with nanosecond laser pulses of ultraviolet and visible wavelengths on crosslinked hydrophilic co-polymeric materials, which have been functionalized with 1-vinylimidazole as a co-monomer. A comparison is made between hydrogels differing in the base co-monomer (N,N-dimethylaminoethyl methacrylate and N-[3-(dimethylamino)propyl] methacrylamide) and in hydration state (both swollen and dried states). Formation of craters is the dominant morphological change observed by ablation in the visible at 532 nm, whereas additional, less aggressive surface modifications, chiefly microfoams and roughness, are developed in the ultraviolet at 266 nm. At both irradiation wavelengths, threshold values of the incident laser fluence for the observation of the various surface modifications are determined under single-pulse laser irradiation conditions. It is shown that multiple-pulse irradiation at 266 nm with a limited number of laser shots can be used alternatively for generating a regular microfoam layer at the surface of dried hydrogels based on N,N-dimethylaminoethyl methacrylate. The observations are rationalized on the basis of currently accepted mechanisms for laser-induced polymer surface modification, with a significant contribution of the laser foaming mechanism. Prospective applications of the laser-foamed hydrogel matrices in biomolecule immobilization are suggested.

  5. Flotation separation of polyvinyl chloride and polyethylene terephthalate plastics combined with surface modification for recycling.

    Science.gov (United States)

    Wang, Chongqing; Wang, Hui; Fu, Jiangang; Zhang, Lingling; Luo, Chengcheng; Liu, Younian

    2015-11-01

    Surface modification with potassium permanganate (KMnO4) solution was developed for separation of polyvinyl chloride (PVC) and polyethylene terephthalate (PET) waste plastics. The floatability of PVC decreases with increasing of KMnO4 concentration, treatment time, temperature and stirring rate, while that of PET is unaffected. Fourier transform infrared (FT-IR) analysis confirms that mechanism of surface modification may be due to oxidization reactions occurred on PVC surface. The optimum conditions are KMnO4 concentration 1.25 mM/L, treatment time 50 min, temperature 60°C, stirring rate 300 r/min, frother concentration 17.5 g/L and flotation time 1 min. PVC and PET with different particle sizes were separated efficiently through two-stage flotation. Additionally, after ultrasonic assisted surface modification, separation of PVC and PET with different mass ratios was obtained efficiently through one-stage flotation. The purity and the recovery of the obtained products after flotation separation are up to 99.30% and 99.73%, respectively. A flotation process was designed for flotation separation of PVC and PET plastics combined with surface modification. This study provides technical insights into physical separation of plastic wastes for recycling industry.

  6. PES Surface Modification Using Green Chemistry: New Generation of Antifouling Membranes

    Directory of Open Access Journals (Sweden)

    Norhan Nady

    2016-04-01

    Full Text Available A major limitation in using membrane-based separation processes is the loss of performance due to membrane fouling. This drawback can be addressed thanks to surface modification treatments. A new and promising surface modification using green chemistry has been recently investigated. This modification is carried out at room temperature and in aqueous medium using green catalyst (enzyme and nontoxic modifier, which can be safely labelled “green surface modification”. This modification can be considered as a nucleus of new generation of antifouling membranes and surfaces. In the current research, ferulic acid modifier and laccase bio-catalyst were used to make poly(ethersulfone (PES membrane less vulnerable to protein adsorption. The blank and modified PES membranes are evaluated based on e.g., their flux and protein repellence. Both the blank and the modified PES membranes (or laminated PES on silicon dioxide surface are characterized using many techniques e.g., SEM, EDX, XPS and SPM, etc. The pure water flux of the most modified membranes was reduced by 10% on average relative to the blank membrane, and around a 94% reduction in protein adsorption was determined. In the conclusions section, a comparison between three modifiers—ferulic acid, and two other previously used modifiers (4-hydroxybenzoic acid and gallic acid—is presented.

  7. Modification and characterization of an aptamer-based surface plasmon resonance sensor chip

    Directory of Open Access Journals (Sweden)

    Tan Junpeng

    2017-01-01

    Full Text Available Recently, aptamer-based surface plasmon resonance (SPR sensors have become increasingly popular due to their high specificity, high sensitivity, real-time detection capabilities, and label-free features. The core component of an aptamer-based SPR sensor is a chip. This paper presents the modification steps and the characterization results of a sensor chip for the construction of a 2, 4, 6-trinitrotoluene-targeted, aptamer-based, SPR sensor. After cleaning the aptamer-based SPR sensor chip, polyethylene glycol (PEG with functional thiol groups at one end was added to the chip surface by Au-S covalent bonds to form a self-assembled film. Then, the carboxyl groups at the other end of PEG and the carboxyl groups of trinitrophenyl-glycine (TNP-Gly were activated and connected via ethylenediamine (EDA. This effectively completed the chip’s modification. During the modification process, relevant experimental conditions were optimized. The chip’s surface elements, as well as their chemical states, were characterized by X-ray photoelectron spectroscopy (XPS. The results, outlined in the following study, demonstrate that this modification of an aptamer-based SPR sensor chip adhered to normative expectations. Thus, the modification process proposed here establishes an important foundation for subsequent study of TNT detection.

  8. Surface modifications and Nano-composite coatings to improve the bonding strength of titanium-porcelain

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Litong, E-mail: guolitong810104@163.com [China University of Mining and Technology, Xuzhou 221116 (China); ustralian Institute for Bioengineering and Nanotechnology, The University of Queensland, Brisbane, QLD 4072 (Australia); Chen, Xiaoyuan; Liu, Xuemei; Feng, Wei [China University of Mining and Technology, Xuzhou 221116 (China); Li, Baoe [School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130 (China); Lin, Cheng; Tao, Xueyu; Qiang, Yinghuai [China University of Mining and Technology, Xuzhou 221116 (China)

    2016-04-01

    Surface modifications of Ti and nano-composite coatings were employed to simultaneously improve the surface roughness, corrosion resistance and chemical bonding between porclain-Ti. The specimens were studied by field-emission scanning electron microscopy, surface roughness, differential scanning calorimetry, Fourier transform infrared spectroscopy, corrosion resistance and bonding strength tests. The SEM results showed that hybrid structures with micro-stripes, nano-pores and nano-protuberances were prepared by surface modification of Ti, which significantly enhanced the surface roughness and corrosion resistance of Ti. Porous nano-composite coatings were synthesized on Ti anodized with pre-treatment in 40% HF acid. TiO{sub 2} nanoparticles were added into the hybrid coating to increase the solid phase content of the sols and avoid the formation of microcracks. With the TiO{sub 2} content increasing from 45 wt% to 60 wt%, the quantities of the microcracks on the coating surface gradually decreased. The optimal TiO{sub 2} content for the nanocomposite coatings is 60 wt% in this research. Compared to the uncoated group, the bonding strength of the coated groups showed a bonding strength improvement of 23.96%. The cytotoxicity of the 4# coating group was ranked as zero, which corresponds to non-cytotoxicity. - Highlights: • Surface roughness of Ti was increased by surface modification of Ti. • Corrosion resistance was enhanced by surface modification of Ti. • Porous nano-composite coatings were synthesized on Ti by sol–gel process. • TiO{sub 2} nanoparticles were added into the coating to avoid formation of cracks. • The nano-composite coatings increased the bonding strength of about 24%.

  9. Efficient improvement of surface activity of tea saponin through Gemini-like modification by straightforward esterification.

    Science.gov (United States)

    Feng, Jin; Chen, Ying; Liu, Xin; Liu, Songbai

    2015-03-15

    Novel strategy of Gemini-like modification has been applied in development of new nonionic surfactants, tea saponin esters, with enhanced surface activity by simple esterification. Tea saponin was treated with acyl chlorides of different chain length and different ratio of tea saponin and acyl chloride under alkaline condition. The structures of tea saponin esters were analysed and confirmed by FT-IR, NMR and ESI-MS. Surface activity investigation revealed that esterification with the chain length of C12 and C14 and the ratio of 1:4 to 1:6 produced superior surface activity compared with tea saponin. The exceptional surface activity of the new surfactants suggested their great potential application in food industry as green surfactants due to their environmental benign nature as well as simple and inexpensive preparation. The strategy of Gemini-like modification will facilitate development of green surfactants based on natural resources.

  10. [Surface modification of poly methyl methacrylate intraocular lens by alpha-allyl glucoside].

    Science.gov (United States)

    Qu, Chao; Yao, Ke; Kou, Ruiqiang; Xu, Zhikang

    2004-02-01

    A method for improving the biocompatibility of the intraocular lens (IOL) and reducing the cell attachment was adopted in this study. The alpha-Allyl glucoside was used for the surface modification of the poly methyl methacrylate (PMMA) IOL by way of plasma-induced in situ polymerization. The surfaces of the control and treatment IOLs were characterized by contact angle estimation and ESCA techniques. The resolution, diopter and anti-fatigue of loops were determined by physical and optical methods. Cell attachment on the surfaces was examined by light microscopy. The results indicated that all of the treatment groups had excellent physical and optical properties. The modification with the use of alpha-Allyl glucoside could improve the hydrophilicity of the anterior surface of the PMMA IOLs and reduce the cell attachment.

  11. Modification of Teflon surface by proton microbeam and nitrogen ion beam

    Energy Technology Data Exchange (ETDEWEB)

    Kitamura, Akane, E-mail: ogawa.akane@jaea.go.jp [Department of Advanced Radiation Technology, Takasaki Advanced Radiation Research Institute, Japan Atomic Energy Agency, 1233 Watanuki-machi, Takasaki, Gunma 370-1292 (Japan); Satoh, Takahiro; Koka, Masashi; Kamiya, Tomihiro [Department of Advanced Radiation Technology, Takasaki Advanced Radiation Research Institute, Japan Atomic Energy Agency, 1233 Watanuki-machi, Takasaki, Gunma 370-1292 (Japan); Kobayashi, Tomohiro [Advanced Science Institute, RIKEN, 2-1 Hirosawa, Wako-shi, Saitama 350-0198 (Japan)

    2013-11-01

    Teflon surfaces were modified using a combination of 3 MeV proton microbeam scanning and subsequent 250 keV N{sub 2}{sup +} ion beam irradiation. When a Teflon surface is irradiated using only an N{sub 2}{sup +} ion beam, micro-protrusions are densely formed in the irradiated area. It has been previously confirmed that these protrusions aid the attachment of biological cells, which then spread on the surface. Therefore, modification of the Teflon surface patterning is necessary in order to enhance its functionality as cell culture substrata. In this study, flat areas and depressed structures were created among the dense micro-protrusions by bubbles that were generated inside the sample using proton beam scanning. This modification will contribute to the fabrication of cell culture dishes with the advantages of micro-protrusions.

  12. Towards convective heat transfer enhancement: surface modification, characterization and measurement techniques

    NARCIS (Netherlands)

    Taha, T.J.; Thakur, D.B.; Meer, van der T.H.

    2012-01-01

    In this work, heat transfer surface modification and heat transfer measurement technique is developed. Heat transfer investigation was aimed to study the effect of carbon nano fibers (extremely high thermal conductive material) on the enhancement level in heat transfer. Synthesis of these carbon nan

  13. Surface Modification of a PCB Substrate for Better Adhesion of Inkjet Printed Circuit Structures

    NARCIS (Netherlands)

    Sridhar, A.; Dijk, van D.J.; Akkerman, R.

    2009-01-01

    The robustness and service life of inkjet printed electronic circuit structures are highly influenced by the state of the interface between these structures and the substrate. In the case of polymeric substrate materials, surface modification is necessary to realise a favourable interface, as these

  14. Surface modification of PDMS microchips with poly(ethylene glycol) derivatives for μTAS applications.

    Science.gov (United States)

    de Campos, Richard Piffer Soares; Yoshida, Inez Valeria Pagotto; da Silva, José Alberto Fracassi

    2014-08-01

    In this work is presented a method for the modification of native PDMS surface in order to improve its applicability as a substrate for microfluidic devices, especially in the analysis of nonpolar analytes. Therefore, poly(ethylene glycol) divinyl ether modified PDMS substrate was obtained by surface modification of native PDMS. The modified substrate was characterized by attenuated total reflectance infrared spectroscopy, water contact angle measurements, and by evaluating the adsorption of rhodamine B and the magnitude of the EOF mobility. The reaction was confirmed by the spectroscopic evaluation. The formation of a well-spread water film over the surface immediately after the modification was an indicative of the modified surface hydrophilicity. This characteristic was maintained for approximately ten days, with a gradual return to a hydrophobic state. Fluorescence assays showed that the nonpolar adsorption property of PDMS was significantly decreased. The EOF mobility obtained was 3.6 × 10(-4) cm(2) V(-1) s(-1) , higher than the typical values found for native PDMS. Due to the better wettability promoted by the modification, the filling of the microchannels with aqueous solutions was facilitated and trapping of air bubbles was not observed.

  15. SURFACE MODIFICATION OF NANOPARTICLES TO OPPOSE UPTAKE BY THE MONONUCLEAR PHAGOCYTE SYSTEM

    NARCIS (Netherlands)

    STORM, G; BELLIOT, SO; DAEMEN, T; LASIC, DD

    1995-01-01

    An overview of recent advances in the surface modification of colloidal particles to oppose uptake by the mononuclear phagocyte system (MPS) is presented. First, we describe the colloidal particles and hydrophilic coating materials investigated, with particular focus on the literature concerning par

  16. PLASMA POLYMERIZATION OF HYDROPHILIC AND HYDROPHOBIC MONOMERS FOR SURFACE MODIFICATION OF NUCLE-MICROPOROUS MEMBRANE

    Institute of Scientific and Technical Information of China (English)

    LI Xuefen; LI Zhifen; CHEN Chuanfu; WU Wenhui

    1990-01-01

    Surface modification of nucle-microporous membrane by plasma polymerization of HEMA, NVP and D4 has been studied. The hydrophilicity of membranes was increased with increasing of plasma polymerization time of hydrophilic monomers HEMA and NVP. The flow rate of water through the membrane was increased remarkably after plasma polymerization of HEMA on it.

  17. Specific surface modification of the acetylene-linked glycolipid vesicle by click chemistry.

    Science.gov (United States)

    Ito, Hidehiro; Kamachi, Toshiaki; Yashima, Eiji

    2012-06-07

    A novel glycolipid with a terminal acetylene was synthesized and used to prepare unilamellar vesicles. Using these vesicles, a convenient method was developed for the specific modification of the vesicle surface using the photoresponsive copper complex [Cu(OH(2))(cage)] as the catalyst for a click reaction.

  18. Proceedings of the 10th international symposium on polymer surface modification

    Science.gov (United States)

    Contamination of meats, seafood, poultry, eggs, and fresh and fresh-cut fruits and vegetables is an ongoing concern. Although well-established in non-food applications for surface treatment and modification, cold plasma is a relatively new food safety intervention. As a nonthermal food processing te...

  19. Effect of Water Adsorption on Cation-Surface Interaction Energy in the Na-Mordenite of 5.5 : 1 Si/Al Ratio

    Directory of Open Access Journals (Sweden)

    Sekou Diaby

    2016-01-01

    Full Text Available The mobility of the Na+ cations localized at the inner surface of the studied mordenite zeolite depends on the material surface properties. In this work, we show that the activation energy, ΔEhop, relating to the Na+ cation hopping displacement is associated to the surface potential and therefore can be used to get a better insight into the zeolite surface properties. Indeed, when molecules as water are adsorbed at the surface, they modify the surface potential energy and hence influence the value of ΔEhop. If the adsorbed molecules are polar they directly interact with the cations which become more mobile. The more the ΔEhop value is, the less the amount of adsorbed water molecules is. Alterations of the ΔEhop value with respect to the amount of adsorbed water molecules are interpreted using the Dubinin model which is based on simple adsorption principle.

  20. Surface Wettability Modification of Cyclic Olefin Polymer by Direct Femtosecond Laser Irradiation

    Directory of Open Access Journals (Sweden)

    Bing Wang

    2015-08-01

    Full Text Available The effect of laser irradiation on surface wettability of cyclic olefin polymer (COP was investigated. Under different laser parameters, a superhydrophilic or a superhydrophobic COP surface with a water contact angle (WCA of almost 0° or 163°, respectively, could be achieved by direct femtosecond laser irradiation. The laser power deposition rate (PDR was found to be a key factor on the wettability of the laser-treated COP surface. The surface roughness and surface chemistry of the laser-irradiated samples were characterized by surface profilometer and X-ray photoelectron spectroscopy, respectively; they were found to be responsible for the changes of the laser-induced surface wettability. The mechanisms involved in the laser surface wettability modification process were discussed.

  1. Sb Surface Modification of Pd by Mimetic Underpotential Deposition for Formic Acid Oxidation

    OpenAIRE

    Long-Long Wang; Xiao-Lu Cao; Ya-Jun Wang; Qiao-Xia Li

    2015-01-01

    The newly proposed mimetic underpotential deposition (MUPD) technique was extended to modify Pd surfaces with Sb through immersing a Pd film electrode or dispersing Pd/C powder in a Sb(III)-containing solution blended with ascorbic acid (AA). The introduction of AA shifts down the open circuit potential of Pd substrate available to achieve suitable Sb modification. The electrocatalytic activity and long-term stability towards HCOOH electrooxidation of the Sb modified Pd surfaces (film elect...

  2. STUDY ON THE SURFACE MODIFICATION OF NANOMETER CARBON PARTICLES IN ATMOSPHERIC PLASMA

    Institute of Scientific and Technical Information of China (English)

    Y.J. Ge; G.Q. Zhang; Y.M. Liu; X.G. Guo; Z.F. Zhao

    2002-01-01

    The surface modification of nanometer carbon material has been studied by usingan Induced Dielectric Barrier Discharge Plasma device (IDBD). The experimentalresults show that with different work gases and different discharge conditions, thesurface behaviors of carbon black can be changed according to needs, including theuse of different functional groups and the change of the surface roughness of carbonparticles etc., which increased the grinding and dispersion abilities in binder.

  3. Surface Modification Process by Electrical Discharge Machining with Ti Powder Green Compact Electrode

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    This paper describes a new method of surface modification by Electrical Discharge Machining (EDM). By using ordinary EDM machine tool and kerosene fluid, a hard ceramic layer can be created on the workpiece surface with Ti or other compressed powder electrode in a certain condition. This new revolutionary method is called Electrical Discharge Coating (EDC). The process of EDC begins with electrode wear during EDM,then a kind of hard carbide is created through the thermal and chemical reaction between the wo...

  4. Surface hydrophobic modification of cellulose membranes by plasma-assisted deposition of hydrocarbon films

    OpenAIRE

    Mudtorlep Nisoa; Pikul Wanichapichart

    2010-01-01

    Surface modification by plasma polymerization is an efficient method to change the surface properties of a membrane. Desirable functionality such as hydrophobicity or hydrophilicity can be obtained, depending on plasma chemistry of gas precursors and discharge conditions. In this work, RF magnetron plasma is produced using acetylene and nitrogen as precursor gases. Variations of RF power, particle flux, deposited time and pressure of the precursor gases have been made to observe coating effec...

  5. Plasma-Based Surface Modification of Polydimethylsiloxane for PDMS-PDMS Molding

    OpenAIRE

    Lopera, S.; Mansano, R. D.

    2012-01-01

    We present and compare two processes for plasma-based surface modification of Polydimethylsiloxane (PDMS) to achieve the antisticking behavior needed for PDMS-PDMS molding. The studied processes were oxygen plasma activation for vapor phase silanization and plasma polymerization with tetrafluoromethane/hydrogen mixtures under different processing conditions. We analyzed topography changes of the treated surfaces by atomic force microscopy and contact angle measurements. Plasma treatment were ...

  6. Enhancing Plasma Surface Modification using high Intensity and high Power Ultrasonic Acoustic Waves

    DEFF Research Database (Denmark)

    2010-01-01

    This invention relates to a plasma surface modification process (and a corresponding a system) of a solid object (100) comprising creating plasma (104) by a plasma source (106), application of the plasma (104) to at least a part of a surface (314) of the solid object (100), generating ultrasonic...... or a mixture of gases (500) flow in contact with said solid object (100) is thinned or destructed for at least a part of said surface (314). In this way, the plasma can more efficiently access and influence the surface of the solid object to be treated by the plasma, which speeds the process time up...

  7. Surface Modification of Photoresist SU-8 for Low Autofluorescence and Bioanalytical Applications

    DEFF Research Database (Denmark)

    Cao, Cuong; Birtwell, Sam W.; Høgberg, Jonas;

    2011-01-01

    This paper reports a surface modification of epoxy-based negative photoresist SU-8 for reducing its autofluorescence while enhancing its biofunctionality. By covalently depositing a thin layer of 20 nm Au nanoparticles (AuNPs) onto the SU-8 surface, we found that the AuNPs-coated SU-8 surface...... is much less fluorescent than the untreated SU-8. Moreover, DNA probes can easily be immobilized on the Au surface and are thermally stable over a wide range of temperature. These improvements will benefit bioanalytical applications such as DNA hybridization and solid-phase PCR (SP-PCR)....

  8. Synthesis of Perfluorinated Oxetane and Surface Properties of Its Cationic UV Cured Coating as a Reactive Additive

    Institute of Scientific and Technical Information of China (English)

    ZHAN Fu; ZHANG Yong; SHI Wen-fang

    2012-01-01

    Perfluorinated oxetane(F-OXE) was synthesized via the ring-opening reaction of epoxy-functionalized oxetane with 2-(perfluorooctyl)ethanol under base-catalysis,and characterized by FTIR and 1H NMR spectroscopy.The synthesized F-OXE was mixed with a commercial cationic UV curable resin,UVR6110,as a reactive additive at different mass fractions,and UV-irradiation cured in the presence of triphenylsulphonium hexafluoroantimonate as a cationic photoinitiator.The surface property study of cured films indicated that both hydrophobicity and oleophobicity were effectively enhanced by the addition of a small amount of F-OXE.The contact angles of water and 1-bromonaphthalene on the surface of the cured film with 1.0%(mass fraction) F-OXE loading increased from 72° to 106° and from 0° to 76°,respectively,compared with those on the surface of the film without F-OXE addition.The surface tension of UVR6110-F-OXE cured film decreased greatly from 55.6 mN/m of referenced film to 22.9 mN/m.The results from X-ray photoelectron spectroscopy analysis confirm the migration and aggregation effect of perfluoroalkyl group to the surface of cured film.For 1%(mass fraction) addition of F-OXE,the relative content of fluorine greatly increased from 0.70%(mass fraction) in the interior of the cured film to 36.73°%(mass fraction) at the surface of the cured film,whereas those of carbon and oxygen decreased from 73.29% to 40.96% and from 26.00% to22.30%,respectively.

  9. Roughened titanium surfaces with silane and further RGD peptide modification in vitro

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Wen-Cheng, E-mail: wencchen@fcu.edu.tw [Advanced Medical Devices and Composites Laboratory, Department of Fiber and Composite Materials, College of Engineering, Feng Chia University, Taichung 40724, Taiwan, ROC (China); Ko, Chia-Ling [School of Dentistry, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan, ROC (China)

    2013-07-01

    The strategy to achieve osteoregeneration of dental implants during early-stage regeneration is strongly related to surface conditions for achieving highly successful effects after implantation. Surface modifications, namely, mechanical ground, silanization, bonded and sandblasted with pentasequence Gly-Arg-Gly-Asp-Ser (GRGDS) peptide, and acid-etched with Arg-Gly-Asp (RGD) peptide, were compared for their ability to support cell attachment, proliferation, and differentiation on titanium surfaces. The characteristics and comparative in vitro bio-interactions toward osteoprogenitor cells were tested in the four groups with various surface modifications. Compared with the other groups, the sandblasted and acid-etched, and silane with subsequent RGD peptide modified surfaces had the smallest wetting angle, absence of a significant cell viability difference, and largest quantity of alkaline phosphatase production during the expressions of early-stage cell differentiation. The method of synthesizing GRGDS peptides on roughened titanium surfaces has the potential to provide a combination of early bone regeneration and implant of long-term anchored capabilities. Highlights: • The osteoregeneration during early-stage is strongly related to surface conditions. • The wettability with RGD peptide treated surfaces can be enhanced. • Rougher surface binding with RGD peptide can achieve better osseogeneration. • Surfaces with RGD peptide accelerate the progenitor bone cell mineralization.

  10. Effect of Hybrid Surface Modifications on Tensile Properties of Polyacrylonitrile- and Pitch-Based Carbon Fibers

    Science.gov (United States)

    Naito, Kimiyoshi

    2016-05-01

    Recent interest has emerged in techniques that modify the surfaces of carbon fibers, such as carbon nanotube (CNT) grafting or polymer coating. Hybridization of these surface modifications has the potential to generate highly tunable, high-performance materials. In this study, the mechanical properties of surface-modified polyacrylonitrile (PAN)-based and pitch-based carbon fibers were investigated. Single-filament tensile tests were performed for fibers modified by CNT grafting, dipped polyimide coating, high-temperature vapor deposition polymerized polyimide coating, grafting-dipping hybridization, and grafting-vapor deposition hybridization. The Weibull statistical distributions of the tensile strengths of the surface-modified PAN- and pitch-based carbon fibers were examined. All surface modifications, especially hybrid modifications, improved the tensile strengths and Weibull moduli of the carbon fibers. The results exhibited a linear relationship between the Weibull modulus and average tensile strength on a log-log scale for all surface-modified PAN- and pitch-based carbon fibers.

  11. Remarkable fluorescence enhancement versus complex formation of cationic porphyrins on the surface of ZnO nanoparticles

    KAUST Repository

    Aly, Shawkat Mohammede

    2014-06-12

    Fluorescence enhancement of organic fluorophores shows tremendous potential to improve image contrast in fluorescence-based bioimaging. Here, we present an experimental study of the interaction of two cationic porphyrins, meso-tetrakis(1-methylpyridinium-4-yl)porphyrin chloride (TMPyP) and meso-tetrakis(4-N,N,N-trimethylanilinium)porphyrin chloride (TMAP), with cationic surfactant-stabilized zinc oxide nanoparticles (ZnO NPs) based on several steady-state and time-resolved techniques. We show the first experimental measurements demonstrating a clear transition from pronounced fluorescence enhancement to charge transfer (CT) complex formation by simply changing the nature and location of the positive charge of the meso substituent of the cationic porphyrins. For TMPyP, we observe a sixfold increase in the fluorescence intensity of TMPyP upon addition of ZnO NPs. Our experimental results indicate that the electrostatic binding of TMPyP with the surface of ZnO NPs increases the symmetry of the porphyrin macrocycle. This electronic communication hinders the rotational relaxation of the meso unit and/or decreases the intramolecular CT character between the cavity and the meso substituent of the porphyrin, resulting in the enhancement of the intensity of the fluorescence. For TMAP, on the other hand, the different type and nature of the positive charge resulting in the development of the CT band arise from the interaction with the surface of ZnO NPs. This observation is confirmed by the femtosecond transient absorption spectroscopy, which provides clear spectroscopic signatures of photoinduced electron transfer from TMAP to ZnO NPs. © 2014 American Chemical Society.

  12. UV light induced surface modification of HDPE films with bioactive compounds

    Energy Technology Data Exchange (ETDEWEB)

    Daniloska, Vesna; Blazevska-Gilev, Jadranka; Dimova, Vesna [Faculty of Technology and Metallurgy, University St. Cyril and Methodius, Ruger Boskovic 16, 1000 Skopje (Macedonia, The Former Yugoslav Republic of); Fajgar, Radek [Institute of Chemical Process Fundamentals, ASCR, Rozvojova 135, Prague 6-Suchdol (Czech Republic); Tomovska, Radmila, E-mail: radmila_tomovska@ehu.es [Institute for Polymer Materials, POLYMAT, Centro Joxe Mari Korta, University of the Basque Country, P.O. Box 1072, 20080 Donostia-San Sebastian (Spain); IKERBASQUE, Basque Foundation for Science, 48011 Bilbao (Spain)

    2010-01-15

    The development of different techniques for surface modification of polymers becomes popular in a last decade. These techniques preserve useful bulk polymer properties unchanged, while the activation of the polymer surface offers more possibilities for polymer applications. In this work, a new, one-step method for bio-activation of HDPE (high density polyethylene) surface by UV irradiation is presented. HDPE films coupled with selected active compound and a photoinitiator was treated by UV lamp, emitting light at 254 nm. For surface functionalization of HDPE films, the following compounds were employed: 2-aminopyridine (AP), N{sup 1}-(2-pyridylaminomethyl)-1,2,4-triazole (TA) and benzocaine (BC). The influence of irradiation time on the extent of surface changes was investigated. The modified polymer surfaces were investigated by Fourier transformed infrared (FTIR) and Raman spectroscopy, scanning electron microscopy (SEM) and contact angle measurements, demonstrating successful functionalization of HDPE surface.

  13. LDPE Surface Modifications Induced by Atmospheric Plasma Torches with Linear and Showerhead Configurations

    CERN Document Server

    Rich, Sami Abou; Leroy, Perrine; Reniers, François; Nittler, Laurent; Pireaux, Jean-Jacques

    2016-01-01

    Low density polyethylene (LDPE) surfaces have been plasma modified to improve their nanostructural and wettability properties. These modifications can significantly improve the deposition of subsequent layers such as films with specific barrier properties. For this purpose, we compare the treatments induced by two atmospheric plasma torches with different configurations (showerhead vs. linear). The modifications of LDPE films in terms of chemical surface composition and surface morphology are evidenced by X-ray photoelectron spectro-scopy, water contact angles measurements, and atomic force microscopy. A comparison between the two post-discharge treatments is achieved for several torch-to-substrate distances (gaps), treatment times, and oxygen flow rates in terms of etching rate, roughening rate, diffusion of oxygen into the subsur-face and hydrophilicity. By correlating these results with the chemical composition of the post-discharges, we identify and compare the 'species which are responsible for the chemi...

  14. Sb Surface Modification of Pd by Mimetic Underpotential Deposition for Formic Acid Oxidation

    Directory of Open Access Journals (Sweden)

    Long-Long Wang

    2015-07-01

    Full Text Available The newly proposed mimetic underpotential deposition (MUPD technique was extended to modify Pd surfaces with Sb through immersing a Pd film electrode or dispersing Pd/C powder in a Sb(III-containing solution blended with ascorbic acid (AA. The introduction of AA shifts down the open circuit potential of Pd substrate available to achieve suitable Sb modification. The electrocatalytic activity and long-term stability towards HCOOH electrooxidation of the Sb modified Pd surfaces (film electrode or powder catalyst by MUPD is superior than that of unmodified Pd and Sb modified Pd surfaces by conventional UPD method. The enhancement of electrocatalytic performance is due to the third body effect and electronic effect, as well as bi-functional mechanism induced by Sb modification which result in increased resistance against CO poisoning.

  15. Surface modification of ferritic steels using MEVVA and duoplasmatron ion sources.

    Science.gov (United States)

    Kulevoy, Timur V; Chalyhk, Boris B; Fedin, Petr A; Sitnikov, Alexey L; Kozlov, Alexander V; Kuibeda, Rostislav P; Andrianov, Stanislav L; Orlov, Nikolay N; Kravchuk, Konstantin S; Rogozhkin, Sergey V; Useinov, Alexey S; Oks, Efim M; Bogachev, Alexey A; Nikitin, Alexander A; Iskandarov, Nasib A; Golubev, Alexander A

    2016-02-01

    Metal Vapor Vacuum Arc (MEVVA) ion source (IS) is a unique tool for production of high intensity metal ion beam that can be used for material surface modification. From the other hand, the duoplasmatron ion source provides the high intensity gas ion beams. The MEVVA and duoplasmatron IS developed in Institute for Theoretical and Experimental Physics were used for the reactor steel surface modification experiments. Response of ferritic-martensitic steel specimens on titanium and nitrogen ions implantation and consequent vacuum annealing was investigated. Increase in microhardness of near surface region of irradiated specimens was observed. Local chemical analysis shows atom mixing and redistribution in the implanted layer followed with formation of ultrafine precipitates after annealing.

  16. Surface modification of ferritic steels using MEVVA and duoplasmatron ion sources

    Energy Technology Data Exchange (ETDEWEB)

    Kulevoy, Timur V., E-mail: kulevoy@itep.ru; Orlov, Nikolay N.; Rogozhkin, Sergey V.; Bogachev, Alexey A.; Nikitin, Alexander A.; Iskandarov, Nasib A.; Golubev, Alexander A. [State Scientific Center of the Russian Federation, Institute for Theoretical and Experimental Physics of National Research Centre “Kurchatov Institute,” Moscow (Russian Federation); National Research Nuclear University MEPhI (Moscow Engineering Physics Institute), Moscow (Russian Federation); Chalyhk, Boris B.; Fedin, Petr A.; Sitnikov, Alexey L.; Kozlov, Alexander V.; Kuibeda, Rostislav P.; Andrianov, Stanislav L. [State Scientific Center of the Russian Federation, Institute for Theoretical and Experimental Physics of National Research Centre “Kurchatov Institute,” Moscow (Russian Federation); Kravchuk, Konstantin S.; Useinov, Alexey S. [Technological Institute for Superhard and Novel Carbon Materials, Moscow (Russian Federation); Oks, Efim M. [Institute of High Current Electronics SB RAS, Tomsk (Russian Federation); Tomsk State University of Control System and Radioelectronics, Tomsk (Russian Federation)

    2016-02-15

    Metal Vapor Vacuum Arc (MEVVA) ion source (IS) is a unique tool for production of high intensity metal ion beam that can be used for material surface modification. From the other hand, the duoplasmatron ion source provides the high intensity gas ion beams. The MEVVA and duoplasmatron IS developed in Institute for Theoretical and Experimental Physics were used for the reactor steel surface modification experiments. Response of ferritic-martensitic steel specimens on titanium and nitrogen ions implantation and consequent vacuum annealing was investigated. Increase in microhardness of near surface region of irradiated specimens was observed. Local chemical analysis shows atom mixing and redistribution in the implanted layer followed with formation of ultrafine precipitates after annealing.

  17. Surface modification of oxide layer on Si using highly charged ions

    Energy Technology Data Exchange (ETDEWEB)

    Sakurai, M., E-mail: msakurai@kobe-u.ac.jp [Department of Physics, Kobe University, Rokkodai, Nada-ku, Kobe 657-8501 (Japan); Liu, S.; Sakai, S. [Department of Physics, Kobe University, Rokkodai, Nada-ku, Kobe 657-8501 (Japan); Ohtani, S. [Institute for Laser Science, University of Electro-Communications, Chofu, Tokyo 182-8585 (Japan); Terui, T. [National Institute of Information and Communications Technology, Iwaoka, Nishi-ku, Kobe 651-2492 (Japan); Sakaue, H.A. [National Institute for Fusion Science, Oroshi-cho, Toki 509-5292 (Japan)

    2013-11-15

    Surface modification using highly charged ions is presented. The surface of a Si wafer which is covered with a native oxide layer is used as a sample. The sample was irradiated with Ar{sup 11+} ions at a fluence of 10{sup 13}–10{sup 14}/cm{sup 2}. The Ar{sup 11+} ions were obtained from an electron beam ion source (Kobe EBIS). The surface was investigated using secondary electron microscopy, X-ray photoelectron spectroscopy and high-resolution electron energy loss spectroscopy. The obtained results suggest that the native oxide layer is sputtered by the irradiation of Ar{sup 11+} ions and that the structural modification makes the density of the oxide layer lower and the electric conductivity higher.

  18. Towards Enhanced Performance Thin-film Composite Membranes via Surface Plasma Modification

    Science.gov (United States)

    Reis, Rackel; Dumée, Ludovic F.; Tardy, Blaise L.; Dagastine, Raymond; Orbell, John D.; Schutz, Jürg A.; Duke, Mikel C.

    2016-07-01

    Advancing the design of thin-film composite membrane surfaces is one of the most promising pathways to deal with treating varying water qualities and increase their long-term stability and permeability. Although plasma technologies have been explored for surface modification of bulk micro and ultrafiltration membrane materials, the modification of thin film composite membranes is yet to be systematically investigated. Here, the performance of commercial thin-film composite desalination membranes has been significantly enhanced by rapid and facile, low pressure, argon plasma activation. Pressure driven water desalination tests showed that at low power density, flux was improved by 22% without compromising salt rejection. Various plasma durations and excitation powers have been systematically evaluated to assess the impact of plasma glow reactions on the physico-chemical properties of these materials associated with permeability. With increasing power density, plasma treatment enhanced the hydrophilicity of the surfaces, where water contact angles decreasing by 70% were strongly correlated with increased negative charge and smooth uniform surface morphology. These results highlight a versatile chemical modification technique for post-treatment of commercial membrane products that provides uniform morphology and chemically altered surface properties.

  19. Synthesis and Characteristics of Mesoporous Silica Aerogels with One-step Solvent Exchange/Surface Modification

    Institute of Scientific and Technical Information of China (English)

    WANG Lijiu; ZHAO Shanyu

    2009-01-01

    The synthesis procedures and physical properties of the ambient dried hydrophobic silica aerogels by using different contents of ethanol(EtOH)/trimethylchlorosilane(TMCS)/n-Hexane as surface modification agent were investigated.One-step solvent exchange and surface modification were simultaneously progressed by immersing silica hydrogels in EtOH/TMCS/n-Hexane solution.It is found that microstructures as well as properties of silica aerogels like porosity,specific density and specific surface area are affected by the contents of surface modification agent in the sol from the re-sults of SEM,TEM morphology,FT-IR chemical structure,BET surface area and BJH pore size analyses.The volume of TMCS is of 10%and 20%of hydrogels,and the final product is hydrophilic xerogels.When TMCS's percent(v/v)is elevated to 75%-100%,hydrophobic silica aerogels with good performance are synthesized,the porosities of aerogels are in the range of 93.5%-95.8%and the av-erage pore size diameter is less than 20 nm.

  20. Surface monofunctionalized polymethyl pentene hollow fiber membranes by plasma treatment and hemocompatibility modification for membrane oxygenators

    Science.gov (United States)

    Huang, Xin; Wang, Weiping; Zheng, Zhi; Fan, Wenling; Mao, Chun; Shi, Jialiang; Li, Lei

    2016-01-01

    The hemocompatibility of polymethyl pentene (PMP) hollow fiber membranes (HFMs) was improved through surface modification for membrane oxygenator applications. The modification was performed stepwise with the following: (1) oxygen plasma treatment, (2) functionalization of monosort hydroxyl groups through NaBH4 reduction, and (3) grafting 2-methacryloyloxyethyl phosphorylcholine (MPC) or heparin. SEM, ATR-FTIR, and XPS analyses were conducted to confirm successful grafting during the modification. The hemocompatibility of PMP HFMs was analyzed and compared through protein adsorption, platelet adhesion, and coagulation tests. Pure CO2 and O2 permeation rates, as well as in vitro gas exchange rates, were determined to evaluate the mass transfer properties of PMP HFMs. SEM results showed that different nanofibril topographies were introduced on the HFM surface. ATR-FTIR and XPS spectra indicated the presence of functionalization of monosort hydroxyl group and the grafting of MPC and heparin. Hemocompatibility evaluation results showed that the modified PMP HFMs presented optimal hemocompatibility compared with pristine HFMs. Gas permeation results revealed that gas permeation flux increased in the modified HFMs because of dense surface etching during the plasma treatment. The results of in vitro gas exchange rates showed that all modified PMP HFMs presented decreased gas exchange rates because of potential surface fluid wetting. The proposed strategy exhibits a potential for fabricating membrane oxygenators for biomedical applications to prevent coagulation formation and alter plasma-induced surface topology and composition.

  1. Enhancing the formation and shear resistance of nitrifying biofilms on membranes by surface modification.

    Science.gov (United States)

    Lackner, Susanne; Holmberg, Maria; Terada, Akihiko; Kingshott, Peter; Smets, Barth F

    2009-08-01

    Polypropylene (PP) membranes and polyethylene (PE) surfaces were modified to enhance formation and shear resistance of nitrifying biofilms for wastewater treatment applications. A combination of plasma polymerization and wet chemistry was employed to ultimately introduce poly(ethyleneglycol) (PEG) chains with two different functional groups (-PEG-NH(2) and -PEG-CH(3)). Biofilm growth experiments using a mixed nitrifying bacterial culture revealed that the specific combination of PEG chains with amino groups resulted in most biofilm formation on both PP and PE samples. Detachment experiments showed similar trends: biofilms on -PEG-NH(2) modified surfaces were much stronger compared to the other modifications and the unmodified reference surfaces. Electrostatic interactions between the protonated amino group and negatively charged bacteria as well as PEG chain density which can affect the surface structure might be possible explanations of the superiority of the -PEG-NH(2) modification. The success of the-PEG-NH(2) modification was independent of the original surface and might, therefore, be used in wastewater treatment bioreactors to improve reactor performance by making biofilm formation more stable and predictable.

  2. Cell adhesive and antifouling polyvinyl chloride surfaces via wet chemical modification.

    Science.gov (United States)

    Gabriel, Matthias; Strand, Dennis; Vahl, Christian-Friedrich

    2012-09-01

    Polyvinyl chloride (PVC) is one of the most frequently used polymers for the manufacturing of medical devices. Limitations for its usage are based upon unfavorable surface properties of the polymer including its hydrophobicity and lack of functionalities in order to increase its versatility. To address this issue, wet chemical modification of PVC was performed through surface amination using the bifunctional compound ethylene diamine. The reaction was conducted in order to achieve maximum surface amination while leaving the bulk material unaffected. The initial activation step was characterized by means of various methods including contact angle measurements, colorimetric amine quantification, infrared spectroscopy, and gel permeation chromatography. Depth profiles were obtained by a confocal microscopic method using fluorescence labeling. Exclusive surface modification was thus confirmed. To demonstrate biological applications of the presented technique, two examples were chosen: The covalent immobilization of the cell adhesive Asp-Gly-Asp-Ser-peptide (RGD) onto PVC samples yielded a surface that strongly supported cellular adhesion and proliferation of fibroblasts. In contrast, the decoration of PVC with the hydrophilic polymer polyethylene glycol prevented cellular adhesion to a large extent. The impact of these modifications was demonstrated by cell culture experiments.

  3. Acid/base bifunctional carbonaceous nanomaterial with large surface area: Preparation, characterization, and adsorption properties for cationic and anionic compounds

    Energy Technology Data Exchange (ETDEWEB)

    Li, Kai; Ma, Chun–Fang; Ling, Yuan; Li, Meng [Department of Chemistry, Faculty of Material Science and Chemistry, China University of Geosciences, Wuhan 430074 (China); Gao, Qiang, E-mail: gaoqiang@cug.edu.cn [Department of Chemistry, Faculty of Material Science and Chemistry, China University of Geosciences, Wuhan 430074 (China); Engineering Research Center of Nano-Geo Materials of Ministry of Education, China University of Geosciences, Wuhan 430074 (China); Luo, Wen–Jun, E-mail: heartnohome@yahoo.com.cn [Department of Chemistry, Faculty of Material Science and Chemistry, China University of Geosciences, Wuhan 430074 (China)

    2015-07-15

    Nanostructured carbonaceous materials are extremely important in the nano field, yet developing simple, mild, and “green” methods that can make such materials possess large surface area and rich functional groups on their surfaces still remains a considerable challenge. Herein, a one-pot and environment-friendly method, i.e., thermal treatment (180 °C; 18 h) of water mixed with glucose and chitosan (CTS), has been proposed. The resultant carbonaceous nanomaterials were characterized by field emitting scanning electron microscope, N{sub 2} adsorption/desorption, Fourier transform infrared spectroscope, X-ray photoelectron spectroscopy, and zeta-potential analysis. It was found that, in contrast to the conventional hydrothermally carbonized product from pure glucose, with low surface area (9.3 m{sup 2} g{sup −1}) and pore volume (0.016 cm{sup 3} g{sup −1}), the CTS-added carbonaceous products showed satisfactory textural parameters (surface area and pore volume up to 254 m{sup 2} g{sup −1} and 0.701 cm{sup 3} g{sup −1}, respectively). Moreover, it was also interestingly found that these CTS-added carbonaceous products possessed both acidic (–COOH) and basic (–NH{sub 2}) groups on their surfaces. Taking the advantages of large surface area and –COOH/–NH{sub 2} bifunctional surface, the carbonaceous nanomaterials exhibited excellent performance for adsorptions of cationic compound (i.e., methylene blue) at pH 10 and anionic compound (i.e., acid red 18) at pH 2, respectively. This work not only provides a simple and green route to prepare acid/base bifunctional carbonaceous nanomaterials with large surface area but also well demonstrates their potential for application in adsorption. - Highlights: • A simple and green method was proposed to prepare carbon nanomaterials. • The carbon product showed acid/base bifunctional surface with large surface area. • The carbon material could efficiently adsorb both cationic and anionic compounds.

  4. Tailoring activated carbon by surface chemical modification with O, S, and N containing molecules

    Directory of Open Access Journals (Sweden)

    Rachel RibeiroVieira Azzi Rios

    2003-06-01

    Full Text Available In this work the surface of activated carbon was chemically modified in order to introduce O, S and N containing groups. The activated carbon surface was selectively oxidized with concentrated HNO3 under controlled conditions. Characterization by thermogravimetric analyses, infrared spectroscopy and NaOH titration suggested the formation of mainly -COOH and small amounts of -OH groups, with concentration of approximately 4.10(21 groups/g of carbon. These -COOH functionalized carbons showed high adsorption capacity for metal cations in aqueous solution in the following order: Pb+2>Cu+2>Ni+2 >Cd+2~Co+2>Ca+2 , suggesting a cation exchange mechanism via a surface complex [COO-M+2]. These -COOHsurf groups can be reacted with SOCl2 to produce a surface acylchloride group, -COCl. This surface -COCl group proved to be a very reactive and versatile intermediate for the grafting of different S and N containing molecules onto the carbon surface, such as 1,2-ethaneditiol (EDT-, HSCH2CH2SH 1,7-dimercapto-4-thioheptane (DMTH-HSCH2CH2CH2SCH2CH 2CH2SH or 1,2-ethylenediamine (EDA- NH2CH2CH2NH2 and triethyltetraamine, TEA (H2NCH2CH2NHCH2CH 2NHCH2CH2 NH2. The characterization of these materials was carried out by TG, IR and TPDMS (Temperature Programmed Decomposition Mass Spectrometry experiments suggesting the formation of thioesther and amide surface groups, i.e. -COSR and -CONHR, with yields of approximately 50 and 75% for the reaction with DME and EDA, respectively. Preliminary adsorption experiments showed that these materials can efficiently remove metals such as Pb+2, Cu+2 and Ni+2 from aqueous medium.

  5. Surface modification of InGaAs/GaAs heterostructures by swift heavy ion irradiation

    Science.gov (United States)

    Dhamodaran, S.; Pathak, A. P.; Avasthi, D. K.; Srinivasan, T.; Muralidharan, R.; Emfietzoglou, D.

    2007-04-01

    We investigate the surface morphology of molecular beam epitaxy (MBE) grown InGaAs/GaAs(0 0 1) heterostructures using atomic force microscope (AFM) before and after irradiation. Samples with layer thicknesses below critical layer thickness (i.e. fully strained) have smooth surface where as, the samples grown beyond critical layer thickness have cross hatch patterns at the surface. The transition from smooth to cross-hatch pattern may be used to identify the onset of strain relaxation. The samples were subjected to swift heavy ion (SHI) irradiation using 150 MeV Ag12+ ions with a fixed fluence of 1 × 1013 ions/cm2. The morphology of the strained samples was almost similar before and after irradiation where as, the partially relaxed samples were observed to have variations. The electronic energy loss of the incident ions which is dominant compared to the nuclear energy loss is effective to modify with the fluence used in the present study for partially relaxed samples. The relaxation of excited electron subsystem of the target results in the melting and re-growth which reflects in the surface morphology. The observed modifications at the surface may be attributed to (i) irradiation induced surface mass transport and (ii) interface modifications, where both these factors determine the surface morphology of heterostructures. The effects of irradiation on the surface and interface of the samples have been realized by AFM studies.

  6. Effect of surface modification on carbon fiber and its reinforced phenolic matrix composite

    Science.gov (United States)

    Yuan, Hua; Wang, Chengguo; Zhang, Shan; Lin, Xue

    2012-10-01

    In this work, polyacrylonitrile (PAN)-based carbon fiber were chemically modified with H2SO4, KClO3 and silane coupling agent (γ-aminopropyltriethoxysilane, APS), and carbon fiber reinforced phenolic matrix composites were prepared. The structural and surface characteristics of the carbon fiber were investigated by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), laser Raman scattering (LRS) and Fourier transform infrared spectroscopy (FTIR). Single fiber mechanical properties, specific surface area, composite impact properties and interfacial shear strength (ILSS) were researched to indicate the effects of surface modification on fibers and the interaction between modified fiber surface and phenolic matrix. The results showed that carbon fiber surface modification by oxidation and APS can strengthen fiber surface chemical activity and enlarge the fiber surface area as well as its roughness. When carbon fiber (CF) is oxidized treatment, the oxygen content as well as the O/C ratio will be obviously increased. Oxygen functional groups increase with oxidation time increasing. Carbon fiber treated with APS will make Csbnd Osbnd R content increase and Osbnd Cdbnd O content decrease due to surface reaction. Proper treatment of carbon fiber with acid and silane coupling agent prove an effective way to increase the interfacial adhesion and improve the mechanical and outdoor performance of the resulting fiber/resin composites.

  7. Effects of surface modification on electrochemical performance of MnO2

    Institute of Scientific and Technical Information of China (English)

    LIU Li-qing; WANG Jjan-ming; FAN Yu-kai; WANG Guo-guang; ZHANG Jian-qing

    2005-01-01

    The MnO2 samples coated with Ca(OH)2 were prepared by a liquid-phase surface treatment method.The physical properties of the samples were examined by SEM, EDAX and chemical analysis, and their electrochemical performances were investigated by means of galvanostatic charge-discharge, cyclic voltammetry and electrochemical impedance spectroscopy (EIS). The SEM results show that the samples coated with Ca(OH)2 display a porous surface structure. The electrochemical experiments indicate that the surface modification decreases the polarization of MnO2 electrodes and improves their discharge potentials and discharge capacities.

  8. Nanocapillary Atmospheric Pressure Plasma Jet: A Tool for Ultrafine Maskless Surface Modification at Atmospheric Pressure.

    Science.gov (United States)

    Motrescu, Iuliana; Nagatsu, Masaaki

    2016-05-18

    With respect to microsized surface functionalization techniques we proposed the use of a maskless, versatile, simple tool, represented by a nano- or microcapillary atmospheric pressure plasma jet for producing microsized controlled etching, chemical vapor deposition, and chemical modification patterns on polymeric surfaces. In this work we show the possibility of size-controlled surface amination, and we discuss it as a function of different processing parameters. Moreover, we prove the successful connection of labeled sugar chains on the functionalized microscale patterns, indicating the possibility to use ultrafine capillary atmospheric pressure plasma jets as versatile tools for biosensing, tissue engineering, and related biomedical applications.

  9. Surface modification of polyester film by glow discharge tunnel at atmospheric pressure

    Institute of Scientific and Technical Information of China (English)

    XU Xiang-yu; WANG Shou-guo; YE Tian-chun; JING Guang-yin; YU Da-peng

    2004-01-01

    A large-area improved dielectric barrier glow discharge tunnel has been developed for modifying the surface of polyester film at atmospheric pressure with argon and oxygen gas mixtures. The electrical properties of the glow discharge tunnel were studied by simultaneous measurement of the voltage and current. In addition, the effect of the glow discharge tunnel treatment on the surface of polyester film were studied. The resultant modifications of the surface properties of the treated samples were investigated through scanning probe microscopy and contact angle measurement.

  10. Effects of Surface-modification of Carbon Black on the Characteristics of Polymerized Toner

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Eun Ho; Kim, Dae Su [Chungbuk National University, Cheongju (Korea, Republic of)

    2013-10-15

    Carbon black was surface-modified to prepare styrene-based suspension polymerized toner with excellent carbon black dispersibility inside toner particles. Carbon black was oxidized first to introduce hydroxyl groups on the surfaces, then esterification between the hydroxyl groups and carboxyl groups of organic acids (oleic acid, palmitic acid, acrylic acid) was followed to obtain organically surface-modified carbon black. The surface-modification of carbon black was confirmed by FTIR. Apparent carbon black dispersibility in the monomer mixture of the binder resin was tested and the particle size of dispersed carbon black was measured by particle size analyzer. Optical micrographs showed that carbon black dispersibility inside toner particles was improved considerably when the carbon black surface-modified with oleic acid was used. The polymerized toner prepared with the carbon black surface-modified with oleic acid showed ideal particle size and size distribution as a toner.

  11. Coadsorption of low-molecular weight aromatic and aliphatic alcohols and acids with the cationic surfactant, CTAB, on silica surfaces.

    Science.gov (United States)

    Wangchareansak, Thipvaree; Keniry, Max A; Liu, Guangming; Craig, Vincent S J

    2014-06-17

    We have investigated the coadsorption of a range of small molecules with the cationic surfactant CTAB to silica surfaces over a range of concentrations and CTAB to solute ratios and compared the coadsorption with adsorption in the presence of the salicylate ion. We find that molecules with aromatic character and molecules with double bonds are most favorably adsorbed, and we attribute this to cation-π bonding between the surfactant headgroups and the π orbitals of the unsaturated bonds of the solute molecules. The adsorption is complex and depends on chemical interactions between the solute molecules and the surfactant, which are highly specific to the structure of the solute. To improve our understanding of the specifics of these interactions, we have performed one-dimensional rotating frame Overhauser spectroscopy (ROESY) nuclear magnetic resonance experiments. These experiments show the complexity of the intermolecular interactions and can be used to determine the position of the solute molecule with regard to the CTAB molecules in the adsorbed aggregates. The ROESY spectrum for the salicylate anion is distinct from those of the other solute molecules and suggests that the anions are dimerizing. Along with the cation-π bonding between the dimers, this provides a model for the strong influence that salicylate has on adsorption, micellar structure, and viscoelasticity. The ROESY data indicate that the catechol molecule interacts with all parts of the surfactant alkane chains such that they wrap around the molecule, but this has little effect on the interfacial curvature or aggregate shape. More intense isophthalic acid-CTAB intermolecular ROEs compared to those of other aromatic solutes are consistent with an interaction between isophthalic acid and the headgroups of two surfactant molecules that slows the intramicellar motion of isophthalic acid. Differences in interactions between solute molecules and the aliphatic surfactant chains do not result in changes

  12. XPS STUDIES ON SURFACE MODIFIED POLY[1-(TRIMETHYLSILYL)-1-PROPYNE] MEMBRANES Ⅱ SURFACE MODIFICATION BY BROMINE VAPOR

    Institute of Scientific and Technical Information of China (English)

    XU Guanfan; SUN Xiaoguang; QIU Xuepeng; ZHANG Jinlan; ZHENG Guodong

    1994-01-01

    Surface modification of poly [ 1-(trimethylsilyl )-1-propyne ] ( PTMSP ) membranes by bromine vapor has been studied. It is shown that Br/C atomic ratio at the surfacesincreased with the time of bromination until about 60 min, then it reached a plateau. The results of XPS and IR studies indicated that the addition of bromine to double bonds and the replacement of H on CH3 by bromine had taken place so that a new peak at 286.0 eV (C-Br)in C1sspectra and some new bands, e. g. at 1220 and 580cm-1,in IR spectra were formed. The fact, Po2, permeability of oxygen, decreased and αO2/N2, separation factor of oxygen relative to nitrogen, increased with bromination time, shows that surface modification of PTMSP by bromine may be an efficient approachto prepare PTMSP membranes used for practical gas separations.

  13. Surface modification of a POSS-nanocomposite material to enhance cellular integration of a synthetic bioscaffold.

    Science.gov (United States)

    Crowley, Claire; Klanrit, Poramate; Butler, Colin R; Varanou, Aikaterini; Platé, Manuela; Hynds, Robert E; Chambers, Rachel C; Seifalian, Alexander M; Birchall, Martin A; Janes, Sam M

    2016-03-01

    Polyhedral oligomeric silsesquioxane poly(carbonate-urea) urethane (POSS-PCU) is a versatile nanocomposite biomaterial with growing applications as a bioscaffold for tissue engineering. Integration of synthetic implants with host tissue can be problematic but could be improved by topographical modifications. We describe optimization of POSS-PCU by dispersion of porogens (sodium bicarbonate (NaHCO3), sodium chloride (NaCl) and sucrose) onto the material surface, with the principle aim of increasing surface porosity, thus providing additional opportunities for improved cellular and vascular ingrowth. We assess the effect of the porogens on the material's mechanical strength, surface chemistry, wettability and cytocompatibilty. Surface porosity was characterized by scanning electron microscopy (SEM). There was no alteration in surface chemistry and wettability and only modest changes in mechanical properties were detected. The size of porogens correlated well with the porosity of the construct produced and larger porogens improved interconnectivity of spaces within constructs. Using primary human bronchial epithelial cells (HBECs) we demonstrate moderate in vitro cytocompatibility for all surface modifications; however, larger pores resulted in cellular aggregation. These cells were able to differentiate on POSS-PCU scaffolds. Implantation of the scaffold in vivo demonstrated that larger pore sizes favor cellular integration and vascular ingrowth. These experiments demonstrate that surface modification with large porogens can improve POSS-PCU nanocomposite scaffold integration and suggest the need to strike a balance between the non-porous surfaces required for epithelial coverage and the porous structure required for integration and vascularization of synthetic scaffolds in future construct design.

  14. Studies on visual detection and surface modification testing of glass microfiber filter paper based biosensor.

    Science.gov (United States)

    Adiguzel, Yekbun; Kulah, Haluk

    2014-04-15

    Glass microfibers are commonly used as biomolecule adsorption media, as structural or disposable components of the optical biosensors. While any improvement in these components are appreciated, utilizing basic tools of traditional approaches may lead to original sensor opportunities as simple, functional designs that can be easily disseminated. Following this pursuit, surface modification of glass microfiber paper surface was performed by 3-aminopropyltriethoxysilane (APTES) and resulting improvement in the cell entrapment capacity could be observed visually, only after Gram staining. Gram staining offered rapid validation of enhanced binding on the glass surface. The same APTES-modified samples were also tested for binding of complementary DNA sequences and the results were less straightforward due to the necessity of DNA visualization by using a fluorescent stain, YOYO-1. Accordingly, when there were no surface modification, DNA and YOYO-1 adsorbed readily on the glass microfiber filter paper, and prolonged the interaction between DNA and YOYO-1. YOYO-1 adsorption on glass could be recognized from the color profile of YOYO-1 emission. This phenomenon can be used to examine suitability of APTES coverage on glass surfaces since YOYO-1 emission can be distinguished by its glass adsorbed versus DNA-bound forms. Aptness of surface coverage is vital to biosensor studies in the sense that it is preceding the forthcoming surface modifications and its precision is imperative for attaining the anticipated interaction kinetics of the surface-immobilized species. The proposed testing scheme offered in this study secures the work, which is aimed to be carried out utilizing such sensing systems and device components.

  15. Enhanced power efficiency of ZnO based organic/inorganic solar cells by surface modification

    Science.gov (United States)

    Tang, Shuangshuang; Tang, Ning; Meng, Xiuqing; Huang, Shihua; Hao, Yafei

    2016-09-01

    We present series of strategies to enhance efficiency of ZnO nanorods based organic/inorganic solar cells with spin-coated P3HT:PCBM blend as active layer. The performance of the as-fabricated devices is improved by controlling the size of ZnO nanorods, annealing temperature and time of active layer, surface modification of ZnO with PSBTBT. Optimized device of ITO/ZnO nanorod/P3HT:PCBM/Ag device with PSBTBT surface modification and air exposure reaches an efficiency of 2.02% with a short-circuit current density, open-circuit voltage and fill factor of 13.23 mA cm-2, 0.547 V and 28%, respectively, under AM 1.5 irradiation of 100 mW m-2, the increase in efficiency is 7-fold of the PSBTBT surface modified ITO/ZnO nanorods/P3HT:PCBM/Ag device compared with the unmodified one, which is own to the increased interface contact, expanded light absorption, tailored band alignment attributed to PSBTBT. We found exposure to air and surface modification is crucial to improve the device performance, and we discussed the mechanisms that affect the performance of the devices in detail.

  16. FE-SEM COMPARATIVE STUDY ON SURFACE MODIFICATION OF WOOL FIBER AFTER DIFFERENT CHEMICAL TREATMENTS

    Directory of Open Access Journals (Sweden)

    BONET-ARACIL Marilés

    2016-05-01

    Full Text Available Wool surface comprehends numerous scales which are responsible of certain undesirable behavior of this fiber during its use and maintenance. One of the most significant issues is related to shrinkage, caused during washing, as a consequence of friction between the fibers. Chemical modification of wool is considered a useful option to avoid these kind of circumstances. During the last years, multiple alternatives for chemical modification of wool have been studied, comprising enzymes or acids amongst others. In this case of study, three different treatments were carried out in order to evaluate wool morphological appearance. The first treatment was an oxidative procedure, containing Basolan DC and sodium acetate as the main components. The second treatment was accomplished using Lanaperm VPO, a commercial finishing agent for wool fiber that claims to soften its surface. The third finishing process was performed employing Siligen FA, a commercial agent intended to act as an antimigrant for dye baths and also provide a smoother and regular surface. After said treatments, microphotographs of all treated and untreated fibers were taken so that a comparison between final appearance could be done. Analyzing results and conclusions, it can be stated that chemical modification of fiber does change its surface appearance and, consequently, its behaviour. Oxidation, Lanaperm, Siligen, wool cuticle, scales

  17. Rapid synthesis of water-glass based aerogels by in situ surface modification of the hydrogels

    Science.gov (United States)

    Bhagat, Sharad D.; Kim, Yong-Ha; Ahn, Young-Soo; Yeo, Jeong-Gu

    2007-01-01

    The objective of the present research was to reduce the processing time of water-glass based aerogels synthesized via an ambient pressure drying. For this purpose we employed a co-precursor method for the surface modification in hydrogels using trimethylchlorosilane (TMCS) and hexamethyldisilazane (HMDS). The surface modification resulted in the displacement of pore water from the hydrogels and thereby absolutely avoiding the time-consuming solvent exchange step. The attachment of trymethylsilyl ( sbnd Si(CH 3) 3) groups to the silica surface was confirmed by the presence of Si sbnd CH 3 peaks at 2900, 1400, 1255 and 845 cm -1 in the Fourier Transform Infrared (FTIR) spectra. The differential thermal analysis (DTA) revealed that the aerogels maintain their hydrophobic behavior up to a maximum temperature of 500 °C above which they become hydrophilic. The physical and textural properties of the silica aerogels have been reported and the results have been discussed by taking into account the surface modification and the amounts of the pore water displaced out from the hydrogels.

  18. Electrochemical behavior of SUS316L stainless steel after surface modification

    Institute of Scientific and Technical Information of China (English)

    梁成浩; 郭亮; 陈婉; 刘敬肖

    2003-01-01

    The surface modification for SUS316L stainless steel was carried out by electroplating Rh, ion beam assisted deposition Ta2O5 and sol-gel-derived TiO2. In Tyrodes stimulated body fluid, the surface modified samples were investigated with electrochemical techniques. The results indicate that the electrochemical stability and dissolution are improved significantly after surface modification. Moreover, as to ion beam assisted deposition Ta2O5 and sol-gel-derived TiO2 film, the metals d orbit electron holes filled up by the oxygen electrons make against the adsorption of hydrogen. Thus the cathode process, which is controlled by the hydrogen reduction, is held back. X-ray diffraction analysis of SUS316L stainless steel after surface modification reveal that each method forms the uniform and compact film on SUS316L stainless steel. These films prevent the dissolving of elements and improve passivation property of the SUS316L stainless steel.

  19. Surface modification of battery electrodes via electroless deposition with improved performance for Na-ion batteries.

    Science.gov (United States)

    Lahiri, Abhishek; Olschewski, Mark; Gustus, René; Borisenko, Natalia; Endres, Frank

    2016-06-01

    Sodium-ion batteries (SIBs) are emerging as potential stationary energy storage devices due to the abundance and low cost of sodium. A simple and energy efficient strategy to develop electrodes for SIBs with a high charge/discharge rate is highly desirable. Here we demonstrate that by surface modification of Ge, using electroless deposition in SbCl3/ionic liquids, the stability and performance of the anode can be improved. This is due to the formation of GexSb1-x at the surface leading to better diffusion of Na, and the formation of a stable twin organic and inorganic SEI which protects the electrode. By judicious control of the surface modification, an improvement in the capacity to between 50% and 300% has been achieved at high current densities (0.83-8.4 A g(-1)) in an ionic liquid electrolyte NaFSI-[Py1,4]FSI. The results clearly demonstrate that an electroless deposition based surface modification strategy in ionic liquids offers exciting opportunities in developing superior energy storage devices.

  20. Nonthermal plasma technology as a versatile strategy for polymeric biomaterials surface modification: a review.

    Science.gov (United States)

    Desmet, Tim; Morent, Rino; De Geyter, Nathalie; Leys, Christophe; Schacht, Etienne; Dubruel, Peter

    2009-09-14

    In modern technology, there is a constant need to solve very complex problems and to fine-tune existing solutions. This is definitely the case in modern medicine with emerging fields such as regenerative medicine and tissue engineering. The problems, which are studied in these fields, set very high demands on the applied materials. In most cases, it is impossible to find a single material that meets all demands such as biocompatibility, mechanical strength, biodegradability (if required), and promotion of cell-adhesion, proliferation, and differentiation. A common strategy to circumvent this problem is the application of composite materials, which combine the properties of the different constituents. Another possible strategy is to selectively modify the surface of a material using different modification techniques. In the past decade, the use of nonthermal plasmas for selective surface modification has been a rapidly growing research field. This will be the highlight of this review. In a first part of this paper, a general introduction in the field of surface engineering will be given. Thereafter, we will focus on plasma-based strategies for surface modification. The purpose of the present review is twofold. First, we wish to provide a tutorial-type review that allows a fast introduction for researchers into the field. Second, we aim to give a comprehensive overview of recent work on surface modification of polymeric biomaterials, with a focus on plasma-based strategies. Some recent trends will be exemplified. On the basis of this literature study, we will conclude with some future trends for research.

  1. Formation of superpower volume discharges and their application for modification of surface of metals

    Science.gov (United States)

    Tarasenko, Victor F.; Shulepov, M. A.

    2008-05-01

    The results of experimental investigations of a volume avalanche discharge initiated by an e-beam (VADIEB) and surface layer of Cu and AlBe foils modifications at the plasma action of VADIEB are given. The volume discharge in the air of atmosphere pressure formed in the gap with the cathode having small curvature radius and with high voltage pulses of nanosecond duration and positive and negative polarity. A supershort avalanche electron beam (SAEB) with formation conditions in gases under atmospheric pressure have been investigated. It is proved that the surface layer is cleared of carbon at foil treatment, and atoms of oxygen penetrate into a foil. It is show that the cleaning depth depends on polarity of voltage pulses. At positive polarity of a copper foil electrode the cleaning is observed at the depth over 50 nm, and atoms of oxygen penetrate at the depth up to 25 nm. Plasma of the superpower volume discharge of nanosecond duration with a specific excitation power of hundreds of MW/cm3, and SAEB, and the discharge plasma radiation of various spectral ranges (including UV, VUV and X-ray) has the influence on the anode. The supershort avalanche electronic beam is generated only at negative polarity of a voltage pulse on an electrode with a small radius of curvature. SAEB influence on modifications of the copper foil surface is registered. VADIEB is easily realized in various gases and at various pressures, and, at gas pressure decrease the density of the beam current in helium can achieve 2 kA/cm2. It allows predicting an opportunity of VADIEB application for metal surface modifications in various technological processes, and for surface dielectric modifications at the certain design of the anode.

  2. Interaction of progenitor bone cells with different surface modifications of titanium implant

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Wen-Cheng, E-mail: wencchen@fcu.edu.tw [Advanced Medical Devices and Composites Laboratory, Department of Fiber and Composite Materials, College of Engineering, Feng Chia University, Taichung 40724, Taiwan (China); Chen, Ya-Shun [Advanced Medical Devices and Composites Laboratory, Department of Fiber and Composite Materials, College of Engineering, Feng Chia University, Taichung 40724, Taiwan (China); Ko, Chia-Ling [Advanced Medical Devices and Composites Laboratory, Department of Fiber and Composite Materials, College of Engineering, Feng Chia University, Taichung 40724, Taiwan (China); Dental Medical Devices and Materials Research Center, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan (China); Lin, Yi; Kuo, Tzu-Huang; Kuo, Hsien-Nan [Medical Device Development Division, Metal Industries Research and Development Centre, Kaohsiung 82151, Taiwan (China)

    2014-04-01

    Changes in the physical and chemical properties of Ti surfaces can be attributed to cell performance, which improves surface biocompatibility. The cell proliferation, mineralization ability, and gene expression of progenitor bone cells (D1 cell) were compared on five different Ti surfaces, namely, mechanical grinding (M), electrochemical modification through potentiostatic anodization (ECH), sandblasting and acid etching (SLA), sandblasting, hydrogen peroxide treatment, and heating (SAOH), and sandblasting, alkali heating, and etching (SMART). SAOH treatment produced the most hydrophilic surface, whereas SLA produced the most hydrophobic surface. Cell activity indicated that SLA and SMART produced significantly rougher surfaces and promoted D1 cell attachment within 1 day of culturing, whereas SAOH treatment produced moderate roughness (Ra = 1.26 μm) and accelerated the D1 cell proliferation up to 7 days after culturing. The ECH surface significantly promoted alkaline phosphatase (ALP) expression and osteocalcin (OCN) secretion in the D1 cells compared with the other surface groups. The ECH and SMART-treated Ti surfaces resulted in maximum ALP and OCN expressions during the D1 cell culture. SLA, SAOH, and SMART substrate surfaces were rougher and exhibited better cell metabolic responses during the early stage of cell attachment, proliferation, and morphologic expressions within 1 day of D1 cell culture. The D1 cells cultured on the ECH and SMART substrates exhibited higher differentiation, and higher ALP and OCN expressions after 10 days of culture. Thus, the ECH and SMART treatments promote better ability of cell mineralization in vitro, which demonstrate their great potential for clinical use. - Highlights: • Progenitor bone cells onto Ti with different modifications are characterized. • Surface roughness and hydrophilicity encourage early stage cell attachment. • Composition and surface treatments are more vital in bone cell mineralization.

  3. Preparation and Biocompatible Surface Modification of Redox Altered Cerium Oxide Nanoparticle Promising for Nanobiology and Medicine

    KAUST Repository

    Nanda, Himansu

    2016-11-03

    The biocompatible surface modification of metal oxide nanoparticles via surface functionalization technique has been used as an important tool in nanotechnology and medicine. In this report, we have prepared aqueous dispersible, trivalent metal ion (samarium)-doped cerium oxide nanoparticles (SmCNPs) as model redox altered CNPs of biological relevance. SmCNP surface modified with hydrophilic biocompatible (6-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-hexyl) triethoxysilane (MEEETES) were prepared using ammonia-induced ethylene glycol-assisted precipitation method and were characterized using a variety of complementary characterization techniques. The chemical interaction of functional moieties with the surface of doped nanoparticle was studied using powerful 13C cross polarization magic angle sample spinning nuclear magnetic resonance spectroscopy. The results demonstrated the production of the extremely small size MEEETES surface modified doped nanoparticles with significant reduction in aggregation compared to their unmodified state. Moreover, the functional moieties had strong chemical interaction with the surface of the doped nanoparticles. The biocompatible surface modification using MEEETES should also be extended to several other transition metal ion doped and co-doped CNPs for the production of aqueous dispersible redox altered CNPs that are promising for nanobiology and medicine.

  4. Surface modification of seawater desalination reverse osmosis membranes: Characterization studies & performance evaluation

    KAUST Repository

    Matin, Asif

    2014-06-01

    In this work we report surface modification of commercial reverse osmosis membranes by depositing ultrathin copolymer coatings, which could potentially enhance the biofouling resistance of RO membranes. Hydrophilic monomer hydroxyethyl methacrylate (HEMA) and a hydrophobic monomer, perfluorodecyl acrylate (PFDA) were copolymerized directly on the active layer of commercial aromatic polyamide reverse osmosis (RO) membranes using an initiated Chemical Vapor Deposition (iCVD) technique. Attenuated total reflective Fourier transform infrared spectra (ATR-FTIR) verified the successful modification of the membrane surfaces as a new FTIR adsorption band around 1730cm-1 corresponding to carbonyl groups in the copolymer film appeared after the deposition. X-ray Photoelectron spectroscopy (XPS) analysis also confirmed the presence of the copolymer film on the membrane surface by showing strong fluorine peaks emanating from the fluorinated alkyl side chains of the PFA molecules. Contact angle measurements with deionized water showed the modified membrane surfaces to be initially very hydrophobic but quickly assumed a hydrophilic character within few minutes. Atomic Force Microscopy (AFM) revealed that the deposited films were smooth and conformal as the surface topology of the underlying membrane surface remained virtually unchanged after the deposition. FESEM images of the top surface also showed that the typical ridge-and-valley structure associated with polyamide remained intact after the deposition. Short-term permeation tests using DI water and 2000ppm NaCl water showed that the deposited copolymer coatings had negligible effect on permeate water flux and salt rejection. © 2013 Elsevier B.V.

  5. Surface modification by allylamine plasma polymerization promotes osteogenic differentiation of human adipose-derived stem cells.

    Science.gov (United States)

    Liu, Xujie; Feng, Qingling; Bachhuka, Akash; Vasilev, Krasimir

    2014-06-25

    Tuning the material properties in order to control the cellular behavior is an important issue in tissue engineering. It is now well-established that the surface chemistry can affect cell adhesion, proliferation, and differentiation. In this study, plasma polymerization, which is an appealing method for surface modification, was employed to generate surfaces with different chemical compositions. Allylamine (AAm), acrylic acid (AAc), 1,7-octadiene (OD), and ethanol (ET) were used as precursors for plasma polymerization in order to generate thin films rich in amine (-NH2), carboxyl (-COOH), methyl (-CH3), and hydroxyl (-OH) functional groups, respectively. The surface chemistry was characterized by X-ray photoelectron spectroscopy (XPS), the wettability was determined by measuring the water contact angles (WCA) and the surface topography was imaged by atomic force microscopy (AFM). The effects of surface chemical compositions on the behavior of human adipose-derive stem cells (hASCs) were evaluated in vitro: Cell Count Kit-8 (CCK-8) analysis for cell proliferation, F-actin staining for cell morphology, alkaline phosphatase (ALP) activity analysis, and Alizarin Red S staining for osteogenic differentiation. The results show that AAm-based plasma-polymerized coatings can promote the attachment, spreading, and, in turn, proliferation of hASCs, as well as promote the osteogenic differentiation of hASCs, suggesting that plasma polymerization is an appealing method for the surface modification of scaffolds used in bone tissue engineering.

  6. Nitrogen ion implantation on stainless steel: AFM study of surface modification

    Energy Technology Data Exchange (ETDEWEB)

    Chico, B. [Dpto. Ingenieria de Materiales, Degradacion y Durabilidad, Centro Nacional de Investigaciones Metalurgicas (CENIM), CSIC, Avda. Gregorio del Amo, 8, 28040 Madrid (Spain)]. E-mail: bchico@cenim.csic.es; Martinez, L. [Dpto. Ciencia de los Materiales e Ingenieria Metalurgica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria, 28040 Madrid (Spain); Perez, F.J. [Dpto. Ciencia de los Materiales e Ingenieria Metalurgica, Facultad de Ciencias Quimicas, Universidad Complutense de Madrid, Ciudad Universitaria, 28040 Madrid (Spain)

    2005-04-30

    This work presents a study by means of atomic force microscopy (AFM) of the modification of the surface topography of AISI 304 austenitic stainless steel after N-ion implantation, irradiated by 1 x 10{sup 15} N{sub 2}{sup +}/cm{sup 2} at 80 keV. Prior to the implantation surface modification, the samples were electropolished for the optimum observation of the surface at a small scale to obtain an initial surface with the smaller roughness. The electrolytic bath was composed of a mixture of water/sulphuric acid/orthophosphoric acid in percentages 20, 20 and 60%, respectively. Once the surface was optimized, the samples were implanted and observed by AFM, a new technique whose importance relies on its resolution power, allowing the acquisition of topographic images of the surface with nanometric resolution. Thanks to the high resolution power could be observed that ion implantation increases the surface roughness and promotes the apparition of 3 {mu}m wide and 10 nm depth craters as well as the apparition of products with singular morphology.

  7. Structural and compositional modification of a barium boroaluminosilicate glass surface by thermal poling

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Nicholas J. [The Pennsylvania State University, Department of Material Science and Engineering, Materials Research Institute, University Park, PA (United States); Science and Technology Division, Corning Incorporated, Corning, NY (United States); Pantano, Carlo G. [The Pennsylvania State University, Department of Material Science and Engineering, Materials Research Institute, University Park, PA (United States)

    2014-08-15

    In addition to inducing second-order nonlinear properties, significant structural and compositional alteration can be imparted to glass surfaces during the process of thermal poling. In this work, we focus on how thermal poling affects a structurally complex, nominally alkali-free boroaluminosilicate display glass composition. We provide evidence for electrolysis of the glass network, characterized by the migration of both cations (Ba{sup 2+}, Na{sup +}) and anions (O{sup -}, F{sup -}) towards opposing electrode interfaces. This process results in oxidation of the positively biased electrode and forms a network-former rich, modifier-depleted glass surface layer adjacent to the anodic interface. The modified glass layer thickness is qualitatively correlated to the oxidation resistance of the electrode material, while extrinsic ions such as H{sup +}/H{sub 3}O{sup +} at not found in the depletion layer to compensate for the migration of modifier cations out of the region. Rather, FTIR spectroscopy suggests a local restructuring of the B{sub 2}O{sub 3}-Al{sub 2}O{sub 3}-SiO{sub 2} network species to accommodate the charge imbalance created by the exodus of network-modifying cations, specifically the conversion of tetrahedral B(4) to trigonal B(3) as Ba or Na ions are removed from B-related sites in the parent network. The resultant poling-induced depletion layer exhibits enhanced hydrolytic resistance under acidic conditions, and the IR spectra are substantially unlike those produced by acid leaching the same glass. (orig.)

  8. Surface modifications of photoanodes in dye sensitized solar cells: enhanced light harvesting and reduced recombination

    Science.gov (United States)

    Saxena, Vibha; Aswal, D. K.

    2015-06-01

    In a quest to harvest solar power, dye-sensitized solar cells (DSSCs) have potential for low-cost eco-friendly photovoltaic devices. The major processes which govern the efficiency of a DSSC are photoelectron generation, injection of photo-generated electrons to the conduction band (CB) of the mesoporous nanocrystalline semiconductor (nc-SC); transport of CB electrons through nc-SC and subsequent collection of CB electrons at the counter electrode (CE) through the external circuit; and dye regeneration by redox couple or hole transport layer (HTL). Most of these processes occur at various interfaces of the photoanode. In addition, recombination losses of photo-generated electrons with either dye or redox molecules take place at the interfaces. Therefore, one of the key requirements for high efficiency is to improve light harvesting of the photoanode and to reduce the recombination losses at various interfaces. In this direction, surface modification of the photoanode is the simplest method among the various other approaches available in the literature. In this review, we present a comprehensive discussion on surface modification of the photoanode, which has been adopted in the literature for not only enhancing light harvesting but also reducing recombination. Various approaches towards surface modification of the photoanode discussed are (i) fluorine-doped tin oxide (FTO)/nc-SC interface modified via a compact layer of semiconductor material which blocks exposed sites of FTO to electrolyte (or HTL), (ii) nc-SC/dye interface modification either through acid treatment resulting in enhanced dye loading due to a positively charged surface or by depositing insulating/semiconducting blocking layer on the nc-SC surface, which acts as a tunneling barrier for recombination, (iii) nc-SC/dye interface modified by employing co-adsorbents which helps in reducing the dye aggregation and thereby recombination, and (iv) dye/electrolyte (or dye/HTL) interface modification using

  9. Surface modification and property analysis of biomedical polymers used for tissue engineering.

    Science.gov (United States)

    Ma, Zuwei; Mao, Zhengwei; Gao, Changyou

    2007-11-15

    The response of host organism in macroscopic, cellular and protein levels to biomaterials is, in most cases, closely associated with the materials' surface properties. In tissue engineering, regenerative medicine and many other biomedical fields, surface engineering of the bio-inert synthetic polymers is often required to introduce bioactive species that can promote cell adhesion, proliferation, viability and enhanced ECM-secretion functions. Up to present, a large number of surface engineering techniques for improving biocompatibility have been well established, the work of which generally contains three main steps: (1) surface modification of the polymeric materials; (2) chemical and physical characterizations; and (3) biocompatibility assessment through cell culture. This review focuses on the principles and practices of surface engineering of biomedical polymers with regards to particular aspects depending on the authors' research background and opinions. The review starts with an introduction of principles in designing polymeric biomaterial surfaces, followed by introduction of surface modification techniques to improve hydrophilicity, to introduce reactive functional groups and to immobilize functional protein molecules. The chemical and physical characterizations of the modified biomaterials are then discussed with emphasis on several important issues such as surface functional group density, functional layer thickness, protein surface density and bioactivity. Three most commonly used surface composition characterization techniques, i.e. ATR-FTIR, XPS, SIMS, are compared in terms of their penetration depth. Ellipsometry, CD, EPR, SPR and QCM's principles and applications in analyzing surface proteins are introduced. Finally discussed are frequently applied methods and their principles to evaluate biocompatibility of biomaterials via cell culture. In this section, current techniques and their developments to measure cell adhesion, proliferation, morphology

  10. Surface Modification of Carbon Nanotubes with Conjugated Polyelectrolytes: Fundamental Interactions and Applications in Composite Materials, Nanofibers, Electronics, and Photovoltaics

    KAUST Repository

    Ezzeddine, Alaa

    2015-10-01

    Ever since their discovery, Carbon nanotubes (CNTs) have been renowned to be potential candidates for a variety of applications. Nevertheless, the difficulties accompanied with their dispersion and poor solubility in various solvents have hindered CNTs potential applications. As a result, studies have been developed to address the dispersion problem. The solution is in modifying the surfaces of the nanotubes covalently or non-covalently with a desired dispersant. Various materials have been employed for this purpose out of which polymers are the most common. Non-covalent functionalization of CNTs via polymer wrapping represents an attractive method to obtain a stable and homogenous CNTs dispersion. This method is able to change the surface properties of the nanotubes without destroying their intrinsic structure and preserving their properties. This thesis explores and studies the surface modification and solublization of pristine single and multiwalled carbon nanotubes via a simple solution mixing technique through non-covalent interactions of CNTs with various anionic and cationic conjugated polyelectrolytes (CPEs). The work includes studying the interaction of various poly(phenylene ethynylene) electrolytes with MWCNTs and an imidazolium functionalized poly(3-hexylthiophene) with SWCNTs. Our work here focuses on the noncovalent modifications of carbon nanotubes using novel CPEs in order to use these resulting CPE/CNT complexes in various applications. Upon modifying the CNTs with the CPEs, the resulting CPE/CNT complex has been proven to be easily dispersed in various organic and aqueous solution with excellent homogeneity and stability for several months. This complex was then used as a nanofiller and was dispersed in another polymer matrix (poly(methyl methacrylate), PMMA). The PMMA/CPE/CNT composite materials were cast or electrospun depending on their desired application. The presence of the CPE modified CNTs in the polymer matrix has been proven to enhance

  11. Synthesis, Phase Transfer and Surface Modification of Hydrophobic Quantum Dots for Bioapplications

    Science.gov (United States)

    Zhang, Ruili; Zhang, Xiao; Li, Xiaoyu; Yang, Ping

    2013-04-01

    We review the preparation, phase transfer, surface modification and possible bioapplications of hydrophobic CdSe based quantum dots (QDs). CdSe cores with rod and spherical morphologies were prepared through adjusting preparation conditions. The photoluminescence (PL) of the QDs depended strongly on preparation conditions. The QDs were coated with semiconductor shells to improve their PL properties. Anisotropic growth occurred during shell coating. Core/shell QDs revealed tunable PL and high PL efficiencies up to 90%. The phase transfer of QDs from oil phase to water phase was carried out via polymer or a sol-gel process. The silanization of the QDs plays an important role for the sol-gel process. Because of a SiO2 coating, the surface modification of the QDs for bioapplications became easy. After transferring into water phase, the QDs still retained high PL efficiency. Because of their high PL, these biofunctional materials could provide a platform for various applications.

  12. Solid-core and hollow magnetic nanostructures: Synthesis, surface modifications and biological applications.

    Science.gov (United States)

    Nieciecka, Dorota; Nawara, Krzysztof; Kijewska, Krystyna; Nowicka, Anna M; Mazur, Maciej; Krysinski, Pawel

    2013-10-01

    In the need of development of versatile and flexible platforms for sensing, nanostructured particles are one of the systems of choice. Additionally, the state-of-the-art, controlled surface modifications of these structures offer broad possibilities of using such systems for diagnostics and therapy, often referred to as thera(g)nostics. In this brief review we will focus on the synthesis and surface modifications of solid-core magnetic nanostructures and polymeric capsules containing nanoferrites modified with anti-cancer drug--doxorubicin, designed for magnetic field-driven drug delivery for cancer therapy. We will also outline some problems related to the usage of such structures. The encapsulation and distribution of magnetic iron oxide nanoparticles modified with doxorubicin will be demonstrated in the polypyrrole spherical microvessels.

  13. Recent advances in synthesis and surface modification of superparamagnetic iron oxide nanoparticles with silica

    Energy Technology Data Exchange (ETDEWEB)

    Sodipo, Bashiru Kayode, E-mail: bashirsodipo@gmail.com [School of Physics, Universiti Sains Malaysia, 11800 Pulau Pinang (Malaysia); Nano-Biotechnology Research and Innovation (NanoBRI), Institute for Research in Molecular Medicine (INFORMM), Universiti Sains Malaysia, 11800 Pulau Pinang (Malaysia); Aziz, Azlan Abdul [School of Physics, Universiti Sains Malaysia, 11800 Pulau Pinang (Malaysia); Nano-Biotechnology Research and Innovation (NanoBRI), Institute for Research in Molecular Medicine (INFORMM), Universiti Sains Malaysia, 11800 Pulau Pinang (Malaysia)

    2016-10-15

    Research on synthesis of superparamagnetic iron oxide nanoparticles (SPION) and its surface modification for biomedical applications is of intense interest. Due to superparamagnetic property of SPION, the nanoparticles have large magnetic susceptibility, single magnetic domain and controllable magnetic behaviour. However, owing to easy agglomeration of SPION, surface modification of the magnetic particles with biocompatible materials such as silica nanoparticle has gained much attention in the last decade. In this review, we present recent advances in synthesis of SPION and various routes of producing silica coated SPION. - Highlights: • We present recent advances in synthesis of SPION and various routes of producing silica coated SPION • The synthetic routes of producing SPION can be classified into three: physical, chemical and biological methods. • The chemical method is the most cited method of producing SPION and it sub-classified into liquid and gas phase. • The techniques of producing silica coated SPION is grouped into seeded and non-seeded methods.

  14. Nanoscale surface modification for enhanced biosensing a journey toward better glucose monitoring

    CERN Document Server

    Zhang, Guigen

    2015-01-01

    This book gives a comprehensive overview of electrochemical-based biosensors and their crucial components. Practical examples are given throughout the text to illustrate how the performance of electrochemical-based biosensors can be improved by nanoscale surface modification and how an optimal design can be achieved. All essential aspects of biosensors are considered, including electrode functionalization, efficiency of the mass transport of reactive species, and long term durability and functionality of the sensor. This book also: ·       Explains how the performance of an electrochemical-based biosensor can be improved by nanoscale surface modification ·       Gives readers the tools to evaluate and improve the performance of a biosensor with a multidisciplinary approach that considers electrical, electrostatic, electrochemical, chemical, and biochemical events ·       Links the performance of a sensor to the various governing physical and chemical principles so readers can fully unders...

  15. The third generation multi-purpose plasma immersion ion implanter for surface modification of materials

    CERN Document Server

    Tang Bao Yin; Wang Xiao Feng; Gan Kong Yin; Wang Song Yan; Chu, P K; Huang Nian Ning; Sun Hong

    2002-01-01

    The third generation multi-purpose plasma immersion ion implantation (PIII) equipment has been successfully used for research and development of surface modification of biomedical materials, metals and their alloys in the Southwest Jiaotong University. The implanter equipped with intense current, pulsed cathodic arc metal plasma sources which have both strong coating function and gas and metal ion implantation function. Its pulse high voltage power supply can provide big output current. It can acquire very good implantation dose uniformity. The equipment can both perform ion implantation and combine ion implantation with sputtering deposition and coating to form many kinds of synthetic surface modification techniques. The main design principles, features of important components and achievement of research works in recent time have been described

  16. Surface modification of hydroxyapatite nanocrystals by grafting polymers containing phosphonic acid groups.

    Science.gov (United States)

    Choi, Hyung Woo; Lee, Hong Jae; Kim, Kyung Ja; Kim, Hyun-Min; Lee, Sang Cheon

    2006-12-01

    A novel approach for the surface modification of hydroxyapatite (HAp) nanocrystals is described by grafting polymerization of vinyl phosphonic acid (VPA) using a redox initiating system in an aqueous media. Fourier transform infrared (FT-IR) and XRD analyses confirmed the modification reaction on HAp surfaces. Inductively coupled plasma mass spectroscopy (ICP MS) showed that the Ca/P molar ratio decreased from 1.67 to 1.36 with increasing the feed VPA amount. Zeta potentials of unmodified HAp and modified HAp in phosphate-buffered saline (PBS) solutions (pH 7.4, ionic strength = 10 mM) were negative and decreased with increasing the amount of grafted PVPA. Transmission electron microscopy (TEM) measurements and time-dependent phase monitoring indicated that the colloidal stability of modified HAp over unmodified HAp in water dramatically increased and tended to exist as single nanocrystals without aggregation.

  17. Competition Between Organic Matter and Solid Surface for Cation Sorption: Ce and Rare Earth Element as Proxy

    Science.gov (United States)

    Davranche, M.; Pourret, O.; Gruau, G.; Dia, A.

    2006-12-01

    Aquatic or soil organic matter are well-known to be strong adsorbent of many cations due to their adsorption capacity. Among these cations, the trivalent rare earth element (REE) and particularly Ce seem to be promising tools to investigate the impact of competition in between organic or inorganic ligands. Ce (III) is oxidized into Ce (IV) by oxidative surface such as Fe and Mn oxyhydroxides. Since Ce (IV) is preferentially adsorbed (as compared to other REE), a positive and negative Ce anomaly is developed respectively onto the solid and within the solution. Previous studies (Davranche et al., 2004, 2005) highlighted the suppression of this feature when Ce occurs to be complexed with organic matter (as humate species). Recent experiments were designed to evaluate the competition between humate and Mn oxide for REE complexation (each reactant being added simultaneously). Two parameters control the competition: time and pH. While organic matter does adsorb immediately the free REE, a desorption of REE occurs through time. Desorption is marked by the development of a Ce anomaly in the REE pattern that reflects the complexation with Mn oxide surface. Along the time, solid surface becomes thus more competitive than the organic matter. PH still influences the competition since at basic pH, REE and organic matter - probably as REE-organic complexes - are adsorbed onto the solid surface. Ultrafiltration analyses at 5 KD were also performed to separate organic matter and organic complexes from the solution. Results provide evidence that in presence of a solid surface, HREE (high rare earth element) desorption from the organic matter occurs through time. This leads to HREE enrichment in solution. All these results suggest that complexation of organic matter is kinetically favoured as compared to the complexation with solid surfaces. However, the organic complex formed during the first stage of the complexation process involves weak bindings. These bindings are easily broken

  18. Protein Adsorption to Surface Chemistry and Crystal Structure Modification of Titanium Surfaces

    Directory of Open Access Journals (Sweden)

    Ryo Jimbo

    2010-07-01

    Full Text Available Objectives: To observe the early adsorption of extracellular matrix and blood plasma proteins to magnesium-incorporated titanium oxide surfaces, which has shown superior bone response in animal models.Material and Methods: Commercially pure titanium discs were blasted with titanium dioxide (TiO2 particles (control, and for the test group, TiO2 blasted discs were further processed with a micro-arc oxidation method (test. Surface morphology was investigated by scanning electron microscopy, surface topography by optic interferometry, characterization by X-ray photoelectron spectroscopy (XPS, and by X-ray diffraction (XRD analysis. The adsorption of 3 different proteins (fibronectin, albumin, and collagen type I was investigated by an immunoblotting technique.Results: The test surface showed a porous structure, whereas the control surface showed a typical TiO2 blasted structure. XPS data revealed magnesium-incorporation to the anodic oxide film of the surface. There was no difference in surface roughness between the control and test surfaces. For the protein adsorption test, the amount of albumin was significantly higher on the control surface whereas the amount of fibronectin was significantly higher on the test surface. Although there was no significant difference, the test surface had a tendency to adsorb more collagen type I.Conclusions: The magnesium-incorporated anodized surface showed significantly higher fibronectin adsorption and lower albumin adsorption than the blasted surface. These results may be one of the reasons for the excellent bone response previously observed in animal studies.

  19. High-productivity membrane adsorbers: Polymer surface-modification studies for ion-exchange and affinity bioseparations

    Science.gov (United States)

    Chenette, Heather C. S.

    This dissertation centers on the surface-modification of macroporous membranes to make them selective adsorbers for different proteins, and the analysis of the performance of these membranes relative to existing technology. The common approach used in these studies, which is using membrane technology for chromatographic applications and using atom transfer radical polymerization (ATRP) as a surface modification technique, will be introduced and supported by a brief review in Chapter 1. The specific approaches to address the unique challenges and motivations of each study system are given in the introduction sections of the respective dissertation chapters. Chapter 2 describes my work to develop cation-exchange membranes. I discuss the polymer growth kinetics and characterization of the membrane surface. I also present an analysis of productivity, which measures the mass of protein that can bind to the stationary phase per volume of stationary phase adsorbing material per time. Surprisingly and despite its importance, this performance measure was not described in previous literature. Because of the significantly shorter residence time necessary for binding to occur, the productivity of these cation-exchange membrane adsorbers (300 mg/mL/min) is nearly two orders of magnitude higher than the productivity of a commercial resin product (4 mg/mL/min). My work studying membrane adsorbers for affinity separations was built on the productivity potential of this approach, as articulated in the conclusion of Chapter 2. Chapter 3 focuses on the chemical formulation work to incorporate glycoligands into the backbone of polymer tentacles grown from the surface of the same membrane stationary phase. Emphasis is given to characterizing and testing the working formulation for ligand incorporation, and details about how I arrived at this formulation are given in Appendix B. The plant protein, or lectin, Concanavalin A (conA) was used as the target protein. The carbohydrate affinity

  20. Biodegradable Magnesium Alloys for Orthopaedic Applications: A Review on Corrosion, Biocompatibility and Surface Modifications.

    OpenAIRE

    Agarwal, Sankalp; Curtin, James; Duffy, Brendan; Jaiswal, Swarna

    2016-01-01

    Magnesium (Mg) and its alloys have been extensively explored as potential biodegradable implant materials for orthopaedic applications (e.g. Fracture fixation). However, the rapid corrosion of Mg based alloys in physiological conditions has delayed their introduction for therapeutic applications to date. The present review focuses on corrosion, biocompatibility and surface modifications of biodegradable Mg alloys for orthopaedic applications. Initially, the corrosion behaviour of Mg alloys an...

  1. Experimental Study on the Surface Modification of Ultra Thin DLC Films

    Institute of Scientific and Technical Information of China (English)

    ZHU Shou-xing; ZHU Shi-gen

    2005-01-01

    School of Mechanical Engineering, Donghua University, Shanghai 200051Surface modification of Diamond-like carbon (DLC) films was carried out in order to estimate the reliability of the ultra thin DLC films. The wear resistance, conductivity and mechatronic reliability of the films were studied by contact atomic force microscope (AFM), electric force microscope (EFM) and conductive AFM. The failure mechanism of pits formed and the reason for conductivity changed of DLC films were examined.

  2. Surface Modification Of The High Temperature Porous Sliding Bearings With Solid Lubricant Nanoparticles

    OpenAIRE

    2015-01-01

    A surface modification of stainless steel bearing sleeves is developed to improve the tribology characteristics at high temperature. Solid lubricant nano- and microparticles are applied for this purpose. To create the quasi-hydrodynamic lubrication regimes, the solid lubricant powder layer is made by developed pressure impregnation technique. Porous sliding bearing sleeve prototypes were made by powder metallurgy technique. The purpose of the paper is to define the friction and wear character...

  3. Surface Modification of Electrospun PVDF/PAN Nanofibrous Layers by Low Vacuum Plasma Treatment

    OpenAIRE

    Fatma Yalcinkaya; Baturalp Yalcinkaya; Adam Pazourek; Jana Mullerova; Martin Stuchlik; Jiri Maryska

    2016-01-01

    Nanofibres are very promising for water remediation due to their high porosity and small pore size. Mechanical properties of nanofibres restrict the application of pressure needed water treatments. Various PAN, PVDF, and PVDF/PAN nanofibre layers were produced, and mechanical properties were improved via a lamination process. Low vacuum plasma treatment was applied for the surface modification of nanofibres. Atmospheric air was used to improve hydrophilicity while sulphur hexafluoride gas was...

  4. Surface Modification Counteracts Adverse Effects Associated with Immobilization after Flexor Tendon Repair

    OpenAIRE

    2012-01-01

    Although post-rehabilitation is routinely performed following flexor tendon repair, in some clinical scenarios post-rehabilitation must be delayed. We investigated modification of the tendon surface using carbodiimide derivatized hyaluronic acid and lubricin (cd-HA-Lub) to maintain gliding function following flexor tendon repair with postoperative immobilization in a in vivo canine model. Flexor digitorum profundus tendons from the 2nd and 5th digits of one forepaw of six dogs were transected...

  5. Surface modification to improve fireside corrosion resistance of Fe-Cr ferritic steels

    Science.gov (United States)

    Park, Jong-Hee; Natesan, Krishnamurti; Rink, David L.

    2010-03-16

    An article of manufacture and a method for providing an Fe--Cr ferritic steel article of manufacture having a surface layer modification for corrosion resistance. Fe--Cr ferritic steels can be modified to enhance their corrosion resistance to liquid coal ash and other chemical environments, which have chlorides or sulfates containing active species. The steel is modified to form an aluminide/silicide passivating layer to reduce such corrosion.

  6. Surface modifications and Nano-composite coatings to improve the bonding strength of titanium-porcelain.

    Science.gov (United States)

    Guo, Litong; Chen, Xiaoyuan; Liu, Xuemei; Feng, Wei; Li, Baoe; Lin, Cheng; Tao, Xueyu; Qiang, Yinghuai

    2016-04-01

    Surface modifications of Ti and nano-composite coatings were employed to simultaneously improve the surface roughness, corrosion resistance and chemical bonding between porclain-Ti. The specimens were studied by field-emission scanning electron microscopy, surface roughness, differential scanning calorimetry, Fourier transform infrared spectroscopy, corrosion resistance and bonding strength tests. The SEM results showed that hybrid structures with micro-stripes, nano-pores and nano-protuberances were prepared by surface modification of Ti, which significantly enhanced the surface roughness and corrosion resistance of Ti. Porous nano-composite coatings were synthesized on Ti anodized with pre-treatment in 40% HF acid. TiO2 nanoparticles were added into the hybrid coating to increase the solid phase content of the sols and avoid the formation of microcracks. With the TiO2 content increasing from 45 wt% to 60 wt%, the quantities of the microcracks on the coating surface gradually decreased. The optimal TiO2 content for the nanocomposite coatings is 60 wt% in this research. Compared to the uncoated group, the bonding strength of the coated groups showed a bonding strength improvement of 23.96%. The cytotoxicity of the 4# coating group was ranked as zero, which corresponds to non-cytotoxicity.

  7. Modification of a metallic surface in a vacuum arc discharge plasma using thermally stimulated ion diffusion

    Science.gov (United States)

    Muboyadzhyan, S. A.

    2008-12-01

    A new process for modifying a metallic surface in a vacuum arc discharge plasma using thermally stimulated ion diffusion is considered. The effect of the bias voltage (negative substrate potential) on the processes that occur on the surface of a treated part is studied when the substrate material interacts with an accelerated metallic-ion flow. The phase and elemental compositions of the modified layer are studied for substrates made of nickel-based superalloys, austenitic and martensitic steels, and titanium-based alloys. The heat resistance, the salt corrosion resistance, and the corrosion cracking resistance of steels and titanium-based alloys are investigated after their modification in vacuum arc plasmas of pure metals (Ti, Zr, Al, Cr, Y) and related alloys. The surface modification caused by the thermally stimulated ion saturation of the surfaces of parts made from structural materials is shown to change the structural-phase states of their surfaces and, correspondingly, the properties of these materials in relation to the state of the surface.

  8. Surface modification of electrospun fibres for biomedical applications: A focus on radical polymerization methods.

    Science.gov (United States)

    Duque Sánchez, Lina; Brack, Narelle; Postma, Almar; Pigram, Paul J; Meagher, Laurence

    2016-11-01

    The development of electrospun ultrafine fibres from biodegradable and biocompatible polymers has created exciting opportunities for biomedical applications. Fibre meshes with high surface area, suitable porosity and stiffness have been produced. Despite desirable structural and topographical properties, for most synthetic and some naturally occurring materials, the nature of the fibre surface chemistry has inhibited development. Hydrophobicity, undesirable non-specific protein adsorption and bacterial attachment and growth, coupled with a lack of surface functionality in many cases and an incomplete understanding of the myriad of interactions between cells and extracellular matrix (ECM) proteins have impeded the application of these systems. Chemical and physical treatments have been applied in order to modify or control the surface properties of electrospun fibres, with some success. Chemical modification using controlled radical polymerization, referred to here as reversible-deactivation radical polymerization (RDRP), has successfully introduced advanced surface functionality in some fibre systems. Atom transfer radical polymerization (ATRP) and reversible addition fragmentation chain transfer (RAFT) are the most widely investigated techniques. This review analyses the practical applications of electrospinning for the fabrication of high quality ultrafine fibres and evaluates the techniques available for the surface modification of electrospun ultrafine fibres and includes a detailed focus on RDRP approaches.

  9. Enhancing the Properties of Carbon and Gold Substrates by Surface Modification

    Energy Technology Data Exchange (ETDEWEB)

    Jennifer Anne Harnisch

    2002-06-27

    The properties of both carbon and gold substrates are easily affected by the judicious choice of a surface modification protocol. Several such processes for altering surface composition have been published in literature. The research presented in this thesis primarily focuses on the development of on-column methods to modify carbon stationary phases used in electrochemically modulated liquid chromatography (EMLC). To this end, both porous graphitic carbon (PGC) and glassy carbon (GC) particles have been modified on-column by the electroreduction of arenediazonium salts and the oxidation of arylacetate anions (the Kolbe reaction). Once modified, the carbon stationary phases show enhanced chromatographic performance both in conventional liquid chromatographic columns and EMLC columns. Additionally, one may also exploit the creation of aryl films to by electroreduction of arenediazonium salts in the creation of nanostructured materials. The formation of mercaptobenzene film on the surface of a GC electrode provides a linking platform for the chemisorption of gold nanoparticles. After deposition of nanoparticles, the surface chemistry of the gold can be further altered by self-assembled monolayer (SAM) formation via the chemisorption of a second thiol species. Finally, the properties of gold films can be altered such that they display carbon-like behavior through the formation of benzenehexathiol (BHT) SAMs. BHT chemisorbs to the gold surface in a previously unprecedented planar fashion. Carbon and gold substrates can be chemically altered by several methodologies resulting in new surface properties. The development of modification protocols and their application in the analytical arena is considered herein.

  10. Effect of coating and surface modification on the corrosion resistance of selected alloys in supercritical water

    Energy Technology Data Exchange (ETDEWEB)

    Li, J.; Zheng, W. [CANMET, Materials Technology Lab., Hamilton, Ontario (Canada); Cook, W. [Univ. of New Brunswick, Fredericton, New Brunswick (Canada); Toivonen, A.; Penttila, S. [VTT Technical Research Center of Finland, Espoo (Finland); Guzonas, D.; Woo, O.T. [Atomic Energy of Canada Limited, Chalk River, Ontario (Canada); Liu, P.; Bibby, D. [CANMET, Materials Technology Lab., Hamilton, Ontario (Canada)

    2011-07-01

    Materials selection is one of the key tasks in Gen-IV reactor development. There is no known material that can meet the expected core outlet conditions of the Canadian SCWR concept (625{sup o}C core outlet temperature). High-Cr steels with excellent corrosion resistance are often susceptible to embrittlement due to the precipitation of sigma and other phases in the microstructure. Low-Cr steels such as P91 and oxide dispersion strengthened (ODS) steels exhibit good high-temperature mechanical properties, but the lack of sufficient Cr content makes this group alloy corrode too fast. Improvement in this alloy is needed in order for it to be considered as a piping construction material. In this report, the development of a metallic coating on a P91 substrate is discussed. Recent effort on selection of in-core cladding alloys has focused on heat-resistant 3xx series stainless steels. These alloys have higher strength at high-temperature ranges, but corrosion and stress-corrosion cracking resistance are a concern. Metallic coating and surface modification are considered as possible solutions to overcome this challenge. The effects of surface modification on the corrosion rate of austenitic steels were also reported in this paper. As-machined surface showed much better corrosion resistance than polished surface and advanced surface analyses showed distinct differences in the nature and the morphology of the surface layer metal. Possible mechanisms for improved corrosion performance are discussed. (author)

  11. Surface modification of coconut shell based activated carbon for the improvement of hydrophobic VOC removal.

    Science.gov (United States)

    Li, Lin; Liu, Suqin; Liu, Junxin

    2011-08-30

    In this study, coconut shell based carbons were chemically treated by ammonia, sodium hydroxide, nitric acid, sulphuric acid, and phosphoric acid to determine suitable modification for improving adsorption ability of hydrophobic volatile organic compounds (VOCs) on granular activated carbons (GAC). The saturated adsorption capacities of o-xylene, a hydrophobic volatile organic compound, were measured and adsorption effects of the original and modified activated carbons were compared. Results showed that GAC modified by alkalis had better o-xylene adsorption capacity. Uptake amount was enhanced by 26.5% and reduced by 21.6% after modification by NH(3)H(2)O and H(2)SO(4), respectively. Compared with the original, GAC modified by acid had less adsorption capacity. Both SEM/EDAX and BET were used to identify the structural characteristics of the tested GAC, while IR spectroscopy and Boehm's titration were applied to analysis the surface functional groups. Relationships between physicochemical characteristics of GAC and their adsorption performances demonstrated that o-xylene adsorption capacity was related to surface area, pore volume, and functional groups of the GAC surface. Removing surface oxygen groups, which constitute the source of surface acidity, and reducing hydrophilic carbon surface favors adsorption capacity of hydrophobic VOCs on carbons. The performances of modified GACs were also investigated in the purification of gases containing complex components (o-xylene and steam) in the stream.

  12. Enhancing the Properties of Carbon and Gold Substrates by Surface Modification

    Energy Technology Data Exchange (ETDEWEB)

    Harnisch, Jennifer Anne [Iowa State Univ., Ames, IA (United States)

    2001-01-01

    The properties of both carbon and gold substrates are easily affected by the judicious choice of a surface modification protocol. Several such processes for altering surface composition have been published in literature. The research presented in this thesis primarily focuses on the development of on-column methods to modify carbon stationary phases used in electrochemically modulated liquid chromatography (EMLC). To this end, both porous graphitic carbon (PGC) and glassy carbon (GC) particles have been modified on-column by the electroreduction of arenediazonium salts and the oxidation of arylacetate anions (the Kolbe reaction). Once modified, the carbon stationary phases show enhanced chromatographic performance both in conventional liquid chromatographic columns and EMLC columns. Additionally, one may also exploit the creation of aryl films to by electroreduction of arenediazonium salts in the creation of nanostructured materials. The formation of mercaptobenzene film on the surface of a GC electrode provides a linking platform for the chemisorption of gold nanoparticles. After deposition of nanoparticles, the surface chemistry of the gold can be further altered by self-assembled monolayer (SAM) formation via the chemisorption of a second thiol species. Finally, the properties of gold films can be altered such that they display carbon-like behavior through the formation of benzenehexathiol (BHT) SAMs. BHT chemisorbs to the gold surface in a previously unprecedented planar fashion. Carbon and gold substrates can be chemically altered by several methodologies resulting in new surface properties. The development of modification protocols and their application in the analytical arena is considered herein.

  13. Silicon surface modifications produced by non-equilibrium He, Ne and Kr plasma jets

    Science.gov (United States)

    Engelhardt, Max; Kartaschew, Konstantin; Bibinov, Nikita; Havenith, Martina; Awakowicz, Peter

    2017-01-01

    In this publication the interaction of non-equilibrium plasma jets (N-APPJs) with silicon surfaces is studied. The N-APPJs are operated with He, Ne and Kr gas flows under atmospheric pressure conditions. Plasma bullets are produced by the He and Ne N-APPJs, while a filamentary discharge is ignited in the Kr flow. All these N-APPJs produce remarkable traces on silicon wafer surfaces treated in their effluents. Different types of etching tracks, blisters and crystals are observed on the treated surfaces. The observed traces and surface modifications of silicon wafers are analyzed with optical, atomic-force, scanning electron and Raman microscopes. Based on the material composition within the etching tracks and the position and dimension of blisters and crystals, the traces observed on the silicon wafer surfaces are interpreted as traces of micro-plasmoids. Amorphous silicon is found in the etching tracks. Blisters are produced through the formation of cracks inside the silicon crystal by the interaction with micro-plasmoids. The reason for these modifications is not clear now. The density of micro-plasmoids traces on the treated silicon surface and the depth and length of the etching tracks depends strongly on the type of the used carrier gas of the N-APPJ.

  14. Electrochemical impedance spectroscopy for graphene surface modification and protein translocation through the chemically modified graphene nanopore

    Science.gov (United States)

    Tiwari, Purushottam; Shan, Yuping; Wang, Xuewen; Darici, Yesim; He, Jin

    2014-03-01

    The multilayer graphene surface has been modified using mercaptohexadecanoic acid (MHA) and 1,2-dimyristoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-750] (DPPE-PEG750). The surface modifications are evaluated using electrochemical impedance spectroscopy (EIS). EIS measurements show the better graphene surface passivation with DPPE-PEG750 than with MHA. After modification with ferritin, the MHA modified surface shows greater charge transfer resistance (Rct) change than DPPE-PEG750 modified surface. Based on these results the translocations of ferritin through modified graphene nanopore with diameter 5-20 nm are studied. The translocation is more successful through DPPE-PEG750 modified graphene nanopore. This concludes that that the attachment of ferritin to DPPE-PEG750 modified graphene nanopore is not significant compared to MHA modified pore for the ferritin translocation hindrance. These results nicely correlate with the EIS data for respective Rct change of ferritin modified surfaces. P. Tiwari would like to thank FIU School of Integrated Science & Humanity, College Arts & Sciences for the research assistantship.

  15. Synthesis, surface properties and oil solubilisation capacity of cationic gemini surfactants

    NARCIS (Netherlands)

    Dam, Th.; Engberts, J.B.F.N.; Karthäuser, J.; Karaborni, S.; Os, N.M. van

    1996-01-01

    The critical micelle concentration (CMC) and the surface tension at the CMC have been determined for the gemini surfactants alkanediyl-u,w-bis(dimethyla1kylammoniubmr omide) by means of dynamic surface tension measurements. For the same number of carbon atoms in the hydrophobic chain per hydrophilic

  16. Surface modification and enhanced photocatalytic CO2 reduction performance of TiO2: a review

    Science.gov (United States)

    Low, Jingxiang; Cheng, Bei; Yu, Jiaguo

    2017-01-01

    Recently, the excessive consumption of fossil fuels has caused high emissions of the greenhouse gases, CO2 into atmosphere and global energy crisis. Mimicking the natural photosynthesis by using semiconductor materials to achieve photocatalytic CO2 reduction into valuable solar fuels such as CH4, HCO2H, CH2O, and CH3OH is known as one of the best solutions for addressing the aforementioned issue. Among various proposed photocatalysts, TiO2 has been extensively studied over the past several decades for photocatalytic CO2 reduction because of its cheapness and environmental friendliness. Particularly, surface modification of TiO2 has attracted numerous interests due to its capability of enhancing the light absorption ability, facilitating the electron-hole separation, tuning the CO2 reduction selectivity and increasing the CO2 adsorption and activation ability of TiO2 for photocatalytic CO2 reduction. In this review, recent approaches of the surface modification of TiO2 for photocatalytic CO2 reduction, including impurity doping, metal deposition, alkali modification, heterojunction construction and carbon-based material loading, are presented. The photocatalytic CO2 reduction mechanism and pathways of TiO2 are discussed. The future research direction and perspective of photocatalytic CO2 reduction over surface-modified TiO2 are also presented.

  17. Enhanced removal of nitrate from water using surface modification of adsorbents--a review.

    Science.gov (United States)

    Loganathan, Paripurnanda; Vigneswaran, Saravanamuthu; Kandasamy, Jaya

    2013-12-15

    Elevated concentration of nitrate results in eutrophication of natural water bodies affecting the aquatic environment and reduces the quality of drinking water. This in turn causes harm to people's health, especially that of infants and livestock. Adsorbents with the high capacity to selectively adsorb nitrate are required to effectively remove nitrate from water. Surface modifications of adsorbents have been reported to enhance their adsorption of nitrate. The major techniques of surface modification are: protonation, impregnation of metals and metal oxides, grafting of amine groups, organic compounds including surfactant coating of aluminosilicate minerals, and heat treatment. This paper reviews current information on these techniques, compares the enhanced nitrate adsorption capacities achieved by the modifications, and the mechanisms of adsorption, and presents advantages and drawbacks of the techniques. Most studies on this subject have been conducted in batch experiments. These studies need to include continuous mode column trials which have more relevance to real operating systems and pilot-plant trials. Reusability of adsorbents is important for economic reasons and practical treatment applications. However, only limited information is available on the regeneration of surface modified adsorbents.

  18. Effect of surface modification of metal hydride electrode on performance of MH/Ni batteries

    Institute of Scientific and Technical Information of China (English)

    YANG Kai; WU Feng; CHEN Shi; ZHANG Cun-zhong

    2007-01-01

    A novel method was applied to the surface modification of the metal hydride(MH) electrode of MH/Ni batteries. Both sides of the electrode were plated with a thin silver film about 0.1μm thick using vacuum evaporation plating technology, and the effect of the electrode on the performance of MH/Ni batteries was examined. It is found that the surface modification can enhance the electrode conductivity and decrease the battery ohimic resistance. After surface modification, the discharge capacity at 5C (7.5A) is increased by 212 mA·h and the discharge voltage is increased by 0.11 V, the resistance of the batteries is also decreased by 32%. The batteries with modified electrode exhibit satisfactory durability. The remaining capacity of the modified batteries is 89% of the initial capacity even after 500 cycles. The inner pressure of the batteries during overcharging is lowered and the charging efficiency of the batteries is improved.

  19. Critical overview of Nitinol surfaces and their modifications for medical applications.

    Science.gov (United States)

    Shabalovskaya, S; Anderegg, J; Van Humbeeck, J

    2008-05-01

    Nitinol, a group of nearly equiatomic shape memory and superelastic NiTi alloys, is being extensively explored for medical applications. Release of Ni in the human body, a potential problem with Nitinol implant devices, has stimulated a great deal of research on its surface modifications and coatings. In order to use any of the developed surfaces in implant designs, it is important to understand whether they really have advantages over bare Nitinol. This paper overviews the current situation, discusses the advantages and disadvantages of new surfaces as well as the limitations of the studies performed. It presents a comprehensive analysis of surface topography, chemistry, corrosion behavior, nickel release and biological responses to Nitinol surfaces modified mechanically or using such methods as etching in acids and alkaline solutions, electropolishing, heat and ion beam treatments, boiling in water and autoclaving, conventional and ion plasma implantations, laser melting and bioactive coating deposition. The analysis demonstrates that the presently developed surfaces vary in thickness from a few nanometers to micrometers, and that they can effectively prevent Ni release if the surface integrity is maintained under strain and if no Ni-enriched sub-layers are present. Whether it is appropriate to use various low temperature pre-treatment protocols (< or = 160 degrees C) developed originally for pure titanium for Nitinol surface modifications and coatings is also discussed. The importance of selection of original Nitinol surfaces with regard to the performance of coatings and comparative performance of controls in the studies is emphasized. Considering the obvious advantages of bare Nitinol surfaces for superelastic implants, details of their preparation are also outlined.

  20. Surface modifications on InAs decrease indium and arsenic leaching under physiological conditions

    Science.gov (United States)

    Jewett, Scott A.; Yoder, Jeffrey A.; Ivanisevic, Albena

    2012-11-01

    Devices containing III-V semiconductors such as InAs are increasingly being used in the electronic industry for a variety of optoelectronic applications. Furthermore, the attractive chemical, material, electronic properties make such materials appealing for use in devices designed for biological applications, such as biosensors. However, in biological applications the leaching of toxic materials from these devices could cause harm to cells or tissue. Additionally, after disposal, toxic inorganic materials can leach from devices and buildup in the environment, causing long-term ecological harm. Therefore, the toxicity of these materials along with their stability in physiological conditions are important factors to consider. Surface modifications are one common method of stabilizing semiconductor materials in order to chemically and electronically passivate them. Such surface modifications could also prevent the leaching of toxic materials by preventing the regrowth of the unstable surface oxide layer and by creating an effective barrier between the semiconductor surface and the surrounding environment. In this study, various surface modifications on InAs are developed with the goal of decreasing the leaching of indium and arsenic. The leaching of indium and arsenic from modified substrates was assessed in physiological conditions using inductively coupled plasma mass spectrometry (ICP-MS). Substrates modified with 11-mercapto-1-undecanol (MU) and graft polymerized with poly(ethylene) glycol (PEG) were most effective at preventing indium and arsenic leaching. These surfaces were characterized using contact angle analysis, ellipsometry, atomic force microscopy (AFM), and X-ray photoelectron spectroscopy (XPS). Substrates modified with collagen and synthetic polyelectrolytes were least effective, due to the destructive nature of acidic environments on InAs. The toxicity of modified and unmodified InAs, along with raw indium, arsenic, and PEG components was assessed

  1. β-Cristobalite (001) surface as 4-formaminoantipyrine adsorbent: First principle study of the effect on adsorption of surface modification.

    Science.gov (United States)

    Simonetti, S; Compañy, A Díaz; Brizuela, G; Juan, A

    2016-12-01

    Silica based materials find applications as excipients and particularly as drug delivery agents for pharmaceutical drugs. Their performance can be crucially affected by surface treatments, as it can modify the adsorption (and release) of these formulations. The role of surface modification on the features of 4-formaminoantipyrine (FAA) adsorbed on β-cristobalite (001) surface is studied by means of simulations based on the Density Functional Theory (DFT). Starting from the results of FAA in interaction with a dehydroxylated surface; a fully hydroxylated surface and a functionalized surface with benzalkonium chloride (BC) surfactant have been added to study the configurational landscape. Calculations suggest that the trend for FAA preferential adsorption on silica surfaces is: dehydroxylated>hydroxylated>BC-functionalized. The potential for hydrogen bonding causes the main contribution to the bonding while dispersion forces present an additional contribution independently of whether the drug is hydrogen-bonded or BC-bonded to the surface. Adsorption takes mainly place through nitrogen atoms in the heterocyclic ring, the carbonyl and amine functional groups. Associated mode's shifts and concurrent changes in bond length are also observed showing accordance between electronic and geometrical structure results. BC surfactant reduces the number of formed H-bonds and lowers the attractive molecule-surface interaction being it useful to prevent particle agglomeration and could favor drug release in therapies that requires faster but controlled delivery.

  2. A short review on Ferrofluids surface modification by natural and biocompatible polymers

    Directory of Open Access Journals (Sweden)

    Mahyar Ebrahimi

    2016-07-01

    Full Text Available This paper provides an overview of how the surface properties of ferromagnetic nanoparticles dispersed in fluids is modified by natural and biocompatible polymers. Among common magnetic nanoparticles, magnetite (Fe3O4 and maghemite (g-Fe203 are popular candidates because of their biocompatibility. Natural polymeric coating materials are the most commonly used biocompatible magnetic nanoparticle coatings. In this paper, recent progresses in the methods of ferrofluids surface modification by the common natural polymers consisting of dextran, chitosan, gelatin and starch are reviewed.

  3. Modification of cell surface properties of Pseudomonas alcaligenes S22 during hydrocarbon biodegradation.

    Science.gov (United States)

    Kaczorek, Ewa; Moszyńska, Sylwia; Olszanowski, Andrzej

    2011-04-01

    Biodegradation of water insoluble hydrocarbons can be significantly increased by the addition of natural surfactants one. Very promising option is the use of saponins. The obtained results indicated that in this system, after 21 days, 92% biodegradation of diesel oil could be achieved using Pseudomonas alcaligenes. No positive effect on the biodegradation process was observed using synthetic surfactant Triton X-100. The kind of carbon source influences the cell surface properties of microorganisms. Modification of the surface cell could be observed by control of the sedimentation profile. This analytical method is a new approach in microbiological analysis.

  4. A General Procedure for Surface Modification of Nano-alumina and Its Application to Dendrimers

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A general procedure for surface modification of nano-alumina using N, N'-dicyclohexyl-carbodiimide (DCC) mediated amidation is reported. Aliphatic and aromatic carboxylic acids reacted smoothly with nano-alumina pretreated with 3-aminopropyltriethoxysilane in the presence of DCC, giving modified aluminas having organic surfaces. The grafted aluminas have been characterized qualitatively by FT-IR or 13C CPMAS NMR spectroscopy, and quantitatively by thermogravimetric analysis and elemental analysis. The procedure was applied to polyether dendrons bearing carboxyl groups at the focal points, giving successful grafting of dendrimers onto nano-alumina.

  5. [Surface modification and microstructure of single-walled carbon nanotubes for dental composite resin].

    Science.gov (United States)

    Xia, Yang; Zhang, Feimin; Xu, Li'na; Gu, Ning

    2006-12-01

    In order to improve its dispersion condition in dental composite resin and enhance its interaction with the matrix, single-walled carbon nanotubes(SWNTs) were refluxed and oxidized, then treated by APTE. Their outer surface were coated by nano-SiO2 particles using sol-gel process, then further treated by organosilanes ATES. IR and TEM were used to analyze modification results. TEM pictures showed nano-particles were on the surface of SWNTs; IR showed characteristic adsorbing bands of SiO2. Composite resin specimen with modified SWNTs was prepared and examined by TEM. SWNTs were detected in composite resin matrix among other inorganic fillers.

  6. QUANTUM-CHEMICAL MODIFICATIONS OF SURFACE:NEW METHODS FOR PROTECTING MATERIALS FROM CORROSION

    Institute of Scientific and Technical Information of China (English)

    R. T. Malkhasyan

    2001-01-01

    A new method of corrosion-resistant coating of technical iron is presented. Processingby vibrationally excited hydrogen molecules of the iron surface covered with oxide filmof a-Fe2O3 results in modification of surface by creating a film of amorphous ironon it. The presence of iron films with crystalline and amorphous phases, having thedifferent Fermi levels, leads tO formation of potential differences between them. Thispotential difference is opposite to the external electric field, resulting in decrease ofanode current and increase of corrosion resistance.

  7. Surface hydrophobic modification of cellulose membranes by plasma-assisted deposition of hydrocarbon films

    Directory of Open Access Journals (Sweden)

    Mudtorlep Nisoa

    2010-03-01

    Full Text Available Surface modification by plasma polymerization is an efficient method to change the surface properties of a membrane. Desirable functionality such as hydrophobicity or hydrophilicity can be obtained, depending on plasma chemistry of gas precursors and discharge conditions. In this work, RF magnetron plasma is produced using acetylene and nitrogen as precursor gases. Variations of RF power, particle flux, deposited time and pressure of the precursor gases have been made to observe coating effects on the cellulose membranes. When appropriated conditions are used, a thin brownish film of hydrocarbon was formed on the membrane, and the water contact angle increased from 35 to 130 degrees.

  8. Effect of Surface Modification on Microwave Absorbing Properties of Magnetic Metal Fibers

    Institute of Scientific and Technical Information of China (English)

    XIE Wei; CHENG Haifeng; CHU Zengyong; ZHOU Yongjiang; TANG Gengping; XU Yongping

    2007-01-01

    In order to avoid forming an electrical conductive network due to surface connections, the magnetic metal fibers were coated with SiO2 for surface modification by the sol-gel process. The microstructure, composition and electromagnetic characteristics of SiO2 -coated and uncoated metal fibers were studied using SEM, EDAX, and a voter network analyzer. The reflectivity was simulated using the RAMCAD software. The electromagnetic parameters and absorption properties of SiO2-coated metal fibers were improved greatly due to optimal impendence matching and the electric conductivity decreased, compared to those of uncoated materials.

  9. Bioactive surface modification on amide-photografted poly(3-hydroxybutyrate-co-3-hydroxyvalerate)

    Energy Technology Data Exchange (ETDEWEB)

    Ke Yu; Xue Wei [Institute of Life and Health Engineering, Jinan University, Guangzhou (China); Wang Yingjun; Ren Li; Wu Gang, E-mail: lisa6863@163.com [Biomaterial Research Institute, College of Material Science and Engineering, South China University of Technology, Guangzhou (China)

    2011-04-15

    Collagen was chemically immobilized on poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) films via hydrophilic polyacrylamide spacers, aiming to establish the bioactive surface and the inner surface models. The inner surface modified films presented higher wettability than the surface modified films. Wide-angle x-ray diffraction results showed that the d-spacing values of the inner surface model increased compared with those of the surface model, but there was no significant difference between the amide- and collagen-modified PHBV films. The peak melting temperatures of PHBV and the special endotherm around 70 {sup 0}C were following the order: PHBV > amide-modified PHBV > collagen-modified PHBV. The weight loss of the collagen-modified PHBV (inner surface model) might involve hydrolyzation and mineralization during 360 days of incubation, with a maximum value of 18.24%, while PHBV films did not show significant weight loss. The pH value of the degradation fluids fluctuated in the range of 6.86-7.22, as the initial pH was recorded at 7.20. Based on the surface model, collagen-modified PHBV scaffolds were prepared, which enhanced chondrocyte adhesion and spread on the biomimetic surface. Two surface modification models might develop a protocol with a view to generating a biocompatible and biomechanical scaffold for use in meniscus regeneration.

  10. Controlled modification of the structure of polymer surfaces by chemically grafting inorganic species

    Directory of Open Access Journals (Sweden)

    Rodrigo Lambert Oréfice

    1999-07-01

    Full Text Available Many chemical and physical methods, such as plasma, e-beam, sputtering, CVD and others, have been used to modify the structure of polymer surfaces by depositing thin inorganic films. Most of these techniques are based upon the use of high energy sources that ultimately can damage either chemically or physically polymer surfaces. Moreover, these methods are usually not versatile enough to allow the design of structurally and chemically tailored surfaces through the control of the distribution of chemical functionalities throughout the surface. In this work, inorganic species were introduced onto polymer substrates in a controlled manner by performing a sequence of chemical reactions at the surface. Sulfonation followed by silanization reactions were used to graft alkoxysilane species at the surface of poly(aryl sulfones. The heterogeneous chemical modification of poly(aryl sulfones was monitored by FTIR-ATR (Attenuated Total Reflection - FTIR. Model compounds were used to study the chemical reactions occurring during the grafting procedure. The results showed that the developed procedure can allow a controlled introduction of inorganic species onto polymer surfaces. Furthermore, in order to prove that this procedure enables the deposition of specific chemical functionalities onto polymer surfaces that can be used to create chemically and structurally tailored surfaces, silicate films were deposited on previously silanated PAS bioactive glass composites. In vitro tests showed that the surface modified composite can enhance the rates of hydroxy-carbonate-apatite precipitation.

  11. Interaction of Gram-negative bacteria with cationic proteins: Dependence on the surface characteristics of the bacterial cell

    Directory of Open Access Journals (Sweden)

    Isabella R Prokhorenko

    2009-03-01

    Full Text Available Isabella R Prokhorenko1, Svetlana V Zubova1, Alexandr Yu Ivanov2, Sergey V Grachev31Laboratory of Molecular Biomedicine, Institute of Basic Biological Problems; 2Institute of Cell Biophysics, Russian Academy of Sciences, Moscow, Russia; 3I.M. Sechenov’s Moscow Medical Academy, Moscow, Russia Abstract: Gram-negative bacteria can enter the bloodstream and interact with serum cationic proteins. The character of interaction will depend on the surface characteristics of bacterial cells, which are determined by bacterial chemotype and density of lipopolysaccharide (LPS packing in the cell wall. It was shown that the lysozyme treatment resulted in the increase sensitivity to hypotonic shock. Signifi cant differences to this effect were found between Escherichia coli strain D21 and D21f2 under treatment with physiological protein concentration. On the basis of electrokinetic measurements and studies of the interaction of cells with lysozyme, the hypothesis was formed that the cell wall of the E. coli strain D21f2 contains more LPS and has a higher density of their packing than the cell wall of the E. coli D21 cells. The effect of lysozyme and lactoferrin on the viability of E. coli cells of two different strains was examined. Lysozyme was found to more effectively inhibit the growth of the E. coli D21 bacteria, and lactoferrin suppressed mainly the growth of the E. coli D21f2 bacteria. These results indicate that the differences in LPS core structure of bacterial R-chemotype, which determines surface charge and density of LPS packing, plays an essential role in the mechanisms of interaction of the cationic proteins with the cell wall.Keywords: lipopolysaccharide, Escherichia coli, chemotype, lysozyme, lactoferrin, colony-forming units

  12. Creation of hydrophilic nitric oxide releasing polymers via plasma surface modification.

    Science.gov (United States)

    Pegalajar-Jurado, A; Joslin, J M; Hawker, M J; Reynolds, M M; Fisher, E R

    2014-08-13

    Herein, we describe the surface modification of an S-nitrosated polymer derivative via H2O plasma treatment, resulting in polymer coatings that maintained their nitric oxide (NO) releasing capabilities, but exhibited dramatic changes in surface wettability. The poly(lactic-co-glycolic acid)-based hydrophobic polymer was nitrosated to achieve a material capable of releasing the therapeutic agent NO. The NO-loaded films were subjected to low-temperature H2O plasma treatments, where the treatment power (20-50 W) and time (1-5 min) were varied. The plasma treated polymer films were superhydrophilic (water droplet spread completely in plasma-treated materials; however, they still result in physiologically relevant NO fluxes. XPS, SEM-EDS, and ATR-IR characterization suggests the plasma treatment resulted in polymer rearrangement and implantation of hydroxyl and carbonyl functional groups. Plasma treated samples maintained both hydrophilic surface properties and NO release profiles after storage at -18 °C for at least 10 days, demonstrating the surface modification and NO release capabilities are stable over time. The ability to tune polymer surface properties while maintaining bulk properties and NO release properties, and the stability of those properties under refrigerated conditions, represents a unique approach toward creating enhanced therapeutic biopolymers.

  13. Laser surface modification of ultra-high-molecular-weight polyethylene (UHMWPE) for biomedical applications

    Energy Technology Data Exchange (ETDEWEB)

    Riveiro, A., E-mail: ariveiro@uvigo.es [Applied Physics Department, University of Vigo, ETSII, Lagoas-Marcosende, 9, Vigo 36310 (Spain); Centro Universitario de la Defensa, Escuela Naval Militar, Plaza de España 2, 36920 Marín (Spain); Soto, R.; Val, J. del; Comesaña, R.; Boutinguiza, M.; Quintero, F.; Lusquiños, F.; Pou, J. [Applied Physics Department, University of Vigo, ETSII, Lagoas-Marcosende, 9, Vigo 36310 (Spain)

    2014-05-01

    Ultra-high-molecular-weight polyethylene (UHMWPE) is a synthetic polymer used for biomedical applications because of its high impact resistance, ductility and stability in contact with physiological fluids. Therefore, this material is being used in human orthopedic implants such as total hip or knee replacements. Surface modification of this material relates to changes on its chemistry, microstructure, roughness, and topography, all influencing its biological response. Surface treatment of UHMWPE is very difficult due to its high melt viscosity. This work presents a systematic approach to discern the role of different laser wavelengths (λ = 1064, 532, and 355 nm) on the surface modification of carbon coated UHMWPE samples. Influence of laser processing conditions (irradiance, pulse frequency, scanning speed, and spot overlapping) on the surface properties of this material was determined using an advanced statistical planning of experiments. A full factorial design of experiments was used to find the main effects of the processing parameters. The obtained results indicate the way to maximize surface properties which largely influence cell–material interaction.

  14. Surface modification of positive electrode materials for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Julien, C.M., E-mail: Christian.Julien@upmc.fr [Sorbonne Universités, UPMC Univ. Paris 6, Physicochimie des Electrolytes et Nanosystèmes Interfaciaux (PHENIX), UMR 8234, 75005 Paris (France); Mauger, A. [Institut de Minéralogie de Physique des Matériaux et de Cosmochimie (IMPMC), UPMC Univ. Paris 6, 4 place Jussieu, 75005 Paris (France); Groult, H. [Sorbonne Universités, UPMC Univ. Paris 6, Physicochimie des Electrolytes et Nanosystèmes Interfaciaux (PHENIX), UMR 8234, 75005 Paris (France); Zaghib, K. [Energy Storage and Conversion, Research Institute of Hydro-Québec, Varennes, Québec J3X 1S1 (Canada)

    2014-12-01

    The advanced lithium-ion batteries are critically important for a wide range of applications, from portable electronics to electric vehicles. The research on their electrodes aims to increase the energy density and the power density, improve the calendar and the cycling life, without sacrificing the safety issues. A constant progress through the years has been obtained owing to the surface treatment of the particles, in particular the coating of the nanoparticles with a layer that protects the core region from side reactions with the electrolyte, prevents the loss of oxygen, and the dissolution of the metal ions in the electrolyte, or simply improve the conductivity of the powder. The purpose of the present work is to present the different surface modifications that have been tried for three families of positive electrodes: layered, spinel and olivine frameworks that are currently considered as promising materials. The role of the different coats used to improve either the surface conductivity, or the thermal stability, or the structural integrity is discussed. - Highlights: • Report the various surface modifications tried for the positive electrodes of Li-ion batteries. • The role of different coats used to improve the conductivity, or the thermal stability, or the structural integrity. • Improvement of electrochemical properties of electrodes after coating or surface treatment.

  15. Surface modification of polycaprolactone scaffolds fabricated via selective laser sintering for cartilage tissue engineering

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Chih-Hao [Department of Chemical and Materials Engineering, Chang Gung University, Kweishan, Taoyuan 333, Taiwan, ROC (China); Department of Plastic and Reconstructive Surgery, Chang Gung Memorial Hospital, Craniofacial Research Center, Chang Gung University, Kweishann, Taoyuan 333, Taiwan, ROC (China); Lee, Ming-Yih [Graduate Institute of Medical Mechatronics, Chang Gung University, Kweishan, Taoyuan 333, Taiwan, ROC (China); Shyu, Victor Bong-Hang; Chen, Yi-Chieh; Chen, Chien-Tzung [Department of Plastic and Reconstructive Surgery, Chang Gung Memorial Hospital, Craniofacial Research Center, Chang Gung University, Kweishann, Taoyuan 333, Taiwan, ROC (China); Chen, Jyh-Ping, E-mail: jpchen@mail.cgu.edu.tw [Department of Chemical and Materials Engineering, Chang Gung University, Kweishan, Taoyuan 333, Taiwan, ROC (China); Research Center for Industry of Human Ecology, Chang Gung University of Science and Technology, Kweishan, Taoyuan 333, Taiwan, ROC (China)

    2014-07-01

    Surface modified porous polycaprolactone scaffolds fabricated via rapid prototyping techniques were evaluated for cartilage tissue engineering purposes. Polycaprolactone scaffolds manufactured by selective laser sintering (SLS) were surface modified through immersion coating with either gelatin or collagen. Three groups of scaffolds were created and compared for both mechanical and biological properties. Surface modification with collagen or gelatin improved the hydrophilicity, water uptake and mechanical strength of the pristine scaffold. From microscopic observations and biochemical analysis, collagen-modified scaffold was the best for cartilage tissue engineering in terms of cell proliferation and extracellular matrix production. Chondrocytes/collagen-modified scaffold constructs were implanted subdermally in the dorsal spaces of female nude mice. Histological and immunohistochemical staining of the retrieved implants after 8 weeks revealed enhanced cartilage tissue formation. We conclude that collagen surface modification through immersion coating on SLS-manufactured scaffolds is a feasible scaffold for cartilage tissue engineering in craniofacial reconstruction. - Highlights: • Selective laser sintered polycaprolactone scaffolds are prepared. • Scaffolds are surface modified through immersion coating with gelatin or collagen. • Collagen-scaffold is the best for cartilage tissue engineering in vitro. • Chondrocytes/collagen-scaffold reveals enhanced cartilage tissue formation in vivo.

  16. Inward Cationic Diffusion and Formation of Silica-Rich Surface Nanolayer of Glass

    DEFF Research Database (Denmark)

    Smedskjær, Morten Mattrup; Deubener, Joachim; Yue, Yuanzheng

    2009-01-01

    This paper reports a chemical approach for obtaining a silica-rich nanolayer on the surface of a vanadium-bearing silicate glass. The approach involves depletion of earth alkaline ions (Mg2+ and Ca2+) from the glass surface by means of inward diffusion of those ions, i.e., diffusion from the surf......This paper reports a chemical approach for obtaining a silica-rich nanolayer on the surface of a vanadium-bearing silicate glass. The approach involves depletion of earth alkaline ions (Mg2+ and Ca2+) from the glass surface by means of inward diffusion of those ions, i.e., diffusion from...... form and are incorporated into the glass structure. Both the V4+ and the hydroxyl contents increase with increasing ta and hydrogen partial pressure. The inward diffusion enhances the hardness of the glass surface. The mechanism of the inward diffusion is suggested on the basis of a model describing...... the outward diffusion. The new approach provides a possibility to create a silica-rich nanolayer on glass surfaces by means of the inward diffusion process....

  17. Effects of Ultrasonic Nanocrystal Surface Modification (UNSM) on Residual Stress State and Fatigue Strength of AISI 304

    Science.gov (United States)

    Cherif, A.; Pyoun, Y.; Scholtes, B.

    2010-03-01

    The effects of a new mechanical surface treatment method, called ultrasonic nanocrystal surface modification (UNSM), on near-surface microstructures and residual stress states as well as on the fatigue behavior of an austenitic steel AISI 304 are investigated and discussed. The results are compared with consequences of other mechanical surface treatment methods such as deep rolling or shot peening.

  18. Surface Modification of α-Fe Metal Particles by Chemical Surface Coating

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The structure of α-Fe metal magnetic recording particles coated with silane coupling agents have been studied by TEM, FT-IR, EXAFS, Mossbauer. The results show that a close, uniform, firm and ultra thin layer, which is beneficial to the magnetic and chemical stability, has been formed by the cross-linked chemical bond Si-O-Si. And the organic molecule has chemically bonded to the particle surface, which has greatly affected the surface Fe atom electronic structure. Furthermore, the covalent bond between metal particle surface and organic molecule has obvious effect on the near edge structure of the surface Fe atoms.

  19. Surface modification of bioactive glasses and preparation of PDLLA/bioactive glass composite films.

    Science.gov (United States)

    Gao, Yuan; Chang, Jiang

    2009-08-01

    In order to improve the homogeneous dispersion of particles in the polymeric matrix, 45S5, mesoporous 58S, and 58S bioactive glasses were surface modified by esterification reactions with dodecyl alcohol at reflux temperature of 260 degrees C (named as m-45S5, m-mesoporous 58S, and m-58S, respectively). The modified particles showed better hydrophobicity and longer time of suspension in organic matrix. The PDLLA/bioactive glass composite films were fabricated using surface modified bioactive glass particles through solvent casting-evaporation method. Surface morphology, mechanical property, and bioactivity were investigated. The results revealed that the inorganic particle distribution and tensile strength of the composite films with modified bioactive glass particles were significantly improved while great bioactive properties were maintained. Scanning electron microscopy (SEM) observation illustrated that the modified bioactive glass particles were homogeneously dispersed in the PDLLA matrix. The maximum tensile strengths of composite films with modified bioactive glass particles were higher than that of composite films with unmodified bioactive glass particles. The bioactivity of the composite films were evaluated by being soaked in the simulated body fluid (SBF) and the SEM observation of the films suggested that the modified composite films were still bioactive in that they could induce the formation of HAp on its surface and the distribution of HAp was even more homogeneous on the film. The results mentioned above indicated that the surface modification of bioactive glasses with dodecyl alcohol was an effective method to prepare PDLLA/bioactive glass composites with enhanced properties. By studying the comparisons of modification effects among the three types of bioactive glasses, we could get the conclusion that the size and morphology of the inorganic particles would greatly affect the modification effects and the properties of composites.

  20. Surface modification with both phosphorylcholine and stearyl groups to adjust hydrophilicity and hydrophobicity

    Energy Technology Data Exchange (ETDEWEB)

    Lv Jiuan; Ma Jiani; Huangfu Pengbo; Yang Shan [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, Department of Chemistry, Northwest University, Xi' an 710069 (China); Gong Yongkuan [Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, Department of Chemistry, Northwest University, Xi' an 710069 (China)], E-mail: gongyk@nwu.edu.cn

    2008-11-15

    A new monolayer film with tunable hydrophilicity and hydrophobicity was constructed on glass coverslips by stepwise grafting with both phosphorylcholine (PC) and stearyl groups. The glass coverslips were firstly hydroxylized to provide reactive sites on the surfaces. Subsequently, chlorodimethyl-n-octadecylsilane was chemically adsorbed onto the surface to impart the required hydrophobicity. The remaining hydroxyl groups were grafted with 1,6-diisocyanatohexane. Finally, 2-hydroxy-2-ethylphosphorylcholine was grafted onto the attached isocyanate groups. Dynamic contact angle (DCA) measurement and X-ray photoelectron spectroscopy (XPS) analysis confirmed that the step-by-step modification process was successful. The adsorption of bovine serum albumin and bovine plasma fibrinogen, as well as the adhesion and aggregation of platelets were suppressed with the introduction of phospholipid moieties on the surfaces. This tunable surface may have potential applications in the fields of separation science, tissue engineering, cytobiology, drug delivery and gene therapy.

  1. Surface modification of polytetrafluoroethylene film using single liquid electrode atmosphericpressure glow discharge

    Institute of Scientific and Technical Information of China (English)

    Zhou Lan; Lü Guo-Hua; Chen Wei; Pang Hua; Zhang Gu-Ling; Yang Si-Ze

    2011-01-01

    Polytetrafluoroethylene films are treated by room temperature helium atmospheric pressure plasma plumes, which are generated with a home-made single liquid electrode plasma device. After plasma treatment, the water contact angle of polytetrafluoroethylene film drops from 114° to 46° and the surface free energy increases from 22.0 mJ/m2 to 59.1 mJ/m2. The optical emission spectrum indicates that there are reactive species such as O2+, O and He in the plasma plume. After plasma treatment, a highly crosslinking structure is formed on the film surface and the oxygen element is incorporated into the film surface in the forms of -C-O-C-, -C=O, and -O-C=O groups. Over a period of 10 days, the contact angle of the treated film is recovered by only about 10°, which indicates that the plasma surface modification is stable with time.

  2. Surface Modification of Polyethylene (PE) Films Using Dielectric Barrier Discharge Plasma at Atmospheric Pressure

    Institute of Scientific and Technical Information of China (English)

    WANG Kun; LI Jian; REN Chunsheng; WANG Dezhen; WANG Younian

    2008-01-01

    Modification of the surface properties of polyethylene (PE) films is studied using air dielectric barrier discharge at atmospheric pressure. The treated samples are examined by water contact angle measurements, Fourier transform infrared attenuated total reflection spectroscopy (FTIR-ATR), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). With the increase in treating time, the water contact angle changes from 93.2° before treatment to a minimum of 53.3° after a treatment for 50 s. Both ATR and XPS results show some oxidized" species are introduced into the sample surface by the plasma treatment and the tendency of the water contact angle with the treating time is the same as that of oxygen concentration on the treated sample surface. SEM result shows the surface roughness of PE samples increases with the treatment time increasing.

  3. Surface modifications of W divertor components for EAST during exposure to high heat loads with He

    Energy Technology Data Exchange (ETDEWEB)

    Li, C., E-mail: lichun10@mails.tsinghua.edu.cn [Laboratory of Advanced Materials, School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Greuner, H. [Max Planck Institute for Plasma Physics, Boltzmannstr. 2, 85748 Garching (Germany); Yuan, Y. [School of Physics and Nuclear Energy Engineering, Beihang University, Beijing 100191 (China); Zhao, S.X.; Luo, G.N. [Institute of Plasma Physics, Chinese Academy of Sciences, Hefei, Anhui 230031 (China); Böswirth, B. [Max Planck Institute for Plasma Physics, Boltzmannstr. 2, 85748 Garching (Germany); Fu, B.Q.; Jia, Y.Z. [Laboratory of Advanced Materials, School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China); Liu, X. [Southwestern Institute of Physics, Chengdu, Sichuan 610041 (China); Liu, W., E-mail: liuw@mail.tsinghua.edu.cn [Laboratory of Advanced Materials, School of Materials Science and Engineering, Tsinghua University, Beijing 100084 (China)

    2015-08-15

    Flat-type W/Cu plasma-facing components have been developed for the new generation divertor of the Chinese Experimental Advanced Superconducting Tokamak. Surface modifications of such actively water-cooled W components following short and long pulse high heat loading coupled with He particle loads with fluence of 3 × 10{sup 22} m{sup −2} have been investigated. An adiabatically loaded W block was investigated as a comparison and exposed to short pulse loads. Blistering was observed on all sample surfaces, but was less pronounced on the components than on the W block, due to the significant lower surface temperature caused by active cooling. For components, longer pulse loads gave rise to a rougher surface. Furthermore, most blisters on components are found to be less than 1 μm in diameter, with just a very few blisters larger than 1 μm, observed only in some near 〈1 1 1〉 grains.

  4. Chemical modification of TiO2 surfaces with methylsilanes and characterization by infrared absorption spectroscopy

    Science.gov (United States)

    Finklea, H. O.; Vithanage, R.

    1982-01-01

    Infrared absorption spectra of methylsilanes bonded to a TiO2 powder were obtained. The reacting silanes include Me sub (4-n)SiX sub n (n=1-4; X=Cl, OMe) and hexamethyldisilazane (HMDS). Reactions were performed on hydroxylated-but-anhydrous TiO2 surfaces in the gas phase. IR spectra confirm the presence of a bonded silane layer. Terminal surface OH groups are found to react more readily than bridging OH groups. By-products of the modification adsorp tenaciously to the surface. The various silanes show only small differences in their ability to sequester surface OH groups. Following hydrolysis in moist air, Si-OH groups are observed only for the tetrafunctional silanes.

  5. Extreme ultraviolet (EUV) surface modification of polytetrafluoroethylene (PTFE) for control of biocompatibility

    Energy Technology Data Exchange (ETDEWEB)

    Ahad, Inam Ul, E-mail: inam-ul.ahad@wat.edu.pl [Institute of Optoelectronics, Military University of Technology, 00-908 Warsaw (Poland); Advanced Processing Technology Research Centre, School of Mechanical and Manufacturing Engineering, Faculty of Engineering & Computing, Dublin City University, Dublin 9 (Ireland); Butruk, Beata [Department of Biotechnology and Bioprocess Engineering, Warsaw University of Technology, Ul. Waryńskiego 1, 00-645 Warsaw (Poland); Ayele, Mesfin; Budner, Bogusław; Bartnik, Andrzej; Fiedorowicz, Henryk [Institute of Optoelectronics, Military University of Technology, 00-908 Warsaw (Poland); Ciach, Tomasz [Department of Biotechnology and Bioprocess Engineering, Warsaw University of Technology, Ul. Waryńskiego 1, 00-645 Warsaw (Poland); Brabazon, Dermot [Advanced Processing Technology Research Centre, School of Mechanical and Manufacturing Engineering, Faculty of Engineering & Computing, Dublin City University, Dublin 9 (Ireland)

    2015-12-01

    Extreme ultraviolet (EUV) surface modification of polytetrafluoroethylene (PTFE) was performed in order to enhance the degree of biocompatibility. Polymer samples were irradiated by different number of EUV shots using a laser–plasma based EUV source in the presence of nitrogen gas. The physical and chemical properties of EUV modified PTFE samples were studied using Atomic Force Microscopy, X-ray photoelectron spectroscopy and water contact angle (WCA) methods. Pronounced wall type micro and nano-structures appeared on the EUV treated polymer surfaces resulting in increased surface roughness and hydrophobicity. Stronger cell adhesion and good cell morphology were observed on EUV modified surfaces by in-vitro cell culture studies performed using L929 fibroblasts.

  6. Comparison of two different plasma surface-modification techniques for the covalent immobilization of protein monolayers.

    Science.gov (United States)

    Cifuentes, Anna; Borrós, Salvador

    2013-06-04

    The immobilization of biologically active species is crucial for the fabrication of smart bioactive surfaces. For this purpose, plasma polymerization is frequently used to modify the surface nature without affecting the bulk properties of the material. Thus, it is possible to create materials with surface functional groups that can promote the anchoring of all kinds of biomolecules. Different methodologies in protein immobilization have been developed in recent years, although some drawbacks are still not solved, such as the difficulties that some procedures involve and/or the denaturalization of the protein due to the immobilization process. In this work, two different strategies to covalently attach bovine serum albumin (BSA) protein are developed. Both techniques are compared in order to understand how the nature of the surface modification affects the conformation of the protein upon immobilization.

  7. Hydrophobic surface modification of chitosan gels by stearyl for improving the activity of immobilized lipase

    Institute of Scientific and Technical Information of China (English)

    Hong Tao Deng; Juan Juan Wang; Miao Ma; Zhong Yang Liu; Fei Zheng

    2009-01-01

    The hydrophobic surface modification of chitosan gels was carded out using the amidating reaction of amido groups on a gel surface with steafic acid activated by 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (EDC) and N-hydroxy-succinimide (NHS). Lipases from Candida rugosa were adsorbed on the nascent chitosan gels (CS) and stearyl-modified gels (SCS) with different degrees of amidation. The increased surface hydrophobicity of chitosan gels improved the adsorption capacity and activity of the immobilized lipase. SCS with 31.46% amidation showed the maximum activity retention (83.43%). The experimental results suggest that the moderate surface hydrophilicity/hydropbobicity of chitosan gels is necessary for the improvement of the activity of immobilized lipase.

  8. Characterization of surface modification in atomic force microscope-induced nanolithography of oxygen deficient La0.67Ba0.33MnO3−δ thin films

    Directory of Open Access Journals (Sweden)

    E. Kevin Tanyi

    2014-12-01

    Full Text Available We report our studies of the nanolithographic surface modifications induced by an Atomic Force Microscope (AFM in epitaxial thin films of oxygen deficient Lanthanum Barium Manganese Oxide (La0.67Ba0.33MnO3−δ. The pattern characteristics depend on the tip voltage, tip polarity, voltage duration, tip force, and humidity. We have used Electron Energy Dispersive X-Ray Spectroscopy (EDS to analyze the chemical changes associated with the surface modifications produced with a negatively biased AFM tip. A significant increase in the oxygen stoichiometry for the patterned regions relative to the pristine film surface is observed. The results also indicate changes in the cation stoichiometry, specifically a decrease in the Lanthanum and Manganese concentrations and an increase in the Barium concentration in the patterned regions.

  9. Spatially selective modification of PLLA surface: From hydrophobic to hydrophilic or to repellent

    Science.gov (United States)

    Bastekova, Kristina; Guselnikova, Olga; Postnikov, Pavel; Elashnikov, Roman; Kunes, Martin; Kolska, Zdenka; Švorčík, Vaclav; Lyutakov, Oleksiy

    2017-03-01

    A universal approach to controlled surface modification of polylactic acid (PLLA) films using diazonium chemistry was proposed. The multistep procedure includes surface activation of PLLA by argon plasma treatment and chemical activation of arenediazonium tosylates by NaBH4. The surface of PLLA film was grafted with different functional organic groups (OFGs), changing the PLLA surface properties (wettability, morphology, zeta potential, chemical composition, and mechanical response). Three approaches of OFG grafting were examined: (i) plasma treatment following by PLLA immersion into diazonium salt aqueous solution; (ii) grafting of PLLA surface through the reaction with chemically created aryl radicals; (iii) mutual combination of both methods The best results were achieved in the last case, where the previous plasma treatment was combined with further reaction of PLLA surface with generated aryl radicals. Using this method PLLA surface was successfully grafted with amino, carboxyl, aliphatic and fluorinated OFGs. Further investigation of surface properties from potential biological and medical points of view was performed using zeta potential, biodegradation and biofouling tests. It was shown that proposed technique allows preparation of biorepellent or bioabsorptive surfaces, tuning of PLLA biodegradation rate and nanomechanical properties, as well as the introduction of inverse properties (such as hydrophilic and hydrophobic) on both sides of PLLA films.

  10. Chemical modifications of silicon surfaces for the generation of a tunable surface isoelectric point

    NARCIS (Netherlands)

    van der Maaden, Koen; Tomar, Jasmine; Jiskoot, Wim; Bouwstra, Joke

    2014-01-01

    The aim of this work was to generate a tunable surface isoelectric point (sIEP), where the surface is modified with two molecules: a weak base (pyridine), carrying a pH dependent positive charge, and a derivative of a strong acid (sulfate), carrying a permanent negative charge in a physiologically r

  11. Surface modification of nanoporous alumina surfaces with poly(ethylene glycol).

    Science.gov (United States)

    Popat, Ketul C; Mor, Gopal; Grimes, Craig A; Desai, Tejal A

    2004-09-14

    Nanoporous alumina surfaces have a variety of applications in biosensors, biofiltration, and targeted drug delivery. However, the fabrication route to create these nanopores in alumina results in surface defects in the crystal lattice. This results in inherent charge on the porous surface causing biofouling, that is, nonspecific adsorption of biomolecules. Poly(ethylene glycol) (PEG) is known to form biocompatible nonfouling films on silicon surfaces. However, its application to alumina surfaces is very limited and has not been well investigated. In this study, we have covalently attached PEG to nanoporous alumina surfaces to improve their nonfouling properties. A PEG-silane coupling technique was used to modify the surface. Different concentrations of PEG for different immobilization times were used to form PEG films of various grafting densities. X-ray photoelectron spectroscopy (XPS) was used to verify the presence of PEG moieties on the alumina surface. High-resolution C1s spectra show that with an increase in concentration and immobilization time, the grafting density of PEG also increases. Further, a standard overlayer model was used to calculate the thickness of PEG films formed using the XPS intensities of the Al2p peaks. The films formed by this technique are less than 2.5 nm thick, suggesting that such films will not clog the pores which are in the range of 70-80 nm.

  12. Surface modification of droplet polymeric microfluidic devices for the stable and continuous generation of aqueous droplets.

    Science.gov (United States)

    Subramanian, Balamurugan; Kim, Namwon; Lee, Wonbae; Spivak, David A; Nikitopoulos, Dimitris E; McCarley, Robin L; Soper, Steven A

    2011-06-21

    Droplet microfluidics performed in poly(methyl methacrylate) (PMMA) microfluidic devices resulted in significant wall wetting by water droplets formed in a liquid-liquid segmented flow when using a hydrophobic carrier fluid such as perfluorotripropylamine (FC-3283). This wall wetting led to water droplets with nonuniform sizes that were often trapped on the wall surfaces, leading to unstable and poorly controlled liquid-liquid segmented flow. To circumvent this problem, we developed a two-step procedure to hydrophobically modify the surfaces of PMMA and other thermoplastic materials commonly used to make microfluidic devices. The surface-modification route involved the introduction of hydroxyl groups by oxygen plasma treatment of the polymer surface followed by a solution-phase reaction with heptadecafluoro-1,1,2,2-tetrahydrodecyl trichlorosilane dissolved in fluorocarbon solvent FC-3283. This procedure was found to be useful for the modification of PMMA and other thermoplastic surfaces, including polycyclic olefin copolymer (COC) and polycarbonate (PC). Angle-resolved X-ray photoelectron spectroscopy indicated that the fluorination of these polymers took place with high surface selectivity. This procedure was used to modify the surface of a PMMA droplet microfluidic device (DMFD) and was shown to be useful in reducing the wetting problem during the generation of aqueous droplets in a perfluorotripropylamine (FC-3283) carrier fluid and could generate stable segmented flows for hours of operation. In the case of PMMA DMFD, oxygen plasma treatment was carried out after the PMMA cover plate was thermally fusion bonded to the PMMA microfluidic chip. Because the appended chemistry to the channel wall created a hydrophobic surface, it will accommodate the use of other carrier fluids that are hydrophobic as well, such as hexadecane or mineral oils.

  13. Enhanced osteointegration of medical titanium implant with surface modifications in micro/nanoscale structures

    Directory of Open Access Journals (Sweden)

    Liwen Lin

    2014-01-01

    Full Text Available Biomimetic design and substrate-based surface modification of medical implants will help to improve the integration of tissue to its material interfaces. Surface energy, composition, roughness, and topography all influence the biological responses of the implants, such as protein adsorption and cell adhesion, proliferation and differentiation. In the current study, different surface structures of Ti implants were constructed using facile surface techniques to create various micro-, nano-, and nano/micro composite scale topography. We have fabricated three types of hierarchical structures of TiO2 coating on Ti implants, including nanotube structure, nano sponge-like structure, and nano/micro nest-like structure. The osteointegration and biomechanical performance of the coated Ti screws were evaluated by histology and removal of torque force test in vivo. We found that the nano/micro nest-like and nanotube structured surface possessed better osteointegration ability. It indicated that the alkaline hydrothermally treated Ti substrate was the best for bone-implant integration in terms of all in vitro and in vivo testing parameters. The alkaline hydrothermally treated surface displayed a hydrophilic (contact angle value 5.92 ± 1.2, higher roughness (Ra value 911.3 ± 33.8 nm, higher specific surface area (8.26 ± 1.051 m2/g, and greater apatite inductivity. The electrochemical surface modification may become a powerful approach to enhance metal implant to bone integration in orthopaedic applications.

  14. Surface modification of silicon carbide with silane coupling agent and hexadecyl iodiele

    Science.gov (United States)

    Shang, Xujing; Zhu, Yumei; Li, Zhihong

    2017-02-01

    In this paper, two kinds of silane coupling agents, namely 3-aminopropyl triethoxysilane (KH550) and 3-mercaptopropyl trimethoxysilane (KH590), were adopted as preliminary modifiers to improve the hydrophobic surface properties of silicon carbide (SiC) powder for the first step. The factors that influence the modification effects were investigated by measuring the contact angle. The results showed that KH590 has a better effect than KH550 for the hydrophobic modification of SiC, and the contact angle improved most after SiC powder was reacted with 0.3 g KH590 at 75 °C in aqueous/alcohol solution for 4 h. On account of further enhancement of hydrophobicity, the study was focused on utilizing nucleophilic substitution between KH590 and hexadecyl iodiele to extend the length of alkyl chain. Compared with using KH590 alone, SiC powder modified by KH590 and hexadecyl iodiele showed better water resistance with an increase of contact angle from 106.8° to 127.5°. The Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectra (XPS) as well as X-ray diffraction (XRD) analysis results showed that KH550/KH590 and hexadecyl iodiele can be covalently bonded to the surface of SiC powder without altering its crystal configuration. This methodology may provide a new way of the modification of inorganic materials in further.

  15. Surface cellulose modification with 2-aminomethylpyridine for copper, cobalt, nickel and zinc removal from aqueous solution

    Directory of Open Access Journals (Sweden)

    Edson Cavalcanti Silva Filho

    2013-02-01

    Full Text Available Cellulose was first modified with thionyl chloride, followed by reaction with 2-aminomethylpyridine to yield 6-(2'-aminomethylpyridine-6-deoxycellulose. The resulting chemically-immobilized surface was characterized by elemental analysis, FTIR, 13C NMR and thermogravimetry. From 0.28% of nitrogen incorporated in the polysaccharide backbone, the amount of 0.10 ± 0.01 mmol of the proposed molecule was anchored per gram of the chemically modified cellulose. The available basic nitrogen centers attached to the covalent pendant chain bonded to the biopolymer skeleton were investigated for copper, cobalt, nickel and zinc adsorption from aqueous solution at room temperature. The newly synthesized biopolymer gave maximum sorption capacities of 0.100 ± 0.012, 0.093 ± 0.021, 0.074 ± 0.011 and 0.071 ± 0.019 mmol.g-1 for copper, cobalt, nickel and zinc cations, respectively, using the batchwise method, whose data was fitted to different sorption models, the best fit being obtained with the Langmuir model. The results suggested the use of this anchored biopolymer for cation removal from the environment.

  16. Controlled chemical and morphological surface modifications via pulsed plasma polymerizations: Synthesis of ultrahydrophobic surfaces

    Science.gov (United States)

    Qiu, Haibo

    The RF plasma polymerization of saturated linear and cyclic perfluoroalkane monomers and vinyl acetic acid were studied in this dissertation. Film chemical compositions, deposition rates, surface wettabilities and morphologies were characterized as functions of various plasma processing conditions. Large progressive changes in chemical compositions with sequential variations in plasma duty cycle were demonstrated in polymerization of both perfluoroalkane and vinyl acetic acid monomers. As anticipated, polymer films obtained from the perfluorocarbon monomers exhibited a general trend towards more linear structures with decreasing plasma duty cycles. However, completely unexpectedly, ultrahydrophobic films were obtained from some of these monomers under restricted duty cycle and power input conditions. SEM and XPS characterizations revealed that a rough, fibrous-like surface morphology is responsible for this ultrahydrophobicity, as opposed to unusual chemical compositions. The growth of the fibrous surface is believed to arise from nucleation and hillock-like growth patterns on selectively activated sites of the growing polymer film. Surface mobility of plasma generated reactive species apparently plays an important role in the growth of the fibrous ultrahydrophobic surfaces, as shown by substrate temperature studies. Additionally, the present study revealed a number of interesting new observations of significant differences in the chemical compositions and deposition rates of polymer films obtained from the diverse range of perfluorocarbon monomers employed in this work. The ultrahydrophobic fluorocarbon films discovered in this investigation were evaluated for use in several biomaterial applications. The results obtained show excellent marine antifouling properties for these surfaces, as documented in ocean testing experiments. These surfaces have also been shown to be useful in controlling protein and peptide surface adsorptions, as well as in the inflammatory

  17. Chemical Modification: an Effective Way of Avoiding the Collapse of SWNTs on Al Surface Revealed by Molecular Dynamics Simulations

    DEFF Research Database (Denmark)

    Xie, J.; Xue, Q. Z.; Yan, K. Y.

    2009-01-01

    The rapid collapse of intrinsic single-walled carbon nanotube (SWNT) on the aluminum surface is observed using molecular dynamics simulation. The collapsing threshold is similar to 10 angstrom, and the length has no influence on its collapse. Furthermore, we report that the structural stability...... of cylindrical SWNTs oil the aluminum surface can be improved through the surface modification method. The stability of SWNTs call be enhanced by increasing the modification coverage. When the modification coverage exceeds 3.3% and 3.8% coverage, respectively, both amidogen- and carboxyl-modified SWNTs can...... basically maintain the cylindrical structure in our described systems. The results also show that, to avoid SWNTs collapse by chemical modification, the longer and larger SWNTs are, the more modification coverage SWNTs require. and vice versa. Our method allows potentially used modified SWNTs...

  18. The Influence of Cationization on the Dyeing Performance of Cotton Fabrics with Direct Dyes

    Directory of Open Access Journals (Sweden)

    M. F. Shahin

    2015-08-01

    Full Text Available The effect of cationic modification of cotton fabrics, using cationic agent (Chromatech 9414 on direct dyeing characteristics was studied in this work. Cationization of cotton fabric at different conditions (pH, cationic agent concentration, temperature and time was investigated and the optimum conditions were determined . Nitrogen content of cotton samples pretreated with cationic agent was indicated. The results showed that increasing cationic agent concentration lead to higher nitrogen content on cotton fabric . The cationized cotton fabrics were dyed with two direct dyes (C.I. Direct Yellow 142 - C.I. Direct red 224 and the results were compared to untreated cotton fabrics. The parameters which may affect the dyeing process such as dye concn., addition of salt, time and temperature of dyeing were studied. The dyeing results illustrate that cationization improves the fabric dyeability compared to the uncationized cotton and the magnitude of increase in colour depth depends on the nitrogen content of the cationized cotton fabric .The results also refer to possibility of dyeing cationized cotton fabric with direct dyes without addition of electrolytes to give colour strength higher than that achieved on uncationized cotton using conventional dyeing method .Another important advantage of cationic treatment is in the saving of dye concn., energy ,dyeing time , rinse water and subsequently saving of waste water treatment , and finally minimizes the environmental pollution . The changes in surface morphology of fibres after cationization were identified by various methods such as wettability and scanning with the electron microscope. Different fastness properties were evaluated.

  19. Synthesis and chemical modification of polymeric resins for the treatment of cations and aromatic hydrocarbons in produced oily water; Sintese de modificacao quimica de resina polimerica e aplicacao na remocao de cations e hidrocarbonetos aromaticos presentes em agua produzida

    Energy Technology Data Exchange (ETDEWEB)

    Aversa, Thiago M.; Rodrigues, Monique F.; Vieira, Helida V.P.; Queiros, Yure G.C.; Lucas, Elizabete F. [Universidade Federal do Rio de Janeiro, Instituto de Macromoleculas, Lab. de Macromoleculas e Coloides na Industria do Petroleo, Rio de Janeiro, RJ (Brazil)], e-mail: thiagoaversa@ima.ufrj.br

    2011-07-01

    The use of chemically modified resins in oily water treatment process is not very developed yet. Because of this, this work suggests to study the styrene and divinylbenzene sulfonation effect on oil and grease, aniline and calcium removal from the water. The aniline, oils and greases belong to a class of toxic organic compounds, with the Brazilian maximum limits established for disposal in CONAMA 393/2007, while the calcium ions belong to the group of cations of alkaline earth metals which improve hardness to the water, may cause fouling as carbonates and sulfates form. By using sulfonated resins in oily water treatment it is possible to remove not only oils and greases but also calcium and aniline. These kinds of polar compounds are removed because of the cation exchange capacity of resin. (author)

  20. A study on the die steel surface modification by electron beam

    CERN Document Server

    Wu Ai Min; Zou Jian Xin; Hao Sheng Zhi; Dong Chuang; Zhang Ai Ming; Xu Tao

    2002-01-01

    A new surface modification technology-high current pulsed electron beam treatment method was applied to the surface of die steel to improve its properties. It has been shown that as a result of the HCPEB treatment, the most pronounced changes of the structure-phase state occur in the near-surface layers quenched from the liquid state, where the crystallization front velocity reaches its maximum. In these layers partial or complete dissolving of second phases and formation of over saturated solid solutions and ordered nano-sized structures may take place. This makes it possible to improve substantially the electrochemical and strength properties of the surface layer. The authors found that the thickness of remelt layer is about 10 mu m, and the sectional microhardness increased accompanied by the enhancement of the wear resistance of the material. After modification, the relative wear resistance of D2 steel have increased 5.63 times and that of H13 steel increased 11.76 times

  1. Microwave-Assisted Surface Modification of Metallocene Polyethylene for Improving Blood Compatibility

    Directory of Open Access Journals (Sweden)

    Hemanth Mohandas

    2013-01-01

    Full Text Available A wide number of polymers are being used for various medical applications. In this work, microwave-assisted surface modification of metallocene polyethylene (mPE was studied. FTIR analysis showed no significant changes in the chemical groups after treatment. Contact angle analysis revealed a decrease in contact angle of the treated samples insinuating increasing hydrophilicity and better biocompatibility. Qualitative analysis of treated samples using scanning electron microscope (SEM depicted increasing surface roughness and holes formation further corroborating the results. Coagulation assays performed for estimating prothrombin time (PT and activated partial thromboplastin time (APTT showed an increase in the clotting time which further confirmed the improved blood compatibility of the microwave-treated surfaces. Further, the extent of hemolysis in the treated sample was lower than the untreated one. Hence, microwave-assisted surface modification of mPE resulted in enhanced blood compatibility. Improved blood compatibility of mPE may be exploited for fabrication of artificial vascular prostheses, implants, and various blood contacting devices.

  2. A novel surface modification of carbon fiber for high-performance thermoplastic polyurethane composites

    Science.gov (United States)

    Zhang, Yuanyuan; Zhang, Yizhen; Liu, Yuan; Wang, Xinling; Yang, Bin

    2016-09-01

    Properties of carbon fiber (CF) reinforced composites depend largely on the interfacial bonding strength between fiber and the matrix. In the present work, CF was grafted by 4,4‧-diphenylmethane diisocyanate (MDI) molecules after electrochemical oxidation treatment. The existence of functional groups introduced to the fiber surface and the changes of surface roughness were confirmed by FTIR, AFM, XPS, SEM and Raman spectroscopy. To evaluate the possible applications of this surface modification of carbon fiber, we examined the mechanical properties as well as the friction and wear performance of pristine CF and MDI-CF reinforced thermoplastic polyurethane (TPU) composites with 5-30 wt.% fiber contents, and found that the mechanical properties of TPU composites were all significantly improved. It is remarkable that when fiber content was 30 wt.%, the tensile strength of TPU/MDI-CF was increased by 99.3%, which was greater than TPU/CF (53.2%), and the friction loss of TPU/MDI-CF was decreased by 49.09%. The results of DMA and SEM analysis indicated the positive effects of MDI modification on the interfacial bonding between fibers and matrix. We believed that this simple and effective method could be used to the development of surface modified carbon fiber for high-performance TPU.

  3. Surface-defect induced modifications in the optical properties of α-MnO2 nanorods

    Science.gov (United States)

    John, Reenu Elizabeth; Chandran, Anoop; Thomas, Marykutty; Jose, Joshy; George, K. C.

    2016-03-01

    The science of defect engineering via surface tuning opens a new route to modify the inherent properties of nanomaterials for advanced functional and practical applications. In this work, two independent synthesis methods (hydrothermal and co-precipitation) are adopted to fabricate α-MnO2 nanorods with different defect structures so as to understand the effect of surface modifications on their optical properties. The crystal structure and morphology of samples are investigated with the aid of X-ray diffraction (XRD) and high resolution transmission electron microscopy (HRTEM). Atomic composition calculated from energy dispersive spectroscopy (EDS) confirms non-stoichiometry of the samples. The surface properties and chemical environment are thoroughly studied using X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) analysis. Bond angle variance and bond valence sum are determined to validate distortions in the basic MnO6 octahedron. The surface studies indicate that the concentration of Jahn-Teller manganese (III) (Mn3+) ion in the samples differ from each other which results in their distinct properties. Band structure modifications due to Jahn-Teller distortion are examined with the aid of ultraviolet-visible (UV) reflectance and photoluminescence (PL) studies. The dual peaks obtained in derivative spectrum conflict the current concept on the bandgap energy of MnO2. These studies suggest that emission lines from the samples can be strongly modified by selectively varying their defect density.

  4. Plasma immersion ion implantation for the efficient surface modification of medical materials

    Energy Technology Data Exchange (ETDEWEB)

    Slabodchikov, Vladimir A., E-mail: dipis1991@mail.ru; Borisov, Dmitry P., E-mail: borengin@mail.ru; Kuznetsov, Vladimir M., E-mail: kuznetsov@rec.tsu.ru [National Research Tomsk State University, Tomsk, 634050 (Russian Federation)

    2015-10-27

    The paper reports on a new method of plasma immersion ion implantation for the surface modification of medical materials using the example of nickel-titanium (NiTi) alloys much used for manufacturing medical implants. The chemical composition and surface properties of NiTi alloys doped with silicon by conventional ion implantation and by the proposed plasma immersion method are compared. It is shown that the new plasma immersion method is more efficient than conventional ion beam treatment and provides Si implantation into NiTi surface layers through a depth of a hundred nanometers at low bias voltages (400 V) and temperatures (≤150°C) of the substrate. The research results suggest that the chemical composition and surface properties of materials required for medicine, e.g., NiTi alloys, can be successfully attained through modification by the proposed method of plasma immersion ion implantation and by other methods based on the proposed vacuum equipment without using any conventional ion beam treatment.

  5. Development of 3D PPF/DEF scaffolds using micro-stereolithography and surface modification.

    Science.gov (United States)

    Lan, Phung Xuan; Lee, Jin Woo; Seol, Young-Joon; Cho, Dong-Woo

    2009-01-01

    Poly(propylene fumarate) (PPF) is an ultraviolet-curable and biodegradable polymer with potential applications for bone regeneration. In this study, we designed and fabricated three-dimensional (3D) porous scaffolds based on a PPF polymer network using micro-stereolithography (MSTL). The 3D scaffold was well fabricated with a highly interconnected porous structure and porosity of 65%. These results provide a new scaffold fabrication method for tissue engineering. Surface modification is a commonly used and effective method for improving the surface characteristics of biomaterials without altering their bulk properties that avoids the expense and long time associated with the development of new biomaterials. Therefore, we examined surface modification of 3D scaffolds by applying accelerated biomimetic apatite and arginine-glycine-aspartic acid (RGD) peptide coating to promote cell behavior. The apatite coating uniformly covered the scaffold surface after immersion for 24 h in 5-fold simulated body fluid (5SBF) and then the RGD peptide was applied. Finally, the coated 3D scaffolds were seeded with MC3T3-E1 pre-osteoblasts and their biologic properties were evaluated using an MTS assay and histologic staining. We found that 3D PPF/diethyl fumarate (DEF) scaffolds fabricated with MSTL and biomimetic apatite coating can be potentially used in bone tissue engineering.

  6. Modification of gravitational redshift of x-ray burst produced by pulsar surface magnetoplasma

    Institute of Scientific and Technical Information of China (English)

    Zhu Jun; Ji Pei-Yong

    2008-01-01

    In this paper,the propagation of x-ray bursts in the magnetoplasma of pulsar magnetosphere is discussed.The electromagnetic interaction between x-ray bursts and magnetoplasma is described as some geometry.The electromagnetic effects of surface superstrong magnetic field and dynamic effects of outflowing magnetoplasma of pulsars are treated as an optical metric.The Gordon metric is introduced to represent the gravitational metric and optical metric.So the propagation of x-ray bursts in magnetoplasma of pulsars can be described as x-ray bursts transmitting in an effective space characterized by Gordon metric.The modification of gravitational redshift,attributed to the flowing magnetoplasma of pulsars,is obtained and it is shown that the modification is of redshift and can reach the same magnitude as the gravitational redshift for ordinary pulsars.

  7. Surface defect modification of ZnO quantum dots based on rare earth acetylacetonate and their impacts on optical performance

    Science.gov (United States)

    Wang, Lixi; Yang, Xiaojuan; Yang, Weimin; Zhang, Jing; Zhang, Qitu; Song, Bo; Wong, Chingping

    2017-03-01

    The surface defect modification has an important effect on the application of ZnO quantum dots, and it has gained much progress in recently years, propelled by the development of additives. Our research efforts are directed toward developing a new surface modification additive RE(AcAc)3 (RE = Ce, Dy, Tb) to achieve fine ZnO QDs and adjust their surface properties. RE(AcAc)3/ZnO QDs nanostructured materials have been designed and prepared, and particular emphasis has been given to the relation between the surface modification and optical properties. The effects of RE(III) acetylacetonate modification on the FT-IR, TEM images and photoluminescence (PL) spectra were investigated, and the surface defect modification principle and effect were discussed in details. The band gap (Eg) was also calculated to prove the surface modification effect. For the RE(AcAc)3/ZnO QDs complex materials, stable linkage occurs because of the affinity of sbnd COOH from acetylacetonate anionic ligand to zinc oxide surfaces, with attachment to the zinc oxide by hydrogen bonding between the protons of the hydroxyl groups on the surface of ZnO QDs and the π-system of acetylacetone.

  8. Microstructural evolution and surface properties of nanostructured Cu-based alloy by ultrasonic nanocrystalline surface modification technique

    Science.gov (United States)

    Amanov, Auezhan; Cho, In-Sik; Pyun, Young-Sik

    2016-12-01

    A nanostructured surface layer with a thickness of about 180 μm was successfully produced in Cu-based alloy using an ultrasonic nanocrystalline surface modification (UNSM) technique. Cu-based alloy was sintered onto low carbon steel using a powder metallurgy (P/M) method. Transmission electron microscope (TEM) characterization revealed that the severe plastic deformation introduced by UNSM technique resulted in nano-sized grains in the topmost surface layer and deformation twins. It was also found by atomic force microscope (AFM) observations that the UNSM technique provides a significant reduction in number of interconnected pores. The effectiveness of nanostructured surface layer on the tribological and micro-scratch properties of Cu-based alloy specimens was investigated using a ball-on-disk tribometer and micro-scratch tester, respectively. Results exhibited that the UNSM-treated specimen led to an improvement in tribological and micro-scratch properties compared to that of the sintered specimen, which may be attributed to the presence of nanostructured surface layer having an increase in surface hardness and reduction in surface roughness. The findings from this study are expected to be implemented to the automotive industry, in particular connected rod bearings and bushings in order to increase the efficiency and performance of internal combustion engines (ICEs).

  9. Non-textured laser modification of silica glass surface: Wettability control and flow channel formation

    Science.gov (United States)

    Aono, Yuko; Hirata, Atsushi; Tokura, Hitoshi

    2016-05-01

    Local wettability of silica glass surface is modified by infrared laser irradiation. The silica glass surface exhibits hydrophobic property in the presence of sbnd CF3 or sbnd (CH3)2 terminal functional groups, which are decomposed by thermal treatment, and degree of the decomposition depends on the applied heat. Laser irradiation can control the number of remaining func